Compositions including a three carbon cyclic fluoroether

Abstract

Refrigerant compositions include mixtures of perfluorooxetane and perfluoromethyl ethyl ether or dimethyl ether; 2,2,4,4,5,5-hexafluoro-1,3-dioxolane and cyclopropane or dimethyl ether; 2,2,3,4,4-pentafluorooxetane and difluoromethyl(trifluoromethyl)sulfide or 1-trifluoromethoxy-2,2,2-trifluoroethane; 2,2,4,4-tetrafluorooxetane and 1-difluoromethoxy-1,1,2,2-tetrafluoroethane or 1-difluoromethoxy-1,2,2,2-tetrafluoroethane; 2,2,3,3-tetrafluorooxetane and 1-difluoromethoxy-1,1,2,2-tetrafluoroethane or 1-difluoromethoxy-1,2,2,2-tetrafluoroethane.

Description

FIELD OF THE INVENTION

This invention relates to refrigerant compositions that include at least one three carbon cyclic fluoroether. These compositions are useful as cleaning agents, expansion agents for polyolefins and polyurethanes, aerosol propellants, refrigerants, heat transfer media, gaseous dielectrics, fire extinguishing agents, power cycle working fluids, polymerization media, particulate removal fluids, carrier fluids, buffing abrasive agents, and displacement drying agents.

BACKGROUND OF THE INVENTION

Fluorinated hydrocarbons have many uses, one of which is as a refrigerant. Such refrigerants include trichlorofluoromethane (CFC-11) dichlorodifluoromethane (CFC-12) and chlorodifluoromethane (HCFC-22).

In recent years it has been pointed out that certain kinds of fluorinated hydrocarbon refrigerants released into the atmosphere may adversely affect the stratospheric ozone layer. Although this proposition has not yet been completely established, there is a movement toward the control of the use and the production of certain chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs) under an international agreement.

Accordingly, there is a demand for the development of refrigerants that have a lower ozone depletion potential than existing refrigerants while still achieving an acceptable performance in refrigeration applications.

In refrigeration applications, a refrigerant is often lost during operation through leaks in shaft seals, hose connections, soldered joints and broken lines. In addition, the refrigerant may be released to the atmosphere during maintenance procedures on refrigeration equipment. If the refrigerant is not a pure component or an azeotropic or azeotrope-like composition, the refrigerant composition may change when leaked or discharged to the atmosphere from the refrigeration equipment, which may cause the refrigerant to become flammable or to have poor refrigeration performance.

Accordingly, it is desirable, if possible, to use as a refrigerant a single compound or an azeotropic or azeotrope-like composition of more than one compound.

It is also desirable to find replacements for CFCs and HCFCs for use as a cleaning agent or solvent to clean, for example, electronic circuit boards. It is preferred that the cleaning agents be azeotropic or azeotrope-like because in vapor degreasing operations the cleaning agent is generally redistilled and reused for final rinse cleaning.

Replacements for CFCs and HCFCs may also useful as blowing agents in the manufacture of closed-cell polyurethane, phenolic and thermoplastic foams, as propellants in aerosols, as heat transfer media, gaseous dielectrics, fire extinguishing agents, power cycle working fluids such as for heat pumps, inert media for polymerization reactions, fluids for removing particulates from metal surfaces, as carrier fluids that may be used, for example, to place a fine film of lubricant on metal parts, as buffing abrasive agents to remove buffing abrasive compounds from polished surfaces such as metal, as displacement drying agents for removing water, such as from jewelry or metal parts, as resist developers in conventional circuit manufacturing techniques including chlorine-type developing agents, or as strippers for photoresists when used with, for example, a chlorohydrocarbon such as 1,1,1-trichloroethane or trichloroethylene.

SUMMARY OF THE INVENTION

The present invention relates to the discovery of compositions of perfluorooxetane (C-216E) and perfluoromethyl ethyl ether (218E) or dimethyl ether (DME); 2,2,4,4,5,5-hexafluoro-1,3-dioxolane (C-216E2) and cyclopropane or dimethyl ether (DME); 2,2,3,4,4-pentafluorooxetane (C-225eE.alpha..beta.) and difluoromethyl(trifluoromethyl)sulfide (125S) or 1-trifluoromethoxy-2,2,2-trifluoroethane (236faE); 2,2,4,4-tetrafluorooxetane (C-234fE.alpha..beta.) and 1-difluoromethoxy-1,1,2,2-tetrafluoroethane (236caE) or 1-difluoromethoxy-1,2,2,2-tetrafluoroethane (236eaE.beta..gamma.); 2,2,3,3-tetrafluorooxetane (C-234fE.beta..gamma.) and 1-difluoromethoxy-1,1,2,2-tetrafluoroethane (236caE) or 1-difluoromethoxy-1,2,2,2-tetrafluoroethane (236eaE.beta..gamma.). This invention also relates to the discovery of azeotropic or azeotrope-like compositions comprising effective amounts of these compositions to form azeotropic or azeotrope-like compositions.

These compositions, which have little or no ozone depletion potential and which present environmentally acceptable alternatives to CFCs and HCFCs, are useful as refrigerants, cleaning agents, expansion agents for polyolefins and polyurethanes, aerosol propellants, heat transfer media, gaseous dielectrics, fire extinguishing agents, power cycle working fluids, polymerization media, particulate removal fluids, carrier fluids, buffing abrasive agents, and displacement drying agents.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graph of the vapor/liquid equilibrium curve for mixtures of C-216E/218E at 25.degree. C.;

FIG. 2 is a graph of the vapor/liquid equilibrium curve for mixtures of C-216E/DME at 25.degree. C.;

FIG. 3 is a graph of the vapor/liquid equilibrium curve for mixtures of C-216E2/cyclopropane at 25.degree. C.;

FIG. 4 is a graph of the vapor/liquid equilibrium curve for mixtures of C-216E2/DME at 25.degree. C.;

FIG. 5 is a graph of the vapor/liquid equilibrium curve for mixtures of C-225eE.alpha..beta./125S at 25.degree. C.;

FIG. 6 is a graph of the vapor/liquid equilibrium curve for mixtures of C-225eE.alpha..beta./236faE at 25.degree. C.;

FIG. 7 is a graph of the vapor/liquid equilibrium curve for mixtures of C-234fE.alpha..beta./236cae at 25.degree. C.;

FIG. 8 is a graph of the vapor/liquid equilibrium curve for mixtures of C-234fE.alpha..beta./236eaE.beta..gamma. at 25.degree. C.;

FIG. 9 is a graph of the vapor/liquid equilibrium curve for mixtures of C-234fE.beta..gamma./236caE at 25.degree. C.; and

FIG. 10 is a graph of the vapor/liquid equilibrium curve for mixtures of C-234fE.beta..gamma./236eaE.beta..gamma. at 25.degree. C.

DETAILED DESCRIPTION

The present invention relates to the discovery of compositions of C-216E and 218E or DME; C-216E2 and cyclopropane or DME; C-225eE.alpha..beta. and 125S or 236faE; C-234fE.alpha..beta. and 236caE or 236eaE.beta..gamma.; C-234fE.beta..gamma. and 236caE or 236eaE.beta..gamma.. This invention also relates to the discovery of azeotropic or azeotrope-like compositions comprising effective amounts of these compositions to form azeotropic or azeotrope-like compositions. 1-99 wt. % of each of the above components can be used as refrigerants.

The components of the refrigerants in this invention include the following:

1. Perfluorooxetane (C-216E or ##STR1## boiling point=-29.2.degree. C.), 2. 2,2,4,4,5,5-hexafluoro-1,3-dioxolane (C-216E2 or C.sub.3 F.sub.6 O.sub.2, having a structure of ##STR2## boiling point=-22.1.degree. C.), 3. 2,2,3,4,4-pentafluorooxetane (C-225eE.alpha..beta., or C.sub.3 HF.sub.5 O, having a structure of ##STR3## boiling point=3.4.degree. C.), 4. 2,2,4,4-tetrafluorooxetane (C-234fE.alpha..beta., or C.sub.3 H.sub.2 F.sub.4, having a structure of ##STR4## boiling point=21.2.degree. C.), 5. 2,2,3,3-tetrafluorooxetane (C-234fE.beta..gamma., or C.sub.3 H.sub.2 F.sub.4 O, having a structure of ##STR5## boiling point=28.degree. C.), 6. Perfluoromethyl ethyl ether (218E, or CF.sub.3 OCF.sub.2 CF.sub.3, boiling point=-23.3.degree. C.), 7. Dimethyl ether (DME, or CH.sub.3 OCH.sub.3), 8. Cyclopropane, 9. difluoromethyl(trifluoromethyl)sulfide (125S or CHF.sub.2 SCF.sub.3, boiling point=1.0.degree. C.) 10. 1-trifluoromethoxy-2,2,2-trifluoroethane (236faE, or CF.sub.3 OCH.sub.2 CF.sub.3, boiling point=5.6.degree. C.), 11. 1-difluoromethoxy-1,1,2,2-tetrafluoroethane (236caE, or CHF.sub.2 OCF.sub.2 CHF.sub.2, boiling point=28.5.degree. C.), and 12. 1-difluoromethoxy-1,2,2,2-tetrafluoroethane (236eaE.beta..gamma., or CHF.sub.2 OCHFCF.sub.3, boiling point=23.2.degree. C.).

C-216E (CAS Reg. No. 425-82-1) can be made by electrochemical fluorination of trimethylene oxide (oxetane) in anhydrous hydrogen fluoride as disclosed by Kauck and Simons in U.S. Pat. No. 2,594,272.

C-216E2 (CAS Reg. No. 21297-65-4) has been prepared by UV irradiation of perfluoro-b-oxa-d-valerolactone in the vapor or liquid phase as reported by Throckmorton in J. Org.Chem., Vol. 34, pp. 3438-3440 (1969). The lactone was prepared by the reaction of KF with perfluorooxydiacetyl chloride.

C-225eE.alpha..beta. (CAS Reg. No. 144109-03-5) may be prepared by direct fluorination of trimethylene oxide (cyclo-CH.sub.2 CH.sub.2 CH.sub.2 O--) using techniques described by Lagow and Margrave in Progress in Inorganic Chemistry., Vol. 26, pp. 161-210 (1979) or by Adcock and Cherry in Ind. Eng. Chem. Res., Vol. 26, pp. 208-215 (1987). The direct fluorination is carried out to the desired level of fluorine incorporation into the starting material, and products recovered by fractional distillation.

C-234fE.alpha..beta. may be prepared by direct fluorination of trimethylene oxide(cyclo-CH.sub.2 CH.sub.2 CH.sub.2 O--) using techniques described by Lagow and Margrave in Progress in Inorganic Chemistry, Vol. 26, pp. 161-210 (1979) or by Adcock and Cherry in Ind. Eng. Chem. Res., Vol. 26, pp. 208-215 (1987). The direct fluorination is carried out to the desired level of fluorine incorporation into the starting material, and products recovered by fractional distillation.

C-234fE.beta..gamma. (CAS Reg. No. 765-63-9) has been prepared by Weinmayr (J. Or Chem., Vol. 28, pp. 492-494 (1963)) as a by-product from the reaction of TFE with formaldehyde in HF.

218E (CAS Reg. No. 665-16-7) has been made by direct fluorination of CF.sub.3 OCH.sub.2 CF.sub.3 (prepared by reaction of CF.sub.3 OF with vinylidene fluoride) as reported by Sekiya and Ueda in Chemistry Letters, pp. 609-612 (1990).

125S (CAS Reg. No. 371-72-2) has been prepared by the photolysis of CF.sub.2 HC(O)OSCF.sub.3 as described by Yu et. al. in Inorg. Chem., Vol. 13, pages 484-486 (1974).

236faE (CAS Reg. No. 20193-67-3) has been prepared by reaction of 2,2,2-trifluoroethanol with carbonyl fluoride to give the intermediate, CF.sub.3 CH.sub.2 OCOF, which was in turn reacted with sulfur tetrafluoride at 150.degree.-200.degree. C. to give the product as disclosed by Eisemann in U.S. Pat. No. 3,394,878.

236caE (CAS Reg. No. 32778-11-3) has been prepared by fluorination of CHCl.sub.2 OCF.sub.2 CHF.sub.2 (prepared in turn by chlorination of CH.sub.3 OCF.sub.2 CHF.sub.2) using anhydrous hydrogen fluoride with antimony pentachloride catalyst as reported by Terrell, et. al. in J. Medicinal Chem., Vol. 15, pp. 604-606 (1972).

236eaE.beta..gamma. (CAS Reg. No. 5704 1-67-5) has been prepared by chlorination of methoxy acetyl chloride to give the intermediate, CHCl.sub.2 OCHC.sub.1 COCl, which was isolated and reacted with sulfur tetrafluoride at 150.degree. C. to give the product as disclosed by Halpern and Robin in U.S. Pat. No. 4,888,139.

The present invention also relates to the discovery of azeotropic or azeotrope-like compositions of effective amounts of C-216E and 218E or DME; C-216E2 and cyclopropane or DME; C-225eE.alpha..beta. and 125S or 236faE; C-234fE.alpha..beta. and 236caE or 236eaE.beta..gamma.; C-234fE.beta..gamma. and 236caE or 236eaE.beta..gamma. to form an azeotropic or azeotrope-like composition.

By "azeotropic" composition is meant a constant boiling liquid admixture of two or more substances that behaves as a single substance. One way to characterize an azeotropic composition is that the vapor produced by partial evaporation or distillation of the liquid has the same composition as the liquid from which it was evaporated or distilled., that is, the admixture distills/refluxes without compositional change. Constant boiling compositions are characterized as azeotropic because they exhibit either a maximum or minimum boiling point, as compared with that of the non-azeotropic mixtures of the same components.

By "azeotrope-like" composition is meant a constant boiling, or substantially constant boiling, liquid admixture of two or more substances that behaves as a single substance. One way to characterize an azeotrope-like composition is that the vapor produced by partial evaporation or distillation of the liquid has substantially the same composition as the liquid from which it was evaporated or distilled, that is, the admixture distills/refluxes without substantial composition change. Another way to characterize an azeotrope-like composition is that the bubble point vapor pressure and the dew point vapor pressure of the composition at a particular temperature are substantially the same.

It is recognized in the art that a composition is azeotrope-like if, after 50 weight percent of the composition is removed such as by evaporation or boiling off, the difference in vapor pressure between the original composition and the composition remaining after 50 weight percent of the original composition has been removed is less than 10 percent, when measured in absolute units. By absolute units, it is meant measurements of pressure and, for example, psia, atmospheres, bars, torr, dynes per square centimeter, millimeters of mercury, inches of water and other equivalent terms well known in the art. If an azeotrope is present, there is no difference in vapor pressure between the original composition and the composition remaining after 50 weight percent of the original composition has been removed.

Therefore, included in this invention are compositions of effective amounts of C-216E and 218E or DME; C-216E2 and cyclopropane or DME; C-225eE.alpha..beta. and 125S or 236faE; C-234fE.alpha..beta. and 236caE or 236eaE.beta..gamma.; C-234fE.alpha..beta. an 236caE or 236eaE.beta..gamma., such that after 50 weight percent of an original composition is evaporated or boiled off to produce a remaining composition, the difference in the vapor pressure between the original composition and the remaining composition is 10 percent or less.

For compositions that are azeotropic, there is usually some range of compositions around the azeotrope point that, for a maximum boiling azeotrope, have boiling points at a particular pressure higher than the pure components of the composition at that pressure and have vapor pressures at a particular temperature lower than the pure components of the composition at that temperature, and that, for a minimum boiling azeotrope, have boiling points at a particular pressure lower than the pure components of the composition at that pressure and have vapor pressures at a particular temperature higher than the pure components of the composition at that temperature. Boiling temperatures and vapor pressures above or below that of the pure components are caused by unexpected intermolecular forces between and among the molecules of the compositions, which can be a combination of repulsive and attractive forces such as van der Waals forces and hydrogen bonding.

The range of compositions that have a maximum or minimum boiling point at a particular pressure, or a maximum or minimum vapor pressure at a particular temperature, may or may not be coextensive with the range of compositions that have a change in vapor pressure of less than about 10% when 50 weight percent of the composition is evaporated. In those cases where the range of compositions that have maximum or minimum boiling temperatures at a particular pressure, or maximum or minimum vapor pressures at a particular temperature, are broader than the range of compositions that have a change in vapor pressure of less than about 10% when 50 weight percent of the composition is evaporated, the unexpected intermolecular forces are nonetheless believed important in that the refrigerant compositions having those forces that are not substantially constant boiling may exhibit unexpected increases in the capacity or efficiency versus the components of the refrigerant composition.

The components of the compositions of this invention have the following vapor pressures at 25.degree. C.

______________________________________Components Psia kPa______________________________________C-216E 100.3 692C-216E2 76.7 529C-225eE.alpha..beta. 31.1 214C-234fE.alpha..beta. 16.7 115C-234fE.beta..gamma. 13.3 91218E 83.8 578DME 85.7 591125S 34.5 238236faE 29.6 204236caE 12.9 89236eaE.beta..gamma. 15.7 108cyclopropane 105.0 724______________________________________

Substantially constant boiling, azeotropic or azeotrope-like compositions of this invention comprise the following (all compositions are measured at 25.degree. C.):

______________________________________ WEIGHT RANGES PREFERREDCOMPONENTS (wt. %/wt/%) (wt. %/wt. %)______________________________________C-216E/218E 1-99/1-99 20-99/1-80C-216E/DME 1-99/1-99 20-99/1-80C-216E2/cyclopropane 0.9-99/1-99.1 0.9-99/1-99.1C-216E2/DME 1-99/1-99 20-99/1-80C-225eE.alpha..beta./125S 1-99/1-99 1-80/20-99C-225eE.alpha..beta./236faE 1-99/1-99 1-99/1-99C-234fE.alpha..beta./236caE 1-99/1-99 15-99/1-85C-234fE.alpha..beta./236eaE.beta..gamma. 1-99/1-99 1-99/1-99C-234fE.beta..gamma./236caE 1-99/1-99 1-99/1-99C-234fE.beta..gamma./236eaE.beta..gamma. 1-99/1-99 1-80/20-99______________________________________

For purposes of this invention, "effective amount" is defined as the amount of each component of the inventive compositions which, when combined, results in the formation of an azeotropic or azeotrope-like composition. This definition includes the amounts of each component, which amounts may vary depending on the pressure applied to the composition so long as the azeotropic or azeotrope-like compositions continue to exist at the different pressures, but with possible different boiling points.

Therefore, effective amount includes the amounts, such as may be expressed in weight percentages, of each component of the compositions of the instant invention which form azeotropic or azeotrope-like compositions at temperatures or pressures other than as described herein.

For the purposes of this discussion, azeotropic or constant-boiling is intended to mean also essentially azeotropic or essentially-constant boiling. In other words, included within the meaning of these terms are not only the true azeotropes described above, but also other compositions containing the same components in different proportions, which are true azeotropes at other temperatures and pressures, as well as those equivalent compositions which are part of the same azeotropic system and are azeotrope-like in their properties. As is well recognized in this art, there is a range of compositions which contain the same components as the azeotrope, which will not only exhibit essentially equivalent properties for refrigeration and other applications, but which will also exhibit essentially equivalent properties to the true azeotropic composition in terms of constant boiling characteristics or tendency not to segregate or fractionate on boiling.

It is possible to characterize, in effect, a constant boiling admixture which may appear under many guises, depending upon the conditions chosen, by any of several criteria:

The composition can be defined as an azeotrope of A, B, C (and D . . . ) since the very term "azeotrope" is at once both definitive and limitative, and requires that effective amounts of A, B, C (and D . . . ) for this unique composition of matter which is a constant boiling composition. It is well known by those skilled in the art, that, at different pressures, the composition of a given azeotrope will vary at least to some degree, and changes in pressure will also change, at least to some degree, the boiling point temperature. Thus, an azeotrope of A, B, C (and D . . . ) represents a unique type of relationship but with a variable composition which depends on temperature and/or pressure. Therefore, compositional ranges, rather than fixed compositions, are often used to define azeotropes. The composition can be defined as a particular weight percent relationship or mole percent relationship of A, B, C (and D . . . ), while recognizing that such specific values point out only one particular relationship and that in actuality, a series of such relationships, represented by A, B, C (and D . . . ) actually exist for a given azeotrope, varied by the influence of pressure. An azeotrope of A, B, C (and D . . . ) can be characterized by defining the compositions as an azeotrope characterized by a boiling point at a given pressure, thus giving identifying characteristics without unduly limiting the scope of the invention by a specific numerical composition, which is limited by and is only as accurate as the analytical equipment available.

The azeotrope or azeotrope-like compositions of the present invention can be prepared by any convenient method including mixing or combining the desired amounts. A preferred method is to weigh the desired component amounts and thereafter combine them in an appropriate container.

Specific examples illustrating the invention are given below. Unless otherwise stated therein, all percentages are by weight. It is to be understood that these examples are merely illustrative and in no way are to be interpreted as limiting the scope of the invention.

EXAMPLE 1

Phase Study

A phase study shows the following compositions are azeotropic, all at 25.degree. C.

______________________________________ Weight percent of Vapor Press.Composition No. the components psia (kPa)______________________________________C-216E/218E 81.9/18.1 101.2 698C-216E/DME 82.1/17.9 111.2 767C-216E2/cyclopropane 0.9/99.1 105. 724C-216E2/DME 69.2/30.8 97.5 672C-225eE.alpha..beta./125S 7.2/92.8 34.5 238C-225eE.alpha..beta./236faE 64.9/35.1 31.7 219C-234fE.alpha..beta./236caE 90.7/9.3 16.8 116C-234fE.alpha..beta./236eaE.beta..gamma. 57.5/42.5 17.8 123C-234fE.beta..gamma./236caE 51.8/48.2 14.4 99C-234fE.beta..gamma./236eaE.beta..gamma. 28.6/71.4 16.3 112______________________________________

EXAMPLE 2

Impact of Vapor Leakage on Vapor Pressure at 25.degree. C.

A vessel is charged with an initial composition at 25.degree. C., and the vapor pressure of the composition is measured. The composition is allowed to leak from the vessel, while the temperature is held constant at 25.degree. C., until 50 weight percent of the initial composition is removed, at which time the vapor pressure of the composition remaining in the vessel is measured. The results are summarized below.

______________________________________ INITIAL 50% LEAK DELTAWT % A/WT % B PSIA KPA PSIA KPA % P______________________________________C-216E/218E81.9/18.1 101.2 698 101.2 698 0.090./10 101. 696 101. 696 0.099/1 100.4 692 100.4 692 0.060/40 100.1 690 99.9 689 0.240/60 97.1 669 96.3 664 0.820/80 91.9 634 90.7 625 1.310/90 88.3 609 87.3 602 1.11/99 84.3 581 84.2 581 0.1C-216E/DME82.1/17.9 111.2 767 111.2 767 0.099/1 102.1 704 101.6 701 0.560/40 107.6 742 105.3 726 2.140/60 101.9 703 96.4 665 5.430/70 98.4 678 92.4 637 6.120/80 94.6 652 89.3 616 5.61/99 86.2 594 85.8 592 0.5C-216E2/cyclopropane0.9/99.1 105. 724 105. 724 0.030/70 104.7 722 104.7 722 0.070/30 100.7 694 99.7 687 1.85/15 94.9 654 92.6 638 2.499/1 78.8 543 78.1 538 0.9C-216E2/DME69.2/30.8 97.5 672 97.5 672 0.085/15 95.1 656 93.8 647 1.499/1 79.4 547 78.2 539 1.540/60 94.6 652 93.0 641 1.720/80 90.7 625 88.7 612 3.31/99 86.0 593 85.8 592 0.2C-225eE.alpha..beta./125S7.2/92.8 34.5 238 34.5 238 0.01/99 34.5 238 34.5 238 0.030/70 34.3 236 34.3 236 0.060/40 33.5 231 33.4 230 0.380/20 32.5 224 32.4 223 0.399/1 31.2 215 31.2 215 0.0C-225eE.alpha..beta./236faE64.9/35.1 31.7 219 31.7 219 0.080/20 31.6 218 31.6 218 0.099/1 31.1 214 31.1 214 0.030/70 31.1 214 31.1 214 0.01/99 29.7 205 29.7 205 0.0C-234fE.alpha..beta./236caE90.7/9.3 16.8 116 16.8 116 0.099/1 16.8 116 16.8 116 0.060/40 16.4 113 16.3 112 0.630/70 15.2 105 14.9 103 2.15/85 14.3 99 14. 97 2.11/99 13. 90 13. 90 0.0C-234fE.alpha..beta./236eaE.beta..gamma. 17.8 123 17.8 123 0.057.5/42.580/20 17.5 121 17.5 121 0.099/1 16.8 116 16.8 116 0.020/80 17. 117 16.9 117 0.61/99 15.8 109 15.8 109 0.0C-234fE.beta..gamma./236caE51.8/48.2 14.4 99 14.4 99 0.025/75 14. 97 14. 97 0.01/99 13. 90 13. 90 0.075/25 14.1 97 14.1 97 0.099/1 13.3 92 13.3 92 0.0C-234fE.beta..gamma./236eaE.beta..gamma.28.6/71.4 16.3 112 16.3 112 0.015/85 16.2 112 16.2 112 0.01/99 15.7 108 15.7 108 0.060/40 15.8 109 15.6 108 1.380/20 14.9 103 14.5 100 2.799/1 13.4 92 13.3 92 0.7______________________________________

The results of this Example show that these compositions are azeotropic or azeotrope-like because when 50 wt. % of an original composition is removed, the vapor pressure of the remaining composition is within about 10% of the vapor pressure of the original composition, at a temperature of 25.degree. C.

EXAMPLE 3

Impact of Vapor Leakage at 50.degree. C.

A leak test is performed on composition of C-216E and DME, at the temperature of 50.degree. C. The results are summarized below.

______________________________________ INITIAL 50% LEAK DELTAWT % A/WT % B PSIA KPA PSIA KPA % P______________________________________C216E/DME82.7/17.3 212.0 1462 212.0 1462 0.099/1 197.0 1358 196.2 1353 0.460/40 205.0 1413 201.0 1386 2.040/60 194.3 1340 185.1 1276 4.720/80 181.1 1249 172.5 1189 4.71/99 166.4 1147 165.8 1143 0.4______________________________________

EXAMPLE 4

Refrigerant Performance

The following table shows the performance of various refrigerants. The data are based on the following conditions.

Evaporator temperature 48.0.degree. F. (8.9.degree. C.) Condenser temperature 115.0.degree. F. (46.1.degree. C.) Subcooled 12.0.degree. F. (6.7.degree. C.) Return gas temperature 65.0.degree. F. (18.3.degree. C.) Compressor efficiency is 75%.

The refrigeration capacity is based on a compressor with a fixed displacement of 3.5 cubic feet per minute and 75% volumetric efficiency. Capacity is intended to mean the change in enthalpy of the refrigerant in the evaporator per pound of refrigerant circulated, i.e. the heat removed by the refrigerant in the evaporator per time. Coefficient of performance (COP) is intended to mean the ratio of the capacity to compressor work. It is a measure of refrigerant energy efficiency.

__________________________________________________________________________ Evap. Cond. CapacityRefrig. Press. Press. Comp. Dis. BTU/minComp. Psia (kPa) Psia (kPa) Temp. .degree.F. (.degree.C.) COP (kw)__________________________________________________________________________C-216E/218E5.0/95.0 51 (352) 154 (1062) 122 (50) 4.06 189 (3.3)81.9/18.1 57 (393) 161 (1110) 123 (50.6) 4.15 205 (3.6)95.0/5.0 58 (400) 163 (1124) 123 (50.6) 4.17 208 (3.7)C-216E/DME5.0/95.0 54 (372) 155 (1069) 165 (73.9) 5.00 254 (4.5)82.1/17.9 83 (572) 221 (1524) 135 (57.2) 4.26 291 (5.1)95.0/5.0 69 (476) 190 (1310) 128 (53.3) 4.25 248 (4.4)C-216E2/cyclopropane0.9/99.1 66 (455) 178 (1227) 174 (78.9) 4.87 289 (5.1)95.0/5.0 53 (365) 154 (1062) 125 (51.7) 4.43 213 (3.8)C-216E2/DME5.0/95.0 52 (359) 150 (1034) 166 (74.4) 4.88 242 (4.3)69.2/30.8 61 (421) 172 (1186) 140 (60.0) 4.63 254 (4.5)95.0/5.0 52 (359) 153 (1055) 124 (51.1) 4.41 209 (3.7)C-225eE.alpha..beta./125S1.0/99.0 20 (138) 66 (455) 139 (59.4) 4.85 102 (1.8)7.2/92.8 19 (131) 66 (455) 138 (58.9) 4.85 101 (1.8)95.0/5.0 18 (124) 59 (407) 130 (54.4) 4.82 91 (1.6)C-225eE.alpha..beta./236faE5.0/95.0 17 (117) 59 (407) 127 (52.8) 4.71 86 (1.5)64.9/35.1 17 (117) 59 (407) 129 (53.9) 4.78 89 (1.6)95.0/5.0 18 (124) 59 (407) 130 (54.4) 4.82 90 (1.6)C-234fE.alpha..beta./236caE5.0/95.0 7 (48) 28 (193) 134 (56.7) 4.91 42 (0.7)90.7/9.3 9 (62) 32 (221) 135 (57.2) 4.96 51 (0.9)99.0/1.0 9 (62) 33 (228) 135 (57.2) 4.97 51 (0.9)C-234fE.alpha..beta./236eaE.beta..gamma.5.0/95.0 8 (55) 33 (228) 133 (56.1) 4.88 50 (0.9)57.5/42.5 9 (62) 33 (228) 134 (56.7) 4.93 50 (0.9)95.0/5.0 9 (62) 33 (228) 135 (57.2) 4.96 52 (0.9)C-234fE.beta..gamma./236caE5.0/95.0 7 (48) 27 (186) 134 (56.7) 4.91 41 (0.7)51.8/48.2 7 (48) 28 (193) 135 (57.2) 4.96 43 (0.8)95.0/5.0 7 (48) 26 (179) 137 (58.3) 4.99 42 (0.7)C-234fE.beta..gamma./236eaE.beta..gamma.5.0/95.0 8 (55) 33 (228) 133 (56.1) 4.88 49 (0.9)28.6/71.4 8 (55) 31 (214) 134 (56.7) 4.92 48 (0.8)95.0/5.0 7 (48) 26 (179) 137 (58.3) 4.99 42 (0.7)__________________________________________________________________________

EXAMPLE 5

This Example is directed to measurements of the liquid/vapor equilibrium curves for the mixtures in FIGS. 1-10.

Turning to FIG. 1, the upper curve represents the composition of the liquid, and the lower curve represents the composition of the vapor.

The data for the compositions of the liquid in FIG. 1 are obtained as follows. A stainless steel cylinder is evacuated, and a weighed amount of C-216E is added to the cylinder. The cylinder is cooled to reduce the vapor pressure of C-216E, and then a weighed amount of 218E is added to the cylinder. The cylinder is agitated to mix the C-216E and 218E, and then the cylinder is placed in a constant temperature bath until the temperature comes to equilibrium at 25.degree. C., at which time the vapor pressure of the C-216E and 218E in the cylinder is measured. Additional samples of liquid are measured the same way, and the results are plotted in FIG. 1.

The curve which shows the composition of the vapor is calculated using an ideal gas equation of state.

Vapor/liquid equilibrium data are obtained in the same way for the mixtures shown in FIGS. 2-10.

The data in FIGS. 1-10 show that at 25.degree. C., there are ranges of compositions that have vapor pressures higher than the vapor pressures of the pure components of the composition at that same temperature. As stated earlier, the higher than expected pressures of these compositions may result in an unexpected increase in the refrigeration capacity and efficiency for these compositions versus the pure components of the compositions.

The compositions of this invention, including the azeotropic or azeotrope-like compositions, may be used to produce refrigeration by condensing the compositions and thereafter evaporating the condensate in the vicinity of a body to be cooled. These compositions may also be used to produce heat by condensing the refrigerant in the vicinity of the body to be heated and thereafter evaporating the refrigerant.

The novel compositions of the invention are particularly suitable for replacing refrigerants that may affect the ozone layer, including R-11, R-12, R-22, R-114 and R-502.

In addition to refrigeration applications, the compositions of this invention, including the azeotropic or azeotrope-like compositions, are also useful as aerosol propellants, heat transfer media, gaseous dielectrics, fire extinguishing agents, expansion agents for polyolefins and polyurethanes and power cycle working fluids.

ADDITIONAL COMPOUNDS

Other components, such as aliphatic hydrocarbons having a boiling point of -60.degree. to +60.degree. C., hydrofluorocarbonalkanes having a boiling point of -60.degree. to +60.degree. C., hydrofluoropropanes having a boiling point of between -60.degree. to +60.degree. C., hydrocarbon esters having a boiling point between -60.degree. to +60.degree. C., hydrochlorofluorocarbons having a boiling point between -60.degree. to +60.degree. C., hydrofluorocarbons having a boiling point of -60.degree. to +60.degree. C., hydrochlorocarbons having a boiling point between -60.degree. to +60.degree. C., chlorocarbons and perfluorinated compounds, can be added to the azeotropic or azeotrope-like compositions described above without substantially changing the properties thereof, including the constant boiling behavior, of the compositions.

Additives such as lubricants, corrosion inhibitors, surfactants, stabilizers, dyes and other appropriate materials may be added to the novel compositions of the invention for a variety of purposes provides they do not have an adverse influence on the composition for its intended application. Preferred lubricants include esters having a molecular weight greater than 250.

Claims

1. An azeotropic or azeotrope-like composition consisting essentially of about 80 to about 99 weight percent 2,2,4,4-tetrafluorooxetane and about 1 to about 20 weight percent 1-difluoromethoxy-1,1,2,2-tetrafluoroethane wherein said composition has a vapor pressure of about 16.8 psia at 25.degree. C., or about 15 to about 99 weight percent 2,2,4,4-tetrafluorooxetane and about 1 to about 85 weight percent 1-difluoromethoxy-1,2,2,2-tetrafluoroethane wherein said composition has a vapor pressure of about 17.5 psia at 25.degree. C.

2. An azeotropic or azeotrope-like composition consisting essentially of about 10 to about 99 weight percent 2,2,3,3-tetrafluorooxetane and about 1 to about 90 weight percent 1-difluoromethoxy-1,1,2,2-tetrafluoroethane wherein said composition has a vapor pressure of about 14 psia at 25.degree. C., or about 1 to about 60 weight percent 2,2,3,3-tetrafluorooxetane and about 40 to about 99 weight percent 1-difluoromethoxy-1,2,2,2-tetrafluoroethane wherein said composition has a vapor pressure of about 16 psia at 25.degree. C.

3. A process for producing refrigeration, comprising condensing a composition of claim 1, and thereafter evaporating said composition in the vicinity of the body to be cooled.

4. A process for producing refrigeration, comprising condensing a composition of claim 2, and thereafter evaporating said composition in the vicinity of the body to be cooled.

5. A process for producing heat comprising condensing a composition of claim 1 in the vicinity of a body to be heated, and thereafter evaporating said composition.

6. A process for producing heat comprising condensing a composition of claim 2, in the vicinity of a body to be heated, and thereafter evaporating said composition.