Real-time morphological observation of isotactic polypropylene and poly(ethylene-co-octene) rubber blend during temperature change

被引:0
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作者
Ono, Michio [1 ,2 ,4 ]
Nakajima, Ken [2 ]
Misawa, Mayumi [3 ]
Nishi, Toshio [2 ]
机构
[1] SunAllomer Ltd., Kawasaki Development Center, Kawasaki-Ku, Kawasaki, Kanagawa 210-0863, Japan
[2] Department of Organic and Polymeric Materials, Faculty of Engineering, Tokyo Institute of Technology, Meguro-Ku, Tokyo 152-8552, Japan
[3] Nihon Veeco K. K., Application Group Metrology, Chuou-Ku, Tokyo104-0045, Japan
[4] Dow Japan Development Center, Dow Chemical Japan Ltd., 8-1, Ukishima-Cho, Kawasaki-Ku, Kawasaki-Shi, Kanagawa-Ken, 210-0862, Japan
来源
Journal of Applied Polymer Science | 2008年 / 108卷 / 03期
关键词
In the injection- and compression-molded specimens composed of isotactic polypropylene (iPP) and poly(ethylene-co-octene) rubber (EOR) blend; its morphological changes with temperature variation were investigated using an atomic force microscopy equipped with a heater accessory. Phase-separated sea-island structures comprising the iPP matrix (sea) and the EOR domains (island) were clearly observed in both specimens. In the injection-molded specimen; the morphology of the EOR domains was fibrous along flow direction (FD). In the iPP matrix; a stripelike structure consisting of alternating iPP crystalline lamellae and amorphous region was clearly observed at room temperature. As increasing temperatures; the iPP amorphous regions seemed to shrink gradually and could not be identified at 80°C. By contrast; in the compression-molded specimen; the EOR domains were circular in shape; and the alternate structure comprising the iPP crystal lamellae and amorphous regions was also found. At elevated temperatures; the iPP amorphous regions gradually enlarged. The analysis of the apparent activation energy obtained by a dynamic mechanical thermal analysis revealed that the differences in the morphological behavior in the iPP matrix region between the both specimens were attributed to the differences in the mobility in the iPP crystal regions. © 2008 Wiley Periodicals; Inc;
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页码:1857 / 1864
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