Heat management in ethylene oligomerization

Patent metadata

Field	Value
Publication number	US-10160696-B2
Application number	US-201615136015-A
Country	US
Kind code	B2
Filing date	Apr 22, 2016
Priority date	Dec 1, 2010
Publication date	Dec 25, 2018
Grant date	Dec 25, 2018

Abstract

The oligomerization of ethylene using a chromium catalyst having a heteroatomic ligand may be used to provide oligomerization products that are selective towards hexene and/or octene. However, such processes also typically produce some polymer as an undesirable by product. The present invention is directed towards improvements in the selective oligomerization of ethylene.

First claim

What is claimed is:

1. A method for mitigating the formation of by-product polyethylene that is produced during a selective tetramerization of ethylene, said method comprising:
a) providing a reactor system comprising at least one reactor, wherein said reactor system comprises:
1) a first heat exchanger that is used to provide heat to said reactor system; and
2) a second heat exchanger that is used to remove heat from said reactor system;

b) contacting ethylene, a solvent, and hydrogen prior to being introduced into said at least one reactor; and
c) contacting, in said at least one reactor, said ethylene, solvent, and hydrogen with:
i) a catalyst comprising:
1.1) a source of chromium that is soluble in said solvent; and
1.2) a ligand defined by the formula (R 1 )(R 2 )—P 1 -bridge-P 2 (R 3 )(R 4 ),
wherein R 1 , R 2 , R 3 , and R 4 are independently selected from the group consisting of an unsubstituted phenyl group and a phenyl group having only a single ortho-fluoro-substituent;
wherein said bridge is bonded to both phosphorus atoms and defined by the formula —N(R 5 )—; and
wherein R 5 is selected from the group consisting of hydrogen, an alkyl group, a substituted alkyl group, an aryl group, a substituted aryl group, an aryloxy group, a substituted aryloxy group, a halogen, an alkoxycarbonyl group, a carbonyloxy group, an alkoxy group, an aminocarbonyl group, a dialkylamino group, and a silyl group, and

ii) an activator comprising an aluminoxane;

d) selectively tetramerizing the ethylene at a temperature of from 10° C. to 100° C. and at a pressure of from 5 to 100 atmospheres in the at least one reactor

to produce a liquid product comprising octene and hexene, wherein:
(i) the weight ratio of octene to hexene is greater than 2:1; and
(ii) less than 5 weight % of the octene contains internal olefins,
wherein the formation of by-product polyethylene during said selective tetramerization of ethylene is reduced compared to the same selective tetramerization of ethylene in which only ethylene and solvent are contacted prior to being introduced into said at least one reactor and in which the ethylene and solvent are subsequently contacted with hydrogen in said at least one reactor.

2. The method of claim 1 , wherein said at least one reactor comprises a liquid full continuously stirred tank reactor.

3. The method of claim 1 , wherein said at least one reactor comprises a continuously stirred tank reactor and a tubular reactor downstream of the continuously stirred tank reactor,
wherein said contacting said ethylene, solvent, and hydrogen, with said catalyst and activator in said at least one reactor comprises contacting said ethylene, solvent, and hydrogen, with said catalyst and activator in said continuously stirred tank reactor; and
wherein said selectively tetramerizing the ethylene in said at least one reactor comprises:
(a) selectively tetramerizing the ethylene at a temperature of from 10° C. to 100° C. and at a pressure of from 5 to 100 atmospheres in the continuously stirred tank reactor to produce a first tetramerization product;
(b) passing said first tetramerization product from said continuously stirred tank reactor to said tubular reactor along with fresh feed comprising ethylene and solvent, wherein said fresh feed is colder than said first tetramerization product; and
(c) converting both said ethylene in the fresh feed and said first tetramerization product in the tubular reactor to said liquid product comprising octene and hexene.

4. The method of claim 3 , further characterized in that said first tetramerization product is initially cooled in a heat exchanger prior to being fed to said tubular reactor.

5. The method of claim 1 , wherein said at least one reactor comprises a first continuously stirred tank reactor having a first reactor volume and a second continuously stirred tank reactor having a second reactor volume,
wherein the second continuously stirred tank reactor is downstream of the first continuously stirred tank reactor,
wherein the second reactor volume is greater than the first reactor volume,
wherein said contacting said ethylene, solvent, and hydrogen, with said catalyst and activator in said at least one reactor comprises contacting said ethylene, solvent, and hydrogen, with said catalyst and activator in said first continuously stirred tank reactor; and
wherein said selectively tetramerizing the ethylene in said at least one reactor comprises:
a) selectively tetramerizing the ethylene at a temperature of from 10° C. to 100° C. and at a pressure of from 5 to 100 atmospheres in the first continuously stirred tank reactor to produce a first tetramerizion product;
b) passing said first tetramerization product from said first continuously stirred tank reactor to said second continuously stirred tank reactor along with fresh feed comprising ethylene and solvent; and
c) converting both said ethylene in the fresh feed and said first tetramerization product in the second continuously stirred tank reactor to said liquid product comprising octene and hexene.

6. The method of claim 2 , wherein liquid full continuously stirred tank reactor is characterized by having an agitator shaft, wherein said agitator shaft comprises an agitator shaft seal that contains a fluid channel contained therein that permits fluid flushing of said agitator shaft.

7. The method of claim 1 , further characterized in that a portion of said ethylene is dissolvent in said solvent in a solution absorber that is external to said reactor system, wherein said solution absorber is equipped with a third heat exchanger for removal of heat of absorption.

8. A method for mitigating the formation of by-product polyethylene that is produced during a selective tetramerization of ethylene, said method comprising:
a) providing a reactor system comprising at least one reactor, wherein said reactor system comprises:
1) a first heat exchanger that is used to provide heat to said reactor system; and
2) a second heat exchanger that is used to remove heat from said reactor system;

b) contacting ethylene, a solvent, and hydrogen prior to being introduced into said at least one reactor; and
c) contacting, in said at least one reactor, said ethylene, solvent, and hydrogen with:
i) a catalyst comprising:
1.1) a source of chromium that is soluble in said solvent; and
1.2) a ligand defined by the formula (R 1 )(R 2 )—P 1 -bridge-P 2 (R 3 )(R 4 ),
wherein R 1 , R 2 , R 3 , and R 4 are independently selected from the group consisting of an unsubstituted phenyl group and a phenyl group having only a single ortho-fluoro-substituent, wherein at least one of R 1 , R 2 , R 3 , and R 4 is a phenyl group having a single ortho-fluoro-substituent;
wherein said bridge is bonded to both phosphorus atoms and defined by the formula —N(R 5 )—; and
wherein R 5 is selected from the group consisting of hydrogen, an alkyl group, a substituted alkyl group, an aryl group, a substituted aryl group, an aryloxy group, a substituted aryloxy group, a halogen, an alkoxycarbonyl group, a carbonyloxy group, an alkoxy group, an aminocarbonyl group, a dialkylamino group, and a silyl groups, group, and

ii) an activator comprising an aluminoxane;

d) selectively tetramerizing the ethylene at a temperature of from 10° C. to 100° C. and at a pressure of from 5 to 100 atmospheres in the at least one reactor

provides to produce a liquid product comprising octene and hexene, wherein:
(i) the weight ratio of octene to hexene is greater than 2:1; and
(ii) less than 5 weight % of the octene contains internal olefins,
wherein the formation of by-product polyethylene during said selective tetramerization of ethylene is reduced compared to the same sel

Assignees

• Nova Chem Int Sa

Inventors

• Jaber Isam
• Jobe Ian Ronald
• Chisholm P Scott
• Krzywicki Andrzej
• Carter Charles Ashton Garret
• Strom Vernon Lindsay
• Serhal Kamal Elias
• Clavelle Eric
• Brown Stephen John
• Lacombe Yves
• Magis Anita Sylvia
• Harris Mackenzie Alexander
• Archer Russell Kirk
• Besenski Keith Wayne
• Berghmans Michel
• Golovchenko Oleksiy
• Sieben Dale Alexander

Classifications

• C07C2/36 Primary

  as phosphines, arsines, stilbines or bismuthines · CPC title

• C07C2523/26

  Chromium · CPC title

• C07C11/02

  Alkenes · CPC title

• C07C2531/14

  of aluminium or boron · CPC title

• C07C11/107

  with six carbon atoms · CPC title