[0001] The present invention relates to novel lubricating compositions containing molybdenum
which exhibit reduced copper corrosion activity. The compositions comprise organomolybdenum
compounds and a sulfur donor compound which has been treated with a plant oil to remove
active sulfur. The molybdenum compounds used are dithiocarbamates in various forms.
BACKGROUND OF THE INVENTION
[0002] It is by now well known to use organomolybdenum compounds in lubricating oil compositions
to decrease friction between moving parts. In oils used to lubricate internal combustion
engines lowering of friction between moving parts increases fuel efficiency. As well
as oils for internal combustion engines, organomolybdenum compounds may also be used
in functional fluids such as manual and automatic transmission fluids, wet brakes
fluids, hydraulic fluids and other comparable fluids.
[0003] The organomolybdenum compounds used in lubricating compositions are molybdenum containing
alkyl and dialkyl dithiocarbamates and their oxyo and/or sulfurized analogs. Examples
of such organomolybdenum compounds are disclosed in the following patent publications,
all of which are incorporated herein by reference.
[0004] Japanese Patent Laid-Open Application No. 56202/1973 teaches a compound having the
general formula [R
2N-CS
2]
2-Mo
2S
4 wherein R is an alkyl group, which compound is useful as an additive for lubricants.
But that compound has a corrosive action on copper-containing materials, so the use
of that compound has been limited.
[0005] Japanese Patent Laid-Open No. 62-81396, for example, proposes a molybdenum-containing
lubricant additive with an excellent oxidation preventive function, wear proofing
function, friction mitigating function and metal corrosion inhibiting function, and
further is highly soluble in a base oil such as mineral oil. Japanese Patent Laid-Open
No. 48-56202 proposes an extreme pressure lubricant containing MoDTC blended thereto.
[0006] Further, Japanese Patent Laid-Open No. 5-279686 proposes a lubricating oil composition
for an internal combustion engine prepared by blending (a) sulfurized oxymolybdenum
dithiocarbamate and/or sulfurized oxymolybdenum organophosphorodithioate, (b) fatty
acid ester and/or organoamide compound, (c) at least one compound selected from the
group consisting of calcium sulfonate, magnesium sulfonate, calcium phenate and magnesium
phenate, (d) at least one compound selected from the group consisting of benzylamine
and boron derivatives of benzylamine, and (e) zinc dithiophosphate and/or zinc dithiocarbamate,
in a base oil for a lubricating oil.
[0007] Japanese Patent Laid-Open No. 5-230485 proposes a lubricating oil composition for
an engine oil containing, as essential components in a base oil using a mineral oil
and/or a synthetic lubricating of (a) an alkaline earth metal salt of alkyl-salicylic
acid, (b) a bis-type alkenylsuccinic acid imide having a polybutenyl group and/or
its derivative, and (c) sulfurized oxymolybdenum organophosphorodithioate and/or molybdenum
dithiocarbamate.
[0008] Japanese Patent Laid-Open No. 5-186787 proposes a lubricating oil composition prepared
by blending (a) sulfurized oxymolybdenum dithiocarbamate and/or sulfurized oxymolybdenum
organophosphorodithioate and (b) zinc dithiophosphate and/or zinc dithiocarbamate
into a mineral oil, and further proposes a lubricating oil composition prepared by
adding (c) an organic amide compound to the above.
[0009] Japanese Patent Laid-Open No. 5-163497 proposes an engine oil composition comprising
(A) a base oil consisting of a mineral oil and/or a synthetic oil, (B) a boron compound
derivative of alkenylsuccinic acid amide, (C) an alkaline earth metal salt of salicylic
acid and (D) molybdenum dithiophosphate and/or molybdenum dithiocarbamate, as the
principal components.
[0010] A molybdenum dihydrocarbyldithiocarbamate compound useful as an additive for lubricants
is disclosed in U.S. Patent No. 4,098,705 to Sakurai et al. Novel sulfur and phosphorus
containing molybdenum compositions which are useful for improving fuel economy for
internal combustion engines are disclosed in U.S. Patent No. 4,289,635 to Schroeck.
[0011] U.S. Patent to NTN Corporation of Japan recites a grease composition for constant
velocity joints comprising a urea grease including a lubricating oil and a urea base
thickener and containing (A) 1-5% by weight of molybdenum sulfide dialkyldithiocarbamate,
(B) 0.2-1% by weight of molybdenum disulfide, (C) 0.5-3% by weight of an extreme pressure
additive of zinc dithiophosphate and (D) 0.5-5% by weight of an oiliness agent composed
of at least one of vegetable oils and fats as an essential component, provided that
a weight ratio of the component (B) to the component (A) is 0.04-0.5.
[0012] The instant invention does not contain a urea base thickener or molybdenum disulfide.
[0013] U.S. Patent No. 5,627,146 to Asaki Denka Kogyo describes alkyl group asymmetric molybdenum
dithiocarbamate having increased oil solubility.
[0014] International patent application published under publication number WO 96/06904 to
the Tonen Corporation describes a composition having good lubricity and comprising
a major amount of a lubricant base oil, a basestock of lubricating viscosity, to which
a minor amount of additives has been added. The additives comprise specific amounts
of oxymolybdenum dithiocarbamate sulfide having specific alkyl groups, zinc dialkyldithiophosphate
having specific alkyl groups, one or more specific sulfur containing compounds, an
ashless dispersant and a boron containing additive which may be the ashless dispersant.
In further aspects of the invention a metal detergent is used. Conveniently, the dispersant
and boron are added as a borated succinimide.
[0015] The invention of WO 96/06904 is a lubricant composition comprising a major amount
of a lubricant base oil having added thereto a minor amount of additives comprising
(A) oxymolybdenum dithiocarbamate sulfide having alkyl groups with 8 to 18 carbon
atoms, (B) zinc dialkyldithiophosphate having primary alkyl groups with 1 to 18 carbon
atoms, (C) one or more additional peroxide decomposing sulfur compounds, (D) an ashless
dispersant, and (E) a boron containing additive in an amount sufficient to provide
at from 0.005 to 0.06% by weight boron to the finished lubricant wherein to the total
weight of the composition, the molybdenum content from oxymolybdenum dithiocarbamate
sulfide is at 200 to 2,000 ppm (ratio by weight); the phosphorus content from zinc
dialkyldithiophosphate is at 0.02 to 0.15% by weight; and the sulfur content from
the additional peroxide decomposing sulfur compound is at 0.02 to 0.30% by weight.
Conveniently, the additional peroxide decomposing sulfur compound is selected from
the group consisting of zinc dialkyldithiocarbamate, copper dialkyldithiocarbamate
or nickel dialkyldithiocarbamate wherein the dialkyldithiocabamate has alkyl groups
with 2 to 18 carbon atoms, bis(dialkyldithiocarbanoyl)disulfide having an alkyl group
with 2 to 18 carbon atoms, disulfide having an alkyl group with 2 to 18 carbon atoms,
disulfide having an allyl group, an alkylallyl group or an allylalkyl group with 6
to 18 carbon atoms, olefin sulfide, fish oil sulfide, whale oil sulfide and mixtures
of any of the foregoing.
[0016] WO 96/06904 describes in detail the use of additional sulfur compounds in the compositions
described.
[0017] The additional sulfur compound required by WO 96/06904 is selected from any of the
sulfur compounds that efficiently decompose peroxides. Without intending to be bound
by any theory, the extended fuel economy performance of the present invention may
be attributable to suppressed consumption of the oxymolybdenum dithiocarbamate sulfide
and the zinc dialkyldithiophosphate because the sulfur compounds efficiently decompose
peroxides.
[0018] As the dialkyldithiocarbamate salt to be blended in the lubricant composition of
the invention, use is made of a compound represented by the general formula (3)

wherein M represents zinc, copper or nickel; R
9, R
10, R
11 and R
12 may be the same or different, each representing an alkyl group with 2 to 18 carbon
atoms. Metal salts of dialkyldithiocarbamic acid are well known and readily available.
Processes for their synthesis are described in U.S. Patents 4,623,473 and 4,740,322.
[0019] The alkyl group of 2-18 carbon atoms represented by R
9, R
10, R
11 and R
12 in the general formula (3) may be linear or branched, including for example, an ethyl
group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group,
nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl
group, pentadecyl group, hexadecyl group, heptadecyl group and octadecyl group.
[0020] As the bis(dialkyldithiocarbamoyl)disulfide to be blended in the lubricant composition
of the present invention, use may be made of a compound represented by the general
formula (4):

wherein R
13, R
14, R
15 and R
16 may be the same or different, each representing an alkyl group with 2 to 18 carbon
atoms. The alkyl group of 2-8 carbon atoms represented by R
13, R
14, R
15 and R
16 in the general formula (4) may, be linear or branched, including for example an ethyl
group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group,
nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl
group, pentadecyl group, hexadecyl group, heptadecyl group and octadecyl group.
[0021] As the disulfide to be blended in the lubricant composition of the invention. use
is made of a compound represented by the general formula (5):
R
17―S―S―R
18 (5)
wherein R
17 and R
18 may be the same or different, each representing an alkyl group with 2 to 18 carbon
atoms or an allyl group, an alkylallyl group or an allylalkyl group, with 6 to 18
carbon atoms. The alkyl group of 2-8 carbon atoms represented by R
17 and R
18 in the general formula (5) may be linear or branched, including for example an ethyl
group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group,
nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl
group, pentadecyl group, hexadecyl group, heptadecyl group and octadecyl group; the
allyl group, the alkylallyl group or the allylalkyl group, having 6 to 18 carbon atoms
and being represented by R
17 and R
18, includes for example a phenyl group, benzyl group, phenetyl group, methylbenzyl
group, diphenylmethyl group and the like.
[0022] Olefin sulfide, fish oil sulfide and whale oil sulfide, to be blended with the lubricant
composition of the invention, should be olefin sulfide (polysulfide) being produced
by sulfide processing of polymers such as isobutylene and having a sulfur content
of 25 to 40% by weight, fish oil sulfide and whale oil sulfide produced by processing
individually fish oil and whale oil in the same manner.
[0023] European Patent Application EP 0725130A2 to the Tonen Corporation describes a lubricating
oil composition containing a majority of an oil of lubricating viscosity, a molybdenum
dithiocarbamate, an organozinc compound, and a phenol based antioxidant.
[0024] Thus, it is known in the art to use organomolybdenum compounds to reduce frictional
properties of lubricant oils and to use sulfur compounds as sulfur donors, as well
as phenolic antioxidants, to suppress oxidative degradation of the organomolybdenum
compounds.
SUMMARY OF THE INVENTION
[0025] In the instant invention, compositions and methods are provided for reducing copper
corrosion problems of lubricating oils containing organomolybdenum compounds together
with a sulfur containing compound. The sulfur containing compounds include those listed
above in WO 96/06904, diaryl sulfides, and sulfurized phenates as described in U.S.
Patent No. 5,328,620 which is herein incorporated by reference for disclosure of said
sulfurized phenates. The sulfurized phenates may be prepared from a phenol, elemental
sulfur and a metal. Also included in the definition of sulfur compounds are carbamates
as described in U.S. Patent No. 4,758,362 which is herein incorporated by reference
for said carbamate disclosure. Also included in the definition of sulfur containing
compounds are metal disulfides of formula M-S-S-M where M is a metal.
[0026] It is thought that the sulfur compounds act as peroxide destroyers and that such
peroxide destroyers degrade the molybdenum dithiocarbamates and thus shorten the useful
life span or the friction reducing oils containing them.
[0027] While the addition of sulfur compounds to oils reduces degradation of the organomolybdenum
compounds, said sulfur compounds cause increased copper corrosion properties of such
oils. The copper corrosion results from unbound or active sulfur contained with said
sulfur compounds.
[0028] We have discovered that in order to reduce copper corrosion properties of such oils,
the sulfur compounds must be treated with compounds to reduce the active or non-bound
sulfur of said sulfur compounds. Thus we have found that when copper corrosiveness
of sulfur compounds for use in additive packages containing molybdenum dithiocarbamates
and oxyo and sulfurized derivatives thereof are mixed with sunflower oil or other
plant oil and heated prior to adding to said additive package, the copper corrosiveness
of oils containing said additive packages is reduced. In theory the reduced copper
corrosiveness is reduced because the unbound or active sulfur associated with said
sulfur compounds is removed by reaction with the double bonds of the plant oils.
DETAILED DESCRIPTION OF THE INVENTION
[0029] The instant invention comprises an additive package for use in oils of lubricating
viscosity to provide said oils containing said packages with improved frictional and
reduced copper corrosion properties.
[0030] The additive package comprises a composition formed by mixing together:
A. a molybdenum dithiocarbamate;
B. a sulfur compound;
C. a plant oil;
wherein B. and C. are first mixed and heated together at time and temperature parameters
to react unbound or active sulfur of B. with C. prior to mixing with A.
[0031] The additive package described above when mixed with an oil of lubricating viscosity
provides for a lubricating composition having improved frictional properties and reduced
copper corrosion activity. The lubricating oil composition comprises a lubricating
composition formed by mixing:
A. a majority of an oil of lubricating viscosity;
B. a molybdenum dithiocarbamate;
C. a sulfur compound;
D. a plant oil;
wherein C and D are first mixed and heated together at time and temperature parameters
to react unbound or active sulfur of C. and D. prior to mixing with A. and B.
[0032] The instant invention also provides a method for reducing copper corrosion in internal
combustion engines. The method comprises adding to and operating said engine a lubricating
oil composition comprising a mixture formed by mixing:
A. a majority of an oil of lubricating viscosity;
B. a molybdenum dithiocarbamate;
C. a sulfur compound;
D. a plant oil.
[0033] The term "majority" is generally intended to mean that the lubricating oil compositions
contain a major amount of the oil of lubricating viscosity, that is the oil generally
comprises the constituent present in the largest amount in the composition and is
usually present in an amount more than 50% of the composition by weight.
[0034] The molybdenum dithiocarbamate for use in this invention includes those incorporated
by reference in the section above herein labeled "Background of the Invention".
[0035] The molybdenum dithiocarbamate compounds in addition to those described above include
those disclosed in WO 96/23856, WO 96/06904 and EP 0725130. In general the molybdenum
dithiocarbamates are alkyl and dialkyl dithiocarbamates and are available as Akeda
S-100 from Asaki Denka Kogyo K.K., Tokyo 103 Japan and as various MOLYVAN® compositions
from R.T. Vanderbilt Company of Norwalk, Connecticut, U.S.A..
[0036] Vanderbilt organomolybdenum dithiocarbamate compounds are MOLYVAN® A, a molybdenum
oxysulfide dithiocarbamate of the formula:

and MOLYVAN® 822 described by Vanderbilt as an organomolybdenum dithiocarbamate.
[0037] The sulfur compounds for use in the invention's compositions are those described
hereinabove. The sulfur compounds act as sulfur donors and contribute to copper corrosion
due to their unbound or active sulfur component. In preferred embodiments of the instant
invention the sulfur compounds are dibenzyl disulfide, sulfurized phenols and phenates
as described in U.S. Patents 5,328,620: 3,372,116 and 3,410,798 and dithiocarbamate
compounds described in U.S. Patent No. 4,758,362. Preferred sulfur compounds are sulfur
coupled dodecylphenol and its calcium overbased salt.
[0038] The plant oil with which the sulfur compound is mixed and heated for time and temperature
parameters to reduce unbound or active sulfur is preferably sunflower oil but other
plant oils with C=C unsaturation may also be used. The important requirement for the
oils is that they contain C=C unsaturation with which sulfur can react. The ratio
of sunflower oil (SFO) to sulfur compound depends on the activity of the sulfur in
the sulfur compound. Usually a weight ratio of 5 : 1 to 1 : 1 for the weight ratio
of SFO to sulfur compound is preferred but ratios of less than 1 : 1 and down to 0.5
: 1 by weight may also be used.
[0039] Prior to mixing with other components to form an additive package or containing said
additive package the SFO and sulfur compound are mixed and heated under parameters
by which the unbound or active sulfur of the sulfur compound reacts with unsaturated
sights in the SFO. A preferred range of reaction time and temperature is about 3 hours
at 90°C but other suitable parameters can easily be decided upon.
Examples
[0040] In the following examples, the percents given are weight percent on an oil free basis
for the weight of components based on the total weight of the oil composition except
for the Akeda S-100 molybdenum dithiocarbamate compound which is used as purchased.
Oil A
[0041] A majority of a Tonen base oil and added thereto:
1. 3.05 weight percent

n 2,000 ashless polyisobutylene/polyamine dispersant;
2. 0.36 weight percent zinc dithiophosphate di-2-ethylhexyl ester;
3. 0.58 weight percent zinc dithiophosphate isopropyl, methylamyl ester;
4. 1.34 weight percent calcium overbased sulfur coupled dodecyl phenol;
5. 1.2 weight percent Akeda S-100 molybdenum dithiocarbamate;
6. 4.0 weight percent C12-isopropyl, diisobutylphenol.
Oil B
[0042]
1. Oil A plus
2. 0.29 weight percent sulfur coupled dodecylphenol.
Oil C
[0043]
1. OilA
2. 0.58 weight percent sulfur coupled dodecylphenol
Oil D
[0044]
1. Oil A
2. 1.0 weight percent sunflower oil
Oil E
[0045]
1. Oil C
2. 1.0 weight percent sunflower oil
Oil F
[0046]
1. Oil A
2. 0.2 weight percent dibutyldisulfide
Oil G
[0047]
1. Oil F
2. 1.0 weight percent sunflower oil
[0048] In general, the range of weight percents of components in the total oil composition
range from 1-10 weight percent polyisobutylene/polyamine dispersant and/or its borated
derivative; 0.1-5 weight percent of a dihydrocarbon dithiophosphate where hydrocarbon
is given an expansive reading; 0.1-7 weight percent of a sulfur coupled alkyl phenol
and/or its calcium overbased salt, 0.1-5 weight percent of a molybdenum dithiocarbamate
and 0.1-10 weight percent of an antioxidant.
[0049] For the oils above (A-G) copper strips were soaked in oil at 120°C for 192 hours.
An arbitrary rating of 1A - 4A was ascribed to copper corrosion on the individual
strips. 1A was judged to be the least corroded (least-darkened) and 4A the most corroded
(most-darkened) value prescribed to the strips. Table 1 below shows the results.
Table 1
Oil |
A |
B |
C |
D |
E |
F |
G |
Corrosion |
2A |
3A |
3A |
1A |
1A |
4A |
1A |
[0050] The results above clearly show that the addition of a sulfur donor causes copper
corrosion when added to a molybdenum dithiocarbamate containing oil (Oils B, C, F)
but the corrosion is negated when the sulfur donor is first heated with sunflower
oil as described hereinabove and the SFO/sulfur compound then added to the oil additive
mixture which is then added to the oil (Oils D, E, G).
[0051] Copper strips used in the copper corrosion test for Oils C and E were examined in
detail for the effects of copper corrosion and the chemical elements associated with
said corrosion. In this a cross section of the copper plates used with Oils C and
E were polished and examined microscopically. Microscopic photographs of cross sections
from copper plates are shown in FIGURES 1 and 2 for plates corroded respectively with
Oil C and Oil E. The photos demonstrated conclusively that the corrosion caused by
sulfur coupled dodecylphenol in Oil C is largely eliminated by first heating said
phenol with SFO prior to adding to Oil E.
[0052] The copper plates used in the copper corrosion test in Oils C and E herein described
above were further subjected to EPMA analysis. Photos revealed that the copper plate
from Oil E was not corroded while that tested in Oil C was heavily corroded. A line
analysis using EPMA was then conducted on the copper plate tested in Oil C. The results
of the EPMA line analysis are shown in FIGURE 3. FIGURE 3 shows that at a given area
of corrosion on the corroded copper plate that the copper content is greatly diminished
compared to a non-corroded area. The Figure demonstrates that in areas of diminished
copper content (corroded areas) the concentration of phosphorus, zinc and sulfur are
very high. This result demonstrates the corrosive effects of zinc and phosphorus as
well as sulfur. For a qualitative description of EPMA (Election Probe Microanalysis)
see http://darkening.uoregon.edu/-mshaf/epmahome/index.html which is incorporated
herein by reference.