HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107658Generated: October 25, 2026
Vinyl Chloride → Vinyl chloride-vinyl acetate
https://huagongshe.com/reaction/1107658
Participants
| Role | Name | HCID | Charge |
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| Reactant | Vinyl Chloride | HCID 6338 | — |
| Reactant | Vinyl Acetate | HCID 7904 | — |
| Reactant | Peroxydicarbonic acid, C,C'-bis(2-ethylhexyl) ester | HCID 85963 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Vinyl chloride-vinyl acetate | HCID 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, 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06063500 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-c36662992a3545c8b6b291a9d630e928 |
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| Source note | uspto-grants-2000_05 |
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