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Publication numberUS3245908 A
Publication typeGrant
Publication dateApr 12, 1966
Filing dateNov 18, 1963
Priority dateNov 18, 1963
Publication numberUS 3245908 A, US 3245908A, US-A-3245908, US3245908 A, US3245908A
InventorsLowe Warren
Original AssigneeChevron Res
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Lubricant composition
US 3245908 A
Abstract  available in
Images(2)
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Claims  available in
Description  (OCR text may contain errors)

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,

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US1854898 *Sep 11, 1930Apr 19, 1932Gulf Production CompanyMethod of protecting an immersed surface from corrosive action
US2194478 *Aug 2, 1937Mar 26, 1940Shell DevExtreme pressure lubricant
US2366074 *May 26, 1942Dec 26, 1944Standard Oil Dev CoCorrosion resistant composition
US2434978 *Apr 15, 1944Jan 27, 1948Hayward R BakerAnticorrosion additives for synthetic lubricants
US2715108 *May 6, 1952Aug 9, 1955Shell DevLubricating compositions
US2776917 *Jul 10, 1956Jan 8, 1957Gillette CoArticle with corrosion-inhibited surface and composition for coating said surface
US2809160 *Dec 29, 1955Oct 8, 1957California Research CorpLubricant composition
US2991251 *Sep 27, 1957Jul 4, 1961Exxon Research Engineering CoCorrosion inhibiting lubricating composition
FR1254094A * Title not available
GB612775A * Title not available
GB815050A * Title not available
GB922831A * Title not available
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3506463 *Jan 4, 1967Apr 14, 1970Mobil Oil CorpMold release agent
US3666662 *Apr 23, 1970May 30, 1972Chevron ResAlkali metal succinamate compositions for lubricating oils
US4107054 *Jun 27, 1977Aug 15, 1978Continental Oil CompanyNatural or synthetic lubricant - alkenylsuccinimide dispersant - anthranilic acid, alkylbenzoic acid, or alkylcatechol as rust inhibitor
US5498809 *May 22, 1995Mar 12, 1996Exxon Chemical Patents Inc.Terminal ethylvinylidene groups which can be functionalized, dispersants
US5554310 *Jun 9, 1994Sep 10, 1996Exxon Chemical Patents Inc.Trisubstituted unsaturated polymers
US5629434 *Sep 25, 1995May 13, 1997Exxon Chemical Patents IncReaction product of polymer with at least one ethylenic double bond with carbon monoxide and nucleophilic trapping agent; dispersants, viscosity modifiers
US5643859 *Jun 17, 1994Jul 1, 1997Exxon Chemical Patents Inc.Fuel dispersant
US5646332 *Jun 17, 1994Jul 8, 1997Exxon Chemical Patents Inc.Batch Koch carbonylation process
US5650536 *Jun 17, 1994Jul 22, 1997Exxon Chemical Patents Inc.Continuous process for production of functionalized olefins
US5663130 *Mar 11, 1996Sep 2, 1997Exxon Chemical Patents IncPolymers derived from ethylene and 1-butene for use in the preparation of lubricant dispersant additives
US5696064 *Aug 23, 1995Dec 9, 1997Exxon Chemical Patents Inc.From carbon monoxide and a nucleophilic trapping agent
US5698722 *Jun 6, 1995Dec 16, 1997Exxon Chemical Patents Inc.Blend of addition polymer, carbon monoxide and nucleophilic trapping agent
US5703256 *Dec 16, 1996Dec 30, 1997Exxon Chemical Patents Inc.Functionalization of polymers based on Koch chemistry and derivatives thereof
US5717039 *Jun 6, 1995Feb 10, 1998Exxon Chemical Patents Inc.Functionalization of polymers based on Koch chemistry and derivatives thereof
US5767046 *May 15, 1997Jun 16, 1998Exxon Chemical CompanyPrepared by reacting an olefin, carbon monoxide, an acid catalyst and a nucleophilic trapping agent selected from hydroxy- and thiol-containing compounds
US6030930 *May 14, 1997Feb 29, 2000Exxon Chemical Patents IncUseful in lubricating oils, and to concentrates containing the oil-soluble dispersant additives