Stabilization and reduction of TCT of brines containing monovalent iodides

US10851278B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10851278-B2
Application numberUS-201715791872-A
CountryUS
Kind codeB2
Filing dateOct 24, 2017
Priority dateOct 24, 2017
Publication dateDec 1, 2020
Grant dateDec 1, 2020

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  5. First independent claim

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Abstract

Official abstract text for this publication.

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.

First claim

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What is claimed is: 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.

Assignees

Inventors

Classifications

  • C09K8/032Primary

    Inorganic additives · CPC title

  • containing organic compounds · CPC title

  • C09K8/06Primary

    Clay-free compositions (containing inorganic compounds only C09K8/05) · CPC title

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What does patent US10851278B2 cover?
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…
Who is the assignee on this patent?
Tetra Tech
What technology area does this patent fall under?
Primary CPC classification C09K8/032. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 10 related publications on this page (citations in our corpus or others sharing the same primary CPC).