US20110197602A1 - Heat transfer method - Google Patents
Heat transfer method Download PDFInfo
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- US20110197602A1 US20110197602A1 US13/122,890 US200913122890A US2011197602A1 US 20110197602 A1 US20110197602 A1 US 20110197602A1 US 200913122890 A US200913122890 A US 200913122890A US 2011197602 A1 US2011197602 A1 US 2011197602A1
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- refrigerant fluid
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- 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
-
- 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
- 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
- C09K2205/10—Components
- C09K2205/12—Hydrocarbons
- C09K2205/122—Halogenated hydrocarbons
-
- 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
- C09K2205/10—Components
- C09K2205/12—Hydrocarbons
- C09K2205/126—Unsaturated fluorinated hydrocarbons
Definitions
- the present invention relates to a heat transfer process using a composition containing hydrochlorofluoroolefins. It relates more particularly to the use of a composition containing hydrochlorofluoroolefins in heat pumps.
- HFC-134a Hydrofluorocarbon (1,1,1,2-tetrafluoroethane: HFC-134a) refrigerant fluid which is less harmful to the ozone layer.
- CFC-12 chlorofluorocarbon
- HFC-134a hydrofluorocarbon (1,1,1,2-tetrafluoroethane: HFC-134a) refrigerant fluid which is less harmful to the ozone layer.
- the contribution to the greenhouse effect of a fluid is quantified by a criterion, the GWP (Global Warming Potential), which indexes the warming potential by taking a reference value of 1 for carbon dioxide.
- carbon dioxide is non-toxic and non-flammable and has a very low GWP
- it has been proposed as a refrigerant fluid for air conditioning systems as a replacement for HFC-134a.
- carbon dioxide there are several disadvantages to the use of carbon dioxide, related in particular to the very high pressure of the use thereof as a refrigerant fluid in existing devices and technologies.
- compositions comprising at least one fluoroalkene having three or four carbon atoms, in particular pentafluoropropene and tetrafluoropropene, preferably having a GWP at most of 150, as heat transfer fluids.
- fluorohaloalkenes having from to 6 carbon atoms in particular tetrafluoropropenes, pentafluoropropenes and chlorotrifluoropropenes, have been described as capable of being used as a heat transfer fluid.
- compositions containing hydrochlorofluoroolefins are very particularly suitable as heat transfer fluid in heat pumps, in particular heat pumps that operate at a high condensing temperature. Moreover, these compositions have a negligible ODP and a GWP below that of existing heat transfer fluids.
- hydrofluoroolefins is understood to mean olefins having from 3 to 4 carbon atoms that comprise one chlorine atom and at least one fluorine atom.
- the chlorine atom is borne by the unsaturated carbon.
- a heat pump is a thermodynamic device allowing the transfer of heat from the coldest medium to the hottest medium.
- the heat pumps used for heating are referred to as compression heat pumps and the operation is based on the principle of the compression cycle of fluids, referred to as refrigerant fluids.
- These heat pumps operate with compression systems comprising a single or several stage(s). At a given stage, when the refrigerant fluid is compressed and passes from the gaseous state to the liquid state, an exothermic reaction (condensation) takes place that produces heat. Conversely, if the fluid is expanded by passing it from the liquid state to the gaseous state, an endothermic reaction (evaporation) takes place, which produces a cold sensation. Everything therefore relies on the change of state of a fluid used in a closed circuit.
- Each stage of a compression system comprises (i) a step of evaporation during which, in contact with heat drawn from the surroundings, the refrigerant fluid, by virtue of its low boiling point, changes from the liquid state to the gaseous state, (ii) a step of compression during which the gas from the preceding step is brought to high pressure, (iii) a step of condensation during which the gas will transmit its heat to the heating circuit; the refrigerant, still compressed, becomes liquid again and (iv) a step of expansion during which the pressure of the fluid is reduced.
- the fluid is ready for a new absorption of heat from the cold environment.
- One subject of the present invention is a heat transfer process using a compression system having at least one stage successively comprising a step of evaporation of a refrigerant fluid, a step of compression, a step of condensation of said fluid at a temperature greater than or equal to 70° C. and a step of expansion of said fluid characterized in that the refrigerant fluid comprises at least one hydrochlorofluoroolefin.
- the condensing temperature of the refrigerant fluid is between 70 and 140° C., and advantageously between 95 and 125° C.
- the hydrochlorofluoroolefins comprise at least three fluorine atoms.
- hydrochlorofluoroolefins are chlorotrifluoropropenes (HCFO-1233), in particular 1-chloro-3,3,3-trifluoropropene (HCFO-1233zd) and 2-chloro-3,3,3-trifluoropropene (HCFO-1233xf).
- HCFO-1233 chlorotrifluoropropenes
- HCFO-1233zd 1-chloro-3,3,3-trifluoropropene
- 2-chloro-3,3,3-trifluoropropene HCFO-1233xf
- the 1-chloro-3,3,3-trifluoropropene may be in either cis form or trans form.
- the refrigerant fluid may comprise at least one hydrofluorocarbon.
- hydrofluorocarbons mention may especially be made of 1,1,1,3,3-pentafluorobutane, 1,1,1,2-tetrafluoroethane, pentafluoroethane, 1,1,1,3,3-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, 1,1,1,2,2-penta-fluoropropane and 1,1,1,2,3,3,3-heptafluoropropane.
- the refrigerant fluid may also comprise at least one fluoroether, preferably at least one hydrofluoroether and advantageously at least one hydrofluoroether having from three to six carbon atoms.
- hydrofluoroethers mention may especially be made of heptafluoromethoxypropane, nonafluoromethoxybutane and nonafluoroethoxybutane.
- the hydrofluoroether is available in several isomeric forms such as 1,1,1,2,2,3,3,4,4-nonafluoroethoxybutane, 1,1,1,2,3,3-hexafluoro-2-(trifluoromethyl)-3-ethoxybutane, 1,1,1,2,2,3,3,4,4-nonafluoromethoxybutane and 1,1,1,2,3,3-hexafluoro-2-(trifluoromethyl)-3-methoxybutane.
- the refrigerant fluid may also comprise at least one fluoroalkene having from 3 to 6 carbon atoms.
- the fluoroalkene is chosen from fluoropropenes, in particular trifluoropropenes such as 1,1,1-trifluoropropene, tetrafluoropropenes such as 2,3,3,3-tetrafluoropropene (HFO-1234yf), 1,3,3,3-tetrafluoropropene and fluorobutenes. Fluoromethyl-propenes may be suitable.
- the refrigerant fluid comprises at least 10% by weight of hydrochlorofluoroolefins.
- the refrigerant fluid used in the present invention may comprise a stabilizer of the hydrochlorofluoroolefin.
- the stabilizer represents at most 5% by weight relative to the total composition of the fluid.
- nitromethane ascorbic acid, terephthalic acid, azoles such as tolutriazole or benzotriazole, phenolic compounds such as tocopherol, hydroquinone, t-butylhydroguinone, 2,6-di-cert-butyl-4-methylphenol, epoxides (alkyl, optionally fluorinated or perfluorinated, or alkenyl or aromatic epoxides) such as n-butyl glycidyl ether, hexanediol diglycidyl ether, allyl glycidyl ether or butylphenyl glycidyl ether, phosphites, phosphates, phosphonates, thiols and lactones.
- epoxides alkyl, optionally fluorinated or perfluorinated, or alkenyl or aromatic epoxides
- the refrigerant used in the process according to the present invention may comprise lubricants such as mineral oil, alkylbenzene, polyalkylene glycol and polyvinyl ether.
- Evap P is the pressure at the evaporator
- Cond P is the pressure at the condenser
- T cond is the condensing temperature
- Te comp is the compressor inlet temperature
- T outlet comp is the compressor outlet temperature
- COP coefficient of performance and is defined, where a heat pump is concerned, as being the useful heat power provided the system over the power taken in or consumed by the system
- % CAP or COP is the ratio of the value of the CAP or COP of the fluid relative to that obtained with HCFC-114.
- the nominal operating pressure is 14.19 bar
- the volumetric capacity is 785 kJ/m 3
- the COP is 2.07 under the following operating conditions:
- the nominal operating pressure is 9.3 bar
- the volumetric capacity is 3321 kJ/m 3
- the COP is 8.19 under the following operating conditions:
- the nominal operating pressure is 12.82 bar
- the volumetric capacity is 2976 kJ/m 3
- the COP is 5.19 under the following operating conditions:
- the nominal operating pressure is 17.26 bar
- the volumetric capacity is 2573 kJ/m 3
- the COP is 3.56 under the following operating conditions:
- the nominal operating pressure is 20.82 bar
- the volumetric capacity is 2257 kJ/m 3
- the COP is 2.79 under the following operating conditions:
- the nominal operating pressure is 17.26 bar
- the volumetric capacity is 5475 kJ/m 3
- the COP is 7.94 under the following operating conditions:
- the nominal operating pressure is 20.82 bar
- the volumetric capacity is 4810 kJ/m 3
- the COP is 5.45 under the following operating conditions:
- the nominal operating pressure is 24.92 bar
- the volumetric capacity is 4027 kJ/m 3
- the COP is 3.79 under the following operating conditions:
- the nominal operating pressure is 29.61 bar
- the volumetric capacity is 2971 kJ/m 3
- the COP is 2.46 under the following operating conditions:
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- Engineering & Computer Science (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
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- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The present invention relates to a method of heat transfer by means of a composition containing hydrochlorofluoroolefins. The subject matter of the present invention is more particularly a heat transfer method comprising, successively, a step of evaporation of a coolant fluid, a compression step, a step of condensation of said fluid at a temperature of greater than or equal to 70° C. and a step of expansion of said fluid, characterized in that that coolant fluid comprises at least one hydrochlorofluoroolefin.
Description
- The present invention relates to a heat transfer process using a composition containing hydrochlorofluoroolefins. It relates more particularly to the use of a composition containing hydrochlorofluoroolefins in heat pumps.
- The problems posed by substances which deplete the atmospheric ozone layer (ODP: ozone depletion potential) were tackled at Montreal, where the protocol imposing a reduction in the production and use of chlorofluorocarbons (CFCs) was signed. This protocol has been the subject of amendments which have required that CFCs be withdrawn and have extended regulatory control to other products.
- The refrigeration industry and the air conditioning industry have invested a great deal in the replacement of these refrigerant fluids.
- In the automotive industry, the air conditioning systems for vehicles sold in many countries have changed from a chlorofluorocarbon (CFC-12) refrigerant fluid to a hydrofluorocarbon (1,1,1,2-tetrafluoroethane: HFC-134a) refrigerant fluid which is less harmful to the ozone layer. However, from the viewpoint of the objectives set by the Kyoto protocol, HFC-134a (GWP=1300) is regarded as having a high warming potential. The contribution to the greenhouse effect of a fluid is quantified by a criterion, the GWP (Global Warming Potential), which indexes the warming potential by taking a reference value of 1 for carbon dioxide.
- As carbon dioxide is non-toxic and non-flammable and has a very low GWP, it has been proposed as a refrigerant fluid for air conditioning systems as a replacement for HFC-134a. However, there are several disadvantages to the use of carbon dioxide, related in particular to the very high pressure of the use thereof as a refrigerant fluid in existing devices and technologies.
- Document JP 4110388 describes the use of hydro-fluoropropenes of formula C3HmFn with m and n representing an integer between 1 and 5 inclusive and m+n=6, as heat transfer fluids, in particular tetrafluoropropene and trifluoropropene.
- Document WO 2004/037913 discloses the use of compositions comprising at least one fluoroalkene having three or four carbon atoms, in particular pentafluoropropene and tetrafluoropropene, preferably having a GWP at most of 150, as heat transfer fluids.
- In document WO 2007/002625, fluorohaloalkenes having from to 6 carbon atoms, in particular tetrafluoropropenes, pentafluoropropenes and chlorotrifluoropropenes, have been described as capable of being used as a heat transfer fluid.
- In the field of heat pumps, substitutes for dichlorotetrafluoroethane (HCFC-114), used under conditions of high condensing temperature, have been proposed. Thus, document U.S. Pat. No. 6,814,884 describes a composition comprising 1,1,1,3,3-pentafluorobutane (HFC-365mfc) and at least one compound chosen from 1,1,1,2-tetrafluoroethane, pentafluoroethane (HFC-125), 1,1,1,3,3-pentafluoropropane (HFC-245fa) and 1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea). However, these compounds have a high GWP.
- The applicant has now discovered that compositions containing hydrochlorofluoroolefins are very particularly suitable as heat transfer fluid in heat pumps, in particular heat pumps that operate at a high condensing temperature. Moreover, these compositions have a negligible ODP and a GWP below that of existing heat transfer fluids.
- The term “hydrochlorofluoroolefins” is understood to mean olefins having from 3 to 4 carbon atoms that comprise one chlorine atom and at least one fluorine atom. Preferably, the chlorine atom is borne by the unsaturated carbon.
- A heat pump is a thermodynamic device allowing the transfer of heat from the coldest medium to the hottest medium. The heat pumps used for heating are referred to as compression heat pumps and the operation is based on the principle of the compression cycle of fluids, referred to as refrigerant fluids. These heat pumps operate with compression systems comprising a single or several stage(s). At a given stage, when the refrigerant fluid is compressed and passes from the gaseous state to the liquid state, an exothermic reaction (condensation) takes place that produces heat. Conversely, if the fluid is expanded by passing it from the liquid state to the gaseous state, an endothermic reaction (evaporation) takes place, which produces a cold sensation. Everything therefore relies on the change of state of a fluid used in a closed circuit.
- Each stage of a compression system comprises (i) a step of evaporation during which, in contact with heat drawn from the surroundings, the refrigerant fluid, by virtue of its low boiling point, changes from the liquid state to the gaseous state, (ii) a step of compression during which the gas from the preceding step is brought to high pressure, (iii) a step of condensation during which the gas will transmit its heat to the heating circuit; the refrigerant, still compressed, becomes liquid again and (iv) a step of expansion during which the pressure of the fluid is reduced. The fluid is ready for a new absorption of heat from the cold environment.
- One subject of the present invention is a heat transfer process using a compression system having at least one stage successively comprising a step of evaporation of a refrigerant fluid, a step of compression, a step of condensation of said fluid at a temperature greater than or equal to 70° C. and a step of expansion of said fluid characterized in that the refrigerant fluid comprises at least one hydrochlorofluoroolefin.
- Preferably, the condensing temperature of the refrigerant fluid is between 70 and 140° C., and advantageously between 95 and 125° C.
- Preferably, the hydrochlorofluoroolefins comprise at least three fluorine atoms.
- Particularly advantageous hydrochlorofluoroolefins are chlorotrifluoropropenes (HCFO-1233), in particular 1-chloro-3,3,3-trifluoropropene (HCFO-1233zd) and 2-chloro-3,3,3-trifluoropropene (HCFO-1233xf). The 1-chloro-3,3,3-trifluoropropene may be in either cis form or trans form.
- Besides the hydrochlorofluoroolefin(s), the refrigerant fluid may comprise at least one hydrofluorocarbon.
- As hydrofluorocarbons, mention may especially be made of 1,1,1,3,3-pentafluorobutane, 1,1,1,2-tetrafluoroethane, pentafluoroethane, 1,1,1,3,3-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, 1,1,1,2,2-penta-fluoropropane and 1,1,1,2,3,3,3-heptafluoropropane.
- The refrigerant fluid may also comprise at least one fluoroether, preferably at least one hydrofluoroether and advantageously at least one hydrofluoroether having from three to six carbon atoms.
- As hydrofluoroethers, mention may especially be made of heptafluoromethoxypropane, nonafluoromethoxybutane and nonafluoroethoxybutane. The hydrofluoroether is available in several isomeric forms such as 1,1,1,2,2,3,3,4,4-nonafluoroethoxybutane, 1,1,1,2,3,3-hexafluoro-2-(trifluoromethyl)-3-ethoxybutane, 1,1,1,2,2,3,3,4,4-nonafluoromethoxybutane and 1,1,1,2,3,3-hexafluoro-2-(trifluoromethyl)-3-methoxybutane.
- The refrigerant fluid may also comprise at least one fluoroalkene having from 3 to 6 carbon atoms. Preferably, the fluoroalkene is chosen from fluoropropenes, in particular trifluoropropenes such as 1,1,1-trifluoropropene, tetrafluoropropenes such as 2,3,3,3-tetrafluoropropene (HFO-1234yf), 1,3,3,3-tetrafluoropropene and fluorobutenes. Fluoromethyl-propenes may be suitable.
- Preferably, the refrigerant fluid comprises at least 10% by weight of hydrochlorofluoroolefins.
- The refrigerant fluid used in the present invention may comprise a stabilizer of the hydrochlorofluoroolefin. The stabilizer represents at most 5% by weight relative to the total composition of the fluid.
- As stabilizers, mention may especially be made of nitromethane, ascorbic acid, terephthalic acid, azoles such as tolutriazole or benzotriazole, phenolic compounds such as tocopherol, hydroquinone, t-butylhydroguinone, 2,6-di-cert-butyl-4-methylphenol, epoxides (alkyl, optionally fluorinated or perfluorinated, or alkenyl or aromatic epoxides) such as n-butyl glycidyl ether, hexanediol diglycidyl ether, allyl glycidyl ether or butylphenyl glycidyl ether, phosphites, phosphates, phosphonates, thiols and lactones.
- The refrigerant used in the process according to the present invention may comprise lubricants such as mineral oil, alkylbenzene, polyalkylene glycol and polyvinyl ether.
- In what follows:
- Evap P is the pressure at the evaporator
- Cond P is the pressure at the condenser
- T cond is the condensing temperature
- Te comp is the compressor inlet temperature
- Ratio: the compression ratio
- T outlet comp is the compressor outlet temperature
- COP: coefficient of performance and is defined, where a heat pump is concerned, as being the useful heat power provided the system over the power taken in or consumed by the system
- CAP: volumetric capacity, heat capacity per unit volume (kJ/m3)
- % CAP or COP is the ratio of the value of the CAP or COP of the fluid relative to that obtained with HCFC-114.
- The performances of the refrigerant fluid under the heat pump operating conditions and by setting the temperature at the evaporator to 10° C. and that at the condenser to 100° C. are given below.
- For HCFC-114, the nominal operating pressure is 14.19 bar, the volumetric capacity is 785 kJ/m3 and the COP is 2.07 under the following operating conditions:
- Isentropic efficiency of the compressor: 80%
-
HFC-365mfc/ HCFC-114 HFC-365mfc HCFO-1233zd HFC-227ea Temp evap 10 10 10 10 (° C.) T e comp 15 15 15 15 Evap P (kPa) 129 30 76 Cond P (kPa) 1419 590 1048 Ratio (p/p) 11.04 19.81 13.72 27.1 T cond (° C.) 100 100 100 100 T outlet 100 100 103 comp (° C.) CAP (kJ/m3) 785 260 630 374 COP 2.07 2.30 2.42 2.40 % CAP 100 33 80 48 % COP 100 111 117 116 - The performances of the refrigerant fluid under the heat pump operating conditions and by setting the temperature at the evaporator to 50° C. and that at the condenser to 80° C. are given below.
- For HCFC-114, the nominal operating pressure is 9.3 bar, the volumetric capacity is 3321 kJ/m3 and the COP is 8.19 under the following operating conditions:
- Isentropic efficiency of the compressor: 80%
-
HCFC-114 HFC-365mfc HCFO-1233zd Temp outlet evap (° C.) 50 50 50 T e comp (° C.) 65 65 65 Evap P (kPa) 447 142 298 Cond P (kPa) 930 352 663 Ratio(p/p) 2.08 2.48 2.22 T cond (° C.) 80 80 80 T outlet comp (° C.) 90 87 94 CAP (kJ/m3) 3321 1394 2554 COP 8.19 8.60 8.53 % CAP 100 42 77 % COP 100 105 104 - The performances of the refrigerant fluid under the heat pump operating conditions and by setting the temperature at the evaporator to 50° C. and the temperature at the condenser to 95° C. are given below.
- For HCFC-114, the nominal operating pressure is 12.82 bar, the volumetric capacity is 2976 kJ/m3 and the COP is 5.19 under the following operating conditions:
- Isentropic efficiency of the compressor: 80%
-
HCFC- HFC- HCFO- HFO- 114 365mfc 1233zd 1234yf Temp evap (° C.) 50 50 50 50 T e comp (° C.) 65 65 65 65 Evap P (kPa) 447 142 298 1283 Cond P (kPa) 1282 522 939 3345 Ratio (p/p) 2.87 3.67 3.15 2.61 T cond (° C) 95 95 95 95 T outlet comp (° C.) 103 98 107 113 CAP (kJ/m3) 2976 1284 2379 4065 COP 5.19 5.56 5.56 2.80 % CAP 100 43 80 137 % COP 100 107 107 54 - The performances of the refrigerant fluid under the heat pump operating conditions and by setting the temperature at the evaporator to 50° C. and that at the condenser to 110° C. are given below.
- For HCFC-114, the nominal operating pressure is 17.26 bar, the volumetric capacity is 2573 kJ/m3 and the COP is 3.56 under the following operating conditions:
- Isentropic efficiency of the compressor: 80%
-
HCFC-114 HFC-365mfc HCFO-1233zd Temp evap (° C.) 50 50 50 T e comp (° C.) 65 65 65 Evap P (kPa) 447 142 298 Cond P (kPa) 1726 748 1294 Ratio (p/p) 3.86 5.26 4.34 T cond (° C.) 110 110 110 T outlet comp (° C.) 116 110 121 CAP (kJ/m3) 2573 1157 2172 COP 3.56 3.97 4.00 % CAP 100 45 84 % COP 100 111 112 - The performances of the refrigerant fluid under the heat pump operating conditions and by setting the temperature at the evaporator to 50° C. and that at the condenser to 120° C. are given below.
- For HCFC-114, the nominal operating pressure is 20.82 bar, the volumetric capacity is 2257 kJ/m3 and the COP is 2.79 under the following operating conditions:
- Isentropic efficiency of the compressor: 80%
-
HCFC-114 HFC-365mfc HCFO-1233zd Temp evap (° C.) 50 50 50 T e comp 65 65 65 Evap P (kPa) 447 142 298 Cond P (kPa) 2082 936 1581 Ratio (p/p) 4.66 6.58 5.30 T cond (° C.) 120 120 120 T outlet comp (° C.) 125 120 130 CAP (kJ/m3) 2257 1063 2015 COP 2.79 3.25 3.29 % CAP 100 47 89 % COP 100 116 118 - The performances of the refrigerant fluid under the heat pump operating conditions and by setting the temperature at the evaporator to 80° C. and that at the condenser to 110° C. are given below.
- For HCFC-114, the nominal operating pressure is 17.26 bar, the volumetric capacity is 5475 kJ/m3 and the COP is 7.94 under the following operating conditions:
- Isentropic efficiency of the compressor: 80%
-
HCFC-114 HFC-365mfc HCFO-1233zd Temp evap (° C.) 80 80 80 T e comp (° C.) 90 90 90 Evap P (kPa) 930 352 663 Cond P (kPa) 1726 748 1294 Ratio (p/p) 1.86 2.12 1.95 T cond (° C.) 110 110 110 T outlet comp (° C.) 116 111 117 CAP (kJ/m3) 5475 2872 4705 COP 7.94 8.83 8.72 % CAP 100 52 86 % COP 100 111 110 - The performances of the refrigerant fluid under the heat pump operating conditions and by setting the temperature at the evaporator to 80° C. and that at the condenser to 120° C. are given below.
- For HCFC-114, the nominal operating pressure is 20.82 bar, the volumetric capacity is 4810 kJ/m3 and the COP is 5.45 under the following operating conditions:
- Isentropic efficiency of the compressor: 80%
-
HCFC-114 HFC-365mfc HCFO-1233zd Temp evap (° C.) 80 80 80 T e comp (° C.) 90 90 90 Evap P (kPa) 930 352 663 Cond P (kPa) 2082 936 1581 Ratio (p/p) 2.24 2.66 2.38 T cond (° C.) 120 120 120 T outlet comp (° C.) 126 120 127 CAP (kJ/m3) 4810 2648 4360 COP 5.45 6.36 6.24 % CAP 100 55 91 % COP 100 117 114 - The performances of the refrigerant fluid under the heat pump operating conditions and by setting the temperature at the evaporator to 80° C. and that at the condenser to 130° C. are given below.
- For HCFC-114, the nominal operating pressure is 24.92 bar, the volumetric capacity is 4027 kJ/m3 and the COP is 3.79 under the following operating conditions:
- Isentropic efficiency of the compressor: 80%
-
HCFC-114 HFC-365mfc HCFO-1233zd Temp evap (° C.) 80 80 80 T e comp (° C.) 90 90 90 Evap P (kPa) 930 352 663 Cond P (kPa) 2492 1157 1913 Ratio (p/p) 2.68 3.28 2.88 T cond (° C.) 130 130 130 T outlet comp (° C.) 136 130 136 CAP (kJ/m3) 4027 2403 3967 COP 3.79 4.81 4.71 % CAP 100 60 99 % COP 100 127 124 - The performances of the refrigerant fluid under the heat pump operating conditions and by setting the temperature at the evaporator to 80° C. and that at the condenser to 140° C. are given below.
- For HCFC-114, the nominal operating pressure is 29.61 bar, the volumetric capacity is 2971 kJ/m3 and the COP is 2.46 under the following operating conditions:
- Isentropic efficiency of the compressor: 80%
-
HCFC-114 HFC-365mfc HCFO-1233zd Temp evap (° C.) 80 80 80 T e comp (° C.) 90 90 90 Evap P (kPa) 930 352 663 Cond P (kPa) 2961 1417 2295 Ratio (p/p) 3.19 4.02 3.46 T cond (° C.) 140 140 140 T outlet comp (° C.) 147 140 147 CAP (kJ/m3) 2971 2134 3520 COP 2.46 3.73 3.62 % CAP 100 72 118 % COP 100 152 147
Claims (8)
1. A heat transfer process using a compression system comprising successively a step of evaporation of a refrigerant fluid, a step of compression of said refrigerant fluid, a step of condensation of said refrigerant fluid at a temperature greater than or equal to 70° C. and a step of expansion of said refrigerant fluid characterized in that the refrigerant fluid comprises at least one hydrochlorofluoroolefin.
2. The process as claimed in claim 1 , characterized in that the temperature is between 70 and 140° C.
3. The process as claimed in claim 1 , characterized in that the refrigerant fluid comprises at least one hydrofluorocarbon.
4. The process as claimed in claim 1 , characterized in that the refrigerant fluid comprises at least one hydrofluoroether.
5. The process as claimed in claim 1 , characterized in that the refrigerant fluid comprises at least one fluoroalkene.
6. The process as claimed in claim 1 , characterized in that the hydrochlorofluoroolefin comprises at least three fluorine atoms.
7. The process as claimed in claim 1 , characterized in that the hydrochlorofluoroolefin is selected from the group consisting of 1-chloro-3,3,3-trifluoropropene and 2-chloro-3,3,3 -trifluoropropene.
8. The process as claimed in claim 1 , characterized in that the temperature is between 95 and 125° C.
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FR0857032 | 2008-10-16 | ||
FR0857032A FR2937328B1 (en) | 2008-10-16 | 2008-10-16 | HEAT TRANSFER METHOD |
PCT/FR2009/051943 WO2010043807A1 (en) | 2008-10-16 | 2009-10-13 | Heat transfer method |
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PCT/FR2009/051943 A-371-Of-International WO2010043807A1 (en) | 2008-10-16 | 2009-10-13 | Heat transfer method |
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US16/027,743 Continuation US10858561B2 (en) | 2008-10-16 | 2018-07-05 | Heat transfer method |
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US20110197602A1 true US20110197602A1 (en) | 2011-08-18 |
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US13/122,890 Abandoned US20110197602A1 (en) | 2008-10-16 | 2009-10-13 | Heat transfer method |
US16/027,743 Active US10858561B2 (en) | 2008-10-16 | 2018-07-05 | Heat transfer method |
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US16/027,743 Active US10858561B2 (en) | 2008-10-16 | 2018-07-05 | Heat transfer method |
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US (2) | US20110197602A1 (en) |
EP (1) | EP2334750B1 (en) |
JP (2) | JP6077744B2 (en) |
CN (2) | CN106244112B (en) |
ES (1) | ES2668968T3 (en) |
FR (1) | FR2937328B1 (en) |
HU (1) | HUE037538T2 (en) |
PL (1) | PL2334750T3 (en) |
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- 2009-10-13 PT PT97560106T patent/PT2334750T/en unknown
- 2009-10-13 CN CN201610607752.3A patent/CN106244112B/en active Active
- 2009-10-13 CN CN2009801400780A patent/CN102177215A/en active Pending
- 2009-10-13 PL PL09756010T patent/PL2334750T3/en unknown
- 2009-10-13 JP JP2011531537A patent/JP6077744B2/en active Active
- 2009-10-13 EP EP09756010.6A patent/EP2334750B1/en active Active
- 2009-10-13 ES ES09756010.6T patent/ES2668968T3/en active Active
- 2009-10-13 US US13/122,890 patent/US20110197602A1/en not_active Abandoned
- 2009-10-13 HU HUE09756010A patent/HUE037538T2/en unknown
- 2009-10-13 WO PCT/FR2009/051943 patent/WO2010043807A1/en active Application Filing
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2015
- 2015-02-13 JP JP2015026010A patent/JP6151731B2/en active Active
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2018
- 2018-07-05 US US16/027,743 patent/US10858561B2/en active Active
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US10858561B2 (en) | 2008-10-16 | 2020-12-08 | Arkema France | Heat transfer method |
US20120329893A1 (en) * | 2010-03-09 | 2012-12-27 | Arkema France | Hydrochlorofluoroolefin blowing agent compositions |
US10662357B2 (en) | 2010-07-09 | 2020-05-26 | Arkema France | Stable 2,3,3,3-tetrafluoropropene composition |
US10119055B2 (en) | 2010-07-09 | 2018-11-06 | Arkema France | Stable 2,3,3,3-tetrafluoropropene composition |
US9807994B2 (en) * | 2011-01-25 | 2017-11-07 | Technologies Holdings Corp. | Portable heating system and method for pest control |
US9578867B2 (en) | 2011-01-25 | 2017-02-28 | Technologies Holding Corp. | Portable heating system and method for pest control |
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US20140144066A1 (en) * | 2011-01-25 | 2014-05-29 | Technologies Holdings Corp. | Portable heating system and method for pest control |
US20170101568A1 (en) * | 2011-05-19 | 2017-04-13 | Asahi Glass Company, Limited | Working medium and heat cycle system |
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US10343963B2 (en) | 2013-03-20 | 2019-07-09 | Arkema France | Composition comprising HF and E-3,3,3-trifluoro-1-chloropropene |
US10077221B2 (en) | 2013-03-20 | 2018-09-18 | Arkema France | Composition comprising HF and E-3,3,3-trifluoro-1-chloropropene |
US10215455B2 (en) | 2013-08-14 | 2019-02-26 | Central Glass Company, Limited | Heat transmission method and high-temperature heat pump device |
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US10532965B2 (en) | 2014-01-13 | 2020-01-14 | Arkema France | E-1-chloro-3,3,3-trifluoropropene production process from 1,1,3,3-tetrachloropropene |
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US10399918B2 (en) | 2015-03-18 | 2019-09-03 | Arkema France | Stabilization of 1-chloro-3,3,3-trifluoropropene |
US10618861B2 (en) | 2015-03-18 | 2020-04-14 | Arkema France | Stabilization of 1-chloro-3,3,3-trifluoropropene |
US20160272561A1 (en) * | 2015-03-18 | 2016-09-22 | Arkema France | Stabilization of 1-chloro-3,3,3-trifluoropropene |
US10988422B2 (en) | 2015-05-21 | 2021-04-27 | The Chemours Company Fc, Llc | Hydrofluoroalkane composition |
US10301236B2 (en) | 2015-05-21 | 2019-05-28 | The Chemours Company Fc, Llc | Hydrofluorination of a halogenated olefin with SbF5 in the liquid phase |
US11008267B2 (en) | 2015-05-21 | 2021-05-18 | The Chemours Company Fc, Llc | Hydrofluoroalkane composition |
US11572326B2 (en) | 2015-05-21 | 2023-02-07 | The Chemours Company Fc, Llc | Method for preparing 1,1,1,2,2-pentafluoropropane |
US12006274B2 (en) | 2015-05-21 | 2024-06-11 | The Chemours Company Fc, Llc | Compositions including olefin and hydrofluoroalkane |
US10427998B2 (en) | 2015-05-22 | 2019-10-01 | Arkema France | Compositions based on 1,1,3,3-tetrachloropropene |
US10669465B2 (en) | 2016-09-19 | 2020-06-02 | Arkema France | Composition comprising 1-chloro-3,3,3-trifluoropropene |
US11053420B2 (en) | 2017-09-12 | 2021-07-06 | Arkema France | Composition on the basis of hydrochlorofluoroolefin and mineral oil |
US11242304B2 (en) | 2018-05-16 | 2022-02-08 | Arkema France | Method for producing 1-chloro-3,3,3- trifluoropropene |
US11286221B2 (en) | 2018-06-27 | 2022-03-29 | Arkema France | Method for producing 1-chloro-3,3,3-trifluoropropene |
US11952322B2 (en) | 2018-09-26 | 2024-04-09 | Arkema France | Stabilization of 1-chloro-3,3,3-trifluoropropene |
Also Published As
Publication number | Publication date |
---|---|
PL2334750T3 (en) | 2018-07-31 |
FR2937328A1 (en) | 2010-04-23 |
ES2668968T3 (en) | 2018-05-23 |
EP2334750B1 (en) | 2018-04-18 |
HUE037538T2 (en) | 2018-09-28 |
CN102177215A (en) | 2011-09-07 |
FR2937328B1 (en) | 2010-11-12 |
JP2015129633A (en) | 2015-07-16 |
CN106244112A (en) | 2016-12-21 |
CN106244112B (en) | 2023-04-07 |
JP2012505946A (en) | 2012-03-08 |
WO2010043807A1 (en) | 2010-04-22 |
JP6077744B2 (en) | 2017-02-08 |
US10858561B2 (en) | 2020-12-08 |
US20190048241A1 (en) | 2019-02-14 |
PT2334750T (en) | 2018-05-22 |
EP2334750A1 (en) | 2011-06-22 |
JP6151731B2 (en) | 2017-06-21 |
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