Morphological characteristics of solution spun nanocomposite fibers synthesized from ultra high molecular weight polyethylene, nylon-6 and carbon nanotubes, compatibilized with polyethylene-graft-maleic anhydride

被引:4
作者
Khan, Mujibur R. [1 ]
Absar, Saheem [1 ]
Mahfuz, Hassan [2 ]
Edwards, Kyle [3 ]
机构
[1] Georgia So Univ, Dept Mech Engn, Statesboro, GA 30460 USA
[2] Florida Atlantic Univ, Dept Ocean & Mech Engn, Boca Raton, FL 33431 USA
[3] Georgia So Univ, Dept Chem, Statesboro, GA 30460 USA
关键词
PHASE MORPHOLOGY; POLYMER BLENDS; CRYSTALLIZATION; POLYAMIDE; BEHAVIOR; REINFORCEMENT; POLYPROPYLENE; DISPERSION;
D O I
10.1134/S0965545X15060115
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Hybrid nanocomposite fibers from a blend of Ultrahigh molecular weight polyethylene (UHM-WPE)+Nylon-6+single-walled carbon nanotubes (SWCNT) were produced using a solution spinning process, both with and without a compatibilizer, Polyethylene-graft-Maleic Anhydride (PEG-g-MAH). The loading of Nylon-6, PE-g-MAH and SWCNTs was 20, 3, and 2 wt% of UHMWPE. A comparative morphological study of the fibers was performed using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR) analysis. SEM images of hybrid fiber cross-sections have shown polymer-coated SWCNTs aligned along the direction of extrusion inside the polymer. The blends with compatibilizer have shown rough and indistinct interfacial separation of the constituent phases, as seen in both cross-sectional and longitudinal views of fibers in SEM micrographs. Whereas, the samples without compatibilizer showed distinct minor polymer phase as droplets. DSC results indicate reduction of crystallinity, crystallization rate and lamellar size in the compatibilized blends. Comparative FTIR analysis of the fiber blends showed the presence of new absorbance peaks (at 1753.62 and 1210-990 cm(-1)) suggesting formation of imide linkages between the UHMWPE backbone and Nylon-6 chains in the blends with compatibilizer via reactive functional groups present in the PE-g-MAH. The appearance of these peaks were more prominent when nanotubes were present in the blend.
引用
收藏
页码:863 / 873
页数:11
相关论文
共 46 条
[11]  
Hannay N. B., 1977, TREATISE SOLID STATE
[12]   PARTICLE DIMENSIONS IN POLYSTYRENE-POLYETHYLENE BLENDS AS A FUNCTION OF THEIR MELT VISCOSITY AND OF CONCENTRATION OF ADDED GRAFT COPOLYMER [J].
HEIKENS, D ;
BARENTSEN, W .
POLYMER, 1977, 18 (01) :69-72
[13]   STUDIES ON POLYMER BLEND OF NYLON-6 AND POLYPROPYLENE OR NYLON-6 AND POLYSTYRENE USING REACTION OF POLYMER [J].
IDE, F ;
HASEGAWA, A .
JOURNAL OF APPLIED POLYMER SCIENCE, 1974, 18 (04) :963-974
[14]   Study on poly(methyl methacrylate)/carbon nanotube composites [J].
Jia, ZJ ;
Wang, ZY ;
Xu, CL ;
Liang, J ;
Wei, BQ ;
Wu, DH ;
Zhu, SW .
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING, 1999, 271 (1-2) :395-400
[15]   Reactive compatibilizer precursors for LDPE/PA6 blends. II: maleic anhydride grafted polyethylenes [J].
Jiang, CH ;
Filippi, S ;
Magagnini, P .
POLYMER, 2003, 44 (08) :2411-2422
[16]   A Study of Mechanical Behavior and Morphology of Carbon Nanotube Reinforced UHMWPE/Nylon 6 Hybrid Polymer Nanocomposite Fiber [J].
Khan, Mujibur R. ;
Mahfuz, Hassan ;
Adnan, Ashfaq ;
Leventouri, Theodora ;
Absar, Saheem .
FIBERS AND POLYMERS, 2014, 15 (07) :1484-1492
[17]   Effect of strain hardening on the elastic properties and normalized velocity of hybrid UHMWPE-nylon 6-SWCNT nanocomposites fiber [J].
Khan, Mujibur R. ;
Mahfuz, Hassan ;
Leventouri, Theodora .
JOURNAL OF MATERIALS RESEARCH, 2012, 27 (20) :2657-2667
[18]  
Larkin PJ, 2011, INFRARED AND RAMAN SPECTROSCOPY: PRINCIPLES AND SPECTRAL INTERPRETATION, P1
[19]   Nanohybrid Shish-kebabs: Periodically functionalized carbon nanotubes [J].
Li, CY ;
Li, LY ;
Cai, WW ;
Kodjie, SL ;
Tenneti, KK .
ADVANCED MATERIALS, 2005, 17 (09) :1198-+
[20]  
Li ZM, 2007, POLYM-PLAST TECHNOL, V46, P129, DOI [10.1080/03602550601152929, 10.1080/036025506011152929]