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Nylon 6/SiO2 nanocomposites synthesized by in situ anionic polymerization

机译:原位阴离子聚合合成尼龙6 / SiO2纳米复合材料。

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In situ anionic polymerization of epsilon-caprolactam in the presence Of SiO2 and silanated SiO2 nanoparticles was promoted as a route for the synthesis of two series of nylon 6/SiO2 nanocomposites. The process was performed at 160 degrees C well below the melting temperature of the nylon 6 (T-m similar to 225 degrees C) and initiated/activated with sodium dicaprolactamato-bis(2-methoxyethoxo)aluminate/N,N'-[methylene-di(4,4'-phenylene)bis-carbamoyl]bis-epsilon-caprolactam system. The nanocomposites obtained exhibit higher onset decomposition temperatures than neat nylon 6 and a tendency of reduction of the polymer yields, degree of polymerization, water absorption and melting temperatures with silica content increasing. The crystallization temperature, T-c of the nanocomposites reaches a maximum value at 2.0 wt.% of the nanoparticles. The mechanical tests of nanocomposites revealed an increase in flexural modulus as a function of filler percentage and a decrease in notched impact strength by addition of the modified silica (over 4.0 wt.%) and unmodified silica. Furthermore, the flexural strength diminishes both the treated and untreated filler content is increased for concentration of > 4.0 wt.%.
机译:SiO 2和硅烷化的SiO 2纳米颗粒存在下,ε-己内酰胺的原位阴离子聚合反应被促进为合成尼龙6 / SiO 2纳米复合材料的两种途径。该过程在160°C远低于尼龙6的熔融温度(Tm类似于225°C)下进行,并用二己内酰胺基双-(2-甲氧基乙氧基)铝酸钠/ N,N'-[亚甲基-di (4,4′-亚苯基)双氨基甲酰基]双ε-己内酰胺体系。所获得的纳米复合材料显示出比纯尼龙6更高的起始分解温度,并且随着二氧化硅含量的增加,聚合物产率,聚合度,吸水率和熔融温度降低的趋势。纳米复合材料的结晶温度T-c在纳米颗粒的2.0重量%处达到最大值。纳米复合材料的机械测试表明,通过添加改性二氧化硅(超过4.0 wt%)和未改性二氧化硅,挠曲模量随填料百分比的增加而缺口冲击强度降低。此外,对于> 4.0重量%的浓度,弯曲强度减小了处理的和未处理的填料含量。

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