TY - CONF A1 - van der Kolk, G. J. A1 - Hurkmans, A. A1 - Trinh, T. A1 - Fleischer, W. A1 - Beck, Uwe A1 - Griepentrog, Michael T1 - Coating evaluation of decorative PVD finishes T2 - 41st Annual Technical Conference CY - Boston, MA, USA DA - 1998-04-18 PY - 1998 UR - http://www.knovel.com/web/portal/browse/display?_EXT_KNOVEL_DISPLAY_bookid=272 SN - 1-591-24158-8 SP - 44 EP - 45 PB - Society of Vacuum Coaters CY - Albuquerque AN - OPUS4-607 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Riedel, Jens A1 - Hoekstra, S. A1 - Jäger, W. A1 - Gilijamse, J.J. A1 - van de Meerakker, S.Y.T. A1 - Meijer, G. T1 - Accumulation of Stark-decelerated NH molecules in a magnetic trap N2 - Here we report on the accumulation of ground-state NH molecules in a static magnetic trap. A pulsed supersonic beam of NH (a1Δ) radicals is produced and brought to a near standstill at the center of a quadrupole magnetic trap using a Stark decelerator. There, optical pumping of the metastable NH radicals to the X3Σ- ground state is performed by driving the spin-forbidden A3Π ← a1Δ transition, followed by spontaneous A → X emission. The resulting population in the various rotational levels of the ground state is monitored via laser induced fluorescence detection. A substantial fraction of the groundstate NH molecules stays confined in the several milliKelvin deep magnetic trap. The loading scheme allows one to increase the phase-space density of trapped molecules by accumulating packets from consecutive deceleration cycles in the trap. In the present experiment, accumulation of six packets is demonstrated to result in an overall increase of only slightly over a factor of two, limited by the trap-loss and reloading rates. KW - Cold matter KW - Stark deceleration KW - Trapping of polar molecules KW - NH KW - High resolution spectroscopy KW - Fluorescence KW - Radical PY - 2011 DO - https://doi.org/10.1140/epjd/e2011-20082-7 SN - 1434-6060 VL - 65 IS - 1-2 SP - 161 EP - 166 PB - Springer CY - Berlin AN - OPUS4-25050 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Kromm, Arne A1 - Kannengießer, Thomas A1 - Gibmeier, J. A1 - Genzel, C. A1 - Mee, V. van der T1 - Determination of Residual Stresses in Low Transformation Temperature (LTT-) Weld Metals using X-ray and High Energy Synchrotron Radiation KW - Filler material KW - Low transformation temperature KW - Synchrotron radiation KW - Phase specific residual stresses KW - Energy dispersive diffraction PY - 2007 IS - II-1658r1-07 SP - 1 EP - 17 PB - International Institute of Welding CY - Paris AN - OPUS4-15716 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kromm, Arne A1 - Kannengießer, Thomas A1 - Gibmeier, J. A1 - Genzel, C. A1 - Van der Mee, V. T1 - Determination of residual stresses in low transformation temperature (LTT -) welds metals using X-rayand high energy synchrotron radiation N2 - Crack and fatigue resistance are relevant evaluation criteria for welded joints and are decreased by tensile residual stresses resulting from the welding and cooling process, while compressive residual stresses can have a positive influence on the characteristics mentioned. In order to generate compressive residual stresses, a set of post weld treatment procedures is available, like shot peening, hammering, etc. These procedures have the disadvantage that they are time and cost extensive and have to be applied after welding. As another point, such technologies can only produce compressive stresses at the top surface, i.e. can only contribute to the reduction of the risk of cracks initiated at the surface, like fatigue cracks. A chance to generate compressive stresses over the complete weld joint during the welding procedure is offered by the so-called Low Transformation Temperature (LTT -) filler wires. Compared to conventional wires, these materials show lower phase transformation temperatures, which can work against coolingrelated tensile stresses, resulting from respective shrinkage restraint. In consequence, distinct compressive residual stresses can be observed within the weld and adjacent areas. The strength of these fillers makes them potentially applicable to high-strength steel welding. Welds produced with different LTT – filler wires have shown different levels and distributions of the resulting residual stresses depending on the specific transformation temperature. The transformation temperatures are determined by temperature measurement. Classical X-ray diffraction as well as diffraction methods using high energy synchrotron radiation have been used for residual stress analysis. By means of high energy synchrotron diffraction in reflection mode residual stress depth gradients can be determined nondestructively. The phase selective nature of the diffraction measurements enables the simultaneous determination of the phase specific residual stresses of all contributing crystalline phases within one experiment. The application of white beam diffraction implies recording of a multitude of diffraction lines within the energy range of the provided energy spectrum of the white beam. By this means phase specific residual stress depth distributions up to distances of 150 ìm below the surface can be analysed for steel using the energy dispersive set-up of the HMI-beamline EDDI at the Bessy site, Berlin, providing an energy range between 20-150 keV. As a side effect quantitative phase analysis can be carried out using white energy dispersive diffraction e.g. the determination of the content of retained austenite in the weld. KW - Filler materials KW - Low temperature KW - Reference lists KW - Residual stresses KW - Temperature KW - Transformation KW - Synchrotron radiation KW - Phase specific residual stresses KW - Energy dispersive diffraction PY - 2009 SN - 0043-2288 SN - 1878-6669 VL - 53 IS - 1/2 SP - 3 EP - 16 PB - Springer CY - Oxford AN - OPUS4-19214 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jablonka, Kevin Maik A1 - Ai, Qianxiang A1 - Al-Feghali, Alexander A1 - Badhwar, Shruti A1 - Bocarsly, Joshua D. A1 - Bran, Andres M. A1 - Bringuier, Stefan A1 - Brinson, L. Catherine A1 - Choudhary, Kamal A1 - Circi, Defne A1 - Cox, Sam A1 - de Jong, Wibe A. A1 - Evans, Matthew L. A1 - Gastellu, Nicolas A1 - Genzling, Jerome A1 - Gil, María Victoria A1 - Gupta, Ankur K. A1 - Hong, Zhi A1 - Imran, Alishba A1 - Kruschwitz, Sabine A1 - Labarre, Anne A1 - Lála, Jakub A1 - Liu, Tao A1 - Ma, Steven A1 - Majumdar, Sauradeep A1 - Merz, Garrett W. A1 - Moitessier, Nicolas A1 - Moubarak, Elias A1 - Mouriño, Beatriz A1 - Pelkie, Brenden A1 - Pieler, Michael A1 - Ramos, Mayk Caldas A1 - Ranković, Bojana A1 - Rodriques, Samuel G. A1 - Sanders, Jacob N. A1 - Schwaller, Philippe A1 - Schwarting, Marcus A1 - Shi, Jiale A1 - Smit, Berend A1 - Smith, Ben E. A1 - Van Herck, Joren A1 - Völker, Christoph A1 - Ward, Logan A1 - Warren, Sean A1 - Weiser, Benjamin A1 - Zhang, Sylvester A1 - Zhang, Xiaoqi A1 - Zia, Ghezal Ahmad A1 - Scourtas, Aristana A1 - Schmidt, K. J. A1 - Foster, Ian A1 - White, Andrew D. A1 - Blaiszik, Ben T1 - 14 examples of how LLMs can transform materials science and chemistry: a reflection on a large language model hackathon N2 - Large-language models (LLMs) such as GPT-4 caught the interest of many scientists. Recent studies suggested that these models could be useful in chemistry and materials science. To explore these possibilities, we organized a hackathon. This article chronicles the projects built as part of this hackathon. Participants employed LLMs for various applications, including predicting properties of molecules and materials, designing novel interfaces for tools, extracting knowledge from unstructured data, and developing new educational applications. The diverse topics and the fact that working prototypes could be generated in less than two days highlight that LLMs will profoundly impact the future of our fields. The rich collection of ideas and projects also indicates that the applications of LLMs are not limited to materials science and chemistry but offer potential benefits to a wide range of scientific disciplines. KW - Large Language model KW - Hackathon KW - Concrete KW - Prediction KW - Inverse Design KW - Orchestration PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-589961 DO - https://doi.org/10.1039/d3dd00113j VL - 2 IS - 5 SP - 1233 EP - 1250 PB - Royal Society of Chemistry (RSC) AN - OPUS4-58996 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Stephan, Ina A1 - Kutnik, M. A1 - Conti, E. A1 - Klamer, M. A1 - Nunes, L. A1 - van Acker, J. A1 - Plarre, Rüdiger T1 - Guidance on the European Biocidal Products Regulation concerning Efficacy of Wood Preservatives N2 - In Europe wood preservatives belong to Product Type 8 (PT8) of the Biocidal Products Regulation (BPR, EU n. 528/2012), which regulates the authorisation of biocidal active substances and products in the European market. The applicant, who aims to obtain authorization to place a product onto the European market, needs to submit data to substantiate the label claims for the intended uses. Label claims are a central issue in the assessment of efficacy. The aim of this paper is to raise awareness of the recently issued “Guidance on the Biocidal Products Regulation” concerning the evaluation of efficacy of wood preservatives. This guidance document is addressed to the applicants as well as to the competent authorities of the member states of Europe in charge of assessing efficacy data, and has been in the public domain, in its latest version, since February 2017. The CEN/Technical Committee 38 “Durability of wood and wood based products” / WG 22 "Performance, assessment and specification” decided to bring the Guidance to a wider audience with the aim of disseminating the information and to trigger discussion among the experts of IRGWP. An excerpt of the Guidance that is relevant to wood preservative products is presented in an Annex to this paper. Keywords: Biocidal Products Regulation, BPR, authorisation, Guidance, PT8, curative wood preservatives, preventive wood preservatives. T2 - IRG48 Scientific Conference on Wood Protection CY - Universität Ghent, Belgium DA - 04.06. 2017 KW - Preventive wood preservatives KW - Biocidal Products Regulation KW - BPR KW - Authorisation KW - Guidance KW - PT8 KW - Curative wood preservatives PY - 2017 SN - 2000-8953 SP - IRG/WP 17-20627-1 EP - 17 AN - OPUS4-40576 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stawski, Tomasz A1 - Besselink, R. A1 - Chatzipanagis, K. A1 - Hövelmann, J. A1 - Benning, L. G. A1 - Van Driessche, E. S. T1 - Nucleation Pathway of Calcium Sulfate Hemihydrate (Bassanite) from Solution: Implications for Calcium Sulfates on Mars N2 - CaSO4 minerals (i.e., gypsum, anhydrite, and bassanite) are widespread in natural and industrial environments. During the last several years, a number of studies have revealed that nucleation in the CaSO4–H2O system is nonclassical, where the formation of crystalline phases involves several steps. Based on these recent insights, we have formulated a tentative general model for calcium sulfate precipitation from solution. This model involves primary species that are formed through the assembly of multiple Ca2+ and SO42– ions into nanoclusters. These nanoclusters assemble into poorly ordered (i.e., amorphous) hydrated aggregates, which in turn undergo ordering into coherent crystalline units. The thermodynamic (meta)stability of any of the three CaSO4 phases is regulated by temperature, pressure, and ionic strength, with gypsum being the stable form at low temperatures and low-to-medium ionic strengths and anhydrite being the stable phase at high temperatures and at lower temperature for high salinities. Bassanite is metastable across the entire phase diagram but readily forms as the primary phase at high ionic strengths across a wide range of temperatures and can persist up to several months. Although the physicochemical conditions leading to bassanite formation in aqueous systems are relatively well established, nanoscale insights into the nucleation mechanisms and pathways are still lacking. To fill this gap and to further improve our general model for calcium sulfate precipitation, we conducted in situ scattering measurements at small-angle X-ray scattering and wide-angle X-ray scattering and complemented these with in situ Raman spectroscopic characterization. Based on these experiments, we show that the process of formation of bassanite from aqueous solutions is very similar to the formation of gypsum: it involves the aggregation of small primary species into larger disordered aggregates, only from which the crystalline phase develops. These data thus confirm our general model of CaSO4 nucleation and provide clues to explain the abundant occurrence of bassanite on the surface of Mars (and not on the surface of Earth). KW - Gypsum' SAXS KW - Calcium sulfate KW - Bassanite KW - Nucleation PY - 2020 DO - https://doi.org/10.1021/acs.jpcc.0c01041 VL - 124 IS - 15 SP - 8411 EP - 8422 PB - American Chemical Society AN - OPUS4-50849 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Brieger, C. A1 - Melke, J. A1 - van der Bosch, N. A1 - Reinholz, Uwe A1 - Riesemeier, Heinrich A1 - de Oliveira Guilherme Buzanich, Ana A1 - Krishna Kayarkatte, M. A1 - Schoeckel, A. A1 - Roth, C. T1 - A combined in-situ XAS-DRIFTS study unraveling adsorbate induced changes on the Pt nanoparticle structure N2 - The adsorption behavior of Platinum nanoparticles was studied for the as-received catalyst (under inert gas), under hydrogen and CO atmosphere using our newly designed in-situ cell. X-ray Absorption Spectroscopy (XAS) and Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) experiments were performed simultaneously with high data quality. Structural information and the type of adsorbate could be revealed via Extended X-ray Absorption Fine Structure (EXAFS) analysis, Dl X-ray Absorption Near Edge Structure analysis (Dl XANES) and in-situ DRIFTS. The as-received catalyst showed sub-surface oxygen and O(n-fold). Under CO atmosphere only CO(atop) was found. Reversible adsorbate induced changes of the Pt nanoparticle structure were derived from changes in the PtAPt coordination number and the corresponding bond distance. Under reducing conditions (H2, CO) a significant increase in both values occurred. Temperature dependent desorption of CO revealed a gradual shift from PtACO to PtAO. Reoxidation was clearly assigned to strong metal support interaction from the SiO2 support. KW - X-ray absorption spectroscopy KW - DRIFTS KW - XANES KW - CO adsorption KW - Platinum KW - Strong metal support interaction KW - Silica support KW - Adsorbates KW - Infrared spectroscopy PY - 2016 DO - https://doi.org/10.1016/j.jcat.2016.03.034 IS - 339 SP - 57 EP - 67 PB - Elsevier Inc. CY - Philadelphia, Pennsylvania, USA AN - OPUS4-35815 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hobohm, J. A1 - Kuchta, K. A1 - Krüger, Oliver A1 - van Wasen, Sebastian A1 - Adam, Christian T1 - Optimized elemental analysis of fluorescence lamp shredder waste N2 - Fluorescence lamps contain considerable amounts of rare earth elements (REE). Several recycling procedures for REE recovery from spent lamps have been established. However, despite their economic importance, the respective recycling is scarce so far, with an REE recovery rate of less than 1%. A reliable analysis of REE and other relevant metals like Yttrium is crucial for a thorough and complete recovery process. This applies both to the solid matter and aqueous phase, since most of the recycling processes include wet-chemical steps. We tested seven different reagent mixtures for microwave-assisted digestion of fluorescent lamp shredder, including hydrofluoric acid, perchloric acid, and hydrogen peroxide. We determined the concentrations of 25 of the most relevant rare earth and other trace elements (Al, P, Ti, V, Cr, Fe, Ni, Cu, Ga, Ge, As, Y, Ag, Cd, Sn, Sb, La, Ce, Eu, Gd, Tb, W, Au, Hg, and Pb) in the respective dilutions. Two independent digestions, one a mixture of perchlorid/nitric/hydrofluoric acid and the other aqua regia, showed the highest concentrations of 23 of these elements, excluding only Sn and Tb. The REE concentrations in the tested lamp shredder sample (stated in g/kg) were 10.2 (Y), 12.1 (La), 7.77 (Ce), 6.91 (Eu), 1.90 (Gd), and 4.11 (Tb). KW - Yttrium KW - Rare earth elements KW - Elemental analysis KW - Microwave-assisted digestion PY - 2016 DO - https://doi.org/10.1016/j.talanta.2015.09.068 SN - 0039-9140 VL - 147 SP - 615 EP - 620 PB - Elsevier CY - Amsterdam AN - OPUS4-34992 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Genga, R. M. A1 - Cornish, L. A. A1 - Woydt, Mathias A1 - van Vuuren, J. A1 - Polese, C. T1 - NbC: A machining alternative for dry and MQL face-milling of grey cast rion (GCI) N2 - NbC was studied as the major carbide phase with Ni and Co binders, produced by both spark plasma sintering (SPS) and liquid phase sintering (LPS), and tested as cutting inserts during dry and MQL (Minimum quantity lubrication) face-milling of grey cast iron (GCI) (BS 1452, Grade 17). T2 - World PM2016 CY - Hamburg, Germany DA - 09.10.2016 KW - Niobium carbide KW - NbC KW - Machining KW - Spark plasma sintering (SPS) KW - Liquid phase sintering (LPS) PY - 2016 SN - ISBN 978-1-899072-47-7 SP - 1 EP - 6 AN - OPUS4-37889 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schmidt, Martin A1 - Wu, D. A1 - Norman, F. A1 - Vanierschot, M. A1 - Verplaetsen, F. A1 - Berghmans, J. A1 - van den Bulck, E. T1 - Numerical investigation on the self-ignition behaviour of coal dust accumulations: The roles of oxygen, diluent gas and dust volume N2 - Self-ignition of coal dust deposits poses a higher risk of fires in oxygen-enriched oxy-fuel combustion systems. In this work, we develop a numerical method, using the commercial software COMSOL Multiphysics, to investigate self-ignition behaviour of coal dust accumulations with a main emphasis on the roles of oxygen, diluent gas and dust volume. A one-step 2nd-order reaction kinetic model considering both coal density and oxygen density is used to estimate reaction rate using the kinetic parameters from previously conducted hot-oven tests. This model is validated to predict the transient temperature and concentration profiles of South African coal dusts until ignition. The computed self-ignition temperatures of dust volumes show a good agreement with experimental results. In addition, it is found that the inhibiting effect of carbon dioxide is comparatively small and oxygen consumption increases dramatically after ignition. Parameter analysis shows that the heating value and kinetic parameters have a comparatively pronounced effect on self-ignition temperature. The model provides a satisfactory explanation for the dependence of self-ignition behaviour on gas atmospheres, thus helping to further understand the fire risk of self-ignition in oxy-fuel combustion systems. KW - Ignition temperature KW - Oxy-fuel combustion KW - Fire safety KW - Self-ignition KW - Numerical simulation PY - 2017 DO - https://doi.org/10.1016/j.fuel.2016.10.063 SN - 0016-2361 SP - 500 EP - 510 AN - OPUS4-37885 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Genga, R. A1 - Cornish, L. A1 - Woydt, Mathias A1 - van Vuuren, A. J. A1 - Polese, C. T1 - Face-milling of grey cast iron (BS 1452) using WC-based and NbC-based cutting tools N2 - NbC was studied as the major carbide phase with Ni and Co binders, produced by both spark plasma sintering (SPS) and liquid phase sintering (LPS), and tested as cutting inserts during dry and MQL (Minimum quantity lubrication) face-milling of gey cast iron (GCI) (BS 1452, Grade 17). T2 - 10th Tool Conference 2016 - TOOL 2016 CY - Bratislava, Slovakia DA - 04.10.2016 KW - NbC KW - Spark plasma sintering KW - Ni KW - Mechanical properties KW - Flank wear KW - Chemical stability PY - 2016 SN - ISBN 978-3-200-04786-0 SP - 336 EP - 342 AN - OPUS4-37869 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Adam, Christian A1 - Hobohm, J. A1 - Kuchta, K. A1 - van Wasen, Sebastian A1 - Krüger, Oliver T1 - Recovery of rare earth elements - optimized elemental analysis of fluorescent lamp shredder waste N2 - Rare earth elements (REE) are a crucial component of fluorescence lamps. Several procedures have been developed to recovery these technological important elements. Nevertheless, actual REE recycling from fluorescence lamps is scarce so far (recovery rate of less than 1 %), with current recycling approaches concentrating on glass recovery. Since most recycling processes include several, also wet-chemical steps, a complete knowledge of the actual elemental composition of the respective mass flows is necessary for an efficient REE recovery. We tested seven different reagent mixtures for microwave-assisted digestion of fluorescent lamp shredder, including HF, HClO4, and H2O2. We determined the concentrations of 25 of the most relevant rare earth and other trace elements in the respective dilutions. Two independent digestions, one a mixture of perchlorid/nitric/hydrofluoric acid and the other aqua regia, showed the highest concentrations of 23 of these elements, excluding only Sn and Tb. The REE concentrations in the tested lamp shredder sample (stated in g/kg) were 10.2 (Y), 12.1 (La), 7.77 (Ce), 6.91 (Eu), 1.90 (Gd), and 4.11 (Tb). T2 - 5th International conference industrial and hazardous waste management - Crete 2016 CY - Chania, Crete, Greece DA - 27.09.2016 KW - Rare earth elements KW - Critical raw materials KW - Resource recovery KW - WEEE PY - 2016 SN - 978-960-8475-20-5 SN - 2241-3138 SP - 1 EP - 4 AN - OPUS4-37761 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Brieger, C. A1 - Melke, J. A1 - van der Bosch, N. A1 - Reinholz, Uwe A1 - Riesemeier, Heinrich A1 - de Oliveira Guilherme Buzanich, Ana A1 - Krishna Kayarkatte, M. A1 - Derr, I. A1 - Schökel, A. A1 - Roth, C. ED - de Oliveira Guilherme Buzanich, Ana T1 - A combined in-situ XAS–DRIFTS study unraveling adsorbate induced changes on Pt nanoparticle structure N2 - The adsorption behavior of Platinum nanoparticles was studied for the as-received catalyst (under inert gas), under hydrogen and CO atmosphere using our newly designed in-situ cell. X-ray Absorption Spectroscopy (XAS) and Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) experiments were performed simultaneously with high data quality. Structural information and the type of adsorbate could be revealed via Extended X-ray Absorption Fine Structure (EXAFS) analysis, Δμ X-ray Absorption Near Edge Structure analysis (Δμ XANES) and in-situ DRIFTS. The as-received catalyst showed sub-surface oxygen and O(n-fold). Under CO atmosphere only CO(atop) was found. Reversible adsorbate induced changes of the Pt nanoparticle structure were derived from changes in the Pt-Pt coordination number and the corresponding bond distance. Under reducing conditions (H2, CO) a significant increase in both values occurred. Temperature dependent desorption of CO revealed a gradual shift from Pt-CO to Pt-O. Reoxidation was clearly assigned to strong metal support interaction from the SiO2 support. KW - X-ray absorption spectroscopy KW - DRIFTS KW - XANES KW - CO adsoprtion KW - Platinum KW - String metal support interaction KW - Silica support KW - Adsorbates KW - Infrared spectroscopy PY - 2016 DO - https://doi.org/10.1016/j.jcat.2016.03.034 SN - 0021-9517 VL - 339 SP - 57 EP - 67 PB - Elsevier AN - OPUS4-38367 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Severin, M. A1 - Breuer, J. A1 - Rex, M. A1 - Stemann, Jan A1 - Adam, Christian A1 - Van den Weghe, H. A1 - Kücke, M. T1 - Phosphate fertilizer value of heat treated sewage sludge ash N2 - This study focuses on the question whether heat treated sewage sludge ashes are more favourable as fertilizers than untreated sewage sludge ashes (USSA) and whether their fertilization effects are comparable with commercial triple superphosphate (TSP). In a pot experiment, maize was fertilized either with one of three heat treated and Na-, Ca- and Si-compounds amended sewage sludge ashes (two glown phosphates, steel mill slag + sewage sludge ash) or USSA or TSP as control. Fertilization with USSA did not increase the biomass yield and the P uptake of maize in comparison to the P0 treatment (7.25 resp. 8.35 g dry matter/pot). Fertilization with heat treated sewage sludge ashes and TSP resulted in significantly higher yields and plant P uptakes which are on average eight times higher than treatment with USSA and P0 control. Biomass yields and P uptake of maize after fertilization with heat treated sewage sludge ashes are not significantly different from those after TSP fertilization. The main P compound in USSA is Ca3(PO4)2. By heat treatment and amendment with different sodium, calcium, sulphur and silicon containing additives or steel mill converter slag, Ca3(PO4)2 is converted to Ca- and Na-silico-phosphates, which have a higher water solubility than Ca3(PO4)2. This increased solubility is responsible for the high plant availability of this phosphates. KW - P recycling KW - Sustainability KW - P solubility PY - 2014 UR - http://www.agriculturejournals.cz/publicFiles/138177.pdf SN - 1214-1178 SN - 1805-9368 VL - 60 IS - 12 SP - 555 EP - 561 PB - Inst. CY - Prague AN - OPUS4-32147 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gravenkamp, Hauke A1 - Birk, C. A1 - Van, J. T1 - Modeling ultrasonic waves in elastic waveguides of arbitrary cross-section embedded in infinite solid medium N2 - An approach is presented to model elastic waveguides of arbitrary cross-section coupled to infinite solid media. The formulation is based on the scaled boundary-finite element method. The surrounding medium is approximately accounted for by a dashpot boundary condition derived from the acoustic impedances of the infinite medium. It is discussed under which circumstances this approximation leads to sufficiently accurate results. Computational costs are very low, since the surrounding medium does not require discretization and the number of degrees of freedom on the cross-section is significantly reduced by utilizing higher-order spectral elements. KW - Guided waves KW - Scaled boundary finite element method KW - Leaky waves KW - Ultrasound PY - 2015 DO - https://doi.org/10.1016/j.compstruc.2014.11.007 SN - 0045-7949 SN - 0366-7138 VL - 149 SP - 61 EP - 71 PB - Pergamon Press CY - Oxford AN - OPUS4-32348 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Vanrostenberghe, S. A1 - Clarin, M. A1 - Shin, Y. A1 - Droesbeke, B. A1 - Van der Mee, V. A1 - Doré, M. A1 - Marquis, G. A1 - Parantainen, J. A1 - Kannengießer, Thomas A1 - Barsoum, Z. T1 - Improving the fatigue life of high strength steel welded structures by post weld treatments and specific filler materials (FATWELDHSS) N2 - The objective of the FATWELDHSS project was to study post-weld treatment techniques and their effect on the fatigue life of MAG welded attachments in High Strength Steel (HSS). Fatigue cracks in steel structures often occur at welded joints, where stress concentrations due to the joint geometry and tensile residual stresses are relatively high. Fatigue life improvement techniques, which rely on improving the stress field and/or the surface geometry around the welded joints, are generally known to be beneficial. Therefore, within the framework of this project, the following were examined: diode laser weld toe re-melting; High Frequency Mechanical Impact (HFMI) treatment; Low Transformation Temperature (LTT) filler wires Laser diode re-melting was used to improve the surface profile at the weld toe and thus reduce stress concentrations. HFMI treatment involving high frequency hammering of the weld toe is another technique that can produce a smooth weld toe profile but, more significantly, which also can introduce compressive residual stresses. Lastly, two new LTT filler wires were developed within the project as these can decrease or even remove tensile residual stresses resulting from weld zone shrinkage. An extensive fatigue testing programme was set up to establish the levels of improvement in the fatigue lives of the welded attachments achieved by application of the selected improvement techniques. Furthermore, two industrial demonstrators were selected that could show the project achievements in terms of facilitating the introduction of high strength steels by overcoming the limitations posed by the fatigue properties of the welded joints. In addition, modelling tools were developed to predict the residual stresses at the welded joint. Finally, practical guidelines were developed for enhancing the fatigue strength of HSS welded structures PY - 2015 SN - 978-92-79-44077-9 DO - https://doi.org/10.2777/705266 IS - EUR26929EN CY - Brüssel AN - OPUS4-35076 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Oliver A1 - Adam, Christian A1 - Hobohm, J. A1 - Basu, S. A1 - Kuchta, K. A1 - van Wasen, Sebastian T1 - Recycling oriented comparison of mercury distribution in new and spent fluorescent lamps and their potential risk N2 - This study compares the mercury distribution in the vapor phase, the phosphor powder and the glass matrix of new and spent fluorescent lamps. The spent fluorescent lamps were obtained at the collection yards of a public waste management company in Hamburg, Germany. An innovative systematic sampling method is utilized to collect six spent and eight corresponding new, off-the-shelf fluorescent lamp samples. The efficiency of several acid digestion methods for the determination of the elemental composition was studied and elemental mass fractions of K, Na, Y, Ca, Ba, Eu, Al, Pb, Mg, Hg, and P were measured. The study also finds aqua regia to be the best reagent for acid digestion. However, no significant difference in mercury distribution was found in the different phases of the new and spent fluorescent lamps. KW - Mercury KW - Rare earth elements KW - Hg distribution KW - Fluorescence lamps PY - 2017 DO - https://doi.org/10.1016/j.chemosphere.2016.11.104 SN - 0045-6535 SN - 1879-1298 VL - 169 SP - 618 EP - 626 PB - Elsevier AN - OPUS4-38481 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nieuwenkamp, G. A1 - Wessel, R. M. A1 - van der Veen, A.M.H. A1 - Ziel, P. R. A1 - Han, Q. A1 - Tuma, Dirk A1 - Woo, J.-C. A1 - Fuko, J.T. A1 - Szilágyi, N. A1 - Büki, T. A1 - Konopelko, L. A1 - Kustikov, Y.A. A1 - Popova, T.A. A1 - Pankratov, V.V. A1 - Pir, M.N. A1 - Nazarov, E.V. A1 - Ehvalov, L.V. A1 - Timofeev, A.U. A1 - Kuzmina, T.A. A1 - Meshkov, A.V. A1 - Valková, M. A1 - Pätoprsty, V. A1 - Downey, M. A1 - Vargha, G. A1 - Brown, A. A1 - Milton, M. T1 - International comparison CCQM-K77: Refinery gas N2 - Refinery gas is a complex mixture of hydrocarbons and non-combustible gases (e.g., carbon monoxide, carbon dioxide, nitrogen, helium). It is obtained as part of the refining and conversion of crude oil. This key comparison aims to evaluate the measurement capabilities for these types of mixtures. The results of the key comparison indicate that the analysis of a refinery-type gas mixture is for some laboratories a challenge. Overall, four laboratories (VSL, NIM, NPL and VNIIM) have satisfactory results. The results of some participants highlight some non-trivial issues, such as appropriate separation between saturated and unsaturated hydrocarbons, and issues with the measurement of nitrogen, hydrogen and helium. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCQM, according to the provisions of the CIPM Mutual Recognition Arrangement (MRA). DatesIssue 1A (Technical Supplement 2012) KW - Ringversuch KW - Raffineriegas KW - Chromatographische Analyse PY - 2012 DO - https://doi.org/10.1088/0026-1394/49/1A/08003 SN - 0026-1394 SN - 1681-7575 VL - 49 IS - 08003 SP - 1 EP - 71 PB - Inst. of Physics Publ. CY - Bristol AN - OPUS4-25931 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Karafiludis, Stephanos A1 - Scoppola, E. A1 - Wolf, S.E. A1 - Kochovski, Z. A1 - Matzdorff, D. A1 - Van Driessche, A. E. S. A1 - Hövelmann, J. A1 - Emmerling, Franziska A1 - Stawski, Tomasz M. T1 - Evidence for liquid-liquid phase separation during the early stages of Mg-struvite formation N2 - The precipitation of struvite, a magnesium ammonium phosphate hexahydrate (MgNH₄PO₄ · 6H₂O) mineral, from wastewater is a promising method for recovering phosphorous. While this process is commonly used in engineered environments, our understanding of the underlying mechanisms responsible for the formation of struvite crystals remains limited. Specifically, indirect evidence suggests the involvement of an amorphous precursor and the occurrence of multi-step processes in struvite formation, which would indicate non-classical paths of nucleation and crystallization. In this study, we use synchrotron-based in situ x-ray scattering complemented by cryogenic transmission electron microscopy to obtain new insights from the earliest stages of struvite formation. The holistic scattering data captured the structure of an entire assembly in a time-resolved manner. The structural features comprise the aqueous medium, the growing struvite crystals, and any potential heterogeneities or complex entities. By analysing the scattering data, we found that the onset of crystallization causes a perturbation in the structure of the surrounding aqueous medium. This perturbation is characterized by the occurrence and evolution of Ornstein-Zernike fluctuations on a scale of about 1 nm, suggesting a non-classical nature of the system. We interpret this phenomenon as a liquid-liquid phase separation, which gives rise to the formation of the amorphous precursor phase preceding actual crystal growth of struvite. Our microscopy results confirm that the formation of Mg-struvite includes a short-lived amorphous phase, lasting >10 s. KW - Physical and theoretical chemistry KW - Non-classical crystallization KW - Struvite KW - Liquid-liquid-phase-separation KW - Nucleation KW - Crystallization KW - In-situ scattering PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-584766 DO - https://doi.org/10.1063/5.0166278 SN - 1089-7690 VL - 159 IS - 13 SP - 1 EP - 12 PB - AIP Publishing CY - Woodbury, NY AN - OPUS4-58476 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -