USRE33658E - Lubricants for reciprocating air compressors - Google Patents
Lubricants for reciprocating air compressors Download PDFInfo
- Publication number
- USRE33658E USRE33658E US07/370,356 US37035689A USRE33658E US RE33658 E USRE33658 E US RE33658E US 37035689 A US37035689 A US 37035689A US RE33658 E USRE33658 E US RE33658E
- Authority
- US
- United States
- Prior art keywords
- weight percent
- carbon atoms
- composition
- ester
- effective amount
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M111/00—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
- C10M111/04—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/36—Esters of polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/20—Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
- C10M107/30—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M107/32—Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
- C10M107/34—Polyoxyalkylenes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
- C10M171/008—Lubricant compositions compatible with refrigerants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
- C10M2207/2825—Esters of (cyclo)aliphatic oolycarboxylic acids used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/285—Esters of aromatic polycarboxylic acids
- C10M2207/2855—Esters of aromatic polycarboxylic acids used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/1033—Polyethers, i.e. containing di- or higher polyoxyalkylene groups used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
- C10M2209/1045—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
- C10M2209/1055—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/106—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing four carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/106—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing four carbon atoms only
- C10M2209/1065—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing four carbon atoms only used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/107—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/107—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106
- C10M2209/1075—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106 used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/108—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
- C10M2209/1085—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/109—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
- C10M2209/1095—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
- C10M2215/065—Phenyl-Naphthyl amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/221—Six-membered rings containing nitrogen and carbon only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/223—Five-membered rings containing nitrogen and carbon only
- C10M2215/224—Imidazoles
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
- C10M2215/226—Morpholines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/30—Heterocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/043—Ammonium or amine salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/06—Instruments or other precision apparatus, e.g. damping fluids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/30—Refrigerators lubricants or compressors lubricants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/32—Wires, ropes or cables lubricants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/34—Lubricating-sealants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/36—Release agents or mold release agents
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/38—Conveyors or chain belts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/40—Generators or electric motors in oil or gas winning field
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/42—Flashing oils or marking oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/44—Super vacuum or supercritical use
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/50—Medical uses
Definitions
- This invention relates to synthetic lubricants which are a suitably inhibited blend of (1) an ester of a monohydric alcohol having 4 to 18 carbon atoms with one or more aromatic or alkane dicarboxylic acids and (2) one or more polyether polyols.
- Anderol 495 sold by Nuodex for rotary screw air compressors.
- the major component of Anderol 495 is believed to be a dialkyl adipate.
- Anderol 495 does not have sufficient high temperature viscosity for suitable lubrication of the pistons and cylinders of reciprocating air compressors.
- Anderol 500 (a dialkyl phthalate composition) is known to be useful in reciprocating air compressors.
- this synthetic ester has the disadvantage of having a high viscosity during start up at low temperatures.
- Synthetic lubricants comprising a major amount of a polyester and a minor amount of a monocapped polyglycol are known from British Pat. Nos. ,933,721; 986,066; and 1,162,818, however all these compositions are disclosed to be only useful in aircraft gas turbines where a different viscosity range is needed.
- esters of aliphatic monohydric alcohols with one or more aromatic or alkane dicarboxylic acids have the required high temperature viscosity and stability to heat, air, and water.
- the synthetic base lubricants of this invention comprise a lubricant composition comprising,
- R 1 is an alkylene radical having 2 to 4 carbon atoms
- n is a number having an average value which will give a number average molecular weight range from about 400 to about 5000 for the final compound
- n is an integer having a value of from 1 to about 8
- R 2 is hydrogen or an alkyl group of 1 to 6 carbon atoms.
- An additional aspect of the present invention comprises the above base lubricant with the addition of effective amounts of oxidation inhibitors, corrosion inhibitors, and metal or copper deactivators and a method of lubricating air compressors using the inhibited lubricant.
- the neutral esters used in this invention are commercially available.
- suitable esters are the esters of monohydric alcohols having 4 to 18 carbons such as butanol, octanol, decanol, etc with aromatic dicarboxylic acids such as phthalic, terephthalic and isophthalic acids.
- esters of the above monohydric alcohols with alkanedioic acids having 4 to 18 carbons such as succinic, adipic, suberic, tetradecane 1,14-dioic acid, and hexadecane-1,16-dioic acid,
- polyether polyols or polyoxyalkylene polyols used in this invention are those derived from ethylene oxide, propylene oxide, 1-2, or 2-3 butylene oxide.
- the above oxides may be polymerized alone, i.e., homopolymerized or in combination.
- the combined oxides may also be combined in a random or block addition. While some of the above compounds may be of a hydrophilic nature, those of a hydrophobic nature are preferred, such as those derived from propylene oxide, butylene oxides or combinations thereof.
- Suitable capped polyoxyalkylene glycols are those derived from ethylene, propylene, and butylene oxides wherein the alkylene oxides are initiated from a compound having 1 to 8 active hydrogens in a known manner.
- the terminal hydroxyl groups may be further reacted with organic acids to form esters or with alkyl or aryl halides to form alkyl or aryl capped polyoxyalkylene are well known from the book "Polyurethanes" by Saunders and Frisch, Interscience Publishers (1962), pages 33-39. This book is incorporated by reference herein.
- Suitable initiator compounds which are employed to prepare the above polyether polyols are compounds having 1-8 active hydrogens such as for example water, methanol, ethanol, propanol, butanol, ethylene glycol, propylene, glycol, butylene glycol, 1,6-hexane diol, glycerine, trimethylolpropane, pentaerythritol, sorbitol, sucrose, mixtures thereof and the like.
- initator compounds which are useful include monohydric phenols and dihydric phenols and their alkylated derivatives such as phenol, o, m, and p cresol, guaiacol, saligenin, carvacrol, thymol, o and p -hydroxy diphenyl, catechol, resorcinol, hydroquinone, pyrogallol, and phloroglucinol.
- polyether polyols should have a flash point greater that 375° F. (191° C.) and preferably greater than 450° F. (232° C.). They also should have a number average molecular weight range from about 400 to 5000 and preferably in the range 700 to 2500.
- the foregoing polyether polyols are blended to give a base lubricant composition containing 15 to 45 weight percent of the esters and 85 to 55 weight percent of the polyols with the ranges 15 to 25 and 85 to 75 being the preferred ranges, respectively.
- compositions of this invention are used in a reciprocating air compressor and are selected so as to have a viscosity in the range of 5 to 25 centistokes at 210° F. (99° C.) and preferably 6 to 16 centistokes at 210° F. (99° C.) and a pour point in the range of 0° to -65° F. (18° to -54° C.).
- the final lubricant compositions of this invention may contain effective amounts of ashless additives, such as antioxidants, corrosion inhibitors, metal deactivators, lubricity additives, extreme pressure additives, dispersants, detergents, demulsifiers or such additives as may be required.
- ashless additives such as antioxidants, corrosion inhibitors, metal deactivators, lubricity additives, extreme pressure additives, dispersants, detergents, demulsifiers or such additives as may be required.
- antioxidants examples include phenyl naphthylamines, i.e., both alpha and beta-naphthyl amines; diphenyl amine; iminodibenzyl; p,p-dibutyl-diphenylamine; p,p'-dioctyldiphenylamine; and mixtures thereof.
- Other suitable antioxidants are hindered phenolics such as 6-t-butylphenol, 2,6-di-t-butylphenol and 4-methyl-2,6-di-t-butylphenol and the like.
- ashless metal corrosion inhibitors are commercially available, such as Irgalube 349 from Ciba-Geigy. This inhibitor compound is an aliphatic amine salt of phosphoric acid monohexyl ester.
- Other useful metal corrosion inhibitors are NA-SUL DTA and Na-SUL EDS from the White Chemical Company (diethylenetriamine dinonylnapthalene sulfonate and ethylene diamine dimonylnaphthalene sulfonate), respectively.
- ashless cuprous metal deactivators examples include imidazole, benzimidazole, pyrazole, benzotriazole, tolutriazole, 2-methyl benzimidazole, 3,5-dimethyl pyrazole, and methylene bis-benzotriazole.
- An effective amount of the foregoing additives for use in a reciprocating air compressor is generally in the range from 0.1 to 5% by weight for the antioxidants, 0.1 to 5.0% by weight for the corrosion inhibitors, and 0.001 to 0.5 percent by weight for the metal deactivators.
- the foregoing weight percentages are based on the total weight of the polyether polyols and the esters. It is to be understood that more or less of the additives may be used depending upon the circumstances for which the final composition is to be used.
- the ester and additives were blended together. After sufficient agitation time, the ester/additive mixture was transferred to the vessel which holds the polyglycol. The mixture was heated to 80° C. and agitated until the solution was clear. If the additives are ignored, the formulation contains 20% by weight of the ester and 80% by weight of the polypropylene glycol.
- the above fluid was tested for corrosion resistance in accordance with ASTM D-665--procedure A and ASTM D-665--procedure B. The fluid passed both tests.
- the above fluid was placed in fourteen reciprocating air compressors made by different manufacturers.
- the valves in each compressor were checked intermittently over a long period of time as shown in the table.
- the valves were found to be in excellent condition having no deposits or residues.
- the same compressors using petroleum oils have service deposits after 1000 to 4000 hours of operation which create reduced performance with the possibility of line fires.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Lubricants (AREA)
Abstract
Synthetic lubricants comprising 15 to 45 weight percent of an ester of a monohydric alcohol of 4 to 18 carbon atoms with one or more aromatic or alkane dicarboxylic acids having 4 to 18 carbon atoms blended with 85 to 55 weight percent of one or more polyether polyols having a number average molecular weight from about 400 to 5000. The blends are compounded with antioxidants, corrosion inhibitors, and metal deactivators to produce a superior lubricant for reciprocating air compressors which gives a long life to the compressors.
Description
This application is a continuation-in-part of Ser. No. 812,167 filed Dec. 23, 1985, now abandoned.
This invention relates to synthetic lubricants which are a suitably inhibited blend of (1) an ester of a monohydric alcohol having 4 to 18 carbon atoms with one or more aromatic or alkane dicarboxylic acids and (2) one or more polyether polyols.
Reciprocating air compressors having air cushioned valves are well known in the art.
It is well known to use hydrocarbon lubricating oils to lubricate the pistons and piston rings of the foregoing air compressors and lubricate the bearings. Due to the high temperature and pressure of the air, it has been found that these hydrocarbon oils break down, leave deposits, and prevent the valves from operating correctly in a relatively short time. This requires manual repairs to clean the valves.
It is known that synthetic esters made from dicarboxylic acids have been used to produce long lasting compressor fluids, such as Anderol 495 sold by Nuodex for rotary screw air compressors. The major component of Anderol 495 is believed to be a dialkyl adipate. However, Anderol 495 does not have sufficient high temperature viscosity for suitable lubrication of the pistons and cylinders of reciprocating air compressors.
It is also known from U.S. Pat. No. 4,302,343 that rotary screw air compressors can be lubricated with a blend of polyhydric alcohol esters and polyether polyols. However, these lubricants are relatively expensive and leave deposits on the valves of a reciprocating air compressor.
Anderol 500 (a dialkyl phthalate composition) is known to be useful in reciprocating air compressors. However, this synthetic ester has the disadvantage of having a high viscosity during start up at low temperatures.
The U.S. Pat. No. 4,072,619 polyesteralkylene glycol compositions are disclosed wherein phenothiazine is incorporated into the alkylene glycols. However, these compositions have been found to degrade in a relatively short time i.e. 1000 hours.
Synthetic lubricants comprising a major amount of a polyester and a minor amount of a monocapped polyglycol are known from British Pat. Nos. ,933,721; 986,066; and 1,162,818, however all these compositions are disclosed to be only useful in aircraft gas turbines where a different viscosity range is needed.
It now has been found that a suitably inhibited blend of esters of aliphatic monohydric alcohols with one or more aromatic or alkane dicarboxylic acids have the required high temperature viscosity and stability to heat, air, and water.
More specifically, the synthetic base lubricants of this invention comprise a lubricant composition comprising,
(A) about 15 to 45 weight percent of an ester of a monohydric alcohol having 4 to 18 carbon atoms with one or more aromatic or alkane dicarboxylic acids having 4 to 18 carbon atoms, and
(B) about 85 to 55 weight percent of one or more polyether polyols have a flash point greater than 375° F. (191° C.) and which have the formula
Z--[(--R.sup.1 O).sub.n R.sup.2 ].sub.m
where Z is the residue of a compound having 1-8 hydroxyl groups,
R1 is an alkylene radical having 2 to 4 carbon atoms,
n is a number having an average value which will give a number average molecular weight range from about 400 to about 5000 for the final compound,
m is an integer having a value of from 1 to about 8,
R2 is hydrogen or an alkyl group of 1 to 6 carbon atoms.
An additional aspect of the present invention comprises the above base lubricant with the addition of effective amounts of oxidation inhibitors, corrosion inhibitors, and metal or copper deactivators and a method of lubricating air compressors using the inhibited lubricant.
The neutral esters used in this invention are commercially available. Examples of suitable esters are the esters of monohydric alcohols having 4 to 18 carbons such as butanol, octanol, decanol, etc with aromatic dicarboxylic acids such as phthalic, terephthalic and isophthalic acids.
Also useful are the esters of the above monohydric alcohols with alkanedioic acids having 4 to 18 carbons such as succinic, adipic, suberic, tetradecane 1,14-dioic acid, and hexadecane-1,16-dioic acid,
Examples of the polyether polyols or polyoxyalkylene polyols used in this invention are those derived from ethylene oxide, propylene oxide, 1-2, or 2-3 butylene oxide. The above oxides may be polymerized alone, i.e., homopolymerized or in combination. The combined oxides may also be combined in a random or block addition. While some of the above compounds may be of a hydrophilic nature, those of a hydrophobic nature are preferred, such as those derived from propylene oxide, butylene oxides or combinations thereof.
Examples of suitable capped polyoxyalkylene glycols are those derived from ethylene, propylene, and butylene oxides wherein the alkylene oxides are initiated from a compound having 1 to 8 active hydrogens in a known manner. The terminal hydroxyl groups may be further reacted with organic acids to form esters or with alkyl or aryl halides to form alkyl or aryl capped polyoxyalkylene are well known from the book "Polyurethanes" by Saunders and Frisch, Interscience Publishers (1962), pages 33-39. This book is incorporated by reference herein.
Examples of suitable initiator compounds which are employed to prepare the above polyether polyols are compounds having 1-8 active hydrogens such as for example water, methanol, ethanol, propanol, butanol, ethylene glycol, propylene, glycol, butylene glycol, 1,6-hexane diol, glycerine, trimethylolpropane, pentaerythritol, sorbitol, sucrose, mixtures thereof and the like.
Other initator compounds which are useful include monohydric phenols and dihydric phenols and their alkylated derivatives such as phenol, o, m, and p cresol, guaiacol, saligenin, carvacrol, thymol, o and p -hydroxy diphenyl, catechol, resorcinol, hydroquinone, pyrogallol, and phloroglucinol.
The foregoing polyether polyols should have a flash point greater that 375° F. (191° C.) and preferably greater than 450° F. (232° C.). They also should have a number average molecular weight range from about 400 to 5000 and preferably in the range 700 to 2500.
The foregoing polyether polyols are blended to give a base lubricant composition containing 15 to 45 weight percent of the esters and 85 to 55 weight percent of the polyols with the ranges 15 to 25 and 85 to 75 being the preferred ranges, respectively.
The compositions of this invention are used in a reciprocating air compressor and are selected so as to have a viscosity in the range of 5 to 25 centistokes at 210° F. (99° C.) and preferably 6 to 16 centistokes at 210° F. (99° C.) and a pour point in the range of 0° to -65° F. (18° to -54° C.).
The final lubricant compositions of this invention may contain effective amounts of ashless additives, such as antioxidants, corrosion inhibitors, metal deactivators, lubricity additives, extreme pressure additives, dispersants, detergents, demulsifiers or such additives as may be required.
Examples of useful ashless antioxidants which can be used herein are phenyl naphthylamines, i.e., both alpha and beta-naphthyl amines; diphenyl amine; iminodibenzyl; p,p-dibutyl-diphenylamine; p,p'-dioctyldiphenylamine; and mixtures thereof. Other suitable antioxidants are hindered phenolics such as 6-t-butylphenol, 2,6-di-t-butylphenol and 4-methyl-2,6-di-t-butylphenol and the like.
Examples of suitable ashless metal corrosion inhibitors are commercially available, such as Irgalube 349 from Ciba-Geigy. This inhibitor compound is an aliphatic amine salt of phosphoric acid monohexyl ester. Other useful metal corrosion inhibitors are NA-SUL DTA and Na-SUL EDS from the White Chemical Company (diethylenetriamine dinonylnapthalene sulfonate and ethylene diamine dimonylnaphthalene sulfonate), respectively.
Examples of suitable ashless cuprous metal deactivators are imidazole, benzimidazole, pyrazole, benzotriazole, tolutriazole, 2-methyl benzimidazole, 3,5-dimethyl pyrazole, and methylene bis-benzotriazole.
An effective amount of the foregoing additives for use in a reciprocating air compressor is generally in the range from 0.1 to 5% by weight for the antioxidants, 0.1 to 5.0% by weight for the corrosion inhibitors, and 0.001 to 0.5 percent by weight for the metal deactivators. The foregoing weight percentages are based on the total weight of the polyether polyols and the esters. It is to be understood that more or less of the additives may be used depending upon the circumstances for which the final composition is to be used.
The following preparation and examples are presented to illustrate but not limit the invention.
A formulation consisting of the following blend was prepared
(A) 11,489 pounds 5211.4 kg (77.48%) of polypropylene glycol (number average molecular weight 1200)
(B) 2,872 pounds 1302.7 kg (19.37%) of Mobil Ester DB-32(1)
(C) 296 pounds 134.3 kg (2.0%) of p,p'-dioctyl diphenylamine
(D) 148 pounds 67.1 kg (1.0%) of Ciba-Geigy IRGALUBE 349(2)
(E) 0.37 pounds 0.167 kg (25 parts per million) of Dow Corning DC-200(3)
(F) 15 pounds 6.8 kg (0.1%) of Mobil MOBILAD C-402(4)
(G) 7.4 pounds 3.35 kg (0.05%) of Sherwin-Williams CORBRATEC TT-100(5)
In a suitable vessel, the ester and additives were blended together. After sufficient agitation time, the ester/additive mixture was transferred to the vessel which holds the polyglycol. The mixture was heated to 80° C. and agitated until the solution was clear. If the additives are ignored, the formulation contains 20% by weight of the ester and 80% by weight of the polypropylene glycol.
The above fluid was tested for corrosion resistance in accordance with ASTM D-665--procedure A and ASTM D-665--procedure B. The fluid passed both tests.
The fluid was found to have the following characteristics:
______________________________________ Viscosity Temperature, (centistokes) ______________________________________ 210° F. (99° C.) 9.4 100° F. (38° C.) 59.3 0° F. (-18° C.) 3670 ______________________________________
The above fluid was placed in fourteen reciprocating air compressors made by different manufacturers. The valves in each compressor were checked intermittently over a long period of time as shown in the table. The valves were found to be in excellent condition having no deposits or residues. The same compressors using petroleum oils have service deposits after 1000 to 4000 hours of operation which create reduced performance with the possibility of line fires.
TABLE ______________________________________ Valve Discharge Hours of Temperature, Example Compressor Operation °F. (°C.) ______________________________________ 1 Ingersoll-Rand(XRE) 12,000 176(80) 2 Ingersoll-Rand(PRE) 12,000 208(98) 3 Ingersoll-Rand(XLE) 4,380 250(121) 4 Quincy intermittent 150(66) 5 Ingersoll-Rand(ES-1) 10,950 N/A 6 Chicago Pnuematic 14,500 280(138) 7 Chicago Pneumatic 9,850 280(138) 8 Ingersoll-Rand(ER-1) 5,330 N/A 9 Ingersoll-Rand(Type 30) 6,302 N/A 10 Ingersoll-Rand(Type 30) 1,144 N/A 11 Ingersoll-Rand(Type 30) intermittent 155(68) 12 Ingersoll-Rand(PRE) 11,260 270(132) 13 Ingersoll-Rand(PRE) 11,210 270(132) 14 Ingersoll-Rand(XLE) intermittent 360(182) ______________________________________ N/A = not available
Claims (12)
1. A lubricant composition comprising,
(A) about 15 to 45 weight percent of an ester of a monohydric alcohol having 4 to 18 carbon atoms with one or more aromatic .[.or alkane.]. dicarboxylic acids having 4 to 18 carbon atoms, and
(B) about 85 to 55 weight percent of one or more polyether polyols which have a flash point greater than 375° F. (191° C.) and which have the formula
Z--[(--R.sup.1 O).sub.n R.sup.2 ].sub.m
where
Z is the residue of a compound having 1-8 hydroxyl groups,
R1 is an alkylene radical having 2 to 4 carbon atoms,
n is a number having an average value which will give a number average molecular weight range from about 400 to about 5000 for the final compound,
m is an integer having a value of from 1 to about 8,
R2 is hydrogen or an alkyl group of 1 to 6 carbon atoms.
2. The lubricant composition of claim 1 wherein the weight percent of said ester ranges from 15 to 25 and the weight percent of said polyol ranges from 75 to 85. .[.3. A lubricant composition comprising,
(A) about 15 to 45 weight percent of an ester of a monohydric alcohol having 4 to 18 carbon atoms with one or more alkandioic acids having 4 to 18 carbon atoms, and
(B) about 85 to 55 weight percent of one or more polyoxyalkylene glycols having a flash point greater than 375° F. (191° C.) and having a number average molecular weight range from about 400 to 5000. .[.4. The lubricant composition of claim 3 wherein said polyoxyalkylene glycols are homopolymers..]. .[.5. The lubricant composition of claim 3 wherein said polyoxyalkylene glycols are random copolymers..]. .[.6. The lubricant composition of claim 3 wherein said polyoxyalkylene glycols are
block copolymers..]. 7. A lubricant composition comprising,
(A) about 15 to 45 weight percent of an ester of a monohydric alcohol with one or more aromatic dicarboxylic acids, and
(B) about 85 to 55 weight percent of one or more polyoxyalkylene glycols having a flash point greater than 375° F. and having a number
average molecular weight range from about 700 to 2500. 8. The lubricant composition of claim 7 wherein the weight percent of the ester ranges from 15 to 25 and the weight percent of the polyglycol ranges from 85 to 75.
The lubricant composition of claim 8 wherein the glycol is polypropylene glycol having a number average molecular weight of 1200.
The lubricant composition of claim 9 which comprises 20 weight percent
of said ester and 80 weight percent of said polypropylene glycol. 11. The composition of claim 1 which contains in addition
(A) an effective amount of an antioxidant,
(B) an effective amount of an ashless metal corrosion inhibitor, and
(C) an effective amount of a cuprous deactivator. 12. The composition of claim 1 which contains in addition
(A) about 0.1 to 5.0 weight percent of an aromatic amine antioxidant,
(B) about 0.1 to 2.0 weight percent of a ashless metal corrosion inhibitor, and
(C) about 0.001 to 0.5 weight percent of a cuprous metal deactivator. 13. The composition of claim 12 wherein said aromatic amine antioxidant is p,p'-dioctyl diphenyl amine, said ashless corrosion inhibitor is an amine salt of phosphoric acid monoester, and said cuprous metal deactivator is
tolutriazole. 14. A method of lubricating a reciprocating air compressor wherein said compressor is continuously run for long time intervals without downtime for valve maintenance which comprises using as the lubricant .[.the composition of claim 11.]. .Iadd.a composition comprising
(A) about 15 to 45 weight percent of an ester of an monohydric alcohol having 4 to 18 carbon atoms with one or more aromatic or alkane dicarboxylic acids having 4 to 18 carbon atoms,
(B) about 85 to 55 weight percent of one or more polyether polyols which have a flash point greater than 375° F. (191° C.) and which have the formula
Z--[(--R.sup.1 O).sub.n R.sup.2 ].sub.m
where Z is the residue of a compound having 1-8 hydroxyl groups, R1 is an alkylene radical having 2 to 4 carbon atoms, n is a number having an average value which will give a number average molecular weight range from about 400 to about 5000 for the final compound, m is an integer having a value of from 1 to about 8, R2 is hydrogen or an alkyl group of 1 to 6 carbon atoms,
(C) an effective amount of an antioxidant,
(D) an effective amount of an ashless metal corrosion inhibitor, and
(E) an effective amount of a cuprous deactivator.Iaddend.. 15. A method of lubricating a reciprocating air compressor wherein said compressor is continuously run for long time intervals without downtime for valve maintenance which comprises using as the lubricant .[.the composition of claim 12.]. .Iadd.a composition comprising
(A) about 15 to 45 weight percent of an ester of an monohydric alcohol having 4 to 18 carbon atoms with one or more aromatic or alkane dicarboxylic acids having 4 to 18 carbon atoms,
(B) about 85 to 55 weight percent of one or more polyether polyols which have a flash point greater than 375° F. (191° C.) and which have the formula
Z--[(--R.sup.1 O).sub.n R.sup.2 ].sub.m
where Z is the residue of a compound having 1-8 hydroxyl groups, R1 is an alkylene radical having 2 to 4 carbon atoms, n is a number having an average value which will give a number average molecular weight range from about 400 to about 5000 for the final compound, m is an integer having a value of from 1 to about 8, R2 is hydrogen or an alkyl group of 1 to 6 carbon atoms,
(C) about 0.1 to 5.0 weight percent of an aromatic amine antioxidant,
(D) about 0.1 to 2.0 weight percent of a ashless metal corrosion inhibitor, and
(E) about 0.001 to 0.5 weight percent of a cuprous metal
deactivator.Iaddend.. 16. A method of lubricating a reciprocating air compressor wherein said compressor is continuously run for long time intervals without downtime for valve maintenance which comprises using as the lubricant .[.the composition of claim 13.]. .Iadd.a composition comprising
(A) about 15 to 45 weight percent of an ester of an monohydric alcohol having 4 to 18 carbon atoms with one or more aromatic or alkane dicarboxylic acids having 4 to 18 carbon atoms,
(B) about 85 to 55 weight percent of one or more polyether polyols which have a flash point greater than 375° F. (191° C.) and which have the formula
Z--[(--R.sup.1 O).sub.n R.sup.2 ].sub.m
where Z is the residue of a compound having 1-8 hydroxyl groups, R1 is an alkylene radical having 2 to 4 carbon atoms, n is a number having an average value which will give a number average molecular weight range from about 400 to about 5000 for the final compound, m is an integer having a value of from 1 to about 8, R2 is hydrogen or an alkyl group of 1 to 6 carbon atoms,
(C) an effective amount of p,p'-dioctyl diphenyl amine,
(D) an effective amount of an amine salt of phosphoric acid monoester, and
(E) an effective amount of tolutriazole.Iaddend..
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/370,356 USRE33658E (en) | 1985-12-23 | 1989-06-22 | Lubricants for reciprocating air compressors |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US81216785A | 1985-12-23 | 1985-12-23 | |
US07/370,356 USRE33658E (en) | 1985-12-23 | 1989-06-22 | Lubricants for reciprocating air compressors |
Related Parent Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US81216785A Continuation-In-Part | 1985-12-23 | 1985-12-23 | |
US06/927,296 Reissue US4751012A (en) | 1985-12-23 | 1986-11-04 | Lubricants for reciprocating air compressors |
Publications (1)
Publication Number | Publication Date |
---|---|
USRE33658E true USRE33658E (en) | 1991-08-06 |
Family
ID=25208732
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/370,356 Expired - Lifetime USRE33658E (en) | 1985-12-23 | 1989-06-22 | Lubricants for reciprocating air compressors |
Country Status (2)
Country | Link |
---|---|
US (1) | USRE33658E (en) |
JP (1) | JPS62187799A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5225094A (en) * | 1991-12-18 | 1993-07-06 | Exxon Research And Engineering Company | Lubricating oil having an average ring number of less than 1.5 per mole containing a succinic anhydride amine rust inhibitor |
US6841522B2 (en) * | 1998-10-28 | 2005-01-11 | Imperial Chemical Industries Plc | Lubricant compositions |
CN111040848A (en) * | 2019-12-17 | 2020-04-21 | 魏平 | High-performance air compressor oil and preparation method thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0692591B2 (en) * | 1986-05-08 | 1994-11-16 | トヨタ自動車株式会社 | Synthetic lubricating oil composition for supercharger |
JP2744470B2 (en) * | 1989-06-09 | 1998-04-28 | 出光興産株式会社 | Lubricating oil composition |
Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB933721A (en) * | 1960-02-15 | 1963-08-14 | British Petroleum Co | Synthetic lubricants |
GB986066A (en) * | 1962-10-02 | 1965-03-17 | British Petroleum Co | Synthetic lubricants |
US3415891A (en) * | 1964-02-07 | 1968-12-10 | Takeda Chemical Industries Ltd | Stabilization of polyoxyalkylene polyols with ascorbic acid type stabilizer |
GB1162818A (en) * | 1965-12-17 | 1969-08-27 | British Petroleum Co | Synthetic Lubricants |
US3879308A (en) * | 1973-05-14 | 1975-04-22 | Lubrizol Corp | Lubricants and fuels containing ester-containing compositions |
US4302349A (en) * | 1979-06-26 | 1981-11-24 | Chemische Werke Huls, A.G. | Adducts of alcohols and olefin oxides, suitable for reducing the interfacial surface tension of oily phases with respect to water |
US4302343A (en) * | 1979-04-02 | 1981-11-24 | The Dow Chemical Company | Rotary screw compressor lubricants |
US4362635A (en) * | 1978-10-05 | 1982-12-07 | Bayer Aktiengesellschaft | Lactone-modified ester oils |
US4370247A (en) * | 1980-07-29 | 1983-01-25 | Exxon Research And Engineering Co. | Gear and axle oil composition |
US4409187A (en) * | 1980-03-22 | 1983-10-11 | Bayer Aktiengesellschaft | Sealing agent and lubricant for medium-pressure and high-pressure autoclaves |
US4430490A (en) * | 1982-08-10 | 1984-02-07 | Ppg Industries, Inc. | Polyether polyols and their method of preparation |
US4476038A (en) * | 1982-01-20 | 1984-10-09 | Th. Goldschmidt Ag | Composition for preventing or eliminating foam, especially in aqueous systems |
US4496632A (en) * | 1982-12-16 | 1985-01-29 | Basf Wyandotte Corporation | Process for lubricating synthetic fibers |
US4501616A (en) * | 1979-06-26 | 1985-02-26 | Th. Goldschmidt Ag | Lubricant and mold-release agent for the manufacture of ties |
-
1986
- 1986-12-23 JP JP61305546A patent/JPS62187799A/en active Pending
-
1989
- 1989-06-22 US US07/370,356 patent/USRE33658E/en not_active Expired - Lifetime
Patent Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB933721A (en) * | 1960-02-15 | 1963-08-14 | British Petroleum Co | Synthetic lubricants |
GB986066A (en) * | 1962-10-02 | 1965-03-17 | British Petroleum Co | Synthetic lubricants |
US3415891A (en) * | 1964-02-07 | 1968-12-10 | Takeda Chemical Industries Ltd | Stabilization of polyoxyalkylene polyols with ascorbic acid type stabilizer |
GB1162818A (en) * | 1965-12-17 | 1969-08-27 | British Petroleum Co | Synthetic Lubricants |
US3879308A (en) * | 1973-05-14 | 1975-04-22 | Lubrizol Corp | Lubricants and fuels containing ester-containing compositions |
US4362635A (en) * | 1978-10-05 | 1982-12-07 | Bayer Aktiengesellschaft | Lactone-modified ester oils |
US4302343A (en) * | 1979-04-02 | 1981-11-24 | The Dow Chemical Company | Rotary screw compressor lubricants |
US4302349A (en) * | 1979-06-26 | 1981-11-24 | Chemische Werke Huls, A.G. | Adducts of alcohols and olefin oxides, suitable for reducing the interfacial surface tension of oily phases with respect to water |
US4501616A (en) * | 1979-06-26 | 1985-02-26 | Th. Goldschmidt Ag | Lubricant and mold-release agent for the manufacture of ties |
US4409187A (en) * | 1980-03-22 | 1983-10-11 | Bayer Aktiengesellschaft | Sealing agent and lubricant for medium-pressure and high-pressure autoclaves |
US4370247A (en) * | 1980-07-29 | 1983-01-25 | Exxon Research And Engineering Co. | Gear and axle oil composition |
US4476038A (en) * | 1982-01-20 | 1984-10-09 | Th. Goldschmidt Ag | Composition for preventing or eliminating foam, especially in aqueous systems |
US4430490A (en) * | 1982-08-10 | 1984-02-07 | Ppg Industries, Inc. | Polyether polyols and their method of preparation |
US4496632A (en) * | 1982-12-16 | 1985-01-29 | Basf Wyandotte Corporation | Process for lubricating synthetic fibers |
Non-Patent Citations (1)
Title |
---|
Carswell, et al, "A Blend of a Polyglycol and a Tetra Ester as a Lubricant for Rotary Screw Air Compressors", Lubrication Engineering, vol. 39, 11, 684-689. |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5225094A (en) * | 1991-12-18 | 1993-07-06 | Exxon Research And Engineering Company | Lubricating oil having an average ring number of less than 1.5 per mole containing a succinic anhydride amine rust inhibitor |
US6841522B2 (en) * | 1998-10-28 | 2005-01-11 | Imperial Chemical Industries Plc | Lubricant compositions |
CN111040848A (en) * | 2019-12-17 | 2020-04-21 | 魏平 | High-performance air compressor oil and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JPS62187799A (en) | 1987-08-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4751012A (en) | Lubricants for reciprocating air compressors | |
US4302343A (en) | Rotary screw compressor lubricants | |
AU755427B2 (en) | Poly(neopentyl polyol) ester based coolants and improved additive package | |
US6127324A (en) | Lubricating composition containing a blend of a polyalkylene glycol and an alkyl aromatic and process of lubricating | |
AU2003265939B2 (en) | Biodegradable vegetable oil compositions | |
EP0647701B1 (en) | Refrigerator lubricant and refrigerant composition containing the same | |
EP0378176B1 (en) | Lubricants for refrigeration compressors | |
EP2271732B1 (en) | Polyalkylene glycol lubricant composition | |
US3218256A (en) | Lubricating compositions | |
US5620950A (en) | Lubricated refrigerant composition containing alicyclic epoxy compounds | |
USRE33658E (en) | Lubricants for reciprocating air compressors | |
EP0017072B1 (en) | Water-resistant lubricant for compressors and marine engines | |
JPH07228882A (en) | Gas turbine oil composition | |
EP0796908A1 (en) | Oxidation resistant lubricant | |
CA2403540A1 (en) | Synergystic combination of aryl amine antioxidants in aviation turbine oils | |
JP3005280B2 (en) | Lubricating oil composition | |
WO2001064820A1 (en) | Lubricating composition containing a blend of a polyalkylene glycol and an alkyl aromatic and process of lubricating |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FPAY | Fee payment |
Year of fee payment: 4 |
|
FPAY | Fee payment |
Year of fee payment: 8 |
|
FPAY | Fee payment |
Year of fee payment: 12 |