IP Library Granted Patent US 8,535,502
Granted Patent B2
US 8,535,502 · App. 12/206,424 · Granted Sep 17, 2013

System and method for recovery of CO

Inventors: Karl A. Littau (Palo Alto, CA); Francisco E. Torres (San Jose, CA)
Assignee: Palo Alto Research Center Incorporated
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,535,502
App. No.
12/206,424
Granted
Sep 17, 2013
Kind
B2
Abstract

A system and method for recovery of CO 2 includes an aqueous capture device having a capture solution. The aqueous capture device is arranged to receive gas and to capture components from the gas including at least CO 2 . An electrodialysis unit in operative connection with the capture device performs an electrodialysis operation on the capture solution including at least the CO 2 , wherein a CO 2 rich process stream and a regenerated capture solution are generated from the capture solution including at least the CO 2 . The CO 2 rich process stream is a pressurized process stream at a pressure which maintains the CO 2 substantially within the CO 2 rich process stream, while in the electrodialysis unit. In another alternative, at least the pH of the capture stream is controlled.

Claims (39)

1. A system for recovery of CO 2 comprising:

an aqueous capture device including a capture solution, the aqueous capture device arranged to receive gas and to capture components from the gas including at least CO 2 ;

an electrodialysis unit in operative connection with the capture device to perform an electrodialysis operation on the capture solution including at least the CO 2 ; and

monitors for monitoring pH of the system,

wherein:

a CO 2 rich process stream and a regenerated capture solution are generated from the capture solution including at least the CO 2 , the regenerated capture solution being sent back to the aqueous capture device,

the CO 2 rich process stream is a pressurized process stream at a pressure which maintains the CO 2 in a solution state substantially within the CO 2 rich process stream, while in the electrodialysis unit,

the CO 2 rich process is a buffered process stream having a pH ranging from about 3 to 4 while in the electrodialysis unit, and

the capture solution is a buffered process stream having a pH ranging from about 8 to about 10 while in the electrodialysis unit.

2. The system according to claim 1 wherein the system is a closed loop system.

3. The system according to claim 1 , further including a controller to control the flow rate of the capture solution, dependent on signals provided from the monitors.

4. The system according to claim 1 wherein the electrodialysis unit is a bipolar membrane electrodialysis unit.

5. The system according to claim 1 , wherein the aqueous capture device is a pressure aqueous capture device, which operates at a pressure high enough for operation of the electrodialysis unit, which is a bipolar membrane electrodialysis unit.

6. The system according to claim 1 , further including, a gas evolution/separation tank in operative connection with the electrodialysis unit and configured to receive the CO 2 rich process stream, the CO 2 rich process stream being at least partially de-pressurized and CO 2 gas being removed, the CO 2 depleted process stream being sent back to the electrodialysis unit.

7. The system of claim 1 , wherein:

the capture solution is an aqueous carbonate/bicarbonate solution, MX;

the electrodialysis unit comprises at least one membrane capable of transporting carbonate/bicarbonate ions; and

the electrodialysis unit is configured so as to transport carbonate/bicarbonate ions X − from the capture solution across the at least one membrane into the CO 2 rich process stream.

8. A method for recovering CO 2 comprising:

receiving, in an aqueous capture device, a gas;

capturing at least portions of the gas including at least CO 2 by a capture solution in the aqueous capture device;

performing an electrodialysis operation on the capture solution by an electrodialysis unit; and

monitoring at least the pH of the capture solution and the CO 2 rich process stream,

wherein:

a CO 2 rich process stream and a regenerated capture solution are generated from the capture solution including at least CO 2 ,

the CO 2 rich process stream is a pressurized process stream at a pressure which maintains the CO 2 in a solution state substantially within the CO 2 rich process stream while in the electrodialysis unit,

the CO 2 rich process stream is a buffered process stream having a pH ranging from about 3 to about 4 while in the electrodialysis unit, and

the capture solution is a buffered process stream having a pH ranging from about 8 to about 10 while in the electrodialysis unit.

9. The method according to claim 8 , further including:

moving the regenerated capture solution back to the aqueous capture device, the regenerated capture solution being substantially depleted of CO 2 ;

at least partially de-pressurizing the CO 2 rich process stream by a gas evolution/separation tank to remove CO 2 from the process stream; and

moving the CO 2 depleted process stream back through the electrodialysis unit.

10. The method according to claim 9 wherein a pressure is applied to the capture solution which is sufficient to substantially eliminate evolving of the CO 2 from the CO 2 rich process stream while the CO 2 rich process stream is being processed by the electrodialysis unit.

11. The method according to claim 8 wherein the pressure of the CO 2 rich process stream is between 2-200 atm.

12. The method according to claim 8 further providing a buffered process stream within the electrodialysis unit.

13. The method of claim 8 , wherein:

the capture solution is an aqueous carbonate/bicarbonate solution, MX;

the electrodialysis unit comprises at least one membrane capable of transporting carbonate/bicarbonate ions; and

the electrodialysis unit is configured so as to transport carbonate/bicarbonate ions X − from the capture solution across the at least one membrane into the CO 2 rich process stream.

Assignments (9)
SECOND LIEN NOTES PATENT SECURITY AGREEMENT Recorded Jul 2, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 071785/0550 →
FIRST LIEN NOTES PATENT SECURITY AGREEMENT Recorded Apr 11, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 070824/0001 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT RF 064760/0389 Recorded Feb 13, 2024
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: XEROX CORPORATION
Reel/Frame 068261/0001 →
SECURITY INTEREST Recorded Feb 13, 2024
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 066741/0001 →
SECURITY INTEREST Recorded Nov 20, 2023
From: XEROX CORPORATION
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 065628/0019 →
CORRECTIVE ASSIGNMENT TO CORRECT THE REMOVAL OF US PATENTS 9356603, 10026651, 10626048 AND INCLUSION OF US PATENT 7167871 PREVIOUSLY RECORDED ON REEL 064038 FRAME 0001. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 28, 2023
From: PALO ALTO RESEARCH CENTER INCORPORATED
To: XEROX CORPORATION
Reel/Frame 064161/0001 →
SECURITY INTEREST Recorded Jun 22, 2023
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 064760/0389 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 20, 2023
From: PALO ALTO RESEARCH CENTER INCORPORATED
To: XEROX CORPORATION
Reel/Frame 064038/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 8, 2008
From: LITTAU, KARL A.; TORRES, FRANCISCO E.
To: PALO ALTO RESEARCH CENTER INCORPORATED
Reel/Frame 021496/0787 →
Continuity (1)
Related Publication 20100059377A1 · Mar 11, 2010