Crystallization behavior of polymer/montmorillonite nanocomposites. Part III. Polyamide-6/montmorillonite nanocomposites, influence of matrix molecular weight, and of montmorillonite type and concentration

被引:75
作者
Homminga, DS [1 ]
Goderis, B [1 ]
Mathot, VBF [1 ]
Groeninckx, G [1 ]
机构
[1] Catholic Univ Louvain, Dept Chem, Div Mol & Nanomat, Lab Macromol & Struct Chem, B-3000 Heverlee, Belgium
关键词
polyamides; nanocomposite; extrusion;
D O I
10.1016/j.polymer.2005.10.141
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Several series of polyamide-6 (PA-6) nanocomposites, differing in montmorillonite (MMT) type and content and PA-6 matrix molecular weight, were prepared by melt-extrusion and the associated PA-6 crystallization behavior and morphology was evaluated using (synchrotron) Xray diffraction, transmission electron microscopy and differential scanning calorinietry. The nucleating ability of silicate layers is poor in PA-6 nanocomposites made by melt-extrusion because highly active, stable PA-6 crystallization precursors are generated during melt-extrusion. In most of the studied PA-6/MMT nanocomposites the dispersed silicate layers act as impurities and decrease rather than increase the overall crystallization kinetics of PA-6, especially at high MMT contents. Furthermore, at a given MMT concentration, the crystal growth retardation inflates with increasing degree of exfoliation, which dependents on the MMT type and which increases with increasing PA-6 molecular weight. One of the considered MMT types leads to a poorly exfoliatcd nanomorphology and as a result no retardation of crystal growth is observed. furthermore, the disturbed crystal growth does not alter the PA-6 semicrystalline stack morphology. Moderate nucleation effects due to the presence of MMT can be observed when the particle load is low (low amount of MMT and/or poor degree of exfoliation) and provided the supercooling is Sufficiently large. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1630 / 1639
页数:10
相关论文
共 34 条
[1]   Polymer-layered silicate nanocomposites: Preparation, properties and uses of a new class of materials [J].
Alexandre, Michael ;
Dubois, Philippe .
Materials Science and Engineering: R: Reports, 2000, 28 (1-2) :1-63
[2]  
BRANDRUP J, 1989, POLYM HDB, pCH6
[3]   Effect of melt processing conditions on the extent of exfoliation in organoclay-based nanocomposites [J].
Dennis, HR ;
Hunter, DL ;
Chang, D ;
Kim, S ;
White, JL ;
Cho, JW ;
Paul, DR .
POLYMER, 2001, 42 (23) :9513-9522
[4]   SELF-NUCLEATION AND ENHANCED NUCLEATION OF POLYMERS - DEFINITION OF A CONVENIENT CALORIMETRIC EFFICIENCY SCALE AND EVALUATION OF NUCLEATING ADDITIVES IN ISOTACTIC POLYPROPYLENE (ALPHA-PHASE) [J].
FILLON, B ;
LOTZ, B ;
THIERRY, A ;
WITTMANN, JC .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1993, 31 (10) :1395-1405
[5]   Crystallization behavior of nylon 6 nanocomposites [J].
Fornes, TD ;
Paul, DR .
POLYMER, 2003, 44 (14) :3945-3961
[6]   Nylon 6 nanocomposites: the effect of matrix molecular weight [J].
Fornes, TD ;
Yoon, PJ ;
Keskkula, H ;
Paul, DR .
POLYMER, 2001, 42 (25) :9929-9940
[7]   Primary and secondary crystallization in a homogeneous ethylene-1-octene copolymer: Crystallinity heterogeneity studied by SAXS [J].
Goderis, B ;
Reynaers, H ;
Koch, MHJ .
MACROMOLECULES, 2002, 35 (15) :5840-5853
[8]  
GODERIS B, 2005, COLLOID POLYM SCI, V130, P1
[9]   CRYSTALLIZATION OF POLY(ETHYLENE TEREPHTHALATE) INDUCED BY INORGANIC-COMPOUNDS .1. CRYSTALLIZATION BEHAVIOR FROM GLASSY STATE IN A LOW-TEMPERATURE REGION [J].
GROENINCKX, G ;
BERGHMANS, H ;
OVERBERGH, N ;
SMETS, G .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1974, 12 (02) :303-316
[10]   Influence of shear flow on the preparation of polymer layered silicate nanocomposites [J].
Homminga, D ;
Goderis, B ;
Hoffman, S ;
Reynaers, H ;
Groeninckx, G .
POLYMER, 2005, 46 (23) :9941-9954