用液体橡胶和官能团改性二氧化硅表面用于新型聚烯烃基介电纳米复合材料

R. Anyszka, Xiaozhen He, Amirhossein Mahtabani, I. Rytöluoto, Eetta Saarimäki, K. Lahti, M. Paajanen, W. Dierkes, A. Blume
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引用次数: 0

摘要

提出了一种用于聚烯烃基介电复合材料的纳米二氧化硅表面改性的新型杂化方法。气相纳米二氧化硅被液体橡胶的长低聚链修饰,通过聚氨酯键连接到二氧化硅表面,增加了与基体的相容性。此外,为了改变二氧化硅的电荷捕获特性,还接枝了二级氨基硅烷。在聚丙烯/聚乙烯-共辛烯(PP/POE)共混体系中,长低聚链为纳米二氧化硅提供了良好的分散性,而氨基硅烷的加入降低了纳米二氧化硅的电荷捕获密度,同时增加了电荷捕获深度,从而影响了纳米二氧化硅的电荷捕获性能。扫描电子显微镜和差示扫描量热法显示,二氧化硅优选位于PP相,很可能是由于其与POE相比粘度较低。在PP相结晶温度显著升高的情况下,二氧化硅颗粒表现出明显的成核效应,特别是在进行二氧化硅表面处理时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Silica surface modification with liquid rubbers & functional groups for new polyolefin-based dielectric nano-composites
A novel hybrid approach for surface modification of nano-silica for polyolefin-based dielectric composites is presented. A fumed nano-silica was modified with long oligomeric chains of a liquid rubber, connected via urethane bonds to the silica surface increasing the compatibility with the matrix. Additionally, a secondary amino-silane was grafted in order to alter the charge trapping properties of the silica. The long oligomeric chains provide good dispersibility of the nanosilica in polypropylene/poly(ethylene-co-octene) (PP/POE) blends, while the functional urethane group along with a secondary amino-silane affected the charge trapping properties of the nano-composites by reducing the charge traps density and simultaneously increasing their depth. Scanning Electron Microscopy along with Differential Scanning Calorimetry revealed that the silica is preferably located in the PP phase, most likely due to its lower viscosity in comparison to POE. The silica particles exhibit a nucleating effect visible in a noticeable increase of the crystallization temperature of the PP phase, especially when the silica surface treatment is performed.
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