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Synthesis and Characterization of PMMA/SiO_2 Nanocomposites by In Situ Suspension Polymerization

机译:原位悬浮聚合法合成PMMA / SiO_2纳米复合材料及其表征

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摘要

Poly(methyl methacrylate) (PMMA)/SiO_2 nanocomposites were prepared by in situ suspension polymerization. Two types of modified methods were used to modify nano-SiO2: one was modification by c-methacyloxypropyl trimethoxy silane (KH570) and lauryl alcohol (12COH) while the other was grafting PMMA onto the surface of KH570 treated SiO2. Transmission electron microscopy (TEM) and Fourier transformed infrared (FTIR) were used to characterize the structures of the nanocomposites. The influence of synthetic conditions, for instance, surface modification, initial SiO2 contents and reaction temperature, on the microsphere’s size and molecular weight of the extracted PMMA were studied by gel permeation chromatograph (GPC) and optical microscopy (OM) in details. Thermal property of the nanocomposites was investigated by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The results indicate that the presence and content of SiO2 have a vital effect on the shape and size of the nanocomposite microspheres, as well as molecular weight of the extracted PMMA. Grafting polymer to the surface of SiO2 is an effective way for the purpose of effective in situ suspension polymerization. Compared to pure PMMA, the thermal properties of the nanocomposites were improved.
机译:通过原位悬浮聚合制备了聚甲基丙烯酸甲酯(PMMA)/ SiO_2纳米复合材料。两种类型的改性方法用于改性纳米SiO2:一种是通过c-甲酰氧基丙基三甲氧基硅烷(KH570)和月桂醇(12COH)进行改性,而另一种是将PMMA接枝到KH570处理过的SiO2表面上。透射电子显微镜(TEM)和傅立叶变换红外(FTIR)用于表征纳米复合材料的结构。通过凝胶渗透色谱(GPC)和光学显微镜(OM)详细研究了合成条件,例如表面改性,SiO2初始含量和反应温度对提取的PMMA微球尺寸和分子量的影响。通过热重分析(TGA)和差示扫描量热法(DSC)研究了纳米复合材料的热性能。结果表明,SiO 2的存在和含量对纳米复合微球的形状和尺寸以及所提取的PMMA的分子量具有至关重要的影响。为了有效地原位悬浮聚合,将聚合物接枝到SiO 2表面是有效的方法。与纯PMMA相比,纳米复合材料的热性能得到了改善。

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