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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385648Generated: October 31, 2026

Ethylene → Ethene propene 1-butene

https://huagongshe.com/reaction/1385648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyleneHCID 6325—
Reactant1-ButeneHCID 7844—
ReactantPropyleneHCID 8252—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178440520HCID 178440520—
SolventTolueneHCID 1140—
ProductEthene propene 1-buteneHCID 168434—

Reaction Steps

This experiment was carried out in a similar manner as Example 1, except that the reaction was a batch reaction. A 1-liter autoclave reactor was thoroughly apurged with nitrogen and then charged with 300 ml of dried toluene. Through the mass flow controller, ethylene, propylene. 1-butene and hydrogen were fed into the reactor at a ratio of 4000 cc/min, 3600 cc/min, 400 cc/min, and 400 cc/min, respectively. Methyl aluminoxane in toluene solution, 46.9 mg-atom, as aluminum atom, and 0.015 mg-atom, as Zr atom, of bis(isopropylcyclopentadienyl)zirconium dichloride in toluene solutions were injected at 50° C. and 15 psig pressure. After 3 hours, the reaction was quenched with 1% aq. HCl, then washed with aqueous 1M NaOH, followed by a large quantity of water. After stripping off toluene, the reaction gave 348 grams of liquid terpolymer. The polymerization conditions and physical properties of the reactor product are summarized in Table IV. The crude reactor product was thermally cracked as described in Example 3, followed by distilling off the light polymer through a Vigreux column. The residue was hydrogenated with 1 wt % of 10% Pd on active carbon. The final hydrogenated liquid terpolymer had a kinematic viscosity at 100° C. of 9.6 cSt and viscosity index of 158; Mn of 1006, Mw/Mn of 1.24. The composition of the terpolymer, determined by C-13 NMR, was 72 mole % of ethylene, 25 mole % of propylene, and 3 mole % of butene. The physical properties are summarized in Table V.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262324B1
Source datasetuspto-grants-2001_07
ORD IDord-79cae5dbe1dc49b2aee96c062b614205
Source noteuspto-grants-2001_07