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首页> 外文期刊>Polymers for advanced technologies >Poly(butylene terephthalate)-functionalized MWNTs by in situ ring-opening polymerization of cyclic butylene terephthalate oligomers
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Poly(butylene terephthalate)-functionalized MWNTs by in situ ring-opening polymerization of cyclic butylene terephthalate oligomers

机译:原位开环聚合对苯二甲酸丁二醇酯低聚物的聚对苯二甲酸丁二酯官能化的多壁碳纳米管

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摘要

Poly(butylene terephthalate) (PBT) had been covalently attached onto the surface of multiwalled carbon nanotubes (MWNTs) by a "grafting from" method based on in situ ring-opening polymerization (ROP) of cyclic butylene terephthalate oligomers (CBT) using MWNT-supported initiator (MWNT-g-Sn). The Sn-O bond grafted on the surface of MWNTs, which was confirmed by X-ray photoelectron spectroscopy, provided the initiating sites for ROP of CBT. Fourier transformed infrared spectroscopy and nuclear magnetic resonance were used to confirm the chemical structure of MWNT-graft-PBT copolymer and emission transmission electron microscope was utilized to observe the nanostructure of the PBT functionalized MWNTs. A distinct core-shell structure with PBT layer as the shell could be observed after functionalization of PBT despite it was not uniform. The results of thermogravimetric analysis indicated that the grafting ratio of PBT was about 59.3%. Furthermore, the solubility of the PBT functionalized MWNTs in phenol/tetrachloroethane had also been investigated.
机译:聚对苯二甲酸丁二酯(PBT)已通过“接枝”方法共价连接到多壁碳纳米管(MWNT)的表面上,该方法基于使用MWNT的环对苯二甲酸丁二酯低聚物(CBT)的原位开环聚合(ROP)支持的启动器(MWNT-g-Sn)。 X射线光电子能谱证实了嫁接在MWNT表面的Sn-O键为CBT的ROP提供了起始位置。利用傅里叶变换红外光谱和核磁共振技术确定了MWNT-接枝-PBT共聚物的化学结构,并用发射透射电镜观察了PBT官能化MWNTs的纳米结构。尽管PBT功能不均匀,但在PBT官能化后仍可观察到以PBT层为壳的独特核-壳结构。热重分析结果表明,PBT的接枝率约为59.3%。此外,还研究了PBT官能化的MWNT在苯酚/四氯乙烷中的溶解度。

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