Process for oligomerization of ethylene

Patent metadata

Field	Value
Publication number	US-10112876-B2
Application number	US-201314125805-A
Country	US
Kind code	B2
Filing date	Sep 5, 2013
Priority date	Nov 28, 2012
Publication date	Oct 30, 2018
Grant date	Oct 30, 2018

Abstract

The present invention relates to a process for the oligomerization of ethylene, comprising: a) oligomerization of ethylene in a reactor in the presence of solvent and catalyst; b) transferring reactor overhead effluent to an externally located cooling device and recycling condensed effluent into the reactor; c) transferring the reactor bottom effluent to a series of fractionation columns and, in the following order, i) optionally separating a C4 fraction, ii) separating a C6 fraction, iii) simultaneously separating C8 and C10 fractions and recycling thereof into the reactor , and iv) separating residues comprising ≥C12 fractions, spent catalyst polymer material and quench media, from the process, wherein the solvent is separated in any of the steps i)-iv)and/or in an additional step.

First claim

The invention claimed is:

1. A process for oligomerizing ethylene, comprising:
a) oligomerizing ethylene in a reactor in the presence of a solvent and a catalyst;
b) transferring a reactor overhead effluent from the reactor to an externally located cooling device to condense a portion of the reactor overhead effluent and recycling the condensed portion of the reactor overhead effluent into the reactor;
c) recovering a reactor bottom effluent from the reactor, wherein the reactor bottom effluent comprises C4 hydrocarbons, C6 hydrocarbons, C8 hydrocarbons, C10 hydrocarbons, residual C12+ hydrocarbons, residual spent catalyst, and residual polymer material;
d) transferring the reactor bottom effluent to a quenching unit, wherein quench media is added to the reactor bottom effluent, to produce a quenched reactor bottom effluent;
e) transferring the quenched reactor bottom effluent to a series of fractionation columns and, in the following order,
i) optionally separating a fraction comprising the C4 hydrocarbons from the quenched reactor bottom effluent;
ii) separating a fraction comprising the C6 hydrocarbons from the quenched reactor bottom effluent;
iii) separating a fraction comprising both the C8 hydrocarbons and C10 hydrocarbons from the quenched reactor bottom effluent and recycling said fraction comprising both the C8 hydrocarbons and C10 hydrocarbons into the reactor, and
iv) separating the residual C12+ hydrocarbons, the residual spent catalyst, the residual polymer material, and residual quench media from the quenched reactor bottom effluent,

wherein the solvent is separated from the quenched reactor bottom effluent in any of steps i)-iv) and/or in an additional step.

2. The process according to claim 1 , wherein the catalyst comprise (1) a chromium compound,(2) a lingand of the general structure (A) R 1 R 2 P—N(R 3 )—P(R 4 )—N(R 5 )—H or (B) R 1 R 2 P—N(R 3 )—P(R 4 )—N(R 5 )—PR 6 R 7 , wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are independently selected from halogen groups, amino groups, a trimethylsilyl group, C 1 -C 10 alkyl groups, C 6 -C 20 aryl groups, and substituted C 6 -C 20 aryl groups, and (3) an activator or co-catalyst.

3. The process according to claim 2 , wherein the chromium compound is selected from the group consisting of CrCl 3 (THF) 3 , Cr(III) acetyl acetonate, Cr(III) octanoate, chromium hexacarbonyl, Cr(III)-2-ethyl hexanoate, benzene(tricarbonyl)-chormium, and Cr(III) chloride.

4. The process according to claim 2 , wherein the activator or co-catalyst is selected from trimethyl aluminum, triethyl aluminum, triisopropyl aluminum, triisobutyl aluminum, ethylaluminum sesquichloride, diethyl aluminum chloride, ethyl aluminum dichloride, methyl aluminoxane (MAO) or mixtures thereof.

5. The process according to claim 1 , wherein oligomerizing ethylene comprises trimerizing ethylene.

6. The process according to claim 1 , wherein the condensed portion of the reactor overhead effluent recycled to the reactor comprises unreacted ethylene.

7. The process according to claim 1 , wherein the condensed portion of the reactor overhead effluent is at a temperature of −30° C. to +10° C. prior to being recycled into the reactor.

8. The process according to claim 1 , wherein make-up ethylene is added to the condensed portion of the reactor overhead effluent to be recycled into the reactor.

9. The process according to claim 1 , wherein the fraction comprising both the C8 hydrocarbons and C10 hydrocarbons obtained in step iii) is recycled into the reactor at a temperature of about 10-20° C.

10. The process according to claim 1 , wherein the content of C4 hydrocarbons in the reactor is from 5 to 30 weight percent, the content of C8 hydrocarbons in the reactor is from 1 to 2 weight percent, and/or the content of C10 hydrocarbons in the reactor is from 5 to 30 weight percent, where all weight percentages are based on the total weight of liquids contained in the reactor.

11. The process according to claim 1 , wherein the total content of linear alpha-olefins in the reactor is from 30 to 75 weight percent based on the total weight of liquids contained in the reactor.

12. The process according to claim 1 , wherein the reactor is a multi tubular reactor and/or a bubble column reactor.

Assignees

• Saudi Basic Ind Corp
• Linde Ag

Inventors

• Azam Shahid Majeed
• Iliyas Abduljelil
• Alqahtani Abdullah Mohammad
• Khurram Shehzada
• Wöhl Anina
• Müller Wolfgang
• Harff Marco
• Meiswinkel Andreas
• Bölt Heinz

Classifications

• C07C11/107

  with six carbon atoms · CPC title

• C07C2531/34

  of chromium, molybdenum or tungsten · CPC title

• C07C2/36 Primary

  as phosphines, arsines, stilbines or bismuthines · CPC title

• C07C2531/20

  Carbonyls · CPC title

• C07C2531/22

  Organic complexes · CPC title