Regeneration of carbenium pseudo ionic liquids

Patent metadata

Field	Value
Publication number	US-2016288044-A1
Application number	US-201514675237-A
Country	US
Kind code	A1
Filing date	Mar 31, 2015
Priority date	Mar 31, 2015
Publication date	Oct 6, 2016
Grant date	—

Abstract

A method for regenerating sulfur rich carbenium pseudo ionic liquid is described. The method includes contacting the sulfur rich carbenium pseudo ionic liquid containing at least one sulfur compound with at least one silane compound in a regeneration zone under regeneration conditions. The carbenium pseudo ionic liquid comprises an organohalide and a metal halide. The silane compound reacts to form a silyl compound, resulting in a carbenium pseudo ionic liquid phase and an organic phase containing the sulfur and the silyl compound.

First claim

What is claimed is:

1 . A method for regenerating sulfur rich carbenium pseudo ionic liquid comprising:
contacting the sulfur rich carbenium pseudo ionic liquid containing at least one sulfur compound with at least one silane compound in a regeneration zone under regeneration conditions, the carbenium pseudo ionic liquid comprising an organohalide and a metal halide, the at least one silane compound forming at least one silyl compound, resulting in a carbenium pseudo ionic liquid phase and an organic phase containing the sulfur and the at least one silyl compound.

2 . The method of claim 1 further comprising:
mixing an acid or an acid precursor with the carbenium pseudo ionic liquid phase to reactivate the carbenium pseudo ionic liquid; and
recycling the reactivated carbenium pseudo ionic liquid to a contaminant removal zone.

3 . The method of claim 2 further comprising separating the carbenium pseudo ionic liquid phase from the organic phase before mixing the acid or the acid precursor with the carbenium pseudo ionic liquid phase.

4 . The method of claim 1 further comprising:
reacting the at least one silyl compound to regenerate the at least one silane compound.

5 . The method of claim 4 further comprising separating the at least one regenerated silane compound from the organic phase.

6 . The method of claim 4 further comprising:
separating the at last one silyl compound from the organic phase before reacting the at least one silyl compound to regenerate the at least one silane compound.

7 . The method of claim 1 wherein contacting the sulfur rich carbenium pseudo ionic liquid with the at least one silane compound comprises contacting the sulfur rich carbenium pseudo ionic liquid with the at least one silane compound and a solvent, wherein the solvent is capable of forming a separate phase from the carbenium pseudo ionic liquid.

8 . The method of claim 7 further comprising:
reacting the at least one silyl compound to regenerate the at least one silane compound; and
separating the at least one regenerated silane compound from the solvent.

9 . The method of claim 7 wherein a volume ratio of the solvent to the sulfur rich carbenium pseudo ionic liquid is in a range of about 1:100 to about 100:1.

10 . The method of claim 9 wherein the solvent comprises a normal paraffin, an isoparaffin, or a cyclic paraffin having up to 10 carbon atoms, an aromatic, or the at least one silane compound.

11 . The method of claim 1 wherein a molar ratio of the at least one silane compound to the metal in the carbenium pseudo ionic liquid is in a range of about 1:100 to about 100:1.

12 . The method of claim 11 wherein the regeneration conditions include at least one of: a temperature in a range of from about −20° C. to less than a decomposition temperature of the carbenium pseudo ionic liquid, and a contacting time of about 5 sec to about 2 hr.

13 . The method of claim 11 further comprising pretreating the sulfur rich carbenium pseudo ionic liquid before contacting the sulfur rich carbenium pseudo ionic liquid with the at least one silane compound.

14 . The method of claim 1 wherein contacting the sulfur rich carbenium pseudo ionic liquid with the at least one silane compound further comprises mixing the sulfur rich carbenium pseudo ionic liquid with the at least one silane compound.

15 . The method of claim 1 wherein the at least one silane compound has a formula: R 3 SiH, R 2 SiH 2 , RSiH 3 , or SiH 4 , where each R is independently selected from hydrocarbons or halides.

16 . The method of claim 1 wherein the sulfur rich carbenium pseudo ionic liquid comprises a combination of the carbenium pseudo ionic liquid and an ionic liquid.

17 . A method for regenerating the sulfur rich carbenium pseudo ionic liquid comprising:
contacting the sulfur rich carbenium pseudo ionic liquid containing at least one sulfur compound with at least one silane compound in a regeneration zone under regeneration conditions, the carbenium pseudo ionic liquid comprising an organohalide and a metal halide, the at least one silane compound forming at least one silyl compound, resulting in a carbenium pseudo ionic liquid phase and an organic phase containing the sulfur and the at least one silyl compound; separating the carbenium pseudo ionic liquid phase from the organic phase; mixing an acid or an acid precursor with the separated carbenium pseudo ionic liquid phase to reactivate the carbenium pseudo ionic liquid; and reacting the at least one silyl compound with a metal hydride to regenerate the at least one silane compound.

18 . The method of claim 17 wherein contacting the sulfur rich carbenium pseudo ionic liquid with the at least one silane compound comprises contacting the sulfur rich carbenium pseudo ionic liquid with the at least one silane compound and a solvent, wherein the solvent is capable of forming a separate phase from the carbenium pseudo ionic liquid.

19 . The method of claim 18 wherein a volume ratio of the solvent to the sulfur rich carbenium pseudo ionic liquid is in a range of about 1:100 to about 100:1, or wherein a molar ratio of the at least one silane compound to the metal in the carbenium pseudo ionic liquid is in a range of about 1:100 to about 100:1, or both.

20 . The method of claim 17 wherein the at least one silane compound has a formula: R 3 SiH, R 2 SiH 2 , RSiH 3 , or SiH 4 , where each R is independently selected from hydrocarbons or halides.

Assignees

• Uop Llc

Inventors

• Broderick Erin M
• Bhattacharyya Alakananda

Classifications

• C07F9/5407

  Acyclic saturated phosphonium compounds · CPC title

• B01D2252/30

  Ionic liquids and zwitter-ions · CPC title

• C07C309/30

  of six-membered aromatic rings substituted by alkyl groups · CPC title

• B01D53/1425 Primary

  Regeneration of liquid absorbents · CPC title

• B01D53/1493

  Selection of liquid materials for use as absorbents · CPC title