新型哑铃状苯基倍半硅氧烷增强的聚苯乙烯纳米复合材料:合成与热性能表征

Polystyrene Nanocomposites Reinforced with Novel Dumbbell-Shaped Phenyl-POSSs: Synthesis and Thermal Characterization.

作者信息

Abate Lorenzo, Bottino Francesco Agatino, Cicala Gianluca, Chiacchio Maria Assunta, Ognibene Giulia, Blanco Ignazio

机构信息

Department of Civil Engineering and Architecture and INSTM UdR, University of Catania, V.le A. Doria 6, 95125 Catania, Italy.

Department of Chemical Science, University of Catania, V.le A. Doria 6, 95125 Catania, Italy.

出版信息

Polymers (Basel). 2019 Sep 9;11(9):1475. doi: 10.3390/polym11091475.

Abstract

Two series of novel dumbbell-shaped polyhedral oligomeric silsesquioxanes (POSSs), fully functionalized with phenyl groups at the corner of the silicon cages, were used to prepare polystyrene (PS) nanocomposites through the method of in situ polymerization. The percentage of the molecular filler reinforcement was set as 5% / of POSS and was checked by H-NMR spectroscopy. The obtained nanocomposites were characterized by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). Thermal and morphological properties were evaluated and compared among the nanocomposites obtained using the two different series of dumbbell-shaped POSSs and with the net PS. The thermal parameters for the prepared nanocomposites were very high when compared with those of neat PS, and they evidenced significant differences when an aliphatic or aromatic bridge was used to link the silicon cages. SEM analysis results allow us to hypothesize a justification for the different resistance to thermal degradation showed by the two series of molecular reinforcement.

摘要

制备了两个系列的新型哑铃状多面体低聚倍半硅氧烷(POSS),它们在硅笼的角上被苯基完全官能化,通过原位聚合法用于制备聚苯乙烯(PS)纳米复合材料。分子填充增强剂的百分比设定为5%的POSS,并通过H-NMR光谱进行检测。通过热重分析(TGA)、差示扫描量热法(DSC)、傅里叶变换红外光谱(FTIR)和扫描电子显微镜(SEM)对所得纳米复合材料进行了表征。对使用两种不同系列哑铃状POSS获得的纳米复合材料以及纯PS的热性能和形态性能进行了评估和比较。与纯PS相比,制备的纳米复合材料的热参数非常高,并且当使用脂肪族或芳香族桥连接硅笼时,它们表现出显著差异。SEM分析结果使我们能够推测出两种系列分子增强剂对热降解具有不同抗性的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6147/6780803/8065f8ade505/polymers-11-01475-g001.jpg

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