Classifications

• • 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
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C17/00—Preparation of halogenated hydrocarbons
  • C07C17/23—Preparation of halogenated hydrocarbons by dehalogenation
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C17/00—Preparation of halogenated hydrocarbons
  • C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C17/00—Preparation of halogenated hydrocarbons
  • C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
  • C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
  • C07C17/278—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of only halogenated hydrocarbons

Definitions

• the present invention relates to processes that involve the production of halogenated hydrocarbon products comprising 2,3,3,3- tetrafluoropropene.
• HFC-1234yf has been prepared by reaction of CH 2 CIC 2 F 5 with zinc in ethanol as reported by Haszeldine and Steele in Journal of the Chemical Society, pages 2193- 2197 (1957) or as a by-product in the vapor phase fluorination of 3-chloro- 1 ,1 ,2,2-tetrafluoropropane over chromium catalysts as disclosed by Yasuhara, et. al. in U. S. Patent No. 5,629,461.
• the present invention provides a process for making HFC- 1234yf employing a multi-step process.
• HCFC-225ca is dehydrofluorinated over a suitable catalyst for a time sufficient to convert at least a portion of HCFC-225ca to CFC-1214ya.
• HCFC-225ca may be prepared by reacting CCI 3 CF 2 CF 3 (CFC- 215cb) with hydrogen as disclosed by Baker in U. S. Patent No. 5,300,712.
• the dehydrofluorination reaction may be conducted in the vapor phase in a reaction zone containing the dehydrofluorination catalyst at temperatures of from about 200 0 C to about 500 0 C and preferably from about 300 0 C to about 45O 0 C.
• the contact time is typically from about 1 to about 450 seconds, preferably from about 10 to about 120 seconds.
• the reaction pressure can be subatmospheric, atmospheric or superatmospheric. Generally, near atmospheric pressures are preferred. However, the dehydrofluorination of HCFC-225ca can be beneficially run under reduced pressure (i.e., pressures less than one atmosphere).
• the catalytic dehydrofluorination can optionally be carried out in the presence of an inert gas such as nitrogen, helium or argon.
• an inert gas such as nitrogen, helium or argon.
• the addition of an inert gas can be used to increase the extent of dehydrofluorination.
• the mole ratio of inert gas to HCFC-225ca is from about 5:1 to 1 :1.
• Nitrogen is the preferred inert gas.
• Typical dehydrofluorination reaction conditions and dehydrofluorination catalysts are disclosed in U.S. Patent No. 5,396,000, which is incorporated herein by reference in its entirety.
• the dehydrofluorination catalyst comprises at least one catalyst selected from the group consisting of carbon, aluminum fluoride, fluorided alumina, trivalent chromium oxide, and trivalent chromium chloride, fluoride, or chlorofluoride preferably supported on a support such as carbon, aluminum fluoride, or fluorided alumina.
• the effluent from the dehydrofluorination reactor typically includes HF 1 CFC-1214ya, some CFC-1215yb and CF 3 CHFCCI 2 F (HCFC-225eb), and any unconverted HCFC-225ca.
• the CFC-1214ya may be separated from the product mixture formed in the dehydrofluorination reactor by methods known to the art.
• this separation can also include isolation of azeotrope or near azeotrope composition of CFC-
• HF-free CFC-1214ya may be obtained using procedures similar to those disclosed in U.S. Patent Application Publication No.
• Unreacted HCFC-225ca can be recycled back to the dehydrofluorination reactor.
• CFC-1214ya is hydrogenated over a suitable catalyst.
• Catalysts suitable for carrying out the process of making HFC- 1234yf from CFC-1214ya in accordance with this invention comprise palladium and may optionally comprise additional Group VIII metals (e.g., Pt, Ru, Rh or Ni).
• the palladium is supported on alumina, fluorided alumina, aluminum fluoride or a mixture thereof.
• the palladium-containing precursor used to prepare the catalyst is preferably a palladium salt (e.g., palladium chloride). Other metals, when used, may be added to the support during the preparation of the catalyst.
• the supported metal catalysts may be prepared by conventional methods known in the art such as by impregnation of the carrier with a soluble salt of the catalytic metal (e.g., palladium chloride or rhodium nitrate) as described by Satterfield on page 95 of Heterogenous Catalysis in Industrial Practice, 2 nd edition (McGraw-Hill, New York, 1991). Palladium supported on alumina is available commercially. A suitable procedure for preparing a catalyst containing palladium on fluorided alumina is described in U. S. Patent No. 4,873,381 , which is incorporated herein by reference.
• a soluble salt of the catalytic metal e.g., palladium chloride or rhodium nitrate
• a catalytically effective amount is meant the concentration of catalysts on the support that is sufficient to carry out the catalytic reaction.
• concentration of palladium on the support is typically in the range of from about 0.1% to about 10% by weight based on the total weight of the catalyst and is preferably in the range of about 0.1 % to about 5% by weight based on the total weight of the catalyst.
• concentration of the additional Group VIII metal, when used, is about 3% by weight, or less, based on the total weight of the catalyst; but palladium is ordinarily at least 50% by weight based on the weight of the total metals present on the support, and preferably at least 80% by weight based on the weight of the total metals present on the support.
• the relative amount of hydrogen fed during contact of CFC-1214ya in a reaction zone containing the palladium-containing catalyst is from about 1 mole of H2 per mole of CFC-1214ya to about 4 moles of H 2 per mole of CFC-1214ya, preferably from about 1 mole of H 2 per mole of CFC- 1214ya to about 3 moles of H 2 per mole of CFC-1214ya and more preferably from about 1 mole of H 2 per mole of CFC-1214ya to about 2 moles H 2 per mole of CFC-1214ya.
• the reaction zone temperature for the catalytic hydrogenation of CFC-1214ya is typically in the range of from about 100 0 C to about 400 0 C, and preferably is in the range of from about 125°C to about 350 0 C.
• the contact time is typically in the range of from about 1 to about 450 seconds, and preferably is in the range of from about 10 to about 120 seconds.
• the reactions are typically conducted at near atmospheric pressure.
• the desired HFC-1234yf is separated by methods known to the art.
• the unreacted CFC-1214ya and HCFC-1224yd, the product of intermediate hydrogenation, can be recycled back to the hydrogenation reactor
• the reactor, distillation columns, and their associated feed lines, effluent lines, and associated units used in applying the process of this invention should be constructed of materials resistant to hydrogen fluoride and hydrogen chloride.
• Typical materials of construction, well-known to the fluorination art, include stainless steels, in particular of the austenitic
• TM type the well-known high nickel alloys, such as Monel nickel-copper alloys, Hastelloy nickel-based alloys and, lnconel nickel-chromium alloys, and copper-clad steel.
• An lnconelTM tube (5/8 inch OD (1.59 cm)) is charged with a commercial sample of 25 weight percent chromium(lll) chloride supported on carbon (10 cc, 3.4 g, 12-20 mesh (1.68-0.84 mm)).
• the tube is connected to a reactor system and surrounded with an electrically-heated furnace.
• the catalyst is then activated by purging with nitrogen (37.5 seem , 6.2x10 "7 mVs) at 300 0 C for 2 hours.
• the catalyst is then fluorinated with a 3:1 mixture of nitrogen and hydrogen fluoride (total flow 35 seem, 5.8x10 "7 m 3 /s) as the temperature in the reactor is increased from 300 0 C to 425 0 C over the course of 9 hours.
• the ratio of nitrogen to hydrogen fluoride is then changed from 3:1 to 0:4 with a total flow rate of 35 seem (5.8x10 "7 m 3 /s) over the course of 3 hours at 425 0 C.
• the flow of HF is then stopped and the reactor tube cooled to about 350 0 C under a nitrogen flow.
• a mixture of HCFC-225ca and nitrogen (molar ratio 1 :3) is then passed through the catalyst bed at 350°C with a contact time of about 30 seconds.
• the pressure in the reactor is nominally atmospheric.
• Analysis of the reactor effluent shows at least 50% or the HCFC-225ca is converted with CFC-1214ya being the major reaction product.
• the effluent also contains unreacted starting material and lesser amounts of C 3 HCI 3 F 4 and C 3 HCIF 6 isomers.
• the reactor is allowed to cool to 15O 0 C, and then hydrogen gas (20 seem, 3.3x10 '7 m 3 /s) is passed into the reactor for three hours as the temperature in the reactor is increased to 300°C.
• the reactor is cooled again to 150 0 C under a flow of nitrogen (20 seem, 3.3x10 "7 m 3 /s).
• the catalyst is then fluorinated with mixture of nitrogen and hydrogen fluoride according to following sequence (time in hours, flow rate nitrogen, flow rate HF, temperature): 2 h, 7.5x10 '7 m 3 /s, 8.3x10 "8 m 3 /s, 150°C; 2 h, 6.6x10 "7 m 3 /s, 1.7x10 "7 m 3 /s, 150°C; 2 h, 6.6x10 "7 mVs, UxiO '7 m 3 /s, 200°C; 2 h, 6.6x10 "7 m 3 /s, 1.7x10 "7 m 3 /s, 250°C; 2 h, 4.2x10 "7 m 3 /s, 4.2x10 "7 m 3 /s, 4.2x10 "7 m 3 /s, 25O 0 C.
• the flow of hydrogen fluoride is then stopped and the reactor is purged with nitrogen.

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• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

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• 2007
  • 2007-11-14 TW TW096143109A patent/TW200837036A/zh unknown
  • 2007-11-15 JP JP2009537221A patent/JP5570219B2/ja active Active
  • 2007-11-15 US US12/444,526 patent/US7872161B2/en active Active
  • 2007-11-15 WO PCT/US2007/024061 patent/WO2008060614A2/en not_active Ceased

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