TY - JOUR A1 - Westwood, S. A1 - Martos, G. A1 - Josephs, R. A1 - Choteau, T. A1 - Wielgosz, R. A1 - Davies, S. A1 - Moawad, M. A1 - Tarrant, G. A1 - Chan, B. A1 - Alamgir, M. A1 - de Rego, E. A1 - Wollinger, W. A1 - Garrido, B. A1 - Fernandes, J. A1 - de Sena, R. A1 - Oliveira, R. A1 - Melanson, J. A1 - Bates, J. A1 - Mai Le, P. A1 - Meija, J. A1 - Quan, C. A1 - Huang, T. A1 - Zhang, W. A1 - Ma, R. A1 - Zhang, S. A1 - Hao, Y. A1 - He, Y. A1 - Song, S. A1 - Wang, H. A1 - Su, F. A1 - Zhang, T. A1 - Li, H. A1 - Lam, W. A1 - Wong, W. A1 - Fung, W. A1 - Philipp, Rosemarie A1 - Dorgerloh, Ute A1 - Meyer, Klas A1 - Piechotta, Christian A1 - Riedel, Juliane A1 - Westphalen, Tanja A1 - Giannikopoulou, P. A1 - Alexopoulos, Ch. A1 - Kakoulides, E. A1 - Kitamaki, Y. A1 - Yamazaki, T. A1 - Shimizu, Y. A1 - Kuroe, M. A1 - Numata, M. A1 - Pérez-Castorena, A. A1 - Balderas-Escamilla, M. A1 - Garcia-Escalante, J. A1 - Krylov, A. A1 - Mikheeva, A. A1 - Beliakov, M. A1 - Palagina, M. A1 - Tkachenko, I. A1 - Spirin, S. A1 - Smirnov, V. A1 - Tang Lin, T. A1 - Pui Sze, C. A1 - Juan, W. A1 - Lingkai, W. A1 - Ting, L. A1 - Quinde, L. A1 - Yizhao, C. A1 - Lay Peng, S. A1 - Fernandes-Whaley, M. A1 - Prevoo-Franzsen, D. A1 - Quinn, L. A1 - Nhlapo, N. A1 - Mkhize, D. A1 - Marajh, D. A1 - Chamane, S. A1 - Ahn, S. A1 - Choi, K. A1 - Lee, S. A1 - Han, J. A1 - Baek, S. A1 - Kim, B. A1 - Marbumrung, S. A1 - Jongmesuk, P. A1 - Shearman, K. A1 - Boonyakong, C. A1 - Bilsel, M. A1 - Gündüz, S. A1 - Ün, I. A1 - Yilmaz, H. A1 - Bilsel, G. A1 - Gökçen, T. A1 - Clarkson, C. A1 - Warren, J. A1 - Achtar, E. T1 - Mass fraction assignment of Bisphenol-A high purity material N2 - The CCQM-K148.a comparison was coordinated by the BIPM on behalf of the CCQM Organic Analysis Working Group for NMIs and DIs which provide measurement services in organic analysis under the CIPM MRA. It was undertaken as a "Track A" comparison within the OAWG strategic plan. CCQM-K148.a demonstrates capabilities for assigning the mass fraction content of a solid organic compound having moderate molecular complexity, where the compound has a molar mass in the range (75 - 500) g/mol and is non-polar (pKow < −2), when present as the primary organic component in a neat organic solid and where the mass fraction content of the primary component in the material is in excess of 950 mg/g. Participants were required to report the mass fraction of Bisphenol A present in one supplied unit of the comparison material. Participants using a mass balance method for the assignment were also required to report their assignments of the impurity components present in the material. Methods used by the seventeen participating NMIs or DIs were predominantly based on either stand-alone mass balance (summation of impurities) or qNMR approaches, or the combination of data obtained using both methods. The results obtained using thermal methods based on freezing-point depression methods were also reported by a limited number of participants. There was excellent agreement between assignments obtained using all three approaches to assign the BPA content. The assignment of the values for the mass fraction content of BPA consistent with the KCRV was achieved by most of the comparison participants with an associated relative standard uncertainty in the assigned value in the range (0.1 - 0.5)%. KW - Bisphenol-A KW - Purity assessment KW - Interlaboratory key comparison KW - Metrology PY - 2021 DO - https://doi.org/10.1088/0026-1394/58/1A/08015 VL - 58 IS - 1A SP - 08015 PB - IOP Publishing AN - OPUS4-54188 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nilsson, R. H. A1 - Taylor, A. F. S. A1 - Adams, R. I. A1 - Baschien, C. A1 - Bengtsson-Palme, J. A1 - Cangren, P. A1 - Coleine, C. A1 - Iršėnaitė, R. A1 - Martin-Sanchez, Pedro Maria A1 - Meyer, W. A1 - Oh, S.-Y. A1 - Sampaio, J. P. A1 - Seifert, K. A. A1 - Sklenář, F. A1 - Stubbe, D. A1 - Suh, S.-O. A1 - Summerbell, R. A1 - Svantesson, S. A1 - Unterseher, M. A1 - Visagie, C. M. A1 - Weiss, M. A1 - Woudenberg, J. HC. A1 - Wurzbacher, C. A1 - Van den Wyngaert, S. A1 - Yilmaz, N. A1 - Yurkov, A. A1 - Kõljalg, U. A1 - Abarenkov, K. A1 - Daniel, H.-M. A1 - Glassman, S. I. A1 - Hirooka, H. A1 - Irinyi, L. T1 - Taxonomic annotation of public fungal ITS sequences from the built environment – a report from an April 10–11, 2017 workshop (Aberdeen, UK) N2 - Recent DNA-based studies have shown that the built environment is surprisingly rich in fungi. These indoor fungi – whether transient visitors or more persistent residents – may hold clues to the rising levels of human allergies and other medical and building-related health problems observed globally. The taxo¬nomic identity of these fungi is crucial in such pursuits. Molecular identification of the built mycobiome is no trivial undertaking, however, given the large number of unidentified, misidentified, and technically compromised fungal sequences in public sequence databases. In addition, the sequence metadata required to make informed taxonomic decisions – such as country and host/substrate of collection – are often lacking even from reference and ex-type sequences. Here we report on a taxonomic annotation workshop (April 10–11, 2017) organized at the James Hutton Institute/University of Aberdeen (UK) to facilitate reproducible studies of the built mycobiome. The 32 participants went through public fungal ITS bar¬code sequences related to the built mycobiome for taxonomic and nomenclatural correctness, technical quality, and metadata availability. A total of 19,508 changes – including 4,783 name changes, 14,121 metadata annotations, and the removal of 99 technically compromised sequences – were implemented in the UNITE database for molecular identification of fungi (https://unite.ut.ee/) and shared with a range of other databases and downstream resources. Among the genera that saw the largest number of changes were Penicillium, Talaromyces, Cladosporium, Acremonium, and Alternaria, all of them of significant importance in both culture-based and culture-independent surveys of the built environment. KW - Indoor mycobiome KW - Built environment KW - Molecular identification KW - Fungi KW - Taxonomy KW - Systematics KW - Sequence annotation KW - Metadata KW - Open data PY - 2018 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-438949 DO - https://doi.org/10.3897/mycokeys.28.20887 SN - 1314-4049 SN - 1314-4057 VL - 28 SP - 65 EP - 82 PB - Pensoft Publishers CY - Washington, DC AN - OPUS4-43894 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Sieg, H. A1 - Braeuning, C. A1 - Kunz, B. M. A1 - Daher, H. A1 - Kästner, C. A1 - Krause, B.-C. A1 - Meyer, T. A1 - Jalili, P. A1 - Kogeveen, K. A1 - Böhmert, L. A1 - Lichtenstein, D. A1 - Burel, A. A1 - Chevance, S. A1 - Jungnickel, H. A1 - Tentschert, J. A1 - Laux, P. A1 - Braeuning, A. A1 - Gauffre, F. A1 - Fessard, V. A1 - Meijer, J. A1 - Estrela-Lopis, I. A1 - Thünemann, Andreas A1 - Luch, A. A1 - Lampen, A. T1 - Uptake and molecular impact of aluminum-containing nanomaterials on human intestinal caco-2 cells N2 - Aluminum (Al) is one of the most common elements in the earth crust and increasingly used in food, consumer products and packaging. Its hazard potential for humans is still not completely understood. Besides the metallic form, Al also exists as mineral, including the insoluble oxide, and in soluble ionic forms. Representatives of these three species, namely a metallic and an oxidic species of Al-containing nanoparticles and soluble aluminum chloride, were applied to human intestinal cell lines as models for the intestinal barrier. We characterized physicochemical particle parameters, protein corona composition, ion release and cellular uptake. Different in vitro assays were performed to determine potential effects and molecular modes of Action related to the individual chemical species. For a deeper insight into signaling processes, microarray transcriptome analyses followed by bioinformatic data analysis were employed. The particulate Al species showed different solubility in biological media. Metallic Al nanoparticles released more ions than Al2O3 nanoparticles, while AlCl3 showed a mixture of dissolved and agglomerated particulate entities in biological media. The protein corona composition differed between both nanoparticle species. Cellular uptake, investigated in transwell experiments, occurred predominantly in particulate form, whereas ionic Al was not taken up by intestinal cell lines. Transcellular transport was not observed. None of the Al species showed cytotoxic effects up to 200 mg Al/mL. The transcriptome analysis indicated mainly effects on oxidative stress pathways, xenobiotic metabolism and metal homeostasis. We have shown for the first time that intestinal cellular uptake of Al occurs preferably in the particle form, while toxicological effects appear to be ion-related. KW - Small-angle x-ray scattering KW - SAXS KW - Nanopatricle PY - 2018 DO - https://doi.org/10.1080/17435390.2018.1504999 SN - 1743-5390 VL - 12 IS - 9 SP - 992 EP - 1013 PB - Taylor & Francis AN - OPUS4-47432 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schneider, M. A1 - Drenkova-Tuhtan, A. A1 - Szczerba, Wojciech A1 - Gellermann, C. A1 - Meyer, C. A1 - Steinmetz, H. A1 - Mandel, K. A1 - Sextl, G. T1 - Nanostructured ZnFeZr oxyhydroxide precipitate as efficient phosphate adsorber in waste water: understanding the role of different material-building-blocks N2 - In the recent years great effort has been made to find materials and technologies for removing and recycling phosphate from waste water. We herein present the detailed study on a nanostructured multicomponent material, which turned out to be a very efficient phosphate adsorber. The role of each constituent is carefully examined to understand the collaborative interaction of the components of the nanostructured adsorber. We found evidence that it is particularly the nanostructure of this material, which has a crucial influence on the phosphate Adsorption performance, indicating a synergetic effect of the different components. Moreover, the adsorption mechanism was studied dependent on the concentration of phosphate, changing from a Freundlich/Langmuir-like behaviour to a BET-like multilayer adsorption of phosphate on the material. Our work demonstrates that there is high potential for discovering new adsorber materials for environmental applications through careful engineering of the chemical composition in close connection with the materials (nano) structure. KW - Adsober KW - Phosphate adsorption KW - Waste water treatment PY - 2017 DO - https://doi.org/10.1039/c6en00507a SN - 2051-8153 SN - 2051-8161 VL - 4 IS - 1 SP - 180 EP - 190 PB - RSC AN - OPUS4-39700 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Fischer, C. A1 - Wu, J. A1 - Meyer, U. A1 - Kong, B. A1 - Schmidt, Martin A1 - Wuttke, M. A1 - Drebenstedt, C. A1 - Barth, Uli A1 - Rüter, H. T1 - Eight years of successful bilateral cooperation: Milestones of sino-german research T2 - 2nd International conference on coal fire research (ICCFR2) CY - Berlin, Germany DA - 2010-05-19 KW - Underground coal fires KW - Sino-german cooperation PY - 2010 SN - 978-3-86012-397-3 IS - Introduction SP - 3 EP - 18 AN - OPUS4-21460 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Knabe, C. A1 - Berger, Georg A1 - Gildenhaar, Renate A1 - Meyer, J. A1 - Howlett, C. A1 - Markovic, B. A1 - Zreiqat, H. T1 - Effect of rapidly resorbable calcium phosphates and a calcium phosphate bone cement on the expression of bone-related genes and proteins in vitro N2 - The use of biodegradable bone substitutes is advantageous for alveolar ridge augmentation because it avoids second-site surgery for autograft harvesting. This study examines the effect of novel, rapidly resorbable calcium phosphates and a calcium phosphate bone cement on the expression of bone-related genes and proteins by human bone-derived cells (HBDCs) and compares this behavior to that of tricalciumphosphate (TCP). Test materials were -TCP, two materials with a crystalline phase Ca2KNa(PO4)2 and with a small amorphous portion containing either magnesium potassium phosphate (material denominated GB14) or silica phosphate (material denominated GB9), and a calcium phosphate bone cement (material denominated Biocement D). HBDCs were grown on the substrata for 3, 7, 14, and 21 days, counted, and probed for various mRNAs and proteins (type I collagen, osteocalcin, osteopontin, osteonectin, alkaline phosphatase, and bone sialoprotein). All substrates supported continuous cellular growth for 21 days. In the presence of GB14 and Biocement D specimens cell proliferation was reduced and cell differentiation increased. At day 21, the greatest number of cells was found on GB9 expressing significantly higher levels of bone-related proteins than cells grown on all other surfaces. Because all novel materials facilitated the expression of the osteoblastic phenotype at least as much as TCP and the polystyrene control, these biomaterials can be regarded as excellent candidate bone substitute materials. GB9 induced the highest proliferation and cellular differentiation after 21 days of incubation, suggesting that this material may possess a higher potency for enhancing osteogenesis than TCP. © 2004 Wiley Periodicals, Inc. J Biomed Mater Res 69A: 145-154, 2004 KW - Calcium phosphate ceramics KW - Human bone-derived cells KW - Cell-biomaterial interactions KW - Calcium phosphate cements KW - In situ hybridization PY - 2004 DO - https://doi.org/10.1002/jbm.a.20131 SN - 1549-3296 SN - 1552-4965 VL - 69 IS - 1 SP - 145 EP - 154 PB - Wiley CY - Hoboken, NJ AN - OPUS4-3502 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Fischer, C. A1 - Schmidt, Martin A1 - Meyer, U. A1 - Barth, Uli A1 - Drebenstedt, C. A1 - Wuttke, M. W. T1 - Innovative Technologien für die Erkundung, Löschung und Beobachtung von Kohlebränden - Phase B - N2 - Aufbauend auf den Erkenntnissen der Phase A, die sich auf das grundlegende Verständnis von Kohlebränden, sowie der Voraussetzung und des prinzipiellen Ablaufs der physikalischchemischen Brandprozesse konzentriert haben, erfolgte in Phase B eine Fokussierung auf Methoden zur Vermeidung von Kohlebränden, sowie der Löschung und Überwachung von Kohlebrandzonen, um einen Beitrag zur Verminderung von C02-Emissionen und zum Erhalt der nutzbaren Energieressourcen leisten zu können. Diese Arbeiten erfolgten insbesondere mit Bezug zu den „Clean Development Mechanisms“ (CDM), die im Rahmen des Kyoto-Protokolls entwickelt worden sind. Eine Zertifizierung von Löschaktivitäten im Rahmen des Kyoto-Protokolls setzt dabei eine nachvollziehbare Ermittlung der kohlebrandbezogenen C02-Emissionen und eine belastbare Abschätzung der durch die Löschung verringerten Emissionsmengen voraus. Wesentliche Arbeiten konzentrierten sich auf die Entwicklung von Verfahren, die eine solche Abschätzung gewährleisten können. Dazu wurden unterschiedliche Ansätze entwickelt und anhand der erhobenen Felddaten überprüft. Die untersuchten Ansätze konzentrierten sich dabei auf Verfahren, die eine Ermittlung des vorhandenen Kohlevolumens, die Erfassung der emittierten Gase und die durch die Kohlebrände verursachten Temperaturanomalien an der Tagesoberfläche ermöglichen. Die direkten Arbeiten zum Thema CDM wurden dabei in einem Arbeitspaket unter Federführung der BGR gebündelt. Die deutsche Initiative zur Erforschung der Kohlenbrände in der V.R. China leistete zweifelsfrei signifikante Beiträge zu den oben genannten Zielen. Durch die inventiven Ansätze im Bereich der Brandbewältigung konnte darüber hinaus auch in Teilen die ökonomischen Chancen für ein Engagement deutscher Unternehmen aufgezeigt werden. KW - Kohlebrände KW - Brandbekämpfung KW - Branderkundung PY - 2011 DO - https://doi.org/10.2314/GBV:664529690 SP - 1 EP - 39 AN - OPUS4-25013 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Bresch, Harald A1 - Meyer-Plath, Asmus A1 - Burgdorf, T. A1 - Packroff, R. A1 - Apel, P. A1 - Adolf, P. A1 - Jesse, A. A1 - Leuschner, C. A1 - Bosse, H. A1 - Dubbert, W. A1 - Epp, A. A1 - Gebel, T. A1 - Götz, M. A1 - Herzberg, F. A1 - Hornbogen, T. A1 - Kersten, N. A1 - Kneuer, C. A1 - Kujath, P. A1 - Pipke, R. A1 - Plitzko, s. A1 - Schlesier, K. A1 - Schröder, F. A1 - Schwirn, K. A1 - Sommer, Y. A1 - Tentschert, J. A1 - Völker, D. A1 - Wolf, T. T1 - 1. Bilanz zur gemeinsamen Forschungsstrategie der Ressortforschungseinrichtungen des Bundes 'Nanotechnologie - Gesundheits- und Umweltrisiken von Nanomaterialien' (2007 - 2011) KW - Nanotechnologie KW - Nanopartikel KW - Nanomaterial KW - Bundesoberbehörden KW - Forschungsstrategie PY - 2013 SP - 1 EP - 124 CY - Berlin AN - OPUS4-28538 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hennig, C. A1 - Takao, S. A1 - Takao, K. A1 - Weiss, s. A1 - Kraus, Werner A1 - Emmerling, Franziska A1 - Meyer, M. A1 - Scheinost, A.C. T1 - Identification of hexanuclear actinide(IV) carboxylates with thorium, uranium and neptunium by EXAFS spectroscopy N2 - Hydrated actinide(IV) ions undergo hydrolysis and further polymerization and precipitation with increasing pH. The resulting amorphous and partly crystalline oxydydroxides AnOn(OH)4-2n·xH2O can usually be observed as colloids above the An(IV) solubility limit. The aging process of such colloids results in crystalline AnO2. The presence of carboxylates in the solution prevents the occurrence of such colloids by formation of polynuclear complexes through a competing reaction between hydrolysis and ligation. The majority of recently described carboxylates reveals a hexanuclear core of [An6(µ3-O)4(µ3-OH)4]12+ terminated by 12 carboxylate ligands. We found that the An(IV) carboxylate solution species remain often preserved in crystalline state. The An(IV) carboxylates show An–An distances which are ~ 0.03 Å shorter than the An–An distances in AnO2 like colloids. The difference in the distances could be used to identify such species in solution. T2 - XAFS15 - 15th International conference on X-ray absorption fine structure CY - Beijing, China DA - 22.07.2012 KW - Carboxylates KW - EXAFS KW - Actinide PY - 2013 DO - https://doi.org/10.1088/1742-6596/430/1/012116 SN - 1742-6588 SN - 1742-6596 VL - 430 SP - 012116-1 EP - 012116-5 PB - IOP Publ. CY - Bristol, UK AN - OPUS4-28525 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lichtenstein, D. A1 - Ebmeyer, J. A1 - Meyer, T. A1 - Behr, A.-C. A1 - Kästner, Claudia A1 - Böhmert, L. A1 - Juling, J. A1 - Niemann, B. A1 - Fahrenson, C. A1 - Selve, S. A1 - Thünemann, Andreas A1 - Meijer, J. A1 - Estrela-Lopis, I. A1 - Bräuning, A. A1 - Lampen, A. T1 - It takes more than a coating to get nanoparticles through the intestinal barrier in vitro N2 - Size and shape are crucial parameters which have impact on the potential of nanoparticles to penetrate cell membranes and epithelial barriers. Current research in nanotoxicology additionally focuses on particle coating. To distinguish between core- and coating-related effects in nanoparticle uptake and translocation, two nanoparticles equal in size, coating and charge but different in core material were investigated. Silver and iron oxide nanoparticles coated with poly(acrylic acid) were chosen and extensively characterized by small-angle x-ray scattering, nanoparticle tracing analysis and transmission electron microscopy (TEM). Uptake and transport were studied in the intestinal Caco-2 model in a Transwell System with subsequent elemental analysis. TEM and ion beam microscopy were conducted for particle visualization. Although equal in size, charge and coating, the behavior of the two particles in Caco-2 cells was different: while the internalized amount was comparable, only iron oxide nanoparticles additionally passed the epithelium. Our findings suggest that the coating material influenced only the uptake of the nanoparticles whereas the translocation was determined by the core material. Knowledge about the different roles of the particle coating and core materials in crossing biological barriers will facilitate toxicological risk assessment of nanoparticles and contribute to the optimization of pharmacokinetic properties of nano-scaled pharmaceuticals. KW - Silver KW - Nanoparticle KW - Polymer KW - Polyacrylic acid PY - 2017 DO - https://doi.org/10.1016/j.ejpb.2016.12.004 SN - 0939-6411 SN - 1873-3441 VL - 118 SP - 21 EP - 29 PB - Elsevier AN - OPUS4-41170 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Scheuerlein, C. A1 - Andrieux, J. A1 - Michels, M. A1 - Lackner, F. A1 - Chiriac, R. A1 - Hagner, M. A1 - Di Michiel, M. A1 - Meyer, Christian A1 - Toche, F. ED - Foley, C. P. T1 - Effect of the fabrication route on the phase and volume changes during the reaction heat treatment of Nb3Sn superconducting wires N2 - Accelerator magnets that can reach magnetic fields well beyond the Nb-Ti performance limits are presently being built and developed, using Nb3Sn superconductors. This technology requires reaction heat treatment (RHT) of the magnet coils, during which Nb3Sn is formed from its ductile precursor materials (a “wind and react” approach). The Nb3Sn microstructure and microchemistry are strongly influenced by the conductor fabrication route, and by the Phase changes during RHT. By combining in situ differential scanning calorimetry, high Energy synchrotron x-ray diffraction, and micro-tomography experiments, we have acquired a unique data set that describes in great detail the phase and microstructure changes that take place during the processing of restacked rod process (RRP), powder-in-tube (PIT), and internal tin (IT) Nb3Sn wires. At temperatures below 450 ° the phase evolutions in the three wire types are similar, with respectively solid state interdiffusion of Cu and Sn, Cu6Sn5 formation, and Cu6Sn5 peritectic transformation. Distinct differences in phase evolutions in the wires are found when temperatures exceed 450 °C. The volume changes of the conductor during RHT are a difficulty in the production of Nb3Sn accelerator magnets. We compare the wire diameter changes measured in situ by dilatometry with the phase and void volume evolution of the three types of Nb3Sn wire. Unlike the Nb3Sn wire length changes, the wire diameter evolution is characteristic for each Nb3Sn wire type. The strongest volume increase, of about 5%, is observed in the RRP wire, where the main diameter increase occurs above 600 °C upon Nb3Sn formation. KW - Nb3Sn KW - Microstructure KW - Phase transformations KW - Volume changes KW - X-ray diffraction KW - Differential scanning calorimetry KW - Synchrotron micro-tomography PY - 2020 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-505128 DO - https://doi.org/10.1088/1361-6668/ab627c VL - 33 IS - 3 SP - 034004 PB - IOP Publishing CY - Bristol (UK) AN - OPUS4-50512 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zientek, Nicolai A1 - Laurain, C. A1 - Meyer, Klas A1 - Paul, Andrea A1 - Engel, D. A1 - Guthausen, G. A1 - Kraume, M. A1 - Maiwald, Michael T1 - Automated data evaluation and modelling of simultaneous F-19-H-1 medium-resolution NMR spectra for online reaction monitoring N2 - Medium-resolution nuclear magnetic resonance spectroscopy (MR-NMR) currently develops to an important analytical tool for both quality control and processmonitoring. In contrast to high-resolution onlineNMR (HR-NMR),MR-NMRcan be operated under rough environmental conditions. A continuous re-circulating stream of reaction mixture fromthe reaction vessel to the NMR spectrometer enables a non-invasive, volume integrating online analysis of reactants and products. Here, we investigate the esterification of 2,2,2-trifluoroethanol with acetic acid to 2,2,2-trifluoroethyl acetate both by 1H HR-NMR (500MHz) and 1H and 19F MRNMR (43MHz) as amodel system. The parallel online measurement is realised by splitting the flow,which allows the adjustment of quantitative and independent flow rates, both in the HR-NMR probe as well as in the MR-NMR probe, in addition to a fast bypass line back to the reactor. One of the fundamental acceptance criteria for online MR-MNR spectroscopy is a robust data treatment and evaluation strategy with the potential for automation. The MR-NMR spectra are treated by an automated baseline and phase correction using the minimum entropy method. The evaluation strategies comprise (i) direct integration, (ii) automated line fitting, (iii) indirect hard modelling (IHM) and (iv) partial least squares regression (PLS-R). To assess the potential of these evaluation strategies for MR-NMR, prediction results are compared with the line fitting data derived from the quantitative HR-NMR spectroscopy. Although, superior results are obtained from both IHM and PLS-R for 1H MR-NMR, especially the latter demands for elaborate data pretreatment, whereas IHM models needed no previous alignment. KW - NMR KW - 1H-NMR KW - 19F-NMR KW - Medium-resolution NMR KW - Online NMR KW - Quantitative NMR KW - Reaction monitoring KW - Data processing KW - Automation KW - Process analytical technology KW - IHM KW - Indirect hard modeling KW - Chemometrics KW - PLS-R KW - Partial least squares regression PY - 2016 UR - http://onlinelibrary.wiley.com/doi/10.1002/mrc.4216/abstract DO - https://doi.org/doi:10.1002/mrc.4216 VL - 54 SP - 513 EP - 520 PB - John Wiley & Sons, Ltd CY - Hoboken, New Jersey, USA AN - OPUS4-36135 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Kern, Simon A1 - Wander, Lukas A1 - Meyer, Klas A1 - Guhl, Svetlana A1 - Gottu Mukkula, A. R. A1 - Holtkamp, M. A1 - Salge, M. A1 - Fleischer, C. A1 - Weber, N. A1 - Engell, S. A1 - Paul, Andrea A1 - King, R. A1 - Maiwald, Michael T1 - Raw data of pilot plant runs for CONSENS project (Case study 1) N2 - In case study one of the CONSENS project, two aromatic substances were coupled by a lithiation reaction, which is a prominent example in pharmaceutical industry. The two aromatic reactants (Aniline and o-FNB) were mixed with Lithium-base (LiHMDS) in a continuous modular plant to produce the desired product (Li-NDPA) and a salt (LiF). The salt precipitates which leads to the formation of particles. The feed streams were subject to variation to drive the plant to its optimum. The uploaded data comprises the results from four days during continuous plant operation time. Each day is denoted from day 1-4 and represents the dates 2017-09-26, 2017-09-28, 2017-10-10, 2017-10-17. In the following the contents of the files are explained. KW - Process Analytical Technology KW - Multivariate Data Analysis KW - Nuclear Magnetic Resonance KW - Near Infrared Spectroscopy KW - Continuous Manufacturing KW - CONSENS PY - 2018 DO - https://doi.org/10.5281/zenodo.1438233 PB - Zenodo CY - Geneva AN - OPUS4-48063 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Meyer, S. A1 - Richter, S. A1 - Balski, Matthias A1 - Hagendorf, C. ED - Thirsk, M. T1 - Trace element analysis in crystalline silicon N2 - The reliable analysis of trace elements in silicon is of fundamental importance for the understanding of material properties and quality control of solar cells. This paper presents a demonstration of the power of two analytical techniques for the determination of trace elements in solar silicon: inductively coupled plasma mass spectrometry (ICP-MS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS). These techniques are among the few that achieve sufficiently low detection limits and they may complement each other because of their specific performance. Examples are given of the quantitative chemical analysis of boron, phosphorus and iron in different types of solar silicon, as well as of the enrichment of metals and alkali metals in Si3N4 precipitates. PY - 2013 SN - 978-0-9565331-3-5 SP - 34 EP - 38 PB - Photovoltaics International CY - London, UK AN - OPUS4-29823 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meyer, S. A1 - Timmel, S. A1 - Gläser, M. A1 - Braun, Ulrike A1 - Wachtendorf, Volker A1 - Hagendorf, C. T1 - Polymer foil additives trigger the formation of snail trails in photovoltaic modules N2 - After several months of operation, many photovoltaic (PV) modules develop a discolouration defect called snail trails which appear as irregular dark traces across the cells. These traces are caused by silver nanoparticles accumulating within the encapsulation foil directly above the grid finger. In this work we systematically investigate combinations of encapsulation and back-sheet foils with respect to their susceptibility for snail trails. We can show that certain additive compositions within the encapsulation and back sheet foils are critical for the formation of the discolouring silver nanoparticles. We suggest a reaction model explaining the formation of snail trails from a chemical point of view. This fundamental understanding allows the rapid testing of foils for their snail trail sensitivity as well as the special design of resistant foils. KW - Snail trails KW - Encapsulation foil KW - Back-sheet foil KW - Additives KW - Silver nanoparticles PY - 2014 DO - https://doi.org/10.1016/j.solmat.2014.06.028 SN - 0927-0248 VL - 130 SP - 64 EP - 70 PB - Elsevier B.V. CY - Amsterdam [u.a.] AN - OPUS4-31249 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meyer, S. A1 - Timmel, S. A1 - Richter, S. A1 - Werner, M. A1 - Gläser, M. A1 - Swatek, S. A1 - Braun, Ulrike A1 - Hagendorf, C. T1 - Silver nanoparticles cause snail trails in photovoltaic modules N2 - After some months of operation, a number of PV modules develop a discolouration defect called 'snail trails', or 'snail traces', which appear as irregular dark stripes across the cells. Whereas these traces were soon identified as discoloured silver contacts along the cell edges or at micro cracks, the chemical and mechanistic reasons for this phenomenon have not yet been resolved in detail. In this work we show that silver nanoparticles accumulating within the encapsulation foil cause the brownish discolouration, and that certain additives of encapsulation and back sheet foils trigger the formation of these nanoparticles. KW - Snail trails KW - Cell cracks KW - Encapsulation foil KW - Ag contact finger KW - Nanoparticles PY - 2014 DO - https://doi.org/10.1016/j.solmat.2013.11.013 SN - 0927-0248 VL - 121 SP - 171 EP - 175 PB - Elsevier B.V. CY - Amsterdam [u.a.] AN - OPUS4-30059 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Paul, Astrid A1 - Ziegert, C. A1 - Fontana, Patrick A1 - Meyer, J. T1 - StandardBoard - Produktnorm für Lehmplatten T1 - StandardBoard - A product standard for earthen panels N2 - Die Anwendung von modernen Lehmbaustoffen hat in den letzten Jahren überdurchschnittliche Wachstumsraten erreicht. Für Bauherren und Planer ausschlaggebend ist häufig ihr extrem niedriger CO2-Äquivalentkennwert. Entsprechend wurden Lehmplatten in einem Projekt mit Pilotcharakter für den Umbau des alten Abgeordnetenhauses in Bonn zum Gebäude des Klimareferats der Vereinten Nationen verwendet. Bei der Entscheidung für die Bauweise mit Lehmplatten standen vor allem raumklimatische und schallschutztechnische, das heißt gesundheitliche Aspekte, aber auch der Wunsch nach erhöhter Nachhaltigkeit im Vordergrund. Durch das Fehlen einer Norm entstehen im Vergleich zu geregelten Bauprodukten jedoch noch deutliche Wettbewerbsnachteile für Produzenten von Lehmplatten. Planer und Anwender sehen aufgrund fehlender Prüfzertifikate nicht selten von der Anwendung dieser Lehmbaustoffe ab. Wie schon für Lehmsteine und Lehmmörtel sollen deshalb jetzt auch für Lehmplatten an der Bundesanstalt für Materialforschung und -prüfung (BAM) in dem Projekt StandardBoard Grundlagen für eine Produktnorm geschaffen werden. Darin ist als Projektpartner der Hersteller Conluto beteiligt. Zweck des in Erarbeitung befindlichen Regelwerks ist es, über die Festlegung von Qualitätsanforderungen und Prüfvorschriften die Gebrauchstauglichkeit von Lehmplatten sicherzustellen und somit einerseits Sicherheit für Planer und Anwender und andererseits Vergleichbarkeit und damit Konkurrenzfähigkeit zu konventionellen Plattenprodukten für gleiche Einbaubereiche zu erreichen. Darüber hinaus stellt sie ein Instrument dar, um die besonderen ökologischen und bauphysikalischen Eigenschaften der Lehmbaustoffe hervorzuheben. Die Erarbeitung des Regelwerks erfolgt in enger Abstimmung mit dem Dachverband Lehm e. V. (DVL). N2 - In recent years. the utilization of modern building materials made from soil has extended considerably. For building principals and designers. this decision is often determined by their extremely low carbon dioxide equivalent. A paradigm is the application of earth panels in the conversion of the former House of Representatives in Bonn to the secretariat of the United Nations Framework Convention on Climate Change. The choice of earth panels was determined not only by considerations of indoor climate and acoustic insulation issues. but particularly by an endeavour to attain a high level of sustainability. The lack of a standard causes producers of earth panels to experience considerable competitive disadvantages. With the absence of test certificates. designers as well as implementers refrain from using earth materials. The project StandardBoard has been initiated with the purpose of developing the basis for a product standard for earth panels. being realized at the BAM. where also standards for earth blocks and earth mortars have been developed. The BAM is cooperating with the project partner Conluto. a manufacturer of earth panels. The object of the standard being in development is to guarantee the usability of earth panels by stating quality requirements and testing procedures and thereby to achieve safety for designers and users as well as competitiveness with established panels. Furthermore. a standard allows to emphasize the special ecological and climatic features of earth materials. The drafting of the standard is coordinated in close relation to the German Association for Earth Construction (DVL). T2 - Lehm 2016 - 7. Internationale Fachtagung für Lehmbau - 7th International Conference on Building with Earth CY - Weimar, Germany DA - 12.11.2016 KW - Baustoffe KW - Moderne Lehmbaustoffe KW - Lehmplatte KW - Normung KW - Prüfung KW - Produktqualität KW - Building materials KW - Modern earthen building materials KW - Earth panel KW - Standardisation KW - Testing KW - Product quality PY - 2016 SP - 1 EP - 12 PB - Eigenverlag Dachverband Lehm e. V. CY - Weimar AN - OPUS4-38996 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Bresch, Harald A1 - Lexow, Jürgen A1 - Sturm, Heinz A1 - Packroff, R. A1 - Völker, D. A1 - Mutz, D. A1 - Bosse, H. A1 - Gebel, T. A1 - Pipke, R. A1 - Marx, R. A1 - Plitzko, S. A1 - Niesmann, K. A1 - Meyer-Plath, A. A1 - Burgdorf, T. A1 - Engel, N. A1 - Epp, A. A1 - Haase, A. A1 - Herzberg, F. A1 - Laux, P. A1 - Oberemm, A. A1 - Sommer, Y. A1 - Tentschert, J. A1 - Ulm, G. A1 - Schwirn, K. A1 - Liesegang, C. T1 - Nanomaterialien und andere innovative Werkstoffe: anwendungssicher und umweltverträglich T1 - Nanomaterials and other advanced materials: application safety and environmental compatibility N2 - Mit einer langfristigen Forschungsstrategie begleiten die für die Sicherheit von Mensch und Umwelt zuständigen Bundesoberbehörden (Umweltbundesamt, Bundesinstitut für Risikobe-wertung, Bundesanstalt für Arbeitsschutz und Arbeitsmedizin, Bundesanstalt für Materialfor-schung und -prüfung und Physikalisch-Technische Bundesanstalt) die rasch voranschreiten-de Entwicklung neuer Materialien unter den Gesichtspunkten des Arbeits-, Verbraucher- und Umweltschutzes. Die Strategie steht daher in enger Verbindung zu den öffentlichen Förder-programmen für Nanomaterialien und andere innovative Werkstoffe, z. B. des BMBF („Vom Material zur Innovation“) und der EU („Horizon 2020“). Die Forschungsstrategie baut auf den bisherigen Ergebnissen der 2008 begonnenen und 2013 erstmals bilanzierten gemeinsamen Forschungsstrategie der Bundesoberbehörden „Nanotechnologie - Gesundheits- und Umweltrisiken von Nanomaterialien"1 auf und erweitert den Blickwinkel auch auf andere Materialinnovationen, bei denen vergleichbare Risiken für Mensch und Umwelt bestehen oder abgeklärt werden müssen. Darüber hinaus greift sie die Idee „anwendungssichere chemische Produkte“2 aus der Initiative „Neue Qualität der Arbeit“ (INQA) des Bundesministeriums für Arbeit und Soziales (BMAS) und das Konzept der nach-haltigen Chemie3 auf, das vom Bundesministerium für Umwelt, Naturschutz, Bau und Reak-torsicherheit (BMUB) unterstützt wird. Durch eine anwendungssichere und umweltverträgli-che Gestaltung innovativer Materialien und ihrer Folgeprodukte sollen nicht akzeptable Risi-ken für Mensch und Umwelt von Anfang an weitgehend ausgeschlossen werden. Dies kann erreicht werden durch 1. die Verwendung sicherer Materialien ohne Gefahreneigenschaften für Mensch und Umwelt (direkte Anwendungssicherheit) oder 2. eine Produktgestaltung, die über den gesamten Lebenszyklus emissionsarm und umweltverträglich ist (integrierte Anwendungssicherheit) oder 3. eine Unterstützung des Anwenders (product stewardship) durch den Hersteller bei technischen, organisatorischen und persönlichen Schutzmaßnahmen zur sicheren Verwendung und Entsorgung des Produktes (unterstützte Anwendungssicherheit). Die Fortschreibung der Forschungsstrategie soll als Bestandteil des Nanoaktionsplans 2020 der Bundesregierung Beiträge der Ressortforschung zu folgenden Schwerpunkten leisten: • Charakterisierung und Bewertung der Risiken von Materialinnovationen • Unterstützung von Forschungseinrichtungen und Unternehmen • Fortschreiben von Rechtsvorschriften und Praxisempfehlungen 1 http://www.baua.de/nn_47716/de/Themen-von-A-Z/Gefahrstoffe/Nanotechnologie/pdf/Forschungsstrategie.pdf 2 http://www.baua.de/de/Themen-von-A-Z/Gefahrstoffe/Nachhaltige-Chemie/Nachhaltige-Chemie.html 3 http://www.umweltbundesamt.de/themen/chemikalien/chemikalien-management/nachhaltige-chemie 2 • Gesellschaftliche Akzeptanz Die Forschungsstrategie soll mit Projekten und anderen forschungsnahen Aktivitäten umge-setzt werden. Dies umfasst die eigene Forschung der Häuser, die extramurale Ausschrei-bung und Vergabe von Forschungsdienstleistungen sowie die Beteiligung an vorwiegend öffentlich geförderten Drittmittelprojekten. Hinzu kommen Aktivitäten im Rahmen der Politik-beratung und der hoheitlichen Aufgaben. Mit inter- und transdisziplinären Ansätzen soll die Risiko- und Sicherheitsforschung enger mit der Innovationsforschung und Materialentwick-lung verknüpft werden. Die Forschungsstrategie ist aufgrund der raschen Entwicklungen auf diesem Gebiet für den Zeitraum bis 2020 angelegt. Die Forschungsziele adressieren die in diesem Zeitraum voraussichtlich umsetzbaren Forschungsansätze. Die Forschungsstrategie wird durch einen Arbeitskreis begleitet und spätestens mit Ablauf des Nanoaktionsplans 2020 evaluiert und angepasst. KW - Forschungsstrategie KW - Bundesoberbehörden KW - Nanomaterialien KW - Innovative Werkstoffe KW - Nano PY - 2016 UR - https://www.bam.de/_SharedDocs/DE/Downloads/nano-forschungsstrategie-2016.pdf?__blob=publicationFile&v=3 UR - http://www.baua.de/de/Themen-von-A-Z/Gefahrstoffe/Nanotechnologie/pdf/Fortschreibung-Forschungsstrategie.pdf?__blob=publicationFile&v=3 UR - http://www.bmub.bund.de/fileadmin/Daten_BMU/Download_PDF/Nanotechnologie/forschungsstrategie_bundesoberbehoerden_de_bf.pdf SP - 1 EP - 28 PB - UBA/BfR/BAuA/BAM/PTB CY - Berlin AN - OPUS4-37526 LA - mul AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rosemann, Paul A1 - Müller, C. A1 - Meyer, A. A1 - Halle, T. ED - Lampke, T. ED - Wagner, G. ED - Wagner, M. F.-X. T1 - Einfluss von Stickstoff auf Mikrostruktur und Korrosionsverhalten martensitischer nichtrostender Stähle N2 - Die Korrosionsbeständigkeit martensitischer nichtrostender Stähle (MNS) wird wesentlich von der chemischen Zusammensetzung und dem Wärmebehandlungszustand beeinflusst. Beides bestimmt die Verteilung der Legierungselemente im Gefüge und die daraus resultierenden Werkstoffeigenschaften. Das Legieren mit Stickstoff bewirkt im Allgemeinen eine Verbesserung der Lochkorrosionsbeständigkeit von nichtrostenden Stählen. Bei martensitischen nichtrostenden Stählen ist dieser Effekt nicht nur auf den Stickstoffgehalt selbst zurückzuführen, sondern auch auf den gleichzeitig verringerten Kohlenstoffgehalt, der ebenfalls das Ergebnis der Wärmebehandlung beeinflusst. In dieser Arbeit wird der Einfluss von Stickstoff auf die Korrosionsbeständigkeit in Bezug zum Härtungsprozess von MNS dargestellt. Dazu wird vergleichend der Effekt von Austenitisierungsdauer, -temperatur und Abkühlgeschwindigkeit auf Gefüge, Härte und Korrosionsbeständigkeit der MNS X50CrMoV15 und X30CrMoN15 1 untersucht. Die Abkühlgeschwindigkeit wurde mit dem Stirnabschreckversuch gezielt variiert, um den Einfluss von Abkühlgeschwindigkeiten von > 100 K/s bis 1 K/s zu charakterisieren. Die Veränderungen der Korrosionsbeständigkeit werden durch die elektrochemisch potentiodynamische Reaktivierung (EPR) und durch die Bestimmung kritischer Lochkorrosionspotentiale dokumentiert. Neben diesem experimentellen Ansatz werden auch die Ergebnisse von thermodynamischen Berechnungen mit der Software Thermocalc vorgestellt und abschließend auch zur Interpretation des Einflusses von Stickstoff auf die Korrosionsbeständigkeit martensitischer nichtrostender Stähle genutzt. T2 - 18. Werkstofftechnisches Kolloquium der TU Chemnitz CY - Chemnitz, Germany DA - 10.03.2016 KW - Korrosionsbeständigkeit KW - Corrosion resistance KW - Wärmebehandlung KW - Heat treatment KW - Nichtrostende Stähle KW - Stainless steels KW - Thermocalc KW - Thermocalc PY - 2016 SN - 978-3-00-052212-3 SN - 1439-1597 VL - 59 SP - 325 EP - 336 PB - TU Chemnitz, Fakultät für Maschinenbau, Institut für Werkstoffwissenschaft und Werkstofftechnik CY - Chemnitz AN - OPUS4-37263 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Labarraque, G. A1 - Oster, C. A1 - Fisicaro, P. A1 - Meyer, Christian A1 - Vogl, Jochen A1 - Noordmann, J. A1 - Rienitz, O. A1 - Riccobono, F. A1 - Donet, S. T1 - Reference measurement procedures for the quatification of platinum-group elements (PGEs) from automotive exhaust emissions N2 - The major source of the anthropogenic platinum group element (PGE) emission is attributed to the use of catalytic converters in automobiles. This paper describes the work performed by three National Metrology Institutes (Laboratoire national de métrologie et d’essais, by the Physikalisch-technische bundesanstalt, Bundesanatalt für materialforschung und prûfung), in the framework of the Joint Research Project 'PartEmission' under the European Metrology Research Program. An analytical procedure based on a cationic exchange protocol and the isotope dilution or standard addition using an Inductived Coupled Plasma Mass Spectrometer, ICP-MS, for the quantification of the elements Pt, Pd and Rh from automotive exhaust emissions is described. Results obtained on a road dust certified reference (BCR 723) material showed a good agreement with the certified values, at ng/g levels, and relative expanded uncertainties within the range of 7–10%. Analysis of filters impacted with automotive exhaust particle emissions (from a diesel engine) showed the amount of collected PGE at levels of 10–1000 pg/filter. Their quantifications followed the developed analytical protocol that had been carried out with relative expanded uncertainties in the range of a few per cent up to 20% per filter. Nevertheless, a lack of homogeneity between the filters was observed, making the comparison between the project partners difficult in the sake of the validation of their analytical procedures on real samples. KW - Automotive pollution KW - Catalytic converters KW - Platinum group elements (PGE) KW - ICP-MS KW - Isobaric interferences KW - Cationic exchange KW - Reference measurement procedures KW - Double isotope dilution KW - Palladium KW - Platinum KW - Automotive exhaust emissions KW - IDMS PY - 2015 DO - https://doi.org/10.1080/03067319.2015.1058931 SN - 0306-7319 SN - 1029-0397 SN - 0092-9085 VL - 95 IS - 9 SP - 777 EP - 789 PB - Gordon and Breach CY - New York, NY AN - OPUS4-34015 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -