US3245908A - Lubricant composition - Google Patents
Lubricant composition Download PDFInfo
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- US3245908A US3245908A US324177A US32417763A US3245908A US 3245908 A US3245908 A US 3245908A US 324177 A US324177 A US 324177A US 32417763 A US32417763 A US 32417763A US 3245908 A US3245908 A US 3245908A
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- lubricant composition
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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
- 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
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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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
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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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/024—Propene
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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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
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- 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
- C10M2207/14—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
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- C—CHEMISTRY; METALLURGY
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- 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
- C10M2207/14—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/142—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings polycarboxylic
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- 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
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C—CHEMISTRY; METALLURGY
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- 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
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- 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
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- 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
- C10M2215/08—Amides
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- 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
- C10M2215/08—Amides
- C10M2215/082—Amides containing hydroxyl groups; Alkoxylated derivatives
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- C—CHEMISTRY; METALLURGY
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- 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
- C10M2215/26—Amines
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/28—Amides; Imides
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/044—Polyamides
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/045—Polyureas; Polyurethanes
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/046—Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
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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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- 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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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/251—Alcohol fueled engines
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
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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
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
- C10N2040/28—Rotary engines
Definitions
- This invention relates to novel lubricating compositions. More particularly, it relates to lubricant comp0- sitions having superior non-corrosive and non-deposit forming properties.
- Lubricating oils under normal operating conditions, generally undergo oxidative deterioration resulting in the production of substances highly corrosive to metal parts of modern engine and like machinery. Particularly susceptible to such corrosion are the alloy metal (usually copper-lead) bearings employed in todays internal combustion engines.
- phthalic acids especially isophthalic and terephthalic acids as corrosion inhibiting components of lubricant compositions
- These compounds represent highly effective corrosion inhibitors possessing many desirable characteristics such as the ability to be used in combination with numerous classes of both lubricating oil bases and lubricant additives of various types.
- a decrease in detergent activity often results.
- their use results in an increase in the amount of varnish and other carbonaceous deposits deposited upon piston valves and skirts and in piston ring grooves. These deposits are deleterious to engine operation and their elimination is a highly desirable objective evidenced by numerous advances recently made in producing better detergent type additives.
- a new and superior lubrieating composition having excellent non-corrosive and non-deposit forming characteristics can be prepared from a major proportion of an oil of lubricating viscosity in combination with a high molecular weight nitrogen-containing detergent type additive, said combination being corrosive to metal surfaces in normal use, and a minor portion sufiicient to inhibit corrosion of 2,2'-biphenyl dicarboxylic acid.
- novel lubricating compositions of this invention are characterized by remarkable corrosion inhibiting properties over extended operational periods and by greatly improved lubricating of bearings and other sliding surfaces.
- An outstanding advantage of the particular inhibitor lies in the fact that its addition results in no increase in the deposit-forrning characteristics of the compositions, a result common with the inhibitors of the prior art.
- of particular advantage is the ability of these compositions to provide superior lubrication for particular bearings such as silver-containing bearings Without the usually concommitant tendency to form underhead deposits in such heavy duty diesel service.
- the corrosion inhibiting characteristics of 2,2'-biphenyldicarboxylic acid are obtained in particular in combination with recently developed nitrogen-containing nonmetallic ashless detergents in lubricating oil compositions.
- detergents are those derived from alkenyl succinic anhydrides having 30 or more carbon atoms in the alkenyl group and amine compounds, such as tetraethylene pentarnine, N-aminoethyl piperazine, dimethylaminopropylamine, etc.
- the detergent additive is obtained by heating an alkenyl succinic anhydride with at least 0.5 mole of an amine.
- the substituted succinic anhydrides contemplated as reactants in the process can be readily obtained by heating maleic anhydride with a high molecular weight olefin or with a chlorinated high molecular weight olefin at a temperature from about to 200 C.
- Typical high molecular weight olefins which can be employed are polyethylene, polypropylene, polyisobutylene, etc. Polyisobutylene is preferred.
- Suitable polyamine reactants are ethylenediamine, diethylene triamine, tetraethylene pentamine, and the like. Tetraethylene pentamine is a preferred polyamine reactant.
- a preferred embodiment of the detergent additive is the product obtained by heating one mole of a polyisobutenyl succinic anhydride having about 65 carbon atoms in the olefin chain with 0.9 mole of tetraethylene pentamine.
- the detergent additive is employed in the lubricant composition in an amount suflicient to impart detergency. Generally, amounts from 0.1 to 10% by weight are preferred.
- the additives are a class of chemical compounds recognized in the art as possessing the ability to enable a lubricating oil medium to maintain oxidation products, resins, and other insoluble material in suspension or disprobably due to the removal of naturally formed protective films from bearings and other sliding surfaces.
- a compatible and efficient corrosion inhibitor with these types of compounds is especially desirable.
- the corrosion inhibitor of this invention is employed in an amount sulficient to inhibit corrosion. In general, amounts up to about 1.0% by Weight are suflicient. A preferred range for most lubricant compositions is from about 0.01% to about 0.5% by weight.
- any of the Well-known types of lubricating oils can be used as the base oils for the compositions of this invention. These oils are corrosive to metal surfaces under normal operating conditions.
- base oils are naphthenic base, parafiin base, and mixed base mineral oils; synthetic oils, for example, alkylene polymers, such as polymers of propylene, butylene, etc., and mixtures thereof; alkylene oxide type polymers; dicarboxylic acid esters; phosphorous esters; silicon esters such as si1icates and polysiloxanes; and alkyl aromatic hydrocarbons.
- the corrosion inhibitor of EXAMPLE I 0.15% by weight of 2,2'-biphenyldicarboxylic acid was added to a lubricating composition comprising 3.0% by weight of a polybutenyl succinimide detergent type additive in a lubricating oil base which was a solvent refined paraffinic neutral oil of SAE 30 grade.
- the detergent was prepared by heating 1 mole of polybutenyl succinic anhydride having about 65 carbon atoms in the alkenyl chain with 0.9 mole of tetraethylene pentamine.
- the lubricant composition prepared in Example I was subjected to the L-4 Engine Test and compared with a simple of base oil containing the same detergent and with a sample containing 0.15% by weight of terephthalic acid as a corrosion inhibitor.
- the corrosion characteristics of a lubricant composition is determined in a Chevrolet standard 6-cy1inder engine. Weighed copper-lead test bearings and new piston rings are installed. The test is run at a constant engine speed at about 3000 rpm. under a load of 30 brake horsepower for a period of 36 hours after a runin period of 8 hours. The outlet temperature of the jacket coolant is about 200 F. and the oil sump temperature about 280 F. At the conclusion of the test the engine is disassembled and the pistons are removed and inspected for varnish deposits and rated for cleanliness on a basis of to 10, 10 being perfectly clean. The bearings are weighed to determine total weight loss due to corrosion. Table I describes the results of tests performed comparing the additive of this invention with terephthalic acid.
- 2,2'biphenyldicarboxylic acid compares favorably with terephthalic acid in its ability to reduce bearing corrosion with this type of lubricant composition.
- its great superiority lies in the fact that it does not contribute to lowering the varnish rating of the engine as does the terephthalic acid.
- 2,2-biphenyldicarboxylic acid provides excellent corrosion inhibition under actual engine operation and aids in maintaining extremely high engine cleanliness ratings.
- the L4 Engine Test is more iully described in the CRC Handbook, 1946 edition, Coordinating Research Council, New York, New York.
- a lubricant composition comprising a major portion of an oil of lubricating viscosity in combination with a minor portion of an alkenyl succinimide lubricating oil detergent sufficient to impart detergency, said combination being corrosive to metal surfaces in normal use and a minor portion sufficient to inhibit corrosion, of 2,2biphenyldicarboxyiic acid.
Description
United States Patent 3,245,908 LUBRICANT COMPOSITION Warren Lowe, Berkeley, Calif., assignor to Chevron Research Company, a corporation of Delaware No Drawing. Filed Nov. 18, 1963, Ser. No. 324,177 3 Claims. (Cl. 25251.5)
This invention relates to novel lubricating compositions. More particularly, it relates to lubricant comp0- sitions having superior non-corrosive and non-deposit forming properties.
Lubricating oils, under normal operating conditions, generally undergo oxidative deterioration resulting in the production of substances highly corrosive to metal parts of modern engine and like machinery. Particularly susceptible to such corrosion are the alloy metal (usually copper-lead) bearings employed in todays internal combustion engines.
Therefore it is necessary to add to the lubricating oils, substances which act to reduce the corrosive effect upon the metal surfaces. Corrosion inhibitors which have been employed in the past have not been completely satisfactory. A number of additives have been employed that were not highly effective, thus allowing corrosion of the parts sought to be protected. Others, while quite effective initially, are used up rapidly in service and lose their effectiveness.
Another problem of many prior art anticorrodents has been the fact that they could not be combined successfully in compositions with additives commonly used to eifect wear inhibition, sludge inhibitors, pour point depression, detergency, etc. Thus, a desirable inhibitor may be combined with these types of additives without adversely affecting the properties of either the anticorrodent or the other additive.
Furthermore, many known corrosion inhibitors contain active sulfur and are thus undesirable for use with bearings containing silver and similar metals. The use of silver-containing bearings has greatly increased in such classes of engines as marine and locomotive diesels. Thus, non-sulfur-containing lubricants possessing anticorrodent properties are especially desirable.
The use of phthalic acids, especially isophthalic and terephthalic acids as corrosion inhibiting components of lubricant compositions is described in Stewart et al. US. Patent 2,809,160. These compounds represent highly effective corrosion inhibitors possessing many desirable characteristics such as the ability to be used in combination with numerous classes of both lubricating oil bases and lubricant additives of various types. However, in some applications, when these compounds are combined in lubricating compositions with certain nitrogen-containing detergents, while excellent anticorrodent properties are displayed, a decrease in detergent activity often results. Thus their use results in an increase in the amount of varnish and other carbonaceous deposits deposited upon piston valves and skirts and in piston ring grooves. These deposits are deleterious to engine operation and their elimination is a highly desirable objective evidenced by numerous advances recently made in producing better detergent type additives.
It has now been found that a new and superior lubrieating composition having excellent non-corrosive and non-deposit forming characteristics can be prepared from a major proportion of an oil of lubricating viscosity in combination with a high molecular weight nitrogen-containing detergent type additive, said combination being corrosive to metal surfaces in normal use, and a minor portion sufiicient to inhibit corrosion of 2,2'-biphenyl dicarboxylic acid.
The novel lubricating compositions of this invention are characterized by remarkable corrosion inhibiting properties over extended operational periods and by greatly improved lubricating of bearings and other sliding surfaces. An outstanding advantage of the particular inhibitor lies in the fact that its addition results in no increase in the deposit-forrning characteristics of the compositions, a result common with the inhibitors of the prior art. As noted above, of particular advantage is the ability of these compositions to provide superior lubrication for particular bearings such as silver-containing bearings Without the usually concommitant tendency to form underhead deposits in such heavy duty diesel service.
The corrosion inhibiting characteristics of 2,2'-biphenyldicarboxylic acid are obtained in particular in combination with recently developed nitrogen-containing nonmetallic ashless detergents in lubricating oil compositions. Examples of such detergents are those derived from alkenyl succinic anhydrides having 30 or more carbon atoms in the alkenyl group and amine compounds, such as tetraethylene pentarnine, N-aminoethyl piperazine, dimethylaminopropylamine, etc.
The detergent additive is obtained by heating an alkenyl succinic anhydride with at least 0.5 mole of an amine.
The substituted succinic anhydrides contemplated as reactants in the process can be readily obtained by heating maleic anhydride with a high molecular weight olefin or with a chlorinated high molecular weight olefin at a temperature from about to 200 C. Typical high molecular weight olefins which can be employed are polyethylene, polypropylene, polyisobutylene, etc. Polyisobutylene is preferred.
Examples of suitable polyamine reactants are ethylenediamine, diethylene triamine, tetraethylene pentamine, and the like. Tetraethylene pentamine is a preferred polyamine reactant.
A preferred embodiment of the detergent additive is the product obtained by heating one mole of a polyisobutenyl succinic anhydride having about 65 carbon atoms in the olefin chain with 0.9 mole of tetraethylene pentamine.
The detergent additive is employed in the lubricant composition in an amount suflicient to impart detergency. Generally, amounts from 0.1 to 10% by weight are preferred.
The additives are a class of chemical compounds recognized in the art as possessing the ability to enable a lubricating oil medium to maintain oxidation products, resins, and other insoluble material in suspension or disprobably due to the removal of naturally formed protective films from bearings and other sliding surfaces. Thus the use of a compatible and efficient corrosion inhibitor with these types of compounds is especially desirable.
The corrosion inhibitor of this invention is employed in an amount sulficient to inhibit corrosion. In general, amounts up to about 1.0% by Weight are suflicient. A preferred range for most lubricant compositions is from about 0.01% to about 0.5% by weight.
Any of the Well-known types of lubricating oils can be used as the base oils for the compositions of this invention. These oils are corrosive to metal surfaces under normal operating conditions. Examples of such base oils are naphthenic base, parafiin base, and mixed base mineral oils; synthetic oils, for example, alkylene polymers, such as polymers of propylene, butylene, etc., and mixtures thereof; alkylene oxide type polymers; dicarboxylic acid esters; phosphorous esters; silicon esters such as si1icates and polysiloxanes; and alkyl aromatic hydrocarbons.
As previously mentioned, the corrosion inhibitor of EXAMPLE I 0.15% by weight of 2,2'-biphenyldicarboxylic acid was added to a lubricating composition comprising 3.0% by weight of a polybutenyl succinimide detergent type additive in a lubricating oil base which was a solvent refined paraffinic neutral oil of SAE 30 grade. The detergent was prepared by heating 1 mole of polybutenyl succinic anhydride having about 65 carbon atoms in the alkenyl chain with 0.9 mole of tetraethylene pentamine.
In order to demonstrate the effectiveness of 2,2'-biphenyldicarboxylic acid as a non-deposit forming anticorrodent, the lubricant composition prepared in Example I was subjected to the L-4 Engine Test and compared with a simple of base oil containing the same detergent and with a sample containing 0.15% by weight of terephthalic acid as a corrosion inhibitor.
In the L-4 test, the corrosion characteristics of a lubricant composition is determined in a Chevrolet standard 6-cy1inder engine. Weighed copper-lead test bearings and new piston rings are installed. The test is run at a constant engine speed at about 3000 rpm. under a load of 30 brake horsepower for a period of 36 hours after a runin period of 8 hours. The outlet temperature of the jacket coolant is about 200 F. and the oil sump temperature about 280 F. At the conclusion of the test the engine is disassembled and the pistons are removed and inspected for varnish deposits and rated for cleanliness on a basis of to 10, 10 being perfectly clean. The bearings are weighed to determine total weight loss due to corrosion. Table I describes the results of tests performed comparing the additive of this invention with terephthalic acid.
Table I As shown by the above data, 2,2'biphenyldicarboxylic acid compares favorably with terephthalic acid in its ability to reduce bearing corrosion with this type of lubricant composition. However, its great superiority lies in the fact that it does not contribute to lowering the varnish rating of the engine as does the terephthalic acid. Thus 2,2-biphenyldicarboxylic acid provides excellent corrosion inhibition under actual engine operation and aids in maintaining extremely high engine cleanliness ratings.
The L4 Engine Test is more iully described in the CRC Handbook, 1946 edition, Coordinating Research Council, New York, New York.
I claim:
1. A lubricant composition comprising a major portion of an oil of lubricating viscosity in combination with a minor portion of an alkenyl succinimide lubricating oil detergent sufficient to impart detergency, said combination being corrosive to metal surfaces in normal use and a minor portion sufficient to inhibit corrosion, of 2,2biphenyldicarboxyiic acid.
2. The lubricant composition of claim 1 wherein the oil of lubricating viscosity is a mineral lubricating oil.
3. The lubricant composition of claim 1 wherein the detergent additive is a polybutenyl succinimide prepared from a polybutenyl succinic anhydride having about carbon atoms in the alkenyl chain and tetraalkylene pentamine, said detergent additive being present in an amount of from 0.1% to 10% by weight.
References Cited by the Examiner DANIEL E. WYMAN, Primary Examiner.
P. P. GARVIN, Examiner,
Claims (1)
1. A LUBRICANT COMPOSITION COMPRISING A MAJOR PORTION OF AN OIL LUBRICATING VISCOSITY IN COMBINATION WITH A MINOR PORTION OF AN ALKENYL SUCCINIMIDE LUBRICATING OIL DETERGENT SUFFICIENT TO IMPART DETERGENCY, SAID COMBINATION BEING CORROSIVE TO METAL SURFACES IN NORMAL USE AND A MINOR PORTION SUFFICIENT TO INHIBIT CORROSION, OF 2,2''BIPHENYLDICARBOXYLIC ACID.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US324177A US3245908A (en) | 1963-11-18 | 1963-11-18 | Lubricant composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US324177A US3245908A (en) | 1963-11-18 | 1963-11-18 | Lubricant composition |
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US3245908A true US3245908A (en) | 1966-04-12 |
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US324177A Expired - Lifetime US3245908A (en) | 1963-11-18 | 1963-11-18 | Lubricant composition |
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Cited By (10)
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US3506463A (en) * | 1967-01-04 | 1970-04-14 | Mobil Oil Corp | Mold release agent |
US3666662A (en) * | 1970-04-23 | 1972-05-30 | Chevron Res | Alkali metal succinamate compositions for lubricating oils |
US4107054A (en) * | 1977-06-27 | 1978-08-15 | Continental Oil Company | Lubricating oil compositions |
US5498809A (en) * | 1992-12-17 | 1996-03-12 | Exxon Chemical Patents Inc. | Polymers derived from ethylene and 1-butene for use in the preparation of lubricant dispersant additives |
US5554310A (en) * | 1992-12-17 | 1996-09-10 | Exxon Chemical Patents Inc. | Trisubstituted unsaturated polymers |
US5629434A (en) * | 1992-12-17 | 1997-05-13 | Exxon Chemical Patents Inc | Functionalization of polymers based on Koch chemistry and derivatives thereof |
US5643859A (en) * | 1992-12-17 | 1997-07-01 | Exxon Chemical Patents Inc. | Derivatives of polyamines with one primary amine and secondary of tertiary amines |
US5646332A (en) * | 1992-12-17 | 1997-07-08 | Exxon Chemical Patents Inc. | Batch Koch carbonylation process |
US5650536A (en) * | 1992-12-17 | 1997-07-22 | Exxon Chemical Patents Inc. | Continuous process for production of functionalized olefins |
US5767046A (en) * | 1994-06-17 | 1998-06-16 | Exxon Chemical Company | Functionalized additives useful in two-cycle engines |
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Publication number | Priority date | Publication date | Assignee | Title |
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US3506463A (en) * | 1967-01-04 | 1970-04-14 | Mobil Oil Corp | Mold release agent |
US3666662A (en) * | 1970-04-23 | 1972-05-30 | Chevron Res | Alkali metal succinamate compositions for lubricating oils |
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US5554310A (en) * | 1992-12-17 | 1996-09-10 | Exxon Chemical Patents Inc. | Trisubstituted unsaturated polymers |
US5629434A (en) * | 1992-12-17 | 1997-05-13 | Exxon Chemical Patents Inc | Functionalization of polymers based on Koch chemistry and derivatives thereof |
US5643859A (en) * | 1992-12-17 | 1997-07-01 | Exxon Chemical Patents Inc. | Derivatives of polyamines with one primary amine and secondary of tertiary amines |
US5646332A (en) * | 1992-12-17 | 1997-07-08 | Exxon Chemical Patents Inc. | Batch Koch carbonylation process |
US5498809A (en) * | 1992-12-17 | 1996-03-12 | Exxon Chemical Patents Inc. | Polymers derived from ethylene and 1-butene for use in the preparation of lubricant dispersant additives |
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US5698722A (en) * | 1992-12-17 | 1997-12-16 | Exxon Chemical Patents Inc. | Functionalization of polymers based on Koch chemistry and derivatives thereof |
US5703256A (en) * | 1992-12-17 | 1997-12-30 | Exxon Chemical Patents Inc. | Functionalization of polymers based on Koch chemistry and derivatives thereof |
US5717039A (en) * | 1992-12-17 | 1998-02-10 | Exxon Chemical Patents Inc. | Functionalization of polymers based on Koch chemistry and derivatives thereof |
US6030930A (en) * | 1992-12-17 | 2000-02-29 | Exxon Chemical Patents Inc | Polymers derived from ethylene and 1-butene for use in the preparation of lubricant disperant additives |
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