IP Library Granted Patent US 11,512,403
Granted Patent B2
US 11,512,403 · App. 16/254,255 · Granted Nov 29, 2022

System and method for carbon dioxide reactor control

Inventors: Kendra Kuhl (Oakland, CA); Etosha Cave (Berkeley, CA); Nicholas Flanders (San Francisco, CA); Sichao Ma (Dublin, CA); Qun Zeng (Oakland, CA); George Leonard (Oakland, CA)
Assignee: Twelve Benefit Corporation
C25B15/02C25B1/02C25B9/23C25B9/70C25B11/031
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Quick Facts
Patent No.
US 11,512,403
App. No.
16/254,255
Granted
Nov 29, 2022
Kind
B2
Abstract

A system preferably including a carbon dioxide reactor. A method for carbon dioxide reactor control, preferably including selecting carbon dioxide reactor aspects based on a desired output composition, running a carbon dioxide reactor under controlled process conditions to produce a desired output composition, and/or altering the process conditions to alter the output composition.

Claims (57)

1. A method for electrolyzer control comprising, at a gas-phase electrolyzer, electrochemically producing a reduction product comprising molecular hydrogen and a carbon-containing species (CCS) from an input comprising gas-phase carbon dioxide, wherein the CCS is a product of the electrochemical reduction of carbon dioxide, wherein the gas-phase electrolyzer comprises a cathode layer having a reduction catalyst and an ion-conducting polymer in contact with a polymer electrolyte membrane and electrochemically producing the reduction product comprises:

during a first time interval, producing the reduction product with a first molecular hydrogen-to-CCS ratio (HCR), comprising operating the gas-phase electrolyzer including the reduction catalyst under a first set of process conditions; and

during a second time interval after the first time interval, adjusting electrolyzer operation to change the reduction product HCR, comprising operating the gas-phase electrolyzer including the reduction catalyst used during the first time interval under a second set of process conditions to produce the reduction product with a second HCR that differs from the first HCR by at least 1%.

2. The method of claim 1 , wherein:

during the first time interval, the input defines a first input gas hydration;

adjusting electrolyzer operation comprises altering the input gas hydration such that, during the second time interval, the input defines an input gas hydration greater than the first input gas hydration and

the second HCR is greater than the first HCR.

3. The method of claim 1 , wherein adjusting electrolyzer operation to change the reduction product HCR is performed in response to determining a desired HCR different from the first HCR.

4. The method of claim 3 , further comprising:

providing the reduction product to a downstream reactor; and

determining an operation metric associated with the downstream reactor;

wherein determining the desired HCR is performed based on the operation metric.

5. The method of claim 4 , wherein:

the downstream reactor is a bioreactor;

the input further comprises a sulfur-containing species (SCS), wherein a concentration of the SCS in the input is at least 5 ppm; and

the method further comprises providing the SCS, intermixed with the reduction product, to the bioreactor.

6. The method of claim 1 , wherein:

the first set of process conditions comprises a first electrolyzer temperature greater than 50° C. and a first input pressure greater than 10 atmospheres; and

the second set of process conditions comprises a second electrolyzer temperature greater than 50° C. and a second input pressure greater than 10 atmospheres.

7. The method of claim 1 , wherein:

during the first time interval, the input defines a first gas-phase carbon dioxide flow rate; and

adjusting electrolyzer operation comprises altering the input gas-phase carbon dioxide flow rate such that, during the second time interval, the input defines a second phase carbon dioxide flow rate different than the first phase carbon dioxide flow rate.

8. The method of claim 1 , wherein:

adjusting electrolyzer operation comprises altering the current density.

9. The method of claim 1 , wherein:

adjusting electrolyzer operation comprises altering the reactor pressure or input gas pressure.

10. The method of claim 1 , wherein:

adjusting electrolyzer operation comprises altering the reactor temperature.

11. The method of claim 1 , wherein the second HCR differs from the first HCR by 75-100%.

12. The method of claim 1 , wherein the second HCR differs from the first HCR by 40%-80%.

13. The method of claim 1 , wherein the second HCR differs from the first HCR by 20%-50%.

14. The method of claim 1 , wherein the second HCR differs from the first HCR by 5%-25%.

15. The method of claim 1 , wherein the wherein the second HCR differs from the first HCR by 2%-10%.

16. The method of claim 1 , wherein the wherein the second HCR differs from the first HCR by at least 5%.

17. The method of claim 1 , wherein the wherein the second HCR differs from the first HCR by at least 10%.

18. The method of claim 1 , wherein the during the second time interval, the input is substantially pure CO 2 .

19. The method of claim 1 , wherein during the second time interval, the input is substantially pure CO 2 that is hydrated.

20. The method of claim 1 , wherein the input during at least the first time interval comprises a sulfur-containing species (SCS), wherein a concentration of the SCS in the input is at least 5 ppm.

21. The method of claim 20 , wherein a SCS is intermixed with the reduction product during at least the first time interval.

22. The method of claim 1 , wherein the reduction product is provided in an output stream, the output stream further comprising unreacted CO 2 .

23. The method of claim 1 , wherein the reduction product comprises syngas.

24. The method of claim 1 , wherein the reduction product is provided to a downstream bioreactor.

25. The method of claim 1 , wherein the reduction product is provided in an output stream, and further comprising providing the output stream to a downstream system.

26. The method of claim 25 , wherein the entirety of the output stream is provided to the downstream system.

27. The method of claim 1 , wherein the polymer electrolyte membrane is a bipolar membrane.

28. The method of claim 1 , wherein the polymer electrolyte membrane is a monopolar membrane.

29. The method of claim 1 , wherein:

the first set of process conditions comprise a first input pressure greater than 100 psi; and

the second set of process conditions comprises second input pressure greater than 100 psi.

30. The method of claim 29 , wherein:

the first set of process conditions comprise a first input temperature greater than 25° C.; and

the second set of process conditions comprises second input temperature greater than 25° C.

31. The method of claim 1 , where the CCS is carbon monoxide (CO).

32. A method for electrolyzer control comprising, at a gas-phase electrolyzer, electrochemically producing a reduction product comprising molecular hydrogen and a carbon-containing species (CCS) from an input comprising gas-phase carbon dioxide, wherein the CCS is a product of the electrochemical reduction of carbon dioxide, wherein electrochemically producing the reduction product comprises:

during a first time interval, producing the reduction product with a first molecular hydrogen-to-CCS ratio (HCR), comprising operating the gas-phase electrolyzer under a first set of process conditions; and

during a second time interval after the first time interval, adjusting electrolyzer operation to change the reduction product HCR, comprising operating the gas-phase electrolyzer under a second set of process conditions to produce the reduction product with a second HCR that differs from the first HCR by at least 1%, wherein the input during at least one of the first time interval and the second time interval comprises a sulfur-containing species (SCS), wherein a concentration of the SCS in the input is at least 5 ppm.

33. The method of claim 32 , wherein the SCS is intermixed with the reduction product during the least one of the first time interval and the second time interval.

Assignments (5)
SECURITY INTEREST Recorded Jan 19, 2026
From: TWELVE BENEFIT CORPORATION
To: SUMITOMO MITSUI BANKING CORPORATION
Reel/Frame 074435/0926 →
CONFIRMATORY LICENSE Recorded Sep 28, 2024
From: OPUS 12, INC.
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 069067/0713 →
CHANGE OF NAME Recorded May 13, 2022
From: OPUS 12 INCORPORATED
To: TWELVE BENEFIT CORPORATION
Reel/Frame 060068/0332 →
CORRECTIVE ASSIGNMENT TO CORRECT THE NAME OF THE ASSIGNEE PREVIOUSLY RECORDED AT REEL: 049446 FRAME: 0243. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded May 21, 2021
From: KUHL, KENDRA; CAVE, ETOSHA; FLANDERS, NICHOLAS; MA, SICHAO; ZENG, QUN; GEORGE, LEONARD
To: OPUS 12 INCORPORATED
Reel/Frame 056327/0285 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 12, 2019
From: KUHL, KENDRA; CAVE, ETOSHA; FLANDERS, NICHOLAS; MA, SICHAO; ZENG, QUN; LEONARD, GEORGE
To: OPUS 12, INC.
Reel/Frame 049446/0243 →
Continuity (4)
Provisional Application 62685771 · Jun 15, 2018
Provisional Application 62619996 · Jan 22, 2018
Provisional Application 62620109 · Jan 22, 2018
Related Publication 20190226103A1 · Jul 25, 2019
Cited By (9)
US 12,209,322 US 12,264,402 US 12,286,716 US 12,320,022 US 12,359,325 US 12,416,088 US 12,421,392 US 12,460,310 US 12,577,690