Scale-inhibiting cocrystals for treatment of a subterranean formation

Patent metadata

Field	Value
Publication number	US-10253244-B2
Application number	US-201314897431-A
Country	US
Kind code	B2
Filing date	Sep 4, 2013
Priority date	Sep 4, 2013
Publication date	Apr 9, 2019
Grant date	Apr 9, 2019

Abstract

The present invention relates to cocrystals including a scale-inhibiting compound, and methods of using the cocrystals for treating a subterranean formation. In various embodiments, the present invention provides a method of treating a subterranean formation including obtaining or providing a composition including cocrystals. Each cocrystal independently includes a scale-inhibiting compound and a secondary material. The method also includes placing the composition in a subterranean formation.

First claim

What is claimed is:

1. A method of treating a subterranean formation, the method comprising:
placing in a subterranean formation a composition comprising cocrystals, each cocrystal independently comprising:
a scale-inhibiting compound; and
a secondary material,
wherein
(A) the cocrystal is formed in a forming method selected from the group consisting of
(i) a melting method comprising the steps of
(a) melting and blending together the scale-inhibiting compound and the secondary material to form a blend and
(b) allowing the blend to cool and recrystallize to form the cocrystal, and

(ii) a dissolving method comprising the steps of
(a) dissolving the scale-inhibiting compound and the secondary material in a solution and
(b) (1) allowing the solution to evaporate to form the cocrystal, or (2) reducing the solubility of the scale-inhibiting compound and the secondary material in the solution to form the cocrystal and

(B) the scale-inhibiting compound and the secondary material are present in the cocrystal at a mole ratio of about 1:0.01 to about 1:100; and

exposing at least some of the cocrystals to a compression wave to dissociate the scale-inhibiting compound from the cocrystal to provide a released scale-inhibiting compound.

2. The method of claim 1 , wherein the method comprises hydraulic fracturing or a squeeze operation.

3. The method of claim 2 , further comprising treating the subterranean formation with the released scale-inhibiting compound to provide scale inhibition, wherein the scale inhibition comprises a reaction between scale-forming materials and the released scale-inhibiting compound.

4. The method of claim 1 , wherein the composition further comprises a viscosifier comprising a gel or crosslinked gel.

5. The method of claim 1 , wherein the cocrystal comprises a crystalline structure comprising a unit cell comprising both the scale-inhibiting compound and the at least one secondary material.

6. The method of claim 5 , wherein the crystalline structure is different from a crystal structure of a crystal of the scale-inhibiting compound alone and different from a crystal structure of a crystal of the secondary material alone.

7. The method of claim 1 , wherein the cocrystals are at least partially coated on a proppant.

8. The method of claim 1 , wherein the cocrystals are at least partially encapsulated by a protective shell.

9. The method of claim 1 , wherein the scale-inhibiting compound is at least one of a phosphonate, phosphate, sulfonate, acrylate, and a carboxylate.

10. The method of claim 1 , wherein the scale-inhibiting compound comprises at least one of a —P(O)(OZ)OZ, —S(O)(O)OZ, and a —C(O)OZ group, wherein each Z is independently selected from the group consisting of —H and Cl + , and wherein Cl + is a counterion.

11. The method of claim 1 , wherein the scale-inhibiting compound is a polymer formed from a compound having one of the following structures:

wherein:
R 1 is selected from the group consisting of —P(O)(OZ)OZ,
—S(O)(O)OZ, —C(O)OZ, C 1 -C 20 hydrocarbyl, C 4 -C 20 aryl, and C 1 -C 20 heteroaryl, wherein the hydrocarbyl, aryl, and heteroaryl group is substituted or unsubstituted, wherein the hydrocarbyl group is optionally interrupted by 1, 2, or 3 heteroatoms independently selected from 0, S, and substituted or unsubstituted N, wherein the hydrocarbyl, aryl, and heteroaryl group is substituted by at least one group selected from the group consisting of —P(O)(OZ)OZ, —S(O)(O)OZ, and —C(O)OZ, wherein each Z is independently selected from the group consisting of H and Cl + , and wherein Cl + is a counterion; and

R 2 , R 3 , R 4 are independently selected from the group consisting of —H, C 1 -C 20 hydrocarbyl, C 4 -C 20 aryl, and C 1 -C 20 heteroaryl, wherein the hydrocarbyl, aryl, and heteroaryl group is substituted or unsubstituted, and wherein the hydrocarbyl group is optionally interrupted by 1, 2, or 3 heteroatoms independently selected from O, S, and substituted or unsubstituted N.

12. The method of claim 1 , wherein the scale-inhibiting compound comprises at least one of the following structures as a repeating unit:

wherein:
R 1 is selected from the group consisting of —P(O)(OZ)OZ,
—S(O)(O)OZ, —C(O)OZ, C 1 -C 20 hydrocarbyl, C 4 -C 20 aryl, and C 1 -C 20 heteroaryl, wherein the hydrocarbyl, aryl, and heteroaryl group is substituted or unsubstituted, wherein the hydrocarbyl group is optionally interrupted by 1, 2, or 3 heteroatoms independently selected from O, S, and substituted or unsubstituted N, wherein the hydrocarbyl, aryl, and heteroaryl group is substituted by at least one group selected from the group consisting of —P(O)(OZ)OZ, —S(O)(O)OZ, and —C(O)OZ, wherein each Z is independently selected from the group consisting of —H and Cl + , and wherein Cl + is a counterion; and

R 2 , R 3 , R 4 are independently selected from the group consisting of —H, C 1 -C 20 hydrocarbyl, C 4 -C 20 aryl, and C 1 -C 20 heteroaryl, wherein the hydrocarbyl, aryl, and heteroaryl group is substituted or unsubstituted, and wherein the hydrocarbyl group is optionally interrupted by 1, 2, or 3 heteroatoms independently selected from O, S, and substituted or unsubstituted N.

13. The method of claim 1 , wherein the scale-inhibiting compound is a polymer formed from at least one of acrylic acid, aspartic acid, fumaric acid, methacrylic acid, hydroxypropyl acrylic acid, vinyl phosphonic acid, vinylidene diphosphonic acid, maleic anhydride, itaconic acid, crotonic acid, maleic acid, mesoconic acid, citraconic acid, styrene sulfonic acid, allyl sulfonic acid, methallyl sulfonic acid, vinyl sulfonic acid, and a salt thereof.

14. The method of claim 1 , wherein the scale-inhibiting compound is at least one of hexamethylenediamine tetrakis(methylene phosphonic acid), poly(aspartic acid) (PASP), diethylenetriamine tetra(methylene phosphonic acid), diethylenetriamine pentakis(methylene phosphonic acid), 2-phosphonobutane-1,2,4-tricarboxylic acid, polyacrylic acid (PAA), phosphinocarboxylic acid (PPCA), diglycolamine phosphonate (DGA phosphonate), 1-hydroxyethylidene-1,1-diphosphonate (HEDP phosphonate), bisaminoethylether phosphonate (BAEE phosphonate), 2-acrylamido-2-methyl-1-propanesulphonic acid (AMPS), acrylic acid-hydroxypropyl acrylate copolymer, hydrolyzed poly(maleic anhydride) (HPMA), hydrolyzed maleic anhydride-acrylic acid copolymer (hydrolyzed, MA/AA), and acrylic acid-2-acrylamino-2-methylpropane sulfonic acid copolymer (AA/AMPS).

15. The method of claim 1 , wherein the compression wave is produced by an explosion.

16. The method of claim 15 , wherein the explosion is produced by a detonator, a primer, or a detonatable material placed downhole in the subterranean formation.

17. The method of claim 1 , wherein the compression wave is sent from a surface, down a wellbore, and to the cocrystals in the subterranean formation.

18. A method of treating a subterranean formation, the method comprising:
placing in the subterranean formation a composition comprising:
cocrystals, each cocrystal independently comprising:
a scale-inhibiting compound; and
a secondary material, wherein the scale-inhibiting compound and the secondary material are present in the cocrystal at a mole ratio of about 1:0.01 to about 1:100; and
a crosslinker compound comprising at least one of chromium, aluminum,

Assignees

• Halliburton Energy Services Inc

Inventors

• Holtsclaw Jeremy A
• Schultheiss Nathan Carl

Classifications

• C04B20/0048

  Fibrous materials · CPC title

• C09K8/467

  containing additives for specific purposes · CPC title

• E21B37/06 Primary

  using chemical means for preventing or limiting {, e.g. eliminating,} the deposition of paraffins or like substances · CPC title

• C09K8/528 Primary

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

• C04B24/2652

  Nitrogen containing polymers, e.g. polyacrylamides, polyacrylonitriles · CPC title