US3897351A - Lubricant compositions - Google Patents
Lubricant compositions Download PDFInfo
- Publication number
- US3897351A US3897351A US403692A US40369273A US3897351A US 3897351 A US3897351 A US 3897351A US 403692 A US403692 A US 403692A US 40369273 A US40369273 A US 40369273A US 3897351 A US3897351 A US 3897351A
- Authority
- US
- United States
- Prior art keywords
- composition
- accordance
- anhydride
- lubricant
- alkenylsuccinic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 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
- C10M173/00—Lubricating compositions containing more than 10% water
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/082—Inorganic acids or salts thereof containing nitrogen
- C10M2201/083—Inorganic acids or salts thereof containing nitrogen nitrites
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/14—Inorganic compounds or elements as ingredients in lubricant compositions inorganic compounds surface treated with organic compounds
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/022—Well-defined aliphatic compounds saturated
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/024—Well-defined aliphatic compounds unsaturated
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/04—Well-defined cycloaliphatic compounds
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- 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
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- 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
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- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- C10M2215/065—Phenyl-Naphthyl amines
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- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
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- 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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/02—Esters of silicic acids
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/02—Unspecified siloxanes; Silicones
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
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- 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
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- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
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- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
-
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/01—Emulsions, colloids, or micelles
-
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
-
- 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 improved lubricant compositions and, in one of its aspects, relates more particularly to lubricant compositions that are normally susceptible of causing deterioration of metal surfaces with which they may come into contact or tend to undergo deterioration under conditions of use. Still more particularly, in this aspect, the invention relates to lubricant compositions in th form of lubricating oils, greases, or aqueous-base lubricants, which normally exhibit the aforementioned shortcomings in performing their intended functions.
- lubricants including lubricating oils, greases and aqueous-base cutting fluids are susceptible of causing deterioration by oxidation or corrosion when coming into contact with various metal surfaces.
- lubricants may also tend to undergo deterioration in performing their intended functions, for example, in the impairment of load-carrying characteristics, thus clearly indicating the necessity for incorporating in such lubricants effective anti-oxidative and corrosion inhibiting improving agents.
- machining operations of metals such as cutting, grinding, turning, milling and the like where it is customary to flood the tool and the work with a coolant for the purpose of carrying off heat which is produced during the operation. It is also customary to employ these coolants in combination with various agents having lubricating and extreme-pressure properties for reducing friction between the tool and work-piece, particularly in operations such as tapping and broaching.
- aqueous compositions containing such lubricating agents as emulsified petroleum or nonpetroleum additives.
- aqueous cutting fluids In order for such aqueous cutting fluids to perform satisfactorily, is the requirement that residual deposits on the tool and the work following the machining operation are avoided.
- amine salt of the re action product of at least one member of the group consisting of alkyl and alkenylsuccinic anhydrides and at least one member of the group consisting of benzotriazole and substituted benzotriazoles, in a mole ratio of from 1:1 to 1:2.
- these amine salts are employed in an amount of from about 0.001 to about 40%, and preferably, in an amount from about 0.5 to about 10%, by weight, of the total lubricant composition.
- the amine and the aforementioned reaction product are reacted in a mole ratio of about 1:1.
- the lubricant may comprise many mineral or synthetic oils of lubricating viscosity.
- mineral oil at a viscosity of at least 40 SSU at l00F. and particularly those falling within the range from about 60 SSU to about 6000 SSU at F. is preferably employed.
- various compounds of this type may be successfully utilized.
- Typical synthetic vehicles include: polypropylene glycol, trimethylol propane esters, neopentyl and pentaerythritol esters, di-(2-ethyl hexyl) sebacate, di-(Z-ethyl hexyl) adipate, dibutyl phthalate, fluorocarbons, silicate esters, silanes, esters of phosphorous-containing acids, liquid ureas, ferrocene derivatives, hydrogenated mineral oils, chain-type polyphenyls, siloxanes and silicones (polysilioxanes), alkyl-substituted diphenyl ethers typified by a butyl-substituted bis (p-phenoxy phenyl) ether, phenoxy phenyl ethers, etc.
- the aforementioned liquid hydrocarbon lubricants may also be employed in combination with a grease forming quantity of a thickening agent as vehicles in the production of greases containing the abovedescribed amine salts.
- a thickening or gelling agents may include any of the conventional metal salts or soaps, which are dispersed in the lubricating vehicle in grease-forming quantities, in such degree as to impart to the resulting grease composition, the desired consistency.
- Other thickening agents that may be employed in the grease formation may comprise the nonsoap thickeners, such as surface-modified clays and silicas, aryl ureas, calcium complexes and similar materials.
- grease thickeners may be employed which do not melt and dissolve when used at the required temperature within a particular environment; however, in all other respects, any material which is normally employed for thickening or gelling hydrocarbon fluids for forming grease can be used in preparing the aforementioned improved grease in accordance with the present invention.
- Any amine may be employed for forming the salt of the aforementioned reaction product of at least one member of the group consisting of alkyl and alkenylsuccinic anhydrides and at least one member of the group consisting of benzotriazole and substituted benzotriazoles.
- alkanolamines are most advantageously employed and may be of any molecular weight.
- these amines should be liquid at room temperature.
- the lower molecular weight amines are generally preferred and for this purpose, it has been found that such alkanolamines as mono-, dior tri-ethanolamine are most effective.
- the amines may be water soluble or oil soluble and may,
- alkanolamines as isopropanolamines, e.g. mono-, diand triisopropanolamine, di-methylethanolamine, diethylethanolamine, aminoethylethanolamine, N-acetyl ethanolamine, phenylethanolamine, phenyldiethanolamine, and mixtures thereof.
- any alkyl or alkenylsuccinic anhydride may be employed for reaction with benzotriazole or substituted benzotriazoles in producing the aforementioned reacbenzotriazole reaction product, the junction corrosion test results dropped to 62 microamps, as shown in Example 4, and indicating that this additive system is considered satisfactory for machining a nonferrous metal such as magnesium without corrosion problems associated with steel contact on the machine tool.
- examples l, 2 and 3 typical formulations considered unsatisfactory for nonferrous metal machining are represented by examples l, 2 and 3.
- example 1 there is employed a 43%, by weight, aqueous triethanolamine solution, which is found to stain magnesium and results in a 295 microamp current reading. If an amine is combined to form a salt of benzotriazole and tetrapropenylsuccinic acid, respectively, in examples 2 and 3, the current values still exceed 120 microamps.
- composition in accordance with claim 1 wherein said lubricant comprises an oil of lubricating viscosity.
- composition in accordance with claim 1 wherein said lubricant comprises a grease.
- composition in accordance with claim 1 wherein said lubricant comprises water in major proportion.
- composition in accordance with claim 1 wherein the alkenylsuccinic anhydride is octenylsuccinic anhydride.
- a composition in accordance with claim 1 wherein the alkenylsuccinic anhydride is polybutenylsuccinic anhydride.
- a composition in accordance with claim 1 wherein the alkenylsuecinic anhydride is triacontenylsuccinic anhydride.
- a composition in accordance with claim 1 wherein the alkenylsuccinic anhydride is isooctadecylsuccinic anhyride.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
Lubricant compositions are provided containing a corrosioninhibiting amount of an amine salt of the reaction product of at least one member of the group consisting of alkyl and alkenylsuccinic anhydrides and at least one member of the group consisting of benzotriazole and substituted benzotriazoles in a mole ratio of from 1:1 to 1:2.
Description
United States Patent Davis et al.
[451 July 29, 1975 LUBRICANT COMPOSITIONS Inventors: Robert H. Davis, Pitman; John W.
Schick, Cherry Hill, both of NJ.
Assignee'. Mobil Oil Corporation, New York,
Filed: Oct. 4, 1973 Appl. No.: 403,692
US. Cl. 252/34; 252/493; 252/390;
260/308 B Int. Cl ClOm 1/32 Field of Search 252/34, 49.3, 390
References Cited UNlTED STATES PATENTS 6/1966 Davis 252/34 FOREIGN PATENTS OR APPLICATIONS 1,444,903 1 H1968 Germany Primary Examiner-Helen M. S. Sneed Attorney, Agent, or Firm-Charles A. Huggett; Raymond W. Barclay; Benjamin 1. Kaufman ABSTRACT 12 Claims, No Drawings l LUBRICANT COMPOSITIONS BACKGROUND OF THE INVENTION 1. Field of the Invention.
This invention relates to improved lubricant compositions and, in one of its aspects, relates more particularly to lubricant compositions that are normally susceptible of causing deterioration of metal surfaces with which they may come into contact or tend to undergo deterioration under conditions of use. Still more particularly, in this aspect, the invention relates to lubricant compositions in th form of lubricating oils, greases, or aqueous-base lubricants, which normally exhibit the aforementioned shortcomings in performing their intended functions.
2. Description of the Prior Art.
It is well known that certain types of lubricants, including lubricating oils, greases and aqueous-base cutting fluids are susceptible of causing deterioration by oxidation or corrosion when coming into contact with various metal surfaces. In addition, such lubricants may also tend to undergo deterioration in performing their intended functions, for example, in the impairment of load-carrying characteristics, thus clearly indicating the necessity for incorporating in such lubricants effective anti-oxidative and corrosion inhibiting improving agents.
Of particular significance, is the machining operations of metals, such as cutting, grinding, turning, milling and the like where it is customary to flood the tool and the work with a coolant for the purpose of carrying off heat which is produced during the operation. It is also customary to employ these coolants in combination with various agents having lubricating and extreme-pressure properties for reducing friction between the tool and work-piece, particularly in operations such as tapping and broaching. In this respect, it has heretofore been the practice to employ for such purpose aqueous compositions containing such lubricating agents as emulsified petroleum or nonpetroleum additives. In order for such aqueous cutting fluids to perform satisfactorily, is the requirement that residual deposits on the tool and the work following the machining operation are avoided. Other important requirements include tolerance in hard water solutions so that precipitation of lubricant components will not occur and that tacky residues which interfere with the operation of the machine, as well as excessive foam formation are avoided. Cutting fluids, known prior to the present invention, have not, however, satisfactorily met the foregoing requirements.
SUMMARY OF THE INVENTION It has now been found that the aforementioned corrosion and oxidative inhibiting properties can be effectively improved by incorporating, in minor proportion corrosion-inhibiting amounts of an amine salt of the re action product of at least one member of the group consisting of alkyl and alkenylsuccinic anhydrides and at least one member of the group consisting of benzotriazole and substituted benzotriazoles, in a mole ratio of from 1:1 to 1:2. For most applications, these amine salts are employed in an amount of from about 0.001 to about 40%, and preferably, in an amount from about 0.5 to about 10%, by weight, of the total lubricant composition. Preferably, the amine and the aforementioned reaction product are reacted in a mole ratio of about 1:1.
Where the lubricant comprises an oil of lubricating viscosity, the lubricant may comprise many mineral or synthetic oils of lubricating viscosity. In instances where high temperature stability is not a prime requirement, mineral oil at a viscosity of at least 40 SSU at l00F. and particularly those falling within the range from about 60 SSU to about 6000 SSU at F. is preferably employed. In instances where the lubricant comprises a synthetic hydrocarbon oil rather than a mineral oil, or in combination therewith, various compounds of this type may be successfully utilized. Typical synthetic vehicles include: polypropylene glycol, trimethylol propane esters, neopentyl and pentaerythritol esters, di-(2-ethyl hexyl) sebacate, di-(Z-ethyl hexyl) adipate, dibutyl phthalate, fluorocarbons, silicate esters, silanes, esters of phosphorous-containing acids, liquid ureas, ferrocene derivatives, hydrogenated mineral oils, chain-type polyphenyls, siloxanes and silicones (polysilioxanes), alkyl-substituted diphenyl ethers typified by a butyl-substituted bis (p-phenoxy phenyl) ether, phenoxy phenyl ethers, etc.
The aforementioned liquid hydrocarbon lubricants may also be employed in combination with a grease forming quantity of a thickening agent as vehicles in the production of greases containing the abovedescribed amine salts. For this purpose, a wide variety of materials may be employed. These thickening or gelling agents may include any of the conventional metal salts or soaps, which are dispersed in the lubricating vehicle in grease-forming quantities, in such degree as to impart to the resulting grease composition, the desired consistency. Other thickening agents that may be employed in the grease formation may comprise the nonsoap thickeners, such as surface-modified clays and silicas, aryl ureas, calcium complexes and similar materials. In general, grease thickeners may be employed which do not melt and dissolve when used at the required temperature within a particular environment; however, in all other respects, any material which is normally employed for thickening or gelling hydrocarbon fluids for forming grease can be used in preparing the aforementioned improved grease in accordance with the present invention.
Any amine may be employed for forming the salt of the aforementioned reaction product of at least one member of the group consisting of alkyl and alkenylsuccinic anhydrides and at least one member of the group consisting of benzotriazole and substituted benzotriazoles. In a preferred modification alkanolamines are most advantageously employed and may be of any molecular weight. Preferably these amines should be liquid at room temperature. The lower molecular weight amines are generally preferred and for this purpose, it has been found that such alkanolamines as mono-, dior tri-ethanolamine are most effective. The amines may be water soluble or oil soluble and may,
therefore, include such alkanolamines as isopropanolamines, e.g. mono-, diand triisopropanolamine, di-methylethanolamine, diethylethanolamine, aminoethylethanolamine, N-acetyl ethanolamine, phenylethanolamine, phenyldiethanolamine, and mixtures thereof.
Any alkyl or alkenylsuccinic anhydride may be employed for reaction with benzotriazole or substituted benzotriazoles in producing the aforementioned reacbenzotriazole reaction product, the junction corrosion test results dropped to 62 microamps, as shown in Example 4, and indicating that this additive system is considered satisfactory for machining a nonferrous metal such as magnesium without corrosion problems associated with steel contact on the machine tool.
Table Aqueous Coolant Galvanic Corrosion Inhibitors Tctrapropcnyl Galvanic Corrosion Test Tetrasuccinic Microamps for Magncsium/ propcnyl Anhydridc/ Steel Couple (Test soln. Triethanolsuccinic Bcnzo- Benzotriazole 40 parts dist. water. Example amine Anhydride triazolc Reaction Product Water I part additive concentrate) hydride and isooctadecylsuccinic anhydride. Typically representative of the substituted benzotriazoles is tolyl triazole. It should also be noted that in addition to imparting corrosion-inhibiting properties to lubricant compositions, the amine salts of the present invention are also effective in imparting anti-wear, anti-rust and bactericidal properties thereto.
DESCRIPTION OF SPECIFIC EMBODIMENTS The following examples and comparative data will serve to illustrate the amine salts of the present invention and to demonstrate their effectiveness in lubricant compositions which are normally susceptible of causing oxidative and corrosive deterioration of metal surfaces with which they may come into contact or tend to undergo deterioration under conditions of use, and particularly with respect to the use of these amine salts in Inbricating oils, greases and water-base lubricants. It will be understood, of course, that it is not intended the invention be limited to the particular compositions disclosed or to the operations or manipulations involved. Various modifications thereof can be employed and will be readily apparent to those skilled in the art.
A series of additive systems were evaluated, as shown in the following table, in accordance with a well-known galvanic corrosion test which provides for a bimetallic magnesium/steel couple separated by a glass cloth strip and shorted with a three inch wire. This couple is immersed in a 40/1 test lubricant-coolant solution. After 24 hours, the shorted wire is replaced with microammeter leads and current is measured. Values in excess of 120 microamps are indicative of severe corrosion and cause for lubricant rejection.
As will be seen from the comparative data of the table typical formulations considered unsatisfactory for nonferrous metal machining are represented by examples l, 2 and 3. In example 1 there is employed a 43%, by weight, aqueous triethanolamine solution, which is found to stain magnesium and results in a 295 microamp current reading. If an amine is combined to form a salt of benzotriazole and tetrapropenylsuccinic acid, respectively, in examples 2 and 3, the current values still exceed 120 microamps. However, if triethanolamine is combined with a tetrapropenylsuccinic acid/- It will be understood that although the present invention has been described with preferred embodiments, various modifications and adaptations thereof may be resorted to without departing from the spirit of the invention as those skilled in the art will readily understand.
We claim:
1. A lubricant composition containing a corrosioninhibiting amount of an alkanolamine salt of the reaction product of at least one member of the group consisting of alkyl and alkenylsuccinic anhydrides and at least one member of the group consisting of benzotriazole and tolyl triazole in a mole ratio of from 1:1 to 1:2.
2. A composition in accordance with claim 1 wherein said lubricant comprises an oil of lubricating viscosity.
3. A composition in accordance with claim 1 wherein said lubricant comprises a grease.
4. A composition in accordance with claim 1 wherein said lubricant comprises water in major proportion.
S. A composition in accordance with claim 1 wherein said alkanolamine salt is present in an amount from about .001 to about 40%, by weight.
6. A composition in accordance with claim 1 wherein said alkanolamine salt is present in an amount from about 0.5 to about 10%, by weight.
7. A composition in accordance with claim 1 wherein said alkanolamine and said reaction product are reacted in a mole ratio of about 1:1.
8. A composition in accordance with claim 1 wherein the alkanolamine is tri-ethanolamine.
9. A composition in accordance with claim 1 wherein the alkenylsuccinic anhydride is octenylsuccinic anhydride.
10. A composition in accordance with claim 1 wherein the alkenylsuccinic anhydride is polybutenylsuccinic anhydride.
11. A composition in accordance with claim 1 wherein the alkenylsuecinic anhydride is triacontenylsuccinic anhydride.
12. A composition in accordance with claim 1 wherein the alkenylsuccinic anhydride is isooctadecylsuccinic anhyride.
Claims (12)
1. A LUBRICANT COMPOSITION CONTAINING A CORROSION-INHIBITING AMOUNG OF AN ALKANOLAMINE SALT OF THE REACTION PRODUCT OF AT LEAST ONE MEMBER OF TE GROUPCONSISTING OF ALKYL AND ALKENYLSUCCINIC ANHYDRIDES AND AT LEAST ONE MEMBER OF THE GROUP CONSISTING OF BENZOTRIAZOLE AND TOLYL TRIAZOLE IN A MOLE RATIO OF FROM 1:1 TO 1:2.
2. A composition in accordance with claim 1 wheRein said lubricant comprises an oil of lubricating viscosity.
3. A composition in accordance with claim 1 wherein said lubricant comprises a grease.
4. A composition in accordance with claim 1 wherein said lubricant comprises water in major proportion.
5. A composition in accordance with claim 1 wherein said alkanolamine salt is present in an amount from about .001 to about 40%, by weight.
6. A composition in accordance with claim 1 wherein said alkanolamine salt is present in an amount from about 0.5 to about 10%, by weight.
7. A composition in accordance with claim 1 wherein said alkanolamine and said reaction product are reacted in a mole ratio of about 1:1.
8. A composition in accordance with claim 1 wherein the alkanolamine is tri-ethanolamine.
9. A composition in accordance with claim 1 wherein the alkenylsuccinic anhydride is octenylsuccinic anhydride.
10. A composition in accordance with claim 1 wherein the alkenylsuccinic anhydride is polybutenylsuccinic anhydride.
11. A composition in accordance with claim 1 wherein the alkenylsuccinic anhydride is triacontenylsuccinic anhydride.
12. A composition in accordance with claim 1 wherein the alkenylsuccinic anhydride is isooctadecylsuccinic anhyride.
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US403692A US3897351A (en) | 1973-10-04 | 1973-10-04 | Lubricant compositions |
GB4192574A GB1465981A (en) | 1973-10-04 | 1974-09-26 | Amine salts of benzotriazole reaction products and their use in lubricants |
CA210,260A CA1039293A (en) | 1973-10-04 | 1974-09-27 | Lubricant compositions |
JP49110686A JPS5065509A (en) | 1973-10-04 | 1974-09-27 | |
ZA00746217A ZA746217B (en) | 1973-10-04 | 1974-09-30 | Lubricant compositions |
IT28037/74A IT1033101B (en) | 1973-10-04 | 1974-10-02 | AMINE SALT-BASED ADDITIVES AND LUBRICANT COMPOSITIONS CONTAINING THEM |
FR7433390A FR2246551B1 (en) | 1973-10-04 | 1974-10-03 | |
NLAANVRAGE7413095,A NL175431C (en) | 1973-10-04 | 1974-10-03 | METHOD FOR PREPARING AN AGENT FOR ANTI-CORROSION LUBRICANTS AND METHOD FOR PREPARING LUBRICANTS |
DE19742447550 DE2447550A1 (en) | 1973-10-04 | 1974-10-04 | AMINE SALT AND ITS USE AS AN ADDITIVE TO LUBRICANTS |
AU74044/74A AU481687B2 (en) | 1973-10-04 | 1974-10-04 | Lubricant compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US403692A US3897351A (en) | 1973-10-04 | 1973-10-04 | Lubricant compositions |
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Publication Number | Publication Date |
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US3897351A true US3897351A (en) | 1975-07-29 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US403692A Expired - Lifetime US3897351A (en) | 1973-10-04 | 1973-10-04 | Lubricant compositions |
Country Status (9)
Country | Link |
---|---|
US (1) | US3897351A (en) |
JP (1) | JPS5065509A (en) |
CA (1) | CA1039293A (en) |
DE (1) | DE2447550A1 (en) |
FR (1) | FR2246551B1 (en) |
GB (1) | GB1465981A (en) |
IT (1) | IT1033101B (en) |
NL (1) | NL175431C (en) |
ZA (1) | ZA746217B (en) |
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4107060A (en) * | 1975-06-17 | 1978-08-15 | Mobil Oil Corporation | Lubricant compositions containing biocidal, antirust additives |
US4153563A (en) * | 1978-05-24 | 1979-05-08 | Mobil Oil Corporation | Lubricant compositions containing benzotriazole-allyl sulfide reaction products |
US4212754A (en) * | 1979-04-23 | 1980-07-15 | Mobil Oil Corporation | Chelate detergent and antiwear additive for lubricants derived from hydroxyalkylated benzotriazoles |
US4255214A (en) * | 1977-11-21 | 1981-03-10 | Falconer Plate Glass Corporation | Methods of manufacturing and protecting mirrors |
DE2943963A1 (en) * | 1979-10-31 | 1981-05-14 | Basf Ag, 6700 Ludwigshafen | Iron corrosion inhibition - with aq. system contg. alkanolamine salt(s) of alkenyl succinic acid(s) |
US4282007A (en) * | 1980-09-22 | 1981-08-04 | Texaco Inc. | Novel fuel composition containing alcohol |
US4283296A (en) * | 1978-08-21 | 1981-08-11 | Texaco Inc. | Amine salt of N-triazolyl-hydrocarbyl succinamic acid and lubricating oil composition containing same |
US4917809A (en) * | 1986-11-11 | 1990-04-17 | Ciba-Geigy Corporation | High-temperature lubricants |
WO1990007563A1 (en) * | 1988-12-29 | 1990-07-12 | Mobil Oil Corporation | Reaction products of polyalkenyl succinimides, aldehydes, and triazoles and lubricant and fuel compositions containing same |
US4963278A (en) * | 1988-12-29 | 1990-10-16 | Mobil Oil Corporation | Lubricant and fuel compositions containing reaction products of polyalkenyl succinimides, aldehydes, and triazoles |
US4981493A (en) * | 1989-01-27 | 1991-01-01 | Texaco Inc. | ORI-Inhibited and deposit-resistant motor fuel composition |
US4997456A (en) * | 1989-09-11 | 1991-03-05 | Ethyl Petroleum Additives, Inc. | Fuel compositions |
US5030370A (en) * | 1990-03-08 | 1991-07-09 | Exxon Chemical Patents Inc. | Novel dispersant viscosity index improver compositions |
US5122616A (en) * | 1989-09-11 | 1992-06-16 | Ethyl Petroleum Additives, Inc. | Succinimides |
US5194167A (en) * | 1991-05-08 | 1993-03-16 | Mobil Oil Corporation | Quaternary ammonium salts of mercaptothiadiazoles and related heterocyclic derivatives as antioxidant and antiwear additives |
US5211865A (en) * | 1990-03-08 | 1993-05-18 | Exxon Chemical Patents Inc. | Multifunctional viscosity index improver-dispersant antioxidant |
US5232615A (en) * | 1990-03-08 | 1993-08-03 | Exxon Chemical Patents Inc. | Heterocyclic nitrogen compound Mannich base derivatives of polyolefin-substituted amines for oleaginous compositions |
US5271856A (en) * | 1990-03-08 | 1993-12-21 | Exxon Chemical Patents Inc. | Heterocyclic nitrogen compound Mannich base derivatives of amino-substituted polymers for oleaginous compositions |
US5273671A (en) * | 1990-03-08 | 1993-12-28 | Exxon Chemical Patents Inc. | Multifunctional viscosity index improver-dispersant antioxidant |
US6468946B2 (en) | 1998-07-06 | 2002-10-22 | The Lubrizol Corporation | Mixed phosphorus compounds and lubricants containing the same |
US20090093384A1 (en) * | 2007-10-03 | 2009-04-09 | The Lubrizol Corporation | Lubricants That Decrease Micropitting for Industrial Gears |
CN102533404A (en) * | 2011-07-11 | 2012-07-04 | 布兰诺工业包装材料(上海)有限公司 | Efficient lubrication type anti-rust oil and preparation method thereof |
US9481841B2 (en) | 2004-12-09 | 2016-11-01 | The Lubrizol Corporation | Process of preparation of an additive and its use |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2475570B1 (en) * | 1980-02-08 | 1986-04-11 | Lubrizol Corp | BENZOTRIAZOLE COMPOSITIONS DISPERSABLE IN LUBRICANT COMPOUNDS AND METHODS FOR THEIR PREPARATION |
FR2485031A1 (en) * | 1980-03-10 | 1981-12-24 | Lubrizol Corp | SULFURATED BENZOTRIAZOLE-OLEFIN COMPOSITIONS AND LUBRICANTS AND CONCENTRATES CONTAINING THEM |
GB9505232D0 (en) * | 1995-03-15 | 1995-05-03 | Castrol Ltd | Anti-microbial compositions |
GB9505183D0 (en) * | 1995-03-15 | 1995-05-03 | Castrol Ltd | Anti-microbial compositions |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3256187A (en) * | 1963-05-17 | 1966-06-14 | Socony Mobil Oil Co Inc | Cutting fluid |
-
1973
- 1973-10-04 US US403692A patent/US3897351A/en not_active Expired - Lifetime
-
1974
- 1974-09-26 GB GB4192574A patent/GB1465981A/en not_active Expired
- 1974-09-27 CA CA210,260A patent/CA1039293A/en not_active Expired
- 1974-09-27 JP JP49110686A patent/JPS5065509A/ja active Pending
- 1974-09-30 ZA ZA00746217A patent/ZA746217B/en unknown
- 1974-10-02 IT IT28037/74A patent/IT1033101B/en active
- 1974-10-03 FR FR7433390A patent/FR2246551B1/fr not_active Expired
- 1974-10-03 NL NLAANVRAGE7413095,A patent/NL175431C/en not_active IP Right Cessation
- 1974-10-04 DE DE19742447550 patent/DE2447550A1/en not_active Withdrawn
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US3256187A (en) * | 1963-05-17 | 1966-06-14 | Socony Mobil Oil Co Inc | Cutting fluid |
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4107060A (en) * | 1975-06-17 | 1978-08-15 | Mobil Oil Corporation | Lubricant compositions containing biocidal, antirust additives |
US4255214A (en) * | 1977-11-21 | 1981-03-10 | Falconer Plate Glass Corporation | Methods of manufacturing and protecting mirrors |
US4153563A (en) * | 1978-05-24 | 1979-05-08 | Mobil Oil Corporation | Lubricant compositions containing benzotriazole-allyl sulfide reaction products |
US4283296A (en) * | 1978-08-21 | 1981-08-11 | Texaco Inc. | Amine salt of N-triazolyl-hydrocarbyl succinamic acid and lubricating oil composition containing same |
US4212754A (en) * | 1979-04-23 | 1980-07-15 | Mobil Oil Corporation | Chelate detergent and antiwear additive for lubricants derived from hydroxyalkylated benzotriazoles |
DE2943963A1 (en) * | 1979-10-31 | 1981-05-14 | Basf Ag, 6700 Ludwigshafen | Iron corrosion inhibition - with aq. system contg. alkanolamine salt(s) of alkenyl succinic acid(s) |
US4282007A (en) * | 1980-09-22 | 1981-08-04 | Texaco Inc. | Novel fuel composition containing alcohol |
US4917809A (en) * | 1986-11-11 | 1990-04-17 | Ciba-Geigy Corporation | High-temperature lubricants |
WO1990007563A1 (en) * | 1988-12-29 | 1990-07-12 | Mobil Oil Corporation | Reaction products of polyalkenyl succinimides, aldehydes, and triazoles and lubricant and fuel compositions containing same |
US4963278A (en) * | 1988-12-29 | 1990-10-16 | Mobil Oil Corporation | Lubricant and fuel compositions containing reaction products of polyalkenyl succinimides, aldehydes, and triazoles |
US4981493A (en) * | 1989-01-27 | 1991-01-01 | Texaco Inc. | ORI-Inhibited and deposit-resistant motor fuel composition |
US5122616A (en) * | 1989-09-11 | 1992-06-16 | Ethyl Petroleum Additives, Inc. | Succinimides |
US4997456A (en) * | 1989-09-11 | 1991-03-05 | Ethyl Petroleum Additives, Inc. | Fuel compositions |
US5030370A (en) * | 1990-03-08 | 1991-07-09 | Exxon Chemical Patents Inc. | Novel dispersant viscosity index improver compositions |
US5211865A (en) * | 1990-03-08 | 1993-05-18 | Exxon Chemical Patents Inc. | Multifunctional viscosity index improver-dispersant antioxidant |
US5232615A (en) * | 1990-03-08 | 1993-08-03 | Exxon Chemical Patents Inc. | Heterocyclic nitrogen compound Mannich base derivatives of polyolefin-substituted amines for oleaginous compositions |
US5271856A (en) * | 1990-03-08 | 1993-12-21 | Exxon Chemical Patents Inc. | Heterocyclic nitrogen compound Mannich base derivatives of amino-substituted polymers for oleaginous compositions |
US5273671A (en) * | 1990-03-08 | 1993-12-28 | Exxon Chemical Patents Inc. | Multifunctional viscosity index improver-dispersant antioxidant |
US5376152A (en) * | 1990-03-08 | 1994-12-27 | Exxon Chemical Patents Inc. | Heterocyclic nitrogen compound mannich base derivatives of polyolefin-substituted amines for oleaginous compositions |
US5194167A (en) * | 1991-05-08 | 1993-03-16 | Mobil Oil Corporation | Quaternary ammonium salts of mercaptothiadiazoles and related heterocyclic derivatives as antioxidant and antiwear additives |
US6468946B2 (en) | 1998-07-06 | 2002-10-22 | The Lubrizol Corporation | Mixed phosphorus compounds and lubricants containing the same |
US9481841B2 (en) | 2004-12-09 | 2016-11-01 | The Lubrizol Corporation | Process of preparation of an additive and its use |
US20090093384A1 (en) * | 2007-10-03 | 2009-04-09 | The Lubrizol Corporation | Lubricants That Decrease Micropitting for Industrial Gears |
CN102533404A (en) * | 2011-07-11 | 2012-07-04 | 布兰诺工业包装材料(上海)有限公司 | Efficient lubrication type anti-rust oil and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
FR2246551B1 (en) | 1979-03-16 |
ZA746217B (en) | 1976-05-26 |
IT1033101B (en) | 1979-07-10 |
NL175431C (en) | 1984-11-01 |
GB1465981A (en) | 1977-03-02 |
NL175431B (en) | 1984-06-01 |
JPS5065509A (en) | 1975-06-03 |
CA1039293A (en) | 1978-09-26 |
NL7413095A (en) | 1975-04-08 |
AU7404474A (en) | 1976-04-08 |
DE2447550A1 (en) | 1975-04-17 |
FR2246551A1 (en) | 1975-05-02 |
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