US2719123A - Fluid compositions containing a cyclopolysiloxane - Google Patents

Fluid compositions containing a cyclopolysiloxane Download PDF

Info

Publication number
US2719123A
US2719123A US362697A US36269753A US2719123A US 2719123 A US2719123 A US 2719123A US 362697 A US362697 A US 362697A US 36269753 A US36269753 A US 36269753A US 2719123 A US2719123 A US 2719123A
Authority
US
United States
Prior art keywords
ester
cyclopolysiloxane
saturated aliphatic
soap
aromatic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US362697A
Inventor
Robert L Merker
William A Zisman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US362697A priority Critical patent/US2719123A/en
Application granted granted Critical
Publication of US2719123A publication Critical patent/US2719123A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C10M7/00Solid or semi-solid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single solid or semi-solid substances
    • 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/024Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
    • 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
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic 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
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic 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
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
    • 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
    • C10M2207/28Esters
    • C10M2207/286Esters of polymerised unsaturated 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
    • C10M2207/28Esters
    • C10M2207/34Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
    • 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
    • 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
    • C10M2209/108Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
    • 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
    • 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
    • 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • C10M2219/108Phenothiazine
    • 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
    • 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
    • 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
    • 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
    • C10M2229/042Siloxanes with specific structure containing aromatic substituents
    • 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
    • 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
    • C10M2229/043Siloxanes with specific structure containing carbon-to-carbon double bonds
    • 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
    • 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
    • C10M2229/044Siloxanes with specific structure containing silicon-to-hydrogen bonds
    • 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
    • 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
    • C10M2229/045Siloxanes with specific structure containing silicon-to-hydroxyl bonds
    • 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
    • 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
    • C10M2229/046Siloxanes with specific structure containing silicon-oxygen-carbon bonds
    • 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
    • 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
    • C10M2229/047Siloxanes with specific structure containing alkylene oxide groups
    • 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
    • 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
    • C10M2229/048Siloxanes with specific structure containing carboxyl groups
    • 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
    • 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
    • C10M2229/05Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
    • C10M2229/052Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon containing nitrogen
    • 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
    • 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
    • C10N2010/02Groups 1 or 11
    • 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
    • C10N2010/04Groups 2 or 12
    • 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
    • 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
    • C10N2010/08Groups 4 or 14
    • 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
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/08Solids
    • 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
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • This invention relates to new fluid compositions having lubricating properties, more particularly to improved aliphatic ester oils and greases.
  • the aliphatic ester oils to which reference is made herein and with which the present invention is concerned are liquid saturated aliphatic normal esters of saturated aliphatic carboxylic acids which esters are fur ther defined by the fact that their boiling point is 150 C. or higher.
  • This class of liquid aliphatic esters has been recognized by the art as a source of synthetic lubricating oils and some of these esters have been used with metal soaps for making greases.
  • metal soaps accelerate the thermal oxidation of these liquid aliphatic esters and has added antioxidants to the greases to improve their oxidation stability.
  • the present invention has as an object the provision of a new class of antioxidants for improving the oxidation stability of the aliphatic ester oils which contain metal soaps, especially at elevated temperatures.
  • a further object is the provision of aliphatic ester oil greases which have enhanced oxidation stability at elevated temperatures.
  • the new antioxidants may be trimers, tetramers, pentamers, etc., in which the aromatic groups may be, for example, phenyl, naphthyl, diphenyl, tolyl, xylyl, cyclohexylphenyl, anisyl, phenoxyphenyl, hydroxyphenyl, carboxyphenyl, carbethoxyphenyl, nitrophenyl, aminophenyl, N-methylaminophenyl, N-phenylaminophenyl, etc.
  • the aromatic groups may be, for example, phenyl, naphthyl, diphenyl, tolyl, xylyl, cyclohexylphenyl, anisyl, phenoxyphenyl, hydroxyphenyl, carboxyphenyl, carbethoxyphenyl, nitrophenyl, aminophenyl, N-methylaminophenyl, N-phenylaminophenyl, etc.
  • a preferred group of the aromatic cyclopolysiloxanes are those in which the aromatic groups are aryl or lower alkaryl, more preferably, phenyl and lower alkylphenly, for example, methyl, ethyl, propyl, butyl, tertiary butyl and hexylphenyl groups.
  • lower alkyl groups are present on silicon atoms of the cyclopolysiloxanes they may contain up to 6 carbon atoms, for example, methyl, ethyl, propyl, tertiary butyl, hexyl, etc.
  • hexaphenyl cyclotrisiloxane is to be mentioned in particular, hexaphenyl cyclotrisiloxane.
  • the stability to oxidation, especially at elevated temperatures, e. g. at 80 to 150 C., of the aliphatic ester oil-metal soap compositions can be enhanced by the addition thereto of one of the antioxidant cyclopolysiloxanes in concentrations within the range of about 0.1 and 10% by weight therein, with a preferred general range for the addition of the antioxidant being from about 0.1 to 5% by weight.
  • the amount of the antioxidant added will depend upon the activity of the individual cyclopolysiloxanes and the particular aliphatic ester oil-metal soap composition. Depending upon the particular cyclopolysiloxane compound,'the antioxidant is dissolved to a greater or lesser extent in the aliphatic ester oil or dispersed therein.
  • the aliphatic ester oils of the compositions of the invention may be prepared by complete esterification in known way between the corresponding saturated aliphatic carboxylic acids, for example, butyric, oxalic, adipic, 3- methyladipic, azelaic, tricarballylic acids, etc., and the corresponding saturated aliphatic alcohols, for example, methanol, Z-ethylhexanol, ethyleneglycol, glycerol, pentaethrythritol, etc.; the acids and the alcohols being selected so as to obtain the desired liquid normal ester as will be understood by those skilled in the art.
  • saturated aliphatic carboxylic acids for example, butyric, oxalic, adipic, 3- methyladipic, azelaic, tricarballylic acids, etc.
  • saturated aliphatic alcohols for example, methanol, Z-ethylhexanol, ethyleneglycol,
  • a class of esters of particular interest for the compositions of the present invention are the liquid saturated aliphatic diesters of the saturated aliphatic dicarboxylic acids which have an alkylene chain of 3 or more carbon atoms, more especially those which are straight or branched chain alkyl diesters of the 5 to 12 carbon atom alkylene dicarboxylic acids in which the alkylene chain may be branched or unbranched and which have the general formula:
  • R4. is a bivalent aliphatic hydrocarbon radical or" 3 to 10 carbon atoms chain length.
  • dibasic acids are, for example, 2- methylglutaric, adipic, S-methyladipic, pimelic, Z-ethylglutaric, suberic, azelaic and sebacic acids, etc.
  • liquid aliphatic esters with which the invention is concerned are, for example, ethyl myristate, octadecyl acetate, diethyl oxalate, dipropyl malonate, dibutyl-3-methyl gultarate, diethyl adipate, di-Z-ethylhexyl adipate, diethyl pimelate, di-Z-ethylhexyl azelate, di-Z- ethylhexyl sebacate, di-(3,5,5-trirnethylhexyl) sebacate, 2,4-pentanediol dihexanoate, triamyl tricarbllylate, pentaethryritol tetrahexanoiate, etc.
  • the metal soap in the compositions of the invention may be any of the metal salts of the soap-forming fatty and hydroxy fatty acids, for example, the calcium, strontium, barium, sodium, potassium, lithium, copper, tin, lead, zinc, aluminum, etc., salts of lauric, myristic, palmitic, oleic, ricinoleic, stearic, arachidic, behenic, erucic, l2-hydroxy stearic acid, etc., or of mixtures of these acids.
  • the amount of the metal soap in the com positions may be widely varied and range from as little as about 0.1% by weight up to a practical maximum.
  • the metal soap content of the compositions will generally be from about 5 to 30% by weight, for which usually there is employed one of the alkaline earth or alkali metal soaps, for example,
  • the invention is illustrated in greater detail by the following specific example in which an aromatic cyclopolysiloxane was incorporated in a lithium soap-diester grease and subjected to an accelerated oxidation test to deter-' mine its efficacy as an antioxidant for the'metal soapdiester oil composition at elevated temperatures.
  • the greases were prepared in conventional manner by heating the aliphatic ester oil and metal soap together under stirring to form a clear solution, quickly cooling the solution to form a gel and working the gel through a screen to obtain a grease of uniform consistency (about 10 workings through a Hain Microworker).
  • the antioxidant was mixed into the grease and the whole then worked through the screen as before to obtain uniformity of admixture.
  • control grease or blank was made up to contain the same relative proportion of the metal soap and diester oil but without the presence of the cyclopolysiloxane antioxidant.
  • the accelerated oxidation test was carried out in accordance with Navy Specification AN-G-3a(2) using a Norma-Hoffman bomb apparatus.
  • Example A grease was prepared to contain 16.2 mol per cent (11.12% by weight) lithium stearate, 80.8 mol percent (87.68% by weight) di-2-ethylhexyl sebacate and 3.0 mol per cent (1.2% by weight) hexaphenyl cyclotrisilox-
  • a control grease was made up in the same manner to contain only lithium stearate and di-2-ethylhexyl sebacate in the same relative proportions.
  • the aliphatic ester oil-metal soap compositions of the present invention may be blended with miscible proportions of other lubricating oils, such as petroleum oils and polyoxyalkylene oxides having one or both terminals ending in an alkyl ether group, e. g., the butoxy group.
  • Antioxidants of types other than the aromatic cyclopolysiloxanes may be used in the compositions in conjunction with the latter, such as phenolic and aromatic amine type antioxidants which are active as antioxidants at the lower temperatures, e. g., below 100 C., and thereby will impart supplemental protection to the aliphatic ester oilmetal soap compositions at temperatures occurring during storage or during other low temperature non-operating periods, e.
  • antioxidant compounds of the non-silicon type are dialkyl selenides, e. g., dilauryl selenide, and phenothiazine. Some of these supplemental antioxidant compounds are active at the elevated temperatures also, for example, dilauryl selenide and phenothiazine.
  • a fluid composition comprising a liquid saturated aliphatic normal ester of a saturated aliphatic carboxylic acid, which ester has a boiling point not lower than 150 C., at least about 0.1% by weight of a metal soap and a small amount, suflicient to improve the oxidation stability of the ester-soap composition at elevated temperatures, of an aromatic cyclopolysiloxane in which at least half of the silicon atoms are attached to aromatic groups and any remainder to lower alkyl groups of up to 6 carbon atoms.
  • liquid ester is an alkyl diester of a saturated aliphatic dicarboxylic acid.
  • liquid ester is a branched chain alkyl diester of a saturated aliphatic dicarboxylic acid.
  • a fluid composition comprising a liquid branched chain alkyl diester of a saturated aliphatic dicarboxylic acid, which ester has a boiling point not lower than 150 C., at least about 0.1% by weight of a metal soap and a small amount, sufficient to improve the oxidation stability of the ester-soap composition at elevated temperatures, of a cyclopolysiloxane in which at least half of the silicon atoms are attached to aryl groups and any remainder to lower alkyl groups of up to 6 carbon atoms.
  • a fluid composition comprising a liquid branched chain alkyl diester of a saturated aliphatic dicarboxylic acid, which ester has a boiling point not lower than 150 C., at least about 0.1% by weight of a metal soap and a small amount, sufficient to improve the oxidation stability of the ester-soap composition at elevated temperatures, of hexaphenyl cyclotrisiloxane.
  • a grease composition comprising a liquid branched chain alkyl diester of a dicarboxylic acid of the formula:
  • R4 is a bivalent aliphatic hydrocarbon radical of from 3 to 10 carbon atoms chain length, which ester has a boilingpoint not lower than 150 C. and is thickened with a metal soap selected from the group consisting of alkaline earth and alkali metal soaps, and a small amount, sufiicient to improve the oxidation stability of the ester-soap composition at elevated temperatures, of a cyclopolysiloxane in which at least half of the silicon atoms are attached to phenyl groups and any remainder to lower alkyl groups of up to 6 carbon atoms.

Landscapes

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

Description

nited States atent ice FLUID COMPOSITIONS CONTAINING A CYCLOPOLYSILOXANE Robert L. Merker, Bellevue, Pa., and William A. Zisman, Washington, D. C.
No Drawing. Application June 18, 1953, Serial No. 362,697
9 Claims. (Cl. 252-40.7)
This invention relates to new fluid compositions having lubricating properties, more particularly to improved aliphatic ester oils and greases.
The aliphatic ester oils to which reference is made herein and with which the present invention is concerned are liquid saturated aliphatic normal esters of saturated aliphatic carboxylic acids which esters are fur ther defined by the fact that their boiling point is 150 C. or higher. This class of liquid aliphatic esters has been recognized by the art as a source of synthetic lubricating oils and some of these esters have been used with metal soaps for making greases. The art is also aware that metal soaps accelerate the thermal oxidation of these liquid aliphatic esters and has added antioxidants to the greases to improve their oxidation stability.
The present invention has as an object the provision of a new class of antioxidants for improving the oxidation stability of the aliphatic ester oils which contain metal soaps, especially at elevated temperatures. A further object is the provision of aliphatic ester oil greases which have enhanced oxidation stability at elevated temperatures. Other objects will appear hereinafter from the description of the invention.
We have found that the oxidation stability at elevated temperatures of aliphatic ester oils containing metal soaps can be improved by the addition thereto of small amounts of an aromatic cyclopolysiloxane which contains aromatic groups on at least half of the silicon atoms and lower alkyl groups or any not so substituted. The new antioxidants may be trimers, tetramers, pentamers, etc., in which the aromatic groups may be, for example, phenyl, naphthyl, diphenyl, tolyl, xylyl, cyclohexylphenyl, anisyl, phenoxyphenyl, hydroxyphenyl, carboxyphenyl, carbethoxyphenyl, nitrophenyl, aminophenyl, N-methylaminophenyl, N-phenylaminophenyl, etc. A preferred group of the aromatic cyclopolysiloxanes are those in which the aromatic groups are aryl or lower alkaryl, more preferably, phenyl and lower alkylphenly, for example, methyl, ethyl, propyl, butyl, tertiary butyl and hexylphenyl groups. Where lower alkyl groups are present on silicon atoms of the cyclopolysiloxanes they may contain up to 6 carbon atoms, for example, methyl, ethyl, propyl, tertiary butyl, hexyl, etc. Within this preferred group of aromatic cyclopolysiloxanes is to be mentioned in particular, hexaphenyl cyclotrisiloxane.
The stability to oxidation, especially at elevated temperatures, e. g. at 80 to 150 C., of the aliphatic ester oil-metal soap compositions can be enhanced by the addition thereto of one of the antioxidant cyclopolysiloxanes in concentrations within the range of about 0.1 and 10% by weight therein, with a preferred general range for the addition of the antioxidant being from about 0.1 to 5% by weight. The amount of the antioxidant added will depend upon the activity of the individual cyclopolysiloxanes and the particular aliphatic ester oil-metal soap composition. Depending upon the particular cyclopolysiloxane compound,'the antioxidant is dissolved to a greater or lesser extent in the aliphatic ester oil or dispersed therein.
The aliphatic ester oils of the compositions of the invention may be prepared by complete esterification in known way between the corresponding saturated aliphatic carboxylic acids, for example, butyric, oxalic, adipic, 3- methyladipic, azelaic, tricarballylic acids, etc., and the corresponding saturated aliphatic alcohols, for example, methanol, Z-ethylhexanol, ethyleneglycol, glycerol, pentaethrythritol, etc.; the acids and the alcohols being selected so as to obtain the desired liquid normal ester as will be understood by those skilled in the art. A class of esters of particular interest for the compositions of the present invention are the liquid saturated aliphatic diesters of the saturated aliphatic dicarboxylic acids which have an alkylene chain of 3 or more carbon atoms, more especially those which are straight or branched chain alkyl diesters of the 5 to 12 carbon atom alkylene dicarboxylic acids in which the alkylene chain may be branched or unbranched and which have the general formula:
wherein R4. is a bivalent aliphatic hydrocarbon radical or" 3 to 10 carbon atoms chain length. Illustrative of this latter group of dibasic acids are, for example, 2- methylglutaric, adipic, S-methyladipic, pimelic, Z-ethylglutaric, suberic, azelaic and sebacic acids, etc. Illustrative of the liquid aliphatic esters with which the invention is concerned are, for example, ethyl myristate, octadecyl acetate, diethyl oxalate, dipropyl malonate, dibutyl-3-methyl gultarate, diethyl adipate, di-Z-ethylhexyl adipate, diethyl pimelate, di-Z-ethylhexyl azelate, di-Z- ethylhexyl sebacate, di-(3,5,5-trirnethylhexyl) sebacate, 2,4-pentanediol dihexanoate, triamyl tricarbllylate, pentaethryritol tetrahexanoiate, etc.
The metal soap in the compositions of the invention may be any of the metal salts of the soap-forming fatty and hydroxy fatty acids, for example, the calcium, strontium, barium, sodium, potassium, lithium, copper, tin, lead, zinc, aluminum, etc., salts of lauric, myristic, palmitic, oleic, ricinoleic, stearic, arachidic, behenic, erucic, l2-hydroxy stearic acid, etc., or of mixtures of these acids. The amount of the metal soap in the com positions may be widely varied and range from as little as about 0.1% by weight up to a practical maximum. In the case of lubricating greases, the metal soap content of the compositions will generally be from about 5 to 30% by weight, for which usually there is employed one of the alkaline earth or alkali metal soaps, for example,
calcium, strontium, barium, sodium and lithium stearates. I
The invention is illustrated in greater detail by the following specific example in which an aromatic cyclopolysiloxane was incorporated in a lithium soap-diester grease and subjected to an accelerated oxidation test to deter-' mine its efficacy as an antioxidant for the'metal soapdiester oil composition at elevated temperatures. The greases were prepared in conventional manner by heating the aliphatic ester oil and metal soap together under stirring to form a clear solution, quickly cooling the solution to form a gel and working the gel through a screen to obtain a grease of uniform consistency (about 10 workings through a Hain Microworker). The antioxidant was mixed into the grease and the whole then worked through the screen as before to obtain uniformity of admixture. The control grease or blank was made up to contain the same relative proportion of the metal soap and diester oil but without the presence of the cyclopolysiloxane antioxidant. The accelerated oxidation test was carried out in accordance with Navy Specification AN-G-3a(2) using a Norma-Hoffman bomb apparatus.
, ane.
Example A grease was prepared to contain 16.2 mol per cent (11.12% by weight) lithium stearate, 80.8 mol percent (87.68% by weight) di-2-ethylhexyl sebacate and 3.0 mol per cent (1.2% by weight) hexaphenyl cyclotrisilox- A control grease was made up in the same manner to contain only lithium stearate and di-2-ethylhexyl sebacate in the same relative proportions.
Twenty gram samples of each of the two greases were placed in separate Norma-Hoffman bombs which were then sealed, heated to 100 C. and oxygen pressed thereinto at 110 bombs per square inch. The oxidation test was run for a period of 300 hours during which time the temperature in the bombs was maintained at 100 C.i0.5 C.
Bomb. pressure readings were made at intervals over the 300 hour period, which readings were accurate to :10 p. s. i. Consumption of oxygen by the grease and thereby oxidation of the same is indicated by drop in the oxygen pressure in the bomb. Readings of the pressure in the bomb containing the control grease showed a rather sharp drop even in the earlier stages of the run (up to 50 hours) which was progressive until at the end of the 300 hours the pressure had dropped to 50 pounds per square inch, indicating a substantial amount of oxidation to have taken place in the unprotected grease. On the other hand, pressure readings in the bomb contain ing the grease to which the hexaphenyl cyclotrisiloxane had been added showed a drop in pressure of 18 pounds p. s. i. over the 300 hour period, indicating the cyclopolysiloxane compound to be an eifective antioxidant for the grease.
The aliphatic ester oil-metal soap compositions of the present invention may be blended with miscible proportions of other lubricating oils, such as petroleum oils and polyoxyalkylene oxides having one or both terminals ending in an alkyl ether group, e. g., the butoxy group. Antioxidants of types other than the aromatic cyclopolysiloxanes may be used in the compositions in conjunction with the latter, such as phenolic and aromatic amine type antioxidants which are active as antioxidants at the lower temperatures, e. g., below 100 C., and thereby will impart supplemental protection to the aliphatic ester oilmetal soap compositions at temperatures occurring during storage or during other low temperature non-operating periods, e. g., cyclohexylphenol, p-hydroxy diphenyl, 4-t-butyl-2-phenylphenol, thymol, catechol, phenly-anapthylamine, etc. Other antioxidant compounds of the non-silicon type are dialkyl selenides, e. g., dilauryl selenide, and phenothiazine. Some of these supplemental antioxidant compounds are active at the elevated temperatures also, for example, dilauryl selenide and phenothiazine.
While in the foregoing description we have made reference to certain specific embodiments of the invention, these are intended by way of illustration and not in limitation since the invention may be variously embodied without departing from the spirit or scope of the appended claims.
The invention described herein may be manufactured and used by or for the Government of the United States 4. of America for governmental purposes without the payment of any royalties thereon or therefor.
What we claim is:
1. A fluid composition comprising a liquid saturated aliphatic normal ester of a saturated aliphatic carboxylic acid, which ester has a boiling point not lower than 150 C., at least about 0.1% by weight of a metal soap and a small amount, suflicient to improve the oxidation stability of the ester-soap composition at elevated temperatures, of an aromatic cyclopolysiloxane in which at least half of the silicon atoms are attached to aromatic groups and any remainder to lower alkyl groups of up to 6 carbon atoms.
2. A fluid composition as defined in claim 1, wherein the liquid ester is an alkyl diester of a saturated aliphatic dicarboxylic acid.
3. A fluid composition as defined in claim 1, wherein the liquid ester is a branched chain alkyl diester of a saturated aliphatic dicarboxylic acid.
4. A fluid composition comprising a liquid branched chain alkyl diester of a saturated aliphatic dicarboxylic acid, which ester has a boiling point not lower than 150 C., at least about 0.1% by weight of a metal soap and a small amount, sufficient to improve the oxidation stability of the ester-soap composition at elevated temperatures, of a cyclopolysiloxane in which at least half of the silicon atoms are attached to aryl groups and any remainder to lower alkyl groups of up to 6 carbon atoms.
5. A fluid composition as defined in claim 4, wherein the aryl groups on the silicon atoms of the cyclopolysiloxane are phenyl groups.
6. A fluid composition comprising a liquid branched chain alkyl diester of a saturated aliphatic dicarboxylic acid, which ester has a boiling point not lower than 150 C., at least about 0.1% by weight of a metal soap and a small amount, sufficient to improve the oxidation stability of the ester-soap composition at elevated temperatures, of hexaphenyl cyclotrisiloxane.
7. A grease composition comprising a liquid branched chain alkyl diester of a dicarboxylic acid of the formula:
wherein R4 is a bivalent aliphatic hydrocarbon radical of from 3 to 10 carbon atoms chain length, which ester has a boilingpoint not lower than 150 C. and is thickened with a metal soap selected from the group consisting of alkaline earth and alkali metal soaps, and a small amount, sufiicient to improve the oxidation stability of the ester-soap composition at elevated temperatures, of a cyclopolysiloxane in which at least half of the silicon atoms are attached to phenyl groups and any remainder to lower alkyl groups of up to 6 carbon atoms.
8. A grease composition as defined in claim 7, wherein the cyclopolysiloxane is hexaphenyl cyclotrisiloxane.
9. A grease composition as defined in claim 7, wherein the cyclopolysiloxane is octaphenyl cyclotetrasiloxane.
References Cited in the file of this patent UNITED STATES PATENTS

Claims (1)

1. A FLUID COMPOSITION COMPRISING A LIQUID SATURATED ALIPHATIC NORMAL ESTER OF A SATURATED ALIPHATIC CARBOXYLIC ACID, WHICH ESTER HAS A BOILING POINT NOT LOWER THAN 150* C., AT LEAST ABOUT 0.1% BY WEIGHT OF A METAL SOAP AND A SMALL AMOUNT, SUFFICIENT TO IMPROVE THE OXIDATION STABILITY OF THE ESTER-SOAP COMPOSITION AT ELEVATED TEMPERATURES, OF AN AROMATIC CYCLOPOLYSILOXANE IN WHICH AT LEAST HALF OF THE SILICON ATOMS ARE ATTACHED TO AROMATIC GROUPS AND ANY REMAINDER TO LOWER ALKYL GROUPS OF UP TO 6 CARBON ATOMS.
US362697A 1953-06-18 1953-06-18 Fluid compositions containing a cyclopolysiloxane Expired - Lifetime US2719123A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US362697A US2719123A (en) 1953-06-18 1953-06-18 Fluid compositions containing a cyclopolysiloxane

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US362697A US2719123A (en) 1953-06-18 1953-06-18 Fluid compositions containing a cyclopolysiloxane

Publications (1)

Publication Number Publication Date
US2719123A true US2719123A (en) 1955-09-27

Family

ID=23427158

Family Applications (1)

Application Number Title Priority Date Filing Date
US362697A Expired - Lifetime US2719123A (en) 1953-06-18 1953-06-18 Fluid compositions containing a cyclopolysiloxane

Country Status (1)

Country Link
US (1) US2719123A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2826551A (en) * 1954-01-04 1958-03-11 Simoniz Co Nontangling shampoo
US3308144A (en) * 1963-06-17 1967-03-07 Dow Corning 4, 4'-bis(triorganosilyl)diphenylalkylamines
US3375218A (en) * 1962-12-07 1968-03-26 Union Carbide Corp Nitroarylsilanes and siloxanes
FR2185676A1 (en) * 1972-05-25 1974-01-04 Matsushita Electric Ind Co Ltd
US20100155400A1 (en) * 2006-07-07 2010-06-24 Mark Brian Finnestad Mailbox style sharps container

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2407037A (en) * 1939-10-21 1946-09-03 Frank J Sowa Lubricant and process of lubricating surfaces therewith
US2436347A (en) * 1944-12-30 1948-02-17 Standard Oil Dev Co Grease compositions

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2407037A (en) * 1939-10-21 1946-09-03 Frank J Sowa Lubricant and process of lubricating surfaces therewith
US2436347A (en) * 1944-12-30 1948-02-17 Standard Oil Dev Co Grease compositions

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2826551A (en) * 1954-01-04 1958-03-11 Simoniz Co Nontangling shampoo
US3375218A (en) * 1962-12-07 1968-03-26 Union Carbide Corp Nitroarylsilanes and siloxanes
US3308144A (en) * 1963-06-17 1967-03-07 Dow Corning 4, 4'-bis(triorganosilyl)diphenylalkylamines
FR2185676A1 (en) * 1972-05-25 1974-01-04 Matsushita Electric Ind Co Ltd
US20100155400A1 (en) * 2006-07-07 2010-06-24 Mark Brian Finnestad Mailbox style sharps container
US8584885B2 (en) * 2006-07-07 2013-11-19 Covidien Lp Mailbox style sharps container

Similar Documents

Publication Publication Date Title
US3224971A (en) Borate esters and lubricant compositions containing said esters
US2436347A (en) Grease compositions
US3185644A (en) Lubricating compositions containing amine salts of boron-containing compounds
US3778454A (en) Complex ester
US3267031A (en) Stabilized silicone fluids
US2714092A (en) Lithium base grease containing group ii divalent metal alkyl salicylate, such as zinc alkyl salicylate, as copper corrosion inhibitor
US2719123A (en) Fluid compositions containing a cyclopolysiloxane
US2639266A (en) Lubricating grease comprising a complex ester base and sodium myristate
US2872417A (en) High dropping point lithium base greases
US2964479A (en) Stabilizing mixture of 4, 4'-diaminodiphenyl ether and 2, 4'-diaminodiphenyl ether
US2641577A (en) Lithium-calcium lubricating grease composition
US3112267A (en) Lubricating compositions
US2735816A (en) Fluid compositions containing an
US2910437A (en) Stabilization of lubricants
SU464127A3 (en) Lubricant for gas turbine engines
US3642632A (en) Anthranilic acid esters as lubricant additives
US2889281A (en) Synthetic lubricating composition
US2628949A (en) Stabilized lithium base grease
US3018248A (en) Oxidation inhibited mineral oil compositions
US2983678A (en) Synthetic oil containing a rare earth metal diester phosphate
US3115464A (en) Stabilized lubricants
US3649570A (en) Lubricant compositions
US3223634A (en) Lubricant compositions
US2852466A (en) Grease compositions wherein the thickener comprises a metal salt of an nu-acylaminoorganocarboxylic acid
US3203897A (en) Sodium soap grease containing a zinc salt of a dialkyl dithiophosphate