首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >Nylon 610/functionalized multiwalled carbon nanotube composite prepared from in-situ interfacial polymerization
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Nylon 610/functionalized multiwalled carbon nanotube composite prepared from in-situ interfacial polymerization

机译:原位界面聚合制备尼龙610 /功能化多壁碳纳米管复合材料

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摘要

Pristine multiwalled carbon nanotubes (P-MWNTs) were functionalized. with 4-chlorobenzoic acid via "direct" Friedel-Crafts acylation in polyphosphoric acid (PPA)/phosphorous pentoxide (P2O5) medium. The resultant 4-chlorobenzoyl-functionalized MWNTs (F-MWNTs) were soluble in chlorinated solvents such as dichloromethane, chloroform, and carbon tetrachloride. A large scale of nylon 610/F-MWNT composite could be conveniently prepared by in situ interfacial polymerization of 1, 6-hexamethylenediamine (HMDA) in an aqueous phase, and sebacoyl chloride with F-MWNTs in an organic phase. Similarly, nylon 610/P-MWNT composite was also prepared for comparison. The state of F-MWNTs dispersion in nylon 610 matrix was distinctively better than that of P-MWNTs, which could be clearly discerned by both naked eye and scanning electron microcopy (SEM). As a result, the tensile strength of nylon 610/F-MWNT composite was 4.9-fold higher than that of nylon 610/P-MWNT composite. (C) 2008 Wiley Periodicals, Inc.
机译:原始的多壁碳纳米管(P-MWNTs)进行了功能化。在多磷酸(PPA)/五氧化二磷(P2O5)介质中通过“直接” Friedel-Crafts酰化反应与4-氯苯甲酸反应。所得的4-氯苯甲酰基官能化的MWNT(F-MWNT)可溶于氯化溶剂,例如二氯甲烷,氯仿和四氯化碳。通过在水相中进行1,6-己二胺(HMDA)和癸二酰氯与有机相中的F-MWNT的原位界面聚合,可以方便地制备大规模的尼龙610 / F-MWNT复合材料。同样,还准备了尼龙610 / P-MWNT复合材料进行比较。 F-MWNTs在尼龙610基质中的分散状态明显优于P-MWNTs,这可以通过肉眼和扫描电子显微镜(SEM)清楚地看出。结果,尼龙610 / F-MWNT复合材料的拉伸强度比尼龙610 / P-MWNT复合材料的拉伸强度高4.9倍。 (C)2008 Wiley期刊公司

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