Compositional Effects on Indentation Mechanical Properties of Chemically Strengthened TiO2-Doped Soda Lime Silicate Glasses

TiO2 is an important oxide for property modifications in the conventional soda lime silicate glass family. It offers interesting optical and mechanical properties, for instance, by substituting heavy metals such as lead in consumer glasses. The compositional effects on the hardness, reduced elastic modulus and crack resistance as determined by indentation of chemically strengthened (CS) TiO2-doped soda lime silicate glass was studied in the current paper. The CS, which was performed by a K+ for Na+ ion exchange in a molten KNO3 salt bath at 450 °C for 15 h, yielded significant changes in the indentation mechanical properties. The hardness of the glass samples increased, and this was notably dependent on the SiO2, CaO and TiO2 content. The reduced elastic modulus was less affected by the CS but showed decrease for most samples. The crack resistance, an important property in many applications where glasses are subjected to contact damage, showed very different behaviors among the series. Only one of the series did significantly improve the crack resistance where low CaO content, high TiO2 content, high molar volume and increased elastic deformation favored an increased crack resistance.

Visualization of Spatial Charge in Thermally Poled Glasses via Nanoparticles Formation

It is shown for the first time that the vacuum poling of soda-lime silicate glass and the subsequent processing of the glass in a melt containing silver ions results in the formation of silver nanoparticles buried in the subanodic region of the glass at a depth of 800–1700 nm. We associate the formation of nanoparticles with the transfer of electrons from negatively charged non-bridging oxygen atoms to silver ions, their reduction as well as their clustering. The nanoparticles do not form in the ion-depleted area just beneath the glass surface, which indicates the absence of a spatial charge (negatively charged oxygen atoms) in this region of the vacuum-poled glass. In consequence, the neutralization of the glass via switching of non-bridging oxygen bonds to bridging ones, which leads to the release of oxygen, should occur in parallel with the shift of calcium, magnesium, and sodium ions into the depth of the glass.

Coupling Raman, Brillouin and Nd3+ Photo Luminescence Spectroscopy to Distinguish the Effect of Uniaxial Stress from Cooling Rate on Soda–Lime Silicate Glass

Evolution of spectroscopic properties of a soda–lime silicate glass with different thermal history and under applied uniaxial stress was investigated using Raman and Brillouin spectroscopies as well as Nd3+ photoluminescence techniques. Samples of soda–lime silicate with a cooling rate from 6 × 10−4 to 650 K/min were prepared either by controlled cooling from the melt using a differential scanning calorimeter or by a conventional annealing procedure. Uniaxial stress effects in a range from 0 to −1.3 GPa were investigated in situ by compression of the glass cylinders. The spectroscopic observations of rearrangements in the network structure were related to the set cooling rates or the applied uniaxial stress to calculate an interrelated set of calibrations. Comparing the results from Raman and Brillouin spectroscopy with Nd3+ photoluminescence analysis, we find a linear dependence that can be used to identify uniaxial stress and cooling rate in any given combination concurrently. The interrelated calibrations and linear dependence models are established and evaluated, and equations relating the change of glass network due to effects of cooling rate or uniaxial stress are given.