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Characteristics of Dental Restorative Composites Fabricated from Bis-GMA Alternatives and Spiro Orthocarbonates

机译:Bis-GMA替代品和螺正碳酸酯制成的牙科修复复合材料的特性

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摘要

The characteristics of resin matrices containing 2,2-bis[4-(2-hydroxy-3-methacryloyloxy propoxy) phenyl] propane (Bis-GMA) alternatives and spiro orthocarbonate (SOC) were examined to produce dental restorative composites exhibiting lower curing shrinkage and better mechanical strength than the commercially available dental composites. Bis-GMA alternatives were prepared by replacing the hydroxyl groups in Bis-GMA with alkoxy groups. Various SOCs that showed the expected volume expansion during the curing reaction caused by the ring opening reaction were added to Bis-GMA alternatives for a further decrease in curing shrinkage. The curing shrinkage of the dental composites containing Bis-GMA alternative and SOC was always lower than that of the dental composite used as the control, which contained 70 wt% Bis-GMA and 30 wt% triethylene glycol dimethacrylate (TEGDMA) as the resin matrix. Furthermore, the mechanical strength of the dental composites prepared from the 2,2-bis[4-(2-methoxy-3-methacryloyloxy propoxy)phenyl]propane (Bis-M-GMA) mixture containing approximately 10 wt% SOC was higher than that of the dental composite used as the control.
机译:研究了包含2,2-双[4-(2-羟基-3-甲基丙烯酰氧基丙氧基丙氧基)苯基]丙烷(Bis-GMA)替代品和螺碳酸盐(SOC)的树脂基体的特性,以制备固化收缩率较低的牙齿修复复合材料以及比市售牙科复合材料更好的机械强度。通过用烷氧基取代Bis-GMA中的羟基来制备Bis-GMA替代品。 Bis-GMA替代品中添加了各种SOC,这些SOC在开环反应引起的固化反应过程中显示出预期的体积膨胀,可进一步降低固化收缩率。包含Bis-GMA替代品和SOC的牙科复合材料的固化收缩率始终低于用作对照的牙科复合材料的固化收缩率,后者包含70 wt%的Bis-GMA和30 wt%的三乙二醇二甲基丙烯酸酯(TEGDMA)作为树脂基质。此外,由包含约10重量%SOC的2,2-双[4-(2-甲氧基-3-甲基丙烯酰氧基丙氧基)苯基]丙烷(Bis-M-GMA)混合物制备的牙科复合材料的机械强度高于用作对照的牙科复合材料。

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