EP0781316A4 - Enhanced hydrocarbon lubricants for use with immiscible refrigerants - Google Patents

Enhanced hydrocarbon lubricants for use with immiscible refrigerants

Info

Publication number
EP0781316A4
EP0781316A4 EP95931605A EP95931605A EP0781316A4 EP 0781316 A4 EP0781316 A4 EP 0781316A4 EP 95931605 A EP95931605 A EP 95931605A EP 95931605 A EP95931605 A EP 95931605A EP 0781316 A4 EP0781316 A4 EP 0781316A4
Authority
EP
European Patent Office
Prior art keywords
composition
lubricant
refrigerant
oil
hydrocarbon
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.)
Withdrawn
Application number
EP95931605A
Other languages
German (de)
French (fr)
Other versions
EP0781316A1 (en
Inventor
Jose L Reyes-Gavilan
Alan D Eckard
Thomas G Flak
Todd R Tritcak
Leonard Aconsky
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.)
Witco Corp
Original Assignee
Witco Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US08/301,694 external-priority patent/US5792383A/en
Application filed by Witco Corp filed Critical Witco Corp
Publication of EP0781316A1 publication Critical patent/EP0781316A1/en
Publication of EP0781316A4 publication Critical patent/EP0781316A4/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/02Materials undergoing a change of physical state when used
    • C09K5/04Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
    • C09K5/041Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
    • C09K5/044Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
    • C09K5/045Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds containing only fluorine as halogen
    • 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
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • 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
    • C10M101/00Lubricating compositions characterised by the base-material being a mineral or fatty oil
    • C10M101/02Petroleum fractions
    • 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
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/02Well-defined hydrocarbons
    • C10M105/06Well-defined hydrocarbons aromatic
    • 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
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/38Esters 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
    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/02Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
    • 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
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/04Hydroxy compounds
    • C10M129/06Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M129/08Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least 2 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
    • C10M131/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing halogen
    • C10M131/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing halogen containing carbon, hydrogen and halogen 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
    • C10M131/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing halogen
    • C10M131/08Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing halogen containing carbon, hydrogen, halogen and oxygen
    • C10M131/10Alcohols; Ethers; Aldehydes; Ketones
    • 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
    • C10M131/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing halogen
    • C10M131/08Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing halogen containing carbon, hydrogen, halogen and oxygen
    • C10M131/12Acids; Salts or esters 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
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
    • 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
    • C10M171/00Lubricating 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
    • C10M171/008Lubricant compositions compatible with refrigerants
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2205/00Aspects relating to compounds used in compression type refrigeration systems
    • C09K2205/24Only one single fluoro component present
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/06Well-defined aromatic 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/06Well-defined aromatic compounds
    • C10M2203/065Well-defined aromatic compounds used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/1006Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/102Aliphatic fractions
    • C10M2203/1025Aliphatic fractions used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/104Aromatic fractions
    • C10M2203/1045Aromatic fractions used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/106Naphthenic fractions
    • C10M2203/1065Naphthenic fractions used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/108Residual fractions, e.g. bright stocks
    • C10M2203/1085Residual fractions, e.g. bright stocks used as base material
    • 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
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • 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
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/0206Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers used as base material
    • 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/122Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • 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
    • C10M2207/283Esters of polyhydroxy compounds
    • C10M2207/2835Esters of polyhydroxy compounds used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/286Esters of polymerised unsaturated acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/30Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/02Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
    • C10M2211/022Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
    • 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
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/04Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
    • C10M2211/044Acids; Salts or esters 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
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated 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
    • C10M2219/046Overbasedsulfonic acid 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
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/085Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing carboxyl groups; 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
    • 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
    • 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
    • C10M2223/042Metal 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
    • 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
    • C10M2223/043Ammonium or amine salts thereof

Definitions

  • This application is a continuation-in-part of application Serial No. 08/426,500 filed April 20, 1995 and application Serial No. 08/301,694 filed September 7, 1994.
  • This invention relates to fluid refrigeration compositions comprising a hydrocarbon lubricant, such as mineral oil, a refrigerant immiscible with the hydrocarbon lubricant, and additive capable of reducing the interfacial tension between the hydrocarbon lubricant and the immiscible refrigerant.
  • this invention comprises a fluid refrigeration composition
  • a fluid refrigeration composition comprising a hydrocarbon lubricant, such as mineral oil, a fluorohydrocarbon refrigerant immiscible with the hydrocarbon lubricant and a surfactant capable of reducing the interfacial tension between the hydrocarbon lubricant and fluorohydrocarbon refrigerant.
  • CFCs chlorofluorocarbons
  • CFC-115 (1-chloro-l,1,2,2,2- pentafluoroethane)
  • CFC-113 1,1,2-trichloro-l,2,2- trifluoroethane
  • HCFC hydrochlorofluorocarbon
  • HFC hydrofluorocarbon
  • R-22 hydrochlorodifluoromethane
  • R-123 (1,l-dichloro-2,2,2- trifluoroethane
  • R-124 l-chloro-l,2,2,2-tetrafluoro- ethane
  • HCFCs have much lower ozone depletion potentials than do CFCs because even though there is chlorine present in these molecules, they contain hydrogen atoms that cause their decomposition to take place at lower levels of the atmosphere.
  • HFCs examples include R-134a (1,1,1,2- tetrafluoroethane) , R-152a (1,l-difluoroethane) , R-32
  • HFC refrigerants may have desirable physical properties that make them appropriate long term refrigerant alternates, they lack miscibility with naphthenic mineral oils traditionally used as refrigeration compressor lubricants.
  • the mineral oils' chemical stability and miscibility with CFC and HCFC refrigerants, chemical compatibility with all system components, low floe and pour points, high dielectric strength, and proper viscosity provide the properties that enhance their overall performance once charged into the system.
  • the use of naphthenic refrigeration oils in refrigeration or air conditioning applications where HFCs are employed as refrigerants has been considered by some to be inappropriate due to the immiscibility of both fluids.
  • immiscibility or poor dispersibility between the refrigerant and lubricant at unit operating temperatures may provide unsuitable oil return to the compressor. This causes improper heat transfer due to oil coating of the inner surface of the heat exchange coils, and in extreme cases, lubricant starvation of the compressor.
  • the former causes energy efficiency losses, and the latter results in unit burn ⁇ out.
  • Reyes-Gavilan has shown that by using low viscosity naphthenic mineral oil (70 SUS at 37.8 ⁇ C) in the same type of units as those tested by Sanvordenker, the dependence of oil return on unit configuration is eradicated.
  • the agents responsible for oil return in household refrigeration systems aside from low viscosity mineral oils with good flow characteristics in the system and proper lubrication performance in the compressors, are high refrigerant velocities and short return lines between the evaporator and compressor. It is conceivable that those refrigeration or air conditioning systems with either low refrigerant velocities and/or long return lines between the evaporator and the compressor can experience poor oil return, resulting in any of the aforementioned system performance problems.
  • U.S. Patent No. 5,114,605 to Mitsui Petrochemical discloses a composition comprising a hydrofluorocarbon, polyether carbonate and either a mineral oil or alpha olefin oligomer.
  • the general object of this invention is to provide refrigeration fluid compositions comprising a hydrocarbon lubricant, preferably a mineral oil lubricant, and a refrigerant immiscible with the hydrocarbon lubricant containing at least one carbon and one fluorine atom.
  • a more specific object of this invention is to provide refrigeration fluid compositions comprising a mineral oil lubricant and a hydrofluorocarbon refrigerant immiscible with mineral oil.
  • refrigeration fluid compositions comprising a hydrocarbon lubricant, a refrigerant immiscible with the hydrocarbon lubricant containing at least one carbon atom and one fluorine atom, and an effective amount of an additive capable of reducing the interfacial tension between the hydrocarbon lubricant and the immiscible refrigerant.
  • composition of this invention can be used in refrigeration and air conditioning systems with potential oil return difficulties, when charged with straight hydrocarbon oil and HFC refrigerants.
  • the aim is to facilitate oil return to the compressor by making the refrigerant and hydrocarbon lubricant more dispersible with each other, allowing the refrigerant to wash the lubricant off the inner surfaces of the heat exchangers.
  • the invention provides proper lubrication and energy efficiency to the unit, while maintaining adequate chemical and thermal stability within the system.
  • the refrigeration fluid compositions of this invention comprise a hydrocarbon lubricating oil, a refrigerant containing at least one carbon and one fluorine atom and an additive capable of reducing the interfacial tension between the hydrocarbon lubricant and the refrigerant.
  • Suitable hydrocarbon lubricants useful in this invention include paraffinic mineral oils, naphthenic mineral oils, alkylbenzene oils, polyalphaolefins and their oligomers, and mixtures thereof. Minor amounts (1 to 20% by wt.) alkylbenzene with major amounts (99 to 80% by wt.) naphthenic mineral oil are particularly useful for improving the solubility or dispersibility of some additives (i.e. surfactants such as 2,4,7,9-tetramethyl-5- decyne-4,7-diol) in the hydrocarbon oil.
  • Suitable refrigerants useful in this invention include those which contain at least one carbon atom and one fluorine atom.
  • refrigerants examples include R-22 (chlorodifluoromethane) , R-124 (1-chloro- 1,2 , 2,2-tetrafluoroethane) , R-134a (1,1,1,2- tetrafluoroethane) , R-143a (1,l,1-trifluoroethane) , R-152a (1,1-difluoroethane) , R-32 (difluoromethane) , R-125 (1,1,1,2,2-pentafluoroethane) , and mixtures thereof such as R-404a [R-125 (44 wt. %) , R-143a (52 Wt.
  • mixtures can also contain propane as a component of the blend in those applications where the heat exchange fluid is going to be used as an interim retrofit fluid for existing refrigeration and air conditioning equipment.
  • suitable refrigerants can be used with CFC refrigerants, particularly, where residual amounts of these refrigerants are present in a system being retrofitted.
  • the additives useful in this invention for reducing the interfacial tension between lubricant and refrigerant have the property of facilitating the displacement of oil from metal surfaces by the refrigerant. This property can be determined by sealing a refrigerant immiscible at room temperature, such as R134a, with the hydrocarbon lubricant, the hydrocarbon lubricant and additive agents in a glass tube containing a steel or iron chip. A two phase system forms with the lubricating oil constituting the top layer and the refrigerant the bottom layer. The metal chip is then raised up to the oil level in the tube using a magnet and the oil is allowed to completely wet the metal surface by moving the metal chip rapidly up and down in the oil.
  • the additive is suitable for use in this invention, if the refrigerant displaces the oil when the chip is slowly lowered into the liquid refrigerant layer.
  • Suitable additives include surfactants, such as 2,4,7,9-tetramethyl-5-decyne-4,7-diol sold as Surfynol SE, fluorocarbon esters sold as FC-430, anionic fluorohydrocarbon phosphites, phosphates, carboxylates (salts and acids), sulfonates, etc. such as F(CF 2 CF 2 ) 3t08 ⁇ CH j -CH j SCH j CH j CO j Li sold as Zonyl FSA, mixture of o n
  • hydrocarbon lubricants made up of two or more components.
  • minor amounts of alkylbenzene hydrocarbons improve the solubility or dispersibility of some additives in mineral oil. While applicants do not wish to be bound by any theory, applicants believe that the interfacial tension at the refrigerant (liquid) /1GS interface is reduced to the point where the spreading coefficient (S) refrigerant liquid on steel is slightly positive or very close to zero which enables the refrigerant to displace the oil with slight agitation or due to the difference in specific gravity.
  • S is the spreading coefficient of fluid (1) against fluid (2) on the surface of a third phase, (3) a solid.
  • Y the respective interfacial tensions.
  • the additive or surface active agent can be used in the range of 0.001 to 5 parts by weight per 100 parts by weight lubricating oil. Concentrates can be prepared containing up to 100 parts by weight surface active agent per 100 parts by weight lubricating oil for purposes of adding same to refrigerating systems containing hydrocarbon lubricating oils containing no surface active agent or insufficient amounts for the desired purpose.
  • the weight ratio of lubricating oil to immiscible refrigerant can range from 0.10 to 15 parts by weight per 100 parts by weight refrigerant as is conventional in this art.
  • the weight ratio of polyol ester to hydrocarbon lubricant can range from about 1:99 to 1:3, preferably 1:19 to 1:4. Accordingly, we believe it is advantageous to retrofit hydrocarbon lubricant CFC systems to employ HFCs by adding concentrate compositions containing polyol ester and surfactant such as 2,4,7,9-tetramethyl-5-decyne-4,7- diol or fluorinated ester directly to the compressor system with or without additional hydrocarbon lubricant provided the surface active agent in the compressor system constitutes at least 0.001 parts by weight per 100 parts by weight of the lubricating fluids in the compressor.
  • the polyol ester/surfactant concentrate can comprise from about .1 to 100 parts by weight surfactant per 100 parts by weight polyol ester.
  • Suitable polyol esters comprise polyhydric alcohol esters of aliphatic monocarboxylic acids containing 4 to 25 carbon atoms alone or together with di or tricarboxylic acids.
  • Suitable polyhydric alcohols can contain from 2 to 6 hydroxy groups, such as neopentyl alcohol, 1,1,1-trimethylol ethane, 1,1,1-trimethylol propane, pentaerythritol, etc.
  • Suitable aliphatic carboxylic acids include branched and unbranched acids such as butyric acid, isobutyric acid, 2-ethylhexanoic acid, n-octanoic acid, valeric acid, isopentanoic acid, hexanoic acid, heptanoic acid, nonanoic acid, stearic acid, etc.
  • Dicarboxylic acids such as maleic acid, succinic acid, adipic acid etc. and tricarboxylic acids such as trimellitic acid can be used in small amounts to adjust the viscosity of the polyol ester.
  • Table I presents suitable stability and wear enhancing additives that may be used with hydrocarbon lubricants employing surface active agents in refrigeration and air conditioning applications with lubricant immiscible refrigerants.
  • Example I A 9 mL glass tube was charged with 0.050 mL of 70 SUS naphthenic mineral oil (Suniso IGS) containing 0.5% by weight candidate surfactant, a 6mm steel chip and 0.70 ml 1,1,1,2-tetrafluoroethane (R-134a) and sealed. A two phase system was formed with the naphthenic mineral oil constituting the top layer and the hydrofluorocarbon the bottom layer. The metal chip was completely wetted with oil by moving the chip rapidly up and down in the oil phase using a magnet. The chip was then slowly lowered into the tetrafluoroethane layer. The results are set forth below in Table II. TABLE II
  • PIB Diisoamyl
  • Tetra is (2-ethylhexanol) Oil clings to chip and glass. Pentaerytnritol
  • FC-430 Oil removed from chip and glass by R-134a Two layers very dispersible.
  • Example II A 9 ml glass tube was charged with 0.050 ml of 70 SUS naphthenic mineral oil (Suniso IGS) containing
  • Example III A multizone pump down solenoid medium temperature supermarket freezer rack in New England, equipped with two five door freezer rack cabinets (each 105.6 ft 3 ), a compressor (Copelametic Model No. R-76 WMT3T) located approximately 6 to 7 ft. off the ground, and evaporators on the floor of each cabinet was retrofitted. The refrigerant gas and oil travel through approximately 20 ft. of 7/8 inch diameter vertical and horizontal suction return lines before arriving at the compressor through a 1 3/8 inch tube. The system was charged with R-402A (30 pound charge) , which comprised 38 wt. % R125 (pentafluoroethane) , 60 wt.
  • R-402A (30 pound charge) , which comprised 38 wt. % R125 (pentafluoroethane) , 60 wt.
  • the oil was drained from the system leaving some residual alkylbenzene; charged with 150 SUS oil comprising primarily naphthenic mineral oil, 10 wt. % alkylbenzene, and 0.05 wt. % Surfynol SE; evacuated for 1/2 hour and allowed to run for 1 hour to flush residual alkylbenzene oil from the system. During this time, the oil pressure switch did not go off and -17°F and -10°F temperature were attained for the respective racks. After 1 hour, the oil was drained again from the system and replaced with fresh 150 SUS oil comprising primarily naphthenic mineral oil, 10 wt. % alkylbenzene, and 0.05 wt. % Surfynol SE.
  • Example IV The compositions listed below in Table III have been tested with R-134a and 2,4,7,9-tetramethyl-5-decyne- 4,7-diol surfactants with encouraging results.
  • H-l stands for a 12cSt naphthenic mineral oil at 40°C
  • H-2 stands for a 38cSt white naphthenic mineral oil at 40°C
  • H-3 stands for a 29 to 30cSt naphthenic mineral oil at 40°C
  • H-4 stands for an 18cSt naphthenic mineral oil at 40°C
  • H-5 stands for 29 to 30cSt alkylbenzene at 40°C
  • PI stands for a polyester of tri ethylol propane, 70% valeric acid and 30% isovaleric acid
  • P2 stands for a polyester of pentaerythritol and 2-ethylhexanoic acid
  • P3 stands for a polyester of pentaerythritol, valeric acid, isovaleric acid and adipic acid.
  • Example v This example illustrates that anionic fluorohydrocarbons surfactants can be used in this invention.
  • Example II was repeated using an ISO 10 naphthenic mineral oil and the candidate anionic and nonionic fluorohydrocarbon surface active agents listed below in Table IV.
  • Zonyl FSN and Zonyl FSO are F(CF 2 CF 2 ) 3 _ 8 -CH 2 CH 2 0(CH 2 CH 2 0) x H having different levels of oxyethylene units.
  • Table AN stands for anionic and NON stands for nonionic.
  • lubricant compositions comprising mixtures of either 90% by weight mineral oil and 10% by weight polyester or 70% by weight mineral oil and 30% by weight polyester were tested in the manner described in Example II using ISO 10 naphthenic mineral oil and either polyester P-l, which stands for a polyolester of trimethylol propane and 30% valeric acid and P-2, which stands for a polyolester of 2-ethylhexanoic acid, 79% neopentyl glycol and 21% pentaerythritol.
  • polyester P-l which stands for a polyolester of trimethylol propane and 30% valeric acid
  • P-2 which stands for a polyolester of 2-ethylhexanoic acid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Thermal Sciences (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Lubricants (AREA)

Abstract

Fluid refrigeration compositions comprising a hydrocarbon lubricant, an immiscible refrigerant and an additive capable of reducing the interfacial tension between the hydrocarbon lubricant and refrigerant.

Description

ENHANCED HYDROCARBON LUBRICANTS FOR USE WITH IMMISCIBLE REFRIGERANTS
This application is a continuation-in-part of application Serial No. 08/426,500 filed April 20, 1995 and application Serial No. 08/301,694 filed September 7, 1994. This invention relates to fluid refrigeration compositions comprising a hydrocarbon lubricant, such as mineral oil, a refrigerant immiscible with the hydrocarbon lubricant, and additive capable of reducing the interfacial tension between the hydrocarbon lubricant and the immiscible refrigerant. More particularly this invention comprises a fluid refrigeration composition comprising a hydrocarbon lubricant, such as mineral oil, a fluorohydrocarbon refrigerant immiscible with the hydrocarbon lubricant and a surfactant capable of reducing the interfacial tension between the hydrocarbon lubricant and fluorohydrocarbon refrigerant.
For approximately the past 60 years, chlorofluorocarbons (CFCs) have been commercially used as heat exchange fluids in systems designed for refrigeration and air conditioning applications. These types of compounds have also been employed as propellants, foam blowing agents, and cleaning solvents for the electronics and aerospace industries. CFC-12
(dichlorodifluoromethane) , CFC-115 (1-chloro-l,1,2,2,2- pentafluoroethane) , and CFC-113 (1,1,2-trichloro-l,2,2- trifluoroethane) are examples of such compounds.
Rowland and Molina hypothesized in the early 1970,s that the high stability inherent in CFCs provided these molecules with a very long life in the lower at osphere. Consequently, they slowly travel to the stratosphere, where chlorine radicals are removed from the CFC molecules by the effect of ultraviolet radiation from the sun. The radicals then attack the ozone found in this atmospheric layer decreasing its concentration. This prompted the aerosol industry in the mid-1970,s to gradually replace these chemicals with environmentally safer alternates that met their product specifications. In the mid-1980's, the detection of a drop in ozone concentration over Antarctica, an effect that is presently spreading to other areas of the globe, has prompted many nations to restrict and eventually ban the production and use of CFCs before the end of the century. Consequently, several compounds have been suggested for use as alternate refrigerants. These compounds belong to the hydrochlorofluorocarbon (HCFC) and hydrofluorocarbon (HFC) chemical families. Examples of HCFCs are R-22 (hydrochlorodifluoromethane) , R-123 (1,l-dichloro-2,2,2- trifluoroethane) , and R-124 (l-chloro-l,2,2,2-tetrafluoro- ethane) . HCFCs have much lower ozone depletion potentials than do CFCs because even though there is chlorine present in these molecules, they contain hydrogen atoms that cause their decomposition to take place at lower levels of the atmosphere. However, since the depletion of the ozone layer is currently continuing and expanding to other areas of the globe, there is much legislative pressure to eventually restrict and ban these chemicals as well. Hence, these are perceived as short-term refrigerant alternates. Presently used naphthenic mineral oil, alkylbenzenes, and naphthenic mineral oil/alkylbenzene blends have traditionally met the lubricating and performance needs of refrigeration systems charged with HCFCs.
Examples of HFCs are R-134a (1,1,1,2- tetrafluoroethane) , R-152a (1,l-difluoroethane) , R-32
(difluoromethane) , R-143a (1,l,l-trifluorethane) , R-125 (1,1,1,2,2-pentafluoroethane) , and azeotropic and zeotropic blends consisting of any one of these, or other, HFC components. These molecules are not ozone depleters and hence, have presently been adopted as long term alternate refrigerants. While HFC refrigerants may have desirable physical properties that make them appropriate long term refrigerant alternates, they lack miscibility with naphthenic mineral oils traditionally used as refrigeration compressor lubricants. The mineral oils' chemical stability and miscibility with CFC and HCFC refrigerants, chemical compatibility with all system components, low floe and pour points, high dielectric strength, and proper viscosity provide the properties that enhance their overall performance once charged into the system. The use of naphthenic refrigeration oils in refrigeration or air conditioning applications where HFCs are employed as refrigerants has been considered by some to be inappropriate due to the immiscibility of both fluids. The belief is that, immiscibility or poor dispersibility between the refrigerant and lubricant at unit operating temperatures may provide unsuitable oil return to the compressor. This causes improper heat transfer due to oil coating of the inner surface of the heat exchange coils, and in extreme cases, lubricant starvation of the compressor. The former causes energy efficiency losses, and the latter results in unit burn¬ out.
Jolly, et al., U.S. Patent No. 4,941,986 states that the mixture of the refrigerant and lubricant must be miscible/soluble and chemically and thermally stable over a wide temperature range, covering the operating temperature range of refrigeration and air conditioning systems. It is generally desirable for the lubricants to be miscible/soluble in the refrigerant at concentrations of about 5 to 15% over a temperature range of -40βC to 80°C. This temperature range brackets the operating temperature of many refrigeration and air conditioning system designs in the market today.
The patentees then disclose replacing the hydrocarbon lubricating oil with various synthetic materials that are much more expensive than the hydrocarbon oils. Obviously, it is economically and environmentally desirable to provide hydrocarbon oil/alternate refrigerant fluids, even though immiscible, for use in these systems. In American Society of Heating, Refrigerating and Air Conditioning Engineers, Sanvordenker (1989) and Reyes-Gavilan (1993) have independently pointed out that proper oil return is present in household refrigeration systems charged with HFC-134a and straight hydrocarbon oils. Sanvordenker has further explained that this condition is dependent on unit configuration; top-mount units with a horizontal evaporator work well, while side- by-side units with a vertical evaporator function, but not as well. Reyes-Gavilan has shown that by using low viscosity naphthenic mineral oil (70 SUS at 37.8βC) in the same type of units as those tested by Sanvordenker, the dependence of oil return on unit configuration is eradicated. The agents responsible for oil return in household refrigeration systems, aside from low viscosity mineral oils with good flow characteristics in the system and proper lubrication performance in the compressors, are high refrigerant velocities and short return lines between the evaporator and compressor. It is conceivable that those refrigeration or air conditioning systems with either low refrigerant velocities and/or long return lines between the evaporator and the compressor can experience poor oil return, resulting in any of the aforementioned system performance problems.
Prior art teaching the use of hydrocarbon oils in refrigeration or air conditioning systems employing HFC refrigerants is limited. U.S. Patent No. 5,096,606 to Kao Corporation, discloses and claims compositions comprising HFCs and polyol esters, which can be blended with other lubricants.
U.S. Patent No. 5,114,605 to Mitsui Petrochemical discloses a composition comprising a hydrofluorocarbon, polyether carbonate and either a mineral oil or alpha olefin oligomer.
Abstract of Japanese Patent No. 4,018,491 discloses that blends of an ester oil and a hydrocarbon oil such as mineral oil are compatible with hydrofluorocarbon refrigerants wherein the ratio of ester oil to hydrocarbon oil is at least unity.
Abstract of Japanese Patent No. 1,115,998 discloses blends of an alkylbenzene, a mineral oil and a hydrofluorocarbon refrigerant. Lubrizol PCT WO/12849 suggests using viscosity adjusters such as naphthenic mineral oils. However, no mention is made of improvement in dispersibility or miscibility/solubility characteristics of the hydrocarbon lubricant in the presence of HFC refrigerants. These references teach those skilled in the art the possibility of using blends comprising hydrocarbon lubricants in HFC refrigeration and air conditioning applications. The industry has noted however; that many hydrocarbon lubricant CFC systems retrofitted to employ HFC/polyol ester fluids have shown performance degradations, indicative of poor oil return to the compressor, when the residual mineral oil content in the polyol ester exceeds 1% of the total lubricant in the system. For purposes of this invention, the term
"immiscible" means that a two-phase system is formed between refrigerant and lubricant, at least at any point in the typical operating range of -40°C to 80βC in the refrigeration or air conditioning systems. The general object of this invention is to provide refrigeration fluid compositions comprising a hydrocarbon lubricant, preferably a mineral oil lubricant, and a refrigerant immiscible with the hydrocarbon lubricant containing at least one carbon and one fluorine atom. A more specific object of this invention is to provide refrigeration fluid compositions comprising a mineral oil lubricant and a hydrofluorocarbon refrigerant immiscible with mineral oil. Other objects appear hereinafter.
We have now found that the objects of this invention can be obtained with refrigeration fluid compositions comprising a hydrocarbon lubricant, a refrigerant immiscible with the hydrocarbon lubricant containing at least one carbon atom and one fluorine atom, and an effective amount of an additive capable of reducing the interfacial tension between the hydrocarbon lubricant and the immiscible refrigerant.
The composition of this invention can be used in refrigeration and air conditioning systems with potential oil return difficulties, when charged with straight hydrocarbon oil and HFC refrigerants. The aim is to facilitate oil return to the compressor by making the refrigerant and hydrocarbon lubricant more dispersible with each other, allowing the refrigerant to wash the lubricant off the inner surfaces of the heat exchangers. The invention provides proper lubrication and energy efficiency to the unit, while maintaining adequate chemical and thermal stability within the system.
Briefly, the refrigeration fluid compositions of this invention comprise a hydrocarbon lubricating oil, a refrigerant containing at least one carbon and one fluorine atom and an additive capable of reducing the interfacial tension between the hydrocarbon lubricant and the refrigerant.
Suitable hydrocarbon lubricants useful in this invention include paraffinic mineral oils, naphthenic mineral oils, alkylbenzene oils, polyalphaolefins and their oligomers, and mixtures thereof. Minor amounts (1 to 20% by wt.) alkylbenzene with major amounts (99 to 80% by wt.) naphthenic mineral oil are particularly useful for improving the solubility or dispersibility of some additives (i.e. surfactants such as 2,4,7,9-tetramethyl-5- decyne-4,7-diol) in the hydrocarbon oil. Suitable refrigerants useful in this invention include those which contain at least one carbon atom and one fluorine atom. Examples of suitable refrigerants include R-22 (chlorodifluoromethane) , R-124 (1-chloro- 1,2 , 2,2-tetrafluoroethane) , R-134a (1,1,1,2- tetrafluoroethane) , R-143a (1,l,1-trifluoroethane) , R-152a (1,1-difluoroethane) , R-32 (difluoromethane) , R-125 (1,1,1,2,2-pentafluoroethane) , and mixtures thereof such as R-404a [R-125 (44 wt. %) , R-143a (52 Wt. %) , R-134a (4.0 wt. %) ] . These mixtures can also contain propane as a component of the blend in those applications where the heat exchange fluid is going to be used as an interim retrofit fluid for existing refrigeration and air conditioning equipment. If desired, the suitable refrigerants can be used with CFC refrigerants, particularly, where residual amounts of these refrigerants are present in a system being retrofitted.
The additives useful in this invention for reducing the interfacial tension between lubricant and refrigerant have the property of facilitating the displacement of oil from metal surfaces by the refrigerant. This property can be determined by sealing a refrigerant immiscible at room temperature, such as R134a, with the hydrocarbon lubricant, the hydrocarbon lubricant and additive agents in a glass tube containing a steel or iron chip. A two phase system forms with the lubricating oil constituting the top layer and the refrigerant the bottom layer. The metal chip is then raised up to the oil level in the tube using a magnet and the oil is allowed to completely wet the metal surface by moving the metal chip rapidly up and down in the oil. The additive is suitable for use in this invention, if the refrigerant displaces the oil when the chip is slowly lowered into the liquid refrigerant layer.
Suitable additives include surfactants, such as 2,4,7,9-tetramethyl-5-decyne-4,7-diol sold as Surfynol SE, fluorocarbon esters sold as FC-430, anionic fluorohydrocarbon phosphites, phosphates, carboxylates (salts and acids), sulfonates, etc. such as F(CF2CF2)3t08 ~ CHj-CHjSCHjCHjCOjLi sold as Zonyl FSA, mixture of o n
F ( CF2CP2 ) 3t(jβ -CH2CH20-P (0NH4 ) 2 and [ F ( CF2CF2 ) 3t<jβ -CH2-CH20 ] 2
O u -PONH4 sold as Zonyl FSP, Zonyl FSJ, etc.
In some cases, it can be desirable to enhance the solubility of surfactants in the hydrocarbon lubricants with cosolvents or by using hydrocarbon lubricants made up of two or more components. For example, as indicated above, minor amounts of alkylbenzene hydrocarbons improve the solubility or dispersibility of some additives in mineral oil. While applicants do not wish to be bound by any theory, applicants believe that the interfacial tension at the refrigerant (liquid) /1GS interface is reduced to the point where the spreading coefficient (S) refrigerant liquid on steel is slightly positive or very close to zero which enables the refrigerant to displace the oil with slight agitation or due to the difference in specific gravity.
The concept of spreading coefficient is defined by: Y = gamma.
S = Y 23 " Y12 " Y13
Where S is the spreading coefficient of fluid (1) against fluid (2) on the surface of a third phase, (3) a solid. The "Y" terms are the respective interfacial tensions.
Spontaneous spreading will occur if S>0. Other influences such as differences in specific gravity or mechanical shear energy also apply, but S will denote the contribution of interfacial tensions as influenced by additives or surface active agents. 1 = refrigerant
2 = 1GS
3 = Steel Surface in the case where no additive is present
0 > Y23 - Y12 - Y13 and Y12 is a significant positive number as is apparent from the prominent meniscus between the two phases. Also, since the oil preferentially wets and continues to wet the steel even with some degree of agitation;
Y13 > Y23 This leads to the conclusion that Y12 + Y13 > Y23
Upon the addition of certain surfactants, a different behavior results which is described by: o < γ23 - γ12 - γ13 by observation: Y12 → 0 (flat meniscus) γ 23 ≥ γi3 (refrigerant displaces oil on steel surface)
This leads to the conclusion that the spreading coefficient for refrigerant on steel approaches 0 or becomes slightly positive, in the presence of certain additives which reduce Y12 + Y13 faster than Y23.
The additive or surface active agent can be used in the range of 0.001 to 5 parts by weight per 100 parts by weight lubricating oil. Concentrates can be prepared containing up to 100 parts by weight surface active agent per 100 parts by weight lubricating oil for purposes of adding same to refrigerating systems containing hydrocarbon lubricating oils containing no surface active agent or insufficient amounts for the desired purpose. The weight ratio of lubricating oil to immiscible refrigerant can range from 0.10 to 15 parts by weight per 100 parts by weight refrigerant as is conventional in this art. As indicated above, the industry has noted that many hydrocarbon lubricant/CFC systems retrofitted to employ HFC/polyol ester fluids have shown performance degradations, indicative of poor oil return to the compressor, when the residual mineral oil content in the polyol ester exceeds 1% of the total lubricant in the system. Surprisingly, we have found that the addition of relatively small amounts of polyol ester lubricants to the compositions of this invention improves the solubility or dispersibility of some additives (i.e. surfactants such as 2,4,7,9-tetramethyl-5-decyne-4,7-diol) in the hydrocarbon oil. In such case the weight ratio of polyol ester to hydrocarbon lubricant can range from about 1:99 to 1:3, preferably 1:19 to 1:4. Accordingly, we believe it is advantageous to retrofit hydrocarbon lubricant CFC systems to employ HFCs by adding concentrate compositions containing polyol ester and surfactant such as 2,4,7,9-tetramethyl-5-decyne-4,7- diol or fluorinated ester directly to the compressor system with or without additional hydrocarbon lubricant provided the surface active agent in the compressor system constitutes at least 0.001 parts by weight per 100 parts by weight of the lubricating fluids in the compressor. The polyol ester/surfactant concentrate can comprise from about .1 to 100 parts by weight surfactant per 100 parts by weight polyol ester.
Suitable polyol esters comprise polyhydric alcohol esters of aliphatic monocarboxylic acids containing 4 to 25 carbon atoms alone or together with di or tricarboxylic acids. Suitable polyhydric alcohols can contain from 2 to 6 hydroxy groups, such as neopentyl alcohol, 1,1,1-trimethylol ethane, 1,1,1-trimethylol propane, pentaerythritol, etc. Suitable aliphatic carboxylic acids include branched and unbranched acids such as butyric acid, isobutyric acid, 2-ethylhexanoic acid, n-octanoic acid, valeric acid, isopentanoic acid, hexanoic acid, heptanoic acid, nonanoic acid, stearic acid, etc. Dicarboxylic acids, such as maleic acid, succinic acid, adipic acid etc. and tricarboxylic acids such as trimellitic acid can be used in small amounts to adjust the viscosity of the polyol ester.
Table I presents suitable stability and wear enhancing additives that may be used with hydrocarbon lubricants employing surface active agents in refrigeration and air conditioning applications with lubricant immiscible refrigerants.
TABLE I Example of Suitable Additives
(Stabilizing and Antiwear)
Trade Name Additive Chemical and Functional Wt. % Characterization
BHT Phenolic antioxidant 0.5
Irganox L-57 Amine antioxidant 0.5
Rβotnet 39 Triazole derivative copper 0.5 corrosion inhibitor
ERL 4221 Epoxide 0.5
Syn-O-Ad 8478 Triaryl phosphate ester antiwear 5.0 agent
Durad 620B Phosphate ester antiwear agent 5.0
Additive RC8210 Sulfur zed extreme pressure agent 2.5
Example I A 9 mL glass tube was charged with 0.050 mL of 70 SUS naphthenic mineral oil (Suniso IGS) containing 0.5% by weight candidate surfactant, a 6mm steel chip and 0.70 ml 1,1,1,2-tetrafluoroethane (R-134a) and sealed. A two phase system was formed with the naphthenic mineral oil constituting the top layer and the hydrofluorocarbon the bottom layer. The metal chip was completely wetted with oil by moving the chip rapidly up and down in the oil phase using a magnet. The chip was then slowly lowered into the tetrafluoroethane layer. The results are set forth below in Table II. TABLE II
Surface Active Agent Blend Behavior
Diisoamyl (PIB) Succinate Oil clings to chip. Oil clings to glass.
EXP 5159-197 (Fluorinated ester Improvement in dispersibility made by Organics) but oil clings to chip and glass.
Tetra is (2-ethylhexanol) Oil clings to chip and glass. Pentaerytnritol
Surfynol SE Oil removed from chip and glass by refrigerant. Two layers very dispersible.
Surfynol TG Oil clings to chip and glass.
EX 1038 (Carboxylic acid dimer Oil clings to chip and glass. ester)
FC-430 Oil removed from chip and glass by R-134a. Two layers very dispersible.
FC-431 Oil clings to chip and glass.
FC-740 Oil clings to chip and glass. Excessive frothing.
The above data clearly shows Surfynol SE comprising 2,4,7,9-tetramethyl-5-decyne-4,7-diol and FC- 430 comprising a fluorinated ester are suitable for use in this invention.
Example II A 9 ml glass tube was charged with 0.050 ml of 70 SUS naphthenic mineral oil (Suniso IGS) containing
0.05% by weight candidate surfactant (Surfynol SE or FC- 430), a 6mm steel chip and 0.70 ml 1,1,1,2 tetrafluoroethane (R-134a) and sealed. A two phase system was formed with the naphthenic mineral oil constituting the top layer and the hydrofluorocarbon the bottom layer. The metal chip was completely wet with oil by moving the chip rapidly up and down in the oil phase using a magnet. The chip was then slowly lowered into the tetrafluoroethane layer. For both candidates, the oil is removed from the chip and glass by the R-134a. Both lubricant and refrigerant layers are very dispersible with each other, causing the oil to be removed from the surface of the chip and glass by R-134a.
Example III A multizone pump down solenoid medium temperature supermarket freezer rack in New England, equipped with two five door freezer rack cabinets (each 105.6 ft3), a compressor (Copelametic Model No. R-76 WMT3T) located approximately 6 to 7 ft. off the ground, and evaporators on the floor of each cabinet was retrofitted. The refrigerant gas and oil travel through approximately 20 ft. of 7/8 inch diameter vertical and horizontal suction return lines before arriving at the compressor through a 1 3/8 inch tube. The system was charged with R-402A (30 pound charge) , which comprised 38 wt. % R125 (pentafluoroethane) , 60 wt. % R22 (hydrochlorodifluoromethane) , and 2 wt. % R290 (propane) and a 200 SUS alkylbenzene lubricating oil containing antiwear and foaming agents. As the unit operated below -5°F, the lubricant level in the compressor went down and the oil pressure switch turned off the unit. The system was then operated at about 0°F to maintain proper oil pressure and lubrication.
The oil was drained from the system leaving some residual alkylbenzene; charged with 150 SUS oil comprising primarily naphthenic mineral oil, 10 wt. % alkylbenzene, and 0.05 wt. % Surfynol SE; evacuated for 1/2 hour and allowed to run for 1 hour to flush residual alkylbenzene oil from the system. During this time, the oil pressure switch did not go off and -17°F and -10°F temperature were attained for the respective racks. After 1 hour, the oil was drained again from the system and replaced with fresh 150 SUS oil comprising primarily naphthenic mineral oil, 10 wt. % alkylbenzene, and 0.05 wt. % Surfynol SE. Both freezers have been operated for two months at -10°F to -15°F with no oil return difficulties. Example IV The compositions listed below in Table III have been tested with R-134a and 2,4,7,9-tetramethyl-5-decyne- 4,7-diol surfactants with encouraging results. In the Table, H-l stands for a 12cSt naphthenic mineral oil at 40°C, H-2 stands for a 38cSt white naphthenic mineral oil at 40°C, H-3 stands for a 29 to 30cSt naphthenic mineral oil at 40°C, H-4 stands for an 18cSt naphthenic mineral oil at 40°C, H-5 stands for 29 to 30cSt alkylbenzene at 40°C, PI stands for a polyester of tri ethylol propane, 70% valeric acid and 30% isovaleric acid, P2 stands for a polyester of pentaerythritol and 2-ethylhexanoic acid and P3 stands for a polyester of pentaerythritol, valeric acid, isovaleric acid and adipic acid.
TABLE III
Lubricants in Parts by Weight Surfactants in Parts by Weight
99.95 H-l .05
91.90 H-l and 8.0 P-l .10
87.80 H-l and 12.0 P-l .20
99.95 H-2 .05
84.90 H-2 and 15.0 P-2 .10
84.80 H-2 and 15.0 P-2 .20
89.95 H-3 and 10.0 H-5 .05 89.90 H-3 and 10.0 P-3 .10 84.80 H-3 and 15.0 P-3 .20
94.45 H-4 and 5.0 H-5 .05 94.40 H-4 and 5.0 P-3 ,10 92.80 H-4 and 7.0 P-3 .20
Example v This example illustrates that anionic fluorohydrocarbons surfactants can be used in this invention. Example II was repeated using an ISO 10 naphthenic mineral oil and the candidate anionic and nonionic fluorohydrocarbon surface active agents listed below in Table IV. Zonyl FSN and Zonyl FSO are F(CF2CF2)3_8 -CH2CH20(CH2CH20)xH having different levels of oxyethylene units. In the Table AN stands for anionic and NON stands for nonionic. TABLE IV
Surfactant Type Wt% Activity
Zonyl FSP AN .05 Partial removal of oil from chip. .50 Complete removal of oil from chip.
Zonyl FSA AN .05 None .50 Partial removal of oil from chip.
Zonyl FSJ AN .05 Complete removal of oil from chip. .50 Complete removal of oil from chip.
Zonyl FSN NON .05 None .50 None
Zonyl FSO NON .05 None .50 None
The above data clearly shows that anionic fluorohydrocarbons surfactants are suitable for use in this invention.
Comparison Example
In an attempt to displace lubricant from chip without using any additive of this invention lubricant compositions comprising mixtures of either 90% by weight mineral oil and 10% by weight polyester or 70% by weight mineral oil and 30% by weight polyester were tested in the manner described in Example II using ISO 10 naphthenic mineral oil and either polyester P-l, which stands for a polyolester of trimethylol propane and 30% valeric acid and P-2, which stands for a polyolester of 2-ethylhexanoic acid, 79% neopentyl glycol and 21% pentaerythritol. The results are set forth below in Table V.
TABLE V
Polyester Wt% Polyester Results
P-l 10% Oil clings to chip and glass. 30% Oil clings to chip and glass.
P-2 10% Oil clings to chip and glass. 30% Oil clings to chip and glass.

Claims

We Claim:
1. A fluid refrigeration composition comprising a hydrocarbon lubricant, a refrigerant immiscible with the hydrocarbon lubricant containing at least one carbon atom and one fluorine atom, and an additive capable of reducing the interfacial tension at the interface between the hydrocarbon lubricant and the liquid refrigerant to the point where the spreading coefficient(s) refrigerant liquid on steel is slightly positive or very close to zero enabling the refrigerant to displace hydrocarbon lubricant from steel wherein said additive is present in a concentration of 0.001 to 5 parts by weight per 100 parts by weight hydrocarbon lubricant.
2. The composition of claim 1, wherein the hydrocarbon lubricant comprises a paraffinic mineral oil.
3. The composition of claim 1, wherein the hydrocarbon lubricant comprises a naphthenic oil.
4. The composition of claim 1, wherein the hydrocarbon lubricant comprises an alkylbenzene oil.
5. The composition of claim 1, wherein the hydrocarbon lubricant comprises a polyalphaolefin and its oligomers.
6. The composition of claim 1, wherein the hydrocarbon lubricant comprises a major amount of naphthenic mineral oil and a minor amount of an alkylbenzene oil.
7. The composition of claim 6, wherein the hydrocarbon lubricant is a paraffinic mineral oil. 8. The composition of claim 1, wherein the refrigerant comprises a hydrofluorocarbon.
9. The composition of claim 8, wherein all the halogen groups of the hydrofluorocarbon are fluorine.
10. The composition of claim 9, wherein the hydrofluorocarbon comprises 1,1,1,2- tetrafluoroethane.
11. The composition of claim 9, wherein the hydrofluorocarbon comprises pentafluoroethane.
12. The composition of claim 9, wherein said composition also comprises difluoromonochloromethane.
13. The composition of claim 1, wherein the additive comprises a surfactant.
14. The composition of claim 13, wherein the surfactant comprises 2,4,7,9-tetramethyl-5-decyne-4,7-diol.
15. The composition of claim 14, wherein said composition contains a polyol ester lubricant in a weight ratio of polyol ester to hydrocarbon lubricant from about 1:99 to 1:3.
16. The composition of claim 13, wherein the surfactant comprises a fluoroester.
17. The composition of claim 13, wherein the surfactant comprises an anionic fluorohydrocarbon.
18. The composition of claim 1, wherein the refrigerant is immiscible over the whole temperature range of -40βC to 80°C with the lubricant. 19. A fluid refrigeration composition comprising a hydrocarbon lubricant comprising at least one member selected from the group consisting of paraffinic mineral oil, naphthenic mineral oil, alkylbenzene oil, and polyalphaolefin and their oligomers, a refrigerant immiscible with the hydrocarbon lubricant containing at least one carbon atom and one fluorine atom, and an effective amount of an additive capable of reducing the interfacial tension between the hydrocarbon lubricant and the liquid refrigerant such that the refrigerant can displace the lubricant from the inner surfaces of the heat exchangers and lines.
20. A composition comprising a polyol ester lubricant and 2,4,7,9-tetramethyl-5-decyne-4 ,7-diol.
21. The composition of claim 19, wherein said 2,4,7,9- tetramethyl-5-decyne-4,7-diol is present in a concentration of about 0.1 to 100 parts by weight per 100 parts by weight polyol ester.
22. A composition comprising a polyol ester lubricant and fluorinated ester.
23. A composition comprising a polyol ester lubricant and an anionic fluorohydrocarbon.
24. The method of retrofitting a compressor system which comprises the step of adding a concentrate comprising a polyol ester lubricant and 2,4,7,9-tetramethyl-5- decyne-4,7-diol to the compressor system.
EP95931605A 1994-09-07 1995-08-28 Enhanced hydrocarbon lubricants for use with immiscible refrigerants Withdrawn EP0781316A4 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US08/301,694 US5792383A (en) 1994-09-07 1994-09-07 Reduction of enterfacial tension between hydrocarbon lubricant and immiscible liquid refrigerant
US301694 1994-09-07
US42650095A 1995-04-20 1995-04-20
US426500 1995-04-20
PCT/US1995/010888 WO1996007721A1 (en) 1994-09-07 1995-08-28 Enhanced hydrocarbon lubricants for use with immiscible refrigerants

Publications (2)

Publication Number Publication Date
EP0781316A1 EP0781316A1 (en) 1997-07-02
EP0781316A4 true EP0781316A4 (en) 1999-07-14

Family

ID=26972550

Family Applications (1)

Application Number Title Priority Date Filing Date
EP95931605A Withdrawn EP0781316A4 (en) 1994-09-07 1995-08-28 Enhanced hydrocarbon lubricants for use with immiscible refrigerants

Country Status (14)

Country Link
EP (1) EP0781316A4 (en)
JP (1) JPH10505623A (en)
KR (1) KR970705626A (en)
CN (1) CN1053006C (en)
AU (1) AU692923B2 (en)
BR (1) BR9508899A (en)
CA (1) CA2199008A1 (en)
FI (1) FI970954A (en)
HU (1) HU218032B (en)
MX (1) MX9701644A (en)
NO (1) NO971040L (en)
NZ (1) NZ292709A (en)
PL (1) PL319054A1 (en)
WO (1) WO1996007721A1 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR9908205A (en) * 1998-01-16 2000-11-28 Du Pont Coolant composition, lubricant composition, process to produce refrigeration and process to produce heat
GB9901667D0 (en) * 1999-01-26 1999-03-17 Ici Plc Lubricant composition
EP1167495B1 (en) * 1999-03-05 2010-04-21 Idemitsu Kosan Co., Ltd. Refrigerating machine oil compositions
JP4316044B2 (en) * 1999-04-01 2009-08-19 出光興産株式会社 Refrigerator oil composition
JP2001181660A (en) * 1999-12-28 2001-07-03 Daikin Ind Ltd Working fluid and freezing device
US6516837B2 (en) 2000-09-27 2003-02-11 Honeywell International Inc. Method of introducing refrigerants into refrigeration systems
US6736991B1 (en) * 2003-02-12 2004-05-18 Crompton Corporation Refrigeration lubricant for hydrofluorocarbon refrigerants
US8796193B2 (en) 2003-08-01 2014-08-05 Nippon Oil Corporation Refrigerating machine oil compositions
US8506839B2 (en) * 2005-12-14 2013-08-13 E I Du Pont De Nemours And Company Absorption cycle utilizing ionic liquids and water as working fluids
US8980808B2 (en) 2011-08-03 2015-03-17 Cognis Ip Management Gmbh Lubricant compositions with improved oxidation stability and service life
KR102315318B1 (en) * 2017-01-13 2021-10-22 허니웰 인터내셔날 인코포레이티드 Refrigerant, heat transfer composition, method and system
CN111303427B (en) * 2020-05-14 2020-09-04 富海(东营)新材料科技有限公司 Industrial purification process of high-purity low-ash polysulfone resin

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62292895A (en) * 1986-06-13 1987-12-19 Nippon Oil & Fats Co Ltd Refrigerator oil
EP0556662A1 (en) * 1992-02-18 1993-08-25 Idemitsu Kosan Company Limited Lubricant for refrigerating machine employing refrigerant comprising tetrafluoroethane
JPH0617078A (en) * 1992-06-30 1994-01-25 Toshiba Corp Refrigerator oil composition and refrigerator
US5295357A (en) * 1991-10-31 1994-03-22 Idemitsu Kosan Co, Ltd. Method for lubricating compression type refrigerating system
EP0784090A1 (en) * 1995-06-01 1997-07-16 Harashima, Tomoko Mixed coolant composition

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3733850A (en) * 1970-01-16 1973-05-22 Chevron Res Refrigeration heat pump,and heat engine apparatus
US4175047A (en) * 1978-09-25 1979-11-20 Mobil Oil Corporation Synthetic ester and hydrogenated olefin oligomer lubricant and method of reducing fuel consumption therewith
US4900463A (en) * 1989-05-23 1990-02-13 Allied-Signal Inc. Refrigeration lubricant blends
JP2801703B2 (en) * 1989-09-01 1998-09-21 花王株式会社 Refrigerating machine oil
JP3012889B2 (en) * 1990-05-11 2000-02-28 東芝キヤリア株式会社 Refrigerant compressor
JP2901369B2 (en) * 1991-01-30 1999-06-07 株式会社日立製作所 Refrigerator oil composition, refrigerant compressor and refrigeration device incorporating the same
US5156768A (en) * 1991-04-05 1992-10-20 Allied-Signal Inc. Stabilized chlorine-containing refrigeration compositions
CN1075739A (en) * 1992-02-24 1993-09-01 中国科学院上海有机化学研究所 Cooling agent and lubricating oil system thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62292895A (en) * 1986-06-13 1987-12-19 Nippon Oil & Fats Co Ltd Refrigerator oil
US5295357A (en) * 1991-10-31 1994-03-22 Idemitsu Kosan Co, Ltd. Method for lubricating compression type refrigerating system
EP0556662A1 (en) * 1992-02-18 1993-08-25 Idemitsu Kosan Company Limited Lubricant for refrigerating machine employing refrigerant comprising tetrafluoroethane
JPH0617078A (en) * 1992-06-30 1994-01-25 Toshiba Corp Refrigerator oil composition and refrigerator
EP0784090A1 (en) * 1995-06-01 1997-07-16 Harashima, Tomoko Mixed coolant composition

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch Week 8805, Derwent World Patents Index; Class A97, AN 88-033105, XP002103522 *
PATENT ABSTRACTS OF JAPAN vol. 018, no. 222 (C - 1193) 21 April 1994 (1994-04-21) *
See also references of WO9607721A1 *

Also Published As

Publication number Publication date
HU218032B (en) 2000-05-28
FI970954A (en) 1997-05-06
NZ292709A (en) 1999-04-29
NO971040D0 (en) 1997-03-06
FI970954A0 (en) 1997-03-06
EP0781316A1 (en) 1997-07-02
CA2199008A1 (en) 1996-03-14
BR9508899A (en) 1997-11-25
CN1159205A (en) 1997-09-10
WO1996007721A1 (en) 1996-03-14
CN1053006C (en) 2000-05-31
AU692923B2 (en) 1998-06-18
HUT76913A (en) 1998-01-28
JPH10505623A (en) 1998-06-02
KR970705626A (en) 1997-10-09
NO971040L (en) 1997-05-06
PL319054A1 (en) 1997-07-21
MX9701644A (en) 1998-02-28
AU3496795A (en) 1996-03-27

Similar Documents

Publication Publication Date Title
US5866030A (en) Enhanced hydrocarbon lubricants for use with immiscible refrigerants
EP0479338B1 (en) Use of a lubricant for compressors using a hydrofluorocarbon refrigerant containing no chlorine.
US5792383A (en) Reduction of enterfacial tension between hydrocarbon lubricant and immiscible liquid refrigerant
CA2059423C (en) Lubricant composition for fluorinated refrigerants used in compression refrigeration systems
AU2001296349A1 (en) Hydrofluorocarbon refrigerant compositions soluble in lubricating oil
AU692923B2 (en) Enhanced hydrocarbon lubricants for use with immiscible refrigerants
RU2238964C2 (en) Refrigeration lubricating composition, refrigeration system, agent and method for inhibiting sedimentation and removal of undesired sediments
EP0536940B1 (en) Working fluids
CN111936606B (en) Refrigerator, refrigerator oil and working fluid composition for refrigerator
EP1193305A1 (en) Hydrofluorocarbon refrigerant compositions soluble in lubricating oil
EP0944688B1 (en) Refrigeration oil and working fluid composition for refrigerating machine
EP0897416B1 (en) Refrigeration oils comprising esters of hindered alcohols
MXPA97001644A (en) Improved hydrocarbon lubricants for use with inmiscib refrigerants
EP0704521B1 (en) Method for removing unwanted lubricating oil from a refrigeration system
JPH11228984A (en) Low viscosity, good fuel combustion polyol ester base cooling agent containing polyether and antioxidant with or without phosphate ester
KR20040007307A (en) A lubricant and a operating medium for refrigerating cycle apparatus in a coolant-compressed type
WO2004072215A1 (en) Lubricant for hydrofluorocarbon refrigerants
RU2454453C2 (en) Refrigerator oil and refrigerator hydraulic fluid composition
JP2977971B2 (en) Lubrication method for compression refrigeration system
WO2024048658A1 (en) Refrigerating machine oil, working fluid composition, and refrigerant dissolution viscosity modifier
KR0154109B1 (en) Method for lubricating compression-type refrigerating cycle
CA2068781A1 (en) Fluid composition for compression refrigeration
MXPA01007381A (en) Refrigeration lubricant composition

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19970327

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB IT LI NL PT SE

A4 Supplementary search report drawn up and despatched

Effective date: 19990601

AK Designated contracting states

Kind code of ref document: A4

Designated state(s): AT BE CH DE DK ES FR GB IT LI NL PT SE

RIC1 Information provided on ipc code assigned before grant

Free format text: 6C 10M 129/08 A, 6C 10M 131/12 B, 6C 10M 169/04 B, 6C 10M 171/00 B, 6C 10M 169/04 J, 6C 10M 101:02 J, 6C 10M 105:06 J, 6C 10M 105:38 J, 6C 10M 107:02 J, 6C 10M 129:08 J, 6C 10M 131:12 J, 6C 10N 40:30 Z

17Q First examination report despatched

Effective date: 20000211

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20010301