首页> 外文期刊>Journal of Applied Polymer Science >Synthesis of polycarbonate-silica nanocomposites from copolymerizationof CO2 with allyl glycidyl ether, cyclohexene oxide, and sol-gel
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Synthesis of polycarbonate-silica nanocomposites from copolymerizationof CO2 with allyl glycidyl ether, cyclohexene oxide, and sol-gel

机译:CO2与烯丙基缩水甘油醚,环氧环己烯和溶胶-凝胶的共聚反应合成聚碳酸酯-二氧化硅纳米复合材料

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The copolymerization of carbon dioxide, allyl glycidyl ether, and cyclohexene oxide catalyzed by the system consisting of Y(CF3CO2)(3) Zn(Et)(2), and pyrogallol in the solvent of 1, 3-dioxolane was performed in this study. The IR, H-1 NMR, and C-13-NMR spectra, as well as the elemental analysis, indicated that the resulting copolymer was an alternating polycarbonate possessing more than 90% of carbonate units. The molecular weight could be as high as 1.5 X 10(5), and the polydispersity index was 4.5. The resultant polycarbonate was found to effectively react with 3-(trimethoxysilyl)propyl methacrylate via a free radical reaction to result in a precursor used in the sol-gel process to synthesize a polycarbonate-silica nanocomposite. The nanocomposites were characterized by SEM, Si-29 NMR, TGA, DSC, and UV-Vis. Silica particles with size less than 100 nm were found to disperse uniformly in the nanocomposites. It was also found that the thermal properties were dependent on the content of cyclohexene carbonate units. Both the thermal and mechanical properties of the resultant nanocomposites could be adjusted with silica content, while the transparency was comparable to the base copolymer even at high silica contents. (c) 2005 Wiley Periodicals, Inc.
机译:在本研究中,由Y(CF3CO2)(3)Zn(Et)(2)和邻苯三酚在1,3-二氧戊环溶剂中催化的二氧化碳,烯丙基缩水甘油醚和环己烯的共聚合反应。 IR,H-1 NMR和C-13-NMR光谱以及元素分析表明,所得共聚物是具有超过90%碳酸酯单元的交替聚碳酸酯。分子量可高达1.5 X 10(5),多分散指数为4.5。发现所得的聚碳酸酯可通过自由基反应与甲基丙烯酸3-(三甲氧基甲硅烷基)丙酯有效反应,从而导致在溶胶-凝胶法中用于合成聚碳酸酯-二氧化硅纳米复合材料的前体。通过SEM,Si-29 NMR,TGA,DSC和UV-Vis对纳米复合材料进行了表征。发现尺寸小于100nm的二氧化硅颗粒均匀地分散在纳米复合材料中。还发现热性能取决于碳酸环己烯单元的含量。可以用二氧化硅含量调节所得纳米复合材料的热性能和机械性能,而即使在高二氧化硅含量下,透明度也可与基础共聚物相比。 (c)2005年Wiley Periodicals,Inc.

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