IP Library Granted Patent US 9,884,286
Granted Patent B2
US 9,884,286 · App. 14/949,524 · Granted Feb 6, 2018

Method and system for controlling mercury emissions from coal-fired thermal processes

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Quick Facts
Patent No.
US 9,884,286
App. No.
14/949,524
Granted
Feb 6, 2018
Kind
B2
Abstract

The present disclosure is directed to the use of elemental or speciated iodine and bromine to control total mercury emissions.

Claims (76)

1. A method, comprising:

providing a mercury-containing gas stream comprising vapor-phase mercury, a vapor-phase halogen, and ash particulates;

introducing a reactive surface agent into the mercury-containing gas stream to form particulates comprising at least part of the vapor-phase mercury and the reactive surface agent; and

thereafter removing particulates from the mercury-containing gas stream to form a treated stream, at least a portion of the vapor-phase mercury being removed from the mercury-containing gas stream with removal of the particulates, wherein at least one of the following is true:

(i) the mercury-containing gas stream comprises about 3.5 ppmw or less vapor-phase halogen comprising bromine, iodine, or a mixture thereof;

(ii) in the mercury-containing gas stream, a molar ratio of the vapor-phase halogen to vapor-phase mercury is no more than about 600;

(iii) at an air preheater outlet, a concentration of the vapor-phase halogen ranges from about 0.1 to about 10 ppmw; and

(iv) a concentration of the halogen is about 30 ppmw or less relative to a weight of a mercury-containing feed material that is combusted to produce the vapor-phase mercury.

2. The method of claim 1 , wherein (i) is true and wherein the vapor-phase halogen comprises bromine.

3. The method of claim 1 , wherein (ii) is true and wherein the vapor-phase halogen comprises iodine.

4. The method of claim 1 , wherein (iii) is true and wherein the reactive surface agent is activated carbon.

5. The method of claim 1 , wherein (iv) is true and wherein the mercury-containing gas stream is derived from combusting coal.

6. The method of claim 5 , wherein the coal is contacted with a halogen-containing additive prior to combustion and wherein at least one of the following is true:

(a) the concentration of the halogen in the halogen-containing additive relative to the weight of the coal is less than 30 ppm;

(b) the concentration of the halogen in the halogen-containing additive relative to the weight of the coal is less than 20 ppm; and

(c) the concentration of the halogen in the halogen-containing additive relative to the weight of the coal is less than 10 ppm.

7. The method of claim 1 , wherein the reactive surface agent comprises activated carbon, wherein the removed particulates comprise the ash particulates, the activated carbon and at least part of the vapor-phase mercury and wherein the mercury-containing gas stream is derived from combustion of coal.

8. The method of claim 1 , wherein the vapor-phase halogen is introduced into vapor-phase mercury upstream of an air preheater and wherein the particulate activated carbon is introduced into the mercury-containing gas stream at a location where a temperature of the gas stream ranges from about 150 to about 700° C.

9. The method of claim 1 , wherein the reactive surface agent is introduced by a dry scrubber and wherein the dry scrubber is located upstream of a particulate removal device.

10. The method of claim 1 , wherein the vapor-phase halogen comprises vapor phase iodine and wherein the vapor phase iodine comprises a hydrogen-iodine species and diatomic iodide, and wherein a molecular ratio of the diatomic iodide to the hydrogen-iodine species is at least about 10:1.

11. The method of claim 1 , wherein the mercury-containing gas stream is derived from coal combustion, the coal comprises no more than about 30% unburned carbons, the reactive surface agent is introduced into the mercury-containing gas stream after coal combustion and further comprises one or more of a zeolite, silica, silica alumina, alumina, gamma-alumina, activated alumina, acidified alumina, amorphous aluminosilicate, crystalline aluminosilicate, amorphous silica alumina, ion exchange resin, clay, a transition metal sulfate, porous ceramic, unburned carbon, charcoal, char, coke, carbon black, trona, alkali metal bicarbonate, alkali metal bisulfate, alkali metal bisulfite, alkali metal sulfide, elemental sulfur, limestone, hydrated lime, slaked lime, circulating fluidized bed ash, fluidized catalytic cracker (FCC) fines, fumed silicate, metal oxide particles, and mixtures thereof, and mean, median, and P 90 sizes of the reactive surface agent are no more than about 100 microns.

12. The method of claim 1 , wherein the reactive surface agent is introduced into the mercury-containing gas stream upstream of an air preheater and at a location where a temperature of the gas stream ranges from about 400 to about 700° C.

13. The method of claim 1 , wherein a P 85 size of the reactive surface agent is in the range of from about 1 mm to about 2.5 mm in size and an average diameter of the reactive surface agent is between about 0.75 to about 1.25 mm.

14. The method of claim 1 , wherein the reactive surface agent has a surface area of at least about 500 but no more than about 2,500 m 2 /g and wherein the reactive surface agent has an ash content in the range of from about 10 to about 95%.

15. A method, comprising:

providing a mercury-containing gas stream comprising vapor-phase mercury and a vapor-phase halogen comprising one of bromine, iodine, or a mixture thereof;

introducing a particulate reactive surface agent comprising activated carbon into the mercury-containing gas stream wherein the particulate reactive surface agent is introduced into the mercury-containing gas stream at a location where a temperature of the gas stream ranges from about 150 to about 700° C. to form particulates comprising at least part of the vapor-phase mercury; and

removing the particulates from the mercury-containing gas stream,

wherein at least one of the following is true:

(i) the particulate reactive surface agent further comprises one or more of activated alumina, ceramic, clay, silica, silica-alumina, silicates, zeolites, fine fraction fly ash, FCC fines, and fluidized bed combustor ash;

(ii) the particulate reactive surface agent further comprises at least one porous carbonaceous material selected from the group consisting of charcoal, coke, fly ash, bottom ash, carbon black, activated pet coke, and mixtures thereof, a P 85 size of the particulate reactive surface agent is no more than about 2.5 mm, and an average diameter of the particulate reactive surface agent is between about 0.10 and about 1.25 mm;

(iii) the particulate reactive surface agent further comprises at least one porous carbonaceous material selected from the group consisting of charcoal, coke, fly ash, bottom ash, carbon black, activated pet coke, and mixtures thereof, a surface area of the particulate reactive surface agent is at least about 500 m 2 /g but no more than about 2,500 m 2 /g, and an ash content of the particulate reactive surface agent is in the range of from about 10% to about 95%;

(iv) the particulate reactive surface agent is introduced into the mercury-containing gas stream downstream of an economizer; and

(v) at least a portion of the vapor-phase mercury collects on and is removed with the particulate reactive surface agent.

16. The method of claim 15 , wherein the mercury-containing gas stream is derived from coal combustion, the coal comprises no more than about 30% unburned carbons, the particulate reactive surface agent is introduced into the mercury-containing gas stream after coal combustion and further comprises one or more of a zeolite, silica, silica alumina, alumina, gamma-alumina, activated alumina, acidified alumina, amorphous aluminosilicate, crystalline aluminosilicate, amorphous silica alumina, ion exchange resin, clay, a transition metal sulfate, porous ceramic, unburned carbon, charcoal, char, coke, carbon black, trona, alkali metal bicarbonate, alkali metal bisulfate, alkali metal bisulfate, alkali metal sulfide, elemental sulfur, limestone, hydrated lime, slaked lime, circulating fluidized bed ash, fluidized catalytic cracker (FCC) fines, fumed silicate, metal oxide particles, and mixtures thereof, and mean, median, and P 90 sizes of the particulate reactive surface agent are no more than about 100 microns.

17. The method of claim 15 , wherein the particulate reactive surface agent is introduced into the mercury-containing gas stream upstream of an air preheater and at a location where a temperature of the gas stream ranges from about 400 to about 700° C.

18. The method of claim 15 , wherein (i) is true and wherein the vapor-phase halogen is iodine.

19. The method of claim 18 , wherein the vapor-phase iodine comprises a hydrogen-iodine species and diatomic iodide, and wherein a molecular ratio of the diatomic iodide to the hydrogen-iodine species is at least about 10:1.

20. The method of claim 15 , wherein (ii) is true and wherein the vapor-phase halogen is bromine.

21. The method of claim 15 , wherein (iii) is true and wherein the vapor-phase halogen is iodine and wherein at least one of the following is true:

(i) the mercury-containing gas stream comprises about 3.5 ppmw or less vapor-phase iodine;

(ii) in the mercury-containing gas stream, a molar ratio of vapor-phase iodine to vapor-phase mercury is no more than about 600;

(iii) at an air preheater outlet, a concentration of vapor-phase iodine ranges from about 0.1 to about 10 ppmw;

(iv) a concentration of the iodine is about 30 ppmw or less relative to a weight of a mercury-containing feed material that is combusted to produce the vapor-phase mercury.

22. The method of claim 15 , wherein (iv) is true and wherein a P 85 size of the particulate reactive surface agent is in the range of from about 1 mm to about 2.5 mm in size and an average diameter of the particulate reactive surface agent is between about 0.75 to about 1.25 mm.

23. The method of claim 15 , wherein (v) is true and wherein the particulate reactive surface agent has a surface area of at least about 500 but no more than about 2,500 m 2 /g and wherein the particulate reactive surface agent has an ash content in the range of from about 10 to about 95%.

24. The method of claim 15 , wherein the mercury-containing gas stream is derived from combustion of coal, wherein the coal is contacted with a halogen-containing additive prior to combustion, and wherein at least one of the following is true:

(a) the concentration of the halogen in the halogen-containing additive relative to the weight of the coal is less than 30 ppm;

(b) the concentration of the halogen in the halogen-containing additive relative to the weight of the coal is less than 20 ppm; and

(c) the concentration of the halogen in the halogen-containing additive relative to the weight of the coal is less than 10 ppm.

25. The method of claim 15 , wherein the removed particulates further comprise ash particulates and activated carbon.

26. The method of claim 15 , wherein the vapor-phase halogen is introduced into the vapor-phase mercury upstream of an air preheater.

27. The method of claim 15 , wherein the reactive surface agent is introduced by a dry scrubber and wherein the dry scrubber is located upstream of a particulate removal device.

28. A method, comprising:

combusting, in a thermal unit, a halogen-containing additive and a mercury-containing coal feed material to form a mercury-containing gas stream comprising vapor-phase mercury, a vapor-phase halogen, and ash particulates, wherein the vapor-phase halogen comprises one of vapor-phase bromine, vapor-phrase iodine, or a mixture thereof;

introducing particulate activated carbon into the mercury-containing gas stream to form particulates comprising at least part of the vapor-phase mercury; and

removing the particulates form the mercury-containing gas stream.

29. The method of claim 28 , wherein the vapor-phase halogen comprises vapor-phase bromine.

30. The method of claim 28 , wherein the vapor-phase halogen comprises vapor-phase iodine.

31. The method of claim 30 , wherein the vapor phase iodine comprises a hydrogen-iodine species and diatomic iodide, and wherein a molecular ratio of the diatomic iodide to the hydrogen-iodine species is at least about 10:1.

32. The method of claim 28 , wherein the halogen-containing additive is contacted with the mercury-containing coal feed material prior to combustion and at least one of the following is true:

(a) the concentration of the halogen in the halogen-containing additive relative to the weight of the coal is no more than 30 ppm;

(b) the concentration of the halogen in the halogen-containing additive relative to the weight of the coal is no more than 20 ppm; and

(c) the concentration of the halogen in the halogen-containing additive relative to the weight of the coal is no more than 10 ppm.

33. The method of claim 28 , wherein the vapor-phase halogen is introduced into the mercury-containing gas stream upstream of an air preheater and wherein the particulate activated carbon is introduced into the mercury-containing gas stream at a location where a temperature of the gas stream ranges from about 150 to about 700° C.

34. The method of claim 28 , wherein the vapor-phase halogen is iodine and wherein at least one of the following is true:

(i) the mercury-containing gas stream comprises about 3.5 ppmw or less vapor-phase iodine;

(ii) in the mercury-containing gas stream, a molar ratio of vapor-phase iodine to vapor-phase mercury is no more than about 600;

(iii) at an air preheater outlet, a concentration of vapor-phase iodine ranges from about 0.1 to about 10 ppmw;

(iv) a concentration of the iodine is about 30 ppmw or less relative to a weight of a mercury-containing feed material that is combusted to produce the vapor-phase mercury.

35. The method of claim 28 , wherein a P 85 size of the particulate activated carbon is in the range of from about 1 mm to about 2.5 mm in size and an average diameter of the particulate activated carbon is between about 0.75 to about 1.25 mm.

36. The method of claim 28 , wherein the particulate activated carbon has a surface area of at least about 500 but no more than about 2,500 m 2 /g and wherein the particulate activated carbon has an ash content in the range of from about 10 to about 95%.

37. The method of claim 28 , wherein the particulate activated carbon is introduced into the mercury-containing gas stream at a location where a temperature of the gas stream ranges from about 400 to about 700° C.

38. The method of claim 28 , wherein the removed particulates further comprise ash particulates and activated carbon.

39. The method of claim 28 , wherein the activated carbon is introduced by a dry scrubber and wherein the dry scrubber is located upstream of a particulate removal device.

40. The method of claim 28 , wherein the coal comprises no more than about 30% unburned carbons, the particulate reactive surface agent is introduced into the mercury-containing gas stream after coal combustion and further comprises one or more of a zeolite, silica, silica alumina, alumina, gamma-alumina, activated alumina, acidified alumina, amorphous aluminosilicate, crystalline aluminosilicate, amorphous silica alumina, ion exchange resin, clay, a transition metal sulfate, porous ceramic, unburned carbon, charcoal, char, coke, carbon black, trona, alkali metal bicarbonate, alkali metal bisulfate, alkali metal bisulfite, alkali metal sulfide, elemental sulfur, limestone, hydrated lime, slaked lime, circulating fluidized bed ash, fluidized catalytic cracker (FCC) fines, fumed silicate, metal oxide particles, and mixtures thereof, and mean, median, and P 90 sizes of the particulate reactive surface agent are no more than about 100 microns.

Assignments (8)
SECURITY INTEREST Recorded Jan 3, 2025
From: ARQ SOLUTIONS, LLC; ARQ SOLUTIONS (ES), INC.
To: MIDCAP FUNDING IV TRUST
Reel/Frame 069817/0645 →
RELEASE OF SECURITY INTEREST Recorded Dec 27, 2024
From: CF GLOBAL CREDIT, LP, AS ADMINISTRATIVE AGENT
To: ARQ SOLUTIONS, LLC (F/K/A ADA CARBON SOLUTIONS, LLC); ARQ SOLUTIONS (ES), INC. (F/K/A ADA-ES, INC.)
Reel/Frame 069791/0980 →
CHANGE OF NAME Recorded Feb 21, 2024
From: ADA-ES, INC.
To: ARQ SOLUTIONS (ES), INC.
Reel/Frame 066643/0579 →
PATENT SECURITY AGREEMENT Recorded Feb 1, 2023
From: ADA CARBON SOLUTIONS, LLC; ADA-ES, INC.
To: CF GLOBAL CREDIT, LP
Reel/Frame 062622/0051 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded Jun 4, 2021
From: THE BANK OF NEW YORK MELLON, AS ADMINISTRATIVE AGENT
To: ADA-ES, INC.
Reel/Frame 056483/0657 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2019
From: FRENCH, NINA B.; DURHAM, MICHAEL D.; BALDREY, KENNETH E.; BISQUE, RAMON E.
To: ADA-ES, INC.
Reel/Frame 050657/0448 →
NOTICE OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Dec 7, 2018
From: ADA-ES, INC.
To: THE BANK OF NEW YORK MELLON, AS ADMINISTRATIVE AGENT
Reel/Frame 047742/0652 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 23, 2015
From: SJOSTROM, SHARON; SENIOR, CONNIE; LAGARENNE, JON
To: ADA-ES, INC.
Reel/Frame 037122/0677 →