Systems and methods incorporating ionic liquids for electrochemically mediated capturing of lewis acid gases

Patent metadata

Field	Value
Publication number	US-10286355-B2
Application number	US-201715660587-A
Country	US
Kind code	B2
Filing date	Jul 26, 2017
Priority date	Jul 27, 2016
Publication date	May 14, 2019
Grant date	May 14, 2019

Abstract

The present invention generally relates to methods and systems for capturing a Lewis acid gas (e.g., CO 2 ). In some embodiments, the methods and systems utilize an ionic liquid incorporated into one or more electrochemical cells.

First claim

What is claimed:

1. A method for capturing a Lewis acid gas, comprising:
providing a system comprising a first zone and a second zone in fluid connection with the first zone, wherein:
the first zone comprises a functional ionic liquid comprising a cation and an anion; and
the second zone comprises a complexation agent capable of associating and/or disassociating the cation to and/or from the functional ionic liquid upon exposure to an electrical potential;
exposing the ionic liquid to the Lewis acid gas in the first zone, wherein the cation associates with the Lewis acid gas to form a cation-Lewis-acid-gas complex; and
exposing the cation-Lewis-acid-gas complex to the complexation agent in the second zone,
wherein the step of exposing the cation-Lewis-acid-gas complex to the complexation agent in the second zone comprises applying an electrical potential to the complexation agent, and
wherein the complexation agent associates with the cation to form a cation-complexation agent complex and the Lewis acid gas is released to form free Lewis acid gas.

2. The method according to claim 1 , wherein the cation is represented by the following structural formula:

wherein:
R 1 has the formula: (C(R) 2 ) n , in which R is H or an optionally substituted C 1 -C 3 alkyl group; and n is 1, 2, 3, 4, 5, or 6; and
R 2 has the formula: (C(R′) 2 ) m —R″, in which R′ is H or an optionally substituted C 1 -C 3 alkyl group; R″ is H or an optionally substituted C 1 -C 3 alkyl group; and m is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

3. The method according to claim 2 , wherein n is 2.

4. The method according to claim 3 , wherein R is H.

5. The method according to claim 2 , wherein m is 6 and R″ is H.

6. The method according to claim 2 , wherein R 2 is 2-ethylhexyl.

7. The method according to claim 1 , wherein the anion of the functional ionic liquid is selected from the group consisting of boron tetrafluoride, phosphorus tetrafluoride, phosphorus hexafluoride, alkylsulfonate, fluoroalkylsulfonate, arylsulfonate, bis(alkylsulfonyl)amide, bis(fluoroalkylsulfonyl)amide, bis(arylsulfonyl)amide, (fluoroalkylsulfonyl)(fluoroalkylcarbonyl)amide, halide, nitrate, nitrite, sulfate, hydrogensulfate, alkyl sulfate, aryl sulfate, carbonate, bicarbonate, carboxylate, phosphate, hydrogen phosphate, dihydrogen phosphate, hypochlorite, and an anionic site of a cation-exchange resin.

8. The method according to claim 1 , wherein the anion of the functional ionic liquid is selected from the group consisting of boron tetrafluoride, phosphorus hexafluoride, methanesulfonate, trifluoromethanesulfonate, benzenesulfonate, p-toluenesulfonate, bis(methanesulfonyl)amide, bis(trifluoromethanesulfonyl)amide, bis(benzenesulfonyl)amide, or bis(p-toluenesulfonyl)amide.

9. The method according to claim 1 , wherein the anion of the functional ionic liquid is selected from the group consisting of methanesulfonate, trifluoromethanesulfonate, benzenesulfonate, p-toluenesulfonate, bis(methanesulfonyl)amide, bis(trifluoromethanesulfonyl)amide, bis(benzenesulfonyl)amide, or bis(p-toluenesulfonyl)amide.

10. The method according to claim 1 , wherein the anion of the functional ionic liquid is selected from the group consisting of bis(methanesulfonyl)amide, bis(trifluoromethanesulfonyl)amide, bis(benzenesulfonyl)amide, or bis(p-toluenesulfonyl)amide.

11. The method according to claim 1 , wherein the anion of the functional ionic liquid is bis(trifluoroethanesulfonyl)amide.

12. The method according to claim 1 , wherein the cation of the functional ionic liquid is dicationic or polycationic.

13. The method according to claim 1 , wherein the anion of the functional ionic liquid is dianionic or polyanionic.

14. The method according to claim 1 , wherein the Lewis acid gas is CO 2 and the cation-Lewis-acid-gas complex is a cation-CO 2 complex.

15. The method according to claim 14 , wherein the step of exposing the ionic liquid to CO 2 in the first zone comprises scrubbing a flue gas.

16. The method according to claim 1 , wherein the step of applying the electrical potential to the complexation agent comprises oxidizing an anode of an electrochemical cell.

17. The method according to claim 1 , wherein the first zone comprises a flue gas scrubbing zone.

18. The method according to claim 1 , wherein the second zone comprises an anode compartment of an electrochemical cell.

19. The method according to claim 1 , further comprising disassociating the complexation agent from the cation-complexation agent complex to restore the cation.

20. The method according to claim 1 , wherein the complexation agent comprises copper.

Assignees

• Massachusetts Inst Technology

Inventors

• Hatton Trevor Alan
• Brown Paul
• Voskian Sahag

Classifications

• B01D53/62

  Carbon oxides · CPC title

• C07C211/09

  Diamines · CPC title

• B01D2258/0283

  Flue gases · CPC title

• B01D53/326

  in electrochemical cells · CPC title

• B01D53/1425

  Regeneration of liquid absorbents · CPC title