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.
引用
收藏
页码:3720 / 3733
页数:14
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