Laboratory of Organic Chemical Technology, Department of Chemistry, Aristotle University of Thessaloniki, Thessaloniki GR-54124, Greece.
Dent Mater. 2011 Nov;27(11):1144-52. doi: 10.1016/j.dental.2011.08.008. Epub 2011 Sep 13.
The purpose of this work was the study of the effect of the amount of a urethane dimethacrylate silane (UDMS) coupling agent on physical properties of dental light-cured resin nanocomposites based on Bis-GMA/TEGDMA (50/50 wt/wt) matrix and Aerosil OX50 as filler.
Silica nanoparticles (Aerosil OX 50) used as filler were silanized with 5 different amounts of UDMS 1.0, 2.5, 5.0, 7.5 and 10 wt% relative to silica. The silanizated silica nanoparticles were identified by FT-IR spectroscopy and thermogravimetric analysis (TGA). Then the silanized nanoparticles (60 wt%) were mixed with a Bis-GMA/TEGDMA (50/50 wt/wt) matrix. Degree of conversion of light cured composites was determined by FT-IR analysis. The static flexural strength and flexural modulus were measured using a three-point bending set up. The dynamic thermomechanical properties were determined by DMA analyzer. Measurements were taken in samples stored, immediately after curing, in water at 37°C for 24 h. Sorption, solubility and volumetric change were determined after storage of composites in water or ethanol/water of 75 vol% for 30 days. Thermogravimetric analysis of composites was performed in nitrogen atmosphere from 50 to 800°C.
Almost all of used amount of silane remained chemically bounded on the surface of silica particles, forming a layer around them, which have dense accumulation of methacrylate groups. No significant statistic difference was found to exist between the degree of conversion values of composites with different silane contents. The composite with the lowest amount of UDMS (1.0 wt%) showed the lower flexural strength value, the higher static and dynamic elastic modulus values and the higher sorbed liquid value and solubility.
The optimum concentration of UDMS seems to be that of 2.5 wt%. Higher concentrations of UDMS did not improve the properties of composites.
本工作研究了一种氨丙基甲基二乙氧基硅烷(UDMS)偶联剂的用量对双酚 A 二甲基丙烯酸酯/三乙二醇二甲基丙烯酸酯(50/50wt/wt)基质和 Aerosil OX50 为填料的光固化树脂纳米复合材料物理性能的影响。
使用 5 种不同量的 UDMS(相对于二氧化硅分别为 1.0、2.5、5.0、7.5 和 10wt%)对作为填料的二氧化硅纳米粒子(Aerosil OX50)进行硅烷化。通过傅里叶变换红外光谱(FT-IR)和热重分析(TGA)对硅烷化的二氧化硅进行了鉴定。然后将硅烷化的纳米粒子(60wt%)与双酚 A 二甲基丙烯酸酯/三乙二醇二甲基丙烯酸酯(50/50wt/wt)基质混合。通过 FT-IR 分析测定光固化复合材料的转化率。使用三点弯曲装置测量静态弯曲强度和弯曲模量。通过 DMA 分析仪测定动态热机械性能。在固化后立即将样品在 37°C 的水中储存 24 小时后进行测量。在水中或 75vol%乙醇/水储存 30 天后,测定复合材料的溶胀、溶解度和体积变化。在氮气气氛下,从 50 到 800°C 对复合材料进行热重分析。
几乎所有使用量的硅烷都化学结合在二氧化硅颗粒表面,形成一层围绕它们的致密甲基丙烯酰基堆积层。具有不同硅烷含量的复合材料的转化率值之间没有发现存在显著的统计学差异。含有最低量 UDMS(1.0wt%)的复合材料表现出较低的弯曲强度值、较高的静态和动态弹性模量值以及较高的吸液值和溶解度。
UDMS 的最佳浓度似乎为 2.5wt%。更高浓度的 UDMS 并没有改善复合材料的性能。