z-logo
Premium
Reactivity ratios and microstructure of vinyl acetate–butyl methacrylate copolymers: NMR study
Author(s) -
Brar A. S.,
Charan Shiv
Publication year - 1994
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.1994.070510411
Subject(s) - comonomer , copolymer , reactivity (psychology) , vinyl acetate , polymer chemistry , nuclear magnetic resonance spectroscopy , nmr spectra database , materials science , triad (sociology) , proton nmr , methacrylate , methyl methacrylate , spectroscopy , microstructure , polymerization , chemistry , crystallography , spectral line , organic chemistry , polymer , physics , medicine , psychology , alternative medicine , pathology , astronomy , psychoanalysis , quantum mechanics
Vinyl acetate/butyl methacrylate (V/B) copolymers were prepared by free‐radical solution polymerization in benzene. Compositions of the copolymers have been obtained from 1 H‐NMR spectroscopy. Kelen–Tüdös (KT), the nonlinear error in variables method (EVM), and 13 C{ 1 H}‐NMR spectra of the copolymers were utilized to calculate the comonomer reactivity ratios. The reactivity from different methods are r V = 0.06 ± 0.02, r B = 26.34 ± 8.49 (KT); r V = 0.06 ± 0.01, r B = 26.88 ± 3.59 (EVM); and r V = 0.06, r B = 18.20 ( 13 C‐NMR spectroscopy). The microstructure in terms of V‐ and B‐centered triad fractions was obtained using 13 C{ 1 H}‐NMR spectra of copolymers. The copolymerization behavior of V/B copolymers as a function of conversion was also studied. © 1994 John Wiley & Sons, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom