前往化源商城

Odontology 2015-05-01

Influence of the base and diluent monomer on network characteristics and mechanical properties of neat resin and composite materials.

Nívea Regina de Godoy Fróes-Salgado, Vinícius Gajewski, Bárbara Pick Ornaghi, Carmem Silvia Costa Pfeifer, Marcia Margarete Meier, Tathy Aparecida Xavier, Roberto Ruggiero Braga

文献索引:Odontology 103 , 160-8, (2015)

全文:HTML全文

摘要

This study evaluated the effect of the combination of two dimethacrylate-based monomers [bisphenol A diglycidyl dimethacrylate (BisGMA) or bisphenol A ethoxylated dimethacrylate (BisEMA)] with diluents either derived from ethylene glycol dimethacrylate (ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, tetraethylene glycol dimethacrylate) or 1,10-decanediol dimethacrylate (D3MA) on network characteristics and mechanical properties of neat resin and composite materials. The degree of conversion, maximum rate of polymerization and water sorption/solubility of unfilled resins and the flexural strength and microhardness of composites (after 24 h storage in water and 3 months storage in a 75 vol% ethanol aqueous solution) were evaluated. Data were analyzed with two-way ANOVA and Tukey's test (α = 0.05). The higher conversion and lower water sorption presented by BisEMA co-polymers resulted in greater resistance to degradation in ethanol compared with BisGMA-based materials. In general, conversion and mechanical properties were optimized with the use of long-chain dimethacrylate derivatives of ethylene glycol. D3MA rendered more hydrophobic materials, but with relatively low conversion and mechanical properties.

相关化合物

结构式 名称/CAS号 全部文献
3-(甲基丙烯酰氧)丙基三甲氧基硅烷 结构式 3-(甲基丙烯酰氧)丙基三甲氧基硅烷
CAS:2530-85-0
双酚a 结构式 双酚a
CAS:80-05-7
四乙二醇二甲基丙烯酸酯 结构式 四乙二醇二甲基丙烯酸酯
CAS:109-17-1