IP Library Granted Patent US 10,308,886
Granted Patent B2
US 10,308,886 · App. 15/135,088 · Granted Jun 4, 2019

Development of a novel high temperature stable scavenger for removal of hydrogen sulfide

Inventors: Geeta Rana (Missouri City, TX); Julian M. Gallardo (Pearland, TX); Matthew Trevino (Houston, TX)
Assignee: ECOLAB USA INC.
C10L3/103B01D53/52B01D53/78C10G29/20C10G29/22C10G29/26C10G75/02B01D53/1468B01D53/1493B01D2252/202B01D2252/205B01D2252/2023B01D2252/20431B01D2252/602B01D2256/24B01D2257/304B01D2257/306C10G2300/207C10G2300/80C10L2290/545
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Quick Facts
Patent No.
US 10,308,886
App. No.
15/135,088
Granted
Jun 4, 2019
Kind
B2
Abstract

The present disclosure provides compositions and methods that are useful in removing, lowering the amount of, or otherwise controlling hydrogen sulfide and mercaptans. The compositions and methods can be used in any industry where hydrogen sulfide poses problems, such as when dealing with crude oil based, natural gas based, and/or coal based products. The present disclosure provides compositions and methods that can reduce the amount of or eliminate hydrogen sulfide in a variety of mediums.

Claims (25)

1. A method of treating hydrogen sulfide in a stream comprising:

adding a composition to a stream comprising an amount of hydrogen sulfide, wherein the composition comprises one or more scavenger compounds having the following general formula:

wherein the C 1 -C 6 ring structure may be aromatic or cyclic aliphatic;

C 1 -C 6 may be independently selected from carbon, nitrogen, oxygen, and sulfur, wherein C 2 may be present or absent and, if absent, the ring structure is a five-membered ring structure;

wherein C 2 -C 4 may be independently selected from the group: X-R-{(OCH 2 ) k OH} m ;

wherein the ring structure may be substituted with an electron withdrawing group or an electron donating group;

X may be selected from the group consisting of carbon, nitrogen, oxygen, sulfur, a carbonyl group, an alkyl group, and an alkenyl group;

R may be selected from the group consisting of hydrogen, an alkyl group, an alkenyl group, an alkynyl group, nitrogen and oxygen, wherein the alkyl group, alkenyl group and the alkynyl group may be unsubstituted or substituted;

k is an integer selected from 0 to 25; and

m is an integer selected from 1 to 4.

2. The method of claim 1 , wherein the ring structure is aromatic, X is N(NH), R is a C 1 -C 8 alkyl group, and k+m=18.

3. The method of claim 1 , wherein the ring structure is aromatic, X is NCH 2 OH, R is a C 1 -C 8 alkyl group, and k+m=7.

4. The method of claim 1 , wherein the stream is a liquid stream or a gaseous stream.

5. The method of claim 1 , wherein the stream comprises one or more hydrocarbons.

6. The method of claim 1 , wherein the composition excludes triazine compounds.

7. The method of claim 1 , wherein the composition comprises a solvent selected from the group consisting of isopropanol, methanol, toluene, water, xylene, ethylene glycols, propylene glycols, and any combination thereof.

8. The method of claim 7 , wherein the solvent comprises from about 10% to about 99%, by weight, of the one or more scavenger compounds.

9. The method of claim 7 , wherein the solvent comprises from about 30% to about 70%, by weight, of the one or more scavenger compounds.

10. The method of claim 1 , wherein the one or more scavengers are thermally stable at a temperature of about 200° C.

11. The method of claim 1 , wherein the composition comprises one or more additives selected from the group consisting of asphaltene inhibitors, paraffin inhibitors, corrosion inhibitors, scale inhibitors, emulsifiers, water clarifiers, dispersants, emulsion breakers, additional hydrogen sulfide scavengers, gas hydrate inhibitors, biocides, pH modifiers, surfactants, solvents, and any combination thereof.

12. The method of claim 1 , wherein the stream is used in the production, transportation, storage, and/or separation of crude oil or natural gas.

13. The method of claim 1 , wherein the stream is used or produced in a coal-fired process, a waste-water process, a farm, a slaughter house, a land-fill, a mining operation, a pulp and paper facility, or a biofuel process.

14. The method of claim 1 , wherein the method lowers the amount of hydrogen sulfide in the stream by about 85% to about 100%.

15. The method of claim 1 , wherein a ratio of an amount of the one or more scavenger compounds added to the stream to the amount of hydrogen sulfide is from about 1:1 to about 30:1.

16. The method of claim 1 , wherein the one or more scavenger compounds are non-corrosive.

Assignments (9)
RELEASE OF SECURITY INTEREST IN PATENTS Recorded Jul 17, 2025
From: JPMORGAN CHASE BANK, N.A.
To: CHAMPIONX LLC; APERGY ESP SYSTEMS, LLC; APERGY BMCS ACQUISITION CORP; HARBISON-FISCHER, INC.; NORRIS RODS, INC.,; NORRIS RODS, INC.,; NORRISEAL-WELLMARK, INC.; PCS FERGUSON, INC.; QUARTZDYNE, INC.; US SYNTHETIC CORPORATION
Reel/Frame 072004/0019 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 7, 2023
From: CHAMPIONX USA INC.
To: CHAMPIONX LLC
Reel/Frame 065799/0403 →
RELEASE OF SECURITY INTEREST Recorded Jun 7, 2022
From: BANK OF AMERICA, N.A.
To: CHAMPIONX USA INC.
Reel/Frame 060304/0267 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2020
From: ECOLAB USA INC.
To: CHAMPIONX USA INC.
Reel/Frame 053624/0124 →
SECURITY INTEREST Recorded Jun 5, 2020
From: CHAMPIONX USA INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 052848/0368 →
SECURITY INTEREST Recorded Jun 5, 2020
From: CHAMPIONX USA INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 053250/0001 →
ANNUAL RENEWAL SHOWING ADDRESS CHANGE Recorded Jan 4, 2019
From: ECOLAB USA INC.
To: ECOLAB USA INC.
Reel/Frame 048645/0082 →
CORRECTIVE ASSIGNMENT TO CORRECT THE NAME OF ASSIGNEE PREVIOUSLY RECORDED ON REEL 038356 FRAME 0883. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Apr 27, 2016
From: RANA, GEETA; GALLARDO, JULIAN M., III; TREVINO, MATTHEW
To: ECOLAB USA INC.
Reel/Frame 038534/0417 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2016
From: RANA, GEETA; GALLARDO, JULIAN M., III; TREVINO, MATTHEW
To: ECOLA USA INC.
Reel/Frame 038356/0883 →
Continuity (2)
Provisional Application 62151083 · Apr 22, 2015
Related Publication 20160312141A1 · Oct 27, 2016
Cited By (2)
US 12,195,371 US 12,312,291