The β-crystalline form of isotactic polypropylene in blends of isotactic polypropylene and polyamide-6/clay nanocomposites

被引:32
作者
Feng, M
Gong, FL
Zhao, CG
Chen, GM
Zhang, SM
Yang, MS [1 ]
Han, CC
机构
[1] Chinese Acad Sci, Inst Chem, Joint Lab Polymer Sci & Mat, Key Lab Engn Plast,Chinese Acad Sci, Beijing 100080, Peoples R China
[2] Chinese Acad Sci, Joint Lab Polymer Sci & Mat, State Key Lab Polymer Phys & Chem, Beijing 100080, Peoples R China
关键词
blends; clay; crystalline form; isotactic polypropylene; nanocomposites; polyamide-6;
D O I
10.1002/polb.20214
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Blends of isotactic polypropylene and polyamide-6/clay nanocomposites (iPP/NPA6) were prepared with an internal batch mixer. A high content of the beta-crystalline form of isotactic polypropylene (beta-iPP) was observed in the injection-molded samples of the iPP/NPA6 blends, whereas the content of beta-iPP in the iPP/PA6 blends and the iPP/clay composite was low and similar to that of neat iPP. Quiescent melt crystallization was studied by means of wide-angle X-ray diffraction, differential scanning calorimetry, and polarized optical microscopy. We found that the significant beta-iPP is not formed during quiescent melt crystallization regardless of whether the sample used was the iPP/NPA6 blend or an NPA6 fiber/iPP composite. Further characterization of the injection-molded iPP/NPA6 revealed a shear-induced skin-core distribution of beta-iPP and the formation of beta-iPP in the iPP/NPA6 blends is related to the shear flow field during cavity-filling. In the presence of clay, the deformation ability of the NPA6 domain is decreased, as evidenced by rheological and morphological studies. It is reasonable that the enhanced relative shear, caused by low deformability of the NPA6 domain in the iPP matrix, is responsible for beta-iPP formation in the iPP/NPA6 blends. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:3428 / 3438
页数:11
相关论文
共 39 条
[1]   Enhanced adhesion between polypropylene and polyamide-6: Role of interfacial nucleation of the beta-crystalline form of polypropylene [J].
Boucher, E ;
Folkers, JP ;
Creton, C ;
Hervet, H ;
Leger, L .
MACROMOLECULES, 1997, 30 (07) :2102-2109
[2]   Compatibilizing effect of maleated polypropylene on the mechanical properties and morphology of injection molded polyamide 6/polypropylene/organoclay nanocomposites [J].
Chow, WS ;
Ishak, ZAM ;
Karger-Kocsis, J ;
Apostolov, AA ;
Ishiaku, US .
POLYMER, 2003, 44 (24) :7427-7440
[3]   The use of clay in an EVA-based intumescent formulation. Comparison with the intumescent formulation using polyamide-6 clay nanocomposite as carbonisation agent [J].
Dabrowski, F ;
Le Bras, M ;
Cartier, L ;
Bourbigot, S .
JOURNAL OF FIRE SCIENCES, 2001, 19 (03) :219-241
[4]   Thermal behavior and morphological and rheological properties of polypropylene and novel elastomeric ethylene copolymer blends [J].
Di, YW ;
Iannace, S ;
Nicolais, L .
JOURNAL OF APPLIED POLYMER SCIENCE, 2002, 86 (13) :3430-3439
[5]  
FENG M, IN PRESS POLYM INT
[6]   Crystallization behavior of nylon 6 nanocomposites [J].
Fornes, TD ;
Paul, DR .
POLYMER, 2003, 44 (14) :3945-3961
[7]   Polymorphism of isotactic polypropylene in presence of additives, in blends and in composites [J].
Garbarczyk, J ;
Paukszta, D ;
Borysiak, S .
JOURNAL OF MACROMOLECULAR SCIENCE-PHYSICS, 2002, B41 (4-6) :1267-1278
[8]  
KargerKocsis J, 1996, J APPL POLYM SCI, V62, P291, DOI 10.1002/(SICI)1097-4628(19961010)62:2<291::AID-APP4>3.0.CO
[9]  
2-S
[10]   The effect of specific β-nucleation on morphology and mechanical behavior of isotactic polypropylene [J].
Kotek, J ;
Raab, M ;
Baldrian, J ;
Grellmann, W .
JOURNAL OF APPLIED POLYMER SCIENCE, 2002, 85 (06) :1174-1184