The effect of interfacial chemistry on molecular mobility and morphology of multiwalled carbon nanotubes epoxy nanocomposite

被引:222
作者
Abdalla, Mohamed
Dean, Derrick
Adibempe, David
Nyairo, Elijah
Robinson, Pamela
Thompson, Gregory
机构
[1] Univ Alabama Birmingham, Dept Mat Sci & Engn, Birmingham, AL 35294 USA
[2] Think Tank Innovat, Baltimore, MD USA
[3] Alabama State Univ, Dept Phys Sci, Montgomery, AL 36101 USA
[4] Tuskegee Univ, Dept Chem, Tuskegee, AL 36088 USA
[5] Univ Alabama, Dept Met & Mat Engn, Tuscaloosa, AL 35487 USA
关键词
carbon nanotubes; epoxy nanocomposite; rheology;
D O I
10.1016/j.polymer.2007.06.073
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report on our attempts to understand the link between the nature of the CNT surface modification, dispersion in an epoxy resin and the resulting properties. Carboxylated and fluorinated nanotubes were used to synthesize nanocomposites by dispersing them separately in an epoxy resin. Dynamic mechanical analysis, using torsional deformation, was applied both parallel and perpendicular to the long axis of the multiwall nanotubes (MWNTs). Interestingly, for epoxy/MWNT (1 wt%) nanocomposites, the shear moduli in the glassy state were higher for the nanocomposites, and it's highest for the nanocomposites in which the nanotubes are parallel to the direction of applied torque. These nanocomposites also exhibited higher T(g)s than the neat resin. In addition, the rubbery plateau modulus (between 150-200 degrees C) was higher by a factor of three for the nanocomposites. Master curves constructed using time-temperature superposition allowed us to probe low frequency dynamic moduli and further discern differences in the relaxation behavior. Samples containing fluorinated nanotubes exhibited the highest TgS, longest relaxation times and highest activation energies relative to the carboxylated nanotube samples and the neat resin, indicative of stronger interactions. SEM and TEM studies confirmed the nanotube dispersion and alignment. (C) 2007 Elsevier Ltd. All rights reserved.
引用
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页码:5662 / 5670
页数:9
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