US20040058830A1

US20040058830A1 - Additive for lubricating oil and lubricating oil composition

Info

Publication number: US20040058830A1
Application number: US10/250,311
Authority: US
Inventors: Kojiro Kan; Toshiyuki Ito; Kunihiko Takeuchi; Hideki Hirano
Original assignee: Mitsui Chemicals Inc
Current assignee: Mitsui Chemicals Inc
Priority date: 2001-11-01
Filing date: 2002-10-31
Publication date: 2004-03-25
Also published as: CN1494582A; JPWO2003038017A1; KR20040062422A; KR100518425B1; EP1441023A4; EP1441023A1; CN100415858C; WO2003038017A1

Abstract

The present invention is intended to provide a lubricating oil additive having high viscosity index improvability and shear stability and a lubricating oil composition containing the additive and having excellent viscosity index and excellent shear stability. The lubricating oil additive comprises an ethylene/α-olefin random copolymer having the following properties:

(i) said copolymer is a copolymer of ethylene and at least one α-olefin selected from α-olefins of 3 to 20 carbon atoms and contains at least constituent units derived from ethylene in amounts of 10 to 75% by mol and constituent units derived from at least one α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 20 to 80% by mol,

(ii) the kinematic viscosity at 100° C. is in the range of 500 to 1,000,000 mm²/s,

(iii) the intrinsic viscosity [η] is in the range of 0.15 to 11.0 dl/g,

(iv) the molecular weight distribution (Mw/Mn), as measured by GPC, is not more than 4, and

(v) the number-average molecular weight is in the range of 5,000 to 30,000.

Description

TECHNICAL FIELD

The present invention relates to an ethylene/α-olefin random copolymer useful as an additive having high viscosity index and hardly suffering viscosity decrease attributable to permanent or temporary shear, a lubricating oil composition containing the copolymer.

BACKGROUND ART

An ethylene/propylene copolymer is well known as a lubricating oil additive comprising an ethylene random copolymer. Since this ethylene/propylene copolymer has no unsaturated double bond and few tertiary carbon atoms, it exhibits excellent shear stability and oxidation stability. Therefore, when this copolymer is added-to a lubricating oil, such as gear oil, engine oil or grease, the life of the oil is prolonged, and hence the copolymer is widely employed.

Further, it is known that when the copolymer is added as a thickening agent to a lubricating oil containing a synthetic hydrocarbon or an ester as a base oil, the low-temperature viscosity of the oil is decreased,(Japanese Patent Laid-Open Publication No. 104695/1989).

However, the lubricating oil containing a mineral oil or a hydrocarbon synthetic oil as a base oil and an ethylene/propylene copolymer as a thickening agent has a viscosity index lower than that of a lubricating oil containing PMA (polymethyl methacrylate). On this account, the temperature dependence of the viscosity of the lubricating oil is great, and if the high-temperature viscosity of the lubricating oil is designed so as to be kept constant at a certain value, the low-temperature viscosity is increased, and therefore the use of the lubricating oil in winter or in the cold district is sometimes restricted. Accordingly, a thickening agent having high viscosity index improvability is desired.

The viscosity index improvability of an ethylene random copolymer generally depends upon the molecular weight, and if the molecular weight is increased, the viscosity index improvability is also increased but the shear stability is decreased. If the ethylene content is increased, the viscosity index improvability and the shear stability are both enhanced, but the high-ethylene content portion is crystallized to make the compounded oil turbid, and hence the compounded oil cannot be used as a lubricating oil.

On the other hand, it is generally known that PMA has high viscosity index but has low shear stability.

Under such circumstances as mentioned above, the present inventors have made various studies of the types and the amounts of comonomers in ethylene random copolymers. As a result, they have found that an ethylene/α-olefin random copolymer, which has specific ranges of an α-olefin content, a kinematic viscosity at 100° C., an intrinsic viscosity [η], and a molecular weight distribution and a number-average molecular weight as measured by gel permeation chromatography, has both of high viscosity index improvability and excellent shear stability and is favorable as an additive to a lubricating oil. That is to say, the present inventors have found that an ethylene/α-olefin copolymer having many branched chains of 6 or more carbon atoms has both of high viscosity index improvability and excellent shear stability.

In WO 01/85880A1, there is disclosed a viscosity modifier for lubricating oil, which is a copolymer of ethylene, an α-olefin of 3 or more carbon atoms and a higher α-olefin of 4 to 20 carbon atoms whose number of carbon atoms is larger by 1 or more than that of the α-olefin of 3, or more carbon atoms, contains 40 to 80% by weight of ethylene, 15 to 59% by weight of the α-olefin of 3 or more carbon atoms and 0.1 to 25% by weight of the higher α-olefin of 4 to 20 carbon atoms (total: 100% by weight), and has a weight-average molecular weight of 80,000 to 400,000. This-copolymer, however, has an α-olefin content lower than that of the ethylene/α-olefin copolymer of the present invention.

It is an object of the present invention to provide a lubricating oil additive having high viscosity index improvability and shear stability and a lubricating oil, composition excellent in viscosity index and shear stability.

DISCLOSURE OF THE INVENTION

According to the present invention, the following lubricating oil thickening agent and lubricating oil composition capable of attaining-the above object can be provided.

(1) A lubricating oil additive comprising an ethylene/α-olefin random copolymer having the following properties:

(ii) the kinematic viscosity at 100° C. is in the range of 500 to 1,000,000 mm ²/s,

(iii) the intrinsic viscosity [η], as measured in decalin at 135° C., is in the range of 0.15 to 1.0 dl/g,

(iv) the molecular weight distribution (Mw/Mn, Mw: weight-average molecular weight, Mn: number-average molecular weight), as measured by gel permeation chromatography, is not more than 4, and

(v) the number-average molecular weight is in the range of 5,000 to 30,000.

(2) The lubricating oil additive as stated in the above (1), wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 30 to 75% by mol and constituent units derived from at least one α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 25 to 70% by mol.

(3) The lubricating oil additive as-stated in the above (1), wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 30 to 75% by mol and constituent units derived from at least one α-olefin selected from α-olefins of 10 to 16 carbon atoms in amounts of 25 to 70% by mol.

(4) The lubricating oil additive as stated in the above (1), wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 35 to 70% by mol and constituent units derived from 1-decene in amounts of 30 to 65% by mol.

(5) The lubricating oil additive as stated in the above (1), wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 10 to 75% by mol, constituent units derived from at least one lower α-olefin selected from α-olefins of 3 to 6 carbon atoms in amounts of 5 to 50% by mol, and constituent units derived from at least one higher α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 20 to 85% by mol.

(6) The lubricating oil additive as stated in the above (1), wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 10 to 70% by mol, constituent units derived from at least one lower α-olefin selected from α-olefins of 3 to 6 carbon atoms in amounts of 10 to 40% by mol, and constituent units derived from at least one higher α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 20 to 80% by mol.

(7) The lubricating oil additive as stated in the above.(1), wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 10 to. 70% by mol, constituent units derived from at least one lower α-olefin selected from α-olefins of 3 to 4 carbon atoms in amounts of 10 to 40% by mol, and constituent units derived from at least one higher α-olefin selected from α-olefins of 10 to 14 carbon atoms in amounts of 20 to 80% by mol.

(8) The lubricating oil additive as stated in the above (1), wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 10 to 70% by mol, constituent units derived from propylene in amounts of 10 to 40% by mol, and constituent units derived from 1-decene in amounts of 20 to 80% by mol.

(9) A lubricating oil additive containing constituent units derived from ethylene in amounts of 30 to 75% by mol and constituent units derived from at least one α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 25 to 70% by mol, and having the following properties:

the shear stability (A (%)) and the viscosity index (B) satisfy the following formula:

B≧0.4×A+155

and

A is a number-satisfying the condition of A≦30.

(10) The lubricating oil additive as stated in the above (9), wherein the shear stability (A (%)) and the low-temperature viscosity (C (mPa·s)) as measured at −26° C. satisfy the following formula:

C≦−50×A+15,000.

(11) A lubricating oil composition comprising:

(A) at least one base oil selected from a synthetic hydrocarbon, a mineral oil and an ester, which has a kinematic viscosity at 100° C. of 1 to 20 mm ²/s, in an amount of 50 to 99.8 parts by weight,

(B) the lubricating oil additive as stated in any one of the above (1) to (10), in an amount of 0.2 to 50 parts by weight,

with the proviso that the total of the component (A) and the component (B) is 100 parts by weight,

and optionally,

(C) at least one additive selected from the group consisting of a dispersant, a viscosity index improver, an antioxidant, a corrosion inhibitor, an anti-wear agent, a pour point depressant, a rust preventive, an anti-foaming agent and an extreme pressure agent.

BEST MODE FOR CARRYING OUT THE INVENTION

The lubricating oil additive and the lubricating oil composition according to the invention are described in detail hereinafter.

The lubricating oil additive according to the invention comprises a liquid ethylene/α-olefin random copolymer.

The ethylene/α-olefin random copolymer is a copolymer of ethylene and at least one α-olefin selected from α-olefins of 3 to 20, carbon atoms and contains at least constituent units derived from ethylene and Constituent units derived from at least one α-olefin selected from α-olefins of 8 to 20 carbon atoms.

The ethylene/α-olefin random copolymer that is a lubricating oil thickening agent of the invention satisfies the following requirements (i) to (v).

(i) The ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 10 to 75% by mol and constituent units derived from at least one α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 20 to 80% by mol.

In a preferred embodiment of the invention, the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 30 to 75%by mol, preferably 35 to 70% by mol, more preferably 50 to 70% by mol, and constituent units derived from an α-olefin of 8 to 20 carbon atoms in amounts of 25 to 70% by mol, preferably 30 to 65% by mol, more preferably 30 to 50% by mol (copolymer (i-a))

In another preferred embodiment of the invention, the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 10 to 75% by mol, preferably 10 to 70% by mol, constituent units derived from at least one lower α-olefin selected from α-olefins of 3 to 6 carbon atoms in amounts of 10 to 50% by mol, preferably 10 to 40% by mol, and constituent units derived from at least one higher α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 20 to 85% by mol, preferably 20 to 80% by mol (copolymer (i-b)).

Examples of the α-olefins of 3 to 6 carbon atoms (lower α-olefins) include straight-chain α-olefins, such as propylene, 1-butene, 1-pentene and 1-hexene, and branched α-olefins, such as isobutylene, 3-methyl-1-butene and 4-methyl-1-pentene.

Examples of the α-olefins of 8 to 20 carbon atoms (higher α-olefins) include straight-chain α-olefins, such as 1-octene, 1-decene, 1-undecene, 1-dodecene, 1-tridecene, 1-tetradecene, 1-pentadecene, 1-hexadecene, 1-heptadecene, 1-octadecene, 1-nonadecene and 1-eicosene, and branched α-olefins, such as 8-methyl-1-nonene, 7-methyl-1-decene, 6-methyl-1-undecene and 6,8-dimethyl-1-decene.

In the copolymer (i-a), the α-olefin of 8 to 20 carbon atoms is preferably an α-olefin of 8 to 16 carbon atoms, more preferably an α-olefin of 10 to 16 carbon atoms, still more preferably an α-olefin of 10 to 12 carbon atoms, particularly preferably 1-decene.

In the copolymer (i-a), two of more kinds of α-olefins of 8 to 20 carbon atoms are employable, and for example, a combination of 1-decene and 1-dodecene and a combination of 1-decene and 1-tetradecene are preferable.

In the copolymer (i-a), an α-olefin of 3 to 7 carbon atoms may be copolymerized in a small amount (e.g., not more than 3% by mol).

In the copolymer (i-b), the lower α-olefin is preferably an α-olefin of 3 or 4 carbon atoms, particularly preferably propylene. In the copolymer (i-b), the higher α-olefin is preferably an α-olefin of 8 to 16 carbon atoms, more preferably an α-olefin of 10 to 14 carbon atoms, still more preferably an α-olefin of 10 to 12 carbon atoms, particularly preferably 1-decene.

In the copolymer (i-b)., two or more kinds of lower α-olefins are employable, and two or more kinds of higher α-olefins are employable.

When the ethylene content in the ethylene/α-olefin random copolymer is in the above range, the copolymer has excellent shear stability and high viscosity index improvability. Moreover, the copolymer does not become turbid, and the pour point thereof can be maintained low.

(ii) The kinematic viscosity at 100° C. (JIS K 2283) is in the range of 0.500 to 1,000,000 mm ²/s, preferably 500 to 500,000 mm²/s, more preferably 1,000 to 100,000 mm²/s.

When the kinematic-viscosity of the ethylene/α-olefin random copolymer at 100° C. is in the above range, the copolymer exhibits an excellent balance between the shear stability and the viscosity index, so that it is practically desirable.

(iii) The intrinsic viscosity [i], as measured in decalin at 135° C., is in the range of 0.15 to 1.0 dl/g, preferably 0.15 to 0.8 dl/g.

When the intrinsic viscosity [η] of the ethylene/α-olefin random copolymer is in the above range, the copolymer exhibits an excellent balance between the shear stability and the viscosity index, so that it is practically desirable.

(iv) The number-average molecular weight (Mn), as measured by GPC (molecular weight standard substance: polystyrene), is in the range of 5,000 to 30,000, preferably 5,000 to 27,000, more preferably 8,000 to 27,000, still more preferably 10,000 to 25,000.

When the number-average molecular weight of the ethylene/α-olefin random copolymer is in the above range, the copolymer exhibits an excellent balance between the shear stability and the viscosity index, so that it is practically desirable.

(v) The molecular weight distribution (Mw/Mn, Mw: weight-average molecular weight, Mn: number-average molecular weight), as measured by GPC, is not more than 4, preferably not more than 3.5

When Mw/Mn of the ethylene/α-olefin random copolymer is in the above range, the copolymer has excellent shear stability.

When the ethylene/α-olefin random copolymer is the copolymer (i-a), this copolymer can become a thickening agent having high viscosity index improvability and shear stability. By blending this thickening agent, a lubricating oil composition excellent in viscosity index and shear stability and particularly free from turbidity can be obtained.

When the ethylene/α-olefin random copolymer is the copolymer (i-b), this copolymer can become a thickening agent having high viscosity index improvability and shear stability. By blending this thickening agent, a lubricating oil composition excellent in viscosity index and shear stability and particularly having a low pour point can be obtained.

The ethylene/α-olefin random copolymer of the invention that is a lubricating oil thickening agent of the invention preferably satisfies the above requirement (i) and the following requirement (vi), or preferably satisfies the above requirement (i) and the following requirements (vi) and (vii), or preferably satisfies the above requirements (i) to (v) and the following requirements (vi) and (vii). Such an ethylene/α-olefin random copolymer is preferably the copolymer (i-a).

(vi) The shear stability (A (%)) and the viscosity index (B) satisfy the following formula:

B≧0.4×A+155, and

A is a number satisfying the condition of A≦30;

preferably, they satisfy the following formula:

B≧0.4×A+158, and

A is a number satisfying the condition of A≦25;

more preferably, they satisfy the following formula:

0.4×A+180≧B≧0.4×A+158, and

A is a number-satisfying the condition of A≦22.

(vii) The shear stability (A (%)) and the low-temperature viscosity (C (mPa·s)) as measured at −26° C. satisfy the following formula:

C≦−50×A+15,000, and

A is a number satisfying the condition of A≦30;

preferably, they satisfy the following formula:

C≦−50×A+14,000, and

A is a number satisfying the condition of A≦25;

more preferably, they satisfy the following formula:

−50×A+8,000≦C≦−50×A+14,000, and

A is a number satisfying the condition of A≦20.

The ethylene/α-olefin random copolymer satisfying the requirement (vi) and the ethylene/α-olefin random copolymer satisfying the requirements (vi) and (vii) can each become a thickening agent excellent in shear stability and low-temperature viscosity properties.

Methods to measure the shear stability, the viscosity index and the low-temperature viscosity are described later.

Process for Preparing Ethylene/α-Olefin Random Copolymer

The ethylene/α-olefin random copolymer that is a lubricating oil additive of the invention is desired to have a structure wherein the α-olefin units are incorporated into the polymer chain as uniformly as possible. Therefore, it is preferable to prepare the copolymer by the use of a single site catalyst system, and for example, it is preferable to prepare the copolymer by the use of a metallocene catalyst consisting of a metallocene compound and an organoaluminum oxy-compound and/or an ionizing ionic compound. Examples of the metallocene catalysts employable for the preparation of the ethylene/α-olefin random copolymer are given below. As a matter of course, catalysts other than the following ones are employable without any problem as long as they can copolymerize α-olefins of 10 to 20 carbon atoms with high randomness.

Metallocene Compound

The metallocene compound for constituting the metallocene catalyst is a metallocene compound of a transition metal selected from Group 4 of the periodic table and is, for example, a compound-represented by the following formula (1):

ML_x (1)

wherein M is a transition metal selected from the Group 4 of the periodic table, x is a valence of the transition metal M, and L is a ligand.

Examples of the transition metals indicated by M include zirconium, titanium and hafnium. L is a ligand coordinated to the transition metal. At least one ligand L is a ligand having cyclopentadienyl skeleton, and the ligand having cyclopentadienyl skeleton may have a substituent.

Examples of the ligands L having cyclopentadienyl skeleton include cyclopentadenyl group; alkyl- or cycloalkyl-substituted cyclopentadienyl groups, such as methylcyclopentadienyl, ethylcyclopentadienyl, n- or i-propylcyclopentadienyl, n-, i-, sec- or-t-butylcyclopentadienyl, dimethylcyclopentadienyl, methylpropylcyclopentadienyl, methylbutylcyclopentadienyl and methylbenzylcyclopentadienyl; indenyl group; 4,5,6,7-tetrahydtoindenyl group; and fluorenyl group. The hydrogen in the group having cyclopentadienyl skeleton may be replaced with a halogen atom or a trialkylsilyl group.

When the metallocene compound has two or more groups having cyclopentadienyl skeleton as ligands L, two of the groups having cyclopentadienyl skeleton may be bonded to each other through, for example, an alkylene group, such as ethylene or propylene, a substituted alkylene group, such as isopropylidene or diphenylmethylene, a silylene group, or a substituted silylene group, such as methylsilylene, diphenylsilylene or methylphenylsilylene.

Examples of the ligands L (ligands L having no cyclopentadienyl skeleton) other than the ligands having cyclopentadienyl skeleton include a hydrocarbon group of 1 to 12 carbon atoms, an alkoxy group, an aryloxy group, a sulfonic acid-containing group (—SO ₃R¹) (R¹is an alkyl group, an alkyl group substituted with a halogen atom, an aryl group, or an aryl group substituted with a halogen atom or an alkyl group), a halogen atom and a hydrogen atom.

Example 1 of the Metallocene Compound

The metallocene compound represented by the formula (1) wherein the valence of the transition metal is 4 is more specifically represented by the following formula (2):

R² _kR³ _lR⁴ _mR⁵ _nM (2)

wherein M is a transition metal selected from Group 4 of-2 the periodic table, R is a group (ligand) having cyclopentadienyl skeleton, R ³, R⁴and R⁵are each independently a group (ligand) having or not having cyclopentadienyl skeleton, k is an integer of 1 or more, and k+l+m+n=4.

Examples of the metallocene compounds having zirconium as M and containing at least two ligands having cyclopentadienyl skeleton include bis(cyclopentadienyl)zirconium monochloride monohydride, bis(cyclopentadienyl)zirconium dichloride, bis(1-methyl-0.3-butylcyclopentadienyl)zirconium-bis(trifluoromethanesulfonato), bis(1,3-dimethylcyclopentadienyl)zirconium dichloride and bis(n-butylcyclopentadienyl)zirconium dichloride.

Compounds wherein the 1,3-position substituted cyclopentadienyl group in the above compounds is replaced with a 1,2-position substituted cyclopentadienyl group are also employable.

As another example of the metallocene compound, a bridge type metallocene compound of the formula (2) wherein at least two of R ², R³, R⁴and R⁵, for example, R²and R³, are each a group (ligand) having cyclopentadienyl skeleton, and these at least two groups are bonded to each other through an alkylene group, a substituted alkylene group, a silylene group, a substituted silylene group or the like is also employable. In this case, R⁴and R⁵are each independently identical with the aforesaid ligand L other than the ligand having cyclopentadienyl skeleton.

Examples of the bridge type metallocene compounds include ethylenebis(indenyl)dimethylzirconium, ethylenebis(indenyl)zirconium dichloride, isopropylidene(cyclopentadienyl-fluoroenyl)zirconium dichloride, diphenylsilylenebis(indenyl)zirconium dichloride and methylphenylsilylenebis(indenyl)zirconium dichloride.

Example 2 of the Metallocene Compound

Another example of the metallocene compound is a metallocene compound represented by the following formula (3), which is described in Japanese Patent Laid-Open Publication No. 268307/1992.

In the above formula, M is a transition metal of Group 4 of the periodic table, such as titanium, zirconium or hafnium.

R ¹¹and R¹²may be the same or different and are each a hydrogen atom, an alkyl group of 1 to 10 carbon atoms, an alkoxy group of 1 to 10 carbon atoms, an aryl group of 6 to 10 carbon atoms, an aryloxy group of 6 to 10 carbon atoms, an alkenyl group of 2 to 10 carbon atoms, an arylalkyl group of 7 to 40 carbon atoms, an alkylaryl group of 7 to 40 carbon atoms, an aryla-lkenyl group of 8 to 40 carbon atoms, or a halogen atom, preferably a chlorine atom.

R ¹³and R¹⁴may be the same or different and are each a hydrogen atom, a halogen atom, an alkyl group of 1 to −10 carbon atoms which may be halogenated, an aryl group of 6 to 10 carbon atoms, —N(R²⁰)2 group, —SR²⁰group, —OSi(R²⁰)₃group, —Si(R 20)₃group or —P(R²⁰)₂group. R²⁰is a halogen atom, preferably a chorine atom, an alkyl group of 1 to 10 carbon atom, preferably 1 to 3 carbon atoms, or an aryl group of 6 to 10 carbon atoms, preferably 6 to 8 carbon atoms. R¹³and R¹⁴are each particularly preferably a hydrogen atom.

R ¹⁵and R¹⁶are identical with R¹³and R¹⁴except that a hydrogen atom is not included, and they may be the same as or different from each other, preferably the same as each other. R¹⁵and R¹⁶are each preferably an alkyl group of 1 to 4 carbon atoms which may be halogenated, specifically methyl, ethyl, propyl, isopropyl, butyl, isobutyl, trifluoromethyl or the like, particularly preferably methyl.

In the formula (3), R ¹⁷is selected from the group consisting of:

═BR ²¹, AlR²¹, —Ge—, —Sn—, —O—, —S—, ═SO, ═SO₂, ═NR, ═CO, ═PR²¹and ═P(O)R²¹. M¹is silicon, germanium or tin, preferably silicon or germanium.

In the above formulas, R ²¹, R²²and R²³may be the same or different and are each a hydrogen atom, a halogen atom, an alkyl group of 1 to 10 carbon atoms, a fluoroalkyl group of 1 to 10 carbon atoms, an aryl group of 6 to 10 carbon atoms, a fluoroaryl group of 6 to 10 carbon atoms, an alkoxy group of 1 to 10 carbon atoms, an alkenyl group of 2 to 10 carbon atoms, an arylalkyl group of 7 to 40 carbon atoms, an arylalkenyl group of 8 to 40 carbon atoms, or an alkylaryl group of 7 to 40 carbon atoms “R²¹and R²²”or “R²¹and R²³” may form a ring together with atoms to which they are bonded.

R ¹⁷is preferably ═CR²¹R²², ═SiR²¹R²², ═GeR²R²²—O—, —S—, ═SO, ═PR²¹or ═P(O)R²¹.

R ¹⁸and R¹⁹may be the same or different and are each the same group as indicated by R²¹.

m and n may be the same or different and are each 0, 1 or 2, preferably 0 or 1. m+n is 0, 1 or 2, preferably 0 or 1.

Examples of the metallocene compounds represented by the formula (3) include rac-ethylene(2-methyl-1-indenyl) ²_zirconium-dichloride, rac-dimethylsilylene(2-methyl-1-indenyl)²-zirconium-dichloride. These metallocene compounds can be prepared by, for example, the process described in Japanese Patent Laid-Open Publication No. 268307/1992.

Example 3 of the Metallocene Compound

As the metallocene compound, further, a metallocene compound represented by the following formula (4) is-also employable.

In the above formula, M is a transition metal atom of Group 4 of the periodic table, specifically titanium, zirconium or hafnium.

R ²⁴and R²⁵may be the same or different and are each a hydrogen atom, a halogen atom, a hydrocarbon group-of 1 to 20 carbon atoms, a halogenated hydrocarbon group of 1 to 20 carbon atoms, a silicon-containing-group, an oxygen-containing group, a sulfur-containing group, a nitrogen-containing group or a phosphorus-containing group.

R ²⁴is preferably a hydrocarbon group, particularly preferably an alkyl group of 1 to 3 carbon atoms, such as methyl, ethyl or propyl.

R ²⁵is preferably a hydrogen atom or a hydrocarbon group, particularly preferably a hydrogen atom or an alkyl group of 1 to 3 carbon atoms, such as methyl, ethyl or propyl.

R ²⁶, R²⁷, R²⁸and R²⁹may be the same or different and are each a hydrogen atom, a halogen atom, a hydrocarbon group of 1 to 20 carbon atoms or a halogenated hydrocarbon group of 1 to 20 carbon atoms. Of these, hydrogen, a hydrocarbon group or a halogenated hydrocarbon group is preferable. At least one combination of “R²⁶and R²⁷”, “R²⁷and R²⁸” and “R²⁸and R²⁹” may form a monocyclic aromatic ring together with carbon atoms to which they are bonded. When two or more kinds of hydrocarbon groups or halogenated hydrocarbon groups are present in the groups other than the groups for forming the aromatic ring, they may be bonded to each other to form a ring. When R²⁹is a substituent other than the aromatic group, it is preferably a hydrogen atom.

X ¹and X²may the same or different and are each a hydrogen atom, a halogen atom, a hydrocarbon group of 1 to 20 carbon atoms, a halogenated hydrocarbon group of 1 to 20 carbon atoms, an oxygen-containing group or a sulfur-containing group.

Y is a divalent hydrocarbon group of 1 to 20 carbon atoms, a divalent halogenated hydrocarbon group of 1 to 20 carbon atoms, a divalent silicon-containing group, a divalent germanium-containing group, a divalent tin-containing group, —O—, —CO—, —S—, —SO—, —SO ₂—, —NR³⁰P(R³⁰)—, —P(O)(R³⁰)—, —BR³⁰— or —AlR³⁰— (R³⁰is a hydrogen atom, a halogen atom, a hydrocarbon group of 1 to 20 carbon atoms or a halogenated hydrocarbon group of 1 to. 20 carbon atoms).

Examples of the ligands, which contain a monocyclic aromatic ring formed by bonding of at least one combination of “R ²⁶and R²⁷”, “R²⁷and R²⁸” and “R²⁸and R²⁹” and are coordinated to M in the above formula, include ligands represented by the following formulas:

wherein Y is the same as that in the above formula.

Example 4 of the Metallocene Compound

As the metallocene compound, further, a metallocene compound represented by the following formula (5) is also employable.

In the above formula, M, R ²⁴, R²⁵, R²⁶R²⁷R²⁶and R²⁹are the same as those in the formula (4).

Of R ²⁶, R²⁷, R²⁸and R²⁹, two groups including R²⁶are preferably alkyl groups, and R²⁶and R²⁷, or R²⁸and R²⁹are preferably alkyl groups. These alkyl groups are each preferably a secondary or tertiary alkyl group. These alkyl groups may be substituted with a halogen atom or a silicon-containing group, and examples of the halogen atoms and the silicon-containing groups include substituents exemplified for R²⁴and R²⁵.

Of R ²⁶, R²⁷, R²⁸and R²⁹, groups other than the alkyl group are each preferably a hydrogen atom.

Two groups selected from R ²⁶, R²⁷, R²⁸and R²⁹may be bonded to each other to form a monocyclic or polycyclic ring other than an aromatic ring. Examples of the halogen atoms include the same atoms as described with respect to R²⁴and R²⁵.

X ¹, X²and Y are the same as those previously described.

Examples of the metallocene compounds represented by the formula (5) include rac-dimethylsilylene-bis(4,7-dimethyl-1-indenyl)zirconium dichloride, rac-dimethylsilylene-bis(2,4,7-trimethyl-1-indenyl)zirconium dichloride and rac-dimethylsilylene-bis(2,4,6-trimethyl-1-indenyl) zirconium dichloride.

Transition metal compounds wherein the zirconium metal in the above compounds is replaced with a titanium metal or a hafnium metal are also employable. Although the transition metal compound is usually used as racemic modification, it may be used as R form or S form.

Example 5 of the Metallocene Compound

As the metallocene compound, a metallocene compound represented by the following formula (6) is also employable.

In the above formula, M, R ², ⁴, X¹, X²and Y are each the same atom or group as described in the formula (4).

R ²⁴is preferably a hydrocarbon group, particularly preferably an alkyl group of 1 to 4 carbon atoms, such as methyl, ethyl, propyl or butyl.

R ²⁵is an aryl group of 6 to 16 carbon atoms. R²⁵is preferably phenyl or naphthyl. The aryl group may be substituted with a halogen atom, a hydrocarbon group of 1 to 20 carbon atoms or a halogenated hydrocarbon group of 1 to 20 carbon atoms.

X ¹and X²are each preferably a halogen atom or a hydrocarbon group of 1 to 20 carbon atoms.

Examples of the metallocene compounds represented by the formula (6) include rac-dimethylsilylene-bis(4-phenyl-1-indenyl)zirconium dichloride, rac-dimethylsilylene-bis(2-methyl-4-phenyl-1-indenyl)zirconium dichloride, rac-dimethylsilylene-bis(2-methyl-4-((α-naphthyl)-1-indenyl)zirconium dichloride, rac-dimethylsilylene-bis(2-methyl-4-(β-naphthyl)-1-indenyl)zirconium dichloride and rac-dimethylsilylene-bis(2-methyl-4-(l-anthryl)-1-indenyl) zirconium dichloride. Transition metal compounds wherein the zirconium metal in these compounds is replaced with a titanium metal or a hafnium metal are also employable.

Example 6 of the Metallocene Compound

As the metallocene compound, further., a metallocene compound represented by the following formula (7) is also employable.

LaM²X³ ₂ (7)

In the above formula, is a metal of Group 4 or lanthanide series of the periodic table. La is a derivative of a delocalized π bond group and is a group imparting a constrained geometric shape to the metal M ²active site. Each X³may be the same or different and is a hydrogen atom, a halogen atom, a hydrocarbon group containing 20 or less carbon atoms, a silyl group containing 20 or less silicon atoms, or a germyl group containing 20 or less germanium atoms of such compounds, a compound represented by the following formula is preferable.

In the above formula, M ²is titanium, zirconium or hafnium.

X ³is the same as that described in the formula (7).

Cp is π bonded to M ²and is a substituted cyclopentadienyl group having a substituent Z.

Z is oxygen, sulfur, boron or an element of Group 4 of the periodic table, such as silicon, germanium or tin.

Y is a ligand containing phosphorus, oxygen or sulfur, and Z and Y may together form a condensed ring.

Examples of the metallocene compounds represented by the above formula include (dimethyl(t-butylamido) (tetramethyl-η ⁵-cyclopentadienyl)silane)titanium dichloride and ((t-butylamido) (tetramethyl-η⁵-cyclopentadienyl)-1,2-ethanediyl)titanium dichloride. Compounds wherein titanium is replaced with zirconium or hafnium in these metallocene compounds are also employable.

Example 7 of the Metallocene Compound

As the metallocene compound, further, a metallocene compound represented by the following formula (9) is also employable.

In the above formula, M is a transition metal atom of Group 4 of the periodic table, specifically titanium, zirconium or hafnium, preferably zirconium.

Each R ³¹may be the same or different. At least one of R³is an aryl group of 11 to 20 carbon atoms, an arylalkyl group of 12 to 40 carbon atoms, an arylalkenyl group of 13 to 40 carbon atoms, an alkylaryl group of 12 to 40 carbon atoms or a silicon-containing group, or at least two neighboring groups of the groups indicated by R³¹form one or plural aromatic rings or aliphatic rings together with carbon atoms to which they are bonded. In this case, the ring formed by R³¹has, in total, 4 to 20 carbon atoms including carbon atoms to which R³¹is bonded.

R ³¹other than R³¹that forms an aryl group, an arylalkyl group, an arylalkenyl group, an alkylaryl group and an aromatic ring (or aliphatic ring) is a hydrogen atom, a halogen atom, an alkyl group of 1 to 10 carbon atoms or a silicon-containing group.

Each R ³²may be the same or different and is a hydrogen atom, a halogen atom, an alkyl group of 1 to 10 carbon atoms, an aryl group of 6 to 20 carbon atoms, an alkenyl group of 2 to 10 carbon atoms, an arylalkyl group of 7 to 40 carbon atoms, an arylalkenyl group of 8 to 40 carbon atoms, an alkylaryl group of 7 to 40 carbon atoms, a silicon-containing group, an oxygen-containing group, a sulfur-containing group, a nitrogen-containing group or a phosphorus-containing group.

Of the groups indicated by R ³², at least two neighboring groups may form one or plural aromatic rings or aliphatic rings together with carbon atoms to which they are bonded. In this case, the ring formed by R³²has, in total, 4 to 20 carbon atoms including carbon atoms to which R³²is bonded. R³²other than R³²that forms an aromatic ring or an aliphatic ring is a hydrogen atom, a halogen atom, an alkyl group of 1 to 10 carbon atoms or a silicon-containing group.

The group, which is constituted by formation of one or plural aromatic rings or aliphatic rings from two groups indicated by R ³², includes an embodiment wherein the fluorenyl group has the following structure.

R ³²is preferably a hydrogen atom or an alkyl group, particularly preferably a hydrogen atom or a hydrocarbon group of 1 to 3 carbon atoms, such as methyl, ethyl or propyl. A preferred example of the fluorenyl group having such a substituent R³²is a 2,7-dialkyl-fluroenyl group. In this case, the alkyl group of the 2,7-dialkyl is, for example, an alkyl group of 1 to 5 carbon atoms. R³¹and R³²may be the same or different.

R ³³and R³⁴may be the same or different and are each the same hydrogen atom, halogen atom, alkyl group of 1 to 10 carbon atoms, aryl group of 6 to 20 carbon atoms, alkenyl group of 2 to 10 carbon atoms, arylalkyl group of 7 to 40 carbon atoms, arylalkenyl group of 8 to 40 carbon atoms, alkylaryl group of 7 to 40 carbon atoms, silicon-containing group, oxygen-containing group, sulfur-containing group, nitrogen-containing group or phosphorus-containing group as previously described. At least one of R³³and R³⁴is preferably an alkyl group of 1 to 3 carbon atoms.

X ⁴and X⁵are the same or different and are each a hydrogen atom, a halogen atom, a hydrocarbon group of 1 to 20 carbon atoms, a halogenated hydrocarbon group of 1 to 20 carbon atoms, an oxygen-containing group, a sulfur-containing group, a nitrogen-containing group, or a conjugated diene residue formed from X⁴and X⁵.

Preferred examples of the conjugated diene residues formed from X ⁴and X⁵include residues of 1,3-butadiene, 2,4-hexadiene, 1-phenyl-1,3-pentadiene and 1,4-diphenylbutadiene. These residues may be substituted with a hydrocarbon group of 1 to 10 carbon atoms.

X ⁴and X⁵are each preferably a halogen atom, a hydrocarbon group of 1 to 20 carbon atoms or a sulfur-containing group.

Y is a divalent hydrocarbon group of 1 to 20 carbon atoms, a divalent halogenated hydrocarbon group of 1 to 20 carbon atoms, a divalent silicon-containing group, a divalent germanium-containing group, a divalent tin-containing group, —O—, —CO—, —S—, —SO—, SO ₂—, —NR³⁵—, P(R³⁵)—, —P(O)(R³⁵)—, —BR³⁵— or —AlR³⁵— (R³⁵is a hydrogen atom, a halogen atom, a hydrocarbon group of 1 to 20 carbon atoms or a halogenated hydrocarbon group of 1 to 20 carbon atoms).

Of the above divalent groups, preferable is a group wherein the shortest connecting portion of -Y- consists of one or two atoms. R ³⁵is a halogen atom, a hydrocarbon group of 1 to 20 carbon atoms or a halogenated hydrocarbon group of 1 to 20 carbon atoms.

Y is preferably a divalent hydrocarbon group of 1 to 5 carbon atoms, a divalent silicon-containing group or a divalent germanium-containing group, more preferably a divalent silicon-containing group, particularly preferably alkylsilylene, alkylarylsilylene or arylsilylene.

Example 8 of the Metallocene Compound

As the metallocene compound, further, a metallocene compound represented by the following formula (10) is also employable.

Each R ³6 may be the same or different and is a hydrogen atom, a halogen atom, an alkyl group of 1 to 10 carbon atoms, an aryl group of 6 to 10 carbon atoms, an alkenyl group of 2 to 10 carbon atoms, a silicon-containing group, an oxygen-containing group, a sulfur-containing group, a nitrogen-containing group or a phosphorus-containing group. The alkyl group and the alkenyl group may be substituted with a halogen atom.

R ³⁶is preferably an alkyl group, an aryl group or a hydrogen atom, particularly preferably a hydrocarbon group of 1 to 3 carbon atoms, such as methyl, ethyl, n-propyl or i-propyl, an aryl group, such as phenyl, α-naphthyl or β-naphthyl, or a hydrogen atom.

Each R ³⁷may be the same or different and is a hydrogen atom, a halogen atom, an alkyl group of 1 to 10 carbon atoms, an-aryl group of 6 to 20 carbon atoms, an alkenyl group of 2 to 10 carbon atoms, an arylalkyl group of 7 to 40 carbon atoms, an arylalkenyl group of 8 to 40 carbon atoms, an alkylaryl group of 7 to 40 carbon atoms, a silicon-containing group, an oxygen-containing group, a sulfur-containing group, a nitrogen-containing group or a phosphorus-containing group.

The alkyl group, the aryl group, the alkenyl group, the arylalkyl group, the arylalkenyl group and the alkylaryl group may be substituted with halogen.

R ³⁷is preferably a hydrogen atom or an alkyl group, particularly preferably a hydrogen atom or a hydrocarbon group of i-to 4 carbon atoms, such as methyl, ethyl, n-propyl, i-propyl, n-butyl or tert-butyl. R³⁶and R³⁷may be the same or different.

At least one of R ³⁸and R³⁹is an alkyl group of 1 to 5 carbon atoms, and the other is a hydrogen atom, a halogen atom, an alkyl group of 1 to 10 carbon atoms, an alkenyl group or 2 to 10 carbon atoms, a silicon-1.5 containing group, an oxygen-containing group, a sulfur-containing group, a nitrogen-containing group or a phosphorus-containing group.

It is preferable that at least one of R ³8 and R³⁹is an alkyl group of 1 to 3 carbon atoms, such as methyl, ethyl or propyl and the other is a hydrogen atom.

X ⁴and X⁵may be the same or different and are each a hydrogen atom, a halogen atom, a hydrocarbon group of 1 to 20 carbon atoms, a halogenated hydrocarbon group of 1 to 20 carbon atoms, an oxygen-containing group, a sulfur-containing group, a nitrogen-containing group, or a conjugated diene residue formed from X⁴and X⁵. Of these, preferable is a halogen atom or a hydrocarbon group of 1 to 20 carbon atoms.

Y is a divalent hydrocarbon group of 1 to 20 carbon atoms, a divalent halogenated hydrocarbon group of 1 to 20 carbon atoms, a divalent silicon-containing group, a divalent germanium-containing group, a divalent tin-containing group, —O—, —CO—, —S—, —SO—, —SO ₂—, —NR⁴⁰—, —P(R⁴⁰)—, —P(O)(R⁴⁰)—, —BR⁴⁰— or —AlR⁴⁰— (R⁴⁰is a hydrogen atom, a halogen atom, a hydrocarbon group of 1 to 20 carbon atoms or a halogenated hydrocarbon group of 1 to 20 carbon atoms).

The metallocene compounds mentioned above are used singly or in combination of two or more kinds. The metallocene compounds may be diluted with hydrocarbon, halogenated hydrocarbon or the like, prior to use.

Organoaluminum Oxy-Compound

The organoaluminum oxy-compound may be aluminoxane publicly known or may be a benzene-insoluble organoaluminum oxy-compound.

Such publicly known aluminoxane is represented by any one of the following formulas.

In the above formulas, R is a hydrocarbon group, such as methyl, ethyl, propyl or butyl, preferably methyl or ethyl, particularly preferably methyl, and m is an integer of 2 or more, preferably an integer of 5 to 40.

The aluminoxane may be formed from mixed alkyloxyaluminum units consisting of alkyloxyaluminum units represented by the formula (OAl(R)) and alkyloxyaluminum units represented by the formula (OAl(R″)) (R′ and R″ are each the same hydrocarbon group as exemplified for R, and R′ and R″ are groups different from each other). The organoaluminum oxy-compound may contain a small amount of an organic compound of a metal other than aluminum.

Ionizing Ionic Compound

The ionizing ionic compound (sometimes referred to as “ionic ionizing compound” or “ionic compound”) is, for example, Lewis acid, an ionic compound, a borane compound or a carborane compound.

The Lewis acid is, for example, a compound represented by the formula BR ₃(R is a phenyl group, which may have a substituent such as fluorine, methyl or trifluoromethyl, or fluorine). Examples of the Lewis acids include trifluoroboron, triphenylboron, tris(4-fluorophenyl)boron, tris(3,5-difluorophenyl)boron, tris(4′-fluoromethylphenyl)boron, tris(pentafluorophenyl)boron, tris(p-tolyl)boron, tris(o-tolyl)boron and tris(3,5-dimethylphenyl)boron.

The ionic compound is, for example, a trialkyl-substituted ammonium salt, a N,N-dialkylanilinium salt, a dialkylammonium salt or a triarylphosphonium salt. Examples of the trialkyl-substituted ammonium salts as the ionic compounds include triethylammoniumtetra(phenyl)boron, tripropylammoniumtetra(phenyl)boron, tri(n-butyl)ammoniumtetra(phenyl)boron. Examples of the dialkylammonium salts as the ionic compounds include di(l-propyl)ammoniumtetra(pentafluorophenyl)boron and dicyclohexylammoniumtetra(phenyl)boron.

Also available as the ionic compounds are triphenylcarbeniumtetrakis(pentafluorophenyl)borate, N,N-dimethylaniliniumtetrakis(pentafluorophenyl)borate and ferroceniumtetra(pentafluorophenyl)borate.

Examples of the borane compounds include decaborane(9), and salts of metallic borane anions, such as bis[tri(n-butyl)ammonium]nonaborate, bis[tri(n-butyl)ammonium]decaborate and bis[tri(n-butyl)ammonium]bis(dodecahydridododecaborate)niccolate(II I).

Examples of the carborane compounds include 4-carbanonaborane(9), 1,3-dicarbanonaborane(8), and salts of metallic carborane anions, such as bis[tri(n-butyl)ammonium]bis(undecahydrido-7-carbaundecaborate)niccolate(IV).

The ionizing ionic compounds-mentioned above are used singly or in combination of two or more kinds. The organoaluminum oxy-compound and the ionizing ionic compound may be used in the supported form on the aforesaid carrier compounds.

In the preparation of the metallocene catalyst, the following organoaluminum compound may be used together with the organoaluminum oxy-compound and/or the ionizing ionic compound.

Organoaluminum Compound

As the organoaluminum compound that is used when needed, a compound having at least one Al-carbon bond in the molecule is employable. Examples of such compounds include:

an organoaluminum compound represented by the following formula (11):

(R⁴¹)_mAl(OR⁴²)_nH_pX⁶ _q (11)

wherein R ⁴¹and R⁴²may the same or different and are each a hydrocarbon group of usually 1 to 15 carbon atoms, preferably 1 to 4 carbon atoms, X⁶is a halogen atom, and m, n, p and q are numbers satisfying conditions of 0<m≦3, 0≦n<3, 0≦p<3, 0≦q<3 and m+n+p+q=3; and

an alkyl complex compound of a Group 1 metal and aluminum, which is represented by the following formula (12):

(M³)Al(R⁴¹) (12)

wherein M ³is Li, Na or K, and R⁴¹is the same as R⁴¹in the formula (11).

Polymerization

The ethylene/α-olefin random copolymer for use in the invention can be prepared by, for example, copolymerizing ethylene and an α-olefin of 3 to 20 carbon atoms in the presence of the above-mentioned metallocene catalyst usually in a liquid phase. Although a hydrocarbon solvent is generally used as a polymerization solvent, an α-olefin may be used as the solvent. The monomers used herein are those previously described.

The copolymerization reaction may be carried out batchwise or continuously. When the copolymerization is carried out batchwise, the aforesaid catalyst components are used in the following concentrations.

The concentration of the metallocene compound in the polymerization system is in the range of usually 0.00005 to 0.1 mmol/l (polymerization volume), preferably 0.0001 to 0.05 mmol/l. The organoaluminum oxy-compound is fed in such an amount that the molar ratio (Al/transition metal) of the aluminum atom to the transition metal in the metallocene compound in the polymerization system becomes 1 to 10000, preferably 10 to 5000.

The ionizing ionic compound is fed in such an amount that the molar ratio (ionizing ionic compound/metallocene compound) of the ionizing ionic compound to the metallocene compound in the polymerization system becomes 0.5 to 20, preferably 1 to 10.

The organoaluminum compound is used in an amount of usually about 0 to 5 mmol/l (polymerization volume), preferably about 0 to 2 mmol/l.

The copolymerization reaction is carried out under the conditions of a temperature of usually −20 to +150° C., preferably 0 to-120° C., more preferably 0 to 100° C., and a pressure of more than 0 MPa and not more than 7.8 MPa (80 kgf/cm ², gauge pressure), preferably more than 0 MPa and not more than 4.9 MPa (50 kgf/cm², gauge pressure).

In the copolymerization, ethylene and the α-olefin of 10 to 20 carbon atoms are fed in such amounts that an ethylene/α-olefin random copolymer of the aforesaid specific composition is obtained. In the copolymerization, further, a molecular weight modifier such as hydrogen may be added.

Lubricating Oil Composition

The lubricating oil composition of the invention comprises:

(A) at least one base oil selected from a synthetic hydrocarbon, a mineral oil and an ester, which has a kinematic viscosity at 100° C. of 1 to 20 mm 2/s,

(B) the aforesaid ethylene/α-olefin random copolymer,

and optionally,

(C) at least one additive selected from the group consisting of a dispersant, a viscosity index improver, an antioxidant, a corrosion inhibitor, an anti-wear agent, a pour point depressant., a rust preventive, an anti-foaming agent and an extreme pressure agent.

Base Oil

The base oil used in the lubricating oil composition of the invention has a kinematic viscosity at 100° C. of 1 to 20 mm ²/s and is selected from a synthetic hydrocarbon, a mineral oil and an ester. As the synthetic hydrocarbon, the mineral oil and the ester, those conventionally known are employed.

Examples of the synthetic hydrocarbons having a kinematic viscosity at 100° C. of 1 to 20 mm ²/s include α-olefin oligomers, alkylbenzenes and alkylnaphthalenes. These can be used singly or in combination of two or more kinds. As the α-olefin oligomer, a low-molecular weight oligomer of at least one olefin selected from olefins of 8 to 12 carbon atoms is employable. The α-olefin oligomer can be prepared by polymerization using a Ziegler catalyst, thermal polymerization, polymerization using free radical as a catalyst, or polymerization using BF₃as a catalyst. Such polymerization processes are described in, for example, U.S. Pat. No. 4,045,508.

Most of the alkylbenzenes or the alkylnaphtnalenes employable as the base oil are usually dialkylbenzenes or dialkylnaphthalenes wherein the alkyl chains have 6 to 14 carbon atoms, and such dialkylbenzenes or alkylnaphthalenes are prepared by Friedel-Crafts alkylation of benzene or naphthalene and olefin. The alkylation olefin used in the preparation of the alkylbenzenes or the alkylnaphthalenes may be a linear olefin, a branched olefin or a combination thereof. The process for preparing them is described in, for example, U.S. Pat. No. 3,909,432.

Examples of the esters having a kinematic viscosity at 100° C. of 1 to 20 mm ²/s include monoesters prepared from monobasic acids such as pelargonic acid and alcohols; diesters prepared from dibasic acids and alcohols or prepared from diols and monobasic acids or acid mixtures; and polyol esters prepared by the reaction of diols, triols (e.g., trimethylolpropane), tetraols (e.g., pentaerythritol) or hexaols (e.g., dipentaerythritol) with monobasic acids or acid mixtures. Particular examples of such esters include tridecyl pelargonate, di-2-ethylhexyl adipate, di-2-ethylhexyl azelate, trimethylolpropane triheptanoate and pentaerythritol tetraheptanoate.

Other Additives

Examples of other additives, which can be added to the lubricating oil composition of the invention when needed, include:

detergents, such as neutral or basic sulfonates and phenates (metal salt type);

dispersants, such as succinimide, esters, benzylamine and copolymerization type polymers (ashless type);

pour point depressants, such as condensates of chlorinated paraffin and naphthalene or phenol, polyalkyl acrylates, polyalkyl methacrylates, polybutene, polyalkylstyrene and polyvinyl acetate;

antioxidants, such as zinc thiophosphate and trialkylphenol;

viscosity index improvers, such as high-molecular weight ethylene/propylene copolymer and PMA;

emulsifying agents, such as sulfuric ester, sulfonic ester, phosphoric ester, fatty acid derivatives, amine derivatives, quaternary ammonium salt and polyoxyethylene type activators;

demulsifying agents, such as quaternary ammonium salt, sulfonated oil and phosphoric ester;

antifungal substances, such as phenolic compounds, formaldehyde donative compounds and salicylanilide type compounds;

anti-stain agents;

untoucher agents;

anti-scorching agents; and

extreme pressure agents.

Composition

In the lubricating oil composition of the invention, the content of the component (A) is in the range of 50 to 99.8 parts by weight, preferably 60 to 95 parts by weight, and the content of the component (B) is in the range of 0.2 to 50 parts by weight, preferably 5 to 40 parts by weight, with the proviso that the total of the component 0.20 (A) and the component (B) is 100 parts by weight. The compounding ratio between the component (A) and the component (B) is so determined that the resulting composition has a kinematic viscosity of a prescribed value.

When the contents of the component (A) and the component (B) are in the above ranges, an economical lubricating oil composition having excellent shear stability, high viscosity index and low low-temperature viscosity can be obtained.

The lubricating oil composition of the invention has high viscosity index and shear stability and also has good appearance without turbidity.

EFFECT OF THE INVENTION

The lubricating oil thickening agent according to the invention has high viscosity index improvability and shear stability.

The lubricating oil composition according to the invention exhibits high viscosity index and shear stability and has good appearance without turbidity.

EXAMPLE

The present invention is further described with reference to the following examples, but it should be construed that the invention is in no way limited to those examples. [0212]
The methods for evaluating the examples are as follows. [0213]
Kinematic Viscosity (mm[0214] ²/s)
The kinematic viscosity was measured in accordance with JIS K 2283. [0215]
Viscosity Index [0216]
The viscosity index was measured in accordance with JIS K 2283. [0217]
Intrinsic Viscosity [η] (di/g) [0218]
The intrinsic viscosity was measured in decalin at 135° C. [0219]
Number-Average Molecular Weight, Mw/Mn [0220]
The number-average molecular weight and Mw/Mn were measured by GPC using polystyrene as a molecular weight standard substance. [0221]
KRL shear stability (%) [0222]
A decrease (%) of the kinematic viscosity at 100° C. was measured in accordance with the CEC test method under the conditions of 20 hours. [0223]
Pour point (°C.) [0224]
The pour point was measured in accordance with JIS K 2269. [0225]
Low-temperature viscosity (mPa·s) [0226]
The viscosity at −26° C. was measured in accordance with ASTM D 2983. [0227]
Appearance [0228]
The appearance was visually observed, and a lubricating oil composition free from turbidity was evaluated as good. [0229]
In the examples and the comparative examples, the following copolymers were used. [0230]
Ethylene/1-decence copolymer (1) [0231]
ethylene content: 57% by mol, kinematic viscosity (100° C.): 361 mm[0232] ²/S, [η]: 0.120 dl/g, Mn: 8,600, Mw/Mn: 1.7
Ethylene/1-decence copolymer (2) [0233]
ethylene content: 60% by mol, kinematic viscosity (100° C.): 730 mm[0234] ²/S, [η]: 0.165 dl/g, Mn: 10,700, Mw/Mn: 1.6
Ethylene/1-decence copolymer (3) [0235]
ethylene content: 60% by mol, kinematic viscosity (100° C.): 1,440 mm[0236] ²/s, [η]: 0.190 dl/g, Mn: 13,400, Mw/Mn: 1.8
Ethylene/1-decence copolymer (4) [0237]
ethylene content: 66% by mol, kinematic viscosity (100° C.): 15,600 mm[0238] ²/S, [η]: 0.375 dl/g, Mn: 26,400, Mw/Mn: 1.8
Ethylene/1-octene copolymer (5) [0239]
ethylene content: 60% by mol, kinematic viscosity (100° C.): 1,460 mm[0240] ²/s, [η]: 0.180 dl/g, Mn: 10,600, Mw/Mn: 1.6
Ethylene/propylene/1-decence copolymer (6) [0241]
ethylene content: 65% by mol, propylene content: 5% by mol, 1-decene content: 30% by mol, kinematic viscosity (100° C.): 3,030 mm[0242] ²/s, [η]: 0.240 dl/g, Mn: 16,100, Mw/Mn: 1.7
Ethylene/1-dodecene/1-tetradecence copolymer (7) [0243]
ethylene content: 65% by mol, 1-dodecene content: 20% by mol, 1-tetradecene content: 15% by mol, kinematic viscosity (100° C.): 1,400 mm[0244] ²/s, [η]: 0.235 dl/g, Mn: 24,700, Mw/Mn: 1.6
Ethylene/propylene copolymer (8) [0245]
ethylene content: 50% by mol, kinematic viscosity (100° C.): 600 mm[0246] ²/s, [η]: 0.140 dl/g, Mn: 5,220, Mw/Mn: 1.8.
Ethylene/propylene copolymer (9) [0247]
ethylene content: 50% by mol, kinematic viscosity (100° C.): 2,000 mm[0248] ²/s, [η]: 0.190 dl/g, Mn: 7,730, Mw/Mn: 1.8
Ethylene/propylene copolymer (10) [0249]
ethylene content: 50% by mol, kinematic viscosity (100° C.): 15,600 mm[0250] ²/s [η]: 0.353 dl/g, Mn: 15,000, Mw/Mn: 1.9
Ethylene/1-decence copolymer-(11) [0251]
ethylene content: 65% by mol, [η]: 0.50 dl/g, Mn: 52,000, Mw/Mn: 1.6 [0252]
Ethylene/propylene/1-decence copolymer (12) [0253]
ethylene content: 65% by mol, propylene content: 15% by mol, 1-decene content: 20% by mol, [η]: 0.170 dl/g, Mn: 11,500, kinematic viscosity (100° C.): 933 mm[0254] ²/s, Mw/Mn: 1.6
Ethylene/propylene/1-decence-copolymer (13) [0255]
ethylene content: 65% by mol, propylene content: 15% by mol, 1-decene content: 20% by mol, [η]: 0.240 dl/g, Mn: 16,100, kinematic viscosity (100° C.): 3,030 mm[0256] ²/s, Mw/Mn: 1.7
Ethylene/1-butene/1-decence copolymer (14) [0257]
ethylene content: 50% by mol, 1-butene content: 15% by mol. 1-decene content: 35% by mol, [η]: 0.202 dl/g, Mn: 14,400, kinematic viscosity (100° C.): 2,000 mm[0258] ²/s, Mw/Mn: 1.7.
Ethylene/propylene/1-dodecence copolymer (15) [0259]
ethylene content: 65% by mol, propylene content: 15% by mol, 1-dodecene content: 20% by mol, [η]: 0.220 dl/g, Mn: 16,000, kinematic viscosity (100° C.): 2,000 mm[0260] ²/s, Mw/Mn: 1.7
Ethylene/propylene/1-decence copolymer (16) [0261]
ethylene content: 15% by mol, propylene content: 15% by mol, 1-decene content: 70% by mol, [η]: 0.240 dl/g, Mn: 17,500, kinematic viscosity (100° C.): 4,000 mm[0262] ²/s, Mw/Mn: 1.8
Ethylene/propylene copolymer (17) [0263]
ethylene content: 50% by mol, propylene content: 50% by mol, [η]: 0.190 dl/g, Mn: 7,700, kinematic viscosity (100° C.): 2,000 mm[0264] ²/S, Mw/Mn: 1.9
Ethylene/1-decene copolymer (18) [0265]
ethylene content: 10% by mol, 1-decene content: 90% by mol, [η]: 0.200 dl/g, Mn: 16,500, kinematic viscosity (100° C.): 2,300 mm[0266] ²/s, Mw/Mn: 2.0
Ethylene/propylene/1-decence copolymer (19) [0267]
ethylene content: 80% by mol, propylene content: 5% by mol, 1-decene content: 10% by mol, [η]: 0.205 dl/g, Mn: 35,000, kinematic viscosity (100° C.): 2,100 mm[0268] ²/s, Mw/Mn: 1.8
In the evaluations of the examples and the comparative examples, the following base oil and additives were used. [0269]
Mineral oil (100N) [0270]
available from Fuji Kosan K.K., F-NT100 (100° C. kinematic viscosity: 4.29 mm[0271] ²/S, viscosity index: 100)
Pour point depressant [0272]
available from Sanyo Kasei Kogyo K.K., ACLUBE 136, amount added: 0.5% [0273]
Extreme pressure agent [0274]
available from Lubrizol, ANGRAMOL 98A, amount added: 6.5% [0275]

Examples 1 to 12, Comparative Examples 1 to 7

The components shown in Tables 1 to 4 were mixed in the formulations (unit: g) shown in Tables 1 to 4 at 100° C. for 1 hour, to obtain lubricating oil compositions. Evaluation results of properties of the compositions are set forth in Tables 1 to 4.

TABLE 1


Formulation	Ex. 1	Ex. 2	Ex. 3	Ex. 4	Ex. 5	Ex. 6	Ex. 7

Ethylene/1-decene copolymer (1)	18.6
Ethylene/1-decene copolymer (2)		14.5
Ethylene/1-decene copolymer (3)			12.4
Ethylene/1-decene copolymei (4)				6.7
Ethylene/1-octene copolymer (5)					12.5
Ethylene/propylene/1-decene copolymer (6)						10.0
Ethylene/1-dodecene/1-tetradecene copolymer (7)							10.5
Pour point depressant	0.5	0.5	0.5	0.5	0.5	0.5	0.5
Extreme pressure agent	6.5	6.5	6.5	6.5	6.5	6.5	6.5
Mineral oil (100 N)	74.4	78.5	80.6	86.3	80.5	83.0	82.5
Compounded oil properties
Kinematic viscosity (mm²/s, at 40° C.)	85.4	85.9	85.6	83.4	88.1	84.9	79.5
Kinematic viscosity (mm²/s, at 100° C.)	14.0	14.0	14.1	14.2	14.1	13.99	13.85
Viscosity index	168	168	171	177	165	170	180
Low-temperature viscosity (mPa · s, at -	9,950	11,000	13,200	10,600	12,300	12,000	7,980
26° C.)
Shear stability (viscosity decrease, %)	7.1	14.1	20.9	29.1	13.6	23.6	27.8
Appearance	good	good	good	good	good	good	good

TABLE 2


	Comp.	Comp.	Comp.	Comp.
Formulation	Ex. 1	Ex. 2	Ex. 3	Ex. 4

Ethylene/propylene copolymer (8)	16.0
Ethylene/propylene copolymer (9)		11.8
Ethylene/propylene copolymer (10)			6.6
Ethylene/1-decene copolymer (11)				5.0
Pour paint depressant	0.5	0.5	0.5	0.5
Extreme pressure agent	6.5	6.5	6.5	6.5
Mineral oil (100 N)	77.0	81.2	86.4	88.0
Compounded oil properties
Kinematic viscosity (mm²/s,	93.7	94.3	91.9	78.0
at 40° C.)
Kinematic viscosity (mm²/s,	14.0	14.3	14.2	13.8
at 100° C.)
Viscosity index	152	157	159	183
Low-temperature viscosity	13,200	15,600	14,700	7,980
(mPa · s, at −26° C.)
Shear stability (viscosity decrease,	3.8	9.2	26.3	49.0
%)
Appearance	good	good	good	good

TABLE 3


Formulation	Ex. 8	Ex. 9	Ex. 10	Ex. 11	Ex. 12

Ethylene/propylene/1-decene copolymer (12)	13.8
Ethylene/propylene/1-decene copolymer (13)		11.5
Ethylene/1-butene/1-decene copolymer (14)			11.2
Ethylene/propylene/1-dodecene copolymer				11.0
(15)
Ethylene/propylene/1-decene copolymer (16)					10.1
PMA	0.5	0.5	0.5	0.5	0.5
Extreme pressure agent	6.5	6.5	6.5	6.5	6.5
Mineral oil (100 N)	79.2	83.0	81.8	82.0	82.9
Compounded oil properties
Kinematic viscosity (mm²/s, at 40° C.)	86.93	84.87	83.36	82.90	82.92
Kinematic viscosity (mm²/s, at 100° C.)	14.01	13.99	13.90	13.84	13.96
Viscosity index	166	170	172	172	174
Shear stability (viscosity decrease, %)	9.1	10.6	12.8	10.1	20.5
Pour point (° C.)	−42.5	−42.5	−42.5	−40	−42.5

TABLE 4


	Comp.	Comp.	Comp.
Formulation	Ex. 5	Ex. 6	Ex. 7

Ethylene/propylene copolymer (17)	11.8
Ethylene/1-decene copolymer (18)		12.0
Ethylene/propylene/1-decene copolymer (19)			11.4
PMA (pour point depressant)	0.5	0.5	0.5
Extreme pressure agent	6.5	6.5	6.5
Mineral oil (100 N)	81.2	81.0	81.6
Compounded oil properties
Kinematic viscosity (mm²/s, at 40° C.)	91.02		84.90
Kinematic viscosity (mm²/s, at 100° C.)	14.01		13.83
Viscosity index	158	165	167
Shear stability (viscosity decrease, %)	9.2	32.1	9.0
Pour point (° C.)	−37.5	−35	−5

Claims

What is claimed is:

1. A lubricating oil additive comprising an ethylene/α-olefin random copolymer having the following properties:

(ii) the kinematic viscosity at 100° C. is in the range of 500 to 1,000,000 mm²/s,

(iv) the molecular weight distribution (Mw/Mn, Mw:

weight-average molecular weight, Mn: number-average molecular weight), as measured by gel permeation chromatography, is not more than 4, and

(v) the number-average molecular weight is in the range of 5,000 to 30,000.

2. The lubricating oil additive as claimed in claim 1, wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 30 to 75% by mol and constituent units derived from at least one α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 25 to 70% by mol.

3. The lubricating oil additive as claimed in claim 1, wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 30 to 75% by mol and constituent units derived from at least one α-olefin selected from α-olefins of 10 to 16 carbon atoms in amounts of 25 to 70% by mol.

4. The lubricating oil additive as claimed in claim 1, wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 35 to 70% by mol and constituent units derived from 1-decene in amounts of 30 to 65% by mol.

5. The lubricating oil additive as claimed in claim 1, wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 10 to 75% by mol., constituent units derived from at least one lower α-olefin selected from α-olefins of 3 to 6 carbon atoms in amounts of 5 to 50% by mol, and constituent units derived from at least one higher α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 20 to 85% by mol.

6. The lubricating oil additive as claimed in claim 1, wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 10 to 70% by mol, constituent units derived from at least one lower α-olefin selected from α-olefins of 3 to 6 carbon atoms in amounts of 10 to 40% by mol, and constituent units derived from at least one higher α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 20 to 80% by mol.

7. The lubricating oil additive as claimed in claim 1, wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 10 to 70% by mol, constituent units derived from at least one lower α-olefin selected from α-olefins of 3 to 4 carbon atoms in amounts of 10 to 40% by mol, and constituent units derived from at least one higher α-olefin selected from α-olefins of 10 to 14 carbon atoms in amounts of 20 to 80% by mol.

8. The lubricating oil additive as claimed in claim 1, wherein the ethylene/α-olefin random copolymer contains constituent units derived from ethylene in amounts of 10 to 70% by mol, constituent units derived from propylene in amounts of 10 to 40% by mol, and constituent units derived from 1-decene in amounts of 20 to 80% by mol.

9. A lubricating oil additive containing constituent units derived from ethylene in amounts of 30 to 75% by mol and constituent units derived from at least one α-olefin selected from α-olefins of 8 to 20 carbon atoms in amounts of 25 to 70% by mol, and having the following properties:

B≧0.4×A+155,

and

A is a number satisfying the condition of A≦30.

10. The lubricating oil additive as claimed in claim 9, wherein the shear stability (A (%)) and the low-temperature viscosity (C (mPa·s)) as measured at −26° C. satisfy the following formula:

C≦−50×A+15,000.

11. A lubricating oil composition comprising:

(A) at least one base oil selected from a synthetic hydrocarbon, a mineral oil and an ester, which has a kinematic viscosity at 100° C. of 1 to 20 mm²/s, in an amount of 50 to 99.8 parts by weight,

(B) the lubricating oil additive of-any one of claims 1 to 10, in an amount of 0.2 to 50 parts by weight, with the proviso that the total of the component (A) and the component (B) is 100 parts by weight, and optionally,