IP Library Granted Patent US 8,017,562
Granted Patent B2
US 8,017,562 · App. 12/940,298 · Granted Sep 13, 2011

Gelled hydrocarbons for oilfield processes, phosphate ester compounds useful in gellation of hydrocarbons and methods for production and use thereof

Assignee: Brine-Add Fluids Ltd.
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Quick Facts
Patent No.
US 8,017,562
App. No.
12/940,298
Granted
Sep 13, 2011
Kind
B2
Abstract

Phosphate esters useful for gelling hydrocarbons in combination with a metal source are disclosed along with methods of preparation of the phosphate esters. Fouling in oil refinery towers has been attributed due to distillation of impurities present in phosphate esters used to gel hydrocarbons for oil well fracturing. The improved method of preparation of the phosphate ester results in a product that substantially reduces or eliminates volatile phosphorus, which is phosphorus impurities that distill up to 250° C., and increases the high temperature viscosity of the hydrocarbon gels formed using the phosphate esters.

Claims (51)

1. A method of treating a subterranean well comprising:

providing a hydrocarbon liquid;

gelling the hydrocarbon liquid to obtain a gelled hydrocarbon liquid by adding (i) a gelling agent including an asymmetric dialkyl phosphate ester having alkyl substituents differing in chain length by at least 4 atoms and (ii) a polyvalent metal cross linking agent, wherein any amount of phosphate triester that distills without decomposition at temperatures up to 250° C. is limited to less than or equal to 10 ppm phosphorus in the gelled hydrocarbon liquid;

introducing the gelled hydrocarbon liquid to a subterranean well; and

manipulating the gelled hydrocarbon liquid to treat a formation accessed by the subterranean well.

2. The method of claim 1 wherein the gelling agent further includes: a monoalkyl phosphate ester.

3. The method of claim 2 wherein the monoalkyl phosphate ester includes a monoalkyl group selected from the group consisting of: a straight chain alkyl having 5 to 20 carbon atoms and an alkoxyalkyl C n H (2n+1) O(CH 2 CH 2 O) x CH 2 CH 2 —, where n is about 6 to 16 and x is about 1 or 2.

4. The method of claim 3 wherein the monoalkyl phosphate ester content is less than 10% by weight of the gelling agent.

5. The method of claim 1 wherein the asymmetric dialkyl phosphate ester is according to the formula:

where the alkyl substituents of the asymmetric dialkyl phosphate ester are R 1 and R 2 , and:

R 1 is a straight chained alkyl group having 1 to 4 carbon atoms; and

R 2 is an alkyl group having 6 to 20 carbon atoms or an alkoxyalkyl group, C n H (2n+1) O(CH 2 CH 2 O) x CH 2 CH 2 —, where n is about 6 to 16 and x is about 1 or 2.

6. The method of claim 1 wherein the gelling agent further includes a symmetric phosphate diester having ester substituents greater than C5.

7. The method of claim 1 wherein the gelling agent includes 0 to 50% by weight of symmetric dialkyl phosphate ester with alkyl groups selected from the group consisting of an alkyl group having 6 to 20 carbon atoms and an alkoxyalkyl C n H (2n+1) O(CH 2 CH 2 O) x CH 2 CH 2 —, where n is about 6 to 16 and x is about 1 or 2; and 0 to 10% by weight of a monoalkyl phosphate ester where the monoalkyl group is selected from the group consisting of: a straight chain alkyl having 5 to 20 carbon atoms and an alkoxyalkyl C n H (2n+1) O(CH 2 CH 2 O) x CH 2 CH 2 —, where n is about 6 to 16 and x is about 1 or 2.

8. The method of claim 1 wherein the gelling agent includes asymmetric dialkyl phosphate ester according to formula [i] and at least one of the compounds of formula [ii] and [iii], the formulae being as follows:

wherein the alkyl substituents of the asymmetric dialkyl phosphate ester are R 1 and R 2 , and:

R 1 is a straight chained alkyl group having 1 to 4 carbon atoms; and

R 2 is an alkyl group having 6 to 20 carbon atoms or an alkoxyalkyl group, C n H (2n+1) O(CH 2 CH 2 O) x CH 2 CH 2 —, where n is about 6 to 16 and x is about 1 or 2; and

R 3 is a straight chain alkyl group having 5 to 20 carbon atoms or an alkoxyalkyl group C n H (2n+1) O(CH 2 CH 2 O) x CH 2 CH 2 —, where n is about 6 to 16 and x is about 1 or 2.

9. The method of claim 1 wherein the cross linking agent is based on aluminum (III), iron (III) or iron (II).

10. The method of claim 1 wherein manipulating includes pressuring up the gelled hydrocarbon liquid to fracture the formation.

11. The method of claim 1 wherein gelling the hydrocarbon liquid further includes adding one or more additives selected from: a proppant material, a non emulsifier or a delayed gel breaker effective to break the gelled hydrocarbon fluid over a given period of time.

12. A method of treating a subterranean well comprising:

gelling a hydrocarbon liquid to obtain a gelled hydrocarbon liquid by adding to the hydrocarbon liquid: (i) a gelling agent including an asymmetric dialkyl phosphate ester according to the formula:

R 1 is a straight chained alkyl group having 1 to 4 carbon atoms; and

R 2 is an alkyl group having 6 to 20 carbon atoms or an alkoxyalkyl group, C n H (2n+1) O(CH 2 CH 2 O) x CH 2 CH 2 —, where n is about 6 to 16 and x is about 1 or 2; and (ii) a polyvalent metal cross linking agent, wherein any amount of phosphate triester that distills without decomposition at temperatures up to 250° C. is limited to less than or equal to 10 ppm phosphorus in the gelled hydrocarbon liquid;

introducing the gelled hydrocarbon liquid to a subterranean well; and

manipulating the gelled hydrocarbon liquid to treat a formation accessed by the subterranean well.

13. A method of treating a subterranean well comprising:

gelling a hydrocarbon liquid to obtain a gelled hydrocarbon liquid by adding to the hydrocarbon liquid: (i) a gelling agent including an asymmetric dialkyl phosphate ester and a monoalkyl phosphate ester; and (ii) a polyvalent metal cross linking agent, wherein any amount of phosphate triester that distills without decomposition at temperatures up to 250° C. is limited to less than or equal to 10 ppm phosphorus in the gelled hydrocarbon liquid;

introducing the gelled hydrocarbon liquid to a subterranean well; and

manipulating the gelled hydrocarbon liquid to treat a formation accessed by the subterranean well.

14. The method of claim 13 wherein the monoalkyl phosphate ester includes a monoalkyl group selected from the group consisting of: a straight chain alkyl having 5 to 20 carbon atoms and an alkoxyalkyl C n H (2n+1) O(CH 2 CH 2 O) x CH 2 CH 2 —, where n is about 6 to 16 and x is about 1 or 2.

15. The method of claim 14 wherein the monoalkyl phosphate ester content is less than 10% by weight of the gelling agent.

16. A method of treating a subterranean well comprising:

gelling a hydrocarbon liquid to obtain a gelled hydrocarbon liquid by adding to the hydrocarbon liquid: (i) a gelling agent including an asymmetric dialkyl phosphate ester and a symmetric phosphate diester having ester substituents greater than C5; and (ii) a polyvalent metal cross linking agent, wherein any amount of phosphate triester that distills without decomposition at temperatures up to 250° C. is limited to less than or equal to 10 ppm phosphorus in the gelled hydrocarbon liquid;

introducing the gelled hydrocarbon liquid to a subterranean well; and

manipulating the gelled hydrocarbon liquid to treat a formation accessed by the subterranean well.

17. A method of treating a subterranean well comprising:

gelling a hydrocarbon liquid to obtain a gelled hydrocarbon liquid by adding to the hydrocarbon liquid: (i) a gelling agent including an asymmetric dialkyl phosphate ester according to formula [i] and at least one of the compounds of formula [ii] and [iii], the formulae being as follows:

wherein

R 1 is a straight chained alkyl group having 1 to 4 carbon atoms;

R 2 is an alkyl group having 6 to 20 carbon atoms or an alkoxyalkyl group, C n H (2n+1) O(CH 2 CH 2 O) x CH 2 CH 2 —, where n is about 6 to 16 and x is about 1 or 2;

R 3 is a straight chain alkyl group having 5 to 20 carbon atoms or an alkoxyalkyl group C n H (2n+1) O(CH 2 CH 2 O) x CH 2 CH 2 —, where n is about 6 to 16 and x is about 1 or 2; and in formula [i] the difference between the chain length of R 1 and the chain length of R 2 is greater than or equal to about 4 atoms, and; (ii) a polyvalent metal cross linking agent;

introducing the gelled hydrocarbon liquid to a subterranean well, wherein any amount of phosphate triester that distills without decomposition at temperatures up to 250° C. is limited to less than or equal to 10 ppm phosphorus in the gelled hydrocarbon liquid; and

manipulating the gelled hydrocarbon liquid to treat a formation accessed by the subterranean well.

18. A method of treating a subterranean well comprising:

gelling a hydrocarbon liquid to obtain a gelled hydrocarbon liquid by adding to the hydrocarbon liquid: (i) a gelling agent including an asymmetric dialkyl phosphate ester and (ii) a polyvalent metal cross linking agent, wherein any amount of phosphate triester that distills without decomposition at temperatures up to 250° C. is limited to less than or equal to 10 ppm phosphorus in the gelled hydrocarbon liquid;

introducing the gelled hydrocarbon liquid to a subterranean well; and

manipulating the gelled hydrocarbon liquid to treat a formation accessed by the subterranean well, wherein manipulating includes pressuring up the gelled hydrocarbon liquid to fracture the formation.

19. The method of claim 18 wherein gelling the hydrocarbon liquid further includes adding one or more of an additive selected from the group consisting of: a proppant material, a non emulsifier and a delayed gel breaker effective to break the gelled hydrocarbon fluid over a given period of time.

Assignments (2)
MERGER Recorded Jun 5, 2012
From: BRINE-ADD FLUIDS LTD.
To: ENGENIUM CHEMICALS CORP.
Reel/Frame 028317/0519 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2010
From: GHESNER, IOAN; HORTON, DAVID P.
To: BRINE-ADD FLUIDS LTD.
Reel/Frame 025327/0921 →
Continuity (4)
Division 12367841 · Feb 9, 2009
Provisional Application 61027342 · Feb 8, 2008
Provisional Application 61030040 · Feb 20, 2008
Related Publication 20110100633A1 · May 5, 2011