Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
  • C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
  • C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
  • C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
  • C08J9/143—Halogen containing compounds
  • C08J9/144—Halogen containing compounds containing carbon, halogen and hydrogen only
  • C08J9/146—Halogen containing compounds containing carbon, halogen and hydrogen only only fluorine as halogen atoms
• • 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
  • C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
  • C09K5/041—Materials 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
  • C09K5/044—Materials 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
  • C09K5/045—Materials 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
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2207/00—Foams characterised by their intended use
  • C08J2207/04—Aerosol, e.g. polyurethane foam spray
• • 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
  • C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
  • C09K2205/22—All components of a mixture being fluoro compounds

Definitions

• compositions that include at least two hydrofluorocarbons. These compositions are useful as refrigerants, cleaning agents, expansion agents for polyolefins and polyurethanes, aerosol propeUants, heat transfer media, gaseous dielectrics, fire extinguishing agents, power cycle working fluids, polymerization media, paniculate removal fluids, carrier fluids, buffing abrasive agents, and displacement drying agents.
• Fluorinated hydrocarbons have many uses, one of which is as a refrigerant.
• refrigerants include dichlorodifluoromethane (CFC-11) and chlorodifluoromethane (HCFC-22).
• HFCs Hydrofluorocarbons
• a refrigerant 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 to use as a refrigerant a single fluorinated hydrocarbon or an azeotropic or azeotrope-like composition that includes one or more fluorinated hydrocarbons.
• Fluorinated hydrocarbons may also be used as a cleaning agent or solvent to clean, for example, electronic circuit boards. It is desirable 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.
• Azeotropic or azeotrope-Uke compositions that include a fluorinated hydrocarbon are also useful as blowing agents in the manufacture of closed-cell polyurethane, phenohc and thermoplastic foams, as propeUants 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 poUshed 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.
• the present invention relates to the discovery of compositions of trifluoromethane (HFC-23) and pentafluoropropane; fluoromethane (HFC-41) and pentafluoropropane; tetrafluoroethane and heptafluoropropane or pentafluoropropane; 1,1-difluoroethane (HFC-152a) and heptafluoropropane, or pentafluoropropane; heptafluoropropane and pentafluoropropane, tetrafluoropropane, trifluoropropane, difluoropropane, or fiuoropropane; or 1,1,1,2,2,3,3-heptafluoropropane (HFC-227ca) and 1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea).
• compositions are useful as refrigerants, cleaning agents, expansion agents for polyolefins and polyurethanes, aerosol propeUants, heat transfer media, gaseous dielectrics, fire extinguishing agents, power cycle working fluids, polymerization media, paniculate removal fluids, carrier fluids, buffing abrasive agents, and displacement drying agents.
• the invention relates to the discovery of binary azeotropic or azeotrope-Uke compositions comprising effective amounts of these components to form an azeotropic or azeotrope-like composition.
• Figure 1 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-23 and HFC-245cb at 25°C;
• Figure 2 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-41 and HFC-245cb at 25°C;
• Figure 3 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-134a and HFC-227ca at 11.2°C
• Figure 4 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-134a and HFC-227ea at 11.2°C;
• Figure 5 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-134a and HFC-245cb at 25°C;
• Figure 6 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-152a and HFC-227ca at 11.2°C;
• Figure 7 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-152a and HFC-227ea at -10.0°C;
• Figure 8 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC- 152a and HFC-245cb at 25°C;
• Figure 9 is a graph of the vapor/Uquid eqmlibrium curve for mixtures of HFC-227ca and HFC-227ea at 25°C;
• Figure 10 is a graph of the vapor/liquid equiUbrium curve for mixtures of HFC-227ca and HFC-245cb at 25°C;
• Figure 11 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-227ca and HFC-263fb at 25°C;
• Figure 12 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-227ca and HFC-272ca at 25°C;
• Figure 13 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-227ca and HFC-281ea at 25°C;
• Figure 14 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-227ea and HFC-245cb at 25°C;
• Figure 15 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-227ea and HFC-245fa at 25°C;
• Figure 16 is a graph of the vapor/Uquid equiUbrium curve for mixtures of HFC-227ea and HFC-254cb at 25°C;
• Figure 17 is a graph of the vapor/Uquid equilibrium curve for mixtures of HFC-227ea and HFC-263fb at 25°C;
• Figure 18 is a graph of the vapor/liquid equiUbrium curve for mixtures of HFC-227ea and HFC-281ea at 25°C.
• the present invention relates to the following compositions: trifluoromethane (HFC-23) and pentafluoropropane; fluoromethane (HFC-41) and pentafluoropropane; tetrafluoroethane and heptafluoropropane or pentafluoropropane; 1,1-difluoroethane (HFC- 152a) and heptafluoropropane, or pentafluoropropane; heptafluoropropane and pentafluoropropane, tetrafluoropropane, trifluoropropane, difluoropropane, or fiuoropropane; or 1,1,1,2,2,3,3-heptafluoropropane (HFC-227ca) and 1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea).
• compositions include trifluoromethane (HFC-23) and 1,1,1,2,2-pentafluoropropane (HFC-245cb); fluoromethane (HFC-41) and 1,1,1,2,2- pentafluoropropane (HFC-245cb); 1,1,1,2-tetrafluoroethane (HFC- 134a), and 1, 1, 1,2,2,3,3-heptafluoropropane (HFC-227ca), 1, 1, 1,2,3,3,3-heptafluoropropane (HFC-227ea)or 1,1,1,2,2-pentafluoropropane (HFC-245cb); 1,1-difluoroethane (HFC- 152a) and 1,1,1,2,2,3,3-heptafluoropropane (HFC-227ca), 1,1,1,2,3,3,3- heptafluoropropane (HFC-227ea) or 1,1,1,2,2-pentafluoropropane (HFC-245
• the term "heptafluoropropane” includes 1,1,1,2,2,3,3-heptafluoropropane (HFC-227ca) and 1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea);
• the term "pentafluoropropane” includes 1,1,2,2,3-pentafluoropropane (HFC-245ca), 1,1,1,2,2-pentafluoropropane (HFC-245cb), 1,1,2,3,3- pentafluoropropane (HFC-245ea), 1,1,1,2,3-pentafluoropropane (HFC-245eb) and 1,1,1,3,3-pentafluoropropane (HFC-245fa);
• the term "tetrafluoropropane” includes 1,2,2,3-tetrafluoropropane (HFC-25
• the present invention also relates to the discovery of azeotropic or azeotrope-Uke compositions of effective amounts of HFC-23 and HFC-245cb; HFC-41 and HFC-245cb; HFC-134a and HFC-227ca, HFC-227ea or HFC-245cb; HFC-152a and HFC-227ca, HFC-227ea or HFC-245cb; HFC-227ca and HFC- 227ea, HFC-245cb, HFC-263fb, HFC-272ca, or HFC-281ea; or HFC-227ea and HFC-245cb, HFC-245fa, HFC-254cb, HFC-263fb or HFC-281ea to form an azeotropic or azeotrope-like composition.
• azeotropic composition is meant a constant boiling Uquid 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 distiUation of the Uquid has the same composition as the Uquid from which it was evaporated or distiUed, that is, the admixture distiUs/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.
• azeotrope-Uke composition is meant a constant boiling, or substantially constant boiling, Uquid admixture of two or more substances that behaves as a single substance.
• One way to characterize an azeotrope-Uke composition is that the vapor produced by partial evaporation or distiUation of the Uquid has substantially the same composition as the Uquid from which it was evaporated or distiUed, that is, the admixture distiUs/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.
• a composition is azeotrope-like if, after 50 weight percent of the composition is removed such as by evaporation or boi : ⁇ 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.
• 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.
• compositions that are azeotropic there is usually some range of compositions around the azeotrope point that, for a maximum boiUng azeotrope, have boiUng 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.
• 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.
• compositions of this invention have the foUowing vapor pressures at 25°C.
• SubstantiaUy constant boiling, azeotropic or azeotrope-like compositions of this invention comprise the following (all compositions are measured at 25°C):
• 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-Uke composition.
• This definition includes the amounts of each component, which amounts may vary depending on the pressure appUed to the composition so long as the azeotropic or azeotrope-Uke compositions continue to exist at the different pressures, but with possible different boiUng points.
• 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.
• azeotropic or constant-boiUng is intended to mean also essentially azeotropic or essentially-constant boiling.
• 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 weU as those equivalent compositions which are part of the same azeotropic system and are azeotrope-Uke in their properties.
• 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.
• azeotrope 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 wiU also change, at least to some degree, the boiling point temperature.
• 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.
• compositional ranges rather than fixed compositions, are often used to define azeotropes.
• 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 actuaUty, a series of such relationships, represented by A, B, C (and Denfin.) actually exist for a given azeotrope, varied by the influence of pressure.
• An azeotrope of A, B, C (and D%) can v ?e 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.
• a vessel is charged with an initial composition at 25°C, and the vapor pressure of the composition is measured.
• the composition is aUowed to leak from the vessel, whUe the temperature is held constant at 25°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.
• compositions of HFC-227ca and HFC-272ca are azeotropic or azeotrope-like at different temperatures, but that the weight percents of the components vary as the temperature is changed.
• EXAMPLE 4 Refrigerant Performance The foUowing table shows the performance of various refrigerants. The data are based on the foUowing conditions.
• 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.
• This Example is directed to measurements of the liquid/vapor equilibrium curves for the mixtures in Figures 1-2, 5, 8-18.
• the upper curve represents the composition of the Uquid
• the lower curve represents the composition of the vapor
• the data for the compositions of the Uquid in Figure 1 are obtained as foUows.
• a stainless steel cylinder is evacuated, and a weighed amount of HFC-23 is added to the cylinder.
• the cyUnder is cooled to reduce the vapor pressure of HFC- 23, and then a weighed amount of HFC-245cb is added to the cylinder.
• the cylinder is agitated to mix the HFC-23 and HFC-245cb, and then the cyUnder is placed in a constant temperature bath until the temperature comes to equilibrium at 25°C, at which time the vapor pressure of the HFC-23 and HFC-245cb in the cylinder is measured. Additional samples of Uquid are measured the same way, and the results are plotted in Figure 1.
• the curve which shows the composition of the vapor is calculated using an ideal gas equation of state.
• Vapor/liquid equiUbrium data are obtained in the same way for the mixtures shown in Figures 2, 5, 8-18.
• EXAMPLE 6 This Example is directed to measurements of the liquid/vapor equiUbrium curve for mixtures of HFC-134a/HFC-227ca; HFC-134a/HFC-227ea; HFC-152a/HFC-227ca and HFC-152a/HFC-227ea.
• the Uquid/vapor equiUbrium data for these mixtures are shown in Figures 3, 4, 6 and 7.
• the upper curve represents the Uquid composition
• the lower curve represents the vapor composition.
• the procedure for measuring the composition of the Uquid for mixtures of HFC-134a/HFC-227ca in Figure 3 was as foUows.
• a stainless steel cylinder was evacuated, and a weighed amount of HFC-134a was added to the cylinder.
• the cylinder was cooled to reduce the vapor pressure of HFC- 134a, and then a weighed amount of HFC-227ca was added to the cylinder.
• the cyUnder was agitated to mix the HFC-134a/HFC-227ca, and then the cylinder was placed in a constant temperature bath until the temperature came to equiUbrium at 11.2°C, at which time the vapor pressure of the content of the cyUnder was measured.
• the data in Figure 6 show that at 11.2°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 may result in an unexpected increase in the refrigeration capacity or efficiency of those compositions when compared to the pure components of the compositions.
• the data in Figures 3, 4 and 7 show that although those compositions do not exhibit a maximum or minimum vapor pressure at a particular temperature, they are substantiaUy constant boiling compositions, that is azeotrope-like compositions, because the compositions have dew point vapor pressures and bubble point vapor pressures that are substantially the same at a particular temperature.
• novel compositions of this invention may be used to produce refrigeration by condensing the compositions and thereafter evaporating the condensate in the vicinity of a body to be cooled.
• the novel 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.
• novel compositions of the invention are particularly suitable for replacing refrigerants that may affect the ozone layer, including R-ll, R-12, R-22, R-114 and R-502.
• novel constant boiling or substantially constant boiling compositions of the invention are also useful as aerosol propeUants, 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 aUphatic hydrocarbons having a boiling point of -60 to + 60°C, hydrofluorocarbonalkanes having a boiling point of -60 to + 60°C, hydrofluoropropanes having a boiling point of between -60 to + 60°C, hydrocarbon esters having a boiling point between -60 to + 60°C, hydrochlorofluorocarbons having a boiling point between -60 to + 60°C, hydrofluorocarbons having a boiling point of -60 to + 60°C, hydrochlorocarbons having a boiling point between -60 to +60°C, chlorocarbons and perfluorinated compounds, can be added to the azeotropic or azeotrope-like compositions described above without substantiaUy 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 appUcation.
• Preferred lubricants include esters having a molecular weight greater than 250.

Landscapes

• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Chemistry (AREA)
• Combustion & Propulsion (AREA)
• Thermal Sciences (AREA)
• Physics & Mathematics (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Detergent Compositions (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Applications Claiming Priority (5)

Publications (1)

Family

ID=26823010

Family Applications (1)

Country Status (5)

Families Citing this family (21)

Family Cites Families (7)

• 1994
  • 1994-08-17 TW TW83107553A patent/TW283164B/zh active
  • 1994-09-21 JP JP7509826A patent/JPH09503204A/ja not_active Withdrawn
  • 1994-09-21 WO PCT/US1994/010341 patent/WO1995008603A1/en not_active Application Discontinuation
  • 1994-09-21 AU AU77964/94A patent/AU7796494A/en not_active Abandoned
  • 1994-09-21 EP EP94928582A patent/EP0720640A1/de not_active Withdrawn

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events