A method of enhancing oil recovery in a subterranean reservoir is disclosed. In one embodiment, the method comprises providing a wellbore and a polymer suspension. The polymer suspension comprises a powder polymer having an average molecular weight of 0.5 to 30 Million Daltons suspended in a water s
A method of enhancing oil recovery in a subterranean reservoir is disclosed. In one embodiment, the method comprises providing a wellbore and a polymer suspension. The polymer suspension comprises a powder polymer having an average molecular weight of 0.5 to 30 Million Daltons suspended in a water soluble solvent having an HLB of greater than or equal to 8 and selected from a group, at a weight ratio of 20:80 to 80:20. The method comprises providing an aqueous fluid, mixing a sufficient amount of the polymer suspension in the aqueous fluid for the polymer to be hydrated resulting an injection solution in less than or equal to 4 hours, and injecting the injection solution into the wellbore. The injection solution contains a polymer concentration ranging from 100 ppm to 50,000 ppm and has a filter ratio of less than 1.5 at 15 psi using a 1.2 μm filter.
대표청구항▼
1. A method of enhancing oil recovery in a subterranean reservoir, the method comprising providing a wellbore in fluid communication with the subterranean reservoir;providing a polymer suspension, wherein the polymer suspension comprises a powder polymer having an average molecular weight of 0.5 to
1. A method of enhancing oil recovery in a subterranean reservoir, the method comprising providing a wellbore in fluid communication with the subterranean reservoir;providing a polymer suspension, wherein the polymer suspension comprises a powder polymer having an average molecular weight of 0.5 to 30 Million Daltons suspended in a water soluble solvent at a weight ratio of powder polymer to water soluble solvent ranging from 20:80 to 80:20, wherein the water soluble solvent has a HLB of greater than or equal to 8 and comprises a mixture of non-ionic and anionic surfactants, and wherein the polymer suspension contains less than or equal to 3 wt. % water;providing an aqueous fluid selected from any of surface water, water recovered from a production well, sea water, synthetic water, produced reservoir brine, reservoir brine, fresh water, produced water, water, saltwater, brine, synthetic brine, synthetic seawater brine, and mixtures thereof;mixing a sufficient amount of the polymer suspension in the aqueous fluid for the polymer to be hydrated resulting in an injection solution in less than or equal to 4 hours, the injection solution containing a polymer concentration ranging from 100 ppm to 50,000 ppm and having a filter ratio of less than 1.5 at 15 psi using a 1.2 μm filter;injecting the injection solution into the wellbore into the subterranean reservoir. 2. The method of claim 1, wherein the mixing of a sufficient amount of the polymer suspension in the aqueous fluid is via a mixing tank or an in-line mixer. 3. The method of claim 1, wherein the mixing of a sufficient amount of the polymer suspension in the aqueous fluid for the polymer to be hydrated resulting in an injection solution in less than or equal to 2 hours. 4. The method of claim 3, wherein the mixing of a sufficient amount of the polymer suspension in the aqueous fluid for the polymer to be hydrated resulting in an injection solution in less than or equal to 1 hour. 5. The method of claim 1, wherein the mixing of a sufficient amount of the polymer suspension in the aqueous fluid resulting in an injection solution having a filter ratio of less than or equal to 1.2 at 15 psi using a 1.2 μm filter. 6. The method of claim 5, wherein the mixing of a sufficient amount of the polymer suspension in the aqueous fluid resulting in an injection solution having a filter ratio of less than or equal to 1.05 at 15 psi using a 1.2 μm filter. 7. The method of claim 1, wherein the mixing of a sufficient amount of the polymer suspension in the aqueous fluid resulting in an injection solution having a turbidity of less than or equal to 20 NTU. 8. The method of claim 7, wherein the mixing of a sufficient amount of the polymer suspension in the aqueous fluid resulting in an injection solution having a turbidity of less than or equal to 15 NTU. 9. The method of claim 8, wherein the mixing of a sufficient amount of the polymer suspension in the aqueous fluid resulting in an injection solution having a turbidity of less than or equal to 10 NTU. 10. The method of claim 1, wherein after the powder polymer is suspended in the water soluble solvent for a period of at least 2 hours with a turbidity decrease of at least 25%. 11. The method of claim 10, wherein after the powder polymer is suspended in the water soluble solvent for a period of at least 2 hours with a turbidity decrease of at least 50%. 12. The method of claim 11, wherein after the powder polymer is suspended in the water soluble solvent for a period of at least 2 hours with a turbidity decrease of at least 75%. 13. The method of claim 1, wherein the mixing of a sufficient amount of the polymer suspension in the aqueous fluid is for less than or equal to 2 hours for an injection solution. 14. The method of claim 13, wherein the mixing of a sufficient amount of the polymer suspension in the aqueous fluid is for less than or equal to 1 hour for an injection solution. 15. The method of claim 1, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent for less than or equal to 24 hours, for a stable polymer suspension containing less than or equal to 3 wt. % water. 16. The method of claim 1, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent and wherein the powder polymer is a biopolymer that is a polysaccharide. 17. The method of claim 1, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent and wherein the powder polymer is a biopolymer or a synthetic polymer. 18. The method of claim 1, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent and wherein the powder polymer is a synthetic polymer selected from the group of polyacrylamides, partially hydrolyzed polyacrylamides, hydrophobically-modified associative polymers, copolymers of polyacrylamide and one or both of 2-acrylamido 2-methylpropane sulfonic acid and salts thereof and N-vinyl pyrrolidone, single-, co-, or ter-polymers of N-vinyl pyrrolidones, polyacrylic acid, polyvinyl alcohol, and mixtures thereof. 19. The method of claim 1, wherein the anionic surfactant is present in an amount of less than or equal to 5 wt. % as a stabilizer. 20. The method of claim 1, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent and wherein the water soluble solvent further comprises isopropyl alcohol (IPA), n-propyl alcohol, isobutyl alcohol (IBA), methyl-isobutyl alcohol, secondary butyl alcohol (SBA), ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, triethylene glycol monobutyl ether, and mixtures thereof. 21. The method of claim 1, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent and wherein the water soluble solvent is selected from ethoxylated surfactants, nonylphenol ethoxylates, alcohol ethoxylates, internal olefin sulfonates, isomerized olefin sulfonates, alkyl aryl sulfonates, medium alcohol (C10 to C17) alkoxy sulfates, alcohol ether [alkoxy]carboxylates, alcohol ether [alkoxy]sulfates, alkyl sulfonate, a-olefin sulfonates (AOS), dihexyl sulfosuccinates, alkylpolyalkoxy sulfates, sulfonated amphoteric surfactants, and mixtures thereof. 22. The method of claim 1, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent and wherein the water soluble solvent further comprises a co-solvent selected from the group of an ionic surfactant, non-ionic surfactant, anionic surfactant, cationic surfactant, nonionic surfactant, amphoteric surfactant, ketones, esters, ethers, glycol ethers, glycol ether esters, lactams, cyclic ureas, alcohols, aromatic hydrocarbons, aliphatic hydrocarbons, alicyclic hydrocarbons, nitroalkanes, unsaturated hydrocarbons, halocarbons, alkyl aryl sulfonates (AAS), a-olefin sulfonates (AOS), internal olefin sulfonates (IOS), alcohol ether sulfates derived from propoxylated Ci2-C2o alcohols, ethoxylated alcohols, mixtures of an alcohol and an ethoxylated alcohol, mixtures of anionic and cationic surfactants, disulfonated surfactants, aromatic ether polysulfonates, isomerized olefin sulfonates, alkyl aryl sulfonates, medium alcohol (C10 to C17) alkoxy sulfates, alcohol ether [alkoxy]carboxylates, alcohol ether [alkoxy]sulfates, primary amines, secondary amines, tertiary amines, quaternary ammonium cations, cationic surfactants that are linked to a terminal sulfonate or carboxylate group, alkyl aryl alkoxy alcohols, alkyl alkoxy alcohols, alkyl alkoxylated esters, alkyl polyglycosides, alkoxy ethoxyethanol compounds, isobutoxy ethoxyethanol (“iBDGE”), n-pentoxy ethoxyethanol (“n-PDGE”), 2-methylbutoxy ethoxyethanol (“2-MBDGE”), methylbutoxy ethoxyethanol (“3-MBDGE”), (3,3-dimethylbutoxy ethoxyethanol (“3,3-DMBDGE”), cyclohexylmethyleneoxy ethoxyethanol (hereafter “CHMDGE”), 4-Methylpent-2-oxy ethoxyethanol (“MIBCDGE”), n-hexoxy ethoxyethanol (hereafter “n-HDGE”), 4-methylpentoxy ethoxyethanol (“4-MPDGE”), butoxy ethanol, propoxy ethanol, hexoxy ethanol, isoproproxy 2-propanol, butoxy 2-propanol, propoxy 2-propanol, tertiary butoxy 2-propanol, ethoxy ethanol, butoxy ethoxy ethanol, propoxy ethoxy ethanol, hexoxy ethoxy ethanol, methoxy ethanol, methoxy 2-propanol and ethoxy ethanol, n-methyl-2-pyrrolidone, dimethyl ethylene urea, and mixtures thereof. 23. The method of claim 1, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent and wherein the weight ratio of powder polymer to water soluble solvent ranges from 30:70 to 70:30. 24. The method of claim 1, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent and wherein the weight ratio of powder polymer to water soluble solvent ranges from 30:70 to 70:30. 25. The method of claim 24, wherein the weight ratio of powder polymer to water soluble solvent ranges from 40:60 to 60:40. 26. The method of claim 1, wherein the wellbore is an injection wellbore associated with an injection well, and the method further comprising: providing a production well spaced apart from the injection well a predetermined distance and having a production wellbore in fluid communication with the subterranean reservoir,wherein the injection of the injection solution increases flow of hydrocarbons to the production wellbore. 27. The method of claim 1, wherein the wellbore is a hydraulic fracturing wellbore associated with a hydraulic fracturing well. 28. The method of claim 1, wherein the injection solution functions as a drag reducer. 29. The method of claim 1, wherein the injection solution is included in a hydraulic fracturing fluid. 30. A method of enhancing oil recovery in a subterranean reservoir, the method comprising injecting an injection solution into the subterranean reservoir, whereby the injection solution is prepared by mixing a powder polymer having an average molecular weight about 0.5 to 30 Million Daltons with a water soluble solvent at a weight ratio of powder polymer to water soluble solvent ranging from 20:80 to 80:20, generating a stable polymer suspension containing less than or equal to 3 wt. % water, wherein the water soluble solvent has a HLB of greater than or equal to 8 and comprises a mixture of non-ionic and anionic surfactants, and wherein the powder polymer is selected from the group of polyacrylamides, partially hydrolyzed polyacrylamides, hydrophobically-modified associative polymers, copolymers of polyacrylamide and one or both of 2-acrylamido 2-methylpropane sulfonic acid and salts thereof and N-vinyl pyrrolidone, single-, co-, or ter-polymers of N-vinyl pyrrolidones, polyacrylic acid, polyvinyl alcohol, biopolymers, synthetic polymers, and mixtures thereof;mixing a sufficient amount of the polymer suspension into an aqueous fluid for the polymer to be hydrated resulting in an injection solution containing a polymer concentration ranging from 100 ppm to 50,000 ppm in less than or equal to 4 hours;wherein the injection solution has a filter ratio of less than or equal to 1.5 at 15 psi using a 1.2 μm filter and a turbidity of less than or equal to 20 NTU. 31. The method of claim 1, wherein the water soluble solvent further comprises a glycol ether, an alcohol, a co-solvent, and mixtures thereof. 32. The method of claim 30, wherein the water soluble solvent further comprises a glycol ether, an alcohol, a co-solvent, and mixtures thereof. 33. The method of claim 1, wherein the non-ionic surfactant is selected from ethoxylated surfactants, nonylphenol ethoxylates, alcohol ethoxylates, and mixtures thereof; or wherein the anionic surfactant is selected from internal olefin sulfonates, isomerized olefin sulfonates, alkyl aryl sulfonates, medium alcohol (C10 to C17) alkoxy sulfates, alcohol ether [alkoxy]carboxylates, alcohol ether [alkoxy]sulfates, alkyl sulfonate, a-olefin sulfonates (AOS), dihexyl sulfosuccinates, alkylpolyalkoxy sulfates, sulfonated amphoteric surfactants, and mixtures thereof. 34. The method of claim 31, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent and wherein the water soluble solvent is selected from ethoxylated surfactants, nonylphenol ethoxylates, alcohol ethoxylates, internal olefin sulfonates, isomerized olefin sulfonates, alkyl aryl sulfonates, medium alcohol (C10 to C17) alkoxy sulfates, alcohol ether [alkoxy]carboxylates, alcohol ether [alkoxy]sulfates, alkyl sulfonate, a-olefin sulfonates (AOS), dihexyl sulfosuccinates, alkylpolyalkoxy sulfates, sulfonated amphoteric surfactants, and mixtures thereof. 35. The method of claim 31, wherein providing the polymer suspension comprises mixing the powder polymer into the water soluble solvent and wherein the water soluble solvent further comprises a co-solvent selected from the group of an ionic surfactant, non-ionic surfactant, anionic surfactant, cationic surfactant, nonionic surfactant, amphoteric surfactant, ketones, esters, ethers, glycol ethers, glycol ether esters, lactams, cyclic ureas, alcohols, aromatic hydrocarbons, aliphatic hydrocarbons, alicyclic hydrocarbons, nitroalkanes, unsaturated hydrocarbons, halocarbons, alkyl aryl sulfonates (AAS), a-olefin sulfonates (AOS), internal olefin sulfonates (IOS), alcohol ether sulfates derived from propoxylated Ci2-C2o alcohols, ethoxylated alcohols, mixtures of an alcohol and an ethoxylated alcohol, mixtures of anionic and cationic surfactants, disulfonated surfactants, aromatic ether polysulfonates, isomerized olefin sulfonates, alkyl aryl sulfonates, medium alcohol (C10 to C17) alkoxy sulfates, alcohol ether [alkoxy]carboxylates, alcohol ether [alkoxy]sulfates, primary amines, secondary amines, tertiary amines, quaternary ammonium cations, cationic surfactants that are linked to a terminal sulfonate or carboxylate group, alkyl aryl alkoxy alcohols, alkyl alkoxy alcohols, alkyl alkoxylated esters, alkyl polyglycosides, alkoxy ethoxyethanol compounds, isobutoxy ethoxyethanol (“iBDGE”), n-pentoxy ethoxyethanol (“n-PDGE”), 2-methylbutoxy ethoxyethanol (“2-MBDGE”), methylbutoxy ethoxyethanol (“3-MBDGE”), (3,3-dimethylbutoxy ethoxyethanol (“3,3-DMBDGE”), cyclohexylmethyleneoxy ethoxyethanol (hereafter “CHM DGE”), 4-Methylpent-2-oxy ethoxyethanol (“MIBCDGE”), n-hexoxy ethoxyethanol (hereafter “n-HDGE”), 4-methylpentoxy ethoxyethanol (“4- MPDGE”), butoxy ethanol, propoxy ethanol, hexoxy ethanol, isoproproxy 2-propanol, butoxy 2-propanol, propoxy 2-propanol, tertiary butoxy 2-propanol, ethoxy ethanol, butoxy ethoxy ethanol, propoxy ethoxy ethanol, hexoxy ethoxy ethanol, methoxy ethanol, methoxy 2-propanol and ethoxy ethanol, n-methyl-2-pyrrolidone, dimethyl ethylene urea, and mixtures thereof.
연구과제 타임라인
LOADING...
LOADING...
LOADING...
LOADING...
LOADING...
이 특허에 인용된 특허 (34)
Christensen Scott Patrick ; Keen Brian T., Aqueous resin compositions.
Beck Donald (Ledyard CT) Miller James W. (Mystic CT) Wernau William C. (Groton CT) Young ; III Thomas B. (North Stonington CT), Biopolymer compositions having enhanced filterability.
Pinschmidt ; Jr. Robert K. (1033 N. Glenwood St. Allentown PA 18104) Lai Ta-Wang (401 Ignacio Blvd. ; Apt. 133 Novato CA 94949), Enhanced oil recovery with high molecular weight polyvinylamine formed in-situ.
Chapman Richard George,GB2 ; Hazel Nicholas John,GB2 ; Stewart Nevin John,GB2 ; Goodwin Stephen Paul,GB2 ; Lucy Andrew Richard,GB2, Ether cosolvents for resin formulations.
Gregoli Armand A. (Tulsa OK) Olah Andrew M. (Spencer OH) Hamshar John A. (Owasso OK) Rimmer Daniel P. (Broken Arrow OK), In situ application of high temperature resistant surfactants to produce water continuous emulsions for improved crude r.
Chapman Richard George (Weybridge GB2) Collins Ian Ralph (Hampton GB2) Goodwin Stephen Paul (London GB2) Lucy Andrew Richard (York GB2) Stewart Nevin John (Guildford GB2), Oil and gas field chemicals.
Pirri Rosangela (Montardon FRX) Huet Yves (Carentan FRX) Donche Alain (Jurancon FRX), Process for improving the dispersibility and filterability of scleroglucan powders.
Lorenz Donald H. (Basking Ridge NJ) Williams Earl P. (Pen Argyl PA) Schultz Herman S. (Lexington MA), Process for increasing molecular weight of vinylpyrrolidone polymer.
Bittner, Christian; Oetter, Günter; Tinsley, Jack; Spindler, Christian; Alvarez Jürgenson, Gabriela; Vogel, Sophie, Process for tertiary mineral oil production using surfactant mixtures.
Buckman John D. (Memphis TN) Hunter Wood E. (Memphis TN) Pera John D. (Memphis TN) Taylor Robert M. (Memphis TN), Water-soluble dispersions of high molecular water-soluble polymers containing a surfactant and a water-soluble organic c.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.