IP Library Granted Patent US 8,048,818
Granted Patent B2
US 8,048,818 · App. 12/055,439 · Granted Nov 1, 2011

In-situ regeneration of a catalyst masked by calcium sulfate

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Quick Facts
Patent No.
US 8,048,818
App. No.
12/055,439
Granted
Nov 1, 2011
Kind
B2
Abstract

An in-situ method for regenerating a deactivated catalyst removes a calcium sulfate layer masking active catalyst sites. A reducing agent converts the calcium sulfate to calcium oxide, which is then removed, by reintrainment into the flue gas steam using soot blowers or sonic horns. The method is particularly useful for regenerating selective catalytic reduction (SCR) catalysts used to remove nitrogen oxides from flue gas produced by combustion of coal from the Powder River Basin. The method can be practiced using existing SCR system hardware, and without removing the SCR system from service.

Claims (41)

1. A method for the regeneration of a selective catalytic reduction catalyst by removing at least one calcium sulfate layer located on the selective catalytic reduction catalyst, the method comprising the steps of:

(i) providing a selective catalytic reduction catalyst having deposited thereon at least one calcium sulfate layer;

(ii) supplying at least one reducing agent to the selective catalytic reduction catalyst, wherein the at least one reducing agent is selected based on its ability to convert the at least one calcium sulfate layer located on the selective catalytic reduction catalyst to at least one calcium oxide layer located on the selective catalytic reduction catalyst;

(iii) contacting the at least one reducing agent with the at least one calcium sulfate layer located on the selective catalytic reduction catalyst in order to convert the at least one calcium sulfate layer to at least one calcium oxide layer; and

(iv) removing the at least one calcium oxide layer from the selective catalytic reduction catalyst,

wherein the selective catalytic reduction catalyst is located in a selective catalytic reduction system during the method, or is located in a selective catalytic reduction system that is in operation during the method, or is utilized in a selective catalytic reduction system after performance of the method.

2. The method of claim 1 , wherein the at least one calcium sulfate layer is contacted with the at least one reducing agent at a temperature greater than about 550° F.

3. The method of claim 1 , wherein the at least one calcium oxide layer is removed by a calcium oxide removal means.

4. The method of claim 1 , wherein the at least one calcium oxide layer on the selective catalytic reduction catalyst is removed by washing with a dilute solution of a weak acid.

5. The method of claim 1 , wherein the at least one reducing agent is a gas.

6. The method of claim 1 , wherein the at least one reducing agent is a straight chain aliphatic hydrocarbon.

7. The method of claim 1 , wherein the at least one reducing agent is selected from methane, hydrogen and carbon monoxide.

8. The method of claim 1 , wherein the at least one calcium sulfate layer is contacted with the at least one reducing agent using hot air as a carrier for the at least one reducing agent.

9. The method of claim 1 , wherein the at least one reducing agent is a liquid.

10. The method of claim 1 , wherein the selective catalytic reduction catalyst is a noble metal catalyst.

11. The method of claim 1 , wherein the selective catalytic reduction catalyst is selected from vanadium, titanium, molybdenum, tungsten and oxides thereof.

12. A method for regenerating a selective catalytic reduction catalyst by removing at least one calcium sulfate layer located on the selective catalytic reduction catalyst, where the selective catalytic reduction catalyst is part of a selective catalytic reduction system designed to remove nitrogen oxides from an exhaust gas of a coal-fired boiler, the method comprising the steps of:

(a) providing a selective catalytic reduction catalyst having deposited thereon at least one calcium sulfate layer;

(b) supplying at least one reducing agent to the selective catalytic reduction catalyst, wherein the at least one reducing agent is selected based on its ability to convert the at least one calcium sulfate layer located on the selective catalytic reduction catalyst to at least one calcium oxide layer located on the selective catalytic reduction catalyst;

(c) contacting the at least one reducing agent with the at least one calcium sulfate layer located on the selective catalytic reduction catalyst in order to convert the at least one calcium sulfate layer to at least one calcium oxide layer; and

(d) removing the at least one calcium oxide layer from the selective catalytic reduction catalyst,

wherein the selective catalytic reduction catalyst is located in a selective catalytic reduction system for a coal-fired boiler during the method, or is utilized in a selective catalytic reduction system for a coal-fired boiler after performance of the method.

13. The method of claim 12 , wherein the at least one calcium sulfate layer is contacted with the at least one reducing agent at a temperature greater than about 550° F.

14. The method of claim 12 , wherein the selective catalytic reduction system has at least one ammonia injection system located upstream of the selective catalytic reduction catalyst, and the at least one reducing agent is introduced through the at least one ammonia injection system.

15. The method of claim 12 , wherein the at least one calcium oxide layer is removed by one of soot blowers and sonic horns.

16. The method of claim 12 , wherein the at least one calcium oxide layer is removed by washing with a dilute solution of a weak acid.

17. The method of claim 12 , wherein the at least one reducing agent is a straight chain aliphatic hydrocarbon.

18. The method of claim 12 , wherein the at least one reducing agent is selected from methane, hydrogen and carbon monoxide.

19. The method of claim 12 , wherein the selective catalytic reduction catalyst is contacted with at least one reducing agent using hot air as a carrier for the at least one reducing agent.

20. The method of claim 12 , wherein the exhaust gas is produced by the combustion of a low sulfur coal.

21. The method of claim 12 , wherein the selective catalytic reduction system is in simultaneous operation to remove nitrogen oxides during the operation of the method of claim 13 .

22. A method for regenerating in-situ a selective catalytic reduction catalyst by removing at least one calcium sulfate layer located on the selective catalytic reduction catalyst, where the in-situ selective catalytic reduction catalyst is part of a selective catalytic reduction system designed to remove nitrogen oxides from an exhaust gas of a coal-fired boiler, the method comprising the steps of:

(I) providing an in-situ selective catalytic reduction catalyst having deposited thereon at least one calcium sulfate layer;

(II) supplying at least one reducing agent to the in-situ selective catalytic reduction catalyst via at least one ammonia injection system of the selective catalytic reduction system that is located upstream thereof, wherein the at least one reducing agent is selected based on its ability to convert the at least one calcium sulfate layer located on the in-situ selective catalytic reduction catalyst to at least one calcium oxide layer located on the in-situ selective catalytic reduction catalyst;

(III) contacting the at least one reducing agent with the at least one calcium sulfate layer located on the in-situ selective catalytic reduction catalyst in order to convert the at least one calcium sulfate layer to at least one calcium oxide layer; and

(IV) removing the at least one calcium oxide layer from the in-situ selective catalytic reduction catalyst via at least one sootblower or sonic horn,

wherein the selective catalytic reduction catalyst is located in a selective catalytic reduction system for a coal-fired boiler during the method and is therefore an in-situ regeneration of a selective catalytic reduction catalyst.

23. The method of claim 22 , wherein the calcium sulfate is contacted with the at least one reducing agent at a temperature greater than about 550° F.

24. The method of claim 22 , wherein the at least one reducing agent is supplied in an amount from about one part per million to about several thousand parts per million.

25. The method of claim 22 , wherein the in-situ selective catalytic reduction catalyst is contacted with the at least one reducing agent for a time from about a few minutes to about a few hours.

26. The method of claim 22 , wherein the selective catalytic reduction system is in simultaneous operation to remove nitrogen oxides during the operation of the method of claim 22 .

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Jul 1, 2021
From: BANK OF AMERICA, N.A.
To: DIAMOND POWER INTERNATIONAL, LLC (F/K/A DIAMOND POWER INTERNATIONAL, INC.); MEGTEC TURBOSONIC TECHNOLOGIES, INC.; THE BABCOCK & WILCOX COMPANY (F/K/A BABCOCK & WILCOX POWER GENERATION GROUP, INC.); BABCOCK & WILCOX SPIG, INC.; BABCOCK & WILCOX TECHNOLOGY, LLC (F/K/A MCDERMOTT TECHNOLOGY, INC.); SOFCO-EFS HOLDINGS LLC; BABCOCK & WILCOX MEGTEC, LLC
Reel/Frame 057337/0823 →
RELEASE OF SECURITY INTEREST Recorded May 17, 2018
From: LIGHTSHIP CAPITAL LLC
To: BABCOCK & WILCOX ENTERPRISES, INC.; THE BABCOCK & WILCOX COMPANY; DIAMOND POWER INTERNATIONAL, LLC; BABCOCK & WILCOX MEGTEC, LLC; MEGTEC TURBOSONIC TECHNOLOGIES, INC.; BABCOCK & WILCOX UNIVERSAL, INC.; BABCOCK & WILCOX TECHNOLOGY, LLC
Reel/Frame 046182/0829 →
SECURITY INTEREST Recorded Aug 10, 2017
From: THE BABCOCK & WILCOX COMPANY; DIAMOND POWER INTERNATIONAL, LLC; BABCOCK & WILCOX MEGTEC, LLC; MEGTEC TURBOSONIC TECHNOLOGIES, INC.; BABCOCK & WILCOX UNIVERSAL, INC.; BABCOCK & WILCOX TECHNOLOGY, LLC
To: LIGHTSHIP CAPITAL LLC
Reel/Frame 043515/0001 →
CHANGE OF NAME Recorded Sep 24, 2015
From: BABCOCK & WILCOX POWER GENERATION GROUP, INC.
To: THE BABCOCK & WILCOX COMPANY
Reel/Frame 036675/0434 →
SECURITY INTEREST Recorded Jul 28, 2015
From: BABCOCK & WILCOX POWER GENERATION GROUP, INC. (TO BE RENAMED THE BABCOCK AND WILCOX COMPANY)
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 036201/0598 →
SECURITY INTEREST Recorded Jul 22, 2014
From: BABCOCK & WILCOX POWER GENERATION GROUP, INC.
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 033380/0744 →