Temperature dependence of polymer crystalline morphology in nylon 6/montmorillonite nanocomposites

被引:226
作者
Lincoln, DM
Vaia, RA [1 ]
Wang, ZG
Hsiao, BS
Krishnamoorti, R
机构
[1] USAF, Res Lab, Mat & Mfg Directorate, Wright Patterson AFB, OH 45433 USA
[2] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
[3] Univ Houston, Dept Chem Engn, Houston, TX 77004 USA
关键词
nylon; 6; nanocomposites; wide-angle X-ray scattering;
D O I
10.1016/S0032-3861(01)00542-0
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The influence of nanodispersed montmorillonite layers and process history on the crystal structure of nylon 6 between room temperature and melting is examined with simultaneous small- and wide-angle X-ray scattering and modulated differential scanning calorimetry. For the examined process history, nylon 6 exhibits predominantly alpha -phase behavior from room temperature to melting, with a gradual shift in chain-chain and sheet-sheet spacings from similar to 100 degreesC to melting. In contrast, the presence of aluminosilicate layers stabilizes a dominant gamma -crystal phase, which persists, essentially unmodified, until melting. The temperature dependence of the total crystallinity and the relative fractions of alpha- and gamma -phases is strongly dependent on the layered silicate content and the interaction between the nylon 6 and the aluminosilicate layers. Additionally, the temperature dependence of the alpha- and gamma -phases imply that the gamma -phase is preferentially in the proximity of the silicate layers, whereas the alpha -phase exists away from the polymer-silicate interphase region: In general, process history and use-temperature will determine the relative fraction of the crystalline polymer phases in semi-crystalline polymer nanocomposites, and thus have significant influence on the stability of the crystalline region at elevated temperatures. (C) 2001 Published by Elsevier Science Ltd.
引用
收藏
页码:9975 / 9985
页数:11
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