WO2014151441A1 - Process for producing 2,3,3,3-tetrafluoropropene - Google Patents
Process for producing 2,3,3,3-tetrafluoropropene Download PDFInfo
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- WO2014151441A1 WO2014151441A1 PCT/US2014/025733 US2014025733W WO2014151441A1 WO 2014151441 A1 WO2014151441 A1 WO 2014151441A1 US 2014025733 W US2014025733 W US 2014025733W WO 2014151441 A1 WO2014151441 A1 WO 2014151441A1
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/07—Preparation of halogenated hydrocarbons by addition of hydrogen halides
- C07C17/087—Preparation of halogenated hydrocarbons by addition of hydrogen halides to unsaturated halogenated hydrocarbons
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- 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
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/24—Chromium, molybdenum or tungsten
- B01J23/26—Chromium
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- 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
- B01J23/74—Iron group metals
- B01J23/745—Iron
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- 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
- B01J23/74—Iron group metals
- B01J23/75—Cobalt
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- 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
- B01J23/74—Iron group metals
- B01J23/755—Nickel
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- 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
- B01J27/08—Halides
- B01J27/10—Chlorides
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- 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
- B01J27/125—Halogens; Compounds thereof with scandium, yttrium, aluminium, gallium, indium or thallium
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- 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
- B01J27/128—Halogens; Compounds thereof with iron group metals or platinum group metals
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- 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
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- 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
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- 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 invention relates to a process to prepare 2-chloro-3,3,3-trifhioropropene (HCO- 1233xf) or 2-chloro-l,l,12-tetrafluoropropane (HCFC-244bb) using dichloro- trifluoropropanes and/or trichloro-difluoropropanes, and to prepare 2-chloro-3,3,3- trifluoropropene (HCO-1233xf) using various 242 and 243 isomers.
- HCO- 1233xf 2-chloro-3,3,3-trifhioropropene
- HCFC-244bb 2-chloro-l,l,12-tetrafluoropropane
- HFOs hydrofluoroolefins
- tetrafluoropropenes including 2,3,3,3- tetrafluoropropene (HFO-1234yf)
- HFO-1234yf 2,3,3,3- tetrafluoropropene
- HFO-1234yf has also been shown to be a low global warming compound with low toxicity and, hence, can meet increasingly stringent requirements for refrigerants in mobile air conditioning. Accordingly, compositions containing HFO-1234yf is a leader among the materials being developed for use in many of the aforementioned applications.
- U.S. Pat. No. 2,931,840 (Marquis) describes a method of making fluorine containing olefins by pyrolysis of methyl chloride and tetrafluoroethylene or chlorodifluoromethane. This process is a relatively low yield process and a very large percentage of the organic starting material is converted to unwanted and/or unimportant byproducts, including a sizeable amount of carbon black which tends to deactivate the catalyst used in the process.
- the preparation of HFO-1234yf from trifhioroacetylacetone and sulfur tetrafluoride has been described (See Banks, et al., Journal of Fluorine Chemistry, Vol. 82, Iss. 2, p. 171- 174 (1997)).
- U.S. Pat. No. 5,162,594 discloses a process wherein
- tetrafluoroethylene is reacted with another fluorinated ethylene in the liquid phase to produce a polyfluoroolefin product.
- dichlorotrifluoropropanes include, but are not limited to, 2,2-dichloro-l,l,l-trifluoropropane (HCFC-243ab), 2,3-dichloro- 1,1,1- trifluoropropane (HCFC-243db), l,2-dichloro-l,l,2-trifluoropropane (HCFC-243bc), and combinations thereof.
- Trichlorodifluoropropanes include, but are not limited to, 1,2,2- trichloro-l,l-difluoropropane (HCFC-242ac), l,l,2-trichloro-l,2-difluoropropane (HCFC- 242bc), l,2,3-trichloro-l,l-difluoropropane (HCFC-242dc), and combinations thereof.
- the present invention relates to a process for preparing 2-chloro-3,3,3,- trifluoropropene or 2-chloro-l,l,l,2-tetrafluoropropane that includes at least the following steps:
- dichlorotrifluoropropanes such as 2,2-dichloro- 1,
- the present invention relates to a process for preparing 2-chloro- 3,3,3-trifluoropropene by providing a starting composition including at least one compound of formula I, II, and/or III
- the by-products may include one or a combination of trichlorofluoropropene (1231) isomers, 2,3-dichloro-3,3- difluoropropene (1232xf), 2-chloro-l,l,l,2-tetrafluoropropane (244bb), 1,1,1,2,2- pentafluoropropane (245cb), dichlorotrifluoropropanes (243), trichlorodifluoropropanes (242).
- the dichlorotrifluoropropanes and trichlorodifluoropropanes may include, but are not limited to, one or a combination of those compounds identified above or otherwise herein.
- This final composition is then processed to separate desired products and recyclables from the remainder of the composition.
- 1233xf and HCl are first separated by feeding the composition into a recycle or distillation column. From such a column, the lighter components, such as 1233xf, 244bb (if any), 245cb (if any), HCl, and a portion of unreacted HF are isolated in a first or top stream, and the remaining organic components, such as unreacted HF, optional unreacted started compounds, one or more by-products (e.g. 242 and 243 isomers), and residual 1233xf are recovered in a second or bottom stream. From the top stream, 1233xf is purified using standard distillation methods, such as those provided herein. It is then forwarded to the second step of the reaction (discussed below) to produce 244bb and, ultimately, 1234yf.
- the bottom stream of the recycle or distillation column is then further processed to isolate recyclable compounds from the first reaction step.
- Unreacted HF for example, is substantially separated by phase separation.
- the second or bottom stream from the recycle column is provided to a phase separator where unreacted HF separates into a first layer.
- this first layer also includes, as a residual portion, certain of the organics such as, but not limited to, 1233xf, 1232xf, and 243.
- the remaining organics e.g. optional unreacted starting compound, residual 1233xf, and one or more by-products, which may include 1232xf, 242, and/or 243 are separated into a second layer.
- the HF-rich first layer is then extracted, optionally purified, and recycled.
- the second layer is similarly extracted and the unreacted starting material (if any) and recyclable products and/or byproducts purified for recycling.
- the purified byproducts preferably include at least one or more of the 242 and/or 243 isomers provided herein which are recycled to the first step fluorination reaction to produce 1233xf and/or 244bb.
- the final composition of the reaction includes each of at least 2-chloro-3,3,3-trifluoropropene (1233xf), HC1, unreacted HF, optional unreacted starting compound, trichlorofluoropropene (1231) isomers, 2,3-dichloro- 3,3-difluoropropene (1232xf), a first by-product selected from the group consisting of 1,1,1,2-tetrafluoropropane (244bb), 1,1,1,2,2-pentafluoropropane (245cb), and combinations thereof, and a second by-product selected from the group consisting of
- dichlorotrifluoropropane (243), trichlorodifluoropropane (242), and combinations thereof.
- the final composition is then fed into a recycle or distillation column, where the lighter components, such as 1233xf, first by-product(s), HC1, and a portion of unreacted HF are isolated from the column in a first or top stream.
- the remaining components such as unreacted HF, optional unreacted started compounds, residual 1233xf, trichlorofluoropropene (1231) isomers, 2,3-dichloro-3,3-difluoropropene (1232xf), second by-product(s) and third by-product(s) are recovered in a second or bottom stream.
- the 1233xf is purified using standard methods, such as those described herein, and forwarded to the second stage of the reaction to produce 244bb.
- the compounds in the bottom stream may then be further separated to isolate recyclable compounds from the first reaction step.
- Unreacted HF for example, is separated by phase separation.
- the second stream from the recycle column is provided to a phase separator where the majority of unreacted HF separates into a first layer.
- this first layer also includes, as a residual portion, certain of the organics such as, but not limited to, 1233xf, 1232xf, and 243.
- the remaining organics not provided in the first layer e.g. optional unreacted starting compound, residual amounts of 1233xf, 1231 isomers, 1232xf, and second and third by-product(s)
- a small portion of unreacted HF are separated into a second layer.
- the first layer which is rich in HF, is then extracted, optionally purified, and recycled.
- the optional unreacted starting compound, trichlorofluoropropene (1231) isomers, 2,3-dichloro-3,3-difluoropropene (1232xf), second by-product(s) e.g. 242 and/or 243 are separated from the third by-products by a high boiler purge system and are recycled.
- the optional unreacted starting compound, trichlorofluoropropene (1231) isomers, 2,3-dichloro-3,3-difluoropropene (1232xf), residual amounts of 1233xf and second by-product(s) may then be recycled to the reactor alone or in conjunction with the second by-products (e.g. 242 and/or 243).
- the present invention is further advantageous because it provides one or more process steps for improving the reaction efficiency used for the production of HFOs, such as 2- chloro-3,3,3,-trifluoropropene (1233xf) or, more broadly, for the production of 2,3,3,3- tetrafluoropropene (1234yf), of which 1233xf is a known intermediate. Additional embodiments and advantages to the present invention will be readily apparent to one of skill in the art, based on the disclosure provided herein.
- 243ab is converted to 1233xf which can be returned to the reaction to form 244bb.
- the conversion of 243ab to 1233xf is by dehydrochlorination using select catalysts, such as carbon solids, metal halides, halogenated metal oxides, zero metals, and the like.
- the 243ab is dehydrochlorinated in the reaction whereby 244bb is converted to 1234yf. The 243ab is concurrently converted to 1233xf which can then be reused as above.
- the invention is to a process to prepare 2-chloro-3,3,3- trifluoropropene (HCO-1233xf) or 2-chloro-l,l,12-tetrafluoropropane (HCFC-244bb) comprising contacting a compound selected from the group consisting of a dichloro- trifluoropropane, a trichloro-difluoropropane, and combinations thereof, with anhydrous hydrogen fluoride (HF) under conditions effective to produce 2-chloro-3,3,3-trifluoropropene (HCO-1233xf), 2-chloro-l,l,12-tetrafluoropropane (HCFC-244bb), or combinations thereof.
- HF hydrous hydrogen fluoride
- the process is practiced with the proviso that 2,3-dichloro- 1,1,1 - trifluoropropane (HCFC-243db) is excluded from the dichloro-trifluoropropanes when preparing HCO-1233xf.
- the invention is directed to process to prepare 2-chloro-l,l,12-tetrafluoropropane (HCFC-244bb) comprising contacting a compound selected from the group consisting of a dichloro-trifluoropropane, a trichloro- difluoropropane, and combinations thereof, with anhydrous hydrogen fluoride (HF) under conditions effective to produce HCFC-244bb.
- HF hydrous hydrogen fluoride
- the invention is to a process to prepare 2-chloro-3,3,3- trifluoropropene (HCO-1233xf) and 2-chloro-l,l,l,2-tetrafluoropropane (244bb) comprising a contacting step comprising contacting at least one compound of Formulae (I), (II), (III)
- X is independently selected from F, CI, Br, and I, provided that at least one X is not fluorine, with anhydrous hydrogen fluoride (HF) in the presence of a catalyst under conditions effective to form a composition comprising HCO-1233xf and a by-product selected from the group consisting of a dichloro-trifluoropropane, a trichloro-difluoropropane and combinations thereof; recovering the by-product from the composition; recycling the byproduct to the contacting step wherein the by-product is converted to 2-chloro-l,l,l,2- tetrafluoropropane (244bb).
- HF hydrous hydrogen fluoride
- the invention is to a process to prepare 2-chloro-3,3,3- trifluoropropene (HCO-1233xf) comprising contacting l,l,l-trifluoro-2,2-dichloropropane (243ab) with a dehydrochlorination catalyst under conditions effective to form 1233xf.
- the present invention relates to a manufacturing process for making 2,3,3, 3-tetrafluoroprop-l-ene using a starting material according to any one or combination of formulas I, II, and/or III:
- the compound(s) of Formula I, II and/or III contains at least one chlorine, a majority of the Xs as chlorine, or all Xs as chlorine.
- the compound(s) of formula I includes 1,1,2,3-tetrachloropropene (1230xa).
- the compound(s) of formula II includes 2,3,3, 3-tetrachloropropene (1230xf).
- the compound(s) of formula III include 1,1,1,2,3- pentachloropropane (240db).
- the method generally includes at least three reaction steps.
- a starting composition including compounds of Formula I, II, and/or III e.g. 1,1,2,3- tetrachloropropene, 2,3,3,3-tetrachloropropene, and/or 1,1,1,2,3-pentachloropropane
- anhydrous HF in a first vapor phase reactor (fluorination reactor) to produce a mixture of 2-chloro-3,3,3-trifluoropropene (1233xf) and HC1.
- the reaction occurs in the vapor phase in the presence of a vapor phase catalyst, such as, but not limited to, a fluorinated chromium oxide.
- the catalyst may (or may not) have to be activated with anhydrous hydrogen fluoride HF (hydrogen fluoride gas) before use depending on the state of the catalyst.
- fluorinated chromium oxides are disclosed as the vapor phase catalyst, the present invention is not limited to this embodiment. Any fluorination catalysts known in the art may be used in this process. Suitable catalysts include, but are not limited to chromium, aluminum, cobalt, manganese, nickel and iron oxides, hydroxides, halides, oxyhalides, inorganic salts thereof and their mixtures and any one of which may be optionally
- Combinations of catalysts suitable for the present invention nonexclusively include Cr 2 0 3 , FeCl 3 /C, Cr 2 0 3 /Al 2 0 3 , Cr 2 0 3 /A1F 3 , Cr 2 0 3 /carbon, CoCl 2 /Cr 2 0 3 /Al 2 0 3 , NiCl 2 /Cr 2 0 3 /Al 2 0 3 , CoCl 2 /AlF 3 , NiCl 2 /AlF 3 and mixtures thereof.
- Chromium (III) oxides such as crystalline chromium oxide or amorphous chromium oxide are preferred with amorphous chromium oxide being most preferred.
- Chromium oxide (Cr 2 0 3 ) is a commercially available material which may be purchased in a variety of particle sizes. Fluorination catalysts having a purity of at least 98% are preferred. The fluorination catalyst is present in an excess but in at least an amount sufficient to drive the reaction.
- This first step of the reaction may be conducted in any reactor suitable for a vapor phase fluorination reaction.
- the reactor is constructed from materials which are resistant to the corrosive effects of hydrogen fluoride and catalyst such as
- inert gases such as nitrogen or argon may be employed in the reactor during operation.
- the mol ratio of HF to 1230xa in step 1 of the reaction is 1: 1 to 50: 1, from about 10: 1 to about 50: 1, or from about 10: 1 to about 20: 1.
- the reaction between HF and 1230xa is carried out at a temperature from about 150°C to about 500°C, in certain embodiments, about 150°C to about 400°C, or about 150°C to about 300°C.
- the reaction pressure is about of about 0 psig to about 500 psig, in certain embodiments from about 20 psig to about 200 psig, or about 50 to about 100 psig.
- the mol ratio of HF to 1230xf in step 1 of the reaction is 1: 1 to 50: 1, from about 10: 1 to about 50: 1, or from about 10: 1 to about 20: 1.
- the reaction between HF and 1230xf is carried out at a temperature from about 150°C to about 500°C, in certain embodiments, about 150°C to about 400°C, or about 150°C to about 300°C.
- the reaction pressure is about of about 0 psig to about 500 psig, in certain embodiments from about 20 psig to about 200 psig, or about 50 to about 100 psig.
- the mol ratio of HF to 240db in step 1 of the reaction is 1: 1 to 50: 1, from about 10: 1 to about 50: 1, or from about 10: 1 to about 20: 1.
- the reaction between HF and 240db is carried out at a temperature from about 150°C to about 500°C, in certain embodiments, about 150°C to about 400°C, or about 150°C to about 300°C.
- the reaction pressure is about of about 0 psig to about 500 psig, in certain embodiments from about 20 psig to about 200 psig, or about 50 to about 100 psig.
- the fluorination reaction may be carried out to attain a single- or multi-pass conversion of at least 1% or higher, 5% or higher, 10% or higher or about 20% or higher.
- the starting reagent is converted to 1233xf in a single pass, wherein the reaction conditions achieve a conversion amount greater than 75%, greater than 85%, greater than 95% or greater than 99%.
- the resulting effluent includes small or trace amounts of unreacted starting material or may be substantially free of such compounds.
- the effluent from the fluorination reaction step including any intermediate effluents that may be present in multi-stage reactor arrangements, are processed to achieve desired degrees of separation and/or other processing.
- the effluent will generally also include HC1, unreacted HF, and trace amounts, if any, of unreacted starting component (e.g. 1230xa, 1230xf and/or 240db).
- the effluent may also include one or more by-product organics such as
- underfluorinated and/or overfluorinated intermediates include underfluorinated and/or overfluorinated intermediates.
- underfhiorinated intermediates include trichlorofluoropropene (1231) isomers and 2,3- dichloro-3,3-difluoropropene (1232xf), and non-limiting examples of overfluorinated intermediates include 2-chloro-l,l,l,2-tetrafluoropropane (244bb) and 1,1,1,2,2- pentafluoropropane (245cb).
- Other by-product organics may also include, but are not limited to, dichlorotrifluoropropane (243), and trichlorodifluoropropane (242).
- reaction by-products include one or more of
- dichlorotrifluoropropanes include, but are not limited to, one or more of the compounds 2,2- dichloro-l,l,l-trifluoropropane (HCFC-243ab), 2,3-dichloro-l,l,l-trifluoropropane (HCFC- 243db), and l,2-dichloro-l,l,2-trifluoropropane (HCFC-243bc).
- Trichlorodifluoropropanes include, but are not limited to, one or more of the compounds l,2,2-trichloro-l,l- difluoropropane (HCFC-242ac), l,l,2-trichloro-l,2-difluoropropane (HCFC-242bc), and 1 ,2,3-trichloro- 1 , 1 -difluoropropane (HCFC-242dc) .
- the effluent may be processed in one or more steps to isolate the 1233xf, as well as certain unreacted components and/or byproducts that are useful as a recyclables (including, but not limited to, the 242 and 243 isomers).
- Such isolation steps include those known in the art, and include without limitation, those described in US Patent Nos. 8258355 and 8084653 the entire contents of which are incorporated herein by reference.
- a first recycle column such as a distillation column is provided.
- the lighter components of the effluent are isolated from the top of the first recycle column and cooled and include one or more of HC1, 1233xf, 244bb (if any), 245cb (if any) and a portion of unreacted HF.
- the remaining compounds are collected at the bottom stream of the column and include a bulk of the unreacted HF, trace amounts of unreacted starting component (if any), residual 1233xf and one or more of the by-product organics discussed herein.
- a "residual" amount of 1233xf refers to less than about 30 wt %, less than about 20%, less than about 15%, or less than about 10% of the total weight of the components in the bottom stream.
- top stream and bottom stream are then independently processed.
- the top stream for example, is first fed into an HC1 column for HC1 removal.
- High purity HC1 is isolated from the top of the column and fed to an HC1 recovery system.
- HC1 from the top stream may be absorbed in de- ionized water as concentrated HC1 which, optionally, can be recovered for later sale.
- the remaining components including 1233xf, 244bb (if any), 245cb (if any), and HF, exit the bottom of the HC1 column and are further processed.
- this bottom stream is then provided to an HF recovery system to recover HF.
- the 1233xf/HF stream is fed to a sulfuric acid extractor or a phase separator for removal of HF from this mixture, i.e. the HF is either dissolved in sulfuric acid or phase separated from the organic mixture.
- a sulfuric acid extractor or a phase separator for removal of HF from this mixture, i.e. the HF is either dissolved in sulfuric acid or phase separated from the organic mixture.
- HF is desorbed from the sulfuric acid/HF mixture by heating and distillation and recycled back to the reactor.
- HF is phase- separated using standard methods, such as those discussed below, and recycled back to the reactor.
- the organic either from the overhead of the sulfuric acid extractor or from the bottom layer of the phase separator is fed to the hydrofluorination reactor of Step (2), discussed below.
- phase separation Components within the bottom stream of the first recycle column are separated, in certain embodiments, by phase separation. More specifically, the mixture is provided to a cooler and then to a phase separator where unreacted HF separates into an HF-rich first or top layer and an organic rich bottom or second layer. Any pressure which maintains the mixture substantially in the liquid phase may be employed. To this end, the pressure and temperature of the mixture may be adjusted such that the mixture remains substantially in the liquid phase.
- the HF-rich layer also includes, as a residual portion, certain of the organics such as, but not limited to 1233xf, 1232xf and 243.
- phase separation may be performed at any combination of temperature and pressure such that two distinct liquid phases are formed in the phase separator. Phase separation may be carried out between about -30°C to 60°C, preferably between about 0°C and 40 °C and more preferably between about 10°C and 30°C.
- the HF rich layer is then isolated, such as by an HF phase pump, optionally purified, and recycled back to the reactor via a vaporizer.
- the HF-rich layer is distilled to remove any moisture buildup or is isolated by single stage flash distillation.
- moisture if any is removed by injecting a chemical reagent such as COCl 2 (or SOCl 2 ) into said stream, which reacts with moisture to form C0 2 (or S0 2 ) and HCl.
- the HF-rich layer may be purified to remove the residual organics or may be recycled with the organics.
- the organic -rich layer is also isolated, such as by an organic phase pump, then further processed to separate and purify the unreacted starting reactants (if any) and recyclable intermediates or by-products.
- the organic-rich layer is provided to a high boiler purge system, where unreacted starting reagents (if any), residual 1233xf, 1231 isomers, 1232xf, 243 isomers, 242 isomers, etc. are recovered and undesirable by-products are removed.
- a "residual" amount of HF refers to less than about 15 wt %, less than about 10%, less than about 5%, or less that about 3% of the total weight of the components in the bottom layer.
- the high boiler purge system may be a distillation system operated in batch or continuous mode, preferably batch for operational reasons. Another option is to use a flash or series of flashes. In either case (distillation or flash), the more volatile components are recovered and recycled while the heavier components are removed from the system.
- the purified 1233xf intermediate stream is converted to 2-chloro-l,l,l,2-tetrafluoropropane (244bb).
- this step may be performed in the liquid phase in a liquid phase reactor, which may be TFE or PFA-lined. Such a process may be performed in a temperature range of about 70-120 °C and about 50-120 psig.
- liquid phase fluorination catalyst may be used in the invention.
- a non-exhaustive list include Lewis acids, transition metal halides, transition metal oxides, Group IVb metal halides, Group Vb metal halides, or combinations thereof.
- Non-exclusive examples of liquid phase fluorination catalysts are an antimony halide, a tin halide, a tantalum halide, a titanium halide, a niobium halide, and molybdenum halide, an iron halide, a fluorinated chrome halide, a fluorinated chrome oxide or combinations thereof.
- liquid phase fluorination catalysts are SbCl 5 , SbCl 3 , SbF 5 , SnCl 4 , TaCl 5 , TiCl 4 , NbCl 5 , MoCl 6 , FeCl 3 , a fluorinated species of SbCl 5 , a fluorinated species of SbCl 3 , a fluorinated species of SnCl 4 , a fluorinated species of TaCl 5 , a fluorinated species of TiCl 4 , a fluorinated species of NbCl 5 , a fluorinated species of Mode, a fluorinated species of FeCl 3 , or combinations thereof.
- Antimony pentachloride is most preferred.
- These catalysts can be readily regenerated by any means known in the art if they become deactivated.
- One suitable method of regenerating the catalyst involves flowing a stream of chlorine through the catalyst. For example, from about 0.002 to about 0.2 lb per hour of chlorine can be added to the liquid phase reaction for every pound of liquid phase fluorination catalyst. This may be done, for example, for from about 1 to about 2 hours or continuously at a temperature of from about 65 °C to about 100 °C.
- This second step of the reaction is not necessarily limited to a liquid phase reaction and may also be performed using a vapor phase reaction or a combination of liquid and vapor phases, such as that disclosed in U.S. Published Patent Application No. 20070197842, the contents of which are incorporated herein by reference.
- the 1233xf containing feed stream is preheated to a temperature of from about 50 °C to about 400 °C, and is contacted with a catalyst and fluorinating agent.
- Catalysts may include standard vapor phase agents used for such a reaction and fluorinating agents may include those generally known in the art, such as, but not limited to, hydrogen fluoride.
- 243ab may be formed in varying degrees as a by-product. This is often particularly the case when a chloride such as HC1 is a co-feed to this reaction. The unwanted generation of 243ab comes at the expense of 244bb yield.
- the 243ab thus formed is converted to 1233xf by catalytic dehydrochlorination. The 1233xf obtained by this conversion can be recycled back to the second step of the reaction or used for other purposes.
- the 243ab is separately converted to recyclable 1233xf, subject to removal of 243ab from the product mixture of the second step of the reaction, as known in the art.
- the 243ab is sent to the third step of the reaction, discussed hereunder, whereby it is dehydrochlorinated to form 1233xf as part of the process to dehydrochlorinate 244bb to 1234yf.
- the same reactor, catalysts, and conditions may be employed.
- the 1233xf thus obtained can be separated to the extent necessary as known in the art, and can be recycled back to the second step of the reaction whereby 244bb is generated, or it can be used otherwise.
- the 244bb is fed to a second vapor phase reactor (dehydrochlorination reactor) to be dehydrochlorinated to make the desired product 2,3,3,3-tetrafluoroprop-l-ene (1234yf).
- This reactor contains a catalyst that can catalytically dehydrochlorinate HCFC-244bb to make HFO-1234yf.
- the 244bb that is fed to the third step of 1234yf production process further comprises all or part of the 243ab that may have formed in the second step of the reaction.
- the reactor and catalyst suitable for dehydrochlorinating 244bb to 1234yf in this third step can also act to dehydrochlorinate 243ab to 1233xf, which can be optionally reused via recycle.
- the catalysts may be metal halides, halogenated metal oxides, neutral (or zero oxidation state) metal or metal alloy, or activated carbon in bulk or supported form.
- Metal halide or metal oxide catalysts may include, but are not limited to, mono-, bi-, and tri-valent metal halides, oxides and their mixtures/combinations, and more preferably mono-, and bivalent metal halides and their mixtures/combinations.
- Component metals include, but are not limited to, Cr 3+ , Fe 3+ , Mg 2+ , Ca 2+ , Ni 2+ , Zn 2+ , Pd 2+ , Li + , Na + , K + , and Cs + .
- Component halogens include, but are not limited to, F “ , CI “ , Br “ , and ⁇ .
- useful mono- or bivalent metal halide include, but are not limited to, LiF, NaF, KF, CsF, MgF 2 , CaF 2 , LiCl, NaCl, KCl, and CsCl.
- Halogenation treatments can include any of those known in the prior art, particularly those that employ HF, F 2 , HCl, Cl 2 , HBr, Br 2 , HI, and I 2 as the halogenation source.
- metals, metal alloys and their mixtures are used.
- Useful metals include, but are not limited to, Pd, Pt, Rh, Fe, Co, Ni, Cu, Mo, Cr, Mn, and combinations of the foregoing as alloys or mixtures.
- the catalyst may be supported or unsupported.
- Useful examples of metal alloys include, but are not limited to, SS 316, Monel 400, Inconel 825, Inconel 600, and Inconel 625. Such catalysts may be provided as discrete supported or unsupported elements and/or as part of the reactor and/or the reactor walls.
- Preferred, but non-limiting, catalysts include activated carbon, stainless steel (e.g. SS 316), austenitic nickel-based alloys (e.g. Inconel 625), nickel, fluorinated 10% CsCl/MgO, and 10% CsCl/MgF 2 .
- the reaction temperature is preferably about 300-550 °C and the reaction pressure may be between about 0-150 psig.
- the reactor effluent may be fed to a caustic scrubber or to a distillation column to remove the by-product of HCl to produce an acid-free organic product which, optionally, may undergo further purification using one or any combination of purification techniques that are known in the art.
- the aforementioned catalysts for dehydrochlorination of 244bb to 1234yf are also useful for dehydrochlorination of 243ab to 1233xf, including in practices where this latter dehydrochlorination occurs in the third step of the reaction, as preferred, or is separately performed.
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Abstract
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Priority Applications (5)
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MX2015010962A MX2015010962A (en) | 2013-03-15 | 2014-03-13 | Process for producing 2,3,3,3-tetrafluoropropene. |
KR1020157028060A KR20150130414A (en) | 2013-03-15 | 2014-03-13 | Process for producing 2,3,3,3-tetrafluoropropene |
JP2016501952A JP6420816B2 (en) | 2013-03-15 | 2014-03-13 | Method for producing 2,3,3,3-tetrafluoropropene |
EP14767400.6A EP2970053A4 (en) | 2013-03-15 | 2014-03-13 | Process for producing 2,3,3,3-tetrafluoropropene |
CN201480016017.4A CN105189420A (en) | 2013-03-15 | 2014-03-13 | Process for producing 2,3,3,3-tetrafluoropropene |
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US201361792769P | 2013-03-15 | 2013-03-15 | |
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PCT/US2014/025733 WO2014151441A1 (en) | 2013-03-15 | 2014-03-13 | Process for producing 2,3,3,3-tetrafluoropropene |
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US (3) | US20140275651A1 (en) |
EP (1) | EP2970053A4 (en) |
JP (2) | JP6420816B2 (en) |
KR (1) | KR20150130414A (en) |
CN (1) | CN105189420A (en) |
MX (1) | MX2015010962A (en) |
WO (1) | WO2014151441A1 (en) |
Cited By (1)
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US10301236B2 (en) | 2015-05-21 | 2019-05-28 | The Chemours Company Fc, Llc | Hydrofluorination of a halogenated olefin with SbF5 in the liquid phase |
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GB2559056B (en) | 2015-07-17 | 2019-09-11 | Mexichem Fluor Sa De Cv | Process for preparing 245cb and 1234yf from 243db |
KR101992230B1 (en) * | 2017-08-08 | 2019-06-25 | (주)후성 | Process for simultaneous production of 1,1,1-trifluoro-2chloropropene and 1,1,1,2-tetrafluoropropene using gas phase catalyst |
WO2020014130A1 (en) * | 2018-07-09 | 2020-01-16 | The Chemours Company Fc, Llc | Compositions and methods for an integrated 2,3,3,3-tetrafluoropropene manufacturing process |
EP3847145A2 (en) * | 2018-09-07 | 2021-07-14 | The Chemours Company FC, LLC | Fluorine removal from antimony fluorohalide catalyst using chlorocarbons |
AU2020287313A1 (en) * | 2019-06-04 | 2021-12-02 | The Chemours Company Fc, Llc | 2-chloro-3,3,3-trifluoropropene (1233XF) compositions and methods for making and using the compositions |
CN112778079A (en) * | 2019-11-05 | 2021-05-11 | 浙江环新氟材料股份有限公司 | Process for producing 2-chloro-1, 1, 1, 2-tetrafluoropropane and 2, 3, 3, 3-tetrafluoropropene |
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Cited By (5)
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US10301236B2 (en) | 2015-05-21 | 2019-05-28 | The Chemours Company Fc, Llc | Hydrofluorination of a halogenated olefin with SbF5 in the liquid phase |
US10988422B2 (en) | 2015-05-21 | 2021-04-27 | The Chemours Company Fc, Llc | Hydrofluoroalkane composition |
US11008267B2 (en) | 2015-05-21 | 2021-05-18 | The Chemours Company Fc, Llc | Hydrofluoroalkane composition |
US11572326B2 (en) | 2015-05-21 | 2023-02-07 | The Chemours Company Fc, Llc | Method for preparing 1,1,1,2,2-pentafluoropropane |
US12006274B2 (en) | 2015-05-21 | 2024-06-11 | The Chemours Company Fc, Llc | Compositions including olefin and hydrofluoroalkane |
Also Published As
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US20160304420A1 (en) | 2016-10-20 |
US20140275651A1 (en) | 2014-09-18 |
JP6420816B2 (en) | 2018-11-07 |
EP2970053A1 (en) | 2016-01-20 |
KR20150130414A (en) | 2015-11-23 |
CN105189420A (en) | 2015-12-23 |
US9701599B2 (en) | 2017-07-11 |
MX2015010962A (en) | 2015-12-17 |
EP2970053A4 (en) | 2016-11-02 |
JP2016511287A (en) | 2016-04-14 |
US20170283348A1 (en) | 2017-10-05 |
JP2019055951A (en) | 2019-04-11 |
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