Solubility enhancers on basis of allyl alcohol for aqueous surfactant formulations for enhanced oil recovery

Patent metadata

Field	Value
Publication number	US-11225857-B2
Application number	US-201816627473-A
Country	US
Kind code	B2
Filing date	Jul 11, 2018
Priority date	Jul 14, 2017
Publication date	Jan 18, 2022
Grant date	Jan 18, 2022

Abstract

The present invention relates to a method for the production of crude oil from subterranean, oil-bearing formations comprising at least the following steps of providing an aqueous surfactant composition comprising water and a surfactant mixture, injecting said surfactant composition into the subterranean, oil-bearing formation through at least one injection well, thereby reducing the crude oil-water interfacial tension to less than 0.1 mN/m, and withdrawing crude oil from the formation through at least one production well, wherein the surfactant mixture comprises at least a surfactant (A) having the general formula R1—O—(CH2CH(R2)O)a—(CH2CH(CH3)O)b—(CH2CH2O)c—R3—Y−M+ (I) and a solubility enhancer (B) having the general formula R4—O—(CH2CH(CH3)O)x—(CH2CH2O)y—R3—Y−M+ (II), wherein R1 to R4, a, b, c, x, y, Y and M have the meaning as defined the the description and claims. The invention further relates to said aqueous surfactant composition and methods for preparing the same as well as the use of solubility enhancer (B) for enhancing the solubility of anionic surfactant (A).

First claim

The invention claimed is:

1. A method for the production of crude oil from subterranean, oil-bearing formations comprising at least the following steps:
(1) providing an aqueous surfactant composition comprising water and a surfactant mixture,
(2) injecting said surfactant composition into the subterranean, oil-bearing formation through at least one injection well, thereby reducing the crude oil-water interfacial tension to less than 0.1 mN/m, and
(3) withdrawing crude oil from the formation through at least one production well,
wherein the surfactant mixture comprises at least
(A) a surfactant (A) having the general formula
R 1 —O—(CH 2 CH(R 2 )O) a —(CH 2 CH(CH 3 )O) b —(CH 2 CH 2 O) c —R 3 —Y − M +   (I)

and
(B) a solubility enhancer (B) having the general formula
R 4 —O—(CH 2 CH(CH 3 O) x —(CH 2 CH 2 O) y —R 3 —Y − M +   (II),

wherein
R 1 is a hydrocarbon moiety having 8 to 36 carbon atoms,
R 2 is a hydrocarbon moiety having 2 to 16 carbon atoms,
R 3 is selected from the group of
a single bond,
an alkylene group —(CH 2 ) o —, wherein o is from 1 to 3,
a group —CH 2 —CH(OH)—CH 2 —,

R 4 is an allyl group H 2 C═CH—CH 2 —,
Y − is an anionic group selected from —COO − or —SO 3 − ,
M + is at least a cation selected from the group of alkali metal ions, NH 4 + , and organic ammonium ions,
a is a number from 0 to 69,
b is a number from 3 to 70,
c is a number from 0 to 50,
x is a number from 1 to 69,
Y is a number from 0 to 50,
and wherein
R 3 , Y − , and M + in (A) and (B) are identical,
x<b,
y=c, and
the molar proportion of surfactant (A)/solubility enhancer (B) is from 98:2 to 60:40.

2. The method according to claim 1 , wherein b is a number from 5 to 60.

3. The method according to claim 1 , wherein x is a number from 1 to 44.

4. The method according to claim 1 , wherein c is a number from 1 to 50, and y is a number from 1 to 50.

5. The method according to claim 1 , wherein a is 0.

6. The method according to claim 1 , wherein the sum of b and c is from 5 to 75.

7. The method according to claim 1 , wherein R 1 is a hydrocarbon moiety having 12 to 32 carbon atoms.

8. The method according to claim 1 , wherein Y − is a —COO − group and R 3 is —(CH 2 ) o — wherein o is from 1 to 3.

9. The method according to claim 1 , wherein Y − is an —SO 3 − group and R 3 is selected from —(CH 2 ) o — wherein o is 2 or 3 and —CH 2 —CH(OH)—CH 2 —.

10. The method according to claim 1 , wherein Y − is an —SO 3 − group and R 3 is a single bond or an alkylene group —(CH 2 ) o — wherein o is 1 to 3.

11. The method according to claim 1 , wherein the molar proportion of surfactant (A)/solubility enhancer (B) is from 95:5 to 65:35.

12. The method according to claim 1 , wherein the aqueous surfactant composition additionally comprises salts.

13. The method according to claim 1 , wherein the method is Winsor Type III microemulsion flooding.

14. An aqueous surfactant composition as defined in claim 1 .

15. A method of manufacturing a surfactant composition according to claim 14 comprising at least the following steps
(a) optionally alkoxylating an alcohol R 1 OH with alkylene oxides of the general formula

thereby obtaining R 1 —O—(CH 2 CH(R 2 )O) a H (VI),

(b) alkoxylating an alcohol R 1 OH or the alkoxylated alcohol R 1 —O—(CH 2 CH(R 2 )O) a H (VI) with propylene oxide, thereby obtaining a mixture of
R 1 —O—(CH 2 CH(R 2 )O) a —(CH 2 CH(CH 3 )O) b H  (V), and

R 4 —O—(CH 2 CH(CH 3 )O) x H  (VI),

(c) optionally alkoxylating the mixture of (V) and (VI) with ethylene oxide, thereby obtaining a mixture of
R 1 —O—(CH 2 CH(R 2 )O) a —(CH 2 CH(CH 3 )O) b (CH 2 CH 2 O) c H  (VII), and

R 4 —O—(CH 2 CH(CH 3 )O) x —(CH 2 CH 2 O) y H  (VIII),

(d) introducing terminal anionic groups —Y − M + into the mixture of (VII) and (VIII) thereby obtaining a mixture of
(A) a surfactant (A) having the general formula
R 1 —O—(CH 2 CH(R 2 )O) a —(CH 2 CH(CH 3 )O) b —(CH 2 CH 2 O) c —R 3 —Y − M +   (I)

and
(B) a solubility enhancer (B) having the general formula
R 4 —O—(CH 2 CH(CH 3 O) x —(CH 2 CH 2 O) y —R 3 —Y − M +   (II),

wherein R 1 , R 2 , R 3 , R 4 , Y − , M + , a, b, c, x, and y have the meaning as defined in claim 14 .

16. The method according to claim 15 , wherein the mixture of (VII) and (VIII) is reacted with an ω-halogenated carboxylic acid R 5 —(CH 2 ) o —COOH or a salt thereof, wherein R 5 is selected from F, Cl, Br, or I and o is from 1 to 3, thereby obtaining a mixture of
(A) a surfactant (A) having the general formula
R 1 —O—(CH 2 CH(R 2 )O) a —(CH 2 CH(CH 3 )O) b —(CH 2 CH 2 O) c —(CH 2 ) o —COO − M +   (Ia)

and
(B) a solubility enhancer (B) having the general formula
R 4 —O—(CH 2 CH(CH 3 )O) x —(CH 2 CH 2 O) y —(CH 2 ) o —COO − M +   (IIa).

17. A method for enchancing solubility of an anionic surfactant (A) of general formula (I)
R 1 —O—(CH 2 CH(R 2 )O) a —(CH 2 CH(CH 3 )O) b —(CH 2 CH 2 O) c —R 3 —Y − M +   (I)

which comprises utilizing a solubility enhancer (B) of general formula (II)
R 4 —O—(CH 2 CH(CH 3 O) x —(CH 2 CH 2 O) y —R 3 —Y − M +   (II),

wherein
R 1 is a hydrocarbon moiety having 8 to 36 carbon atoms,
R 2 is a hydrocarbon moiety having 2 to 16 carbon atoms,
R 3 is selected from the group of
a single bond,
an alkylene group —(CH 2 ) o —, wherein o is from 1 to 3,
a group —CH 2 —CH(OH)—CH 2 —,

R 4 is an allyl group H 2 C═CH—CH 2 —,
Y − is an anionic group selected from —COO − or —SO 3 − ,
M + is at least a cation selected from the group of alkali metal ions, NH 4 + , and organic ammonium ions,
a is a number from 0 to 69,
b is a number from 3 to 70,
c is a number from 0 to 50,
x is a number from 1 to 69,
Y is a number from 0 to 50.

18. The method as claimed in claim 17 , wherein
R 3 , Y − , and M + in (A) and (B) are identical,
x<b,
y=c, and
the molar proportion of surfactant (A)/solubility enhancer (B) is from 98:2 to 60:40.

Assignees

• Basf Se

Inventors

• Bittner Christian
• Oetter Guenter
• Tinsley Jack F
• Raths Hans-Christian
• Kienle Marcel Patrik
• Weisse Sebastian Alexander

Classifications

• C09K8/584 Primary

  characterised by the use of specific surfactants · CPC title

• E21B43/16 Primary

  Enhanced recovery methods for obtaining hydrocarbons · CPC title