Title of article :
Structure, morphology and non-isothermal crystallization behavior of polypropylene catalloys
Author/Authors :
Zheng، نويسنده , , Qiang and Shangguan، نويسنده , , Yonggang and Yan، نويسنده , , Shouke and Song، نويسنده , , Yihu and Peng، نويسنده , , Mao and Zhang، نويسنده , , Qibin، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2005
Pages :
12
From page :
3163
To page :
3174
Abstract :
The structure, morphology and non-isothermal crystallization behavior of polypropylene catalloys (PP-cats) as well as pure polypropylene were investigated via differential scanning calorimeter (DSC), wide angle X-ray diffraction (WAXD) and real-time hot-stage optical microscopy (OM). The results reveal that the crystalline structures of PP-cats change with variations of the crystallization conditions and composition. The crystalline phase might consist of α-PP, β-PP and PE crystals. The content of β-PP increases with the increase of EP copolymer content and the cooling rate. At lower cooling rates, the morphologies of all non-isothermal crystallized PP-cats show spherulitic structure, and the decrease of crystal perfection and the increase of nucleation density of PP-cats system could be evidently observed. Considering the compositions of PP-cats, these indicated that the interactions between propylene homopolymer and the ethylene–propylene copolymers (both random and block ones) are in favor of the enhancement of the nucleation ability of α-form as well as β-form. In comparison with pure PP, the overall crystallization rates of the PP-cats increase dramatically, while the growth rates of the spherulites in all PP-cats decrease distinctly under the given cooling conditions. These experimental results were explained on the basis of diluting effect and obstructing effect on the mobility of PP chains in the ethylene–propylene copolymer.
Keywords :
Non-isothermal crystallization , Polypropylene catalloys , morphology
Journal title :
Polymer
Serial Year :
2005
Journal title :
Polymer
Record number :
1722840
Link To Document :
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