IP Library › Granted Patent US 9,242,205
Granted Patent B2
US 9,242,205 · App. 13/519,514 · Granted Jan 26, 2016

Alkali-carbonate-based carbon dioxide absorbent containing added sterically hindered cyclic amines, and method for removing carbon dioxide removing using same

Inventors: Yeo-Il Yoon (Daejeon, KR); Sung-Chan Nam (Daejeon, KR); Young-Eun Kim (Daejeon, KR); Il-Hyun Baek (Daejeon, KR); Sang-Do Park (Daejeon, KR)
Assignee: KOREA INSTITUTE OF ENERGY RESEARCH
B01D53/1475B01D53/1493B01D53/62B01D2251/306B01D2251/606B01D2252/2041B01D2252/20426B01D2252/20447B01D2252/504B01D2257/504Y02C10/04Y02C10/06
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Quick Facts
Patent No.
US 9,242,205
App. No.
13/519,514
Granted
Jan 26, 2016
Kind
B2
Abstract

The present invention relates to a carbon dioxide absorbent, and more particularly, to an alkali carbonate-based carbon dioxide absorbent containing added sterically hindered cyclic amines, and to a method for removing carbon dioxide using same. By adding sterically hindered cyclic amines to an alkali carbonate material, the rate of carbon dioxide absorption is increased, renewable energy is reduced, and salt production and phase separation do not occur.

Claims (10)

1. A method for removing carbon dioxide comprising:

contacting a gas containing carbon dioxide with a carbon dioxide absorbent containing an added sterically hindered cyclic amine;

absorbing carbon dioxide from the gas; and

regenerating the carbon dioxide absorbent,

wherein the carbon dioxide absorbent includes 16 or less wt % of potassium carbonate (K 2 CO 3 ) and 10 or less wt % of a sterically hindered cyclic amine; and

wherein the sterically hindered cyclic amine has a boiling point of 145° C. or more and a solubility of 500 grains/liter (g/l) or more in water at 25° C.

2. The method of claim 1 , wherein the sterically hindered cyclic amine is at least one selected from a group consisting of 1-amino-4methyl piperazine, 1-(2-aminoethyl)-4methyl piperazine, 1-(2-hydroxyethyl)-4methyl piperazine, 1-(2-aminoethyl)-piperazine, 1-(2-hydroxyethyl)-piperazine, 2-aminoethyl-piperazine, 1-ethyl-piperazine, 2,5-dimethyl-piperazine, cis 2,6-dimethyl-piperazine, 1,4-dimethyl-piperazine, trans 2,5-dimethyl-piperazine, 1-methyl piperazine, 2-methyl piperazine, 1-ethyl piperazine, 2-piperidine ethanol, 3-piperidine ethanol, 4-piperidine ethanol, 2-aminoethyl-1-piperidine, and homopiperazine.

3. The method of claim 2 , wherein the carbon dioxide absorbent further includes a corrosion inhibitor, a flocculation aid, an antioxidant, an antifoaming agent, or mixtures thereof.

4. The method of claim 2 , wherein the absorbing of carbon dioxide is performed in the pressure range between 1 to 30 atmosphere and the temperature range between 20 to 90° C.

5. The method of claim 2 , wherein the regenerating of the carbon dioxide absorbent is performed in the pressure range of 1 to 10 atmospheres (atm) and the temperature range of 105 to 120° C.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 9, 2012
From: YOON, YEO-IL; NAM, SUNG-CHAN; KIM, YOUNG-EUN; BAEK, IL-HYUN; PARK, SANG-DO
To: KOREA INSTITUTE OF ENERGY RESEARCH
Reel/Frame 028755/0937 →
Priority Claims (1)
KR 10-2009-0131571 · Dec 28, 2009 · national
Continuity (1)
Related Publication 20120308457A1 · Dec 6, 2012