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US20130116158A1 - Lubricant compositions and rolling device - Google Patents

Lubricant compositions and rolling device Download PDF

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Publication number
US20130116158A1
US20130116158A1 US13/580,485 US201213580485A US2013116158A1 US 20130116158 A1 US20130116158 A1 US 20130116158A1 US 201213580485 A US201213580485 A US 201213580485A US 2013116158 A1 US2013116158 A1 US 2013116158A1
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US
United States
Prior art keywords
lubricant
raceway surface
fatty acid
inner member
test
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
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US13/580,485
Inventor
Koichi Hachiya
Kanako Mori
Atsushi Yokouchi
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NSK Ltd
Original Assignee
NSK Ltd
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Priority claimed from JP2011133118A external-priority patent/JP2012126880A/en
Application filed by NSK Ltd filed Critical NSK Ltd
Assigned to NSK LTD. reassignment NSK LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HACHIYA, KOICHI, MORI, KANAKO, YOKOUCHI, ATSUSHI
Publication of US20130116158A1 publication Critical patent/US20130116158A1/en
Abandoned legal-status Critical Current

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    • 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
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/26Carboxylic acids; Salts thereof
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, 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
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/06Mixtures of thickeners and additives
    • 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
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C33/00Parts of bearings; Special methods for making bearings or parts thereof
    • F16C33/30Parts of ball or roller bearings
    • F16C33/66Special parts or details in view of lubrication
    • F16C33/6603Special parts or details in view of lubrication with grease as lubricant
    • F16C33/6607Retaining the grease in or near the bearing
    • 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
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C33/00Parts of bearings; Special methods for making bearings or parts thereof
    • F16C33/30Parts of ball or roller bearings
    • F16C33/66Special parts or details in view of lubrication
    • F16C33/6603Special parts or details in view of lubrication with grease as lubricant
    • F16C33/6633Grease properties or compositions, e.g. rheological properties
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
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    • C10M2203/022Well-defined aliphatic compounds saturated
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/024Well-defined aliphatic compounds unsaturated
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/026Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/046Hydroxy ethers
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    • C10M2207/08Aldehydes; Ketones
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/1256Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids used as thickening agent
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/126Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/126Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
    • C10M2207/1265Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic used as thickening agent
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/128Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids containing hydroxy groups; Ethers thereof
    • C10M2207/1285Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids containing hydroxy groups; Ethers thereof used as thickening agents
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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    • C10M2207/283Esters of polyhydroxy compounds
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
    • C10M2207/2835Esters of polyhydroxy compounds used as base material
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • C10M2207/401Fatty vegetable or animal oils used as base material
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
    • C10M2215/065Phenyl-Naphthyl amines
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/10Amides of carbonic or haloformic acids
    • C10M2215/102Ureas; Semicarbazides; Allophanates
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/10Amides of carbonic or haloformic acids
    • C10M2215/102Ureas; Semicarbazides; Allophanates
    • C10M2215/1026Ureas; Semicarbazides; Allophanates used as thickening material
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/06Thio-acids; Thiocyanates; Derivatives thereof
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    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
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    • 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
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    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/64Environmental friendly compositions
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings
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    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
    • 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
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C19/00Bearings with rolling contact, for exclusively rotary movement
    • F16C19/02Bearings with rolling contact, for exclusively rotary movement with bearing balls essentially of the same size in one or more circular rows
    • F16C19/04Bearings with rolling contact, for exclusively rotary movement with bearing balls essentially of the same size in one or more circular rows for radial load mainly
    • F16C19/06Bearings with rolling contact, for exclusively rotary movement with bearing balls essentially of the same size in one or more circular rows for radial load mainly with a single row or balls

Definitions

  • the present invention relates to lubricant compositions.
  • the invention further relates to a rolling device, e.g., a rolling bearing, ball screw, linear guide, or direct-acting bearing.
  • Lubricant compositions such as lubricating oils and greases have conventionally been used in the sliding parts or rotating or rolling parts of various machines and apparatus (see, for example, patent documents 1 to 3).
  • most of the conventionally known lubricant compositions including those of patent documents 1 to 3 are not eatable, and there are few known lubricant compositions, among the lubricant compositions usable for lubricating machine parts including rolling bearings, that are harmless even when eaten.
  • oxidation inhibitors are added to lubricant compositions to improve the durability thereof, because the temperature of the lubricant compositions rises with operation of the rolling devices.
  • the oxidation inhibitors for addition to lubricant compositions include the following. Frequently used for industrial applications are amine-based antioxidants, phenolic antioxidants, and phenothiazine. There are cases where tocopherol (vitamin E), dibutyl-p-cresol (DBPC), butylhydroxyanisole (BHA), butylhydroquinone (TBHQ), isopropyl gallate, and the like are used in machines for foods, although such cases are rare (see, for example, patent documents 4 to 6). However, there is considerable concern about environmental preservation, and there is a strong desire for a technique which imposes little environmental burden and, despite this, further enhances the effect of oxidation prevention.
  • An object of the invention which has been achieved in view of the circumstances described above, is to provide lubricant compositions which are harmless even when eaten, have excellent lubricity, and impose little environmental burden and which, despite this, are highly prevented from oxidizing. Another object is to provide a rolling device which is lubricant with either of the lubricant compositions, imposes little environmental burden, and is excellent in terms of lubrication and durability.
  • the present invention provides the following lubricant compositions and rolling device in order to overcome those problems.
  • the lubricant compositions of the invention are harmless even when eaten, and impose little environmental burden. Despite this, the compositions are highly prevented from oxidizing.
  • the rolling device of the invention has excellent durability, imposes little environmental burden, and causes no harm even when the lubricant composition is eaten.
  • FIG. 1 is a sectional view which illustrates a deep-groove ball bearing as one embodiment of the rolling device of the invention.
  • FIG. 2 is a graph which shows the results of (Test 1) conducted in Example A.
  • FIG. 3 is a graph that shows the results of an examination in which the test greases of Examples 4A, 5A, and 6A and Comparative Examples 20A and 21A were examined for bearing life in (Test 2) in Example A.
  • FIG. 4 is a graph that shows the results of an examination in which the test greases of Examples 7A and 8A and Comparative Examples 22A and 23A were examined for bearing life in (Test 2) in Example A.
  • FIG. 5 is a graph which shows the results of a life test conducted in Example B.
  • FIG. 6 is a graph which shows the results of another life test conducted in Example B.
  • FIG. 7 is a graph which shows the results of still another life test conducted in Example B.
  • FIG. 8 is a graph which shows the results of Example C.
  • FIG. 9 is a graph which shows the results of Example D.
  • One of the lubricant compositions of the invention includes a saturated fatty acid triglyceride as a lubricating ingredient and an antioxidant as an oxidation inhibitor.
  • the saturated fatty acid triglyceride is an ester of one or more saturated fatty acids with glycerol, and has biodegradability.
  • the kinds of the saturated fatty acids are not particularly limited. However, linear fatty acids are preferred, and saturated fatty acids having 6-12 carbon atoms are preferred. In case where the saturated fatty acids each have 5 or less carbon atoms, there is the possibility that the base oil might have insufficient heat resistance. In case where the saturated fatty acids each have more than 12 carbon atoms, there is the possibility that the base oil might have too high a viscosity. Preferred of those are saturated fatty acids having 8-12 carbon atoms. Even more preferred are saturated fatty acids having 8-10 carbon atoms. Such saturated fatty acids have excellent lubricity and are available on the market at relatively low cost.
  • One saturated fatty acid triglyceride may be used alone, or a plurality of saturated fatty acid triglycerides may be used as a mixture thereof. Furthermore, the saturated fatty acid triglyceride may be either a saturated fatty acid triglyceride obtained by the reaction of three molecules of one saturated fatty acid with one molecule of glycerol or a saturated fatty acid triglyceride obtained by the reaction of three molecules, in total, of two or three saturated fatty acids with one molecule of glycerol.
  • the mixture should be a mixture of a saturated fatty acid triglyceride which is an ester of a saturated fatty acid having 8 carbon atoms with glycerol (referred to as saturated fatty acid triglyceride A) and a saturated fatty acid triglyceride which is an ester of a saturated fatty acid having 10 carbon atoms with glycerol (referred to as saturated fatty acid triglyceride B).
  • the molar ratio of the saturated fatty acid triglyceride A to the saturated fatty acid triglyceride B is preferably in the range of 60:40 to 90:10, more preferably in the range of 70:30 to 80:20.
  • the lubricant composition has better chemical performance, e.g., heat resistance and durability, and better mechanical performance, not to mention better low-torque characteristics.
  • this triglyceride should be a saturated fatty acid triglyceride obtained by the reaction of three molecules, in total, of a saturated fatty acid having 8 carbon atoms and a saturated fatty acid having 10 carbon atoms with one molecule of glycerol.
  • the molar ratio of the saturated fatty acid ingredient having 8 carbon atoms (C) to the saturated fatty acid ingredient having 10 carbon atoms (D) (C:D) is preferably in the range of 60:40 to 90:10, more preferably in the range of 70:30 to 80:20.
  • the lubricant composition has better chemical performance, e.g., heat resistance and durability, and better mechanical performance, not to mention better low-torque characteristics.
  • the molar ratio (C:D) can be regulated, for example, by mixing, in a suitable proportion, a saturated fatty acid triglyceride obtained by the reaction of one molecule of the saturated fatty acid having 8 carbon atoms and two molecules of the saturated fatty acid having 10 carbon atoms with one molecule of glycerol and a saturated fatty acid triglyceride obtained by the reaction of two molecules of the saturated fatty acid having 8 carbon atoms and one molecule of the saturated fatty acid having 10 carbon atoms with one molecule of glycerol.
  • the saturated fatty acid triglyceride should have a dynamic viscosity at 40° C. of 8-120 mm 2 /s.
  • the dynamic viscosity at 40° C. thereof is less than 8 mm 2 /s, there is the possibility that the base oil might have insufficient heat resistance.
  • this base oil has increased shear resistance and there is the possibility that use of this lubricant composition in, for example, a rolling bearing might disadvantageously result in an increase in starting torque or rotation torque.
  • the dynamic viscosity at 40° C. of the saturated fatty acid triglyceride is more preferably 8-50 mm 2 /s, even more preferably 10-35 mm 2 /s, most preferably 10-20 mm 2 /s.
  • the lubricant composition should consist only of one or more saturated fatty acid triglycerides or contain one or more saturated fatty acid triglycerides as the main component.
  • another kind of oil which is used as a base oil in general lubricants may be mixed with the saturated fatty acid triglyceride(s) so long as the oil is incorporated in such an amount that the objects of the invention are accomplished.
  • a natural lubricating oil such as an animal or vegetable oil is preferred. Examples thereof include beef tallow, lard, soybean oil, rapeseed oil, rice bran oil, coconut oil, palm oil, and palm kernel oil or products of hydrogenation of these.
  • the antioxidant may be an antioxidant which is in use as a food additive.
  • the lubricant composition or the rolling device, e.g., a rolling bearing, that is equipped with the lubricant composition is rendered usable in machines for foods, machines for medicines, etc.
  • antioxidant include phenols, polyphenols, flavonoids, carotenoids, vitamins, vitamin analogues, and organic acids.
  • phenols examples include BHA, butylhydroxytoluene (BHT), and TBHQ.
  • polyphenols examples include grape seed extract, proanthocyanidin, and oil-soluble catechins.
  • flavonoids examples include soybean isoflavone.
  • Examples of the cateroids include ⁇ -carotene, lycopene, and astaxanthin.
  • vitamins examples include vitamin A substances, vitamin B substances, vitamin C substances, vitamin D substances, vitamin E substances, and vitamin K substances.
  • vitamin A substances include retinal, retinol, retinoic acid, and dehydroretinal.
  • vitamin B substances include thiamine, thiamine disulfide, dicethiamine, octotiamine, cycotiamine, bisibuthiamine, bisbentiamine, prosultiamine, benfotiamine, fursultiamine, riboflavin, flavin adenine dinucleotide, pyridoxine, pyridoxal, hydroxocobalamin, cyanocobalamin, methylcobalamin, deoxyadenocobalamin, folic acid, tetrahydrofolic acid, dihydrofolic acid, nicotinic acid, nicotinamide, nicotinyl alcohol, pantothenic acid, panthenol, biotin, cho
  • Examples of the vitamin C substances include ascorbic acid and derivatives thereof and erythorbic acid and derivatives thereof.
  • Examples of the vitamin D substances include ergocalciferol, cholecalciferol, hydroxycholecalciferol, dihydroxycholecalciferol, and dihydrotachysterol.
  • Examples of the vitamin E substances include tocopherols, derivatives thereof, and ubiquinone derivatives.
  • the tocopherols are not particularly limited, and examples thereof include d- ⁇ -tocopherol, d- ⁇ -tocopherol, d- ⁇ -tocopherol, d- ⁇ -tocopherol, and dl- ⁇ -tocopherol. A mixture of these tocopherols may be used.
  • vitamin K substances examples include phytonadione, menaquinone, menadione, menadiol, an extract of fermented soybeans, and an extract of Bacillus natto.
  • examples of other vitamin substances include carnitine, ferulic acid, ⁇ -orizanol, orotic acid, rutin, eriocitrin, and hesperidin.
  • vitamin analogues examples include thioctic acid ( ⁇ -liboic acid) and ubiquinol.
  • organic acids examples include phytic acid.
  • One of these antioxidants may be used alone, or a suitable combination of two or more thereof may be used. To use two or more thereof in combination further enhances the effect of preventing oxidation.
  • the content of the antioxidant in the lubricant composition is an amount with which the effect of preventing oxidation can be imparted.
  • the content thereof can be regulated in accordance with the kind of the lubricating ingredient, use, etc.
  • a sufficient oxidation-preventing effect is obtained by incorporating the antioxidant in an amount of 0.1-10% by mass based on the whole grease.
  • coenzyme Q it is preferred to add a coenzyme Q to the lubricant composition, because the addition thereof further enhances the oxidation-preventing effect.
  • the kind of the coenzyme Q is not particularly limited, coenzyme Q10 is especially preferred.
  • One coenzyme Q may be used alone, or a suitable combination of two or more coenzymes Q may be used.
  • a thickener may be incorporated to produce a grease composition.
  • the thickener include metal soaps such as aluminum soaps, barium soaps, calcium soaps, lithium soaps, sodium soaps, lithium complex soaps, calcium complex soaps, and aluminum complex soaps.
  • metal soaps such as aluminum soaps, barium soaps, calcium soaps, lithium soaps, sodium soaps, lithium complex soaps, calcium complex soaps, and aluminum complex soaps.
  • urea compounds such as diurea, triurea, tetraurea, and polyurea, urethane compounds, urea-urethane compounds, sodium terephthalamate, and the like.
  • gellants such as amino acid-based gellants and polysaccharide esters, are also usable.
  • a dextrin fatty acid ester which is obtained from a fatty acid and dextrin
  • an inulin fatty acid ester which is obtained from a fatty acid and inulin
  • these esters are materials derived from natural substances, the burden to be imposed on the environment is lessened.
  • various bacteria are apt to propagate and the grease composition is apt to be deteriorated by the propagation of bacteria. This bacterial deterioration of the grease composition can be inhibited by using, as an antioxidant, thioctic acid in combination with at least one member selected from vitamin E substances and polyphenols.
  • the fatty acids of the dextrin fatty acid ester and inulin fatty acid ester should be saturated fatty acids having 6-24 carbon atoms.
  • saturated fatty acids having 6-24 carbon atoms.
  • examples thereof include hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, dodecanoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid, heptadecanoic acid, octadecanoic acid, nanodecanoic acid, icosanoic acid, docosanoic acid, and tetradocosanoic acid.
  • Preferred of these are pentadecanoic acid, hexadecanoic acid, and heptadecanoic acid. It is preferred that these saturated fatty acids should have a linear structure.
  • dextrin is a saccharide formed by polymerizing a plurality of ⁇ -glucose molecules through glycoside bonds, and is generally obtained by hydrolyzing a starch.
  • Inulin also is a polysaccharide, and is designated as CAS No. 9005-8-5. Consequently, these substances exert no influence on the environment.
  • the amount of the thickener is not limited so long as the saturated fatty acid triglyceride can be thickened thereby, and the amount thereof can be suitably set in accordance with the desired worked consistency, torque, etc. However, the amount thereof is preferably 10-40% by mass based on the whole grease.
  • a saturated fatty acid triglyceride as a base oil and either magnesium stearate or calcium stearate as a thickener. It is preferred that the magnesium stearate and the calcium stearate to be used each should be of a food additive or medicine additive grade which meets standards such as the Japanese Standards for Food Additives or the Japanese Pharmacopoeia.
  • the content of the magnesium stearate or calcium stearate in the grease composition is not particularly limited. However, the content thereof is preferably 12-35% by mass. So long as the content thereof is within that range, the grease composition, when applied to a rolling device, can be inhibited from leaking out from the sliding part or rolling part. As a result, the rolling device can be lubricated over a long period. In case where the content thereof is less than 12% by mass, this grease composition has reduced shear stability and, hence, there is the possibility that this grease composition, when applied to a rolling device, might be softened by shearing in the sliding part or rolling part to accelerate the leakage of the grease composition from the sliding part or rolling part.
  • the rolling device cannot be lubricated over a long period.
  • the content of the thickener exceeds 35% by mass, the proportion of the base oil in the grease composition is low and, hence, there is the possibility that this grease composition might have insufficient lubricity.
  • the content of the thickener in the grease composition is more preferably 12-28% by mass, even more preferably 12-25% by mass, most preferably 15-25% by mass.
  • Additives which are in general use in lubricants may be further added to the lubricant composition in order to further improve the various performances of the lubricant composition.
  • examples thereof include rust preventives, extreme-pressure agents, friction regulators, pH regulators, antiwear agents, oiliness improvers, and metal deactivators.
  • additives which contain a metallic element are undesirable from the standpoint of the environment.
  • One of those additives may be used alone, or a suitable combination of two or more thereof may be used.
  • the total content of the additives in the lubricant composition is not particularly limited unless the additives defeat the objects of the invention.
  • the rolling device of the invention is lubricated with the lubricant composition or grease composition described above.
  • the rolling device includes deep-groove ball bearings such as that shown in FIG. 1 .
  • the deep-groove ball bearing shown in the figure is equipped with: an inner ring 1 which has a raceway surface 1 a in the outer circumferential surface thereof; an outer ring 2 which has, in the inner circumferential surface thereof, a raceway surface 2 a that faces the raceway surface la and which has been disposed radially outside the inner ring 1 ; a plurality of rolling elements (balls) 3 which have been disposed between the two raceway surfaces 1 a and 2 a so as to be freely rollable; a cage 4 which holds the multiple rolling elements 3 between the inner ring 1 and the outer ring 2 ; and sealing devices 5 and 5 which serve as seals that close the space openings present between the inner ring 1 and the outer ring 2 .
  • the cage 4 and the sealing devices 5 may be
  • the grease composition described above is filled into the space (bearing space) which has been formed between the inner ring 1 and the outer ring 2 and in which the rolling elements 3 have been disposed, in order to lubricate between each raceway surface 1 a or 2 a and the rolling elements 3 . Consequently, the rolling device of the invention has excellent durability and exerts little influence on the environment.
  • the embodiment shown is a mere example of the invention, and the invention should not be construed as being limited to the embodiment.
  • the invention can be applied to other rolling bearings of various kinds
  • the invention is applicable to radial rolling bearings such as angular ball bearings, self-aligning ball bearings, cylindrical roller bearings, tapered roller bearings, needle roller bearings, and self-aligning roller bearings and thrust rolling bearings such as thrust ball bearings and thrust roller bearings.
  • Applications of the invention are not limited to such rolling bearings, and the invention is further applicable to other rolling devices of various kinds, such as, for example, ball screws, direct-acting guides, and direct-acting bearings.
  • Thioctic acid ( ⁇ -LI), d- ⁇ -tocopherol (V.E.), catechin (Kat), dibutylhydroxytoluene (BHT), isoflavone (IF), ⁇ -carotene (Car), and butylhydroxyanisole (BHA) were added alone or in combination as shown in Table 1 to a saturated medium-chain fatty acid triglyceride (“Panasate 875”, manufactured by NOF Corp.) to prepare test lubricating oils.
  • the addition amounts of those antioxidants were as follows. When an antioxidant compound was used alone, the compound was added in an amount of 2.5% by mass. When a mixture of two antioxidant compounds was used, each compound was added in an amount of 1.25% by mass, the total amount thereof being 2.5% by mass.
  • Example 1A Example 2A
  • Example 3A ⁇ -LI ⁇ -LI ⁇ -LI V.E.
  • Kat Comparative Comparative Comparative Comparative Comparative Comparative Example 1A Example 2A
  • Example 3A Example 4A BHT V.E. IF Kat BHT BHT BHT Comparative Comparative Comparative Comparative Comparative Example 5A
  • Example 6A Example 7A
  • Example 8A Car BHA V.E. IF BHT BHT V.E. Comparative Comparative Comparative Comparative Comparative Example 9A
  • Example 10A Example 11A
  • Example 12A Car BHA IF Car V.E. V.E.
  • test lubricating oils of Examples 1A to 3A contained thioctic acid alone or contained a mixture of thioctic acid with catechin or d- ⁇ -tocopherol. It can be seen that these lubricating oils were inhibited from suffering an increase in viscosity due to heating.
  • the thickener use was made of dextrin hexadecanoate, lithium 12-hydroxystearate, or a product of reaction between stearylamine and 4,4′-diphenylmethane diisocyanate (C18-MDI urea).
  • the amounts of the thickeners in the base greases were 15% by mass for dextrin hexadecanoate, 12% by mass for lithium 12-hydroxystearate, and 15% by mass for the urea.
  • the base greases had been regulated so as to have the shown consistency values.
  • Test greases were prepared in accordance with the formations shown in
  • the grease of Example 1B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa ⁇ s as a base oil and an aluminum complex soap as a thickener, and which had been obtained by adding an antioxidant and coenzyme Q10 to the base oil and thickener in an amount of 2.5% by mass each.
  • MCT medium-chain fatty acid triglyceride
  • the kind of the antioxidant added was dl- ⁇ -tocopherol as shown in Table 4.
  • the grease of Example 2B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa ⁇ s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant and coenzyme Q10 to the base oil and thickener in an amount of 2.5% by mass each.
  • MCT medium-chain fatty acid triglyceride
  • the kind of the antioxidant added was d- ⁇ -tocopherol as shown in Table 4.
  • the grease of Example 3B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa ⁇ s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant and coenzyme Q10 to the base oil and thickener in an amount of 2.5% by mass each.
  • MCT medium-chain fatty acid triglyceride
  • the kind of the antioxidant added was a natural type vitamin E which was on the market as a mixture of d- ⁇ -tocopherol and d- ⁇ -tocopherol, as shown in Table 4.
  • the grease of Example 4B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa ⁇ s as a base oil and a urea compound as a thickener, and which had been obtained by adding an antioxidant and coenzyme Q10 to the base oil and thickener in an amount of 2.5% by mass each.
  • MCT medium-chain fatty acid triglyceride
  • a urea compound as a thickener, and which had been obtained by adding an antioxidant and coenzyme Q10 to the base oil and thickener in an amount of 2.5% by mass each.
  • the kind of the antioxidant added was d- ⁇ -tocopherol as shown in Table 4.
  • the urea compound was a compound synthesized by reacting 1 mol of diphenylmethane 4,4′-diisocyanate (MDI) with 2 mol of stearylamine.
  • MDI diphenyl
  • the grease of Comparative Example 1B was a grease which included a polyol ester oil having a dynamic viscosity at 40° C. of 32.6 mPa ⁇ s as a base oil and lithium 12-hydroxystearate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass.
  • the kind of the antioxidant added was dl- ⁇ -tocopherol as shown in Table 4.
  • the grease of Comparative Example 2B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa ⁇ s as a base oil and an aluminum complex soap as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass.
  • MCT medium-chain fatty acid triglyceride
  • the kind of the antioxidant added was dl- ⁇ -tocopherol as shown in Table 4.
  • the grease of Comparative Example 3B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa ⁇ s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass.
  • MCT medium-chain fatty acid triglyceride
  • the kind of the antioxidant added was d- ⁇ -tocopherol as shown in Table 4.
  • the grease of Comparative Example 4B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa ⁇ s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass.
  • MCT medium-chain fatty acid triglyceride
  • the kind of the antioxidant added was a natural type vitamin E which was on the market as a mixture of d- ⁇ -tocopherol and d- ⁇ -tocopherol, as shown in Table 4.
  • the grease of Comparative Example 5B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa ⁇ s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass.
  • MCT medium-chain fatty acid triglyceride
  • the kind of the antioxidant added was d- ⁇ -tocopherol as shown in Table 4.
  • the urea compound was a compound synthesized by reacting 1 mol of diphenylmethane 4,4′-diisocyanate (MDI) with 2 mol of stearylamine.
  • the grease of Comparative Example 6B was a grease which included rapeseed oil having a dynamic viscosity at 40° C. of 32 mPa ⁇ s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass.
  • the kind of the antioxidant added was d- ⁇ -tocopherol as shown in Table 4.
  • the grease of Comparative Example 7B was a grease which included rapeseed oil having a dynamic viscosity at 40° C. of 32 mPa ⁇ s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass.
  • the kind of the antioxidant added was a natural type vitamin E which was on the market as a mixture of d- ⁇ -tocopherol and d- ⁇ -tocopherol, as shown in Table 4.
  • Comparative Examples 1B to 7B were 12% by mass.
  • the values of worked consistency and unworked consistency of these test greases were as shown in Table 4.
  • Comparative Examples 2B, 3B, 4B, and 5B are Reference Examples for ascertaining the effect of the coenzyme Q.
  • Example 1B and Comparative Examples 1B and 2B With respect to the test greases of Example 1B and Comparative Examples 1B and 2B, 3.4 g of each test grease was enclosed in rolling bearing No. 6305VVC3E, and this rolling bearing was rotated under the conditions of an ambient temperature of 120° C., an axial load of 98 N, and a rotation speed of 10,000 min ⁇ 1 . The period required for the driving motor for rotating the rolling bearing to stop due to overload was measured, and this period was taken as the life.
  • test greases thus produced were filled, in an amount of 1.0 g, into the bearing space of deep-groove ball bearing No. 6203VV (inner diameter, 17 mm; outer diameter, 40 mm).
  • inner diameter, 17 mm; outer diameter, 40 mm the bearing space of deep-groove ball bearing No. 6203VV (inner diameter, 17 mm; outer diameter, 40 mm).
  • three test bearings were obtained.
  • These test bearings were subjected to a rotation test at various rotation speeds (1,800-7,500 min ⁇ 1 ) and examined for rotation torque.
  • the axial load was set at 196 N, and the test temperature was room temperature.
  • the rotation torque was measured throughout the period from the time when 550 seconds had passed since the initiation of rotation to the time when 600 seconds had passed since the rotation initiation, and the average value thereof was taken as the rotation torque of this test bearing.
  • the results thereof are shown as a graph in FIG. 8 .
  • the abscissa of the graph in FIG. 8 is the value of dmN determined from the rotation speed during the test.
  • the test bearing equipped with the test grease of Example 1C showed excellent low-torque characteristics at each rotation speed as compared with the test bearings equipped with the test greases of Comparative Examples 1C and 2C.
  • a rotation torque test was conducted in the same manner as in Example C. The results thereof are shown as a graph in FIG. 9 .
  • the abscissa of the graph in FIG. 9 is the value of dmN determined from the rotation speed during the test.
  • the test bearing equipped with the test grease of Example 1D showed excellent low-torque characteristics at each rotation speed as compared with the test bearings equipped with the test greases of Comparative Examples 1D and 2D.
  • the lubricant compositions and rolling device of the invention are useful in or as the rotating parts or sliding parts of various machines and apparatus.
  • the lubricant compositions are harmless even when eaten, and impose little burden on the environment. Consequently, the lubricant compositions and the rolling device are useful especially in machines and apparatus which relate to foods or medical supplies.

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Abstract

The lubricant compositions of the invention include a saturated fatty acid triglyceride as a lubricating ingredient and further contain an antioxidant or a thickener which is magnesium stearate or calcium stearate. Consequently, the lubricant compositions are harmless even when eaten, have excellent lubricity, and impose little burden on the environment. The rolling device of the invention not only imposes little burden on the environment because the device is lubricated with either of these lubricant compositions, but also has excellent durability.

Description

    TECHNICAL FIELD
  • The present invention relates to lubricant compositions. The invention further relates to a rolling device, e.g., a rolling bearing, ball screw, linear guide, or direct-acting bearing.
  • BACKGROUND ART
  • Lubricant compositions such as lubricating oils and greases have conventionally been used in the sliding parts or rotating or rolling parts of various machines and apparatus (see, for example, patent documents 1 to 3). However, most of the conventionally known lubricant compositions including those of patent documents 1 to 3 are not eatable, and there are few known lubricant compositions, among the lubricant compositions usable for lubricating machine parts including rolling bearings, that are harmless even when eaten.
  • There are frequently cases where oxidation inhibitors are added to lubricant compositions to improve the durability thereof, because the temperature of the lubricant compositions rises with operation of the rolling devices. The oxidation inhibitors for addition to lubricant compositions include the following. Frequently used for industrial applications are amine-based antioxidants, phenolic antioxidants, and phenothiazine. There are cases where tocopherol (vitamin E), dibutyl-p-cresol (DBPC), butylhydroxyanisole (BHA), butylhydroquinone (TBHQ), isopropyl gallate, and the like are used in machines for foods, although such cases are rare (see, for example, patent documents 4 to 6). However, there is considerable concern about environmental preservation, and there is a strong desire for a technique which imposes little environmental burden and, despite this, further enhances the effect of oxidation prevention.
  • PRIOR-ART DOCUMENTS Patent Documents
    • Patent Document 1: Japanese Patent No. 4730714
    • Patent Document 2: JP-T-2004-510020
    • Patent Document 3: JP-A-2007-64456
    • Patent Document 4: JP-A-2002-323053
    • Patent Document 5: JP-A-2008-248990
    • Patent Document 6: JP-A-4-72392
    SUMMARY OF THE INVENTION Problems that the Invention is to Solve
  • An object of the invention, which has been achieved in view of the circumstances described above, is to provide lubricant compositions which are harmless even when eaten, have excellent lubricity, and impose little environmental burden and which, despite this, are highly prevented from oxidizing. Another object is to provide a rolling device which is lubricant with either of the lubricant compositions, imposes little environmental burden, and is excellent in terms of lubrication and durability.
  • Means for Solving the Problems
  • The present invention provides the following lubricant compositions and rolling device in order to overcome those problems.
    • (1) A lubricant composition characterized by comprising a saturated fatty acid triglyceride and an antioxidant.
    • (2) The lubricant composition according to (1) above characterized in that the antioxidant comprises at least one member selected from phenols, polyphenols, flavonoids, carotenoids, vitamins, vitamin analogues, and organic acids.
    • (3) The lubricant composition according to (1) or (2) above characterized by containing a coenzyme Q.
    • (4) The lubricant composition according to any one of (1) to (3) above characterized by containing a fatty acid ester, a metal soap, or a urea compound as a thickener.
    • (5) A lubricant composition characterized by comprising a saturated fatty acid triglyceride as a base oil and either magnesium stearate or calcium stearate as a thickener.
    • (6) A rolling device equipped with an inner member which has a raceway surface in the outer surface thereof, an outer member which has a raceway surface that faces the raceway surface of the inner member and which has been disposed outside the inner member, a plurality of rolling elements which have been disposed between the two raceway surfaces so as to be freely rollable, and a lubricant which lubricates between each raceway surface and the rolling elements, characterized in that the lubricant is the lubricant composition according to any one of (1) to (5) above.
    Effects of the Invention
  • The lubricant compositions of the invention are harmless even when eaten, and impose little environmental burden. Despite this, the compositions are highly prevented from oxidizing. The rolling device of the invention has excellent durability, imposes little environmental burden, and causes no harm even when the lubricant composition is eaten.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a sectional view which illustrates a deep-groove ball bearing as one embodiment of the rolling device of the invention.
  • FIG. 2 is a graph which shows the results of (Test 1) conducted in Example A.
  • FIG. 3 is a graph that shows the results of an examination in which the test greases of Examples 4A, 5A, and 6A and Comparative Examples 20A and 21A were examined for bearing life in (Test 2) in Example A.
  • FIG. 4 is a graph that shows the results of an examination in which the test greases of Examples 7A and 8A and Comparative Examples 22A and 23A were examined for bearing life in (Test 2) in Example A.
  • FIG. 5 is a graph which shows the results of a life test conducted in Example B.
  • FIG. 6 is a graph which shows the results of another life test conducted in Example B.
  • FIG. 7 is a graph which shows the results of still another life test conducted in Example B.
  • FIG. 8 is a graph which shows the results of Example C.
  • FIG. 9 is a graph which shows the results of Example D.
  • MODES FOR CARRYING OUT THE INVENTION
  • The invention will be explained below in detail.
  • (Lubricant Compositions)
  • One of the lubricant compositions of the invention includes a saturated fatty acid triglyceride as a lubricating ingredient and an antioxidant as an oxidation inhibitor.
  • The saturated fatty acid triglyceride is an ester of one or more saturated fatty acids with glycerol, and has biodegradability. The kinds of the saturated fatty acids are not particularly limited. However, linear fatty acids are preferred, and saturated fatty acids having 6-12 carbon atoms are preferred. In case where the saturated fatty acids each have 5 or less carbon atoms, there is the possibility that the base oil might have insufficient heat resistance. In case where the saturated fatty acids each have more than 12 carbon atoms, there is the possibility that the base oil might have too high a viscosity. Preferred of those are saturated fatty acids having 8-12 carbon atoms. Even more preferred are saturated fatty acids having 8-10 carbon atoms. Such saturated fatty acids have excellent lubricity and are available on the market at relatively low cost.
  • One saturated fatty acid triglyceride may be used alone, or a plurality of saturated fatty acid triglycerides may be used as a mixture thereof. Furthermore, the saturated fatty acid triglyceride may be either a saturated fatty acid triglyceride obtained by the reaction of three molecules of one saturated fatty acid with one molecule of glycerol or a saturated fatty acid triglyceride obtained by the reaction of three molecules, in total, of two or three saturated fatty acids with one molecule of glycerol.
  • In the case where a plurality of saturated fatty acid triglycerides are used as a mixture thereof, it is preferred that the mixture should be a mixture of a saturated fatty acid triglyceride which is an ester of a saturated fatty acid having 8 carbon atoms with glycerol (referred to as saturated fatty acid triglyceride A) and a saturated fatty acid triglyceride which is an ester of a saturated fatty acid having 10 carbon atoms with glycerol (referred to as saturated fatty acid triglyceride B). In this case, the molar ratio of the saturated fatty acid triglyceride A to the saturated fatty acid triglyceride B (A:B) is preferably in the range of 60:40 to 90:10, more preferably in the range of 70:30 to 80:20. When the molar ratio is regulated so as to be within such a range, the lubricant composition has better chemical performance, e.g., heat resistance and durability, and better mechanical performance, not to mention better low-torque characteristics.
  • In the case where a saturated fatty acid triglyceride obtained by the reaction of three molecules, in total, of two or three saturated fatty acids with one molecule of glycerol is used, it is preferred that this triglyceride should be a saturated fatty acid triglyceride obtained by the reaction of three molecules, in total, of a saturated fatty acid having 8 carbon atoms and a saturated fatty acid having 10 carbon atoms with one molecule of glycerol. In this case, the molar ratio of the saturated fatty acid ingredient having 8 carbon atoms (C) to the saturated fatty acid ingredient having 10 carbon atoms (D) (C:D) is preferably in the range of 60:40 to 90:10, more preferably in the range of 70:30 to 80:20. When the molar ratio is regulated so as to be within such a range, the lubricant composition has better chemical performance, e.g., heat resistance and durability, and better mechanical performance, not to mention better low-torque characteristics.
  • The molar ratio (C:D) can be regulated, for example, by mixing, in a suitable proportion, a saturated fatty acid triglyceride obtained by the reaction of one molecule of the saturated fatty acid having 8 carbon atoms and two molecules of the saturated fatty acid having 10 carbon atoms with one molecule of glycerol and a saturated fatty acid triglyceride obtained by the reaction of two molecules of the saturated fatty acid having 8 carbon atoms and one molecule of the saturated fatty acid having 10 carbon atoms with one molecule of glycerol.
  • It is preferred that the saturated fatty acid triglyceride should have a dynamic viscosity at 40° C. of 8-120 mm2/s. In case where the dynamic viscosity at 40° C. thereof is less than 8 mm2/s, there is the possibility that the base oil might have insufficient heat resistance. In case where the dynamic viscosity at 40° C. thereof exceeds 120 mm2/s, this base oil has increased shear resistance and there is the possibility that use of this lubricant composition in, for example, a rolling bearing might disadvantageously result in an increase in starting torque or rotation torque. From the standpoint of inhibiting such troubles from occurring, the dynamic viscosity at 40° C. of the saturated fatty acid triglyceride is more preferably 8-50 mm2/s, even more preferably 10-35 mm2/s, most preferably 10-20 mm2/s.
  • It is preferred that the lubricant composition should consist only of one or more saturated fatty acid triglycerides or contain one or more saturated fatty acid triglycerides as the main component. However, another kind of oil which is used as a base oil in general lubricants may be mixed with the saturated fatty acid triglyceride(s) so long as the oil is incorporated in such an amount that the objects of the invention are accomplished. For example, a natural lubricating oil such as an animal or vegetable oil is preferred. Examples thereof include beef tallow, lard, soybean oil, rapeseed oil, rice bran oil, coconut oil, palm oil, and palm kernel oil or products of hydrogenation of these.
  • The antioxidant may be an antioxidant which is in use as a food additive. Thus, the lubricant composition or the rolling device, e.g., a rolling bearing, that is equipped with the lubricant composition is rendered usable in machines for foods, machines for medicines, etc. Examples of such antioxidant include phenols, polyphenols, flavonoids, carotenoids, vitamins, vitamin analogues, and organic acids.
  • Examples of the phenols include BHA, butylhydroxytoluene (BHT), and TBHQ.
  • Examples of the polyphenols include grape seed extract, proanthocyanidin, and oil-soluble catechins.
  • Examples of the flavonoids include soybean isoflavone.
  • Examples of the cateroids include β-carotene, lycopene, and astaxanthin.
  • Examples of the vitamins include vitamin A substances, vitamin B substances, vitamin C substances, vitamin D substances, vitamin E substances, and vitamin K substances. Examples of the vitamin A substances include retinal, retinol, retinoic acid, and dehydroretinal. Examples of the vitamin B substances include thiamine, thiamine disulfide, dicethiamine, octotiamine, cycotiamine, bisibuthiamine, bisbentiamine, prosultiamine, benfotiamine, fursultiamine, riboflavin, flavin adenine dinucleotide, pyridoxine, pyridoxal, hydroxocobalamin, cyanocobalamin, methylcobalamin, deoxyadenocobalamin, folic acid, tetrahydrofolic acid, dihydrofolic acid, nicotinic acid, nicotinamide, nicotinyl alcohol, pantothenic acid, panthenol, biotin, choline, and inositol.
  • Examples of the vitamin C substances include ascorbic acid and derivatives thereof and erythorbic acid and derivatives thereof. Examples of the vitamin D substances include ergocalciferol, cholecalciferol, hydroxycholecalciferol, dihydroxycholecalciferol, and dihydrotachysterol. Examples of the vitamin E substances include tocopherols, derivatives thereof, and ubiquinone derivatives. The tocopherols are not particularly limited, and examples thereof include d-α-tocopherol, d-β-tocopherol, d-γ-tocopherol, d-δ-tocopherol, and dl-α-tocopherol. A mixture of these tocopherols may be used. Examples of the vitamin K substances include phytonadione, menaquinone, menadione, menadiol, an extract of fermented soybeans, and an extract of Bacillus natto. Examples of other vitamin substances include carnitine, ferulic acid, γ-orizanol, orotic acid, rutin, eriocitrin, and hesperidin.
  • Examples of the vitamin analogues include thioctic acid (α-liboic acid) and ubiquinol.
  • Examples of the organic acids include phytic acid.
  • One of these antioxidants may be used alone, or a suitable combination of two or more thereof may be used. To use two or more thereof in combination further enhances the effect of preventing oxidation.
  • The content of the antioxidant in the lubricant composition is an amount with which the effect of preventing oxidation can be imparted. The content thereof can be regulated in accordance with the kind of the lubricating ingredient, use, etc. For example, in the case of a grease composition to be enclosed in bearings, a sufficient oxidation-preventing effect is obtained by incorporating the antioxidant in an amount of 0.1-10% by mass based on the whole grease.
  • It is preferred to add a coenzyme Q to the lubricant composition, because the addition thereof further enhances the oxidation-preventing effect. Although the kind of the coenzyme Q is not particularly limited, coenzyme Q10 is especially preferred. One coenzyme Q may be used alone, or a suitable combination of two or more coenzymes Q may be used.
  • Furthermore, a thickener may be incorporated to produce a grease composition. Examples of the thickener include metal soaps such as aluminum soaps, barium soaps, calcium soaps, lithium soaps, sodium soaps, lithium complex soaps, calcium complex soaps, and aluminum complex soaps. Also usable are urea compounds such as diurea, triurea, tetraurea, and polyurea, urethane compounds, urea-urethane compounds, sodium terephthalamate, and the like. Moreover, gellants, such as amino acid-based gellants and polysaccharide esters, are also usable.
  • Furthermore, a dextrin fatty acid ester, which is obtained from a fatty acid and dextrin, or an inulin fatty acid ester, which is obtained from a fatty acid and inulin, can also be used as a thickener. Since these esters are materials derived from natural substances, the burden to be imposed on the environment is lessened. It is, however, noted that in the case where a dextrin fatty acid ester or an inulin fatty acid ester is used, various bacteria are apt to propagate and the grease composition is apt to be deteriorated by the propagation of bacteria. This bacterial deterioration of the grease composition can be inhibited by using, as an antioxidant, thioctic acid in combination with at least one member selected from vitamin E substances and polyphenols.
  • It is preferred that the fatty acids of the dextrin fatty acid ester and inulin fatty acid ester should be saturated fatty acids having 6-24 carbon atoms. Examples thereof include hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, dodecanoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid, heptadecanoic acid, octadecanoic acid, nanodecanoic acid, icosanoic acid, docosanoic acid, and tetradocosanoic acid. Preferred of these are pentadecanoic acid, hexadecanoic acid, and heptadecanoic acid. It is preferred that these saturated fatty acids should have a linear structure.
  • Incidentally, dextrin is a saccharide formed by polymerizing a plurality of α-glucose molecules through glycoside bonds, and is generally obtained by hydrolyzing a starch. Inulin also is a polysaccharide, and is designated as CAS No. 9005-8-5. Consequently, these substances exert no influence on the environment.
  • The amount of the thickener is not limited so long as the saturated fatty acid triglyceride can be thickened thereby, and the amount thereof can be suitably set in accordance with the desired worked consistency, torque, etc. However, the amount thereof is preferably 10-40% by mass based on the whole grease.
  • In the case where a grease composition is to be produced, it is also possible to use a saturated fatty acid triglyceride as a base oil and either magnesium stearate or calcium stearate as a thickener. It is preferred that the magnesium stearate and the calcium stearate to be used each should be of a food additive or medicine additive grade which meets standards such as the Japanese Standards for Food Additives or the Japanese Pharmacopoeia.
  • The content of the magnesium stearate or calcium stearate in the grease composition is not particularly limited. However, the content thereof is preferably 12-35% by mass. So long as the content thereof is within that range, the grease composition, when applied to a rolling device, can be inhibited from leaking out from the sliding part or rolling part. As a result, the rolling device can be lubricated over a long period. In case where the content thereof is less than 12% by mass, this grease composition has reduced shear stability and, hence, there is the possibility that this grease composition, when applied to a rolling device, might be softened by shearing in the sliding part or rolling part to accelerate the leakage of the grease composition from the sliding part or rolling part. As a result, there is the possibility that the rolling device cannot be lubricated over a long period. On the other hand, in case where the content of the thickener exceeds 35% by mass, the proportion of the base oil in the grease composition is low and, hence, there is the possibility that this grease composition might have insufficient lubricity. From the standpoint of inhibiting such troubles from occurring, the content of the thickener in the grease composition is more preferably 12-28% by mass, even more preferably 12-25% by mass, most preferably 15-25% by mass.
  • Additives which are in general use in lubricants may be further added to the lubricant composition in order to further improve the various performances of the lubricant composition. Examples thereof include rust preventives, extreme-pressure agents, friction regulators, pH regulators, antiwear agents, oiliness improvers, and metal deactivators. However, additives which contain a metallic element are undesirable from the standpoint of the environment. One of those additives may be used alone, or a suitable combination of two or more thereof may be used. The total content of the additives in the lubricant composition is not particularly limited unless the additives defeat the objects of the invention.
  • (Rolling Device)
  • The rolling device of the invention is lubricated with the lubricant composition or grease composition described above. There are no limitations on the kind of the rolling device. Examples thereof include deep-groove ball bearings such as that shown in FIG. 1. The deep-groove ball bearing shown in the figure is equipped with: an inner ring 1 which has a raceway surface 1 a in the outer circumferential surface thereof; an outer ring 2 which has, in the inner circumferential surface thereof, a raceway surface 2 a that faces the raceway surface la and which has been disposed radially outside the inner ring 1; a plurality of rolling elements (balls) 3 which have been disposed between the two raceway surfaces 1 a and 2 a so as to be freely rollable; a cage 4 which holds the multiple rolling elements 3 between the inner ring 1 and the outer ring 2; and sealing devices 5 and 5 which serve as seals that close the space openings present between the inner ring 1 and the outer ring 2. Incidentally, the cage 4 and the sealing devices 5 may be omitted.
  • The grease composition described above is filled into the space (bearing space) which has been formed between the inner ring 1 and the outer ring 2 and in which the rolling elements 3 have been disposed, in order to lubricate between each raceway surface 1 a or 2 a and the rolling elements 3. Consequently, the rolling device of the invention has excellent durability and exerts little influence on the environment.
  • Incidentally, the embodiment shown is a mere example of the invention, and the invention should not be construed as being limited to the embodiment. For example, the invention can be applied to other rolling bearings of various kinds The invention is applicable to radial rolling bearings such as angular ball bearings, self-aligning ball bearings, cylindrical roller bearings, tapered roller bearings, needle roller bearings, and self-aligning roller bearings and thrust rolling bearings such as thrust ball bearings and thrust roller bearings. Applications of the invention are not limited to such rolling bearings, and the invention is further applicable to other rolling devices of various kinds, such as, for example, ball screws, direct-acting guides, and direct-acting bearings.
  • EXAMPLES
  • The invention will be further explained below by reference to Examples and Comparative Examples. However, the invention should not be construed as being limited by the Examples.
  • Example A (Test 1: Examples 1A to 3A and Comparative Examples 1A to 19A)
  • Thioctic acid (α-LI), d-α-tocopherol (V.E.), catechin (Kat), dibutylhydroxytoluene (BHT), isoflavone (IF), β-carotene (Car), and butylhydroxyanisole (BHA) were added alone or in combination as shown in Table 1 to a saturated medium-chain fatty acid triglyceride (“Panasate 875”, manufactured by NOF Corp.) to prepare test lubricating oils. The addition amounts of those antioxidants were as follows. When an antioxidant compound was used alone, the compound was added in an amount of 2.5% by mass. When a mixture of two antioxidant compounds was used, each compound was added in an amount of 1.25% by mass, the total amount thereof being 2.5% by mass.
  • TABLE 1
    Example 1A Example 2A Example 3A
    α-LI α-LI α-LI
    V.E. Kat
    Comparative Comparative Comparative Comparative
    Example 1A Example 2A Example 3A Example 4A
    BHT V.E. IF Kat
    BHT BHT BHT
    Comparative Comparative Comparative Comparative
    Example 5A Example 6A Example 7A Example 8A
    Car BHA V.E. IF
    BHT BHT V.E.
    Comparative Comparative Comparative Comparative
    Example 9A Example 10A Example 11A Example 12A
    Car BHA IF Car
    V.E. V.E. IF
    Comparative Comparative Comparative Comparative
    Example 13A Example 14A Example 15A Example 16A
    BHA Kat Car BHA
    IF Kat Kat
    Comparative Comparative Comparative
    Example 17A Example 18A Example 19A
    Car BHA BHA
    Car
    BHT: dibutylhydroxytoluene
    V.E.: d-α-tocopherol
    IF: isoflavone
    Kat: catechin
    Car: β-carotene
    α-LI: thioctic acid
    BHA: butylhydroxyanisole
  • Forty grams of each test lubricating oil was placed on a stainless-steel petri dish and heated in a 160° C. oven. The viscosity of the test lubricating oil was measured after a given period had passed, and the increase in viscosity from the value measured before the heating was determined. The results thereof are shown in FIG. 2. The test lubricating oils of Examples 1A to 3A contained thioctic acid alone or contained a mixture of thioctic acid with catechin or d-α-tocopherol. It can be seen that these lubricating oils were inhibited from suffering an increase in viscosity due to heating.
  • (Test 2: Examples 4A to 8A and Comparative Examples 20A to 23A)
  • Thioctic acid, catechin, d-α-tocopherol, butylhydroxyanisole (BHA), dibutylhydroxytoluene (BHT), or phenyl-α-naphthylamine (PAN) was added to base greases each including both a base oil and a thickener, as shown in Table 2, to prepare test greases. As the base oil was used a saturated medium-chain fatty acid triglyceride (MCT) or a polyol ester oil. As the thickener, use was made of dextrin hexadecanoate, lithium 12-hydroxystearate, or a product of reaction between stearylamine and 4,4′-diphenylmethane diisocyanate (C18-MDI urea). The amounts of the thickeners in the base greases were 15% by mass for dextrin hexadecanoate, 12% by mass for lithium 12-hydroxystearate, and 15% by mass for the urea. Thus, the base greases had been regulated so as to have the shown consistency values.
  • TABLE 2
    Kind
    Viscosity of
    of base oil Consistency Base
    Thickener (mm2/s, at 40° C.) unworked worked oil Composition of additive
    Example 4A dextrin 12.8 248 290 MCT thioctic acid, 2.5 mass %
    hexadecanoate
    Example 5A dextrin 12.8 262 290 MCT thioctic acid, 1.25 mass % +
    hexadecanoate catechin, 1.25 mass %
    Example 6A dextrin 12.8 262 292 MCT thioctic acid, 1.25 mass % +
    hexadecanoate d-α-tocopherol, 1.25 mass %
    Example 7A lithium 32.0 252 264 polyol thioctic acid, 1.25 mass % +
    12-hydroxystearate ester catechin, 1.25 mass %
    Example 8A C18-MDI urea 32.0 252 274 polyol thioctic acid, 1.25 mass % +
    ester catechin, 1.25 mass %
    Comparative dextrin 12.8 255 286 MCT BHA, 2.5 mass %
    Example 20A hexadecanoate
    Comparative dextrin 12.8 258 290 MCT BHA, 1.25 mass % +
    Example 21A hexadecanoate BHT, 1.25 mass %
    Comparative lithium 32.0 256 268 polyol BHT, 1.25 mass % +
    Example 22A 12-hydroxystearate ester PAN, 1.25 mass %
    Comparative C18-MDI urea 32.0 250 270 polyol BHT, 1.25 mass % +
    Example 23A ester PAN, 1.25 mass %
    C18-MDI urea: product of reaction between stearylamine and 4,4′-diphenylmethane diisocyanate
    MCT: saturated middle-chain fatty acid triglyceride
    BHA: butylhydroxyanisole
    BHT: dibutylhydroxytoluene
    PAN: phenyl-α-naphthylamine
  • Thereafter, 3.4 g of each test grease was enclosed in bearing “6305VVC3E”, manufactured by NSK Ltd., and the bearing was rotated under the conditions 1 and conditions 2 shown in Table 3 to determine the life. This test was conducted twice under each set of conditions.
  • TABLE 3
    Rotation Grease Ambient
    Axial speed amount temperature
    Bearing load (N) (rpm) (g) (° C.)
    Conditions 1 6305VVC3E 198 15,000 3.4 80
    Conditions 2 6305VVC3E 198 10,000 3.4 120
  • The results obtained under the conditions 1 are shown in FIG. 3, and the results obtained under the conditions 2 are shown in FIG. 4. It can be seen that the addition of thioctic acid alone or a mixture of thioctic acid and either catechin or d-α-tocopherol enhanced high-temperature durability and resulted in a prolongation of life, as in Examples 4A to 8A. In particular, as shown in FIG. 4, these antioxidants even at the high temperature showed a higher oxidation-preventing effect and brought about longer lives than the phenol/amine combination, which has conventionally been used as an industrial additive. Furthermore, such performance of the antioxidants according to the invention changed little when the base oil or the thickener changed.
  • Example B
  • Test greases were prepared in accordance with the formations shown in
  • Table 4.
  • TABLE 4
    Worked Unworked
    Consis- Consis-
    Thickener Base oil Antioxidant tency tency
    Example 1B aluminum complex soap MCT dl-α-tocopherol 292 262
    Example 2B dextrin palmitate MCT d-α-tocopherol 286 260
    Example 3B dextrin palmitate MCT d-α-tocopherol + 286 258
    d-δ-tocopherol
    Example 4B urea compound MCT d-δ-tocopherol 198 178
    Comparative lithium polyol ester oil dl-α-tocopherol 187 174
    Example 1B 12-hydroxystearate
    Comparative aluminum complex soap MCT dl-α-tocopherol 289 258
    Example 2B
    Comparative dextrin palmitate MCT d-α-tocopherol 291 266
    Example 3B
    Comparative dextrin palmitate MCT d-α-tocopherol + 286 248
    Example 4B d-δ-tocopherol
    Comparative urea compound MCT d-δ-tocopherol 198 178
    Example 5B
    Comparative dextrin palmitate rapeseed oil d-δ-tocopherol 250 230
    Example 6B
    Comparative dextrin palmitate rapeseed oil d-α-tocopherol + 248 225
    Example 7B d-δ-tocopherol
  • The grease of Example 1B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa·s as a base oil and an aluminum complex soap as a thickener, and which had been obtained by adding an antioxidant and coenzyme Q10 to the base oil and thickener in an amount of 2.5% by mass each. The kind of the antioxidant added was dl-α-tocopherol as shown in Table 4.
  • The grease of Example 2B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa·s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant and coenzyme Q10 to the base oil and thickener in an amount of 2.5% by mass each. The kind of the antioxidant added was d-α-tocopherol as shown in Table 4.
  • The grease of Example 3B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa·s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant and coenzyme Q10 to the base oil and thickener in an amount of 2.5% by mass each. The kind of the antioxidant added was a natural type vitamin E which was on the market as a mixture of d-α-tocopherol and d-δ-tocopherol, as shown in Table 4.
  • The grease of Example 4B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa·s as a base oil and a urea compound as a thickener, and which had been obtained by adding an antioxidant and coenzyme Q10 to the base oil and thickener in an amount of 2.5% by mass each. The kind of the antioxidant added was d-δ-tocopherol as shown in Table 4. The urea compound was a compound synthesized by reacting 1 mol of diphenylmethane 4,4′-diisocyanate (MDI) with 2 mol of stearylamine.
  • Incidentally, the amount of the thickener added in each of Examples 1B to 4B was 12% by mass. The values of worked consistency and unworked consistency of these test greases were as shown in Table 4.
  • The grease of Comparative Example 1B was a grease which included a polyol ester oil having a dynamic viscosity at 40° C. of 32.6 mPa·s as a base oil and lithium 12-hydroxystearate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass. The kind of the antioxidant added was dl-α-tocopherol as shown in Table 4.
  • The grease of Comparative Example 2B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa·s as a base oil and an aluminum complex soap as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass. The kind of the antioxidant added was dl-α-tocopherol as shown in Table 4.
  • The grease of Comparative Example 3B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa·s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass. The kind of the antioxidant added was d-α-tocopherol as shown in Table 4.
  • The grease of Comparative Example 4B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa·s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass. The kind of the antioxidant added was a natural type vitamin E which was on the market as a mixture of d-α-tocopherol and d-δ-tocopherol, as shown in Table 4.
  • The grease of Comparative Example 5B was a grease which included a medium-chain fatty acid triglyceride (MCT) having a dynamic viscosity at 40° C. of 12.8 mPa·s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass. The kind of the antioxidant added was d-δ-tocopherol as shown in Table 4. The urea compound was a compound synthesized by reacting 1 mol of diphenylmethane 4,4′-diisocyanate (MDI) with 2 mol of stearylamine.
  • The grease of Comparative Example 6B was a grease which included rapeseed oil having a dynamic viscosity at 40° C. of 32 mPa·s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass. The kind of the antioxidant added was d-δ-tocopherol as shown in Table 4.
  • The grease of Comparative Example 7B was a grease which included rapeseed oil having a dynamic viscosity at 40° C. of 32 mPa·s as a base oil and dextrin palmitate as a thickener, and which had been obtained by adding an antioxidant to the base oil and thickener in an amount of 5% by mass. The kind of the antioxidant added was a natural type vitamin E which was on the market as a mixture of d-α-tocopherol and d-δ-tocopherol, as shown in Table 4.
  • Incidentally, the amount of the thickener added in each of Comparative Examples 1B to 7B was 12% by mass. The values of worked consistency and unworked consistency of these test greases were as shown in Table 4. Comparative Examples 2B, 3B, 4B, and 5B are Reference Examples for ascertaining the effect of the coenzyme Q.
  • [Life Test]
  • With respect to the test greases of Example 1B and Comparative Examples 1B and 2B, 3.4 g of each test grease was enclosed in rolling bearing No. 6305VVC3E, and this rolling bearing was rotated under the conditions of an ambient temperature of 120° C., an axial load of 98 N, and a rotation speed of 10,000 min−1. The period required for the driving motor for rotating the rolling bearing to stop due to overload was measured, and this period was taken as the life.
  • With respect to the test greases of Examples 2B to 4B and Comparative Examples 3B to 5B, 1.0 g of each test grease was enclosed in rolling bearing No. 6303VVC3E, and this rolling bearing was rotated under the conditions of an ambient temperature of 80° C., a radial load of 198 N, and a rotation speed of 24,000 min−1. The period required for the driving motor for rotating the rolling bearing to stop due to overload was measured, and this period was taken as the life.
  • Furthermore, with respect to the test greases of Comparative Examples 6B and 7B, 1.0 g of each test grease was enclosed in rolling bearing No. 6303VVC3E, and this rolling bearing was rotated under the conditions of an ambient temperature of 80° C., a radial load of 198 N, and a rotation speed of 24,000 min−1. The period required for the driving motor for rotating the rolling bearing to stop due to overload was measured, and this period was taken as the life.
  • Incidentally, the life test was conducted twice for each test grease. The results thereof are shown as graphs in FIGS. 5 to 7. As can be seen from the graphs given in FIGS. 5 to 7, the Examples, in which the test greases each contained coenzyme Q10, attained a longer life than the Comparative Examples, in which the test greases did not contain coenzyme Q10.
  • Example C Example 1C
  • Eighty-five grams of a saturated medium-chain fatty acid triglyceride having a dynamic viscosity at 40° C. of 14.8 mm2/s (Panasate 875, manufactured by NOF Corp.) was mixed with 15 g of magnesium stearate, and this mixture was heated, with stirring, to a temperature at which the magnesium stearate dissolved. After the magnesium stearate had dissolved completely, the solution was poured into an aluminum vat which had been cooled beforehand. This vat was cooled with flowing water. The mixture which had become greasy was kneaded with a three-roll mill to obtain a test grease. This test grease had a value of worked consistency of 300.
  • Comparative Example 1C
  • Eighty-eight grams of a saturated medium-chain fatty acid triglyceride having a dynamic viscosity at 40° C. of 14.8 mm2/s (Panasate 875, manufactured by NOF Corp.) was mixed with 12 g of lithium 12-hydroxystearate, and this mixture was heated, with stirring, to a temperature at which the lithium 12-hydroxystearate dissolved. After the lithium 12-hydroxystearate had dissolved completely, the solution was poured into an aluminum vat which had been cooled beforehand. This vat was cooled with flowing water. The mixture which had become greasy was kneaded with a three-roll mill to obtain a test grease. This test grease had a value of worked consistency of 231.
  • Comparative Example 2C
  • Eighty-eight grams of a polyol ester oil having a dynamic viscosity at 40° C. of 26.0 mm2/s was mixed with 12 g of lithium 12-hydroxystearate, and this mixture was heated, with stirring, to a temperature at which the lithium 12-hydroxystearate dissolved. After the lithium 12-hydroxystearate had dissolved completely, the solution was poured into an aluminum vat which had been cooled beforehand. This vat was cooled with flowing water. The mixture which had become greasy was kneaded with a three-roll mill to obtain a test grease. This test grease had a value of worked consistency of 250.
  • [Rotation Torque Test]
  • Each of the test greases thus produced was filled, in an amount of 1.0 g, into the bearing space of deep-groove ball bearing No. 6203VV (inner diameter, 17 mm; outer diameter, 40 mm). Thus, three test bearings were obtained. These test bearings were subjected to a rotation test at various rotation speeds (1,800-7,500 min−1) and examined for rotation torque. The axial load was set at 196 N, and the test temperature was room temperature.
  • The rotation torque was measured throughout the period from the time when 550 seconds had passed since the initiation of rotation to the time when 600 seconds had passed since the rotation initiation, and the average value thereof was taken as the rotation torque of this test bearing. The results thereof are shown as a graph in FIG. 8. The abscissa of the graph in FIG. 8 is the value of dmN determined from the rotation speed during the test. As can be seen from the graph given in FIG. 8, the test bearing equipped with the test grease of Example 1C showed excellent low-torque characteristics at each rotation speed as compared with the test bearings equipped with the test greases of Comparative Examples 1C and 2C.
  • Example D Example 1D
  • Eighty-five grams of a saturated medium-chain fatty acid triglyceride having a dynamic viscosity at 40° C. of 14.8 mm2/s (Panasate 875, manufactured by NOF Corp.) was mixed with 15 g of calcium stearate, and this mixture was heated, with stirring, to a temperature at which the calcium stearate dissolved. After the calcium stearate had dissolved completely, the solution was poured into an aluminum vat which had been cooled beforehand. This vat was cooled with flowing water. The mixture which had become greasy was kneaded with a three-roll mill to obtain a test grease. This test grease had a value of worked consistency of 230.
  • Comparative Example 1D
  • Eighty-eight grams of a saturated medium-chain fatty acid triglyceride having a dynamic viscosity at 40° C. of 14.8 mm2/s (Panasate 875, manufactured by NOF Corp.) was mixed with 12 g of lithium 12-hydroxystearate, and this mixture was heated, with stirring, to a temperature at which the lithium 12-hydroxystearate dissolved. After the lithium 12-hydroxystearate had dissolved completely, the solution was poured into an aluminum vat which had been cooled beforehand. This vat was cooled with flowing water. The mixture which had become greasy was kneaded with a three-roll mill to obtain a test grease. This test grease had a value of worked consistency of 231.
  • Comparative Example 2D
  • Eighty-eight grams of a polyol ester oil having a dynamic viscosity at 40° C. of 26.0 mm2/s was mixed with 12 g of lithium 12-hydroxystearate, and this mixture was heated, with stirring, to a temperature at which the lithium 12-hydroxystearate dissolved. After the lithium 12-hydroxystearate had dissolved completely, the solution was poured into an aluminum vat which had been cooled beforehand. This vat was cooled with flowing water. The mixture which had become greasy was kneaded with a three-roll mill to obtain a test grease. This test grease had a value of worked consistency of 250.
  • [Rotation Torque Test]
  • A rotation torque test was conducted in the same manner as in Example C. The results thereof are shown as a graph in FIG. 9. The abscissa of the graph in FIG. 9 is the value of dmN determined from the rotation speed during the test. As can be seen from the graph given in FIG. 9, the test bearing equipped with the test grease of Example 1D showed excellent low-torque characteristics at each rotation speed as compared with the test bearings equipped with the test greases of Comparative Examples 1D and 2D.
  • While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.
  • This application is based on a Japanese patent application filed on Jun. 15, 2011 (Application No. 2011-133118), a Japanese patent application filed on Nov. 30, 2011 (Application No. 2011-262944), and a Japanese patent application filed on Nov. 30, 2011 (Application No. 2011-262945), the contents thereof being incorporated herein by reference.
  • INDUSTRIAL APPLICABILITY
  • The lubricant compositions and rolling device of the invention are useful in or as the rotating parts or sliding parts of various machines and apparatus. The lubricant compositions are harmless even when eaten, and impose little burden on the environment. Consequently, the lubricant compositions and the rolling device are useful especially in machines and apparatus which relate to foods or medical supplies.
  • DESCRIPTION OF REFERENCE NUMERALS AND SIGNS
    • 1 Inner ring
    • 1 a Raceway surface
    • 2 Outer ring
    • 2 a Raceway surface
    • 3 Rolling element
    • G Lubricant composition

Claims (12)

1-6. (canceled)
7. A lubricant composition which comprises a saturated fatty acid triglyceride and an antioxidant.
8. The lubricant composition as claimed in claim 7, wherein the antioxidant comprises at least one member selected from phenols, polyphenols, flavonoids, carotenoids, vitamins, vitamin analogues, and organic acids.
9. The lubricant composition as claimed in claim 7 or 8, which contains a coenzyme Q.
10. The lubricant composition as claimed in claim 7 or 8, which contains a fatty acid ester, a metal soap, or a urea compound as a thickener.
11. The lubricant composition as claimed in claim 9, which contains a fatty acid ester, a metal soap, or a urea compound as a thickener.
12. A lubricant composition which comprises a saturated fatty acid triglyceride as a base oil and either magnesium stearate or calcium stearate as a thickener.
13. A rolling device equipped with an inner member which has a raceway surface in the outer surface thereof, an outer member which has a raceway surface that faces the raceway surface of the inner member and which has been disposed outside the inner member, a plurality of rolling elements which have been disposed between the two raceway surfaces so as to be freely rollable, and a lubricant which lubricates between each raceway surface and the rolling elements, wherein the lubricant is the lubricant composition according to claim 7 or 8.
14. A rolling device equipped with an inner member which has a raceway surface in the outer surface thereof, an outer member which has a raceway surface that faces the raceway surface of the inner member and which has been disposed outside the inner member, a plurality of rolling elements which have been disposed between the two raceway surfaces so as to be freely rollable, and a lubricant which lubricates between each raceway surface and the rolling elements, wherein the lubricant is the lubricant composition according to claim 9.
15. A rolling device equipped with an inner member which has a raceway surface in the outer surface thereof, an outer member which has a raceway surface that faces the raceway surface of the inner member and which has been disposed outside the inner member, a plurality of rolling elements which have been disposed between the two raceway surfaces so as to be freely rollable, and a lubricant which lubricates between each raceway surface and the rolling elements, wherein the lubricant is the lubricant composition according to claim 10.
16. A rolling device equipped with an inner member which has a raceway surface in the outer surface thereof, an outer member which has a raceway surface that faces the raceway surface of the inner member and which has been disposed outside the inner member, a plurality of rolling elements which have been disposed between the two raceway surfaces so as to be freely rollable, and a lubricant which lubricates between each raceway surface and the rolling elements, wherein the lubricant is the lubricant composition according to claim 11.
17. A rolling device equipped with an inner member which has a raceway surface in the outer surface thereof, an outer member which has a raceway surface that faces the raceway surface of the inner member and which has been disposed outside the inner member, a plurality of rolling elements which have been disposed between the two raceway surfaces so as to be freely rollable, and a lubricant which lubricates between each raceway surface and the rolling elements, wherein the lubricant is the lubricant composition according to claim 12.
US13/580,485 2011-06-15 2012-01-23 Lubricant compositions and rolling device Abandoned US20130116158A1 (en)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
JP2011133118A JP2012126880A (en) 2010-11-24 2011-06-15 Lubricant composition and rolling apparatus
JP2011-133118 2011-06-15
JP2011-262944 2011-11-30
JP2011-262945 2011-11-30
JP2011262945 2011-11-30
JP2011262944 2011-11-30
PCT/JP2012/051322 WO2012172824A1 (en) 2011-06-15 2012-01-23 Lubricant composition and rolling device

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160145522A1 (en) * 2013-06-12 2016-05-26 Nsk Ltd. Grease composition and rolling bearing

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6093992B2 (en) * 2013-05-24 2017-03-15 日清オイリオグループ株式会社 Grease spray for food machine and method for producing grease spray for food machine
CN104178322A (en) * 2013-05-27 2014-12-03 天津市泽畅科技有限公司 Engine oil deposit control agent
CN104178278A (en) * 2013-05-27 2014-12-03 天津市泽畅科技有限公司 Deposit control additive for lubricating oil
CN104178281A (en) * 2013-05-27 2014-12-03 天津市泽畅科技有限公司 Engine oil deposit control additive
JP2014240467A (en) * 2013-06-12 2014-12-25 日本精工株式会社 Grease composition and rolling bearing
JP2015021053A (en) * 2013-07-18 2015-02-02 日本精工株式会社 Grease composition and rolling device with the same encapsulated therein
JP2015021057A (en) * 2013-07-18 2015-02-02 日本精工株式会社 Grease composition and rolling device enclosing it
JP6334377B2 (en) * 2014-12-03 2018-05-30 株式会社日立製作所 Elevator rope oil, grease for elevator rope, elevator rope and traction type elevator
CN104531271A (en) * 2014-12-04 2015-04-22 曲建勋 Preparation process for pure plant oil additive
CN106085573A (en) * 2016-06-23 2016-11-09 安徽中天石化股份有限公司 A kind of environmental type grease
CN107573996A (en) * 2017-09-18 2018-01-12 吴江华威特种油有限公司 A kind of wear resistence lubricating oil and preparation method thereof
JP2020059793A (en) * 2018-10-09 2020-04-16 オリンパス株式会社 Lubricant for medical equipment and medical equipment

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5773391A (en) * 1994-11-15 1998-06-30 The Lubrizol Corporation High oleic polyol esters, compositions and lubricants, functional fluids and greases containing the same
US20020142920A1 (en) * 2000-11-06 2002-10-03 Nsk Ltd. Lubricating grease compositon and rolling apparatus
JP2010241858A (en) * 2009-04-01 2010-10-28 Nsk Ltd Lubricant composition and rolling device

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB934892A (en) * 1961-04-07 1963-08-21 British Petroleum Co Greases having anti-corrosion properties
JP2909650B2 (en) 1990-07-13 1999-06-23 月島食品工業株式会社 Lubricating oil composition for chainsaws
JP3207535B2 (en) * 1992-08-07 2001-09-10 森永乳業株式会社 Antioxidant
US6547986B1 (en) 2000-09-21 2003-04-15 Lord Corporation Magnetorheological grease composition
JP2002323053A (en) 2001-04-26 2002-11-08 Nsk Ltd Rolling bearing
JP2007064456A (en) 2005-09-02 2007-03-15 Ntn Corp Rolling bearing for robot
DE112007002582T5 (en) * 2006-11-09 2009-11-12 Ntn Corp. Greased bearing for inverter drive motor
JP2008248990A (en) 2007-03-29 2008-10-16 Nippon Oil Corp Lubricating method of rolling guide surface
JP4730714B2 (en) 2008-08-28 2011-07-20 日産自動車株式会社 Grease composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5773391A (en) * 1994-11-15 1998-06-30 The Lubrizol Corporation High oleic polyol esters, compositions and lubricants, functional fluids and greases containing the same
US20020142920A1 (en) * 2000-11-06 2002-10-03 Nsk Ltd. Lubricating grease compositon and rolling apparatus
JP2010241858A (en) * 2009-04-01 2010-10-28 Nsk Ltd Lubricant composition and rolling device

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160145522A1 (en) * 2013-06-12 2016-05-26 Nsk Ltd. Grease composition and rolling bearing

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EP2722384A4 (en) 2015-04-22

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