Phosphorus functional inversion agents for water-in-oil latices and methods of use
US-2017037300-A1 · Feb 9, 2017 · US
US2016333252A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016333252-A1 |
| Application number | US-201615152833-A |
| Country | US |
| Kind code | A1 |
| Filing date | May 12, 2016 |
| Priority date | May 13, 2015 |
| Publication date | Nov 17, 2016 |
| Grant date | — |
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Invertible latices suitable for use in enhanced oil recovery are formed by adding a first inversion surfactant and a second inversion surfactant to a water-in-oil latex comprising about 15 wt % to 50 wt % of a water soluble polymer having a net ionic charge. The first inversion surfactant has a hydrophilic/lipophilic balance of about 15 to 35 and an ionic charge that is the opposite of the net ionic charge of the polymer. The second inversion surfactant has a hydrophilic/lipophilic balance of between about 8 and 20. The invertible latices are diluted in a single step to provide dilute latices having 10,000 ppm or less polymer solids.
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1 . An invertible latex comprising a water-in-oil latex comprising about 15 wt % to 50 wt % of a water soluble polymer having at least about 50 mole % acrylamide content, about 0.1 wt % to 2.0 wt % of a first inversion surfactant having a hydrophilic/lipophilic balance of about 15 to 35; and about 0.2 wt % to 4.0 wt % of a second inversion surfactant having a hydrophilic/lipophilic balance of between about 8 and 20. 2 . The invertible latex of claim 1 wherein the first inversion surfactant comprises a quaternary ammonium surfactant. 3 . The invertible latex of claim 2 wherein the quaternary ammonium surfactant comprises N,N-bis [polyoxyethylene]-methyloctadecylammonium chloride with a total of about 15 ethylene oxide units divided between two polyglycol substituents on the nitrogen. 4 . The invertible latex of claim 1 wherein the second inversion surfactant is nonionic. 5 . The invertible latex of claim 4 wherein the second inversion surfactant comprises an alkoxylated alcohol. 6 . The invertible latex of claim 3 wherein the alkoxylated alcohol comprises a linear or branched C 13 chain. 7 . The invertible latex of claim 1 wherein the invertible latex is shelf stable. 8 . The invertible latex of claim 1 wherein the water-in-oil latex further comprises about 10 wt % to 50 wt % water; about 15 wt % to 30 wt % of a compound or blend thereof that is less than 0.1 wt % soluble in water at 25° C. and is substantially a liquid over the range of 20° C. to 100° C. and comprising linear, branched, or cyclic hydrocarbon moieties; and about 5 wt % or less of emulsifying latex emulsifying surfactant characterized as a nonionic surfactant having a combined hydrophilic/lipophilic balance of between about 2 and 10. 9 . A method of forming an invertible latex, the method comprising a) forming a water-in-oil latex comprising about 15 wt % to 50 wt % of a water soluble polymer having at least 50 mole % acrylamide content, about 10 wt % to 50 wt % water, about 15 wt % to 30 wt % of a compound or blend thereof that is less than 0.1 wt % soluble in water at 25° C. and is substantially a liquid over the range of 20° C. to 100° C. and comprising linear, branched, or cyclic hydrocarbon moieties; and about 5 wt % or less of latex emulsifying surfactant characterized as having a combined hydrophilic/lipophilic balance of between 2 and 10, b) adding to the latex about 0.1 wt % to 2.0 wt % based on total latex weight of a first inversion surfactant having an HLB of about 15 to 35 and an ionic charge, to form an intermediate latex; and c) adding to the intermediate latex about 0.2 wt % to 4.0 wt % of a second inversion surfactant having an HLB of between about 8 and 20 to form an invertible latex. 10 . The method of claim 9 wherein the invertible latex is shelf stable. 11 . The method of claim 9 wherein the first inversion surfactant is added as an aqueous solution, the aqueous solution comprising about 10 wt % to 50 wt % of the first inversion surfactant. 12 . A method of recovering hydrocarbon compounds from a subterranean reservoir, the method comprising a) forming an invertible latex of claim 1 , b) adding a water source to the invertible latex in a single addition to form a dilute latex comprising about 100 ppm to 10,000 ppm of the polymer, c) injecting the dilute latex into the subterranean reservoir, and d) recovering the hydrocarbon compounds. 13 . The method of claim 13 wherein the water source is a high temperature water source. 14 . The method of claim 13 wherein the water source is a high total dissolved solids water source. 15 . The method of claim 13 wherein the water source is a high temperature, high total dissolved solids water source.
Homopolymers or copolymers of acrylamide or methacrylamide · CPC title
characterised by the use of specific polymers {(polymeric surfactants C09K8/584)} · CPC title
characterised by the use of specific surfactants · CPC title
Homopolymers or copolymers of acrylamide or methacrylamide · CPC title
Enhanced recovery methods for obtaining hydrocarbons · CPC title
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