IP Library Granted Patent US 11,332,657
Granted Patent B2
US 11,332,657 · App. 16/753,213 · Granted May 17, 2022

Dual cation hydrate inhibitors

Inventors: Loan Vo (Houston, TX); Deepak S. Monteiro (Houston, TX); Qiang Lan (The Woodlands, TX); Philippe Prince (Pearland, TX)
Assignee: Halliburton Energy Services, Inc.
C09K8/52C07C237/06E21B43/00C09K2208/22
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Quick Facts
Patent No.
US 11,332,657
App. No.
16/753,213
Granted
May 17, 2022
Kind
B2
Abstract

Dual cation hydrate inhibitor compositions and methods of using such compositions to, for example, inhibit the formation of gas hydrate agglomerates are provided. In some embodiments, such methods include introducing a hydrate inhibitor composition into a fluid, wherein the hydrate inhibitor composition includes at least one compound having the structural formula: wherein each of R 1 , R 2 , and R 3 is independently a C 1 to C 6 hydrocarbon chain, wherein R 4 is selected from the group consisting of hydrogen and any C 1 to C 50 hydrocarbon chain, wherein each of R 5 and R 6 is independently selected from the group consisting of hydrogen and a C 1 to C 50 hydrocarbon chain, wherein X − and Y − are counter anions, and wherein each of a and b is independently an integer from 1 to 10.

Claims (39)

1. A method comprising:

introducing a hydrate inhibitor composition into a fluid, wherein the hydrate inhibitor composition comprises at least one compound of the structural formula:

wherein each of R 1 , R 2 , and R 3 is independently a C 1 to C 6 hydrocarbon chain,

wherein R 4 is selected from the group consisting of hydrogen and any C 1 to C 50 hydrocarbon chain,

wherein each of R 5 and R 6 is independently selected from the group consisting of hydrogen and a C 1 to C 50 hydrocarbon chain,

wherein X − and Y − are counter anions, and

wherein each of a and b is independently an integer from 1 to 10.

2. The method of claim 1 wherein X − and Y − are selected from the group consisting of: a carboxylate, a halide, a sulfate, an organic sulfonate, a phosphate, a phosphonate, a hydroxide, and any combination thereof.

3. The method of claim 1 wherein the fluid comprises at least one component selected from the group consisting of: water, a gas, a liquid hydrocarbon, and any combination thereof.

4. The method of claim 1 wherein the hydrate inhibitor composition is introduced into the fluid through a conduit or an injection point in fluid communication with a wellbore in which the fluid resides.

5. The method of claim 1 wherein the hydrate inhibitor composition is introduced into a wellbore penetrating at least a portion of a subterranean formation through which the fluid is flowing.

6. The method of claim 1 wherein the fluid comprises water and has a water cut of up to 80%.

7. The method of claim 1 wherein the hydrate inhibitor composition is introduced into the fluid through an umbilical or a capillary line.

8. The method of claim 1 wherein the fluid comprises water and the hydrate inhibitor composition is introduced into the fluid in an amount such that the compound is present in the fluid in an amount from about 0.1% to about 10% by volume based on the water cut of the fluid.

9. The method of claim 1 wherein each of R 4 and R 5 is a C 1 to C 50 hydrocarbon chain resulting from a reaction between an acrylate or a methacrylate and an amine, the amine being selected from the group consisting of:

a synthetic primary or secondary amine selected from the group consisting of: butylamine, pentylamine, hexylamine, octylamine, dodecylamine, N-methyldodecylamine, N-methyloctylamine, didodecylamine, and any combination thereof;

a primary or secondary fatty amine derived from one or more fatty acids selected from the group consisting of: corn oil, canola oil, coconut oil, safflower oil, sesame oil, palm oil, cottonseed oil, soybean oil, olive oil, sunflower oil, hemp oil, wheat germ oil, tall oil, palm kernel oil, vegetable oil, tallow oil, caprylic acid, capric acid, lauric acid, stearic acid, myristic acid, myristoleic acid, palmitic acid, palmitoleic acid, stearic acid, sapienic acid, elaidic acid, vaccenic acid, linoleic acid, arachidic acid, arachidonic acid, eicosapentaenoic acid, erucic acid, docosahexaenoic acid, behenic acid, lignoceric acid, cerotic acid, oleic acids (cis- and trans-), and any combination thereof; and

any combination thereof.

10. The method of claim 1 wherein the at least one compound is a reaction product of a reaction between (i) an alkylating agent and (ii) a second intermediate resulting from a reaction between a dialkylaminoalkylamine and a first intermediate, the first intermediate resulting from a reaction between an acrylate or a methacrylate and an amine.

11. The method of claim 1 , wherein the fluid resides in a wellbore penetrating at least a portion of a subterranean formation.

12. A method comprising:

introducing a hydrate inhibitor composition into a conduit through which a fluid is flowing, wherein the hydrate inhibitor composition comprises at least one compound of the structural formula:

wherein each of R 1 , R 2 , and R 3 is independently a C 1 to C 6 hydrocarbon chain,

wherein R 4 is selected from the group consisting of hydrogen and any C 1 to C 50 hydrocarbon chain,

wherein each of R 5 and R 6 is independently selected from the group consisting of hydrogen and a C 1 to C 50 hydrocarbon chain,

wherein X − and Y − are counter anions, and

wherein each of a and b is independently an integer from 1 to 10.

13. The method of claim 12 wherein X − and Y − are selected from the group consisting of: a carboxylate, a halide, a sulfate, an organic sulfonate, a phosphate, a phosphonate, a hydroxide, and any combination thereof.

14. The method of claim 12 wherein the fluid comprises at least one component selected from the group consisting of: water, a gas, a liquid hydrocarbon, and any combination thereof.

15. The method of claim 12 wherein the fluid comprises water and has a water cut of up 80%.

16. The method of claim 12 wherein each of R 4 and R 5 is a C 1 to C 50 hydrocarbon chain resulting from a reaction between an acrylate or a methacrylate and an amine, the amine being selected from the group consisting of:

a synthetic primary or secondary amine selected from the group consisting of: butylamine, pentylamine, hexylamine, octylamine, dodecylamine, N-methyldodecylamine, N-methyloctylamine, didodecylamine, and any combination thereof;

a primary or secondary fatty amine derived from one or more fatty acids selected from the group consisting of: corn oil, canola oil, coconut oil, safflower oil, sesame oil, palm oil, cottonseed oil, soybean oil, olive oil, sunflower oil, hemp oil, wheat germ oil, palm kernel oil, vegetable oil, tall oil, tallow oil, caprylic acid, capric acid, lauric acid, stearic acid, myristic acid, myristoleic acid, palmitic acid, palmitoleic acid, stearic acid, sapienic acid, elaidic acid, vaccenic acid, linoleic acid, arachidic acid, arachidonic acid, eicosapentaenoic acid, erucic acid, docosahexaenoic acid, behenic acid, lignoceric acid, cerotic acid, oleic acids (cis- and trans-), and any combination thereof; and

any combination thereof.

17. A method comprising:

introducing a hydrate inhibitor composition into a conduit through which a fluid is flowing, wherein the hydrate inhibitor composition comprises at least one compound of the structural formula:

18. The method of claim 17 wherein the fluid comprises at least one component selected from the group consisting of: water, a gas, a liquid hydrocarbon, and any combination thereof.

19. The method of claim 17 wherein the fluid comprises water and has a water cut of up to 80%.

20. The method of claim 17 wherein the fluid comprises water and the hydrate inhibitor composition is introduced into the fluid in an amount such that the compound is present in the fluid in an amount from about 0.1% to about 10% by volume based on the water cut of the fluid.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2021
From: MULTI-CHEM GROUP, LLC
To: HALLIBURTON ENERGY SERVICES, INC.
Reel/Frame 056681/0849 →
CORRECTIVE ASSIGNMENT TO CORRECT THE 4TH INVENTOR'S NAME PREVIOUSLY RECORDED AT REEL: 52299 FRAME: 058. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Apr 7, 2020
From: VO, LOAN; MONTEIRO, DEEPAK S.; LAN, QIANG; PRINCE, PHILIPPE
To: MULTI-CHEM GROUP, LLC.
Reel/Frame 052327/0527 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 2, 2020
From: VO, LOAN; MONTEIRO, DEEPAK S.; LAN, QIANG; PRINCE, PHILLIPPE
To: MULTI-CHEM GROUP, LLC.
Reel/Frame 052299/0058 →