Water-soluble polymers for oil recovery

• US 8,871,692 B2
• Filed: 01/26/2011
• Issued: 10/28/2014
• Est. Priority Date: 01/26/2010
• Status: Active Grant

• Current Assignee: SPCM SA
• Original Assignee: SPCM SA
• Inventors: Favero, Cdrick, Gaillard, Nicolas, Marroni, Dennis
• Primary Examiner(s): Chung, Susannah
• Assistant Examiner(s): Bhushan, Kumar R
• Application Number:
  US13/518,412
• Publication Number:
  US 20130072405A1
• Time in Patent Office: 1,371 Days
• US Class Current: 507/225
• CPC Class Codes: C09K 2208/28 Friction or drag reducing additives
• CPC Class Codes: C09K 8/035 Organic additives
• CPC Class Codes: C09K 8/12 containing synthetic organic macromolecular compounds or their precursors
• CPC Class Codes: C09K 8/588 characterised by the use of specific polymers polymeric surfactants C09K8/584
• CPC Class Codes: C09K 8/68 containing organic compounds

Abstract

The present invention refers to the use of anionic water-soluble polymers being partially or totally neutralized with an organic counter-ion for oil filed application, especially tertiary oil recovery steps.

Claims

1. A method of performing an oil field application comprising using a water-soluble polymer in the oil field application, wherein the water-soluble polymer is anionic, is partially or totally neutralized with at least one organic counter-ion, is obtainable from a polymerization mixture containing at least one non-ionic monomer and at least one anionic monomer, wherein more than 1% of the anionic groups present in the polymer are neutralized with said organic counter-ions, wherein the organic counter-ion is added before or during the polymerization of the polymerization mixture, and wherein at least one organic counter-ion is selected from the group consisting of ⁺NH₃(CH₃), ⁺NH₂(CH₃)₂, ⁺NH(CH₃)₃, ⁺NH₃(CH₂CH₃), ⁺NH₂(CH₂CH₃)₂, ⁺NH(CH₂CH₃)₃, ⁺NH₃(CH₂CH₂OH), ⁺NH₂(CH₂CH₂OH)₂, ⁺NH(CH₂CH₂OH)₃, methylbis(polyoxyethylene (15)) octadecyl quaternary ammonium, cations derived from N,N-Diethanolamine, N,N,N-triethanolamine, N-ethanolamine, N,N-di-isopropylamine, N,N-diethylamine, N,N-dipropylamine, N,N-dimethylaminopropylamine (DMAPA), N-propylamine, N-isopropylamine, N-isobutylamine, N,N-di-isobutylamine, N,N-dibutylamine and N-butylamine.

2. The method according to claim 1, wherein at least one organic counter-ion is selected from organic amines in the protonated form with the general formula ⁺NHR₁, R₂, R₃, wherein R₁ and R₂ independently from each other are selected from the group consisting of H, substituted or unsubstituted C1-C10alkyl, substituted or unsubstituted C3-C8cycloalkyl, substituted or unsubstituted C6-C14aryl, substituted or unsubstituted heteroaryl and polyoxyethylene-moieties, and R₃ is selected from the group consisting of substituted or unsubstituted C1-C10alkyl, substituted or unsubstituted C3-C8cycloalkyl, substituted or unsubstituted C6-C14aryl, substituted or unsubstituted heteroaryl and polyoxyethylene-moieties.

3. The method according to claim 1, wherein the at least one non-ionic monomer is a water-soluble vinylmonomer, preferably selected from the group consisting of acrylamide and methacrylamide, N-isopropyacrylamide, N,N-dimethylacrylamide, diacetone acrylamide, N-vinylformamide, N-vinyl acetamide, N-vinylpyridine, N-vinyl caprolactone and N-vinylpyrrolidone.

4. The method according to claim 1, wherein the at least one anionic monomer is selected from the group consisting of acrylic acid, methacrylic acid, itaconic acid, crotonic acid, maleic acid, fumaric acid, vinylsulfonic acid, vinylphosphonic acid, (meth)allylsulfonic acid, (meth)allylphosphonic acid, acrylamido methyl butanoic acid, acrylamido tertiary butyl sulfonic acid and water-soluble salts of the foregoing substances.

5. The method according to claim 1, wherein the polymerization mixture contains at least one cationic monomer, preferably a cationic monomer being derived from a non ionic monomer being protonated, more preferably a cationic monomer being derived from a non ionic monomer having a tertiary amine function including dimethylaminoethyl acrylate (DMAEA), dimethylaminoethyl methacrylate (DMAEMA), dimethylaminopropyl acrylate (DMAPA) and dimethylaminopropyl methacrylate (DMAPMA).

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

7. The method according to claim 1, wherein the polymerization mixture contains at least one branching agent, preferably at least one branching agent selected from the group consisting of methylene bisacrylamide (MBA), ethylene glycol diacrylate, polyethylene glycol dimethacrylate, vinyloxyethylacrylate or methacrylate, triallylamine, pentaerythritol triallyl ether, glycidylethers including diglycidylether, and epoxides.

8. The method according to claim 1, wherein the water-soluble anionic polymer in aqueous solution provides a filter ratio of not more than 1.5.

9. The method according to claim 1, wherein the anionicity of the water-soluble anionic polymer is less than 70 mol-%.

10. The method according to claim 1, wherein the weight average molecular weight of the water-soluble anionic polymer is more than 1 million and less than 20 million.

11. The method according to claim 1, wherein the oil field application is enhanced oil recovery, drilling, drag reduction, hydraulic fracturing, water shut-off and conformance control or mining.

12. The method according to claim 1, wherein the oil field application is a method for treating a subterranean formation.

13. The method according to claim 1, wherein the water-soluble anionic polymer in aqueous solution provides a filter ratio of not more than 1.3.

14. The method according to claim 1, wherein the water-soluble anionic polymer in aqueous solution provides a filter ratio of not more than 1.1.