Inhibiting corrosion in gas wells
US-2023002666-A1 · Jan 5, 2023 · US
US11959016B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11959016-B2 |
| Application number | US-202117347952-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 15, 2021 |
| Priority date | Jun 15, 2021 |
| Publication date | Apr 16, 2024 |
| Grant date | Apr 16, 2024 |
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 composition for inhibiting corrosion in gas wells includes a pyrazolopyridine derivative. The pyrazolopyridine derivative includes a pyridyl moiety, a first pyrazole moiety, a second pyrazole moiety, and a phenyl moiety. The first pyrazole moiety is bound to the pyridyl moiety. The second pyrazole moiety is bound to the pyridyl moiety. The phenyl moiety is bound to the pyridyl moiety. The composition can be flowed into a wellbore formed in a subterranean formation, thereby inhibiting corrosion in the wellbore.
Opening claim text (preview).
What is claimed is: 1. A method comprising: flowing a composition into a wellbore formed in a subterranean formation, thereby inhibiting corrosion in the wellbore, the composition comprising a pyrazolopyridine derivative comprising: a pyridyl moiety; a first pyrazole moiety bound to the pyridyl moiety, the first pyrazole moiety comprising an R 2 group selected from the group consisting of an alkyl group, a thiol group, a carboxyl group, an aromatic carbonyl group, a hydroxyl group, a methyl amino group, an amide group, and an ester group; a second pyrazole moiety bound to the pyridyl moiety, the second pyrazole moiety comprising an R 3 group selected from the group consisting of an alkyl group, an amide group, an amino group, a thiol group, a hydroxyl group, an ester group, and a carboxyl group; and a phenyl moiety bound to the pyridyl moiety; and producing a hydrocarbon from the subterranean formation via the wellbore. 2. The method of claim 1 , wherein the pyrazolopyridine derivative has a concentration in the composition in a range of from 100 parts per million (ppm) to 10,000 ppm. 3. The method of claim 2 , wherein the phenyl moiety further comprises an R 1 group selected from the group consisting of a methoxy group, a carboxyl group, an aromatic amide group, a thiol group, a nitrile group, an azo group, a pyridyl group, a bromophenyl group, and a sulfonic acid group. 4. The method of claim 3 , wherein the R 1 group is selected from the group consisting of methoxy, mercapto, pyridyl, (bromomethyl)pyridyl, and pyridine-2-aldoxime.
Compositions for in situ inhibition of corrosion in boreholes or wells · CPC title
Ortho-condensed systems · CPC title
containing a multiple nitrogen-to-carbon bond · CPC title
Heterocyclic compounds containing nitrogen as hetero atom · CPC title
Anticorrosion additives · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.