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 DO - 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 - CONF A1 - Eberstein, Markus A1 - Müller, Ralf A1 - Reinsch, Stefan A1 - Rabe, Torsten A1 - Schiller, Wolfgang Arno A1 - Thiel, A. A1 - Deubener, J. T1 - Kinetic Modeling of LTCC-Shrinkage T2 - 3rd International Conference and Exhibition on Ceramic Interconnect and Ceramic Microsystems Technologies (CICMT 2007) CY - Denver, CO, USA DA - 2007-04-23 KW - LTCC KW - Glass matrix composites KW - Inclusions KW - Sintering kinetics KW - Modeling PY - 2007 SP - 1 EP - 8 PB - American Ceramic Soc. CY - Denver AN - OPUS4-14948 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Eberstein, Markus A1 - Müller, Ralf A1 - Reinsch, Stefan A1 - Rabe, Torsten A1 - Schiller, Wolfgang Arno A1 - Thiel, A. A1 - Deubener, J. T1 - Kinetic Modeling of LTCC Shrinkage: Effect of Alumina Content N2 - We studied sintering of LTCC-type glass matrix composites (GMCs) consisting of small glass and alumina particles of equal size. Primarily, crystals act as rigid inclusions, decelerating the densification rate. In later stages, they also dissolve, partially increasing the viscosity. Release of alumina finally induces crystallization of alumosilicates, which enables post-firing stability. To study both effects, two model GMCs were prepared: an α-Al2O3 + barium alumoborosilicate glass (BABS)–GMC, which shows neither significant dissolution nor crystallization, and an α-Al2O3 + calcium alumoborosilicate glass (CABS)–GMC, which dissolves readily and promotes crystallization. The kinetics of shrinkage for both GMC were modeled by utilizing Frenkel theory for the early stage and Mackenzie–Shuttleworth theory for the late stage, assuming that sintering is superimposed by the weighted contributions of triparticle glass–crystal clusters, their random occurrence (ideal mixing), and a shrinkage rate controlled by the GMC effective viscosity. In agreement with modeling, the experimental results showed that the shrinkage rate of BABS–GMC decreases progressively for crystal volume fractions Φ > 0.15. The attainable shrinkage is reduced by up to 8% for Φ = 0.45. For the CABS–GMC with Φ = 0.25, a reduction of Φ to 0.20 was evident due to partial α-Al2O3 dissolution. This effect was found able to increase the sintering temperature by ~50–60 K. KW - LTCC KW - Glas Matrix Composites KW - Inclusions KW - Sintering Kinetics KW - Modeling PY - 2007 SN - 1551-4897 VL - 4 IS - 4 SP - 173 EP - 180 CY - Washington, DC AN - OPUS4-16506 LA - eng 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 - 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 - 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 DO - 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 - 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 - 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 DO - 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 - GEN A1 - Reinsch, Stefan A1 - Meng, S. A1 - Eberstein, Markus A1 - Thiel, A. A1 - Müller, Ralf A1 - Deubener, J. T1 - Partial Solution of Dispersed alpha-Al2O3-Particles in Alumoborosilicate Glass T2 - 81. Glastechnische Tagung CY - Aachen, Deutschland DA - 2007-06-04 KW - Glasmatrixkomposite KW - Lösung KW - Sintern PY - 2007 SN - 978-3-921089-52-1 IS - CD-ROM SP - 1 EP - 5 PB - Deutsche Glastechnische Gesellschaft CY - Offenbach AN - OPUS4-16108 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Reinsch, Stefan A1 - Gaber, Martin A1 - Müller, Ralf A1 - Schiller, Wolfgang Arno T1 - Rate controlled debindering of glass ceramic composites N2 - Green compacts of ceramics, glass ceramic composites and sinter glass ceramics contain different amounts of organic materials added as pressing aids or binders. Before sintering, these organics have to burn out completely. In oxidising atmospheres, the debindering process is mostly exothermic and therefore difficult to control. This uncontrolled heat production due to locally enhanced debindering and respective gas release may cause damages in the green compact microstructure. Therefore, debindering is usually operated with very low heating rates (< 3 K/min) which requires long processing times of many hours. In this paper, we will show that it is possible to reduce the processing time for debindering dramatically by using the decomposition rate of the organic binder, detected by the weight loss of the sample, as a control factor of the furnace. T2 - 9th ESG (European Society of Glass) Conference with the Annual Meeting of the ICG Glass - "The challenge for the 21st century" CY - Trencin, Slovakia DA - 2008-06-22 KW - Debindering KW - Thermo gravimetry KW - Glass ceramic composites PY - 2005 SN - 1022-6680 SN - 1662-8985 VL - 39-40 SP - 583 EP - 586 PB - Trans Tech Publ. CY - Zurich AN - OPUS4-17840 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Deubener, J. A1 - Behrens, H. A1 - Müller, Ralf A1 - Zietka, S. A1 - Reinsch, Stefan T1 - Kinetic fragility of hydrous soda-lime-silica glasses N2 - The effect of hydration on the kinetic fragility of soda-lime-silica glasses was investigated by viscometry in the glass transition range. Water-bearing glasses were prepared from industrial float glass (FG) and a ternary model glass (NCS = 16Na2O 10CaO 74SiO2 in mol%) by bubbling steam through the melt at 1480 °C and up to 7 bar. Additionally, a sodium borosilicate glass (NBS = 16Na2O 10B2O3 74SiO2 in mol%) was hydrated under equal conditions. As detected by infrared spectroscopy water dissolves in the glasses exclusively as OH-groups. The hydration resulted in a total water content CW up to ~ 0.2 wt% for FG, NCS and NBS glasses. Kinetic fragility, expressed by the steepness index m, was determined from the temperature dependence of η at the glass transition. Viscosity data from previous studies on hydrous float glasses (CW > 1 wt%) were surveyed together with literature data on the (H2O)–Na2O–CaO–SiO2, (H2O)–Na2O–SiO2 and (H2O)–SiO2 systems to expand the range of water concentration and bulk composition. We could demonstrate that m decreases for all glasses although water is dissolved as OH and should depolymerize the network. An empirical equation of the general type m = a - b logCW where a, b are fitting parameters, enables m to be predicted, for each glass series as function of the water content CW. The enlarged data base shows that the parameter B of the Arrhenius viscosity-temperature relation decreases much stronger than the isokom temperature at the glass transition. KW - Soda-lime-silica KW - Fragility KW - Viscosity KW - Water in glass PY - 2008 DO - https://doi.org/10.1016/j.jnoncrysol.2008.04.021 SN - 0022-3093 VL - 354 IS - 42-44 SP - 4713 EP - 4718 PB - North-Holland Publ. Co. CY - Amsterdam AN - OPUS4-18187 LA - eng 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 DO - 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 - JOUR A1 - Winkel, A. A1 - Meszaros, R. A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Travitzky, N. A1 - Fey, T. A1 - Greil, P. A1 - Wondraczek, L. T1 - Sintering of 3D-printed glass/HAp composites N2 - We report the sintering of 3D-printed composites of 13-93 bioactive glass and hydroxyapatite (HAp) powders. The sintering process is characterized on conventionally produced powder compacts with varying HAp content. A numeric approximation of the densification kinetics is then obtained on the basis of Frenkel, Mackenzie–Shuttleworth, and Einstein–Roscoe models, and optimized sintering conditions for 3D-printed structures are derived. Fully isotropic sintering of complex cellular composites is obtained by continuous heating to 750°C at a rate of 2 K/min for a HAp content of 40 wt%. The approach can readily be generalized for printing and sintering of similar glass-ceramic composites. KW - Sintering glass composit bio material PY - 2012 DO - https://doi.org/10.1111/j.1551-2916.2012.05368.x SN - 0002-7820 SN - 1551-2916 VL - 95 IS - 11 SP - 3387 EP - 3393 PB - Blackwell Publishing CY - Malden AN - OPUS4-27053 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Müller, Ralf A1 - Reinsch, Stefan ED - Bansal, N. P. ED - Boccaccini, A.R. T1 - Viscous-phase silicate processing KW - Viskoses Sintern KW - Oberflächenkeimbildung KW - Glaspulver KW - Sintermodelle KW - Sinterglaskeramik KW - Glasmatrixkomposit PY - 2012 SN - 978-0-470-55344-2 IS - Chapter 3 SP - 75 EP - 144 PB - Wiley AN - OPUS4-27054 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 DO - 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 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-548814 DO - https://doi.org/10.1016/j.nocx.2022.100093 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 - TY - CONF A1 - Reinsch, Stefan A1 - Tielemann, Christopher A1 - Müller, Ralf A1 - Busch, R. A1 - Patzig, C. A1 - Höche, T. T1 - Surface-Initiated Microstructure Formation in Glass Ceramics N2 - Up to now, oriented surface crystallization phenomena are discussed controversially, and related studies are restricted to few glasses. For silicate glasses we found a good correlation between the calculated surface energy of crystal faces and oriented surface nucleation. Surface energies were estimated assuming that crystal surfaces resemble minimum energy crack paths along the given crystal plane. This concept was successfully applied by Rouxel in calculating fracture surface energies of glasses. Several oriented nucleation phenomena can be herby explained assuming that high energy crystal surfaces tend to be wetted by the melt. This would minimize the total interfacial energy of the nucleus. Furthermore, we will discuss the evolution of the microstructure and its effect on the preferred crystal orientation. T2 - 26th International Congress on Glass CY - Berlin, Germany DA - 03.07.2022 KW - Glass KW - Oriented surface crystallization KW - Surface energy KW - Bond energy KW - Nucleation mode PY - 2022 AN - OPUS4-56070 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Tielemann, Christopher A1 - Busch, R. A1 - Reinsch, Stefan A1 - Patzig, C. A1 - Höche, T. A1 - Avramov, I. A1 - Müller, Ralf T1 - Oriented surface nucleation in diopside glass N2 - Es wird die Texturbildung in kristallisierendem Diopsidglas im Zusammenhang mit der Oberflächenbeschaffenheit der unbehandelten Probe untersucht. Zudem wird der diskutiert, dass es sich bei der Texturbildung in Gläsern höchstwahrscheinlich um ein Nukleationsphänomen handelt welches auf die richtungsabhängige Grenzflächenenergie der kristallisierenden Phase zurückzuführen ist. N2 - Oriented surface crystallization on polished diopside glass surfaces has been studied with scanning electron microscopy, electron backscatter diffraction, transmission electron microscopy and laser scanning microscopy. An orientation preference of [001] parallel to the glass surface was detected for separately growing diopside crystals even as small as 700 nm in size. This finding shows that crystal orientation occurs in the outermost surface layer without crystal-crystal interaction and indicates that the crystal orientation is a result of oriented nucleation. Depending on surface preparation, monomodal crystal orientation distributions with [100] perpendicular to the surface or bimodal distributions with [100] and [010] perpendicular to the glass Surface were detected. It was also shown that the degree of crystal orientation increases with decreasing Surface roughness. The observed orientation of diopside crystals could be explained in terms of the interfacial energies of different crystal faces. KW - Surface energy KW - Glass ceramic KW - Glass KW - EBSD KW - Diopsid PY - 2021 UR - https://www.sciencedirect.com/science/article/pii/S002230932100020X DO - https://doi.org/10.1016/j.jnoncrysol.2021.120661 SN - 0022-3093 VL - 562 PB - Elsevier B.V. AN - OPUS4-53073 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Busch, R. A1 - Tielemann, Christopher A1 - Reinsch, Stefan A1 - Müller, Ralf A1 - Patzig, C. A1 - Krause, M. A1 - Höche, T. T1 - Sample preparation for analytical scanning electron microscopy using initial notch sectioning N2 - A novel method for broad ion beam based sample sectioning using the concept of initial notches is presented. An adapted sample geometry is utilized in order to create terraces with a well-define d step in erosion depth from the surface. The method consists of milling a notch into the surface, followed by glancing-angle ion beam erosion, which leads to preferential erosion at the notch due to increased local surface elevation. The process of terrace formation can be utilized in sample preparation for analytical scanning electron microscopy in order to get efficient access to the depth-dependent microstructure of a material. It is demonstrated that the method can be applied to both conducting and non-conducting specimens. Furthermore, experimental parameters influencing the preparation success are determined. Finally, as a proof-of-concept, an electron backscatter diffraction study on a surface crystallized diopside glass ceramic is performed, where the method is used to analyze orientation dependent crystal growth phenomena occurring during growth of surface crystals into the bulk. KW - 3D etching KW - Ion beam erosion Sectioning KW - EBSD KW - Sample preparation KW - Analytical scanning electron microscopy KW - SEM KW - Glass Ceramic KW - Glass KW - Diopsid PY - 2021 DO - https://doi.org/10.1016/j.micron.2021.103090 SN - 0968-4328 VL - 150 PB - Elsevier B.V. AN - OPUS4-53075 LA - eng 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 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-531227 DO - https://doi.org/10.1002/adem.202100445 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 -