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具有不同基体单体比例的E玻璃纤维复合材料模型的特性

Properties of model E-glass fiber composites with varying matrix monomer ratios.

作者信息

Alshabib Abdulrahman, Silikas Nikolaos, Watts David C

机构信息

Department of Restorative Dentistry, College of Dentistry, King Saud University, Riyadh, Saudi Arabia.

Dentistry, School of Medical Sciences, University of Manchester, Manchester, UK.

出版信息

Dent Mater. 2024 Mar;40(3):441-450. doi: 10.1016/j.dental.2023.12.002. Epub 2023 Dec 21.

Abstract

OBJECTIVE

To evaluate properties of fiber-reinforced-composites (FRC) containing Bis-EMA/UDMA monomers but identical dispersed phase (60% wt BaSi glass power +10% wt E-glass fibre).

METHODS

A control (Group A), monomer mixture comprising 60% Bis-GMA, 30% TEGDMA, and 10% PMMA (typical FRC monomers) was used. The following monomer mass fractions were mixed: 50% bis-GMA plus 50% of different ratios of Bis-EMA+UDMA to produce consistent formulations (Groups B-E) of workable viscosities was also studied. Flexural strength (FS), fracture toughness (K), water sorption (SP), solubility (SL) and hygroscopic expansion (HE) were measured. FS and K specimens were stored for 1, 7 d, and 30 d in water at 37 °C. SP/SL specimens were water-immersed for 168d, weighed at intervals, then dried for 84 d at 37 °C. To analyze differences in FS, and K, a two-way ANOVA and Tukey post-hoc tests (α = 0.05) were conducted. For SP/SL, and HE, one-way ANOVA with subsequent Tukey post-hoc tests (α = 0.05) were utilized.

RESULTS

FS and K for groups A, D, E decreased progressively after 1 d. Groups B and C (highest amounts of Bis-EMA) did not decrease significantly. The modified matrix composites performed significantly better than the control group for SP and HE. The control group outperformed the experimental composites only for SL with up to 250% higher SL for group E (6.9 μg/mm) but still below the maximum permissible threshold of 7.5 μg/mm.

SIGNIFICANCE

EXPERIMENTAL: composites with highest amounts of Bis-EMA showed improved hydrolytic stability and overall enhancement in several clinically-relevant properties. This makes them potential candidates for alternative matrices to a semi-interpenetrating network in fiber-reinforced composites.

摘要

目的

评估含有双甲基丙烯酸乙二酯/二甲基丙烯酸脲烷单体但分散相相同(60%重量的硅酸钡玻璃粉+10%重量的E玻璃纤维)的纤维增强复合材料(FRC)的性能。

方法

使用一种对照物(A组),即由60%双酚A双甲基丙烯酸缩水甘油酯、30%三乙二醇二甲基丙烯酸酯和10%聚甲基丙烯酸甲酯(典型的FRC单体)组成的单体混合物。还研究了以下单体质量分数的混合情况:50%双酚A双甲基丙烯酸缩水甘油酯加上50%不同比例的双甲基丙烯酸乙二酯+二甲基丙烯酸脲烷,以制备具有可行粘度的一致配方(B-E组)。测量了弯曲强度(FS)、断裂韧性(K)、吸水性(SP)、溶解度(SL)和吸湿膨胀(HE)。FS和K试样在37℃水中储存1天、7天和30天。SP/SL试样在水中浸泡168天,定期称重,然后在37℃下干燥84天。为了分析FS和K的差异,进行了双向方差分析和Tukey事后检验(α=0.05)。对于SP/SL和HE,使用了单向方差分析及随后的Tukey事后检验(α=0.05)。

结果

A组、D组和E组的FS和K在1天后逐渐下降。B组和C组(双甲基丙烯酸乙二酯含量最高)没有显著下降。改性基体复合材料在SP和HE方面的表现明显优于对照组。对照组仅在SL方面优于实验复合材料,E组的SL高达6.9μg/mm,比对照组高250%,但仍低于7.5μg/mm的最大允许阈值。

意义

实验性:双甲基丙烯酸乙二酯含量最高的复合材料显示出改善的水解稳定性以及几种临床相关性能的整体增强。这使其成为纤维增强复合材料中半互穿网络替代基体的潜在候选材料。

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