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US3085065A - Process of transferring heat - Google Patents

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US3085065A
US3085065A US42154A US4215460A US3085065A US 3085065 A US3085065 A US 3085065A US 42154 A US42154 A US 42154A US 4215460 A US4215460 A US 4215460A US 3085065 A US3085065 A US 3085065A
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dichlorodifluoromethane
azeotrope
vapor pressure
refrigerant
transferring heat
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US42154A
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Donovan E Kvalnes
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EIDP Inc
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EI Du Pont de Nemours and Co
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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
    • C09K2205/12Hydrocarbons
    • 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
    • C09K2205/32The mixture being azeotropic

Definitions

  • the capacity of any given refrigeration compressor is roughly proportional to the pressure of the gas at the suction side of the compressor. Since the compressor can handle a fixed volume of gas per unit of time, an increase in the suction pressure means an increase in the number of moles of gas put through the compressor in a given time. An increase in the number of moles means an increase in the total amount of heat required to vaporize the liquid in the evaporator, and an increase in the amount of heat that is removed from the refrigerated space. In general, other factors, such as variations in the latent heat of vaporization, play a relatively minor part in determining the change in capacity of a given refrigerating apparatus which will result from the substitution of one refrigerant for another.
  • azeotropic mixtures of pure materials as refrigerants is disclosed in U.S. Patent No. 2,101,993 and elsewhere in the art. Such mixtures have the advantage over other gas mixtures that the vapor composition of the azeotrope is the same as the liquid composition with which it is in equilibrium. With non-azeotropic mixtures, fractionation takes place during the refrigeration cycle, with consequent increase in condenser pressures and reduction in evaporator pressures and an overall loss of efiiciency. Azeotropic gas mixtures are not subject to this defect.
  • this invention comprises a novel azeotropic composition which consists of a mixture of about 72% by weight of dichlorodifluoromethane and about 28% by weight of 1,1,2,2-tetrafluoroethane, and the process for transferring heat which comprises evaporating, compressing and condensing said azeotropic mixture in a refrigeration cycle.
  • dichlorodifluoromethane and 1,1,2,2-tetrafluoroethane form an azeotrope having a boiling point of about 33.6 C. at 14.7 lbs/sq. in. absolute (p.s.i.a.).
  • Said azeotrope consists of about 68.5 mole percent or about 72.0% by weight of dichlorodifiuoromethane and about 31.5 mole percent or about 28.0% by weight of 1,1,2,2-tetrafiuoroethane.
  • Said azeotrope is a very desirable refrigerant. It has a normal boiling point about 3.8 C. below that of dichlorodifluoromethane, and is particularly valuable for use in a refrigeration system designed for dichlorodifluoromethane to provide about a 19.5% increase in the capacity of that refrigeration system.
  • the accompanying drawing shows the vapor pressure curve of the azeotropic mixture of this invention (the vapor pressure as a function of temperature), along with the vapor pressure curves of pure dichlorodifiuoromethane and pure 1,1,2,2-tetra.fluoroethane.
  • the vapor pressure curve of the azeotrope is a straight line above and parallel to the vapor pressure curve for dichlorodifiuorome-thane.
  • the vapor pressure curve also indicates the presence of the azeotrope, since the vapor pressure of a non-azeotropic mixture would be less than that of dichlorodifluoromethane.
  • the curve indicates that the azeotrope is not affected by changes in temperature, which is very important for refrigeration use. If the mixture ceased to be an azeotrope at some temperature, the vapor pressure curve would drop to a point somewhere between the curves of the two components.
  • Dichlorodifluoromethane has a normal boiling point of 29.8 C. and 1,l,2,2-tetrafluoroethane has a normal boiling point of -19.7 C.
  • dichlorodifiuoromethane and 10.1% by weight of l,l,2,2-tetrafiuoroethane was subjected to careful fractionation, there was obtained, as the lowest boiling material, the azeotrope boiling at -33.li0.5 C. containing 31.6 mole percent or 28.0 weight percent of 1,l,2,2-tetrafluoroethane (by vapor phase chromatography), the remainder being dichlorodifluoromethane.
  • the azeotrope continued to distill until the tetrafiuoroethane was exhausted from the mixture in the still, whereupon pure dichlorodifluoromethane distilled.
  • a mixture containing 50 mole percent of l,l,2,2-tetrafluor-oethane and 50 mole percent of dichlorodifluoromethane was also prepared and fractionally distilled. Again, the azeotrope distilled first and, when the dichlorodifiuoromethane was exhausted, pure tetrafiuoroethane distilled. The separation was very sharp. The composition of the azeotrope was again determined by a vapor phase chromatography and was found to be 315:0.4 mole percent or 28.0 weight percent of 1,1,2,2-tetrafluoroethane and 68.5 mole percent or 72.0 weight percent of dichlorodifluoromethane. Thus, the two approaches to the azeotrope duplicate themselves extremely well.
  • the increase in efiiciency is due to the increased vapor pressure.
  • the increase in efliciency was determined at 0 C. (32 F.) by dividing the diiierence in vapor pressure between the azeotrope (52.6 p.s.i.a.) and dichlorodifluoromethane (44 p.s.i.a.) by the pressure of dichlorodifluorornethane, giving 0.195 or 19.5%.
  • Dichlorodifluoromethane is a readily available refrigerant which is manufactured on a very large scale.
  • 1,1,2,2- tetrafluoroethane is a known compound which is readily prepared by several methods, e.g. from 1,1,2,2-tetrabromoethane or 1,1,2,2-tetrach1oroethane (acetylene tetrachloride) as disclosed by Henne et al. in.J.A.C.S., 58, 887 (1936), and by Cuculo et al.
  • Tetrafluoropropionaldehyde is readily available from the corresponding alcohol as disclosed by Brace in US. Patent 2,842,601, which alcohol is commercially available.
  • this invention provides a novel azeotropic composition which is useful as a refrigerant and is particularly valuable for use in place of dichlorodifluoromethane to give greater refrigerating capacity in refrigerating systems designed for use with dichlorodifluoromethane. Therefore, it is apparent that this invention constitutes a valuable advance in and contribution to the art.
  • the process for transferring heat in a refrigeration cycle which comprises evaporating, compressing and condensing in said cycle an azeotropic mixture of about 72% by weight of dichlorodifluoromethane and about 28% by weight of 1,1,2,2-tetrafluoroethane.

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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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

April 9, 1963 D. E. KVALNES PROCESS OF TRANSFERRING HEAT Filed July 11, 1960 PRESSURE, PSIA.
9. 52:55:: T 3- ET on 3 "EO o INVENTOR DONOVAN E. KVALN E5 WKMM ATTORNEY 3,085,065 PROCESS OF TRANSFERRING HEAT Donovan E. Kvalnes, Chadds Ford, Pa., assignor to E. I. du Pont de Nemours and Company, Wilmington, Del, a corporation of Delaware Filed July 11, 1960, Ser. No. 42,154 1 Claim. (Cl. 252-67) which is available in the various members of the series.
Difluorodichloromethane (13.1. 29.8 C.), fluorotrichloromethane (B.P. 23.7 C.), fluorodichloromethane (B.P. 8.9 C.), monochlorodiiluoromethane (B.P -40.8 C.), and tetrafluorodichloroethane (B.P. 3.5 C.) are among the most commonly used compounds of this type When apparatus designed to employ a particular refrigerant has been installed, the need sometimes arises for greater refrigerating capacity. This may be obtained by the use of a refrigerant having a lower boiling point and consequently a higher vapor pressure at the temperature attained by the gas prior to its being compressed and liquefied. The capacity of any given refrigeration compressor is roughly proportional to the pressure of the gas at the suction side of the compressor. Since the compressor can handle a fixed volume of gas per unit of time, an increase in the suction pressure means an increase in the number of moles of gas put through the compressor in a given time. An increase in the number of moles means an increase in the total amount of heat required to vaporize the liquid in the evaporator, and an increase in the amount of heat that is removed from the refrigerated space. In general, other factors, such as variations in the latent heat of vaporization, play a relatively minor part in determining the change in capacity of a given refrigerating apparatus which will result from the substitution of one refrigerant for another.
In a given apparatus, it is not possible to use a refrigerant having a boiling point too much lower than that for which the apparatus has been designed, as the power input becomes undesirably high and the compressor motor becomes overloaded. In order to provide greater refrigerating capacity for installations designed for the use of dichlorodifluoromethane, it is therefore desirable to employ a gas which may be liquefied a few degrees below the boiling point of that material.
The use of azeotropic mixtures of pure materials as refrigerants is disclosed in U.S. Patent No. 2,101,993 and elsewhere in the art. Such mixtures have the advantage over other gas mixtures that the vapor composition of the azeotrope is the same as the liquid composition with which it is in equilibrium. With non-azeotropic mixtures, fractionation takes place during the refrigeration cycle, with consequent increase in condenser pressures and reduction in evaporator pressures and an overall loss of efiiciency. Azeotropic gas mixtures are not subject to this defect.
US. Patent 2,479,259 and Reissue Patent 23,358 disclose that dichlorodifluoromethane and 1,1-difluoroethane form an azeotrope which is a useful refrigerant. It is impossible to predict that an azeotrope will form between any two compounds and so it is impossible to pick any two refrigerants and combine them to obtain an azeotrope boiling at some particular point by prediction. If an azeotrope occurs at all, its boiling point is a function of the system and is not under the control of the experimenter. The
3,085,065 Patented Apr. 9, 1963 ice mere existence of a large number of fluorinated hydrocarbons does not aid in predicting the formation of azeotropes by mixtures thereof.
It is an object of this invention to provide a novel azeotropic composition. Another object is to provide an azeotropic composition which is low boiling and which is effective to provide greater refrigerating capacity with apparatus designed for use with dichlorodifluoromethane. A further object is to provide an improved process of refrigeration by evaporating, compressing and condensing said novel azeotropic mixture in a refrigeration cycle. Other objects are to provide new compositions of matter and to advance the art. Still other objects will appear hereinafter.
The above and other objects may be accomplished according to this invention which comprises a novel azeotropic composition which consists of a mixture of about 72% by weight of dichlorodifluoromethane and about 28% by weight of 1,1,2,2-tetrafluoroethane, and the process for transferring heat which comprises evaporating, compressing and condensing said azeotropic mixture in a refrigeration cycle.
It has been found that dichlorodifluoromethane and 1,1,2,2-tetrafluoroethane form an azeotrope having a boiling point of about 33.6 C. at 14.7 lbs/sq. in. absolute (p.s.i.a.). Said azeotrope consists of about 68.5 mole percent or about 72.0% by weight of dichlorodifiuoromethane and about 31.5 mole percent or about 28.0% by weight of 1,1,2,2-tetrafiuoroethane. Said azeotrope is a very desirable refrigerant. It has a normal boiling point about 3.8 C. below that of dichlorodifluoromethane, and is particularly valuable for use in a refrigeration system designed for dichlorodifluoromethane to provide about a 19.5% increase in the capacity of that refrigeration system.
The accompanying drawing shows the vapor pressure curve of the azeotropic mixture of this invention (the vapor pressure as a function of temperature), along with the vapor pressure curves of pure dichlorodifiuoromethane and pure 1,1,2,2-tetra.fluoroethane. It will be noted that the vapor pressure curve of the azeotrope is a straight line above and parallel to the vapor pressure curve for dichlorodifiuorome-thane. The vapor pressure curve also indicates the presence of the azeotrope, since the vapor pressure of a non-azeotropic mixture would be less than that of dichlorodifluoromethane. Furthermore, the curve indicates that the azeotrope is not affected by changes in temperature, which is very important for refrigeration use. If the mixture ceased to be an azeotrope at some temperature, the vapor pressure curve would drop to a point somewhere between the curves of the two components.
Dichlorodifluoromethane has a normal boiling point of 29.8 C. and 1,l,2,2-tetrafluoroethane has a normal boiling point of -19.7 C. When a mixture containing 89.9% by weight of dichlorodifiuoromethane and 10.1% by weight of l,l,2,2-tetrafiuoroethane was subjected to careful fractionation, there was obtained, as the lowest boiling material, the azeotrope boiling at -33.li0.5 C. containing 31.6 mole percent or 28.0 weight percent of 1,l,2,2-tetrafluoroethane (by vapor phase chromatography), the remainder being dichlorodifluoromethane. The azeotrope continued to distill until the tetrafiuoroethane was exhausted from the mixture in the still, whereupon pure dichlorodifluoromethane distilled.
A mixture containing 50 mole percent of l,l,2,2-tetrafluor-oethane and 50 mole percent of dichlorodifluoromethane was also prepared and fractionally distilled. Again, the azeotrope distilled first and, when the dichlorodifiuoromethane was exhausted, pure tetrafiuoroethane distilled. The separation was very sharp. The composition of the azeotrope was again determined by a vapor phase chromatography and was found to be 315:0.4 mole percent or 28.0 weight percent of 1,1,2,2-tetrafluoroethane and 68.5 mole percent or 72.0 weight percent of dichlorodifluoromethane. Thus, the two approaches to the azeotrope duplicate themselves extremely well.
The increase in efiiciency, obtained by substituting one refrigerant for another, is due to the increased vapor pressure. In the present case, the increase in efliciency was determined at 0 C. (32 F.) by dividing the diiierence in vapor pressure between the azeotrope (52.6 p.s.i.a.) and dichlorodifluoromethane (44 p.s.i.a.) by the pressure of dichlorodifluorornethane, giving 0.195 or 19.5%.
Dichlorodifluoromethane is a readily available refrigerant which is manufactured on a very large scale. 1,1,2,2- tetrafluoroethane is a known compound which is readily prepared by several methods, e.g. from 1,1,2,2-tetrabromoethane or 1,1,2,2-tetrach1oroethane (acetylene tetrachloride) as disclosed by Henne et al. in.J.A.C.S., 58, 887 (1936), and by Cuculo et al. in J.A.C.S, 74, 710 (1952), or from 2,2,3,3-tetrafluoropropionaldehyde by decarhonylation in the presence of alkali. Tetrafluoropropionaldehyde is readily available from the corresponding alcohol as disclosed by Brace in US. Patent 2,842,601, which alcohol is commercially available.
From the preceding description, it will be apparent that this invention provides a novel azeotropic composition which is useful as a refrigerant and is particularly valuable for use in place of dichlorodifluoromethane to give greater refrigerating capacity in refrigerating systems designed for use with dichlorodifluoromethane. Therefore, it is apparent that this invention constitutes a valuable advance in and contribution to the art.
The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
The process for transferring heat in a refrigeration cycle which comprises evaporating, compressing and condensing in said cycle an azeotropic mixture of about 72% by weight of dichlorodifluoromethane and about 28% by weight of 1,1,2,2-tetrafluoroethane.
References Cited in the file of this patent UNITED STATES PATENTS 2,479,259 Reed et a1 Aug. 16, 1949 2,615,926 Benning et al. Oct. 28, 1952 2,912,383 Huth Nov. 10, 1959
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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3530073A (en) * 1968-09-30 1970-09-22 Union Carbide Corp Azeotropic composition
US4155865A (en) * 1977-12-27 1979-05-22 Allied Chemical Corporation Constant boiling mixtures of 1,1,2,2-tetrafluoroethane and 1,1,1,2-tetrafluorochloroethane
EP0030127A1 (en) * 1979-11-30 1981-06-10 Daikin Kogyo Co., Ltd. Absorption refrigerant compositions for use in absorption refrigeration systems
WO1991005027A1 (en) * 1989-09-26 1991-04-18 Allied-Signal Inc. Azeotrope-like compositions of pentafluoroethane and difluoromethane
US5492647A (en) * 1995-05-08 1996-02-20 Dow Corning Corporation Octamethylcyclotetrasiloxane azeotropes
EP0739998A2 (en) 1995-04-24 1996-10-30 Dow Corning Corporation Azeotropes of octamethyltrisiloxane and aliphatic or alicyclic alcohols
US5834416A (en) * 1997-08-19 1998-11-10 Dow Corning Corporation Azeotropes of alkyl esters and hexamethyldisiloxane
US6846850B2 (en) 2003-01-22 2005-01-25 Bayer Materialscience Llc Rigid polyurethane foams with improved properties
US20070069175A1 (en) * 2002-10-25 2007-03-29 Honeywell International, Inc. Fluorinated alkene refrigerant compositions
US20090092556A1 (en) * 2004-04-16 2009-04-09 Honeywell International Inc. Azeotrope-like compositions of difluoromethane and trifluoroiodomethane
US20090278076A1 (en) * 2002-10-25 2009-11-12 Honeywell International, Inc. Compositions Containing Fluorine Substituted Olefins
US20090302285A1 (en) * 2002-10-25 2009-12-10 Honeywell International, Inc. Compositions and methods containing fluorine substituted olefins
US20100127209A1 (en) * 2004-04-29 2010-05-27 Honeywell International Inc. Compositions Comprising Tetrafluoropropene And Carbon Dioxide
US20100155652A1 (en) * 2006-03-10 2010-06-24 Honeywell International Inc. Method for generating pollution credits
US8790539B2 (en) 2008-03-07 2014-07-29 Arkema Inc. Azeotrope-like composition of 1,1,1,2,2,3,3-heptafluoro-3-methoxypropane and 1-chloro-3,3,3-trifluoropropene

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2479259A (en) * 1946-05-10 1949-08-16 Carrier Corp Process for producing increased refrigeration
US2615926A (en) * 1949-03-09 1952-10-28 Du Pont Process for preparing organic compounds containing fluorine
US2912383A (en) * 1956-06-01 1959-11-10 Sun Oil Co Compression refrigeration working fluid

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2479259A (en) * 1946-05-10 1949-08-16 Carrier Corp Process for producing increased refrigeration
US2615926A (en) * 1949-03-09 1952-10-28 Du Pont Process for preparing organic compounds containing fluorine
US2912383A (en) * 1956-06-01 1959-11-10 Sun Oil Co Compression refrigeration working fluid

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3530073A (en) * 1968-09-30 1970-09-22 Union Carbide Corp Azeotropic composition
US4155865A (en) * 1977-12-27 1979-05-22 Allied Chemical Corporation Constant boiling mixtures of 1,1,2,2-tetrafluoroethane and 1,1,1,2-tetrafluorochloroethane
EP0030127A1 (en) * 1979-11-30 1981-06-10 Daikin Kogyo Co., Ltd. Absorption refrigerant compositions for use in absorption refrigeration systems
US4428854A (en) 1979-11-30 1984-01-31 Daikin Kogyo Co., Ltd. Absorption refrigerant compositions for use in absorption refrigeration systems
WO1991005027A1 (en) * 1989-09-26 1991-04-18 Allied-Signal Inc. Azeotrope-like compositions of pentafluoroethane and difluoromethane
EP0739998A2 (en) 1995-04-24 1996-10-30 Dow Corning Corporation Azeotropes of octamethyltrisiloxane and aliphatic or alicyclic alcohols
EP0739998A3 (en) * 1995-04-24 1997-03-05 Dow Corning Azeotropes of octamethyltrisiloxane and aliphatic or alicyclic alcohols
US5492647A (en) * 1995-05-08 1996-02-20 Dow Corning Corporation Octamethylcyclotetrasiloxane azeotropes
EP0742292A2 (en) 1995-05-08 1996-11-13 Dow Corning Corporation Octamethylcyclotetrasiloxane azeotropes
EP0742292A3 (en) * 1995-05-08 1997-03-05 Dow Corning Octamethylcyclotetrasiloxane azeotropes
US5834416A (en) * 1997-08-19 1998-11-10 Dow Corning Corporation Azeotropes of alkyl esters and hexamethyldisiloxane
US20070069175A1 (en) * 2002-10-25 2007-03-29 Honeywell International, Inc. Fluorinated alkene refrigerant compositions
US8033120B2 (en) 2002-10-25 2011-10-11 Honeywell International Inc. Compositions and methods containing fluorine substituted olefins
US9631129B2 (en) 2002-10-25 2017-04-25 Honeywell International Inc. Fluorinated alkene refrigerant compositions
US20090278076A1 (en) * 2002-10-25 2009-11-12 Honeywell International, Inc. Compositions Containing Fluorine Substituted Olefins
US20090302285A1 (en) * 2002-10-25 2009-12-10 Honeywell International, Inc. Compositions and methods containing fluorine substituted olefins
US8065882B2 (en) 2002-10-25 2011-11-29 Honeywell International Inc. Compositions containing fluorine substituted olefins
US6846850B2 (en) 2003-01-22 2005-01-25 Bayer Materialscience Llc Rigid polyurethane foams with improved properties
US8163689B2 (en) 2004-04-16 2012-04-24 Honeywell International Inc. Azeotrope-like compositions of difluoromethane and trifluoroiodomethane
US8492327B2 (en) 2004-04-16 2013-07-23 Honeywell International Inc. Azeotrope-like compositions of difluoromethane and trifluoroiodomethane
US20090092556A1 (en) * 2004-04-16 2009-04-09 Honeywell International Inc. Azeotrope-like compositions of difluoromethane and trifluoroiodomethane
US8053404B2 (en) 2004-04-29 2011-11-08 Honeywell International Inc. Compositions comprising tetrafluoropropene and carbon dioxide
US20100127209A1 (en) * 2004-04-29 2010-05-27 Honeywell International Inc. Compositions Comprising Tetrafluoropropene And Carbon Dioxide
US20100155652A1 (en) * 2006-03-10 2010-06-24 Honeywell International Inc. Method for generating pollution credits
US8790539B2 (en) 2008-03-07 2014-07-29 Arkema Inc. Azeotrope-like composition of 1,1,1,2,2,3,3-heptafluoro-3-methoxypropane and 1-chloro-3,3,3-trifluoropropene

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