Contaminant removal from hydrocarbon streams with lewis acidic ionic liquids

Patent metadata

Field	Value
Publication number	US-9574139-B2
Application number	US-201414552345-A
Country	US
Kind code	B2
Filing date	Nov 24, 2014
Priority date	Nov 24, 2014
Publication date	Feb 21, 2017
Grant date	Feb 21, 2017

Abstract

Processes for removing sulfur and nitrogen contaminants from hydrocarbon streams are described. The processes include contacting the hydrocarbon stream comprising the contaminant with lean halometallate ionic liquid an organohalide resulting in a mixture comprising the hydrocarbon and rich halometallate ionic liquid comprising the contaminant. The mixture is separated to produce a hydrocarbon effluent and a rich halometallate ionic liquid effluent comprising the rich halometallate ionic liquid comprising the contaminant.

First claim

What is claimed is:

1. A process for removing a contaminant comprising at least one of sulfur and nitrogen from a hydrocarbon stream comprising:
contacting the hydrocarbon stream comprising the contaminant with a lean hydrocarbon-immiscible halometallate ionic liquid and an organohalide or HCl resulting in a mixture comprising the hydrocarbon and a rich hydrocarbon-immiscible halometallate ionic liquid comprising the contaminant wherein the hydrocarbon-immiscible halometallate ionic liquid comprises a haloaluminate ionic liquid, a haloferrate ionic liquid, a halocuprate ionic liquid, a halozincate ionic liquid, or combinations thereof and wherein the aloaluminate in said haloaluminate ionic liquid is selected from the group consisting of Al 2 Cl 7 − , Al 3 Cl 10 − , Al 2 Cl 6 Br, Al 3 Cl 9 Br, Al 2 Br 7 − , and Al 3 Br 10 ; and
separating the mixture to produce a hydrocarbon effluent and a rich hydrocarbon-immiscible halometallate ionic liquid effluent comprising the rich hydrocarbon-immiscible halometallate ionic liquid comprising the contaminant.

2. The process of claim 1 wherein the hydrocarbon-immiscible halometallate ionic liquid comprises at least one of nitrogen containing ionic liquids and phosphorus containing ionic liquids.

3. The process of claim 1 wherein the hydrocarbon-immiscible halometallate ionic liquid comprises an imidazolium ionic liquid, an ammonium ionic liquid, a pyridinium ionic liquid, a phosphonium ionic liquid, a pyrrolidinium ionic liquid, a lactamium ionic liquid, or combinations thereof.

4. The process of claim 1 wherein the organohalide comprises an alkyl halide, an isoalkyl halide, a cycloalkyl halide, or combinations thereof.

5. The process of claim 1 wherein the organohalide comprises tert-butyl chloride, tert-butyl bromide, 2-chlorobutane, 2-bromobutane, cyclopentyl chloride, cyclopentyl bromide, butyl chloride, butyl bromide, propyl chloride, propyl bromide, or combinations thereof.

6. The process of claim 1 where the organohalide is present in an amount between about 1 wt % and about 50 wt % of an amount of ionic liquid.

7. The process of claim 1 wherein the organohalide has 1-12 carbon atoms.

8. The process of claim 1 wherein the hydrocarbon stream has a boiling point in a range of about 30° C. to about 610° C.

9. The process of claim 1 wherein the contacting step is conducted under at least one of: a temperature in a range of about −20° C. to about 100° C., a pressure in a range of about 0.1 MPa to about 3 MPa, and an inert atmosphere.

10. The process of claim 1 further comprising passing at least a portion of the hydrocarbon effluent to a hydrocarbon conversion zone.

11. The process of claim 1 wherein a weight ratio of the hydrocarbon stream to the hydrocarbon-immiscible halometallate ionic liquid and the organohalide is in a range of about 1:1,000 to about 1,000:1.

12. A process for removing a contaminant comprising at least one of sulfur and nitrogen from a hydrocarbon stream comprising:
contacting the hydrocarbon stream comprising the contaminant with a lean hydrocarbon-immiscible halometallate ionic liquid and an organohalide or HCl resulting in a mixture comprising the hydrocarbon and a rich hydrocarbon-immiscible halometallate ionic liquid comprising the contaminant, wherein the hydrocarbon-immiscible halometallate ionic liquid comprises an imidazolium ionic liquid, an ammonium ionic liquid, a pyridinium ionic liquid, a phosphonium ionic liquid, a pyrrolidinium ionic liquid, a lactamium ionic liquid, or combinations thereof, and wherein the organohalide comprises an alkyl halide, an isoalkyl halide, a cycloalkyl halide, or combinations thereof; and
separating the mixture to produce a hydrocarbon effluent and a rich hydrocarbon-immiscible halometallate ionic liquid effluent comprising the rich hydrocarbon-immiscible halometallate ionic liquid comprising the contaminant; wherein the hydrocarbon-immiscible halometallate ionic liquid comprises a haloaluminate ionic liquid, a haloferrate ionic liquid, a halocuprate ionic liquid, a halozincate ionic liquid, or combinations thereof and wherein the aloaluminate in said haloaluminate ionic liquid is selected from the group consisting of Al 2 Cl 7 − , Al 3 Cl 10 − , Al 2 Cl 6 Br, Al 3 Cl 9 Br, Al 2 Br 7 − , and Al 3 Br 10 .

13. The process of claim 12 wherein the organohalide comprises tert-butyl chloride, tert-butyl bromide, 2-chlorobutane, 2-bromobutane, cyclopentyl chloride, cyclopentyl bromide, butyl chloride, butyl bromide, propyl chloride, propyl bromide, or combinations thereof.

14. The process of claim 12 where the organohalide is present in an amount between 1 wt % and 50 wt % of an amount of ionic liquid.

15. The process of claim 12 wherein the hydrocarbon stream has a boiling point in a range of about 30° C. to about 610° C.

16. The process of claim 12 wherein the contacting step is conducted under at least one of a temperature in a range of about −20° C. to about 100° C., a pressure in a range of about 0.1 MPa to about 3 MPa, and an inert atmosphere.

17. The process of claim 12 wherein a ratio of the hydrocarbon stream to the hydrocarbon-immiscible halometallate ionic liquid and the organohalide is in a range of about 1:1,000 to about 1,000:1.

18. The process of claim 12 further comprising passing at least a portion of the hydrocarbon effluent to a hydrocarbon conversion zone.

Assignees

• Uop Llc

Inventors

• Broderick Erin M
• Bhattacharyya Alakananda
• Yang Shurong
• Mezza Beckay J

Classifications

• C10G67/08

  including acid treatment as the refining step in the absence of hydrogen · CPC title

• C10G55/06

  including at least one catalytic cracking step · CPC title

• C10G17/07 Primary

  using halogen acids or oxyacids of halogen (acids generating halogen C10G27/02) · CPC title

• C10G21/18

  Halogen-containing compounds · CPC title

• C10G2300/202

  Heteroatoms content, i.e. S, N, O, P · CPC title