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Optical characterization of bisphenol-A-glycidyldimethacrylate-triethyleneglycoldimethacrylate (BisGMA/TEGDMA) monomers and copolymer

机译:双酚-A-二甲基丙烯酸缩水甘油酯-三亚乙基甘油二甲基丙烯酸酯(BisGMA / TEGDMA)单体和共聚物的光学表征

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Objectiue. The fundamental optical characteristics of dental polymers as a function of curing time are exiguously reported in the literature. In this work the refractive index [1] and the extinction coefficient [2] of bisphenol-A-glycidyldimethacrylate-triethyleneglycoldimethacrylate (BisGMA/TEGDMA)-based polymers of different volume fractions have been studied as a function of the curing time. A comparison between the measured index of refraction and theoretical calculation based on molar refraction is made. Also the temporal behavior of both the refractive index and extinction coefficient is compared. Methods. Index of refraction: BisGMA/TEGDMA monomer samples were cured with a commercial light-curing unit by using camphorquinone and DMAEMA as the photoini-tiator system. Curing times of 0, 40, 60, 300, 900 and 1800 s were used. The refractive indices were determined with a refractometer at 470 nm wavelength, where the peak absorption of the camphorquinone photoinitiator is located. Extinction coefficient: BisGMA/TEGDMA samples having different lengths were cured and the relative attenuation of light at 470 nm was measured as a function of the curing time (0, 40, 60, 300, 900, 1800 s). Results. The results show that in general the index of refraction increases during the pho-topolymerization process in a time frame from 0 to 40 s and then approaches a steady-state value, which depends on the original composition of the admixture. The detailed refractive index change depends on the volume fractions of the constituent substances. The extinction coefficient decreases in a time frame from 60 to 900 s and reaches a steady-state value thereafter. Significance. Knowledge of the fundamental optical characteristics of commonly used dental polymers is essential in the development of advanced light-initiated curing methods.
机译:反对牙科聚合物基本的光学特性随固化时间的变化在文献中已有报道。在这项工作中,已经研究了不同体积分数的双酚-A-缩水甘油基二甲基丙烯酸酯-三亚乙基甘油二甲基丙烯酸酯(BisGMA / TEGDMA)基聚合物的折射率[1]和消光系数[2]与固化时间的关系。将测得的折射率与基于摩尔折射率的理论计算进行了比较。还比较了折射率和消光系数的时间行为。方法。折射率:BisGMA / TEGDMA单体样品通过使用樟脑醌和DMAEMA作为光引发剂体系,通过商用光固化装置进行固化。固化时间为0、40、60、300、900和1800 s。折射率是用折射计在470 nm波长处测定的,樟脑醌光引发剂的吸收峰位于此位置。消光系数:固化具有不同长度的BisGMA / TEGDMA样品,并根据固化时间(0、40、60、300、900、1800 s)测量470 nm处的光的相对衰减。结果。结果表明,一般而言,在光聚合过程中,折射率在0到40 s的时间范围内增加,然后接近稳态值,这取决于混合物的原始组成。详细的折射率变化取决于组成物质的体积分数。消光系数在60到900 s的时间范围内减小,此后达到稳态值。意义。在开发先进的光引发固化方法时,必须了解常用牙科聚合物的基本光学特性。

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