IP Library Granted Patent US 10,018,017
Granted Patent B2
US 10,018,017 · App. 14/802,725 · Granted Jul 10, 2018

Low dosage kinetic hydrate inhibitors for natural gas production systems

Inventors: Howard James Spencer (Liverpool, GB); Ravinder Virdee (Liverpool, GB); Michael P. Squicciarini (Richmond, TX); Gordon T. Rivers (Houston, TX); Marc N. Lehmann (Houston, TX)
Assignee: Baker Hughes, a GE company, LLC
E21B37/06C08F220/34C08F226/06C09K8/52C10L3/107C09K2208/22
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,018,017
App. No.
14/802,725
Granted
Jul 10, 2018
Kind
B2
Abstract

Copolymers containing acryloylmorpholine and vinylimidazole, and optionally vinylcaprolactam and/or n-vinyl pyrrolidone, have shown superior results in hydrate inhibition tests at conditions of 7° C. subcooling dosed at 1 vol % based on the water cut of the system fluids. The copolymer product has also passed high TDS (total dissolved solids) brine compatibility tests and secondary property tests including foaming and hot injection tests which make it useful as a kinetic hydrate inhibitor in gas production systems susceptible to the formation of natural gas hydrates.

Claims (41)

1. A method for inhibiting formation of hydrates consisting essentially of contacting a fluid including water and hydrate-forming guest molecules that form hydrates at hydrate forming conditions, with an amount of a kinetic hydrate inhibitor (KHI) effective for inhibiting hydrate formation at the hydrate forming conditions, where the KHI is selected from the group consisting of:

a copolymer comprising monomers selected from the group consisting of acryloylmorpholine, vinylimidazole, n-vinyl pyrrolidone and combinations thereof; and

a terpolymer selected from the group consisting of:

acryloylmorpholine, vinylimidazole, and vinylcaprolactam monomers,

vinylimidazole, vinylcaprolactam, and n-vinyl pyrrolidone monomers, and

acryloylmorpholine, vinylimidazole, and n-vinyl pyrrolidone monomers.

2. The method of claim 1 where:

in case the KHI is a copolymer it is a copolymer of acryloylmorpholine and vinylimidazole, and

in case the KHI is a terpolymer it is a terpolymer of acryloylmorpholine, vinylimidazole and vinylcaprolactam.

3. The method of claim 2 where:

in case of the copolymer of acryloylmorpholine and vinylimidazole, the molar ratio of acryloylmorpholine to vinylimidazole ranges from about 1:99 to about 99:1; and

in case of the terpolymer of acryloylmorpholine, vinylimidazole and vinylcaprolactam, the molar ratio of acryloylmorpholine to vinylimidazole to vinylcaprolactam ranges from about 1:1:98 to about 1:98:1 to about 98:1:1.

4. The method of claim 1 where the effective amount of the KHI in the fluid ranges from about 1 to about 15 vol % based on the water in the fluid.

5. The method of claim 1 where the fluid is present in a wellbore, a pipeline, an umbilical, a pipe, a transfer line, a valve, a slug catcher, and combinations thereof.

6. The method of claim 1 where the water is brine.

7. A method for inhibiting formation of hydrates consisting essentially of contacting a fluid including brine and hydrate-forming guest molecules that form hydrates at hydrate forming conditions, with from about 1 to about 15 vol % based on the water in the fluid of a kinetic hydrate inhibitor (KHI) effective for inhibiting hydrate formation at the hydrate forming conditions, where the KHI is selected from the group consisting of:

a copolymer comprising monomers selected from the group consisting of acryloylmorpholine, vinylimidazole, n-vinyl pyrrolidone and combinations thereof; and

a terpolymer selected from the group consisting of:

acryloylmorpholine, vinylimidazole, and vinylcaprolactam monomers,

vinylimidazole, vinylcaprolactam, and n-vinyl pyrrolidone monomers, and

acryloylmorpholine, vinylimidazole, and n-vinyl pyrrolidone monomers.

8. The method of claim 7 where:

in case the KHI is a copolymer it is a copolymer of acryloylmorpholine and vinylimidazole, and

in case the KHI is a terpolymer it is a terpolymer of acryloylmorpholine, vinylimidazole and vinylcaprolactam.

9. The method of claim 8 where:

in case of the copolymer of acryloylmorpholine and vinylimidazole, the molar ratio of acryloylmorpholine to vinylimidazole ranges from about 1:99 to about 99:1; and

in case of the terpolymer of acryloylmorpholine, vinylimidazole and vinylcaprolactam, the molar ratio of acryloylmorpholine to vinylimidazole to vinylcaprolactam ranges from about 1:1:98 to about 1:98:1 to about 98:1:1.

10. The method of claim 7 where the fluid is present in a wellbore, a pipeline, an umbilical, a pipe, a transfer line, a valve, a slug catcher, and combinations thereof.

11. A method for inhibiting formation of hydrates consisting of contacting a fluid including brine and hydrate-forming guest molecules that form hydrates at hydrate forming conditions, with from about 1 to about 15 vol % based on the water in the fluid of a kinetic hydrate inhibitor (KHI) effective for inhibiting hydrate formation at the hydrate forming conditions, where the KHI is selected from the group consisting of:

a copolymer comprising monomers selected from the group consisting of acryloylmorpholine, vinylimidazole, n-vinyl pyrrolidone and combinations thereof; and

a terpolymer selected from the group consisting of:

acryloylmorpholine, vinylimidazole, and vinylcaprolactam monomers,

vinylimidazole, vinylcaprolactam, and n-vinyl pyrrolidone monomers, and

acryloylmorpholine, vinylimidazole, and n-vinyl pyrrolidone monomers.

12. The method of claim 11 where:

in case the KHI is a copolymer it is a copolymer of acryloylmorpholine and vinylimidazole, and

in case the KHI is a terpolymer it is a terpolymer of acryloylmorpholine, vinylimidazole and vinylcaprolactam.

13. The method of claim 12 where:

in case of the copolymer of acryloylmorpholine and vinylimidazole, the molar ratio of acryloylmorpholine to vinylimidazole ranges from about 1:99 to about 99:1; and

in case of the terpolymer of acryloylmorpholine, vinylimidazole and vinylcaprolactam, the molar ratio of acryloylmorpholine to vinylimidazole to vinylcaprolactam ranges from about 1:1:98 to about 1:98:1 to about 98:1:1.

14. The method of claim 11 where the fluid is present in a wellbore, a pipeline, an umbilical, a pipe, a transfer line, a valve, a slug catcher, and combinations thereof.

Assignments (2)
CHANGE OF NAME Recorded Jun 12, 2018
From: BAKER HUGHES INCORPORATED
To: BAKER HUGHES, A GE COMPANY, LLC
Reel/Frame 046350/0385 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 4, 2015
From: SPENCER, HOWARD JAMES; VIRDEE, RAVINDER; SQUICCIARINI, MICHAEL P.; RIVERS, GORDON T.; LEHMANN, MARC N.
To: BAKER HUGHES INCORPORATED
Reel/Frame 036955/0742 →
Continuity (3)
Continuation 13648491 · Oct 10, 2012
Provisional Application 61549576 · Oct 20, 2011
Related Publication 20150322746A1 · Nov 12, 2015