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US3190733A - Corrosion inhibitor - Google Patents

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Publication number
US3190733A
US3190733A US57402A US5740260A US3190733A US 3190733 A US3190733 A US 3190733A US 57402 A US57402 A US 57402A US 5740260 A US5740260 A US 5740260A US 3190733 A US3190733 A US 3190733A
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Prior art keywords
acid
quaternary
corrosion
inhibitor
dimer
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Expired - Lifetime
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US57402A
Inventor
Jr Olen L Riggs
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ConocoPhillips Co
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Continental Oil Co
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Priority to US57402A priority Critical patent/US3190733A/en
Priority to GB28814/61A priority patent/GB922451A/en
Priority to DEC25096A priority patent/DE1185036B/en
Application granted granted Critical
Publication of US3190733A publication Critical patent/US3190733A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • C—CHEMISTRY; METALLURGY
    • C23—COATING 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
    • C23F—NON-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
    • C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10—Inhibiting 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
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/18—Organic compounds containing oxygen
    • C10L1/188—Carboxylic acids; metal salts thereof
    • C10L1/1881—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
    • C10L1/1883—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom polycarboxylic acid
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/22—Acids obtained from polymerised unsaturated acids
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
    • C10M2215/26—Amines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2070/00—Specific manufacturing methods for lubricant compositions
    • C10N2070/02—Concentrating of additives

Definitions

  • This invention relates to compositions for inhibiting corrosion.
  • the invention relates to two component corrosion inhibiting compositions suitable for use in hydrocarbon systems.
  • a high resistance to rust or corrosion is important in the use of hydrocarbon fuels or lubricants which are in contact with metal surfaces in the presence of water.
  • Fuels for internal combustion engines areexamples of materials which desirably have incorporated therein an additive which provides corrosion inhibiting properties.
  • inhibitors are frequently employed in the processing and transporting of a wide variety of hydrocarbon fractions, for example, in storage tanks, fractionators, pipe lines, transport vessels, etc. Water is almost always present as a contaminant in the processing and storage of hydrocarbon oils; thus the problem of corrosion is always present.
  • the foregoing objects are achieved broadly by providing a corrosion inhibiting composition containing a dimerized fatty acid and a quaternary ammonium c0In-' pound.
  • the invention comprises hydrocarbon oils containing said corrosion inhibiting composition.
  • Dimerized fatty acids which are employed in the compositions of this invention have the general formula:
  • dimers of dienoic acid such as the dimers of sorbic acid, palmitoleic acid, linoleic acid, and eicosadienoic acid
  • dimers of trienoic acids such as dimers of linolenic acid and eleostearic acid.
  • R is an alkyl group containing 6-15 carbon atoms
  • R is aryl
  • R s are alkyl groups containing 14 carbon atoms
  • Y is a halogen
  • quaternary ammonium compounds include materials such as dodecylbenzyl trimethyl ammonium chloride, heptylbenzyl triethyl ammonium chloride, heptylbenzyl triethyl ammonium bromide, octylnaphthylmethyl tributyl ammonium chloride, octylbenzyl trimethyl ammonium bromide, octylbenzyl tripropyl ammonium chloride, nonylbenzyl trimethyl ammonium chloride, nonylnaphhylmethyl triethyl ammonium chloride, nonylbenzyl triethyl ammonium bromide, hexylbenzyl trimethyl ammonium chloride, octylnaphthylmethyl triethyl ammonium'chloride, tridecylbenzyl tri-.
  • propyl ammonium chloride and hexylbenzyl tripropyl ammonium chloride.
  • the preferred material is dodecylbenzyl trimethyl ammonium chloride. This compound is prepared by chloromethylating dodecylbenzene to dodecylbenzyl chloride followed by reaction with trimethyl amine to obtain the final quaternary product.
  • the relative quantities 'of the two components em ployed in the inhibitor can vary over a wide range
  • dimerized acid is present in the composition in an amount from about 92 to about percent by weight. employed in the composition in an amount between about and percent by weight.
  • the inhibitor compositions of this invention can be employed generally for the prevention of corrosion in systems containing hydrocarbon oils. They can be employed with heavy fuel various heating oils, naphthas, gasolines, individual hydrocarbons.
  • the inhibitor is present in an amount between about 1 and about 500 parts per million by weight. Larger amounts of inhibitor can be employed; however they usually are not necessary.
  • the inhibitor compositions can be prepared in any conventional manner, for example, the acid can be added to the quaternary or vice versa. Also the combination of the inhibitor with the hydrocarbon oil can be effected in any suitable manner. If desired, either of the components of the inhibitor composition can first be added to the hydrocarbon oil and then the other component.
  • EXAMPLE 1 500 ml. of gasoline was placed in a test vessel with. 50 ml. of brine. A mild steel coupon was extended vertically in the gasoline brine mixture which was agitated. The temperature of the mixture was increased to F. where it was maintained for 96 hours. The results of the test are presented in Table I.
  • the dimer acid component is Weight Corrosion Loss, Rate,
  • n varies from 10 to 42 and x varies from 6 to 10 and a quaternary ammonium compound having the formula:
  • R is an alkyl group containing 6-15 carbon atoms
  • R is aryl
  • R s are alkyl groups containing 1-4 carbon atoms
  • Y is a halogen.
  • composition of claim 1 containing from about to about weight percent acid.
  • composition of claim 2 in which the quaternary ammonium compound is dodecylbenzyl trimethyl ammonium chloride.
  • composition of claim 3 in which the acid is 9,11 octadecadienoic.
  • a composition comprising a major proportion of hydrocarbon oil and between about 1 and about 500 parts per million by weight based on the hydrocarbon oil of a corrosion inhibitor consisting essentially of from about 92 to 60 percent by weight of an acid having the formula:
  • n varies from 10 to 42 and x varies from 6 to 10 and a quaternary ammonium compound having the formula:
  • R is an alkyl group containing 6-15 carbon atoms
  • R is aryl
  • R s are alkyl groups containing 1-4 carbon atoms
  • Y is a halogen.
  • composition of claim 5 in which the inhibitor is present in an amount between about 1 and 500 parts per million by weight based on the hydrocarbon oil and in which the inhibitor contains between about 80 and 90 weight percent acid.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
  • Lubricants (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Description

United States Patent 3,190,733 CORRDSION INHIBITOR Olen L. Riggs, Jr., Ponca City, Okla, assignor to Continental Oil Company, Ponca City, Okla., a corporation of Delaware r No Drawing. Filed Sept. '21, 1960, Ser. No. 57,402
7 Claims. (Cl. 4470) This invention relates to compositions for inhibiting corrosion. In one aspect, the invention relates to two component corrosion inhibiting compositions suitable for use in hydrocarbon systems.
A high resistance to rust or corrosion is important in the use of hydrocarbon fuels or lubricants which are in contact with metal surfaces in the presence of water. Fuels for internal combustion engines areexamples of materials which desirably have incorporated therein an additive which provides corrosion inhibiting properties.
In addition, inhibitors are frequently employed in the processing and transporting of a wide variety of hydrocarbon fractions, for example, in storage tanks, fractionators, pipe lines, transport vessels, etc. Water is almost always present as a contaminant in the processing and storage of hydrocarbon oils; thus the problem of corrosion is always present.
It is an object of thisjnvention to provide corrosion inhibiting compositions which are suitable for use with hydrocarbon oils.
It is another object of this invention to provide corrosion inhibiting compositions for use in hydrocarbons which are in contact with metals in the presence of water and other corrosive materials.
These and other objects of the invention will become more readily apparent from the detailed description and discussion.
The foregoing objects are achieved broadly by providing a corrosion inhibiting composition containing a dimerized fatty acid and a quaternary ammonium c0In-' pound. In one aspect, the invention comprises hydrocarbon oils containing said corrosion inhibiting composition.
Dimerized fatty acids which are employed in the compositions of this invention have the general formula:
wherein It varies from 10 to 42 and x varies from 6 to 10.
Specific acids which can be employed include dimers of dienoic acid, such as the dimers of sorbic acid, palmitoleic acid, linoleic acid, and eicosadienoic acid; also dimers of trienoic acids, such as dimers of linolenic acid and eleostearic acid.
The quaternary ammonium compounds which make up the other component of the inhibiting composition are described by the general formula as follows:
wherein R is an alkyl group containing 6-15 carbon atoms, R is aryl, R s are alkyl groups containing 14 carbon atoms, and Y is a halogen.
Specific examples of the quaternary ammonium compounds include materials such as dodecylbenzyl trimethyl ammonium chloride, heptylbenzyl triethyl ammonium chloride, heptylbenzyl triethyl ammonium bromide, octylnaphthylmethyl tributyl ammonium chloride, octylbenzyl trimethyl ammonium bromide, octylbenzyl tripropyl ammonium chloride, nonylbenzyl trimethyl ammonium chloride, nonylnaphhylmethyl triethyl ammonium chloride, nonylbenzyl triethyl ammonium bromide, hexylbenzyl trimethyl ammonium chloride, octylnaphthylmethyl triethyl ammonium'chloride, tridecylbenzyl tri-.
propyl ammonium chloride, and hexylbenzyl tripropyl ammonium chloride. Of the quaternary. ammonium compounds, the preferred material is dodecylbenzyl trimethyl ammonium chloride. This compound is prepared by chloromethylating dodecylbenzene to dodecylbenzyl chloride followed by reaction with trimethyl amine to obtain the final quaternary product.
The relative quantities 'of the two components em ployed in the inhibitor" can vary over a wide range;
however usually the dimerized acid is present in the composition in an amount from about 92 to about percent by weight. employed in the composition in an amount between about and percent by weight.
. The inhibitor compositions of this invention can be employed generally for the prevention of corrosion in systems containing hydrocarbon oils. they can be employed with heavy fuel various heating oils, naphthas, gasolines, individual hydrocarbons.
'For example, 'ils, diesel oils, etc., or with Only small amounts of the corrosion inhibitor are required in combination with the hydrocarbon oil. For example, usually the inhibitor is present in an amount between about 1 and about 500 parts per million by weight. Larger amounts of inhibitor can be employed; however they usually are not necessary.
The inhibitor compositions can be prepared in any conventional manner, for example, the acid can be added to the quaternary or vice versa. Also the combination of the inhibitor with the hydrocarbon oil can be effected in any suitable manner. If desired, either of the components of the inhibitor composition can first be added to the hydrocarbon oil and then the other component.
It has been found that the combination of the dimer acid and the quaternary ammonium compound provides a synergistic effect in that the combination provides better corrosion resistance than either of the individual components, The efficacy of the compositions in preventing corrosion is even more unexpected, since the quaternary compounds exhibit little or no corrosive in hibition effects and may even cause corrosion when used alone.
The following examples are presented in illustration of the invention:
EXAMPLE 1 500 ml. of gasoline was placed in a test vessel with. 50 ml. of brine. A mild steel coupon was extended vertically in the gasoline brine mixture which was agitated. The temperature of the mixture Was increased to F. where it was maintained for 96 hours. The results of the test are presented in Table I.
Preferably, the dimer acid component is Weight Corrosion Loss, Rate,
gm. m.p.y.
Petroleum Fraction Inhibitor, 25 ppm.
High Test Gasline None Do Ethylene Dlamine Sulfonate. Dimer A 1 Quaternary 2 Dimer A Quaternary.
9,11 Octadecadienoic acid. 2 Dodecylbenzyl trimethyl ammonium chloride.
It is apparent from the table that the combination of dimer acid and quaternary compound (90 percent acid and percent quaternary by weight) provide substantially better results than either of these materials when used individually. The results are unusual when it is considered that the quaternary compound actually was corrosive, since it causes a greater corrosion rate than no inhibitor. It is noted also that the combination of dimer acid and quaternary provide better results than a known corrosion inhibitor, ethylene diamine sulfonate.
EXAMPLE 2 An additional test was carried out utilizing the same procedure employed in Example 1 but with a different dimer acid. The results of tlu's test are presented in Table II.
Table II Corrosion Rate, m.p.y.
Petroleum Fraction Inhibitor, ppm.
Dimer B 1 Quaternary 2 Dimer B Plus Quaternary. Dimer 0 Plus Quaternary.
Hlgh Test Gasoline Do 1 An acid dimer having the following properties:
Specific gravity at 60l60 F 0. 884 Viscosity- SUS 210 F 52 SUS 100 F Flash Point F. (0.0.0.) A.S.'I.M. Color A.S.T.M. Pour Point F 2 Dodeeylbenzyl trimethyl ammonium chloride. 3 Mixture oi dimer and trimer of octadecadicnoic acid.
wherein n varies from 10 to 42 and x varies from 6 to 10 and a quaternary ammonium compound having the formula:
wherein R is an alkyl group containing 6-15 carbon atoms, R is aryl, R s are alkyl groups containing 1-4 carbon atoms, and Y is a halogen.
2. The composition of claim 1 containing from about to about weight percent acid.
3. The composition of claim 2 in which the quaternary ammonium compound is dodecylbenzyl trimethyl ammonium chloride.
4. The composition of claim 3 in which the acid is 9,11 octadecadienoic.
5. A composition comprising a major proportion of hydrocarbon oil and between about 1 and about 500 parts per million by weight based on the hydrocarbon oil of a corrosion inhibitor consisting essentially of from about 92 to 60 percent by weight of an acid having the formula:
wherein n varies from 10 to 42 and x varies from 6 to 10 and a quaternary ammonium compound having the formula:
wherein R is an alkyl group containing 6-15 carbon atoms, R is aryl, R s are alkyl groups containing 1-4 carbon atoms, and Y is a halogen.
6. The composition of claim 5 in which the inhibitor is present in an amount between about 1 and 500 parts per million by weight based on the hydrocarbon oil and in which the inhibitor contains between about 80 and 90 weight percent acid.
7. The composition of claim 6 in which the hydrocarbon oil is gasoline, the dimer acid is the dimer of 9,11 octadecadienoic acid, and the quaternary ammonium compound is dodecylbenzyl trimethyl ammonium chloride.
References Cited by the Examiner UNITED STATES PATENTS 2,632,695 3/53 Landis et a1. 4466 2,676,987 4/54 Lewis et a1. 252-390 2,745,809 5/56 Cardwell et a1. 252-855 2,861,874 11/58 OKelly et a1. 4466 FOREIGN PATENTS 798,620 7/58 Great Britain.
DANIEL E. WYMAN, Primary Examiner.
JULIUS GREENWALD, JOSEPH R. LIBERMAN,
ALPHONSO D. SULLIVAN, Examiners.

Claims (1)

  1. 5. A COMPOSITION COMPRISING A MAJOR PROPORTION OF HYDROCARBON OIL AND BETWEEN ABOUT 1 AND ABOUT 500 PARTS PER MILLION BY WEIGHT BASED ON THE HYDROCARBON OIL OF A CORROSION INHIBITOR CONSISTING ESSENTIALLY OF FROM ABOUT 92 TO 60 PERCENT BY WEIGHT OF AN ACID HAVING THE FORMULA:
US57402A 1960-09-21 1960-09-21 Corrosion inhibitor Expired - Lifetime US3190733A (en)

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US57402A US3190733A (en) 1960-09-21 1960-09-21 Corrosion inhibitor
GB28814/61A GB922451A (en) 1960-09-21 1961-08-09 Corrosion inhibitor
DEC25096A DE1185036B (en) 1960-09-21 1961-09-19 Corrosion protection agents, in particular for use in hydrocarbons that are in contact with metal surfaces

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3720615A (en) * 1969-08-11 1973-03-13 Kao Corp Oil-soluble rust preventive composition
US5525127A (en) * 1993-12-23 1996-06-11 Ethyl Petroleum Additives Limited Evaporative burner fuels and additives therefor

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3865688D1 (en) * 1987-01-30 1991-11-28 Pumptech Nv METHOD AND COMPOSITION FOR CORROSION INHIBITATION OF IRON AND STEEL.

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2632695A (en) * 1951-09-20 1953-03-24 Socony Vacuum Oil Co Inc Rust inhibitor for light petroleum products
US2676987A (en) * 1950-12-27 1954-04-27 California Research Corp Bis-alkyl benzyl quaternary ammonium salt
US2745809A (en) * 1953-04-14 1956-05-15 Dow Chemical Co Method and composition for combating corrosion
GB798620A (en) * 1956-05-23 1958-07-23 Exxon Standard Sa Additives to prevent the corrosion of apparatus containing hydrocarbons
US2861874A (en) * 1954-06-23 1958-11-25 Alox Corp Corrosion inhibitor for light petroleum solvents and fuels

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2676987A (en) * 1950-12-27 1954-04-27 California Research Corp Bis-alkyl benzyl quaternary ammonium salt
US2632695A (en) * 1951-09-20 1953-03-24 Socony Vacuum Oil Co Inc Rust inhibitor for light petroleum products
US2745809A (en) * 1953-04-14 1956-05-15 Dow Chemical Co Method and composition for combating corrosion
US2861874A (en) * 1954-06-23 1958-11-25 Alox Corp Corrosion inhibitor for light petroleum solvents and fuels
GB798620A (en) * 1956-05-23 1958-07-23 Exxon Standard Sa Additives to prevent the corrosion of apparatus containing hydrocarbons

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3720615A (en) * 1969-08-11 1973-03-13 Kao Corp Oil-soluble rust preventive composition
US5525127A (en) * 1993-12-23 1996-06-11 Ethyl Petroleum Additives Limited Evaporative burner fuels and additives therefor

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DE1185036B (en) 1965-01-07
GB922451A (en) 1963-04-03

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