WO2007148046A1 - Heat transfer compositions - Google Patents
Heat transfer compositions Download PDFInfo
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- WO2007148046A1 WO2007148046A1 PCT/GB2007/002174 GB2007002174W WO2007148046A1 WO 2007148046 A1 WO2007148046 A1 WO 2007148046A1 GB 2007002174 W GB2007002174 W GB 2007002174W WO 2007148046 A1 WO2007148046 A1 WO 2007148046A1
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- 239000000203 mixture Substances 0.000 title claims abstract description 137
- 238000012546 transfer Methods 0.000 title claims abstract description 25
- VPAYJEUHKVESSD-UHFFFAOYSA-N trifluoroiodomethane Chemical compound FC(F)(F)I VPAYJEUHKVESSD-UHFFFAOYSA-N 0.000 claims abstract description 26
- 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 claims abstract description 24
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 claims abstract description 21
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims abstract description 21
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims abstract description 12
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 claims abstract description 6
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 18
- 239000003507 refrigerant Substances 0.000 claims description 18
- 238000004378 air conditioning Methods 0.000 claims description 15
- 239000002904 solvent Substances 0.000 claims description 14
- 238000005057 refrigeration Methods 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 10
- -1 R- 125 Chemical compound 0.000 claims description 9
- 239000006260 foam Substances 0.000 claims description 8
- 238000001704 evaporation Methods 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 7
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 5
- 239000003063 flame retardant Substances 0.000 claims description 5
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 5
- 239000002028 Biomass Substances 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- 239000000314 lubricant Substances 0.000 claims description 4
- 239000011159 matrix material Substances 0.000 claims description 4
- 238000010248 power generation Methods 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 239000003381 stabilizer Substances 0.000 claims description 4
- AWTOFSDLNREIFS-UHFFFAOYSA-N 1,1,2,2,3-pentafluoropropane Chemical compound FCC(F)(F)C(F)F AWTOFSDLNREIFS-UHFFFAOYSA-N 0.000 claims description 3
- 239000013529 heat transfer fluid Substances 0.000 claims description 3
- 238000012986 modification Methods 0.000 claims description 3
- 230000004048 modification Effects 0.000 claims description 3
- 229920001289 polyvinyl ether Polymers 0.000 claims description 3
- QTHRIIFWIHUMFH-UHFFFAOYSA-N 3-chloropropyl dihydrogen phosphate Chemical compound OP(O)(=O)OCCCCl QTHRIIFWIHUMFH-UHFFFAOYSA-N 0.000 claims description 2
- 239000004604 Blowing Agent Substances 0.000 claims description 2
- 239000005696 Diammonium phosphate Substances 0.000 claims description 2
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical class O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 239000004793 Polystyrene Substances 0.000 claims description 2
- PQYJRMFWJJONBO-UHFFFAOYSA-N Tris(2,3-dibromopropyl) phosphate Chemical compound BrCC(Br)COP(=O)(OCC(Br)CBr)OCC(Br)CBr PQYJRMFWJJONBO-UHFFFAOYSA-N 0.000 claims description 2
- 229910000410 antimony oxide Inorganic materials 0.000 claims description 2
- 150000001491 aromatic compounds Chemical class 0.000 claims description 2
- 150000001555 benzenes Chemical class 0.000 claims description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical class BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 claims description 2
- 238000004140 cleaning Methods 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims description 2
- 229910000388 diammonium phosphate Inorganic materials 0.000 claims description 2
- 235000019838 diammonium phosphate Nutrition 0.000 claims description 2
- 150000002118 epoxides Chemical class 0.000 claims description 2
- 239000003822 epoxy resin Substances 0.000 claims description 2
- 150000002334 glycols Chemical class 0.000 claims description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical class IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 claims description 2
- 239000002480 mineral oil Substances 0.000 claims description 2
- 235000010446 mineral oil Nutrition 0.000 claims description 2
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical class [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 235000021317 phosphate Nutrition 0.000 claims description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 2
- 229920000647 polyepoxide Polymers 0.000 claims description 2
- 229920005862 polyol Polymers 0.000 claims description 2
- 229920005990 polystyrene resin Polymers 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- 239000004800 polyvinyl chloride Chemical class 0.000 claims description 2
- 229920000915 polyvinyl chloride Chemical class 0.000 claims description 2
- 239000003380 propellant Substances 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- 238000009420 retrofitting Methods 0.000 claims description 2
- 229920002545 silicone oil Polymers 0.000 claims description 2
- 229920001169 thermoplastic Polymers 0.000 claims description 2
- 229920005992 thermoplastic resin Polymers 0.000 claims description 2
- HQUQLFOMPYWACS-UHFFFAOYSA-N tris(2-chloroethyl) phosphate Chemical compound ClCCOP(=O)(OCCCl)OCCCl HQUQLFOMPYWACS-UHFFFAOYSA-N 0.000 claims description 2
- SUIOPXSLPPMBJN-UHFFFAOYSA-N 1,3-dichloropropyl dihydrogen phosphate Chemical compound OP(O)(=O)OC(Cl)CCCl SUIOPXSLPPMBJN-UHFFFAOYSA-N 0.000 claims 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims 1
- 125000002897 diene group Chemical group 0.000 claims 1
- CQXADFVORZEARL-UHFFFAOYSA-N Rilmenidine Chemical compound C1CC1C(C1CC1)NC1=NCCO1 CQXADFVORZEARL-UHFFFAOYSA-N 0.000 abstract description 2
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 abstract description 2
- 239000012530 fluid Substances 0.000 description 21
- 239000007788 liquid Substances 0.000 description 11
- 239000007789 gas Substances 0.000 description 6
- 238000010792 warming Methods 0.000 description 5
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 4
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000009834 vaporization Methods 0.000 description 3
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 239000011555 saturated liquid Substances 0.000 description 2
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical class F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- DHNUXDYAOVSGII-UHFFFAOYSA-N tris(1,3-dichloropropyl) phosphate Chemical compound ClCCC(Cl)OP(=O)(OC(Cl)CCCl)OC(Cl)CCCl DHNUXDYAOVSGII-UHFFFAOYSA-N 0.000 description 1
Classifications
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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
- 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
- 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
-
- 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
- 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
-
- 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
- the invention relates to heat transfer compositions, and in particular to heat transfer compositions comprising at least one flammable component.
- the properties preferred in a refrigerant include low toxicity, non-flammability, non-corrosivity, high stability and freedom from objectionable odour.
- Other desirable properties are ready compressibility at pressures below 25 bars, low discharge temperature on compression, high refrigeration capacity, high efficiency (high coefficient of performance) and an evaporator pressure in excess of 1 bar at the desired evaporation temperature.
- Dichlorodifluoromethane (refrigerant R- 12) possesses a suitable combination of properties and was for many years the most widely used refrigerant. Due to international concern that fully and partially halogenated chlorofluorocarbons, such as dichlorodifluoromethane and chlorodifluoromethane, were damaging the earth's protective ozone layer, there was general agreement that their manufacture and use should be severely restricted and eventually phased out completely. The use of dichlorofiuoromethane was phased out in the 1990's.
- R- 134a 1,1,1,2-tetrafluoroethane
- R-12 1,1,1,2-tetrafluoroethane
- GWP global warming potential
- a heat transfer composition comprising (i) at least one flammable component selected from R-1234yf and R- 152a,
- composition has a GWP of less than that of the at least one nonflammable (hydro)fluorocarbon.
- PreferabTy7tEe composltion ' comprises substantially no R--12-34yf ⁇
- the composition comprises substantially no R-152a.
- the at least one non-flammable, (hydro)fluorocarbon is selected from R-134a, R-134, R-125, R-245fa, R-245ca, R-245cb, R-236fa and R-227ea.
- the at least one (hydro)fluorocarbon is selected from R- 134a and R-245fa.
- the composition comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about 30% by weight of the composition.
- the composition comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about 10% by weight of the composition.
- the composition comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about 6% by weight of the composition.
- the composition comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about 5% by weight of the composition.
- the composition is azeotrope-like.
- the composition has a GWP of about 750 or less.
- the composition has a GWP of about 500 or less.
- the composition has a GWP of about 250 or less.
- the composition has a GWP of about 150 or less.
- the composition has a GWP of about 100 or less.
- the composition further comprises a lubricant.
- the lubricant is selected from the group consisting of mineral oil, silicone oil, polyalkyl benzenes (PABs) 5 polyol esters (POEs), polyalkylene glycols (PAGs), polyalkylene glycol esters (PAG esters), polyvinyl ethers (PVEs), poly (alpha-olefms) and combinations thereof.
- PABs polyalkyl benzenes
- PESs polyol esters
- PAGs polyalkylene glycols
- PAG esters polyalkylene glycol esters
- PVEs polyvinyl ethers
- poly (alpha-olefms) poly (alpha-olefms) and combinations thereof.
- composition further comprises a stabiliser.
- the stabiliser is selected from the group consisting of diene- based compounds, phosphates, phenol compounds and epoxides, and mixtures thereof.
- the composition further comprises an additional flame retardant.
- the additional flame retardant is selected from the group consisting of tri-(2-chloroethyl)-phosphate, (chloropropyl)phosphate, tri-
- the composition is a refrigerant composition.
- a heat transfer device containing a composition of the invention.
- the heat transfer device is a refrigeration device.
- the heat transfer device is selected from group consisting of automotive air conditioning systems, residential air conditioning S3fstems, commercial air conditioning systems, residential refrigerator systems, residential freezer systems, commercial refrigerator systems, commercial freezer systems, chiller air conditioning systems, chiller refrigeration systems, heat pump systems.
- the heat transfer device contains a centrifugal-type compressor.
- a blowing agent comprising a composition of the invention.
- a foamable composition comprising one or more components capable of forming foam and a composition of the invention.
- the one or more components capable of forming foam are selected from polyurethanes, thermoplastic polymers and resins, such as polystyrene, and epoxy resins.
- a foam obtainable from the foamable composition of the invention.
- the foam comprises a composition of the invention.
- a sprayable composition comprising a material to be sprayed and a propellant comprising a composition of the invention.
- a method for cooling an article which comprises condensing a composition of the invention and thereafter evaporating said composition in the vicinity of the article to be cooled.
- a method for heating an article which comprises condensing a composition of the invention in the vicinity of the article to be heated and thereafter evaporating said composition.
- a method for extracting a substance from biomass comprising contacting the biomass with a solvent comprising a composition of the invention, and separating the substance from the solvent.
- a method of cleaning an article comprising contacting the article with a solvent comprising a composition of the invention.
- a method for extracting a material from an aqueous solution comprising contacting the aqueous solution with a solvent comprising a composition of the invention, and separating the substance from the solvent.
- a method for extracting a material from a particulate solid matrix comprising contacting the particulate solid matrix with a solvent comprising a composition of the invention, and separating the substance from the solvent.
- a mechanical power generation device containing a composition of the invention.
- the mechanical power generation device is adapted to use a Rankine Cycle or modification thereof to generate work from heat.
- a method of retrofitting a refrigeration device comprising the step of removing an existing heat transfer fluid, and introducing a composition of the invention.
- CF 3 I trifhioroiodomethane
- CF 3 I has been proposed for use as a flame retardant in heat transfer compositions.
- CF 3 I has a number of disadvantages. Firstly, CF 3 I is relatively expensive, partly due to the relative scarcity of the element iodine. Also, CF 3 I has a high molecular weight of 195.91. In practice, this means that a relatively large and expensive amount of CF 3 I must be combined with a flammable heat transfer fluid in order to result in significantly reduced flammability. Also, the use of such relatively high amounts of CF 3 I can lead to increased weight of fluid to be used in a heat transfer device, such as an automotive air- conditioning system, as compared to a traditional heat transfer composition.
- blending a non-flammable (hydro)fluorocarbon fluid with a flammable (hydro)fluorocarbon fluid and CF 3 I can result in a composition having an acceptable GWP and an acceptable flammability.
- the use of at least one nonflammable (hydro)fluorocarbon fluid with a relatively high GWP can result in a heat transfer composition of reduced flammability and acceptable GWP.
- the level of CF 3 I needed to give the required level of non- flammability can be reduced.
- compositions In some circumstances, it is preferred for the compositions to have a GWP of about 150 or less. However, for other applications, it may be acceptable for composition to have a higher GWP, for example a GWP of up to 250, 500 or 750.
- Preferred flammable refrigerants are 2,3,3,3-tetrafluoropropene (R-1234yf) and 1,1-difmoroethane (R-152a).
- Preferred non-flammable (hydro)fluorocarbon fluids are R- 134a, R- 134, R- 125, R-245fa, R-245ca, R-245cb, R-236fa andR-227ea.
- the non-flammable (hydro)fluorocarbon components may be present in the composition preferably in a range from about 1 to about 30% by weight.
- the maximum proportion preferred for any given application will be determined by the fluid's Greenhouse Warming Potential (GWP) and the desired GWP of the formulated blend of flammable fluid, CF 3 I and non- flammable fluid.
- GWP Greenhouse Warming Potential
- the flammability of R-1234yf when mixed with air and CF 3 I has been determined according to the methodology of Addendum p to ASHRAE Standard 34, using the ASTM E681 protocol in a 12 litre flask with electronic ignition.
- the test temperature used was 60 0 C and the humidity was equivalent to 50% relative humidity at 23 0 C.
- the flammability limits of R-1234yf in air were found to be 5.5% to 13.4% v/v.
- the minimum quantity of CF 3 I required to render the fuel nonflammable in air at all concentrations was found to be 19% v/v when mixed with R-1234yf.
- the test was repeated, using as fuel a mixture of R-1234yf with R-134a in the molar ratio 86:14.
- the flammability limits of this fuel mixture in air were found to be 6.5% to 15% v/v.
- the minimum quantity of CF 3 I required to render the fuel non-flammable in air at all concentrations was found to be 18% v/v.
- thermodynamic properties of a fluid for estimation of its performance as a refrigerant or air conditioning system working fluid are:
- the heat capacity of the gas and liquid states Two mixtures have been studied.
- the first mixture is a binary mixture of R- 1234yf with CF 3 I, such that the quantity Of CF 3 I in the mixture is sufficient to render the mixture non-flammable in air at all concentrations according to the flammability test data determined above.
- the above binary mixture was compared with a ternary mixture of the invention, comprising R-1234yf/R-134a/CF 3 I, selected such that the molar ratio of R-1234yf:R-134a is 86:14 and the mixture is non-flammable in air at all concentrations. This ⁇ elds a mixture composition of R-1234yf/R- 134a/CF 3 I as 63 %/9%/28% on a weight basis.
- thermodynamic properties of the mixtures have been calculated as follows.
- Literature values of the properties of R- 134a and CF 3 I were used.
- the properties for R-134a were taken from the REFPROP7.0 program supplied by the National Institute for Standards and Technology (NIST).
- the properties of CF 3 I were obtained from the MST Web book website (http ://webbook.nist. gov) and from the academic literature, in particular from Duan et al Fluid Phase Equilibria (1996) vl21 pp227-234 and J Chem EngData (1999) v44 p ⁇ 501-504.
- R-1234yf saturated liquid vapour pressure and liquid density have been measured.
- the vapour pressure has been used to determine the acentric factor for R-1234yf.
- the boiling point for R-1234)'f and its chemical structure, have been used to estimate the ideal gas enthalpy of R-1234yf by using Joback's estimation method, which is described in more detail in the textbook "The Properties of Gases and Liquids" 4th edition, editors RC Reid, JM Prausnitz, BE Poling, published by McGraw- Hill 1987.
- the critical temperature, critical pressure and the calculated acentric factor data have been used in conjunction with the Peng Robinson equation of state to generate estimates of vapour pressure data for the fluid over the range of temperatures -50 0 C to the critical point. These predicted vapour pressures agreed closely with the observed data, which were measured over the range -20 to +-6O 0 C 3 giving confidence that this equation of state can adequately predict vapour pressure for the temperature range of interest.
- the Peng Robinson equation of state has been used in conjunction with the estimated ideal gas heat capacity to calculate the density, enthalpy and entropy of the real gas, and to estimate the latent heat of vaporisation from use of the Clapeyron relationship between vapour pressure and the difference in volume between saturated liquid and saturated vapour.
- the Peng Robinson equation has also been used to determine the phase equilibrium behaviour of the mixtures.
- the binary interaction constants that are used by this equation to correlate vapour-liquid equilibrium between pairs of fluids were determined as follows. For R-1234yf with CF 3 I 5 boiling point data for mixtures of the two fluids contained in US Patent Application US2005/0233934A1 were used to estimate the interaction constant. For the other interactions (those concerning R-134a) the constants were set to zero.
- the volumetric capacity of the ternary mixture comprising R-1234yf/R- 134a/CF 3 I is equivalent to that of the binary composition comprising R-1234yf/CF 3 I (71%/29% weight basis).
- the compressor displacement required to deliver a given rate of cooling is equivalent for both blends.
- the energy efficiency of the ternary mixture is enhanced (102%) compared to the binary mixture of R-1234yf and CF 3 I, representing an additional benefit to the invention.
- the temperature glide (difference between dewpoint temperature and bubblepoint temperature of the mixture at 1 atmosphere pressure) is negligible for both mixtures, indicating that the ternary mixture is azeotrope-like.
- the GWP of the ternary mixture calculated assigning a GWP of 10 to the tetrafluoropropene, is 123, which is less than 150 and therefore suitable for certain applications such as automotive air conditioning systems.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
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Abstract
A heat transfer composition comprising (i) at least one flammable component selected from R-1234yf and R-152a, (ii) CF3I, and (iii) at least one non-flammable (hydro)fluorocarbon, wherein the composition has a GWP of less than that of the at least one non flammable (hydro)fluorocarbon. Preferably, the at least one non-flammable (hydro)fluorocarbon is selected from R-134a, R-134, R-125, R-245fa, R- 245ca, R-245cb, R-236fa and R-227ea.
Description
HEAT TRANSFER COMPOSITIONS
The invention relates to heat transfer compositions, and in particular to heat transfer compositions comprising at least one flammable component.
Mechanical refrigeration systems (and related heat transfer devices such as heat pumps and air-conditioning systems) are well known. In such systems, a refrigerant liquid evaporates at low pressure taking heat from the surrounding zone. The resulting vapour is then compressed and passed to a condenser where it condenses and gives off heat to a second zone, the condensate being returned through an expansion valve to the evaporator, so completing the cycle. Mechanical energy required for compressing the vapour and pumping the liquid is provided by, for example, an electric motor or an internal combustion engine.
In addition to having a suitable boiling point and a high latent heat of vaporisation, the properties preferred in a refrigerant include low toxicity, non-flammability, non-corrosivity, high stability and freedom from objectionable odour. Other desirable properties are ready compressibility at pressures below 25 bars, low discharge temperature on compression, high refrigeration capacity, high efficiency (high coefficient of performance) and an evaporator pressure in excess of 1 bar at the desired evaporation temperature.
Dichlorodifluoromethane (refrigerant R- 12) possesses a suitable combination of properties and was for many years the most widely used refrigerant. Due to international concern that fully and partially halogenated chlorofluorocarbons, such as dichlorodifluoromethane and chlorodifluoromethane, were damaging the earth's protective ozone layer, there was general agreement that their manufacture and use should be
severely restricted and eventually phased out completely. The use of dichlorofiuoromethane was phased out in the 1990's.
1,1,1,2-tetrafluoroethane (refrigerant R- 134a) was introduced as a replacement refrigerant for R-12. However, despite having a low ozone depletion potential, R-134a has a global warming potential (GWP) of 1300.
Whilst heat transfer devices of the type to which the present invention relates are essentially closed systems, loss of refrigerant to the atmosphere can occur due to leakage during operation of the equipment or during maintenance procedures. It is important, therefore, to replace fully and partially halogenated chlorofluorocarbon refrigerants by materials having zero ozone depletion potentials.
In addition to the possibility of ozone depletion, it has been suggested that significant concentrations of halocarbon refrigerants in the atmosphere might contribute to global warming (the so-called greenhouse effect). It is desirable, therefore, to use refrigerants which have relatively short atmospheric lifetimes as a result of their ability to react with other atmospheric constituents such as hydroxyl radicals or as a result of ready degradation through photolytic processes.
There is a need to provide alternative refrigerants having improved properties, such as low fiammability. There is also a need to provide alternative refrigerants that may be used in existing devices such as refrigeration devices with little or no modification.
In accordance with one aspect of the invention, there is provided a heat transfer composition comprising
(i) at least one flammable component selected from R-1234yf and R- 152a,
(ii) CF3I5 and
(iii) at least one non-flammable (hydro)fluorocarbon, wherein the composition has a GWP of less than that of the at least one nonflammable (hydro)fluorocarbon.
"PreferabTy7tEe"composltion'comprises substantially no R--12-34yf÷
Conveniently, the composition comprises substantially no R-152a.
Advantageously, the at least one non-flammable, (hydro)fluorocarbon is selected from R-134a, R-134, R-125, R-245fa, R-245ca, R-245cb, R-236fa and R-227ea.
Preferably, the at least one (hydro)fluorocarbon is selected from R- 134a and R-245fa.
Conveniently, the composition comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about 30% by weight of the composition.
Advantageously, the composition comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about 10% by weight of the composition.
Preferably, the composition comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about 6% by weight of the composition.
Advantageously, the composition comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about 5% by weight of the composition.
Preferably, the composition is azeotrope-like.
Conveniently, the composition has a GWP of about 750 or less.
Advantageously, the composition has a GWP of about 500 or less.
Preferably, the composition has a GWP of about 250 or less.
Conveniently, the composition has a GWP of about 150 or less.
Advantageously, the composition has a GWP of about 100 or less.
Preferably, the composition further comprises a lubricant.
Conveniently, the lubricant is selected from the group consisting of mineral oil, silicone oil, polyalkyl benzenes (PABs)5 polyol esters (POEs), polyalkylene glycols (PAGs), polyalkylene glycol esters (PAG esters), polyvinyl ethers (PVEs), poly (alpha-olefms) and combinations thereof.
Advantageously, the composition further comprises a stabiliser.
Preferably, the stabiliser is selected from the group consisting of diene- based compounds, phosphates, phenol compounds and epoxides, and mixtures thereof.
Conveniently, the composition further comprises an additional flame retardant.
Advantageously, the additional flame retardant is selected from the group consisting of tri-(2-chloroethyl)-phosphate, (chloropropyl)phosphate, tri-
(2,3 -dibromopropyl)-phosphate, tri-( 1 ,3 -dichloropropyl)-phosphate, diammonium phosphate, various halogenated aromatic compounds, antimony oxide, aluminium trihydrate, polyvinyl chloride, a fluorinated iodocarbon, a fluorinated bromocarbon, trifluoroiodomethane, perfiuoroalkyl amines, bromo-fluoroalkyl amines and mixtures thereof.
Preferably, the composition is a refrigerant composition.
According to another aspect of the invention, there is provided a heat transfer device containing a composition of the invention.
Preferably, the heat transfer device is a refrigeration device.
Conveniently, the heat transfer device is selected from group consisting of automotive air conditioning systems, residential air conditioning S3fstems, commercial air conditioning systems, residential refrigerator systems, residential freezer systems, commercial refrigerator systems, commercial freezer systems, chiller air conditioning systems, chiller refrigeration systems, heat pump systems.
Advantageously, the heat transfer device contains a centrifugal-type compressor.
According to a further aspect of the invention, there is provided a blowing agent comprising a composition of the invention.
According to another aspect of the invention, there is provided a foamable composition comprising one or more components capable of forming foam and a composition of the invention.
Preferably, the one or more components capable of forming foam are selected from polyurethanes, thermoplastic polymers and resins, such as polystyrene, and epoxy resins.
According to a further aspect of the invention, there is provided a foam obtainable from the foamable composition of the invention.
Preferably the foam comprises a composition of the invention.
According to another aspect of the invention, there is provided a sprayable composition comprising a material to be sprayed and a propellant comprising a composition of the invention.
According to a further aspect of the invention, there is provided a method for cooling an article which comprises condensing a composition of the invention and thereafter evaporating said composition in the vicinity of the article to be cooled.
According to another aspect of the invention, there is provided a method for heating an article which comprises condensing a composition of the invention in the vicinity of the article to be heated and thereafter evaporating said composition.
According to a further aspect of the invention, there is provided a method for extracting a substance from biomass comprising contacting the biomass
with a solvent comprising a composition of the invention, and separating the substance from the solvent.
According to another aspect of the invention, there is provided a method of cleaning an article comprising contacting the article with a solvent comprising a composition of the invention.
According to a further aspect of the invention, there is provided a method for extracting a material from an aqueous solution comprising contacting the aqueous solution with a solvent comprising a composition of the invention, and separating the substance from the solvent.
According to another aspect of the invention, there is provided a method for extracting a material from a particulate solid matrix comprising contacting the particulate solid matrix with a solvent comprising a composition of the invention, and separating the substance from the solvent.
According to a further aspect of the invention, there is provided a mechanical power generation device containing a composition of the invention.
Preferably, the mechanical power generation device is adapted to use a Rankine Cycle or modification thereof to generate work from heat.
According to another aspect of the invention, there is provided a method of retrofitting a refrigeration device comprising the step of removing an existing heat transfer fluid, and introducing a composition of the invention.
s mentioned above, due to concerns about potentially harmful environmental effects of existing heat transfer compositions, there is an on-
going trend towards the use of fluids which have an improved (i.e. lower) global warming potential (GWP). However, although fluids which have been proposed to replace traditional heat transfer fluids may have a reduced GWP5 many of them have increased flammability.
It is known to include in heat transfer compositions substances which reduce the flammability of the composition. For example, trifhioroiodomethane (CF3I) has been proposed for use as a flame retardant in heat transfer compositions. However, CF3I has a number of disadvantages. Firstly, CF3I is relatively expensive, partly due to the relative scarcity of the element iodine. Also, CF3I has a high molecular weight of 195.91. In practice, this means that a relatively large and expensive amount of CF3I must be combined with a flammable heat transfer fluid in order to result in significantly reduced flammability. Also, the use of such relatively high amounts of CF3I can lead to increased weight of fluid to be used in a heat transfer device, such as an automotive air- conditioning system, as compared to a traditional heat transfer composition.
We have unexpectedly found that blending a non-flammable (hydro)fluorocarbon fluid with a flammable (hydro)fluorocarbon fluid and CF3I can result in a composition having an acceptable GWP and an acceptable flammability. In particular, the use of at least one nonflammable (hydro)fluorocarbon fluid with a relatively high GWP can result in a heat transfer composition of reduced flammability and acceptable GWP. Also, the level of CF3I needed to give the required level of non- flammability can be reduced.
In some circumstances, it is preferred for the compositions to have a GWP of about 150 or less. However, for other applications, it may be acceptable
for composition to have a higher GWP, for example a GWP of up to 250, 500 or 750.
Preferred flammable refrigerants are 2,3,3,3-tetrafluoropropene (R-1234yf) and 1,1-difmoroethane (R-152a).
Preferred non-flammable (hydro)fluorocarbon fluids are R- 134a, R- 134, R- 125, R-245fa, R-245ca, R-245cb, R-236fa andR-227ea.
The non-flammable (hydro)fluorocarbon components may be present in the composition preferably in a range from about 1 to about 30% by weight. The maximum proportion preferred for any given application will be determined by the fluid's Greenhouse Warming Potential (GWP) and the desired GWP of the formulated blend of flammable fluid, CF3I and non- flammable fluid.
Typical but non-limiting preferred ranges for specific non-flammable fluids (by % weight) are set out below:
The flammability of R-1234yf when mixed with air and CF3I has been determined according to the methodology of Addendum p to ASHRAE Standard 34, using the ASTM E681 protocol in a 12 litre flask with electronic ignition. The test temperature used was 600C and the humidity was equivalent to 50% relative humidity at 230C.
The flammability limits of R-1234yf in air were found to be 5.5% to 13.4% v/v. The minimum quantity of CF3I required to render the fuel nonflammable in air at all concentrations was found to be 19% v/v when mixed with R-1234yf.
The test was repeated, using as fuel a mixture of R-1234yf with R-134a in the molar ratio 86:14. The flammability limits of this fuel mixture in air were found to be 6.5% to 15% v/v. The minimum quantity of CF3I required to render the fuel non-flammable in air at all concentrations was found to be 18% v/v.
Thermodynamic Property Estimation
The key thermodynamic properties of a fluid for estimation of its performance as a refrigerant or air conditioning system working fluid are:
• The critical temperature - the highest temperature at which liquid and vapour phases can co-exist. • The vapour pressure of the fluid over the temperature range of operation of the refrigerant/air conditioning equipment. ® The latent heat of vaporisation of the fluid, β The variation of the gas density with pressure and temperature
• The heat capacity of the gas and liquid states. Two mixtures have been studied. The first mixture is a binary mixture of R- 1234yf with CF3I, such that the quantity Of CF3I in the mixture is sufficient to render the mixture non-flammable in air at all concentrations according to the flammability test data determined above. This yields a mixture composition of R-1234yf/CF3I as 71%/29% on a weight basis.
The above binary mixture was compared with a ternary mixture of the invention, comprising R-1234yf/R-134a/CF3I, selected such that the molar ratio of R-1234yf:R-134a is 86:14 and the mixture is non-flammable in air at all concentrations. This }άelds a mixture composition of R-1234yf/R- 134a/CF3I as 63 %/9%/28% on a weight basis.
The thermodynamic properties of the mixtures have been calculated as follows. Literature values of the properties of R- 134a and CF3I were used. The properties for R-134a were taken from the REFPROP7.0 program supplied by the National Institute for Standards and Technology (NIST). The properties of CF3I were obtained from the MST Web book website (http ://webbook.nist. gov) and from the academic literature, in particular from Duan et al Fluid Phase Equilibria (1996) vl21 pp227-234 and J Chem EngData (1999) v44 pρ501-504.
For R-1234yf the critical point, saturated liquid vapour pressure and liquid density have been measured. The vapour pressure has been used to determine the acentric factor for R-1234yf. The boiling point for R-1234)'f and its chemical structure, have been used to estimate the ideal gas enthalpy of R-1234yf by using Joback's estimation method, which is described in more detail in the textbook "The Properties of Gases and Liquids" 4th edition, editors RC Reid, JM Prausnitz, BE Poling, published by McGraw- Hill 1987.
The critical temperature, critical pressure and the calculated acentric factor data have been used in conjunction with the Peng Robinson equation of state to generate estimates of vapour pressure data for the fluid over the range of temperatures -500C to the critical point. These predicted vapour pressures agreed closely with the observed data, which were measured over the range -20 to +-6O0C3 giving confidence that this equation of state can
adequately predict vapour pressure for the temperature range of interest. The Peng Robinson equation of state has been used in conjunction with the estimated ideal gas heat capacity to calculate the density, enthalpy and entropy of the real gas, and to estimate the latent heat of vaporisation from use of the Clapeyron relationship between vapour pressure and the difference in volume between saturated liquid and saturated vapour. The Peng Robinson equation has also been used to determine the phase equilibrium behaviour of the mixtures. The binary interaction constants that are used by this equation to correlate vapour-liquid equilibrium between pairs of fluids were determined as follows. For R-1234yf with CF3I5 boiling point data for mixtures of the two fluids contained in US Patent Application US2005/0233934A1 were used to estimate the interaction constant. For the other interactions (those concerning R-134a) the constants were set to zero.
The refrigeration performance of the two mixtures was compared using a standard idealised air conditioning cycle calculation as discussed below. An idealised vapour compression cycle, consisting of four steps as outlined below, was used to perform the calculations necessary to provide these evaluation parameters:
(a) Isothermal evaporation of a refrigerant liquid at constant temperature followed by warming of the vapour to ambient temperature.
(b) Compression of the refrigerant vapour in a positive displacement compressor of specified isentropic efficiency and clearance volume.
(c) Cooling and condensation of the vapour to liquid with the average condensation temperature and the final liquid temperature specified.
(d) Throttling of the liquid refrigerant from condenser to evaporator pressure to complete the cycle.
The conditions used are typical of a mobile air conditioning (MAC) application and are as follows for all fluids:
• Evaporation temperature: 5DC. • Temperature of the vapour at the inlet to the compressor: 250C.
• Condensation temperature of the vapour: 450C.
• Compressor isentropic efficiency: 65%.
• Compressor clearance volume: 4%.
The volumetric capacity of the ternary mixture comprising R-1234yf/R- 134a/CF3I (composition 63%/9%/28% weight basis) is equivalent to that of the binary composition comprising R-1234yf/CF3I (71%/29% weight basis). In other words, the compressor displacement required to deliver a given rate of cooling is equivalent for both blends.
The energy efficiency of the ternary mixture is enhanced (102%) compared to the binary mixture of R-1234yf and CF3I, representing an additional benefit to the invention. The temperature glide (difference between dewpoint temperature and bubblepoint temperature of the mixture at 1 atmosphere pressure) is negligible for both mixtures, indicating that the ternary mixture is azeotrope-like.
The GWP of the ternary mixture, calculated assigning a GWP of 10 to the tetrafluoropropene, is 123, which is less than 150 and therefore suitable for certain applications such as automotive air conditioning systems.
Claims
1. A heat transfer composition comprising
(i) at least one flammable component selected from R-1234yf and R- 152a,
(ii) CF3I, and
(iii) at least one non-flammable (hydro)fluorocarbon, wherein the composition has a GWP of less than that of the at least one nonflammable (hydro)fhiorocarbon.
2. A composition according to Claim 1 which comprises substantially no R-1234yf.
3. A composition according to Claim 1 which comprises substantially no R- 152a.
4. A composition according to any preceding claim wherein the at least one non-flammable (hydro)fiuorocarbon is selected from R-134a, R-134, R- 125, R-245fa, R-245ca, R-245cb, R-236fa and R-227ea.
5. A composition according to Claim 4 wherein the at least one (hydro)fluorocarbon is selected from R-134a and R-245fa.
6. A composition according to any preceding claim which comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about
30% by weight of the composition.
7. A composition according to any preceding claim which comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about 10% by weight of the composition.
8. A composition according to any preceding claim, which comprises the at least one (hydro)fluorocarbon in an amount of from about 1 to about 6% by weight of the composition.
9. A composition according to any preceding claim which comprises the at least one (hydro)fiuorocarbon in an amount of from about 1 to about 5% by weight of the composition.
10. A composition according to any preceding claim which is azeotrope- like.
11. A composition according to any preceding claims which has a GWP of about 750 or less.
12. A composition according to any preceding claims which has a GWP of about 500 or less.
13. A composition according to any preceding claims which has a GWP of about 250 or less.
14. A composition according to any preceding claims which has a GWP of about 150 or less.
15. A composition according to any preceding claims which has a GWP of about 100 or less.
16. A composition according to an)' preceding claim further comprising a lubricant.
17. A composition according to Claim 16 wherein the lubricant is selected from the group consisting of mineral oil, . silicone oil, polyalkyl benzenes (PABs), polyol esters (POEs)3 polyalkylene glycols (PAGs)5 polyalkylene glycol esters (PAG esters), polyvinyl ethers (PVEs)5 poly
5 (alpha-olefϊns) and combinations thereof.
18. A composition according to any preceding claim further comprising a stabiliser.
io 19. A composition according to Claim 18 wherein the stabiliser is selected from the group consisting of diene-based compounds, phosphates, phenol compounds and epoxides, and mixtures thereof.
20. A composition according to any preceding claim further comprising ■ 15 an additional flame retardant.
21. A composition according to Claim 20 wherein the additional flame retardant is selected from the group consisting of tri-(2-chloroethyl)- phosphate, (chloropropyl)phosphate, tri-(2,3-dibromopropyl)-phosphate, tri-
20 (l,3-dichloropropyl)-phosphate, diammonium phosphate, various halogenated aromatic compounds, antimony oxide, aluminium trihydrate, polyvinyl chloride, a fluorinated iodocarbon, a fluorinated bromocarbon, trifluoroiodomethane, perfluoroalkyl amines, bromo-fluoroalkyl amines and mixtures thereof.
25
22. A composition according to any preceding claim which is a refrigerant composition.
23. A heat transfer device containing a composition as defined any of 30 Claims 1 to 21.
24. A heat transfer device according to Claim 23 which is a refrigeration device.
25. A heat transfer device according to Claim 24 which is selected from group consisting of automotive air conditioning systems, residential air conditioning systems, commercial air conditioning systems, residential refrigerator systems, residential freezer systems, commercial refrigerator systems, commercial freezer systems, chiller air conditioning systems, chiller refrigeration systems, heat pump systems.
26. A heat transfer device according to Claim 24 or 25 which contains a centrifugal-type compressor.
27. A blowing agent comprising a composition as defined in any of Claims l to 21.
28. A foamable composition comprising one or more components capable of forming foam and a composition as defined in any of Claims 1 to 21.
29. A foamable composition according to Claim 28 wherein the one or more components capable of forming foam are selected from polyurethanes, thermoplastic polymers and resins, such as polystyrene, and epoxy resins.
30. A foam obtainable from the foamable composition of Claim 28 or 29.
31. A foam according to Claim 30 comprising a composition as defined in any of Claims 1 to 21.
32. A sprayable composition comprising a material to be sprayed and a propellant comprising a composition as defined in any of Claims 1 to 21.
33. A method for cooling an article which comprises condensing a composition as defined in any of Claims 1 to 21 and thereafter evaporating said composition in the vicinity of the article to be cooled.
34. A method for heating an article which comprises condensing a composition as defined in any of Claims 1 to 21 in the vicinity of the article to be heated and thereafter evaporating said composition.
35. A method for extracting a substance from biomass comprising contacting the biomass with a solvent comprising a composition as defined in any of Claims 1 to 21, and separating the substance from the solvent.
36. A method of cleaning an article comprising contacting the article with a solvent comprising a composition as defined in any of Claims 1 to 21.
37. A method for extracting a material from an aqueous solution comprising contacting the aqueous solution with a solvent comprising a composition as defined in any of Claims 1 to 21, and separating the substance from the solvent.
38. A method for extracting a material from a particulate solid matrix comprising contacting the particulate solid matrix with a solvent comprising a composition as defined in any of Claims 1 to 21, and separating the substance from the solvent.
39. A mechanical power generation device containing a composition as defined in an}' of Claims 1 to 21.
40. A mechanical power generation device according to Claim 39 which 5 is adapted to use a Rankine Cycle or modification thereof to generate work from heat.
41. A method of retrofitting a refrigeration device comprising the step of removing an existing heat transfer fluid, and introducing a composition as l o defined in any of Claim 1 to 21.
42. A heat transfer composition substantially as hereinbefore described.
Applications Claiming Priority (2)
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GB0612485A GB2439392A (en) | 2006-06-23 | 2006-06-23 | Heat transfer compositions |
GB0612485.3 | 2006-06-23 |
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WO2007148046A1 true WO2007148046A1 (en) | 2007-12-27 |
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PCT/GB2007/002174 WO2007148046A1 (en) | 2006-06-23 | 2007-06-12 | Heat transfer compositions |
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WO (1) | WO2007148046A1 (en) |
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JP2018154841A (en) * | 2008-05-07 | 2018-10-04 | ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー | Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene |
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CN111040734A (en) * | 2019-12-30 | 2020-04-21 | 山东华安新材料有限公司 | HFC-152a refrigerant composition |
CN112867774A (en) * | 2018-10-15 | 2021-05-28 | 霍尼韦尔国际公司 | Azeotrope or azeotrope-like composition of trifluoroiodomethane (CF3I) and 1,1,1,3,3, 3-hexafluoropropane (HFC-236fa) |
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JP2020002370A (en) * | 2008-05-07 | 2020-01-09 | ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー | Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene |
US11001738B2 (en) | 2008-05-07 | 2021-05-11 | The Chemours Company Fc, Llc | Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene |
JP2018154841A (en) * | 2008-05-07 | 2018-10-04 | ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー | Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene |
US10214669B2 (en) * | 2008-05-07 | 2019-02-26 | The Chemours Company Fc, Llc | Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene |
US10584270B2 (en) | 2008-05-07 | 2020-03-10 | The Chemours Company Fc, Llc | Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene |
US11512239B2 (en) | 2008-05-07 | 2022-11-29 | The Chemours Company Fc, Llc | Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene |
US11312890B2 (en) | 2008-05-07 | 2022-04-26 | The Chemours Company Fc, Llc | Compositions comprising 2,3-dichloro-1,1,1 -trifluoropropane, 2-chloro-1,1,1 -trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene |
WO2013032768A1 (en) * | 2011-08-29 | 2013-03-07 | E. I. Du Pont De Nemours And Company | Compositions comprising 1,1,1,2,2-pentafluoropropane and a fluoroolefin and uses thereof |
CN103764737A (en) * | 2011-08-29 | 2014-04-30 | 纳幕尔杜邦公司 | Compositions comprising 1,1,1,2,2-pentafluoropropane and a fluoroolefin and uses thereof |
US9410105B2 (en) | 2012-11-16 | 2016-08-09 | Basf Se | Lubricant compositions comprising epoxide compounds |
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CN109988546A (en) * | 2017-12-29 | 2019-07-09 | 特灵国际有限公司 | Lower GWP refrigerant composition |
US20190203091A1 (en) * | 2017-12-29 | 2019-07-04 | Trane International Inc. | Lower gwp refrigerant compositions |
CN109988546B (en) * | 2017-12-29 | 2023-03-07 | 特灵国际有限公司 | Lower GWP refrigerant compositions |
EP3505588A1 (en) * | 2017-12-29 | 2019-07-03 | Trane International Inc. | Lower gwp refrigerant compositions |
CN112867774A (en) * | 2018-10-15 | 2021-05-28 | 霍尼韦尔国际公司 | Azeotrope or azeotrope-like composition of trifluoroiodomethane (CF3I) and 1,1,1,3,3, 3-hexafluoropropane (HFC-236fa) |
JP7383019B2 (en) | 2018-10-15 | 2023-11-17 | ハネウェル・インターナショナル・インコーポレーテッド | Azeotrope or azeotrope-like composition of trifluoroiodomethane (CF3I) and 1,1,1,3,3,3-hexafluoropropane (HFC-236fa) |
JP2022505093A (en) * | 2018-10-15 | 2022-01-14 | ハネウェル・インターナショナル・インコーポレーテッド | Azeotrope or azeotrope-like composition of trifluoroiodomethane (CF3I) and 1,1,1,3,3,3-hexafluoropropane (HFC-236fa) |
CN111040734A (en) * | 2019-12-30 | 2020-04-21 | 山东华安新材料有限公司 | HFC-152a refrigerant composition |
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GB0612485D0 (en) | 2006-08-02 |
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