EP3099655A1 - Process for the manufacture of hydrochlorofluoroolefins - Google Patents

Process for the manufacture of hydrochlorofluoroolefins

Info

Publication number
EP3099655A1
EP3099655A1 EP15743421.8A EP15743421A EP3099655A1 EP 3099655 A1 EP3099655 A1 EP 3099655A1 EP 15743421 A EP15743421 A EP 15743421A EP 3099655 A1 EP3099655 A1 EP 3099655A1
Authority
EP
European Patent Office
Prior art keywords
catalyst
trans
cis
liquid phase
isomerization
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.)
Withdrawn
Application number
EP15743421.8A
Other languages
German (de)
French (fr)
Other versions
EP3099655A4 (en
Inventor
Maher Y. Elsheikh
Philippe Bonnet
John A. Wismer
Sri R. Seshadri
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Arkema Inc
Original Assignee
Arkema Inc
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
Priority claimed from US14/167,150 external-priority patent/US8987534B2/en
Application filed by Arkema Inc filed Critical Arkema Inc
Publication of EP3099655A1 publication Critical patent/EP3099655A1/en
Publication of EP3099655A4 publication Critical patent/EP3099655A4/en
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00—Preparation of halogenated hydrocarbons
    • C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
    • C07C17/358—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction by isomerisation
    • 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
    • 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 a process for the manufacture of
  • CFCs chlorofluorocarbons
  • HFCs hydrofluorocarbons
  • ODP negligible ozone depletion potential
  • GWP acceptable low global warming potential
  • the present invention describes a process for manufacturing of the hydrochlorofluoroolefin, trans 1233zd (E- 1233zd, l-chloro-3,3,3-trifluorpropene) which is useful as a low ODP and low GWP blowing agent for thermoset and thermoplastic foams, solvent, heat transfer fluid such as in heat pumps, and refrigerant such as a low pressure refrigerant for chillers.
  • US patent publications US2008/0051610 and US2008/0103342 disclose a process that includes a step of the catalytic isomerization of cis 1234ze to trans 1234ze.
  • 7,420,094 discloses the isomerization of 1234ze to 1234yf with a Cr based catalyst.
  • US2008/0051611 discloses the recovery of trans 1234ze from a mixture that includes cis 1234ze and trans 1234ze via distillation.
  • hydrochlorofluoroolefin, trans l-chloro-3,3,3-trifluoropropene (E-1233zd).
  • the process comprises an isomerization step from cis 1233zd (Z-1233zd) to trans 1233zd (E- 1233zd).
  • Figure 1 is a schematic of a liquid phase process in accordance with the present invention.
  • Figure 2 is schematic of a gas phase process in accordance with the present invention.
  • Figure 3 is schematic of a liquid phase process including recycle of 1233zd in accordance with the present invention.
  • Figure 4 is schematic of a gas phase process including recycle of 1233zd in accordance with the present invention.
  • the present invention provides a process for the manufacture of trans l-chloro-3,3,3- trifluoropropene (E-1233zd).
  • the second step of the process comprises a separation of the mixture formed in the first step to isolate cis 1233zd (Z-1233zd) from the mixture.
  • the third step of the process comprises isomerization of cis 1233zd (Z-1233zd) to trans 1233zd (E- 1233zd).
  • VCM vinyl chloride monomer
  • the present invention is directed toward a process for producing trans l-chloro-3,3,3- trifluoro propene (E-1233zd) from 1,1,3,3 -tetrachlororopropene (1230za),
  • the first step of the process gas phase fluorination of 1230za and/or 240fa to 1233zd or liquid phase fluorination of 1230za to 12333zd; can be via any process known in the art.
  • the uncatalyzed liquid phase fluorination of 1230za is disclosed in US Patent No. 5,877,359; the catalyzed gas phase fluorination of 1230za is disclosed in US Patent No. 5,811,603; US Patent No. 6,166,274 discloses the fluorination of 1230za to 1233zd in the presence of catalyst such as trifluoroacetic acid or triflic acid.
  • Sb type catalyst it is preferred to feed low level of Cl 2 to maintain the Sb species in an active form.
  • the second step of the process comprises the separation of the cis 1233zd and trans 1233zd formed in the first step via an appropriate separation means such as distillation, liquid phase separation, or extractive separation.
  • the cis 1233zd and trans 1233zd formed in the first step may contain HF and HCl.
  • the HCl is first removed in a first distillation column.
  • liquid phase separation coupled with azeotropic distillation can be used to remove HF.
  • the boiling point difference of cis 1233zd and trans 1233zd enable them to be separated by
  • the third step of the process involves the isomerization of the cis 1233zd from the second step into trans 1233zd.
  • the isomerization step can be carried out in the gas phase or in the liquid phase using respectively a heterogeneous or a homogeneous catalyst.
  • the isomerization step is achievable with a gas phase process in the presence of a heterogeneous catalyst.
  • a suitable heterogeneous catalyst is high surface area Cr (III) catalyst, supported or unsupported, that can optionally contains low levels of one or more co-catalysts selected from cobalt, nickel, zinc or manganese.
  • the catalyst support can be selected from materials known in the art to be compatible with high temperature and pressure processes.
  • fluorinated alumina, HF treated activated carbon or carbon graphite are suitable catalyst supports.
  • a preferred catalyst is a high surface area unsupported chromium oxide catalyst that is activated with HF before use, optionally at pressure above 50 psi.
  • the level of the co-catalyst when present, can be varied from 1 to 10 weight , preferably from 1 to 5 weight % of the catalyst.
  • Co-catalyst can be added to the catalyst by processes known in the art such as adsorption from an aqueous or organic solvent, followed by solvent evaporation.
  • Suitable heterogeneous catalyst can also be selected from: Lewis acids supported catalysts selected from Sb v , Ti w , Sn IV , Mo VI , Nb v and Ta v'
  • the support itself is selected from the group such as fluorinated alumina; fluorinated chromia; HF activated carbon or graphite carbon .
  • Supported antimony halides such as SbF 5 are described in US Patent No. 6,528,691 and are preferred catalysts.
  • Other solid catalysts such as NAFION ® type polymer, acidic molecular sieves and, zeolites can be also used.
  • the temperature can be varied between 20-500°C, preferably between 100-400°C.
  • Contact times can vary from 0.5 to 100 seconds.
  • a low level of oxidizing agent such as oxygen or oxygen containing gas such as air or chlorine gas can be used at between .01- .1 volume percent to prolong the life of the catalyst.
  • the isomerization step is also achievable in a liquid phase process in the presence of a homogenous catalyst preferably selected from compounds of group 3, 4, 5, 13, 14 and 15 metal compounds of the Periodic Table of the elements (IUPAC 1988) and their mixtures (groups of the Periodic Table of the elements which were previously called IIIA, IVa, IVb, Va, Vb and VIb).
  • a homogenous catalyst preferably selected from compounds of group 3, 4, 5, 13, 14 and 15 metal compounds of the Periodic Table of the elements (IUPAC 1988) and their mixtures (groups of the Periodic Table of the elements which were previously called IIIA, IVa, IVb, Va, Vb and VIb).
  • the compounds of the metals are intended to include hydroxides, oxides and the organic or inorganic salts of these metals, as well as mixtures thereof.
  • the aluminum, titanium, tantalum, molybdenum, boron, tin and antimony derivatives such as A1C1 3 , TiCl 4 , TaCl 5 , Mod , BF 3 , SnCl 4 , and SbC15.
  • the catalyst must be subjected to activation (by HF or any molecule able to exchange fluorine) prior to the isomerization step.
  • activation by HF or any molecule able to exchange fluorine
  • a low level of chlorine gas as oxidizing agent can be used to maintain the antimony catalyst in the pentavalent oxidation state.
  • an ionic liquid derived from antimony, titanium, niobium and tantalum is suitable for liquid phase fluorination processes. A description of the preparation of such catalysts is disclosed in the US Patent No. 6,881,698.
  • the homogenous catalyst for a liquid phase process can also be selected from the Bronsted type family of acids such as (but not limited to) sulfuric acid H 2 S0 4 , sulfonic type acids such as CISO 3 H or FSO 3 H or triflic acid CF 3 SO 3 H or methane sulfonic acid CH 3 SO 3 H.
  • the operating temperature can be varied between about 20-200°C, with a contact time between about 0.5-50 hours
  • Isomerization can also be accomplished, in the primary 1233zd reactors- either in the gas or liquid phase. This allows the separated Z-1233zd to be recycled back to the primary reactors and avoids the need for separate isomerization reactors, RI-1 and RI- 2. See figures 3 and 4. It is believed this recycle would result in the Z-1233zd levels building to an equilibrium limit, after which the Z-1233zd would isomerizes in RFL-1 or RFG-2 at the same rate that it was being formed.
  • the process of the present invention may comprise additional separation steps between each step.
  • the purpose of theses separations could be:
  • RFL- comprises a liquid phase fluorination reactor and rectification system comprising an unagitated, jacketed pressure vessel connected to a rectification column.
  • the reactor also acts as the reboiler of the rectification column.
  • the HF and organic (1230za) are fed directly to the reactor.
  • the molar feed ratio of HF to organic is dictated by the reaction stoichiometry and the amount of HF leaving the reactor with the rectification column overhead and liquid phase purges. Mixing is provided by the boiling action of the reactor contents.
  • the reactor effluent leaves the reactor vessel as a gas and enters the bottom of the rectification column.
  • a small purge from the liquid phase can remove any non-volatiles that may form during the reaction.
  • the rectification column contains either packing or trays designed to provide good mass transfer between up flowing gas and down flowing liquid.
  • the condenser at the top of the column is cooled by either cooling water, chilled water, or some type of refrigeration.
  • the condenser is a partial condenser where the liquid effluent is refluxed directly back to the column.
  • the vapor effluent consists of HCl, HF and organic components.
  • DH- comprises an HCl distillation system whereby pure HCl is removed from the top of a distillation column.
  • This column can operate between 100 psig and 300 psig. More typically, the HCl is distilled above 120 psig to allow the use of conventional (- 40C) refrigeration at the top of the HCl column.
  • the bottoms of this column contains HF and organic with a small residual amount of HCl. The ratio of HF to the organic component typically is close to the azeotropic composition.
  • PS- comprises a liquid phase separator to separate two liquid phases, one consisting primarily of a hydrochlorofluorocarbon (HCFC) and the other consisting primarily of HF.
  • HCFC hydrochlorofluorocarbon
  • the HF phase is usually the less dense so that it exits from the top of the phase separator and the HCFC exits as the bottom phase.
  • the operating temperature of the phase separator can be between -40°C and +20°C. However, the lower the temperature, the better the phase separation.
  • DA- comprises an azeotropic distillation column which distills overhead an azeotropic composition of HF and an organic consisting of one or more HCFC's
  • the bottoms composition is either entirely HF or entirely organic, depending on whether the column feed composition is on the HF rich side or the organic rich side of the azeotrope. If the bottoms are HF, this stream is normally recycled back to the reactor. If the bottoms steam is organic, it is sent to a conventional distillation train.
  • DS- comprises a straight distillation normally done under pressure.
  • the module consists of a feed vaporizer and superheater. It can include an "economizer", whereby hot effluent is fed to one side and relatively cold reactor feed gases are fed to another side of a heat exchanger. The effluent gases are further cooled before entering a distillation column. Isomerization reactions can be run at varying conversions depending on the equilibrium distribution of isomers.
  • the effluent isomers can have boiling points very close together. However, they typically exhibit close to ideal behavior so can be separated by conventional distillation.
  • this reaction can be done as a homogeneously catalyzed liquid phase reaction. In this
  • the reactor would be a continuous stirred tank with the effluent being removed as a vapor to effect separation from the catalyst.
  • RFG- comprises a gas phase fluorination reactor that is an adiabatic packed bed reactor that feeds a gas phase over a solid catalyst. No cooling is needed because of the reactor has a low conversion per pass and a high HF molar feed ratio.
  • the adiabatic exotherm is typically less than 100°C.
  • the feed HF and organic are vaporized in a common vaporizer and superheated to the reactor temperature.
  • the common vaporizer allows the 1230za and/or 240fa to be vaporized at a lower temperature than would be possible if it were vaporized as a pure component, thereby minimizing thermal degradation.
  • This module can also include an "economizer", whereby hot effluent is fed to one side and relatively cold reactor feed gases are fed to another side of a heat exchanger. The effluent gases are further cooled before entering a distillation column. Reaction temperatures are between 200°C and 400°C. The pressure is high enough to allow the HC1 by-product to be distilled with conventional refrigeration- preferably between 100 psig and 200 psig.
  • the lower case letter used to identify the modules distinguishes multiple appearances of the same type of module in the same process.
  • Figure 1 is a block flow diagram of a process in accordance with the present invention for converting 1230za to E-1233zd using a liquid phase fluorination step.
  • the Figure incorporates the process modules described above.
  • Figure 1 discloses a process wherein 1230za and HF are fed to reaction module RFL-1. Typically, the reaction takes place in a predominantly HF rich medium without a catalyst.
  • the HC1 and the 1233zd/HF exit the top of the rectification column of RFL-1.
  • the vapor effluent of RFL-1 enters DH-1 to remove HC1 as a pure overhead product.
  • the bottoms of DH-1 consists primarily of 1233zd (both E and Z isomers) and HF at a near azeotropic composition.
  • module PS- 1 This is fed to module PS- 1 to effect a liquid phase separation.
  • the top HF rich phase is sent to module DA- la, where HF is separated as a bottoms stream for recycle to the reactor.
  • the overhead azeotrope of 1233zd and HF is recycled back to DH-1 to allow any residual HC1 and light organics to be stripped out in this column before the azeotrope gets recycled to phase separation.
  • the bottoms stream from PS- 1 goes to module DA- lb, which removes an organic stream devoid of HF as a bottoms stream.
  • the overhead from DA- lb is recycled to DH-1 for the same reason that the DA- la azeotrope was recycled to DH-1.
  • DA- lb The bottoms of DA- lb is sent to process module DS-1 that separates any heavies from the 1233zd.
  • the overhead from DS-1 is E-1233zd, the desired trans isomer.
  • the Z-1233zd is higher boiling and is recovered for feeding to process module RI-1.
  • the effluent from the isomerization reactor is recycled to DS-1, which effects the separation of the E and Z isomers.
  • FIG. 2 is a block flow diagram of a process in accordance with the present invention for converting 1230za or 240fa to E-1233zd using a gas phase fluorination step.
  • the Figure incorporates the process modules described above.
  • the process is similar to Figure 1 except, for example, the liquid phase fluorination reactor (RFL-1) is replaced by a gas phase fluorination reactor (RFG-1) and azeotropic distillation column (DA-2a).
  • the process as outlined by Figure 2 comprises feeding 1230za and/or 240fa and HF to reaction module RFG-2.
  • the reaction takes place in a gas phase with a catalyst.
  • the reactor effluent consists of predominantly HC1, 1233zd, unreacted 1230za and excess HF.
  • the reactor effluent of RFG-2 enters DA-2a to remove HF and unreacted F1230za as bottoms that is recycled to the reactor.
  • the overhead which consists predominantly of HC1 and the azeotrope of HF and 1233zd (both E and Z isomers), is sent to DH-2, which removes HC1 as a pure overhead product.
  • the bottoms of DH-2 consists of primarily 1233zd (both E and Z isomers) and HF at a near azeotropic composition. This is fed to module PS-2 to effect a liquid phase separation.
  • the top HF rich phase is sent to module DA-2b, where HF is separated as a bottoms stream for recycle to the reactor.
  • the overhead azeotrope of 1233zd and HF is recycled back to DH-2 to allow any residual HC1 and light organic s to be stripped out in this column before the azeotrope gets recycled to phase separation.
  • the bottoms stream from PS- 2 goes to module DA-2c, which removes an organic stream devoid of HF as a bottoms stream.
  • the overhead from DA-2c is recycled to DH-2 for the same reason that the DA-2b azeotrope was recycled to DH-2.
  • the bottoms of DA-2c is sent to process module DS-2 that separates any heavies from the 1233zd.
  • the overhead from DS-2 is E-1233zd- the desired trans isomer.
  • the Z-1233zd is higher boiling and is recovered for feeding to process module RI-2.
  • the effluent from the isomerization reactor is recycled to DS-2, which effects the separation of the E and Z isomers.
  • Z-1233zd could be recycled directly to RFG-2 as shown in Figure 4, where isomerization could occur so as to limit the Z-1233zd concentration in RFG-2 to an equilibrium level.

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  • 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)

Abstract

The disclosure provides a process for the manufacture of trans 1-chloro3,3,3-trifluoropropene (trans 1233zd) by fluorinating 1230za and/or 240fa to a cis/trans mixture of 1233zd, separating the trans isomer followed by an isomerization of cis 1233zd to trans 1233zd in the fluorination step. The fluorination step is carried out in the gas phase or the liquid phase. The isomerization is carried out in the gas phase with a high surface area heterogeneous Cr catalyst, supported or unsupported.

Description

PROCESS FOR THE MANUFACTURE OF
HYDROCHLOROFLUOROOLEFINS
Field of The Invention
The present invention relates to a process for the manufacture of
hydrochlorofluoroolefins.
Background of the Invention
The Montreal Protocol for the protection of the ozone layer mandates the phase out of the use of chlorofluorocarbons (CFCs). Materials more "friendly" to the ozone layer such as hydrofluorocarbons (HFCs) e.g. 134a replaced chlorofluorocarbons. The latter compounds have proven to be greenhouse gases, causing global warming and could be regulated by the Kyoto Protocol on Climate Change. Replacement materials are needed which are environmentally acceptable i.e. have negligible ozone depletion potential (ODP) and acceptable low global warming potential (GWP). The present invention describes a process for manufacturing of the hydrochlorofluoroolefin, trans 1233zd (E- 1233zd, l-chloro-3,3,3-trifluorpropene) which is useful as a low ODP and low GWP blowing agent for thermoset and thermoplastic foams, solvent, heat transfer fluid such as in heat pumps, and refrigerant such as a low pressure refrigerant for chillers.
US patent publications US2008/0051610 and US2008/0103342 disclose a process that includes a step of the catalytic isomerization of cis 1234ze to trans 1234ze. US
7,420,094 discloses the isomerization of 1234ze to 1234yf with a Cr based catalyst. US2008/0051611 discloses the recovery of trans 1234ze from a mixture that includes cis 1234ze and trans 1234ze via distillation.
Summary of the Invention The present invention relates a process for the manufacture of the
hydrochlorofluoroolefin, trans l-chloro-3,3,3-trifluoropropene (E-1233zd). The process comprises an isomerization step from cis 1233zd (Z-1233zd) to trans 1233zd (E- 1233zd). Brief Summary of the Drawings
Figure 1 is a schematic of a liquid phase process in accordance with the present invention.
Figure 2 is schematic of a gas phase process in accordance with the present invention.
Figure 3 is schematic of a liquid phase process including recycle of 1233zd in accordance with the present invention.
Figure 4 is schematic of a gas phase process including recycle of 1233zd in accordance with the present invention.
Detailed Description of the Invention
The present invention provides a process for the manufacture of trans l-chloro-3,3,3- trifluoropropene (E-1233zd). The first step of the process comprises the fluorination of 1,1,3,3- tetrachlororopropene (1230za, CC12=CH-CHC12) and/or 1,1,1,3,3- pentaachloropropane (240fa) to a mixture of cis 1233zd (Z-1233zd) and trans 1233zd (E- 1233zd). The second step of the process comprises a separation of the mixture formed in the first step to isolate cis 1233zd (Z-1233zd) from the mixture. The third step of the process comprises isomerization of cis 1233zd (Z-1233zd) to trans 1233zd (E- 1233zd).
The 1230za used in the first step can be obtained by the reaction of CC14 and vinyl chloride monomer (VCM, CH2=CHC1) to form 1,1,1,3,3 -pentachloropropane (240fa) which can be dehydrochlorinated to produce 1230za.
The present invention is directed toward a process for producing trans l-chloro-3,3,3- trifluoro propene (E-1233zd) from 1,1,3,3 -tetrachlororopropene (1230za),
(CC12=CH-CHC12) and/ or 1,1,1,3,3-tetrachloropropane (240fa) that comprises the steps of: a) fluorination of 1,1,3,3- tetrachlororopropene (1230za, CC12=CH-CHC12) and/or 1,1,1,3,3-pentachoropropane (240fa) in gas phase, or liquid phase fluorination of 1230za to obtain a mixture of cis (Z) and trans (E) 1- chloro-3,3,3 trifluoro propene (1233zd, CF3-CH=CHC1); followed by b) separation of cis (Z) 1-chloro 3,3,3-trifhioropropene (1233zd, CF - CH=CHC1) and trans (E) 1-chloro 3,3,3-trifluoropropene (1233zd, CF3- CH=CHC1); followed by c) isomerization of the cis 1233zd (Z- 1233zd) from the second step to form trans 1233zd (E-1233zd).
The first step of the process, gas phase fluorination of 1230za and/or 240fa to 1233zd or liquid phase fluorination of 1230za to 12333zd; can be via any process known in the art. For example: the uncatalyzed liquid phase fluorination of 1230za is disclosed in US Patent No. 5,877,359; the catalyzed gas phase fluorination of 1230za is disclosed in US Patent No. 5,811,603; US Patent No. 6,166,274 discloses the fluorination of 1230za to 1233zd in the presence of catalyst such as trifluoroacetic acid or triflic acid. Fluorination catalysts such as TiCl4, TiF4, SnCl4, SnF4, SbFs, SbCls, SbFxCly (x+y=5), or an ionic liquid are described in US Patent No. 6,881,698. When an Sb type catalyst is used, it is preferred to feed low level of Cl2 to maintain the Sb species in an active form.
The second step of the process comprises the separation of the cis 1233zd and trans 1233zd formed in the first step via an appropriate separation means such as distillation, liquid phase separation, or extractive separation. The cis 1233zd and trans 1233zd formed in the first step may contain HF and HCl. Preferably, the HCl is first removed in a first distillation column. Thereafter, liquid phase separation coupled with azeotropic distillation can be used to remove HF. The boiling point difference of cis 1233zd and trans 1233zd enable them to be separated by
conventional distillation, typically at atmospheric pressures.
The third step of the process involves the isomerization of the cis 1233zd from the second step into trans 1233zd. The isomerization step can be carried out in the gas phase or in the liquid phase using respectively a heterogeneous or a homogeneous catalyst.
The isomerization step is achievable with a gas phase process in the presence of a heterogeneous catalyst. A suitable heterogeneous catalyst is high surface area Cr(III) catalyst, supported or unsupported, that can optionally contains low levels of one or more co-catalysts selected from cobalt, nickel, zinc or manganese. For supported catalyst, the catalyst support can be selected from materials known in the art to be compatible with high temperature and pressure processes. For example, fluorinated alumina, HF treated activated carbon or carbon graphite are suitable catalyst supports. A preferred catalyst is a high surface area unsupported chromium oxide catalyst that is activated with HF before use, optionally at pressure above 50 psi. The level of the co-catalyst, when present, can be varied from 1 to 10 weight , preferably from 1 to 5 weight % of the catalyst. Co-catalyst can be added to the catalyst by processes known in the art such as adsorption from an aqueous or organic solvent, followed by solvent evaporation. Suitable heterogeneous catalyst can also be selected from: Lewis acids supported catalysts selected from Sbv, Tiw, SnIV, MoVI, Nbv and Tav' The support itself is selected from the group such as fluorinated alumina; fluorinated chromia; HF activated carbon or graphite carbon . Supported antimony halides such as SbF5 are described in US Patent No. 6,528,691 and are preferred catalysts. Other solid catalysts such as NAFION® type polymer, acidic molecular sieves and, zeolites can be also used.
For the gas phase process, the temperature can be varied between 20-500°C, preferably between 100-400°C. Contact times can vary from 0.5 to 100 seconds. A low level of oxidizing agent such as oxygen or oxygen containing gas such as air or chlorine gas can be used at between .01- .1 volume percent to prolong the life of the catalyst.
The isomerization step is also achievable in a liquid phase process in the presence of a homogenous catalyst preferably selected from compounds of group 3, 4, 5, 13, 14 and 15 metal compounds of the Periodic Table of the elements (IUPAC 1988) and their mixtures (groups of the Periodic Table of the elements which were previously called IIIA, IVa, IVb, Va, Vb and VIb). The compounds of the metals are intended to include hydroxides, oxides and the organic or inorganic salts of these metals, as well as mixtures thereof. Preferred are the aluminum, titanium, tantalum, molybdenum, boron, tin and antimony derivatives such as A1C13, TiCl4, TaCl5, Mod , BF3, SnCl4, and SbC15. In the process according to the invention the preferred derivatives of the metals are the salts and these are preferably chosen from the halides and more particularly from chlorides, fluorides and chlorofluorides such as A1F3, TiF4, TaF5, MoF6, SnF4, SbFs, SbFxCly (x+y)=5. The catalyst must be subjected to activation (by HF or any molecule able to exchange fluorine) prior to the isomerization step. In the case of antimony type catalyst, a low level of chlorine gas as oxidizing agent can be used to maintain the antimony catalyst in the pentavalent oxidation state. In addition to the above mentioned Lewis acids catalyst, an ionic liquid derived from antimony, titanium, niobium and tantalum is suitable for liquid phase fluorination processes. A description of the preparation of such catalysts is disclosed in the US Patent No. 6,881,698.
The homogenous catalyst for a liquid phase process can also be selected from the Bronsted type family of acids such as (but not limited to) sulfuric acid H2S04, sulfonic type acids such as CISO3H or FSO3H or triflic acid CF3SO3H or methane sulfonic acid CH3SO3H. For the liquid phase process, the operating temperature can be varied between about 20-200°C, with a contact time between about 0.5-50 hours
Isomerization can also be accomplished, in the primary 1233zd reactors- either in the gas or liquid phase. This allows the separated Z-1233zd to be recycled back to the primary reactors and avoids the need for separate isomerization reactors, RI-1 and RI- 2. See figures 3 and 4. It is believed this recycle would result in the Z-1233zd levels building to an equilibrium limit, after which the Z-1233zd would isomerizes in RFL-1 or RFG-2 at the same rate that it was being formed.
The process of the present invention may comprise additional separation steps between each step. The purpose of theses separations could be:
1. to remove, totally or partially, any hydracid (HF, HC1) from the flow if required, or
2. to isolate a desired product in order to feed it in a subsequent step, or
3. to purify a product and removes organic impurities or by products, or
4. to dry a product (H20 removal).
The means used to achieve these additional steps are known in the art and include but are not limited to: distillation, extractive distillation or adsorption. The process of the present invention is exemplified in the figures, which set forth block flow diagrams of gas phase and liquid phase processes in accordance with the present invention. The processes in the figures are set out in the form of process modules designed to achieve a specific purpose and arranged in accordance with the process of the present invention. Theses modules comprise:
RFL- comprises a liquid phase fluorination reactor and rectification system comprising an unagitated, jacketed pressure vessel connected to a rectification column. The reactor also acts as the reboiler of the rectification column. The HF and organic (1230za) are fed directly to the reactor. The molar feed ratio of HF to organic is dictated by the reaction stoichiometry and the amount of HF leaving the reactor with the rectification column overhead and liquid phase purges. Mixing is provided by the boiling action of the reactor contents. For the most part, the reactor effluent leaves the reactor vessel as a gas and enters the bottom of the rectification column. A small purge from the liquid phase can remove any non-volatiles that may form during the reaction. The rectification column contains either packing or trays designed to provide good mass transfer between up flowing gas and down flowing liquid. The condenser at the top of the column is cooled by either cooling water, chilled water, or some type of refrigeration. The condenser is a partial condenser where the liquid effluent is refluxed directly back to the column. The vapor effluent consists of HCl, HF and organic components.
DH- comprises an HCl distillation system whereby pure HCl is removed from the top of a distillation column. This column can operate between 100 psig and 300 psig. More typically, the HCl is distilled above 120 psig to allow the use of conventional (- 40C) refrigeration at the top of the HCl column. The bottoms of this column contains HF and organic with a small residual amount of HCl. The ratio of HF to the organic component typically is close to the azeotropic composition.
PS- comprises a liquid phase separator to separate two liquid phases, one consisting primarily of a hydrochlorofluorocarbon (HCFC) and the other consisting primarily of HF. The HF phase is usually the less dense so that it exits from the top of the phase separator and the HCFC exits as the bottom phase. There is some HF in the HCFC phase and some HCFC in the HF phase. However, the compositions of both phases are far removed from any azeotropic composition. The operating temperature of the phase separator can be between -40°C and +20°C. However, the lower the temperature, the better the phase separation.
DA- comprises an azeotropic distillation column which distills overhead an azeotropic composition of HF and an organic consisting of one or more HCFC's
(hydrochlorofluorocarbons) and HFC's (hydrofluorocarbons). These organic compounds can be either saturated or olefinic. The bottoms composition is either entirely HF or entirely organic, depending on whether the column feed composition is on the HF rich side or the organic rich side of the azeotrope. If the bottoms are HF, this stream is normally recycled back to the reactor. If the bottoms steam is organic, it is sent to a conventional distillation train.
DS- comprises a straight distillation normally done under pressure.
RI -comprises a gas phase isomerization reaction typically done at temperatures above 400°C in an adiabatic, packed bed reactor. The module consists of a feed vaporizer and superheater. It can include an "economizer", whereby hot effluent is fed to one side and relatively cold reactor feed gases are fed to another side of a heat exchanger. The effluent gases are further cooled before entering a distillation column. Isomerization reactions can be run at varying conversions depending on the equilibrium distribution of isomers. The effluent isomers can have boiling points very close together. However, they typically exhibit close to ideal behavior so can be separated by conventional distillation. As an alternative to the gas phase, this reaction can be done as a homogeneously catalyzed liquid phase reaction. In this
configuration, the reactor would be a continuous stirred tank with the effluent being removed as a vapor to effect separation from the catalyst.
RFG- comprises a gas phase fluorination reactor that is an adiabatic packed bed reactor that feeds a gas phase over a solid catalyst. No cooling is needed because of the reactor has a low conversion per pass and a high HF molar feed ratio. The adiabatic exotherm is typically less than 100°C. The feed HF and organic are vaporized in a common vaporizer and superheated to the reactor temperature. The common vaporizer allows the 1230za and/or 240fa to be vaporized at a lower temperature than would be possible if it were vaporized as a pure component, thereby minimizing thermal degradation. This module can also include an "economizer", whereby hot effluent is fed to one side and relatively cold reactor feed gases are fed to another side of a heat exchanger. The effluent gases are further cooled before entering a distillation column. Reaction temperatures are between 200°C and 400°C. The pressure is high enough to allow the HC1 by-product to be distilled with conventional refrigeration- preferably between 100 psig and 200 psig. The lower case letter used to identify the modules distinguishes multiple appearances of the same type of module in the same process.
Figure 1 is a block flow diagram of a process in accordance with the present invention for converting 1230za to E-1233zd using a liquid phase fluorination step. The Figure incorporates the process modules described above. Figure 1 discloses a process wherein 1230za and HF are fed to reaction module RFL-1. Typically, the reaction takes place in a predominantly HF rich medium without a catalyst. The HC1 and the 1233zd/HF exit the top of the rectification column of RFL-1. The vapor effluent of RFL-1 enters DH-1 to remove HC1 as a pure overhead product. The bottoms of DH-1 consists primarily of 1233zd (both E and Z isomers) and HF at a near azeotropic composition. This is fed to module PS- 1 to effect a liquid phase separation. The top HF rich phase is sent to module DA- la, where HF is separated as a bottoms stream for recycle to the reactor. The overhead azeotrope of 1233zd and HF is recycled back to DH-1 to allow any residual HC1 and light organics to be stripped out in this column before the azeotrope gets recycled to phase separation. The bottoms stream from PS- 1 goes to module DA- lb, which removes an organic stream devoid of HF as a bottoms stream. The overhead from DA- lb is recycled to DH-1 for the same reason that the DA- la azeotrope was recycled to DH-1. The bottoms of DA- lb is sent to process module DS-1 that separates any heavies from the 1233zd. The overhead from DS-1 is E-1233zd, the desired trans isomer. The Z-1233zd is higher boiling and is recovered for feeding to process module RI-1. The effluent from the isomerization reactor is recycled to DS-1, which effects the separation of the E and Z isomers.
Alternatively, Z-1233zd from DS-1 could be recycled directly to RFL-1 as shown in Figure 3, where isomerization could occur so as to limit the Z-1233zd concentration in RFL-1 to an equilibrium level. Figure 2 is a block flow diagram of a process in accordance with the present invention for converting 1230za or 240fa to E-1233zd using a gas phase fluorination step. The Figure incorporates the process modules described above. In Figure 2 the process is similar to Figure 1 except, for example, the liquid phase fluorination reactor (RFL-1) is replaced by a gas phase fluorination reactor (RFG-1) and azeotropic distillation column (DA-2a).
The process as outlined by Figure 2 comprises feeding 1230za and/or 240fa and HF to reaction module RFG-2. The reaction takes place in a gas phase with a catalyst. The reactor effluent consists of predominantly HC1, 1233zd, unreacted 1230za and excess HF. The reactor effluent of RFG-2 enters DA-2a to remove HF and unreacted F1230za as bottoms that is recycled to the reactor. The overhead, which consists predominantly of HC1 and the azeotrope of HF and 1233zd (both E and Z isomers), is sent to DH-2, which removes HC1 as a pure overhead product. The bottoms of DH-2 consists of primarily 1233zd (both E and Z isomers) and HF at a near azeotropic composition. This is fed to module PS-2 to effect a liquid phase separation. The top HF rich phase is sent to module DA-2b, where HF is separated as a bottoms stream for recycle to the reactor. The overhead azeotrope of 1233zd and HF is recycled back to DH-2 to allow any residual HC1 and light organic s to be stripped out in this column before the azeotrope gets recycled to phase separation. The bottoms stream from PS- 2 goes to module DA-2c, which removes an organic stream devoid of HF as a bottoms stream. The overhead from DA-2c is recycled to DH-2 for the same reason that the DA-2b azeotrope was recycled to DH-2. The bottoms of DA-2c is sent to process module DS-2 that separates any heavies from the 1233zd. The overhead from DS-2 is E-1233zd- the desired trans isomer. The Z-1233zd is higher boiling and is recovered for feeding to process module RI-2. The effluent from the isomerization reactor is recycled to DS-2, which effects the separation of the E and Z isomers.
Alternatively, Z-1233zd could be recycled directly to RFG-2 as shown in Figure 4, where isomerization could occur so as to limit the Z-1233zd concentration in RFG-2 to an equilibrium level.

Claims

What we claim
1. A process for manufacturing trans 1- chloro 3,3,3 trifluoro propene (E-1233zd) from 1,1,3,3- tetrachloropropene (1230za) and/ or 1,1,1,3,3-pentachloropropane (240fa) comprising the steps of: fluorination of 1,1,3,3- tetrachloropropene (1230za) and/ or 1,1,1,3,3- pentachloropropane (240fa) to a mixture comprising cis 1233zd (Z-1233zd) and trans 1233zd (E- 1233zd); followed by separation of said cis 1233zd (Z-1233zd) from said trans 1233zd (E- 1233zd); followed by recycling said cis 1233zd (Z-1233zd) to said fluorination step where said cis 1233zd (Z-1233zd) is isomerized to form trans 1233zd (E- 1233zd).
2. The process of claim 1 wherein said fluorination step is carried out in the gas phase or the liquid phase.
3. The process of claim 2 wherein said fluorination step is carried out in a liquid phase with a homogenous catalysts selected from the group consisting of soluble Lewis acid catalysts and Bronsted acid catalysts.
4. The process of claim 3 wherein said soluble Lewis acid catalyst is selected from Sbv; TiIV; SnIV; MoVI; Nbv; Tav; oxide supported catalysts; fluorinated alumina;
fluorinated chromia; prefluorinated activated carbon; graphite carbon; SiC; Sb5.
5. The process of claim 4 wherein said oxide supported catalyst is selected from the group consisting of AI2O3 and Ti02.
6. The process of claim 3 wherein said Bronsted acid catalyst is selected from the group consisting of triflic acid, methane sulfonic acid, sulfuric acid and sulfonic acid.
7. The process of claim 2 wherein said isomerization is carried out in the gas phase with a high surface area heterogeneous Cr catalyst, supported or unsupported.
8. The process of claim 7 wherein said catalyst further comprising a co-catalyst selected from the group consisting of Co, Ni, Zn and Mn.
EP15743421.8A 2014-01-29 2015-01-28 Process for the manufacture of hydrochlorofluoroolefins Withdrawn EP3099655A4 (en)

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US20180194703A1 (en) * 2017-01-06 2018-07-12 Honeywell International Inc. Systems and methods for separating (e)-1-chloro-3,3,3-trifluoropropene, hf, and a heavy organic and reactor purge
MX2021005775A (en) * 2018-11-15 2021-07-02 Arkema Inc Method to purify a crude stream containing hydrochlorofluoroolefi n.
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US5710352A (en) * 1996-09-19 1998-01-20 Alliedsignal Inc. Vapor phase process for making 1,1,1,3,3-pentafluoropropane and 1-chloro-3,3,3-trifluoropropene
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US8987534B2 (en) * 2008-11-19 2015-03-24 Arkema Inc. Process for the manufacture of hydrochlorofluoroolefins
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