IP Library Granted Patent US 9,605,196
Granted Patent B2
US 9,605,196 · App. 13/671,374 · Granted Mar 28, 2017

Lubricity agents to increase pump efficiency in hydrate inhibitor applications

Inventors: Paul J. Biggerstaff (Sugar Land, TX); Marc N. Lehmann (Houston, TX); Anna M. Dhuet (Richmond, TX); Jerry J. Weers (Richmond, TX)
Assignee: BAKER HUGHES INCORPORATED
C09K8/52C09K2208/22C09K2208/34
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Quick Facts
Patent No.
US 9,605,196
App. No.
13/671,374
Granted
Mar 28, 2017
Kind
B2
Abstract

Saturated and unsaturated carboxylic fatty acids and alkylamine salts, alkyl esters and alkyl amide derivatives of these fatty acids are effective in improving the lubricity of hydrate inhibitor formulations, thereby effectively reducing the level of wear on moving parts of a pump under a load during pumping of the hydrate inhibitor formulation, for instance into an umbilical for a subsea hydrocarbon production operation.

Claims (36)

1. A method of pumping a hydrate inhibitor composition, the method comprising:

adding to the hydrate inhibitor composition an effective amount to increase lubricity of at least one lubricity agent selected from the group consisting of a C1-C36 carboxylic fatty acid, an alkylamine salt of a C1-C36 fatty acid, an alkyl ester of a C1-C36 fatty acid, an alkylphenol ester of a C1-C36 fatty acid, an alkanolamine salt of a C1-C36 fatty acid, an imidazoline salt of a C1-C36 fatty acid, an anhydride salt of a C1-C36 fatty acid, an alkanol amide of a C1-C36 fatty acid, an alkyl amide of a C1-C36 fatty acid, a polyetheramine salt of a C1-C36 fatty acid, and combinations thereof; and

pumping the hydrate inhibitor composition containing the lubricity agent;

where the hydrate inhibitor composition consists essentially of:

an alcohol hydrate inhibitor selected from the group consisting of methanol, ethanol, monoethylene glycol, triethylene glycol and combinations thereof; and

about 25 ppm to about 20,000 ppm of the lubricity agent;

where the method has an absence of composition vaporization.

2. The method of claim 1 where the fatty acid of the lubricity agent is derived from naturally-occurring fats, naturally-occurring oils, oligomers of naturally-occurring fats, oligomers of naturally-occurring oils, and combinations thereof.

3. The method of claim 1 where the fatty acid is tall oil fatty acid (TOFA).

4. The method of claim 1 where the method further comprises contacting at least one hydrate blockage with the hydrate inhibitor composition to at least partially dissolve the at least one blockage.

5. A method of pumping a hydrate inhibitor composition, the method comprising:

adding to the hydrate inhibitor composition from about 25 ppm to about 20,000 ppm to increase lubricity of at least one lubricity agent selected from the group consisting of a C1-C36 carboxylic fatty acid, an alkyl ester of a C1-C36 fatty acid, an alkylphenol ester of a C1-C36 fatty acid, an anhydride salt of a C1-C36 fatty acid, an alkanol amide of a C1-C36 fatty acid, an alkyl amide of a C1-C36 fatty acid, and combinations thereof;

pumping the hydrate inhibitor composition containing the lubricity agent; and

contacting at least one hydrate blockage with the hydrate inhibitor composition to at least partially dissolve the blockage;

where the hydrate inhibitor composition consists of:

an alcohol hydrate inhibitor selected from the group consisting of methanol, ethanol, monoethylene glycol, triethylene glycol and combinations thereof; and

about 25 ppm to about 20,000 ppm of the lubricity agent;

where the composition has an absence of corrosion inhibitors.

6. The method of claim 5 where the fatty acid of the lubricity agent is derived from naturally-occurring fats, naturally-occurring oils, oligomers of naturally-occurring fats, oligomers of naturally-occurring oils, and combinations thereof.

7. The method of claim 5 where the fatty acid is tall oil fatty acid (TOFA).

8. A method of pumping a hydrate inhibitor composition, the method comprising:

adding to the hydrate inhibitor composition an effective amount to increase lubricity of at least one lubricity agent selected from the group consisting of a C1-C36 carboxylic fatty acid, an alkyl ester of a C1-C36 fatty acid, an alkylphenol ester of a C1-C36 fatty acid, and combinations thereof; and

pumping the hydrate inhibitor composition containing the lubricity agent;

where the hydrate inhibitor composition comprises:

an alcohol hydrate inhibitor selected from the group consisting of methanol, ethanol, monoethylene glycol, triethylene glycol and combinations thereof; and

about 25 ppm to about 500 ppm of the lubricity agent.

9. The method of claim 8 where the at least one lubricity agent is a C1-C36 carboxylic fatty acid.

10. The method of claim 8 where the hydrate inhibitor composition consists essentially of:

an alcohol hydrate inhibitor selected from the group consisting of methanol, ethanol, monoethylene glycol, triethylene glycol and combinations thereof; and

about 25 ppm to about 500 ppm of the lubricity agent.

11. The method of claim 8 where the hydrate inhibitor composition consists of:

an alcohol hydrate inhibitor selected from the group consisting of methanol, ethanol, monoethylene glycol, triethylene glycol and combinations thereof; and

about 25 ppm to about 500 ppm of the lubricity agent.

12. The method of claim 8 where the fatty acid of the lubricity agent is derived from naturally-occurring fats, naturally-occurring oils, oligomers of naturally-occurring fats, oligomers of naturally-occurring oils, and combinations thereof.

13. The method of claim 8 where the fatty acid is tall oil fatty acid (TOFA).

14. The method of claim 8 where the method further comprises contacting at least one hydrate blockage with the hydrate inhibitor composition to at least partially dissolve the at least one blockage.

Assignments (3)
CHANGE OF NAME Recorded Mar 8, 2022
From: BAKER HUGHES, A GE COMPANY, LLC
To: BAKER HUGHES HOLDINGS LLC
Reel/Frame 059339/0098 →
CHANGE OF NAME Recorded Feb 16, 2022
From: BAKER HUGHES INCORPORATED
To: BAKER HUGHES, A GE COMPANY, LLC
Reel/Frame 059126/0311 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 6, 2013
From: BIGGERSTAFF, PAUL J.; LEHMANN, MARC N.; DHUET, ANNA M.; WEERS, JERRY J.
To: BAKER HUGHES INCORPORATED
Reel/Frame 029767/0391 →
Continuity (2)
Provisional Application 61561010 · Nov 17, 2011
Related Publication 20130130941A1 · May 23, 2013