Journal
EUROPEAN POLYMER JOURNAL
Volume 38, Issue 7, Pages 1319-1326Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0014-3057(02)00019-8
Keywords
3,5-dimethylplienyl methacrylate; copolymerization; reactivity ratios; H-1-NMR spectra; C-13-NMR; glycidyl methacrylate; thermal studies
Categories
Ask authors/readers for more resources
The acrylic monomer, 3,5-dimethylphenyl methacrylate was synthesized by reacting 3,5-dimethylphenol dissolved in ethyl methyl ketone (EMK) with methacryloyl chloride in the presence of triethylamine. The homopolymer and various copolymers with glycidyl methacrylate were synthesized using free radical polymerization in EMK solution at 70 +/- 1 degreesC using benzoyl peroxide as initiator. The copolymers were characterized by FT-IR, H-1-NMR and C-13-NMR techniques. The molecular weights ((M) over bar (n) and (M) over bar (w)) and polydispersity indices were determined using gel permeation chromatography. The glass transition temperatures were determined by differential scanning calorimetry. Thermogravimetric analysis were performed in air. The solubilities of the polymers were tested in various polar and non-polar solvents. Copolymer compositions were determined using H-1-NMR spectra. The monomer reactivity ratios were determined by application of conventional linearisation methods such as Fineman-Ross, Kelen-Tildos and extended Kelen-Tudos. (C) 2002 Elsevier Science Ltd. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available