KINETICS OF CRAZING IN POLYBUTADIENE POLYSTYRENE BLENDS

被引:8
|
作者
SPIEGELBERG, SH
ARGON, AS
COHEN, RE
机构
[1] MIT,DEPT CHEM ENGN,CAMBRIDGE,MA 02139
[2] MIT,DEPT MECH ENGN,CAMBRIDGE,MA 02139
关键词
D O I
10.1002/app.1994.070530912
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 crazing behavior of blends of polystyrene (PS) and a low molecular weight polybutadiene (PB)was examined as part of a continuing study of toughening mechanisms in thermoplastic polymers. These PS/PB blends attain high levels of toughness from the stress-activated plasticizing action of the polybutadiene (PB), a mechanism that is active only in the region of a growing craze. The plasticization is therefore localized and leads to enhanced toughness without loss in stiffness. The net result of this plasticization is a reduction in craze flow stress accompanied by an increase in craze velocity, which, in turn, allows the specimen to reach substantial strains-to-fracture in uniaxial deformation under an imposed strain rate. The ability of the PB to plasticize a growing craze is expected to be a function of the mobility of the PB. To investigate the role of diluent mobility, tensile tests and craze velocity measurements were conducted at -20-degrees-C and compared with previously published results collected at 23-degrees-C. Although the blends displayed high levels of toughness at 23-degrees-C, the blends tested at -20-degrees-C showed brittle behavior. Craze velocities measured at -20-degrees-C were 2 orders of magnitude lower than the results at 23-degrees-C. Addition of 3 wt % PB at -20-degrees-C led to craze velocities only as large as those found in pure PS at 23-degrees-C. Comparison of the craze velocities with an asymptotic theoretical model describing the dependence of the craze velocity on the PB content showed good agreement with the results at -20-degrees-C and only fair agreement with the room-temperature results. (C) 1994 John Wiley & Sons, Inc.
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页码:1251 / 1259
页数:9
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