LUBRICANT COMPOSITION FOR GEAR OIL

03-09-2020 дата публикации
Номер:
US20200277540A1
Принадлежит: DAELIM INDUSTRIAL CO., LTD.
Контакты:
Номер заявки: 18-08-1668
Дата заявки: 12-11-2019

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001]

This application is based on and claims priority from Korean Patent Application No. 10-2019-0023683, filed on Feb. 28, 2019 with the Korean Intellectual Property Office, the disclosure of which is incorporated herein in its entirety by reference.

BACKGROUND OF THE INVENTION

1. Technical Field

[0002]

The present invention relates to a lubricant composition, and more particularly to a lubricant composition, which includes an ethylene-alphaolefin oligomer and an alkylated phosphonium compound, thus realizing energy reduction and an increased endurance life, and which is thus suitable for use in gear oil.

2. Description of the Related Art

[0003]

Recently, as environmental problems such as global warming, destruction of the ozone layer, etc. have come to the fore, environmental regulations have become strict. Hence, reduction of carbon dioxide emissions is receiving a great deal of attention. In order to reduce carbon dioxide emissions, it is urgent to decrease energy consumption in vehicles, construction machinery, agricultural machinery and the like, that is, to increase fuel economy, and thus there is a strong demand for measures capable of contributing to energy reduction in an engine, a transmission, a final reducer, a compressor, a hydraulic device and the like. Accordingly, lubricants used in such devices are required to have the ability to decrease stirring resistance or friction resistance compared to conventional cases.

[0004]

A lubricant is an oily material used to reduce the generation of frictional force on the friction surface of a machine or to dissipate frictional heat generated from the friction surface. The lubricant is manufactured by adding additives to base oil, and is largely classified into a mineral-oil-based lubricant (petroleum-based lubricant) and a synthetic lubricant depending on the type of base oil, the synthetic lubricant being classified into a polyalphaolefin-based lubricant and an ester-based lubricant.

[0005]

As means for improving fuel economy in gears of transmissions and reducers, decreasing the viscosity of a lubricant is generally used. For example, among transmissions, an automatic transmission or a continuously variable transmission for vehicles has a torque converter, a wet clutch, a gear bearing mechanism, an oil pump, a hydraulic control mechanism, etc., and a manual transmission or a reducer has a gear bearing mechanism, and thus when the viscosity of lubricant used therefor is further decreased, stirring resistance and friction resistance of the torque converter, the wet clutch, the gear bearing mechanism, and the oil pump are decreased, thereby increasing power transmission efficiency, ultimately making it possible to improve the fuel economy of vehicles.

[0006]

However, when the viscosity of conventional lubricants is lowered, fitting performance is greatly decreased due to the deterioration of friction performance, and sticking or the like occurs, thus causing defects in the transmission or the like. Particularly, in the case of low viscosity, a viscosity modifier is sheared during the use thereof, and thus the viscosity is lowered, so that the wear resistance of the gear is damaged and fitting performance is easily deteriorated. Furthermore, even when a sulfur/phosphorus extreme pressure agent is added to increase the extreme pressure performance of low-viscosity oil, fitting performance and endurance life are remarkably decreased, making it difficult to realize long-term use thereof.

[0007]

Therefore, the present inventors have developed a lubricant composition for gear oil, which is capable of reducing the mechanical wear of gear parts and energy consumption and also of exhibiting superior thermal stability and oxidation stability, and may thus be industrially used for a long period of time.

CITATION LIST

Patent Literature

[0008]

(Patent Document 0001) Korean Patent No. 10-1420890

[0009]

(Patent Document 0002) Korean Patent No. 10-1347964

SUMMARY OF THE INVENTION

[0010]

Accordingly, the present invention has been made keeping in mind the problems encountered in the related art, and an objective of the present invention is to provide a lubricant composition, in which a functional additive for friction reduction and an ethylene-alphaolefin liquid random copolymer are mixed, thereby exhibiting superior friction characteristics, thermal stability and oxidation stability.

[0011]

Another objective of the present invention is to provide a lubricant composition for gear oil, which is able to reduce the mechanical wear of gear parts and energy consumption when applied to gears of transmissions and reducers, and may be used for a long period of time due to low changes in the physical properties of gear oil.

[0012]

In order to accomplish the above objectives, the present invention provides a lubricant composition, comprising a base oil, a liquid olefin copolymer, and an alkylated phosphonium compound.

[0013]

The base oil may be at least one selected from the group consisting of mineral oil, polyalphaolefin (PAO) and ester.

[0014]

The liquid olefin copolymer may be prepared by copolymerizing ethylene and alphaolefin in the presence of a single-site catalyst system, and the single-site catalyst system preferably includes a metallocene catalyst, an organometallic compound and an ionic compound.

[0015]

The liquid olefin copolymer may have a coefficient of thermal expansion of 3.0 to 4.0.

[0016]

In the lubricant composition of the present invention, the liquid olefin copolymer may be included in an amount of 0.1 to 30 wt %, and preferably 0.5 to 25 wt %. The alkylated phosphonium compound may be included in an amount of 0.1 to 5.0 wt %, and preferably 0.3 to 4.0 wt %.

[0017]

The lubricant composition may have an SRV friction coefficient of 0.2 to 0.3 and a traction coefficient of 0.15 to 0.3. Moreover, the lubricant composition may have a pinion torque loss rate due to friction of less than 1% in an FZG gear efficiency test.

[0018]

According to the present invention, a lubricant composition includes an alkylated phosphonium compound as a friction-reducing agent, in addition to an existing sulfur/phosphorus extreme pressure agent, thereby maximizing friction performance to thus reduce the mechanical wear of gear parts and energy consumption when applied to gears of transmissions and reducers, ultimately maximizing energy-saving effects.

[0019]

Also, according to the present invention, the lubricant composition includes, as a viscosity modifier, an olefin copolymer prepared in the presence of a metallocene compound catalyst, and can thus exhibit a high viscosity index and superior low-temperature stability.

[0020]

Therefore, the present invention can provide a lubricant composition for gear oil, which enables long-term use due to low changes in the physical properties of gear oil.

DESCRIPTION OF SPECIFIC EMBODIMENTS

[0021]

Hereinafter, a detailed description will be given of the present invention.

[0022]

The present invention relates to a lubricant composition, which has superior oxidation stability and friction characteristics and is thus suitable for use in gear oil. Hence, the lubricant composition of the present invention includes a base oil, a liquid olefin copolymer, and an alkylated phosphonium compound.

[0023]

Here, the base oil varies from the aspects of viscosity, heat resistance, oxidation stability and the like depending on the manufacturing method or refining method, but is generally classified into mineral oil and synthetic oil. The API (American Petroleum Institute) classifies base oil into five types, namely Group I, II, III, IV and V. These types, based on API ranges, are defined in API Publication 1509, 15thEdition, Appendix E, April 2002, and are shown in Table 1 below.

[0000]

Group I<90>0.0380 ≤ VI < 120
Group II≥90≤0.0380 ≤ VI < 120
Group III≥90≤0.03VI ≥ 120
Group IVPAO (Poly Alpha Olefin)
Group VEster & Others

[0024]

In the lubricant composition of the present invention, the base oil may be at least one selected from the group consisting of mineral oil, polyalphaolefin (PAO) and ester, and may be any type among Groups I to V based on the API ranges.

[0025]

More specifically, mineral oil belongs to Groups I to III based on the API ranges, and mineral oil may include oil resulting from subjecting a lubricant distillate fraction, obtained through atmospheric distillation and/or vacuum distillation of crude oil, to at least one refining process of solvent deasphalting, solvent extraction, hydrogenolysis, solvent dewaxing, catalytic dewaxing, hydrorefining, sulfuric acid cleaning, and white clay treatment; wax isomerized mineral oil; or a gas-to-liquid (GLT) oil obtained via the Fischer-Tropsch process.

[0026]

The synthetic oil belongs to Group IV or V based on the API ranges, and polyalphaolefin belonging to Group IV may be obtained through oligomerization of a higher alphaolefin using an acid catalyst, as disclosed in U.S. Pat. No. 3,780,128, 4,032,591, Japanese Patent Application Publication No. Hei. 1-163136, and the like, but the present invention is not limited thereto.

[0027]

Examples of the synthetic oil belonging to Group V include alkyl benzenes, alkyl naphthalenes, isobutene oligomers or hydrides thereof, paraffins, polyoxy alkylene glycol, dialkyl diphenyl ether, polyphenyl ether, ester, and the like.

[0028]

Here, the alkyl benzenes and alkyl naphthalenes are usually dialkylbenzene or dialkylnaphthalene having an alkyl chain length of 6 to 14 carbon atoms, and the alkyl benzenes or alkyl naphthalenes are prepared through Friedel-Crafts alkylation of benzene or naphthalene with olefin. The alkylated olefin used in the preparation of alkyl benzenes or alkyl naphthalenes may be linear or branched olefins or combinations thereof.

[0029]

Also, examples of the ester include, but are not limited to, ditridecyl glutarate, di-2-ethylhexyl adipate, diisodecyl adipate, ditridecyl adipate, di-2-ethylhexyl sebacate, tridecyl pelargonate, di-2-ethylhexyl adipate, di-2-ethylhexyl azelate, trimethylolpropane caprylate, trimethylolpropane pelargonate, trimethylolpropane triheptanoate, pentaerythritol 2-ethylhexanoate, pentaerythritol pelargonate, pentaerythritol tetraheptanoate, and the like.

[0030]

In the lubricant composition of the present invention, the liquid olefin copolymer is prepared by copolymerizing ethylene and alphaolefin monomers in the presence of a single-site catalyst system in order to uniformly distribute alphaolefin units in the copolymer chain. Preferably, the liquid olefin copolymer is prepared by reacting ethylene and alphaolefin monomers in the presence of a single-site catalyst system including a crosslinked metallocene compound, an organometallic compound, and an ionic compound for forming an ion pair through reaction with the crosslinked metallocene compound.

[0031]

Here, the metallocene compound included in the single-site catalyst system may be at least one selected from the group consisting of Chemical Formulas 1 to 6 below.

[0000]

[0032]

In Chemical Formulas 1 to 4,

    • M is a transition metal selected from the group consisting of titanium, zirconium, and hafnium,
    • B is absent or is a linking group including a C1-C20 alkylene group, a C6-C20 arylene group, C1-C20 dialkyl silicon, C1-C20 dialkyl germanium, a C1-C20 alkylphosphine group or a C1-C20 alkylamine group,
    • X1and X2, which are the same as or different from each other, are each independently a halogen atom, a C1-C20 alkyl group, a C2-C20 alkenyl group, a C2-C20 alkynyl group, a C6-C20 aryl group, a C7-C40 alkylaryl group, a C7-C40 arylalkyl group, a C1-C20 alkylamido group, a C6-C20 arylamido group, a C1-C20 alkylidene group or a C1-C20 alkoxy group, and
    • R1to R10, which are the same as or different from each other, are each independently hydrogen, a C1-C20 alkyl group, a C2-C20 alkenyl group, a C6-C20 aryl group, a C7-C20 alkylaryl group, a C7-C20 arylalkyl group, a C5-C60 cycloalkyl group, a C4-C20 heterocyclic group, a C1-C20 alkynyl group, a C6-C20-aryl-containing hetero group or a silyl group.

[0000]

[0037]

In Chemical Formulas 5 and 6,

    • M is a transition metal selected from the group consisting of titanium, zirconium, and hafnium,
    • B is absent or is a linking group including a C1-C20 alkylene group, a C6-C20 arylene group, a C1-C20 dialkyl silicon, a C1-C20 dialkyl germanium, a C1-C20 alkylphosphine group or a C1-C20 alkylamine group,
    • X1and X2, which are the same as or different from each other, are each independently a halogen atom, a C1-C20 alkyl group, a C2-C20 alkenyl group, a C2-C20 alkynyl group, a C6-C20 aryl group, a C7-C40 alkylaryl group, a C7-C40 arylalkyl group, a C1-C20 alkylamido group, a C6-C20 arylamido group, a C1-C20 alkylidene group or a C1-C20 alkoxy group, and
    • R1to R10, which are the same as or different from each other, are each independently hydrogen, a C1-C20 alkyl group, a C2-C20 alkenyl group, a C6-C20 aryl group, a C7-C20 alkylaryl group, a C7-C20 arylalkyl group, a C5-C60 cycloalkyl group, a C4-C20 heterocyclic group, a C1-C20 alkynyl group, a C6-C20-aryl-containing hetero group or a silyl group.

[0042]

Furthermore, all of R11, R13and R14are hydrogen, and each of R12radicals, which are the same as or different from each other, may independently be hydrogen, a C1-C20 alkyl group, a C2-C20 alkenyl group, a C6-C20 aryl group, a C7-C20 alkylaryl group, a C7-C20 arylalkyl group, a C5-C60 cycloalkyl group, a C4-C20 heterocyclic group, a C1-C20 alkynyl group, a C6-C20-aryl-containing hetero group or a silyl group.

[0043]

Also, the metallocene compound of Chemical Formulas 2 to 6 may include a compound substituted through a hydroaddition reaction, and a preferred example thereof includes dimethylsilyl bis(tetrahydroindenyl) zirconium dichloride.

[0044]

The organometallic compound included in the single-site catalyst system may be at least one selected from the group consisting of an organoaluminum compound, an organomagnesium compound, an organozinc compound and an organolithium compound, and is preferably an organoaluminum compound. The organoaluminum compound may be at least one selected from the group consisting of, for example, trimethylaluminum, triethylaluminum, triisobutylaluminum, tripropylaluminum, tributylaluminum, dimethylchloroaluminum, dimethylisobutylaluminum, dimethylethylaluminum, diethylchloroaluminum, triisopropylaluminum, triisobutylaluminum, tricyclopentylaluminum, tripentylaluminum, triisopentylaluminum, ethyldimethylaluminum, methyldiethylaluminum, triphenylaluminum, methylaluminoxane, ethylaluminoxane, isobutylaluminoxane and butylaluminoxane, and is preferably triisobutylaluminum.

[0045]

The ionic compound included in the single-site catalyst system may be at least one selected from the group consisting of organoboron compounds such as dimethylanilinium tetrakis(perfluorophenyl)borate, triphenylcarbenium tetrakis(perfluorophenyl)borate, and the like.

[0046]

The component ratio of the single-site catalyst system may be determined in consideration of catalytic activity, and the molar ratio of metallocene catalyst:ionic compound:organometallic compound is preferably adjusted in the range of 1:1:5 to 1:10:1000 in order to ensure desired catalytic activity.

[0047]

Furthermore, the components of the single-site catalyst system may be added at the same time or in any sequence to an appropriate solvent and may thus function as an active catalyst system. Here, the solvent may include, but is not limited to, a hydrocarbon solvent such as pentane, hexane, heptane, etc., or an aromatic solvent such as benzene, toluene, xylene, etc., and any solvent usable in the preparation may be used.

[0048]

Also, the alphaolefin monomer used in the preparation of the liquid olefin copolymer includes a C2-C20 aliphatic olefin, and may specifically be at least one selected from the group consisting of ethylene, propylene, 1-butene, 1-pentene, 3-methyl-1-butene, 1-hexene, 4-methyl-1-pentene, 3-methyl-1-pentene, 1-heptene, 1-octene, 1-decene, 1-dodecene and 1-tetradecene, and may include isomeric forms, but the present invention is not limited thereto. In the copolymerization, the monomer content is 1 to 95 mol %, preferably 5 to 90 mol %.

[0049]

The liquid olefin copolymer required in the present invention has a coefficient of thermal expansion of 3.0 to 4.0 and a bromine number of 0.1 or less.

[0050]

The liquid olefin copolymer may be included in an amount of 0.1 to 30 wt %, and preferably 0.5 to 25 wt %, based on 100 wt % of the lubricant composition. If the amount of the liquid olefin copolymer is less than 0.1 wt % based on 100 wt % of the lubricant composition, low-temperature stability may deteriorate. On the other hand, if the amount thereof exceeds 30 wt %, sufficient viscosity cannot be realized, and thus application of the resulting composition to gear oil becomes difficult, which is undesirable.

[0051]

The alkylated phosphonium compound, serving as a friction-reducing agent, may be at least one selected from the group consisting of tetraoctylated phosphonium bisethylhexyl phosphate, tributyltetradecylphosphonium bis(2-ethylhexyl)phosphate, tetraethylphosphonium bis(2-ethylhexyl)phosphate and tributylphosphonium bis(2-ethylhexly)phosphate. When the alkylated phosphonium compound is included in the lubricant composition, it may exhibit synergistic effects with an existing wear-resistant agent and friction reduction effects, and additionally, energy-saving effects may be achieved through friction reduction.

[0052]

The alkylated phosphonium compound may be included in an amount of 0.1 to 5.0 wt %, and preferably 0.3 to 4.0 wt %, based on 100 wt % of the lubricant composition. If the amount of the alkylated phosphonium compound is less than 0.1 wt % based on 100 wt % of the lubricant composition, the friction reduction effect is insignificant. On the other hand, if the amount thereof exceeds 5.0 wt %, the additional reduction effect is insignificant despite the excessive addition thereof, which is undesirable.

[0053]

The lubricant composition of the present invention may further include an additive selected from the group consisting of an antioxidant, a metal cleaner, an anticorrosive agent, a foam inhibitor, a pour-point depressant, a viscosity modifier, a wear-resistant agent and combinations thereof.

[0054]

The antioxidant may be included in an amount of 0.01 to 5.0 wt % based on 100 wt % of the lubricant composition, and is preferably used in the form of a mixture of a phenolic antioxidant and an aminic antioxidant, more preferably a mixture of 0.01 to 3.0 wt % of the phenolic antioxidant and 0.01 to 3.0 wt % of the aminic antioxidant.

[0055]

The phenolic antioxidant may be any one selected from the group consisting of 2,6-dibutylphenol, hindered bisphenol, high-molecular-weight hindered phenol, and hindered phenol with thioether.

[0056]

The aminic antioxidant may be any one selected from the group consisting of diphenylamine, alkylated diphenylamine and naphthylamine, and preferably, the alkylated diphenylamine is dioctyldiphenylamine, octylated diphenylamine, or butylated diphenylamine.

[0057]

The metal cleaner may be at least one selected from the group consisting of metallic phenate, metallic sulfonate, and metallic salicylate, and preferably, the metal cleaner is included in an amount of 0.1 to 10.0 wt % based on 100 wt % of the lubricant composition.

[0058]

The anticorrosive agent may be a benzotriazole derivative, and is preferably any one selected from the group consisting of benzotriazole, 2-methylbenzotriazole, 2-phenylbenzotriazole, 2-ethylbenzotriazole and 2-propylbenzotriazole. The anticorrosive agent may be included in an amount of 0 to 4.0 wt % based on 100 wt % of the lubricant composition.

[0059]

The foam inhibitor may be polyoxyalkylene polyol, and preferably, the foam inhibitor is included in an amount of 0 to 4.0 wt % based on 100 wt % of the lubricant composition.

[0060]

The pour-point depressant may be poly(methyl methacrylate), and preferably, the pour-point depressant is included in an amount of 0.01 to 5.0 wt % based on 100 wt % of the lubricant composition.

[0061]

The viscosity modifier may be polyisobutylene or polymethacrylate, and preferably, the viscosity modifier is included in an amount of 0 to 15 wt % based on 100 wt % of the lubricant composition.

[0062]

The wear-resistant agent may be at least one selected from the group consisting of organic borates, organic phosphites, organic sulfur-containing compounds, zinc dialkyl dithiophosphate, zinc diaryl dithiophosphate and phosphosulfurized hydrocarbon, and preferably, the wear-resistant agent is included in an amount of 0.01 to 3.0 wt %.

[0063]

The lubricant composition of the present invention has an SRV friction coefficient of 0.2 to 0.3 and a traction coefficient of 0.15 to 0.3. Also, the lubricant composition of the present invention has a pinion torque loss rate due to friction of less than 1%, as measured through an FZG gear efficiency test as a gear oil rig test.

[0064]

A better understanding of the present invention through the following examples. However, the present invention is not limited to these examples, but may be embodied in other forms. These examples are provided to thoroughly explain the invention and to sufficiently transfer the spirit of the present invention to those skilled in the art.

[0065]

1. Preparation of Additive Composition

[0066]

An additive composition for use in the lubricant composition of the present invention was prepared as shown in Table 2 below.

[0000]

Antioxidant2,6-dibutylphenol11.5
Diphenylamine0.81
Metal cleanerMetallic phenate0.20.6
AnticorrosiveBenzotriazole0.31.0
agent
Foam inhibitorPolyoxyalkylene polyol0.010.02
Pour-pointPolymethylmethacrylate0.20.5
depressant
ViscosityPolyisobutylene1.0
modifier
Wear-resistantZinc diaryl 0.21.1
agentdithiophosphate

[0067]

2. Liquid Olefin Copolymer

[0068]

A liquid olefin copolymer was prepared using an oligomerization method through a catalytic reaction process. Depending on the reaction time and conditions, which follow, liquid olefin copolymers having different molecular weights were prepared, and the properties thereof are shown in Table 3 below.

[0069]

The reaction time and conditions were increased by 4 hr each from 20 hr. Here, the amounts of hydrogen and comonomer C3, which were added thereto, were increased by 10% each, and polymerization was performed under individual conditions, and the resulting polymers were classified depending on the molecular weight thereof.

[0000]

Main properties
AlphaolefinEvaporation Thickening PowerCoE of
copolymerLoss (%)(10 wt % in 150N)Thermal Expansion
Copolymer I1.2863.00 to 3.20
Copolymer II0.5473.20 to 3.40
Copolymer III0.1083.40 to 3.50
Copolymer IV0.001103.50 to 3.60
Copolymer V0.0001123.60 to 3.70
Copolymer VI0.00001143.70 to 3.80

[0070]

3. Preparation of Lubricant Composition For Gear Oil

[0071]

A lubricant composition was prepared by mixing a base oil, the liquid olefin copolymer, an alkylated phosphonium compound, and the additive prepared above, as shown in Tables 4 and 5 below. Here, the base oil was polyalphaolefin (PAO 4 cSt, available from Chevron Philips) having kinematic viscosity of 4 cSt at 100° C., and the alkylated phosphonium compound was tetraoctylated phosphonium bisethylhexyl phosphate.

[0072]

Preparation Examples 1 to 72 and Comparative Examples 1 to 9. Lubricant Composition For Gear Oil Including Additive A

[0000]

Preparation97.14Copolymer I0.12.71
Example 10.05
Preparation96.74Copolymer I0.52.71
Example 20.05
Preparation96.24Copolymer I1.02.71
Example 30.05
Preparation94.24Copolymer I3.02.71
Example 40.05
Preparation92.24Copolymer I5.02.71
Example 50.05
Preparation95.79Copolymer I1.02.71
Example 60.5
Preparation93.79Copolymer I3.02.71
Example 70.5
Preparation91.79Copolymer I 50.52.71
Example 8
Preparation89.29Copolymer I 53.02.71
Example 9
Preparation87.29Copolymer I 55.02.71
Example 10
Preparation86.79Copolymer I 100.52.71
Example 11
Preparation86.29Copolymer I 101.02.71
Example 12
Preparation82.29Copolymer I 105.02.71
Example 13
Preparation76.79Copolymer I 200.52.71
Example 14
Preparation72.29Copolymer I 205.02.71
Example 15
Preparation67.19Copolymer I 300.12.71
Example 16
Preparation62.29Copolymer I 305.02.71
Example 17
Preparation61.79Copolymer I 350.52.71
Example 18
Preparation61.29Copolymer I 351.02.71
Example 19
Preparation59.29Copolymer I 353.02.71
Example 20
Preparation57.29Copolymer I 355.02.71
Example 21
Preparation52.29Copolymer I 3510.02.71
Example 22
Preparation97.14Copolymer II0.12.71
Example 230.05
Preparation96.74Copolymer II0.52.71
Example 240.05
Preparation96.24Copolymer II1.02.71
Example 250.05
Preparation94.24Copolymer II3.02.71
Example 260.05
Preparation92.24Copolymer II5.02.71
Example 270.05
Preparation95.79Copolymer II1.02.71
Example 280.5
Preparation93.79Copolymer II3.02.71
Example 290.5
Preparation91.79Copolymer II 50.52.71
Example 30
Preparation91.29Copolymer II 51.02.71
Example 31
Preparation87.29Copolymer II 55.02.71
Example 32
Preparation87.19Copolymer II0.12.71
Example 3310
Preparation86.29Copolymer II1.02.71
Example 3410
Preparation84.29Copolymer II3.02.71
Example 3510
Preparation82.29Copolymer II5.02.71
Example 3610
Preparation77.19Copolymer II0.12.71
Example 3720
Preparation74.29Copolymer II3.02.71
Example 3820
Preparation72.29Copolymer II5.02.71
Example 3920
Preparation67.19Copolymer II0.12.71
Example 4030
Preparation97.14Copolymer III0.12.71
Example 410.05
Preparation96.74Copolymer III0.52.71
Example 420.05
Preparation96.24Copolymer III1.02.71
Example 430.05
Preparation94.24Copolymer III3.02.71
Example 440.05
Preparation91.79Copolymer III0.52.71
Example 455
Preparation87.29Copolymer III5.02.71
Example 465
Preparation86.79Copolymer III0.52.71
Example 4710
Preparation82.29Copolymer III5.02.71
Example 4810
Preparation76.79Copolymer III0.52.71
Example 4920
Preparation76.29Copolymer III1.02.71
Example 5020
Preparation72.29Copolymer III5.02.71
Example 5120
Preparation92.19Copolymer IV 50.12.71
Example 52
Preparation89.29Copolymer IV 53.02.71
Example 53
Preparation87.29Copolymer IV 55.02.71
Example 54
Preparation82.29Copolymer IV 510.02.71
Example 55
Preparation86.79Copolymer IV0.52.71
Example 5610
Preparation74.29Copolymer IV3.02.71
Example 5720
Preparation76.79Copolymer IV0.52.71
Example 5820
Preparation91.79Copolymer V 50.52.71
Example 59
Preparation86.79Copolymer V 100.52.71
Example 60
Preparation82.29Copolymer V 105.02.71
Example 61
Preparation77.19Copolymer V 200.12.71
Example 62
Preparation76.79Copolymer V 200.52.71
Example 63
Preparation72.29Copolymer V 205.02.71
Example 64
Preparation67.19Copolymer V 300.12.71
Example 65
Preparation66.79Copolymer V 300.52.71
Example 66
Preparation97.14Copolymer VI0.12.71
Example 670.05
Preparation96.74Copolymer VI0.52.71
Example 680.05
Preparation96.24Copolymer VI1.02.71
Example 690.05
Preparation91.79Copolymer VI 50.52.71
Example 70
Preparation86.79Copolymer VI0.52.71
Example 7110
Preparation76.79Copolymer VI0.52.71
Example 7220
Comparative97.24Copolymer I2.71
Example 10.05
Comparative97.24Copolymer II2.71
Example 20.05
Comparative87.29Copolymer II2.71
Example 310
Comparative77.29Copolymer II2.71
Example 420
Comparative67.29Copolymer II2.71
Example 530
Comparative92.29Copolymer IV 52.71
Example 6
Comparative67.29Copolymer V 302.71
Example 7
Comparative62.29Copolymer V 352.71
Example 8
Comparative97.24Copolymer VI2.71
Example 90.05

[0073]

Preparation Examples 73 to 148 and Comparative Examples to 16. Lubricant Composition For Gear Oil Including Additive B

[0000]

Preparation92.28Copolymer I0.56.72
Example 730.5
Preparation91.78Copolymer I1.06.72
Example 740.5
Preparation87.78Copolymer I 50.56.72
Example 75
Preparation87.28Copolymer I 51.06.72
Example 76
Preparation82.28Copolymer I1.06.72
Example 7710
Preparation80.28Copolymer I3.06.72
Example 7810
Preparation72.78Copolymer I0.56.72
Example 7920
Preparation72.28Copolymer I1.06.72
Example 8020
Preparation91.78Copolymer II1.06.72
Example 810.5
Preparation89.78Copolymer II3.06.72
Example 820.5
Preparation87.78Copolymer II0.56.72
Example 835
Preparation87.28Copolymer II1.06.72
Example 845
Preparation82.28Copolymer II1.06.72
Example 8510
Preparation80.28Copolymer II3.06.72
Example 8610
Preparation70.28Copolymer II3.06.72
Example 8720
Preparation62.78Copolymer II0.56.72
Example 8830
Preparation62.28Copolymer II1.06.72
Example 8930
Preparation60.28Copolymer II3.06.72
Example 9030
Preparation58.28Copolymer II5.06.72
Example 9130
Preparation93.13Copolymer III0.16.72
Example 910.05
Preparation92.73Copolymer III0.56.72
Example 930.05
Preparation92.23Copolymer III1.06.72
Example 940.05
Preparation90.23Copolymer III3.06.72
Example 950.05
Preparation87.78Copolymer III0.56.72
Example 965
Preparation83.28Copolymer III5.06.72
Example 975
Preparation82.78Copolymer III0.56.72
Example 9810
Preparation78.28Copolymer III5.06.72
Example 9910
Preparation72.78Copolymer III0.56.72
Example 10020
Preparation72.28Copolymer III1.06.72
Example 10120
Preparation68.28Copolymer III5.06.72
Example 10220
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Example 10330
Preparation58.18Copolymer III0.16.72
Example 10435
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Example 10535
Preparation57.28Copolymer III1.06.72
Example 10635
Preparation55.28Copolymer III3.06.72
Example 10735
Preparation93.13Copolymer IV0.16.72
Example 1080.05
Preparation92.73Copolymer IV0.56.72
Example 1090.05
Preparation92.23Copolymer IV1.06.72
Example 1100.05
Preparation90.23Copolymer IV3.06.72
Example 1110.05
Preparation88.23Copolymer IV5.06.72
Example 1120.05
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Example 1135
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Example 1145
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Example 1155
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Example 1165
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Example 11710
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Example 11810
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Example 11910
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Example 12020
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Example 12120
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Example 12220
Preparation93.13Copolymer V0.16.72
Example 1230.05
Preparation92.73Copolymer V0.56.72
Example 1240.05
Preparation92.23Copolymer V1.06.72
Example 1250.05
Preparation90.23Copolymer V3.06.72
Example 1260.05
Preparation88.23Copolymer V5.06.72
Example 1270.05
Preparation88.18Copolymer V 50.16.72
Example 128
Preparation87.78Copolymer V 50.56.72
Example 129
Preparation83.28Copolymer V 55.06.72
Example 130
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Example 13110
Preparation78.28Copolymer V5.06.72
Example 13210
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Example 13320
Preparation72.28Copolymer V1.06.72
Example 13420
Preparation63.18Copolymer V0.16.72
Example 13530
Preparation90.23Copolymer VI3.06.72
Example 1360.05
Preparation88.23Copolymer VI5.06.72
Example 1370.05
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Example 1385
Preparation85.28Copolymer VI3.06.72
Example 1395
Preparation83.18Copolymer VI0.16.72
Example 14010
Preparation82.28Copolymer VI1.06.72
Example 14110
Preparation78.28Copolymer VI5.06.72
Example 14210
Preparation70.28Copolymer VI3.06.72
Example 14320
Preparation58.18Copolymer VI0.16.72
Example 14435
Preparation57.78Copolymer VI0.56.72
Example 14535
Preparation57.28Copolymer VI1.06.72
Example 14635
Preparation55.28Copolymer VI3.06.72
Example 14735
Preparation53.28Copolymer VI5.06.72
Example 14835
Comparative93.23Copolymer IV6.72
Example 100.05
Comparative88.28Copolymer IV6.72
Example 115
Comparative83.28Copolymer IV6.72
Example 1210
Comparative88.28Copolymer V 56.72
Example 13
Comparative73.28Copolymer V6.72
Example 1420
Comparative63.28Copolymer V
Example 15306.72
Comparative88.28Copolymer VI
Example 1656.72

[0074]

4. Evaluation of Properties

[0075]

The properties of the lubricant compositions prepared in Preparation Examples and Comparative Examples were measured as follows. The results are shown in Tables 6 and 7 below.

[0076]

Friction Coefficient

[0077]

In the ball-on-disc mode, friction performance was evaluated by sequentially elevating the temperature in increments of 100□ from 40 to 120□ at 50 Hz and comparing the average friction coefficients at individual temperatures. Here, the friction coefficient value decreases with an increase in effectiveness.

[0078]

Traction Coefficient

[0079]

The traction coefficient was measured using an MTM instrument made by PCS Instruments. Here, the measurement conditions were fixed at 50N and SRR 50%, and friction and traction were observed depending on changes in temperature. The temperature was varied from 40 to 120□, and the average values were compared.

[0080]

Wear Resistance

[0081]

Four steel balls were subjected to friction with the lubricant composition for 60 min under conditions of 20 kg load, 1200 rpm, and 54□, the sizes of wear scars were compared, and evaluation was carried out in accordance with ASTM D4172. Here, the wear scar (average wear scar diameter, μm) value decreases with an increase in effectiveness.

[0082]

Oxidation Stability

[0083]

Oxidation stability was measured using an RBOT (Rotational Bomb Oxidation Test) meter in accordance with ASTM D2271.

[0084]

Friction Loss

[0085]

As a gear oil rig test, an FZG gear efficiency test was performed. In the FZG efficiency test, the pinion torque was measured through rotation with a motor drive specified depending on the type of oil under conditions in which the temperature of oil was fixed to 100° C. and no load was applied, and thus the pinion torque loss rates of existing oil and the oil using the alphaolefin copolymer and the alkylated phosphonium compound were calculated, and relative values thereof were compared.

[0000]

Preparation0.7010.5984966101.20
Example 1
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[0000]

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Example 15
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Example 16

[0086]

As is apparent from Tables 6 and 7, the lubricant compositions including the liquid olefin copolymer and the alkylated phosphonium compound within the amount ranges of the present invention were significantly reduced in wear scar and friction coefficient compared to the lubricant compositions of Comparative Examples, and also exhibited superior oxidation stability.

[0087]

Moreover, an efficiency improvement of at least 5 to 12% in the FZG gear efficiency test resulted, indicating that, even in practical use, the lubricant composition of the present invention was capable of reducing gear loss, thereby significantly improving fuel economy or energy-saving effects.

[0088]

Therefore, it is concluded that the lubricant composition of the present invention is improved from the aspects of friction characteristics and stability and thus is suitable for use in gear oil.

[0089]

Although the embodiments of the present invention have been disclosed for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims.



The present invention relates to a lubricant composition, and more particularly to a lubricant composition, which includes an ethylene-alphaolefin oligomer and an alkylated phosphonium compound, thus realizing energy reduction and an increased endurance life, and which is thus suitable for use in gear oil. The lubricant composition of the present invention includes a base oil, a liquid olefin copolymer, and an alkylated phosphonium compound.



1. A lubricant composition, comprising:

a base oil, a liquid olefin copolymer, and an alkylated phosphonium compound.

2. The lubricant composition of claim 1, wherein the liquid olefin copolymer is prepared by copolymerizing ethylene and alphaolefin using a single-site catalyst system.

3. The lubricant composition of claim 2, wherein the single-site catalyst system includes a metallocene catalyst, an organometallic compound and an ionic compound.

4. The lubricant composition of claim 1, wherein the liquid olefin copolymer has a coefficient of thermal expansion of 3.0 to 4.0.

5. The lubricant composition of claim 1, wherein the liquid olefin copolymer has a bromine number of 0.1 or less.

6. The lubricant composition of claim 1, wherein the alkylated phosphonium compound is included in an amount of 0.1 to 5.0 wt % in the lubricant composition.

7. The lubricant composition of claim 1, wherein the liquid olefin copolymer is included in an amount of 0.1 to 30 wt % in the lubricant composition.

8. The lubricant composition of claim 1, wherein the base oil is at least one selected from the group consisting of mineral oil, polyalphaolefin (PAO), and ester.

9. The lubricant composition of claim 1, further comprising an additive selected from the group consisting of an antioxidant, a metal cleaner, an anticorrosive agent, a foam inhibitor, a pour-point depressant, a viscosity modifier, a wear-resistant agent, and combinations thereof.

10. The lubricant composition of claim 1, wherein the lubricant composition has an SRV friction coefficient of 0.2 to 0.3.

11. The lubricant composition of claim 1, wherein the lubricant composition has a traction coefficient of 0.15 to 0.3.

12. The lubricant composition of claim 1, wherein the lubricant composition has a pinion torque loss rate due to friction of less than 1% in an FZG gear efficiency test.

13. The lubricant composition of claim 1, wherein the lubricant composition is used as gear oil.