HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethylene → Ethylene/Vinyl Acetate Maleic Anhydride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethylene | HCID 6325 | — |
| Edukt | Boron trifluoride | HCID 6356 | — |
| Edukt | Azobisisobutyronitrile | HCID 6547 | — |
| Edukt | Maleic Anhydride | HCID 7923 | — |
| Edukt | Ethyl Acrylate | HCID 8821 | — |
| Edukt | Allyl acrylate | HCID 13835 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Ethylene/Vinyl Acetate Maleic Anhydride | HCID 86650683 | — |
Reaktionsschritte
A 7.57-liter stirred autoclave was charged under nitrogen with 4000 ml of methylene chloride, 400 grams of ethyl acrylate, 20 grams of maleic anhydride, 1.2 grams of allyl acrylate, and 1.0 gram of azobis(isobutyronitrile). It was then sealed, charged with 300 grams of boron trifluoride, and pressured to 21 kg/sq cm with ethylene. The subsequent copolymerization at 25° C was continued until pressure measurement indicated that ethylene uptake had ceased (about two hours later). The reaction was quenched by addition of one liter of diethyl ether. Volatiles were removed by steam-stripping in a well-ventilated hood. The terpolymer thereby obtained was dissolved in acetone, precipitated in water in a blender, and oven-dried. Yield: 415 grams.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04017557 |
| Quelldatensatz | uspto-grants-1977_04 |
| ORD ID | ord-f88b54dc5bad4ad7954b4918d8518aa1 |
| Quellennotiz | uspto-grants-1977_04 |