Regenerable solid amine sorbent

• US 5,876,488 A
• Filed: 10/22/1996
• Issued: 03/02/1999
• Est. Priority Date: 10/22/1996
• Status: Expired due to Fees

• Current Assignee: United Technologies Corporation (Raytheon Technologies Corporation d/b/a RTX)
• Original Assignee: United Technologies Corporation (Raytheon Technologies Corporation d/b/a RTX)
• Inventors: Nalette, Timothy A., Birbara, Philip J., Filburn, Thomas P.
• Primary Examiner(s): SPITZER, ROBERT H
• Application Number:
  US08/734,904
• Time in Patent Office: 861 Days
• Field of Search: 95/139, 95/117, 95/121, 95/122, 96/109, 96/111, 96/115, 96/130, 422/171, 422/177, 422/178, 422/196, 423/228-230
• US Class Current: 96/111
• CPC Class Codes: B01D 2257/504 Carbon dioxide
• CPC Class Codes: B01D 2259/4575 in aeroplanes or space ships
• CPC Class Codes: B01D 2259/65 Employing advanced heat integration, e.g. Pinch technology
• CPC Class Codes: B01D 53/0415 Beds in cartridges
• CPC Class Codes: B01D 53/0438 Cooling or heating systems
• CPC Class Codes: B01J 20/28057 Surface area, e.g. B.E.T specific surface area
• CPC Class Codes: B01J 20/28078 Pore diameter
• CPC Class Codes: B01J 20/321 consisting of a polymer obtained by reactions involving only carbon to carbon unsaturated bonds
• CPC Class Codes: B01J 20/3217 Resulting in a chemical bond between the coating or impregnating layer and the carrier, support or substrate, e.g. a covalent bond
• CPC Class Codes: B01J 20/3251 comprising at least two different types of heteroatoms selected from nitrogen, oxygen or sulphur
• CPC Class Codes: B01J 20/3255 comprising a cyclic structure containing at least one of the heteroatoms nitrogen, oxygen or sulfur, e.g. heterocyclic or heteroaromatic structures
• CPC Class Codes: B01J 20/3425 of sorbents or filter aids comprising organic materials
• CPC Class Codes: B01J 20/3458 in the gas phase
• CPC Class Codes: B01J 20/3483 by thermal treatment not covered by groups B01J20/3441 - B01J20/3475, e.g. by heating or cooling
• CPC Class Codes: B01J 20/3491 by pressure treatment
• CPC Class Codes: B01J 2220/56 Use in the form of a bed
• CPC Class Codes: Y02C 20/40 of CO2

Abstract

The invention provides a regenerable supported amine sorbent having an amine concentration of from about 35 wt. % to about 75 wt. %. The balance of the sorbent is a porous support which provides the sorbent with structural rigidity and a surface for gas/solid contact. The invention further provides a process for making the sorbent and system for cyclically absorbing and desorbing carbon dioxide using a plurality of sorbent beds.

Claims

1. A system for cyclically absorbing and desorbing carbon dioxide and water vapor, said system comprising:

first and second sorbent beds, each bed containing a supported regenerable amine sorbent comprising from about 35 wt. % to about 75 wt. % amine, said amine selected from the group consisting of primary amines, secondary amines, and mixtures thereof including a plurality of hydoxyl (--OH) groups, and an acrylic ester resin porous support for providing structural integrity to the amine;

a plurality of valves for directing a gas stream into and out of each sorbent bed and for exposing each bed to a pressure gradient;

a thermal conductor for conducting heat between the beds;

a sensor for detecting the concentration of carbon dioxide in each bed; and

a controller responsive to one of the sensor and a predetermined time period for controlling operation of the plurality of valves so that one of the beds is in the absorption cycle while the second bed is in the desorption cycle.

2. A supported regenerable amine sorbent comprising from about 35 wt. % to about 75 wt. % amine, said amine selected from the group consisting of primary amines, secondary amines, and mixtures thereof including a plurality of hydoxyl (--OH) groups, and an acrylic ester resin porous support for providing the amine with structural integrity and a surface for gas/solid contact.

3. The sorbent of claim 2, wherein the amine is selected from the group consisting of diethanolamine (DEA), diisopropanolamine (DIPA), 2-hydoxyethyl piperazine (HEP), and mixtures thereof.

4. The sorbent of claim 3, wherein the amine is diethanolamine.

5. The sorbent of claim 4, wherein the diethanolamine is present in a concentration of about 53 wt. %.

6. The sorbent of claim 2, wherein the amine is present in a concentration of from about 45 wt. % to about 65 wt. %.

7. The sorbent of claim 2, wherein the porous support has a surface area of from about 50 m² /g to about 1,000 m² /g.

8. A supported regenerable amine sorbent comprising from about 45 wt. % to about 65 wt. % amine selected from the group consisting of diethanolamine (DEA), diisopropanolamine (DIPA), 2-hydoxyethyl piperazine (HEP), and mixtures thereof, the remainder of the sorbent being a porous acrylic ester resin for providing structural integrity to the amine and a surface for gas/solid contact.

9. The sorbent of claim 8 comprising about 53 wt. % diethanolamine and about 47 wt. % acrylic ester resin.

10. A process for making a regenerable supported amine sorbent, said process comprising the steps of:

forming an amine/solvent solution, said amine selected from the group consisting of primary amines, secondary amines, and mixtures thereof including a plurality of hydoxyl (--OH) groups;

mixing an acrylic ester resin porous support material with the amine solution;

heating the mixture to both retain the amine on the support and remove the solvent from the mixture, and thereby form the sorbent.

11. The process of claim 10 further including the step of evaporating the solvent from the mixture.

12. The process of claim 10, wherein the amine is selected from the group consisting of diethanolamine (DEA), diisopropanolamine (DIPA), 2-hydoxyethyl piperazine (HEP), and mixtures thereof.

13. The process of claim 10, wherein the amine is diethanolamine.

14. The process of claim of claim 10, wherein the step of heating is further characterized in that the mixture is heat to a temperature in the range of from about 70°

C. to about 100°

C.

15. The process of claim 14, wherein the mixture is heated to a temperature in the range of from about 90°

C. to about 95°

C.

16. The process of claim 10, wherein the step of heating the mixture is further characterized in that the sorbent comprises from about 35 wt. % to about 75 wt. % amine.

17. The process of claim 10, wherein the step of forming the amine solution is further characterized in that the solvent is selected from the group consisting of alcohol-based solvents, non-reactive solvents, and aqueous solvents.

18. The process of claim 17, wherein the solvent is methanol.