IP Library Granted Patent US 11,752,467
Granted Patent B2
US 11,752,467 · App. 17/227,519 · Granted Sep 12, 2023

Method for removing nitrogen oxides from a gas

Inventor: Jean Francois Granger (Lugano, CH)
Assignee: CASALE SA
B01D53/8628B01D53/90B01D2251/2062B01D2255/504B01D2258/0283
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Quick Facts
Patent No.
US 11,752,467
App. No.
17/227,519
Granted
Sep 12, 2023
Kind
B2
Abstract

A method for removing nitrogen oxides NOx from a gaseous current, comprising the steps of: passing the gaseous current through a de-NOx catalytic bed with iron exchanged zeolite as a catalyst with the addition of ammonia as a reducing agent, wherein the molar ratio of NH3 over NOx is greater than 1.33.

Claims (23)

1. A method for removing nitrogen oxides NOx from a gaseous current, the method comprising:

passing the gaseous current through a first de-NOx catalytic bed and then into a second de-NOx catalytic bed, the second de-NOx catalytic bed including a catalyst that is an iron exchanged zeolite, with an addition of ammonia as a reducing agent;

wherein a molar ratio of NH3 over NOx in the gas admitted to said second de-NOx catalytic bed is 1.4 to 2;

wherein said second de-NOx catalytic bed is operated at a temperature in a range of 420° C. to 435° C.; and

wherein a space velocity in said second de-NOx catalytic bed is 10000 h−1 to 14000 h−1.

2. The method according to claim 1 , wherein said molar ratio of NH3 over NOx is 1.4 to 1.6.

3. The method according to claim 2 , wherein said molar ratio of NH3 over NOx is 1.5.

4. The method according to claim 1 , wherein, after the passage though said second de-NOx catalytic bed, a residual amount of NOx in the gas is not greater than 100 ppm.

5. The method according to claim 1 , wherein, after the passage though said second de-NOx catalytic bed, a residual amount of NOx in the gas is not greater than 50 ppm.

6. The method according to claim 1 , wherein, after the passage though said second de-NOx catalytic bed, a residual amount of NOx in the gas is not greater than 25 ppm.

7. The method according to claim 1 , wherein the temperature at which said second de-NOx catalytic bed is operated is 430° C.

8. The method according to claim 1 , wherein the iron exchanged zeolite catalyst includes MFI, BEA, FER, MOR, FAU, MEL, or combinations thereof.

9. The method according to claim 1 , wherein the iron exchanged zeolite includes an Fe-ZSM-5 type iron exchanged zeolite.

10. The method according to claim 1 , wherein the space velocity in said second de-NOx catalytic bed is 13000 h−1.

11. The method according to claim 1 , wherein the gas in said second de-NOx catalytic bed exhibits an absolute pressure of greater than 1 bar.

12. The method according to claim 11 , wherein the absolute pressure is 2 bar to 25 bar.

13. The method according to claim 11 , wherein the absolute pressure is 5 bar to 15 bar.

14. The method according to claim 11 , wherein the gaseous current is a flue gas of a combustion process, or a tail gas of a process for making nitric acid withdrawn from an absorption column.

15. The method according to claim 1 wherein the gaseous current is a tail gas of a process for making nitric acid, withdrawn from an absorption column.

16. The method according to claim 1 , further comprising:

adding ammonia as a reducing agent to the effluent of said first de-NOx catalytic bed until the molar ratio of NH3 over NOx in said effluent gas is 1.4 to 2; and

passing the effluent gas and ammonia directly through said de-NOx catalytic bed.

17. The method according to claim 16 wherein adding ammonia as a reducing agent to the effluent of said first de-NOx catalytic bed until the molar ratio of NH3 over NOx in said effluent gas is 1.4 to 2 includes adding ammonia as the reducing agent to the effluent of said first de-NOx catalytic bed until the molar ratio of NH3 over NOx in said effluent gas is 1.4 to 1.6.

Priority Claims (2)
WO PCT/EP2016/076152 · Oct 28, 2016 · international
EP 17168721 · Apr 28, 2017 · regional
Continuity (2)
Continuation 16344128
Related Publication 20210229035A1 · Jul 29, 2021