IP Library › Granted Patent US 8,813,843
Granted Patent B2
US 8,813,843 · App. 13/278,806 · Granted Aug 26, 2014

Hydrophobically modified polymer for thermally stabilizing fracturing fluids

Inventors: Giselle K. Braganza (Pune, IN); Achala V. Danait (Pune, IN)
Assignee: Halliburton Energy Services, Inc.
C09K8/685
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Quick Facts
Patent No.
US 8,813,843
App. No.
13/278,806
Granted
Aug 26, 2014
Kind
B2
Abstract

A method for treating a zone of subterranean formation is provided. The method includes the steps of: (a) forming a treatment fluid including: (i) water; (ii) a viscosity-increasing agent selected from the group consisting of water-soluble polysaccharides, water-soluble derivatives thereof, and any combination of the foregoing; (iii) a crosslinker for the viscosity-increasing agent; (iv) a hydrophobically modified water-soluble polymer; wherein the viscosity-increasing agent is not a hydrophobically modified polymer; and (b) introducing the treatment fluid into a zone of a subterranean formation, wherein the zone has a design temperature of equal to or greater than 350° F.

Claims (29)

1. A method for treating a zone of subterranean formation, the method comprising the steps of:

(a) forming a treatment fluid comprising:

(i) water;

(ii) a viscosity-increasing agent selected from the group consisting of a carboxyalkyl derivative of guar, a carboxyalkyl derivative of cellulose, and any combination of the foregoing;

(iii) a crosslinker for the viscosity-increasing agent;

(iv) a hydrophobically modified water-soluble polymer, wherein the hydrophobically modified water-soluble polymer is: (a) a reaction product of a hydrophilic polymer and a hydrophobic compound; or (b) prepared from a polymerization reaction of at least one hydrophilic monomer and at least one hydrophobically modified hydrophilic monomer; and

wherein the viscosity-increasing agent is not a hydrophobically modified polymer, and

(b) introducing the treatment fluid into a zone of a subterranean formation, wherein the zone has a design temperature of equal to or greater than 350° F.

2. The method according to claim 1 , wherein the crosslinker is selected from the group consisting of metal crosslinkers, borate crosslinkers, and any combination thereof.

3. The method according to claim 1 , wherein the viscosity-increasing agent and the crosslinker are each in at least a sufficient concentration such that a similar treatment fluid without the hydrophobically modified polymer would have a viscosity of at least 200 cP after 1 hour at 350° F.

4. The method according to claim 1 , wherein the hydrophobically modified water-soluble polymer comprises a polymer backbone comprising polar heteroatoms.

5. The method according to claim 1 , wherein the hydrophobically modified water-soluble polymer has a molecular weight in the range of about 100,000 to about 10,000,000.

6. The method according to claim 1 , wherein the hydrophobically modified water-soluble polymer is water soluble.

7. The method according to claim 1 , wherein the hydrophilic polymer comprises at least one polymer selected from the group consisting of: a cellulose, a chitosan, a polyamide, a polyetheramine, a polyethyleneimine, a polyhydroxyetheramine, a polylysine, a polysulfone, and a starch.

8. The method according to claim 1 , wherein the hydrophobic compound has an alkyl chain length of about 4 to about 22 carbons.

9. The method according to claim 1 , wherein the mole ratio of the hydrophilic monomer to the hydrophobically modified hydrophilic monomer in the hydrophobically modified water-soluble polymer is in the range of about 99.98:0.02 to about 90:10.

10. The method according to claim 1 , wherein the hydrophobically modified water-soluble polymer is a relative permeability modifier.

11. The method according to claim 1 , wherein the hydrophobically modified polymer increases the thermal stability of the treatment fluid at 350° F. compared to a similar fluid without the hydrophobically modified polymer.

12. The method according to claim 1 , wherein the hydrophobically modified polymer is in at least a sufficient concentration to increase the thermal stability of the treatment fluid by at least one hour at 350° F. compared to a similar fluid without the hydrophobic ally modified polymer.

13. The method according to claim 12 , wherein the hydrophobically modified polymer is in less than a sufficient concentration to increase the viscosity of the treatment fluid by more than two-fold measured after 1 hour at 350° F. compared to a similar fluid without the hydrophobically modified polymer.

14. The method according to claim 12 , wherein the hydrophobically modified polymer is in a concentration of less than 20% wt/vol of the water.

15. The method according to claim 1 , wherein the treatment fluid comprises: inorganic salt.

16. The method according to claim 1 , wherein the treatment fluid comprises: a breaker.

17. The method according to claim 1 , wherein the treatment fluid comprises: an oxygen scavenger.

18. The method according to claim 17 , wherein the oxygen scavenger comprises sodium thiosulfate.

19. The method according to claim 1 , wherein step of introducing the treatment fluid into a zone of a subterranean formation is at a pressure above the fracture pressure of the zone.

20. The method according to claim 1 , wherein the carboxyalkyl derivative of guar is selected from the group consisting of: carboxymethylguar, carboxymethylhydroxyethylguar, carboxymethylhydroxypropylguar, and ethylcarboxymethylguar, and any combination thereof.

21. The method according to claim 1 , wherein the carboxyalkyl derivative of cellulose is selected from the group consisting of: carboxymethylcellulose, carboxymethylhydroxyethylcellulose, ethylcarboxymethylcellulose, and any combination thereof.

22. The method according to claim 1 , wherein the hydrophilic polymer comprises at least one polymer selected from the group consisting of: a chitosan, a polyetheramine, a polyethyleneimine, a polyhydroxyetheramine, a polylysine, a polysulfone, and a starch.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2012
From: BRAGANZA, GISELLE K.; DANAIT, ACHALA V.
To: HALLIBURTON ENERGY SERVICES, INC.
Reel/Frame 028980/0489 →
Continuity (1)
Related Publication 20130098618A1 · Apr 25, 2013