US3814691A - Alkyl(polyalkoxy)silanes as components in hydraulic fluids - Google Patents
Alkyl(polyalkoxy)silanes as components in hydraulic fluids Download PDFInfo
- Publication number
- US3814691A US3814691A US00259894A US25989472A US3814691A US 3814691 A US3814691 A US 3814691A US 00259894 A US00259894 A US 00259894A US 25989472 A US25989472 A US 25989472A US 3814691 A US3814691 A US 3814691A
- Authority
- US
- United States
- Prior art keywords
- carbon atoms
- alkyl
- weight
- hydraulic
- percent
- 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
Links
- 239000012530 fluid Substances 0.000 title abstract description 58
- 125000000217 alkyl group Chemical group 0.000 title description 34
- 150000004756 silanes Chemical class 0.000 title description 5
- 239000000203 mixture Substances 0.000 abstract description 42
- 150000001642 boronic acid derivatives Chemical class 0.000 abstract description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 description 44
- 239000002585 base Substances 0.000 description 25
- 150000001282 organosilanes Chemical class 0.000 description 23
- 239000000306 component Substances 0.000 description 21
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 20
- 238000009835 boiling Methods 0.000 description 17
- 239000003112 inhibitor Substances 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 229910052739 hydrogen Inorganic materials 0.000 description 16
- 239000001257 hydrogen Substances 0.000 description 16
- 239000000654 additive Substances 0.000 description 15
- 125000002947 alkylene group Chemical group 0.000 description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 11
- -1 borate ester Chemical class 0.000 description 11
- 239000003085 diluting agent Substances 0.000 description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- 239000003963 antioxidant agent Substances 0.000 description 10
- 230000007797 corrosion Effects 0.000 description 10
- 238000005260 corrosion Methods 0.000 description 10
- 238000010992 reflux Methods 0.000 description 10
- 230000003078 antioxidant effect Effects 0.000 description 7
- 230000005540 biological transmission Effects 0.000 description 7
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- 125000005702 oxyalkylene group Chemical group 0.000 description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 3
- 101150065749 Churc1 gene Proteins 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 102100038239 Protein Churchill Human genes 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- ZFAKTZXUUNBLEB-UHFFFAOYSA-N dicyclohexylazanium;nitrite Chemical compound [O-]N=O.C1CCCCC1[NH2+]C1CCCCC1 ZFAKTZXUUNBLEB-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000006353 oxyethylene group Chemical group 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-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
- UQRONKZLYKUEMO-UHFFFAOYSA-N 4-methyl-1-(2,4,6-trimethylphenyl)pent-4-en-2-one Chemical group CC(=C)CC(=O)Cc1c(C)cc(C)cc1C UQRONKZLYKUEMO-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 101100277337 Arabidopsis thaliana DDM1 gene Proteins 0.000 description 1
- MYPKNOIDGYUDRC-UHFFFAOYSA-N CCCCNCCCC.CCCCNCCCC.CCCCNCCCC.OB(O)O Chemical class CCCCNCCCC.CCCCNCCCC.CCCCNCCCC.OB(O)O MYPKNOIDGYUDRC-UHFFFAOYSA-N 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241001620634 Roger Species 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- FZQSLXQPHPOTHG-UHFFFAOYSA-N [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 Chemical compound [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 FZQSLXQPHPOTHG-UHFFFAOYSA-N 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 101150113676 chr1 gene Proteins 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- TUEYHEWXYWCDHA-UHFFFAOYSA-N ethyl 5-methylthiadiazole-4-carboxylate Chemical compound CCOC(=O)C=1N=NSC=1C TUEYHEWXYWCDHA-UHFFFAOYSA-N 0.000 description 1
- 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 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229940096992 potassium oleate Drugs 0.000 description 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N60/00—Superconducting devices
-
- 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/082—Inorganic acids or salts thereof containing nitrogen
- C10M2201/083—Inorganic acids or salts thereof containing nitrogen nitrites
-
- 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
- C10M2201/087—Boron oxides, acids or salts
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
-
- 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
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
-
- 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
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/024—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/18—Tall oil 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
- C10M2207/20—Rosin 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
- 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
- C10M2215/02—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
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
-
- 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
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/062—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups bound to the aromatic ring
-
- 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
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
- C10M2215/065—Phenyl-Naphthyl 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
-
- 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
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/221—Six-membered rings containing nitrogen and carbon 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
-
- 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
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
- C10M2215/226—Morpholines
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/30—Heterocyclic compounds
-
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/108—Phenothiazine
-
- 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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/04—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having a silicon-to-carbon bond, e.g. organo-silanes
-
- 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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
-
- 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
- C10N2040/06—Instruments or other precision apparatus, e.g. damping 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
Definitions
- the hydraulic fluid of this invention may contain a base component made up of a mixture of selected alkyl (polyalkoxy) silanes, as defined above, and selected borate esters.
- This invention relates to water-insensitive hydraulic fluids which employ selected alkyl (polyalkoxy) silanes as the base stock or lubricant.
- the new and improved water-insensitive hydraulic fluids of this invention are useful as hydraulic pressure transmission fluids in a variety of hydraulic systems such as hydraulic brake systems, hydraulic steering mechanisms, hydraulic transmissions, hydraulic jacks, and hydraulic lifts.
- the hydraulic fluids of this invention which contain selected alkyl (polyalkoxy) silanes, hereinafter referred to as organosilanes, as the base fluid, possess a high boiling point, have a high degree of compatability with other fluids, have desired viscosity and corrosion properties, have a high degree of water tolerance and are of low cost.
- organosilanes as the base fluid
- These fluids are particularly advantageous in environments which are exposed to water or water vapor such as brake fluids used in automotive brake systems.
- the effect of water on hydraulic brake fluids has been studied extensively and it is now recognized and agreed that the presence of water has a dramatic effect on lowering of the boiling point (see Automotive Hydraulic Brake Fuilds by C. F.
- hydraulic pressure transmission fluids are made up of three principal units.
- the first is a base or lubricant for the system which may include heavy body fluids such as polyglycols, castor oil, mixtures of these materials etc.
- the second basic unit is made up of diluents and other additives which modify the physical properties of the base fluid such as the viscosity.
- the third basic unit is represented by an inhibitor system comprising small quantities of inhibitors or addtives which are added to modify the chemical properties of the base fluid.
- Such inhibitors include antioxidants, anticorrosion agents and additives to improve wetting and flow properties.
- organosilanes used as the base component in the hydraulic fluids of this invention have the following general formula:
- R is an alkyl group of 1 to 10 carbon atoms such as methyl, ethyl, butyl, isobutyl, octyl, nonyl, and decyl or an aryl group of 6 to 10 carbon atoms such as phenyl, tolyl, xylyl, mesityl and naphthyl;
- R is an alkyl group of l to 4 carbon atoms such as methyl, ethyl and butyl;
- R" is alkylene of 2 to 4 carbon atoms;
- y is an integer of 1 to 5 and z is an integer of 1 to 3.
- the R, R and R" groups may include branched or straight chained derivatives and it is also intended that the alkylene oxide group (O-R") in the above formula (:I) include mixtures of said alkylene oxides.
- organosilanes of the above formula include for example:
- Organosilanes of the above type (I) can conveniently be prepared for example, by reacting an alkyl-halo-silane with polyalkylene glycol monoalkyl or monoaryl others in an inert medium.
- organosilanes as described above are readily available by the same technique. Further disclosure for the preparation of organosilanes of this type may be found in The Preparation of Alkoxysilanes from Glycols and Glycol Monoethers by H. G. Emblem and K. Hargreaves in J. of Inorganic Nuclear Chemistry, vol. 30, 1968, pp. 721-727 and Organosilicon Compounds by C. Eaborn, 1960, New York Academic Press. Inc., pp. 288-297.
- the hydraulic fluids of this invention which have the organosilanes (I) as the base or lubricant component, may additionally include as part of such base component, varying amounts of the borate esters of the type disclosed in application Ser. No. 717,996, now US. Pat. 3,625,899 and the bis-borate and bridged-borate esters of the type disclosed in application Ser. No. 717,997, now abandoned, both applications of A. Sawyer and D. Csejka and filed Apr. 1, 1968.
- the complete disclosure of the aforementioned applications which define the particular borate esters and their method of preparation are incorporated herein by reference.
- borate esters disclosed in application Ser. No. 717,- 996 generally consist of the following formulas:
- R is an alkyl of from 1 to 4 carbon atoms
- x is an integer of from 2 to 4
- y is an integer of from 2 to 4.
- R is alkyl of from 1 to 4 carbon atoms
- R and R are independently selected from the group consisting of hydrogen and methyl
- m and n are positive integers whose sum is from 2 to 20, and with the proviso that one of R and R is methyl and one of R and R is hydrogen.
- R is alkyl of from 1 to 4 carbon atoms, R, is a heteric oxyalkylene chain of the formula:
- T T and T are each an independently selected alkyl group having from 1 to 4 carbon atoms; R R R R R and R are independently selected from the group consisting of hydrogen and methyl, n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to 20, and with the proviso that in no more than two of the chains is the sum of n and m the same.
- R3 [(OCHzCHRrM-(OCHaCHRzhOL 3.. RAKOCHQCHR1) (OCHQCHR )nO ⁇ [O(RflCHCHlO)n-(R1CHCHgO)m]RO
- R and R are independently selected from the group consisting of hydrogen and methyl
- R R R and R are each an independently selected alkyl group having from 1 to 4 carbon atoms and n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to 20
- R1 [(O CHzCHRthr-(O CH CHRDuOk B0R.
- R and R are independently selected from the group consisting of hydrogen or methyl
- R and R are each an independently selected alkyl group having from 1 to 4 carbon atoms
- R is the organic residue exclusive of reactive hydroxyl groups of a polyol
- p is an integer of from 2 to 6 inclusive
- n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to 20.
- borate esters include, for example: s( 2 2) 2 a a 'i a z) 4 a' [CH OCH CH )'(OCH CHCH O] ;;-B,
- the borate esters are admixed with the organosilanes forming the base component of the hydraulic fluid of this invention, widely varying proportions of the organosilanes and borate esters may be used. More particularly, the base component may contain an organosilane and from 0 to 95% by weight of borate ester and preferably from 25 to by weight.
- the amount of base component which is used in the hydraulic fluid of this invention can vary widely. Generally the base component will constitute at least about 20 percent by weight of the fluid and preferably at least about 40 percent by weight based on the total weight of the fluid composition.
- the organosilane containing base component may consist of one or more glycol monoethers or diethers of the formula:
- R is alkyl of 1 to 4 carbon atoms
- R is alkylene of 2 to 4 carbon atoms
- R is hydrogen or alkyl of from 1 to 4 carbon atoms
- y is an integer of from 2 to 4.
- the R, R and R groups may be straight chained or branched and the alkylene oxide group (O-R,,) in the above formula may include mixtures of said alkylene oxides.
- one or more glycols such as the alkylene glycols having for example, the following formula may be used:
- R is alkylene of from 2 to 3 carbon atoms and z is an integer of from 1 to 5.
- Illustrative of the above-described diluents are the fol lowing: diethylene glycol monoethyl ether, diethylene glycol-monobutyl ether, triethylene glycol monomethyl ether, triethylene glycol monoethyl ether, tetraethylene glycol monomethyl ether, ethylene glycol, propylene glycol, diethylene glycol and tetraethylene glycol.
- Various other diluents and mixtures thereof, which are well known in the art may also be used with the organosilane containing base component of this invention.
- US. Pat. 3,377,288 and 5 applications 717,996 and 717,997 previously noted, disclose various diluents which may be utilized.
- the particular amount of diluents which is used is not critical and widely varying amounts may be used. More particularly, the diluent components may constitute from up to about 80 percent by weight of the fluid and preferably from about 20 to about 60 percent.
- additives may be added to the hydraulic fluids of this invention containing the organosilane base component-to control or modify various chemical and physical properties.
- various types of additives which can be added to the hydraulic fluids of this invention are included inhibitors for pH and corrosion control, antioxidants, rust inhibitors, viscosity index improvers, pour point depressants, lubricating additives, antifoamants, stabilizers, vapor phase corrosion inhibitors, rubber swelling adjusters, demulsifiers, dyes and odor suppressants.
- the total amount of additives which may be incorporated into the fluid composition will vary between about 0.01 to about 20 percent, preferably from about 0.1 to 8 percent and more preferably from about 0.2 to about percent by weight, based on the total weight of the hydraulic fluid composition.
- alkaline inhibitors for pH and corrosion control can be employed in an amount sufficient to maintain alkaline conditions in the fluid compositions, e.g. at a pH value of from about 7.0 to about 11.5 if desired.
- These inhibitors are generally added in an amount of from about 0.01 to about 8.0 percent by weight based on the total weight of fluid composition and preferably from about 0.5 to about 6.0 percent.
- alkaline inhibitors include for example: alkali metal borates such as sodium borate and potassium tetraborate, alkali metal salts of higher fatty acids such as potassium oleate, the potassium soap of rosin or tall oil fatty acids, amines such as morpholine and ethanolamine and amine salts such as monoor dibutyl ammonium borates.
- antioxidants include, 2,2-di-(4-hydroxypheny1)propane, phenothiazine, amines such as phenyl-alpha-naphthylamine and hindered phenols such as dibutyl cresol.
- the amount of antioxidant used will vary from 0 to about 3 percent by weight and preferably from about 0.001 to about 2 percent by weight based on the total weight of the fluid composition.
- additives may be incorporated into the fluid composition.
- corrosion inhibitors such as butynediol and rubber swelling adjusters such as dodecyl benzene may be used.
- inhibitors and additives are merely exemplary and are not intended as an exclusive listing of the many well-known materials which can be added to fluid compositions to obtain various desired properties.
- Other illustrations of additives and diluents which may be used can be found in US. Pat. 3,377,288 and copending applications 717,996 and 717,997 previously noted and in Introduction to Hydraulic Fluids by Roger -E. Hatton, Reinhold Publishing Corp. (1962).
- a hydraulic fluid composition consisting essentially of:
- R is selected from the group consisting of alkyl of 1 to 10 carbon atoms and an aryl group of 6 to 10 carbon atoms, R is an alkyl group of 1 to 4 carbon atoms, R" is alkylene of from 2 to 4 carbon atoms, y is an integer of 1 to 5 and z is an integer of 1 to 3 (b) from 0 to about percent by weight, based on the total weight of the hydraulic fluid composition, of at least one diluent selected from the group consisting of:
- R is alkyl of 1 to 4 carbon atoms
- R is alkylene of 2 to 4 carbon atoms
- R is selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms and y is an integer of 2 to 4, and
- R is alkylene of from 2 to 3 carbon atoms and z is an integer of from 1 to 5 and (c) from about 0.01 to about 20 percent by weight,
- an additive which is an alkaline inhibitor for pH and corrosion control.
- composition of claim 1 which contains from about 0.01 to about 8.0 percent by weight of said alkaline inhibitor for pH and corrosion control.
- composition of claim 1 which contains at least about 40 percent by weight of said organosilane base component.
- composition of claim 3 which contains from about 20 to about 60 percent by weight of said diluent.
- composition of claim 1 wherein said additive is an antioxidant.
- composition of claim 1 wherein said additive is a rubber swelling adjuster.
- composition of claim 1 wherein said alkaline inhibitor is used in an amount of from about 0.5 to about 6.0% by weight, based on the total weight of the hydraulic fluid composition.
- composition of claim 1 wherein said additive is a mixture of an alkaline inhibitor for pH and corrosion control and an antioxidant.
- composition of claim 9 wherein in said organosilane R is methyl and R methyl.
- composition of claim 10 wherein in said organosilane -R" contains two carbon atoms, y is 3 and z is 2.
- composition of claim 14 wherein the base component contains from about 0 to about percent by weight, based on the total Weight of base component, of at leagt one borate ester selected from the group consistmg 0 wherein R is an alkyl of from 1 to 4 carbon atoms, x is an integer of from 2 to 4 and y is an integer of from 2 to 4,
- R is alkyl of from 1 to 4 carbon atoms
- R and R are independently selected from the group consisting of hydrogen and methyl
- m and n are positive integers whose sum is from 2 to 20, and with the proviso that one of R and R is methyl and one of R and R is hydrogen
- R is alkyl of from 1 to 4 carbon atoms
- Rg is a heteric oxyalkylene chain of the formula:
- R and R are independently selected from the group consisting of hydrogen and methyl;
- R R R and R are each an independently selected alkyl group having from 1 to 4 carbon atoms and n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to and
- R and R are each an independently selected alkyl group having from 1 to 4 carbon atoms;
- R is the organic residue exclusive of reactive hydroxyl groups of a polyol, p is an integer of from 2 to 6 inclusive and n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to 20.
- composition of claim 14 wherein said additive is an antioxidant.
- composition of claim 14 wherein said organosilane has the formula:
- composition of claim 14 wherein said organosilane has the formula:
- R is selected from the group consisting of alkyl of 1 to 10 carbon atoms and aryl of 6 to 10 carbon atoms, R is an alkyl group of 1 to 4 carbon atoms, R is alkylene of from 2 to 4 carbon atoms, y is an integer of 1 to 5 and z is an integer of 1 to 3.
- the base component contains from 0 to about percent by weight, based on the total weight of base component, of at least one borate ester selected from the group consisting of:
- R is an alkyl of from 1 to 4 carbon atoms
- x is an integer of from 2 to 4
- y is an integer of from 2 to 4 wherein R is alkyl of from 1 to 4 carbon atoms
- R and R are independently selected from the group consisting of hydrogen and methyl
- m and n are positive integers whose sum is from 2 to 20, and with the proviso that one of R and R is methyl and one of R and ⁇ R is hydrogen wherein R is alkyl of from 1 to 4 carbon atoms
- Rg is a heteric oxyalkylene chain of the formula:
- said hydraulic FOREIGN PATENTS pressure transmission fluid contains from about 0.01 to about 20% by weight, based on the total weight of the 960240 6/1964 England 2604483 hydraulic fluid compositions of an antioxidant.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
A HYDRAULIC FLUID CONTAINING AS THE BASE COMPONENT AT LEAST ONE ALKYL (POLYALKOXY) SILANE OF THE FORMULA:
(R(O-R'''')YO)ZSIR''4-Z
WHEREIN R IS AN ALKYL GROUP OF 1 TO 10 CARBON ATOMS OR AN ARYL GROUP OF 6 TO 10 CARBON ATOMS; R'' IS AN ALKYL GROUP OF 1 TO 4 CARBON ATOMS, R'''' IS ALKYLENE OF FROM 2 TO 4 CARBON ATOMS, Y IS AN INTEGER OF 1 TO 5 AND Z IS AN INTEGER OF 1 TO 3. ADDITIONALLY, THE HYDRAULIC FLUID OF THIS INVENTION MAY CONTAIN A BASE COMPONENT MADE UP OF A MIXTURE OF SELECTEE ALKYL (POLYALKOXY) SILANES, AS DEFINED ABOVE, AND SELECTED BORATE ESTERS.
(R(O-R'''')YO)ZSIR''4-Z
WHEREIN R IS AN ALKYL GROUP OF 1 TO 10 CARBON ATOMS OR AN ARYL GROUP OF 6 TO 10 CARBON ATOMS; R'' IS AN ALKYL GROUP OF 1 TO 4 CARBON ATOMS, R'''' IS ALKYLENE OF FROM 2 TO 4 CARBON ATOMS, Y IS AN INTEGER OF 1 TO 5 AND Z IS AN INTEGER OF 1 TO 3. ADDITIONALLY, THE HYDRAULIC FLUID OF THIS INVENTION MAY CONTAIN A BASE COMPONENT MADE UP OF A MIXTURE OF SELECTEE ALKYL (POLYALKOXY) SILANES, AS DEFINED ABOVE, AND SELECTED BORATE ESTERS.
Description
United States Patent ()flice' 3,814,691 Patented June 4, 1974 3,814,691 ALKYL (POLYALKOXY) SILANES AS COM- PONENTS IN HYDRAULIC FLUIDS David A. Csejka, Orange, and Henry F. Lederle, North Haven, 'Conn., assignors to Olin Corporation No Drawing. Continuation-impart of abandoned application Ser. No. 75,719, Sept. 25, 1970. This application June 5, 1972, Ser. No. 259,894
Int. Cl. C09k 3/00 US. Cl. 252-78 21 Claims ABSTRACT OF THE DISCLOSURE A hydraulic fluid containing as the base component at least one alkyl (polyalkoxy) silane of the formula:
wherein R is an alkyl group of l to 10 carbon atoms or an aryl group of 6 to 10 carbon atoms, R is an alkyl group of 1 to 4 carbon atoms, R" is alkylene of from 2 to 4 carbon atoms, y is an integer of 1 to 5 and z is an integer of l to 3. Additionally, the hydraulic fluid of this invention may contain a base component made up of a mixture of selected alkyl (polyalkoxy) silanes, as defined above, and selected borate esters.
This application is a continuation-in-part of co-pending application Ser. No. 75,719 filed Sept. 25, 1970 and now abandoned.
This invention relates to water-insensitive hydraulic fluids which employ selected alkyl (polyalkoxy) silanes as the base stock or lubricant.
The new and improved water-insensitive hydraulic fluids of this invention are useful as hydraulic pressure transmission fluids in a variety of hydraulic systems such as hydraulic brake systems, hydraulic steering mechanisms, hydraulic transmissions, hydraulic jacks, and hydraulic lifts.
A great number of hydraulic fluid compositions are known in the art as shown for example in Introduction to Hydraulic Fluids by Roger E. Hatton, Reinhold Publishing Corporation, 1962. Although the hydraulic fluids of the prior art possess one or more of the desired characteristics of viscosity-temperature relationship, volatility or pour-point, they generally have one or more disadvantages such as having low boiling points, not being water-insensitive and not being stable against oxidation, deterioration and corrosion.
Now it has been found that the hydraulic fluids of this invention which contain selected alkyl (polyalkoxy) silanes, hereinafter referred to as organosilanes, as the base fluid, possess a high boiling point, have a high degree of compatability with other fluids, have desired viscosity and corrosion properties, have a high degree of water tolerance and are of low cost. These fluids are particularly advantageous in environments which are exposed to water or water vapor such as brake fluids used in automotive brake systems. The effect of water on hydraulic brake fluids has been studied extensively and it is now recognized and agreed that the presence of water has a dramatic effect on lowering of the boiling point (see Automotive Hydraulic Brake Fuilds by C. F. Pickett published as part of the 51st Mid-Year Meeting Proceedings of the Chemical Specialties Manufacturing Association, Inc., 1965). A high boiling point of the brake fluid is necessary to prevent vapor lock which results in a loss of braking power thus frequently causing an accident. When 3.5 percent Water was added to a conventional brake fluid having an initial boiling point of 562 -F., the boiling point dropped to a level of about 280 F. In contrast when the same amount of water was added to several examples of the hydraulic fluids of this invention which contain an organosilane base component, the boilmg point did not drop as much and resulted in a desirably high wet boiling point of about 400 F. Thus it is apparent that the hydraulic fluids of this invention are distinctly superior to those of the art.
Generally, hydraulic pressure transmission fluids are made up of three principal units. The first is a base or lubricant for the system which may include heavy body fluids such as polyglycols, castor oil, mixtures of these materials etc. The second basic unit is made up of diluents and other additives which modify the physical properties of the base fluid such as the viscosity. Finally, the third basic unit is represented by an inhibitor system comprising small quantities of inhibitors or addtives which are added to modify the chemical properties of the base fluid. Such inhibitors include antioxidants, anticorrosion agents and additives to improve wetting and flow properties.
The organosilanes used as the base component in the hydraulic fluids of this invention have the following general formula:
wherein R is an alkyl group of 1 to 10 carbon atoms such as methyl, ethyl, butyl, isobutyl, octyl, nonyl, and decyl or an aryl group of 6 to 10 carbon atoms such as phenyl, tolyl, xylyl, mesityl and naphthyl; R is an alkyl group of l to 4 carbon atoms such as methyl, ethyl and butyl; R" is alkylene of 2 to 4 carbon atoms; y is an integer of 1 to 5 and z is an integer of 1 to 3. The R, R and R" groups may include branched or straight chained derivatives and it is also intended that the alkylene oxide group (O-R") in the above formula (:I) include mixtures of said alkylene oxides.
organosilanes of the above formula include for example:
Organosilanes of the above type (I) can conveniently be prepared for example, by reacting an alkyl-halo-silane with polyalkylene glycol monoalkyl or monoaryl others in an inert medium. Various other organosilanes as described above are readily available by the same technique. Further disclosure for the preparation of organosilanes of this type may be found in The Preparation of Alkoxysilanes from Glycols and Glycol Monoethers by H. G. Emblem and K. Hargreaves in J. of Inorganic Nuclear Chemistry, vol. 30, 1968, pp. 721-727 and Organosilicon Compounds by C. Eaborn, 1960, New York Academic Press. Inc., pp. 288-297.
The hydraulic fluids of this invention, which have the organosilanes (I) as the base or lubricant component, may additionally include as part of such base component, varying amounts of the borate esters of the type disclosed in application Ser. No. 717,996, now US. Pat. 3,625,899 and the bis-borate and bridged-borate esters of the type disclosed in application Ser. No. 717,997, now abandoned, both applications of A. Sawyer and D. Csejka and filed Apr. 1, 1968. The complete disclosure of the aforementioned applications which define the particular borate esters and their method of preparation are incorporated herein by reference.
The borate esters disclosed in application Ser. No. 717,- 996 generally consist of the following formulas:
wherein R is an alkyl of from 1 to 4 carbon atoms, x is an integer of from 2 to 4 and y is an integer of from 2 to 4.
(2) [R OCH CHR --(OCH CHR O] B wherein R is alkyl of from 1 to 4 carbon atoms, R and R are independently selected from the group consisting of hydrogen and methyl, m and n are positive integers whose sum is from 2 to 20, and with the proviso that one of R and R is methyl and one of R and R is hydrogen.
wherein R is alkyl of from 1 to 4 carbon atoms, R, is a heteric oxyalkylene chain of the formula:
wherein the sum of r and s is not more than 20 and wherein the weight percent of the oxyethylene units is not less than 20 based on the total Weight of all the oxyalkylene units, and
(4) O(RrOHCHaO)n(R5CHCH:0)mT1 B-O(RsCHCH )n(R- CHCHaO)mT:
0(RiCHCHiO)..(R,cHoH=0)mTi wherein T T and T are each an independently selected alkyl group having from 1 to 4 carbon atoms; R R R R R and R are independently selected from the group consisting of hydrogen and methyl, n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to 20, and with the proviso that in no more than two of the chains is the sum of n and m the same.
The bis-borate and bridge borate esters disclosed in application Ser. No. 717,997 generally consist of the following formulas:
(1) R3[(OCHzCHRrM-(OCHaCHRzhOL 3.. RAKOCHQCHR1) (OCHQCHR )nO{ [O(RflCHCHlO)n-(R1CHCHgO)m]RO wherein R and R are independently selected from the group consisting of hydrogen and methyl; R R R and R are each an independently selected alkyl group having from 1 to 4 carbon atoms and n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to 20; (2) R1[(O CHzCHRthr-(O CH CHRDuOk B0R. R [(0CH=CHR1)...(OCH2CHR,),.O] .L where R and R are independently selected from the group consisting of hydrogen or methyl; R and R are each an independently selected alkyl group having from 1 to 4 carbon atoms; R is the organic residue exclusive of reactive hydroxyl groups of a polyol, p is an integer of from 2 to 6 inclusive and n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to 20.
The above-noted borate esters include, for example: s( 2 2) 2 a a 'i a z) 4 a' [CH OCH CH )'(OCH CHCH O] ;;-B,
[C H (OCH CH OCH CHCH O] B,
' [c2H5(ocH2cHcH3)12-( H2 H2 8 13B.
3 z z) 2 z s) 41 3- c muocn cn (OCH CHCH ]0) 'B,
CIHIKO CHzCHCHs) i-(o CHQCHQQO] )0 (CHaCHQz-(CHaCHCHgOMCH;
Further examples of the above described borate esters and the methods for preparation are fully disclosed in the previously noted applications Ser. Nos. 717,996 and 717,- 997.
Generally when the borate esters are admixed with the organosilanes forming the base component of the hydraulic fluid of this invention, widely varying proportions of the organosilanes and borate esters may be used. More particularly, the base component may contain an organosilane and from 0 to 95% by weight of borate ester and preferably from 25 to by weight.
The amount of base component which is used in the hydraulic fluid of this invention can vary widely. Generally the base component will constitute at least about 20 percent by weight of the fluid and preferably at least about 40 percent by weight based on the total weight of the fluid composition.
Various diluents, inhibitors and other additives well known in the hydraulic fluid art may be added to the organosilane containing base component if desired. For example, the diluent portion may consist of one or more glycol monoethers or diethers of the formula:
wherein R is alkyl of 1 to 4 carbon atoms, R is alkylene of 2 to 4 carbon atoms, R is hydrogen or alkyl of from 1 to 4 carbon atoms and y is an integer of from 2 to 4. The R, R and R groups may be straight chained or branched and the alkylene oxide group (O-R,,) in the above formula may include mixtures of said alkylene oxides. Additionally, one or more glycols such as the alkylene glycols having for example, the following formula may be used:
HO (R 0) H wherein R is alkylene of from 2 to 3 carbon atoms and z is an integer of from 1 to 5.
Illustrative of the above-described diluents are the fol lowing: diethylene glycol monoethyl ether, diethylene glycol-monobutyl ether, triethylene glycol monomethyl ether, triethylene glycol monoethyl ether, tetraethylene glycol monomethyl ether, ethylene glycol, propylene glycol, diethylene glycol and tetraethylene glycol. Various other diluents and mixtures thereof, which are well known in the art may also be used with the organosilane containing base component of this invention. US. Pat. 3,377,288 and 5 applications 717,996 and 717,997, previously noted, disclose various diluents which may be utilized.
Generally the particular amount of diluents which is used is not critical and widely varying amounts may be used. More particularly, the diluent components may constitute from up to about 80 percent by weight of the fluid and preferably from about 20 to about 60 percent.
Various additives may be added to the hydraulic fluids of this invention containing the organosilane base component-to control or modify various chemical and physical properties. Among the various types of additives which can be added to the hydraulic fluids of this invention are included inhibitors for pH and corrosion control, antioxidants, rust inhibitors, viscosity index improvers, pour point depressants, lubricating additives, antifoamants, stabilizers, vapor phase corrosion inhibitors, rubber swelling adjusters, demulsifiers, dyes and odor suppressants. Generally, the total amount of additives which may be incorporated into the fluid composition will vary between about 0.01 to about 20 percent, preferably from about 0.1 to 8 percent and more preferably from about 0.2 to about percent by weight, based on the total weight of the hydraulic fluid composition.
For example, alkaline inhibitors for pH and corrosion control can be employed in an amount sufficient to maintain alkaline conditions in the fluid compositions, e.g. at a pH value of from about 7.0 to about 11.5 if desired. These inhibitors are generally added in an amount of from about 0.01 to about 8.0 percent by weight based on the total weight of fluid composition and preferably from about 0.5 to about 6.0 percent. Useful alkaline inhibitors include for example: alkali metal borates such as sodium borate and potassium tetraborate, alkali metal salts of higher fatty acids such as potassium oleate, the potassium soap of rosin or tall oil fatty acids, amines such as morpholine and ethanolamine and amine salts such as monoor dibutyl ammonium borates.
An antioxidant may be used, if desired. Typical antioxidants include, 2,2-di-(4-hydroxypheny1)propane, phenothiazine, amines such as phenyl-alpha-naphthylamine and hindered phenols such as dibutyl cresol. Generally, the amount of antioxidant used will vary from 0 to about 3 percent by weight and preferably from about 0.001 to about 2 percent by weight based on the total weight of the fluid composition.
Additionally, other additives if desired, may be incorporated into the fluid composition. For example, corrosion inhibitors such as butynediol and rubber swelling adjusters such as dodecyl benzene may be used.
The above-noted inhibitors and additives are merely exemplary and are not intended as an exclusive listing of the many well-known materials which can be added to fluid compositions to obtain various desired properties. Other illustrations of additives and diluents which may be used can be found in US. Pat. 3,377,288 and copending applications 717,996 and 717,997 previously noted and in Introduction to Hydraulic Fluids by Roger -E. Hatton, Reinhold Publishing Corp. (1962).
The following examples are further illustrative of this invention.
EXAMPLE I Percent by weight [CH3 (OCH2CH2)20] 2Si(CH )2 99.8 Tolutriazole 0.1 Bisphenol A 0.1
6 fluid (B.P. 550 F.) which showed a drop of about 270 F. to about 280 F.
Other properties of this fluid are as follows:
Kin. viscosity:
At 40 F. 43.5 cs. At 212 F. 1.14 cs. Pour point Below F. 'Flash point 320 F. Water Tolerance Test at -40 F.
and F. Passed.
All the above tests and all tests for the remaining examples were run in accordance with SAE specification J 1703a.
EXAMPLE 11 Percent by weight [CH (OCH CH O] Si(CH 99.8 Tolutriazole 0. 1 Bisphenol A 0.1
This composition was tested in the same manner as Example I and showed the following properties:
Reflux boiling point 625 F. Wet reflux boiling point (3.5% water added) 405 F. Kin. viscosity:
40 -F. 1800s. 212 F. 1.73 cs. Pour point Below 85 F. Flash point 385 F. Water Tolerance Test at -40 F.
and 140 F. Passed.
EXAMPLE III Percent by weight [CH (OCH CH 0] SiCH 99.8 Tolutriazole 0.1 Bisphenol A 0.1
The following properties obtained in accordance with SAE J 1703a were found:
Thefollowing properties obtained in accordance with SAE I 1703 were found:
Reflux boiling point, F. 552 Wet reflux boiling point (3.5% water added), F. 404 Kin. viscosity at 40 F., cs. 1270 Water tolerance Pass Chemical stability Pass Compatability Pass 7 EXAMPLE V Percent by weight 030] 3 10.0 [CH3 30'] 3B CH (OCH CH OH 9.0 C H (OCH CH OH 15.0 Monoethanolamine 1.0
The following properties obtained in accordance with The following properties obtained in accordance with SAE J 1703 were found:
Reflux boiling point, F. 545
Wet reflux boiling point (3.5 Water added), F. 384
Kin. viscosity at 40 F., cs. 1140 Water tolerance Pass Chemical stability =Pass Compatability Pass EXAMPLE VII Percent by weight [CH (OCH CH O] Si(CH 10.0
[(CH CH O) CH a 60.0
C H (OCH CH OH 5.0 Monoethanolamine 1.0 VPI 260 (dicyclohexylammonium nitrite) 0.1
The following properties obtained in accordance with SAE J 1703 were found:
Reflux boiling point, F. 524 Wet reflux boiling point (3.5% water added), F. 398 Kin. viscosity at 40 F., cs 3140 Water tolerance Pass Chemical stability 'Pass Compatability Pass EXAMPLE VIII Percent by weight [CH (OCH CH O] Si(CH 25.0 [CH (OCH CH O] B 56.3
C H (OCH CH OH 12.7 Diethanolamine 1.26 Sodium nitrite 0.02 Tolutriazole 0.07
The following properties obtained in accordance with SAE J 1703 were found:
Reflux boiling point, F. 554 Wet reflux boiling point (3.5% water added), F. 430 Viscosity at 40 F., cs. 800
What is claimed is: 1. A hydraulic fluid composition consisting essentially of:
(a) at least about 20 percent by weight, based on the total weight of the hydraulic fluid composition of a base component containing at least one organosilane of the formula:
(Rio-supp r.-.
wherein R is selected from the group consisting of alkyl of 1 to 10 carbon atoms and an aryl group of 6 to 10 carbon atoms, R is an alkyl group of 1 to 4 carbon atoms, R" is alkylene of from 2 to 4 carbon atoms, y is an integer of 1 to 5 and z is an integer of 1 to 3 (b) from 0 to about percent by weight, based on the total weight of the hydraulic fluid composition, of at least one diluent selected from the group consisting of:
(i) glycol ethers having the formula:
wherein R is alkyl of 1 to 4 carbon atoms, R is alkylene of 2 to 4 carbon atoms, R is selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms and y is an integer of 2 to 4, and
(ii) a glycol of the formula:
wherein R is alkylene of from 2 to 3 carbon atoms and z is an integer of from 1 to 5 and (c) from about 0.01 to about 20 percent by weight,
based on the total weight of the hydraulic fluid composition, of an additive which is an alkaline inhibitor for pH and corrosion control.
2. The composition of claim 1 which contains from about 0.01 to about 8.0 percent by weight of said alkaline inhibitor for pH and corrosion control.
3. The composition of claim 1 which contains at least about 40 percent by weight of said organosilane base component.
4. The composition of claim 3 which contains from about 20 to about 60 percent by weight of said diluent.
5. The composition of claim 1 wherein said additive is an antioxidant.
6. The composition of claim 1 wherein said additive is a rubber swelling adjuster.
7. The composition of claim 1 wherein said alkaline inhibitor is used in an amount of from about 0.5 to about 6.0% by weight, based on the total weight of the hydraulic fluid composition.
8. The composition of claim 5 wherein said antioxidant is used in an amount of from about 0.001 to about 2% by weight, based on the total weight of the hydraulic fluid composition.
9. The composition of claim 1 wherein said additive is a mixture of an alkaline inhibitor for pH and corrosion control and an antioxidant.
10. The composition of claim 9, wherein in said organosilane R is methyl and R methyl.
11. The composition of claim 10, wherein in said organosilane R" contains two carbon atoms, y is 2 and z is 2.
12. The composition of claim 10, wherein in said organosilane -R" contains two carbon atoms, y is 3 and z is 2.
13. The composition of claim 10, wherein in said organosilane R" contains two carbon atoms, y is 3 and z is 3.
14. The composition of claim 1 wherein the base component contains from about 0 to about percent by weight, based on the total Weight of base component, of at leagt one borate ester selected from the group consistmg 0 wherein R is an alkyl of from 1 to 4 carbon atoms, x is an integer of from 2 to 4 and y is an integer of from 2 to 4,
9 wherein R is alkyl of from 1 to 4 carbon atoms, R and R are independently selected from the group consisting of hydrogen and methyl, m and n are positive integers whose sum is from 2 to 20, and with the proviso that one of R and R is methyl and one of R and R is hydrogen wherein R is alkyl of from 1 to 4 carbon atoms, Rg is a heteric oxyalkylene chain of the formula:
[( cH2cH2), 2 3)SJ integers independently selected in each chain and whose sum in each chain is from 2 to 20, and with the proviso that in no more than two of the chains is the sum of n and m the same (e) R KOCHzCHR1)m(OCHgCHRl)nOk 11.1(0cH,cHR1)m(0CH,cHR1)n0 )0 (RICHCHIO) n-(R1CHCHz0)m]R; B
o mcnomo nnlcnommmlm wherein R and R are independently selected from the group consisting of hydrogen and methyl; R R R and R are each an independently selected alkyl group having from 1 to 4 carbon atoms and n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to and (1) R1[(() CHzCHROnr-(OCHzCHRa) 110k B-O-Ra where R and R are independently selected from the group consisting of hydrogen or methyl; R and R are each an independently selected alkyl group having from 1 to 4 carbon atoms; R is the organic residue exclusive of reactive hydroxyl groups of a polyol, p is an integer of from 2 to 6 inclusive and n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to 20.
15. The composition of claim 14 wherein said additive is an antioxidant.
16. The composition of claim 14 wherein said organosilane has the formula:
17. The composition of claim 14 wherein said organosilane has the formula:
[ 3 z z) s z 3 2 and said borate ester has the formula:
[CH OCHgCHg) O] B0(CH CH O B z 2 a al 2 18. In the operation of a fluid pressure operative device which uses hydraulic pressure transmission fluid, the improvement comprising using as said hydraulic pressure transmission fluid a composition including as the base component at least one organosilane of the formula:
wherein R is selected from the group consisting of alkyl of 1 to 10 carbon atoms and aryl of 6 to 10 carbon atoms, R is an alkyl group of 1 to 4 carbon atoms, R is alkylene of from 2 to 4 carbon atoms, y is an integer of 1 to 5 and z is an integer of 1 to 3.
19. The method of claim 18 wherein the base component contains from 0 to about percent by weight, based on the total weight of base component, of at least one borate ester selected from the group consisting of:
wherein R is an alkyl of from 1 to 4 carbon atoms, x is an integer of from 2 to 4 and y is an integer of from 2 to 4 wherein R is alkyl of from 1 to 4 carbon atoms, R and R are independently selected from the group consisting of hydrogen and methyl, m and n are positive integers whose sum is from 2 to 20, and with the proviso that one of R and R is methyl and one of R and \R is hydrogen wherein R is alkyl of from 1 to 4 carbon atoms, Rg is a heteric oxyalkylene chain of the formula:
wherein the sum of r and s is not more than 20 and wherein the weight percent of the oxyethylene units is not less than 20 based on the total weight of all the oxyalkylene units ((1) /O (RrOHCHzO)n(R5CHCHz0)mT1 B-O(RsCHCHgO)n(R CHCH2O)mTg wherein T T and T are each an independently selected alkyl group having from 1 to 4 carbon atoms; R R R R R and R are independently selected from the group consisting of hydrogen and methyl, n and m are positive integers independently selected in each chain an] whose sum in each chain is from 2 to 20, and with the proviso that in no more than two of the chains is the sum of n and m the same wherein R and R are independently selected from the group consisting of hydrogen and methyl; R R R and R are each an independently selected alkyl group having from 1 to 4 carbon atoms and n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to 20 and where R and R are independently selected from the group consisting of hydrogen or methyl; R and R are each an independently selected alkyl group having from 1 to 4 carbon atoms; R is the organic residue exclusive of reactive hydroxyl groups of a polyol, p is an integer of from 2 to 6 inclusive and n and m are positive integers independently selected in each chain and whose sum in each chain is from 2 to 20.
1 1 1 2 20. The method of claim 18 wherein said hydraulic 3,172,899 3/ 1965 'Bailey 252-78X pressure transmission fluid contains from about 0.01 to 3,308,149 3/ 1967 Schenck et a1. 260-4488 R about 20% by weight, based on the total weight of the hy- 3,316,287 4/ 1967 Nunn et a1. 260-462 draulic fluid composition, of an alkaline inhibitor for pH 3,625,899 12/ 1971 Sawyer et a1 252-78 X and corrosion control. 5 3,635,825 1/1972 Sawyer et a1 25278 X 21. The method of claim 18 wherein said hydraulic FOREIGN PATENTS pressure transmission fluid contains from about 0.01 to about 20% by weight, based on the total weight of the 960240 6/1964 England 2604483 hydraulic fluid compositions of an antioxidant. 10 LEON D. ROSDOL, Primary Examiner References Cited H. A. PITLICK, Assistant Examiner UNITED STATES PATENTS U'S. Cl. XR 3,080,412 3/1963 Young 260-462 3,133,111 5/1964 Wheeler 25249.6 X 15 R, 4 2 R mg UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,814,691. Dated June 4, 1974 Inventor(s) David A. Csejka and Henry F. Lederle It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
In column 9, linev70, '1EH (0cE cH ojB H ['0(cH cH o H 7 n D Signed and sealed this 17th day of September 1974.
(SEAL) Attest:
McCOY M. GIBSON JR. C. MARSI ILL DANN T- Attesting Officer Commissloner of Patents
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00259894A US3814691A (en) | 1970-09-25 | 1972-06-05 | Alkyl(polyalkoxy)silanes as components in hydraulic fluids |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US7571970A | 1970-09-25 | 1970-09-25 | |
US00259894A US3814691A (en) | 1970-09-25 | 1972-06-05 | Alkyl(polyalkoxy)silanes as components in hydraulic fluids |
Publications (1)
Publication Number | Publication Date |
---|---|
US3814691A true US3814691A (en) | 1974-06-04 |
Family
ID=26757205
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00259894A Expired - Lifetime US3814691A (en) | 1970-09-25 | 1972-06-05 | Alkyl(polyalkoxy)silanes as components in hydraulic fluids |
Country Status (1)
Country | Link |
---|---|
US (1) | US3814691A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3951832A (en) * | 1974-11-13 | 1976-04-20 | Texaco Inc. | Stabilized polysiloxane-polyglycol foam inhibitors for mineral oils |
US4016088A (en) * | 1973-09-25 | 1977-04-05 | Castrol Limited | Hydraulic fluids |
US4019997A (en) * | 1974-02-04 | 1977-04-26 | General Electric Company | Silicone fluid useful as a brae fluid |
DE2652719A1 (en) * | 1975-11-21 | 1977-05-26 | Castrol Ltd | SILANE DERIVATIVES AND HYDRAULIC FLUIDS CONTAINING THEM |
FR2395308A1 (en) * | 1977-06-24 | 1979-01-19 | Castrol Ltd | COMPOSITIONS OF FLUIDS CONTAINING IN PARTICULAR AN OXYSILANE |
US4141851A (en) * | 1975-11-21 | 1979-02-27 | Castrol Limited | Silane derivatives |
US4260505A (en) * | 1978-10-25 | 1981-04-07 | Olin Corporation | Tris-(polyalkoxyalkylated) isocyanurate compounds and their use as functional fluids |
US4332957A (en) * | 1980-12-22 | 1982-06-01 | National Distillers & Chemical Corp. | Phenoxyalkoxy silanes |
EP4227314A1 (en) | 2022-02-09 | 2023-08-16 | Basf Se | Method for the preparation of organic silicon compounds |
-
1972
- 1972-06-05 US US00259894A patent/US3814691A/en not_active Expired - Lifetime
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4016088A (en) * | 1973-09-25 | 1977-04-05 | Castrol Limited | Hydraulic fluids |
US4019997A (en) * | 1974-02-04 | 1977-04-26 | General Electric Company | Silicone fluid useful as a brae fluid |
US3951832A (en) * | 1974-11-13 | 1976-04-20 | Texaco Inc. | Stabilized polysiloxane-polyglycol foam inhibitors for mineral oils |
DE2652719A1 (en) * | 1975-11-21 | 1977-05-26 | Castrol Ltd | SILANE DERIVATIVES AND HYDRAULIC FLUIDS CONTAINING THEM |
US4141851A (en) * | 1975-11-21 | 1979-02-27 | Castrol Limited | Silane derivatives |
FR2395308A1 (en) * | 1977-06-24 | 1979-01-19 | Castrol Ltd | COMPOSITIONS OF FLUIDS CONTAINING IN PARTICULAR AN OXYSILANE |
US4260505A (en) * | 1978-10-25 | 1981-04-07 | Olin Corporation | Tris-(polyalkoxyalkylated) isocyanurate compounds and their use as functional fluids |
US4332957A (en) * | 1980-12-22 | 1982-06-01 | National Distillers & Chemical Corp. | Phenoxyalkoxy silanes |
FR2496667A1 (en) * | 1980-12-22 | 1982-06-25 | Nat Distillers Chem Corp | NOVEL PHENOXYALCOXYSILANES AND PROCESS FOR THEIR PREPARATION |
EP4227314A1 (en) | 2022-02-09 | 2023-08-16 | Basf Se | Method for the preparation of organic silicon compounds |
WO2023152001A1 (en) | 2022-02-09 | 2023-08-17 | Basf Se | Process for the preparation of organic silicon compounds |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4151099A (en) | Water-based hydraulic fluid and metalworking lubricant | |
US3711412A (en) | Low-water sensitive hydraulic fluids containing borate esters and formals | |
US4312768A (en) | Synergistic polyether thickeners for water-based hydraulic fluids | |
US3005776A (en) | Hydraulic fluid composition | |
US4287077A (en) | Glycol compositions containing an ether modified silicone to inhibit gelling | |
US3814691A (en) | Alkyl(polyalkoxy)silanes as components in hydraulic fluids | |
US4725405A (en) | Organosiloxane-silicate copolymer antifreeze composition with nitrate corrosion inhibitor | |
US4313836A (en) | Water-based hydraulic fluid and metalworking lubricant | |
US4702854A (en) | Water-based hydraulic fluids comprising poly-oxazines or poly-oxazolines | |
US4686058A (en) | Thickened-water based hydraulic fluids | |
JP5480285B2 (en) | Low viscosity functional fluid | |
US3798164A (en) | Polyoxyalkylene bis-thiourea extreme pressure agents and methods of use | |
EP0061823B1 (en) | Synergistically thickened water-based hydraulic or metal-working fluid | |
US3669884A (en) | Methyl alkyl silicone grease containing zinc naphthenate | |
US4552686A (en) | Corrosion inhibiting composition and method | |
US4048084A (en) | Functional fluid systems containing alkoxysilane cluster compounds | |
CA1084036A (en) | Hydraulic fluid compositions | |
US3592772A (en) | Functional fluids containing ammonia for preventing cavitation damage | |
EP0055488B1 (en) | Water-based energy transmitting fluid composition | |
US3098825A (en) | Non-corrosive hydraulic fluids | |
JP4812360B2 (en) | Hydrous hydraulic fluid composition and kinematic viscosity stabilizer used therefor | |
EP0273460B1 (en) | Energy transmitting fluid | |
US4048083A (en) | Functional fluid systems containing alkoxysilanol cluster compounds | |
US4664833A (en) | Organosiloxane-silicate copolymer antifreeze composition with nitrate corrosion inhibitor | |
CA1163041A (en) | Synergistically-thickened hydraulic fluid utilising alpha-olefin oxide modified polyethers |