Background of the Invention
(1) Field of the Invention
[0001] This invention relates to a method for the lubrication of an alcohol-based fuel engine,
and more particularly to a method for the lubrication of a methanol- or ethanol-based
fuel engine.
(2) Description of the Prior Art
[0002] In alcohol-based fuel engines, for example, methanol-based fuel engines, highly polar
oxidation products of alcohol such as formic acid and water are easily formed. A problem
associated with the formation of such oxidation products has been the blowing of the
products through the crankcase as a blow-by gas thus causing the crankcase to corrode
and rust. Furthermore, these polar substances are the cause of wear of several parts
of an engine, especially on the cylinder surfaces. Therefore, it is necessary to neutralize
the formic acid immediately after it contacts with or is absorbed into the engine
oil thereby deactivating the acid. For this purpose, an overbasic detergent prepared
by the use of calcium carbonate has been used in conventional engine oils in order
to lubricate alcohol-based fuel engines. However, the capacity of such a conventional
overbasic detergent for neutralizing formic acid is insufficient, and said detergent
has a tendency to form coarse-grained particles during use. Furthermore, its wear
resistance is also unsatisfactory.
[0003] It is an object of the present invention to overcome the problems inherent in the
lubrication of alcohol-fueled engines and especially methanol- or ethanol-fueled engines,
such problems originating from the specific properties of said alcohols, like a single
boiling point (whereas gasoline for engines usually has a boiling point range of from
about 30°C to about 200°C), a low vapour pressure and a high heat energy necessary
for evaporation so that methanol is nearly introduced as a liquid phase into the cylinder(s).
Furthermore, said alcohols are not soluble in oil but easily soluble in water.
[0004] The present invention is based on extensive research whereby the inventors unexpectedly
have found that efficient results can be attained by employing an overbasic alkaline-earth
metal borate, as defined in claim 1, instead of the conventional overbasic detergents
for the lubrication of alcohol-based fuel engines.
[0005] By carrying out such lubrication with an engine oil composition containing an overbasic
detergent in the form of an alkaline-earch metal borate there will be provided an
improved capacity for neutralizing formic acid, an improved wear resistance, and the
tendency to form coarse-grained particles during use will be eliminated.
[0006] It is already known from DE-A1-3 607 887 to prepare alkaline-earth metal borate dispersions
derived from oil soluble neutral sulfonates of an alkaline-earth metal, such dispersions
having a very small particle size and a high molecular ratio of borate to alkali-earth
metal.
[0007] Additionally FR-A1-2 554 825 discloses oil soluble reaction products prepared from
alkaline-earth metal salts of an organic acid, having been made basic by a pre-reaction
with CO₂ , and a boron compound like boric acid. Since such reaction products do not
comprise solid materials they can be easily compounded with luboils.
Summary of the Invention
[0008] The present invention provides a method for the lubrication of alcohol-based fuel
engines characterized by lubricating said engines with an engine oil composition containing
a major amount of mineral oil and/or synthetic oil as lubricating base oil, and 0.01
to 10% by weight of an overbasic alkaline-earth metal borate as defined in claim 1,
on the basis of the total amount of the composition as an essential component.
Detailed Description of the Invention
[0009] Either mineral oils or synthetic oils may be used as the lubricating base oils in
the present invention. Any paraffinic or naphthenic lubricating base oils may be acceptable,
said base oils being manufactured by a process consisting mainly of topping a 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. The synthetic oils used
according to the present invention include, for example, 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,
perfluoralkyl ethers, and mixture thereof.
[0010] The preferred kinematic viscosity of these lubricating base oils is in the range
of about 3 to 20.10⁻⁶ m²/s (cSt) at 100°C.
[0011] Alkaline-earth metal borates useful for the present invention have the general formula
of M O .x B₂ O₃ wherein M is an alkaline-earth metal atom, x is a positive number
having a value of 0.5 to 3.0. The alkaline-earth metals include magnesium, calcium,
barium, with calcium being preferred. The alkaline-earth metal borates have a particle
size of less than about 0.1 µm, preferably less than about 0.05 µm. The overbasic
alkaline-earth metal borates are hereinafter referred to as "alkaline-earth metal
borate dispersions". The overbasic alkaline-earth metal borate dispersions have a
total base number (measured by the procedure presribed by JIS K 2501 5.2.3) of more
than 100, preferably more than 170. The overbasic alkaline-earth metal borate dispersions
are prepared by the reaction of an oil-soluble alkaline-earth metal salicylate with
an oxide or a hydroxide of an alkaline-earth metal in the presence of boric acid or
boric acid anhydride. Any methods for preparing the overbasic alkaline-earth metal
borate dispersions may be acceptable. For example, a method has been described which
comprises reacting an oil-soluble alkaline-earth metal salicylate, 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 dispersion. The reaction
conditions may be employed suitably depending on the raw materials to be used, 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. In general, the alkaline-earth
metal borate dispersions obtained by the above-mentioned procedures have a particle
size of less than 0.1µm and a total base number of more than about 100, and are appropriate
for the present invention.
[0012] The alkaline-earth metal borate is present in the composition to be used according
to the invention in an amount of 0.01 to 10% by weight, preferably 0.05 to 3% by weight,
more preferably of about 0.05 to 1% by weight on the basis of the total amount of
the composition.
[0013] When the content is less than about 0.01% by weight, there is not observed any beneficial
effect of the alkaline-earth metal borate. Inversely, when it is in excess of 10%
by weight, the amount of sulfated ash is increased and therefore such an embodiment
is not preferred.
[0014] 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. Examples of these additives include oiliness improvers such as higher
alcohols, higher fatty acids, esters and the like; extreme pressure agents and friction
modifiers such as tricresyl phosphate, triphenyl phosphate, zinc dithiophosphates,
molybdenum disulfides, molybdenum dithiophosphates, molybdenum dithiocarbamates and
the like; 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; defoamers
such as silicon oils and the like; viscosity index improvers and pour point depressants
such as polymethacrylates, polyisobutylenes and polystyrenes and the like; antioxidants
such as zinc dithiophosphates, hindered phenols, aromatic amines and the like; and
mixtures thereof. The viscosity index improver may be present in an amount of about
1 to 30% by weight, the defoamer in an amount of about 0.0005 to 1% by weight, the
metal deactivating agent in an amount of about 0.005 to 1% by weight, and other additives
in an amount of about 0.1 to 15% by weight respectively on the basis of the total
amount of the composition.
[0015] The engine oil compositions used for the lubrication of alcohol-based fuel engines
according to the present invention are suitable for spark-ignition or compression-ignition
engines in which said alcohol-based fuel is selected from the group consisting mainly
of methanol, ethanol, propanol, mixtures thereof , and the mixture of at least 10%
by volume of one of these alcohols with a petroleum-based fuel such as gasoline, kerosene,
and gas oil.
[0016] While the advantages of the lubrication method 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 1 - 2 and Comparative Examples 1 - 2
[0017] In order to measure the capacity for neutralizing formic acid when using the present
lubrication method, engine oil compositions were prepared by blending an overbasic
oil-soluble salt prepared by use of calcium borate in an amount shown in Table 1 with
a refined mineral oil (SAE 30, 10.0 cSt (10.10⁻⁶m²/s) @ 100°C). Formic acid in an
amount shown in Table 1 was added individually to these compositions and the pH values
of these compositions after 30 sec. were measured. Table 1 gives the results.For reference,
the same procedures were repeated except that calcium carbonate was used to prepare
the overbasic oil-soluble metal salt, and the results are also shown in Table 1.

Examples 3 to 5 and Comparative Examples 3 - 5
[0018] In order to measure the wear resistance of the compositions used acording to the
invention, engine oil compositions were prepared by blending 2% by weight, on the
basis of the total amount of the composition, of overbasic oil-soluble metal salt
prepared by use of calcium borate with a refined mineral oil (SAE 10, 4.3 cSt (4.3
x 10⁻⁶m²/s) at 100°C). The tests were carried out by the high-speed four point ball
method. The test conditions were as follows:
| Test load |
Engine speed |
Test duration |
| 30 kg |
1200 r.p.m. |
30 min. |
[0019] Table 2 shows the test results. For reference, the same procedures were repeated
except that calcium carbonate was used to prepare the overbasic oil-soluble metal
salt, and the results are also shown in Table 2.

Examples 6 - 8 and Comparative Examples 6 - 8
[0020] In order to measure the stability for hydrolysis of the compositions used according
to the invention, the engine oil compositions were prepared by blending 15% by weight,
on the basis of the total amount of the composition, of an overbasic oil-soluble metal
salt prepared by use of calcium borate with a refined mineral oil (SAE 10, 4.3 cSt
(4.3 x 10⁻⁶ m²/s) at 100°C). The tests were carried out by the method prescribed by
ASTM D 2619. Table 3 gives the test results. For reference, the same procedures were
repeated except that calcium carbonate was used to prepare the overbasic oil-soluble
metal salt, and the results are also shown in Table 3.

[0021] As is apparent from the results shown in Tables 1 to 3, the engine oil compositions
for alcohol-based fuel engines used according to the present invention are superior
to the prior art of compositions for alcohol-based fuel engines in respect of capacity
for neutralizing formic acid, wear resistance, and stability against hydrolysis.
1. A method for the lubrication of an alcohol-based fuel engine comprising lubricating
said engine with an engine oil composition comprising a major amount of mineral oil
and/or synthetic oil as a lubricating base oil, and 0,01 to 10% by weight of an overbasic
alkaline-earth metal borate prepared by a reaction of an alkaline-earth metal salicylate
with an oxide or a hydroxide of an alkaline-earth metal in the presence of boric acid
or boric acid anhydride, on the basis of the total amount of the composition as an
essential component.
2. A method according to claim 1 in which said lubricating base oil comprises an overbasic
alkaline-earth metal borate dispersion with a total base number (measured according
to JISK 2501 5.2.3) of more than 100, preferably more than 170.
3. A method according to claim 1 and /or 2 in which said alkaline-earth metal borate
has a particle size of less than 0,1 µm, preferably of less than 0,05 µm.
4. A method according to anyone of the claims 1 to 3 in which said alcohol-based fuel
comprises at least 10% by volume of alcohol.
1. Ein Verfahren zum Schmieren eines Motors für einen Treibstoff auf Alkoholbasis, umfassend
das Schmieren des besagten Motors mit einer Motorölzusammensetzung, umfassend eine
größere Menge an Mineralöl und/oder synthetischem Öl als ein Basisschmieröl und als
eine wesentliche Komponente 0,01 bis 10 Gew%, bezogen auf die Gesamtmenge der Zusammensetzung,
eines überbasischen Erdalkalimetallborats, hergestellt durch eine Reaktion zwischen
einem Erdalkalimetallsalicylat und einem Oxid oder einem Hydroxid eines Erdalkalimetalls
in Gegenwart von Borsäure oder Borsäureanhydrid.
2. Ein Verfahren nach Anspruch 1, in welchem das besagte Basisschmieröl eine Dispersion
eines überbasischen Erdalkalimetallborats mit einer Gesamthasenzahl (gemessen nach
JISK 2501 5.2.3) von mehr als 100, vorzugsweise von mehr als 170, umfaßt.
3. Ein Verfahren nach Anspruch 1 und/oder 2, in welchem das besagte Erdalkalimetallborat
eine Teilchengröße von weniger als 0,1 µm, vorzugsweise von weniger als 0,05 µm, aufweist.
4. Ein Verfahren nach einem der Ansprüche 1 bis 3, in welchem der besagte Treibstoff
auf Alkoholbasis mindestens 10 Vol% Alkohol umfaßt.
1. Méthode pour lubrifier un moteur à carburant à base d'alcool comprenant la lubrification
dudit moteur avec une composition lubrifiante pour moteurs comprenant une quantité
majoritaire d'huile minérale et/ou d'huile synthétique comme huile lubrifiante de
base, et comme composant essentiel, de 0,01 à 10 % en masse, pourcentages calculés
sur la base de la quantité totale de la composition, d'un borate de métal alcalino-terreux
surbasique préparé en faisant réagir un salicylate de métal alcalino-terreux avec
un oxyde ou un hydroxyde de métal alcalino-terreux en présence d'acide borique ou
d'anhydride borique.
2. Méthode selon la revendication 1 dans laquelle ladite huile lubrifiante de base comprend
une dispersion de borate de métal alcalino-terreux surbasique avec un indice de base
totale (mesuré selon la norme JISK 2501 5.2.3) de plus de 100, de préférence de plus
de 170.
3. Méthode selon la/les revendications 1 et/ou 2 dans laquelle ledit borate de métal
alcalino-terreux a une grosseur de particule de moins de 0,1 µm, de préférence de
moins de 0,05 µm.
4. Méthode selon l'une quelconque des revendications 1 à 3 dans laquelle ledit carburant
à base d'alcool comprend au moins 10 % en volume d'alcool.