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Biomechanical Effects of New Resin Matrix System on Dental Fiber-Reinforced Composites

机译:新型树脂基体系对牙科纤维增强复合材料的生物力学影响

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摘要

There are concerns that dental materials based on bis-phenol-A-glycidylmethacrylate (bis-GMA) may be hazardous. Alternative monomers such as 1,6-hexanediol dimethacrylate (HDDMA) is under research. This research aimed to determine the effect of resin matrix compositions on the biomechanical properties of E-glass fiber-reinforced composite (FRC) using bis-phenol-A-glycidylmethacrylate (bis-GMA), methylmethacrylate (MMA), 1.6-hexanediol dimethacrylate (HDDMA), camphorquinone (CQ) and N,N-cyanoethyl methylaniline (CEMA). The ratios of the resin matrices (weight %) were 78.4 % bis-GMA + 19.6 % MMA + 1 % CQ + 1 % CEMA (control-group), 78.4 % HDDMA + 19.6 % MMA + 1 % CQ + 1 % CEMA (EXP1-group) and 49 % HDDMA + 49 % MMA + 1 % CQ + 1 % CEMA (EXP2-group). E-glass fibers were embedded in matrix and light-cured for 3 x 40 s. Three-point bending (2 x 2 x 25) mm and Vicker's hardness (2 x 2 x 5) mm were examined (n = 6) by a universal testing machine (Torsee's UTM, Japan) and a micro-hardness tester (MTX70 Matsuzawa, Japan). The data were analyzed by ANOVA. Bending measurement revealed the mean value of control-group (674.1 + 9.9) MPa was higher than EXPl-group (638.1 ± 8.6) MPa and EXP2-group (448.3 + 7.8) MPa. The ANOVA showed significant difference in bending values among the groups (p < 0.05). Hardness measurement proved EXP1-group mean value (179.1 ± 2.5) VHN was higher than control-group (181.5 + 11.5) VHN and EXP2-group (168.2 + 7.9) VHN. The ANOVA proved there was significant difference (p < 0.05) in hardness values. In conclusion, a resin matrix system based on HDDMA-MMA (EXPl-group) showed comparable flexural strength and hardness properties to bis-GMA-MMA (control-group) system.
机译:人们担心基于双酚A-甲基丙烯酸缩水甘油酯(bis-GMA)的牙科材料可能很危险。替代性单体,如1,甲基丙烯酸1,6-己二醇酯(HDDMA)正在研究中。这项研究旨在确定树脂基质组合物对使用双酚A甲基丙烯酸缩水甘油酯(bis-GMA),甲基丙烯酸甲酯(MMA),1.6-己二醇二甲基丙烯酸酯(FRC)的E-玻璃纤维增​​强复合材料(FRC)的生物力学性能的影响。 HDDMA),樟脑醌(CQ)和N,N-氰基乙基甲基苯胺(CEMA)。树脂基质的比例(重量%)为78.4%bis-GMA + 19.6%MMA + 1%CQ + 1%CEMA(对照组),78.4%HDDMA + 19.6%MMA + 1%CQ + 1%CEMA( EXP1组)和49%HDDMA + 49%MMA + 1%CQ + 1%CEMA(EXP2组)。将电子玻璃纤维嵌入基质中并光固化3 x 40 s。用万能试验机(日本Torsee UTM公司)和显微硬度计(MTX70 Matsuzawa)检测(n = 6)三点弯曲(2 x 2 x 25)mm和维氏硬度(2 x 2 x 5)mm(n = 6) , 日本)。数据通过ANOVA分析。弯曲测量显示,对照组(674.1 + 9.9)MPa的平均值高于EXP1组(638.1±8.6)MPa和EXP2组(448.3 + 7.8)MPa。方差分析显示各组之间的弯曲值存在显着差异(p <0.05)。硬度测量证明,EXP1组平均值(179.1±2.5)VHN高于对照组(181.5 + 11.5)VHN和EXP2组(168.2 + 7.9)VHN。方差分析证明硬度值存在显着差异(p <0.05)。总之,基于HDDMA-MMA(EXP1组)的树脂基体体系显示出与bis-GMA-MMA(对照组)体系相当的抗弯强度和硬度性能。

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