IP Library Granted Patent US 12,359,113
Granted Patent B2
US 12,359,113 · App. 15/995,501 · Granted Jul 15, 2025

Method for dispersing kinetic hydrate inhibitors

Inventors: Jeremy Wayne Bartels (Sugar Land, TX); Regan Andrew Jones (Sugar Land, TX); Kevin Patrick McNamee (Banchory, GB); Thomas M. Weathers, Jr. (Katy, TX)
Assignee: ChampionX LLC
C09K8/524C09K8/52C09K8/54C09K2208/22
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Quick Facts
Patent No.
US 12,359,113
App. No.
15/995,501
Granted
Jul 15, 2025
Kind
B2
Abstract

Methods and dispersing agents for dispersing a polymeric low dose hydrate inhibitor are disclosed. More specifically, the method comprises contacting an aqueous fluid containing a polymeric low dose hydrate inhibitor with a dispersing agent. The dispersing agent can be selected from the group consisting of a C 1 -C 20 alkyl sulfate, a C 10 -C 20 alkyl ether sulfate, a C 10 -C 20 carbonyl sarcosinate, a C 10 -C 20 alkylbenezene sulfonate, a quaternary-ammonium based corrosion inhibitor, a glycol ether, and a combination thereof.

Claims (20)

1. A method for dispersing a polymeric low dose hydrate inhibitor in produced waste water containing the polymeric low dose hydrate inhibitor, the method comprising injecting a dispersing agent into the produced waste water containing the polymeric low dose hydrate inhibitor, and injecting the produced waste water containing the dispersing agent and the polymeric low dose hydrate inhibitor into a well or reservoir, thereby dispersing the polymeric low dose hydrate inhibitor and reducing precipitation of the polymeric low dose hydrate inhibitor, wherein the produced waste water containing the polymeric low dose hydrate inhibitor is present in a separator.

2. The method of claim 1 , wherein the dispersing agent is selected from the group consisting of a C 1 -C 20 alkyl sulfate, a C 10 -C 20 alkyl ether sulfate, a C 10 -C 20 carbonyl sarcosinate, a C 10 -C 20 alkylbenezene sulfonate, a quaternary-ammonium based corrosion inhibitor, a glycol ether, and a combination thereof.

3. The method of claim 2 , wherein the dispersing agent is a C 1 -C 20 alkyl sulfate.

4. The method of claim 3 , wherein the C 1 -C 20 alkyl sulfate has a counter cation selected from the group consisting of sodium, calcium, potassium, magnesium, ammonium, and a combination thereof.

5. The method of claim 4 , wherein the counter cation is selected from the group consisting of sodium, potassium, and a combination thereof.

6. The method of claim 4 , wherein the dispersing agent comprises sodium dodecyl sulfate.

7. The method of claim 2 , wherein the quaternary-ammonium based corrosion inhibitor is selected from the group consisting of benzyl-dimethyl-dodecyl ammonium chloride, benzyl-dimethyl-tetradecyl ammonium chloride, benzyl-dimethyl-hexadecyl ammonium chloride, benzyl-dimethyl-octadecyl ammonium chloride, an alkyl t-butylammonium halide quaternary ammonium salt, and a combination thereof.

8. The method of claim 2 , wherein the glycol ether is selected from the group consisting of diethylene glycol monoethyl ether, ethylene glycol monobutyl ether, and a combination thereof.

9. The method of claim 1 , wherein the polymeric low dose hydrate inhibitor comprises a polymeric kinetic hydrate inhibitor, an anti-agglomerate hydrate inhibitor, or a combination thereof.

10. The method of claim 9 , wherein the polymeric low dose hydrate inhibitor comprises a polymeric kinetic hydrate inhibitor.

11. The method of claim 10 , wherein the polymeric kinetic hydrate inhibitor comprises a homopolymer or a copolymer comprising poly(N-vinyl caprolactam), poly(N-vinyl pyrrolidone), 2-trimethylammoniummethyl methacrylate chloride, 3-dimethylaminopropyl methacrylamide, 2-dimethylaminoethyl methacrylate, N-methyl-N-vinylacetamide, poly(N-isopropyl methacrylamide), poly(N-isopropyl methacrylamide-co-3-trimethylammoniumpropyl methacrylamide chloride), or a combination thereof.

12. The method of claim 11 , wherein the polymeric kinetic hydrate inhibitor comprises a homopolymer or a copolymer comprising poly(N-vinyl caprolactam), poly(N-vinyl pyrrolidone), or a combination thereof.

13. The method of claim 1 , wherein the dispersing agent is injected into the produced waste water the polymeric low dose hydrate inhibitor in the form of a solid or as a solution.

14. The method of claim 13 , wherein the dispersing agent is injected into the produced waste water as a solution.

15. The method of claim 14 , wherein the dispersing agent is injected into the produced waste water at a concentration of from about 0.001 wt. % to about 10 wt. % based on the amount of the polymeric low dose hydrate inhibitor in the waste water.

16. The method of claim 1 , wherein the dispersing agent is injected into the produced waste water containing the polymeric low dose hydrate inhibitor in a batch-wise method.

17. The method of claim 1 , wherein the dispersing agent is injected into the produced waste water containing the polymeric low dose hydrate inhibitor in a metered injection method.

18. The method of claim 1 , wherein the produced waste water is produced from a hydrocarbon extraction and recovery process.

19. A method for dispersing a polymeric low dose hydrate inhibitor in produced waste water containing the polymeric low dose hydrate inhibitor, the method comprising injecting a dispersing agent into the produced waste water containing the polymeric low dose hydrate inhibitor, and injecting the produced waste water containing the dispersing agent and the polymeric low dose hydrate inhibitor into a water disposal well.

20. The method of claim 19 , wherein the dispersing agent is selected from the group consisting of a C 1 -C 20 alkyl sulfate, a C 10 -C 20 alkyl ether sulfate, a C 10 -C 20 carbonyl sarcosinate, a C 10 -C 20 alkylbenezene sulfonate, a quaternary-ammonium based corrosion inhibitor, a glycol ether, and a combination thereof.

Assignments (8)
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 →
CORRECTIVE ASSIGNMENT TO CORRECT THE THE CONVEYING PARTY NAME PREVIOUSLY RECORDED AT REEL: 67104 FRAME: 257. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded May 20, 2024
From: CHAMPIONX USA INC.
To: CHAMPIONX LLC
Reel/Frame 067471/0151 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2024
From: CHAMPION.X USA INC.
To: CHAMPIONX LLC
Reel/Frame 067104/0257 →
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 Sep 22, 2020
From: ECOLAB USA INC.
To: CHAMPIONX USA INC.
Reel/Frame 053849/0537 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 1, 2018
From: BARTELS, JEREMY WAYNE; JONES, REGAN ANDREW; MCNAMEE, KEVIN PATRICK; WEATHERS, THOMAS M., JR.
To: ECOLAB USA INC.
Reel/Frame 045961/0271 →
Continuity (2)
Provisional Application 62514279 · Jun 2, 2017
Related Publication 20180346791A1 · Dec 6, 2018
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