WO2010101198A1 - Processus de préparation de propènes contenant du fluor renfermant du 2,3,3,3-tétrafluoropropène et du 1,3,3,3-tétrafluoropropène - Google Patents

Processus de préparation de propènes contenant du fluor renfermant du 2,3,3,3-tétrafluoropropène et du 1,3,3,3-tétrafluoropropène Download PDF

Info

Publication number
WO2010101198A1
WO2010101198A1 PCT/JP2010/053476 JP2010053476W WO2010101198A1 WO 2010101198 A1 WO2010101198 A1 WO 2010101198A1 JP 2010053476 W JP2010053476 W JP 2010053476W WO 2010101198 A1 WO2010101198 A1 WO 2010101198A1
Authority
WO
WIPO (PCT)
Prior art keywords
tetrafluoropropene
chromium oxide
catalyst
fluoropropane
tetrachloro
Prior art date
Application number
PCT/JP2010/053476
Other languages
English (en)
Inventor
Masatoshi Nose
Tsuneo Yamashita
Akinari Sugiyama
Original Assignee
Daikin Industries, Ltd.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Daikin Industries, Ltd. filed Critical Daikin Industries, Ltd.
Priority to JP2011537769A priority Critical patent/JP2012519654A/ja
Publication of WO2010101198A1 publication Critical patent/WO2010101198A1/fr

Links

Classifications

    • 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
    • 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

Definitions

  • the present invention relates to a process for preparing fluorine-containing propenes containing 2,3,3,3- tetrafluoropropene and 1, 3, 3, 3-tetrafluoropropene .
  • Non-Patent Literature 1 listed below; it is a single step method carried out by reacting a compound represented by CF 3 CF 2 CH 2 X (X is Cl or I) with zinc in ethanol.
  • NPL Non-Patent Literature 1 listed below; it is a single step method carried out by reacting a compound represented by CF 3 CF 2 CH 2 X (X is Cl or I) with zinc in ethanol.
  • this method is not suitable for industrial-scale production, because zinc is expensive and a large amount of waste is generated.
  • Methods for producing HFC-1234yf are also reported in other publications.
  • Patent Literature (PTL) 1 discloses a method comprising reacting chloromethyl tetrafluoropropanate with an amine
  • Patent Literature (PTL) 2 discloses a method comprising thermal decomposition of 1-trifluoromethyl-l, 2, 2- trifluorocyclobutane
  • Non-Patent Literatures (NPL) 2 and 3 listed below also disclose HFC-1234yf production methods.
  • these methods need to be improved for industrial usage because the starting materials are difficult to produce and are not easily obtained, the yield is low, multiple steps are required, etc.
  • Patent Literature (PTL) 5 discloses a method for producing HFC-1234ze comprising dehydrohalogenation of CF 3 CH 2 CHFX (wherein X is F, Cl, Br, or I) .
  • Patent Literature (PTL) 5 discloses a method comprising reacting CY 3 CH 2 CHY 2 (wherein Y is F, Cl, Br, or I) with HF (hydrogen fluoride) in the presence of a catalyst such as Cr 2 O 3 .
  • NPL 1 J. Chem. Soc, 1957, 2193-2197
  • NPL 3 J. Fluorine Chem., 1997, 82, 171-174
  • a primary object of the present invention is to provide an industrially applicable, simple and effective process for preparing fluorine-containing propenes containing 2, 3, 3, 3-tetrafluoropropene and 1,3,3,3- tetrafluoropropene .
  • Fluorine- containing propenes containing 2, 3, 3, 3-tetrafluoropropene (HFC- 1234yf) and 1, 3, 3, 3-tetrafluoropropene (HFC-1234ze) can be prepared in a single step reaction by reacting 1,1,1,3- tetrachloro-3-fluoropropane (HCFC-241fb) with anhydrous hydrogen fluoride in a gas phase in the presence of a catalyst. This reaction process can be used as an industrially advantageous method for producing these compounds.
  • the present invention has been accomplished based on these findings.
  • the present invention provides the following processes for preparing fluorine-containing propenes containing 2,3,3, 3-tetrafluoropropene and 1,3,3,3- tetrafluoropropene .
  • a process for preparing fluorine-containing propenes containing 2,3,3, 3-tetrafluoropropene and 1,3,3,3- tetrafluoropropene comprising reacting 1, 1, 1, 3-tetrachloro-3- fluoropropane represented by the formula CCl 3 CH 2 CHClF and anhydrous hydrogen fluoride in a gas phase in the presence of a catalyst.
  • chromium oxide further contains at least one metal element selected from the group consisting of indium, gallium, cobalt, nickel, zinc, and aluminum.
  • chromium oxide containing at least one metal element selected from the group consisting of indium, gallium, cobalt, nickel, zinc, and aluminum is a compound obtained by a method comprising a step of forming a precipitate from an aqueous solution containing chromium ions and metal ions.
  • 1, 1, 1, 1, 3-tetrachloro-3-fluoropropane is a reaction product of carbon tetrachloride and vinyl fluoride.
  • HCFC-241fb 1, 1, 1, 3-tetrachloro-3- fluoropropane represented by the formula CCl 3 CH 2 CHClF and anhydrous hydrogen fluoride (HF) are used as starting materials.
  • 1, 1, 1, 3-tetrachloro-3-fluoropropane which is one of the starting materials, is a known substance, and can be easily obtained, for example, by reacting carbon tetrachloride with vinyl fluoride. Carbon tetrachloride and vinyl fluoride, which are used as starting materials in this production process, are relatively inexpensive substances, and the production process is simple. Accordingly, 1, 1, 1, 3-tetrachloro-3-fluoropropane, which is used as a starting material in the process of the present invention, is a substance that is available at low cost.
  • the reaction of carbon tetrachloride and vinyl fluoride to obtain 1, 1, 1, 3-tetrachloro-3-fluoropropane can be carried out in the presence of at least one component selected from the group consisting of metals and metal halides, optionally using a nonpolar solvent that is inert to the reaction, such as methylene chloride or carbon bisulfide.
  • a nonpolar solvent that is inert to the reaction such as methylene chloride or carbon bisulfide.
  • metals that can be used for the reaction include copper, iron, manganese, and the like.
  • metal halides examples include aluminium chloride, cuprous chloride, cupric chloride, ferric chloride, manganese chloride, and the like. Such metals and metal halides can be used singly or in a combination of two or more.
  • a pentavalent phosphorus compound such as trimethyl phosphate, trimethylphosphine, triethyl phosphate, triethylphosphine, or tributyl phosphate, can be used as a reaction accelerator in the reaction of carbon . tetrachloride and vinyl fluoride.
  • the amount of vinyl fluoride is typically about 0.1 to about 10 moles per mole of carbon tetrachloride.
  • the amount of at least one component selected from the group consisting of metals and metal halides is typically about 0.001 to about 2 moles per mole of carbon tetrachloride.
  • the amount of pentavalent phosphorus compound used as a reaction accelerator is typically about 0.1 to about 10 moles per mole of the total amount of metal and metal halide.
  • the reaction temperature during the reaction of carbon tetrachloride with vinyl fluoride is typically about room temperature to 150 0 C, and preferably about 8O 0 C to about 12O 0 C.
  • the reaction pressure may be atmospheric pressure, an increased pressure, or a reduced pressure.
  • the reaction is typically carried out in a hermetically sealed container under increased pressure.
  • Patent Literature (PTL) 5 discloses a method for producing HFC-1234ze by dehydrohalogenation of CF 3 CH 2 CHFX (wherein X is F, Cl, Br, or I) . This method is not considered to be effective for industrial purposes, because the reaction process is complicated and the starting materials are expensive. Furthermore, the only useful substance among the obtained products is HFC-1234ze.
  • the process of the present invention uses inexpensive starting materials, and can produce fluorine- containing propenes containing two types of useful compounds, i.e., 2, 3, 3, 3-tetrafluoropropene and 1, 3, 3, 3-tetrafluoropropene in a substantially single step reaction. Therefore, the process of the present invention is highly useful for industrial purposes. Catalyst
  • the catalyst used in the present invention is not particularly limited, and any catalyst that is effective in the fluorination reaction with hydrogen fluoride can be used.
  • catalysts include metal oxides, metal halides, transition metals, etc.
  • the chromium oxide is a compound represented by the composition formula CrO 1n , wherein m is preferably in the range of 1.5 ⁇ m ⁇ 3, more preferably 1.8 ⁇ m ⁇ 2.5, and particularly preferably 2.0 ⁇ m ⁇ 2.3.
  • m is excessively small, the catalytic activity and selectivity of HFC-1234yf and HFC-1234ze tend to decrease, whereas if m is excessively large, the deterioration of the catalyst tends to progress, neither of which is desirable.
  • One example of a method for preparing the above chromium oxide is as follows.
  • an aqueous solution of a chromium salt e.g., chromium nitrate, chromium chloride, chromium alum, chromium sulfate, etc.
  • aqueous ammonia e.g., chromium nitrate, chromium chloride, chromium alum, chromium sulfate, etc.
  • 10% aqueous ammonia is added dropwise to a 5.7% aqueous solution of chromium nitrate in an amount of about 1 to about 1.2 equivalents per equivalent of chromium nitrate to precipitate chromium hydroxide.
  • the properties of chromium hydroxide can be controlled by varying the reaction rate during precipitation.
  • reaction rate varies depending on the temperature of the reaction solution, method of mixing aqueous ammonia (mixing speed) , stirring conditions, etc. Therefore, the reaction rate can be suitably adjusted by- controlling these conditions.
  • the precipitate is filtered, washed, and then dried.
  • the drying may be performed, for example, in air at about 70 0 C to about 200 0 C, and particularly at about 120 0 C, for about 1 to about 100 hours, and particularly for about 12 hours.
  • the product obtained at this stage is referred to as being in the form of chromium hydroxide.
  • This product is subsequently disintegrated into a powder.
  • the rate of precipitation is adjusted so that the density of the disintegrated powder (for example, a particle size of 1,000 um or less, and 95% of the powder having a size between 46 to 1,000 um) falls within a range of about 0.6 to about 1.1 g/ml, and preferably about 0.6 to about 1.0 g/ml.
  • a powder density of less than 0.6 g/ml is not preferable, because the pellet strength is weakened. Conversely, a powder density of more than 1.1 g/ml is not preferable, because the catalytic activity- is lowered, and the pellets break easily.
  • the specific surface area of the powder determined at 200°C with 80 minutes of degassing is preferably about 100 m 2 /g or more, and more preferably about 120 m 2 /g or more.
  • the upper limit of the specific surface area is, for example, about 220 m 2 /g. In the present specification, the specific surface area is measured by the BET method.
  • not more than approximately 3 wt.% of graphite may be mixed into the thus-obtained chromium hydroxide powder.
  • the resulting mixture is formed into pellets using a tableting machine.
  • the size of the pellets may be about 3.0 mm in diameter and about 3.0 mm in height.
  • the pellets preferably have a compressive strength (pellet strength) of about 210 ⁇ 40 kg/cm 2 . If the compressive strength is excessively high, the gas contact efficiency decreases and thus lowers the catalytic activity, and the pellets break easily. Conversely, if the compressive strength is excessively low, the resulting pellets are liable to be powdered and thereby become difficult to handle.
  • the resulting pellets are calcined in an inert atmosphere, for example, in a nitrogen gas stream, to produce an amorphous chromium oxide.
  • the calcination temperature is preferably not lower than 360 0 C. However, because chromium oxide is crystallized at exceedingly high temperatures, setting the calcination temperature at the highest possible temperature within the range that the crystallization of chromium oxide can be avoided is desirable.
  • the pellets may be calcined at a temperature of about 380 0 C to about 460 0 C, and particularly about 400 0 C, for about 1 to about 5 hours, and particularly for about 2 hours.
  • the calcined chromium oxide may have a specific surface area of about 170 m 2 /g or more, preferably about 180 m 2 /g or more, and more preferably about 200 m 2 /g or more.
  • the upper limit of the specific surface area is generally about 240 m 2 /g, and preferably about 220 m 2 /g. If the specific surface area is more than 240 m 2 /g, the catalytic activity is high but the deterioration rate increases. If the specific surface area is less than 170 m 2 /g, the catalytic activity becomes undesirably low.
  • Fluorinated chromium oxide can be prepared by the method disclosed in Japanese Unexamined Patent Publication No. 1993-146680.
  • fluorinated chromium oxide can be prepared by subjecting the chromium oxide obtained by the above- described method to fluorination (HF treatment) with hydrogen fluoride.
  • the fluorination temperature may be suitably selected within a range in which the water generated does not condense (for example, about 150 0 C at 0.1 MPa); the upper limit is the temperature at which the catalyst does not crystallize due to the reaction heat.
  • the pressure during fluorination is not particularly limited, but the fluorination may preferably be conducted at the same pressure as the pressure at which the catalyst will be used in a catalytic reaction.
  • the fluorination temperature is, for example, in the range of about 100 0 C to about 46O 0 C.
  • the surface area of the catalyst decreases as a result of fluorination. Generally, a greater specific surface area results in higher catalytic activity.
  • the specific surface area of the catalyst after fluorination is preferably about 25 to about 130 m 2 /g, and more preferably about 40 to about 100 m 2 /g, but it is not limited to the above range.
  • the fluorination reaction of chromium oxide may be conducted by supplying hydrogen fluoride to a reactor containing chromium oxide, prior to carrying out the process of the invention described later.
  • the reaction for producing 2,3,3,3- tetrafluoropropene and 1, 3, 3, 3-tetrafluoropropene can be conducted by supplying 1, 1, 1, 3-tetrachloro-3-fluoropropane, which is a starting material, to the reactor.
  • a fluorinated chromium oxide having a fluorine content of about 10 to about 30 wt.% can be preferably used.
  • the chromium-based catalyst (hereinafter, sometimes referred to as a "metal component-containing chromium catalyst") disclosed in Japanese Unexamined Patent Publication No. 11-171806 is usable as a chromium oxide catalyst or a fluorinated chromium oxide catalyst in the present invention.
  • This chromium- based catalyst is amorphous and mainly comprises a chromium compound containing at least one metal element selected from the group consisting of indium, gallium, cobalt, nickel, zinc, and aluminum, wherein the average valence of the chromium in the chromium compound is +3.5 or more and +5.0 or less.
  • the method for producing the metal component-containing chromium catalyst is not particularly limited.
  • the catalyst may be impregnated with an aqueous solution containing at least one metal element described above and then calcined to produce a metal component-containing chromium catalyst.
  • the following process is particularly preferable.
  • a compound containing a metal element described above is added to an aqueous solution of a chromium salt to prepare an aqueous solution containing chromium ions and metal ions .
  • the compound containing at least one metal element selected from the group consisting of indium, gallium, cobalt, nickel, zinc, and aluminum can be selected from compounds that are soluble in an aqueous solution containing a chromium salt.
  • a chromium salt for example, halides, nitrates, sulfates, and like water-soluble compounds can be used.
  • the amount of metal element is preferably about 0.1 to about 50 wt.%, and more preferably about 1.0 to about 30 wt.%, based on the total amount of the final metal component-containing chromium catalyst.
  • the metal component-containing chromium catalyst thus obtained may be fluorinated in the same manner as described above.
  • reaction process According to the process of the present invention, the reaction may typically be performed by supplying 1,1,1,3- tetrachloro-3-fluoropropane and anhydrous hydrogen fluoride as starting materials in a gas phase to a reactor containing a catalyst as mentioned above, whereby a reaction product containing 2, 3, 3, 3-tetrafluoropropene (HFC-1234yf) and 1,3,3,3- tetrafluoropropene (£-HFC-1234ze + Z-HFC-1234ze) can be obtained in a single step reaction.
  • HFC-1234yf 2, 3, 3, 3-tetrafluoropropene
  • 1,3,3,3- tetrafluoropropene £-HFC-1234ze + Z-HFC-1234ze
  • the ratio of 1, 1, 1, 3-tetrachloro-3-fluoropropane to anhydrous hydrogen fluoride, which are used as starting materials in the invention, is not particularly limited.
  • the amount of hydrogen fluoride may be at least 3 moles, and preferably at least 5 moles, per mole of 1, 1, 1, 3-tetrachloro-3- fluoropropane .
  • the upper limit of the amount of hydrogen fluoride is preferably about 20 moles, and more preferably about 15 moles per mole of 1, 1, 1, 3-tetrachloro-3-fluoropropane.
  • the starting materials may be supplied to the reactor as is, or may be diluted with an inert gas such as nitrogen, helium, or argon and then supplied to the reactor.
  • an inert gas such as nitrogen, helium, or argon
  • the starting materials may be supplied to the reactor together with oxygen.
  • the amount of oxygen is preferably about 0.1 mol% to about 5 mol%, based on the total number of moles of 1, 1, 1, 3-tetrachloro-3-fluoropropane and anhydrous hydrogen fluoride.
  • the type of the reactor used in the process of the invention is not particularly limited.
  • examples of usable reactors include an adiabatic reactor containing a catalyst, a multitubular reactor cooled using a heat transfer medium, etc.
  • the reaction temperature i.e., the temperature in the reactor is preferably about 170 0 C to about 450 0 C, and more preferably about 210°C to about 400 0 C. If the reaction temperature is higher than this range, the catalytic activity decreases. Conversely, if the reaction temperature is lower than this range, the starting material conversion and the selectivity of 1,3,3,3- tetrafluoropropene become undesirably low.
  • the pressure during the reaction is not particularly limited, and the reaction may be conducted under normal pressure or increased pressure. More specifically, the reaction of the invention can be performed at atmospheric pressure (0.1 MPa), but may be performed at an increased pressure of up to about 1.0 MPa.
  • the reaction time is not particularly limited. However, the contact time, which is determined by W/F o , may typically be adjusted to a range of about 2 to about 30 g-sec/cc, and preferably about 4 to about 15 g-sec/cc.
  • W/F o is a ratio of a catalyst weight W (g) to a total flow rate F 0 (flow rate at 0 0 C, 0.1 MPa: cc/sec) of starting material gases that are introduced to a reaction system.
  • the total flow rate F 0 refers to the flow rate of 1, 1, 1, 2-tetrachloro-3-fluoropropane and hydrogen fluoride that are supplied as starting materials, or the flow rate of these starting materials plus the flow rate of an inert gas and/or an oxygen gas, when such gases are also supplied.
  • a reaction product containing 2,3,3,3- tetrafluoropropene (HFC-1234yf) and 1, 3, 3, 3-tetrafluoropropene (£-HFC-1234ze + Z-HFC-1234ze) can be obtained from the reactor outlet.
  • 1, 3, 3, 3-tetrafluoropropene is obtained as a mixture of E- and Z-isomers.
  • the selectivity of 2,3,3,3- tetrafluoropropene is about 2 to about 5%, and the selectivity of 1, 3, 3, 3-tetrafluoropropene (£-HFC-1234ze + Z-HFC- 1234ze) can be increased to 25% or more by appropriately selecting the catalyst and reaction conditions.
  • the reaction product may be used as is or can be separated and purified by distillation etc. to separately recover 2, 3, 3, 3-tetrafluoropropene and 1, 3, 3, 3-tetrafluoropropene.
  • Other fluorine-containing olefins may be converted into other compounds in a subsequent reaction step.
  • unreacted CCl 3 CH 2 CHClF (HCFC-241fb) when present, may be returned to the reactor after isolation and purification, and can be used as a starting material again. Therefore, high productivity can be maintained even if the conversion of the starting material is low because the unreacted starting material can be recycled.
  • the target fluorine-containing propenes containing 2,3,3,3- tetrafluoropropene (HFC-1234yf) and 1, 3, 3, 3-tetrafluoropropene (£-HFC-1234ze + Z-HFC-1234ze) can be obtained in a single step reaction by using readily available 1, 1, 1, 3-tetrachloro-3- fluoropropane and hydrogen fluoride as starting materials.
  • a 1000-ml autoclave equipped with a thermometer, a vacuum line, a nitrogen purge line, a feeding line, a gauge, and a pressure release valve was filled with 4.5 g (79.2 mmol) of soft iron powder, 20 g (79.2 mmol) of triethyl phosphate, 100 mg of ferric chloride, and 420 g (2.73 mol) of carbon tetrachloride.
  • the autoclave was purged five times with nitrogen, and once with vinyl fluoride.
  • the autoclave was subsequently evacuated, and vinyl fluoride was introduced thereinto with stirring until a gauge pressure of 0.4 MPa was reached. When the autoclave was heated to 120 0 C, a reaction began.
  • the internal temperature increased to 127°C, and the internal pressure decreased from 0.9 MPa to 0.4 MPa. While the pressure of vinyl fluoride was maintained at 0.8 MPa, stirring was continued at an internal temperature of 120°C for 8 hours. Then, 10 g (39.6 mmol) of triethyl phosphate was injected into the autoclave, and the reaction was further allowed to proceed at 120 0 C for 10 hours.
  • a tubular Hastelloy reactor with an inner diameter of 20 mm and a length of 1 m was charged with 42.7 g of a catalyst (fluorine content: about 16.4 wt.%) obtained by fluorinating a chromium oxide represented by the composition formula CrO 2-O -
  • the reactor was maintained at atmospheric pressure (0.1
  • Example 3 An experiment was conducted under the same conditions as in Example 1 except that 42.7 g of a catalyst (fluorine content: about 17.8 wt.%) obtained by fluorinating a chromium oxide represented by the composition formula CrO 2-2 was used. The molar ratio of HF to 1, 1, 1, 3-tetrachloro-3-fluoropropane was 15, and the contact time (W/F0) was 8.0 g-sec/cc. Table 1 shows the results of the analysis.
  • a catalyst fluorine content: about 17.8 wt.% obtained by fluorinating a chromium oxide represented by the composition formula CrO 2-2 was used.
  • the molar ratio of HF to 1, 1, 1, 3-tetrachloro-3-fluoropropane was 15, and the contact time (W/F0) was 8.0 g-sec/cc. Table 1 shows the results of the analysis.
  • Example 3 shows the results of the analysis.
  • Example 4 An experiment was conducted under the same conditions as in Example 1 except that 36.7 g of a catalyst obtained by fluorinating a chromium oxide represented by the composition formula CrOi. 9 was used, the flow rate of anhydrous hydrogen fluoride was changed to 200 cc/min (0°C, 0.1 MPa), and the reaction temperature was changed to 300 0 C. The molar ratio of HF to 1, 1, 1, 3-tetrachloro-3-fluoropropane was 10, and the contact time (W/Fo) was 10.0 g-sec/cc. Table 1 shows the results of the analysis.
  • Example 4 shows the results of the analysis.
  • Example 1 An experiment was conducted under the same conditions as in Example 1 except that the amount of the catalyst was changed to 35.0 g, the flow rate of the anhydrous hydrogen fluoride (HF) gas was changed to 400 cc/min (flow rate at O 0 C and 0.1 MPa), and the reaction temperature was changed to 380 0 C.
  • the molar ratio of HF to 1, 1, 1, 3-tetrachloro-3-fluoropropane was 20, and the contact time (W/F o ) was 5.0 g-sec/cc. Table 1 shows the results of the analysis.
  • Example 5 An experiment was conducted under the same conditions as in Example 1 except that 42.7 g of a catalyst (fluorine content: about 13.9 wt.%) obtained by fluorinating a chromium oxide represented by the composition formula CrOi -6 was used. The molar ratio of HF to 1, 1, 1, 3-tetrachloro-3-fluoropropane was 15, and the contact time (W/F o ) was 8.0 g-sec/cc. Table 1 shows the results of the analysis.
  • Example 6 shows the results of the analysis.
  • the resulting solid chromium hydroxide was pulverized to a particle size of 0.2 mm or less to produce 63.4 g of a chromium hydroxide powder. Subsequently, 2.5 wt.% of graphite was added to this powder, and the resulting powder was compression-molded into cylindrical pellets having a diameter of 3 mm and a height of 3 mm. The pellets were calcined at 400 0 C for 2 hours in a nitrogen gas stream to yield 46.0 g of a nickel-containing chromium oxide.
  • the valence number of Cr of the nickel-containing chromium oxide determined from magnetic susceptibility measurements was CrO 2-O - Further, the results of X-ray diffraction analysis (XRD) confirmed that this catalyst is amorphous.
  • the specific surface area of the catalyst was 187.1 m 2 /g.
  • the weight ratio of the metals contained in the obtained catalyst was calculated from SEM (scanning electron microscopic) analysis results.
  • the ratio of Ni to Cr was 20.2 to 79.8.
  • the reactor was maintained at atmospheric pressure (0.1 MPa) and 250 0 C, and a supply of anhydrous hydrogen fluoride (HF) gas at 200 cc/min (flow rate at 0 0 C and 0.1 MPa) and nitrogen (N 2 ) at 100 cc/min (flow rate at 0°C and 0.1 MPa) to the reactor was maintained for 2 hours.
  • HF hydrous hydrogen fluoride
  • N 2 nitrogen
  • 1, 1, 1, 3-tetrachloro-3-fluoropropane (HCFC-241fb, purity: 98.9%) was supplied at a rate of 20 cc/min (flow rate at 0 0 C and 0.1 MPa), and the temperature of the reactor was changed to 300°C.
  • the molar ratio of HF to 1, 1, 1, 3-tetrachloro-3-fluoropropane was

Abstract

La présente invention concerne un processus de préparation de propènes contenant du fluor renfermant du 2,3,3,3-tétrafluoropropène et du 1,3,3,3-tétrafluoropropène, ledit processus consistant à faire réagir du 1,1,1,3-tétrachloro-3-fluoropropane représenté par la formule CCl3CH2CHClF et du fluorure d'hydrogène anhydre en phase gazeuse en présence d'un catalyseur. Le processus selon la présente invention permet de produire des propènes contenant du fluor renfermant du 2,3,3,3-tétrafluoropropène et du 1,3,3,3-tétrafluoropropène de manière simple, efficace et applicable dans l'industrie.
PCT/JP2010/053476 2009-03-04 2010-02-25 Processus de préparation de propènes contenant du fluor renfermant du 2,3,3,3-tétrafluoropropène et du 1,3,3,3-tétrafluoropropène WO2010101198A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2011537769A JP2012519654A (ja) 2009-03-04 2010-02-25 ２，３，３，３−テトラフルオロプロペンと１，３，３，３−テトラフルオロプロペンを含む含フッ素プロペンの製造方法

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US15736809P 2009-03-04 2009-03-04
US61/157,368 2009-03-04

Publications (1)

Publication Number Publication Date
WO2010101198A1 true WO2010101198A1 (fr) 2010-09-10

Family

ID=42316059

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2010/053476 WO2010101198A1 (fr) 2009-03-04 2010-02-25 Processus de préparation de propènes contenant du fluor renfermant du 2,3,3,3-tétrafluoropropène et du 1,3,3,3-tétrafluoropropène

Country Status (2)

Country Link
JP (1) JP2012519654A (fr)
WO (1) WO2010101198A1 (fr)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102603460A (zh) * 2012-02-20 2012-07-25 西安近代化学研究所 一种2-氯-1,1,1,2-四氟丙烷的制备方法
WO2013015068A1 (fr) * 2011-07-26 2013-01-31 Daikin Industries, Ltd. Procédé de préparation de 2,3,3,3-tétrafluoropropène
WO2013122822A1 (fr) 2012-02-14 2013-08-22 Honeywell International Inc. Procédé pour la production de 1,3,3,3-tétrafluoropropène
CN103896725A (zh) * 2012-12-24 2014-07-02 中化蓝天集团有限公司 一种制备2,3,3,3-四氟丙烯和2-氯-3,3,3-三氟丙烯的方法
JP2014528912A (ja) * 2011-07-08 2014-10-30 アルケマ フランス ２，３，３，３−テトラフルオロプロペンおよびフッ化水素酸を分離し回収する方法
EP2421811B1 (fr) 2009-04-23 2016-08-03 Daikin Industries, Ltd. Procédé de préparation de 2,3,3,3-tétrafluoropropène
US10392326B2 (en) 2015-01-21 2019-08-27 Daikin Industries, Ltd. Method for producing fluorine-containing compound
EP3699164A4 (fr) * 2017-10-19 2021-07-28 Zhejiang Quhua Fluor-Chemistry Co Ltd Procédé de co-production de 2,3,3,3-tétrafluoropropylène et de trans-1,3,3,3-tétrafluoropropylène

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7029093B2 (ja) * 2020-09-01 2022-03-03 セントラル硝子株式会社 トランス－１－クロロ－３，３，３－トリフルオロプロペンの製造方法

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2931840A (en) 1958-11-25 1960-04-05 Du Pont Process for preparing 2, 3, 3, 3-tetrafluoropropene
US3996299A (en) 1973-02-08 1976-12-07 Phillips Petroleum Company Fluoro compound preparation
JPS63211245A (ja) 1987-02-27 1988-09-02 Daikin Ind Ltd ２，３，３，３−テトラフルオロプロペンの製法
JPH05146680A (ja) 1991-05-24 1993-06-15 Daikin Ind Ltd フツ素化触媒およびハロゲン化炭化水素のフツ素化方法
WO1997005089A1 (fr) * 1995-08-01 1997-02-13 E.I. Du Pont De Nemours And Company Procedes de fabrication d'halocarbures et de composes selectionnes, et azeotropes formes avec hf
JPH11140002A (ja) 1997-11-11 1999-05-25 Central Glass Co Ltd １，３，３，３−テトラフルオロプロペンの製造法
JPH11171806A (ja) 1997-12-12 1999-06-29 Daikin Ind Ltd ペンタフルオロエタンの製造方法、並びにフッ素化用触媒及びその製造方法
EP0974571A2 (fr) 1998-07-21 2000-01-26 Elf Atochem North America, Inc. Préparation du 1,1,1,3-tétrafluoropropène (1234ze)
US20050245773A1 (en) 2004-04-29 2005-11-03 Honeywell International Inc. Processes for synthesis of 1,3,3,3-tetrafluoropropene
WO2005108334A1 (fr) 2004-04-29 2005-11-17 Honeywell International, Inc. Procedes pour la synthese de 1,3,3,3-tetrafluoropropene et de 2,3,3,3-tetrafluoropropene
US20060258891A1 (en) 2005-05-12 2006-11-16 Honeywell International Inc. Method for producing fluorinated organic compounds
US20070129579A1 (en) 2003-07-25 2007-06-07 Honeywell International Inc. Processes for selective dehydrohalogenation of halogenated alkanes
JP2007320896A (ja) 2006-05-31 2007-12-13 Central Glass Co Ltd １，３，３，３−テトラフルオロプロペンの製造方法
WO2008002499A2 (fr) 2006-06-27 2008-01-03 E. I. Du Pont De Nemours And Company Procédés de production de tétrafluoropropène
WO2008002500A1 (fr) 2006-06-27 2008-01-03 E. I. Du Pont De Nemours And Company Procédés de production de tétrafluoropropène
US20080051611A1 (en) 2006-08-24 2008-02-28 Honeywell International Inc. PROCESS FOR THE PRODUCTION OF HFO TRANS-1234ze FROM HFC-245fa

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2931840A (en) 1958-11-25 1960-04-05 Du Pont Process for preparing 2, 3, 3, 3-tetrafluoropropene
US3996299A (en) 1973-02-08 1976-12-07 Phillips Petroleum Company Fluoro compound preparation
JPS63211245A (ja) 1987-02-27 1988-09-02 Daikin Ind Ltd ２，３，３，３−テトラフルオロプロペンの製法
JPH05146680A (ja) 1991-05-24 1993-06-15 Daikin Ind Ltd フツ素化触媒およびハロゲン化炭化水素のフツ素化方法
WO1997005089A1 (fr) * 1995-08-01 1997-02-13 E.I. Du Pont De Nemours And Company Procedes de fabrication d'halocarbures et de composes selectionnes, et azeotropes formes avec hf
JPH11140002A (ja) 1997-11-11 1999-05-25 Central Glass Co Ltd １，３，３，３−テトラフルオロプロペンの製造法
JPH11171806A (ja) 1997-12-12 1999-06-29 Daikin Ind Ltd ペンタフルオロエタンの製造方法、並びにフッ素化用触媒及びその製造方法
EP0974571A2 (fr) 1998-07-21 2000-01-26 Elf Atochem North America, Inc. Préparation du 1,1,1,3-tétrafluoropropène (1234ze)
US20070129579A1 (en) 2003-07-25 2007-06-07 Honeywell International Inc. Processes for selective dehydrohalogenation of halogenated alkanes
US20050245773A1 (en) 2004-04-29 2005-11-03 Honeywell International Inc. Processes for synthesis of 1,3,3,3-tetrafluoropropene
WO2005108334A1 (fr) 2004-04-29 2005-11-17 Honeywell International, Inc. Procedes pour la synthese de 1,3,3,3-tetrafluoropropene et de 2,3,3,3-tetrafluoropropene
US20060258891A1 (en) 2005-05-12 2006-11-16 Honeywell International Inc. Method for producing fluorinated organic compounds
JP2007320896A (ja) 2006-05-31 2007-12-13 Central Glass Co Ltd １，３，３，３−テトラフルオロプロペンの製造方法
WO2008002499A2 (fr) 2006-06-27 2008-01-03 E. I. Du Pont De Nemours And Company Procédés de production de tétrafluoropropène
WO2008002500A1 (fr) 2006-06-27 2008-01-03 E. I. Du Pont De Nemours And Company Procédés de production de tétrafluoropropène
US20080051611A1 (en) 2006-08-24 2008-02-28 Honeywell International Inc. PROCESS FOR THE PRODUCTION OF HFO TRANS-1234ze FROM HFC-245fa

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
J. CHEM. SOC., vol. 1957, pages 2193 - 2197
J. CHEM. SOC., vol. 3, 1970, pages 414 - 421
J. FLUORINE CHEM., vol. 82, 1997, pages 171 - 174

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2421811B1 (fr) 2009-04-23 2016-08-03 Daikin Industries, Ltd. Procédé de préparation de 2,3,3,3-tétrafluoropropène
JP2016179977A (ja) * 2011-07-08 2016-10-13 アルケマ フランス ２，３，３，３−テトラフルオロプロペンおよびフッ化水素酸を分離し回収する方法
JP2014528912A (ja) * 2011-07-08 2014-10-30 アルケマ フランス ２，３，３，３−テトラフルオロプロペンおよびフッ化水素酸を分離し回収する方法
US8772554B2 (en) 2011-07-26 2014-07-08 Daikin Industries, Ltd. Process for preparing 2,3,3,3-tetrafluoropropene
CN103717560A (zh) * 2011-07-26 2014-04-09 大金工业株式会社 用于制备2,3,3,3-四氟丙烯的方法
JP2014523395A (ja) * 2011-07-26 2014-09-11 ダイキン工業株式会社 ２，３，３，３−テトラフルオロプロペンの製造方法
WO2013015068A1 (fr) * 2011-07-26 2013-01-31 Daikin Industries, Ltd. Procédé de préparation de 2,3,3,3-tétrafluoropropène
CN108033871A (zh) * 2012-02-14 2018-05-15 霍尼韦尔国际公司 1,3,3,3-四氟丙烯的制备
WO2013122822A1 (fr) 2012-02-14 2013-08-22 Honeywell International Inc. Procédé pour la production de 1,3,3,3-tétrafluoropropène
US8889924B2 (en) * 2012-02-14 2014-11-18 Honeywell International Inc. Process for the production of 1,3,3,3-tetrafluoropropene
CN104159878A (zh) * 2012-02-14 2014-11-19 霍尼韦尔国际公司 1，3，3，3-四氟丙烯的制备
EP2814797A4 (fr) * 2012-02-14 2015-10-14 Honeywell Int Inc Procédé pour la production de 1,3,3,3-tétrafluoropropène
CN102603460A (zh) * 2012-02-20 2012-07-25 西安近代化学研究所 一种2-氯-1,1,1,2-四氟丙烷的制备方法
CN103896725A (zh) * 2012-12-24 2014-07-02 中化蓝天集团有限公司 一种制备2,3,3,3-四氟丙烯和2-氯-3,3,3-三氟丙烯的方法
CN103896725B (zh) * 2012-12-24 2016-01-20 中化蓝天集团有限公司 一种制备2,3,3,3-四氟丙烯和2-氯-3,3,3-三氟丙烯的方法
WO2014101685A1 (fr) * 2012-12-24 2014-07-03 中化近代环保化工(西安)有限公司 Procédé de préparation de 2,3,3,3-tétrafluoropropène et de 2-chloro-3,3,3-trifluoropropène
US10392326B2 (en) 2015-01-21 2019-08-27 Daikin Industries, Ltd. Method for producing fluorine-containing compound
EP3699164A4 (fr) * 2017-10-19 2021-07-28 Zhejiang Quhua Fluor-Chemistry Co Ltd Procédé de co-production de 2,3,3,3-tétrafluoropropylène et de trans-1,3,3,3-tétrafluoropropylène

Also Published As

Publication number Publication date
JP2012519654A (ja) 2012-08-30

Similar Documents

Publication Publication Date Title
US8614361B2 (en) Process for preparation of 2,3,3,3-tetrafluoropropene
US8198491B2 (en) Process for preparing 2,3,3,3-tetrafluoropropene and 1,3,3,3-tetrafluoropropene
WO2010101198A1 (fr) Processus de préparation de propènes contenant du fluor renfermant du 2,3,3,3-tétrafluoropropène et du 1,3,3,3-tétrafluoropropène
US8344191B2 (en) Process for preparing 2,3,3,3-tetrafluoropropene
JP5831589B2 (ja) 含フッ素アルケン化合物の製造方法
US20110201851A1 (en) Process for preparing 2,3,3,3-tetrafluoropropene
EP2326612B1 (fr) Procédé de préparation de 2,3,3,3-tétrafluoropropène
JP5413451B2 (ja) ２，３，３，３−テトラフルオロプロペンの製法
EP2632882A1 (fr) Procédé de production de 2,3,3,3-tétrafluoropropène
JP6753434B2 (ja) ジフルオロエチレンの製造方法
KR20140114897A (ko) 불소-함유 올레핀의 제조방법
JP5246327B2 (ja) 気相フッ素化による含フッ素プロペンの製造方法
US8865952B2 (en) Process for producing fluorine-containing alkene

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 10708828

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2011537769

Country of ref document: JP

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 10708828

Country of ref document: EP

Kind code of ref document: A1