Rheological properties of diblock copolymer/layered silicate nanocomposites

被引:71
作者
Mitchell, CA [1 ]
Krishnamoorti, R [1 ]
机构
[1] Univ Houston, Dept Chem Engn, Houston, TX 77204 USA
关键词
block copolymers; nanocomposites; rheology;
D O I
10.1002/polb.10209
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 melt-state viscoelastic properties of nanocomposites prepared with a symmetrical polystyrene-polyisoprene block copolymer and organically modified layered silicates are examined. Nanocomposites based on three thermodynamically equivalent organically modified layered silicates, primarily differing in lateral disk diameter (d), are studied with small-amplitude oscillatory shear. The effects of the domain structure of the ordered block copolymer and the mesoscale dispersion of the layered silicates on the rheological properties are examined via a comparison of data for the nanocomposites in the ordered and disordered states of the block copolymer. Hybrids prepared with 5 wt % organically modified fluorohectorite (d similar to 10 mum) and montmorillonite (d similar to 1 mum) demonstrate a notable decrease in the frequency dependence of the moduli at low frequencies and a significant enhancement in the complex viscosity at low frequencies in the disordered state. This behavior is understood in terms of the development of a percolated layered-silicate network structure. However, the viscoelastic properties in the disordered state with 5 wt % organically modified laponite (d similar to 30 nm) and in the ordered state of the block copolymer for all layered silicates demonstrate only minor changes from those observed for the unfilled polymer. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:1434 / 1443
页数:10
相关论文
共 40 条
[1]   RHEOLOGY AND THE MICROPHASE SEPARATION TRANSITION IN STYRENE-ISOPRENE BLOCK-COPOLYMERS [J].
ADAMS, JL ;
GRAESSLEY, WW ;
REGISTER, RA .
MACROMOLECULES, 1994, 27 (21) :6026-6032
[2]   Multi-scale model for binary mixtures containing nanoscopic particles [J].
Balazs, AC ;
Ginzburg, VV ;
Qiu, F ;
Peng, GW ;
Jasnow, D .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (15) :3411-3422
[3]   Modeling the phase behavior of polymer/clay nanocomposites [J].
Balazs, AC ;
Singh, C ;
Zhulina, E ;
Lyatskaya, Y .
ACCOUNTS OF CHEMICAL RESEARCH, 1999, 32 (08) :651-657
[4]   Modeling the interactions between polymers and clay surfaces through self-consistent field theory [J].
Balazs, AC ;
Singh, C ;
Zhulina, E .
MACROMOLECULES, 1998, 31 (23) :8370-8381
[5]   Identification of the molecular parameters that govern ordering kinetics in a block copolymer melt [J].
Balsara, NP ;
Garetz, BA ;
Chang, MY ;
Dal, HJ ;
Newstein, MC .
MACROMOLECULES, 1998, 31 (16) :5309-5315
[6]   FLUCTUATION EFFECTS IN A SYMMETRIC DIBLOCK COPOLYMER NEAR THE ORDER-DISORDER TRANSITION [J].
BATES, FS ;
ROSEDALE, JH ;
FREDRICKSON, GH .
JOURNAL OF CHEMICAL PHYSICS, 1990, 92 (10) :6255-6270
[7]  
Ferry D.J., 1980, Viscoelastic Properties of Polymers, V3e
[8]   Packing length influence in linear polymer melts on the entanglement, critical, and reptation molecular weights [J].
Fetters, LJ ;
Lohse, DJ ;
Milner, ST ;
Graessley, WW .
MACROMOLECULES, 1999, 32 (20) :6847-6851
[9]   Nylon 6 nanocomposites: the effect of matrix molecular weight [J].
Fornes, TD ;
Yoon, PJ ;
Keskkula, H ;
Paul, DR .
POLYMER, 2001, 42 (25) :9929-9940
[10]   Dynamics of block copolymers: Theory and experiment [J].
Fredrickson, GH ;
Bates, FS .
ANNUAL REVIEW OF MATERIALS SCIENCE, 1996, 26 :501-550