[0001] This invention relates to improved lubricating oils having excellent characteristics
in anti-wear, detergency, oxidation stability and viscosity-temperature correlation.
Especially, this invention relates to an engine oil that is hardly deteriorated on
contact with nitrogen oxide gas (NOx) and that can work stably for a long time.
BACKGROUND OF THE INVENTION
[0002] Automobile spark ignition and diesel engines have valve train systems, including
valves, cams and rocker arms, which present special lubrication concerns. It is extremely
important that the engine oil protects these parts from wear. Further, it is important
for engine oils to suppress the production of deposits in the engines. Such deposits
are produced from non-combustibles and incomplete combustibles of hydrocarbon fuels
(e.g., gasoline, diesel fuel oil) and by the deterioration of the engine oil employed.
[0003] Engine oils use a mineral oil or a synthetic oil as a base oil. However, simple base
oils alone do not provide the necessary properties to provide the necessary wear protection,
deposit control, etc., required to protect internal combustion engines. Thus, base
oils are formulated with various additives, for imparting auxiliary functions, such
as ashless dispersants, metallic detergents (i.e., metal-containing detergents), antiwear
agents, antioxidants (i.e., oxidation inhibitors), viscosity index improvers and the
like to give a compounded oil (i.e., a lubricating oil composition).
[0004] Meanwhile, combustion gas produced in a gasoline engine or a diesel engine is mostly
exhausted from the exhaust pipe as exhaust gas, but a portion of the combustion gas
leaks through a gap between piston and cylinder to blow into the crankcase as blow-by
gas. Since the blow-by gas contains nitrogen oxide gas (NO
X) of high concentration, it oxidizes and deteriorates an engine oil (crank case oil)
charged in the crank case. Recently, since lightweight motor cars are required in
view of saving energy (improving fuel-efficiency), the crank cases of the engines
are apt to be made small. Therefore, the amount of the engine oil charged in such
a small crank case is lowered and the relative amount of nitrogen oxide introduced
into the crank case as blow-by gas per the amount of the charged engine oil is increased.
Consequently, the deterioration of engine oil is apt to be promoted. In addition to
the above-described reason, since recent engines are often used to satisfy severe
demands (high speed and/or high power), the concentration of nitrogen oxide in blow-by
gas is further increasing.
[0005] As is described above, factors in the deterioration of engine oils are more and more
increasing. Once an engine oil is deteriorated, its acid value is increased and sludge
is deposited in the crank case. Therefore, engine oils are desired to be protected
from the deterioration as far as possible. Hitherto, in order to inhibit the oxidation
and the deposition of sludge, additives such as oxidation inhibitors (e.g., zinc dithiophosphate,
oxidation inhibitors of phenol type) and detergent-dispersants (e.g., ashless dispersants,
metal-containing detergents) have been added to engine oils. However, since recent
engines are apt to be used under severe conditions as is described above, the known
additives cannot satisfactorily prevent engine oils from deteriorating. Therefore,
it is desired to take measures to meet this problem.
[0006] The use of phenol sulfides in lubricating oils is well known in the art.
[0007] U.S. Patent No. 3,236,770 discloses a lubricating oil having a dialkylthiocarbonate,
and either a metal dialkyl dithiophosphate; a basic alkaline earth metal sulfonate;
or a basic alkaline earth metal alkyl phenol sulfide.
[0008] U.S. Patent No. 3,240,705 discloses a 2,2'-trithiobis-(4-halo-6-alkylphenol).
[0009] U.S. Patent No. 4,302,683 discloses an organo-molybdenum complex prepared by reacting
a hydrocarbyl substituted thio-bis-phenol with a molybdenum source.
[0010] U.S. Patent No. 4,764,294 discloses an engine oil having a base oil, a metal phosphate,
a metal carbamate, and a para alkyl hydroxy-aryl sulfide.
[0011] The use of dithiocarbamates in lubricating oils is well known in the art.
[0012] U.S. Patent No. 3,876,550 discloses lubricating compositions containing an alkylene
bis(dithiocarbamate), as an antioxidant, and a substituted succinic acid as a rust
inhibitor. The alkylene dithiocarbamate is represented in the patent by the formula
R
1R
2N-C(S)-S-alkylene-S-C(S)-NR
3R
4. Example 5 of the patent describes a crankcase lubricant containing a viscosity improver,
an ashless dispersant and methylene bis(dibutyldithiocarbamate). The patent further
teaches that the composition may also contain various other additives, for example,
detergents, dispersants, viscosity improvers, extreme pressure agents, antiwear additives,
etc., as well as other oxidation inhibitors and corrosion inhibitors and cites an
extensive list of extreme pressure agents, corrosion inhibitors and antioxidants,
including zinc salts of phosphorodithoic acid.
[0013] The use of methylene bis(dibutyldithiocarbamate) as an oxidation inhibitor in lubricating
oils, in combination with other ingredients, is also disclosed in U.S. Patent Nos.
4,125,479 and 4,880,551.
[0014] U.S. Patent No. 4,879,054 is directed to cold temperature greases and teaches using
dithiocarbamates such as Vanlube 7723, i.e., 4,4'-methylene bis(dithiocarbamate),
in such greases to provide extreme pressure antiwear properties. Examples 13-18 describe
using Vanlube 7723 and triarylphosphate as replacements for lead naphthenate and zinc
dithiophosphate.
[0015] The use of dithiocarbamates as extreme pressure antiwear additives is also taught
by U.S. Patent No. 4,859,352, and U.S. Patent No. 4,648,985 teaches that the combination
of dithiocarbamates with zinc dithiophosphate and copper salts of carboxylic acid
provide lubricants with extreme pressure properties.
[0016] U.S. Patent No. 4,383,931 discloses using lubricating oils containing an oil-soluble
molybdenyl bis-β-di- ketonate in combination with zinc dithiophosphate. Methylene
bis(dihydrocarbyldithiocarbamates) are used as ashless antioxidants and extreme pressure
agents.
[0017] U.S. Patent No. 4,501,678 discloses using lubricating oils containing an alkyl thiocarbamoyl
compound and either a molybdenum thiocarbamoyl compound or a molybdenum organophosphorodithioate.
[0018] U.S. Patent No. 4,609,480 discloses using lubricating oils containing an alkyl thiocarbamoyl
compound and a 1,3,4-thiadiazole compound. The oils can also contain, among other
things, sulfurized oxymolydenum orga- nophosphorodithioates.
SUMMARY OF THE INVENTION
[0019] The present invention provides a low-phosphorous lubricating oil composition that
is hardly deteriorated on contact with nitrogen oxide gas (NO
X) and which can work stably for a long time. That composition has a major amount of
a base oil of lubricating viscosity, from 0.5 to 20 wt.% of metal-containing detergent,
from 0.1 to 3 wt.% of zinc dithiophosphate, from 0.5 to 15 wt.% of ashless dispersant,
and from 0.05 to 5 wt.% of a sulfur-containing phenol derivative.
[0020] The sulfur-containing phenol derivative is selected from the group consisting of:

and

wherein R
1, R
2, R
3, and R
8 are the same or different and each represents an alkyl group of 1 to 18 carbon atoms;
R
4, R
5, R
6, and R
7 are the same or different and each represents an alkylene group of 1 to 3 carbon
atoms; and R' represents an alkyl group of 1 to 4 carbon atoms.
[0021] Preferably, the sulfur-containing phenol derivative comprises 0.1 to 3 wt.% of the
composition. The alkyl groups of the sulfur-containing phenol derivative should have
1-14 carbon atoms. Examples of preferred sulfur-containing phenol derivatives are
2,4-bis{(octylthio)methyl}-o-cresol, 2,2-thio-diethylenebis{3-(3,5-di-t-butyl-4-hydroxyphenyl)
propionate}, or tridecyl 2-(3,5-di-t-butyl-4-hydroxybenzylthio)acetate.
[0022] Preferably, the low-phosphorous lubricating oil composition also has from 0.05 to
8 wt.% of an alkylthiocarbamoyl compound represented by the formula:

wherein R
9, R
10, R11 and R
12 are the same or different and each represents an alkyl group of 1-18 carbon atoms,
and (X) represents S, S-S, S-CH
2-S, S-CH
2-CH
2-S, S-CH
2-CH
2-CH
2-S or S-CH
2-CH(CH
3)-S. Preferably, R
9, R
10, R
11 and R
12 are independently selected from alkyl groups having 1 to 6 carbon atoms. More preferably,
the dithiocarbamate compound is methylene bis(dibutyldithiocarbamate).
[0023] Preferably, the zinc dithiophosphate is a secondary alkyl type.
[0024] This invention can further involve an additive concentrate having 100 weight parts
of a metal-containing detergent, from 10 to 700 weight parts of an ashless dispersant,
and from 2 to 200 weight parts of the sulfur-containing phenol derivative described
above.
[0025] It is an object of the present invention to provide an engine oil composition that
is hardly deteriorated on contact with nitrogen oxide gas (NO
X), and particularly to provide an engine oil composition that can work stably even
if exposed to nitrogen oxide gas of high concentration for a long time.
DETAILED DESCRIPTION OF THE INVENTION
[0026] In its broadest aspect, the present invention is an engine oil composition comprising
a base oil, an ashless dispersant, a metal-containing detergent, zinc dithiophosphate
and a sulfur- containing phenol derivative.
[0027] Representative examples of the sulfur-containing phenol derivative employed for the
invention are the compounds represented by the following formulae (1), (2) and (3):

and

wherein R
1, R
2, R
3 and R
8 are the same or different and each represents an alkyl group of 1-18 carbon atoms;
R
4, R
5, R
6 and R
7 are the same or different and each represents an alkylene group of 1-3 carbon atoms;
and R' represents an alkyl group of 1 to 4 carbon atoms.
[0028] The sulfur-containing phenol derivative of the formulae (I), (II) or (III) is dissolved
or dispersed in a base oil together with various additives, such as metal-containing
detergents, ashless dispersants, zinc dithiophosphate, viscosity index improvers and
the like, in the same manner as known engine oil compositions (i.e., engine oils).
[0029] A variety of metal-containing detergents, ashless dispersants, zinc dithiophosphates,
viscosity index improvers and base oils are known. These known materials or their
analogous compounds can be employed for the preparation of the engine oil of the invention.
Representative examples of these materials are described below.
BASE OIL
[0030] The base oil may be a mineral oil or synthetic oil or a blend of mineral oils and/or
synthetic oils blended to give a base oil of the desired internal combustion engine
oil viscosity. Typically, individually the oils used as its base oil will have a viscosity
range of about from 10 to 120 cST at 40°C and will be selected or blended depending
on the desired end use and the additives in the finished oil to give the desired grade
of engine oil.
METAL-CONTAINING DETERGENT
[0031] The metal-containing detergent may be a metal phenate or a metal sulfonate. The metal
phenate is an alkaline earth metal salt of sulfide of alkylphenol having an alkyl
group of about 8-30 carbon atoms. Generally employed alkaline earth metals are calcium,
magnesium and barium. The metal sulfonate is an alkaline earth metal salt of a sulfonated
aromatic compound or a sulfonated mineral oil derived from lubricating oil having
a molecular weight of about 400-600. Generally employed alkaline earth metals are
also calcium, magnesium and barium. The metal phenate and metal sulfonate can be used
singly or in combination. Also employed are other metal-containing detergents such
as salicylate, phosphonate and naphthenate of alkaline earth metals. These detergents
can be employed single or in combination. The aforementioned phenate and sulfonate
can be employed in combination with these other metal-containing detergents. The metal-containing
detergents may be of a neutral type or of an over-based type having an alkalinity
value of 150-300 or more.
[0032] The metal-containing detergent is generally incorporated into an engine oil in an
amount of 0.5-20 wt.% per total amount of the engine oil.
ASHLESS DISPERSANT
[0033] Examples of the ashless dispersant used for the invention include succinimides, succinic
esters, and benzylamine, each of which has an alkyl or alkenyl group of a molecular
weight of about 700-3,000. In addition to these compounds, their derivatives (e.g.,
borated derivatives) are also employable. The ashless dispersant is generally incorporated
into an engine oil in an amount of 0.5-15 wt.% per total amount of the engine oil.
ZINC DITHIOPHOSPHATE
[0034] The zinc dithiophosphate, used as an anti-wear agent or an oxidation inhibitor, generally
is zinc dihydrocarbyl-dithiophosphate having an alkyl group of 3-18 carbon atoms or
an alkylaryl group having an alkyl group of 3-18 carbon atoms. This agent is generally
incorporated into an engine oil in an amount of 0.1-3 wt.% per total amount of the
engine oil.
VISCOSITY INDEX IMPROVER
[0035] Examples of the viscosity index improvers are poly-(alkyl methacrylate), ethylene-propylene
copolymer, styrene-butadiene copolymer, and polyisoprene. Viscosity index improvers
of dispersant type (having increased dispersancy) or multi-function type are also
employed. These viscosity index improvers can be used singly or in combination. The
amount of viscosity index improver to be incorporated into an engine oil varies with
desired viscosity of the compounded engine oil, and generally in the range of 0.5-20
wt.% per total amount of the engine oil.
[0036] The engine oil of the invention may contain various additional additives other than
those described above, if desired. Examples of such additional additives include known
extreme pressure agents, corrosion inhibitors, rust inhibitors, friction modifiers,
anti-foaming agents and pour point depressants. In addition to these additives, other
oxidation inhibitors (e.g., hindered phenol), anti-wear agents and multi-functional
additives (e.g., organic molybdenum compounds such as molybdenum dithiophosphate)
may be employed in combination.
SULFUR-CONTAINING PHENOL DERIVATIVE
[0037] Details of the sulfur-containing phenol derivative characterizing the present invention
are described below.
[0038] As is described above, the sulfur-containing phenol derivative preferably used for
the invention is a compound represented by one of the following formulae (I), (11),
and (III):

and

wherein R
1, R
2, R
3 and R
8 are the same or different and each represents an alkyl group of 1-18 carbon atoms;
R
4, R
5, R
6, and R
7 are the same or different and each represents an alkylene group of 1-3 carbon atoms;
and R' represents an alkyl group of 1 to 4 carbon atoms.
[0039] Although the above sulfur-containing phenol derivatives are per se known as oxidation
inhibitors for plastics, the present inventors have discovered that they effectively
prevent engine oils from deteriorating.
[0040] The alkyl groups in the above formulae may be of straight chain type or branched
chain type. Examples of them include methyl, ethyl, propyl, n-butyl, isobutyl, pentyl,
isopentyl group, heptyl group, octyl group, 2-ethylhexyl, nonyl, decyl, dodecyl and
tridecyl. Particularly preferred are alkyl groups having 1-14 carbon atoms. Examples
of the alkylene group in the formulae are methylene, ethylene and propylene.
[0041] Each of the sulfur-containing phenol derivatives of the formulae (I), (11), and (III)
can be used singly or in combination with other sulfur-containing phenol derivatives.
Preferably, the sulfur-containing phenol derivative of the formula (I) is used in
combination with the sulfur-containing phenols derivative of formulae (II) or (III).
[0042] The sulfur-containing phenol derivative is generally incorporated into an engine
oil in an amount of 0.05 to 5 wt.%, preferably 0.1 to 3 wt.%, per total amount of
the engine oil.
[0043] As is described above, the sulfur-containing phenol derivative is used in combination
with a dithiophosphate such as zinc dialkyldithiophosphate or zinc dihydrocarbyldithiophosphate,
which are known oxidation inhibitors for engine oils. The preferred weight ratio is
in the range of 1:0.1-1:20, particularly 1:0.2-1:10 (= sulfur-containing phenol derivative:dithiophosphate).
DITHIOCARBAMATE COMPOUND
[0044] Preferably, the engine oil composition of the invention further contains an alkylthiocarbamoyl
compound represented by the following formula:

wherein R
9, R
10, R11 and R
12 are the same or different and each represents an alkyl group of 1-18 carbon atoms,
and (X) represents S, S-S, S-CH
2-S, S-CH
2-CH
2-S, S-CH
2-CH
2-CH
2-S or S-CH
2-CH(CH
3)-S.
[0045] The alkylthiocarbamoyl compounds of the above formula are known compounds, which
are employed as a vulcanization accelerator or an additive of gear oils and turbine
oils. The alkyl group in this formula may be of straight chain type or branched chain
type. Examples of the alkyl group are methyl, ethyl, propyl, n-butyl, isobutyl, pentyl,
isopentyl, heptyl, octyl, 2-ethylhexyl, nonyl, decyl, and dodecyl. Preferred are alkyl
groups having 1-10 carbon atoms. Concrete examples of the alkylthiocarbamoyl compounds
include methylene bis(dibutyl dithiocarbamate), bis(dimethylthiocarbamoyl)-monosulfide,
bis(dimethylthiocarbamoyl)disulfide, bis(diamylthiocarbamoyl)disulfide, and bis(dioctylthiocarbamoyl)disulfide.
Further, metal dithiocarbamates such as zinc dithiocarbamate, copper dithiocarbamate
and molybdenum dithiocarbamate are also employable. These compounds can be used singly
or in combination of two or more compounds.
[0046] The alkylthiocarbamoyl compound is generally incorporated into an engine oil in an
amount of 0.05-8 wt.%., preferably 0.1-4 wt.%, per total amount of the engine oil.
[0047] When the alkylthiocarbamoyl compound is incorporated into the engine oil of the invention,
the preferred weight ratio of the compound to the sulfur-containing phenol derivative
is in the range of 1:0.1 to 1:20, particularly 1:0.2 to 1:10 (= sulfur- containing
phenol derivative:alkylthiocarbamoyl compound).
EXAMPLES
[0048] The invention will be further illustrated by the following examples that set forth
particularly advantageous method embodiments. While the Examples are provided to illustrate
the present invention, they are not intended to limit it.
[0049] Various engine oils set forth in Table 1 were prepared from the same components such
as paraffinic mineral oil (viscosity index value: 100), viscosity index improver and
additives package (i.e., a mineral oil in which the same ashless dispersant, metal-
containing detergent and zinc dialkyldithiophosphate are dissolved), and various additives
set forth in Table 1. The viscosity of each prepared engine oil was adjusted to SAE
10W30.
[0050] 40 ml of each prepared engine oil and 2 ml of regular gasoline were mixed, and then
iron-copper catalyst (1/6 scale of the sample regulated in the oxidation test of JIS-K-2514)
was added to the mixture. The obtained mixture was heated to 140°C. At this temperature,
nitrogen gas containing 0.8% nitrogen monoxide (NO) and wet airwere continuously introduced
into the mixture at the rate of 5.7 1/hour and 151/hour, respectively. While the gases
were blowing into the engine oil, the amount of deterioration of the oil was observed
in the following manner.
[0051] The engine oil was periodically sampled and charged in an optical cell of 0.1 mm
thickness to measure IR absorption spectrum. The amount of nitrate ester formed in
the sampled oil was evaluated by the absorbance at 1630 cm-
1. The lifetime of the sampled engine oil was determined by the time when the absorbance
was reached to 0.2.

[0052] As is described above, paraffinic mineral oil (viscosity index value: 100) was used
for the engine oils set forth in Table 1 as a base oil, and each of the engine oils
was prepared to satisfy the viscosity condition regulated in SAE 10W30 of API service.
Further, other supplemental additives such as anti-foaming agents were added when
they were required. Details of the additives set forth in Table 1 are as follows:
Additives package: Mixture of boric acid-modified succinic imide (ashless dispersant),
calcium sulfonate (metal-containing detergent) and zinc dithiophosphate (of secondary
alkyl type). The weight ratio of these components is 100:40:40 in the order described.
This package, at 6.5% wt%, resulted in the phosphorus level of 0.08 wt% of engine
oil samples.
Oxidation inhibitor of amine type: Dialkyldiphenylamine
Oxidation inhibitor of phenol type: 2,6-di-t-butyl-p-cresol
Sulfur-containing phenol derivative (I): 2,4-bis{(octylthio)methyl}-o-cresol
Sulfur-containing phenol derivative (II): 2,2-thio-diethylenebis{3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate)
Sulfur-containing phenol derivative (III); Tridecyl 2-(3,5-di-t-butyl-4-hydroxybenzylthio)acetate
Dithiocarbamate compound: Methylenebis(dibutyldithiocarbamate)
[0053] As is clear from the test data set forth in Table 1, each of the engine oils of the
present invention (i.e., the engine oils of No. 4 - No. 8), in which the sulfur-containing
phenol derivative had been added, exhibited little deterioration and a long lifetime,
even if exposed to nitrogen oxide of high concentration. Particularly, the engine
oils of No. 7 and No. 8, in which the sulfur-containing phenol derivative had been
incorporated with an alkylthiocarbamoyl compound, exhibited longer lifetimes than
others.
[0054] The engine oil composition of the present invention, which is prepared by incorporating
a sulfur-containing phenol derivative to a composition of a lubricating base oil,
an ashless dispersant, a metal-containing detergent and zinc dithiophosphate, is hardly
deteriorated on contact with nitrogen oxide (NO
X) gas of high concentration and can work stably for a long time.
[0055] While the present invention has been described with reference to specific embodiments,
this application is intended to cover those various changes and substitutions that
may be made by those skilled in the art without departing from the spirit and scope
of the appended claims.
1. A low-phosphorous lubricating oil composition for internal combustion engines comprising:
(a) a major amount of a base oil of lubricating viscosity,
(b) from 0.5 to 20 wt.% of metal-containing detergent,
(c) from 0.5 to 15 wt.% of ashless dispersant,
(d) from 0.1 to 3 wt.% of zinc dithiophosphate, and
(e) from 0.05 to 5 wt.% of a sulfur-containing phenol derivative selected from the
group consisting of:


and

wherein R
1, R
2, R
3, and R
8 are the same or different and each represents an alkyl group of 1 to 18 carbon atoms;
R
4, R
5, R
6, and R
7 are the same or different and each represents an alkylene group of 1 to 3 carbon
atoms; and R' represents an alkyl group of 1 to 4 carbon atoms.
2. A low-phosphorous lubricating oil composition according to Claim 1 wherein the
sulfur-containing phenol derivative comprises 0.1 to 3 wt.% of the composition.
3. A low-phosphorous lubricating oil composition according to Claim 1 wherein the
alkyl groups of the sulfur-containing phenol derivative have 1-14 carbon atoms.
4. A low-phosphorous lubricating oil composition according to Claim 1 wherein the
alkyl groups of the sulfur-containing phenol derivative is selected from the group
consisting of 2,4-bis{(octylthio)methyl}-o-cresol, 2,2-thio-diethylenebis{3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate},
and tridecyl 2-(3,5-di-t-butyl-4-hy- droxybenzylthio)acetate.
5. A low-phosphorous lubricating oil composition according to Claim 1 wherein the
zinc dithiophosphate is a secondary alkyl type.
6. A low-phosphorous lubricating oil composition according to Claim 1 further comprising
from 0.05 to 8 wt.% of an alkylthiocarbamoyl compound represented by the formula:

wherein R
9, R
10, R
11 and R
12 are the same or different and each represents an alkyl group of 1-18 carbon atoms,
and (X) represents S, S-S, S-CH
2-S, S-CH
2-CH
2-S, S-CH
2-CH
2-CH
2-S or S-CH
2-CH(CH
3)-S.
7. A low-phosphorous lubricating oil composition according to Claim 6 wherein R9, R10, R11 and R12 are independently selected from alkyl groups having 1 to 6 carbon atoms.
8. The low phosphorous oil composition of Claim 7 wherein the dithiocarbamate compound
is methylene bis(dibutyldithiocarbamate).
9. An additive concentrate comprising:
(a) 100 weight parts of a metal-containing detergent,
(b) from 10 to 700 weight parts of an ashless dispersant, and
(c) from 2 to 200 weight parts of a sulfur-containing phenol derivative selected from
the group consisting of:


and

wherein R
1, R
2, R
3, and R
8 are the same or different and each represents an alkyl group of 1 to 18 carbon atoms;
R
4, R
5, R
6, and R
7 are the same or different and each represents an alkylene group of 1 to 3 carbon
atoms; and R' represents an alkyl group of 1 to 4 carbon atoms.
10. An additive concentrate according to Claim 9 wherein the alkyl groups of the sulfur-containing
phenol derivative have 1-14 carbon atoms.
11. An additive concentrate according to Claim 9 wherein the alkyl groups of the sulfur-containing
phenol derivative is selected from the group consisting of 2,4-bis{(octylthio)methyl}-o-cresol,
2,2-thio- diethylenebis{3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate}, and tridecyl
2-(3,5-di-t-butyl-4-hydroxyben- zylthio)acetate.