Technical Field
[0001] The present invention relates to a lubricating oil composition, a shock absorber
using the lubricating oil composition, and a method for using the lubricating oil
composition.
Background Art
[0002] A shock absorber is used by being filled with a lubricating oil composition for a
shock absorber, and is a mechanism mounted on a car body in order to generate a damping
force that damps the vibration of the car body, to optimize the friction characteristics
of the sliding portion to control the riding quality of the car body, to suppress
the friction wear of the sliding portion to secure durability, and the like.
[0003] Various lubricating oil compositions for a shock absorber that may be suitably used
in such a shock absorber have been developed.
[0004] For example, Patent Literature 1 discloses an invention relating to a lubricating
oil composition for a shock absorber that contains a lubricating base oil having a
predetermined kinematic viscosity, a nondispersed poly(meth)acrylate-based viscosity
modifier having a weight average molecular weight of 30,000 to 200,000, and a primary
zinc dialkyldithiophosphate and a secondary zinc dialkyldithiophosphate in a predetermined
content ratio.
Citation List
Patent Literature
Summary of Invention
Technical Problem
[0006] According to the studies by the present inventors, the lubricating oil composition
described in Patent Literature 1 has been found to be insufficient in an effect of
suppressing cavitation. In addition, a lubricating oil composition used for lubrication
of a shock absorber in which not only the effect of suppressing cavitation, but also
characteristics such as cold startability and shear stability are improved is required.
Solution to Problem
[0007] The present invention provides a lubricating oil composition used for lubrication
of a shock absorber containing a base oil, a polyalkyl (meth)acrylate having a predetermined
weight average molecular weight, and an olefin copolymer having a predetermined weight
average molecular weight. Specifically, the present invention provides the following
embodiments [1] to [10].
- [1] A lubricating oil composition used for lubrication of a shock absorber, comprising:
a base oil (A), a polyalkyl (meth)acrylate (B) having a weight average molecular weight
of 150,000 to 900,000, and an olefin copolymer (C) having a weight average molecular
weight of 100,000 or less.
- [2] The lubricating oil composition according to the above [1], wherein the total
content of the component (B) and the component (C) is 20.0 mass% or less based on
the total amount of the lubricating oil composition.
- [3] The lubricating oil composition according to the above [1] or [2], wherein a content
ratio [(B)/(C)] by mass of the component (B) to the component (C) is 1/99 to 90/10.
- [4] The lubricating oil composition according to any one of the above [1] to [3],
wherein a content of the component (B) is 0.1 to 10.0 mass% based on the total amount
of the lubricating oil composition.
- [5] The lubricating oil composition according to any one of the above [1] to [4],
wherein a content of the component (C) is 0.1 to 10.0 mass% based on the total amount
of the lubricating oil composition.
- [6] The lubricating oil composition according to any one of the above [1] to [5],
wherein a weight average molecular weight of the component (C) is 8,000 or more and
100,000 or less.
- [7] The lubricating oil composition according to any one of the above [1] to [6],
wherein the component (C) comprises an ethylene propylene copolymer (C1).
- [8] The lubricating oil composition according to any one of the above [1] to [7],
wherein the total content of the components (A) to (C) is 80 to 100 mass% based on
the total amount of the lubricating oil composition.
- [9] The lubricating oil composition according to any one of the above [1] to [8],
wherein a BF viscosity of the lubricating oil composition at -40°C is 1,500 mPa·s
or less.
- [10] Use of a lubricating oil composition, comprising applying the lubricating oil
composition according to any one of the above [1] to [9] to lubrication of a shock
absorber.
Advantageous Effects of Invention
[0008] The lubricating oil composition of one preferred embodiment of the present invention
is excellent in characteristics such as cold startability, shear stability, and an
effect of suppressing cavitation, and the lubricating oil composition of the particularly
preferred embodiment is excellent in all of the cold startability, the shear stability,
and the effect of suppressing cavitation, and therefore, it can be suitably applied
to lubrication of a shock absorber.
Brief Description of Drawing
[0009] [Figure 1] Figure 1 is a schematic diagram of a testing apparatus for evaluating
the effect of suppressing cavitation.
Description of Embodiments
[0010] In the present specification, a kinematic viscosity and a viscosity index mean values
measured and calculated in accordance with JIS K2283:2000.
[0011] In the present specification, the weight average molecular weight (Mw) and the number
average molecular weight (Mn) are values in terms of standard polystyrene measured
by gel permeation chromatography (GPC), and specifically mean values measured by the
method described in Examples.
[0012] In the numerical range described in the present specification, upper limit and lower
limit values can be arbitrarily combined. For example, when a description of "preferably
30 to 100, more preferably 40 to 80" is described as a numerical range, ranges such
as "30 to 80" and "40 to 100" are included in the numerical range described in the
present specification. For example, when a description of "preferably 30 or more,
more preferably 40 or more, and preferably 100 or less, more preferably 80 or less"
is described as a numerical range, ranges such as "30 to 80" and "40 to 100" are also
included in the numerical range described in the present specification.
[0013] In addition, for example, a description of "60 to 100" as the numerical range described
in the present specification means a range of "60 or more and 100 or less".
[Constitution of lubricating oil composition]
[0014] The lubricating oil composition of the present invention contains a base oil (A),
a polyalkyl (meth)acrylate (B) having a weight average molecular weight of 150,000
to 900,000, and an olefin copolymer (C) having a weight average molecular weight of
100,000 or less.
[0015] The lubricating oil composition used for a shock absorber requires various characteristics.
As one of such characteristics, the effect of suppressing cavitation is required.
Cavitation refers to a physical phenomenon in which generation and extinction of bubbles
occur in a short time due to the pressure difference in the flow of the lubricating
oil composition, leading to a factor for causing deterioration of responsiveness of
shock absorbers and noises. For example, the generation of cavitation in a shock absorber
mounted on a vehicle affects the ride quality of the vehicle and the like.
[0016] In addition, the lubricating oil composition used for a shock absorber requires not
only the effect of suppressing cavitation, but also characteristics such as cold startability
and shear stability.
[0017] The present inventors have intensively studied to obtain a lubricating oil composition
in which these characteristics are improved in good balance, and have found that a
combination of a polyalkyl (meth)acrylate (B) and an olefin copolymer (C) each having
a predetermined weight average molecular weight is useful.
[0018] That is, it has been found by the studies of the present inventors that the component
(B) is a factor that may improve the effect of suppressing cavitation and cold startability,
but causes a reduction of the shear stability, whereas the component (C) is a factor
that may improve the effect of suppressing cavitation and shear stability, but causes
a reduction of the cold startability.
[0019] Thus, the present inventors have found that a lubricating oil composition in which
cold startability, shear stability, and the effect of suppressing cavitation are improved
in good balance can be obtained by using the components (B) and (C) in combination.
The present invention has been made based on the findings.
[0020] In the lubricating oil composition of one embodiment of the present invention, from
the viewpoint of obtaining a lubricating oil composition in which cold startability,
shear stability, and the effect of suppressing cavitation are improved in good balance,
the content ratio [(B)/(C)] by mass of the component (B) to the component (C) is preferably
1/99 to 90/10, more preferably 5/85 to 80/20, more preferably 10/90 to 70/30, still
more preferably 15/85 to 60/40, still much more preferably 20/80 to 50/50, and particularly
preferably 25/75 to 45/55.
[0021] In the lubricating oil composition of one embodiment of the present invention, from
the viewpoint of obtaining a lubricating oil composition having a good balance between
cold startability and shear stability, the total content of the component (B) and
the component (C) is preferably 20.0 mass% or less, more preferably 16.0 mass% or
less, still more preferably 10.0 mass% or less, still much more preferably 8.0 mass%
or less, and particularly preferably 6.0 mass% or less, and from the viewpoint of
further improving the effect of suppressing cavitation, the total content of the component
(B) and the component (C) is preferably 0.2 mass% or more, more preferably 0.6 mass%
or more, still more preferably 1.0 mass% or more, still much more preferably 1.6 mass%
or more, and particularly preferably 2.0 mass% or more, based on the total amount
(100 mass%) of the lubricating oil composition.
[0022] Considering the handleability and the solubility with the component (A), the components
(B) and (C) are often commercially available in a form of a solution dissolved in
a diluent oil.
[0023] However, in the present specification, the content of the components (B) and (C)
is, in a solution diluted with a diluent oil, a content in terms of resin content
constituting the component (B) or (C), excluding the mass of the diluent oil.
[0024] The lubricating oil composition of one embodiment of the present invention may further
contain lubricating oil additives other than the components (B) to (C).
[0025] However, in the lubricating oil composition of one embodiment of the present invention,
from the viewpoint of obtaining a lubricating oil composition in which the effect
of suppressing cavitation and cold startability are further improved, the total content
of the components (A) to (C) is preferably 80 to 100 mass%, more preferably 85 to
100 mass%, still more preferably 90 to 100 mass%, still much more preferably 95 to
100 mass%, and particularly preferably 98 to 100 mass%, and further may be more than
98.5 mass% and 100 mass% or less, more than 99.0 mass% and 100 mass% or less, more
than 99.5 mass% and 100 mass% or less, or more than 99.7 mass% and 100 mass% or less,
based on the total amount (100 mass%) of the lubricating oil composition.
[0026] Hereinafter, details of each component contained in the lubricating oil composition
of one embodiment of the present invention will be described.
<Component (A): base oil>
[0027] As the base oil which is the component (A) used in one embodiment of the present
invention, one or more selected from mineral oils and synthetic oils can be mentioned.
[0028] Examples of the mineral oils include atmospheric residues obtained by subjecting
crude oils, such as paraffinic crude oil, intermediate base crude oil and naphthenic
crude oil, to atmospheric distillation; distillates obtained by subjecting these atmospheric
residues to vacuum distillation; and refined oils obtained by subjecting the distillates
to one or more of refining treatments, such as solvent deasphalting, solvent extraction,
hydrocracking, solvent dewaxing, catalytic dewaxing, and hydrorefining.
[0029] Examples of the synthetic oils include poly-α-olefins, such as an α-olefin homopolymer;
isoparaffin; polyalkylene glycol; ester oils, such as polyol ester, dibasic acid ester,
and phosphoric acid ester; ether oils, such as polyphenyl ether; alkylbenzene; alkylnaphthalene;
and synthetic oil (GTL) obtained by isomerizing wax (GTL WAX (Gas To Liquids WAX))
produced from natural gas through Fischer-Tropsch process or the like.
[0030] Among these, it is preferable to contain one or more selected from mineral oils classified
in Group II and Group III of API (American Petroleum Institute) base oil categories,
and synthetic oils, as the component (A) used in one embodiment of the present invention.
[0031] The kinematic viscosity of the component (A) used in one embodiment of the present
invention at 40°C is preferably 3.0 to 100 mm
2/s, more preferably 4.0 to 70 mm
2/s, still more preferably 5.0 to 40 mm
2/s, still much more preferably 5.5 to 30 mm
2/s, and particularly preferably 6.0 to 20 mm
2/s.
[0032] The viscosity index of the component (A) used in one embodiment of the present invention
is appropriately set depending on the applications of the lubricating oil composition,
and is preferably 70 or more, more preferably 80 or more, still more preferably 90
or more, still much more preferably 100 or more, and particularly preferably 105 or
more.
[0033] When a mixed oil that is a combination of two or more base oils is used as the component
(A) in one embodiment of the present invention, the kinematic viscosity and the viscosity
index of the mixed oil are preferably in the above ranges.
[0034] In the lubricating oil composition of one embodiment of the present invention, the
content of the component (A) is preferably 60 mass% or more, more preferably 70 mass%
or more, more preferably 75 mass% or more, still more preferably 80 mass% or more,
still much more preferably 85 mass% or more, and particularly preferably 90 mass%
or more, and is preferably 99.8 mass% or less, more preferably 99.5 mass% or less,
still more preferably 99.0 mass% or less, still much more preferably 98.5 mass% or
less, and particularly preferably 98.0 mass% or less, based on the total amount (100
mass%) of the lubricating oil composition.
<Component (B): polyalkyl (meth)acrylate>
[0035] The lubricating oil composition of the present invention contains a polyalkyl (meth)acrylate
having a weight average molecular weight (Mw) of 150,000 to 900,000 as the component
(B). When Mw is less than 150,000, the effect of suppressing cavitation is unlikely
to be exhibited. When Mw is more than 900,000, it tends to be difficult to achieve
both the effect of suppressing cavitation and shear stability. Since the component
(B) and the component (C) described below are used in combination, the lubricating
oil composition can be adjusted to have good shear stability.
[0036] The weight average molecular weight (Mw) of the polyalkyl (meth)acrylate used in
one embodiment of the present invention as the component (B) is 150,000 or more, and
from the viewpoint of obtaining a lubricating oil composition in which the effect
of suppressing cavitation and cold startability are further improved, it is preferably
200,000 or more, more preferably 250,000 or more, more preferably 260,000 or more,
more preferably 270,000 or more, more preferably 300,000 or more, still more preferably
320,000 or more, still more preferably 350,000 or more, still more preferably 370,000
or more, still more preferably 400,000 or more, still much more preferably 420,000
or more, still much more preferably 450,000 or more, still much more preferably 470,000
or more, still much more preferably 500,000 or more, and particularly preferably 520,000
or more. The weight average molecular weight (Mw) thereof is 900,000 or less, and
from the viewpoint of obtaining a lubricating oil composition having further improved
shear stability, it is preferably 850,000 or less, more preferably 800,000 or less,
more preferably 750,000 or less, still more preferably 700,000 or less, still much
more preferably 650,000 or less, and particularly preferably 600,000 or less.
[0037] In the lubricating oil composition of one embodiment of the present invention, from
the viewpoint of obtaining a lubricating oil composition in which the effect of suppressing
cavitation and cold startability are further improved, the content of the component
(B) is preferably 0.1 mass% or more, more preferably 0.2 mass% or more, still more
preferably 0.3 mass% or more, still much more preferably 0.5 mass% or more, and particularly
preferably 0.7 mass% or more, and from the viewpoint of obtaining a lubricating oil
composition having further improved shear stability, the content of the component
(B) is preferably 10.0 mass% or less, more preferably 8.0 mass% or less, still more
preferably 5.0 mass% or less, still much more preferably 3.0 mass% or less, and particularly
preferably 2.0 mass% or less, based on the total amount (100 mass%) of the lubricating
oil composition.
[0038] The component (B) used in one embodiment of the present invention may be a polymer
having a structural unit derived from an alkyl acrylate or an alkyl methacrylate (hereinafter,
collectively referred to as "alkyl (meth)acrylate"), or may be a copolymer having
a structural unit derived from a monomer other than the alkyl (meth)acrylate.
[0039] The number of carbon atoms of the alkyl group in the alkyl (meth)acrylate may be
1 or more, 3 or more, 5 or more, or 10 or more, and may be 60 or less, 40 or less,
30 or less, or 20 or less.
[0040] In the component (B) used in one embodiment of the present invention, the content
of the structural unit derived from the alkyl (meth)acrylate may be 10 mol% or more,
30 mol% or more, 50 mol% or more, 60 mol% or more, 70 mol% or more, 80 mol% or more,
90 mol% or more, 95 mol% or more, or 99 mol% or more, based on the total amount (100
mol%) of the structural unit of the component (B) .
<<Comb-shaped polymer>>
[0041] The component (B) used in one embodiment of the present invention may be a comb-shaped
polymer.
[0042] The comb-shaped polymer used in one embodiment of the present invention as the component
(B) is only required to be a polymer having a structure including a large number of
three-way branch points from which a side chain having a high-molecular weight comes
out, in the main chain.
[0043] SSI (shear stability index) of the comb-shaped polymer used in one embodiment of
the present invention as the component (B) is preferably 100 or less, more preferably
80 or less, still more preferably 70 or less, still much more preferably 60 or less,
and particularly preferably 50 or less.
[0044] The lower limit value of SSI of the comb-shaped polymer is not particularly limited,
and is usually 0.1 or more.
[0045] In the present specification, SSI (shear stability index) represents a decrease in
viscosity caused by shear derived from the polymer component by percentage, and is
a value measured in accordance with JPI-5S-29-06, more specifically, a value calculated
by the following expression (1).

[0046] In the above expression (1), Kv
0 is a value of the kinematic viscosity of a sample oil at 100°C in which the polymer
component is diluted in a mineral oil, and Kv
1 is a value of the kinematic viscosity of the sample oil at 100°C in which the polymer
component is diluted in a mineral oil, after being subjected to irradiation with ultrasonic
wave for 30 minutes by an output method in accordance with the procedures of JPI-5S-29-06.
Moreover, Kv
oil is a value of the kinematic viscosity of the mineral oil at 100°C used when the polymer
component is diluted.
[0047] The value of SSI of the comb-shaped polymer varies with the structure thereof. Specifically,
there are the following tendencies, and by considering these matters, the value of
SSI of the comb-shaped polymer can be easily adjusted. The following matters are merely
examples, and the value of SSI of the comb-shaped polymer can also be adjusted by
considering matters other than these matters.
- A comb-shaped polymer whose side chain is constituted of the macromonomer (x1) and
in which the content of the structural unit (x1) derived from the macromonomer (x1)
is 0.5 mol% or more, based on the total amount (100 mol%) of the structural unit tends
to have a low value of SSI.
- As the molecular weight of the macromonomer (x1) constituting the side chain of the
comb-shaped polymer becomes higher, the value of SSI tends to become lower.
[0048] The comb-shaped polymer used in one embodiment of the present invention as the component
(B) is preferably a polymer at least having a structural unit (x1) derived from a
macromonomer (x1). This structural unit (x1) corresponds to the aforementioned "side
chain having a high-molecular weight".
[0049] In the present specification, the above "macromonomer (x1)" means a high-molecular
weight monomer having a polymerizable functional group, and is preferably a high-molecular
weight monomer having a polymerizable functional group at a terminal thereof.
[0050] In the comb-shaped polymer used in one embodiment of the present invention as the
component (B), the content of the structural unit (X1) is preferably 0.5 to 20 mol%,
more preferably 0.7 to 10 mol%, and still more preferably 0.9 to 5 mol%, based on
the total amount (100 mol%) of the structural unit of the comb-shaped polymer.
[0051] In the present specification, the content of the structural unit in the comb-shaped
polymer means a value calculated by analyzing the
13C-NMR quantitative spectrum.
[0052] The number average molecular weight (Mn) of the macromonomer (x1) is preferably 300
or more, more preferably 400 or more, still more preferably 500 or more, and preferably
100,000 or less, more preferably 50,000 or less, still more preferably 20,000 or less.
[0053] That is to say, the number average molecular weight (Mn) of the macromonomer (x1)
is preferably 300 to 100,000, more preferably 400 to 50,000, and still more preferably
500 to 20,000.
[0054] Examples of the polymerizable functional group included in the macromonomer (x1)
include an acryloyl group (CH
2=CH-COO-), a methacryloyl group (CH
2=CCH
3-COO-), an ethenyl group (CH
2=CH-), a vinyl ether group (CH
2=CHO-), an allyl group (CH
2=CH-CH
2-), an allyl ether group (CH
2=CH-CH
2-O-), a group represented by CH
2=CH-CONH-, and a group represented by CH
2=CCH
3-CONH-.
[0055] In addition to the above polymerizable functional group, the macromonomer (x1) may
have, for example, one or more repeating units represented by the following general
formulae (i) to (iii).

[0056] In the above general formula (i), R
b1 is a linear or branched alkylene group having 1 to 10 carbon atoms.
[0057] In the general formula (ii), R
b2 is a linear or branched alkylene group having 2 to 4 carbon atoms.
[0058] In the general formula (iii), R
b3 is a hydrogen atom or a methyl group. R
b4 is a linear or branched alkyl group having 1 to 10 carbon atoms.
[0059] When the macromonomer (x1) has a plurality of repeating units represented by each
of the above general formulae (i) to (iii), R
b1, R
b2, R
b3 and R
b4 may be each the same as one another or may be different from one another.
[0060] In one embodiment of the present invention, the macromonomer (x1) is preferably a
polymer having a repeating unit represented by the general formula (i), and more preferably
a polymer having a repeating unit (X1-1) in which R
b1 in the general formula (i) is at least one selected from a 1,2-butylene group and
a 1,4-butylene group.
[0061] The content of the repeating unit (X1-1) is preferably 1 to 100 mol%, more preferably
20 to 95 mol%, still more preferably 40 to 90 mol%, and still much more preferably
50 to 80 mol%, based on the total amount (100 mol%) of the structural unit of the
macromonomer (x1).
[0062] When the macromonomer (x1) is a copolymer having two or more repeating units selected
from the general formulae (i) to (iii), the form of copolymer may be a block copolymer
or may be a random copolymer.
[0063] The comb-shaped polymer used in one embodiment of the present invention as a component
(B) may be a homopolymer consisting only of a structural unit (x1) derived from one
macromonomer (x1), or may be a copolymer having a structural unit (x1) derived from
two or more macromonomers (x1).
[0064] The comb-shaped polymer used in one embodiment of the present invention as a component
(B) may be a copolymer having a structural unit (X2) derived from a monomer other
than the macromonomer (x1) together with a structural unit (x1) derived from a macromonomer
(x1).
[0065] As a specific structure of such a comb-shaped polymer, a copolymer having a side
chain including the structural unit (x1) derived from the macromonomer (x1) relative
to the main chain including the structural unit (X2) derived from the monomer (x2)
is preferable.
[0066] Examples of the monomer (x2) include alkyl (meth)acrylate, a nitrogen atom-containing
vinyl monomer, a hydroxyl group-containing vinyl monomer, a phosphorus atom-containing
monomer, an aliphatic hydrocarbon-based vinyl monomer, a cycloaliphatic hydrocarbon-based
vinyl monomer, vinyl ester, vinyl ether, vinyl ketone, an epoxy group-containing vinyl
monomer, a halogen elementcontaining vinyl monomer, an ester of unsaturated polycarboxylic
acid, (di)alkyl fumarate, (di)alkyl maleate, and an aromatic hydrocarbon-based vinyl
monomer.
[0067] The monomer (x2) is preferably a monomer other than the phosphorus atom-containing
monomer and the aromatic hydrocarbon-based vinyl monomer, more preferably includes
one or more selected from a monomer represented by the following general formula (a1),
alkyl(meth)acrylate, and a hydroxyl group-containing vinyl monomer, and still more
preferably includes at least a hydroxyl group-containing vinyl monomer (x2-d).

[0068] In the general formula (a1), R
b11 is a hydrogen atom or a methyl group.
[0069] R
b12 is a single bond, a linear or branched alkylene group having 1 to 10 carbon atoms,
-O-, or -NH-.
[0070] R
b13 is a linear or branched alkylene group having 2 to 4 carbon atoms. Moreover, n represents
an integer of 1 or more (preferably an integer of 1 to 20, and more preferably an
integer of 1 to 5). When n is an integer of 2 or more, each R
b13 may be the same as one another or may be different from one another, and further,
the (R
b13O)
n moiety may be a random bond or a block bond.
[0071] R
b14 is a linear or branched alkyl group having 1 to 60 (preferably 10 to 50, and more
preferably 20 to 40) carbon atoms.
<Olefin copolymer (C)>
[0072] The lubricating oil composition of the present invention contains an olefin copolymer
having a weight average molecular weight (Mw) of 100,000 or less as the component
(C). By using the olefin copolymer having Mw within the above range and the component
(B) in combination, a lubricating oil composition in which the effect of suppressing
cavitation and shear stability are improved can be obtained. Since the component (C)
and the component (B) described above are used in combination, the lubricating oil
composition can be adjusted to have good cold startability.
[0073] The weight average molecular weight (Mw) of the olefin copolymer used in one embodiment
of the present invention as the component (C) is 100,000 or less, and from the viewpoint
of obtaining a lubricating oil composition having further improved cold startability
and shear stability while having a further improved effect of suppressing cavitation,
it is preferably 80,000 or less, more preferably 70,000 or less, more preferably 60,000
or less, still more preferably 40,000 or less, still much more preferably 30,000 or
less, and particularly preferably 25,000 or less.
[0074] The weight average molecular weight (Mw) of the olefin copolymer as the component
(C) may be 500 or more, 1,000 or more, 3,000 or more, 5,000 or more, 7,000 or more,
8,000 or more, more than 8,000, 8,500 or more, 9,000 or more, 9,500 or more, 10,000
or more, 11,000 or more, 12,000 or more, or 13,000 or more.
[0075] In the lubricating oil composition of one embodiment of the present invention, from
the viewpoint of obtaining a lubricating oil composition in which the effect of suppressing
cavitation and shear stability are further improved, the content of the component
(C) is preferably 0.1 mass% or more, more preferably 0.3 mass% or more, still more
preferably 0.5 mass% or more, still much more preferably 0.8 mass% or more, and particularly
preferably 1.0 mass% or more, and from the viewpoint of obtaining a lubricating oil
composition having further improved cold startability, the content of the component
(C) is preferably 10.0 mass% or less, more preferably 8.0 mass% or less, still more
preferably 5.0 mass% or less, still much more preferably 4.0 mass% or less, and particularly
preferably 3.0 mass% or less, and further may be 2.5 mass% or less, or 2.0 mass% or
less, based on the total amount (100 mass%) of the lubricating oil composition.
[0076] The component (C) used in one embodiment of the present invention is preferably a
copolymer having a structural unit derived from a monomer having an alkenyl group,
and examples thereof include a copolymer of an
α-olefin having 2 to 20 (preferably 2 to 16, more preferably 2 to 14) carbon atoms,
and more specific examples thereof include an ethylene-
α-olefin copolymer.
[0077] The number of carbon atoms of the
α-olefin constituting the ethylene-
α-olefin copolymer is preferably 3 to 20, more preferably 3 to 16, still more preferably
3 to 14, still much more preferably 3 to 6, and particularly preferably 3.
[0078] The component (C) used in one embodiment of the present invention may be a dispersion
type olefin-based copolymer.
[0079] Examples of the dispersion type olefin-based copolymer include a copolymer obtained
by graftpolymerizing the aforementioned ethylene-
α-olefin copolymer with maleic acid, N-vinyl pyrrolidone, N-vinyl imidazole, or glycidyl
acrylate.
[0080] The component (C) used in one embodiment of the present invention may be a copolymer
further having a structural unit derived from an aromatic monomer together with a
structural unit derived from a monomer having an alkenyl group. Examples of such an
olefin-based copolymer include styrene-based copolymers such as a styrene-diene copolymer
and a styrene-isoprene copolymer.
[0081] Among these, from the viewpoint of obtaining a lubricating oil composition in which
the effect of suppressing cavitation and shear stability are improved, the component
(C) used in one embodiment of the present invention preferably contains an ethylene
propylene copolymer (C1).
[0082] In the lubricating oil composition of one embodiment of the present invention, the
content ratio of the component (C1) is preferably 30 to 100 mass%, more preferably
50 to 100 mass%, still more preferably 70 to 100 mass%, still much more preferably
80 to 100 mass%, and particularly preferably 90 to 100 mass%, based on the total amount
(100 mass%) of the component (C) contained in the lubricating oil composition.
<Lubricating oil additives>
[0083] The lubricating oil composition of one embodiment of the present invention may further
contain lubricating oil additives other than the component (B) and the component (C)
when needed as long as the effects of the present invention are not impaired.
[0084] Examples of such lubricating oil additives include an antioxidant such as a phenol-based
antioxidant and an amino-based antioxidant; a metal-based detergent such as metal
sulfonate, metal salicylate, and metal phenate; ashless dispersants such as alkenyl
succinimide; a friction modifier such as a molybdenum-based friction modifier, a fatty
acid ester, fatty acid, and an aliphatic alcohol; an anti-wear agent such as zinc
dithiophosphate; an extreme-pressure agent such as a phosphorus-based extreme-pressure
agent, a sulfur-based extreme-pressure agent, and a sulfur-phosphorus-based extreme-pressure
agent; an anti-foaming agent such as a silicone-based anti-foaming agent; a metal
deactivator such as a benzotriazole-based compound; an anticorrosive; and an antistatic
agent.
[0085] These lubricating oil additives may be each used singly, or may be each used in combination
of two or more.
[0086] The contents of these lubricating oil additives can be each appropriately prepared
as long as the effects of the present invention are not impaired, but the contents
of the additives are each independently usually 0.001 to 15 mass%, preferably 0.005
to 10 mass%, and more preferably 0.01 to 5 mass%, based on the total amount (100 mass%)
of the lubricating oil composition.
<Production method for lubricating oil composition>
[0087] The production method for the lubricating oil composition of one embodiment of the
present invention is not particularly limited, but from the viewpoint of productivity,
preferable is a method having a step of compounding the component (B) and the component
(C), and if necessary, other lubricating oil additives with the component (A).
[0088] From the viewpoint of compatibility with the component (A), the resin component such
as the component (B) and the component (C) is preferably in a form of a solution dissolved
in a diluent oil and the solution is preferably compounded with the component (A).
[Properties of lubricating oil composition]
[0089] The kinematic viscosity of the lubricating oil composition of one embodiment of the
present invention at 40°C is preferably 5.0 to 130 mm
2/s, more preferably 6.5 to 100 mm
2/s, still more preferably 8.0 to 100 mm
2/s, still much more preferably 10.0 to 60 mm
2/s, and particularly preferably 11.0 to 40 mm
2/s.
[0090] The kinematic viscosity of the lubricating oil composition of one embodiment of the
present invention at 100°C is preferably 2.0 to 30 mm
2/s, more preferably 2.3 to 20 mm
2/s, still more preferably 2.6 to 15 mm
2/s, still much more preferably 3.0 to 10 mm
2/s, and particularly preferably 3.2 to 7.0 mm
2/s.
[0091] The kinematic viscosity of the lubricating oil composition of one embodiment of the
present invention at 150°C is preferably 1.0 to 20 mm
2/s, more preferably 1.2 to 10 mm
2/s, still more preferably 1.4 to 7.0 mm
2/s, still much more preferably 1.6 to 5.0 mm
2/s, and particularly preferably 1.8 to 3.0 mm
2/s.
[0092] The viscosity index of the lubricating oil composition of one embodiment of the present
invention is preferably 100 or more, more preferably 120 or more, still more preferably
140 or more, still much more preferably 160 or more, and particularly preferably 180
or more.
[0093] From the viewpoint of obtaining a lubricating oil composition having good cold startability,
the BF viscosity (Brookfield viscosity) of the lubricating oil composition of one
embodiment of the present invention at -40°C is preferably 1,500 mPa·s or less, more
preferably 1,400 mPa·s or less, still more preferably 1,300 mPa·s or less, and still
much more preferably 1,200 mPa·s or less, and is preferably 100 mPa·s or more, more
preferably 300 mPa·s or more, still more preferably 500 mPa-s or more, and still much
more preferably 700 mPa·s or more.
[0094] In the present specification, the BF viscosity means a value measured in accordance
with ASTM D2983-09.
[0095] From the viewpoint of obtaining a lubricating oil composition having good shear stability,
the kinematic viscosity reduction rate calculated in accordance with the method described
in Examples of the lubricating oil composition of one embodiment of the present invention
below is preferably less than 11.0%, more preferably less than 10.5%, still more preferably
less than 10.0%, and still much more preferably less than 9.5%.
[0096] From the viewpoint of obtaining a lubricating oil composition excellent in the effect
of suppressing cavitation, the value of the cavitation factor calculated in accordance
with the method described in Examples of the lubricating oil composition of one embodiment
of the present invention below is preferably 0.45 or less, more preferably 0.44 or
less, and still more preferably 0.43 or less, and typically 0.40 or more.
[Characteristics and use application of lubricating oil composition]
[0097] The lubricating oil composition of one embodiment of the present invention has excellent
characteristics such as cold startability, shear stability, and the effect of suppressing
cavitation.
[0098] Thus, the lubricating oil composition of one embodiment of the present invention
can be suitably used for lubrication of a shock absorber, and more specifically, can
be used for both a double cylinder type shock absorber and a single cylinder type
shock absorber, and can be suitably used for both a shock absorber for two wheels
and a shock absorber for four wheels.
[0099] When these characteristics of the lubricating oil composition of one embodiment of
the present invention are taken into consideration, the present invention can also
provide the following [1] and [2].
- [1] A shock absorber filled with the aforementioned lubricating oil composition of
one embodiment of the present invention.
- [2] Use of a lubricating oil composition, wherein the aforementioned lubricating oil
composition of one embodiment of the present invention is applied to lubrication of
a shock absorber.
Examples
[0100] Next, the present invention will be described in much more detail with reference
to Examples, but the present invention is in no way limited to these Examples. Measuring
methods for various properties are as follows.
(1) Kinematic viscosity, viscosity index
[0101] The kinematic viscosity and viscosity index were measured and calculated in accordance
with JIS K2283:2000.
(2) Weight average molecular weight (Mw)
[0102] Using a gel permeation chromatograph apparatus (manufactured by Agilent Technologies,
Inc., "1260 model HPLC"), the weight-average molecular weight was measured under the
following conditions, and a value measured in terms of standard polystyrene was used.
(Measurement conditions)
[0103]
Column: sequentially connected two of "Shodex LF404".
Column temperature: 35°C
Developing solvent: chloroform
Flow rate: 0.3 mL/min
Example 1 and Comparative Examples 1 to 8
[0104] Each additive was compounded with the base oil in the types and compounding amounts
shown in Table 1, thereby preparing each lubricating oil composition. The compounding
amount of each additive described in Table 1 describes the compounding amount in terms
of active ingredients (in terms of solid content) from which the mass of the diluent
oil was excluded, even when each additive was compounded in a state being dissolved
in the diluent oil.
[0105] Details of the base oil and each additive used in the preparation of each lubricating
oil composition are as follows.
<Base oil>
[0106] "Paraffinic mineral oil": paraffinic mineral oil, 40°C kinematic viscosity = 7.1
mm
2/s, 100°C kinematic viscosity = 2.17 mm
2/s, viscosity index = 109, 15°C density = 0.82 g/cm
3.
<PMA>
[0107] "PMA (550,000)": polyalkyl (meth)acrylate, weight average molecular weight (Mw) =
550,000.
[0108] "PMA (29,000)": polyalkyl (meth)acrylate, weight average molecular weight (Mw) =
29,000.
[0109] "PMA (140,000)": polyalkyl (meth)acrylate, weight average molecular weight (Mw) =
140,000.
<OCP>
[0110] "OCP (17,000)": ethylene propylene copolymer, weight average molecular weight (Mw)
= 17,000.
[0111] "OCP (780,000)": olefin copolymer, weight average molecular weight (Mw) = 780,000.
[0112] Regarding the lubricating oil composition prepared, the 40°C kinematic viscosity,
100°C kinematic viscosity, 150°C kinematic viscosity, and viscosity index were measured
or calculated in accordance with the aforementioned method, and the following measurement
or evaluation was carried out. The results of them are set forth in Table 1.
(1) Evaluation of cold startability
[0113] The BF viscosity at -40°C was measured in accordance with ASTM D2983-09.
[0114] It is deemed that as the BF viscosity becomes lower, the lubricating oil composition
has more excellent cold startability. When the BF viscosity at -40°C was 1,500 mPa·s
or less, the lubricating oil composition was determined to have excellent cold startability.
(2) Evaluation of shear stability
[0115] The shear test was carried out in accordance with the ultrasonic A method (JPI-5S-29)
by using the lubricating oil composition prepared as the sample oil and irradiating
30 mL of the sample oil with ultrasonic waves at 25°C for 60 minutes. As the output
voltage of ultrasonic waves, the value of an output voltage at which the reduction
rate of the 40°C kinematic viscosity after 30 mL of a standard oil whose 40°C kinematic
viscosity was measured in advance was irradiated with ultrasonic waves at 25°C for
60 minutes was 25% was employed.
[0116] Then, the 40°C kinematic viscosity of the sample oil was measured before and after
the shear test, and the kinematic viscosity reduction rate was calculated by the following
expression, thereby evaluating the shear stability.

[0117] It is deemed that as the value of the kinematic viscosity reduction rate becomes
smaller, the lubricating oil composition has more excellent shear stability. When
the value of the kinematic viscosity reduction rate was less than 11.0%, the lubricating
oil composition was determined to have excellent shear stability.
(3) Evaluation of effect of suppressing cavitation
[0118] Figure 1 is a schematic diagram of a testing apparatus for evaluating the effect
of suppressing cavitation. A testing apparatus 1 shown in Figure 1 has an oil tank
11 that stores the sample oil of the subject to be evaluated, a pump 12 that circulates
the sample oil, a heater 13 that adjusts the temperature of the sample oil, a flowmeter
14 that controls the flow velocity of the sample oil, valves 15a, 15b, and 15c that
control the flow of the sample oil, an observation tank 16 provided with an observation
window made of sapphire on a side surface and an orifice 16a with a diameter of 1
mm in an inlet on the upstream side, pressure gauges 17a and 17b on the upstream side
and the downstream side of the observation tank, and a thermocouple 18.
[0119] First, the oil tank 11 was filled with the lubricating oil composition prepared as
the sample oil, the valves 15a, 15b, and 15c were fully opened, the pump 12 and the
heater 13 were operated, and the observation tank 16 was also filled with the sample
oil while allowing the sample oil to be circulated along with a flow path 1 and a
flow path 2. Then, the state where the temperature of the sample oil reached 150°C
and stabilized was taken as the initial state.
[0120] From the initial state, while limiting the flow of the sample oil along with the
flow path 2 by gradually closing the valve 15c from the fully-opened state, the state
where the pressure gauge 17a on the upstream side exhibited "0.5 MPa" was taken as
the starting point, and the valve 15a on the upstream side and the valve 15b on the
downstream side were controlled to pressurize the sample oil in a stepwise manner
until the pressure gauge 17a on the upstream side exhibited "5.0 MPa". In the pressurizing
process, the degree of generation of cavitation was visually observed through a transparent
window of the observation tank 16, based on the cavitation score whose criteria were
defined in advance depending on the degree of generation of cavitation. At a point
where the cavitation score becomes "5", the pressure on the upstream side Pu shown
by the pressure gauge 17a on the upstream side and the pressure on the downstream
side Pd shown by the pressure gauge 17b on the downstream side were confirmed, thereby
calculating the cavitation factor.
[0121] The above cavitation score was evaluated by 11-grade in increments of one, by taking
no generation of cavitation as "0" and the state where cavitation was most generated
was "10". The criteria at each grade were based on the criteria defined in advance
depending on the degree of generation of cavitation.
[0122] The cavitation factor was calculated from the following expression, and the value
was set forth in Table 1.

[0123] In the above expression, Pu is the pressure on the upstream side (unit: Pa) and Pd
is the pressure on the downstream side (unit: Pa).
[0124] It is deemed that as the cavitation factor calculated from the above expression becomes
smaller, the lubricating oil composition has a higher effect of suppressing cavitation.
When the value of the cavitation factor was 0.45 or less, the lubricating oil composition
was determined to have an excellent effect of suppressing cavitation.
[0125] When cavitation with a cavitation score of "5" or more was already generated at the
starting point at which the pressure on the upstream side exhibits 0.5 MPa, cavitation
was considered to be generated at all times, which is set forth in Table 1 as "F".
[Table 1]
[0126]
Table 1
|
Example 1 |
Comparative Example 1 |
Comparative Example 2 |
Comparative Example 3 |
Comparative Example 4 |
Comparative Example 5 |
Comparative Example 6 |
Comparative Example 7 |
Comparative Example 8 |
Compositi on |
Base oil |
Paraffinic mineral oil |
mass% |
97.23 |
100.00 |
96.00 |
98.46 |
91.74 |
95.10 |
97.60 |
96.25 |
95.00 |
PMA |
PMA (550,000) |
mass% |
0.77 |
- |
- |
1.54 |
- |
0.77 |
- |
- |
- |
PMA (29,000) |
mass% |
- |
- |
- |
- |
8.26 |
4.13 |
- |
- |
- |
PMA (140,000) |
mass% |
- |
- |
- |
- |
- |
- |
2.40 |
- |
- |
OCP |
OCP (17,000) |
mass% |
2.00 |
- |
4.00 |
- |
- |
- |
- |
- |
- |
OCP (780,000) |
mass% |
- |
- |
- |
- |
- |
- |
- |
3.75 |
5.00 |
Total |
mass% |
100.0 |
100.0 |
100.0 |
100.0 |
100.0 |
100.0 |
100.0 |
100.0 |
100.0 |
Properties |
40°C kinematic viscosity |
mm2/s |
12.28 |
7.12 |
13.23 |
10.47 |
12.50 |
11.76 |
10.74 |
13.25 |
14.19 |
100°C kinematic viscosity |
mm2/s |
3.658 |
2.174 |
3.554 |
3.551 |
3.836 |
3.796 |
3.437 |
3.771 |
3.817 |
150°C kinematic viscosity |
mm2/s |
1.988 |
1.224 |
1.867 |
2.026 |
2.103 |
2.121 |
1.922 |
2.014 |
1.998 |
Viscosity index |
- |
206 |
109 |
159 |
264 |
228 |
250 |
227 |
192 |
173 |
Evaluation |
(1) Low temperature fluidity |
BF viscosity (-40°C) |
mPa·s |
1180 |
(*1) |
(*1) |
850 |
1420 |
1020 |
820 |
1610 |
(*1) |
(2) Shear stability |
Kinematic viscosity reduction rate |
% |
9.4 |
0.0 |
0.3 |
19.6 |
0.1 |
11.7 |
11.0 |
22.1 |
22.0 |
(3) Effect of suppressing cavitation |
Cavitation factor |
- |
0.43 |
F |
0.30 |
0.33 |
0.48 |
0.49 |
F |
0.34 |
F |
(*1) Solidified and unmeasurable |
[0127] As shown in Table 1, the lubricating oil composition prepared in Example 1 has excellent
cold startability and shear stability, resulting in a high effect of suppressing cavitation.
On the other hand, the lubricating oil compositions prepared in Comparative Examples
1 to 8 resulted in having poor cold startability, poor shear stability, or a poor
effect of suppressing cavitation.
Reference Signs List
[0128]
- 1
- Testing apparatus
- 11
- Oil tank
- 12
- Pump
- 13
- Heater
- 14
- Flowmeter
- 15a, 15b, 15c
- Valve
- 16
- Observation tank
- 16a
- Orifice
- 17a, 17b
- Pressure gauge
- 18
- Thermocouple