IP Library Granted Patent US 10,913,884
Granted Patent B2
US 10,913,884 · App. 15/468,802 · Granted Feb 9, 2021

Temperature stability of polyols and sugar alcohols in brines

Inventors: Arthur G. Mack (Conroe, TX); Stanley Gunawan (The Woodlands, TX); Katrina Schultz (Spring, TX)
C09K8/035C09K8/06C09K8/62C09K8/665C09K8/68C09K8/845C09K8/86E21B21/00E21B43/04E21B43/26E21B43/267E21B47/00C09K2208/22
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,913,884
App. No.
15/468,802
Granted
Feb 9, 2021
Kind
B2
Abstract

A stabilized composition for use as a well fluid is provided. The stabilized composition includes a brine, a polyol, the polyol in an amount operable to inhibit solid formation, the polyol further operable to dissolve within the brine; and a stabilization compound, the stabilization compound operable to stabilize the polyol, such that the polyol does not degrade at a bottom hole temperature.

Claims (23)

1. A stabilized composition for use as a well fluid, the stabilized composition comprising:

a brine;

a polyol, the polyol present in an amount between 5 wt % and 30 wt % of the stabilized composition, where the amount of polyol is operable to inhibit solid formation, the amount of polyol further operable to dissolve within the brine, wherein the polyol is selected from the group consisting of a low-molecular weight polyalcohol, a sugar alcohol, and combinations thereof; and

a stabilization compound present at a concentration between 0.01 vol % to 3 vol % of the stabilized composition, where the concentration of the stabilization compound is operable to stabilize the polyol, such that the polyol does not degrade at a bottom hole temperature and the pH of the stabilized composition is maintained at the bottom hole temperature, wherein the bottom hole temperature is greater than 200° F., wherein the stabilization compound is an amine base wherein the stabilized composition is clear.

2. The stabilized composition of claim 1 , wherein the brine is a bromide-based brine.

3. The stabilized composition of claim 2 , wherein the bromide-based brine is selected from the group consisting of calcium bromide, sodium bromide, potassium bromide, magnesium bromide, ammonium bromide, and combinations thereof.

4. The stabilized composition of claim 1 , wherein the brine is a chloride-based brine.

5. The stabilized composition of claim 4 , wherein the chloride-based brine comprises calcium chloride, sodium chloride, potassium chloride, magnesium chloride, ammonium chloride, and combinations thereof.

6. The stabilized composition of claim 1 , wherein the brine is a combination of a bromide-based brine and a chloride-based brine.

7. The stabilized composition of claim 1 , wherein the polyol is the low-molecular weight polyalcohol selected from the group consisting of ethylene glycol, propylene glycol, glycerol, polyethylene glycols with molecular weights less than 800 daltons, and combinations thereof.

8. The stabilized composition of claim 1 , wherein the polyol is the sugar alcohol selected from the group consisting of sorbitol, xylitol, mannitol, threitol, arabitol, and combinations thereof.

9. The stabilized composition of claim 1 , wherein the amine base is selected from the group consisting of monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA), ethylenediamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), pentaethylenehexamine (PEHA), aminoethylpiperazine (AEP), ethyleneamine E-100, piperazine, diethylhydroxylamine (DEHA), diethylaminoethanol (DEAE), dimethylethanolamine (DMEA), methoxypropylamine (MOPA), morpholine, n-aminopropylmorpholine (APM), 4-[2-hydroxyethyl]morpholine, diglycolamine, N-[3-aminopropyl]diethanolamine, aminoethylethanolamine (AEEA), and combinations thereof.

10. A method of using the stabilized composition of claim 1 in a wellbore as the well fluid in a well activity, the method comprising the steps of:

introducing the stabilized composition into the wellbore,

and

engaging in the well activity in the wellbore.

11. The method of claim 10 , wherein the well activity is selected from the group consisting of completion activities, packer activities, workover activities, well intervention activities, well abandonment activities, well testing operations, displacement operations, gravel packing operations, frac packing, drilling operations, and fracturing operations.

12. The method of claim 10 , wherein the brine is a bromide-based brine, wherein the bromide-based brine comprises calcium bromide, sodium bromide, potassium bromide, and combinations thereof.

13. The method of claim 10 , wherein the brine is a chloride-based brine, wherein the chloride-based brine comprises calcium chloride, sodium chloride, potassium chloride, and combinations thereof.

14. The method of claim 10 , wherein the polyol is selected from the group consisting of a low-molecular polyalcohol, a sugar alcohol, and combinations thereof.

15. The method of claim 14 , wherein the polyol is the low-molecular weight polyalcohol selected from the group consisting of ethylene glycol, propylene glycol, glycerol, polyethylene glycols with molecular weights less than 800 daltons, and combinations thereof.

16. The method of claim 14 , wherein the polyol is the sugar alcohol selected from the group consisting of sorbitol, xylitol, mannitol, threitol, arabitol, and combinations thereof.

17. The method of claim 10 , wherein the stabilization compound is an amine base, wherein the amine base is selected from the group consisting of monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA), ethylenediamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), pentaethylenetetramine (PETA), pentaethylenehexamine (PEHA), aminoethylpiperazine (AEP), ethyleneamine E-100, piperazine, diethylhydroxylamine (DEHA), diethylaminoethanol (DEAE), dimethylethanolamine (DMEA), methoxypropylamine (MOPA), morpholine, n-aminopropylmorpholine (APM), 4-[2-hydroxyethyl]morpholine, diglycolamine, N-[3-aminopropyl]diethanolamine, aminoethylethanolamine (AEEA), and combinations thereof.

Assignments (7)
SECURITY INTEREST Recorded May 16, 2024
From: TETRA TECHNOLOGIES, INC.; TETRA PRODUCTION TESTING SERVICES, LLC
To: BANK OF AMERICA, N.A. (AS SUCCESSOR ADMINISTRATIVE AGENT TO JPMORGAN CHASE BANK, N.A.)
Reel/Frame 067454/0317 →
RELEASE OF SECURITY INTEREST Recorded Jan 18, 2024
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: TETRA TECHNOLOGIES, INC.; TETRA PRODUCTION TESTING SERVICES, LLC
Reel/Frame 066349/0878 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Jan 12, 2024
From: TETRA TECHNOLOGIES, INC.
To: SILVER POINT FINANCE, LLC
Reel/Frame 066295/0384 →
RELEASE OF SECURITY INTEREST Recorded Sep 19, 2018
From: JPMORGAN CHASE BANK, NATIONAL ASSOCIATION
To: TETRA TECHNOLOGIES, INC.
Reel/Frame 047112/0478 →
SECURITY INTEREST Recorded Sep 14, 2018
From: TETRA TECHNOLOGIES, INC.; TETRA PRODUCTION TESTING SERVICES, LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 047526/0436 →
SECURITY INTEREST Recorded Sep 11, 2018
From: TETRA TECHNOLOGIES, INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
Reel/Frame 046837/0040 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 3, 2017
From: MACK, ARTHUR G.; GUNAWAN, STANLEY; SCHULTZ, KATRINA
To: TETRA TECHNOLOGIES, INC.
Reel/Frame 042883/0866 →