MX2011005211A - Composiciones de tetrafluoropropeno y sus usos. - Google Patents
Composiciones de tetrafluoropropeno y sus usos.Info
- Publication number
- MX2011005211A MX2011005211A MX2011005211A MX2011005211A MX2011005211A MX 2011005211 A MX2011005211 A MX 2011005211A MX 2011005211 A MX2011005211 A MX 2011005211A MX 2011005211 A MX2011005211 A MX 2011005211A MX 2011005211 A MX2011005211 A MX 2011005211A
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- MX
- Mexico
- Prior art keywords
- hfc
- weight percent
- hfo
- composition
- compositions
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 346
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 title abstract description 16
- 238000001816 cooling Methods 0.000 claims abstract description 37
- 238000000034 method Methods 0.000 claims abstract description 34
- 238000005057 refrigeration Methods 0.000 claims abstract description 33
- 238000004378 air conditioning Methods 0.000 claims abstract description 28
- 230000008569 process Effects 0.000 claims abstract description 12
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims description 210
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 claims description 110
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims description 109
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 claims description 94
- 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 claims description 55
- 239000000314 lubricant Substances 0.000 claims description 42
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 claims description 33
- 150000001875 compounds Chemical class 0.000 claims description 21
- 238000001704 evaporation Methods 0.000 claims description 10
- 230000008020 evaporation Effects 0.000 claims description 10
- 239000002480 mineral oil Substances 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 5
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 5
- 230000005494 condensation Effects 0.000 claims description 5
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 4
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 4
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- 229920013639 polyalphaolefin Polymers 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 229920001296 polysiloxane Polymers 0.000 claims description 3
- 229920001289 polyvinyl ether Polymers 0.000 claims description 3
- 150000004760 silicates Chemical class 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 abstract description 10
- 239000012530 fluid Substances 0.000 abstract description 6
- 239000004604 Blowing Agent Substances 0.000 abstract description 3
- 239000006260 foam Substances 0.000 abstract description 3
- 239000003380 propellant Substances 0.000 abstract description 3
- 230000001629 suppression Effects 0.000 abstract description 2
- 239000003507 refrigerant Substances 0.000 description 82
- -1 butane or propane Chemical class 0.000 description 35
- 239000007788 liquid Substances 0.000 description 21
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 20
- 239000000126 substance Substances 0.000 description 17
- 230000008859 change Effects 0.000 description 15
- 239000000654 additive Substances 0.000 description 14
- 239000000975 dye Substances 0.000 description 13
- 239000000700 radioactive tracer Substances 0.000 description 13
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 12
- 238000010792 warming Methods 0.000 description 12
- 239000007789 gas Substances 0.000 description 11
- 229930195733 hydrocarbon Natural products 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 239000003921 oil Substances 0.000 description 9
- 239000010702 perfluoropolyether Substances 0.000 description 9
- 150000002430 hydrocarbons Chemical class 0.000 description 8
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 7
- 229910019142 PO4 Inorganic materials 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 7
- 238000009835 boiling Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 235000021317 phosphate Nutrition 0.000 description 7
- 239000003381 stabilizer Substances 0.000 description 7
- 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 6
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 6
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 6
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 6
- 239000001282 iso-butane Substances 0.000 description 6
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 6
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical class [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 230000006835 compression Effects 0.000 description 5
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- 238000001914 filtration Methods 0.000 description 5
- 239000013529 heat transfer fluid Substances 0.000 description 5
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- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical class OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 4
- 229920001774 Perfluoroether Polymers 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 4
- 239000002826 coolant Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 150000002576 ketones Chemical class 0.000 description 4
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical group C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 3
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- 150000002118 epoxides Chemical class 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 239000007850 fluorescent dye Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000002608 ionic liquid Substances 0.000 description 3
- 150000002596 lactones Chemical class 0.000 description 3
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- 238000005461 lubrication Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
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- 230000009467 reduction Effects 0.000 description 3
- 150000003568 thioethers Chemical class 0.000 description 3
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 2
- UNMJLQGKEDTEKJ-UHFFFAOYSA-N (3-ethyloxetan-3-yl)methanol Chemical compound CCC1(CO)COC1 UNMJLQGKEDTEKJ-UHFFFAOYSA-N 0.000 description 2
- YFMFNYKEUDLDTL-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)C(F)(F)F YFMFNYKEUDLDTL-UHFFFAOYSA-N 0.000 description 2
- LKUDPHPHKOZXCD-UHFFFAOYSA-N 1,3,5-trimethoxybenzene Chemical compound COC1=CC(OC)=CC(OC)=C1 LKUDPHPHKOZXCD-UHFFFAOYSA-N 0.000 description 2
- OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 description 2
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 2
- RFCAUADVODFSLZ-UHFFFAOYSA-N 1-Chloro-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)(F)C(F)(F)Cl RFCAUADVODFSLZ-UHFFFAOYSA-N 0.000 description 2
- IQQRAVYLUAZUGX-UHFFFAOYSA-N 1-butyl-3-methylimidazolium Chemical compound CCCCN1C=C[N+](C)=C1 IQQRAVYLUAZUGX-UHFFFAOYSA-N 0.000 description 2
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 2
- BVUXDWXKPROUDO-UHFFFAOYSA-N 2,6-di-tert-butyl-4-ethylphenol Chemical compound CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BVUXDWXKPROUDO-UHFFFAOYSA-N 0.000 description 2
- AQZRARFZZMGLHL-UHFFFAOYSA-N 2-(trifluoromethyl)oxirane Chemical compound FC(F)(F)C1CO1 AQZRARFZZMGLHL-UHFFFAOYSA-N 0.000 description 2
- SZAQZZKNQILGPU-UHFFFAOYSA-N 2-[1-(2-hydroxy-3,5-dimethylphenyl)-2-methylpropyl]-4,6-dimethylphenol Chemical compound C=1C(C)=CC(C)=C(O)C=1C(C(C)C)C1=CC(C)=CC(C)=C1O SZAQZZKNQILGPU-UHFFFAOYSA-N 0.000 description 2
- HXIQYSLFEXIOAV-UHFFFAOYSA-N 2-tert-butyl-4-(5-tert-butyl-4-hydroxy-2-methylphenyl)sulfanyl-5-methylphenol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1SC1=CC(C(C)(C)C)=C(O)C=C1C HXIQYSLFEXIOAV-UHFFFAOYSA-N 0.000 description 2
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
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- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
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- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
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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
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D1/00—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
- A62D1/0028—Liquid extinguishing substances
- A62D1/0057—Polyhaloalkanes
-
- 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
- C09K3/00—Materials not provided for elsewhere
- C09K3/30—Materials not provided for elsewhere for aerosols
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
- C09K5/041—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
- C09K5/044—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
- C09K5/045—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds containing only fluorine as halogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/10—Components
- C09K2205/12—Hydrocarbons
- C09K2205/122—Halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/10—Components
- C09K2205/12—Hydrocarbons
- C09K2205/126—Unsaturated fluorinated hydrocarbons
-
- 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
- C09K2205/32—The mixture being azeotropic
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Thermal Sciences (AREA)
- Combustion & Propulsion (AREA)
- Physics & Mathematics (AREA)
- Emergency Management (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Business, Economics & Management (AREA)
- General Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fire-Extinguishing Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11602908P | 2008-11-19 | 2008-11-19 | |
| US18020109P | 2009-05-21 | 2009-05-21 | |
| PCT/US2009/064921 WO2010059677A2 (en) | 2008-11-19 | 2009-11-18 | Tetrafluoropropene compositions and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2011005211A true MX2011005211A (es) | 2011-06-01 |
Family
ID=41565982
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2011005211A MX2011005211A (es) | 2008-11-19 | 2009-11-18 | Composiciones de tetrafluoropropeno y sus usos. |
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| JP (2) | JP5689068B2 (cg-RX-API-DMAC7.html) |
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| CN (2) | CN104726066A (cg-RX-API-DMAC7.html) |
| AR (1) | AR074381A1 (cg-RX-API-DMAC7.html) |
| AU (3) | AU2009316668B2 (cg-RX-API-DMAC7.html) |
| BR (2) | BR122013002802A2 (cg-RX-API-DMAC7.html) |
| CA (2) | CA2741871C (cg-RX-API-DMAC7.html) |
| DE (2) | DE202009019199U1 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2556762T5 (cg-RX-API-DMAC7.html) |
| MX (1) | MX2011005211A (cg-RX-API-DMAC7.html) |
| WO (1) | WO2010059677A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (118)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8974688B2 (en) * | 2009-07-29 | 2015-03-10 | Honeywell International Inc. | Compositions and methods for refrigeration |
| GB201002625D0 (en) * | 2010-02-16 | 2010-03-31 | Ineos Fluor Holdings Ltd | Heat transfer compositions |
| US8512591B2 (en) | 2007-10-12 | 2013-08-20 | Mexichem Amanco Holding S.A. De C.V. | Heat transfer compositions |
| US8628681B2 (en) | 2007-10-12 | 2014-01-14 | Mexichem Amanco Holding S.A. De C.V. | Heat transfer compositions |
| US8333901B2 (en) | 2007-10-12 | 2012-12-18 | Mexichem Amanco Holding S.A. De C.V. | Heat transfer compositions |
| US9546311B2 (en) | 2008-08-19 | 2017-01-17 | Honeywell International Inc. | Azeotrope-like compositions of 1,1,1,2-tetrafluoropropene and 1,1,1,2-tetrafluoroethane |
| FR2936806B1 (fr) | 2008-10-08 | 2012-08-31 | Arkema France | Fluide refrigerant |
| US20100122545A1 (en) | 2008-11-19 | 2010-05-20 | E. I. Du Pont De Nemours And Company | Tetrafluoropropene compositions and uses thereof |
| PT2427527E (pt) | 2009-05-08 | 2016-02-11 | Honeywell Int Inc | Composições e métodos de transferência de calor |
| CA2761478C (en) * | 2009-05-08 | 2017-09-19 | Samuel F. Yana Motta | Hydrofluorocarbon refrigerant compositions for heat pump water heaters |
| US9845419B2 (en) * | 2009-07-29 | 2017-12-19 | Honeywell International Inc. | Low GWP heat transfer compositions containing difluoromethane and 1,3,3,3-tetrafluoropropene |
| GB0915004D0 (en) * | 2009-08-28 | 2009-09-30 | Ineos Fluor Holdings Ltd | Heat transfer composition |
| US9074115B2 (en) | 2009-08-28 | 2015-07-07 | Mexichem Amanco Holding S.A. De C.V. | Heat transfer compositions |
| FR2950066B1 (fr) | 2009-09-11 | 2011-10-28 | Arkema France | Refrigeration basse et moyenne temperature |
| FR2950068B1 (fr) | 2009-09-11 | 2012-05-18 | Arkema France | Procede de transfert de chaleur |
| FR2950065B1 (fr) | 2009-09-11 | 2012-02-03 | Arkema France | Fluide refrigerant binaire |
| FR2950070B1 (fr) * | 2009-09-11 | 2011-10-28 | Arkema France | Compositions ternaires pour refrigeration haute capacite |
| FR2950069B1 (fr) | 2009-09-11 | 2011-11-25 | Arkema France | Utilisation de compositions ternaires |
| FR2950071B1 (fr) * | 2009-09-11 | 2012-02-03 | Arkema France | Compositions ternaires pour refrigeration basse capacite |
| US10035938B2 (en) | 2009-09-11 | 2018-07-31 | Arkema France | Heat transfer fluid replacing R-134a |
| FR2954342B1 (fr) | 2009-12-18 | 2012-03-16 | Arkema France | Fluides de transfert de chaleur a inflammabilite reduite |
| RU2012131163A (ru) * | 2009-12-21 | 2014-01-27 | Е.И.Дюпон Де Немур Энд Компани | Композиции, содержащие тетрафторпропен и дифторметан, и их применение |
| KR20120075478A (ko) * | 2010-01-27 | 2012-07-06 | 다이킨 고교 가부시키가이샤 | 디플루오로메탄(hfc32) 및 2,3,3,3-테트라플루오로프로펜(hfo1234yf)을 포함하는 냉매 조성물 |
| GB201002619D0 (en) * | 2010-02-16 | 2010-03-31 | Ineos Fluor Holdings Ltd | Heat transfer compositions |
| GB201002622D0 (en) | 2010-02-16 | 2010-03-31 | Ineos Fluor Holdings Ltd | Heat transfer compositions |
| FR2957083B1 (fr) | 2010-03-02 | 2015-12-11 | Arkema France | Fluide de transfert de chaleur pour compresseur centrifuge |
| MX346315B (es) | 2010-04-16 | 2017-03-15 | Du Pont | Composicion que comprende 2, 3, 3, 3,-tetrafluoropropeno y 1, 1, 1, 2-tetrafluoroetano, enfriadores que los contienen y metodos para producir enfriamiento en ellos. |
| FR2959997B1 (fr) | 2010-05-11 | 2012-06-08 | Arkema France | Fluides de transfert de chaleur et leur utilisation dans des echangeurs de chaleur a contre-courant |
| FR2959998B1 (fr) * | 2010-05-11 | 2012-06-01 | Arkema France | Fluides de transfert de chaleur ternaires comprenant du difluoromethane, du pentafluoroethane et du tetrafluoropropene |
| FR2959999B1 (fr) | 2010-05-11 | 2012-07-20 | Arkema France | Fluides de transfert de chaleur et leur utilisation dans des echangeurs de chaleur a contre-courant |
| BR112012029453A2 (pt) | 2010-05-20 | 2017-03-07 | Mexichem Amanco Holding Sa | "composições para transferencia de calor, formação de espuma e pulverizavel, dispositivos para transferencia de calor e para geração de energia mecanica, uso de uma composição, agente para expansão, espuma, e, métodos para esfriar um artigo, para aquecer um artigo, para extrair uma substancia de biomassa, para limpar um artigo, para extrair um material de uma solução aquosa, para extrair um material de uma matriz sólida particulada, para reformar um dispositivo para transferência de calor, para reduzir o impacto ambiental decorrente da operação de um produto, para preparar uma composição e para gerar crédito de emissão de gás de efeito estufa" |
| EP2571954B1 (en) | 2010-05-20 | 2015-12-30 | Mexichem Fluor S.A. de C.V. | Heat transfer compositions |
| CN101851490B (zh) * | 2010-06-04 | 2012-10-24 | 集美大学 | 可替代HFC-134a的制冷剂组合物 |
| MX2012015218A (es) * | 2010-06-22 | 2013-05-17 | Arkema Inc | Composiciones para la transferencia térmica de hidrofluorocarbonos y una hidrofluoroolefina. |
| GB2481443B (en) * | 2010-06-25 | 2012-10-17 | Mexichem Amanco Holding Sa | Heat transfer compositions |
| JP5659403B2 (ja) * | 2010-07-02 | 2015-01-28 | パナソニックIpマネジメント株式会社 | 冷凍サイクル装置 |
| FR2962442B1 (fr) | 2010-07-09 | 2016-02-26 | Arkema France | Composition stable de 2,3,3,3-tetrafluoropropene |
| FR2964977B1 (fr) | 2010-09-20 | 2013-11-01 | Arkema France | Composition a base de 3,3,3-tetrafluoropropene |
| US20120119136A1 (en) * | 2010-11-12 | 2012-05-17 | Honeywell International Inc. | Low gwp heat transfer compositions |
| FR2968009B1 (fr) | 2010-11-25 | 2012-11-16 | Arkema France | Fluides frigorigenes contenant du (e)-1,1,1,4,4,4-hexafluorobut-2-ene |
| CN103228757B (zh) | 2010-11-25 | 2016-02-17 | 阿克马法国公司 | 氯三氟丙烯和六氟丁烯的组合物 |
| FR2968310B1 (fr) | 2010-12-03 | 2012-12-07 | Arkema France | Compositions a base de 1,1,1,4,4,4-hexafluorobut-2-ene et de 3,3,4,4,4-pentafluorobut-1-ene |
| MX344499B (es) | 2010-12-14 | 2016-12-19 | Du Pont | Uso de refrigerantes que comprenden e-1,3,3,3-tetrafluoropropeno y al menos un tetrafluoroetano para enfriamiento. |
| IT1406472B1 (it) | 2010-12-22 | 2014-02-28 | Nuovo Pignone Spa | Prova per similitudine di prestazione di compressore |
| FR2977256B1 (fr) | 2011-07-01 | 2013-06-21 | Arkema France | Compositions de 2,4,4,4-tetrafluorobut-1-ene et de cis-1,1,1,4,4,4-hexafluorobut-2-ene |
| TWI585065B (zh) * | 2011-08-26 | 2017-06-01 | 杜邦股份有限公司 | 含四氟丙烯之組成物及其使用方法 |
| FR2979419B1 (fr) * | 2011-08-30 | 2018-03-30 | Arkema France | Fluides de transfert de chaleur supercritiques a base de tetrafluoropropene |
| JP5941056B2 (ja) | 2011-10-26 | 2016-06-29 | Jxエネルギー株式会社 | 冷凍機用作動流体組成物及び冷凍機油 |
| WO2013122892A1 (en) | 2012-02-13 | 2013-08-22 | E. I. Du Pont De Nemours And Company | Refrigerant mixtures comprising tetrafluoropropene, difluoromethane, pentafluoroethane, and tetrafluoroethane and uses thereof |
| LT2814897T (lt) * | 2012-02-13 | 2018-07-10 | Honeywell International Inc. | Šilumos perdavimo kompozicijos ir būdai |
| KR101874780B1 (ko) | 2012-03-27 | 2018-08-02 | 제이엑스티지 에네루기 가부시키가이샤 | 냉동기용 작동 유체 조성물 |
| JP5977817B2 (ja) * | 2012-03-29 | 2016-08-24 | Jxエネルギー株式会社 | 冷凍機用作動流体組成物 |
| JP5893478B2 (ja) * | 2012-03-30 | 2016-03-23 | 出光興産株式会社 | 冷凍機用潤滑油組成物 |
| JP5972640B2 (ja) * | 2012-03-30 | 2016-08-17 | 出光興産株式会社 | 冷凍機用潤滑油組成物 |
| JP5972639B2 (ja) * | 2012-03-30 | 2016-08-17 | 出光興産株式会社 | 冷凍機用潤滑油組成物 |
| FR2989084B1 (fr) | 2012-04-04 | 2015-04-10 | Arkema France | Compositions a base de 2,3,3,4,4,4-hexafluorobut-1-ene |
| BR112015003635A2 (pt) * | 2012-08-20 | 2017-07-04 | Honeywell Int Inc | composição de troca térmica, método de substituição de um fluido de troca térmica já existente contido no sistema de troca térmica, sistema de troca térmica, e método de transferir calor para ou a partir de um fluido ou corpo. |
| PT2894209T (pt) * | 2012-09-04 | 2022-01-27 | Daikin Ind Ltd | Método para encher mistura refrigerante contendo 2,3,3,3-tetrafluoropropeno |
| FR2998302B1 (fr) | 2012-11-20 | 2015-01-23 | Arkema France | Composition refrigerante |
| US8940180B2 (en) * | 2012-11-21 | 2015-01-27 | Honeywell International Inc. | Low GWP heat transfer compositions |
| FR3000096B1 (fr) * | 2012-12-26 | 2015-02-20 | Arkema France | Composition comprenant du 2,3,3,3-tetrafluoropropene |
| US9982180B2 (en) * | 2013-02-13 | 2018-05-29 | Honeywell International Inc. | Heat transfer compositions and methods |
| CN105189689A (zh) * | 2013-02-25 | 2015-12-23 | 霍尼韦尔国际公司 | 含有二氟甲烷和氟代烯烃的组合物 |
| WO2014143993A1 (en) * | 2013-03-15 | 2014-09-18 | Honeywell International Inc. | Heat transfer compositions and methods |
| CN103194175A (zh) * | 2013-04-22 | 2013-07-10 | 北京工业大学 | 一种用于管式能量回收装置的碳纳米管强化多元制冷剂基换热工质 |
| CN104277765B (zh) | 2013-07-05 | 2017-12-08 | 中化蓝天集团有限公司 | 一种环保型近共沸混合制冷剂 |
| FR3010415B1 (fr) | 2013-09-11 | 2015-08-21 | Arkema France | Fluides de transfert de chaleur comprenant du difluoromethane, du pentafluoroethane, du tetrafluoropropene et eventuellement du propane |
| KR102382714B1 (ko) * | 2013-10-10 | 2022-04-06 | 더 케무어스 컴퍼니 에프씨, 엘엘씨 | 다이플루오로메탄, 펜타플루오로에탄, 테트라플루오로에탄, 및 테트라플루오로프로펜을 포함하는 조성물 및 그의 용도 |
| JP5861727B2 (ja) * | 2014-03-04 | 2016-02-16 | ダイキン工業株式会社 | トランス−1,3,3,3−テトラフルオロプロペンを含む混合冷媒の充填方法 |
| JP2015214632A (ja) * | 2014-05-09 | 2015-12-03 | パナソニックIpマネジメント株式会社 | 混合冷媒 |
| US10330364B2 (en) | 2014-06-26 | 2019-06-25 | Hudson Technologies, Inc. | System and method for retrofitting a refrigeration system from HCFC to HFC refrigerant |
| ES2820350T3 (es) | 2014-09-25 | 2021-04-20 | Daikin Ind Ltd | Composición que comprende HFC y HFO |
| KR102504399B1 (ko) * | 2014-10-09 | 2023-03-02 | 에네오스 가부시키가이샤 | 냉동기유 및 냉동기용 작동 유체 조성물 |
| FR3033791B1 (fr) | 2015-03-18 | 2017-04-14 | Arkema France | Stabilisation du 1-chloro-3,3,3-trifluoropropene |
| CN104789192B (zh) * | 2015-04-17 | 2018-01-05 | 天津大学 | 适用于中低温冷冻冷藏系统的新型制冷剂 |
| CN105038711A (zh) * | 2015-07-30 | 2015-11-11 | 天津大学 | 一种含有1,1-二氟乙烷的混合制冷剂 |
| WO2017062642A1 (en) * | 2015-10-07 | 2017-04-13 | Honeywell Internationa Inc. | Methods and compositions for recharging systems and recharged systems |
| KR101898040B1 (ko) * | 2016-05-24 | 2018-09-12 | 김병열 | 온도센서를 이용한 캡슐형 소화장치 |
| CN105199674A (zh) * | 2015-10-30 | 2015-12-30 | 山东华安新材料有限公司 | 制冷剂组合物 |
| US10800958B2 (en) | 2015-11-20 | 2020-10-13 | Daikin Industries, Ltd. | Composition containing mixture of fluorinated hydrocarbons, and use thereof |
| JP6384563B2 (ja) * | 2016-03-31 | 2018-09-05 | ダイキン工業株式会社 | フッ素化炭化水素の混合物を含有する組成物及びその応用 |
| FR3057272B1 (fr) | 2016-10-10 | 2020-05-08 | Arkema France | Compositions azeotropiques a base de tetrafluoropropene |
| FR3057271B1 (fr) | 2016-10-10 | 2020-01-17 | Arkema France | Utilisation de compositions a base de tetrafluoropropene |
| EP3528893A1 (en) * | 2016-10-21 | 2019-08-28 | The Procter and Gamble Company | Concentrated shampoo comprising a hydrofluoroolefin or a hydrochlorofluoroolefin for delivering compositional and foam dosage property benefits |
| GB2565563B (en) * | 2017-08-16 | 2022-04-06 | Trio Gas Products Ltd | Heat transfer fluid |
| GB2557240A (en) * | 2016-12-01 | 2018-06-20 | Trio Gas Products Ltd | Heat transfer fluid |
| ES2908787T3 (es) * | 2017-01-13 | 2022-05-03 | Honeywell Int Inc | Refrigerante, composiciones de transferencia de calor, métodos y sistemas |
| FR3064275B1 (fr) * | 2017-03-21 | 2019-06-07 | Arkema France | Procede de chauffage et/ou climatisation d'un vehicule |
| FR3064264B1 (fr) | 2017-03-21 | 2019-04-05 | Arkema France | Composition a base de tetrafluoropropene |
| JP6504298B2 (ja) | 2017-04-21 | 2019-04-24 | ダイキン工業株式会社 | 冷媒を含有する組成物及びその応用 |
| JP6443576B2 (ja) | 2017-05-19 | 2018-12-26 | ダイキン工業株式会社 | 冷媒を含有する組成物、その使用、それを用いた冷凍方法、及びそれを含む冷凍機 |
| JP6418284B1 (ja) * | 2017-06-12 | 2018-11-07 | ダイキン工業株式会社 | 冷媒を含有する組成物、その使用、それを用いた冷凍方法、及びそれを含む冷凍機 |
| BR102017017568B1 (pt) * | 2017-08-16 | 2023-11-21 | Ideal Inteligência Energética Ltda | Composição de fluido refrigerante, uso da composição, produto envasado e processo de envasamento |
| WO2019038844A1 (ja) * | 2017-08-23 | 2019-02-28 | 三菱電機株式会社 | 蒸発器、冷凍サイクル装置およびユニットクーラ |
| JP6555315B2 (ja) * | 2017-10-16 | 2019-08-07 | ダイキン工業株式会社 | HFO−1234ze(E)及びHFC−134を含有する冷媒組成物及びその使用 |
| MX2020005612A (es) * | 2017-12-04 | 2020-09-24 | Chemours Co Fc Llc | Proceso e intermedios para preparar 1,1,3-tricloro-4,4,4-trifluoro but-1-eno y (e)-1,1,1,4,4,4-hexafluorobut-2-eno. |
| CN107987798B (zh) * | 2017-12-08 | 2021-01-29 | 西安近代化学研究所 | 一种环保混合制冷剂 |
| CN107987797B (zh) * | 2017-12-08 | 2021-01-29 | 西安近代化学研究所 | 一种替代hcfc-22的环保混合制冷剂 |
| CN112004908B (zh) * | 2018-04-25 | 2022-02-18 | 大金工业株式会社 | 含有制冷剂的组合物、其用途、利用其的冷冻方法和具有其的冷冻机 |
| JP7108212B2 (ja) | 2018-07-17 | 2022-07-28 | ダイキン工業株式会社 | 冷媒を含有する組成物、熱移動媒体及び熱サイクルシステム |
| KR102758475B1 (ko) | 2018-07-17 | 2025-01-22 | 다이킨 고교 가부시키가이샤 | 자동차용 냉동 사이클 장치 |
| CN114656934B (zh) | 2018-07-17 | 2024-07-05 | 大金工业株式会社 | 制冷剂循环装置 |
| JP2022502551A (ja) * | 2018-10-10 | 2022-01-11 | エスアールエフ リミテッド | 2,3,3,3−テトラフルオロプロペンを含む組成物 |
| WO2020152714A1 (en) * | 2019-01-24 | 2020-07-30 | Srf Limited | Compositions comprising 1,3,3,3-tetrafluoropropene |
| WO2020158257A1 (ja) | 2019-01-30 | 2020-08-06 | ダイキン工業株式会社 | 冷媒を含有する組成物、並びに、その組成物を用いた冷凍方法、冷凍装置の運転方法及び冷凍装置 |
| JP6844677B2 (ja) | 2019-01-30 | 2021-03-17 | ダイキン工業株式会社 | 冷媒を含有する組成物、並びに、その組成物を用いた冷凍方法、冷凍装置の運転方法及び冷凍装置 |
| WO2020162401A1 (ja) | 2019-02-05 | 2020-08-13 | ダイキン工業株式会社 | 冷媒を含有する組成物、並びに、その組成物を用いた冷凍方法、冷凍装置の運転方法及び冷凍装置 |
| CN113412398A (zh) | 2019-02-06 | 2021-09-17 | 大金工业株式会社 | 含有制冷剂的组合物及使用了该组合物的冷冻方法、冷冻装置的运转方法和冷冻装置 |
| JP2020139072A (ja) * | 2019-02-28 | 2020-09-03 | 出光興産株式会社 | 冷凍機用組成物 |
| CN113825821B (zh) * | 2019-04-29 | 2024-10-29 | 科慕埃弗西有限公司 | 溢流式系统中的制冷剂共混物 |
| CN110699042B (zh) * | 2019-09-30 | 2021-04-27 | 浙江衢化氟化学有限公司 | 一种氟代烯烃和氟代烷烃的组合物 |
| CN110964485B (zh) * | 2019-11-18 | 2021-02-05 | 珠海格力电器股份有限公司 | 一种混合制冷剂 |
| CN111040734A (zh) * | 2019-12-30 | 2020-04-21 | 山东华安新材料有限公司 | 一种HFC-152a的制冷剂组合物 |
| MX2022008896A (es) * | 2020-02-07 | 2022-08-15 | Chemours Co Fc Llc | Composiciones que comprenden 2,3,3,3-tetrafluoropropeno y metodos para elaborar y usar las composiciones. |
| JP2025531406A (ja) * | 2022-09-30 | 2025-09-19 | ハネウェル・インターナショナル・インコーポレーテッド | 冷媒、熱伝達組成物、並びに熱伝達システム及び方法 |
| WO2025048884A1 (en) * | 2023-08-31 | 2025-03-06 | The Chemours Company Fc, Llc | Tracer-containing compositions and methods of making and use thereof |
| CN117942524B (zh) * | 2024-01-19 | 2025-07-22 | 清华大学 | 一种电池灭火剂及其制备方法和应用 |
| WO2025174927A1 (en) * | 2024-02-16 | 2025-08-21 | The Chemours Company Fc, Llc | Purification of flourinated propenes by liquid phase adsorption |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19898C (de) | 1882-11-01 | W. R. ROWAN in Hamburg | Neuerungen an Dampfwagen für Eisenbahnen | |
| US5185094A (en) † | 1990-12-17 | 1993-02-09 | E. I. Du Pont De Nemours And Company | Constant boiling compositions of pentafluoroethane, difluoromethane, and tetrafluoroethane |
| GB9108527D0 (en) † | 1991-04-18 | 1991-06-05 | Ici Plc | Refrigerant compositions |
| US6606868B1 (en) † | 1999-10-04 | 2003-08-19 | Refrigerant Products, Ltd. | R 22 replacement refrigerant |
| US8444874B2 (en) † | 2002-10-25 | 2013-05-21 | Honeywell International Inc. | Heat transfer methods using heat transfer compositions containing trans-1,3,3,3-tetrafluoropropene |
| US7524805B2 (en) * | 2004-04-29 | 2009-04-28 | Honeywell International Inc. | Azeotrope-like compositions of tetrafluoropropene and hydrofluorocarbons |
| US20060243945A1 (en) * | 2005-03-04 | 2006-11-02 | Minor Barbara H | Compositions comprising a fluoroolefin |
| US7569170B2 (en) † | 2005-03-04 | 2009-08-04 | E.I. Du Pont De Nemours And Company | Compositions comprising a fluoroolefin |
| CN110003858A (zh) * | 2005-03-04 | 2019-07-12 | 科慕埃弗西有限公司 | 包含氟代烯烃的组合物 |
| US20060243944A1 (en) * | 2005-03-04 | 2006-11-02 | Minor Barbara H | Compositions comprising a fluoroolefin |
| TWI708756B (zh) * | 2005-06-24 | 2020-11-01 | 美商哈尼威爾國際公司 | 含有經氟取代之烯烴之組合物 |
| CN101827912A (zh) * | 2006-09-01 | 2010-09-08 | 纳幕尔杜邦公司 | 用于通过闭环循环使选定的热传递流体循环的方法 |
| EP2129644B1 (en) * | 2006-10-03 | 2020-07-01 | Mexichem Fluor S.A. de C.V. | Dehydrogenationhalogenation process for the production of c3-c6-(hydro)fluoroalkenes |
| JP5572284B2 (ja) * | 2007-02-27 | 2014-08-13 | Jx日鉱日石エネルギー株式会社 | 冷凍機油および冷凍機用作動流体組成物 |
| US8024937B2 (en) * | 2007-06-21 | 2011-09-27 | E. I. Du Pont De Nemours And Company | Method for leak detection in heat transfer systems |
| FR2932492B1 (fr) * | 2008-06-11 | 2010-07-30 | Arkema France | Compositions a base d'hydrofluoroolefines |
| FR2932494B1 (fr) * | 2008-06-11 | 2011-02-25 | Arkema France | Compositions a base d'hydrofluoroolefines |
| WO2010002022A1 (en) * | 2008-07-01 | 2010-01-07 | Daikin Industries, Ltd. | REFRIGERANT COMPOSITION COMPRISING PENTAFLUOROETHANE (HFC125), 2,3,3,3-TETRAFLUOROPROPENE (HFO1234yf) AND 1,1,1,2-TETRAFLUOROETHANE (HFC134a) |
| WO2010002023A1 (en) * | 2008-07-01 | 2010-01-07 | Daikin Industries, Ltd. | REFRIGERANT COMPOSITION COMPRISING DIFLUOROMETHANE (HFC32), 2,3,3,3-TETRAFLUOROPROPENE (HFO1234yf) AND 1,1,1,2-TETRAFLUOROETHANE (HFC134a) |
| US8026318B2 (en) * | 2008-08-22 | 2011-09-27 | Air Products And Chemicals, Inc. | Mixed polycycloaliphatic amines (MPCA) and MPCA alkylates |
| US11602908B1 (en) | 2021-08-23 | 2023-03-14 | Coretech System Co., Ltd. | Method of mesh generation for resin transfer molding process |
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| ES2556762T5 (es) | 2022-12-05 |
| AU2015200652B2 (en) | 2016-11-17 |
| AU2009316668A1 (en) | 2010-05-27 |
| KR101628421B1 (ko) | 2016-06-08 |
| BR122013002802A2 (pt) | 2016-01-05 |
| WO2010059677A3 (en) | 2010-07-15 |
| AU2017201000B2 (en) | 2018-11-08 |
| AU2009316668B2 (en) | 2014-12-04 |
| AU2015200652A1 (en) | 2015-03-05 |
| CN104726066A (zh) | 2015-06-24 |
| EP2367601A2 (en) | 2011-09-28 |
| DE202009019199U1 (de) | 2018-10-15 |
| JP5689068B2 (ja) | 2015-03-25 |
| CA2741871A1 (en) | 2011-05-27 |
| AU2017201000A1 (en) | 2017-03-09 |
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