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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.
Surface water-induced broadening of crack initiation probability of zinc aluminosilicate glasses
(2017)
The crack generation probability by Vickers indentation of glass surfaces is known to be influenced by the atmospheric conditions under which the Vickers experiment is performed [1]. However, the effect of surface water due to preparation and storage of the glass surfaces prior to the indentation is less understood. Therefore, zinc aluminosilicate glasses of perzinc, peraluminous as well as nominally NBO-free meta-aluminous composition were prepared by melt quenching. Surfaces of cut and polished specimens of these glasses were either stored for seven days under constant atmosphere (50 °C; 55% RH) or etched (HF: 20vol%; 20 min) shortly before indentation. The obtained results show a strong variation of crack initiation behavior depending on chemical composition of the glasses as well as sample preparation. All experiments were performed in dry nitrogen gas to minimize the influence of atmospheric humidity during indentation. While the regular glass surfaces exposed to humid air prior to Vickers indentation show a broad distribution of crack initiation probability, this distribution narrows down if etched glass surfaces are tested. SNMS depth profiling shows a water enriched layer at the surface (150 μm) for the non-etched and stored specimens leading to the conclusion that surface water causes broadening of the crack initiation probability of glass surfaces.
Bulk elastic properties, hardness and fatigue of calcium aluminosilicate (CAS) glasses in the technically relevant region of the ternary with intermediate-silica fraction were determined by combining results of Vickers indentation, ultrasonic echography and Archimedian buoyancy at room temperature. Of three studied compositional series, the first series was along the meta-aluminous join, while in the two other series the molar fraction of SiO2 was kept constant. For the first series the elastic moduli and hardness show an almost linear increase with increasing SiO2 fraction. In contrast, increasing the CaO/SiO2 ratio at constant silica content results in a characteristic change when passing the meta-aluminous join. Elastic constants and hardness were lower at the percalcic than on the peraluminous side. Empirical models which relate bulk elastic moduli to internal energy, short-range inter-atomic forces and the packing density of their oxide constituents were found to be in agreement with the experimental data for meta-aluminous glasses, while deviations between the observed and predicted trends were evident for percalcic compositions. Empirical fatigue parameters such as the probability to initiate cracks after indentation reflect the bulk mechanical properties in the CAS system when conducted in inert atmosphere, but are otherwise clearly dominated by environmental effects