CA2227910A1 - Refrigerant compositions - Google Patents

Refrigerant compositions Download PDF

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Publication number
CA2227910A1
CA2227910A1 CA 2227910 CA2227910A CA2227910A1 CA 2227910 A1 CA2227910 A1 CA 2227910A1 CA 2227910 CA2227910 CA 2227910 CA 2227910 A CA2227910 A CA 2227910A CA 2227910 A1 CA2227910 A1 CA 2227910A1
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CA
Canada
Prior art keywords
weight
refrigerant composition
refrigerant
azeotropic refrigerant
composition
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.)
Abandoned
Application number
CA 2227910
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
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Individual
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
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Publication of CA2227910A1 publication Critical patent/CA2227910A1/en
Abandoned legal-status Critical Current

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    • 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
    • C09K2205/10Components
    • C09K2205/106Carbon dioxide
    • 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
    • C09K2205/10Components
    • C09K2205/12Hydrocarbons
    • 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
    • C09K2205/10Components
    • C09K2205/12Hydrocarbons
    • C09K2205/122Halogenated hydrocarbons
    • 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

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  • 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)

Abstract

A non-azeotropic refrigerant composition is described comprising (A) carbon dioxide (CO2), (B) pentafluoroethane (R-125), (C) propane (R-290), and (D) chlorodifluoromethane (R-22).

Description

CA 022279l0 l998-0l-26 1 REFRIGE~ANT COMPOSITIONS

i,~ The present invention relates to non-azeotropic refrigerant compositions and more particularly to non-azeotropic refrigerant compositions which can be used in the low temperature refrigeration applications currently satisfied by refrigerant R-502 which is an azeotropic mixture of chlorodifluoromethane (refrigerant R-22) and chloropentafluoroethane (refrigerant R-115).
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 surrounding 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 trichlorofluoromethane (refrigerant R-ll), dichlorodifluoromethane (refrigerant R-12), chlorodifluoromethane (refrigerant R-ZZ) and the azeotropic mixture of chlorodifluoromethane and chloropentafluoroethane (refrigerant R-115); the azeotrope being refrigerant R-50Z. Refrigerant R-50Z, for example, has been widely used in low temperature refrigeration applications.

CA 022279l0 l998-0l-26 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 hydrofluoroalk~nes, 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-502.
Furthermore, very real benefits could be realised by a new replacement refrigerant having a higher refrigeration capacity than the replacement refrigerants known in the art.

The present invention provides a non-azeotropic refrigerant composition comprising a mixture of compounds having low or zero ozone depletion potentials which can be used in the low temperature refrigeration applications currently satisfied by refrigerant R-502.
The non-azeotropic refrigerant composition of the invention can exhibit an advantageously high refrigeration capacity.
According to the present invention there is provided a non-azeotropic (zeotropic) refrigerant composition comprising:
(A) carbon dioxide (C02);
(B) pentafluoroethane (R-125);
(C) propane (R-290); and (D) chlorodifluoromethane (R-22).
The zeotropic refrigerant composition of the invention comprises four separate components.
The first component (component (A)) is carbon dioxide (C02) which exhibits a low temperature refrigeration action subliming at around -78.5~C. The second component (component (B)) is pentafluoroethane (R-125) which has a boiling point of around -48.5~C. The third component (component (C)) is propane (R-290) which has a boiling point of around -42.1~C. The fourth component (component (D)) is chlorodifluoromethane (R-2Z) which has a boiling point of around -40.8~C.
The amounts of the various components in the refrigerant composition may be varied within wide limits, but typically the refrigerant composition will comprise from 1 to 20 Z by weight C02, from Z5 to 70 Z by weight R-125, from 0.5 to 15 Z by weight R-Z90 and from 25 to 70 Z by weight R-22.
A preferred refrigerant composition of the invention in terms of its suitability as a replacement for refrigerant R-502 is one comprising from 1 to 15 Z by weight C02, from 30 to 65 Z by weight R-125, from 0.5 to 10 % by weight R-290 and from 30 to 65 Z by weight R-22.

CA 022279l0 l998-0l-26 A particularly preferred refrigerant composition of the invention in terms of its suitability as a replacement for refrigerant R-50Z is one comprising from 1 to 15 % by weight, more particularly from Z to 10 % by weight, C02, from 50 to 65 % by weight. more particularly from 50 to 60 % by weight, R-125, from 0.5 to 10 % by weight, more particularly from l to 5 Z by weight, R-290 and from 30 to 45 Z by weight, more particularly from 30 to 40 Z by weight, R-Z2. An especially preferred refrigerant composition of the invention is one comprising from 2 to 5 Z by weight C02, from 55 to 60 Z by weight R-125, from 1 to 3 Z by weight R-290 and from 35 to 40 Z by weight R-22.
Another particularly preferred refrigerant composition of the invention in terms of its suitability as a replacement for refrigerant R-50Z is one comprising from 1 to 15 Z by weight. more particularLy from 2 to 10 Z by weight, C02, from 30 to 45 % by weight, more particularly from 30 to 40 % by weight, R-lZ5, from 0.5 to lO Z by weight, more particularly from 1 to 5 Z by weight, R-Z90 and from 50 to 65 Z by weight, more particularly from 50 to 60 Z by weight, R-Z2. An especially preferred refrigerant composition of the invention is one comprising from 2 to 5 % by weight C02, from 35 to 40 Z by weight R-125, from 1 to 3 % by weight R-290 and from 55 to 60 Z by weight R-22.
The refrigerant composition of the invention may 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 CA 02227910 l99X-01-26 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. Usually, 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.
It may also be possible to use inexpensive lubricants based on mineral oils or alkyl benzenes with the refrigerant composition of the invention since the propane contained in the composition may allow it to successfully transport a mineral oil or alkyl benzene type lubricant around a refrigeration circuit and return it to the compressor. Oil return of mineral oil or alkyl benzene lubricants may be further assisted by adding pentane to the refrigerant composition.
When pentane is added, it will preferably be present in an amount of from l to l0 Z by weight on the total weight of the refrigerant composition.
The zeotropic refrigerant composition of the present invention may be used to provide the desired cooling in heat transfer devices such as low temperature refrigeration systems by a method which involves condensing the refrigerant composition and thereafter ~ .

evaporating it in a heat e~h~nge relationship with a heat transfer fluid to be cooled. In particular, the refrigerant composition of the invention may be employed as a replacement for refrigerant R-502 in low temperature refrigeration applications.
The present invention is now illustrated but not limited with reference to the following example.
-CA 022279l0 l998-0l-26 l Example 1 The performance of six refrigerant compositions of the invention in a low temperature refrigeration cycle was investigated using standard refrigeration cycle analysis techniques in order to assess the suitability thereof as a replacement for R-50Z. The following refrigerant compositions were subjected to the cycle analysis:

(l) A composition comprising 2 Z by weight C0z, 58.8 Z by weight R-125, Z Z by weight R-290 and 37.Z Z by weight R-22.
(2) A composition comprising 5 Z by weight C02, 57 % by weight R-125, 1.9 Z by weight R-Z90 and 36.1 Z by weight R-22.
(3) A composition comprising 10 Z by weight C02, 54 Z by weight R-125, 1.8 2 by weight R-290 and 34.2 % by weight R-22.
(4) A composition comprising 2 % by weight C02, 37.2 Z by weight R-125, 2 Z by weight R-290 and 58.8 Z by weight R-22.
(5) A composition comprising 5 2 by weight C02, 36.1 Z by weight R-125, 1.9 % by weight R-290 and 57 Z by weight R-22.
(6) A composition comprising 10 Z by weight C02, 34.2 Z by weight R-125, 1.8 Z by weight R-290 and 54 Z by weight R-22.

The following operating conditions were used in the cycle analysis.

Mean Evaporator Temperature: -40~C
Mean Condenser Temperature: 40~C
Amount of Superheat: 10~C
Amount of Subcooling: 5~C
Isentropic Compressor Efficiency: 75 Z
Cooling Duty: 1 kW

The results of analysing the performance of the six refrigerant compositions in a low temperature refrigeration cycle using these operating conditions are given in Table 1.

The performance parameters of the refrigerant compositions which are presented in Table l, i.e. condenser pressure, evaporator , f 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 (refrigeration effect) achieved to mechanical energy supplied to the compressor), and the glides in the evaporator and condenser (the temperature range over which the re-frigerant composition boils in the evaporator and condenses in the condenser), are all art recognised parameters.
The performance of refrigerant R-502 under the same operating conditions is also shown in Table l by way of comparison.
It is apparent from Table l that the refrigerant compositions of the invention exhibited higher refrigeration capacities than refrigerant R-50Z and that the refrigeration capacity increased as the C02 content in the composition increased. It is also apparent from the results given in Table l that the performance of the refrigerant composition of the invention in a low temperature refrigeration cycle is such that it could make an acceptable replacement for refrigerant R-502.

CA 022279l0 l998-0l-26 W O 97/07180 PCTtGB96/01956 ~,.
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Claims (13)

Claims:
1. A non-azeotropic refrigerant composition comprising:
(A) carbon dioxide (CO2);
(B) pentafluoroethane (R-125);
(C) propane (R-290); and (D) chlorodifluoromethane (R-22).
2. A non-azeotropic refrigerant composition as claimed in claim 1 comprising from 1 to 20 % by weight CO2, from 25 to 70 % by weight R-125, from 0.5 to 15 % by weight R-290 and from 25 to 70 % by weight R-22.
3. A non-azeotropic refrigerant composition as claimed in claim 2 comprising from 1 to 15 % by weight CO2, from 30 to 65 % by weight R-125, from 0.5 to 10 % by weight R-290 and from 30 to 65 % by weight R-22.
4. A non-azeotropic refrigerant composition as claimed in claim 3 comprising from 1 to 15 % by weight CO2, from 50 to 65 % by weight R-125, from 0.5 to 10 % by weight R-290 and from 30 to 45 % by weight R-22.
5. A non-azeotropic refrigerant composition as claimed in claim 4 comprising from 2 to 10 % by weight CO2, from 50 to 60 % by weight R-125, from 1 to 5 % by weight R-290 and from 30 to 40 % by-weight, R-22.
6. A non-azeotropic refrigerant composition as claimed in claim 5 comprising from 2 to 5 % by weight CO2, from 55 to 60 % by weight R-125, from 1 to 3 % by weight R-290 and from 35 to 40 % by weight R-22.
7. A non-azeotropic refrigerant composition as claimed in claim 3 comprising from 1 to 15 % by weight CO2, from 30 to 45 % by weight R-125, from 0.5 to 10 % by weight R-290 and from 50 to 65 % by weight R-22.
8. A non-azeotropic refrigerant composition as claimed in claim 7 comprising from 2 to 10 % by weight CO2, from 30 to 40 % by weight R-125, from 1 to 5 % by weight R-290 and from 50 to 60 % by weight R-22.
9. A non-azeotropic refrigerant composition as claimed in claim 8 comprising from 2 to 5 % by weight CO2, from 35 to 40 % by weight R-125, from 1 to 3 % by weight R-290 and from 55 to 60 % by weight R-22.
10. A heat transfer device containing a non-azeotropic refrigerant composition as claimed in any one of claims 1 to 9.
11. A low temperature refrigeration system containing a non-azeotropic refrigerant composition as claimed in any one of claims 1 to 9.
12. A method for providing cooling which comprises condensing a non-azeotropic refrigerant composition as claimed in any one of claims 1 to 9 and thereafter evaporating it in a heat exchange relationship with a heat transfer fluid to be cooled.
13. The use of a non-azeotropic refrigerant composition as claimed in any one of claims 1 to 9 as a replacement for refrigerant R-502 in low temperature refrigeration applications.
CA 2227910 1995-08-18 1996-08-12 Refrigerant compositions Abandoned CA2227910A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9516919.9A GB9516919D0 (en) 1995-08-18 1995-08-18 Refrigerant compositions
GB9516919.9 1995-08-18

Publications (1)

Publication Number Publication Date
CA2227910A1 true CA2227910A1 (en) 1997-02-27

Family

ID=10779409

Family Applications (1)

Application Number Title Priority Date Filing Date
CA 2227910 Abandoned CA2227910A1 (en) 1995-08-18 1996-08-12 Refrigerant compositions

Country Status (6)

Country Link
EP (1) EP0845020A1 (en)
JP (1) JPH11511191A (en)
AU (1) AU6707796A (en)
CA (1) CA2227910A1 (en)
GB (1) GB9516919D0 (en)
WO (1) WO1997007180A1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004198063A (en) * 2002-12-20 2004-07-15 Sanyo Electric Co Ltd Non-azeotropic refrigerant mixture, refrigerating cycle and refrigerating device
JP2004198062A (en) * 2002-12-20 2004-07-15 Sanyo Electric Co Ltd Refrigerating device
US7861541B2 (en) 2004-07-13 2011-01-04 Tiax Llc System and method of refrigeration

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69126219T2 (en) * 1990-07-26 1997-12-11 Du Pont Quasi-azeotropic mixtures for use as refrigerants
DE4116274C2 (en) * 1991-05-17 1998-03-19 Forschungszentrum Fuer Kaeltet Refrigerant
US5360566A (en) * 1992-11-06 1994-11-01 Intermagnetics General Corporation Hydrocarbon refrigerant for closed cycle refrigerant systems
IT1270960B (en) * 1993-08-13 1997-05-26 Ausimont Spa ALMOST AZEOTROPIC TERNARY MIXTURES WITH REFRIGERANT FLUIDS

Also Published As

Publication number Publication date
JPH11511191A (en) 1999-09-28
GB9516919D0 (en) 1995-10-18
WO1997007180A1 (en) 1997-02-27
AU6707796A (en) 1997-03-12
EP0845020A1 (en) 1998-06-03

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