Surface modification of inorganic nanoparticles for development of organic–inorganic nanocomposites—A review

表面改性 纳米复合材料 聚合物 纳米颗粒 材料科学 聚合物纳米复合材料 硅烷 化学工程 粒子(生态学) 纳米技术 复合材料 工程类 海洋学 地质学
作者
Sarita Kango,Susheel Kalia,Annamaria Celli,James Njuguna,Youssef Habibi,Rajesh Kumar
出处
期刊:Progress in Polymer Science [Elsevier]
卷期号:38 (8): 1232-1261 被引量:1855
标识
DOI:10.1016/j.progpolymsci.2013.02.003
摘要

Nanoparticles and nanocomposites are used in a wide range of applications in various fields, such as medicine, textiles, cosmetics, agriculture, optics, food packaging, optoelectronic devices, semiconductor devices, aerospace, construction and catalysis. Nanoparticles can be incorporated into polymeric nanocomposites. Polymeric nanocomposites consisting of inorganic nanoparticles and organic polymers represent a new class of materials that exhibit improved performance compared to their microparticle counterparts. It is therefore expected that they will advance the field of engineering applications. Incorporation of inorganic nanoparticles into a polymer matrix can significantly affect the properties of the matrix. The resulting composite might exhibit improved thermal, mechanical, rheological, electrical, catalytic, fire retardancy and optical properties. The properties of polymer composites depend on the type of nanoparticles that are incorporated, their size and shape, their concentration and their interactions with the polymer matrix. The main problem with polymer nanocomposites is the prevention of particle aggregation. It is difficult to produce monodispersed nanoparticles in a polymer matrix because nanoparticles agglomerate due to their specific surface area and volume effects. This problem can be overcome by modification of the surface of the inorganic particles. The modification improves the interfacial interactions between the inorganic particles and the polymer matrix. There are two ways to modify the surface of inorganic particles. The first is accomplished through surface absorption or reaction with small molecules, such as silane coupling agents, and the second method is based on grafting polymeric molecules through covalent bonding to the hydroxyl groups existing on the particles. The advantage of the second procedure over the first lies in the fact that the polymer-grafted particles can be designed with the desired properties through a proper selection of the species of the grafting monomers and the choice of grafting conditions.
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