TY - JOUR A1 - Niederleithinger, Ernst A1 - Wang, Xin A1 - Herbrand, M. A1 - Müller, M. T1 - Processing ultrasonic data by coda wave interferometry to monitor load tests of concrete beams N2 - Ultrasonic transmission measurements have been used for decades to monitor concrete elements, mostly on a laboratory scale. Recently, coda wave interferometry (CWI), a technique adapted from seismology, was introduced to civil engineering experiments. It can be used to reveal subtle changes in concrete laboratory samples and even large structural elements without having a transducer directly at the place where the change is taking place. Here, several load tests until failure on large posttensioned concrete beams have been monitored using networks of embedded transducers. To detect subtle effects at the beginning of the experiments and cope with severe changes due to cracking close to failure, the coda wave interferometry procedures had to be modified to an adapted step-wise approach. Using this methodology, we were able to monitor stress distribution and localize large cracks by a relatively simple technique. Implementation of this approach on selected real structures might help to make decisions in infrastructure asset management. KW - Ultrasound KW - Concrete KW - Monitoring KW - Coda wave interferometry KW - Embedded transducers PY - 2018 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-452328 DO - https://doi.org/10.3390/s19010147 SN - 1424-8220 VL - 19 IS - 1 SP - Article 147, 1 EP - 13 PB - MDPI CY - Basel AN - OPUS4-45232 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Niederleithinger, Ernst A1 - Herbrand, M. A1 - Müller, M. T1 - Monitoring von Querkraftversuchen an Spannbetondurchlaufträgern mit Ultraschall und Codawelleninterferometrie T1 - Monitoring of shear tests on prestressed concrete continuous beams using ultrasound and coda wave interferometry N2 - Zusammenfassung Im Rahmen eines Forschungsvorhabens an der RWTH Aachen wurden mehrere Spannbetondurchlaufträger bis zum Versagen belastetet. Neben umfangreicher konventioneller Messtechnik wurden zusätzlich innovative Messmethoden durch die Bundesanstalt für Materialforschung und –prüfung (BAM) getestet. Darunter waren eingebettete Ultraschall-Transducer, deren Daten mit einer neuartigen Methode, der Codawelleninterferometrie (CWI), ausgewertet wurden. Dieses Verfahren detektiert auch kleinste Änderungen im Signal und in der Wellengeschwindigkeit gegenüber einer Referenzmessung. Hiermit können Belastungs- und Strukturänderungen sowie Schäden sehr viel sensibler angezeigt werden als bei konventionellen Ultraschallmessungen. Durch eine Modifikation des Verfahrens mit gleitender Referenz können aber auch starke Veränderungen im Material, wie sie bei Bruchversuchen auftreten, erfasst werden. In den Versuchen gelang es mit Netzwerken aus bis zu 20 Ultraschall-Transducern, Spannungskonzentrationen und Rissbildungen qualitativ zu detektieren und zu verfolgen, ohne dass die Sensoren direkt am Ort der Änderung angebracht sein müssen. N2 - Abstract In the framework of a research project at RWTH Aachen University, a set of large scale post-tensioned concrete continuous beams has been loaded until failure. In addition to conventional measurement techniques, innovative methods like embedded ultrasonic transducers have been applied by the Bundesanstalt für Materialforschung und -prüfung (BAM). The data acquired with theses transducers has been processed with a novel method called coda wave interferometry (CWI). This technique is able to detect even very small changes in the ultrasonic signal and in wave velocity. Loads or structural changes as well as damages can be detected with a much higher sensitivity compared to conventional measurements. Using a modification of the technique with step-wise referencing larger changes in the material can be followed as well. In the experiments, networks of up to 20 ultrasonic transducers have been used. Stress concentrations and crack formation have been detected and monitored qualitatively, without having to place the transducers directly at the place of interest. KW - Ultraschall KW - Codawelleninterferometrie KW - Brücken KW - Belastung KW - Monitoring PY - 2017 SN - 0005-6650 SN - 1436-4867 VL - 92 IS - November SP - 474 EP - 481 PB - Springer CY - Düsseldorf AN - OPUS4-42677 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Niederleithinger, Ernst A1 - Hübner, M. A1 - Amir, J. M. A1 - Müller, H. T1 - Qualitätssicherung von Pfahlwänden mit der Ultraschallmethode - eine Machbarkeitsstudie T2 - Fachtagung Bauwerksdiagnose - Praktische Anwendungen zerstörungsfreier Prüfungen und Zukunftsaufgaben CY - Berlin, Deutschland DA - 2010-02-18 KW - Bohrpfahlwand KW - Ultraschallmethode PY - 2010 SN - 978-3-940283-24-5 IS - DGZfP-BB 121 SP - 1 EP - 9 CY - Berlin AN - OPUS4-20979 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dal Molin, E. S. A1 - Henning, L. M. A1 - Müller, J. T. A1 - Smales, Glen Jacob A1 - Pauw, Brian Richard A1 - Bekheet, M. F. A1 - Gurlo, A. A1 - Simon, U. T1 - Robocasting of ordered mesoporous silica‐based monoliths: Rheological, textural, and mechanical characterization N2 - Hierarchically porous, high‐surface‐area silica materials are excellent candidates for multiple applications like catalysis and environmental remediation. Shaping these materials with additive manufacturing (AM) techniques, like robocasting, could enable their use with the benefit of on‐demand, customized shaping and maximizing performance. Herein, ordered mesoporous silica COK‐12 slurries were robocasted into monoliths, containing different ratios of uncalcined COK‐12 and sodium bentonite (0–25 wt.%). The rheology of the mixed slurries is characterized by lower flow indexes (0.69 vs. 0.32) and higher yield stresses (96 vs. 259 Pa) compared to pure COK‐12 ones. Monoliths were printed in woodpile structures and calcined at 600°C. Micro‐CT measurements showed a linear shrinkage of 25% after calcination. Mechanical characterization showed increased uniaxial strength (0.20 ± 0.07 to 1.0 ± 0.3 MPa) with increasing binder/solids ratio from 13 to 25%. The amorphous, mesoporous structure of COK‐12 was retained. The structures exhibited open porosities of 52 ± 4% and showed higher specific mesopore volumes, and increased average mesopore size (6 vs. 8 nm) compared to COK‐12. Small‐angle x‐ray scattering analysis revealed an increased lattice parameter (10.3 vs. 11.0 nm) and reduced wall thickness (3.1 nm vs. 4.1 nm) of the COK‐12 in the monoliths. These properties indicate suitability for their application as porous supports and adsorbents. KW - Industrial and Manufacturing Engineering KW - Additive manufacturing KW - OMS KW - Porous materials KW - Robocasting KW - X-ray scattering KW - MOUSE PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-582503 DO - https://doi.org/10.1002/nano.202300109 VL - 4 IS - 11-12 SP - 615 EP - 631 PB - Wiley-VCH GmbH AN - OPUS4-58250 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Deubener, J. A1 - Allix, M. A1 - Davis, M.J. A1 - Duran, A. A1 - Höche, T. A1 - Honma, T. A1 - Komatsu, T. A1 - Krüger, S. A1 - Mitra, I. A1 - Müller, Ralf A1 - Nakane, S. A1 - Pascual, M.J. A1 - Schmelzer, J.W. A1 - Zanotto, E.D. A1 - Zhou, S. T1 - Updated definition of glass-ceramics N2 - Glass-ceramics are noted for their unusual combination of properties and manifold commercialized products for consumer and specialized markets. Evolution of novel glass and ceramic processing routes, a plethora of new compositions, and unique exotic nano- and microstructures over the past 60 years led us to review the Definition of glass-ceramics. Well-established and emerging processing methods, such as co-firing, additive manufacturing, and laser patterning are analyzed concerning the core requirements of processing glass-ceramics and the Performance of the final products. In this communication, we propose a revised, updated definition of glass-ceramics, which reads “Glass-ceramics are inorganic, non-metallic materials prepared by controlled crystallization of glasses via different processing methods. They contain at least one type of functional crystalline phase and a residual glass. The volume fraction crystallized may vary from ppm to almost 100%”. KW - Glass-ceramics definition PY - 2018 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-464711 DO - https://doi.org/10.1016/j.jnoncrysol.2018.01.033 SN - 0022-3093 SN - 1873-4812 VL - 501 SP - 3 EP - 10 PB - Elsevier B.V. AN - OPUS4-46471 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Holzer, Marco A1 - Johansen, Sidsel M. A1 - Christensen, Johan F.S. A1 - Smedskjaer, Morten M. A1 - Cicconi, Maria Rita A1 - de Ligny, Dominique A1 - Müller, Ralf A1 - de Camargo, Andrea S.S. A1 - Maaß, Robert T1 - Direct connection between secondary relaxation mode and fracture toughness in alkali-aluminosilicate glasses N2 - Oxide glasses are intrinsically brittle, lacking sufficient atomic-scale mechanisms that can relax mechanical stresses in the vicinity of a propagating crack. As a result, fracture is typically well-captured by considering local bond rupture at the crack tip. Here we demonstrate that barrier energies related to the low-temperature 𝛾-relaxation mode in alkali-aluminosilicate glasses are inversely related to the fracture toughness measured via standardized three-point bending fracture experiments. This holds true for both a series with varying cations (Li, Na, K) and one with varying Li concentration. The structural rationale for this finding is gained via Raman spectroscopy. The findings suggest that a fundamental structural relaxation mode measured on bulk specimens can serve as an effective guideline for fracture toughness of oxide glasses. Data for additional silicate glasses support this conclusion. KW - Fracture toughness KW - Oxide glass KW - Mechanical properties KW - Alkali-aluminosilicate glasses KW - Internal friction PY - 2026 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-651540 DO - https://doi.org/10.1016/j.mtadv.2025.100669 SN - 2590-0498 VL - 29 SP - 1 EP - 10 PB - Elsevier Ltd. CY - Amsterdam, Niederlande AN - OPUS4-65154 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kruschwitz, Sabine A1 - Halisch, M. A1 - Prinz, Carsten A1 - Weller, Andreas A1 - Müller-Petke, M. A1 - Dlugosch, R. T1 - Towards a better understanding of electrical relaxation N2 - Other than commonly assumed the relaxation times observed in the electrical low-frequency range (1 mHz – 40 kHz) of natural porous media like sandstones and tuff stones cannot be directly related to the dominant (modal) pore throat sizes, measured (e.g.) with mercury intrusion porosimetry (MIP). Working with a great variety of sandstones from very different origins and featuring great variations in textural and chemical compositions as well as in geometrical pore space properties, it was observed that particularly samples with narrow pore throats were characterized by long (low-frequency) relaxations. These, however, can (following the current theories) be rather explained by long “characteristic length scales” in these media or low diffusion coefficients along the electrical double layer. However, there is no straightforward way (or single approved method) of getting reliable numbers for properties such as the lengths of pore throats, the diameter and length of the wide pores and their respective distributions. Consequently we follow a multi-methodical approach and combine the benefits of MIP, micro-computed tomography (μ-CT) and nuclear magnetic resonance (NMR) to achieve much deeper insight due to the different resolutions and sensitivities to either pore constrictions (throats) or wide pores. This helps us to understand, whether the observed electrical relaxation phenomena actually depend on geometric length scales or rather on other properties such as chemical composition, clay content, clay type or cation exchange capacity. In this paper, we showcase selected results of a systematic study of a total of 16 sandstones and three tuffs. Findings and the particular advantage of the used method combination are discussed and shown in detail for a representative sample selection. T2 - Annual Symposium of the Society of Core Analysts (SCA) CY - Vienna, Austria DA - 28.08.2017 KW - Electrical relaxation KW - Complex resistivity KW - Spectral induced polarization KW - Nuclear magnetic resonance KW - Mercury intrusion porosimetry KW - Pore size distribution KW - Sandstone PY - 2017 VL - SCA2017-080 SP - 1 EP - 9 AN - OPUS4-42599 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Göbel, M. A1 - Kirsch, S. A1 - Schwarze, L: A1 - Schmidt, L. A1 - Scholz, H. A1 - Haußmann, J. A1 - Klages, M. A1 - Scholta, J. A1 - Markötter, Henning A1 - Alrwashdeh, S. A1 - Manke, I. A1 - Müller, Bernd R. T1 - Transient limiting current measurements for characterization of gas diffusion layers N2 - The water management in proton exchange membrane fuel cells (PEMFC) is strongly influenced by the design of the gas diffusion layers (GDL). Limiting current measurements in small-scale cells operating at high stoichiometries are useful to determine the oxygen transport resistance. The oxygen transport resistance increases, once water condenses inside the GDL. In this study a new electrochemical method for voltage loss estimation of GDL induced oxygen transport losses are presented. This new method, referred to as “transient limiting current” (TLC), is compared with the literature method. TLC allows a direct estimation of oxygen transport resistance at an arbitrarily conditioned state. This study also presents a case study of liquid water visualization of a PEM fuel cell with varying GDLs types. With the help of quasi in-situ synchrotron X-ray computed tomography and time resolved radiography measurements we investigate appearance and distribution of liquid water inside the GDLs under limiting current conditions. KW - In-situ characterization of GDLs KW - In-situ synchrotron X-ray computed tomography KW - In-situ synchrotron X-ray radiography KW - BAMline PY - 2018 DO - https://doi.org/10.1016/j.jpowsour.2018.09.003 SN - 0378-7753 SN - 1873-2755 VL - 402 SP - 237 EP - 245 PB - Elsevier B.V. AN - OPUS4-46552 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Cant, D. J. H. A1 - Minelli, C. A1 - Sparnacci, K. A1 - Müller, Anja A1 - Kalbe, H. A1 - Stoger-Pollach, M. A1 - Unger, Wolfgang A1 - Werner, W. S. M. A1 - Shard, A. G. T1 - Surface-Energy Control and Characterization of Nanoparticle Coatings N2 - Accurate and reproducible measurement of the structure and properties of high-value nanoparticles is extremely important for their commercialization. A significant proportion of engineered nanoparticle systems consist of some form of nominally core-shell structure, whether by design or unintentionally. Often, these do not form an ideal core-shell structure, with typical deviations including polydispersity of the core or shell, uneven or incomplete shells, noncentral cores, and others. Such systems may be created with or without intent, and in either case an understanding of the conditions for formation of such particles is desirable. Precise determination of the structure, composition, size, and shell thickness of such particles can prove challenging without the use of a suitable range of characterization techniques. Here, the authors present two such polymer core-shell nanoparticle systems, consisting of polytetrafluoroethylene cores coated with a range of thicknesses of either polymethylmethacrylate or polystyrene. By consideration of surface energy, it is shown that these particles are expected to possess distinctly differing coating structures, with the polystyrene coating being incomplete. A comprehensive characterization of these systems is demonstrated, using a selection of complementary techniques including scanning electron microscopy, scanning transmission electron microscopy, thermogravimetric analysis, dynamic light scattering, differential centrifugal sedimentation, and X-ray photoelectron spectroscopy. By combining the results provided by these techniques, it is possible to achieve superior characterization and understanding of the particle structure than could be obtained by considering results separately. KW - Nanoparticles KW - Core-shell KW - XPS KW - Size KW - Thickness KW - Damage PY - 2020 DO - https://doi.org/10.1021/acs.jpcc.0c02161 VL - 124 IS - 20 SP - 11200 EP - 11211 PB - ACS CY - Washington DC AN - OPUS4-50899 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Henning, L. M. A1 - Müller, J. T. A1 - Smales, Glen Jacob A1 - Pauw, Brian Richard A1 - Schmidt, J. A1 - Bekheet, M. F. A1 - Gurlo, A. A1 - Simon, U. T1 - Hierarchically porous and mechanically stable monoliths from ordered mesoporous silica and their water filtration potential N2 - Mechanically stable structures with interconnected hierarchical porosity combine the benefits of both small and large pores, such as high surface area, pore volume, and good mass transport capabilities. Hence, lightweight micro-/meso-/macroporous monoliths are prepared from ordered mesoporous silica COK-12 by means of spark plasma sintering (SPS, S-sintering) and compared to conventionally (C-) sintered monoliths. A multi-scale model is developed to fit the small angle X-ray scattering data and obtain information on the hexagonal lattice parameters, pore sizes from the macro to the micro range, as well as the dimensions of the silica population. For both sintering techniques, the overall mesoporosity, hexagonal pore ordering, and amorphous character are preserved. The monoliths' porosity (77–49%), mesopore size (6.2–5.2 nm), pore volume (0.50–0.22 g cm-3 ), and specific surface area (451–180 m2 g-1) decrease with increasing processing temperature and pressure. While the difference in porosity is enhanced, the structural parameters between the C-and S-sintered monoliths are largely converging at 900 C, except for the mesopore size and lattice parameter, whose dimensions are more extensively preserved in the S-sintered monoliths, however, coming along with larger deviations from the theoretical lattice. Their higher mechanical properties (biaxial strength up to 49 MPa, 724 MPa HV 9.807 N) at comparable porosities and ability to withstand ultrasonic treatment and dead-end filtration up to 7 bar allow S-sintered monoliths to reach a high permeance (2634 L m-2 h-1 bar-1), permeability (1.25 x 10^-14 m2), and ability to reduce the chemical oxygen demand by 90% during filtration of a surfactant-stabilized oil in water emulsion, while indicating reasonable resistance towards fouling. KW - SAXS KW - Hierarchically porous KW - Silica KW - Water filtration PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-555928 DO - https://doi.org/10.1039/D2NA00368F SN - 2516-0230 SP - 1 EP - 17 PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-55592 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wiedensohler, A. A1 - Wiesner, A. A1 - Weinhold, K. A1 - Birmili, W. A1 - Herrmann, M. A1 - Merkel, M. A1 - Müller, T. A1 - Pfeifer, S. A1 - Schmidt, A. A1 - Tuch, T. A1 - Velarde, F. A1 - Quincey, P. A1 - Seeger, Stefan A1 - Nowak, A. T1 - Mobility particle size spectrometers: Calibration procedures and measurement uncertainties N2 - Mobility particle size spectrometers (MPSS) belong to the essential instruments in aerosol science that determine the particle number size distribution (PNSD)in the submicrometer size range. Following calibration procedures and target uncertainties against standards and reference instruments are suggested for a complete MPSS quality assurance program: a) calibration of the CPC counting efficiency curve (within 5% for the plateau counting efficiency; within 1 nm for the 50% detection efficiency diameter), b) sizing calibration of the MPSS, using a certified polystyrene latex (PSL) particle size standard at 203 nm (within 3%), c) intercomparison of the PNSD of the MPSS (within 10% and 20% of the dN/dlogDP concentration for the particle size range 20 – 200 nm and 200 to 800 nm, respectively), and d) intercomparison of the integral PNC of the MPSS (within 10%). Furthermore, following measurement uncertainties have been investigated: a) PSL particle size standards in the range from 100-500nm match within 1% after sizing calibration at 203 nm. b) Bipolar diffusion chargers based on the radioactive nuclides Kr85, Am241 and Ni63 and a new ionizer based on corona discharge follow the recommended bipolar charge distribution, while soft X-ray-based charges may alter faster than expected. c) The use of a positive high voltage supply show a 10% better performance than a negative one. d) The intercomparison of the integral PNC of an MPSS against the total number concentration is still within the target uncertainty at an ambient pressure of approximately 500 hPa. KW - Measurement uncertainties KW - Mobility particle size spectrometer (MPPS) KW - Condensation particle counter (CPC) KW - Calibration PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-425060 DO - https://doi.org/10.1080/02786826.2017.1387229 SN - 1521-7388 VL - 52 IS - 2 SP - 146 EP - 164 PB - Tailor & Francis CY - USA AN - OPUS4-42506 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Nikoonasab, Ali A1 - Müller, Thoralf A1 - Licht, M. A1 - Raupach, M. A1 - Gluth, Gregor ED - Rogge, Andreas ED - Meng, Birgit T1 - Sulfides in the pore solutions of GGBFS-containing concretes - Influence on the corrosion of reinforcing steel N2 - Steel corrosion in sulfide-containing solutions is a challenge in various environments, such as reinforced concrete structures. In concrete, sulfides are introduced by ground granulated blast-furnace slag (GGBFS), used in standard cements and alkali-activated materials (AAMs), affecting steel corrosion. This study examined steel in synthetic GGBFS-containing cement pore solutions using electrochemical techniques. Compared to Portland cement solutions, steel in sulfide-containing solutions exhibits lower open circuit potentials and polarisation resistances. Thus, Portland cement concrete corrosion assessment standards are unsuitable for GGBFScontaining concrete. T2 - 11. Jahrestagung des DAfStb mit 63. Forschungskolloquium der BAM Green Intelligent Building CY - Berlin, Germany DA - 16.10.2024 KW - Corrosion KW - Reinforcing steel PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-612963 SN - 978-3-9818564-7-7 SP - 55 EP - 59 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-61296 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Enderlein, M. A1 - Kuna, M. A1 - Ricoeur, A. A1 - Baer, Wolfram A1 - Müller, Karsten A1 - Klein, K. A1 - Winkler, H. P. T1 - Numerische Analyse des Stoßbiegeversuchs zur Ermittlung der dynamischen Bruchzähigkeit KW - Bruchmechanik KW - Finite-Elemente-Methode KW - Dynamisches J-Integral KW - 3-Punkt-Biege-Großprobe PY - 2003 SN - 0943-3473 SN - 1616-4687 IS - 235 SP - 251 EP - 260 PB - DVM CY - Berlin AN - OPUS4-32709 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Heyn, A. A1 - Müller, Thoralf A1 - Balzer, M. A1 - Fenker, M. A1 - Kappl, H. T1 - Corrosion protection mechanisms of TiMgN hard coatings on steel N2 - Hard coated steel components are used in a wide application range, mostly for protective, wear resistant and decorative purposes. Despite of these coatings being regarded as relatively dense, there is always a high risk of localized corrosion when a coated low alloyed steel component encounters a surrounding high humidity atmosphere or even an aqueous medium. An approach to enhance the corrosion properties is the addition of magnesium to physical vapor deposited hard coatings, like TiN. It has been found that there is a remarkable increase in corrosion resistance in dependence of magnesium content of the TiMgN coating and its surface properties. In this work the authors will explain the underlying corrosion protection mechanisms by means of electrochemical and analytical studies. The positive impact of magnesium in the coating relates on its preferred dissolution vs. steel. This causes the potential to shift to more negative direction with respect to the steel substrate and additionally leads to a temporarily passivation of the steel due to alkalization of the surrounding electrolyte by formation of magnesium hydroxide. T2 - 20. Werkstofftechnisches Kolloquium CY - Chemnitz, Germany DA - 14.03.2018 KW - Corrosion KW - Titanium nitride KW - PVD hard coating KW - magnesium PY - 2018 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-457117 DO - https://doi.org/10.1088/1757-899X/373/1/012009 SN - 1757-8981 VL - 373 IS - 1 SP - 012009, 1 EP - 10 PB - IOP Publishing Ltd AN - OPUS4-45711 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Prewitz, M. A1 - Gaber, M. A1 - Müller, Ralf A1 - Marotzke, C. A1 - Holtappels, Kai T1 - Polymer coated glass capillaries and structures for high-pressure hydrogen storage: Permeability and hydrogen tightness N2 - The hydrogen tightness of high-pressure hydrogen storage is a Basic criterion for long-term storage. The H2 permeation coefficients of epoxy resin and a glass lacquer were determined to enable the geometric optimization of a glass capillary storage. It was found that the curing conditions have no significant influence on the H2 permeation coefficient of resin. The H2 permeation coefficient of epoxy resin is only about three orders of Magnitude greater than that of borosilicate glass. This suggests that the initial pressure of 700 bar takes about 2.5 years to be halved in capillary array storage. Therefore, a high-pressure hydrogen storage tank based on glass capillaries is ideally suited for long-term storage in mobile applications. KW - Permeability KW - Glass capillaries KW - Coating KW - Hydrogen storage KW - Long-term calculation KW - Epoxy resin PY - 2018 DO - https://doi.org/10.1016/j.ijhydene.2017.12.092 SN - 0360-3199 VL - 43 IS - 11 SP - 5637 EP - 5644 PB - Elsevier AN - OPUS4-44327 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Müller-Mai, C.M. A1 - Berger, Georg A1 - Stiller, M. A1 - Gildenhaar, Renate A1 - Jörn, Daniela A1 - Ploska, Ute A1 - Houshmand, A. A1 - Bednarek, A. A1 - Koch, C. A1 - Knabe, C. T1 - Evaluation of degradable bone cements for percutaneous augmentation of bone defects KW - Bone defect KW - Bioactive bone cement KW - Calcium alkali orthophosphates KW - Histology KW - Histomorphometry KW - Knochendefekt KW - Bioaktiver Knochenzement KW - Calciumalkaliorthophosphat KW - Histologie KW - Histomorphometrie PY - 2010 DO - https://doi.org/10.1002/mawe.201000706 SN - 0933-5137 SN - 1521-4052 VL - 41 IS - 12 SP - 1040 EP - 1047 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-22891 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Müller, M. A1 - Kaiser, Martin A1 - Stachowski, G.M. A1 - Resch-Genger, Ute A1 - Gaponik, N. A1 - Eychmüller, A. T1 - Photoluminescence quantum yield and matrix-induced luminescence enhancement of colloidal quantum dots embedded in ionic crystals N2 - The incorporation of colloidal quantum dots (QDs) into solid matrices, especially ionic salts, holds several advantages for industrial applications. Here, we demonstrated via absolute measurements of photoluminescence quantum yields (PL-QY) that the photoluminescence of aqueous CdTe QDs can be considerably increased upon incorporation into a salt matrix with a simple crystallization procedure. Enhancement factors of up to 2.8 and a PL-QY of 50 to 80%, both in NaCl crystals and incorporated in silicone matrices, were reached. The fact that the achievable PL enhancement factors depend strongly on PL-QY of the parent QDs can be described by the change of the dielectric surrounding and the passivation of the QD surface, modifying radiative and nonradiative rate constants. Time-resolved PL measurements revealed noncorrelating PL lifetimes and PL-QY, suggesting that weakly emissive QDs of the ensemble are more affected by the enhancement mechanism, thereby influencing PL-QY and PL lifetime in a different manner. PY - 2014 DO - https://doi.org/10.1021/cm5009043 SN - 0897-4756 SN - 1520-5002 VL - 26 IS - 10 SP - 3231 EP - 3237 PB - American Chemical Society CY - Washington, DC AN - OPUS4-31074 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Müller, B. A1 - Panasková, J. A1 - Müller, D. A1 - Horn, Wolfgang A1 - Jann, Oliver A1 - Scutaru, A.M. A1 - Plehn, W. T1 - Entwicklungen der Bewertungsmethodik von Gerüchen in Innenräumen N2 - Um eine gute Luftqualität in Gebäuden zu erreichen, müssen Reinigungslasten durch Lüften aus Räumen abgeführt bzw. vermieden oder verringert werden. Wird der Luftwechsel verringert, verschlechtert sich die Raumluftqualität, und die Zufriedenheit der Nutzer nimmt ab. An Arbeitsplätzen kann es bei schlechter Luftqualität und der daraus resultierenden Unzufriedenheit zu einer geringeren Produktivität der Beschäftigten kommen. Um die Reinigungslasten und deren Wirkung auf den Raumnutzer überdas Geruchsempfinden zu verringern, ist neben einer messtechnischen Erfassung der Verunreinigungen auch eine sensorische Prüfung in Innenräumen und von Bauprodukten notwendig. In diesem Artikel wird die Entwicklung der Bewertungsmethodik von Gerüchen im Innenraum erläutert und auf Anwendungen eingegangen. KW - Geruch KW - Innenraum KW - Bauprodukte KW - Bewertung PY - 2014 SN - 2195-643X VL - 135 IS - 2 SP - 70 EP - 82 PB - DIV Deutscher Industrieverlag GmbH CY - München AN - OPUS4-32403 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schiro, G. A1 - Müller, T. A1 - Verch, G. A1 - Sommerfeld, Thomas A1 - Mauch, Tatjana A1 - Koch, Matthias A1 - Grimm, V. A1 - Müller, M.E.H. T1 - The distribution of mycotoxins in a heterogeneous wheat field in relation to microclimate, fungal and bacterial abundance N2 - Aim: To observe the variation in accumulation of Fusarium and Alternaria mycotoxins across a topographically heterogeneous field and tested biotic (fungal and bacterial abundance) and abiotic (microclimate) parameters as explanatory variables. Methods and Results: We selected a wheat field characterized by a diversified topography, to be responsible for variations in productivity and in canopy-driven microclimate. Fusarium and Alternaria mycotoxins where quantified in wheat ears at three sampling dates between flowering and harvest at 40 points. Tenuazonic acid (TeA), alternariol (AOH), alternariol monomethyl ether (AME), tentoxin (TEN), deoxynivalenol (DON), zearalenone (ZEN) and deoxynivalenol-3-Glucoside (DON.3G) were quantified. In canopy temperature, air and soil humidity were recorded for each point with data-loggers. Fusarium spp. as trichothecene producers, Alternaria spp. and fungal abundances were assessed using qPCR. Pseudomonas fluorescens bacteria were quantified with a culture based method. We only found DON, DON.3G, TeA and TEN to be ubiquitous across the whole field, while AME, AOH and ZEN were only occasionally detected. Fusarium was more abundant in spots with high soil humidity, while Alternaria in warmer and drier spots. Mycotoxins correlated differently to the observed explanatory variables: positive correlations between DON accumulation, tri 5 gene and Fusarium abundance were clearly detected. The correlations among the others observed variables, such as microclimatic conditions, varied among the sampling dates. The results of statistical model identification do not exclude that species coexistence could influence mycotoxin production. Conclusions: Fusarium and Alternaria mycotoxins accumulation varies heavily across the field and the sampling dates, providing the realism of landscapescale studies. Mycotoxin concentrations appear to be partially explained by biotic and abiotic variables. Significance and Impact of the Study: We provide a useful experimental design and useful data for understanding the dynamics of mycotoxin biosynthesis in wheat. KW - Alternaria KW - Deoxynivalenol KW - Food Safety KW - Fusarium KW - Pseudomonas fluorescens KW - Tenuazonic acid PY - 2019 DO - https://doi.org/10.1111/jam.14104 SN - 1365-2672 SN - 1364-5072 VL - 126 IS - 1 SP - 177 EP - 190 PB - Wiley AN - OPUS4-47161 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hoesl, Simone A1 - Neumann, B. A1 - Techritz, Sandra A1 - Sauter, G. A1 - Simon, R. A1 - Schlüter, H. A1 - Linscheid, M. W. A1 - Theruing, F. A1 - Müller, Larissa A1 - Jakubowski, Norbert T1 - Internal standardization of LA-ICP-MS immunoimaging via printing of universal metal spiked inks onto tissue sections N2 - Formalin-fixed paraffin-embedded (FFPE) specimen from biopsy materials are a widespread sample format for pathologists and medical researchers. Pathologists are archiving vast numbers of FFPE samples which can be stored for decades. Conventional immunohistochemical staining (IHC) of biomarkers on FFPE tissue sections is one of the most important analytical techniques for cancer diagnosis and pathology in general. However standardization for IHC samples and quality management is tedious and differs significantly from clinic to clinic. Combining established IHC staining strategies with modern mass spectrometry mediated methods would increase it`s potential and enable access of large FFPE archives for multiplexed quantitation purposes. In this work element mass spectrometry and a new ink-jet printed internal standardization approach was successfully combined with IHC staining to facilitate quantitative multiplex assays for archived FFPE samples. The printing strategy improves elemental image resolution and reproducibility of paraffin embedded breast cancer tissue sections in laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) using conventional IHC staining as a model system to investigate the new capabilities of this technique. For the internal standardization we applied a conventional CD-ink-jet printer to print a metal spiked ink onto the top of thin layer tissue sections with constant density. Printing was carried out in a direct comparison to an iodination of the tissue section as previously described as an alternative standardization method. The use of the printed internal standard allowed correction of the fluctuation during the laser ablation process and compensated instrumental drift effects. Mediated by the ink correction approach we achieved better signal-to-background-ratios (SBR) of 74 and better spatial resolution of 30 µm compared to iodination (SBR=23). This improved performance was demonstrated on tumorous areas in FFPE breast cancer tissue sections and allowing detection of Her-2 in tumorous areas of this tissue with significantly improved contrast. KW - Internal standardization KW - LA-ICP-MS KW - Immuno imaging PY - 2016 DO - https://doi.org/10.1039/c5ja00409h SN - 0267-9477 SN - 1364-5544 VL - 31 IS - 3 SP - 801 EP - 808 AN - OPUS4-35711 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Scharlach, C. A1 - Müller, Larissa A1 - Wagner, S. A1 - Kobayashi, Y. A1 - Kratz, H. A1 - Ebert, M. A1 - Jakubowski, Norbert A1 - Schellenberger, E. T1 - LA-ICP-MS allows quantitative microscopy of europium-doped iron oxide nanoparticles and is a possible alternative to ambiguous Prussian blue iron staining N2 - The development of iron oxide nanoparticles for biomedical applications requires accurate histological evaluation. Prussian blue iron staining is widely used but may be unspecific when tissues contain substantial endogenous iron. Here we tested whether microscopy by laser ablation coupled to inductively coupled plasma mass spectrometry (LA-ICP-MS) is sensitive enough to analyze accumulation of very small iron oxide particles (VSOP) doped with europium in tissue sections. KW - Atherosclerotic plaques KW - LA-ICP-MS microscopy KW - Quantification KW - Element microscopy KW - Histology PY - 2016 DO - https://doi.org/10.1166/jbn.2016.2230 SN - 1550-7033 SN - 1550-7041 VL - 12 IS - 5 SP - 1001 EP - 1010 AN - OPUS4-36189 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -