IP Library Granted Patent US 11,021,645
Granted Patent B2
US 11,021,645 · App. 15/791,748 · Granted Jun 1, 2021

Stabilization and reduction of TCT of divalent iodide-containing brines

Inventors: Arthur G. Mack (Conroe, TX); Drew A. Fowler (Humble, TX)
C09K8/528C09K8/032C09K8/06C09K8/42E21B36/00
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 11,021,645
App. No.
15/791,748
Granted
Jun 1, 2021
Kind
B2
Abstract

A composition for use in a wellbore activity, the composition comprising a stabilized divalent iodide brine, the stabilized divalent iodide brine comprises a divalent salt system, where the divalent salt system comprises a divalent iodide, an primary iodide stabilizer, the primary iodide stabilizer operable to remove free iodine, prevent the formation of free iodine, and suppress TCT, and an aqueous fluid, where the stabilized divalent iodide brine has a density greater than 11 lb/gal, where the stabilized divalent iodide brines has a TCT of less than or equal to 70 deg F.

Claims (17)

1. A composition for use in a wellbore activity, the composition consisting essentially of:

a stabilized divalent iodide brine, the stabilized divalent iodide brine comprises:

a divalent salt system, the divalent salt system comprises a divalent iodide, wherein the divalent iodide is selected from the group consisting of calcium iodide, magnesium iodide, strontium iodide, and combinations of the same;

a primary iodide stabilizer, the primary iodide stabilizer operable to remove free iodine, prevent the formation of free iodine, and suppress true crystallization temperature (TCT), wherein the primary iodide stabilizer comprises a low molecular weight polyol selected from the group consisting of sorbitol, glycerol, xylitol, mannitol, diglycerol, polyethylene glycol with a molecular weight less than 1000 Da, and combinations of the same;

a secondary iodide stabilizer, the secondary iodide stabilizer operable to scavenge free oxygen or carbon dioxide and prevent oxidation of the iodide to iodine, the secondary iodide stabilizer selected from the group consisting of amines, amino alcohols, hydroxylamines, hydrazines, erythorbic acid and derivative erythorbate salts, ascorbic acid and derivative ascorbate salts, citric acid and derivative citrate salts, and combinations of the same;

and an aqueous fluid,

where the stabilized divalent iodide brine has a density greater than 11 lb/gal, and where the stabilized divalent iodide brine has a TCT of less than or equal to 70 deg F.

2. The composition of claim 1 , wherein the divalent iodide is present in the range between 1 wt % and 70 wt %, and further wherein the primary iodide stabilizer is present in the range between 0.1 wt % and 35 wt % of the stabilized divalent iodide brine.

3. The composition of claim 1 , wherein the secondary iodide stabilizer is present in the range between 0.001% v/v and 5% v/v.

4. The composition of claim 1 , where the secondary iodide stabilizer comprises an amine selected from the group consisting of ethylenediamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), pentaethylenehexamine (PEHA), aminoethylpiperazine (AEP), hexaethyleneheptamine (HEHA), piperazine, methoxypropylamine (MOPA), morpholine, n-aminopropylmorpholine (APM), and combinations of the same.

5. The composition of claim 1 , where the secondary iodide stabilizer comprises an amino alcohol selected from the group consisting of monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA), diethylaminoethanol (DEAE), dimethylethanolamine (DMEA), N-[3-aminopropyl]diethanolamine, aminoethylethanolamine (AEEA), 4-[2-hydroxyethyl]morpholine, diglycolamine, and combinations of the same.

6. The composition of claim 1 , where the secondary iodide stabilizer comprises an hydroxylamine selected from the group consisting of diethylhydroxylamine (DEHA), dimethylhydroxylamine (DMHA), hydroxylamine, and combinations of the same.

7. The composition of claim 1 , where the secondary iodide stabilizer comprises sodium erthyorbate.

8. The composition of claim 1 , where the secondary iodide stabilizer comprises a derivative ascorbate salt selected from the group consisting of sodium ascorbate, potassium ascorbate, magnesium ascorbate, calcium ascorbate and combinations of the same.

9. The composition of claim 1 , where the secondary iodide stabilizer comprises a derivative citrate salt selected from the group consisting of mono-, di-, and tri-sodium citrate, potassium citrate, magnesium citrate, calcium citrate, and combinations of the same.

10. The composition of claim 1 , where the secondary iodide stabilizer is selected form the group consisting of monoethanolamine (MEA), aminoethylethanolamine (AEEA), diethylhydroxylamine (DEHA), and combinations of the same.

11. The composition of claim 1 , wherein the divalent iodide is present in the range between 1 wt % and 70 wt %, and further wherein the primary iodide stabilizer is present in the range between 2 wt % and 25 wt % of the stabilized divalent iodide brine.

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 Oct 24, 2017
From: MACK, ARTHUR G.; FOWLER, DREW A.
To: TETRA TECHNOLOGIES, INC.
Reel/Frame 043935/0347 →
Continuity (1)
Related Publication 20190119556A1 · Apr 25, 2019