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Synthesis and physicochemical investigation of imide-functionalized silica nanocomposites

机译:酰亚胺官能化二氧化硅纳米复合材料的合成与物理化学研究

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摘要

The incorporation of inorganic nanoparticles into polymers have gained significant attention to improving functional properties. The ultimate nanocomposite behaviors are influenced by many parameters, such as microstructural distribution that are produced during the treatment process. Herein, a hybrid material integrating a modified network into a polyimide PI matrix was produced via the sol-gel method by the reaction of pyromellitic dianhydride, 4, 4-oxydianaline, and 1, 5-diaminonaphthalene to synthesize copolyimides nanocomposite. The modified polyimide and unmodified polyimide silica (SiO2) nanoparticles were incorporated in the polyimide matrix to have polyimide silica nanocomposite. In modified silica nanoparticles, 3-aminopropyltriethosilane was introduced to have better compatibility among inorganic-organic hybrid with similar chemical contact due to their flexible alkyl group. The surface morphology or structure of silica and polyimide was affirmed by scanning electron microscopy, Fourier transforms infrared spectroscopy confirmed the synthesis of pure polyimide, unmodified polyimide, and modified polyimide silica via presence and absence of certain peaks. Thermogravimetric analysis (TGA) results showed high thermal stability of nanocomposites as silica content increases. In contrast to unmodified silica, the modified silica provides more thermal stability to the nanocomposites. Dynamic mechanical analysis was used to investigate the tensile stress of pure polyimide, unmodified, and modified silica nanocomposites. Thermal stability, storage modulus, and moisture absorption of these hybrid materials were improved with silica nanoparticles. The TG mass spectrum confirms the successful synthesis of modified silica networks. The substituted silica nanoparticles show higher mechanical toughness and storage in modified compared to unmodified silica nanocomposite, which exhibits stronger binding attraction between silica nanoparticles and polyimide matrix.
机译:无机纳米颗粒在聚合物中的应用已经引起了人们对改善功能特性的极大关注。最终的纳米复合材料行为受许多参数的影响,例如处理过程中产生的微观结构分布。在此,通过均苯四甲酸二酐、4,4-氧二苯胺和1,5-二氨基萘的反应,通过溶胶-凝胶方法制备了将改性网络整合到聚酰亚胺PI基体中的杂化材料,以合成共聚酰亚胺纳米复合材料。将改性的聚酰亚胺和未改性的聚酰亚胺-二氧化硅(SiO2)纳米颗粒并入聚酰亚胺基体中以获得聚酰亚胺-二氧化硅纳米复合材料。在改性二氧化硅纳米颗粒中,3-氨丙基三乙硅烷由于其柔性烷基而被引入到具有相似化学接触的无机-有机杂化物中,以具有更好的相容性。扫描电子显微镜证实了二氧化硅和聚酰亚胺的表面形态或结构,傅里叶变换红外光谱证实了通过存在和不存在某些峰来合成纯聚酰亚胺、未改性聚酰亚胺和改性聚酰亚胺二氧化硅。热重分析(TGA)结果表明,随着二氧化硅含量的增加,纳米复合材料具有较高的热稳定性。与未改性二氧化硅相比,改性二氧化硅为纳米复合材料提供了更高的热稳定性。动态力学分析用于研究纯聚酰亚胺、未改性和改性二氧化硅纳米复合材料的拉伸应力。二氧化硅纳米颗粒改善了这些杂化材料的热稳定性、储能模量和吸湿性。TG质谱证实了改性二氧化硅网络的成功合成。与未改性的二氧化硅纳米复合材料相比,经改性的二氧化硅纳米复合材料表现出更高的机械韧性和在改性的二氧化硅纳米复合材料中的存储能力,从而表现出二氧化硅纳米颗粒与聚酰亚胺基体之间更强的结合吸引力。

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