MX2011003633A - Composiciones que comprenden 2,3,3,3-tetrafluoropropeno, 2-cloro-2,3,3,3-tetrafluoropropanol, acetato de 2-cloro-2,3,3,3-tetrafluoropropilo o (2-cloro-2,3,3,3-tetrafluorop ropoxil) cloruro de zinc. - Google Patents
Composiciones que comprenden 2,3,3,3-tetrafluoropropeno, 2-cloro-2,3,3,3-tetrafluoropropanol, acetato de 2-cloro-2,3,3,3-tetrafluoropropilo o (2-cloro-2,3,3,3-tetrafluorop ropoxil) cloruro de zinc.Info
- Publication number
- MX2011003633A MX2011003633A MX2011003633A MX2011003633A MX2011003633A MX 2011003633 A MX2011003633 A MX 2011003633A MX 2011003633 A MX2011003633 A MX 2011003633A MX 2011003633 A MX2011003633 A MX 2011003633A MX 2011003633 A MX2011003633 A MX 2011003633A
- Authority
- MX
- Mexico
- Prior art keywords
- chloro
- hfo
- acetate
- hcfc
- methyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 195
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 title claims abstract description 97
- ZGDAIZKZNKWBTM-UHFFFAOYSA-N 2-chloro-2,3,3,3-tetrafluoropropan-1-ol Chemical compound OCC(F)(Cl)C(F)(F)F ZGDAIZKZNKWBTM-UHFFFAOYSA-N 0.000 title claims abstract description 56
- JXLLSNNXICBZIS-UHFFFAOYSA-N (2-chloro-2,3,3,3-tetrafluoropropyl) acetate Chemical compound CC(=O)OCC(F)(Cl)C(F)(F)F JXLLSNNXICBZIS-UHFFFAOYSA-N 0.000 title claims abstract description 18
- YZNCFBREKILROT-UHFFFAOYSA-N (2-chloro-2,3,3,3-tetrafluoropropyl) hypochlorite;zinc Chemical compound [Zn].FC(F)(F)C(F)(Cl)COCl YZNCFBREKILROT-UHFFFAOYSA-N 0.000 title abstract 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims abstract description 157
- 150000001875 compounds Chemical class 0.000 claims abstract description 115
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims abstract description 113
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims abstract description 105
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 84
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 claims abstract description 80
- BAMUEXIPKSRTBS-UHFFFAOYSA-N 1,1-dichloro-1,2,2,2-tetrafluoroethane Chemical compound FC(F)(F)C(F)(Cl)Cl BAMUEXIPKSRTBS-UHFFFAOYSA-N 0.000 claims abstract description 73
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 72
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 60
- -1 CF3CHFCI) Chemical compound 0.000 claims abstract description 58
- BOUGCJDAQLKBQH-UHFFFAOYSA-N 1-chloro-1,2,2,2-tetrafluoroethane Chemical compound FC(Cl)C(F)(F)F BOUGCJDAQLKBQH-UHFFFAOYSA-N 0.000 claims abstract description 57
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims abstract description 56
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims abstract description 45
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims abstract description 45
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims abstract description 35
- 238000000034 method Methods 0.000 claims abstract description 30
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical compound FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 claims abstract description 28
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims abstract description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 24
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical compound FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims abstract description 21
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims abstract description 20
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 claims abstract description 18
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims abstract description 18
- MIZLGWKEZAPEFJ-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical compound FC=C(F)F MIZLGWKEZAPEFJ-UHFFFAOYSA-N 0.000 claims abstract description 17
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims abstract description 16
- 230000008569 process Effects 0.000 claims abstract description 15
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 claims abstract description 14
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims abstract description 13
- 238000004378 air conditioning Methods 0.000 claims abstract description 11
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims abstract description 10
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims abstract description 10
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims abstract description 9
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical compound CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 claims abstract description 9
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 238000005057 refrigeration Methods 0.000 claims abstract description 9
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims abstract description 8
- JQEQBVHLTKCNTI-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropyl acetate Chemical compound CC(=O)OCC(F)C(F)(F)F JQEQBVHLTKCNTI-UHFFFAOYSA-N 0.000 claims abstract description 8
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 claims abstract description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims abstract description 8
- MFOQKYXGXHZFDL-UHFFFAOYSA-N 3,4,4,4-tetrafluorobutan-2-one Chemical compound CC(=O)C(F)C(F)(F)F MFOQKYXGXHZFDL-UHFFFAOYSA-N 0.000 claims abstract description 5
- AOMUALOCHQKUCD-UHFFFAOYSA-N dodecyl 4-chloro-3-[[3-(4-methoxyphenyl)-3-oxopropanoyl]amino]benzoate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=C(Cl)C(NC(=O)CC(=O)C=2C=CC(OC)=CC=2)=C1 AOMUALOCHQKUCD-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 4
- HTHNTJCVPNKCPZ-UHFFFAOYSA-N 2-chloro-1,1-difluoroethene Chemical compound FC(F)=CCl HTHNTJCVPNKCPZ-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000002904 solvent Substances 0.000 claims description 89
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 21
- KEGQZXLRQSXPJU-UHFFFAOYSA-N 1,3-difluoro-1,3-bis(trifluoromethyl)cyclobutane Chemical compound FC(F)(F)C1(F)CC(F)(C(F)(F)F)C1 KEGQZXLRQSXPJU-UHFFFAOYSA-N 0.000 claims description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 13
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- UENGBOCGGKLVJJ-UHFFFAOYSA-N 2-chloro-1-(2,4-difluorophenyl)ethanone Chemical compound FC1=CC=C(C(=O)CCl)C(F)=C1 UENGBOCGGKLVJJ-UHFFFAOYSA-N 0.000 claims description 9
- GIUIQFXYGQJOIZ-UHFFFAOYSA-M [Cl-].[Zn++].[O-]CC(F)(Cl)C(F)(F)F Chemical compound [Cl-].[Zn++].[O-]CC(F)(Cl)C(F)(F)F GIUIQFXYGQJOIZ-UHFFFAOYSA-M 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- JVTSHOJDBRTPHD-UHFFFAOYSA-N 2,2,2-trifluoroacetaldehyde Chemical compound FC(F)(F)C=O JVTSHOJDBRTPHD-UHFFFAOYSA-N 0.000 claims description 6
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 5
- 125000005270 trialkylamine group Chemical group 0.000 claims description 5
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 4
- XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 claims description 4
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 claims description 4
- MRQDALCRZBHBEM-UHFFFAOYSA-N 3-chloro-3,4,4,4-tetrafluorobutan-2-one Chemical compound CC(=O)C(F)(Cl)C(F)(F)F MRQDALCRZBHBEM-UHFFFAOYSA-N 0.000 claims description 3
- RQMWVVBHJMUJNZ-UHFFFAOYSA-N 4-chloropyridin-2-amine Chemical group NC1=CC(Cl)=CC=N1 RQMWVVBHJMUJNZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000005265 dialkylamine group Chemical group 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- ILAUSMKPJVMSSC-UHFFFAOYSA-N (2-chloro-2,3,3,3-tetrafluoropropyl) formate Chemical compound FC(F)(F)C(F)(Cl)COC=O ILAUSMKPJVMSSC-UHFFFAOYSA-N 0.000 claims description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 2
- RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 claims 8
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 claims 2
- WFLOTYSKFUPZQB-OWOJBTEDSA-N (e)-1,2-difluoroethene Chemical compound F\C=C\F WFLOTYSKFUPZQB-OWOJBTEDSA-N 0.000 claims 1
- 241000132092 Aster Species 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- DASQIKOOFDJYKA-UHFFFAOYSA-N CCIF Chemical compound CCIF DASQIKOOFDJYKA-UHFFFAOYSA-N 0.000 abstract 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 70
- 229910052751 metal Inorganic materials 0.000 description 38
- 239000002184 metal Substances 0.000 description 38
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 37
- 239000011541 reaction mixture Substances 0.000 description 35
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 23
- 239000007791 liquid phase Substances 0.000 description 23
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- 150000001299 aldehydes Chemical class 0.000 description 18
- 239000007789 gas Substances 0.000 description 18
- 229930040373 Paraformaldehyde Natural products 0.000 description 17
- 239000000047 product Substances 0.000 description 17
- CDOOAUSHHFGWSA-OWOJBTEDSA-N (e)-1,3,3,3-tetrafluoroprop-1-ene Chemical compound F\C=C\C(F)(F)F CDOOAUSHHFGWSA-OWOJBTEDSA-N 0.000 description 16
- 239000012535 impurity Substances 0.000 description 16
- 229920002866 paraformaldehyde Polymers 0.000 description 16
- 239000011701 zinc Substances 0.000 description 16
- 239000000243 solution Substances 0.000 description 14
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 14
- 229910052725 zinc Inorganic materials 0.000 description 13
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 12
- 238000004458 analytical method Methods 0.000 description 11
- 239000007795 chemical reaction product Substances 0.000 description 11
- 239000012071 phase Substances 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 10
- 239000007810 chemical reaction solvent Substances 0.000 description 10
- 238000003786 synthesis reaction Methods 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- 230000032050 esterification Effects 0.000 description 8
- 238000005886 esterification reaction Methods 0.000 description 8
- 230000010354 integration Effects 0.000 description 8
- 239000012808 vapor phase Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 239000011592 zinc chloride Substances 0.000 description 7
- 235000005074 zinc chloride Nutrition 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 238000005906 dihydroxylation reaction Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229910052749 magnesium Inorganic materials 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- 150000003222 pyridines Chemical group 0.000 description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 239000004246 zinc acetate Substances 0.000 description 5
- XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 239000012024 dehydrating agents Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000012299 nitrogen atmosphere Substances 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- 238000010926 purge Methods 0.000 description 4
- 150000003751 zinc Chemical class 0.000 description 4
- DPPHNCGGFCAZGX-UHFFFAOYSA-N 1,1-difluorocyclobutane Chemical compound FC1(F)CCC1 DPPHNCGGFCAZGX-UHFFFAOYSA-N 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 3
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 239000001273 butane Substances 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000012046 mixed solvent Substances 0.000 description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 239000003345 natural gas Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 238000010792 warming Methods 0.000 description 3
- FDOPVENYMZRARC-UHFFFAOYSA-N 1,1,1,2,2-pentafluoropropane Chemical compound CC(F)(F)C(F)(F)F FDOPVENYMZRARC-UHFFFAOYSA-N 0.000 description 2
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 2
- CAQPTDOAJUMIAI-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropan-1-ol Chemical compound OCC(F)C(F)(F)F CAQPTDOAJUMIAI-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 239000012459 cleaning agent Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 238000005796 dehydrofluorination reaction Methods 0.000 description 2
- 239000002274 desiccant Substances 0.000 description 2
- 239000003989 dielectric material Substances 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 239000008246 gaseous mixture Substances 0.000 description 2
- 229910000856 hastalloy Inorganic materials 0.000 description 2
- 229910052738 indium Inorganic materials 0.000 description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000003507 refrigerant Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 150000003462 sulfoxides Chemical group 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- VNDYJBBGRKZCSX-UHFFFAOYSA-L zinc bromide Chemical compound Br[Zn]Br VNDYJBBGRKZCSX-UHFFFAOYSA-L 0.000 description 2
- DFCMCMCPQIFPFT-UHFFFAOYSA-N (2-chloro-2,3,3,3-tetrafluoropropyl) hypochlorite Chemical group FC(F)(F)C(F)(Cl)COCl DFCMCMCPQIFPFT-UHFFFAOYSA-N 0.000 description 1
- ZDCWZRQSHBQRGN-UHFFFAOYSA-N 1,1,1,2,3-pentafluoropropane Chemical compound FCC(F)C(F)(F)F ZDCWZRQSHBQRGN-UHFFFAOYSA-N 0.000 description 1
- JPSKCQCQZUGWNM-UHFFFAOYSA-N 2,7-Oxepanedione Chemical compound O=C1CCCCC(=O)O1 JPSKCQCQZUGWNM-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- AJKVQEKCUACUMD-UHFFFAOYSA-N 2-Acetylpyridine Chemical compound CC(=O)C1=CC=CC=N1 AJKVQEKCUACUMD-UHFFFAOYSA-N 0.000 description 1
- RQBSYMINZKITIR-UHFFFAOYSA-N 2-chloro-3,3,3-trifluoropropan-1-ol Chemical compound OCC(Cl)C(F)(F)F RQBSYMINZKITIR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- ZKPUPHSBFMNFHO-UHFFFAOYSA-N [ClH]1C=CC=C1 Chemical compound [ClH]1C=CC=C1 ZKPUPHSBFMNFHO-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- WFKAJVHLWXSISD-UHFFFAOYSA-N anhydrous dimethyl-acetamide Natural products CC(C)C(N)=O WFKAJVHLWXSISD-UHFFFAOYSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- YHASWHZGWUONAO-UHFFFAOYSA-N butanoyl butanoate Chemical compound CCCC(=O)OC(=O)CCC YHASWHZGWUONAO-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000012777 commercial manufacturing Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- QUQFTIVBFKLPCL-UHFFFAOYSA-L copper;2-amino-3-[(2-amino-2-carboxylatoethyl)disulfanyl]propanoate Chemical compound [Cu+2].[O-]C(=O)C(N)CSSCC(N)C([O-])=O QUQFTIVBFKLPCL-UHFFFAOYSA-L 0.000 description 1
- 150000001930 cyclobutanes Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- QHNXEVRKFKHMRL-UHFFFAOYSA-N dimethylazanium;acetate Chemical compound CNC.CC(O)=O QHNXEVRKFKHMRL-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical compound O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- WGIWBXUNRXCYRA-UHFFFAOYSA-H trizinc;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O WGIWBXUNRXCYRA-UHFFFAOYSA-H 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
- 229960000314 zinc acetate Drugs 0.000 description 1
- 229940102001 zinc bromide Drugs 0.000 description 1
- 229960001939 zinc chloride Drugs 0.000 description 1
- 239000011746 zinc citrate Substances 0.000 description 1
- 235000006076 zinc citrate Nutrition 0.000 description 1
- 229940068475 zinc citrate Drugs 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
-
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C21/00—Acyclic unsaturated compounds containing halogen atoms
- C07C21/02—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds
- C07C21/18—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds containing fluorine
-
- 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
- C09K3/14—Anti-slip materials; Abrasives
-
- 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
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/10—Components
- C09K2205/12—Hydrocarbons
- C09K2205/126—Unsaturated fluorinated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Dispersion Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10433408P | 2008-10-10 | 2008-10-10 | |
| PCT/US2009/060094 WO2010042781A2 (en) | 2008-10-10 | 2009-10-09 | Compositions comprising 2,3,3,3-tetrafluoropropene, 2-chloro-2,3,3,3-tetrafluoropropanol, 2-chloro-2,3,3,3-tetrafluoro-propyl acetate or zinc (2-chloro-2,3,3,3-tetrafluoropropoxy) chloride |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2011003633A true MX2011003633A (es) | 2011-05-02 |
Family
ID=41571037
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2011003633A MX2011003633A (es) | 2008-10-10 | 2009-10-09 | Composiciones que comprenden 2,3,3,3-tetrafluoropropeno, 2-cloro-2,3,3,3-tetrafluoropropanol, acetato de 2-cloro-2,3,3,3-tetrafluoropropilo o (2-cloro-2,3,3,3-tetrafluorop ropoxil) cloruro de zinc. |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US8147710B2 (OSRAM) |
| EP (1) | EP2331489A2 (OSRAM) |
| JP (1) | JP2012505296A (OSRAM) |
| KR (1) | KR20110084910A (OSRAM) |
| CN (1) | CN102177118A (OSRAM) |
| AU (1) | AU2009302263A1 (OSRAM) |
| BR (1) | BRPI0913806A2 (OSRAM) |
| CA (1) | CA2736216A1 (OSRAM) |
| MX (1) | MX2011003633A (OSRAM) |
| RU (1) | RU2011118429A (OSRAM) |
| TW (1) | TW201022425A (OSRAM) |
| WO (1) | WO2010042781A2 (OSRAM) |
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG10201707158QA (en) * | 2008-05-07 | 2017-10-30 | Du Pont | Compositions comprising 1,1,1,2,3-pentafluoropropane or 2,3,3,3- tetrafluoropropene |
| HRP20220650T1 (hr) | 2008-05-07 | 2022-07-08 | The Chemours Company Fc, Llc | Pripravci |
| WO2010042781A2 (en) | 2008-10-10 | 2010-04-15 | E. I. Du Pont De Nemours And Company | Compositions comprising 2,3,3,3-tetrafluoropropene, 2-chloro-2,3,3,3-tetrafluoropropanol, 2-chloro-2,3,3,3-tetrafluoro-propyl acetate or zinc (2-chloro-2,3,3,3-tetrafluoropropoxy) chloride |
| CN103025844B (zh) | 2010-08-13 | 2019-05-03 | 开利公司 | 氟化烃组合物 |
| IT1406472B1 (it) | 2010-12-22 | 2014-02-28 | Nuovo Pignone Spa | Prova per similitudine di prestazione di compressore |
| WO2012157764A1 (ja) * | 2011-05-19 | 2012-11-22 | 旭硝子株式会社 | 作動媒体および熱サイクルシステム |
| US8845922B2 (en) * | 2011-12-20 | 2014-09-30 | Honeywell International Inc. | Compositions and use of vinylidene fluoride and blends thereof |
| CN102766022A (zh) * | 2012-08-09 | 2012-11-07 | 西安近代化学研究所 | 3，3，3-三氟丙醇的合成方法 |
| US9321867B2 (en) | 2012-12-21 | 2016-04-26 | Honeywell International Inc. | Synthesis of 2,3,3,3-tetrafluoropropene/vinylidene fluoride copolymers |
| FR3000096B1 (fr) * | 2012-12-26 | 2015-02-20 | Arkema France | Composition comprenant du 2,3,3,3-tetrafluoropropene |
| CN104968757A (zh) * | 2013-02-05 | 2015-10-07 | 旭硝子株式会社 | 热泵用工作介质以及热泵系统 |
| CN105392859B (zh) * | 2013-03-14 | 2018-05-04 | 霍尼韦尔国际公司 | 包含偏二氟乙烯的组合物和方法 |
| JP6038287B2 (ja) * | 2013-03-28 | 2016-12-07 | 三菱電機株式会社 | スクロール圧縮機及びそれを備えた冷凍サイクル装置 |
| CN105164228B (zh) * | 2013-04-30 | 2019-06-11 | Ａｇｃ株式会社 | 热循环用工作介质 |
| JP6379391B2 (ja) * | 2013-04-30 | 2018-08-29 | Ａｇｃ株式会社 | トリフルオロエチレンを含む組成物 |
| JP5850204B2 (ja) * | 2013-07-12 | 2016-02-03 | 旭硝子株式会社 | 熱サイクル用作動媒体、熱サイクルシステム用組成物および熱サイクルシステム |
| GB2535383B (en) | 2013-07-30 | 2016-10-19 | Mexichem Amanco Holding Sa | Heat transfer compositions |
| DE112015000583T5 (de) | 2014-01-31 | 2016-11-03 | Asahi Glass Company, Limited | Arbeitsfluid für einen Wärmekreisprozess, Zusammensetzung für ein Wärmekreisprozesssystem und Wärmekreisprozesssystem |
| EP4417667A1 (en) * | 2014-01-31 | 2024-08-21 | Agc Inc. | Working fluid for heat cycle, composition for heat cycle system, and heat cycle system |
| WO2015115551A1 (ja) * | 2014-01-31 | 2015-08-06 | 旭硝子株式会社 | 作動媒体の製造方法 |
| WO2015125876A1 (ja) * | 2014-02-20 | 2015-08-27 | 旭硝子株式会社 | 熱サイクルシステム用組成物および熱サイクルシステム |
| MY178665A (en) * | 2014-02-20 | 2020-10-20 | Asahi Glass Co Ltd | Composition for heat cycle system, and heat cycle system |
| EP3109292B1 (en) | 2014-02-20 | 2020-09-02 | AGC Inc. | Working fluid for heat cycle |
| WO2015125884A1 (ja) | 2014-02-20 | 2015-08-27 | 旭硝子株式会社 | 熱サイクルシステム用組成物および熱サイクルシステム |
| EP3812446B1 (en) | 2014-02-20 | 2023-06-28 | Agc Inc. | Composition for heat cycle system, and heat cycle system |
| WO2015125880A1 (ja) * | 2014-02-20 | 2015-08-27 | 旭硝子株式会社 | 熱サイクルシステム用組成物および熱サイクルシステム |
| JP6540685B2 (ja) * | 2014-02-28 | 2019-07-10 | Ａｇｃ株式会社 | 熱サイクル用作動媒体、熱サイクルシステム用組成物および熱サイクルシステム |
| WO2015133587A1 (ja) * | 2014-03-06 | 2015-09-11 | 旭硝子株式会社 | 熱サイクル用作動媒体および熱サイクルシステム |
| WO2015132963A1 (ja) * | 2014-03-07 | 2015-09-11 | 三菱電機株式会社 | 熱交換器及び空気調和機 |
| WO2015136704A1 (ja) * | 2014-03-14 | 2015-09-17 | 三菱電機株式会社 | 圧縮機及び冷凍サイクル装置 |
| CN105899889B (zh) * | 2014-03-14 | 2018-06-26 | 三菱电机株式会社 | 制冷装置 |
| WO2015136980A1 (ja) * | 2014-03-14 | 2015-09-17 | 三菱電機株式会社 | 冷凍サイクル装置 |
| WO2015140884A1 (ja) * | 2014-03-17 | 2015-09-24 | 三菱電機株式会社 | 冷凍サイクル装置 |
| CN205955984U (zh) * | 2014-03-17 | 2017-02-15 | 三菱电机株式会社 | 涡旋压缩机 |
| EP3128259A1 (en) * | 2014-03-17 | 2017-02-08 | Mitsubishi Electric Corporation | Heat pump device |
| CN106104171A (zh) * | 2014-03-17 | 2016-11-09 | 三菱电机株式会社 | 蓄积器以及制冷循环装置 |
| EP3121243A4 (en) | 2014-03-17 | 2017-11-08 | Asahi Glass Company, Limited | Working medium for heat cycles, composition for heat-cycle systems, and heat-cycle system |
| EP3121538A1 (en) * | 2014-03-17 | 2017-01-25 | Mitsubishi Electric Corporation | Refrigeration cycle apparatus |
| EP3121242B1 (en) * | 2014-03-18 | 2019-05-08 | AGC Inc. | Working fluid for heat cycle, composition for heat-cycle systems, and heat-cycle system |
| CN106133109B (zh) | 2014-03-18 | 2021-05-04 | Ａｇｃ株式会社 | 热循环系统用组合物以及热循环系统 |
| EP3241879B1 (en) | 2014-09-25 | 2020-07-01 | Daikin Industries, Ltd. | Composition comprising hfc and hfo |
| AU2014408863B2 (en) * | 2014-10-16 | 2019-01-03 | Mitsubishi Electric Corporation | Refrigeration cycle apparatus |
| EP3208555A4 (en) * | 2014-10-16 | 2018-05-30 | Mitsubishi Electric Corporation | Refrigeration cycle device |
| GB201501598D0 (en) | 2015-01-30 | 2015-03-18 | Mexichem Fluor Sa De Cv | Compositions |
| PL3141587T3 (pl) | 2015-02-19 | 2019-11-29 | Daikin Ind Ltd | Kompozycja zawierająca mieszaninę fluorowanych węglowodorów i sposób jej wytwarzania |
| WO2016181910A1 (ja) * | 2015-05-12 | 2016-11-17 | 旭硝子株式会社 | 熱サイクルシステム用組成物および熱サイクルシステム |
| JP6848861B2 (ja) * | 2015-06-01 | 2021-03-24 | Ａｇｃ株式会社 | 熱サイクル用作動媒体、熱サイクルシステム用組成物および熱サイクルシステム |
| JP2018123691A (ja) | 2017-01-30 | 2018-08-09 | ダイキン工業株式会社 | 圧縮機 |
| GB2582364A (en) * | 2019-03-21 | 2020-09-23 | Mexichem Fluor Sa De Cv | Methods |
| US20220112226A1 (en) * | 2020-10-14 | 2022-04-14 | Honeywell International Inc. | Trifluoroacetyl iodide compositions useful for making trifluoroiodomethane |
| CN116694305B (zh) * | 2022-02-28 | 2025-09-16 | 山东东岳未来氢能材料股份有限公司 | 含三氟乙酰氟的低gwp值组合物及其用途 |
| CN116098816A (zh) * | 2022-07-21 | 2023-05-12 | 北京市春立正达医疗器械股份有限公司 | 一种氟化防龋泡沫的制作方法 |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2970988A (en) * | 1955-10-14 | 1961-02-07 | Minnesota Mining & Mfg | New fluorine-containing polymers and preparation thereof |
| GB1122847A (en) * | 1966-02-07 | 1968-08-07 | Ici Ltd | Fluorine-containing organic compounds |
| GB8415201D0 (en) * | 1984-06-14 | 1984-07-18 | Ici Plc | Chemical process |
| US5595661A (en) * | 1994-08-03 | 1997-01-21 | Schering Corporation | Process for recover halocarbons from liquid waste slurries |
| GB0107705D0 (en) * | 2001-03-28 | 2001-05-16 | Ineos Fluor Ltd | Purification of saturated halocarbons |
| US7279451B2 (en) * | 2002-10-25 | 2007-10-09 | Honeywell International Inc. | Compositions containing fluorine substituted olefins |
| US20090253820A1 (en) * | 2006-03-21 | 2009-10-08 | Honeywell International Inc. | Foaming agents and compositions containing fluorine sustituted olefins and methods of foaming |
| US20050211949A1 (en) * | 2003-11-13 | 2005-09-29 | Bivens Donald B | Detectable refrigerant compositions and uses thereof |
| US7641809B2 (en) * | 2004-02-26 | 2010-01-05 | E. I. Du Pont De Nemours And Company | Tracer-containing compositions |
| CN1954209A (zh) * | 2004-03-17 | 2007-04-25 | 索尔维公司 | 分析1,1,1,2－四氟乙烷的方法 |
| US7951982B2 (en) | 2004-04-29 | 2011-05-31 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| TW200634141A (en) * | 2004-12-21 | 2006-10-01 | Honeywell Int Inc | Stabilized iodocarbon compositions |
| US20060243945A1 (en) | 2005-03-04 | 2006-11-02 | Minor Barbara H | Compositions comprising a fluoroolefin |
| US20060243944A1 (en) * | 2005-03-04 | 2006-11-02 | Minor Barbara H | Compositions comprising a fluoroolefin |
| US7396965B2 (en) | 2005-05-12 | 2008-07-08 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| WO2008002499A2 (en) * | 2006-06-27 | 2008-01-03 | E. I. Du Pont De Nemours And Company | Tetrafluoropropene production processes |
| ES2447037T3 (es) | 2006-09-05 | 2014-03-11 | E.I. Du Pont De Nemours And Company | Procedimiento de fabricación de 2,3,3,3-tetrafluoropropeno |
| ES2543348T3 (es) | 2006-09-05 | 2015-08-18 | E.I. Du Pont De Nemours And Company | Procedimiento de deshidrofluoración para fabricar hidrofluoroolefinas |
| US7981312B2 (en) * | 2006-10-31 | 2011-07-19 | E. I. Du Pont De Nemours And Company | Processes for producing and compositions comprising 2,3,3,3-tetrafluoropropene and/or 1,2,3,3-tetrafluoropropene |
| WO2008053811A1 (en) * | 2006-11-01 | 2008-05-08 | Daikin Industries, Ltd. | Method for producing olefin |
| GB0625214D0 (en) * | 2006-12-19 | 2007-01-24 | Ineos Fluor Holdings Ltd | Process |
| CN103396506A (zh) * | 2006-12-20 | 2013-11-20 | 霍尼韦尔国际公司 | 用于阻透的共聚物 |
| BRPI0818958A2 (pt) * | 2007-11-20 | 2017-12-12 | Du Pont | "processos para a fabricação dos hidrofluoroalquenos, para a fabricação dos hidrofluoroalcanóis, para a fabricação dos hidrofluoroésteres e composto" |
| US8058488B2 (en) | 2007-11-20 | 2011-11-15 | E. I. Du Pont De Nemours And Company | Synthesis of hydrofluoroalkanols and hydrofluoroalkenes |
| HRP20220650T1 (hr) * | 2008-05-07 | 2022-07-08 | The Chemours Company Fc, Llc | Pripravci |
| SG10201707158QA (en) * | 2008-05-07 | 2017-10-30 | Du Pont | Compositions comprising 1,1,1,2,3-pentafluoropropane or 2,3,3,3- tetrafluoropropene |
| US20090325445A1 (en) * | 2008-06-27 | 2009-12-31 | Bogdan Mary C | Method of insulating temporary polymeric structures with polyurethane or polyisocyanurate foam |
| WO2010042781A2 (en) * | 2008-10-10 | 2010-04-15 | E. I. Du Pont De Nemours And Company | Compositions comprising 2,3,3,3-tetrafluoropropene, 2-chloro-2,3,3,3-tetrafluoropropanol, 2-chloro-2,3,3,3-tetrafluoro-propyl acetate or zinc (2-chloro-2,3,3,3-tetrafluoropropoxy) chloride |
| US20100172701A1 (en) * | 2008-12-12 | 2010-07-08 | Honeywell International Inc. | Barrier fortification enhancement and building structural units |
-
2009
- 2009-10-09 WO PCT/US2009/060094 patent/WO2010042781A2/en not_active Ceased
- 2009-10-09 JP JP2011531192A patent/JP2012505296A/ja active Pending
- 2009-10-09 RU RU2011118429/04A patent/RU2011118429A/ru not_active Application Discontinuation
- 2009-10-09 CN CN2009801401143A patent/CN102177118A/zh active Pending
- 2009-10-09 AU AU2009302263A patent/AU2009302263A1/en not_active Abandoned
- 2009-10-09 CA CA2736216A patent/CA2736216A1/en not_active Abandoned
- 2009-10-09 TW TW098134421A patent/TW201022425A/zh unknown
- 2009-10-09 EP EP09748568A patent/EP2331489A2/en not_active Withdrawn
- 2009-10-09 KR KR1020117010557A patent/KR20110084910A/ko not_active Withdrawn
- 2009-10-09 BR BRPI0913806A patent/BRPI0913806A2/pt not_active IP Right Cessation
- 2009-10-09 MX MX2011003633A patent/MX2011003633A/es active IP Right Grant
- 2009-10-09 US US12/576,388 patent/US8147710B2/en not_active Expired - Fee Related
-
2012
- 2012-02-27 US US13/405,657 patent/US8518294B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US8518294B2 (en) | 2013-08-27 |
| US8147710B2 (en) | 2012-04-03 |
| AU2009302263A1 (en) | 2010-04-15 |
| CN102177118A (zh) | 2011-09-07 |
| BRPI0913806A2 (pt) | 2015-10-20 |
| CA2736216A1 (en) | 2010-04-15 |
| KR20110084910A (ko) | 2011-07-26 |
| WO2010042781A3 (en) | 2010-07-08 |
| EP2331489A2 (en) | 2011-06-15 |
| US20120168672A1 (en) | 2012-07-05 |
| TW201022425A (en) | 2010-06-16 |
| JP2012505296A (ja) | 2012-03-01 |
| US20100090156A1 (en) | 2010-04-15 |
| WO2010042781A2 (en) | 2010-04-15 |
| RU2011118429A (ru) | 2012-11-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX2011003633A (es) | Composiciones que comprenden 2,3,3,3-tetrafluoropropeno, 2-cloro-2,3,3,3-tetrafluoropropanol, acetato de 2-cloro-2,3,3,3-tetrafluoropropilo o (2-cloro-2,3,3,3-tetrafluorop ropoxil) cloruro de zinc. | |
| JP7254123B2 (ja) | ２，３，３，３－テトラフルオロプロペン、１，１，２，３－テトラクロロプロペン、２－クロロ－３，３，３－トリフルオロプロペン、または２－クロロ－１，１，１，２－テトラフルオロプロパンを含む組成物 | |
| AU2023202867B2 (en) | 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 | |
| US8058488B2 (en) | Synthesis of hydrofluoroalkanols and hydrofluoroalkenes | |
| CN101861322B (zh) | 氢氟链烷醇和氢氟烯烃的合成 | |
| HK1162018A (en) | Compositions comprising 2,3,3,3-tetrafluoropropene, 2-chloro-2,3,3,3-tetrafluoropropanol, 2-chloro-2,3,3,3-tetrafluoro-propyl acetate or zinc (2-chloro-2,3,3,3-tetrafluoropropoxy) chloride | |
| WO2018165608A1 (en) | Processes for preparing partially fluorinated epoxides and perfluorinated epoxides and compositions related thereto | |
| HK1149271A (en) | Synthesis of hydrofluoroalkanols and hydrofluoroalkenes |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |