COMPONENT DYNAMICS IN MISCIBLE BLENDS OF 1,4-POLYISOPRENE AND 1,2-POLYBUTADIENE

被引:61
|
作者
ZAWADA, JA
FULLER, GG
COLBY, RH
FETTERS, LJ
ROOVERS, J
机构
[1] STANFORD UNIV,DEPT CHEM ENGN,STANFORD,CA 94305
[2] EASTMAN KODAK CO,IMAGING RES & ADV DEV,ROCHESTER,NY 14650
[3] EXXON RES & ENGN CO,CORP RES SCI LABS,ANNANDALE,NJ 08801
[4] NATL RES COUNCIL CANADA,INST ENVIRONM CHEM,OTTAWA K1A 0R6,ON,CANADA
关键词
D O I
10.1021/ma00101a026
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 effects of blending on the theology of the individual components in highly entangled miscible blends of 1,4-polyisoprene (PI) and 1,2-polybutadiene (1,2-PB) are investigated. Blend component contributions to the dynamic modulus, G*(omega), are recovered over the full composition range by complementing dynamic mechanical rheometry with infrared polarimetry. Distinct relaxations for each component are observed. Analysis of the modulus amplitudes of the component G*(omega) contributions reveals that the behavior of the slower relaxing component, 1,2-PB, compares well with constraint release scaling predictions. Each component is found to have a different average number of skeletal bonds between entanglements, in agreement with the predictions of an existing entanglement theory. The components appear to adopt a single reptation tube diameter and a mutual modulus shift factor, b(T)(T), in each blend. Analysis of the frequency dependence of the component G*(omega) contributions indicates that each component's relaxation is governed by a distinct apparent glass transition temperature, T-g, and that at a constant T - T-g blend composition only mildly influences the component relaxation times. A mild increase in the 1,2-PB relaxation time in the blend suggests a possible increase in the 1,2-PB friction factor in the presence of PI.
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页码:6861 / 6870
页数:10
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