참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Styrene | HCID 7501 | — |
| 반응물 | 1,3-Butadiene | HCID 7845 | — |
| 반응물 | Triphenylphosphine Oxide | HCID 13097 | — |
| 반응물 | Phenol, bis(1,1-dimethylethyl)-4-methyl- | HCID 3034427 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | Styrene | HCID 7501 | 19.4% |
| 생성물 | Benzene, ethenyl-, polymer with 1,3-butadiene | HCID 62697 | 40.9% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04537939 |
|---|
| 출처 데이터셋 | uspto-grants-1985_08 |
|---|
| ORD ID | ord-9553bc95d6e64b4bb0b86d903f6659f1 |
|---|
| 출처 메모 | uspto-grants-1985_08 |
|---|