Micromechanical Processes and Failure Phenomena in Reactively Compatibilized Blends of Polyamide 6 and Styrenic Polymers. I. Polyamide 6/Acrylonitrile-Butadiene-Styrene Copolymer Blends

被引:4
作者
Handge, U. A. [1 ]
Sailer, C. [2 ]
Steininger, H. [3 ]
Weber, M. [4 ]
Scholtyssek, S. [5 ]
Seydewitz, V. [5 ]
Michler, G. H. [5 ]
机构
[1] Fac Engn Sci, Dept Polymer Engn, D-95447 Bayreuth, Germany
[2] ETH, Inst Polymers, Dept Mat, CH-8093 Zurich, Switzerland
[3] BASF SE, Polymer Res, GKP R G201, D-67056 Ludwigshafen, Germany
[4] BASF SE, Polymer Res, GKT B B1, D-67056 Ludwigshafen, Germany
[5] Univ Halle Wittenberg, Inst Phys, D-06099 Halle, Germany
基金
瑞士国家科学基金会;
关键词
blends; compatibilization; microdeformation; ACRYLONITRILE COPOLYMER; VISCOELASTIC PROPERTIES; MECHANICAL-PROPERTIES; TOUGHENED NYLON-6; RUBBER BLENDS; MORPHOLOGY; DEFORMATION; EVOLUTION; BEHAVIOR; FRACTURE;
D O I
10.1002/app.29566
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
hi this work, hi situ investigations of the micromechanical properties of reactively compatibilized blends of polyamide 6 (PA6) and an acrylonitrile-butadiene-styrene copolymer (ABS) were performed with transmission electron microscopy. Three PA6/ABS blends were prepared with a disperse morphology (inclusions of PA6 or ABS) and with a cocontinuous structure. The objective of this work was to study the deformation of the inclusions and the interface between the PA6 phase and the ABS phase. Our transmission electron microscopy investigations revealed that the morphology of the blends was strongly influenced by the asymmetric nature of the interface between PA6 and ABS. In the blends with a PA6 matrix, the interface between PA6 and the ABS inclusions was deformed in tensile deformation under uniaxial loading. A strong influence of the PA6 water content on the (micro)mechanical behavior was observed. Although the "dry" blends behaved in a brittle fashion, the "wet" blends behaved in a ductile fashion with the formation of deformation bands in the matrix (PA6 or ABS), which were initiated by stress concentration at the particles (ABS or PA6, respectively). (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 112:1658-1669, 2009
引用
收藏
页码:1658 / 1669
页数:12
相关论文
共 37 条
[1]
Interphase and compatibilization of polymer blends [J].
Ajji, A ;
Utracki, LA .
POLYMER ENGINEERING AND SCIENCE, 1996, 36 (12) :1574-1585
[2]
Rheological and mechanical properties of poly(α-methylstyrene-co-acrylonitrile)/poly(methylacrylate-co-methyl methacrylate) blends in miscible and phase-separated regimes of various morphologies -: Part IV.: Influence of the morphology on the mechanical properties (IUPAC technical report) [J].
Altstädt, V ;
Freitas, LD ;
Schubert, DW .
PURE AND APPLIED CHEMISTRY, 2004, 76 (02) :389-413
[4]
Effect of compatibilizer in acrylonitrile-butadiene-styrene toughened nylon 6 blends:: Ductile-brittle transition temperature [J].
Araújo, EM ;
Hage, E ;
Carvalho, AJF .
JOURNAL OF APPLIED POLYMER SCIENCE, 2003, 90 (10) :2643-2647
[5]
Acrylonitrile-butadiene-styrene toughened nylon 6:: The influences of compatibilizer on morphology and impact properties [J].
Araújo, EM ;
Hage, E ;
Carvalho, AJF .
JOURNAL OF APPLIED POLYMER SCIENCE, 2003, 87 (05) :842-847
[6]
Multicomponent blends based on polyamide 6 and styrenic polymers:: morphology and melt rheology [J].
Jafari, SH ;
Pötschke, P ;
Stephan, M ;
Warth, H ;
Alberts, H .
POLYMER, 2002, 43 (25) :6985-6992
[7]
Thermal behavior and morphology of polyamide 6 based multicomponent blends [J].
Jafari, SH ;
Pötschke, P ;
Stephan, M ;
Pompe, G ;
Warth, H ;
Alberts, H .
JOURNAL OF APPLIED POLYMER SCIENCE, 2002, 84 (14) :2753-2759
[8]
POLYAMIDE-RUBBER BLENDS - MICROSCOPIC STUDIES OF THE DEFORMATION ZONE [J].
JANIK, H ;
GAYMANS, RJ ;
DIJKSTRA, K .
POLYMER, 1995, 36 (22) :4203-4208
[9]
Premade vs. reactively formed compatibilizers for PMMA/PS melt blends [J].
Jeon, HK ;
Zhang, JB ;
Macosko, CW .
POLYMER, 2005, 46 (26) :12422-12429
[10]
Reactive compatibilization of nylon 6/styrene-acrylonitrile copolymer blends. Part 1. Phase inversion behavior [J].
Kitayama, N ;
Keskkula, H ;
Paul, DR .
POLYMER, 2000, 41 (22) :8041-8052