Patent Grant
10815445
This application is a 371 of PCT/JP2017/008255, filed Mar. 2, 2017. This application is based upon and claims the benefit of priority to Japanese Application No. 2016-042504, which was filed on Mar. 4, 2016.
The present invention relates to a lubricating oil composition, and to a lubrication method and a transmission using the lubricating oil composition.
Recently, with the increase in the consciousness of environmental issues, requirements for fuel saving in various technical fields are being severer, for the purpose of more effective use of oil resources and reduction in CO2 emission. For example, for lubricating oil compositions for use in transmissions, requirements for fuel saving are increasing. PTL 1 proposes a lubricating oil composition obtained by blending two kinds of polymethacrylates differing in the molecular weight with the base oil.
PTL 1: JP 2015-172165 A
For attaining fuel saving, for example, a lubricating oil composition for transmissions is required to satisfy the characteristics that the viscosity thereof hardly increases so as not to increase too much the stirring resistance at low temperatures but that, on the other hand, the viscosity thereof hardly decreases so as to sufficiently maintain an oil film at high temperatures. The viscosity characteristics can be attained, for example, by increasing the viscosity index of a lubricating oil composition, and a viscosity index improver such as polymethacrylate as described in PTL 1 is used.
The viscosity index improving performance of a viscosity index improver generally bears a proportional relationship to the mean molecular weight thereof, and the performance tends to increase with the increase in the mean molecular weight. On the other hand, when having a large mean molecular weight, the molecular chain of the viscosity index improver may be cut owing to the mechanical shear force to be given to the lubricating oil composition during use so that the performance thereof may lower with the result that the viscosity of the lubricating oil composition lowers and an oil film could not be sufficiently maintained and therefore the performance of the lubricating oil composition worsens. Specifically, it may be said that a high viscosity index and high shear stability are contradictory to each other.
For attaining high fuel saving performance, a lubricating oil composition is required to satisfy both the contradictory properties of high viscosity index and high shear stability. However, the viscosity index improver such as a polymethacrylate as used in PTL 1 could hardly satisfy both the contradictory properties on a higher level.
The present invention has been made in consideration of the above-mentioned situation, and its object is to provide a lubricating oil composition satisfying both the requirements of high viscosity index and high shear stability, and to provide a lubrication method and a transmission using the lubricating oil composition.
As a result of assiduous studies, the present inventor has found that the following invention can solve the above-mentioned problems. Specifically, the present invention provides a lubricating oil composition having the constitution mentioned below, and a lubrication method and a transmission using the lubricating oil composition.
1. A lubricating oil composition containing a synthetic oil (1) having a kinematic viscosity at 100° C. of 2.5 mm2/s or less, and a polymethacrylate (2) having a monovalent functional group containing an oxygen atom in the molecule, which has a structural unit represented by the following general formula (I):
wherein R1 represents a divalent aliphatic hydrocarbon group having 24 to 40 carbon atoms, and X1 represents a monovalent functional group containing an oxygen atom.
2. A lubrication method using the lubricating oil composition of the above 1.
3. A transmission using the lubricating oil composition of the above 1.
According to the present invention, there are provided a lubricating oil composition that satisfies both high viscosity index and high shear stability, and a lubrication method and a transmission using the lubricating oil composition.
Hereinunder, embodiments of the present invention (also referred to as “the present embodiments”) are described. In this description, the numerical values regarding “or more” and “or less” relating to the description of a numerical value range are values that can be combined arbitrarily.
[Lubricating Oil Composition]
The lubricating oil composition of the present embodiment is a lubricating oil composition containing a synthetic oil (1) having a kinematic viscosity at 100° C. of 2.5 mm2/s or less (hereinafter may be referred to as “synthetic oil (1)”), and a polymethacrylate (2) having a functional group containing an oxygen atom in the molecule, which has a structural unit represented by the above-mentioned general formula (I) (hereinafter may be referred to as “polymethacrylate (2)”). Each component is described below.
(Synthetic Oil (1))
With no specific limitation thereon, the synthetic oil (1) may be any synthetic oil whose kinematic viscosity at 100° C. falls within the above-mentioned range. Examples of the synthetic oil include poly-α-olefins such as polybutene, ethylene-α-olefin copolymers, and α-olefin homopolymers or copolymer; various esters such as polyol esters, dibasic acid esters, and phosphate esters; various ethers such as polyphenyl ethers; polyglycols; alkylbenzenes; and alkylnaphthalenes. One of these synthetic oils may be used alone or plural kinds thereof may be used in combination.
Above all, from the viewpoint of readily satisfying both high viscosity index and high shear stability, poly-α-olefins are preferred.
The kinematic viscosity at 100° C. of the synthetic oil (1) is 2.5 mm2/s or less. Using one whose kinematic viscosity at 100° C. falls within the above-mentioned range can readily satisfy both high viscosity index and high shear stability. From the same viewpoint, the kinematic viscosity at 100° C. of the synthetic oil (1) is preferably 2.3 mm2/s or less, more preferably 2.2 mm2/s or less. The lower limit of the kinematic viscosity at 100° C. of the synthetic oil (1) is not specifically limited, but is preferably 0.5 mm2/s or more, more preferably 0.7 mm2/s or more, even more preferably 0.8 mm2/s or more.
The kinematic viscosity at 40° C. of the synthetic oil (1) is preferably 1 mm2/s or more, more preferably 1.5 mm2/s or more, even more preferably 2 mm2/s or more. The upper limit is preferably 10 mm2/s or less, more preferably 9 mm2/s or less, even more preferably 8 mm2/s or less. Using the synthetic oil (1) whose kinematic viscosity at 40° C. falls within the above-mentioned range can readily satisfy both high viscosity index and high shear stability.
Also from the viewpoint of readily attaining both high viscosity index and high shear stability, the viscosity index of the synthetic oil (1) is preferably 90 or more, more preferably 100 or more, even more preferably 110 or more.
Here, the kinematic viscosity and the viscosity index are values measured using a glass capillary viscometer according to JIS K 2283:2000.
The content of the synthetic oil (1) based on the total amount of the lubricating oil composition is generally 50% by mass or more, preferably 55% by mass or more, more preferably 60% by mass or more, even more preferably 65% by mass or more. The upper limit is preferably 97% by mass or less, more preferably 95% by mass or less, even more preferably 90% by mass or less. When the content of the synthetic oil (1) falls within the above range, both high viscosity index and high shear stability can be readily attained.
Topped crudes obtained through atmospheric distillation of crude oils such as paraffin base crude oils, naphthene base crude oils and intermediate base crude oils; distillates obtained through vacuum distillation of such topped crudes; mineral oils obtained by purifying the distillates through one or more purification treatments of solvent deasphalting, solvent extraction, hydrocracking, solvent dewaxing, catalytic dewaxing or hydrorefining, for example, a mineral oil such as a light neutral oil, an intermediate neutral oil, a heavy neutral oil, and a bright stock; and mineral oils obtained through isomerization of wax produced through Fischer-Tropsch synthesis (GTL wax) may also be used within a range not detracting from the advantageous effects of the present invention.
(Polymethacrylate (2))
The polymethacrylate has a structural unit represented by the following general formula (I), and therefore has a monovalent functional group containing an oxygen atom in the molecule.
In the general formula (I), R1 represents a divalent aliphatic hydrocarbon group having 24 to 40 carbon atoms, and X1 represents a monovalent functional group containing an oxygen atom. Here, when the carbon number of R1 is 23 or less, there may occur a problem in point of attaining high viscosity index, and on the other hand, when the carbon number is 41 or more, there may occur a problem in point of attaining high shear stability.
The divalent aliphatic hydrocarbon group having 24 to 40 carbon atoms for R1 includes an alkylene group and an alkenylene group, and from the viewpoint of readily attaining high viscosity index and high shear stability, an alkylene group is preferred. The group may be linear, branched or cyclic, but from the viewpoint of more readily attaining both high viscosity index and high shear stability, a linear or branched group is preferred. Also from the same viewpoint, the carbon number is preferably 28 to 40, more preferably 30 to 40.
Examples of the alkylene group having 24 to 40 carbon atoms include various tetracosylene groups such as an n-tetracosylene group, an isotetracosylene group, and isomers thereof (hereinunder functional groups having predetermined carbon atoms including linear and branched ones and isomers thereof may be abbreviated as various functional groups), various pentacosylene groups, various hexacosylene groups, various heptacosylene groups, various octacosylene groups, various nonacosylene groups, various triacontylene groups, various hentriacontylene groups, various dotriacontylene groups, various tritriacontylene groups, various tetratriacontylene groups, various pentatriacontylene groups, various hexatriacontylene groups, various heptatriacontylene groups, various octatriacontylene groups, various nonatriacontylene groups, and various tetracontylene groups.
In the general formula (I), X1 represents a monovalent functional group containing an oxygen atom. When the substituent is not a monovalent functional group containing an oxygen atom, high viscosity index and high shear stability could not be attained. From the viewpoint of readily attaining both high viscosity index and high shear stability, a hydroxy group, an alkoxy group, an aldehyde group, a carboxy group, an ester group, a nitro group, an amide group, a carbamate group, a sulfo group and the like are preferred; a hydroxy group and an alkoxy group are more preferred; and a hydroxy group is even more preferred. Here, the alkoxy group is preferably one containing an alkyl group having 1 to 30 carbon atoms, and the alkyl group may be linear or branched.
The polymethacrylate (2) may have any other structural unit represented by the following general formula (II) as far as it has the structural unit represented by the above-mentioned general formula (I).
In the general formula (II), R2 represents a divalent aliphatic hydrocarbon group having 1 to 40 carbon atoms, and X2 represents a monovalent functional group.
The divalent aliphatic hydrocarbon group having 1 to 40 carbon atoms for R2 includes, in addition to the divalent aliphatic hydrocarbon group having 24 to 40 carbon atoms exemplified for the above R1, a divalent aliphatic hydrocarbon group having 1 to 23 carbon atoms. The divalent aliphatic hydrocarbon group having 1 to 23 carbon atoms is, from the viewpoint of readily attaining high viscosity index and high shear stability, preferably an alkylene group or an alkenylene group, more preferably an alkylene group. The alkylene group may be linear or branched, and more preferably has 1 to 30 carbon atoms.
Examples of the monofunctional group for X2 include an aryl group such as a phenyl group, a benzyl group, a tolyl group and a xylyl group; a heterocyclic group such as a furanyl group, a thiophenyl group, a pyridinyl group and a carbazolyl group; and an organic group containing a hetero atom represented by the following general formulae (III) to (IV); and when the carbon number of R2 is 1 to 23, the substituent may further include a functional group containing an oxygen atom as exemplified for the above X1, in addition to these monofunctional groups.
In the general formulae (III) and (IV), R3 each independently represents a hydrogen atom, or a monovalent aliphatic hydrocarbon group having 1 to 30 carbon atoms. The monovalent aliphatic hydrocarbon group is, from the viewpoint of readily attaining both high viscosity index and high shear stability, preferably an alkyl group or an alkenyl group, and is more preferably an alkyl group. The monovalent aliphatic hydrocarbon group may be linear or branched.
Having a structural unit represented by the above general formula (I), the polymethacrylate (2) is not specifically limited in point of the proportion of the structural unit, but from the viewpoint of more readily attaining both high viscosity index and high shear stability, the copolymerization ratio of the structural unit represented by the general formula (I) to, for example, any other structural unit than the structural unit represented by the general formula (I) such as the above-mentioned other structural unit (for example, the structural unit represented by the above general formula (II)) is preferably 10/90 to 90/10, more preferably 20/80 to 80/20, even more preferably 30/70 to 70/30.
The mass average molecular weight of the polymethacrylate (2) is preferably 5,000 or more, more preferably 15,000 or more, even more preferably 20,000 or more, especially preferably 25,000 or more. The upper limit is preferably 100,000 or less, more preferably 80,000 or less, even more preferably 70,000 or less, especially preferably 55,000 or less. When the mass average molecular weight of the polymethacrylate (2) falls within the above range, both high viscosity index and high shear stability can be more readily attained.
Here, the mass average molecular weight may be measured through gel permeation chromatography (GPC) and determined from the calibration curve drawn using polystyrene. For example, the mass average molecular weight of each above-mentioned polymer may be calculated as a polystyrene-equivalent value through GPC mentioned below.
<GPC Apparatus>
Column: TOSO GMHHR-H(S)HT
Detector: RI detector for liquid chromatography, WATERS 150 C
<Measurement Conditions>
Solvent: 1,2,4-trichlorobenzene
Measurement temperature: 145° C.
Flow rate: 1.0 ml/min
Sample concentration: 2.2 mg/ml
Injection amount: 160 μl
Calibration curve: Universal Calibration
Analysis program: HT-GPC (Ver. 1.0)
The content of the polymethacrylate (2) based on the total amount of the composition is generally 1% by mass or more, preferably 3% by mass or more, more preferably 5% by mass or more, and the upper limit is generally 20% by mass or less, preferably 15% by mass or less, more preferably 13% by mass or less. When the content of the polymethacrylate (2) falls within the above range, the polymethacrylate addition effect may be sufficiently attained to readily satisfy both high viscosity index and high shear stability.
(Other Additives)
In the lubricating oil composition of the present embodiment, any other additives than the synthetic oil (1) and the polymethacrylate (2), for example, other additive such as a viscosity index improver, an antioxidant, a metal-based detergent, a dispersant, a friction modifier, an anti-wear agent, an extreme-pressure agent, a pour point depressant, a metal deactivator, a rust inhibitor, and an anti-foaming agent may be appropriately selected and blended in the composition within a range not conflicting with the advantageous effects of the present invention. One of these additives may be used singly or plural kinds thereof may be used in combination. The lubricating oil composition of the present embodiment may be composed of the synthetic oil (1) and the polymethacrylate (2) as above, or may be composed of the synthetic oil (1), the polymethacrylate (2) and other additives.
Falling within a range not conflicting with the advantageous effects of the present invention, the total content of the additives is not specifically limited, but is, in consideration of the effect of the additives to be added, preferably 0.1 to 20% by mass based on the total amount of the composition, more preferably 1 to 15% by mass, even more preferably 3 to 15% by mass.
(Viscosity Index Improver)
Examples of the viscosity index improver include polymers such as olefin-based copolymers (for example, ethylene-propylene copolymers), dispersant-type olefin-based copolymers, and styrene-based copolymers (for example, styrene-diene copolymers, and styrene-isoprene copolymers).
(Antioxidant)
Examples of the antioxidant include amine-based antioxidants such as diphenylamine-based antioxidants and naphthylamine-based antioxidants; phenol-based antioxidants such as monophenol-based antioxidants, diphenol-based antioxidants, and hindered phenol-based antioxidants; molybdenum-based antioxidants such as molybdenum amine complex produced through reaction of molybdenum trioxide and/or molybdic acid and an amine compound; sulfur-based antioxidants such as phenothiazine, dioctadecyl sulfide, dilauryl-3,3′-thiodipropionate, and 2-mercaptobenzimidazole; and phosphorus-based antioxidants such as phosphite-based antioxidants such as triphenyl phosphite, diisopropylmonophenyl phosphite, and monobutyldiphenyl phosphite.
(Metal-Based Detergent)
Examples of the metal-based detergent include neutral metal sulfonates, neutral metal phenates, neutral metal salicylates, neutral metal phosphonates, basic metal sulfonates, basic metal phenates, basic metal salicylates, basic metal phosphonates, overbased metal sulfonates, overbased metal phenates, overbased metal salicylates, and overbased phosphonates containing an alkaline earth metal such as calcium as the metal species therein.
(Dispersant)
Examples of the dispersant include ash-free dispersants such as boron-free succinimides, boron-containing succinimides, benzylamines, boron-containing benzylamines, succinates, and mono or dicarboxylic acid amides of typically fatty acids or succinic acid.
(Friction Modifier)
Examples of the friction modifier include ash-free friction modifiers such as fatty acid amines, fatty acid esters, fatty acid amides, fatty acids, aliphatic alcohols, and fatty acid ethers having at least one alkyl or alkenyl group having 6 to 30 carbon atoms, especially a linear alkyl or alkenyl group having 6 to 30 carbon atoms in the molecule; and molybdenum-based friction modifiers such as molybdenum dithiocarbamate (MoDTC), molybdenum dithiophosphate (MoDTP), and molybdic acid amine salts.
(Anti-Wear Agent)
Examples of the anti-wear agent include sulfur-containing compounds such as zinc dialkyldithiophosphates (ZnDTP), zinc phosphate, zinc dithiocarbamate, molybdenum dithiocarbamate, molybdenum dithiophosphate, disulfides, sulfurized olefins, sulfurized oils and fats, sulfurized esters, thiocarbonates, thiocarbamates, and polysulfides; phosphorus-containing compounds such as phosphite esters, phosphate esters, phosphonate esters, and amine salts or metal salts thereof; and sulfur and phosphorus-containing anti-wear agents such as thiophosphite esters, thiophosphate esters, thiophosphonate esters, and amine salts or metal salts thereof.
(Extreme-Pressure Agent)
Examples of the extreme-pressure agent include sulfur-based extreme-pressure agents such as sulfides, sulfoxides, sulfones, and thiophosphinates; halogen-based extreme-pressure agents such as chlorohydrocarbons; and organic metal-based extreme pressure agents.
(Pour Point Depressant)
Examples of the pour point depressant include ethylene-vinyl acetate copolymers, condensates of chloroparaffin and naphthalene, condensates of chloroparaffin and phenol, polymethacrylates, and polyalkylstyrenes.
(Metal Deactivator)
Examples of the metal deactivator include benzotriazole compounds, tolyltriazole compounds, thiadiazole compounds, and imidazole compounds.
(Rust Inhibitor)
Examples of the rust inhibitor include petroleum sulfonates, alkylbenzene sulfonates, dinonylnaphthalene sulfonates, alkenylsuccinates, and polyalcohol esters.
(Anti-Foaming Agent)
Examples of the anti-foaming agent include silicone oils, fluorosilicone oils, and fluoroalkyl ethers.
(Various Properties of Lubricating Oil Composition)
The kinematic viscosity at 100° C. of the lubricating oil composition of the present embodiment is preferably 4 mm2/s or more, more preferably 4.2 mm2/s or more, even more preferably 4.5 mm2/s or more, and is also preferably 7 mm2/s or less, more preferably 6 mm2/s or less, even more preferably 5.5 mm2/s or less. The kinematic viscosity at 40° C. of the lubricating oil composition of the present embodiment is preferably 10 mm2/s or more, more preferably 12 mm2/s or more, even more preferably 13 mm2/s or more, and is also preferably 20 mm2/s or less, more preferably 19 mm2/s or less, even more preferably 18 mm2/s or less.
The viscosity index of the lubricating oil composition of the present embodiment is preferably 260 or more, more preferably 270 or more, even more preferably 275 or more.
Here, the methods for measuring the kinematic viscosity and the viscosity index are the same as those for the base oil mentioned above.
Since the lubricating oil composition of the present embodiment has the above-mentioned kinematic viscosity and having a high viscosity index, the resistance to stirring thereof is low and the viscosity thereof hardly increases at low temperatures, and on the other hand, the viscosity of the composition hardly lowers so as to sufficiently maintain an oil film at high temperatures.
A rate of change in kinematic viscosity at 40° C. of the lubricating oil composition of the present embodiment, as measured according to the method mentioned below, is preferably 5% or less, more preferably 4% or less, even more preferably 3% or less. The rate of change in kinematic viscosity at 40° C. is an index of shear stability that indicates a change of kinematic viscosity before and after ultrasonic treatment, and a smaller rate of change means that the lubricating oil composition is hardly influenced by ultrasonic treatment and has higher shear stability. The lubricating oil composition of the present embodiment has a small rate of change in kinematic viscosity as mentioned above, and can express high shear stability.
(Method for Calculating Rate of Change in Kinematic Viscosity at 40° C.)
With respect to an ultrasonically-treated composition obtained by irradiating a lubricating oil composition with ultrasonic waves for 60 minutes according to JASO M347-95 and an untreated lubricating oil composition, their kinematic viscosity at 40° C. (v1, v0) is measured according to JIS K2283:2000. The rate of reduction ((v0−v1)/v0×100) is referred to as the rate of change in kinematic viscosity at 40° C.
Regarding the lubricating oil composition of the present embodiment, in addition, the kinematic viscosity at 100° C. of the ultrasonically-treated composition and the untreated composition is measured and the rate of change in kinematic viscosity at 100° C. thereof is calculated according to the above-mentioned method (method for calculating rate of change in kinematic viscosity at 40° C.). Preferably, the thus-calculated rate of change is 5% or less, more preferably 4.5% or less, even more preferably 4% or less.
As described above, the lubricating oil composition of the present embodiment satisfies both high viscosity index and high shear stability, and, for example, when applied to transmissions such as those for gasoline vehicles, hybrid vehicles and electric vehicles, the composition secures excellent fuel saving performance and is therefore favorably used for these uses. In addition, the lubricating oil composition is also favorably used for other uses, for example, for internal combustion engines, hydraulic machinery, turbines, compressors, working machines, cutting machines, gears, and machines equipped with liquid bearings or ball bearings.
[Lubrication Method and Transmission]
The lubrication method of the present embodiment is a lubrication method using the lubricating oil composition of the present embodiment described above. The lubricating oil composition for use in the lubrication method of the present embodiment satisfies both high viscosity index and high shear stability. Accordingly, the lubrication method of the present embodiment is favorably used, for example, for transmissions such as those of gasoline vehicles, hybrid vehicles and electric vehicles, and when used in these uses, the method exhibits excellent fuel saving performance. In addition, the lubrication method is also favorably used for other uses, for example, for lubrication of internal combustion engines, hydraulic machinery, turbines, compressors, working machines, cutting machines, gears, and machines equipped with liquid bearings or ball bearings.
The transmission of the present embodiment uses the lubricating oil composition of the present embodiment. The transmission of the present embodiment expresses excellent fuel saving performance and is widely favorably applied to various vehicles such as gasoline vehicles, hybrid vehicles and electric vehicles.
Next, the present invention is described in more detail with reference to Examples, but the present invention is not limited at all by these Examples.
Lubricating oil compositions were prepared at the blending ratio (% by mass) shown in Table 1. The resultant lubricating oil compositions were tested variously according to the methods mentioned below to evaluate the properties thereof. The evaluation results are shown in Table 1. Details of each component shown in Table 1 used in these Examples are as follows.
Synthetic oil: poly-α-olefin, kinematic viscosity at 100° C.: 1.8 mm2/s, kinematic viscosity at 40° C.: 5.1 mm2/s, viscosity index: 128.
PMA-A: polymethacrylate having a functional group containing an oxygen atom in the molecule (having a structural unit represented by the general formula (I) where R1 is at least one selected from an alkyl group having 24 to 40 carbon atoms, and X1 is a hydroxy group), mass average molecular weight: 30,000.
PMA-B: polymethacrylate having a functional group containing an oxygen atom in the molecule (having a structural unit represented by the general formula (I) where R1 is at least one selected from an alkyl group having 24 to 40 carbon atoms, and X1 is a hydroxy group), mass average molecular weight: 35,000.
PMA-C: polymethacrylate having a functional group containing an oxygen atom in the molecule (having a structural unit represented by the general formula (I) where R1 is at least one selected from an alkyl group having 24 to 40 carbon atoms, and X1 is a hydroxy group), mass average molecular weight: 50,000.
PMA-D: polymethacrylate not having a functional group containing an oxygen atom in the molecule, mass average molecular weight: 30,000.
PMA-E: polymethacrylate not having a functional group containing an oxygen atom in the molecule, mass average molecular weight: 200,000.
Other additives: phenol-based antioxidant, metal-based detergent (overbased calcium sulfonate), dispersant (boron-free polybutenylsuccinic acid bisimide, boron-containing polybutenylsuccinic acid monoimide), friction modifier (fatty acid amine, fatty acid amide).
The properties of the lubricating oil compositions were measured according to the following methods.
(1) Kinematic Viscosity
The kinematic viscosity at 40° C. and 100° C. was measured according to JIS K 2283:2000.
(2) Viscosity Index (VI)
Measured according to JIS K 2283:2000.
(3) Calculation of Rate of Change in Kinematic Viscosity
With respect to the ultrasonically-treated composition obtained by irradiating a lubricating oil composition with ultrasonic waves for 60 minutes according to JASO M347-95 and an untreated lubricating oil composition, their kinematic viscosity at 40° C. (v1, v0) was measured according to JIS K2283:2000. The rate of reduction ((v0−v1)/v0×100) was calculated, and this is referred to as the rate of change in kinematic viscosity at 40° C. In place of their kinematic viscosity at 40° C., their kinematic viscosity at 100° C. was measured, and the rate of change in kinematic viscosity at 100° C. was calculated.
The lubricating oil compositions of the present embodiment of Examples 1 to 3 all have a high viscosity index of 279, 291 and 304, respectively, and the rate of change in kinematic viscosity at 40° C. thereof was 0.61%, 1.05% and 2.12%, respectively, and was extremely small. Thus, the lubricating oil compositions were confirmed to satisfy both high viscosity index and high shear stability. On the other hand, regarding the lubricating oil composition of Comparative Example 1 using a polymethacrylate not having a functional group containing an oxygen atom, the rate of change in kinematic viscosity at 40° C. thereof was 1.27% and was small, but the viscosity index thereof was 254 and was a lower than the viscosity index the lubricating oil compositions of Examples 1 to 3 have, that is, the comparative composition could not be said to have a high viscosity index. The lubricating oil composition of Comparative Example 2 using a polymethacrylate not having a functional group containing an oxygen atom, whose mass average molecular weight was larger than the mass average molecular weight the polymethacrylate used in Comparative Example 1 has, had a high viscosity index of 318, but the rate of change in kinematic viscosity at 40° C. thereof was 14.1% and was large, that is, the comparative composition could not be said to have high shear stability.
The lubricating oil composition and the lubrication method of the present invention is favorably used for transmissions such as those of gasoline vehicles, hybrid vehicles and electric vehicles. The transmission of the present invention is favorably used as a transmission of gasoline vehicles, hybrid vehicles and electric vehicles.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2016-042504 | Mar 2016 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2017/008255 | 3/2/2017 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2017/150656 | 9/8/2017 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 20070191239 | Matsuoka et al. | Aug 2007 | A1 |
| 20100093576 | Maruyama et al. | Apr 2010 | A1 |
| 20110003725 | Matsui | Jan 2011 | A1 |
| 20110053815 | Matsui et al. | Mar 2011 | A1 |
| 20110124536 | Matsui | May 2011 | A1 |
| 20120108481 | Nagatomi | May 2012 | A1 |
| Number | Date | Country |
|---|---|---|
| 2004-149794 | May 2004 | JP |
| 2006-117854 | May 2006 | JP |
| 2008-133440 | Jun 2008 | JP |
| 2009-167277 | Jul 2009 | JP |
| 2009-179694 | Aug 2009 | JP |
| 2010-285471 | Dec 2010 | JP |
| 2015-172165 | Oct 2015 | JP |
| Entry |
|---|
| International Search Report dated Mar. 28, 2017, in PCT/JP2017/008255, filed Mar. 2, 2017. |
| Japanese Office Action dated Nov. 12, 2019 in Patent Application No. 2016-042504 (with English translation), 4 pages. |
| Number | Date | Country | |
|---|---|---|---|
| 20190112541 A1 | Apr 2019 | US |
