Methods and Compositions to use Shape Changing Polymers in Subterranean Formations
US-2016312098-A1 · Oct 27, 2016 · US
US11359128B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11359128-B2 |
| Application number | US-201415113219-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 21, 2014 |
| Priority date | Feb 21, 2014 |
| Publication date | Jun 14, 2022 |
| Grant date | Jun 14, 2022 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
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.
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.
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
Related publications grouped by family.
Answers are generated from the same data shown on this page.