EP1252278B1 - Refrigerant lubricant compositions comprising a foam-inducing additive - Google Patents
Refrigerant lubricant compositions comprising a foam-inducing additive Download PDFInfo
- Publication number
- EP1252278B1 EP1252278B1 EP01902469A EP01902469A EP1252278B1 EP 1252278 B1 EP1252278 B1 EP 1252278B1 EP 01902469 A EP01902469 A EP 01902469A EP 01902469 A EP01902469 A EP 01902469A EP 1252278 B1 EP1252278 B1 EP 1252278B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lubricant composition
- foam
- lubricant
- composition according
- ester
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 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
- C10M169/00—Lubricating 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
- C10M169/04—Mixtures of base-materials and additives
- C10M169/041—Mixtures of base-materials and additives the additives being macromolecular compounds only
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- 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
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- 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
- C10M105/02—Well-defined hydrocarbons
- C10M105/06—Well-defined hydrocarbons aromatic
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- 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
- C10M105/38—Esters of polyhydroxy compounds
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- 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
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- C10M147/00—Lubricating compositions characterised by the additive being a macromolecular compound containing halogen
- C10M147/04—Monomer containing carbon, hydrogen, halogen and oxygen
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- 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
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
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- C10M2203/06—Well-defined aromatic compounds
- C10M2203/065—Well-defined aromatic compounds used as base material
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- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
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- C10M2207/286—Esters of polymerised unsaturated acids
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- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/04—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical
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- C10M2209/06—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
- C10M2209/062—Vinyl esters of saturated carboxylic or carbonic acids, e.g. vinyl acetate
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- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/36—Release agents or mold release agents
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/38—Conveyors or chain belts
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/40—Generators or electric motors in oil or gas winning field
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/42—Flashing oils or marking oils
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/44—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 a lubricant composition and its use in refrigeration systems.
- CFCs disclosed in US 3,792,755 include trichloroethylene, dichlorodifluoromethane (R-12) and monochlorodifluoromethane (R-22).
- HFC hydrofluorocarbon gases
- suitable base fluids for such synthetic lubricant compositions are polyalkylene glycols, polyol esters, polyvinyl ethers and alkylbenzenes.
- Known foaming additives are silicon based, for example organosiloxanes or silicones.
- WO95/12649 discloses a lubricant composition comprising a synthetic polyol ester lubricant and a foam density-increasing additive for use in a refrigerator system with at least one compressor and a halocarbon refrigerant gas, preferably an HFC.
- the foam density-increasing additive is preferably a siloxane but may also be a halogenated aliphatic polymeric ester (for example Fluorad FC430 available from 3M) and is found to both increase the foam density and control vapour evolution from the compressor.
- EP 0590238 A1 discloses a compressor for compressing an HFC refrigerant which is characterised by the presence of a lubricant composition consisting of a pentaerythritol ester and a siloxane foaming additive wherein an oil foam layer is created during compressor operation to reduce compressor noise.
- JP10088173 A2 discloses lubricant compositions for refrigeration compressors for noise reduction comprising HFC refrigerants, ester oil lubricants with at least 2 ester bonds, a hydrolytic stabiliser, an antioxidant and 0.001 - 0.01 wt. % of silicone oils.
- silicon-containing foaming additives may not be suitable for all refrigerant systems as they are only partially miscible with the base oil of the lubricant composition. This may lead to separation of the silicon-containing additives in cold parts of the refrigeration system.
- the loss of the silicone-containing additives may also cause loss of foaming due to additive depletion, fouling of heat exchange surfaces and valve blockage.
- silicones present on metal surfaces prevent painting of such surfaces.
- the present invention provides a lubricant composition
- a lubricant composition comprising;
- partially halogenated we mean that at least one hydrogen atom of the alkyl group has been replaced by a halogen atom.
- at least one hydrogen atom in each of the carbon atoms of the alkyl group has been replaced by a halogen atom, more preferably all of the hydrogen atoms of the alkyl group have been replaced by halogen atoms so that R is a fully halogenated alkyl group.
- the halogen atom is a fluorine atom. Especially preferred is when fluorine atoms have replaced all of the hydrogen atoms of the alkyl group.
- the alkyl group, R may be branched or straight chained and it may be saturated or unsaturated.
- R preferably has 1 to 7 carbon atoms, more preferably 1 to 4 carbon atoms. Examples of preferred R include -CF 2 - -CF 2 CF 2 -,-CF(CF 3 )-, -CF(CF 3 )CF 2 -, -CF 2 CF 2 CF 2 - and -CF 2 CF 2 CF 2 CF 2 -.
- R can be chosen such that the polyether is a block, random or graft copolymer or a homopolymer.
- n is preferably in the range from 1 to 100, more preferably from 1 to 50. n may be the same or different for the R groups.
- An example of a preferred embodiment is X-O-(R 1 O) n1 -(R 2 O) n2 -Y where R 1 and R 2 are as defined for R but R 1 is different to R 2 .
- n1 and n2 may be the same or different.
- the polyether backbone has two end groups, X and Y. At least one of the end groups X and Y comprises at least one functionalised group.
- Types of functionalised groups include hydroxyl, ester, ethoxylated hydroxyl, ethoxylated ester, both organic and inorganic, amine, cyano, and amide.
- the or each functionalised group may be positioned on the end group so as to be directly linked to the polyether backbone; or it may be positioned at the extremity of the end group away from the polyether backbone; or it may be positioned within the backbone of the end group.
- the functionalised group is positioned at the extremity of the end group away from the polyether backbone.
- end groups that may be present within the or each end group include alkyl and haloalkyl, in particular fluoralkyl.
- the end group is such that it confers solubility of the foam-inducing additive in the synthetic lubricant base oil.
- Examples of end groups, which comprise a functionalised group are -CF 2 COOCH 3 , -CF 2 CH 2 OH, -CF 2 CH 2 O(CH 2 CH 2 O) n H and -CF 2 CH 2 OCH 2 CH(OH)CH 2 OH .
- the foam-inducing additive preferably has a molecular weight between 100 and 10000 atomic units, more preferably between 200 and 5000 atomic units. It is present at a level of between 0.0001 to 1.0% by weight in the lubricant composition, preferably at a level of between 0.0001 to 0.05%
- the synthetic lubricant base oil is selected such that the lubricant composition is compatible with HFC refrigerant gases.
- it is selected from alkylbenzenes, polyvinyl ethers, polyalkylene glycols and esters.
- the synthetic lubricant base oil is an ester; more preferably an ester which is a derivative of a polyol, preferably an aliphatic hydrocarbon-based polyol, having from 2 to 6 hydroxyl groups and, preferably, from 3 to 12 carbon atoms.
- Suitable polyols include neopentyl glycol, pentaerythritol, trimethylolpropane, ditrimethylolpropane and dipentaerythritol.
- the ester is derived from the reaction of such a polyol with one or more linear or branched, saturated or unsaturated monocarboxylic acids having from 3 to 12 carbon atoms and optionally one or more linear or branched, saturated or unsaturated polycarboxylic acids having from 4 to 54 carbon atoms.
- the polycarboxylic acids if present, have 2 or 3 carboxyl groups. All of the above acids may be replaced by their esterifiable derivatives, for example anhydrides.
- Suitable lubricant compositions include the EMKARATE RL range of refrigeration lubricants available from Uniqema, a business of Imperial Chemical Industries plc.
- the synthetic lubricant base oils for these lubricant compositions are derived from pentaerythritol or oligomers thereof and/or neopentyl glycol reacted with linear and/or branched acids (or their esterifiable derivatives) having from 5 to 10 carbon atoms.
- the synthetic lubricant base oil has a viscosity at 40°C from 2 to 500cSt.
- the lubricant composition has a viscosity at 40°C from 2 to 500cSt.
- the lubricant composition may further comprise other foaming additives, for example organosiloxanes or silicones. If present, such other foaming additives are at a level of between 0.0001 to 1.0% by weight in the lubricant composition, preferably at a level of between 0.0001 to 0.1%, more preferably at a level between 0.0001 to 0.05%.
- the lubricant composition may also comprise other functional lubricant additives.
- Suitable additives include antioxidants, antiwear additives, extreme pressure agents, acid scavengers, stabilisers, surfactants, viscosity index improvers, corrosion inhibitors, metal deactivators or passivators, lubricity improvers or oiliness agents and friction modifiers.
- the present invention provides for use of a lubricant composition in a refrigeration system wherein the lubricant composition comprises
- the refrigerant in the refrigerant system suitably comprises a hydrochlorofluorocarbon (HCFC), an HFC or a blend of refrigerants containing at least one HFC, HCFC or both.
- HCFC hydrochlorofluorocarbon
- the refrigerant does not contain any chlorine atoms.
- Suitable HFC gases include R134a (1,1,1,2-tetrafluoroethane), R-32 (difluoromethane), R-125 (1,1,1,2,2-pentafluoroethane), R-152a (1,1-difluoroethane) and R-143a (1,1,1-trifluoroethane).
- hydrocarbons preferably with 1 to 6 carbon atoms
- fluorinated hydrocarbons and other refrigerants for example carbon dioxide or ammonia.
- the foaming tendency and foam stability of 200mls of a lubricant composition comprising EMKARATE RL 22H ex ICI and various levels of foam-inducing additive, Fomblin HC-OH ex Ausimont (HOCH 2 CF 2 O-(CF 2 CF 2 O) p- (CF 2 O) q -CF 2 CH 2 OH), were measured at room temperature (24.5 °C).
- the foaming tendency of the lubricant composition was determined using the standard test method ASTM D-892-97, Standard Test Method for Foaming Characteristics of Lubricating Oils. The test determines the foam tendency in terms of the volume of foam produced by bubbling air through 200mls of the lubricant composition.
- the foam stability is the time taken in seconds for the foam to disappear.
- Example 1 was repeated except that R134a was bubbled through the lubricant composition instead of air. The results are shown in Table 2.
- Example 1 was repeated except the Fomblin HC-OH was replaced by Fluorolink E10 (H(OCH 2 CH 2 ) n OCH 2 CF 2 O-(CF 2 CF 2 O) p -(CF 2 O) q -CF 2 CH 2 O(CH 2 CH 2 O) n H) ex Ausimont. The results are shown in Table 3.
- Fomblin Y Lvac is a perfluoroalkylether of molecular weight about 2400 ex Ausimont .
- PDMS 1 is Silicone Fluid SWS-101 50 ex Akrochem of viscosity 50cSt.
- PDMS 2 is Silicone Fluid SWS-101 350 ex Akrochem of viscosity 350cSt.
- Fluorad FC430 is a fluorinated surfactant ex 3M.
- Example 1 was repeated using 250ppm Fomblin HC-OH and the addition of 120ppm of 50cSt Silicone Fluid SWS-101 50 ex Akrochem. The results are shown in Table 6. Table 6 Foam Inducing Additive (ppm) Foam Tendency in Air (ml) Foam Stability in Air (seconds) Fomblin HC-OH (250ppm) and Silicone (120ppm) 350 178 Silicone (120ppm) only - Comparative 150 78
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Abstract
Description
- This invention relates to a lubricant composition and its use in refrigeration systems.
- It is known that excessive foaming in refrigeration systems is undesirable. It reduces the lubricant composition's effectiveness in cooling the motor windings and removing heat from the compressor. Also too much foam can cause too much lubricant composition to pass through the system pump and enter the low-pressure side of the refrigeration system. However, a moderate amount of foaming can be beneficial, particularly for suppression of noise within the refrigeration system compressor. Section 7.20 of the 1998 ASHRAE Refrigeration Handbook states that "a foamy layer on top of the lubricant level dampens the noise created by the moving parts of the compressor". There are other benefits of foam creation; for example control of vapour release rate as disclosed in WO/9512649 and promotion of enhanced oil return as disclosed in US 4829786.
- Historically, mineral oils were used in lubricant compositions for chlorofluorocarbon (CFC) and hydrochlorofluorocarbon (HCFC) refrigerant gases. These lubricant composition/CFC/HCFC mixtures demonstrated a tendency to foam. In some cases in which foaming is undesirable or excessive it was found to be necessary to control foam production. In other instances, where foaming is advantageous, it was found necessary to promote foaming. For example, US 3,792,755 discloses a method of attenuating the noise produced by an operating hermetic compressor unit which has a means for agitating the lubricant composition during operation, which lubricant composition contains a foaming agent, which is an organosiloxane. The foaming agent assists in generating and sustaining a froth or foam of fine bubbles which acts to absorb and thus attenuate the noise produced by the compressor unit during operation. CFCs disclosed in US 3,792,755 include trichloroethylene, dichlorodifluoromethane (R-12) and monochlorodifluoromethane (R-22).
- In recent years, legislation has dictated a move away from such traditional refrigerant gases to alternatives having lower- or zero-ozone depletion potential, such as hydrofluorocarbon gases (HFC). This change in refrigerant gas has necessitated a change in lubricant composition away from mineral oils, which are not compatible with these new HFC gases. More polar, HFC-compatible, synthetic lubricant compositions are used. Examples of suitable base fluids for such synthetic lubricant compositions are polyalkylene glycols, polyol esters, polyvinyl ethers and alkylbenzenes.
- It has been found that mixtures of HFC refrigerant gases and such synthetic lubricant compositions tend to show a much lower inherent foaming tendency than CFC mixtures with mineral oil based lubricant compositions; for example see Chapter 5 of "Foaming Characteristics of Refrigerant/Lubricant Mixtures", reference number DOE/CE/23810-88a which reported work supported by the US Department of Energy and was prepared for The Air-Conditioning and Refrigeration Technology Institute in March 1998. Consequently, when foam generation is an advantage, there is a need to generate a froth or foam of fine bubbles in the lubricant composition. The generation of such foam can be achieved by the addition of a foaming additive to the lubricant composition.
- Known foaming additives are silicon based, for example organosiloxanes or silicones. WO95/12649 discloses a lubricant composition comprising a synthetic polyol ester lubricant and a foam density-increasing additive for use in a refrigerator system with at least one compressor and a halocarbon refrigerant gas, preferably an HFC. The foam density-increasing additive is preferably a siloxane but may also be a halogenated aliphatic polymeric ester (for example Fluorad FC430 available from 3M) and is found to both increase the foam density and control vapour evolution from the compressor.
- EP 0590238 A1 discloses a compressor for compressing an HFC refrigerant which is characterised by the presence of a lubricant composition consisting of a pentaerythritol ester and a siloxane foaming additive wherein an oil foam layer is created during compressor operation to reduce compressor noise.
- JP10088173 A2 discloses lubricant compositions for refrigeration compressors for noise reduction comprising HFC refrigerants, ester oil lubricants with at least 2 ester bonds, a hydrolytic stabiliser, an antioxidant and 0.001 - 0.01 wt. % of silicone oils.
- However, these silicon-containing foaming additives may not be suitable for all refrigerant systems as they are only partially miscible with the base oil of the lubricant composition. This may lead to separation of the silicon-containing additives in cold parts of the refrigeration system. The loss of the silicone-containing additives may also cause loss of foaming due to additive depletion, fouling of heat exchange surfaces and valve blockage. Furthermore silicones present on metal surfaces prevent painting of such surfaces.
- Hence alternative foaming additives are being sought.
- Accordingly, in a first aspect, the present invention provides a lubricant composition comprising;
- a) a synthetic lubricant base oil; and
- b) a foam-inducing additive, which comprises a polyether having the formula
X-O-(RO)n-Y
wherein- -O-(RO)n- is a polyether backbone
- R is a partially or fully halogenated alkyl group having 1 to 10 carbon atoms and wherein adjacent R groups may be the same or different
- n is in the range1 to 1000 and
- X and Y are end groups, as set forth in claim 1.
- By partially halogenated, we mean that at least one hydrogen atom of the alkyl group has been replaced by a halogen atom. Preferably at least one hydrogen atom in each of the carbon atoms of the alkyl group has been replaced by a halogen atom, more preferably all of the hydrogen atoms of the alkyl group have been replaced by halogen atoms so that R is a fully halogenated alkyl group. Preferably the halogen atom is a fluorine atom. Especially preferred is when fluorine atoms have replaced all of the hydrogen atoms of the alkyl group.
- The alkyl group, R, may be branched or straight chained and it may be saturated or unsaturated. R preferably has 1 to 7 carbon atoms, more preferably 1 to 4 carbon atoms. Examples of preferred R include -CF2- -CF2CF2-,-CF(CF3)-, -CF(CF3)CF2-, -CF2CF2CF2- and -CF2CF2CF2CF2-. R can be chosen such that the polyether is a block, random or graft copolymer or a homopolymer.
- n is preferably in the range from 1 to 100, more preferably from 1 to 50. n may be the same or different for the R groups.
- An example of a preferred embodiment is
X-O-(R1O)n1-(R2O)n2-Y
where R1 and R2 are as defined for R but R1 is different to R2. n1 and n2 may be the same or different. - The polyether backbone has two end groups, X and Y. At least one of the end groups X and Y comprises at least one functionalised group. Types of functionalised groups include hydroxyl, ester, ethoxylated hydroxyl, ethoxylated ester, both organic and inorganic, amine, cyano, and amide. The or each functionalised group may be positioned on the end group so as to be directly linked to the polyether backbone; or it may be positioned at the extremity of the end group away from the polyether backbone; or it may be positioned within the backbone of the end group. Preferably the functionalised group is positioned at the extremity of the end group away from the polyether backbone. Other groups that may be present within the or each end group include alkyl and haloalkyl, in particular fluoralkyl. Preferably the end group is such that it confers solubility of the foam-inducing additive in the synthetic lubricant base oil. Examples of end groups, which comprise a functionalised group, are -CF2COOCH3, -CF2CH2OH, -CF2CH2O(CH2CH2O)nH and -CF2CH2OCH2CH(OH)CH2OH .
- The foam-inducing additive preferably has a molecular weight between 100 and 10000 atomic units, more preferably between 200 and 5000 atomic units. It is present at a level of between 0.0001 to 1.0% by weight in the lubricant composition, preferably at a level of between 0.0001 to 0.05%
- The synthetic lubricant base oil is selected such that the lubricant composition is compatible with HFC refrigerant gases. Preferably, it is selected from alkylbenzenes, polyvinyl ethers, polyalkylene glycols and esters. Preferably the synthetic lubricant base oil is an ester; more preferably an ester which is a derivative of a polyol, preferably an aliphatic hydrocarbon-based polyol, having from 2 to 6 hydroxyl groups and, preferably, from 3 to 12 carbon atoms. Suitable polyols include neopentyl glycol, pentaerythritol, trimethylolpropane, ditrimethylolpropane and dipentaerythritol. The ester is derived from the reaction of such a polyol with one or more linear or branched, saturated or unsaturated monocarboxylic acids having from 3 to 12 carbon atoms and optionally one or more linear or branched, saturated or unsaturated polycarboxylic acids having from 4 to 54 carbon atoms. Preferably the polycarboxylic acids, if present, have 2 or 3 carboxyl groups. All of the above acids may be replaced by their esterifiable derivatives, for example anhydrides.
- Examples of suitable lubricant compositions include the EMKARATE RL range of refrigeration lubricants available from Uniqema, a business of Imperial Chemical Industries plc. The synthetic lubricant base oils for these lubricant compositions are derived from pentaerythritol or oligomers thereof and/or neopentyl glycol reacted with linear and/or branched acids (or their esterifiable derivatives) having from 5 to 10 carbon atoms.
- The synthetic lubricant base oil has a viscosity at 40°C from 2 to 500cSt.
- The lubricant composition has a viscosity at 40°C from 2 to 500cSt. The lubricant composition may further comprise other foaming additives, for example organosiloxanes or silicones. If present, such other foaming additives are at a level of between 0.0001 to 1.0% by weight in the lubricant composition, preferably at a level of between 0.0001 to 0.1%, more preferably at a level between 0.0001 to 0.05%. The lubricant composition may also comprise other functional lubricant additives. Suitable additives include antioxidants, antiwear additives, extreme pressure agents, acid scavengers, stabilisers, surfactants, viscosity index improvers, corrosion inhibitors, metal deactivators or passivators, lubricity improvers or oiliness agents and friction modifiers.
- In a second aspect, the present invention provides for use of a lubricant composition in a refrigeration system wherein the lubricant composition comprises
- a) a synthetic lubricant base oil; and
- b) a foam-inducing additive, which comprises a polyether having the formula
X-O-(RO)n-Y
wherein- -O-(RO)n- is a polyether backbone
- R is a partially or fully halogenated alkyl group having 1 to 10 carbon atoms and wherein adjacent R groups may be the same or different
- n is in the range1 to 1000 and
- X and Y are end groups, as set forth in claim 10.
- The refrigerant in the refrigerant system suitably comprises a hydrochlorofluorocarbon (HCFC), an HFC or a blend of refrigerants containing at least one HFC, HCFC or both. Preferably the refrigerant does not contain any chlorine atoms. Suitable HFC gases include R134a (1,1,1,2-tetrafluoroethane), R-32 (difluoromethane), R-125 (1,1,1,2,2-pentafluoroethane), R-152a (1,1-difluoroethane) and R-143a (1,1,1-trifluoroethane). There may be other components in the refrigerant blend, for example hydrocarbons, preferably with 1 to 6 carbon atoms, fluorinated hydrocarbons and other refrigerants, for example carbon dioxide or ammonia.
- The present invention is further illustrated with reference to the following non-limiting examples.
- The foaming tendency and foam stability of 200mls of a lubricant composition comprising EMKARATE RL 22H ex ICI and various levels of foam-inducing additive, Fomblin HC-OH ex Ausimont (HOCH2CF2O-(CF2CF2O)p-(CF2O)q-CF2CH2OH), were measured at room temperature (24.5 °C). The foaming tendency of the lubricant composition was determined using the standard test method ASTM D-892-97, Standard Test Method for Foaming Characteristics of Lubricating Oils. The test determines the foam tendency in terms of the volume of foam produced by bubbling air through 200mls of the lubricant composition. The foam stability is the time taken in seconds for the foam to disappear.
- The results are shown in Table 1.
- Example 1 was repeated except that R134a was bubbled through the lubricant composition instead of air. The results are shown in Table 2.
- Example 1 was repeated except the Fomblin HC-OH was replaced by Fluorolink E10 (H(OCH2CH2)nOCH2CF2O-(CF2CF2O)p-(CF2O)q-CF2CH2O(CH2CH2O)nH) ex Ausimont. The results are shown in Table 3.
Table 1 Concentration of Fomblin HC-OH (ppm) Foam Tendency (ml) Foam Stability (seconds) 0 0 0 20 20 0 50 380 135 100 380 219 250 400 206 500 370 220 Table 2 Concentration of Fomblin HC-OH (ppm) Foam Tendency (ml) Foam Stability (seconds) 0 0 0 20 0 0 50 40 35 100 30 27 250 20 10 500 30 19 Table 3 Concentration of Fluorolink E10 (ppm) Foam Tendency (ml) Foam Stability (seconds) 0 0 0 250 390 194 - The foaming tendency and foam stability of 200mls of a lubricant composition comprising various EMKARATE RL grades ex ICI and 250ppm foam-inducing additive Fomblin HC-OH were measured at room temperature (24.5 °C) by bubbling through both air and R134a. The results are shown in Table 4.
Table 4 EMKARATE RL Grade Foam Tendency in Air (ml) Foam Tendency in R134a (ml) Foam Stability in Air (seconds) Foam Stability in R134a (seconds) 32H 480 50 294 58 15H 230 50 112 21 7H 50 30 21 12 - The foaming tendency and foam stability of 200mls of a lubricant composition comprising EMKARATE RL 22H ex ICI and various foam-inducing additives were measured at room temperature (24.5 °C). The results are shown in Table 5.
Table 5 Foam Inducing Additive (ppm) Foam Tendency in Air (ml) Foam Stability in Air (seconds) Fomblin HC-OH (250ppm) 470 237 Fluorolink E10 (250ppm) 390 194 Fluorad FC430 (250ppm) (Comparative) 0 0 FS1265 (250ppm) (Comparative) 360 222 Fomblin Y Lvac (250ppm) (Comparative) 0 0 PDMS 1 (500ppm) (Comparative) 5 13 PDMS 2 (500ppm) (Comparative) 5 30 FS1265 is trifluoromethyl siloxane ex Dow.
Fomblin Y Lvac is a perfluoroalkylether of molecular weight about 2400 ex Ausimont .
PDMS 1 is Silicone Fluid SWS-101 50 ex Akrochem of viscosity 50cSt.
PDMS 2 is Silicone Fluid SWS-101 350 ex Akrochem of viscosity 350cSt.
Fluorad FC430 is a fluorinated surfactant ex 3M. - The results are indicative of superior foam tendency and stability of lubricant compositions of the present invention.
- Example 1 was repeated using 250ppm Fomblin HC-OH and the addition of 120ppm of 50cSt Silicone Fluid SWS-101 50 ex Akrochem. The results are shown in Table 6.
Table 6 Foam Inducing Additive (ppm) Foam Tendency in Air (ml) Foam Stability in Air (seconds) Fomblin HC-OH (250ppm) and Silicone (120ppm) 350 178 Silicone (120ppm) only - Comparative 150 78
Claims (10)
- A lubricant composition comprising;a) a synthetic lubricant base oil; andb) a foam-inducing additive, which comprises a polyether having the formula
X-O-(RO)n-Y
wherein-O-(RO)n- is a polyether backboneR is a partially or fully halogenated alkyl group having 1 to 10 carbon atoms and wherein adjacent R groups may be the same or differentn is in the range1 to 1000 andX and Y are end groups, wherein at least one of the end groups X and Y comprise at least one functionalised group selected from hydroxyl, ester, ethoxylated hydroxyl, ethoxylated ester, both organic and inorganic, amine, cyano and amide. - A lubricant composition according to claim 1 wherein R is a fully halogenated alkyl group having 1 to 7 carbon atoms.
- A lubricant composition according to claim 1 or claim 2 wherein the halogen is fluorine.
- A lubricant composition according to any one of claims 1 to 3 wherein n is in the range 1 to 100.
- A lubricant composition according to any one of claims 1 to 4 wherein the at least one functionalised group is positioned at the extremity of the end group away from the polyether backbone.
- .A lubricant composition according to any one of claims 1 to 5 wherein the at least one functionalised group includes haloalkyl groups.
- A lubricant composition according to any one of claims 1 to 6 wherein the foam-inducing additive is present at a level of between 0.0001 to 0.1% by weight of the lubricant composition.
- A lubricant composition according to any one of claims 1 to 7 wherein the synthetic lubricant base oil is chosen from alkylbenzenes, polyvinyl ethers, polyalkylene glycols and esters.
- A lubricant composition according to claim 8 wherein the synthetic lubricant base oil is an ester which is a derivative of a polyol.
- Use of a lubricant composition in a refrigeration system wherein the lubricant composition comprisesa) a synthetic lubricant base oil; andb) a foam-inducing additive, which comprises a polyether having the formula
X-O-(RO)n-Y
wherein-O-(RO)n- is a polyether backboneR is a partially or fully halogenated alkyl group having 1 to 10 carbon atoms and wherein adjacent R groups may be the same or differentn is in the range1 to 1000 andX and Y are end groups, wherein at least one of the end groups X and Y comprise at least one functionalised group selected from hydroxyl, ester, ethoxylated hydroxyl, ethoxylated ester, both organic and inorganic, amine, cyano and amide.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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GB0001981 | 2000-01-31 | ||
GBGB0001981.0A GB0001981D0 (en) | 2000-01-31 | 2000-01-31 | Refrigerant lubricant compositions |
PCT/GB2001/000255 WO2001057165A1 (en) | 2000-01-31 | 2001-01-24 | Refrigerant lubricant composition comprising a foam-inducing additive |
Publications (2)
Publication Number | Publication Date |
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EP1252278A1 EP1252278A1 (en) | 2002-10-30 |
EP1252278B1 true EP1252278B1 (en) | 2006-09-27 |
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EP01902469A Expired - Lifetime EP1252278B1 (en) | 2000-01-31 | 2001-01-24 | Refrigerant lubricant compositions comprising a foam-inducing additive |
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US (1) | US20030040445A1 (en) |
EP (1) | EP1252278B1 (en) |
JP (2) | JP2003522254A (en) |
KR (1) | KR100675248B1 (en) |
CN (1) | CN1210387C (en) |
AT (1) | ATE340840T1 (en) |
AU (1) | AU2001230330A1 (en) |
DE (1) | DE60123386D1 (en) |
ES (1) | ES2270978T3 (en) |
GB (1) | GB0001981D0 (en) |
MY (1) | MY136416A (en) |
TW (1) | TWI225515B (en) |
WO (1) | WO2001057165A1 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040089839A1 (en) | 2002-10-25 | 2004-05-13 | Honeywell International, Inc. | Fluorinated alkene refrigerant compositions |
US7098173B2 (en) * | 2002-11-19 | 2006-08-29 | General Motors Corporation | Thermally stable antifoam agent for use in automatic transmission fluids |
US8188323B2 (en) * | 2006-01-13 | 2012-05-29 | E.I. Du Pont De Nemours And Company | Refrigerant compositions containing perfluoropolyethers |
US7759532B2 (en) * | 2006-01-13 | 2010-07-20 | E.I. Du Pont De Nemours And Company | Refrigerant additive compositions containing perfluoropolyethers |
US20070187639A1 (en) * | 2006-01-13 | 2007-08-16 | Leck Thomas J | Refrigerant additive compositions containing perfluoropolethers |
WO2008027514A1 (en) | 2006-09-01 | 2008-03-06 | E. I. Du Pont De Nemours And Company | Terpene, terpenoid, and fullerene stabilizers for fluoroolefins |
JP2008266656A (en) * | 2008-07-04 | 2008-11-06 | Tonengeneral Sekiyu Kk | Lubricating oil composition |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
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US3597359A (en) * | 1968-03-22 | 1971-08-03 | Monsanto Co | Functional fluid compositions |
US3701733A (en) * | 1968-03-22 | 1972-10-31 | Monsanto Co | Functional fluid compositions |
US4174461A (en) * | 1970-06-27 | 1979-11-13 | Montecantini Edison S.P.A. | Stabilized perfluoropolyether fluids |
US3701732A (en) * | 1971-03-26 | 1972-10-31 | Monsanto Co | Functional fluid compositions |
US5190681A (en) * | 1988-04-13 | 1993-03-02 | Ausimont S.R.L. | Antirust additives for lubricants or greases based on perfluoropolyethers |
JPH06102723B2 (en) * | 1988-04-19 | 1994-12-14 | ダイキン工業株式会社 | Fluorine-containing polyether and fluorine-containing lubricant |
JPH03126790A (en) * | 1989-10-13 | 1991-05-29 | Nippon Oil Co Ltd | Lubricating oil composition |
IT1237887B (en) * | 1989-12-12 | 1993-06-18 | Ausimont Spa | PERFLUOROPOLIETEREI LUBRICANTS WITH WEAR PROPERTIES |
GB9205726D0 (en) * | 1992-03-16 | 1992-04-29 | British Petroleum Co Plc | Lubricating oil composition |
US5499908A (en) * | 1992-09-30 | 1996-03-19 | Tecumseh Products Company | Method of making foam in an energy efficient compressor |
WO1995012649A1 (en) * | 1993-11-06 | 1995-05-11 | Castrol Limited | Lubrication of refrigeration compressors |
JPH1088166A (en) * | 1996-09-20 | 1998-04-07 | Japan Energy Corp | Foam stabilizer for lubricating oil, refrigerating machine oil and fluid for operating refrigerating machine |
US6468947B1 (en) * | 1999-03-26 | 2002-10-22 | Seagate Technology Llc | Lubricants with improved stability for magnetic recording media |
-
2000
- 2000-01-31 GB GBGB0001981.0A patent/GB0001981D0/en not_active Ceased
-
2001
- 2001-01-24 KR KR1020027009794A patent/KR100675248B1/en active IP Right Grant
- 2001-01-24 CN CNB018043437A patent/CN1210387C/en not_active Expired - Lifetime
- 2001-01-24 EP EP01902469A patent/EP1252278B1/en not_active Expired - Lifetime
- 2001-01-24 WO PCT/GB2001/000255 patent/WO2001057165A1/en active IP Right Grant
- 2001-01-24 JP JP2001557984A patent/JP2003522254A/en not_active Withdrawn
- 2001-01-24 AU AU2001230330A patent/AU2001230330A1/en not_active Abandoned
- 2001-01-24 DE DE60123386T patent/DE60123386D1/en not_active Expired - Lifetime
- 2001-01-24 ES ES01902469T patent/ES2270978T3/en not_active Expired - Lifetime
- 2001-01-24 AT AT01902469T patent/ATE340840T1/en not_active IP Right Cessation
- 2001-01-30 MY MYPI20010392A patent/MY136416A/en unknown
- 2001-01-31 TW TW090101891A patent/TWI225515B/en not_active IP Right Cessation
-
2002
- 2002-07-30 US US10/207,178 patent/US20030040445A1/en not_active Abandoned
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2012
- 2012-02-06 JP JP2012022967A patent/JP5767130B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CN1210387C (en) | 2005-07-13 |
WO2001057165A1 (en) | 2001-08-09 |
GB0001981D0 (en) | 2000-03-22 |
AU2001230330A1 (en) | 2001-08-14 |
JP2012132014A (en) | 2012-07-12 |
JP5767130B2 (en) | 2015-08-19 |
ES2270978T3 (en) | 2007-04-16 |
TWI225515B (en) | 2004-12-21 |
CN1396949A (en) | 2003-02-12 |
MY136416A (en) | 2008-09-30 |
JP2003522254A (en) | 2003-07-22 |
ATE340840T1 (en) | 2006-10-15 |
KR20020068545A (en) | 2002-08-27 |
KR100675248B1 (en) | 2007-01-29 |
DE60123386D1 (en) | 2006-11-09 |
EP1252278A1 (en) | 2002-10-30 |
US20030040445A1 (en) | 2003-02-27 |
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