Corrosion inhibition treatment for aggressive fluids
US-2021164112-A1 · Jun 3, 2021 · US
US12570907B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12570907-B2 |
| Application number | US-202318525371-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 30, 2023 |
| Priority date | Nov 30, 2023 |
| Publication date | Mar 10, 2026 |
| Grant date | Mar 10, 2026 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A method for inhibiting corrosion in a refinery crude distillation unit includes introducing a corrosion inhibition composition to the refinery crude distillation unit. The corrosion inhibition efficiency of the corrosion inhibition composition may be at least 80%. The corrosion inhibition composition may include a carrier fluid and a corrosion inhibitor consisting essentially of a compound represented by Formula (I): where R 1 , R 2 , R 3 , and R 4 are each, independently, a hydrogen or an alkoxy group, and m and n are each, independently integers ranging from 2 to 10, wherein R 5 and R 6 are each, independently, a saturated C 6 -C 10 hydrocarbon group or an unsaturated C 6 -C 10 hydrocarbon group.
Opening claim text (preview).
What is claimed: 1 . A method for inhibiting corrosion in a refinery crude distillation unit, the method comprising: introducing a corrosion inhibition composition to the refinery crude distillation unit, wherein the corrosion inhibition composition comprises a carrier fluid and a corrosion inhibitor consisting essentially of a compound represented by Formula (I): where R 1 , R 2 , R 3 , and R 4 are each, independently, a hydrogen or an alkoxy group, and m and n are each, independently integers ranging from 2 to 10, wherein: at least one of R 1 , R 2 , R 3 , and R 4 is the alkoxy group; and R 5 and R 6 are each, independently, a saturated C 6 -C 10 hydrocarbon group or an unsaturated C 6 -C 10 hydrocarbon group, and wherein the corrosion inhibition efficiency of the corrosion inhibition composition is at least 80%. 2 . The method of claim 1 , wherein R 1 , R 2 , R 3 , and R 4 of the corrosion inhibition composition are each, independently, an ethoxy group. 3 . The method of claim 1 , wherein the corrosion inhibitor consisting essentially of a compound represented by Formula (I) is a reaction product derived from a fatty diamine and an epoxide. 4 . The method of claim 1 , wherein the corrosion inhibitor consists essentially of a compound represented by Formula (II): 5 . The method of claim 1 , further comprising measuring a corrosion inhibition efficiency of the corrosion inhibition composition in the presence of acidic brine prior to introducing the corrosion inhibition composition to the refinery crude distillation unit. 6 . The method of claim 1 , further comprising coating one or more inner surfaces of the refinery crude distillation unit. 7 . The method of claim 1 , further comprising: removing the corrosion inhibition from the composition; and feeding a crude hydrocarbon feedstock to the refinery crude distillation unit. 8 . The method of claim 7 , wherein the crude hydrocarbon feedstock is an acidic fluid comprising a mixture of components selected from at least one hydrocarbon, water, at least one organic acid, at least one inorganic acid, and an acid forming compound. 9 . The method of claim 1 , further comprising separating a crude hydrocarbon feedstock into one two or more fractions in a coated refinery crude distillation unit. 10 . The method of claim 1 , wherein the corrosion inhibition efficiency is at least 90%. 11 . The method of claim 1 , wherein the corrosion inhibition efficiency is measured in the presence of an acidic brine. 12 . The method of claim 1 , further comprising, prior to the introducing, preparing the corrosion inhibition composition. 13 . The method of claim 12 , further comprising, prior to preparing the corrosion inhibition composition, producing the corrosion inhibitor consisting essentially of a compound represented by Formula (I) by reacting ethylene oxide with a diamine represented by Formula (III): wherein R 5 and R 6 are each, independently, a saturated C 6 -C 10 hydrocarbon group or an unsaturated C 6 -C 10 hydrocarbon group. 14 . The method of claim 13 , wherein the diamine is Priamine™ 1074. 15 . The method of claim 13 , wherein the preparing the corrosion inhibition composition comprises dissolving the corrosion inhibitor in a range from 10 wt % to 50 wt % in the carrier fluid based on the total weight of the corrosion inhibition composition. 16 . The method of claim 1 , wherein the carrier fluid is selected from the group consisting of diesel, heavy aromatic naphtha, benzene, toluene, isopropyl alcohol, and combinations thereof.
containing a multiple nitrogen-to-carbon bond · CPC title
for minimising corrosion or incrustation · CPC title
Hydroxy amines · CPC title
Controlling or regulating · CPC title
Naphthenic acids, TAN · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.