TY - JOUR A1 - Martínez, E. A1 - Lejeune, N. A1 - Frechilla, J. A1 - Porta-Velilla, L. A1 - Forneau, E. A1 - Angurel, L. A. A1 - de la Fuente, G. F. A1 - Bonse, Jörn A1 - Silhanek, A. V. A1 - Badía-Majós, A. T1 - Laser engineered architectures for magnetic flux manipulation on superconducting Nb thin films N2 - Custom shaped magnetic flux guiding channels have been fabricated on superconducting Nb thin films by laser nanopatterning of their surface. Preferential pathways are defined by suitable combination of imprinted anisotropic pinning domains through laser-induced periodic surface structures (LIPSS). Generated by the selective energy deposition of femtosecond UV laser pulses, quasi-parallel ripple structures are formed under optimized irradiation conditions. On average, each domain is formed by grooves with a lateral period of 260–270 nm and a depth about 80 nm. By combination of scanning and transmission electron microscopy, magneto-optical imaging, and conductive atomic force microscopy techniques, we conclude that the boundaries of the LIPSS-covered domains play a prominent role in the magnetic flux diversion process within the film. This is confirmed by dedicated modeling of the flux dynamics, combined with the inversion of the magneto-optical signal. The created metasurfaces enable control of the flux penetration process at the microscale. KW - Laser-induced periodic surface structures (LIPSS) KW - Magnetic flux KW - Magneto-optical imaging (MOI) KW - Critical current density PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-611243 UR - https://www.sciencedirect.com/science/article/pii/S0169433224019287 DO - https://doi.org/10.1016/j.apsusc.2024.161214 SN - 1873-5584 (Online) SN - 0169-4332 (Print) VL - 679 SP - 1 EP - 12 PB - Elsevier AN - OPUS4-61124 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vollpracht, A. A1 - Thiel, C. A1 - Zhao, Z. A1 - Villagrán Zaccardi, Y. A. A1 - Cordoba, G. P. A1 - Gluth, Gregor A1 - Vanoutrive, H. A1 - Gruyaert, E. A1 - Kanellopoulos, A. A1 - Mi, R. A1 - De Belie, N. T1 - Carbonation of concrete with SCMs: a data analysis by RILEM TC 281-CCC N2 - The RILEM TC 281–CCC "Carbonation of concrete with supplementary cementitious materials" is studying the effect of supplementary cementitious materials (SCMs) on natural and accelerated carbonation of blended cements. In this context a large database with carbonation depths over time has been set-up with currently 910 concrete and mortar mixes, which have been tested at different curing conditions. The collected data includes information on chemical composition and physical properties of the raw materials, on mix-design, compressive strength, curing and carbonation testing conditions. Data for a large variety of binders (with up to 94 % SCMs) and mix designs (with w/b ratios ranging from 0.26 to 0.75) were collected from the literature and unpublished material testing projects. Natural carbonation was recorded for several years in many cases, and indoor as well as outdoor results are included. However, in this contribution only lab conditions are considered. Carbonation kinetics are investigated considering the binder composition and mix design. Furthermore, the accuracy of accelerated carbonation testing is evaluated. As described in literature, the w/CaOreactive-ratio is a decisive factor for carbonation resistance but curing and exposure conditions influence the results as well. Even with identical test conditions, the scatter is very large. T2 - 16th International Congress on the Chemistry of Cement 2023 (ICCC2023) CY - Bangkok, Thailand DA - 18.09.2023 KW - Carbonation KW - Supplemetary cementitious materials KW - Blended cement KW - Concrete PY - 2023 UR - https://www.iccc-online.org/fileadmin/gruppen/iccc/proceedings/ICCC16_2023_Vol_III.pdf VL - III SP - 360 EP - 363 PB - Thailand Concrete Association AN - OPUS4-58736 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Frechilla, A. A1 - Martínez, E. A1 - del Moral, J. A1 - López-Santos, C. A1 - Frechilla, J. A1 - Nuñez-Gálvez, F. A1 - López-Flores, V. A1 - de la Fuente, G.F. A1 - Hülagü, Deniz A1 - Bonse, Jörn A1 - González-Elipe, A.R. A1 - Borrás, A. A1 - Angurel, L.A. T1 - Influence of near-edge Laser-Induced Periodic Surface Structures (LIPSS) on the electrical properties of fs-laser-machined ITO microcircuits N2 - Scalable, cost-effective methods for processing transparent electrodes at the microscale are pivotal to advancing in electrochemistry, optoelectronics, microfluidics, and energy harvesting. In these fields, the precise fabrication of micrometric circuits and patterns plays a critical role in determining device performance, material compatibility, and integration with added-value substrates. In this context, Laser Subtractive Manufacturing stands out as a suitable microfabrication technique for its adaptability to diverse materials and complex configurations, as well as its straightforward scalability, affordability, and eco-friendly nature. However, a challenge in micromachining metals and metal oxides is the inherent formation of Laser-Induced Periodic Surface Structures (LIPSS), which can significantly impair electrical conductivity, particularly when circuit dimensions fall within the micrometer range. Herein, we investigate the micromachining of electrical microcircuits using ultrashort pulse laser systems applied to transparent indium tin oxide (ITO) thin films. We analyze the formation of LIPSS at the edges of the micromachined regions associated with the Gaussian distribution of the energy within the laser spot, and the impact of these structures on the electrical properties of the circuits. Thus, we systematically evaluate the influence of LIPSS orientation and periodicity by fabricating various circuit patterns using femtosecond lasers at green (515 nm) and ultraviolet (UV) (343 nm) wavelengths. A correlation between electrical resistivity measurements and microstructure analysis, as determined by field emission scanning electron and transmission electron microscopy, reveals distinct effects of the formed nanostructures depending on the laser source and its polarization. For the green wavelength, the edge side regions where LIPSS are oriented perpendicular to the ITO track exhibit a resistance higher by a factor just above two compared to those where LIPSS are parallel. Additionally, UV laser processing results in a pronounced reduction of ITO thickness at the boundary between the LIPSS region and the substrate. The mechanisms for the formation of LIPSS with both wavelengths are also discussed. Furthermore, we have determined that in narrow conductive tracks with a width ranging from 6 to 8 µm, the impact of LIPSS is particularly significant because the LIPSS structured region occupies a dominant fraction of the total width. KW - ITO KW - Laser-induced periodic surface structures (LIPSS) KW - Laser subtractive manufacturing KW - fs-laser processing KW - Electrical properties PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-655921 DO - https://doi.org/10.1016/j.apsusc.2026.166415 SN - 0169-4332 VL - 731 SP - 1 EP - 13 PB - Elsevier B.V. AN - OPUS4-65592 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Porta-Velilla, L. A1 - Turan, N. A1 - Cubero, Á. A1 - Shao, W. A1 - Li, H. A1 - de la Fuente, G.F. A1 - Martínez, E. A1 - Larrea, Á. A1 - Castro, M. A1 - Koralay, H. A1 - Çavdar, Ş. A1 - Bonse, Jörn A1 - Angurel, L.A. T1 - Highly Regular Hexagonally-Arranged Nanostructures on Ni-W Alloy Tapes upon Irradiation with Ultrashort UV Laser Pulses N2 - Nickel tungsten alloy tapes (Ni—5 at% W, 10 mm wide, 80 µm thick, biaxially textured) used in second-generation high temperature superconductor (2G-HTS) technology were laser-processed in air with ultraviolet ps-laser pulses (355 nm wavelength, 300 ps pulse duration, 250–800 kHz pulse repetition frequency). By employing optimized surface scan-processing strategies, various laser-generated periodic surface structures were generated on the tapes. Particularly, distinct surface microstructures and nanostructures were formed. These included sub-wavelength-sized highly-regular hexagonally-arranged nano-protrusions, wavelength-sized line-grating-like laser-induced periodic surface structures (LIPSS, ripples), and larger irregular pyramidal microstructures. The induced surface morphology was characterized in depth by electron-based techniques, including scanning electron microscopy (SEM), electron back scatter diffraction (EBSD), cross-sectional transmission electron microscopy (STEM/TEM) and energy dispersive X-ray spectrometry (EDS). The in-depth EBSD crystallographic analyses indicated a significant impact of the material initial grain orientation on the type of surface nanostructure and microstructure formed upon laser irradiation. Special emphasis was laid on high-resolution material analysis of the hexagonally-arranged nano-protrusions. Their formation mechanism is discussed on the basis of the interplay between electromagnetic scattering effects followed by hydrodynamic matter re-organization after the laser exposure. The temperature stability of the hexagonally-arranged nano-protrusion was explored in post-irradiation thermal annealing experiments, in order to qualify their suitability in 2G-HTS fabrication technology with initial steps deposition temperatures in the range of 773–873 K. KW - Laser-induced periodic surface structures (LIPSS) KW - Ultrashort laser processing KW - Hexagonally-arranged nano-protrusions KW - Second-generation high temperature superconductor technology KW - Electron microscopy PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-552551 DO - https://doi.org/10.3390/nano12142380 SN - 2079-4991 VL - 12 IS - 14 SP - 1 EP - 23 PB - MDPI CY - Basel, Switzerland AN - OPUS4-55255 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Reimold, W. U. A1 - Crosta, A. P. A1 - Hasch, M. A1 - Kowitz, Astrid A1 - Hauser, N. A1 - Sanchez, J. P. A1 - Simoes, L. S. A. A1 - de Sanchez, G. J. A1 - Zaag, P. T. T1 - Shock deformation confirms the impact origin for the Cerro do Jarau, Rio Grande do Sul, Brazil, structure N2 - Cerro do Jarau is a conspicuous, circular morpho‐structural feature in Rio Grande do Sul State (Brazil), with a central elevated core in the otherwise flat “Pampas” terrain typical for the border regions between Brazil and Uruguay. The structure has a diameter of approximately 13.5 km. It is centered at 30o12′S and 56o32′W and was formed on basaltic flows of the Cretaceous Serra Geral Formation, which is part of the Paraná‐Etendeka Large Igneous Province (LIP), and in sandstones of the Botucatu and Guará formations. The structure was first spotted on aerial photographs in the 1960s. Ever since, its origin has been debated, sometimes in terms of an endogenous (igneous) origin, sometimes as the result of an exogenous (meteorite impact) event. In recent years, a number of studies have been conducted in order to investigate its nature and origin. Although the results have indicated a possible impact origin, no conclusive evidence could be produced. The interpretation of an impact origin was mostly based on the morphological characteristics of the structure; geophysical data; as well as the occurrence of different breccia types; extensive deformation/silicification of the rocks within the structure, in particular the sandstones; and also on the widespread occurrence of low‐pressure deformation features, including some planar fractures (PFs). A detailed optical microscopic analysis of samples collected during a number of field campaigns since 2007 resulted in the disclosure of a large number of quartz grains from sandstone and monomict arenite breccia from the central part of the structure with PFs and feather features (FFs), as well as a number of quartz grains exhibiting planar deformation features (PDFs). While most of these latter grains only carry a single set of PDFs, we have observed several with two sets, and one grain with three sets of PDFs. Consequently, we here propose Cerro do Jarau as the seventh confirmed impact structure in Brazil. Cerro do Jarau, together with Vargeão Dome (Santa Catalina state) and Vista Alegre (Paraná State), is one of very few impact structures on Earth formed in basaltic rocks. KW - Serra da cangalha KW - Recovery experiments KW - Piaui state KW - Santa-marta KW - Features KW - Pressure KW - GPA KW - Sandstone KW - Geology PY - 2018 DO - https://doi.org/10.1111/maps.13233 SN - 1086-9379 VL - 54 IS - 10 SP - 2384 EP - 2394 PB - Wiley AN - OPUS4-50029 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jenning, M. A1 - Marklein, B. A1 - Ytterberg, J. A1 - Zubarev, R. A. A1 - Joshua, V. A1 - van Schaardenburg, D. A1 - van de Stadt, L. A1 - Catrina, A. I. A1 - Nonhoff, U. A1 - Häupl, T. A1 - Konthur, Zoltán A1 - Burmester, G. R. A1 - Skriner, K. T1 - Bacterial citrullinated epitopes generated by Porphyromonas gingivalis infection—a missing link for ACPA production N2 - Objectives: Porphyromonas gingivalis (P.g.) is discussed to be involved in triggering self-reactive immune responses. The aim of this study was to investigate the autocitrullinated prokaryotic peptidylarginine deiminase (PPAD) from P.g. CH2007 (RACH2007-PPAD) from a rheumatoid arthritis (RA) patient and a synthetic citrullinated PPAD peptide (CPP) containing the main autocitrullination site as potential targets for antibody reactivity in RA and to analyse the possibility of citrullinating native human proteins by PPAD in the context of RA. Methods: Recombinant RACH2007-PPAD was cloned and expressed in Escherichia coli. Purified RACH2007-PPAD and its enzymatic activity was analysed using two-dimensional electrophoresis, mass spectrometry, immunoblot and ELISA. Autoantibody response to different modified proteins and peptides was recorded and bioinformatically evaluated. Results: RACH2007-PPAD was capable to citrullinate major RA autoantigens, such as fibrinogen, vimentin, hnRNP-A2/B1, histone H1 and multiple peptides, which identify a common RG/RGG consensus motif. 33% of RA patients (n=30) revealed increased reactivity for α-cit-RACH2007-PPAD before RA onset. 77% of RA patients (n=99) presented α-cit-specific signals to CPP amino acids 57-71 which were positively correlated to α-CCP2 antibody levels. Interestingly, 48% of the α-CPP-positives were rheumatoidfactor IgM/anti-citrullinated peptide/protein antibodies (ACPA)-negative. Anti-CPP and α-RACH2007-PPAD antibody levels increase with age. Protein macroarrays that were citrullinated by RACH2007-PPAD and screened with RA patient sera (n=6) and controls (n=4) uncovered 16 RACH2007-PPAD citrullinated RA autoantigens and 9 autoantigens associated with lung diseases. We showed that the α-CPP response could be an important determinant in parenchymal changes in the lung at the time of RA diagnosis (n=106; p=0.018). Conclusions: RACH2007-PPAD induced internal citrullination of major RA autoantigens. Anti-RACH2007-PPAD correlates with ACPA levels and interstitial lung disease autoantigen reactivity, supporting an infection-based concept for induction of ACPAs via enzymatic mimicry. KW - Zitrullin KW - Rheumatoide Arthritis KW - Proteinmodifikation KW - Autoantikörper PY - 2020 DO - https://doi.org/10.1136/annrheumdis-2019-216919 VL - 79 IS - 9 SP - 1194 EP - 1202 PB - BMJ Publishing Group Ltd AN - OPUS4-51372 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Cros, A. A1 - Alfaro Espinoza, Gabriela A1 - De Maria, A. A1 - Wirth, N. T. A1 - Nikel, P. I. T1 - Synthetic metabolism for biohalogenation N2 - The pressing need for novel bioproduction approaches faces a limitation in the number and type of molecules accessed through synthetic biology. Halogenation is widely used for tuning physicochemical properties of molecules and polymers, but traditional halogenation chemistry often lacks specificity and generates harmful by-products. Here, we pose that deploying synthetic metabolism tailored for biohalogenation represents an unique opportunity towards economically attractive and environmentally friendly organohalide production. On this background, we discuss growth-coupled selection of functional metabolic modules that harness the rich repertoire of biosynthetic and biodegradation capabilities of environmental bacteria for in vivo biohalogenation. By rationally combining these approaches, the chemical landscape of Living cells can accommodate bioproduction of added-value organohalides which, as of today, are obtained by traditional chemistry. KW - Halogenation KW - Synthetic metabolism PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-542013 DO - https://doi.org/10.1016/j.copbio.2021.11.009 SN - 0958-1669 SN - 1879-0429 VL - 74 SP - 180 EP - 193 PB - Elsevier CY - Amsterdam AN - OPUS4-54201 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Porta-Velilla, L. A1 - Martínez, E. A1 - Frechilla, A. A1 - Castro, M. A1 - de la Fuente, G. F. A1 - Bonse, Jörn A1 - Angurel, L. A. T1 - Grain orientation, angle of incidence, and beam polarization effects on ultraviolet 300 ps-laser-induced nanostructures on 316L stainless steel N2 - Laser-induced periodic surface structures (LIPSS) represent a unique route for functionalizing materials through the fabrication of surface nanostructures. Commercial AISI 316L stainless steel (SS316L) surfaces are laser treated by ultraviolet 300 ps laser pulses in a laser line scanning (LLS) approach. Processing parameters are optimized (pulse energy of 2.08 µJ, pulse repetition frequency of 300 kHz, and suitable laser scan and sample displacement rates) for the generation of low spatial frequency LIPSS over a large 25 × 25 mm2 area. Different angles of incidence of the laser radiation (0°, 30°, and 45°) and different linear laser beam polarizations (s and p) produce a plethora of rippled surface morphologies at distinct grains. Scanning electron microscopy and 2D Fourier transforms, together with calculations of the optical energy deposited at the treated surfaces using Sipe's first-principles electromagnetic scattering theory, are used to study and analyze in detail these surface morphologies. Combined with electron backscattering diffraction, analyses allow associating site-selectively various laser-induced-surface morphologies with the underlying crystalline grain orientation. Resulting grain orientation maps reveal a strong impact of the grain crystallographic orientation on LIPSS formation and point toward possible strategies, like multi-step processes, for improving the manufacturing of LIPSS and their areal coverage of polycrystalline technical materials. KW - Laser-induced periodic surface structures (LIPSS) KW - Steel KW - Grain orientation KW - Electron backscattering diffraction (EBSD) KW - Laser processing PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-588929 DO - https://doi.org/10.1002/lpor.202300589 SN - 1863-8899 SP - 1 EP - 21 PB - Wiley-VCH GmbH CY - Weinheim AN - OPUS4-58892 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nanaki, E. A. A1 - Koroneos, C. J. A1 - Roset, J. A1 - Susca, Tiziana A1 - Christensen, T. H. A1 - De Gregorio Hurtado, S. A1 - Rybka, A. A1 - Kopitovic, J. A1 - Heindrich, O. A1 - Amparo Lopez-Jimenez, P. T1 - Environmental assessment of 9 European public bus transportation systems N2 - The transportation sector is one of the largest sources of EU’s greenhouse gas emissions. In 2011, trans-portation represented approximately 25 percent of total EU’s greenhouse gas emissions. Urban mobilityaccounts for 40 % of all CO2emissions of road transport and up to 70 % of other pollutants from transport.As, transportation and mobility play a crucial part both in urban economics and the quality of life, it is ofgreat significance to ensure a low carbon transportation sector, so as to deal with the threat that climatechange poses to urban areas. This study examines the factors that affect the production of carbon dioxide(CO2) as well as of air pollutants, in 9 major European cities, aiming to provide a comprehensive overviewof the actual knowledge on the atmospheric pollution from public transportation systems. CO2emissionsas well as air pollutants, such as CO, HC, PM, NOx are calculated for the diesel and CNG bus fleets of theEuropean cities under study. Finally the environmental benefits, in terms of CO2and CO, HC, PM, NOxemissions reductions, from the penetration of different biodiesel blends (from B10 to B100) to the busfleets are estimated. KW - Urban buses KW - Air pollution KW - Urban transport PY - 2017 DO - https://doi.org/10.1016/j.scs.2016.08.025 SN - 2210-6707 VL - 28 SP - 42 EP - 52 PB - Elsevier AN - OPUS4-38938 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Szymoniak, Paulina A1 - Kolmangadi, Mohamed A. A1 - Böhning, Martin A1 - Frick, B. A1 - Apple, M. A1 - Mole, R. A. A1 - De Souza, N. R. A1 - Zorn, R. A1 - Schönhals, Andreas T1 - Confined Segmental Diffusion in Nanophase Separated Janus Polynorbornenes as Investigated by Quasielastic Neutron Scattering N2 - A combination of neutron time-of-flight and neutron backscattering spectroscopy was used to investigate the molecular dynamics of Janus polynorbornenes (Janus poly(tricyclononenes)) on a microscopic level. These Janus polynorbornenes, denoted as PTCNSiOR, have a semirigid backbone with −Si(OR)3 side groups attached to it. R represents the length of the alkyl side chain. Here side chain lengths of R = 3 (propyl) and R = 8 (octyl) were considered. It is worth mentioning that these polymers have some potential as active layers in gas separation membranes, especially for the separation of higher hydrocarbons. The combination of time-of-flight and backscattering will ensure a reasonably broad time window for analysis where the incoherent intermediate scattering function SInc(q,t) is considered. Previously, it was shown by X-ray investigations that the system undergoes a nanophase separation into alkyl side chain-rich domains surrounded by a backbone-rich matrix. For PTCNSiOPr (R = 3), the alkyl side-chain-rich domains are truly isolated in the backbone-rich matrix, whereas for PTCNSiOOc (R = 8) these domains percolate through the matrix. Further, it was also previously shown that the alkyl side-chain-rich domains undergo a glass transition. The advantage of neutron scattering experiments discussed here is that besides temporal also spatial information is obtained which will allow conclusions to be drawn about the type of molecular fluctuations. At the lowest measured temperature, the decay in Sinc(q,t) is due to the methyl group rotation. The methyl group dynamics is analyzed in terms of a modified jump-diffusion in a 3-fold potential and yields to a reasonable fraction of hydrogens which contribute to the methyl group rotation. At higher temperatures, the decay in SInc(q,t) is due to both the methyl group rotation and the segmental dynamics in the alkyl side-chain-rich domains. The segmental diffusion is modeled by a sublinear diffusion. For the analysis of the scattering function SInc(q,t) of PTCNSiOPr an elastic scattering due to the immobilized backbone-rich matrix must be taken into account. The analysis reveals that the segmental dynamics is confined by the finite size of alkyl chain-rich domains and that it is intrinsically heterogeneous in nature. Both effects are more pronounced for PTCNSiOPr in comparison to those of PTCNSiOOc. KW - Polynorbornene KW - Quasielastic Neutron Scattering PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-608712 DO - https://doi.org/10.1021/acs.macromol.4c01045 SP - 1 EP - 14 PB - ACS Publications AN - OPUS4-60871 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Driessens, F. C. M. A1 - De Maeyer, E. A. P. A1 - Fernández, E. A1 - Boltong, M. G. A1 - Berger, Georg A1 - Verbeeck, R. M. H. A1 - Ginebra, M. P. A1 - Planell, J. A. T1 - Amorphous calcium phosphate cements and their transformation into calcium deficient hydroxyapatite KW - Zement KW - Kalzium-Phosphat PY - 1996 VL - 9 SP - 231 EP - 234 AN - OPUS4-704 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Syed, A.A. A1 - Pittner, Andreas A1 - Rethmeier, Michael A1 - De, A. T1 - Modeling of gas metal arc welding process using an analytically determined volumetric heat source N2 - High peak temperature and continuous deposition of electrode droplets in the weld puddle inhibit real-time monitoring of thermal cycles and bead dimensions in gas metal arc welding. A three-dimensional numerical heat transfer model is presented here to compute temperature field and bead dimensions considering a volumetric heat source to account for the transfer of arc energy into the weld pool. The heat source dimensions are analytically estimated as function of welding conditions and original joint geometry. The deposition of electrode material is modeled using deactivation and activation of discrete elements in a presumed V-groove joint geometry. The computed values of bead dimensions and thermal cycles are validated with the corresponding measured results. A comparison of the analytically estimated heat source dimensions and the corresponding numerically computed bead dimensions indicate that the former could rightly serve as the basis for conduction heat transfer based models of gas metal arc welding process. KW - Gas metal arc welding KW - Heat conduction KW - Volumetric heat source KW - Experimental validation PY - 2013 DO - https://doi.org/10.2355/isijinternational.53.698 SN - 0915-1559 SN - 1347-5460 VL - 53 IS - 4 SP - 698 EP - 703 PB - ISIJ AN - OPUS4-28074 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Driessens, F. C. M. A1 - Boltong, M. G. A1 - Fernández, E. A1 - Ginebra, M. P. A1 - Planell, J. A. A1 - Verbeeck, R. M. H. A1 - De Maeyer, E. A. P. A1 - Berger, Georg T1 - Amorphous calcium phosphate cements T2 - 5th World Biomaterials Congress CY - Toronto, Canada DA - 1996-05-29 KW - Kalzium Phosphat Zement, amorph. PY - 1996 VL - 2 SP - 346 CY - Toronto AN - OPUS4-673 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bender, R. A1 - Féron, D. A1 - Mills, D. A1 - Ritter, S. A1 - Bäßler, Ralph A1 - Bettge, Dirk A1 - de Graeve, I. A1 - Dugstad, A. A1 - Grassini, S. A1 - Hack, T. A1 - Halama, M. A1 - Han, E.-H. A1 - Harder, T. A1 - Hinds, G. A1 - Kittel, J. A1 - Krieg, R. A1 - Leygraf, C. A1 - Martinelli, L. A1 - Mol, A. A1 - Neff, D. A1 - Nilsson, J.-O. A1 - Odnevall, I. A1 - Paterson, S. A1 - Paul, S. A1 - Prošek, T. A1 - Raupach, M. A1 - Revilla, R. I. A1 - Ropital, F. A1 - Schweigart, H. A1 - Szala, E. A1 - Terryn, H. A1 - Tidblad, J. A1 - Virtanen, S. A1 - Volovitch, P. A1 - Watkinson, D. A1 - Wilms, M. A1 - Winning, G. A1 - Zheludkevich, M. T1 - Corrosion challenges towards a sustainable society N2 - A global transition towards more sustainable, affordable and reliable energy systems is being stimulated by the Paris Agreement and the United Nation's 2030 Agenda for Sustainable Development. This poses a challenge for the corrosion industry, as building climate‐resilient energy systems and infrastructures brings with it a long‐term direction, so as a result the long‐term behaviour of structural materials (mainly metals and alloys) becomes a major prospect. With this in mind “Corrosion Challenges Towards a Sustainable Society” presents a series of cases showing the importance of corrosion protection of metals and alloys in the development of energy production to further understand the science of corrosion, and bring the need for research and the consequences of corrosion into public and political focus. This includes emphasis on the limitation of greenhouse gas emissions, on the lifetime of infrastructures, implants, cultural heritage artefacts, and a variety of other topics. KW - Corrosion KW - Corrosion costs KW - Corrosion protection KW - Preventive strategies PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-554801 DO - https://doi.org/10.1002/maco.202213140 SN - 1521-4176 VL - 73 IS - 11 SP - 1730 EP - 1751 PB - Wiley-VCH CY - Weinheim AN - OPUS4-55480 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bäßler, Ralph A1 - Bettge, Dirk A1 - Bender, R. A1 - Féron, D. A1 - Mills, D. A1 - Ritter, S. A1 - de Graeve, I. A1 - Dugstad, A. A1 - Grassini, S. A1 - Hack, T. A1 - Halama, M. A1 - Han, E.-H. A1 - Harder, T. A1 - Hinds, G. A1 - Kittel, J. A1 - Krieg, R. A1 - Leygraf, C. A1 - Martinelli, L. A1 - Mol, A. A1 - Neff, D. A1 - Nilsson, J.-O. A1 - Odnevall, I. A1 - Paterson, S. A1 - Paul, S. A1 - Prosek, T. A1 - Raupach, M. A1 - Revilla, R. I. A1 - Ropital, F. A1 - Schweigart, H. A1 - Szala, E. A1 - Therryn, H. A1 - Tidblad, J. A1 - Virtanen, S. A1 - Volovitch, P. A1 - Watkinson, D. A1 - Wilms, M. A1 - Winning, G. A1 - Zheludkevich, M. T1 - La corrosion: un défi pour une société durable N2 - Une transition mondiale vers des systèmes énergétiques plus durables, abordables et fiables a été initiée par l’accord de Paris et l’Agenda 2030 des Nations unies pour un développement durable. Il s’agit là d’un défi industriel majeur car les systèmes et infrastructures énergétiques résilients au changement climatique exigent de se positionner pour le long terme. Se pencher sur le comportement dans la durée des matériaux structurels - principalement des métaux et des alliages - s’impose alors comme une nécessité. Dans cette optique, « La corrosion : un défi pour une société durable »présente une série de cas montrant l’importance de la tenue à la corrosion et de la protection anticorrosion des métaux et des alliages pour le développement de systèmes durables, économiques et fiables de production d’énergie. KW - Corrosion KW - Coûts de la corrosion KW - Protection KW - Anticorrosion KW - Stratégies deprévention PY - 2023 DO - https://doi.org/10.51257/a-v1-cor2000 SN - 2555-5383 VL - 2023 IS - Avril SP - 1 EP - 23 CY - Saint-Denis, France AN - OPUS4-57927 LA - fra AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - de Vallée, A. A1 - Bally, P. A1 - Bruel, C. A1 - Chandat, L. A1 - Choquer, M. A1 - Dieryckx, C. A1 - Dupuy, J.W. A1 - Kaiser, S. A1 - Latorse, M.-P. A1 - Loisel, E. A1 - Mey, G. A1 - Morgant, G. A1 - Rascle, C. A1 - Schumacher, Julia A1 - Simon, A. A1 - Souibgui, E. A1 - Viaud, M. A1 - Villalba, F. A1 - Poussereau, N. T1 - A similar secretome disturbance as a hallmark of non-pathogenic Botrytis cinerea ATMT-mutants? N2 - The gray mold fungus Botrytis cinerea is a necrotrophic pathogen able to infect hundreds of host plants, including high-value crops such as grapevine, strawberry and tomato. In order to decipher its infectious strategy, a library of 2,144 mutants was generated by random insertional mutagenesis using Agrobacterium tumefaciensmediated transformation (ATMT). Twelve mutants exhibiting total loss of virulence toward different host plants were chosen for detailed analyses. Their molecular characterization revealed a single T-DNA insertion in different loci. Using a proteomics approach, the secretome of four of these strains was compared to that of the parental strain and a common profile of reduced lytic enzymes was recorded. Significant variations in this profile, notably deficiencies in the secretion of proteases and hemicellulases, were observed and validated by biochemical tests. They were also a hallmark of the remaining eight non-pathogenic strains, suggesting the importance of these secreted Proteins in the infection process. In the twelve non-pathogenic mutants, the Differentiation of infection cushions was also impaired, suggesting a link between the Penetration structures and the secretion of proteins involved in the virulence of the pathogen. KW - Fungus KW - Plant pathogen KW - Virulence PY - 2019 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-502710 DO - https://doi.org/10.3389/fmicb.2019.02829 SN - 1664-302X VL - 10 SP - Article 2829 PB - Frontiers Media CY - Lausanne AN - OPUS4-50271 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Deroubaix, G. A1 - Labat, G. A1 - Lebayon, I. A1 - Legay, S. A1 - Marchal, P. A1 - Yrieix, C. A1 - Melcher, E. A1 - Peek, R.-D. A1 - De Geyter, S. A1 - van Acker, J. A1 - Homan, W. A1 - Dickinson, D. A1 - Murphy, R. A1 - Suttie, E. A1 - Nurmi, A. A1 - Ritschkoff, A. A1 - Rudolph, Dieter A1 - Stephan, Ina A1 - Aston, D. A1 - Baines, E. A1 - Simonin, J. T1 - Environmental Risk Assessment of Treated Timber in Service - the Environment Focus Group Approach N2 - In the context of the Biocidal Products Directive (98/8/EC), and of the OECD work on wood preservatives, the Environment Focus Group (EFG), comprising 8 institutes and the European Wood Preservative Manufacturers Group, has been working on the environmental risk assessment of treated timber in service. A literature review of emissions from treated timber has revealed that very little existing data is usable for environmental risk assessment; the most relevant data are kinetic curves of emissions over time, which show clearly the non-linear emissions behaviour of treated wood over time. The EFG has suggested real exposure conditions for treated timber in the environment, and listed typical exposure scenarios. Five representative scenarios are characterised in detail, for use in the calculation of Predicted Environmental Concentrations (PECs). The existing methods to determine emissions from treated wood have been reviewed. Most existing experimental models cannot be used to predict environmental emissions. Monitoring of commodities in service has its specific constraints. Chemical analysis and ecotoxicity testing have also been reviewed and their relationship has been discussed. Principles for the design of experimental models, for the determination of emission fluxes from treated wood to the environment, have been established. T2 - 31th Annual Meeting of the International Research Group on Wood Preservation CY - Kona, HI, USA DA - 2000-05-14 PY - 2000 UR - http://www.irg-wp.com/irgdocs/details.aspx?id=42bc629a-609f-4689-8a62-3542121b4a79 SP - Paper 50162, 1 EP - 17 PB - International Research Group on Wood Preservation CY - Stockholm AN - OPUS4-4455 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gao, S. A1 - Hou, J. A1 - Deng, Z. A1 - Wang, T. A1 - Beyer, Sebastian A1 - de Oliveira Guilherme Buzanich, Ana A1 - Richardson, J. J. A1 - Rawal, A. A1 - Seidel, R. A1 - Zulkifli, M. Y. A1 - Li, W. A1 - Bennett, T. D. A1 - Cheetham, A. K. A1 - Liang, K. T1 - Improving the Acidic Stability of Zeolitic Imidazolate Frameworks by Biofunctional Molecules N2 - Zeolitic imidazolate frameworks (ZIFs) have been widely investigated for their use in separation, gas adsorption, catalysis, and biotechnology. Their practical applications, however, can be hampered by their structural instability in humid acidic conditions. Here, guided by density functional theory calculations, we demonstrate that the acidic stability of two polymorphic ZIFs (i.e., ZIF-8 and ZIF-L) can be enhanced by the incorporation of functional groups on polypeptides or DNA. A range of complementary synchrotron investigations into the local chemical structure and bonding environment suggest that the enhanced acidic stability arises from the newly established coordinative interactions between the Zn centers and the inserted carboxylate (for polypeptides) or phosphate (for DNA) groups, both of which have lower pKas than the imidazolate ligand. With functional biomolecular homologs (i.e., enzymes), we demonstrate a symbiotic stability reinforcement effect, i.e., the encapsulated biomolecules stabilize the ZIF matrix while the ZIF exoskeleton protects the enzyme from denaturation. KW - Zeolitic Imidazolate Frameworks KW - Biofunctional Molecules KW - X-ray Absorption Spectroscopy PY - 2019 DO - https://doi.org/10.1016/j.chempr.2019.03.025 VL - 5 IS - 6 SP - 1597 EP - 1608 PB - Elsevier Inc. AN - OPUS4-48702 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wintzheimer, S. A1 - Szczerba, Wojciech A1 - de Oliveira Guilherme Buzanich, Ana A1 - Kashiwaya, S. A1 - Klein, A. A1 - Jaegermann, W. A1 - Toupance, T. A1 - Shmeliov, A. A1 - Nicolosi, V. A1 - Heuzé, K. A1 - Mandel, K. A1 - Dembski, S. T1 - Discovering the determining parameters for the photocatalytic activity of TiO2 colloids based on an anomalous dependence on the specific surface area N2 - The photocatalytic (PC) performance of titanium dioxide (TiO2) nanoparticles strongly depends on their specific surface, the presence of crystal defects, their crystal phase, and the exposed crystal facets. In order to understand which of these factors contributes most significantly to the PC activity of TiO2 colloids, all of them have to be individually analyzed. This study entails the synthesis of five anatase nanocrystal samples. By maintaining the same reactant ratios as well as hydrothermal sol–gel synthesis route and only varying the autoclaving time or temperature, different crystallite sizes are obtained under comparable experimental conditions. A decrease in PC performance with increase in specific surface area is found. Such an unexpected counterintuitive result establishes the basis for a better understanding of the crucial factors that ultimately determine the PC activity. These are investigated by studying nanocrystals bulk and surface structure and morphology using a selection of complementary analysis methods (X-ray photoelectron spectroscopy (XPS), X-ray absorption fine structure (XAFS), X-ray diffraction (XRD)…). It is found that a change in the nanocrystal morphology from an equilibrium state truncated tetragonal bipyramid to a more elongated rod-like structure accompanied by an increase in oxygen vacancies is responsible for an augmented PC activity of the TiO2 nanocrystals. KW - Ti-based colloids KW - Photocatalysis KW - Spectroscopy KW - XAFS PY - 2018 DO - https://doi.org/10.1002/ppsc.201800216 SN - 0934-0866 SN - 1521-4117 VL - 35 IS - 9 SP - 1800216, 1 EP - 10 PB - Wiley Online Library AN - OPUS4-46068 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - INPR A1 - Liu, Yanchen A1 - de Oliveira Guilherme Buzanich, Ana A1 - Alippi, Paola A1 - Lee, Kug-Seung A1 - Jeon, Taeyeol A1 - Weißer, Kilian A1 - Karlsen, Martin A. A1 - Russo, Patrícia A. A1 - Pinna, Nicola T1 - FeNb2O6 as a high-performance anode for sodium-ion batteries enabled by structural amorphization coupled with NbO6 local ordering. N2 - Pseudocapacitance-type transition metal oxides have been extensively investigated as anodes materials for lithium-ion batteries. Currently, they are also emerging as promising anodes for sodium-ion batteries due to their low volume change and safety. However, the potential electrochemical performance in sodium energy storage is not fully achieved, primarily due to the larger radius of the Na+-ions. Here, we report for the first time an iron niobate with columbite structure as a high-performance sodium storage anode. The presence of iron in the structure is vital to trigger the loss of long-range order through disorder of the FeO6 octahedra local structure, subsequently allowing reversible Na storage in an amorphous phase. Simultaneously, the formation of short-range ordered zigzag-chain structures within the NbO6 planes creates a “skeleton” that offers abundant active sites for pseudocapacitive ion storage and enhanced ion diffusion pathways. These characteristics of FeNb2O6 make it an effective intercalation host, offering high capacity along with fast Na+ insertion and extraction, as demonstrated through operando and ex-situ characterizations. It leads to an applicable reversible capacity ( 300 mAh g-1) with a favorable average voltage of ca. 0.6 V and excellent rate capability (180.4 mAh g-1 at a current density of 2 A g-1). This study provides insights into the development of intrinsically active transition metal oxides for Na+-ion intercalation. KW - XAS KW - Sodium-Ion-Batteries KW - In-situ PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-631159 DO - https://doi.org/10.26434/chemrxiv-2025-2gn7z SP - 1 EP - 51 PB - American Chemical Society (ACS) AN - OPUS4-63115 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Smekhova, A. A1 - Kuzmin, A. A1 - Siemensmeyer, K. A1 - Abrudan, R. A1 - Reinholz, Uwe A1 - de Oliveira Guilherme Buzanich, Ana A1 - Schneider, M. A1 - Laplanche, G. A1 - Yusenko, Kirill T1 - Inner relaxations in equiatomic single-phase high-entropy Cantoralloy N2 - The superior properties of high-entropy multi-functional materials are strongly connected with their atomic heterogeneity through many different local atomic interactions. The detailed element-specific studies on a local scale can provide insight into the primary arrangements of atoms in multicomponent systems and benefit to unravel the role of individual components in certain macroscopic properties of complex compounds. Herein, multi-edge X-ray absorption spectroscopy combined with reverse Monte Carlo simulations was used to explore a homogeneity of the local crystallographic ordering and specific structure relaxations of each constituent in the equiatomic single-phase facecentered cubic CrMnFeCoNi high-entropy alloy at room temperature. Within the considered fitting approach, all five elements of the alloy were found to be distributed at the nodes of the fcc lattice without any signatures of the additional phases at the atomic scale and exhibit very close statistically averaged interatomic distances (2.54 – 2.55 Å) with their nearest-neighbors. Enlarged structural displacements were found solely for Cr atoms. The macroscopic magnetic properties probed by conventional magnetometry demonstrate no opening of the hysteresis loops at 5 K and illustrate a complex character of the long-range magnetic order after field-assisted cooling in ± 5 T. The observed magnetic behavior is assigned to effects related to structural relaxations of Cr. Besides, the advantages and limitations of the reverse Monte Carlo approach to studies of multicomponent systems like high-entropy alloys are highlighted. KW - Magnetism KW - High-entropy alloys KW - Reverse Monte Carlo (RMC) KW - Element-specific spectroscopy KW - Extended X-ray absorption fine structure (EXAFS) KW - X-ray absorption near edge structure (XANES) PY - 2022 DO - https://doi.org/10.1016/j.jallcom.2022.165999 SN - 0925-8388 VL - 920 SP - 1 EP - 31 PB - Elsevier AN - OPUS4-55457 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Durlo Tambara, Luís Urbano A1 - Lima, G. T. S. A1 - Silvestro, L. A1 - Ruviaro, A. S. A1 - Gleize, P. J. P. A1 - de Azevedo, A. R. G. T1 - Influence of polycarboxylate superplasticizer and calcium sulfoaluminate cement on the rheology, hydration kinetics, and porosity of Portland cement pastes N2 - Binary systems composed of Portland cement (PC) and calcium sulfoaluminate (CSA) cement have stood out for applications requiring high early strengths. Nevertheless, the application of these systems may be limited due to their properties in the fresh state, which requires a better understanding of the rheological behavior of these materials. Thus, this study evaluated the incorporation of different polycarboxylate-based superplasticizer (SP) contents (0.15, 0.20, and 0.25 wt%) on PC and PC-CSA binary cement pastes. Rotational rheometry, isothermal calorimetry, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and nitrogen adsorption and desorption tests to assess the pore size distribution of cement pastes were conducted. While the SP incorporation reduced the dynamic yield stress of PC pastes, it progressively increased the yield stress of PC-CSA systems. The increase in SP content increased the main heat flow peak of PC-CSA pastes, although it did not significantly affect the cumulative heat after 160 h of hydration. FTIR and XRD confirm higher ettringite contents in the binary systems and indicate the presence of carboaluminates phases after 7 d of hydration in both PC and PC-CSA and hemicarboaluminate in PC-CSA pastes. The CSA incorporation reduced the cumulative pore volume by up to 32% compared to PC pastes, while the SP content evaluated did not significantly affect the porosity of PC-CSA pastes. KW - Calcium sulfoaluminate cement KW - Portland cement KW - Superplasticizer KW - Rheology KW - Hydration PY - 2023 DO - https://doi.org/10.1016/j.jobe.2023.106120 SN - 2352-7102 VL - 68 SP - 1 EP - 15 PB - Elsevier Ltd. CY - Amsterdam AN - OPUS4-57034 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rauwolf, M. A1 - Turyanskaya, A. A1 - Roschger, A. A1 - Prost, J. A1 - Simon, R. A1 - Scharf, O. A1 - Radtke, Martin A1 - Schoonjans, Tom A1 - de Oliveira Guilherme Buzanich, Ana A1 - Klaushofer, K. A1 - Wobrauschek, P. A1 - Hofstaetter, J. G. A1 - Roschger, P. A1 - Streli, C. T1 - Synchrotron radiation micro X-ray fluorescence spectroscopy of thin structures in bone samples: comparison of confocal and color X-ray camera setups N2 - In the quest for finding the ideal synchrotron-radiation-induced imaging method for the investigation of trace element distributions in human bone samples, experiments were performed using both a scanning confocal synchrotron radiation micro X-ray fluorescence (SR-mXRF) (FLUO beamline at ANKA) setup and a full-field color X-ray camera (BAMline at BESSY-II) setup. As zinc is a trace element of special interest in bone, the setups were optimized for its detection. The setups were compared with respect to count rate, required measurement time and spatial resolution. It was demonstrated that the ideal method depends on the element of interest. Although for Ca (a major constituent of the bone with a low energy of 3.69 keV for its K alpha XRF line) the color X-ray camera provided a higher resolution in the plane, for Zn (a trace element in bone) only the confocal SR-µXRF setup was able to sufficiently image the distribution. KW - Synchrotron KW - BAMline KW - BESSY KW - XRF KW - X-ray Color Camera PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-391944 DO - https://doi.org/10.1107/S1600577516017057 SN - 1600-5775 VL - 24 SP - 307 EP - 311 PB - International Union of Crystallography AN - OPUS4-39194 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bernal, S. A. A1 - Dhandapani, Y. A1 - Elakneswaran, Y. A1 - Gluth, Gregor A1 - Gruyaert, E. A1 - Juenger, M. C. G. A1 - Lothenbach, B. A1 - Olonade, K. A. A1 - Sakoparnig, M. A1 - Shi, Z. A1 - Thiel, C. A1 - Van den Heede, P. A1 - Vanoutrive, H. A1 - von Greve-Dierfeld, S. A1 - De Belie, N. A1 - Provis, J. L. T1 - Report of RILEM TC 281-CCC: A critical review of the standardised testing methods to determine carbonation resistance of concrete N2 - The chemical reaction between CO2 and a blended Portland cement concrete, referred to as carbonation, can lead to reduced performance, particularly when concrete is exposed to elevated levels of CO2 (i.e., accelerated carbonation conditions). When slight changes in concrete mix designs or testing conditions are adopted, conflicting carbonation results are often reported. The RILEM TC 281-CCC ‘Carbonation of Concrete with Supplementary Cementitious Materials’ has conducted a critical analysis of the standardised testing methodologies that are currently applied to determine carbonation resistance of concrete in different regions. There are at least 17 different standards or recommendations being actively used for this purpose, with significant differences in sample curing, pre-conditioning, carbonation exposure conditions, and methods used for determination of carbonation depth after exposure. These differences strongly influence the carbonation depths recorded and the carbonation coefficient values calculated. Considering the importance of accurately determining carbonation potential of concrete, not just for predicting their durability performance, but also for determining the amount of CO2 that concrete can re-absorb during or after its service life, it is imperative to recognise the applicability and limitations of the results obtained from different tests. This will enable researchers and practitioners to adopt the most appropriate testing methodologies to evaluate carbonation resistance, depending on the purpose of the conclusions derived from such testing (e. g. materials selection, service life prediction, CO2 capture potential). KW - Concrete KW - Cement KW - Carbonation KW - Testing KW - Standards PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-609364 DO - https://doi.org/10.1617/s11527-024-02424-9 VL - 57 SP - 1 EP - 31 PB - Springer Nature AN - OPUS4-60936 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Smekhova, A. A1 - Kuzmin, A. A1 - Siemensmeyer, K. A1 - Luo, C. A1 - Chen, K. A1 - Radu, F. A1 - Weschke, E. A1 - Reinholz, Uwe A1 - de Oliveira Guilherme Buzanich, Ana A1 - Yusenko, Kirill T1 - Al-driven peculiarities of local coordination and magnetic properties in single-phase Alx-CrFeCoNi high-entropy alloys N2 - Modern design of superior multi-functional alloys composed of several principal components requires in-depth studies of their local structure for developing desired macroscopic properties. Herein, peculiarities of atomic arrangements on the local scale and electronic states of constituent elements in the single-phase face-centered cubic (fcc)- and body-centered cubic (bcc)-structured high-entropy Alx-CrFeCoNi alloys (x = 0.3 and 3, respectively) are explored by element-specific X-ray absorption spectroscopy in hard and soft X-ray energy ranges. Simulations based on the reverse Monte Carlo approach allow to perform a simultaneous fit of extended X-ray absorption fine structure spectra recorded at K absorption edges of each 3d constituent and to reconstruct the local environment within the first coordination shells of absorbers with high precision. The revealed unimodal and bimodal distributions of all five elements are in agreement with structure-dependent magnetic properties of studied alloys probed by magnetometry. A degree of surface atoms oxidation uncovered by soft X-rays suggests different kinetics of oxide formation for each type of constituents and has to be taken into account. X-ray magnetic circular dichroism technique employed at L2,3 absorption edges of transition metals demonstrates reduced magnetic moments of 3d metal constituents in the sub-Surface region of in situ cleaned fcc-structured Al0.3-CrFeCoNi compared to their bulk values. Extended to nanostructured versions of multicomponent alloys, such studies would bring new insights related to effects of high entropy mixing on low dimensions. KW - X-ray magnetic circular dichroism (XMCD) KW - High-entropy alloys KW - Reverse Monte Carlo KW - Magnetism KW - Element-specific spectroscopy KW - Extended X-ray absorption fine structure (EXAFS) PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-530668 DO - https://doi.org/10.1007/s12274-021-3704-5 SN - 1998-0124 VL - 15 IS - 6 SP - 4845 EP - 4858 PB - Springer AN - OPUS4-53066 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vollpracht, A. A1 - Gluth, Gregor A1 - Rogiers, B. A1 - Uwanuakwa, I. D. A1 - Phung, Q. T. A1 - Villagran Zaccardi, Y. A1 - Thiel, C. A1 - Vanoutrive, H. A1 - Etcheverry, J. M. A1 - Gruyaert, E. A1 - Kamali-Bernard, S. A1 - Kanellopoulos, A. A1 - Zhao, Z. A1 - Martins, I. M. A1 - Rathnarajan, S. A1 - De Belie, N. T1 - Report of RILEM TC 281-CCC: insights into factors affecting the carbonation rate of concrete with SCMs revealed from data mining and machine learning approaches N2 - The RILEM TC 281–CCC ‘‘Carbonation of concrete with supplementary cementitious materials’’ conducted a study on the effects of supplementary cementitious materials (SCMs) on the carbonation rate of blended cement concretes and mortars. In this context, a comprehensive database has been established, consisting of 1044 concrete and mortar mixes with their associated carbonation depth data over time. The dataset comprises mix designs with a large variety of binders with up to 94% SCMs, collected from the literature as well as unpublished testing reports. The data includes chemical composition and physical properties of the raw materials, mix-designs, compressive strengths, curing and carbonation testing conditions. Natural carbonation was recorded for several years in many cases with both indoor and outdoor results. The database has been analysed to investigate the effects of binder composition and mix design, curing and preconditioning, and relative humidity on the carbonation rate. Furthermore, the accuracy of accelerated carbonation testing as well as possible correlations between compressive strength and carbonation resistance were evaluated. One approach to summerise the physical and chemical resistance in one parameter is the ratio of water content to content of carbonatable CaO (w/CaOreactive ratio). The analysis revealed that the w/CaOreactive ratio is a decisive factor for carbonation resistance, while curing and exposure conditions also influence carbonation. Under natural exposure conditions, the carbonation data exhibit significant variations. Nevertheless, probabilistic inference suggests that both accelerated and natural carbonation processes follow a square-root-of-time behavior, though accelerated and natural carbonation cannot be converted into each other without corrections. Additionally, a machine learning technique was employed to assess the influence of parameters governing the carbonation progress in concretes. KW - Carbonation KW - Supplementary cementitious materials KW - Concrete PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-614388 DO - https://doi.org/10.1617/s11527-024-02465-0 SN - 1871-6873 SN - 1359-5997 VL - 57 IS - 9 SP - 1 EP - 33 PB - Springer Nature AN - OPUS4-61438 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Liu, Yanchen A1 - de Oliveira Guilherme Buzanich, Ana A1 - Montoro, Luciano A. A1 - Liu, Hao A1 - Liu, Ye A1 - Emmerling, Franziska A1 - Russo, Patrícia A. A1 - Pinna, Nicola T1 - A partially disordered crystallographic shear block structure as fast-charging negative electrode material for lithium-ion batteries N2 - A well-ordered crystalline structure is crucial in battery electrodes, as the dimensionality and connectivity of the interstitial sites inherently influence Li+ ions diffusion kinetics. Niobium tungsten oxides block structures, composed of ReO3-type blocks of specific sizes with well-defined metal sites, are promising fast-charging negative electrode materials. Structural disorder is generally detrimental to conductivity or ion transport. However, here, we report an anomalous partially disordered Nb12WO33 structure that significantly enhances Li-ion storage performance compared to the known monoclinic Nb12WO33 phase. The partially disordered phase consists of corner-shared NbO6 octahedra blocks of varied sizes, including 5×4, 4×4, and 4×3, with a disordered arrangement of distorted WO4 tetrahedra at the corners of the blocks. This structural arrangement is robust during lithiation/delithiation, exhibiting minor local structure changes during cycling. It enables accelerated Li-ion migration, resulting in promising fast-charging performance, namely, 62.5 % and 44.7 % capacity retention at 20 C and 80 C, respectively. This study highlights the benefits of introducing disorder into niobium tungsten oxide shear structures, through the establishment of clear structure-performance correlations, offering guidelines for designing materials with targeted properties. KW - Lithium ion batteries KW - Oxides KW - XANES KW - XRD PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-637994 DO - https://doi.org/10.1038/s41467-025-61646-9 SN - 2041-1723 VL - 16 IS - 1 SP - 1 EP - 15 PB - Springer Science and Business Media LLC AN - OPUS4-63799 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Richter, Matthias A1 - Baldan, A. A1 - Beelen, R. A1 - de Boed, E. J.J. A1 - Tuma, Dirk A1 - Kipphardt, Heinrich A1 - Wilke, Olaf A1 - van der Veen, A. M.H. T1 - Primary gas standards for the determination of sulfur-based impurities at trace level in hydrogen N2 - Hydrogen fuel quality needs to comply with ISO 14687:2025 to avoid harmful impact on applications using proton-exchange membrane (PEM) fuel cells. For total sulfur as one of the most impactful contaminants, an amount fraction of 4 nmol/mol has been set as threshold (so-called Grade D quality). In this study, novel gaseous primary gas standards (PGS) of seven sulfur compounds were prepared either gravimetrically at 1000 nmol/mol, 100 nmol/mol, and 10 nmol/mol, or dynamically diluted down to 4 nmol/mol in hydrogen and argon matrices with relative expanded uncertainties well below 10 % (k = 2) and proven stability of at least 9–12 months. Two different cylinder passivation treatments were compared, with one treatment identified as unsuitable since reactions took place within the mixture. By performing a cross-check study, equivalence between both sets of PGS could be demonstrated (≤ 5 % relative deviation for most of the sulfur species). KW - Hydrogen quality KW - ISO 14687 KW - Sulfur impurities KW - Primary gas standards KW - TD-GC/SCD PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-656759 DO - https://doi.org/10.1016/j.ijhydene.2026.154461 SN - 0360-3199 VL - 224 SP - 1 EP - 13 PB - Elsevier Ltd. AN - OPUS4-65675 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Cubero, A. A1 - Martínez, E. A1 - Angurel, L.A. A1 - de la Fuente, G.F. A1 - Navarro, R. A1 - Legall, Herbert A1 - Krüger, Jörg A1 - Bonse, Jörn T1 - Effects of laser-induced periodic surface structures on the superconducting properties of Niobium N2 - It is well known that the use of ultrashort (fs) pulsed lasers can induce the generation of (quasi-) periodic nanostructures (LIPSS, ripples) on the surface of many materials. Such nanostructures have also been observed in sample’s surfaces irradiated with UV lasers with a pulse duration of 300 ps. In this work, we compare the characteristics of these nanostructures on 1-mm and on 25-μm thick niobium sheets induced by 30 fs n-IR and 300 ps UV pulsed lasers. In addition to conventional continuous or burst mode processing configurations, two-dimensional laser beam and line scanning modes have been investigated in this work. The latter allows the processing of large areas with a more uniform distribution of nanostructures at the surface. The influence of the generated nanostructures on the superconducting properties of niobium has also been explored. For this aim, magnetic hysteresis loops have been measured at different cryogenic temperatures to analyse how these laser treatments affect the flux pinning behaviour and, in consequence, the superconductor’s critical current values. It was observed that laser treatments are able to modify the superconducting properties of niobium samples. T2 - E-MRS Spring Meeting 2019 CY - Nice, France DA - 27.05.2019 KW - Superconductivity KW - Laser-induced periodic surface structures (LIPSS) KW - Niobium PY - 2020 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-502541 DO - https://doi.org/10.1016/j.apsusc.2019.145140 SN - 0169-4332 SN - 1873-5584 VL - 508 IS - 1 SP - 145140-1 EP - 145140-7 PB - Elsevier CY - Amsterdam AN - OPUS4-50254 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Cubero, A. A1 - Martínez, E. A1 - Angurel, L.A. A1 - de la Fuente, G.F. A1 - Navarro, R. A1 - Legall, Herbert A1 - Krüger, Jörg A1 - Bonse, Jörn T1 - Surface superconductivity changes of niobium sheets by femtosecond laser-induced periodic nanostructures N2 - Irradiation with ultra-short (femtosecond) laser beams enables the generation of sub-wavelength laser-induced periodic surface structures (LIPSS) over large areas with controlled spatial periodicity, orientation, and depths affecting only a material layer on the sub-micrometer scale. This study reports on how fs-laser irradiation of commercially available Nb foil samples affects their superconducting behavior. DC magnetization and AC susceptibility measurements at cryogenic temperatures and with magnetic fields of different amplitude and orientation are thus analyzed and reported. This study pays special attention to the surface superconducting layer that persists above the upper critical magnetic field strength Hc2, and disappears at a higher nucleation field strength Hc3. Characteristic changes were distinguished between the surface properties of the laser-irradiated samples, as compared to the corresponding reference samples (non-irradiated). Clear correlations have been observed between the surface nanostructures and the nucleation field Hc3, which depends on the relative orientation of the magnetic field and the surface patterns developed by the laser irradiation. KW - Niobium KW - Surface superconductivity KW - Laser-induced periodic surface structures (LIPSS) KW - Nanostructures PY - 2020 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-518462 DO - https://doi.org/10.3390/nano10122525 SN - 2079-4991 VL - 10(12) IS - Special issue "Laser-generated periodic nanostructures" SP - 1 EP - 16 PB - MDPI CY - Basel AN - OPUS4-51846 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Chan, George C.-Y. A1 - Hieftje, Gary M. A1 - Omenetto, Nicoló A1 - Axner, Ove A1 - Bengtson, Arne A1 - Bings, Nicolas H. A1 - Blades, Michael W. A1 - Bogaerts, Annemie A1 - Bolshov, Mikhail A. A1 - Broekaert, José A.C. A1 - Chan, WingTat A1 - Costa-Fernández, José M. A1 - Crouch, Stanley R. A1 - De Giacomo, Alessandro A1 - D’Ulivo, Alessandro A1 - Engelhard, Carsten A1 - Falk, Heinz A1 - Farnsworth, Paul B. A1 - Florek, Stefan A1 - Gamez, Gerardo A1 - Gornushkin, Igor B. A1 - Günther, Detlef A1 - Hahn, David W. A1 - Hang, Wei A1 - Hoffmann, Volker A1 - Jakubowski, Norbert A1 - Karanassios, Vassili A1 - Koppenaal, David W. A1 - Kenneth Marcus, R. A1 - Noll, Reinhard A1 - Olesik, John W. A1 - Palleschi, Vincenzo A1 - Panne, Ulrich A1 - Pisonero, Jorge A1 - Ray, Steven J. A1 - Resano, Martín A1 - Russo, Richard E. A1 - Scheeline, Alexander A1 - Smith, Benjamin W. A1 - Sturgeon, Ralph E. A1 - Todolí, José-Luis A1 - Tognoni, Elisabetta A1 - Vanhaecke, Frank A1 - Webb, Michael R. A1 - Winefordner, James D. A1 - Yang, Lu A1 - Yu, Jin A1 - Zhang, Zhanxia T1 - Landmark Publications in Analytical Atomic Spectrometry: Fundamentals and Instrumentation Development N2 - The almost-two-centuries history of spectrochemical analysis has generated a body of literature so vast that it has become nearly intractable for experts, much less for those wishing to enter the field. Authoritative, focused reviews help to address this problem but become so granular that the overall directions of the field are lost. This broader perspective can be provided partially by general overviews but then the thinking, experimental details, theoretical underpinnings and instrumental innovations of the original work must be sacrificed. In the present compilation, this dilemma is overcome by assembling the most impactful publications in the area of analytical atomic spectrometry. Each entry was proposed by at least one current expert in the field and supported by a narrative that justifies its inclusion. The entries were then assembled into a coherent sequence and returned to contributors for a round-robin review. KW - Analytical atomic spectrometry KW - Spectroscopy KW - Instrumental analysis PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-621588 DO - https://doi.org/10.1177/00037028241263567 SN - 1943-3530 VL - 78 SP - 1 EP - 456 PB - Sage CY - London AN - OPUS4-62158 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Pontes Rodrigues, A. C. A1 - Nunes Ribeiro, P. J. A1 - Österle, Werner A1 - de Farias Azevedo, C. R. T1 - Failure analysis as a tool to optimize the design of a ring on disc tribotest investigating the role of surface roughness N2 - The influence of the surface roughness of pearlitic grey cast iron discs on the formation of tribofilms and the evolution of the friction coefficient during a ring on disc tribotest with the addition of magnetite and magnetite–graphite nanopowders as interfacial media was investigated. The roughness parameters of the cast iron discs were varied by electro discharge machining (EDM) and grinding processes, producing four distinct surface roughness conditions. The evolution of the friction coefficient, however, did not reach the steady state for most of the samples and the role of the surface roughness on the friction coefficient could not be identified. Focused ion beam (FIB) microscopy on the cast iron discs was carried out to investigate the microstructure of the discs near the tribosurface. These results showed that the EDM process not only varied the surface roughness, but also changed the microstructure of the cast iron discs, promoting the incipient fusion of the cast iron surface, with the formation of ridges and casting defects (pores). As a result, a layer of rapidly solidified metal with a dendritic microstructure was formed near to the surface of the EDMed discs. KW - Ring-on disc tribotest KW - Surface roughness KW - EDM-processing KW - Rapid solification PY - 2015 DO - https://doi.org/10.1016/j.engfailanal.2015.03.011 SN - 1350-6307 SN - 1873-1961 VL - 56 SP - 131 EP - 141 PB - Elsevier Science Publ. CY - Oxford AN - OPUS4-34623 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bernicke, M. A1 - Ortel, Erik A1 - Reier, T. A1 - Bergmann, A. A1 - De Araujo, J.F. A1 - Strasser, P. A1 - Kraehnert, R. T1 - Iridium oxide coatings with templated porosity as highly active oxygen evolution catalysts: Structure-activity relationships N2 - Iridium oxide is the catalytic material with the highest stability in the oxygen evolution reaction (OER) performed under acidic conditions. However, its high cost and limited availability demand that IrO2 is utilized as efficiently as possible. We report the synthesis and OER performance of highly active mesoporous IrO2 catalysts with optimized surface area, intrinsic activity, and pore accessibility. Catalytic layers with controlled pore size were obtained by soft-templating with micelles formed from amphiphilic block copolymers poly(ethylene oxide)-b-poly(butadiene)-b-poly(ethylene oxide). A systematic study on the influence of the calcination temperature and film thickness on the morphology, phase composition, accessible surface area, and OER activity reveals that the catalytic performance is controlled by at least two independent factors, that is, accessible surface area and intrinsic activity per accessible site. Catalysts with lower crystallinity show higher intrinsic activity. The catalyst surface area increases linearly with film thickness. As a result of the templated mesopores, the pore surface remains fully active and accessible even for thick IrO2 films. Even the most active multilayer catalyst does not show signs of transport limitations at current densities as high as 75 mA cm-2. KW - Electrochemistry KW - Iridium KW - Structure–activity relationships KW - Template synthesis KW - Water splitting PY - 2015 DO - https://doi.org/10.1002/cssc.201402988 SN - 1864-5631 SN - 1864-564X VL - 8 IS - 11 SP - 1908 EP - 1915 PB - Wiley-VCH CY - Weinheim AN - OPUS4-33503 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Raysyan, Anna A1 - Eremin, S. A. A1 - Beloglazova, N. V. A1 - De Saeger, S. A1 - Gravel, I. V. T1 - Immunochemical approaches for detection of aflatoxin B1 in herbal medicines N2 - Introduction Aflatoxin B1 (AFB1) is a toxic low‐molecular‐weight secondary metabolite of Aspergillus flavus and A. parasiticus. AFB1 was classified as a Group I carcinogen by the World Health Organisation for Research on Cancer in 1993. AFB1 is an unavoidable natural contaminant of some herbal medicine, able to cause serious health issues for humans consuming the related medicine. Objective Therefore, this study aimed to develop an efficient fluorescence polarisation immunoassay (FPIA) and a rapid, low‐cost, and easy‐to‐use membrane‐based flow‐through immunoassay (MBA) for determination of AFB1 in herbal medicine Origanum vulgare L., Rubus idaeus L., Urtica dioica L. and Sorbus aucuparia L. Results A cut‐off level of the developed MBA was 0.8 ppb. Validation of the developed test was performed with blank and spiked samples. Using three naturally contaminated or three artificially spiked samples. The FPIA showed a linear working range of 8.6 to 64 ppb, and a half maximal inhibitory concentration (IC50) of 24 ppb. Conclusion The results were in good correlation with the enzymelinked immunosorbent assay (ELISA) results (the IC50 0.1 ppb). Both the sample preparation and analysis are simple, cost‐effective and easy to perform on‐site in non‐laboratory environments. Liquid chromatography with tandem mass spectrometry (LC‐MS/MS) was used as a confirmatory technique. KW - Fluorescence Polarisation Immunoassay KW - membrane-based flow-through immunoassay KW - Mycotoxins KW - Mykotoxine KW - Schnelltest PY - 2020 DO - https://doi.org/10.1002/pca.2931 SN - 1099-1565 VL - 31 IS - 5 SP - 662 EP - 669 PB - Wiley Online Libary CY - Hoboken, NJ, USA AN - OPUS4-51341 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rienitz, O. A1 - Jährling, R. A1 - Noordmann, J. A1 - Pape, C. A1 - Röhker, K. A1 - Vogl, Jochen A1 - Manzano, J. V. L. A1 - Kozlowski, W. A1 - Caciano de Siena, R. A1 - Marques Rodrigues, J. A1 - Galli, A. H. A1 - Yim, Y.-H. A1 - Lee, K.-S. A1 - Lee, J. H. A1 - Min, H.-S. A1 - Chingbo, C. A1 - Naijie, S. A1 - Qian, W. A1 - Ren, T. A1 - Jun, W. A1 - Tangpaisarnkul, N. A1 - Suzuki, T. A1 - Nonose, N. A1 - Mester, Z. A1 - Yang, L. A1 - Pagliano, E. A1 - Greenberg, P. A1 - Mariassy, M. A1 - Näykki, T. A1 - Cankur, O. A1 - Coskun, F. G. A1 - Ari, B. A1 - Can, S. Z. T1 - CCQM-K122 "Anionic impurities and lead in salt solutions" N2 - The determination of the mass fractions of bromide, sulfate, and lead as well as the isotopic composition of the lead (expressed as the molar mass and the amount fractions of all four stable lead isotopes) in an aqueous solution of sodium chloride with a mass fraction of 0.15 g/g was the subject of this comparison. Even though the mass fractions ranged from 3 μg/g (bromide) to 50 ng/g (lead), almost all results reported agreed with the according KCRVs. KW - Absolute isotope ratio KW - Lead isotope ratios KW - Metrology KW - Traceability PY - 2020 DO - https://doi.org/10.1088/0026-1394/57/1A/08012 VL - 57 IS - 1A SP - 8012 PB - IOP Science AN - OPUS4-51156 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schulze-Makuch, D. A1 - Lipus, D. A1 - Arens, F. L. A1 - Baque, M. A1 - Bornemann, T. L. V. A1 - de Vera, J. P. A1 - Flury, M. A1 - Froesler, J. A1 - Heinz, J. A1 - Hwang, Y. A1 - Kounaves, S. P. A1 - Mangelsdorf, K. A1 - Meckenstock, R. U. A1 - Pannekens, M. A1 - Probst, A. J. A1 - Saenz, J. S. A1 - Schirmack, J. A1 - Schloter, M. A1 - Schmitt-Kopplin, P. A1 - Schneider, Beate A1 - Uhl, J. A1 - Vestergaard, G. A1 - Valenzuela, B. A1 - Zamorano, P. A1 - Wagner, D. T1 - Microbial hotspots in lithic microhabitats inferred from DNA fractionation and metagenomics in the Atacama Desert N2 - The existence of microbial activity hotspots in temperate regions of Earth is driven by soil heterogeneities, especially the temporal and spatial availability of nutrients. Here we investigate whether microbial activity hotspots also exist in lithic microhabitats in one of the most arid regions of the world, the Atacama Desert in Chile. While previous studies evaluated the total DNA fraction to elucidate the microbial communities, we here for the first time use a DNA separation approach on lithic microhabitats, together with metagenomics and other analysis methods (i.e., ATP, PLFA, and metabolite analysis) to specifically gain insights on the living and potentially active microbial community. Our results show that hypolith colonized rocks are microbial hotspots in the desert environment. In contrast, our data do not support such a conclusion for gypsum crust and salt rock environments, because only limited microbial activity could be observed. The hypolith community is dominated by phototrophs, mostly Cyanobacteria and Chloroflexi, at both study sites. The gypsum crusts are dominated by methylotrophs and heterotrophic phototrophs, mostly Chloroflexi, and the salt rocks (halite nodules) by phototrophic and halotolerant endoliths, mostly Cyanobacteria and Archaea. The major environmental constraints in the organic-poor arid and hyperarid Atacama Desert are water availability and UV irradiation, allowing phototrophs and other extremophiles to play a key role in desert ecology. KW - Desert ecology KW - Extremophile KW - Hyperarid PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-527959 DO - https://doi.org/10.3390/microorganisms9051038 SN - 2076-2607 VL - 9 IS - 5 SP - 1038 PB - MDPI CY - Basel AN - OPUS4-52795 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jablonka, Kevin Maik A1 - Ai, Qianxiang A1 - Al-Feghali, Alexander A1 - Badhwar, Shruti A1 - Bocarsly, Joshua D. A1 - Bran, Andres M. A1 - Bringuier, Stefan A1 - Brinson, L. Catherine A1 - Choudhary, Kamal A1 - Circi, Defne A1 - Cox, Sam A1 - de Jong, Wibe A. A1 - Evans, Matthew L. A1 - Gastellu, Nicolas A1 - Genzling, Jerome A1 - Gil, María Victoria A1 - Gupta, Ankur K. A1 - Hong, Zhi A1 - Imran, Alishba A1 - Kruschwitz, Sabine A1 - Labarre, Anne A1 - Lála, Jakub A1 - Liu, Tao A1 - Ma, Steven A1 - Majumdar, Sauradeep A1 - Merz, Garrett W. A1 - Moitessier, Nicolas A1 - Moubarak, Elias A1 - Mouriño, Beatriz A1 - Pelkie, Brenden A1 - Pieler, Michael A1 - Ramos, Mayk Caldas A1 - Ranković, Bojana A1 - Rodriques, Samuel G. A1 - Sanders, Jacob N. A1 - Schwaller, Philippe A1 - Schwarting, Marcus A1 - Shi, Jiale A1 - Smit, Berend A1 - Smith, Ben E. A1 - Van Herck, Joren A1 - Völker, Christoph A1 - Ward, Logan A1 - Warren, Sean A1 - Weiser, Benjamin A1 - Zhang, Sylvester A1 - Zhang, Xiaoqi A1 - Zia, Ghezal Ahmad Jan A1 - Scourtas, Aristana A1 - Schmidt, K. J. A1 - Foster, Ian A1 - White, Andrew D. A1 - Blaiszik, Ben T1 - 14 examples of how LLMs can transform materials science and chemistry: a reflection on a large language model hackathon N2 - Large-language models (LLMs) such as GPT-4 caught the interest of many scientists. Recent studies suggested that these models could be useful in chemistry and materials science. To explore these possibilities, we organized a hackathon. This article chronicles the projects built as part of this hackathon. Participants employed LLMs for various applications, including predicting properties of molecules and materials, designing novel interfaces for tools, extracting knowledge from unstructured data, and developing new educational applications. The diverse topics and the fact that working prototypes could be generated in less than two days highlight that LLMs will profoundly impact the future of our fields. The rich collection of ideas and projects also indicates that the applications of LLMs are not limited to materials science and chemistry but offer potential benefits to a wide range of scientific disciplines. KW - Large Language model KW - Hackathon KW - Concrete KW - Prediction KW - Inverse Design KW - Orchestration PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-589961 DO - https://doi.org/10.1039/d3dd00113j VL - 2 IS - 5 SP - 1233 EP - 1250 PB - Royal Society of Chemistry (RSC) AN - OPUS4-58996 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Galleani, Gustavo A1 - Lodi, Thiago A. A1 - Conner, Robin L. A1 - Jacobsohn, Luiz G. A1 - de Camargo, Andrea Simone Stucchi T1 - Photoluminescence and X-ray induced scintillation in Gd3+-Tb3+ co-doped fluoride-phosphate glasses, and derived glass-ceramics containing NaGdF4 nanocrystals N2 - The glass system (50NaPO3–20BaF2–10CaF2–20GdF3)-xTbCl3 with x = 0.3, 1, 3, 5, and 10 wt % was investigated. We successfully produced transparent glass ceramic (GC) scintillators with x = 1 through a melt-quenching process followed by thermal treatment. The luminescence and crystallization characteristics of these materials were thoroughly examined using various analytical methods. The nanocrystallization of Tb3+-doped Na5Gd9F32 within the doped fluoride-phosphate glasses resulted in enhanced photoluminescence (PL) and radioluminescence (RL) of the Tb3+ ions. The GC exhibited an internal PL quantum yield of 33 % and the integrated RL intensity across the UV-visible range was 36 % of that reported for the commercial BGO powder scintillator. This research showcases that Tb-doped fluoridephosphate GCs containing nanocrystalline Na5Gd9F32 have the potential to serve as efficient scintillators while having lower melting temperature compared to traditional silicate and germanate glasses. KW - Glass scintillator KW - Fluoride phosphate glasses KW - Gd3+ KW - Tb3+ PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-603588 DO - https://doi.org/10.1016/j.omx.2023.100288 VL - 21 SP - 1 EP - 9 PB - Elsevier B.V. AN - OPUS4-60358 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Habig, Karl-Heinz A1 - Broszeit, E. A1 - de Gee, A. W. J. T1 - friction and wear tests on metallic bearing materials for oil-lubricated bearings PY - 1981 SN - 0043-1648 VL - 69 SP - 43 EP - 54 PB - Elsevier CY - Amsterdam AN - OPUS4-32270 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Westwood, S. A1 - Josephs, R. A1 - Daireaux, A. A1 - Wielgosz, R. A1 - Davies, S. A1 - Kang, M. A1 - Ting, H. A1 - Philipp, Rosemarie A1 - Malz, Frank A1 - Shimizu, Y. A1 - Frias, E. A1 - Pérez, M. A1 - Apps, P. A1 - Fernandes-Whaley, M. A1 - De Vos, B. A1 - Wiagnon, K. A1 - Ruangrittinon, N. A1 - Wood, S. A1 - Duewer, D.L. A1 - Schantz, M.M. A1 - Bedner, M. A1 - Hancock, D. A1 - Esker, J. T1 - An international comparison of mass fraction purity assignment of theophylline: CCQM pilot study CCQM-P20.e (Theophylline) PY - 2009 DO - https://doi.org/10.1088/0026-1394/46/1A/08019 SN - 0026-1394 SN - 1681-7575 VL - 46 IS - 08019 SP - 1 EP - 37 PB - Inst. of Physics Publ. CY - Bristol AN - OPUS4-20030 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Narbonneau, F. A1 - De Jonckheere, J. A1 - Jeanne, M. A1 - Kinet, D. A1 - Witt, Jens A1 - Krebber, Katerina A1 - Paquet, B. A1 - Depré, A. A1 - D´Angelo, L.T. A1 - Thiel, T. A1 - Logier, R. ED - Popp, J. T1 - OFSETH: Optical technologies embedded in smart medical textile for continuous monitoring of respiratory motions under magnetic resonance imaging N2 - The potential impact of optical fiber sensors embedded into medical textiles for the continuous monitoring of the patient during Magnetic Resonance Imaging (MRI) is now proved. We report how two pure optical technologies can successfully sense textile elongation between, 0% and 3%, while maintaining the stretching properties of the textile substrates for a good comfort of the patient. Investigating influence of different patients' morphology as well as textile integration issues to let free all vitals organs for medical staff actions, the OFSETH harness allows a continuous measurement of respiration movements. For example, anaesthesia for MRI examination uses the same drugs as for any surgical procedure. Even if spontaneous respiration can be preserved most of the time, spontaneous respiration is constantly at risk of being impaired by anaesthetic drugs or by upper airway obstruction. Monitoring of the breathing activity is needed to assess adequate ventilation or to detect specific obstruction patterns. Moreover artefacts due to physiological motions induce a blooming effect on the MRI result. The use of synchronisation devices allows reducing these effects. Positioned at certain strategic places according to the investigated organ, the presented sensors could constitute an efficient and adapted solution for respiratory synchronisation of the MRI acquisition. KW - MRI KW - Smart textile KW - Healthcare monitoring KW - Optical sensor KW - FBG KW - Respiratory sensor PY - 2010 SN - 9780819481887 DO - https://doi.org/10.1117/12.854386 VL - 7715 SP - 77151D-1 - 77151D-12 AN - OPUS4-22839 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ridsdale, P. A1 - Cali, J. A1 - Cox, J. A1 - de Bievre, P. A1 - van der Eijk, W. A1 - Marshal, A. A1 - Wandelburg, Klaus T1 - Panel on General Principles of the Certification Procedure for RM's T2 - International Symposium on the Production and Use of Reference Materials CY - Berlin, BAM DA - 1979-11-13 PY - 1980 SP - 443 EP - 459 PB - BAM CY - Berlin AN - OPUS4-9273 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - De Araújo, A. A1 - Panossian, Z. A1 - Portella, Pedro Dolabella A1 - Bäßler, Ralph T1 - Monitoramento da corrosao em estruturas de concreto: sensor galvânico N2 - O monitoramento das estruturas de concreto possibilita que o risco de corrosão seja estimado ao longo dos anos de sua utilização. Com o conhecimento desse risco, intervenções de prevenção da corrosão ou de controle da corrosão já estabelecida podem ser programadas e realizadas em períodos adequados. Na prática, o risco de corrosão é avaliado por meio da verificação periódica do estado da armadura e das alterações nas propriedades do concreto. Isso pode ser feito por meio do embutimento no concreto de cobrimento de sensores de aquisição contínua de dados. Há diferentes tipos de sensores de aquisição contínua de dados. Um dos mais conhecidos é o sensor galvânico que consta de um conjunto de barras de aço-carbono, eletricamente isoladas. Com o embutimento do sensor, essas barras ficam posicionadas em diferentes e conhecidas profundidades do concreto de cobrimento da armadura. O risco de corrosão da armadura é monitorado com a periódica medição da corrente galvânica em cada uma das barras do sensor. Essa medição, dentre outras informações do sensor galvânico foram abordadas em artigo anterior. Além do sensor galvânico, destacam-se o sensor de umidade e o de taxa de corrosão, que monitoram parâmetros importantes relacionados ao estabelecimento e evolução de processo corrosivo das armaduras. A seguir esses sensores são apresentados, bem como o sensor de fibra óptica, o qual apresenta algumas vantagens em relação aos demais mencionados, embora ainda seja de uso restrito. KW - Sensor da corrosao PY - 2013 SN - 0104-1053 VL - 194 IS - Maio SP - 62 EP - 66 PB - PINI AN - OPUS4-29403 LA - por AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kelm, Jürgen A1 - Kühn, H. A1 - Klein, M. A1 - Wiesmath, A. A1 - Demco, D.E. A1 - Blümich, B. A1 - Gold, P.W. T1 - The NMR-MOUSE: quality control of elastomers KW - NMR-MOUSE KW - Double-quantum NMR KW - Quality control KW - Elastomers PY - 2001 SN - 1090-7807 SN - 0022-2364 VL - 19 SP - 497 EP - 499 PB - Elsevier CY - San Diego, Calif. AN - OPUS4-1034 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reuter, T. A1 - Borges de Oliveira, F. A1 - Abt, Ch. A1 - Ballach, F. A1 - Bartscher, M. A1 - Bellon, Carsten A1 - Dennerlein, F. A1 - Fuchs, P. A1 - Günnewig, O. A1 - Hausotte, T. A1 - Hess, J. A1 - Kasperl, S. A1 - Maass, N. A1 - Kimmig, W. A1 - Schielein, R. A1 - von Schmid, M. A1 - Suppes, A. A1 - Wagner, G. A1 - Watzl, Ch. A1 - Wohlgemuth, F. T1 - Introduction to “Realistic Simulation of real CT systems with a basic-qualified Simulation Software - CTSimU2“ N2 - The lack of traceability to meter of X-ray Computed Tomography (CT) measurements still hinders a more extensive acceptance of CT in coordinate metrology and industry. To ensure traceable, reliable, and accurate measurements, the determination of the task-specific measurement uncertainty is necessary. The German guideline VDI/VDE 2630 part 2.1 describes a procedure to determine the measurement uncertainty for CT experimentally by conducting several repeated measurements with a calibrated test specimen. However, this experimental procedure is cost and effort intensive. Therefore, the simulation of dimensional measurement tasks conducted with X-ray computed tomography can close these drawbacks. Additionally, recent developments towards a resource and cost-efficient production (“smart factory”) motivate the need for a corresponding numerical model of a CT system (“digital twin”) as well. As there is no standardized procedure to determine the measurement uncertainty of a CT system by simulation at the moment, the project series CTSimU was initiated, aiming at this gap. Concretely, the goal is the development of a procedure to determine the measurement uncertainty numerically by radiographic simulation. The first project (2019-2022), "Radiographic Computed Tomography Simulation for Measurement Uncertainty Evaluation - CTSimU" developed a framework to qualify a radiographic simulation software concerning the correct simulation of physical laws and functionalities. The most important outcome was a draft for a new guideline VDI/VDE 2630 part 2.2, which is currently under discussion in the VDI/VDE committee. The follow-up project CTSimU2 "Realistic Simulation of real CT systems with a basic-qualified Simulation Software" will deal with building and characterizing a digital replica of a specific real-world CT system. The two main targets of this project will be a toolbox including methods and procedures to configure a realistic CT system simulation and to develop tests to check if this replica is sufficient enough. The result will be a draft for a follow-up VDI/VDE guideline proposing standardized procedures to determine a CT system's corresponding characteristics and test the simulation (copy) of a real-world CT system which we call a "digital twin". T2 - 12th Conference on Industrial Computed Tomography (iCT) 2023 CY - Fürth, Germany DA - 27.02.2023 KW - dXCT KW - X-ray computed tomography KW - Simulation PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-589204 DO - https://doi.org/10.58286/27715 VL - 28 IS - 3 SP - 1 EP - 5 PB - NDT.net AN - OPUS4-58920 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Szymoniak, Paulina A1 - Kolmangadi, Mohamed A. A1 - Böhning, Martin A1 - De Souza, N. R. A1 - Juranyi, F. A1 - Zorn, R. A1 - Schönhals, Andreas T1 - Inelastic and Quasielastic Neutron Scattering on Polynorbornenes with Bulky Carbocyclic Side groups N2 - This study investigates the molecular mobility and vibrational properties of polynorbornenes with bulky carbocyclic side groups using inelastic and quasielastic neutron scattering techniques. The polymers, synthesized via metathesis and addition polymerization, exhibit varying degrees of microporosity, which ignificantly influences their gas separation performance. By inelastic neutron scattering experiments, it could be shown that all considered polymers have excess contributions to the low frequency vibrational density of states known as the Boson peak. The maximum frequency of the Boson peak correlates to the microporosity of the polymers. This correlation supports the sound wave interpretation of the Boson peak, suggesting that the microporous structure enhances the compressibility of the material at a microscopic length scale. The molecular mobility, particularly the methyl group rotation, was characterized using elastic scans and quasielastic neutron scattering. The study revealed a temperature dependent relaxation process, with the onset of molecular fluctuations observed around 200 K for the polymer containing methyl groups. For the polymer having no methyl groups only elastic scattering is observed. The methyl group rotation was analyzed in terms of a jump diffusion in a threefold potential with three equivalent energy minima. This leads to an almost correct description of the q dependence of the elastic incoherent scattering function when the number of hydrogen nuclei undergoing the methyl group rotation is considered. It was further evidenced that the fraction of methyl undergoing the methyl group rotation increases with increasing temperature. KW - Polymers of Intrinsic Microporosity KW - Neutron scattering PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-630297 DO - https://doi.org/10.1016/j.polymer.2025.128358 SN - 1873-2291 VL - 328 SP - 241 PB - Elsevier Ltd. AN - OPUS4-63029 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - de Krom, I. A1 - Heikens, D. A1 - Horn, Wolfgang A1 - Wilke, Olaf A1 - Richter, Matthias A1 - Baldan, A. T1 - Metrological generation of SI-traceable gas-phase standards and reference materials for (semi-) volatile organic compounds N2 - EN 16516 sets specifications for the determination of emissions into indoor air from construction products. Reliable, accurate and International System of Unit (SI)-traceable measurement results of the emissions are the key to consumer protection. Such measurement results can be obtained by using metrologically traceable reference materials. Gas-phase standards of volatile organic compounds (VOCs) in air can be prepared by a variety of dynamic methods according to the ISO 6145 series. However, these methods are not always applicable for semi-VOCs (SVOCs) due to their high boiling point and low vapour pressure. Therefore, a novel dynamic gas mixture generation system has been developed. With this system gas-phase standards with trace level VOCs and SVOCs in air can be prepared between 10 nmol mol−1 and 1000 nmol mol−1. The VOCs and SVOCs in this study have normal boiling points ranging from 146 °C to 343 °C. Metrologically traceable reference materials of the gas-phase standard were obtained by sampling of the VOC gas-phase standard into Tenax TA® sorbent material in SilcoNert® coated stainless steel tubes. Accurately known masses between 10 ng and 1000 ng per VOC were sampled. These reference materials were used to validate the dynamic system. Furthermore, the storage and stability periods of the VOCs in the reference materials were determined as these are crucial characteristics to obtain accurate and SI-traceable reference materials. In a round robin test (RRT), the reference materials were used with the aim of demonstrating the feasibility of providing SI-traceable standard reference values for SVOCs for interlaboratory comparison purposes. Based on the results from the validation, the storage and stability studies and the RRT, gas-phase standards and reference materials of VOCs and SVOCs with relative expanded uncertainties between 5% and 12% (k = 2) have been developed. These reference standards can be used as calibrants, reference materials or quality control materials for the analysis of VOC emissions. KW - SVOC KW - Dynamic calibration gas mixtures KW - Reference materials KW - Indoor air KW - Thermal desorption PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-565978 DO - https://doi.org/10.1088/1361-6501/aca704 VL - 34 IS - 3 SP - 1 EP - 13 PB - IOP Publishing AN - OPUS4-56597 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Witt, Jens A1 - Narbonneau, F. A1 - Schukar, Marcus A1 - Krebber, Katerina A1 - De Jonckheere, J. A1 - Jeanne, M. A1 - Kinet, D. A1 - Paquet, B. A1 - Depré, A. A1 - D´Angelo, L.T. A1 - Thiel, T. A1 - Logier, R. T1 - Medical textiles with embedded fiber optic sensors for monitoring of respiratory movement N2 - For patients under Magnetic Resonance Imaging (MRI) spontaneous respiration is constantly at risk of being impaired by anesthetic drugs or by upper airway obstruction. Therefore, continuous monitoring of the breathing activity is needed to assess adequate ventilation or to detect specific obstruction patterns. The paper describes three MRI compatible respiration sensors based on pure optical technologies developed within the EU FP6 project OFSETH. The sensors are based on fiber Bragg gratings, optical time-domain reflectometry and macrobending effects. The developed smart medical textiles can sense elongation up to 3% while maintaining the stretching properties of the textile substrates for patient's comfort. The OFSETH harness allows a continuous measurement of abdominal and thoracic respiration movement while all vitals organs are free for medical staff actions. The sensors were tested in MRI environment and on healthy adults. KW - Fiber optic sensor KW - Polymer optical fiber (POF) sensor KW - Respiratory sensor KW - Smart medical textile KW - MRI KW - Smart textile KW - Healthcare monitoring KW - Optical sensor KW - FBG PY - 2012 DO - https://doi.org/10.1109/JSEN.2011.2158416 SN - 1530-437X SN - 1558-1748 VL - 12 IS - 1 SP - 246 EP - 254 CY - New York, NY, USA AN - OPUS4-25649 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Khan, K. A1 - Mohr, Gunther A1 - Hilgenberg, Kai A1 - De, A. T1 - Probing a novel heat source model and adaptive remeshing technique to simulate laser powder bed fusion with experimental validation N2 - A finite element method based three-dimensional heat transfer model with adaptive remeshing is presented to simulate the building of multiple tracks and layers in laser powder bed fusion of metallic powders with enhanced computational competence. A dimensional analysis is undertaken to define the heat source dimensions as function of laser parameters and properties of alloy powder. The computational model is used to calculate the melt pool cross sections for multiple combinations of laser power and scanning velocities considering multi-track-multi-layer builds of SS316L powder. The computed results are verified extensively with the corresponding experimentally measured ones. The model is utilized further to examine its ability to predict defects such as melt track discontinuity and incomplete fusion between neighboring tracks and layers. Overall, the adaptive remeshing and the proposed heat source expression could significantly enhance the model competence by reducing the computational time and memory while maintaining the accuracy of results in simulating laser powder bed fusion of multiple tracks and layers. KW - Selective laser melting (SLM) KW - Laser powder bed fusion (L-PBF) KW - Adaptive remeshing KW - SS316L alloy KW - Pool dimensions KW - Melt pool defects PY - 2020 DO - https://doi.org/10.1016/j.commatsci.2020.109752 VL - 181 SP - 109752 PB - Elsevier B. CY - Amsterdam AN - OPUS4-50703 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Witt, Jens A1 - Schukar, Marcus A1 - Krebber, Katerina A1 - Jonckheere, J. de A1 - Paquet, B. A1 - Depré, A. T1 - Respiratory sensor based on POF OTDR N2 - We report on the characterization and test of a respiratory sensor based on POF OTDR, developed for monitoring of patients during MRI examination. The sensor is based on an optical fibre integrated into an elastic belt using a macrobending layout. T2 - POF 2009 - 18th International conference on plastic optical fibers CY - Sydney, Australia DA - 2009-09-07 KW - Faseroptischer Sensor KW - Medizinische Textilien KW - Intelligente Textilien KW - Atmungssensor KW - OTDR KW - POF PY - 2009 IS - Session 6 ( S6_74) SP - 1 EP - 4 CY - Sydney, Australia AN - OPUS4-19889 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Witt, Jens A1 - Narbonneau, F. A1 - Schukar, Marcus A1 - Krebber, Katerina A1 - De Jonckheere, J. A1 - Jeanne, M. A1 - Kinet, D. A1 - Paquet, B. A1 - Depré, A. A1 - D´Angelo, L.T. A1 - Thiel, T. A1 - Logier, R. ED - Santos, J.L. ED - Culshaw, B. ED - López-Higuera, J.M. ED - MacPherson, W.N. T1 - Smart medical textiles with embedded optical fibre sensors for continuous monitoring of respiratory movements during MRI N2 - We report on three respiration sensors based on pure optical technologies developed during the FP6 EU project OFSETH. The developed smart medical textiles can sense elongation up to 3%, while maintaining the stretching properties of the textile substrates for a good comfort of the patient. The sensors, based on silica and polymer fibre, are developed for monitoring of patients during MRI examination. The OFSETH harness allows a continuous measurement of respiration movements while all vitals organs are free for medical staff actions. The sensors were tested in MRI environment and on healthy adults. T2 - 4th European workshop on optical fibre sensors CY - Porto, Portugal DA - 2010-09-08 KW - Respiratory sensor KW - Fibre optic sensor KW - Optical time-domain reflectometry (OTDR) KW - MRI KW - Smart textile KW - Healthcare monitoring KW - Fibre Bragg grating (FBG) PY - 2010 SN - 978-0-8194-8083-5 SN - 0277-786X N1 - Serientitel: Proceedings of SPIE – Series title: Proceedings of SPIE IS - 7653 SP - Paper 115, 76533B-1 - 76533B-4 PB - SPIE, the International Society for Optical Engineering CY - Bellingham, Wash. AN - OPUS4-22552 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Billimoria, K. A1 - Diaz Fernandez, Y. A. A1 - Andresen, Elina A1 - Sorzabal-Bellido, I. A1 - Huelga-Suarez, G. A1 - Bartczak, D. A1 - Ortiz de Solórzano, C. A1 - Resch-Genger, Ute A1 - Goenaga Infante, H. T1 - The potential of bioprinting for preparation of nanoparticle-based calibration standards for LA-ICP-ToF-MS quantitative imaging N2 - This paper discusses the feasibility of a novel strategy based on the combination of bioprinting nano-doping technology and laser ablation-inductively coupled plasma time-of-flight mass spectrometry analysis for the preparation and characterization of gelatin- based multi-element calibration standards suitable for quantitative imaging. To achieve this, lanthanide up-conversion nanoparticles were added to a gelatin matrix to produce the bioprinted calibration standards. The features of this bioprinting approach were com- pared with manual cryosectioning standard preparation, in terms of throughput, between batch repeatability and elemental signal homogeneity at 5 μm spatial resolution. By using bioprinting, the between batch variability for three independent standards of the same concentration of 89 Y (range 0–600 mg/kg) was reduced to 5% compared to up to 27% for cryosectioning. On this basis, the relative standard deviation ( RSD ) obtained between three independent calibration slopes measured within 1 day also reduced from 16% (using cryosectioning ) to 5% (using bioprinting), supporting the use of a single standard preparation replicate for each of the concentrations to achieve good calibration performance using bioprinting. This helped reduce the analysis time by approximately 3-fold. With cryosectioning each standard was prepared and sectioned individually, whereas using bio-printing it was possible to have up to six different standards printed simultaneously, reducing the preparation time from approximately 2 h to under 20 min (by approxi- mately 6-fold). The bio-printed calibration standards were found stable for a period of 2 months when stored at ambient temperature and in the dark. KW - Environmental analysis KW - LA-ICP-MS KW - Lanthanide KW - Tag KW - Fluorescence KW - Nanoparticles KW - Reference material KW - Quality assurance KW - 3D-printing KW - Synthesis KW - Production KW - Multimodal PY - 2022 DO - https://doi.org/10.1093/mtomcs/mfac088 SN - 1756-591X VL - 14 IS - 12 SP - 1 EP - 9 PB - Oxford University Press CY - Oxford AN - OPUS4-57018 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Sänger, Johanna A1 - König, N.F. A1 - De Marzi, A. A1 - Zocca, Andrea A1 - Franchin, G. A1 - Bermejo, R. A1 - Colombo, P. A1 - Günster, Jens T1 - Linear volumetric additive manufacturing of zirconia from a transparent photopolymerizable ceramic slurry via Xolography N2 - Advanced ceramics printed with photon-based additive manufacturing deals with anisotropic mechanical properties from the layer-by-layer manufacturing. Motivated by the success in using highly filled transparent slurries containing nanoparticles for powder-based two-photon-polymerization (2PP) for advanced ceramic printing, this works approach is the transfer to Xolography, a volumetric additive manufacturing technology based on linear two-photon excitation and without recoating steps. This paper reports the results of a preliminary investigation optimizing the photocurable slurry to the requirements of Xolography in terms of transparency, over a significantly larger mean free path, compared to 2PP. A feedstock filled with 70 % weight fraction of ceramic particles (∼30 vol%) exhibiting an exceptionally high degree of transparency in the relevant wavelength range of 400–800 nm was prepared from 5 nm zirconia nanoparticles. The high transparency of the photocurable slurry is attributed to the near-monomodal particle size distribution of the zirconia nanoparticles used. KW - Additive manufacturing KW - Xolography KW - Ceramic PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-608908 DO - https://doi.org/10.1016/j.oceram.2024.100655 SN - 2666-5395 VL - 19 SP - 1 EP - 9 PB - Elsevier BV AN - OPUS4-60890 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Brusamarello-Santos, L. C. C. A1 - Alberton, D. A1 - Valdameri, G. A1 - Camilios-Neto, D. A1 - Covre, R. A1 - Lopes, K. d. P. A1 - Zibetti Tadra-Sfeir, M. A1 - Faoro, H. A1 - Adele Monteiro, R. A1 - Barbosa-Silva, A. A1 - Broughton, William John A1 - Oliveira Pedrosa, F. A1 - Wassem, R. A1 - de Souza, E.M. T1 - Modulation of defence and iron homeostasis genes in rice roots by the diazotrophic endophyte Herbaspirillum seropedicae N2 - Rice is staple food of nearly half the world’s population. Rice yields must therefore increase to feed ever larger populations. By colonising rice and other plants, Herbaspirillum spp. stimulate plant growthand productivity. However the molecular factors involved are largely unknown. To further explore this interaction, the transcription profiles of Nipponbare rice roots inoculated with Herbaspirillum seropedicae were determined by RNA-seq. Mapping the 104 million reads against the Oryza sativa cv. Nipponbare genome produced 65 million unique mapped reads that represented 13,840 transcripts each with at least two-times coverage. About 7.4% (1,014) genes were differentially regulated and of these 255 changed expression levels more than two times. Several of the repressed genes encoded proteins related to plant defence (e.g. a putative probenazole inducible protein), plant disease resistance as well as enzymes involved in flavonoid and isoprenoid synthesis. Genes related to the synthesis and efflux of phytosiderophores (PS) and transport of PS-iron complexes were induced by the bacteria. These data suggest that the bacterium represses the rice defence system while concomitantly activating iron uptake. Transcripts of H. seropedicae were also detected amongst which transcripts of genes involved in nitrogen fixation, cell motility and cell wall synthesis were the most expressed. KW - Herbaspirillum seropedicae KW - Pathogen KW - Rice KW - qPCR KW - Genome PY - 2019 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-490122 DO - https://doi.org/10.1038/s41598-019-45866-w SN - 2045-2322 VL - 9 SP - 10573-1 EP - 10573-15 PB - Nature CY - London AN - OPUS4-49012 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nai, Corrado A1 - Wong, Helen A1 - Pannenbecker, A. A1 - Broughton, William J. A1 - Benoit, I. A1 - De Vries, R.P. A1 - Gueidan, C. A1 - Gorbushina, Anna T1 - Nutritional physiology of a rock-inhabiting, model microcolonial fungus from an ancestral lineage of the chaetothyriales (ascomycetes) N2 - Rock-inhabiting black fungi [also microcolonial or meristematic fungi (MCF)] are a phylogenetically diverse group of melanised ascomycetes with distinctive morphological features that confer extensive stress tolerance and permit survival in hostile environments. The MCF strain A95 Knufia petricola (syn. Sarcinomyces petricola) belongs to an ancestral lineage of the order Chaetothyriales (class Eurotiomycetes). K. petricola strain A95 is a rock-inhabiting MCF and its growth requirements were studied using the 96-well plate-based Biolog™ System under ~1070 different conditions (osmotic stress, pH growth optima, growth factor requirements and nutrient catabolism). A95 is an osmotolerant, oligotrophic MCF that grows best around pH 5. Remarkably, A95 shows metabolic activity in the absence of added nitrogen, phosphorus or sulphur. Correlations could be drawn between the known nutrient requirements of A95 and what probably is available in sub-aerial systems (rock and other material surfaces). Detailed knowledge of A95's metabolic requirements allowed formulation of a synthetic medium that supports strong fungal growth. KW - Knufia petricola (syn. Sarcinomyces petricola) KW - A95 KW - Chaetothyriales (Eurotiomycetes) KW - Microcolonial fungi KW - Melanised rock-inhabiting fungi KW - Biolog™ system KW - Physiological characterisation PY - 2013 DO - https://doi.org/10.1016/j.fgb.2013.04.001 SN - 1087-1845 SN - 0147-5975 SN - 1096-0937 VL - 56 SP - 54 EP - 66 PB - Elsevier CY - Amsterdam [u.a.] AN - OPUS4-28865 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - de Carvello, J. M. F. A1 - Schmidt, Wolfram A1 - Kühne, Hans-Carsten A1 - Fiorotti Peixoto, R. A. T1 - Influence of high-charge and low-charge PCE-based superplasticizers on Portland cement pastes containing particle-size designed recycled mineral admixtures N2 - Design : and use of engineered recycled mineral admixtures obtained from industrial and mineral waste are promising strategies to increase the range of materials suitable for use in cement-based composites. In this work, Portland cement-blended pastes containing mineral admixtures designed for improving particle packing were evaluated in the presence of low- and high-charge polycarboxylate-based superplasticizers. The powders were obtained from basic oxygen furnace slag, iron ore tailings, quartz mining tailings, and quartzite mining tailings. The zeta-potentials of the particles were obtained via electrophoretic mobility. The flow properties were evaluated by rheological tests performed in a Couette type rheometer. The hydration kinetics was evaluated by isothermal calorimetry and an adapted method based on the Vicat needle test. The high-charge PCE and the finer mineral admixtures produced more stable blends. Coarser mineral admixtures led to increased flowability and delayed hydration compared to finer ones. Steel slag powders presented the most significant plasticizer effects, but also the largest setting delays and segregation tendency. Quartz-rich superfines reduced the setting delays caused by the superplasticizers. In summary, both superplasticizers were effective in improving flow properties, but the high-charge PCE was effective in preventing segregation in pastes containing mineral admixtures coarser and heavier than cement. KW - Engineered recycled mineral admixtures KW - Rheology KW - PCE-Based superplasticizer KW - Steel slag KW - Mining tailing PY - 2020 DO - https://doi.org/10.1016/j.jobe.2020.101515 VL - 32 SP - 1 EP - 16 PB - Elsevier AN - OPUS4-58395 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Franco de Carvalho, J. M. A1 - Defàveri, K- A1 - Castro Mendes, J. A1 - Schmidt, Wolfram A1 - Kühne, Hans-Carsten A1 - Fiorotti Peixoto, R. A. T1 - Influence of particle size-designed recycled mineral admixtures on the properties of cement-based composites N2 - In this work, engineered recycled mineral admixtures were obtained from four different industrial residues: basic oxygen furnace slag, iron ore tailings, quartz mining tailings and quartzite mining tailings. The grinding performance was evaluated in two different programs and the characterization included chemical and mineralogical composition, particle morphology, and physical properties. Performance evaluations were carried out in blended pastes and mortars, including flow properties, hydration kinetics, soundness, pozzolanic activity, and compressive strength. Coarser-than-cement admixtures allowed better flow performance, greater dimensional stability and more economical production, while finer-thancementn admixtures improved mechanical performance by both filler effect and cementing activity. KW - Engineered recycled mineral admixtures KW - Rheology KW - Hydration kinetics KW - Basic oxygen furnace slag KW - Iron ore tailings KW - Mining tailings PY - 2021 DO - https://doi.org/10.1016/j.conbuildmat.2020.121640 SN - 0950-0618 VL - 272 SP - 1 EP - 13 PB - Elsevier Ltd. AN - OPUS4-58255 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bugel, S. A1 - Hahnel, M. A1 - Kunde, T. A1 - de Sousa Amadeu, Nader A1 - Sun, Y. A1 - Spieß, A. A1 - Beglau, T. H. Y. A1 - Janiak, C. A1 - Schmidt, B. M. T1 - Synthesis and Characterization of a Crystalline Imine-Based Covalent Organic Framework with Triazine Node and Biphenyl Linker and Its Fluorinated Derivate for CO2/CH4 Separation N2 - A catalyst-free Schiff base reaction was applied to synthesize two imine-linked covalent organic frameworks (COFs). The condensation reaction of 1,3,5-tris-(4-aminophenyl)triazine (TAPT) with 4,4′-biphenyldicarboxaldehyde led to the structure of HHU-COF-1 (HHU = Heinrich-Heine University). The fluorinated analog HHU-COF-2 was obtained with 2,2′,3,3′,5,5′,6,6′-octafluoro-4,4′-biphenyldicarboxaldehyde. Solid-state NMR, infrared spectroscopy, X-ray photoelectron spectroscopy, and elemental analysis confirmed the successful formation of the two network structures. The crystalline materials are characterized by high Brunauer–Emmett–Teller surface areas of 2352 m2/g for HHU-COF-1 and 1356 m2/g for HHU-COF-2. The products of a larger-scale synthesis were applied to prepare mixed-matrix membranes (MMMs) with the polymer Matrimid. CO2/CH4 permeation tests revealed a moderate increase in CO2 permeability at constant selectivity for HHU-COF-1 as a dispersed phase, whereas application of the fluorinated COF led to a CO2/CH4 selectivity increase from 42 for the pure Matrimid membrane to 51 for 8 wt% of HHU-COF-2 and a permeability increase from 6.8 to 13.0 Barrer for the 24 wt% MMM. KW - MOF KW - Filter PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-547632 DO - https://doi.org/10.3390/ma15082807 SN - 1996-1944 VL - 15 IS - 8 SP - 1 EP - 18 PB - MDPI AN - OPUS4-54763 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Trappe, Volker A1 - Spancken, D. A1 - Zeiser, A. A1 - Kose, K. A1 - DeMonte, M. T1 - Kurzfaserverstärkte Thermoplaste - Zug-Druck-Schubprüfung mit einem Rohrprobekörper unter schwingender Beanspruchung N2 - Diese DIN SPEC legt ein Verfahren für die Prüfung von unverstärkten und partikel- und kurzfaserverstärkten Kunststoffen mittels Zug-Druck-Schubprüfung fest. Dieses Verfahren findet Anwendung zur Bestimmung der Schwingfestigkeit im Bereich von 103 bis 107 Schwingspielen und der Nachgiebigkeiten unter statischer Belastung sowie der Zugfestigkeit. Alle Beanspruchungen und berechneten Größen sind nennspannungs-basiert. Grundsätzlich besteht bei Rohrprobekörpern auch die Möglichkeit eine Beanspruchung in Längs- und in Umfangsrichtung durch Innendruck zu erzeugen. Dies wird in dieser Spezifikation nicht berücksichtigt, um die Anwendung überschaubar zu halten. Bei Rohrproben mit ausgeprägter Querschnittsverkleinerung (z. B. der Prüfkörper Typ B), entsteht eine Umfangsspannung auch aufgrund einer Zugkraft (siehe Anhang C). Die Umfangsspannung muss dann mittels FEA lokal berechnet werden. Das Verfahren gilt für rohrförmige Prüfkörper deren spezifische Form den Anforderungen der Werkstoff-prüfung und bei Kurzfaserverstärkung einer hohen Vorzugsausrichtung in Probenlängsrichtung genügen. Diese DIN SPEC gilt nicht für endlosfaserverstärkte Kunststoffe. Wegen der vollkommen unterschiedlichen Fertigungstechnologien und der zu erwartenden hohen Prüflasten, sind hier die Anforderungen an die Prüfkörpergeometrie gesondert zu betrachten. Es wird nicht zielführend sein, beide Werkstoffklassen in einer Norm zu behandeln. KW - Kurzfaser-verstärkte Thermoplaste KW - Zug-Druck-Schubprüfung KW - Betriebsfestigkeit KW - Rohrprobekörper PY - 2019 DO - https://doi.org/10.31030/3085076 IS - DIN SPEC 16457:2019-12 SP - 1 EP - 58 PB - Beuth CY - Berlin AN - OPUS4-50092 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gornushkin, Igor B. A1 - Dell’Aglio, M. A1 - Motto-Ros, V. A1 - Pelascini, F. A1 - De Giacomo, A. T1 - Investigation on the material in the plasma phase by high temporally and spectrally resolved emission imaging during Pulsed Laser Ablation (PLAL) in Liquid for NPs production and consequent considerations on NPs formation N2 - In this paper experimental temperature and density maps of the laser induced plasma in water during Pulsed Laser ablation in Liquid (PLAL) for the production of metallic nanoparticles (NPs) has been determined. A detection system based on the simultaneous acquisition of two emission images at 515 and 410 nm has been constructed and the obtained images have been processed simultaneously by imaging software. The results of the data analysis show a variation of the temperature between 4000 and 7000 K over the plasma volume. Moreover, by the study of the temperature distribution and of the number densities along the plasma expansion axis it is possible to observe the condensation zone of the plasma where NPs can be formed. Finally, the time associated to the electron processes is estimated and the plasma charging effect on NPs is demonstrated. The set of observations retrieved from these experiments suggests the importance of the plasma phase for the growth of NPs and the necessity of considering the spatial distribution of plasma parameters for the understanding of one of the most important issues of the PLAL process, that is the source of solid material in the plasma phase. KW - LIBS KW - Laser induced plasma KW - Plasma modeling KW - Plasma diagnostics KW - Nanoparticle formation PY - 2019 DO - https://doi.org/10.1088/1361-6595/ab369b VL - 28 IS - 8 SP - Article Number: 085017 PB - IOP Publishing AN - OPUS4-48753 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Horn, Wolfgang A1 - Jann, Oliver A1 - Brosig, L. A1 - Müller, B. A1 - Mertes, A. A1 - de Lima Vasconcelos, S. T1 - Emissions- und geruchsarme Bauprodukte für energieeffiziente Gebäude – Entwicklung von Anforderungen und Konzepten für den Blauen Engel aus Klimaschutzsicht N2 - Menschen, die in der gemäßigten Klimazone leben, verbringen bis zu 90% ihres Lebens in Innenräumen. Deshalb hat das Innenraumklima eine sehr große Bedeutung für deren Wohlergehen, Gesundheit und Leistungsfähigkeit. In Deutschland wird ca. 40% der eingesetzten Primärenergie für das Heizen, Kühlen und Klimatisieren der Innenräume verwendet. Das Forschungsvorhaben hat eine Laufzeit vom Oktober 2013 bis März 2017. Es wird in Kooperation mit der Bundesanstalt für Materialforschung und –prüfung (BAM) und der Hochschule für Technik und Wirtschaft Berlin (HTW Berlin) durchgeführt. Die HTW Berlin koordiniert das Projekt. Die Rheinisch-Westfälische Technische Hochschule Aachen (RWTH) wird teilweise über einen Auftrag in das Projekt integriert. Ziel des Projektes ist es Baustoffe auf ihre Geruchsemissionen zu untersuchen, um Bauprodukte mit niedrigen Emissionen und Gerüchen identifizieren zu können. Den Verbraucherinnen und Verbrauchern wird somit die Möglichkeit gegeben emissions- und geruchsarme Baustoffe zu wählen. Die Aufgabenstellung des Projektes ist nachfolgend aufgeführt: Arbeitspaket 1: Geruchsmessung bei Produkten mit dem Blauen Engel (siehe Kapitel 4 und 5); Arbeitspaket 2: Untersuchung von Vergleichsmaßstäben (siehe Kapitel 6); Arbeitspaket 3: Untersuchung der Linearität der Acetonskala (siehe Kapitel 7); Arbeitspaket 4: Erstellung einer Produktdatenbank (siehe Kapitel 8). Die Geruchsuntersuchung ist in den Vergabekriterien für den „Blauen Engel“ für textile Bodenbeläge (RAL UZ-128) eingebunden worden. Aus den weiteren Untersuchungen sind für die Normung wichtige Erkenntnisse erarbeitet worden. KW - VOC Emissionen KW - Geruch KW - Bewertung KW - Innenraumluftqualtität KW - Bodenbeläge PY - 2019 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-487223 UR - https://www.umweltbundesamt.de/publikationen/emissions-geruchsarme-bauprodukte-fuer UR - https://www.umweltbundesamt.de/sites/default/files/medien/1410/publikationen/2019-08-20-texte_92-2019_emissionsarme-bauprodukte.pdf SN - 1862-4804 VL - 92 SP - 1 EP - 106 PB - Umweltbundesamt CY - Dessau-Roßlau AN - OPUS4-48722 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Brieger, C. A1 - Melke, J. A1 - van der Bosch, N. A1 - Reinholz, Uwe A1 - Riesemeier, Heinrich A1 - de Oliveira Guilherme Buzanich, Ana A1 - Krishna Kayarkatte, M. A1 - Derr, I. A1 - Schökel, A. A1 - Roth, C. ED - de Oliveira Guilherme Buzanich, Ana T1 - A combined in-situ XAS–DRIFTS study unraveling adsorbate induced changes on Pt nanoparticle structure N2 - The adsorption behavior of Platinum nanoparticles was studied for the as-received catalyst (under inert gas), under hydrogen and CO atmosphere using our newly designed in-situ cell. X-ray Absorption Spectroscopy (XAS) and Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) experiments were performed simultaneously with high data quality. Structural information and the type of adsorbate could be revealed via Extended X-ray Absorption Fine Structure (EXAFS) analysis, Δμ X-ray Absorption Near Edge Structure analysis (Δμ XANES) and in-situ DRIFTS. The as-received catalyst showed sub-surface oxygen and O(n-fold). Under CO atmosphere only CO(atop) was found. Reversible adsorbate induced changes of the Pt nanoparticle structure were derived from changes in the Pt-Pt coordination number and the corresponding bond distance. Under reducing conditions (H2, CO) a significant increase in both values occurred. Temperature dependent desorption of CO revealed a gradual shift from Pt-CO to Pt-O. Reoxidation was clearly assigned to strong metal support interaction from the SiO2 support. KW - X-ray absorption spectroscopy KW - DRIFTS KW - XANES KW - CO adsoprtion KW - Platinum KW - String metal support interaction KW - Silica support KW - Adsorbates KW - Infrared spectroscopy PY - 2016 DO - https://doi.org/10.1016/j.jcat.2016.03.034 SN - 0021-9517 VL - 339 SP - 57 EP - 67 PB - Elsevier AN - OPUS4-38367 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lutz, C. A1 - Hampel, S. A1 - Beuermann, S. A1 - Turek, T. A1 - Kunz, U. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Radtke, Martin A1 - Fittschen, U. E. A. T1 - Investigation on Vanadium Species Distribution in Nafion™ 117 after Cyclization in a Vanadium Redox Flow Battery N2 - The vanadium redox flow battery (VRFB) is currently a potential candidate for stationary energy storage. A major challenge is the unintended vanadium transport through the separator, which results in a fade of capacity. To overcome this issue, it is necessary to understand the transport processes in the membrane on a more fundamental level. In this work, the vanadium species distribution in Nafion™ 117 after cyclization was investigated. Two membranes, one from a charged VRFB and another from a discharged VRFB, were analyzed using ultraviolet–visible spectroscopy (UV/VIS) and X-ray absorption near edge structure spectroscopy (XANES). Little difference between the two membranes was recognizable according to the UV/VIS results. In comparison, the XANES results showed that the membrane from the charged VRFB contains more V3+ than VO2+, whereas for the discharged case, more VO2+ is present in the membrane. KW - Synchrotron KW - BAMline KW - XANES KW - Vanadium redox flow battery PY - 2021 VL - 64 SP - 1 EP - 8 AN - OPUS4-54144 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lin, R. A1 - Li, X. A1 - Krajnc, A. A1 - Li, Z. A1 - Li, M. A1 - Wang, W. A1 - Zhuang, L. A1 - Smart, S. A1 - Zhu, Z. A1 - Appadoo, D. A1 - Harmer, J. R. A1 - Wang, Z. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Beyer, S. A1 - Wang, L. A1 - Mali, G. A1 - Bennett, T. D. A1 - Chen, V. A1 - Hou, J. T1 - Mechanochemically Synthesised Flexible Electrodes Based on Bimetallic Metal–Organic Framework Glasses for the Oxygen Evolution Reaction N2 - The melting behaviour of metal–organic frameworks (MOFs) has aroused significant research interest in the areas of materials science, condensed matter physics and chemical engineering. This work first introduces a novel method to fabricate a bimetallic MOF glass, through meltquenching of the cobalt-based zeolitic imidazolate Framework (ZIF) [ZIF-62(Co)] with an adsorbed ferric coordination complex. The high-temperature chemically reactive ZIF-62-(Co) liquid facilitates the formation of coordinative bonds between Fe and imidazolate ligands, incorporating Fe nodes into the framework after quenching. The resultant Co–Fe bimetallic MOF glass therefore shows a significantly enhanced oxygen evolution reaction performance. The novel bimetallic MOF glass, when combined with the facile and scalable mechanochemical synthesis technique for both discrete powders and surface coatings on flexible substrates, enables significant opportunities for catalytic device Assembly KW - Electrodes KW - MOF KW - OER KW - XANES KW - XAS KW - Bimetallic frameworks PY - 2022 DO - https://doi.org/10.1002/anie.202112880 VL - 61 IS - 4 SP - e202112880 PB - Wiley AN - OPUS4-54018 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Qureshi, Navid A1 - Morrow, Ryan A1 - Eltoukhy, Samar A1 - Grinenko, Vadim A1 - de Oliveira Guilherme Buzanich, Ana A1 - Onykiienko, Yevhen A. A1 - Kulbakov, Anton A1 - Inosov, Dmytro S. A1 - Adler, Peter A1 - Valldor, Martin T1 - Noncollinear Magnetic Structures in the Chiral Antiperovskite β-Fe2SeO N2 - We present the magnetic properties of the chiral, polar, andpossibly magnetoelectric antiperovskite β-Fe2SeO as derived from magnet-ization and specific-heat measurements as well as from powder neutrondiffraction and Mössbauer experiments. Our macroscopic data unambig-uously reveal two magnetic phase transitions at TN1 ≈ 103 K and TN2 ≈ 78K, while Rietveld analysis of neutron powder diffraction data reveals anoncollinear antiferromagnetic structure featuring magnetic moments inthe a−b plane of the trigonal structure and a ferromagnetic moment alongc. The latter is allowed by symmetry between TN1 and TN2, weakly visible inthe magnetization data yet unresolvable microscopically. While theintermediate phase can be expressed in the trigonal magnetic spacegroup P31, the magnetic ground state is modulated by a propagation vectorq = (1/2 1/2 0) resulting in triclinic symmetry and an even more complexlow-temperature spin arrangement which is also reflected in the Mö ssbauer hyperfine patterns indicating additional splitting of Fesites below TN2. The complex noncollinear spin arrangements suggest interesting magnetoelectric properties of this polar magnet. KW - EXAFS KW - Antiperovskite KW - Magnetic structure PY - 2024 DO - https://doi.org/10.1021/acs.inorgchem.4c02916 SN - 0020-1669 VL - 63 IS - 48 SP - 22712 EP - 22720 PB - American Chemical Society (ACS) AN - OPUS4-63116 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zhang, Rui A1 - Russo, Patrícia A. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Jeon, Taeyeol A1 - Pinna, Nicola T1 - Hybrid organic–inorganic transition-metal phosphonates as precursors for water oxidation electrocatalysts N2 - Efficient water oxidation catalysts are required for the development of water splitting technologies. Herein, the synthesis of layered hybrid NiFephenylphosphonate compounds from metal acetylacetonate precursors and phenylphosphonic acid in benzyl alcohol, and their Oxygen evolution reaction performance in alkaline medium, are reported. The hybrid particles are formed by inorganic layers of NiO6 and FeO6 distorted octahedra separated by bilayers of the organic group, and template the Formation in situ of NiFe hydroxide nanosheets of sizes between 5 and 25 nm and thicknesses between 3 and 10 nm. X-ray absorption spectroscopy measurements suggest that the hybrid also acts as a template for the local structure of the metal sites in the active catalyst, which remain distorted after the transformation. Optimum electrocatalytic activity is achieved with the hybrid compound with a Fe content of 16%. The combination of the synergistic effect between Ni and Fe with the structural properties of the hybrid results in an efficient catalyst that generates a current density of 10 mA cm−2 at an overpotential of 240 mV, and also in a stable catalyst that operates continuously at low overpotentials for 160 h. KW - Water oxydation catalysis KW - EXAFS PY - 2017 DO - https://doi.org/10.1002/adfm.201703158 SN - 1616-301X SN - 1616-3028 VL - 27 IS - 40 SP - Article 1703158, 1 EP - 11 PB - WILEY-VCH Verlag CY - Weinheim AN - OPUS4-42783 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Ballach, F. A1 - Bartscher, M. A1 - Bellon, Carsten A1 - Borges de Oliveira, F. A1 - Braun, M. A1 - Dennerlein, F. A1 - Flessner, M. A1 - Fuchs, P. A1 - Günnewig, O. A1 - Hausotte, T. A1 - Hess, J. A1 - Kasperl, S. A1 - Kirschbaum, K. A1 - Li, K. A1 - Maass, N. A1 - Mayer, T. A1 - Orth, Anthony A1 - Reuter, T. A1 - Suppes, A. A1 - von Schmid, M. A1 - Weiß, D. T1 - Realistische Simulation realer Röntgencomputertomografie-Systeme mit basisqualifizierter Simulationssoftware – CTSimU2 BT - Abschlussbericht N2 - Das Förderprojekt CTSimU2 baute auf den Ergebnissen des Projektes CTSimU auf. Dieses Vorprojekt erarbeitete ein (Basis-)Qualifizierungsframework für Simulationssoftwares zur Anwendung bei der Röntgen-CT für dimensionelle Messungen. Dabei stand die ausreichende physikalische Korrektheit der Durchstrahlungssimulation im Vordergrund. Für die realitätsnahe Simulation einer CT-Anlage in einer Simulationssoftware (Digitales Modell) ist jedoch nicht nur die Korrektheit der Simulationssoftware selbst, sondern auch die Güte der Parametrisierung des realen CT-Systems in der Simulationssoftware entscheidend – dies stellte den Ausgangspunkt dar. Die Parametrisierung eines CT-Systems in einer Simulationssoftware lässt sich in vier Schritte unterteilen: nach der Datenaufnahme am realen CT-System folgt die Auswertung der aufgenommenen Daten für die Generierung allgemeiner Parameterangaben. Als letztes folgte die Übertragung der Parameter in die spezifischen Simulationssoftwares und die Validierung der resultierenden Simulationsparameter. Die Methodik der Datenaufnahme am CT und die Auswertung der Daten wurde in einem Werkzeugkasten allgemein beschrieben. Der dritte Schritt, die Umsetzung der Parameter, war softwarespezifisch und wurde beispielhaft mit den vorhandenen Simulationssoftwares durchgeführt. Die Validierung der Parameter war standardisierbar und konnte durch den entwickelten Test geleistet werden, auf dessen Basis die ausreichend korrekte Simulation einer realen Anlage beurteilt werden konnte. Endresultat des Projektes war ein Richtlinienentwurf (z. B. VDI/VDE 2630) zu diesem Test, der einen informativen Annex zum Stand der Technik bezüglich der Möglichkeiten zur Parameterbestimmung enthält. Mit einer Simulationssoftware, die die Basisqualifizierung aus CTSimU bestanden hat und einen Parameterdatensatz für ein reales CT-System enthält, der den Test aus CTSimU2 bestanden hat, können realistische Simulationen dieses CT-Systems möglich sein. KW - Computertomografie KW - Simulation KW - Dimensionelles Messen PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-641719 DO - https://doi.org/10.34657/21602 N1 - Dieses Projekt wurde durch die Förderrichtlinie WIPANO gefördert und durch das Bundesministerium für Wirtschaft und Klimaschutz (2022 -2025) finanziert. Der Projektträger Jülich verwaltet die Projekte der Förderrichtlinie WIPANO. SP - 1 EP - 22 PB - TIB Technische Informationsbibliothek CY - Hannover AN - OPUS4-64171 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Pessanha, Sofia A1 - Fortes, António A1 - Lopes, Marta B. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Ortega-Feliu, Inés A1 - Respaldiza, Miguel A. A1 - Gomez Tubio, Blanca A1 - Makarova, Anna A1 - Smirnov, Dmitry A1 - Kumar, Sourabh A1 - Mata, António A1 - Silveira, João T1 - Multi-technique computational assessment of fluoride uptake in enamel using PIGE, NEXAFS, and Raman spectroscopy N2 - This study explores F incorporation in enamel via PIGE, NEXAFS, and Raman spectroscopy, integrating experimental/simulated spectra. Machine Learning boosts data interpretation, offering key insights into F delivery for clinical application. KW - Simulations KW - Enamel KW - Fuorine KW - NEXAFS PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-631138 DO - https://doi.org/10.1039/D5TB00213C SN - 2050-750X SP - 1 EP - 10 PB - Royal Society of Chemistry (RSC) AN - OPUS4-63113 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Cordeiro, F. A1 - Llorente-Mirandes, T. A1 - López-Sánchez, J.F. A1 - Rubio, R. A1 - Sánchez-Agullo, A. A1 - Raber, G. A1 - Scharf, Holger A1 - Vélez, D. A1 - Devesa, V. A1 - Fiamegos, Y. A1 - Emteborg, H. A1 - Seghers, J. A1 - Robouch, P. A1 - De la Calle, M.B. T1 - Determination of total cadmium, lead, arsenic, mercury and inorganic arsenic in mushrooms: outcome of IMEP-116 and IMEP-39 N2 - The Institute for Reference Materials and Measurements (IRMM) of the Joint Research Centre (JRC), a Directorate General of the European Commission, operates the International Measurement Evaluation Program (IMEP). IMEP organises inter-laboratory comparisons in support of European Union policies. This paper presents the results of two proficiency tests (PTs): IMEP-116 and IMEP-39, organised for the determination of total Cd, Pb, As, Hg and inorganic As (iAs) in mushrooms. Participation in IMEP-116 was restricted to National Reference Laboratories (NRLs) officially appointed by national authorities in European Union member states. IMEP-39 was open to all other laboratories wishing to participate. Thirty-seven participants from 25 countries reported results in IMEP-116, and 62 laboratories from 36 countries reported for the IMEP-39 study. Both PTs were organised in support to Regulation (EC) No. 1881/2006, which sets the maximum levels for certain contaminants in food. The test item used in both PTs was a blend of mushrooms of the variety shiitake (Lentinula edodes). Five laboratories, with demonstrated measurement capability in the field, provided results to establish the assigned values (Xref). The standard uncertainties associated to the assigned values (uref) were calculated by combining the uncertainty of the characterisation (uchar) with a contribution for homogeneity (ubb) and for stability (ust), whilst uchar was calculated following ISO 13528. Laboratory results were rated with z- and zeta (ζ)-scores in accordance with ISO 13528. The standard deviation for proficiency assessment, σp, ranged from 10% to 20% depending on the analyte. The percentage of satisfactory z-scores ranged from 81% (iAs) to 97% (total Cd) in IMEP-116 and from 64% (iAs) to 84% (total Hg) in IMEP-39. KW - Inorganic arsenic KW - Trace elements KW - Mushrooms KW - Proficiency test PY - 2015 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-326092 DO - https://doi.org/10.1080/19440049.2014.966336 SN - 1944-0057 SN - 1944-0049 VL - 32 IS - 1 SP - 54 EP - 67 PB - Taylor & Francis CY - London [u.a.] AN - OPUS4-32609 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hachmöller, O. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Aichler, M. A1 - Radtke, Martin A1 - Dietrich, D. A1 - Schwamborn, K. A1 - Lutz, L. A1 - Werner, M. A1 - Sperling, M. A1 - Walch, A. A1 - Karst, U. T1 - Elemental bioimaging and speciation analysis for the investigation of Wilsons disease using μXRF and XANES N2 - A liver biopsy specimen from a Wilson’s disease (WD) patient was analyzed by means of micro-X-ray fluorescence (mXRF) spectroscopy to determine the elemental distribution. First, bench-top mXRF was utilized for a coarse scan of the sample under laboratory conditions. The resulting distribution maps of copper and iron enabled the determination of a region of interest (ROI) for further analysis. In order to obtain more detailed elemental information, this ROI was analyzed by synchrotron radiation (SR)-based mXRF with a beam size of 4 mm offering a resolution at the cellular level. Distribution maps of additional elements to copper and iron like zinc and manganese were obtained due to a higher sensitivity of SR-mXRF. In addition to this, X-ray absorption near edge structure spectroscopy (XANES) was performed to identify the oxidation states of copper in WD. This speciation analysis indicated a mixture of copper(I) and copper(II) within the WD liver tissue. KW - progressive hepatolenticular degeneration KW - mXRF Micro-X-ray fluorescence spectroscopy KW - XANES X-ray absorption near edge structure spectroscopy PY - 2016 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-360811 DO - https://doi.org/10.1039/C6MT00001K SN - 1756-5901 SN - 1756-591X PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-36081 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dubey, A. A1 - Hon Keat, C. A1 - Shvartsman, V. A1 - Yusenko, Kirill A1 - Escobar, M. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Hagemann, U. A1 - Kovalenko, S. A1 - Stächler, J. A1 - Lupascu, D. T1 - Mono-, Di-, and Tri-valent Cation Doped BiFe0.95Mn0.05O3 Nanoparticles: Ferroelectric Photocatalysts N2 - The ferroelectricity of multivalent co-doped Bismuth ferrite (BiFeO3; BFO) nanoparticles (NPs) is revealed and utilized for light photocatalysis exploiting their narrow electronic band gap. The photocatalytic activity of ferroelectric photocatalysts BiFe0.95Mn0.05O3 (BFM) NPs and mono-, di-, or tri-valent cations (Ag+, Ca2+, Dy3+; MDT) co-incorporated BFM NPs are studied under ultrasonication and in acidic conditions. We find that such doping enhances the photocatalytic activity of the ferroelectric NPs approximately three times. The correlation of the photocatalytic activity with structural, optical, and electrical properties of the doped NPs is established. The increase of spontaneous polarization by the mono- and tri-valent doping is one of the major factors in enhancing the photocatalytic performance along with other factors such as stronger light absorption in the visible range, low recombination rate of charge carriers and larger surface area of NPs. A-site doping of BFO NPs by divalent elements suppresses the polarization, whereas trivalent (Dy3+) and monovalent (Ag+) cations provide an increase of polarization. The depolarization field in these single domain NPs acts as a driving force to mitigate recombination of the photoinduced charge carriers. KW - Piezoresponse KW - Bismuth Ferrite KW - Nanoparticles KW - Photocatalysis KW - Ferroelectric KW - Polarization PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-557230 DO - https://doi.org/10.1002/adfm.202207105 SN - 1616-301X SP - 1 EP - 16 PB - Wiley AN - OPUS4-55723 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Grengg, C. A1 - Gluth, Gregor A1 - Mittermayr, F. A1 - Ukrainczyk, N. A1 - Bertmer, M. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Radtke, Martin A1 - Leis, A. A1 - Dietzel, M. T1 - Deterioration mechanism of alkali-activated materials in sulfuric acid and the influence of Cu: A micro-to-nano structural, elemental and stable isotopic multi-proxy study N2 - In this study, a multi-proxy approach combining 29Si, 27Al and 1H MAS-NMR, FEG-EPMA, XANES at the Cu K-edge and XRD analytics with hydrochemical tools such as ICP-OES analyses, oxygen-isotope signatures, and thermodynamic modelling was applied to K-silicate-activated metakaolin specimens - with and without CuSO4·5H2O addition - exposed to sulfuric acid at pH = 2 for 35 days. The results revealed a multistage deterioration mechanism governed by (i) acid diffusion, (ii) leaching of K-A-S-H, (iii) microstructural damage related to precipitation of expansive (K,Ca,Al)-sulfate-hydrate phases (iv) complete dissolution of the K-A-S-H framework, (v) and formation of silica gel in the outermost corroded regions. Copper ions were mainly located in layered spertiniite-chrysocolla-like phases in the as-cured materials. The results demonstrate an overall negative effect of Cu addition on chemical material durability, implying that the reported higher durability of Cu-doped AAM in biocorrosion environments can be best explained by bacteriostatic effects. KW - Alkali-activated materials KW - Acid resistance KW - Microbially induced corrosion KW - MIC PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-520567 DO - https://doi.org/10.1016/j.cemconres.2021.106373 SN - 0008-8846 VL - 142 SP - 1 EP - 15 PB - Elsevier CY - Oxford AN - OPUS4-52056 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lutz, C. A1 - Breuckmann, M. A1 - Hampel, S. A1 - Kreyenschmidt, M. A1 - Ke, X. A1 - Beuermann, S. A1 - Schafner, K. A1 - Turek, T. A1 - Kunz, U. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Radtke, Martin A1 - Fittschen, U. E. A. T1 - Characterization of Dimeric Vanadium Uptake and Species in Nafion™ and Novel Membranes from Vanadium Redox Flow Batteries Electrolytes N2 - A core component of energy storage systems like vanadium redox flow batteries (VRFB) is the polymer electrolyte membrane (PEM). In this work, the frequently used perfluorosulfonic-acid (PFSA) membrane Nafion™ 117 and a novel poly (vinylidene difluoride) (PVDF)-based Membrane are investigated. A well-known problem in VRFBs is the vanadium permeation through the membrane. The consequence of this so-called vanadium crossover is a severe loss of capacity. For a better understanding of vanadium transport in membranes, the uptake of vanadium ions from electrolytes containing Vdimer(IV–V) and for comparison also V(II), V(III), V(IV), and V(V) by both membranes was studied. UV/VIS spectroscopy, X-ray absorption near edge structure spectroscopy (XANES), total reflection X-ray fluorescence spectroscopy (TXRF), inductively coupled plasma optical emission spectrometry (ICP-OES), and micro X-ray fluorescence spectroscopy (microXRF) were used to determine the vanadium concentrations and the species inside the membrane. The results strongly support that Vdimer(IV–V), a dimer formed from V(IV) and V(V), enters the nanoscopic water-body of Nafion™ 117 as such. This is interesting, because as of now, only the individual ions V(IV) and V(V) were considered to be transported through the membrane. Additionally, it was found that the Vdimer(IV–V) dimer partly dissociates to the individual ions in the novel PVDF-based membrane. The Vdimer(IV–V) dimer concentration in Nafion™ was determined and compared to those of the other species. After three days of equilibration time, the concentration of the dimer is the lowest compared to the monomeric vanadium species. The concentration of vanadium in terms of the relative uptake λ = n(V)/n(SO3 ) are as follows: V(II) [λ = 0.155] > V(III) [λ = 0.137] > V(IV) [λ = 0.124] > V(V) [λ = 0.053] > Vdimer(IV–V) [λ = 0.039]. The results show that the Vdimer(IV–V) dimer Needs to be considered in addition to the other monomeric species to properly describe the transport of vanadium through Nafion™ in VRFBs. KW - MicroXRF KW - VRFB KW - PVDF-based membrane KW - UV/VIS KW - XANES KW - TXRF KW - ICP-OES PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-530676 DO - https://doi.org/10.3390/membranes11080576 VL - 11 IS - 8 SP - 576 PB - MDPI AN - OPUS4-53067 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - C. Pardo Pérez, L. A1 - Arndt, A. A1 - Stojkovikj, S. A1 - Y. Ahmet, I. A1 - T. Arens,, J. A1 - Dattila, F. A1 - Wendt, R. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Radtke, Martin A1 - Davies, V. A1 - Höflich, K. A1 - Köhnen, E. A1 - Tockhorn, P. A1 - Golnak, R. A1 - Xiao, J. A1 - Schuck, G. A1 - Wollgarten, M. A1 - López, N. A1 - T. Mayer, M. T1 - Determining Structure-Activity Relationships in Oxide Derived CuSn Catalysts During CO2 Electroreduction Using X-Ray Spectroscopy N2 - The development of earth-abundant catalysts for selective electrochemical CO2 conversion is a central challenge. Cu-Sn bimetallic catalysts can yield selective CO2 reduction toward either CO or formate. This study presents oxide-derived Cu-Sn catalysts tunable for either product and seeks to understand the synergetic effects between Cu and Sn causing these selectivity trends. The materials undergo significant transformations under CO2 reduction conditions, and their dynamic bulk and surface structures are revealed by correlating observations from multiple methods—X-ray absorption spectroscopy for in situ study, and quasi in situ X-ray photoelectron spectroscopy for surface sensitivity. For both types of catalysts, Cu transforms to metallic Cu0 under reaction conditions. However, the Sn speciation and content differ significantly between the catalyst types: the CO-selective catalysts exhibit a surface Sn content of 13 at. % predominantly present as oxidized Sn, while the formate-selective catalysts display an Sn content of ≈70 at. % consisting of both metallic Sn0 and Sn oxide species. Density functional theory simulations suggest that Snδ+ sites weaken CO adsorption, thereby enhancing CO selectivity, while Sn0 sites hinder H adsorption and promote formate production. This study reveals the complex dependence of catalyst structure, composition, and speciation with electrochemical bias in bimetallic Cu catalysts. KW - Electrochemical CO2 conversion KW - Cu catalysts KW - X-ray absorption spectroscopy PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-547116 DO - https://doi.org/10.1002/aenm.202103328 SN - 1614-6832 VL - 12 IS - 5 SP - 2103328 PB - Wiley-VCH GmbH AN - OPUS4-54711 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Brieger, C. A1 - Melke, J. A1 - van der Bosch, N. A1 - Reinholz, Uwe A1 - Riesemeier, Heinrich A1 - de Oliveira Guilherme Buzanich, Ana A1 - Krishna Kayarkatte, M. A1 - Schoeckel, A. A1 - Roth, C. T1 - A combined in-situ XAS-DRIFTS study unraveling adsorbate induced changes on the Pt nanoparticle structure N2 - The adsorption behavior of Platinum nanoparticles was studied for the as-received catalyst (under inert gas), under hydrogen and CO atmosphere using our newly designed in-situ cell. X-ray Absorption Spectroscopy (XAS) and Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) experiments were performed simultaneously with high data quality. Structural information and the type of adsorbate could be revealed via Extended X-ray Absorption Fine Structure (EXAFS) analysis, Dl X-ray Absorption Near Edge Structure analysis (Dl XANES) and in-situ DRIFTS. The as-received catalyst showed sub-surface oxygen and O(n-fold). Under CO atmosphere only CO(atop) was found. Reversible adsorbate induced changes of the Pt nanoparticle structure were derived from changes in the PtAPt coordination number and the corresponding bond distance. Under reducing conditions (H2, CO) a significant increase in both values occurred. Temperature dependent desorption of CO revealed a gradual shift from PtACO to PtAO. Reoxidation was clearly assigned to strong metal support interaction from the SiO2 support. KW - X-ray absorption spectroscopy KW - DRIFTS KW - XANES KW - CO adsorption KW - Platinum KW - Strong metal support interaction KW - Silica support KW - Adsorbates KW - Infrared spectroscopy PY - 2016 DO - https://doi.org/10.1016/j.jcat.2016.03.034 IS - 339 SP - 57 EP - 67 PB - Elsevier Inc. CY - Philadelphia, Pennsylvania, USA AN - OPUS4-35815 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lumpe, H. A1 - Menke, A. A1 - Haisch, C. A1 - Mayer, P. A1 - Kabelitz, Anke A1 - Yusenko, Kirill A1 - de Oliveira Guilherme Buzanich, Ana A1 - Block, T. A1 - Pöttgen, R. A1 - Emmerling, Franziska A1 - Daumann, L. J. T1 - The Earlier the Better: Structural Analysis and Separation of Lanthanides with Pyrroloquinoline Quinone N2 - Lanthanides (Ln) are critical raw materials, however, their mining and purification have a considerable negative environmental impact and sustainable recycling and separation strategies for these elements are needed. In this study, the precipitation and solubility behavior of Ln complexes with pyrroloquinoline quinone (PQQ), the cofactor of recently discovered lanthanide (Ln) dependent methanol Dehydrogenase (MDH) enzymes, is presented. In this context, the molecular structure of a biorelevant europium PQQ complex was for the first time elucidated outside a protein environment. The complex crystallizes as an inversion symmetric dimer, Eu2PQQ2, with binding of Eu in the biologically relevant pocket of PQQ. LnPQQ and Ln1Ln2PQQ complexes were characterized by using inductively coupled Plasma mass spectrometry (ICP-MS), infrared (IR) spectroscopy, 151Eu-Mössbauer spectroscopy, X-ray total scattering, and Extended X-ray absorption fine structure (EXAFS). It is shown that a natural enzymatic cofactor is capable to achieve Separation by precipitation of the notoriously similar, and thus difficult to separate, lanthanides to some extent. KW - Lanthanides KW - Structural Analysis KW - Separation PY - 2020 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-510821 DO - https://doi.org/10.1002/chem.202002653 SN - 0947-6539 VL - 26 SP - 1 EP - 8 PB - WILEY-VCH Verlag GmbH & co. KGaA AN - OPUS4-51082 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Santos de Freitas, M. A1 - Araghi, R. R. A1 - Brandenburg, E. A1 - Leiterer, Jork A1 - Emmerling, Franziska A1 - Folmert, K. A1 - Gerling-Driessen, U. I. M. A1 - Bardiaux, B. A1 - Böttcher, C. A1 - Pagel, K. A1 - Diehl, A. A1 - v. Berlepsch, H. A1 - Oschkinat, H. A1 - Koksch, B. T1 - The protofilament architecture of a de novo designed coiled coil-based amyloidogenic peptide N2 - Amyloid fibrils are polymers formed by proteins under specific conditions and in many cases they are related to pathogenesis, such as Parkinson’s and Alzheimer’s diseases. Their hallmark is the presence of a β-sheet structure. High resolution structural data on these systems as well as information gathered from multiple complementary analytical techniques is needed, from both a fundamental and a pharmaceutical perspective. Here, a previously reported de novo designed, pH-switchable coiled coil-based peptide that undergoes structural transitions resulting in fibril formation under physiological conditions has been exhaustively characterized by transmission electron microscopy (TEM), cryo-TEM, atomic force microscopy (AFM), wide-angle X-ray scattering (WAXS) and solid-state NMR (ssNMR). Overall, a unique 2-dimensional carpet-like assembly composed of large coexisiting ribbon-like, tubular and funnel-like structures with a clearly resolved protofilament substructure is observed. Whereas electron microscopy and scattering data point somewhat more to a hairpin model of β-fibrils, ssNMR data obtained from samples with selectively labelled peptides are in agreement with both, hairpin structures and linear arrangements. KW - Amyloid KW - Elektronenmikroskopie PY - 2018 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-458713 UR - https://www.sciencedirect.com/science/article/pii/S1047847718301333 DO - https://doi.org/10.1016/j.jsb.2018.05.009 SN - 1047-8477 VL - 203 IS - 3 SP - 263 EP - 272 PB - Elsevier AN - OPUS4-45871 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Heilmann, Maria A1 - Prinz, Carsten A1 - Bienert, Ralf A1 - Wendt, R. A1 - Kunkel, B. A1 - Radnik, Jörg A1 - Hoell, A. A1 - Wohlrab, S. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Emmerling, Franziska T1 - Size-Tunable Ni–Cu Core–Shell Nanoparticles—Structure, Composition, and Catalytic Activity for the Reverse Water–Gas Shift Reaction N2 - A facile and efficient methodology is described for the solvothermal synthesis of size-tunable, stable, and uniform NiCu core–shell nanoparticles (NPs) for application in catalysis. The diameter of the NPs is tuned in a range from 6 nm to 30 nm and to adjust the Ni:Cu ratio from 30:1 to 1:1. Furthermore, the influence of different reaction parameters on the final NPs is studied. The NPs are structurally characterized by a method combination of transmission electron microscopy, anomalous small-angle X-ray scattering, X-ray absorption fine structure, and X-ray photoelectron spectroscopy. Using these analytical methods, it is possible to elucidate a core–shell–shell structure of all particles and their chemical composition. In all cases, a depletion from the core to the shell is observed, with the core consisting of NiCu alloy, surrounded by an inner Ni-rich shell and an outer NiO shell. The SiO2-supported NiCu core–shell NPs show pronounced selectivity of >99% for CO in the catalytic reduction of CO2 to CO using hydrogen as reactant (reverse water–gas shift reaction) independent of size and Ni:Cu ratio. KW - Nanoparticles KW - Core-shell KW - Catalysis PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-543606 DO - https://doi.org/10.1002/adem.202101308 SN - 1438-1656 SP - 1 EP - 13 PB - Wiley VCH AN - OPUS4-54360 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Loges, A. A1 - Scholz, G. A1 - de Sousa Amadeu, Nader A1 - Jingjing, S. A1 - Emmerling, Franziska A1 - John, T. A1 - Paulus, B. A1 - Braun, T. T1 - Studies on the local structure of the F/OH site in topaz by magic angle spinning nuclear magnetic resonance and Raman spectroscopy N2 - he mutual influence of F and OH groups in neighboring sites in topaz (Al2SiO4(F,OH)2) was investigated using magic angle spinning nuclear magnetic resonance (MAS NMR) and Raman spectroscopy. The splitting of 19F and 1H NMR signals, as well as the OH Raman band, provides evidence for hydrogen bond formation within the crystal structure. Depending on whether a given OH group has another OH group or fluoride as its neighbor, two different hydrogen bond constellations may form: either OH···O···HO or F···H···O. The proton accepting oxygen was determined to be part of the SiO4 tetrahedron using 29Si MAS NMR. Comparison of the MAS NMR data between an OH-bearing and an OH-free topaz sample confirms that the 19F signal at −130 ppm stems from F− ions that take part in H···F bonds with a distance of ∼ 2.4 Å, whereas the main signal at −135 ppm belongs to fluoride ions with no immediate OH group neighbors. The Raman OH sub-band at 3644 cm−1 stems from OH groups neighboring other OH groups, whereas the sub-band at 3650 cm−1 stems from OH groups with fluoride neighbors, which are affected by H···F bridging. The integrated intensities of these two sub-bands do not conform to the expected ratios based on probabilistic calculations from the total OH concentration. This can be explained by a difference in the polarizability of the OH bond between the different hydrogen bond constellations or partial order or unmixing of F and OH, or a combination of both. This has implications for the quantitative interpretation of Raman data on OH bonds in general and their potential use as a probe for structural (dis-)order. No indication of tetrahedrally coordinated Al was found with 27Al MAS NMR, suggesting that the investigated samples likely have nearly ideal Al/Si ratios, making them potentially useful as high-density electron microprobe reference materials for Al and Si, as well as for F. KW - Topas KW - NMR KW - XRD PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-561863 DO - https://doi.org/10.5194/ejm-34-507-2022 SN - 1617-4011 VL - 34 IS - 5 SP - 507 EP - 521 PB - Copernicus Publications CY - Göttingen AN - OPUS4-56186 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Senges, Gene A1 - de Oliveira Guilherme Buzanich, Ana A1 - Lindič, Tilen A1 - Gully, Tyler A. A1 - Winter, Marlon A1 - Radtke, Martin A1 - Röder, Bettina A1 - Steinhauer, Simon A1 - Paulus, Beate A1 - Emmerling, Franziska A1 - Riedel, Sebastian T1 - Unravelling highly oxidized nickel centers in the anodic black film formed during the Simons process by in situ X-ray absorption near edge structure spectroscopy N2 - The electrofluorination after Simons has been used for the last century to produce everyday life materials. An in situ XANES investigation of the controversially debated black film apparent in the Simons process revealed high-valent nickel centers. KW - Synchrotron KW - BAMline KW - XANES PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-608366 DO - https://doi.org/10.1039/d3sc06081k SN - 2041-6520 VL - 15 IS - 12 SP - 4504 EP - 4509 PB - Royal Society of Chemistry (RSC) AN - OPUS4-60836 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bach, S. A1 - Visnow, E. A1 - Panthöfer, M. A1 - Gorelik, T. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Gulo, A. A1 - Kolb, U. A1 - Emmerling, Franziska A1 - Lind, C. A1 - Tremel, W. T1 - Hydrate networks under mechanical stress – A case study for Co3(PO4)2·8H2O N2 - The nature of the bound water in solids with hydrogen-bonded networks depends not only on temperature and pressure but also on the nature of the constituents. The collapse and reorientation of these network structures determines the stability of hydrated solids and transitions to other crystalline or amorphous phases. Here, we study the mechanochemically induced loss of bound water in Co₃(PO₄)₂·8H₂O and compare this process to the behavior under hydrostatic pressure. The associated phase transition and its kinetics were monitored by X-ray powder diffraction with Synchrotron radiation and quantitative IR spectroscopy. High shearing forces are responsible for the degradation of the hydrogen-bonded network and the concomitant crystalline–amorphous transformation. UV/Vis spectroscopy, extended X-ray absorption spectroscopy (EXAFS), and X-ray absorption near-edge spectroscopy (XANES) provided information about the short-range order in the amorphous solid, and thermal analysis revealed its composition and showed that the moderate charge densities of the Co²⁺ and PO₄³⁻ ions, which make the hydration enthalpy comparable to the binding energy of the counteranions, and the Formation of hydrogen-bonded networks favor multistage crystallization processes associated with the release and uptake of coordinated water. The changes of the Co²⁺ coordination induce a color change from pink to blue; therefore, Co₃(PO₄)₂·8H₂O can be used as an overheat temperature indicator. KW - Mechanochemistry KW - Amorphous materials KW - Hydrates KW - Cobalt KW - Phosphates PY - 2016 DO - https://doi.org/10.1002/ejic.201501481 SN - 1434-1948 SN - 1099-0682 VL - 2016 IS - 13-14 SP - 2072 EP - 2081 PB - Wiley-VCH Verlag GmbH & Co. KGaA CY - Weinheim, Germany AN - OPUS4-36434 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Cakir, Cafer Tufan A1 - Piotrowiak, T. A1 - Reinholz, Uwe A1 - Ludwig, A. A1 - Emmerling, Franziska A1 - Streli, C. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Radtke, Martin T1 - Exploring the Depths of Corrosion: A Novel GE-XANES Technique for Investigating Compositionally Complex Alloys N2 - In this study, we propose the use of nondestructive, depth-resolved, element-specific characterization using grazing exit X-ray absorption near-edge structure spectroscopy (GE-XANES) to investigate the corrosion process in compositionally complex alloys (CCAs). By combining grazing exit X-ray fluorescence spectroscopy (GE-XRF) geometry and a pnCCD detector, we provide a scanning-free, nondestructive, depth-resolved analysis in a sub-micrometer depth range, which is especially relevant for layered materials, such as corroded CCAs. Our setup allows for spatial and energy-resolved measurements and directly extracts the desired fluorescence line, free from scattering events and other overlapping lines. We demonstrate the potential of our approach on a compositionally complex CrCoNi alloy and a layered reference sample with known composition and specific layer thickness. Our findings indicate that this new GE-XANES approach has exciting opportunities for studying surface catalysis and corrosion processes in real-world materials. KW - Degradation mechanisms KW - Grazin exit XANES KW - Depth resolved XANES KW - Compositional complex alloys KW - Corrosion PY - 2023 DO - https://doi.org/10.1021/acs.analchem.3c00404 VL - 95 SP - 4810 EP - 4818 PB - ACS Publications AN - OPUS4-57823 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rex, Tobias A1 - Vilela, Raquel R. C. A1 - Bauer, Nadine A1 - Hepp, Alexander A1 - de Camargo, Andrea S. S. A1 - Kiefer, Friedemann A1 - Strassert, Cristian A. T1 - Host–Guest Nanoparticles Incorporating a Fluorophore-Conjugated Pt(II) Complex: A Ratiometric Dual Emitter Performing as a Self-Referenced Oxygen Reporter N2 - Ratiometric optical sensors, which provide real-time measurements by comparing the intensities of two spectrally separated emission bands, are highly effective for monitoring oxygen levels. By combining oxygen-independent and oxygensensitive emission characteristics, they offer accurate quantification, distinguishing them from other sensor types. In this work, we designed a ratiometric optical sensor concept based on a biscyclometalated platinum(II) complex coupled with an organic naphthalonitrile-based fluorophore and incorporated it into mesoporous silica nanoparticles. This encapsulation strategy significantly improved the stability and water-dispersibility of the otherwise hydrophobic coordination compound while preventing aggregation and enhancing its photophysical properties. Both the free molecule and its nanoparticle-encapsulated form were characterized, revealing high sensitivity to oxygen variations with the unique feature of self-referenced ratiometric readout. The sensor’s response was effectively measured at the single-particle level using photoluminescence microscopy, providing temporally and spatially resolved oxygen readouts. The versatility of the system was demonstrated across different experimental setups, including suspensions, solids, and agarose-embedded forms, highlighting is adaptability to a wide range of applications. This system holds significant promise for advanced oxygen monitoring, offering a reliable tool for high-resolution detection in complex environments with multiple orthogonal readouts. KW - Oxygen sensing KW - Ratiometric luminescence KW - Platinum (II) complex KW - Dual emitter probe KW - Mesoporous silica nanoprticles PY - 2026 DO - https://doi.org/10.1021/acsaom.5c00262 SN - 2771-9855 VL - 4 IS - 2 SP - 332 EP - 342 PB - American Chemical Society (ACS) AN - OPUS4-65689 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mehri Sofiani, F. A1 - Chaudhuri, Somsubhro A1 - Elahi, S. A. A1 - Wallaert, E. A1 - Depover, T. A1 - De Waele, W. T1 - Accelerated laboratory simulation of corrosion pit evolution in low-carbon steel using phase-field guided overpotential application N2 - This study is performed to replicate field data of pit geometry evolution in the laboratory by accelerating pit evolution through the application of relatively high overpotential on low-carbon steel. A phase-field model is used to reduce the number of trials and errors in the laboratory. The effect of overpotential on pitting corrosion is studied in low-carbon steel in the electrolyte representative of the North Sea. Based on the results obtained through the numerical model, potentiostatic polarisation tests are performed, and a comparison is made between such accelerated tests and steel coupons collected from the field. The results of this comparison suggest that the pitting corrosion acceleration mechanism effectively produces surface conditions closely resembling those of naturally pitted steel. Additionally, it enables the investigation of the electrochemical characteristics of a stable pit over long-term exposure, where direct probing is challenging. This framework strives to mitigate the excessive costs of time-consuming coupon experiments by correlating accelerated pitting corrosion in short periods of time with actual pitting corrosion observed over the long term. KW - Pitting corrosion KW - Corrosion acceleration KW - Potentiodynamic tests KW - Phase-field KW - S355 PY - 2025 DO - https://doi.org/10.1016/j.engfailanal.2025.110352 SN - 1350-6307 VL - 184 SP - 1 EP - 20 PB - Elsevier CY - Oxford AN - OPUS4-64805 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Sobina, E. A1 - Zimathies, Annett A1 - Prinz, Carsten A1 - Emmerling, Franziska A1 - de Santis Neves, R. A1 - Wang, H. A1 - Mizuno, K. A1 - Devoille, L. A1 - Steel, E. A1 - Ceyhan, A. A1 - Sadak, E. ED - Sobina, E. T1 - Final report of CCQM-K153 Measurement of Specific Adsorption A [mol/kg] of N-2 and Kr on nonporous SiO2 at LN temperature (to enable a traceable determination of the Specific Surface Area (BET) following ISO 9277) N2 - CCQM key comparison K-153 Measurement of Specific Adsorption A [mol/kg] of N-2 and Kr on nonporous SiO2 at LN temperature (to enable a traceable determination of the Specific Surface Area (BET) following ISO 9277) has been performed by the Surface Analysis Working Group (SAWG) of the Consultative Committee for Amount of Substance (CCQM). The objective of this key comparison is to compare the equivalency of the National Metrology Institutes (NMIs) and Designated Institutes (DIs) for the measurement of specific adsorption, BET specific surface area) of nonporous substances (sorbents, ceramics, catalytic agents, etc) used in advanced technology. In this key comparison, a commercial nonporous silicon dioxide was supplied as a sample. Eight NMIs participated in this key comparison, but only five NMI's have reported in time. All participants used a gas adsorption method, here nitrogen and (or) krypton adsorption at 77.3 K, for analysis according to the international standards ISO 15901-2 and 9277. In this key comparison, the degrees of equivalence uncertainties for specific adsorption nitrogen and krypton, BET specific surface area were established. KW - Nonporous SiO2 KW - Specific Adsorption of N-2 and Kr KW - BET specific surface area PY - 2019 DO - https://doi.org/10.1088/0026-1394/56/1A/08013 VL - 56 IS - 1A SP - 08013 PB - IOP publishing Ltd CY - Bristol, UK AN - OPUS4-50358 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dietzmann, Simon A1 - Mehmood, Asad A1 - de Oliveira Guilherme Buzanich, Ana A1 - Emmerling, Franziska A1 - Fellinger, Tim-Patrick A1 - Thomas, A. T1 - Characterization of Solid-State Complexes by XAS N2 - Atomically dispersed metal-nitrogen doped carbons (M-N-C) are promising catalysts for the activation of small molecules such as O2 and CO2. These single atom catalysts (SAC) operate at the interface between homogenous and heterogenous catalysts. Currently, many examples of M-N-C are known with good oxygen reduction reaction activity but lacking a controlled synthesis of the specific active sites of the precatalyst. Recently, our group facilitated the synthesis of pure pyrrolic M-N4 sites using Zn ions as imprinters.[1] These amorphous materials obtained by active site imprinting method are characterized at the BAMline (Bessy II) by X-ray absorption spectroscopy (XAS). In-situ/operando measurements will be crucial in future work for a better understanding of the dynamic changes of the active site. T2 - InSynX Workshop 2023 CY - Sao Paulo, Brazil DA - 06.03.2023 KW - Solid-State Complexes PY - 2023 AN - OPUS4-58933 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bernal, S. A. A1 - Angst, U. M. A1 - Provis, J. L. A1 - Thiel, C. A1 - Gluth, Gregor A1 - Villagran-Zaccardi, Y. A1 - De Belie, N. T1 - Recommendation of RILEM TC 281-CCC: RILEM CPC-18R1—guideline for measuring the carbonation depth of hardened concrete using a pH indicator solution N2 - This recommendation provides a procedure for determining the carbonation depth on the surface of concrete by applying a pH indicator. This includes definitions of carbonation, carbonation depth and carbonation front, as well as descriptions of the different pH indicator solutions that can be used. Recommendations for testing laboratory-prepared specimens and those obtained from concrete structures are also given. This involves guidelines for sample preparation and/or extraction, CO2 exposure duration, carbonation depth determination and reporting of results. A section on data interpretation is also provided, as carbonation results are used for determining durability of concrete, as well as a criterion for materials selection or for carbon uptake calculations. The new Recommendation CPC-18R1 is intended to supersede the former RILEM recommendation CPC-18, particularly when prescribed as the preferred method for evaluating and reporting carbonation depths. KW - Carbonation KW - Concrete KW - pH indicator KW - Phenolphthalein KW - Testing PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-656191 DO - https://doi.org/10.1617/s11527-026-02966-0 SN - 1359-5997 SN - 1871-6873 VL - 59 IS - 3 SP - 1 EP - 11 PB - Springer Nature AN - OPUS4-65619 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Medeiros, V.L. A1 - Goulart de Araujo, L. A1 - Ratero, D.R. A1 - Paula, A.S. A1 - Ferreira Molina, E. A1 - Jaeger, Christian A1 - Takehiro Marumo, J. T1 - Synthesis and physicochemical characterization of a novel adsorbent based on yttrium silicate: A potential material for removal of lead and cadmium from aqueous media N2 - A new metallosilicate based on yttrium was synthesized and characterized by XRD, FT-IR, 29Si MAS-NMR, and 89Y MAS-NMR. The mixed framework of the material was confirmed by the detection of distinct chemical shift groups using 29Si MAS-NMR (at -82 to -87 ppm, -91 to -94 ppm, -96 to -102 ppm, and -105 to -108 ppm), as well as four distinct chemical shifts in the 89Y MAS-NMR spectrum (at -89, -142, -160, and -220 ppm). Adsorption and kinetic analyses indicated the potential of the new material for the removal of lead and cadmium from aqueous media. The adsorption results for lead indicated that dynamic equilibrium was reached after five hours, with total lead removal of around 94 %, while for cadmium it was reached in the first hour, with total Cadmium removal of around 74 %. The adsorptions of lead and cadmium were modeled using pseudo-first order (PFO) and pseudo-second order (PSO) kinetic models. Although both models provided high R2 values (0.9903 and 0.9980, respectively), the PSO model presented a much lower χ2 red value (4.41×10−4), compared to the PFO model (2.12×10−3), which indicated that the rate-limiting step was probably due to the chemisorption of lead from the solution onto the yttrium-based metallosilicate. KW - Yttrium silicates KW - 29Si KW - 89Y MAS-NMR KW - Adsorption KW - Chemisorption KW - Cadmium and lead remediation PY - 2020 DO - https://doi.org/10.1016/j.jece.2020.103922 VL - 8 SP - 103922 PB - Elsevier Ltd. AN - OPUS4-51292 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mehri Sofiani, F A1 - Chaudhuri, Somsubhro A1 - Elahi, S.A. A1 - Hectors, K. A1 - De Waele, W. T1 - Quantitative Analysis of the Correlation between Geometric Parameters of Pits and Stress Concentration Factors for a Plate Subject to Uniaxial Tensile Stress N2 - The offshore environment is inherently corrosive. Consequently, pits may nucleate on exposed steel surfaces. Corrosion pits can be a source of crack initiation when the structure is subject to fatigue loading. The criticality of a corrosion pit with respect to the structural integrity depends on its shape and size and can be quantified using a stress concentration factor (𝐾𝑡). In this work, a parametric 3D finite element model is developed to perform stress analysis of a pitted plate subjected to uniaxial tensile stress. The model is used for an extensive parameter study in which 𝐾𝑡 is determined for various pit configurations. It is demonstrated that each one of the geometrical parameters holds a substantial influence on the location of the Most Critical Region (MCR). It is shown that 𝐾𝑡 increases as the pit gets narrower. Pits with an elliptical mouth yield higher 𝐾𝑡 values when the angle between the load direction and the pit mouth major axis increases. Moreover, 𝐾𝑡 increases with the increase in the localized thickness loss which is more pronounced for relatively wider pits. Finally, a regression model is presented for estimating 𝐾𝑡 based on the geometric parameters of a pit. KW - FEM KW - Corrosion KW - SCF KW - Pitting corrosion PY - 2023 DO - https://doi.org/10.1016/j.tafmec.2023.104081 SN - 0167-8442 VL - 127 SP - 1 EP - 27 PB - Elsevier Ltd. AN - OPUS4-58284 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mehri Sofiani, F. A1 - Tacq, J. A1 - Elahi, S.A. A1 - Chaudhuri, Somsubhro A1 - De Waele, W. T1 - A hybrid probabilistic-deterministic framework for prediction of characteristic size of corrosion pits in low-carbon steel following long-term seawater exposure N2 - A hybrid deterministic-probabilistic framework is presented that combines in-situ measurements and numerical analysis to predict the characteristic size of corrosion pits over extended periods of exposure to seawater. A probabilistic model, informed by corrosion current density and temperature data, applies a sampling method to a range of overpotential values to reflect the surface deterioration in terms of pitting. The model is calibrated and validated with pit size data obtained from corroded coupons. Results reveal a positively skewed truncated lognormal distribution of pit depths which implies a higher prevalence of smaller pit depths, corroborated both experimentally and numerically. KW - Pitting corrosion KW - Offshore structures KW - Probabilistic analysis KW - Potentiodynamic polarisation PY - 2024 DO - https://doi.org/10.1016/j.corsci.2024.112039 VL - 232 SP - 1 EP - 15 PB - Elsevier Ltd. AN - OPUS4-60693 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rodrigues, A.C.P. A1 - Österle, Werner A1 - Gradt, Thomas A1 - Azevedo, César Roberto de Farias T1 - Impact of copper nanoparticles on tribofilm formation determined by pin-on-disc tests with powder supply: Addition of artificial third body consisting of Fe3O4, Cu and graphite N2 - Copper, magnetite and graphite particles were mixed in order to observe their impact on the coefficient of friction (CoF) during pin-on-disc tests and on the tribofilm formation after testing. Pure magnetite powder provided a value of CoF of 0.4. Magnetite-copper mixtures tested at 400 °C revealed lower CoF values (~0.4) than those at room temperature (~0.6). Magnetite-graphite and magnetite-graphite-copper mixtures presented lower CoF values (~0.3). All systems formed a magnetite-based tribofilm and patches of metallic copper were found on the tribosurfaces of the mixtures containing copper. Carbon layers and graphite nanoinclusions were observed in the graphite mixtures. The incorporation of zirconia particles, a by-product of ball milling mixing, prevented the selective transfer of graphite and copper to the tribosurfaces of some of the samples. KW - Brake pad materials KW - Sliding friction KW - Transfer layer KW - Surface analysis KW - Model friction tests PY - 2017 DO - https://doi.org/10.1016/j.triboint.2017.02.014 SN - 0301-679X VL - 110 SP - 103 EP - 112 PB - Elsevier Ltd. CY - Amsterdam AN - OPUS4-40104 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Boley, N. A1 - van der Veen, A.M.H. A1 - Robouch, P. A1 - Golze, Manfred A1 - van de Kreeke, Johannes A1 - Örnemark, U. A1 - Tylee, B. T1 - Comparability of PT schemes - what did we learn from COEPT? N2 - Abstract The use of proficiency testing schemes (PTS) by laboratories as an integral part of their quality system has been increasing in recent years. Accreditation bodies, regulators and the laboratories’ customers are increasingly using results from PTS in their relationship with laboratories. There are many PTS available in Europe in analytical chemistry; EPTIS indicates over 400. The comparability of these PTS is now a real issue, as many organisers of PTS move into new markets. The COEPT project has systematically demonstrated (in four technical sectors – water, soil, food and occupational hygiene), that there are many similarities between PTS in each sector. For example, nearly all use the z-score as a performance index. One significant difference between many PTS is the value used for the term s in the z-score equation, and this gives a range of evaluations for the same data point. Despite this, the agreement between PTS in the same sector for the evaluation of data is approximately 85%. COEPT has given us a basis for establishing the comparability of PTS and showing us where further harmonisation could occur. KW - Proficiency testing KW - Comparability KW - Harmonisation PY - 2006 SN - 0949-1775 SN - 1432-0517 VL - 11 IS - 8-9 SP - 391 EP - 399 PB - Springer CY - Berlin AN - OPUS4-14162 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - de Oliveira, Rui A1 - Marques, A.T. ED - Burnett, J.K. T1 - Optical fibre sensors for acoustic emission waves detection in composites N2 - In aeronautic and space engineering, safety is a major aspect. Periodical inspections by different non-destructive testing (NDT) techniques are performed to assess the structural integrity. The accuracy of such inspection is high ly dependent on the skills of the technician. To be more efficient automated procedures independent of human decision are needed. The costs for such inspections are also significant as they require immobilisation of aircrafts. Alternative on-line structural health monitoring (SHM) procedure capable to detect, acquire, and identify damage should permit important cost reductions but also safety increase from real-time damage assessment. The increasing application of composite materials in modern aircrafts and spacecrafts permits the development of such procedure from the embedment of sensors and actuators in the structure during manufacturing. PY - 2011 SN - 978-1-61209-960-6 IS - Chapter 1 SP - 1 EP - 28 PB - Nova Science Publishers, Inc. AN - OPUS4-24302 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Hertwig, Andreas A1 - De Castro, F.A. T1 - Newsletter - Metrology for the manufacturing of thin films KW - Metrology KW - Thin films KW - Optoelectronics KW - Photovoltaics KW - Coatings technology KW - Traceability PY - 2012 UR - http://projects.npl.co.uk/optoelectronic_films/documents/EMRP%20ThinFilms_Newsletter%20Feb%202012.pdf IS - February SP - 1 EP - 4 AN - OPUS4-25505 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Elahi, Seyed Ahmad A1 - Mehri Sofiani, F. A1 - Chaudhuri, Somsubhro A1 - Balbin, J.A. A1 - Larossa, N.O. A1 - De Waele, Wim T1 - A numerical study on fatigue strength degradation due to pitting corrosion of S355 structural steel in a marine environment N2 - This study investigates the influence of pitting corrosion on the fatigue strength of S355 steel, commonly used in offshore wind support structures. A short crack microstructural model is employed to estimate the degraded fatigue strength, effectively capturing the physics of the problem with minimal input parameters. Material characterization tests provide the key mechanical properties of S355 steel. A parametric analysis is used to examine the effects of pit shape, size, and aspect ratio. A generic relationship is identified between degraded fatigue strength and pit size for various pit aspect ratios. A sensitivity analysis reveals that the pit aspect ratio significantly influences fatigue strength, with sharper pits leading to greater reductions. The threshold stress intensity factor has a moderate effect, while in-air fatigue strength and grain size have minimal impacts. A case study is performed to evaluate the fatigue strength degradation of S355 steel exposed to the North Sea environment. Findings indicate that the most severe degradation occurs in the initial years of exposure, with the degradation rate declining over time. The results align well with experimental data, offering a robust framework for assessing structural integrity in a marine environment. KW - Fatigue strength KW - Corrosion fatigue KW - Pitting corrosion KW - Short crack KW - Micromechanical model KW - S355 structural steel PY - 2025 DO - https://doi.org/10.1016/j.engfailanal.2025.109669 SN - 1873-1961 VL - 177 SP - 1 EP - 21 PB - Elsevier Ltd. AN - OPUS4-63062 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - De Souza, C.M.G. A1 - Greiser, Sebastian A1 - Garcia, E. A1 - Quarcioni, V.A. A1 - Jäger, Christian ED - Bílek, V. ED - Kersner, Z. T1 - Evaluation of pozzolanic reactivity of calcined kaolinite N2 - The need to improve the sustainability and the need for innovation in the cement industry has brought to light the practice of using additives to the cement in order to decrease CO2 emissions in industrial plants and increase the quality of cement in terms of durability and performance. Currently some additives have been employed as granulated blast furnace slag, limestone and pozzolan. The additives give mortar and concrete larger energy efficiency, gain in durability and resistance, contributing to buildings with slender structures and cheaper and durable maintenance. Besides natural pozzolan can be used artificial ones, as calcined clays, and over a range of amorphous aluminates and silicates waste, with highly reactive function as a binder material in the presence of water and calcium hydroxide. Calcined kaolinite clays were characterized using various techniques such as XRD, thermal analysis, and NMR observing 27Al and 29Si nuclei. The results showed that there is a structural modification of the samples, from crystalline to amorphous phases with the increasing of temperature in the calcination process. There is an improving in the reactivity of calcined clays by the range of 600ºC to 750ºC temperature in the reaction with calcium oxide, according to data from Chapelle test, indicating the possibility of using them as additives for cement and confirming their pozzolanic potential. T2 - NTCC2014 - International conference on non-traditional cement and concrete CY - Brno, Czech Republic DA - 16.06.2014 KW - Kaolin KW - Pozzolan KW - Calcined clays KW - Cement additive PY - 2014 SN - 978-80-214-4867-4 SP - 225 EP - 228 PB - Novpress AN - OPUS4-31225 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - De Souza, C.M.G. A1 - Greiser, Sebastian A1 - Garcia, E. A1 - Quarcioni, V.A. A1 - Jäger, Christian T1 - Evaluation of pozzolanic reactivity of calcined kaolinite N2 - The need to improve the sustainability and the need for innovation in the cement industry has brought to light the practice of using additives to the cement in order to decrease CO2 emissions in industrial plants and increase the quality of cement in terms of durability and performance. Currently some additives have been employed as granulated blast furnace slag, limestone and pozzolan. The additives give mortar and concrete larger energy efficiency, gain in durability and resistance, contributing to buildings with slender structures and cheaper and durable maintenance. Besides natural pozzolan can be used artificial ones, as calcined clays, and over a range of amorphous aluminates and silicates waste, with highly reactive function as a binder material in the presence of water and calcium hydroxide. Calcined kaolinite clays were characterized using various techniques such as XRD, thermal analysis, and NMR observing 27Al and 29Si nuclei. The results showed that there is a structural modification of the samples, from crystalline to amorphous phases with the increasing of temperature in the calcination process. There is an improving in the reactivity of calcined clays by the range of 600ºC to 750ºC temperature in the reaction with calcium oxide, according to data from Chapelle test, indicating the possibility of using them as additives for cement and confirming their pozzolanic potential. KW - Kaolin KW - Pozzolan KW - Calcined clays KW - Cement additive PY - 2014 DO - https://doi.org/10.15623/ijret.2014.0325033 SN - 2321-7308 SN - 2319-1163 VL - 3 IS - Special Issue 13 SP - 209 EP - 213 PB - eSAT Publishing House CY - Kothapatnam AN - OPUS4-38719 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - DeRose, P.C. A1 - Wang, L. A1 - Gaigalas, A.K. A1 - Kramer, G.W. A1 - Resch-Genger, Ute A1 - Panne, Ulrich ED - Resch-Genger, Ute ED - O.S. Wolfbeis, T1 - Need for and metrological approaches towards standardization of fluorescence measurements from the view of national metrology institutes N2 - The need for standardization in fluorescence measurements to improve quality assurance and to meet regulatory demands is addressed from the viewpoint of National Metrology Institutes (NMIs). Classes of fluorescence standards are defined, including instrument calibration standards for the determination and correction of instrument bias, application-specific standards based on commonly used fluorescent labels, and instrument validation standards for periodic checks of instrument performance. The need for each class of standard is addressed and on-going efforts by NMIs and others are described. Several certified reference materials (CRMs) that have recently been developed by NMIs are highlighted. These include spectral correction standards, developed independently by both NIST and BAM (Germany), and fluorescence intensity standards for flow cytometry, developed by NIST. In addition, future activities at both institutes are addressed such as the development of day-to-day intensity standards. KW - Fluorescence spectroscopy KW - Quality assurance KW - Calibration KW - Standard KW - Comparability KW - Quantification KW - Traceability KW - Radiometry KW - Emission standard KW - Fluorescent glass KW - Spectral correction KW - Spectral fluorescence standard PY - 2008 SN - 978-3-540-75206-6 DO - https://doi.org/10.1007/4243_2008_049 SN - 1617-1306 N1 - Serientitel: Springer Series on Fluorescence – Series title: Springer Series on Fluorescence VL - 5 IS - Part A SP - 33 EP - 62 PB - Springer AN - OPUS4-18996 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wilbig, Janka A1 - Borges de Oliveira, F. A1 - Obaton, A.-F. A1 - Schwentenwein, M. A1 - Rübner, Katrin A1 - Günster, Jens T1 - Defect detection in additively manufactured lattices N2 - This paper investigates fast and inexpensive measurement methods for defect detection in parts produced by Additive Manufacturing (AM) with special focus on lattice parts made of ceramics. By Lithography-based Ceramic Manufacturing, parts were built both without defects and with typical defects intentionally introduced. These defects were investigated and confirmed by industrial X-ray Computed Tomography. Alternative inexpensive methods were applied afterwards on the parts such as weighing, volume determination by Archimedes method and gas permeability measurement. The results showed, that defects resulting in around 20% of change in volume and mass could be separated from parts free of defects by determination of mass or volume. Minor defects were not detectable as they were in the range of process-related fluctuations. Permeability measurement did not allow to safely identify parts with defects. The measurement methods investigated can be easily integrated in AM process chains to support quality control. KW - Additive manufacturing KW - Quality assurance KW - Defect detection KW - Lattices KW - Ceramics PY - 2020 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-513547 DO - https://doi.org/10.1016/j.oceram.2020.100020 VL - 3 SP - 100020 PB - Elsevier Ltd. AN - OPUS4-51354 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - De Hoog, G.S. A1 - Vicente, V.A. A1 - Gorbushina, Anna T1 - The bright future of darkness - the rising power of black fungi: black yeasts, microcolonial fungi, and their relatives N2 - Black fungi are no longer viewed as neglected, rare, or exotic fungi—in fact, we now realize that they are all around us on a daily basis. In the past, we just have been looking at the wrong places, with inadequate detection tools, or with inappropriate isolation methods. In a way, the seemingly ubiquitous presence of black fungi is disturbing, reflecting one of the bright/dark contrasts of our research field: while scientists in the black yeast area all recognize the frustration of projects being rejected because of supposed societal insignificance, the general public tends to be afraid of these dangerous and omnipresent fungi. This fear dates back to 1934 when K. Kano described Hormiscium dermatitidis from a disfiguring facial infection in Japan. Since that time, many more severely mutilating and eventually fatal infections in apparently healthy people have been reported; the present issue of Mycopathologia contains another horrid example. Later, it was realized that these infections are related to diseases like chromoblastomycosis and primary cerebritis, which are already known for more than a century. Thus, severe black yeast diseases occurred long before organ transplantation was even invented, and in times when immune disorders like leukemia inevitably were rapidly followed by death. Black fungi belong to nature’s repertoire of primary pathogens, it seems, because they are able to kill healthy and immunocompetent individuals. PY - 2013 DO - https://doi.org/10.1007/s11046-013-9666-8 SN - 0369-299X SN - 0301-486X SN - 0027-5530 SN - 1573-0832 VL - 175 IS - 5-6 SP - 365 EP - 368 PB - Springer CY - Dordrecht AN - OPUS4-28869 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bender, P A1 - Balceris, C. A1 - Ludwig, F A1 - Posth, O A1 - Bogart, L. K. A1 - Szczerba, Wojciech A1 - Castro, A A1 - Nilsson, L A1 - Costo, R A1 - Gavilan, H A1 - Gonzalez-Alonso, D A1 - de Pedro, I A1 - Barquin, L. F. A1 - Johansson, C T1 - Distribution functions of magnetic nanoparticles determined by a numerical inversion method N2 - In the present study, we applied a regularized inversion method to extract the particle size, magnetic moment and relaxation-time distribution of magnetic nanoparticles from small-angle x-ray scattering (SAXS), DC magnetization (DCM) and AC susceptibility (ACS) measurements. For the measurements the particles were colloidally dispersed in water. At first approximation the particles could be assumed to be spherically shaped and homogeneously magnetized single-domain particles. As model functions for the inversion, we used the particle form factor of a sphere (SAXS), the Langevin function (DCM) and the Debye model (ACS). The extracted distributions exhibited features/peaks that could be distinctly attributed to the individually dispersed and non-interacting nanoparticles. Further analysis of these peaks enabled, in combination with a prior characterization of the particle ensemble by electron microscopy and dynamic light scattering, a detailed structural and magnetic characterization of the particles. Additionally, all three extracted distributions featured peaks, which indicated deviations of the scattering (SAXS), magnetization (DCM) or relaxation (ACS) behavior from the one expected for individually dispersed, homogeneously magnetized nanoparticles. These deviations could be mainly attributed to partial agglomeration (SAXS, DCM, ACS), uncorrelated surface spins (DCM) and/or intra-well relaxation processes (ACS). The main advantage of the numerical inversion method is that no ad hoc assumptions regarding the line shape of the extracted distribution functions are required, which enabled the detection of these contributions. We highlighted this by comparing the results with the results obtained by standard model fits, where the functional form of the distributions was a priori assumed to be log-normal shaped. KW - SAXS KW - Small-angle X-ray scattering KW - Nanoparticle PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-429373 DO - https://doi.org/10.1088/1367-2630/aa73b4 SN - 1367-2630 VL - 19 SP - 073012, 1 EP - 073012, 19 PB - IOP Publ. Ltd. AN - OPUS4-42937 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -