IP Library Granted Patent US 9,702,218
Granted Patent B2
US 9,702,218 · App. 13/515,032 · Granted Jul 11, 2017

Use of elastomers to produce gels for treating a wellbore

Inventor: Donna Gerrard (Aberdeen, GB)
Assignee: M-1 Drilling Fluids U.K. Ltd.
E21B33/138C09K3/22C09K8/035C09K8/512C09K8/887C09K8/92C09K17/30
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Quick Facts
Patent No.
US 9,702,218
App. No.
13/515,032
Granted
Jul 11, 2017
Kind
B2
Abstract

A method of treating an earthen formation that includes introducing a first amount of a first blocked isocyanate in a liquid phase into the earthen formation; introducing a second amount of a second blocked isocyanate in a liquid phase into the earthen formation; the second blocked isocyanate group having a lower unblocking temperature than the first blocked isocyanate group; introducing at least one active hydrogen compound into the earthen formation; and contacting the first and second blocked isocyanates and the active hydrogen compound to form an elastomeric gel. The combination of two blocked isocyanates provides a synergistic effect so that the curing time can be optimised in a manner unexpected from the properties of the individual blocked isocyanates.

Claims (31)

1. A method of treating an earthen formation, comprising:

introducing a first amount of a first blocked isocyanate in a liquid phase into the earthen formation;

introducing a second amount of a second blocked isocyanate in a liquid phase into the earthen formation;

wherein the ratio of the volumes of the first blocked isocyanate to the second blocked isocyanate is within the range of 4:1 to 1:4;

wherein the second blocked isocyanate has a lower unblocking temperature than the first blocked isocyanate;

introducing at least one active hydrogen compound into the earthen formation; and

contacting the first and second blocked isocyanates and the active hydrogen compound to form an elastomeric gel, wherein the ratio of the first amount of the first blocked isocyanate to the second amount of the second blocked isocyanate is selected such that the second amount of the second blocked isocyanate added decreases the curing time of the formed elastomeric gel.

2. The method as claimed in claim 1 , wherein the first and second blocked isocyanates and the active hydrogen compound are injected simultaneously.

3. The method as claimed in claim 1 , wherein the first and second blocked isocyanates and the active hydrogen compound are injected sequentially.

4. The method as claimed in claim 1 , wherein the first and second blocked isocyanates independently comprise a backbone formed from at least one of a toluene diisocyanate (TDI) monomer unit and an isocyanurate (IPDI) monomer unit.

5. The method as claimed in claim 1 , wherein the first blocking group's unblocking temperature is between 110-150° C.

6. The method as claimed in claim 1 , wherein the unblocking temperature of the first and second blocked isocyanates are within 50° C. of each other.

7. The method as claimed in claim 1 , further comprising introducing at least one organometallic catalyst into the earthen formation.

8. The method as claimed in claim 1 , further comprising introducing at least one additive into the earthen formation selected from a group consisting of a plasticizer, a filler, a rheological additive, an accelerator, a retardant, and an adhesion promoter.

9. The method of claim 1 , wherein the treatment is at least one selected from a group consisting of wellbore strengthening treatments, loss control material treatments, water shutoff treatments, and zonal isolation treatments.

10. The method as claimed in claim 1 , wherein the first and second blocked isocyanates independently comprise a blocking group selected from a group consisting of methylethylcetoxime (MEKO), diethyl malonate (DEM) and dimethylpyrazole (DMP) and ε-Caprolactam.

11. The method as claimed in claim 10 , wherein the first and second blocked isocyanates independently include a blocking group selected from a group consisting of dimethyl pyrazole and ε-Caprolactam.

12. The method as claimed in claim 1 , wherein the first and second blocked isocyanates react with the active hydrogen compound to form one of polyurethanes and polyureas.

13. The method as claimed in claim 12 , wherein the first and second blocked isocyanates react with the active hydrogen compound comprising an amine to form a polyureas.

14. The method as claimed in claim 1 , wherein the first amount is greater than the second amount.

15. The method as claimed in claim 14 , wherein the second amount is 5-45 wt % of the total amount of the first and second blocked isocyanates.

16. The method as claimed in claim 15 , wherein the second amount is 10-20 wt % of the total amount of the first and second blocked isocyanates.

17. The method as claimed in claim 1 , wherein the first and second blocked isocyanates are mixed together before being introduced into the earthen formation.

18. The method as claimed in claim 17 , wherein the first and second blocked isocyanates and the active hydrogen compound are injected simultaneously.

19. The method as claimed in claim 17 , wherein the first and second blocked isocyanates and the active hydrogen compound are injected sequentially.

20. A method of treating an earthen formation, comprising:

introducing a first amount of a first blocked isocyanate in a liquid phase into the earthen formation;

introducing a second amount of a second blocked isocyanate in a liquid phase into the earthen formation;

wherein the second blocked isocyanate has at least a 10° C. lower unblocking temperature than the first blocked isocyanate;

introducing at least one active hydrogen compound into the earthen formation; and

contacting the first and second blocked isocyanates and the active hydrogen compound to form an elastomeric gel, wherein the ratio of the first amount of the first blocked isocyanate to the second amount of the second blocked isocyanate is selected such that the second amount of the second blocked isocyanate added decreases the curing time of the formed elastomeric gel.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2015
From: M-I L.L.C.
To: M-I DRILLING FLUIDS UK LTD
Reel/Frame 037029/0449 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2015
From: GERRARD, DONNA
To: M-I L.L.C.
Reel/Frame 037108/0973 →
Priority Claims (1)
GB 0921711.8 · Dec 11, 2009 · national
Continuity (1)
Related Publication 20140144637A1 · May 29, 2014