US3637497A - Moisture resistant dry film lubricants - Google Patents

Moisture resistant dry film lubricants Download PDF

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US3637497A
US3637497A US736287A US3637497DA US3637497A US 3637497 A US3637497 A US 3637497A US 736287 A US736287 A US 736287A US 3637497D A US3637497D A US 3637497DA US 3637497 A US3637497 A US 3637497A
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lubricant
dry film
coating
lubricants
film
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Vincent G Fitz Simmons
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    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16HGEARING
    • F16H57/00General details of gearing
    • F16H57/04Features relating to lubrication or cooling or heating
    • F16H57/041Coatings or solid lubricants, e.g. antiseize layers or pastes
    • 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
    • C10M2201/06Metal compounds
    • C10M2201/065Sulfides; Selenides; Tellurides
    • C10M2201/066Molybdenum sulfide
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/022Ethene
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/024Propene
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/14Synthetic waxes, e.g. polythene waxes
    • 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
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated 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
    • C10M2213/00Organic macromolecular compounds containing halogen 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
    • C10M2213/00Organic macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2213/02Organic macromolecular compounds containing halogen as ingredients in lubricant compositions obtained from monomers containing carbon, hydrogen and halogen only
    • 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
    • C10M2213/00Organic macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2213/04Organic macromolecular compounds containing halogen as ingredients in lubricant compositions obtained from monomers containing carbon, hydrogen, halogen and oxygen
    • 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
    • C10M2213/00Organic macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2213/06Perfluoro polymers
    • 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
    • C10M2213/00Organic macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2213/06Perfluoro polymers
    • C10M2213/062Polytetrafluoroethylene [PTFE]
    • 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
    • C10M2229/051Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon containing halogen
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/06Instruments or other precision apparatus, e.g. damping fluids
    • 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
    • C10N2050/04Aerosols
    • 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

  • the present invention relates generally to improvements in dry film lamellar lubricant coatings and bearings and more particularly pertains to protecting metals contacting these lubricants from corrosion, caused by the lubricant, without sacrificing lubrication properties.
  • the lubricant is covered with a thin coating having a melting point between 100 and 325 C., and a critical surface tension of 3] dynes/cm. or lower which imparts hydrophobic properties to the hydrophilic lubricant.
  • lubricant film For many applications of solid lubrication, it is convenient to deposit or bond the lubricant film to a metal substrate.
  • Dispersions of graphite and molybdenum disulfide, in volatile fluids, are available commercially for forming films by spraying, dipping or brushing. Cohesion between individual lubricant particles and adhesion to the substrate is often improved by incorporating binders in the lubricant solvent dispersion.
  • the lamellar lubricants are often compacted into a solid mass that can be loaded against a wearing surface to transfer lubricant continuously.
  • This method has been used for lubrication of wheel flanges, cylinder pistons, bearings, gears and the like.
  • Binders such as polytetrafluoroethylene, thermoplastic and thermosetting resins, aluminum oxide, inorganic silicates, and ceramic compositions have been employed. These binders many times adversely affect the solid lubricant. For instance, ceramic binders must be fired at 500 C. to obtain adhesion while polytetrafluoroethylene binders require a 380 C. sintering temperature. At these temperatures materials will oxidize. For example, molybdenum disulfide oxidizes to a more abrasive material molybdenum trioxide. Furthermore, some metal substrates undergo serious deterioration of physical properties.
  • Polytetrafluoroethylene has been used alone as a thin film solid lubricant because of its very low coefficient of friction.
  • the difficulty in using polytetrafiuoroethylene is the difficulty of forming an adherent surface film.
  • the high temperature required to sinter the polymer 380 C. or better, cannot be used because of oxidation, metal fatigue, etc.
  • the polytetrafiuoroethylene tends to coat only on the surface of porous material and temperature changes tend to separate the film from its substrate.
  • liquid lubricants under frictional pressure, also generate hydrostatic pressure within the lamellar crystallinestructure of lubricants such as molybdenum disulfide, graphite, etc., and cause fracturing and disintegration. These liquid wax lubricants also reduce self healing of the dry film lubricant.
  • the general purpose of this invention is to provide a dry film lubricant or bearing with a coating which is resistant to the penetration of moisture and which does not appreciably influence lubricating properties or wearing properties of the lubricant.
  • the coated bearings of this invention are particularly useful at the higher operating temperature range of dry film, say C. and up. Use of'the coating of this invention results in at least an order of magnitude reduction in the corrosivity of the dry film lubricant material on metallic substrates and wearing parts.
  • the improved coated dry film lubricants of this invention have the advantages of providing lubrication at temperatures from 100 to 325 C. without contaminant wear, hydrostatic destruction, or thermal destruction of the coating.
  • An object of the present invention is to provide improved moisture resistant and temperature resistant coated dry film lubricants which reduce appreciably the corrosivity of dry film materials in the presence of moisture.
  • a further object of the invention is to provide a coated and partially impregnated dry film or bearing having improved wear resistance and operating life.
  • a still further object is to provide coated dry film lubricants and bearings which may be cured at temperatures which do not cause hydrolytic or thermalchanges of the lubricant.
  • a further object of this invention is to provide a dry film lubricant coating which prevents ice adhesion to the film when exposed to low temperature.
  • Still another object is to provide a coating which prevents abrasive contamination of hydrophilic dry lubricant films.
  • the invention pertains to the alteration of the high-surface energy of lamellar dry film particles through the use of hydrophobic, relatively stable coating applied to the finished lubricant, whether film or bearing.
  • a thin film of the coating is applied to the dry film lubricant or bearing and is caused to at least partially permeate its structure.
  • the film or bearing is rapidly heated to a temperature sufficient to diffuse the coating into the lamellar lubricant.
  • a temperature between 100 and 325 C. is sufficient with the temperature preferably maintained near the coatings melting point.
  • Coatings dissolved in volatile diluent solvent are merely applied to the lubricant at ambient temperature with the solvent subsequently allowed to evaporate.
  • the impregnation of the dry film or bearing produces low-surface energy and resistance to moisture and contamination without changing appreciably the frictional behavior of the dry film lamellar solid particles.
  • the coating is applied to any conventional precoated substrate or bearing containing lamellar particles such as graphite, molybdenum disulfide,*or the like.
  • the coating is applied by spray brush, dip coating, or the like. Sufficient coating is applied to at least partially impregnate the lubricant and to coat the surface of the lubricant,
  • Useful coatings are those materials which are hydrophobic, not easily hydrolyzed or thermally degraded, and which have a melting point between 100 and 325 C. and a critical surface tension of 31 dynes/cm. or lower (20 C.).
  • Examples are: polymerized olefins such as polyethylene, polypropylene or the like; polymerized fluoro-olefins such as poly(vinyl fluoride), poly(vinylidene fluoride) or the like; polyfiuorosiloxanes such as X z) n S i- O) I where; R is lower alkyl for example methyl, hexyl, etc., or aryl such as phenyl, X is perfluoroalkyl or omega hydro perfluoroalkyl having one to 12 carbons, n is at least two, and z is l-2,000; polytetrafluoroethylene telomers, dispersed in solvent, and polyfiuor
  • Suitable polytetrafluoroethylene telomers are described in US. Pat. No. 3,067,262 to Brady. These polymers have an average molecular weight from 1,300 to 15,000, a crystalline melting point in the range 225 to 320 C. and a particle size from 0.01 to about 100 microns.
  • the polymers are commercially available in dispersion form in a suitable organic solvent such as trichlorotrifluoroethane or the like. These dispersions are available in concentration of 20 percent, percent or 2.5 percent and may further be diluted where desired. Concentrations ranging from 0.1 to 40 percent of fluorotelomer by weight dispersed in the organic solvent may be employed for coating purposes.
  • the preferred telomer has an average molecular weight of 3,700, a crystalline melting point of 300 C., a softening point of 265 C. and an approximate average particle size of 5 microns;
  • Such polymers are available from the DuPont Company under the trade name Vydax.
  • Particularly preferred coatings are the acrylate-type polymers used inthe textile industry for producing water repellent and dirt repellent fabrics. These materials are preferred because a low-critical surface tension, about dynes/cm. ease of application at ambient temperature, and thermal and hydrolytic stability. These polymers are prepared from acrylate-type esters and have the general formula:
  • R is a hydrogen or methyl
  • n is an integer from 1 to 12
  • m is an integer from 1 to l2
  • x is hydrogen or fluorine v specific examples of these esters are: 1H, ll-l, 2H- difiuoroethyl acrylate, 1H,. 1 H-trifluoroethyl methacrylate,
  • acrylate-type esters are readily polymerized by methods known to the art, for example, bulk polymerization, solution polymerization and emulsion polymerization, using catalysts such as benzoyl peroxide or other free radical initiators of polymerization.
  • catalysts such as benzoyl peroxide or other free radical initiators of polymerization.
  • a solution of from 0.1 to 40 percent polymer in volatile organic solvent may be used.
  • About 2 percent by weight polymer is preferred for coatingsl
  • the coating compositions of this invention. may
  • lamellar lubricant film or bearing For example, in dealing with dispersed polytetrafluoroethylene telomers, heating softeris the telomer and allows it to flow into the pore structure of the lamellar solids and also causes the evaporation of a solvent.
  • a solution of coating in volatile solvent for example, an acrylate-type polymer dispersed in xylene hexafluoride
  • the solvent is merely evaporated at room temperature to leave an adherent coating.
  • Ambient temperature application of the coatings is particularly useful where the temperature required to soften or melt a dispersed coating would cause thermal destruction of certain plastic binders used in dry film bearings.
  • the resulting coating applied to the dry film lubricant coated metal substrate or bearing is relatively cohesive and adherent film which is resistant to moisture and other contaminates of the atmosphere.
  • the films provide excellent corrosion inhibiting properties and further aid the lubricating ability of the graphite, molybdenum disulfide 'or other dry film lubricant.
  • the invention is illustrated, but not limited, by the following 4 EXAMPLE r
  • a polytetrafluoroethylene telomer having an average molecular weight of 3,700, crystalline melting weightof 300 C. and concentration of 2.5 percent fluorotelomer in inert trichlorotrifluoroethane is sprayed from an aerosol container onto a dry film of molybdenum disulfide dispersed in boehmite alumina binder and bonded to a steel substrate. The entire surface area of the film is coated. The coated lubricant is then heated to at least 265 C. to soften and diffuse the fluorotelomer into the lamellar lubricant film. The coated film is maintained at elevated temperature until the solvent vehicle is evaporated.
  • the temperature may be lowered and vacuum technique or other equivalent used to remove residual solvent.
  • the coating is sufiicient to prevent corrosion of the molybdenum disulfide coated steel for more than 24 hours whereas a control, without coating, corrodes within l hour.
  • EXAMPLE 2 A 2 percent solution of 1H, 1 H-pentadecafluorooctyl methacylate polymer dissolved in xylene hexafluoride is brushed on a cured lamellar coating of molybdenum disulfide supported on a steel plate. Sufficient material is used to coat the entire surface. The coated article is air dried to remove solvent. The coating is sufficient to prevent water corrosion of the molybdenum disulfide coated steel for more than 24 hours whereas a control, uncoated molybdenum disulfide plate, is corroded in less than 1 hour.
  • EXAMPLE 3 The timing clock is lubricated with a mixture of graphite and molybdenum disulfide in equal parts. Another similarly lubricated clocks lubricant is spray coated as in example 2.
  • the control, or uncoated device is inoperable below 40 F. at 65 percent relative humidity even when oil is used to reduce moisture sensitivity.
  • the coated timing device is operable below 0 F. at the same humidity conditions.
  • the improved coated lamellar dry films of this invention provide equivalent or better lubrication than prior dry films without exhibiting the corrosive nature of conventional dry films.
  • the coating provides added resistance to moisture corrosion, contamination by dirt and other substances contained in the environment, and prevents adhesion of ice to the lubricant at low temperature.
  • the coatings do not require excessive sintering temperatures, experienced for polytetrafiuoroethylene, and therefore allow a greater number of binder materials to be used to form solid bearings of dry film lubricant and binder.
  • the coatings also avoid the problems encountered using oils, greases and waxes in connection with lamellar solids since they do not significantly affect the durability or life of the coated dry film lubricant or bearing.
  • R is selected from the group consisting of hydrogen and methyl
  • n is an integer from one to 12
  • m is an integer from one to 12
  • X is selected from the group consisting of hydrogen and fluorine.

Abstract

Chemical and galvanic corrosion of metallic substrates, by dry film lubricants, is prevented by application over the lubricant surface of a hydrophobic organic polymer coating having a melting point between 100* to 325* C. and a critical surface tension of 31 dynes/cm. or lower.

Description

United States Patent Fitz Simmons [4 1 Jan. 25, 1972 MOISTURE RESISTANT DRY FILM LUBRICANTS Inventor: Vincent G. Fitz Simmons, Great Falls, Va.
Assignee: The United States of America as represented by the Secretary of the Navy Filed: June 12, 1968 Appl. No.: 736,287
US. Cl ..252/29, 252/12, 252/25, 252/54.6, 252/396 Int. Cl ..Cl0m 7/24, ClOm 7/06, ClOm 7/04 Field of Search ..252/l2.2, 12, 25, 29, 54.6, 252/396 Primary ExaminerDaniel E. Wyman Assistant Examinerl. Vaughn Attorney-R. S. Sciascia and A. L. Branning [57] ABSTRACT Chemical and galvanic corrosion of metallic substrates, by dry film lubricants, is prevented by application over the lubricant surface of a hydrophobic organic polymer coating having a melting point between 100 to 325 C. and a critical surface tension of31 dynes/cm. or lower.
2 Claims, No Drawings MOISTURE RESISTANT DRY FILM LUBRICANTS BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates generally to improvements in dry film lamellar lubricant coatings and bearings and more particularly pertains to protecting metals contacting these lubricants from corrosion, caused by the lubricant, without sacrificing lubrication properties. The lubricant is covered with a thin coating having a melting point between 100 and 325 C., and a critical surface tension of 3] dynes/cm. or lower which imparts hydrophobic properties to the hydrophilic lubricant.
2. Description of the Prior Art In the field of lamellar'dry film lubricants, it has been the general practice to employ layer-lattice materials such as graphite, M08 Cdl CdCl,, W8 CoCl Boron nitride, hydroxides and halides of divalent metals, and sulfides, selenides and tellurides of tetravalent metals, or the like, as dry lubricants to prevent metal wear. Of these, molybdenum disulfide and graphite are most commonly used.
For many applications of solid lubrication, it is convenient to deposit or bond the lubricant film to a metal substrate. Dispersions of graphite and molybdenum disulfide, in volatile fluids, are available commercially for forming films by spraying, dipping or brushing. Cohesion between individual lubricant particles and adhesion to the substrate is often improved by incorporating binders in the lubricant solvent dispersion.
In addition to placing dry films directly on the metal part, the lamellar lubricants are often compacted into a solid mass that can be loaded against a wearing surface to transfer lubricant continuously. This method has been used for lubrication of wheel flanges, cylinder pistons, bearings, gears and the like. Binders such as polytetrafluoroethylene, thermoplastic and thermosetting resins, aluminum oxide, inorganic silicates, and ceramic compositions have been employed. These binders many times adversely affect the solid lubricant. For instance, ceramic binders must be fired at 500 C. to obtain adhesion while polytetrafluoroethylene binders require a 380 C. sintering temperature. At these temperatures materials will oxidize. For example, molybdenum disulfide oxidizes to a more abrasive material molybdenum trioxide. Furthermore, some metal substrates undergo serious deterioration of physical properties.
Polytetrafluoroethylene has been used alone as a thin film solid lubricant because of its very low coefficient of friction. The difficulty in using polytetrafiuoroethylene is the difficulty of forming an adherent surface film. Also, for many applications, the high temperature required to sinter the polymer, 380 C. or better, cannot be used because of oxidation, metal fatigue, etc. Furthermore, the polytetrafiuoroethylene tends to coat only on the surface of porous material and temperature changes tend to separate the film from its substrate.
Surface films of polytetrafluoroethylene have been suggested by LeBrasse et al. U.S. Pat. No. 3,305,325, for coating composite bearing materials containing molybdenum disulfide in plastic binder to improve the bearings antifrictional characteristics during break in. Lubrication is obtained solely due to the polytetrailuoroethylene and not from the dry film lubricant. This application is severely limited by the high-sintering temperature required which decomposes most binders and by the tendency of the polyetrafiuoroethylene to coat the surface only, failing to penetrate into the pores of the bearing. The high-sintering temperature required to fuse polytetrafluoroethylene in effect prevents the use of most plastic-type binders used to produce dry film lubricant and bearings.
A major problem in using inorganic metallic lubricant compounds and graphite, as dry film lubricants, is the tendency of the lubricant to cause corrosion in the presence of moisture. DiSapio, U.S. Pat. No. 3,281,362 suggests forming a wax film over M08 particles to prevent corrosion. Waxes having melting points below 65 C. and having fair lubricant properties are employed. However, the use of oils, greases, and waxes in conjunction with lamellar solids cause significant loss in the durability or life of such dry film lubricants. Over a large portion of the normal operating temperatureof dry film bearings, above 60 C., waxes and the like are in a liquid state and act as vehicles for wear debris and contaminants while promoting wear much like lapping compounds. These liquid lubricants, under frictional pressure, also generate hydrostatic pressure within the lamellar crystallinestructure of lubricants such as molybdenum disulfide, graphite, etc., and cause fracturing and disintegration. These liquid wax lubricants also reduce self healing of the dry film lubricant.
SUMMARY OF Tris INVENTION The general purpose of this invention is to provide a dry film lubricant or bearing with a coating which is resistant to the penetration of moisture and which does not appreciably influence lubricating properties or wearing properties of the lubricant. The coated bearings of this invention are particularly useful at the higher operating temperature range of dry film, say C. and up. Use of'the coating of this invention results in at least an order of magnitude reduction in the corrosivity of the dry film lubricant material on metallic substrates and wearing parts. The improved coated dry film lubricants of this invention have the advantages of providing lubrication at temperatures from 100 to 325 C. without contaminant wear, hydrostatic destruction, or thermal destruction of the coating. The coatings penetrate the lubricant material itself or the bearing to give imp'roved lubricant adhesiveness and provide a moisture barrierfat least twice as good as that heretofore obtained. An object of the present invention is to provide improved moisture resistant and temperature resistant coated dry film lubricants which reduce appreciably the corrosivity of dry film materials in the presence of moisture.
A further object of the invention is to provide a coated and partially impregnated dry film or bearing having improved wear resistance and operating life.
A still further object is to provide coated dry film lubricants and bearings which may be cured at temperatures which do not cause hydrolytic or thermalchanges of the lubricant.
A further object of this invention is to provide a dry film lubricant coating which prevents ice adhesion to the film when exposed to low temperature.
Still another object is to provide a coating which prevents abrasive contamination of hydrophilic dry lubricant films.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The invention pertains to the alteration of the high-surface energy of lamellar dry film particles through the use of hydrophobic, relatively stable coating applied to the finished lubricant, whether film or bearing. A thin film of the coating is applied to the dry film lubricant or bearing and is caused to at least partially permeate its structure. For coatings dispersed in a diluent the film or bearing is rapidly heated to a temperature sufficient to diffuse the coating into the lamellar lubricant. A temperature between 100 and 325 C. is sufficient with the temperature preferably maintained near the coatings melting point. Coatings dissolved in volatile diluent solvent are merely applied to the lubricant at ambient temperature with the solvent subsequently allowed to evaporate. The impregnation of the dry film or bearing produces low-surface energy and resistance to moisture and contamination without changing appreciably the frictional behavior of the dry film lamellar solid particles.
The coating is applied to any conventional precoated substrate or bearing containing lamellar particles such as graphite, molybdenum disulfide,*or the like. The coating is applied by spray brush, dip coating, or the like. Sufficient coating is applied to at least partially impregnate the lubricant and to coat the surface of the lubricant,
Useful coatings are those materials which are hydrophobic, not easily hydrolyzed or thermally degraded, and which have a melting point between 100 and 325 C. and a critical surface tension of 31 dynes/cm. or lower (20 C.). Examples are: polymerized olefins such as polyethylene, polypropylene or the like; polymerized fluoro-olefins such as poly(vinyl fluoride), poly(vinylidene fluoride) or the like; polyfiuorosiloxanes such as X z) n S i- O) I where; R is lower alkyl for example methyl, hexyl, etc., or aryl such as phenyl, X is perfluoroalkyl or omega hydro perfluoroalkyl having one to 12 carbons, n is at least two, and z is l-2,000; polytetrafluoroethylene telomers, dispersed in solvent, and polyfiuoroacrylate-type polymers dissolved in solvent. Particularly preferred are the polytetrafiuoroethylene telomers and the polyfiuoroacrylate type polymers.
Suitable polytetrafluoroethylene telomers are described in US. Pat. No. 3,067,262 to Brady. These polymers have an average molecular weight from 1,300 to 15,000, a crystalline melting point in the range 225 to 320 C. and a particle size from 0.01 to about 100 microns. The polymers are commercially available in dispersion form in a suitable organic solvent such as trichlorotrifluoroethane or the like. These dispersions are available in concentration of 20 percent, percent or 2.5 percent and may further be diluted where desired. Concentrations ranging from 0.1 to 40 percent of fluorotelomer by weight dispersed in the organic solvent may be employed for coating purposes. It has been found that a 2 percent dispersion by weight of the polymer particles is very satisfactory. The preferred telomer has an average molecular weight of 3,700, a crystalline melting point of 300 C., a softening point of 265 C. and an approximate average particle size of 5 microns;
Such polymers are available from the DuPont Company under the trade name Vydax.
Particularly preferred coatings are the acrylate-type polymers used inthe textile industry for producing water repellent and dirt repellent fabrics. These materials are preferred because a low-critical surface tension, about dynes/cm. ease of application at ambient temperature, and thermal and hydrolytic stability. These polymers are prepared from acrylate-type esters and have the general formula:
where R is a hydrogen or methyl n is an integer from 1 to 12 m is an integer from 1 to l2 x is hydrogen or fluorine v specific examples of these esters are: 1H, ll-l, 2H- difiuoroethyl acrylate, 1H,. 1 H-trifluoroethyl methacrylate,
lH, lH-pentafluoropropyl u acrylate,]H, 1H, 3H- tetrafluoropropyl methacrylate, 1H, lH, 2H, ZH-pentafluorobutyl acrylate, 1H, 1H, SH-octafluoropentyl The acrylate-type esters are readily polymerized by methods known to the art, for example, bulk polymerization, solution polymerization and emulsion polymerization, using catalysts such as benzoyl peroxide or other free radical initiators of polymerization. For coating purposes a solution of from 0.1 to 40 percent polymer in volatile organic solvent may be used. About 2 percent by weight polymer is preferred for coatingsl The coating compositions of this invention. may
lamellar lubricant film or bearing. For example, in dealing with dispersed polytetrafluoroethylene telomers, heating softeris the telomer and allows it to flow into the pore structure of the lamellar solids and also causes the evaporation of a solvent. Where a solution of coating in volatile solvent is employed, for example, an acrylate-type polymer dispersed in xylene hexafluoride, the solvent is merely evaporated at room temperature to leave an adherent coating. Ambient temperature application of the coatings is particularly useful where the temperature required to soften or melt a dispersed coating would cause thermal destruction of certain plastic binders used in dry film bearings. The resulting coating applied to the dry film lubricant coated metal substrate or bearing is relatively cohesive and adherent film which is resistant to moisture and other contaminates of the atmosphere. The films provide excellent corrosion inhibiting properties and further aid the lubricating ability of the graphite, molybdenum disulfide 'or other dry film lubricant. I
The invention is illustrated, but not limited, by the following 4 EXAMPLE r A polytetrafluoroethylene telomer, having an average molecular weight of 3,700, crystalline melting weightof 300 C. and concentration of 2.5 percent fluorotelomer in inert trichlorotrifluoroethane is sprayed from an aerosol container onto a dry film of molybdenum disulfide dispersed in boehmite alumina binder and bonded to a steel substrate. The entire surface area of the film is coated. The coated lubricant is then heated to at least 265 C. to soften and diffuse the fluorotelomer into the lamellar lubricant film. The coated film is maintained at elevated temperature until the solvent vehicle is evaporated. Alternatively the temperature may be lowered and vacuum technique or other equivalent used to remove residual solvent. The coating is sufiicient to prevent corrosion of the molybdenum disulfide coated steel for more than 24 hours whereas a control, without coating, corrodes within l hour.
EXAMPLE 2 A 2 percent solution of 1H, 1 H-pentadecafluorooctyl methacylate polymer dissolved in xylene hexafluoride is brushed on a cured lamellar coating of molybdenum disulfide supported on a steel plate. Sufficient material is used to coat the entire surface. The coated article is air dried to remove solvent. The coating is sufficient to prevent water corrosion of the molybdenum disulfide coated steel for more than 24 hours whereas a control, uncoated molybdenum disulfide plate, is corroded in less than 1 hour.
EXAMPLE 3 The timing clock is lubricated with a mixture of graphite and molybdenum disulfide in equal parts. Another similarly lubricated clocks lubricant is spray coated as in example 2.
The control, or uncoated device, is inoperable below 40 F. at 65 percent relative humidity even when oil is used to reduce moisture sensitivity. The coated timing device is operable below 0 F. at the same humidity conditions.
The improved coated lamellar dry films of this invention provide equivalent or better lubrication than prior dry films without exhibiting the corrosive nature of conventional dry films. The coating provides added resistance to moisture corrosion, contamination by dirt and other substances contained in the environment, and prevents adhesion of ice to the lubricant at low temperature. The coatings do not require excessive sintering temperatures, experienced for polytetrafiuoroethylene, and therefore allow a greater number of binder materials to be used to form solid bearings of dry film lubricant and binder. The coatings also avoid the problems encountered using oils, greases and waxes in connection with lamellar solids since they do not significantly affect the durability or life of the coated dry film lubricant or bearing. Obviously many modifications and variations of the present invention are possible in the light of the above teaching. it is therefore to be understood that, within the scope of the appended claims the invention may be practiced wherein R is selected from the group consisting of hydrogen and methyl, n is an integer from one to 12, m is an integer from one to 12, and X is selected from the group consisting of hydrogen and fluorine. 2. The dry lubricant of claim 1 wherein said coating is 1H, lH-pentadecafluorooctyl methacrylate.

Claims (1)

  1. 2. The dry lubricant of claim 1 wherein said coating is 1H, 1H-pentadecafluorooctyl methacrylate.
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WO1979000075A1 (en) * 1977-07-29 1979-02-22 T Loran Cleaning and lubricating compositions
US4359798A (en) * 1977-07-29 1982-11-23 Loran T J System for cleaning and lubricating sound recording surfaces
JPS62161744A (en) * 1986-01-09 1987-07-17 Sony Corp Carboxylic acid perfluoroalkyl ester derivative and lubricant containing same
DE4407957A1 (en) * 1993-03-11 1994-11-24 Koyo Seiko Co Bearing arrangement
US5707035A (en) * 1994-08-31 1998-01-13 Hoover Universal, Inc. Vehicle seat adjuster
US20050229730A1 (en) * 2004-03-29 2005-10-20 Nissan Motor Co., Ltd. Slide apparatus for automotive vehicle
US20060286305A1 (en) * 2003-05-20 2006-12-21 Thies Jens Christoph J Hydrophobic coatings comprising reactive nano-particles
US20110094324A1 (en) * 2009-04-15 2011-04-28 Goodrich Actuation Systems Ltd. Actuator System
US20110187253A1 (en) * 2008-10-24 2011-08-04 Peter Jaehrling Fitting for household appliances and lubricant
US9366333B2 (en) * 2014-04-16 2016-06-14 Jtekt Corporation Vehicle differential gear

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US2628958A (en) * 1950-05-03 1953-02-17 Du Pont Polymerizable esters of alphamethylene carboxylic acids
GB712426A (en) * 1951-10-30 1954-07-21 Glacier Co Ltd Improvements in or relating to plain bearings
US3281362A (en) * 1963-01-25 1966-10-25 Dow Corning Wax-coated molybdenum disulfide
US3305325A (en) * 1964-10-21 1967-02-21 Federal Mogul Corp Bearing and method of making same

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2628958A (en) * 1950-05-03 1953-02-17 Du Pont Polymerizable esters of alphamethylene carboxylic acids
GB712426A (en) * 1951-10-30 1954-07-21 Glacier Co Ltd Improvements in or relating to plain bearings
US3281362A (en) * 1963-01-25 1966-10-25 Dow Corning Wax-coated molybdenum disulfide
US3305325A (en) * 1964-10-21 1967-02-21 Federal Mogul Corp Bearing and method of making same

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1979000075A1 (en) * 1977-07-29 1979-02-22 T Loran Cleaning and lubricating compositions
US4213870A (en) * 1977-07-29 1980-07-22 Loran T J Cleaning and lubricating compositions and method of using the same
US4359798A (en) * 1977-07-29 1982-11-23 Loran T J System for cleaning and lubricating sound recording surfaces
JPS62161744A (en) * 1986-01-09 1987-07-17 Sony Corp Carboxylic acid perfluoroalkyl ester derivative and lubricant containing same
JPH0714896B2 (en) 1986-01-09 1995-02-22 ソニー株式会社 Carboxylic acid perfluoroalkyl ester derivative and lubricant containing carboxylic acid perfluoroalkyl ester derivative
DE4407957A1 (en) * 1993-03-11 1994-11-24 Koyo Seiko Co Bearing arrangement
US5707035A (en) * 1994-08-31 1998-01-13 Hoover Universal, Inc. Vehicle seat adjuster
US20060286305A1 (en) * 2003-05-20 2006-12-21 Thies Jens Christoph J Hydrophobic coatings comprising reactive nano-particles
US20050229730A1 (en) * 2004-03-29 2005-10-20 Nissan Motor Co., Ltd. Slide apparatus for automotive vehicle
US9238932B2 (en) * 2004-03-29 2016-01-19 Nissan Motor Co., Ltd. Slide apparatus for automotive vehicle
US20110187253A1 (en) * 2008-10-24 2011-08-04 Peter Jaehrling Fitting for household appliances and lubricant
CN102165264A (en) * 2008-10-24 2011-08-24 保罗海蒂诗有限及两合公司 Fitting for household appliances and lubricant
JP2012506527A (en) * 2008-10-24 2012-03-15 ポール ヘティッヒ ゲーエムベーハー ウント ツェーオー. カーゲー Appliances and lubricants for household appliances
CN102165264B (en) * 2008-10-24 2014-03-19 保罗海蒂诗有限及两合公司 Fitting for household appliances and lubricant
US20110094324A1 (en) * 2009-04-15 2011-04-28 Goodrich Actuation Systems Ltd. Actuator System
EP2243946A3 (en) * 2009-04-15 2012-07-11 Goodrich Actuation Systems Ltd. Actuators system
US9366333B2 (en) * 2014-04-16 2016-06-14 Jtekt Corporation Vehicle differential gear

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