BACKGROUND OF THE INVENTION
[0001] The present invention relates to a grease composition for a constant velocity joint,
namely a fixed type joint and a slide type joint.
[0002] Generally, in FF type or front engine-front wheel driven type cars, a constant velocity
joint is employed in a combination of a fixed type joint, a shaft, and a thrust type
joint.
[0003] The fixed type joint includes a Birfield joint, a Rzeppa joint, an undercutting free
joint, a tripod joint, and the like. The slide type joint includes a double off-set
joint, a tripod joint, a closs groove joint, and the like.
[0004] As a conventional lubricant charged into such constant velocity joints, an extreme
pressure grease is mainly employed in which a base grease consisting of a purified
mineral oil and a lithium soap and/or urea thickener is combined with molybdenum disulfide,
a lead compound, or the like.
[0005] It is required for the grease composition for a constant velocity joint to exhibit
performances such as anti- flaking, anti-seizure, abrasion resistance, low friction,
or the like. However, the performance of the conventional grease hardly catch up with
the tendency to improved performance and quality of cars. Thus, particularly in order
to prolong the life time of a constant velocity joint, improvement in the anti-flaking
property is desired.
SUMMARY OF THE INVENTION
[0006] It is therefore an object of the present invention to provide a grease composition
for a constant velocity joint which exhibits superior anti-flaking performance and
which can prolong the life time of a constant velocity joint.
[0007] According to the present invention, there is provided a grease composition for a
constant velocity joint comprising a base oil, a thickener, boron nitride powders,
and a sulfur- phosphorus containing extreme pressure agent, said thickener being contained
in an amount of 2 to 25 weight %, said boron nit ride powders being contained in an
amount of 0.5 to 20 weight %, and said sulfur-phosphorus containing extreme pressure
agent being contained in an amount of 0.1 to 10 weight %, each based on a total weight
of said grease composition.
PREFERRED EMBODIMENTS OF THE INVENTION
[0008] The present invention will be explained in more detail hereinbelow.
[0009] The base oil contained in the grease composition for a constant velocity joint of
the present invention may preferably be a mineral oil and/or a synthetic oil. The
mineral oil may be obtained by a conventional method commonly performed in a lube
oil production process in oil refining industries. For example, a base oil obtained
by distilling a crude oil under atmospheric or reduced pressure to obtain lubricant
fractions, and refining the lubricant fractions by at least one treatment selected
from solvent deasphalting, solvent extraction, hydrocracking, solvent dewaxing, contact
dewaxing, hydrofining, washing with sulfuric acid, clay treatment, and the like, may
be used.
[0010] Examples of the synthetic oil may include poly-α-olefins such as polybutene, 1-octen
oligomer, and 1-decene oligomer, or hydrides of these poly-α-olefins; diesters such
as ditridecyl glutarate, di-2-ethylhexyl adipate, diisodecyl adipate, ditridecyl adipate,
or di-3-ethylhexyl sebacate; polyol esters such as trimethylolpropane caprylate, trimethylolpropane
pelargonate, pentaerythritol-2-ethyl hexanoate, or pentaerythritol pelargonate; alkylnaphthalene;
alkylbenzene; polyoxyalkylene glycol; polyphenyl ether; dialkyldiphenylether, silicone
oil; or perfluoroalkyl ether. These may be used alone or in mixture.
[0011] The viscosity range of the base oil may be any of commonly used lube oils, but usually
kinematic viscosity at 100 °C of 2 to 40 mm
2/s, preferably 3 to 20 mm
2/s is desirable. Further, the viscosity index of the base oil is preferably not less
than 90, more preferably not less than 100.
[0012] The grease composition for a constant velocity joint of the present invention contains
as a requisite component a thickener. The thickener may be selected from a variety
of thickeners, for example, soap thickeners such as a metal soap, and a complex metal
soap; and non-soap thickeners such as bentone, silica gel, urea compounds, urea-urethane
compounds, and urethane compounds. Among these, urea compounds, urea-urethane compounds,
urethane compounds, and mixtures thereof are particularly preferred in view of their
heat resistance.
[0013] Examples of the soap thickener may include, for example, sodium soap, calcium soap,
aluminum soap, or lithium soap.
[0014] Examples of the urea compounds, urea-urethane compounds, and urethane compounds may
include, for example, diurea compounds, trirurea compounds, tetraurea compounds, other
polyurea compounds, urea-urethane compounds, diurethane compounds, and mixtures thereof.
Among these, diurea compounds, urea-urethane compounds, diurethane compounds, and
mixtures thereof are particularly preferred. Specifically, a compound or a mixture
of compounds represented by the formula (1) is preferred:
A-CONH-R
1-NHCO-B (1)
wherein R
1 stands for a divalent hydrocarbon group, A and B may be the same or different groups
and each stands for -NHR
2, -NR
3R
4, or -OR
5, wherein R
2, R
3, R
4, and R
5 are the same or different groups and each stands for a hydrocarbon residue having
6 to 20 carbon atoms.
[0015] In the above formula (1), R
1 stands for a divalent hydrocarbon group having preferably 6 to 20, more preferably
6 to 15 carbon atoms. Examples of the divalent hydrocarbon group may include a straight
chain or branched alkylene group, a straight chain or branched alkenylene group, a
cycloalkylene group, or an aromatic group. Specific examples of R
1 may include ethylene group, 2,2-dimethyl-4-methylhexylene group, and groups represented
by the formulae (a) to (j) below:

Among these, (d) and (e) are particularly preferred.
[0016] In the above formula (1), R
2, R
3, R
4, and R
5 may stand for a straight chain or branched alkyl group, a straight chain or branched
alkenyl group, a cycloalkyl group, an alkylcycloalkyl group, an aryl group, an alkylaryl
group, or an arylalkyl group. Specifically, for example, they may stand for a straight
chain or branched alkyl group such as hexyl group, heptyl group, octyl group, nonyl
group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group,
pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group,
or eicocyl group; a straight chain or branched alkenyl group such as hexenyl group,
heptenyl group, octenyl group, nonenyl group, decenyl group, undecenyl group, dodecenyl
group, tridecenyl group, tetradecenyl group, pentadecenyl group, hexadecenyl group,
heptadecenyl group, octadecenyl group, nonadecenyl group, or eicocenyl group; cyclohexyl
group; an alkylcycloalkyl group such as methylcyclohexyl group, dimethylcyclohexyl
group, ethylcyclohexyl group, diethylcyclohexyl group, propylcyclohexyl group, isopropylcyclohexyl
group, 1-methyl-3-propylcyclohexyl group, butylcyclohexyl group, amylcyclohexyl group,
amylmethylcyclohexyl group, hexylcyclohexyl group, heptylcyclohexyl group, octylcylcohexyl
group, nonylcyclohexyl group, decylcyclohexyl group, undecylcyclohexyl group, dodecylcyclohexyl
group, tridecylcyclohexyl group or tetradecylcyclohexyl group; an aryl group such
as phenyl group or naphthyl group; an alkylaryl group such as toluyl group, ethylphenyl
group, xylyl group, propylphenyl group, cumenyl group, methylnaphthyl group, ethylnaphthyl
group, dimethylnaphthyl group or propylnaphthyl group; or an arylalkyl group such
as benzyl group, methylbenzyl group or ethylbenzyl group. Among these, cyclohexyl
group, octadecyl group, and toluyl group are particularly preferred.
[0017] The diurea compound, the urea-urethane compound, or the diurethane compound may be
prepared by reacting diisocyanate represented by the formula OCN-R
1-NCO with a compound represented by the formula R
2NH
2, R
3R
4NH, or R
5OH or mixtures thereof in the base oil at 10 to 200 °C. In this case, R
1, R
2, R
3, R
4 , and R
6 are the same as those in the formula (1).
[0018] The content of the thickener is 2 to 25 weight %, preferably 3 to 20 weight % of
the total weight of the grease composition. If the content of the thickener is less
than 2 weight %, the effect of the thickener is not enough so that the composition
cannot be in a sufficiently greasy state. If the content of the thickener is more
than 25 weight %, the composition becomes too hard for grease so that the composition
cannot exhibit sufficient lubricating performance.
[0019] The grease composition of the present invention contains as a requisite component
boron nitride powders. The particle size of the boron nitride powders is not particularly
limited, but the average particle size thereof is usually 0.05 to 20 µm, preferably
0.4 to 15 µm, more preferably 5 to 10 µm.
[0020] The content of the boron nitride powders is 0.5 to 20 weight %, preferably 1 to 20
weight % of the total weight of the grease composition. If the content of the boron
nitride powders is less than 0.5 weight %, enough anti-flaking performance cannot
be exhibited, and the anti-seizure performance of a constant velocity joint becomes
insufficient. If the content of the boron nitride powders is more than 20 weight %,
abrasion (wear due to abrasive effect of powder particles) is promoted, and the life
time of a constant velocity joint becomes insufficient.
[0021] The grease composition of the present invention contains as a requisite component
a sulfur-phosphorus containing extreme pressure agent. The sulfur-phosphorus containing
extreme pressure agent may not only be a single extreme pressure agent containing
both sulfur and phosphorus, but also be a combination of a sulfur containing extreme
pressure agent containing only sulfur and a phosphorus containing extreme pressure
agent containing only phosphorus, provided that the sulfur-phosphorus containing extreme
pressure agent does not contain metal dithiophosphates such as molybdenum dithiophosphate
or zinc dithiophosphate.
[0022] The ratio of the sulfur atoms to the phosphorus atoms in the sulfur-phosphorus containing
extreme pressure agent is preferably in the range between 100 : 25 and 100 : 1.
[0023] Examples of the sulfur containing extreme pressure agent may include sulfurized oils
and fats, metal fenates cross-linked with sulfur, dihydrocarbyl polysulfide, dithiocarbamates,
monosulfide, sulfoxide, sulfinate, or mixtures thereof. Among these, sulfurized oils
and fats, dihydrocarbyl polysulfide, and mixtures thereof are particularly preferred.
[0024] The sulfurized oils and fats are compounds obtained by adding sulfur to animal or
vegetable oils and fats having unsaturated bond such as olive oil, caster oil, tea
seed oil, rice bran oil, cotton seed oil, rape seed oil, corn oil, beef tallow, neatsfoot
oil, sperm oil, or whale paraffin, followed by heating the mixture. The content of
sulfur in the sulfurized oils and fats is usually 5 to 15 weight %, preferably 8 to
12 weight %.
[0025] Examples of the metal fenate cross-linked with sulfur may include alkaline earth
metal salts of sulfides of alkylphenol to which an alkyl group(s) having 8 to 30,
preferably 9 to 20 carbon atoms is added. Specific examples of the alkyl group may
include octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl
group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl
group, nonadecyl group, icosyl group, henicosyl group, docosyl group, tricosyl group,
tetracosyl group, pentacosyl group, hexacosyl group, heptacosyl group, octacosyl group,
nonacosyl group, or triacontyl group, and these groups may either be straight chain
or branched. Among these, an alkyl group derived from nonene, or olefins or alcohols
having 5 to 8 carbon atoms is particularly preferred. The alkaline earth metal may
preferably be magnesium, calcium, or barium.
[0026] The dihydrocarbyl polysulfide is a compound represented by the formula (2):

wherein R
6 and R
7 may be the same or different groups and each may preferably stand for an alkyl group
having 3 to 18, preferably 6 to 15 carbon atoms derived from propylene or isobutene,
or an aryl group, an alkylaryl group, or an arylalkyl group, each having 6 to 8 carbon
atoms. Examples of these groups may include, for example, alkyl groups such as isopropyl
group, branched hexyl group derived from propylene dimer, branched nonyl group derived
from propylene trimer, branched dodecyl group derived from propylene tetramer, branched
pentadecyl group derived from propylene pentamer, branched octadecyl group derived
from propylene hexamer, tert-butyl group, branched octyl group derived from isobutene
dimer, branched dodecyl group derived from isobutene trimer, or branched hexadecyl
group derived from isobutene tetramer (these alkyl groups include all of branch isomers)
; alkylaryl groups such as phenyl group, tolyl group, ethylphenyl group, or xylyl
group (an alkyl group portion of these alkylaryl groups may be straight chain or branched,
and substituting position of an alkyl group portion on an aryl group is arbitrary);
or arylalkyl groups such as benzyl group, or phenylethyl group (substituting position
of a phenyl group is arbitrary).
[0027] z in the formula (2) above stands for an integer of 1 to 5, preferably 2 to 4. When
z is 3 or larger, the sulfur atoms may form a circle, for example,

[0028] Specific examples of the dihydrocarbyl polysulfide may include dibutyl polysulfide,
dihexyl polysulfide, dioctyl polysulfide, dinonyl polysulfide, didecyl polysulfide,
didodecyl polysulfide, ditetradecyl polysulfide, dihexadecyl polysulfide, dioctadecyl
polysulfide, dieicosyl polysulfide, diphenyl polysulfide, dibenzyl polysulfide, diphenethyl
polysulfide, polypropenyl polysulfide, polybutenyl polysulfide, or mixtures thereof.
Among these, polypropenyl polysulfide, polybutenyl polysulfide, and mixtures thereof
are particularly preferred.
[0029] The polypropenyl polysulfide, polybutenyl polysulfide, or mixtures thereof may be
obtained by sulfurizing an olefin hydrocarbon such as propylene, isobutene, dimer,
trimer, or tetramer of these monomers, or mixtures of these monomers and/or polymers
thereof with sulfur, sulfur halide (e.g. sulfur monochloride or sulfur dichloride),
sulfurized hydrogen, or mixtures thereof.
[0030] The content of sulfur in the dihydrocarbyl polysulfide is usually 30 to 50 weight
%, preferably 40 to 45 weight %.
[0031] The dithiocarbamate may be an alkyldithiocarbamyl compound represented by the formula
(3):

wherein R
8, R
9, R
10, and R
11 are the same or different groups and each stands for a straight chain or branched
alkyl group having 1 to 18, preferably 1 to 10 carbon atoms, for example, an alkyl
group such as methyl group, ethyl group, propyl group, n-butyl group, isobutyl group,
pentyl group, isopentyl group, hexyl group, heptyl group, octyl group, 2-ethylhexyl
group, nonyl group, decyl group, tridecyl group, or octadecyl group.
[0032] In the formula (3), (Y) stands for S, S-S, S-CH
2-S, S-(CH
2)
2-S, S-(CH
2)
3-S, or S-Zn-S.
[0033] Specific examples of the alkyldithiocarbamyl compound may include methylene bis (dibutyldithiocarbamate),
bis (dimethylthiocarbamyl) monosulfide, bis(dimethylthiocarbamyl) disulfide, bis(dibutylthiocarbamyl)
disulfide, bis (dipentylthiocarbamyl) disulfide, bis (dioctylthiocarbamyl) disulfide,
or zinc dipentyldithiocarbamate.
[0034] The phosphorus containing extreme pressure agent may be a phosphate, a phosphite,
a phosphinate, a phosphonate, or an amine salt thereof, or mixtures thereof. Among
these, phosphates, phosphites, and mixtures thereof are particularly preferred.
[0035] The phosphate herein is a compound represented by the formula (4), and the phosphite
herein is a compound represented by the formula (5):

wherein R
12 stands for an alkyl group, a cycloalkyl group, an alkylcycloalkyl group, an alkenyl
group, an aryl group, an alkylaryl group, or an arylalkyl group, each having 1 to
24 carbon atoms, R
13 and R
14 each stands for a hydrogen atom, an alkyl group, a cycloalkyl group, an alkylcycloalkyl
group, an alkenyl group, an aryl group, an alkylaryl group, or an arylalkyl group,
each having 1 to 24 carbon atoms.
[0036] Specific examples of R
13, R
13, and R
14 other than hydrogen atom may include methyl group, ethyl group, propyl group, butyl
group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group,
dodecyl group, tetradecyl group, hexadecyl group, octadecyl group, eicosyl group,
docosyl group, tetracosyl group, cyclopentyl group, cyclohexyl group, methylcyclohexyl
group, ethylcyclohexyl group, dimethylcyclohexyl group, cycloheptyl group, phenyl
group, tolyl group, xylyl group, ethylphenyl group, propylphenyl group, butylphenyl
group, pentylphenyl group, hexylphenyl group, nonylphenyl group, decylphenyl group,
dodecylphenyl group, tetradecylphenyl group, hexadecylphenyl group, octadecylphenyl
group, benzyl group, or phenethyl group.
[0037] Specific examples of the phosphorus containing extreme pressure agent may include
tributyl phosphate, benzyl diphenyl phosphate, ethyl diphenyl phosphate, octyl diphenyl
phosphate, triphenyl phosphate, tricresylphosphate, tritolyl phosphate, 2-ethylhexyl
diphenyl phosphate, tributyl phosphite, or dilauryl phosphite.
[0038] Particularly preferred combination of the sulfur containing extreme pressure agent
and the phosphorus containing extreme pressure agent may be a combination of the dihydrocarbyl
polysulfide and the phosphate, or a combination of the sulfurized oils and fats and
the phosphate.
[0039] The single extreme pressure agent containing both sulfur and phosphorus may be a
thiophosphate, a thiophosphite, or mixtures thereof. The thiophosphate and the thiophosphite
may be compounds represented by the formulae (4) and (5) of the phosphate and phosphite
wherein at least one oxygen atom is substituted by a sulfur atom.
[0040] The content of the sulfur-phosphorus containing extreme pressure agent in the grease
composition of the present invention is 0.1 to 10 weight %, preferably 1 to 5 weight
% of the total weight of the grease composition. If the content of the sulfur-phosphorus
containing extreme pressure agent is less than 0.1 weight %, the anti- seizure performance
of a constant velocity joint is not sufficient. Even if the content of the sulfur-phosphorus
containing extreme pressure agent is more than 10 weight %, the increase in the content
will not meet the improvement in the performance of grease composition, thus being
not economical.
[0041] The grease composition for a constant velocity joint of the present invention may
optionally contain molybdenum dithiocarbamate as an extreme pressure agent in addition
to the sulfur-phosphorus containing extreme pressure agent. Specifically, the molybdenum
dithiocarbamate represented by the formula (6) may be employed:

wherein R
15, R
16, R
17, and R
18 are the same or different groups and each stands for a hydrocarbon group such as
alkyl group, alkenyl group, aryl group, alkylaryl group, or arylalkyl group, among
which an alkyl group is particularly preferred.
[0042] Specific examples of R
15, R
16, R
17, and R
18 may include straight chain or branched alkyl groups having 2 to 18, preferably 8
to 13 carbon atoms such as 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, or octadecyl group; alkylaryl groups such as butylphenyl group or nonylphenyl
group. Further X
1, X
2, X
3 , and X
4 each stands for a sulfur atom or an oxygen atom.
[0043] Specific examples of the molybdenum dithiocarbamate may include molybdenum sulfide
diethyl dithiocarbamate, molybdenum sulfide dipropyl dithiocarbamate, molybdenum sulfide
dibutyl dithiocarbamate, molybdenum sulfide dipentyl dithiocarbamate, molybdenum sulfide
dihexyl dithiocarbamate, molybdenum sulfide dioctyl dithiocarbamate, molybdenum sulfide
didecyl dithiocarbamate, molybdenum sulfide didodecyl dithiocarbamate, molybdenum
sulfide ditridecyl dithiocarbamate, molybdenum sulfide di(butylphenyl) dithiocarbamate,
molybdenum sulfide di(nonylphenyl) dithiocarbamate, molybdenum oxysulfide diethyl
dithiocarbamate, molybdenum oxysulfide dipropyl dithiocarbamate, molybdenum oxysulfide
dibutyl dithiocarbamate, molybdenum oxysulfide dipentyl dithiocarbamate, molybdenum
oxysulfide dihexyl dithiocarbamate, molybdenum oxysulfide dioctyl dithiocarbamate,
molybdenum oxysulfide didecyl dithiocarbamate, molybdenum oxysulfide didodecyl dithiocarbamate,
molybdenum oxysulfide ditridecyl dithiocarbamate, molybdenum oxysulfide di(butylphenyl)
dithiocarbamate, or molybdenum oxysulfide di(nonylphenyl)dithiocarbamate. These compounds
may be used alone or in mixture.
[0044] The content of the molybdenum dithiocarbamate, if contained, in the grease composition
of the present invention is usually 0.1 to 10 weight %, preferably 1 to 5 weight %
of the total weight of the grease composition.
[0045] When both the molybdenum dithiocarbamate and the sulfur-phosphorus containing extreme
pressure agent are employed in combination, the ratio of the molybdenum dithiocarbamate
to the sulfur-phosphorus containing extreme pressure agent is usually 1 : 5 to 5 :
1, preferably 1 : 3 to 3 : 1 by weight.
[0046] The grease composition of the present invention may additionally be admixed with
an organozinc compound for further improving the anti-flaking performance. Examples
of the organozinc compound may include, for example, zinc dithiophosphate, zinc dithiocarbamate,
zinc salts of fatty acids, or zinc naphthenate.
[0047] The zinc dithiophosphate may be a compound represented by the formula (7):

wherein R
19 , R
20, R
21, and R
22 are the same or different groups and each stands for a straight chain or branched
primary or secondary alkyl group, aryl group, or arylalkyl group, each having 2 to
18 carbon atoms, such as 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, or octadecyl group.
[0048] The zinc dithiocarbamate may be a compound represented by the formula (8):

wherein R
23, R
24, R
26, and R
26 are the same or different groups and each stands for an alkyl group, an alkenyl group,
an aryl group, an alkylaryl group, or an arylalkyl group, each having 2 to 18 carbon
atoms, specifically, an alkyl group such as 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, or octadecyl group (these alkyl groups may be straight chain
or branched, and may be primary or secondary); or an alkylaryl group such as butylphenyl
group or nonylphenyl group (an alkyl portion of these alkylaryl groups may be straight
chain or branched, and a substituting position of an alkyl portion on the aryl group
is arbitrary).
[0049] The zinc salt of a fatty acid may be a compound represented by the formula (9) (R
27COO)
2Zn (9), wherein R
27 stands for an alkyl group or an alkenyl group, each having 3 to 22 carbon atoms.
[0050] The zinc naphthenate may be a compound represented by the formula (10)

wherein R
28 stands for a cycloalkyl group such as cyclopentyl group, cyclohexyl group, alkylcyclopentyl
group, or alkylcyclohexyl group, and m stands for an integer.
[0051] The content of the organozinc compound, if contained, in the grease composition of
the present invention is usually 0.1 to 10 weight %, preferably 1 to 5 weight % of
the total weight of the grease composition.
[0052] Further, the grease composition for a constant velocity joint of the present invention
may be admixed with additional additives such as a solid lubricant, an extreme pressure
agent other than the sulfur-phosphorus containing extreme pressure agent and the molybdenum
dithiocarbamate, an anti-oxidant, an oilness agent, a rust-inhibitor, or a viscosity
index improver, if required, for further improving the performance of the grease composition,
as long as the additional additives do not damage the properties of the grease composition.
[0053] Examples of the solid lubricant may include, for example, carbon black, fluorinated
carbon black, polytetrafluoroethylene, molybdenum disulfide, antimony sulfide, or
an alkali or an alkaline earth metal borate.
[0054] Examples of the extreme pressure agent other than the sulfur-phosphorus containing
extreme pressure agent and the molybdenum dithiocarbamate may include chlorine compounds
such as chlorinated paraffin or a chlorinated ester; or molybdenum compounds such
as molybdenum dithiophosphate.
[0055] Examples of the anti-oxidant may include phenol compounds such as 2,6-di-t-butylphenol,
or 2,6-di-t-butyl-p-cresol; amine compounds such as dialkyldiphenyl amine, phenyl-α-naphthyl
amine, or p-alkylphenyl-α-naphthyl amine; sulfur compounds; or phenothiazine compounds.
[0056] Examples of the oilness agent may include amines such as lauryl amine, myristyl amine,
palmityl amine, stearyl amine, or oleyl amine; higher alcohols such as lauryl alcohol,
myristyl alcohol, palmityl alcohol, stearyl alcohol, or oleyl alcohol; higher fatty
acids such as lauric acid, myristic acid, palmitic acid, stearic acid, or oleylic
acid; fatty acid esters such as methyl laurate, methyl myristate, methyl palmitate,
methyl stearate, or methyl oleate; amidos such as lauryl amido, myristyl amido, palmityl
amido, stearyl amido, or oleyl amido; or fats and oils.
[0057] Examples of the rust-inhibitor may include metal soaps; synthetic sulfonates such
as petroleum sulfonate, alkylbenzene sulfonate, or dinonylnaphthalene sulfonate; partial
esters of polyalcohol such as sorbitan fatty acid ester; amines; phosphoric acid;
or phosphates.
[0058] Examples of the viscosity index improver may include polymethacrylate, polyisobutylene,
or polystyrene.
[0059] The grease composition for a constant velocity joint of the present invention may
be prepared, for example, by adding the thickener, the boron nit ride powders, the
sulfur-phosphorus containing extreme pressure agent, and optionally the molybdenum
dithiocarbamate, the organozinc compound, or other additives mentioned above, to the
base oil, agitating the resulting mixture, and passing the mixture through a roll
mill. Alternatively, raw material components of the thickener may preliminarily be
added to the base oil, dissolved and mixed together by stirring, so that the thickener
may be prepared simultaneously with the preparation of the grease composition of the
present invention.
[0060] The grease composition for a constant velocity joint of the present invention is
superior in the antiflaking performance, and can prolong the life time of a constant
velocity joint.
EXAMPLES
[0061] The present invention will be explained in more detail with reference to Examples
and Comparative Examples. However, the present invention is not limited thereto.
Example 1
[0062] 88.0 g of diphenylmethane-4,4'-diisocyanate were added to 350 g of mineral oil, and
the mixture was heated to 60 °C to obtain a homogeneous solution. Then another solution
obtained by dissolving 26.2 g of dodecylalcohol in 200 g of the same mineral oil by
heating was added to the former solution, and the mixture was agitated vigorously.
To the mixture, another solution obtained by dissolving 55.8 g of cyclohexylamine
in 205 g of the same mineral oil was added, and the resulting mixture was again agitated
vigorously to obtain a gel. The gel was kept at 100 °C for 30 minutes under agitation,
admixed with additives containing a thickener, boron nitride powders, and an extreme
pressure agent. The obtained mixture was agitated and passed through a three-roll
roll mill, thereby preparing a grease composition. The obtained grease composition
was evaluated by the following method. The result is shown in Table 1. The composition
of the grease composition is shown below.
Composition
[0063]
Thickener |
17.0 weight % |
Mineral oil (126 mm2 /s @40°C) |
77.5 weight % |
Boron nitride powders (average particle size: 0.7 µm) |
1.5 weight % |
Sulfurized oils and fats (sulfur content: 9 to 10 weight %) |
2.0 weight % |
Tributylphosphite |
1.0 weight % |
Amine anti-oxidant (mixture consistency: 283) |
1.0 weight % |
[0064] The thickener employed in this Example is a mixture of the following compounds:

wherein A stands for an N-cyclohexylamino group, B stands for a dodecyloxy group,
and the ratio of A to B in the mixture is 80 : 20.
On-Bench Durability Test
[0065] Using a commercially available Birfield joint of #87 size, the life time of the joint
was evaluated under the condition of the predetermined high speed rotation and high
torque.
Comparative Example 1
[0066] A grease composition having similar composition to that of Example 1 was prepared
in the same way as in Example 1 except that the sulfurized oils and fats and tributylphosphite
were not added but replaced by the mineral oil of the equivalent weight. The obtained
grease composition was evaluated in the same way as in Example 1. The result is shown
in Table 1. The composition of the grease composition is shown below.
Composition
[0067]
Thickener (same as that of Example 1) |
17.0 weight % |
Mineral oil (126 mm2/s @40°C) |
80.5 weight % |
Boron nitride powders (average particle size: 0.7 µm) |
1.5 weight % |
Amine anti-oxidant (mixture consistency: 298) |
1.0 weight % |
Comparative Example 2
[0068] A grease composition having similar composition to that of Example 1 was prepared
in the same way as in Example 1 except that boron nitride powders were not added by
replaced by the mineral oil of the equivalent weight. The obtained grease composition
was evaluated in the same way as in Example 1. The result is shown in Table 1. The
composition of the grease composition is shown below.
Composition
[0069]
Thickener (same as that in Example 1) |
17.0 weight % |
Mineral oil (126 mm2/s @40°C) |
79.0 weight % |
Sulfurized oils and fats (sulfur content: 9 to 10 weight %) |
2.0 weight % |
Tributylphosphite |
1.0 weight % |
Amine anti-oxidant (mixture consistency: 307) |
1.0 weight % |
Comparative Example 3
[0070] A grease composition having similar composition to that of Example 1 was prepared
in the same way as in Example 1 except that tributylphosphite was not added but replaced
by the mineral oil of the equivalent weight. The obtained grease composition was evaluated
in the same way as in Example 1. The result is shown in Table 1. The composition of
the grease composition is shown below.
Composition
[0071]
Thickener (same as that of Example 1) |
17.0 weight % |
Mineral oil (126 mm2/s @40°C) |
78.5 weight % |
Boron nitride powders (average particle size: 0.7 µm) |
1.5 weight % |
Sulfurized oils and fats (sulfur content: 9 to 10 weight %) |
2.0 weight % |
Amine anti-oxidant (mixture consistency: 289) |
1.0 weight % |
Comparative Example 4
[0072] A grease composition having similar composition to that of Example 1 was prepared
in the same way as in Example 1 except that the sulfurized oils and fats were not
added but replaced by the mineral oil of the equivalent weight. The obtained grease
composition was evaluated in the same way as in Example 1. The result is shown in
Table 1. The composition of the grease composition is shown below.
Composition
[0073]
Thickener (same as that of Example 1) |
17.0 weight % |
Mineral oil (126 mm2 /s @40°C) |
79.5 weight % |
Boron nitride powders (average particle size: 0.7 µm) |
1.5 weight % |
Tributyl phosphite |
1.0 weight % |
Amine anti-oxidant (mixture consistency: 304) |
1.0 weight % |
Example 2
[0074] 75 g of lithium-12-hydroxystearate were added to 550 g of mineral oil, and the former
was dissolved in the latter by heating to 200 °C under agitation. To the resulting
mixture, 320 g of the mineral oil was added, and rapidly cooled to obtain a gel. The
gel was kept at 100 °C for 30 minutes under agitation, and admixed with the additives.
The obtained mixture was passed through a three-roll roll mill, thereby preparing
a grease composition. The obtained grease composition was evaluated by the same way
as in Example 1. The result is shown in Table 1. The composition of the grease composition
is shown below.
Composition
[0075]
Lithium-12-hydroxystearate |
7.5 weight % |
Mineral oil (126 mm2 /s @40°C) |
87.0 weight % |
Boron nitride powders (average particle size: 0.7 µm) |
1.5 weight % |
Sulfurized oils and fats (sulfur content: 9 to 10 weight %) |
2.0 weight % |
Tricresyl phosphate |
1.0 weight % |
Amine anti-oxidant (mixture consistency: 288) |
1.0 weight % |
Example 3
[0076] A grease composition having similar composition to that of Example 2 was prepared
in the same way as in Example 2 except that tricresyl phosphate was replaced by tributylphosphite
of the equivalent weight. The obtained grease composition was evaluated in the same
way as in Example 1. The result is shown in Table 1. The composition of the grease
composition is shown below.
Composition
[0077]
Lithium-12-hydroxystearate |
7.5 weight % |
Mineral oil (126 mm2 /s @40°C) |
87.0 weight % |
Boron nitride powders (average particle size: 0.7 µm) |
1.5 weight % |
Sulfurized oils and fats (sulfur content: 9 to 10 weight %) |
2.0 weight % |
Tributylphosphite |
1.0 weight % |
Amine anti-oxidant (mixture consistency: 286) |
1.0 weight % |
Example 4
[0078] A grease composition having similar composition to that of Example 2 was prepared
in the same way as in Example 2 except that the sulfurized oils and fats were replaced
by polysulfide of the equivalent weight. The obtained grease composition was evaluated
in the same way as in Example 1. The result is shown in Table 1. The composition of
the grease composition is shown below.
Composition
[0079]
Lithium-12-hydroxystearate |
7.5 weight % |
Mineral oil (126 mm2/s @40°C) |
87.0 weight % |
Boron nitride powders (average particle size: 3 µm) |
1.5 weight % |
Dihydrocarbyl polysulfide (sulfur content: 42 weight %) |
2.0 weight % |
Tricresyl phosphate |
1.0 weight % |
Amine anti-oxidant (mixture consistency: 285) |
1.0 weight % |
Example 5
[0080] A grease composition having similar composition to that of Example 2 was prepared
in the same way as in Example 2 except that tricresyl phosphate was replaced by tributylphosphite
of the equivalent weight and the sulfurized oils and fats were replaced by polysulfide
of the equivalent weight. The obtained grease composition was evaluated in the same
way as in Example 1. The result is shown in Table 1. The composition of the grease
composition is shown below.
Composition
[0081]
Lithium-12-hydroxystearate |
7.5 weight % |
Mineral oil (126 mm2/s @40°C) |
87.0 weight % |
Boron nitride powders (average particle size: 0.7 µm) |
1.5 weight % |
Dihydrocarbyl polysulfide (sulfur content: 42 weight %) |
2.0 weight % |
Tributyl phosphite |
1.0 weight % |
Amine anti-oxidant (mixture consistency: 287) |
1.0 weight % |
Comparative Example 5
[0082] A grease composition having similar composition to that of Example 2 was prepared
in the same way as in Example 2 except that the sulfurized oils and fats and tricresyl
phosphate were not added but replaced by the mineral oil of the equivalent weight.
The obtained grease composition was evaluated in the same way as in Example 1. The
result is shown in Table 1. The composition of the grease composition is shown below.
Composition
[0083]
Lithium-12-hydroxystearate |
7.5 weight % |
Mineral oil (126 mm2/s @40°C) |
90.0 weight % |
Boron nitride powders (average particle size: 3 µm) |
1.5 weight % |
Amine anti-oxidant (mixture consistency: 298) |
1.0 weight % |
Comparative Example 6
[0084] A grease composition having similar composition to that of Example 5 was prepared
in the same way as in Example 2 except that the boron nit ride powders were not added
but replaced by the mineral oil of the equivalent weight. The obtained grease composition
was evaluated in the same way as in Example 1. The result is shown in Table 1. The
composition of the grease composition is shown below.
Composition
[0085]
Lithium-12-hydroxystearate |
7.5 weight % |
Mineral oil (126 mm2/s @40°C) |
88.5 weight % |
Dihydrocarbyl polysulfide (sulfur content: 42 weight %) |
2.0 weight % |
Tributyl phosphite |
1.0 weight % |
Amine anti-oxidant (mixture consistency: 295) |
1.0 weight % |
Example 6
[0086] A grease composition having similar composition to that of Example 5 was prepared
in the same way as in Example 2 except that molybdenum dithiocarbamate was added.
The obtained grease composition was evaluated in the same way as in Example 1. The
result is shown in Table 1. The composition of the grease composition is shown below.
Composition
[0087]
Lithium-12-hydroxystearate |
7.5 weight % |
Mineral oil (126 mm2/s @40°C) |
84.0 weight % |
Boron nitride powders (average particle size: 5 µm) |
1.5 weight % |
Molybdenum dibutyl dithiocarbamate |
3.0 weight % |
Dihydrocarbyl polysulfide (sulfur content: 42 weight %) |
2.0 weight % |
Tributyl phosphite |
1.0 weight % |
Amine anti-oxidant (mixture consistency: 292) |
1.0 weight % |
Example 7
[0088] A grease composition having similar composition to that of Example 4 was prepared
in the same way as in Example 2 except that molybdenum dithiocarbamate was added.
The obtained grease composition was evaluated in the same way as in Example 1. The
result is shown in Table 1. The composition of the grease composition is shown below.
Composition
[0089]
Lithium-12-hydroxystearate |
7.5 weight % |
Mineral oil (126 mm2/s @40°C) |
84.0 weight % |
Boron nitride powders (average particle size: 3 µm) |
1.5 weight % |
Molybdenum dibutyl dithiocarbamate |
3.0 weight % |
Dihydrocarbyl polysulfide (sulfur content: 42 weight %) |
2.0 weight % |
Tricresyl phosphate |
1.0 weight % |
Amine anti-oxidant (mixture consistency: 290) |
1.0 weight % |
Example 8
[0090] 36.5 g of diphenylmethane-4,4'-diisocyanate were added to 350 g of mineral oil, and
the mixture was heated to 60 °C to obtain 8 homogeneous solution. Then another solution
obtained by dissolving 39.1 g of octadecyl alcohol in 250 g of the same mineral oil
by heating was added to the former solution, and the resulting mixture was agitated
vigorously. To the mixture, another solution obtained by dissolving 14.4 g of cyclohexylamine
in 195 g of the same mineral oil was added, and the obtained mixture was again agitated
vigorously to obtain a gel. The gel was kept at 100 °C°C for 30 minutes under agitation,
and admixed with the additives. The obtained mixture was agitated and passed through
a three-roll roll mill, thereby preparing a grease composition. The obtained grease
composition was evaluated in the same way as in Example 1. The result is shown in
Table 1. The composition of the grease composition is shown below.
Composition
[0091]
Thickener |
9.0 weight % |
Mineral oil (126 mm2/s @40°C) |
79.5 weight % |
Boron nitride powders (average particle size: 7 µm) |
1.5 weight % |
Molybdenum dibutyl dithiocarbamate |
3.0 weight % |
Molybdenum disulfide |
2.0 weight % |
Dihydrocarbyl polysulfide (sulfur content: 42 weight %) |
2.0 weight % |
Tributylphosphate |
2.0 weight % |
Amine anti-oxidant (mixture consistency: 314) |
1.0 weight % |
[0092] The thickener employed in this Example is a mixture of the following compounds:

wherein A stands for an N-cyclohexylamino group, B stands for an octadecyloxy group,
and the ratio of A to B in the mixture is 80 : 20.
Table 1
|
Average Life Time (hr.) |
Example 1 |
145 |
2 |
142 |
3 |
139 |
4 |
150 |
5 |
144 |
6 |
155 |
7 |
153 |
8 |
161 |
Comp. Ex. 1 |
0 |
2 |
80 |
3 |
60 |
4 |
48 |
5 |
0 |
6 |
94 |
[0093] As seen from the results in Table 1, the grease composition of the present invention
can prolong the life time of a constant velocity joint as compared to the grease compositions
shown in Comparative Examples. The life time of the joints employed in Comparative
Examples 1, 2, and 5 were over by occurrence of seizing, while that of the joins employed
in Comparative Examples 3, 4, and 6 were over by occurrence of flaking.