Evolution of phase dimensions and interfacial morphology of polypropylene/polystyrene compatibilized blends during mixing

被引:30
|
作者
Li, Yun-yan
hu, Sang-wei Hu
Sheng, Jing [1 ]
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
[2] Nankai Univ, Math Inst, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
phase morphology; polystyrene; polypropylene; fractal;
D O I
10.1016/j.eurpolymj.2006.10.018
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 morphology development of polypropylene/polystyrene (PP/PS) blends was studied by means of effective mathematics methods. Time resolved fracture morphology measurements on PP/PS (20/80) blends compatibilized with styrenebutadiene-styrene block copolymer (SBS) suggested that PP/SBS domains acted as a warehouse supplying compatibilizer (SBS) to the phase boundary in the initial stage of mixing and promoted the formation and development of the transition layer. The development of the transition layer leaded to a more complicated morphology of fracture surface and strengthened the adhesion between phases, which was quantitatively investigated using Brown fractal dimension D-Brown. In the early stage of the mixing (< 2.0 min), the mean chord length Am used to describe the domain size decreased; simultaneously, the distribution of Lambda trended to uniform as the mixing proceeded. After 2.0 min, Am fluctuated in a definite range. Further, a normalized distribution of dimensionless domain sizes Lambda/Lambda(m) was independent of mixing time, indicating that the late stage of phase dispersion can be scaled with a time-depended single length parameter Am. In other words, the morphology development shows a possible dynamic scaling behavior. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:561 / 572
页数:12
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