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超支化聚酯改性对全同立构聚丙烯/氧化石墨烯复合材料结晶动力学的影响

Influences of Hyperbranched Polyester Modification on the Crystallization Kinetics of Isotactic Polypropylene/Graphene Oxide Composites.

作者信息

Hao Zengheng, Li Lu, Yang Bo, Sheng Xingyue, Liao Xia, He Leilei, Liu Pan

机构信息

Chongqing Zhixiang Paving Technology Engineering Co., Ltd., Chongqing 401336, China.

College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu 610065, China.

出版信息

Polymers (Basel). 2019 Mar 6;11(3):433. doi: 10.3390/polym11030433.

Abstract

In this study, the hyperbranched polyester grafted graphene oxide (GO-H202) was synthesized, and the isotactic polypropylene/graphene oxide (iPP/GO) composites were prepared. Results of X-ray photoelectron spectra (XPS), Fourier transform infrared (FT-IR), and transmission electron microscopy (TEM) revealed the successful synthesis of GO-H202, while thermogravimetric analysis (TGA) indicated that the weight ratio of grafting was about 35 wt %. Differential scanning calorimetry (DSC) and polarized optical microscopy (POM) were carried out to investigate the role of GO and GO-H202 on the crystallization kinetics of the composites. Results suggested that the addition of GO enhanced the nucleation rate and crystallizability of the composites, while GO-H202 exhibited a higher crystallization acceleration effect compared to neat GO; results of isothermal crystallization kinetics and self-nucleation isothermal crystallization kinetics showed that both the overall crystallization rate and crystal growth rate increase after the addition of GO and GO-H202, and the crystallization acceleration of GO-H202 became evidently stronger compared to GO. Moreover, the variation trends of Avrami exponent with the isothermal crystallization temperature changed significantly after the addition of GO or GO-H202, which might imply that the addition of GO and GO-H202 lead to different crystallization dimensionalities during the isothermal crystallization of the composites. The related mechanism was also discussed.

摘要

在本研究中,合成了超支化聚酯接枝氧化石墨烯(GO-H202),并制备了等规聚丙烯/氧化石墨烯(iPP/GO)复合材料。X射线光电子能谱(XPS)、傅里叶变换红外光谱(FT-IR)和透射电子显微镜(TEM)结果表明成功合成了GO-H202,而热重分析(TGA)表明接枝重量比约为35 wt%。进行差示扫描量热法(DSC)和偏光显微镜(POM)研究GO和GO-H202对复合材料结晶动力学的作用。结果表明,GO的加入提高了复合材料的成核速率和结晶能力,而GO-H202相比纯GO表现出更高的结晶加速效果;等温结晶动力学和自成核等温结晶动力学结果表明,加入GO和GO-H202后,整体结晶速率和晶体生长速率均增加,且GO-H202的结晶加速作用相比GO明显增强。此外,加入GO或GO-H202后,阿弗拉米指数随等温结晶温度的变化趋势发生显著变化,这可能意味着GO和GO-H202的加入导致复合材料等温结晶过程中出现不同的结晶维度。还讨论了相关机理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1c3/6473585/4ab0b526725b/polymers-11-00433-sch001.jpg

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