IP Library Granted Patent US 9,200,192
Granted Patent B2
US 9,200,192 · App. 13/889,709 · Granted Dec 1, 2015

Compositions and methods for enhancement of production of liquid and gaseous hydrocarbons

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Quick Facts
Patent No.
US 9,200,192
App. No.
13/889,709
Granted
Dec 1, 2015
Kind
B2
Abstract

A well treatment composition is well-designed for the simultaneous enhancement of the production of both liquid and gaseous hydrocarbons from the same reservoir on a non-selective basis. The well treatment composition includes a first surfactant and a second surfactant, wherein the second surfactant is selected from the group consisting of ethoxylated alkylene amines, ethoxylated alkyl amines, propoxylated alkylene amines, propoxylated alkyl amines, ethoxylated-propoxylated alkylene amines and ethoxylated-propoxylated alkyl amines. The well treatment composition also includes a first solvent, a second solvent and water. Methods for using the well treatment composition include the steps of emplacing the well treatment composition into wells having high and low gas-to-oil ratios.

Claims (50)

1. A method of treating a plurality of hydrocarbon-producing wells, wherein a first of the plurality of hydrocarbon-producing wells has a high gas-to-oil ratio and a second of the hydrocarbon-producing wells has a low gas-to-oil ratio, the method comprising the steps of:

providing a complex nanofluid additive;

emplacing the complex nanofluid additive into the first of the plurality of hydrocarbon-producing wells to lower the gas-to-oil ratio; and

emplacing the complex nanofluid additive into the second of the plurality of hydrocarbon-producing wells to raise the gas-to-oil ratio.

2. The method of claim 1 , wherein before the providing a complex nanofluid additive step, the method further comprises the steps of:

providing a first surfactant and a second surfactant, wherein the second surfactant is selected from the group consisting of ethoxylated alkylene amines, ethoxylated alkyl amines, propoxylated alkylene amines, propoxylated alkyl amines, ethoxylated-propoxylated alkylene amines and ethoxylated-propoxylated alkyl amines;

mixing the first surfactant with the second surfactant to form a surfactant mixture;

adding a first solvent and a second solvent to the surfactant mixture to form a solvent-surfactant mixture;

adding water to the solvent-surfactant mixture to form an emulsified solvent-surfactant mixture; and

adding the emulsified-solvent surfactant mixture to a carrier fluid to form the complex nanofluid additive.

3. The method of claim 2 , wherein the second surfactant is ethylenediaminealcoxylate.

4. The method of claim 2 , wherein the second surfactant is diethylenetriaminealcoxylate.

5. The method of claim 2 , wherein the first surfactant includes an ethoxylated alcohol.

6. The method of claim 5 , wherein the first surfactant includes an ethoxylated alcohol having between 8 and 18 carbon atoms and between 5 and 20 moles of ethylene oxide.

7. The method of claim 2 , wherein the second solvent is a co-solvent selected from the group consisting of short-chain alcohols and glycols.

8. The method of claim 2 , wherein the complex nanofluid additive comprises:

up to about 90% by volume of the first surfactant, wherein the first surfactant is selected from the group consisting of nonionic surfactants, cationic surfactants, and anionic surfactants;

up to about 16% by volume of the second surfactant, wherein the second surfactant is selected from the group consisting of ethylenediaminealcoxylate and diethylenetriaminealcoxylate;

up to about 10% by volume of the first solvent, wherein the first solvent is d-limonene; up to about 25% by volume of the second solvent, wherein the second solvent comprises a co-solvent or a mixture of co-solvents; and

up to about 30% by volume water.

9. The method of claim 1 , wherein before the providing a complex nanofluid additive step, the method further comprises the steps of:

providing a first surfactant and a second surfactant, wherein the second surfactant is selected from the group consisting of ethoxylated alkylene amines, ethoxylated alkyl amines, propoxylated alkylene amines, propoxylated alkyl amines, ethoxylated-propoxylated alkylene amines and ethoxylated-propoxylated alkyl amines;

mixing the first surfactant with the second surfactant to form a surfactant mixture;

adding a first solvent and a second solvent to the surfactant mixture to form a solvent-surfactant mixture; and

adding water to the solvent-surfactant mixture to form an emulsified solvent-surfactant mixture, wherein the emulsified solvent-surfactant mixture comprises a concentrated form of the complex nanofluid additive.

10. A method for increasing production of oil from a first well having a high gas-to-oil ratio and production of gas from a second well having a low gas-to-oil ratio, the method comprising the steps of:

providing a complex nanofluid additive;

emplacing the complex nanofluid additive into the first well; and

emplacing the complex nanofluid additive into the second well.

11. The method of claim 10 , wherein before the providing a complex nanofluid additive step, the method further comprises the steps of:

providing a first surfactant and a second surfactant, wherein the second surfactant is selected from the group consisting of ethoxylated alkylene amines, ethoxylated alkyl amines, propoxylated alkylene amines, propoxylated alkyl amines, ethoxylated-propoxylated alkylene amines and ethoxylated-propoxylated alkyl amines;

mixing the first surfactant with the second surfactant to form a surfactant mixture;

adding a first solvent and a second solvent to the surfactant mixture to form a solvent-surfactant mixture;

adding water to the solvent-surfactant mixture to form an emulsified solvent-surfactant mixture; and

adding the emulsified-solvent surfactant mixture to a carrier fluid to form the complex nanofluid additive.

12. The method of claim 11 , wherein the second surfactant is ethylenediaminealcoxylate.

13. The method of claim 11 , wherein the second surfactant is diethylenetriaminealcoxylate.

14. The method of claim 11 , wherein the first surfactant includes an ethoxylated alcohol.

15. The method of claim 11 , wherein the first surfactant includes an ethoxylated alcohol having between 8 and 18 carbon atoms and between 5 and 20 moles of ethylene oxide.

16. The method of claim 11 , wherein the second solvent is a co-solvent selected from the group consisting of short-chain alcohols and glycols.

17. The method of claim 11 , wherein the complex nanofluid additive comprises:

up to about 90% by volume of the first surfactant, wherein the first surfactant is selected from the group consisting of nonionic surfactants, cationic surfactants, and anionic surfactants;

up to about 16% by volume of the second surfactant, wherein the second surfactant is selected from the group consisting of ethylenediaminealcoxylate and diethylenetriaminealcoxylate;

up to about 10% by volume of the first solvent, wherein the first solvent is d-limonene; up to about 25% by volume of the second solvent, wherein the second solvent comprises a co-solvent or a mixture of co-solvents; and

up to about 30% by volume water.

18. The method of claim 10 , wherein before the providing a complex nanofluid additive step, the method further comprises the steps of:

providing a first surfactant and a second surfactant, wherein the second surfactant is selected from the group consisting of ethoxylated alkylene amines, ethoxylated alkyl amines, propoxylated alkylene amines, propoxylated alkyl amines, ethoxylated-propoxylated alkylene amines and ethoxylated-propoxylated alkyl amines;

mixing the first surfactant with the second surfactant to form a surfactant mixture;

adding a first solvent and a second solvent to the surfactant mixture to form a solvent-surfactant mixture; and

adding water to the solvent-surfactant mixture to form an emulsified solvent-surfactant mixture, wherein the emulsified solvent-surfactant mixture comprises a concentrated form of the complex nanofluid additive.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Apr 17, 2019
From: PNC BANK NATIONAL ASSOCIATION
To: CESI CHEMICAL, INC.
Reel/Frame 048916/0850 →
CONVERSION Recorded Mar 21, 2016
From: CESI CHEMICAL, INC.
To: FLOTEK CHEMISTRY, LLC
Reel/Frame 038188/0391 →
CONFIRMATORY ASSIGNMENT Recorded Aug 26, 2014
From: ZELENEV, ANDREI; CHAMPAGNE, LAKIA M.; ZHOU, BILL; LETT, NATHAN; DISMUKE, KEITH; PENNY, GLENN S.
To: CESI CHEMICAL, INC.
Reel/Frame 033616/0150 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2013
From: ZELENEV, ANDREI; CHAMPAGNE, LAKIA M.; ZHOU, BILL; LETT, NATHAN; DISMUKE, KEITH; PENNY, GLENN S.
To: CESI CHEMICAL, INC.
Reel/Frame 031366/0588 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 7, 2013
From: FLOTEK INDUSTRIES, INC.; CESI CHEMICAL, INC.; CESI MANUFACTURING, LLC; MATERIAL TRANSLOGISTICS, INC.; TELEDRIFT COMPANY; TURBECO, INC.; USA PETROVALVE, INC.; FLOTEK ACQUISITION INC.; FLORIDA CHEMICAL COMPANY, INC.
To: PNC BANK, NATIONAL ASSOCIATION
Reel/Frame 030569/0758 →