germanium and zinc-silicate

To elucidate the mechanism(s) responsible for the profound impact germanium has on the setting reaction of zinc silicate glass ionomer cements (GICs).. Five <45μm glass powder compositions (0.48-xSiO2, xGeO2, 0.36 ZnO, 0.16 CaO; where x=0.12, 0.24, 0.36, 0.48mol. fraction) were synthesized. Glass degradation was assessed under simulated setting conditions using acetic acid from 0.5 to 60min, monitoring the concentrations of ions released using ICP-OES. Subsequently, GICs were prepared by mixing fresh glass powders with polyacrylic acid (PAA, Mw=12,500g/mol, 50wt% aq. solution) at a 1:0.75 ratio. Cement structure and properties were evaluated using ATR-FTIR and rheology (for 60min), as well as 24h biaxial flexural strength.. Reduced Si:Ge ratios yielded faster degrading glasses, yet contrary to expectation, the corresponding ATR-FTIR spectra indicated slower crosslinking within the GIC matrix. Rheology testing found the initial viscosity cement pastes reduced with decreased Si:Ge, and Ge containing cements all set significantly slower than the Si based GIC. Interestingly, biaxial flexural strength remained consistent regardless of setting behavior.. This counter-intuitive combination of behaviors is attributed to the presence of a chemical complex species specific to Ge-containing glasses that delays, but does not hinder, the formation of the GIC matrix. These findings embody chemical complex species as a mechanism to decouple glass reactivity from cement setting rate, a mechanism with the potential to enhance the utility of GICs in both dental and orthopaedic applications.

Topics: Calorimetry; Compressive Strength; Dental Restoration Failure; Germanium; Glass Ionomer Cements; Materials Testing; Powders; Silicates; Spectrophotometry, Atomic; Spectroscopy, Fourier Transform Infrared; Viscosity; X-Ray Diffraction; Zinc Compounds