US2908645A - Blended lithium calcium base grease - Google Patents

Blended lithium calcium base grease Download PDF

Info

Publication number
US2908645A
US2908645A US504659A US50465955A US2908645A US 2908645 A US2908645 A US 2908645A US 504659 A US504659 A US 504659A US 50465955 A US50465955 A US 50465955A US 2908645 A US2908645 A US 2908645A
Authority
US
United States
Prior art keywords
grease
acids
lithium
molecular weight
component
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
Application number
US504659A
Inventor
Arnold J Morway
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority to NL104990D priority Critical patent/NL104990C/xx
Priority to BE546805D priority patent/BE546805A/xx
Application filed by Exxon Research and Engineering Co filed Critical Exxon Research and Engineering Co
Priority to US504659A priority patent/US2908645A/en
Priority to GB9885/56A priority patent/GB793484A/en
Priority to FR1152678D priority patent/FR1152678A/en
Priority to DEE12287A priority patent/DE1064667B/en
Application granted granted Critical
Publication of US2908645A publication Critical patent/US2908645A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M5/00Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/022Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/122Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/123Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/124Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms containing hydroxy groups; Ethers thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/141Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings monocarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/142Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings polycarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/144Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/146Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings having carboxyl groups bound to carbon atoms of six-membeered aromatic rings having a hydrocarbon substituent of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/22Acids obtained from polymerised unsaturated acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/24Epoxidised acids; Ester derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/286Esters of polymerised unsaturated acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/287Partial esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/30Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/30Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids
    • C10M2207/302Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids derived from the combination of monocarboxylic acids, dicarboxylic acids and dihydroxy compounds only and having no free hydroxy or carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/34Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • C10M2207/404Fatty vegetable or animal oils obtained from genetically modified species
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
    • C10M2215/065Phenyl-Naphthyl amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/102Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon only in the ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • C10M2219/106Thiadiazoles
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00Organic 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
    • C10M2229/02Unspecified siloxanes; Silicones
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00Organic 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
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/05Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/02Groups 1 or 11
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • This invention relates to improved lubricating grease compositions having outstanding lubricating life and water resistance characteristics. More particularly, the invention "pertains to blends of separate grease components to form' greases having excellent water emulsion stability and long lubrication service.
  • the invention in brief compass, relates to lubricating grease compositions comprising a blend of two component greases, one component being a lubricating oil thickened to grease consistency with an organo-metallic soap-salt or mixed salt complex, having a high combined but active metal content, and the other component being a lithium soap thickened grease.
  • These two-component greases areimade separately and then blended togetherby thorough mixing or by the use of a suitable homogenizer or grease mill.
  • organo-metallic complexes having high metal content as grease thickeners has recently been suggested.
  • these complex thickeners have been prepared from the metal salts of low molecular weight carboxylic acids in combination with metal soaps ofhigh molecular weight carboxylic acids, metal salts of intermediate molecular weight carboxylic acids, or metal salts of medium molecular weight carboxylioacids 'and metal soaps of high molecular weight ca'rboxylicacids.
  • the metal constituents of the complex thickeners have usually been selected from the 'divalent metals, especially the alkaline earth metals. Calcium is particularly preferred.
  • Greases containing these complex thickeners have been found to have outstanding extreme pressure properties and long lubricating lives, but they tend to form fluid emulsions when water is churned into them. f
  • lithium soaps in grease-making is well known in theart.
  • Such lithium soap type thickeners have been prepared from the conventional soap-forming high molecular weight carboxylic acids, including their hydroxy derivatives and esters thereof.
  • Lithium-containing grease thickeners have also been prepared from mixtures of lithium and calcium soaps of high; molecular Weight fatty acids. Greases thickened with these lithiumcontaining soaps, such asthe lithium soap of hydroxy stearic acid, haveexcellent water resistance but notably poor lubricating lives.
  • carbon atoms per molecule between the high and medium molecular weight carboxylic acid is at least 7, preferably about 7 to 15.
  • the high molecular Weight carboxylic acids useful for preparing the complex thickeners described above are those saturated and unsaturated, grease-making fatty acids thatare commonly known to the art. In general, these fatty acids have from about 12 to 30 carbon atoms, preferably about 16 to 22 carbon atoms per molecule, and
  • fatty acids include such fatty acids as myristic acid, palmitic acid,
  • stearic acid the various hydroxy s'tearic acids, oleic acid, arachidic acid, behenic acid and the like.
  • -Mixtures in any proportions of these high molecular weight fatty acids are also operable.
  • Naturally occurring high molecular weight acids such as fish oil acids, tallow acids, castor oil acids, coconut oil acids may also be utilized either in their natural state or after partial or complete saturation by hydrogenation.
  • Preferred acids are mixtures derived from natural sources such as hydrogenated fish oil acids,
  • the intermediate molecular Weightacids are those aliphatic monocarboxylic acids containing from about7 to 10 carbon atoms, preferably about 8 to 9 carbon atoms, per molecule. Either saturated or unsaturated fatty acids may be utilized, though the saturated fatty acids are preferred.
  • branched chain acids are useful in the prepara- .tion ofsofter greases, Single or mixed intermediate weight acids having an average saponification valueof 3 from about 310 to 44 0, especially about 320 to 420', are preferred.
  • Suitable acids include:
  • OX0 acids are those formed by the well known Oxo process of synthesis with carbon monoxide, hydrogen and olefins, the latter being 0; and C polymers of propylene with or without some butylene, for making C and C Oxo acids.
  • the medium molecular weight carboxylic acids include straight and branched chain saturated aliphatic carboxylic acids, hydroxy aliphatic monoand poly-carboxylic acids, aromatic monoand poly-carboxylic acids and anhydrides thereof, and heterocyclic acids containing from about 3 to 10, preferably 6 to 9, carbon atoms per molecule.
  • Suitable carboxylic acids are as follows:
  • Pentanoic valeric Glyceric Hexanoic (caproic) Lactic Heptanoic (enanthic) Citric Octanoic (caprylic) Benzoic Nonanoic (pelargonic) Hydroxy benzoic Decanoic (capric) Toluic Isobutyric o-Phthalic C OX0 acids Phthalic anhydride C Oxo acids Terephthalic C Oxo acids Furoic C Oxo acids Thiophene carboxylic Mixed as well as single medium molecular Weight carboxylic acids may be employed in the preparation of these complex thickeners.
  • the low molecular weight carboxylic acids contemplated in this invention include saturated and unsaturated carboxylic acids having from about 1 to 3 carbon atoms, such as formic, acetic, propionic, acyclic and similar acids including their hydroxy derivatives, e.g. lactic acid. Monocarboxylic acids are particularly useful, and acetic acid is especially preferred.
  • the low molecular weight carboxylic acid employed should have a saponification value of above about 600, preferably about 750 to 1300.
  • Mixed low molecular weight carboxylic acids, wherein the acids contain from about 1 to 3 carbon atoms, having saponification values above about 600 may also be employed.
  • the acetic acid can be either glacial acetic acid or an aqueous solution of acetic acid. When the latter is employed, the concentration of acid in solution may vary from about 60 to 99.9 wt. percent, and is preferably about 80 wt. percent.
  • the metal component of the complexes described above is used in a form which can combine chemically with carboxylic acids to form salts or soaps. Ordinarily the metal hydroxide is used.
  • the alkaline earth metal hydroxides or carbonates such as those of calcium, barium and strontium are particularly useful for the purposes of this invention. Calcium hydroxide is especially preferred.
  • the alkaline earth metals differ in this respect from the alkali metals, i.e. sodium, potassium and lithium.
  • Complexes having a high alkali metal content and which consist of the combinations of acids, mol ratios, etc. of the alkaline earth metal complexes of this invention yield greases with poor structural stability. 7 It is preferred, therefore, to use metals having a valency of two. Metals such as magnesium and zinc are also useful for the purposes of this invention.
  • the soap-salt complex thickening agents may be utilized in combination with a Wide variety of mineral as well as synthetic lubricating oils.
  • Mineral base lubricating oils ranging in viscosity from about 30 to 1000 SUS at 100 F. are preferably employed as the liquid phase of the grease composition within the range of about 50 to wt. percent based on the total weight of the final grease composition.
  • These naturally occurring mineral lubricating oils may be derived from any petroleum crude source, whether paraffinic or naphthenic in type, and may be refined by any of the well known refining techniques of the petroleum industry.
  • Suitable synthetic lubricating oils include the hydrocarbon, hydrocarbon polymer, ester, complex ester, formal, mercaptal, polyalkylene oxide, silicone and similar types. Synthetic oils such as di-Z-ethylhexyl sebacate, di-C Oxo azelate and other branched chain simple esters of dicarboxylic acids can be used, as well as complex esters prepared from glycols, dicarboxylic acids, and alcohols or monocarboxylic acids.
  • the high metal content soap-salt complex or salt complexes may be prepared by coneutralization of a mixture of the acids employed with suitable bases, particularly the hydroxides and/or carbonates of the metals desired.
  • This coneutralization step may be carried out in situ in the liquid menstruum to which the complex is to be applied in actual use.
  • the mixed acids may be coneutralized in a portion or all of the lubricating oil forming the dispersant of a grease to be thickened by the soap-salt or salt complexes.
  • the coneutralized material is heated to high temperatures of about 400 to 550 F. or higher prior to use in order to dehydrate the product and to promote the formation of the complex.
  • this heating step is carried out in a liquid dispersant, the latter should have a boiling point above the heating temperature or the heating should be carried out under pressure.
  • the high meta'l soap-salt or salt complexes may also be prepared by separately preforming at least a portion of the high molecular weight carboxylic acid soap, when employed, and/or the low and intermediate molecular weight carboxylic acid salts. This method is particularly useful when different metals are employed as bases.
  • Soap-salt or salt complex proportions of about 530- wt. percent, preferably about 10-20 wt. percent, based on the total grease composition may be employed in preparing the greases constituting component 1 of this invention.
  • Component 2 is a lithium base grease, i.e. a lubricating oil thickened to grease consistency with lithium soaps of high molecular weight carboxylic acids. Mixtures of lithium and strontium or lithium and calcium soaps may also be employed to prepare these greases.
  • the grease-forming fats or high molecular weight fatty acids listed above are also suitable for preparing the component 2 grease.
  • the grease can be made ximm J genesis
  • the conventional methods of grease manufacture such as cooking in a fire heated kettle followed by drawing into thin pans or deep. cakes for cooling may be em ployed in preparing the lithium soap thickened greases. They may also be prepared in steam heated kettles followed by cooling with stirring while running cold water through the kettle jacket or by a continuous method of manufacture.
  • US. Patent 2,397,956 discloses the preparation of greases containing a lithium soap of 12-hydroxy stearic or the lithium soap of hydrogenated castor oil as a thickener.
  • the lithium soaps are present in amounts up to 50%, preferably 8 to 40%, of the total weight of the grease.
  • these greases are preferably prepared at temperatures of between about 400 to 425 F.
  • any suitable lithium compound may be used such as lithium hydroxide, lithium carbonate, lithium oxide and the like.
  • the lithium compound used is lithium monohydrate which contains from 53 to 55% .of lithium hydroxide.
  • operable proportions include from about 20 to 80% of component 1 and from about 20 to 80% of component 2.
  • Preferred proportions are from about 40 to 80% of component 1 and from about 20 to 60% of component 2.
  • the temperatures of blending are within the range of about 100 to 300 F., preferably about 180 to 225 F.
  • the maximum temperature range may be just below the phase change in the lithium grease, i.e. when the grease changes in structure from a rubbery fibrous product to a smooth homogeneous product.
  • the two grease components are blended together by thorough mixing or by being passed through a Gaulin homogenizer or Morehouse mill at a temperature suflicient to give an outlet temperature below the phase change of the lithium soap thickened grease component.
  • Grease B I A grease was prepared from the following ingredients:
  • the fatty acid and about one half of the mineral oil were added to steam kettle, and the calcium hydroxide was stirred in at a temperature of about 155 F. Heating and stirring were continued, and the lithium hydroxide added as a 10% aqueous solution at a temperature of 198 F.
  • the grease batch was then heated to a temperature of about 290 F. to eifect dehydration. During this period the viscosity of the mass was cut down by the addition of small amounts of oil. Thereafter the heat was shut oif, and the balance of the mineral oil added while stirring over a period of about 1 to 2 hours.
  • the grease was finished by being passed through a Morehouse rnillat an inlet temperature of about 90 F. and an outlet temperature of about 118 F.
  • Greases C, D, E and F These greases were prepared by blending Greases A and B, separately prepared as described above, in accordance with formulations listed in the table below at a temperature of 125 F.
  • Grease G A grease was prepared from the following ingredients:
  • the mixture 'of acetic acid and caprylic acid was charged to the kettle, and the temperature raised with stirring to about 480 F. At this temperature, heating was discontinued and the mixture cooled to about 250 F. with stirring. Phenyl alpha naphthylamine was. then added, and cooling continued to a temperature of about 200 F. The resulting grease composition was milled through a Gaulin homogenizer and filtered.
  • Grease H A grease was prepared from the following ingredients:
  • the methyl 12-hydroxy stearate and the mineral oil were charged to a fire heated kettle and warmed while mixing to F.
  • a 20% aqueous boiling water solution of the lithium monohydrate was then added and the grease heated to 400 F.
  • the fluid grease was cooled while stirring to 350 F. where the grease was just starting to solidify.
  • the phenyl alpha naphthylamine was then added, and the grease drawn into pans for cooling.
  • Greases I, J, K, L and M These greases were prepared by blending Greases G and H, separately prepared as described above, in accordance with the formulations listed in the table below at a temperature of 180 F.
  • this invention relates to new and improved lubricating grease compositions comprising blends of l) soap-salt complex or mixed salt complex thickened greases having a high combined metal content and (2) lithium soap thickened greases.
  • the blended grease compositions prepared in accordance with the invention have lubricating lives superior to the individual lithium soap thickened greases and a water resistance superior to the individual complex thickened greases.
  • Blends containing from about 20' The invention is not necessarily limited to the specific conditions and materials of the foregoing example. These conditions and materials may be varied within the limits indicated in the general portions of the specification. Moreover, the conventional grease additives such as oxidation inhibitors, pour point depressors, corrosion inhibitors and the like can be effectively incorporated in the grease blends of this invention.
  • a blended grease composition comprising a blend of two component greases, one component being a grease thickened with a calcium mixed salt complex of lowand intermediate molecular weight mono-carboxylic acids, wherein the mol ratio of low to intermediate weight acid is about 2:1 to 40:1, the other component being a lithium base grease thickened with the lithium soap of a highmolecular weight fatty acid, said blend consisting essentially of from 40 to 80% by Weight of the first component and 20 to by weight of the second component.
  • blended grease composition of claim 1 wherein said blend consists essentially of from about 40 to 60% by weight of the first component and from about 40 to 60% by weight of'the second component.
  • the blended grease composition of claim 1, wherein said calcium mixed salt complex is a mixed salt complex of a low molecular weight carboxylicacid having from 1 to 3 carbon atoms per molecule and an intermediate molecular weight carboxylic acid having from 7 to 10 carbon atoms per molecule.
  • the blended grease composition of claim 1 wherein the first component is a grease thickened with the mixed salt complex of calcium acetate and calcium caprylate, and the second component is a lithium base grease thickened with lithium 12-hydroxystearate said blend consisting essentially of from about 40 to 60% by weight of the first component and 40 to 60% by weight of the second component.

Description

United States Patent O "ice BLENDED LITHIUM CALCIUM BASE GREASE Arnold J. Morway, Clark, N.J., assignor to Esso Research and Engineering Company, a corporation of Delaware No Drawing. Application April 28, 1955 Serial No. 504,659
'5 Claims. (Cl. 252-40) This invention relates to improved lubricating grease compositions having outstanding lubricating life and water resistance characteristics. More particularly, the invention "pertains to blends of separate grease components to form' greases having excellent water emulsion stability and long lubrication service.
In brief compass, the invention relates to lubricating grease compositions comprising a blend of two component greases, one component being a lubricating oil thickened to grease consistency with an organo-metallic soap-salt or mixed salt complex, having a high combined but active metal content, and the other component being a lithium soap thickened grease. These two-component greases areimade separately and then blended togetherby thorough mixing or by the use of a suitable homogenizer or grease mill.
The use of organo-metallic complexes having high metal content as grease thickeners has recently been suggested. In general, these complex thickeners have been prepared from the metal salts of low molecular weight carboxylic acids in combination with metal soaps ofhigh molecular weight carboxylic acids, metal salts of intermediate molecular weight carboxylic acids, or metal salts of medium molecular weight carboxylioacids 'and metal soaps of high molecular weight ca'rboxylicacids. The metal constituents of the complex thickeners have usually been selected from the 'divalent metals, especially the alkaline earth metals. Calcium is particularly preferred. Greases containing these complex thickeners have been found to have outstanding extreme pressure properties and long lubricating lives, but they tend to form fluid emulsions when water is churned into them. f
;The use of lithium soaps in grease-making is well known in theart. Such lithium soap type thickeners have been prepared from the conventional soap-forming high molecular weight carboxylic acids, including their hydroxy derivatives and esters thereof. Lithium-containing grease thickeners have also been prepared from mixtures of lithium and calcium soaps of high; molecular Weight fatty acids. Greases thickened with these lithiumcontaining soaps, such asthe lithium soap of hydroxy stearic acid, haveexcellent water resistance but notably poor lubricating lives.
In US. Patent No. 2,397,956 Fraser teaches the preparation :of alubricating grease using a lithium soap of 12-hydroxy stearic acid or hydrogenated castor oil. patent also discloses that the calcium soap of a high molecular weight fatty acid, preferably as a preformed The content organo-metallic complex thickened greases and the lithium soap thickened greases may be prepared by v blending from about 20 to 60% of the lithium base grease an organo-metalliccomplex thickener, having a high combined but active metal content. eners include the following:
(a) The soap-salt complexes prepared from the met-a1 salts of low molecular weight carboxylic acids having Suitable complex thickfrom 1 to 3 carbon atoms per molecule, and the metal soaps of high molecular weight carboxylic acids'having from 12 to 30 carbon atoms per molecule, whereinthe mol ratio of the low to high molecular weight acids is about 7:1 to 40:1, preferably about 8:1 to 25:1;
(b) The mixed salt complexes prepared from the metal salts of low molecular weight carboxylic acids having from 1 to 3 carbon atoms per molecule, and metal salts of intermediate molecular weight carboxylic acids having from 7 to 10 carbon atoms per molecule, wherein the mol ratio of low to intermediate weight acids is about 2:1 to 40:1, preferably about 4:1 to 25:1;
(c) The soap-salt complexes prepared from the met-a1 salt of acetic acid, metal salts of medium molecular Weight carboxylic acids having from 3 to 10 carbon atoms per molecule, and metal soaps of high molecular weight carboxylic acids having from 12 to 30 carbon atoms per molecule; wherein the mol ratio of acetic to the medium and high molecular weight acid is about 4:1 to 40:1, the mol ratio ofmedium to high molecular weight acids is about'0.5:1 to 10:1, and the difference in number; of
carbon atoms per molecule between the high and medium molecular weight carboxylic acid is at least 7, preferably about 7 to 15.
The high molecular Weight carboxylic acids useful for preparing the complex thickeners described above are those saturated and unsaturated, grease-making fatty acids thatare commonly known to the art. In general, these fatty acids have from about 12 to 30 carbon atoms, preferably about 16 to 22 carbon atoms per molecule, and
include such fatty acids as myristic acid, palmitic acid,
stearic acid, the various hydroxy s'tearic acids, oleic acid, arachidic acid, behenic acid and the like. -Mixtures in any proportions of these high molecular weight fatty acids are also operable. Naturally occurring high molecular weight acids such as fish oil acids, tallow acids, castor oil acids, coconut oil acids may also be utilized either in their natural state or after partial or complete saturation by hydrogenation. Preferred acids are mixtures derived from natural sources such as hydrogenated fish oil acids,
i animal fatty acids and the like.
co'rporating the desirable characteristics ofthe high metal The intermediate molecular Weightacids are those aliphatic monocarboxylic acids containing from about7 to 10 carbon atoms, preferably about 8 to 9 carbon atoms, per molecule. Either saturated or unsaturated fatty acids may be utilized, though the saturated fatty acids are preferred.
Straight chain or substantially straight chain acids are preferred in the preparation of relatively firm greases;
While the branched chain acids are useful in the prepara- .tion ofsofter greases, Single or mixed intermediate weight acids having an average saponification valueof 3 from about 310 to 44 0, especially about 320 to 420', are preferred. Suitable acids include:
S-methyl-Z-hexanoic Heptanoic (enanthic) Octanoic (caprylic) 2-ethyl hexanoic C OX acid Nonanoic (pelargonic) Decanoic (capric) C OXo acids The OX0 acids are those formed by the well known Oxo process of synthesis with carbon monoxide, hydrogen and olefins, the latter being 0; and C polymers of propylene with or without some butylene, for making C and C Oxo acids.
The medium molecular weight carboxylic acids, as designated for the purposes of this invention, include straight and branched chain saturated aliphatic carboxylic acids, hydroxy aliphatic monoand poly-carboxylic acids, aromatic monoand poly-carboxylic acids and anhydrides thereof, and heterocyclic acids containing from about 3 to 10, preferably 6 to 9, carbon atoms per molecule. Suitable carboxylic acids are as follows:
Pentanoic (valeric) Glyceric Hexanoic (caproic) Lactic Heptanoic (enanthic) Citric Octanoic (caprylic) Benzoic Nonanoic (pelargonic) Hydroxy benzoic Decanoic (capric) Toluic Isobutyric o-Phthalic C OX0 acids Phthalic anhydride C Oxo acids Terephthalic C Oxo acids Furoic C Oxo acids Thiophene carboxylic Mixed as well as single medium molecular Weight carboxylic acids may be employed in the preparation of these complex thickeners.
The low molecular weight carboxylic acids contemplated in this invention include saturated and unsaturated carboxylic acids having from about 1 to 3 carbon atoms, such as formic, acetic, propionic, acyclic and similar acids including their hydroxy derivatives, e.g. lactic acid. Monocarboxylic acids are particularly useful, and acetic acid is especially preferred. In general, the low molecular weight carboxylic acid employed should have a saponification value of above about 600, preferably about 750 to 1300. Mixed low molecular weight carboxylic acids, wherein the acids contain from about 1 to 3 carbon atoms, having saponification values above about 600 may also be employed. The acetic acid can be either glacial acetic acid or an aqueous solution of acetic acid. When the latter is employed, the concentration of acid in solution may vary from about 60 to 99.9 wt. percent, and is preferably about 80 wt. percent.
The metal component of the complexes described above is used in a form which can combine chemically with carboxylic acids to form salts or soaps. Ordinarily the metal hydroxide is used. The alkaline earth metal hydroxides or carbonates such as those of calcium, barium and strontium are particularly useful for the purposes of this invention. Calcium hydroxide is especially preferred. The alkaline earth metals differ in this respect from the alkali metals, i.e. sodium, potassium and lithium. Complexes having a high alkali metal content and which consist of the combinations of acids, mol ratios, etc. of the alkaline earth metal complexes of this invention yield greases with poor structural stability. 7 It is preferred, therefore, to use metals having a valency of two. Metals such as magnesium and zinc are also useful for the purposes of this invention.
The soap-salt complex thickening agents may be utilized in combination with a Wide variety of mineral as well as synthetic lubricating oils. Mineral base lubricating oils ranging in viscosity from about 30 to 1000 SUS at 100 F. are preferably employed as the liquid phase of the grease composition within the range of about 50 to wt. percent based on the total weight of the final grease composition. These naturally occurring mineral lubricating oils may be derived from any petroleum crude source, whether paraffinic or naphthenic in type, and may be refined by any of the well known refining techniques of the petroleum industry.
Suitable synthetic lubricating oils include the hydrocarbon, hydrocarbon polymer, ester, complex ester, formal, mercaptal, polyalkylene oxide, silicone and similar types. Synthetic oils such as di-Z-ethylhexyl sebacate, di-C Oxo azelate and other branched chain simple esters of dicarboxylic acids can be used, as well as complex esters prepared from glycols, dicarboxylic acids, and alcohols or monocarboxylic acids.
The high metal content soap-salt complex or salt complexes may be prepared by coneutralization of a mixture of the acids employed with suitable bases, particularly the hydroxides and/or carbonates of the metals desired. This coneutralization step may be carried out in situ in the liquid menstruum to which the complex is to be applied in actual use. For example, the mixed acids may be coneutralized in a portion or all of the lubricating oil forming the dispersant of a grease to be thickened by the soap-salt or salt complexes. The coneutralized material is heated to high temperatures of about 400 to 550 F. or higher prior to use in order to dehydrate the product and to promote the formation of the complex. When this heating step is carried out in a liquid dispersant, the latter should have a boiling point above the heating temperature or the heating should be carried out under pressure.
The high meta'l soap-salt or salt complexes may also be prepared by separately preforming at least a portion of the high molecular weight carboxylic acid soap, when employed, and/or the low and intermediate molecular weight carboxylic acid salts. This method is particularly useful when different metals are employed as bases.
Soap-salt or salt complex proportions of about 530- wt. percent, preferably about 10-20 wt. percent, based on the total grease composition may be employed in preparing the greases constituting component 1 of this invention.
The constitution and chemical structure of the soapsalt and mixed salt complexes are not fully understood. X-ray difiraction spectra obtained from various soapsalt and salt complexes do show, however, patterns defi-.
nitely inconsistent with those of physical mixtures of the soap and salt or mixtures of salts. Moreover, the spectra show that the temperature to which the complex components are heated or reacted is important. Patterns obtained from heating complex components to a temperature within the range of about 400 to 550 F. and at lower temperatures clearly differ from each other indicating different products. Accordingly, for the purposes of this invention as well as for consistency with terminology already established by the art, the products obtained by heating mixtures of high molecular weight carboxylic acid soap with lower molecular weight carboxylic acid salt; low and intermediate molecular weight carboxylic acid salts; or low and medium molecular weight acid salts with high molecular weight carboxylic acid soaps within the aforementioned, temperature range are designated as complexes. It is almost certain that these complexes are not ordinary chemical compounds, but rather some sort of Werner complex with coordinated valences.
Component 2 is a lithium base grease, i.e. a lubricating oil thickened to grease consistency with lithium soaps of high molecular weight carboxylic acids. Mixtures of lithium and strontium or lithium and calcium soaps may also be employed to prepare these greases.
The grease-forming fats or high molecular weight fatty acids listed above are also suitable for preparing the component 2 grease. Thus, the grease can be made ximm J genesis The conventional methods of grease manufacture such as cooking in a fire heated kettle followed by drawing into thin pans or deep. cakes for cooling may be em ployed in preparing the lithium soap thickened greases. They may also be prepared in steam heated kettles followed by cooling with stirring while running cold water through the kettle jacket or by a continuous method of manufacture.
US. Patent 2,641,577 contains a detailed description of the composition and preparation of a lithium-calcium lubricating grease composition suitable for use as component 2 of this invention. As disclosed in this patent, the mol ratios of the lithium soap to the calciumsoap may vary between about 2:1 to 8:1, the preferred ratio being about 3:1 to 6:1. H
US. Patent 2,397,956 discloses the preparation of greases containing a lithium soap of 12-hydroxy stearic or the lithium soap of hydrogenated castor oil as a thickener. The lithium soaps are present in amounts up to 50%, preferably 8 to 40%, of the total weight of the grease. In addition, these greases are preferably prepared at temperatures of between about 400 to 425 F.
In preparing greases containing a lithium soap any suitable lithium compound may be used such as lithium hydroxide, lithium carbonate, lithium oxide and the like. Preferably, however, the lithium compound used is lithium monohydrate which contains from 53 to 55% .of lithium hydroxide.
In blending the grease components of this invention, operable proportions include from about 20 to 80% of component 1 and from about 20 to 80% of component 2. Preferred proportions, however, are from about 40 to 80% of component 1 and from about 20 to 60% of component 2. The temperatures of blending are within the range of about 100 to 300 F., preferably about 180 to 225 F. The maximum temperature range may be just below the phase change in the lithium grease, i.e. when the grease changes in structure from a rubbery fibrous product to a smooth homogeneous product. As described above, the two grease components are blended together by thorough mixing or by being passed through a Gaulin homogenizer or Morehouse mill at a temperature suflicient to give an outlet temperature below the phase change of the lithium soap thickened grease component.
The invention will be more fully understood by reference to the following example illustrating various modifications of the invention.
EXAMPLE Grease A A grease was prepared from the following ingredients:
7.2% glacial acetic acid 1.8% Hydrofol Acid 51 1.8% hydrogenated castor oil 5.4% hydrated lime 0.4% phenyl alpha naphthylamine 83.4% mineral lubricating oil, 55 SUS/210 F.
added. Heating was continued and the temperature was raised to 500 F., at which time heating was discon-' tinned and the grease was cooled to 200 F. while stirring. Thereafter, the grease was homogenized in a Gaulin homogenizer. The ratio of the acetic to the higher acids was about 10:1. 1
Grease B I A grease was prepared from the following ingredients:
8.41% animal fatty acid 0.48% hydrated lime 1.01% lithium monohydrate 90.11% mineral lubricating oil, 70 SUS/ 210 F.
The fatty acid and about one half of the mineral oil were added to steam kettle, and the calcium hydroxide was stirred in at a temperature of about 155 F. Heating and stirring were continued, and the lithium hydroxide added as a 10% aqueous solution at a temperature of 198 F. The grease batch was then heated to a temperature of about 290 F. to eifect dehydration. During this period the viscosity of the mass was cut down by the addition of small amounts of oil. Thereafter the heat was shut oif, and the balance of the mineral oil added while stirring over a period of about 1 to 2 hours. The grease was finished by being passed through a Morehouse rnillat an inlet temperature of about 90 F. and an outlet temperature of about 118 F.
Greases C, D, E and F These greases were prepared by blending Greases A and B, separately prepared as described above, in accordance with formulations listed in the table below at a temperature of 125 F.
Grease G A grease was prepared from the following ingredients:
15.0% glacial acetic acid 3.6% caprylic acid 11.1% hydrated lime 0.5% phenyl alpha naphthylamine 69.8% mineral lubricating oil, 55 SUS/210 F.
The hydrated lime and all of the mineral lubricating The temperature of the kettle was then raised to about F. with stirring. When this temperature was reached,
the mixture 'of acetic acid and caprylic acid was charged to the kettle, and the temperature raised with stirring to about 480 F. At this temperature, heating was discontinued and the mixture cooled to about 250 F. with stirring. Phenyl alpha naphthylamine was. then added, and cooling continued to a temperature of about 200 F. The resulting grease composition was milled through a Gaulin homogenizer and filtered.
Grease H A grease was prepared from the following ingredients:
12.00% methyl 12-hydroxy stearate 1.68% lithium monohydrate 0.50% phenyl alpha naphthylamine 85.82% mineral lubricating oil, 55 SUS/2l0 F.
The methyl 12-hydroxy stearate and the mineral oil were charged to a fire heated kettle and warmed while mixing to F. A 20% aqueous boiling water solution of the lithium monohydrate was then added and the grease heated to 400 F. The fluid grease was cooled while stirring to 350 F. where the grease was just starting to solidify. The phenyl alpha naphthylamine was then added, and the grease drawn into pans for cooling.
Greases I, J, K, L and M These greases were prepared by blending Greases G and H, separately prepared as described above, in accordance with the formulations listed in the table below at a temperature of 180 F.
1 Stoppeddidnt fail.
It will be noted that the water resistance ability of calcium complex thickened greases and the lubricating life of lithium soap thickened greases can be improved by blending the separately prepared greases in certain definite proportions. to 60% of a lithium soap thickened grease impart good water emulsion stability to the calcium complex thickened grease. See Greases C, D, E, I, J, K, L and M. By employing a grease thickened with a lithium soap the methyl ester of 12-hydroxy stearic acid in conjunction with a calcium caprylate-acetate complex thickened grease, the lubricating life of the final grease composition was markedly increased while satisfactory water resistance was maintained. See Grease J.
In summation, this invention relates to new and improved lubricating grease compositions comprising blends of l) soap-salt complex or mixed salt complex thickened greases having a high combined metal content and (2) lithium soap thickened greases. The blended grease compositions prepared in accordance with the invention have lubricating lives superior to the individual lithium soap thickened greases and a water resistance superior to the individual complex thickened greases.
Blends containing from about 20' The invention is not necessarily limited to the specific conditions and materials of the foregoing example. These conditions and materials may be varied within the limits indicated in the general portions of the specification. Moreover, the conventional grease additives such as oxidation inhibitors, pour point depressors, corrosion inhibitors and the like can be effectively incorporated in the grease blends of this invention.
What is claimed is:
1. A blended grease composition comprising a blend of two component greases, one component being a grease thickened with a calcium mixed salt complex of lowand intermediate molecular weight mono-carboxylic acids, wherein the mol ratio of low to intermediate weight acid is about 2:1 to 40:1, the other component being a lithium base grease thickened with the lithium soap of a highmolecular weight fatty acid, said blend consisting essentially of from 40 to 80% by Weight of the first component and 20 to by weight of the second component.
2. The blended grease composition of claim 1, Wherein said blend consists essentially of from about 40 to 60% by weight of the first component and from about 40 to 60% by weight of'the second component.
3'. The blended grease composition of claim 1, wherein said calcium mixed salt complex .is a mixed salt complex of a low molecular weight carboxylicacid having from 1 to 3 carbon atoms per molecule and an intermediate molecular weight carboxylic acid having from 7 to 10 carbon atoms per molecule.
4. The blended grease composition of claim 1, where in said lithium base grease is thickened with lithium 12- hydroxystearate.
' 5. The blended grease composition of claim 1, wherein the first component is a grease thickened with the mixed salt complex of calcium acetate and calcium caprylate, and the second component is a lithium base grease thickened with lithium 12-hydroxystearate said blend consisting essentially of from about 40 to 60% by weight of the first component and 40 to 60% by weight of the second component.
References Cited in the file of this patent UNITED STATES PATENTS 2,397,956 Fraser Apr. 9, 1946 2,417,428 McLennan Mar. 18, 1947 2,641,577 OHalloran June 9', 1953 2,844,536 Morway July 22, 1958

Claims (1)

1. A BLENDED GREASE COMPOSITION COMPRISING A BLEND OF TWO COMPONENT GREASES, ONE COMPONENT BEING A GREASE THICKENED WITH A CALCIUM MIXED SALT COMPLEX OF LOW AND INTERMEDIATE MOLECULAR WEIGHT MONO-CARBOXYLIC ACIDS, WHEREIN THE MOL RATIO OF LOW TO INTERMEDIATE WEIGHT ACID IS ABOUT 2:1 TO 40:1, THE OTHER COMPONENT BEING A LITHIUM BASE GREASE THICKENED WITH THE LITHIUM SOAP OF A HIGH MOLECULAR WEIGHT FATTY ACID, SAID BLEND CONSISTING ESSENTIALLY OF FROM 40 TO 80% BY WEIGHT OF THE FIRST COMPONENT AND 20 TO 60% BY WEIGHT OF THE SECOND COMPONENT.
US504659A 1955-04-28 1955-04-28 Blended lithium calcium base grease Expired - Lifetime US2908645A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
NL104990D NL104990C (en) 1955-04-28
BE546805D BE546805A (en) 1955-04-28
US504659A US2908645A (en) 1955-04-28 1955-04-28 Blended lithium calcium base grease
GB9885/56A GB793484A (en) 1955-04-28 1956-03-29 Improved grease compositions
FR1152678D FR1152678A (en) 1955-04-28 1956-04-18 Compound lubricating greases
DEE12287A DE1064667B (en) 1955-04-28 1956-04-24 Grease and process for its manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US504659A US2908645A (en) 1955-04-28 1955-04-28 Blended lithium calcium base grease

Publications (1)

Publication Number Publication Date
US2908645A true US2908645A (en) 1959-10-13

Family

ID=24007212

Family Applications (1)

Application Number Title Priority Date Filing Date
US504659A Expired - Lifetime US2908645A (en) 1955-04-28 1955-04-28 Blended lithium calcium base grease

Country Status (6)

Country Link
US (1) US2908645A (en)
BE (1) BE546805A (en)
DE (1) DE1064667B (en)
FR (1) FR1152678A (en)
GB (1) GB793484A (en)
NL (1) NL104990C (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3223633A (en) * 1963-07-01 1965-12-14 Exxon Research Engineering Co Lubricant
US3298953A (en) * 1964-04-01 1967-01-17 Exxon Research Engineering Co Lubricants containing mixed metal salts of fatty acid and aromatic polybasic acid
US3389085A (en) * 1964-03-31 1968-06-18 Exxon Research Engineering Co Lubricants containing mixed metal salts of mono- and polybasic acids
US5015403A (en) * 1990-03-23 1991-05-14 Shell Oil Company Preparation of lithium-calcium grease compositions
WO2015021052A1 (en) * 2013-08-05 2015-02-12 Sr Lubricant Solutions, Llc Lubricant with spherical copper and bismuth powders

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL258842A (en) * 1959-12-11
DE2027403C2 (en) * 1970-06-04 1983-12-15 Exxon Research and Engineering Co., 07036 Linden, N.J. Permanent grease

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2397956A (en) * 1943-01-15 1946-04-09 Internat Lubricant Corp Production of lubricants
US2417428A (en) * 1946-09-19 1947-03-18 Union Oil Co Lubricating composition
US2641577A (en) * 1951-06-22 1953-06-09 Standard Oil Dev Co Lithium-calcium lubricating grease composition
US2844536A (en) * 1954-04-30 1958-07-22 Exxon Research Engineering Co High temperature complex grease manufacturing processes

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2712527A (en) * 1952-08-26 1955-07-05 Exxon Research Engineering Co Improved lubricating greases containing dihydroxy stearic acid soap

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2397956A (en) * 1943-01-15 1946-04-09 Internat Lubricant Corp Production of lubricants
US2417428A (en) * 1946-09-19 1947-03-18 Union Oil Co Lubricating composition
US2641577A (en) * 1951-06-22 1953-06-09 Standard Oil Dev Co Lithium-calcium lubricating grease composition
US2844536A (en) * 1954-04-30 1958-07-22 Exxon Research Engineering Co High temperature complex grease manufacturing processes

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3223633A (en) * 1963-07-01 1965-12-14 Exxon Research Engineering Co Lubricant
US3389085A (en) * 1964-03-31 1968-06-18 Exxon Research Engineering Co Lubricants containing mixed metal salts of mono- and polybasic acids
US3298953A (en) * 1964-04-01 1967-01-17 Exxon Research Engineering Co Lubricants containing mixed metal salts of fatty acid and aromatic polybasic acid
US5015403A (en) * 1990-03-23 1991-05-14 Shell Oil Company Preparation of lithium-calcium grease compositions
WO2015021052A1 (en) * 2013-08-05 2015-02-12 Sr Lubricant Solutions, Llc Lubricant with spherical copper and bismuth powders

Also Published As

Publication number Publication date
BE546805A (en)
FR1152678A (en) 1958-02-21
NL104990C (en)
DE1064667B (en) 1959-09-03
GB793484A (en) 1958-04-16

Similar Documents

Publication Publication Date Title
US3929651A (en) Modified lithium soap grease
US2976242A (en) Lubricating grease compositions
US2607735A (en) Alkaline earth metal soap greases
US2468098A (en) Grease composition
US2528373A (en) Alkenyl succinic acid grease
US2908645A (en) Blended lithium calcium base grease
US2863847A (en) Lubricating oils thickened to a grease with hydrous metal salts and process for forming same
US3068175A (en) Process for preparing complex calcium salt-calcium soap grease
GB601346A (en) Improvements in or relating to lithium base lubricating grease compositions and method of preparing the same
US2641577A (en) Lithium-calcium lubricating grease composition
US2985590A (en) Lubricating oil compositions comprising mercaptobenzothiazole ester derivatives
US2833718A (en) Lubricating composition containing polyethylene resins
US3985662A (en) High dropping point greases comprising a lithium soap of an epoxy-substituted and/or an ethylenically unsaturated fatty acid
US2856362A (en) Lubricating compositions
US3068174A (en) Process for preparing complex calcium salt-calcium soap grease
US2870090A (en) Method of grease manufacture comprising shearing
US2503749A (en) Barium soap grease compositions and method of preparation
US2844536A (en) High temperature complex grease manufacturing processes
US2755247A (en) Wide temperature range alkali metal grease containing excess alkali metal hydroxides
US2610947A (en) Lubricating grease and process of manufacture
US2880174A (en) Soap-salt complex thickened greases
US2589973A (en) Lubricating grease composition
US3389085A (en) Lubricants containing mixed metal salts of mono- and polybasic acids
US2888402A (en) Process for preparing lubricating greases
US2929781A (en) Process for making a lithium-calcium base grease