The copolymerization of zinc methacrylate (ZMA) and 2-(N-ethylperfluorooctanesulfonamide)ethyl acrylate (RFA) in benzene was studied as a model for the copolymerization of ZMA and RFA in synthetic rubber during the peroxide curing process (in situ copolymerization). To confirm copolymer formation fr
Copolymerization of zinc methacrylate and perfluoroalkyl acrylates in different solvents
✍ Scribed by Takaharu Ikeda; Bunichiro Yamada
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 139 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
The copolymerizations of zinc dimethacrylate (ZMA) and 2-(N-ethylperfluorooctanesulfonamide)ethyl acrylate (RfSA) in various solvents were carried out in relation to the copolymerization of ZMA and RfSA in a synthetic rubber during the peroxide curing process (in situ copolymerization). The ZMA-RfSA copolymerization initiated with 2,2Ј-azobisisobutyronitrile at an equimolar mixture of the monomers yielded a copolymer of which the composition was almost the same with that of the comonomer, regardless of the solvent used. It was considered that the sulfonamido group in monomeric RfSA and the copolymer of RfSA specifically improves the miscibility of RfSA with ZMA.
📜 SIMILAR VOLUMES
Radical copolymerizations of zinc dimethacrylate and 2-(N-ethylper¯uorooctanesulphonamido)ethyl acrylate initiated with di-t-butyl peroxy di-isopropylbenzene were carried out in various amounts of DMF for 10 h at 140 °C in the presence of hydrogenated nitrile-butadiene rubber (HNBR) as a simulation
## Abstract The reverse atom transfer radical polymerization of methyl methacrylate was investigated in different solvents: xylene, __N,N__‐dimethylformamide, and pyridine. The polymerizations were uncontrolled, using 2,2′‐bipyridine as a ligand in xylene and pyridine because the catalyst (CuBr~2~/