Comonomer sequence determination of vinyl acetate–glycidyl methacrylate copolymers by NMR spectroscopy
✍ Scribed by A. S. Brar; Shiv Charan
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 414 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
✦ Synopsis
SYNOPSIS
(Vinyl acetate)/(glycidyl methacrylate) (V/G) copolymers were prepared by free radical solution polymerization in benzene. Copolymer composition was determined by 'H-NMR spectroscopy. Comonomer reactivity ratios were calculated by Kelen-Tiidos (KT) and errorin-variables (EVM) methods. The values reactivity ratios calculated by these methods are rv = 0.03 -t 0.01; rG = 38.9 -t 6.20 (KT) and rv = 0.03 -t 0.002; rG = 39.5 k 1.97 (EVM). The microstructure of V/G copolymers in terms of the distribution of V and G centered was obtained from 13C{ 'H}-NMR spectra using the carbonyl carbon resonance signals of V as well as G units. 0
📜 SIMILAR VOLUMES
Methyl methacrylate/vinylidene chloride (M/V) copolymers of different monomer concentrations were prepared by photopolymerization using the uranyl ion as photosensitizer. The copolymer composition was determined by chlorine estimation of the copolymers. The complete assignment of the 13 C{ 1 H} NMR
## Abstract Copolymers of __N__‐vinyl‐2‐pyrrolidone (V) and glycidyl methacrylate (G) monomers of different compositions were prepared by free‐radical solution polymerization. The copolymer composition of these copolymers was determined with ^1^H‐NMR spectra. The reactivity ratios calculated from t
Capitalizing on the superior sensitivity of proton NMR, relatively rapid estimates of three parameters, namely, comonomer content, crystallinity, and long spacing, are determined for three ethylene/vinyl alcohol copolymers using solid-state proton NMR measurements. Multiple-pulse techniques are util