TECHNICAL FIELD OF THE INVENTION
[0001] The present invention is in the field of lubricant additives and lubricant formulations.
Specifically, the present invention relates to a boron-free lubricant additive package
that is capable of passing tests for which the presence of boron was thought to be
essential to passing.
BACKGROUND OF THE INVENTION
[0002] Historically, boron-containing lubricants have been used to attain satisfactory performance
against standard industry tests. Two such industry tests are the ISOT and the L60-1.
However, boron imparts certain undesirable properties to the lubricant such as moisture
sensitivity and increased price. Thus, it is desirable to have a lubricant that can
provide the performance demanded by industry while reducing or eliminating the presence
of boron. Recently, a boron-free lubricant additive package has been developed that
unexpectedly passes both the ISOT standard test and the L60-1 standard test.
SUMMARY OF THE INVENTION
[0003] The present invention provides a lubricating additive package that is capable of
passing both the ISOT standard test and the L60-1 standard test. More specifically,
the present invention in an embodiment provides an oil soluble lubricant additive
package comprising: (a) a succinimide dispersant, (b) an antiwear agent, (c) an extreme
pressure additive, wherein the weight ratio of said dispersant to said extreme pressure
additive is from about 1:7 to about 1:2, and wherein the package is boron-free, and
wherein the total phosphorus content of the package is not more than about 500 ppm.
[0004] In another embodiment is provided a lubricating oil comprising: (a) a base oil; and
(b) the oil soluble lubricant additive package taught herein.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT(S)
[0005] In accordance with the foregoing summary, the following presents a detailed description
of one embodiment of the invention that is currently considered to be the best mode.
[0006] We begin with a discussion of the various components employed in certain embodiments
of the present invention. Then we present a lubricant additive package of the present
invention and an example of a lubricant oil comprising the inventive lubricant additive
package. We conclude with a discussion of the L60-1 and ISOT test performance attained
by the inventive lubricant additive package.
BASE OIL
[0007] The base oils useful herein include natural lubricating oils, synthetic lubricating
oils, and mixtures thereof. Suitable lubricating oils also include basestocks obtained
by isomerization of synthetic wax and slack wax, as well as basestocks produced by
hydrocracking the aromatic and polar components of the crude. In general, both the
natural and synthetic lubricating oils will each have a kinematic viscosity ranging
from about 1 to about 40 mm
2/s (cSt) at 100° C, although typical applications will require each of the base oils
to have a viscosity ranging from about 1 to about 16 mm
2/s (cSt) at 100° C, preferably 2 to 15 mm
2/s (cSt) at 100° C.
[0008] Natural lubricating oils include animal oils, vegetable oils (e.g., castor oil and
lard oil), petroleum oils, mineral oils, and oils derived from coal or shale. The
preferred natural lubricating oil comprises mineral oil.
[0009] The mineral oils useful in this invention can include but are not limited to all
common mineral oil base stocks. This would include oils that are naphthenic or paraffinic
in chemical structure. Oils that are refined by conventional methodology using acid,
alkali, and clay or other agents such as aluminum chloride, or be extracted oils produced,
for example, by solvent extraction with solvents such as phenol, sulfur dioxide, furfural,
dichlorodiethyl ether, etc. They may be hydrotreated or hydrorefined, dewaxed by chilling
or catalytic dewaxing processes, or hydrocracked. The mineral oil may be produced
from natural crude sources or be composed of isomerized wax materials or residues
of other refining processes. In one embodiment, the oil of lubricating viscosity is
a hydrotreated, hydrocracked and/or iso-dewaxed mineral oil having a Viscosity Index
(VI) of greater than 80, preferably greater than 90; greater than 90 volume % saturates
and less than 0.03 wt. % sulfur.
[0010] Group II and Group III basestocks are also particularly suitable for use in the present
invention, and are typically prepared from conventional feedstocks using a severe
hydrogenation step to reduce the aromatic, sulfur and nitrogen content, followed by
dewaxing, hydrofinishing, extraction and/or distillation steps to produce the finished
base oil. Also useful herein are base oils known as Group III, ≤ 0.03 wt. % sulfur,
and ≥ 90 vol% saturates, viscosity index > 120; and Group IV, poly-alpha-olefins.
Hydrotreated basestocks and catalytically dewaxed basestocks, because of their low
sulfur and aromatics content, generally fall into the Group II and Group III categories.
[0011] There is no limitation as to the chemical composition of the various basestocks used
in the present invention. For example, the proportions of aromatics, paraffinics,
and naphthenics in the various Group I, Group II and Group III oils can vary substantially.
The degree of refining and the source of the crude used to produce the oil generally
determine this composition. In one embodiment, the base oil comprises a mineral oil
having a VI of at least 110.
[0012] The lubricating oils may be derived from refined, re-refined oils, or mixtures thereof.
Unrefined oils are obtained directly from a natural source or synthetic source (e.g.,
coal, shale, or tar sands bitumen) without further purification or treatment. Examples
of unrefined oils include shale oil obtained directly from a retorting operation,
petroleum oil obtained directly from distillation, or an ester oil obtained directly
from an esterification process, each of which is then used without further treatment.
Refined oils are similar to the unrefined oils except that refined oils have been
treated in one or more purification steps to improve one or more properties. Suitable
purification techniques include distillation, hydrotreating, dewaxing, solvent extraction,
acid or base extraction, filtration, and percolation, all of which are known to those
skilled in the art. Re-refined oils are obtained by treating used oils in processes
similar to those used to obtain the refined oils. These re-refined oils are also known
as reclaimed or reprocessed oils and are often additionally processed by techniques
for removal of spent additives and oil breakdown products.
[0013] Synthetic lubricating oils include hydrocarbon oils and halo-substituted hydrocarbon
oils such as oligomerized, polymerized, and interpolymerized olefins; alkylbenzenes;
polyphenyls; and alkylated diphenyl ethers, alkylated diphenyl sulfides, as well as
their derivatives, analogs, and homologs thereof, and the like. Preferred synthetic
oils are oligomers of α-olefins, particularly oligomers of 1-decene, having a viscosity
ranging from about 1 to about 12, preferably 2 to 8, mm
2/s (cSt) at 100° C. These oligomers are known as poly-α-olefins or PAOs.
[0014] Synthetic lubricating oils also include alkylene oxide polymers, interpolymers, copolymers,
and derivatives thereof where the terminal hydroxyl groups have been modified by esterification,
etherification, etc. This class of synthetic oils is exemplified by polyoxyalkylene
polymers prepared by polymerization of ethylene oxide or propylene oxide; the alkyl
and aryl ethers of these polyoxyalkylene polymers (e.g., methyl-polyisopropylene glycol
ether having an average molecular weight of 1000, diphenyl ether of polypropylene
glycol having a molecular weight of 100-1500); and mono- and poly-carboxylic esters
thereof (e.g., the acetic acid esters, mixed C
3-C
8 fatty acid esters, and C
12 oxo acid diester of tetraethylene glycol).
[0015] Another suitable class of synthetic lubricating oils comprises the esters of dicarboxylic
acids (e.g., phthalic acid, succinic acid, alkyl succinic acids and alkenyl succinic
acids, maleic acid, azelaic acid, subric acid, sebasic acid, fumaric acid, adipic
acid, linoleic acid dimer, malonic acid, alkylmalonic acids, alkenyl malonic acids,
etc.) with a variety of alcohols (e.g., butyl alcohol, hexyl alcohol, dodecyl alcohol,
2-ethylhexyl alcohol, ethylene glycol, diethylene glycol monoethers, propylene glycol,
etc.). Specific examples of these esters include dibutyl adipate, di(2-ethylhexyl)
sebacate, di-
n-hexyl fumarate, dioctyl sebacate, diisooctyl azelate, diisodecyl azelate, dioctyl
isothalate, didecyl phthalate, dieicosyl sebacate, the 2-ethylhexyl diester of linoleic
acid dimer, and the complex ester formed by reacting one mole of sebasic acid with
two moles of tetraethylene glycol and two moles of 2-ethyl-hexanoic acid, and the
like. A preferred type of oil from this class of synthetic oils is adipates of C
4 to C
12 alcohols.
[0016] Esters useful as synthetic lubricating oils also include those made from C
5 to C
12 monocarboxylic acids and polyols and polyol ethers such as neopentyl glycol, trimethylolpropane
pentaeythritol, dipentaerythritol, tripentaerythritol, and the like.
[0017] Silicon-based oils (such as the polyalkyl-, polyaryl-, polyalkoxy-, or polyaryloxy-siloxane
oils and silicate oils) comprise another useful class of synthetic lubricating oils.
These oils include tetra-ethyl silicate, tetra-isopropyl silicate, tetra-(2-ethylhexyl)
silicate, tetra-(4-methyl-2-ethylhexyl) silicate, tetra-(p-
tert-butylphenyl) silicate, hexa-(4-methyl-2-pentoxy)-disiloxane, poly(methyl)-siloxanes
and poly (methylphenyl) siloxanes, and the like. Other synthetic lubricating oils
include liquid esters of phosphorus containing acids (e.g., tricresyl phosphate, trioctylphosphate,
and diethyl ester of decylphosphonic acid), polymeric tetra-hydrofurans, poly-alpha-olefins,
and the like.
DISPERSANTS
[0018] Dispersants derived from polyisobutylene (PIB) or mixed butane-substituted succinimides
are among the succinimide dispersants useful herein, where the molecular weight range
of the PIB is approximately 900-2100, most especially MW range 1200-1500. In one embodiment,
the succinimide is malienated to a succinic anhydride to PIB ratio of approximately
1.0-1.25. The polyisobutylene succinic anhydride intermediate can be further reacted
with a suitable amine including any mono-, di-, or polyamine.
[0019] The dispersant may comprise one or more of various types of ashless dispersants including
succinimides, succinamides, succinic esters, and succinic ester-amides.
[0020] Methods for the production of the foregoing types of ashless dispersants are known
to those skilled in the art and are reported in the patent literature. For example,
the synthesis of various ashless dispersants of the foregoing types is described in
such patents as U.S. Patent Nos. 2,459,112; 2,962,442, 2,984,550; 3,036,003; 3,163,603;
3,166,516; 3,172,892; 3,184,474; 3,202,678; 3,215,707; 3,216,936; 3,219,666; 3,236,770;
3,254,025; 3,271,310; 3,272,746; 3,275,554; 3,281,357; 3,306,908; 3,311,558; 3,316,177;
3,331,776; 3,340,281; 3,341,542; 3,346,493; 3,351,552; 3,355,270; 3,368,972; 3,381,022;
3,399,141; 3,413,347; 3,415,750; 3,433,744; 3,438,757; 3,442,808; 3,444,170; 3,448,047;
3,448,048; 3,448,049; 3,451,933; 3,454,497; 3,454,555; 3,454,607; 3,459,661; 3,461,172;
3,467,668; 3,493,520; 3,501,405; 3,522,179; 3,539,633; 3,541,012; 3,542,680; 3,543,678;
3,558,743; 3,565,804; 3,567,637; 3,574,101; 3,576,743; 3,586,629; 3,591,598; 3,600,372;
3,630,904; 3,632,510; 3,632,511; 3,634,515; 3,649,229; 3,697,428; 3,697,574; 3,703,536;
3,704,308; 3,725,277; 3,725,441; 3,725,480; 3,726,882; 3,736,357; 3,751,365; 3,756,953;
3,793,202; 3,798,165; 3,798,247; 3,803,039; 3,804,763; 3,836,471; 3,862,981; 3,936,480;
3,948,800; 3,950,341; 3,957,854; 3,957,855; 3,980,569; 3,991,098; 4,071,548; 4,173,540;
4,234,435; 5,137,980 and Re 26,433, herein incorporated by reference.
[0021] In some embodiments, the ashless dispersant may comprise one or more alkenyl succinimides
of an amine having at least one primary amino group capable of forming an imide group.
The alkenyl succinimides may be formed by conventional methods such as by heating
an alkenyl succinic anhydride, acid, acid-ester, acid halide, or lower alkyl ester
with an amine containing at least one primary amino group. The alkenyl succinic anhydride
may be made readily by heating a mixture of polyolefin and maleic anhydride to about
180°-220°C. The polyolefin may be a polymer or copolymer of a lower monoolefin such
as ethylene, propylene, isobutene and the like, having a number average molecular
weight in the range of about 700 to about 2100 as determined by gel permeation chromatography
(GPC).
[0022] Amines which may be employed in forming the ashless dispersant include without limitation
any that have at least one primary amino group which can react to form an imide group
and at least one additional primary or secondary amino group and/or at least one hydroxyl
group. A few representative examples are: N-methylpropanediamine, N-dodecylpropanediamine,
N-aminopropyl-piperazine, ethanolamine, N-ethanol-ethylenediamine, N-phenylenediamine,
and the like.
[0023] Suitable amines may include alkylene polyamines, such as propylene diamine, dipropylene
triamine, di-(1,2-butylene)triamine, and tetra-(1,2-propylene)pentamine. A further
example includes the ethylene polyamines which can be depicted by the formula H
2N(CH
2CH
2NH)
nH, wherein n may be an integer from about one to about ten. These include: ethylene
diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, pentaethylene
hexamine, and the like, including mixtures thereof in which case n is the average
value of the mixture. These depicted ethylene polyamines have a primary amine group
at each end so they may form mono-alkenylsuccinimides and bis-alkenylsuccinimides.
Commercially available ethylene polyamine mixtures may contain minor amounts of branched
species and cyclic species such as N-aminoethyl piperazine, N,N'-bis(aminoethyl)piperazine,
N,N'-bis(piperazinyl)ethane, and like compounds. The commercial mixtures may have
approximate overall compositions falling in the range corresponding to diethylene
triamine to tetraethylene pentamine. The molar ratio of polyalkenyl succinic anhydride
to polyalkylene polyamines may be from about 1:1 to about 2.4:1.
[0024] In some embodiments, the ashless dispersant may comprise the products of the reaction
of a polyethylene polyamine, e.g. triethylene tetramine or tetraethylene pentamine,
with a hydrocarbon substituted carboxylic acid or anhydride made by reaction of a
polyolefin, such as polyisobutene, of suitable molecular weight, with an unsaturated
polycarboxylic acid or anhydride, e.g., maleic anhydride, maleic acid, fumaric acid,
or the like, including mixtures of two or more such substances.
[0025] The dispersant may contain at least one polyalkylene moiety. As a further example,
the dispersant, may comprise at least two polyalkylene moieties. The polyalkylene
moiety may have a molecular weight of from about 900 amu to about 3000 amu. The polyalkylene
moiety polyalkylene moiety may, for example, have a molecular weight of from about
1300 amu to about 2100 amu. As a further example, the polyalkylene moiety may have
a molecular weight of about 2100 amu. The polyalkylene moiety may comprise a polybutenyl
group.
[0026] The dispersant may be dissolved in oil of suitable viscosity for ease of handling.
It should be understood that the weight percentages given here are for neat dispersant,
without any diluent oil added.
[0027] The dispersant may be further reacted with an organic acid, an anhydride, and/or
an aldehyde/phenol mixture. Such a process may enhance compatibility with elastomer
seals, for example. The dispersant may further comprise a mixture of dispersants.
As a further example, the dispersant may comprise nitrogen and/or may be free of phosphorus.
The dispersant may be present in an embodiment in the lubricating fluid in an amount
of about 1 wt% to about 5 wt%.
[0028] The dispersant used in some embodiments of the present disclosure may comprise a
succinimide prepared from an alkenyl succinic acid or anhydride and ammonia. For example,
the succinimide may comprise the reaction product of a succinic anhydride and ammonia.
The alkenyl group of the alkenyl succinic acid may be a short chain alkenyl group,
for example, the alkenyl group may comprise about 12 to about 36 carbon atoms. Further,
the succinic anhydride may comprise a C
12 to about C
36 aliphatic hydrocarbyl succinimide. As a further example, the succinic anhydride may
comprise a C
16 to about C
28 aliphatic hydrocarbyl succinimide. As an even further example, the succinic anhydride
may comprise a C
18 to about C
24 aliphatic hydrocarbyl succinimide.
[0029] The succinimide may be prepared from a succinic anhydride and ammonia as described
in European Patent 0 020 037, herein incorporated by reference. Further, the succinimide
may comprise HiTEC® 3191 friction modifier, available from Ethyl Corporation. In some
embodiments, no non-metallic friction modifier other than the succinimide disclosed
herein is included.
[0030] The succinimide may comprise one or more of a compound having the following structure:

wherein Z may have the structure:

wherein R
1 and R
2 may be independently hydrogen or straight or branched chain hydrocarbon groups containing
from about 1 to about 34 carbon atoms such that the total number of carbon atoms in
R
1 and R
2 is from about 11 to about 35; and
wherein, in addition to or in the alternative, the succinimide may be formed by
reacting maleic acid, anhydride, or ester with an internal olefin containing about
12 to about 36 carbon atoms, said internal olefin being formed by isomerizing the
olefinic double bond of a linear α-olefin or mixture thereof to obtain a mixture of
internal olefins.
[0031] One embodiment utilizes a poly-amine of the type tetra ethyl pentamine. Examples
can include but are not limited to HiTEC® 646 Dispersant, available from Ethyl Corporation,
and similar succinimide dispersants.
EXTREME PRESSURE ADDITIVES
[0032] Extreme pressure agents known to those skilled in the art are useful in the lubricant
additive packages, lubricating oil, lubricated machines, and methods of the present
invention. Also useful herein as extreme pressure agents are sulfurized olefins, including
but not limited to sulfurized isobutylene, alkylpolysulfides and sulfurized fatty
acid esters.
CORROSION INHIBITORS
[0033] Corrosion inhibitors of the thiadiazole and triazole classes are suitable for use
in this invention. Alkyl substituted thiadiazoles as well as alkyl substituted triazoles
are useful in this invention.
OTHER AGENTS
[0034] Antiwear and siloxane-containing polymer antifoam agents, well known to those skilled
in the art and as taught in, for example, U.S. Patent No. 5,492,638, can also be employed
in the lubricant additive packages and finished lubricating oils of the present invention.
[0035] A variety of oil-soluble sulphur-containing antiwear and/or extreme pressure additives
can be used in the practice of this invention. Examples are included within the categories
of dihydrocarbyl polysulphides; sulphurized olefins; sulphurized fatty acid esters
of both natural and synthetic origins; trithiones; sulphurized thienyl derivatives;
sulphurized terpenes; sulphurized oligomers of C2 -C8 monoolefins; and sulphurized
Dieis-Alder adducts such as those disclosed in U.S. reissue patent Re 27,331. Specific
examples include sulphurized polyisobutene of Mn 1,100, sulfurized isobutylene, sulphurized
diisobutylene, sulphurized triisobutylene, dicyclohexyl polysulphide, diphenyl polysulphide,
dibenzyl polysulphide, dinonyl polysulphide, and mixtures of di-tert-butyl polysulphide
such as mixtures of di-tert-butyl trisulphide, di-tert-butyl tetrasulphide and di-tert-butyl
pentasulphide, among others.
[0036] Combinations of such categories of sulphur-containing antiwear and/or extreme pressure
agents can also be used, such as a combination of sulphurized isobutylene and di-tert-butyl
trisulphide, a combination of sulphurized isobutylene and dinonyl trisulphide, a combination
of sulphurized tall oil and dibenzyl polysulphide, and the like.
[0037] Reference should be had to EP 531 585 referred to above for further details concerning
this component.
[0038] For purposes of this invention a component which contains both phosphorus and sulphur
in its chemical structure is deemed a phosphorus-containing antiwear and/or extreme
pressure agent rather than a sulphur-containing antiwear and/or extreme pressure agent.
[0039] One such type of phosphorus- and nitrogen-containing antiwear and/or extreme pressure
additives which can be employed in the practice of this invention are the phosphorus-
and nitrogen-containing compositions of the type described in G.B. 1,009,913; G.B.
1,009,914; U.S. Pat. No. 3,197,405 and/or U.S. Pat. No. 3,197,496. In general, these
compositions are formed by forming an acidic intermediate by the reaction of a hydroxy-substituted
triester of a phosphorothioic acid with an inorganic phosphorus acid, phosphorus oxide
or phosphorus halide, and neutralizing a substantial portion of said acidic intermediate
with an amine or hydroxy-substituted amine.
[0040] Another type of phosphorus- and nitrogen-containing antiwear and/or extreme pressure
additive which can be used in the compositions of this invention is the amine salts
of hydroxy-substituted phosphetanes or the amine salts of hydroxy-substituted thiophosphetanes.
Examples of this general type of antiwear and/or extreme pressure agent include the
amine salts hydroxyphosphetanes and the amine salts of hydroxy-thiophosphetanes typified
by Irgalube 295 additive (Ciba-Geigy Corporation).
[0041] Another useful category of phosphorus- and nitrogen-containing antiwear and/or extreme
pressure agents is comprised of the amine salts of partial esters of phosphoric and
thiophosphoric acids. For further details concerning this component, reference should
be had to EP 531 585 referred to above.
[0042] The formulations of the present invention have a total phosphorus content of not
more than about 500 ppm. The formulations are also boron-free. By "boron-free" herein
is meant substantially free of boron whereby trace amounts of or contamination with
low or unintended levels of boron are to be included. Boron-free can herein include
low levels of boron up to about 25 ppm. By "substantially free of boron" herein is
meant less than about 50 ppm of boron.
[0043] NOTE: Current Boronated packages offered by Ethyl contain 125 - 150ppm of Boron.
I think the above levels are too high
EXAMPLE FORMULATION
[0044] An example of an oil soluble lubricant additive package formulation of the present
invention is outlined in the table below:
Component |
Wt % |
Sulfurized olefin |
30-50 |
Primary amine |
0.1-5 |
|
Acid phosphate |
0.5-5.0 |
Rust Inhibitor |
0.01-1 |
Antifoamant |
0.2-2.0 |
Corrosion Inhibitor |
0.2-2.0 |
|
Diluent Oil |
30-40 |
Dispersant |
2-15.0 |
[0045] A finished oil comprising the preferred boron-free oil soluble lubricant additive
package was manufactured for testing purposes. The finished oil was then tested by
the L60-1 and the ISOT standard tests. It was unexpected that a lubricant additive
package could pass both the L60-1 and ISOT standard tests without the inclusion of
a boron source in the formulation.

[0046] The L60-1 test requires at least a 7.5 carbon / varnish ( C / V) rating or higher
to pass, and at least a 9.4 sludge rating or higher to pass. The L60-1 rating is based
on a merit system with 10 indicating no carbon / varnish and zero representing the
worst rating.
[0047] The ISOT test, conversely, requires at most a 3.0 for varnish on the glass beaker
and for varnish on the glass rod to indicate clean gear performance. The ISOT rating
is based on a demerit system with the best ISOT rating zero indicating no varnish
and 9 representing the worst varnish rating. This rating may also be described as
thinly to lightly adhering lacquer in the ISOT procedure. Note that prior art formulations
containing phosphorus and boron pass both tests. Formulations with low phosphorus
alone do not pass both tests. Only the formulations of the present invention with
both low phosphorus and a dispersant pass both tests without boron.
[0048] The formulations of the present invention are especially effective in the lubrication
of vehicular axle gears and vehicular transmission gears. The vehicles can be passenger
cars, light duty trucks, heavy duty trucks, buses, recreation vehicles, marine craft,
and the like.
[0049] While the invention has been described in connection with what is presently considered
to be the most practical and preferred embodiments, it is to be understood that the
invention is not to be limited to the disclosed embodiments), but on the contrary,
is intended to cover various modifications and equivalent arrangements included within
the spirit and scope of the appended claims, which are incorporated herein by reference.
1. An oil soluble lubricant additive package including:
(a) a dispersant including no more than 500 ppm of phosphorus, wherein said dispersant
is substantially free of boron; and
(b) at least one antiwear agent, wherein the weight ratio of said dispersant to said
antiwear agent is from 10:1 to 2:1.
2. The oil soluble lubricant additive package according to claim 1, wherein said dispersant
is selected from one or more of various types of ashless dispersants including succinimides,
succinamides, succinic esters, and succinic ester-amides.
3. The oil soluble lubricant additive package according to any one of claims 1-2, wherein
at least one antiwear agent is selected from dihydrocarbyl polysulphides; sulphurized
olefins; sulphurized fatty acid esters of both natural and synthetic origins; trithiones;
sulphurized thienyl derivatives; sulphurized terpenes; sulphurized oligomers of C2
-C8 monoolefins; and sulphurized Dieis-Alder adducts.
4. The oil soluble lubricant additive package according to any one of claims 1-3, further
including at least one inhibitor, wherein the weight ratio of said inhibitor to said
dispersant is from 1:17 to 4:5.
5. The oil soluble lubricant additive package according to claim 4, wherein at least
one said inhibitor is selected from the group consisting of: corrosion inhibitors
and oxidation inhibitors.
6. The oil soluble lubricant additive package according to claim 4, wherein at least
one said inhibitor is selected from the group consisting of thiadiazoles and triazoles.
7. The oil soluble lubricant additive package according to any one of claims 1-6, further
including an extreme pressure additive, and wherein the weight ratio of said dispersant
to said extreme pressure additive is from 1:7 to 1:2.
8. The oil soluble lubricant additive package according to claim 7, wherein said extreme
pressure additive is selected from the group consisting of sulfurized olefins, sulfurized
fatty acid esters, and alkyl polysulfides.
9. A lubricating oil including:
(a) a base oil; and
(b) the oil soluble lubricant additive package of any one of claims 1-8.
10. The lubricating oil according to claim 9, wherein said lubricating oil achieves a
satisfactory score on at least one test selected from the group consisting of: ISOT
test and L60-1 test.
11. The lubricating oil according to claim 9, wherein said lubricating oil achieves a
satisfactory score on the ISOT test and L60-1 test.
12. A machine lubricated by the lubricating oil of any one of claims 9-11.
13. The machine according to claim 12, wherein said machine is selected from vehicular
axle gears and vehicular transmission gears.
14. A vehicle including the oil soluble lubricating additive package of any one of claims
1-8.
15. A method for lubricating an axle assembly, said method including the steps of:
at least partially filling said axle assembly with a lubricant including the oil soluble
lubricant additive package of any one of claims 1-8.
16. A method for lubricating at least one moving part, said method including the steps
of:
contacting at least one said moving part with a lubricant including the oil soluble
lubricant additive package of any one of claims 1-8.