COMPOSITION DEPENDENCE OF THE VISCOELASTICITY OF END-LINKED POLY(DIMETHYLSILOXANE) AT THE GEL POINT

被引:323
作者
SCANLAN, JC [1 ]
WINTER, HH [1 ]
机构
[1] UNIV MASSACHUSETTS,DEPT CHEM ENGN,AMHERST,MA 01003
关键词
D O I
10.1021/ma00001a008
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Precursor composition is shown to have a considerable impact on the viscoelastic properties of a polymer at the gel point. End-linked poly(dimethylsiloxane) polymers were prepared with various stoichiometry, chain length, and concentration. The power law relaxation modulus, G(t) = St(-n), identifies the gel point, and a small frequency window (2 decades) is sufficient to determine the relaxation exponent, n, and gel strength, S. Both are shown to be strongly composition dependent. The relaxation exponent ranges between 0.19 and 0.92 in this study, which is almost the entire possible range (0 < n < 1). The gel strength ranges over 5 decades. A prepolymer below the entanglement molecular weight produces critical gels with relaxation exponents in the range 0.4-0.7, depending on stoichiometry. A high molecular weight prepolymer, above the entanglement molecular weight, produces critical gels with lower n values, in the range of 0.2-0.4, depending on stoichiometry. Addition of a diluent also affects the relaxation exponent, and near the overlap concentration n approaches the limit of 1. In a series of experiments with different stoichiometry and concentration, S and n appear to be related by a material characteristic function S = G0-lambda-0n, where G0 and lambda-0 are characteristic constants of the precursor material and n depends on composition.
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页码:47 / 54
页数:8
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