TY - CONF A1 - Reinsch, Stefan A1 - Waurischk, Tina A1 - Müller, Ralf A1 - Arendt, F. A1 - Sierka, M. A1 - Diegeler, A. T1 - A new robot-assisted compositional screening method N2 - The system Na2O.B2O3-SiO2 (NBS) is the basis of many industrial glass applications and therefore one of the most studied systems at all. Glass formation is possible over a wide compositional range, but the system also contains ranges of pronounced phase separation and crystallization tendency. Despite its importance, experimental data are limited to few compositional areas. The general understanding and modelling of glass formation, phase separation, and crystallization in this system would therefore be easier if small step melt series could be studied. The efficient melting of such glass series is now possible with the new robotic glass melting system at the Federal Institute for Materials Research and Testing (BAM, Division Glasses). Using three exemplary joins within this NBS system, the small step changes of glass transition temperature (Tg), crystallization behavior as well as glass density (Roh) was studied. Additionally, experimental Tg and Roh data were compared with their modeled counterparts using SciGlass and a newly developed DFT model, respectively. T2 - Annual meeting of the French Union for Science and Glass Technology (USTV) and the 96th Annual Meeting of the German Society of Glass Technology - USTV-DGG joint meeting. CY - Orléans, France DA - 22.06.2023 KW - Robot-assisted galss melting KW - Sodiumborosilicate glasses KW - Density KW - Glass transformation temperature KW - Property simulation PY - 2023 AN - OPUS4-58724 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Böcker, Wolfgang D. G. A1 - Bücker, Michael A1 - Reinsch, Stefan A1 - Unger, Brita T1 - Abschlussbericht zum Vorhaben Verbundwerkstoff - Mineralisiertes Holz - FKZ: 033 9829 - Förderschwerpunkt "Integrierter Umweltschutz im Bereich der Holzwirtschaft" des Bundesministeriums für Bildung, Wissenschaft, Forschung und Technologie, BMBF - Projektlaufzeit: 1.10.2000-30.9.2003 KW - Mineralisiertes Holz KW - Sol-Gel KW - Holz KW - Vakuumtränkung KW - Holzschutz KW - Biozide PY - 2004 SP - 1 EP - 94 CY - Berlin AN - OPUS4-12055 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bücker, Michael A1 - Böcker, Wolfgang D. G. A1 - Reinsch, Stefan A1 - Unger, Brita T1 - Alternativer Holzschutz KW - Holzschutz KW - Kieselsol KW - Biozide KW - Sol-Gel-Prozess PY - 2004 SN - 1435-1854 IS - 11 SP - 77 EP - 80 PB - Verl. f. Fachpublizistik CY - Stuttgart AN - OPUS4-6333 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dreßler, Martin A1 - Nofz, Marianne A1 - Malz, Frank A1 - Pauli, Jutta A1 - Jäger, Christian A1 - Reinsch, Stefan A1 - Scholz, G. T1 - Aluminum speciation and thermal evolution of aluminas resulting from modified Yoldas sols N2 - Aluminas resulting from sols prepared via a modified Yoldas procedure were studied with differential thermal analysis (DTA), differential thermal gravimetrie (DTG), 27Al nuclear magnetic resonance (27Al MAS NMR) and X-ray diffraction (XRD) concerning their thermal properties, aluminum speciation and phase content. Hydrolysis of aluminum-sec-butoxide in aluminum nitrate solutions allowed to prepare stable sols with varying NO3-/Al molar ratios, solids contents and pH values. Resulting sols contained different aluminum species including also Al13 polycations. Sol preparation conditions also determined aluminum speciation in solid products obtained after thermal treatments of gels obtained from these sols. Al13 polycations and AlO5 species were found to play an important role for thermally induced transformation from amorphous products via eta-Al2O3 to alpha-Al2O3. Intermediately formed eta-Al2O3 promotes the phase transformation to alpha-Al2O3. KW - Alumina KW - Modified Yoldas sols KW - 27Al nuclear magnetic resonance KW - Differential thermal analysis KW - X-ray diffraction PY - 2007 U6 - https://doi.org/10.1016/j.jssc.2007.06.018 SN - 0022-4596 SN - 1095-726X VL - 180 IS - 9 SP - 2409 EP - 2419 PB - Elsevier CY - San Diego, Calif. AN - OPUS4-16189 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Scholz, Philipp A1 - Wachtendorf, Volker A1 - Elert, Anna Maria A1 - Falkenhagen, Jana A1 - Becker, Roland A1 - Hoffmann, Katrin A1 - Resch-Genger, Ute A1 - Tschiche, Harald A1 - Reinsch, Stefan A1 - Weidner, Steffen ED - Scholz, Philipp T1 - Analytical toolset to characterize polyurethanes after exposure to artificial weathering under systematically varied moisture conditions N2 - Polyether and -ester urethanes (PU) were exposed to artificial weathering at 40 °C and artificial UV radiation in a weathering chamber. In 3 parallel exposures, humidity was varied between dry, humid, and wet conditions. Material alteration was investigated by various analytical techniques like size exclusion chromatography (SEC), liquid chromatography-infrared spectroscopy (LC-FTIR), thermal-desorption gas chromatography-mass spectrometry (TD-GC-MS), fluorescence mapping and dynamic mechanical analysis (DMA). Our results show that depending on the weathering conditions, different degradation effects can be observed. By means of SEC an initial strong decrease of the molar masses and a broadening of the mass distributions was found. After a material dependent time span this was followed by a plateau where molar mass changes were less significant. A minor moisture-dependent degradation effect was only found for polyester PU. Fluorescence measurements on two materials revealed an increase in the luminescence intensity upon weathering process reaching a saturation level after about 500 h. The changes in the optical properties observed after different exposure conditions and times were very similar. The TD-GC-MS data showed the fate of the stabilizers and antioxidant in the course of weathering. LC-FTIR measurements revealed a change in peak intensities and the ratio of urethane and carbonyl bands. KW - Polyurethane KW - Artificial weathering KW - Moisture KW - Crosslinking KW - Degradation PY - 2019 UR - https://www.sciencedirect.com/science/article/pii/S0142941819303708 U6 - https://doi.org/10.1016/j.polymertesting.2019.105996 SN - 0142-9418 VL - 78 SP - 105996, 1 EP - 9 PB - Elsevier CY - Amsterdam AN - OPUS4-48625 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kiefer, P. A1 - Maiwald, M. A1 - Deubener, J. A1 - Balzer, R. A1 - Behrens, H. A1 - Waurischk, Tina A1 - Reinsch, Stefan A1 - Müller, Ralf T1 - Automated Analysis of Slow Crack Growth in Hydrous Soda-Lime Silicate Glasses N2 - To explore the impact of ambient and structural water on static fatigue, the initiation and growth of 3279 Vickers induced median radial cracks were automatically recorded and analyzed. We find that humidity is more efficient in initiating cracks and promoting their growth than water, which is dissolved in the glass structure. In particular for slow crack growth (< 3x10-6 m s-1), tests in dry nitrogen showed a considerable decrease in the crack growth exponent with increasing water content of the glasses. On the other hand, if tests were performed in humid air, the crack growth exponent was independent of the water content of the hydrous glasses, while stress intensity decreased slightly. These observations indicate that water promotes the processes at the crack-tip regardless of its origin. However, ambient water is more efficient. KW - Indentation fracture toughness KW - Slow crack growth KW - Automated analysis KW - Hydrous glass KW - Vickers indentation PY - 2020 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:b43-513085 VL - 7 SP - 268 AN - OPUS4-51308 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Reinsch, Stefan A1 - Schadrack, Reinhard A1 - Müller, Ralf A1 - Behrens, H. A1 - Deubener, J. T1 - Bestimmung der Glastransformationstemperatur wasserhaltiger Gläser T2 - 80. Glastechnische Tagung CY - Dresden, Deutschland DA - 2006-06-12 PY - 2006 SN - 3-921089-46-8 SP - 1(?) EP - 5(?) PB - Verl. d. Dt. Glastechn. Ges. CY - Offenbach AN - OPUS4-12552 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Dreßler, Martin A1 - Nofz, Marianne A1 - Pauli, Jutta A1 - Jäger, Christian A1 - Scholz, G. T1 - Beziehungen zwischen Zusammensetzung und thermischen Eigenschaften von Alumo-Xerogelen T2 - Jahrestagung der Gesellschaft für thermische Analyse (GEFTA) CY - Braunschweig, Germany DA - 2004-10-04 PY - 2004 AN - OPUS4-5620 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dreßler, Martin A1 - Reinsch, Stefan A1 - Schadrack, Reinhard A1 - Benemann, Sigrid T1 - Burnout behavior of ceramic coated open cell polyurethane (PU) sponges N2 - Open cell rigid foams made from polyurethane (PU) are frequently used in ceramic processing for preparation of porous ceramics by the so-called replica technique. This work presents data regarding the PU burnout, shrinkage characteristics as well as the morphology of the ceramic coated PU sponges during heating up. Shrinkage of the ceramic coated PU sponges closely follows the mass loss due to PU decomposition. Two temperatures (i) 267 °C and (ii) 380 °C were identified at which PU decomposition reaches local maxima. Shrinkage measurements on ceramic coated PU sponges reveal that both PU decomposition stages lead to similar extends of shrinkage in the ceramic coated PU sponge. Differential thermal analysis (DTA) showed that the two decomposition related temperatures (267 and 380 °C) differ concerning the energy release. While the low-temperature signal is endothermic, an exothermic signal was detected at 380 °C. The morphology of the ceramic coated PU sponges was investigated with scanning electron microscopy (SEM) which gave insight into the formation of hollow ceramic struts-a well known feature of ceramics being prepared by the replica technique. KW - Polyurethane (PU) KW - Porous ceramics KW - Mass spectrometry KW - Thermal analysis PY - 2009 U6 - https://doi.org/10.1016/j.jeurceramsoc.2009.07.025 SN - 0955-2219 SN - 1873-619X VL - 29 IS - 16 SP - 3333 EP - 3339 PB - Elsevier CY - Oxford AN - OPUS4-20092 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Al-Terkawi, Abdal-Azim A1 - Scholz, G. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Reinsch, Stefan A1 - Kemnitz, E. A1 - Emmerling, Franziska T1 - Ca- and Sr- tetrafluoroisophthalates: mechanochemical synthesis, characterization, and ab initio structure determination N2 - New fluorinated coordination polymers were prepared mechanochemically by milling the alkaline earth metal hydroxides MII(OH)2·xH2O (MII: Ca, Sr) with tetrafluoroisophthalic acid (H2mBDC-F4). The structures of [{Ca(mBDC-F4)(H2O)2}·H2O] and [{Sr(mBDC-F4)(H2O)2}·H2O] were determined based on ab initio calculations and their powder X-ray diffraction (PXRD) data. The compounds are isomorphous and crystallize in the orthorhombic space group P212121. The determined structures were validated by using extended X-ray absorption (EXAFS) data. The new materials were thoroughly characterized using elemental analysis, thermal analysis, magic angle spinning NMR, and attenuated total reflection-infrared spectroscopy. Further characterization methods such as BET, dynamic vapor sorption, and scanning electron microscopy imaging were also used. Our investigations indicate that mechanochemistry is an efficient method for preparing such materials. KW - Mechanochemistry KW - In situ KW - XRD KW - Coordination polymers PY - 2017 UR - http://pubs.rsc.org/-/content/articlehtml/2017/dt/c7dt00734e U6 - https://doi.org/10.1039/c7dt00734e VL - 46 IS - 18 SP - 6003 EP - 6012 AN - OPUS4-41516 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Unger, Brita A1 - Bücker, Michael A1 - Reinsch, Stefan A1 - Hübert, Thomas T1 - Chemical aspects of wood modification by sol-gel-derived silica N2 - It has been shown that tetraethoxysilane-derived precursors are suitable solutions for impregnating pine sapwood to improve its dimensional stability. Tailored sol–gel syntheses result in precursors with nano-scaled silica species which are able to penetrate into the cell walls of wood. The physical fixation of those species inside the cell walls was verified by ESEM/EDX investigations. There is evidence that the silica species are chemically bonded to wood components. Nonreacted alkoxy groups can exist in the wood composites after impregnation. The amount of these organic residues depends on the composition of the precursors, especially their condensation degree and reactivity. Treatments for finishing the composites after the impregnation step to get clean products and stable properties are discussed in this context. An explanation of the complex relationship between solids content in the impregnation solutions and percentage weight gain and bulking of the composites is given. It can be demonstrated that high WPG values (>20 %) are pre-conditions for an effective protection of the resulting composites but they only guarantee efficient improvements if connected with the incorporation of the inorganic component inside the cell walls. Therefore, the sol–gel syntheses have to be carried out in such a manner that very small (<2 nm) as well as reactive species are sufficiently available. This demands syntheses using sub-stoichiometric water contents (H2O/TEOS <4, better <2). KW - Silica-wood composites KW - Sol-gel derived precursors KW - Curing KW - Fixation of silica KW - Dimensional stability PY - 2013 U6 - https://doi.org/10.1007/s00226-012-0486-7 SN - 0043-7719 SN - 1432-5225 VL - 47 IS - 1 SP - 83 EP - 104 PB - Springer CY - Berlin AN - OPUS4-26258 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Waurischk, Tina A1 - Müller, Ralf A1 - Reinsch, Stefan A1 - Kiefer, P. A1 - Deubener, J. A1 - Balzer, R. A1 - Behrens, H. T1 - Crack Growth in Hydrous Soda-Lime Silicate Glass N2 - Stable crack growth was measured for nominal dry and water-bearing (6 wt%) soda-lime silicate glasses in double cantilever beam geometry and combined with DMA studies on the effects of dissolved water on internal friction and glass transition, respectively. In vacuum, a decreased slope of logarithmic crack growth velocity versus stress intensity factor is evident for the hydrous glass in line with an increase of b-relaxation intensity indicating more energy Dissipation during fracture. Further, inert crack growth in hydrous glass is found to be divided into sections of different slope, which indicates different water related crack propagation mechanism. In ambient air, a largely extended region II is observed for the hydrous glass, which indicates that crack growth is more sensitive to ambient water. KW - Internal friction KW - Soda-lime silicate glass KW - Water content KW - Stable crack growth KW - DCB geometry KW - Stress intensity factor PY - 2020 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:b43-506829 VL - 7 SP - Articel 66 AN - OPUS4-50682 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Reinsch, Stefan A1 - Nascimento, M.L.F. A1 - Müller, Ralf A1 - Zanotto, E. D. T1 - Crystal growth kinetics in cordierite and diopside glasses in wide temperature ranges N2 - We measured and collected literature data for the crystal growth rate, u(T), of µ-cordierite (2MgO · 2Al2O3 · 5SiO2) and diopside (CaO · MgO · 2SiO2) in their isochemical glass forming melts. The data cover exceptionally wide temperature ranges, i.e. 800–1350 °C for cordierite and 750–1378 °C for diopside. The maximum of u(T) occurs at about 1250 °C for both systems. A smooth shoulder is observed around 970 °C for µ-cordierite. Based on measured and collected viscosity data, we fitted u(T) using standard crystal growth models. For diopside, the experimental u(T) fits well to the 2D surface nucleation model and also to the screw dislocation growth mechanism. However, the screw dislocation model yields parameters of more significant physical meaning. For cordierite, these two models also describe the experimental growth rates. However, the best fittings of u(T) including the observed shoulder, were attained for a combined mechanism, assuming that the melt/crystal interface growing from screw dislocations is additionally roughened by superimposed 2D surface nucleation at large undercoolings, starting at a temperature around the shoulder. The good fittings indicate that viscosity can be used to assess the transport mechanism that determines crystal growth in these two systems, from the melting point Tm down to about Tg, with no sign of a breakdown of the Stokes–Einstein/Eyring equation. KW - Crystal growth KW - Oxide glasses KW - Silicates KW - Kristallwachstumsgeschwindigkeit KW - Kinetik KW - Silikatgläser PY - 2008 U6 - https://doi.org/10.1016/j.jnoncrysol.2008.09.007 SN - 0022-3093 VL - 354 IS - 52-54 SP - 5386 EP - 5394 PB - North-Holland Publ. Co. CY - Amsterdam AN - OPUS4-18383 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Nascimento, M.L.F. A1 - Zanotto, E. D. T1 - Crystal Growth Mechanism in Cordierite and Diopside Glasses in Wide Temperature Ranges T2 - XX. International Congress on Glass CY - Kyoto, Japan DA - 2004-09-26 KW - Cordierite KW - Diopside KW - Glass KW - Crystal growth PY - 2004 SP - 6 pages PB - Ceramic Society of Japan CY - Tokio AN - OPUS4-4389 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Nascimento, M.L.F. A1 - Zanotto, E. D. T1 - Crystal Growth Mechanism in Cordierite and Diopside Glasses in wide Temperature Ranges T2 - XX. International Congress on Glass CY - Kyoto, Japan DA - 2004-09-26 PY - 2004 AN - OPUS4-5622 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nagamine, K. A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Honma, T. A1 - Komatsu, T. T1 - Crystallization behavior of lithium iron phosphate glass powders in different atmospheres N2 - Crystallization behavior in different atmospheres (air, Ar, and 7% H2/Ar) of lithium iron phosphate glass (33Li2O–33Fe2O3–1Nb2O5–33P2O5 (LFNP)) powders with different sizes of 2–1000 µm was examined. The crystallization peak temperature (Tp) in Ar and 7% H2/Ar decreased with decreasing the particle size of glass powders, but the value of Tp in air was independent of particle size. The crystallized glass obtained by heating to Tp showed the formation of the α-Li3Fe2(PO4)3 and LiFePO4 crystalline phases. Fe2O3 crystals were formed only in the inside of crystallized glass plates in the heating in air. The crystallization of LiFePO4 was largely enhanced in the particle size of <2 µm during the heating in Ar and 7% H2/Ar atmospheres. The main crystallization mechanism in LFNP glass was found to be surface crystallization. Significant shrinkages were observed for glass compacts (pellets) in the heating in 7% H2/Ar. These results suggest that controlling particle sizes and atmospheres enables the design the morphology of LiFePO4 crystals in LFNP glass. KW - DTA KW - Kristallisation KW - Phasenentwicklung KW - Unterschiedliche Atmosphären KW - Lithiumionen-Batterie PY - 2011 U6 - https://doi.org/10.1111/j.1551-2916.2011.04579.x SN - 0002-7820 SN - 1551-2916 VL - 94 IS - 9 SP - 2890 EP - 2895 PB - Blackwell Publishing CY - Malden AN - OPUS4-24914 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Rosemann, Maik A1 - Müller, Ralf A1 - Deubener, J. T1 - Crystallization of glass matrix composites for LTCC T2 - TC7-Meeting im Rahmen der Crystallization 2009, 9th Intern. Symp. on Crystallization in Glasses and Liquids CY - Curitiba, Brazil DA - 2009-09-10 PY - 2009 AN - OPUS4-20211 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Waurischk, Tina A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Chen, Y.-F. A1 - Contreras Jaimes, A. T1 - Datengetriebener Workflow für die beschleunigte Entwicklung von Glas (GlasDigital) N2 - Das Projekt GlasDigital wurde im allgemeinen vorgestellt, sowie die einzelnen Zwischenstände der verschiedenen Arbeitspakete aller Projektpartner präsentiert. Die allgemeine Porjektvorstellung ist auf deutsch. Die Zwischenstände der Arbeitsinhalte sind auf englisch. T2 - PMD Vollversammlung CY - Berlin, Germany DA - 03.11.2022 KW - Oxidglas KW - Robotische Glasschmelzanlage KW - ML KW - Ontologie KW - Digitaler Zwilling KW - Bildanalyse PY - 2022 AN - OPUS4-56491 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kiefer, P. A1 - Balzer, R. A1 - Deubener, J. A1 - Behrens, H. A1 - Waurischk, Tina A1 - Reinsch, Stefan A1 - Müller, Ralf T1 - Density, elastic constants and indentation hardness of hydrous soda-lime silica glasses N2 - The effect of structural water on density, elastic constants and microhardness of water-bearing soda-lime-silica glasses of up to 21.5 mol% total water is studied. It is found that the Poisson ratio and the water content are positively correlated, while density and the elastic moduli decrease with increasing water content. Vickers hardness decreases by approximately 27% from the dry to the most hydrous glass. For water fractions <3 mol%, the dependencies are non-linear reflecting the non-linear change in the concentrations of OH and H2O molecules dissolved, whereas for water fractions >3 mol% linear dependencies are found. To distinguish the effect of structural water and environmental water, indentations were performed in toluene, nitrogen gas and air. Timedependent softening was evident for testing dry glasses in humid atmospheres as well as for tests of hydrous glasses in dry atmospheres. This indicates that the response times of dissolved water species are effectively equal in both scenarios. KW - Elastic constants KW - Soda-lime-silica KW - Glass KW - Water content KW - Microhardness PY - 2019 U6 - https://doi.org/10.1016/j.jnoncrysol.2019.119480 SN - 0022-3093 SN - 1873-4812 VL - 521 SP - 119480 PB - Elsevier B.V. AN - OPUS4-48758 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Böcker, Wolfgang D. G. A1 - Bücker, Michael A1 - Seeger, Stefan A1 - Unger, Brita ED - Specht, K. T1 - Development of wood-inorganic composites with enhanced properties and environmental stability T2 - 4th International Wood and Natural Fibre Composites Symposium CY - Kassel, Germany DA - 2002-04-10 PY - 2002 VL - 4 SP - 50-1-50-6 CY - Kassel AN - OPUS4-1365 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Böcker, Wolfgang D. G. A1 - Bücker, Michael A1 - Seeger, Stefan A1 - Unger, Brita T1 - Development of wood-inorganic composites with enhanced properties and environmental stability T2 - 4th International Wood and Natural Fibre Composites Symposium CY - Kassel, Germany DA - 2002-04-10 PY - 2002 AN - OPUS4-12336 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dreßler, Martin A1 - Nofz, Marianne A1 - Klobes, Peter A1 - Dörfel, Ilona A1 - Reinsch, Stefan T1 - Differences between films and monoliths of sol-gel derived aluminas N2 - This work compares thin layers (films) and monoliths prepared from alumina sols with respect to their microstructure, thermal evolution, porosity and specific surface area. After heat treatment at similar temperatures, films and monoliths showed the same qualitative changes in porosity and specific surface area. However, some marked quantitative differences were detected. Film fragments had a lower open porosity, a lower specific surface area and a narrower pore size distribution. Furthermore, the thermal evolution showed a markedly different burnout of organic components between films and monoliths. The observed differences between films and monolith can be explained by the ageing history of the sols during sample preparation. KW - Sol-gel processing KW - Alumina KW - Phase transitions KW - Porosity PY - 2010 U6 - https://doi.org/10.1016/j.tsf.2010.07.057 SN - 0040-6090 VL - 519 IS - 1 SP - 42 EP - 51 PB - Elsevier CY - Amsterdam AN - OPUS4-22606 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Deubener, J. T1 - Dissolution of alumina in glass matrix composites T2 - Crystallization 2009, 9th Intern. Symp. on Crystallization in Glasses and Liquids CY - Curitiba, Brazil DA - 2009-09-10 PY - 2009 AN - OPUS4-20209 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Meszaros, R. A1 - Rosemann, Maik A1 - Eberstein, M. A1 - Müller, Ralf A1 - Deubener, J. T1 - Dissolution of Alumina, Sintering and Crystallization in Glass Ceramic Composites for LTCC T2 - Intern. Con. on Glass ICG 2010 CY - Bahia, Brazil DA - 2010-09-20 PY - 2010 AN - OPUS4-22293 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Müller, Ralf A1 - Meszaros, Robert A1 - Peplinski, Burkhard A1 - Reinsch, Stefan A1 - Eberstein, Markus A1 - Schiller, Wolfgang Arno A1 - Deubener, J. T1 - Dissolution of alumina, sintering, and crystallization in glass ceramic composites for LTCC KW - LTCC KW - Sintering KW - Crystallization KW - Alumina dissolution KW - Rietveld analysis PY - 2009 U6 - https://doi.org/10.1111/j.1551-2916.2009.03089.x SN - 0002-7820 SN - 1551-2916 VL - 92 IS - 8 SP - 1703 EP - 1708 PB - Blackwell Publishing CY - Malden AN - OPUS4-20676 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Deubener, J. A1 - Behrens, H. T1 - DMTA study of hydrated soda-lime-silicate glasses T2 - Thermal Analysis and Calorimetry in Industry and Research - 40 Years of GEFTA CY - Berlin, Germany DA - 2014-09-16 PY - 2014 AN - OPUS4-32343 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Eberstein, Markus A1 - Thiel, A. A1 - Deubener, J. A1 - Schiller, Wolfgang Arno T1 - Effect of dispersed Al2O2-particles on sintering of glass matrix composites T2 - 10th International Conference and Exhibition of the European Ceramic Society CY - Berlin, Germany DA - 2007-06-17 PY - 2007 AN - OPUS4-15495 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Eberstein, Markus A1 - Deubener, J. A1 - Thiel, A. A1 - Schiller, Wolfgang Arno ED - J.G. Heinrich, ED - C.G. Aneziris, T1 - Effect of dispersed Al2O3 particles on sintering of glass matrix composites T2 - 10th International Conference of the European Ceramic Society CY - Berlin DA - 2007-06-17 KW - LTCC KW - Glass matrix composites KW - Inclusions KW - Sintering kinetics KW - Modelling PY - 2007 SN - 3-87264-022-4 SP - 290 EP - 295 PB - Göller CY - Baden-Baden AN - OPUS4-17445 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Müller, Ralf A1 - Eberstein, Markus A1 - Reinsch, Stefan A1 - Schiller, Wolfgang Arno A1 - Deubener, J. A1 - Thiel, A. T1 - Effect of rigid inclusions on sintering of low temperature co-fired ceramics KW - Sintering KW - Glass Matrix Composites KW - Rigid Inclusion KW - Effective Viscosity KW - Kinetic Modelling KW - LTCC PY - 2007 SN - 1753-3562 SN - 0017-1050 SN - 0031-9090 SN - 1750-6697 VL - 48 IS - 4 SP - 259 EP - 266 PB - Society of Glass Technology CY - Sheffield AN - OPUS4-16211 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Müller, Ralf A1 - Reinsch, Stefan A1 - Eberstein, Markus A1 - Deubener, J. A1 - Thiel, A. A1 - Schiller, Wolfgang Arno T1 - Effects of dispersed Al2O3 particles on sintering of LTCC N2 - The sintering of Low Temperature Co-fired Ceramics prepared from alumoborosilicate glass- and Al2O3 powders of similar small particle size was studied by dilatometry, heating microscopy, microstructure analysis, glass- and effective viscosity measurements. The steric effect of Al3O3 inclusions was studied using a gnon-reactiveh model composite. With increasing Al3O3 volume fraction (Φ ≤ 0.45), sintering decelerates and its final stage shifts to higher temperature. The attainable shrinkage is reduced as Al2O3 particle clusters bearing residual pores become more frequent. The kinetics of sintering could be described formally superposing the weighed contributions of differentially sized and randomly composed glass-crystal particle clusters and assuming a sintering rate controlled by the effective matrix viscosity, which increases with Φ and with progressive wetting of Al2O3 particles during densification. The "reactive" model composite shows significant dissolution of Al2O3 into the glass, which has two opposed effects on sintering: reducing Φ and increasing glass viscosity. For the present case (Φ = 0.25), the latter effect dominates and sintering is retarded by Al2O3 dissolution. Crystallization of wollastonite starts after full densification. Dissolution of Al2O3 was found to promote the subsequent growth of anorthite. KW - LTCC KW - Glass matrix composites KW - Al2O3-inclusions KW - Sintering kinetics PY - 2005 SN - 1022-6680 SN - 1662-8985 VL - 39-40 SP - 375 EP - 380 PB - Trans Tech Publ. CY - Zurich AN - OPUS4-18441 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Rothe, Stefan A1 - Erfurt, Darja A1 - Müller, Ralf T1 - Effects of milling on sinter-crystallization of alkaline earth silicate glass powders T2 - 23rd International Congress on Glass, ICG Prague 2013 CY - Prague, Czech Republic DA - 2013-07-01 PY - 2013 AN - OPUS4-28877 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Fest, Sarah Ute A1 - Müller, Ralf T1 - Effects of milling on sinter-crystallization of alkaline earth silicate glass powders T2 - 88. Glastechnische Tagung DGG - ACerS GOMD 2014 CY - Aachen, Germany DA - 2014-05-26 PY - 2014 AN - OPUS4-30811 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Eberstein, Markus A1 - Müller, Ralf A1 - Schiller, Wolfgang Arno A1 - Thiel, A. A1 - Deubener, J. T1 - Einflüsse mikrodisperser Al203-Einschlüsse auf die Sinterung von LTCC T2 - 82. Glastechn. Tagung CY - Hamelin, Germany DA - 2008-05-19 PY - 2008 AN - OPUS4-17648 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Bücker, Michael A1 - Böcker, Wolfgang D. G. A1 - Reinsch, Stefan A1 - Unger, Brita ED - Wielage, B. ED - Leonhardt, G. T1 - Entwicklung umweltverträglicher Holzverbundwerkstoffe mit verbesserter biologischer und Feuchtebeständigkeit T2 - Tagung "Verbundwerkstoffe und Werkstoffverbunde" CY - Chemnitz, Deutschland DA - 2001-09-05 PY - 2001 SN - 3-527-30319-7 SP - 463 EP - 467 PB - Wiley-VCH CY - Weinheim AN - OPUS4-1160 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Müller, Ralf A1 - Behrens, Harald A1 - Ageo-Blanco, Boris A1 - Reinsch, Stefan A1 - Wirth, Thomas T1 - Foaming Species and Trapping Mechanisms in Barium Silicate Glass Sealants N2 - Barium silicate glass powders 4 h milled in CO2 and Ar and sintered in air are studied with microscopy, total carbon analysis, differential thermal Analysis (DTA), vacuum hot extraction mass spectroscopy (VHE-MS), Fourier-transformed infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and time-of-flight secondary-ion mass spectrometry (TOF-SIMS). Intensive foaming of powder compacts is evident, and VHE studies prove that foaming is predominantly caused by carbonaceous species for both milling gases. DTA Shows that the decomposition of BaCO3 particles mix-milled with glass powders occurs at similar temperatures as foaming of compacts. However, no carbonate at the glass surface could be detected by FTIR spectroscopy, XPS, and TOF-SIMS after heating to the temperature of sintering. Instead, CO2 molecules unable to rotate identified by FTIR spectroscopy after milling, probably trapped by mechanical dissolution into the glass bulk. Such a mechanism or microencapsulation in cracks and particle aggregates can explain the contribution of Ar to foaming after intense milling in Ar atmosphere. The amount of CO2 molecules and Ar, however, cannot fully explain the extent of foaming. Carbonates mechanically dissolved beneath the surface or encapsulated in cracks and micropores of particle aggregates are therefore probably the major foaming source. KW - Milling KW - Foaming KW - Glass powder KW - Sintering PY - 2021 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:b43-531227 SN - 1438-1656 VL - 24 IS - 6 SP - 2100445-1 EP - 2100445-13 AN - OPUS4-53122 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Gaber, Martin A1 - Güther, Wolfgang A1 - Müller, Ralf A1 - Schiller, Wolfgang Arno T1 - Gassensorgeregelte Entbinderung keramischer Folien T2 - Symp. HLK 2009 CY - Aachen, Germany DA - 2009-03-23 PY - 2009 AN - OPUS4-18965 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan T1 - Glass N2 - Überblick über die Arbeitsschwerpunkte des Fachbereichs 5.6 Glas und die Vielfalt des Werkstoffs Glas. An Hand der Vakuumheißgasextraktion (VHE) werden einige Beispiele u.a. zur Bestimmung des Wassergehalts oder des Diffusionskoeffizienten von Wasserstoff in Gläsern gezeigt. Zum Schluss erfolgt ein Ausblick auf die im nächsten Jahr zur Verfügung stehende robotergestützte Glasscreening Anlage. N2 - Overview about the key activities of division 5.6 glass and the diversity of the material glass. For the vacuum hot extraction method (VHE-MS) some examples are presented e. g. for the measurement of water content or the determination of diffusion coefficient of hydrogen in glasses. Finally, an outlook is shown on the robot controlled glass screening device which will be available next year. T2 - BAM - IFW Workshop CY - Berlin, Germany DA - 25.11.2019 KW - Glass KW - Glass screening device KW - Vacuum hot extraction PY - 2019 AN - OPUS4-50452 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Deubener, J. A1 - Roessler, C. A1 - Bauer, Ute A1 - Behrens, H. T1 - Glass transition and viscosity of hydrous soda-lime-borate glasses N2 - Boron oxide glasses usually show low glass transition temperature Tg due to the three-fold oxygen coordination of boron. Adding of alkali and alkaline earth oxides to the glass composition will not decrease but increase Tg due to a change in boron coordination from trigonal to tetrahedral, known as the boron anomaly. Only for higher fractions of alkali oxides, non-bridging oxygens (NBO) are progressively formed in competition with tetrahedrally coordinated boron, which leads to a decrease in viscosity. ln contrast to this well-known behavior of alkali oxides (R2O), there is little known about adding H2O to borate glasses. The present work therefore aims in shedding light on the rheological properties of hydrous soda lime borate glasses with particular focus on the role of water. For doing so, we determined Tg as a function of Na2O and H2O content using differential thermal analysis (DTA) backed up by micropenetration viscosity measurements. Results show that water decreases Tg for all glasses and water concentrations under study (< 8 wt.% total water). Obviously, water mostly causes the formation of NBO having no significant influence on boron coordination as seen for alkaline. T2 - Crystallization 2015 CY - Shanghai, China DA - 07.04.2016 KW - Borate glasses KW - Thermal analyses KW - Viscosity KW - Water-bearing glasses PY - 2016 AN - OPUS4-38318 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Schadrack, Reinhard A1 - Müller, Ralf A1 - Behrens, H. A1 - Deubener, J. T1 - Glastransformationstemperatur wasserhaltiger Gläser T2 - 80. Glastechnische Tagung CY - Dresden, Germany DA - 2006-06-12 PY - 2006 AN - OPUS4-12485 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Reinsch, Stefan A1 - Müller, Ralf T1 - Herstellung von Gläsern mittlerer Wassergehalte T2 - 79. Glastechnische Tagung CY - Würzburg, Deutschland DA - 2005-05-23 KW - Glas KW - Wassergehalt PY - 2005 SN - 3-921089-43-3 SP - 4 Seiten PB - Deutsche Glastechnische Gesellschaft CY - Offenbach AN - OPUS4-7606 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Müller, Ralf T1 - Herstellung von Gläsern mittlerer Wassergehalte T2 - 79. Glastechnische Tagung CY - Würzburg, Germany DA - 2005-05-23 PY - 2005 AN - OPUS4-7805 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bücker, Michael A1 - Böcker, Wolfgang D. G. A1 - Reinsch, Stefan A1 - Unger, Brita T1 - Holzmodifikation durch Tränkung mit Nanopartikeln T2 - Tagung "Rosenheimer Fenstertage 2004" CY - Rosenheim, Deutschland DA - 2004-01-01 KW - Holzmodifikation KW - Sol-Gel KW - Tränkverfahren KW - Holzschutz PY - 2004 SP - 23 EP - 26 PB - Institut für Fenstertechnik CY - Rosenheim AN - OPUS4-4487 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Böcker, Wolfgang D. G. A1 - Bücker, Michael A1 - Reinsch, Stefan A1 - Unger, Brita T1 - Holzverbundwerkstoffe mit verbesserten Eigenschaften N2 - Die offenporige Struktur des Holzes und dessen chemische Zusammensetzung bieten sich an, über Tränkverfahren geeignete Precursoren so an den inneren Oberflächen des Holzes zu fixieren, dass bei anschließender thermischer Behandlung ein umweltfreundlicher anorganisch-organischer Verbundwerkstoff entsteht. Aus der Literatur sind hierzu verschiedene Ansätze bekannt. - Ziel der vorliegenden Arbeit sind Verbesserungen der biologischen Beständigkeit, der Feuchtebeständigkeit unter Beibehaltung bzw. leichter Verbesserung der mechanischen Eigenschaften des Holzes. Dies wird durch eine chemische Verbindung (Haftung) zwischen den verbundbildenden Phasen Holz und Precursor und eventuell zusätzlichen Einbau von funktionellen organischen Gruppen realisiert. Als Precursoren dienen über den Sol-Gel Weg hergestellte Kieselsole, die nach vollständiger thermischer Umsetzung zu rein anorganischen Phasen (SiO2) führen. Die Sol-Gel Synthese konnte so optimiert werden, dass durch die Behandlung eine homogene Beschichtung aller Oberflächen erreicht werden kann. T2 - Integrierter Umweltschutz im Bereich der Holzwirtschaft CY - Göttingen, Deutschland DA - 2002-01-22 PY - 2002 SP - 100 EP - 102 PB - DGfH CY - München AN - OPUS4-1366 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Welter, T. A1 - Marzok, Ulrich A1 - Deubener, J. A1 - Reinsch, Stefan A1 - Müller, Ralf T1 - Hydrogen diffusivity in sodium aluminosilicate glasses N2 - Hydrogen gas diffusivity of fourteen glasses of the Na2O-Al2O3-SiO2 system are studied along the joins quartzalbite-jadeite-nepheline (Qz-Ab-Jd-Np, fully polymerized) and albite-sodium disilicate (Ab-Ds, depolymerized). Density measurements show that ionic porosity decreases from 54.4% (Qz) to 51.5% (Np) and from 52.4% (Ab) to 50.2% (Ds). Hydrogen diffusivity D follows similar trends but at another scale. D at 523 K decreases from 4×10−12 to 3×10−14m2 s−1 (Qz-Np) and from 4×10−13 to 3×10−15m2 s−1 (Ab-Ds). Charge compensating Na+ acting as a filling agent in fully polymerized network structures leads to up to one order of Magnitude higher diffusivities as depolymerized glass structures of the same SiO2 content where Na+ takes the role of a modifier ion. Temperature dependence of the diffusivity indicates that both the activation energy involved with the moving H2 molecule as well as the accessible volume in the structure contribute to this compositional trend. KW - Aluminosilicate glasses KW - Hydrogen diffusivity KW - Ionic porosity PY - 2019 U6 - https://doi.org/10.1016/j.jnoncrysol.2019.119502 VL - 521 SP - 119502 PB - Elsevier B.V. AN - OPUS4-50392 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Reinsch, Stefan A1 - Welter, T. A1 - Müller, Ralf A1 - Deubener, J. T1 - Hydrogen Permeability of Tectosilicate Glasses for Tank Barrier Liners N2 - The permeation of hydrogen gas was studied in meta-aluminous (tectosilicate) glass powders of Li2O×Al2O3×SiO2 (LAS), Na2O×Al2O3×SiO2 (NAS) and MgO×Al2O3×SiO2 (MAS) systems by pressure loading and vacuum extraction in the temperatures range 210–310 °C. With this method, both the solubility S and the diffusivity D were determined, while the permeability was given by the product SD. For all glasses, S was found to decrease with temperature, while D increased. Since the activation energy of diffusion of H2 molecules exceeded that of dissolution, permeation increased slightly with temperature. When extrapolated to standard conditions (25 °C), the permeability of tectosilicate glasses was found to be only 10-22–10-24 mol H2 (m s Pa)-1, which is 8–10 magnitudes lower than most polymers. Thin glass liners of these compositions are expected to be the most effective barrier for tanks of pressurised hydrogen. KW - Hydrogen permeation KW - Aluminosilicate glasses KW - Hydrogen storage tank KW - Glass liner PY - 2023 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:b43-587284 VL - 1 SP - 1 EP - 11 AN - OPUS4-58728 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Welter, T. A1 - Müller, Ralf A1 - Deubener, J. A1 - Marzok, Ulrich A1 - Reinsch, Stefan T1 - Hydrogen Permeation Through Glass N2 - Physical storage of gaseous hydrogen under high-pressure in glassy micro-containers such as spheres and capillaries is a promising concept for enhancing safety and the volumetric capacity of mobile hydrogen storage systems. As very low permeation through the container wall is required for storage of compressed hydrogen, development of glasses of minimal hydrogen permeability is needed. For this purpose, one has to understand better the dependence of hydrogen permeability on glass structure. The paper points out that minimizing the accessible free volume is as one strategy to minimize hydrogen permeability. Based on previously measured and comprehensive literature data, it is shown that permeation is independently controlled by ionic porosity and network modifier content. Thus, ionic porosity in modified and fully polymerized networks can be decreased equally to the lowest hydrogen permeability among the glasses under study. Applying this concept, a drop of up to 30,000 with respect to the permeation of hydrogen molecules through silica glass is attainable. KW - Ionic porosity KW - hydrogen storage KW - Glass KW - Permeability KW - Solubility KW - Diffusivity PY - 2020 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:b43-513927 VL - 6 SP - Article 342 AN - OPUS4-51392 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Emmerling, Franziska A1 - Villajos Collado, José Antonio A1 - Jagorel, Noëmie A1 - Reinsch, Stefan T1 - Increasing Exposed Metal Site Accessibility in a Co-MOF-74 Material With Induced Structure-Defects N2 - Metal-organic frameworks (MOFs) are promising nanoporous materials with many practical applications. This owes largely to their remarkable porosity and the presence of specific chemical functionalities, such as exposed metal sites (EMS). The MOF-74 structure is known for exhibiting one of the highest EMS densities among porous materials. Moreover, the inclusion of structural defects has been proposed to enhance activity further. This was previously achieved by mixing the original linker together with a second one, having lower topology. The presence of structural defects was evidenced by the resulting crystalline properties and thermal stability. In this work, different mixtures of tetratopic 2,5-dihydroxyterephthalic acid with up to 60% of the tritopic hydroxyterephtalic acid were used to synthesize crystalline Co-MOF-74-like materials. Materials synthesized from higher proportions than 30% of hydroxyterephtalic acid in the synthesis media collapse upon partial removal of the solvent molecules. This indicates the presence of structural defects and the importance of the solvent molecules in stabilizing the crystalline structures. Electron microscope images show that crystal size reduces with inclusion of hydroxyterephtalic acid as the second linker. The presence of coordinated solvent molecules at the EMS was evaluated by Fourier-transform infrared spectra (FTIR) spectroscopy, so that a higher degree of solvent-exchange was observed during washing for defective structures. Furthermore, TG analysis suggests defective structures exhibit lower desolvation temperatures than the defect-free structures. Finally, N2 adsorption-desorption analyses at −196°C showed an enhanced accessibility of the gas to the inner porosity of the defective structures and therefore, the EMS of the material. All these finding make this pathway interesting to enhance the potential interest of these materials for an industrial application because of both a facilitated activation and a better access to the active sites. KW - MOF-74 KW - Structural defects KW - Mixed-linkers KW - Exposed metal sites KW - Facilitated activation PY - 2019 U6 - https://doi.org/10.3389/fmats.2019.00230 VL - 6 SP - 230 PB - Frontiers Media CY - Lausanne AN - OPUS4-49256 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Abel, Andreas A1 - Rosalie, Julian M. A1 - Reinsch, Stefan A1 - Zapala, Pawel A1 - Michels, Heiner A1 - Skrotzki, Birgit T1 - Influence of Mo and B additions in intermetallic near-Fe3Al alloys on microstructure and mechanical properties N2 - Iron aluminides, already reported in the late 19th century, did not cease to attract the interest of scientists and engineers ever since. Besides good oxidation resistance, low density and resource availability, potentials for hightemperature strengths that compete with high-alloy steels were unlocked by low alloy contents. Still, research on alloy design continues, as alloying usually comes at the price of brittleness in low-temperature regimes. A potential candidate is the quinary Fe–Al–Mo–Ti–B system which is strengthened by solid solution and eutectic borides. It was shown to have good strength and outstanding creep resistance under compressive loading up to elevated temperatures. Although the individual effect of alloy additions is well understood in iron aluminides, little is known about the combined effects of alloying concentrations on microstructure, phase stability and mechanical properties. Therefore a systematic study of two Ti-doped near-Fe3Al alloys with varying contents of Mo (2–4 at.%) and B (0.5–1 at.%) was conducted. In total eight different alloys were fabricated by investment casting into ceramic shell molds. Alloys were characterized and compared by grain size, phase transitions, microstructure evolution as well as elemental compositions and volume fractions of phases. For mechanical characterization, macrohardness and microhardness tests as well as tensile tests at ambient and high tempera tures were conducted. Independent of alloy additions, alloys with 24–25 at.% Al exhibit superior proof strength due to a higher matrix hardness. Decreasing B content generally decreases strength by lower secondary phase fractions which contribute via particle hardening. Reducing Mo content decreases both the solute concentration in the matrix and secondary phase fractions. Surprisingly, strength is similar or even superior to alloys with higher Mo content. Strength relations are discussed with a focus on solid-solution hardening theory and other competing strengthening mechanisms. KW - Materials Chemistry KW - Metals and Alloys KW - Mechanical Engineering KW - Mechanics of Materials KW - General Chemistry PY - 2023 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:b43-585284 VL - 163 SP - 1 EP - 11 PB - Elsevier Ltd. AN - OPUS4-58528 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Deubener, J. A1 - Behrens, H. T1 - Internal friction of hydrated soda-lime-silicate glasses N2 - The internal friction of hydrated soda-lime-silica glasses with total water content (CW ) up to 1.9 wt. % was studied by dynamic mechanical analysis (DMA) using temperature-frequency sweeps from 723 K to 273 K and from 1 s-1 to 50 s-1. Total water content and concentrations of H2O molecules (CH2O ) and OH groups (COH) in the DMA specimens were determined by infrared spectroscopy. For low water contents (CW ≈ COH < 0.25 wt. %) two discrete internal friction peaks below the glass transition (α relaxation) were assigned to the low-temperature motion of alkali ions (γ relaxation) and cooperative movements of dissimilar mobile species under participation of OH at higher temperature (βOH relaxation). For large water contents (CW > 1 wt. %), where significant amounts of molecular water are evident (CH2O > 0.15 wt. %), however, internal friction spectra change unexpectedly: the βOH peak heights saturate and a low temperature shoulder appears on the β-relaxation peak. This emerging relaxation mode (βH2O relaxation) was assigned to the motions of H2O molecules. βH2O relaxation was found to be faster than βOH but slower than γ relaxation. Activation energy of the different relaxation modes increased in the order γ < βH2O < βOH < α. KW - Internal friction KW - Glass KW - Water content PY - 2013 U6 - https://doi.org/10.1063/1.4828740 SN - 0021-9606 SN - 1089-7690 VL - 139 SP - 174506-1 EP - 174506-6 PB - American Institute of Physics CY - Melville, NY AN - OPUS4-29698 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Tielemann, Christopher A1 - Reinsch, Stefan A1 - Maaß, Robert A1 - Deubener, J. A1 - Müller, Ralf T1 - Internal nucleation tendency and crystal surface energy obtained from bond energies and crystal lattice data N2 - We present an easy-to-apply method to predict structural trends in the internal nucleation tendency of oxide glasses. The approach is based on calculated crystal fracture surface energies derived from easily accessible diatomic bond energy and crystal lattice data. The applicability of the method is demonstrated on literature nucleation data for isochemically crystallizing oxide glasses. KW - Glass KW - Nucleation tendency KW - Fracture surface energy KW - Crystal lattice KW - Bond energy PY - 2022 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:b43-548814 SN - 2590-1591 VL - 14 SP - 1 EP - 5 PB - Elsevier B.V. AN - OPUS4-54881 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -