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A V Chadwick

Publications and source records attributed to A V Chadwick.

3 recordsLinked to original sources

Water sorption in resin-modified glass-ionomer cements: an in vitro comparison with other materials.

The pattern of water uptake into a polyacid-modified composite resin (compomer), Dyract (D), was assessed using gravimetric analysis and tritiated water absorption. The results were compared with a resin composite, Herculite (H), a resin-modified glass-ionomer, Fuji II LC (FL), and a conventional glass-ionomer, Fuji II (F). Samples were stored in tritiated water for periods varying between 6 h and 6 months. The resulting change in gravimetric weight and dimensions was recorded. The tritiated water content was then assessed using liquid scintillation counting and this was compared to the gravimetric changes. The inherent water content of each material was also established. D and H showed a slow steady net uptake to 3% and 1.3% weight by volume (WV) respectively at 6 months. FL showed a rapid uptake reaching 8.9% WV at 7 days and 9.3% WV at 6 months. F showed a steady, less dramatic water uptake reaching 5.3% WV by 6 months. For the glass-ionomer materials, values for gravimetric water uptake and tritium release differed due to the ongoing acid base reaction and an increase in firmly bound water. This phenomenon was noted in D suggesting evidence of a similar reaction in this material.

Absorption↗

Examination of the mixed-alkali effect in (Li,Na) disilicate glasses by nuclear magnetic resonance and conductivity measurements.

Results from 29Si, 23Na and 7Li magic-angle spinning nuclear magnetic resonance (NMR) spectroscopy, 7Li NMR relaxation and electrical conductivity in a series of [Li(1-x).Nax]2O.2SiO2 (disilicate) glasses are used to investigate the mixed-alkali effect. From the 29Si NMR spectra there is relatively little change of the network with alkali composition. 23Na and 7Li NMR linewidths and shifts change continuously as a function of composition, indicating that the alkali ions are intimately and uniformly mixed rather than separated into lithium and sodium-rich domains. The activation energy from electrical conductivity shows a distinct maximum at the central composition (x = 0.5), whereas the local activation energy for lithium motion determined from NMR shows only a smaller but monotonic increase as the lithium-content decreases.

Electric Conductivity↗