Single-phase retarded acid systems using amino acids
US-2024360356-A1 · Oct 31, 2024 · US
US2016145487A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016145487-A1 |
| Application number | US-201314898336-A |
| Country | US |
| Kind code | A1 |
| Filing date | Sep 11, 2013 |
| Priority date | Sep 11, 2013 |
| Publication date | May 26, 2016 |
| Grant date | — |
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The present invention relates to an asphaltene-dissolving oil-external emulsion for acidization and methods of using the same. In various embodiments, the present invention provides a method of treating a subterranean formation, including obtaining or providing an oil-external water-internal emulsion. The emulsion includes an asphaltene-dissolving composition, emulsifier, and aqueous acid. The method also includes placing the composition in a subterranean formation downhole.
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1 - 119 . (canceled) 120 . A method of treating a subterranean formation, the method comprising: placing in the subterranean formation a composition comprising an oil-external water-internal emulsion comprising an asphaltene-dissolving composition; emulsifier; and aqueous acid. 121 . The method of claim 120 , wherein the composition is substantially free of diesel. 122 . The method of claim 120 , wherein the composition is substantially free of organophilic clay. 123 . The method of claim 120 , wherein the composition is substantially free of lignite. 124 . The method of claim 120 , wherein the composition is substantially free of benzene, toluene, ethylbenzene, and xylenes. 125 . The method of claim 120 , wherein the external phase comprises the asphaltene-dissolving composition. 126 . The method of claim 120 , wherein the asphaltene-dissolving composition comprises an aromatic hydrocarbon composition. 127 . The method of claim 126 , wherein the aromatic hydrocarbon composition comprises aromatic petroleum naphtha. 128 . The method of claim 126 , wherein the aromatic hydrocarbon composition comprises a mono or poly(C 0 -C 10 )alkyl-substituted (C 5 -C 30 )aromatic hydrocarbon ring system, wherein each alkyl is independently substituted or unsubstituted, wherein each aromatic ring is independently substituted or unsubstituted. 129 . The method of claim 126 , wherein the aromatic hydrocarbon composition comprises a C 10 -C 22 compound that is a fused aromatic hydrocarbon ring system. 130 . The method of claim 126 , wherein the aromatic hydrocarbon composition comprises at least one of a di(C 1 -C 5 )alkylbenzene and a tri(C 1 -C 5 )alkylbenzene. 131 . The method of claim 126 , wherein the aromatic hydrocarbon composition comprises a di(C 1 -C 5 )alkylbenzene. 132 . The method of claim 126 , wherein the aromatic hydrocarbon composition comprises a (C 1 -C 5 )alkylbenzene. 133 . The method of claim 126 , wherein the asphaltene-dissolving composition comprises a polar organic solvent miscible with the aromatic hydrocarbon composition. 134 . The method of claim 120 , wherein the asphaltene-dissolving composition comprises a polar organic solvent. 135 . The method of claim 120 , wherein the internal phase of the oil-external emulsion comprises the aqueous acid, wherein the acid is at least one of hydrochloric acid, sulfuric acid, fluoric acid, nitric acid, phosphoric acid, boric acid, hydrobromic acid, perchloric acid, acetic acid, formic acid, lactic acid, citric acid, oxalic acid, uric acid, glutaric acid, glutamic acid, adipic acid, and phthalic acid. 136 . The method of claim 120 , wherein the emulsifier comprises at least one of a sulfate, sulfonate, phosphate, carboxylate, tri(C 1 -C 10 )alkylammonium halide, substituted or unsubstituted fatty alcohol, substituted or unsubstituted fatty acid, substituted or unsubstituted fatty acid ester, and a substituted or unsubstituted poly((C 1 -C 10 )hydrocarbylene oxide) independently having H or (C 1 -C 10 )hydrocarbylene as end-groups. 137 . The method of claim 120 , wherein the emulsifier comprises ammonium aluryl sulfate, sodium lauryl sulfate, sodium laureth sulfate, sodium myreth sulfate, dioctyl sodium sulfosuccinate, perfluorooctanesulfonate, perfluorobutanesulfonate, linear (C 1 -C 10 )alkylbenzene sulfonate, sodium stearate, sodium lauroyl sarcosinate, perfluorononanoate, perfluorooctanoate, octenidine dihydrochloride, certyl trimethylammonium bromide, cetyl trimethylammonium chloride, cetylpyridinium chloride, benzalkonium chloride, benzethonium chloride, 5-bromo-5-nitro-1,3-dioxane, dimethyldiactadecylammonium chloride, cetrimonium bromide, dioctadecyldimethylammonium bromide, 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate, cocamidopropyl hydroxysultaine, cocamidopropyl betaine, lecithin, a polyoxyethylene glycol alkyl ether, a polyoxypropylene glycol ether, a glucoside alkyl ether, a polyoxyethylene glycol octylphenol ether, a polyoxyethylene glycol alkylphenol ether, a glycerol alkyl ether, a polyoxyethylene glycol sorbitan alkyl ester, cocamide monoethanolamine, cocamide diethanolamine, dodecyldimethylaminde oxide, a poloxamer, and a polyethoxylated tallow amine. 138 . A method of treating a subterranean formation, the method comprising: placing in the subterranean formation a composition comprising an oil-external water-internal emulsion comprising an external phase comprising an asphaltene-dissolving composition comprising heavy aromatic petroleum naphtha and a polar organic compound miscible with the heavy aromatic petroleum naptha, wherein the external phase is about 10% to about 50% of the oil-external emulsion by volume; an internal phase comprising aqueous acid, wherein the internal phase is about about 50% to about 90% of the oil-external emulsion by volume; and emulsifier comprising a polyaminated fatty acid. 139 . A system comprising: a tubular disposed in a subterranean formation; and a pump configured to pump a composition comprising an oil-external water-internal emulsion through the tubular in the subterranean formation, the oil-external water-internal emulsion comprising an asphaltene-dissolving composition; emulsifier; and aqueous acid.
Enhanced recovery methods for obtaining hydrocarbons · CPC title
combined with additives added for specific purposes · CPC title
Anticorrosion additives · CPC title
Oil-based compositions · CPC title
organic depositions, e.g. paraffins or asphaltenes · CPC title
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