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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584701Generated: October 26, 2026

Vinyl Chloride → Vmch

https://huagongshe.com/reaction/1584701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl ChlorideHCID 6338—
ReactantVinyl AcetateHCID 7904—
ReactantPeroxydicarbonic acid, C,C'-bis(2-ethylhexyl) esterHCID 85963—
ReactantMaleic AcidHCID 444266—
SolventMethanolHCID 887—
ProductVmchHCID 44146496—

Reaction Steps

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935714
Source datasetuspto-grants-1999_08
ORD IDord-1a6fda23564240309dfd4b201b3fa3a3
Source noteuspto-grants-1999_08