Method of improving the permeability of an underground petroleum-containing formation

• US 6,972,274 B1
• Filed: 09/15/2000
• Issued: 12/06/2005
• Est. Priority Date: 09/24/1999
• Status: Expired due to Term

• Current Assignee: Nouryon Chemicals International B.V. (Nouryon BV)
• Original Assignee: Akzo Nobel N.V. (Nouryon BV)
• Inventors: Slikta, Alberto, Johnson, Andress K., Gadberry, James F.
• Primary Examiner(s): Tucker, Philip C.
• Application Number:
  US10/088,962
• Time in Patent Office: 1,908 Days
• Field of Search: 507/211, 507/240, 507/261, 507/244, 507/246, 166/305.1, 166/307, 166/311, 166/270, 166/270.1
• US Class Current: 507/240
• CPC Class Codes: C09K 8/52 Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning
• CPC Class Codes: C09K 8/584 characterised by the use of specific surfactants
• CPC Class Codes: C09K 8/602 containing surfactants
• CPC Class Codes: F16L 19/00 Joints in which sealing surfaces are pressed together by means of a member, e.g. a swivel nut, screwed on or into one of the joint parts screw-threaded joints F16L15/00; F16L17/00 takes precedence; if using bolts or equivalent connecting means F16L23/00; electrically insulating F16L25/02; adjustable joints, joints allowing movement F16L27/00; specially adapted for pipes of brittle material F16L49/06

Abstract

The present invention generally relates to a method and a composition useful in restoring the permeability of a porous underground petroleum containing formation. Restoring permeability to the formation enhances the injectivity thereby accelerating petroleum recovery. The method of the invention comprises treating said formation with a composition which comprises a combination of at least one nonionic compound, preferably an alkoxylated alcohol, with at least one cationic compound, preferably a quaternary ammonium compound, in an amount effective to improve the permeability of the formation. The composition may also optionally contain an alkyl glycoside.

Claims

1. A method for improving the water injectivity of an injection well in a petroleum containing formation by restoring the permeability of said petroleum-containing formation thereby enhancing the recovery of oil by the waterflood process, said method comprising treating said formation with a composition which comprises at least one nonionic surfactant and at least one cationic surfactant in an amount and a concentration effective to improve the permeability of said formation, wherein said at least one nonionic surfactant is selected from the group consisting of alkanolamides, alkoxylated alcohols, alkoxylated amines, alkyl phenyl polyethoxylates, lecithin, hydroxylated lecithin, fatty acid esters, glycerol esters and their ethoxylates, glycol esters and their ethoxylates, esters of propylene glycol, sorbitan, ethoxylated sorbitan polyglycosides and mixtures thereof, and said at least one cationic surfactant is an ethoxylated quaternary ammonium compound.

2. The method of claim 1 wherein said at least one nonionic surfactant is an ethoxylated linear or branched alcohol of the formula:

R—

O—

(CH₂CH₂O)_z—

H 

 

(I)

wherein R Is a C₈–

C₃₀ saturated or unsaturated, branched or straight chain alkyl, or alkylphenyl group of the formula

wherein A is a C₈–

C₃₀ saturated or unsaturated, branched or straight chain alkyl, preferably a C₉–

C₁₂ linear or branched alkyl, and z is an integer of from 1 to 30.

3. The method of claim 2 wherein A is a saturated or unsaturated, branched or straight chain C₉–

C₁₂ alkyl.

4. The method of claim 2 wherein said ethoxylated alcohol is selected from the group consisting of laury alcohol ethoxylated with 3 moles of ethylene oxide(EO), coco alcohol ethoxylated with 3 moles of EO, stearyl alcohol ethoxylated with 5 moles of EO, mixed C₁₂–

C₁₅ alcohol ethoxylated with 7 moles EO, mixed secondary C₁₁–

C₁₅ alcohol ethoxylated with 7 moles EO, mixed C₉–

C₁₁ linear alcohol ethoxylated with 6 moles EO, a C₉–

C₁₁ alcohol ethoxylated with 4 moles EO, and mixtures thereof.

5. The method of claim 1 wherein said at least one cationic surfactant is an ethoxylated quaternary ammonium compound of the general formula:

wherein R₁ is an saturated or unsaturated, branched or straight chain alkyl group having 8–

22 carbon atoms;

R₂ is a C₁ to C₆ alkyl group, 2-ethylhexyl, hydroxyethyl, hydroxypropyl;

R₃ is a group of the formula;

wherein R₅ and R₆ independently selected from hydrogen or a C₁ to C₆ alkyl group, and m+n is an integer of from 2–

80;

R₄ is selected from R₂ or R₃; and

X⁻

is an anion.

6. The method of claim 1 wherein said composition comprises a combination of

(i) at least one ethoxylated linear or branched alcohol having from 8 to 18 carbon atoms reacted with 2 to 12 moles of ethylene oxide;

(ii) at least one quaternary ammonium compound of the general formula;

wherein R₁ is an saturated or unsaturated, branched or straight chain alkyl group having 8–

22 carbon atoms;

R₂ is a C₁ to C₆ alkyl group, 2-ethylhexyl, hydroxyethyl, hydroxypropyl;

R₃ is a group of the formula;

wherein R₅ and R₆ independently selected from hydrogen or a C₁ to C₆ alkyl group, and m+n is an integer of from 2–

80;

R₄ is selected from R₂ or R₃; and

X⁻

is an anion, and

(iii) up to 30% by weight of at least one (poly) alkyl glucoside.

7. The method of claim 6 wherein said ethoxylated alcohol is selected from the group consisting of lauryl alcohol ethoxylated with 3 moles of ethylene oxide(EO), coco alcohol ethoxylated with 3 moles of EO, stearyl alcohol ethoxylated with 5 moles of EO, mixed C₁₂–

C₁₅ alcohol ethoxylated with 7 moles EO, mixed secondary C₁₁–

C₁₅ alcohol ethoxylated with 7 moles EO, mixed C₉–

C₁₁ linear alcohol ethoxylated with 6 moles EO, a C₉–

C₁₁ alcohol ethoxylated with 4 moles EO, and mixtures thereof.

8. The method of claim 6 wherein R₁ is Coco alkyl, m+n=15, R₂ is methyl, R₅ and R₆ are both H and X⁻

is Cl⁻

or methylsulfate.

9. The method of claim 6 wherein said quaternary ammonium compound is selected from the group consisting of stearyl methyl bis(ethoxy) ammonium chloride (12 moles EO), stearyl ethyl bis(ethoxy) ammonium ethyl sulfate (15 moles EO), tallow methyl bis(ethoxy) ammonium methyl sulfate (15 moles EO), tallow ethyl bis(ethoxy) ammonium methyl sulfate (15 moles EO), hydrogenated tallow methyl bis(ethoxy) ammonium chloride (15 moles EO), coco methyl bis (ethoxy) ammonium chloride (20 moles EO), and mixtures thereof.

10. The method of claim 6 wherein the HLB of the quaternary ammonium compound is from about 14.00 to 22.00.

11. The method of claim 6 wherein said composition additionally comprises up to 30% of a (poly) alkyl glycoside of formulae III or IV:

R₄(CH₂)_y—

O—

G_xH 

 

(III)

wherein R₄ is a straight or branched chain alkyl or alkenyl group having from 8 to 21 carbon atoms, G is a monosaccharide residue and x and y are selected from a number of from 1 to 5;

wherein R₄ is a straight or branched chain alkyl or alkenyl group having from 8 to 21 carbon atoms, R₅ is hydrogen or a straight or branched chain alkyl or alkenyl group having from 8 to 21 carbon atoms, G is a monosaccharide residue and x and y are selected from a number of from 1 to 5.

12. The method of claim 1 wherein said composition additionally comprises one or more solvents.

13. The method of claim 12 wherein said solvent is selected from the group consisting of water, lower alcohols, glycol ethers and mixtures thereof.

14. The method of claim 13 wherein said solvent is selected from the group consisting of methanol, ethanol, 1-propanol, 2-propanol and the like, glycols such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol, polyethylene glycol-polyethylene glycol block copolymers, and mixtures thereof.

15. The method of claim 1 wherein the ratio of said at least one nonionic surfactant to said at least one cationic surfactant is in the range of 4:

1 to 1;

4.

16. The method of claim 15 wherein said composition comprising said at least one nonionic surfactant to said at least one cationic surfactant is diluted to a concentration of from about 0.1% to about 10% by weight prior to injection into the formation.