IP Library Granted Patent US 12,611,629
Granted Patent B2
US 12,611,629 · App. 17/735,943 · Granted Apr 28, 2026

Systems and methods for capturing carbon dioxide and regenerating a capture solution

Inventors: Kyle Wayne Kemp (Coquitlam, CA); Andrew Logan Ostericher (Squamish, CA); Douglas Edward Olmstead (Squamish, CA)
Assignee: Carbon Engineering ULC
B01D53/1425B01D53/1475B01D53/78B01D61/422C25B1/20C25B1/23B01D2251/304B01D2251/306B01D2251/604B01D2257/504B01D2311/2643
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Quick Facts
Patent No.
US 12,611,629
App. No.
17/735,943
Granted
Apr 28, 2026
Kind
B2
Abstract

Techniques according to the present disclosure include capturing carbon dioxide from a dilute gas source with a CO 2 capture solution to form a carbonate-rich capture solution; separating at least a portion of carbonate from the carbonate-rich capture solution; forming an electrodialysis (ED) feed solution; flowing a water stream and the ED feed solution to a bipolar membrane electrodialysis (BPMED) unit; applying an electric potential to the BPMED unit to form at least two ED product streams including a first ED product stream including a hydroxide; and flowing the first ED product stream to use in the capturing the carbon dioxide from the dilute gas source with the CO 2 capture solution.

Claims (84)

1 . A method comprising:

capturing carbon dioxide from a dilute gas source with a CO 2 capture solution to form a carbonate-rich capture solution;

increasing a concentration of carbonate in the carbonate-rich capture solution by crystallizing the carbonate-rich capture solution to form a mother liquor and a crystalline carbonate hydrate;

forming an electrodialysis (ED) feed solution;

flowing a water stream and the ED feed solution to a bipolar membrane electrodialysis (BPMED) unit;

applying an electric potential to the BPMED unit to form at least two ED product streams including a first ED product stream that includes a hydroxide; and

flowing the first ED product stream to use in capturing the carbon dioxide from the dilute gas source with the CO 2 capture solution.

2 . The method of claim 1 , wherein applying the electric potential to the BPMED unit includes applying at least a portion of the electric potential to the BPMED unit to form the first ED product stream and a second ED product stream.

3 . The method of claim 2 , wherein the second ED product stream includes carbonic acid, the method further comprising recovering at least a portion of a carbon dioxide gas stream from the second ED product stream.

4 . The method of claim 3 , wherein recovering the portion of the carbon dioxide gas stream from the second ED product stream includes recovering at least the portion of the carbon dioxide gas stream from the second ED product stream to form a brine stream, the method comprising:

dissolving the crystalline carbonate hydrate and mixing the dissolved crystalline carbonate hydrate with the brine stream to form the ED feed solution before flowing the water and the ED feed solution to the BPMED unit.

5 . The method of claim 4 , wherein recovering the portion of the carbon dioxide gas stream from the second ED product stream to form the brine stream includes recovering the portion of the carbon dioxide gas stream in a flash tank, the method further comprising:

flowing the brine stream from the flash tank to use in the dissolving the crystalline carbonate hydrate and mixing the dissolved crystalline carbonate hydrate with the brine stream to form the ED feed solution.

6 . The method of claim 4 , comprising:

flowing the carbon dioxide gas stream to a downstream process comprising at least one of: a compression unit, a fuel synthesis system, a syngas generation reactor, or an electrolyzer cell; and

yielding one or more downstream products comprising at least one of: syngas, CO, H 2 , or water.

7 . The method of claim 2 , wherein the second ED product stream includes a proton-shuttling species, the method further comprising:

reacting the second ED product stream with the portion of carbonate to recover the carbon dioxide gas and to form the ED feed solution.

8 . The method of claim 7 , wherein reacting the second ED product stream with the portion of carbonate to recover the carbon dioxide gas includes reacting the proton-shuttling species of the second ED product stream with the portion of carbonate to form carbonic acid and the ED feed solution.

9 . The method of claim 7 , comprising:

flowing the carbon dioxide gas to a downstream process comprising at least one of: a compression unit, a fuel synthesis system, a syngas generation reactor, or an electrolyzer cell; and

yielding one or more downstream products comprising at least one of: syngas, CO, H 2 , or water.

10 . The method of claim 7 , wherein reacting the second ED product stream with the portion of carbonate includes reacting the proton-shuttling species comprising bisulfate with the portion of carbonate.

11 . The method of claim 1 , comprising flowing the ED feed solution through an ion exchanger before flowing the water and the ED feed solution to the BPMED unit.

12 . The method of claim 1 , comprising separating a BPMED recycle stream from the first ED product stream, and returning the BPMED recycle stream to the BPMED unit.

13 . The method of claim 2 , comprising:

flowing the carbonate-rich capture solution through a nanofiltration unit to form a nanofiltration (NF) retentate stream comprising a carbonate-rich mixture, and to form a NF permeate stream comprising a hydroxide-rich mixture, and flowing the water and the ED feed solution to the BPMED unit includes flowing the ED feed solution comprising at least a portion of the NF retentate stream to the BPMED unit, the method further comprising:

recovering a carbon dioxide gas from the second ED product stream to form a brine stream;

flowing the brine stream to a reverse osmosis (RO) unit to form an RO retentate stream comprising a bicarbonate-rich solution and to form an RO permeate stream comprising water; and

combining the RO retentate stream with the NF retentate stream to form the ED feed solution.

14 . The method of claim 13 , comprising flowing at least a portion of the NF permeate stream to use in the capturing the carbon dioxide from the dilute gas source with the CO 2 capture solution.

15 . The method of claim 13 , comprising flowing the NF retentate stream to an ion exchanger downstream of the nanofiltration unit to form an ion exchange regenerate waste stream and at least a portion of the ED feed solution.

16 . The method of claim 13 , comprising combining at least a portion of the RO permeate stream comprising water with the first ED product stream to form a BPMED recycle stream.

17 . The method of claim 1 , comprising increasing a concentration of hydroxide in the first ED product stream to form the CO 2 capture solution before capturing the carbon dioxide from the dilute gas source with the CO 2 capture solution.

18 . The method of claim 1 , comprising:

dissolving at least a portion of the crystalline carbonate hydrate to form a portion of carbonate; and

mixing the portion of carbonate with a brine stream to form the ED feed solution.

19 . The method of claim 2 , comprising;

dissolving at least a portion of the crystalline carbonate hydrate to form a portion of carbonate; and

reacting the portion of carbonate with a proton-shuttling species in the second ED product stream to form the ED feed solution.

20 . The method of claim 1 , comprising evaporating water from the carbonate-rich capture solution to increase a concentration of carbonate before crystallizing the carbonate-rich capture solution.

21 . The method of claim 1 , comprising combining at least a portion of the mother liquor with at least a portion of the CO 2 capture solution for use in the capturing the carbon dioxide from the dilute gas source with the CO 2 capture solution.

22 . The method of claim 1 , wherein increasing the concentration of carbonate in the carbonate-rich capture solution comprises crystallizing the carbonate-rich capture solution to form a low solids stream and a high solids stream comprising the crystalline carbonate hydrate, the low solids stream having a higher liquid-to-solid ratio than the high solids stream, the method further comprising:

dissolving the crystalline carbonate hydrate of the high solids stream in an aqueous solution and mixing with a brine stream to form the ED feed solution; and

returning the low solids stream to use in the crystallizing of the carbonate-rich capture solution.

23 . A method comprising:

capturing carbon dioxide from air with a CO 2 capture solution to form a carbonate-rich capture solution;

separating at least a portion of carbonate from the carbonate-rich capture solution;

reacting a proton-shuttling species with the portion of carbonate to recover carbon dioxide gas from the portion of carbonate and to form a feed solution;

flowing a water stream and the feed solution to an electrochemical cell;

applying an electric potential to the electrochemical cell to form a first product stream that includes a hydroxide and a second product stream comprising the proton-shuttling species;

flowing the second product stream comprising the proton-shuttling species to react the proton-shuttling species with the portion of carbonate; and

flowing the first product stream to use in capturing the carbon dioxide from the air with the CO2 capture solution.

24 . The method of claim 23 , wherein:

reacting the proton-shuttling species with the portion of carbonate comprises reacting the proton-shuttling species with the portion of carbonate to form carbonic acid and the feed solution; and

degassing the carbon dioxide gas from the carbonic acid.

25 . The method of claim 24 , wherein reacting the proton-shuttling species with the portion of carbonate comprises reacting the proton-shuttling species comprising at least one of sulfuric acid and bisulfate with the portion of carbonate to form the carbonic acid and the feed solution.

26 . The method of claim 23 , wherein separating the portion of carbonate from the carbonate-rich capture solution comprises crystallizing the portion of carbonate to form a crystalline carbonate hydrate.

27 . The method of claim 26 , wherein reacting the proton-shuttling species with the portion of carbonate comprises:

dissolving the crystalline carbonate hydrate to form a dissolved inorganic carbon; and

reacting the dissolved inorganic carbon with the proton-shuttling species to form the feed solution and carbon dioxide gas, before the flowing the water stream and the feed solution to the electrochemical cell.

28 . The method of claim 26 , wherein reacting the proton-shuttling species with the portion of carbonate comprises:

dissolving the crystalline carbonate hydrate to form a dissolved inorganic carbon;

flowing the dissolved inorganic carbon to a flash tank; and

reacting the dissolved inorganic carbon with the proton-shuttling species in the flash tank to form the feed solution and carbon dioxide gas, before the flowing the water stream and the feed solution to the electrochemical cell.

29 . The method of claim 23 , wherein flowing the water stream and the feed solution to the electrochemical cell comprises:

separating a recycle stream including hydroxide from the first product stream; and

flowing the recycle stream to the electrochemical cell.

30 . The method of claim 23 , wherein flowing the water stream and the feed solution to the electrochemical cell comprises:

flowing the water to an alkaline regeneration compartment of the electrochemical cell, the alkaline regeneration compartment defined between a cathode and a cation exchange membrane of the electrochemical cell; and

flowing the feed solution to a feed compartment of the electrochemical cell separate from the alkaline regeneration compartment.

31 . The method of claim 30 , wherein flowing the feed solution to the feed compartment comprises flowing the feed solution to the feed compartment defined between an anode of the electrochemical cell and the cation exchange membrane.

32 . The method of claim 30 , wherein:

flowing the feed solution to the feed compartment comprises flowing the feed solution to the feed compartment defined between an anion exchange membrane of the electrochemical cell and the cation exchange membrane; and

applying the electric potential to the electrochemical cell comprises moving the proton-shuttling species across the anion exchange membrane into an acid compartment defined between the anion exchange membrane and an anode of the electrochemical cell.

33 . The method of claim 30 , wherein flowing the first product stream to use in capturing the carbon dioxide from the air comprises flowing the first product stream from the alkaline regeneration compartment of the electrochemical cell.

34 . The method of claim 23 , wherein flowing the first product stream to use in capturing the carbon dioxide from the air comprises:

separating the first product stream into a hydrogen stream and into the CO2 capture solution; and

flowing the CO2 capture solution to use in capturing the carbon dioxide from the air.

35 . The method of claim 23 , wherein flowing the second product stream comprising the proton-shuttling species to react the proton-shuttling species with the portion of carbonate comprises:

separating the second product stream into an oxygen stream and into a proton-shuttling species stream; and

flowing the proton-shuttling species stream to react the proton-shuttling species with the portion of carbonate.

36 . The method of claim 26 , wherein crystallizing the portion of the carbonate comprises crystallizing the portion of carbonate to form a mother liquor, the method comprising:

combining at least a portion of the mother liquor with at least a portion of the CO 2 capture solution for use in the capturing of carbon dioxide from the air with the CO 2 capture solution.

Assignments (3)
CHANGE OF NAME Recorded Feb 28, 2024
From: CARBON ENGINEERING LTD.
To: CARBON ENGINEERING ULC
Reel/Frame 066593/0551 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2022
From: BASTIDAS, TERESA JULIET PENA
To: CARBON ENGINEERING LTD.
Reel/Frame 061677/0488 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2022
From: KEMP, KYLE WAYNE; OSTERICHER, ANDREW LOGAN; OLMSTEAD, DOUGLAS EDWARD
To: CARBON ENGINEERING LTD.
Reel/Frame 059877/0866 →
Continuity (2)
Provisional Application 63183533 · May 3, 2021
Related Publication 20220362707A1 · Nov 17, 2022
References Cited (105)
US 7604724B2 · Mortson · 2009 [cited by applicant]
US 8088197B2 · Wright et al. · 2012 [cited by applicant]
US 8119091B2 · Keith et al. · 2012 [cited by applicant]
US 8357270B2 · Gilliam et al. · 2013 [cited by applicant]
US 8535502B2 · Littau et al. · 2013 [cited by applicant]
US 8679312B2 · Inoue et al. · 2014 [cited by applicant]
US 8679314B1 · Seth et al. · 2014 [cited by applicant]
US 8894830B2 · Gilliam et al. · 2014 [cited by applicant]
US 9493881B2 · Kosmoski et al. · 2016 [cited by applicant]
US 10941046B2 · Mack et al. · 2021 [cited by applicant]
US 10981114B2 · Torres et al. · 2021 [cited by applicant]
US 11219860B1 · Jakobsen · 2022 [cited by applicant]
US 11577202B2 · Demeter · 2023 [cited by applicant]
US 11857914B2 · Omosebi et al. · 2024 [cited by applicant]
US 12006580B2 · Berlinguette et al. · 2024 [cited by applicant]
US 12030016B2 · Cohen-Cole et al. · 2024 [cited by applicant]
US 12083478B2 · Lackner · 2024 [cited by applicant]
US 12115498B2 · Gobaille-Shaw et al. · 2024 [cited by applicant]
US 12187629B2 · Mustafa et al. · 2025 [cited by applicant]
US 12274977B1 · Scherpbier et al. · 2025 [cited by applicant]
US 12331414B2 · Zhang et al. · 2025 [cited by applicant]
US 20070187247A1 · Lackner et al. · 2007 [cited by applicant]
US 20100051859A1 · House et al. · 2010 [cited by applicant]
US 20100059377A1 · Littau · 2010 [cited by examiner]
US 20150083607A1 · Gilliam et al. · 2015 [cited by applicant]
US 20200317512A1 · Davis et al. · 2020 [cited by applicant]
US 20210001270A1 · Lu et al. · 2021 [cited by applicant]
US 20210371282A1 · Ning et al. · 2021 [cited by applicant]
US 20220170166A1 · Li et al. · 2022 [cited by applicant]
US 20230249133A1 · Oloman · 2023 [cited by applicant]
US 20230294043A1 · Makaruk et al. · 2023 [cited by applicant]
US 20230390702A1 · Jakobsen · 2023 [cited by applicant]
US 20240002246A1 · Luis Alconero et al. · 2024 [cited by applicant]
US 20240182340A1 · Atwater et al. · 2024 [cited by applicant]
US 20240198280A1 · Behr · 2024 [cited by applicant]
US 20240238721A1 · Cohen-Cole et al. · 2024 [cited by applicant]
US 20240252980A1 · Ding et al. · 2024 [cited by applicant]
US 20240368776A1 · Berlinguette et al. · 2024 [cited by applicant]
US 20240392449A1 · Berlinguette et al. · 2024 [cited by applicant]
US 20240424446A1 · Gobaille-Shaw et al. · 2024 [cited by applicant]
US 20250018340A1 · Zhao et al. · 2025 [cited by applicant]
US 20250018341A1 · Lv · 2025 [cited by applicant]
US 20250050273A1 · Lackner · 2025 [cited by applicant]
US 20250108330A1 · Cai · 2025 [cited by applicant]
US 20250128204A1 · Kawatra et al. · 2025 [cited by applicant]
US 20250144563A1 · Sahay · 2025 [cited by applicant]
US 20250161866A1 · Behr · 2025 [cited by applicant]
US 20250170518A1 · Jakobsen et al. · 2025 [cited by applicant]
US 20250188626A1 · Kawatra et al. · 2025 [cited by applicant]
US 20250283231A1 · Zhang et al. · 2025 [cited by applicant]
US 20250325939A1 · Cohen-Cole et al. · 2025 [cited by applicant]
US 20250332539A1 · Robinson et al. · 2025 [cited by applicant]
CA 2592926 · 2009 [cited by applicant]
EP 2163294 · 2010 [cited by applicant]
JP 2012096975 · 2012 [cited by applicant]
WO WO2006036396 · 2006 [cited by applicant]
WO WO2012050530A1 · 2012 [cited by applicant]
WO WO2017205044 · 2017 [cited by applicant]
WO WO2019204938 · 2019 [cited by applicant]
WO WO2022040784 · 2022 [cited by applicant]
WO WO2022192501 · 2022 [cited by applicant]
WO WO2022195299 · 2022 [cited by applicant]
WO WO2023245195A2 · 2023 [cited by applicant]
WO WO2024017932A1 · 2024 [cited by applicant]
WO WO2024110882A1 · 2024 [cited by applicant]
WO WO2024118103A1 · 2024 [cited by applicant]
WO WO2024133948A1 · 2024 [cited by applicant]
WO WO2024165228A1 · 2024 [cited by applicant]
WO WO2024175854A1 · 2024 [cited by applicant]
WO WO2024234105A1 · 2024 [cited by applicant]
WO WO2025016957A1 · 2025 [cited by applicant]
WO WO2025120568A1 · 2025 [cited by applicant]
WO WO2025155846A1 · 2025 [cited by applicant]
WO WO2025202474A1 · 2025 [cited by applicant]
Invitation to Pay Additional Fees in International Application No. PCT/US2022/027523, mailed on Aug. 5, 2022, 21 pages. [cited by applicant]
International Preliminary Report on Patentability in International Application No. PCT/US2022/027523, mailed on Nov. 16, 2023, 18 pages. [cited by applicant]
Bandi et al., “CO [cited by applicant]
International Search Report and Written Opinion in International Application No. PCT/US2022/027523, mailed on Sep. 28, 2022, 27 pages. [cited by applicant]
Choi et al., “Membrane distillation crystallization for brine mining and zero liquid discharge: opportunities, challenges, and recent progress,” Environ. Sci. Water Res. Technol., 2019, 5(7):1202-1221. [cited by applicant]
Eisaman et al., “CO2 desorption using high-pressure bipolar membrane electrodialysis,” Energy Environ. Sci., 2011, 4(10):4031-4037. [cited by applicant]
Eisaman et al., “CO2 extraction from seawater using bipolar membrane electrodialysis,” Energy Environ. Sci., 2012, 5(6):7346-7352. [cited by applicant]
Eisaman et al., “CO2 separation using bipolar membrane electrodialysis,” Energy Environ. Sci., Apr. 2011, 4(4):1319-1328. [cited by applicant]
Fink et al., “Electrolytic conversion of carbon capture solutions containing carbonic anhydrase,” J. Inorg. Biochem., 2022, 231(111782), 7 pages. [cited by applicant]
Genders, “Electrochemical salt splitting,” Watts New Quarterly Newsletter, Sep. 1995, 1(1), 8 pages. [cited by applicant]
Giner, Inc., “Direct Air Capture Utilizing Hydrogen-Assisted Carbonate Electrolysis.” U.S. Department of Energy—Categorical Exclusion Determination Form, May 2021, 1 page. [cited by applicant]
Iizuka et al., “Carbon dioxide recovery from carbonate solutions using bipolar membrane electrodialysis,” Sep. Purif. Technol., 2012, 101:49-59. [cited by applicant]
Jaroszek et al., “Ion-exchange membranes in chemical synthesis—a review,” Open Chemistry, Dec. 2015, 14(1):1-19. [cited by applicant]
Li et al., “CO2 electroreduction from carbonate electrolyte,” ACS Energy Lett., May 2019, 4:1427-1431. [cited by applicant]
Li et al., “Electrolytic conversion of bicarbonate into CO in a flow cell,” Joule, Jun. 2019, 3:1487-1497. [cited by applicant]
Nagasawa et al., “A new recovery process of carbon dioxide from alkaline carbonate solution via electrodialysis,” AIChE J., Dec. 2009, 55(12):3286-3293. [cited by applicant]
Prajapati et al., “Migration-assisted, moisture gradient process for ultrafast, continuous CO2 capture from dilute sources at ambient conditions,” Energy Environ. Sci, Jan. 2022, 15(2): 680-692, 3 pages (Abstract only). [cited by applicant]
Shen et al., High performance electrospun bipolar membrane with a 3D junction, Energy Environ. Sci, 2017, 1435-1442, 27 pages. [cited by applicant]
Shuangchen et al., “Experimental study on desorption of simulated solution after ammonia carbon capture using bipolar membrane electrodialysis,” Int. J. Greenh. Gas Control, 2015, 42:690-698. [cited by applicant]
Shuto et al., “CO2 Fixation Process with Waste Cement Powder via Regeneration of Alkali and Acid by Electrodialysis: Effect of Operation Conditions,” Ind. Eng. Chem. Res., 2015, 54(25):6569-6577. [cited by applicant]
Škrtić et al., “Continuous crystallization of potassium carbonate,” Chem. Eng. Technol., 1989, 12(1):345-350. [cited by applicant]
Wei et al., “Comparative study on regenerating sodium hydroxide from the spent caustic by bipolar membrane electrodialysis (BMED) and electro-electrodialysis (EED),” Sep. Purif. Technol., 2013, 118:1-5. [cited by applicant]
Wei et al., “Regenerating sodium hydroxide from the spent caustic by bipolar membrane electrodialysis (BMED),” Sep. Purif. Technol., 2012, 86: 49-54. [cited by applicant]
Wilhelm, “Bipolar Membrane Electrodialysis: Membrane Development and Transport Characteristics,” Ph.D. thesis, University of Twente, 2001, 242 pages. [cited by applicant]
Wu et al., “Precipitating Characteristics of Potassium Bicarbonate Using Concentrated Potassium Carbonate Solvent for Carbon Dioxide Capture. Part 1. Nucleation,” Ind. Eng. Chem. Res., 2017, 56(23):6764-6774. [cited by applicant]
Ye et al., “Environmental evaluation of bipolar membrane electrodialysis for NaOH production from wastewater: Conditioning NaOH as a CO2 absorbent,” Sep. Purif. Technol., 2015, 144, 206-214. [cited by applicant]
Ye et al., “Kinetic behavior of potassium bicarbonate crystallization in a carbonate-based CO2 absorption process,” Chem. Eng. Res. Des., 2015, 93:136-147. [cited by applicant]
Ye et al., “Membrane Crystallization of Sodium Carbonate for Carbon Dioxide Recovery: Effect of Impurities on the Crystal Morphology,” Cryst. Growth Des., 2013, 13(6):2362-2372. [cited by applicant]
Office Action in Australian Appln. No. 202270091, mailed on Sep. 22, 2025, 5 pages. [cited by applicant]
Office Action in European Appln. No. 22725055.9, mailed on Oct. 17, 2025, 10 pages. [cited by applicant]
AU Office Action in Australian Appln. No. 2022270091, mailed on Mar. 4, 2026, 7 pages. [cited by applicant]