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US20030149136A1 - Aqueous coating agent for forming lubricating films - Google Patents

Aqueous coating agent for forming lubricating films Download PDF

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Publication number
US20030149136A1
US20030149136A1 US10/266,370 US26637002A US2003149136A1 US 20030149136 A1 US20030149136 A1 US 20030149136A1 US 26637002 A US26637002 A US 26637002A US 2003149136 A1 US2003149136 A1 US 2003149136A1
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resin
mos
aqueous coating
coating agent
agent
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US10/266,370
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Atsushi Ikezawa
Tetsuji Yamaguchi
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Priority claimed from JP10625996A external-priority patent/JPH09272884A/en
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/02Emulsion paints including aerosols
    • C09D5/024Emulsion paints including aerosols characterised by the additives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
    • 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
    • C10M111/00Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
    • C10M111/04Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
    • 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
    • C10M161/00Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a non-macromolecular compound, each of these compounds being essential
    • 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
    • C10M173/00Lubricating compositions containing more than 10% water
    • C10M173/02Lubricating compositions containing more than 10% water not containing mineral or fatty oils
    • 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
    • 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
    • C10M2201/0653Sulfides; Selenides; Tellurides used as base material
    • 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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/065Sulfides; Selenides; Tellurides
    • C10M2201/066Molybdenum sulfide
    • C10M2201/0663Molybdenum sulfide used as base material
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/04Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical
    • 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
    • C10M2209/04Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical
    • C10M2209/043Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical used as base material
    • 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
    • C10M2209/06Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
    • C10M2209/062Vinyl esters of saturated carboxylic or carbonic acids, e.g. vinyl acetate
    • 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
    • C10M2209/06Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
    • C10M2209/062Vinyl esters of saturated carboxylic or carbonic acids, e.g. vinyl acetate
    • C10M2209/0625Vinyl esters of saturated carboxylic or carbonic acids, e.g. vinyl acetate used as base material
    • 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/06Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
    • 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
    • C10N2050/01Emulsions, colloids, or micelles
    • 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
    • C10N2050/015Dispersions of solid lubricants
    • C10N2050/02Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating

Definitions

  • the present invention relates to an aqueous coating agent for forming lubricating films, in particular, to an aqueous coating agent for forming lubricating films suitable for prolonged use on sliding members of torque-transmitting parts utilized in automobile drive and prime mover systems.
  • Conventional aqueous coating agents for forming lubricating films comprise substances which possess excellent oil-proof and heat-resistant properties and are formed by dispersing molybdenum disulfide, graphite powder or carbon fibers in binders such as a polyimide resin, an epoxy resin, or a phenol resin.
  • the present invention is aimed at elimination of the problems of the prior art, and it is an object of the present invention to provide an aqueous coating agent for forming lubricating films with improved lubricating properties, long-service life, in particular, on sliding members of torque-transmitting parts utilized in automobile drive and prime mover systems, and excellent load-bearing properties.
  • the present invention is characterized by the fact that, in an aqueous coating agent for forming lubricating films, a number of specific solid lubricating agents is used in a specific weight ratio range, and that the aforementioned solid lubricating agents is used in a specific weight ratio with regard to a hydrophilic resin.
  • an aqueous coating agent for forming lubricating films that comprises the following first component, second component, and third component: the first component: a hydrophilic resin; the second component: a solid lubricating agent comprising MoS 2 and at least one antimony sulfide selected from the group consisting of Sb 2 S 3 and Sb 2 S 5 , where the weight ratio of MoS 2 to antimony sulfide is from 1:0.05 to 1:1.2; and the third component is water.
  • the weight ratio of the second component to the first component is from 0.7 to 3.
  • hydrophilic resin which is the aforementioned first component
  • hydrophilic organic resin What is meant here under by term “hydrophilic properties” is that the aforementioned organic resin is either soluble in water, or is at least stable in it in a dispersed form.
  • An organic resin with aforementioned hydrophilic properties is a resin which normally has in its molecule a hydrophilic polar group. The following are examples of hydrophilic polar groups:
  • organic resins which do not possess the aforementioned hydrophilic properties such as epoxy resins, alkyd resins, acrylic resins, and silicone resins, provided their hydrophilic properties have been improved.
  • Such an improvement can be achieved, e.g., by: (1) imparting hydrophilic properties as a result of graft polymerization or copolymerization of a monomer having a hydrophilic group capable of imparting hydrophilic properties to an organic resin which has no hydrophilic properties; or (2) introducing the hydrophilic group itself to an organic resin without hydrophilic properties as a result of amination, hydroxylation, carboxylation, or esterification.
  • an epoxy ester obtained by esterifying a hydroxyl group of an epoxy resin with linseed oil, dehydrated castor oil, soybean oil, and coconut oil, and the like.
  • the solid lubricating agent which is the aforementioned second component be represented by MoS 2 and at least one antimony sulfide selected from the group consisting of Sb 2 S 3 and Sb 2 S 5 , where the weight ratio of MoS 2 to antimony sulfide is from 1:0.05 to 1:1.2. If the solid lubricating agent component does not contain both the aforementioned antimony sulfide and MoS 2 , it would be impossible to obtain an aqueous coating agent for the formation of lubricating coating films with load-carrying capacity, which is an object of the present invention.
  • the solid lubricating agent of the second component may comprise more than one of the aforementioned antimony sulfide.
  • the aforementioned component contains both the antimony sulfide and MoS 2 but their weight ratio is beyond the range of 1:0.05 to 1:1.2, it would be still impossible to obtain an aqueous coating agent for the formation of lubricating coating films with properties specified by the present invention.
  • MoS 2 is used in an excessive amount, the period of time during which the coating film preserves its lubricating properties (i.e., the service life) will be shortened, and if the antimony sulfide is used in an excessive amount, the coating film will have insufficient load-bearing capacity, and will acquire an increased coefficient of friction.
  • a weight ratio of MoS 2 to antimony sulfide be from 1:0.2 to 1:0.5.
  • MoS 2 and antimony sulfide are indispensable components, but other solid lubricating agents also may be added provided their types and quantities are not detrimental to the object of the invention.
  • An example of such a solid lubricating agent is Sb 2 O 3 which is used in a weight ratio to the antimony sulfide which is from 1:0.5 to 1:5.0, preferably within the range of 1:0.5 to 1:1.5. The presence of this additive further improves lubricating properties.
  • Sb 2 O 3 in an excessive weight ratio beyond the specified range, on contrary, will decrease the service life of the lubricant.
  • a weight ratio of the second component to the first component i.e., the weight of the solid lubricating agent to the weight of the hydrophilic resin (hereinafter referred to as a “PB ratio”) should be from 0.7 to 3.
  • the most preferable PB ratio is within the range of 0.9 to 2.5.
  • the PB ratio is beyond the range of 0.7 to 3, e.g., if the solid lubricating agent is used in an excessive amount so that the aforementioned PB ratio exceeds 3, the strength of the coating film will be reduced and the service life of the lubricant will be shortened. Moreover, this will reduce anticorrosive properties to the level unsuitable for practical use. If, on the other hand, the hydrophilic resin is used in an excessive amount so that the PB ratio becomes lower than 0.7, it would be impossible to obtain a lubricating coating film with lubricating properties suitable for practical application.
  • an agent that improves compatibility of the hydrophilic resin for water can be added to the aqueous coating agent of the present invention for forming lubricating films.
  • the use of such an agent provides more efficient dissolving of the hydrophilic resin in water and stabilizes dispersion of this resin in water.
  • the use of such an agent broadens the assortment of types of hydrophilic resins suitable for the purposes of the present invention. As a result, e.g., less expensive hydrophilic resins can be selected.
  • the aforementioned compatibility agent may be represented by water-soluble amines, NaOH, or the like. A preferable one is ethanolamine. Nevertheless, there are no special limitations with regard to the type of the compatibility agent, provided it ensures compatibility of the hydrophilic resin used for the purposes of the present invention with water.
  • the aqueous coating agent of the present invention may be combined with other additives such as dyes, anti-corrosive agents, heat-resistance improvers, and the like. Furthermore, the aqueous coating agent of the present invention may be combined small amounts of graphite, tungsten disulfide, boron nitride, mica, or other solid lubricants, provided they are not detrimental to the effect of the invention.
  • the aqueous coating agent of the invention for forming lubricating films may be prepared by different methods. One example of these methods is given below.
  • the coating film used in the aforementioned experiment was obtained by drying an 8 to 13 ⁇ m thick coating film, formed by applying an appropriate coating agent, for 30 minutes at 25° C. with subsequent curing for 1 hour at 200° C.
  • Practical Examples 1-1, 1-3, 1-4, 1-5, and 1-6 show the effect exerted on the FALEX Endurance Life by the addition of at least one type of antimony sulfide selected from the group consisting of Sb 2 S 3 and Sb 2 S 5 .
  • Practical Example 1-2 shows an effect produced by adding Sb 2 O 3 to the aforementioned antimony sulfides.
  • MoS 2 is MoS 2 MF
  • Epoxy resin epoxy resin ester modified with linseed-oil and tung-oil: (RESYDROL WE 237L). “RESYDROL” is a registered trademark of Vianova-Kunstharz Aktiengesellschaft of Vienna.
  • MoS 2 MF [MoS 2 , Microfine], CLIMAX Co.
  • MoS 2 SF [MoS 2 , Superfine], CLIMAX Co.
  • MoDTP Molybdenum dithiophosphate
  • PTEF-1 Polytetrafluoroethylene powder
  • PTEF-2 Polytetrafluoroethylene dispersion
  • the invention is efficient in that it provides a coating agent which greatly reduces dissipation of organic solvents into environment and at the same time is capable of forming long-lasting lubricating films with perfect load-carrying capacity for use on sliding parts.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Dispersion Chemistry (AREA)
  • Lubricants (AREA)

Abstract

An aqueous coating agent comprising a hydrophilic resin; a solid lubricating agent comprising MoS2, antimony oxide, and at least one antimony sulfide selected from the group consisting of Sb2S3 and Sb2S5; and water; wherein the weight ratio of MoS2 to antimony sulfide is from 1:0.05 to 1:1.2 and the weight ratio of the solid lubricating agent to the hydrophilic resin is from 0.7:1 to 3:1.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • The present application is a division of application Ser. No. 08/826,305 filed Mar. 27, 1997, entitled “Aqueous Coating Agent for Forming Lubricating Film,” currently pending.[0001]
  • FIELD OF THE INVENTION
  • The present invention relates to an aqueous coating agent for forming lubricating films, in particular, to an aqueous coating agent for forming lubricating films suitable for prolonged use on sliding members of torque-transmitting parts utilized in automobile drive and prime mover systems. [0002]
  • BACKGROUND OF THE INVENTION
  • Conventional aqueous coating agents for forming lubricating films, in particular those for use with sliding parts, comprise substances which possess excellent oil-proof and heat-resistant properties and are formed by dispersing molybdenum disulfide, graphite powder or carbon fibers in binders such as a polyimide resin, an epoxy resin, or a phenol resin. [0003]
  • Although aforementioned coating agents for forming lubricating films in an aqueous-system form are known as well, in the majority of cases such coating agents are based on organic solvents. For example, in their earlier patent application (Japanese Laid-Open Patent Application Kokai 6-200275) the authors of the present patent application utilize an organic solvent. [0004]
  • Recently, however, more strict requirements were imposed concerning environment protection and reducing the impact on human health. For this reason, many industries had to quickly switch from organic solvent systems to aqueous systems. [0005]
  • For the same reason, there is a strong demand for aqueous systems exists also in the field of coating agents for forming lubricating films. An example of such a water-based coating agent for forming lubricating films is disclosed in Japanese Laid-Open Patent Application Kokai 7-11088 wherein silica is used as an agent for imparting lubricating properties. However, this aqueous coating agent for forming lubricating films appears to be unsuitable for prolonged use on sliding members of torque-transmitting parts utilized in automobile drive and prime mover systems. [0006]
  • The present invention is aimed at elimination of the problems of the prior art, and it is an object of the present invention to provide an aqueous coating agent for forming lubricating films with improved lubricating properties, long-service life, in particular, on sliding members of torque-transmitting parts utilized in automobile drive and prime mover systems, and excellent load-bearing properties. [0007]
  • SUMMARY OF THE INVENTION
  • The present invention is characterized by the fact that, in an aqueous coating agent for forming lubricating films, a number of specific solid lubricating agents is used in a specific weight ratio range, and that the aforementioned solid lubricating agents is used in a specific weight ratio with regard to a hydrophilic resin. [0008]
  • In other words, the problems inherent in the prior art are solved by utilizing an aqueous coating agent for forming lubricating films that comprises the following first component, second component, and third component: the first component: a hydrophilic resin; the second component: a solid lubricating agent comprising MoS[0009] 2 and at least one antimony sulfide selected from the group consisting of Sb2S3 and Sb2S5, where the weight ratio of MoS2 to antimony sulfide is from 1:0.05 to 1:1.2; and the third component is water. The weight ratio of the second component to the first component is from 0.7 to 3.
  • DETAILED DESCRIPTION OF THE INVENTION
  • The invention will be further described with reference to practical embodiments. Although there are no special limitations with regard to the hydrophilic resin which is the aforementioned first component, it is recommended that it be a hydrophilic organic resin. What is meant here under by term “hydrophilic properties” is that the aforementioned organic resin is either soluble in water, or is at least stable in it in a dispersed form. An organic resin with aforementioned hydrophilic properties is a resin which normally has in its molecule a hydrophilic polar group. The following are examples of hydrophilic polar groups: [0010]
    Figure US20030149136A1-20030807-C00001
  • Furthermore, it is possible to utilize organic resins which do not possess the aforementioned hydrophilic properties, such as epoxy resins, alkyd resins, acrylic resins, and silicone resins, provided their hydrophilic properties have been improved. Such an improvement can be achieved, e.g., by: (1) imparting hydrophilic properties as a result of graft polymerization or copolymerization of a monomer having a hydrophilic group capable of imparting hydrophilic properties to an organic resin which has no hydrophilic properties; or (2) introducing the hydrophilic group itself to an organic resin without hydrophilic properties as a result of amination, hydroxylation, carboxylation, or esterification. Especially preferable is an epoxy ester obtained by esterifying a hydroxyl group of an epoxy resin with linseed oil, dehydrated castor oil, soybean oil, and coconut oil, and the like. [0011]
  • It is recommended that the solid lubricating agent which is the aforementioned second component be represented by MoS[0012] 2 and at least one antimony sulfide selected from the group consisting of Sb2S3 and Sb2S5, where the weight ratio of MoS2 to antimony sulfide is from 1:0.05 to 1:1.2. If the solid lubricating agent component does not contain both the aforementioned antimony sulfide and MoS2, it would be impossible to obtain an aqueous coating agent for the formation of lubricating coating films with load-carrying capacity, which is an object of the present invention. The solid lubricating agent of the second component may comprise more than one of the aforementioned antimony sulfide. Furthermore, even though the aforementioned component contains both the antimony sulfide and MoS2 but their weight ratio is beyond the range of 1:0.05 to 1:1.2, it would be still impossible to obtain an aqueous coating agent for the formation of lubricating coating films with properties specified by the present invention. For example, if MoS2 is used in an excessive amount, the period of time during which the coating film preserves its lubricating properties (i.e., the service life) will be shortened, and if the antimony sulfide is used in an excessive amount, the coating film will have insufficient load-bearing capacity, and will acquire an increased coefficient of friction. This, in turn, will lead to heating during the use, and finally to thermal decomposition of the coating film and to a decrease in its service life. For the above reasons, it is recommended that a weight ratio of MoS2 to antimony sulfide be from 1:0.2 to 1:0.5.
  • MoS[0013] 2 and antimony sulfide are indispensable components, but other solid lubricating agents also may be added provided their types and quantities are not detrimental to the object of the invention. An example of such a solid lubricating agent is Sb2O3 which is used in a weight ratio to the antimony sulfide which is from 1:0.5 to 1:5.0, preferably within the range of 1:0.5 to 1:1.5. The presence of this additive further improves lubricating properties. The use of aforementioned Sb2O3 in an excessive weight ratio beyond the specified range, on contrary, will decrease the service life of the lubricant.
  • A weight ratio of the second component to the first component, i.e., the weight of the solid lubricating agent to the weight of the hydrophilic resin (hereinafter referred to as a “PB ratio”) should be from 0.7 to 3. The most preferable PB ratio is within the range of 0.9 to 2.5. [0014]
  • If the PB ratio is beyond the range of 0.7 to 3, e.g., if the solid lubricating agent is used in an excessive amount so that the aforementioned PB ratio exceeds 3, the strength of the coating film will be reduced and the service life of the lubricant will be shortened. Moreover, this will reduce anticorrosive properties to the level unsuitable for practical use. If, on the other hand, the hydrophilic resin is used in an excessive amount so that the PB ratio becomes lower than 0.7, it would be impossible to obtain a lubricating coating film with lubricating properties suitable for practical application. [0015]
  • There are no special limitations with regard to the amount of water, which is the aforementioned third component, provided it is used within the range that ensures obtaining of the aqueous coating agent for the formation of lubricating films with characteristics that satisfy the object of the invention. [0016]
  • Furthermore, in order to improve compatibility between water and the aforementioned hydrophilic resin, an agent that improves compatibility of the hydrophilic resin for water can be added to the aqueous coating agent of the present invention for forming lubricating films. The use of such an agent provides more efficient dissolving of the hydrophilic resin in water and stabilizes dispersion of this resin in water. Moreover, the use of such an agent broadens the assortment of types of hydrophilic resins suitable for the purposes of the present invention. As a result, e.g., less expensive hydrophilic resins can be selected. The aforementioned compatibility agent may be represented by water-soluble amines, NaOH, or the like. A preferable one is ethanolamine. Nevertheless, there are no special limitations with regard to the type of the compatibility agent, provided it ensures compatibility of the hydrophilic resin used for the purposes of the present invention with water. [0017]
  • The aqueous coating agent of the present invention may be combined with other additives such as dyes, anti-corrosive agents, heat-resistance improvers, and the like. Furthermore, the aqueous coating agent of the present invention may be combined small amounts of graphite, tungsten disulfide, boron nitride, mica, or other solid lubricants, provided they are not detrimental to the effect of the invention. [0018]
  • The aqueous coating agent of the invention for forming lubricating films may be prepared by different methods. One example of these methods is given below. [0019]
  • (1) Water (total quantity), a hydrophilic resin (30% of the entire charge), and a compatibility agent (total quantity) are mixed and stirred, until the hydrophilic resin is dissolved in water. [0020]
  • (2) One third (1/3) of the total amount of solid lubricating agents and other additives are loaded and treated for 30 minutes in a mill. This operation is repeated three times until the entire quantity of the aforementioned components is loaded. [0021]
  • (3) The remainder of the entire amount of the hydrophilic resin is loaded, and the mixture is treated in a mill for 10 minutes. [0022]
  • EXAMPLES
  • The invention will be further described in detail with reference to practical and comparative examples. In the following practical and comparative examples, the FALEX Pin And Vee Block Test Machine was used. “FALEX” is a registered trademark of Bellwood. The outer surfaces of the pin and V-block of this machine were subjected to sand blasting, and after treating with a phosphoric acid Mn[0023] 3(PO4)2, the contact surface of the pin was coated by spraying with an appropriate coating agent. The coating was dried and cured by heating. The so-called Falex Endurance Life was then measured as a time till tearing or scoring on the surface of the solidified coating under the following contact-conditions: linear contact; frequency of rotation 290 rpm; sliding speed 0.096 m/sec; and compressive force 1000 Lbs.
  • The coating film used in the aforementioned experiment was obtained by drying an 8 to 13 μm thick coating film, formed by applying an appropriate coating agent, for 30 minutes at 25° C. with subsequent curing for 1 hour at 200° C. [0024]
  • Practical Example 1
  • In Practical Examples 1-1 to 1-6, the Falex Endurance Life was determined for aqueous coating agents suitable for forming lubricating films. Tests were carried out with the use of the aforementioned FALEX testers and the test procedure. The results are shown in Tables 1, 2, and 3. [0025]
  • Practical Examples 1-1, 1-3, 1-4, 1-5, and 1-6 show the effect exerted on the FALEX Endurance Life by the addition of at least one type of antimony sulfide selected from the group consisting of Sb[0026] 2S3 and Sb2S5. Practical Example 1-2 shows an effect produced by adding Sb2O3 to the aforementioned antimony sulfides.
  • As can be seen from the results of the tests given in Tables 1 to 4, the addition of at least one type of an antimony sulfide, selected from the group consisting of Sb[0027] 2S3 and Sb2S5, to a lubricating-film-forming coating composition consisting of a hydrophilic resin and MoS2, makes it possible to obtain a very high Falex Endurance Life.
  • In particular, the Falex Endurance Life was especially high with further addition of Sb[0028] 2O3 to the aforementioned antimony sulfides.
    TABLE 1
    Practical Examples 1-1 1-2 1-3
    Hydrophilic Epoxy resin 14.0 16.87 14.0 *1
    resin (dry Melamine 2.1 2.52 2.1 *2
    residue) resin
    MoS2 25.0 21.30 24 *3
    Antimony Sb2S3 8.0 2.8 8
    sulfide Sb2S5
    Water 49.7 42.7 43.3
    Antimony Sb2O3 2.8
    oxide
    Solvent Ethanol- 1.0 1.9 1.0
    amine
    Bentonite 0.3 0.3 0.3
  • [0029]
    TABLE 2
    Practical
    examples 1-1 1-2 1-3
    MoS2/ 1:0.32 1:0.13 1:0.33 *4
    antimony
    sulfide
    Solid lubricant 2.05 1.38 1.99
    /resin
    FALEX 340 460 340
    Endurance Life
    (min)
  • [0030]
    TABLE 3
    Practical Examples 1-4 1-5 1-6
    Hydrophilic Epoxy resin 14.0 14.0 14.0 *1
    resin (dry Melamine 2.1 2.52 2.1 *2
    residue) resin
    MoS2 24 24 24 *3
    Antimony Sb2S3 8.0 8
    sulfide Sb2S5 8
    Water 43.5 43.5 43.5
    Antimony Sb2O3
    oxide
    Solvent Ethanol- 1.0 1.0 1.0
    amine
    Bentonite 0.3 0.3 0.3
  • [0031]
    TABLE 4
    Practical
    examples 1-4 1-5 1-6
    MoS2/ 1:0.33 1:0.33 1:0.33 *4
    antimony
    sulfide
    Solid lubricant/ 1.99 1.99 1.99
    resin
    FALEX 430 320 310
    Endurance Life
    (min)
  • Type of Sb[0032] 2S3 in Practical Example 1:
  • 1-1: Sb[0033] 2S3 grade 3
  • 1-2: Sb[0034] 2S3 grade 3
  • 1-3: Sb[0035] 2S3 grade 3
  • 1-4: Sb[0036] 2S3 grade 5
  • 1-5: Sb[0037] 2S3 natural product
  • MoS[0038] 2 is MoS2 MF
  • Practical Example 2
  • The FALEX Endurance Life was determined by the same method as in Practical Example 1, with the exception that in Practical examples 2-1 to 2-1 1 the aqueous lubricating-film-forming agents were used with different weight ratios of solid lubricating agents to resins. The results are shown in Tables 5 to 8. [0039]
    TABLE 5
    Practical Examples 2-1 2-2 2-3
    Resin (dry Epoxy resin 26.7 22.9 20.0 *1
    residue)
    MoS2 24 24 24 *3
    Antimony Sb2S3 8 8 8
    sulfide
    Water 27.6 33.2 37.5
    Solvent Ethanol- 2.0 1.8 1.6
    amine
    Bentonite 0.3 0.3 0.3
    MoS2/Antimony sulfide 1:0.33 1:0.33 1:0.33 *4
    Solid lubricant/resin 1.2 1.4 1.6
    FALEX Endurance Life (min) 360 470 425
  • [0040]
    TABLE 6
    Practical Examples 2-4 2-5 2-6
    Resin (dry Epoxy resin 17.8 16.0 12.8 *1
    residue)
    MoS2 24 24 24 *3
    Antimony Sb2S3 8 8 8
    sulfide
    Water 40.9 43.6 48.4
    Solvent Ethanol- 1.4 1.2 1.0
    amine
    Bentonite 0.3 0.3 0.3
    MoS2/Antimony sulfide 1:0.33 1:0.33 1:0.33 *4
    Solid lubricant/resin 1.8 2.0 2.5
    FALEX Endurance Life (min) 370 340 375
  • [0041]
    TABLE 7
    Practical Examples 2-7 2-8 2-9
    Resin (dry Epoxy resin 26.7 22.9 20.0 *1
    residue)
    MoS2 24 24 24 *3
    Antimony Sb2S3 8 8 8
    sulfide
    Water 27.6 33.2 37.7
    Solvent Ethanol- 2.0 1.8 1.8
    amine
    Bentonite 0.3 0.3 0.3
    MoS2/Antimony sulfide 1:0.33 1:0.33 1:0.33 *4
    Solid lubricant/resin 1.2 1.4 1.6
    FALEX Endurance Life (min) 470 480 400
  • [0042]
    TABLE 8
    Practical Examples 2-10 2-11
    Resin (dry Epoxy resin 16.0 12.8 *1
    residue)
    MoS2 24 24 *3
    Antimony Sb2S3 8 8
    sulfide
    Water 43.2 48.0
    Solvent Ethanol- 1.6 1.4
    amine
    Bentonite 0.3 0.3
    MoS2/Antimony sulfide 1:0.33 1:0.33 *4
    Solid lubricant/resin 2.0 2.5
    FALEX Endurance Life (min) 430 430
  • Practical Example 3
  • The FALEX Endurance Life was determined by the same method as in Practical Example 1, with the exception that in Practical Examples 3-1 to 3-4 the aqueous lubricating-film-forming agents were used with different weight ratios of MoS[0043] 2 to Sb2S3. The results are shown in Tables 9 and 10.
    TABLE 9
    Practical Examples 3-1 3-2
    Resin (dry Epoxy resin 19.9 19.9 *1
    residue) Melamine 3.0 3.0 *2
    resin
    MoS2 28.8 25.6 *3
    Antimony Sb2S3 3.2 6.4
    sulfide
    Water 42.9 42.9
    Solvent Ethanol- 1.9 1.9
    amine
    Bentonite 0.3 0.3
    MoS2/Antimony sulfide 1:0.11 1:0.25 *4
    Solid lubricant/resin 1.4 1.4
    FALEX Endurance Life (min) 380 460
  • [0044]
    TABLE 10
    Practical Examples 3-3 3-4
    Resin (dry Epoxy resin 19.9 19.9 *1
    residue) Melamine 3.0 3.0 *2
    resin
    MoS2 24 22.4 *3
    Antimony Sb2S3 8.0 9.6
    sulfide
    Water 42.9 42.9
    Solvent Ethanol- 1.9 1.9
    amine
    Bentonite 0.3 0.3
    MoS2/Antimony sulfide 1:0.33 1:0.42 *4
    Solid lubricant/resin 1.4 1.4
    FALEX Endurance Life (min) 480 470
  • Practical Example 4
  • The FALEX Endurance Life was determined by the same method as in Practical Example 1, with the exception that in Practical Examples 4-1 and 4-2 the aqueous lubricating-film-forming agents were used with a phenol resin. The results are shown in Table 11. [0045]
    TABLE 11
    Practical Examples 4-1 4-2
    Resin (dry Epoxy resin 15. 8 20.8 *5
    residue)
    MoS2 22.8 22.8 *3
    Antimony Sb2S3 5.7 5.7
    sulfide
    Water 18.38 17.47
    Solvent Ethanol- 1.8 1.8
    amine
    Bentonite 0.3 0.3
    Solid lubricant/resin 1.80 1.37 *4
    MoS2/Antimony sulfide 1:0.23 1:0.23
    FALEX Endurance Life (min) 430 400
  • Comparative Example
  • The FALEX Endurance Life was determined by the same method as in Practical Examples, with the exception that in Comparative Examples 1 through 9 the aqueous lubricating-film-forming agents were used with properties that did not satisfy the requirements specified for the aqueous lubricating-film-forming agents of the present invention. The results of the tests for Comparative Examples 1 through 6 are shown in Tables 12 through 17. As can be seen from Tables 12 through 17, comparison, e.g., between Practical Examples 1, 2 and Comparative Examples 8, 9 emphasizes the meaning of a weight ratio of solid lubricants to water-soluble resins. Furthermore, it can be seen from Comparative Example 7 that mere replacement of antimony sulfide with Sb[0046] 2O3 is not sufficient for a satisfactory effect.
    TABLE 12
    Comparative Examples 1 2 3
    Resin (dry Epoxy resin 14.0 14.0 14.0 *1
    residue) Melamine 2.1 2.1 2.1 *2
    resin
    MoS2 15 5.0 24.0 *3
    MoDTP
    ZnS 5.0 2.7
    Ca3(PO4)2 5.0
    PTFE-2 1.88 0.6
    PTFE-1 15.0
    (1) 0.1
  • [0047]
    TABLE 13
    Comparative
    Examples 1 2 3
    Sb2O3 *3
    BN
    Water 55.72 62.6 55.2
    Solvent 1.0 1.0 1.0
    Bentonite 0.3 0.3 0.3
    Solid lubricant/ 1.67 1.24 1.70 *4
    resin
    FALEX Endurance 118 10 65
    Life (min)
  • [0048]
    TABLE 14
    Comparative Examples 4 5 6
    Resin (dry Epoxy resin 14.0 14.0 14.0 *1
    residue) Melamine 2.1 2.1 2.1 *2
    resin
    MoS2 9.5 9.5 24.0 *3
    MoDTP 1.0
    ZnS 2.5 2.5
    Ca3(PO4)2
    PTFE-2
    PTFE-1
    (1)
  • [0049]
    TABLE 15
    Comparative
    Examples 4 5 6
    Sb2O3 12.5 12.5 *3
    BN 10.0
    Water 58.1 57.1 48.6
    Solvent 1.0 1.0 1.0
    Bentonite 0.3 0.3 0.3
    Solid lubricant/ 1.52 1.58 2.11 *4
    resin
    FALEX 186 163 36
    Endurance Life
    (min)
  • [0050]
    TABLE 16
    Comparative Examples 7 8
    Resin (dry Epoxy resin 14.0 26.58 *1
    residue) Melamine 2.1 4.51 *2
    resin
    MoS2 24 12.35 *3
    Antimony Sb2S3 1.62
    sulfide Sb2S5
    Water 43.5 36.7
    Antimony Sb2O3 8.0 1.62
    oxide
    Solvent Ethanol- 1.0 3.0
    amine
    Bentonite 0.3 0.3
    (see note
    above!!!)
  • [0051]
    TABLE 17
    Comparative Examples 7 8
    MoS2/Antimony sulfide 1:0.13 *4
    Solid lubricant/resin 1.99 0.5
    FALEX Endurance Life 200 140
    (min)
  • The starting materials which have been used in aforementioned Practical and Comparative Examples are described in more detail below: [0052]
  • Epoxy resin (epoxy resin ester modified with linseed-oil and tung-oil): (RESYDROL WE 237L). “RESYDROL” is a registered trademark of Vianova-Kunstharz Aktiengesellschaft of Vienna. [0053]
  • Melamine resin (non-plasticized melamine resin): (RESYDROL WM 501) [0054]
  • MoS[0055] 2 MF: [MoS2, Microfine], CLIMAX Co.
  • MoS[0056] 2 SF: [MoS2, Superfine], CLIMAX Co.
  • Sb[0057] 2S3 grade 3: Product of synthesis of GESCHAFTSBEREICH-CHEMI Co., DBPC GRADE 3
  • Sb[0058] 2S3 grade 5: Product of synthesis GESCHAFTSBEREICH-CHEMI Co., DBPC GRADE5
  • Sb[0059] 2S3 N: natural product
  • Sb[0060] 2S5: product of GESCHAFTSBEREICH-CHEMI Co
  • Sb[0061] 2O3: product of LIEBAU CHEMIE HANDELSGESELSCHAFT GMBH.
  • [ANTIMONTRIOXIDE LCH/RS][0062]
  • MoDTP: Molybdenum dithiophosphate [0063]
  • PTEF-1: Polytetrafluoroethylene powder [0064]
  • PTEF-2: Polytetrafluoroethylene dispersion [0065]
  • The invention is efficient in that it provides a coating agent which greatly reduces dissipation of organic solvents into environment and at the same time is capable of forming long-lasting lubricating films with perfect load-carrying capacity for use on sliding parts. [0066]

Claims (7)

That which is claimed is:
1. An aqueous coating agent comprising:
a hydrophilic resin;
a solid lubricating agent comprising MoS2, antimony oxide, and at least one antimony sulfide selected from the group consisting of Sb2S3 and Sb2S5; and
water;
wherein the weight ratio of MoS2 to antimony sulfide is from 1:0.05 to 1:1.2 and the weight ratio of the solid lubricating agent to the hydrophilic resin is from 0.7:1 to 3:1.
2. The aqueous coating agent according to claim 1, wherein the weight ratio of antimony oxide to antimony sulfide is from 1:0.5 to 1:5.0.
3. The aqueous coating agent of claim 2, wherein the weight ratio of antimony sulfide is from 1:0.5 to 1:1.5.
4. The aqueous coating agent of claim 1, wherein said hydrophilic resin is an epoxy ester obtained by esterifying an epoxy resin with an aliphatic resin.
5. The aqueous coating agent of claim 1, further comprising a compatibility agent that improves compatibility between water and the hydrophilic resin.
6. The aqueous coating agent of claim 5, wherein the compatibility agent is selected from the group consisting of water soluble amines, NaOH and ethanolamine.
7. The aqueous coating agent of claim 6, wherein the compatibility agent is ethanolamine.
US10/266,370 1996-04-03 2002-10-07 Aqueous coating agent for forming lubricating films Abandoned US20030149136A1 (en)

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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US687715A (en) * 1901-03-28 1901-12-03 Alfred G Bayles Gas-regulator.
US3736276A (en) * 1970-11-06 1973-05-29 Canada Wire & Cable Co Ltd Electrocoating bath compositions
US3873458A (en) * 1973-05-18 1975-03-25 United States Steel Corp Resin-containing lubricant coatings
US3975322A (en) * 1974-09-30 1976-08-17 Westinghouse Electric Corporation Rapid drying epoxy resin ester
US4303537A (en) * 1978-11-15 1981-12-01 Dow Corning Gmbh Water based lubricant
US5432211A (en) * 1991-10-24 1995-07-11 Nihon Parkerizing Co., Ltd. Lubricating paint

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JP2983786B2 (en) 1992-12-25 1999-11-29 トヨタ自動車株式会社 Coating agent for forming lubricating film
JP3347823B2 (en) 1993-06-25 2002-11-20 旭硝子株式会社 Polytetrafluoroethylene granules
JPH0734030A (en) * 1993-07-20 1995-02-03 Dainippon Toryo Co Ltd Paint composition and coated aluminum material
CA2140117A1 (en) * 1994-06-09 1995-12-10 Hiroyuki Tanabe Coated aluminum material

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Publication number Priority date Publication date Assignee Title
US687715A (en) * 1901-03-28 1901-12-03 Alfred G Bayles Gas-regulator.
US3736276A (en) * 1970-11-06 1973-05-29 Canada Wire & Cable Co Ltd Electrocoating bath compositions
US3873458A (en) * 1973-05-18 1975-03-25 United States Steel Corp Resin-containing lubricant coatings
US3975322A (en) * 1974-09-30 1976-08-17 Westinghouse Electric Corporation Rapid drying epoxy resin ester
US4303537A (en) * 1978-11-15 1981-12-01 Dow Corning Gmbh Water based lubricant
US5432211A (en) * 1991-10-24 1995-07-11 Nihon Parkerizing Co., Ltd. Lubricating paint

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