EP3762353A1 - Verfahren zur herstellung von 2,3,3,3-tetrafluorpropen - Google Patents
Verfahren zur herstellung von 2,3,3,3-tetrafluorpropenInfo
- Publication number
- EP3762353A1 EP3762353A1 EP19715969.2A EP19715969A EP3762353A1 EP 3762353 A1 EP3762353 A1 EP 3762353A1 EP 19715969 A EP19715969 A EP 19715969A EP 3762353 A1 EP3762353 A1 EP 3762353A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- stream
- catalyst
- tetrafluoropropene
- carried out
- electrical conductivity
- 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.)
- Pending
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
-
- 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
- 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
Definitions
- the present invention relates to the production of hydrofluoroolefins. More particularly, the present invention relates to the production of 2,3,3,3-tetrafluoropropene.
- Halogenated hydrocarbons particularly fluorinated hydrocarbons such as hydrofluoroolefins, are compounds which have a useful structure as functional materials, solvents, refrigerants, blowing agents and monomers for functional polymers or starting materials for such monomers.
- Hydrofluoroolefins such as 2,3,3,3-tetrafluoropropene (HFO-1234yf) are attracting attention because they offer promising behavior as low global warming potential refrigerants.
- the processes for producing fluoroolefins are usually carried out in the presence of a starting material such as an alkane containing chlorine or a chlorine-containing alkene, and in the presence of a fluorinating agent such as hydrogen fluoride. These processes can be carried out in the gas phase or in the liquid phase, in the absence or absence of catalyst.
- US 2009/0240090 discloses a gas phase process for the preparation of 2-chloro-3,3,3-trifluoropropene (HCFO-1233xf) from 1,1,1,2,3-pentachloropropane (HCC -240db).
- HCFO-1233xf 2-chloro-3,3,3-trifluoropropene
- HCC -240db 1,1,1,2,3-pentachloropropane
- a 2,3,3,3-tetrafluoropropene preparation process comprising in particular a step of contacting 2-chloro-3,3,3-trifluoropropene with HF in the gas phase in the presence of a fluorination catalyst.
- the present invention relates to a process for the production of 2,3,3,3-tetrafluoropropene comprising the steps of: a) providing a stream A comprising at least one starting compound selected from the group consisting of 2-chloro-3,3,3-trifluoropropene and 2,3-dichloro-1,1,1-trifluoropropane,
- step a) characterized in that the electrical conductivity of said stream A supplied in step a) is less than 15 mS / cm.
- the present process optimizes and improves the production of 2,3,3,3-tetrafluoropropene.
- An electrical conductivity value of less than 15 mS / cm of the current A before the fluorination and / or dehydrofluorination step is carried out makes it possible to guarantee optimum efficiency of the reaction in terms of conversion and selectivity. If a catalyst is present, such a value also ensures optimal catalyst efficiency.
- step b) is carried out in the gaseous phase in the presence of a catalyst.
- the electrical conductivity of said current A is less than 10 mS / cm.
- step b) is carried out in the presence of a chromium-based catalyst, in particular said catalyst comprises a chromium oxyfluoride or a chromium oxide or a chromium fluoride or a mixture of them.
- the catalyst is based on chromium and also comprises a co-catalyst selected from the group consisting of Ni, Zn, Co, Mn or Mg, preferably the content of cocatalyst is between 0, 01% and 10% based on the total weight of the catalyst.
- stream A comprises 2-chloro-3,3,3-trifluoropropene, HF and optionally 1,1,1,2,2-pentafluoropropane.
- the stream B comprises, besides 2,3,3,3-tetrafluoropropene, HF, HCl, unreacted 2-chloro-3,3,3-trifluoropropene and optionally 1,1,1 , 2,2-pentafluoropropane.
- step b) is carried out at a temperature of between 310 ° C. and 420 ° C.
- step b) is carried out in the presence of hydrofluoric acid having an electrical conductivity of less than 10 mS / cm.
- the present invention relates to a process for producing 2,3,3,3-tetrafluoropropene comprising the steps of:
- the electrical conductivity of said current A supplied in step a) is less than 15 mS / cm.
- the electrical conductivity of said current A supplied in step a) is less than 14 mS / cm, preferably less than 13 mS / cm, more preferably less than 12 mS / cm, in particular less than 11 mS / cm, more especially less than 10 mS / cm, preferably less than 9 mS / cm, advantageously preferred less than 8 mS / cm, preferentially preferred less than 7 mS / cm, more preferably preferred less than 6 mS / cm cm, particularly preferably less than 5 mS / cm.
- the electrical conductivity is measured using an inductive conductivity measuring cell and according to the practice known to those skilled in the art.
- the measurement of the electrical conductivity is carried out at ambient temperature.
- the measurement of the electrical conductivity is carried out at a pressure equal to the pressure at which step b) is implemented.
- the electrical conductivity of the current A can be decreased to reach a conductivity of less than 15 ms / cm by decreasing the concentration of electrolyte possibly present therein according to the techniques known to those skilled in the art (distillation, cooling and decantation, passage over 3 to 5 A molecular sieves or zeolites).
- the measuring cell is coated with a material resistant to a corrosive medium, in particular resistant to hydrofluoric acid.
- the electrical conductivity of said current A is measured prior to step b).
- the electrical conductivity of said current A is measured when it is in liquid form.
- Said method according to the present invention may therefore comprise a step of heating and vaporization of said stream A prior to the implementation of step b) to supply said stream A in gaseous form.
- said stream A implemented in step b) is in gaseous form when it is brought into contact with HF.
- step b) is carried out in the presence of a catalyst, preferably a chromium-based catalyst.
- a catalyst preferably a chromium-based catalyst.
- the chromium-based catalyst may be a chromium oxide (for example CrO 2, CrC 3 or Cr 2 C 3), an oxyfluoride of chromium or a chromium fluoride (eg CrFs) or a mixture thereof.
- the chromium oxyfluoride may contain a fluorine content of between 1 and 60% by weight based on the total weight of the chromium oxyfluoride, advantageously between 5 and 55% by weight, preferably between 10 and 52% by weight, more preferably between 15 and 52% by weight, in particular between 20 and 50% by weight, more particularly between 25 and 45% by weight, preferably between 30 and 45% by weight, more preferably from 35 to 45% by weight. by weight of fluorine based on the total weight of the chromium oxyfluoride.
- the catalyst may also comprise a co-catalyst selected from the group consisting of Ni, Co, Zn, Mg, Mn, Fe, Zn, Ti, V, Zr, Mo, Ge, Sn, Pb, Sb; preferably Ni, Co, Zn, Mg, Mn; in particular Ni, Co, Zn.
- the content by weight of the cocatalyst is between 1 and 10% by weight based on the total weight of the catalyst.
- the catalyst can be supported or not.
- a carrier such as alumina, activated alumina, aluminum halides (AlF 3 for example), aluminum oxyhalides, activated carbon, magnesium fluoride or graphite can be used.
- the catalyst may have a specific surface area of between 70 and 225 m 2 / g, advantageously between 90 and 200 m 2 / g, preferably between 100 and 190 m 2 / g, in particular between 125 and 180 m 2 / g .
- the catalyst may have a specific surface area of between 1 and 100 m 2 / g, preferably between 5 and 80 m 2 / g, more preferably between 5 and 70 m 2 / g, ideally between 5 and 50 m 2 / g, in particular between 10 and 50 m 2 / g, more particularly between 15 and 45 m 2 / g.
- the pressure at which step b) is carried out is atmospheric pressure or a pressure greater than this, advantageously the pressure at which step b) is carried out is greater than 1.5 bara, preferably greater than 2.0 bara, in particular greater than 2.5 bara, more particularly greater than 3.0 bara.
- step b) is carried out at a pressure of between atmospheric pressure and 20 bara, preferably between 2 and 18 bara, more preferably between 3 and 15 bara.
- step b) of the present process is carried out with a contact time between 1 and 100 s, preferably between 2 and 75 s, in particular between 3 and 50 s.
- the HF molar ratio and said at least one of the compounds of said stream A ie 2-chloro-3,3,3-trifluoropropene or 2,3-dichloro-1,1,1-trifluoropropane, may vary between 1: 1 and 150: 1, preferably between 2: 1 and 125: 1, more preferably between 3: 1 and 100: 1.
- An oxidant such as oxygen or chlorine, can be added during step b).
- the molar ratio of the oxidant on the hydrocarbon compound may be between 0.005 and 2, preferably between 0.01 and 1.5.
- the oxidant may be pure oxygen, air or a mixture of oxygen and nitrogen.
- step b) is carried out at a temperature of between 310 ° C. and 420 ° C., advantageously between 310 ° C. and 400 ° C., preferably between 310 ° C. and 375 ° C. more preferably between 310 ° C and 360 ° C, in particular between 330 ° C and 360 ° C.
- stream A comprises 2-chloro-3,3,3-trifluoropropene or 2,3-dichloro-1,1,1-trifluoropropane, HF and optionally 1, 1,1,2,2- pentafluoropropane.
- the stream B comprises, besides 2, 3,3,3-tetrafluoropropene, HF, HCl, 2-chloro-3,3,3-trifluoropropene or 2,3-dichloro-1,1,1 unreacted trifluoropropane and optionally 1,1,1,2,2-pentafluoropropane.
- stream B is purified, preferably by distillation, to form a first stream comprising 2,3,3,3-tetrafluoropropene, HCl and optionally 1,1,1,2,2-pentafluoropropane, and a second stream comprising HF and 2-chloro-3,3,3-trifluoropropene or 2,3-dichloro-1,1,1-trifluoropropane.
- said stream B is distilled under conditions sufficient to form said first stream comprising 2,3,3,3-tetrafluoropropene, HCl and 1,1,1,2,2-pentafluoropropane, and said second stream comprising HF and 2 chloro-3,3,3-trifluoropropene.
- the distillation can be carried out at a pressure of 2 to 6 bara, more particularly at a pressure of 3 to 5 bara.
- the temperature at the top of the distillation column is from -35 ° C. to 10 ° C., preferably from -20 ° C. to 0 ° C.
- said stream B obtained in step b) is cooled prior to the purification mentioned above.
- said stream B obtained in step b) is cooled to a temperature below 100 ° C, and then distilled to form said first stream comprising 2,3,3,3-tetrafluoropropene, HCl and 1,1,1, 2,2-pentafluoropropane, and said second stream comprising HF and 2-chloro-3,3,3-trifluoropropene or 2,3-dichloro-1,1,1-trifluoropropane; the temperature at the top of the distillation column is -35 ° C. to 10 ° C. and the distillation is carried out at a pressure of 2 to 6 bara.
- Said stream B can be cooled, before distillation, to a temperature below 95 ° C, preferably below 90 ° C, preferably below 85 ° C, more preferably below 80 ° C, in particular below 70 ° C, more particularly lower than 60 ° C, preferably below 55 ° C, advantageously preferred lower than 50 ° C, preferably preferentially less than 40 ° C, more preferably preferably less than 30 ° C, particularly preferably less than 25 ° C, more preferably less than 20 ° C. Cooling the resulting product stream at such temperatures can facilitate subsequent distillation.
- the cooling of said stream B can be carried out by means of one or a plurality of heat exchangers.
- the cooling of said stream B can be carried out by passing it through one, two, three, four, five, six, seven, eight, nine or ten heat exchangers, preferably the number of heat exchangers is between 2 and 8, in particular between 3 and 7.
- step b) is carried out in the presence of hydrofluoric acid having an electrical conductivity of less than 10 mS / cm, preferably less than 5 mS / cm.
- the electrical conductivity of hydrofluoric acid can be measured prior to its use in step b) of the present process.
- the electrical conductivity of the hydrofluoric acid is measured before step b) and the hydrofluoric acid is in liquid form during the measurement.
- the method may also comprise a step of heating and vaporizing the hydrofluoric acid prior to the implementation of step b) to provide hydrofluoric acid in gaseous form.
- the hydrofluoric acid is in gaseous form when contacted with said stream A.
- the process according to the present invention is carried out continuously.
- the fluorination of HCFO-1233xf (2-chloro-3,3,3-trifluoropropene) to HFO-1234yf (2,3,3,3-tetrafluoropropene) and optionally to HFC-245cb (1,1,1,2,2 -pentafluoropropane) is carried out in a multitubular reactor.
- the reactor contains a mass catalyst based on chromium oxide.
- the catalyst is activated by a series of steps including drying, fluorination, air treatment and fluorination with recycling. This multi-step treatment makes the catalytic solid active and selective.
- the fluorination process is carried out according to the following operating conditions:
- a molar ratio between the HF and the sum of the organic feeds by the recycling loop between 15 and 20
- the process is carried out with a current of HCFO-1233xf having three different electrical conductivity values: 6, 10 and 35 mS / cm. Electrical conductivity was measured at room temperature and 5.8 bara. The run is stopped when the conversion to 2-chloro-3,3,3-trifluoropropene is less than 50%. Table 1 below shows the values obtained.
- the electrical conductivity of the HCFO-1233xf current is measured using a cell marketed by Endress + Hauser and referenced under the term InduMax P CLS 50 coated with a corrosive medium-resistant polymer-perfluoroalkoxy polymer (PFA) coating. containing HF.
- PFA corrosive medium-resistant polymer-perfluoroalkoxy polymer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1851956A FR3078699B1 (fr) | 2018-03-07 | 2018-03-07 | Procede de production du 2,3,3,3-tetrafluoropropene |
PCT/FR2019/050477 WO2019170989A1 (fr) | 2018-03-07 | 2019-03-04 | Procédé de production du 2,3,3,3-tétrafluoropropène |
Publications (1)
Publication Number | Publication Date |
---|---|
EP3762353A1 true EP3762353A1 (de) | 2021-01-13 |
Family
ID=62683343
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19715969.2A Pending EP3762353A1 (de) | 2018-03-07 | 2019-03-04 | Verfahren zur herstellung von 2,3,3,3-tetrafluorpropen |
Country Status (5)
Country | Link |
---|---|
US (1) | US11034635B2 (de) |
EP (1) | EP3762353A1 (de) |
CN (1) | CN111712479B (de) |
FR (1) | FR3078699B1 (de) |
WO (1) | WO2019170989A1 (de) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3023286B1 (fr) | 2014-07-02 | 2018-02-16 | Arkema France | Procede de fabrication de tetrafluoropropene |
HRP20231540T1 (hr) | 2017-03-10 | 2024-03-01 | The Chemours Company Fc, Llc | Postupak za pripremu 3,3,3-trifluoroprop-1-ena |
FR3078698B1 (fr) | 2018-03-07 | 2020-02-21 | Arkema France | Procede de production du 2-chloro-3,3,3-trifluoropropene |
FR3078700B1 (fr) | 2018-03-07 | 2020-07-10 | Arkema France | Procede de production du 2,3,3,3-tetrafluoropropene |
FR3081158B1 (fr) | 2018-05-16 | 2020-07-31 | Arkema France | Procede de production du 1-chloro-3,3,3-trifluoropropene. |
FR3083232B1 (fr) | 2018-06-27 | 2021-11-12 | Arkema France | Procede de production du 1-chloro-3,3,3-trifluoropropene |
FR3086287B1 (fr) | 2018-09-26 | 2020-09-18 | Arkema France | Stabilisation du 1-chloro-3,3,3-trifluoropropene |
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FR3068970B1 (fr) | 2017-07-17 | 2019-07-26 | Arkema France | Procede de production du 2,3,3,3-tetrafluoropropene. |
FR3068969B1 (fr) | 2017-07-17 | 2019-07-26 | Arkema France | Procede de production du 2,3,3,3-tetrafluoropropene. |
FR3078698B1 (fr) | 2018-03-07 | 2020-02-21 | Arkema France | Procede de production du 2-chloro-3,3,3-trifluoropropene |
FR3078700B1 (fr) | 2018-03-07 | 2020-07-10 | Arkema France | Procede de production du 2,3,3,3-tetrafluoropropene |
-
2018
- 2018-03-07 FR FR1851956A patent/FR3078699B1/fr active Active
-
2019
- 2019-03-04 EP EP19715969.2A patent/EP3762353A1/de active Pending
- 2019-03-04 US US16/976,819 patent/US11034635B2/en active Active
- 2019-03-04 WO PCT/FR2019/050477 patent/WO2019170989A1/fr unknown
- 2019-03-04 CN CN201980013476.XA patent/CN111712479B/zh active Active
Also Published As
Publication number | Publication date |
---|---|
WO2019170989A1 (fr) | 2019-09-12 |
FR3078699B1 (fr) | 2020-02-21 |
CN111712479B (zh) | 2024-08-13 |
US11034635B2 (en) | 2021-06-15 |
US20200407293A1 (en) | 2020-12-31 |
FR3078699A1 (fr) | 2019-09-13 |
CN111712479A (zh) | 2020-09-25 |
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