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Solid-state 19F NMR investigation of poly(vinylidene fluoride) with high-power proton decoupling

✍ Scribed by Peter Holstein; Robin K. Harris; Barry J. Say


Book ID
104357856
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
592 KB
Volume
8
Category
Article
ISSN
0926-2040

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✦ Synopsis


The use of high-power proton decoupling has enabled highly-resolved spectra of fluorine polymers to be recorded, as is exemplified herein for semicrystalline poly(vinylidene fluoride) (PVDF). By means of high MAS speeds (up to 17 kHz), the spinning sidebands are removed from the whole of the relevant chemical shift range. For spectra of the crystalline regions of the polymer, the high-power decoupling is necessary, though its effect is not large. Various relaxation techniques have been used to examine the semicrystallinity and the polymorphism of PVDF, with special pulse sequences used to discriminate between the various domains. Different chemical shifts have been observed for the signals of the amorphous and crystalline phases. Those of the more immobile parts cover a substantial range. 0 1997 Elsevier Science B.V.


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Triple-channel solid-state NMR investigations of two di †erent poly(vinylidene Γ‘uoride) (PVDF) materials are described. Carbon-13 cross-polarization magic angle spinning NMR spectra were recorded using simultaneous high-power decoupling on both the proton and Γ‘uorine channels. Both 1H to 13C and 19F