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Eingeladener Vortrag
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Borosilicate glass has a wide range of technical applications due to its high chemical durability and thermal-shock resistivity. Here the effect of H2O on 16 Na2O, 10 B2O3,74 SiO2 glass is studied over a wide range of water contents from 0 to 8 wt.%. MIR spectra give evidence for the coexistence of strongly and weakly H-bonded hydrous species. Evaluation of NIR bands at 5200 cm-1 (molecular H2O), 4700 cm-1 (B-OH), and 4500 cm-1 (Si-OH) reveal that OH groups dominate up to ~6 wt.% H2O, with B-OH/Si-OH of ≈ 0.8. The incorporation of low amounts of H2O has strong impact on structure. NMR spectra of nominally dry glasses indicate a significant fraction (12 %) of 3-coordinated boron, but almost all boron is 4-coordinated after addition of 3 wt.% H2O. Raman spectra show that hydration results preferentially in transformation of Q4 to Q2 while Q3 remain unchanged, probably stabilized by bonding to BO4 tetrahedra. Viscosity measurements and differential thermal analysis give consistent results, confirming strong decrease of the glass transition temperature with addition of water from 849 K (dry) to 540 K (5 wt% H2O). An additional relaxation mechanism in hydrous glasses is inferred from dynamic mechanical analysis and is assigned to cooperative processes involving hydrous species. It is postulated that this relaxation mechanism plays an important role in crack growth kinetics.
Borosilicate glass has a wide range of technical applications due to its high chemical durability and thermal-shock resistivity. Here the effect of H2O on 16 Na2O, 10 B2O3,74 SiO2 glass is studied over a wide range of water contents from 0 to 8 wt.%. MIR spectra give evidence for the coexistence of strongly and weakly H-bonded hydrous species. Evaluation of NIR bands at 5200 cm-1 (molecular H2O), 4700 cm-1 (B-OH), and 4500 cm-1 (Si-OH) reveal that OH groups dominate up to ~6 wt.% H2O, with B-OH/Si-OH of ≈ 0.8. The incorporation of low amounts of H2O has strong impact on structure. NMR spectra of nominally dry glasses indicate a significant fraction (12 %) of 3-coordinated boron, but almost all boron is 4-coordinated after addition of 3 wt.% H2O. Raman spectra show that hydration results preferentially in transformation of Q4 to Q2 while Q3 remain unchanged, probably stabilized by bonding to BO4 tetrahedra. Viscosity measurements and differential thermal analysis give consistent results, confirming strong decrease of the glass transition temperature with addition of water from 849 K (dry) to 540 K (5 wt% H2O). An additional relaxation mechanism in hydrous glasses is inferred from dynamic mechanical analysis and is assigned to cooperative processes involving hydrous species. It is postulated that this relaxation mechanism plays an important role in crack growth kinetics.
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).