US2620301A - Grease compositions - Google Patents
Grease compositions Download PDFInfo
- Publication number
- US2620301A US2620301A US200110A US20011050A US2620301A US 2620301 A US2620301 A US 2620301A US 200110 A US200110 A US 200110A US 20011050 A US20011050 A US 20011050A US 2620301 A US2620301 A US 2620301A
- Authority
- US
- United States
- Prior art keywords
- oil
- grease
- salt
- guanidine
- preferentially
- 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 claims description 25
- 239000004215 Carbon black (E152) Substances 0.000 claims description 14
- 229930195733 hydrocarbon Natural products 0.000 claims description 14
- 150000002430 hydrocarbons Chemical class 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 10
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 7
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical class NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 2
- 239000003921 oil Substances 0.000 description 36
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 17
- 239000003208 petroleum Substances 0.000 description 17
- 150000003839 salts Chemical class 0.000 description 11
- 150000003460 sulfonic acids Chemical class 0.000 description 11
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 9
- 241000158728 Meliaceae Species 0.000 description 9
- -1 for example Chemical class 0.000 description 8
- 150000002357 guanidines Chemical class 0.000 description 8
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 239000000344 soap Substances 0.000 description 5
- 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 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 239000000314 lubricant Substances 0.000 description 4
- 230000002441 reversible effect Effects 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- ZZTURJAZCMUWEP-UHFFFAOYSA-N diaminomethylideneazanium;hydrogen sulfate Chemical compound NC(N)=N.OS(O)(=O)=O ZZTURJAZCMUWEP-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- DXTIKTAIYCJTII-UHFFFAOYSA-N guanidine acetate Chemical compound CC([O-])=O.NC([NH3+])=N DXTIKTAIYCJTII-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 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
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- HRKQOINLCJTGBK-UHFFFAOYSA-N dihydroxidosulfur Chemical compound OSO HRKQOINLCJTGBK-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 239000010735 electrical insulating oil Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229960004198 guanidine Drugs 0.000 description 1
- 229960000789 guanidine hydrochloride Drugs 0.000 description 1
- PJJJBBJSCAKJQF-UHFFFAOYSA-N guanidinium chloride Chemical compound [Cl-].NC(N)=[NH2+] PJJJBBJSCAKJQF-UHFFFAOYSA-N 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 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
- 239000003760 tallow Substances 0.000 description 1
- 239000010723 turbine oil Substances 0.000 description 1
- 238000005406 washing Methods 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
- 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
- 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
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M2211/022—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
-
- 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
- C10M2211/06—Perfluorinated compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/10—Amides of carbonic or haloformic 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/084—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; 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
- 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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- 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
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
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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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
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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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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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
- C10N2040/02—Bearings
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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—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
Definitions
- This invention relates to improvements in lubricant greases, and more particularly relates to stable, thermally reversible lubricant greases.
- Another object of the present invention is to provide an improved stable grease composition. Another object of the invention is to provide a thermally reversible grease. Other objects and advantages will become apparent from the following description thereof.
- Greases of the present invention comprise essentially a normally liquid oleagincus compound, preferably a hydrocarbon oil, and from about 0.1% to about 15%, and preferably from about 0.5% to about 5%, of a guanidine salt, such as for example, guanidine carbonate, guanidine acetate, guanidine sulfate, guanidine hydrochloride, etc., and from about 1% to about 50%, and preferably from about 5% to about of a hydrocarbon oil sulfonate, preferably a preferentially oil-soluble petroleum sulfonate.
- a guanidine salt such as for example, guanidine carbonate, guanidine acetate, guanidine sulfate, guanidine hydrochloride, etc.
- a hydrocarbon oil sulfonate preferably a preferentially oil-soluble petroleum sulfonate.
- hydrocarbon oil sulfonic acids which can be used to produce sulfonates of this invention are those obtained in the treatment of hydrocarbon oils, such as mineral or petroleum oils with strong sulfuric acid, such as concentrated or fuming sulfuric acid.
- hydrocarbon oils such as mineral or petroleum oils with strong sulfuric acid, such as concentrated or fuming sulfuric acid.
- the petroleum oils are treated successively with a number of portions of concentrated sulfuric acid (1. e. above about 95% strength) or fuming sulfuric acid.
- a variety of sulfur-containing compounds are formed by the chemical reaction of the sulfuric acid upon the oil, including sulfonic acids, organic esters of sulfuric acid, partial esters of sulfuric acid, etc.
- mahogany acids Because of the characteristic mahogany color of these preferentially oil-soluble sulfonic acids, they are known in the petroleum art as mahogany acids.
- the salts of such mahogany 2 acids can be obtained by neutralizing the acidtreated oil with basic alkali metal or alkaline earth compound to form sulfonates which are then extracted from the oil by treatment with 50% to aqueous alcohol solutions or other suitable means.
- alkali metal salts such as sodium, potassium and lithium
- alkaline earth salts such as calcium, barium, strontium, etc.
- the heavy metal salts of such acids can also be used.
- the preferentially oil-soluble petroleum sulfonic acids have molecular weights ranging from about 350 to about 525. While any of these sulfonic acids can be used, we prefer to use those having molecular weights ranging from about 400 to about 500, particularly those having molecular Weights in the range of about 430 to 450, and 4'70 to 500.
- Greases of the type described can be readily prepared by stirring a mixture of the guanidine salt, sulfonate and hydrocarbon oil at a temperature of from about 220 F. to about 350 F. to effeet a solution of the sulfonate in the oil, and then permitting the mixture to cool to room temperature.
- the liquid vehicle of the grease can be any liquid lubricant, either natural or synthetic, usually having Saybolt Universal viscosities in the range of from about 65 seconds at F. to about 400 seconds at 210 F., capable of being used in grease compositions.
- examples of such vehicles are hydrocarbon oils, 1. e., petroleum oils, and synthetic hydrocarbon lubricating oils, such as for example, those obtained by the polymerization of olefins and oils in the lubricating oil range obtained in the Fischer-Tropsch process.
- Other suitable synthetic oleaginous compounds are aliphatic dicarboxylic acid esters of the type disclosed in U. S. Patent 2,430,222, the esters of dihydroxy thioether, such as are disclosed in U. S. Patent 2,451,895, silicone polymers and the monohydroxy, 1,2 polyoxypropylene aliphatic monoethers of the type described in U. S. Patent 2,488,644, etc.
- greases prepared in accordance with the present invention may contain other constituents such as for example E. P. agents, for example, chlorine and/or sulfur-containing compounds, pourpoint depressors, for example, condensation products of the type described in U. S. Patents 1,963,917 and 1,963,918, oiliness agents, rust inhibitors, antioxidants, the alkali metal and/or alkaline earth soap of high molecular weight fats and fatty acids, for example, tallow, lard, palmitic acid, stearic acid, oleic acid, animal fatty acids, etc.
- E. P. agents for example, chlorine and/or sulfur-containing compounds
- pourpoint depressors for example, condensation products of the type described in U. S. Patents 1,963,917 and 1,963,918, oiliness agents, rust inhibitors, antioxidants, the alkali metal and/or alkaline earth soap of high molecular weight fats and fatty acids, for example, tallow, lard, palmitic acid, ste
- Example I The product of Example I was prepared by heating a mixture of the mahogany soap and oil to a temperature of about 300350 F., adding the guanidine carbonate and cooling to room temperature.
- the grease obtained upon cooling was a thermally reversibl unctuous clear mechanically stable product, water resistant, and did not leak oil.
- the product had an A. S. T. M. drop point of 300 F. and an A. S. T. M. penetration at 77 F. of 247.
- Example 11 The product of Example 11 was prepared by heating the mixture of guanidine carbonate, mahogany soap and oil at a temperature of 300 F. for thirty minutes with agitation. Upon cooling, a thermally reversible grease of smooth structure was obtained.
- the grease had an A. S. T. M. drop point of 290 F., and A. S. T. M. un- Worked penetration of 290 at 77 F., and a worked penetration of 249.
- the grease showed no leakage at 230 F. after twenty-four hours exposure in a cone-shaped Wire gauge, and had a water absorption (Navy) of 95%.
- Greases of the present invention find application as a multi-purpose automotive grease, including stearing gear grease, including ball bearing lubricants, as washing machine lubricants, etc. Furthermore, because of their property of being thermally reversible, such products can be used in such services where cup greases are not satisfactory.
- Grease compositions containing a mixture of a preferentially oil-insoluble guanidine sulfonate and a preferentially oil-soluble sulfonate is claimed in the co-pending application of G. T. McLeod et 2.1. Serial No. 192,824 filed October 28, 1950.
- a grease composition comprising essentially a major proportion of a normally liquid oleaginous material, from about 0.1% to about 15% of a water-soluble guanidine salt of a low molecular weight acid, and from about 1% to about 50% of a preferentially oil-soluble hydrocarbon oil sulfonate.
- a liquid composition comprising essentially a major proportion of a normally liquid hydrocarbon oil, from about 0.1% to about 15% of a water-soluble guanidine salt of a low molecular weight acid, and from about 1% to about 50% of a salt of a preferentially oil-soluble petroleum sulfonic acid.
- a grease composition comprising essentially a major proportion of a normally liquid hydrocarbon oil, from about 0.5% to about 5% of a guanidine carbonate, and from about 5% to about 20% of a sodium salt of preferentially oil-soluble petroleum sulfonic acid having a molecular weight of about 350 to about 525.
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- Chemical & Material Sciences (AREA)
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Description
Patented Dec. 2, 1952 GREASE COMPOSITIONS Gordon D. McLeod, Hammond, Ind., assignor to Standard Oil Company, Chicago, III., a corporation of Indiana No Drawing. Application December 9, 1950,
' Serial No. 200,110
12 Claims. 1
This invention relates to improvements in lubricant greases, and more particularly relates to stable, thermally reversible lubricant greases.
It is an object of the present invention to provide an improved stable grease composition. Another object of the invention is to provide a thermally reversible grease. Other objects and advantages will become apparent from the following description thereof.
Greases of the present invention comprise essentially a normally liquid oleagincus compound, preferably a hydrocarbon oil, and from about 0.1% to about 15%, and preferably from about 0.5% to about 5%, of a guanidine salt, such as for example, guanidine carbonate, guanidine acetate, guanidine sulfate, guanidine hydrochloride, etc., and from about 1% to about 50%, and preferably from about 5% to about of a hydrocarbon oil sulfonate, preferably a preferentially oil-soluble petroleum sulfonate.
The hydrocarbon oil sulfonic acids which can be used to produce sulfonates of this invention are those obtained in the treatment of hydrocarbon oils, such as mineral or petroleum oils with strong sulfuric acid, such as concentrated or fuming sulfuric acid. In the treatment of petroleum oils to obtain highly refined products of the type of electrical insulating oils, turbine oils, technical white oils and medicinal white oils, etc., the petroleum oils are treated successively with a number of portions of concentrated sulfuric acid (1. e. above about 95% strength) or fuming sulfuric acid. A variety of sulfur-containing compounds are formed by the chemical reaction of the sulfuric acid upon the oil, including sulfonic acids, organic esters of sulfuric acid, partial esters of sulfuric acid, etc. Most of these compounds are relatively insoluble in the oil under the treated conditions and separate from the oil together with the unreacted sulfuric acid, as a sludge, which is separated from the oil after each acid treatment. The sulfuric acid is usually added in dumps of about one-half pound per gallon of oil, the total quantity of acid treated depending upon the oil treated and the desired final product. Usually, from about three pounds to about nine pounds of sulfuric acid er gallon of oil are used. Some of the sulfonic acids resulting from the treatment of the oil with sulfuric acid are preferentially oil-soluble and remain in the oil layer after removal of the acid sludge. Because of the characteristic mahogany color of these preferentially oil-soluble sulfonic acids, they are known in the petroleum art as mahogany acids. The salts of such mahogany 2 acids can be obtained by neutralizing the acidtreated oil with basic alkali metal or alkaline earth compound to form sulfonates which are then extracted from the oil by treatment with 50% to aqueous alcohol solutions or other suitable means.
The alkali metal salts, such as sodium, potassium and lithium, and the alkaline earth salts, such as calcium, barium, strontium, etc., of preferentially oil-soluble petroleum sulfonic acids are preferred, although the heavy metal salts of such acids can also be used.
The preferentially oil-soluble petroleum sulfonic acids have molecular weights ranging from about 350 to about 525. While any of these sulfonic acids can be used, we prefer to use those having molecular weights ranging from about 400 to about 500, particularly those having molecular Weights in the range of about 430 to 450, and 4'70 to 500. In preparing the sulfonate from the petroleum sulfonic acids, We can use substantially oil-free sulfonic acids, although for practical purposes blends of oil and sulfonic acids can be used. Usually, the sulfonic acids are recovered as blends of about 40-50% sulfonic acid in hydrocarbon oil.
Greases of the type described can be readily prepared by stirring a mixture of the guanidine salt, sulfonate and hydrocarbon oil at a temperature of from about 220 F. to about 350 F. to effeet a solution of the sulfonate in the oil, and then permitting the mixture to cool to room temperature.
The liquid vehicle of the grease can be any liquid lubricant, either natural or synthetic, usually having Saybolt Universal viscosities in the range of from about 65 seconds at F. to about 400 seconds at 210 F., capable of being used in grease compositions. Examples of such vehicles are hydrocarbon oils, 1. e., petroleum oils, and synthetic hydrocarbon lubricating oils, such as for example, those obtained by the polymerization of olefins and oils in the lubricating oil range obtained in the Fischer-Tropsch process. Other suitable synthetic oleaginous compounds are aliphatic dicarboxylic acid esters of the type disclosed in U. S. Patent 2,430,222, the esters of dihydroxy thioether, such as are disclosed in U. S. Patent 2,451,895, silicone polymers and the monohydroxy, 1,2 polyoxypropylene aliphatic monoethers of the type described in U. S. Patent 2,488,644, etc.
The type of oil and the viscosity selected will depend upon the intended use and service for the grease. In addition to the guanidine salt, greases prepared in accordance with the present invention may contain other constituents such as for example E. P. agents, for example, chlorine and/or sulfur-containing compounds, pourpoint depressors, for example, condensation products of the type described in U. S. Patents 1,963,917 and 1,963,918, oiliness agents, rust inhibitors, antioxidants, the alkali metal and/or alkaline earth soap of high molecular weight fats and fatty acids, for example, tallow, lard, palmitic acid, stearic acid, oleic acid, animal fatty acids, etc.
The following specific examples further illustrate the present invention. It is to be understood that the examples are for illustrative purposes only and should not be regarded as limiting the scope of the invention.
Example I Per cent Guanidine carbonate 2.2 Sodium mahogany soap 10.0
Hydrocarbon 011 (S. U. S. at 100 F.-210215) 87.8
Prepared from mahogany acids having a molecular weight of 430-450.
Example II Per cent Guanidine carbonate 2.8
Sodium mahogany soap 8.7 Hydrocarbon oil (6. U. S. at 100 F.
Prepared from mahogany acids having a molecular weight of 470-500.
The product of Example I was prepared by heating a mixture of the mahogany soap and oil to a temperature of about 300350 F., adding the guanidine carbonate and cooling to room temperature. The grease obtained upon cooling was a thermally reversibl unctuous clear mechanically stable product, water resistant, and did not leak oil. The product had an A. S. T. M. drop point of 300 F. and an A. S. T. M. penetration at 77 F. of 247.
The product of Example 11 was prepared by heating the mixture of guanidine carbonate, mahogany soap and oil at a temperature of 300 F. for thirty minutes with agitation. Upon cooling, a thermally reversible grease of smooth structure was obtained. The grease had an A. S. T. M. drop point of 290 F., and A. S. T. M. un- Worked penetration of 290 at 77 F., and a worked penetration of 249. The grease showed no leakage at 230 F. after twenty-four hours exposure in a cone-shaped Wire gauge, and had a water absorption (Navy) of 95%.
Greases of the present invention find application as a multi-purpose automotive grease, including stearing gear grease, including ball bearing lubricants, as washing machine lubricants, etc. Furthermore, because of their property of being thermally reversible, such products can be used in such services where cup greases are not satisfactory.
Percentages given herein and in the appended claims are weight percentages unless otherwise specified.
Grease compositions containing a mixture of a preferentially oil-insoluble guanidine sulfonate and a preferentially oil-soluble sulfonate is claimed in the co-pending application of G. T. McLeod et 2.1. Serial No. 192,824 filed October 28, 1950.
While the present invention has been described by reference to specific embodiments thereof,
4 these have been given by way of illustration and the invention is not to be limited thereby but includes within its scope such modifications as come within the spirit of the appended claims.
I claim:
1. A grease composition comprising essentially a major proportion of a normally liquid oleaginous material, from about 0.1% to about 15% of a water-soluble guanidine salt of a low molecular weight acid, and from about 1% to about 50% of a preferentially oil-soluble hydrocarbon oil sulfonate.
2. A liquid composition comprising essentially a major proportion of a normally liquid hydrocarbon oil, from about 0.1% to about 15% of a water-soluble guanidine salt of a low molecular weight acid, and from about 1% to about 50% of a salt of a preferentially oil-soluble petroleum sulfonic acid.
3. A composition as described in claim 2 in which the guanidine salt is guanidine carbonate.
4. A grease composition described in claim 2 in which the guanidine salt is guanidine acetate.
5. A grease composition as described in claim 2 in which the guanidine salt is guanidine sulfate.
6. A grease composition as described in claim 2 in which the salt of the preferentially oilsoluble petroleum sulfonic acid is an alkali metal salt.
7. A grease composition as described in claim 2 in which the salt of the preferentially oilsoluble petroleum sulfonic acid is sodium.
8. A grease composition as described in claim 2 in which the salt of the preferentially oilsoluble petroleum sulfonic acid is lithium.
9. A grease composition as described in claim 2 in which the salt of the preferentially oilsoluble petroleum sulfonic acid is an alkaline earth salt.
10. A grease composition as described in claim 2 in which the salt of the preferentially oilsoluble petroleum sulfonic acid is calcium.
11. A grease composition as described in claim 2 in which the salt of the preferentially oilsoluble petroleum sulfonic acid is barium.
12. A grease composition comprising essentially a major proportion of a normally liquid hydrocarbon oil, from about 0.5% to about 5% of a guanidine carbonate, and from about 5% to about 20% of a sodium salt of preferentially oil-soluble petroleum sulfonic acid having a molecular weight of about 350 to about 525.
GORDON D. MCLEOD.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS
Claims (1)
1. A GREASE COMPOSITION COMPRISING ESSENTIALLY A MAJOR PROPORTION OF A NORMALLY LIQUID OLEAGINOUS MATERIAL, FROM ABOUT 0.1% TO ABOUT 15% OF A WATER-SOLUBLE GUANIDINE SALT OF A LOW MOLECULAR WEIGHT ACID, AND FROM ABOUT 1% TO ABOUT 50% OF A PREFERENTIALLY OIL-SOLUBLE HYDROCARBON OIL SULFONATE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US200110A US2620301A (en) | 1950-12-09 | 1950-12-09 | Grease compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US200110A US2620301A (en) | 1950-12-09 | 1950-12-09 | Grease compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2620301A true US2620301A (en) | 1952-12-02 |
Family
ID=22740372
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US200110A Expired - Lifetime US2620301A (en) | 1950-12-09 | 1950-12-09 | Grease compositions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2620301A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE961283C (en) * | 1953-10-20 | 1957-04-04 | Exxon Research Engineering Co | Process for stabilizing the low temperature viscosity of synthetic lubricating oils |
| US2987477A (en) * | 1958-12-29 | 1961-06-06 | Texaco Inc | Lubricating greases containing metal salts of nu-alkanoyl-sulfanilic acids |
| US4163800A (en) * | 1977-08-17 | 1979-08-07 | The Procter & Gamble Company | Topical composition and treatment of skin lesions therewith |
| US4246285A (en) * | 1975-10-20 | 1981-01-20 | The Procter & Gamble Company | Skin conditioning compositions containing guanidine inorganic salts |
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| US2061601A (en) * | 1929-06-20 | 1936-11-24 | Standard Oil Dev Co | Process of preparing alcohol-amine mineral oil sulphonates |
| US2209169A (en) * | 1939-03-25 | 1940-07-23 | Standard Oil Dev Co | Process for the preparation of oil solutions of organic sulphonates |
| US2223935A (en) * | 1939-04-01 | 1940-12-03 | American Cyanamid Co | Amidine salts of alkyl naphthalene sulphonic acids |
| US2270755A (en) * | 1940-12-21 | 1942-01-20 | American Cyanamid Co | Sulphonic acids of amidines |
| US2345388A (en) * | 1941-04-26 | 1944-03-28 | American Cyanamid Co | Substituted guanidine salts of alkyl phosphoric acids and their preparation |
| US2372588A (en) * | 1940-06-19 | 1945-03-27 | Shell Dev | Compounded mineral oil |
| US2444970A (en) * | 1944-12-30 | 1948-07-13 | Standard Oil Dev Co | Grease compositions |
| US2446867A (en) * | 1944-04-01 | 1948-08-10 | Libbey Owens Ford Glass Co | Urea-formaldehyde composition |
| US2467118A (en) * | 1945-01-06 | 1949-04-12 | Standard Oil Dev Co | Complex from a polyvalent metal petroleum sulfonate, a process of making it, and a lubricating oil containing it |
| US2473112A (en) * | 1946-04-03 | 1949-06-14 | Boots Pure Drug Co Ltd | Preparation of sulfonic acid salts of diguanides |
| US2535101A (en) * | 1948-03-18 | 1950-12-26 | Standard Oil Dev Co | Sulfonate base lubricating grease |
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- 1950-12-09 US US200110A patent/US2620301A/en not_active Expired - Lifetime
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2061601A (en) * | 1929-06-20 | 1936-11-24 | Standard Oil Dev Co | Process of preparing alcohol-amine mineral oil sulphonates |
| US2209169A (en) * | 1939-03-25 | 1940-07-23 | Standard Oil Dev Co | Process for the preparation of oil solutions of organic sulphonates |
| US2223935A (en) * | 1939-04-01 | 1940-12-03 | American Cyanamid Co | Amidine salts of alkyl naphthalene sulphonic acids |
| US2372588A (en) * | 1940-06-19 | 1945-03-27 | Shell Dev | Compounded mineral oil |
| US2270755A (en) * | 1940-12-21 | 1942-01-20 | American Cyanamid Co | Sulphonic acids of amidines |
| US2345388A (en) * | 1941-04-26 | 1944-03-28 | American Cyanamid Co | Substituted guanidine salts of alkyl phosphoric acids and their preparation |
| US2446867A (en) * | 1944-04-01 | 1948-08-10 | Libbey Owens Ford Glass Co | Urea-formaldehyde composition |
| US2444970A (en) * | 1944-12-30 | 1948-07-13 | Standard Oil Dev Co | Grease compositions |
| US2467118A (en) * | 1945-01-06 | 1949-04-12 | Standard Oil Dev Co | Complex from a polyvalent metal petroleum sulfonate, a process of making it, and a lubricating oil containing it |
| US2473112A (en) * | 1946-04-03 | 1949-06-14 | Boots Pure Drug Co Ltd | Preparation of sulfonic acid salts of diguanides |
| US2535101A (en) * | 1948-03-18 | 1950-12-26 | Standard Oil Dev Co | Sulfonate base lubricating grease |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE961283C (en) * | 1953-10-20 | 1957-04-04 | Exxon Research Engineering Co | Process for stabilizing the low temperature viscosity of synthetic lubricating oils |
| US2987477A (en) * | 1958-12-29 | 1961-06-06 | Texaco Inc | Lubricating greases containing metal salts of nu-alkanoyl-sulfanilic acids |
| US4246285A (en) * | 1975-10-20 | 1981-01-20 | The Procter & Gamble Company | Skin conditioning compositions containing guanidine inorganic salts |
| US4163800A (en) * | 1977-08-17 | 1979-08-07 | The Procter & Gamble Company | Topical composition and treatment of skin lesions therewith |
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