Corrosion inhibition of HCL treatment fluids with environmentally compatible solvent

Patent metadata

Field	Value
Publication number	US-11066749-B2
Application number	US-202016780488-A
Country	US
Kind code	B2
Filing date	Feb 3, 2020
Priority date	May 27, 2015
Publication date	Jul 20, 2021
Grant date	Jul 20, 2021

Abstract

A method of treating in a subterranean formation including placing a corrosion inhibitor composition into a subterranean formation, where the formation includes an acidic environment having a pH of about 5 or below, where the composition includes: an organic solvent comprising an alcohol with a flash point of at least about 75° C.; a nitrogen containing compound; an aqueous acid solution comprising HCl; and contacting a metal surface with the corrosion inhibitor composition. A corrosion inhibitor composition includes an organic solvent comprising an alcohol with a flash point of at least about 75° C.; a nitrogen containing compound; and an aqueous acid solution comprising HCl.

First claim

What is claimed is:

1. A corrosion inhibitor composition comprising:
an organic solvent comprising tetrahydrofurfuryl alcohol;
a nitrogen containing compound, wherein the nitrogen containing compound includes at least one of:
the product of a reaction between at least one aldehyde and at least one amide that is not formamide or a formamide derivative;
a quaternary nitrogen containing compound; and
combinations thereof, and

an aqueous acid solution comprising HCl.

2. The composition of claim 1 , wherein the organic solvent is present in an amount of about 5% to about 100% by weight of the aqueous acid solution.

3. The composition of claim 1 , wherein the at least one aldehyde comprises at least one aldehyde selected from the group consisting of 2-hydroxynapthaldehyde, 7-phenyl-2,4,6-heptatrienal, crotonaldehyde, 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, citral, 1-formyl-[2-(2 methylvinyl)]-2-n-octylethylene, cinnamaldehyde, dicinnamaldehyde, p-hydroxycinnamaldehyde, p-methylcinnamaldehyde, p-ethylcinnamaldehyde, p-methoxycinnamaldehyde, p-dimethylaminocinnamaldehyde, p-diethylaminocinnamaldehyde, p-nitrocinnamaldehyde, o-nitrocinnamaldehyde, o-allyloxycinnamaldehyde, 4-(3-propenal)cinnamaldehyde, p-sodium sulfocinnamaldehyde, p-trimethylammoniumcinnamaldehyde sulfate, p-trimethylammoniumcinnamaldehyde o-methylsulfate, p-thiocyanocinnamaldehyde, p-(S-acetyl)thiocinnamaldehyde, p-(S—N,N dimethylcarbamoylthio)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, 3,7-dimethyl-2,6-octadienal, cinnamaloxime, cinnamonitrile, and beta-hydroxy aldehydes which dehydrate to form alpha,beta-unsaturated aldehydes under acidic conditions, glyoxylic acid, glyoxal, and combinations thereof.

4. The composition of claim 1 , wherein the at least one amide comprises at least one amide selected from the group consisting of acetamide, N-methylacetamide, trichloroacetamide, N-methyltrichloroacetamide, propanamide, N-methylpropanamide, butanamide, N-methylbutanamide, pentanamide, N-methylpentanamide, hexanamide, N-methylhexanamide, benzamide, N-methylbenzamide, 1-naphthylamide, N-methyl-1-naphthylamide, 2-naphthylamide, N-methyl-2-naphthylamide, o-toluamide, N-methyl-o-toluamide, m-toluamide, N-methyl-m-toluamide, p-toluamide, N-methyl-ptoluamide, thiobenzamide, 4-pyridinethioamide, ethionamide, pyrazine-2-thiocarboxamide, nicotinamide, stearamide, 2,2-diethoxyacetamide and lauric acid amide, amides derived from primary or secondary amines, and combinations thereof.

5. The composition of claim 4 , wherein said primary or secondary amine is selected from the group consisting of ethanolamine, diethanolamine, partially ethoxylated dehydroabietylamine, ethylamine, diethylamine, dehydroabietylamine, propylamine, dipropylamine, propanolamine, isopropanolamine, 2-propanol-1-amine, diisopropanolamine, butylamine, dibutylamine, tert-butylamine, pentylamine, dipentylamine, tert-benzyl-tert-butylamine, 3,4-diaminofuran, 2,4-diamino-6-phenyl-1,3,5-triazine, 2,4-diamino-6-methyl-1,3,5-triazine, 2,4 diamino-6,-hydroxy-1,3, 5-triazine, 2,4-diamino-6-chloro-1,3,5-triazine, 2,5-diaminotoluene, 2,6-diamino pyridine, 2,6 diaminotoluene, 2,4-diaminotoluene, m-phenylenediamine, p-phenylenediamine, 4-methyl-m-phenylenediamine, 2,5 diaminotoluene sulfate, 2-methyl-1,3-benzenediamine, 5-chloro-1,3-phenylenediamine, 2,4,6-trimethyl-1,3-benzenediamine, 3,5-diaminobenzoic acid, 3-nitro-1,2-benzenediamine, 2-nitro-1,2-benzenediamine, 1,3-benzenediamine, 4-nitro-1,2-benzenediamine, 3-nitro-1,3-phenylenediamine, 2′,4′-diaminoacetanilide, N-(3-aminophenyl)butanamide, 2,4-diaminobenZenesulfonic acid, 4-ethoxy-1,3-phenylenediamine 2HCl, 2,4-bis(butylamino)-3-oxo-1-cyclobutenylium-1-olate, 2,4-bis(3-benzamidopropylamino) 3-oxo-1-cyclobutenylium-1-olate, 4-imino-5-methyl-2 nitramino-4H-imidazole, 2,5-diacetamido-1,3,4-thiadiazole, 5-amino-1,3,3-trimethylcyclohexanemethylamine and combinations thereof.

6. The composition of claim 1 , wherein the quaternary nitrogen containing compound comprises quaternized amino or amide containing compounds of molecular weight less than 1500 g/mol.

7. The composition of claim 1 , wherein the product of the reaction between at least one aldehyde and at least one amide comprises a compound with at least one the following structures:

where R is H, methyl, ethyl, hydroxy, methoxy, ethoxy, bromo, chloro, fluoro, mercapto, dimethylamino, diethylamino groups, N-alkyl, N-cycloalkyl and N-alkylarylpyridinium halides, N-cyclohexylpyridinium bromide or chloride, N-alkyl, N-cycloalkyl, N-alkylarylquinolinium halides, N-dodecylquinolinium bromide or chloride, and combinations thereof.

8. The composition of claim 1 , wherein the aqueous acid solution further comprises at least one of formic acid, acetic acid, citric acid, glycolic acid, hydroxyacetic acid, lactic acid, maleic acid, hydrofluoric acid, 3-hydroxypropionic acid, carbonic acid, glutamic acid N,N-diacetic acid or a salt thereof (GLDA), hydroxyimino disuccinic acid (HIDS) and/or methylglycine N,N-diacetic acid or a salt thereof (MGDA), β-alanine diacetic acid, ethylenediaminedisuccinic acid, iminodisuccinic acid, N-tris[(1,2-dicarboxyethoxy)ethyl]amine, N-bis[2-(carboxymethoxy)ethyl]glycine, N-bis[2-(1,2-dicarboxyethoxy)ethyl]glycine, N-bis[2-(1,2-dicarboxyethoxy)ethyl]aspartic acid, N-bis[2-(methylcarboxymethoxy)ethyl]glycine, N-bis[2-(1,2-dicarboxyethoxy)ethyl]methylglycine, any salt thereof, any derivative thereof, and any combination thereof.

9. The composition of claim 1 , further comprising at least one of potassium iodide, sodium iodide, and combinations thereof.

10. The composition of claim 1 , further comprising at least one of ethylene glycol, diethylene glycol, propylene glycol, surfactants, and combinations thereof.

11. The composition of claim 10 , wherein the surfactants are selected from the group consisting of linear alcohol ethoxylates, amine alcohol ethoxylates, ethoxylated amides, ethoxylated alkyl amines, alkylphenol, alkyoxylated fatty acids, and combinations thereof.

Assignees

• Halliburton Energy Services Inc

Inventors

• Reyes Enrique Antonio
• Lablanc Alyssa Lynn
• Beuterbaugh Aaron M

Classifications

• C09K2208/32

  Anticorrosion additives · CPC title

• C09K5/10

  Liquid materials · CPC title

• C23F11/04 Primary

  in markedly acid liquids · CPC title

• C09K8/74

  combined with additives added for specific purposes · CPC title

• C09K8/54

  Compositions for in situ inhibition of corrosion in boreholes or wells · CPC title