New insights into reinforcement mechanism of nanoclay-filled isoprene rubber during uniaxial deformation by in situ synchrotron X-ray diffraction

被引:39
作者
Fu, Xuan [1 ]
Huang, Guangsu [1 ]
Xie, Zhengtian [1 ]
Xing, Wang [1 ]
机构
[1] Sichuan Univ, Coll Polymer Sci & Engn, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
STRAIN-INDUCED CRYSTALLIZATION; STRESS-INDUCED CRYSTALLIZATION; CROSSLINKED NATURAL-RUBBER; ANGLE NEUTRON-SCATTERING; ALPHA-TERMINAL GROUP; STRUCTURAL DEVELOPMENT; MOLECULAR-ORIENTATION; SYNTHETIC RUBBERS; BRANCH-POINTS; TUBE MODEL;
D O I
10.1039/c5ra02123e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The strain-induced crystallization (SIC) behavior of unfilled and organically modified montmorillonite (OMMT)-filled cis-1,4-polyisoprene rubber (IR) were analyzed by using synchrotron wide-angle X-ray diffraction (WAXD). The inclusion of highly anisotropic nanoclay reinforces the rubber matrix by introducing a mass of physical crosslinking points (entanglements). An early promotion of SIC was observed in the nanocomposites during uniaxial stretching, as well as enhancement of overall crystallization. The reinforcement of IR and the enhancement of SIC both show strong OMMT concentration dependence and most manifest at a filler loading of 5 wt%, at which content the OMMT reaches a saturated dispersion. The adsorption of rubber chains on the surface of OMMT will form a 'denser network domain' due to the strong filler-rubber interaction. During the deformation, the crystallites emerge from the highly stretched short chains in the "denser network domain" and strengthen the whole network. The large effective specific surface and aspect ratios of OMMT play a vital role in interpreting the reinforcement of nanoclay-filled IR.
引用
收藏
页码:25171 / 25182
页数:12
相关论文
共 72 条
[11]   Miscibility-dispersion, interfacial strength and nanoclay mobility relationships in polymer nanocomposites [J].
Carretero-Gonzalez, Javier ;
Retsos, Haris ;
Giannelis, Emmanuel P. ;
Ezquerra, Tiberio A. ;
Hernandez, Marianella ;
Lopez-Manchado, Miguel A. .
SOFT MATTER, 2009, 5 (18) :3481-3486
[12]   Parameters governing strain induced crystallization in filled natural rubber [J].
Chenal, Jean-Marc ;
Gauthier, Catherine ;
Chazeau, Laurent ;
Guy, Laurent ;
Bomal, Yves .
POLYMER, 2007, 48 (23) :6893-6901
[13]   Molecular weight between physical entanglements in natural rubber: A critical parameter during strain-induced crystallization [J].
Chenal, Jean-Marc ;
Chazeau, Laurent ;
Guy, Laurent ;
Bomal, Yves ;
Gauthier, Catherine .
POLYMER, 2007, 48 (04) :1042-1046
[14]   Strain-crystallization of guayule and hevea rubbers [J].
Choi, IS ;
Roland, CM .
RUBBER CHEMISTRY AND TECHNOLOGY, 1997, 70 (02) :202-210
[15]   THE INFLUENCE OF FINITE EXTENSIBILITY OF THE CHAINS ON THE ORIENTATION BEHAVIOR OF A POLYMER NETWORK [J].
DIETRICH, J ;
ORTMANN, R ;
BONART, R .
COLLOID AND POLYMER SCIENCE, 1988, 266 (04) :299-310
[16]  
Flory P.J., 1953, Principles of polymer chemistry, P266
[18]   DYNAMIC TESTING AND REINFORCEMENT OF RUBBER [J].
FUNT, JM .
RUBBER CHEMISTRY AND TECHNOLOGY, 1988, 61 (05) :842-865
[19]   Observations on the X-ray structure of rubber and the size and shape of rubber crystallites [J].
Gehman, SD ;
Field, JE .
JOURNAL OF APPLIED PHYSICS, 1944, 15 (04) :371-379
[20]   An X-ray investigation of crystallinity in rubber [J].
Gehman, SD ;
Field, JE .
JOURNAL OF APPLIED PHYSICS, 1939, 10 (08) :564-572