Wellbore servicing methods and compositions comprising degradable polymers

US2016304773A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016304773-A1
Application numberUS-201615195724-A
CountryUS
Kind codeA1
Filing dateJun 28, 2016
Priority dateOct 25, 2012
Publication dateOct 20, 2016
Grant date

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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

Official abstract text for this publication.

A method of servicing a wellbore comprising providing a degradable polymer and a delayed action construct within a portion of a wellbore, a subterranean formation or both; wherein the delayed action construct comprises (i) a degradation accelerator comprising an alkanolamine, an oligomer of aziridine, a polymer of azridine, a diamine, or combinations thereof, (ii) a solid support, and (iii) an encapsulating material; and placing the wellbore servicing fluid comprising the degradable polymer and delayed action construct into the wellbore, the subterranean formation or both.

First claim

Opening claim text (preview).

What is claimed is: 1 . A method of servicing a wellbore comprising: providing a first component comprising a degradable polymer and a second component comprising a delayed action construct within a portion of a wellbore, a subterranean formation or both; wherein the delayed action construct comprises (i) a degradation accelerator comprising an alkanolamine, a polymer of aziridine, a diamine, or combinations thereof, (ii) a solid support, and (iii) an encapsulating material; and placing the wellbore servicing fluid comprising the degradable polymer and delayed action construct into the wellbore, the subterranean formation or both. 2 . The method of claim 1 wherein the alkanolamine-is selected from the group consisting of: ethanolamine, triethanolamine, monoethanolamine, diethanolamine, diglycolamine, di-2-propanolamine, N-ethyldiethanolamine, 2-amino-2-methyl-1-propanol, 2-piperidineethanol, aminopropane diol, and any combination thereof. 3 . The method of claim 1 wherein the alkanolamine comprises a compound characterized by Formula I: where R 1 and R 2 may each independently be hydrogen, an unsubstituted alkyl chain comprising from about 1 to about 6 carbon atoms, or a substituted alkyl chain comprising from about 3 to about 6 carbon atoms and X comprises a substituted or unsubstituted alkylene having from about 1 to about 4 carbon atoms. 4 . The method of claim 1 wherein the diamine comprises a compound characterized by general Formula V: where R 5 , R 6 , R 7 , and R 8 may each independently be hydrogen, an unsubstituted alkyl chain having from about 1 to about 3 carbon atoms, or a substituted alkyl chain having from about 2 to about 4 carbon atoms and Z comprises a substituted or unsubstituted alkylene chain having from about 2 to about 6 carbon atoms. 5 . The method of claim 1 wherein the degradation accelerator is present in the well bore servicing fluid in an amount of from about 0.1 wt. % to about 50 wt. % based on the total weight of the wellbore servicing fluid. 6 . The method of claim 1 wherein the degradable polymer comprises a polymer selected from the group consisting of: an aliphatic polyester, a poly(lactide), a poly(glycolide), a poly(ε-caprolactone), a poly(hydroxy ester ether), a poly(hydroxybutyrate), a poly(anhydride), a polycarbonate, a polyether ester, a polyester amide, a copolymer thereof, and any combination thereof. 7 . The method of claim 6 wherein the degradable polymer comprises a poly(lactide). 8 . The method of claim 1 wherein the degradable polymer comprises a copolymer of lactic and glycolic acid. 9 . The method of claim 1 wherein the degradable polymer further comprises a plasticizer. 10 . The method of claim 9 wherein the plasticizer is selected from the group consisting of: a polyethylene glycol (PEG); a polyethylene oxide; an oligomeric lactic acid; a citrate ester; a glucose monoester; a partially hydrolyzed fatty acid ester; a PEG monolaurate; a triacetin; a poly(ε-caprolactone); a poly(hydroxybutyrate); a glycerin-1-benzoate-2,3-dilaurate; a glycerin-2-benzoate-1,3-dilaurate; a bis(butyl diethylene glycol)adipate; an ethylphthalylethyl glycolate; a glycerin diacetate monocaprylate; a diacetyl monoacyl glycerol; a polypropylene glycol; an epoxy derivative of a polypropylene glycol; a poly(propylene glycol)dibenzoate; a dipropylene glycol dibenzoate; a glycerol; an ethyl phthalyl ethyl glycolate; a poly(ethylene adipate)distearate; a di-iso-butyl adipate, and any combination thereof. 11 . The method of claim 1 wherein the solid support is selected from the group consisting of: a clay, zeolite, polymeric resin, lignite, inorganic oxide, and any combination thereof. 12 . The method of claim 1 wherein the solid support comprises a particulate porous material. 13 . The method of claim 12 wherein the particulate porous material is selected from the group consisting of: diatomaceous earth, silica, alumina, a metal salt of an alumino-silicate, a clay, hydrotalcite, a styrenedivinylbenzene-based material, a cross-linked polyalkylacrylate ester, a cross-linked modified starch, and any combination thereof. 14 . The method of claim 1 wherein the encapsulating material is selected from the group consisting of: a cellulose-based polymer, a cellulose ether, a methylcellulose, a hydroxypropyl methylcellulose, an ethylhydroxyethylcellulose, a methylhydroxyethylcellulose, a bacterial based gum, a plant based gum, a xanthan, a diutan, a gellan, a gum tragacanth, a pestan, and any combination thereof. 15 . The method of claim 1 wherein the encapsulating material is selected from the group consisting of: an EDPM rubber, a polyvinyldichloride, a nylon, a wax, a polyurethane, a cross-linked partially hydrolyzed acrylic, a crosslinked polyurethane, and any combination thereof. 16 . The method of claim 1 wherein the encapsulating material is selected from the group consisting of: tung oil, linseed oil, and any combination thereof. 17 . The method of claim 1 wherein the degradation accelerator is spray coated onto the solid support. 18 . The method of claim of claim 1 wherein the degradation accelerator comprises an alkanolamine and wherein the encapsulating material comprises a crosslinked polyurethane. 19 . The method of claim 1 wherein the degradation accelerator comprises a polymer of aziridine and wherein the encapsulating material comprises a crosslinked polyurethane. 20 . The method of claim 1 wherein the degradation accelerator comprises a diamine and wherein the encapsulating material comprises a crosslinked polyurethane.

Assignees

Inventors

Classifications

  • by forming crevices or fractures · CPC title

  • C09K8/885Primary

    obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title

  • combined with additives added for specific purposes · CPC title

  • C09K8/035Primary

    Organic additives · CPC title

  • Spacer compositions, e.g. compositions used to separate well-drilling from cementing masses · CPC title

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What does patent US2016304773A1 cover?
A method of servicing a wellbore comprising providing a degradable polymer and a delayed action construct within a portion of a wellbore, a subterranean formation or both; wherein the delayed action construct comprises (i) a degradation accelerator comprising an alkanolamine, an oligomer of aziridine, a polymer of azridine, a diamine, or combinations thereof, (ii) a solid support, and (iii) an …
Who is the assignee on this patent?
Halliburton Energy Services Inc
What technology area does this patent fall under?
Primary CPC classification C09K8/885. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Oct 20 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).