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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1107658Erstellt: 24. Oktober 2026

Vinyl Chloride → Vinyl chloride-vinyl acetate

https://huagongshe.com/de/reaction/1107658

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVinyl ChlorideHCID 6338—
EduktVinyl AcetateHCID 7904—
EduktPeroxydicarbonic acid, C,C'-bis(2-ethylhexyl) esterHCID 85963—
LösungsmittelMethanolHCID 887—
ProduktVinyl chloride-vinyl acetateHCID 61927—

Reaktionsschritte

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, 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-N,N-dimethylethanolamine-modified vinyl unit copolymer powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06063500
Quelldatensatzuspto-grants-2000_05
ORD IDord-c36662992a3545c8b6b291a9d630e928
Quellennotizuspto-grants-2000_05