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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1361567생성일: 2026년 10월 25일

Ethylene → Ethene propene 1-butene

https://huagongshe.com/reaction/1361567

반응식

참여 물질

역할이름HCID투입량
반응물EthyleneHCID 6325—
반응물1-ButeneHCID 7844—
반응물PropyleneHCID 8252—
반응물AluminumHCID 5359268—
반응물TriisobutylaluminumHCID 16682931—
촉매HCID 178436248HCID 178436248—
용매MethanolHCID 887—
용매TolueneHCID 1140—
용매HexaneHCID 8058—
생성물Ethene propene 1-buteneHCID 168434—

반응 조건

온도55 °C

반응 단계

To a 2000 ml polymerization apparatus dried under reduced pressure and thoroughly purged with nitrogen, 817 ml of dry hexane, 50 g of 1-butene and triisobutylaluminum (1.0 mmol) were charged at normal temperature, then the temperature inside the polymerization apparatus was elevated to 55° C., and the polymerization apparatus was pressurized with propylene to 0.70 MPa and subsequently pressurized with ethylene to 0.75 MPa. Thereafter, a toluene solution in which 0.001 mmol of diphenylmethylene(3-tert-butyl-5-ethylcyclopentadienyl) (2,7-ditert-butyl-fluorenyl)zirconium dichloride synthesized by Synthesis Method 4 and methylaluminoxane (manufactured by Tosoh Finechem Corp.) in terms of 0.3 mmol of aluminum were contacted, was added to the polymerization vessel, and polymerization was conducted for 25 minutes while maintaining the internal temperature at 55° C. and the total pressure at 0.75 MPa by continuously supplying ethylene. The polymerization was stopped by adding 20 ml of methanol. After depressurizing, a polymer was precipitated out of the polymerization solution in 2 L of methanol, and was dried in a vacuum at 130° C. for 12 hours. The obtained polymer was 46.1 g and the polymerization activity was 110.7 kg/mmol-cat-hr. The polymer had a composition of 74.5 mol % of propylene content, 17.5 mol % of ethylene content and 8.0 mol % of 1-butene content, and had an intrinsic viscosity [η] of 2.98 dl/g. Triad isotacticity was 94%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879960B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-5291282436a44486be3e99f3936fc90e
출처 메모uspto-grants-2011_02