[0001] The present invention relates to a fluid for use in viscous couplings and which has
high durability.
[0002] In a fluid coupling (also called a viscous coupling), a plurality of inner plates
movably disposed on a driving shaft and a plurality of outer plates fixed on a driven
shaft with predetermined spacings are combined together alternately and are accommodated
in a housing, which contains the viscous operating fluid for torque transmission.
Under such arrangement, shearing force, i.e. shear torque, is generated in said groups
of plates due to the difference of the revolutions between the driving shaft and the
driven shaft, in order to transmit torque to the driven shaft.
[0003] In recent years, organopolysiloxane oils, such as dimethylpolysiloxane or methylphenylpolysiloxane,
have been used as the hydraulic fluid or the operating fluid for fluid couplings.
[0004] A dimethylpolysiloxane (also called dimethyl-silicone oil) of high viscosity index
has been widely used, but it is difficult to maintain stable torque transmission ability
for a long period under severe operating condition at high temperature. This is mainly
due to the low thermal stability of this fluid at high temperature. Because the operating
conditions are becoming increasingly severe in various usages including in viscous
couplings, it is desirable to improve the thermal stability of the silicone oil,
which constitutes the main component of dimethyl-silicone.
[0005] To prevent oxidation or gelation, antioxidants, such as iron octanoate, phenylamine
derivatives or ferrocene derivatives, have been added to an organopolysiloxane oil.
But although a certain level of gelation preventive effect can be obtained at high
temperature when these antioxidants are added, the viscosity increases when the viscous
coupling is used continuously.
[0006] The object of this invention is to provide a fluid for viscous couplings, which has
good resistance to thermal decomposition and gelation and has high stability.
[0007] In one embodiment a fluid for viscous couplings according to the present invention
is characterized in that an organopolysiloxane is the base oil and a phosphorus type
anti-wear agent is added to it.
[0008] In the conventional type of fluid for viscous couplings, the quality of antioxidants
has been improved in order to prevent the thickening effect caused by thermal deterioration
during the operation at high temperature. But when antioxidant is added to the fluid
and it is used in a viscous coupling, the viscosity is still increased.
[0009] The present inventors have considered that this problem cannot be solved simply by
the improvement of the effect of an antioxidant and have found that the metallic contact
between disks of a viscous coupling exerts a very strong influence; it appears that
the fresh surface of the metal disk exposed due to metallic contact acts to catalyse
the deterioration of the organopolysiloxane and increases deterioration of the fluid.
[0010] By adding anti-wear agent to the fluid, a film of this agent is formed on the fresh
metal surface of metal and the catalytic effect is thus prevented. This substantially
prevents the thickening of the fluid.
[0011] With the fluid for viscous coupling according to the present invention, it is possible
to increase the heat-resistant property of the fluid and to improve its durability
by adding antioxidants together with the anti-wear agent.
[0012] It is desirable to also include in the aforesaid fluid for viscous coupling of this
invention an anti-wear agent of the sulphur and/or zinc dithiophosphate type. A phosphorus,
sulphur and zinc dithiophosphate type of anti-wear agent each has a certain effect
when each is added alone to the fluid for viscous coupling. In this invention, however,
an agent of the phosphorus, sulphur and/or zinc dithiophosphate type are admixed and
blended together, and this gives a cumulative effect to form a film on the new metal
surface and to suppress catalytic action thereby, thus almost completely eliminating
the thickening of the fluid. This provides a better effect than when a phosphorus
type agent is used alone.
[0013] The phosphorus type, sulphur type and zinc dithiophosphate type anti-wear agents
give an adsorption effect on the metal in a specific temperature range according to
their respective thermal stability. It appears that various friction and wear conditions
occur in the viscous coupling itself during the operation and that the environmental
temperature also widely differs. By this invention, the anti-wear agents with different
absorption property are combined to cope with such conditions.
[0014] By optionally adding an antioxidant to the fluid in addition to these anti-wear agents,
it is possible to increase the heat-resistant property and to improve the durability
of the fluid.
[0015] In another embodiment of the fluid of this invention, an organopolysiloxane is again
used as base oil and a metal deactivator and/or corrosion inhibitor is added.
[0016] Although a metal deactivator and/or corrosion inhibitor has lower solubility in the
coupling fluid than the anti-wear agent, these substances can prevent increase of
viscosity of the fluid when they are added in small quantity. This increases further
the heat-resistance and improves the durability of the fluid. The combined use therewith
of an anti-wear agent and/or antioxidants is also desirable, so as to increase the
heat-resistance and durability of the fluid.
[0017] An organopolysiloxane, which is the base oil of the fluid according to this invention,
has the following formula:

wherein R represents the same or different, optionally halogenated, hydrocarbon group
having 1 - 18 carbon atoms, and n is an integral number of 1 - 300.
[0018] Examples of the group R are an alkyl group such as a methyl, ethyl,
n-propyl,
i-propyl,
n-butyl,
i-butyl,
t- butyl,
n-pentyl, neopentyl, hexyl, heptyl, octyl, decyl or octadecyl group, an aryl group
such as a phenyl or naphthyl group, an aralkyl group such as a benzyl, 1-phenylethyl
or 2-phenylethyl group, an alallyl group such as an
o-,
m-,
p-diphenyl group, or a halogenated hydrocarbon group such as an
o-,
m-,
p-chlorphenyl group,
o-,
m-,
p-bromphenyl group, 3,3,3-trifluoropropyl group, 1,1,1,3,3,-3-hexafluoro-2-propyl
group, heptafluorisopropyl group or heptafluor-
n-propyl group. Particularly, it is preferable to use as R a fluorinated hydrocarbon
group having 1 - 8 carbon atoms other than an aliphatic unsaturated group; or, a mixture
of a methylpolysiloxane and phenylpolysiloxane.
[0019] In the first embodiment, there is added to the organopolysiloxane one or more of
a phosphorus type anti-wear agent. Examples thereof are those of one of the following
formulae (1) - (27) wherein R may be hydrogen, or an alkyl, aryl or benzyl group.
R may be the same or the different.

[0020] In the following, actual compounds are given for some of the formulae, namely:
[0021] Formula (1), triaryl phosphates, e.g. benzyldiphenyl phosphate, allydiphenylphosphate,
triphenyl phosphate, tricresyl phosphate, ethyldiphenyl phosphate, tributyl phosphate,
dibutyl phosphate, cresyldiphenyl phosphate, dicresylphenyl phosphate, ethylphenyldiphenyl
phosphate, diethylphenylphenyl phosphate, propylphenyldiphenyl phosphate, dipropylphenylphenyl
phosphate, triethylphenyl phosphate, tripropylphenyl phosphate, butylphenyldiphenyl
phosphate, dibutylphenylphenyl phosphate, tributylphenyl phosphate, a propyl phenyl
phenyl phosphate mixture, butyl phenyl phenyl phosphate mixture, or an acid phosphate
such as lauryl acid phosphate, stearyl acid phosphate or di-2-ethylhexyl phosphate.
[0022] Formula (2), e.g. di-
n-butylhexyl phosphate.
[0023] Formula (3), e.g.
n-butyl-n-dioctyl phosphate.
[0024] Formula (5), triaryl phosphoro-thionates, e. g. triphenyl phosphoro-thionate and
alkylaryl phosphoro-thionates
[0025] Formula (15), e.g. triisopropyl phosphite and diisopropyl phosphite.
[0026] Formula (19), e.g. trilauryl thiophosphite.
[0027] Formula (22), e.g. hexamethyl phosphoric triamide.
[0028] Formula (24), e.g. dibutyl phosphoroamidate.
[0029] Among these compounds, the effects are particularly conspicuous in the cases of the
compounds with excellent thermal stability having the structure of triaryl phosphate
or triaryl phosphoro-thionate.
[0030] Examples of the sulfur type and/or zinc dithiophosphate type anti-wear agent which
may be added now follow.
[0031] As the sulfur type of anti-wear agent, a sulfide such as diphenyl sulfide, diphenyl
disulfide, dibenzyl disulfide, di-
n-butyl sulfide, di-
n-butyl disulfide, di-
tert-butyl disulfide, di-
tert-dodecyl sulfide or di-
tert-dodecyl trisulfide, a sulfurized oil such as sulfurized sperm oil or sulfurized dipentene,
or a thiocarbonate such as xanthic disulfide; and as a zinc dithiophosphate anti-wear
agent a primary alkyl zinc dithiophosphate, secondary alkyl zinc dithiophosphate,
alkyl-aryl zinc dithiophosphate or aryl zinc dithiophosphate.
[0032] It is preferable to use each type of anti-wear agent (phosphorus type, sulfur type
and/or zinc dithiophosphate) in an amount of 0.01 - 5 wt% of the organopolysiloxane,
more preferably 0.1 - 3 wt%. The ratio of phosphorus type anti-wear agent to total
anti-wear agents is preferably 5-95 wt%.
[0033] Instead of adding a mixture of phosphorus type and sulfur type anti-wear agents,
a compound may be used containing both phosphorus and sulfur, such as having at least
one of the following formulae:

e.g. benzyl (di-
n-pentyl phosphoryl) bisulfide.
[0034] It is preferable to use these agents in amount of 0.01 - 5 wt % to the organopolysiloxane,
and more preferably, 0.1 - 3 wt %.
[0035] In another embodiment of the fluid for viscous coupling of this invention, a metal
deactivator and/or corrosion inhibitor is added to the organopolysiloxane, alone or
together with one or more of the above anti-wear agents.
[0036] As the metal deactivator, benzotriazole, benzothiazole, thiadiazole, triazole, dithiocarbamate,
indazole, or derivatives of any of these, or organic carboxylic acids including
dibasic acids such as adipic acid, sebacic acid or dodecane dioic acid, or monobasic
acids such as stearic acid, oleic acid or lauric acid, or amine salts of these compounds
may be used.
[0037] As suitable corrosion inhibitors, there are isostearate,
n-octadecylammonium stearate, a long chain aliphatic diamine e.g. DUOMEEN-T diorate,
lead naphthenate, sorbitan oleate, pentaerythrite oleate, oleyl sarcosine, alkyl succinic
acid, alkenyl succinic acid, and derivatives of these compounds.
[0038] Prefered amounts of the metal deactivator and corrosion inhibitors are each 0.001
- 1.0 wt % of the organopolysiloxane, more preferably 0.01 - 0.5 wt %. When the added
quantity exceeds 1.0 wt %, it is not desirable because precipitation increases. If
it is less than 0.001 wt %, there is no effect.
[0039] The durability of the fluid can be increased by adding antioxidant when an phosphorus
anti-wear agent is added alone, or when a phosphorus type anti-wear agent and sulfur
type anti-wear agent and/or zinc dithiophosphate type anti-wear agent are together
added, or when a metal deactivator and/or corrosion inhibitor is added alone or together
with the above anti-wear agents.
[0040] Suitable antioxidants are amine type antioxidants such as dioctyldiphenylamine, phenyl-α-naphthylamine,
alkyldiphenylamine, N-nitrosodiphenylamine, phenothiazine, N,N′-dinaphthyl-
p-phenylenediamine, acridine, N-methylphenothiazine, N-ethylphenothiazine, dipyrizylamine
and diphenylamine, phenol type antioxidants such as 2,6-di-
t-butylparacresol, 4,4′-methylenebis (2,6-di-
t-butylphenol) and 2,6-di-
t-butylphenol, or organic metal compound type antioxidants such as an organic iron
salt such as iron octoate, ferrocene or iron naphthoate, an organic cerium salt such
as cerium naphthoate or cerium toluate, and an organic zirconium salt such as including
zirconium octoate. The above antioxidants may be used alone or in a combination of
two or more compounds to provide cumulative effects.
[0041] Preferred amounts of the antioxidants are 0.001 - 5 wt % of the organopolysiloxane,
more preferably 0.01 - 2 wt %.
[0042] The invention will now be illustrated by reference to specific examples. Viscosities
were measured at 25°C.
Example 1
[0043] To dimethylisilicone (viscosity 50,000 mm²/s) tricresyl phosphate was added in the
percentages shown below (none in control samples) as phosphorus type anti-wear agent;
some samples (a) also contained 1.0 wt % of diphenylamine as antioxidant. Each fluid
for viscous coupling thus prepared was filled into a viscous coupling having 111
disks at 25°C and at a filling degree of 85 vol %. The difference in speeds of rotation
was 50 rpm.
[0044] The viscous coupling was placed in a bath kept at a constant temperature of 130°C
and was operated for 50 hours.
[0045] After the operation, the viscosity change and torque change were measured; the results
are given in the table below
[0046] To evaluate the heat-resistant property of the anti-wear agent, a hot tube coking
test was performed, and the temperature at which the specimen was gelated or blocked
by coking in the glass tube was measured at every 10°C. The lowest temperature is
also shown in the table below.
| Added quantity of anti-wear agent (wt %) |
Viscosity change (%) |
Torque change (%) |
Blocking temperature (°C) |
| (a) with diphenylamine antioxidant |
| 2.0 |
-5 |
-5 |
330 |
| 1.0 |
+1 |
0 |
330 |
| 0.5 |
+5 |
+5 |
330 |
| 0 |
Measurement not achievable |
Measurement not achievable* |
330 |
| (b) without antioxidant |
| 2.0 |
-3 |
-3 |
290 |
| 1.0 |
+1 |
+1 |
290 |
| 0.5 |
+6 |
+5 |
290 |
| 0 |
Measurement not achievable |
Measurement not achievable |
290 |
Example 2
[0047] Example 1 was repeated, but with various amounts of tricresyl phosphate (A) and triphenyl
phosphorothionate (B) as phosphorus type anti-wear agents in the weight percentage
shown below. The four fluids thus prepared were tested as in Example 1; the results
are given in the table below:
| (A) Added quantity |
(B) Added quantity |
Viscosity change (%) |
Torque change (%) |
Blocking temperature (°C) |
| a) with antioxidant in the fluid |
| 0 |
1.0 |
+2 |
+1 |
330 |
| 0.5 |
0.5 |
+1 |
0 |
330 |
| b) without antioxidant |
| 0 |
1.0 |
+1 |
+1 |
290 |
| 0.5 |
0.5 |
+3 |
+3 |
290 |
[0048] Examples 1 and 2 show that satisfactory fluids can be prepared even when antioxidant
is not added.
Comparative example1
[0049] To dimethylsilicone (viscosity 50000 mm²/s) 1.0 wt % of diphenylamine was added as
antioxidant (in samples (a)) and dibenzyl disulfide was added as sulfur type anti-wear
agent in the percentage shown below. The fluids thus prepared were tested by as in
the Embodiment 1 and the results were:
| Added quantity of anti-wear agent (wt %) |
Viscosity change(%) |
Torque change(%) |
Blocking temperature (°C) |
| (a) with antioxidant |
| 1.0 |
-2 |
-2 |
300* |
| 0.5 |
+5 |
+7 |
310* |
| 0 |
Measurement not achievable |
Measurement not achievable |
320 |
| (b) without antioxidant |
| 2.0 |
-3 |
-4 |
250* |
| 1.0 |
+1 |
0 |
250* |
| 0.5 |
+7 |
+7 |
260* |
| 0 |
Measurement not achievable |
measurement not achievable |
290 |
[0050] As is evident from this comparative example, both sulfur type and phosphorus type
agents have almost the same torque stability as anti-wear agents in the fluid. However,
because the heat-resistance of the additive itself is inferior to that of the organopolysiloxane,
the coking phenomenon occurs, in which black decomposed products of the additive are
generated in the hot tube coking test, and the thermal stability of the fluid is thus
reduced by the addition of such agent.
Examples 3 to 5
[0051] To dimethylsilicone (viscosity 100,000mm²/s) one of three specified phosphates was
added as phosphorus type anti-wear agent in the percentages given below (none for
a control sample). Each fluid for viscous coupling thus prepared was used in a coupling
as in Example 1 but the rotating speed difference was 25 rpm and the bath temperature
was 170°C, with the following results:

Comparative Examples 2 and 3
[0052] Example 3 was repeated but using dibenzyl disulfide and a polysulfide respectively
as sulfur type anti-wear agents instead of the phosphorus type anti-wear agent tricresyl
phosphate. The results are:

[0053] It is evident from these comparative examples that both phosphorus type and sulfur
type agents exhibit excellent durability in viscosity change and torque change of
the fluid for viscous coupling when the temperature is relatively low as in the Examples
1 and 2 and Comparative Example 1, whereas the phosphorus type shows the higher durability
at high temperature. This is attributable to the fact that, because a sulfur type
anti-wear agent was a lower heat-resistant property, the reaction with dimethylsilicone
or with the plates in the viscous coupling proceeded excessively at high temperature,
which the phosphorus type anti-wear agent was higher heat-resistant property.
[0054] As for the odor of the coupling fluids that of Example 3 is odorless and did not
have a strong sulfur odor as did the fluids of the comparative examples. A phosphorus
type of anti-wear agent is thus more convenient in use than a sulfur type anti-wear
agent.
Example 6 and Comparative Examples 4 and 5
[0055] To dimethylsilicone (viscosity 50,000 mm²/s) there was added a phosphorus type anti-wear
agent according to the invention or one of two sulfur type anti-wear agents (for comparison)
each in the percentages below. Each of the six fluids thus prepared was filled into
an autoclave at 25°C at a filling degree of 80 vol %. After replacing the remaining
air with nitrogen, it was placed at 200°C in a thermostat for 24 hours.
[0056] After the test, the viscosity change was measured, and the results were:
| Ex No |
Agent |
Added quantity of anti-wear agent (wt%) |
Viscosity change (%) |
| 6 |
triphenyl phosphate |
2.0 |
-1 |
| 1.0 |
±0 |
| Comp 4 |
dibenzyl disulfide |
2.0 |
-27 |
| 1.0 |
-18 |
| Comp 5 |
a polysulfide |
2.0 |
-17 |
| 1.0 |
-12 |
[0057] From the above comparative Examples 4 - 5, it is seen that the sulfur type anti-wear
agents having lower heat-resistant property were deteriorated, and this apparently
induced the viscosity decrease and the deterioration of the dimethylsilcone.
[0058] By contrast, the phosphorus type agent in Example 6 was stable to dimethylsilicone
and this may be attributed to the high heat-resistant property of thus agent.
Example 7
[0059] To dimethylsilicone (viscosity 100,000 mm²/s) of tricresyl phosphate (phosphorus
type) and dibenzyl disulfide (sulfur type) were added together and separately (for
comparison) in the percentages below as anti-wear agents. In a series (a) of samples,
1.0 % of diphenylamine was also added as antioxidant. The fluid for viscous coupling
thus prepared was filled into a viscous coupling having 111 iron disks at 25°C and
at a filling degree of 85 vol %. The rotating speed difference was 35 rpm.
[0060] The viscous coupling was maintained in a bath kept at constant temperature of 130°C
and was operated for 100 hours.
[0061] After the operation, viscosity change and torque change were measured. The results
are given in the table below together with the results of the iron quantity, measured
as wear fragment quantity.
| Added quantity of phosphorus type (wt %) |
Added quantity of sulfur type (wt %) |
Viscosity change (%) |
Torque change (%) |
Wear fragment iron (ppm) |
| (a) with antioxidant |
| 0.5 |
0 |
+5 |
+5 |
450 |
| 0 |
0.5 |
+7 |
+5 |
480 |
| 0.25 |
0.25 |
+1 |
0 |
120 |
| (b) without antioxidant |
| 0.5 |
0 |
+5 |
+5 |
470 |
| 0 |
0.5 |
+5 |
+5 |
430 |
| 0.25 |
0.25 |
+1 |
+1 |
130 |
[0062] It is evident from the results that the viscosity change and torque change as well
as amount of wear fragment iron are increased more in the case where two anti-wear
agents are simultaneously added to the fluid for viscous coupling than when only one
of the anti-wear agents is added: and that the results are simular even without antioxidant
[0063] In a coupling fluid to which both of the above phosphorus type and sulfur type anti-wear
agents were added, 0.20 wt % di-sec-butyl zinc dithiophosphate (zinc dithiophosphate
type) was added. The fluid thus prepared was tested by the same procedure as above.
As the result, the viscosity change was +1%, torque change was 0%, and wear fragment
iron quantity was 140 ppm. Thus, an excellent fluid for viscous coupling can be obtained
by combining phosphorus type, sulfur type and zinc dithiophosphate type anti-wear
agents.
Example 8
[0064] In the specimen of Example 7, sulfurized sperm oil was added in the percentages given
below as sulfur type anti-wear agent instead of dibenzyl disulfide (sulfur type) anti-wear
agent. The fluid thus prepared was tested as in Example 7 and the results were:
| Added quantity of phosphorus type (wt %) |
Added quantity of sulfur type (wt %) |
Viscosity change (%) |
Torque change (%) |
Wear fragment iron (ppm) |
| 0 |
0.5 |
+5 |
+7 |
450 |
| 0.25 |
0.25 |
+3 |
+3 |
200 |
[0065] Also when a sulfurized olefin was used instead of the sulfurized sperm oil, similar
results were obtained.
Example 9
[0066] In the specimen of Example 7, an aminedibutyl phosphonate (phosphorus type agent)
anti-wear agent was added in the percentages given below instead of tricresyl phosphate
(phosphorus type) anti-wear agent. The fluid was tested as in Example 7, and the results
were:
| Added quantity of phosphorus type (wt %) |
Added quantity of sulfur type (wt %) |
Viscosity change (%) |
Torque change (%) |
Wear fragment iron (ppm) |
| 0.5 |
0 |
+7 |
+5 |
450 |
| 0.25 |
0.25 |
+1 |
+1 |
200 |
Example 10
[0067] In the specimen of Example 7, di-sec-butyl zinc dithiophosphate (zinc dithiophosphate
type amount) was added in the percentages below instead of dibenzyl disulfide (sulfur
type). The fluid thus prepared was tested as in Example 7, and the results were:
| Added quantity of phosphorus typ (wt %) |
Added quantity of zinc thiophosphate (wt %) |
Viscosity change (%) |
Torque change (%) |
Wear fragment iron (ppm) |
| 0 |
0.5 |
+8 |
+7 |
350 |
| 0.25 |
0.25 |
+3 |
+3 |
250 |
Example 11
[0068] In the fluid of Example 7, triphenyl phosphorothionate (phosphorus type) anti-wear
agent was added in the percentage as given below instead of tricresyl phosphate (phosphorus
type) anti-wear agent. The fluid prepared was tested as in Example 7, and the results
were:
| Added quantity of phosphorus type (wt %) |
Added quantity of sulfur type (wt %) |
Viscosity change (%) |
Torque change (%) |
Wear fragment iron (ppm) |
| 0.5 |
0 |
+5 |
+3 |
350 |
| 0.25 |
0.25 |
+1 |
0 |
130 |
Example 12
[0069] To dimethylsilicone (viscosity 50,000 mm²/s) 0.5 wt % of phenyl-α-naphthylamine was
added as antioxidant and benzothiazole was added as metal deactivator, and triphenyl
phosphate as anti-wear agent in the percentages given below. The fluid thus prepared
was filled into a viscous coupling having 111 disks at 25°C and at a filling degree
of 85 vol %. The rotating speed difference was 50 rpm.
[0070] The viscous coupling was placed in a bath at constant temperature of 130°C and was
operated for 100 hours. After the operation, viscosity change and torque change were
measured; the results were:
| Anti-wear agent (wt %) |
Metal deactivator (wt %) |
Viscosity change (%) |
Torque change (%) |
| 0 |
0 |
Measurement not achievable* |
Measurement not achievable* |
| 0 |
0.1 |
+10 |
+10 |
| 0 |
0.4 |
+8 |
+7 |
| 0 |
0.8 |
+5 |
+5 |
| 0.5 |
0.1 |
+2 |
+2 |
| * Stopped before the expiration of 100 hours due to sudden increase of torque. |
Example 13
[0071] To dimethylsilicone (viscosity 50,000 mm²/s) 1.0 wt % of diphenylamine was added
as anti-oxidant, benzotriazole was added as metal deactivator, and tricresyl phosphate
was added as anti-wear agent, and in the percentages given below in one series (a)
of samples 1.0 wt % of diphenylamine was added as antioxidant. Each fluid was tested
as in Example 12 with the results:
| Anti-wear agent (wt %) |
Metal deactivator (wt %) |
Viscosity change (%) |
Torque change (%) |
| (a) with antioxidant |
| 0 |
0 |
Measurement not achievable* |
Measurement not achievable* |
| 0 |
0.1 |
+8% |
+8% |
| 0 |
0.4 |
+5% |
+5% |
| 0 |
0.8 |
+3% |
+3% |
| 0.5 |
0.1 |
±0 |
±0 |
| (b) without antioxidant |
| 0 |
0 |
Measurement not achievable |
Measurement not achievable |
| 0 |
0.1 |
+10% |
+10% |
| 0 |
0.4 |
+7% |
+5% |
| 0 |
0.8 |
+5% |
+4% |
| 0.5 |
0.1 |
+2% |
±0% |
| * Measurement stopped before the expiration of 100 hours due to sudden increase in
torque. |
Example 14
[0072] In each specimen of Example 13, a corrosion inhibitor n-octadecyl ammonium stearate
was added in the percentage given below instead of the metal deactivator. Each fluid
sample was tested as in Example 13, and the results are below. In the table, the added
quantity of the anti-wear agent is not given.
| Added quantity of corrosion inhibitor (wt%) |
Viscosity change (%) |
Torque change (%) |
| 0 |
Measurement not achievable |
Measurement not achievable |
| 0.1 |
+12% |
+12% |
| 0.4 |
+8% |
+10% |
| 0.8 |
+4% |
+5% |
| 0.1 |
+3% |
+3% |
| (b) without antioxidant |
| 0 |
Measurement not achievable |
Measurement not achievable |
| 0.1 |
+14% |
+14% |
| 0.4 |
+10% |
+10% |
| 0.8 |
+5% |
+6% |
| 0.1 |
+3% |
+3% |
Example 15
[0073] Example 13, was repeated but the amount of the metal deactivator was 0.1 wt % and
the corrosion inhibitor 0.2 wt %. The viscosity change was ±0%, and torque change
was +3%.