US2820010A - Lubricating compositions - Google Patents

Lubricating compositions Download PDF

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US2820010A
US2820010A US527876A US52787655A US2820010A US 2820010 A US2820010 A US 2820010A US 527876 A US527876 A US 527876A US 52787655 A US52787655 A US 52787655A US 2820010 A US2820010 A US 2820010A
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oil
soluble
silver
compositions
lubricating oil
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US527876A
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Bergstrom Roland Frederick
Harvey M Trowbridge
Robert C Jones
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Shell Development Co
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Shell Development Co
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/027Neutral salts thereof
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/028Overbased salts thereof
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/34Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • C10M2207/402Castor oils
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • C10M2207/404Fatty vegetable or animal oils obtained from genetically modified species
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
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    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/101Condensation polymers of aldehydes or ketones and phenols, e.g. Also polyoxyalkylene ether derivatives thereof
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
    • C10M2215/065Phenyl-Naphthyl amines
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/067Polyaryl amine alkanes
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/068Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings having amino groups bound to polycyclic aromatic ring systems, i.e. systems with three or more condensed rings
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/046Overbased sulfonic acid salts
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/042Metal salts thereof
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/12Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of organic compounds, e.g. with PxSy, PxSyHal or PxOy
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    • C10M2225/00Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2225/04Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of macromolecualr compounds not containing phosphorus in the monomers
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    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/041Siloxanes with specific structure containing aliphatic substituents

Definitions

  • This invention relates to new and improved lubricating compositions. More particularly, it relates to highly detergent mineral oil lubricating compositions which are non-corrosive and wear resistant to metals such as silver and alloys of silver, copper and lead containing metal and the like.
  • one of the best additive combinations for imparting detergency to lubricants is the combination of a particular class of oil-soluble metal sulfonates and oil-soluble metal phenates.
  • the supplemental use of conventional antioxidants, corrosion and wear inhibitors such as nitrogen-sulfur-containing compounds such as thiocarbamates or organic thiophosphates such as zinc or calcium dialkyl dithiophosphates and the like although effective in inhibiting oxidation, corrosion and/ or wear of conventional metal surfaces such as steel, steel alloys, Babbitt surfaces, cadmium and the like, have been found to be ineffective for oils which contact silver metal-wearing surfaces, such as are used in certain rail road diesel engines, for instance the silver wrist pin bushings, or in aircraft engines which have silver bearing surfaces.
  • the sulfonates are oil-soluble neutral and/ or basic polyvalent metal petroleum sulfonates, of which petroleum sulfonates of the metals of group II of the periodic table having an atomic number of from 12 to 56, inclusive, are preferred, and especially of the alkaline earth metals.
  • Suitable sulfonates include the neutral and/or basic calcium, barium and magnesium petroleum sulfonates of oilsoluble petroleum sulfonic acids.
  • the acids can range in molecular weight from about 350 to 550 and preferably are in the range of from 400 to 500.
  • basic petroleum sulfonates is meant that the amount of neutralizing agent, such as calcium carbonate and/ or calcium hydroxide, which is used to neutralize the petroleum sulfonic acid, is in excess of that which is normally required to neutralize the acid. The excess should be from to 100 and preferably between and 60 percent that normally required to neutralize the acid.
  • neutralizing agent such as calcium carbonate and/ or calcium hydroxide
  • the phenates used in compositions of this invention are oil-soluble neutral and/or basic polyvalent metal polyphenates.
  • polyphenates is meant to include a plurality of phenolic radicals linked together through a carbon such as where a plurality of simple phenates are condensed at positions ortho and/ or para to the phenolic hydroxy group through alkylidene (methylene) radicals.
  • the cationic portion of the phenate can be the same as that in the sulfonate and usually will be, but different cations may be used.
  • the alkaline earth metal salts of the condensation product of an alkylphenol e. g.
  • p-octylphenol with formaldehyde, acetaldehyde or benzaldehyde, e. g. calcium or barium salts of octylphenol-formal- 2,820,010 Patented Jan. 14-, 1958 dehyde condensation products ranging in molecular weight of from 500 to 1100, are particularly suitable and are preferred.
  • the additives which render detergent lubricants of the described class useful in the lubrication of silver and silver alloys constitute a particular class of oil-soluble phosphorus-sulfur-halogen-containing materials.
  • One group of such materials can be prepared by reacting phosphorus sulfide with halogenated fatty materials. Reaction products of this type can be readily prepared by reacting, at temperatures of above 270 F.
  • halogenated fatty materials such as chlorinated sperm oil, chlorinated whale oil, chlorinated degras, or derivatives thereof such as the chlorinated free fatty acids or esters derived from said oils, with a phosphorus sulfide such as P 8 and P 8
  • a phosphorus sulfide such as P 8 and P 8
  • the amount of phosphorus sulfide used in making reaction products of this type should be at least about equivalent to the theoretical amount required to replace the oxygen in the halogenated material. Generally the amount of phosphorus sulfide will be in the range of from 15% to 35% by weight of the halogenated fatty material.
  • reaction product of this type was prepared by reacting chlorinated sperm oil containing 30% by weight chlorine with 20% by weight phosphorus pentasu'lfide at a temperature of about 300 F. for about one hour. The sludge formed was removed and the final oil-soluble product recovered contained phosphorus, sulfur and chlorine.
  • Compounds of this type are commercially available under the trade name Parapoid 16S and contain 7% sulfur, 1.3% chlorine and 4.75% phosphorus.
  • Other examples include reaction products of P 8 or P 8 with chlorinated degras,
  • chlorinated castor oil chlorinated glycerol monoleate
  • chlorinated materials include chlorinated waxes, chlorinated rosins and the like and reacted with P 3 or P 8 as described.
  • Suitable phosphorus-sulfur-halogen containing materials which can be used include additives described in U. S. Patents 2,307,183, 2,494,332 and 2,623,018. Suitable commercially available products are made by Monsanto Chemical Company and sold under the trade name of Santopoid 29, 32 and 33. Suitable materials available under these trade names have the following properties:
  • Such arylarnines preferably have at least two aromatic rings.
  • Preferred compounds are, forv example, the naphthylamines: primary, secondary or tertiary alkyl, aryl or aralkyl naphthylamines in which the alkyl, aryl or aralkyl radicals are attached directly to a nuclear carbon atom of the aromatic nucleus or preferably to the nitrogen atom, suchas phenylalpha, or beta-naphthylamine, tetralin naphthylamine, alpha alpha, alpha beta, or beta beta dinaphthylamines, various phenanthryl-, anthryl-naphthylamines, xenyl naphthylamines, benzyl phenyl naphthylamines, diphenyl naphthylamines, phenyl xenyl naphthththth
  • aryl amines may be used, such as diamino diaryl alkanes, e. g., diamino diphenyl methane, tetrametbyl diamino diphenyl methane, tetra methyl diamino triphenyl methane, tetra ethyl diarnino triphenyl methane, diamino diphenyl ethane, diamino ditolyl ethane, etc., alkylated diaryl amines, e.
  • diamino diaryl alkanes e. g., diamino diphenyl methane, tetrametbyl diamino diphenyl methane, tetra methyl diamino triphenyl methane, tetra ethyl diarnino triphenyl methane, diamino diphenyl ethane, diamino ditolyl e
  • p-ethyl diphenylamine g., p-ethyl diphenylamine, m-ethyl diphenylamine, p-isopropyl diphenylamine, monoand poly-amyl, hexyl, heptyl, octyl, nonyl, decyl, hexadecyl, cyclohexyl, methyl cyclohexyl and other alkyl substituted diphenylamines, etc.
  • the base for additives of this invention can be any natural or synthetic material having lubricating properties.
  • the base may be a hydrocarbon oil obtained from a paraflinic, naphthenic, mid-continent or Coastal stock and/ or mixtures thereof.
  • the viscosity of these oils may vary over a Wide range such as from 45 SUS at 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, copolymers of alkylene glycols and alkylene oxides, organic esters, e.
  • the synthetic lubricants may be used as the sole base lubricant or admixed with fixed oils and derivatives thereof.
  • compositions of this invention may be represented by:
  • compositions are illustrative of preferred compositions of this invention:
  • compositions A through F of this invention were tested in a modified four-ball machine similar in principle to the Boerlage apparatus described in Engineering, vol. 136, July 13, 1933, using a rotating steel top ball and 3 silver discs, operated at 700 R. P. M. spindle speed, 50 pound load and 302 F. oil temperature.
  • compositions 1 and 2 Compositions 1 and 2 were also tested for a period of hours in a Model 567-B diesel engine.
  • the conditions of the silver bushings were rated on the basis of a number scale from 0 to 10, with 10 being excellent, indicating no scufiing or removal of silver from the bushing and below 6 signifying failure.
  • compositions A through F rated between 8 and 10, while Composition 1 rated 4 and Composition 2 rated 3; Composition 3 (mineral oil+0.2% wt phenyl-a-naphthylamine-l-ZA% wt.
  • oil-soluble Ca petroleum sulfonate +1.5% wt. oil-soluble Ca salt of octylphenol-formaldehyde condensation product
  • Compositions A and B were also field tested in E. M. D. F-7 freight locomotives using model 567-B engines having silver bushings. After more than 100,000 miles of operation on these compositions, the engines were in excellent condition showing no sign of wear of the silver bushings, while Composition 1 proved unsatisfactory and silver bushing failure was noted in less than 10,000 miles of operation.
  • lubricating oil compositions contemplated herein may contain other agents, such as pour-point depressants, oiliness agents, blooming agents, compounds for enhancing the viscosity index of the lubricating oil, peptizing agents, etc.
  • a lubricating oil composition which is non-corrosive and wear resistant toward silver consisting essentially of a major proportion of mineral lubricating oil containing from 1.2% to 2.4% of oil-soluble calcium petroleum sulfonate, from 1.0% to 1.5% of oil-soluble calcium salt of octyl phenol-formaldehyde condensation product, and from 0.2% to 0.4% each of phenyl-ot-naphthylamine and 0.25% to 0.5% P 8 treated chlorinated sperm oil.
  • a lubricating oil composition which is non-corrosive and wear resistant toward silver, consisting essentially of a major proportion of mineral lubricating oil containing 1.5% of oil-soluble calcium petroleum sulfonate, 1.2% of oil-soluble calcium salt of octyl phenolformaldehyde condensation product, 0.4% of phenyl-otnaphthylamine and 0.5% of P 8 treated chlorinated sperm oil.
  • a lubricating oil composition which is non-corrosive and wear resistant toward silver, consisting essentially of a major proportion of mineral lubricating oil containing 1.2% of oil-soluble calcium petroleum sulfonate, 1.0% of oil-soluble calcium salt of octyl phenyl-formaldehyde condensation product, 0.2% of phenyl-u-naphthylamine and 0.5 of P 8 treated chlorinated sperm oil.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Description

United States Patent LUBRICATING COMPOSITIONS Roland Frederick Bergstrom and Harvey M. Trowbridge,
Martinez, and Robert C. Jones, Berkeley, Calif., assignors to Shell Development Company, New York, N. Y., a corporation of Delaware No Drawing. Application August 11, 1955 Serial No. 527,876
3 Claims. (Cl. 25233.4)
This invention relates to new and improved lubricating compositions. More particularly, it relates to highly detergent mineral oil lubricating compositions which are non-corrosive and wear resistant to metals such as silver and alloys of silver, copper and lead containing metal and the like.
It has been observed that one of the best additive combinations for imparting detergency to lubricants is the combination of a particular class of oil-soluble metal sulfonates and oil-soluble metal phenates. The supplemental use of conventional antioxidants, corrosion and wear inhibitors such as nitrogen-sulfur-containing compounds such as thiocarbamates or organic thiophosphates such as zinc or calcium dialkyl dithiophosphates and the like, although effective in inhibiting oxidation, corrosion and/ or wear of conventional metal surfaces such as steel, steel alloys, Babbitt surfaces, cadmium and the like, have been found to be ineffective for oils which contact silver metal-wearing surfaces, such as are used in certain rail road diesel engines, for instance the silver wrist pin bushings, or in aircraft engines which have silver bearing surfaces.
It has now been discovered that these detergent lubricants containing this particular oil-soluble sulfonate-phenate additive combination can be rendered non-corrosive and wear resistant toward silver surfaces when supplemented with minor amounts of a particular class of phosphorus-sulfur-halogen-containing organic compounds.
The sulfonates are oil-soluble neutral and/ or basic polyvalent metal petroleum sulfonates, of which petroleum sulfonates of the metals of group II of the periodic table having an atomic number of from 12 to 56, inclusive, are preferred, and especially of the alkaline earth metals. Suitable sulfonates include the neutral and/or basic calcium, barium and magnesium petroleum sulfonates of oilsoluble petroleum sulfonic acids. The acids can range in molecular weight from about 350 to 550 and preferably are in the range of from 400 to 500. By basic petroleum sulfonates is meant that the amount of neutralizing agent, such as calcium carbonate and/ or calcium hydroxide, which is used to neutralize the petroleum sulfonic acid, is in excess of that which is normally required to neutralize the acid. The excess should be from to 100 and preferably between and 60 percent that normally required to neutralize the acid.
The phenates used in compositions of this invention are oil-soluble neutral and/or basic polyvalent metal polyphenates. By polyphenates is meant to include a plurality of phenolic radicals linked together through a carbon such as where a plurality of simple phenates are condensed at positions ortho and/ or para to the phenolic hydroxy group through alkylidene (methylene) radicals. The cationic portion of the phenate can be the same as that in the sulfonate and usually will be, but different cations may be used. The alkaline earth metal salts of the condensation product of an alkylphenol (e. g. p-octylphenol) with formaldehyde, acetaldehyde or benzaldehyde, e. g. calcium or barium salts of octylphenol-formal- 2,820,010 Patented Jan. 14-, 1958 dehyde condensation products ranging in molecular weight of from 500 to 1100, are particularly suitable and are preferred.
The additives which render detergent lubricants of the described class useful in the lubrication of silver and silver alloys constitute a particular class of oil-soluble phosphorus-sulfur-halogen-containing materials. One group of such materials can be prepared by reacting phosphorus sulfide with halogenated fatty materials. Reaction products of this type can be readily prepared by reacting, at temperatures of above 270 F. and preferably in the range of 285 to 325 F., halogenated fatty materials such as chlorinated sperm oil, chlorinated whale oil, chlorinated degras, or derivatives thereof such as the chlorinated free fatty acids or esters derived from said oils, with a phosphorus sulfide such as P 8 and P 8 The amount of phosphorus sulfide used in making reaction products of this type should be at least about equivalent to the theoretical amount required to replace the oxygen in the halogenated material. Generally the amount of phosphorus sulfide will be in the range of from 15% to 35% by weight of the halogenated fatty material. For example, a reaction product of this type was prepared by reacting chlorinated sperm oil containing 30% by weight chlorine with 20% by weight phosphorus pentasu'lfide at a temperature of about 300 F. for about one hour. The sludge formed was removed and the final oil-soluble product recovered contained phosphorus, sulfur and chlorine. Compounds of this type are commercially available under the trade name Parapoid 16S and contain 7% sulfur, 1.3% chlorine and 4.75% phosphorus. Other examples include reaction products of P 8 or P 8 with chlorinated degras,
chlorinated castor oil, chlorinated glycerol monoleate,
methyl dichlorostearate and mixtures thereof. Other chlorinated materials include chlorinated waxes, chlorinated rosins and the like and reacted with P 3 or P 8 as described.
Other suitable phosphorus-sulfur-halogen containing materials which can be used include additives described in U. S. Patents 2,307,183, 2,494,332 and 2,623,018. Suitable commercially available products are made by Monsanto Chemical Company and sold under the trade name of Santopoid 29, 32 and 33. Suitable materials available under these trade names have the following properties:
Santopoid Property Color, ASIM (diluted) 8 5% 5 Pour point, F 5 +5 +25 Flash point, F. (0. O. C.) 250 250 250 Snecific gravity at G0l60 F 1. 09 1.18 1.14 Visc sity S. U. S. at 100 F 268 2, 400 550 S. U. S. at 210 F. 48 59 Sulfur, percent wt- 8.5 8. 2 8. 5 Ohorine, percent wt 24. 0 26. 0 26. 0 Ph sphorus, percent 0.56 0.56 0. 55 Metals, percent wt None None None Still another phosphorus-sulfur-chlorine-containing material which is commercialy available as Anglamol 88, made by Lubrizol Corporation, and which contains 3% sulfur, 18% chlorine and 0.3% phosphorus. This product can be also used in compositions of the present invention.
The addition of minor amounts ofarylamines to thev above additive combination is essential. Such arylarnines preferably have at least two aromatic rings. Preferred compounds are, forv example, the naphthylamines: primary, secondary or tertiary alkyl, aryl or aralkyl naphthylamines in which the alkyl, aryl or aralkyl radicals are attached directly to a nuclear carbon atom of the aromatic nucleus or preferably to the nitrogen atom, suchas phenylalpha, or beta-naphthylamine, tetralin naphthylamine, alpha alpha, alpha beta, or beta beta dinaphthylamines, various phenanthryl-, anthryl-naphthylamines, xenyl naphthylamines, benzyl phenyl naphthylamines, diphenyl naphthylamines, phenyl xenyl naphthylamines, dixenyl naphthylamines; also various phenanthryl, anthryl or picyl phenyl amines, etc. The N-aryl substituted naphthylamines are in general more useful for the present purpose.
If desired, however, other aryl amines may be used, such as diamino diaryl alkanes, e. g., diamino diphenyl methane, tetrametbyl diamino diphenyl methane, tetra methyl diamino triphenyl methane, tetra ethyl diarnino triphenyl methane, diamino diphenyl ethane, diamino ditolyl ethane, etc., alkylated diaryl amines, e. g., p-ethyl diphenylamine, m-ethyl diphenylamine, p-isopropyl diphenylamine, monoand poly-amyl, hexyl, heptyl, octyl, nonyl, decyl, hexadecyl, cyclohexyl, methyl cyclohexyl and other alkyl substituted diphenylamines, etc.
The base for additives of this invention can be any natural or synthetic material having lubricating properties. Thus, the base may be a hydrocarbon oil obtained from a paraflinic, naphthenic, mid-continent or Coastal stock and/ or mixtures thereof. The viscosity of these oils may vary over a Wide range such as from 45 SUS at 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, copolymers of alkylene glycols and alkylene oxides, organic esters, e. g., 2-ethyl hexyl sebacate, dioctyl phthalate, trioctyl phosphate; polymeric tetrahydrofuran, polyalkyl silicones, e. g., dimethyl silicone and the like. If desired, the synthetic lubricants may be used as the sole base lubricant or admixed with fixed oils and derivatives thereof.
The general formulations of compositions of this invention may be represented by:
Broad Limited range, range percent (percent wt Oil-s luble polyvalent metal polyphenates 005-15 0. 1-6 Oil-soluble polyvalent petroleum sultonates 0. 05-5 Arylanune .i 0. 01-5 0. 05-2 Base 011 (natural and/or synthetic) Balance Balance The following compositions are illustrative of preferred compositions of this invention:
Composition A Percent weight Oil-soluble Ca petroleum sulfonate (40% excess Santopoid 33 (8.5% S, 26% Cl, 0.55% P) 0.25 Mineral lubricating oil Balance Composition C Oil-soluble Ca petroleum sulfonate (40% excess base) 1.2 Oil-soluble Ca salt of octyl phenolformaldehyde condensation product (av. mol wt. 1000)--.." 1.0 .Phenyl-a-naphthylamine 0.2
4 Parapoid 16S 0.5 Mineral lubricating oil--- Balance Composition D Oil-soluble Ca petroleumv sulfonate (40% excess base) 1.2 Oil-soluble Ca salt. of octyl phenolformaldehyde condensation product (av. mol wt. 1000) 1.0. Phenyl-u-naphthylamine 0.2 Santopoid 33" 0.25 Mineral lubricating oil Balance Composition E Oil-soluble Ca petroleum sulfonate (40% excess base) 1.2 Oil-soluble Ca salt of octyl phenolformaldehyde condensation product (av. mol wt. 1000) 1.0 Phenylra-naphthylamine 0.4 Parapoid 165 0.5 Mineral lubricating oil Balance Composition F Oil-soluble Ca petroleum sulfonate (40% excess base) 2.4 Oil-soluble Ca salt of octyl phenolformaldehyde condensation product (av. mol wt. 1000) 1.5 Phenyl-a-naphthylamine 0.2 Anglamol 88 (3% S, 18% Cl, 0.3% phosphorus) 0.25 Mineral lubricating oil Balance The mineral lubricating oil used in Compositions A-F was a solvent refined distillate blend meeting the following specification:
Gravity, API min. 23 Color, ASTM 4-6 Pour point, F max. 0 Flash point, F min. 440 Viscosity, SUS, at 210 F 75-80 Viscosity index min. 55
the lubrication of silver surfaces has been demonstrated by the results of comparative tests.
Compositions A through F of this invention were tested in a modified four-ball machine similar in principle to the Boerlage apparatus described in Engineering, vol. 136, July 13, 1933, using a rotating steel top ball and 3 silver discs, operated at 700 R. P. M. spindle speed, 50 pound load and 302 F. oil temperature. The results showed a reduction in sending and wear of the silver surfaces in the range of from 60% to 90% over similar oil compositions except that the Parapoid 16S, Anglamol 88 and Santopoid 33 were replaced by various amounts ranging from 0.2% to 2% by weight of zinc dialkyl dithiophosphate, or zinc dibutyl-dithiocarbamate (Compositions 1 and 2, respectively) Compositions A through F were also tested for a period of hours in a Model 567-B diesel engine. The conditions of the silver bushings were rated on the basis of a number scale from 0 to 10, with 10 being excellent, indicating no scufiing or removal of silver from the bushing and below 6 signifying failure. Compositions A through F rated between 8 and 10, while Composition 1 rated 4 and Composition 2 rated 3; Composition 3 (mineral oil+0.2% wt phenyl-a-naphthylamine-l-ZA% wt.
oil-soluble Ca petroleum sulfonate+1.5% wt. oil-soluble Ca salt of octylphenol-formaldehyde condensation product) rated 6, indicating failure of the silver bushing.
Compositions A and B were also field tested in E. M. D. F-7 freight locomotives using model 567-B engines having silver bushings. After more than 100,000 miles of operation on these compositions, the engines were in excellent condition showing no sign of wear of the silver bushings, while Composition 1 proved unsatisfactory and silver bushing failure was noted in less than 10,000 miles of operation.
In addition to the additives already described lubricating oil compositions contemplated herein may contain other agents, such as pour-point depressants, oiliness agents, blooming agents, compounds for enhancing the viscosity index of the lubricating oil, peptizing agents, etc.
This application is a continuation-in-part of our copending patent application Serial No. 278,112, filed March 22, 1952, and now abandoned.
We claim as our invention:
1. A lubricating oil composition which is non-corrosive and wear resistant toward silver consisting essentially of a major proportion of mineral lubricating oil containing from 1.2% to 2.4% of oil-soluble calcium petroleum sulfonate, from 1.0% to 1.5% of oil-soluble calcium salt of octyl phenol-formaldehyde condensation product, and from 0.2% to 0.4% each of phenyl-ot-naphthylamine and 0.25% to 0.5% P 8 treated chlorinated sperm oil.
2. A lubricating oil composition which is non-corrosive and wear resistant toward silver, consisting essentially of a major proportion of mineral lubricating oil containing 1.5% of oil-soluble calcium petroleum sulfonate, 1.2% of oil-soluble calcium salt of octyl phenolformaldehyde condensation product, 0.4% of phenyl-otnaphthylamine and 0.5% of P 8 treated chlorinated sperm oil.
3. A lubricating oil composition which is non-corrosive and wear resistant toward silver, consisting essentially of a major proportion of mineral lubricating oil containing 1.2% of oil-soluble calcium petroleum sulfonate, 1.0% of oil-soluble calcium salt of octyl phenyl-formaldehyde condensation product, 0.2% of phenyl-u-naphthylamine and 0.5 of P 8 treated chlorinated sperm oil.
References Cited in the file of this patent UNITED STATES PATENTS 2,307,183 Zimmer et a1. Ian. 5, 1943 2,444,948 Musselman et al. July 13, 1948 2,580,274 Bergstrom et al. Dec. 25, 1951 2,629,693 Barton et a1. Feb. 24, 1953

Claims (1)

1. A LUBRICATING OIL COMPOSITION WHICH IS NON-CORROSIVE AND WATER RESISTANT TOWARD SILVER CONSISTING ESSENTIALLY OF A MAJOR PROPORTION OF MINERAL LUBRICATING OIL CONTAINING FROM 1.2% TO 2.4% OF OIL-SOLUBLE CALCIUM PETROLEUM SULFONATE, FROM 1.0% TO 1.5% OF OIL-SOLUBLE CALCIUM SALT OF OCTYL PHENOL-FORMALDEHYDE CONDENSATION PRODUCT, AND FROM 0.2% TO 0.4% EACH OF PHENYL-A-NAPHTHYLAMINE AND 0.25% TO 0.5% P2S5 TREATED CHLORINATED SPERM OIL.
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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2307183A (en) * 1939-05-09 1943-01-05 Standard Oil Dev Co Extreme pressure lubricant
US2444948A (en) * 1945-05-17 1948-07-13 Standard Oil Co Lubricant
US2580274A (en) * 1947-03-08 1951-12-25 Shell Dev Lubricant
US2629693A (en) * 1947-07-01 1953-02-24 Shell Dev Lubricating composition

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2307183A (en) * 1939-05-09 1943-01-05 Standard Oil Dev Co Extreme pressure lubricant
US2444948A (en) * 1945-05-17 1948-07-13 Standard Oil Co Lubricant
US2580274A (en) * 1947-03-08 1951-12-25 Shell Dev Lubricant
US2629693A (en) * 1947-07-01 1953-02-24 Shell Dev Lubricating composition

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