US2191996A - Lubricating oil - Google Patents

Lubricating oil Download PDF

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Publication number
US2191996A
US2191996A US112295A US11229536A US2191996A US 2191996 A US2191996 A US 2191996A US 112295 A US112295 A US 112295A US 11229536 A US11229536 A US 11229536A US 2191996 A US2191996 A US 2191996A
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United States
Prior art keywords
tri
thiophosphite
alkyl
oil
mono
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Expired - Lifetime
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US112295A
Inventor
Bernard H Shoemaker
Clarence M Loane
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Standard Oil Co
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Standard Oil Co
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Publication date
Application filed by Standard Oil Co filed Critical Standard Oil Co
Priority to US112295A priority Critical patent/US2191996A/en
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Publication of US2191996A publication Critical patent/US2191996A/en
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    • CCHEMISTRY; METALLURGY
    • 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
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • C10M137/10Thio derivatives
    • C10M137/105Thio derivatives not containing metal
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/16Naphthenic acids
    • CCHEMISTRY; METALLURGY
    • 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
    • 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
    • C10M2223/047Thioderivatives not containing metallic elements
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/06Groups 3 or 13

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Rolling Contact Bearings (AREA)

Description

ecz ma-21 asses Fatented Feb. 27, 1940 UNITED STATES PATENT orrlcs LUBBICATING on.
No Drawing. Application November 23,1936, Serial N0. 112,295
8 Claims.
1 ward internal combustion engines having high compression ratios, increased acceleration and increased speed characteristics. The use of the hard metal" bearings has created lubricating and corrosion problems, particularly in connection with highly refined oils, some of which may be very corrosive to the"hard metal bearings.
By highly refined lubricating oils we mean viscous oils which have a minimum viscosity in the range of S. A. E. oils, and which have been subjected to such refining processes such as, for example, solvent extraction, that the paraffiriicity of the oil is markedly increased. It has been found that highly refined lubricating oils cause corrosion to alloy bearings of the cadmium-silver type to the extent of 5 mg./cm and even greater when such bearings are submerged for 25 hours or less in an air agitated oil which has been preoxidized at about 340 F. for 25 to 50 hours. The motor oils may be highly refined lubricating oils as such or mixtures of highly refined lubricating oils with less highly refined lubricating oils, or stated in another way, mixtures of corrosive oils and non-corrosive oils, examples of the latter being lubricating oil fractions from Winkler crude or crudes of the Winkler type.
We'have found that corrosion of hard metal alloy bearings of the cadmium-silver type in the presence of highly refined lubricating-oil can be inhibited by adding to the oil up to 2%, but preferably 0.05% to 0.75%, of certain organic phosphorous materials, particularly the aryl and alkyl derivatives of thiophosphites having the general formula /XB; r-x"-R,
in which X is S and X" and X are either 0 or S, and in which R1, R2 and R3 are either hydrogen, and/or an alkyl radical and/or an aryl radical, and at least one of which is an alkyl radicalor an aryl radical.
Further, our invention contemplates the use of the mono-, diand tri-alkyl or aryl thiophosphites or mixtures thereof, the thiophosphites being the mono-, dior tri-thiophosphite.
Further, our invention contemplates the use of an alkyl and/or an aryl thiophosphite in which one or more of the alkyl and/or aryl radicals have a substituted, hydroxy, mercapto, halogen, alkoxy, aryloxy, thiocyano, iso-thiocyano, amino, alkyl substituted amino, etc. group or groups.
Specific examples of some of the thiophosphites falling within the scope of our invention are:
Mono and/or di and/or tri propyl mono, dior tri-thiophosphite Mono and/or di and/or tri butyl mono-, dior tri-thiophosphite Mono and/or di and/or tri or tri-thiophosphite Mono and/0r di and /or tri hexyl mono-, dior tri-thiophosphite Mono and/or di and /or tri phenyl mono-, dior tri-thiophosphite Mono and/or di and/or tri cresyl mono-, di-, or tri-thiophosphite Dibutyl phenyl mono-, dior tri-thiophosphite .Amyl dicresyl mono, dior tri-thiophosphite and the above with the hereinbefore mentioned substituted groups, for example, mono-, di-, or tri-(chlorophenyl), tri-thiophosphites or mix tures and the mono-, dior tri(chlorobutyl) trithiophosphites or mixtures thereof.
Although the alkyl and/or aryl thiophosphites in general may be employed we prefer to use the alkyl and/or the aryl thiophosphites having 3 .to 6 carbon atoms in each alkyl since the same are the most effective corrosion inhibitors.
The effectiveness of compounds of the above type as corrosion inhibitors is demonstrated by thefollowing test in which they were subjected to conditions which are more severe than those encountered in the actual operation of internal combustion engines.
Weighed cadmium-silver alloy bearings were submerged. in samples of a highly refined oil (preoxidized for 25 .hours at 341 F.) with and without the addition of the compound to be tested and the oil air agitated while maintained at a temperature of 341 F. At regular intervals the cadmium-silver alloy bearings were removed amyl mono-, di-
nes nsistence Room from the bath, washed free' of oil and weighed to determine the loss in weight. The bearinss tested.
Periods of submergence Oil 6 hrs. 16 hrs.
Loss in weight Lou in mi ht ing./cm!) (mm/cm Control fi... l. r i Corrosion started. 8. 1
Control+0.27 trip any thiophosphi te. 0. 0 0. 2
The above results clearly show the corrosion inhibiting effect 01' small amounts of triphenyl tri thiophosphite in a highly refined lubricating oil.
The eifectiveness of the thiophosphites in inhibiting the corrosion of bearing metal alloys of the cadmium-silver type is further demonstrated by another test. In this test weighed bearings of the cadmium-silver alloy are placed in vessels containing a highly refined oil with and without the inhibitor. The oil in each vesselis air agitated and maintained at a temperature of about 341 F. At periodic intervals the bearings are removed from the vessels, washed free of oil and the loss in weight determined. The bearings are then repolished bright, reweighed and again tested for another predetermined period. The control oil used in this test was the same type used in the hereinbefore mentioned test.
Using the above test the following data were obtained:
The above data definitely show the high inhibiting effect of the alkyl thiophosphite.
Although most of the compounds mentioned hereinbefore are oil soluble some may not be completely soluble in the lubricant. We have obtained satisfactory results by suspending the inhibitor in the lubricant by means of a small amount of a peptizing agent, such as aluminum naphthenate, aluminum stearate, etc.
While we have described our invention by using preferred examples thereof we do not wish to be limited by the same except as defined by the appended claims.
We claim: y
1. The method of preventing corrosion to hard metal alloy bearings in the presence of highly refined lubricating oils normally corrosive to such bearings in internal combustion engines which comprises adding to said lubricating .oils in an amount sufilcient to inhibit such corrosion an organic phosphorous compound having the gem eral formula x'-a, r-x -a,
xlll liI in which X is sulfur, X" and X' are elements selected from the group consisting of oxygen and sulfur and R1, Rd and R3 are substituents selected from the gro p consisting of hydrogen, alkyl radicals and aryl radicals, at least one of which is selected from the group consisting of alkyl radicals and aryl radicals.
2. A lubricating oil non-corrosive to hard metal alloy bearings comprising a mineral lubricating oil normally corrosive to said bearings and an organic phosphorus compound having the general formula in which X is sulfur, X and X' are elements selected from the group consisting of oxygen and sulfur and R1, R2 and R3 are substituents selected from the group consisting of hydrogen, alkyl radicals and aryl radicals, at least one of which is selected from the group consisting of alkyl radicals and aryl radicals, said phosphorus compound being added in a small but sufli cient quantity to inhibit the corrosion of said hard metal alloy bearings.
3. A lubricating oil non-corrosive to hard metal alloy bearings comprising a. mineral lubricating oil normally corrosive to said bearings and an alkyl thiophosphite having 3 to 6 carbon atoms in each alkyl radical, said alkyl thiophosphite being added in a small but sufiicient quantity to inhibit the corrosion to said hard metal alloy bearing.
4; A lubricating oil as described in claim 3 in which the alkyl thiophosphite is tri-amyl trithiophosphite.
5. A lubricating oil non-corrosive to hard metal alloy bearings comprising a mineral lubricating oil normally corrosive to said bearings and an aryl thiophosphite, said aryl thiophosphite being added in a small but suiilcient quantity to inhibit the corrosion to said hard metal alloy bearing.
6. A lubricating oil as described in claim 5 in which the aryl thiophosphite is tri-phenyl trithiophosphite.
7. The method of preventing corrosion of bearing metal alloys selected from the group consisting of-cadmium-silver alloys, cadmium-nickel alloys and copper-lead alloys in the presence of highly refined lubricating oils in internal combustion engines which comprises adding to said lubricating oils an alkyl tbiophosphite having 3 to 6 carbon atoms in each alkyl radical in a small but sufficient amount to inhibit said corrosion. 8. The method of preventing corrosion of bear- .ing metal alloys selected from the group consisting of cadmium-silver alloys, cadmium-nickel alloys and copper-lead alloys in the presence of highly refined lubricating oils in internal combustion engines which comprises adding'to said lubricating oils an aryl thiophosphite in a small but sufiicient quantity to inhibit said corrosion. BERNARD H. SHOEMAKER.
CLARENCE M. LOANE.
DISCLAIMER 2,l9l,996.-Bernard H. Shoemaker and Clarence M. Loane, Hammond, Ind. LUBRI- CATING OIL. Patent; dated February 27, 1940. Disclaimer filed April 20, 1942, by the assignee, Standard Oil Company (Indiana). Hereby enters this disclaimer to claims 3 and 4 in said specification.
[Ofiicial Gazette May 19, 1942.]
US112295A 1936-11-23 1936-11-23 Lubricating oil Expired - Lifetime US2191996A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2432095A (en) * 1941-12-29 1947-12-09 Delton R Frey Lubricating composition
US2529304A (en) * 1948-02-19 1950-11-07 Standard Oil Dev Co Extreme pressure lubricants
US2586655A (en) * 1948-03-26 1952-02-19 American Cyanamid Co S-alkoxymethyl-o, o'-dialkyldithiophosphates
US3145176A (en) * 1960-04-11 1964-08-18 Ethyl Corp Organic materials stabilized with a mixture of thiodisphenol and dialkyl phosphonates
US3351554A (en) * 1966-01-25 1967-11-07 Mobil Oil Corp Novel reaction products and organic compositions containing same
US3360463A (en) * 1965-04-15 1967-12-26 Albright & Wilson Mfg Ltd Lubricants containing synergistic wear inhibitors
US4753742A (en) * 1986-03-14 1988-06-28 Mallet & Company, Inc. Lubricating oils for dough dividers and the like and methods of using said oils
US5792733A (en) * 1997-08-14 1998-08-11 The Lubrizol Corporation Antiwear compositions containing phosphorus compounds and olefins

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2432095A (en) * 1941-12-29 1947-12-09 Delton R Frey Lubricating composition
US2529304A (en) * 1948-02-19 1950-11-07 Standard Oil Dev Co Extreme pressure lubricants
US2586655A (en) * 1948-03-26 1952-02-19 American Cyanamid Co S-alkoxymethyl-o, o'-dialkyldithiophosphates
US3145176A (en) * 1960-04-11 1964-08-18 Ethyl Corp Organic materials stabilized with a mixture of thiodisphenol and dialkyl phosphonates
US3360463A (en) * 1965-04-15 1967-12-26 Albright & Wilson Mfg Ltd Lubricants containing synergistic wear inhibitors
US3351554A (en) * 1966-01-25 1967-11-07 Mobil Oil Corp Novel reaction products and organic compositions containing same
US4753742A (en) * 1986-03-14 1988-06-28 Mallet & Company, Inc. Lubricating oils for dough dividers and the like and methods of using said oils
US5792733A (en) * 1997-08-14 1998-08-11 The Lubrizol Corporation Antiwear compositions containing phosphorus compounds and olefins

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