TY - JOUR A1 - Kästner, Claudia A1 - Thünemann, Andreas T1 - Catalytic reduction of 4-nitrophenol using silver nanoparticles with adjustable activity N2 - We report on the development of ultra-small core-shell silver nanoparticles synthesized by an up-scaled modification of the polyol process. It is foreseen to use these thoroughly characterized particles as reference material to compare the catalytic and biological properties of functionalized silver nanoparticles. Small-angle X-ray scattering (SAXS) analysis reveal a narrow size distribution of the silver cores with a mean radius of RC = 3.0 nm and a distribution width of 0.6 nm. Dynamic light scattering (DLS) provides a hydrodynamic radius of RH = 10.0 nm and a PDI of 0.09. The particles’ surface is covered with poly(acrylic acid) (PAA) forming a shell with a thickness of 7.0 nm, which provides colloidal stability lasting for more than six months at ambient conditions. The PAA can be easily exchanged by biomolecules to modify the surface functionality. Replacements of PAA with glutathione (GSH) and bovine serum albumin (BSA) have been performed as examples. We demonstrate that the particles effectively catalyze the reduction of 4-nitrophenol to 4-aminophenol with sodium borohydride. With PAA as stabilizer, the catalytic activity of 436 ± 24 L g⁻¹ s⁻¹ is the highest reported in literature for silver nanoparticles. GSH and BSA passivate the surface substantially resulting in a catalytic activity of 77.6 ± 0.9 and 3.47 ± 0.50 L g⁻¹ s⁻¹, respectively. KW - Silver nanoparticles KW - Catalysis KW - Reference material KW - Protein coating PY - 2016 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-370655 DO - https://doi.org/10.1021/acs.langmuir.6b01477 SN - 0743-7463 SN - 1520-5827 VL - 32 IS - 29 SP - 7383 EP - 7391 AN - OPUS4-37065 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Breßler, Ingo A1 - Pauw, Brian Richard A1 - Thünemann, Andreas T1 - McSAS: software for the retrieval of model parameter distributions from scattering patterns N2 - A user-friendly open-source Monte Carlo regression package (McSAS) is presented, which structures the analysis of small-angle scattering (SAS) using uncorrelated shape-similar particles (or scattering contributions). The underdetermined problem is solvable, provided that sufficient external information is available. Based on this, the user picks a scatterer contribution model (or 'shape') from a comprehensive library and defines variation intervals of its model parameters. A multitude of scattering contribution models are included, including prolate and oblate nanoparticles, core-shell objects, several polymer models, and a model for densely packed spheres. Most importantly, the form-free Monte Carlo nature of McSAS means it is not necessary to provide further restrictions on the mathematical form of the parameter distribution; without prior knowledge, McSAS is able to extract complex multimodal or odd-shaped parameter distributions from SAS data. When provided with data on an absolute scale with reasonable uncertainty estimates, the software outputs model parameter distributions in absolute volume fraction, and provides the modes of the distribution (e.g. mean, variance etc.). In addition to facilitating the evaluation of (series of) SAS curves, McSAS also helps in assessing the significance of the results through the addition of uncertainty estimates to the result. The McSAS software can be integrated as part of an automated reduction and analysis procedure in laboratory instruments or at synchrotron beamlines. KW - Nanotechnology KW - Nanoparticles KW - Small-angle X-ray scattering KW - SAXS PY - 2015 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-334396 DO - https://doi.org/10.1107/S1600576715007347 SN - 0021-8898 SN - 1600-5767 VL - 48 IS - 3 SP - 962 EP - 969 PB - Blackwell CY - Oxford AN - OPUS4-33439 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Szczerba, Wojciech A1 - Schott, M. A1 - Riesemeier, Heinrich A1 - Thünemann, Andreas A1 - Kurth, D.G. T1 - Thermally induced structural rearrangement of the Fe(II) coordination geometry in metallo-supramolecular polyelectrolytes N2 - Rigid rod-type metallo-supramolecular coordination polyelectrolytes with Fe(II) centres (Fe-MEPEs) are produced via the self-assembly of the ditopic ligand 1,4-bis(2,2':6',2''-terpyridine-4'-yl)benzene (tpy-ph-tpy) and Fe(II) acetate. Fe-MEPEs exhibit remarkable electrochromic properties; they change colour from blue to transparent when an electric potential is applied. This electrochemical process is generally reversible. The blue colour in the ground state is a result of a metal-to-ligand charge transfer at the Fe(II) centre ion in a quasi-octahedral geometry. When annealed at temperatures above 100 °C, the blue colour turns into green and the formerly reversible electrochromic properties are lost, even after cooling down to room temperature. The thermally induced changes in the Fe(II) coordination sphere are investigated in situ during annealing of a solid Fe-MEPE using X-ray absorption fine structure (XAFS) spectroscopy. The study reveals that the thermally induced transition is not accompanied by a redox process at the Fe(II) centre. From the detailed analysis of the XAFS spectra, the changes are attributed to structural changes in the coordination sphere of the Fe(II) site. In the low temperature state, the Fe(II) ion rests in a quasi-octahedral coordination environment surrounded by six nitrogen atoms of the pyridine rings. The axial Fe–N bond length is 1.94 Å, while the equatorial bond length amounts to 1.98 Å. In the high temperature state, the FeN6-site exhibits a distortion with the axial Fe–N bonds being shortened to 1.88 Å and the equatorial Fe–N bonds being elongated to 2.01 Å. KW - Metallo-supramolecular polyelectrolytes KW - Electrochromism KW - XANES KW - EXAFS KW - Local structure KW - Thermal stability PY - 2014 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-317331 DO - https://doi.org/10.1039/c4cp01187b SN - 1463-9076 SN - 1463-9084 VL - 16 IS - 36 SP - 19694 EP - 19701 PB - The Royal Soc. of Chemistry CY - Cambridge AN - OPUS4-31733 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Strangfeld, Christoph A1 - Wiehle, Philipp T1 - Closure of "Quantification of moisture content in earth block masonry under natural climatic conditions" N2 - In January 2025, the research paper “Quantification of moisture content in earth block masonry under natural climatic conditions” was published in Construction and Building Materials. The central theme was the moisture monitoring of a masonry wall made of unstabilised earth blocks over a period of around 18 months. The experimental results were compared to WUFI simulations, and the moisture transport in layered wall constructions was eventually studied in WUFI. Prof. Janssen discussed this publication in Construction and Building Materials. He raised concerns about the experiments and modelling of moisture transport. In this closure, the capillary adsorption coefficient was recalculated, and deviations from the initial value were quantified. Sensitivity analyses were conducted in WUFI to evaluate the influence of different water vapour resistances and water adsorption coefficients. The resulting moisture transport was then compared to material moisture profiles measured using 1H NMR relaxometry. Finally, the water adsorption behaviour of different earth materials is discussed in respect to material moisture and corresponding relative humidity. KW - Earth masonry KW - Moisture transport KW - Capillary water absorption KW - Embedded humidity sensors KW - NMR KW - WUFI KW - Material moisture KW - Water vapour diffusion resistance KW - Sustainable building materials PY - 2025 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-637569 DO - https://doi.org/10.1016/j.conbuildmat.2025.142552 SN - 0950-0618 VL - 491 SP - 1 EP - 6 PB - Elsevier Ltd. AN - OPUS4-63756 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wolf, S. A1 - McMahon, Dino Peter A1 - Lim, K.S. A1 - Pull, C.D. A1 - Clark, S.J. A1 - Paxton, R.J. A1 - Osborne, J.L. T1 - So near and yet so far: harmonic radar reveals reduced homing ability of Nosema infected honeybees N2 - Pathogens may gain a fitness advantage through manipulation of the behaviour of their hosts. Likewise, host behavioural changes can be a defence mechanism, counteracting the impact of pathogens on host fitness. We apply harmonic radar technology to characterize the impact of an emerging pathogen - Nosema ceranae (Microsporidia) - on honeybee (Apis mellifera) flight and orientation performance in the field. Honeybees are the most important commercial pollinators. Emerging diseases have been proposed to play a prominent role in colony decline, partly through sub-lethal behavioural manipulation of their hosts. We found that homing success was significantly reduced in diseased (65.8%) versus healthy foragers (92.5%). Although lost bees had significantly reduced continuous flight times and prolonged resting times, other flight characteristics and navigational abilities showed no significant difference between infected and non-infected bees. Our results suggest that infected bees express normal flight characteristics but are constrained in their homing ability, potentially compromising the colony by reducing its resource inputs, but also counteracting the intra-colony spread of infection. We provide the first high-resolution analysis of sub-lethal effects of an emerging disease on insect flight behaviour. The potential causes and the implications for both host and parasite are discussed. PY - 2014 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-328827 DO - https://doi.org/10.1371/journal.pone.0103989 SN - 1932-6203 VL - 9 IS - 8 SP - e103989, 1 EP - 15 PB - PubMed Central AN - OPUS4-32882 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mirtschin, Nikolaus A1 - Pretsch, Thorsten T1 - Designing temperature-memory effects in semicrystalline polyurethane N2 - Temperature-memory polymers are able to generate a substantial mechanical response when heated above the temperature, at which a preceding deformation was carried out. Here we show how to design the temperature-memory effect (TME) by thermomechanical treatment. As a model polymer, phase segregated poly(ester urethane) (PEU) containing crystallizable segments of poly(1,4-butylene adipate) (PBA) was used. For programming, strain elongation was applied at temperatures within the PBA melting transition area, before temperature holding, unloading and cooling were carried out. Upon heating under stress-free or constant strain recovery conditions, precisely set temperature-memory onsets could be witnessed. Most importantly, strain fixities and recoverabilities the same as maximum recovery stresses turned out to be controllable by strain rate and temperature holding time after deformation, while transition temperatures remained largely unaffected. The tailoring of thermoresponsiveness was structurally enabled by different PBA crystallinities in the programmed state as verified by wide-angle X-ray scattering (WAXS). The reported studies intend to design TMEs in semicrystalline polyurethanes according to user-defined needs to make this technology broadly applicable. KW - Poly(ester urethane) KW - Shape memory polymer KW - Temperature-memory effect KW - Thermo-responsiveness KW - Temperature-memory polymer KW - Programming KW - Thermomechanical properties PY - 2015 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-332856 DO - https://doi.org/10.1039/c5ra05492c SN - 2046-2069 VL - 5 IS - 57 SP - 46307 EP - 46315 PB - RSC Publishing CY - London AN - OPUS4-33285 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ehlert, Christopher A1 - Unger, Wolfgang A1 - Saalfrank, P. T1 - C K-edge NEXAFS spectra of graphene with physical and chemical defects: a study based on density functional theory N2 - Recently, C K-edge Near Edge X-ray Absorption Fine Structure (NEXAFS) spectra of graphite (HOPG) surfaces have been measured for the pristine material, and for HOPG treated with either bromine or krypton plasmas (Lippitz et al., Surf. Sci., 2013, 611, L1). Changes of the NEXAFS spectra characteristic for physical (krypton) and/or chemical/physical modifications of the surface (bromine) upon plasma treatment were observed. Their molecular origin, however, remained elusive. In this work we study by density functional theory, the effects of selected point and line defects as well as chemical modifications on NEXAFS carbon K-edge spectra of single graphene layers. For Br-treated surfaces, also Br 3d X-ray Photoelectron Spectra (XPS) are simulated by a cluster approach, to identify possible chemical modifications. We observe that some of the defects related to plasma treatment lead to characteristic changes of NEXAFS spectra, similar to those in experiment. Theory provides possible microscopic origins for these changes. KW - Graphene KW - NEXAFS KW - Spectrum simulation KW - Density functional theory PY - 2014 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-309658 DO - https://doi.org/10.1039/c4cp01106f SN - 1463-9076 SN - 1463-9084 VL - 16 IS - 27 SP - 14083 EP - 14095 PB - The Royal Soc. of Chemistry CY - Cambridge AN - OPUS4-30965 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 - Hemmann, Felix A1 - Jäger, Christian A1 - Kemnitz, E. T1 - Comparison of acidic site quantification methods for a series of nanoscopic aluminium hydroxide fluorides N2 - Quantitative determination of acidic surface sites is highly important for the characterization of solid acids because the activity of a catalyst is often related to the concentration of these sites. A recently developed method using 15N Nuclear Magnetic Resonance spectroscopy (NMR) for the quantification of acidic Lewis and Brønsted sites has been tested for a series of nanoscopic aluminum hydroxide fluorides. Comparison with other methods for the quantitative determination of acidic sites shows that this 15N NMR quantification method is a promising technique for the comprehensive investigation of acidic sites. Three different acidic sites, one Brønsted and two Lewis sites, can be distinguished by their 15N chemical shifts of pyridine and simultaneously quantified under conditions corresponding to catalytic reaction conditions. Determination of the individual concentrations of acidic sites allows further insight into the catalytic process. It was found that the concentration of Brønsted sites correlates with catalyzed conversion of citronellal to isopulegol in the investigated series of catalysts. Additionally, investigations indicate that one of the Lewis sites become blocked during the reaction of citronellal. KW - Solid acids KW - TOF KW - NH3-TPD KW - Progressive catalyst poisoning KW - FTIR KW - Quantitative NMR KW - Solid state NMR PY - 2014 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-323280 DO - https://doi.org/10.1039/c4ra09477h SN - 2046-2069 VL - 4 IS - 100 SP - 56900 EP - 56909 PB - RSC Publishing CY - London AN - OPUS4-32328 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wiggenhauser, Herbert A1 - Naus, D.J. T1 - NDE of thick and highly reinforced concrete structures: state of the art N2 - The objective of the report is to present the state-of-the art of non-destructive testing methods and technologies for the inspection of thick, heavily-reinforced structures, (e.g. found in nuclear power plants). Wall thicknesses can be in excess of one meter and the structures often have increased steel reinforcement density. The accessibility for any testing method may be limited due to the presence of liners and other components such as cast-in-place items. Testing methods have to provide solutions for tasks such as locating failure (inclusions, corrosion, voids, delaminations) in the structures or the assessment of the condition of the structure in general. KW - Non-destructuive testing KW - Inspection KW - Nuclear power plant KW - State-of-the-art KW - Highly reinforced concrete KW - NDE KW - Engineering PY - 2014 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-329674 DO - https://doi.org/10.1016/j.proeng.2014.11.055 SN - 1877-7058 VL - 86 SP - 420 EP - 426 PB - Elsevier CY - Amsterdam [u.a.] AN - OPUS4-32967 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ressnig, A. A1 - Corbiere, T. A1 - Lunkenbein, T. A1 - Braun, Ulrike A1 - Willinger, M. G. A1 - Antonietti, M. T1 - Decomposition synthesis of tuneable, macroporous carbon foams from crystalline precursors via in situ templating N2 - A flexible, sustainable, one-step thermal decomposition route for the synthesis of hierarchical, heteroatom doped carbon foams is presented. Task-specific semi-organic crystals combine functions for three different purposes: the carbon and heteroatom source, a foaming agent (CO2) and an in situ generable template (NaCl). Insights to the decomposition pathway were gained through FTIR/MS coupled TGA and an ultrafast out-of-furnace heating procedure and the products were analysed with (HR)SEM/TEM, EELS, FTIR, and N2 sorption. The resulting macroporous carbon foams are excellent supports for metallic nanoparticles due to their hierarchical structure, high surface area and tuneable heteroatom contents. This was demonstrated for catalytically active copper or the magnetic CoNi alloy for water purification. KW - macroporous carbon KW - thermal decomposition KW - synthesize heteroatom KW - in situ template (NaCl) PY - 2014 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-318641 DO - https://doi.org/10.1039/c4ta03646h SN - 2050-7496 SN - 2050-7488 VL - 2 IS - 42 SP - 18076 EP - 18081 PB - RSC CY - London [u.a.] AN - OPUS4-31864 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rosemann, Paul A1 - Müller, C. A1 - Baumann, O. A1 - Modersohn, W. A1 - Halle, T. T1 - Influence of the post-weld surface treatment on the corrosion resistance of the duplex stainless steel 1.4062 N2 - The duplex stainless steel 1.4062 (X2CrNiN22-2) is used as alternative material to austenitic stainless steels in the construction industry. The corrosion resistance of welded seams is influenced by the base material, the weld filler material, the welding process and also by the final surface treatment. The scale layer next to the weld seam can be removed by grinding, pickling, electro-polished or blasting depending on the application and the requested corrosion resistance. Blasted surfaces are often used in industrial practice due to the easier and cheaper manufacturing process compared to pickled or electro-polished surfaces. Furthermore blasting with corundum-grain is more effective than blasting with glass-beads which also lower the process costs. In recent years, stainless steel surfaces showed an unusually high susceptibility to pitting corrosion after grinding with corundum. For this reason, it is now also questioned critically whether the corrosion resistance is influenced by the applied blasting agent. This question was specifically investigated by comparing grinded, pickled, corundum-grain- and glass-bead-blasted welding seams. Results of the SEM analyses of the blasting agents and the blasted surfaces will be presented and correlated with the different performed corrosion tests (potential measurement, KorroPad-test and pitting potential) on welding seams with different surface treatments. T2 - 19th Chemnitz Seminar on Materials Engineering – 19. Werkstofftechnisches Kolloquium CY - Chemnitz, Germany DA - 16.03.2017 KW - Corrosion resistance KW - Welding KW - Duplex stainless steels KW - Pitting corrosion KW - Surface treatment PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-395374 DO - https://doi.org/10.1088/1757-899X/181/1/012019 SN - 1757-899X SN - 1757-8981 VL - 181 IS - Conference 1 SP - Article UNSP 012019, 1 EP - 9 PB - IOP Publishing CY - Bristol, UK AN - OPUS4-39537 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ecker, Melanie A1 - Pretsch, Thorsten T1 - Novel design approaches for multifunctional information carriers N2 - Two design approaches for multifunctional information carriers are introduced. In the first one, quick response (QR) code carriers, which were composed of poly(ester urethane) (PEU) and microencapsulated thermochromic pigments (T-PIGs), differing in color and color switching temperature (CST), were prepared. The obtained material systems exhibited machine-readable QR codes at 23 °C and a two-stage decolorization when heated, culminating in unreadable QR codes at temperatures above the highest CST of the employed T-PIGs. In the second scenario, information carriers were sealed with a dark, thermochromic PEU layer. As a result, the QR codes were hidden at 23 °C and became readable upon heating due to color fading. Beyond the characterization of the employed components, preparation methods, functionality analyses and durability investigations are reported. When heated after thermo-mechanical programming, pronounced shape memory properties could be verified. The thermo-responsiveness of such multifunctional material systems may qualify them for usage in anti-counterfeiting applications. KW - Poly(ester urethane) KW - Shape memory polymer KW - Thermo-responsiveness KW - Information carrier KW - QR code carrier KW - Thermochromic properties KW - Microencapsulated thermochromic pigments KW - Anti-counterfeiting KW - Smart label KW - Difficult-to-copy KW - Durability KW - Multifuncitonal material systems PY - 2014 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-315176 DO - https://doi.org/10.1039/c4ra08977d SN - 2046-2069 VL - 4 IS - 87 SP - 46680 EP - 46688 PB - RSC Publishing CY - London AN - OPUS4-31517 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Buckle, T. A1 - van der Wal, S. A1 - van Malderen, S. A1 - Müller, Larissa A1 - Kuil, J. A1 - van Unen, V. A1 - Peters, R. A1 - van Bemmel, M. A1 - McDonnell, L. A1 - Velders, A. A1 - Koning, F. A1 - Vanhaeke, F. A1 - van Leeuwen, F. T1 - Hybrid imaging labels: providing the link between mass spectrometry-based molecular pathology and theranostics N2 - Development of theranostic concepts that include inductively coupled plasma mass spectrometry (ICP-MS) and laser ablation ICP-MS (LA-ICP-MS) imaging can be hindered by the lack of a direct comparison to more standardly used methods for in vitro and in vivo evaluation; e.g. fluorescence or nuclear medicine. In this study a bimodal (or rather, hybrid) tracer that contains both a fluorescent dye and a chelate was used to evaluate the existence of a direct link between mass spectrometry (MS) and in vitro and in vivo molecular imaging findings using fluorescence and radioisotopes. At the same time, the hybrid label was used to determine whether the use of a single isotope label would allow for MS-based diagnostics. KW - Imaging KW - Laser Ablation ICP-MS KW - Diagnostics PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-396813 DO - https://doi.org/10.7150/thno.17484 VL - 7 IS - 3 SP - 624 EP - 633 PB - IvySpring AN - OPUS4-39681 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kupsch, Andreas A1 - Lange, Axel A1 - Hentschel, Manfred P. A1 - Grothausmann, R. A1 - Manke, I. T1 - Verbesserte Elektronen-Tomographie mittels DIRECTT-Algorithmus N2 - Tomographische Messungen in Transmissions-Elektronenmikroskopen beziehen ihren Reiz aus der hohen Ortsauflösung im Nanometerbereich. Allerdings bringen sie neben dem hohen Aufwand bei der Probenpräparation auch eine außerordentliche Häufung von Restriktionen der Messung mit sich, die bei Verwendung herkömmlicher Rekonstruktionsalgorithmen zu erheblichen Artefakten führen. Diese Restriktionen betreffen: partielle Nichtdurchstrahlbarkeit, einen eingeschränkten Winkelbereich, wenige Projektionen in Bezug auf die Detektorgröße, Probenabbildungen größer als der Detektor, instabile Rotationsachse, variierende Winkelinkremente sowie Probenveränderungen während der Messung. Der DIRECTT-Algorithmus (Direkte iterative Rekonstruktion computertomographischer Trajektorien) kann, abgesehen von der Probenveränderung, sämtliche dieser Restriktionen geeignet berücksichtigen. Die auftretenden, teils unvollständigen Bahnen lassen sich mittels einer Treffertabelle und geeigneter Auswahl iterativ behandeln. Außerdem kann das Rekonstruktionsvolumen über die Detektorlänge hinaus erweitert werden. Damit gelingt eine weitgehende Unterdrückung von Rekonstruktionsartefakten, insbesondere der sonst dominanten Streifenartefakte, und eine deutliche Erhöhung der Ortsauflösung. Die Verbesserung der Rekonstruktionsqualität wird anhand von Modell- und experimentellen Daten gezeigt. T2 - DGZfP-Jahrestagung 2011 CY - Bremen, Germany DA - 30.05.2011 KW - Elektronen-Tomographie KW - Computer-Tomographie KW - Rekonstruktionsalgorithmen PY - 2011 SN - 978-3-940283-33-7 IS - DGZfP-BB 127 (P8) SP - 1 EP - 7 PB - Deutsche Gesellschaft für Zerstörungsfreie Prüfung (DGZfP) AN - OPUS4-25004 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Unnikrishnakurup, Sreedhar A1 - Myrach, Philipp A1 - Polomski, Benjamin A1 - Le Claire, Elisabeth A1 - Vengara, N. A1 - Balasubramaniam, Krishnan A1 - Ziegler, Mathias T1 - Thermographic crack detection in hot steel surfaces N2 - The detection and characterization of surface cracks in steel specimens prior to damage is a technologically and economically highly significant task and is of utmost importance when it comes to safety-relevant structures. In steel production where steel billets at high temperatures have to be inspected while moving a number of well-established NDT methods cannot be applied. Laser thermography however is a promising candidate to serve as a fast, non-contact and remote tool in this case. We present a study that shows that the crack detection capabilities of laser thermography can be extended also to specimens at high temperature. A combination of inductive and laser heating allows to systematically study the contrast formation as well as the optimization of the important measurement parameters. The experiments are accompanied by FEM simulations that provide a better insight of the physical correlations and support the experimental developments. The aim of these studies is to develop a system with high inspection speed and detection performance to be in-line operated under the hostile environment of steel production lines. T2 - 19th World Conference on Non-Destructive Testing (WCNDT 2016) CY - Munich, Germany DA - 13.06.2016 KW - In-line Monitoring KW - Laser Infrared thermography KW - Cracks KW - Induction heating KW - Steel billets KW - FEM simulation PY - 2016 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-389161 UR - http://ndt.net/?id=19573 SN - 1435-4934 VL - 21 IS - 7 SP - 1 EP - 8 PB - NDT.net CY - Kirchwald AN - OPUS4-38916 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jonietz, Florian A1 - Ziegler, Mathias A1 - Myrach, Philipp A1 - Suwala, H. A1 - Rethmeier, Michael T1 - Untersuchung von Punktschweißverbindungen mit aktiver Thermografie N2 - Widerstandspunktschweißen ist insbesondere im Automobilbau eine der wichtigsten Fügetechniken. Bislang erfolgt die Qualitätssicherung überwiegend durch stichprobenartige zerstörende Prüfung. Eine zerstörungsfreie Prüftechnik würde neben der Reduzierung der Prüfkosten auch eine Optimierung des Punktschweißverfahrens bedeuten, da prinzipiell jeder Schweißpunkt geprüft werden könnte und somit auch eine Reduzierung der Anzahl der Schweißpunkte möglich ist. Es wird ein Verfahren vorgestellt, bei dem die Punktschweißverbindung zwischen zwei Stahlblechen optisch auf einer Blechseite mittels Laser oder Blitzlicht erwärmt wird. Die aufgeschmolzene Zone, die sogenannte Schweißlinse, stellt dabei neben der mechanischen Verbindung auch eine Wärmebrücke zwischen den beiden verschweißten Blechen dar, die bei diesem Verfahren ausgenutzt wird. Durch den verbesserten thermischen Kontakt zwischen den verschweißten Blechen an der Schweißlinse kontrastiert diese deutlich mit dem umgebenden Blechmaterial, bei dem der Wärmeübertrag zwischen den Blechen vergleichsweise gering ist. Dieser Kontrast im thermischen Verhalten kann mittels zeitabhängiger Thermografie gemessen werden. Durch das hier vorgestellte Verfahren kann mittels aktiver Thermografie sowohl in Transmissions- als auch in Reflexionsanordnung die Größe des thermischen Kontaktes zwischen den beiden Blechen ermittelt werden, welche ein Maß für die Größe der Schweißlinse und damit für die qualitative Güte der Schweißung darstellt. Ein Vorteil des entwickelten Verfahrens ist seine Anwendbarkeit auf Bleche ohne Oberflächenbehandlung. T2 - DACH-Jahrestagung 2015 CY - Salzburg, Austria DA - 11.05.2015 PY - 2015 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-343476 UR - http://www.ndt.net/?id=19068 SN - 1435-4934 VL - 21 IS - 4 SP - 1 EP - 7 PB - NDT.net CY - Kirchwald AN - OPUS4-34347 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kuroiwa, T. A1 - Zhu, Y. A1 - Inagaki, K. A1 - Long, S. A1 - Christopher, S. A1 - Puelles, M. A1 - Porinsky, M. A1 - Hatamleh, N. A1 - Murby, J. A1 - Merrick, J. A1 - White, I. A1 - Saxby, D. A1 - Caciano de Sena, R. A1 - Dominguez de Almeida, M. A1 - Vogl, Jochen A1 - Phukphatthanachai, Pranee A1 - Fung, W.-H. A1 - Yau, H.-P. A1 - Okumu, T. O. A1 - Kang'iri, J. N. A1 - Tellez, J. A. S. A1 - Campos, E. Z. A1 - Galvan, E. C. A1 - Kaewkhomdee, N. A1 - Taebunpakul, S. A1 - Thiengmanee, U. A1 - Yafa, C. A1 - Tokman, N. A1 - Tunc, M. A1 - Can, S. Z. T1 - Report of the CCQM-K123: trace elements in biodiesel fuel N2 - The CCQM-K123 key comparison was organized by the Inorganic Analysis Working Group (IAWG) of CCQM to assess and document the capabilities of the national metrology institutes (NMIs) or the designated institutes (DIs) to measure the mass fractions of sodium, calcium, potassium, magnesium phosphorous and sulfur in biodiesel fuel (BDF). The National Metrology Institute of Japan (NMIJ) and National Institute of Standards and Technology (NIST) acted as the coordinating laboratories. Results were submitted by 11 NMIs and DIs. The participants used different measurement methods, though most of them used inductively coupled plasma-mass spectrometry (ICP-MS), isotope dilution technique with ICP-MS and inductively coupled plasma-optical emission spectrometry (ICP-OES) with microwave acid digestion. The material was quite challenging and a number of questions were raised at the IAWG meeting. Concerning S, the variation in S results between participants, particularly those using IDMS methods was discussed at the IAWG meeting. BAM, NIST and NMIJ reviewed their experimental conditions, results and/or uncertainty calculations for IDMS. According to the additional evaluation and investigation, the variances between the revised results became smaller than the original one, the revised results were overlapping between IDMS measurements of S content at the k=2 level. It is not possible to calculate a KCRV with values being modified after submission. It was concluded that this KC does not support S measurements. Accounting for relative expanded uncertainty, comparability of measurement results for each of Na, Ca, K, Mg and P was successfully demonstrated by the participating NMIs or DIs. It is expected that sodium, calcium, potassium, magnesium and phosphorus at mass fractions greater than approximately 0.1 mg/kg, 0.1 mg/kg, 0.05 mg/kg, 0.05 mg/kg and 0.1 mg/kg respectively in biodiesel fuel and similar matrices (fuels and oils etc.) can be determined by each participant using the same technique(s) employed for this key comparison to achieve similar uncertainties mentioned in the present report. Furthermore, the results of this key comparison can be utilized along with the IAWG core capability approach. KW - Biodiesel KW - Fuel KW - Sulphur KW - Reference measurement PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-393941 UR - http://iopscience.iop.org/article/10.1088/0026-1394/54/1A/08008/meta DO - https://doi.org/10.1088/0026-1394/54/1A/08008 SN - 0026-1394 SN - 1681-7575 VL - 54 SP - Tech. Suppl. 2017, 08008, 1 EP - 47 PB - IOP Publishing CY - Bristol, UK AN - OPUS4-39394 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hsiao, I.-L. A1 - Bierkandt, Frank A1 - Reichardt, Ph. A1 - Luch, A. A1 - Huang, Y.-J. A1 - Jakubowski, Norbert A1 - Tentschert, J. A1 - Haase, A. T1 - Quantification and visualization of cellular uptake of TiO2 and Ag nanoparticles: comparison of different ICP-MS techniques N2 - Safety assessment of nanoparticles (NPs) requires techniques that are suitable to quantify tissue and cellular uptake of NPs. The most commonly applied techniques for this purpose are based on inductively coupled plasma mass spectrometry (ICP-MS). Here we apply and compare three different ICP-MS methods to investigate the cellular uptake of TiO2 (diameter 7 or 20 nm, respectively) and Ag (diameter 50 or 75 nm, respectively) NPs into differentiated mouse neuroblastoma cells (Neuro-2a cells). Cells were incubated with different amounts of the NPs. Thereafter they were either directly analyzed by laser ablation ICP-MS (LA-ICP-MS) or were lysed and lysates were analyzed by ICP-MS and by single particle ICP-MS (SP-ICP-MS). KW - Nanoparticles KW - Single particle ICP-MS KW - Laser ablation ICP-MS KW - Cellular internalization KW - Neurons PY - 2016 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-371620 DO - https://doi.org/10.1186/s12951-016-0203-z SN - 1477-3155 VL - 14 SP - Article 50 AN - OPUS4-37162 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Asadujjaman, Asad A1 - Kent, B. A1 - Bertin, Annabelle T1 - Phase transition and aggregation behaviour of an UCST-type copolymer poly(acrylamide-coacrylonitrile) in water: effect of acrylonitrile content, concentration in solution, copolymer chain length and presence of electrolyte N2 - An UCST-type copolymer of acrylamide (AAm) and acrylonitrile (AN) (poly(AAm-co-AN)) was prepared by reversible addition fragmentation chain transfer (RAFT) polymerization and its temperature-induced phase transition and aggregation behaviour studied by turbidimetry, static and dynamic light scattering, small angle neutron scattering (SANS) and cryo-transmission electron microscopy (cryo-TEM) measurements. The phase transition temperature was found to increase with increasing AN content in the copolymer, concentration of the solutions and copolymer chain length. A significant effect was observed onto the phase transition temperature by addition of different electrolytes into the copolymer solution. The copolymer chains were aggregated below the phase transition temperature and disaggregated above it. The size of the aggregates increases with increasing AN contents and concentration of the copolymer solutions below the phase transition temperature. The copolymer chains were expanded and weekly associated in solution above the phase transition temperature. A model is proposed to explain such association–aggregation behaviour of poly(AAm-co-AN) copolymers depending on AN contents and concentration of the copolymer solutions as a function of temperature. KW - Thermoresponsive polymers KW - UCST-type copolymer PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-394636 DO - https://doi.org/10.1039/c6sm02262f SN - 1744-683X SN - 1744-6848 VL - 13 IS - 3 SP - 658 EP - 669 PB - RSC AN - OPUS4-39463 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -