US2763613A - Lubricating oil containing dicyclopentadienyl iron and an oil soluble organic divalent metal salt - Google Patents

Lubricating oil containing dicyclopentadienyl iron and an oil soluble organic divalent metal salt Download PDF

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US2763613A
US2763613A US389161A US38916153A US2763613A US 2763613 A US2763613 A US 2763613A US 389161 A US389161 A US 389161A US 38916153 A US38916153 A US 38916153A US 2763613 A US2763613 A US 2763613A
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lubricating oil
minor
divalent metal
amount
effective
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US389161A
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Lawrence B Scott
Alan C Nixon
Douglas G Roddick
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Shell Development Co
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Shell Development Co
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    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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    • C10M2207/02—Hydroxy compounds
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    • C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
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    • C10M2227/08—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds
    • C10M2227/081—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds with a metal carbon bond belonging to a ring, e.g. ferocene
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    • C10M2229/04—Siloxanes with specific structure
    • C10M2229/041—Siloxanes with specific structure containing aliphatic substituents
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    • C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
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    • C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/046—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives

Definitions

  • This invention relates to lubricants for use in knockmducing engines such as spark-ignition internal combustron engines. More particularly, this invention pertains to lubricating compositions possessing knock-reducing detergent and anti-Wear properties.
  • an anti-knock agent to a lubricant to act in an auxiliary capacity with a knock-inhibited fuel such as fuels containing tetraethyl lea-d with or without tricresylphosphate, triphenylphosphate, tributylphosphate, in order to economically and effectively increase octane requirement or aid in overcoming the maldistribution problem generally encountered in multi-cylinder engines.
  • a knock-inhibited fuel such as fuels containing tetraethyl lea-d with or without tricresylphosphate, triphenylphosphate, tributylphosphate
  • ferrocene dicyclopentadienyl iron
  • ferrocene compounds when added in minor amounts to lubricating oils, effectively act in the manner described above and in addition, often impart a carryover antiknock effect in cases where ordinary fuels are used later, however, ferrocene compounds have the disadvantage of causing wear.
  • lubricating compositions of this invention which contain minor, but knock-inhibiting amounts of ferrocene compound can be effectively in hibited against wear by addition thereto of a minor amount, generally less than about 5% by weight of oilsoluble metal Salts of organic acidic compounds and/or inorganic acidic compounds containing an organic radical such as metal carboxylates, naphthenates, carbamates, sulfonates, phenates, alcoholates, phosphates, phosphonates and including the thio analogues.
  • the anionic portion of said salts can contain various substituent groups such as halogens, amino, cyano, alkyl, cycloalkyl, radicals and the like.
  • Preferred compounds are the metal sulfonates and/or phenates.
  • Ferrocene, le(C5H5)2, also known as dicyclopentadienyl iron, and the preparation thereof, have been described by T. l. Kealy, and T. L. Pauson, Nature, vol. 168 (1951) p. 1040. Also, R. B. Woodward et al., J. A. C. S. vol. 74 (1952) p. 3458, have described the preparation of various derivatives of ferrocene.
  • Other ferrocene compounds include substituted ferrocenes such as acrylated, carboxylated, halogenated, alkylated, aminated and alcoholated ferrocenes, and the like.
  • the second essential additive in lubricating compositions of this invention include oil-soluble salts (metal and non-metal) of organic acidic compounds or inorganic acids containing organic radicals such as alkali, alkaline earth and heavy metal salts of carboxylic acids, sulfonic acids, naphthenic acids, carbamic acids, phenolic compounds, organic acid phosphates, phosphonic acids and the thio analogues of said acidic compounds.
  • organic radicals such as alkali, alkaline earth and heavy metal salts of carboxylic acids, sulfonic acids, naphthenic acids, carbamic acids, phenolic compounds, organic acid phosphates, phosphonic acids and the thio analogues of said acidic compounds.
  • Preferred are the oil-soluble polyvalent metal sulfonates and phenates such as the Ca, Ba, Mg, Al, Zn and Pb petroleum sulfonate, naphthenate and alkyl phenates.
  • the sulfonates for use in compositions of this invention include petroleum sulfonates described in U. S. Patents 2,280,419, 2,344,988, 2,361,804, 2,375,222, 2,480,638, 2,485,861, 2,509,863, 2,501,731, 2,523,582, and 2,585,520. If desired, the sulfonates can be purified by the methods described in United States Patents 2,441,258 and 2,488,721..
  • the aromatic sulfonates which can be utilized in compositions of this invention include those described in United States Patents 2,411,583, 2,418,894, 2,442,915, 2,483,501, 2,531,325, 2,556,198 and 2,556,848.
  • metal sulfonates include alkali metal sulfonates, alkaline earth metal sulfonates (including magnesium) and other polyvalent metal sulfonates, particularly other divalent metal sulfonates and trivalent metal sulfonates, the sulfonates, the sulfonates of the metals of Group II of the Periodic Table and having an atomic number from 12 to 56 are preferred, and especially of the alkaline earth metals within that group of metals.
  • alkali metal sulfonates alkaline earth metal sulfonates (including magnesium) and other polyvalent metal sulfonates, particularly other divalent metal sulfonates and trivalent metal sulfonates
  • the sulfonates, the sulfonates of the metals of Group II of the Periodic Table and having an atomic number from 12 to 56 are preferred, and especially of the alkaline earth metals within that group of metals.
  • Specific sulfonates which are particularly suitable for use in compositions of this in vention include oil-soluble metal sulfonates such as Na, K, Li, Ca, Ba, Mg, Zn, Al, Zn, Sn, Cr and Co petroleum sulfonate, tetra-tertiary butyl naphthalene sulfonate, diwax benzene sulfonate, stearyl benzene sulfonate, diwax naphthalene sulfonate, diisobutylene sulfonate, tertiary octyl phenol sulfonate, di-tertiary amyl phenol sulfonate, alkylated dibenzothiophene sulfonate and mixtures thereof.
  • oil-soluble metal sulfonates such as Na, K, Li, Ca, Ba, Mg, Zn, Al, Zn, Sn, Cr and
  • phenates suitable for use in compositions of this invention include those described in United States Patents 2,197,833,.2,228,654, 2,280,419, 2,344,988, 2,361,804, 2,410,652, 2,501,991, 2,501,992, and 2,610,982.
  • they can be either simple phenates such as metal alkylphenates (Ca cetylphenate), polar substituted simple phenates (Ca or Zn alkylsalicylates) or polyphenates such as where a plurality of the simple phenates are condensed at positions ortho and/ or para to the" phenolic hydroXy group through alkylidene (methylene) radicals or other suitable divalent non-metallic radicals, such as sulfur or selenium.
  • metal alkylphenates Ca cetylphenate
  • polar substituted simple phenates Ca or Zn alkylsalicylates
  • polyphenates such as where a plurality of the simple phenates are condensed at positions ortho and/ or
  • metal phen'ates are contemplated in the practice of the invention including monoand polyvalent metal phenates, such as the alkali, alkaline earth and heavy metal phenates of which preferred are the polyvalent metal phenates of the metals of Group ll of the Periodic Table andliav-ing an atomic number from 12 to 56, especially the alkaline earth metals within that group of metals.
  • monoand polyvalent metal phenates such as the alkali, alkaline earth and heavy metal phenates of which preferred are the polyvalent metal phenates of the metals of Group ll of the Periodic Table andliav-ing an atomic number from 12 to 56, especially the alkaline earth metals within that group of metals.
  • Illustrative compounds are: Na, K, Li, Ca, Ba, Sr, Mg, Zn, Al, Cd', Ni, Fe, Co cetyl phenate, dibutyl phenate, C14-C1s salicylate, octyl thiophenate, eyclohexyl phenate, cetyl phenol sulfide, waxyl phenate, as well as the above metal salts of the condensation product of alkyl phenol with formaldehyde, acetalde hyde or benzaldehyde, e. g., Ca, Ba or Mgsalts of oc'tyl phenolformaldehyde condensation product ranging in molecular weight of from 500 to 1,100.
  • salts are preferred oil-soluble sodium, calcium, barium, zinc, lead, aluminum, salts of alicyclic acid, e. g., naphthenic acid, fatty acids such as oleic, stearic, phenyl mercapto stearic; aromatic acids, e. g., dibutyl phthalic acid, dioctyl benzoic acid; nitrogencontaining acids, e. g., dibutyl dithiocarbamic acid; or
  • 3 ganic phosphorus-containing acids e. g., di(methy1cyclohexyl) dithiophosphate, butyl trichloromethane phosphonic acid and the like can be used in place of the sulfonates and/or phenates described above or in combination therewith.
  • each of the anti-knock compounds and the salts which can be incorporated into the present base compositions such as lubricating oils or fuels will depend somewhat upon the particular anti-knock compound used, the engine in which the material is to be utilized and the degree anti-knock requirement desired to be met.
  • an effective amount of each of said additives for use in lubricating oils can vary from about 0.01 to about 10% and preferably can vary from about 0.1% to about 5% by Weight or as low as 0.05% and even 0.01% by weight.
  • the base oil of this invention in general will be a mineral lubricating oil, but various natural or synthetic liquid materials having suitable lubricating properties are suit able for use in the compositions of the invention.
  • the base may be a hydrocarbon oil including the paraifinic, naphthenic types as well as mixtures thereof.
  • the viscosity of these oils may vary over a wide range such as from 45 SUS to 100 F. to 100 SUS at 210 F.
  • the hydrocarbon oils may be blended with fixed oils such as castor oil, lard oil and the like and/or with synthetic lubricants such as polymerized olefins, copolymcrs of alkylene glycols and alkylene oxides, organic esters, e.
  • the synthetic lubricants may be used as the sole base lubricant or as the predominant base component or admixed with fixed oils and derivatives thereof.
  • compositions of this invention are illustrated by the following examples:
  • Compositions A through K showed an octane benefit varying from 2 to 18 octane numbers when tested in the CPR and Lauson engines using a primary fuel and in field tests using both a primary and secondary reference fuel.
  • Compositions A, B, C and D were also tested in the CPR and Lauson engines for Wear reducing effects and wear was reduced by from 25% to 75% over a base lubricating oil or lubricating oils containing only about 1.2% ferrocene.
  • compositions of this invention are particularly effective when used in combination with primary fuels such as fuels containingtetraethyl lead (TEL), iron carbonyl, with or Without the added presence of organic phosphates such as a tricresylphosphate, triphenylphosphates, triethylphosphites, or various combustion chamber deposit inhibitors, pre-ignition agents, spark plug anti-foulants, anti-oxidents, and the like.
  • primary fuels such as fuels containingtetraethyl lead (TEL), iron carbonyl
  • organic phosphates such as a tricresylphosphate, triphenylphosphates, triethylphosphites, or various combustion chamber deposit inhibitors, pre-ignition agents, spark plug anti-foulants, anti-oxidents, and the like.
  • a lubricating oil composition comprising a predominant amount of a lubricating oil and a minor, but effective knock-reducing amount of a dicyclopentadienyl iron compound containing only iron, carbon and hydrogen in the molecule, and a minor, but effective, Wear-inhibiting amount of an oil-soluble divalent metal salt of an organic acidic compound selected from the group consisting of divalent metal sulfonates, divalent metal phenates, divalent metal phosphates and divalent metal carboxylates.
  • a lubricating oil composition comprising a predominant amount of a lubricating oil and a minor, but effective, knock-reducing amount of an alkyl dicyclopentadienyl iron and a minor, but effective, wear-inhibiting amount of an oil-soluble divalent metal sulfonate.
  • a lubricating oil composition comprising a predominant amount of a lubricating oil and a minor, but effective, knock-reducing amount of an alkyl dicyclopentadienyl iron and a minor, but effective, wear-inhibiting amount of an oil-soluble divalent metal phenate.
  • a lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, wearinhibiting amount of an oil-soluble divalent metal .sulfonate.
  • a lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, Wear-inhibiting amount of an oil-soluble divalent metal phenate.
  • a lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but efiective, wear-inhibiting amount of an oil-soluble divalent metal naphtlienate.
  • a lubricating oil composition comprising a pre dominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dicyclopentaclienyl iron and a minor, but effective, Wear-inhibiting amount of an oil-soluble divalent metal phosphate.
  • a lubricating oil composition comprising: a predominant amount of a mineral lub oil and a minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, wear inhibiting amount of an oibsoluble alkaline earth metal sulfonote.
  • a lubricating oil composition compri a EH8" dominant amount of a mineral lubricant; .l and a minor, but effective, knock-reducing amount of dicyclopentaclieny] iron and a minor, but effective, wear-inhibiting amount of an oil-soluble alkaline earth metal phenatc.
  • a lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but eifective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, vvear'inhibiting amount of an oil-soluble alkaline earth metal naphthenate.
  • a lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, wear-inhibiting amount of an oil-soluble alkaline earth metal phosphoto.
  • a lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but eftective, knock-reducing amount of dibutyl dicyclopentadienyl iron and a minor, but effective, wearinhibiting amount of an oil-soluble Ca petroleum sulfonate.
  • a lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a 6 minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, Wear-inhibiting amount of an oil-so1uble alkaline earth metal salt of octyl phenol-formaldehyde condensation product and of an oil-soluble alkaline earth metal sulfonate.
  • a lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dibutyl dicyclopentadienyl iron and a minor, but effective, Wearinhibiting amount of an oil-soluble alkaline earth metal salt of octyl phenol-formaldehyde condensation product and of an oil-soluble alkaline earth metal sulfonate.
  • a lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dibutyl dicvclopantadienyl iron and minor, but effective, Wearinhibiting amounts of an oilsoluble Ca of octyl phenoliormaldchyde condensation product and Ca petroleum sulfonate.
  • a lubricating oil composition comprising a predominant amount of a lubricating oil and a minor, but eifective, knock-reducing amount of an alkyl dicyclopentndienyl iron and a minor, but effective, Wear-inhibiting amount of an oil-soluble divalent metal naphthenate.
  • a lubricating oil composition comprising a predominant amount of a lubricating oil and a minor, but effective, knock-reducing amount of an alkyl clicyclopentedienyl iron and a minor, but effective, Wear-inhibiting amount of an oil-soluble divalent metal phosphate.

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Description

United States Patent LUBRICATING OIL ZONTAINING DICYCLO- PENTADHENYL [RUN AND AN OIL SOLU- BLE QRGANIC DIVALEN'I METAL SALT Lawrence B. Scott, Lafayette, Allan G. Nixon, Berkeley, and Douglas G. Rodrlicir, Lafayette, tiaiifl, ass-ignore: to Shell Development Company, New York, N. Y., a corporation of Delaware No Drawing. Application October 29, 1953, Serial No. 389,161
17 Claims. (Cl. 252-325) This invention relates to lubricants for use in knockmducing engines such as spark-ignition internal combustron engines. More particularly, this invention pertains to lubricating compositions possessing knock-reducing detergent and anti-Wear properties.
In many instances it has been found desirable to add an anti-knock agent to a lubricant to act in an auxiliary capacity with a knock-inhibited fuel such as fuels containing tetraethyl lea-d with or without tricresylphosphate, triphenylphosphate, tributylphosphate, in order to economically and effectively increase octane requirement or aid in overcoming the maldistribution problem generally encountered in multi-cylinder engines.
Although ferrocene (dicyclopentadienyl iron) and ferrocene compounds, when added in minor amounts to lubricating oils, effectively act in the manner described above and in addition, often impart a carryover antiknock effect in cases where ordinary fuels are used later, however, ferrocene compounds have the disadvantage of causing wear.
It has been found that lubricating compositions of this invention which contain minor, but knock-inhibiting amounts of ferrocene compound can be effectively in hibited against wear by addition thereto of a minor amount, generally less than about 5% by weight of oilsoluble metal Salts of organic acidic compounds and/or inorganic acidic compounds containing an organic radical such as metal carboxylates, naphthenates, carbamates, sulfonates, phenates, alcoholates, phosphates, phosphonates and including the thio analogues. The anionic portion of said salts can contain various substituent groups such as halogens, amino, cyano, alkyl, cycloalkyl, radicals and the like. Preferred compounds are the metal sulfonates and/or phenates.
The discovery that these salts which normally function a detergents or corrosion inhibitors when used in combination with ferrocene compounds as will be herein described can act as Weaninhibitors is most unexpected since normally salts in general do not possess wear-inhibiting properties.
Ferrocene, le(C5H5)2, also known as dicyclopentadienyl iron, and the preparation thereof, have been described by T. l. Kealy, and T. L. Pauson, Nature, vol. 168 (1951) p. 1040. Also, R. B. Woodward et al., J. A. C. S. vol. 74 (1952) p. 3458, have described the preparation of various derivatives of ferrocene. Other ferrocene compounds include substituted ferrocenes such as acrylated, carboxylated, halogenated, alkylated, aminated and alcoholated ferrocenes, and the like. Thus, diacetylferrocene, ferrocene, dicarboxylic acid, bis-(B- chloropropionyl) ferrocene, diacryloylferrocene, dichloroferrocene, tetrachloroterrocene, diaminoferrocene, dihydroxyferrocene, diethoxyferrocene, dimethylferrocene, diethylferrocene, tetraethylferrocene, diisopropylferrocene, di-n-propylferrocene, dibutylferrocene, di-n-butylferrocene, dioctylferrocene, monopropylmonobutylferrocene, and other substituted ferrocenes are excellent anti-knock agents, when utilized in lubricating oils.
The second essential additive in lubricating compositions of this invention include oil-soluble salts (metal and non-metal) of organic acidic compounds or inorganic acids containing organic radicals such as alkali, alkaline earth and heavy metal salts of carboxylic acids, sulfonic acids, naphthenic acids, carbamic acids, phenolic compounds, organic acid phosphates, phosphonic acids and the thio analogues of said acidic compounds. Preferred are the oil-soluble polyvalent metal sulfonates and phenates such as the Ca, Ba, Mg, Al, Zn and Pb petroleum sulfonate, naphthenate and alkyl phenates.
The sulfonates for use in compositions of this invention include petroleum sulfonates described in U. S. Patents 2,280,419, 2,344,988, 2,361,804, 2,375,222, 2,480,638, 2,485,861, 2,509,863, 2,501,731, 2,523,582, and 2,585,520. If desired, the sulfonates can be purified by the methods described in United States Patents 2,441,258 and 2,488,721.. The aromatic sulfonates which can be utilized in compositions of this invention include those described in United States Patents 2,411,583, 2,418,894, 2,442,915, 2,483,501, 2,531,325, 2,556,198 and 2,556,848. Although various metal sulfonates are contemplated in the practice of the invention, including alkali metal sulfonates, alkaline earth metal sulfonates (including magnesium) and other polyvalent metal sulfonates, particularly other divalent metal sulfonates and trivalent metal sulfonates, the sulfonates, the sulfonates of the metals of Group II of the Periodic Table and having an atomic number from 12 to 56 are preferred, and especially of the alkaline earth metals within that group of metals. Specific sulfonates which are particularly suitable for use in compositions of this in vention include oil-soluble metal sulfonates such as Na, K, Li, Ca, Ba, Mg, Zn, Al, Zn, Sn, Cr and Co petroleum sulfonate, tetra-tertiary butyl naphthalene sulfonate, diwax benzene sulfonate, stearyl benzene sulfonate, diwax naphthalene sulfonate, diisobutylene phenol sulfonate, tertiary octyl phenol sulfonate, di-tertiary amyl phenol sulfonate, alkylated dibenzothiophene sulfonate and mixtures thereof.
The phenates suitable for use in compositions of this invention include those described in United States Patents 2,197,833,.2,228,654, 2,280,419, 2,344,988, 2,361,804, 2,410,652, 2,501,991, 2,501,992, and 2,610,982. Specifically, they can be either simple phenates such as metal alkylphenates (Ca cetylphenate), polar substituted simple phenates (Ca or Zn alkylsalicylates) or polyphenates such as where a plurality of the simple phenates are condensed at positions ortho and/ or para to the" phenolic hydroXy group through alkylidene (methylene) radicals or other suitable divalent non-metallic radicals, such as sulfur or selenium. Although various metal phen'ates are contemplated in the practice of the invention including monoand polyvalent metal phenates, such as the alkali, alkaline earth and heavy metal phenates of which preferred are the polyvalent metal phenates of the metals of Group ll of the Periodic Table andliav-ing an atomic number from 12 to 56, especially the alkaline earth metals within that group of metals. Illustrative compounds are: Na, K, Li, Ca, Ba, Sr, Mg, Zn, Al, Cd', Ni, Fe, Co cetyl phenate, dibutyl phenate, C14-C1s salicylate, octyl thiophenate, eyclohexyl phenate, cetyl phenol sulfide, waxyl phenate, as well as the above metal salts of the condensation product of alkyl phenol with formaldehyde, acetalde hyde or benzaldehyde, e. g., Ca, Ba or Mgsalts of oc'tyl phenolformaldehyde condensation product ranging in molecular weight of from 500 to 1,100.
Although the above salts are preferred oil-soluble sodium, calcium, barium, zinc, lead, aluminum, salts of alicyclic acid, e. g., naphthenic acid, fatty acids such as oleic, stearic, phenyl mercapto stearic; aromatic acids, e. g., dibutyl phthalic acid, dioctyl benzoic acid; nitrogencontaining acids, e. g., dibutyl dithiocarbamic acid; or
3 ganic phosphorus-containing acids, e. g., di(methy1cyclohexyl) dithiophosphate, butyl trichloromethane phosphonic acid and the like can be used in place of the sulfonates and/or phenates described above or in combination therewith.
The quantities of each of the anti-knock compounds and the salts which can be incorporated into the present base compositions such as lubricating oils or fuels will depend somewhat upon the particular anti-knock compound used, the engine in which the material is to be utilized and the degree anti-knock requirement desired to be met. In general, an effective amount of each of said additives for use in lubricating oils can vary from about 0.01 to about 10% and preferably can vary from about 0.1% to about 5% by Weight or as low as 0.05% and even 0.01% by weight.
The base oil of this invention in general will be a mineral lubricating oil, but various natural or synthetic liquid materials having suitable lubricating properties are suit able for use in the compositions of the invention. Thus, the base may be a hydrocarbon oil including the paraifinic, naphthenic types as well as mixtures thereof. The viscosity of these oils may vary over a wide range such as from 45 SUS to 100 F. to 100 SUS at 210 F. The hydrocarbon oils may be blended with fixed oils such as castor oil, lard oil and the like and/or with synthetic lubricants such as polymerized olefins, copolymcrs of alkylene glycols and alkylene oxides, organic esters, e. g., 2-ethylhexy1 sebacate, dioctyl phthalate; polymeric tetrahydrofuran, polyalkyl silicone polymers, e. g., dimethyl silicone polymer and the like. If desired, the synthetic lubricants may be used as the sole base lubricant or as the predominant base component or admixed with fixed oils and derivatives thereof.
Compositions of this invention are illustrated by the following examples:
Composition A Ferrocene percent wt 0.5 Ca petroleum sulfonate percent SA 0.4 Mineral lubricating oil Essentially balance Composition B Dibutyl ferrocene percent wt 0.5 Ca petroleum sulfonate percent SA 1.0 Mineral lubricating oil Essentially balance Composition C Dibutyl ferrocene percent Wt..- 4.3 Ca petroleum sulfonate percent SA 0.4 Ca salt of octyl phenol-formaldehyde condensation product (M. W. 900-1100) percent SA 0.3 Mineral lubricating oil Essentially balance Composition D Dipropyl ferrocene percent wt 0.5 Ca petroleum sulfonate percent SA 0.4 Ca salt of octyl phenol-formaldehyde condensation product (M. W. 900) percent SA 0.3 Phenol-a-naphthylamine percent wt 0.2 Mineral lubricating oil Essentially balance Composition E Dibutyl ferrocene percent wt 8.7 Ca naphthenate percent wt 3.0 Mineral lubricating oil Essentially balance Composition F Ferrocene percent wt 1.5 Zinc di(methy1 cyclohexyDdithio phosphate percent wt 0.2 Mineral lubricating oil Essentially balance Composition G Dibutyl ferrocene percent wt 4.0
Ca stearate percent wt 2.0
Mineral lubricating oil Essentially balance Composition H Ferrocene percent wt" 1.0
Ca petroleum sulfonate percent wt 2.0
Ca naphthenate percent wt 2.0
Mineral lubricating oil Essentially balance Composition 1 Dibutyl ferrocene percent Wt 0.5
Ca petroleum sulfonate percent SA 1.0
Di-Z-ethyl hexyl sebaca-te Essentially balance Composition J Diamyl ferrocene percent wt 2.0
Ba petroleum sulfonate percent Wt 1.0
Mineral lubricating oil Essentially balance Composition K Ferrocene percent Wt 1.0
Ca polyalkyl benzoate percent wt 1.0
Mineral lubricating oil Essentially balance 1 SA: Sulfate Ash.
Compositions A through K showed an octane benefit varying from 2 to 18 octane numbers when tested in the CPR and Lauson engines using a primary fuel and in field tests using both a primary and secondary reference fuel. Compositions A, B, C and D were also tested in the CPR and Lauson engines for Wear reducing effects and wear was reduced by from 25% to 75% over a base lubricating oil or lubricating oils containing only about 1.2% ferrocene.
Compositions of this invention are particularly effective when used in combination with primary fuels such as fuels containingtetraethyl lead (TEL), iron carbonyl, with or Without the added presence of organic phosphates such as a tricresylphosphate, triphenylphosphates, triethylphosphites, or various combustion chamber deposit inhibitors, pre-ignition agents, spark plug anti-foulants, anti-oxidents, and the like.
We claim as our invention:
l. A lubricating oil composition comprising a predominant amount of a lubricating oil and a minor, but effective knock-reducing amount of a dicyclopentadienyl iron compound containing only iron, carbon and hydrogen in the molecule, and a minor, but effective, Wear-inhibiting amount of an oil-soluble divalent metal salt of an organic acidic compound selected from the group consisting of divalent metal sulfonates, divalent metal phenates, divalent metal phosphates and divalent metal carboxylates.
2. A lubricating oil composition comprising a predominant amount of a lubricating oil and a minor, but effective, knock-reducing amount of an alkyl dicyclopentadienyl iron and a minor, but effective, wear-inhibiting amount of an oil-soluble divalent metal sulfonate.
3. A lubricating oil composition comprising a predominant amount of a lubricating oil and a minor, but effective, knock-reducing amount of an alkyl dicyclopentadienyl iron and a minor, but effective, wear-inhibiting amount of an oil-soluble divalent metal phenate.
4. A lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, wearinhibiting amount of an oil-soluble divalent metal .sulfonate.
5. A lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, Wear-inhibiting amount of an oil-soluble divalent metal phenate. V
6. A lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but efiective, wear-inhibiting amount of an oil-soluble divalent metal naphtlienate.
7. A lubricating oil composition comprising a pre dominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dicyclopentaclienyl iron and a minor, but effective, Wear-inhibiting amount of an oil-soluble divalent metal phosphate.
8. A lubricating oil composition comprising: a predominant amount of a mineral lub oil and a minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, wear inhibiting amount of an oibsoluble alkaline earth metal sulfonote.
9. A lubricating oil composition compri a EH8" dominant amount of a mineral lubricant; .l and a minor, but effective, knock-reducing amount of dicyclopentaclieny] iron and a minor, but effective, wear-inhibiting amount of an oil-soluble alkaline earth metal phenatc.
10. A lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but eifective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, vvear'inhibiting amount of an oil-soluble alkaline earth metal naphthenate.
11. A lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, wear-inhibiting amount of an oil-soluble alkaline earth metal phosphoto.
12.. A lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but eftective, knock-reducing amount of dibutyl dicyclopentadienyl iron and a minor, but effective, wearinhibiting amount of an oil-soluble Ca petroleum sulfonate.
l3. A lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a 6 minor, but effective, knock-reducing amount of dicyclopentadienyl iron and a minor, but effective, Wear-inhibiting amount of an oil-so1uble alkaline earth metal salt of octyl phenol-formaldehyde condensation product and of an oil-soluble alkaline earth metal sulfonate.
.14. A lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dibutyl dicyclopentadienyl iron and a minor, but effective, Wearinhibiting amount of an oil-soluble alkaline earth metal salt of octyl phenol-formaldehyde condensation product and of an oil-soluble alkaline earth metal sulfonate.
15. A lubricating oil composition comprising a predominant amount of a mineral lubricating oil and a minor, but effective, knock-reducing amount of dibutyl dicvclopantadienyl iron and minor, but effective, Wearinhibiting amounts of an oilsoluble Ca of octyl phenoliormaldchyde condensation product and Ca petroleum sulfonate.
16. A lubricating oil composition comprising a predominant amount of a lubricating oil and a minor, but eifective, knock-reducing amount of an alkyl dicyclopentndienyl iron and a minor, but effective, Wear-inhibiting amount of an oil-soluble divalent metal naphthenate.
17. A lubricating oil composition comprising a predominant amount of a lubricating oil and a minor, but effective, knock-reducing amount of an alkyl clicyclopentedienyl iron and a minor, but effective, Wear-inhibiting amount of an oil-soluble divalent metal phosphate.
References Cited in the file of this patent UNITED STATES PATENTS 2,010,356 Shappirio Aug. 27, 1935 2,059,567 Evans Nov. 3, 1936 2,272,133 Shappirio Feb. 3, 1942 2,562,845 Reamer July 31, 1951 2,585,520 Van Ess et a1 Feb. 12, 1952 2,629,693 Barton et al. Feb. 24, 1953 2,680,758 Thomas June 8, 1954 2,683,157 Weinmayer July 6, 1954

Claims (1)

1. A LUBRICATING OIL COMPOSITION COMPRISING A PREDOMINANT AMOUNT OF A LUBRICATING OIL AND A MINOR, BUT EFFECTIVE KNOCK-REDUCING AMOUNT OF A DICYCLOPENTADIENYL IRON COMPOUND CONTAINING ONLY IRON, CARBON AND HYDROGEN IN THE MOLECULE, AND A MINOR, BUT EFFECTIVE, WEAR-INHIBITING AMOUNT OF AN OIL-SOLUBLE DIVALENT METAL SALT OF AN ORGANIC ACIDIC COMPOUND SELECTED FROM THE GROUP CONSISTING OF DIVALENT METAL SULFONATES, DIVALENT METAL PHENATES, DIVALENT METAL PHOSPHATES AND DIVALENT METAL CARBOXYLATES.
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Cited By (14)

* Cited by examiner, † Cited by third party
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US2959604A (en) * 1956-10-03 1960-11-08 Ethyl Corp Cyclomatic compounds
US2986520A (en) * 1959-07-28 1961-05-30 Shell Oil Co Hydrophobic oleophilic organo claythickened lubricating oil
US3035978A (en) * 1957-08-12 1962-05-22 Ici Ltd Ferrocene hematinic compositions and therapy
US3108128A (en) * 1957-08-12 1963-10-22 Ici Ltd Tertiary alkyl ferrocenes
US3109852A (en) * 1959-01-07 1963-11-05 Ici Ltd Ferrocene derivatives
US3217019A (en) * 1961-05-22 1965-11-09 Standard Oil Co Monocarboxylic acid diesters of 1, 1'-dialpha-hydroxy methyl ferrocene
US3272607A (en) * 1962-06-15 1966-09-13 Sinclair Research Inc Method of reducing ring wear in compression ignition engines burning residual hydrocarbon fuel
US3481717A (en) * 1968-10-22 1969-12-02 Sinclair Research Inc Gasoline composition
US4226733A (en) * 1978-11-17 1980-10-07 Mobil Oil Corporation Lubricant compositions stabilized against ultra-violet degradation
US5747429A (en) * 1994-12-27 1998-05-05 Tonen Corporation Fluid composition for use in fluid couplings containing at least one ferrocene derivative
WO2015162137A1 (en) * 2014-04-25 2015-10-29 Total Marketing Services Use of a lubricant composition for reducing knocking
WO2016012491A1 (en) 2014-07-24 2016-01-28 Total Marketing Services Lubricating composition comprising an anti-knock compound
WO2023057581A1 (en) 2021-10-07 2023-04-13 Totalenergies Onetech Lubricating composition for preventing or reducing abnormal combustion in an engine
US12460148B2 (en) 2021-10-07 2025-11-04 Totalenergies Onetech Spiro compound as detergent additive in lubricants for motorization systems

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US2010356A (en) * 1931-11-17 1935-08-06 Shell Dev Mixed tertiary ethers
US2059567A (en) * 1933-12-30 1936-11-03 Wakefield & Co Ltd C C Prevention of sludge formation in lubricating oils
US2272133A (en) * 1938-10-24 1942-02-03 Shappirio Sol Metallo organo derivative
US2562845A (en) * 1947-12-12 1951-07-31 Shell Dev Anticorrosion composition
US2585520A (en) * 1948-12-03 1952-02-12 Shell Dev Lubricating compositions containing highly basic metal sulfonates
US2629693A (en) * 1947-07-01 1953-02-24 Shell Dev Lubricating composition
US2680758A (en) * 1952-07-10 1954-06-08 Du Pont Dicyclopentadienylnickel and method
US2683157A (en) * 1952-10-02 1954-07-06 Du Pont Carboxycyclopentadienyl (cyclopentadienyl) iron

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Publication number Priority date Publication date Assignee Title
US2010356A (en) * 1931-11-17 1935-08-06 Shell Dev Mixed tertiary ethers
US2059567A (en) * 1933-12-30 1936-11-03 Wakefield & Co Ltd C C Prevention of sludge formation in lubricating oils
US2272133A (en) * 1938-10-24 1942-02-03 Shappirio Sol Metallo organo derivative
US2629693A (en) * 1947-07-01 1953-02-24 Shell Dev Lubricating composition
US2562845A (en) * 1947-12-12 1951-07-31 Shell Dev Anticorrosion composition
US2585520A (en) * 1948-12-03 1952-02-12 Shell Dev Lubricating compositions containing highly basic metal sulfonates
US2680758A (en) * 1952-07-10 1954-06-08 Du Pont Dicyclopentadienylnickel and method
US2683157A (en) * 1952-10-02 1954-07-06 Du Pont Carboxycyclopentadienyl (cyclopentadienyl) iron

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2959604A (en) * 1956-10-03 1960-11-08 Ethyl Corp Cyclomatic compounds
US3035978A (en) * 1957-08-12 1962-05-22 Ici Ltd Ferrocene hematinic compositions and therapy
US3108128A (en) * 1957-08-12 1963-10-22 Ici Ltd Tertiary alkyl ferrocenes
US3109852A (en) * 1959-01-07 1963-11-05 Ici Ltd Ferrocene derivatives
US2986520A (en) * 1959-07-28 1961-05-30 Shell Oil Co Hydrophobic oleophilic organo claythickened lubricating oil
US3067223A (en) * 1959-07-28 1962-12-04 Shell Oil Co Organometallic derivatives of acid clays
US3217019A (en) * 1961-05-22 1965-11-09 Standard Oil Co Monocarboxylic acid diesters of 1, 1'-dialpha-hydroxy methyl ferrocene
US3272607A (en) * 1962-06-15 1966-09-13 Sinclair Research Inc Method of reducing ring wear in compression ignition engines burning residual hydrocarbon fuel
US3481717A (en) * 1968-10-22 1969-12-02 Sinclair Research Inc Gasoline composition
US4226733A (en) * 1978-11-17 1980-10-07 Mobil Oil Corporation Lubricant compositions stabilized against ultra-violet degradation
US5747429A (en) * 1994-12-27 1998-05-05 Tonen Corporation Fluid composition for use in fluid couplings containing at least one ferrocene derivative
WO2015162137A1 (en) * 2014-04-25 2015-10-29 Total Marketing Services Use of a lubricant composition for reducing knocking
FR3020377A1 (en) * 2014-04-25 2015-10-30 Total Marketing Services LUBRICATING COMPOSITION COMPRISING ANTI-CLIQUETIS COMPOUND
JP2017513995A (en) * 2014-04-25 2017-06-01 トータル・マーケティング・サービシーズ Lubricant composition comprising anti-knock compound
WO2016012491A1 (en) 2014-07-24 2016-01-28 Total Marketing Services Lubricating composition comprising an anti-knock compound
FR3024157A1 (en) * 2014-07-24 2016-01-29 Total Marketing Services LUBRICATING COMPOSITION COMPRISING ANTI-CLIQUETIS COMPOUND
CN106661482A (en) * 2014-07-24 2017-05-10 道达尔销售服务公司 Lubricating composition comprising an anti-knock compound
JP2017524778A (en) * 2014-07-24 2017-08-31 トータル・マーケティング・サービシーズ Lubricant composition comprising anti-knock compound
WO2023057581A1 (en) 2021-10-07 2023-04-13 Totalenergies Onetech Lubricating composition for preventing or reducing abnormal combustion in an engine
FR3127954A1 (en) 2021-10-07 2023-04-14 Totalenergies Marketing Services Lubricating composition for preventing or reducing abnormal combustion in an engine
US12460148B2 (en) 2021-10-07 2025-11-04 Totalenergies Onetech Spiro compound as detergent additive in lubricants for motorization systems

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