IP Library › Granted Patent US 9,221,007
Granted Patent B2
US 9,221,007 · App. 13/675,979 · Granted Dec 29, 2015

Method and device for separating acid gases from a gas mixture

Inventors: Jörn Rolker (Alzenau, DE); Matthias Seiler (Griesheim, DE); Ralf Meier (Dortmund, DE); Udo Knippenberg (Marl, DE); Rolf Schneider (Gründau-Rothenbergen, DE); Muhammad Irfan (Erlensee, DE); Hari Prasad Mangalapally (Hanau, DE)
Assignee: Evonik Degussa GmbH
B01D53/1475B01D53/1425B01D53/1456B01D53/1493B01D2257/30B01D2257/504F23J2219/40
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Quick Facts
Patent No.
US 9,221,007
App. No.
13/675,979
Granted
Dec 29, 2015
Kind
B2
Abstract

The invention is directed to a method for separating acid gases from a gas mixture in which the gas mixture is contacted with an absorption medium which comprises water and at least one amine and has a phase-separation temperature in the range from 0 to 130° C. In addition, the invention is directed to a device which can be used for carrying out this method.

Claims (24)

1. A method for separating acid gases from a gas mixture, said method comprising:

a) absorbing acid gases by contacting the gas mixture with an absorption medium comprising water and at least one amine to obtain a loaded absorption medium, wherein absorption takes place in an absorber and the absorption medium:

i) shows phase separation into two liquid phases upon heating above a phase-separation temperature in the range of 0 to 130° C.;

ii) comprises at least one amine of formula (I):

wherein R 1 is hydrogen and R 2 is an alkyl radical having 1to 6 carbon atoms;

b) desorbing acid gases from the loaded absorption medium by stripping the loaded absorption medium with steam in a desorption column, wherein desorption is carried out at a temperature at which a phase separation into a water-rich liquid phase and a water-poor liquid phase occurs in the desorption column;

c) separating the water-rich liquid phase and water-poor liquid phase from one another;

d) feeding the water-rich liquid phase to an evaporator in which steam is generated with which acid gases are stripped in the desorption column; and

e) returning the water-poor liquid phase and water-rich liquid phase to the absorber as absorption medium.

2. The method of claim 1 , wherein the absorption medium comprises an amine that, at 100° C., has a solubility of less than 100 g of amine in 1 l of water.

3. The method of claim 1 , wherein R 2 the absorption medium comprises 25 to 85% by weight water and 15 to 75% by weight amines of formula (I).

4. The method of claim 1 , wherein the absorption medium comprises:

a) a first amine of formula (I), wherein R 1 is hydrogen and R 2 is an alkyl radical having 1 to 6 carbon atoms; and

b) a second amine of formula (I), for which R 1 is hydrogen and R 2 is a radical (CH 2 ) n NR 3 R 4 , where n=2 to 4, R 3 =hydrogen or alkyl radical having 1 to 4 carbon atoms, and R 4 =alkyl radical having 1 to 4 carbon atoms.

5. The method of claim 1 , wherein the absorption medium comprises 25 to 85% by weight water and 15 to 75% by weight amines of formula (I).

6. The method of claim 4 , wherein the absorption medium comprises 25 to 85% by weight water and 15 to 75% by weight amines of formula (I).

7. The method of claim 6 , wherein, in said second amine of formula (I), R 1 is hydrogen and R 2 is a radical (CH 2 ) n NR 3 R 4 , where n=2 to 4, R 3 =hydrogen, and R 4 =alkyl radical having 1 to 4 carbon atoms.

8. The method of claim 6 , wherein in said second amine of formula (I), R 1 is hydrogen and R 2 is a radical (CH 2 ) n NR 3 R 4 where n=2 to 4, R 3 =alkyl radical having 1 to 4 carbon atoms, and R 4 =alkyl radical having 1 to 4 carbon atoms.

9. The method of claim 1 , wherein absorption is carried out at a temperature in the range of 0° C. to 70° C., and the temperature of the absorption medium on entry into the absorber is below the phase-separation temperature.

10. The method of claim 9 , wherein desorption is carried out at a temperature in the range of 50° C. to 200° C.

11. The method of claim 9 , wherein desorption is carried out at a temperature in the range of 80° C. to 150° C.

12. The method of claim 1 , wherein absorption is carried out at a temperature in the range of 20° C. to 50° C., and the temperature of the absorption medium on entry into the absorber is below the phase-separation temperature.

13. The method of claim 12 , wherein desorption is carried out at a temperature in the range of 50° C. to 200° C.

14. The method of claim 12 , wherein desorption is carried out at a temperature in the range of 80° C. to 150° C.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 20, 2012
From: ROLKER, JORN; SEILER, MATTHIAS; MEIER, RALF; KNIPPENBERG, UDO; SCHNEIDER, ROLF; IRFAN, MUHAMMAD; MANGALAPALLY, HARI PRASAD
To: EVONIK DEGUSSA GMBH
Reel/Frame 029329/0620 →
Priority Claims (1)
DE 10 2011 086 252 · Nov 14, 2011 · national
Continuity (2)
Provisional Application 61560281 · Nov 15, 2011
Related Publication 20130118350A1 · May 16, 2013