US3857791A - Lubricating oil additive and lubricating oil compositions containing same - Google Patents
Lubricating oil additive and lubricating oil compositions containing same Download PDFInfo
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- US3857791A US3857791A US00257043A US25704372A US3857791A US 3857791 A US3857791 A US 3857791A US 00257043 A US00257043 A US 00257043A US 25704372 A US25704372 A US 25704372A US 3857791 A US3857791 A US 3857791A
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- lubricating oil
- additive
- amine
- amido
- alkylenepolyamine
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Classifications
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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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
-
- 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
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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
- C10M2215/08—Amides
-
- 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
- C10M2215/08—Amides
- C10M2215/082—Amides containing hydroxyl groups; Alkoxylated derivatives
-
- 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
- C10M2215/26—Amines
-
- 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
-
- 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
-
- 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
- C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
-
- 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
- C10N2040/26—Two-strokes or two-cycle engines
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B75/00—Other engines
- F02B75/02—Engines characterised by their cycles, e.g. six-stroke
- F02B2075/022—Engines characterised by their cycles, e.g. six-stroke having less than six strokes per cycle
- F02B2075/025—Engines characterised by their cycles, e.g. six-stroke having less than six strokes per cycle two
Definitions
- ABSTRACT An improved lubricating oil additive having, among other desirable properties, detergency and superior rust inhibitory characteristics and lubricating oil compositions containing said additive.
- the additive is a two component mixture comprising a high molecular weight amide-amine and a high molecular weight bydrocarbylamine.
- the preferred lubricating oil composition is a two-cycle engine oil composition comprising a major proportion of a hydrocarbon lubricating oil and a minor proportion of the two component additive of the invention.
- Hydrocarbon lubricating oil compositions commonly have a number of desirable properties imparted thereto by the incorporation of additives.
- the principal properties imparted by the use of additives are improved detergency, anti-wear properties, and enhanced rust inhibiting characteristics. It is often required that separate detergency, anti-wear, and rust inhibiting additives be employed.
- the aggregate additive level often approaches a point where a number of undesirable results occur.
- the detergency additive, the anti-wear additive and the rust inhibitor may be incompatible and interact to form a precipitate in the lubricating oil composition.
- the combined additives may also contribute to such deficiencies as storage instability where the additives flocculate when the lubricating oil composition is allowed to stand for a period of time, or poor water tolerance where in lubricating oil composition containing the additives forms emulsions or becomes turbid when contacted with water.
- the two-cycle engine oil may not be readily miscible with gasoline.
- this invention consists of a lubricating oil additive comprising a mixture of a high molecular weight amide-amine and a hydrocarbylamine having a molecular weight in the range of about 425-10,000; and a hydrocarbon lubricating oil composition comprising a major proportion of a hydrocarbon lubricating oil and a minor proportion of the foregoing additive mixture.
- a lubricating oil detergency, anti-wear, and antirust additive and hydrocarbon lubricating oil composition containing said additive which are characterized by excellent detergency, good wear characteristics, and rust inhibitory properties.
- the hydrocarbon lubricating oil compositions of this invention have such desirable properties as good storage stability, good water tolerance, and, in the case oftwo-cycle engine oil compositions, good gasoline miscibility.
- amido-amines are known detergency additives for lubricating oil compositions and, in addition, often have good anti-wear properties.
- lubricating oil compositions containing such amido-amines do not have satisfactory anti-rust properties in the absence of a rust inhibitor. At times, even the addition of appreciable amounts of rust inhibitor do not impart sufficiently satisfactory anti-rust properties.
- an economical and superior lubricating oil detergency and anti-wear additive having unexpected rust inhibiting properties may be prepared by mixing a high molecular weight amidoamine and a hydrocarbylamine having a molecular weight in the range of about 425-l0,000.
- the anti-rust characteristics of our additive mixture are surprising since neither the amido-amine alone nor the hydrocarbylamine alone has appreciable rust inhibiting properties.
- lubricating oil compositions containing our additive mixture and no other rust inhibitor often have anti-rust properties that are superior to those of lubricating oil compositions containing a high molecular weight amido-amine at the same concentration as our addiitive plus a rust inhibitor.
- the high molecular weight amido-amine component of our additive mixture is the condensation product of an alkylenepolyamine and less than the stoichiometric amount ofa fatty monocarboxylic acid such that the resultant amido-amine has about 1-3 amino groups in addition to the amide groups.
- the fatty monocarboxylic acid moiety is aliphatic and contains about 12-30 carbons and preferably contains about 14-20 carbons.
- the fatty monocarboxylic acid may be either straight chain or branched chain, but mixtures of straight chain and branched chain acids are preferred.
- Suitable fatty monocarboxylic acids are dodecanoic acid, eicosanoic acid, elaidic acid, triacontanoic acid, stearic acid, isosteric acid, ricinoleic acid, pentadecanoic acid, and alpha-ethyldodecanoic acid.
- Preferred are mixtures of straight and branched chain fatty monocarboxylic acids containing about 14-20 carbons.
- the alkylenepolyamine moiety of the amide-amine broadly contains about 2-8 amino groups and preferably about 3-6 amino groups.
- the alkylenepolyamine may broadly contain about 2-16, and preferably about 4-12, carbons.
- suitable alkylenepolyamines are ethylenediamine, propylenediamine, diethylenetriamine, hexamethylenediamine, triethylenetetramine, tetraethylenepentamine, and pentaethylenehexamine.
- the preferred alkylenepolyamine is tetraethylenepentamine.
- the amide-amine component of our additive mixture is prepared by condensing the alkylenepolyamine with less than the stoichiometric amount of the fatty monocarboxylic acid so that the resultant amido-amine contains about 1-3 amino groups in addition to the amide groups. It is therefore apparent that, from a consideration of the number of amino groups in the alkylenepolyamine, one skilled in the art could readily determine the mole ratio of polyamine to be condensed with fatty monocarboxylic acid to obtain the desired amido-amine. Broadly, however, the mole ratio of alkylenepolyamine to monocarboxylic acid is from about 1:1 to about 1:7 and preferably from about 1:1 to about 1:5.
- amido-amine is the condensation product of one mole of tetraethylenepentamine and about three moles of a mixture of branched and straight chained fatty moncarboxylic acids containing about 14-20 carbons.
- Such an amidoamine is manufactured by the Oronite Additives Division of Chevron Chemical Company and marketed under the designation Oronite 340-D.
- the hydrocarbylamine component of our additive mixture is broadly a high molecular weight branched chain aliphatic hydrocarbon monoamine or an alkylenepolyamine having a molecular weight in the range of about 425l0,000 and preferably in the range of about 450-5,000, as well as mixtures of said monoamine and said alkylenepolyamine. Preferred, however, are high molecular weight alkylenepolyamines.
- the alkylenepolyamines contain about 2-8, and preferably about 2-6 amino nitrogens.
- the high molecular weight branched chain aliphatic hydrocarbon monoamine has the empirical formula R-NHA wherein A is either hydrogen or lower alkyl, preferably of from 1 to about 3 carbons, and R is a branched chain aliphatic hydrocarbon substantially free of olefinic unsaturation and of from about 420-1500 average molecular weight.
- Suitable branched chain aliphatic hydrocarbon monoamines are polypropenylamine, polyisobutenylamine, N-polyisobutenyl dimethylamine, N-polyisobutenyl methylethylamine, N-polypropenyl diethylamine, N- polyisobutenyl N-methylaniline, N-polyisobutenyl morpholine, N-polyisobutenyl piperidine, and N-poly(lbutene) propylamine.
- alkylenepolyamines are high molecular weight alkylenepolyamines.
- alkylenepolyamines.having the empirical formula suitable alkylenepolyamines are N,N'- di(polypropenyl) diethylenetriamine; N,N'- di(polyisobutenyl) diethylenetriamine; N,N'- di(polyisobutenyl) triethylenetetramine; N,N'- di(polypropenyl) tetraethylenepentamine; N ,N
- Oronite OGA-472 manufactured by the Oronite Additives Division of Chevron Chemical Company.
- Oronite OGA-472 is an approximately 70 volume percent solution of the alkylenepolyamine in a mixed aromatic hydrocarbonaliphatic alcohol solvent.
- the lubricating oil additives of this invention comprise a mixture of the foregoing amide-amine and hydrocarbylamine wherein the volume ratio of said amide-amine to said hydrocarbylamine is from about 1:10 to about :1 and preferably from about 1:3 to about 3:1.
- the most preferred lubricating oil additive has an approximately 1:07 volume ratio of amidoamine to hydrocarbylamine.
- the lubricating oil compositions of this invention 1 compositions comprising a major proportion of a hydrocarbon lubricating oil and about 4-12 volume percent of the additive mixture.
- the lubricating oil compositions of this invention may also contain minor amounts of conventional materials such as dyes, alcohols, viscosity index improvers, antioxidants, and light petroleum hydrocarbon fractions.
- the lubricating oil compositions of this invention have general utility as' such, but their use as two-cycle engine oils is particularly advantageous.
- the efficacy ofthe additive mixture of this invention and of lubricating oil compositions containing said additive mixture regarding dete'rgency and rust inhibitory properties was determined by means of engine tests and the Boating Industry Association (BIA) rust test.
- BIA rust test selected steel panels which have been matched with regard to surface and edge finish are thoroughly cleaned with cold naphtha and then by dipping in boiling naphtha followed by dipping in boiling anhydrous methanol. The panel, at F, is dipped in the lubricating oil composition to be tested, which is at 70F, for 10 minutes and is then drained vertically in 70F still air for 10 minutes.
- the panel is immersed vertically into a 70i 10F salt water solution having a composition of one-half pound of chemically pure sodium chloride in 1 gallon of distilled water. To pass the test, the panel should show no visible rust after the test period except for the area within one-eighth inch of the panel edges or within one-eighth inch of any holes.
- a lubricating oil additive is prepared from equal volumes of the amido-amine designated Oronite 340-D and the 70 volume percent alkylenepolyamine solution designated Oronite OGA-472.
- a hydrocarbon lubricating oil composition is prepared comprising a major proportion of a hydrocarbon lubricating oil and 8.4 volume percent of the foregoing additive mixture.
- a gasoline composition is prepared having a 50:1 fuelzoil ratio wherein the gasoline contains 0.5 ml. of tetraethyl lead per gallon and wherein the oil is the lubricating oil composition containing 8.4 volume percent of the instant additive mixture.
- EXAMPLE 11 A number of two-cycle engine oil compositions are prepared containing the two component additive mixture of this invention.
- the amido-amine component of the additive is Oronite 340-D and the hydrocarbylamine component is an alkylenepolyamine solution, namely, Oronite OGA-472.
- a similar two-cycle engine oil composition is prepared containing only the amido-amine component Oronite 340-D.
- the lubricating oil compositions contain minor amounts of conventional materials such as long chain fatty alcohol; Stoddard Solvent, a well known light petroleum fraction; and, in all but one composition, a separate anti-rust additive.
- the two-cycle engine oil compositions are then subjected to the BIA rust test for various periods of time and thereafter evaluated as pass or fail.
- the makeups of the two-cycle engine oil compositions and the results of the BIA rust tests are shown in Table l.
- said lubricating oil composition have good storage stability and water tolerance.
- twocycle engine oil compositions containing the additive mixture of this invention exhibit ready solubility in gasoline.
- This invention therefore provides a lubricating oil additive mixture that imparts to hydrocarbon lubricating oil compositions, and particularly to twocycle engine oil compositions, a number of desirable properties.
- Luricating oil compositions containing the two component additive of this invention thus have good detergency and anti-wear characteristics and, unexpectedly, excellent rust inhibitory properties.
- the lubricating oil compositions also exhibit good storage stability and water tolerance characteristics.
- a lubricating oil additive comprising a mixture of an amido-amine and a hydrocarbylamine, in which a. the amido-amine/hydrocarbylamine volume ratio varies from about 1/10 to about 10/1,
- the amido-amine is the condensation product of an alkylenepolyamine containing about 2-6 amino nitrogens and 2-16 carbon atoms and less than the stoichiometric amount of a fatty monocarboxylic acid containing about 14-20 carbon atoms, the mole ratio of said alkylenepolyamine to said fatty monocarboxylic acid being from about 1:1 to about 1:5, and
- the hydrocarbylamine has a molecular weight from about 450 to about 5000 and is selected from the group consisting of branched chaim aliphatic hydrocarbon monoamines and alkylenepolyamines, and wherein the alkylenepolyamine has the empirical formula Rti: (I-IC1I -C1I- -1 I-] wherein R a branched chain aliphatic hydrocarbon selected from the group consisting of polypropylene and polyisobutylene and having an average molecular weight ranging from about 450 to about 1500,
- amido-amine is the condensation product of 1 mole of 5 tetraethylenepentamine and about 3 moles ofa mixture of branched and straight chain fatty monocarboxylic acids containing about 14-20 carbons.
- the lubricating oil additive of claim 1 wherein the volume ratio of said amido-amine to said alkylenepolyamine is from about 1:3 to about 3:1.
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Abstract
An improved lubricating oil additive having, among other desirable properties, detergency and superior rust inhibitory characteristics and lubricating oil compositions containing said additive. The additive is a two component mixture comprising a high molecular weight amido-amine and a high molecular weight hydrocarbylamine. The preferred lubricating oil composition is a two-cycle engine oil composition comprising a major proportion of a hydrocarbon lubricating oil and a minor proportion of the two component additive of the invention.
Description
United States Patent [191 Marcellis et al.
[451 Dec. 31, 1974 LUBRICATING OIL ADDITIVE AND LUBRICATING OIL COMPOSITIONS CONTAINING SAME Inventors: Alphonso W. Marcellis, Boonton;
Donald H. Peterson, Parlin, both of NJ.
Cities Service Oil Company, Tulsa, Okla.
Filed: May 25, 1972 Appl. No.: 257,043
Assignee:
US. Cl. 252/515 A, 44/58 Int. Cl Cl0m 1/32 Field of Search 252/515 A; 44/58 References Cited UNITED STATES PATENTS l/ 1960 Lindstrom et al. 44/58 X 2/1965 Benoit 252/515 A X 3,275,554 9/1966 Wagenaar 252/50 3,310,492 3/1967 Benoit 3,585,137 6/1971 Bosniack et al. 252/515 A Primary ExaminerPatrick P. Garvin Assistant ExaminerAndrew H. Metz Attorney, Agent, or Firm.1ohn W. Carpenter 5 7] ABSTRACT An improved lubricating oil additive having, among other desirable properties, detergency and superior rust inhibitory characteristics and lubricating oil compositions containing said additive. The additive is a two component mixture comprising a high molecular weight amide-amine and a high molecular weight bydrocarbylamine. The preferred lubricating oil composition is a two-cycle engine oil composition comprising a major proportion of a hydrocarbon lubricating oil and a minor proportion of the two component additive of the invention.
7 Claims, N0 Drawings LUBRICATING OIL ADDITIVE AND LUBRICATING OIL COMPOSITIONS CONTAINING SAME BACKGROUND OF THE INVENTION Hydrocarbon lubricating oil compositions commonly have a number of desirable properties imparted thereto by the incorporation of additives. The principal properties imparted by the use of additives are improved detergency, anti-wear properties, and enhanced rust inhibiting characteristics. It is often required that separate detergency, anti-wear, and rust inhibiting additives be employed. Thus, in order to improve detergency, anti-wear, and rust inhibitory properties, the aggregate additive level often approaches a point where a number of undesirable results occur. For example, the detergency additive, the anti-wear additive and the rust inhibitor may be incompatible and interact to form a precipitate in the lubricating oil composition. The combined additives may also contribute to such deficiencies as storage instability where the additives flocculate when the lubricating oil composition is allowed to stand for a period of time, or poor water tolerance where in lubricating oil composition containing the additives forms emulsions or becomes turbid when contacted with water. Furthermore, in the special case of twocycle engine oils which are mixed with the gasoline fuel, there is the added possibility that the two-cycle engine oil may not be readily miscible with gasoline.
SUMMARY OF THE INVENTION It is therefore an object of this invention to provide an economical lubricating oil additive having detergency, anti-wear, and rust inhibiting properties.
It is another object of this invention to provide 3 oil compositions having enchanced detergency, anti-wear, and rust inhibiting properties.
It is yet another object of this invention to provide lubricating oil compositions having storage stability and good water tolerance.
It is a particular object of this invention to provide two-cycle engine oil compositions having detergency, anti-wear, and rust inhibiting properties as wellas good storage stability, water tolerance, and ready miscibility with gasoline.
Yet other objects and advantages will be apparent to those skilled in the art from the following description.
The foregoing objects are achieved in accordance with the practice of this invention. Broadly, this invention consists of a lubricating oil additive comprising a mixture of a high molecular weight amide-amine and a hydrocarbylamine having a molecular weight in the range of about 425-10,000; and a hydrocarbon lubricating oil composition comprising a major proportion of a hydrocarbon lubricating oil and a minor proportion of the foregoing additive mixture.
Thus, by the practice of this invention, there are provided a lubricating oil detergency, anti-wear, and antirust additive and hydrocarbon lubricating oil composition containing said additive which are characterized by excellent detergency, good wear characteristics, and rust inhibitory properties. In addition, the hydrocarbon lubricating oil compositions of this invention have such desirable properties as good storage stability, good water tolerance, and, in the case oftwo-cycle engine oil compositions, good gasoline miscibility.
DETAILED DESCRIPTION High molecular weight amido-amines are known detergency additives for lubricating oil compositions and, in addition, often have good anti-wear properties. However, lubricating oil compositions containing such amido-amines do not have satisfactory anti-rust properties in the absence ofa rust inhibitor. At times, even the addition of appreciable amounts of rust inhibitor do not impart sufficiently satisfactory anti-rust properties.
We have now discovered that an economical and superior lubricating oil detergency and anti-wear additive having unexpected rust inhibiting properties may be prepared by mixing a high molecular weight amidoamine and a hydrocarbylamine having a molecular weight in the range of about 425-l0,000. The anti-rust characteristics of our additive mixture are surprising since neither the amido-amine alone nor the hydrocarbylamine alone has appreciable rust inhibiting properties. In fact, lubricating oil compositions containing our additive mixture and no other rust inhibitor often have anti-rust properties that are superior to those of lubricating oil compositions containing a high molecular weight amido-amine at the same concentration as our addiitive plus a rust inhibitor.
Broadly, the high molecular weight amido-amine component of our additive mixture is the condensation product of an alkylenepolyamine and less than the stoichiometric amount ofa fatty monocarboxylic acid such that the resultant amido-amine has about 1-3 amino groups in addition to the amide groups. The fatty monocarboxylic acid moiety is aliphatic and contains about 12-30 carbons and preferably contains about 14-20 carbons. The fatty monocarboxylic acid may be either straight chain or branched chain, but mixtures of straight chain and branched chain acids are preferred. Examples of suitable fatty monocarboxylic acids are dodecanoic acid, eicosanoic acid, elaidic acid, triacontanoic acid, stearic acid, isosteric acid, ricinoleic acid, pentadecanoic acid, and alpha-ethyldodecanoic acid. Preferred are mixtures of straight and branched chain fatty monocarboxylic acids containing about 14-20 carbons.
The alkylenepolyamine moiety of the amide-amine broadly contains about 2-8 amino groups and preferably about 3-6 amino groups. The alkylenepolyamine may broadly contain about 2-16, and preferably about 4-12, carbons. Examples of suitable alkylenepolyamines are ethylenediamine, propylenediamine, diethylenetriamine, hexamethylenediamine, triethylenetetramine, tetraethylenepentamine, and pentaethylenehexamine. The preferred alkylenepolyamine is tetraethylenepentamine.
As set forth above, the amide-amine component of our additive mixture is prepared by condensing the alkylenepolyamine with less than the stoichiometric amount of the fatty monocarboxylic acid so that the resultant amido-amine contains about 1-3 amino groups in addition to the amide groups. It is therefore apparent that, from a consideration of the number of amino groups in the alkylenepolyamine, one skilled in the art could readily determine the mole ratio of polyamine to be condensed with fatty monocarboxylic acid to obtain the desired amido-amine. Broadly, however, the mole ratio of alkylenepolyamine to monocarboxylic acid is from about 1:1 to about 1:7 and preferably from about 1:1 to about 1:5. The most preferred amido-amine is the condensation product of one mole of tetraethylenepentamine and about three moles of a mixture of branched and straight chained fatty moncarboxylic acids containing about 14-20 carbons. Such an amidoamine is manufactured by the Oronite Additives Division of Chevron Chemical Company and marketed under the designation Oronite 340-D.
The hydrocarbylamine component of our additive mixture is broadly a high molecular weight branched chain aliphatic hydrocarbon monoamine or an alkylenepolyamine having a molecular weight in the range of about 425l0,000 and preferably in the range of about 450-5,000, as well as mixtures of said monoamine and said alkylenepolyamine. Preferred, however, are high molecular weight alkylenepolyamines. The alkylenepolyamines contain about 2-8, and preferably about 2-6 amino nitrogens.
The high molecular weight branched chain aliphatic hydrocarbon monoamine has the empirical formula R-NHA wherein A is either hydrogen or lower alkyl, preferably of from 1 to about 3 carbons, and R is a branched chain aliphatic hydrocarbon substantially free of olefinic unsaturation and of from about 420-1500 average molecular weight. Examples of suitable branched chain aliphatic hydrocarbon monoamines are polypropenylamine, polyisobutenylamine, N-polyisobutenyl dimethylamine, N-polyisobutenyl methylethylamine, N-polypropenyl diethylamine, N- polyisobutenyl N-methylaniline, N-polyisobutenyl morpholine, N-polyisobutenyl piperidine, and N-poly(lbutene) propylamine.
The preferred hydrocarbylamines, as stated above, are high molecular weight alkylenepolyamines. Most preferred are alkylenepolyamines.having the empirical formula suitable alkylenepolyamines are N,N'- di(polypropenyl) diethylenetriamine; N,N'- di(polyisobutenyl) diethylenetriamine; N,N'- di(polyisobutenyl) triethylenetetramine; N,N'- di(polypropenyl) tetraethylenepentamine; N ,N
di(polyisobutenyl) tetraethylenepentamine, N,N',N"- tri(polyisobutenyl)tetraethylenepentamine; N,N-di(poly-l-butenyl) triethylenetetramine; and N,N'-di(polyisobutenyl) di(trimethylene) triamine. A particularly suitable alkylenepolyamine meeting the above requirements is Oronite OGA-472 manufactured by the Oronite Additives Division of Chevron Chemical Company. Oronite OGA-472 is an approximately 70 volume percent solution of the alkylenepolyamine in a mixed aromatic hydrocarbonaliphatic alcohol solvent.
The lubricating oil additives of this invention comprise a mixture of the foregoing amide-amine and hydrocarbylamine wherein the volume ratio of said amide-amine to said hydrocarbylamine is from about 1:10 to about :1 and preferably from about 1:3 to about 3:1. The most preferred lubricating oil additive has an approximately 1:07 volume ratio of amidoamine to hydrocarbylamine.
The lubricating oil compositions of this invention 1 compositions comprising a major proportion of a hydrocarbon lubricating oil and about 4-12 volume percent of the additive mixture. The lubricating oil compositions of this invention may also contain minor amounts of conventional materials such as dyes, alcohols, viscosity index improvers, antioxidants, and light petroleum hydrocarbon fractions. The lubricating oil compositions of this invention have general utility as' such, but their use as two-cycle engine oils is particularly advantageous.
The efficacy ofthe additive mixture of this invention and of lubricating oil compositions containing said additive mixture regarding dete'rgency and rust inhibitory properties was determined by means of engine tests and the Boating Industry Association (BIA) rust test. In the BIA rust test, selected steel panels which have been matched with regard to surface and edge finish are thoroughly cleaned with cold naphtha and then by dipping in boiling naphtha followed by dipping in boiling anhydrous methanol. The panel, at F, is dipped in the lubricating oil composition to be tested, which is at 70F, for 10 minutes and is then drained vertically in 70F still air for 10 minutes. The panel is immersed vertically into a 70i 10F salt water solution having a composition of one-half pound of chemically pure sodium chloride in 1 gallon of distilled water. To pass the test, the panel should show no visible rust after the test period except for the area within one-eighth inch of the panel edges or within one-eighth inch of any holes.
The following specific examples will serve to further illustrate the instant invention.
EXAMPLE I A lubricating oil additive is prepared from equal volumes of the amido-amine designated Oronite 340-D and the 70 volume percent alkylenepolyamine solution designated Oronite OGA-472. A hydrocarbon lubricating oil composition is prepared comprising a major proportion of a hydrocarbon lubricating oil and 8.4 volume percent of the foregoing additive mixture. A gasoline composition is prepared having a 50:1 fuelzoil ratio wherein the gasoline contains 0.5 ml. of tetraethyl lead per gallon and wherein the oil is the lubricating oil composition containing 8.4 volume percent of the instant additive mixture. An air cooled two-cycle engine is operated on the gasoline composition for a l00-hour period after which time the engine is dismantled and rated for cleanliness and wear. The piston cleanliness is rated 8 on a scale of l-lO wherein a 10 rating is perfect. Crankase cleanliness is rated as clean. Engine wear is negligible. It is apparent from the foregoing that the lubricating oil additive of the instant invention is an effective detergency and anti-wear additive.
EXAMPLE 11 A number of two-cycle engine oil compositions are prepared containing the two component additive mixture of this invention. The amido-amine component of the additive is Oronite 340-D and the hydrocarbylamine component is an alkylenepolyamine solution, namely, Oronite OGA-472. For comparison, a similar two-cycle engine oil composition is prepared containing only the amido-amine component Oronite 340-D. The lubricating oil compositions contain minor amounts of conventional materials such as long chain fatty alcohol; Stoddard Solvent, a well known light petroleum fraction; and, in all but one composition, a separate anti-rust additive. The two-cycle engine oil compositions are then subjected to the BIA rust test for various periods of time and thereafter evaluated as pass or fail. The makeups of the two-cycle engine oil compositions and the results of the BIA rust tests are shown in Table l.
"711 volume percent solution of alkylenepolyamine.
The data in Table I show that prior art two-cycle engine oil compositon 1 containing only the amido-amine detergency additive plus a separate rust inhibitor fails the rust test after 24 hours. In contrast, two-cycle engine oil compositions 2, 3, and 4 containing the two component additive mixture of the instant invention pass the rust test after 71 hours if a separate anti-rust additive is present and pass the rust test after 24 hours if no separate anti-rust additive is present. It is therefore apparcut that the instant two component lubricating oil additive has unexpectedly superior rust inhibiting properties than does the amide-amine component alone plus a separate rust inhibitor.
EXAMPLE 111 TABLE 11 Hydrocarbon Oil. vol. 71.5 71.5 7 Oronite 340-D, vol. 7: 8.4 Oronite 0GA-472," vol.
Long Chain Fatty Alcohol,
vol. Stoddard Solvent, vol. lsopropyl Alcohol. vol. 7r
Mui
w a lIILII- N NLII TABLE ll-Continued BlA Rust Test: 7
8 Hours Fail Fail Pass 24 Hours Fail Fail Pass 71) volumc perccnl solution of alkylenepolyamine.
From Table 11 it is seen that two-cycle engine oil compositions 5 and 6 containing the individual components of the instant additive fail the BIA rust test after 8 and 24 hours. Engine oil composition 7, containing an essentially equivalent amount of the two component additive of our invention, passes the BIA rust test after 8 hours and 24 hours. The data therefore illustrate the unexpected rust inhibiting properties, absent from the individual amido-amine and alkylenepolyamine components, that are present when the two components are combined.
In addition to excellent detergency and anti-wear properties and the unexpected rust inhibiting characteristics of lubricating oil compositions of this invention, said lubricating oil composition have good storage stability and water tolerance. In addition, twocycle engine oil compositions containing the additive mixture of this invention exhibit ready solubility in gasoline. This invention therefore provides a lubricating oil additive mixture that imparts to hydrocarbon lubricating oil compositions, and particularly to twocycle engine oil compositions, a number of desirable properties. Luricating oil compositions containing the two component additive of this invention thus have good detergency and anti-wear characteristics and, unexpectedly, excellent rust inhibitory properties. The lubricating oil compositions also exhibit good storage stability and water tolerance characteristics.
While this invention has been illustrated by the presentation of specific examples, it will be understood that the scope of the invention is limited only by the appended claims. I
We claim:
1. A lubricating oil additive comprising a mixture of an amido-amine and a hydrocarbylamine, in which a. the amido-amine/hydrocarbylamine volume ratio varies from about 1/10 to about 10/1,
b. the amido-amine is the condensation product of an alkylenepolyamine containing about 2-6 amino nitrogens and 2-16 carbon atoms and less than the stoichiometric amount of a fatty monocarboxylic acid containing about 14-20 carbon atoms, the mole ratio of said alkylenepolyamine to said fatty monocarboxylic acid being from about 1:1 to about 1:5, and
c. the hydrocarbylamine has a molecular weight from about 450 to about 5000 and is selected from the group consisting of branched chaim aliphatic hydrocarbon monoamines and alkylenepolyamines, and wherein the alkylenepolyamine has the empirical formula Rti: (I-IC1I -C1I- -1 I-] wherein R a branched chain aliphatic hydrocarbon selected from the group consisting of polypropylene and polyisobutylene and having an average molecular weight ranging from about 450 to about 1500,
a an integer having the value of l or 2, b an integer having the value of from 1 to about 5. 2. The lubricating oil additive of claim 1 wherein the amido-amine is the condensation product of 1 mole of 5 tetraethylenepentamine and about 3 moles ofa mixture of branched and straight chain fatty monocarboxylic acids containing about 14-20 carbons.
3. The lubricating oil additive of claim 1 wherein the volume ratio of said amido-amine to said alkylenepolyamine is from about 1:3 to about 3:1.
4. The lubricating oil additive of claim 2 wherein the volume ratio of said amide-amine to said alabout 4-12 volume percent of the additive of claim 4. l l l
Claims (7)
1. A LUBRICATING OIL ADDITIVE COMPRISING A MIXTURE OF AN AMIDO-AMINE AND A HYDROCARBYLAMINE IN WHICH, A. THE AMIDO-AMINE/HYDROCARBYLAMINE VOLUME RATIO VARIES FROM ABOUT 1/10 TO ABOUT 10/1, B. THE AMIDO-AMINE IS THE CONDENSATION PRODUCT OF AN ALKYLENEPOLYAMINE CONTAINING ABOUT 2-6 AMINO NITROGENS AND 2-16 CARBON ATOMS AND LESS THAN THE STOICHIOMETRIC AMOUNT OF A FATTY MONOCARBOXYLIC CONTAINING ABOUT 14-20 CARBON ATOMS, THE MOLE RATIO OF SAID ALKYLENEPOLYAMINE TO SAID FATTY MONOCARBOXYLIC ACID BEINF FROM ABOUT 1:1 TO ABOUT 1:5, AND C. THE HYDROCARBYLAMINE HAS A MOLECULAR WEIGHT FROM ABOUT 450 TO ABOUT 5000 AND IS SELECTED FROM THE GROUP CONSISTING OF BRANCHED CHAIM ALIPHATIC HYDROCARBON MONOAMINES AND ALKYLENEPOLYAMINES, AND WHEREIN THE ALKYLENEPOLYAMINE HAS THE EMPIRICAL FORMULA FFIG-01 WHEREIN R'' = A BRANCHED CHAIN ALIPHATIC HYDROCARBONS SELECTED FROM THE GROUP CONSISTING OF POLYPROPYLENE AND POLYISOBUTYLENE AND HAVING AN AVERAGE MOLECULAR WEIGHT RANGING FROM ABOUT 450 TO ABOUT 15000 A = AN INTEGER HAVING THE VALUE OF 1 OR 2, B = AN INTEGER HAVING THE VALUE OF FROM 1 TO ABOUT 5.
2. The lubricating oil additive of claim 1 wherein the amido-amine is the condensation product of 1 mole of tetraethylenepentamine and about 3 moles of a mixture of branched and straight chain fatty monocarboxylic acids containing about 14-20 carbons.
3. The lubricating oil additive of claim 1 wherein the volume ratio of said amido-amine to said alkylenepolyamine is from about 1:3 to about 3:1.
4. The lubricating oil additive of claim 2 wherein the volume ratio of said amido-amine to said alkylenepolyamine is about 1: 0.7.
5. A hydrocarbon lubricating oil composition comprising a major proportion of a hydrocarbon lubricating oil and about 1-30 volume percent of the additive of claim 1.
6. A hydrocarbon lubricating oil composition comprising a major proportion of a hydrocarbon lubricating oil and about 2-20 volume percent of the additive of claim 3.
7. A two-cycle engine oil composition comprising a major proportion of a hydrocarbon lubricating oil and about 4-12 volume percent of the additive of claim 4.
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US00257043A US3857791A (en) | 1972-05-25 | 1972-05-25 | Lubricating oil additive and lubricating oil compositions containing same |
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US00257043A US3857791A (en) | 1972-05-25 | 1972-05-25 | Lubricating oil additive and lubricating oil compositions containing same |
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Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4152342A (en) * | 1975-07-21 | 1979-05-01 | The Dow Chemical Company | Oleophilic amidopolyethylenepolyamines |
US5178782A (en) * | 1985-03-12 | 1993-01-12 | The Lubrizol Corporation | Metal salts of mixed aromatic/aliphatic phosphorodithioic acids |
WO1993003120A1 (en) * | 1991-08-09 | 1993-02-18 | The Lubrizol Corporation | Two-cycle lubricants and methods of using the same |
US5395539A (en) * | 1988-10-24 | 1995-03-07 | Exxon Chemical Patents Inc. | Amide containing friction modifier for use in power transmission fluids |
US5498353A (en) * | 1994-11-22 | 1996-03-12 | Chinese Petroleum Corp. | Semi-synthetic two-stroke engine oil formulation |
US5569407A (en) * | 1994-03-25 | 1996-10-29 | Mobil Oil Corporation | Additives for fuels and lubricants |
US5672573A (en) * | 1996-04-10 | 1997-09-30 | Exxon Chemical Patents Inc. | Amicloamine derivatives of carboxylic and thiocarboxylic-functionalized hydrocarbon polymers |
US5773393A (en) * | 1991-09-16 | 1998-06-30 | The Lubrizol Corporation | Oil compositions useful in hydraulic fluids |
US5814111A (en) * | 1995-03-14 | 1998-09-29 | Shell Oil Company | Gasoline compositions |
US6242394B1 (en) | 1991-05-30 | 2001-06-05 | The Lubrizol Corporation | Two-stroke cycle lubricant and method of using same |
WO2010005947A2 (en) | 2008-07-11 | 2010-01-14 | Innospec Fuel Specialties, LLC | Fuel composition with enhanced low temperature properties |
US20100186853A1 (en) * | 2007-07-27 | 2010-07-29 | Idemitsu Kosan Co., Ltd. | Heat-treatment oil composition |
US20100258070A1 (en) * | 2007-09-27 | 2010-10-14 | Innospec Limited | Fuel compositions |
US20100293844A1 (en) * | 2007-09-27 | 2010-11-25 | Macmillan John Alexander | Additives for Diesel Engines |
US20100299992A1 (en) * | 2007-09-27 | 2010-12-02 | Jacqueline Reid | Fuel compositions |
WO2010136822A2 (en) | 2009-05-29 | 2010-12-02 | Innospec Limited | Method and use |
WO2010139994A1 (en) | 2009-06-01 | 2010-12-09 | Innospec Limited | Improvements in efficiency |
EP2302020A1 (en) | 2007-07-28 | 2011-03-30 | Innospec Limited | Use of additives for improving oxidation stability of a fuel oil composition |
WO2011110860A1 (en) | 2010-03-10 | 2011-09-15 | Innospec Limited | Fuel composition comprising detergent and quaternary ammonium salt additive |
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US9243199B2 (en) | 2007-09-27 | 2016-01-26 | Innospec Limited | Fuel compositions |
US9315752B2 (en) | 2007-09-27 | 2016-04-19 | Innospec Limited | Fuel compositions |
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US11186791B2 (en) | 2017-03-30 | 2021-11-30 | Innospec Limited | Composition, method and use |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2922708A (en) * | 1958-02-26 | 1960-01-26 | California Research Corp | Gasoline compositions |
US3169980A (en) * | 1961-03-31 | 1965-02-16 | California Research Corp | Fatty acid polyamide |
US3275554A (en) * | 1963-08-02 | 1966-09-27 | Shell Oil Co | Polyolefin substituted polyamines and lubricants containing them |
US3310492A (en) * | 1964-09-08 | 1967-03-21 | Chevron Res | Oils for two-cycle engines containing basic amino-containing detergents and aryl halides |
US3585137A (en) * | 1969-06-25 | 1971-06-15 | Exxon Research Engineering Co | Synthetic ester lubricating oil composition |
-
1972
- 1972-05-25 US US00257043A patent/US3857791A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2922708A (en) * | 1958-02-26 | 1960-01-26 | California Research Corp | Gasoline compositions |
US3169980A (en) * | 1961-03-31 | 1965-02-16 | California Research Corp | Fatty acid polyamide |
US3275554A (en) * | 1963-08-02 | 1966-09-27 | Shell Oil Co | Polyolefin substituted polyamines and lubricants containing them |
US3310492A (en) * | 1964-09-08 | 1967-03-21 | Chevron Res | Oils for two-cycle engines containing basic amino-containing detergents and aryl halides |
US3585137A (en) * | 1969-06-25 | 1971-06-15 | Exxon Research Engineering Co | Synthetic ester lubricating oil composition |
Cited By (38)
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US4152342A (en) * | 1975-07-21 | 1979-05-01 | The Dow Chemical Company | Oleophilic amidopolyethylenepolyamines |
US5178782A (en) * | 1985-03-12 | 1993-01-12 | The Lubrizol Corporation | Metal salts of mixed aromatic/aliphatic phosphorodithioic acids |
US5395539A (en) * | 1988-10-24 | 1995-03-07 | Exxon Chemical Patents Inc. | Amide containing friction modifier for use in power transmission fluids |
US5484543A (en) * | 1988-10-24 | 1996-01-16 | Exxon Chemical Patents Inc. | Amide containing friction modifier for use in power transmission fluids |
US6242394B1 (en) | 1991-05-30 | 2001-06-05 | The Lubrizol Corporation | Two-stroke cycle lubricant and method of using same |
WO1993003120A1 (en) * | 1991-08-09 | 1993-02-18 | The Lubrizol Corporation | Two-cycle lubricants and methods of using the same |
US5264005A (en) * | 1991-08-09 | 1993-11-23 | The Lubrizol Corporation | Two-cycle lubricants and methods of using the same |
US5773393A (en) * | 1991-09-16 | 1998-06-30 | The Lubrizol Corporation | Oil compositions useful in hydraulic fluids |
US5569407A (en) * | 1994-03-25 | 1996-10-29 | Mobil Oil Corporation | Additives for fuels and lubricants |
US5498353A (en) * | 1994-11-22 | 1996-03-12 | Chinese Petroleum Corp. | Semi-synthetic two-stroke engine oil formulation |
US5814111A (en) * | 1995-03-14 | 1998-09-29 | Shell Oil Company | Gasoline compositions |
US5672573A (en) * | 1996-04-10 | 1997-09-30 | Exxon Chemical Patents Inc. | Amicloamine derivatives of carboxylic and thiocarboxylic-functionalized hydrocarbon polymers |
US20100186853A1 (en) * | 2007-07-27 | 2010-07-29 | Idemitsu Kosan Co., Ltd. | Heat-treatment oil composition |
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US9034060B2 (en) | 2007-09-27 | 2015-05-19 | Innospec Fuel Specialties Llc | Additives for diesel engines |
US20100299992A1 (en) * | 2007-09-27 | 2010-12-02 | Jacqueline Reid | Fuel compositions |
US9315752B2 (en) | 2007-09-27 | 2016-04-19 | Innospec Limited | Fuel compositions |
US9243199B2 (en) | 2007-09-27 | 2016-01-26 | Innospec Limited | Fuel compositions |
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US9157041B2 (en) | 2007-09-27 | 2015-10-13 | Innospec Limited | Fuel compositions |
US20100293844A1 (en) * | 2007-09-27 | 2010-11-25 | Macmillan John Alexander | Additives for Diesel Engines |
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US9085740B2 (en) | 2009-02-25 | 2015-07-21 | Innospec Limited | Methods relating to fuel compositions |
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US9493720B2 (en) | 2010-05-10 | 2016-11-15 | Innospec Limited | Gasoline composition, method and use |
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