IP Library Granted Patent US 9,428,683
Granted Patent B2
US 9,428,683 · App. 13/829,495 · Granted Aug 30, 2016

Methods and compositions for stimulating the production of hydrocarbons from subterranean formations

Inventors: Randal M. Hill (The Woodlands, TX); Lakia M. Champagne (The Woodlands, TX); Nathan L. Lett (Cypress, TX); Maria Elizabeth Green (Conroe, TX); Hasnain Saboowala (The Woodlands, TX)
Assignee: Flotek Chemistry, LLC
C09K8/584C09K8/602C09K8/92
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Quick Facts
Patent No.
US 9,428,683
App. No.
13/829,495
Granted
Aug 30, 2016
Kind
B2
Abstract

Methods and compositions for stimulating of the production of hydrocarbons (e.g., formation crude oil and/or formation gas) from subterranean formations, and methods of selecting a composition for treating an oil or gas well. In some embodiments, the compositions are emulsions or microemulsions, which may include water, a terpene, and a surfactant.

Claims (20)

1. A method comprising:

selecting an emulsion or a microemulsion composition for injection into a wellbore of a well based on a determination of whether formation crude oil is produced or whether formation gas is produced by the well,

wherein, when formation crude oil is produced by the well, the emulsion or the microemulsion composition is selected to comprise a terpene having a phase inversion temperature greater than 43° C., water, and a surfactant and the ratio of water to terpene is between about 3:1 and about 1:2; and

wherein, when formation gas is produced by the well, the emulsion or the microemulsion is selected to comprise a terpene having a phase inversion temperature less than 43° C., water and a surfactant, and the ratio of water to terpene is between about 3:1 and about 1:2; and

injecting the emulsion or the microemulsion into the wellbore.

2. The method of claim 1 , further comprising injecting the emulsion or the microemulsion into the wellbore to increase production of formation crude oil or formation gas by the well.

3. The method of claim 1 , wherein the ratio of water to terpene is about 1:1.

4. The method of claim 1 , wherein the terpene is selected from the group consisting of linalool, geraniol, nopol, α-terpineol, menthol, eucalyptol, menthone, d-limonene, terpinolene, β-ocimene, γ-terpinene, α-pinene, and citronellene.

5. The method of claim 1 , wherein the emulsion or the microemulsion comprises a first type of terpene and a second type of terpene.

6. The method of claim 1 , wherein the emulsion or the microemulsion comprises a first type of surfactant and a second type of surfactant.

7. The method of claim 1 , wherein the surfactant is selected from the group consisting of alkyl polyglycol or alkyl polyglucoside nonionic surfactants, or mixtures of said nonionic surfactants with an ionic surfactant comprising anionic, cationic, or zwitterionic surfactants.

8. The method of claim 1 , wherein the emulsion or the microemulsion is diluted with an aqueous fluid prior to injection to the wellbore.

9. The method of claim 8 , wherein the emulsion or the microemulsion is diluted to between about 0.1 wt % and about 2 wt %.

10. The method of claim 8 , wherein the emulsion or the microemulsion is diluted to between about 0.2 wt % and about 0.4 wt %.

11. The method of claim 8 , wherein the emulsion or the microemulsion is diluted with water or brine.

12. The method of claim 1 , wherein the emulsion or the microemulsion further comprises a freezing point depression agent.

13. The method of claim 12 , wherein the emulsion or the microemulsion comprises a first type of freezing point depression agent and a second type of freezing point depression agent.

14. The method of claim 12 , wherein the freezing point depression agent comprises an alkylene glycol, an alcohol, and/or a salt.

15. The method of claim 12 , wherein the freezing point depression agent is present in an amount between about 5 wt % and about 40 wt %.

16. The method of claim 12 , wherein the surfactant is present in an amount between about 15 wt % and 55 wt %.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2016
From: SABOOWALA, HASNAIN
To: FLOTEK CHEMISTRY, LLC
Reel/Frame 039290/0379 →
CONVERSION Recorded Mar 21, 2016
From: CESI CHEMICAL, INC.
To: FLOTEK CHEMISTRY, LLC
Reel/Frame 038179/0131 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE NAME AND MIDDLE INITIAL OF INVENTOR CHAMPAGNE PREVIOUSLY RECORDED ON REEL 031976 FRAME 0567. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Aug 7, 2014
From: HILL, RANDAL M.; CHAMPAGNE, LAKIA M.; LETT, NATHAN L.; GREEN, MARIA ELIZABETH
To: CESI CHEMICAL, INC.
Reel/Frame 033492/0706 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2014
From: HILL, RANDAL M; CHAMPAGNE, LAKIA C; LETT, NATHAN L; GREEN, MARIA ELIZABETH
To: CESI CHEMICAL
Reel/Frame 031976/0567 →
Continuity (1)
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