US2947699A - Non-inflammable hydraulic fluid - Google Patents
Non-inflammable hydraulic fluid Download PDFInfo
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- US2947699A US2947699A US534386A US53438655A US2947699A US 2947699 A US2947699 A US 2947699A US 534386 A US534386 A US 534386A US 53438655 A US53438655 A US 53438655A US 2947699 A US2947699 A US 2947699A
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- 239000012530 fluid Substances 0.000 title description 17
- 239000000344 soap Substances 0.000 claims description 22
- 239000002253 acid Substances 0.000 claims description 18
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 14
- 150000001336 alkenes Chemical class 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 238000005810 carbonylation reaction Methods 0.000 claims description 4
- 229910017052 cobalt Inorganic materials 0.000 claims description 4
- 239000010941 cobalt Substances 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 3
- 230000006315 carbonylation Effects 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 9
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- 239000002562 thickening agent Substances 0.000 description 7
- 239000002585 base Substances 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 231100000241 scar Toxicity 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 229920000151 polyglycol Polymers 0.000 description 3
- 239000010695 polyglycol Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000002199 base oil Substances 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 101500021084 Locusta migratoria 5 kDa peptide Proteins 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000013556 antirust agent Substances 0.000 description 1
- 239000003637 basic solution Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- -1 for example Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000010720 hydraulic oil Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 150000004715 keto acids Chemical class 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000001706 oxygenating effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000003405 preventing effect Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000005480 straight-chain fatty acid group Chemical group 0.000 description 1
Classifications
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- 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
- C10M173/00—Lubricating compositions containing more than 10% water
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
-
- 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- 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
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/122—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
-
- 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
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- 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
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more 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
- 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
- C10M2209/107—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106
-
- 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
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
-
- 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
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
-
- 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
-
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/01—Emulsions, colloids, or micelles
Definitions
- water base hydraulic fluids have relatively very poor lubricating characteristics.
- tent Patented Aug. 2, 1960 2 corresponding fatty oils or glycerides and the like, in mineral base oils to reduce wear and also to help inhibit rust is well known. These materials, however, are sub stantially insoluble in water base hydraulic oils or fluids and are, therefore, unsuitable for use in the compositions of the present invention.
- a combination of glycol-water base fluid may be blended with a polyglycol or polyglycolether type polymeric thickener to improve viscosity and viscosity index, and a water soluble soap of an organic aliphatic acid may be used to impart the other required properties.
- a water soluble soap preferably an alkali metal soap of a moderately long chain aliphatic acid, shows exceptional utility as an anti-wear and anti-rust agent.
- the alkali metal soaps of straight chain fatty acids of C chain length or longer are substantially insoluble in Water.
- the branched chain soaps, however, of acids having from at least 7 carbon atoms up to about 14 carbon atoms are soluble in water, and soaps of highly branched acids up to about C are soluble in the composi tions of this invention. They may be used to form stable blends having good wear preventing properties,
- Operable catalysts include the Well known cobalt containing catalysts, for example, cobalt, stearate, cobalt carbonyl, and the like. Pressures ranging from about 100 to about 300 atmospheres are used and a temperature in the rangeof about 200 to about 400 F.
- the ratio of hydrogen to carbon monoxide employed may vary betweenabout 0.5 volume to 2.0, volumes of hydrogen 'per volume of carbon monoxide.
- the olefinic starting material preferably comprises olefins having frorn 8 to 12 carbon atoms per molecule,
- olefins having from 6 to; 24 carbon atoms may 1 be used.
- the olefin is carbonylated in the process and r the resulting aldehyde hasone more carbon atom the starting olefin.
- the aldehyde resulting from the carbonylat-ion of the olefin is .then oxidized to obtain the desired branched chain acid.
- This reaction is brought about by subjecting the aldehyde in basic solution to the action of an oxygenating substance suchiasa; mixture ofnitrogen and oxygen (a irj)',. a material. releasing Enasc ent oxygen (KMnQ or thelike; 'Theoxidation reaction, one which is well known in the art, proceeds in accordance with the following equation:
- the Oxo reaction may be carried out in the presence of water in the form of vapor instead of hydrogen.
- the desired branched chain acid is thus ob tained directly from the x0 process.
- the same conditions of temperature and pressure are necessary for this reaction as for the carbonylation reaction resulting in the aldehyde as described above.
- a preferred composition consists of about 40 to 65% by weight of water, about 9 to 34% of ethylene glycol, 20 to 30% of a polyglycol or polyglycolether thickener of sufficiently high molecular weight to increase the viscosity substantially, and 0.5 to 2% of the sodium soap of Oxo or other branched chain acids of the C to C range.
- the potassium soaps may be substituted for the sodium soaps and the proportion of water to ethylene glycol may be varied considerably depending upon the viscosity, pour point, freezing point, or other requirements.
- EXAMPLE I A fluid containing 62.9% by weight of water, 11.1% of ethylene glycol, 25% of a polymeric glycolether having a viscosity of about 90,000 S.U.S. at 100 F., sold by Union Carbide and Carbon Chemical Corp., under the trade name Ucon 75 H-90,000 1 was modified by addition of 1% of the sodium soap of a C 0x0 acid. This product had a viscosity of 290 S.U.S. at 100 F. and a viscosity index of 162.
- EXAMPLE II A composition was prepared exactly as above except that 1% of sodium soap of 0,, 0x0 acid was used as the modifier. Comparative lubrication tests were made using the 4-ball wear tester wherein three ball bearings, onehalf inch in diameter, are clamped in a holding device and a fourth ball is rotated so as to bear on the first three under an applied load. This test of steel on steel was conducted at 167 F. under a 10 kg. load for one hour. In this test a glycol water base fluid containing only the polymer (no soap present) showed a wear scar diameter of 1.5 mm. after the one hour test. This is considered excessive wear.
- Example II The same product containing 1% of sodium soap of C Oxo acid (Example I) showed a wear scar diameter of only 0.54 mm. which is fully equivalent to results obtained with mineral oils.
- the product of Example II showed only slightly higher wear, 0.67 mm. scar diameter.
- the blends containing the soaps also prevented rusting of steel specimens stored in the fluids for periods up to a month.
- Example I 0. 54 N 0 Rust.
- Example II 0. 67 N 0 Rust. Fluid Without Soap 1. 50 Heavy Rust in less than 24 hours.
- the quantity of soap which may be used may varywill depend upon its type, but in general about to of a polyglycol ether type thickener is preferred. These are highly suitable because of their excellent compatibility with the glycols. In some cases as little as 5% up to as much as 40% of the-thickener may be employed.
- a preferred thickener is the material mentioned above with a viscosity of about 90,000 S.U.S. at 100 F.
- polymeric glycol ether products with S.U.S. viscosities substantially lower than 90,000, e.g., 400 and up to as much as 200,000 S.U.S. at 100 'F. may also be '1 used.
- Some of the commercial products in this class in- I alkali metal soap is a sodium soap.
- a composition consisting essentially of about 40 to 65% by Weight of water, about 9 to 34% by weight of ethylene glycol, about 20 to 30% by weight of a polyalkylene glycol having a viscosity at of between thus obtained.
- composition according to claim 1 wherein said polyalkylene glycol has a viscosity at 100 'F. of about 90,000 S.U.S.
- composition according to claim 2 wherein said 4.
- a composition according to claim 2 wherein said branched chain acid contains 13 carbon atoms.
- composition according to claim 2 wherein said branched chain acid contains 9 carbon atoms.
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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
United 1 NON-INFLAMMABLE HYDRAULIC FLUID Jones I. Wasson, Union, and Arnold J. Morway, Clark,
NJ assignors toEsso Research and Engineering Company, a corporation of Delaware No Drawing. Filed Sept. 14, 1955, Ser. No. 534,386 5 Claims. (Cl. 252-76) proposed. Some of these are of the hydrocarbon type which are advantageous for many applications but which are rather highly inflammable and unsuitable for certain uses. In industrial operation, such as the die casting of metals, for example, the control of the heavy casting machineryare operated largely by hydraulic means. The hydraulic fluids used in such controls have frequently been a source of fire and danger. For this reason there is a growing demand for noninflammable, hydraulic fluids. Glycolwater base'type fluids have been investigated to a considerable extent for this application. These fluids are not absolutely noninflammable but their resistance 'to flame is so much "greater than that of the hydrocarbon oils that they may be considered substantially noninflammable.
,On the other hand, although the flame resistant prop with the glycol-water base. Unless the thickener is compatible, the solution is unstable, the thickener tending to settle out and to interfere with proper operation of the Y fluid or the mechanism in which his used.
Furthermore,j as suggested above, water base hydraulic fluids have relatively very poor lubricating characteristics.
While hydraulic fluids are used primarily to'transmit forces through hydraulic means, they must provide lubrication for hydraulic pumps and associated mechanical parts in order topre'ventexcessive wear. The prior art hydraulic fluids of this type have been poor lubricants, on the whole. Many of them have permitted rusting of ferrous metalswhich obviously is highly objectionable. Aside from the damage done by the rust itself, the parts frequently stick, or freeze, 'so. that the operation is uncertain [and erratic; In vital hydraulic controls, such erratic o'perat ion'cannot be'tolerated at all and it is alwaysobjectionable in any'hydraulic mechanism.
It is known that certain of the long chain fatty acids and derivatives thereof have useful anti-wear and rust preventive properties when used in hydrocarbon base oils. Thus, the use of oleic acid, stearic acid, lauric acid, the
" tent Patented Aug. 2, 1960 2 corresponding fatty oils or glycerides and the like, in mineral base oils to reduce wear and also to help inhibit rust is well known. These materials, however, are sub stantially insoluble in water base hydraulic oils or fluids and are, therefore, unsuitable for use in the compositions of the present invention.
According to the present invention it has been discovered that a combination of glycol-water base fluid may be blended with a polyglycol or polyglycolether type polymeric thickener to improve viscosity and viscosity index, and a water soluble soap of an organic aliphatic acid may be used to impart the other required properties. In particular a water soluble soap, preferably an alkali metal soap of a moderately long chain aliphatic acid, shows exceptional utility as an anti-wear and anti-rust agent.
The alkali metal soaps of straight chain fatty acids of C chain length or longer are substantially insoluble in Water. The branched chain soaps, however, of acids having from at least 7 carbon atoms up to about 14 carbon atoms are soluble in water, and soaps of highly branched acids up to about C are soluble in the composi tions of this invention. They may be used to form stable blends having good wear preventing properties,
5 branched chain acids and are obtained by subjecting vated temperatures and pressures. Operable catalysts include the Well known cobalt containing catalysts, for example, cobalt, stearate, cobalt carbonyl, and the like. Pressures ranging from about 100 to about 300 atmospheres are used and a temperature in the rangeof about 200 to about 400 F. The ratio of hydrogen to carbon monoxide employed may vary betweenabout 0.5 volume to 2.0, volumes of hydrogen 'per volume of carbon monoxide. i
The olefinic starting material preferably comprises olefins having frorn 8 to 12 carbon atoms per molecule,
however, olefins having from 6 to; 24 carbon atoms may 1 be used. The olefin is carbonylated in the process and r the resulting aldehyde hasone more carbon atom the starting olefin. The process proceeds in accordance with the following equatiom 7 r V 7 RCH=CH2+CO+HZWRCHPCHFCHO V a Ron-on.
one The aldehyde resulting from the carbonylat-ion of the olefin is .then oxidized to obtain the desired branched chain acid. This reaction is brought about by subjecting the aldehyde in basic solution to the action of an oxygenating substance suchiasa; mixture ofnitrogen and oxygen (a irj)',. a material. releasing Enasc ent oxygen (KMnQ or thelike; 'Theoxidation reaction, one which is well known in the art, proceeds in accordance with the following equation:
i RCHz-CHz-CHO+[O1wROHr-CHr-(F-OH If desired, the Oxo reaction may be carried out in the presence of water in the form of vapor instead of hydrogen. The desired branched chain acid is thus ob tained directly from the x0 process. The same conditions of temperature and pressure are necessary for this reaction as for the carbonylation reaction resulting in the aldehyde as described above.
Regardless of the manner of preparing the acid for the concept of this invention it is essential only that material be a branched chain acid and that it contain from 9 to 13 carbon atoms. 7 V Y The soaps of these branched chain acids are prepared by reaction of the acid with the desired alkali metal hydroxide. Especially preferred are the sodium or potassium soaps which have excellent water solubility and thus provide clear stable solutions.
' A preferred composition consists of about 40 to 65% by weight of water, about 9 to 34% of ethylene glycol, 20 to 30% of a polyglycol or polyglycolether thickener of sufficiently high molecular weight to increase the viscosity substantially, and 0.5 to 2% of the sodium soap of Oxo or other branched chain acids of the C to C range. The potassium soaps may be substituted for the sodium soaps and the proportion of water to ethylene glycol may be varied considerably depending upon the viscosity, pour point, freezing point, or other requirements.
EXAMPLE I A fluid containing 62.9% by weight of water, 11.1% of ethylene glycol, 25% of a polymeric glycolether having a viscosity of about 90,000 S.U.S. at 100 F., sold by Union Carbide and Carbon Chemical Corp., under the trade name Ucon 75 H-90,000 1 was modified by addition of 1% of the sodium soap of a C 0x0 acid. This product had a viscosity of 290 S.U.S. at 100 F. and a viscosity index of 162.
EXAMPLE II A composition was prepared exactly as above except that 1% of sodium soap of 0,, 0x0 acid was used as the modifier. Comparative lubrication tests were made using the 4-ball wear tester wherein three ball bearings, onehalf inch in diameter, are clamped in a holding device and a fourth ball is rotated so as to bear on the first three under an applied load. This test of steel on steel was conducted at 167 F. under a 10 kg. load for one hour. In this test a glycol water base fluid containing only the polymer (no soap present) showed a wear scar diameter of 1.5 mm. after the one hour test. This is considered excessive wear. The same product containing 1% of sodium soap of C Oxo acid (Example I) showed a wear scar diameter of only 0.54 mm. which is fully equivalent to results obtained with mineral oils. The product of Example II showed only slightly higher wear, 0.67 mm. scar diameter. The blends containing the soaps also prevented rusting of steel specimens stored in the fluids for periods up to a month.
From the foregoing it is evident that the soaps are highly eifective for imparting anti-wear and anti-rust properties to the blends. Results are tabulated as follows:
A commercially available polyalkylene glycol prepared by Table I Wear Scar, Rust Test Fluid mm. in 4- Result Ball Test;
Example I 0. 54 N 0 Rust. Example II 0. 67 N 0 Rust. Fluid Without Soap 1. 50 Heavy Rust in less than 24 hours.
The quantity of soap which may be used may varywill depend upon its type, but in general about to of a polyglycol ether type thickener is preferred. These are highly suitable because of their excellent compatibility with the glycols. In some cases as little as 5% up to as much as 40% of the-thickener may be employed. A preferred thickener is the material mentioned above with a viscosity of about 90,000 S.U.S. at 100 F. However, polymeric glycol ether products with S.U.S. viscosities substantially lower than 90,000, e.g., 400 and up to as much as 200,000 S.U.S. at 100 'F., may also be '1 used. Some of the commercial products in this class in- I alkali metal soap is a sodium soap.
clude Ucon H-490, Ucon 75 H-1400, and Ucon 75 H-9150 sold by the Carbide and Carbon Chemical Corp.
. It will be understood that additional conventional modifiers such as rust inhibitors, anti-foaming agents and the i for the same inventors.
What is claimed is:
1. A composition consisting essentially of about 40 to 65% by Weight of water, about 9 to 34% by weight of ethylene glycol, about 20 to 30% by weight of a polyalkylene glycol having a viscosity at of between thus obtained.
2. A composition according to claim 1 wherein said polyalkylene glycol has a viscosity at 100 'F. of about 90,000 S.U.S.
3. A composition according to claim 2 wherein said 4. A composition according to claim 2 wherein said branched chain acid contains 13 carbon atoms.
5. A composition according to claim 2 wherein said branched chain acid contains 9 carbon atoms.
References Cited in the file of this patent UNITED STATES PATENTS 1,928,956 Tatter Oct. 3, 1933 2,553,364 Fasce May 15, 1951 2,558,030 Zisman June 26, 1951 2,602,780 Zisman et a1. July 8, 1952 2,737,497 Wasson et a1. Mar. 6, 1956 2,768,141 Langer Oct. 23, 1956
Claims (1)
1. A COMPOSITION CONSISTING ESSENTIALLY OF ABOUT 40 TO 65% BY WEIGHT OF WATER, ABOUT 9 TO 34% BY WEIGHT OF ETHYLENE GLYCOL, ABOUT 20 TO 30% BY WEIGHT OF A POLYALKYLENE GLYCOL HAVING A VISCOSITY OF 100*F. OF BETWEEN 400 AND 200,000 S.U.S AND 0.5 TO 2.0% BY WEIGHT OF AN ALKALI METAL SOAP OF A BRANCHED CHAIN ACID CONTAINING FROM 9 TO 13 CARBON ATOMS, SAID ACID BEING PREPARED BY THE CARBONYLATION OF AN OLEFINIC HYDROCARBON HAVING FROM 8 TO 12 CARBON ATOMS WITH CARBON MONOXIDE AND HYDROGEN IN THE PRESENCE OF A COBALT CARBONYLATION CATALYST AT A TEMPERATURE OF ABOUT 200 TO ABOUT 400*F. AND AT A PRESSURE OF ABOUT 100 TO ABOUT 300 ATMOSPHERES AND THE SUBSEQUENT OXIDATION OF THE CARBONYLATED OLEFINS THUS OBTAINED.
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US534386A US2947699A (en) | 1955-09-14 | 1955-09-14 | Non-inflammable hydraulic fluid |
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US534386A US2947699A (en) | 1955-09-14 | 1955-09-14 | Non-inflammable hydraulic fluid |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
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US3108076A (en) * | 1960-07-27 | 1963-10-22 | Gen Motors Corp | Hydraulic pressure transmission fluid |
US3206486A (en) * | 1962-06-15 | 1965-09-14 | Dow Chemical Co | Polyglycol esters of olefinically unsaturated higher fatty acids |
US3330764A (en) * | 1962-06-15 | 1967-07-11 | Dow Chemical Co | Polyglycol esters |
US3331779A (en) * | 1963-12-30 | 1967-07-18 | Douglas Aircraft Co Inc | Inhibition of corrosion of hydraulic fluids |
US3352783A (en) * | 1963-12-30 | 1967-11-14 | Mc Donnell Douglas Corp | Hydraulic fluid |
US3371046A (en) * | 1963-12-30 | 1968-02-27 | Douglas Aircraft Co Inc | Inhibition of corrosion of hydraulic fluids |
US3379644A (en) * | 1966-03-16 | 1968-04-23 | Gen Aniline & Film Corp | Hydraulic fluid compositions |
US3533952A (en) * | 1965-08-11 | 1970-10-13 | Western Co Of North America | Transmission of mechanical power |
US4414125A (en) * | 1979-12-01 | 1983-11-08 | Chemische Werke Huels Aktiengesellschaft | Alkali metal or amine salts of a mixture of 2- and 3-alkyladipic acids as corrosion inhibitors |
US4855070A (en) * | 1986-12-30 | 1989-08-08 | Union Carbide Corporation | Energy transmitting fluid |
WO1996034076A1 (en) * | 1995-04-25 | 1996-10-31 | Houghton Vaughan Plc | Water-based hydraulic fluid composition |
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US1928956A (en) * | 1930-03-22 | 1933-10-03 | Lewis Differential Company | Brake fluid composition |
US2553364A (en) * | 1948-06-24 | 1951-05-15 | Standard Oil Dev Co | Oxidation process to form free fatty acids |
US2558030A (en) * | 1948-09-23 | 1951-06-26 | William A Zisman | Noninflammable hydraulic fluids and lubricants |
US2602780A (en) * | 1945-08-17 | 1952-07-08 | William A Zisman | Hydraulic fluid |
US2737497A (en) * | 1952-01-02 | 1956-03-06 | Exxon Research Engineering Co | Non-inflammable hydraulic fluid |
US2768141A (en) * | 1952-10-24 | 1956-10-23 | Union Carbide & Carbon Corp | Noninflammable hydraulic fluids |
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Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1928956A (en) * | 1930-03-22 | 1933-10-03 | Lewis Differential Company | Brake fluid composition |
US2602780A (en) * | 1945-08-17 | 1952-07-08 | William A Zisman | Hydraulic fluid |
US2553364A (en) * | 1948-06-24 | 1951-05-15 | Standard Oil Dev Co | Oxidation process to form free fatty acids |
US2558030A (en) * | 1948-09-23 | 1951-06-26 | William A Zisman | Noninflammable hydraulic fluids and lubricants |
US2737497A (en) * | 1952-01-02 | 1956-03-06 | Exxon Research Engineering Co | Non-inflammable hydraulic fluid |
US2768141A (en) * | 1952-10-24 | 1956-10-23 | Union Carbide & Carbon Corp | Noninflammable hydraulic fluids |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3108076A (en) * | 1960-07-27 | 1963-10-22 | Gen Motors Corp | Hydraulic pressure transmission fluid |
US3206486A (en) * | 1962-06-15 | 1965-09-14 | Dow Chemical Co | Polyglycol esters of olefinically unsaturated higher fatty acids |
US3330764A (en) * | 1962-06-15 | 1967-07-11 | Dow Chemical Co | Polyglycol esters |
US3331779A (en) * | 1963-12-30 | 1967-07-18 | Douglas Aircraft Co Inc | Inhibition of corrosion of hydraulic fluids |
US3352783A (en) * | 1963-12-30 | 1967-11-14 | Mc Donnell Douglas Corp | Hydraulic fluid |
US3371046A (en) * | 1963-12-30 | 1968-02-27 | Douglas Aircraft Co Inc | Inhibition of corrosion of hydraulic fluids |
US3533952A (en) * | 1965-08-11 | 1970-10-13 | Western Co Of North America | Transmission of mechanical power |
US3379644A (en) * | 1966-03-16 | 1968-04-23 | Gen Aniline & Film Corp | Hydraulic fluid compositions |
US4414125A (en) * | 1979-12-01 | 1983-11-08 | Chemische Werke Huels Aktiengesellschaft | Alkali metal or amine salts of a mixture of 2- and 3-alkyladipic acids as corrosion inhibitors |
US4855070A (en) * | 1986-12-30 | 1989-08-08 | Union Carbide Corporation | Energy transmitting fluid |
WO1996034076A1 (en) * | 1995-04-25 | 1996-10-31 | Houghton Vaughan Plc | Water-based hydraulic fluid composition |
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