Methods and systems for suppressing corrosion of sensitive metal surfaces
US-10221347-B2 · Mar 5, 2019 · US
US12018210B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12018210-B2 |
| Application number | US-202218069091-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 20, 2022 |
| Priority date | May 11, 2018 |
| Publication date | Jun 25, 2024 |
| Grant date | Jun 25, 2024 |
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The invention includes methods for stimulating a hydrocarbon-bearing formation by perforating a wellbore and introducing an acidic composition in the wellbore. A preferred embodiment includes inserting an isolation plug in the wellbore at a predetermined location followed by inserting a perforating tool and a breakdown acid into the wellbore. The wellbore is perforated by the tool to create a perforated area. The breakdown acid is allowed to come into contact with the perforated area for a predetermined period of time sufficient to prepare the formation for stimulation. The tool is then removed from the wellbore wherein stimulation of the perforated area is thereby initiated. Also disclosed is a corrosion inhibiting composition for use with the acidic composition.
Opening claim text (preview).
The invention claimed is: 1. A method for the stimulation of a hydrocarbon-bearing formation, said method comprising steps of: providing a wellbore having a casing; inserting a plug in the wellbore at a location beyond a predetermined location; inserting a perforating tool, a wireline and a spearhead or breakdown acid composition into the wellbore; wherein said breakdown acidic composition is in direct contact with said perforating tool, said wireline and said casing; positioning the perforating tool at said predetermined location; perforating the wellbore with the perforating tool thereby creating a perforated area and acid soluble debris; causing the spearhead acid to come into contact with the perforated area for a predetermined period of time sufficient to prepare the hydrocarbon-bearing formation for frackling or stimulation; removing the perforating tool form the wellbore; initiating stimulation of the perforated area using a stimulation fluid: wherein the breakdown acidic composition comprises an acid and a corrosion inhibitor package and the breakdown acidic composition is balanced to complete an operation of dissolving the acid soluble debris and the balanced breakdown acidic composition will leave the perforating tool with less corrosion damage from exposure to the breakdown acidic composition; wherein said corrosion inhibitor package comprising comprises at least two compounds selected from: Group A; and Group F and where the at least two compounds are selected from different groups; and: wherein: Group A comprises compounds encompass within the following general chemical description: α, β-unsaturated aldehyde; Formaldehyde; Cinnamaldehyde; Group F comprises compounds encompassed within the following general chemical description: morpholine; aminoalkyl imidazolines; sarcosine; —two linked cyclic molecules with at least one nitrogen heterocycle, including quinoline+benzyl; imidazoline; and alkyl pyridine; step. 2. The method according to claim 1 where the Group A compound is selected from the group consisting of: α,β-unsaturated aldehyde selected from the group consisting of: cinnamaldehyde, t-cinnamaldehyde, crotonaldehyde, acrolein, methacrolein, leafaldehyde, citral, furfural, (E)-2-methyl-2-butenal, β-methyl-2-butenal, (E)-2-ethyl-2-butenal, (E)-2-ethyl-2-hexenal, 2-hexenal, 2-heptenal, 2-octenal, 2-nonenal, 2-decenal, 2-undecenal, 2-dodecenal, 2,4-hexadienal, 2,4-heptadienal, 2,4-octadienal, 2,4-nonadienal, 2,4-decadienal, 2,4-undecadienal, 2,4-dodecadienal, 2,6-dodecadienal, 1-formyl-[2-(2-methylvinyl)]-2-n-octylethylene, dicinnamaldehyde, p-hydroxycinnamaldehyde, p-methylcinnamaldehyde, pethylcinnamaldehyde, p-methoxycinnamaldehyde, pdimethylaminocinnamaldehyde, p-diethylaminocinnamaldehyde, pnitrocinnamaldehyde, o-nitrocinnamaldehyde, o-allyloxycinnamaldehyde, 4-(3-propenal)cinnamaldehyde, p-sodiumsulfocinnamaldehyde, ptrimethylammoniumcinnamaldehydesulfate, ptrimethylammoniumcinnamaldehydeo-methylsulfate, pthiocyanocinnamaldehyde, p-(S-acetyl)thiocinnamaldehyde, p-(S—N,Ndimethylcarbamoylthio) cinnamaldehyde, p-chlorocinnamaldehyde, 5-phenyl-2,4-pentadienal, 5-(p-methoxyphenyl)-2,4-pentadienal, 2,3-diphenylacrolein, 3,3-diphenylacrolein, α-methylcinnamaldehyde, β-methylcinnamaldehyde, α-chlorocinnamaldehyde, α-bromocinnamaldehyde, α-butylcinnamaldehyde, α-amylcinnamaldehyde, α-hexylcinnamaldehyde, 2-(p-methylbenzylidine)decanal, α-bromo-p-cyanocinnamaldehyde, α-ethyl-p-methylcinnamaldehyde, p-methyl-α-pentylcinnamaldehyde, 3,4-dimethoxy-α-methylcinnamaldehyde, α-[(4-methylphenyl)methylene]benzeneacetaldehyde, α-(hydroxymethylene)-4-methylbenzylacetaldehyde, 4-chloro-α-(hydroxymethylene)benzeneacetaldehyde, α-nonylidenebenzeneacetaldehyde, derivatives thereof, and combinations thereof. 3. The method according to claim 1 where the corrosion inhibition package can be selected from the following combinations of group where reactions occur between compounds of said groups: a compound of Group F reacted with a compound of Group A.
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