Effect of isotactic polypropylene on crystal structure and morphology of β-modified random copolymerized polypropylene

被引:7
作者
Jiang, Nan [1 ]
Wang, Kailong [1 ]
Leng, Jinhua [2 ]
He, Bobing [1 ,2 ]
机构
[1] Sichuan Univ, Coll Chem, Chengdu 610064, Sichuan, Peoples R China
[2] Chong Qing Acad Metrol & Qual Inspect, Chongqing 401121, Peoples R China
关键词
Isotactic polypropylene; Polypropylene random copolymer; beta-Crystallization; Crystallization structure; NUCLEATING-AGENT; CRYSTALLIZATION BEHAVIOR; IMPACT; SHEAR; TEMPERATURE; PROPYLENE; PHASE;
D O I
10.1007/s00289-017-2244-3
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
It is difficult for the direct addition of beta-nucleating agents to obtain high contents of beta-crystals because of the effect of the random copolymer structure of random copolymerized polypropylene (PPR). In this study, the beta-crystallinity of PPR was improved by introducing a small amount of isotactic polypropylene (iPP) into beta-modified PPR. After optimizing the conditions, the degree of crystallinity increased to 56.5%, while the relative content of beta-crystal was as high as 92.4% and its beta-crystallinity increased by 61.5%. Its crystallization growth process showed that iPP first forms beta-nuclei and further induced PPR to produce beta-crystals. Due to the high content of beta crystal, toughness had been greatly improved. The impact test was carried out at - 15, 0, and 23 A degrees C, the impact strength of pure PPR was 2.3, 3.8, and 22.8 kJ/m(2), respectively. After adding 20 wt% iPP in beta-modified PPR, the impact strength increased to 3.3, 7.7 kJ/m(2), and 45.9 kJ. In addition, its elongation at break reached 574.4%, which is four times of the elongation at pure PPR. The self-rigid and high-content beta-crystals of iPP molecular chains have synergistic effect, which makes the tensile strength of the composite system almost unchanged. This study provides a method to regulate the structure and molecular chain activity of PPR crystal, which lays the foundation for the improvement of PPR performance.
引用
收藏
页码:4085 / 4101
页数:17
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