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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1107656생성일: 2026년 10월 25일

Vinyl Chloride → Vmch

https://huagongshe.com/reaction/1107656

반응식

참여 물질

역할이름HCID투입량
반응물Vinyl ChlorideHCID 6338—
반응물Vinyl AcetateHCID 7904—
반응물Peroxydicarbonic acid, C,C'-bis(2-ethylhexyl) esterHCID 85963—
반응물Maleic AcidHCID 444266—
용매MethanolHCID 887—
생성물VmchHCID 44146496—

반응 단계

An autoclave equipped with a stirrer was charged with methanol, vinyl chloride, vinyl acetate, maleic acid, di(2-ethylhexyl) peroxydicarbonate and partially saponified polyvinyl alcohol, and the temperature was elevated to 60° C. with stirring under an atmosphere of nitrogen gas to initiate the reaction, followed by further continuous injection of vinyl chloride to conduct the copolymerization reaction. After release of the residual pressure of the autoclave and cooling, a copolymer slurry was taken out and filtered, followed by washing with methanol three times and further with deionized water twice, thus obtaining a vinyl chloride-vinyl acetate-maleic acid copolymer powder. This copolymer, methanol, N,N-dimethylethanolamine and sodium hydroxide were added to a reactor equipped with a cooling pipe, and were allowed to react at 40° C. Then, the reaction product was cooled, and acetic acid was added thereto to neutralize unreacted sodium hydroxide. The resulting product was washed with methanol three times and further with deionized water twice, followed by filtering and drying to obtain a vinyl chloride-vinyl acetate-vinyl alcohol-maleic acid-N,N-dimethylethanolamine-modified vinyl unit copolymer powder. Copolymers different in weight ratio of monomers shown in Table 1 were produced by changing the amounts of the respective monomer units or amine compounds.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06063500
출처 데이터셋uspto-grants-2000_05
ORD IDord-c86e94b6510c4e528f9aca513ba8e936
출처 메모uspto-grants-2000_05