Kinetic hydrate inhibitors with pendent amino functionality

US9840654B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9840654-B2
Application numberUS-201213679457-A
CountryUS
Kind codeB2
Filing dateNov 16, 2012
Priority dateNov 16, 2012
Publication dateDec 12, 2017
Grant dateDec 12, 2017

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

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A kinetic gas hydrate inhibitor is provided as a polyester polymer with a plurality of amino or ammonium groups pendent directly from the backbone. A composition containing concentrated kinetic inhibitor is injected into gas wells, or into other systems involving transporting liquid gas mixtures through a conduit. Use of the kinetic inhibitor prevents formation of gas hydrates under conditions of temperature and pressure where they would otherwise occur.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for inhibiting gas hydrate formation in an aqueous phase that is in contact with a gaseous or liquid organic phase, the method comprising: preparing a composition comprising 10-50% by weight of a kinetic inhibitor, and injecting the composition into the aqueous phase to provide the aqueous phase with 0.01-3% by weight of the kinetic inhibitor, wherein the kinetic inhibitor is a polyester polymer comprising a polyester backbone chain and a plurality of pendent amino groups that are directly attached to the polyester backbone chain, and wherein the polyester polymer is produced by polymerizing a plurality of acid monomers with a plurality of polyols, each of the acid monomers comprising the pendent amino group. 2. The method according to claim 1 , wherein the aqueous phase comprises 0.01-2 weight % of the kinetic inhibitor. 3. The method according to claim 1 , wherein the inhibitor is made by polymerizing an amino functional diacid, diester, or mixed acid ester with an alkylene or oxyalkylene diol or triol. 4. The method according to claim 1 , wherein the inhibitor is made by polymerizing a diacid, diester, or mixed acid ester with an amine functional diol or triol. 5. The method according to claim 1 , wherein the acid monomers have the following structure and the polyols have the following structure B(OH) n wherein X is amino, A is alkylene of 1 to 40 carbon atoms, R 1 and R 2 are independently —H or alkyl, B is selected from branched or unbranched alkylene and branched or unbranched oxa-substituted alkylene, and n is 2, 3, or 4. 6. The method according to claim 5 wherein A is C 2 -C 6 alkylene, B is C 2 -C 12 alkylene or polyoxyalkylene, and n is 2 or 3. 7. The method according to claim 5 , wherein A is C 3 alkylene or C 4 alkylene and the polyol component is ethylene glycol, diethylene glycol, or triethylene glycol. 8. The method according to claim 5 , wherein the acid monomers are selected from the group consisting of aspartic acid, glutamic acid, protected aspartic acid, and protected glutamic acid. 9. The method according to claim 8 , wherein the polyols are selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, and tetraethylene glycol. 10. The method according to claim 1 , further comprising providing the aqueous phase with a synergist made of C 3 to C 10 ethers of C 2 to C 4 glycols. 11. The method according to claim 10 , wherein the synergist is C 3 to C 6 ethers of C 2 to C 3 glycols. 12. The method according to claim 10 , wherein the synergist is selected from the group consisting of 2-butoxyethanol, 2-isopropoxyethanol, 1-propoxy-2-propanol, 2-(2-butoxyethoxy)ethanol, 1-butoxy-2-propanol, and 2-propoxyethanol. 13. The method according to claim 1 , wherein a solution of the kinetic inhibitor is greater than 20% biodegradable, exhibits no inherent cloud point behavior upon heating, and gives an induction time greater than 24hours at 6° C. subcooling using synthetic natural gas.

Assignees

Inventors

Classifications

  • Hydrates inhibition by using well treatment fluids containing inhibitors of hydrate formers · CPC title

  • C09K8/528Primary

    inorganic depositions, e.g. sulfates or carbonates · CPC title

  • C09K8/52Primary

    Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning · CPC title

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What does patent US9840654B2 cover?
A kinetic gas hydrate inhibitor is provided as a polyester polymer with a plurality of amino or ammonium groups pendent directly from the backbone. A composition containing concentrated kinetic inhibitor is injected into gas wells, or into other systems involving transporting liquid gas mixtures through a conduit. Use of the kinetic inhibitor prevents formation of gas hydrates under conditions …
Who is the assignee on this patent?
M-I L L C, Schlumberger Norge As
What technology area does this patent fall under?
Primary CPC classification C09K8/528. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 12 2017 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).