Method and absorption medium for absorbing CO
View Patent ↗The absorption of CO 2 from a gas mixture by contacting the gas mixture with an absorption medium that comprises water and 5 to 50 wt % of amino acid salts of formula R 1 R 2 CHNHCH 2 COOK, in which R 1 and R 2 are n-alkyl radicals and the radicals R 1 and R 2 together have 2 to 4 carbon atoms, affords a high CO 2 absorption capacity per unit weight in the cyclical operation of absorption and desorption.
1. An absorption medium for absorbing CO 2 from a gas mixture, comprising water and 5 to 50 wt % of amino acid salts of formula (I):
R 1 R 2 CHNHCH 2 COOK (I)
in which R 1 and R 2 are n-alkyl radicals, and the radicals R 1 and R 2 together have 2 to 4 carbon atoms;
which further comprises potassium ions in the form of potassium carbonate or potassium hydrogen carbonate, wherein the molar ratio of potassium ions in the form of potassium carbonate or potassium hydrogen carbonate to amino acid salts of formula I is in the range from 0.01 to 0.1;
and wherein: more than 90 wt % of the amino acid salts of formula (I) are potassium N-isopropylglycinate.
2. The absorption medium of claim 1 , further comprising a corrosion inhibitor, a wetting promoter and/or a defoamer.
3. The absorption medium of claim 1 , comprising 10 to 48 wt % of amino acid salts of formula (I).
4. The absorption medium of claim 1 , comprising 35 to 45 wt % of amino acid salts of formula (I).
5. The absorption medium of claim 1 , comprising more than 40 wt % of water.
6. A process for absorbing CO 2 from a gas mixture by contacting the gas mixture with the absorption medium of claim 1 .
7. The process of claim 6 , wherein the absorption medium comprises 10 to 48 wt % of amino acid salts of formula (I).
8. The process of claim 6 , wherein the absorption medium comprises 35 to 45 wt % of amino acid salts of formula (I).
9. The process of claim 6 , wherein the absorption medium comprises at least 40 wt % of water.
10. The process of claim 6 , wherein the gas mixture is a combustion off-gas, a natural gas or a biogas.
11. The process of claim 6 , wherein CO 2 absorbed in the absorption medium is desorbed again by increasing the temperature, reducing the pressure or both and, after this desorption of CO 2 , the absorption medium is used again for absorbing CO 2 .
12. The process of claim 11 , wherein the absorption is carried out at a temperature in the range from 0 to 80° C. and the desorption is carried out at a higher temperature in the range from 50 to 200° C.
13. The process of claim 11 , wherein the absorption is carried out at a pressure in the range from 0.8 to 50 bar and the desorption is carried out at a lower pressure in the range from 0.01 to 10 bar.
14. The process of claim 12 , wherein the absorption is carried out at a temperature in the range from 20 to 70° C. and the desorption is carried out at a higher temperature in the range from 80 to 150° C.
15. The process of claim 12 , wherein desorption is at a temperature at least 30° C. above the temperature during desorption.
16. The process of claim 13 , wherein the absorption is carried out at a pressure in the range from 0.9 to 30 bar and the desorption is carried out at a lower pressure in the range from 0.01 to 10 bar.
17. The process of claim 5 , wherein the gas mixture further comprises SO 2 and, before absorbing CO 2 from the gas mixture, the SO 2 is depleted using a desulfurization process.
18. The process of claim 6 , wherein, before being brought in contact with said absorption medium, the gas mixture has a CO 2 content of 0.1-50% by volume.
19. The process of claim 6 , wherein, before being brought in contact with said absorption medium, the gas mixture has a CO 2 content of 8-20% by volume.