Low dosage polymeric naphthenate inhibitors
View Patent ↗Polymeric naphthenate inhibitors are delivered into production fluids to contact mixtures of oil and water, such as in a hydrocarbon producing formation, production equipment, or processing systems. These polymeric naphthenate inhibitors exhibit surface-active properties causing the inhibitors to self-associate at oil-water interfaces and inhibit interactions between organic acids in the oil and cations or cation complexes in water. The large surface area makes these polymers persistent and effective at low concentrations. These compounds also inhibit aggregation of organic acid carboxylate salts that form when pH and pressure conditions are amenable to organic acid ionization. Preferred inhibitors do not form emulsions due to the formation of unstable mixed interface structures that result in coalescence of dispersed droplets. Naphthenate inhibitor dosages less than 100 ppm can effectively inhibit naphthenate salts or other organic acid salts that can form precipitates or emulsions during crude oil production or processing.
1. A method comprising:
contacting a surface active copolymer of an ester-acrylate monomer and a 2-Acrylamido-2-methylpropanesulfonic acid (AMPS) monomer, wherein the ester group of the ester-acrylate monomer comprises a straight or branched C 8 to C 18 alkyl group, with a mixture of divalent cation-containing water and naphthenic acid-containing oil at a dosage rate that is effective to self-associate at interfaces between the water and oil and inhibit formation of divalent cation salts of naphthenic acid, wherein the polymer is contacted with the mixture before a choke, manifold, turret, or a combination thereof, and wherein the pressure downstream of the choke, manifold, turret, or a combination thereof is reduced causing a release of carbon dioxide gas from the oil.
2. The method of claim 1 , wherein the naphthenic acid has an average molecular weight of between 200 and 1400 Daltons.
3. The method of claim 1 , wherein the divalent cation salts of the organic acid include naphthenate salts.
4. The method of claim 1 , wherein the polymer is a copolymer of the ester-acrylate and 2-Acrylamido-2-methylpropanesulfonic acid (AMPS) at a ratio between 9:1 and 1:9 to a molecular weight from 700 to 20,000 Dalton.
5. The method of claim 1 , wherein the dosage rate of the surface active polymer is less than 500 ppm.
6. The method of claim 1 , wherein the ester-acrylate monomer comprises 2-ethylhexyl acrylate.
7. A method comprising:
contacting a surface active polymer with a mixture of divalent cation-containing water and organic acid-containing oil at a dosage rate that is effective to self-associate at interfaces between the water and oil and inhibit formation of divalent cation salts of the organic acid, wherein the polymer is contacted with the mixture before a choke, manifold, turret, or a combination thereof, wherein the pressure downstream of the choke, manifold, turret, or a combination thereof is reduced causing a release of carbon dioxide gas from the oil, and wherein the polymer is a terpolymer of an ester-acrylate, 2-Acrylamido-2-methylpropanesulfonic acid (AMPS) and an unsaturated aromatic monomer reacted by free radical reaction at a ratio in between 8:1:1 and 1:8:1 and 1:1:8 having an average molecular weight from 700 to 20,000 Daltons and the unsaturated aromatic monomer is selected from styrene, divinylbenzene, or a combination thereof.
8. The method of claim 7 , wherein the ester group of the ester-acrylate monomer is a C 2 to C 18 alkyl group.
9. The method of claim 7 , wherein the ester group of the ester-acrylate monomer is a C 8 to C 18 alkyl group.
10. The method of claim 7 , wherein the ester-acrylate monomer comprises 2-ethylhexyl acrylate.
11. The method of claim 10 , wherein the unsaturated aromatic monomer comprises styrene.
12. The method of claim 10 , wherein the unsaturated aromatic monomer comprises divinylbenzene.
13. The method of claim 7 , wherein the unsaturated aromatic monomer comprises styrene.
14. The method of claim 7 , wherein the unsaturated aromatic monomer comprises divinylbenzene.
15. A method comprising:
contacting a surface active polymer with a mixture of divalent cation-containing water and organic acid-containing oil at a dosage rate that is effective to self-associate at interfaces between the water and oil and inhibit formation of divalent cation salts of the organic acid, wherein the polymer is contacted with the mixture before a choke, manifold, turret, or a combination thereof, and wherein the pressure downstream of the choke, manifold, turret, or a combination thereof is reduced causing a release of carbon dioxide gas from the oil, wherein the polymer is a copolymer of an ester-acrylate monomer and a 2-Acrylamido-2-methylpropanesulfonic acid (AMPS) monomer, and wherein the ester group of the ester-acrylate monomer comprises a straight or branched C 8 to C 18 alkyl group.