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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584702Generated: October 26, 2026

Vinyl Chloride → Vinyl chloride-vinyl acetate

https://huagongshe.com/reaction/1584702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl ChlorideHCID 6338—
ReactantVinyl AcetateHCID 7904—
ReactantPeroxydicarbonic acid, C,C'-bis(2-ethylhexyl) esterHCID 85963—
SolventMethanolHCID 887—
ProductVinyl chloride-vinyl acetateHCID 61927—

Reaction Steps

An autoclave equipped with a stirrer was charged with methanol, vinyl chloride, vinyl acetate, 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. Then, the resulting product was filtered and dried to obtain a vinyl chloride-vinyl acetate copolymer powder. This copolymer, methanol 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 copolymer powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935714
Source datasetuspto-grants-1999_08
ORD IDord-8003f7e39d66485d866413b3a3bfcd0a
Source noteuspto-grants-1999_08