[Technical Field]
[0001] The present invention relates to lubricating oil compositions for internal combustion
engines and particularly to those having excellent anti-wear properties, base number
retaining properties, high-temperature detergency, and low friction characteristics.
[Background Art]
[0002] Zinc dialkyldithiophosphates (ZDTP) have excellent anti-wear properties and anti-oxidation
properties as a peroxide decomposer and thus have been used as an essential additive
in lubricating oils for internal combustion engines or in every sort of lubricating
oils.
[0003] On the other hand, lubricating oil compositions blended with zinc dialkyldithiocarbamates
and sulfur-based additives so as to retain the anti-wear properties are known as ZDTP-free
lubricating oils as disclosed in Japanese Patent Laid-Open Publication Nos. 52-704,
62-253691, 63-304095, and 6-41568 and Published Japanese Translation Nos. 62-501572,
62-501917, and 1-500912. The lubricating oils disclosed in these publications contain
a large quantity of sulfur similarly to those containing ZDTP. Such lubricating oils
are poor in oxidation stability and tend to be acceleratingly decreased in base number.
[0004] After an extensive research and study, focusing on the ability to retain the base
number of lubricating oils for internal combustion engine containing a large amount
of sulfur, it was found that a compound containing sulfur such as ZDTP itself generates
sulfuric acid in the lubricating oil when oxidized or thermally decomposed, and thus
the lubricating oil containing such a compound is exhausted in base number, leading
to a shortened working life, significantly deteriorated in detergency particularly
at high temperature, and poor in low friction characteristics.
[0005] It was also found that when a deeply-desulfurized gas oil decreased in sulfur content
to 50 ppm by mass or less, for a diesel engine equipped with DPF (diesel particulate
filter); kerosene, gasoline, LPG, or natural gas, containing 50 ppm by mass or less
of sulfur; or hydrogen, dimethylether, or alcohol, containing no sulfur is used as
fuel, a lubricating engine oil is decreased in sulfuric acid contamination caused
by sulfur in the fuel and thus prolonged in working life, compared with the case using
a high sulfur content fuel. However, the use of such a low sulfur content fuel is
too insufficient to provide an engine oil, with a longer drain-interval and further
enhance high-temperature detergency. Therefore, it is now necessary to study on an
additive taking the place of various sulfur-containing anti-wear agents and anti-oxidants.
Particularly, since gas engines are generally high in combustion temperaturer the
lubricating oil used therefor is exposed to high temperature or NOx and thus required
to be improved in oxidation stability or high-temperature detergency. Furthermore,
in order to maintain the performances of exhaust gas purifying systems such as DPF,
ternary catalysts, oxidation catalysts, NOx adsorber catalysts, and EGR (exhaust gas
recirculation) device, an engine oil is desired to be less in sulfur content.
[0006] Therefore, the object of the present invention is to provide a lubricating oil composition
for internal combustion engines, which composition retains or is improved in anti-wear
properties and anti-oxidation properties as obtained by conventional ZDTP; is enhanced
in long-drain properties by decreasing the sulfur content of the oil so as to suppress
the exhaust of the base number caused by deterioration of the oil; and is also excellent
in high-temperature detergency and low friction characteristics. [Disclosures of the
Invention)
[0007] As a result of an extensive research and study, the present invention was completed
based on the finding that a lubricating oil which is excellent in anti-wear properties,
high-temperature detergency, and low friction characteristics and improved in base
number retaining properties leading to long drain properties can be obtained by blending
a lubricating base oil with a specific phosphorus compound, a specific ashless dispersant,
a specific metal detergent, and a specific anti-oxidant, in a specific amount, respectively.
[0008] That is, according to the present invention, there is provided, a lubricating oil
composition for internal combustion engine, comprising a lubricating base oil; (A)
a triphosphate represented by formula (1) below in an amount of 0.01 to 0.2 percent
by mass in terms of phosphorus; (B) succinimide and/or derivative thereof in an amount
of 0.01 to 0.3 percent by mass in terms of nitrogen; (C) an alkali metal or alkaline
earth metal detergent in an amount of 0.05 to 1 percent by mass in terms of metal;
and (D) a phenol-based and/or amine-based anti-oxidants in an amount of 0.01 to 3
percent by mass:
O = P(OR
1)
3 (1)
wherein the groups R
1 are each independently a hydrocarbon group having 1 to 30 carbon atoms and may be
the same or different from each other.
[0009] In the lubricating oil composition of the present invention, the alkali metal or
alkaline earth metal detergent preferably contains an alkali metal or alkaline earth
metal salicylate detergent.
[0010] In the lubricating oil composition of the present invention, the alkali metal or
alkaline earth metal detergent is preferably an alkali metal or alkaline earth metal
salicylate detergent whose metal ratio represented by "valence of metal element x
metal element content (mol) / soap group content (mol)" is 3 or less.
[0011] In the lubricating oil composition of the present invention, the alkali metal or
alkaline earth metal detergent is preferably a mixture of an alkali metal or alkaline
earth metal salicylate detergent whose metal ratio represented by "valence of metal
element x metal element content (mol) / soap group content (mol)'' is 1.5 or less
and an alkali metal or alkaline earth metal salicylate detergent whose metal ratio
is more than 1.5.
[0012] In the lubricating oil composition of the present invention, the alkali metal or
alkaline earth metal detergent is preferably a mixture of an alkali metal or alkaline
earth metal salicylate detergent whose metal ratio represented by "valence of metal
element x metal element content (mol) / soap group content (mol)" is 1.5 or less and
an alkali metal or alkaline earth metal sulfonate detergent.
[0013] The lubricating oil composition of the present invention preferably contains a sulfur-containing
anti-wear agent in an amount of 0.1 percent by mass or less in terms of sulfur.
[0014] The lubricating oil composition of the present invention preferably contains a lubricating
base oil whose aromatic content is 3 percent by mass or less and sulfur content is
50 ppm by mass or less.
[0015] The lubricating oil composition of the present invention is preferably used in an
internal combustion engine using a fuel whose sulfur content is 50 ppm by mass or
less.
[0016] The lubricating oil composition of the present invention is preferably used in gas
engines.
[0017] The lubricating base oil of the lubricating oil composition of the present invention
may be any of conventional mineral oils, synthetic oils, or mixtures of two or more
of these oils mixed at an arbitrary ratio. For example, the mixture may be those of
one or more types of mineral lubricating oils, those of one or more types of synthetic
lubricating oils, or those of one or more types of mineral lubricating oils and one
or more types of synthetic lubricating oils.
[0018] Specific examples of mineral lubricating oils are paraffinic or naphthenic oils which
can be obtained by subjecting a lubricating oil fraction produced by atmospheric-
or vacuum-distilling a crude oil, to any one or more refining processes selected from
solvent deasphalting, solvent extraction, hydrocracking, solvent dewaxing, catalytic
dewaxing, hydrorefining, washing with sulfuric acid, and clay treatment; and n-paraffines.
Particularly, preferred are those obtained by a high-degree hydrocracking process
or those obtained by isomerizing GTL Wax (Gas To Liquid Wax), both of which methods
are capable of further decreasing the aromatic content and sulfur content.
[0019] No particular limitation is imposed on synthetic lubricating oils. Examples of synthetic
lubricating oils include poly-α-olefins such as 1-octene oligomer, 1-decene oligomer,
and ethylene-propylene oligomer, and hydrides thereof; isobutene oligomer and hydrides
thereof; isoparaffines; alkylbenzenes; alkylnaphthalenes; diesters such as ditridecyl
glutarate, di-2-ethylhexyl adipate, diisodecyl adipate, ditridecyl adipate, and di-2-ethylhexyl
cebacate; polyol esters such as trimethylolpropane caprylate, trimethylolpropane pelargonate,
pentaerythritol-2-ethyl hexanoate, and pentaerythritol pelargonate; polyoxyalkylene
glycols; dialkyldiphenyl ethers; and polyphenyl ethers.
[0020] No particular limitation is imposed on the sulfur content of the lubricating base
oil. However, the sulfur content of the base lubricating oil is preferably 500 ppm
by mass or less, more preferably 50 ppm by mass or less, even more preferably 20 ppm
by mass or less, and particularly preferably 10 ppm by mass or less. A lubricating
base oil containing too much sulfur would adversely affect the base number retaining
properties of the resulting composition and the above-described exhaust gas purifying
systems.
[0021] Although no particular limitation is imposed on the total aromatic content of the
lubricating base oil, it is preferably 15 percent by mass or less, more preferably
10 percent by mass or less, and even more preferably 3 percent by mass or less, and
particularly preferably 2 percent by mass of less. A lubricating base oil whose total
aromatic content is more than 15 percent by mass would be poor in base number retaining
properties and high-temperature detergency. The term "total aromatic content" used
herein denotes an aromatic fraction content determined in accordance with ASTM D2549.
The aromatic fraction includes alkylbenzenes; alkylnaphthalens; anthracene, phenanthrene,
and alkylated products thereof; compounds wherein four or more benzene rings are condensated
to each other; and compounds having heteroaromatics such as pyridines, quinolines,
phenols, and naphthols.
[0022] No particular limitation is imposed on the kinematic viscosity at 100 °C of the lubricating
base oil. However, the kinematic viscosity at 100 °C is preferably 1 to 20 mm
2/s and particularly preferably 2 to 10 mm
2/s in order to improve low-temperature viscosity characteristics and oil film formation
capability at lubricated sites and reduce the evaporation loss of the lubricating
base oil.
[0023] No particular limitation is imposed on the viscosity index of the lubricating base
oil. However, the viscosity index is preferably 80 or higher, more preferably 100
or higher, and further more preferably 120 or higher.
[0024] Component (A) of the lubricating oil composition of the present invention is a triphosphate
represented by the formula
O = P(OR
1)
3 (1)
[0025] In formula (1), R
1 is a hydrocarbon group having 1 to 30 carbon atoms. Three groups of R
1 may be the same or different from each other.
[0026] Examples of the hydrocarbon group having 1 to 30 carbon atoms are alkyl, cycloalkyl,
alkenyl, aryl, and arylalkyl groups.
[0027] Examples of the alkyl group include straight-chain or branched alkyl groups such
as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl,
dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, and octadecyl groups.
[0028] The cycloalkyl group may have a substituent. Examples of the cycloalkyl group include
those having 5 to 7 carbon atoms, such as cyclopentyl, cyclohexyl, and cycloheptyl
groups; and alkylcycloalkyl groups having 6 to 11 carbon groups, such as methylcyclopentyl,
dimethylcyclopentyl, methylethylcyclopentyl, diethylcyclopentyl, methylcyclohexyl,
dimethylcyclohexyl, methylethylcyclohexyl, diethylcyclohexyl, methylcycloheptyl, dimethylcycloheptyl,
methylethylcycloheptyl, and diethylcycloheptyl groups, of which the alkyl groups may
bond to any position of the cycloalkyl groups.
[0029] Examples of the alkenyl group include those having 2 to 30 carbon atoms, such as
butenyl, pentenyl, hexenyl, heptenyl, octenyl, noneyl, decenyl, undecenyl, dodecenyl,
tridecenyl, tetradecenyl, pentadecenyl, hexadecenyl, heptadecenyl, and octadecenyl
groups, all of which may be straight-chain or branched and the position of which the
double bonds may vary.
[0030] The aryl group may be substituted by an alkyl group. Examples of the aryl group include
those having 6 to 18 carbon atoms, such as phenyl and naphtyl groups; and alkylaryl
groups having 7 to 26 carbon atoms, such as tolyl, xylyl, ethylphenyl, propylphenyl,
butylphenyl, pentylphenyl, hexylphenyl, heptylphenyl, octylphenyl, nonylphenyl, decylphenyl,
undecylphenyl, dodecylphenyl, diethylphenyl, dibutylphenyl, and dioctylphenyl groups,
wherein the alkyl groups may be straight-chain or branched and the position thereof
to the aryl group may vary.
[0031] Examples of the arylalkyl groups include those having 7 to 12 carbon atoms, such
as benzyl, phenylethyl, phenylpropyl, phenylbutyl, phenylpentyl, and phenylhexyl groups,
of which the alkyl groups may be straight-chain or branched.
[0032] The hydrocarbon group of R
1 is preferably a straight-chain or branched alkyl group having 3 to 18 carbon atoms,
an aryl having 6 to 18 carbon atoms, or a straight-chain or branched alkylaryl group
having 7 to 26 carbon atoms, more preferably an alkyl group having 3 to 5 carbon atoms
with the objective of excellent base number regaining properties, and is also preferably
a straight-chain or branched alkyl group having 6 to 18 carbon atoms, an aryl having
6 to 10 carbon atoms, or a straight-chain or branched alkylaryl group having 7 to
10 carbon atoms with the objective of high-temperature detergency. In the present
invention, R
1 is desirously a straight-chain or branched alkyl group having 6 to 18, preferably
6 to 12 carbon groups because the resulting composition would be low in volatility
and excellent in high temperature detergency and friction-reducing effect. All the
groups of R
1 are preferably the same.
[0033] The use of a triphosphate represented by formula (1) can decrease the metal content
of the resulting composition compared with the use of a metal anti-wear agent such
as ZDTP and can obtain a lubricating oil composition with more enhanced anti-wear
properties, base number retaining properties, and high-temperature detergency, compared
with the use of ZDTP, monophosphates, diesters, or phosphites.
[0034] The lower limit content of Component (A) is 0.01 percent by mass, preferably 0.02
percent by mass, and particularly preferably 0.05 percent by mass in terms of phosphorus,
based on the total mass of the composition, while the upper limit content of Component
(A) is 0.2 percent by mass, preferably 0.15 percent by mass, and particularly preferably
0.1 percent by mass in terms of phosphorus, based on the total mass of the composition.
Component (A) of less than 0.01 percent by mass would fail to obtain advantageous
effects of the present invention sufficiently, while Component (A) of more than 0,2
percent by mass would adversely affect exhaust gas purifying catalysts or the like.
[0035] Component (B) of the lubricating oil composition of the present invention is a succinimide
and/or derivative thereof.
[0036] Examples of succinimide are monosuccinimides represented by formula (2) below and
bissuccinimides represented by formula (3) below:

[0037] In formulas (2) and (3), R
10, R
11, and R
12 are each independently a polybutenyl group and n is an integer of from 2 to 7. In
the present invention, preferred are bis-type succinimides represented by formula
(3) because they can further enhance the advantageous effects achieved by the present
invention.
[0038] The polybutenyl group of R
10, R
11, and R
12 has a number-average molecular weight of preferably 700 or greater, more preferably
900 or greater and preferably 3,500 or less, more preferably 2,500 or less, and particularly
preferably 1,500 or less. A polybutenyl group having a number-average molecular weight
of 700 or greater makes it possible to produce a lubricating oil composition with
excellent detergent and dispersion properties. Whereas, a polybutenyl group having
a number-average molecular weight of 3,500 or less makes it possible to produce a
lubricating oil composition with more excellent low-temperature flowability. With
the objective of excellent advantageous effects of suppressing sludge formation, the
lower limit of n is 2 and preferably 3, while the upper limit of n is 7 and preferably
6. The polybutenyl group can be obtained from polybutene (polyisobutene) produced
by polymerizing a mixture of 1-buten and isobutene or a highly purified isobutene
using a catalyst such as aluminum chloride or boron fluoride. The polybutene mixture
contains polybutenes having a vinylidene structure at the terminal ends in an amount
of generally 5 to 100 percent by mol. The polybutene (polyisobutene) may be those
of which a slight amount of the remaining fluorine and chlorine resulting from the
catalyst used in the process has been removed with a suitable treatment. Therefore,
the content of halogen atoms such as fluorine and chlorine is preferably 50 ppm by
mass or less, more preferably 10 ppm by mass or less, further more preferably 5 ppm
by mass or less, and particularly preferably 1 ppm or less.
[0039] No particular limitation is imposed on the method of producing the succinimide represented
by formula (2) or (3). For example, the succinimide may be produced by reacting a
polybutenyl succinimide produced by reacting polybutene obtained by chlorinating the
above polybutene, preferably one from which chorine and fluorine has been removed
with maleic anhydride at a temperature of 100 to 200 °C, with polyamine such as diethylene
triamine, triethylene tetramine, tetraethylene pentamine or pentaethylene hexamine.
In the case of producing the bissuccinimide, the polybutenyl succinimide in an amount
(molar ratio) of twice as much as polyamine may be reacted therewith, while in the
case of producing the monosuccinimide, the polybucenyl succinimide in the same amount
(molar ratio) may be reacted therewith.
[0040] The succinimide derivative may be a compound obtained by neutralizing or amidizing
the whole or part of the remaining amino groups and/or imide groups by allowing a
compound of formula (2) or (3) to react with an oxygen-containing organic compound
or a boron compound.
[0041] Specific examples of the oxygen-containing organic compound include monocarboxylic
acids having 1 to 30 carbon atoms, such as formic acid, acetic acid, glycolic acid,
propionic acid, lactic acid, butyric acid, valeric acid, caproic acid, enanthic acid,
caprylic acid, pelargonic acid, capric acid, undecylic acid, lauric acid, tridecanoic
acid, myristic acid, pentadecanoic acid, palmitic acid, margaric acid, stearic acid,
oleic acid, nonadecanoic acid, and eicosanoic acid; polycarboxylic acid having 2 to
30 carbon atoms, such as oxalic acid, phthalic acid, trimellitic acid, and pyromellitic
acid, anhydrides thereof, and ester compounds thereof; alkyleneoxides having 2 to
6 carbon atoms, and hydroxy(poly)oxyalkylene carbonates. By allowing such oxygen-containing
organic compounds to react as described above, the whole or part of the amino or imino
group in the compound of formula (2) or (3) assumedly has a structure as represented
by formula (4):

[0042] In formula (4), R
13 is hydrogen, an alkyl, alkenyl or alkoxy group having 1 to 24 carbon atoms, or a
hydroxy(poly)oxyalkylene group represented by -O-(R
14O)
mH wherein R
14 is an alkylene group having 1 to 4 carbon atoms, and m is an integer of from 1 to
5.
[0043] Examples of the boron compound include boric acid, borates, and boric acid esters.
Specific examples of boric acid include orthoboric acid, methaboric acid, and tetraboric
acid. Examples of borates include alkali metal salts, alkaline earth metal salts,
or ammonium salts, of boric acid. More specific examples include lithium borate such
as lithium methaborate, lithium tetraborate, lithium pentaborate, and lithium perborate;
sodium borate such as sodium methaborate, sodium diborate, sodium tetraborate, sodium
pentaborate, sodium hexaborate, and sodium octaborate; potassium borate such as potassium
methaborate, potassium tetraborate, potassium pentaborate, potassium hexaborate, and
potassium octaborate; calcium borate such as calcium methaborate, calcium diborate,
tricalcium tetraborate, pentacalcium tetraborate, and calcium hexaborate; magnesium
borate such as magnesium methaborate, magnesium diborate, trimagnesium tetraborate,
pentamagnesium tetraborate, and magnesium hexaborate; and ammonium borate such as
ammonium methaborate, ammonium tetraborate, ammonium pentaborate, and ammonium octaborate.
Examples of the boric acid esters include esters of boric acid and an aliphatic alcohol
having 1 to 6 carbon atoms and more specifically monomethyl borate, dimethyl borate,
trimethyl borate, monoethyl borate, diethyl borate, triethyl borate, monopropyl borate,
dipropyl borate, tripropyl borate, monobutyl borate, dibutyl borate, and tributyl
borate.
[0044] No particular limitation is imposed on the mass ratio of boron and nitrogen (B/N
ratio) in the succinimide reacted with a boron compound. However, the mass ratio is
preferably from 0.1 to 1.2, more preferably from 0,2 to 1.0, and particularly preferably
from 0.3 to 0.9 with the objective of enhancing the base number retaining properties
and high-temperature detergency.
[0045] In the present invention, one or more selected from the above-described succinimides
and derivatives thereof may be used as Component (B).
[0046] In the present invention, the lower limit content of Component (B) is 0.01 percent
by mass, preferably 0.05 percent by mass, and particularly preferably 0.08 percent
by mass in terms of nitrogen, based on the total mass of the composition. The upper
limit content of Component (3) is 0.3 percent by mass, preferably 0.2 percent by mass,
and particularly preferably 0.15 percent by mass in terms of nitrogen, based on the
total mass of the composition. Component (B) of less than 0.01 percent by mass would
fail to achieve the advantageous effect of the present invention, while Component
(B) of more than 0.3 percent by mass would deteriorate the low-temperature viscosity
characteristics and anti-emulsion properties of the resulting lubricating oil composition.
[0047] Component (C) of the lubricating oil composition of the present invention is an alkali
metal or alkaline earth metal detergent. Component (C) include alkali metal or alkaline
earth metal sulfonates, alkali metal or alkaline earth metal phenates, and alkali
metal or alkaline earth metal salicylates. One or more alkali metal or alkaline earth
metal detergents selected from the above compounds may be used, and particularly alkaline
earth metal detergents are preferably used in the present invention.
[0048] Preferred alkaline earth metal sulfonates are alkaline earth metal salts, such as
magnesium and/or calcium salts, preferably calcium salts, of alkyl aromatic sulfonic
acids obtained by sulfonating alkyl aromatic compounds having a molecular weight of
300 to 1,500 and preferably 400 to 700.
[0049] Specific examples of the alkyl aromatic sulfonic acids include petroleum sulfonic
acids and synthetic sulfonic acids.
[0050] Petroleum sulfonic acids may be those obtained by sulfonating alkyl aromatic compounds
contained in the lubricant fraction of a mineral oil or mahogany acid by-produced
upon production of white oil. The synthetic sulfonic acid may be those obtained by
sulfonating an alkyl benzene having a straight-chain or branched alkyl group, by-produced
from a plant for producing an alkyl benzene used as materials of detergents or obtained
by alkylating an oligomer of an olefin having 2 to 12 carbon atoms such as ethylene
and propylene to benzene or those obtained by sulfonating an alkylnaphthalene such
as dinonylnaphthalene. Although not restricted, sulfonating agents used for sulfonating
these alkyl aromatic compounds may be generally fuming sulfuric acids and sulfuric
acid anhydride.
[0052] In formulas (5) , (6), and (7), R
21, R
22, R
23, R
24, R
25, and R
26 may be the same or different from each other and are each independently a straight-chain
or branched alkyl group having 4 to 30, preferably 6 to 18 carbon atoms, M
1, M
2, and M
3 are each independently an alkaline earth metal, preferably calcium and magnesium,
and x is an integer of 1 or 2.
[0053] Specific examples of the alkyl group of R
21, R
22, R
23, R
24, R
25, and R
26 include butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl,
tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, heneicosyl,
docosyl, tricosyl, tetracosyl, pentacosyl, hexacosyl, heptacosyl, octacosyl, nonacosyl,
and triacontyl groups. These alkyl groups may be straight-chain or branched and may
be of primary, secondary, or tertiary.
[0054] Examples of the alkaline earth metal salicylates include alkaline earth metal salts,
preferably magnesium and calcium salts, of an alkyl salicylic acid. Specific examples
include compounds represented by formula (8)

[0055] In formula (8) , R
27 is a straight-chain or branched alkyl group having 4 to 30, preferably 6 to 18 carbon
atoms and M
4 is an alkaline earth metal, preferably calcium or magnesium.
[0056] Specific examples of the alkyl group of R
27 include butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl,
tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, heneicosyl,
docosyl, tricosyl, tetracosyl, pentacosyl, hexacosyl, heptacosyl, octacosyl, nonacosyl,
and triacontyl groups. These alkyl groups may be straight-chain or branched and may
be of primary, binary or tertiary.
[0057] The alkaline earth metal sulfonates, alkaline earth metal phenates, and alkaline
earth metal salicylates may be (1) neutral (normal salt) alkaline earth metal sulfonates,
neutral (normal salt) alkaline earth metal phenates, and neutral (normal salt) alkaline
earth metal salicylates obtained by reacting alkyl aromatic sulfonic acids, alkylphenols,
alkylphenolsuflides, Mannich reaction products of alkylphenol or alkyl salicylic acid
as mentioned above directly with an alkaline earth metal base of the oxide or hydroxide
of an alkaline earth metal such as magnesium and/or calcium or obtained by converting
alkyl aromatic sulfonic acids, alkylphenols, alkylphenolsuflides, Mannich reaction
products of alkylphenol or alkyl salicylic acid to an alkali metal salt such as sodium
salt and potassium salt, followed by substitution with an alkaline earth metal salt;
(2) basic alkaline earth metal sulfonates, basic alkaline earth metal phenates, and
basic alkaline earth metal salicylates obtained by heating the neutral alkaline earth
metal sulfonates, neutral alkaline earth metal phenates or neutral alkaline earth
metal salicylates with an excess amount of an alkaline earth metal salt or alkaline
earth metal base in the presence of water; and (3) overbased alkaline earth metal
sulfonates, overbased alkaline earth metal phenates and overbased alkaline earth metal
salicylates obtained by reacting the hydroxide of an alkaline earth metal with carbonic
acid gas or boric acid in the presence of the neutral alkaline earth metal sulfonates,
neutral alkaline earth metal phenates or neutral alkaline earth metal salicylates.
[0058] The above-described neutral alkaline earth metal salts, basic alkaline earth metal
salts, overbased alkaline earth metal salts, and mixtures thereof may be used in the
present invention. Although not restricted, the base number of these compounds is
generally 500 mgKOH/g or less, preferably from 60 mgKOH/g to 400 mgKOH/g. The term
"base number" used herein denotes a base number measured by the perchloric acid potentiometric
titration method in accordance with section 7 of JIS K2501 (1992) "Petroleum products
and lubricants-Determination of neutralization number".
[0059] Although alkaline earth metal detergents are usually commercially available in the
form of diluted with a light lubricating base oil, it is preferable to use metal detergents
of which metal content is within the range of 1.0 to 20 percent by mass and preferably
2.0 to 16 percent by mass.
[0060] No particular limitation is imposed on the metal ratio of Component (C). However,
it is preferable to use Component (C) whose metal ratio is generally 1 to 20, preferably
1 to 15.
[0061] In the present invention, Component (C) preferably contains the alkali metal or alkaline
earth metal salicylate detergent as an essential component. The metal ratio of the
detergent is preferably 3 or less, more preferably 2.6 or less, further more preferably
2 or less, and particularly preferably 1.5 or less. The alkali metal or alkaline earth
metal salicylate detergent may be used singlely or in the form of a mixture of those
of different metal ratios. For example, an alkali metal or alkaline earth metal salicylate
with a metal ratio of 2 or less, preferably 1.5 or less, and particularly preferably
1.2 or less may be used alone as an essential component. Alternatively, an alkali
metal or alkaline earth metal salicylate with a metal ratio of 1.5 or less, preferably
1.2 or less may be used in combination with one with a metal ratio in excess of 1.5,
particularly 2.6, and the metal ratio of the mixture is adjusted to 1.3 or more and
preferably 2.3 or less, more preferably 2 or less, and particularly preferably 1,5
or less. Component (C) can enhance base number retaining properties, high-temperature
detergency, and low friction characteristics by adjusting the metal ratio to be within
the range of 1.3 to 2.3, even though the content of Component (C) is maintained the
same.
[0062] Component (C) is preferably a combination of an alkali metal or alkaline earth metal
salicylate with a metal ratio of 1.5 or less, preferably 1.2 or less and an alkali
metal or alkaline earth metal sulfonate. No particular limitation is imposed on the
metal ratio of the alkali metal or alkaline earth metal sulfonate. However, the metal
ratio is generally from 1 to 20, preferably from 1 to 15, and particularly preferably
from 5 to 12. Component (C) thus prepared can further enhance advantageous effect
to improve base number retaining properties, high-temperature detergency, and low
friction characteristics.
[0063] The term "metal ratio" used herein is represented by "valence of metal element x
metal element content (mol) / soap group (group such as alkylsalicylic acid group)
content (mol)" and denotes the alkali metal or alkaline earth metal content against
the content of the alkylsalicylic acid and alkylsulfonic acid groups in an alkali
metal or alkaline earth metal detergent.
[0064] The lower limit content of Component (C) is 0.05 percent by mass, preferably 0.1
percent by mass, more preferably 0.15 percent by mass, and particularly preferably
0.2 percent by mass in terms of alkali metal or alkaline earth metal, based on the
total mass of the lubricating oil composition of the present invention. The upper
limit content of Component (C) is 1 percent by mass, preferably 0.5 percent by mass,
and more preferably 0.4 percent by mass in terms of alkali metal or alkaline earth
metal, based on the total mass of the lubricating oil composition of the present invention.
Component (C) of less than 0.05 percent by mass would fail to exhibit excellent base
number retaining properties and high-temperature detergency, while Component (C) of
more than 1 percent by mass would fail to attain effects as expected.
[0065] Component (D) of the lubricating oil composition of the present invention is a phenol-
and/or amine-based anti-oxidant.
[0066] Examples of the phenol-based anti-oxidant include 4,4'-methylenebis(2,6-di-tert-butylphenol),
4,4'-bis(2,6-di-tert-butylphenol), 4,4'-bis(2-methyl-6-tert-butylphenol), 2,2'-methylenebis(4-ethyl-6-tert-butylphenol),
2,2'-methylenebis(4-methyl-6-tert-butylphenol), 4,4'-butylidenebis(3-methyl-6-tert-butylphenol),
4,4'-isopropylidenebis(2,6-di-tert-butylphenol), 2,2'-methylenebis(4-methyl-6-nonylphenol),
2,2'-isobutylidenebis(4,6-dimethylphenol), 2,2'-methylenebis(4-methyl-6-cyclohexylphenol),
2,6-di-tert-butyl-4-methylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2,4-dimethyl-6-tert-butylphenol,
2,6-di-tert-α -dimethylamino-p-cresol, 2,6-di-tert-butyl-4 (N,N'-dimethylaminomethylphenol),
4,4'-thiobis(2-methyl-6-tert-butylphenol), 4,4'-thiobis(3-methyl-6-tert-butylphenol),
2,2'-thiobis(4-methyl-6-tert-butylphenol), bis(3-methyl-4-hydroxy-5-tert-butylbenzyl)sulfide,
bis(3,5-di-tert--butyl-4-hydroxybenzyl)sulfide, 2,2'-thio-diethylenebis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate],
tridecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate, pentaerythrityl-tetraquis
[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate], octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)
propionate, octyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate, and octyl-3- (3-methyl-5-tert-butyl-4-hydroxyphenyl)
propionate. Two or more of these phenol-based anti-oxidants may be used in combination.
[0067] Specific examples of the amine-based anti-oxidant include phenyl-α-naphtylamine,
alkylphenyl-α -naphtylamine, and dialkyldiphenylamine. Two or more of these amine-based
anti-oxidants may be used in combination. The above alkyl groups are those having
1 to 16 carbon atoms.
[0068] The above-described phenol-based and amine-based anti-oxidants may be used singlely
but preferably used in combination because the advantageous effects can be further
enhanced.
[0069] The lower limit content of Component (D) is 0.01 percent by mass, preferably 0.1
percent by mass, more preferably 0.5 percent by mass, and particularly preferably
1.0 percent by mass, based on the total mass of the lubricating oil composition of
the present invention with the objective of further enhancing the base number retaining
properties and high-temperature detergency. The upper limit content of Component (D)
is 3.0 percent by mass and preferably 2.5 percent by mass, based on the total mass
of the lubricating oil composition of the present invention. Component (D) of more
than 3.0 percent by mass would fail to attain sufficient anti-oxidant properties as
balanced with the content.
[0070] The lubricating oil composition of the present invention may contain an anti-wear
agent other than Component (A).
[0071] Examples of an anti-wear agent other than Component (A) include phosphorus- and/or
sulfur-containing anti-wear agents such as thiophosphates and metal salts of phosphates,
represented by formula (9) and thiophosphates, phosphates, and metal salts and amine
salts thereof, represented by formula (10) and further include those such as phosphites,
thiophosphites, and metal salts and amine salts thereof, thiotriphosphtes, zinc dialkyldithiophosphates,
zinc dialkyldithiocarbamates, molybdenum dialkyldithiophosphates, molybdenum dialkyldithiocarbamates,
disulfides, olefin sulfides, and sulfurized fats and oils:

[0072] In formulas (9) and (10) , R
30, R
31, R
32, R
33, R
34, and R
35 are each independently hydrogen or a hydrocarbon group having 1 to 30 carbon atoms.
Examples and preferred examples of the hydrocarbon group having 1 to 30 carbon atoms
include the same as those exemplified with respect to R
1 in formula (1) representing Compound (A) described above.
[0073] X
1, X
2, X
3, X
4, X
5, and X
6 are each independently oxygen or sulfur, at least one of them is oxygen, and preferably
two or more of them are oxygen, and particularly preferably all of them are oxygen.
Due to the presence of at least one oxygen, the resulting composition can be decreased
in sulfur content and in the amount of sulfuric acid produced when being oxidized
or thermally decomposed and thus can be significantly suppressed in the exhaust of
the base number.
[0074] Y is a metal atom and specifically zinc, copper, iron, lead, nickel, silver, and
manganese. With the objective of enhanced anti-wear properties, Y is preferably zinc.
[0075] U is hydrogen (proton), a monovalent metal ion, or an ammonium ion. k indicates the
number of ion of U and is an integer of from 1 to 20, preferably from 1 to 10, and
more preferably from 1 to 8.
[0076] The monovalent metal ion of U is a metal atom which can form a salt and thus may
be an alkali metal, such as lithium, sodium, potassium and cesium. The ammonium ion
may be those providing ammonium ion such as nitrogen-containing compounds which can
form an amine salt.
[0077] Examples of nitrogen-containing compounds include ammonia, monoamines, diamines,
and polyamines . More specific examples include alkylamines having a straight-chain
or branched alkyl group having 1 to 30 carbon atoms, such as methylamine, ethylamine,
propylamine, butylamine, pentylamine, hexylamine, heptylamine, octylamine, nonylamine,
decylamine, undecylamine, dodecylamine, tridecylamine, tetradecylamine, pentadecylamine,
hexadecylamine, heptadecylamine, octadecylamine, dimethylamine, diethylamine, dipropylamine,
dibutylamine, dipentylamine, dihexylamine, diheptylamine, dioctylamine, dinonylamine,
didecylamine, diundecylamine, didodecylamine, ditridecylamine, ditetradecylamine,
dipentadecylamine, dihexadecylamine, diheptadecylamine, dioctadecylamine, methylethylamine,
methylpropylamine, methylbutylamine, ethylpropylamine, ethylbutylamine, and propylbutylamine;
alkenylamines having a straight-chain or branched alkenyl group having 2 to 30 carbon
atoms, such as ethenylamine, propenylamine, butenylamine, octenylamine and oleylamine;
alkanolamines having a straight-chain or branched alkanol group having 1 to 30 carbon
atoms, such as methanolamine, ethanolamine, propanolamine, butanolamine, pentanolamine,
hexanolamine, heptanolamine, octanolamine, nonanolamine, methanolethanolamine, methanolpropanolamine,
methanolbutanolamine, ethanolpropanolamine, ethanolbutanolamine, and propanolbutanolamine;
alkylenediamines having an alkylene group having 1 to 30 carbon atoms, such as methylenediamine,
ethylenediamine, propylenediamine, and butylenediamine; polyamines such as diethylenetrimaine,
triethylenetetramine, tetraethylenepentamine, and pentaethylenehexamine; heterocyclic
compounds such as undecyldiethylamine, undecyldiethanolamine, dodecyldipropanolamine,
oleyldiethanolamine, oleylpropylenediamine, and stearyltetraethylenepentamine, having
an alkyl or alkenyl group having 8 to 20 carbon atoms bonded to the above-exemplified
monoamines, diamines and polyamines and N-hydroxyethyloleylimidazoline; alkylene oxide
adducts thereof; and mixtures thereof.
[0078] In the case of using an anti-wear agent containing sulfur selected from the above
anti-wear agents other than Component (A) , no particular limitation is imposed on
the content of the anti-wear agents. However, the content is preferably 0.1 percent
by mass or less and more preferably 0.09 percent by mass or less in terms of sulfur,
based on the total mass of the lubricating oil composition of the present invention.
However, it is particularly preferable not to use the sulfur-containing anti-wear
agent. A lubricating oil composition with significantly excellent base number retaining
properties and high-temperature detergency can be obtained by decreasing the amount
of the sulfur-containing anti-wear agent to 0.1 percent by mass or less.
[0079] In the case of blending a sulfur-free phosphorus-containing anti-wear agent selected
from the above-described anti-wear agents other than Component (A), the content is
from 0.01 to 0.2 percent by mass in terms of phosphorus, based on the total mass of
the lubricating oil 1 composition of the present invention. Even in such a case, the
total content of the anti-wear agent and Component (A) does not exceed preferably
0.2 percent by mass and particularly preferably 0.15 percent by mass in terms of phosphorus,
based on the total mass of the composition because there is a risk that exhaust gas
purifying catalysts are adversely affected.
[0080] Although the lubricating oil composition for internal combustion engines of the present
invention is excellent in anti-wear properties, base number retaining properties,
and high-temperature detergency, various additives may be optionally added in order
to further improve these properties. Examples of such additives include viscosity
index improvers, ashless dispersants other than Component (B), metal detergents other
than Component (C), anti-oxidants other than Component (D), friction modifiers, corrosion
inhibitors, rust preventives, anti-emulsifiers, metal deactivators, anti-foamers,
and dyes.
[0081] Examples of viscosity index improvers include non-dispersion type viscosity index
improvers such as copolymers of one or more monomers selected from venous methacrylates
or hydrides thereof; dispersion type viscosity index improvers such as copolymers
of various methacrylates further containing nitrogen compounds; non-dispersion- or
dispersion-type ethylene-α-olefin copolymers of which the α-olefin may be propylene,
1-butene, or 1-pentene, or the hydrides thereof; polyisobutylenes or the hydrides
thereof; styrene-diene hydrogenated copolymers; styrene-maleic anhydride ester copolymers;
and polyalkylstyrenes.
[0082] It is necessary to select the molecular weight of these viscosity index improvers
considering the shear stability thereof. Specifically, the number-average molecular
weight of non-dispersion or dispersion type polymethacrylates is from 5,000 to 1,000,000
and preferably from 10,000 to 350,000. The number-average molecular weight of polyisobutylenes
or hydrides whereof is from 800 to 5,000 and preferably from 1,000 to 4,000. The number-average
molecular weight of ethylene-α-olefin copolymers and hydrides thereof is from 800
to 500,000 and preferably from 3,000 to 200,000.
[0083] Among these viscosity index improvers, the use of ethylene-α-olefin copolymers or
hydrides thereof is contributive to production of a lubricating oil composition which
is excellent particularly in shear stability. One or more compounds selected from
the above-described viscosity index improvers may be blended in an arbitrary amount.
The content of the viscosity index improvers is generally within the range of 0.1
to 20.0 percent by mass, based on the total mass of the lubricating oil composition.
[0084] Examples of ashless dispersants other than Component (B) include benzylamines having
in the molecules at least one alkyl or alkenyl group having 40 to 400 carbon atoms
and derivatives thereof; and polyamines having in the molecules at least one alkyl
or alkenyl group having 40 to 400 carbon atoms and derivatives thereof.
[0085] Examples of friction modifiers include aliphatic amines, fatty acids, fatty acid
esters, and aliphatic alcohols, having an alkyl or alkenyl group having 6 to 30 carbon
atoms.
[0086] Examples of corrosion inhibitors include benzotriazole-, tolyltriazole-, thiazole-,
thiadiazole-, and imidazole-based compounds.
[0087] Examples of rust-preventives include petroleum sulfonates, alkylbenzene sulfonates,
dinonylnaphthalenesulfonates, alkenyl succinic acid esters, and polyhydric alcohol
esters.
[0088] Examples of anti-emulsifiers include polyalkylene glycol-based non-ionic surfactants
such as polyoxyethylenealkyl ether, polyoxyethylenealkylphenyl ether, and polyoxyethylenealkylnaphthyl
ether.
[0089] Examples of metal deactivators include imidazolines, pyrimidine derivatives, alkylhiadiazoles,
mercaptobenzothiazoles, benzotriazoles and derivatives thereof, 1,3,4-thiadiazolepolysulfide,
1,3,4-thiadiazolyl-2,5-bisdialkyldithiocarbamte, 2-(alkyldithio)benzoimidazole, and
β -(o-carbaxybenzylthio)propionitrile.
[0090] Examples of anti-foamers include silicone, fluorosilicone, and fluoroalkyl ether.
[0091] When these additives are added to the lubricating oil composition of the present
invention, the content of each of the ashless dispersant other than Component (B),
metal detergent other than Component (C), anti-oxidant other than Component (D), friction
modifier, corrosion inhibitor, rust inhibitor, and anti-emulsifier is 0.01 to 5 percent
by mass based on the total mass of the composition. The content of the metal deactivator
is 0.005 to 1 percent by mass, while the content of the anti-foamer is 0.0005 to 1
percent by mass.
[0092] The lubricating oil composition of the present invention is preferably limited in
the content of additive containing sulfur as well as the content of the above-described
sulfur-containing anti-wear agent. The content of the sulfur-containing additive including
the sulfur-containing anti-wear agent is preferably 0.1 percent by mass or less and
more preferably 0.09 percent by mass or less based on the total mass of the composition.
Particularly preferably the lubricating oil composition contains no sulfur-containing
additives including the sulfur-containing anti-wear agent. Although commercially available
additives generally contain a solvent used when they are synthesized or a diluting
oil such as a solvent-refined mineral oil used to improving the handleability of the
additives, the term "sulfur-containing additives" used herein does not refer to sulfur
compounds derived from such a solvent or diluting oil.
[0093] Even though the composition of the present invention contains sulfur originating
from the solvent or diluting oil, the total sulfur content of the composition is 0.2
percent by mass or less, preferably 0.15 percent by mass or less, and particularly
preferably 0.1 percent by mass or less. As a result, a composition which is excellent
in anti-wear properties, base number retaining properties, and high-temperature detergency
and capable of maintaining the performance of exhaust gas purifying catalysts can
be obtained. In the present invention, a composition containing sulfur in an amount
of 10 ppm by mass or less or containing substantially no sulfur can be obtained using
a high-degree hydrocracked base oil. whose content of sulfur originating from a solvent
or diluting oil is 10 ppm by mass or less or a base oil produced by isomerizig GTL
Wax (Gas To Liquid Wax) or a synthetic oil, containing substantially no sulfur.
[Applicability in the Industry]
[0094] Even though the lubricating oil composition for internal combustion engines, of the
present invention is decreased in the amount of a sulfur-containing agent such as
ZDTP having both anti-wear and anti-oxidation properties or contains no such an agent
at all, the composition is extremely improved in anti-oxidation properties and in
base number retaining properties, i.e., long-drain properties, and also excellent
in high-temperature detergency and low friction characteristics, but free from the
decrease of anti-wear properties.
[0095] Furthermore, since the total sulfur content of the lubricating oil composition of
the present invention can be held down and prevented from raising more than 0.2 percent
by mass, the composition can suppress exhaust gas purifying catalysts from poisoning
by sulfur and be used suitably for engines equipped with an exhaust-gas after-treatment
device such as an exhaust gas purifying catalyst.
[0096] Moreover, the lubricating oil composition of the present invention can also be used
suitably as lubricating oils required to have anti-wear properties, base number retaining
properties, and high-temperature detergency, such as lubricating oils for driving
means such as automatic or manual transmissions; those for wet brakes; hydraulic oils;
turbine oils; gear oils; and bearing oils.
[Best Mode for Carrying out the Invention]
[0097] Hereinafter, the present invention will be described in more details by way of the
following examples and comparative examples, which should not be construed as limiting
the scope of the invention.
(Examples 1 to 4 and Comparative Examples 1 and 2)
[0098] Lubricating oil compositions for internal combustion engines, each having the formulation
and properties shown in Table 1 were prepared. The compositions containing 0.05 percent
by mass of sulfur are those containing sulfur originating from the diluting oils contained
in the additives.
[0099] The compositions of Examples 1 to 4 and Comparative Examples 1 and 2 were evaluated
by the following performance characteristics evaluating tests.
(1) Changes in base number with time by ISOT
[0100] Each of the compositions was forced to deteriorate at a temperature of 165.5 °C in
accordance with "Lubricating Oils for Internal Combustion Engine-Determination of
Oxidation Stability Test" (Indiana Stirring Oxidation Test (ISOT), JIS K 2514) and
measured for change in base number (hydrochloric acid method) with time. The results
are shown in Table 1. A higher base number remaining rate indicates that the composition
was enhanced in base number retaining properties and thus found to be a long drain
oil which was able to be used for a long period of time.
[0101] As shown in Table 1, the compositions of the present invention (Examples 1 to 4)
were significantly higher in base number retaining properties than the compositions
(Comparative Examples 1 and 2) containing ZDTP (sulfur-containing anti-wear agent)
in such a general amount that they are used as lubricating oils for internal combustion
engines, i.e., 0.16 percent by mass in terms of sulfur and 0.08 percent by mass in
terms of phosphorus. The triphenylphosphate-containing compositions (Example 4) and
particularly the tributylphosphate-containing composition (Example 3) were significantly
higher in base number retaining properties that the trioctylphosphate-containing composition
(Example 1).
(2) Changes in base number with time measured by a NOx absorbing test
[0102] Each of the sample oils was forced to deteriorate by blowing thereto a NOx gas under
the conditions (150 °C, NOx : 1185 ppm) in compliance with those described in "Japanese
Society of Tribologists Conference Preliminary Reports 1992, 10, 465" and measured
for change in base number (hydrochloric acid method) with time. The results are shown
in Table 1. A smaller reduction in base number indicates that the composition is enhanced
in base number retaining properties even in the presence of NOx as used in an internal
combustion engine and is a long drain oil which can be used for a long period time.
[0103] As shown in Table 1, the compositions of the present invention (Examples 1 to 4)
were found to exhibit excellent base number retaining properties and long drain properties
under such an atmosphere that lubricating oils for internal combustion engines are
exposed to NOx, similarly to the results in the above-described ISOT.
(3) Anti-wear properties evaluated by FALEX test
[0104] The seizuring load of each of sample pieces was measured by FALEX test in accordance
with ASTM D3233 (A method, 290 rpm, room temperature) . The results are shown in Table
1. The larger the seizuring load, the composition exhibits more excellent anti.-wear
properties.
[0105] As shown in Table 1, the anti-wear properties of the compositions of the present
invention were equal to or higher than those of Comparative Examples 1 and 2.
(4) High-temperature detergency evaluated by a hot tube test
[0106] A hot tube test was conducted in accordance with JPI-5S-5599. The evaluation was
made by grading the compositions as 10 points when they were colorless and transparent
(no fouling) and those as 0 point when they were black and opaque. Between 10 and
0 point, evaluation was done using reference tubes which were made per grade beforehand.
At 290 °C, 6 points or higher indicate that the oil composition has an excellent detergency
for an ordinary gasoline or diesel engine. However, a lubricating oil composition
for a gas engine preferably exhibits excellent detergency also at 300°C or higher
in this test.
[0107] It is confirmed from Table 1 that the compositions of the present invention exhibited
extremely excellent high-temperature detergency even at a temperature of 300 °C or
higher. Particularly, the composition containing trioctylphosphate which is conceivably
lower in evaporation than tributylphosphate exhibited extremely excellent high-temperature
detergency.
(Examples 5 to 9 and Comparative Example 3)
[0108] Lubricating oil compositions (Examples 5 to 9 and Comparative Example 3) with the
formulations and properties shown in Table 2 were prepared and evaluated by the following
test. The results are shown in Table 2. The composition of Example 9 is the same as
the one of Example 1 in Table 1, while the composition of Comparative Example 3 is
the same as the one of Comparative Example 1 in Table 1.
(5) Low-friction characteristics evaluated by an LFW-1 boundary friction test
[0109] An LFM-1 boundary friction test was conducted at a load of 100 lbs, a temperature
of 100°C, and various speeds using an LFW-1 boundary friction tester.
[0110] As apparent from the results shown in Table 2, the composition of Example 9 (composition
of Example 1 in Table 1) is also excellent in low friction characteristics, compared
with the composition of Comparative Example 3 (composition of Comparative Example
1 in Table 1. The compositions containing a low metal ratio alkaline earth metal salicylate
essentially as Component (C) (Examples 5 to 8) were found to exhibit extremely superior
low friction characteristics. These compositions exhibited base number retaining properties,
anti-wear properties, and high temperature detergency equally to or better than the
composition of Example 9. Component (C) of the composition of Example 6 was a mixture
of calcium salicylate whose metal ratio is 1.0 and calcium salicylate whose metal
ratio is 2.7, and the total metal ratio of Component (C) is 1.46. However, the composition
of Example 6 contained less amount of Component (C) of Example 5 but was recognized
to be decreased in friction coefficient particularly in the high velocity region synergistically,
compared with the average between Examples 5 and 9 . In the case of using tributylphosphate
or triphenylphosphate instead of trioctylphosphate as Component (A), the composition
containing tributylphosphate or triphenylphosphate was superior in low friction characteristics
to Comparative Example 3 but the composition containing trioctylphosphate exhibited
the most excellent low friction characteristics.
[0111] The "mass %" in the tables is based on the total mass of the composition.
