Cementing compositions and methods

US11359128B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11359128-B2
Application numberUS-201415113219-A
CountryUS
Kind codeB2
Filing dateFeb 21, 2014
Priority dateFeb 21, 2014
Publication dateJun 14, 2022
Grant dateJun 14, 2022

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Cementing compositions including a di- or poly epoxide resin, and amine hardener, and a di- or polyfunctional alkylphosphonate ester fortifier and methods of using the cementing compositions such as in a subterranean zone penetrated by a well bore.

First claim

Opening claim text (preview).

The invention claimed is: 1. An epoxide resin cementing composition for use in a subterranean well, the composition comprising: (a) a di- or poly epoxide resin; (b) polyoxypropylenediamine, wherein the polyoxypropylenediamine is present from 5 wt % to 15 wt % based on the total weight of the composition; and (c) a di- or polyfunctional alkylphosphonate ester fortifier, wherein the fortifier is present from 3 wt % to 15 wt % based on the total weight of the composition; wherein the di- or polyfunctional alkylphosphonate ester is one or more compounds selected from the group consisting of: hexa(methyl or ethyl) 1,2,3-propanetriyltrisphosphonate; tetra(methyl or ethyl) 1,x-phenylenebis(methylene)diphosphonate, wherein x=2-4; tetra(methyl or ethyl) 1,x-naphthalenediylbis(methylene)diphosphonate, wherein x=2-8; tetra(methyl or ethyl) 2,x-pyridinediylbis(methylene)diphosphonate, wherein x=3-6; tetra(methyl or ethyl) 2,5-furandiylbis(methylene)diphosphonate; tetra(methyl or ethyl) 3-alkyl-2,5-furandiylbis (methylene) diphosphonate; and tetra(methyl or ethyl) 3-alkyl-2,5-thiophenediylbis (methylene) diphosphonate (d) a density modifier; wherein the glass transition temperature of the composition is increased by the presence of the fortifier from 15° F. to 50° F. compared to the identical composition without the fortifier, and wherein the composition has a viscosity of at least 5 Bc to 90 Bc prior to curing, and wherein the composition does not comprise any Portland cement. 2. The composition according to claim 1 , wherein (a) the di- or poly epoxide resin is one or more compounds selected from the group consisting of an epichlorohydrin adduct of a bisphenol, an epichlorohydrin adduct of a novolac, an epichlorohydrin adduct of an alkyl diol, and an epichlorohydrin adduct of a cycloalkyl diol. 3. The composition according to claim 2 , wherein (a) the di- or poly epoxide resin is one or more compounds selected from the group consisting of a bisphenol A epoxy resin, a bisphenol F epoxy resin, an epoxy novolac resin, a diglycidyl ether of an aliphatic diol, a diglycidyl ether of a polyethylene glycol, a diglycidyl ether of a polypropylene glycol, a cyclohexanedimethanol diglycidyl ether, a butanediol diglycidyl ether, trimethylolpropane triglycidyl ether, a hexanediol diglycidyl ether, N,N-diglycidyl-4-glycidyloxyaniline, 4,4′-methylenebis(N,N-diglycidylaniline), neopentyl glycol diglycidyl ether, resorcinol diglycidyl ether, tetraphenylolethane glycidyl ether, tris(2,3-epoxypropyl) isocyanurate, and tris(4-hydroxyphenyl)methane triglycidyl ether. 4. The composition according to claim 3 , wherein (a) the di- or poly epoxide resin is a bisphenol A diglycidyl ether resin and/or a cyclohexanedimethanol diglycidyl ether. 5. The composition according to claim 1 , wherein the di- or polyfunctional alkylphosphonate ester fortifier is an ethyl or methyl ester. 6. The composition according to claim 1 , wherein the di- or polyfunctional alkyl phosphonate ester is one or more compounds selected from the group consisting of: wherein R is methyl or ethyl; and R′ is a C 1 -C 15 aliphatic or branched alkyl, which may be optionally substituted. 7. The composition according to claim 1 , where (a) the di- or poly epoxide resin is in an amount of from 20 wt. % to 90 wt. %, based on the total weight of the composition. 8. The composition according to claim 1 , wherein (b) the amine hardener is in an amount of from 5 wt. % to 75 wt. %, based on the total weight of the epoxy resin. 9. The composition according to claim 1 , wherein the density modifier is barite. 10. The composition according to claim 1 , further comprising: (e) a silane coupling agent, and (f) a diluent. 11. An epoxide resin cement composition for use in a subterranean well, the composition comprising: (a) 30 wt. % to 90 wt. %, based on the total weight of the composition, of a bisphenol A diglycidyl ether resin and/or a cyclohexanedimethanol diglycidyl ether; (b) 5 wt. % to 15 wt. %, based on the total weight of component (a), of polyoxypropylenediamine; (c) 3 wt % to 15 wt % based on the total weight of the composition, of one or more di- or polyfunctional alkylphosphonate esters selected from the group consisting of: hexa(methyl or ethyl) 1,2,3-propanetriyltrisphosphonate; tetra(methyl or ethyl) 1,x-phenylenebis(methylene)diphosphonate, wherein x=2-4; tetra(methyl or ethyl) 1,x-naphthalenediylbis(methylene)diphosphonate, wherein x=2-8; tetra(methyl or ethyl) 2,x-pyridinediylbis(methylene)diphosphonate, wherein x=3-6; tetra(methyl or ethyl) 2,5-furandiylbis(methylene)diphosphonate; tetra(methyl or ethyl) 3-alkyl-2,5-furandiylbis(methylene)diphosphonate; and tetra(methyl or ethyl) 3-alkyl-2,5-thiophenediylbis(methylene)diphosphonate; (d) a density modifier; (e) optionally a silane coupling agent; and (f) optionally a diluent, wherein the glass transition temperature of the composition is increased by the presence of the fortifier from 15° F. to 50° F. compared to the identical composition without the fortifier, and wherein the composition has a viscosity of at least 5 Bc to 90 Bc prior to curing, and wherein the composition does not comprise any Portland cement. 12. A system for cementing in a subterranean zone penetrated by a well bore comprising: mixing equipment in which cement comprising a composition according to claim 1 is mixed; and pumping equipment by which the mixed cement is placed in the subterranean zone. 13. A method of cementing in a subterranean zone penetrated by a well bore comprising: (a) providing a composition according to claim 1 ; (b) placing the composition in the subterranean zone using pumping equipment; and (c) allowing the composition to fully cure. 14. A method of increasing the T g of a cured cement, plug, or seal used in a subterranean zone penetrated by a well bore comprising: (a) dissolving a di- or polyfunctional alkylphosphonate ester fortifier in a di- or poly epoxide resin; (b) adding polyoxypropylenediamine to the di- or poly epoxide resin having the di- or polyfunctional alkylphosphonate ester fortifier dissolved therein to form an uncured composition, wherein the polyoxypropylenediamine is present from 5 wt % to 15 wt % based on the total weight of the composition; (c) pumping the uncured composition into a subterranean zone penetrated by a well bore; and (d) allowing the uncured composition to cure and form a cured cement, plug, or seal having a T g higher than an otherwise identical cured cement, plug, or seal formed without addition of the di- or polyfunctional alkylphosphonate ester fortifier.

Assignees

Inventors

Classifications

  • Apparatus or methods for multilateral well technology, e.g. for the completion of or workover on wells with one or more lateral branches · CPC title

  • containing heterocyclic rings not representing cyclic esters of phosphonic acids · CPC title

  • Methods or devices for cementing, for plugging holes, crevices or the like · CPC title

  • Organo-silicon compounds · CPC title

  • Esters, e.g. lactones · CPC title

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What does patent US11359128B2 cover?
Cementing compositions including a di- or poly epoxide resin, and amine hardener, and a di- or polyfunctional alkylphosphonate ester fortifier and methods of using the cementing compositions such as in a subterranean zone penetrated by a well bore.
Who is the assignee on this patent?
Halliburton Energy Services Inc
What technology area does this patent fall under?
Primary CPC classification C09K8/44. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 14 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).