Method of application of sliding-ring polymers to enhance elastic properties in oil-well cement

US11279864B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11279864-B2
Application numberUS-201916593820-A
CountryUS
Kind codeB2
Filing dateOct 4, 2019
Priority dateOct 4, 2019
Publication dateMar 22, 2022
Grant dateMar 22, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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This document relates to methods for improving the tensile and elastic properties of cement of an oil well using cement compositions that contain sliding-ring polymer additives. The cement compositions containing the sliding-ring polymer additives exhibit increased stiffness while having a minimum impact on compressive strength, as compared to the same cement without the sliding-ring polymer additive.

First claim

Opening claim text (preview).

What is claimed is: 1. A cement composition comprising: cement; and a sliding-ring polymer additive comprising at least two molecules of a polyrotaxane, wherein the polyrotaxane comprises: a linear polymer; at least one ring compound, wherein the linear polymer is threaded through the opening of the ring compound; and stopper groups disposed at both end terminals of the linear polymer; wherein at least one of the linear polymer and the ring compound is substituted with a hydrophobic group or a non-ionic group or combination thereof; and the at least two molecules of polyrotaxane are cross-linked to each other through a chemical bond. 2. The composition of claim 1 , wherein the linear polymer is selected from the group consisting of polyvinyl alcohol, polyvinylpyrrolidone, poly(meth)acrylic acid, a cellulose-based resin, polyacrylamide, polyethylene oxide, polyethylene glycol, polypropylene glycol, a polyvinyl acetal-based resin, polyvinyl methyl ether, polyamine, polyethyleneimine, casein, gelatin, starch, a polyolefin-based resin, a polyester resin, a polyvinyl chloride resin, a polystyrene-based resin, an acrylic resin, a polycarbonate resin, a polyurethane resin, a vinyl chloride-vinyl acetate copolymer resin, a polyvinylbutyral resin, polyisobutylene, polytetrahydrofuran, polyaniline, acrylonitrile-butadiene-styrene copolymer (ABS resin), a polyamide, a polyimide, a polydiene, a polysiloxane, a polysulfone, a polyimine, a polyacetic anhydride, a polyurea, a polysulfide, a polyphosphazene, a polyketone, a polyphenylene, a polyhaloolefin; and derivatives and copolymers thereof. 3. The composition of claim 2 , wherein the linear polymer is selected from the group consisting of polypropylene glycol, polytetrahydrofuran, polydimethylsiloxane, polyethylene and polypropylene copolymer, and polyethylene glycol. 4. The composition of claim 3 , wherein the linear polymer is polyethylene glycol. 5. The composition of claim 1 , wherein the linear polymer has a molecular weight of about 2000 g/mol to about 50,000 g/mol, about 8000 g/mol to about 30,000 g/mol, about 15,000 g/mol to about 25,000 g/mol, or about 10,000 g/mol to about 50,000 g/mol. 6. The composition of claim 1 , wherein the linear polymer has a molecular weight greater than about 10,000 g/mol, greater than about 20,000 g/mol, or greater than about 35,000 g/mol. 7. The composition of claim 1 , wherein the ring compound comprises one or more of an —OH group, an —NH 2 group, a —COOH group, an epoxy group, a vinyl group, a thiol group, a photo-crosslinkable group, and combinations thereof. 8. The composition of claim 7 , wherein the photo-crosslinkable group is selected from the group consisting of cinnamic acid, coumarin, chalcone, anthracene, styrylpyridine, styrylpyridinium salt, and styrylquinolium salt. 9. The composition of claim 7 , wherein the ring compound is a cyclodextrin or cyclodextrin derivative. 10. The composition of claim 9 , wherein the cyclodextrin is selected from the group consisting of α-cyclodextrin (α-CD), β-cyclodextrin (β-CD), and γ-cyclodextrin (γ-CD) and combinations thereof. 11. The composition of claim 9 , wherein the ring compound is a cyclodextrin and a part or all of the hydroxyl groups (—OH) of the cyclodextrin is substituted with a hydrophobic group or non-ionic group or combination thereof. 12. The composition of claim 11 , wherein substitution of the hydroxyl group with the hydrophobic group or non-ionic group or combination thereof is about 10% to about 100% of the total hydroxyl groups of the total cyclodextrin molecules. 13. The composition of claim 9 , wherein at least one hydroxyl group of at least one cyclodextrin molecule in each of the at least two molecules of polyrotaxane is involved in cross-linking. 14. The composition of claim 1 , wherein ring compound has an inclusion amount ranging from 0.001 to 0.61 relative to 1 which is the maximum inclusion amount of the ring compound capable of being included by the linear polymer. 15. The composition of claim 1 , wherein the stopper group is selected from the group consisting of a dinitrophenyl, a cyclodextrin, adamantane, trityl, a fluorescein, a pyrene, a substituted benzene, a polycyclic aromatic, and steroids. 16. The composition of claim 15 , wherein the stopper group is adamantane or trityl. 17. The composition of claim 1 , wherein the hydrophobic group is selected from the group consisting of alkyl group, benzyl group, benzene derivative-containing group, acyl group, silyl group, trityl group, tosyl group, a polymer, and groups bonded through a urethane bond, ester bond or ether bond. 18. The composition of claim 17 , wherein the polymer is a polycaprolactone. 19. The composition of claim 1 , wherein the non-ionic group is selected from the group consisting of: an —OR group, wherein R is a linear or branched alkyl group having 1-12 carbons, a linear or branched alkyl group having 2-12 carbons and at least one ether group, a cycloalkyl group having 3-12 carbons, a cycloalkyl ether group having 2-12 carbons or a cycloalkyl thioether group having 2-12 carbons; an —O—R′—X group, wherein R′ is a group resulting from removal of one hydrogen in a linear or branched alkyl group having 1-12 carbons, a group resulting from removal of one hydrogen in a linear or branched alkyl group having 2-12 carbons and at least one ether group, a group resulting from removal of one hydrogen in a cycloalkyl group having 3-12 carbons, a group resulting from removal of one hydrogen in a cycloalkyl ether group having 2-12 carbons or a group resulting from removal of one hydrogen in a cycloalkyl thioether group having 2-12 carbons, and X is —OH, —NH 2 or —SH; an —O—CO—NH—R 1 group, wherein R 1 is a linear or branched alkyl group having 1-12 carbons, a linear or branched alkyl group having 2-12 carbons and at least one ether group, a cycloalkyl group having 3-12 carbons, a cycloalkyl ether group having 2-12 carbons or a cycloalkyl thioether group having 2-12 carbons; an —O—CO—R 2 group, wherein R 2 is a linear or branched alky 1 group having 1-12 carbons, a linear or branched alkyl group having 2-12 carbons and at least one ether group, a cycloalkyl group having 3-12 carbons, a cycloalkyl ether group having 2-12 carbons or a cycloalkyl thioether group having 2-12 carbons; an —O—Si—R 3 group, wherein R 3 is a linear or branched alkyl group having 1-12 carbons, a linear or branched alkyl group having 2-12 carbons and at least one ether group, a cycloalkyl group having 3-12 carbons, a cycloalkyl ether group having 2-12 carbons or a cycloalkyl thioether group having 2-12 carbons; and an —O—CO—O—R 4 group, wherein R 4 is a linear or branched alkyl group having 1-12 carbons, a linear or branched alkyl group having 2-12 carbons and at least one ether group, a cycloalkyl group having 3-12 carbons, a cycloalkyl ether group having 2-12 carbons or a cycloalkyl thioether group having 2-12 carbons. 20. The composition of claim 1 , wherein the at least two molecules of polyrotaxane are chemically bonded by a cross-linking agent. 21. The composition of claim 20 , wherein the cross-linking agent is selected from the group consisting of cyanuric chloride, trimesoyl chloride, terephthaloyl chloride, epichlorohydrin, dibromobenzene, glutaraldehyde, phenylene diisocyanates, tolylene diisocyanates, divinylsulfone, 1,1′-carbonyldiimidazole, and alkoxysilanes. 22. The composition of claim 1 , wherein the sliding-ring polymer additive comprises a polyrotaxane wherein t

Assignees

Inventors

Classifications

  • Cellulose or derivatives thereof · CPC title

  • containing phosphorus in the anion, e.g. phosphates · CPC title

  • Cross-linked polymers · CPC title

  • containing hydraulic cements other than calcium sulfates · CPC title

  • C09K8/467Primary

    containing additives for specific purposes · CPC title

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What does patent US11279864B2 cover?
This document relates to methods for improving the tensile and elastic properties of cement of an oil well using cement compositions that contain sliding-ring polymer additives. The cement compositions containing the sliding-ring polymer additives exhibit increased stiffness while having a minimum impact on compressive strength, as compared to the same cement without the sliding-ring polymer ad…
Who is the assignee on this patent?
Saudi Arabian Oil Co
What technology area does this patent fall under?
Primary CPC classification C09K8/467. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Mar 22 2022 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 4 related publications on this page (citations in our corpus or others sharing the same primary CPC).