EP0620839A1 - Zusammensetzungen geeignet als kältemittel - Google Patents

Zusammensetzungen geeignet als kältemittel

Info

Publication number
EP0620839A1
EP0620839A1 EP93900354A EP93900354A EP0620839A1 EP 0620839 A1 EP0620839 A1 EP 0620839A1 EP 93900354 A EP93900354 A EP 93900354A EP 93900354 A EP93900354 A EP 93900354A EP 0620839 A1 EP0620839 A1 EP 0620839A1
Authority
EP
European Patent Office
Prior art keywords
trifluoromethyl ether
difluoromethyl
refrigerant
weight
ether
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP93900354A
Other languages
English (en)
French (fr)
Inventor
Richard Llewellyn Powell
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
Priority claimed from GB929200522A external-priority patent/GB9200522D0/en
Priority claimed from GB929200481A external-priority patent/GB9200481D0/en
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of EP0620839A1 publication Critical patent/EP0620839A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/02Materials undergoing a change of physical state when used
    • C09K5/04Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
    • C09K5/041Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
    • C09K5/044Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
    • C09K5/045Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds containing only fluorine as halogen
    • CCHEMISTRY; METALLURGY
    • 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
    • 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
    • C09K2205/11Ethers
    • C09K2205/112Halogenated ethers
    • 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

Definitions

  • the present invention is concerned with refrigerant compositions which are designed to replace dichlorodifluoromethane. (Refrigerant R-12) and the azeotropic mixture of
  • the mechanical energy required for compressing the vapour and pumping the liquid may be provided by an electric motor or an
  • the properties preferred of a refrigerant include low toxicity, non- flammability, non-corrosivity, high stability and 30 freedom from ob ectionable odour.
  • the present invention provides a refrigerant composition which may be used in place of Refrigerants R-12 and R-500, particularly the former.
  • the composition contains refrigerant compounds which have essentially zero ozone depletion potentials and comparatively low direct global warming potentials.
  • the present invention provides a refrigerant composition
  • a refrigerant composition comprising a mixture of difluoromethyl trifluoromethyl ether (CF3OCHF2) and at least one other fluorine containing compound selected from 1 , 1, 1 ,2-tetrafluoroethane (CF3CH2F), fluoromethyl trifluoromethyl ether (CF3OCH2F) and bis (difluoromethyl) ether (CHF2OCHF2) .
  • Refrigerant compositions in accordance with the present invention typically contain from 5 to 952 by weight of difluoromethyl trifluoromethyl ether and from 95 to 52 by weight of at least one compound selected from 1 ,1,1,2-tetrafluoroethane , fluoromethyl trifluoromethyl ether and bis (difluoromethyl ) ether.
  • the refrigerant compositions of the invention may contain other refrigerant compounds which have low and preferably zero ozone depletion potentials, for example other hydrofluoroalkanes and/or other fluorinated ethers containing residual hydrogen atoms. Examples of other hydrofluoroalkanes which may be incorporated in the refrigerant compositions of the invention include difluoromethane (R-32), 1, 1,1-trifluoroethane (R-143a),
  • fluorinated ethers 1, 1,2,2-tetrafluoroethane (R-134), pentafluoroethane (R-125) and 1,1-difluoroethane (R-152a).
  • fluorinated ethers which may be included in the refrigerant compositions of the invention are the fluorinated dimethyl ethers containing residual hydrogen atoms.
  • the refrigerant compositions of the invention may comprise other refrigerant compounds
  • the preferred refrigerant compositions of the invention consist essentially of difluoromethyl trifluoromethyl ether and at least one other fluorine containing compound selected from 1,1 , 1 ,2-tetrafluoroethane , fluoromethyl trifluoromethyl ether and bis (difluoromethyl) ether.
  • the refrigerant compositions of the invention may be zeotropic they are preferably azeotropic or azeotrope-like.
  • the preferred compounds for use in admixture with the difluoromethyl trifluoromethyl ether are 1,1, 1,2-tetrafluoroethane and fluoromethyl trifluoromethyl ether, since the resulting refrigerant compositions may provide a particularly suitable replacement for Refrigerant R-12.
  • a refrigerant composition comprising a mixture of difluoromethyl trifluoromethyl ether and 1,1,1,2-tetrafluoroethane .
  • Such compositions may additionally comprise one or more further refrigerant compounds, such as fluoromethyl trifluoromethyl ether and/or bis (difluoromethyl ) ether and/or at least one other fluorinated ether containing residual hydrogen atoms and/or at least one other hydrofluoroalkane .
  • refrigerant compositions which consist essentially of difluoromethyl trifluoromethyl ether and 1,1,1, 2-tetrafluoroethane are preferred.
  • compositions comprising difluoromethyl trifluoromethyl ether and 1,1,1,2-tetrafluoroethane as essential components
  • compositions comprising from 25 to 75 2 by weight of di luoromethyl trifluoromethyl ether and from 75 to 25 2 by weight of 1 ,1,1,2-tetrafluoroethane are preferred, with compositions comprising from 25 to 50 2 by weight of difluoromethyl trifluoromethyl ether and from 75 to 50 2 by weight of 1,1,1,2-tetrafluoroethane being especially preferred.
  • Table 1 shows the results of analysing the performance of a number of refrigerant compositions of the invention in a refrigeration cycle to assess the suitability thereof as a replacement for R-12. All the compositions analysed comprised difluoromethyl trifluoromethyl ether (E-125 in the Table) and 1 ,1 , 1 ,2-tetrafluoroethane (R-134a in the Table) in varying amounts. The percentage by weight of each component in the refrigerant compositions analysed is" given in the second row of the Table. Thus, the results of analysing the performance of the following refrigerant compositions are given in Table 1:
  • a composition comprising 75 2 by weight of
  • 1,1,1,2-tetrafluoroethane and 50 2 by weight of difluoromethyl trifluoromethyl ether are 1,1,1,2-tetrafluoroethane and 50 2 by weight of difluoromethyl trifluoromethyl ether.
  • Isentropic Compressor Efficiency 75 2
  • refrigerant compositions according to the invention comprising difluoromethyl trifluoromethyl ether and 1,1,1,2-tetrafluoroethane can exhibit a performance in a refrigeration system which is comparable to that of Refrigerant R-12. It is also apparent that refrigerant compositions containing from 25 to 50 2 by weight of difluoromethyl trifluoromethyl ether and from 75 to 50 2 by weight of 1,1,1,2-tetrafluoroethane offer a particularly suitable alternative to Refrigerant R-12. Furthermore, the glide in the evaporator for all the mixed refrigerant compositions tested was 0.8°C or less showing that such compositions are azeotrope like.
  • a refrigerant composition comprising a mixture of difluoromethyl trifluoromethyl ether and fluoromethyl trifluoromethyl ether.
  • Such compositions may additionally comprise one or more further refrigerant compounds, such as 1 ,1, 1 ,2-tetrafluoroethane and/or bis (difluoromethyl ) ether and/or at least one other fluorinated ether containing residual hydrogen atoms and/or at least one other hydrofluoroalkane .
  • refrigerant compositions which consist essentially of difluoromethyl trifluoromethyl ether and fluoromethyl trifluoromethyl ether are preferred.
  • compositions comprising difluoromethyl trifluoromethyl ether and fluoromethyl trifluoromethyl ether benefit from the high capacity (cooling duty per unit swept volume) of the former compound and high efficiency (coefficient of performance) of the latter compound.
  • Such compositions preferably comprise from 25 to 75 2 by weight of difluoromethyl trifluoromethyl ether and from 75 to 25 2 by weight of fluoromethyl trifluoromethyl ether.
  • Table 2 shows the results of analysing the performance of a number of refrigerant compositions of the invention in a refrigeration cycle to assess the suitability thereof as a replacement for R-12. All the compositions analysed comprised difluoromethyl trifluoromethyl ether (E-125 in the Table) and fluoromethyl trifluoromethyl ether (E-134a in the Table) in varying amounts. The percentage by weight of each component in the refrigerant compositions analysed is given in the second row of the Table. Thus, the results of analysing the performance of the following refrigerant compositions are given in Table 2:
  • a composition comprising 75 2 by weight of difluoromethyl trifluoromethyl ether and 25 2 by weight of fluoromethyl trifluoromethyl ether.
  • a composition comprising 50 2 by weight of difluoromethyl trifluoromethyl ether and 50 2 by weight of fluoromethyl trifluoromethyl ether.
  • a composition comprising 25 2 by weight of difluoromethyl trifluoromethyl ether and 75 2 by weight of fluoromethyl trifluoromethyl ether.
  • refrigerant compositions according to the invention comprising difluoromethyl trifluoromethyl ether and fluoromethyl trifluoromethyl ether can exhibit a performance in a refrigeration system which is not too far removed from that of Refrigerant R-12. Furthermore, the glide in the evaporator for all the mixed refrigerant compositions tested was 1.9°C or less showing that such compositions are azeotrope like.
  • the refrigerant compositions of the invention may be prepared by a simple mixing process.
  • compositions are useful in all types of compression cycle heat transfer devices. Thus, they may be used to provide cooling by a method involving condensing the refrigerant composition and thereafter evaporating it in a heat exchange relationship with a- body to be cooled. They may also be used to provide heating by a method involving condensing the refrigerant composition in a heat exchange relationship with a body to be heated and thereafter evaporating it.
  • compositions of the invention provide a good compromise between atmospheric lifetime, ozone depletion potential and efficiency. They are especially valuable for applications currently satisfied by R-12 such as domestic refrigeration.

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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Lubricants (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
EP93900354A 1992-01-10 1992-12-23 Zusammensetzungen geeignet als kältemittel Withdrawn EP0620839A1 (de)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
GB929200522A GB9200522D0 (en) 1992-01-10 1992-01-10 Compositions useful as refrigerants
GB9200522 1992-01-10
GB929200481A GB9200481D0 (en) 1992-01-10 1992-01-10 Compositions useful as refrigerants
GB9200481 1992-01-10
PCT/GB1992/002384 WO1993014175A1 (en) 1992-01-10 1992-12-23 Compositions useful as refrigerants

Publications (1)

Publication Number Publication Date
EP0620839A1 true EP0620839A1 (de) 1994-10-26

Family

ID=26300143

Family Applications (1)

Application Number Title Priority Date Filing Date
EP93900354A Withdrawn EP0620839A1 (de) 1992-01-10 1992-12-23 Zusammensetzungen geeignet als kältemittel

Country Status (7)

Country Link
EP (1) EP0620839A1 (de)
JP (1) JPH07502775A (de)
KR (1) KR940703901A (de)
AU (1) AU668120B2 (de)
BR (1) BR9207027A (de)
CA (1) CA2126186A1 (de)
WO (1) WO1993014175A1 (de)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2125143A1 (en) * 1991-12-03 1993-06-10 Cynthia L. Gage Refrigerant compositions and processes for using same
GB9200523D0 (en) * 1992-01-10 1992-02-26 Ici Plc Compositions useful as refrigerants
GB9200521D0 (en) * 1992-01-10 1992-02-26 Ici Plc Compositions useful as refrigerants
US5605882A (en) 1992-05-28 1997-02-25 E. I. Du Pont De Nemours And Company Azeotrope(like) compositions of pentafluorodimethyl ether and difluoromethane
TW305874B (de) * 1992-10-14 1997-05-21 Du Pont
US5484546A (en) * 1993-05-19 1996-01-16 E. I. Du Pont De Nemours And Company Refrigerant compositions including an acylic fluoroether
FR2732242B1 (fr) * 1995-03-28 1997-05-23 Elf Aquitaine Composite actif a structure feuilletee et son utilisation comme milieu reactionnel
FR2733241B1 (fr) * 1995-04-20 1997-05-30 Atochem Elf Sa Melanges pseudo-azeotropiques a base de difluoromethane et de pentafluorodimethylether , et leurs applications comme fluides frigorigenes
WO1997014764A1 (en) * 1995-10-18 1997-04-24 Alliedsignal Inc. Compositions of pentafluoromethyl ether and a hydrocarbon
US20100025619A1 (en) * 2006-07-12 2010-02-04 Solvay Fluor Gmbh Method for heating and cooling using fluoroether compounds, compositions suitable therefore and their use
TW201413192A (zh) * 2012-08-01 2014-04-01 Du Pont E-1,1,1,4,4,4-六氟-2-丁烯在熱泵的使用

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4961321A (en) * 1989-02-28 1990-10-09 W. R. Grace & Co.-Conn. Bis (difluoromethyl) ether refrigerant
CA2077910C (en) * 1990-03-12 2003-10-21 Philip L. Bartlett Azeotropic composition of 1,1,1,2-tetrafluoroethane and dimethyl ether
CA2125143A1 (en) * 1991-12-03 1993-06-10 Cynthia L. Gage Refrigerant compositions and processes for using same
GB9200523D0 (en) * 1992-01-10 1992-02-26 Ici Plc Compositions useful as refrigerants
GB9200521D0 (en) * 1992-01-10 1992-02-26 Ici Plc Compositions useful as refrigerants

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9314175A1 *

Also Published As

Publication number Publication date
WO1993014175A1 (en) 1993-07-22
CA2126186A1 (en) 1993-07-22
KR940703901A (ko) 1994-12-12
AU3168993A (en) 1993-08-03
AU668120B2 (en) 1996-04-26
JPH07502775A (ja) 1995-03-23
BR9207027A (pt) 1995-12-05

Similar Documents

Publication Publication Date Title
EP0509673B2 (de) Kühlzusammensetzungen
US6117356A (en) Refrigerant compositions
WO2008009922A2 (en) Heat transfer compositions
EP0845022A1 (de) Kühlmittelzusammensetzungen
EP0620838A1 (de) Zusammensetzungen geeignet als kaeltemittel
EP0620839A1 (de) Zusammensetzungen geeignet als kältemittel
EP0770113B1 (de) Kühlzusammensetzungen
WO1997007179A1 (en) Refrigerant compositions
EP0620837A1 (de) Zusammensetzungen geeignet als kaeltemittel
EP0770112B1 (de) Kühlmittelzusammensetzungen
EP0922077B1 (de) Kühlmittelzusammensetzungen
WO1997007181A1 (en) Refrigerant compositions
EP0922075B1 (de) Kühlmittelzusammensetzungen
EP0845020A1 (de) Kühlmittelzusammensetzungen
WO1996002605A1 (en) Refrigerant compositions
WO1996002603A1 (en) Refrigerant compositions

Legal Events

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

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19940608

AK Designated contracting states

Kind code of ref document: A1

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

17Q First examination report despatched

Effective date: 19941223

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

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

18D Application deemed to be withdrawn

Effective date: 19960825