US20160122609A1 - Ternary compositions for high-capacity refrigeration - Google Patents
Ternary compositions for high-capacity refrigeration Download PDFInfo
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- US20160122609A1 US20160122609A1 US14/992,387 US201614992387A US2016122609A1 US 20160122609 A1 US20160122609 A1 US 20160122609A1 US 201614992387 A US201614992387 A US 201614992387A US 2016122609 A1 US2016122609 A1 US 2016122609A1
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- tetrafluoropropene
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- 239000000203 mixture Substances 0.000 title claims abstract description 44
- 238000005057 refrigeration Methods 0.000 title claims description 8
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims abstract description 34
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 claims abstract description 19
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000013529 heat transfer fluid Substances 0.000 claims abstract description 8
- 239000002904 solvent Substances 0.000 claims abstract description 5
- 239000000443 aerosol Substances 0.000 claims abstract description 4
- 230000006835 compression Effects 0.000 claims description 9
- 238000007906 compression Methods 0.000 claims description 9
- 239000004604 Blowing Agent Substances 0.000 claims description 4
- 239000000314 lubricant Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000012530 fluid Substances 0.000 description 14
- 239000003507 refrigerant Substances 0.000 description 12
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- 238000004378 air conditioning Methods 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 229910002092 carbon dioxide Inorganic materials 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- VPAYJEUHKVESSD-UHFFFAOYSA-N trifluoroiodomethane Chemical compound FC(F)(F)I VPAYJEUHKVESSD-UHFFFAOYSA-N 0.000 description 3
- 238000010792 warming Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 description 2
- DMUPYMORYHFFCT-UHFFFAOYSA-N 1,2,3,3,3-pentafluoroprop-1-ene Chemical compound FC=C(F)C(F)(F)F DMUPYMORYHFFCT-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- CDOOAUSHHFGWSA-OWOJBTEDSA-N (e)-1,3,3,3-tetrafluoroprop-1-ene Chemical compound F\C=C\C(F)(F)F CDOOAUSHHFGWSA-OWOJBTEDSA-N 0.000 description 1
- NVSXSBBVEDNGPY-UHFFFAOYSA-N 1,1,1,2,2-pentafluorobutane Chemical compound CCC(F)(F)C(F)(F)F NVSXSBBVEDNGPY-UHFFFAOYSA-N 0.000 description 1
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 description 1
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-UHFFFAOYSA-N 0.000 description 1
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 description 1
- HJEORQYOUWYAMR-UHFFFAOYSA-N 2-[(2-butylphenoxy)methyl]oxirane Chemical compound CCCCC1=CC=CC=C1OCC1OC1 HJEORQYOUWYAMR-UHFFFAOYSA-N 0.000 description 1
- HSDVRWZKEDRBAG-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)hexoxymethyl]oxirane Chemical compound C1OC1COC(CCCCC)OCC1CO1 HSDVRWZKEDRBAG-UHFFFAOYSA-N 0.000 description 1
- LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 1
- FNYLWPVRPXGIIP-UHFFFAOYSA-N Triamterene Chemical compound NC1=NC2=NC(N)=NC(N)=C2N=C1C1=CC=CC=C1 FNYLWPVRPXGIIP-UHFFFAOYSA-N 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 150000003851 azoles Chemical class 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 210000005045 desmin Anatomy 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000011551 heat transfer agent Substances 0.000 description 1
- UKACHOXRXFQJFN-UHFFFAOYSA-N heptafluoropropane Chemical compound FC(F)C(F)(F)C(F)(F)F UKACHOXRXFQJFN-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001521 polyalkylene glycol ether Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 239000011555 saturated liquid Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- 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
-
- B01F17/0085—
-
- 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
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/017—Mixtures of 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
- C09K3/00—Materials not provided for elsewhere
- C09K3/30—Materials not provided for elsewhere for aerosols
-
- 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
- C09K2205/10—Components
- C09K2205/12—Hydrocarbons
- C09K2205/126—Unsaturated fluorinated 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
- C09K2205/128—Perfluorinated 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
- C09K2205/22—All components of a mixture being fluoro 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
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/40—Replacement mixtures
Definitions
- the present invention relates to compositions containing 2,3,3,3-tetrafluoropropene and uses thereof as heat-transfer fluids, blowing agents, solvents and aerosols.
- HFCs hydrofluorocarbons
- HFC-134a hydrofluorocarbon (1,1,1,2-tetrafluoroethane: HFC-134a) refrigerant which is less harmful to the ozone layer.
- CFC-12 chlorofluorocarbon
- HFC-134a hydrofluorocarbon (1,1,1,2-tetrafluoroethane: HFC-134a) refrigerant 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 Since carbon dioxide is non-toxic and non-flammable and has a very low GWP, it has been proposed as a refrigerant in air-conditioning systems as a replacement for HFC-134a. However, the use of carbon dioxide has several drawbacks, in particular linked to the very high pressure at which it is used as a refrigerant in the existing apparatuses 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.
- Document WO 2005/105947 teaches the addition to tetrafluoropropene, preferably 1,3,3,3-tetrafluoropropene, of a blowing coagent such as difluoromethane, penta-fluoroethane, tetrafluoroethane, difluoroethane, heptafluoropropane, hexafluoropropane, pentafluoropropane, pentafluorobutane, water and carbon dioxide.
- a blowing coagent such as difluoromethane, penta-fluoroethane, tetrafluoroethane, difluoroethane, heptafluoropropane, hexafluoropropane, pentafluoropropane, pentafluorobutane, water and carbon dioxide.
- Quaternary mixtures comprising 1,1,1,2,3-pentafluoropropene (HFO-1225ye) in combination with difluoromethane, 2,3,3,3-tetrafluoropropene and HFC-134a were disclosed in this document. However, 1,1,1,2,3-pentafluoropropene is toxic.
- CF 3 I Quaternary mixtures comprising 2,3,3,3-tetrafluoropropene in combination with iodotrifluoromethane (CF 3 I), HFC-32 and HFC-134a have also been disclosed in document WO 2006/094303.
- CF 3 I has a non-zero ODP and poses stability and corrosion problems.
- compositions used as a heat-transfer fluid in the present invention have a critical temperature greater than 87° C. (critical temperature of R410A is 70.5° C.). These compositions can be used in heat pumps for providing heat at temperatures up to 65° C. but also at higher temperatures up to 87° C. (temperature range at which R410A cannot be used).
- compositions used as heat-transfer fluid in the present invention have temperatures at the compressor outlet equivalent to the values given by R-410A.
- the condenser pressures are lower than the pressures of R-410A and the compression ratios are also lower. These compositions can replace R-410A without changing compressor technology.
- compositions used as a heat-transfer fluid in the present invention have saturation vapor densities which are less than the saturated vapor density of R410A.
- the volumetric capacities given by these compositions are equivalent to the volumetric capacity of R410A (between 90 and 99%). By virtue of these properties, these compositions can operate with smaller pipe diameters and therefore less pressure drop in the steam pipework, thereby increasing the performance levels of the equipment.
- compositions according to the present invention are characterized in that they essentially contain from 15 to 50% by weight of 2,3,3,3-tetrafluoropropene, from 5 to 40% by weight of HFC-134a and from 45 to 60% by weight, preferably from 45 to 50% by weight of HFC-32.
- compositions according to the present invention can be used as heat-transfer fluids, preferably in compression systems and advantageously with exchangers operating in counterflow mode or in cross-flow mode with counterflow tendency. They are particularly suitable for systems of high-capacity refrigeration per unit volume swept by the compressor.
- heat-transfer fluids In compression systems, the heat exchange between the refrigerant and the heat sources takes place by means of heat-transfer fluids. These heat-transfer fluids are in the gaseous state (the air in air-conditioning and direct expansion refrigeration), liquid state (the water in domestic heat pumps, glycolated water) or two-phase state.
- compositions according to the present invention are advantageously used in stationary air conditioning, preferably as a replacement for R-410A.
- compositions according to the present invention can be stabilized.
- the stabilizer preferably represents at most 5% by weight relative to the total composition.
- nitromethane ascorbic acid, terephthalic acid, azoles such as tolutriazole or benzotriazole, phenolic compounds such as tocopherol, hydroquinone, t-butyl hydroquinone or 2,6-di-tert-butyl-4-methylphenol, epoxides (alkyl, optionally fluorinated or perfluorinated, or alkenyl or aromatic) 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
- compositions according to the present invention as a heat-transfer agent, can be employed in the presence of lubricants such as mineral oil, alkylbenzene, polyalkylene glycol and polyvinyl ether.
- compositions according to the present invention can also be used as blowing agents, aerosols and solvents.
- the RK-Soave equation is used for calculating the densities, enthalpies, entropies and liquid/vapor equilibrium data of the mixtures.
- the use of this equation requires knowledge of the properties of the pure bodies used in the mixtures in question and also the interaction coefficients for each binary mixture.
- HFC-32, HFC-134a
- the data of the temperature-pressure curve for HFO-1234yf are measured by the static method.
- the critical temperature and the critical pressure are measured using a C80 calorimeter sold by Setaram.
- the densities, at saturation as a function of temperature, are measured using the vibrating tube densitometer technology developed by the laboratories of the autoimmune des Mines of Paris.
- the RK-Soave equation uses binary interaction coefficients to represent the behavior of the products in mixtures.
- the coefficients are calculated as a function of the experimental liquid/vapor equilibrium data.
- the technique used for the liquid/vapor equilibrium measurements is the static-cell analytical method.
- the equilibrium cell comprises a sapphire tube and is equipped with two electromagnetic ROLSITM samplers. It is immersed in a cryothermostat bath (HUBER HS40). A magnetic stirrer with a field drive rotating at varying speed is used to accelerate reaching the equilibria.
- the analysis of the samples is carried out by gas chromatography (HP5890 series II) using a katharometer (TCD).
- the liquid/vapor equilibrium data for the binary mixture HFC-134a/HFC-32 are available from Refprop. Two isotherms ( ⁇ 20° C. and 20° C.) and one isobar (30 bar) are used to calculate the interaction coefficients for this binary mixture.
- a compression system equipped with a counterflow condenser and evaporator, with a screw compressor and with an expansion valve is considered.
- the system operates with 15° C. of overheat and 5° C. of undercooling.
- the minimum temperature difference between the secondary fluid and the refrigerant is considered to be about 5° C.
- the isentropic efficiency of the compressors depends on the compression ratio. This efficiency is calculated according to the following equation:
- ⁇ isen a - b ⁇ ( ⁇ - c ) 2 - d ⁇ - e ( 1 )
- the % CAP is the percentage of the ratio of the volumetric capacity supplied by each product over the capacity of R410A.
- the coefficient of performance is defined as being the useful power supplied by the system over the power provided or consumed by the system.
- the Lorenz coefficient of performance (COPLorenz) is a reference coefficient of performance. It is a function of temperatures and is used for comparing the COPs of various fluids.
- the Lorenz coefficient of performance is defined as follows:
- T average condenser T inlet condenser ⁇ T outlet condenser (2)
- T average evaporator T outlet evaporator ⁇ T inlet evaporator (3)
- the Lorenz COP in the case of air-conditioning and refrigeration is:
- the Lorenz COP in the case of heating is:
- the coefficient of performance of the Lorenz cycle is calculated as a function of the corresponding temperatures.
- the % COP/COPLorenz is the ratio of the COP of the system relative to the COP of the corresponding Lorenz cycle.
- the compression system In heating mode, the compression system operates between a temperature for inlet of the refrigerant into the evaporator of ⁇ 5° C. and a temperature for inlet of the refrigerant into the condenser of 50° C.
- the system supplies heat at 45° C.
- compositions according to the invention under the heating mode operating conditions are given in table 1.
- values of the constituents (HFO-1234yf, HFC-32, HFC-134a) for each composition are given as percentage by weight.
- the compression system In cooling mode, the compression system operates between a temperature for inlet of the refrigerant into the evaporator of ⁇ 5° C. and a temperature for inlet of the refrigerant into the condenser of 50° C.
- the system supplies refrigeration at 0° C.
- compositions according to the invention under the cooling mode operating conditions are given in table 2.
- values of the constituents (HFO-1234yf, HFC-32, HFC-134a) for each composition are given as percentage by weight.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Dispersion Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Lubricants (AREA)
Abstract
Compositions containing 2,3,3,3-tetrafluoropropene and to the uses thereof as heat transfer fluid, expansion agents, solvents and aerosol. Compositions of between 15 and 50 wt. % of 2,3,3,3-tetrafluoropropene, between 5 and 40 wt. % of HFC-134a and between 45 and 60 wt. %, preferably between 45 and 50 wt. %, of HFC-32.
Description
- The present application is a continuation of U.S. application Ser. No. 13/390,379, filed on Feb. 14, 2012, which is a U.S. national stage application of International Application No. PCT/FR2010/051745, filed on Aug. 20, 2010, which claims the benefit of French Application No. 0956248, filed on Sep. 11, 2009. The entire contents of each of U.S. application Ser. No. 13/390,379, International Application No. PCT/FR2010/051745, and French Application No. 0956248 are hereby incorporated herein by reference in their entirety.
- The present invention relates to compositions containing 2,3,3,3-tetrafluoropropene and uses thereof as heat-transfer fluids, blowing agents, solvents and aerosols.
- The problems posed by substances which delete the atmospheric ozone layer (ODP: ozone depletion potential) were addressed in 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, including hydrochlorofluorocarbons (HCFCs).
- The refrigeration and air-conditioning industry has invested a great deal in the replacement of these refrigerants, and as a result, hydrofluorocarbons (HFCs) have been marketed.
- The (hydro)chlorofluorocarbons used as blowing agents or solvents have also been replaced with HFCs.
- In the automotive industry, the air-conditioning systems for vehicles sold in many countries have changed from a chlorofluorocarbon (CFC-12) refrigerant to a hydrofluorocarbon (1,1,1,2-tetrafluoroethane: HFC-134a) refrigerant 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 considered to have 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.
- Since carbon dioxide is non-toxic and non-flammable and has a very low GWP, it has been proposed as a refrigerant in air-conditioning systems as a replacement for HFC-134a. However, the use of carbon dioxide has several drawbacks, in particular linked to the very high pressure at which it is used as a refrigerant in the existing apparatuses and technologies.
- 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.
- Document WO 2005/105947 teaches the addition to tetrafluoropropene, preferably 1,3,3,3-tetrafluoropropene, of a blowing coagent such as difluoromethane, penta-fluoroethane, tetrafluoroethane, difluoroethane, heptafluoropropane, hexafluoropropane, pentafluoropropane, pentafluorobutane, water and carbon dioxide.
- Document WO 2006/094303 discloses binary compositions of 2,3,3,3-tetrafluoropropene (HFO-1234yf) with difluoromethane (HFC-32), and of 2,3,3,3-tetrafluoropropene with 1,1,1,2-tetrafluoroethane (HFC-134a).
- Quaternary mixtures comprising 1,1,1,2,3-pentafluoropropene (HFO-1225ye) in combination with difluoromethane, 2,3,3,3-tetrafluoropropene and HFC-134a were disclosed in this document. However, 1,1,1,2,3-pentafluoropropene is toxic.
- Quaternary mixtures comprising 2,3,3,3-tetrafluoropropene in combination with iodotrifluoromethane (CF3I), HFC-32 and HFC-134a have also been disclosed in document WO 2006/094303. However, CF3I has a non-zero ODP and poses stability and corrosion problems.
- The applicant has now developed 2,3,3,3-tetrafluoropropene compositions which do not have the abovementioned drawbacks and have both a zero ODP and a GWP which is lower than that of the existing heat-transfer fluids such as R410A (binary mixture of pentafluoroethane (50% by weight) and HFC-32 (50% by weight)).
- The compositions used as a heat-transfer fluid in the present invention have a critical temperature greater than 87° C. (critical temperature of R410A is 70.5° C.). These compositions can be used in heat pumps for providing heat at temperatures up to 65° C. but also at higher temperatures up to 87° C. (temperature range at which R410A cannot be used).
- The compositions used as heat-transfer fluid in the present invention have temperatures at the compressor outlet equivalent to the values given by R-410A. The condenser pressures are lower than the pressures of R-410A and the compression ratios are also lower. These compositions can replace R-410A without changing compressor technology.
- The compositions used as a heat-transfer fluid in the present invention have saturation vapor densities which are less than the saturated vapor density of R410A. The volumetric capacities given by these compositions are equivalent to the volumetric capacity of R410A (between 90 and 99%). By virtue of these properties, these compositions can operate with smaller pipe diameters and therefore less pressure drop in the steam pipework, thereby increasing the performance levels of the equipment.
- The compositions according to the present invention are characterized in that they essentially contain from 15 to 50% by weight of 2,3,3,3-tetrafluoropropene, from 5 to 40% by weight of HFC-134a and from 45 to 60% by weight, preferably from 45 to 50% by weight of HFC-32.
- The compositions according to the present invention can be used as heat-transfer fluids, preferably in compression systems and advantageously with exchangers operating in counterflow mode or in cross-flow mode with counterflow tendency. They are particularly suitable for systems of high-capacity refrigeration per unit volume swept by the compressor.
- In compression systems, the heat exchange between the refrigerant and the heat sources takes place by means of heat-transfer fluids. These heat-transfer fluids are in the gaseous state (the air in air-conditioning and direct expansion refrigeration), liquid state (the water in domestic heat pumps, glycolated water) or two-phase state.
- There are various modes of transfer:
-
- the two fluids are arranged in parallel and travel in the same direction: co-flow (antimethodic) mode;
- the two fluids are arranged in parallel but travel in the opposite direction: counterflow (methodic) mode;
- the two fluids are positioned perpendicularly: cross-flow mode. The cross-flow may be with co-flow or counterflow tendency;
- one of the two fluids makes a U-turn in a wider pipe, which the second fluid passes through. This configuration is comparable to a co-flow exchanger over half the length, and for the other half, to a counterflow exchanger: pinhead mode.
- The compositions according to the present invention are advantageously used in stationary air conditioning, preferably as a replacement for R-410A.
- The compositions according to the present invention can be stabilized. The stabilizer preferably represents at most 5% by weight relative to the total composition.
- As stabilizers, mention may in particular be made of nitromethane, ascorbic acid, terephthalic acid, azoles such as tolutriazole or benzotriazole, phenolic compounds such as tocopherol, hydroquinone, t-butyl hydroquinone or 2,6-di-tert-butyl-4-methylphenol, epoxides (alkyl, optionally fluorinated or perfluorinated, or alkenyl or aromatic) such as n-butyl glycidyl ether, hexanediol diglycidyl ether, allyl glycidyl ether or butylphenyl glycidyl ether, phosphites, phosphates, phosphonates, thiols and lactones.
- The compositions according to the present invention, as a heat-transfer agent, can be employed in the presence of lubricants such as mineral oil, alkylbenzene, polyalkylene glycol and polyvinyl ether.
- The compositions according to the present invention can also be used as blowing agents, aerosols and solvents.
- The RK-Soave equation is used for calculating the densities, enthalpies, entropies and liquid/vapor equilibrium data of the mixtures. The use of this equation requires knowledge of the properties of the pure bodies used in the mixtures in question and also the interaction coefficients for each binary mixture.
- The data required for each pure body are:
- The boiling point, the critical temperature and the critical pressure, the curve of pressure as a function of temperature starting from the boiling point up to the critical point, and the saturated liquid and saturated vapor densities as a function of temperature.
- The data on these products aer published in the ASHRAE Handbook 2005 chapter 20, and are also available from Refrop (software developed by NIST for calculating the properties of refrigerants).
- The data of the temperature-pressure curve for HFO-1234yf are measured by the static method. The critical temperature and the critical pressure are measured using a C80 calorimeter sold by Setaram. The densities, at saturation as a function of temperature, are measured using the vibrating tube densitometer technology developed by the laboratories of the Ecole des Mines of Paris.
- The RK-Soave equation uses binary interaction coefficients to represent the behavior of the products in mixtures. The coefficients are calculated as a function of the experimental liquid/vapor equilibrium data.
- The technique used for the liquid/vapor equilibrium measurements is the static-cell analytical method. The equilibrium cell comprises a sapphire tube and is equipped with two electromagnetic ROLSITM samplers. It is immersed in a cryothermostat bath (HUBER HS40). A magnetic stirrer with a field drive rotating at varying speed is used to accelerate reaching the equilibria. The analysis of the samples is carried out by gas chromatography (HP5890 series II) using a katharometer (TCD).
- The liquid/vapor equilibrium measurements on the binary mixture HFC-32/HFO-1234yf are carried out for the following isotherms: −10° C., 30° C. and 70° C.
- The liquid/vapor equilibrium measurements on the binary mixture HFC-134a/HFO-1234yf are carried out for the following isotherms: 20° C.
- The liquid/vapor equilibrium data for the binary mixture HFC-134a/HFC-32 are available from Refprop. Two isotherms (−20° C. and 20° C.) and one isobar (30 bar) are used to calculate the interaction coefficients for this binary mixture.
- A compression system equipped with a counterflow condenser and evaporator, with a screw compressor and with an expansion valve is considered.
- The system operates with 15° C. of overheat and 5° C. of undercooling. The minimum temperature difference between the secondary fluid and the refrigerant is considered to be about 5° C.
- The isentropic efficiency of the compressors depends on the compression ratio. This efficiency is calculated according to the following equation:
-
- For a screw compressor, the constants a, b, c, d and e of the isentropic efficiency equation (1) are calculated according to the standard data published in the “Handbook of air conditioning and refrigeration, page 11.52”.
- The % CAP is the percentage of the ratio of the volumetric capacity supplied by each product over the capacity of R410A.
- The coefficient of performance (COP) is defined as being the useful power supplied by the system over the power provided or consumed by the system.
- The Lorenz coefficient of performance (COPLorenz) is a reference coefficient of performance. It is a function of temperatures and is used for comparing the COPs of various fluids.
- The Lorenz coefficient of performance is defined as follows:
- (The temperatures T are in K)
-
T average condenser =T inlet condenser −T outlet condenser (2) -
T average evaporator =T outlet evaporator −T inlet evaporator (3) - The Lorenz COP in the case of air-conditioning and refrigeration is:
-
- The Lorenz COP in the case of heating is:
-
- For each composition, the coefficient of performance of the Lorenz cycle is calculated as a function of the corresponding temperatures.
- The % COP/COPLorenz is the ratio of the COP of the system relative to the COP of the corresponding Lorenz cycle.
- In heating mode, the compression system operates between a temperature for inlet of the refrigerant into the evaporator of −5° C. and a temperature for inlet of the refrigerant into the condenser of 50° C. The system supplies heat at 45° C.
- The performance levels of the compositions according to the invention under the heating mode operating conditions are given in table 1. The values of the constituents (HFO-1234yf, HFC-32, HFC-134a) for each composition are given as percentage by weight.
-
TABLE 1 Evap Comp outlet outlet Cond Evap Cond Ratio Comp % % COP/ temp (° C.) temp (° C.) outlet T (° C.) P (bar) P (bar) (w/w) Glide efficiency CAP COPLorenz R410A −5 101 50 6.8 30.6 4.5 0.07 79.6 100 58.8 HFO- HFC- HFC- 1234yf 32 134a 45 50 5 −2 97 46 5.8 24.8 4.2 3.18 80.3 92 62.9 40 55 5 −2 101 47 6.0 25.8 4.3 2.63 80.1 95 62.6 25 50 25 −1 99 46 5.6 23.7 4.3 3.74 80.2 91 64.1 20 55 25 −2 102 46 5.7 24.5 4.3 3.47 80.1 93 63.8 15 60 25 −2 106 47 5.8 25.2 4.3 3.23 80.0 95 63.5 - In cooling mode, the compression system operates between a temperature for inlet of the refrigerant into the evaporator of −5° C. and a temperature for inlet of the refrigerant into the condenser of 50° C. The system supplies refrigeration at 0° C.
- The performance levels of the compositions according to the invention under the cooling mode operating conditions are given in table 2. The values of the constituents (HFO-1234yf, HFC-32, HFC-134a) for each composition are given as percentage by weight.
-
TABLE 2 Evap Comp outlet outlet Cond Evap Cond Ratio Comp % % COP/ temp (° C.) temp (° C.) outlet T (° C.) P (bar) P (bar) (w/w) Glide efficiency CAP COPLorenz R410A −5 101 50 6.8 30.6 4.5 0.07 79.6 100 50.4 HFO- HFC- HFC- 1234yf 32 134a 50 45 5 −1 94 45 5.7 23.7 4.2 3.76 80.5 92 55.5 45 50 5 −2 97 46 5.8 24.8 4.2 3.18 80.3 95 55.1 40 55 5 −2 101 47 6.0 25.8 4.3 2.63 80.1 98 54.8 30 45 25 −1 96 46 5.4 22.9 4.2 4.04 80.3 92 56.7 25 50 25 −1 99 46 5.6 23.7 4.3 3.74 80.2 94 56.4 20 55 25 −2 102 46 5.7 24.5 4.3 3.47 80.1 97 56.2 15 60 25 −2 106 47 5.8 25.2 4.3 3.23 80.0 99 55.9 15 45 40 −1 98 45 5.2 22.1 4.3 4.48 80.2 90 57.3
Claims (9)
1. A composition essentially containing from 15 to 50% by weight of 2,3,3,3-tetrafluoropropene, from 5 to 40% by weight of HFC-134a and from 45 to 60% by weight of HFC-32, preferably from 45 to 50% by weight of HFC-32.
2. The composition as claimed in claim 1 , characterized in that it is stabilized.
3. A heat-transfer fluid comprising the composition as claimed in claim 1 .
4. The heat-transfer fluid as claimed in claim 3 , characterized in that it is used in compression refrigeration systems, preferably with exchangers operating in counterflow mode.
5. The heat-transfer fluid as claimed in claim 3 , characterized in that it is used as a replacement for R-410A.
6. The heat-transfer fluid as claimed in claim 3 , characterized in that it is employed in the presence of a lubricant.
7. Blowing agents comprising the compositions as claimed in claim 1 .
8. Solvents comprising the compositions as claimed in claim 1 .
9. Aerosols comprising the compositions as claimed in claim 1 .
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| US14/992,387 US20160122609A1 (en) | 2009-09-11 | 2016-01-11 | Ternary compositions for high-capacity refrigeration |
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| FR0956248A FR2950070B1 (en) | 2009-09-11 | 2009-09-11 | TERNARY COMPOSITIONS FOR HIGH CAPACITY REFRIGERATION |
| FR0956248 | 2009-09-11 | ||
| PCT/FR2010/051745 WO2011030031A1 (en) | 2009-09-11 | 2010-08-20 | Ternary compositions for high-capacity refrigeration |
| US201213390379A | 2012-02-14 | 2012-02-14 | |
| US14/992,387 US20160122609A1 (en) | 2009-09-11 | 2016-01-11 | Ternary compositions for high-capacity refrigeration |
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| US13/390,379 Continuation US9267064B2 (en) | 2009-09-11 | 2010-08-20 | Ternary compositions for high-capacity refrigeration |
| PCT/FR2010/051745 Continuation WO2011030031A1 (en) | 2009-09-11 | 2010-08-20 | Ternary compositions for high-capacity refrigeration |
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-
2009
- 2009-09-11 FR FR0956248A patent/FR2950070B1/en not_active Expired - Fee Related
-
2010
- 2010-08-20 RU RU2012114138/05A patent/RU2544662C2/en not_active IP Right Cessation
- 2010-08-20 CN CN201080040355.3A patent/CN102482557B/en not_active Expired - Fee Related
- 2010-08-20 WO PCT/FR2010/051745 patent/WO2011030031A1/en not_active Ceased
- 2010-08-20 EP EP10762997.4A patent/EP2475732B1/en not_active Not-in-force
- 2010-08-20 JP JP2012528412A patent/JP5866284B2/en not_active Expired - Fee Related
- 2010-08-20 PT PT107629974T patent/PT2475732T/en unknown
- 2010-08-20 CN CN201510454269.1A patent/CN104974719B/en not_active Expired - Fee Related
- 2010-08-20 US US13/390,379 patent/US9267064B2/en not_active Expired - Fee Related
- 2010-08-20 BR BR112012005095A patent/BR112012005095A2/en not_active Application Discontinuation
-
2015
- 2015-09-09 JP JP2015177323A patent/JP6138205B2/en not_active Expired - Fee Related
-
2016
- 2016-01-11 US US14/992,387 patent/US20160122609A1/en not_active Abandoned
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Also Published As
| Publication number | Publication date |
|---|---|
| FR2950070B1 (en) | 2011-10-28 |
| JP2016053162A (en) | 2016-04-14 |
| CN102482557B (en) | 2015-09-02 |
| CN102482557A (en) | 2012-05-30 |
| EP2475732B1 (en) | 2018-05-16 |
| JP6138205B2 (en) | 2017-05-31 |
| FR2950070A1 (en) | 2011-03-18 |
| EP2475732A1 (en) | 2012-07-18 |
| CN104974719A (en) | 2015-10-14 |
| US9267064B2 (en) | 2016-02-23 |
| US20120153213A1 (en) | 2012-06-21 |
| RU2544662C2 (en) | 2015-03-20 |
| WO2011030031A1 (en) | 2011-03-17 |
| RU2012114138A (en) | 2013-10-20 |
| JP2013504643A (en) | 2013-02-07 |
| BR112012005095A2 (en) | 2016-05-03 |
| JP5866284B2 (en) | 2016-02-17 |
| PT2475732T (en) | 2018-06-26 |
| CN104974719B (en) | 2020-05-19 |
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Legal Events
| Date | Code | Title | Description |
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| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- AFTER EXAMINER'S ANSWER OR BOARD OF APPEALS DECISION |