IP Library Granted Patent US 10,851,278
Granted Patent B2
US 10,851,278 · App. 15/791,872 · Granted Dec 1, 2020

Stabilization and reduction of TCT of brines containing monovalent iodides

Inventors: Arthur G. Mack (Conroe, TX); Drew A. Fowler (Humble, TX)
Assignee: Tetra Technologies, Inc.
C09K8/06C09K8/032C09K8/575
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Quick Facts
Patent No.
US 10,851,278
App. No.
15/791,872
Granted
Dec 1, 2020
Kind
B2
Abstract

A composition for use in a wellbore activity, the composition comprising a stabilized monovalent iodide brine, the stabilized monovalent iodide brine comprises a monovalent salt system, the monovalent salt system comprises a monovalent iodide; a 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 monovalent iodide brine has a density greater than 10 lb/gal, where the stabilized monovalent iodide brine has a TCT of less than or equal to 70 deg F.

Claims (22)

1. A composition of a clear brine for use in a wellbore activity, the composition of a clear brine comprising:

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

a monovalent salt system, the monovalent salt system comprises a monovalent iodide;

a primary iodide stabilizer, an amount of primary iodide stabilizer operable to remove free iodine, prevent the formation of free iodine, and suppress TCT, wherein the primary iodide stabilizer comprises a low molecular weight polyol, wherein the amount of the primary iodide stabilizer is present in the range between 1 wt % and 30 wt % of the stabilized monovalent iodide brine;

a secondary iodide stabilizer, wherein the secondary iodide stabilizer is present in an amount in the range between 0.001% v/v and 5% v/v, wherein the amount of the secondary iodide stabilizer is operable to stabilize the primary iodide stabilizer, wherein the secondary iodide stabilizer is selected from the group consisting of amines, amino alcohols, hydroxylamines, hydrazines, erythorbic acid and erythorbate salts, ascorbic acid and ascorbate salts, citric acid and citrate salts, and combinations of the same,

wherein the amines are selected from the group consisting of ethylenediamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), pentaethylenehexamine (PEHA), aminoethylpiperazine (AEP), hexaethyleneheptamine (HEHA), piperazine, diethylhydroxylamine (DEHA), methoxypropylamine (MOPA), morpholine, n-aminopropylmorpholine (APM) and combinations thereof, wherein the amino alcohols are selected from the group consisting of monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA), diethylaminoethanol (DEAE), dimethylethanolamine (DMEA), aminoethylethanolamine (AEEA), 4-[2-hydroxyethyl] morpholine, diglycolamine, and combinations of the same; and

an aqueous fluid, the aqueous fluid present in the range between 20 wt % and 55 wt % of the stabilized monovalent iodide brine;

where the stabilized monovalent iodide brine has a density between 12.5 lb/gal and 16 lb/gal.

2. The composition of claim 1 , wherein the monovalent iodide is selected from the group consisting of lithium iodide, sodium iodide, potassium iodide, cesium iodide, rubidium iodide, and combinations of the same.

3. The composition of claim 1 , wherein the low molecular weight polyol is 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.

4. The composition of claim 1 , wherein the monovalent iodide is present in the range between 1 wt % and 70 wt %.

5. The composition of claim 1 , wherein the monovalent salt system further comprises an additional halide.

6. The composition of claim 5 , wherein the additional halide is selected from the group consisting of a divalent halide, a monovalent halide, and combinations of the same.

7. The composition of claim 5 , wherein the additional halide comprises a monovalent halide selected from the group consisting of lithium bromide, lithium chloride, sodium bromide, sodium chloride, potassium bromide, potassium chloride, cesium bromide, cesium chloride, rubidium bromide, rubidium chloride, and combinations of the same.

8. The composition of claim 5 , wherein the additional halide comprises a divalent halide selected from the group consisting of calcium bromide, calcium chloride, calcium iodide, magnesium bromide, magnesium chloride, magnesium iodide, strontium bromide, strontium chloride, strontium iodide, and combinations of the same.

9. The composition of claim 5 , wherein the monovalent iodide is present in the range between 1 wt % and 70 wt % of the stabilized monovalent iodide brine, and further wherein the additional halide is present in the range between 1 wt % and 45 wt %.

10. A method of creating a stabilized monovalent iodide clear brine, the method comprising the steps of:

adding an amount of a monovalent salt system to aqueous fluid, where the monovalent salt system comprises a monovalent iodide; and

adding an amount between 1 wt % and 30 wt % of a primary iodide stabilizer, wherein the primary iodide stabilizer comprises a low molecular weight polyol;

adding an amount between 0.001% v/v and 5% v/v of a secondary iodide stabilizer, wherein the secondary iodide stabilizer is selected from the group consisting of amines, amino alcohols, hydroxylamines, hydrazines, erythorbic acid and erythorbate salts, ascorbic acid and ascorbate salts, citric acid and citrate salts, and combinations of the same, wherein the amines are selected from the group consisting of ethylenediamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), pentaethylenehexamine (PEHA), aminoethylpiperazine (AEP), hex aethyleneheptamine (HEHA), piperazine, diethylhydroxylamine (DEHA), methoxypropylamine (MOPA), morpholine, n-aminopropylmorpholine (APM) and combinations thereof, wherein the amino alcohols are selected from the group consisting of monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA), diethylaminoethanol (DEAE), dimethylethanolamine (DMEA), aminoethylethanolamine (AEEA), 4-[2-hydroxyethyl]morpholine, diglycolamine, and combinations of the same.

11. The method of claim 10 , wherein the monovalent iodide is selected from the group consisting of lithium iodide, sodium iodide, potassium iodide, cesium iodide, rubidium iodide, and combinations of the same.

12. The method of claim 10 , wherein the monovalent salt system further comprises an additional halide.

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 043936/0736 →
Continuity (1)
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