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Acrylate hybrid nanocomposite coatings based on SiO2 nanoparticles. In-situ semi-batch emulsion polymerization

机译:基于SiO2纳米粒子的丙烯酸酯杂化纳米复合涂料。原位半间歇乳液聚合

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摘要

Acrylate-SiO2 nanocomposites were synthesized by in situ emulsion semi-batch polymerization in aqueous dispersion utilizing untreated nanoparticles. Butyl acrylate (BA), methyl methacrylate (MMA) and acrylic acid (AA) with composition 56:42:2 were copolymerized at 50% solids in the presence of SiO2 nanoparticles of 7 nm size. SiO2 nanoparticles were added up to 3 wt% and the emulsions thus obtained were stable for at least 6 months in storage at room temperature. The semi-batch polymerization was carried out for 2.5 h. and yielded conversions as high as 92% and not lower than 84%, superior to batch polymerization of the same system. The synthesized emulsion hybrids were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, differential scanning calorimetry, scanning and transmission electron microscopy and atomic force microscopy. As cast films about 1 mm thick were optically transparent suggesting good nanoparticle dispersion. However, dispersed SiO2 nano aggregates were detected by SEM, TEM and AFM, and the identity of the nanoclusters was confirmed by EDS and EFTEM. Thus, the morphology of cast films consisted of SiO2 nanoclusters dispersed throughout the acrylate matrix. Strikingly, the untreated SiO2 nanoparticles induced significantly higher thermal decomposition temperatures, Td increased by as much as 20 degrees C relative to the neat acrylate. There was also an increase of glass transition temperature T-g and tensile modulus increased nearly 100% relative to the neat acrylate suggesting modification of macromolecular dynamics by the presence of the SiO2 nanoparticles, and this was confirmed by shear rheometry of the molten coatings where a rubber-like plateau was clearly defined. The results are contrasted for the same system but using batch polymerization. (C) 2016 Elsevier Ltd. All rights reserved.
机译:丙烯酸酯-SiO2纳米复合材料是通过使用未经处理的纳米粒子在水分散液中原位乳液半分批聚合合成的。在7 nm尺寸的SiO2纳米颗粒存在下,以50%的固含量共聚组成为56:42:2的丙烯酸丁酯(BA),甲基丙烯酸甲酯(MMA)和丙烯酸(AA)。 SiO 2纳米颗粒的添加量最高为3重量%,并且由此获得的乳液在室温下储存至少6个月是稳定的。半间歇聚合进行2.5小时。转化率高达92%且不低于84%,优于同一系统的间歇聚合。通过傅里叶变换红外光谱,热重分析,差示扫描量热,扫描和透射电子显微镜以及原子力显微镜对合成的乳液杂化物进行了表征。由于约1mm厚的流延膜是光学透明的,表明良好的纳米颗粒分散。然而,通过SEM,TEM和AFM检测到分散的SiO2纳米聚集体,并且通过EDS和EFTEM证实了纳米团簇的身份。因此,流延膜的形态由分散在整个丙烯酸酯基质中的SiO2纳米簇组成。令人惊讶的是,未经处理的SiO2纳米颗粒引起明显更高的热分解温度,相对于纯丙烯酸酯,Td升高了20摄氏度。相对于纯丙烯酸酯,玻璃化转变温度Tg也有所增加,拉伸模量增加了近100%,这表明存在SiO2纳米颗粒会改变大分子动力学,这可以通过熔融涂料的剪切流变法得到证实,其中橡胶-高原的定义很明确。对于同一系统但使用间歇聚合的结果进行了对比。 (C)2016 Elsevier Ltd.保留所有权利。

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