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首页> 外文期刊>Journal of Applied Polymer Science >Effects of water on the long-term properties of Bis-GMA and Silylated-(Bis-GMA) polymers
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Effects of water on the long-term properties of Bis-GMA and Silylated-(Bis-GMA) polymers

机译:水对Bis-GMA和甲硅烷基化(Bis-GMA)聚合物长期性能的影响

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Bis-GMA (2,2-bis-[4-(2-hydroxy-3-methacryloxypropoxy)phenyl]propane) is a viscous hygroscopic monomer which is used with triethyleneglycol-dimethacrylate (TEGDMA) for dental restorations. Bis-GMA was silylated with dimethyl-isopropyl-siloxane and further polymerized in order to increase water resistance and viscosity. The viscosity of the silylated monomer, Sil center dot Bis-GMA, was 50 times lower than that of the parent monomer. After 1 month in water, poly(Bis-GMA/TEGDMA) absorbed 2.6% water and the silylated polymer, poly(Sil center dot Bis-GMA), only 0.56%. During this process water extracted residual monomer from each polymer. The behavior of water sorption and desorption as a function of time in poly(Sil center dot Bis-GMA) was completely different from that shown by poly(BisGMA/TEGDMA). The difference is discussed in terms of diffusion coefficients. Initially, water advancing contact angles (theta(ADV)) were 75 degrees and 95 degrees, respectively. After I month in water both polymers showed a reduction of about 20 degrees in theta(ADV). In poly(Bis-GMA/TEGDMA), the reduction in theta(ADV) obey to water absorption and bulk plasticization; it showed a reduction of 15 degrees C in glass transition temperature, T-g. In contrast, the reduction in theta(ADV) in poly (Sil center dot Bis-GMA) obeyed to water adsorption and reorientation of the molecules at the surface in contact with the water phase; it only showed a change of 2 degrees C in T-g. Contact angle hysteresis provided further evidence about plasticization. According to our results poly(Sil center dot Bis-GMA) is more stable in water than poly(Bis-GMA/TEGDMA). (C) 2007 Wiley Periodicals, Inc.
机译:Bis-GMA(2,2-双-[4-(2-羟基-3-甲基丙烯酰氧基丙氧基)苯基]丙烷)是一种粘性吸湿性单体,可与三甘醇-二甲基丙烯酸酯(TEGDMA)一起用于牙齿修复。将Bis-GMA与二甲基-异丙基硅氧烷进行甲硅烷基化并进一步聚合,以提高耐水性和粘度。甲硅烷基化的单体Sil中心点Bis-GMA的粘度比母体单体的粘度低50倍。在水中放置1个月后,聚(Bis-GMA / TEGDMA)吸收了2.6%的水,而甲硅烷基化聚合物聚(Sil中心点Bis-GMA)仅吸收了0.56%。在此过程中,水从每种聚合物中提取出残留的单体。聚(Sil中心点Bis-GMA)中水的吸附和解吸行为随时间的变化与聚(BisGMA / TEGDMA)完全不同。根据扩散系数讨论差异。最初,水前进接触角(theta(ADV))分别为75度和95度。在水中放置1个月后,两种聚合物的theta(ADV)值均降低了约20度。在poly(Bis-GMA / TEGDMA)中,theta(ADV)的减少遵循吸水和本体增塑的要求;玻璃化转变温度T-g降低了15℃。相反,聚(Sil中心点Bis-GMA)中的theta(ADV)的减少遵循水的吸附和与水相接触的表面分子的重新取向;它的T-g仅变化了2摄氏度。接触角迟滞为塑化提供了进一步的证据。根据我们的结果,聚(Sil中心点Bis-GMA)在水中比聚(Bis-GMA / TEGDMA)更稳定。 (C)2007 Wiley期刊公司

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