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Syntheses and properties of graft polymers of N ‐substituted acrylamides onto EPDM
Author(s) -
Park KyoungGon,
Park JongGu,
Ha ChangSik,
Cho WonJei
Publication year - 1999
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/(sici)1097-4628(19991220)74:13<3259::aid-app29>3.0.co;2-i
Subject(s) - copolymer , benzoyl peroxide , materials science , polymer chemistry , epdm rubber , monomer , polymer , thermal decomposition , polymerization , grafting , toluene , moiety , chemistry , composite material , natural rubber , organic chemistry
The graft polymerizations of N ‐isopropylacrylamide (NIPAM) or N ‐phenylacrylamide (NPAM) onto ethylene‐propylene‐diene terpolymer (EPDM) were carried out with benzoyl peroxide (BPO) as an initiator in toluene or THF. The structures of synthesized graft polymers, EPDM‐ g ‐ N ‐isopropylacrylamide (ENIPAM) and EPDM‐ g ‐ N ‐phenylacrylamide (ENPAM), were identified by infrared (IR) spectroscopy. The effects of monomer concentration, reaction time, and initiator concentration were investigated on the graft polymerization. The highest graft efficiency of NIPAM was obtained at 0.75 mol/L of NIPAM, 4 g of EPDM, 3 wt % of BPO, and 70°C for 48 h and that of NPAM did not much change up to 0.75 mol/L of NPAM, 4 g of EPDM, 3 wt % of BPO, and 70°C for 72 h. The thermal decomposition temperatures, wettabilities, and tensile strengths of ENIPAM and ENPAM all decreased with an increasing concentration of NIPAM and NPAM moiety in the corresponding polymers, respectively. The morphologies of ENIPAM and ENPAM after irradiation showed many gel particles as compared with those of ENIPAM and ENPAM before irradiation. The UV light and 60 Co γ‐ray resistances of ENIPAM and ENPAM were worse than those of EPDM due to carbonyl group in NIPAM and NPAM. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 3259–3267, 1999