Additives to reduce the crystallization temperature of brines and methods of use

US11001740B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11001740-B2
Application numberUS-201716468274-A
CountryUS
Kind codeB2
Filing dateJan 10, 2017
Priority dateJan 10, 2017
Publication dateMay 11, 2021
Grant dateMay 11, 2021

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A composition of a treatment fluid having an aqueous base fluid and a true crystallization temperature reduction additive. A method includes providing a treatment fluid having an aqueous base fluid, adding a true crystallization temperature reduction additive and placing the treatment fluid in a subterranean wellbore.

First claim

Opening claim text (preview).

What is claimed is: 1. An aqueous composition for use in a subterranean well comprising: an aqueous base fluid having a first true crystallization temperature; and a true crystallization temperature reduction additive that combined with the aqueous base fluid forms an aqueous composition having a second true crystallization temperature, the reduction additive comprising N-(phosphonomethyl)iminodiacetic acid (PMIDA); wherein the composition has a density of at least 14.2 lb/gal (1.70 kg/L) and the second true crystallization temperature is at least 9° F. (5° C.) less than the first true crystallization temperature. 2. The composition of claim 1 , wherein the aqueous base fluid is selected from the group consisting of: a calcium bromide brine, a calcium chloride brine, a manganese (II) bromide brine, and combinations thereof. 3. The composition of claim 1 , wherein the true crystallization temperature reduction additive is PMIDA reacted with aqueous sodium hydroxide and used as a di-sodium acetate salt. 4. The composition of claim 1 , wherein the composition has a density of at least 14.2 lb/gal (1.70 kg/L) and the second true crystallization temperature is at least 12° F. (6.7° C.) less than the first true crystallization temperature. 5. The composition of claim 1 , wherein the composition has a density of at least 14.2 lb/gal (1.70 kg/L) and the second true crystallization temperature is at least 15° F. (8.3° C.) less than the first true crystallization temperature. 6. The composition of claim 1 , wherein the composition has a density of at least 14.2 lb/gal (1.70 kg/L) and the second true crystallization temperature is at least 20° F. (11.1° C.) less than the first true crystallization temperature. 7. The composition of claim 1 , wherein the composition has a density of at least 14.2 lb/gal (1.70 kg/L) and the second true crystallization temperature is at least 25° F. (13.9° C.) less than the first true crystallization temperature. 8. The composition of claim 2 , wherein the composition has a density of at least 14.8 lb/gal (1.77 kg/L) and the second true crystallization temperature is at least 20° F. (11.1° C.) less than the first true crystallization temperature; and wherein the true crystallization temperature reduction additive is chosen from the group consisting of: tartaric acid, gluconic acid, citric acid, malic acid, and combinations thereof. 9. The composition of claim 1 , wherein the composition is zinc free. 10. The composition of claim 1 , wherein the composition is cesium free. 11. An aqueous composition for use in a subterranean well comprising: an aqueous base fluid having a first true crystallization temperature; and a true crystallization temperature reduction additive that combined with the aqueous base fluid forms an aqueous composition having a second true crystallization temperature, the reduction additive comprising N-(Phosphonomethyl)iminodiacetic acid (PMIDA); wherein the composition has a density of at least 14.2 lb/gal (1.70 kg/L) and the second true crystallization temperature is at least 9° F. (5° C.) less than the first true crystallization temperature; wherein the aqueous base fluid is selected from the group consisting of: a calcium bromide brine, a calcium chloride brine, a manganese (II) bromide brine, and combinations thereof. 12. The composition of claim 11 , wherein the composition is zinc free. 13. The composition of claim 11 , wherein the composition is cesium free. 14. A method comprising: providing an aqueous base fluid having a first true crystallization temperature; adding a true crystallization temperature reduction additive to the aqueous base fluid to form an aqueous composition having a second true crystallization temperature at least 9° F. (5° C.) less than the first true crystallization temperature, the reduction additive comprising N-(phosphonomethyl)iminodiacetic acid (PMIDA); and placing the aqueous composition in a subterranean well. 15. The method of claim 14 , further comprising performing a subterranean operation selected from the group comprising: drilling operations, lost circulation management operations, stimulation operations, sand control operations, perforating operations, completion operations, acidizing operations, scale inhibiting operations, water-blocking operations, clay stabilizer operations, fracturing operations, frac-packing operations, gravel packing operations, wellbore strengthening operations, sag control operations, displacing solids laden drilling fluid, and combinations thereof. 16. An aqueous composition for use in a subterranean well comprising: an aqueous base fluid having a first true crystallization temperature, the aqueous base fluid being selected from the group of: a calcium bromide brine, a calcium chloride brine, a manganese (II) bromide brine, and combinations thereof; and a true crystallization temperature reduction additive that combined with the aqueous base fluid forms an aqueous composition having a second true crystallization temperature, the reduction additive being formamide or urea; wherein the composition has a density of at least 14.2 lb/gal (1.70 kg/L) and the second true crystallization temperature is at least 9° F. (5° C.) less than the first true crystallization temperature. 17. The aqueous composition of claim 16 , wherein the reduction additive is present in a concentration of from 5% to 10% by weight of the aqueous composition. 18. An aqueous composition for use in a subterranean well comprising: an aqueous base fluid having a first true crystallization temperature, the aqueous base fluid being selected from the group of: a calcium bromide brine, a calcium chloride brine, a manganese (II) bromide brine, and combinations thereof; and a true crystallization temperature reduction additive that combined with the aqueous base fluid forms an aqueous composition having a second true crystallization temperature, the reduction additive being a hydroxy carboxylic acid and being present at a concentration of at least 10% to 45% by weight of the aqueous composition; wherein the composition has a density of at least 14.2 lb/gal (1.70 kg/L) and the second true crystallization temperature is at least 9° F. (5° C.) less than the first true crystallization temperature. 19. The composition of claim 18 , wherein the hydroxy carboxylic acid is chosen from the group consisting of: tartaric acid, gluconic acid, citric acid, malic acid, and combinations thereof. 20. The composition of claim 18 , wherein the hydroxy carboxylic acid is tartaric acid.

Assignees

Inventors

Classifications

  • containing inorganic compounds · CPC title

  • containing organic compounds · CPC title

  • Eroding chemicals, e.g. acids · CPC title

  • Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning · CPC title

  • containing organic compounds · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11001740B2 cover?
A composition of a treatment fluid having an aqueous base fluid and a true crystallization temperature reduction additive. A method includes providing a treatment fluid having an aqueous base fluid, adding a true crystallization temperature reduction additive and placing the treatment fluid in a subterranean wellbore.
Who is the assignee on this patent?
Halliburton Energy Serv Inc, Halliburton Energy Services Inc
What technology area does this patent fall under?
Primary CPC classification C09K8/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 11 2021 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 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).