Effective interaction parameter between branched and linear polystyrene

被引:35
作者
Greenberg, CC
Foster, MD [1 ]
Turner, CM
Corona-Galvan, S
Cloutet, E
Quirk, RP
Butler, PD
Hawker, C
机构
[1] Univ Akron, Maurice Morton Inst Polymer Sci, Akron, OH 44325 USA
[2] Natl Inst Stand & Technol, Ctr Neutron Res, Gaithersburg, MD 20899 USA
[3] IBM Corp, Almaden Res Ctr, San Jose, CA 95120 USA
关键词
star polymers; long-chain branching; phase behavior; small-angle neutron scattering (SANS); thermodynamics;
D O I
10.1002/polb.10017
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Values of the effective interaction parameter (X) between regular, long-branched polystyrene chains and their linear analogues were measured with small-angle neutron scattering for several star-branched chains and one comb-type polymer. The contribution to this interaction due to architecture alone increases monotonically with star functionality for the set of polymers studied here. The interaction appears to be less sensitive to variations in arm size than would be expected from fluctuation theory predictions by G. H. Fredrickson, A. Liu, and F. S. Bates (Macromolecules 1994, 27, 2503) for a purely entropic interaction due to architecture. The change in chi with the volume fraction of the star in the blend is in agreement with the theory, however. The magnitudes of the interaction in the star/linear blends are small enough that bulk phase separation is unlikely, whereas that in the comb/linear blend is about 20 times higher for the same number of arms. Thus, bulk phase separation can be readily expected for comb/linear blends at commercially relevant values of molecular weights. (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:2549 / 2561
页数:13
相关论文
共 38 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]   Small angle neutron scattering investigations of melt miscibility and phase segregation in blends of linear and branched polyethylenes as a function of the branch content [J].
Alamo, RG ;
Graessley, WW ;
Krishnamoorti, R ;
Lohse, DJ ;
Londono, JD ;
Mandelkern, L ;
Stehling, FC ;
Wignall, GD .
MACROMOLECULES, 1997, 30 (03) :561-566
[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]   SMALL-ANGLE NEUTRON-SCATTERING BY PARTIALLY DEUTERATED POLYMERS AND THEIR BLENDS [J].
BALSARA, NP ;
LOHSE, DJ ;
GRAESSLEY, WW ;
KRISHNAMOORTI, R .
JOURNAL OF CHEMICAL PHYSICS, 1994, 100 (05) :3905-3910
[5]   ISOTOPE-INDUCED QUANTUM-PHASE TRANSITIONS IN THE LIQUID-STATE [J].
BATES, FS ;
WIGNALL, GD .
PHYSICAL REVIEW LETTERS, 1986, 57 (12) :1429-1432
[6]   TACTICITY EFFECTS ON POLYMER BLEND MISCIBILITY [J].
BEAUCAGE, G ;
STEIN, RS ;
HASHIMOTO, T ;
HASEGAWA, H .
MACROMOLECULES, 1991, 24 (11) :3443-3448
[7]   TEMPERATURE COEFFICIENTS FOR THE CHAIN DIMENSIONS OF POLYSTYRENE ANDPOLYMETHYLMETHACRYLATE [J].
BOOTHROYD, AT ;
RENNIE, AR ;
WIGNALL, GD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 99 (11) :9135-9144
[8]  
Chen YY, 2000, J POLYM SCI POL PHYS, V38, P2965, DOI 10.1002/1099-0488(20001115)38:22<2965::AID-POLB120>3.0.CO
[9]  
2-A
[10]   PHASE-BEHAVIOR OF LINEAR BRANCHED POLYMER BLENDS [J].
CLARKE, N ;
MCLEISH, TCB ;
JENKINS, SD .
MACROMOLECULES, 1995, 28 (13) :4650-4659