Influence of nanofillers on the deformation process in layered silicate/polyamide-12 nanocomposites

被引:264
作者
Kim, GM [1 ]
Lee, DH
Hoffmann, B
Kressler, J
Stöppelmann, G
机构
[1] Kyungpook Natl Univ, Dept Polymer Sci, Taegu 702701, South Korea
[2] Eindhoven Univ Technol, Dept Mech Engn, Dutch Polymer Inst, NL-5600 MB Eindhoven, Netherlands
[3] Univ Freiburg, Freiburger Mat Forschungszentrum, D-79104 Freiburg, Germany
[4] Univ Freiburg, Inst Makromol Chem, D-79104 Freiburg, Germany
[5] Univ Halle Wittenberg, Fachbereich Ingenieurwissensch, D-06099 Halle, Germany
[6] EMS CHEMIE AG, CH-7013 Domat Ems, Switzerland
关键词
layered silicate; polyamide-12; deformation process;
D O I
10.1016/S0032-3861(00)00468-7
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polymer nanocomposites based on a synthetic layered silicate and polyamide-12 (PA-12) are prepared by injection molding to study their morphology, and the influence of nanofiller particles on local deformation processes. One of the most striking results from morphological studies by transmission electron microscopy is that although the layered silicates, locally stacked in the PA-12 matrix, are arranged on planes parallel to the injection molding direction, the fine lamellae are oriented with their planes perpendicular to the injection molding direction owing to nucleation at the interface between layered silicate and polymer matrix. The dispersion of layered silicates and the orientation of lamellae are reflected in the complexity of the deformation mechanisms, which in turn determine the ultimate macroscopic properties. From studies of in situ deformation under the high voltage electron microscope, it is concluded that the main deformation mechanism is microvoid formation inside the stacks of layered silicates. According to the orientation of these stacks the applied energy is dissipated by splitting, opening or sliding of separate bundles in the stacks during deformation. The nanofiller particles are load-bearing because surfaces in the microvoids are connected and hinder further growth of the microvoids, thus preventing catastrophic failure. As a consequence, the stiffness/strength/toughness balance has been synergistically improved. Finally, based on the present experimental results, a molecular network in polymer nanocomposites is proposed, that leads to the desired superfunctional characteristics. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1095 / 1100
页数:6
相关论文
共 43 条
[1]  
[Anonymous], 1968, CLAY MINER
[2]   DEFORMATION MECHANISMS AND PLASTIC RESISTANCE IN SINGLE-CRYSTAL-TEXTURED HIGH-DENSITY POLYETHYLENE [J].
BARTCZAK, Z ;
ARGON, AS ;
COHEN, RE .
MACROMOLECULES, 1992, 25 (19) :5036-5053
[3]   Redox polymerisation of acrylamide on aqueous montmorillonite surface: kinetics and mechanism of enhanced chain growth [J].
Bera, P ;
Saha, SK .
POLYMER, 1998, 39 (6-7) :1461-1469
[4]   POLYMERIZATION OF MONOLAYERS .6. INFLUENCE OF NATURE OF EXCHANGEABLE ION ON TACTICITY OF INSERTION POLY(METHYL METHACRYLATE) [J].
BLUMSTEIN, A ;
PARIKH, KK ;
MALHOTRA, SL ;
BLUMSTEIN, R .
JOURNAL OF POLYMER SCIENCE PART A-2-POLYMER PHYSICS, 1971, 9 (09) :1681-+
[5]  
Bovey FA, 1979, MACROMOLECULES INTRO
[6]  
BRIDLEY SW, 1980, CRYSTAL STRUCTURE CL
[7]   TOPOCHEMICAL DIACETYLENE POLYMERIZATION IN LAYERED METAL PHOSPHATE SALTS [J].
CAO, G ;
MALLOUK, TE .
JOURNAL OF SOLID STATE CHEMISTRY, 1991, 94 (01) :59-71
[8]   MORPHOLOGY OF CACO3-FILLED POLYETHYLENES [J].
CHACKO, VP ;
KARASZ, FE ;
FARRIS, RJ ;
THOMAS, EL .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1982, 20 (12) :2177-2195
[9]  
*CO OP CHEM CO LTD, SYNTH MIC MICR
[10]  
FRIEDRICH K, 1983, FIBRE SCI TECHNOL, V18, P34