(19)
(11) EP 2 824 167 B1

(12) EUROPEAN PATENT SPECIFICATION

(45) Mention of the grant of the patent:
08.08.2018 Bulletin 2018/32

(21) Application number: 13757298.8

(22) Date of filing: 01.03.2013
(51) International Patent Classification (IPC): 
C10M 169/06(2006.01)
C10N 20/02(2006.01)
C10N 40/02(2006.01)
C10N 50/10(2006.01)
C10M 169/00(2006.01)
C10N 30/06(2006.01)
C10N 40/04(2006.01)
C10N 20/06(2006.01)
(86) International application number:
PCT/JP2013/055624
(87) International publication number:
WO 2013/133149 (12.09.2013 Gazette 2013/37)

(54)

GREASE COMPOSITION

SCHMIERFETTZUSAMMENSETZUNG

COMPOSITION DE GRAISSE


(84) Designated Contracting States:
AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

(30) Priority: 05.03.2012 JP 2012047750

(43) Date of publication of application:
14.01.2015 Bulletin 2015/03

(73) Proprietor: JX Nippon Oil & Energy Corporation
Chiyoda-ku Tokyo 100-8162 (JP)

(72) Inventors:
  • AYAME, Yusuke
    Tokyo 100-8162 (JP)
  • SAKAI, Kazumi
    Tokyo 100-8162 (JP)
  • SHITARA, Yuji
    Tokyo 100-8162 (JP)

(74) Representative: Müller-Boré & Partner Patentanwälte PartG mbB 
Friedenheimer Brücke 21
80639 München
80639 München (DE)


(56) References cited: : 
EP-A1- 2 341 121
WO-A1-2006/114442
WO-A1-2010/079743
JP-A- 2008 231 293
JP-A- 2011 093 963
EP-A2- 2 000 524
WO-A1-2009/153938
JP-A- S58 154 800
JP-A- 2010 209 129
   
     
    Remarks:
    The file contains technical information submitted after the application was filed and not included in this specification
     
    Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention).


    Description

    Technical Field



    [0001] The invention relates to a grease composition that utilizes a urea-based thickener.

    Background Art



    [0002] Grease has been mainly used for slide bearings, rolling bearings, and sliding surfaces where it is difficult to maintain adhesion of a lubricant film due to the movement of the contact surface. In particular, urea-based grease that utilizes a urea-based thickener exhibits excellent water resistance, mechanical stability, and heat resistance, and has been widely used for metal-metal sliding parts at a low speed with a high load such as an automotive constant-velocity joint.

    [0003] A grease composition that comprises a base oil, an organomolybdenum compound (e.g., a molybdenum dialkyldithiocarbamate sulfide), a molybdenum disulfide, a zinc dithiophosphate compound, and an aliphatic amide has been proposed as a grease composition used for a constant-velocity joint (see PTL 1 to 3).

    [0004] However, the above grease composition is insufficient in terms of lubricity and particularly wear resistance, and shows a deterioration in wear resistance during long-term use at a high temperature. WO 2009/153938 A1 and JP2008231293 disclose lubricating compositions comprising an amide compound.

    Citation List


    Patent Literature



    [0005] 

    PTL 1: JP-A-2001-11481

    PTL 2: JP-A-2005-226038

    PTL 3: JP-A-2008-19288


    Summary of Invention


    Technical Problem



    [0006] An object of the invention is to provide a grease composition that exhibits excellent lubricity, in particular excellent wear resistance, and shows only a small extent of deterioration in wear resistance with long-term use at high temperatures.

    Solution to Problem



    [0007] The inventors of the invention conducted extensive studies in order to achieve the above object. As a result, the inventors found that, in comparison with a grease composition that is prepared by merely dispersing and mixing an amide compound powder into grease, a grease composition obtained by heating and melting an amide compound in the presence of a lubricant base oil forms a three-dimensional network structure of the amide holding the lubricant base oil therein to afford the grease composition significantly improved wear resistance and to show only a small extent of deterioration in wear resistance with long-term use under high temperatures.

    [0008] The invention was completed based on the above finding, and is set out in the appended set of claims.

    Advantageous Effects of Invention



    [0009] The grease composition according to the invention exhibits excellent water resistance, mechanical stability, and heat resistance, provides excellent wear resistance to metal-metal sliding parts at a low speed with a high load, and shows only a small extent of deterioration in wear resistance with long-term use under high temperatures.

    Description of Embodiments



    [0010] The grease composition according to the invention comprises a lubricant base oil, an amide compound, a solid lubricant, and a urea-based thickener.

    [Lubricant base oil]



    [0011] A mineral oil-based lubricant base oil or a synthetic lubricant base oil may be used as the lubricant base oil used in connection with the invention. It is preferable to use a lubricant base oil having a kinematic viscosity of 1 to 1000 mm2/s, and more preferably 20 to 300 mm2/s at 40°C. If the kinematic viscosity (at 40°C) of the lubricant base oil falls outside the range of 1 to 1000 mm2/s, it may be difficult to easily prepare a grease composition having the desired consistency.

    [0012] It is preferable to use a lubricant base oil having a density of 0.75 to 0.95 g/cm3 at 15°C since the dispersibility of the solid lubricant is improved. In order to prepare grease having excellent lubricity, it is preferable to use a lubricant base oil having a viscosity index of 90 or more (more preferably 95 to 250), a pour point of -10°C or less (more preferably -15 to -70°C), and a flash point of 150°C or more.

    [0013] Examples of the mineral oil-based lubricant base oil include lubricant fractions obtained by distilling crude oil under atmospheric pressure optionally followed by distillation under reduced pressure to obtain a distillate, and refining the distillate using various types of refining process. Examples of the refining process include hydrotreating, solvent extraction, solvent dewaxing, hydrodewaxing, washing with sulfuric acid, clay treatment, and the like. The base oil used in connection with the invention can be obtained by combining these processes in an appropriate order. A mixture of a plurality of refined oils having different properties is also useful, wherein the mixture is obtained by using different types of crude oils or distillates and by a different combination and/or order of processes. The base oil obtained by each method may preferably be used as long as the properties of the base oil are adjusted to fall within the above ranges.

    [0014] It is preferable to use a material that exhibits excellent hydrolytic stability as the synthetic lubricant base oil. The synthetic lubricant base oil is at least one selected from polyolefins such as a poly-α-olefin, a polybutene, and a copolymer of two or more olefins, polyesters, polyalkylene glycols, alkylbenzenes, alkylnaphthalenes, It is preferable to use a poly-α-olefin from the viewpoint of availability, cost, viscosity, oxidation stability, and compatibility with a system member. A polymer of 1-dodecene or 1-decene is more preferable as the poly-α-olefin from the viewpoint of cost.

    [0015] These synthetic lubricant base oils may be used either alone or in combination. The synthetic lubricant base oil may be used in combination with the mineral oil-based lubricant base oil.

    [0016] When using a mixture of a plurality of types of lubricant base oil including a synthetic lubricant base oil, the properties of each base oil are not necessary to fall within the above ranges as long as the base oil mixture satisfies the above properties. Therefore, each synthetic base oil need not necessarily satisfy the above properties, but it is preferable that the properties of each synthetic base oil fall within the above ranges.

    [0017] The content of the lubricant base oil in the grease composition is preferably 50 to 95 mass%, and more preferably 60 to 85 mass%, based on the total amount of the grease composition. If the content of the lubricant base oil is outside the range of 50 to 95 mass%, it may be difficult to easily prepare a grease composition having the desired consistency.

    [Amide compound]



    [0018] The amide compound used in connection with the invention is a monoamide that includes one amide group (-NH-CO-), a bisamide that includes two amide groups, or a triamide that includes three amide groups, The bisamide and the triamide have an advantage in that the frictional resistance in the sliding part can be reduced even when the amide compound is used in a relatively small amount.

    [0019] The bisamide may be an acid amide of a diamine or an acid amide of a diacid.

    [0020] It is preferable to use an amide compound having a melting point of 40 to 180°C (more preferably 80 to 180°C, and still more preferably 100 to 170°C) and a molecular weight of 242 to 932 (more preferably 298 to 876).

    [0021] The monoamide is represented by the following general formula (1), the bisamide is represented by the following general formulas (2) and (3), and the triamide is represented by the following general formula (4).

            R1-CO-NH-R2     (1)

            R1-CO-NH-A1-NH-CO-R2     (2)

            R1-NH-CO-A1-CO-NH-R2     (3)

            R1-M-A1-CH(A2-M-R3)-A3-M-R2     (4)

    wherein R1, R2, and R3 are independently a hydrocarbon group having 5 to 25 carbon atoms. The hydrocarbon group may be an aliphatic hydrocarbon group, an alicyclic hydrocarbon group, or an aromatic hydrocarbon group. R2 in the general formula (1) may be a hydrogen atom. A1, A2, and A3 are independently an aliphatic hydrocarbon group having 1 to 10 carbon atoms, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, or a divalent hydrocarbon group having 1 to 10 carbon atoms formed by combining these groups, and M is an amide group.

    [0022] It is preferable that R2 is a hydrogen atom or a saturated or unsaturated chain hydrocarbon group having 10 to 20 carbon atoms when the amide compound is the monoamide.

    [0023] It is preferable that A1 is a divalent saturated chain hydrocarbon group having 1 to 4 carbon atoms when the amide compound is the acid amide of a diamine.

    [0024] Some of the hydrogen atoms of the hydrocarbon group represented by R1, R2, or A1 in the general formulas (2) and (3) may be substituted with a hydroxyl group (-OH).

    [0025] An amide compound in which A1, A2, and A3 are an aliphatic hydrocarbon group is referred herein to as "aliphatic amide", an amide compound in which at least one of A1, A2, and A3 is an aromatic hydrocarbon group is referred herein to as "aromatic amide", and an amide compound in which at least one of A1, A2, and A3 is an alicyclic hydrocarbon group or an aromatic hydrocarbon group is referred herein to as "non-aliphatic amide".

    [0026] It is preferable that R1, R2, and R3 is a saturated or unsaturated chain hydrocarbon group having 10 to 20 carbon atoms when the amide compound is the aliphatic amide.

    [0027] It is preferable that R1, R2, and R3 is a saturated or unsaturated chain hydrocarbon group having 10 to 20 carbon atoms or an aromatic hydrocarbon group when the amide compound is the aromatic amide.

    [0028] The non-aliphatic amide may also be used as the amide compound, but it is preferable to use the aliphatic amide as the amide compound. It is preferable that A1 is a divalent saturated chain hydrocarbon group having 1 to 4 carbon atoms when the amide compound is the acid amide of a diamine (general formula (3)).

    [0029] Specific examples of the monoamide include saturated fatty acid amides such as lauric acid amide, palmitic acid amide, stearic acid amide, behenic acid amide, and hydroxystearic acid amide, unsaturated fatty acid amides such as oleic acid amide and erucic acid amide, substituted amides of a saturated or unsaturated long-chain fatty acid and a long-chain amine such as stearylstearic acid amide, oleyloleic acid amide, oleylstearic acid amide, and stearyloleic acid amide, and the like.

    [0030] Specific examples of the acid amide of a diamine represented by the general formula (2) include ethylene bis-stearic acid amide, ethylene bis-isostearic acid amide, ethylene bis-oleic acid amide, methylene bis-lauric acid amide, hexamethylene bis-oleic acid amide, hexamethylene bis-hydroxystearic acid amide, and the like. Specific examples of the bisamide of a diacid represented by the general formula (3) include N,N'-bis-stearylsebacic acid amide and the like.

    [0031] Among these, the amide compounds represented by the general formula (2) or (3) in which R1 and R2 are independently a saturated chain hydrocarbon group or an unsaturated chain hydrocarbon group having 12 to 20 carbon atoms are preferable.

    [0032] There are various triamide compounds that are represented by the general formula (4). Specific examples of a compound among the compounds represented by the general formula (4) that can be suitably used in connection with the invention include an N-acylamino acid diamide compound. The N-acyl group included in the N-acylamino acid diamide compound is preferably a linear or branched saturated or unsaturated aliphatic acyl group having 1 to 30 carbon atoms, or an aromatic acyl group in particular, a caproyl group, a capryloyl group, a lauroyl group, a myristoyl group, or a stearoyl group. The amino acid included in the N-acylamino acid diamide compound is preferably aspartic acid or glutamic acid. The amine of the amide group included in the N-acylamino acid diamide compound is preferably a linear or branched saturated or unsaturated aliphatic amine having 1 to 30 carbon atoms, and more preferably butylamine, octylamine, laurylamine, isostearylamine, or stearylamine. In particular, N-lauroyl-L-glutamic acid-a,y-di-n-butylamide is preferable.

    [0033] These amide compounds may be used either alone or in combination. The content of the amide compound in the grease composition is 0.1 to 50 mass%, and preferably 3 to 35 mass%, based on the total amount of the grease composition.

    [Solid lubricant]



    [0034] The solid lubricant is a layered compound or a fluororesin due to excellent lubricity.

    [0035] A compound having a layered crystal structure is melamine cyanurate and boron nitride. Note that it is undesirable to use a compound that includes a heavy metal or sulfur from the viewpoint of environmental pollution and the like. The fluororesin is a polytetrafluoroethylene (PTFE).

    [0036] These solid lubricants may be used either alone or in combination. A solid lubricant having an appropriate particle size may be selected depending on the application. It is preferable to use a solid lubricant having a particle size (diameter) of 0.2 to 50 µm, and more preferably 1 to 10 µm.

    [0037] The content of the solid lubricant in the grease composition is 0.1 to 10 mass%, and preferably 0.2 to 5 mass%, based on the total amount of the grease composition.

    [Urea-based thickener]



    [0038] A diurea compound obtained by reacting a diisocyanate with a monoamine, a polyurea compound obtained by reacting a diisocyanate with a monoamine and a diamine, or the like may be used as the urea-based thickener.

    [0039] Examples of a preferable diisocyanate include phenylene diisocyanate, tolylene diisocyanate, diphenyl diisocyanate, diphenylmethane diisocyanate, octadecane diisocyanate, decane diisocyanate, hexane diisocyanate, and the like. Examples of a preferable monoamine include octylamine, dodecylamine, hexadecylamine, stearylamine, oleylamine, aniline, p-toluidine, cyclohexylamine, and the like. Examples of a preferable diamine include ethylenediamine, propanediamine, butanediamine, hexanediamine, octanediamine, phenylenediamine, tolylenediamine, xylenediamine, diaminodiphenylmethane, and the like.

    [0040] These urea-based thickeners may be used either alone or in combination. The content of the urea-based thickener in the grease composition may be appropriately determined as long as the desired consistency can be obtained. The content of the urea-based thickener in the grease composition is 2 to 30 mass%, and preferably 5 to 20 mass%, based on the total amount of the grease composition.

    [Additive]



    [0041] The grease composition according to the invention may optionally include a detergent, a dispersant, an antiwear agent, a viscosity index improver, an antioxidant, an extreme pressure agent, a rust-preventive agent, a corrosion inhibitor, and the like that are normally used for a lubricant or grease in addition to the above components.

    [Preparation method]



    [0042] The grease composition according to the invention may be prepared using a normal grease preparation method. A mixture comprising the amide compound is heated to a temperature equal to or higher than the melting point of the amide compound at least once, after mixing the amide compound.

    [0043] Specifically, the grease composition may be prepared by heating the amide compound and the lubricant base oil to a temperature equal to or higher than the melting point of the amide compound, cooling the mixture, and then physically mixing the cooled mixture with normal grease that comprises the solid lubricant, the thickener, and the lubricant base oil. Alternatively, all of the components including the urea-based thickener may be mixed, heated to a temperature equal to or higher than the melting point of the amide compound, and then cooled.

    [0044] When the amide compound is heated to a temperature equal to or higher than the melting point of the amide compound in the presence of at least the lubricant base oil, the lubricant base oil is held in a semi-solid gel state by the amide compound that forms a three-dimensional network structure, but freely moves within the network structure microscopically. This suggests that, when the gel-like composition having lubricity comes in contact with small voids formed in a porous material, the liquid lubricant base oil can move into the small voids from the gel due to a capillary phenomenon, or suggests that, when an excess liquid lubricant base oil is present in the system, the excess liquid lubricant base oil is incorporated in the gel due to a capillary phenomenon through the three-dimensional structure of the gel, for example. The urea-based thickener provides consistency in such a state. The grease composition thus exhibits excellent water resistance, mechanical stability, and heat resistance, provides excellent wear resistance, and shows only a small extent of deterioration in wear resistance with long-term use under high temperatures.

    Examples


    1. Lubricant base oil



    [0045] 
    1. (1) Mineral oil-based lubricant base oil
      • Lubricant base oil obtained by distilling atmospheric distillation residue under reduced pressure and subjecting the resulting distillate to solvent refining

        Kinematic viscosity at 40°C: 68 mm2/s

        Density at 15°C: 0.87 g/cm3

        Viscosity index: 100

        Pour point: -10°C

        Flash point: 250°C

    2. (2) Synthetic lubricant base oil

      Poly-α-olefin ("Durasyn 170" manufactured by INEOS)

      Kinematic viscosity at 40°C: 68 mm2/s

      Density at 15°C: 0.83 g/cm3

      Viscosity index: 133

      Pour point: -45°C

      Flash point: 250°C


    2. Amide compound


    2-1. Aliphatic amide



    [0046] 
    1. (1) Ethylene bis-stearic acid amide (special grade reagent)
    2. (2) Ethylene bis-oleic acid amide (special grade reagent)
    3. (3) Stearic acid monoamide (special grade reagent)

    2-2. Aromatic amide



    [0047] 
    1. (1) m-Xylylene bis-stearic acid amide (special grade reagent)

    3. Solid lubricant



    [0048] 
    1. (1) Melamine cyanulate (MCA, average particle size: 4 µm, "MELAPUR MC25" manufactured by BASF)
    2. (2) Polytetrafluoroethylene (PTFE, average particle size: 4 µm, "KTL-8N" manufactured by Kitamura Limited)
    3. (3) Boron nitride (average particle size: 2 µm, "HP-P1" manufactured by Mizushima Ferroalloy Co., Ltd.)


    [0049] The average particle size was measured by laser diffractometry.

    4. Urea-based thickener



    [0050] 
    1. (1) Aliphatic diurea obtained by reacting octadecylamine with methylenediphenyl diisocyanate
    2. (2) Alicyclic diurea obtained by reacting cyclohexylamine with methylenediphenyl diisocyanate
    3. (3) Aromatic diurea obtained by reacting p-toluidine with methylenediphenyl diisocyanate

    5. Additive



    [0051] Diphenylamine was added to each composition as an antioxidant.

    [Preparation method]



    [0052] Each component was charged in a vessel in the amount (wt%) shown in Table 1 or 2, heated to 150°C, which is a temperature equal to or higher than the melting point of the amide, stirred using a magnetic stirrer, and then cooled to room temperature. The mixture was dispersed under pressure using a roller (triple roll) to prepare a grease composition.

    [0053] In Comparative Example 7, each component in the amount shown in Table 2 was dispersed directly without heating and cooling under pressure using a roller (triple roll) to prepare a grease composition.

    [Evaluation test]



    [0054] A friction test was performed at a load of 159 kg (350 lbf) for 15 minutes using a FALEX Pin and Vee Block tester to evaluate the amount of wear of the sample. In order to evaluate the performance when the grease has been used under severe conditions, the FALEX test was also performed using a flesh grease and a degraded grease that is obtained by leaving the flesh grease at 150°C for 100 hours or 500 hours.

    [Evaluation results]



    [0055] When only the mineral oil and the urea-based thickener were mixed, the amount of wear was about 7 mg when using the fresh grease, but was significantly large when using the degraded grease (Comparative Example 6).

    [0056] When the mineral oil, the urea-based thickener, and the solid lubricant were mixed, the amount of wear decreased to some extent when using the fresh grease, but was large when using the degraded grease (Comparative Examples 1 to 5).

    [0057] When the aliphatic amide was not heated and melted, the amount of wear was large when using the fresh grease and when using the degraded grease (Comparative Example 7).

    [0058] When the mineral oil, the urea-based thickener, the solid lubricant, and the aliphatic amide were mixed, the amount of wear significantly decreased when using the fresh grease and when using the degraded grease (Examples 1 to 9).
    [TABLE 1]
    Example   1 2 3 4 5 6 7 8 9 10
    Lubricant base oil Mineral oil 78 72 70 75 72 75   77 75 75
    P A O             75      
    Amide compound Stearic acid monoamide   13                
    Stearic acid bisamide 10     10 10 10 10 15 5  
    Oleic acid bisamide     15              
    Aromatic amide                   10
    Solid lubricant MCA 4 4 4 4     4 4 4 4
    P T F E         4          
    Boron nitride           4        
    Thickener Aliphatic diurea 7                  
    Alicyclic diurea   10 1 0 10 6 10 10 8 15 10
    Aromatic diurea         6          
    Antioxidant Diphenylamine 1 1 1 1 1 1 1 1 1 1
    Evaluation results Fresh grease: FALEX amount of wear 1.0 1.5 1. 3 1.2 1.0 0.9 1.0 0.9 1.8 1.5
    100h degraded grease: FALEX amount of wear 1.5 1.2 1.5 1.5 0.8 1.3 1.4 1.0 2.5 2.0
    500h degraded grease: FALEX amount of wear 1.8 1.2 2.0 1.5 1.3 1.0 1.3 1.0 2.2 2.1
    [TABLE 2]
    Comparative example 1 2 3 4 5 6 7
    Lubricant base oil Mineral oil 85 77 75 77 77 79 75
    Amide compound Stearic acid bisamide             10
    Solid lubricant MCA 4 4 4       4
    P T F E       4      
    Boron nitride         4    
    Thickener Aliphatic diurea 10            
    Alicyclic diurea   18 10 18 18 20 10
    Aromatic diurea     1 0        
    Antioxidant Diphenylamine 1 1 1 1 1 1 1
    Evaluation results Fresh grease: FALEX amount of wear 4.5 6.0 4.0 4.5 3.5 7.0 27
    100h degraded grease: FALEX amount of wear 25 28 30 27 32 28 -
    500h degraded grease: FALEX amount of wear 30 34 28 32 34 38 -
    In Comparative Example 7, the grease composition was prepared without heating and cooling after adding stearic acid bisamide.

    Industrial Applicability



    [0059] Since the grease composition according to the invention exhibits excellent water resistance, mechanical stability, and heat resistance, provides excellent wear resistance to metal-metal sliding parts at a low speed with a high load, and shows only a small extent of deterioration in wear resistance with long-term use under high temperatures, the grease composition can be used to lubricate a joint, a gear, and a bearing, and the like that have metal-metal sliding parts.


    Claims

    1. A grease composition comprising at least one base oil selected from a mineral oil-based lubricant base oil and a synthetic lubricant base oil, an amide compound, a solid lubricant, and a urea-based thickener, wherein the amide compound is heated and melted at least once together with the base oil,
    wherein the amide compound is a monoamide represented by the following general formula (1) and/or a bisamide represented by the following general formula (2) and/or a bisamide represented by the following general formula (3) and/or a triamide represented by the following general formula (4),

            R1-CO-NH-R2     (1)

            R1-CO-NH-A1-NH-CO-R2     (2)

            R1-NH-CO-A1-CO-NH-R2     (3)

            R1-M-A1-CH(A2-M-R3)-A3-M-R2     (4)

    wherein R1, R2, and R3 are independently a hydrocarbon group having 5 to 25 carbon atoms, R2 in the general formula (1) may be a hydrogen atom, A1, A2, and A3 are independently an aliphatic hydrocarbon group having 1 to 10 carbon atoms, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, or a divalent hydrocarbon group having 1 to 10 carbon atoms formed by combining these groups, some of the hydrogen atoms of the hydrocarbon group represented by R1, R2, or A1 in the general formulae (2) and (3) may be substituted with a hydroxyl group (-OH), and M is an amide group, wherein the solid lubricant is at least one selected from melamine cyanurate, polytetrafluoroethylene, and boron nitride,
    wherein the synthetic lubricant base oil is at least one selected from polyolefins, polyesters, polyalkylene glycols, alkylbenzenes and alkylnaphthalenes,
    the content of the amide compound in the grease composition is 0.1 to 50 mass%, based on the total amount of the grease composition,
    the content of the solid lubricant in the grease composition is 0.1 to 10 mass%, based on the total amount of the grease composition, and
    the content of the urea-based thickener in the grease composition is 2 to 30 mass%, based on the total amount of the grease composition.
     
    2. The grease composition according to claim 1, wherein the mineral oil-based lubricant base oil and the synthetic lubricant base oil have a kinematic viscosity of 1 to 1000 mm2/s at 40°C.
     
    3. The grease composition according to claim 1 or 2, wherein the amide compound includes an alkyl group having 6 to 24 carbon atoms.
     
    4. The grease composition according to any one of claims 1 to 3, wherein the urea-based thickener is at least one selected from an aliphatic diurea compound, an alicyclic diurea compound, and an aromatic diurea compound.
     
    5. Use of the grease composition according to any one of claims 1 to 4 for lubrication of metal-metal sliding parts.
     
    6. A method for producing the grease composition according to any one of claims 1 to 4, wherein the method comprises adding the amide compound to the base oil, followed by heating to melt the amide compound at least once.
     


    Ansprüche

    1. Schmiermittelzusammensetzung, umfassend mindestens ein Basisöl, ausgewählt aus einem Schmierstoff-Basisöl auf Mineralölbasis und einem synthetischen Schmierstoff-Basisöl, eine Amidverbindung, einen festen Schmierstoff und ein Verdickungsmittel auf Harnstoffbasis, wobei die Amidverbindung mindestens einmal zusammen mit dem Basisöl erwärmt und geschmolzen wird, wobei die Amidverbindung ein Monoamid, dargestellt durch die folgende allgemeine Formel (1) und/oder ein Bisamid, dargestellt durch die folgende allgemeine Formel (2), und/oder ein Bisamid, dargestellt durch die folgende allgemeine Formel (3) und/oder ein Triamid, dargestellt durch die folgende allgemeine Formel (4), ist

            R1-CO-NH-R2     (1)

            R1-CO-NH-A1-NH-CO-R2     (2)

            R1-NH-CO-A1-CO-NH-R2     (3)

            R1-M-A1-CH(A2-M-R3)-A3-M-R2     (4)

    wobei R1, R2 und R3 unabhängig eine Kohlenwasserstoffgruppe mit 5 bis 25 Kohlenstoffatomen sind, R2 in der allgemeinen Formel (1) ein Wasserstoffatom sein kann, A1, A2 und A3 unabhängig eine aliphatische Kohlenwasserstoffgruppe mit 1 bis 10 Kohlenstoffatomen, eine alicyclische Kohlenwasserstoffgruppe, eine aromatische Kohlenwasserstoffgruppe oder eine zweiwertige Kohlenwasserstoffgruppe mit 1 bis 10 Kohlenstoffatomen, gebildet durch Kombinieren dieser Gruppen, sind, einige der Wasserstoffatome der Kohlenwasserstoffgruppe, dargestellt durch R1, R2 oder A1 in den allgemeinen Formeln (2) und (3) mit einer Hydroxylgruppe (-OH) substituiert sein können und M eine Amidgruppe ist, wobei der feste Schmierstoff mindestens einer, ausgewählt aus Melamincyanurat, Polytetrafluorethylen und Bornitrid ist,
    wobei das synthetische Schmierstoff-Basisöl mindestens eines, ausgewählt aus Polyolefinen, Polyestern, Polyalkylenglykolen, Alkylbenzolen und Alkylnaphthalinen, ist
    der Gehalt der Amidverbindung in der Schmiermittelzusammensetzung 0,1 bis 50 Massen-%, bezogen auf die Gesamtmenge der Schmiermittelzusammensetzung, beträgt,
    der Gehalt des festen Schmierstoffs in der Schmiermittelzusammensetzung 0,1 bis 10 Massen-%, bezogen auf die Gesamtmenge der Schmiermittelzusammensetzung, beträgt und
    der Gehalt des Verdickungsmittels auf Harnstoffbasis in der Schmiermittelzusammensetzung 2 bis 30 Massen-%, bezogen auf die Gesamtmenge der Schmiermittelzusammensetzung, beträgt.
     
    2. Schmiermittelzusammensetzung nach Anspruch 1, wobei das Schmierstoff-Basisöl auf Mineralölbasis und das synthetische Schmierstoff-Basisöl eine kinematische Viskosität von 1 bis 1000 mm2/s bei 40°C aufweisen.
     
    3. Schmiermittelzusammensetzung nach Anspruch 1 oder 2, wobei die Amidverbindung eine Alkylgruppe mit 6 bis 24 Kohlenstoffatomen einschließt.
     
    4. Schmiermittelzusammensetzung nach einem der Ansprüche 1 bis 3, wobei das Verdickungsmittel auf Harnstoffbasis mindestens eines, ausgewählt aus einer aliphatischen Diharnstoffverbindung, einer alicyclischen Diharnstoffverbindung und einer aromatischen Diharnstoffverbindung, ist.
     
    5. Verwendung der Schmiermittelzusammensetzung nach einem der Ansprüche 1 bis 4 zum Schmieren von Metall-Metall-Gleitteilen.
     
    6. Verfahren zur Herstellung der Schmiermittelzusammensetzung nach einem der Ansprüche 1 bis 4, wobei das Verfahren das Zugeben der Amidverbindung zu dem Basisöl, gefolgt von Erwärmen, um die Amidverbindung mindestens ein Mal zu schmelzen, umfasst.
     


    Revendications

    1. Composition de graisse comprenant au moins une huile de base sélectionnée parmi une huile de base lubrifiante à base d'huile minérale et une huile de base lubrifiante synthétique, un composé d'amide, un lubrifiant solide et un épaississant à base d'urée, dans laquelle le composé d'amide est chauffé et tondu au moins une fois avec l'huile de base,
    dans laquelle le composé d'amide est un monoamide représenté par la formule générale suivante (1) et/ou un bisamide représenté par la formule générale suivante (2) et/ou un bisamide représente par la formule générale suivante (3) et/ou un triamide représenté par la formule générale suivante (4),

            R1-CO-NH-R2     (1)

            R1-CO-NH-A1-NH-CO-R2     (2)

            R1-NH-CO-A1-CO-NH-R2     (3)

            R1-M-A1-CH(A2-M-R3)-A3-M-R2     (4)

    dans lesquelles R1, R2 et R3 sont indépendamment un groupe hydrocarbure ayant 5 à 25 atomes de carbone, R2 dans la formule générale (1) peut être un atome d'hydrogène, A1, A2 et A3 sont indépendamment un groupe hydrocarbure aliphatique ayant 1 à 10 atomes de carbone, un groupe hydrocarbure alicyclique, un groupe hydrocarbure aromatique ou un groupe hydrocarbure divalent ayant 1 à 10 atomes de carbone formé en combinant ces groupes, certains des atomes d'hydrogène du groupe hydrocarbure représenté par R1, R2 ou A1 dans les formules générales (2) et (3) peuvent être substitués par un groupe hydroxyle (-OH) et M est un groupe amide,
    dans laquelle le lubrifiant solide est au moins un sélectionné parmi le cyanurate de mélamine, polytétrafluoroéthylène et nitrure de bore,
    dans laquelle l'huile de base lubrifiante synthétique est au moins une sélectionnée parmi des polyoléfines, polyesters, polyalkylèneglycols, alkylbenzènes et alkylnaphtalènes,
    la teneur en le composé d'amide dans la composition de graisse est de 0,1 à 50 % en masse, basée sur la quantité totale de la composition de graisse,
    la teneur en le lubrifiant solide dans la composition de graisse est de 0,1 à 10 % en masse, basée sur la quantité totale de la composition de graisse, et
    la teneur en l'épaississant à base d'urée dans la composition de graisse est de 2 à 30 % en masse, basée sur la quantité totale de la composition de graisse.
     
    2. Composition de graisse selon la revendication 1, dans laquelle l'huile de base lubrifiante à base d'huile minérale et l'huile de base lubrifiante synthétique ont une viscosité cinématique de 1 à 1000 mm2/s à 40°C.
     
    3. Composition de graisse selon la revendication 1 ou 2, dans laquelle le composé d'amide inclut un groupe alkyle ayant 6 à 24 atomes de carbone.
     
    4. Composition de graisse selon l'une quelconque des revendications 1 à 3, dans laquelle l'épaississant à base d'urée est au moins un sélectionné parmi un composé de diurée aliphatique, un composé de diurée alicyclique et un composé de diurée aromatique.
     
    5. Utilisation de la composition de graisse selon l'une quelconque des revendications 1 à 4 pour la lubrification de parties coulissantes métal-métal.
     
    6. Procédé de production de la composition de graisse selon l'une quelconque des revendications 1 à 4, dans lequel le procédé comprend ajouter le composé d'amide à l'huile de base, suivi du chauffage pour faire fondre le composé d'amide au moins une fois.
     






    Cited references

    REFERENCES CITED IN THE DESCRIPTION



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    Patent documents cited in the description