HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 485738Erstellt: 25. Oktober 2026
Styrene → Benzene, ethenyl-, polymer with 1,3-butadiene
https://huagongshe.com/reaction/485738
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Styrene | HCID 7501 | — |
| Edukt | 1,3-Butadiene | HCID 7845 | — |
| Edukt | Triphenylphosphine Oxide | HCID 13097 | — |
| Edukt | Phenol, bis(1,1-dimethylethyl)-4-methyl- | HCID 3034427 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | Styrene | HCID 7501 | 19,4% |
| Produkt | Benzene, ethenyl-, polymer with 1,3-butadiene | HCID 62697 | 40,9% |
Reaktionsschritte
A one gallon stainless steel reactor equipped with a stirrer blade is charged with 95 grams of 1,3-butadiene and 19 grams of styrene in 2,000 grams of n-hexane. One-half millimoles of TPPO are added and the temperature is adjusted to 100° C. One millimole of n-butyllithium is added to the mixture in the reaction vessel. Polymerization is completed within 30 minutes with the final maximum reaction temperature reaching 130° C. After termination of the reaction, 0.5 percent by weight of an antioxidant, di-tert-butyl-p-cresol ("IONOL"), based on the reaction mixture, is added to the mixture which is coagulated in isopropanol and drum dried to remove the solids. The initial monomer charge underwent a 93 percent conversion to form the product butadiene-styrene copolymer containing 40.9 percent of 1,2-microstructure and 19.4 percent of styrene as determined by IR spectroscopy.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04537939 |
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| Quelldatensatz | uspto-grants-1985_08 |
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| ORD ID | ord-9553bc95d6e64b4bb0b86d903f6659f1 |
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| Quellennotiz | uspto-grants-1985_08 |
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