Determination of polymer crystallinity by the multivariable curve resolution method in 13C solid NMR spectrum

被引:1
|
作者
Zhou, Xiaoyue
Xu, Kaipin
Ni, Pei
Chen, Qun [1 ]
Zhang, Shanmin [1 ]
机构
[1] East China Normal Univ, Phys Dept, 3663 North Zhong Shan Rd, Shanghai 200062, Peoples R China
关键词
Spin-lattice relaxation; Multi-curve resolution; Peak overlapping; Polymer crystallinity; MOLECULAR-WEIGHT POLYETHYLENE; CROSS-POLARIZATION; STATE NMR; RESONANCE TRANSIENTS; RECIPROCITY RELATION; RAMAN-SPECTROSCOPY; X-RAY; DYNAMICS; FIBERS; DOSY;
D O I
10.1016/j.ssnmr.2017.04.005
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Most of the polymers are composed of a crystal part, an amorphous part, and a transitional interfacial part. These components present disparate physical and chemical characteristics. However, it always suffers from peak overlapping in solid NMR spectrum in order to acquire polymer's crystallinity. The polyethylene oxide (PEO) sample was tested using the Torchia pulse sequence combined with the Multivariate Curve Resolution (MCR) method. A two dimensional CP/MAS spectrum containing spin-lattice relaxation time (T-1) information was acquired. After the correction based on the reciprocity relation, the overlapped peaks were resolved and quantified together with their T-1's. Crystallinity is therefore observed naturally according to components' content ratios associated with their T-1 values.
引用
收藏
页码:34 / 40
页数:7
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