US2659693A - Process for preventing corrosion of ferrous metals - Google Patents

Process for preventing corrosion of ferrous metals Download PDF

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US2659693A
US2659693A US287243A US28724352A US2659693A US 2659693 A US2659693 A US 2659693A US 287243 A US287243 A US 287243A US 28724352 A US28724352 A US 28724352A US 2659693 A US2659693 A US 2659693A
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corrosion
double
quaternary ammonium
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Melba L Lytle
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Standard Oil Development Co
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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • C23F11/14Nitrogen-containing compounds
    • C23F11/141Amines; Quaternary ammonium compounds
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S507/00Earth boring, well treating, and oil field chemistry
    • Y10S507/939Corrosion inhibitor

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  • the present invention relates to the inhibition of corrosion of corrodible ferrous metal surfaces by corrosive fluids. More particularly, the invention relates to a process for inhibiting the corrosivity of fiuids produced from subsurface earth formations exposed to corrodible ferrous metal conduits and attendant equipment through which the fluids are flowed and processed.
  • brines may contain corrosive sulfides which may include alkali metal sulfides, alkaline earth metal sulfides, acid sulfides, such as hydrogen sulfides, and/or organic sulfides.
  • the well fluids, such as crude oil and gas, and the brines associated therewith may also contain'carbon dioxide, a weal; inorganic acid, organic acids and the like.
  • the brines containing hydrogen sulfide or carbon dioxide and organic acids are especially corrosive to iron and steel equipment. Since the corrosive materials occur in or are introduced into the fluids originating in the subsurface formations, corrosion may occur throughout the ferrous metal conduits and attendant equipment through which the fluids from the subsurface formations are flowed and produced. In some cases, the corrosion may be more or less localized to a limited portion of the conduits from which fluids from the subsurface formations are produced. In any case, the corrosion of the conduits and attendant ferrous metal equipment may be so severe as to require replacement of either or of both. As is well recognized, such replacements can be and often are extremely expensive. The expense is not limited merely to the cost of replacing the corroded equipment but may also involve killing pens.
  • the present invention may be described briefly v as involving the prevention of corrosion of ferrous metals exposed to a corrosive solution in which there is incorporated in the corrosive solu- 2 tion an effective amount of a double, long-chain quaternary ammonium salt represented by the formula:
  • R is a radical having an alkyl chain containing at least 8 carbon atoms or a radical having at least 8 carbon atoms and a henzyl group
  • R1 is an alkyl radical having no more than 2 carbon atoms or a radical containing a benzyl group
  • A is a normal hydrocarbon chain having from 4 to 16 methylene groups, an aryl radical, or an alkyl substituted aryl radical, while X is a halogen such as chlorine, bromine, or iodine.
  • the invention also has to do with the prevention of corrosion in oil and gas well equipment by incorporating in the Well an effective amount of a double, long-chain quaternary ammonium salt as represented by the foregoing structural formula.
  • the double, long-chain quaternary ammonium salt as has been described, is injected into the well, it suitably may be iniected into the annulus and displaced upwardly into the tubing or oil string.
  • the double, longchain quaternary ammonium salt employed in the present invention may be used to coat the tubing string before it is arranged in the well and thereby obtain quickly the desired protection.
  • One method of in ecting the double, long-chain quaternary ammonium salt employed in the present invention is to dissolve it in a suitable solvent, such as water, or an aromatic hydrocarbon solvent, such as re resented by benzene, toluene, xylene and the higher members of the same homologous series.
  • a suitable solvent such as water, or an aromatic hydrocarbon solvent, such as re resented by benzene, toluene, xylene and the higher members of the same homologous series.
  • the double, long-chain quaternary ammonium salt may be introduced into the annulus of the well between the casing and the producing string,
  • the inner wall 01' the casing and the outer and inner walls of the tubing string and the inner surfaces oi. the auxiliary equipment, such as wellhead equipment, fiow lines and thelike, are contacted with the double, long chain quaternary ammonium salt and protected from corrosion from the corrosive materials in the well fluid.
  • the amount of the double, long-chain quaternary ammonium salt to be employed depends on the corrosivity oi the corrosive solution.
  • the amount of the double, long-chain quaternary ammonium salt necessary to protect adequately the ferrous metal surfaces to which it is applied will be only a small concentration in the corrosive fluid. For example, an amount from about .0001% to about 005% by weight will give effective protection in substantially all corrosive fluids produced from subsurface formations.
  • the double, long-chain quaternary ammonium salts employed in the practice of the present invention are exemplified by those double, longchain quaternary ammonium salts as represented by the foregoing structural formula.
  • Specific examples of such compounds are decamethylene bis(dimethyl cetyl ammonium bromide), tetramethylene bis(dimethyl cetyl ammonium bro mide), butene bis(nonyl benzyl dimethyl ammonium chloride), butyne bis(2 octyl benzyl dimethyl ammonium chloride) and butane bis(nonyl) benzyl dimethyl ammoniumchloride.
  • Other compounds of a similar nature which may be employed in the practice of the present invention are described in U.
  • tetramethylene bis(dimethyl cetyl ammonium bromide) In order to test the efiectiveness of tetramethylene bis(dimethyl cetyl ammonium bromide) a fifty-fifty mixture of West Texas crude oil and West Texas brine was saturated with hydrogen sulfide and divided into three portions. To one portion 0.003% by weight of tetramethylene bis(dimethyl cetyl ammonium bromide) was added and to another portion 0.001% by weight of the tetramethylene bis(dimethyl cetyl ammonium bromide) was added. The third portion of the mixture of West Texas crude oil and West Texas brine saturated with hydrogen sulfide without addition of tetramethylene bis(dimethyl cetyl ammonium bromide) was used as a control.
  • Mild carbon steel coupons were immersed 31 times a minute for a period of 14 days in each of the 3 portions of the mixture saturated with hydrogen sulfide. After the period indicated, it was found that the coupons in the corrosive solution which contained no tetramethylene bis(dimethyl cetyl ammonium bromide) had been corroded at a rate of 0.025 inch per year.
  • the corrosion rate of the solution of crude oil and brine saturated with hydrogen sulfide was reduced 92% by 0.003% by weight of the tetramethylene bis(dimethyl cetyl ammonium bromide) and was reduced 22% 4 by 0.001% by weight of the tetramethylene bis(dimethyl cetyl ammonium bromide).
  • Decamethylene bis(dimethyl cetyl ammonium bromide) was tested in a similar mixture of West Texas crude oil and West Texas brine saturated with hydrogen sulfide in three concentrations as follows: 0.003% by weight, 0.001% by weight, and 0.0005% by weight. After the carbon steel ecupons had been immersed 31 times per minute for a period of 14 days in the corrosive solution, it was found that when compared with the control coupons, 0.003% by weight of decamethylene bis(dimethyl cetyl ammonium bromide) had e1- fected 99% reduction in corrosivity, 0.001% by weight of the decamethylene bis(dimethyl cetyl ammonium bromide) had effected a reduction in corrosivity. of 75%, and 0.0005% by weight of decamethylene bis(dimethyl cetyl ammonium bromide) had effected a reduction in corrosion rate of 27%.
  • dimethyl benzyl lauryl ammonium chloride cetyl trimethyl ammonium bromide, and stearyl dimethyl benzyl ammonium chloride were compared with butene bis(nonyl benzyl dimethyl ammonium chloride), butyne bis(2 octyl benzyl dimethyl ammonium chloride), and butane bis(nonyl benzyl dimethyl ammonium chloride).
  • Ortho-xylylene bislcetyl dimethyl ammonium bromide was added in an amount of 0.002 weight per cent to a fifty-fifty mixture of West Texas crude oil and West Texas brine which had been saturated with hydrogen sulfide.
  • the hydrogen sulfide-saturated mixture then had mild carbon steel coupons immersed in it thirty-one times a minute for a period of fourteen days. After the period indicated, it was found that the coupons in the corrosive solution which contained orthoxylylene bis(cetyl dimethyl ammonium bromide) had been corroded at an average rate of 0.00075 inch per year.
  • Metal coupons were also immersed in the corrosive solution to which ortho-xylylene bisicetyl dimethyl ammonium bromide) had not been added. After a similar treatment of immersions over the same period of time it was found that the metal coupons in the corrosive solution to which no inhibitor had been added had been corroded to an extent of 0.0261 inch per year. Thus, the orthoxylylene bis(cetyl dimethyl ammonium bromide) reduced the corrosion rate of the corrosive solution by 97%.
  • a process for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises incorporating in said corrosive solution an effective amount of a double, longchain quaternary ammonium salt represented by the formula:
  • R is a radical selected from the group consisting of the radicals having an alkyl chain containing at least 8 carbon atoms and an alkyl chain having at least 8 carbon atoms and a benzyl group
  • R1 is selected from the group consisting of the alkyl radicals having no more than 2 carbon atoms and the benzyl group radicals
  • A is selected from the group consisting of normal hydrocarbon chains having from 4 to 16 methylens groups, aryl radicals, and alkyl substituted aryl radicals
  • X is a halogen selected from the group consisting of chlorine, bromine, and iodine.
  • a process for preventing the corrosion of ferrous metals exposed to a corrosive solution including a hydrocarbon and water which comprises incorporating in said corrosive solution an effective amount of a double, long-chain quaternary ammonium salt represented by the formula:
  • R is a radical selected from the group consisting of the radicals having an alkyl chain containing at least 8 carbon atoms and an alkyl chain having at least 8 carbon atoms and a benzyl group
  • R1 is selected from the group consisting of the alkyl radicals having no more than 2 carbon atoms and the benzyl group radicals
  • A is selected from the group consisting of normal hydrocarbon chains having from 4 to 16 methylene groups, aryl radicals, and alkyl substituted aryl radicals
  • X is a halogen selected from the group consisting of chlorine, bromine, and iodine.
  • a method for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises incorporating in said corrosive solution an effective amount of decamethylene bis dimethyl cetyl ammonium bromide).
  • a process for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises incorporating in said corrosive solution an effective amount of tetramethylene bis(dimethyl cetyl ammonium bromide).
  • a process for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises incorporating in said corrosive solution an effective amount of butene bisfnonyl benzyl dimethyl ammonium chloride).
  • a process for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises incorporating in said corrosive solution an effective amount of butyne bis12 octyl benzyl diinethyl ammonium chloride).
  • a process for preventing the corrosion of ferrous metals which comprises incorporating in said corrosive solution an effective amount of butane bis(nonyl benzyl dimethyl ammonium chloride).
  • a process for preventing corrosion in oil and gas Well equipment which comprises the step of injecting into the well an effective amount of a double, long-chain quaternary ammonium salt represented by the formula:
  • R is a radical selected from the group consisting of the radicals having an alkyl chain containing at least 8 carbon atoms and an alkyl chain having at least 8 carbon atoms and a benzyl group
  • R1 is selected from the group consisting of the alkyl radicals having no more than 2 carbon atoms and the benzyl group radicals
  • A is selected from the group consisting of normal hydrocarbon chains having from 4 to 16 methylene groups, aryl radicals and alkyl substituted aryl radicals
  • X is a halogen selected from the group consisting of chlorine, bromine, and iodine.
  • a process for preventing the corrosion of oil and gas well equipment which comprises incorporating into a well fluid an effective amount of a double, long-chain quaternary ammonium salt represented by the formula:
  • R is a radical selected from the group consisting of the radicals having an alkyl chain containing at least 8 carbon atoms and an alkyl chain having at least 8 carbon atoms and a benzyl group
  • R1 is selected from the group consisting of the alkyl radicals having no more than 2 carbon atoms and the benzyl group radicals
  • A is selected from the group consisting of normal hydrocarbon chains having from 4 to 16 methylene groups, aryl radicals, and alkyl sub stituted aryl radicals
  • X is a halogen selected from the group consisting of chlorine. bromine, and iodine.
  • a method for preventing corrosion of oil and gas well equipment which comprises injecting into the well an effective amount of decamethylene bisl'dimethyl cetyl ammonium bromide).
  • a method for preventing corrosion of oil and gas well equipment which comprises injecting into the well an effective amount of tetra methylene bisidimethyl cetyl ammonium bromide).
  • a method for preventing corrosion of oil and gas well equipment which comprises inject ing into the well an eflective amount of butene bisinonyl bcnzyl dimethyl ammonium chloride).
  • a method for preventing corrosion of oil and gas well equipment which comprises injecting into the well an effective amount of butyne bis(2 octyl bcnzyl dimethyl ammonium chloride).
  • a method for preventing corrosion of oil and gas well equipment which comprises injecting into the well an effective amount of butane bismonyl benzyl dimethyl ammonium chloride).
  • a process for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises applying to said metals a double, longchain quaternary ammonium salt rep resented by the formula:
  • R is a radical selected from the group consisting of the radicals having an alkyl chain containing at least 8 carbon atoms and an alkyl chain having at least 8 carbon atoms and a benzyl group
  • R1 is selected from the group consisting of the alkyl radicals having no more than 2 carbon atoms and the benzyl group radicals
  • A is selected from the group consisting of normal hydrocarbon chains having from 4 to 15 methylene groups, aryl radicals and alkyl substituted aryl radicals
  • X i a halogen selected from the group consisting of chlorine, bromine, and iodine.

Description

Patented Nov. 17, 1953 PROCESS FOR PREVENTING CORROSION OF FERROUS METALS Melba L. Lytle, Houston, Tex., assignor, by mesne assignments, to Standard Oil Development Company, Elizabeth, N. J.,' a corporation of Delaware No Drawing. Application May 10, 1952, Serial No. 287,243
20 Claims. 1
The present invention relates to the inhibition of corrosion of corrodible ferrous metal surfaces by corrosive fluids. More particularly, the invention relates to a process for inhibiting the corrosivity of fiuids produced from subsurface earth formations exposed to corrodible ferrous metal conduits and attendant equipment through which the fluids are flowed and processed.
In the production of oil and gas, soluble sulfides are often produced from subsurface formations and in the presence of water will attack or corrode ferrous metal conduits and attendant equipment with which the crude oil or gas comes into contact. In the production of such oil and gas there is usually produced brine along with the sour crude or sour gas. These brines may contain corrosive sulfides which may include alkali metal sulfides, alkaline earth metal sulfides, acid sulfides, such as hydrogen sulfides, and/or organic sulfides. The well fluids, such as crude oil and gas, and the brines associated therewith may also contain'carbon dioxide, a weal; inorganic acid, organic acids and the like. The brines containing hydrogen sulfide or carbon dioxide and organic acids are especially corrosive to iron and steel equipment. Since the corrosive materials occur in or are introduced into the fluids originating in the subsurface formations, corrosion may occur throughout the ferrous metal conduits and attendant equipment through which the fluids from the subsurface formations are flowed and produced. In some cases, the corrosion may be more or less localized to a limited portion of the conduits from which fluids from the subsurface formations are produced. In any case, the corrosion of the conduits and attendant ferrous metal equipment may be so severe as to require replacement of either or of both. As is well recognized, such replacements can be and often are extremely expensive. The expense is not limited merely to the cost of replacing the corroded equipment but may also involve killing pens.
The present invention may be described briefly v as involving the prevention of corrosion of ferrous metals exposed to a corrosive solution in which there is incorporated in the corrosive solu- 2 tion an effective amount of a double, long-chain quaternary ammonium salt represented by the formula:
In the formula R is a radical having an alkyl chain containing at least 8 carbon atoms or a radical having at least 8 carbon atoms and a henzyl group; R1 is an alkyl radical having no more than 2 carbon atoms or a radical containing a benzyl group; A is a normal hydrocarbon chain having from 4 to 16 methylene groups, an aryl radical, or an alkyl substituted aryl radical, while X is a halogen such as chlorine, bromine, or iodine.
The invention also has to do with the prevention of corrosion in oil and gas well equipment by incorporating in the Well an effective amount of a double, long-chain quaternary ammonium salt as represented by the foregoing structural formula.
When the double, long-chain quaternary ammonium salt, as has been described, is injected into the well, it suitably may be iniected into the annulus and displaced upwardly into the tubing or oil string. If desired, the double, longchain quaternary ammonium salt employed in the present invention may be used to coat the tubing string before it is arranged in the well and thereby obtain quickly the desired protection.
One method of in ecting the double, long-chain quaternary ammonium salt employed in the present invention is to dissolve it in a suitable solvent, such as water, or an aromatic hydrocarbon solvent, such as re resented by benzene, toluene, xylene and the higher members of the same homologous series.
It may be desired to iniect the corros on inhibitor, in accordance with my invention, either continuously or' intermittently. Continuous application is the preferred method.
In the practice of the present invention for the protection of metal equipment of oil and gas wells such as those producing well fluids containing an acidic constituent, such as hydrogen sulfide, carbon dioxide, or anic acids and other corrosive materials as has been mentioned, the double, long-chain quaternary ammonium salt may be introduced into the annulus of the well between the casing and the producing string,
where it becomes intimately admixed with the well fluid and may be pumped or flowed from the well with the corrosive fluids. Thus, the inner wall 01' the casing and the outer and inner walls of the tubing string and the inner surfaces oi. the auxiliary equipment, such as wellhead equipment, fiow lines and thelike, are contacted with the double, long chain quaternary ammonium salt and protected from corrosion from the corrosive materials in the well fluid.
It may be desirable to introduce the double, long-chain quaternary ammonium salt, the identity of which has been given, into the annulus by means of a mechanical pump so that a small amount ofthe m aterial in a suitable solvent, as has been specified, is introduced continuously or intermittently, as is desired.
The amount of the double, long-chain quaternary ammonium salt to be employed depends on the corrosivity oi the corrosive solution. The amount of the double, long-chain quaternary ammonium salt necessary to protect adequately the ferrous metal surfaces to which it is applied will be only a small concentration in the corrosive fluid. For example, an amount from about .0001% to about 005% by weight will give effective protection in substantially all corrosive fluids produced from subsurface formations.
The double, long-chain quaternary ammonium salts employed in the practice of the present invention are exemplified by those double, longchain quaternary ammonium salts as represented by the foregoing structural formula. Specific examples of such compounds are decamethylene bis(dimethyl cetyl ammonium bromide), tetramethylene bis(dimethyl cetyl ammonium bro mide), butene bis(nonyl benzyl dimethyl ammonium chloride), butyne bis(2 octyl benzyl dimethyl ammonium chloride) and butane bis(nonyl) benzyl dimethyl ammoniumchloride. Other compounds of a similar nature which may be employed in the practice of the present invention are described in U. S, Patents 2,525,777, 2,525,778 and 2,525,779, issued October 17, 1950, to de Bonneville and Gormly. The double, longchain quaternary ammonium salts described by de Bonneville et al. are also excellent inhibitors for corrosion for use in my invention.
In order to illustrate the beneficial results obtained in the practice of the present invention the following examples are given:
In order to test the efiectiveness of tetramethylene bis(dimethyl cetyl ammonium bromide) a fifty-fifty mixture of West Texas crude oil and West Texas brine was saturated with hydrogen sulfide and divided into three portions. To one portion 0.003% by weight of tetramethylene bis(dimethyl cetyl ammonium bromide) was added and to another portion 0.001% by weight of the tetramethylene bis(dimethyl cetyl ammonium bromide) was added. The third portion of the mixture of West Texas crude oil and West Texas brine saturated with hydrogen sulfide without addition of tetramethylene bis(dimethyl cetyl ammonium bromide) was used as a control. Mild carbon steel coupons were immersed 31 times a minute for a period of 14 days in each of the 3 portions of the mixture saturated with hydrogen sulfide. After the period indicated, it was found that the coupons in the corrosive solution which contained no tetramethylene bis(dimethyl cetyl ammonium bromide) had been corroded at a rate of 0.025 inch per year. The corrosion rate of the solution of crude oil and brine saturated with hydrogen sulfide was reduced 92% by 0.003% by weight of the tetramethylene bis(dimethyl cetyl ammonium bromide) and was reduced 22% 4 by 0.001% by weight of the tetramethylene bis(dimethyl cetyl ammonium bromide).
Decamethylene bis(dimethyl cetyl ammonium bromide) was tested in a similar mixture of West Texas crude oil and West Texas brine saturated with hydrogen sulfide in three concentrations as follows: 0.003% by weight, 0.001% by weight, and 0.0005% by weight. After the carbon steel ecupons had been immersed 31 times per minute for a period of 14 days in the corrosive solution, it was found that when compared with the control coupons, 0.003% by weight of decamethylene bis(dimethyl cetyl ammonium bromide) had e1- fected 99% reduction in corrosivity, 0.001% by weight of the decamethylene bis(dimethyl cetyl ammonium bromide) had effected a reduction in corrosivity. of 75%, and 0.0005% by weight of decamethylene bis(dimethyl cetyl ammonium bromide) had effected a reduction in corrosion rate of 27%.
Since it has been known to use quaternary ammonium compounds other than the double, longchain quaternary ammonium salts as corrosion inhibitors, a comparison was made between the conventional quaternary ammonium salts and the double, long-chain quaternary ammonium salts employed in accordance with the present invention. Thus, varying amounts of dimethyl benzyl lauryl ammonium chloride, cetyl trimethyl ammonium bromide, and stearyl dimethyl benzyl ammonium chloride were compared with butene bis(nonyl benzyl dimethyl ammonium chloride), butyne bis(2 octyl benzyl dimethyl ammonium chloride), and butane bis(nonyl benzyl dimethyl ammonium chloride). In these comparative tests varying amounts oil the several inhibitors of the prior art and the corrosion inhibitors employed in the present invention were added to a mixture of fifty-fifty West Texas crude oil and West Texas brine which had been saturated with hydrogen sulfide and mild carbon steel coupons were immersed 31 times a minute in the corrosive solution of crude oil and brine containing hydrogen sulfide for a period of 14 days and at the end of the period the coupons were removed and compared to determine the corrosion rate by reduction in per cent. In short, metal coupons were immersed in the corrosive solution in the absence of any inhibitor and the percentage reduction eifected by the several inhibitors was determined by comparison with the blanks. The data obtained in the following table illustrate the effectiveness of the several inhibitors:
Table gg zggi Corrosion Yemeni Reduction, by wt P0100111.
Diurethyi benzyl laui'yl ammonium chloride 0. 002 77 l)o. 0.0m 35 (etyl irimethyl ammonium bromide 0. 002 40 Dow... 0.00i l2 stem-y! dimethyl b -nzyl ammonium chloride 0. 0025 00 i)o.. 0.0Ul25 [i0 liutcne bis(nonyl benzyl dimethyl ammonium chloride)..... 0.001 09 Do 0.0005 137 liuiync bis 2 octyl benzy ethyl animoninm chloride) 0. 001 01 Do... 0.0005 00 Butane bis(nonyl benzyl dimethyl ami 84 mouiuin chloride) 0. 001
Do 0.0005 i 5::
It will be seen from the data in the above table that the double, long-chain quaternary ammonium salts employed in the practice of the present invention are much more effective inhibitors than are the conventional quaternary ammonium salts.
Ortho-xylylene bislcetyl dimethyl ammonium bromide) was added in an amount of 0.002 weight per cent to a fifty-fifty mixture of West Texas crude oil and West Texas brine which had been saturated with hydrogen sulfide. The hydrogen sulfide-saturated mixture then had mild carbon steel coupons immersed in it thirty-one times a minute for a period of fourteen days. After the period indicated, it was found that the coupons in the corrosive solution which contained orthoxylylene bis(cetyl dimethyl ammonium bromide) had been corroded at an average rate of 0.00075 inch per year. Metal coupons were also immersed in the corrosive solution to which ortho-xylylene bisicetyl dimethyl ammonium bromide) had not been added. After a similar treatment of immersions over the same period of time it was found that the metal coupons in the corrosive solution to which no inhibitor had been added had been corroded to an extent of 0.0261 inch per year. Thus, the orthoxylylene bis(cetyl dimethyl ammonium bromide) reduced the corrosion rate of the corrosive solution by 97%.
It will be seen from the foregoing data that I have discovered that beneficial effects are obtainable by the double, long-chain quaternary salts, as described above. I have discovered that these compounds are effective in protecting ferrous metal surfaces in contact with corrosive fluids by incorporating or applying to the ferrous metal surfaces an effective amount of the double. long-chain quaternary ammonium salts identified before.
The nature and objects of the present invention having been completely described and illustrated, what I wish to claim as new and useful and to secure by Letters Patent is:
1. A process for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises incorporating in said corrosive solution an effective amount of a double, longchain quaternary ammonium salt represented by the formula:
where R is a radical selected from the group consisting of the radicals having an alkyl chain containing at least 8 carbon atoms and an alkyl chain having at least 8 carbon atoms and a benzyl group; R1 is selected from the group consisting of the alkyl radicals having no more than 2 carbon atoms and the benzyl group radicals; A is selected from the group consisting of normal hydrocarbon chains having from 4 to 16 methylens groups, aryl radicals, and alkyl substituted aryl radicals; and X is a halogen selected from the group consisting of chlorine, bromine, and iodine.
2. A process for preventing the corrosion of ferrous metals exposed to a corrosive solution including a hydrocarbon and water which comprises incorporating in said corrosive solution an effective amount of a double, long-chain quaternary ammonium salt represented by the formula:
where R is a radical selected from the group consisting of the radicals having an alkyl chain containing at least 8 carbon atoms and an alkyl chain having at least 8 carbon atoms and a benzyl group; R1 is selected from the group consisting of the alkyl radicals having no more than 2 carbon atoms and the benzyl group radicals; A is selected from the group consisting of normal hydrocarbon chains having from 4 to 16 methylene groups, aryl radicals, and alkyl substituted aryl radicals; and X is a halogen selected from the group consisting of chlorine, bromine, and iodine.
3. A method for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises incorporating in said corrosive solution an effective amount of decamethylene bis dimethyl cetyl ammonium bromide).
4. A process for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises incorporating in said corrosive solution an effective amount of tetramethylene bis(dimethyl cetyl ammonium bromide).
5. A process for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises incorporating in said corrosive solution an effective amount of butene bisfnonyl benzyl dimethyl ammonium chloride).
6. A process for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises incorporating in said corrosive solution an effective amount of butyne bis12 octyl benzyl diinethyl ammonium chloride).
'7. A process for preventing the corrosion of ferrous metals which comprises incorporating in said corrosive solution an effective amount of butane bis(nonyl benzyl dimethyl ammonium chloride).
8. A process for preventing corrosion in oil and gas Well equipment which comprises the step of injecting into the well an effective amount of a double, long-chain quaternary ammonium salt represented by the formula:
where R is a radical selected from the group consisting of the radicals having an alkyl chain containing at least 8 carbon atoms and an alkyl chain having at least 8 carbon atoms and a benzyl group; R1 is selected from the group consisting of the alkyl radicals having no more than 2 carbon atoms and the benzyl group radicals; A is selected from the group consisting of normal hydrocarbon chains having from 4 to 16 methylene groups, aryl radicals and alkyl substituted aryl radicals; and X is a halogen selected from the group consisting of chlorine, bromine, and iodine.
9. A process for preventing the corrosion of oil and gas well equipment which comprises incorporating into a well fluid an effective amount of a double, long-chain quaternary ammonium salt represented by the formula:
wherev R is a radical selected from the group consisting of the radicals having an alkyl chain containing at least 8 carbon atoms and an alkyl chain having at least 8 carbon atoms and a benzyl group; R1 is selected from the group consisting of the alkyl radicals having no more than 2 carbon atoms and the benzyl group radicals; A is selected from the group consisting of normal hydrocarbon chains having from 4 to 16 methylene groups, aryl radicals, and alkyl sub stituted aryl radicals; and X is a halogen selected from the group consisting of chlorine. bromine, and iodine.
10. A method for preventing corrosion of oil and gas well equipment which comprises injecting into the well an effective amount of decamethylene bisl'dimethyl cetyl ammonium bromide).
11. A method for preventing corrosion of oil and gas well equipment which comprises injecting into the well an effective amount of tetra methylene bisidimethyl cetyl ammonium bromide).
12. A method for preventing corrosion of oil and gas well equipment which comprises inject ing into the well an eflective amount of butene bisinonyl bcnzyl dimethyl ammonium chloride).
13. A method for preventing corrosion of oil and gas well equipment which comprises injecting into the well an effective amount of butyne bis(2 octyl bcnzyl dimethyl ammonium chloride).
14. A method for preventing corrosion of oil and gas well equipment which comprises injecting into the well an effective amount of butane bismonyl benzyl dimethyl ammonium chloride).
15. A process for preventing the corrosion of ferrous metals exposed to a corrosive solution which comprises applying to said metals a double, longchain quaternary ammonium salt rep resented by the formula:
where R is a radical selected from the group consisting of the radicals having an alkyl chain containing at least 8 carbon atoms and an alkyl chain having at least 8 carbon atoms and a benzyl group; R1 is selected from the group consisting of the alkyl radicals having no more than 2 carbon atoms and the benzyl group radicals; A is selected from the group consisting of normal hydrocarbon chains having from 4 to 15 methylene groups, aryl radicals and alkyl substituted aryl radicals; and X i a halogen selected from the group consisting of chlorine, bromine, and iodine.
16. A process in accordance with claim 1 in which the effective amount of the double, longchain quaternary ammonium salt is in the range from about 0.0001% to about 0.005% by weight of the corrosive solution.
17. A process in accordance with claim 2 in which the effective amount of the double, longchain quaternary ammonium salt is in the range from about 0.0001% to about 0.005% by weight of the corrosive solution.
18. A process in accordance with claim 8 in which the effective amount of the double, longchain quaternary ammonium salt is in the range from about 0.000l% to about 0.005% by weight of a corrosive fluid in said well.
19. A process in accordance with claim 9 in which the effective amount of the double, longchain quaternary ammonium salt is in the range from about 0.0001% to about 0.005% by weight of the well fluid.
20JA process in accordance with claim 15 in which an amount in the range from about 0,0001% to about 0.005% by Weight of the dou 'b-le, long-chain quaternary ammonium salt based on the corrosive solution is applied to said metals.
llflELBA L. LYTLE.
References Cited in the file Of this patent UNITED STATES PATENTS Number Name Date 2,460,259 Kahler Jan. 25, 1949 2,525,777 Benneville Oct. 17, 1950 2,525,778 Benneville et a1. Oct. 17, 1950 2,525,779 Benneville et al. Oct. 17, 1950 2,583,399 Wachter et a1. Jan. 22, 1952 2,596,273 Moyer et al. May 13, 1952 2,598,213 Blair May 27, 1952 OTHER REFERENCES Latter, Corrosion Control in Water-Flooding, Article in World Oil, January 1951, Production Section, pages 141, 142, and 144.
Shock et al., Prediction of Corrosion in Oil and Gas Wells, Article in The Petroleum Engineer, Reference Annual, 1951, pages B86, B88, B90, B92, B94, B96, and B98.

Claims (1)

1. A PROCESS FOR PREVENTING THE CORROSION OF FERROUS METALS EXPOSED TO A CORROSIVE SOLUTION WHICH COMPRISES INCORPORATING IN SAID CORROSIVE SOLUTION AN EFFECTIVE AMOUNT OF A DOUBLE, LONGCHAIN QUATERNARY AMMONIUM SALT REPRESENTED BY THE FORMULA:
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Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2745809A (en) * 1953-04-14 1956-05-15 Dow Chemical Co Method and composition for combating corrosion
US2761842A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761835A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761841A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761839A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761837A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761843A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761840A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761838A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761836A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2814593A (en) * 1953-12-18 1957-11-26 Gen Aniline & Film Corp Corrosion inhibition
US2861874A (en) * 1954-06-23 1958-11-25 Alox Corp Corrosion inhibitor for light petroleum solvents and fuels
US2888400A (en) * 1954-04-20 1959-05-26 Nat Aluminate Corp Process for preventing corrosion
US2901430A (en) * 1953-11-06 1959-08-25 Gen Aniline & Film Corp Corrosion inhibition
US2952635A (en) * 1957-03-29 1960-09-13 Geigy Chem Corp Process for preventing corrosion of ferrous metals and composition therefor
US3197301A (en) * 1963-01-04 1965-07-27 Fmc Corp Liquid fertilizers inhibited against corrosion
DE1270877B (en) * 1960-07-28 1968-06-20 Standard Oil Co Mineral oil-based fuels and fuels
EP0565371A2 (en) * 1992-04-08 1993-10-13 Betz Europe, Inc. Boiler double buffers
WO1998023792A1 (en) * 1996-11-28 1998-06-04 Henkel Kommanditgesellschaft Auf Aktien Method for protecting metal surfaces against corrosion in liquid or gaseous media
US20060180794A1 (en) * 2005-02-15 2006-08-17 Goddard Richard J Polyamine-based corrosion inhibitors

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2460259A (en) * 1946-01-22 1949-01-25 W H And L D Betz Method of protecting systems for transporting media corrosive to metal
US2525779A (en) * 1949-06-29 1950-10-17 Rohm & Haas Alkane bis quaternary ammonium salts
US2525778A (en) * 1949-06-29 1950-10-17 Rohm & Haas 1, 4-but-2-yne bis quaternary ammonium halides
US2525777A (en) * 1949-06-29 1950-10-17 Rohm & Haas Butenylene bis
US2583399A (en) * 1951-03-05 1952-01-22 Shell Dev Corrosion prevention method
US2596273A (en) * 1947-09-11 1952-05-13 Cities Service Oil Co Method of inhibiting hydrogen sulfide corrosion of metals
US2598213A (en) * 1949-09-01 1952-05-27 Petrolite Corp Process for preventing corrosion and corrosion inhibitors

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2460259A (en) * 1946-01-22 1949-01-25 W H And L D Betz Method of protecting systems for transporting media corrosive to metal
US2596273A (en) * 1947-09-11 1952-05-13 Cities Service Oil Co Method of inhibiting hydrogen sulfide corrosion of metals
US2525779A (en) * 1949-06-29 1950-10-17 Rohm & Haas Alkane bis quaternary ammonium salts
US2525778A (en) * 1949-06-29 1950-10-17 Rohm & Haas 1, 4-but-2-yne bis quaternary ammonium halides
US2525777A (en) * 1949-06-29 1950-10-17 Rohm & Haas Butenylene bis
US2598213A (en) * 1949-09-01 1952-05-27 Petrolite Corp Process for preventing corrosion and corrosion inhibitors
US2583399A (en) * 1951-03-05 1952-01-22 Shell Dev Corrosion prevention method

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2745809A (en) * 1953-04-14 1956-05-15 Dow Chemical Co Method and composition for combating corrosion
US2901430A (en) * 1953-11-06 1959-08-25 Gen Aniline & Film Corp Corrosion inhibition
US2814593A (en) * 1953-12-18 1957-11-26 Gen Aniline & Film Corp Corrosion inhibition
US2888400A (en) * 1954-04-20 1959-05-26 Nat Aluminate Corp Process for preventing corrosion
US2861874A (en) * 1954-06-23 1958-11-25 Alox Corp Corrosion inhibitor for light petroleum solvents and fuels
US2761837A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761843A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761840A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761838A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761836A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761839A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761841A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761835A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2761842A (en) * 1954-11-18 1956-09-04 Gulf Research Development Co Treatment of clays
US2952635A (en) * 1957-03-29 1960-09-13 Geigy Chem Corp Process for preventing corrosion of ferrous metals and composition therefor
DE1270877B (en) * 1960-07-28 1968-06-20 Standard Oil Co Mineral oil-based fuels and fuels
US3197301A (en) * 1963-01-04 1965-07-27 Fmc Corp Liquid fertilizers inhibited against corrosion
EP0565371A2 (en) * 1992-04-08 1993-10-13 Betz Europe, Inc. Boiler double buffers
EP0565371A3 (en) * 1992-04-08 1994-04-13 Betz Europ Inc
WO1998023792A1 (en) * 1996-11-28 1998-06-04 Henkel Kommanditgesellschaft Auf Aktien Method for protecting metal surfaces against corrosion in liquid or gaseous media
US6261346B1 (en) 1996-11-28 2001-07-17 Cognis Deutschland Gmbh Method for protecting metal surfaces against corrosion in liquid or gaseous media
US20060180794A1 (en) * 2005-02-15 2006-08-17 Goddard Richard J Polyamine-based corrosion inhibitors

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