Crystallization and thermal behavior of microcellular infection-molded polyamide-6 nanocomposites

被引:20
作者
Yuan, Mingjun
Turng, Lih-Sheng [1 ]
Caulfield, Daniel F.
机构
[1] Univ Wisconsin, Ctr Polymer Engn, Madison, WI 53706 USA
[2] USDA, Forest Prod Lab, Madison, WI 53726 USA
关键词
D O I
10.1002/pen.20558
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This article presents the effects of nanoclay and supercritical nitrogen on the crystallization and thermal behavior of microcellular injection-molded polyamide-6 (PA6) nanocomposites with 5 and 7.5 wt% nanoclay. Differential scanning calorimetry (DSC), X-ray diffractometry (XRD), and polarized optical microscopy (POM) were used to characterize the thermal behavior and crystalline structure. The isothermal and nonisothermal crystallization kinetics of neat resin and its corresponding nanocomposite samples were analyzed using the Avrami and Ozawa equations, respectively. The activation energies determined using the Arrhenius equation for isothermal crystallization and the Kissinger equation for nonisothermal crystallization were comparable. The specimen thickness had a significant influence on the nonisothermal crystallization especially at high scanning rates. Nanocomposites with an optimal amount of nanoclay possessed the highest crystallization rate and a higher level of nucleation activity. The nanoclay increased the magnitude of the activation energy but decreased the overall crystallinity. The dissolved SCF did not alter the crystalline structure significantly. In contrast with conventionally injection-molded solid counterparts, microcellular neat resin parts and microcellular nanocomposite parts were found to have lower crystallinity in the core and higher crystallinity near the skin.
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收藏
页码:904 / 918
页数:15
相关论文
共 45 条
[21]   The effect of pressure and clay on the crystallization behavior and kinetics of polyamide-6 in nanocomposites [J].
Kamal, MR ;
Borse, NK ;
Garcia-Rejon, A .
POLYMER ENGINEERING AND SCIENCE, 2002, 42 (09) :1883-1896
[22]   COMMENTS AND RECOMMENDATIONS ON THE USE OF THE AVRAMI-EQUATION FOR PHYSICOCHEMICAL KINETICS [J].
KHANNA, YP ;
TAYLOR, TJ .
POLYMER ENGINEERING AND SCIENCE, 1988, 28 (16) :1042-1045
[23]   VARIATION OF PEAK TEMPERATURE WITH HEATING RATE IN DIFFERENTIAL THERMAL ANALYSIS [J].
KISSINGER, HE .
JOURNAL OF RESEARCH OF THE NATIONAL BUREAU OF STANDARDS, 1956, 57 (04) :217-221
[24]  
Kohan M.I., 1995, NYLON PLASTICS HDB
[25]  
Kolmogorov A., 1937, Izv. Ross. Akad. Nauk. Seriya Mat., V1, P335
[26]   Shear-enhanced crystallization in isotactic polypropylene. 3. Evidence for a kinetic pathway to nucleation [J].
Kumaraswamy, G ;
Kornfield, JA ;
Yeh, FJ ;
Hsiao, BS .
MACROMOLECULES, 2002, 35 (05) :1762-1769
[27]  
Lambert S.M., 1991, The Journal of Supercritical Fluids, V4, P15
[28]   Secondary structure and elevated temperature crystallite morphology of nylon-6/layered silicate nanocomposites [J].
Lincoln, DM ;
Vaia, RA ;
Wang, ZG ;
Hsiao, BS .
POLYMER, 2001, 42 (04) :1621-1631
[29]   Time-resolved shear behavior of end-tethered Nylon 6-clay nanocomposites followed by non-isothermal crystallization [J].
Medellin-Rodriguez, FJ ;
Burger, C ;
Hsiao, BS ;
Chu, B ;
Vaia, R ;
Phillips, S .
POLYMER, 2001, 42 (21) :9015-9023
[30]   KINETICS OF NON-ISOTHERMAL CRYSTALLIZATION [J].
OZAWA, T .
POLYMER, 1971, 12 (03) :150-&