US2679480A - Indogen thickened grease composition - Google Patents
Indogen thickened grease composition Download PDFInfo
- Publication number
- US2679480A US2679480A US318322A US31832252A US2679480A US 2679480 A US2679480 A US 2679480A US 318322 A US318322 A US 318322A US 31832252 A US31832252 A US 31832252A US 2679480 A US2679480 A US 2679480A
- Authority
- US
- United States
- Prior art keywords
- lubricant
- grease
- greases
- indogen
- thickened
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000004519 grease Substances 0.000 title claims description 25
- 239000000203 mixture Substances 0.000 title description 9
- 239000000314 lubricant Substances 0.000 claims description 33
- 150000001875 compounds Chemical class 0.000 claims description 15
- 238000002844 melting Methods 0.000 claims description 8
- 230000008018 melting Effects 0.000 claims description 8
- 239000003921 oil Substances 0.000 description 20
- 229920005573 silicon-containing polymer Polymers 0.000 description 11
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 9
- 229940097275 indigo Drugs 0.000 description 9
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 9
- 239000010687 lubricating oil Substances 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 239000002562 thickening agent Substances 0.000 description 7
- CCDWGDHTPAJHOA-UHFFFAOYSA-N benzylsilicon Chemical compound [Si]CC1=CC=CC=C1 CCDWGDHTPAJHOA-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920001921 poly-methyl-phenyl-siloxane Polymers 0.000 description 5
- MLCPSWPIYHDOKG-BUHFOSPRSA-N (3e)-3-(2-oxo-1h-indol-3-ylidene)-1h-indol-2-one Chemical compound O=C\1NC2=CC=CC=C2C/1=C1/C2=CC=CC=C2NC1=O MLCPSWPIYHDOKG-BUHFOSPRSA-N 0.000 description 4
- -1 aliphatic diesters Chemical class 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- JXDYKVIHCLTXOP-UHFFFAOYSA-N isatin Chemical compound C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 3
- FGKCCLBCLJFYDJ-UHFFFAOYSA-N 3-hydroxy-3-(3-hydroxy-2-oxo-1h-indol-3-yl)-1h-indol-2-one Chemical compound O=C1NC2=CC=CC=C2C1(O)C1(O)C2=CC=CC=C2NC1=O FGKCCLBCLJFYDJ-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000010689 synthetic lubricating oil Substances 0.000 description 2
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical class Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- LIRDJALZRPAZOR-UHFFFAOYSA-N indolin-3-one Chemical compound C1=CC=C2C(=O)CNC2=C1 LIRDJALZRPAZOR-UHFFFAOYSA-N 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- LPRVNTWNHMSTPR-UHFFFAOYSA-M lithium;2-hydroxyoctadecanoate Chemical compound [Li+].CCCCCCCCCCCCCCCCC(O)C([O-])=O LPRVNTWNHMSTPR-UHFFFAOYSA-M 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 125000004957 naphthylene group Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 125000003367 polycyclic group Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C10M7/00—Solid or semi-solid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single solid or semi-solid substances
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/109—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
-
- 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/02—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/223—Five-membered rings containing nitrogen and carbon only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/02—Unspecified siloxanes; Silicones
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/041—Siloxanes with specific structure containing aliphatic substituents
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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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/042—Siloxanes with specific structure containing aromatic substituents
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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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/043—Siloxanes with specific structure containing carbon-to-carbon double bonds
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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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/044—Siloxanes with specific structure containing silicon-to-hydrogen bonds
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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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
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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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
- C10M2229/051—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon containing halogen
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/08—Resistance to extreme temperature
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
- C10N2040/13—Aircraft turbines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/08—Solids
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
Definitions
- the present invention relates to novel lubricant greases and to the method of preparing same. More particularly, it relates to novel greases comprising a lubricant vehicle thickened with certain high melting indogen compounds, specifically those melting above about 250 F. Greases of this type, particularly those wherein the lubricant vehicle comprises a silicone polymer oil, have demonstrated exceptional stability and lubricity at elevated temperatures.
- high melting indogen compounds i. e. heterocyclic compounds such as indigo, isoindigo, isatin, isatide, etc.
- heterocyclic compounds such as indigo, isoindigo, isatin, isatide, etc.
- various oleaginous vehicles may be employed to thicken various oleaginous vehicles to produce greases which are stable and display excellent lubricant properties at high temperatures.
- Compounds of this type having a melting point above about 250 F. are contemplated for use in accordance herewith.
- Silicone polymer oils are particularly preferred for use in greases employed at temperatures as high as about 450 F.
- Other lubricant vehicles either natural or synthetic, may also be thickened with such materials to produce greases particularly suited for use at temperatures between about 250 and about 400 F.
- a further object is to provide a readily producible series of greases embodying a novel class of thickening agents capable of yielding lubricants particularly suitable for use at temperatures from about 250 F. to about 450 F.
- a particular object of the present invention is to provide greases which are effective lubricants at temperatures as high as about 450 F. for substantial periods of time.
- lubricating vehicles such as silicone polymer oils, mineral lubricating oils derived from petroleum, synthetic lubricating oils such as fluorocarbons, polyalkylene glycols and their derivatives, high molecular weight esters of di-carboxylic acids, etc. and preferably the silicone polymer oils, may be thickened to grease consistency by the addition thereto of from about 10 to about and preferably from about 20 to about 50% of an indogen compound melting above about 250 F.
- R and R represent aryl or alkyl aryl radicals which are linked to the adjoining members of the heterocyclic rings by bonds disposed in ortho relation.
- These radicals may be the same or different and may be mono or poly cyclic, e.'g. phenylene, biphenylene, naphthylene, etc.
- These aryl or alkyl aryl radicals may be substituted radicals, containing various substituents such as hydroxy, carboxy, halo, nitro, etc. Examples of such compounds are indigo, iso-indigo, 3-keto-indoline, isatide, isatin, etc. It should be understood that these specific examples are enumerated for purposes of illustration and not of limitation.
- silicone polymer oils which may be employed in accordance with the present invention are those falling substantially within the lubriliquid SOz, nitrobenzene, etc.
- oils cating oil viscosity range.
- such oils have the following unit structure:
- R and B may represent substituted or: unsubstituted alkyl, aryl, alkyaryl, aryalkyl or cycloalkyl groups.
- Such compounds maybe pro-'- Jerusalemine-like methods, e. g. the hydrolysis of dialkyldichlorosilanes or. dialkyldiethoxy silanes with a suitable chain stopper, e. g. a trisubstituted monochlorosilane;
- a suitable chain stopper e. g. a trisubstituted monochlorosilane
- oils have a viscosityat 100 F. of from about 300 S. S. U. to about 1250 S. S. U.
- Suchproducts are generally colorless and inert, havea. very low volatility and undergo relatively slight. change in viscosity for a given change in tem-- perature.
- Relatively common oils of this type are dimethylsilicone polymer, phenylmethylsilicone polymer, chlorophenylmethylsilicone poly-- mer, etc., it being preferred to employ the phen-s ylinethylsilicone polymer in accordance herewith. Method of preparing such compounds are.
- a particularly desirable phenylmethylsilicone polymer the present invention is Dow-Corning 550 silicone fluid, a product of Dow-Corning, Inc., which has a viscosity at 100 F. of about 300 to about 400.
- oleaginous vehicles which may be employed herewith are, for example, mineral oils in the lubricating oil viscosity range, i. e. from about 80 S. S. U. at 100 F. to about 300 S. S. U. at210 F.
- mineral oils are preferably solvent extracted to remove substantially the low V. I. constituents, e. g. aromatics, with phenol, furfural, BB dichlorodiethylether(Chlorex), Synthetic lubri eating oils resulting from polymerization of un.
- saturated hydrocarbons or other oleaginous materials within the lubricating oil viscosity range such as high molecular weight polyoxyalkylene compounds such as polyalkylene glycols and esters thereof; aliphatic diesters of dicarboxylic acids such as the butyl, hexyl, Z-ethylhexyl,
- decyl, lauryl, etc; esters of sebacic acid, adipic acid, azelaic acid; fluorocarbons, etc.; may be thickened by the indogen compounds of the present invention to produce excellent greases.
- Greases of the present invention may be produced by any of the usual grease making techniques such as mixing thickener and oil and thenmilling the mixture in a colloid mill, 3-rollmill, etc.
- the thickener may be added to the vehicleas such or the reactants may be added and the thickener produced in situ.
- improved properties may situparted to the grease comprising asilicone vehicle by heat-treating the grease-mixture, ice.
- Prolongedv heating at such temperature may evaporate a portion of the lubricant vehicle; this loss should be replaced and then the mixture should be for use in accordance with 4 milled. If desired, the heating and readdition of vehicle may be repeated before milling.
- a typical grease of the present invention was prepared by mixing '7 grams of D0550 (phenylmethyl silicone polymer oil product of Dow- Corning, Inc. having a methyl-phenyl ratio of about 0.6 and a viscosity in the range of from about 300 to about 400 S. S. U. at 100 F.) with 15? grams of 'a" 20% (by weight) indigo paste. This'mixture was agitated in a beaker and heated while stirringuntil the temperature of the mixture was above about 300 F. The mixture was thereafter cooled and milled in a 3-roll mill. The resulting grease was smooth and had a consistency of N. L. G. I. No. 1 grade. The grease soprepared was then tested in the A. B. E. C.- Ni L. G. I. high speed high temperature bearing test. (hereinafter described in detail). At 450 and 10,000 R. P. running in cycles of 20 hours operating and 4 hours at rest, the grease lubricated the bearing for 427 hours before failure.
- D0550
- the bearingtest referred to above is a tenta-- tive one adopted by the Coordinating Research Council during the. last World War and is generally referred to as the A. B. E. C.-N. L. G. I. test. It is conducted as follows: 3 grams of grease are placed in each of two bearings disposed on the test spindle. One bearing, a special heat treated precision 204 Norma-Hoffman bear ing, is subjected to a temperature of 450 F. in an oven, the other bearing, a standard New Departure 204 bearing, is at room temperature. Temperature is determined by a thermocouple inserted .in the grease between the races of the bearing in the oven. Failure is adjudged to occur when (1) the temperature in the test bear ing reaches 470" F. or higher, (2) wattage in excess of 300% of normal wattage as required,
- the paste preparation comprising 20% indigo, referredto above, is .a commercially available product ofNational Aniline Division of Allied. Chemical and Dye Corporation.
- the paste comprises 20% of indigo by weight and 80%. of water. This material may be employed satisface as indicated, or pure indigo itself, not in paste form, may beemployed.
- a grease was. prepared by mixing 3.6 grams of indigo with 8.4 grams of.DC550 silicone oil in a beaker. The.
- smoothbuttery blue grease resulting from mil-- ling this mixture in a 3-roll mill had a consistency of an N. L. G. I. No. 0 grade.
- Greases prepared by thickening oleaginous materials such as polyalkyleneoxide compounds, diesters of dicarboxylic esters, etc., with indigo or.the like are stable at high temperatures although generally these greases are somewhat less stable thanthose prepared with silicone oil or, fluorocarbons as the lubricant vehicle. Accordingly, they aremore suitably employed in .the' range of 250 F. to about 400 F. It should be understood, in any event that while the greases of the present invention are particularly suitable for use at temperatures above 250 F., they may be employed for many purposes at lower temper-- aturesand with excellent results. These greasesmay have added thereto anti-oxidants, oiliness agents, extreme pressure additives, etc. without in any way departingfrom the scope of the present 75' invention.
- a lubricant grease comprising essentially a lubricant vehicle thickened with an amount of from about 10% to about 70% by weight of an indogen compound melting above about 250 F.
- lubricant grease of claim 1 wherein the lubricant vehicle comprises a silicone polymer oil in the lubricating viscosity range.
- lubricant grease of claim 1 wherein the lubricant vehicle comprises an acyclic ester of an aliphatic di-carboxylic acid in the lubricating oil viscosity range.
- the lubricant grease of claim 1 wherein the lubricant vehicle comprises a polyoxyalkylene compound in the lubricating oil viscosity range.
- lubricant grease of claim 1 wherein the lubricant vehicle comprises a polyfiuoro-compound in the lubricating oil viscosity range.
- a lubricant grease comprising essentially a lubricant vehicle thickened with an amount of from about 10 to about 70% by weight of indigo.
- lubricant grease of claim 7 wherein the lubricant vehicle is a silicone polymer oil in the lubricating oil viscosity range.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented May 25, 1954 INDOGEN THICKENED GREASE COMPOSITION Cecil G. Brannon, Munster, and Edward A. Swakon, Hammond, Ind., assignors to Standard Oil Company, Chicago, 111., a corporation of Indiana No Drawing. Application November 1, 1952,
Serial No.
9 Claims.
The present invention relates to novel lubricant greases and to the method of preparing same. More particularly, it relates to novel greases comprising a lubricant vehicle thickened with certain high melting indogen compounds, specifically those melting above about 250 F. Greases of this type, particularly those wherein the lubricant vehicle comprises a silicone polymer oil, have demonstrated exceptional stability and lubricity at elevated temperatures.
As lubricants are required to perform at higher and higher temperatures because of increased speeds of engines and machines, the advent of jet propulsion, atomic energy as a source of power, etc., it has become increasingly difiicult to prepare greases fulfilling the requirements of such lubricants. In attempting to provide such greases, the art has progressed from the use of petroleum lubricant vehicles thickened with metal soaps of long chain fatty acids, e. g. lithium hydroxystearate, to more thermally stable synthetic lubricating oils such as the aliphatic diesters of dicarboxylic acids, silicone polymers, etc., thickened with such soaps or inorganic materials such as silica gels, etc. The progress of thickener research has not in general, however, kept pace with the development of lubricant vehicles. And at operating temperatures as high as 400 to 450 able which will retain their consistency and lubricity for any substantial period of time.
In recent years various synthetic lubricant vehicles, e. g. the silicone polymers, fluorocarbons, etc., have been found potentially valuable for use in greases employed at very high temperatures because of their thermal stability and relatively low volatility. Unless, however, a thickener having substantially the same degree of thermal stability is available to produce a grease from such an oil, they are of little use.
In accordance with the present invention high melting indogen compounds, i. e. heterocyclic compounds such as indigo, isoindigo, isatin, isatide, etc., may be employed to thicken various oleaginous vehicles to produce greases which are stable and display excellent lubricant properties at high temperatures. Compounds of this type having a melting point above about 250 F. are contemplated for use in accordance herewith. Silicone polymer oils are particularly preferred for use in greases employed at temperatures as high as about 450 F. Other lubricant vehicles, either natural or synthetic, may also be thickened with such materials to produce greases particularly suited for use at temperatures between about 250 and about 400 F.
F. there are few if any greases avail- It is a primary object of the present invention to provide lubricant greases which are stable and give excellent lubrication at temperatures above about 250 F. A further object is to provide a readily producible series of greases embodying a novel class of thickening agents capable of yielding lubricants particularly suitable for use at temperatures from about 250 F. to about 450 F. A particular object of the present invention is to provide greases which are effective lubricants at temperatures as high as about 450 F. for substantial periods of time. These and additional objects will be apparent from the following detailed description.
We have found that lubricating vehicles such as silicone polymer oils, mineral lubricating oils derived from petroleum, synthetic lubricating oils such as fluorocarbons, polyalkylene glycols and their derivatives, high molecular weight esters of di-carboxylic acids, etc. and preferably the silicone polymer oils, may be thickened to grease consistency by the addition thereto of from about 10 to about and preferably from about 20 to about 50% of an indogen compound melting above about 250 F.
Thus, in accordance herewith, those compounds melting above about 250 F. which contain either of the structures shown empirically below are contemplated as thickening agents in the art of grease manufacture and shall be referred to broadly herein and in the appended claims as indogen compounds:
In the above formulae, R and R represent aryl or alkyl aryl radicals which are linked to the adjoining members of the heterocyclic rings by bonds disposed in ortho relation. These radicals may be the same or different and may be mono or poly cyclic, e.'g. phenylene, biphenylene, naphthylene, etc. These aryl or alkyl aryl radicals may be substituted radicals, containing various substituents such as hydroxy, carboxy, halo, nitro, etc. Examples of such compounds are indigo, iso-indigo, 3-keto-indoline, isatide, isatin, etc. It should be understood that these specific examples are enumerated for purposes of illustration and not of limitation.
The silicone polymer oils which may be employed in accordance with the present invention are those falling substantially within the lubriliquid SOz, nitrobenzene, etc.
cating oil viscosity range. In general, such oils have the following unit structure:
wherein R and B may represent substituted or: unsubstituted alkyl, aryl, alkyaryl, aryalkyl or cycloalkyl groups. Such compounds maybe pro-'- duced by well-known methods, e. g. the hydrolysis of dialkyldichlorosilanes or. dialkyldiethoxy silanes with a suitable chain stopper, e. g. a trisubstituted monochlorosilane; For purposes of the present invention, only those polymers which are high boiling liquids withinthe lubricating oil viscosity range are suitable, these-generally, possessing a viscosity at 100 F. which is within the range of from about 25 to about 3500 SZS.U. It is preferred, for purposes hereof, to employ such oils as have a viscosityat 100 F. of from about 300 S. S. U. to about 1250 S. S. U. Suchproducts are generally colorless and inert, havea. very low volatility and undergo relatively slight. change in viscosity for a given change in tem-- perature. Relatively common oils of this type are dimethylsilicone polymer, phenylmethylsilicone polymer, chlorophenylmethylsilicone poly-- mer, etc., it being preferred to employ the phen-s ylinethylsilicone polymer in accordance herewith. Method of preparing such compounds are.
taught in numerous patents, e. g. U. S. 2,410,346, U. S. 2,456,496, and in the literature suchas. Chemistry of the Silicones byRochow, page 61, et seq. A particularly desirable phenylmethylsilicone polymer the present invention is Dow-Corning 550 silicone fluid, a product of Dow-Corning, Inc., which has a viscosity at 100 F. of about 300 to about 400. S. S. U.
Other oleaginous vehicles which may be employed herewith are, for example, mineral oils in the lubricating oil viscosity range, i. e. from about 80 S. S. U. at 100 F. to about 300 S. S. U. at210 F. These mineral oils are preferably solvent extracted to remove substantially the low V. I. constituents, e. g. aromatics, with phenol, furfural, BB dichlorodiethylether(Chlorex), Synthetic lubri eating oils resulting from polymerization of un. saturated hydrocarbons or other oleaginous materials within the lubricating oil viscosity rangesuch as high molecular weight polyoxyalkylene compounds such as polyalkylene glycols and esters thereof; aliphatic diesters of dicarboxylic acids such as the butyl, hexyl, Z-ethylhexyl,
decyl, lauryl, etc; esters of sebacic acid, adipic acid, azelaic acid; fluorocarbons, etc.; may be thickened by the indogen compounds of the present invention to produce excellent greases.
Greases of the present invention may be produced by any of the usual grease making techniques such as mixing thickener and oil and thenmilling the mixture in a colloid mill, 3-rollmill, etc. The thickener may be added to the vehicleas such or the reactants may be added and the thickener produced in situ. As a-step in anyof the usual techniques improved properties may beimparted to the grease comprising asilicone vehicle by heat-treating the grease-mixture, ice.
subjecting same to a temperature of about 450 F. for at least about half an hour and preferably longer, e. g. from about 1 to 20 hours. Prolongedv heating at such temperature may evaporate a portion of the lubricant vehicle; this loss should be replaced and then the mixture should be for use in accordance with 4 milled. If desired, the heating and readdition of vehicle may be repeated before milling.
A typical grease of the present invention was prepared by mixing '7 grams of D0550 (phenylmethyl silicone polymer oil product of Dow- Corning, Inc. having a methyl-phenyl ratio of about 0.6 and a viscosity in the range of from about 300 to about 400 S. S. U. at 100 F.) with 15? grams of 'a" 20% (by weight) indigo paste. This'mixture was agitated in a beaker and heated while stirringuntil the temperature of the mixture was above about 300 F. The mixture was thereafter cooled and milled in a 3-roll mill. The resulting grease was smooth and had a consistency of N. L. G. I. No. 1 grade. The grease soprepared was then tested in the A. B. E. C.- Ni L. G. I. high speed high temperature bearing test. (hereinafter described in detail). At 450 and 10,000 R. P. running in cycles of 20 hours operating and 4 hours at rest, the grease lubricated the bearing for 427 hours before failure.
The bearingtest referred to above is a tenta-- tive one adopted by the Coordinating Research Council during the. last World War and is generally referred to as the A. B. E. C.-N. L. G. I. test. It is conducted as follows: 3 grams of grease are placed in each of two bearings disposed on the test spindle. One bearing, a special heat treated precision 204 Norma-Hoffman bear ing, is subjected to a temperature of 450 F. in an oven, the other bearing, a standard New Departure 204 bearing, is at room temperature. Temperature is determined by a thermocouple inserted .in the grease between the races of the bearing in the oven. Failure is adjudged to occur when (1) the temperature in the test bear ing reaches 470" F. or higher, (2) wattage in excess of 300% of normal wattage as required,
' 012(3) thebearing does not turn over at the be- 'torily in the preparation of greases,
ginning of a test cycle (the test is conducted incycles of, 20 hours operating and 4 hours at rest).
The paste preparation comprising 20% indigo, referredto above, is .a commercially available product ofNational Aniline Division of Allied. Chemical and Dye Corporation. The paste comprises 20% of indigo by weight and 80%. of water. This material may be employed satisface as indicated, or pure indigo itself, not in paste form, may beemployed. Thus, for example, a grease was. prepared by mixing 3.6 grams of indigo with 8.4 grams of.DC550 silicone oil in a beaker. The.
smoothbuttery blue grease resulting from mil-- ling this mixture in a 3-roll mill had a consistency of an N. L. G. I. No. 0 grade.
Greases prepared by thickening oleaginous materials such as polyalkyleneoxide compounds, diesters of dicarboxylic esters, etc., with indigo or.the like are stable at high temperatures although generally these greases are somewhat less stable thanthose prepared with silicone oil or, fluorocarbons as the lubricant vehicle. Accordingly, they aremore suitably employed in .the' range of 250 F. to about 400 F. It should be understood, in any event that while the greases of the present invention are particularly suitable for use at temperatures above 250 F., they may be employed for many purposes at lower temper-- aturesand with excellent results. These greasesmay have added thereto anti-oxidants, oiliness agents, extreme pressure additives, etc. without in any way departingfrom the scope of the present 75' invention.
Having thus described our invention, what we claim as novel and desire to protect by Letters Patent is defined by the following claims:
1. A lubricant grease comprising essentially a lubricant vehicle thickened with an amount of from about 10% to about 70% by weight of an indogen compound melting above about 250 F.
2. The lubricant grease of claim 1 wherein the lubricant vehicle comprises a silicone polymer oil in the lubricating viscosity range.
3. The lubricant grease of claim 2 wherein the silicone polymer oil comprises a phenyl-methyl silicone polymer oil in the lubricating oil viscosity range.
4. The lubricant grease of claim 1 wherein the lubricant vehicle comprises an acyclic ester of an aliphatic di-carboxylic acid in the lubricating oil viscosity range.
5. The lubricant grease of claim 1 wherein the lubricant vehicle comprises a polyoxyalkylene compound in the lubricating oil viscosity range.
6. The lubricant grease of claim 1 wherein the lubricant vehicle comprises a polyfiuoro-compound in the lubricating oil viscosity range.
7. A lubricant grease comprising essentially a lubricant vehicle thickened with an amount of from about 10 to about 70% by weight of indigo.
8. The lubricant grease of claim 7 wherein the lubricant vehicle is a silicone polymer oil in the lubricating oil viscosity range.
9. The lubricant grease of claim. 8 wherein the silicone polymer oil is a phenyl-methyl silicone polymer oil.
No references cited.
Claims (1)
1. A LUBRICANT GREASE COMPRISING ESSENTIALLY A LUBRICANT VEHICLE THICKENED WITH AN AMOUNT OF FROM ABOUT 10% TO ABOUT 70% BY WEIGHT OF AN INDOGEN COMPOUND MELTING ABOVE ABOUT 250* F.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US318322A US2679480A (en) | 1952-11-01 | 1952-11-01 | Indogen thickened grease composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US318322A US2679480A (en) | 1952-11-01 | 1952-11-01 | Indogen thickened grease composition |
Publications (1)
Publication Number | Publication Date |
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US2679480A true US2679480A (en) | 1954-05-25 |
Family
ID=23237680
Family Applications (1)
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US318322A Expired - Lifetime US2679480A (en) | 1952-11-01 | 1952-11-01 | Indogen thickened grease composition |
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2791560A (en) * | 1954-04-14 | 1957-05-07 | Texas Co | Lubricating grease thickened with a sodium or lithium soap and indigo |
US2915470A (en) * | 1957-12-16 | 1959-12-01 | Shell Dev | Grease manufacturing process for pigment or dye gelled oils |
US2940928A (en) * | 1958-04-28 | 1960-06-14 | Shell Oil Co | Dye-clay grease composition and manufacturing process therefor |
US2978413A (en) * | 1958-12-19 | 1961-04-04 | Texaco Inc | Lubricating oils thickened to a grease consistency with cuprous n, n'-diarylamidine compounds |
US3010904A (en) * | 1958-12-23 | 1961-11-28 | Texaco Inc | Lubricating greases thickened with dioxazine carbazole compounds |
US3010905A (en) * | 1959-07-10 | 1961-11-28 | Texaco Inc | Lubricating greases thickened with nitrophenylazo naphthol compounds |
US3013972A (en) * | 1959-08-06 | 1961-12-19 | Texaco Inc | Greases thickened with polyvalent metal salts of 2(2-hydroxy-3-carboxy-1-naphthylazo)benzenesulfonic acids |
US3102860A (en) * | 1960-08-31 | 1963-09-03 | Socony Mobil Oil Co Inc | Naphthalic imidazole grease |
US3126341A (en) * | 1960-07-29 | 1964-03-24 | Certificate of correction |
-
1952
- 1952-11-01 US US318322A patent/US2679480A/en not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
---|
None * |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2791560A (en) * | 1954-04-14 | 1957-05-07 | Texas Co | Lubricating grease thickened with a sodium or lithium soap and indigo |
US2915470A (en) * | 1957-12-16 | 1959-12-01 | Shell Dev | Grease manufacturing process for pigment or dye gelled oils |
US2940928A (en) * | 1958-04-28 | 1960-06-14 | Shell Oil Co | Dye-clay grease composition and manufacturing process therefor |
US2978413A (en) * | 1958-12-19 | 1961-04-04 | Texaco Inc | Lubricating oils thickened to a grease consistency with cuprous n, n'-diarylamidine compounds |
US3010904A (en) * | 1958-12-23 | 1961-11-28 | Texaco Inc | Lubricating greases thickened with dioxazine carbazole compounds |
US3010905A (en) * | 1959-07-10 | 1961-11-28 | Texaco Inc | Lubricating greases thickened with nitrophenylazo naphthol compounds |
US3013972A (en) * | 1959-08-06 | 1961-12-19 | Texaco Inc | Greases thickened with polyvalent metal salts of 2(2-hydroxy-3-carboxy-1-naphthylazo)benzenesulfonic acids |
US3126341A (en) * | 1960-07-29 | 1964-03-24 | Certificate of correction | |
US3102860A (en) * | 1960-08-31 | 1963-09-03 | Socony Mobil Oil Co Inc | Naphthalic imidazole grease |
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