CN103842075A - 1,1,2-三氯乙烷和/或1,2-二氯乙烯催化气相氟化制备1-氯-2,2-二氟乙烷 - Google Patents
1,1,2-三氯乙烷和/或1,2-二氯乙烯催化气相氟化制备1-氯-2,2-二氟乙烷 Download PDFInfo
- Publication number
- CN103842075A CN103842075A CN201280049801.6A CN201280049801A CN103842075A CN 103842075 A CN103842075 A CN 103842075A CN 201280049801 A CN201280049801 A CN 201280049801A CN 103842075 A CN103842075 A CN 103842075A
- Authority
- CN
- China
- Prior art keywords
- catalyst
- difluoroethane
- chloro
- dichloroethene
- trichloroethanes
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- UBOXGVDOUJQMTN-UHFFFAOYSA-N 1,1,2-trichloroethane Chemical compound ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 title claims abstract description 20
- KFUSEUYYWQURPO-UHFFFAOYSA-N 1,2-dichloroethene Chemical compound ClC=CCl KFUSEUYYWQURPO-UHFFFAOYSA-N 0.000 title claims abstract description 13
- 238000003682 fluorination reaction Methods 0.000 title claims abstract description 12
- ATEBGNALLCMSGS-UHFFFAOYSA-N 2-chloro-1,1-difluoroethane Chemical compound FC(F)CCl ATEBGNALLCMSGS-UHFFFAOYSA-N 0.000 title abstract description 6
- 230000003197 catalytic effect Effects 0.000 title abstract 2
- 239000003054 catalyst Substances 0.000 claims abstract description 85
- 238000000034 method Methods 0.000 claims abstract description 30
- 238000002360 preparation method Methods 0.000 claims abstract description 15
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 8
- 238000006243 chemical reaction Methods 0.000 claims description 28
- 239000011651 chromium Substances 0.000 claims description 15
- 239000012190 activator Substances 0.000 claims description 7
- 239000004411 aluminium Substances 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- IHNDUGMUECOVKK-UHFFFAOYSA-N aluminum chromium(3+) oxygen(2-) Chemical compound [O-2].[Cr+3].[O-2].[Al+3] IHNDUGMUECOVKK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- 230000008569 process Effects 0.000 abstract description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 abstract 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 2
- PHFQLYPOURZARY-UHFFFAOYSA-N chromium trinitrate Chemical compound [Cr+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PHFQLYPOURZARY-UHFFFAOYSA-N 0.000 abstract 2
- 238000000151 deposition Methods 0.000 abstract 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 abstract 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 abstract 1
- 229910001629 magnesium chloride Inorganic materials 0.000 abstract 1
- KBJMLQFLOWQJNF-UHFFFAOYSA-N nickel(II) nitrate Inorganic materials [Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O KBJMLQFLOWQJNF-UHFFFAOYSA-N 0.000 abstract 1
- 239000011592 zinc chloride Substances 0.000 abstract 1
- 235000005074 zinc chloride Nutrition 0.000 abstract 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 42
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- 239000007789 gas Substances 0.000 description 15
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 7
- 239000012071 phase Substances 0.000 description 6
- 230000004913 activation Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- WGLPBDUCMAPZCE-UHFFFAOYSA-N chromium trioxide Inorganic materials O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 4
- 150000004673 fluoride salts Chemical class 0.000 description 4
- 239000011261 inert gas Substances 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
- 238000002441 X-ray diffraction Methods 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 229940117975 chromium trioxide Drugs 0.000 description 3
- GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000004441 surface measurement Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- RHBRWKIPYGZNMP-UHFFFAOYSA-N [O--].[O--].[O--].[Al+3].[Cr+3] Chemical compound [O--].[O--].[O--].[Al+3].[Cr+3] RHBRWKIPYGZNMP-UHFFFAOYSA-N 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 229910001026 inconel Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- UKDOTCFNLHHKOF-FGRDZWBJSA-N (z)-1-chloroprop-1-ene;(z)-1,2-dichloroethene Chemical group C\C=C/Cl.Cl\C=C/Cl UKDOTCFNLHHKOF-FGRDZWBJSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical class CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- JHJOAXHWIIFJJU-UHFFFAOYSA-N 1,2-difluoroethane Chemical compound F[CH]CF JHJOAXHWIIFJJU-UHFFFAOYSA-N 0.000 description 1
- VEZJSKSPVQQGIS-UHFFFAOYSA-N 1-chloro-2-fluoroethane Chemical class FCCCl VEZJSKSPVQQGIS-UHFFFAOYSA-N 0.000 description 1
- 229910016569 AlF 3 Inorganic materials 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- YQKXQANMUVRKDF-UHFFFAOYSA-K O.[F-].[F-].[F-].F.F.[Al+3] Chemical compound O.[F-].[F-].[F-].F.F.[Al+3] YQKXQANMUVRKDF-UHFFFAOYSA-K 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical group [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- -1 chromium oxide (Cr 2o 3) fluoride salt Chemical class 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000006253 efflorescence Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010574 gas phase reaction Methods 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/22—Halogenating
- B01J37/26—Fluorinating
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/06—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of zinc, cadmium or mercury
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/86—Chromium
- B01J23/862—Iron and chromium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/86—Chromium
- B01J23/866—Nickel and chromium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/138—Halogens; Compounds thereof with alkaline earth metals, magnesium, beryllium, zinc, cadmium or mercury
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C07C17/202—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
- C07C17/206—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction the other compound being HX
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C07C17/21—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms with simultaneous increase of the number of halogen atoms
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/18—Carbon
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
Description
Claims (10)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2938DE2011 | 2011-10-12 | ||
IN2938/2011 | 2011-10-12 | ||
PCT/EP2012/070126 WO2013053800A2 (en) | 2011-10-12 | 2012-10-11 | Catalytic gas phase fluorination of 1,1,2-trichloroethane and/or 1,2-dichloroethene to produce 1-chloro-2,2-difluoroethane |
Publications (2)
Publication Number | Publication Date |
---|---|
CN103842075A true CN103842075A (zh) | 2014-06-04 |
CN103842075B CN103842075B (zh) | 2016-08-17 |
Family
ID=48082605
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201280049801.6A Active CN103842075B (zh) | 2011-10-12 | 2012-10-11 | 1,1,2-三氯乙烷和/或1,2-二氯乙烯催化气相氟化制备1-氯-2,2-二氟乙烷 |
Country Status (13)
Country | Link |
---|---|
US (1) | US9000242B2 (zh) |
EP (1) | EP2766117B1 (zh) |
JP (1) | JP6078073B2 (zh) |
KR (1) | KR101999136B1 (zh) |
CN (1) | CN103842075B (zh) |
BR (1) | BR112014008902B1 (zh) |
DK (1) | DK2766117T3 (zh) |
ES (1) | ES2674149T3 (zh) |
IL (1) | IL231760A (zh) |
IN (1) | IN2014CN02632A (zh) |
MX (1) | MX340808B (zh) |
TW (1) | TWI615194B (zh) |
WO (1) | WO2013053800A2 (zh) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104692997A (zh) * | 2015-02-11 | 2015-06-10 | 巨化集团技术中心 | 一种1,1-二氟-2-氯乙烷的制备方法 |
CN104692998A (zh) * | 2015-02-11 | 2015-06-10 | 巨化集团技术中心 | 1,1-二氟-2-氯乙烷的制备方法 |
CN107001196A (zh) * | 2014-12-11 | 2017-08-01 | 阿科玛法国公司 | 用于制备l‑氯‑2,2‑二氟乙烷的方法 |
CN107207388A (zh) * | 2015-02-17 | 2017-09-26 | 阿科玛法国公司 | 用于分离2‑氯‑1,1‑二氟乙烷和反式‑二氯乙烯的方法 |
CN108137316A (zh) * | 2014-10-31 | 2018-06-08 | 索尔维公司 | 包括氟化金属氧化物的催化剂,生产方法和氢化方法 |
CN109475841A (zh) * | 2016-05-23 | 2019-03-15 | 巴斯夫公司 | 铬催化剂、其制备和用途 |
CN109790089A (zh) * | 2016-09-27 | 2019-05-21 | 阿科玛法国公司 | 制备1-氯-2,2-二氟乙烷的方法 |
CN109803945A (zh) * | 2016-10-12 | 2019-05-24 | 阿科玛法国公司 | 包含1-氯-2,2-二氟乙烷和1,1-二氯乙烯的组合物 |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3014099B1 (fr) * | 2013-12-04 | 2017-01-13 | Arkema France | Procede de fabrication du 1-chloro-2,2,-difluoroethane |
FR3056589B1 (fr) * | 2016-09-27 | 2020-05-08 | Arkema France | Composition comprenant du 1-chloro-2,2-difluoroethane |
CN109804006A (zh) * | 2016-09-27 | 2019-05-24 | 阿科玛法国公司 | 包含1-氯-2,2-二氟乙烷的组合物 |
FR3056586B1 (fr) * | 2016-09-27 | 2020-05-08 | Arkema France | Composition comprenant du 1-chloro-2,2-difluoroethane |
FR3056585B1 (fr) * | 2016-09-27 | 2020-05-08 | Arkema France | Composition comprenant du 1-chloro-2,2-difluoroethane |
FR3056588B1 (fr) * | 2016-09-27 | 2018-10-12 | Arkema France | Composition comprenant du 1-chloro-2,2-difluoroethane |
FR3056590B1 (fr) * | 2016-09-27 | 2020-05-08 | Arkema France | Composition comprenant du 1-chloro-2,2-difluoroethane |
JP7444719B2 (ja) * | 2020-07-10 | 2024-03-06 | ダイキン工業株式会社 | 2-クロロ-1,1-ジフルオロエタン(hcfc-142)、1,1,2-トリフルオロエタン(hfc-143)、及び(e)-1,2-ジフルオロエチレン(hfo-1132(e))及び/又は(z)-1,2-ジフルオロエチレン(hfo-1132(z))の製造方法 |
CN114733529A (zh) * | 2022-03-18 | 2022-07-12 | 润泰化学(泰兴)有限公司 | 一种用于异丁酸和乙酸制备甲基异丙基酮的催化剂的制备方法和应用 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1008574A1 (en) * | 1998-12-08 | 2000-06-14 | Elf Atochem North America, Inc. | Preparation of 1-chloro-2,2-difluoroethane ("142") |
EP1008575A1 (en) * | 1998-12-08 | 2000-06-14 | Elf Atochem North America, Inc. | Preparation of 1-chloro-2,2-difluoroethane ("142") |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4139568A (en) * | 1978-05-22 | 1979-02-13 | The Dow Chemical Company | Process for making methyl fluoride |
JPS6226239A (ja) * | 1985-05-28 | 1987-02-04 | イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− | フルオロオレフインの接触ハロゲン交換法 |
GB9104775D0 (en) | 1991-03-07 | 1991-04-17 | Ici Plc | Fluorination catalyst and process |
DE69212821T2 (de) * | 1991-03-20 | 1996-12-19 | Du Pont | Verfahren zur herstellung von 2-chlor-1,1,1-trifluorethan |
US5300711A (en) * | 1991-03-20 | 1994-04-05 | E. I. Du Pont De Nemours And Company | Process for the manufacture of 2,2-dichloro-1,1,1-trifluoroethane, 2-chloro-1,1,1,2-tetrafluoroethane and pentafluoroethane |
GB9204072D0 (en) * | 1992-02-26 | 1992-04-08 | Ici Plc | Fluorination catalyst and process |
CN1037097C (zh) * | 1992-12-12 | 1998-01-21 | 浙江省化工研究院 | 由1,1-二氯乙烯液相氟化制1,1-二氯-1-氟乙烷 |
FR2700766B1 (fr) * | 1993-01-27 | 1995-03-24 | Atochem Elf Sa | Procédé de fluoration de perchloréthylène ou du pentachloréthane. |
GB9404703D0 (en) * | 1993-03-24 | 1994-04-27 | Ici Plc | Production of difluoromethane |
JPH09255596A (ja) * | 1996-03-22 | 1997-09-30 | Showa Denko Kk | 低級パーフルオロアルカンの製造方法 |
FR2783820A1 (fr) | 1998-09-03 | 2000-03-31 | Atochem Elf Sa | Procede de fabrication du 1-chloro-2,2-difluoro-ethane |
GB2375974B (en) | 2000-03-31 | 2004-08-11 | Council Scient Ind Res | A process for the preparation of 1, 1, 1, 2-tetrafluoroethane |
JP4314391B2 (ja) * | 2005-07-07 | 2009-08-12 | 独立行政法人産業技術総合研究所 | フッ素化触媒とその製造方法及びそれら触媒を用いたフッ素化合物の製造方法 |
CN1911512B (zh) * | 2005-07-07 | 2011-12-07 | 独立行政法人产业技术综合研究所 | 氟化催化剂及其制备方法、以及使用了该催化剂的氟化合物的制备方法 |
WO2008030442A1 (en) * | 2006-09-05 | 2008-03-13 | E. I. Du Pont De Nemours And Company | Processes for producing 1,2,3,3,3-pentafluoropropene and precursors thereof |
EP2341040B1 (en) | 2008-09-25 | 2017-09-06 | Central Glass Company, Limited | Process for producing 1,3,3,3-tetrafluoropropene |
-
2012
- 2012-10-11 EP EP12772776.6A patent/EP2766117B1/en active Active
- 2012-10-11 CN CN201280049801.6A patent/CN103842075B/zh active Active
- 2012-10-11 WO PCT/EP2012/070126 patent/WO2013053800A2/en active Application Filing
- 2012-10-11 IN IN2632CHN2014 patent/IN2014CN02632A/en unknown
- 2012-10-11 KR KR1020147011113A patent/KR101999136B1/ko active IP Right Grant
- 2012-10-11 TW TW101137387A patent/TWI615194B/zh active
- 2012-10-11 JP JP2014535069A patent/JP6078073B2/ja active Active
- 2012-10-11 MX MX2014004098A patent/MX340808B/es active IP Right Grant
- 2012-10-11 DK DK12772776.6T patent/DK2766117T3/en active
- 2012-10-11 BR BR112014008902-7A patent/BR112014008902B1/pt active IP Right Grant
- 2012-10-11 US US14/350,838 patent/US9000242B2/en active Active
- 2012-10-11 ES ES12772776.6T patent/ES2674149T3/es active Active
-
2014
- 2014-03-27 IL IL231760A patent/IL231760A/en active IP Right Grant
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1008574A1 (en) * | 1998-12-08 | 2000-06-14 | Elf Atochem North America, Inc. | Preparation of 1-chloro-2,2-difluoroethane ("142") |
EP1008575A1 (en) * | 1998-12-08 | 2000-06-14 | Elf Atochem North America, Inc. | Preparation of 1-chloro-2,2-difluoroethane ("142") |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108137316A (zh) * | 2014-10-31 | 2018-06-08 | 索尔维公司 | 包括氟化金属氧化物的催化剂,生产方法和氢化方法 |
CN107001196A (zh) * | 2014-12-11 | 2017-08-01 | 阿科玛法国公司 | 用于制备l‑氯‑2,2‑二氟乙烷的方法 |
CN107001196B (zh) * | 2014-12-11 | 2020-05-26 | 阿科玛法国公司 | 用于制备l-氯-2,2-二氟乙烷的方法 |
CN104692997A (zh) * | 2015-02-11 | 2015-06-10 | 巨化集团技术中心 | 一种1,1-二氟-2-氯乙烷的制备方法 |
CN104692998A (zh) * | 2015-02-11 | 2015-06-10 | 巨化集团技术中心 | 1,1-二氟-2-氯乙烷的制备方法 |
CN104692997B (zh) * | 2015-02-11 | 2017-12-22 | 巨化集团技术中心 | 一种1,1‑二氟‑2‑氯乙烷的制备方法 |
CN104692998B (zh) * | 2015-02-11 | 2018-06-26 | 巨化集团技术中心 | 1,1-二氟-2-氯乙烷的制备方法 |
CN107207388A (zh) * | 2015-02-17 | 2017-09-26 | 阿科玛法国公司 | 用于分离2‑氯‑1,1‑二氟乙烷和反式‑二氯乙烯的方法 |
CN109475841A (zh) * | 2016-05-23 | 2019-03-15 | 巴斯夫公司 | 铬催化剂、其制备和用途 |
CN109790089A (zh) * | 2016-09-27 | 2019-05-21 | 阿科玛法国公司 | 制备1-氯-2,2-二氟乙烷的方法 |
CN109803945A (zh) * | 2016-10-12 | 2019-05-24 | 阿科玛法国公司 | 包含1-氯-2,2-二氟乙烷和1,1-二氯乙烯的组合物 |
Also Published As
Publication number | Publication date |
---|---|
KR20140077941A (ko) | 2014-06-24 |
ES2674149T3 (es) | 2018-06-27 |
DK2766117T3 (en) | 2018-06-25 |
IL231760A (en) | 2017-06-29 |
IN2014CN02632A (zh) | 2015-08-07 |
US20140330051A1 (en) | 2014-11-06 |
IL231760A0 (en) | 2014-05-28 |
TWI615194B (zh) | 2018-02-21 |
WO2013053800A2 (en) | 2013-04-18 |
MX340808B (es) | 2016-07-27 |
BR112014008902B1 (pt) | 2020-03-10 |
KR101999136B1 (ko) | 2019-07-11 |
EP2766117A2 (en) | 2014-08-20 |
EP2766117B1 (en) | 2018-03-21 |
TW201321078A (zh) | 2013-06-01 |
BR112014008902A2 (pt) | 2017-05-09 |
CN103842075B (zh) | 2016-08-17 |
MX2014004098A (es) | 2014-05-21 |
JP6078073B2 (ja) | 2017-02-08 |
WO2013053800A3 (en) | 2013-06-06 |
US9000242B2 (en) | 2015-04-07 |
JP2014534899A (ja) | 2014-12-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103842075A (zh) | 1,1,2-三氯乙烷和/或1,2-二氯乙烯催化气相氟化制备1-氯-2,2-二氟乙烷 | |
JP4309627B2 (ja) | ジメチルエーテルの製造方法 | |
CN104428273B (zh) | 用于制造含氟烯烃的方法 | |
CN103189338A (zh) | 联合生产反式-1-氯-3,3,3-三氟丙烯、反式-1,3,3,3-四氟丙烯和1,1,1,3,3-五氟丙烷的集成方法 | |
US20110201851A1 (en) | Process for preparing 2,3,3,3-tetrafluoropropene | |
US11939277B2 (en) | Continuous preparation method of 2,3,3,3-tetrafluoropropene | |
WO2014094587A1 (zh) | 一种制备1,3,3,3-四氟丙烯的工艺 | |
CN103319303B (zh) | 一种同时制备1,1,1,2-四氟乙烷和二氟甲烷的方法 | |
WO2022028236A1 (zh) | 一种气相催化合成二氟甲烷的方法 | |
CN114605225A (zh) | 一种连续合成1,1,1,3,3-五氯丙烷的方法 | |
CN111848331A (zh) | 一种气相氟化合成2-氯-3,3,3-三氟丙烯的方法 | |
CN101723797A (zh) | 一种气相催化生产四氟甲烷的方法 | |
EP0460138B1 (en) | Method for producing chloroform | |
JP4424479B2 (ja) | キシリレンジアミンの製造方法 | |
JPH1053544A (ja) | ジフルオロメタンの製造のためのプロセス | |
CN101412654B (zh) | 一种1,1-二氟乙烷的制备方法及氟化催化剂 | |
CN102336630A (zh) | 一种2,3-二氯-1,1,1-三氟丙烷的催化合成方法 | |
CN116143583B (zh) | 一种2,3,3,3-四氟丙烯和1,3,3,3-四氟丙烯的联产制备方法 | |
CN115646480B (zh) | 1-氯-3,3,3-三氟丙烯制备用催化剂及其制备方法和应用 | |
Quan et al. | Synthesis of a porous chromium fluoride catalyst with a large surface area | |
CN1640860A (zh) | 制备氢氟烃的方法 | |
CN102065999A (zh) | 制备氟化化合物的方法 | |
WO2018015828A1 (en) | Process for high-pressure hydrogenation of carbon dioxide to syngas in the presence of used chromium oxide supported catalysts | |
CN112243434A (zh) | 生产2,3,3,3-四氟丙烯的方法和用于进行该方法的系统 | |
JPS58128329A (ja) | 塩化メチルの製造法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CP03 | Change of name, title or address | ||
CP03 | Change of name, title or address |
Address after: 50 Alfred Nobel Street, Monheim, Rhine, Germany 40789 Patentee after: BAYER INTELLECTUAL PROPERTY GmbH Address before: Germany Patentee before: BAYER INTELLECTUAL PROPERTY GmbH |
|
TR01 | Transfer of patent right | ||
TR01 | Transfer of patent right |
Effective date of registration: 20240111 Address after: 50 Alfred Nobel Street, Monheim, Rhine, Germany 40789 Patentee after: BAYER CROPSCIENCE AG Address before: 50 Alfred Nobel Street, Monheim, Rhine, Germany 40789 Patentee before: BAYER INTELLECTUAL PROPERTY GmbH |