Crystalline structure of polyamide 12 as revealed by solid-state 13C NMR and synchrotron WAXS and SAXS

被引:65
作者
Dencheva, N
Nunes, TG
Oliveira, MJ
Denchev, Z [1 ]
机构
[1] Univ Minho, Inst Polymers & Composites, Dept Polymer Engn, P-4800058 Guimaraes, Portugal
[2] IST, Dept Mat Engn, P-1049001 Lisbon, Portugal
[3] IST, ICTPO, P-1049001 Lisbon, Portugal
关键词
annealing; crystallinity; polyamide; 12; solid-state NMR; synchrotron X-ray scattering;
D O I
10.1002/polb.20672
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 crystalline structure of polyamide-12 (PA12) was studied by solid-state C-13 nuclear magnetic resonance (NMR) as well as by synchrotron wide- and small-angle X-ray scattering (WAXS and SAXS). Isotropic and oriented PA12 showed different NMR spectra ascribed to gamma- and gamma'-crystalline modifications, respectively. On the basis of the position of the first diffraction peak, the isotropic gamma-form and the oriented gamma'-form were shown to be with hexagonal crystalline lattice at room temperature. When heated, the two PA12 polymorphs demonstrated different behaviors. Above 140 degrees C, the isotropic gamma-PA12 partially transformed into alpha-modification. No such transition was observed with the oriented gamma'-PA12 phase even after annealing at temperatures close to melting. A gamma'-gamma transition was observed here only after isotropization by melting point. Various structural parameters were extracted from the WAXS and SAXS patterns and analyzed as a function of temperature and orientation: the degree of crystallinity, the d-spacings, the Bragg's long spacings, the average thicknesses of the crystalline (l(c)) and amorphous (l(a)) phases, and the linear crystallinity x(cl) within the lamellar stacks. (c) 2005 Wiley Periodicals, Inc.
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页码:3720 / 3733
页数:14
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