WO1998008911A1 - Refrigerant compositions - Google Patents

Refrigerant compositions Download PDF

Info

Publication number
WO1998008911A1
WO1998008911A1 PCT/GB1997/002197 GB9702197W WO9808911A1 WO 1998008911 A1 WO1998008911 A1 WO 1998008911A1 GB 9702197 W GB9702197 W GB 9702197W WO 9808911 A1 WO9808911 A1 WO 9808911A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
weight
refrigerant
hydrofluorocarbon
boiling point
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.)
Ceased
Application number
PCT/GB1997/002197
Other languages
French (fr)
Inventor
Richard Llewellyn Powell
Stuart Corr
Frederick Thomas Murphy
James David Morrison
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10799211&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO1998008911(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to JP10511356A priority Critical patent/JP2000516980A/en
Priority to AT97936797T priority patent/ATE208412T1/en
Priority to EP97936797A priority patent/EP0922075B1/en
Priority to AU39496/97A priority patent/AU3949697A/en
Priority to DE69708123T priority patent/DE69708123T2/en
Publication of WO1998008911A1 publication Critical patent/WO1998008911A1/en
Anticipated expiration legal-status Critical
Ceased 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
    • 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
    • C09K2205/22All components of a mixture being fluoro compounds
    • 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
    • C09K2205/34The mixture being non-azeotropic
    • 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
    • C09K2205/40Replacement mixtures
    • C09K2205/41Type R11

Definitions

  • This invention relates to compositions which are suitable for refrigeration applications and to the use of such compositions in heat transfer devices such as refrigeration and air conditioning systems.
  • the invention relates, in particular, to non-azeotropic refrigerant compositions which can be used in the applications currently satisfied by trichlorofluoromethane (refrigerant R-l 1).
  • Heat transfer devices of the mechanical compression type such as refrigerators, freezers, heat pumps and air conditioning systems are well known.
  • a refrigerant liquid of a suitable boiling point evaporates at low pressure taking heat from a neighbouring heat transfer fluid.
  • the resulting vapour is then compressed and passes to a condenser where it condenses and gives off heat to another heat transfer fluid.
  • the condensate is then returned through an expansion valve to the evaporator so completing the cycle.
  • the mechanical energy required for compressing the vapour and pumping the liquid may be provided by an electric motor or an internal combustion engine.
  • the properties preferred of a refrigerant include low toxicity, non-flammability, non-corrosivity, high stability and freedom from objectionable odour.
  • heat transfer devices have tended to use fully and partially halogenated chlorofluorocarbon refrigerants such as bromotrifluoromethane (refrigerant R-13B1), trichlorofluoromethane (refrigerant R-l 1), dichlorodifluoromethane (refrigerant R-l 2), chlorodifluoromethane (refrigerant R-22) and the azeotropic mixture of chlorodifluoromethane and chloropentafluoroethane (refrigerant R-l 15); the azeotrope being refrigerant R-502.
  • Refrigerant R-l 1 has been widely used in chillers.
  • non-azeotropic composition comprising a mixture of compounds having zero ozone depletion potentials which can be used, for example, in chillers as a replacement for refrigerant R-l 1.
  • the non-azeotropic composition of the invention can boil over a wide temperature range and this property can be exploited to increase the energy efficiency of the equipment in which the composition is used.
  • the composition of the invention can exhibit an advantageously high refrigeration capacity. According to the present invention there is provided a non-azeotropic (zeotropic) composition comprising:
  • (B) at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50°C.
  • the present invention also provides a heat transfer device, such as a chiller, comprising an evaporator, a condenser, a compressor and an expansion valve in which there is contained a refrigerant composition
  • a heat transfer device such as a chiller, comprising an evaporator, a condenser, a compressor and an expansion valve in which there is contained a refrigerant composition
  • a refrigerant composition comprising:
  • (B) at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50°C.
  • the zeotropic composition of the invention comprises at least two separate components.
  • the first component (component (A)) comprises at least one hydrofluorocarbon selected from 1,1,1,2-tetrafluoroethane (R-134a), 1,1,2,2-tetrafluoroethane (R-134) and 1, 1 -difluoroethane (R-152a) which have boiling points of about -26.5°C, -19.7°C and -24.7°C respectively.
  • component (A) is R-l 34a or a mixture thereof with R-134, and in an especially preferred embodiment component (A) is R-l 34a.
  • the second component (component (B)) comprises at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50°C.
  • the at least one hydrofluorocarbon making up component (B) has a boiling point in the range of from 5 to 40°C, particularly in the range of from 10 to 35°C, more particularly in the range of from 10 to 30°C and especially in the range of from 15 to 30°C.
  • component (B) may comprise a mixture of two or more hydrofluorocarbons, it will preferably comprise just one such compound. Suitable hydrofluorocarbons for component (B) may be selected from
  • the at least one hydrofluorocarbon making up component (B) is selected from R-245ca and R-356ffa and in
  • the amounts of the at least one hydrofluorocarbon selected from R-l 34a, R-134 and R-l 52a and of the at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50°C which are contained in the zeotropic composition of the invention may be va ⁇ ed within wide limits, but typically the composition will comprise from 1 to 60 % by weight of R-134a, R-134 and/or R-152a and from 40 to 99 % by weight of the hydrofluorocarbon(s) having a boiling point in the range of from 5 to 50°C
  • a preferred composition of the invention in terms of its suitability as a replacement for refrigerant R-l 1 is one comp ⁇ sing from 1 to 40 % by weight of R-l 34a and from 60 to 99 % by weight of a hydrofluorocarbon(s) having a boiling point in the range of from 5 to 40°C
  • a particularly preferred composition of the invention in terms of its suitability as a replacement for refrigerant R-l 1 is one comp ⁇ sing from 1 to 20 % by weight, more particularly from 5 to 15 % by weight, of R-l 34a and from 80 to 99 % by weight, more particularly from 85 to 95 % by weight, of a hydrofluorocarbon(s) having a boiling point in the range of from 5 to 40°C
  • composition of the invention in terms of its suitability as a replacement for refrigerant R-l 1 is one comprising about 5 % by weight of R-l 34a and about 95 % by weight of a hydrofluorocarbon(s) having a boiling point in the range of from 5 to 40°C.
  • composition of the invention in terms of its suitability as a replacement for refrigerant R-l 1 is one comprising about 10 % by weight of R-l 34a and about 90 % by weight of a hydrofluorocarbon(s) having a boiling point in the range off ⁇ om 5 to 40°C.
  • composition of the invention When the composition of the invention is to be used as a refrigerant, it may be combined with one or more hydrocarbons in an amount which is sufficient to allow the composition to transport a mineral oil or alkyl benzene type lubricant around a refrigeration circuit and return it to the compressor. In this way, inexpensive lubricants based on mineral oils or alkyl benzenes may be used to lubricate the compressor.
  • Suitable hydrocarbons for inclusion in the refrigerant composition of the invention are those containing from 2 to 6 carbon atoms, with hydrocarbons containing from 3 to 5 carbon atoms being preferred. Hydrocarbons that will not significantly alter the thermophysical properties of the refrigerant at the level at which they provide for oil transport, such as the linear and branched isomers of butane and pentane are particularly preferred, with pentane being especially preferred.
  • a hydrocarbon is included, it will preferably be present in an amount of from 1 to 10 % by weight on the total weight of the composition.
  • the refrigerant composition of the invention may also be used in combination with the types of lubricants which have been specially developed for use with hydrofluorocarbon based refrigerants.
  • Such lubricants include those comprising a polyoxyalkylene glycol base oil.
  • Suitable polyoxyalkylene glycols include hydroxyl group initiated polyoxyalkylene glycols, e.g. ethylene and/or propylene oxide oligomers/polymers initiated on mono- or polyhydric alcohols such as methanol, butanol, pentaerythritol and glycerol.
  • Such polyoxyalkylene glycols may also be end-capped with suitable terminal groups such as alkyl, e.g. methyl groups.
  • suitable terminal groups such as alkyl, e.g. methyl groups.
  • Another class of lubricants which have been developed for use with hydrofluorocarbon based refrigerants and which may be used in combination with the present refrigerant compositions are those comprising a neopentyl polyol ester base oil derived from the reaction of at least one neopentyl polyol and at least one aliphatic carboxylic acid or an esterifiable derivative thereof.
  • Suitable neopentyl polyols for the formation of the ester base oil include pentaerythritol, polypentaerythritols such as di- and tripentaerythritol, trimethylol alkanes such as trimethylol ethane and trimethylol propane, and neopentyl glycol.
  • the esters may be formed with linear and/or branched aliphatic carboxylic acids, such as linear and/or branched alkanoic acids. Preferred acids are selected from the C 5.8 , particularly the C 5 7 , linear alkanoic acids and the C 5 10 , particularly the C 5.9 , branched alkanoic acids.
  • a minor proportion of an aliphatic polycarboxylic acid e.g. an aliphatic dicarboxylic acid, may also be used in the synthesis of the ester in order to increase the viscosity thereof.
  • an aliphatic polycarboxylic acid e.g. an aliphatic dicarboxylic acid
  • the amount of the carboxylic acid(s) which is used in the synthesis will be sufficient to esterify all of the hydroxyl groups contained in the polyol, although residual hydroxyl functionality may be acceptable.
  • the temperature of the heat transfer fluid being cooled which may be air or water for example, drops fairly rapidly on first contacting the cold surfaces provided by the refrigerant evaporating in the evaporator owing to the large difference in temperature between that fluid and the evaporating refrigerant.
  • the temperature of the heat transfer fluid is progressively reduced as it passes along the length of the evaporator, there is a progressive reduction in the temperature differential between the fluid and the evaporating refrigerant and a consequent reduction in the heat transfer or cooling rate.
  • the refrigerant composition of the invention is a non-azeotropic (zeotropic) composition which tends to boil over a wide temperature range under constant pressure conditions so as to create a temperature glide in the evaporator which can be exploited to reduce the energy required to operate the heat transfer device, e.g. by making use of the Lorentz cycle.
  • One technique for exploiting the temperature glide involves the use of a heat transfer device equipped with a counter current flow evaporator and/or condenser in which the refrigerant and the heat transfer fluid are caused to flow counter currently to each other. With such an arrangement, it is possible to minimise the temperature difference between the evaporating and condensing refrigerant whilst maintaining a sufficiently high temperature difference between the refrigerant and the external fluid(s) to cause the required heat transfer to take place.
  • This increase in the energy efficiency can be optimised by using a zeotropic refrigerant composition which boils and condenses over a temperature range which is equal or approximately equal to the temperature change to which the heat transfer fluid is to be subjected as it flows through the evaporator and condenser.
  • the zeotropic composition of the present invention may be used to provide the desired cooling in heat transfer devices such as chillers by a method which involves condensing the composition and thereafter evaporating it in a heat exchange relationship with a heat transfer fluid to be cooled.
  • the composition of the invention may be employed as a replacement for refrigerant R-l 1 in chillers.
  • composition of the invention may also be used as an aerosol propellant, as a foam blowing agent for blowing polyolefin, polyurethane and related foams, or as a solvent in degreasing or extraction applications.
  • aerosol propellant for blowing polyolefin, polyurethane and related foams
  • solvent in degreasing or extraction applications.
  • the evaluation involved first defining the inlet and outlet temperatures of the heat transfer fluid, which could be air or water for example, at each heat exchanger (evaporator and condenser)
  • the temperatures in the evaporator and condenser assuming that a pure (single component) refrigerant was used in the cycle, were then chosen and these temperatures together with the inlet and outlet temperatures of the heat transfer fluid referred to above were used to determine a target log mean temperature difference for each heat exchanger
  • the refrigerant inlet and outlet temperatures at both the evaporator and condenser were adjusted until the target log mean temperature difference was achieved for each heat exchanger When the target log mean temperature difference for each heat exchanger was achieved, the various properties of the refrigerant composition in the cycle were recorded
  • a composition comprising 75 % by weight R-l 34a and 25 % by weight R-245ca
  • composition comprising 50 % by weight R-l 34a and 50 % by weight R-245ca
  • composition comprising 25 % by weight R-134a and 75 % by weight R-245ca
  • composition comprising 10 % by weight R- 134a and 90 % by weight R-245ca (5) A composition comprising 5 % by weight R-l 34a and 95 % by weight R-245ca
  • R-l 34a and R-245ca boil over a wide temperature range in the evaporator and condense over a wide temperature range in the condenser, i.e. they exhibit wide glide behaviour in both heat exchangers, and that this property can enhance the energy efficiency of the refrigeration process as is evident from the higher values recorded for the coefficient of performance for most of the refrigerant compositions of the invention as compared to R-l 34a or R-245ca alone.
  • Table 1 also shows that the energy efficiency (coefficient of performance) reaches a maximum for a refrigerant composition containing around 10 % by weight R-l 34a, since such a composition exhibits temperature glides in the evaporator and condenser (8 15°C and 10 15°C respectively) which closely match the change in temperature expe ⁇ enced by the heat transfer fluid on passing through the evaporator and condenser (8°C and 10°C respectively)
  • a composition comprising 75 % by weight R-134a and 25 % by weight R-356ffa
  • composition comprising 50 % by weight R-134a and 50 % by weight R-356ffa
  • a composition comprising 25 % by weight R-l 34a and 75 % by weight R-356ffa
  • a composition comprising 5 % by weight R-l 34a and 95 % by weight R-356ffa
  • Table 2 also shows that the energy efficiency (coefficient of performance) reaches a maximum for a refrigerant composition containing around 10 % by weight R-l 34a, since such a composition exhibits temperature glides in the evaporator and condenser (8.41°C and 12.26°C respectively) which closely match the change in temperature experienced by the heat transfer fluid on passing through the evaporator and condenser (8°C and 10°C respectively).

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Combustion & Propulsion (AREA)
  • Thermal Sciences (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Thermotherapy And Cooling Therapy Devices (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

Abstract

A non-azeotropic (zeotropic) composition comprising (A) at least one hydrofluorocarbon selected from the group consisting of 1,1,1,2-tetrafluoroethane (R-134a), 1,1,2,2-tetrafluoroethane (R-134) and 1,1-difluoroethane (R-152a) and (B) at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50 °C is described. The composition is useful as a refrigerant and may be used in chillers as a replacement for refrigerant R-11.

Description

REFRIGERANT COMPOSITIONS
This invention relates to compositions which are suitable for refrigeration applications and to the use of such compositions in heat transfer devices such as refrigeration and air conditioning systems. The invention relates, in particular, to non-azeotropic refrigerant compositions which can be used in the applications currently satisfied by trichlorofluoromethane (refrigerant R-l 1).
Heat transfer devices of the mechanical compression type such as refrigerators, freezers, heat pumps and air conditioning systems are well known. In such devices a refrigerant liquid of a suitable boiling point evaporates at low pressure taking heat from a neighbouring heat transfer fluid. The resulting vapour is then compressed and passes to a condenser where it condenses and gives off heat to another heat transfer fluid. The condensate is then returned through an expansion valve to the evaporator so completing the cycle. The mechanical energy required for compressing the vapour and pumping the liquid may be provided by an electric motor or an internal combustion engine.
In addition to having a suitable boiling point and a high latent heat of vaporisation, the properties preferred of a refrigerant include low toxicity, non-flammability, non-corrosivity, high stability and freedom from objectionable odour. Hitherto, heat transfer devices have tended to use fully and partially halogenated chlorofluorocarbon refrigerants such as bromotrifluoromethane (refrigerant R-13B1), trichlorofluoromethane (refrigerant R-l 1), dichlorodifluoromethane (refrigerant R-l 2), chlorodifluoromethane (refrigerant R-22) and the azeotropic mixture of chlorodifluoromethane and chloropentafluoroethane (refrigerant R-l 15); the azeotrope being refrigerant R-502. Refrigerant R-l 1, for example, has been widely used in chillers.
However, the fully halogenated chlorofluorocarbons in particular have been implicated in the destruction of the earth's protective ozone layer and as a result the use and production thereof has been limited by international agreement. Whilst heat transfer devices of the type to which the present invention relates are essentially closed systems, loss of refrigerant to the atmosphere can occur due to leakage during operation of the equipment or during maintenance procedures. It is important, therefore, to replace fully halogenated chlorofluorocarbon refrigerants by materials having low or zero ozone depletion potentials.
In addition to the possibility of ozone depletion, it has been suggested that significant concentrations of chlorofluorocarbon refrigerants in the atmosphere might contribute to global warming (the so-called greenhouse effect). It is desirable, therefore, to use refrigerants which have relatively short atmospheric lifetimes as a result of their ability to react with other atmospheric constituents such as hydroxyl radicals.
Replacements for some of the chlorofluorocarbon refrigerants presently in use have already been developed. These replacement refrigerants tend to comprise selected hydrofluoroalkanes, i.e. compounds which contain only carbon, hydrogen and fluorine atoms in their structure. Thus, refrigerant R-12 is generally being replaced by 1,1, 1, 2-tetrafluoroethane (R- 134a) .
Although suitable replacement refrigerants are available, there is always a need for new refrigerants having a low or zero ozone depletion potential that are capable of replacing the chlorofluorocarbon refrigerants presently in use such as R-l 1 Furthermore, very re benefits could be realised by a new replacement refrigerant having a higher refrigeration capacity than the chlorofluorocarbon refrigerant it is replacing. It could also be beneficial in certain heat transfer devices to replace the chlorofluorocarbon refrigerant with a non-azeotropic refrigerant blend which not only exhibits a zero ozone depletion potential but which also boils over a reasonably wide temperature range, since in this way the energy efficiency (coefficient of performance) of the device may be increased leading to a reduction in indirect global warming. The present invention provides a non-azeotropic composition comprising a mixture of compounds having zero ozone depletion potentials which can be used, for example, in chillers as a replacement for refrigerant R-l 1. The non-azeotropic composition of the invention can boil over a wide temperature range and this property can be exploited to increase the energy efficiency of the equipment in which the composition is used. In addition, the composition of the invention can exhibit an advantageously high refrigeration capacity. According to the present invention there is provided a non-azeotropic (zeotropic) composition comprising:
(A) at least one hydrofluorocarbon selected from the group consisting of 1, 1, 1,2-tetrafluoroethane (R-134a), 1, 1,2,2-tetrafluoroethane (R-134) and 1, l-difluoroetlrane (R-l 52a); and
(B) at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50°C.
The present invention also provides a heat transfer device, such as a chiller, comprising an evaporator, a condenser, a compressor and an expansion valve in which there is contained a refrigerant composition comprising:
(A) at least one hydrofluorocarbon selected from the group consisting of 1, 1, 1,2-tetrafluoroethane (R-l 34a), 1,1,2,2-tetrafluoroethane (R-134) and 1 , 1 -difluoroethane (R- 152a); and
(B) at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50°C.
The zeotropic composition of the invention comprises at least two separate components.
The first component (component (A)) comprises at least one hydrofluorocarbon selected from 1,1,1,2-tetrafluoroethane (R-134a), 1,1,2,2-tetrafluoroethane (R-134) and 1, 1 -difluoroethane (R-152a) which have boiling points of about -26.5°C, -19.7°C and -24.7°C respectively. Preferably component (A) is R-l 34a or a mixture thereof with R-134, and in an especially preferred embodiment component (A) is R-l 34a. The second component (component (B)) comprises at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50°C. In a preferred embodiment, the at least one hydrofluorocarbon making up component (B) has a boiling point in the range of from 5 to 40°C, particularly in the range of from 10 to 35°C, more particularly in the range of from 10 to 30°C and especially in the range of from 15 to 30°C. Although component (B) may comprise a mixture of two or more hydrofluorocarbons, it will preferably comprise just one such compound. Suitable hydrofluorocarbons for component (B) may be selected from
1, 1, 2,2,3 -pentafluoropropane (R-245ca) which has a boiling point of about 25°C, 1,1,1,3,3-pentafluoropropane (R-245fa) which has a boiling point of about 15°C, 1,1,1, 2,2,3, 3,4,4-nonafluorobutane (R-329ccb) which has a boiling point of about 15°C, 1,1, 1,2,2,3-hexafluoropropane (R-236cb) which has a boiling point of about 15°C, 1,1,1,2,2,4,4,4-octafluorobutane (R-338cfa) which has a boiling point of about 18°C, and 1,1,1,4,4,4-hexafluorobutane (R-356fFa) which has a boiling point of about 26°C In a preferred embodiment, the at least one hydrofluorocarbon making up component (B) is selected from R-245ca and R-356ffa and in a particularly preferred embodiment component (B) is R-245ca
It is apparent that the boiling points of R-l 34a, R-134 and R-l 52a from which component (A) is selected are appreciably lower than the boiling point of the at least one hydrofluorocarbon making up component (B) which means that the composition of the invention is capable of boiling and condensing over a wide temperature range, i e it can exhibit a wide temperature glide in both the evaporator and condenser
The amounts of the at least one hydrofluorocarbon selected from R-l 34a, R-134 and R-l 52a and of the at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50°C which are contained in the zeotropic composition of the invention may be vaπed within wide limits, but typically the composition will comprise from 1 to 60 % by weight of R-134a, R-134 and/or R-152a and from 40 to 99 % by weight of the hydrofluorocarbon(s) having a boiling point in the range of from 5 to 50°C A preferred composition of the invention in terms of its suitability as a replacement for refrigerant R-l 1 is one compπsing from 1 to 40 % by weight of R-l 34a and from 60 to 99 % by weight of a hydrofluorocarbon(s) having a boiling point in the range of from 5 to 40°C
A particularly preferred composition of the invention in terms of its suitability as a replacement for refrigerant R-l 1 is one compπsing from 1 to 20 % by weight, more particularly from 5 to 15 % by weight, of R-l 34a and from 80 to 99 % by weight, more particularly from 85 to 95 % by weight, of a hydrofluorocarbon(s) having a boiling point in the range of from 5 to 40°C
An especially preferred composition of the invention in terms of its suitability as a replacement for refrigerant R-l 1 is one comprising about 5 % by weight of R-l 34a and about 95 % by weight of a hydrofluorocarbon(s) having a boiling point in the range of from 5 to 40°C.
Another especially preferred composition of the invention in terms of its suitability as a replacement for refrigerant R-l 1 is one comprising about 10 % by weight of R-l 34a and about 90 % by weight of a hydrofluorocarbon(s) having a boiling point in the range offτom 5 to 40°C.
When the composition of the invention is to be used as a refrigerant, it may be combined with one or more hydrocarbons in an amount which is sufficient to allow the composition to transport a mineral oil or alkyl benzene type lubricant around a refrigeration circuit and return it to the compressor. In this way, inexpensive lubricants based on mineral oils or alkyl benzenes may be used to lubricate the compressor.
Suitable hydrocarbons for inclusion in the refrigerant composition of the invention are those containing from 2 to 6 carbon atoms, with hydrocarbons containing from 3 to 5 carbon atoms being preferred. Hydrocarbons that will not significantly alter the thermophysical properties of the refrigerant at the level at which they provide for oil transport, such as the linear and branched isomers of butane and pentane are particularly preferred, with pentane being especially preferred.
Where a hydrocarbon is included, it will preferably be present in an amount of from 1 to 10 % by weight on the total weight of the composition. The refrigerant composition of the invention may also be used in combination with the types of lubricants which have been specially developed for use with hydrofluorocarbon based refrigerants. Such lubricants include those comprising a polyoxyalkylene glycol base oil. Suitable polyoxyalkylene glycols include hydroxyl group initiated polyoxyalkylene glycols, e.g. ethylene and/or propylene oxide oligomers/polymers initiated on mono- or polyhydric alcohols such as methanol, butanol, pentaerythritol and glycerol. Such polyoxyalkylene glycols may also be end-capped with suitable terminal groups such as alkyl, e.g. methyl groups. Another class of lubricants which have been developed for use with hydrofluorocarbon based refrigerants and which may be used in combination with the present refrigerant compositions are those comprising a neopentyl polyol ester base oil derived from the reaction of at least one neopentyl polyol and at least one aliphatic carboxylic acid or an esterifiable derivative thereof. Suitable neopentyl polyols for the formation of the ester base oil include pentaerythritol, polypentaerythritols such as di- and tripentaerythritol, trimethylol alkanes such as trimethylol ethane and trimethylol propane, and neopentyl glycol. The esters may be formed with linear and/or branched aliphatic carboxylic acids, such as linear and/or branched alkanoic acids. Preferred acids are selected from the C5.8, particularly the C5 7, linear alkanoic acids and the C5 10, particularly the C5.9, branched alkanoic acids. A minor proportion of an aliphatic polycarboxylic acid, e.g. an aliphatic dicarboxylic acid, may also be used in the synthesis of the ester in order to increase the viscosity thereof. Usu-ally, the amount of the carboxylic acid(s) which is used in the synthesis will be sufficient to esterify all of the hydroxyl groups contained in the polyol, although residual hydroxyl functionality may be acceptable.
The single component refrigerants and azeotropic refrigerant blends which are used in conventional heat transfer devices boil at a constant temperature in the evaporator under constant pressure conditions, and so produce an essentially constant temperature profile across the evaporator. The temperature of the heat transfer fluid being cooled, which may be air or water for example, drops fairly rapidly on first contacting the cold surfaces provided by the refrigerant evaporating in the evaporator owing to the large difference in temperature between that fluid and the evaporating refrigerant. However, since the temperature of the heat transfer fluid is progressively reduced as it passes along the length of the evaporator, there is a progressive reduction in the temperature differential between the fluid and the evaporating refrigerant and a consequent reduction in the heat transfer or cooling rate.
In contrast, the refrigerant composition of the invention is a non-azeotropic (zeotropic) composition which tends to boil over a wide temperature range under constant pressure conditions so as to create a temperature glide in the evaporator which can be exploited to reduce the energy required to operate the heat transfer device, e.g. by making use of the Lorentz cycle. One technique for exploiting the temperature glide involves the use of a heat transfer device equipped with a counter current flow evaporator and/or condenser in which the refrigerant and the heat transfer fluid are caused to flow counter currently to each other. With such an arrangement, it is possible to minimise the temperature difference between the evaporating and condensing refrigerant whilst maintaining a sufficiently high temperature difference between the refrigerant and the external fluid(s) to cause the required heat transfer to take place.
The consequence of minimising the temperature difference between the evaporating and condensing refrigerant in the same system is that the pressure difference is also minimised. As a result, the overall energy efficiency of the system is improved as less energy is consumed to bring about the refrigerant pressure rise from evaporator to condenser conditions.
This increase in the energy efficiency can be optimised by using a zeotropic refrigerant composition which boils and condenses over a temperature range which is equal or approximately equal to the temperature change to which the heat transfer fluid is to be subjected as it flows through the evaporator and condenser.
The zeotropic composition of the present invention may be used to provide the desired cooling in heat transfer devices such as chillers by a method which involves condensing the composition and thereafter evaporating it in a heat exchange relationship with a heat transfer fluid to be cooled. In particular, the composition of the invention may be employed as a replacement for refrigerant R-l 1 in chillers.
In addition to its use as a refrigerant, the composition of the invention may also be used as an aerosol propellant, as a foam blowing agent for blowing polyolefin, polyurethane and related foams, or as a solvent in degreasing or extraction applications. The present invention is now illustrated but not limited with reference to the following examples.
Example 1
The performance of five refrigerant compositions of the invention in a refrigeration cycle was evaluated using standard refrigeration cycle analysis techniques in order to assess the suitability thereof as a replacement for R-l 1. The operating conditions which were used for the analysis were chosen as being typical of those conditions which are found in a chiller or air conditioning system, and counter current flow at the heat exchangers was assumed. The evaluation involved first defining the inlet and outlet temperatures of the heat transfer fluid, which could be air or water for example, at each heat exchanger (evaporator and condenser) The temperatures in the evaporator and condenser, assuming that a pure (single component) refrigerant was used in the cycle, were then chosen and these temperatures together with the inlet and outlet temperatures of the heat transfer fluid referred to above were used to determine a target log mean temperature difference for each heat exchanger In the cycle analysis itself, the refrigerant inlet and outlet temperatures at both the evaporator and condenser were adjusted until the target log mean temperature difference was achieved for each heat exchanger When the target log mean temperature difference for each heat exchanger was achieved, the various properties of the refrigerant composition in the cycle were recorded
The following refrigerant compositions were subjected to the cycle analysis
(1) A composition comprising 75 % by weight R-l 34a and 25 % by weight R-245ca
(2) A composition comprising 50 % by weight R-l 34a and 50 % by weight R-245ca
(3) A composition comprising 25 % by weight R-134a and 75 % by weight R-245ca
(4) A composition comprising 10 % by weight R- 134a and 90 % by weight R-245ca (5) A composition comprising 5 % by weight R-l 34a and 95 % by weight R-245ca
The following operating conditions were used in the cycle analysis
EVAPORATOR
Evaporator Temperature- 5°C
Inlet Temperature of Heat Transfer Fluid 20°C
Outlet Temperature of Heat Transfer Fluid 12°C
Log Mean Temperature Difference for Evaporator 10 5°C CONDENSER:
Condenser Temperature: 32°C
Inlet Temperature of Heat Transfer Fluid 20°C Outlet Temperature of Heat Transfer Fluid 30°C
Log Mean Temperature Difference for Condenser 5.58°C
Amount of Superheat: 5°C
Amount of Subcooling: 5°C Isentropic Compressor Efficiency: 75 % Volumetric Flow through Compressor 1 m3/s
The results of analysing the performance of the five refrigerant compositions in a refrigeration cycle using these operating conditions are given in Table 1. The performance parameters of the refrigerant compositions which are presented in
Table 1 and in Table 2, i.e. condenser pressure, evaporator pressure, discharge temperature, refrigeration capacity (by which is meant the cooling duty achieved per unit swept volume of the compressor), coefficient of performance (COP) (by which is meant the ratio of cooling duty achieved to mechanical energy supplied to the compressor), and the glides in the evaporator and condenser (the temperature range over which the refrigerant composition boils in the evaporator and condenses in the condenser), are all art recognised parameters.
The performance of refrigerant R-l 1 under the same operating conditions is also shown in Table 1 by way of comparison. It is apparent from Table 1 that refrigerant compositions of the invention containing
R-l 34a and R-245ca boil over a wide temperature range in the evaporator and condense over a wide temperature range in the condenser, i.e. they exhibit wide glide behaviour in both heat exchangers, and that this property can enhance the energy efficiency of the refrigeration process as is evident from the higher values recorded for the coefficient of performance for most of the refrigerant compositions of the invention as compared to R-l 34a or R-245ca alone. Table 1 also shows that the energy efficiency (coefficient of performance) reaches a maximum for a refrigerant composition containing around 10 % by weight R-l 34a, since such a composition exhibits temperature glides in the evaporator and condenser (8 15°C and 10 15°C respectively) which closely match the change in temperature expeπenced by the heat transfer fluid on passing through the evaporator and condenser (8°C and 10°C respectively)
It is also apparent from Table 1 that refrigerant compositions of the invention containing R-l 34a and R-245ca have a higher refrigeration capacity than R-l 1 and comparable or lower discharge temperatures Moreover, for compositions containing 5 and 10 % by weight R-l 34a the evaporator and condenser pressures are comparable to R-l l
It is further evident from the results given in Table 1 that the performance of refrigerant compositions of the invention containing R-134a and R-245ca is such that they could make an acceptable replacement for refrigerant R-l l
Example 2
The performance of five refrigerant compositions of the invention in a refrigeration cycle was evaluated using exactly the same technique and exactly the same operating conditions as descπbed in Example 1
The following refrigerant compositions were subjected to the cycle analysis
(1) A composition comprising 75 % by weight R-134a and 25 % by weight R-356ffa
(2) A composition comprising 50 % by weight R-134a and 50 % by weight R-356ffa (3) A composition comprising 25 % by weight R-l 34a and 75 % by weight R-356ffa
(4) A composition compπsing 10 % by weight R- 134a and 90 % by weight R-356ffa
(5) A composition comprising 5 % by weight R-l 34a and 95 % by weight R-356ffa
The results of analysing the performance of these five refrigerant compositions in a refrigeration cycle are given in Table 2 The performance of refrigerant R-l 1 under the same operating conditions is also shown in Table 2 by way of comparison.
It is apparent from Table 2 that refrigerant compositions of the invention containing R-l 34a and R-356ffa boil over a wide temperature range in the evaporator and condense over a wide temperature range in the condenser, i.e. they exhibit wide glide behaviour in both heat exchangers, and that this property can enhance the energy efficiency of the refrigeration process as is evident from the higher values recorded for the coefficient of performance for the refrigerant compositions of the invention as compared to R-l 34a or R-356ffa alone. Table 2 also shows that the energy efficiency (coefficient of performance) reaches a maximum for a refrigerant composition containing around 10 % by weight R-l 34a, since such a composition exhibits temperature glides in the evaporator and condenser (8.41°C and 12.26°C respectively) which closely match the change in temperature experienced by the heat transfer fluid on passing through the evaporator and condenser (8°C and 10°C respectively).
It is also apparent from Table 2 that the refrigerant compositions tested had a higher refrigeration capacity than R-l 1 and lower discharge temperatures. Moreover, for compositions containing 5 and 10 % by weight R-l 34a the evaporator and condenser pressures are comparable to R-l 1. It is further evident from the results given in Table 2 that the performance of refrigerant compositions of the invention containing R-l 34a and R-356ffa is such that they could make an acceptable replacement for refrigerant R-l l.
TABLE 1
Figure imgf000014_0001
TABLE 2
Figure imgf000015_0001

Claims

Claims:
1. A non-azeotropic composition comprising:
(A) at least one hydrofluorocarbon selected from the group consisting of 1,1,1 ,2-tetrafluoroethane (R- 134a), 1 , 1 ,2,2-tetrafluoroethane (R- 134) and
1,1 -difluoroethane (R-l 52a); and
(B) at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50°C.
2. A composition as claimed in claim 1 comprising: (A) from 1 to 60 % by weight of at least one hydrofluorocarbon selected from the group consisting of R- 134a, R-134 and R-l 52a; and
(B) from 40 to 99 % by weight of at least one hydrofluorocarbon having a boiling point in the range of from 5 to 50°C.
3. A composition as claimed in claim 1 or claim 2, wherein component (A) is R-l 34a and component (B) consists of at least one hydrofluorocarbon having a boiling point in the range of from 5 to 40°C.
4. A composition as claimed in claim 3 comprising.
(A) from 1 to 40 % by weight of R-l 34a; and
(B) from 60 to 99 % by weight of at least one hydrofluorocarbon having a boiling point in the range of from 5 to 40°C.
5. A composition as claimed in claim 4 comprising:
(A) from 1 to 20 % by weight of R-134a; and
(B) from 80 to 99 % by weight of at least one hydrofluorocarbon having a boiling point in the range of from 5 to 40°C.
6. A composition as claimed in claim 5 comprising:
(A) from 5 to 15 % by weight of R-l 34a; and
(B) from 85 to 95 % by weight of at least one hydrofluorocarbon having a boiling point in the range of from 5 to 40°C.
7. A composition as claimed in claim 6 comprising: (A) about 5 % by weight of R-l 34a; and (B) about 95 % by weight of at least one hydrofluorocarbon having a boiling point in the range of from 5 to 40°C.
8. A composition as claimed in claim 6 comprising: (A) about 10 % by weight of R-l 34a; and (B) about 90 % by weight of at least one hydrofluorocarbon having a boiling point in the range of from 5 to 40°C.
9. A composition as claimed in any one of claims 3 to 8, wherein component (B) consists of at least one hydrofluorocarbon selected from the group consisting of 1,1, 2,2,3 -pentafluoropropane (R-245ca), 1,1, 1,3,3-pentafluoropropane (R-245fa), 1, 1, 1,2,2,3,3,4,4-nonafluorobutane (R-329ccb), 1,1,1,2,2,3-hexafluoropropane, (R-236cb), 1,1,1,2,2,4,4,4-octafluorobutane (R-338cfa), and 1, 1, 1 ,4,4,4-hexafluorobutane (R-356fFa).
10. A composition as claimed in claim 9, wherein component (B) consists of at least one hydrofluorocarbon selected from the group consisting of R-245ca and R-356fFa.
11. A composition as claimed in claim 10, wherein component (B) is R-245ca.
12. A composition as claimed in any one of the preceding claims which additionally comprises at least one hydrocarbon.
13. A composition as claimed in claim 12, wherein the at least one hydrocarbon comprises pentane.
14. A composition as claimed in claim 12 or claim 13 wherein the hydrocarbon is present in an amount of from 1 to 10 % by weight on the total weight of the composition.
15. A heat transfer device containing a composition as claimed in any one of claims 1 to 14.
16. A method for providing cooling which comprises condensing a composition as claimed in any one of claims 1 to 14 and thereafter evaporating it in a heat exchange relationship with a heat transfer fluid to be cooled.
17. The use of a composition as claimed in any one of claims 1 to 14 as a replacement for refrigerant R-l l .
PCT/GB1997/002197 1996-08-30 1997-08-18 Refrigerant compositions Ceased WO1998008911A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP10511356A JP2000516980A (en) 1996-08-30 1997-08-18 Refrigerant composition
AT97936797T ATE208412T1 (en) 1996-08-30 1997-08-18 COOLANT COMPOSITIONS
EP97936797A EP0922075B1 (en) 1996-08-30 1997-08-18 Refrigerant compositions
AU39496/97A AU3949697A (en) 1996-08-30 1997-08-18 Refrigerant compositions
DE69708123T DE69708123T2 (en) 1996-08-30 1997-08-18 COOLANT COMPOSITIONS

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9618180.5 1996-08-30
GBGB9618180.5A GB9618180D0 (en) 1996-08-30 1996-08-30 Refrigerant compositions

Publications (1)

Publication Number Publication Date
WO1998008911A1 true WO1998008911A1 (en) 1998-03-05

Family

ID=10799211

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB1997/002197 Ceased WO1998008911A1 (en) 1996-08-30 1997-08-18 Refrigerant compositions

Country Status (8)

Country Link
EP (1) EP0922075B1 (en)
JP (1) JP2000516980A (en)
AT (1) ATE208412T1 (en)
AU (1) AU3949697A (en)
DE (1) DE69708123T2 (en)
ES (1) ES2167012T3 (en)
GB (1) GB9618180D0 (en)
WO (1) WO1998008911A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4132209B2 (en) * 1998-04-30 2008-08-13 出光興産株式会社 Fluid composition for refrigerator
US20060179852A1 (en) * 2005-02-16 2006-08-17 Honeywell International Inc. Compositions and methods for cleaning vapor compression systems
JPWO2012161325A1 (en) * 2011-05-25 2014-07-31 東芝キヤリア株式会社 Heating device
US9039923B2 (en) 2012-02-14 2015-05-26 United Technologies Corporation Composition of zeotropic mixtures having predefined temperature glide

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0433989A (en) * 1990-05-30 1992-02-05 Daikin Ind Ltd Cooling medium
WO1993011201A1 (en) * 1991-12-03 1993-06-10 United States Environmental Protection Agency Refrigerant compositions and processes for using same

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0433989A (en) * 1990-05-30 1992-02-05 Daikin Ind Ltd Cooling medium
WO1993011201A1 (en) * 1991-12-03 1993-06-10 United States Environmental Protection Agency Refrigerant compositions and processes for using same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch Week 9212, Derwent World Patents Index; Class E16, AN 92-091756, XP002048669 *

Also Published As

Publication number Publication date
ES2167012T3 (en) 2002-05-01
AU3949697A (en) 1998-03-19
GB9618180D0 (en) 1996-10-09
DE69708123D1 (en) 2001-12-13
DE69708123T2 (en) 2002-06-06
JP2000516980A (en) 2000-12-19
EP0922075A1 (en) 1999-06-16
EP0922075B1 (en) 2001-11-07
ATE208412T1 (en) 2001-11-15

Similar Documents

Publication Publication Date Title
US6117356A (en) Refrigerant compositions
EP0770113B1 (en) Refrigerant compositions
US6106740A (en) Non-azeotropic refrigerant composition of CO2, R-125, R-143a and R-22
EP0772659A1 (en) Refrigerant compositions
EP0770112B1 (en) Refrigerant compositions
WO1997007179A1 (en) Refrigerant compositions
WO2008113984A1 (en) Refrigerant composition
EP0922077B1 (en) Refrigerant compositions
EP0922075B1 (en) Refrigerant compositions
WO1997007181A1 (en) Refrigerant compositions
WO1996003472A1 (en) Refrigerant compositions
WO1993014173A1 (en) Compositions useful as refrigerants
WO1996002605A1 (en) Refrigerant compositions
WO1996002603A1 (en) Refrigerant compositions
EP0845020A1 (en) Refrigerant compositions

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GE GH HU IL IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT UA UG US UZ VN YU ZW AM AZ BY KG KZ MD RU TJ TM

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH KE LS MW SD SZ UG ZW AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
ENP Entry into the national phase

Ref country code: JP

Ref document number: 1998 511356

Kind code of ref document: A

Format of ref document f/p: F

WWE Wipo information: entry into national phase

Ref document number: 1997936797

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 1997936797

Country of ref document: EP

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWE Wipo information: entry into national phase

Ref document number: 09242808

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: CA

WWG Wipo information: grant in national office

Ref document number: 1997936797

Country of ref document: EP