US2189788A - Lubricant - Google Patents
Lubricant Download PDFInfo
- Publication number
- US2189788A US2189788A US708410A US70841034A US2189788A US 2189788 A US2189788 A US 2189788A US 708410 A US708410 A US 708410A US 70841034 A US70841034 A US 70841034A US 2189788 A US2189788 A US 2189788A
- Authority
- US
- United States
- Prior art keywords
- lubricant
- oil
- amine
- mixture
- base
- 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
- 239000000314 lubricant Substances 0.000 title description 72
- 239000002585 base Substances 0.000 description 32
- 239000003921 oil Substances 0.000 description 30
- 235000019198 oils Nutrition 0.000 description 30
- 239000000203 mixture Substances 0.000 description 24
- 150000001875 compounds Chemical class 0.000 description 21
- 239000000463 material Substances 0.000 description 21
- -1 aliphatic amino compound Chemical class 0.000 description 16
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000002184 metal Substances 0.000 description 14
- 230000007797 corrosion Effects 0.000 description 12
- 238000005260 corrosion Methods 0.000 description 12
- 235000014113 dietary fatty acids Nutrition 0.000 description 10
- 229930195729 fatty acid Natural products 0.000 description 10
- 239000000194 fatty acid Substances 0.000 description 10
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 9
- 239000010687 lubricating oil Substances 0.000 description 9
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- 238000009835 boiling Methods 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- 238000005461 lubrication Methods 0.000 description 7
- 230000002378 acidificating effect Effects 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 230000001050 lubricating effect Effects 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 229910002804 graphite Inorganic materials 0.000 description 5
- 239000010439 graphite Substances 0.000 description 5
- 235000013980 iron oxide Nutrition 0.000 description 5
- 230000003472 neutralizing effect Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000004519 grease Substances 0.000 description 4
- 150000002832 nitroso derivatives Chemical class 0.000 description 4
- 230000009972 noncorrosive effect Effects 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 239000000344 soap Substances 0.000 description 4
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- OOHAUGDGCWURIT-UHFFFAOYSA-N n,n-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 description 3
- 150000002828 nitro derivatives Chemical class 0.000 description 3
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- YXAOOTNFFAQIPZ-UHFFFAOYSA-N 1-nitrosonaphthalen-2-ol Chemical compound C1=CC=CC2=C(N=O)C(O)=CC=C21 YXAOOTNFFAQIPZ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 239000002199 base oil Substances 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 230000014509 gene expression Effects 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 238000005065 mining Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- 235000010288 sodium nitrite Nutrition 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- SYUYTOYKQOAVDW-UHFFFAOYSA-N 2-nitrosonaphthalen-1-ol Chemical compound C1=CC=C2C(O)=C(N=O)C=CC2=C1 SYUYTOYKQOAVDW-UHFFFAOYSA-N 0.000 description 1
- SEEZWGFVHCMHJF-UHFFFAOYSA-N 2-nitrosophenol Chemical class OC1=CC=CC=C1N=O SEEZWGFVHCMHJF-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000010727 cylinder oil Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 229940031098 ethanolamine Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000004807 localization Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- CLZGJKHEVKJLLS-UHFFFAOYSA-N n,n-diheptylheptan-1-amine Chemical compound CCCCCCCN(CCCCCCC)CCCCCCC CLZGJKHEVKJLLS-UHFFFAOYSA-N 0.000 description 1
- DIAIBWNEUYXDNL-UHFFFAOYSA-N n,n-dihexylhexan-1-amine Chemical compound CCCCCCN(CCCCCC)CCCCCC DIAIBWNEUYXDNL-UHFFFAOYSA-N 0.000 description 1
- LYPCJQNBARLNPU-UHFFFAOYSA-N n-aminooxy-n-phenylnitrous amide Chemical compound NON(N=O)C1=CC=CC=C1 LYPCJQNBARLNPU-UHFFFAOYSA-N 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 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
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- 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
- 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
- C10M2201/086—Chromium 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/18—Natural waxes, e.g. ceresin, ozocerite, bees wax, carnauba; Degras
-
- 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
- C10M2207/08—Aldehydes; Ketones
-
- 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
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
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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
- 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
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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
- 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
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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
- 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
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/20—Containing nitrogen-to-oxygen bonds
- C10M2215/202—Containing nitrogen-to-oxygen bonds containing nitro groups
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/20—Containing nitrogen-to-oxygen bonds
- C10M2215/204—Containing nitrogen-to-oxygen bonds containing nitroso groups
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/26—Amines
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Definitions
- the present invention relates to greatly improved lubricants for various uses and to the process of producing the same.
- the invention involves the addition of a compound or compounds to an I ordinary lubricant base.
- the lubricant thereby produced is far superior to the base lubricant treated by the addition of the compound or compounds in that it has a greater spreading power on metal surfaces, adheres more tenaciously to metal surfaces, thereby imparting greater lubrication under pressure, and materially reduces the problem of condensation and its efiEects.
- the improved lubricant is not affected by the normal temperature changes ordinarily g5 encountered in use to the same extent as the base lubricant and the improvement in this regard is substantial.
- a lubricant produced in accordance with my invention has effective protracted corrosion preventive properties, counteracts the effects of thin oxide films present prior to the application of the lubricant, has a low surface tension, and is free from graphite, heavy metals and their salts.
- the invention contemplates the use of or combination of aliphatic amino compounds and those cyclic amines exhibiting aliphatic amine properties, so that it will be understood the expression aliphatic amino compound includes those cyclic amines exhibiting such properties.
- aliphatic amino compound includes those cyclic amines exhibiting such properties.
- the aliphatic amine compound is added either alone or in combination with other ingredients, as will be set forth hereinafter, to an oil which will be referred to as the base lubricant.
- crank case or cylinder oil can be created by adding one or more aliphatic amines to an ordinary lubricating oil intended for this a purpose.
- a and in fact practically all kinds of lubricants can be made by incorporating aliphatic amino com- 10 pounds with present day lubricating mediums.
- aliphatic amines it has been found that a very satisfactory lubricant can be made by the addition of only the amine, while in other cases the amine can be treated with a w fatty acid and/or an alcohol, and/or ketones, and/or cyclic esters.
- the addition of nitro, nitro and nitroso reducing compounds may be used to advantage.
- the viscosity or S In addition to controlling the viscosity or S.
- the mode of combining the materials can be so handled to produce either a thicker or a thinner body lubricant from the same base as lubricant.
- Step (A) Heat about one mole weight of an aliphatic amine, for example about 149.15 lbs. of triethanol amine or approximately 61.06 lbs. of mono ethanol amine and the like about 0.77 mole weight of a fatty acid, for example approximately 5 225 lbs. of oleic acid, or 227 lbs. of stearic acid or the like; then heat this mixture at elevated temperatures within the practical range below the boiling point of the particular amine which is present. It is desirable to stir the mixture during 40 the reaction or 'the ingredients can be heated separately and then run through a colloidal mill.
- an aliphatic amine for example about 149.15 lbs. of triethanol amine or approximately 61.06 lbs. of mono ethanol amine and the like about 0.77 mole weight of a fatty acid, for example approximately 5 225 lbs. of oleic acid, or 227 lbs. of stearic acid or the like.
- Step (13) Mix approximately 0.87 mole weight of an inorganic nitrite, for example lbs. of sodium nitrite, which serves as a reducing agent, 5 and about 14 mole weight of hot, nearly boiling water.
- an orgaric nitro redu ing compound such as the nitruso naphthols, nitro phenols, amino-nitroso-phenyl-hydroxylamine, hydroxy nitro compounds, nitro phenols, and the like.
- a suitable solvent consists in dissolving about 2.8 lbs. of alpha-nitrosobeta-naphthol in about 63 lbs. of denatured al- '5 cohol or about 25 lbs. of an ester of phthalic acid such as dibutyl or diethyl phthalate.
- Th nitrocompound is more readily dissolved at slightly elevated temperatures, although excessively high temperatures should not be resorted
- Step (D) Combine the mixture formed by Step (B) with the mixture formed by Step (C), and then add this combination to the mixture formed by Step (A), mixing thoroughly.
- the base material which may, for the purposes of this application and for the sake of convenience, be referred to as the transmuting material.
- the resulting transmuting or base material' is then added to a suitable grade lubricating oil.
- the viscosity of the lubricant can be controlled in the manner of combining the base material and the oil so that either a high, medium, or low viscosity lubricant can be obtained. Very excellent results are obtained when about 65 parts of the transmuting or base material are added to about 400 parts of the lubricating oil, although obviously widely different proportions can be used.
- the oil is heated first and the base material then added.
- the base is heated first and the oil is added gradually during agitation, while to get a medium bodied lubricant the base is heated first and the oil is added a little faster than in the case when a thick lubricant is made.
- Practically the same method of control is employed when a colloidal mill is used instead of a mixer. With the use of the colloidal mill, the base and oil are heated separately to the desired temperatures. or may be premixed and heated depending upon the viscosity desired.
- Alcohol may be replaced by esters of phthalic acid, ketones, or other equivalent solvent materials.
- esters of phthalic acid ketones, or other equivalent solvent materials.
- lubricants contain either free fatty acids or other chemicals capable of reacting with some bearing materials forming either soaps or chemical compounds, thereby ruining the bearing; for example, in case of copper lead bearings when in contact with lubricating oils containing free oleic acid which forms a soap with the lead and causes material damage.
- My base material can be modified for this particular use by changing the amount of the fatty acid.
- a lubricant to be applied with a pressure gun for example, chassis lubrication
- a high viscosity lubricant so-called solid lubricant.
- Pressure gun lubricants, shipping compounds, and drawing compounds can all be made by proper control and/or by incorporating suitable soaps and the like.
- Example (1) To produce a crank case oil, an aliphatic amine or a mixture of aliphatic amines can be added to the base lubricant. Triamyl amine or trihexyl amine, or triheptyl amine are examples of the aliphatic amines that can be added to an ordinary oil such as a steam refined oil to give very satisfactory results for crank case or equivalent purposes.
- Example (2) To produce a spring lubricant where a lower surface tension is desired than in the case of the crank case oil and where greater adhesion to the metal serves to advantage to keep the springs well lubricated, a mixture of an aliphatic amine or mixture of aliphatic amines and a fatty acid can be added to the oil base.
- the oleic, acid is an example of a fatty acid which will work satisfactorily in this mixture.
- Example (3) To produce another mixture that is also useful as a crank case lubricant or as a differential and transmission lubricant, a mixture of Examples (1) and (2) plus an alcohol can be used. Butyl alcohol is mentioned as one form of alcohol that has given satisfactory results. This mixture, when added to the base oil, offers advantages in solving condensation problems and in decreasing surface tension. This mixture also lessens condensation troubles and the addition of the alcohol assists to reduce the solidification point. As a modification of this example, Example (2) plus alcohol results in an excellent rear end lubricant free from condensation troubles.
- Example (4) .-Contemp1ates the use of nitro, nitroso, hydroxy-nitro, and nitroso compounds.
- a nitro reducing compound such as nitroso naphthol added to Example (1) appears to act with the aliphatic amines as do the nitroso phenols.
- the use of butyl alcohol or dibutyl phthalate apparently serves to promote a reaction between the nitro compound and the aliphatic amino compound.
- This mixture can be used as a crank case oil, and it has been found that the nitroso compounds aid in reducing or removing iron oxide films from the metal to be lubricated.
- the addition of the nitronitroso compounds increases the life of the lubricant in crank case, difierenti al, and rear end uses.
- Example (4) possesses advantages. over Examples (1), (2), and (3) in that among other properties it not only neutralizes acids and other corrosive agents, but it removes oxide films that may be present on the metal, thus always insuring practically oxide free and well lubricated surfaces.
- Spring lubricants should contain a substance or substances capable of acting as a rust preventative which will act or be efiective over a considerable period of time.
- iron oxides are formed which tend to prevent further corrosion provided the film of iron oxide is not broken at any point, but should, as is usually the case, the film become broken, the result is that the underlying metal is exposed and consequently the rate of corrosion will be greatly increased due to localization of the action of absorbing acidic gases giving to the lubricant the property of protecting metal from the action of carbon dioxide and other acidic gases and also neutralizing any free acid that might possibly be present. It also has a property of acting on mild iron oxide.
- the alpha-nitroso-beta-naphthol mentioned as one example is capable of forming complex salts. This aids in maintaining the metal free from corrosion.
- the lubricant When the sodium nitrite is added in the manner suggested (potassium or other alkali and alkaline earth nitrites), the lubricant has the property of gradual absorption of active oxygen and therefore there is little, if any, opportunity for metal oxidation. Furthermore, the compounds activity in this regard is practically coexistent with the life of the lubricant itself. It is my opinion that the nitro (nitroso, etc.) compound, in addition to forming complex salts with the iron salts, has the property of improving the lubricating value of the base oil.
- the lubricant has the further advantage in that the possible chance for the formation of electrolytic couples is practically absent.
- the above lubricant not only functions as a lubricant, but also serves as a corrosive preventive in addition to being able to counteract the effect of thin oxide films which may be present on the parts to be lubricated before the application of the lubricating material. These properties are so pronounced that the material may even be used to coat battery ground cables, brake cables, and similar devices where the prevention of corrosion is of outstanding importance.
- organic materials included in my lubricant do not depend upon the formation of oxide films, and furthermore substances which are normally capable of causing corrosion are counteracted before the metal surface itself is reacted with those substances.
- a lubricant is formed which will give utmost of protection to metal surfaces and actual use has shown it to be very satisfactory as an engine lubricant such as in the crank case of the ordinary automobile as a spring lubricant, spring grease, spring cover grease, transmission and differential uses, cup grease, and general chassis lubrication of automobiles, as drawing and shipping compounds, and in fact in all cases where a good lubricant is desired.
- soap may be added to the mixture, while the drawing and/ or shipping compound can be produced by simply diluting the oil and transmuting material mixture with water. Over three hundred thousand pounds of my improved lubricant have been sold and used in different forms.
- the viscosity of the lubricant is controlled not only by the ingredients added, but also by the manner of mixing, depending upon the particular use to which the lubricant is to be put.
- a non-corrosive lubricant comprising a lubricating oil having incorporated therein a small amount of a free aliphatic amine base having a boiling point of not less than 45.3" i for coun teracting corrosion, absorbing acidic gases, and neutralizing acids, and a. small amount of an organic nitro reducing compound for maintaining the functioning of the amine.
- a non-corrosive lubricant comprising a lubricatlng oil having incorporated therein a small amount of a free aliphatic amine base having a boiling point or not less than 453 F. for counteracting corrosion, absorbing acidic gases, and neutralizing acids, and a small amount of a nitroso compound for maintaining the functioning of the amine.
- a non-corrosive lubricant comprising a lubricating oil having incorporated therein a small amount of a tree aliphatic amine base having a boiling point of not less than 45.3" F. for counteracting corrosion, absorbing acidic gases, and neutralizing acids, and a small amount of a nitroso compound and an inorganic nitrite for maintaining the functioning of the amine.
- a non-corrosive lubricant comprising a lubricating oil having incorporated therein a high molecular weight fatty acid and an aliphatic amine bash having a boiling point of not less than 45.3" F., the molecular proportion of said base being in substantial excess of the molecular proportion of the fatty acid whereby there is present a small amount of free aliphatic amine base for counteracting corrosion, absorbing acidic gases, and neutralizing acids, and a small amount of an organic nitro reducing compound for maintaining the functioning of the free amine.
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- Chemical & Material Sciences (AREA)
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- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Feb. 13, 1940 um'rso STATES PATENT orrics Serial 1937 4 Claims.
The present invention relates to greatly improved lubricants for various uses and to the process of producing the same.
One of the biggest problems faced in the op- 5 eration and maintenance of machinery or any device including parts movable in contact with one another is that of lubrication. It is generally understood that present day lubricating oils including refined petroleum hydrocarbons,
fish oils, and vegetable oils, do not satisfactorily meet all of the demands put upon them in automobile and other industrial uses.
Broadly speaking, the invention involves the addition of a compound or compounds to an I ordinary lubricant base. The lubricant thereby produced is far superior to the base lubricant treated by the addition of the compound or compounds in that it has a greater spreading power on metal surfaces, adheres more tenaciously to metal surfaces, thereby imparting greater lubrication under pressure, and materially reduces the problem of condensation and its efiEects. Furthermore, the improved lubricant is not affected by the normal temperature changes ordinarily g5 encountered in use to the same extent as the base lubricant and the improvement in this regard is substantial. Also, a lubricant produced in accordance with my invention has effective protracted corrosion preventive properties, counteracts the effects of thin oxide films present prior to the application of the lubricant, has a low surface tension, and is free from graphite, heavy metals and their salts.
Broadly speaking, the invention contemplates the use of or combination of aliphatic amino compounds and those cyclic amines exhibiting aliphatic amine properties, so that it will be understood the expression aliphatic amino compound includes those cyclic amines exhibiting such properties. Forexample, dimethyl amine, mono, di, triamyl amine, hydroxy aliphatic amines such as mono, di, tri, ethanol amine, amylolamine, aliphatic poly amines such as ethylene diamine. The aliphatic amine compound is added either alone or in combination with other ingredients, as will be set forth hereinafter, to an oil which will be referred to as the base lubricant. I have discovered and demonstrated that an ordinary oil can be greatly improved by the addition of one or more of the aliphatic amino compounds either alone or in combination with other ingredients, the ingredients added to the oil being dependent upon the particular use or uses to which the oil or other lubriga cant is to be put. Therefore, lubricants designed Renewed November 5,
for a wide range of uses can be produced in accordance with my discoveries. For example, a very excellent crank case or cylinder oil can be created by adding one or more aliphatic amines to an ordinary lubricating oil intended for this a purpose. Also, automobile spring lubricants, automobile differential and transmission lubricants, mining machinery and equipment, steam engines,
A and in fact practically all kinds of lubricants can be made by incorporating aliphatic amino com- 10 pounds with present day lubricating mediums. With some of the aliphatic amines, it has been found that a very satisfactory lubricant can be made by the addition of only the amine, while in other cases the amine can be treated with a w fatty acid and/or an alcohol, and/or ketones, and/or cyclic esters. In still other cases, the addition of nitro, nitro and nitroso reducing compounds may be used to advantage. In addition to controlling the viscosity or S. A. E. rating 20 of the lubricant produced in accordance with my invention by proper selection of the base lubricant used, the mode of combining the materials can be so handled to produce either a thicker or a thinner body lubricant from the same base as lubricant.
As an example of one particular lubricant that can be produced in accordance with my invention and that has been found to give extremely satisfactory results, the following is set forth. so
Step (A) .Heat about one mole weight of an aliphatic amine, for example about 149.15 lbs. of triethanol amine or approximately 61.06 lbs. of mono ethanol amine and the like about 0.77 mole weight of a fatty acid, for example approximately 5 225 lbs. of oleic acid, or 227 lbs. of stearic acid or the like; then heat this mixture at elevated temperatures within the practical range below the boiling point of the particular amine which is present. It is desirable to stir the mixture during 40 the reaction or 'the ingredients can be heated separately and then run through a colloidal mill.
Step (13) .Mix approximately 0.87 mole weight of an inorganic nitrite, for example lbs. of sodium nitrite, which serves as a reducing agent, 5 and about 14 mole weight of hot, nearly boiling water.
Step (CL-Mix approximately 0.017 mole weight of an orgaric nitro redu ing compound such as the nitruso naphthols, nitro phenols, amino-nitroso-phenyl-hydroxylamine, hydroxy nitro compounds, nitro phenols, and the like, in a suitable solvent. One specific example consists in dissolving about 2.8 lbs. of alpha-nitrosobeta-naphthol in about 63 lbs. of denatured al- '5 cohol or about 25 lbs. of an ester of phthalic acid such as dibutyl or diethyl phthalate. Th nitrocompound is more readily dissolved at slightly elevated temperatures, although excessively high temperatures should not be resorted to as this promotes decomposition of the nitro compounds.
Step (D) .Combine the mixture formed by Step (B) with the mixture formed by Step (C), and then add this combination to the mixture formed by Step (A), mixing thoroughly. This then gives what I term the base material which may, for the purposes of this application and for the sake of convenience, be referred to as the transmuting material. The resulting transmuting or base material'is then added to a suitable grade lubricating oil.
In the production of a spring lubricant, excellent results can and have been obtained by adding the base material to a steam refined, Bright stock, or other suitable grade of oil, although obviously the invention is not in any way limited to the addition of the base material to any particular oil. However, it may be mentioned that the base material above described has been added to about 40,000 gallons of a steam refined sulphur free oil having a viscosity at 100 of 3390 and at 210 of 200-205, and extraordinarily satisfactory commercial results have been obtained. Large manufacturers of automobiles have purchased and are using substantial quantities of this particular mixture for spring lubricating purposes.
As stated above, the viscosity of the lubricant can be controlled in the manner of combining the base material and the oil so that either a high, medium, or low viscosity lubricant can be obtained. Very excellent results are obtained when about 65 parts of the transmuting or base material are added to about 400 parts of the lubricating oil, although obviously widely different proportions can be used.
Specimens covered with the above oil and base material mixture were exposed on the roof of one of the largest automobile manufacturer's research laboratories for about five months and'at the end of this time there was absolutely no evidenceof corrosion. Other tests showed that the oil and base material mixture maintained its lubricating qualities approximately ten times as long as the oil not including my transmuting material. Many other severe tests were made and in all cases the oil and base material mixture gave results far superior to the oil proper without the base material.
To produce a thinner lubricant, the oil is heated first and the base material then added. On the other hand,if a thicker lubricant is preferred, the base is heated first and the oil is added gradually during agitation, while to get a medium bodied lubricant the base is heated first and the oil is added a little faster than in the case when a thick lubricant is made. Practically the same method of control is employed when a colloidal mill is used instead of a mixer. With the use of the colloidal mill, the base and oil are heated separately to the desired temperatures. or may be premixed and heated depending upon the viscosity desired.
Since lubrication problems vary greatly, it is necessary for best results to produce different types of lubricants; that is, lubricants having somewhat different characteristics to meet diiferent problems. Where the need for a particular property or properties is pronounced, I have found that my improved lubricant can be modified to emphasize the desired property, so that by proper control of ingredients any specific lubricating problem can be coped with. In all cases, however, the use of an aliphatic amino compound is resorted to and the method of processing and specific materials added are controlled for the purposes Just stated.
In the case of producing a lubricant for automobile springs, in addition to the properties already mentioned, more friction is desirable, and this can be obtained by increasing the relative amount of water and amino fatty acid compound and/or by adding suitable resins and/or gums. On the other hand, where it is necessary or desirable to impregnate porous metal with a lubricant at elevated temperatures, glycerin or some high boiling point solvent, such as ethylene glycol, may be utilized in lieu of the water. Where dry lubrication, so to speak, is desired, waxes and gums can be incorporated with the base material instead of oil by selecting the proper solvent and amino fatty acid with which it may be peptized, although some gums and waxes are soluble in amino compounds themselves. Alcohol may be replaced by esters of phthalic acid, ketones, or other equivalent solvent materials. In those cases where it is necessary to avoid emulsification with water such as in steam motors, mining machinery, and the like, I have found it advisable to use some solvents other than water, glycerin, or alcohol, and an amino fatty acid compound capable of emulsifying the solvent with the oil and which will not emulsiiy water, for example, triamyl amine, oleate, or stearate.
Many present day lubricants contain either free fatty acids or other chemicals capable of reacting with some bearing materials forming either soaps or chemical compounds, thereby ruining the bearing; for example, in case of copper lead bearings when in contact with lubricating oils containing free oleic acid which forms a soap with the lead and causes material damage. My base material can be modified for this particular use by changing the amount of the fatty acid.
In the production of a lubricant to be applied with a pressure gun, for example, chassis lubrication, it is of course necessary to have a high viscosity lubricant, so-called solid lubricant. Pressure gun lubricants, shipping compounds, and drawing compounds, can all be made by proper control and/or by incorporating suitable soaps and the like.
As specific examples of some of the different types of lubricants and the manner of producing the same in accordance with my invention, the following outline is given:
Example (1).-To produce a crank case oil, an aliphatic amine or a mixture of aliphatic amines can be added to the base lubricant. Triamyl amine or trihexyl amine, or triheptyl amine are examples of the aliphatic amines that can be added to an ordinary oil such as a steam refined oil to give very satisfactory results for crank case or equivalent purposes.
Example (2).To produce a spring lubricant where a lower surface tension is desired than in the case of the crank case oil and where greater adhesion to the metal serves to advantage to keep the springs well lubricated, a mixture of an aliphatic amine or mixture of aliphatic amines and a fatty acid can be added to the oil base. The oleic, acid is an example of a fatty acid which will work satisfactorily in this mixture.
Example (3).-To produce another mixture that is also useful as a crank case lubricant or as a differential and transmission lubricant, a mixture of Examples (1) and (2) plus an alcohol can be used. Butyl alcohol is mentioned as one form of alcohol that has given satisfactory results. This mixture, when added to the base oil, offers advantages in solving condensation problems and in decreasing surface tension. This mixture also lessens condensation troubles and the addition of the alcohol assists to reduce the solidification point. As a modification of this example, Example (2) plus alcohol results in an excellent rear end lubricant free from condensation troubles.
Example (4) .-Contemp1ates the use of nitro, nitroso, hydroxy-nitro, and nitroso compounds. A nitro reducing compound such as nitroso naphthol added to Example (1) appears to act with the aliphatic amines as do the nitroso phenols. The use of butyl alcohol or dibutyl phthalate apparently serves to promote a reaction between the nitro compound and the aliphatic amino compound. This mixture can be used as a crank case oil, and it has been found that the nitroso compounds aid in reducing or removing iron oxide films from the metal to be lubricated. Experiments indicate that the addition of the nitronitroso compounds increases the life of the lubricant in crank case, difierenti al, and rear end uses.
Broadly speaking, the mixture of Example (4) possesses advantages. over Examples (1), (2), and (3) in that among other properties it not only neutralizes acids and other corrosive agents, but it removes oxide films that may be present on the metal, thus always insuring practically oxide free and well lubricated surfaces.
To illustrate the number of considerations that must be borne in mind in the production of a truly satisfactory lubricant, I will discuss a lubricant designed particularly for spring lubrication purposes, although of course it is to be clearly understood that my invention is in no way limited to any one type of lubricant or lubricants for any one particular field of use.
Spring lubricants should contain a substance or substances capable of acting as a rust preventative which will act or be efiective over a considerable period of time. Some attempts have been made to incorporate inorganic inhibiting compounds in oils but, so far as I have been able to ascertain, the use of inorganic inhibitors in lubricating oils has not proven satisfactory. Oxidizing agents, such as potassium dichromate, have been added to oils as inorganic inhibiting compounds. However, when applied to metal, iron oxides are formed which tend to prevent further corrosion provided the film of iron oxide is not broken at any point, but should, as is usually the case, the film become broken, the result is that the underlying metal is exposed and consequently the rate of corrosion will be greatly increased due to localization of the action of absorbing acidic gases giving to the lubricant the property of protecting metal from the action of carbon dioxide and other acidic gases and also neutralizing any free acid that might possibly be present. It also has a property of acting on mild iron oxide. The alpha-nitroso-beta-naphthol mentioned as one example is capable of forming complex salts. This aids in maintaining the metal free from corrosion.
When the sodium nitrite is added in the manner suggested (potassium or other alkali and alkaline earth nitrites), the lubricant has the property of gradual absorption of active oxygen and therefore there is little, if any, opportunity for metal oxidation. Furthermore, the compounds activity in this regard is practically coexistent with the life of the lubricant itself. It is my opinion that the nitro (nitroso, etc.) compound, in addition to forming complex salts with the iron salts, has the property of improving the lubricating value of the base oil. It will of course be appreciated that there may be some reactions that take place when all of the ingredients are mixed togther that we are not entirely familiar with or do not thoroughly understand, although the above expressions have been made to give my opinion as to what takes place based on the practical results which have been obtained. It may also be added that the lubricant has the further advantage in that the possible chance for the formation of electrolytic couples is practically absent. The above lubricant not only functions as a lubricant, but also serves as a corrosive preventive in addition to being able to counteract the effect of thin oxide films which may be present on the parts to be lubricated before the application of the lubricating material. These properties are so pronounced that the material may even be used to coat battery ground cables, brake cables, and similar devices where the prevention of corrosion is of outstanding importance.
,In my opinion, a desirable lubricant must be free from graphite, and it will be noted that no graphite is included in my improved lubricant consisting of the base lubricant and transmuting or base material. When a graphite lubricant is applied to spring leaves, for example, the lubricent is squeezed out under the pressure applied to the spring leaves and the residual graphite is forced into the minute pores of the metal, with the result that an electrolytic couple is then es-' tablished. This results in the liberation of hydrogen which partially escapes, and no doubt part of it becomes deposited in the pores of the spring leaves. The pressure normally present accelerates the well known effect of embrittling of the iron and, in addition, the iron is corroded and pitted by the electrolytic action just mentioned.
It is clear that in those cases where inorganic inhibitors are added to lubricants, the formation of protective films of iron oxides is depended upon which are readily broken thus permitting excessive and accelerated corrosion of the exposed areas.
organic materials included in my lubricant do not depend upon the formation of oxide films, and furthermore substances which are normally capable of causing corrosion are counteracted before the metal surface itself is reacted with those substances.
In view of the ability to compound my oil mixture to readily emulsify water, if so desired, the
In contradistinction to the em-] ployment of inorganic inhibiting. agents, the
acid compounds in the manner above suggested,
a lubricant is formed which will give utmost of protection to metal surfaces and actual use has shown it to be very satisfactory as an engine lubricant such as in the crank case of the ordinary automobile as a spring lubricant, spring grease, spring cover grease, transmission and differential uses, cup grease, and general chassis lubrication of automobiles, as drawing and shipping compounds, and in fact in all cases where a good lubricant is desired. In making the cup grease or a lubricant of similar characteristics, soap may be added to the mixture, while the drawing and/ or shipping compound can be produced by simply diluting the oil and transmuting material mixture with water. Over three hundred thousand pounds of my improved lubricant have been sold and used in different forms.
It will of course be understood that the viscosity of the lubricant is controlled not only by the ingredients added, but also by the manner of mixing, depending upon the particular use to which the lubricant is to be put.
I claim:
1. A non-corrosive lubricant comprising a lubricating oil having incorporated therein a small amount of a free aliphatic amine base having a boiling point of not less than 45.3" i for coun teracting corrosion, absorbing acidic gases, and neutralizing acids, and a. small amount of an organic nitro reducing compound for maintaining the functioning of the amine.
2. A non-corrosive lubricant comprising a lubricatlng oil having incorporated therein a small amount of a free aliphatic amine base having a boiling point or not less than 453 F. for counteracting corrosion, absorbing acidic gases, and neutralizing acids, and a small amount of a nitroso compound for maintaining the functioning of the amine.
3. A non-corrosive lubricant comprising a lubricating oil having incorporated therein a small amount of a tree aliphatic amine base having a boiling point of not less than 45.3" F. for counteracting corrosion, absorbing acidic gases, and neutralizing acids, and a small amount of a nitroso compound and an inorganic nitrite for maintaining the functioning of the amine.
4. A non-corrosive lubricant comprising a lubricating oil having incorporated therein a high molecular weight fatty acid and an aliphatic amine bash having a boiling point of not less than 45.3" F., the molecular proportion of said base being in substantial excess of the molecular proportion of the fatty acid whereby there is present a small amount of free aliphatic amine base for counteracting corrosion, absorbing acidic gases, and neutralizing acids, and a small amount of an organic nitro reducing compound for maintaining the functioning of the free amine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US708410A US2189788A (en) | 1934-01-26 | 1934-01-26 | Lubricant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US708410A US2189788A (en) | 1934-01-26 | 1934-01-26 | Lubricant |
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Publication Number | Publication Date |
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US2189788A true US2189788A (en) | 1940-02-13 |
Family
ID=24845692
Family Applications (1)
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US708410A Expired - Lifetime US2189788A (en) | 1934-01-26 | 1934-01-26 | Lubricant |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2445064A (en) * | 1939-10-30 | 1948-07-13 | Tootal Broadhurst Lee Co Ltd | Alkali metal hydroxide liquid reagent |
US2514017A (en) * | 1948-08-31 | 1950-07-04 | Shell Dev | Lubricant |
US3017362A (en) * | 1958-06-12 | 1962-01-16 | Universal Oil Prod Co | Hydrocarbon oil composition |
US3380918A (en) * | 1966-03-25 | 1968-04-30 | Chevron Res | Aryl nitroso compounds as lubricant additives |
US4125668A (en) * | 1976-09-10 | 1978-11-14 | Ball Brothers Research Corporation | Lubricants comprising dialkanolamine derivatives |
US4587026A (en) * | 1984-06-21 | 1986-05-06 | Mobil Oil Corporation | Multifunctional lubricant additives |
US20050082139A1 (en) * | 2003-08-22 | 2005-04-21 | Nissan Motor Co., Ltd. | Low-friction sliding member in transmission, and transmission oil therefor |
US20050100701A1 (en) * | 2003-08-08 | 2005-05-12 | Nissan Motor Co., Ltd. | Sliding member and production process thereof |
-
1934
- 1934-01-26 US US708410A patent/US2189788A/en not_active Expired - Lifetime
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2445064A (en) * | 1939-10-30 | 1948-07-13 | Tootal Broadhurst Lee Co Ltd | Alkali metal hydroxide liquid reagent |
US2514017A (en) * | 1948-08-31 | 1950-07-04 | Shell Dev | Lubricant |
US3017362A (en) * | 1958-06-12 | 1962-01-16 | Universal Oil Prod Co | Hydrocarbon oil composition |
US3380918A (en) * | 1966-03-25 | 1968-04-30 | Chevron Res | Aryl nitroso compounds as lubricant additives |
US4125668A (en) * | 1976-09-10 | 1978-11-14 | Ball Brothers Research Corporation | Lubricants comprising dialkanolamine derivatives |
US4587026A (en) * | 1984-06-21 | 1986-05-06 | Mobil Oil Corporation | Multifunctional lubricant additives |
US20090054277A1 (en) * | 2003-08-08 | 2009-02-26 | Nissan Motor Co., Ltd. | Sliding member and production process thereof |
US20050100701A1 (en) * | 2003-08-08 | 2005-05-12 | Nissan Motor Co., Ltd. | Sliding member and production process thereof |
US8575076B2 (en) | 2003-08-08 | 2013-11-05 | Nissan Motor Co., Ltd. | Sliding member and production process thereof |
US20050082139A1 (en) * | 2003-08-22 | 2005-04-21 | Nissan Motor Co., Ltd. | Low-friction sliding member in transmission, and transmission oil therefor |
US20080236984A1 (en) * | 2003-08-22 | 2008-10-02 | Nissan Motor Co., Ltd. | Low-friction sliding member in transmission, and transmission oil therefor |
US7650976B2 (en) | 2003-08-22 | 2010-01-26 | Nissan Motor Co., Ltd. | Low-friction sliding member in transmission, and transmission oil therefor |
US7318514B2 (en) * | 2003-08-22 | 2008-01-15 | Nissan Motor Co., Ltd. | Low-friction sliding member in transmission, and transmission oil therefor |
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