IP Library Granted Patent US 10,919,819
Granted Patent B2
US 10,919,819 · App. 16/317,579 · Granted Feb 16, 2021

Oligomerization of ethylene

Inventors: Sudevan Sujith (Daejeon, KR); So Hee Sim (Daejeon, KR); Hyo Seung Park (Daejeon, KR); Sun Young Kim (Daejeon, KR); Sang Ick Lee (Daejeon, KR); Han Sol Lee (Daejeon, KR)
Assignees: SK Innovation Co., Ltd.; SK Global Chemical Co., Ltd.
C07C2/36B01J31/143B01J31/2409C07C2/08C07F9/28C08F4/69086C08F10/02B01J2231/20B01J2531/007B01J2531/62C07C2/24C07C2/32C07C2531/14C07C2531/24C08F2/06Y02P20/52
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,919,819
App. No.
16/317,579
Granted
Feb 16, 2021
Kind
B2
Abstract

Provided is a method for oligomerization of ethylene, and more particularly, a method for producing 1-hexene and 1-octene at a high selectivity under an ethylene atmosphere by inducing a remarkably improved catalytic activity while effectively reducing a production amount of polyethylene by introducing the oligomerization catalyst and a cocatalyst mixture containing at least two aluminums together and adjusting the kind of oligomerization catalyst and injection conditions thereof.

Claims (24)

1. A method for oligomerization of ethylene, the method comprising:

mixing an aluminoxane and an alkyl aluminum compound to prepare a cocatalyst mixture;

introducing the cocatalyst mixture and a oligomerization catalyst including a transition metal into a reactor;

introducing ethylene into the reactor; and

reacting the oligomerization catalyst, the cocatalyst mixture, and the ethylene in the reactor with each other,

wherein the oligomerization catalyst is a complex in which the transition metal and a heteroatom ligand represented by Chemical Formula 2 below are coordinated to each other

where, in Chemical Formula 2, R 11 to R 14 are each independently substituted or unsubstituted hydrocarbyl or substituted or unsubstituted heterohydrocarbyl; and

R 15 and R 16 are each independently substituted or unsubstituted hydrocarbyl, or R 15 and R 16 may be bonded to each other to form a ring.

2. The method of claim 1 , wherein the aluminoxane is methylaluminoxane or modified methylaluminoxane, and

the alkyl aluminum compound is one or more selected from isobutylaluminoxane, tetraisobutylaluminoxane, trimethylaluminum, triethylaluminum, tripropylaluminum, triisobutylaluminum, diisobutylaluminum, and trioctylaluminum.

3. The method of claim 1 , wherein R 15 and R 16 are bonded to each other to form an alicyclic ring or aromatic ring.

4. The method of claim 1 , wherein the transition metal is chromium.

5. The method of claim 1 , wherein the cocatalyst mixture is introduced into the reactor at a range from 1 to 10000 moles based on 1 mole of the oligomerization catalyst.

6. The method of claim 1 , wherein the cocatalyst mixture includes the aluminoxane and the alkyl aluminum compound at a molar ratio of 1:0.01 to 1:100.

7. The method of claim 1 , wherein the reacting is performed in the presence of hydrogen.

8. The method of claim 1 , wherein the reacting is performed at a temperature range from 0 to 200° C.

9. The method of claim 8 , wherein the reacting is performed at a temperature range from 20 to 100° C.

10. The method of claim 1 , wherein the reacting is performed at a pressure range from 1 to 500 bar.

11. The method of claim 1 , wherein 1-hexene, 1-octene, or a mixture thereof is selectively produced.

12. The method of claim 1 , further comprising:

mixing the cocatalyst mixture and the oligomerization catalyst before introducing the cocatalyst mixture and the oligomerization catalyst into the reactor.

13. The method of claim 1 , wherein the introducing the cocatalyst mixture and the oligomerization catalyst includes:

introducing the cocatalyst mixture into the reactor; and

introducing the oligomerization catalyst into the reactor.

Assignments (2)
CHANGE OF NAME Recorded Sep 2, 2022
From: SK GLOBAL CHEMICAL CO., LTD
To: SK GEO CENTRIC CO., LTD.
Reel/Frame 061371/0332 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 20, 2019
From: SUJITH, SUDEVAN; SIM, SO HEE; PARK, HYO SEUNG; KIM, SUN YOUNG; LEE, SANG ICK; LEE, HAN SOL
To: SK INNOVATION CO., LTD.; SK GLOBAL CHEMICAL CO., LTD.
Reel/Frame 048643/0820 →
Priority Claims (2)
KR 10-2016-0089159 · Jul 14, 2016 · national
KR 10-2017-0062436 · May 19, 2017 · national
Continuity (1)
Related Publication 20190284109A1 · Sep 19, 2019