Background Of Invention
[0001] This invention relates to a hydraulic fluid. More specifically, this invention relates
to a hydraulic fluid whose principal agent comprises a methylpolysiloxane oil with
a specific gravity of 1.02 or greater at 25°C. This invention also relates to a process
of transmitting power from one place to another via a hydraulic fluid medium where
the hydraulic fluid medium is a methylpolysiloxane oil with a specific gravity of
1.02 or greater at 25°C.
[0002] Glycol ether base agents are typical examples of convention hydraulic oils used in
automotive brake and clutch systems. The drawbacks of a glycol ether base hydraulic
oil include the significant decline in both the boiling point and the temperature
at which vapor lock occurs when the hydraulic fluid contains water either absorbed
from the environment or introduced by accident. In order to eliminate these drawbacks,
a large number of hydraulic oils with a silicone oil principal agent or base have
been proposed to date. In particular, dimethylsilicone oils have been recognized as
a hydraulic fluid and in particular as an automotive brake fluid because they exhibit
a relatively insignificant variation in viscosity over a wide range of temperatures,
a low solidification temperature and a high boiling point.
[0003] One important property required of a brake fluid, which comprises a major application
of hydraulic fluids, is that the brake fluid can dissolve at least some quantity of
water without separation or settling. With a brake fluid that can not dissolve any
water, water mixed into the brake fluid accumulates in the lower regions of the pipe
system of the operating mechanism and causes corrosion of the pipe system or solidifies
in winter with a resulting loss of braking ability. The solubility of water in a dimethylsilicone
oil is much lower than in a glycol ether system. Dimethylsilicone oil usually absorbs
and dissolves at most 0.1 weight - percent water. For this reason, when the water
content- is larger than the amount of a dimethylsilicone oil is capable of absorbing,
the water is dispersed into the dimethylsilicone oil and eventually settles in the
lower regions of the operating mechanism because the specific gravity of a dimethylsilicone
oil is about 0.96 which is less than the specific gravity of 1.0 for water. In such
a case the dimethylsilicone oi! will no longer function satisfactorily as a brake
fluid. In order to eliminate the above drawbacks, U.S. Patent No. 3,725,287 (issued
April 3, 1973) and Japanese Patent No. 53-21476 (78-21476) attempt to impart hydrophilici..ty
by chemically modifying the dimethylsilicone oil. These attempts can increase the
water absorptivity but require a special silicone starting material and are therefore
disadvantageous from the standpoint of cost. Furthermore, the modified silicone are
chemically unstable.
The Invention
[0004] The present invention relates to a hydraulic fluid comprising a methylpolysiloxane
oil containing siloxane units of general formula (CH
3)
aSiO
(4-a)/2 where a is 1, 2, or 3 wherein said methylpolysiloxane oil has a specific gravity
of 1.02 or greater at 25°C. The present invention also relates to a process of transmitting
power from one place to another via a hydraulic fluid medium where the hydraulic fluid
medium comprises a methylpolysiloxane oil containing siloxane units of general formula
(CH
3)
aSiO
(4-a)/2 where a is 1, 2, or 3 wherein said methylpolysiloxane oil has a specific gravity
of 1.02 or greater at 25°C.
[0005] The methylpolysiloxane oil of the present invention may be constituted of a single
unit or of a combination of two or all three units from among CH
3SiO
3/2, (CH
3)
2SiO and (CH
3)
3SiO
1/2 siloxane units. However, it must exhibit a specific gravity of
*1.02 at 25°C and be an oil at room temperature. Under these restrictions, the following
four combinations are practical: CH
3SiO
3/2 units, alone; CH
3SiO
3/2 units and (CH3)2SiO units; CH
3SiO
3/2 units and (CH
3)
3SiO
1/2 units; CH
3SiO
3/2 units, (CH
3)
2SiO units and (CH
3)
3SiO
1/2 units. From the standpoint of ease of synthesis, the CH
3SiO
3/2 unit and (CH
3)
2SiO unit as well as the CH
3SiO
3/2 unit, (CH
3)
2SiO unit and (CH
3)
3SiO
1/2 unit comb.inations are preferred. In these cases, the methylpolysiloxane is generally
a liquid at room temperature and generally exhibits a specific gravity of
*1.02 for a molar ratio of CH
3SiO
3/2 units and (CH
3)
2SiO units in the range of 1:9 to 6:4.
[0006] Preferred methylpolysiloxane oils contain 0 to 10 mol percent (CH
3)
3SiO
1/2 units, 45-80 mol percent (
CH
3)
2SiO units, and 20-45 mol percent CH
3SiO
3/2 units. Preferred methylpolysi loxane oils also generally have a CH
3/Si ratio in the range of 1.65 to 1.80 in order to jnsure the specific gravity of
the methylpolysiloxane is consistently greater than or equal to 1.02. Generally, if
the CH
3lSi ratio is significantly outside the 1.65 to 1.80 range the methylpolysiloxane will
either have too low a specific gravity or too high a viscosity to be useful as the
hydraulic fluid of this invention.
[0007] The oxygen atoms in the CH
3SiO
3/2 and (CH
3)
2SiO units of the methylpolysiloxanes used in this invention will normally be in the
form of siloxane bonds. Some of these oxygen atoms may however be in the form of hydroxyl
or alkoxy groups. The molecule structure of the methylpolysiloxane may be network,
cage, or branched chain configuration. To be most useful the hydraulic fluid of this
invention should have a viscosity in the range of 10 to 10,000 cSt at 25°C.
[0008] The methylpolysiloxane oils of this invention may be readily produced by methods
well known in the art. For example, these methylpotysiloxanes may be produced by the
homo-hydrolytic or co-hydrolytic polycondensation of methylpolysiloxanes or methylalkoxysilanes.
Preferred methylchlorosilanes include methyltrichlorosilane, dimethyldichlorosilane,
and trimethylchlorosilane. Preferred methylalkoxysilanes include the methylmethoxysilanes
and the methylethoxysilanes such as methyltrimethoxysilane, methyltriethoxysilane,
dimethyldimethoxysilane, dimethyldiethoxysilane, trimethylmethoxysilane, and trimethylethoxysilane.
The amounts of the various methylhalosilanes or methylalkoxysilanes used in the preparation
of the methylpolysiloxane oil will be determined by the desired amounts of CH
3SiO
3/2, (CH
3)
2SiO, and (CH
3)
3SiO
1/2 units in the methylpolysiloxane which will in turn determine the specific gravity
and viscosity of the hydraulic fluid. An organic solvent which can dissolve these
silanes is preferably added in hydrolytic polycondensation. When an excess of silicon-bonded
hydroxyl and alkoxyl groups remains after hydrolytic polycondensation, the polycondensation
reaction is preferably continued at an elevated temperature under reduced pressure
in order to significantly reduce the levels of these functional groups.
[0009] The hydraulic oil of this invention may contain only a methylpolysiloxane oil or
may optional ly contain various additives. The various additives include dialkanol
esters of dibasic acids (as rubber swell agents or lubricants), e.g., dioctyl sebacate,
dihexyl adipate, trialkyl phosphates such as tributyl phosphate and trioctyl phosphate
and corrosion inhibitors such as zinc naphthenate. Other conventional additives may
also be used. These additives may comprise about 0.01 to 10 weight percent of the
quantity of the methylpolysiloxane Oil.
[0010] Even if water is mixed into the hydraulic oil of this invention it can be readily
separated and removed since it forms the upper layer. This oil is a satisfactory hydraulic
oil and in particular a satisfactory brake fluid because it exhibits an insignificant
change in viscosity over a wide temperature range, a low solidification temperature,
a high boiling point, as well as chemical stability.
[0011] This invention is illustrated in the following example which is not intended to limit
the invention. In the example, the viscosity and specific gravity were both measured
at 25°C.
Example
[0012] Trimethylchlorosilane (220 g, 2.0 moles), dimethyldichlorosilane (4,515 g, 35.0 moles),
methyltrichlorosilane (1.944 g, 13.0 moles) and toluene (2,000 g) were charged to
a 10 L three-necked flask equipped with stirrer, addition funnel and reflux condenser.
Water (810 g, 45 moles) was added dropwise over 3 hours with stirring temperatures
of
*50
PC. The vigorous evolution of hydrogen chloride was observed. After addition of the
water, the mixture was heated to 60°C and then reacted for 1 hour. The reaction solution
was combined with 2 L of water, stirred and then allowed to stand and the aqueous
layer was subsequently removed. This washing procedure was conducted three times in
order to remove residual hydrochloride from the methylpolysiloxane-containing layer.
The methylpolysiloxane containing layer was then heated in order to remove water azeotropically
with toluene. Toluene was removed by raising the temperature to 150°C.
[0013] The resulting methylpolysiloxane had a viscosity of 12.6 cSt and a specific gravity
of 0.991. This methylpolysiloxane was combined with 30 g of acid clay and stirred
at 120°C for 5 hours. The generation of water by polycondensation of silanol group
bonds in the methylpolysiloxane was observed. After cooling, the reaction solution
was combined with 50 g diatomaceous earth as a filter aid and then filtered under
increased pressure. The filtrate was subjected to reduced pressure to remove low-boiling
compounds. Finally, volatiles were removed at a temperature of 240°C under a reduced
pressure of 10mm Hg. The product methylpolysiloxane oil (referred to hereafter as
A) was colorless and transparent with a viscosity of 56 cSt and a specific gravity
of 1.026. Component analysis by Si
29-NMR spectroscopy indicated that this methylpolysiloxane oil contained 4 mol percent
of (CH
3)
3SiO
1/2 units, 71 mol percent of (CH
3)
2SiO units, and 25 mol percent of CH
3SiO
3/2 units. The methylpolysiloxane (A) had a 1.7
9 Me/Si ratio.
[0014] A co-hydrolytic polycondensation of methyltrichlorosilane (790 g, 5.3 moles), dimethyldichlorosilane
(682 g, 5.3 moles) and trimethylchlorosilane (2,170 g, 20 moles) was prepared by a
method identical to that used for methylpolysiloxane oil (A) to produce methylpolysiloxane
oil (B) with a viscosity of 744 cSt and a specific gravity of 1.084. The co-hydrolytic
polycondensation of methyltrichlorosilane (225 g, 1.8 moles) and dimethyldichlorosilane
(775 g, 6.0 moles) was similarly conducted to produce methylpolysiloxane oil (C) with
a viscosity of 65 cSt and a specific gravity of 1.021. Component analyses by Si
29-NMR spectroscopy indicated that methylpolysiloxane oil (B) contained 10 mol percent
of (CH
3)
3SiO
1/2 units, 45 mol percent of (CH
3)
2SiO units, and 45 mole percent of CH
3SiO
3/2 units and that methylpolysiloxane oil (C) contained 80 mol percent (CH
3)
2SiO units and 20 mol percent of CH
3SiO
3/2 units. The CH
3/Si ratios for methylpolysiloxane oils (B) and (C) was 1.65 and 1.80, respectively.
[0015] For comparison purposes a dimethylsilicone oil (D) was prepared by the same procedure
described above. The dimethylsiloxane oil (D) consisted of (CH
3)
3SiO
1/2 units (4 mol percent) and (CH
3)
2SiO units (96 mol percent). The dimethylsiloxane oil (D) had a Me/5i ratio of 204,
a specific gravity of 0.96, and a viscosity of 50 cSt.
[0016] Each of these methylpolysiloxane oils (A), (B) and (C) and the dimethylsiloxane oil
(D) was separately combined with 5 weight percent distilled water, agitated by shaking
for 10 minutes and allowed to stand for 30 minutes in order to examine the water-oil
separation. In the cases of the methylpolysiloxane oils (A), (B), and (C) the water
and siloxane oil underwent complete separation with the water forming the upper layer.
For the dimethylsiloxane oil (D) separation was observed with water forming the lower
level.
[0017] Methylpolysiloxane oil (A) was examined at low temperatures for water resistance
according to a test method for automotive brake fluids Japanese Industrial Standard
(JIS) K2233. One hundred milliliters of methylpolysiloxane oil (A) was placed in a
centrifuge tube to which was added 3.5 ml of distilled water. After shaking for 10
minutes the sample was allowed to settle for 5 minutes at which time the sample was
cooled to -40°C. The sample remained at -40°C for 120 hours. After completion of the
test the methylpolysiloxane oil (A) was found to have remained transparent. The water,
which was totally located above the siloxane oil (A), was frozen. The test tube was
then turned upside down. An air bubble reached the surface of the siloxane oil in
about 5 seconds. Test method JIS K2233 requires that such an air bubble reach the
surface of the test brake fluid in a time of less than 10 seconds. For comparison
purpose a similar test was performed on dimethylsiloxane (D). After completion of
this test a part of the water was found to have solified within the siloxane oil (D)
and remain suspended therein and a part of the solified water had settled out.
[0018] The above comparison demonstrates that a brake fluid whose principal agent is methylpolysiloxane
oil as described in this invention will not cause corrosion of the pipe system or
vapor locking even when a large amount of water is mixed into the pipe system of the
operating mechanism. This is due to the fact that water separates in the upper part
of the brake system's master cylinder and can therefore be easily removed.
[0019] The metal corrosiveness and styrene butadiene rubber (SBR) swell of methylpolysiloxane
oil (A) and dimethylsilicone oil (D) were also evaluated by the methods of JIS K2233.
Each oil was combined with tributyl phosphate (5 weight percent) as a rubber shrinkage
inhibitor before testing. Metal corrosiveness was determined using a clean panel (80
x 13 mn) of the appropriate metal. The metal panel was placed in the siloxane oil
at 100°C for 120 hours and any changes in weight were noted. The rubber swell was
determined by immersing the SBR cup at either 70 or 120°C for 70 hours.-The cup was
washed with ethanol and the physical properties determined. The results are reported
in Tables 1 and 2. As compared with dimethylsilicone oil (D), methylpolysiloxane oil
(A) satisfied the properties of an automotive brake fluid in every measured respect.

1. A hydraulic fluid comprising a methylpolysiloxane oil containing siloxane units
of the general formula (CH3)aSiO(4-a)/2 where a is 1, 2, or 3 and wherein said methylpolysiloxane oil has a specific gravity
of 1.02 or greater at 25°C.
2. A hydraulic fluid as described in claim 1 wherein said methylpolysiloxane oil has
a viscosity of 10 to 10,000 cSt at 25°C.
3. A hydraulic fluid as described in claim 2 wherein said methylpolysiloxane oil contains
(CH3)3SiO1/2 units, (CH3)2SiO units, and CH3SiO3/2 units.
4. A hydraulic fluid as described in claim 2 wherein said methylpolysiloxane oil contains
(CH3)2SiO units and CH3SiO3/2 units.
5. A hydraulic fluid as described in claim 2 wherein said methylpolysiloxane oil contains
0 to 10 mol percent (CH3)3SiO1/2 units, 45-80 mol percent (CH3)2SiO units, and 20-45 mol percent CH3SiO3/2 units.
6. A hydraulic fluid as described in claim 2 wherein said methylpolysiloxane oil has
a CH3/Si ratio of 1.65 to 1.80.
7. A hydraulic fluid as described in claim 3 wherein said methylpolysiloxane oil has
a CH3/Si ratio of 1.65 to 1.80.
8. A hydraulic fluid as described in claim 4 wherein said methylpolysiloxane oil has
a CH3/Si ratio of 1.65 to 1.80.
9. A hydraulic fluid as described in claim 5 wherein said methylpolysiloxane oil has
a CH3/Si ratio of 1.65 to 1.80.
10. In a process of transmitting power from one place to another via a hydraulic fluid
medium, characterized by using as the hydraulic fluid medium a hydraulic fluid comprising
a methylpolysiloxane oil containing siloxane units of general formula (CH3)aSiO(4-a)/2 where a is 1, 2, or 3 wherein said methylpolysiloxane oil has a specific gravity
of 1.02 or greater at 25°C.