US3711406A - Lubricating oil containing an hydroxylated amine and an overbased sulfonate or phenate - Google Patents
Lubricating oil containing an hydroxylated amine and an overbased sulfonate or phenate Download PDFInfo
- Publication number
- US3711406A US3711406A US00045567A US3711406DA US3711406A US 3711406 A US3711406 A US 3711406A US 00045567 A US00045567 A US 00045567A US 3711406D A US3711406D A US 3711406DA US 3711406 A US3711406 A US 3711406A
- Authority
- US
- United States
- Prior art keywords
- oil
- carbon atoms
- amine
- phenate
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/062—Oxides; Hydroxides; Carbonates or bicarbonates
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/024—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/027—Neutral salts thereof
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/028—Overbased salts thereof
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- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
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- C10M2209/106—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing four carbon atoms only
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- C10M2209/107—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106
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- C10M2209/109—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
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- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/11—Complex polyesters
- C10M2209/111—Complex polyesters having dicarboxylic acid centres
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- 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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- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/062—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups bound to the aromatic ring
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- C10M2215/064—Di- and triaryl amines
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- C10M2219/046—Overbasedsulfonic acid salts
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- C10M2223/045—Metal containing thio derivatives
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- C10M2223/047—Thioderivatives not containing metallic elements
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- C10M2223/065—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds containing sulfur
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
Definitions
- Lubricating oils are employed not only for lubrication, but as a vehicle to promote a wide variety of protection for the surfaces lubricated by the oil.
- the tendency for rusting has required that lubricating oils include additives which inhibit rust.
- bases capable of neutralizing the acids which are formed during fuel combustion, and by blow-by or other mechanisms which are introduced into the oil.
- SUMMARY Poly(hydroxyalkylated) alkyl-substituted amines in combination with alkaline earth metal carbonates dispersed in a hydrocarbon lubricating oil medium are combined to provide rust protection, corrosion protection and acid neutralization.
- the carbonate will be present in the oil to provide an alkalinity value of at least 0.5 mg. KOH/ g. while the amine will be present in at least 0.05 weight percent.
- compositions of this invention are a combination of a hydroxyalkylated alkyl-substituted amine and an alkaline earth metal carbonate in a hydrocarbon oil of lubricating viscosity.
- the composition provides enhanced rust and corrosion protection.
- Other additives may also be included to fulfill functions other than those provided for by the base and hydroxyalkylated amine, as Well as to augment the functions of the aforementioned additives.
- the hydroxyalkylated amines will be present in at least 0.05 weight percent and not greater than about 3 weight percent in compositions in use in internal combustion engines. More usually, the hydroxyalkylated amine will be present in from about 0.1 to 2 Weight percent and preferably from about 0.2 to 1 Weight percent.
- the alkaline earth metal carbonate will normally be present to provide alkalinity values of from about 0.5 to mg. KOH/g, more usually from about 1 to 20 mg. KOH/g., (for method of determination, see Abbott & Farley, Methods and Significance of Base Determination in Marine Cylinder Lubrication Oils, 23rd ASLE Meeting, May, 1968). While alkalinity values in excess of 10 mg. KOH/ g. are not essential to rusting protection, values in excess of 10 mg. KOH/ g. will frequently be used for a particular service. In marine lubrication, alkalinity values are high, while in automobile lubrication, alkylinity values are relatively low.
- additives will be present in varying amounts, the total amount or" other additives normally not exceeding 15 weight percent and usually not being less than 0.1 weight percent.
- additives include ashless dispersants such as succinimides, hydrocarbyl alkylene polyamines, etc., dithiophosphates, carboxylic acid corrsion inhibitors, etc.
- a is 0 or 1
- U is alkylene of from 2 to 3 carbon atoms, preferably 2 carbon atoms, there being at least 2 carbon atoms between nitrogen and oxygen;
- Y is alkylene of from 2 to 3 carbon atoms, preferably 3 carbon atoms, there being at least 2 carbon atoms between the nitrogen atoms;
- R is an aliphatic hydrocarbon group of from 12 to 24 carbon atoms, either straight chain or branched chain, preferably straight chain, having from 0 to 2 sites of aliphatic unsaturation, usually ethylenic, preferably 0 to 1 site of ethylenic unsaturation.
- R may be a single alkyl group or a mixture of alkyl groups substantially all of the alkyl groups falling within the specified carbon range.
- R is alkyl or alkenyl of from 16 to 18 carbon atoms and particularly preferred 18 carbon atoms.
- the R groups may be derived from synthetic or natural sources.
- Illustrative alkyl groups are derived from tallow amines, oleyl amine, stearyl amine, lauryl amine, behenyl amine, etc.
- Illustrative compounds which fined use within the scope of this invention are N,N,N'-tri(Z-hydroxyethyl) N-octadecyl propylene diamine, N,N',N'-t'ri(Z-hydroxyethyl) N- octadecenyl propylene diamine, 'N,N,N-tri(2-hydroxyethyl) Nhexadecyl propylene diamine, N,N',N-tri(3 hydroxypropyl) N-octadecadienyl propylene diamine, N, N',N'-tri(Z-hydroxyethyl) N-octadecyl ethylene diamine, N,N,N'-tri(2-hydroxyethyl) N-octadecenyl ethylene diamine, N,N,N-tri(Z-hydroxyethyl) N-tetradecyl propyle'ne diamine, 'N
- the monoand diamines may be used individually or as mixtures. Mixtures may vary from to 90 weight percent of either monoor diamines.
- Alkaline earth metal carbonates are magnesium, calcium and barium carbonates, preferably calcium and barium carbonates. Small amounts of the hydroxides of the metals may also be present, usually not contributing more than about 20% of the alkalinity value from the alkaline earth metal carbonate composition.
- the alkaline earth metals are not soluble in hydrocarbon media. Therefore, they are invariably dispersed with some type of metal salt dispersant. These dispersants are well known in the art and will be discussed only summarily.
- the preferred dispersants are the sulfonate and phenate dispersants.
- the sulfonates are extensively discussed in U.S. Pat. No. 3,488,284.
- the organic sulfonates are pre pared either from natural or synthetic sources.
- the natural sulfonates are referred to as mahogany sulfonates and are derived from petroleum mineral oil fractions and normally have from about 25 to 50 carbon atoms per sulfonic acid. Synthetic sources are also employed which are usual- 1y alkylated benzenes having from about 25 to 50 carbon atoms.
- the use of the sulfonates and the method of preparing overbased sulfonates is well known, as already indicated by the above patent.
- Other patents include U.S. Pats. Nos. 3,021,280, 3,256,186, 3,057,896 and 3,312,618.
- the phenates are alkyl-ated phenols either individually or polymerized to a low order of from 2 to '5 alkyl phenols, normally bridged with sulfur, alkylene groups, or di(alkylene) amino groups (Mannich bases).
- the alkyl group on the phenol is normally of at least 8 carbons and usually does not exceed 36 carbon atoms, more usually being in the range of about 12 to 30 carbon atoms.
- the phenoxide in the phenate also contributes to alkalinity value.
- overbased phenates are described in numerous patents such as U.S. Pats. Nos. 3,474,035, 3,429,812, 3,388,063, 3,336,224 and 2,798,852.
- alkaline earth metal alkyl phosphonates and thiophosphonates are the alkaline earth metal alkyl phosphonates and thiophosphonates.
- the phosphonates will normally be at least about 30 carbon atoms and may be as high as 200 carbon atoms, more usually from about 50 to 125 carbon atoms. These overbased phosphonates are described in U.S. Pat. No. 3,312,618.
- dispersants are the succinimides of alkylene polyarnines. These dispersants usually have an alkyl or alkenyl group bonded to the succinimide group of at least 50 carbon atoms and not more than about 200 carbon atoms.
- the alkylene polyamines are normally ethylene or propylene polyamines having from 2 to 6 amino groups, more usually from 3 to 5 amino groups. Carboxylates also find use as dispersants.
- the alkalinity value of the overbased dispersants will usually be at least 150 and not exceed 500, more usually being in the range of about 200 to 450 mg. K-OH/ g.
- the equivalent ratio of base to dispersant will be at least 1 to 1 and more usually at least 1.5 to 1, normally not exceeding about 20 to 1.
- compositions are used in a sufficient amount to provide the desired alkalinity value in the final composition. Therefore, the alkaline earth metal carbonates are prepared as concentrates and then diluted in the lubricating oil medium with the hydroxyalkylated amine to provide the desired end composition.
- oils of lubricating viscosity derived from petroleum or synthetic 4 sources.
- the oils may be paraffinic, naphthenic, asphaltic or combinations thereof.
- Oils of lubricating viscosity normally have viscosities in the range of 35 to 50,000 Saybolt Universal Seconds (SUS) at F., more usually from about 50 to 10,000 SUS at 100 F.
- SUS Saybolt Universal Seconds
- additives are desirably included in the composition. These additives may be pour point depressants, oiliness agents, antioxidants, detergents, particularly succinimides, supra, corrosion inhibitors, extreme pressure agents, etc. Usually, for oils to be used in an engine, the total amount of these additives will range from about 0.1 to 15 weight percent, more usually from about 0.5 to 10 weight percent. The individual additives may vary in amount from about 0.01 to 10 weight percent of the total composition. In concentrates, the weight percent of these additives will usual-1y range from about 0.3 to 30 weight percent.
- a preferred aspect of using the compositions of this invention in lubricating oils is to include in the oil from about 1 to 50 mM./kg. of a dihydrocarbyl phosphorodithioate, wherein the hydrocarbyl groups are from about 4 to 36 carbon atoms.
- the hydrocarbyl groups will be alkyl or alkaryl groups.
- the remaining valence of the phosphorodithioate will usually be satisfied by zinc, but polyalkyleneoxy or a third hydrocarbyl group may also be used.
- Hydrocarbyl is an organic radical composed solely of carbon and hydrogen which may be aliphatic, alicyclic or aromatic. In this invention, the preferred hydrocarbyl groups are free of aliphatic unsaturation.
- lubricating oil compositions were prepared by combining the appropriate amount of alkaline earth metal carbonates, specifically calcium carbonate, dispersed by either a sulfonate or a phenate with N-octadecyl (derived from tallow fatty acids) N,N',N'-tri(2-hydroxyethyl) propylene diamine. (Supplied by Armour & Co.
- Ethoduomeen T-13 the composition also contains about 30% :by weight of the total composition of N-octadecyl [derived from tallow fatty acid] N,N-di(2-hydroxyethyl) amine.)
- N-octadecyl derived from tallow fatty acid
- N,N-di(2-hydroxyethyl) amine These compositions were tested in a variety of tests to establish their eifectiveness as rust and corrosion inhibitors. The following indicates the tests carried out, the comopsitions employed, and the results of these tests.
- the first test is carried out as follows: A GM Oldsmobile oil relief valve (cut lengthwise into halves) is polished with No. 2/0 emery polishing paper, rinsed with CF. hexane and then stored in hexane. The relief valve is then placed in 100 ml. of test oil heated in a beaker at -130 F. for one minute. An acidic solution is provided by combining 9 ml. of a solution prepared from 4 ml. of concentrated hydrochloric acid, 4 ml. of glacial acetic acid, 4 ml. concentrated sulfuric acid and 84 ml. distilled Water with 300 ml. of test oil in a 400 ml. beaker. After stirring at 2000 r.p.m.
- the acid solution and test oil composition are placed in an oil bath maintained at F.
- the treated relief valve is then put into the oil mixture with the flat surface sitting on the bottom of the breaker.
- the beaker is removed from the oil bath, the valve removed from the oil and rinsed twice with C.P. hexane and rated.
- the valve is rated from 0 to 10; 0 equaling heavy rust and 10 being clean.
- the test oil employed, simulating a commercially compounded oil was an SAE 30 oil (26.7 wt. percent 130 neutral oil, 42.8 wt. percent 480 neutral oil and 30.5 wt. percent bright stock; this was the base oil in all the tests unless otherwise indicated) containing 2 weight percent of a polyisobutenyl succinimide of tetraethylene pentamine (the polyisobutenyl group having a number average molecular weight of about 1000), 12 mM./ kg. of zinc dialkyl dithiophosphate (alkyl of from 4 to 5 carbon atoms) and 40 mM./kg. based on Ca. of calcium carbonate dispersed with calcium mahogany sulfonate wherein the base ratio is 9.3, and the calcium carbonate composition contains 11.4% calcium.
- the final composition has an alkalinity value from the calcium carbonate of about 1.45.
- the rust rating for the reference oil without the diamine was 6.5. With 0.3 weight percent of the diamine and 0.15 weight percent of the monoamine, the rust rating was 9.1 and 9.4.
- the Humidity Cabinet Test is ASTM D1748 and employs a sand blasted steel panel /8" x 2" x 4" dipped in the oil to be tested, drained of free oil at room temperature and placed in the humidity cabinet at 120 F. and 100 humidity for the time specified for the results.
- the HBr test employs 3 sand blasted steel panels of the same size as above immersed for no more than 1 second in 0.1% aqueous hydrobromic acid. Within one second of removing the test panels from the hydrobromic acid solution, the test panels are dipped in the oil to be evaluated at room temperature.
- test panels are dipped and removed from the test oil 12 times during a period of 60 seconds, after which they are suspended in air for 4 hours at room temperature and then examined for rusting.
- the results are compared with a commercially available rust inhibitor, tetrapropenyl succinic acid.
- the next series of tests is the MS Sequence Engine Test. This test is part of the GM specifications and requires a rating of 9 per pass. The first test was carried out using the same reference oil as employed in the Half Relief Valve Rust Test and the same amine composition as employed in that test. The average rust rating for the reference formulation was 8.4 and 8.8. The reference formulation with the amine had an average rust rating of 9.2.
- the MS Sequence IIB Engine Test was repeated using a mid-continent 10W base oil containing 1.9 weight percent of the same succinimide employed previously, 6.25 mM./'kg. of zinc dialkylphenyl dithiophosphate (alkyl is polypropenyl of from 12 to 15 carbon atoms), 9.25 mM./kg. of zinc dialkyl dithiophosphate (alkyl is from 4 to 5' carbon atoms) plus the additional additives set forth in the following table:
- N-octadeeyl (derived from tallow fatty acid) N N N tri(2hydroxyethyl) propylene diamine. Additionally, there is .15 wt. percent of N-octadecyl (derived from tallow fatty acid) dicthanolamine.
- the alkalinity value derived from the overbased sulfonate is 1.45 mg.
- Th allralinity value from the overbased phenate is 4.45 mg. KOH/g.
- the alkalinity value from the overbased phenate is 8.9 mg. KOH/g.
- the above results demonstrate that the combination of alkaline earth metal carbonate and the poly(hydroxyalkylated) alkyl amines provide excellent rust protection, not only under the conditions of recognized bench tests, but also under the severe conditions of the MS Sequence IIB Engine Test.
- the amine composition combination with alkaline earth metal carbonate provides a pass under the very rigid specifications set forth by General Motors.
- the use of the amine compositions permits smaller amounts of ash to be introduced into the oil and therefore avoids the problems associated with high ash oils.
- the hydroxyalkylated amine compositions are compatible with a wide range of other lubricating oil additives providing clear bright lubricant V compositions.
- a hydrocarbon lubricating oil composition comprising a major amount of a hydrocarbon oil of lubricating oil viscosity, from 0.05 weight percent to about 3 weight percent of a compound of the formula:
- a is 0 or 1
- R is an aliphatic hydrocarbon group of from 12 to 24 carbon atoms
- U and Y are each alkylene of from 2 to 3 carbon atoms; and sufiicient alkaline earth metal carbonate dispersed in said hydrocarbon oil as an overbased phenate or sulfonate to provide an alkalinity value of from 0.5 to mg. KOH/g.
- composition according to claim 1 wherein R is of from 16 to 18 carbon atoms, U is ethylene and Y is propylene.
- composition according to claim 1 wherein said alkaline earth metal carbonate is calcium carbonate dispersed in said oil with a phenate or sulfonate lubricating oil dispersant.
- composition according to claim 3 wherein said dispersant is a sulfonate dispersant derived from a sulfonic acid of from 25 to 50 carbon atoms.
- composition according to claim 3 wherein said dispersant is a phenate derived from alkylated phenol or polymerized alkylated phenols having from 2 to 5 phenol groups per molecule and an alkyl group of from 12 to 30 carbon atoms.
- a hydrocarbon lubricating oil composition comprising a major amount of a hydrocarbon oil of lubricating oil viscosity, from 0.1 to 2 weight percent of N-aliphatic hydrocarbon substituted amine or N-aliphatic hydrocarbon substituted propylene diamine, wherein the aliphatic hydrocarbon group is of from 16 to 18 carbon atoms and the valences of the amine nitrogen atoms bonded to other than the aliphatic hydrocarbon group or the propylene group are bonded to Z-hydroxyethyl groups; and sufficient calcium carbonate dispersed in said hydrocarbon oil as an overbased phenate or sulfonate to provide an alkalinity value of from about 1 to 20 mg. KOH/ g.
- composition according to claim 6 wherein said calcium carbonate is dispersed by a phenate having from 1 to 5 alkyl phenol groups per molecule and wherein the alkyl group is of from 8 to 36 carbon atoms.
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Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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US4556770A | 1970-06-11 | 1970-06-11 | |
US14283871A | 1971-05-10 | 1971-05-10 | |
US21564372A | 1972-01-05 | 1972-01-05 | |
US00413144A US3856687A (en) | 1970-06-11 | 1973-11-05 | Acid neutralizing accelerating compositions |
US05/485,470 US3933662A (en) | 1970-06-11 | 1974-07-11 | Lubricating oil compositions |
Publications (1)
Publication Number | Publication Date |
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US3711406A true US3711406A (en) | 1973-01-16 |
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ID=27534905
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
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US00045567A Expired - Lifetime US3711406A (en) | 1970-06-11 | 1970-06-11 | Lubricating oil containing an hydroxylated amine and an overbased sulfonate or phenate |
US00215643A Expired - Lifetime US3791971A (en) | 1970-06-11 | 1972-01-05 | Lubricating oil compositions |
US00413144A Expired - Lifetime US3856687A (en) | 1970-06-11 | 1973-11-05 | Acid neutralizing accelerating compositions |
US05/485,470 Expired - Lifetime US3933662A (en) | 1970-06-11 | 1974-07-11 | Lubricating oil compositions |
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US00215643A Expired - Lifetime US3791971A (en) | 1970-06-11 | 1972-01-05 | Lubricating oil compositions |
US00413144A Expired - Lifetime US3856687A (en) | 1970-06-11 | 1973-11-05 | Acid neutralizing accelerating compositions |
US05/485,470 Expired - Lifetime US3933662A (en) | 1970-06-11 | 1974-07-11 | Lubricating oil compositions |
Country Status (5)
Country | Link |
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US (4) | US3711406A (fr) |
CA (1) | CA984371A (fr) |
DE (2) | DE2128655A1 (fr) |
FR (2) | FR2094182B1 (fr) |
GB (2) | GB1347914A (fr) |
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-
1970
- 1970-06-11 US US00045567A patent/US3711406A/en not_active Expired - Lifetime
-
1971
- 1971-05-28 GB GB1811271A patent/GB1347914A/en not_active Expired
- 1971-06-04 FR FR7120364A patent/FR2094182B1/fr not_active Expired
- 1971-06-09 DE DE19712128655 patent/DE2128655A1/de active Pending
-
1972
- 1972-01-05 US US00215643A patent/US3791971A/en not_active Expired - Lifetime
- 1972-11-30 CA CA157,920A patent/CA984371A/en not_active Expired
- 1972-12-23 DE DE2263366A patent/DE2263366C3/de not_active Expired
- 1972-12-28 FR FR7246768A patent/FR2166380A2/fr active Pending
-
1973
- 1973-01-05 GB GB83973A patent/GB1399991A/en not_active Expired
- 1973-11-05 US US00413144A patent/US3856687A/en not_active Expired - Lifetime
-
1974
- 1974-07-11 US US05/485,470 patent/US3933662A/en not_active Expired - Lifetime
Cited By (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3884821A (en) * | 1971-06-21 | 1975-05-20 | Texaco Inc | Polybutenyl-alkylene polyamine-polyalkanol lubricant additive and lubricating compositions containing same |
US3996285A (en) * | 1973-08-27 | 1976-12-07 | Culbertson George S | 1-(N-dihydroxyalkyl) aminoalkylene-2-propenyl substituted hydrocarbons |
US3951854A (en) * | 1974-01-21 | 1976-04-20 | Continental Oil Company | Stabilized analytical standards |
US4089791A (en) * | 1974-05-16 | 1978-05-16 | Texaco Inc. | Lubricating oil composition |
US4097386A (en) * | 1976-04-01 | 1978-06-27 | Chevron Research Company | Lubricating oil additive composition |
US4086172A (en) * | 1976-04-01 | 1978-04-25 | Chevron Research Company | Lubricating oil additive composition |
US4071460A (en) * | 1976-09-10 | 1978-01-31 | Ball Brothers Research Corporation | Lubricants comprising dialkanolamine derivatives |
DE3246123A1 (de) * | 1981-12-14 | 1983-06-16 | The Lubrizol Corp., 44092 Wickliffe, Ohio | Zusammensetzungen aus hydroxyaminen und carboxyl-dispersants und ihre verwendung als treibstoffzusaetze |
US4915857A (en) * | 1987-05-11 | 1990-04-10 | Exxon Chemical Patents Inc. | Amine compatibility aids in lubricating oil compositions |
US5049290A (en) * | 1987-05-11 | 1991-09-17 | Exxon Chemical Patents Inc. | Amine compatibility aids in lubricating oil compositions |
US4929374A (en) * | 1987-09-22 | 1990-05-29 | Shell Oil Company | Lubricating oil composition |
EP0351964A1 (fr) | 1988-06-24 | 1990-01-24 | Exxon Chemical Patents Inc. | Combinaison synergique d'additifs utile dans les compositions de transmission de puissance |
US5078893A (en) * | 1988-06-24 | 1992-01-07 | Exxon Chemical Patents Inc. | Synergistic combination of additives useful in power transmitting compositions |
EP0611818A1 (fr) | 1990-07-31 | 1994-08-24 | Exxon Chemical Patents Inc. | Produits de réaction contenant un mélange de phosphore et de soufre préparés à pression réduite utiles dans des compositions de transmission de puissance et procédé pour leur préparation |
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 |
US5698722A (en) * | 1992-12-17 | 1997-12-16 | Exxon Chemical Patents Inc. | Functionalization of polymers based on Koch chemistry and derivatives thereof |
US5696064A (en) * | 1992-12-17 | 1997-12-09 | Exxon Chemical Patents Inc. | Functionalization of polymers based on Koch chemistry and derivatives thereof |
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 |
US5334775A (en) * | 1993-06-02 | 1994-08-02 | Exxon Chemical Patents Inc. | Polymer Alkylation of hydroxyaromatic compounds |
US5397486A (en) * | 1993-07-30 | 1995-03-14 | Chevron Chemical Company | Lubricating oil compositions for railroad diesel engines |
US5585030A (en) * | 1993-12-20 | 1996-12-17 | Exxon Chemical Patents Inc. | Increasing the friction durability of power transmission fluids through the use of oil soluble competing additives |
US5582761A (en) * | 1993-12-20 | 1996-12-10 | Exxon Chemical Patents Inc. | Increasing the friction durability of power transmission fluids through the use of oil soluble competing additives |
US5783735A (en) * | 1994-06-17 | 1998-07-21 | Exxon Chemical Patents Inc. | Process for preparing polymeric amides useful as additives in fuels and lubricating oils |
US5767046A (en) * | 1994-06-17 | 1998-06-16 | Exxon Chemical Company | Functionalized additives useful in two-cycle engines |
US5756431A (en) * | 1994-06-17 | 1998-05-26 | Exxon Chemical Patents Inc | Dispersants derived from heavy polyamine and second amine |
US5804667A (en) * | 1994-06-17 | 1998-09-08 | Exxon Chemical Patents Inc. | Dispersant additives and process |
US5854186A (en) * | 1994-06-17 | 1998-12-29 | Exxon Chemical Patents, Inc. | Lubricating oil dispersants derived from heavy polyamine |
US5872084A (en) * | 1994-06-17 | 1999-02-16 | Exxon Chemical Patents, Inc. | Dispersants derived from heavy polyamine and second amine |
US5936041A (en) * | 1994-06-17 | 1999-08-10 | Exxon Chemical Patents Inc | Dispersant additives and process |
WO1999036491A1 (fr) | 1998-01-13 | 1999-07-22 | Exxon Chemical Patents Inc. | Fluides de transmission automatique aux proprietes viscometriques ameliorees |
US6750185B2 (en) * | 2001-04-02 | 2004-06-15 | Tonengeneral Sekiyu K.K. | Lubricating oil composition for internal combustion engines |
Also Published As
Publication number | Publication date |
---|---|
CA984371A (en) | 1976-02-24 |
DE2263366A1 (de) | 1973-07-12 |
DE2263366C3 (de) | 1979-09-20 |
US3933662A (en) | 1976-01-20 |
DE2128655A1 (de) | 1971-12-16 |
US3791971A (en) | 1974-02-12 |
GB1399991A (en) | 1975-07-02 |
US3856687A (en) | 1974-12-24 |
GB1347914A (en) | 1974-02-27 |
FR2094182B1 (fr) | 1975-08-22 |
DE2263366B2 (de) | 1979-01-18 |
FR2094182A1 (fr) | 1972-02-04 |
FR2166380A2 (fr) | 1973-08-17 |
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