Radical copolymerization between methyl methacrylate and N-cyclohexylmaleimide with thiol as an inifer
β Scribed by Xulin Jiang; Deyue Yan; Xinyuan Zhu; Jin Lin; Ping Xia
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 162 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
N-dodecanethiol (RSH)
was found efficient to initiate the radical copolymerization of methyl methacrylate (MMA) with N-cyclohexylmaleimide (NCMI) at 40 -60Β°C. The initial copolymerization rate, R p , increases respectively with increasing [RSH] and the mol fraction of NCMI in the comonomer feed, f NCMI. The molecular weight of the copolymer decreases with increasing [RSH]. The initiator transfer constant of RSH was determined to be C I Ο 0.21. The apparent activation energy of the overall copolymerization was measured to be 46.9 kJ/mol. The monomer reactivity ratios were determined to be r NCMI Ο 0.32 and r MMA Ο 1.35. The glass transition temperature of the copolymer increases obviously with increasing f NCMI , which indicates that adding NCMI may improve the heat resistance of plexiglass.
π SIMILAR VOLUMES
The kinetics for the radical copolymerization of methyl methacrylate (MMA) with N-cyclohexylmaleimide (NCMI) was investigated. The initial copolymerization rate R p is proportional to the initiator concentration to the power of 0.54. The apparent activation energy of the overall copolymerization was
Two new monomers based on thioxanthone, 2-(3@-acryloxy)propoxythioxanthone (M-2) and 1-methyl-4-(3@-acryloxy)propoxythioxanthone (M-4), were prepared and their radical copolymerization at 70Β‘C with methyl methacrylate (MMA) was studied. By varying the conversion reached for a Γxed feed composition,