IP Library Granted Patent US 9,956,520
Granted Patent B2
US 9,956,520 · App. 15/261,262 · Granted May 1, 2018

Liquid carbon dioxide absorbents, methods of using the same, and related systems

Inventors: Robert James Perry (Niskayuna, NY); Grigorii Lev Soloveichik (Washington, DC); Malgorzata Iwona Rubinsztajn (Ballston Spa, NY); Michael Joseph O'Brien (Niskayuna, NY); Larry Neil Lewis (Scotia, NY); Tunchiao Hubert Lam (Clifton Park, NY); Sergei Kniajanski (Clifton Park, NY); Dan Hancu (Clifton Park, NY)
Assignee: General Electric Company
B01D53/1493B01D53/1475B01D2252/202B01D2252/2025B01D2252/2026B01D2252/2028B01D2252/2041B01D2252/2056B01D2252/20415B01D2252/20421B01D2252/504F23J2215/50F23J2219/40Y02C10/06
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Quick Facts
Patent No.
US 9,956,520
App. No.
15/261,262
Granted
May 1, 2018
Kind
B2
Abstract

A carbon dioxide absorbent composition is described, including (i) a liquid, nonaqueous silicon-based material, functionalized with one or more groups that either reversibly react with CO 2 or have a high-affinity for CO 2 , and (ii) a hydroxy-containing solvent that is capable of dissolving both the silicon-based material and a reaction product of the silicon-based material and CO 2 . The absorbent may be utilized in methods to reduce carbon dioxide in an exhaust gas, and finds particular utility in power plants.

Claims (19)

1. A method for reducing the amount of carbon dioxide in a process stream comprising contacting the stream with a carbon dioxide absorbent comprising (i) a liquid, nonaqueous silicon-based material, functionalized with one or more nitrogen atom-containing groups that reversibly react with CO 2 and/or have a high-affinity for CO 2 ; and (ii) a hydroxy-containing solvent that is capable of dissolving both the silicon-based material and a reaction product of the silicon-based material and carbon dioxide.

2. The method of claim 1 , wherein the process stream comprises an exhaust stream.

3. The method of claim 1 , wherein the hydroxy-containing solvent comprises trimethylolpropane ethoxylates, glycerol, ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 1,3-bis(3-hydroxypropyl)tetramethyldisiloxane, a hydrosilylation reaction product of 1,1,3,3-tetramethyldisiloxane and trimethylolpropane allylether, or combinations of these.

4. The method of claim 1 , wherein the carbon dioxide solvent further comprises water.

5. The method of claim 1 , wherein the functionalized silicon-based material comprises one or more aminosilicones.

6. The method of claim 1 , wherein the functionalized silicon-based material comprises silanes, or compounds containing one or more siloxy units, or combinations of thereof.

7. The method of claim 1 , wherein the functional group(s) comprise(s) one or more aliphatic amines, imines, amidines, amides, heterocyclic amino compounds, aromatic amines, and combinations thereof.

8. The method of claim 1 , wherein the functional group(s) comprise(s) one or more amino hydroxy groups.

9. The method of claim 1 , wherein the solvent has a vapor pressure below about 150 mm Hg at 100° C.

10. The method of claim 1 , wherein the absorbent further comprises antioxidants, stabilizers, accelerators, antifoaming agents or blends thereof.

11. The method of claim 1 , wherein the nitrogen atom-containing functional group is not a sterically hindered amine.

12. The method of claim 1 , wherein the functionalized, silicon-based material comprises less than 20 repeating, monomeric units.

13. The method of claim 12 , wherein the functionalized, silicon-based material comprises 10 or less repeating, monomeric units.

14. The method of claim 1 , wherein the solvent comprises two or more hydroxyl groups.

15. The method of claim 14 , wherein the solvent comprises a glycol, a hydroxylated silicone, a phenol, or combinations of the foregoing.

16. The method of claim 15 , wherein the solvent comprises trimethylolpropane ethoxylates, glycerol, triethylene glycol, tetraethylene glycol, 1,3-bis(3-hydroxypropyl)tetramethyldisiloxane, a hydrosilylation reaction product of 1,1,3,3-tetramethyldisiloxane and trimethylolpropane allyl ether, eugenol, isoeugenol, 2-allyl-6-methylphenol, 2-allylphenol or combinations of the foregoing.

17. The method of claim 1 , wherein the functional group(s) comprise(s) one or more amines.

18. The method of claim 17 , wherein the functional group(s) comprise(s) one or more di-, tri- and polyamines, or combinations of the forgoing.

19. The method of claim 18 , wherein the functional group(s) comprise(s) one or more aminoethylaminopropyl piperazinopropyl, aminomethylaminoethyl, 2-aminopropylpyridyl, groups or combinations of these.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2019
From: GENERAL ELECTRIC COMPANY
To: AIR PRODUCTS AND CHEMICALS, INC.
Reel/Frame 050798/0659 →
CONFIRMATORY LICENSE Recorded Sep 19, 2017
From: GENERAL ELECTRIC GLOBAL RESEARCH
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 043630/0219 →
GOVERNMENT INTEREST AGREEMENT Recorded Sep 19, 2017
From: GENERAL ELECTRIC GLOBAL RESEARCH
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 043902/0658 →
Continuity (4)
Division 13332843 · Dec 21, 2011
Continuation In Part 12512577 · Jul 30, 2009
Continuation In Part 12343905 · Dec 24, 2008
Related Publication 20160375400A1 · Dec 29, 2016