2. Background of the Invention
(1) Field of the Invention
[0001] This invention relates to an engine oil composition, and more particularly to an
engine oil composition useful as a lubricating oil for gasoline engine, diesel engine,
and the like.
(2) Description of the Prior Art
[0002] Because of increased concern regarding the energy-saving measures to counter oil
shocks, the research for a fuel-saving internal combustion engine lubricating oil
has been recently intensified. As measures for fuel-saving by use of lubricating oil
to meet such situation, the following measures are now under review among business
circles: (a) Lowering viscosity of lubricating oil with the intension of reducing
engine friction loss under hydrodynamic lubricating conditions, and (b) Addition of
friction reducers with the intension of reducing engine friction loss under mixed
and boundary lubrication.
[0003] Addition of friction modifiers to lubricating oil is indispensable especially in
latest fuel-saving lubricating oil, and many compounds have been heretofore been found
to be useful. However, it has been observed that even though these compounds possess
a high fuel-saving effect on the fresh lubricating oil, they gradually lose said effect
in the aged lubricatng oil due to degradation during engine operation. While many
antioxidants have widely been used heretofore and proved to be effective to some extent
for preventing the degradation, they could not necessarily provide satisfactory results
in view of their lubricating performance.
[0004] The present invention is based on a discovery whereby excellent fuel-saving effect
can be attained employing an overbasic metallic detergent prepared by use of an alkaline-earth
metal borate as an additional component of an engine oil composition containing a
friction modifier and an antioxidant.
[0005] The present invention provides an engine oil composition having a specific combination
of lubricating additives and excellent fuel-saving effect over a long period of time.
3. Summary of the Invention
[0006] It is an object of the subject invention to provide a fuel-saving engine oil composition
comprising a lubricating base oil and
(a) about 0.01 to 30 % by weight of an overbasic oil-soluble metal salt,
(b) about 0.01 to 5 % by weight of a friction modifier,
(c) about 0.01 to 5 % weight of an antioxidant as essential components, on the basis
of the total amount of the composition.
4. Detailed Description of the Invention
[0007] Either mineral oils or synthetic oils may be used as the lubricating base oils of
the instant invention. Any paraffinic or naphthenic lubricating base oils may be acceptable
wherein said base oils are manufactured by a process consisting mainly of topping
crude oil followed by vacuum distillation to give a lubricating oil fraction, and
refining said lubricating fraction by a process selected from the group consisting
of solvent deasphalting, solvent extraction, hydro-cracking, solvent dewaxing, catalytic
dewaxing, hydro-refining, sulfuric acid treating, and clay treating.
[0008] The synthetic oils of the present invention include, α-olefin polymers (polybutenes,
octene-1 oligomers, decene-1 oligomers, and the like), alkylbenzenes, alkylnaphthalenes,
diesters (ditridecyl glutarate, di-2-ethylhexyl adipate, diisodecyl adipate, ditridecyl
adipate, di-3-ethylhexyl sebacate, and the like), polyol esters (trimethylolpropane
caprilate, trimethylolpropane pelargonate, pentaerythritol- 2-ethyl hexanoate, pentaerythritol
pelargonate, and the like), polyoxyalkylene glycol, polyphenyl ether, silicon oils,
perfluoroalkyl ethers, and mixtures thereof.
[0009] Preferred kinematic viscosity of these lubricating base oils is in a range of about
3 to 20 cSt at 100°C.
[0010] The overbasic oil-soluble metal salts (a) of the present invention are prepared by
a reaction of an oil-soluble metal salt such as an oil-soluble alkaline-earth metal
sulfonate, alkaline-earth metal saricylate, alkaline-earth metal pheneate, alkaline-earth
metal phosphonate with an oxide or hydroxide of an alkaline-metal in the presence
of boric acid or boric acid anhydride. Among oil-soluble metal salts, alkaline-earth
metal saricylates are most appropriate. Generally, the overbaic oil-soluble metal
salts (a) of the present invention have a total base number of about 100 or more,
and preferably 170 or more, and a particle size of less than about 0.1 µm, and preferably
less than about 0.05 µm.
[0011] Any methods for preparing the overbasic metal salts may be acceptable. For example,
a method has been known which comprises reacting an oil-soluble metal salt aforesaid,
a hydroxide or an oxide of alkaline-earth metal, and boric acid or boric acid anhydride
in the presence of water, an alcohol such as methanol, ethanol, propanol, or butanol,
and a diluent such as benzene, toluene or xylene at a temperature of about 20 to 200
°C for about 2 to 8 hours, heating the mixture at about 100 to 200 °C to remove water,
followed by removing the alcohol and the diluent if necessary, to give a overbasic
metal salt. The reaction conditions may be employed suitably depending on raw material
type, the amount of reactants and the like. Typical of such prior art practices are
those disclosed in Japanese patent Publication Nos. 116688 /60 and 204298 /61 and
the disclosures of which are incorporated by reference.
[0012] A content of the overbasic metal salt prepared by use of an alkaline-earth metal
borate of the present invention is in an amount of about 0.01 to 30 % by weight, and
preferably about 0.05 to 5 % by weight, on the basis of the total amount of the composition.
[0013] The content of less than about 0.01 % by weight is not preferable because of the
insufficient display of the fuel-saving effect of the overbasic metal salt wherein
the effect can not be maintained over a long period of time. Inversely, when it is
in excess of about 30 % by weight, there is no additional merits due to the excessive
addition. Other overbasic oil-soluble metal salts, such as those prepared by use of
alkaline-earth-metal carbonates can not provide an engine oil composition which can
persistently maintain the fuel-saving effect throughout the engine operation.
[0014] Any friction modifiers (b) which have been used in conventional engine oils may be
employed in the present invention. Such modifiers,for example, include molibdenum
dithiophosphates, molibdenum dithiocarbamates, molibdenum disulfides, fluorocarbons,
boric acid esters, alkylamines, higher alcohols, higher fatty acids, fatty acid esters,
fatty acid amides and the like.
[0015] Typical friction modifiers include molybdenum sulfide diethyldithiophosphate, molybdenum
sulfide dipropyldithiophosphate, molybdenum sulfide dibutyldithiophosphate, molybdenum
sulfide dipentyldithiophosphate, molybdenum sulfide dihexyldithiophosphate, molybdenum
sulfide dioctyldithiophosphate, molybdenum sulfide didecyldithiophosphate, molybdenum
sulfide didodecyldithiophosphate, molybdenum sulfide di(butylphenyl) dithiophosphate,
Molybdenum sulfide di(nonylphenyl) dithiophosphate, oxymolybdenum sulfide diethyldithiophosphate,
oxymolybdenum sulfide dipropyldithiophosphate, oxyolybdenum sulfide dibutyldithiophosphate,
oxymolybdenum sulfide dipentyldithiophosphate, oxymolybdenum sulfide dihexyldithiophosphate,
oxymolybdenum sulfide dioctyldithiophosphate, oxymolybdenum sulfide didecyldithiophosphate,
oxymolybdenum sulfide didodecyldithiophosphate, oxymolybdenum sulfide di(butylphenyl)
dithiophosphate, oxymolybdenum sulfidedi(nonylphenyl) dithiophosphate, molybdenum
sulfide diethyldithiocarbamate, molybdenum sulfide diethyldithiocarbamate, molybdenum
sulfide dipropyldithiocarbamate, molybdenum sulfide dibutyldithiocarbamate, molybdenum
sulfide dipentyldithiocarbamate, molybdenum sulfide dihexyldithiocarbamate, molybdenum
sulfide dioctyldithiocarbamate, molybdenum sulfide didecyldithiocarbamate, molybdenum
sulfide didocecyldithiocarbamate, molybdenum sulfide di(butylphenyl) dithiocarbamate,
molybdenum sulfide di(nonylphenyl) dithiocarbamate, oxymolybdenum sulfide diethyldithiocarbamate,
oxy molybdenum sulfide diethyldithiocarbamate, oxymolybdenum sulfide dipropyldithiocarbamate,
oxymolybdenum sulfide dibutyldithiocarbamate, oxymolybdenum sulfide dipentyldithiocarbamate,
oxymolybdenum sulfide dihexyldlthiocarbamate, oxymolybdenum sulfide dioctyldithiocarbamate,
oxymolybdenum sulfide didecyldithiocarbamate, molybdenum sulfide didocecyldithiocarbamate,
oxymolybdenum sulfide di(butylphenyl) dithiocarbamate, oxymolybdenum sulfide di(nonylphenyl)
dithiocarbamate, lauryl amine, myristyl amine, palmitic amine, stearyl amine, oleyl
amine, lauryl alcohol, myristyl alcohol, palmitic alcohol, stearyl alcohol, oleyl
alcohol, lauric acid, myristic acid, palmitic acid, stearic aid, oleic acid, methyl
laurate, methyl myristate, methyl palmitate, methyl stearate, methyl oleate, lauryl
amide, myristyl amide, palmitic amide, stearyl amide, oleyl amide.
[0016] A content of the friction reducer (b) of the present invention is in an amount of
about 0.01 to 5 % by weight, and preferably about 0.05 to 2 % by weight, on the basis
of the total amount of the composition.
[0017] The content of less than about 0.01 % by weight is not preferable because of the
insufficient display of the friction reducing effect. Inversely, when it is in excess
of about 5 % by weight, there is no additional merits due to the excessive addition.
[0018] Any antioxidants (c) may be employed which have been used in conventional engine
oils. Such antioxidants, for example, include phenol type, amine type, sulfur type,
zinc thiophosphate type, phenothiazine type antioxidants, and the like. Typically,
they include diphenylamine, p,p'-dioctyl diphenylamine, p,p'-dinonyl diphenylamine,
p,p' -didodecyl diphenylamine, phenyl- α-naphthylamine, p-octylpenyl- α-naphthylamine,
p-nonylphenyl-α-naphthylamine, p-dodecylpheny- α-naphthylamine, 2,6-di-tert.-butylphenol,
2,6-di-tert.-butyl-p-cresol, 2,6-di-tert.-butyl-4-ethylphenol, 2,2'-methylenebis (4-methyl-6-tert.-butylphenol),
2,2'-methylenebis (4-ethyl-6-tert.-butylphenol), 4,4'-methylenebis (2,6-di-tert.-butylphenol),
4,4'-bis (2,6-di-tert.-butylphenol), 4,4'-thiobis (6-tert.-butyl-o-dresol, zinc dialkyl
dithiophosphate, phenotiazine, and mixtures thereof.
[0019] A content of the antioxidant (c) of the present invention is in an amount of about
0.01 to 5 % by weight, and preferably about 0.1 to 2 % by weight, on the basis of
the total amount of the composition.
[0020] The content of less than about 0.01 % by weight is not preferable because of the
display of the antioxidation effect for a short period of time. Inversely, when the
amount is in an excess of about 5 % by weight, there is no additional merits due to
the excessive addition.
[0021] In the present invention, the following conventional lubricating oil additives can
be additionally used to improve further the performance of the present composition
if necessary, in so far as they do not deviate from the gist of the present invention.
Examples of these additives include extreme pressure additives such as tricresyl phosphate,
triphenyl phosphate, zinc dithiophosphates,; rust preventives such as petroleum sulfonates,
dinonyl naphthalene sulfonates and the like; metal deactivating agents such as benzotriazole
and the like; metal-based detergents such as alkaline-earth metal sulfonates, alkaline-earth
metal salicylates, alkaline-earth metal pheneates, alkaline-earth metal phosphonates
and the like; ashless dispersants such as succinimide, succinic esters, benzylamine
and the like; deformers such as silicon oils and the like; viscosity index improvers
and pour point depressants such as polymethacrylates, polyisobutylenes and polystyrenes
and the like; and mixture thereof.
[0022] Generally, a content of the viscosity index improver is in an amount of about 1 to
30 % by weight, the deformer is in an amount of about 0.0005 to 1 % by weight, the
metal deactivating agent is in an amount of about 0.005 to 1 % by weight, and other
additives are in amounts of about 0.1 to 15 % by weight respectively on the basis
of the total amount of the composition.
[0023] The engine oil compositions of the present invention are suitable for two cycle and
four cycle gasoline engine oils, diesel engine oil for land use, marine diesel engine
oil, and the like.
[0024] While the advantages of the compositions according to the present invention will
be described in detail hereinbelow in conjunction with the following examples, it
is to be noted that the scope of the present invention should not be limited to these
examples.
Examples and Comparative Examples
[0025] According to the composition indicated in Table 1, the engine oil compositions of
the present invention were prepared. Performance tests were conducted with respect
to these compositions by the following method.
(LFW friction test)
[0026] LFW friction test is carried out on both oxidation degraded samples and freshly prepared
samples. The test conditions are as follows:

[0027] The oxidation degraded sample oils were prepared by oxidizing new sample oils under
the following conditions on the basis of " the method for testing oxidaton stability
of lubricating oil" prescribed by JIS K 2514 3.1:
- Temperature
- 150 °C
- Duration
- 72 hours
[0028] Table 1 shows the test results.
[0029] As is apparent from the results shown in Table 1, the engine oil compositions according
to the present invention have excellent performance as an engine oil in which the
fuel-saving effect can be maintained persistently throughout the engine operation
because of the synergism of each component.
[0030] On the contrary, when the compositions of Comparative Examples 1 and 2 in which an
overbasic oil-soluble metal salt prepared by use of calcium carbonate instead of an
overbasic oil-soluble metal salt (a) prepared by use of an alkaline-earth metal borate
is used, or an antioxidant of component (c) of the present invention is omitted, are
compared with those of Example respectively, the friction coefficient increases after
oxidation degradation in both cases, and the time during which the fuel-saving effect
may be maintained is shorter in both cases.
