TY - JOUR A1 - Nawaz, Q. A1 - Blaeß, Carsten A1 - Mueller, Ralf A1 - Boccaccini, A.R. T1 - Processing and cytocompatibility of Cu-doped and undoped fluoride-containing bioactive glasses N2 - Sintered or additive-manufactured bioactive glass (BG) scaffolds are highly interesting for bone replacement applications. However, crystallization often limits the high-temperature processability of bioactive glasses (BGs). Thus, the BG composition must combine high bioactivity and processability. In this study, three BGs with nominal molar (%) compositions 54.6SiO2-1.7P2O3-22.1CaO-6.0Na2O-7.9K2O-7.7MgO (13–93), 44.8SiO2-2.5P2O3-36.5CaO-6.6Na2O-6.6K2O-3.0CaF2 (F3) and 44.8SiO2-2.5P2O3-35.5CaO-6.6Na2O-6.6K2O-3.0CaF2-1.0CuO (F3–Cu) were investigated. The dissolution and ion release kinetics were investigated on milled glass powder and crystallized particles (500–600 μm). All glasses showed the precipitation of hydroxyapatite (HAp) crystals after 7 days of immersion in simulated body fluid. No significant differences in ion release from glass and crystalline samples were detected. The influence of surface roughness on cytocompatibility and growth of preosteoblast cells (MC3T3-E1) was investigated on sintered and polished BG pellets. Results showed that sintered BG pellets were cytocompatible, and cells were seen to be well attached and spread on the surface after 5 days of incubation. The results showed an inverse relation of cell viability with the surface roughness of pellets, and cells were seen to attach and spread along the direction of scratches. KW - Bioactive glass KW - Crystallization KW - Solubility KW - Cytocompatibility KW - Surface roughness PY - 2024 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:b43-598257 SN - 2666-5395 VL - 18 SP - 1 EP - 8 PB - Elsevier Ltd. AN - OPUS4-59825 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Drexler, A.-K. A1 - Konert, Florian A1 - Nietzke, Jonathan A1 - Hodžić, E. A1 - Pastore, S. A1 - Domitner, J. A1 - Rhode, Michael A1 - Sommitsch, C. A1 - Böllinghaus, Thomas T1 - Effect of Tensile Loading and Temperature on the Hydrogen Solubility of Steels at High Gas Pressure N2 - The hydrogen solubility in ferritic and martensitic steels is affected by hydrostatic stress, pressure, and temperature. In general, compressive stresses decrease but tensile stresses increase the hydrogen solubility. This important aspect must be considered when qualifying materials for high‐pressure hydrogen applications (e.g., for pipelines or tanks) by using autoclave systems. In this work, a pressure equivalent for compensating the effect of compressive stresses on the hydrogen solubility inside of closed autoclaves is proposed to achieve solubilities that are equivalent to those in pipelines and tanks subjected to tensile stresses. Moreover, it is shown that the temperature effect becomes critical at low temperatures (e.g., under cryogenic conditions for storing liquid hydrogen). Trapping of hydrogen in the microstructure can increase the hydrogen solubility with decreasing temperature, having a solubility minimum at about room temperature. To demonstrate this effect, the generalized law of the hydrogen solubility is parameterized for different steels using measured contents of gaseous hydrogen. The constant parameter sets are verified and critically discussed with respect to the high‐pressure hydrogen experiments. KW - Hydrogen KW - Solubility KW - Temperature KW - Tensile loading KW - Analytical calculation PY - 2023 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:b43-586701 SN - 1611-3683 SP - 1 EP - 9 PB - Wiley AN - OPUS4-58670 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - THES A1 - Usmani, Shirin T1 - Wood treated with nano metal fluorides - relations between composition, size, and durability N2 - In this study, nanoscopic particles of magnesium Fluoride (MgF2) and calcium fluoride (CaF2) also known as nano metal fluorides (NMFs), were evaluated for their potential to improve wood durability. Even though these fluorides are sparingly soluble, their synthesis in the form of nano-sized particles turns them into promising candidates for wood preservation. Their distinct property of low-water solubility is proposed to maintain long-lasting protection of treated wood by reducing the leaching of fluoride. Analytical methods were used to characterize the synthesized NMFs and their distribution in treated wood specimens. Transmission electron microscopy images showed that these fluoride particles are smaller than 10 nm. In nano metal fluoride (NMF) treated specimens, aggregates of these particles are uniformly distributed in the wood matrix as confirmed with scanning electron microscopy images and their corresponding energy-dispersive X-ray spectroscopy maps. The fluoride aggregates form a protective layer around the tracheid walls and block the bordered pits, thus reducing the possible flow path for water absorption into wood. This is reflected in the reduced swelling and increased hydrophobicity of wood treated with NMFs. The biocidal efficacy of NMFs was tested against brown-rot fungi (Coniophora puteanaand Rhodonia placenta), white-rot fungus (Trametes versicolor), and termites (Coptotermes formosanus). The fungal and termite tests were performed in accordance with the EN 113 (1996) and EN 117 (2012) standards, respectively. Prior to fungal tests, the NMF treated wood specimens were leached according to the EN 84 (1997)standard. Compared to untreated specimens, the NMF treated wood specimens have a higher resistance to decay caused by brown-rot fungi, white-rot fungus, and termites. Although all NMF treatments in wood reduce the mass loss caused by fungal decay, only the combined treatment of MgF2 and CaF2 has efficacy against both brown-rot fungi and white-rot fungus. Similarly, wood treated with the combined NMF formulation is the least susceptible to attack by C. formosanus.It is proposed that combining MgF2 and CaF2changes their overall solubility to promote the release of fluoride ions at the optimal concentration needed for biocidal efficacy against fungi and termites. In this thesis, it was proven that even after leaching, sufficient fluoride was present to protect NMF treated wood from fungal decay. This shows that NMFs are robust enough for above ground contact outdoor applications of wood, where permanent wetness cannot be avoided according to Use Class 3.2, as per the EN 335 (2013) standard. Also, they pose a low risk to human health and the environment because they are sparingly soluble. Since NMFs significantly reduce the decay of wood, the CO2 fixed in it will be retained for longer than in unpreserved wood. Overall, the novel results of this study show the potential of NMFs to increase the service life of building materials made from non-durable wood. KW - Termites KW - Nano metal fluorides KW - Solubility KW - Wood protection KW - Fungi PY - 2021 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:b43-525108 SP - i EP - 118 PB - Humboldt-Universität zu Berlin CY - Berlin AN - OPUS4-52510 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Simões, R. G. A1 - Melo, P. L. T. A1 - Bernardes, C. E. S. A1 - Heilmann, Maria A1 - Emmerling, Franziska A1 - Minas da Piedade, M. E. T1 - Linking Aggregation in Solution, Solvation, and Solubility of Simvastatin: An Experimental and MD Simulation Study N2 - The solubility is generally thought to be higher if the solvent effectively solvates solute molecules that are well-separated from each other. The present work suggests, however, that the formation of large solute aggregates does not necessarily imply less effective solvation and lower solubility. Measurements of the solubility of simvastatin (one of the most commonly prescribed antihyperlipidemic drugs) in three solvents with different polarities and protic characters, led to the solubility order acetone > ethyl acetate > ethanol, in the full temperature range covered by the experiments (283–308 K). An analysis of the structures of the different solutions on the basis of molecular dynamics simulation results indicated that this trend seems to be determined by a balance between the solute tendency toward aggregation and the ability of the solvent to efficiently solvate it, by integrating the cluster structures, regardless of their size, and effectively establishing solvent–solute interactions. KW - Simvastatin KW - Solubility KW - API KW - Aggregation PY - 2021 U6 - https://doi.org/10.1021/acs.cgd.0c01325 VL - 21 IS - 1 SP - 544 EP - 551 AN - OPUS4-52185 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Oesch, Tyler A1 - Weise, Frank A1 - Marx, Heidi A1 - Kositz, M. A1 - Huenger, K.-J. T1 - Analysis of the porosity of alkali-sensitive aggregates for the assessment of microstructure-dependent solubility in the context of ASR N2 - Intensified Alkali-Silica Reaction (ASR) damage has occurred on German roadways in recent years, leading to requirements for compulsory pre-construction investigation of aggregate alkali sensitivity using concrete tests with external alkali supply. However, since these tests are time-consuming and cost-intensive, there is interest in replacing them with a solubility test on pure aggregate in 0.1 M KOH solution at 80°C with a defined NaCl content (1wt.-%). In this context, the influence of aggregate pore structure on SiO2 and Al2O3 solubility was investigated in this project. This paper compares the results of porosity studies with X-ray Computed Tomography (3D-CT) and the Brunauer-Emmett-Teller (BET) method on individual quarried and river gravel granules of both rhyolite and greywacke. For visualization and quantification of both externally accessible and fully enclosed surfaces of granules using X-ray 3D-CT, special software tools were developed. The results demonstrated that the river gravel granules had significantly larger externally accessible surfaces than the quarried granules. BET measurements on individual stones showed, as expected, that measured surfaces were about three orders of magnitude larger than those from the X-ray 3D-CT analyses due to the higher spatial resolution of BET. There was no apparent correlation between the X-ray 3D-CT and BET surface areas. Mercury porosimetry measurements indicate that this may be due to the presence of significant porosity below the spatial resolution of the X-ray 3D-CT. A comparison of SiO2 and Al2O3 solubility measurements with the X-ray 3D-CT and BET surface area data resulted only in weak, inconclusive correlations, indicating the need for further experimental investigation. T2 - Microdurability Webinar CY - Online meeting DA - 12.10.2020 KW - X-ray Computed Tomography (CT) KW - Brunauer-Emmett-Teller (BET) Method KW - Alkali-Silica Reaction (ASR) KW - Porosity KW - Solubility PY - 2020 AN - OPUS4-51429 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 - CONF A1 - Vogel, Christian A1 - Kalbe, Ute A1 - Simon, Franz-Georg T1 - Leaching behavior of Antimony in MSWI bottom ash N2 - Bottom ash (BA) from municipal solid waste incineration (MSWI) contains harmful substances such as heavy metals, chloride and sulfate which are mobilized in contact with water. Standardized leaching tests are used to measure the extent of mobilization. It is known that fresh bottom ash displays elevated concentrations of various heavy metals such as lead or zinc due to the formation of hydroxo complexes as a result of high pH values of 12 and above. Storage of BA is accompanied by ageing processes, mainly the reaction of CaO and Ca(OH)2 with CO2 leading to lower pH values in contact with water around 11. Usually heavy metals concentrations are minimum at these conditions. Knowledge of the long-term leaching behavior of potentially harmful substances is crucial for the assessment of the environmental compatibility of reusing municipal solid-waste incineration bottom ash (MSWI BA) in construction, i.e., as a road base layer. BA fractions obtained from wet-processing aiming at the improvement of environmental quality were used to investigate the mobility of relevant substances. Eluates from laboratory-scaled leaching procedures (column percolation and lysimeters) were analyzed to learn about the long-term release of substances. Unsaturated conditions and artificial rainwater were used in the lysimeter tests to simulate field conditions. In addition, batch test eluates were generated at usual liquid-to-solid ratios (L/S) for compliance testing purposes. A variety of cations and anions was measured in the eluates. The wet treatment reduces the leaching of chloride and particularly sulfate by more than 60%. The release of typical contaminants for the treated MSWI BA such as the heavy metals Cu and Cr was well below 1% in the conducted leaching tests. An increase in the Sb concentration was observed in the lysimeter experiments starting at L/S 0.75 L/kg and in the column experiment at L/S 4 L/kg is assumed to be related to decreasing concentrations of Ca and thus to the dissolution of sparingly soluble calcium antimonate. The same leaching mechanism applies with V, but the concentration levels observed are less critical regarding relevant limit values. However, on the long term the behavior of Sb could be problematic for the application of MSWI BA as secondary building material. T2 - MINEA Final Conference CY - Bologna, Italy DA - 20.02.2020 KW - Antimony KW - Bottom ash KW - Leaching KW - Solubility PY - 2020 AN - OPUS4-50450 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bhattacharya, Biswajit A1 - Das, S. A1 - Lal, G. A1 - Soni, S. R. A1 - Ghosh, A. A1 - Reddy, C. M. A1 - Ghosh, S. T1 - Screening, crystal structures and solubility studies of a series of multidrug salt hydrates and cocrystals of fenamic acids with trimethoprim and sulfamethazine N2 - Multidrug solids have a potential use to efficiently treat and control a superfluity of medical conditions. To address the current drawbacks of drug development in R&D, it was targeted to achieve new pharmaceutical solid forms of fenamic acids having improved solubility and thermal stability. Subsequently, five new multicomponent solids consisting of three salt hydrates of trimethoprim (TMP) with mefenamic acid (TMP-MFA-H2O), tolfenamic acid (TMP-TFA-H2O) and flufenamic acid (TMP-FFA-H2O), and two cocrystals of sulfamethazine (SFZ) with flufenamic acid (SFZ-FFA) and niflumic acid (SFZ-NFA) were prepared by liquid assisted grinding. Looking at the structures of active pharmaceutical ingredient (API) molecules, it was quite expected that a wide range of supramolecular synthons would lead to cocrystallization. New forms were characterized thoroughly by various solid-state techniques, including single crystal X-ray diffraction (SCXRD), which provided details of hydrogen bonding, molecular packing and interactions between drug and coformer. Kinetic solubility at pH 7.4 buffer study has been carried out and a comparison is made with respect to the parent drugs. A significant enhancement of NSAIDs solubility was observed in all salt hydrate systems of TMP. Thus with increasing physicochemical properties such as improved solubility further leads to the enhancement of bioavailability, which has implications to overcoming the formulation related problems of active pharmaceutical ingredients (APIs). KW - Cocrystals KW - Crystal engineering KW - Solubility PY - 2020 U6 - https://doi.org/10.1016/j.molstruc.2019.127028 SN - 0022-2860 VL - 1199 SP - 127028 PB - Elsevier B.V. AN - OPUS4-49873 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Müller, Ralf A1 - Körner, S. T1 - Dissolution and reprecipitation of silver in sintering silver-glass dispersions N2 - Electric contacts based on silver-glass dispersions are key components in optoelectronic microsystems and control modules for medical, information & communication and energy technology in our networked society. Driven by the complexity of modern production processes and ever shorter time-to-market requirements, the fast and specific development of tailored silver-glass dispersions has become a bottleneck of technology development. Nevertheless, the underlying mechanisms of silver dissolution, transport, and reprecipitation, and the resulting micro structure evolution during firing are poorly understood. The broad literature on the precipitation of colloidal silver particles and the related processes of silver dissolution and diffusion mostly refer to very small volume fractions of silver. Transferring these results to the sintering of glass-containing silver dispersions, is therefore highly questionable. In this case, silver dissolution, electrical contact between silver particles, transport and reprecipitation take place under special conditions. This includes short diffusion lengths (particle size < 10 μm), the presence of three-phase contacts silver - glass - sintering atmosphere, as well as silver reprecipitation at the sintering contacts as the driving force of silver transport. Here, a dynamic balance of the silver concentration can be expected to result from the ratio between silver dissolution and reprecipitation. The aim of the project is to gain basic insight into the mechanisms of dissolution, transport and reprecipitation of silver in sintering silver glass dispersions. In this context, the main focus is on gaining basic knowledge about the dissolution of metallic silver in low melting oxide glasses as the limiting factor of the sintering of silver-glass composites. In particular, we will strive to gain insight into the effect of the oxygen content of the sintering atmosphere, of the oxygen dissolved in the silver particles, of silver oxide on the surface of the silver powder, of the electric contact between the silver particles, as well as the basicity of the glass. Furthermore, we strive for insights into the silver mobility and the silver concentration that can be attained (silver solubility) in oxide glasses with a low melting point. Summing up all these aspects, a closed explanatory model for silver dissolution, transport and reprecipitation during the sintering of glass silver dispersions will be introduced. T2 - DFG Begutachtungskolloquium (PAK 949/1 und PAK 950/1) CY - Bonn, Germany DA - 07.03.2017 KW - Sintering KW - Silver KW - Glass KW - Solubility KW - Reprecipitation PY - 2017 AN - OPUS4-44228 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Müller, Ralf A1 - Körner, S. T1 - Dissolution and reprecipitation of silver in sintering silver-glass dispersions N2 - Electric contacts based on silver-glass dispersions are key components in optoelectronic microsystems and control modules for medical, information & communication and energy technology in our networked society. Driven by the complexity of modern production processes and ever shorter time-to-market requirements, the fast and specific development of tailored silver-glass dispersions has become a bottleneck of technology development. Nevertheless, the underlying mechanisms of silver dissolution, transport, and reprecipitation, and the resulting micro structure evolution during firing are poorly understood. The broad literature on the precipitation of colloidal silver particles and the related processes of silver dissolution and diffusion mostly refer to very small volume fractions of silver. Transferring these results to the sintering of glass-containing silver dispersions, is therefore highly questionable. In this case, silver dissolution, electrical contact between silver particles, transport and reprecipitation take place under special conditions. This includes short diffusion lengths (particle size < 10 μm), the presence of three-phase contacts silver - glass - sintering atmosphere, as well as silver reprecipitation at the sintering contacts as the driving force of silver transport. Here, a dynamic balance of the silver concentration can be expected to result from the ratio between silver dissolution and reprecipitation. The aim of the project is to gain basic insight into the mechanisms of dissolution, transport and reprecipitation of silver in sintering silver glass dispersions. In this context, the main focus is on gaining basic knowledge about the dissolution of metallic silver in low melting oxide glasses as the limiting factor of the sintering of silver-glass composites. In particular, we will strive to gain insight into the effect of the oxygen content of the sintering atmosphere, of the oxygen dissolved in the silver particles, of silver oxide on the surface of the silver powder, of the electric contact between the silver particles, as well as the basicity of the glass. Furthermore, we strive for insights into the silver mobility and the silver concentration that can be attained (silver solubility) in oxide glasses with a low melting point. Summing up all these aspects, a closed explanatory model for silver dissolution, transport and reprecipitation during the sintering of glass silver dispersions will be introduced. T2 - DFG Begutachtungskolloquium (PAK 949/1 und PAK 950/1) CY - Bonn, Germany DA - 07.03.2017 KW - Sintering KW - Silver KW - Glass KW - Solubility KW - Reprecipitation PY - 2017 AN - OPUS4-44227 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Woydt, Mathias A1 - Mohrbacher, H. T1 - The tribological property profile of hard metals and metal matrix composites based on niobium carbide N2 - This work is focused on the tribological profile of NbC-based material, as well as their potential applications and environmental implications. T2 - International Symposium on Wear Resistant Alloys for the Mining and Processing Industry CY - Sao Paulo, Brazil DA - 04.05.2015 KW - Niobium carbide KW - Metal KW - Binder KW - Metal matrix composite KW - Friction KW - Wear KW - Hardness KW - Solubility KW - Toughness KW - Abrasion PY - 2018 SN - 978-0-692-05382-9 SP - 427 EP - 461 AN - OPUS4-44201 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kronemann, Jens T1 - Zur zeitlichen Abhängigkeit von Löseprozessen in hochalkalischen Lösungen zur Charakterisierung der Alkaliempfindlichkeit von Gesteinskörnungen N2 - Die schädigende Alkali-Kieselsäure-Reaktion (AKR) im Beton stellt in Teilbereichen nach wie vor ein Problem bei der Bewertung der Dauerhaftigkeit von Beton dar. Eine der häufigsten Fragestellungen ist immer noch eine schnelle und sichere Beurteilung der Alkaliempfindlichkeit von Gesteinskörnungen für die Betonherstellung. In der Präsentation wird gezeigt, welchen Beitrag die Gesteinskörnung zur AKR im Beton hat. Dabei wird die Alkaliempfindlichkeit von Gesteinskörnungen quantifiziert und die zu erwartende Schädigung des Betons durch die Gesteinskörnung detaillierter als bisher möglich klassifiziert. Im Vordergrund der Präsentation steht dabei das Verständnis der Auflösungsprozesse von Gesteinskörnungen in KOH-Lösungen (pH ≥ 13) bei unterschiedlichen Reaktionsbedingungen. Anhand von Löseversuchen an den originalen Lieferkörnungen der Gesteinskörnungen bei 40 °C und mit 1,0 M KOH-Lösung ist es möglich, die Reaktivität der Gesteinskörnungen mit den ermittelten SiO2- und Al2O3-Konzentrationen der alkalischen Lösungen zu beschreiben. Durch eine erhöhte Temperatur von 80 °C und eine abgesenkte Konzentration der KOH-Lösung von 0,1 M können innerhalb von 56 Tagen vergleichbare Ergebnisse zu den Resultaten der Löseversuche bei 40 °C und 1,0 M KOH-Lösung erreicht werden. In der alkalischen Lösung wird ein bestimmter Teil des gelösten SiO2 durch ebenfalls vorhandenes Al2O3 alumosilikatisch gebunden. Der verbleibende Teil des gelösten SiO2 steht für eine AKR zur Verfügung. Aus der zeitabhängigen Darstellung dieser SiO2-Konzentration wird die Lösegeschwindigkeit ermittelt. Dabei werden vier aufeinanderfolgende Phasen dem Dehnungs- und Rissbreitenverlauf der Probekörper des 40 °C-Betonversuchs zugeordnet. Zur Beurteilung der Alkaliempfindlichkeit einer Gesteinskörnung sind die Lösegeschwindigkeiten der letzten drei Phasen entscheidend. Die Methode bietet eine Möglichkeit, die Alkaliempfindlichkeit einer Gesteinskörnung schnell, sicher und genauer als bisher zu bestimmen. Besonders vorteilhaft sind dabei die direkte Prüfung der Gesteinskörnung an der originalen Korngröße (Lieferkörnung), die zementunabhängige Prüfung, sowie die einfache experimentelle Durchführung und Auswertung. T2 - 15. Baustoffkolloquium CY - Cottbus, Germany DA - 08.03.2016 KW - Alkali-Kieselsäure-Reaktion KW - Alkaliempfindlichkeit KW - Gesteinskörnung KW - Lösegeschwindigkeit KW - Löslichkeit KW - Aggregate KW - Alkali reactivity KW - Alkali-silica reaction KW - Dissolution rate KW - Solubility PY - 2016 AN - OPUS4-35607 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ried, Peter A1 - Gaber, Martin A1 - Müller, Ralf A1 - Deubener, J. T1 - Hydrogen permeability of a barium-aluminoborosilicate glass - A methodical approach N2 - The H2 effusion from H2 saturated glass powders, H2 permeation through the wall of blown glass bulbs, and H2 permeation through the wall of glass capillaries were applied to evaluate the permeability of hydrogen gas in a barium-aluminoborosilicate (BABS) glass. To validate these methods, two commercial glasses (vitreous silica and borosilicate) were used as a reference. Permeation values obtained from the different experiments agreed within a factor of 3 or less. The H2 permeability of BABS glass at temperatures close to ambient was found to be at least 3 orders of magnitude below that of borosilicate and silica glasses. The powder method, which requires minimal sample preparation efforts, turned out to provide easy access to the measurement of H2 permeability of glasses down to P = 3.9 × 10- 21 mol s- 1 Pa- 1 m- 1. KW - Hydrogen gas KW - Permeability KW - Solubility KW - Diffusivity KW - Aluminoborosilicate glass PY - 2014 U6 - https://doi.org/10.1016/j.jnoncrysol.2014.04.006 SN - 0022-3093 VL - 394-395 SP - 43 EP - 49 PB - North-Holland Publ. Co. CY - Amsterdam AN - OPUS4-30720 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dressler, M. A1 - Börnstein, Julian A1 - Meinel, M. A1 - Ploska, Ute A1 - Reinsch, Stefan A1 - Hodoroaba, Vasile-Dan A1 - Nicolaides, Dagmar A1 - Wenzel, Klaus-Jürgen T1 - Sol-gel preparation of calcium titanium phosphate: viscosity, thermal properties and solubility N2 - Calcium titanium phosphate (CTP) was prepared by the sol–gel route in order to prepare suitable coatings. This work addresses the question of how to prepare stable CTP sols. Their rheological properties as a function of process parameters like solid loading and water content are investigated. It was found that an increased solid loading as well as an increased water content lead to an increased initial viscosity as well as a more pronounced ageing induced viscosity rise. In addition, the thermal behavior of the resulting xerogels was analyzed. Furthermore, we studied the ion release behavior of the xerogels when brought in contact with water. Results suggest that calcium titanium phosphate shows a diffusion controlled ion release mode with a preferential release of Ca. KW - Calcium titanium phosphate KW - Sol-gel processing KW - Rheology KW - Thermal analysis KW - Coatings KW - Solubility PY - 2012 U6 - https://doi.org/10.1007/s10971-011-2653-y SN - 0928-0707 SN - 1573-4846 VL - 62 IS - 3 SP - 273 EP - 280 PB - Kluwer Academic Publ. CY - Dordrecht AN - OPUS4-27617 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dombrowski, Felix A1 - Marx, Heidi A1 - Ploska, Ute A1 - Nicolaides, Dagmar A1 - Stiller, M. A1 - Knabe, C. A1 - Berger, Georg T1 - Solubility and ingrowth behaviour of degradable and figuline calcium alkaline phosphate cements N2 - The thrust of the investigations presented here is to point out the degradation behaviour in vitro and the ingrowth behaviour in vivo of four different calcium alkaline phosphate cements. Two of the figuline and mouldable composites consist of the crystalline phase Ca2KNa(PO4)2 and two of the crystalline phase Ca10[K/Na](PO4)2 each containing 2wt% medium gel strength porcine gelatin. Furthermore A-TCP was added to both Ca10[K/Na](PO4)2 cements as a hardening supporting reactant. The testing material groups differ in small amorphous portions containing either silica phosphate (GB9), magnesium potassium phosphate (GB14) or diphosphates (401545 and 401545(70)). The respective composites show a monomodal particle size distribution (d50~7µm; span~4) and an average total porosity around 28vol%.For the solubility studies cylindrical samples (d=6mm; h=12mm) were stored in a 0.1mol TRIS buffer solution and incubated at 37°C for maximum 50 weeks. The storage solution was analysed and renewed every week. The results are plotted cumulative. For the in vivo studies critical size defects were dissected to mandibles in a sheep model in which a 1cm³ area of the bottom of the mandibles was surgically resected and replaced with the figuline cements whereas the mouldability allows the reconstruction of the original outer contour without draining off even when replacing upside down. KW - Calcium alkaline phosphate cement KW - Gelatin KW - Figuline KW - Solubility KW - Ingrowth behavior PY - 2012 U6 - https://doi.org/10.4028/www.scientific.net/KEM.493-494.387 SN - 1013-9826 VL - 493-494 SP - 387 EP - 390 PB - Trans Tech Publ. CY - Aedermannsdorf AN - OPUS4-24924 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dabah, Eitan A1 - Kannengießer, Thomas A1 - Eliezer, D. A1 - Böllinghaus, Thomas T1 - In situ analysis of hydrogen behaviour in stainless steels by high energy synchrotron radiation N2 - Hydrogen generally causes lattice distortions and phase transformations when introduced into a metal matrix. The present contribution provides a report of first in situ investigations of hydrogen effects on the lattice of the austenite and the martensite phase in a supermartensitic stainless steel using hard synchrotron radiation for respective energy dispersion diffraction measurements. Lattice distortions, such as the planar spacing expansion, have been monitored during the complete hydrogen effusion process over 24 h and are directly correlated to the dissolved hydrogen in the metal matrix. Among other results, it turned out that hydrogen at the introduced concentration level causes a reversible lattice expansion and after hydrogen effusion the lattice nearly regained its original dimensions. Hydrogen much more significantly affects the austenite phase with respect to lattice expansion than the martensite phase, but no phase transformations occur during the hydrogen desorption process. KW - Hydrogen diffusion KW - Solubility KW - Lattice distortions KW - Energy dispersive X-ray diffraction PY - 2011 U6 - https://doi.org/10.1016/j.msea.2010.10.090 SN - 0921-5093 SN - 1873-4936 VL - 528 IS - 3 SP - 1608 EP - 1614 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-22849 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lim, B.-H. A1 - Choe, W.-H. A1 - Shim, J.-J. A1 - Ra, C. S. A1 - Tuma, Dirk A1 - Lee, H. A1 - Lee, C. S. T1 - High-pressure solubility of carbon dioxide in imidazolium-based ionic liquids with anions [PF6] and [BF4] N2 - The solubility of carbon dioxide in three ionic liquids (ILs) under supercritical fluid condition was measured at pressures up to 32 MPa and at temperatures of 313.15, 323.15, and 333.15 K in a high-pressure view cell. The imidazolium-derivative ionic liquids 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF6]), 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF4]), and 1-octyl-3-methylimidazolium tetrafluoroborate ([omim][BF4]) were employed in this research. The effects of pressure, temperature, nature of anion and cation as well as the water content on the solubility of CO2 in the ILs were investigated experimentally. The solubility of CO2 in the IL was higher for the ILs with longer cationic alkyl group and for the ILs with lower anion polarity. The lower the water content or the lower the temperature as well as the higher the pressure, the higher was the solubility of CO2. KW - Solubility KW - Carbon dioxide KW - Ionic liquid KW - Water content KW - Anion KW - Cation KW - Ionische Flüssigkeiten KW - Gaslöslichkeiten PY - 2009 SN - 0256-1115 VL - 26 IS - 4 SP - 1130 EP - 1136 PB - Inst. CY - Seoul AN - OPUS4-19579 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gildenhaar, Renate A1 - Berger, Georg A1 - Lehmann, Erhard A1 - Stiller, M. A1 - Koch, C. A1 - Ducheyne, P. A1 - Rack, A. A1 - Seligmann, H. A1 - Jonscher, S. A1 - Knabe, C. T1 - A comparative study of the biodegradability of calcium-alkali-orthophosphate ceramics in vitro and in vivo KW - Calcium-alkali-orthophosphate KW - Solubility KW - Biodegradability PY - 2007 SN - 1013-9826 VL - 330-332 SP - 63 EP - 66 PB - Trans Tech Publ. CY - Aedermannsdorf AN - OPUS4-14528 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Berger, Georg A1 - Ploska, Ute A1 - Willmann, G. T1 - Hydroxyapatite's Solubility May Cause Loosening of Coated Implants KW - pH Value KW - Solubility KW - Coated Implants KW - Hydroxyapatite PY - 2001 SN - 1013-9826 VL - 192-195 SP - 111 EP - 114 PB - Trans Tech Publ. CY - Aedermannsdorf AN - OPUS4-1045 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -