US2469285A - Hydraulic pressure transmitting fluid - Google Patents
Hydraulic pressure transmitting fluid Download PDFInfo
- Publication number
- US2469285A US2469285A US735527A US73552747A US2469285A US 2469285 A US2469285 A US 2469285A US 735527 A US735527 A US 735527A US 73552747 A US73552747 A US 73552747A US 2469285 A US2469285 A US 2469285A
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- United States
- Prior art keywords
- glycol
- hydraulic pressure
- fluids
- pressure transmitting
- hydraulic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000012530 fluid Substances 0.000 title description 28
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 31
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 13
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 12
- 239000004359 castor oil Substances 0.000 description 9
- 235000019438 castor oil Nutrition 0.000 description 9
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 9
- 230000001050 lubricating effect Effects 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 230000007797 corrosion Effects 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 6
- KYMJNVNKFMZBFB-UHFFFAOYSA-N N-pentylpentan-1-amine phosphoric acid Chemical compound OP(O)(O)=O.CCCCCNCCCCC KYMJNVNKFMZBFB-UHFFFAOYSA-N 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- -1 hydraulic presses Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- PDDANVVLWYOEPS-UHFFFAOYSA-N nitrous acid;n-propan-2-ylpropan-2-amine Chemical compound [O-]N=O.CC(C)[NH2+]C(C)C PDDANVVLWYOEPS-UHFFFAOYSA-N 0.000 description 4
- 230000008961 swelling Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 150000001491 aromatic compounds Chemical group 0.000 description 2
- 239000010951 brass Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229940051250 hexylene glycol Drugs 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- MWCBGWLCXSUTHK-UHFFFAOYSA-N 2-methylbutane-1,4-diol Chemical compound OCC(C)CCO MWCBGWLCXSUTHK-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- QVHMSMOUDQXMRS-UHFFFAOYSA-N PPG n4 Chemical compound CC(O)COC(C)COC(C)COC(C)CO QVHMSMOUDQXMRS-UHFFFAOYSA-N 0.000 description 1
- 241001313099 Pieris napi Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/046—Hydroxy ethers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/108—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/26—Amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/041—Triaryl phosphates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
Definitions
- the present invention relates to a new and improved hydraulic pressure transmitting fluid which, while not limited thereto, is particularly adapted for use as a hydraulic medium in hydraulic brake systems, hydraulic shock absorbers, hydraulic presses, and other fluid pressure actuated mechanism.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented May 3, 1949 HYDRAULIC PRESSURE TRANSMITTING FLUID Chester M. White, Rochester, N. Y., assignor to Genesee Research Corporation, Rochester, N. Y., a corporation of New York No Drawing. Application March 18, 1947, Serial No. 735,527
Claims. (Cl. 25278) The present invention relates to a new and improved hydraulic pressure transmitting fluid which, while not limited thereto, is particularly adapted for use as a hydraulic medium in hydraulic brake systems, hydraulic shock absorbers, hydraulic presses, and other fluid pressure actuated mechanism.
In spite of extended research in an effort to develop substitutes, castor oil is today the most commonly employed base or lubricant in hydraulic pressure transmitting fluids. Possibly the greatest drawback and disadvantage attending the use of castor oil for this purpose is its tendency to oxidize and form athick and tacky film on the moving parts of the hydraulic pressure system in which it is employed. An almost equally serious disadvantage of castor oil base fluids is their comparatively low water tolerance. Straight castor oil fluids may be separated into phases due to the presence of water of condensation.
The foregoing and other disadvantages of castor oil are obviated by the present invention and while, inone sense, the invention may be said to encompass hydraulic pressure transmitting fluids in which a new material is substituted for castor oil, it is not to be construed in such a narrow sense. The compositions of the invention are preferably free from castor oil but, when necessary, they may be readily mixed with commercial castor oil or other base fluids in com-- men use in hydraulic systems today.
According to the invention, the improved hydraulic fluids contain tricresyl phosphate as their lubricating base. By lubricating base is meant that the tricresyl phosphate comprises a substantial proportion and at least ten per cent of the hydraulic pressure transmitting fluid. It has been found that tricresyl phosphate is stable under heat and will not polymerize or gum up under hydraulic pressure use. Furthermore, it will not break down into its components, phosphoric acid and cresol, and it therefore does not exhibit corrosive tendencies to metals in the hydraulic pressure system. The discovery that tricresyl phosphate could be used as the lubricating base in hydraulic pressure transmitting fluids is indeed surprising for this reason. The decomposition of esters is one of the reasons that this class of compounds is generally not employed in brake fluid formulations. As stated above, tricresyl phosphate does not break down under conditions of use. Furthermore, it is quite surprising that this compound does not swell rubber excessively, since it is an aromatic compound, and aromatic compounds are noted for their capacity to cause rubber swelling.
Broadly stated, the hydraulic pressure transmission fluids of the present invention contain tricresylphosphate as their lubricating base,
along with solvents or diluents, and, if necessary or desirable, very small amounts of corros1on 1nhibitors, such as amine phosphates and nitrites.
As diluents 'or solvents, there may be employed, either singly or in combination one with the other,
a polymerized glycol and/or an aliphatic ether,
of a polyglycol. As used herein, the term polymerized glycol may include the specific compounds diethylene glycol, and triethylene glycol, as well as polymerized ethylene glycols having molecular weights up to 250, and the specific compounds dipropylene glycol and tripropylene glycol as well as polymerized propylene glycol. For the polymerized glycol content, there may be substituted, to the extent of not more than fifty per cent, so-called higher glycols such as butylene glycol, amylene glycol and hexylene glycol.
The alcohol ethers maybe methyl, ethyl, propyl, butyl, etc. ethers of ethylene glycol, di-
.' ethylene glycol, triethylene glycoLtetraethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol and tetrapropylene glycol. Preferably, mixtures of the foregoing alcohol ethers are employed.
The following general'formulation having the range of ingredient proportions indicated embraces a number of highly desirable fluids for.
use in hydraulic brake systems:
Per cent by weight Tricresyl phosphate (Tech.) 10-50 Polymerized glycol (single or mixed) 0-85 Aliphatic ethers of polyglycols (single or mixed) '0-85 Per cent by weight Tricresyl phosphate (Tech.) 20.00 Dipropylene glycol 40.00 Ethyl ether or triethylene glycol 39.10 Diamylamine phosphate 0.05
Diisopropylamine nitrite 0.05
3 In order to illustrate the desirability of the foregoing specific brake fluid formulation, its critical physical data is given below:
Boiling point 157 C.
Viscosity 100 F 13 1 Viscosity -40 F. 19,566 018.
Rubber swelling 0.030" (heated 5 days Cold test Clear; .flows after 11 Water tolerance water-clear and flowsafterdl days-@ -50'!.
Miscibility Castor oil base fluids" clear and -flow after 11 days 50 F. Corrosion (7 days 200 F.):
With respect to the'criticalphysical data, the
following may be observed:
Rubber-swelling 0.013 (heated 5 *days@ 158 F.)
Viscosity -.40F. -i 1902.6 0, s. Corrosion (6 days 200 F.)
Brass 0:4 mg./'sq.. cm.
Copper 0.0
Cast iron ..0.0
Steel 0:2
Aluminum-alloy 0.0
Tin 040' A still further specific example is represented by the following formulation:
Per cent by weight Tricresyl phosphate (.Tjech.) 18100 Dipropylene glycol 20.00 Ethyl ether of triethylene glycol 41.90 Ethyl ether of diethylene glycol M 20.00 Diisopropylamine nitrite 0.05 Diamylamine phosphate "0.05
The critical physical data for the foregoing formulation is as follows:
Rubber swelling(5 days 158 F.) 0.018" Corrosion (7 days (a) 158 FI) Ste'el .0.0 mg. sq. cm. Brass 0.2 Cast iron 023 Copper 0.1 Tin coated iron 0.1 Aluminum alloy 0.0
As stated, the principal advantage of the pressure transmission-fluids of .the present invention is that there is no' possibility of their oxidizing and forminga thick, tacky .film'on the moving parts of the hydraulic system. In testing the fluids for such tackiness, the following procedure was employed:
A complete wheel cylinder was assembled by lubricating the walls of the wheel cylinder, pistons, springs, and rubber cups with the fluid under test. 5100; of thelfluid wasadded to the cylinder with one port open. The cylinder was held at 70 C. for 14 days in a constant temperature oven. Examination of the cylinder and parts natthe -.endofthe"test shows no residue, gum or corrosion of any of the parts, indicating that there-was nooxidation of the ingredients.
.Aiurthen adyantage of the fluids of the pres- ;entzinvention resides in their miscibility with other commercial fluids in common usein brake systems'today. They also have good low tem- 'perature characteristics and are unusually inert astarvas rubber swelling is concerned. As a matter of fact, they do: not swell rubber at all. Intestconditionsthe diameter of arubber brake cup-isincreasedby such a. small .-amount .that it isdiificult to measurethe change with a micnometer. For. allpractical purposes it is zero: within experimental error.
The. fluids have good water tolerancehbeing;
miscible with water in all proportions. i Corrosion of the various. metalsin thehydraulics system can be held. under control by means of suitable.
inhibitors. Viscosities at.1-00..Ii?!."andv at -.40 F. establish a curve with a satisfactory slope.
What is. claimed is:
1. A hydraulic pressure fluid .consistingaessentially of the following. ingredients in the. approximate percentagesindicated:
Per. cent byweight Tricresyl phosphate 20.00 Dipropyiene glycol 14000 Ethyl ether-of. triethylene .g1ycol;. 239.10. Diamylamine phosphate 0305 Diisopropylamine nitrite 0105 2. A hydraulic pressure fluid consisting essen tially of the 'followingingredien'ts in the approximate percentages indicated:
.' Per cent by weight Trioresyl phosphate ..l 18.00 Dipropylene glycol ...I24.90 Hexylene glycol 15.00 Ethyl ether of triethylene glycol 42.00 Diisopropylamine nitrite 0.05 Diamylamine phosphate 0.05
.A. hydraulic pressure fluid consisting essentially of the following ingredients in the approximate percentages indicated:
Per cent by weight 'Ilricresyl phosphate 18.00 Dipropylene glycol 20.00 Ethyl ether oftriethylene glycol 41.90 Ethyl ether ofdiethylene glyco'l 20.00 Di-isopropylam-ine nitrite 0.05 Diamylamine phosphate 0.05
4. .A hydraulic. pressure .fluid -.consisting essential-ly of .at least 10% tricresyl phosphateas the sole lubricating base and the "remainder .at ieast onematerial. effective as a' diluent iorsaid tricresyl phosphate and selected from thengroup consisting of (1) can .alkyl ether ofua watersoluble glycol where the .alkylgroup contains 1-4 carbonatoms; (2) -a polyethylene glycol contain. ing .2-5 ethylene oxide groups; (3) apolypropylene glycol containing 2-3 propylene oxide groups; and (4) a water-soluble glycol whose alkylene group contains 4-6 carbon atoms.
5. A hydraulic pressure fluid consisting essentially of approximately 10-50% tricresyl phosphate as the sole lubricating base, approximately 50-90% of a material efiective'as a diluent for said tricresyl phosphate and selected from the group consisting of (1) an alkyl ether of a watersoluble glycol where the alkyl group contains 1-4 carbon atoms; (2) a polyethylene glycol containing 2-5 ethylene oxide groups; (3) a polypropylene glycol containing 2-3 propylene oxide groups; and (4) a water-soluble glycol whose alkylene group contains 4-6 carbon atoms, and approximately 0.1% of a corrosion inhibitor.
CHESTER M. WHITE.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US735527A US2469285A (en) | 1947-03-18 | 1947-03-18 | Hydraulic pressure transmitting fluid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US735527A US2469285A (en) | 1947-03-18 | 1947-03-18 | Hydraulic pressure transmitting fluid |
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US2469285A true US2469285A (en) | 1949-05-03 |
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US735527A Expired - Lifetime US2469285A (en) | 1947-03-18 | 1947-03-18 | Hydraulic pressure transmitting fluid |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2638180A (en) * | 1949-12-21 | 1953-05-12 | Herkimer Herbert | Air filter |
US2659699A (en) * | 1949-07-28 | 1953-11-17 | Lockheed Aircraft Corp | Hydraulic fluid of polyhydric alcohol and trialkyl phosphate |
US2732345A (en) * | 1956-01-24 | Soluble oils | ||
DE1007459B (en) * | 1952-11-10 | 1957-05-02 | Hoechst Ag | Additives to hydrostatic hydraulic fluids |
US2909489A (en) * | 1956-06-07 | 1959-10-20 | Monsanto Chemicals | Non-foaming functional fluids |
US2916457A (en) * | 1953-12-01 | 1959-12-08 | Hoechst Ag | Pressure transmitting fluids for brakes and hydraulic apparatus |
US3136726A (en) * | 1957-06-28 | 1964-06-09 | Douglas Aircraft Co Inc | Fire-resistant hydraulic fluid and lubricant |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2003429A (en) * | 1931-10-17 | 1935-06-04 | Carbide & Carbon Chem Corp | Liquid composition |
US2390258A (en) * | 1943-05-24 | 1945-12-04 | Hydraulic Brake Co | Hydraulic pressure fluid |
US2402754A (en) * | 1943-05-24 | 1946-06-25 | Hydraulic pressure fluid | |
US2419327A (en) * | 1943-06-28 | 1947-04-22 | Shell Dev | Corrosion inhibitors-nitrite salts of secondary amines |
-
1947
- 1947-03-18 US US735527A patent/US2469285A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2003429A (en) * | 1931-10-17 | 1935-06-04 | Carbide & Carbon Chem Corp | Liquid composition |
US2390258A (en) * | 1943-05-24 | 1945-12-04 | Hydraulic Brake Co | Hydraulic pressure fluid |
US2402754A (en) * | 1943-05-24 | 1946-06-25 | Hydraulic pressure fluid | |
US2419327A (en) * | 1943-06-28 | 1947-04-22 | Shell Dev | Corrosion inhibitors-nitrite salts of secondary amines |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2732345A (en) * | 1956-01-24 | Soluble oils | ||
US2659699A (en) * | 1949-07-28 | 1953-11-17 | Lockheed Aircraft Corp | Hydraulic fluid of polyhydric alcohol and trialkyl phosphate |
US2638180A (en) * | 1949-12-21 | 1953-05-12 | Herkimer Herbert | Air filter |
DE1007459B (en) * | 1952-11-10 | 1957-05-02 | Hoechst Ag | Additives to hydrostatic hydraulic fluids |
US2916457A (en) * | 1953-12-01 | 1959-12-08 | Hoechst Ag | Pressure transmitting fluids for brakes and hydraulic apparatus |
US2909489A (en) * | 1956-06-07 | 1959-10-20 | Monsanto Chemicals | Non-foaming functional fluids |
US3136726A (en) * | 1957-06-28 | 1964-06-09 | Douglas Aircraft Co Inc | Fire-resistant hydraulic fluid and lubricant |
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