Surfactant composition

US10196556B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10196556-B2
Application numberUS-201314402461-A
CountryUS
Kind codeB2
Filing dateMay 21, 2013
Priority dateMay 25, 2012
Publication dateFeb 5, 2019
Grant dateFeb 5, 2019

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

The invention provides a synergistic surfactant composition comprising: (a) from 5 to 95 wt % of a first surfactant which is selected from derivatives of alkyl polyglucosides and mixtures thereof; and (b) from 5 to 95 wt % of a second surfactant which is selected from: amphoteric surfactants, cationic surfactants, anionic surfactants, non-ionic surfactants, and mixtures thereof. This surfactant composition may be used to generate foam that is used for unloading a liquid from a hydrocarbon reservoir. It may be that the liquid unloading of foam generated using the surfactant composition is greater than that of foam generated from the first and second surfactants when they are foamed individually.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method of unloading liquid from a hydrocarbon reservoir, the method comprising: introducing two surfactants into the liquid, in order to foam the liquid; and then removing foamed liquid from the reservoir; wherein the first surfactant comprises an alkyl polyglucoside derivative selected from the group consisting of: Sodium hydroxypropyl sulfonate decyl glucose crosspolymer, Sodium hydroxypropyl sulfonate lauryl glucose crosspolymer, Disodium sulfosuccinate decyl glucoside crosspolymer, Disodium sulfosuccinate lauryl glucoside crosspolymer, Sodium succinate lauryl glucoside crosspolymer, Poly sodium decyl glucoside hydroxypropyl phosphate, Poly sodium lauryl glucoside hydroxypropyl phosphate, Coco glucoside betaine crosspolymer, Lauryl glucoside betaine crosspolymer, Hydroxypropyltrimonium coco glucosides chloride, and Stearvidimonium hydroxypropyl lauryl glucosides chloride, and the second surfactant is selected from the group consisting of: Lauramidopropyl hydroxysultaine, Cocamidopropyl hydroxysultaine, Lauramidopropyl betaine, Disodium lauramphodiacetate, and Disodium lauraminodipropionate. 2. The method of claim 1 , wherein the surfactants are used in the reservoir at a total active surfactant concentration of: (a) 100ppm or more; or (b) 150ppm or more; or (c) 250ppm or more; or (d) 500ppm or more; or (e) from 250ppm to 10,000ppm; or (f) from 500ppm to 5,000ppm. 3. The method according to claim 1 wherein the ratio of the first surfactant to the second surfactant by weight is: (a) from about 5:1 to about 1:5, or (b) from about 4:1 to about 1:4, or (c) from about 3:1 to about 1:3. 4. A method of unloading a liquid from a reservoir comprising the step of using a surfactant composition to generate a foam, wherein the composition comprises: a first surfactant which comprises an alkyl polyglucoside derivative selected from the group consisting of: Sodium hydroxypropyl sulfonate decvtglucose crosspolymer, Sodium hydroxypropyl sulfonate lauryl glucose crosspolymer, Disodium sulfosuccinate decyl glucoside crosspolymer, Disodium sulfosuccinate lauryl glucoside crosspolymer, Sodium succinate lauryl glucoside crosspolymer, Poly sodium decyl glucoside hydroxypropyl phosphate, Poly sodium lauryl glucoside hydroxypropyl phosphate, Coco glucoside betaine crosspolymer, Lauryl glucoside betaine crosspolymer, Hydroxypropyltrimonium coco glucosides chloride, and Stearylidimonium hydroxypropyl lauryl glucosides chloride; and a second surfactant which is selected from the group consisting of Lauramidopropyl hydroxysultaine, Cocamidopropyl hydroxysultaine, Lauramidopropyl betaine, Disodium lauramphodiacetate, and Disodium lauraminodipropionate. 5. A method of synergistically enhanced liquid unloading from a reservoir comprising a step of using two surfactants in combination, wherein the first surfactant comprises an alkyl polyglucoside derivative selected from the group consisting of: Sodium hydroxypropyl sulfonate decyl glucose crosspolymer, Sodium hydroxypropyl sulfonate lauryl glucose crosspolymer, Disodium sulfosuccinate decyl glucoside crosspolymer, Disodium sulfosuccinate lauryl glucoside crosspolymer, Sodium succinate lauryl glucoside crosspolymer, Poly sodium decyl glucoside hydroxypropyl phosphate, Poly sodium lauryl glucoside hydroxypropyl phosphate, Coco glucoside betaine crosspolymer, Lauryl glycoside betaine crosspolymer, Hydroxypropyltrimonium coco glucosides chloride,and Stearyldimonium hydroxypropyl lauryl glucosides chloride; and the second surfactant is selected from the group consisting of Lauramidopropyl hydroxysultaine, Cocamidopropyl hydroxysultaine, Lauramidopropyl betaine, Disodium lauramphodiacetate, and Disodium lauraminodipropionate. 6. The method of claim 5 , wherein the reservoir is a hydrocarbon reservoir.

Assignees

Inventors

Classifications

  • Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids · CPC title

  • Foams · CPC title

  • C09K8/584Primary

    characterised by the use of specific surfactants · CPC title

  • Anticorrosion additives · CPC title

  • characterised by the use of specific polymers {(polymeric surfactants C09K8/584)} · CPC title

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What does patent US10196556B2 cover?
The invention provides a synergistic surfactant composition comprising: (a) from 5 to 95 wt % of a first surfactant which is selected from derivatives of alkyl polyglucosides and mixtures thereof; and (b) from 5 to 95 wt % of a second surfactant which is selected from: amphoteric surfactants, cationic surfactants, anionic surfactants, non-ionic surfactants, and mixtures thereof. This surfactant…
Who is the assignee on this patent?
Rhodia Operations
What technology area does this patent fall under?
Primary CPC classification C09K8/584. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 05 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).