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Effects of Different Silane Coupling Agent Monomers on Flexural Strength of an Experimental Filled Resin Composite

机译:不同硅烷偶联剂单体对实验填充树脂复合材料抗弯强度的影响

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摘要

The hydrolytic stability of various silane combinations and their effects on biomechanical properties and water sorption of an experimental dental composite made of bis-GMA and TEGDMA and silane-treated fillers were evaluated. Four silane coupling agents and their blends with a cross-linker silane were used as coupling agents for the 0.7-um BaSiO3 fillers. The silanization was carried out in toluene containing 1% (v/v) of one of the four following organofunctional silane coupling agents: 3-acryloxypropyltrimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-styrylethylttimethoxysilane and 3-isocyanatopropyltriethoxysilane. Blends of these functional silanes with 1% (v/v) of a cross-linker silane, 1,2-bis-(triethoxysilyl)ethane were also used for silanization. Composites were prepared by mixing 5.00 g Ba-glass filler with 2.00 g of a resin mixture consisting of bis-GMA (58.8 wt%) and TEGDMA (39.2 wt%) in a high-speed mixer. Three-point bending test specimens (2.0 mm x 2.0 mm x 25.0 mm) were fabricated (n = 8) in a mould and photo-polymerized. The degree of conversion was measured with FT-IR. Biomechanical testing was carried out according to the ISO 10477 standard. Specimens were tested (flexural strength) after 30 days of water storage (37°C, distilled water). Water sorption and solubility (in wt%) were also measured on 1, 2, 3, 5, 7, 14, 21 and 30 days in water storage. Statistical analysis with ANOVA showed that the highest flexural strength was obtained when 3-acryloxypropyltrimethoxysilane + 1,2-bis-(triethoxysilyl)ethane (100.5 MPa; SD, 25.7 MPa) was used in the silanization step, and the lowest was obtained when 3-isocyanatopropyltriethoxysilane + 1,2-bis-(triethoxysilyl)ethane (28.9 MPa; SD, 8.8 MPa) was used. The three-point bending strength was significantly affected by the functionality of the main silane tested (p < 0.05), but not by the addition of the cross-linker silane (p > 0.05). The composite that had been silanized with 3-isocyanatopropyltriethoxysilane had the greatest amount of water uptake (1.75%), and the composite silanized with 3-methacryloxypropyltrimethoxysilane + 1,2-bis-(triethoxysilyl)ethane had the least (1.08%). In conclusion, selection of the functional silane monomer can be a significant factor in developing filled resin composites in dentistry.
机译:评估了各种硅烷组合的水解稳定性及其对由bis-GMA和TEGDMA制成的实验牙科复合材料以及经过硅烷处理的填料的生物力学性能和吸水率的影响。四种硅烷偶联剂及其与交联剂硅烷的共混物用作0.7um BaSiO3填料的偶联剂。硅烷化反应是在含有1%(v / v)的以下四种有机官能硅烷偶联剂之一的甲苯中进行的:3-丙烯酰氧基丙基三甲氧基硅烷,3-甲基丙烯酰氧基丙基三甲氧基硅烷,3-苯乙烯基乙基叔甲氧基硅烷和3-异氰基丙基丙基三乙氧基硅烷。这些官能硅烷与1%(v / v)的交联剂硅烷1,2-双(三乙氧基甲硅烷基)乙烷的共混物也用于硅烷化。通过在高速混合器中将5.00 g Ba-玻璃填料与2.00 g由bis-GMA(58.8 wt%)和TEGDMA(39.2 wt%)组成的树脂混合物混合来制备复合材料。在模具中制作三点弯曲试样(2.0毫米x 2.0毫米x 25.0毫米)(n = 8)并进行光聚合。用FT-IR测量转化度。根据ISO 10477标准进行了生物力学测试。储水(37°C,蒸馏水)30天后测试样品(抗弯强度)。还在储水的1、2、3、5、7、14、21和30天测量了吸水率和溶解度(以重量%计)。通过ANOVA进行的统计分析表明,在硅烷化步骤中使用3-丙烯酰氧基丙基三甲氧基硅烷+ 1,2-双-(三乙氧基甲硅烷基)乙烷(100.5 MPa; SD,25.7 MPa)可获得最高的挠曲强度,而当3时则获得最低的挠曲强度。使用-异氰酸根合丙基三乙氧基硅烷+ 1,2-双-(三乙氧基甲硅烷基)乙烷(28.9 MPa; SD,8.8 MPa)。三点弯曲强度受测试的主要硅烷的功能性(p <0.05)显着影响,但不受交联剂硅烷的添加(p> 0.05)的影响。用3-异氰酸根合丙基三乙氧基硅烷硅烷化的复合材料的吸水量最大(1.75%),而用3-甲基丙烯酰氧基丙基三甲氧基硅烷+ 1,2-双-(三乙氧基甲硅烷基)乙烷硅烷化的复合材料的吸水率最低(1.08%)。总之,官能硅烷单体的选择可能是开发牙科用填充树脂复合材料的重要因素。

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