The aim of this study was to compare, in different periods of time, the compressive and diametral tensile strength of a traditional high viscous glass ionomer cement: Fuji IX (GC Corporation), with two new Brazilian GIC's: Vitro-Molar (DFL) and Bioglass R (Biodinamica), all indicated for the Atraumatic Restorative Treatment (ART) technique. Fifteen disk specimens (6.0mm diameter x 3.0mm height) for the diametral tensile strength (DTS) test and fifteen cylindrical specimens (6.0mm diameter x 12.0mm height) for the compressive strength (CS) test were made of each GIC. Specimens were stored in deionized water at 37º C and 100% of humidity in a stove until testing. Five specimens of each GIC were submitted to CS and DTS test in each period, namely 1 hour, 24 hours and 7 days. The specimens were tested in a testing machine (Emic) at a crosshead speed of 1.0mm/min for CS and 0.5mm/min for the DTS test until failure occurred. The data were submitted to two-way ANOVA and Tukey tests (alpha=0.05). The mean CS values ranged from 42.03 to 155.47MPa and means DTS from 5.54 to 13.72 MPa, with test periods from 1h to 7 days. The CS and DTS tests showed no statistically significant difference between Fuji IX and Vitro Molar, except for CS test at 1-hour period. Bioglass R had lowest mean value for CS of the cements tested. In DTS test Bioglass R presented no statistically significant differences when compared with all others tested GICs at 1-hour period and Bioglass R presented no difference at 24-hour and 7-day periods when compared to Vitro-Molar. Further studies to investigate other physical properties such as fracture toughness and wear resistance, as well as chemical composition and biocompatibility, are now needed to better understand the properties of these new Brazilian GIC's.
Experimental dental resins composed of triethyleneglycol dimethacrylate, urethane dimethacrylate, ethoxylated bisphenol-A-dimethacrylate and bisphenol A glycidyl methacrylate containing an organoclay as filler were prepared by photopolymerization. The addition of organoclay fillers results in slower polymerization rates (0.59 and 0.24 mol L -1 min -1 , for the formulations without and with 15% of organoclay, respectively) and lower degrees of conversion (0.50 and 0.35 for the formulations without and with 15% of organoclay), as determined by photocalorimetry. The influence of the organoclay on the thermal and mechanical properties of the resins was evaluated using thermogravimetric analysis (TGA) and dynamic mechanical analysis (DMA) techniques. The (tan δ) and E´ curves indicate the formation of more rigid materials and the damping curve data indicates more homogeneous materials. An increase of storage modulus, E', was observed for composites with the higher organoclay filler contents. These effects are due to the higher viscosity of the systems with organoclay, resulting in a lower mobility of the radicals during the propagation step of polymerization, as well as to the scattering of the incident photopolymerizing radiation, which lowers the amount of initiation centres.
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