Succinimide-based copolymers and use as hydrate inhibitors

Patent metadata

Field	Value
Publication number	US-11060042-B2
Application number	US-201916728245-A
Country	US
Kind code	B2
Filing date	Dec 27, 2019
Priority date	May 6, 2016
Publication date	Jul 13, 2021
Grant date	Jul 13, 2021

Abstract

Copolymers having General Formula (I):

in which R 1 is chosen from divalent C 4 -C 7 aliphatic groups and divalent C 4 -C 7 heteroaliphatic groups, optionally substituted with one or more C 1 -C 6 aliphatic groups, heteroatoms independently chosen from O, N, and S, or combinations thereof, where: the divalent C 4 -C 7 heteroaliphatic groups include one or two heteroatoms independently chosen from O, N, and S, and the maximum number of heteroatoms in R 1 is two; x is a molar fraction range chosen from 0.05 to 0.95; and y is a molar fraction range chosen from 0.05 to 0.95, where the summation of x and y equals 1. Methods for inhibiting formation of clathrate hydrates in a fluid capable of forming the clathrate hydrates. The methods include contacting the fluid with at least one copolymer of General Formula (I) under conditions suitable for forming the clathrate hydrates.

First claim

What is claimed is:

1. A method for inhibiting formation of clathrate hydrates in a fluid capable of forming the clathrate hydrates, the method comprising:
contacting the fluid with at least one bipolymer of General Formula (I) under conditions suitable for forming the clathrate hydrates:

in which:
R 1 is chosen from divalent C 5 -C 7 aliphatic groups or divalent C 5 -C 7 heteroaliphatic groups, optionally substituted with one or more C 1 -C 6 aliphatic groups, heteroatoms independently chosen from O, N, or S, or combinations thereof, where:
the divalent C 5 -C 7 heteroaliphatic groups comprise one or two heteroatoms independently chosen from O, N, or S, and
the maximum number of heteroatoms in R 1 is two;

x is a molar fraction range chosen from 0.15 to 0.85; and
y is a molar fraction range chosen from 0.15 to 0.85, where the summation of x and y equals 1.

2. The method of claim 1 , where the fluid comprises water host molecules and natural gas guest molecules chosen from methane, ethane, propane, butane, pentane, carbon dioxide, hydrogen sulfide, nitrogen, condensate thereof, or combinations thereof.

3. The method of claim 1 , where:
the clathrate hydrates comprise SI clathrate hydrates, SII clathrate hydrates, SH clathrate hydrates, or combinations thereof, and
the contacting inhibits formation of the SI clathrate hydrates, the SII clathrate hydrates, the SH clathrate hydrates, or the combinations thereof.

4. The method of claim 1 , where the contacting inhibits the formation of the clathrate hydrates at a first subcooling temperature of from 0° C. to 4.0° C.

5. The method of claim 1 , where the contacting inhibits the formation of the clathrate hydrates at a second subcooling temperature of from 4.0° C. to 10.0° C.

6. The method of claim 1 , where the contacting inhibits the formation of the clathrate hydrates in a pressure range of from 40 bars to 200 bars.

7. The method of claim 1 , where the fluid is contacted with a composition comprising the at least one bipolymer of General Formula (I) and one or more corrosion inhibitors, scale inhibitors, thermodynamic hydrate inhibitors, low dose hydrate inhibitors, anti-agglomerates, solvents, or combinations thereof.

8. The method of claim 1 , where:

is chosen from

9. The method of claim 1 , where the fluid is contacted with the at least one bipolymer at a tie-in platform.

10. The method of claim 1 , where the fluid is flowing in a pipeline.

11. The method of claim 1 , where:

is chosen from

12. The method of claim 11 , wherein x is a molar fraction of about 0.5; and y is a molar fraction of about 0.5.

Assignees

• Saudi Arabian Oil Co
• Univ King Fahd Pet & Minerals

Inventors

• Elanany Mohamed
• Majnouni Khalid
• Alessa Rashed
• Al-Malki Abdullah
• Al-Ajwad Hassan
• Al-Daous Mohammed
• Ali Shaikh Asrof

Classifications

• C08K5/34

  Heterocyclic compounds having nitrogen in the ring · CPC title

• C08G73/02

  Polyamines · CPC title

• C08K5/01

  Hydrocarbons {(C08K5/0091 takes precedence)} · CPC title

• C08G73/1092 Primary

  Polysuccinimides · CPC title

• C10L3/107 Primary

  Limiting or prohibiting hydrate formation · CPC title