Acrylamide-based copolymers, terpolymers, and use as hydrate inhibitors

US10189986B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10189986-B2
Application numberUS-201715584382-A
CountryUS
Kind codeB2
Filing dateMay 2, 2017
Priority dateMay 6, 2016
Publication dateJan 29, 2019
Grant dateJan 29, 2019

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  1. Title

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Copolymers having General Formula (I): in which R 1 , R 2 , and R 3 are chosen from C 1 to C 30 aliphatic groups, R 4 is chosen from divalent C 4 to C 7 linear aliphatic groups and divalent C 4 to C 7 linear heteroaliphatic groups, optionally substituted with one or more C 1 -C 6 linear aliphatic groups, C 1 -C 6 branched aliphatic groups, or combination thereof, R 5 , R 6 , and R 7 are each independently chosen from methyl or hydrogen, x is chosen from 0 to 0.8, y is chosen from 0 to 0.8, when y is 0, x is greater than 0, and when x is 0, y is greater than 0, and z is chosen from 0.1 to 0.9. The summation of x, y, and z equals 1. Methods for inhibiting formation of clathrate hydrates in a fluid capable of forming the clathrate hydrates, including contacting the fluid with at least one copolymer of General Formula (I).

First claim

Opening claim text (preview).

What is claimed is: 1. A terpolymer having General Formula (I): in which: R 1 , R 2 , and R 3 are each independently chosen from C 1 to C 8 saturated aliphatic groups, R 4 is chosen from divalent C 4 to C 7 linear aliphatic groups or divalent C 4 to C 7 linear heteroaliphatic groups, optionally substituted with one or more C 1 -C 6 linear aliphatic groups, C 1 -C 6 branched aliphatic groups, or combination thereof, where the divalent C 4 to C 7 linear heteroaliphatic groups comprise 1 or 2 heteroatoms independently chosen from O, N, or S, R 5 , R 6 , and R 7 are each independently chosen from methyl or hydrogen, x is a molar fraction range chosen from greater than 0 to 0.8, y is a molar fraction range chosen from greater than 0 to 0.8, z is a molar fraction range chosen from 0.1 to 0.9, where the summation of x, y, and z equals 1, and the terpolymer is random. 2. The terpolymer of claim 1 , where: R 4 is chosen from divalent C 4 to C 7 linear aliphatic groups, x is a molar fraction range chosen from greater than 0 to 0.5, y is a molar fraction range chosen from greater than 0 to 0.5, and z is a molar fraction range chosen from 0.2 to 0.75. 3. The terpolymer of claim 1 , where: R 1 , R 2 , and R 3 are each independently chosen from methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, sec-pentyl, isopentyl, tert-pentyl, n-hexyl, or sec-hexyl, R 4 is chosen from divalent C 4 to C 6 linear aliphatic groups, x is a molar fraction range chosen from greater than 0 to 0.2, y is a molar fraction range chosen from greater than 0 to 0.5, and z is a molar fraction range chosen from 0.2 to 0.75. 4. The terpolymer of claim 1 , where is chosen from 5. The terpolymer of claim 1 , where: R 1 is methyl, R 2 is methyl, R 3 is isopropyl, x is a molar fraction range chosen from 0.5 to 0.75, y is a molar fraction range chosen from 0.1 to 0.25, and z is a molar fraction range chosen from 0.1 to 0.25. 6. The terpolymer of claim 1 , where: x is a molar fraction range chosen from 0.5 to 0.75, and z is a molar fraction range chosen from 0.25 to 0.5. 7. The terpolymer of claim 1 , where the viscosity average molecular weight of the terpolymer is in the range of from 1,000 g/mol to 1,000,000 g/mol. 8. 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 terpolymer of General Formula (I) under conditions suitable for forming the clathrate hydrates: in which: R 1 , R 2 , and R 3 are each independently chosen from C 1 to C 8 saturated aliphatic groups, R 4 is chosen from divalent C 4 to C 7 linear aliphatic groups or divalent C 4 to C 7 linear heteroaliphatic groups, optionally substituted with one or more C 1 -C 6 linear aliphatic groups, C 1 -C 6 branched aliphatic groups, or combination thereof, where the divalent C 4 to C 7 linear heteroaliphatic groups comprise 1 or 2 heteroatoms independently chosen from O, N, or S, R 5 , R 6 , and R 7 are each independently chosen from methyl or hydrogen, x is a molar fraction range chosen from greater than 0 to 0.8, y is a molar fraction range chosen from greater than 0 to 0.8, z is a molar fraction range chosen from 0.1 to 0.9, where the summation of x, y, and z equals 1, and the at least one terpolymer is random. 9. The method of claim 8 , where the fluid comprises water host molecules and natural gas guest molecules chosen from methane, ethane, propane, butane, pentane, carbon dioxide, hydrogen sulfide, nitrogen, or combination thereof. 10. The method of claim 8 , where the fluid comprises acid gas guest molecules. 11. The method of claim 8 , where: the clathrate hydrates comprise SI clathrate hydrates, SII clathrate hydrates, or combination thereof and the contacting inhibits formation of the SI clathrate hydrates, the SII clathrate hydrates, or the combination thereof. 12. The method of claim 8 , where the contacting inhibits the formation of the clathrate hydrates at a first subcooling temperature of from 0° C. to 4.0° C. 13. The method of claim 8 , where the contacting inhibits the formation of the clathrate hydrates in a pressure range of from 40 bars to 200 bars. 14. The method of claim 8 , where the fluid is contacted with a composition comprising the at least one terpolymer of Formula (I) and at least one of a corrosion inhibitor or solvent. 15. The method of claim 8 , where: R 4 is chosen from divalent C 4 to C 7 linear aliphatic groups, x is a molar fraction range chosen from greater than 0 to 0.5, y is a molar fraction range chosen from greater than 0 to 0.5, and z is a molar fraction range chosen from 0.2 to 0.75. 16. The method of claim 8 , where: R 4 is chosen from divalent C 4 to C 7 linear aliphatic groups. 17. The method of claim 8 , where: is chosen from x is a molar fraction range chosen from 0.5 to 0.75, y is a molar fraction range chosen from 0.1 to 0.25, and z is a molar fraction range chosen from 0.1 to 0.25. 18. The method of claim 8 , where the viscosity average molecular weight of the at least one terpolymer is in the range of from 1,500 g/mol to 20,000 g/mol. 19. The method of claim 8 , where the fluid is contacted with the at least one terpolymer at a tie-in platform.

Assignees

Inventors

Classifications

  • C08L33/26Primary

    Homopolymers or copolymers of acrylamide or methacrylamide · CPC title

  • by a heterocyclic ring containing nitrogen · CPC title

  • of esters containing halogen, nitrogen, sulfur, or oxygen atoms in addition to the carboxy oxygen · CPC title

  • Polymer mixtures characterised by other features · CPC title

  • Anticorrosion additives · CPC title

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What does patent US10189986B2 cover?
Copolymers having General Formula (I): in which R 1 , R 2 , and R 3 are chosen from C 1 to C 30 aliphatic groups, R 4 is chosen from divalent C 4 to C 7 linear aliphatic groups and divalent C 4 to C 7 linear heteroaliphatic groups, optionally substituted with one or more C 1 -C 6 linear aliphatic groups, C 1 -C 6 branched aliphatic groups, or combination the…
Who is the assignee on this patent?
Saudi Arabian Oil Co, Univ King Fahd Pet & Minerals
What technology area does this patent fall under?
Primary CPC classification C08L33/26. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).