Technical Field
[0001] The present invention relates to lubricating oil compositions with excellent insulation
properties and lubricity.
Background Art
[0002] A variety of electronic control devices have been used in the mechanisms of an automobile.
Some of them may be used in lubricating oil and thus the insulation properties thereof
have become important. In particular, lubricating oils for the transmission, both
the transmission and electric motor, or the device in which a lubricating system is
shared by the transmission and electric motor, mounted in a fuel cell electric vehicle,
an electric vehicle or a hybrid vehicle have been required to have higher insulation
properties because these devices operate using a high electric voltage. Furthermore,
in recent years, the transmission has been required to be improved in power transmission
efficiency and down-sized as well as weight-reduced so as to improve fuel efficiency
and thus has been applied with a higher load. The lubricating oil has, therefore,
been demanded to have insulation properties as well as more improved anti-wear properties
and anti-seizure properties.
[0003] In addition to the above-described properties, the lubricating oil for transmissions
are required to have friction characteristics conforming with the characteristics
of a clutch, viscosity characteristics ranging from low temperatures to high temperatures
so that an appropriate hydraulic pressure control can be achieved, i.e., viscosity
retention which is not affected on temperature as much as possible, and oxidation
stability and detergent dispersibility to keep the device clean so that the control
device thereof can operate appropriately. Furthermore, these characteristics are generally
needed to be retained during the working life of the device. For this purpose, a variety
of additives are used in a transmission lubricating oil.
[0004] So far, as such transmission lubricating oils, some oils have been proposed such
as an automobile transmission oil composition comprising a base oil selected from
mineral oils, synthetic oils and mixtures thereof and a phosphorus compound selected
from hydrocarbon group-containing zinc dithiophosphate, triaryl phosphate, triaryl
thiophosphate and a mixture thereof in an amount of 0.1 to 15.0 percent by mass on
the total mass composition basis and having a 80°C volume resistivity of 1×10
7 Ω·m or greater (Patent Literature 1) and a transmission oil composition comprising
a base oil selected from mineral oils, poly-α-olefins and hydrogenated compounds thereof,
alkylbenzenes, ester-based compounds and mixtures thereof and having a 80°C kinematic
viscosity of 1.5 to 4.0 mm
2/s, a phosphorus compound selected from hydrocarbon group-containing zinc dithiophosphate,
triaryl thiophosphates and mixtures thereof in an amount of 0.1 to 4.0 percent by
mass on the total composition mass basis, and an ashless dispersant and having a 80°C
volume resistivity of 1×10
8 Ω·m or greater (Patent Literature 2).
Citation List
Patent Literature
Summary of Invention
Technical Problem
[0006] As described above, a variety of additives are used in a transmission oil but would
alone or in combination degrade the insulation properties, anti-wear properties or
anti-seizure properties. The present invention aims at providing a lubricating oil
composition maintaining properties necessary for a transmission and having more excellent
insulation properties and anti-wear properties and more improved anti-seizure properties
than the prior art.
Solution to Problem
[0007] That is, the present invention relates to a lubricating oil composition comprising:
(A) a lubricating oil base oil; (B) at least one type of phosphorus compound selected
from the group consisting of phosphorus compounds having at least one hydroxyl group
and/or at least one thiol group; and (C) an ashless dispersant having a functional
group containing as a dispersion group in an amount of less than 0.001 percent by
mass on the basis of nitrogen on the total composition mass basis or no such an ashless
dispersant at all, the composition having a 80°C volume resistivity of 5×10
8 Ω·m or greater.
[0008] The present invention also relates to the above-described lubricating oil composition
wherein (B) the phosphorus compound having a hydrocarbon group having 16 or fewer
carbon atoms.
[0009] The present invention also relates to the above-described lubricating oil composition
used for the transmission, both transmission and electric motor, or the device in
which a lubricating system is shared by the transmission and electric motor, mounted
in a fuel cell electric vehicle, an electric vehicle or a hybrid vehicle.
Advantageous Effects of the Invention
[0010] The lubricating oil composition of the present invention maintains properties necessary
to lubricate a transmission and other devices and has more excellent insulation properties
and anti-wear properties than the prior art and can be improved in anti-seizure properties.
Description of Embodiment
[0011] The present invention will be described in more detail below.
[0012] The lubricating base oil referred to as Component (A) used in the present invention
may be a mineral base oil and/or a synthetic base oil or alternatively a mixture of
two or more types of mineral oils or synthetic base oils, or a mixture of a mineral
base oil and a synthetic base oil. The mix ratio in these mixtures may be selected
arbitrarily.
[0013] Examples of the mineral lubricating base oil which may be used in the present invention
include paraffinic or naphthenic mineral base oils which can be produced by subjecting
a lubricating oil fraction produced by atmospheric- or vacuum-distillation of a crude
oil, to any one of or any suitable combination of refining processes selected from
solvent deasphalting, solvent extraction, hydrocracking, solvent dewaxing, catalytic
dewaxing, hydrorefining, sulfuric acid treatment, and clay treatment; n-paraffins;
and iso-paraffins. These base oils may be used alone or in combination at an arbitrary
ratio.
[0014] Examples of preferred mineral lubricating base oils include the following base oils:
- (1) a distillate oil produced by atmospheric distillation of a paraffin base crude
all and/or a mixed base crude oil;
- (2) a whole vacuum gas oil (WVGO) produced by vacuum distillation of the topped crude
of a paraffin base crude oil and/or a mixed base crude oil;
- (3) a wax produced by a lubricating oil dewaxing process and/or a Fischer-Tropsch
wax produced by a GTL process;
- (4) an oil produced by mild-hydrocracking (MHC) one or more oils selected from oils
of (1) to (3) above;
- (5) a mixed oil of two or more oils selected from (1) to (4) above;
- (6) a deasphalted oil (DAO) produced by deasphalting an oil of (1), (2) (3), (4) or
(5);
- (7) an oil produced by mild-hydrocracking (MHC) an oil of (6); and
- (8) a lubricating oil produced by subjecting a mixed oil of two or more oils selected
from (1) to (7) used as a feed stock and/or a lubricating oil fraction recovered therefrom
to a normal refining process and further recovering a lubricating oil fraction from
the refined product.
[0015] No particular limitation is imposed on the normal refining process used herein. Therefore,
there may be used any refining process having been conventionally used upon production
of a lubricating base oil. Examples of the normal refining process include (a) hydro-refining
processes such as hydrocracking and hydrofinishing, (b) solvent refining such as furfural
extraction, (c) dewaxing such as solvent dewaxing and catalytic dewaxing, (d) clay
refining with acidic clay or active clay and (e) chemical (acid or alkali) refining
such as sulfuric acid treatment and sodium hydroxide treatment. In the present invention,
any one or more of these refining processes may be used in any combination and order.
[0016] The mineral lubricating base oil used in the present invention is particularly preferably
a base oil produced by further subjecting a base oil selected from (1) to (8) described
above to the following treatments.
[0017] That is, preferred are a hydrocracked mineral oil and/or wax-isomerized isoparaffinic
base oil produced by hydrocracking or wax-isomerizing a base oil selected from (1)
to (8) described above as it is or a lubricating fraction recovered therefrom and
subjecting the resulting product as it is or a lubricating fraction recovered therefrom
to dewaxing such as solvent dewaxing or catalytic dewaxing, followed by solvent refining
or followed by solvent refining and then dewaxing such as solvent dewaxing or catalytic
dewaxing. The hydrocracked mineral oil and/or wax-isomerized isoparaffinic base oil
are used in an amount of preferably 30 percent by mass or more, more preferably 50
percent by mass or more, and particularly preferably 70 percent by mass or more, on
the total base oil mass basis.
[0018] The lubricating base oil referred to as Component (A) used in the transmission lubricating
oil composition of the present invention is a lubricating base oil adjusted so that
the 100°C kinematic viscosity is from 1.5 to 4.5 mm
2/s.
[0019] Component (A) is preferably one or more types selected from the following (A-a) to
(A-c):
(A-a) a mineral base oil having a 100°C kinematic viscosity of between 1.5 and lower
than 3.5
mm2/s, preferably 1.9 to 3.2 mm2/s;
(A-b) a mineral base oil having a 100°C kinematic viscosity of between 3.5 and lower
than 7 mm2/s, preferably 3.6 to 4.5 mm2/s; and
(A-c) a synthetic base oil having a 100°C kinematic viscosity of between 1.5 and lower
than 7 mm2/s, preferably 3.8 to 4.5 mm2/s.
[0020] Mineral base oils (A-a) to (A-b) have a %C
A of preferably 2 or less, more preferably 1 or less, more preferably 0.5 or less,
particularly preferably substantially 0. Lubricating oil (A-c) has a %C
A of substantially 0. The use of lubricating base oil (A) having a %C
A of 2 or less renders it possible to produce a lubricating oil composition with an
excellent oxidation stability.
[0021] The %C
A used herein denotes the percentage of the aromatic carbon number in the total carbon
number, determined in accordance with ASTM D 3238-85.
[0022] No particular limitation is imposed on the viscosity index of lubricating base oils
(A-a) to (A-c), which is, however, preferably 80 or greater, more preferably 100 or
greater, particularly preferably 120 or greater and usually 200 or less, preferably
160 or less. The use of a lubricating base oil having a viscosity index of greater
than 80 renders it possible to produce a composition exhibiting excellent viscosity
characteristics from low temperatures to high temperatures. The use of a lubricating
base oil having a too high viscosity index results in a too much normal paraffins
in the resulting composition and also deteriorates the low temperature fluidity thereof.
[0023] No particular limitation is imposed on the sulfur content of mineral base oils (A-a)
to (A-b) used in the present invention, which is, however, preferably 0.05 percent
by mass or less, more preferably 0.02 percent by mass or less, particularly preferably
0.005 percent by mass or less. The sulfur content of lubricating base oil (A-c) is
substantially 0%. Reduction of the sulfur content of Component (A) renders it possible
to produce a composition having a more excellent oxidation stability.
[0024] In the present invention, any one or more of the above-described base oils (A-a)
to (A-c) may be used. Above all, preferably (A-a) and (A-b)and/or(A-c) are used in
combination. When Component (A-a) and/or Component (A-b) and Component (A-c) are used
in combination, the content of Component (A-c) is preferably 1 to 50 percent by mass,
more preferably 3 to 20 percent by mass, more preferably 3 to 10 percent by mass on
the total base oil mass basis. In particular, blending of Component (A-c) in an amount
of on the order of 3 to 10 percent by mass renders it possible to produce a composition
exhibiting excellent effects in fatigue life, low temperature characteristics, and
oxidation stability at a low cost.
[0025] Lubricating base oil (A) used in the present invention has a 100°C kinematic viscosity
of preferably 1.5 to 4.5 mm
2/s, more preferably 2.8 to 4.0 mm
2/s, particularly preferably 3.6 to 3.9 mm
2/s. The use of a lubricating base oil with a 100°C kinematic viscosity of 4.5 mm
2/s or lower renders it possible to produce a lubricating oil composition having a
smaller frictional resistance at lubricating sites because of its small fluid resistance
and thus having excellent low temperature viscosity (for example, the -40°C Brookfield
viscosity is 20,000 Pa·s or less). The use of a lubricating base oil with a 100°C
kinematic viscosity of 1.5 mm
2/s or higher renders it possible to produce a lubricating oil composition which is
sufficient in oil film formation and thus more excellent in lubricity and less in
evaporation loss of the base oil under elevated temperature conditions.
[0026] The synthetic oil referred to as (A-c) may be a synthetic lubricating oil such as
poly-α-olefins (1-octene oligomer, 1-decene oligomer, ethylene-propylene cooligomer)
and hydrogenated compounds thereof; isobutene oligomers and hydrogenated compounds
thereof; isoparaffins; alkylbenzenes; alkylnaphthalenes; alkyldiphenyl ethanes; monoisopropyl
biphenyl; dimethyl silicone; diesters (ditridecyl glutarate, di-2-ethylhexyl adipate,
diisodecyl adipate, ditridecyl adipate and di-2-ethylhexyl sebacate); polyol esters
(trimethylolpropane caprylate, trimethylolpropane pelargonate, pentaerythritol 2-ethylhexanoate
and pentaerythritol pelargonate); polyoxyalkylene glycols; dialkyldiphenyl ethers;
polyphenyl ethers; or a mixture thereof. Among these oils, preferably used are poly-α-olefins
and hydrogenated compounds thereof; isobutene oligomers and hydrogenated compounds
thereof; isoparaffins; alkylbenzenes; alkylnaphthalenes; alkyldiphenylethane; monoisopropyl
biphenyl; and dimethyl silicone because they have a 80°C volume resistivity of 1×10
13 Ω·m or greater and thus can enhance the insulation properties of the resulting lubricating
oil composition. In general, ester-based compounds have a 80°C volume resistivity
of on the order of 1×10
9 to 1×10
13 Ω·m and are preferably those from which the remaining moisture and impurities have
been sufficiently removed.
[0027] The term "80°C volume resistivity" used herein is measured in accordance with JIS
C 2101 24.(volume resistivity test).
[0028] The synthetic oil used in the present invention is preferably selected from poly-α-olefins
and hydrogenated compounds thereof, alkylbenzenes, ester-based compounds and mixtures
thereof. In this case, the resulting composition can maintain low temperature fluidity
and low volatility in well-balance under the conditions where it is used.
[0029] Typical examples of poly-α-olefins include oligomers or cooligomers of α-olefins
having 2 to 32, preferably 6 to 16 carbon atoms, such as 1-octene oligomer, 1-decene
oligomer, ethylene-propylene cooligomer, and hydrogenated compounds thereof.
[0030] These synthetic oils may be used alone. No particular limitation is imposed on the
viscosity thereof. However, synthetic oils with different viscosities may be used
in combination so that the 100°C kinematic viscosity is adjusted to preferably from
1.5 to 4.5 mm
2/s. This is because the combination of a synthetic oil having a high viscosity with
that of a low viscosity results in a base oil having a higher viscosity index.
[0031] The lubricating oil base oil referred to as Component (A) in the present invention
is as described above but is preferably mixed with a solvent refined base oil having
a kinematic viscosity of 20 mm
2/s to 50 mm
2/s if the resulting composition has a problem in fatigue life. Furthermore, it is
preferably mixed with such a solvent refined oil in such an extent that the mixture
is adjusted to have a %C
A of 2 or less and a 100°C kinematic viscosity of 1.5 to 4.5 mm
2/s.
[0032] The lubricating oil composition of the present invention contains (B) at least one
type of phosphorus compound selected from phosphorus compounds having at least one
hydroxyl group and/or at least one thiol group.
[0033] The phosphorus compound referred to as Component (B) in the present invention is
at least one type of compound selected from phosphorus compounds represented by formula
(1), phosphorus compounds represented by formula (2), amine salts thereof, and derivatives
thereof.

[0034] In formula (1), X
1, X
2 and X
3 are each independently oxygen or sulfur and at least one of them is preferably oxygen,
at least one of R
1, R
2 and R
3 is hydrogen and the others are hydrocarbon groups having 1 to 30 carbon atoms.

[0035] In formula (2), X
4, X
5, X
6 and X
7 are each independently oxygen or sulfur (one or two of X
4, X
5 and X
6 may be a single bond or (poly) oxyalkylene group) and at least one of them is preferably
oxygen, at least one of R
4, R
5 and R
6 is hydrogen and the others are hydrocarbon groups having 1 to 30 carbon atoms.
[0036] Examples of the hydrocarbon groups having 1 to 30 carbon atoms for R
1 to R
6 include alkyl, cycloalkyl, alkenyl, alkyl-substituted cycloalkyl, aryl, alkyl-substituted
aryl, and arylalkyl groups. The hydrocarbon groups are preferably alkyl groups having
1 to 30 carbon atoms and aryl groups having 6 to 24 carbon atoms, more preferably
alkyl groups having 3 to 18 carbon atoms, more preferably alkyl groups having 4 to
12 carbon atoms.
[0037] Examples of phosphorus compounds represented by formula (1) include phosphorous acid;
monothiophosphorous acid; dithiophosphorous acid; phosphorous acid monoesters, monothiophosphorous
acid monoesters, dithiophosphorous acid monoesters, and trithiophosphorous acid monoesters,
each having any one of the above-described hydrocarbon groups having 1 to 30 carbon
atoms; and phosphorous acid diesters, monothiophosphorous acid diesters, dithiophosphorous
acid diesters, and trithsophosphorous acid diesters, each having any two of the above-described
hydrocarbon groups having 1 to 30 carbon atoms; and a mixture thereof.
[0038] In order to further enhance the properties such as high temperature detergency and
oxidation stability in the present invention, preferably two or more, particularly
preferably all of X
1 to X
3 in formula (1) are oxygen.
[0039] Examples of phosphorus compounds represented by formula (2) include phosphoric acid;
monothiophosphoric acid; dithiophosphoric acid; trithiophosphoric acid; tetrathiophosphoric
acid; phosphoric acid monoesters, monothiophospharic acid monoesters, dithiophosphoric
acid monoesters, trithiophosphoric acid monoesters, and tetrathiophosphoric acid monoesters,
each having any one of the above-described hydrocarbon groups having 1 to 30 carbon
atoms; phosphoric acid diesters, monothiophosphoric acid diesters, dithiophosphoric
acid diesters, trithiophosphoric acid diesters, and tetrathiophosphoric acid diesters,
each having any two of the above-described hydrocarbon groups having 1 to 30 carbon
atoms; phosphonic acid, phosphonic acid monoesters, and phosphonic acid diesters,
each having any one or two of the above-described hydrocarbon groups having 1 to 30
carbon atoms; the phosphoric acid compounds exemplified above but having a (poly)oxyalkylene
group having 1 to 4 carbon atoms; derivatives of the phosphorus compounds exemplified
above, such as β-dithiophosphorylated propionic acid and reaction products of dithiophosphates
and olefin cyclopentadiene or (methyl)methacrylates; and mixtures thereof.
[0040] In order to further enhance the properties such as high temperature detergency and
oxidation stability in the present invention, preferably two or more, more preferably
three or more, particularly preferably all of X
4 to X
7 in formula (2) are oxygen. One or two of X
4, X
5 and X
6 may be a single bond or a (poly)oxyalkylene group.
[0041] Examples of the salts of phosphorus compounds represented by formula (1) or (2) include
salts produced by allowing a nitrogen compound such as ammonia or an amine compound
having in its molecules only a hydrocarbon group having 1 to 30 carbon atoms or a
hydroxyl group-containing hydrocarbon group having 1 to 30 carbon atoms to react with
a phosphorus compound and neutralize the whole or part of the remaining acid hydrogen.
[0042] Specific examples of the nitrogen-containing compound include ammonia, monoamines,
diamines, and polyamines. Preferred examples include aliphatic amines having an alkyl
or alkenyl group having 10 to 20 carbon atoms, which may be straight-chain or branched,
such as decylamine, dodecylamine, dimethyldodecylamine, tridecylamine, heptadecylamine,
octadecylamine, oleylamine, and stearyl amine.
[0043] The phosphorus compound referred to as Component (B) is preferably at least one type
of compound selected from the group consisting of amine salts of phosphorus compounds
of formula (1) wherein all of X
1, X
2 and X
3 are oxygen and amine salts of phosphorus compounds of formula (2) wherein all of
X
4, x
5, X
6 and X
7 are oxygen (one or two of X
4, and X
6 may be a single bond or a (poly) oxyalkylene group) because they are excellent in
oxidation stability.
[0044] Alternatively, the phosphorus compound referred to as Component (B) is preferably
a phosphorus compound of formula (2) wherein all of X
4, X
5, X
6 and X
7 are oxygen (one or two of X
4, X
5 and X
6 may be a single bond or a (poly)oxyalkylene group), at least one of R
4, R
5 and R
6 is hydrogen and the others are each independently a hydrocarbon group having 1 to
30 carbon atoms in terms of oxidation stability.
[0045] The hydrocarbon group of the phosphorus compound referred to as Component (B) has
preferably 16 or fewer carbon atoms. This is based on the fact that fewer the carbon
atoms, higher the volume resistivity is as set forth in Table 1 below.
[0046]
[Table 1]
| Structure of phosphorus compound |
Trialkyl phosphite |
Dialkylhydrogen phosphine |
Diphenylhydrogen phosphine |
Dialkyl acid phosphate |
| Structure of hydrocarbon group |
iC8 |
nC12 |
nC18 |
iC4 |
iC8 |
nC18 |
phenyl |
nC10 |
nC18 |
| Carnbon number of hydrocarbon group |
8 |
12 |
18 |
4 |
8 |
18 |
6 |
10 |
18 |
| Volume resistivity 1010 Ω·m |
358 |
315 |
27.9 |
1200 |
104 |
12.8 |
800 |
1.44 |
1.4 |
*Phosphoric compounds were each dissolved in a base oil with the following physical
properties to compare the volume resistivity.
They were each added in an amount of 100 mass ppm by phosphorus.
Kinematic viscosity (40°C) 19.7mm2/s, Kinematic viscosity (100°C) 4.3mm2/s, Viscosity index 125, %CP 78.5, %CN21.5, %CA0 |
[0047] In Table 1, the volume resistivity designates the value measured at an oil temperature
of 80°C in accordance with JIS C 2101 24. (volume resistivity test). In the above
examples, each of the phosphorus compound was added and dissolved in a mineral base
oil so that it is contained in an amount of 100 mass ppm on the basis of phosphorus.
[0048] No particular limitation is imposed on the content of Component (B) that is the above-described
phosphorus compound of the lubricating oil composition of the present invention, which
is, however, 0.01 percent by mass or more, preferably 0.02 percent by mass or more,
particularly preferably 0.03 percent by mass or more and preferably 0.1 percent by
mass or less, more preferably 0.08 percent by mass or less, particularly preferably
0.05 percent by mass or less on the basis of phosphorus on the composition mass basis.
If the content of the phosphorus compound is less than 0.01 percent by mass on the
basis of phosphorus, the resulting composition would be less effective in anti-wear
properties. Whilst, if the content of the phosphorus compound is more than 0.1 percent
by mass on the basis of phosphorus, the resulting composition would be poor in insulation
properties, degraded in oxidation stability and enhanced in aggressivity against sealing
materials.
[0049] The lubricating oil composition of the present invention is characterized in that
it contains (C) an ashless dispersant having a functional group containing nitrogen
as a dispersion group in an amount of less than 0.001 percent by mass on the basis
of nitrogen on the composition mass basis or does not contain such an ashless dispersant
at all.
[0050] As described above, the lubricating oil composition of the present invention contains
(B) at least one type of phosphorus compound selected from phosphorus compounds having
at least one hydroxyl group and/or at least one thiol group. The inclusion of the
phosphorus compound enhances significantly the anti-wear properties and anti-seizure
properties of the composition. However, this type of phosphorus compound degrades
drastically the volume resistance of the composition compared with a phosphorus compound
having no hydroxyl group and/or thiol group if an ashless dispersant having a functional
group containing nitrogen as a dispersion group is contained. Therefore, the composition
contains necessarily (C) an ashless dispersant having a functional group containing
nitrogen as a dispersion group in an amount of less than 0.001 percent by mass on
the basis of nitrogen on the composition mass basis or does not contain such an ashless
dispersant at all in order to improve the anti-wear properties and anti-seizure properties
of the composition.
[0051] Examples of the ashless dispersant having a functional group containing nitrogen
as a dispersion group referred to as Component (C) include succinimide, benzylamine,
and polyamines, each having a hydrocarbon group having 40 to 400 carbon atoms.
[0052] However, among these compounds, those having been modified to have a structure wherein
nitrogen cannot constitute a salt structure together with Component (B) that is the
phosphorus compound are excluded from the examples. Fox example, compounds wherein
the amino group is acylated or modified with a boron compound or a sulfuric compound
and incapable of constituting a salt structure with Component (B) that is the phosphorus
compound are excluded.
[0053] What is meant by "containing an ashless dispersant having a functional group containing
nitrogen as a dispersion group in an amount of less than 0.001 percent by mass on
the basis of nitrogen on the composition mass basis" is a structure or amount wherein
even though an ashless dispersant has an amino group remained so as to be able to
constitute a salt structure with Component (B) that is the phosphorus compound, the
content thereof is such a level that the volume resistance at 80°C of the resulting
composition is 5×10
8 Ω·m or greater. Specifically, the ashless dispersant is contained in such an amount
that nitrogen is contained in an amount of less than 0.001 percent by mass, more preferably
less than 0.0008 percent by mass on the composition mass basis.
[0054] No particular limitation is imposed on the use of compounds with a structure of thiadiazole
or triazole that is an amine-based anti-oxidant or a corrosion inhibitor because it
can be ignored if the content thereof is 1 percent by mass or less.
[0055] The lubricating oil composition of the present invention has a 80°C volume resistivity
of preferably 5×10
8 Ω·m or greater, more preferably 6×10
8 Ω·m or greater, particularly preferably 10x10
8 Ω·m or greater. The composition having a 80°C volume resistivity of 5×10
8 Ω·m or greater can keep the insulation properties high not only when it is fresh
but also when it is degraded thereby avoiding an electric motor from having a trouble
such as shorting out for a long period of time.
[0056] If necessary, the lubricating oil composition of the present invention may be blended
with various additives such as viscosity index improvers, extreme pressure additives,
dispersants other than the above-described dispersant compounds, metallic detergents,
friction modifiers, anti-oxidants, corrosion inhibitors, rust inhibitors, demulsifiers,
metal deactivators, pour point depressants, seal swelling agents, anti-foaming agents,
and dyes, alone or in combination in order to further enhance the properties of the
composition or impart the composition with properties required for a lubricating oil.
[0057] Examples of the viscosity index improvers include non-dispersant or dispersant type
poly(meth)acrylate; non-dispersant or dispersant type ethylene-α-olefin copolymers
and hydrogenated compounds thereof; polyisobutylene and hydrogenated compounds thereof;
styrene-diene hydrogenated copolymers; styrene-maleic anhydride ester copolymers;
polyalkylstyrenes; and copolymers of (meth) acrylate monomers represented by formula
(1) and unsaturated monomers such as ethylene/propylene/styrene/maleic anhydride.
[0058] The amount of the viscosity index improver in the lubricating oil composition of
the present invention is such an amount that the resulting composition has a 100°C
kinematic viscosity of 5 to 10 mm
2/s, preferably 6 to 9 mm
2/s and a viscosity index of 120 to 270, preferably 150 to 250, more preferably 170
to 220. More specifically, the amount is 15 percent by mass or less, preferably 10
percent by mass or less, more preferably 8 percent by mass or less and 2 percent by
mass or more, preferably 4 percent by mass or more, more preferably 5 percent by mass
or more on the composition mass basis. An amount of more than 15 percent by mass causes
a too high viscosity while an amount of less than 2 percent by mass causes a too high
viscosity and thus cannot secure a sufficient composition viscosity.
[0059] Examples of the metallic detergent include those such as alkaline earth metal sulfonates,
alkaline earth metal phenates, and alkaline earth metal salicylates.
[0060] Any one or more compounds selected from these metallic detergents may be contained
in an amount of usually 0.01 to 10 percent by mass, preferably 0.1 to 5 percent by
mass on the total composition mass basis.
[0061] The friction modifier may be any compound that has been generally used as a friction
modifier for lubricating oils. Specific examples include amine compounds, imide compounds,
fatty acid esters, fatty acid amides, and fatty acid metal salts, each having per
molecule at least one alkyl or alkenyl group having 6 to 30 carbon atoms, particularly
a straight-chain alkyl or alkenyl group having 6 to 30 carbon atoms.
[0062] Any one or more compounds selected from these friction modifiers may be contained
in an amount of usually 0.01 to 5.0 percent by mass, preferably 0.03 to 3.0 percent
by mass on the total composition mass basis.
[0063] The anti-oxidant may be any anti-oxidant that has been usually used in lubricating
oils, such as phenol- or amine-based compounds.
[0064] Specific examples of the anti-oxidant include alkylphenols such as 2-6-di-tert-butyl-4-methylphenol;
bisphenols such as methylene-4,4-bisphenol(2,6-di-tert-butyl-4-methylphenol); naphthylamines
such as phenyl-α-naphthylamine; dialkyldiphenylamines; zinc dialkyldithiophosphoric
acids such as di-2-ethylhexyldithiophosphoric acid; and esters of (3,5-di-tert-butyl-4-hydroxyphenyl)fatty
acid (propionic acid) or (3-methyl-5-tert-butyl-4-hydroxyphenyl)fatty acid (propionic
acid) with a monohydric or polyhydric alcohol such as methanol, octanol, octadecanol,
1,6-hexanediol, neopentyl glycol, thiodiethylene glycol, triethylene glycol and pentaerythritol.
[0065] Any one or more of compounds selected from these compounds may be contained in any
amount, which is, however, usually from 0.01 to 5 percent by mass, preferably from
0.1 to 3 percent by mass on the total composition mass basis.
[0066] Examples of the corrosion inhibitor include benzotriazole-, tolyltriazole-, thiadiazole-,
and imidazole-types compounds.
[0067] Examples of the rust inhibitor include petroleum sulfonates, alkylbenzene sulfonates,
dinonylnaphthalene sulfonates, alkenyl succinic acid esters, and polyhydric alcohol
esters.
[0068] Examples of the demulsifier include polyalkylene glycol-based non-ionic surfactants
such as polyoxyethylenealkyl ethers, polyoxyethylenealkylphenyl ethers, and polyoxyethylenealkylnaphthyl
ethers.
[0069] Examples of the metal deactivator include imidazolines, pyrimidine derivatives, alkylthiadiazoles,
mercaptobenzothiazoles, benzotriazoles and derivatives thereof, 1,3,4-thiadiazolepolysulfide,
1,3,4-thiadiazolyl-2,5-bisdialkyldithiocarbamate, 2-(alkyldithio)benzoimidazole, and
β-(o-carboxybenzylthio)propionitrile.
[0070] The pour point depressant may be any of the known pour point depressants selected
depending on the type of lubricating base oil but are preferably poly(meth)acrylates
having a weight average molecular weight of preferably 20, 000 to 500,000, more preferably
50,000 to 300,000, particularly preferably 80,000 to 200,000.
[0071] The anti-foaming agent may be any compound that has been usually used as an anti-foaming
agent for lubricating oils. Examples of such an anti-foaming agent include silicones
such as dimethylsilicone and fluorosilicone. Any one or more of compounds selected
from these compounds may be contained in any amount.
[0072] The seal swelling agent may be any compound that has been usually used as a seal
swelling agent for lubricating oils. Examples of such a seal swelling agents include
ester-, sulfur- and aromatic-based seal swelling agents.
[0073] The dye may be any compound that has been usually used and may be blended in any
amount. The amount is usually from 0.001 to 1.0 percent by mass on the total composition
mass basis.
[0074] When these additives are blended with the lubricating oil composition of the present
invention, the corrosion inhibitor, rust inhibitor, and anti-foaming agent are each
contained in an amount of 0.005 to 5 percent by mass, the pour point depressant and
metal deactivator are each contained in an amount of 0.005 to 2 percent by mass, the
seal swelling agent is contained in an amount of 0.01 to 5 percent by mass, and the
anti-foaming agent is contained in an amount of 0.0005 to 1 percent by mass, all on
the total composition mass basis.
Examples
[0075] The present invention will be described more specifically with reference to the following
Examples and Comparative Examples but not limited thereto.
[0076] (Examples 1 to 6 and Comparative Examples 1 to 5)
[0077] Lubricating oil compositions according to the present invention (Examples 1 to 6)
and those for comparison (Comparative Examples 1 to 5) were prepared in accordance
with the formulations set forth in Table 2. The performances of each composition were
evaluated with the following tests. The results are set forth in Table 2.
[Table 2]
| Base Oil |
Total Base Oil Mass Basis |
|
Example |
Example 2 |
Example 3 |
Example 4 |
Example 5 |
Example 6 |
Comparative Example 1 |
Comparative Example 2 |
Comparative Example 3 |
Comparative Example 4 |
Comparative Example 5 |
| A-1 |
Base Oil 1 1) |
inmass% |
100 |
100 |
|
|
100 |
100 |
100 |
100 |
100 |
100 |
100 |
| A-2 |
Base Oil 2 2) |
inmass% |
|
|
100 |
|
|
|
|
|
|
|
|
| A-3 |
Base Oil 3 3) |
inmass% |
|
|
|
100 |
|
|
|
|
|
|
|
| Additives |
Total Composition Mass Basis |
mass% |
|
|
|
|
|
|
|
|
|
|
|
| B-1 |
Oil soluble phosphorus additive 1 4) |
mass% |
0.5 |
0.1 |
0.1 |
0.1 |
|
|
|
0.1 |
|
0.1 |
|
| B-2 |
Oil soluble phosphorus additive 2 5) |
mass% |
|
|
|
|
0.1 |
|
|
|
|
|
|
| B-3 |
Oil soluble phosphorus additive 3 6) |
mass% |
|
|
|
|
|
0.1 |
|
|
|
|
|
| B-4 |
Oil soluble phosphorus additive 4 7) |
|
|
|
|
|
|
|
|
|
|
|
0.3 |
| C-1 |
Ashless dispersant 1 8) |
mass% |
|
|
|
|
|
|
|
4 |
4 |
|
|
| C-2 |
Ashless dispersant 2 9) |
|
|
|
|
|
|
|
|
|
|
4 |
|
| D-1 |
Viscosity index improver 10) |
mass% |
12 |
12 |
12 |
17 |
12 |
12 |
12 |
12 |
12 |
12 |
12 |
| |
Additive package 11) |
mass% |
2.5 |
2.5 |
2.5 |
2.5 |
2.5 |
2.5 |
2.5 |
2.5 |
25 |
2.5 |
2.5 |
| P content of the composition |
masspm |
500 |
100 |
100 |
100 |
100 |
100 |
0 |
100 |
0 |
100 |
100 |
| Evalution results |
|
|
|
|
|
|
|
|
|
|
|
|
| Four - ball test 12) |
|
|
|
|
|
|
|
|
|
|
|
|
| WL |
mm2/s |
1961 |
1961 |
1961 |
1961 |
1961 |
1961 |
1961 |
1961 |
1961 |
1961 |
1961 |
| LNSL |
% |
785 |
785 |
785 |
785 |
785 |
785 |
490 |
785 |
490 |
785 |
785 |
| Four- ball (wear scar diameter) 13) |
mm2/s |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.7 |
0.5 |
0.8 |
0.5 |
0.5 |
| Volume resistivity 14) |
1010 Ω·m |
0.06 |
0.15 |
0.12 |
0.06 |
0.13 |
0.05 |
0.16 |
0.005 |
0.031 |
0.001 |
0.01 |
1) kinematic viscosity (40°C) 19.7mm2/s. kinematic viscosity (100°C) 4.3mm2/s, viscosity index 125, %CP 78.5, %CN 21.5, %CA 0
2) kinematic viscosity (40°C) 22.7mm2/s, kinematic viscosity (100°C) 4.3mm2/s, viscosity index 102, %CP 66.4, %CN 29.0, %CA4.6
3) di-2-ethylhexyl azelate kinematic viscosity (40°C) 10.1mm2/s. kinematic viscosity (100°C) 3.0mm2/s, viscosity index 144
4) amine salt of acidic phosphoric acid ester (P content: 10%, phosphoric acid ester:
2-ethylhexyl, amine: mixed amine of C11 to 14)
5) hydrogen phosphine, isoC4 P content 16%
6) acidic phosphoric acid ester, 2-ethylhexyl P: 9.4%
7) trioleylphosphite P: 3.7%
8) boronated succinimide, PIS Mw 2000, bis type, TEPA crosslinking
9) succinimide, PIB Mw 1000, bis type. TEPA crosslinking
10) non-dispersant type PMA Mw 25,000
11) containing Ca metallic detergent (0.1 mass%), metal deactivator (0.1 mass%), anti-oxidant
(2.0 mass%), anti-foaming agent (30 mass ppm)
12) 1800 rpm
13) 392 N, 1800 rpm, 80°C, 30 min
14) in accordance with JIS C2101, measured at 80°C |
Applicability in Industry
[0078] The lubricating oil composition of the present invention is a composition improved
in anti-wear properties and anti-seizure properties and can be used as a lubricating
oil for an electric motor-equipped vehicle such as an electric vehicle or a hybrid
vehicle, an electric motor oil, an oil both for a transmission and an electric motor,
and an oil for a device wherein a transmission and an electric motor are packaged
in one and a lubricating system is shared by the transmission and an electric motor.
[0079] The present invention can provide the above-described transmission, electric motor
and device including the lubricating oil composition of the present invention and
a method for lubricating, insulating and cooling the above-described transmission,
electric motor and device using the lubricating oil composition of the present invention.