TY - CONF A1 - de Moraes, Flavia A1 - Frischat, G. H. A1 - Heide, G. A1 - Müller, Wolfgang A1 - Müller, Ralf T1 - Korrosions- und Kristallisationsphänomene an der Innenoberfläche von Glasbausteinen T2 - 77. Glastechnische Tagung CY - Leipzig, Deutschland DA - 2003-05-26 PY - 2003 VL - 77 SP - 71 EP - 74 PB - DGG CY - Offenbach AN - OPUS4-2527 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Weh, Lothar A1 - Müller, Ralf A1 - Moseler, D. A1 - Heide, G. A1 - Frischat, G. T1 - Topographische Untersuchungen von Glasoberflächen mit Vickers-Eindrücken T2 - 74. Glastechnische Tagung CY - Ulm, Deutschland DA - 2000-05-29 PY - 2000 SP - 237 EP - 240 PB - DGG, Dt. Glastechn. Ges. CY - Frankfurt/M. AN - OPUS4-934 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - de Moraes, Flavia A1 - Müller, Wolfgang A1 - Frischat, G.H. A1 - Müller, Ralf T1 - Corrosion and crystallization at the inner surfaces of glass bricks N2 - Glass bricks are important transparent building materials. They are produced by joining two halves of glass pressings at 600–700 °C. During this production process alkali oxides evaporate and are redeposited at the cooler inner front surfaces of the bricks. This surface layer reacts with H2O and CO2 from the residual brick atmosphere, leading to the formation of an alkali-rich silicate-hydrate layer of ≥50 nm thickness, which could be evidenced leading to a reduced nano-hardness of similar thickness, and from which NaHCO3 crystals can finally grow. Climate chamber experiments (repeated cooling between at -8 and -14 °C and reheating to 0 to 15 °C) resulted in reversible NaHCO3 crystallization and redissolution, presumably influenced by water evaporation or condensation and driven by the NaHCO3 supersaturation of the silicate-hydrate layer. Depending on the time–temperature schedule, different crystal morphologies became visible in this closed system, e.g. isolated spherical crystals, crystals arranged in chains and in double-chains, respectively, which can limit already the transmittance of the glass bricks. When a crack occurs or the brick is opened, the hygroscopic NaHCO3 crystals take up more H2O from the ambient, react irreversibly with the glass surface, finally leading to a total loss of transmittance. KW - Chemical properties KW - Chemical durability KW - Corrosion KW - Crystallization KW - Crystal growth KW - Nucleation KW - Glasses KW - Mass spectroscopy KW - Mechanical properties KW - Hardness KW - Indentation KW - Microindentation KW - Microscopy KW - Optical microscopy KW - Scanning electron microscopy KW - Optical properties KW - Optical spectroscopy KW - Oxide glasses KW - Alkali silicates KW - Soda-lime-silica KW - Surfaces and interfaces PY - 2008 DO - https://doi.org/10.1016/j.jnoncrysol.2007.07.086 SN - 0022-3093 VL - 354 IS - 2-9 SP - 284 EP - 289 PB - North-Holland Publ. Co. CY - Amsterdam AN - OPUS4-16433 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Altantsog, Pagvajav A1 - Ojunbileg, L. A1 - Tserenshimed, M. A1 - Chadraabal, Shgdariin A1 - Müller, Ralf A1 - Nofz, Marianne A1 - Gaber, Martin A1 - Batdemberel, G. A1 - Sangaa, D. T1 - Some experimental results of glass melting by using sands from Buir nuur PY - 2002 VL - 1 SP - 103 EP - 118 AN - OPUS4-3113 LA - mon AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Deubener, Joachim A1 - Müller, Ralf A1 - Behrens, H. A1 - Heide, G. T1 - Water and the glass transition temperature of silicate melts N2 - Literature data on the effect of water on the glass transition in silicate melts are gathered for a broad range of total water content cw from 3 × 10-4 to 27 wt%. In terms of a reduced glass transition temperature Tg*=Tg/TgGN, where TgGN is Tg of the melt containing cw?0.02 wt% total water, a uniform dependence of Tg* on total water content (cw) is evident for silicate melts. Tg* decreases steadily with increasing water content, most strongly at the lowest water content where H2O is dominantly dissolved as OH. For water-rich melts, the variation of Tg* is less pronounced, but it does not vanish even at the largest water contents reported (?27 wt%). Tg* vs. cw is fitted by a three-component model. This approach accounts for different transition temperatures of the dry glass, hydroxyl and molecular water predicting Tg* as a weighted linear combination of these temperatures. The required but mostly unknown water speciation in the glasses was estimated using IR-spectroscopy data for hydrous sodium trisilicate and rhyolite. PY - 2003 DO - https://doi.org/10.1016/S0022-3093(03)00472-1 SN - 0022-3093 VL - 330 SP - 268 EP - 273 PB - North-Holland Publ. Co. CY - Amsterdam AN - OPUS4-3120 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Blaeß, Carsten A1 - Müller, Ralf A1 - Poologasundarampilai, G. A1 - Brauer, D. S. T1 - Sintering and concomitant crystallization of bioactive glasses N2 - The sintering of bioactive glasses allows for the preparation of complex structures, such as three‐dimensional porous scaffolds. Such 3D constructs are particularly interesting for clinical applications of bioactive glasses in bone regeneration, as the scaffolds can act as a guide for in‐growing bone cells, allowing for good Integration with existing and newly formed tissue while the scaffold slowly degrades. Owing to the pronounced tendency of many bioactive glasses to crystallize upon heat treatment, 3D scaffolds have not been much exploited commercially. Here, we investigate the influence of crystallization on the sintering behavior of several bioactive glasses. In a series of mixed‐alkali glasses an increased CaO/alkali metal oxide Ratio improved sintering compared to Bioglass 45S5, where dense sintering was inhibited. Addition of small amounts of calcium fluoride helped to keep melting and sintering temperatures low. Unlike glass 13‐93, these new glasses crystallized during sintering but this did not prevent densification. Variation in bioactive glass particle size allowed for fine‐tuning the microporosity resulting from the sintering process. KW - Bioactive glass KW - Crystallization KW - Scaffolds KW - Sintering PY - 2019 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-485458 DO - https://doi.org/10.1111/ijag.13477 SN - 2041-1286 VL - 10 IS - 4 SP - 449 EP - 462 PB - Wiley AN - OPUS4-48545 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wirth, Cynthia A1 - Müller, Ralf A1 - Günster, Jens A1 - Mühler, T. A1 - Görke, R. A1 - Heinrich, J.G. T1 - Submicrometer silica spheres generated by laser fuming N2 - The production of agglomerate-free SiO2 particles exhibiting a monomodal distribution of particle sizes of around 300 nm by means of direct laser fuming of micrometric SiO2 powders has been successfully demonstrated. With a 12 kW cw CO2 laser system, a production rate of up to 1 kilogram powder per hour was achieved. Almost ideal spherical amorphous SiO2 particles in a broad particle size distribution between 10 nm and several 100 nm (d50 ≈ 300 nm) were synthesized. Several observations suggest weak agglomeration forces between the particles. A temperature reduction of 200 °C for sintering powder compacts was observed. KW - Laser KW - SiO2 KW - Nanopowder PY - 2013 DO - https://doi.org/10.4416/JCST2012-00033 SN - 2190-9385 N1 - Geburtsname von Wirth, Cynthia: Gomes, C. M. - Birth name of Wirth, Cynthia: Gomes, C. M. VL - 4 IS - 1 SP - 11 EP - 18 PB - Göller CY - Baden-Baden AN - OPUS4-31423 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -