US3798164A - Polyoxyalkylene bis-thiourea extreme pressure agents and methods of use - Google Patents

Polyoxyalkylene bis-thiourea extreme pressure agents and methods of use Download PDF

Info

Publication number
US3798164A
US3798164A US00289203A US3798164DA US3798164A US 3798164 A US3798164 A US 3798164A US 00289203 A US00289203 A US 00289203A US 3798164D A US3798164D A US 3798164DA US 3798164 A US3798164 A US 3798164A
Authority
US
United States
Prior art keywords
extreme pressure
agents
thioureas
methyl
thiourea
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
US00289203A
Inventor
T Kmet
J Loboda
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.)
Richardson Co
Original Assignee
Richardson 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
Application filed by Richardson Co filed Critical Richardson Co
Application granted granted Critical
Publication of US3798164A publication Critical patent/US3798164A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C335/00Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C335/04Derivatives of thiourea
    • C07C335/06Derivatives of thiourea having nitrogen atoms of thiourea groups bound to acyclic carbon atoms
    • C07C335/08Derivatives of thiourea having nitrogen atoms of thiourea groups bound to acyclic carbon atoms of a saturated carbon skeleton
    • 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
    • C10M173/00Lubricating compositions containing more than 10% water
    • C10M173/02Lubricating compositions containing more than 10% water not containing mineral or fatty 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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
    • 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
    • C10M2205/18Natural waxes, e.g. ceresin, ozocerite, bees wax, carnauba; Degras
    • 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
    • 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/027Neutral 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
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/046Hydroxy ethers
    • 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
    • C10M2207/18Tall oil 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
    • C10M2207/20Rosin 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
    • C10M2207/281Esters 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
    • C10M2207/284Esters of aromatic 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
    • C10M2207/285Esters of aromatic polycarboxylic 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
    • C10M2207/286Esters 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
    • 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
    • C10M2209/104Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
    • 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
    • C10M2209/107Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106
    • 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
    • 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
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/221Six-membered rings containing nitrogen and carbon only
    • 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
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • 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
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • C10M2215/226Morpholines
    • 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
    • C10M2215/30Heterocyclic 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/042Sulfate 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • 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
    • C10M2219/06Thio-acids; Thiocyanates; Derivatives thereof
    • C10M2219/062Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
    • C10M2219/064Thiourea type 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
    • C10M2221/00Organic macromolecular compounds containing sulfur, selenium or tellurium 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
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/041Triaryl phosphates
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/22Metal working with essential removal of material, e.g. cutting, grinding or drilling
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/24Metal working without essential removal of material, e.g. forming, gorging, drawing, pressing, stamping, rolling or extruding; Punching metal
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/241Manufacturing joint-less pipes
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/242Hot working
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/243Cold working
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/245Soft metals, e.g. aluminum
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/246Iron or steel
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/247Stainless steel
    • 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
    • C10N2050/01Emulsions, colloids, or micelles

Definitions

  • x and y are numbers from 1 to 20.
  • R represents 30 carbon atoms and n is 1 to 20.
  • This group includes ethoxylated cetyl, stearyl or oleyl alcohols having moles of ethylene oxide.
  • Others are the polyoxyethylene substituted N,N' fatty acid amides available under the trademark Ethomid by Armour.
  • EP lubricants of the present invention are used in an amount sufficient to provide anti-weld properties. Though not required in each instance, it is advantageous to employ in complete compositions the aforementioned boundary lubricants in an amount suflicient to enhance or activate the performance of the EP agent.
  • the ratio of EP agent to boundary lubricant is used in the range from about 1:1 to 1:30.
  • the combined concentration of EP agent and boundary lubricant in formulations should be from 2% to 85%, and when diluted for use, should have a concentration ranging from about 0.03% to 5% and preferably about 0.1% to 3.0%.
  • the above product was prepared according to the method of Example I, however, the polyether diamine starting material had a molecular weight of 230 and x was 2.6.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Lubricants (AREA)

Abstract

NOVEL SUBSTITUTED AND UNSUBSTITUTED POLYOXYALKYLENE BIS-THIOUREAS HAVING THE FORMULA: R-NH-C(=S)-NH-CH(-Y)-CH2-(O-CH2-CH(-Y))X-NH-C(=S)-NH-R WHEREIN X IS A NUMBER FROM 1 TO 10, R AND R1 ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, ALKYL AND ALKENYL, Y IS HYDROGEN OR LOWER ALKYL, ARE USEFUL AS EXTREME PRESSURE LUBRICANTS IN METAL WORKING FLUIDS AND PARTICULARLY IN AQUEOUS TYPE FLUIDS. COMPOSITIONS COMPRISING THE THIOUREAS AND A BOUNDARY LUBRICANT PROVIDE THE ANTI-WELD AND FRICTION REDUCTION PROPERTIES NECESSARY FOR HEAVY DUTY MACHINING.

Description

United States Patent ()1 ice 3,798,164 Patented Mar. 19, 1974 POLYOXYALKYLENE BIS-THIOUREA EXTREME PRESSURE AGENTS AND METHODS OF USE Thomas J. Kmet, Midlothian, and Jon A. Loboda, Chicago, Ill., assignors to The Richardson Company, Melrose Park, 1]].
No Drawing. Original application May 24, 1971, Ser. No. 146,535, now Patent No. 3,704,321. Divided and this application Sept. 14, 1972, Ser. No. 289,203
Int. Cl. Cm 1/06, 1/38 U.S. Cl. 252-475 6 Claims ABSTRACT OF THE DISCLOSURE Novel substituted and unsubstituted polyoxyalkylene bis-thioureas having the formula:
BACKGROUND OF THE INVENTION This invention relates to a series of new and useful bisthiourea compounds including compositions and methods of using the same in machining operations. More specifically, it has been discovered that certain novel polyoxyalkylene bis-thioureas and their compositions perform as extreme pressure agents when incorporated into metal working fluids. The invention is founded on the realization that superior extreme pressure lubrication can be expected in heavy duty machining operations particularly with aqueous base cutting fluids when used in conjunction with the thioureas defined herein below. The instant thioureas are significant in that there are few sulfur containing extreme pressure agents available which can be effectively employed in a wide range of aqueous systems. Thus, the instant compounds permit water based metal working solutions and emulsions to be used in a broader range of machining applications including heavy duty grinding and cutting operations.
Briefly, it has been discovered that a series of thioureas having the formula:
wherein x is a number from 1 to 10 and R and R are selected from the group consisting of hydrogen, alkyl and alkenyl and Y is hydrogen or lower alkyl, perform as extreme pressure (EP) agents in metal working fluids and particularly those containing water.
Along with the extreme pressure agents shown herein, it is often desirable though not required in each instance to also employ boundary lubricants. Boundary lubrication is ordinarily used in machining operations to prevent heat build-up and unwanted wear which liquids such as water, hydrocarbon oils, silicones etc. are unable to control especially as conditions become more extreme. However, it has been found that polar type boundary lubricants perform particularly well with the above mentioned thioureas. It is believed that these lubricants act with the extreme pressure agents to more effectively release sulfur from the thioureas to form protective iron sulfide films on the surface of the workpiece when subjected to conditions of high pressure and temperature. Therefore, in addition to novel polyoxyalkylene bis thioureas, the present invention also contemplates compositions of said thioureas advantageously used with boundary lubricants sometimes referred to as lubricity agents to enhance the activity of the extreme pressure component.
As previously indicated, the EP additives of the present invention provide the necessary friction modification and wear reduction as well as galling and seizing reducing properties making them highy versatile and satisfactory extreme pressure lubricants, especially useful in aqueous metal working fluids. Heretofore, compositions used in heavy-duty machining operations were mostly limited to non-aqueous or oil-based fluids. Aqueous metal working fluids, on the other hand, ordinarily in the form of solution or emulsion comprised of water or diluted with water prior to use and perhaps containing in addition a boundary lubricant additive such as fatty acid soaps including sulfoesters, alkyl taurines, alkylpolyamines, polyethylene glycols, petroleum sulfonate, sulfoaminoacetates, have been limited to machining operations where only relatively light or mild pressure between the work and cutting tool would be employed.
Generally, Water based metal working fluids used under light pressure provide suflicient lubrication to prevent metal-to-metal contact. However, as pressures and temperatures rise between work and tool to more extreme conditions, water-based compositions are unable to supply sufficient friction reduction or boundary lubrication. Frequently, pressure between the sliding chip and tool face is in the order of 100,000 p.s.i. with temperatures in the area of contact at 1000 F. or more. Under these conditions, aqueous films with boundary lubricants commonly break down, greatly diminishing tool life and quality of finish on the work.
Sulfur containing metal working lubricants and extreme pressure agents such as sulfurized mineral and fatty oils, sulfochlorinated oils and the like, have been used with some success. However, such products have not been entirely satisfactory in many instances. Frequently, extreme pressure soluble oils made with conventional sulfurized fatty additives have been undependable because of their instability. Blends of conventional sulfur containing extreme pressure additives and mineral oils either will not emulsify or will form inferior emulsions that break when stored or used. Then too, the more stable sulfurized products would not perform well because they did not release their sulfur under conditions of high temperature and pressure to provide essential EP lubrication.
Accordingly, it is a principal object of this invention to provide a series of novel polyoxyalkylene bis-thiourea extreme pressure agents and process for their manufacture.
Another principal object is to provide metal-working compositions comprising the bis-thiourea EP agents which possess good stability and shelf-life, but nevertheless release their sulfur to form protective films under conditions of high temperature and pressure.
Another object is to provide complete aqueous base metal working compositions for use under extreme conditions during heavy duty machining operations.
A still further object of the present invention is to provide a method of machining under conditions of extreme pressure and temperature with polyoxyalkylene bis-thiourea EP agents.
These and other objects, features and advantages of this invention will become apparent to those skilled in the art after a reading of the following more detailed description.
SUMMARY OF THE INVENTION As stated above, this invention relates to novel and useful thioureas. In particular, it is concerned with thioureas having their terminal nitrogens substituted and unsubstituted which can be represented by the following formula:
wherein x, R, R and Y are as defined above. Their molecular weights are generally under 1000 and in most instances will range fromabout 250 to 950. Each of the Rs may be hydrogen, but are preferably substituted with alkyl or alkenyl. When alkyl or alkenyl, they are advantageously 1 to 8 carbon atoms, which includes lower alkyl radicals of l to 3 or 4 carbon atoms such as methyl, ethyl and propyl as well as lower alkenyls like ethylene, propenyl and allyl. These groups also include higher alkyls and alkenyls usually up to 8 carbon atoms, however, lower members are preferred for better water solubility. The above formula contemplates in addition to normal aliphatic radicals their usual isomeric forms such as iso-propyl, butyl, secondary and tertiary butyl and the like. Y may be hydrogen, however, here too in most instances it will be lower alkyl of l to 3 carbon atoms like methyl, ethyl and propyl.
In the above formula, x is a number from 1 to 10 with an intermediate preferred range from about 3 to 6. Thioureas in which x is about 3 and 5.6 have been specially advantageous.
Specific examples of a few of the thioureas contemplated within the instant invention are represented in the following table.
Generally, the process for their preparation involves reacting a polyether diamine with an isothiocyanate. The reaction mixture is heated for several hours forming a homogeneous solution. The mixture is then treated to remove the solvent used to dissolve the reactants.
Broadly, the polyether diamine reactant of this invention is a polyoxyalkylene diamine. It encompasses both linear and branched members having at least one and preferably a plurality of ether linkages and containing two terminal primary amino groups. Their molecular weights generally range from about 100 to 700. These polyethers are substantially free from functional groups other than amino. They may have the following formula:
rated-by-reference herein. Polyethers of the kind described above are available under the trademark Jeffamine by Jefferson Chemical.
Alternatively, similar other amines of the following structure can be used:
f \CI-h/a O CH3 0/x \CHz/3 NHz wherein Y is hydrogen or lower alkyl of 1 to 3 carbon atoms and x is a number from 1 to 10. A preferred illustrative example of such glycol diamines is di-(3-aminopropyl) ether of dipropylene glycol having the formula:
A These polyether diamines and process for their manufacture are taught in U.S. Pat. 3,316,185 which disclosure is incorporated-by-reference herein.
Isothiocyanates are reacted with the polyether diamines to form the adduct. Those isothiocyanates for use in the propyl) ether of dipropylene glycol having the formula:
wherein Z is hydrogen, alkyl or alkenyl. When Z is alkyl or alkenyl, they are radicals of 1 to 8 carbon atoms corresponding with the aforementioned R substituents. Illustrative examples of specific isothiocyanates are isothiocyanic acid and their corresponding esters such as methyl, ethyl, propyl, allyl, isopropyl and the like.
Before charging the reaction vessel, the reactants are separately dissolved in virtually any appropriate organic solvent such as benzene, acetone, toluene, xylene, various ethers like diethyl, methyl ethyl ethers as well as various alcohols such as methyl, ethyl, isopropyl, etc. The polyether amine reactant is preferably cooled below ambient temperature to compensate for the exotherm produced from mixing the reactants. Here, specific cooling temperatures are not critical but remain a factor based upon the rate at which the isothiocyanate and polyether are added together. Accordingly, the reactants should be slowly incorporated to avoid excessive heat build-up from the exothermic reaction. In most cases, the mole ratio for the reactants is about 2 moles of the isothiocyanate for each mole of the polyether diamine.
The reaction mixture is then heated, preferably under reflux conditions which are at temperatures in the range from 65 to 95 C. and more specifically at about C. Heating should be continuous for several hours until a homogeneous solution forms which in most instances is water white to straw yellow in color. Solvents initially used to dissolve the reactants are then removed. This can be accomplished by several means, but most conveniently by stripping the mixture at reduced temperatures and pressures. The temperature is lowered to about 40 to 80 C. and the pressure reduced to 30 to 50 mm. Hg. Ordinarily, a solvent free product can be secured in about 1- /2 to 3 hours. The final polyoxyalkylene bis-thiourea is H'IN ' a glassy clear to light yellow liquid.
The polyoxyalkylene bis-thiourea extreme pressure lubricants of the present invention act by forming protective metal sulfides on the surface of the workpiece under extreme temperatures and pressures. However, optimal results can best be achieved if these EP agents are used in conjunction with boundary lubricants and specially polar type boundary lubricants. In the case of the latter, their polar ends, which may be the fatty acid or ester portion of the molecule, are absorbed onto the metal surface forming a film, and the non-polar portions provide added strength to the film through cohesion.
Preferred boundary lubricants include long chained aliphatic acid soaps having 8 to 22. carbon atoms in their acid moiety. The cationic moiety may be an alkali metal such as sodium potassium, lithium and ammonium. Others include morpholine, mono, diand tri-ethanolamines,
0 R-ii-o-(X)-o oH,oH,-0
wherein R is a saturated, unsaturated, branched or unbranched chain having 7 to 21 carbon atoms, X corresponds to R, however, the former have chains of 2 to 16 carbon atoms containing one or more hydroxyl groups and n is 1 to 20. Included in this group are products available under the trademark Ethofat by Armour.
Other boundary lubricants for use in accordance with the instant invention are ethoxylated aliphatic or olefinic alcohols of the formula:
wherein x and y are numbers from 1 to 20. R represents 30 carbon atoms and n is 1 to 20. This group includes ethoxylated cetyl, stearyl or oleyl alcohols having moles of ethylene oxide. Others are the polyoxyethylene substituted N,N' fatty acid amides available under the trademark Ethomid by Armour.
Additional agents useful in the instant compositions are ethoxylated amines of the formula:
wherein x and y are numbers from 1 to 20. R represents salts and aliphatic or olefinic acids of these amines having 8 to 22 carbon atoms such as oleic and stearic acid. They are sold by Armour under the trademark Ethomeen.
Specific preferred products are the C/15, C/ and C/ formulations. Further related products include ethoxylated diamines, salts and acids thereof which can also be employed with the thiourea EP agents. They include the Ethoduomeen line by Armour.
The present invention also contemplates compositions containing lower alkyl and natural esters of C to C fatty acids such as methyl lardate, ethyl linoleate and methyl tallate.
Generally, EP lubricants of the present invention are used in an amount sufficient to provide anti-weld properties. Though not required in each instance, it is advantageous to employ in complete compositions the aforementioned boundary lubricants in an amount suflicient to enhance or activate the performance of the EP agent. The ratio of EP agent to boundary lubricant is used in the range from about 1:1 to 1:30. The combined concentration of EP agent and boundary lubricant in formulations should be from 2% to 85%, and when diluted for use, should have a concentration ranging from about 0.03% to 5% and preferably about 0.1% to 3.0%.
The extreme pressure agents of this invention can be formulated into numerous metal working compositions by incorporating the ingredients together using conventional, known techniques. The compositions will ordinarily be in the form of solutions and emulsions.
Complete metal working compositions are those containing usual base cutting fluids, and preferably for purposes of the instant invention aqueous base metal-working fluids. Aqueous type fluids are those containing water or are diluted with water prior to use. Aqueous base fluids may be of the soluble oil type which are water emulsifiable, and contain mineral oils as well as emulsifiers. Emulsifiers commonly used therewith may be the mahogany soaps, conventional soaps, rosin acid and tall oil soaps. Any number of nonionic and anionic surfactants such as sodium lauryl sulfate, including the phenolate, carboxylate, sulfonate surfactants and the like can be used with soluble oils.
Compositions of this invention may also contain other adjuvants frequently used in metal working fluids such as coupling agents, anti-foam agents, corrosion inhibitors, bactericides, wetting agents, etc. Typical coupling agents are the glycol ethers available under the trademark Cellosolve which includes their methyl, ethyl and butyl homologues. Other such agents include butyl and amyl alcohol, various polyols and mixtures thereof.
Corrosion and rust inhibitors such as borax, sodium nitrite, alkanolamines like diand tri-ethanolamines and condensation products of diethanolamine with fatty acids are frequently used. Anti-foam agents include conventional agents such as ester waxes, fatty acid esters of higher alcohols such as methyl stearate and tricresyl phosphate. Agents like O-phenol phenoxide, methyl p-hydroxy benzoate and quaternary amines such as Dowicil act to stabilize fluids against fungal or bacterial growth. The specific combination of additives used and their proportional range or ratio in each case will naturally vary depending on the kind of machining undertaken, the type of metal and operation, whether it is light, medium or heavy duty cutting, grinding, milling, broaching, or whatever.
The polyoxyalkylene bis-thioureas can be used in a broad range of heavy-duty machining processes. Machining for purposes of this invention relates to all types of cutting and grinding on a general basis. There are no special limitations in their use, but can be employed whenever special lubrication is indicated. The workpiece is contacted with the fluid by any conventional method. Ordinarily, in the case of small bench and lathe work, manual methods can be used such as brush, roller or hand squirt can applicators. However, for larger floorstand production machines, pump pressure circulation, bath or jet spray methods will ordinarily be employed.
The following examples illustrate some of the embodiments of this invention. It is to be understood that these are for illustrative purposes only and do not purport to be wholly definitive as to conditions and scope.
A 500 ml. four-neck round bottom flask fitted with a stirrer, thermometer, condenser and addition funnel was charged with 52.1 grams of a polyether diamine having the following formula:
and dissolved in ml. of isopropyl alcohol. In a second flask, 37 grams of methyl isothiocyanate was dissolved in 75 ml. of isopropyl alcohol. The dissolved methyl isothiocyanate was slowly added to the dissolved polyether over a 45 minute period with stirring. During this time, a slight exotherm occurred. After the addition was completed, the reaction mixture was refluxed at the boiling point of the isopropyl alcohol and allowed to stand overnight. On the following day, the solvent was removed by means of a rotating vacuum evaporator. Evaporation was performed at 6070 C. and at approximately 30 mm. Hg pressure. The final product had the appearance of a clear oil.
The above product was prepared according to the method of Example I, however, the polyether diamine starting material had a molecular weight of 230 and x was 2.6.
EXAMPLE III Wt. percent EP agent of Example I 4.00 Methyl lardate 7.50 Parafiin oil 64.00 Butyl Cellosolve 2.00 Sodium petroleum sulfonate 22.00 Methyl p-hydroxybenzoate 0.50
A kettle was charged with the EP agent, butyl Cellosolve, methyl lardate, methyl p-hydroxybenzoate and sodium petroleum sulfonate. The ingredients were warmed to 120 to 140 F. and blended until uniform at which time the paraffin oil was finally added with stirring.
EXAMPLE IV Wt. percent EP agent of Example I 1.00 Butyl Cellosolve 1.00 Ethofat 242/25 6.00 Triethanolamine 10.00 Bactericide (Dowicil 100) 0.50 Water 81.50
All ingredients were charged to an open kettle except the water. The composition was stirred until uniform. The water was then added to the kettle.
The mineral oil and petroleum sulfonate salt were added to an open head kettle. The EP agent and methyl lardate were then blended into the mineral oil-sodium petroleum sulfonate solution. Finally, the Dowicil 100- water-butyl Cellosolve was added as a pre-blend. The blending was carried out at a temperature in the range of 100 to 140 F.
While the invention has been described in conjunction with specific examples thereof, this is illustrative only. Accordingly, many alternatives, modification and variations will be apparent to those skilled in the art in light of the foregoing description, and it is therefore intended to embrace all such alternatives, modifications and variations as to fall within the spirit and broad scope of the appended claims.
We claim:
1. A method of machining a metallic workpiece under conditions of high temperature and pressure, which method comprises contacting the workpiece with a metal working composition comprising a lubricating base containing extreme pressure improving amounts of a compound of the formula:
wherein R and R are selected from the group consisting of hydrogen, alkyl and alkenyl, Y is hydrogen or lower alkyl and x is a number from 1 to 10.
2. The method of claim 1 wherein the metal working composition comprises a compound wherein R and R are methyl, Y is methyl and x is a number from about 3 to 6.
3. The method of claim 1 wherein the metal working composition comprises a compound wherein R and R are ethyl, Y is methyl and x is a number from about 3 to 6.
4. A metal working composition comprising a major amount of an aqueous lubricating base and a minor amount of a compound of the following formula sufiicient to impart extreme pressure properties to said composition:
wherein R and R are selected from the group consisting of hydrogen alkyl and alkenyl in which alkyl and alkenyl have up to 8 carbon atoms, Y is hydrogen or lower alkyl and x is a number from 1 to 10.
5. The composition of claim 4 wherein R and R of the extreme pressure agent are methyl, Y is methyl and x is a number from about 3 to 6.
6. The composition of claim 4 wherein R and R of the extreme pressure agent are ethyl, Y is methyl and x is a number from about 3 to 6.
References Cited UNITED STATES PATENTS 3,704,321 11/1972 Kmet et al. 260-552 R 3,579,449 5/1971 Wann et al. 25249.5 3,584,993 1/1971 Myles et al. 25247.5
WARREN H. CANNON, Primary Examiner US. Cl. X.R. 25249.5
US00289203A 1971-05-24 1972-09-14 Polyoxyalkylene bis-thiourea extreme pressure agents and methods of use Expired - Lifetime US3798164A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US14653571A 1971-05-24 1971-05-24
US28920372A 1972-09-14 1972-09-14

Publications (1)

Publication Number Publication Date
US3798164A true US3798164A (en) 1974-03-19

Family

ID=26844029

Family Applications (2)

Application Number Title Priority Date Filing Date
US146535A Expired - Lifetime US3704321A (en) 1971-05-24 1971-05-24 Polyoxyalkylene bis-thiourea extreme pressure agents and methods of use
US00289203A Expired - Lifetime US3798164A (en) 1971-05-24 1972-09-14 Polyoxyalkylene bis-thiourea extreme pressure agents and methods of use

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US146535A Expired - Lifetime US3704321A (en) 1971-05-24 1971-05-24 Polyoxyalkylene bis-thiourea extreme pressure agents and methods of use

Country Status (1)

Country Link
US (2) US3704321A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3901815A (en) * 1974-06-05 1975-08-26 Texaco Inc Synthetic aircraft turbine oil
DE2734906A1 (en) * 1976-08-04 1978-02-09 Singer & Hersch Industrial Dev AQUEOUS LIQUID OR CONCENTRATE, METHOD FOR THE PRODUCTION AND USE THEREOF
US4313837A (en) * 1980-05-02 1982-02-02 Amax, Inc. Using molybdates to inhibit corrosion in water-based metalworking fluids
US4326974A (en) * 1980-09-12 1982-04-27 Swiss Aluminium Ltd. Oil-in-water emulsion for cold rolling light metals
US4447348A (en) * 1981-02-25 1984-05-08 The Lubrizol Corporation Carboxylic solubilizer/surfactant combinations and aqueous compositions containing same
US4448703A (en) * 1981-02-25 1984-05-15 The Lubrizol Corporation Carboxylic solubilizer/surfactant combinations and aqueous compositions containing same
US4666620A (en) * 1978-09-27 1987-05-19 The Lubrizol Corporation Carboxylic solubilizer/surfactant combinations and aqueous compositions containing same
US4770803A (en) * 1986-07-03 1988-09-13 The Lubrizol Corporation Aqueous compositions containing carboxylic salts
USRE36479E (en) * 1986-07-03 2000-01-04 The Lubrizol Corporation Aqueous compositions containing nitrogen-containing salts

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3879305A (en) * 1973-03-26 1975-04-22 Mobil Oil Corp Grease thickened with oxygen-linked or sulfur-linked polyureas
US4154724A (en) * 1976-06-28 1979-05-15 Texaco Development Corp. Polyether polyureides and resinous compositions therefrom
US4261845A (en) * 1980-01-18 1981-04-14 Texaco Development Corporation Novel polyureas and their use as grease thickening agents
US6187726B1 (en) * 1999-11-12 2001-02-13 Ck Witco Corporation Substituted linear thiourea additives for lubricants

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3901815A (en) * 1974-06-05 1975-08-26 Texaco Inc Synthetic aircraft turbine oil
DE2734906A1 (en) * 1976-08-04 1978-02-09 Singer & Hersch Industrial Dev AQUEOUS LIQUID OR CONCENTRATE, METHOD FOR THE PRODUCTION AND USE THEREOF
US4666620A (en) * 1978-09-27 1987-05-19 The Lubrizol Corporation Carboxylic solubilizer/surfactant combinations and aqueous compositions containing same
US4313837A (en) * 1980-05-02 1982-02-02 Amax, Inc. Using molybdates to inhibit corrosion in water-based metalworking fluids
US4326974A (en) * 1980-09-12 1982-04-27 Swiss Aluminium Ltd. Oil-in-water emulsion for cold rolling light metals
US4447348A (en) * 1981-02-25 1984-05-08 The Lubrizol Corporation Carboxylic solubilizer/surfactant combinations and aqueous compositions containing same
US4448703A (en) * 1981-02-25 1984-05-15 The Lubrizol Corporation Carboxylic solubilizer/surfactant combinations and aqueous compositions containing same
US4770803A (en) * 1986-07-03 1988-09-13 The Lubrizol Corporation Aqueous compositions containing carboxylic salts
USRE36479E (en) * 1986-07-03 2000-01-04 The Lubrizol Corporation Aqueous compositions containing nitrogen-containing salts

Also Published As

Publication number Publication date
US3704321A (en) 1972-11-28

Similar Documents

Publication Publication Date Title
US3933658A (en) Metalworking additive and composition
CA1076545A (en) Water-based hydraulic fluid
US4151099A (en) Water-based hydraulic fluid and metalworking lubricant
US3798164A (en) Polyoxyalkylene bis-thiourea extreme pressure agents and methods of use
US3897349A (en) Anti-rust additive composition
US2825693A (en) Metal working lubricant
US4312768A (en) Synergistic polyether thickeners for water-based hydraulic fluids
US4209414A (en) Dual-purpose hydraulic fluid
US4419252A (en) Aqueous lubricant
CA2938598C (en) Polyalkanoic or polyalkenoic acid based high perormance, water-dilutable lubricity additive for multi-metal metalworking applications
KR850001965B1 (en) Aqueous functional fluid composition
JPS6043395B2 (en) Metal machining method and lubricant concentrate used therein
US4289636A (en) Aqueous lubricant compositions
JPS61141793A (en) Lubricant composition for sliding and metal working and lubrication of machine tool using same
EP0183050B1 (en) Lubricating additive
EP0122528A2 (en) Thickened, water-based hydraulic fluid with reduced dependence of viscosity on temperature
CA1152976A (en) Water-based hydraulic fluid containing an alkyl dialkanolamide
US3657123A (en) Lubricant compositions
US2780598A (en) Metal working and liquid coolants therefor
JP2530633B2 (en) Aqueous system containing the reaction product of hydrocarbyl-substituted succinic acid and / or anhydride with amine-terminated poly (oxyalkylene) and ibid.
US4218329A (en) Cooling and lubricating fluid for metal working
US4670168A (en) Aqueous metal removal fluid
US4259206A (en) Metal working lubricant containing an alkanolamine and a cycloaliphatic acid
EP0061823B1 (en) Synergistically thickened water-based hydraulic or metal-working fluid
EP0192358A2 (en) Metal working fluid composition