Technical Field
[0001] The present invention relates to a grease composition capable of reducing an amount
of wear in sliding parts.
Background Art
[0002] Grease has been mainly used for slide bearings and rolling bearings (bearings), or
for sliding surfaces where a lubricant film cannot easily remain attached because
of moving contact surfaces. Typically, grease is prepared by mixing a thickening agent,
and, as required, additives, to a lubricant base oil.
[0003] With the advancement in machine technology such as in automobiles and electrical
devices, these devices are used in increasing severe operating conditions as the trend
for downsizing and lighting, higher output, and longer life continues to grow. This
has increased the demand for higher performance, for example, lubricity, in greases
used for these devices.
[0004] Various options are proposed for the base oil, thickening agent, and additives to
improve grease lubricity. For example, it has been proposed to add an amide compound
and a solid lubricant to improve grease lubricity, for example, such as abrasion resistance
(see PTL 1, and PTL 2). However, a grease having better lubricity is needed.
[0005] Hydroxyfatty acid metal salts are used as thickening agents for grease (see, for
example, PTL 3). However, the hydroxyfatty acid metal salts used as thickening agents
are mostly lithium 12-hydroxystearate, and an α- or ω-hydroxyfatty acid metal salt
is not used. It is also known that use of this type of compound as an grease additive
results in a shorter life, though it improves antirust performance (for example, PTL
4).
Citation List
Patent Literature
Summary of Invention
Technical Problem
[0007] The present invention was made under these circumstances, and it is an object of
the present invention to provide a grease composition that is capable of reducing
an amount of wear in sliding parts of various members of automobiles, electrical devices,
and the like.
Solution to Problem
[0008] The present inventors diligently worked to achieve the foregoing object, and found
that an amount of wear can be greatly reduced by the synergy between metal salts of
specific hydroxycarboxylic acids and an amide compound. The present invention was
completed on the basis of this finding, and includes the following.
[0009]
- (1) A grease composition comprising:
a lubricant base oil;
a thickening agent;
an amide compound; and
at least one of an α-hydroxycarboxylic acid metal salt, and an ω-hydroxycarboxylic
acid metal salt,
wherein the hydroxycarboxylic acid metal salts are contained in a total content of
0.1 to 2 mass% with respect to a total amount of the grease composition.
- (2) The grease composition according to item (1), wherein the hydroxycarboxylic acid
metal salt is an alkali metal salt, or an alkali earth metal salt.
- (3) The grease composition according to item (2), wherein the hydroxycarboxylic acid
metal salt is a calcium salt, or a barium salt.
- (4) The grease composition according to any one of items (1) to (3), wherein the hydroxycarboxylic
acid is a monovalent hydroxycarboxylic acid of 8 to 24 carbon atoms.
- (5) The grease composition according to any one of items (1) to (4), wherein the thickening
agent contains at least one of a urea-based thickening agent, and a metal soap-based
thickening agent.
- (6) The grease composition according to any one of items (1) to (5), which further
comprises a solid lubricant component.
- (7) A lubrication method comprising using the grease composition of any one of items
(1) to (6) at a sliding part.
Advantageous Effects of Invention
[0010] The grease composition of the present invention is highly effective at greatly reducing
wear in sliding parts of various members of automobiles, electrical devices, and the
like.
Description of Embodiments
Lubricant Base Oil
[0011] A lubricant base oil of the present invention may be a mineral or a synthetic lubricant
base oil, as long as it is a lubricant base oil commonly used for grease. The lubricant
base oil has a kinetic viscosity at 40°C of preferably 1 to 500 mm
2/s, more preferably 5 to 100 mm
2/s. A grease composition having desirable consistency can be prepared with ease when
the kinetic viscosity at 40°C is 1 to 500 mm
2/s. In order to prepare a grease having excellent lubricity, it is preferable to use
a lubricant base oil of physical properties with a viscosity index of 90 or more,
particularly 95 to 250, a pour point of -10°C or less, particularly -15 to -70°C,
and a flash point of 150°C or more.
[0012] When containing a solid lubricant, the lubricant base oil preferably has a density
of 0.75 to 0.95 g/cm
3 at a lubricant base oil temperature of 15°C. The density is particularly preferably
0.8 to 0.9 g/cm
3.
[0013] The mineral lubricant base oil may be a lubricant oil fraction obtained through purification
of a distillate oil by various purification processes after distillation of a crude
oil under ordinary pressure or under ordinary pressure and reduced pressure. The purification
processes include, for example, hydrorefining, solvent extraction, solvent dewaxing,
hydrodewaxing, sulfuric acid washing, and clay treatment. The base oil of the present
invention can be obtained from a combination of these processes performed in appropriate
order. A mixture of different refined oils of different qualities obtained by treating
different crude oils or different distillate oils with a combination of different
processes in different order is also useful. Regardless of the method, the base oil
can be desirably used when the base oil quality is adjusted to satisfy the foregoing
density.
[0014] The synthetic lubricant base oil uses preferably a base material having desirable
hydrolytic stability. Examples of such base materials include polyolefins such as
poly-α-olefins, polybutene, and a copolymer of two or more olefins; polyesters, polyalkylene
glycols, alkylbenzenes, and alkylnaphthalenes. Poly-α-olefins are preferred for availability,
cost, viscosity characteristics, oxidation stability, and compatibility with system
components. Further preferred for cost are poly-α-olefins made by polymerizing olefins
such as 1-dodecene, and 1-decene.
[0015] Also preferred as the synthetic lubricant base oil are ester-based base oils, for
example, such as a polyolester of a polyalcohol and a monovalent carboxylic acid,
and a diester of a divalent carboxylic acid and an alcohol. Preferred are polyolesters
obtained from a polyalcohol selected from neopentyl glycol, trimethylolpropane, and
pentaerythritol, and a fatty acid of 4 to 22 carbon atoms. The fatty acid is particularly
preferably a fatty acid of 12 to 20 carbon atoms, particularly an unsaturated fatty
acid.
[0016] The lubricant base oil may use base oils other than the poly-α-olefinic base oil
and the ester-based base oil. It is, however, preferable to contain 80 mass% or more,
particularly 90 mass% or more of the poly-α-olefin or ester-based base oil with respect
to the mass of the lubricant base oil.
[0017] The synthetic lubricant base oil may be used alone or as a mixture of two or more.
It is also possible to use the synthetic lubricant base oil as a mixture with the
mineral base oil.
[0018] The content of the lubricant base oil is preferably 50 to 95 mass%, particularly
preferably 60 to 85 mass% with respect to the total amount of the grease composition.
A grease composition having desirable consistency can be prepared with ease when the
lubricant base oil content is 50 to 95 mass%.
Thickening Agent
[0019] A thickening agent commonly used for grease may be used as the thickening agent of
the present invention without causing trouble. It is, however, preferable to use a
metal soap-based thickening agent, or a urea-based thickening agent. The thickening
agent may be used alone or as a mixture of two or more. The thickening agent may be
contained in any amount, as long as the desired consistency is obtained. For example,
the thickening agent content is preferably 2 to 30 mass%, further preferably 5 to
20 mass% with respect to the total amount of the grease composition.
[0020] The metal soap-based thickening agent is a thickening agent of a carboxylic acid
metal salt. The carboxylic acid may be a derivative of carboxylic acids having a hydroxy
group.
[0021] The carboxylic acids may be aliphatic carboxylic acids such as stearic acid, and
azelaic acid, or aromatic carboxylic acids such as terephthalic acid. Monovalent or
divalent aliphatic carboxylic acids, particularly aliphatic carboxylic acids of 6
to 20 carbon atoms are used. Particularly preferred for use are monovalent aliphatic
carboxylic acids of 12 to 20 carbon atoms, and divalent aliphatic carboxylic acids
of 6 to 14 carbon atoms. Monovalent aliphatic carboxylic acids having one hydroxyl
group are preferred.
[0022] The metal may be an alkali metal such as lithium and sodium, an alkali earth metal
such as calcium, or an amphoteric metal such as aluminum. Preferred are alkali metals,
particularly lithium.
[0023] Metal salts of α- or ω-hydroxyfatty acids are not preferred as thickening agents
because of poor thickening capability.
[0024] The thickening agent may be added in the form of a metal soap, or as a metal-soap
thickening agent by separately adding the carboxylic acid and a metal source (e.g.,
a metal salt, a metal salt hydroxide), and causing these to react at the time of grease
production.
[0025] The carboxylic acid metal salt may be used alone or as a mixture of two or more.
For example, a mixture of lithium 12-hydroxystearate and lithium azelate is particularly
preferred.
[0026] The urea-based thickening agent may be, for example, a diurea compound obtained by
a reaction of a diisocyanate and a monoamine, or a polyurea compound obtained by a
reaction of a diisocyanate with a monoamine or a diamine.
[0027] Diisocyanates are compounds in which two of the hydrogen atoms of the hydrocarbon
are substituted with isocyanate groups. Preferred examples of the diisocyanates include
phenylene diisocyanate, tolylene diisocyanate, diphenyl diisocyanate, diphenylmethane
diisocyanate, octadecane diisocyanate, decane diisocyanate, and hexane diisocyanate.
The hydrocarbon may be a non-cyclic hydrocarbon or a cyclic hydrocarbon, or an aromatic
hydrocarbon, an alicyclic hydrocarbon, or an aliphatic hydrocarbon. Preferably, the
hydrocarbon is an aromatic hydrocarbon. The hydrocarbon has preferably 4 to 20 carbon
atoms, particularly 8 to 18 carbon atoms.
[0028] Monoamines are compounds in which one of the hydrogen atoms of the ammonia is substituted
with a hydrocarbon group. Preferred examples of the monoamines include octylamine,
dodecylamine, hexadecylamine, stearylamine, oleylamine, aniline, p-toluidine, and
cyclohexylamine. Diamines are compounds in which two of the hydrogen atoms of the
ammonia are substituted with hydrocarbon groups. Preferred examples of the diamines
include ethylenediamine, propanediamine, butanediamine, hexanediamine, octanediamine,
phenylenediamine, tolylenediamine, xylenediamine, and diaminodiphenylmethane. The
hydrocarbon groups of the monoamines and diamines may be non-cyclic hydrocarbon groups
or cyclic hydrocarbon groups, or aromatic hydrocarbon groups, alicyclic hydrocarbon
groups, or aliphatic hydrocarbon groups. Preferably, the monoamines and diamines contain
aliphatic hydrocarbon groups. The monoamines and diamines have preferably 2 to 20
carbon atoms, particularly preferably 4 to 18 carbon atoms.
Hydroxycarboxylic Acid Metal Salt
[0029] The present invention contains at least one of an α-hydroxycarboxylic acid metal
salt, and an ω-hydroxycarboxylic acid metal salt. It is preferable to contain both
an α-hydroxycarboxylic acid metal salt, and an ω-hydroxycarboxylic acid metal salt,
though only one of these may be contained. The metallic element forming the salt is
preferably an alkali metal or an alkali earth metal, particularly preferably calcium
or barium. The total content of the hydroxycarboxylic acid metal salts is 0.1 to 2
mass%, preferably 0.2 to 1 mass% with respect to the total amount of the grease composition.
The wear reducing effect will not be obtained when the total content of the hydroxycarboxylic
acid metal salts is less than 0.1 mass%, whereas the hydroxycarboxylic acid metal
salt may inhibit the effects of other components when the content is above 2 mass%.
[0030] In the present invention, the α- and ω-hydroxycarboxylic acids are preferably monovalent,
more preferably monovalent acids of 8 to 24 carbon atoms. The monovalent α-hydroxycarboxylic
acid is represented by R
1-CH(-OH)-COOH, and the ω-hydroxycarboxylic acid is represented by HO-CH
2-R
2-COOH. In the present invention, R
1 is preferably an alkyl group of 1 to 38 carbon atoms, or an alkenyl group of 2 to
38 carbon atoms, more preferably an alkyl group of 6 to 22 carbon atoms, or an alkenyl
group of 6 to 22 carbon atoms. R
2 is preferably an alkylene group of 1 to 38 carbon atoms, or an alkenylene group of
2 to 38 carbon atoms, more preferably an alkylene group of 6 to 22 carbon atoms, or
an alkenylene group of 6 to 22 carbon atoms.
[0031] Preferably, the present invention further contains metal salts of hydroxycarboxylic
acids other than α- and ω-hydroxycarboxylic acids, or metal salts of carboxylic acids
containing no hydroxyl group. Preferred examples of such carboxylic acid metal salts
include alkali metal salts or alkali earth metals, preferably calcium or barium salts
of α- and ω-hydroxycarboxylic acids in which the hydroxyl group is substituted at
different positions from the foregoing α- and ω-hydroxycarboxylic acids, or in which
two or more hydroxyl groups are substituted, and alkali metal salts or alkali earth
metals, preferably calcium or barium salts of carboxylic acids that do not have a
substitution of the hydroxyl group.
[0032] The hydroxycarboxylic acids, and the carboxylic acids may be obtained by chemical
synthesis. It is, however, preferable to use a lanolin fatty acid - an acid obtained
through purification (e.g., hydrolysis) of a wax-like substance adhering to sheep
hairs - as a raw material of these acids. When using a lanolin fatty acid as a raw
material, the α- and α-hydroxycarboxylic acids, and other preferred carboxylic acids
may be separately used. It is, however, preferable to prepare the lanolin fatty acid
directly into a metal salt, without separating these acids.
Amide Compound
[0033] The present invention further contains an amide compound. The amide compound, which
is a compound having at least one amide group (-NH-CO-), may be a compound containing
one amide group (monoamide), or a compound containing two amide groups (bisamide).
Preferably, saturated aliphatic monoamides, or saturated aliphatic bisamides are used.
[0034] The saturated aliphatic bisamides are most preferred for their advantages including
desirable heat resistance, and the ability to reduce the frictional resistance at
a sliding part even with a relatively small amount.
[0035] The saturated aliphatic monoamides are amide compounds of a saturated aliphatic monoamine
and a saturated aliphatic monocarboxylic acid. The saturated aliphatic bisamides may
be amide compounds of a saturated aliphatic diamine and a saturated aliphatic monocarboxylic
acid, or amide compounds of a saturated aliphatic dicarboxylic acid and a saturated
aliphatic monoamine.
[0036] A preferred saturated aliphatic amide compound has a melting point of 100 to 170°C,
and a molecular weight of 298 to 876.
[0037] The saturated aliphatic monoamides are represented by the following general formula
(1). The saturated aliphatic bisamides are represented by the following general formulae
(2) and (3).
R
11-CO-NH-R
12 ... (1)
R
13-CO-NH-A
1-NH-CO-R
14 ... (2)
R
15-NH-CO-A
2CO-NH-R
16 ... (3)
[0038] In the formulae, R
11, R
12, R
13, R
14, R
15, and R
16 each independently represent a saturated aliphatic hydrocarbon group of 5 to 25 carbon
atoms. In general formula (1), R
12 may be hydrogen. A
1 and A
2 represent divalent saturated aliphatic hydrocarbon groups of 1 to 10 carbon atoms,
and are preferably divalent saturated chain hydrocarbon groups of 1 to 4 carbon atoms.
[0039] Specifically, preferred examples of the saturated aliphatic monoamides include lauramide,
palmitamide, stearamide, and behenamide.
[0040] Preferred examples of the saturated aliphatic bisamides represented by formula (2)
include ethylene bis(stearamide), ethylene bis(isostearamide), ethylene bis(lauramide),
and methylene bis(lauramide). Preferred examples of the saturated aliphatic bisamides
represented by formula (3) include N,N'-bisstearylsebacamide.
[0041] The bisamides are preferably amide compounds in which R
13, R
14, R
15, and R
16 in formulae (2) and (3) are each independently a saturated chain hydrocarbon group
of 12 to 20 carbon atoms.
[0042] The amide compounds may be used alone or in a combination of two or more in any proportions.
The content of the amide compound is preferably 1 to 30 mass%, more preferably 5 to
20 mass% with respect to the total amount of the grease composition.
[0043] It is to be noted here that the amide compound, when thermofused in the presence
of the lubricant base oil, produces a state in which the lubricant base oil is held
in the amide compound forming a three-dimensional network structure. This further
lowers the coefficient of friction at a sliding part than when the amide compound
is simply dispersed or mixed in the grease.
Solid Lubricant Component
[0044] Preferably, the present invention further contains a solid lubricant component.
[0045] The solid lubricant component may be, for example, melamine cyanurate, molybdenum
disulfide, boron nitride, graphite, mica, fluororesin, fluorinated graphite, or a
molybdenum organic compound commonly used for lubricants. The content of the solid
lubricant component is preferably 0.1 to 10 mass%, more preferably 0.2 to 5 mass%
with respect to the total amount of the grease composition.
[0046] In the present invention, it is more preferable to use boron nitride or melamine
cyanurate as the solid lubricant component. Particularly preferably, a hexagonal,
atmospheric-phase boron nitride (h-BN) powder of a particle size suited for the intended
purpose may be appropriately selected and used. The solid lubricant component has
a particle diameter of preferably 1 to 10 µm.
Other Additives
[0047] Additives commonly used for lubricant oils and greases may be appropriately added,
as required, to the grease composition of the present invention, in addition to the
foregoing components. Examples of such additives include cleaners, dispersants, antiwear
agents, viscosity index improvers, antioxidants, extreme-pressure agents, anti-rusting
agents, and corrosion inhibitors.
Subject of Lubrication
[0048] The grease composition of the present invention is preferably used at sliding parts,
preferably for lubrication of various sliding members, for example, between metal
parts, metal and resin parts, and resin parts.
[0049] The sliding member resin may be a natural resin or a synthetic resin. Preferred as
synthetic resins are general-purpose plastics (e.g., polyethylene, polystyrene, polypropylene,
and polyvinyl chloride), and engineering plastics. Engineering plastics are particularly
preferred in terms of heat resistance, and mechanical strength. Examples of synthetic
resins include polyamide resins, polyacetal resins, polycarbonate resins, polysulfone
resins, polyphenylene sulfide resins, polyamideimide resins, polyetheretherketone
resins, phenolic resins, polyester resins, and epoxy resins. The grease composition
is particularly preferred for lubrication of polyamide resins, and polyoxymethylene
resins.
[0050] Examples of the applicable areas of the grease composition of the present invention
include transport machinery such as automobiles, railway, and aircraft; industrial
machines such as machine tools; home electrical appliances such as washing machines,
refrigerators, and vacuum cleaners; and precision machines such as watches and cameras.
The grease composition has use for, for example, bearings, gears, sliding surfaces,
belts, joints, and cams used for these machines. The grease composition is particularly
useful for improving the abrasion resistance of gears (e.g., spur wheels, helical
gears, crossed helical gears, hypoid gears, worm gears, and wheel gears) exposed to
a high-surface-pressure sliding environment.
Examples
[0051] The present invention is described below using Examples representing implementations
of the present invention. The present invention, however, is not limited to the following
implementations.
Preparation Method
[0052] Each component was put in a container in the amounts (mass%) shown in Tables 1 and
2, and heated to 150°C (a temperature equal to or greater than the melting point of
the amide compound). The mixture was then stirred with a magnetic stirrer, and cooled
to room temperature. The product was subjected to a dispersion process under applied
pressure using rollers (three rolls) to prepare a grease composition.
[0053] The components used are as follows.
- 1. Lubricant base oil:
- (1) Poly-α-olefin (Durasyn 170 available from INEOS)
Kinetic viscosity at 40°C: 68 mm2/s
Density at 15°C: 0.83 g/cm3
Viscosity index: 133
Pour point: -45°C
Flash point: 250°C
- (2) Polyolester (an ester of trimethylolpropane and an oleic acid of 18 carbon atoms)
Kinetic viscosity at 40°C: 46 mm2/s
Density at 15°C: 0.92 g/cm3
Viscosity index: 146
Pour point: -32.5°C
Flash point: 310°C
- 2. Thickening agent:
- (1) Urea-based thickening agent
Alicyclic diurea of cyclohexylamine and methylene diphenyl diisocyanate
- (2) Lithium-based thickening agent
A lithium salt of a mixed acid of 12-hydroxystearic acid and azelaic acid
- 3. Solid lubricant component:
- (1) Boron nitride
Hexagonal boron nitride having an average particle size of 2 µm as measured by laser
diffractometry (2) Melamine cyanurate (MCA)
Melamine cyanurate having an average particle size of 1 µm as measured by laser diffractometry
- 4. Amide compound:
- (1) Ethylene bis(stearamide) (guaranteed reagent)
- (2) Ethylene bis(lauramide) (guaranteed reagent)
- 5. Carboxylic acid metal salt
- (1) Barium lanolate
Content of α-hydroxycarboxylate: 30 mass%
Content of ω-hydroxycarboxylate: 5 mass%
Content of hydroxycarboxylates other than α- and ω-hydroxycarboxylates: 1 mass%
Content of carboxylate having no hydroxyl group: 40 mass%
Number of carbon atoms in hydroxycarboxylic acid: 8 to 24
Number of carbon atoms in carboxylic acid having no hydroxyl group: 8 to 24
- (2) Calcium lanolate
Content of α-hydroxycarboxylate: 30 mass%
Content of ω-hydroxycarboxylate: 5 mass%
Content of hydroxycarboxylates other than α- and ω-hydroxycarboxylates: 1 mass%
Content of carboxylate having no hydroxyl group: 40 mass%
Number of carbon atoms in hydroxycarboxylic acid: 8 to 24
Number of carbon atoms in carboxylic acid having no hydroxyl group: 8 to 24
Evaluation of Amount of Wear
[0054] Evaluation was made according to the ASTM D 3233 test method for measurement of load
bearing properties of lubricant oil, using a Falex friction tester. In this test,
a resin (polyamide resin (PA66)) pin was held between two steel (SUJ-2) V blocks,
and a sample was charged into a sample container. A 55-MPa load was applied with the
rotational axis held stationary, and the lubricant oil was tested for load bearing
properties at an oil temperature of 120°C under a rotation speed of 360 rpm. The amount
of wear was measured by measuring the reduction of the pin weight after 10 minutes.
The results are presented in Tables 1 and 2.
Evaluation Result
[0055] The amount of wear was considerably smaller in the grease compositions of Examples
that contained at least one of the α-hydroxycarboxylic acid metal salt and the ω-hydroxycarboxylic
acid metal salt with the thickening agent and the amide compound. On the other hand,
there was no large reduction in the amount of wear when the hydroxycarboxylic acid
metal salts were not contained, even when simple carboxylates, or a phosphite ester
(a known anti-wear agent) were added (Comparative Examples 1 to 7).
[Table 1]
| |
|
Example 1 |
Example 2 |
Example 3 |
Example 4 |
Comparative Example 1 |
Comparative Example 2 |
Comparative Example 3 |
Comparative Example 4 |
Comparative Example 5 |
Comparative Example 6 |
| Lubricant base oil |
Poly-α-olefin |
Balance |
Balance |
Balance |
Balance |
Balance |
Balance |
Balance |
Balance |
Balance |
Balance |
| Thickener |
Urea-based thickener |
10 |
10 |
10 |
10 |
10 |
10 |
10 |
10 |
10 |
10 |
| Amide compound |
Ethylene bis-stearylamide |
15 |
15 |
15 |
15 |
15 |
15 |
15 |
15 |
15 |
15 |
| Solid lubricants |
Boron nitride |
1.0 |
1.0 |
1.0 |
- |
1.0 |
1.0 |
1.0 |
1.0 |
1.0 |
1.0 |
| Carboxylic acid metal salt |
Barium lanolate |
1.0 |
2.0 |
- |
2.0 |
- |
- |
- |
- |
- |
- |
| Calcium lanolate |
- |
- |
1.0 |
- |
- |
- |
- |
- |
- |
- |
| Content of α-hydroxycarboxylic acid metal salt and ω-hydroxycarboxylic acid metal salt |
0.35 |
0.70 |
0.35 |
0.70 |
- |
- |
- |
- |
- |
- |
| Other additive compounds |
Oleylamide |
- |
- |
- |
- |
- |
1.0 |
- |
- |
- |
- |
| Aluminum stearate |
- |
- |
- |
- |
- |
- |
1.0 |
- |
- |
- |
| Zinc naphthenate |
- |
- |
- |
- |
- |
- |
- |
1.0 |
- |
- |
| naphtenate Phosphite ester |
- |
- |
- |
- |
- |
- |
- |
- |
1.0 |
- |
| Phosphate |
- |
- |
- |
- |
- |
- |
- |
- |
- |
1.0 |
| Evaluation results |
Worked penetration |
324 |
308 |
321 |
330 |
315 |
293 |
306 |
316 |
330 |
328 |
| Amount of wear (mg) |
0.5 |
0.6 |
0.8 |
0.8 |
1.3 |
0.9 |
1.0 |
1.0 |
0.9 |
1.2 |
[Table 2]
| |
|
Example 5 |
Example 6 |
Example 7 |
Example 8 |
Example 9 |
Example 10 |
Comparative Example 7 |
| Lubricant base oil |
Poly-α-olefin |
Balance |
Balance |
Balance |
Balance |
- |
Balance |
Balance |
| Polyolester |
- |
- |
- |
- |
Balance |
- |
- |
| Thickener |
Litium-based thickener |
10 |
10 |
10 |
10 |
10 |
10 |
10 |
| Amide compound |
Ethylene bis-stearylamide |
15 |
15 |
- |
15 |
15 |
15 |
- |
| Ethylene bis-laurylamide |
- |
- |
15 |
- |
- |
- |
- |
| Solid lubricants |
Boron nitride |
- |
2.0 |
2.0 |
- |
2.0 |
2.0 |
- |
| MCA |
- |
- |
- |
2.0 |
- |
- |
- |
| Carboxylic acid metal salt |
Barium lanolate |
1.0 |
1.0 |
1.0 |
1.0 |
1.0 |
- |
- |
| Calcium lanolate |
- |
- |
- |
- |
- |
1.0 |
- |
| Content of α-hydroxycarboxylic acid metal salt and ω-hydroxycarboxylic acid metal salt |
0.35 |
0.35 |
0.35 |
0.35 |
0.35 |
0.35 |
- |
| Evaluation results |
Worked penetration |
320 |
280 |
300 |
274 |
298 |
280 |
300 |
| Amount of wear (mg) |
1.2 |
0.8 |
1.0 |
1.0 |
1.0 |
1.0 |
1.6 |
Industrial Applicability
[0056] The grease composition of the present invention can greatly reduce an amount of wear
in sliding members, and is useful for lubrication of sliding parts of various members
of automobiles, electrical devices, and the like.