METHODS FOR DEACIDIZING GASEOUS MIXTURES BY PHASE ENHANCED ABSORPTION

• US 20110229393A1
• Filed: 04/13/2011
• Published: 09/22/2011
• Est. Priority Date: 04/07/2006
• Status: Active Grant

• Current Assignee: Liang Hu
• Original Assignee: Liang Hu
• Inventors: HU, Liang
• Granted Patent: US 8,318,116 B2
• Time in Patent Office: Days
• US Class Current: 423/220
• CPC Class Codes: B01D 2252/103 Water
• CPC Class Codes: B01D 2252/202 Alcohols or their derivatives
• CPC Class Codes: B01D 2252/20405 Monoamines
• CPC Class Codes: B01D 2252/2041 Diamines
• CPC Class Codes: B01D 2257/504 Carbon dioxide
• CPC Class Codes: B01D 53/1425 Regeneration of liquid absorbents
• CPC Class Codes: B01D 53/1493 Selection of liquid materials for use as absorbents

Abstract

An improved process for deacidizing a gaseous mixture using phase enhanced gas-liquid absorption is described. The process utilizes a multiphasic absorbent that absorbs an acid gas at increased rate and leads to reduced overall energy costs for the deacidizing operation.

Claims

1. A method for deacidizing a gaseous mixture comprising an acid gas, the process comprising:

contacting the gaseous mixture with an absorbent in an absorption unit, wherein the absorbent comprises a carrier phase and a transportation phase that is immiscible with or mechanically separable from the carrier phase;

allowing the transportation phase to absorb the acid gas and convert the acid gas into an absorbed acid gas, so as to convert the absorbent into a gas-rich absorbent and to convert the gaseous mixture into a purified gaseous mixture;

allowing the absorbed acid gas to be transferred into the carrier phase, so as to form a first gas-lean phase and a gas-rich phase in the gas-rich absorbent;

providing the gas-rich absorbent to a separation unit, so as to separate the first gas-lean phase from the gas-rich phase;

cycling the separated first gas-lean phase back into the absorption unit;

providing the separated gas-rich phase to a regeneration unit, so as to obtain the acid gas and a second gas-lean phase; and

cycling the second gas-lean phase back into the absorption unit.

2. The method of claim 1, wherein the transportation phase comprises one or more components selected from the group consisting of organofluorous solvents, organosilicon solvents, polymers, ionic liquids, an alkane, an unsaturated hydrocarbon, an alcohol, a glycol, an ether, a glycol ether, an aldhyde, a ketone, a carbohydrate, alkylene carbonates, dialky carbonates, sulfolane, an amine, an alkanolamine, an amino acid and amino acid salt, water, alkaline salts, ammonium salts, alkanolamine salts, or alkaline-earth salts, urea, alkaline metal phosphates, carbonates, borates, acid phosphites, phosphites, phosphonite, phosphinate, phosphonate, acid phosphates, pyrophosphites, bicarbonates, metaborates, diborates, tetraborates, pentaborates, and derivatives thereof or combinations thereof.

3. The method of claim 1, wherein the carrier phase is hydrophilic or hydrophobic.

4. The method of claim 1, wherein the carrier phase comprises one or more components selected from the group consisting of an amine salt, an ammonium salt, an alkanolamine salt, an alkaline salt, an alkaline-earth salt, an amino acid salt, a reaction product of amino acid salt with acid gas, such as, CO₂, urea, alkaline metal phosphates, carbonates, borates, acid phosphites, phosphites, phosphonite, phosphinate, phosphonate, acid phosphates, pyrophosphites, bicarbonates, metaborates, diborates, tetraborates, pentaborates, water and derivatives thereof, or combinations thereof.

5. The method of claim 1, wherein the carrier phase comprises a component selected from the group consisting of a monoethanolamine salt, a diethanolamine salt, a piperizine salt, a dibutylamine salt, a diisopropylamine salt, a potassium bicarbonate, a sodium bicarbonate and a potassium carbonate, and a sodium carbonate.

6. The method of claim 1, wherein the gas-rich phase is regenerated by a process selected from the group consisting of thermal decomposition, gas stripping, steam stripping, distillation, treatment through a membrane contactor, pervaporization, microwave, supersonic, extrusion, stir, pressure differential treatment, and a combination thereof.

7. The method of claim 1, wherein the acid gas is selected from the group consisting of CO₂, SO₂, H₂S, COS, C₂S, mercaptans, fluorides, NO_X, SO_X, and HCl.

8. The method of claim 7, wherein the acid gas is CO₂.

9. The method of claim 1, wherein the transportation phase absorbs the acid gas physically, chemically, or both physically and chemically.

10. The method of claim 1, wherein the first gas-lean phase and the second gas-lean phase are mixed together before they are cycled back into the absorption unit.

11. The method of claim 1, wherein the gas-rich absorbent is provided to the separation unit before, after, or simultaneously with the transfer of the absorbed acid gas into the carrier phase, thus the formation of the first gas-lean phase and the gas-rich phase.

12. The method of claim 1, wherein the gas-rich absorbent moves downward from the absorption unit to the separation unit by gravity.

13. The method of claim 1, wherein the separated gas-rich phase moves downward from the separation unit to the regeneration unit by gravity.

14. The method of claim 1, wherein the transportation phase comprises a component selected from the group consisting of monoethanolamine, diethanolamine, piperizine, dibutylamine, and diisopropylamine, wherein the component is dissolved in at least one of a glycol, a glycol ether, a C₈-C₁₂ alcohol, decamethyltetrasiiloxane, and dedecamethyltetrasiloxine.

15. A method for deacidizing a gaseous mixture comprising an acid gas, the process comprising:

contacting the gaseous mixture with an absorbent in an absorption unit, wherein the absorbent comprises a carrier phase and a transportation phase that is immiscible with or mechanically separable from the carrier phase;

allowing the transportation phase to absorb the acid gas and convert the acid gas into an absorbed acid gas, so as to convert the absorbent into a gas-rich absorbent and to convert the gaseous mixture into a purified gaseous mixture;

allowing the absorbed acid gas to be transferred into the carrier phase, so as to form a first gas-lean phase and a gas-rich phase in the gas-rich absorbent;

providing the gas-rich absorbent to a separation unit, so as to separate the first gas-lean phase from the gas-rich phase;

cycling the separated first gas-lean phase back into the absorption unit;

providing the separated gas-rich phase to a regeneration unit, so as to obtain the acid gas and a second gas-lean phase; and

cycling the second gas-lean phase back into the absorption unit,

wherein the absorbent comprises a pair of the transportation phase and the carrier phase selected from the group consisting of;

(1) a solution of at least one of monoethanolamine, diethanolamine, methyl diethanolamine, piperizine, dibutylamine, diisopropylamine in at least one of an alcohol, a glycol ether and a glycol, and one or more reaction products of monoethanolamine, diethanolamine, methyl diethanolamine, piperizine, dibutylamine, diisopropylamine with CO2;

(2) a solution of at least one of monoethanolamine, diethanolamine, methyl diethanolamine, piperizine, dibutylamine, diisopropylamine in at least one of an alcohol, a glycol ether and a glycol, and an aqueous solution of one or more reaction products of monoethanolamine, diethanolamine, methyl diethanolamine, piperizine, dibutylamine, diisopropylamine with CO2;

(3) a solution of at least one of monoethanolamine, diethanolamine, methyl diethanolamine, piperizine, dibutylamine, diisopropylamine in at least one of an alcohol, a glycol ether and a glycol, and one or more reaction products of monoethanolamine, diethanolamine, methyl diethanolamine, piperizine, dibutylamine, diisopropylamine with CO2;

(4) a solution of at least one of monoethanolamine, diethanolamine, methyl diethanolamine, piperizine, dibutylamine, diisopropylamine in at least one of an alcohol, a glycol ether and a glycol, and an aqueous solution of potassium carbonate; and

(5) a solution of at least one of amine, amino-acid salt, potassium carbonate, or sodium carbonate in water, and potassium bicarbonate, potassium carbonate, sodium bicarbonate, or sodium carbonate.

16. A method for deacidizing a gaseous mixture comprising an acid gas, the process comprising:

contacting the gaseous mixture with an absorbent in an absorption unit, wherein the absorbent comprises a carrier phase and a transportation phase that is immiscible with or mechanically separable from the carrier phase;

allowing the transportation phase to absorb the acid gas and convert the acid gas into an absorbed acid gas, so as to convert the absorbent into a gas-rich absorbent and to convert the gaseous mixture into a purified gaseous mixture;

allowing the absorbed acid gas to be transferred into the carrier phase, so as to form a first gas-lean phase and a gas-rich phase in the gas-rich absorbent;

providing the gas-rich absorbent to a separation unit, so as to separate the first gas-lean phase from the gas-rich phase;

cycling the separated first gas-lean phase back into the absorption unit;

providing the separated gas-rich phase to a regeneration unit, so as to obtain the acid gas and a second gas-lean phase; and

cycling the second gas-lean phase back into the absorption unit,

wherein the absorption of the acid gas from the gaseous mixture and the transportation of the absorbed acid gas to the carrier phase occur in one unit or multiple units, the carrier phase exists before, during or after the absorption of the acid gas, and the transportation phase exists before, during or after the absorption of the acid gas.

17. The method of claim 16, wherein the carrier phase occurs with or without changing operation conditions, and that the carrier phase occurs in the gas absorption unit, the separation unit or both the gas absorption unit and the separation unit.

18. The method of claim 16, wherein the transportation phase disappears during absorption or after absorption.

19. The method of claim 18, wherein the transportation phase evaporates or is converted into the carrier phase after the absorbed acid is transferred into the carrier phase.