Vinyl acetate/butyl methacrylate ( V/B ) copolymers were prepared by free-radical solution polymerization in benzene. Compositions of the copolymers have been obtained from 'H-NMR spectroscopy. Kelen-Tudos (KT) , the nonlinear error in variables method (EVM) , and I3C { 'H 1 -NMR spectra of the copo
Reactivity ratios and thermal and dielectric studies of n-butyl methacrylate and methacrylamide copolymers
β Scribed by B. Srinivasulu; P. Raghunath Rao; E. V. Sundaram; G. Sathaiah; Lalitha Sirdeshmukh
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 380 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
Free-radical copolymerization of n-butyl methacrylate ( B ) and methacrylamide ( M ) was carried out in the presence of 2,2'-azobisisobutyronitrile ( AIBN ) in dimethyl formamide (DMF) at 60Β°C. The percentage composition of the copolymers was established by elemental analysis. The reactivity ratios as determined by the Finemann-Ross (F-R) and the Kelen-Tud6s (K-T) methods are rl ( B ) = 2.75 5 0.01, r2 ( M ) = 0.2 f 0.01 and r1 = 2.70 ? 0.05, r2 = 0.19 k 0.02, respectively. The copolymers were characterized by IR, 'H-NMR, thermal, and dielectric studies. Glass transition temperature ( T,) values were determined by DSC. Dielectric studies were carried out to understand the segmental motions and the effect of composition on dielectric loss.
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## Abstract Freeβradical copolymerization of 4βnitrophenyl acrylate (NPA) with __n__βbutyl methacrylate (BMA) was carried out using benzoyl peroxide as an initiator. Seven different mole ratios of NPA and BMA were chosen for this study. The copolymers were characterized by IR, ^1^HβNMR, and ^13^CβN
The synthesis, characterization, and thermal properties of copolymers of methyl methacrylate (MMA) and N-(p-carboxyphenyl) methacrylamide/acrylamide (CPMA/CPA) are described. The copolymerization was carried out in solution by taking different mole fractions (0.1-0.5) of CPMA/CPA in the initial feed