Phase behavior of partially miscible ethylene-styrene copolymer blends

被引:12
作者
Chen, HY
Chum, SP
Hiltner, A [1 ]
Baer, E
机构
[1] Case Western Reserve Univ, Dept Macromol Sci, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, CAPRI, Cleveland, OH 44106 USA
[3] Dow Chem Co USA, Polyolefins & Elastomers R&D, Freeport, TX 77541 USA
关键词
D O I
10.1021/ma002143b
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Blends of ethylene-styrene copolymers were studied as a model system for miscibility of alpha -olefin copolymer blends. The phase behavior of partially miscible copolymers, with styrene content difference; of 9-10 wt %, was characterized by phase diagrams. Blends were rapidly quenched from the melt to retain the phase morphology, and the volume fractions of the two phases were obtained from AFM. phase images. Assuming monodisperse polymers, the phase composition was approximated by extrapolation of the relationship between blend composition and phase volume fraction. The blends exhibited an upper critical solution temperature (UCST). With decreasing molecular weight and decreasing styrene content difference, the blends became more miscible and the UCST decreased. However, the chi interaction parameter extracted from the phase compositions varied with molecular weight, contrary to expectations, and did not show the expected squared dependence on styrene content difference. Much better results were obtained with an approach that considered the molecular weight distribution. Although the polydispersity of ethylene-styrene copolymers is relatively small, the analysis indicated that phase composition depended on initial blend composition The chi parameter obtained with this approach was independent of molecular weight and was proportional to the square of the styrene content difference. The solubility parameter difference extracted from the chi parameter agreed with literature values.
引用
收藏
页码:4033 / 4042
页数:10
相关论文
共 31 条
[1]   PHASE-BEHAVIOR OF BLENDS OF LINEAR AND BRANCHED POLYETHYLENES IN THE MOLTEN AND SOLID STATES BY SMALL-ANGLE NEUTRON-SCATTERING [J].
ALAMO, RG ;
LONDONO, JD ;
MANDELKERN, L ;
STEHLING, FC ;
WIGNALL, GD .
MACROMOLECULES, 1994, 27 (02) :411-417
[2]  
[Anonymous], [No title captured]
[3]   THERMODYNAMIC INTERACTIONS IN MODEL POLYOLEFIN BLENDS OBTAINED BY SMALL-ANGLE NEUTRON-SCATTERING [J].
BALSARA, NP ;
FETTERS, LJ ;
HADJICHRISTIDIS, N ;
LOHSE, DJ ;
HAN, CC ;
GRAESSLEY, WW ;
KRISHNAMOORTI, R .
MACROMOLECULES, 1992, 25 (23) :6137-6147
[4]  
Chen H, 1998, J APPL POLYM SCI, V70, P109, DOI 10.1002/(SICI)1097-4628(19981003)70:1<109::AID-APP11>3.0.CO
[5]  
2-2
[6]  
Chen HY, 1999, J POLYM SCI POL PHYS, V37, P2373, DOI 10.1002/(SICI)1099-0488(19990901)37:17<2373::AID-POLB8>3.0.CO
[7]  
2-M
[8]   Large strain stress relaxation and recovery behavior of amorphous ethylene-styrene interpolymers [J].
Chen, HY ;
Stepanov, EV ;
Chum, SP ;
Hiltner, A ;
Baer, E .
MACROMOLECULES, 1999, 32 (22) :7587-7593
[9]   Linear stress relaxation behavior of amorphous ethylene-styrene interpolymers [J].
Chen, HY ;
Stepanov, EV ;
Chum, SP ;
Hiltner, A ;
Baer, E .
MACROMOLECULES, 2000, 33 (23) :8870-8877
[10]  
CHEN HY, IN PRESS POLYMER