US2681313A - Alkyl orthosilicate and alkoxysiloxane base grease compositions - Google Patents

Alkyl orthosilicate and alkoxysiloxane base grease compositions Download PDF

Info

Publication number
US2681313A
US2681313A US145306A US14530650A US2681313A US 2681313 A US2681313 A US 2681313A US 145306 A US145306 A US 145306A US 14530650 A US14530650 A US 14530650A US 2681313 A US2681313 A US 2681313A
Authority
US
United States
Prior art keywords
per cent
weight
alkyl
grease
alkoxysiloxane
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
US145306A
Inventor
William S Kather
Wiener Tibor
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.)
California Research LLC
Original Assignee
California Research LLC
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 California Research LLC filed Critical California Research LLC
Priority to US145306A priority Critical patent/US2681313A/en
Priority to GB2290/51A priority patent/GB706033A/en
Application granted granted Critical
Publication of US2681313A publication Critical patent/US2681313A/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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
    • 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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
    • C10M2201/042Carbon; Graphite; Carbon black halogenated, i.e. graphite fluoride
    • 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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/10Compounds containing silicon
    • C10M2201/102Silicates
    • 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
    • C10M2207/10Carboxylix 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/084Acrylate; Methacrylate
    • 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
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
    • 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
    • C10M2215/062Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups bound to the aromatic ring
    • 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
    • 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
    • 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
    • C10M2215/066Arylene diamines
    • 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
    • C10M2227/00Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/02Esters of silicic 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
    • 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
    • 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
    • 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 lug compositions made or alkoxysiloxanes.
  • Greases prepared from mineral oils have many limitations, particularly where satisfactory lubrication is required at both high and low temperatures.
  • Mineral oil greases can be made to have satisfactory low torque requirements at low temperatures for use in outdoor equipment and in aircraft, but the compositions are extremely volatile and have poor oxidative stability resulting in a short service life. Conversely, mineral oil greases with suitable high temperature properties are too stiff to render service at temperatures much below F.
  • Patent Number 2,448,567 has shown improvement over mineral oil greases.
  • alkyl orthosilicates and the alkyl diesters of dicarboxylic acids possess similar advantages over mineral oils.
  • a large homologous series of the latter fluids are known, and more viscous liquids may be selected for formulation when heavy-duty greases are desired.
  • the more viscous members of the series have undesirably high pour points for low-temperature use as fluids or greases, and their viscosity index is as undesirably low as that of some mineral oils.
  • alkoxysiloxanes which are described and claimed in our copending application, Serial Number 137,264, filed January 6, 1950, owned by the common assignee of these applications, have an extremely low pour point and a high viscosity index. Each also has a high boiling range, a high flash and fire point, a low vapor pressure, good thermal and hydrolytic stability, and excellent lubricating characteristics. These alkoxysiloxanes have the further advantage of possessing outstanding oxidative stability, in the presence of inhibitors, which is superior to any known fluids with the possible exception of the expensive alkylsiloxanes.
  • alkyl orthosilicatesand the alkoxysiloxanes may be grease type lubricatwith alkyl orthosilicates
  • a further object of this invention is to provide inhibitors for stabilizing such greases against oxidation.
  • Another and still further object is to provide such greases in which the alkyl orthosilicates and the alkoxysiloxanes are substantial components.
  • compositions com posed in major portion of an alkyl orthosilicate, an alkoxysiloxane, or mixtures thereof, together with smaller proportions of an alkali metal soap yield superior grease compositions when the constituents are properly blended and inhibited.
  • any aliphatic radical ranging from higher may be used, although there are disadvantages in either extremity of the aliphatic series.
  • the very short aliphatic radicals from methyl greases we prefer to use branched chain aliphatic radicals, particularly those whose branching occurs on a carbon atom close to the silicon nucleus so that a greater degree of steric hindrance is provided.
  • Radicals such as l-ethylpropyl, 2-ethy1butyl, 1,3-dimethylbutyl, 2-methylpentyl, l-methylhexyl, l-ethylpentyl, Z-ethylhexyl, 2-butylhexyl, and l-methyl- 4-ethyloctyl are suitable examples.
  • lubricating compositions of our invention may contain varying amounts of other fluids such as mineral oils.
  • a final composition should contain at least 50 per cent by weight .of orthosilicate or alkoxysiloxane or of both so that the desirable properties of these fluids will be reflected in performance of the grease.
  • Mixtures of neutral fully esterified alkoxysiloxanes may be prepared by using condensed ethyl silicate as a starting material, and a mixture having the greatest degree of polymerization is preferred.
  • the condensed ethyl silicaite preferably stripped of any residual orthosilicate by heating at reduced pressures.
  • the stripped product is then added to a to excess ofthe' desired aliphatic alcohol.
  • ethyl alcohol is evolved, and the resulting of stearic, oleic, palmitic, or similar fatty acids.
  • the soap content may vary from 5 to 25 per cent with the optimum usually ranging within the narrower limits of 8 to 12 per cent, depending 'on the particular fluid selected or the grease properties desired.
  • comprising, or containing laminated or foliated solids in a finelydivided condition, such as graphite, talc, carbon black, or the like, may be added to the soap-silicate compositions in various desired proportions.
  • the phenyl-alpha-naphthylamine is a representative aromatic amine type'oxidation inhibitor.
  • the mixture was heate'drapidly with stirring until solubility was obtained at about 380 F.
  • the solution was cooled rapidly by pouring into a water-cooled metal dish, and a gel structure formed after several minutes. The gel was broken to produce a smooth grease by passing it through a (SO-mesh wirescreen followed by several finer screens up to 200 mesh.
  • Another novel grease in accordance with our invention is:
  • Thefinely dividedsolids describedabove may be added in these examples in desired propor- :tions.
  • any high molecular weight polymer which is soluble in an alkyl orthosilicate or an alkoxysiloxane and which has other generally desirable properties may be employed as the agent to'retard crystallization.
  • the polymer content may vary from to 10 per cent.
  • Aromatic amine and phenol type oxidation inhibitors such as phenyl-alpha-naphthylamine; phenyl beta naphthylamine; p tert butylphenol;.p hydroxy diphenylamine; N,N diphenyl' p phenylenediamine; p isopropoxydiphenylamine; N,l T' di beta naphthyl p phenylenediamine; p aminophenol; and diphenylamine; and other known inhibitors may be employed in our greases.
  • the inhibitor content may vary from ⁇ -6 to 5 per cent.
  • the highand low-temperature performance characteristics of the greases of our invention are excellent and greatly superior to mineral oil greases in overall performance.
  • a grease prepared from Z-ethylhexyl orthosilicate and lithium stearate showed approximately a 1.5 per cent evaporation loss in the standard AN-G-25 test (Military Specification Greas Aircraft and Instruments, for Low and High Temperatures).
  • This grease with oxidation inhibitors withstood a rigorous simulated service test for 3'30 hours, which performance is approximately equal to that of an AN-G-ZES specification product.
  • the allryl orthosilicates and alkoxysiloxanes may be combined with a number of different soaps and the examples are but illustrative. Such greases may also becoinpounded with a variety of different anti-crystallization agents, oxidation inhibitors, rust inhibitors, wear or extreme pressure additives, and the like.
  • a composition of matter a grease containing per centto 75 per cent by weight of an alkyl orthosilicate and 5 per cent to 25 per cent by weight of soaps, said percentages totaling per cent.
  • a compositionof matter a grease containing 95 per cent to '25 per cent by weight of alkyl orthosilicate, 5 per cent to 25 per cent by weight of soap, and small percentages of aromatic amine and phenoltype oxidationand acrylic'resin crystallization inhibitors, said percentages totaling lOi) per cent.
  • a compositionof matter a grease containing 95 per. cent to'75 per cent by weight of an alkyl orthosilicate having from. 5 to 14 carbon atoms per hydrocarbon radical, and 5 per cent to 25 per cent by weight of soap, said percentages totaling 100 per cent.
  • a composition ofmatter a grease containing 95'per cent to '?5 per oentby weight of an organic silicate selected from the group consisting of alkyl' orthosilicates and alkoxysiloxanes, and 5 per cent to 25 per cent by weight of soaps, said percentages totaling 100 per cent.
  • a composition of matter a grease containing 95 per cent to '75 per cent by weight of an organic silicate selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, 5 per cent to 25 per cent by weight of soap, and small percentages of aromatic amine and phenol type oxidation and acrylic resin crystallization inhibitors, said ercentages totaling 100 per cent.
  • an organic silicate selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, 5 per cent to 25 per cent by weight of soap, and small percentages of aromatic amine and phenol type oxidation and acrylic resin crystallization inhibitors, said ercentages totaling 100 per cent.
  • a composition of matter a grease containing 95 per cent to 75 per cent by weight of an organic silicate having from 5 to 14 carbon atoms in branched chain structure in the hydrocarbon radical selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, and 5 per cent to 25 per cent by weight of soap, said percentages totaling 100 per cent.
  • a composition of matter, a grease contain ing 95 per cent to 75 per cent by weight of an alkoxysiloxane and 5 per cent to 25 per cent by weight of soaps, said percentages totaling 100 per cent.
  • a composition of matter a grease containing 95 per cent to 75 per cent by weight of an alkoxysiloxane, 5 per cent to 25 per cent by weight of soap, and small percentages of aromatic amine and phenol type oxidation and acrylic resin crystallization inhibitors, said percentages totaling 100 per cent.
  • a composition of matter a grease containing 95 per cent to 75 per cent by weight of an alkoxysiloxane having from 5 to 14 carbon atoms in the hydrocarbon radical, and 5 per cent to 25 per cent by weight of soap, said percentages totaling 100 per cent.
  • a composition of matter a grease containing a major amount by weight of an organic silicate selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, and minor amounts of soaps, mineral oils, and aromatic amine and phenol type oxidation and acrylic resin crystallization inhibitors.
  • an organic silicate selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, and minor amounts of soaps, mineral oils, and aromatic amine and phenol type oxidation and acrylic resin crystallization inhibitors.
  • a composition of matter a grease containing a major amount by Weight of an organic silicate selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, and minor amounts of a laminated foliated solid in finely divided condition and soap.
  • a composition of matter a grease containing a major amount by weight of an organic silicate selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, a minor amount of soap, and an aromatic amine oxidation inhibitor and of an acrylic resin solution crystallization inhibitor.

Description

iatented June 15, 1954 2,681,313 ALKYL ORTHOSILICATE AND ALKOXY- SILOXANE TIONS BASE GREASE COMPOSI- William S. Kather, San Carlos, and Tibor Wiener, Palo Alto, Calif., assignors, by mesne assignments, to California Res Francisco, Calif.,
N Drawing. Application earch Corporation, San a corporation of Delaware February 20, 1950,
Serial No. 145,306
12 Claims.
, This invention relates to lug compositions made or alkoxysiloxanes.
Greases prepared from mineral oils have many limitations, particularly where satisfactory lubrication is required at both high and low temperatures. Mineral oil greases can be made to have satisfactory low torque requirements at low temperatures for use in outdoor equipment and in aircraft, but the compositions are extremely volatile and have poor oxidative stability resulting in a short service life. Conversely, mineral oil greases with suitable high temperature properties are too stiff to render service at temperatures much below F. Because of the narrow temperature range of petroleum oils, recent work has been directed toward the preparation of greases using various synthetic fluids, and one such group, the branched-chain alkyl diesters of dicarboxylic acids as disclosed in Zisman et a1. Patent Number 2,448,567, has shown improvement over mineral oil greases.
The alkyl orthosilicates and the alkyl diesters of dicarboxylic acids possess similar advantages over mineral oils. However, in comparing the two groups of synthetic fluids where the hydrocarbon radicals are identical, we have found that the alkyl orthosilicates possess superior thermal stability, higher viscosity indices, and better hydrolytic stability than the corresponding alkyl diesters of dicarboxylic acids. A large homologous series of the latter fluids are known, and more viscous liquids may be selected for formulation when heavy-duty greases are desired. However, the more viscous members of the series have undesirably high pour points for low-temperature use as fluids or greases, and their viscosity index is as undesirably low as that of some mineral oils.
In contrast thereto, most of the alkoxysiloxanes which are described and claimed in our copending application, Serial Number 137,264, filed January 6, 1950, owned by the common assignee of these applications, have an extremely low pour point and a high viscosity index. Each also has a high boiling range, a high flash and fire point, a low vapor pressure, good thermal and hydrolytic stability, and excellent lubricating characteristics. These alkoxysiloxanes have the further advantage of possessing outstanding oxidative stability, in the presence of inhibitors, which is superior to any known fluids with the possible exception of the expensive alkylsiloxanes.
These desirable physical properties of the alkyl orthosilicatesand the alkoxysiloxanes may be grease type lubricatwith alkyl orthosilicates A further object of this invention is to provide inhibitors for stabilizing such greases against oxidation.
Another and still further object is to provide such greases in which the alkyl orthosilicates and the alkoxysiloxanes are substantial components.
Other and further objects will be apparent from the following description of this invention.
We have discovered that compositions com posed in major portion of an alkyl orthosilicate, an alkoxysiloxane, or mixtures thereof, together with smaller proportions of an alkali metal soap, yield superior grease compositions when the constituents are properly blended and inhibited. In selecting the particular alkyl orthosilicate or alkoxysiloxane, any aliphatic radical ranging from higher may be used, although there are disadvantages in either extremity of the aliphatic series. The very short aliphatic radicals from methyl greases, we prefer to use branched chain aliphatic radicals, particularly those whose branching occurs on a carbon atom close to the silicon nucleus so that a greater degree of steric hindrance is provided. Radicals such as l-ethylpropyl, 2-ethy1butyl, 1,3-dimethylbutyl, 2-methylpentyl, l-methylhexyl, l-ethylpentyl, Z-ethylhexyl, 2-butylhexyl, and l-methyl- 4-ethyloctyl are suitable examples.
The employment of mixtures or orthosilicates or mixtures of alkoxysiloxanes or mixtures of orthosilicates and alkoxysiloxanes is advantageous to reduce crystallization. It is understood that lubricating compositions of our invention may contain varying amounts of other fluids such as mineral oils. In general, a final composition should contain at least 50 per cent by weight .of orthosilicate or alkoxysiloxane or of both so that the desirable properties of these fluids will be reflected in performance of the grease.
Mixtures of neutral fully esterified alkoxysiloxanes may be prepared by using condensed ethyl silicate as a starting material, and a mixture having the greatest degree of polymerization is preferred. The condensed ethyl silicaite preferably stripped of any residual orthosilicate by heating at reduced pressures. The stripped product is then added to a to excess ofthe' desired aliphatic alcohol. As the reaction proceeds, ethyl alcohol is evolved, and the resulting of stearic, oleic, palmitic, or similar fatty acids. n
The soap content may vary from 5 to 25 per cent with the optimum usually ranging within the narrower limits of 8 to 12 per cent, depending 'on the particular fluid selected or the grease properties desired. comprising, or containing laminated or foliated solids in a finelydivided condition, such as graphite, talc, carbon black, or the like, may be added to the soap-silicate compositions in various desired proportions.
An illustrative example-of a novel grease in accordance with our invention is:
Eighty-five and five-tenths arts of 2-ethylhexyl orthosilicate, 10 parts of lithium stearate, 4 parts of acrylic resin solution, phenyl-alpha-naphthylamine were mixed together at roomtemperature. The acrylic resin solution used was Acryloid HF 8555, a commeris frequently Compositions consisting of,
and part of cial product of Rohm and Haas Company, which is included to render the grease more compatible and homogeneous by decreasing the formation of crystals on cooling. The phenyl-alpha-naphthylamine is a representative aromatic amine type'oxidation inhibitor. The mixture was heate'drapidly with stirring until solubility was obtained at about 380 F. The solution was cooled rapidly by pouring into a water-cooled metal dish, and a gel structure formed after several minutes. The gel was broken to produce a smooth grease by passing it through a (SO-mesh wirescreen followed by several finer screens up to 200 mesh.
Another novel grease in accordance with our invention is:
Eightyseven and five-tenths parts of mixed decoxysiloxanes, prepared as described in our c0- pending application previously referred to, 12 parts of aluminum stearate, and part of N,N'- diphenylp-phenylenediamine, an oxidation inhibitor, were mixed at room temperature, and heated rapidly with stirring to about 275 F. when the components were miscible. Rapid cooling was performed by pouring the solution into a cooled metal dish, and a gel formed after several hours. The gel was broken by passing it through wire screens of successively finer mesh.
Thefinely dividedsolids describedabove may be added in these examples in desired propor- :tions.
not critical. In general, it is desirable to heat and cool the mixture as rapidly as possible and heating to the lowest temperature at which solubility is obtained is preferred.
It is apparent that any high molecular weight polymer which is soluble in an alkyl orthosilicate or an alkoxysiloxane and which has other generally desirable properties may be employed as the agent to'retard crystallization. The polymer content may vary from to 10 per cent.
Aromatic amine and phenol type oxidation inhibitors, such as phenyl-alpha-naphthylamine; phenyl beta naphthylamine; p tert butylphenol;.p hydroxy diphenylamine; N,N diphenyl' p phenylenediamine; p isopropoxydiphenylamine; N,l T' di beta naphthyl p phenylenediamine; p aminophenol; and diphenylamine; and other known inhibitors may be employed in our greases. The inhibitor content may vary from {-6 to 5 per cent.
The highand low-temperature performance characteristics of the greases of our invention are excellent and greatly superior to mineral oil greases in overall performance. For example, a grease prepared from Z-ethylhexyl orthosilicate and lithium stearate showed approximately a 1.5 per cent evaporation loss in the standard AN-G-25 test (Military Specification Greas Aircraft and Instruments, for Low and High Temperatures). This grease with oxidation inhibitors withstood a rigorous simulated service test for 3'30 hours, which performance is approximately equal to that of an AN-G-ZES specification product.
The allryl orthosilicates and alkoxysiloxanes may be combined with a number of different soaps and the examples are but illustrative. Such greases may also becoinpounded with a variety of different anti-crystallization agents, oxidation inhibitors, rust inhibitors, wear or extreme pressure additives, and the like.
It is now apparent to those skilled in the art that by the present invention we have provided novel grease compositions satisfyingthe objects above and that changes to the illustrative examples may be made without departing from our inventive concept. Reference should therefore be had to theappended claims to determine the scope of our invention.
What is claimed is:
l. A composition of matter, a grease containing per centto 75 per cent by weight of an alkyl orthosilicate and 5 per cent to 25 per cent by weight of soaps, said percentages totaling per cent.
2. A compositionof matter, a grease containing 95 per cent to '25 per cent by weight of alkyl orthosilicate, 5 per cent to 25 per cent by weight of soap, and small percentages of aromatic amine and phenoltype oxidationand acrylic'resin crystallization inhibitors, said percentages totaling lOi) per cent.
3. A compositionof matter, a grease containing 95 per. cent to'75 per cent by weight of an alkyl orthosilicate having from. 5 to 14 carbon atoms per hydrocarbon radical, and 5 per cent to 25 per cent by weight of soap, said percentages totaling 100 per cent.
4'. A composition ofmatter, a grease containing 95'per cent to '?5 per oentby weight of an organic silicate selected from the group consisting of alkyl' orthosilicates and alkoxysiloxanes, and 5 per cent to 25 per cent by weight of soaps, said percentages totaling 100 per cent.
1 5. A composition of matter, a grease containing 95 per cent to '75 per cent by weight of an organic silicate selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, 5 per cent to 25 per cent by weight of soap, and small percentages of aromatic amine and phenol type oxidation and acrylic resin crystallization inhibitors, said ercentages totaling 100 per cent.
6. A composition of matter, a grease containing 95 per cent to 75 per cent by weight of an organic silicate having from 5 to 14 carbon atoms in branched chain structure in the hydrocarbon radical selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, and 5 per cent to 25 per cent by weight of soap, said percentages totaling 100 per cent.
7. A composition of matter, a grease contain ing 95 per cent to 75 per cent by weight of an alkoxysiloxane and 5 per cent to 25 per cent by weight of soaps, said percentages totaling 100 per cent.
8. A composition of matter, a grease containing 95 per cent to 75 per cent by weight of an alkoxysiloxane, 5 per cent to 25 per cent by weight of soap, and small percentages of aromatic amine and phenol type oxidation and acrylic resin crystallization inhibitors, said percentages totaling 100 per cent.
9. A composition of matter, a grease containing 95 per cent to 75 per cent by weight of an alkoxysiloxane having from 5 to 14 carbon atoms in the hydrocarbon radical, and 5 per cent to 25 per cent by weight of soap, said percentages totaling 100 per cent.
10. A composition of matter, a grease containing a major amount by weight of an organic silicate selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, and minor amounts of soaps, mineral oils, and aromatic amine and phenol type oxidation and acrylic resin crystallization inhibitors.
11. A composition of matter, a grease containing a major amount by Weight of an organic silicate selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, and minor amounts of a laminated foliated solid in finely divided condition and soap.
12. A composition of matter, a grease containing a major amount by weight of an organic silicate selected from the group consisting of alkyl orthosilicates and alkoxysiloxanes, a minor amount of soap, and an aromatic amine oxidation inhibitor and of an acrylic resin solution crystallization inhibitor.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 2,053,474 Graves Sept.8, 1936 2,129,281 Lincoln et a1 Sept. 6, 1938 2,242,400 Loane May 20, 1941 2,274,673 Earle Mar. 3, 1942 2,403,104 Lien July 2, 1946 2,446,177 Hain Aug. 3, 1948 2,450,221 Ashburn Sept. 28, 1948 2,456,642 Merker Dec. 21, 1948 2,486,674 Pederson Nov. 1, 1949 2,490,691 Langkammerer Dec. 6, 1949 2,566,365 Pedlow et a1 Sept. 4, 1951

Claims (2)

1. A COMPOSITION OF MATTER, A GREASE CONTAINING 95 PER CENT TO 75 PER CENT BY WEIGHT OF AN ALKYL ORTHOSILICATE AND 5 PER CENT TO 25 PER CENT BY WEIGHT OF SOAPS, SAID PERCENTAGES TOTALING 100 PER CENT.
11. A COMPOSITION OF MATTER, A GREASE CONTAINING A MAJOR AMOUNT BY WEIGHT OF AN ORGANIC SILICATE SELECTED FROM THE GROUP CONSISTING OF ALKYL ORTHOSILICATES AND ALKOXYSILOXANES, AND MINOR AMOUNTS OF A LIMINATED FOLIATED SOLID IN FINELY DIVIDED CONDITION AND SOAP.
US145306A 1950-02-20 1950-02-20 Alkyl orthosilicate and alkoxysiloxane base grease compositions Expired - Lifetime US2681313A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US145306A US2681313A (en) 1950-02-20 1950-02-20 Alkyl orthosilicate and alkoxysiloxane base grease compositions
GB2290/51A GB706033A (en) 1950-02-20 1951-01-30 Grease compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US145306A US2681313A (en) 1950-02-20 1950-02-20 Alkyl orthosilicate and alkoxysiloxane base grease compositions

Publications (1)

Publication Number Publication Date
US2681313A true US2681313A (en) 1954-06-15

Family

ID=22512492

Family Applications (1)

Application Number Title Priority Date Filing Date
US145306A Expired - Lifetime US2681313A (en) 1950-02-20 1950-02-20 Alkyl orthosilicate and alkoxysiloxane base grease compositions

Country Status (2)

Country Link
US (1) US2681313A (en)
GB (1) GB706033A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2960474A (en) * 1957-05-20 1960-11-15 California Research Corp Silicate-silicone hydraulic fluid composition
US2990367A (en) * 1954-06-21 1961-06-27 Philipp Corp Clay-bodied lubricant containing a silicate ester
US3019191A (en) * 1954-09-28 1962-01-30 California Research Corp Stabilized hydraulic fluid composition
US3091590A (en) * 1953-08-28 1963-05-28 California Research Corp Hydraulic fluid composition
US3146206A (en) * 1962-07-18 1964-08-25 California Research Corp Organosilicon fluid composition
US3350307A (en) * 1964-05-15 1967-10-31 Murex Welding Processes Ltd Lubricating greases
DE1750230A1 (en) * 1968-04-10 1972-04-06 Freudenberg Carl Fa Process to improve the sealing effect of radial sealing rings against lubricants that contain additives

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2053474A (en) * 1934-12-11 1936-09-08 Du Pont Higher alkyl borates and silicates and process for preparing same
US2129281A (en) * 1936-03-23 1938-09-06 Continental Oil Co Lubricating oils
US2242400A (en) * 1937-09-13 1941-05-20 Standard Oil Co Extreme pressure lubricant
US2274673A (en) * 1940-04-05 1942-03-03 Clarence E Earle Lubricating composition
US2403104A (en) * 1942-10-17 1946-07-02 Union Oil Co Lithium greases
US2446177A (en) * 1945-06-21 1948-08-03 George M Hain Silicone grease and method of preparation
US2450221A (en) * 1945-08-21 1948-09-28 Texas Co Shear-resistant grease
US2456642A (en) * 1946-08-13 1948-12-21 Robert L Merker Grease composition
US2486674A (en) * 1945-07-18 1949-11-01 Dow Chemical Co Lubricating grease
US2490691A (en) * 1946-10-03 1949-12-06 Du Pont Alkyl polysilicates
US2566365A (en) * 1946-06-15 1951-09-04 Minnesota Mining & Mfg Organic orthosilicates stable against hydrolysis

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2053474A (en) * 1934-12-11 1936-09-08 Du Pont Higher alkyl borates and silicates and process for preparing same
US2129281A (en) * 1936-03-23 1938-09-06 Continental Oil Co Lubricating oils
US2242400A (en) * 1937-09-13 1941-05-20 Standard Oil Co Extreme pressure lubricant
US2274673A (en) * 1940-04-05 1942-03-03 Clarence E Earle Lubricating composition
US2403104A (en) * 1942-10-17 1946-07-02 Union Oil Co Lithium greases
US2446177A (en) * 1945-06-21 1948-08-03 George M Hain Silicone grease and method of preparation
US2486674A (en) * 1945-07-18 1949-11-01 Dow Chemical Co Lubricating grease
US2450221A (en) * 1945-08-21 1948-09-28 Texas Co Shear-resistant grease
US2566365A (en) * 1946-06-15 1951-09-04 Minnesota Mining & Mfg Organic orthosilicates stable against hydrolysis
US2456642A (en) * 1946-08-13 1948-12-21 Robert L Merker Grease composition
US2490691A (en) * 1946-10-03 1949-12-06 Du Pont Alkyl polysilicates

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3091590A (en) * 1953-08-28 1963-05-28 California Research Corp Hydraulic fluid composition
US2990367A (en) * 1954-06-21 1961-06-27 Philipp Corp Clay-bodied lubricant containing a silicate ester
US3019191A (en) * 1954-09-28 1962-01-30 California Research Corp Stabilized hydraulic fluid composition
US2960474A (en) * 1957-05-20 1960-11-15 California Research Corp Silicate-silicone hydraulic fluid composition
US3146206A (en) * 1962-07-18 1964-08-25 California Research Corp Organosilicon fluid composition
US3350307A (en) * 1964-05-15 1967-10-31 Murex Welding Processes Ltd Lubricating greases
DE1750230A1 (en) * 1968-04-10 1972-04-06 Freudenberg Carl Fa Process to improve the sealing effect of radial sealing rings against lubricants that contain additives

Also Published As

Publication number Publication date
GB706033A (en) 1954-03-24

Similar Documents

Publication Publication Date Title
US3115465A (en) Stabilized compositions of matter
US2091627A (en) Composition of matter and process
US2497521A (en) Oil compositions containing amine salts of boro-diol complexes
GB565333A (en) Improvements relating to high temperature lubrication
US2651616A (en) Lithium hydroxy stearate grease compositions
US2681313A (en) Alkyl orthosilicate and alkoxysiloxane base grease compositions
US2848417A (en) Extreme high temperature grease compositions
US2606153A (en) Silicone greases
US3267031A (en) Stabilized silicone fluids
US3115466A (en) Synergistic antioxidants
US3156728A (en) Thiobis (2, 6-dialkylaniline) compounds
US2456642A (en) Grease composition
US2398173A (en) Lithium soap greases
US2971913A (en) Synithetic lubricant compositions
US3418348A (en) Phenyl titanium esters and preparations thereof
US3071549A (en) Preservative-type functional fluids
US2264353A (en) Lubricant
US3224972A (en) Stabilization with a 4,4'-thiobis (2,6-dialkylaniline)
US2652364A (en) High-temperature grease compositions
USRE22299E (en) Lubricating composition
US2293052A (en) Lubricant containing a lithium compound
US3780145A (en) Triphenyl phosphates
US2491028A (en) Lubricating grease compositions
US2274676A (en) Lubricant containing lithium salts
US2450321A (en) Rust-inhibiting greases