US2910437A - Stabilization of lubricants - Google Patents
Stabilization of lubricants Download PDFInfo
- Publication number
- US2910437A US2910437A US570420A US57042056A US2910437A US 2910437 A US2910437 A US 2910437A US 570420 A US570420 A US 570420A US 57042056 A US57042056 A US 57042056A US 2910437 A US2910437 A US 2910437A
- Authority
- US
- United States
- Prior art keywords
- grease
- inhibitor
- stabilization
- lubricants
- diaminodiphenyl ether
- 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 claims description 5
- 230000006641 stabilisation Effects 0.000 title description 3
- 238000011105 stabilization Methods 0.000 title description 3
- 239000003112 inhibitor Substances 0.000 claims description 14
- 230000000087 stabilizing effect Effects 0.000 claims description 6
- 230000006866 deterioration Effects 0.000 claims description 4
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 239000004519 grease Substances 0.000 description 32
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- 239000000654 additive Substances 0.000 description 6
- 230000006698 induction Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000523 sample Substances 0.000 description 4
- RDMFEHLCCOQUMH-UHFFFAOYSA-N 2,4'-Diphenyldiamine Chemical group C1=CC(N)=CC=C1C1=CC=CC=C1N RDMFEHLCCOQUMH-UHFFFAOYSA-N 0.000 description 3
- ABQAWYPFZVJRGM-UHFFFAOYSA-N 4-phenoxybenzene-1,3-diamine Chemical group NC1=CC(N)=CC=C1OC1=CC=CC=C1 ABQAWYPFZVJRGM-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- HGPXWXLYXNVULB-UHFFFAOYSA-M lithium stearate Chemical compound [Li+].CCCCCCCCCCCCCCCCCC([O-])=O HGPXWXLYXNVULB-UHFFFAOYSA-M 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- -1 alkylated diphenyl amines Chemical class 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000013068 control sample Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000007787 solid Substances 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
- 229910001369 Brass Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000283153 Cetacea Species 0.000 description 1
- 244000187656 Eucalyptus cornuta Species 0.000 description 1
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- HYJODZUSLXOFNC-UHFFFAOYSA-N [S].[Cl] Chemical class [S].[Cl] HYJODZUSLXOFNC-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- ZNZJJSYHZBXQSM-UHFFFAOYSA-N propane-2,2-diamine Chemical compound CC(C)(N)N ZNZJJSYHZBXQSM-UHFFFAOYSA-N 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 229940065287 selenium compound Drugs 0.000 description 1
- 150000003343 selenium compounds Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical class OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
- G01R17/00—Measuring arrangements involving comparison with a reference value, e.g. bridge
- G01R17/10—AC or DC measuring bridges
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
- C07C67/62—Use of additives, e.g. for stabilisation
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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
- C10M5/00—Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B5/00—Preserving by using additives, e.g. anti-oxidants
- C11B5/0042—Preserving by using additives, e.g. anti-oxidants containing nitrogen
- C11B5/005—Amines or imines
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
- G01R17/00—Measuring arrangements involving comparison with a reference value, e.g. bridge
-
- 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
- C10M2201/04—Elements
- C10M2201/041—Carbon; Graphite; Carbon black
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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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/10—Compounds containing silicon
- C10M2201/102—Silicates
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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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/10—Compounds containing silicon
- C10M2201/105—Silica
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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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
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- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
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- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/108—Residual fractions, e.g. bright stocks
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
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- C—CHEMISTRY; METALLURGY
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- C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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- C—CHEMISTRY; METALLURGY
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- 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
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- C—CHEMISTRY; METALLURGY
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- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
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- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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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
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- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/16—Naphthenic acids
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- 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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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
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- C10M2219/108—Phenothiazine
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Definitions
- the synthetic greases generally'are referred to as lithium base grease, sodium base-grease, calcium base grease, barium base-grease, strontium base 'grease, aluminum base grease, etc.
- These greases are solid or semi-solid gels and, in generaL-are prepared by the addition to mineral or synthetic oils of hydrocarbon-soluble metal soaps or salts of higher fatty acids as, for example, lithium stearate, calcium stearate, aluminum naphthenate, etc.
- the grease may contain thickening agents such as silica, carbon black, polyacrylatesftalc, etc.
- Another type of grease is prepared from oxidized petroleum wax, to which the saponifiable base is combined with the proper amount of the desired sapom'fying agent, and the resultant mixture processed to produce a grease.
- Other types of greases in which the features of the present invention are usable include petroleum grease, whale grease, wool grease, etc., and those made from inedible fats, tallow, butchers waste, etc.
- the present invention also is particularly applicable to the stabilization of lubricating oils, including those of petroleum or synthetic origin.
- the synthetic lubricants are of varied types including aliphatic esters, polyalkylene oxides, silicones, esters of phosphoric and silicic acids,
- aliphatic esters di-(Z-ethylhexyl) sebacate is being used on a comparatively large commercial scale.
- Other aliphatic esters include dialkyl azelates, dialkyl suberates,
- the inhibitor may be used along with other additives incorporated in the organic substance.
- the inhibitor may be used along with higher alcohols, esters, organic amines, poly butene, suI-furized fatty materials, sulfur chlorine compounds, 'dyes, perfumed materials, fillers, etc.
- a metal include methyl silicone, methylphenyl silicone, etc.
- the silicates include, for example, tetraisooctyl silicate, etc.
- the highly fiuorinated hydrocarbons include fluo rinated oil, perfiuorohydrocarbons, etc.
- the present invention relates to a method of stabilizing synthetic grease which comprises incorporating therein from about 0.1 to about 5% by weight of 2,4'-,diaminod.iphenyl ether.
- the present invention relates to a method of stabilizing lubricating oil against oxida tive deterioration which comprises incorporating therein a stabilizing concentration of a 2,4'-diaminodiphenyl ether.
- the present invention comprises a 2,4-diaminodipheny l ether.
- a preferred inhibitor is 2,4-diaminodiphenyl ether. 7
- the inhibitor will be utilized in a concentration of from about 0.0001% to about 5% by weight of the organic substance, although in some cases higher trial-kyl deactivator as, for example, disalicylal diamino propane, ethylene diamine tetra-acetic acid tetrasodium salt, etc., or to include other additives such as tricresyl phosphate,
- the inhibitor of the present invention may be prepared as amixture with one or more of these other additives and incorporated in this manner in the organic substance or components thereof.
- the inhibitor of the present invention may be incorporatedin the organic substance in any suitable manner and at any suitable stage of preparation.
- the inhibitor in an organic substance which comprises a mixture of several components, as for example, grease, the inhibitor may be added to one or more of the components of the grease prior to compositing and processing thereof or it may be added to the mix at any time, preferably before final processing in order to obtain intimate mixing and dissolving of the inhibitor in the grease.
- Example I 2,4'-diaminodiphenyl ether was utilized as an inhibitor in a lithium grease.
- the grease was prepared by mixing 91% of a Pennsylvania bright stock with 8% of lithium stearate. The mixture was heated at about 450 F. while agitating the same. Subsequently, the grease was cooled while agitating to 320 F. and, at this'temperature, 1% of 2,4'-diaminodiphenyl ether was added. Agitationwas continued and the mixture was allowed to cool to about 250 F. and the grease then further cooled slowly to room temperature.
- the stability of the grease was tested according to a modified Norma Hoffman method, 'in which a sample of I the grease is placed in a bomb in the presence of brass discs acting as an oxidation catalyst and oxygen is charged thereto. The bomb then is heated to 212 F., and the time required for a drop of 5 pounds pressure is taken as the induction period. In this run, a control sample of the grease (not containing this additive) had an induction period of 10.5 hours. On the other hand, a sample of the grease containing 1% by weight of 2,4- diaminodiphenyl ether had an induction period of 260 hours.
- the inhibitor of the present invention was exceptionally eliective in improving the stability of the grease.
- Example 11 This grease had a control (not containing this additive).
- Example Ill The grease used in this example was a syntheticgrease prepared in substantially the same manner described in Example I, except that 87% of di-Z-ethylhexyl sebacate was mixed with 12% lithium stearate. 1% by weight of 2,4- diaminodiphenyl ether was incorporated in the syn thetic grease. A control sample of the grease (not containing this additive) had an induction period of 17 hours. On the other hand, a sample of the grease containing 1% by weight of 2,4-diamino-dipheny1 ether did not undergo a pressure drop of one pound per square inch until after 318 hours exposure.
- a method of stabilizing a lubricant normally subject to oxidative deterioration which comprises incorporating 25 therein a stabilizing concentration otza' diniiaadiphen r ether.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Lubricants (AREA)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL102710D NL102710C (enrdf_load_stackoverflow) | 1956-03-09 | ||
| US570420A US2910437A (en) | 1956-03-09 | 1956-03-09 | Stabilization of lubricants |
| GB7219/57A GB819024A (en) | 1956-03-09 | 1957-03-05 | Improvements in or relating to the stabilizing of lubricating greases |
| DEU4409A DE1113785B (de) | 1956-03-09 | 1957-03-07 | Schmierfett auf der Basis von mineralischen, tierischen oder synthetischen OElen |
| ES0234133A ES234133A1 (es) | 1956-03-09 | 1957-03-08 | UN PROCEDIMIENTO PARA ESTABILIZAR UNA SUSTANCIA ORGáNICA CONTRA LA DETERIORIZACIoN OXIDATIVA |
| FR1172914D FR1172914A (fr) | 1956-03-09 | 1957-03-09 | Procédé pour la stabilisation de substances organiques |
| GB43340/60A GB899024A (en) | 1956-03-09 | 1960-12-16 | Alternating current bridge |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US570420A US2910437A (en) | 1956-03-09 | 1956-03-09 | Stabilization of lubricants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2910437A true US2910437A (en) | 1959-10-27 |
Family
ID=24279577
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US570420A Expired - Lifetime US2910437A (en) | 1956-03-09 | 1956-03-09 | Stabilization of lubricants |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US2910437A (enrdf_load_stackoverflow) |
| DE (1) | DE1113785B (enrdf_load_stackoverflow) |
| ES (1) | ES234133A1 (enrdf_load_stackoverflow) |
| FR (1) | FR1172914A (enrdf_load_stackoverflow) |
| GB (1) | GB819024A (enrdf_load_stackoverflow) |
| NL (1) | NL102710C (enrdf_load_stackoverflow) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2982729A (en) * | 1958-04-02 | 1961-05-02 | Universal Oil Prod Co | High temperature lubricating grease containing a p, p'-diaminodiphenylether |
| US3169926A (en) * | 1961-11-29 | 1965-02-16 | Universal Oil Prod Co | Stabilization of organic substances |
| US3208944A (en) * | 1962-11-19 | 1965-09-28 | Universal Oil Prod Co | Stabilization of lubricants |
| US3240706A (en) * | 1963-01-24 | 1966-03-15 | Universal Oil Prod Co | Stabilization of organic substances |
| US3330777A (en) * | 1966-03-16 | 1967-07-11 | Universal Oil Prod Co | Stabilization of organic substances |
| US4378298A (en) * | 1981-05-12 | 1983-03-29 | Uop Inc. | Imines of 2,4-diaminodiphenyl ethers as antioxidants for lubricating oils and greases |
| US4380497A (en) * | 1981-05-12 | 1983-04-19 | Uop Inc. | Amines of alkoxydiphenyl esthers as antioxidants and lubricating oils and greases containing same |
| US4386002A (en) * | 1981-05-12 | 1983-05-31 | Uop Inc. | Imines of aminodiphenyl esthers as antioxidants and lubricating oils and greases containing same |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114892176B (zh) * | 2022-05-12 | 2024-03-26 | 中山大学 | 有机硒在抑制碳钢在酸性溶液中腐蚀的应用和碳钢缓蚀剂 |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2048362A (en) * | 1934-05-04 | 1936-07-21 | Dow Chemical Co | Acid composition for treatment of deep wells |
| US2269265A (en) * | 1939-12-14 | 1942-01-06 | Socony Vacuum Oil Co Inc | Stabilized refined petroleum product |
| US2290860A (en) * | 1940-04-26 | 1942-07-28 | Standard Oil Co | Beneficiation of lubricating oils |
| US2350746A (en) * | 1941-11-26 | 1944-06-06 | Socony Vacuum Oil Co Inc | Mineral oil composition |
| US2367264A (en) * | 1940-09-30 | 1945-01-16 | Standard Oil Co | Beneficiating lubricants, etc. |
| US2440530A (en) * | 1944-11-04 | 1948-04-27 | Shell Dev | Stabilized organic compositions |
| US2523100A (en) * | 1947-05-17 | 1950-09-19 | Standard Oil Dev Co | Mineral oil composition and additive therefor |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2692288A (en) * | 1951-03-29 | 1954-10-19 | Eastman Kodak Co | Production of n-tertiary alkylated aromatic secondary diamines |
| DE929385C (de) * | 1952-04-23 | 1955-06-27 | Bayer Ag | Zusaetze fuer Schmiermittel |
-
0
- NL NL102710D patent/NL102710C/xx active
-
1956
- 1956-03-09 US US570420A patent/US2910437A/en not_active Expired - Lifetime
-
1957
- 1957-03-05 GB GB7219/57A patent/GB819024A/en not_active Expired
- 1957-03-07 DE DEU4409A patent/DE1113785B/de active Pending
- 1957-03-08 ES ES0234133A patent/ES234133A1/es not_active Expired
- 1957-03-09 FR FR1172914D patent/FR1172914A/fr not_active Expired
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2048362A (en) * | 1934-05-04 | 1936-07-21 | Dow Chemical Co | Acid composition for treatment of deep wells |
| US2269265A (en) * | 1939-12-14 | 1942-01-06 | Socony Vacuum Oil Co Inc | Stabilized refined petroleum product |
| US2290860A (en) * | 1940-04-26 | 1942-07-28 | Standard Oil Co | Beneficiation of lubricating oils |
| US2367264A (en) * | 1940-09-30 | 1945-01-16 | Standard Oil Co | Beneficiating lubricants, etc. |
| US2350746A (en) * | 1941-11-26 | 1944-06-06 | Socony Vacuum Oil Co Inc | Mineral oil composition |
| US2440530A (en) * | 1944-11-04 | 1948-04-27 | Shell Dev | Stabilized organic compositions |
| US2523100A (en) * | 1947-05-17 | 1950-09-19 | Standard Oil Dev Co | Mineral oil composition and additive therefor |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2982729A (en) * | 1958-04-02 | 1961-05-02 | Universal Oil Prod Co | High temperature lubricating grease containing a p, p'-diaminodiphenylether |
| US3169926A (en) * | 1961-11-29 | 1965-02-16 | Universal Oil Prod Co | Stabilization of organic substances |
| US3208944A (en) * | 1962-11-19 | 1965-09-28 | Universal Oil Prod Co | Stabilization of lubricants |
| US3240706A (en) * | 1963-01-24 | 1966-03-15 | Universal Oil Prod Co | Stabilization of organic substances |
| US3330777A (en) * | 1966-03-16 | 1967-07-11 | Universal Oil Prod Co | Stabilization of organic substances |
| US4378298A (en) * | 1981-05-12 | 1983-03-29 | Uop Inc. | Imines of 2,4-diaminodiphenyl ethers as antioxidants for lubricating oils and greases |
| US4380497A (en) * | 1981-05-12 | 1983-04-19 | Uop Inc. | Amines of alkoxydiphenyl esthers as antioxidants and lubricating oils and greases containing same |
| US4386002A (en) * | 1981-05-12 | 1983-05-31 | Uop Inc. | Imines of aminodiphenyl esthers as antioxidants and lubricating oils and greases containing same |
Also Published As
| Publication number | Publication date |
|---|---|
| ES234133A1 (es) | 1957-08-16 |
| GB819024A (en) | 1959-08-26 |
| DE1113785B (de) | 1961-09-14 |
| FR1172914A (fr) | 1959-02-17 |
| NL102710C (enrdf_load_stackoverflow) |
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