IP Library Granted Patent US 8,632,742
Granted Patent B2
US 8,632,742 · App. 13/657,484 · Granted Jan 21, 2014

Methods of controlling mercury emission

Inventors: Bruce A. Keiser (Plainfield, IL); Jitendra Shah (Naperville, IL); John V. Meier (Chicago, IL); Robert W. Dorner (Naperville, IL); Jianwei Yuan (Aurora, IL); Rebecca L. Stiles (Naperville, IL); Wayne Carlson (Batavia, IL); Darlington Mlambo (Naperville, IL)
Assignee: Nalco Company
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Quick Facts
Patent No.
US 8,632,742
App. No.
13/657,484
Granted
Jan 21, 2014
Kind
B2
Abstract

Disclosed are methods for controlling, mercury emissions, and more particularly, to methods for controlling mercury re-emissions from a wet flue gas desulfurizer used in a combustion process. A method of controlling mercury re-emission from a combustion process includes measuring either mercury concentration, oxidation-reduction, potential (ORP), and/or sulfide concentration within a scrubber liquor of a wet flue gas desulpherizer (wFGD); correlating the mercury concentration, ORP, and /or sulfide concentration with an amount of mercury re-emission additive required in the scrubber liquor to reduce and/or prevent mercury re-emission to a selected level; and adjusting the rate of addition of mercury re-emission additive into the scrubber liquor to attain the selected level of mercury re-emission.

Claims (32)

1. A method of controlling mercury re-emission from a combustion process, the method comprising:

(a) measuring either mercury concentration, oxidation-reduction potential (ORP), and/or sulfide concentration within a scrubber liquor of a wet flue gas desulpherizer (wFGD);

(b) correlating the mercury concentration, ORP, and/or sulfide concentration with an amount of mercury re-emission additive required in the scrubber liquor to reduce and/or prevent mercury re-emission to a selected level; and

(c) adjusting the rate of addition of mercury re-emission additive into the scrubber liquor to attain the selected level of mercury re-emission.

2. The method of claim 1 , wherein mercury concentration is measured.

3. The method of claim 1 , wherein oxidation-reduction potential is measured.

4. The method of claim 1 , wherein sulfide concentration is measured.

5. The method of claim 1 , wherein the rate of addition of mercury re-emission control additive is adjusted to reduced the scrubber liquor ionic mercury concentration to less than 500 ppt.

6. The method of claim 1 , wherein the rate of addition of mercury re-emission control additive is adjusted to reduce the scrubber liquor ionic mercury concentration to less than 200 ppt.

7. The method of claim 1 , wherein the rate of addition of mercury re-emission control additive is adjusted to reduce the scrubber liquor ionic mercury concentration to less than 200 ppt and the percent mercury re-emission from the scrubber liquor is reduced to 10% or less.

8. The method of claim 1 , wherein the rate of addition of mercury re-emission control additive is adjusted to reduce the scrubber liquor mercury concentration to less than 100 ppt and the percent mercury re-emission from the scrubber liquor is reduced to 1% or less.

9. The method of claim 1 , wherein the ORP value is measured, and the rate of addition of mercury re-emission control additive is adjusted to reduce the scrubber liquor oxidation-reduction potential by 100 mV.

10. The method of claim 1 , wherein the ORP value is measured, and the rate of addition of mercury re-emission control additive is adjusted to reduce the scrubber liquor oxidation-reduction potential by 300 mV.

11. The method of claim 1 , wherein the ORP value is measured, and the rate of addition of mercury re-emission control additive is adjusted to reduce the scrubber liquor oxidation-reduction potential by 400 mV.

12. The method of claim 1 , wherein the oxidation-reduction potential of the scrubber liquor is measured prior to adjusting the rate of addition of mercury re-emission control additive to provide a baseline, wherein the rate of addition of mercury re-emission is control additive is thereafter increased to reduce the scrubber liquor oxidation-reduction potential by 50-400 mV.

13. The method of claim 12 , wherein the reduction of the scrubber liquor oxidation-reduction potential by 50-400 mV correlates to a decrease in mercury re-emission from the scrubber liquor to a value of 20% mercury re-emission or less.

14. The method of claim 12 , wherein the reduction of the scrubber liquor oxidation-reduction potential by 50-400 mV correlates to a decrease in mercury re-emission from the scrubber liquor to a value of 10% mercury re-emission or less.

15. The method of claim 12 , wherein the reduction of the scrubber liquor oxidation-reduction potential by 50-400 mV correlates to a decrease in mercury re-emission from the scrubber liquor to a value of 1% mercury re-emission or less.

16. The method of claim 1 , wherein the rate of addition of mercury re-emission control additive is adjusted to increase the scrubber liquor sulfide concentration to greater than 20 ppm.

17. The method of claim 1 , wherein the rate of addition of mercury re-emission control additive is adjusted to increase the scrubber liquor sulfide concentration to greater than 50 ppm.

18. The method of claim 1 , wherein the rate of addition of mercury re-emission control additive is adjusted to increase the scrubber liquor sulfide concentration to greater than 70 ppm.

19. The method of claim 1 , wherein the rate of addition of mercury re-emission control additive is adjusted to increase the scrubber liquor sulfide concentration to a range of about 20 ppm to about 100 ppm.

20. The method of claim 1 , wherein the rate of addition of mercury re-emission control additive is adjusted to increase the scrubber liquor sulfide concentration to a range of about 30 ppm to about 70 ppm.

21. The method of claim 1 , wherein the mercury re-emission control additive is a polydithiocarbamic compound.

22. The method of claim 1 , wherein the mercury re-emission control additive is an ethylene dichloride ammonia polymer containing from 5 to 55 mole % of dithiocarbamate salt groups.

23. The method of claim 1 , wherein the mercury re-emission control additive is a polymer derived from at least two monomers: acrylic-x and an alkylamine, wherein said acrylic-x has the following formula:

wherein X═OR, OH and salts thereof, or NHR 2 and wherein R 1 and R 2 is H or an alkyl or aryl group, wherein R is an alkyl or aryl group, wherein the molecular weight of said polymer is between 500 to 200,000, and wherein said polymer is modified to contain a functional group capable of scavenging one or more compositions containing one or more metals.

24. The method of claim 23 , wherein the functional group capable of scavenging one or more compositions containing one or more metals is a sulfur containing functional group.

25. The method of claim 1 , wherein the mercury re-emission control additive is selected from the group consisting of: a poly-dithiocarbamic compound, sodium sulfide, sodium hydrosulfide, sodium bisulfide, a poly-sulfide, diethyldithiocarbamate or a sodium salt thereof, dimethyldithiocarbamate or a sodium salt thereof, an inorganic poly-sulfide or blend, a sodium or calcium salt of 1,3,5-triazine-2,4,6(1H,3H,5H)-trithione, an activated carbon, 2,3-dimercaptopropanol, dimercaptosuccinic acid, 1,8-octanedithiol, 1,2-dithiolane-3-valeric acid, 2-methyl 1,3-dithiolane, and mercaptoacetic acid or a sodium salt thereof.

26. The method of claim 1 , wherein at least one of measurement of ionic mercury concentration, oxidation-reduction potential, and sulfide ion concentration is automated.

27. The method of claim 1 , wherein adjustment of the rate of addition of mercury re-emission control additive is automatic in response to a measurement of at least one of the ionic mercury concentration, the oxidation-reduction potential, and the sulfide ion concentration.

28. The method of claim 1 , wherein at least one of mercury concentration, oxidation-reduction potential, and sulfide ion concentration are continuously monitored.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2017
From: NALCO COMPANY LLC
To: ECOLAB USA INC.
Reel/Frame 043134/0052 →
CHANGE OF NAME Recorded Jun 20, 2017
From: NALCO COMPANY
To: NALCO COMPANY LLC
Reel/Frame 042914/0827 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2012
From: KEISER, BRUCE A.; SHAH, JITENDRA; MEIER, JOHN V.; DORNER, ROBERT W.; YUAN, JIANWEI; STILES, REBECCA L.; CARLSON, WAYNE; MLAMBO, DARLINGTON
To: NALCO COMPANY
Reel/Frame 029168/0966 →
Continuity (6)
Continuation In Part 13366441 · Feb 6, 2012
Continuation In Part 13366461 · Feb 6, 2012
Continuation In Part 13366610 · Feb 6, 2012
Continuation In Part 13366630 · Feb 6, 2012
Continuation In Part 11952637 · Dec 7, 2007
Related Publication 20130180923A1 · Jul 18, 2013