Functionalized carbon nanotube/polyacrylonitrile composite nanofibers: fabrication and properties

被引:18
作者
Wang, Kaitao [1 ]
Gu, Mingbo [1 ]
Wang, Jian-jun [1 ]
Qin, Chuanxiang [1 ]
Dai, Lixing [1 ]
机构
[1] Soochow Univ, Coll Chem, Chem Engn & Mat Sci, Suzhou 215123, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
polyacrylonitrile; multi-walled carbon nanotubes; friedel-crafts acylation; electrospinning; MECHANICAL-PROPERTIES; NANOTUBE; FIBERS; DISPERSION; POLYMERIZATION; NANOCOMPOSITES; OXIDATION;
D O I
10.1002/pat.1866
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The functionalized multi-walled carbon nanotubes (f-MWCNTs) were obtained by FriedelCrafts acylation, which introduced aromatic amine groups onto the sidewall. And the grafted yield was adjusted by controlling the concentration of the catalyst. The composite solutions containing f-MWCNTs and polyacrylonitrile (PAN) were then prepared by in-situ or ex-situ solution polymerization. The resulting solutions were electrospun into composite nanofibers. In the in-situ polymerization, morphological observation revealed that f-MWCNTs was uniformly dispersed along the axes of the nanofibers and increased interfacial adhesion between f-MWCNTs and PAN. Furthermore, two kinds of f-MWCNTs/PAN composite nanofibers had a higher degree of crystallization and a larger crystal size than PAN nanofibers had, so the specific tensile strengths and modulus of the composite nanofibers were enhanced. And the thermal stability of f-MWCNTs/PAN from in-situ method was higher than that of ex-situ system. When the f-MWCNTs content was less than 1wt%, the specific tensile strengths and modulus of nanofibers were enhanced with increase in the amounts of f-MWCNTs, and f-MWCNTs/PAN of in-situ system provided better mechanical properties than that of ex-situ system. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:262 / 271
页数:10
相关论文
共 44 条
[1]  
[Anonymous], 2000, Structure Determination of organic compounds
[2]   Covalent modification of vapour-grown carbon nanofibers via direct Friedel-Crafts acylation in polyphosphoric acid [J].
Baek, JB ;
Lyons, CB ;
Tan, LS .
JOURNAL OF MATERIALS CHEMISTRY, 2004, 14 (13) :2052-2056
[3]   THERMOREVERSIBLE GELATION AND PLASTICIZATION OF POLYACRYLONITRILE [J].
BASHIR, Z .
POLYMER, 1992, 33 (20) :4304-4313
[4]   Carbon nanotubes - the route toward applications [J].
Baughman, RH ;
Zakhidov, AA ;
de Heer, WA .
SCIENCE, 2002, 297 (5582) :787-792
[5]   CHANGES IN STRUCTURE OF WET-SPUN ACRYLIC FIBERS DURING PROCESSING [J].
BELL, JP ;
DUMBLETO, JH .
TEXTILE RESEARCH JOURNAL, 1971, 41 (03) :196-+
[6]   Big returns from small fibers: A review of polymer/carbon nanotube composites [J].
Breuer, O ;
Sundararaj, U .
POLYMER COMPOSITES, 2004, 25 (06) :630-645
[7]   Processing and microstructural characterization of porous biocompatible protein polymer thin films [J].
Buchko, CJ ;
Chen, LC ;
Shen, Y ;
Martin, DC .
POLYMER, 1999, 40 (26) :7397-7407
[8]   Multiwalled carbon nanotubes grafted with polyhedral oligomeric silsesquioxane and its dispersion in poly(L-lactide) matrix [J].
Chen, Guang-Xin ;
Shimizu, Hiroshi .
POLYMER, 2008, 49 (04) :943-951
[9]   An assessment of the science and technology of carbon nanotube-based fibers and composites [J].
Chou, Tsu-Wei ;
Gao, Limin ;
Thostenson, Erik T. ;
Zhang, Zuoguang ;
Byun, Joon-Hyung .
COMPOSITES SCIENCE AND TECHNOLOGY, 2010, 70 (01) :1-19
[10]   Small but strong: A review of the mechanical properties of carbon nanotube-polymer composites [J].
Coleman, Jonathan N. ;
Khan, Umar ;
Blau, Werner J. ;
Gun'ko, Yurii K. .
CARBON, 2006, 44 (09) :1624-1652