US3047506A - Refrigeration process - Google Patents
Refrigeration process Download PDFInfo
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- US3047506A US3047506A US702646A US70264657A US3047506A US 3047506 A US3047506 A US 3047506A US 702646 A US702646 A US 702646A US 70264657 A US70264657 A US 70264657A US 3047506 A US3047506 A US 3047506A
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- Prior art keywords
- ethyl chloride
- dichlorotetrafluoroethane
- mol percent
- mixture
- compositions
- Prior art date
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- 238000000034 method Methods 0.000 title claims description 6
- 238000005057 refrigeration Methods 0.000 title claims description 5
- 239000000203 mixture Substances 0.000 claims description 60
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 claims description 26
- 229960003750 ethyl chloride Drugs 0.000 claims description 25
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 claims description 19
- 229940087091 dichlorotetrafluoroethane Drugs 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 5
- 238000001704 evaporation Methods 0.000 claims description 4
- 238000009835 boiling Methods 0.000 description 17
- 239000003380 propellant Substances 0.000 description 12
- 239000003507 refrigerant Substances 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 239000000443 aerosol Substances 0.000 description 8
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 7
- 239000007788 liquid Substances 0.000 description 4
- BAMUEXIPKSRTBS-UHFFFAOYSA-N 1,1-dichloro-1,2,2,2-tetrafluoroethane Chemical class FC(F)(F)C(F)(Cl)Cl BAMUEXIPKSRTBS-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- BHNZEZWIUMJCGF-UHFFFAOYSA-N 1-chloro-1,1-difluoroethane Chemical compound CC(F)(F)Cl BHNZEZWIUMJCGF-UHFFFAOYSA-N 0.000 description 1
- GAXAVDBUPHBRCT-UHFFFAOYSA-N C(C)Cl.ClC(C(F)(F)F)(F)Cl Chemical compound C(C)Cl.ClC(C(F)(F)F)(F)Cl GAXAVDBUPHBRCT-UHFFFAOYSA-N 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 235000019606 astringent taste Nutrition 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-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
- C09K5/02—Materials undergoing a change of physical state when used
Definitions
- Dichlorotetrafiuoroethanes are commercially produced as mixtures of the two isomers, one representative mixture containing mainly the symmetrical isomer CClFgCClF with a few percent of the unsymmetrical isomer OCl FCF and another typical mixture containing mainly the unsymmetrical isomer with a few percent of the symmetrical isomer.
- the boiling points of the pure isomers are 3.64 C. and 3.14" C. for the symmetrical and unsymmetrical isomers respectively; the boiling points of commercial products being intermediate these limits.
- Objects of the invention include provision of dichlorotetrafluoroethane-ethyl chloride mixtures which boil at substantially constant temperature and function as a single substance. These mixtures are useful as refrigerants and as aerosol propellants. As refrigerants, such mixtures at lower cost afford increased pressure and greater refrigerating capacity with respect to refrigerating apparatus designed for use of dichlorotetrafluoroethane alone, and as aerosols such mixtures at lower cost provide increased pressure, and improved solubility for common aerosol ingredients.
- boiling point composition curve is very fiat and that mixtures containing ethyl chloride in the range of about 22-50 mol percent all boil between about 1.1 and 16 C., and that with regard to particular specific mixtures within the indicated 22-50 mol percent range, boiling points of such mixtures may vary only to the extent of about 0.2 C.
- compositions at or close to the 36-37 mol percent ethyl chloride content in order to avoid even minor differences in liquid and vapor composition.
- differences in liquid and vapor composition are of lesser consequence, hence the whole range of 22-50 mol percent ethyl chloride composition may be employed to advantage.
- compositions containing at least about 50 mol percent of dichlorotetrafluoroethane are preferred.
- compositions of the invention require no special procedures.
- the dichlorotetrafluoroethane and the ethyl chloride em ployed should be substantially pure, and contain no substances deleteriously affecting use either as refrigerants or aerosol propellants.
- the compositions of the invention are chemically nonreactive, non-inflammable and substantially non-toxic.
- compositions of the invention may be used as refrigerants in any cooling systems in which cooling is eifected by evaporation and expansion of liquid refrigerants such as domestic and commercial refrigerators, and domestic or commercial cooling or air-conditioning systems.
- cooling is eifected by evaporation and expansion of liquid refrigerants
- liquid refrigerants such as domestic and commercial refrigerators, and domestic or commercial cooling or air-conditioning systems.
- the expanded gas is compressed and condensed to a liquid and is recycled to the expansion stage.
- the products of the invention supply distinct advantages. Whereas commercial dichlorotetrafiuoroethanes boil in the range of 3.23.6 C. and have vapor pressures in the range of 27.6-28.1 p.-s.i.g. at 70 R, such pressures are not sufficient to propel the aerosol product to :give the desired fine particle size in the spray. Consequently it is usually necessary to mix dichlorotetrafluoroethane with another higher pressure propellant to obtain the desired pressure.
- the propellants customarily used are dichlorodifluoromethane (CCI F and monochlorodifluoroethane (CH CC1F each of which is more expensive than ethyl chloride.
- compositions of the invention therefore, supply increased pressure at reduced cost.
- a further advantage of the invention compositions is that in the event of a vapor phase leak in the aerosol container, the composition of the remaining liquefied gas propellant remains unchanged. When mixed propellants are used which are not of azeotropic composition the more volatile component is more readily lost Further advantage afforded by the invention is increased miscibility of common organic aerosol ingredients in the 36-37 mol percent ethyl chloride compositions over miscibility in dichlorotetrafiuoroethanes alone.
- the process of producing refrigeration which comprises evaporating, in the vicinity of a body to be cooled, a mixture consisting of dichlorotetrafluoroethane and ethyl chloride which mixture boils at a substantially constant temperature and functions as a substantially single substance, and in which mixture the mol percent of ethyl chloride is in the range of 22-50, and subsequently condensing the said mixture.
- the process of producing refrigeration which comprises evaporating, in the vicinity of a body to be cooled, a mixture consisting of dichlorotetrafluoroethane and approximately 36-37 mol percent of ethyl chloride which mixture boils at substantially constant temperature and functions as a substantially single substance, and subsequently condensing the said mixture.
Description
July 31, 1962 R. D. BROADLEY 3,047,506
REFRIGERATION PROCESS Filed Dec. 15, 1957 BOILING POINT (veo MM.H9v)-C. O!
CURVE B CURVEA o I l l I l l l l I lo 20 30 4o so e0 70 so 90 I00 MOL ETHYL CHLORIDE INVENTOR ROBERT D. BROADLEY ATTORNEY United States Patent Ofi ice 3,47,506 Patented July 31, 1962 This invention relates to azeotropic compositions containing dichlorotetrafluoroethane. These fluorine compounds are useful as refrigerants and as aerosol propellants.
Dichlorotetrafiuoroethanes are commercially produced as mixtures of the two isomers, one representative mixture containing mainly the symmetrical isomer CClFgCClF with a few percent of the unsymmetrical isomer OCl FCF and another typical mixture containing mainly the unsymmetrical isomer with a few percent of the symmetrical isomer. The boiling points of the pure isomers are 3.64 C. and 3.14" C. for the symmetrical and unsymmetrical isomers respectively; the boiling points of commercial products being intermediate these limits. Since the difference in boiling points of the two isomers is so small, minor composition variations are of no practical importance, and accordingly unless otherwise indicated the term "dichlorotetrafluoroethane as used herein is intended to embrace substantially pure CCI FCF or substantially pure CClF CClF or mixtures thereof in any proportions.
Objects of the invention include provision of dichlorotetrafluoroethane-ethyl chloride mixtures which boil at substantially constant temperature and function as a single substance. These mixtures are useful as refrigerants and as aerosol propellants. As refrigerants, such mixtures at lower cost afford increased pressure and greater refrigerating capacity with respect to refrigerating apparatus designed for use of dichlorotetrafluoroethane alone, and as aerosols such mixtures at lower cost provide increased pressure, and improved solubility for common aerosol ingredients.
Commercial dichlorotetrafluoroethanes boil in the range of 3.2 to 3.6 C. at normal atmospheric pressure, 760 mm. of Hg. In accordance with the invention it has been found that mixtures consisting of about 63-64 mol percent of commercial dichlorotetrafluoroethanes and 36-37 mol percent of ethyl chloride form azeotropes boiling in the range of about 1.1 and 1.4 C. Further, it has been found that the boiling point composition curve is very fiat and that mixtures containing ethyl chloride in the range of about 22-50 mol percent all boil between about 1.1 and 16 C., and that with regard to particular specific mixtures within the indicated 22-50 mol percent range, boiling points of such mixtures may vary only to the extent of about 0.2 C.
The boiling points of mixtures under consideration were determined with the following results:
In the foregoing tests, the specific material employed was a mixture of ethyl chloride and dichlorotetrafluoroethane which, as indicated by the 3.2" C. boiling point, was mostly CCl FCF plus a few percent of CClF CClF The data of Table I are shown graphically by curve A of the attached drawing.
Table II Mol percent ethyl chloride Boiling point (760 in solution: mm. Hg at 0 C), C.
In the tests of Table II, the specific material employed was a mixture of ethyl chloride and dichlorotetrafluoroethane which, as indicated by the 3.6 C. boiling point, was nearly pure CClF CClF containing very little CCl FCF The data of Table II are shown graphically by curve B of the drawing.
The above data and curves show that minimum-boiling azeot-ropes are formed each with approximately 36-37 mol percent of ethyl chloride. The ethyl chloride-commercial dichlorotetrafiuoroethane mixtures indicated afford the further advantage that there are only minor differences in boiling point when the composition is varied over a considerable range on either side of the 36-37 mol percent ethyl chloride compositions. Mixtures containing between about 22 to about 50 mol percent of ethyl chloride all boil between about 1.1 C. and about 1.6 C. It is noted that in both tests, each dealing with a mixture containing a specific dichlorotetrafiuoroethane, boiling points of the approximately 36-37 mol percent ethyl chloride compositions fall in the range of about 1.1-1.4" C., and temperature variation over the approximately 22-50 mol percent ethyl chloride range is only about 02 C. Hence, essentially no fractionation occurs on distillation over the approximate 22-50 ethyl chloride mol percent range. Moreover, in the case of other mixtures containing other specific dichlorotetrafluoroethanes, e.g. a mixture of ethyl chloride and a dichlorotetrafluoroethane consisting of say equal weight or mol percent parts of the isomers, the just mentioned boiling point range of 1.1- 1.4 C. and temperature variation range of only about 02 C. hold likewise.
For most advantageous refrigerant use, it is preferred to employ compositions at or close to the 36-37 mol percent ethyl chloride content in order to avoid even minor differences in liquid and vapor composition. However, in aerosol propellant use, differences in liquid and vapor composition are of lesser consequence, hence the whole range of 22-50 mol percent ethyl chloride composition may be employed to advantage. To insure non-flammability, compositions containing at least about 50 mol percent of dichlorotetrafluoroethane are preferred.
Apart from use of the indicated amounts of dichlorotetrafluoroethane and ethyl chloride, make-up of the compositions of the invention requires no special procedures. The dichlorotetrafluoroethane and the ethyl chloride em ployed should be substantially pure, and contain no substances deleteriously affecting use either as refrigerants or aerosol propellants. The compositions of the invention are chemically nonreactive, non-inflammable and substantially non-toxic.
It is known in the refrigerating art, with respect to equipment designed to utilize a particular refrigerant e.g. dichlorotetrafluoroethane, that it is often desirable to increase refrigerating capacities, and that, in general, capacity is proportional to the pressure of the gas at the suction side of the compressor. However, for a given item of equipment it is not possible to use a referigerant having a boiling point too far below that for which the equipment was designed because pressures would be too high and power input required would overload the compressor motor. A moderate increase in pressure is permissible, and use of a slightly lower boiling refrigerant affords increased capacity, other operating factors remaining constant. Substitution of the compositions of the invention for dichlorotetrafluoroethane in apparatus designed for use of dichlorotetrafluoroethane alone as the refrigerant eifects an increased refrigerating capacity of about Similarly, if a given refrigerating unit is equipped with motor designed to operate compressor at a given speed with normal 60 cycle current, use of such motor with 50 cycle current will lead to decreased motor speed and subsequent decrease in refrigerating capacity. The substitution of the compositions of the invention will substantially compensate for the decreased efficiency and restore a unit designed for dichiorotetrafluoroethane alone to near normal 60 cycle emciency. The compositions of the invention may be used as refrigerants in any cooling systems in which cooling is eifected by evaporation and expansion of liquid refrigerants such as domestic and commercial refrigerators, and domestic or commercial cooling or air-conditioning systems. As is well known in the refrigerating art, in these systems the expanded gas is compressed and condensed to a liquid and is recycled to the expansion stage.
For aerosol use the products of the invention supply distinct advantages. Whereas commercial dichlorotetrafiuoroethanes boil in the range of 3.23.6 C. and have vapor pressures in the range of 27.6-28.1 p.-s.i.g. at 70 R, such pressures are not sufficient to propel the aerosol product to :give the desired fine particle size in the spray. Consequently it is usually necessary to mix dichlorotetrafluoroethane with another higher pressure propellant to obtain the desired pressure. The propellants customarily used are dichlorodifluoromethane (CCI F and monochlorodifluoroethane (CH CC1F each of which is more expensive than ethyl chloride. The compositions of the invention, therefore, supply increased pressure at reduced cost. A further advantage of the invention compositions is that in the event of a vapor phase leak in the aerosol container, the composition of the remaining liquefied gas propellant remains unchanged. When mixed propellants are used which are not of azeotropic composition the more volatile component is more readily lost Further advantage afforded by the invention is increased miscibility of common organic aerosol ingredients in the 36-37 mol percent ethyl chloride compositions over miscibility in dichlorotetrafiuoroethanes alone. For example, Whereas only about 21% by weight of a dichlorotetrafluoroethane alone will dissolve in 75.6% strength ethanol, about 28% of such compositions will dissolve in 75.6% strength ethanol. Similarly, whereas only about 12% by weight of a dichlorotetrafiuoroethane alone will dissolve in 68.5% strength ethanol, about 17.5% by weight of such compositions will dissolve in the same strength alcohol. This feature permits lower strength alcohols to be used without sacrificing miscibility with the propellant; for example lower strength alcohols are desired to reduce astringency of cosmetic aerosol preparations. To express the advantage in a different way, assuming 20% of propellant in an aerosol formulation is required to produce the desired pressure, 75% strength alcohol is required to :'be miscible with a dichlorotetrafluoroethane alone, whereas only strength alcohol is required to be miscible with the compositions under consideration. This advantage increases within limits as the percent propellant required in the formulation is decreased. Other more striking differences in solubility of the 36-37 mol percent ethyl chloride compositions are as follows:
Table III Solubility Solubility percent percent in in 36-37 mol percent commercial OZH OI compositions diehlorotetrafluoroethane As compared with use of dichlorotetrafluoroethane alone, for either refrigerant or aerosol propellant purposes, the costwise advantages afforded by the invention are marked. Thus, by use of the compositions of the invention, not only are there obtained substantially improved pressure conditions, but in many instances as much as fifty mol percent of the relatively expensive chlorofluorocarbon maybe replaced by the relatively inexpensive ethyl chloride.
I claim:
1. The process of producing refrigeration which comprises evaporating, in the vicinity of a body to be cooled, a mixture consisting of dichlorotetrafluoroethane and ethyl chloride which mixture boils at a substantially constant temperature and functions as a substantially single substance, and in which mixture the mol percent of ethyl chloride is in the range of 22-50, and subsequently condensing the said mixture.
2. The process of producing refrigeration which comprises evaporating, in the vicinity of a body to be cooled, a mixture consisting of dichlorotetrafluoroethane and approximately 36-37 mol percent of ethyl chloride which mixture boils at substantially constant temperature and functions as a substantially single substance, and subsequently condensing the said mixture.
References Cited in the file of this patent UNITED STATES PATENTS
Claims (1)
1. THE PROCESS OF PRODUCING REFRIGERATION WHICH COMPRISES EVAPORATING, IN THE VICINITY OF A BODY TO BE COOLED, A MIXTURE CONSITING OF DICHLOROTETRAFLUOROETHANE AND ETHYL CHLORIDE WHICH MIXTURE BOILS AT A SUBSTANTIALLY CONSTANT TEMPERATURE AND FUNCTIONS AS A SUBSTANTIALLY SINGLE SUBSTANCE, AND IN WHICH MIXTURE THE MOL PERCENT OF ETHYL CHLORIDE IS IN THE RANGE OF 22-50, AND SUBSEQUENTLY CONDENSING THE SAID MIXTURE.
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US702646A US3047506A (en) | 1957-12-13 | 1957-12-13 | Refrigeration process |
Applications Claiming Priority (1)
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US702646A US3047506A (en) | 1957-12-13 | 1957-12-13 | Refrigeration process |
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US3047506A true US3047506A (en) | 1962-07-31 |
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US702646A Expired - Lifetime US3047506A (en) | 1957-12-13 | 1957-12-13 | Refrigeration process |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3387425A (en) * | 1964-12-08 | 1968-06-11 | Allied Chem | Process for preparing aerosol packages |
US3394878A (en) * | 1965-08-25 | 1968-07-30 | Du Pont | Azeotropic compositions |
US3505232A (en) * | 1967-01-09 | 1970-04-07 | Allied Chem | Azeotropic mixture |
US4510064A (en) * | 1984-02-13 | 1985-04-09 | Robert D. Stevens | Mixture of three refrigerants |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2101993A (en) * | 1932-04-30 | 1937-12-14 | Gen Motors Corp | Refrigerant mixture and the method of using the same |
US2255584A (en) * | 1937-12-11 | 1941-09-09 | Borg Warner | Method of and apparatus for heat transfer |
US2449114A (en) * | 1944-10-25 | 1948-09-14 | Gebauer Chemical Company | Lubricating composition |
US2524590A (en) * | 1946-04-22 | 1950-10-03 | Carsten F Boe | Emulsion containing a liquefied propellant gas under pressure and method of spraying same |
US2630686A (en) * | 1951-03-13 | 1953-03-10 | Carrier Corp | Refrigeration system containing novel refrigerant |
-
1957
- 1957-12-13 US US702646A patent/US3047506A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2101993A (en) * | 1932-04-30 | 1937-12-14 | Gen Motors Corp | Refrigerant mixture and the method of using the same |
US2255584A (en) * | 1937-12-11 | 1941-09-09 | Borg Warner | Method of and apparatus for heat transfer |
US2449114A (en) * | 1944-10-25 | 1948-09-14 | Gebauer Chemical Company | Lubricating composition |
US2524590A (en) * | 1946-04-22 | 1950-10-03 | Carsten F Boe | Emulsion containing a liquefied propellant gas under pressure and method of spraying same |
US2630686A (en) * | 1951-03-13 | 1953-03-10 | Carrier Corp | Refrigeration system containing novel refrigerant |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3387425A (en) * | 1964-12-08 | 1968-06-11 | Allied Chem | Process for preparing aerosol packages |
US3394878A (en) * | 1965-08-25 | 1968-07-30 | Du Pont | Azeotropic compositions |
US3505232A (en) * | 1967-01-09 | 1970-04-07 | Allied Chem | Azeotropic mixture |
US4510064A (en) * | 1984-02-13 | 1985-04-09 | Robert D. Stevens | Mixture of three refrigerants |
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