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 - JOUR A1 - Schneider, J. A1 - Farris, L. A1 - Nolze, Gert A1 - Reinsch, Stefan A1 - Cios, G. A1 - Tokarski, T. A1 - Thompson, S. T1 - Microstructure evolution in Inconel 718 produced by powder bed fusion additive manufacturing N2 - Inconel 718 is a precipitation strengthened, nickel-based super alloy of interest for the Additive Manufacturing (AM) of low volume, complex parts to reduce production time and cost compared to conventional subtractive processes. The AM process involves repeated rapid melting, solidification and reheating, which exposes the material to non-equilibrium conditions that affect elemental segregation and the subsequent formation of solidification phases, either beneficial or detrimental. These variations are difficult to characterize due to the small length scale within the micron sized melt pool. To understand how the non-equilibrium conditions affect the initial solidification phases and their critical temperatures, a multi-length scale, multi modal approach has been taken to evaluate various methods for identifying the initial phases formed in the as-built Inconel 718 produced by laser-powder bed fusion (L-PBF) additive manufacturing (AM). Using a range of characterization tools from the bulk differential thermal analysis (DTA) and x-ray diffraction (XRD) to spatially resolved images using a variety of electron microscopy tools, a better understanding is obtained of how these minor phases can be properly identified regarding the amount and size, morphology and distribution. Using the most promising characterization techniques for investigation of the as-built specimens, those techniques were used to evaluate the specimens after various heat treatments. During the sequence of heat treatments, the initial as-built dendritic structures recrystallized into well-defined grains whose size was dependent on the temperature. Although the resulting strength was similar in all heat treated specimens, the elongation increased as the grain size was refined due to differences in the precipitated phase distribution and morphology. KW - Metal additive manufacturing KW - Inconel 718 KW - Heat treatment KW - Grain boundary precipitates KW - Laves phase PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-542758 DO - https://doi.org/10.3390/jmmp6010020 SN - 2504-4494 VL - 6 IS - 1 SP - 1 EP - 20 PB - MDPI CY - Basel AN - OPUS4-54275 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Paskin, A. A1 - Couasnon, T. A1 - Perez, J. P. H. A1 - Lobanov, S. S. A1 - Blukis, R. A1 - Reinsch, Stefan A1 - Benning, L. G. T1 - Nucleation and Crystallization of Ferrous Phosphate Hydrate via an Amorphous Intermediate N2 - The fundamental processes of nucleation and crystallization are widely observed in systems relevant to material synthesis and biomineralization; yet most often, their mechanism remains unclear. In this study, we unravel the discrete stages of nucleation and crystallization of Fe3(PO4)2·8H2O (vivianite). We experimentally monitored the formation and transformation from ions to solid products by employing correlated, time-resolved in situ and ex situ approaches. We show that vivianite crystallization occurs in distinct stages via a transient amorphous precursor phase. The metastable amorphous ferrous phosphate (AFEP) intermediate could be isolated and stabilized. We resolved the differences in bonding environments, structure, and symmetric changes of the Fe site during the transformation of AFEP to crystalline vivianite through synchrotron X-ray absorption spectroscopy at the Fe K-edge. This intermediate AFEP phase has a lower water content and less distorted local symmetry, compared to the crystalline end product vivianite. Our combined results indicate that a nonclassical, hydration-induced nucleation and transformation driven by the incorporation and rearrangement of water molecules and ions (Fe2+ and PO4 3−) within the AFEP is the dominating mechanism of vivianite formation at moderately high to low vivianite supersaturations (saturation index ≤ 10.19). We offer fundamental insights into the aqueous, amorphous-to-crystalline transformations in the Fe2+−PO4 system and highlight the different attributes of the AFEP, compared to its crystalline counterpart. KW - Nucleation KW - Crystallization KW - Vivianite KW - Ferrous phosphate hydrate PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-580696 DO - https://doi.org/10.1021/jacs.3c01494 SN - 0002-7863 VL - 145 IS - 28 SP - 15137 EP - 15151 PB - ACS Publications AN - OPUS4-58069 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ivanov, V.V. A1 - Tielemann, Christopher A1 - Avramova, K. A1 - Reinsch, Stefan A1 - Tonchev, V. T1 - Modelling crystallization: When the normal growth velocity depends on the supersaturation N2 - The crystallization proceeds by the advance of the crystal faces into the disordered phase at the expense of the material excess, the supersaturation. Using a conservation constraint for the transformation ratio α∈[0,1] as complementing the rescaled supersaturation to 1 and a kinetic law for the normal growth velocity as function of the supersaturation raised to power g, the growth order, we derive an equation for the rate of transformation dα/dt. We integrate it for the six combinations of the three spatial dimensions D = 1, 2, 3 and the two canonical values of g = 1, 2 towards obtaining expressions for αDg. The same equation, with g = 1 and D = n (n is the so called Avrami exponent) is obtained when taking only the linear in α term from the Taylor’s expansion around α = 0 of the model equation of Johnson-Mehl-Avrami-Kolmogorov (JMAK). We verify our model by fitting datasets of α21 and α31 (from α = 0 to αupper = 0.999) with JMAK to obtain from the fit n = 1.725, 2.43, resp. We show further how the values of n depend on the value of αupper to which the fit is performed starting always from 0. Towards building a validation protocol, we start with validating α21 with published results. KW - Crystallization KW - Supersaturation KW - Growth kinetics KW - Growth rate KW - JMAK model PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-581706 DO - https://doi.org/10.1016/j.jpcs.2023.111542 SN - 0022-3697 VL - 181 SP - 1 EP - 10 PB - Elsevier Ltd. AN - OPUS4-58170 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Patzig, C. T1 - Surface-initiated microstructure formation in glass ceramics N2 - Up to now, the mechanisms of surface nucleation and surface-induced texture formation are far from being understood. Corresponding phenomena are discussed hypothetically or even controversial, and related studies are restricted to very few glasses. As a main drawback, the vast majority of previous work on oriented growth of surface crystals do not consider the possible effects of glass surface treatments (like polishing defects, adhered particles and cracks, …) or ambient annealing conditions (vacuum or atmospheric pressure) which both can influence crystal nucleation and growth. Moreover, very few observations of crystal orientation related to surface crystallization were focused on separately growing crystals. In conclusion, up to now, no systematic studies on initially oriented crystal growth or nucleation from defined active nucleation sites have been pursued. Therefore, the main objective of the proposed project is to gain a basic understanding of the mechanisms of surface-induced microstructure formation in glass ceramics. We shall answer the question whether preferred orientation of surface crystals is the result of oriented nucleation or caused by other orientation selection mechanisms acting during early crystal growth. In both cases, crystal orientation may be caused by the orientation of the glass surface itself or the anisotropy and orientation of active surface nucleation defects. New techniques of experimental characterization of surface-crystallized glasses shall be applied to find answers to the questions posed above. Based on a controlled preparation and annealing of the glass sample surfaces, that includes the defined creation of active nucleation defects, and followed by the microstructural characterization especially during the very early growth stages of separated surface crystals, the orientation relations between defect and initiated surface crystal will be analyzed. In order to gain new insights, a couple of entirely new microstructure diagnostics techniques, including chemically contrasted XRM, laser-based sample preparation for XRM, and 3D electron backscatter diffraction shall be developed or applied. This way, using X-ray microscopy as a pivotal technique for the non-destructive 3D characterization of relatively large samples at superior spatial resolution (but also complemented by other microstructure diagnostics techniques, e.g. TEM elemental mappings at cross-sectioned samples) unprecedented insights into the microstructure evolution upon surface crystallization of model glasses will be gained. T2 - DFG Begutachtungskolloquium (PAK 949/1 und PAK 950/1) CY - Bonn, Germany DA - 07.03.2017 KW - Oberflächenkeimbildung KW - Glaskeramik KW - Orientierung PY - 2017 AN - OPUS4-44219 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan A1 - Patzig, C. T1 - Surface-initiated microstructure formation in glass ceramics N2 - Up to now, the mechanisms of surface nucleation and surface-induced texture formation are far from being understood. Corresponding phenomena are discussed hypothetically or even controversial, and related studies are restricted to very few glasses. As a main drawback, the vast majority of previous work on oriented growth of surface crystals do not consider the possible effects of glass surface treatments (like polishing defects, adhered particles and cracks, …) or ambient annealing conditions (vacuum or atmospheric pressure) which both can influence crystal nucleation and growth. Moreover, very few observations of crystal orientation related to surface crystallization were focused on separately growing crystals. In conclusion, up to now, no systematic studies on initially oriented crystal growth or nucleation from defined active nucleation sites have been pursued. Therefore, the main objective of the proposed project is to gain a basic understanding of the mechanisms of surface-induced microstructure formation in glass ceramics. We shall answer the question whether preferred orientation of surface crystals is the result of oriented nucleation or caused by other orientation selection mechanisms acting during early crystal growth. In both cases, crystal orientation may be caused by the orientation of the glass surface itself or the anisotropy and orientation of active surface nucleation defects. New techniques of experimental characterization of surface-crystallized glasses shall be applied to find answers to the questions posed above. Based on a controlled preparation and annealing of the glass sample surfaces, that includes the defined creation of active nucleation defects, and followed by the microstructural characterization especially during the very early growth stages of separated surface crystals, the orientation relations between defect and initiated surface crystal will be analyzed. In order to gain new insights, a couple of entirely new microstructure diagnostics techniques, including chemically contrasted XRM, laser-based sample preparation for XRM, and 3D electron backscatter diffraction shall be developed or applied. This way, using X-ray microscopy as a pivotal technique for the non-destructive 3D characterization of relatively large samples at superior spatial resolution (but also complemented by other microstructure diagnostics techniques, e.g. TEM elemental mappings at cross-sectioned samples) unprecedented insights into the microstructure evolution upon surface crystallization of model glasses will be gained. T2 - DFG Begutachtungskolloquium (PAK 949/1 und PAK 950/1) CY - Bonn, Germany DA - 07.03.2017 KW - Oberflächenkeimbildung KW - Glaskeramik KW - Orientierung PY - 2017 AN - OPUS4-44221 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Reinsch, Stefan T1 - Surface-induced Crystallization of Glass N2 - Up to now, the mechanisms of surface nucleation and surface-induced texture formation are far from being understood. Corresponding phenomena are discussed hypothetically or even controversial, and related studies are restricted to very few glasses. In this talk the state of the art on mechanisms of surface nucleation are summarized. On one hand, mechanical damaged surfaces show high nucleation activity, at which the nucleation occurs at convex tips and edges preferentially. On the other hand, solid foreign particles are dominant nucleation sites at low damaged surfaces. They enable nucleation at temperatures even far above Tg. The nucleation activity of the particles is substantially controlled by their thermal and chemical durability. But no systematic studies on initially oriented crystal growth or nucleation from defined active nucleation sites have been pursued, so far. Therefore, the main objective of a just started project is to advance the basic understanding of the mechanisms of surface-induced microstructure formation in glass ceramics. We shall answer the question whether preferred orientation of surface crystals is the result of oriented nucleation or caused by other orientation selection mechanisms acting during early crystal growth. In both cases, crystal orientation may be caused by the orientation of the glass surface itself or the anisotropy and orientation of active surface nucleation defects. As a first attempt we focused on possible reorientation of separately growing surface crystals during early crystal growth. First results show clear evidence that separately growing crystals can reorient themselves as they are going to impinge each other. T2 - Glasforum der Deutschen Glastechnischen Gesellschaft (DGG) CY - Würzburg, Germany DA - 11.06.2018 KW - Crystallization KW - Silicate Glasses KW - Surface Nucleation PY - 2018 AN - OPUS4-45593 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Fest, Sarah Ute A1 - Reinsch, Stefan A1 - Müller, Ralf T1 - Milling, sintering and crystallization of 11BaO-25CaO-64SiO2 glass powder N2 - The crystallization of 11BaO-25CaO-64SiO2 mol% glass powders and related effects of glass powder milling have been studied by X-ray diffraction (XRD), light and scanning electron microscopy (SEM) and differential thermal analysis (DTA). Glass powders were made by ZrO2 crushing with subsequent sieving or sedimentation or alternatively made by milling with agate, corundum and tungsten carbide. Although surface crystallization was detectable during late sintering, all powders fully sintered. Wollastonite was found as primary crystal phase followed by cristobalite and sanbornite precipitation. The latter crystallization steps caused a second DTA-peak for fine powders. DTA-peak temperatures shifted to lower temperature with decreasing particle size in any case. No significant effects of milling materials on DTA-peak temperatures were evident. As an exception, however, milling in agate caused strongly decreased temperatures of the second DTA-peak. This observation can be explained by the progressive mechanical damaging, which results from the required prolonged milling time with agate due to its small materials density, and the fact that diamond made scratches did promote surface crystallization of cristobalite. The present study thus shows that even for glass powders with excellent sinterability, milling can affect microstructure evolution. KW - Glass KW - Crystallization KW - Powder preparation KW - SOFC PY - 2014 UR - http://onlinelibrary.wiley.com/doi/10.1111/ijag.12080/full DO - https://doi.org/10.1111/ijag.12080 SN - 2041-1286 SN - 2041-1294 VL - 5 IS - 3 SP - 236 EP - 247 PB - Wiley-Blackwell CY - Hoboken, NJ [u.a.] AN - OPUS4-30807 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bauer, Ute A1 - Behrens, H. A1 - Fechtelkord, M. A1 - Reinsch, Stefan A1 - Deubener, J. T1 - Water- and boron speciation in hydrous soda-lime-borate glasses N2 - The structural investigation of hydrated borate glasses provides new insights on the influence of water on boron speciation using spectroscopic methods. In the present study three soda–lime–borate glasses (NCBx with x = 5, 15 and 25 corresponding to xNa2O, 10CaO, 90 - xB2O3 in mol%) were prepared with water content up to 8 wt.%. The water speciation in the glasses was derived by near-infrared (NIR) spectroscopy while boron speciation was investigated by 11B MAS NMR (Magic Angle Spinning Nuclear Magnetic Resonance). For the three glasses effective molar absorption coefficients were determined experimentally for the bands at 5200 cm- 1 and 4600 cm- 1, corresponding to combination modes of H2O molecules and OH-groups, respectively. In contrast to silicate glasses, in which at most ~ 2 wt.% H2O are dissociated to OH-groups, the amount of dissociated H2O may even exceed 5 wt.% in borate glasses. The fraction of tetrahedral to total boron (N4 = BIV / BIV + BIII) is predominantly controlled by the ratio of Na2O + CaO / B2O3, but only weakly affected by the water content of the glasses. When increasing the H2O content from 0 to 8 wt.%, N4 increases from 25% to 26% for NCB5 and from 42% to 47% for NCB25 glasses. KW - Glass structure KW - Water-bearing glasses KW - High pressure KW - Spectroscopy KW - Glasstruktur KW - Wasserhaltige Gläser KW - Hoher Druck KW - Spektroskopie PY - 2015 DO - https://doi.org/10.1016/j.jnoncrysol.2015.05.004 SN - 0022-3093 VL - 423-424 SP - 58 EP - 67 PB - North-Holland Publ. Co. CY - Amsterdam AN - OPUS4-33804 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bauer, Ute A1 - Behrens, H. A1 - Reinsch, Stefan A1 - Morin, E. I. A1 - Stebbins, J. F. T1 - Structural investigation of hydrous sodium borosilicate glasses N2 - The structural properties of a borosilicate glass with nominal 16 mol% Na2O, 10 mol% B2O3 and 74mol% SiO2 and water contents between 0 and 8wt% H2O (0–22 mol% H2O)were investigated with IR, Raman and 11BMAS NMR spectroscopy. In addition to the pronounced OH stretching vibration band of weakly H-bonded species at 3580 cm−1 the MIR spectra show a triplet at 2900, 2350 and 1750 cm−1, similar as observed in water-bearing silicate glasses. These bands are assigned to OH groups and water molecules which are strongly H-bonded, to non-bridging oxygen. Water species contents determined from absorption bands in the NIR at 5200 cm−1 (molecular H2O), 4700 cm−1 (B\\OH), and 4500 cm−1 (Si\\OH) indicate that hydroxyl groups dominate up to ~6 wt% total H2O. Based on the absorption coefficients known from literature for silicate and borate glasses the B\\OH/Si\\OH ratio is estimated to be ≈0.8. As indicated by density, Raman and NMR data the incorporation ofwater has strong structural impacts in particular at low water contents up to 3 wt% H2O. While the nominally dry glasses still contain a significant fraction (12%) of three-fold coordinated boron, almost all boron is four-fold coordinated in hydrous glasses. The increase of band components in the Raman spectra near 900 cm−1 relative to the region N 1050 cm−1 gives evidence for depolymerization of the network upon hydration. Fitting of the spectra with Gaussians implies that silica tetrahedra with two non-bridging oxygen (Q2) are preferentially formed by reactionwithwater on expense of tetrahedra linked to four tetrahedra (Q4). KW - Glass structure KW - Borosilicate glasses KW - Water-bearing glasses KW - Spectroscopy PY - 2017 DO - https://doi.org/10.1016/j.jnoncrysol.2017.03.023 SN - 0022-3093 SN - 1873-4812 VL - 465 SP - 39 EP - 48 PB - Elsevier B. V. AN - OPUS4-40805 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -