LUBRICATING OIL COMPOSITION

- ENEOS Corporation

A lubricating oil composition including: a lubricant base oil; (A) a calcium salicylate detergent in an amount of 0.005 to 0.03 mass % in terms of calcium on the basis of the total mass of the composition; and (B) a phosphite ester compound represented by the following general formula (1) in an amount of 0.01 to 0.06 mass % in terms of phosphorus on the basis of the total mass of the composition: wherein in the general formula (1), R1 and R2 are each independently a C5-20 group represented by the following general formula (2): wherein in the general formula (2), R3 is a C2-17 linear chain hydrocarbon group, and R4 is a C3-17 linear chain hydrocarbon group, and X1 is an oxygen atom or a sulfur atom.

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Description
FIELD

The present invention relates to a lubricating oil composition, and specifically to a lubricating oil composition suitable for lubrication of electric motors.

BACKGROUND

In recent years, electric vehicles which use an electric motor as a power source for running, and hybrid vehicles which use an electric motor and an internal combustion engine together as a power source for running are attracting interest in view of energy efficiency and environmental compatibility. While generating heat during operation thereof, electric motors include heat-sensitive components such as a coil and a magnet. Those vehicles using an electric motor as a power source for running are thus provided with means for cooling the electric motor. Known means for cooling the electric motor include air cooling, water cooling and oil cooling. Among them, oil cooling is to circulate oil in the electric motor, to directly make parts in the electric motor which generate heat (such as a coil, a core and a magnet) contact with a coolant (oil), which makes it possible to obtain a high cooling effect. In the electric motor using oil cooling, oil (lubricating oil) is circulated in the electric motor, to cool and lubricate the electric motor at the same time. Electrical insulation is required of a lubricating oil (electric motor oil) of the electric motor.

The vehicle using the electric motor as a power source for running usually includes a transmission having a gear mechanism. Various additives are incorporated into a lubricating oil to lubricate the gear mechanism since anti-wear performance and anti-fatigue performance are required of the lubricating oil.

CITATION LIST Patent Literature

  • [Patent Literature 1] JP 2003-113391 A
  • [Patent Literature 2] JP H9-328698 A
  • [Patent Literature 3] JP 2018-053017 A

SUMMARY Technical Problem

A lubricating oil used for lubricating the electric motor is usually different from that used for lubricating the transmission. If the electric motor and the transmission (gear mechanism) can be lubricated using the same lubricating oil, a lubricating oil circulation system can be simplified. Recently, an electric drive module into which the electric motor and the transmission (gear mechanism) are integrated as one device (package) has been also proposed. For lubrication of such an electric drive module, it is desirable to lubricate the electric motor and the transmission (gear mechanism) using the same lubricating oil in view of downsizing and weight reduction.

Disadvantageously, conventional transmission oils suffer insufficient electrical insulation when oxidatively deteriorated by the use thereof even if electrical insulation of fresh oils thereof is improved for the use for lubrication of the electric motor. Anti-wear performance and anti-fatigue performance of conventional electric motor oils are not enough for the use for lubrication of the transmission (gear mechanism).

An object of the present invention is to provide a lubricating oil composition having electrical insulation of the oxidatively deteriorated composition, and anti-wear performance and anti-fatigue performance in a well-balanced manner.

Solution to Problem

The present invention encompasses the following [1] to [15].

[1] A lubricating oil composition comprising:

a lubricant base oil;

(A) a calcium salicylate detergent in an amount of 0.005 to 0.03 mass % in terms of calcium on the basis of the total mass of the composition; and

(B) a phosphite ester compound represented by the following general formula (1) in an amount of 0.01 to 0.06 mass % in terms of phosphorus on the basis of the total mass of the composition:

wherein in the general formula (1), R1 and R2 are each independently a C5-20 group represented by the following general formula (2):

wherein in the general formula (2), R3 is a C2-17 linear chain hydrocarbon group, and R4 is a C3-17 linear chain hydrocarbon group, and X1 is an oxygen atom or a sulfur atom.

[2] The lubricating oil composition according to [1],

wherein a sum (Ca+P) of a calcium content (Ca) and a phosphorus content (P) in the composition is 0.015 to 0.075 mass %.

[3] The lubricating oil composition according to [1] or [2], wherein the composition has a kinematic viscosity at 40° C. of 4 to 20 mm2/s; and

the composition has a kinematic viscosity at 100° C. of 1.8 to 4.0 mm2/s.

[4] The lubricating oil composition according to any one of [1] to [3], further comprising:

(C) a tolyltriazole metal deactivator and/or a benzotriazole metal deactivator, in an amount of 0.001 to 0.1 mass % on the basis of the total mass of the composition.

[5] The lubricating oil composition according to any one of [1] to [4], optionally further comprising:

an amine antioxidant as (D) an antioxidant in an amount of no more than 0.15 mass % in terms of nitrogen on the basis of the total mass of the composition.

[6] The lubricating oil composition according to any one of [1] to [5], optionally comprising: (F) a nitrogen-containing oiliness agent-based friction modifier in an amount of no more than 0.03 mass % in terms of nitrogen on the basis of the total mass of the composition, a content of the component (F) being a total content of any aliphatic amine compound having a C8-36 aliphatic hydrocarbyl group other than a succinimide ashless dispersant and an amine antioxidant, and any compound having a C8-36 aliphatic hydrocarbyl or aliphatic hydrocarbylcarbonyl group and an amide bond other than a succinimide ashless dispersant and an amine antioxidant.

[7] The lubricating oil composition according to any one of [1] to [6],

wherein a total content of any metallic detergent is no more than 0.03 mass % in terms of metal on the basis of the total mass of the composition.

[8] The lubricating oil composition according to any one of [1] to [7],

wherein a proportion of any salicylate in a total soap group content of any metallic detergent is no less than 65 mass %.

[9] The lubricating oil composition according to any one of [1] to [8], wherein a total phosphorus content in the lubricating oil composition is no more than 0.06 mass % in terms of phosphorus on the basis of the total mass of the composition.

[10] The lubricating oil composition according to any one of [1] to [9], wherein a total content of any metal element in the lubricating oil composition is no more than 0.03 mass % in terms of metal on the basis of the total mass of the composition.

[11] The lubricating oil composition according to any one of [1] to [10], wherein a total content of any compound having an O/N-based active hydrogen-containing group is 0 to 500 mass ppm in terms of the sum of oxygen content and nitrogen content on the basis of the total mass of the lubricating oil composition, the compound not contributing to any content of the metallic detergent, a succinimide ashless dispersant, the amine antioxidant, a succinimide friction modifier, a phosphite diester compound that does not have an O/N-based active hydrogen-containing group in its alcohol residue, and a triazole metal deactivator, the O/N-based active hydrogen-containing group representing a non-phenolic OH group that may be part of any other functional group, or a salt thereof, >NH group, or —NH2 group.

[12] The lubricating oil composition according to any one of [1] to [11], wherein an oxidatively deteriorated oil of the composition has a volume resistivity at 80° C. of no less than 1.0×109 Ω·cm, wherein the oxidatively deteriorated oil is obtained by oxidatively treating the composition for 150 hours by ISOT method conforming to JIS K2514-1.

[13] The lubricating oil composition according to any one of [1] to [12], wherein the composition is used to lubricate an electric motor or to lubricate the electric motor and a transmission, in an automobile comprising the electric motor.

[14] A method for lubricating an electric motor, the method comprising: lubricating an electric motor installed in an automobile, by means of the lubricating oil composition as defined in any one of [1] to [13].

[15] A method for lubricating an electric motor and a transmission, the method comprising: lubricating an electric motor and a transmission installed in an automobile, by means of the lubricating oil composition as defined in any one of [1] to [13].

Advantageous Effects

According to the first aspect of the present invention, a lubricating oil composition having electrical insulation of the oxidatively deteriorated composition, and anti-wear performance and anti-fatigue performance in a well-balanced manner can be provided.

The lubricating oil composition according to the first aspect of the present invention may be preferably used in the lubricating method according to the second aspect of the present invention.

DESCRIPTION OF EMBODIMENTS

The present invention will be hereinafter described. In the present description, expression “A to B” concerning numeral values A and B means “no less than A and no more than B” unless otherwise specified. In such expression, if a unit is added only to the numeral value B, the same unit is applied to the numeral value A. Also, a word “or” means a logical sum unless otherwise specified. In the present description, expression “E1 and/or E2” concerning elements E1 and E2 means “E1, or E2, or the combination thereof”, and expression “E1, . . . , EN-1, and/or EN” concerning elements E1, . . . , EN (N is an integer of 3 or more) means “E1, . . . , EN-1, or EN, or any combination thereof”.

<Lubricating Base Oil>

As a lubricating base oil in the lubricating oil composition according to the present invention (hereinafter may be referred to as “lubricating oil composition” or simply “composition”), at least one mineral base oil, at least one synthetic base oil, or any mixed base oil thereof may be used, and in one embodiment, a Group II base oil, a Group III base oil, a Group IV base oil, or a Group V base oil of API base stock categories, or a mixed base oil thereof may be preferably used. An API Group II base oil is a mineral base oil containing no more than 0.03 mass % sulfur and no less than 90 mass % saturates, and having a viscosity index of no less than 80 and less than 120. An API Group III base oil is a mineral base oil containing no more than 0.03 mass % sulfur and no less than 90 mass % saturates, and having a viscosity index of no less than 120. An API Group IV base oil is a poly-α-olefin base oil. An API Group V base oil is a base oil other than the foregoing Groups I to IV base oils, and preferred examples thereof includes ester base oils.

The mineral base oil may be, for example, a paraffinic or naphthenic mineral base oil obtained through application of one or at least two of refining means in suitable combination, such as solvent deasphalting, solvent extraction, hydrocracking, solvent dewaxing, catalytic dewaxing, hydrorefining, sulfuric acid washing, and white clay treatment, to lubricant oil fractions that are obtained by distillation of crude oil under atmospheric pressure and under reduced pressure. API Group II and Group III base oils are usually produced via hydrocracking. A wax isomerized base oil, a base oil produced by a process of isomerizing GTL WAX (gas to liquid wax), or the like may be also used.

Examples of API Group IV base oils include ethylene-propylene copolymers, polybutene, 1-octene oligomers, and 1-decene oligomers, and hydrogenated products thereof.

Examples of API Group V base oils include monoesters (such as butyl stearate, octyl laurate, and 2-ethylhexyl oleate); diesters (such as ditridecyl glutarate, bis(2-ethylhexyl) adipate, diisodecyl adipate, ditridecyl adipate, and bis(2-ethylhexyl) sebacate); polyesters (such as trimellitate esters); and polyol esters (such as trimethylolpropane caprylate, trimethylolpropane pelargonate, pentaerythritol 2-ethylhexanoate, and pentaerythritol pelargonate).

The lubricating base oil (total base oil) may comprise one base oil, or may be a mixed base oil comprising at least two base oils. In the mixed base oil comprising at least two base oils, the API base stock categories of these base oils may be the same, or may be different from each other. The content of the API Group V base oil is preferably 0 to 20 mass %, and more preferably 0 to 15 mass %; and in one embodiment, may be 0 to 10 mass %, on the basis of the total mass of the lubricating base oil. The content of the ester base oil at the above described upper limit or less can improve oxidation stability of the lubricating oil composition.

The kinematic viscosity of the lubricating base oil (total base oil) at 100° C. is preferably 1.7 to 4.0 mm2/s, and more preferably 2.2 to 3.0 mm2/s; and in one embodiment, may be 1.7 to 3.5 mm2/s. The kinematic viscosity of the lubricating base oil at 100° C. at the above described upper limit or less can improve fuel efficiency. The kinematic viscosity of the lubricating base oil at 100° C. at the above described lower limit or more can further improve anti-wear performance, and anti-fatigue performance, and can also improve electrical insulation of a fresh oil. In the present description, “kinematic viscosity at 100° C.” means a kinematic viscosity at 100° C. specified in ASTM D-445.

The kinematic viscosity of the lubricating base oil (total base oil) at 40° C. is preferably 5.0 to 20.0 mm2/s, and more preferably 7.0 to 12.0 mm2/s; and in one embodiment, may be 5.0 to 14.7 mm2/s. The kinematic viscosity of the lubricating base oil at 40° C. at the above described upper limit or less can improve fuel efficiency. The kinematic viscosity of the lubricating base oil at 40° C. at the above described lower limit or more can further improve anti-wear performance and anti-fatigue performance, and can also improve electrical insulation of a fresh oil. In the present description, “kinematic viscosity at 40° C.” means a kinematic viscosity at 40° C. specified in ASTM D-445.

The viscosity index of the lubricating base oil (total base oil) is preferably no less than 100, and more preferably no less than 105; and in one embodiment, may be no less than 110, may be no less than 120, and may be no less than 125. The viscosity index of the lubricating base oil at the above described lower limit or more can improve viscosity-temperature characteristics and thermal and oxidation stability, can reduce a friction coefficient, and can further improve anti-wear performance of the lubricating oil composition. In the present description, a viscosity index means a viscosity index measured conforming to JIS K 2283-1993.

The sulfur content in the lubricating base oil (total base oil) is, in view of oxidation stability, preferably no more than 0.03 mass % (300 mass ppm), more preferably no more than 50 mass ppm, and especially preferably no more than 10 mass ppm, and may be no more than 1 mass ppm.

The lubricating base oil (total base oil) is a major constituent of the lubricating oil composition. The content of the lubricating base oil (total base oil) in the lubricating oil composition is preferably 80 to 98 mass %, and more preferably 83 to 90 mass %; and in one embodiment, may be 83 to 93 mass %, on the basis of the total mass of the composition.

<(A) Calcium Salicylate Detergent>

The lubricating oil composition of the present invention comprises (A) a calcium salicylate detergent (hereinafter may be simply referred to as “component (A)”). As the component (A), a calcium salicylate, or a basic salt or overbased salt thereof may be used. As the component (A), one calcium salicylate detergent may be used alone, or at least two calcium salicylate detergents may be used in combination. Examples of the calcium salicylate include any compound represented by the following general formula (3).

In the general formula (3), R5 each independently represent a C14-30 alkyl or alkenyl group; and a represents 1 or 2, and is preferably 1. The compound represented by the general formula (3) may be a mixture of any compound of the general formula (3) where a=1 and any compound of the general formula (3) where a=2. When a=2, R5 may be any combination of different groups.

One preferred embodiment of the calcium salicylate detergent may be a calcium salicylate represented by the above general formula (3) where a=1, or a basic salt or overbased salt thereof.

The method for producing the calcium salicylate is not particularly restricted, and a known method for producing monoalkylsalicylates or the like may be used. For example, the calcium salicylate may be obtained by: making a calcium base such as oxides and hydroxides of calcium react with a monoalkylsalicylic acid obtained by alkylating a phenol as a starting material with an olefin, and then carboxylating the resultant product with carbonic acid gas or the like, or with a monoalkylsalicylic acid obtained by alkylating a salicylic acid as a starting material with an equivalent of the olefin, or the like; converting the above monoalkylsalicylic acid or the like to an alkali metal salt such as a sodium salt and a potassium salt, and then performing transmetallation with a calcium salt; or the like.

The method for obtaining the overbased calcium salicylate is not particularly restricted. For example, a calcium salicylate is made to react with a calcium base such as calcium hydroxide in the presence of carbonic acid gas, which makes it possible to obtain the overbased calcium salicylate.

The base number of the component (A) is not particularly limited, but is preferably 50 to 350 mgKOH/g, more preferably 100 to 350 mgKOH/g, and especially preferably 150 to 350 mgKOH/g. The base number of the component (A) at the above described lower limit or more can further improve electrical insulation of the oxidatively deteriorated composition.

The content of the component (A) in the lubricating oil composition is 0.005 to 0.03 mass %, and preferably 0.005 to 0.02 mass %, in terms of calcium on the basis of the total mass of the lubricating oil composition. The content of the component (A) at the above described upper limit or less can improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The content of the component (A) at the above described lower limit or more can improve anti-fatigue performance.

The lubricating oil composition may comprise the component (A) only, and may further comprise at least one metallic detergent other than the calcium salicylate detergent (such as a calcium sulfonate detergent and a calcium phenate detergent) in addition to the component (A), as a metallic detergent. The total content of the metallic detergent in the lubricating oil composition is preferably 0.005 to 0.03 mass % in terms of metal on the basis of the total mass of the composition. The total content of the metallic detergent in the lubricating oil composition at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The proportion of total salicylates in the total soap group content of the metallic detergent, that is, the proportion of mass of the total soap group of the salicylate detergent in terms of organic acid to mass of the total soap group of the metallic detergent in terms of organic acid is preferably 65 to 100 mass %, and more preferably 90 to 100 mass %. Contribution of salicylates to the total soap group content of the metallic detergent at the above described lower limit or more can further improve anti-fatigue performance. In the present description, a soap group of the metallic detergent means a conjugate base of an organic acid which constitutes the soap content of the metallic detergent (examples thereof in the salicylate detergent include alkylsalicylate anions, examples thereof in the sulfonate detergent include alkylbenzenesulfonate anions, and examples thereof in the phenate detergent include alkylphenate anions).

<(B) Phosphite Ester Compound>

The lubricating oil composition according to the present invention comprises a phosphite ester compound represented by the general formula (1) (hereinafter may be referred to as “component (B)”). As the component (B), one phosphite ester compound may be used alone, or at least two phosphite ester compounds may be used in combination.

In the general formula (1), R1 and R2 are each independently a C5-20 group represented by the following general formula (2).

In the general formula (2), R3 is a C2-17 linear chain hydrocarbon group, preferably an ethylene group or a propylene group, and in one embodiment, an ethylene group; R4 is a C3-17, preferably a C3-16, and especially preferably a C6-10 linear chain hydrocarbon group. X1 is an oxygen atom or a sulfur atom, preferably a sulfur atom.

Using a phosphite ester compound having the foregoing structure as the component (B) can improve anti-wear performance and anti-fatigue performance, and also makes it possible to suppress deterioration of electrical insulation of a fresh oil and an oxidatively deteriorated oil.

Preferred examples of R1 and R2 include 3-thiahexyl group, 3-thiaheptyl group, 3-thiaoctyl group, 3-thianonyl group, 3-thiadecyl group, 3-thiaundecyl group, 4-thiahexyl group, 3-oxapentyl group, 3-oxahexyl group, 3-oxaheptyl group, 3-oxaoctyl group, 3-oxanonyl group, 3-oxadecyl group, 3-oxaundecyl group, 3-oxadodecyl group, 3-oxatridecyl group, 3-oxatetradecyl group, 3-oxapentadecyl group, 3-oxahexadecyl group, 3-oxaheptadecyl group, 3-oxaheptadecyl group, 3-oxanonadecyl group, 4-oxahexyl group, 4-oxaheptyl group, and 4-oxaoctyl group.

The content of the component (B) in the lubricating oil composition is 0.01 to 0.06 mass %, preferably 0.02 to 0.06 mass %, more preferably 0.02 to 0.05 mass %, and especially preferably 0.02 to 0.04 mass %; and in one embodiment, may be 0.02 to 0.06 mass %, in terms of phosphorus on the basis of the total mass of the composition. The content of the component (B) at the above described upper limit or less can improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The content of the component (B) at the above described lower limit or more can improve anti-wear performance.

<(C) Triazole Metal Deactivator>

In one preferred embodiment, the lubricating oil composition may further comprise a tolyltriazole metal deactivator and/or a benzotriazol metal deactivator (hereinafter may be referred to as “component (C)”). As the component (C), any tolyltriazole metal deactivator and/or benzotriazol metal deactivator used in lubricating oils may be used without particular limitations. As the component (C), one compound may be used alone, or at least two compounds may be used in combination.

The lubricating oil composition may optionally comprise the component (C). When the lubricating oil composition comprises the component (C), the content of the component (C) is preferably 0.001 to 0.1 mass %, more preferably 0.001 to 0.075 mass %, and especially preferably 0.001 to 0.05 mass %. The content of the component (C) at the above described lower limit or more can further improve copper corrosion inhibition performance.

The content of the component (C) at the above described upper limit or less can further improve anti-wear performance, and electrical insulation of a fresh oil and the oxidatively deteriorated composition.

<(D) Succinimide Ashless Dispersant>

In one preferred embodiment, the lubricating oil composition may further comprise (D) a succinimide ashless dispersant (hereinafter may be referred to as “component (D)”). The component (D) may include a boronated succinimide ashless dispersant, may include a non-boronated succinimide ashless dispersant, or may include any combination thereof. In view of oxidation stability, the component (D) preferably includes a boronated succinimide ashless dispersant.

As the component (D), for example, succinimide having at least one alkyl or alkenyl group in its molecule, or any derivative (modified compound) thereof may be used. Examples of succinimide having at least one alkyl or alkenyl group in its molecule include any compound represented by the following general formula (4) or (5).

In the general formula (4), R6 represents a C40-400 alkyl or alkenyl group; and b is an integer of 1 to 5, preferably 2 to 4. The carbon number of R6 is preferably no less than 60, and preferably no more than 350.

In the general formula (5), R7 and R8 each independently represent a C40-400 alkyl or alkenyl group, and may be any combination of different groups; and c is an integer of 0 to 4, preferably 1 to 4, more preferably 1 to 3. The carbon numbers of R7 and R8 are preferably no less than 60, and preferably no more than 350.

The carbon numbers of R6 to R8 in the general formulae (4) and (5) at the above described lower limits or more make it possible to obtain good solubility in the lubricating base oil. In contrast, the carbon numbers of R6 to R8 at the above described upper limits or less can improve low-temperature fluidity of the lubricating oil composition.

The alkyl or alkenyl groups (R6 to R8) in the general formulae (4) and (5) may be linear chain or branched, and preferred examples thereof include branched alkyl groups and branched alkenyl groups derived from oligomers of olefins such as propylene, 1-butene, and isobutene, or from co-oligomers of ethylene and propylene. Among them, a branched alkyl or alkenyl group derived from oligomers of isobutene which are conventionally referred to as polyisobutylene, or a polybutenyl group is most preferable.

Preferred number average molecular weights of the alkyl or alkenyl groups (R6 to R8) in the general formulae (4) and (5) are 800 to 3500, and in one embodiment 1000 to 3500.

Succinimide having at least one alkyl or alkenyl group in its molecule includes so-called monotype succinimide represented by the general formula (4) where only an amino group at one terminal of a polyamine chain is imidated, and so-called bistype succinimide represented by the general formula (5) where amino groups at both terminals of a polyamine chain are imidated. The component (D) may comprise either monotype or bistype succinimide, or may comprise both as a mixture. The content of bistype succinimide or any derivative (modified compound) thereof in the component (D) is preferably no less than 50 mass %, and more preferably no less than 70 mass %, on the basis of the total mass of the component (D) (100 mass %).

The method for producing succinimide having at least one alkyl or alkenyl group in its molecule is not specifically limited. For example, such succinimide may be obtained as a condensation reaction product by: reaction of alkyl- or alkenyl-succinic acid having a C40-400 alkyl or alkenyl group or anhydride thereof, with a polyamine. As the component (D), such a condensation product may be used as it is, or may be converted into a derivative (modified compound) described later to be used. The condensation product of alkyl- or alkenyl-succinic acid or anhydride thereof, and a polyamine may be bistype succinimide where both terminals of a polyamine chain are imidated (see the general formula (5)), may be monotype succinimide where only one terminal of a polyamine chain is imidated (see the general formula (4)), or may be a mixture thereof. Here, an alkenyl-succinic acid anhydride having a C40-400 alkenyl group may be obtained by reaction of a C40-400 alkene and maleic anhydride, and an alkyl-succinic acid anhydride having a C40-400 alkyl group may be obtained by a catalytic hydrogenation reaction of such an alkenyl-succinic acid anhydride. Examples of an alkene to react with maleic anhydride may include oligomers of olefins and co-oligomers of ethylene and propylene as described above, and may include isobutene oligomers. Examples of a polyamine include diethylenetriamine, triethylenetetramine, tetraethylenepentamine, and pentaethylenehexamine, and any mixtures thereof, and a polyamine raw material comprising at least one selected therefrom may be preferably used. The polyamine raw material may further or optionally comprise ethylenediamine. In view of improvement of the performance of the condensation product or derivative (modified compound) thereof as a dispersant, the content of ethylenediamine in the polyamine raw material is preferably 0 to 10 mass %, and more preferably 0 to 5 mass %, on the basis of the total mass of the polyamine raw material. Succinimide obtained as the condensation reaction product of alkyl- or alkenyl-succinic acid having a C40-400 alkyl or alkenyl group or anhydride thereof, and a mixture of at least two polyamines is a mixture of the compounds of the general formula (4) or (5) having different values of b or c.

As the derivative (modified compounds) of succinimide, a boron-modified compound (boronated succinimide) where a part or all of the residual amino and/or imino groups is/are neutralized or amidated by reacting succinimide as described above with boric acid may be preferably used.

The weight average molecular weight of the succinimide ashless dispersant is preferably 1000 to 20000, in one embodiment, 2000 to 20000, and in one embodiment, 4000 to 9000.

The lubricating oil composition may optionally comprise the component (D). When the lubricating oil composition comprises the component (D), the content of the component (D) is preferably 1 to 8 mass %, and in one embodiment, may be 1 to 6 mass %, on the basis of the total mass of the lubricating oil composition. The content of the component (D) at the above described lower limit or more can improve electrical insulation of a fresh oil. The content of the component (D) at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. In view of further improvement of electrical insulation of the oxidatively deteriorated composition, the content of the component (D) in the lubricating oil composition is preferably no more than 0.25 mass % in terms of nitrogen on the basis of the total mass of the lubricating oil composition.

<(E) Antioxidant>

In one preferred embodiment, the lubricating oil composition may further comprise (E) an antioxidant (hereinafter may be referred to as “component (E)”). As the component (E), one antioxidant may be used alone, and at least two antioxidants may be used in combination. As the component (E), any known antioxidant such as a phenolic antioxidant and an amine antioxidant may be used without particular limitation.

Examples of the amine antioxidant include aromatic amine antioxidants and hindered amine antioxidants. Examples of the aromatic amine antioxidant include primary aromatic amine compounds such as phenyl-α-naphthylamine; and secondary aromatic amine compounds such as alkylated diphenylamine, alkylated-α-naphthylamine, alkylated phenyl-α-naphthylamine, and phenyl-β-naphthylamine. As the aromatic amine antioxidant, alkylated diphenylamine, or alkylated phenyl-α-naphthylamine, or the combination thereof may be preferably used. Examples of the hindered amine antioxidant include compounds each having a 2,2,6,6-tetraalkylpiperidine skeleton (2,2,6,6-tetraalkylpiperidine derivatives). There may be no substituent in N-position of the 2,2,6,6-tetraalkylpiperidine skeleton, and an alkyl group may be substituted in N-position thereof. The 2,2,6,6-tetraalkylpiperidine derivative may have a substituent (such as acyloxy group, alkoxy group, alkylamino group, and acylamino group) in 4-position. Two 2,2,6,6-tetraalkylpiperidine skeletons may be bonded with each other via a substituent (such as hydrocarbylene bis(carbonyloxy) group, hydrocarbylene diamino group, and hydrocarbylene bis(carbonylamino) group) in their respective 4-positions. As the amine antioxidant, the aromatic amine antioxidant may be used, the hindered amine antioxidant may be used, or any combination thereof may be used. The aromatic amine antioxidant may be preferably used.

Examples of the phenolic antioxidant include 4,4′-methylenebis(2,6-di-t-butylphenol); 4,4′-bis(2,6-di-tert-butylphenol); 4,4′-bis(2-methyl-6-tert-butylphenol); 2,2′-methylenebis(4-ethyl-6-tert-butylphenol); 2,2′-methylenebis(4-methyl-6-tert-butylphenol); 4,4′-butylidenebis(3-methyl-6-tert-butylphenol); 4,4′-isopropylidenebis(2,6-di-tert-butylphenol); 2,2′-methylenebis(4-methyl-6-nonylphenol); 2,2′-isobutylidenebis(4,6-dimethylphenol); 2,2′-methylenebis(4-methyl-6-cyclohexylphenol); 2,6-di-tert-butyl-4-methylphenol; 2,6-di-tert-butyl-4-ethylphenol; 2,4-dimethyl-6-tert-butylphenol; 2,6-di-tert-butyl-4-(N,N′-dimethylaminomethyl)phenol; 4,4′-thiobis(2-methyl-6-tert-butylphenol); 4,4′-thiobis(3-methyl-6-tert-butylphenol); 2,2′-thiobis(4-methyl-6-tert-butylphenol); bis(3-methyl-4-hydroxy-5-tert-butylbenzyl) sulfide; bis(3,5-di-tert-butyl-4-hydroxybenzyl) sulfide; 2,2′-thiodiethylene bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate]; tridecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate; pentaerythritol tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate]; octyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate; octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate; and 3-methyl-5-tert-butyl-4-hydroxyphenol fatty acid esters. As the component (E), at least one amine antioxidant may be used, at least one phenolic antioxidant may be used, or any combination thereof may be used. In one embodiment, at least one aromatic amine antioxidant or at least one phenolic antioxidant, or any combination thereof may be preferably used.

The lubricating oil composition may optionally comprise the component (E). When the lubricating oil composition comprises the component (E), the content of the component (E) is preferably 0.1 to 1.5 mass %, and more preferably 0.1 to 1.0 mass %, on the basis of the total mass of the lubricating oil composition. The content of the component (E) at the above described lower limit or more can further improve electrical insulation of the oxidatively deteriorated composition. The content of the component (E) at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. In one embodiment, when the lubricating oil composition comprises an amine antioxidant as the component (E), the content of the amine antioxidant is preferably more than 0 mass % and no more than 0.15 mass %, and in one embodiment, may be more than 0 mass % and no more than 0.12 mass %, in terms of nitrogen on the basis of the total mass of the lubricating oil composition. The content of the amine antioxidant at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of the content of the amine antioxidant is not particularly limited, but in one embodiment, may be no less than 0.005 mass % in terms of nitrogen.

When the lubricating oil composition comprises a phenolic antioxidant as the component (E), the content of the phenolic antioxidant is preferably more than 0 mass % and no more than 1.5 mass %, and in one embodiment, may be more than 0 mass % and no more than 1.0 mass %, on the basis of the total mass of the lubricating oil composition. The content of the phenolic antioxidant at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of the content of the phenolic antioxidant is not particularly limited, but in one embodiment, may be no less than 0.1 mass %.

<(F) Nitrogen-Containing Oiliness Agent-Based Friction Modifier>

In one embodiment, the lubricating oil composition may further comprise a nitrogen-containing oiliness agent-based friction modifier (hereinafter may be simply referred to as “component (F)”). Examples of the nitrogen-containing oiliness agent-based friction modifier include a succinimide friction modifier described later, and oiliness agent-based friction modifiers such as amine friction modifiers and amide friction modifiers. The component (F) encompasses aliphatic amine compounds each having a C8-36 aliphatic hydrocarbyl group other than the succinimide ashless dispersant (component (D)) and amine antioxidant (component (E)), and compounds each having a C8-36 aliphatic hydrocarbyl or aliphatic hydrocarbylcarbonyl group and an amide bond other than the succinimide ashless dispersant (component (D)) and amine antioxidant (component (D)).

Examples of the amine friction modifier include aliphatic amine compounds each having a C10-30, preferably a C12-24, more preferably a C12-20 alkyl or alkenyl, preferably linear chain alkyl or linear chain alkenyl group.

Examples of the amide friction modifier include condensation products of a linear or branched chain, preferably linear chain fatty acid, and ammonia, an aliphatic monoamine or an aliphatic polyamine.

One example of the amide friction modifier is a fatty acid amide compound having a C10-30, preferably a C12-24 alkylcarbonyl or alkenylcarbonyl group. For example, such an amide compound can be obtained by a condensation reaction of a C10-30, preferably a C12-24 fatty acid or an acid chloride thereof, and an aliphatic primary or secondary amine compound, an aliphatic primary or secondary alkanolamine compound, or ammonia. The foregoing amine compound and alkanolamine compound each preferably have a C1-30, more preferably a C1-10, further preferably a C1-4 aliphatic group, and in one embodiment have a C1 or C2 aliphatic group.

Examples of the fatty acid amide friction modifier include lauramide, myristamide, palmitamide, stearamide, oleamide, cocamide, and C12-13 synthetic mixed fatty acid amide.

Other examples of the amide friction modifier include fatty acid hydrazides, fatty acid semicarbazides, aliphatic ureas, fatty acid ureides, and aliphatic allophanamides each having a C10-30 alkyl or alkenyl group, or a C10-30 alkylcarbonyl or alkenylcarbonyl group, and derivatives (modified compounds) thereof. Examples of the derivative (modified compound) of the amide friction modifier include boric acid-modified compounds obtained by reacting any amide compound as described above with boric acid or a boric acid salt.

Examples of the aliphatic urea friction modifier include aliphatic urea compounds each having a C12-24, preferably a C12-20 alkyl or alkenyl group such as dodecylurea, tridecylurea, tetradecylurea, pentadecylurea, hexadecylurea, heptadecylurea, octadecylurea, and oleylurea, and acid-modified derivatives thereof (acid-modified compounds such as boric acid-modified compounds).

Examples of the fatty acid hydrazide friction modifier include fatty acid hydrazide compounds each having a C12-24 alkylcarbonyl or alkenylcarbonyl group, such as dodecanoic hydrazide, tridecanoic hydrazide, tetradecanoic hydrazide, pentadecanoic hydrazide, hexadecanoic hydrazide, heptadecanoic hydrazide, octadecanoic hydrazide, oleic hydrazide, erucic hydrazide, and acid-modified derivatives thereof (acid-modified compounds such as boric acid-modified compounds).

Other examples of the amide friction modifier include amide compounds of aliphatic hydroxy acids each having a C1-30 hydroxy-substituted alkyl or alkenyl group. Such an amide compound can be obtained by, for example, a condensation reaction of any aliphatic hydroxy acid as described above with an aliphatic primary or secondary amine compound, or an aliphatic primary or secondary alkanolamine compound. The carbon number of a hydroxy-substituted alkyl or alkenyl group of the above described aliphatic hydroxy acid is preferably 1 to 10, more preferably 1 to 4, and in one embodiment 1 or 2. The aliphatic hydroxy acid is preferably a linear chain aliphatic α-hydroxy acid, and in one embodiment is a glycolic acid. The above described amine compounds and alkanolamine compounds each preferably have a C1-30, more preferably a C10-30, further preferably a C12-24, and especially preferably a C12-20 aliphatic group.

Other examples of the amide friction modifier include amide compounds of a C10-30, preferably a C12-24 fatty acid, and an amino acid (N-acylated amino acid). Examples of the N-acylated amino acid friction modifier include N-acylated-N-methylglycine (such as N-oleoyl-N-methylglycine).

Examples of the succinimide friction modifier include bis-succinimide compounds and mono-succinimide compounds each having a C8-36 alkyl or alkenyl group, and derivatives (modified compounds) thereof. For example, such a succinimide compound is represented by the following general formula (6) or (7).

In the general formulae (6) and (7), R9 and R10 each independently represent a C8-36, preferably a C8-30, more preferably a C12-22, and in one embodiment a C12-18 alkyl or alkenyl group. R11 and R12 each independently represent a C1-4, preferably a C2-3 alkylene group, and especially preferably an ethylene group. R13 is a hydrogen atom or C1-36 alkyl or alkenyl group, preferably a hydrogen atom or C1-30 alkyl or alkenyl group, and preferably a hydrogen atom. d represents an integer of 1-7, preferably 1-4, more preferably 1-3. e represents an integer of 1-7, preferably 1-5, more preferably 2-5, further preferably 2-4.

The method for producing the succinimide friction modifier is not specifically limited. For example, the succinimide compound of the general formula (6) or (7) may be obtained as a condensation reaction product by: reaction of alkyl- or alkenyl-succinic acid having a C8-36, preferably a C8-30, preferably a C12-22 alkyl or alkenyl group or anhydride thereof, with a polyamine, a N-mono-C1-36 alkylated product of the polyamine or a N-mono-C1-36 alkenylated product of the polyamine, or a mixture thereof. As the succinimide friction modifier, such a condensation product may be used as it is, and may be converted into a derivative (modified compound) described later to be used. The condensation product of alkyl- or alkenyl-succinic acid or anhydride thereof, and a polyamine may be bistype succinimide where both terminals of a polyamine chain are imidated (see the general formula (6)), may be monotype succinimide where only one terminal of a polyamine chain is imidated (see the general formula (7)), or may be a mixture thereof. Here, examples of polyamines include diethylenetriamine, triethylenetetramine, tetraethylenepentamine, and pentaethylenehexamine, and any mixtures thereof, and a polyamine raw material comprising at least one selected therefrom may be preferably used. The polyamine raw material may further or optionally comprise ethylenediamine. In view of improvement of the performance of the condensation product or derivative thereof as a friction modifier, the content of ethylenediamine in the polyamine raw material is preferably 0 to 10 mass %, and more preferably 0 to 5 mass %, on the basis of the total mass of the polyamine raw material. As the N-mono-C1-36 alkylated product of the polyamine, a N-mono-C1-36 alkylated polyamine having a C1-36 alkyl group on a nitrogen atom at an end of a chain of the polyamine may be preferably used. As the N-mono-C1-36 alkenylated product of the polyamine, a N-mono-C1-36 alkenylated polyamine having a C1-36 alkenyl group on a nitrogen atom at an end of a chain of the polyamine may be preferably used. In the present description, “Ci-j” (i and j are integers) means that the carbon number is no less than i and no more than j.

Examples of derivatives (modified compounds) of succinimide compounds which may be used as the succinimide friction modifier include modified compounds obtained by reacting any succinimide compound as described above with at least one selected from boric acid, phosphoric acid, a C1-20 carboxylic acid, and a sulfur-containing compound. Among them, a boric acid-modified compound may be preferably used.

The lubricating oil composition may optionally comprise the component (F). The content of the component (F) in the lubricating oil composition is preferably 0 to 0.03 mass %, and in one embodiment, may be 0 to 0.02 mass %, in terms of nitrogen on the basis of the total mass of the composition. The content of the component (F) at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition.

<Other Additives>

In one embodiment, the lubricating oil composition may further comprise at least one additive selected from viscosity index improvers, pour point depressants, anti-wear agents or extreme-pressure agents other than the component (B), friction modifiers other than the component (F), corrosion inhibitors other than the component (C), metal deactivators other than the component (C), anti-rust agents, demulsifiers, anti-foaming agents, and coloring agents.

As the viscosity index improver, any viscosity index improver that is used in lubricating oils may be used without particular limitations. Examples of such a viscosity index improver include polymethacrylates, ethylene-α-olefin copolymers and hydrogenated products thereof, copolymers of an α-olefin and an ester monomer having a polymerizable unsaturated bond, polyisobutylene and hydrogenated products thereof, hydrogenated products of styrene-diene copolymers, styrene-maleic anhydride/ester copolymers, and polyalkylstyrene. Among them, a polymethacrylate, an ethylene-α-olefin copolymer or a hydrogenated product thereof, or any combination thereof may be preferably used. The viscosity index improver may be dispersant type, or may be non-dispersant type. In one embodiment, the weight average molecular weight of the viscosity index improver may be, for example, 2000 to 30000. The lubricating oil composition may optionally comprise the viscosity index improver. When the lubricating oil composition comprises the viscosity index improver, the content of the viscosity index improver is preferably no more than 12 mass %, and more preferably no more than 8 mass %, on the basis of the total mass of the composition. The content of the viscosity index improver at the foregoing upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of this content is not particularly limited, but in one embodiment, may be no less than 1 mass %.

As the pour point depressant, for example, any known pour point depressant such as a polymethacrylate polymer may be used without particular limitations. The lubricating oil composition may optionally comprise the pour point depressant. When the lubricating oil composition comprises the pour point depressant, the content of the pour point depressant in the lubricating oil composition is preferably no more than 1 mass %, and more preferably no more than 0.5 mass %, on the basis of the total mass of the composition. The content of the pour point depressant at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of this content is not particularly restricted, but in one embodiment, may be no less than 0.1 mass %.

Examples of the anti-wear agent or extreme-pressure agent other than component (B) include sulfur-containing compounds such as disulfides, sulfurized olefins, sulfurized oils, and dithiocarbamates, and phosphorus-containing anti-wear agents other than the component (B). Examples of the phosphorus-containing anti-wear agent other than the component (B) include phosphoric acid, thiophosphoric acid, dithiophosphoric acid, trithiophosphoric acid, and complete or partial esters thereof; phosphorous acid, thiophosphoric acid, dithiophosphoric acid, trithiophosphoric acid, monoesters thereof, diesters thereof (excluding diesters represented by the general formula (1)), and triesters thereof. The lubricating oil composition may optionally comprise the anti-wear agent other than the component (B). When the lubricating oil composition comprises the anti-wear agent other than the component (B), the content of this anti-wear agent is preferably no more than 10 mass %, and more preferably no more than 5 mass %, on the basis of the total mass of the composition. The content of this anti-wear agent at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of this content is not particularly limited, but in one embodiment, may be no less than 1 mass %.

The lubricating oil composition may optionally comprise a phosphorus-containing additive other than the component (B). The total phosphorus content in the lubricating oil composition is preferably no more than 0.06 mass % on the basis of the total mass of the composition. The total phosphorus content in the lubricating oil composition at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. In one embodiment, the total content of the phosphorus-containing additive other than the component (B) in the lubricating oil composition is preferably no more than 0.05 mass %, more preferably no more than 0.03 mass %, and further preferably no more than 0.02 mass %, in terms of phosphorus on the basis of the total mass of the composition. The total content of the phosphorus-containing additive other than the component (B) at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition.

As the friction modifier other than the component (F), for example, at least one friction modifier selected from organic molybdenum compounds and oiliness agent-based friction modifiers other than the component (F) may be used. The lubricating oil composition may optionally comprise the friction modifier other than the component (F). When the lubricating oil composition comprises the friction modifier other than the component (F), the total content of this friction modifier is preferably no more than 2 mass %, more preferably no more than 1 mass %, and especially preferably no more than 0.5 mass %, on the basis of the total mass of the composition. The content of this friction modifier at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of this content is not particularly limited, but in one embodiment, may be no less than 0.01 mass %.

Examples of the organic molybdenum compound include sulfur-containing organic molybdenum compounds, and organic molybdenum compounds which do not contain sulfur as a constituent element. Examples of the sulfur-containing organic molybdenum compound include sulfur-containing organic compounds such as molybdenum dithiocarbamate compounds; molybdenum dithiophosphate compounds; complexes of molybdenum compounds (examples thereof include: molybdenum oxides such as molybdenum dioxide and molybdenum trioxide; molybdenum acids such as orthomolybdic acid, paramolybdic acid, and sulfurized (poly)molybdic acid; molybdic acid salts such as metal salts and ammonium salts of these molybdic acids; molybdenum sulfides such as molybdenum disulfide, molybdenum trisulfide, molybdenum pentasulfide, and molybdenum polysulfide; thiomolybdic acid; metal salts and amine salts of thiomolybdic acid; and molybdenum halides such as molybdenum chloride), and sulfur-containing organic compounds (examples thereof include: alkyl (thio)xanthate, thiadiazole, mercaptothiadiazole, thiocarbonate, tetrahydrocarbylthiuram disulfide, bis(di(thio)hydrocarbyl dithiophosphonate) disulfide, organic (poly)sulfide, and sulfurized ester) or other organic compounds; and sulfur-containing organic molybdenum compounds such as complexes of sulfur-containing molybdenum compounds such as the above described molybdenum sulfides and sulfurized molybdic acids, and alkenylsuccinimide. The organic molybdenum compound may be a mononuclear molybdenum compound, or may be a polynuclear molybdenum compound such as binuclear molybdenum compounds and trinuclear molybdenum compounds. Examples of the organic molybdenum compound which does not contain sulfur as a constituent element include molybdenum-amine complexes, molybdenum-succinimide complexes, molybdenum salts of organic acids, and molybdenum salts of alcohols.

The lubricating oil composition may optionally comprise a metal-containing additive other than the metallic detergent (such as organic molybdenum compounds and zinc dialkyl dithiophosphate). The total content of metal elements in the lubricating oil composition is preferably no more than 0.03 mass % in terms of metal on the basis of the total mass of the composition. The total content of metal elements in the lubricating oil composition at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. In one embodiment, the total content of a metal-containing additive other than the metallic detergent in the lubricating oil composition is preferably no more than 0.010 mass %, more preferably no more than 0.0075 mass %, and further preferably no more than 0.0050 mass %, in terms of metal on the basis of the total mass of the composition. The total content of the metal-containing additive other than the metallic detergent at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition.

Examples of the oiliness agent-based friction modifier other than the component (F) include compounds such as fatty acid esters, fatty acids, fatty acid metal salts, aliphatic alcohols, and aliphatic ethers. These compounds each preferably have a C10-30 aliphatic hydrocarbyl or aliphatic hydrocarbylcarbonyl group, more preferably a C10-30 alkyl or alkenyl group or a C10-30 alkylcarbonyl or alkenylcarbonyl group, further preferably a C10-30 linear chain alkyl or linear chain alkenyl group or a C10-30 linear chain alkylcarbonyl or linear chain alkenylcarbonyl group.

As the corrosion inhibitor other than the component (C), for example, any known corrosion inhibitor such as thiadiazole compounds and imidazole compounds may be used without particular limitations. The lubricating oil composition may optionally comprise the corrosion inhibitor other than the component (C). When the lubricating oil composition comprises the corrosion inhibitor other than the component (C), the content of this corrosion inhibitor is preferably no more than 1 mass %, and more preferably no more than 0.5 mass %, on the basis of the total mass of the composition. The content of this corrosion inhibitor at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of the content of this corrosion inhibitor is not particularly restricted, but in one embodiment, may be no less than 0.01 mass %.

As the metal deactivator other than the component (C), for example, any known metal deactivator such as imidazoline, pyrimidine derivatives, alkylthiadiazoles, mercaptobenzothiazoles, 1,3,4-thiadiazole polysulfide, 1,3,4-thiadiazolyl-2,5-bis(dialkyl dithiocarbamate), 2-(alkyldithio)benzimidazole, and β-(o-carboxybenzylthio)propionitrile may be used without particular limitations. The lubricating oil composition may optionally comprise the metal deactivator other than the component (C). When the lubricating oil composition comprises the metal deactivator other than the component (C), the content of this metal deactivator is preferably no more than 1 mass %, and more preferably no more than 0.5 mass %, on the basis of the total mass of the composition. The content of this metal deactivator at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of the content of this metal deactivator is not particularly restricted, but in one embodiment, may be no less than 0.01 mass %.

As the anti-rust agent, for example, any known anti-rust agent such as petroleum sulfonate, alkylbenzenesulfonate, dinonylnaphthalenesulfonate, alkenylsuccinate esters, and polyol esters may be used without particular limitations. The lubricating oil composition may optionally comprise the anti-rust agent. When the lubricating oil composition comprises the anti-rust agent, the content of this anti-rust agent is preferably no more than 1 mass %, and more preferably no more than 0.5 mass %, on the basis of the total mass of the composition. The content of this anti-rust agent at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of the content of this anti-rust agent is not particularly restricted, but in one embodiment, may be no less than 0.01 mass %. In the present description, the content of any metal sulfonate shall contribute to the content of the metallic detergent even when used as the anti-rust agent.

As the demulsifier, for example, any known demulsifier such as polyoxyalkylene glycol-based nonionic surfactants including polyoxyethylene alkyl ether, polyoxyethylene alkylphenyl ether, and polyoxyethylene alkylnaphthyl ether may be used without particular limitations. The lubricating oil composition may optionally comprise the demulsifier. When the lubricating oil composition comprises the demulsifier, the content of this demulsifier is preferably no more than 5 mass %, and more preferably no more than 3 mass %, on the basis of the total mass of the composition. The content of this demulsifier at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of this content is not particularly restricted, but in one embodiment, may be no less than 1 mass %.

As the anti-foaming agent, any known anti-foaming agent such as silicones, fluorosilicones, and fluoroalkyl ethers may be used. The lubricating oil composition may optionally comprise the anti-foaming agent. When the lubricating oil composition comprises the anti-foaming agent, the content of this anti-foaming agent is preferably no more than 0.5 mass %, and more preferably no more than 0.1 mass %, on the basis of the total mass of the composition. The content of this anti-foaming agent at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. The lower limit of this content is not particularly restricted, but in one embodiment, may be no less than 0.0001 mass %.

As the coloring agent, for example, any known coloring agent such as azo compounds may be used.

<Lubricating Oil Composition>

The kinematic viscosity of the lubricating oil composition at 100° C. is preferably 1.8 to 4.0 mm2/s. The kinematic viscosity of the composition at 100° C. at the above described upper limit or less can improve fuel efficiency. The kinematic viscosity of the composition at 100° C. at the above described lower limit or more can further improve anti-seizure performance, anti-wear performance, anti-fatigue performance, and electrical insulation of a fresh oil and the oxidatively deteriorated composition.

The kinematic viscosity of the lubricating oil composition at 40° C. is preferably 4 to 20 mm2/s. The kinematic viscosity of the composition at 40° C. at the above described upper limit or less can improve fuel efficiency. The kinematic viscosity of the composition at 40° C. at the above described lower limit or more can further improve anti-seizure performance, anti-wear performance, anti-fatigue performance, and electrical insulation of a fresh oil and the oxidatively deteriorated composition.

In one embodiment, the sum (Ca+P) of the calcium content (Ca) and the phosphorus content (P) in the lubricating oil composition is preferably 0.015 to 0.075 mass %. This sum Ca+P at the foregoing upper limit or below can further improve electrical insulation of a fresh oil and the oxidatively deteriorated composition. This sum Ca+P at the foregoing lower limit or over can further improve anti-wear performance and anti-fatigue performance.

In one embodiment, the volume resistivity of an oxidatively deteriorated oil of the lubricating oil composition at 80° C. is preferably no less than 1.0×109 Ω·cm. In the present description, the volume resistivity of an oxidatively deteriorated oil is volume resistivity of an oxidatively deteriorated oil measured at 80° C. in oil temperature, conforming to the volume resistivity test specified in JIS C2101: this oxidatively deteriorated oil is obtained by oxidation treatment on a fresh oil at 165° C. for 150 hours by the ISOT method (Indiana Stirring Oxidation Test) specified in JIS K2514-1.

In one embodiment, the total content of any compound having a non-phenolic OH group (which may be part of any other functional group (such as carboxy group and phosphoric acid group)) or a salt thereof, >NH group, or —NH2 group (hereinafter may be referred to as “O/N-based active hydrogen-containing group”), and not contributing to any content of the metallic detergent, the succinimide ashless dispersant, the amine antioxidant, a phosphite diester compound that does not have an O/N-based active hydrogen-containing group in its alcohol residue, and the tolyltriazole metal deactivator is preferably 0 to 500 mass ppm; in one embodiment, may be 0 to 300 mass ppm; and in another embodiment, may be 0 to 150 mass ppm, on the basis of the total mass of the lubricating oil composition in terms of the sum of the oxygen element content and the nitrogen element content. Examples of such an O/N-based active hydrogen compound include phosphoric acid (which may be in a form of a salt) and partial esters thereof; phosphorous acid (which may be in a form of a salt) and partial esters thereof (it is noted that any phosphite diester compound that does not have the above described O/N-based active hydrogen-containing group in its alcohol residue (such as the component (B)) shall not fall under the O/N-based active hydrogen compound); nitrogen-containing oiliness agent-based friction modifiers each having a N—H bond (such as primary fatty amines, secondary fatty amines, fatty acid primary amides, fatty acid secondary amides, aliphatic ureas each having a N—H bond, and fatty acid hydrazides); nitrogen-containing oiliness agent-based friction modifiers each having a hydroxy group (such as amides of fatty acids and primary or secondary alkanolamines, and amides of primary or secondary fatty amines and aliphatic hydroxy acids); nitrogen-containing oiliness agent-based friction modifiers each having a carboxy group (which may be in a form of a salt) (such as N-acylated amino acids); oiliness agent-based friction modifiers each having a hydroxy group (such as glycerol monooleate), and oiliness agent-based friction modifiers each having a carboxy group (which may be in a form of a salt) (such as fatty acids and fatty acid metal salts). When one O/N-based active hydrogen compound comprises both an oxygen element and a nitrogen element, the amounts of both an oxygen element and a nitrogen element derived from this compound shall contribute to the total content of the O/N-based active hydrogen compound (total amount of oxygen and nitrogen elements) irrespective of whether each oxygen atom of the compound is bonded to a hydrogen atom and irrespective of whether each nitrogen atom of the compound is bonded to a hydrogen atom. The total content of the O/N-based active hydrogen compound at the above described upper limit or less can further improve electrical insulation of a fresh oil and the oxidatively deteriorated oil.

(Use)

The lubricating oil composition according to the present invention has balanced electrical insulation of the oxidatively deteriorated composition, anti-wear performance, and anti-fatigue performance, and thus may be preferably used as an electric motor oil, a transmission oil, a common lubricating oil for electric motors and transmissions (gear mechanisms), or a lubricating oil for electric drive modules including an electric motor and a transmission (gear mechanism). In one embodiment, the lubricating oil composition according to the present invention may be preferably used for lubrication of electric motors in automobiles including the electric motor. In another embodiment, the lubricating oil composition according to the present invention may be preferably used for lubrication of electric motors and transmissions (gear mechanism) in automobiles including the electric motor and the transmission (gear mechanism).

EXAMPLES

Hereinafter the present invention will be further specifically described based on examples and comparative examples. The present invention is not limited to these examples.

Examples 1 to 18 and Comparative Examples 1 to 8

As shown in tables 1 to 5, lubricating oil compositions according to the present invention (examples 1 to 18), and lubricating oil compositions for comparison (comparative examples 1 to 8) were each prepared. In the tables, “mass %” for the base oil means mass % on the basis of the total mass of the base oils (the total mass of the base oils is defined as 100 mass %), “mass %” for the other components means mass % on the basis of the total mass of the composition (the total mass of the composition is defined as 100 mass %), and “mass ppm” for the other components means mass ppm on the basis of the total mass of the composition. Details of the components are as follows.

(Lubricating Base Oil)

O-1: hydrorefined mineral oil (Group II, kinematic viscosity (40° C.): 7.7 mm2/s, kinematic viscosity (100° C.): 2.3 mm2/s, viscosity index: 118, sulfur content: less than 1 mass ppm)

O-2: hydrorefined mineral oil (Group III, kinematic viscosity (40° C.): 19.5 mm2/s, kinematic viscosity (100° C.): 4.2 mm2/s, viscosity index: 125, sulfur content: less than 1 mass ppm)

O-3: wax isomerized base oil (Group III, kinematic viscosity (40° C.): 9.3 mm2/s, kinematic viscosity (100° C.): 2.7 mm2/s, viscosity index: 125, sulfur content: less than 1 mass ppm)

O-4: wax isomerized base oil (Group III, kinematic viscosity (40° C.): 15.7 mm2/s, kinematic viscosity (100° C.): 3.8 mm2/s, viscosity index: 143, sulfur content: less than 1 mass ppm)

O-5: poly-α-olefin (Group IV, kinematic viscosity (40° C.): 5.0 mm2/s, kinematic viscosity (100° C.): 1.7 mm2/s)

O-6: poly-α-olefin (Group IV, kinematic viscosity (40° C.): 18.4 mm2/s, kinematic viscosity (100° C.): 4.1 mm2/s, viscosity index: 124)

O-7: monoester base oil (Group V, kinematic viscosity (40° C.): 8.5 mm2/s, kinematic viscosity (100° C.): 2.7 mm2/s, viscosity index: 177)

((A) Calcium detergent)

A-1: calcium salicylate detergent, base number: 325 mgKOH/g

A-2′: calcium sulfonate detergent, base number: 300 mgKOH/g

((B) Phosphite ester)

B-1: bis(3-thiaundecyl) hydrogen phosphite

B-2′: diphenyl hydrogen phosphite

B-3′: dibutyl hydrogen phosphite

B-4′: bis(2-ethylhexyl) hydrogen phosphite

((C) Triazole metal deactivator)

C-1: tolyltriazole metal deactivator

((D) Succinimide ashless dispersant)

D-1: boronated succinimide ashless dispersant

((E) Antioxidant)

E-1: amine antioxidant

E-2: phenolic antioxidant

TABLE 1 examples 1 2 3 4 5 6 base oil composition O-1 mass % 85 60 — — — 75 O-2 mass % 15 — 50 — — 15 O-3 mass % — 40 — — — — O-4 mass % — — — 55 — — O-5 mass % — — 50 45 50 — O-6 mass % — — — — 50 — O-7 mass % — — — — — 10 kinematic viscosity of base oil 40° C. mm2/s 8.7 8.6 9.1 8.9 8.9 8.8 100° C. mm2/s 2.5 2.5 2.5 2.5 2.5 2.5 (A) Ca detergent A-1 mass % (Ca) 0.015 0.015 0.015 0.015 0.015 0.015 A-2* mass % (Ca) — — — — — — (B) phosphite ester B-1 mass % (P) 0.035 0.035 0.035 0.035 0.035 0.035 B-2* mass % (P) — — — — — — B-3* mass % (P) — — — — — — B-4* mass % (P) — — — — — — (C) metal deactivator C-1 mass % 0.05 0.05 0.05 0.05 0.05 0.05 (D) ashless dispersant D-1 mass % 5 5 5 5 5 5 (E) antioxidant E-1 mass % 0.5 0.5 0.5 0.5 0.5 0.5 E-2 mass % 0.5 0.5 0.5 0.5 0.5 0.5 Ca + P mass % 0.050 0.050 0.050 0.050 0.050 0.050 kinematic viscosity of composition 40° C mm2/s 9.7 9.1 10.5 10.1 10.2 9.6 100° C. mm2/s 2.7 2.6 2.8 2.8 2.8 2.7 viscosity index 131 121 114 125 116 116 volume resistivity (80° C.) fresh oil 1010Ω · cm 0.34 0.34 0.34 0.34 0.34 0.35 oxidatively deteriorated oil 1010Ω · cm 0.21 0.21 0.21 0.21 00.21 0.20 high-speed four-ball test size of wear mark mm 0.50 0.50 0.50 0.50 0.50 0.50 unisteel test fatigue life L50 h 20 20 20 20 20 20

TABLE 2 examples 7 8 9 10 11 12 base oil composition O-1 mass % — 50 27 85 85 85 O-2 mass % — 50 73 15 15 15 O-3 mass % — — — — — — O-4 mass % — — — — — — O-5 mass % 100 — — — — — O-6 mass % — — — — — — O-7 mass % — — — — — — kinematic viscosity of base oil 40° C. mm2/s 5.0 11.8 14.7 8.7 8.7 8.7 100° C. mm2/s 1.7 3.0 3.5 2.5 2.5 2.5 (A) Ca detergent A-1 mass % (Ca) 0.015 0.015 0.015 0.005 0.01 0.03 A-2* mass % (Ca) — — — — — — (B) phosphite ester B-1 mass % (P) 0.035 0.035 0.035 0.035 0.035 0.035 B-2* mass % (P) — — — — — — B-3* mass % (P) — — — — — — B-4* mass % (P) — — — — — — (C) metal deactivator C-1 mass % 0.05 0.05 0.05 0.05 0.05 0.05 (D) ashless dispersant D-1 mass % 5 5 5 5 5 5 (E) antioxidant E-1 mass % 0.5 0.5 0.5 0.5 0.5 0.5 E-2 mass % 0.5 0.5 0.5 0.5 0.5 0.5 Ca + P mass % 0.050 0.050 0.050 0.040 0.045 0.065 kinematic viscosity of composition 40° C mm2/s 5.7 13.1 16.1 9.7 9.7 9.7 100° C. mm2/s 1.9 3.3 3.8 2.7 2.7 2.7 viscosity index 114 124 126 131 131 131 volume resistivity (80° C.) fresh oil 1010Ω · cm 0.27 0.40 0.45 0.40 0.36 0.28 oxidatively deteriorated oil 1010Ω · cm 0.15 0.27 0.31 0.23 0.22 0.20 high-speed four-ball test size of wear mark mm unisteel test 0.55 0.48 0.48 0.51 0.50 0.52 fatigue life L50 h 18 21 21 20 20 20

TABLE 3 examples 13 14 15 16 17 18 base oil composition O-1 mass % 85 85 85 85 85 85 O-2 mass % 15 15 15 15 15 15 O-3 mass % — — — — — — O-4 mass % — — — — — — O-5 mass % — — — — — — O-6 mass % — — — — — — O-7 mass % — — — — — — kinematic viscosity of base oil 40° C. mm2/s 8.7 8.7 8.7 8.7 8.7 8.7 100° C. mm2/s 2.5 2.5 2.5 2.5 2.5 2.5 (A) Ca detergent A-1 mass % (Ca) 0.015 0.015 0.015 0.015 0.015 0.015 A-2* mass % (Ca) — — — — — — (B) phosphite ester B-1 mass % (P) 0.02 0.05 0.06 0.035 0.035 0.035 B-2* mass % (P) — — — — — — B-3* mass % (P) — — — — — — B-4* mass % (P) — — — — — — (C) metal deactivator C-1 mass % 0.05 0.05 0.05 — 0.05 0.05 (D) ashless dispersant D-1 mass % 5 5 5 5 5 — (E) antioxidant E-1 mass % 0.5 0.5 0.5 0.5 — 0.5 E-2 mass % 0.5 0.5 0.5 0.5 — 0.5 Ca + P mass % 0.035 0.065 0.075 0.050 0.050 0.050 kinematic viscosity of composition 40° C mm2/s 9.7 9.7 9.7 9.7 9.7 9.5 100° C. mm2/s 2.7 2.7 2.7 2.7 2.7 2.7 viscosity index 131 131 131 131 131 116 volume resistivity (80° C.) fresh oil 1010Ω · cm 0.38 0.25 0.20 0.34 0.35 0.32 oxidatively deteriorated oil 1010Ω · cm 0.25 0.15 0.11 0.21 0.13 0.23 high-speed four-ball test size of wear mark mm 0.52 0.48 0.48 0.49 0.47 0.48 unisteel test fatigue life L50 h 20 20 20 20 21 20

TABLE 4 comparative examples 1 2 3 4 base oil composition O-1 mass % 85 85 85 85 O-2 mass % 15 15 15 15 O-3 mass % — — — — O-4 mass % — — — — O-5 mass % — — — — O-6 mass % — — — — O-7 mass % — — — — kinematic viscosity of base oil 40° C. mm2/s 8.7 8.7 8.7 8.7 100° C. mm2/s 2.5 2.5 2.5 2.5 (A) Ca detergent A-1 mass % (Ca) — — 0.015 0.015 A-2* mass % (Ca) 0.015 0.03 — — (B) phosphite ester B-1 mass % (P) 0.035 0.035 — — B-2* mass % (P) — — 0.035 0.06 B-3* mass % (P) — — — — B-4* mass % (P) — — — — (C) metal deactivator C-1 mass % 0.05 0.05 0.05 0.05 (D) ashless dispersant D-1 mass % 5 5 5 5 (E) antioxidant E-1 mass % 0.5 0.5 0.5 0.5 E-2 mass % 0.5 0.5 0.5 0.5 Ca + P mass % 0.050 0.065 0.050 0.075 kinematic viscosity of composition 40° C. mm2/s 9.7 9.7 9.7 9.7 100° C. mm2/s 2.7 2.7 2.7 2.7 viscosity index 131 131 131 131 volume resistivity (80° C.) fresh oil 1010Ω · cm 0.34 0.28 0.30 0.20 oxidatively deteriorated oil 1010Ω · cm 0.22 0.22 0.15 0.10 high-speed four-ball test size of wear mark mm 0.50 0.51 0.75 0.86 unisteel test fatigue life L50 h 10 9 20 20

TABLE 5 comparative examples 5 6 7 8 base oil composition O-1 mass % 85 85 85 85 O-2 mass % 15 15 15 15 O-3 mass % — — — — O-4 mass % — — — — O-5 mass % — — — — O-6 mass % — — — — O-7 mass % — — — — kinematic viscosity of base oil 40° C. mm2/s 8.7 8.7 8.7 8.7 100° C. mm2/s 2.5 2.5 2.5 2.5 (A) Ca detergent A-1 mass % (Ca) 0.015 0.015 0.035 0.015 A-2* mass % (Ca) — — — — (B) phosphite ester B-1 mass % (P) — — 0.035 0.065 B-2* mass % (P) — — — B-3* mass % (P) 0.035 — — — B-4* mass % (P) — 0.035 — — (C) metal deactivator C-1 mass % 0.05 0.05 0.05 0.05 (D) ashless dispersant D-1 mass % 5 5 5 5 (E) antioxidant E-1 mass % 0.5 0.5 0.5 0.5 E-2 mass % 0.5 0.5 0.5 0.5 Ca + P mass % 0.015 0.050 0.070 0.080 kinematic viscosity of composition 40° C. mm2/s 9.7 9.7 9.7 9.7 100° C. mm2/s 2.7 2.7 2.7 2.7 viscosity index 131 131 131 131 volume resistivity (80° C.) fresh oil 1010Ω · cm 0.19 0.17 0.18 0.10 oxidatively deteriorated oil 1010Ω · cm 0.09 0.08 0.05 0.015 high-speed four-ball test size of wear mark mm 0.70 0.73 0.48 0.48 unisteel test fatigue life L50 h 11 12 21 20

(Volume Resistivity)

The volume resistivity of a fresh oil, and the volume resistivity of an oxidatively deteriorated oil were measured for each lubricating oil composition. The oxidatively deteriorated oil was obtained by oxidation treatment on the fresh oil at 165° C. in oil temperature for 150 hours by the ISOT (Indiana Stirring Oxidation Test) method, conforming to JIS K2514-1. The volume resistivity of the fresh oil, and the volume resistivity of the oxidatively deteriorated oil were each measured at 80° C. in oil temperature, conforming to the volume resistivity test specified in JIS C2101. The results are shown in tables 1 to 5. In this test, higher volume resistivity at 80° C. means better electrical insulation. The volume resistivity of the oxidatively deteriorated oil at 80° C. in this test is preferably no less than 1.0×109 Ω·cm.

(High-Speed Four-Ball Test)

Anti-wear performance of each of the lubricating oil compositions was evaluated by a high-speed four-ball test conforming to JPI-5S-40-93: the size of a wear mark after driving at 1800 rpm in rotation speed at 392 N in load and 80° C. in oil temperature for 30 minutes was measured. The results are shown in tables 1 to 5. In this test, a smaller size of a wear mark means better anti-wear performance.

(Unisteel Test)

For each lubricating oil composition, a rolling fatigue life of a thrust bearing was measured by a Unisteel test (IP305/79, The Institute of Petroleum) using a Unisteel rolling fatigue testing machine (triple-type high-temperature rolling fatigue testing machine (TRF-1000/3-01H) manufactured by Tokyo Koki Testing Machine Co. Ltd.). Time until either a roller or a test piece suffered fatigue damage was measured for a test bearing made by replacing a bearing ring in one side of a thrust needle bearing (FNTA-2542C manufactured by NSK Ltd.) with a flat test piece (material: SUJ2), under the conditions of: 7000 N in load; 2 GPa in surface pressure; 1450 rpm in rotation speed; and 120° C. in oil temperature. It was determined that fatigue damage occurred when the vibration acceleration of a testing portion measured by a vibration accelerometer installed in the Unisteel rolling fatigue testing machine reached 1.5 m/s2. The test was repeated ten times, and then a fatigue life was calculated as the 50% life (L50: time for the cumulative probability to be 50%) by a Weibull plot based on the time it had taken for fatigue damage to occur in the tests. The results are shown in tables 1 to 5. A longer 50% life measured in this test means better anti-fatigue performance.

(Evaluation Results)

The lubricating oil compositions of examples 1 to 18 showed good results in electrical insulation of the oxidatively deteriorated composition, anti-wear performance, and anti-fatigue performance.

The lubricating oil compositions of comparative examples 1 and 2, which comprised a calcium sulfonate detergent instead of the component (A) (calcium salicylate detergent), showed results inferior in anti-fatigue performance.

The lubricating oil compositions of comparative examples 3 to 6, which comprised a phosphite ester compound having a side chain that did not meet the requirements for the component (B), instead of the component (B), showed results inferior in anti-wear performance. Particularly, the lubricating oil compositions of comparative examples 5 and 6, which comprised dialkyl hydrogen phosphite as a phosphite ester compound, showed results inferior in electrical insulation of the fresh oil and the oxidatively deteriorated composition, and anti-fatigue performance as well.

The lubricating oil composition of comparative example 7, which comprised too high a content of the component (A), showed results inferior in electrical insulation of the fresh oil and the oxidatively deteriorated composition.

The lubricating oil composition of comparative example 8, which comprised too high a content of the component (B), showed results inferior in electrical insulation of the fresh oil and the oxidatively deteriorated composition.

Claims

1. A lubricating oil composition comprising: wherein in the general formula (1), R1 and R2 are each independently a C5-20 group represented by the following general formula (2): wherein in the general formula (2), R3 is a C2-17 linear chain hydrocarbon group, and R4 is a C3-17 linear chain hydrocarbon group, and X1 is an oxygen atom or a sulfur atom.

a lubricant base oil;
(A) a calcium salicylate detergent in an amount of 0.005 to 0.03 mass % in terms of calcium on the basis of the total mass of the composition; and
(B) a phosphite ester compound represented by the following general formula (1) in an amount of 0.01 to 0.06 mass % in terms of phosphorus on the basis of the total mass of the composition:

2. The lubricating oil composition according to claim 1,

wherein a sum (Ca+P) of a calcium content (Ca) and a phosphorus content (P) in the composition is 0.015 to 0.075 mass %.

3. The lubricating oil composition according to claim 1,

wherein the composition has a kinematic viscosity at 40° C. of 4 to 20 mm2/s; and
the composition has a kinematic viscosity at 100° C. of 1.8 to 4.0 mm2/s.

4. The lubricating oil composition according to claim 1, further comprising:

(C) a tolyltriazole metal deactivator and/or a benzotriazole metal deactivator, in an amount of 0.001 to 0.1 mass % on the basis of the total mass of the composition.

5. The lubricating oil composition according to claim 1,

wherein an oxidatively deteriorated oil of the composition has a volume resistivity at 80° C. of no less than 1.0×109 Ω·cm, wherein the oxidatively deteriorated oil is obtained by oxidatively treating the composition for 150 hours by ISOT method conforming to JIS K2514-1.

6. The lubricating oil composition according to claim 1,

wherein the composition is used to lubricate an electric motor or to lubricate the electric motor and a transmission, in an automobile comprising the electric motor.

7. A method for lubricating an electric motor, the method comprising:

lubricating an electric motor installed in an automobile, by means of the lubricating oil composition as defined in claim 1.

8. A method for lubricating an electric motor and a transmission, the method comprising:

lubricating an electric motor and a transmission installed in an automobile, by means of the lubricating oil composition as defined in claim 1.
Patent History
Publication number: 20210395635
Type: Application
Filed: Nov 6, 2019
Publication Date: Dec 23, 2021
Applicant: ENEOS Corporation (Tokyo)
Inventors: Yohei SUSUKIDA (Tokyo), Yasushi ONUMATA (Tokyo), Akira TADA (Tokyo)
Application Number: 17/289,993
Classifications
International Classification: C10M 141/10 (20060101); C10M 169/04 (20060101); C10M 129/54 (20060101); C10M 137/02 (20060101); C10M 133/44 (20060101);