Reactive spinning of cyanate aligned amino-functionalized ester fibers reinforced with single wall carbon nanotubes

被引:24
作者
Che, Jianfei [1 ,2 ]
Chan-Park, Mary B. [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637459, Singapore
[2] Nanjing Univ Sci & Technol, Mat Chem Lab, Nanjing 210094, Peoples R China
关键词
D O I
10.1002/adfm.200700919
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
We report a new approach of reactive spinning to fabricate thermosetting cyanate ester micro-scale diameter fibers with aligned single walled carbon nanotubes (SWNTs). The composite fibers were produced by first dispersing the SWNTs (1 wt%)in cyanate ester (CE) via solvent blending, followed by pre-polymerization, spinning and then multiple-stage curing. The pre-polymerization, spinning and post-spinning cure temperatures were carefully controlled to achieve good spun crosslinked fibers. Both pristine and amino-functionalized SWNTs were used for the reinforced fiber spinning. Amino-functionalized SWNTs (f-SWNTs) were prepared by reacting acid-treated SWNTs with toluene 2,4-diisocyanate and then ethylenediamine (EDA). FTIR, optical microscopy and scanning electron microscopy (SEM) showed that the amino-functionalized SWNTs were covalently and uniformly dispersed into the cyanate ester matrix and aligned along the fiber axis. The alignment was further confirmed using polarized Raman spectroscopy. The composite fibers with aligned amino-functionalized SWNTs possess improved tensile properties with respect to neat CE fibers, showing 85, 140, and 420% increase in tensile strength, elongation and stress-strain curve area (i.e., toughness), respectively. NH2-functionalization of SWNTs improves their dispersibility, alignment and interfacial strength and hence tensile properties of composite spun fibers. Fiber spinning to align SWNTs using thermosetting resin is novel. Others have reported fiber spinning to align SWNTs in thermoplastics. However, thermosetting CE resins offer the advantages of low and controllable viscosity during spinning and reactivity with amino functional groups to enable f-SWNT/CE covalent bonding.
引用
收藏
页码:888 / 897
页数:10
相关论文
共 48 条
[1]
Covalent surface chemistry of single-walled carbon nanotubes [J].
Banerjee, S ;
Hemraj-Benny, T ;
Wong, SS .
ADVANCED MATERIALS, 2005, 17 (01) :17-29
[2]
Fracture transitions at a carbon-nanotube/polymer interface [J].
Barber, AH ;
Cohen, SR ;
Eitan, A ;
Schadler, LS ;
Wagner, HD .
ADVANCED MATERIALS, 2006, 18 (01) :83-87
[3]
Carbon nanotubes - the route toward applications [J].
Baughman, RH ;
Zakhidov, AA ;
de Heer, WA .
SCIENCE, 2002, 297 (5582) :787-792
[4]
Big returns from small fibers: A review of polymer/carbon nanotube composites [J].
Breuer, O ;
Sundararaj, U .
POLYMER COMPOSITES, 2004, 25 (06) :630-645
[5]
Positron annihilation spectroscopy of polyacrylonitrile-based carbon fibers embedded with multi-wall carbon nanotubes [J].
Chakrabarti, K ;
Nambissan, PMG ;
Mukherjee, CD ;
Bardhan, KK ;
Kim, C ;
Yang, KS .
CARBON, 2006, 44 (05) :948-953
[6]
Mechanical reinforcement of polymers using carbon nanotubes [J].
Coleman, JN ;
Khan, U ;
Gun'ko, YK .
ADVANCED MATERIALS, 2006, 18 (06) :689-706
[7]
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
[8]
Super-tough carbon-nanotube fibres -: These extraordinary composite fibres can be woven into electronic textiles. [J].
Dalton, AB ;
Collins, S ;
Muñoz, E ;
Razal, JM ;
Ebron, VH ;
Ferraris, JP ;
Coleman, JN ;
Kim, BG ;
Baughman, RH .
NATURE, 2003, 423 (6941) :703-703
[9]
Mechanics of the interface for carbon nanotube-polymer composites [J].
Desai, AV ;
Haque, MA .
THIN-WALLED STRUCTURES, 2005, 43 (11) :1787-1803
[10]
LARGE-SCALE SYNTHESIS OF CARBON NANOTUBES [J].
EBBESEN, TW ;
AJAYAN, PM .
NATURE, 1992, 358 (6383) :220-222