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A new kinetic model for the photopolymerization shrinkage-strain of dental composites and resin-monomers

机译:牙科复合材料和树脂单体光聚合收缩应变的新动力学模型

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Objectives. The aim of the study was to develop a new kinetic model for the shrinkage-strain rates of dental resin composites. The effect of filler content on the shrinkage-strain kinetics and degree of conversion of dental composites was also investigated. Methods. A resin matrix containing 65 wt.% Bis-GMA and 35 wt.% TEGDMA was prepared. 0.5 wt.% camphorquinone and 0.5 wt.% dimethyl aminoethyl methacrylate were dissolved in the resin as photo-initiator system. Silanized glass fillers were added in different percentages to the resin-monomers. The shrinkage-strain of the specimens photopolymerized at circa 550 mW/cm~2 was measured using the bonded-disc technique at 23, 37 and 45℃ for the matrix monomers and 23℃ for the composites. Initial shrinkage-strain rates were obtained by numerical differentiation of shrinkage-strain data with respect to time. Degree-of-conversion of the composites containing different filler contents was measured using FTIR spectroscopy. Results. A new kinetic model was developed for the shrinkage-strain rate using the auto-catalytic model of Kamal [Kamal MR, Sourour S. Kinetic and thermal characterization of thermoset cure. Polym Eng Sci 1973;13(1):59-64], which is used to describe the reaction kinetics of thermoset resins. The model predictions were in good agreement with the experimental data. The results also showed a linear correlation between the shrinkage-strain (and shrinkage-strain rate) and filler-volume fraction. The filler fraction did not affect the degree-of-conversion of the composites. Significance. The rate of polymerization, determined via the shrinkage, being invariant with filler-fraction, suggests that only a relatively high filler-surface area, as may be obtained with nano-fillers, will affect the network-forming kinetics of the resin matrix.
机译:目标。该研究的目的是为牙科树脂复合材料的收缩应变率建立一个新的动力学模型。还研究了填料含量对牙科复合材料的收缩应变动力学和转化度的影响。方法。制备包含65重量%的Bis-GMA和35重量%的TEGDMA的树脂基质。将0.5重量%的樟脑醌和0.5重量%的甲基丙烯酸二甲基氨基乙基酯溶解在树脂中作为光引发剂体系。将硅烷化玻璃填料以不同百分比添加到树脂单体中。使用粘结圆盘技术分别在23、37和45℃下对基体单体和23℃下的复合材料分别进行了550 mW / cm〜2的光致聚合试样的收缩应变测量。通过相对于时间的收缩应变数据的数值微分获得初始收缩应变率。使用FTIR光谱法测量包含不同填料含量的复合材料的转化度。结果。使用Kamal [Kamal MR,Sourour S.的热催化动力学和热表征]的自动催化模型,开发了收缩率的新动力学模型。 Polym Eng Sci 1973; 13(1):59-64],其用于描述热固性树脂的反应动力学。模型预测与实验数据吻合良好。结果还表明收缩率(和收缩率)与填料体积分数之间存在线性关系。填料分数不影响复合材料的转化率。意义。通过收缩率确定的聚合速率随填料分数而变化,这表明,只有相对较高的填料表面积(如纳米填料可能获得的)才会影响树脂基体的网络形成动力学。

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