WO2011107188A2 - Process for the manufacture of a 1,2-epoxide and a device for carrying out said process - Google Patents

Process for the manufacture of a 1,2-epoxide and a device for carrying out said process Download PDF

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Publication number
WO2011107188A2
WO2011107188A2 PCT/EP2011/000320 EP2011000320W WO2011107188A2 WO 2011107188 A2 WO2011107188 A2 WO 2011107188A2 EP 2011000320 W EP2011000320 W EP 2011000320W WO 2011107188 A2 WO2011107188 A2 WO 2011107188A2
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Prior art keywords
aqueous phase
process according
reactor
reaction mixture
terminal olefin
Prior art date
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Ceased
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PCT/EP2011/000320
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French (fr)
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WO2011107188A3 (en
Inventor
Prasad Muppa
Ron Postma
Bart Van Den Berg
Juergen Stock
Holger Wiederhold
Hans Rausch
Jörg SCHALLENBERG
Stefan Bernhardt
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Hexion Research Belgium SA
Hexion Inc
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Momentive Specialty Chemicals Research SA
Momentive Specialty Chemicals Inc
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Priority to KR1020147029535A priority Critical patent/KR101622504B1/en
Priority to CN201180008055.1A priority patent/CN102844310B/en
Priority to AU2011223288A priority patent/AU2011223288B2/en
Priority to KR1020127022622A priority patent/KR101475579B1/en
Priority to RU2012137285/04A priority patent/RU2540864C2/en
Priority to BR112012019183A priority patent/BR112012019183A8/en
Priority to EP11702144A priority patent/EP2539329A2/en
Priority to US13/574,715 priority patent/US8859790B2/en
Application filed by Momentive Specialty Chemicals Research SA, Momentive Specialty Chemicals Inc filed Critical Momentive Specialty Chemicals Research SA
Priority to JP2012551532A priority patent/JP6000856B2/en
Priority to KR1020147008554A priority patent/KR20140056381A/en
Publication of WO2011107188A2 publication Critical patent/WO2011107188A2/en
Publication of WO2011107188A3 publication Critical patent/WO2011107188A3/en
Anticipated expiration legal-status Critical
Priority to US14/184,412 priority patent/US9102640B2/en
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D301/00—Preparation of oxiranes
    • C07D301/02—Synthesis of the oxirane ring
    • C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
    • C07D301/12—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with hydrogen peroxide or inorganic peroxides or peracids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D301/00—Preparation of oxiranes
    • C07D301/02—Synthesis of the oxirane ring
    • C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
    • C07D301/14—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with organic peracids, or salts, anhydrides or esters thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
    • B01D17/02—Separation of non-miscible liquids
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
    • B01D17/02—Separation of non-miscible liquids
    • B01D17/0208—Separation of non-miscible liquids by sedimentation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F25/00—Flow mixers; Mixers for falling materials, e.g. solid particles
    • B01F25/40—Static mixers
    • 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
    • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/18—Stationary reactors having moving elements inside
    • 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
    • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/24—Stationary reactors without moving elements inside
    • B01J19/2415—Tubular reactors
    • B01J19/2435—Loop-type reactors
    • 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
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B01J31/1815—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine
    • B01J31/182—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine comprising aliphatic or saturated rings
    • 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
    • B01J4/00—Feed or outlet devices; Feed or outlet control devices
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D301/00—Preparation of oxiranes
    • C07D301/02—Synthesis of the oxirane ring
    • C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F25/00—Flow mixers; Mixers for falling materials, e.g. solid particles
    • B01F25/40—Static mixers
    • B01F25/42—Static mixers in which the mixing is affected by moving the components jointly in changing directions, e.g. in tubes provided with baffles or obstructions
    • B01F25/43—Mixing tubes, e.g. wherein the material is moved in a radial or partly reversed direction
    • B01F25/431—Straight mixing tubes with baffles or obstructions that do not cause substantial pressure drop; Baffles therefor
    • 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
    • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049—Controlling or regulating processes
    • B01J2219/00051—Controlling the temperature
    • B01J2219/00074—Controlling the temperature by indirect heating or cooling employing heat exchange fluids
    • B01J2219/00087—Controlling the temperature by indirect heating or cooling employing heat exchange fluids with heat exchange elements outside the reactor
    • B01J2219/00094—Jackets
    • 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
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/70—Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues
    • 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
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/70—Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues
    • B01J2231/72—Epoxidation
    • 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
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0213—Complexes without C-metal linkages
    • B01J2531/0216—Bi- or polynuclear complexes, i.e. comprising two or more metal coordination centres, without metal-metal bonds, e.g. Cp(Lx)Zr-imidazole-Zr(Lx)Cp
    • 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
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/70—Complexes comprising metals of Group VII (VIIB) as the central metal
    • B01J2531/72—Manganese
    • 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
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/90—Catalytic systems characterized by the solvent or solvent system used
    • B01J2531/96—Water
    • 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 the manufacture of a 1 ,2-epoxide in the presence of a water-soluble manganese complex as an oxidation catalyst and to a device for carrying out said process.
  • a process for the manufacture of a 1 ,2-epoxide is described in the published European patent application EP 2149569. It describes the catalytic oxidation of a terminal olefin using a water soluble manganese complex as the oxidation catalyst.
  • a multiphasic e.g. biphasic system
  • a system comprising an organic phase, which may be a liquid or a gaseous phase, and an aqueous phase.
  • the actual reaction takes place in the aqueous phase, while the resulting epoxide product separates from the aqueous phase into the organic phase due to low solubility of, or extraction or stripping by the organic phase.
  • the 1 ,2-epoxide is produced at high turnover numbers (TON), with high selectivity towards the 1,2-epoxide with moreover improved ease of isolating the produced 1,2-epoxide.
  • the catalyst system used to achieve the above advantages comprises a manganese atom or a number of manganese atoms coordinated with a ligand or ligands.
  • binuclear manganese complexes are binuclear manganese complexes.
  • EP 2149570 describes the oxidation of allyl chloride to produce epichlorohydrin.
  • EP 2149569 denotes further that the process may be carried out in a reactor, but does not elaborate on this. It turned out, however, that upon isolation of the 1,2-epoxide, an aqueous phase was left which comprised an active catalyst fraction.
  • EP 2149569 does not describe any further use for this fraction, meaning that part of the catalyst is wasted, which is not efficient.
  • Another example about a manufacturing method of propylene oxide is presented in the non-published European patent application 09075528. Disclosure of the Invention
  • Yet another object if this invention is to provide a reactor which is as small as possible while having the same improved productivity per reactor volume.
  • a process for the manufacture of an epoxide including adding an oxidant, a water-soluble manganese complex, and a terminal olefin to form a multiphasic reaction mixture, wherein the water-soluble manganese complex is a mononuclear species of the general formula (I): [LMnX 3 ]Y (I), or a binuclear species of the general formula (II): [ ⁇ ( ⁇ - ⁇ ) 3 ⁇ ,]( ⁇ ) ⁇ (II), wherein Mn is a manganese; L or each L independently is a polydentate ligand, each X independently is a coordinating species and each ⁇ - ⁇ independently is a bridging coordinating species, and wherein Y is a non- coordinating counter ion, reacting the terminal olefin with the oxidant in the multiphasic reaction mixture having at least one organic phase in the presence of the water-soluble manganese complex, separating the reaction mixture into the at least one organic phase in the presence of the water
  • FIG. 1 illustrates a schematic representation of an embodiment of a device for the manufacture of epichlorohydrin.
  • the invention is based on the observation that the separated aqueous phase contains catalyst which is still active. This has led the current inventors to the insight that reusing at least part of the separated aqueous phase comprising the catalyst, leads to a more efficient use of the catalyst, and lower energy consumption in subsequent separating steps.
  • the combination of a well dispersed biphasic reaction system and reuse of the aqueous phase may lead to a high turn over number, (TON), which is the number of moles of terminal olefin a mole of catalyst can convert before becoming inactivated. Said combination may further lead to a minimized energy consumption for subsequent separation and purification steps, high selectivity towards product for all raw materials and effective usage of reactor volume leading to a less complicated process.
  • TON turn over number
  • the process is carried out in a multiphasic system of an aqueous phase and at least one organic phase.
  • the oxidation (step a)) of the terminal olefin is believed to take place in an aqueous phase, whereas the organic phase is believed to extract or strip produced 1 ,2-epoxide from the water phase.
  • the inventors have found that the organic phase contains little or no water soluble byproducts and catalyst. It is beneficial to use a terminal olefin which has limited solubility in water, for example, allyl chloride and allyl acetate instead of conventionally used allyl alcohol.
  • the multiphasic system may be created by adding the terminal olefin with limited solubility to an aqueous phase in an amount greater than what dissolves in the aqueous phase.
  • Preferred terminal olefins have a maximum solubility of about 100 g/L (at 20°C), more preferably of from 0.01 to 100 g/L.
  • the volumetric ratio of the organic phase to the aqueous phase, both inside the reactor, and the degree of contact between the phases are important parameters in the performance of the catalyst system. If the amount of organic phase is too high, the aqueous phase is no longer the continuous phase. In this case, there may be insufficient mixing of the ingredients. This means that the conversion rate of terminal olefin is considerably lowered. On the other hand, if the aqueous phase inside the reactor is too high with respect to the amount of organic phase, the terminal olefin concentration in the aqueous phase will be too low with respect to oxidant concentration. This may lead to the production of undesirable side products and catalyst deactivation. Therefore the volumetric ratio of aqueous phase to organic phase inside the reactor is preferably in the range of from 10:1 to 1 :5, with emulsion formation as a maximum limit.
  • the above limitations can also be influenced by the degree of mixing.
  • the reaction catalytic oxidation of the terminal olefin and the oxidant in the presence of the catalyst may occur (step a)).
  • the resulting reaction mixture is discharged from the reactor.
  • the discharged reaction mixture comprises both product and unreacted starting material.
  • the discharged reaction mixture is allowed to settle into its separate phases, the aqueous phase and the at least one organic phase.
  • the at least one organic phase may comprise two organic phases, such as one dispose below and one disposed above the aqueous phase.
  • the aqueous phase contains catalyst which is still active.
  • the catalyst contained within the separated aqueous phase can be reused, thereby increasing the catalyst efficiency.
  • the aqueous phase contains at least trace amounts of the terminal olefin. Without being bound to any theory, it is believed that the presence of terminal olefin allows the catalyst to remain active, whereas it is believed that without the presence of terminal olefin and/or due to the presence of the epoxide and/or oxidant without terminal olefin present the activity of the active catalyst reduces. Cooling may also be used to reduce the decrease in catalyst efficiency.
  • the aqueous phase can be reused by feeding at least a portion (part) of the separated aqueous phase to a next reactor or by recycling at least a portion of the separated aqueous phase to the same reactor (step d)).
  • the at least a portion of the aqueous phase is recycled into the reaction mixture. This way, catalyst present in the recycled aqueous phase is not discharged, but efficiently used again.
  • aqueous starting materials such as the oxidant, catalyst and, if needed, buffer, are supplied to the reaction mixture (step a)).
  • aqueous starting materials are indicated as the aqueous components.
  • a certain volume of separated aqueous phase is recycled into the reaction mixture.
  • the mass ratio of the volume of aqueous components to the volume of recycled aqueous phase added to the reaction mixture at every instant is indicated as the water recycle ratio.
  • said water recycle ratio preferably is in the range of from 10:1 to 1 :10, more preferably of from 2:1 to 1 :5 and most preferably 1 :3.5.
  • turbulent conditions such as a high velocity of the aqueous phase will prevent agglomeration of the organic droplets dispersed in said medium.
  • the molar ratio of terminal olefin to oxidant is very important in the process of the current invention.
  • the molar ratio of terminal olefin to oxidant may be greater than 1 :2.
  • this ratio is in the range of from 12:1 to 1:1. More preferably, this ratio may be 1 :1, 1.2:1, 2:1, or 4:1, or 2:1 to 12:1. If too much oxidant is used, then the selectivity towards the 1,2-epoxide reduces due to the production of undesirable side-products. Another consequence of too much oxidant with respect to terminal olefin is rapid catalyst deactivation. If not enough oxidant is used, then the turnover number is suboptimal.
  • the oxidant is preferably added to the aqueous phase at a rate about equal to the reaction rate of the catalytic oxidation.
  • the reaction is carried out using hydrogen peroxide, or a precursor thereof, as an oxidant.
  • Hydrogen peroxide has strong oxidizing properties. It is typically used in an aqueous solution. The concentration of hydrogen peroxide may vary, from 15% (e.g., consumer grade for bleaching hair) to 98% (propellant grade), with a preference for industrial grades varying from 30 to 70%. More preferably, the concentration of hydrogen peroxide is 70%.
  • Other oxidants that may be used include organic peroxides, peracids, and combinations thereof.
  • the reaction (catalytic oxidation) of the terminal olefin takes place in the aqueous phase.
  • the aqueous phase may have a pH from 1 to 8, such as from 2 to 5.
  • the aqueous phase may further comprise a buffer system to stabilize the pH in a certain range. For instance, it has been found advantageous that the aqueous phase is stabilized in a pH range of from 1 to 8, more preferably of from 2 to 5.
  • the pH is therefore (well) below that used when bleaching olefins with hydrogen peroxide as the oxidant, typically carried out at more alkaline conditions (e.g., pH adjusted with NaHC0 3 to 9.0).
  • the suitable or preferred range may be achieved by several known acid-salt combinations, with the preferred combination being based on oxalic acid-oxalate salt, acetic acid-acetate salt, malonic acid-malonate salt, and combinations thereof.
  • the aqueous phase may further comprise minor amounts, if any, of other organic compounds.
  • the aqueous phase may also contain minor amounts of co-solvents, e.g. to increase the solubility of the olefin.
  • co-solvents include, for example, acetone, methanol, and other water-soluble alcohols. Co-solvents may be used in amounts such as to keep a biphasic system, preferably in an amount ⁇ 10 weight percent.
  • the aqueous phase may further comprise a phase transfer agent and/or a surfactant, in particular if a terminal olefin is used with low solubility (e.g., below 0,1 g/L water).
  • phase transfer agents that may be used in the process of the invention include quaternary alkyl ammonium salts.
  • surfactants that may be used in the process of the invention include non ionic surfactants such as Triton XI 00TM available from Union Carbide.
  • the catalyst system comprising a water soluble manganese complex is described as follows.
  • the oxidation catalyst is a water soluble manganese complex.
  • the manganese complexes include mononuclear species of the general formula (I):
  • the non- coordinating counter ion Y may provide for the charge neutrality of the complex and the value of n depends upon the charge of the cationic complex and anionic counter ion Y, for example, n may be 1 or 2. In one embodiment, an ion of CH 3 COO " or PF " may be used as the non- coordinating counter ion.
  • Ligands which are suitable for the present invention are acyclic compounds containing at least 7 atoms in the backbone or cyclic compounds containing at least 9 atoms in the ring, each having the nitrogen atoms separated by at least two carbon atoms.
  • a preferred class of ligands is that based on (substituted) triazacyclononane ("Tacn").
  • the preferred ligand is l,4,7-trimethyl-l,4,7,-triazacyclononane (“TmTacn").
  • Dinuclear manganese complexes are denoted as preferred, because of their greater activity and solubility in water.
  • Preferred dinuclear manganese complexes are those of the formula [ ⁇ ⁇ 2 ( ⁇ -0)3 ⁇ 2 ]( ⁇ ) ⁇ (same as formula: [LMn ⁇ -0) 3 MnL](Y) n ), wherein n is 2, and L and Y have the meaning identified above, preferably TmTacn as ligand, and PF 6 " or acetate (CH 3 C0 2 " , hereinafter OAc) as counterion.
  • the catalyst system comprising a water soluble manganese complex is described above.
  • the preferred complex for the current invention comprises l,4,7-trimethyl-l,4,7,-triazacyclononane ("TmTacn”) as the preferred ligand or ligands. This ligand is commercially available from Aldrich.
  • the manganese complex is used in catalytically effective amounts.
  • the catalyst is used in a molar ratio of catalyst (Mn) to the oxidant of from 1 :10 to 1 :10,000,000, preferably of from 1 :100 to 1 :1,000,000, most preferably of from 1 :1000 to 1 :100,000.
  • Mn catalyst
  • the amount of catalyst may also be expressed in terms of its concentration, when keeping in mind the volume of the aqueous medium. For instance, it may be used in a molar concentration (based on the Mn) of from 0.001 to 10 mmol/L, preferred of from 0.01 to 7 mmol/L and most preferably of from 0.01 to 2 mmol/L.
  • the reaction conditions for the catalytic oxidation may be quickly determined by a person skilled in the art.
  • the reaction is exothermic, and cooling of the reaction mixture may be required.
  • the reaction is preferably carried out at temperatures anywhere from -5°C to 40°C, dependent upon such physical parameters as melting and boiling point of the used terminal olefins.
  • the terminal olefin used is an epoxidizible olefin which may be functionalized.
  • the terminal olefin may be a liquid under process conditions, e.g., allyl chloride or liquefied propylene, but also a gas, e.g. gaseous propylene.
  • terminal olefins examples include terminal olefinically unsaturated compounds.
  • terminal olefinically unsaturated compounds therefore include the following compounds:
  • R is a radical of 1 or more carbon atoms optionally comprising 1 or more heteroatoms (such as oxygen, nitrogen or silicon);
  • R' is a multivalent radical of 1 or more carbon atoms optionally comprising 1 or more heteroatoms wherein n corresponds with the valence of the multivalent radical;
  • X is a halogen atom, and
  • Y is an oxygen atom.
  • olefinically unsaturated compounds selected from the compounds:
  • the terminal olefin may have limited solubility in water, for example, the terminal olefin may have a maximum solubility in the aqueous phase at 20°C of about 100 g/L, more preferably of from 0.01 to 100 g/L at 20°C.
  • the terminal olefin is selected from allyl bromide, allyl chloride and allyl acetate.
  • allyl chloride is used for the manufacture of epichlorohydrin, because of the commercial interest and ease of isolating the produced epichlorohydrin.
  • the terminal olefin is propylene in order to produce propylene oxide, and the reaction is carried out at temperatures in the range from -5°C to 40°C. Propylene is preferably used in excess over the oxidant.
  • the buffer, if any, and oxidation catalyst are fed as a pre-mixed mixture into step a).
  • the device comprises a reactor for performing the catalytic oxidation having an inlet for feeding the oxidant, the oxidation catalyst, optionally a buffer and the terminal olefin to the reactor, and an outlet for discharging the reaction mixture from said reactor, separating means connected to the reactor outlet for separating the reaction mixture into the at least one organic phase and an aqueous phase, recycling means for recycling part of the aqueous phase separated in the separating means, dispersing means for dispersing the terminal olefin into the aqueous phase and cooling means for controlling the temperature of the catalytic oxidation process.
  • the device comprises a reactor for carrying out the process having an inlet and an outlet. Via the reactor inlet the reactants are fed to the reactor, whereas via the reactor outlet the reaction mixture is discharged.
  • the device further comprises separating means connected to the reactor outlet for separating the reaction mixture into the at least one organic phase and the aqueous phase as explained above.
  • this separation means comprises a straight forward liquid to liquid separator, such as a settling tank, since the product forms at least one separate organic phase which phase separates from the aqueous phase when allowed to settle.
  • Other devices such as hydrocyclones can also be used.
  • the aqueous phase is recycled into the reactor via the inlet of the reactor.
  • This recycling means may be of simple design, e.g. a pipe connecting an aqueous phase outlet of the separation means and the reactor inlet equipped with a pump to transport the aqueous phase into the reactor. It is noted here that the skilled person will be aware that the reactor according to the invention is equipped with standard process technological elements like e.g. pumps, valves and control mechanisms.
  • the reactor according to the invention further comprises dispersing means for dispersing the organic terminal olefin phase into the aqueous phase and cooling means for controlling the temperature of the catalytic oxidation, because of its exothermic nature.
  • the reactor may be a plug flow reactor (PFR). Due to the required high velocity for dispersing and the long residence times a PFR used in the present invention will be a very long PFR.
  • the reactor may also be a continuous stirred tank reactor (CSTR). When using a CSTR, special care should be taken in dispersing the terminal olefin into the aqueous phase.
  • the catalytic oxidation may also be carried out in a loop reactor.
  • a loop reactor the reaction mixture is circulated.
  • the circulation rate of the loop reactor is about 15 times the rate at which the aqueous components and the terminal olefin is fed, i.e. the feed rate
  • the loop reactor can be described as a CSTR because of the high degree of back mixing.
  • the advantage of using a loop reactor in the present process is that it allows for the well defined mixing behaviour of a pumped system combined with dispersing means in a compact reactor design.
  • the dispersing means is a static mixer, since this mixer will provide maximum break up of organic droplets in the continuous aqueous phase.
  • fresh oxidant and olefin are fed to the aqueous phase in subdivided portions to the reactor through multiple inlet parts distributed over the reactor housing.
  • FIG. 1 shows a schematic representation of an embodiment of a device for the manufacture of epichlorohydrin.
  • the device 10 comprises a loop reactor 20 comprising an inlet 21 and an outlet 22. Hydrogen peroxide, a water soluble manganese complex as the oxidation catalyst, an oxalate buffer solution and allyl chloride, which are disposed in separate feeding tanks 15, are fed to the reactor 20.
  • the reactants are transported from the feeding tanks 15 to the reactor inlet 21 through feeding conduits 11 by means of feeding pumps 12.
  • a pre-mixing means 50 may be disposed between the inlet 21 and one or more of the feeding pumps 12 to pre-mix some of the components, such as the catalyst and oxalate buffer in FIG 1.
  • the reactor inlet 21 advantageously comprises several inlet ports, one port for each reactant.
  • the reaction mixture is discharged from the reactor 20 via the reactor outlet 22 into a separating means 30.
  • the reactor outlet 22 and separating means 30 are connected via a discharge conduit 13.
  • the separating means 30 comprises a separation inlet 31 through which the reaction mixture is supplied to the separating means 30.
  • the organic phase comprising epichlorohydrin is isolated from the separating means 30 through the product outlet 32.
  • At least part of the aqueous phase in the separating means 30 is recycled to the reactor 20 via a recycling conduit 41 connecting a recycling outlet 33 of separating means 30 and reactor inlet 21.
  • a recycling pump 42 is comprised in the recycling conduit 41 to transport the aqueous phase.
  • the organic phase inside the reactor 20 is dispersed in the aqueous phase using a dispersing means 23.
  • the reactor 20 further comprises a reactor pump 26 for transporting the reaction mixture and cooling means 24 to cool the reaction mixture.
  • Said cooling means 24 may be e.g. a water cooler or other types of heat exchanging means. However, the choice of the type of cooling means 24 is left to the expertise of the skilled person.

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Abstract

Apparatus and processes are provided for forming epoxide compounds. In one embodiment, a process for the manufacture of an epoxide is provided including adding an oxidant, a water-soluble manganese complex and a terminal olefin to form a multiphasic reaction mixture, reacting the terminal olefin with the oxidant in the multiphasic reaction mixture having at least one organic phase in the presence of the water-soluble manganese complex, separating the reaction mixture into the at least one organic phase and an aqueous phase, and reusing at least part of the aqueous phase. The invention is also related to a device for performing the above process.

Description

Process for the manufacture of a 1,2-epoxide and a device for carrying out said process Field of invention
The invention relates to the manufacture of a 1 ,2-epoxide in the presence of a water-soluble manganese complex as an oxidation catalyst and to a device for carrying out said process.
Background of invention
A process for the manufacture of a 1 ,2-epoxide is described in the published European patent application EP 2149569. It describes the catalytic oxidation of a terminal olefin using a water soluble manganese complex as the oxidation catalyst.
The process described is carried out in a multiphasic, e.g. biphasic system, i.e. a system comprising an organic phase, which may be a liquid or a gaseous phase, and an aqueous phase. The actual reaction takes place in the aqueous phase, while the resulting epoxide product separates from the aqueous phase into the organic phase due to low solubility of, or extraction or stripping by the organic phase. For this reason, the 1 ,2-epoxide is produced at high turnover numbers (TON), with high selectivity towards the 1,2-epoxide with moreover improved ease of isolating the produced 1,2-epoxide.
Typically the catalyst system used to achieve the above advantages comprises a manganese atom or a number of manganese atoms coordinated with a ligand or ligands. Of particular interest are binuclear manganese complexes. As an example of the above manufacture of 1,2- epoxide, reference is made to the European patent application publication EP 2149570, which describes the oxidation of allyl chloride to produce epichlorohydrin. EP 2149569 denotes further that the process may be carried out in a reactor, but does not elaborate on this. It turned out, however, that upon isolation of the 1,2-epoxide, an aqueous phase was left which comprised an active catalyst fraction. EP 2149569 does not describe any further use for this fraction, meaning that part of the catalyst is wasted, which is not efficient. Another example about a manufacturing method of propylene oxide is presented in the non-published European patent application 09075528. Disclosure of the Invention
It is therefore an object of the current invention to provide a process with improved catalyst efficiency.
It is another object of the invention to provide a process with improved selectivity towards the product.
It is yet another object of the invention to provide a process with low energy requirements for separation and purification steps.
It is still another object of this invention to provide a device, e.g. a reactor, to carry out the manufacture of the 1 ,2-epoxide.
Yet another object if this invention is to provide a reactor which is as small as possible while having the same improved productivity per reactor volume.
One or more of the above objects are achieved by a process for the manufacture of an epoxide, including adding an oxidant, a water-soluble manganese complex, and a terminal olefin to form a multiphasic reaction mixture, wherein the water-soluble manganese complex is a mononuclear species of the general formula (I): [LMnX3]Y (I), or a binuclear species of the general formula (II): [ίΜη(μ-Χ)3ΜηΙ,](Υ)η (II), wherein Mn is a manganese; L or each L independently is a polydentate ligand, each X independently is a coordinating species and each μ-Χ independently is a bridging coordinating species, and wherein Y is a non- coordinating counter ion, reacting the terminal olefin with the oxidant in the multiphasic reaction mixture having at least one organic phase in the presence of the water-soluble manganese complex, separating the reaction mixture into the at least one organic phase and an aqueous phase, and reusing at least part of the aqueous phase.
Detailed Description of the Figures
The following is a brief description of figures wherein like numbering indicates like elements. FIG. 1, illustrates a schematic representation of an embodiment of a device for the manufacture of epichlorohydrin.
Mode(s) for carrying out the Invention
The invention is based on the observation that the separated aqueous phase contains catalyst which is still active. This has led the current inventors to the insight that reusing at least part of the separated aqueous phase comprising the catalyst, leads to a more efficient use of the catalyst, and lower energy consumption in subsequent separating steps. The combination of a well dispersed biphasic reaction system and reuse of the aqueous phase may lead to a high turn over number, (TON), which is the number of moles of terminal olefin a mole of catalyst can convert before becoming inactivated. Said combination may further lead to a minimized energy consumption for subsequent separation and purification steps, high selectivity towards product for all raw materials and effective usage of reactor volume leading to a less complicated process. The invention is hereafter discussed in greater detail.
The process is carried out in a multiphasic system of an aqueous phase and at least one organic phase. The oxidation (step a)) of the terminal olefin is believed to take place in an aqueous phase, whereas the organic phase is believed to extract or strip produced 1 ,2-epoxide from the water phase. The inventors have found that the organic phase contains little or no water soluble byproducts and catalyst. It is beneficial to use a terminal olefin which has limited solubility in water, for example, allyl chloride and allyl acetate instead of conventionally used allyl alcohol. The multiphasic system may be created by adding the terminal olefin with limited solubility to an aqueous phase in an amount greater than what dissolves in the aqueous phase. Preferred terminal olefins have a maximum solubility of about 100 g/L (at 20°C), more preferably of from 0.01 to 100 g/L.
The volumetric ratio of the organic phase to the aqueous phase, both inside the reactor, and the degree of contact between the phases are important parameters in the performance of the catalyst system. If the amount of organic phase is too high, the aqueous phase is no longer the continuous phase. In this case, there may be insufficient mixing of the ingredients. This means that the conversion rate of terminal olefin is considerably lowered. On the other hand, if the aqueous phase inside the reactor is too high with respect to the amount of organic phase, the terminal olefin concentration in the aqueous phase will be too low with respect to oxidant concentration. This may lead to the production of undesirable side products and catalyst deactivation. Therefore the volumetric ratio of aqueous phase to organic phase inside the reactor is preferably in the range of from 10:1 to 1 :5, with emulsion formation as a maximum limit.
The above limitations can also be influenced by the degree of mixing. In practice this means that the organic phase needs to be well dispersed into the continuous aqueous phase, such as in the form of droplets, preferably as small as possible, for example, less than 3 mm.
Upon dispersion of the organic phase into the aqueous phase, the reaction (catalytic oxidation) of the terminal olefin and the oxidant in the presence of the catalyst may occur (step a)). The resulting reaction mixture is discharged from the reactor. The discharged reaction mixture comprises both product and unreacted starting material. The discharged reaction mixture is allowed to settle into its separate phases, the aqueous phase and the at least one organic phase. The at least one organic phase may comprise two organic phases, such as one dispose below and one disposed above the aqueous phase.
The current inventors surprisingly found that the aqueous phase contains catalyst which is still active. The catalyst contained within the separated aqueous phase, can be reused, thereby increasing the catalyst efficiency.
It is believed to be beneficial that the aqueous phase contains at least trace amounts of the terminal olefin. Without being bound to any theory, it is believed that the presence of terminal olefin allows the catalyst to remain active, whereas it is believed that without the presence of terminal olefin and/or due to the presence of the epoxide and/or oxidant without terminal olefin present the activity of the active catalyst reduces. Cooling may also be used to reduce the decrease in catalyst efficiency.
The aqueous phase can be reused by feeding at least a portion (part) of the separated aqueous phase to a next reactor or by recycling at least a portion of the separated aqueous phase to the same reactor (step d)). Preferably, the at least a portion of the aqueous phase is recycled into the reaction mixture. This way, catalyst present in the recycled aqueous phase is not discharged, but efficiently used again.
When the process is running, per unit time, certain volumes of aqueous starting materials, such as the oxidant, catalyst and, if needed, buffer, are supplied to the reaction mixture (step a)).
These aqueous starting materials are indicated as the aqueous components. Simultaneously, per unit time, also a certain volume of separated aqueous phase is recycled into the reaction mixture. The mass ratio of the volume of aqueous components to the volume of recycled aqueous phase added to the reaction mixture at every instant is indicated as the water recycle ratio. In order to achieve the advantageous effects of recycling the catalyst, said water recycle ratio preferably is in the range of from 10:1 to 1 :10, more preferably of from 2:1 to 1 :5 and most preferably 1 :3.5. Also, turbulent conditions such as a high velocity of the aqueous phase will prevent agglomeration of the organic droplets dispersed in said medium.
The molar ratio of terminal olefin to oxidant is very important in the process of the current invention. The molar ratio of terminal olefin to oxidant may be greater than 1 :2. Preferably, this ratio is in the range of from 12:1 to 1:1. More preferably, this ratio may be 1 :1, 1.2:1, 2:1, or 4:1, or 2:1 to 12:1. If too much oxidant is used, then the selectivity towards the 1,2-epoxide reduces due to the production of undesirable side-products. Another consequence of too much oxidant with respect to terminal olefin is rapid catalyst deactivation. If not enough oxidant is used, then the turnover number is suboptimal. This is therefore significantly different from bleaching conditions described in the prior art, where excessive amounts of oxidant, i.e. hydrogen peroxide are used. To ensure optimal peroxide efficiency, the oxidant is preferably added to the aqueous phase at a rate about equal to the reaction rate of the catalytic oxidation.
The reaction (catalytic oxidation) is carried out using hydrogen peroxide, or a precursor thereof, as an oxidant. Hydrogen peroxide has strong oxidizing properties. It is typically used in an aqueous solution. The concentration of hydrogen peroxide may vary, from 15% (e.g., consumer grade for bleaching hair) to 98% (propellant grade), with a preference for industrial grades varying from 30 to 70%. More preferably, the concentration of hydrogen peroxide is 70%. Other oxidants that may be used include organic peroxides, peracids, and combinations thereof.
The reaction (catalytic oxidation) of the terminal olefin takes place in the aqueous phase. The aqueous phase may have a pH from 1 to 8, such as from 2 to 5. The aqueous phase may further comprise a buffer system to stabilize the pH in a certain range. For instance, it has been found advantageous that the aqueous phase is stabilized in a pH range of from 1 to 8, more preferably of from 2 to 5. The pH is therefore (well) below that used when bleaching olefins with hydrogen peroxide as the oxidant, typically carried out at more alkaline conditions (e.g., pH adjusted with NaHC03 to 9.0). The suitable or preferred range may be achieved by several known acid-salt combinations, with the preferred combination being based on oxalic acid-oxalate salt, acetic acid-acetate salt, malonic acid-malonate salt, and combinations thereof.
The aqueous phase may further comprise minor amounts, if any, of other organic compounds. The aqueous phase may also contain minor amounts of co-solvents, e.g. to increase the solubility of the olefin. Suitable co-solvents include, for example, acetone, methanol, and other water-soluble alcohols. Co-solvents may be used in amounts such as to keep a biphasic system, preferably in an amount < 10 weight percent.
The aqueous phase may further comprise a phase transfer agent and/or a surfactant, in particular if a terminal olefin is used with low solubility (e.g., below 0,1 g/L water). Known phase transfer agents that may be used in the process of the invention include quaternary alkyl ammonium salts. Known surfactants that may be used in the process of the invention include non ionic surfactants such as Triton XI 00™ available from Union Carbide.
The catalyst system comprising a water soluble manganese complex is described as follows. The oxidation catalyst is a water soluble manganese complex. Advantageously, the manganese complexes include mononuclear species of the general formula (I):
[LMnX3]Y (I),
and binuclear species of the general formula (II):
[LMnfo-X)3MnL](Y)„ (II), wherein Mn is a manganese; L or each L independently is a polydentate ligand, preferably a cyclic or acyclic compound containing 3 nitrogen atoms; each X is independently a coordinating species and each μ-Χ is independently a bridging coordinating species, selected from the group consisting of: RO", CI", Br", Γ, F", NCS", N3 ", I3 ", NH3, NR3, RCOO", RS03 ", RS04 ", OH", O2', 02 2", HOO", H20, SH", CN", OCN", and S4 2" and combinations thereof, wherein R is a Ci-C20 radical selected from the group consisting of alkyl, cycloalkyl, aryl, benzyl and combinations thereof, and Y is a non-coordinating counter ion selected from the group consisting of RO", CI", Br", Γ, F", S04 2", RCOO", PF6 ", acetate, tosylate, triflate (CF3S03 " ) and a combination thereof with R once again being a d to C20 radical selected from the group consisting of alkyl, cycloalkyl, aryl, benzyl and combination thereof. The non- coordinating counter ion Y may provide for the charge neutrality of the complex and the value of n depends upon the charge of the cationic complex and anionic counter ion Y, for example, n may be 1 or 2. In one embodiment, an ion of CH3COO" or PF " may be used as the non- coordinating counter ion. Ligands which are suitable for the present invention are acyclic compounds containing at least 7 atoms in the backbone or cyclic compounds containing at least 9 atoms in the ring, each having the nitrogen atoms separated by at least two carbon atoms. A preferred class of ligands is that based on (substituted) triazacyclononane ("Tacn"). The preferred ligand is l,4,7-trimethyl-l,4,7,-triazacyclononane ("TmTacn").
Dinuclear manganese complexes are denoted as preferred, because of their greater activity and solubility in water. Preferred dinuclear manganese complexes are those of the formula [ΜηΓν 2(μ-0)3ί2](Υ)η (same as formula: [LMn^-0)3MnL](Y)n), wherein n is 2, and L and Y have the meaning identified above, preferably TmTacn as ligand, and PF6 " or acetate (CH3C02 ", hereinafter OAc) as counterion.The catalyst system comprising a water soluble manganese complex is described above. The preferred complex for the current invention comprises l,4,7-trimethyl-l,4,7,-triazacyclononane ("TmTacn") as the preferred ligand or ligands. This ligand is commercially available from Aldrich.
The manganese complex is used in catalytically effective amounts. Typically, the catalyst is used in a molar ratio of catalyst (Mn) to the oxidant of from 1 :10 to 1 :10,000,000, preferably of from 1 :100 to 1 :1,000,000, most preferably of from 1 :1000 to 1 :100,000. As a matter of convenience the amount of catalyst may also be expressed in terms of its concentration, when keeping in mind the volume of the aqueous medium. For instance, it may be used in a molar concentration (based on the Mn) of from 0.001 to 10 mmol/L, preferred of from 0.01 to 7 mmol/L and most preferably of from 0.01 to 2 mmol/L.
The reaction conditions for the catalytic oxidation may be quickly determined by a person skilled in the art. The reaction is exothermic, and cooling of the reaction mixture may be required. The reaction is preferably carried out at temperatures anywhere from -5°C to 40°C, dependent upon such physical parameters as melting and boiling point of the used terminal olefins.
According to the invention, the terminal olefin used is an epoxidizible olefin which may be functionalized. The terminal olefin may be a liquid under process conditions, e.g., allyl chloride or liquefied propylene, but also a gas, e.g. gaseous propylene.
Examples of suitable terminal olefins include terminal olefinically unsaturated compounds. In one embodiment, the terminal olefinically unsaturated compound may have at least one unsaturated -C=C- bond, such as at least one unsaturated -C=CH2 group. The olefinically unsaturated compound may comprise more than one unsaturated— C=C- bond. Moreover, the unsaturated -C=C- bond need not be a terminal group. Terminally olefinically unsaturated compounds may have one or more terminal -C=CH2 bonds.
Suitable examples of terminal olefinically unsaturated compounds therefore include the following compounds:
R-CH=CH2
R'-(CH=CH2)n
X-CH=CH2
Y-(CH=CH2)2
wherein R is a radical of 1 or more carbon atoms optionally comprising 1 or more heteroatoms (such as oxygen, nitrogen or silicon); R' is a multivalent radical of 1 or more carbon atoms optionally comprising 1 or more heteroatoms wherein n corresponds with the valence of the multivalent radical; X is a halogen atom, and Y is an oxygen atom.
Of particular interest are olefinically unsaturated compounds selected from the compounds:
(a) vinylchloride or allylchloride; (b) 1-alkene, preferably propene:
(c) mono-, di- or polyallyl ethers of mono-, di- or polyols;
(d) mono-, di- or polyvinyl ethers of mono-, di- or polyols;
(e) mono-, di- or polyallyl esters of mono-, di- or polyacid;
(f) mono-, di- or polyvinyl esters of mono-, di- or polyacids;
(g) divinylether or diallylether.
The terminal olefin may have limited solubility in water, for example, the terminal olefin may have a maximum solubility in the aqueous phase at 20°C of about 100 g/L, more preferably of from 0.01 to 100 g/L at 20°C.
In a more preferred embodiment of the present invention, the terminal olefin is selected from allyl bromide, allyl chloride and allyl acetate. In a most preferred embodiment of the invention allyl chloride is used for the manufacture of epichlorohydrin, because of the commercial interest and ease of isolating the produced epichlorohydrin.
According to another preferred embodiment of the present invention the terminal olefin is propylene in order to produce propylene oxide, and the reaction is carried out at temperatures in the range from -5°C to 40°C. Propylene is preferably used in excess over the oxidant.
According to still another embodiment of the invention, the buffer, if any, and oxidation catalyst are fed as a pre-mixed mixture into step a).
Another aspect of the invention is related to a device carrying out the above process for the manufacture of 1,2-epoxide. According to the invention, the device comprises a reactor for performing the catalytic oxidation having an inlet for feeding the oxidant, the oxidation catalyst, optionally a buffer and the terminal olefin to the reactor, and an outlet for discharging the reaction mixture from said reactor, separating means connected to the reactor outlet for separating the reaction mixture into the at least one organic phase and an aqueous phase, recycling means for recycling part of the aqueous phase separated in the separating means, dispersing means for dispersing the terminal olefin into the aqueous phase and cooling means for controlling the temperature of the catalytic oxidation process. According to the invention, the device comprises a reactor for carrying out the process having an inlet and an outlet. Via the reactor inlet the reactants are fed to the reactor, whereas via the reactor outlet the reaction mixture is discharged. The device further comprises separating means connected to the reactor outlet for separating the reaction mixture into the at least one organic phase and the aqueous phase as explained above. Preferably, this separation means comprises a straight forward liquid to liquid separator, such as a settling tank, since the product forms at least one separate organic phase which phase separates from the aqueous phase when allowed to settle. Other devices such as hydrocyclones can also be used.
The aqueous phase is recycled into the reactor via the inlet of the reactor. This recycling means may be of simple design, e.g. a pipe connecting an aqueous phase outlet of the separation means and the reactor inlet equipped with a pump to transport the aqueous phase into the reactor. It is noted here that the skilled person will be aware that the reactor according to the invention is equipped with standard process technological elements like e.g. pumps, valves and control mechanisms.
The reactor according to the invention further comprises dispersing means for dispersing the organic terminal olefin phase into the aqueous phase and cooling means for controlling the temperature of the catalytic oxidation, because of its exothermic nature.
About the reactor type, several reactor designs are suited to carry out the process according to the invention. The reactor may be a plug flow reactor (PFR). Due to the required high velocity for dispersing and the long residence times a PFR used in the present invention will be a very long PFR. The reactor may also be a continuous stirred tank reactor (CSTR). When using a CSTR, special care should be taken in dispersing the terminal olefin into the aqueous phase.
According to a preferred embodiment of the invention, the catalytic oxidation may also be carried out in a loop reactor. In a loop reactor, the reaction mixture is circulated. When the circulation rate of the loop reactor is about 15 times the rate at which the aqueous components and the terminal olefin is fed, i.e. the feed rate, the loop reactor can be described as a CSTR because of the high degree of back mixing. The advantage of using a loop reactor in the present process is that it allows for the well defined mixing behaviour of a pumped system combined with dispersing means in a compact reactor design. According to yet another preferred embodiment of the invention the dispersing means is a static mixer, since this mixer will provide maximum break up of organic droplets in the continuous aqueous phase.
According to another embodiment of the invention fresh oxidant and olefin are fed to the aqueous phase in subdivided portions to the reactor through multiple inlet parts distributed over the reactor housing.
The present invention is further explained by means of FIG. 1, which shows a schematic representation of an embodiment of a device for the manufacture of epichlorohydrin.
It is noted here that the skilled person facing the task of constructing the device for carrying out the process according to the invention, will be aware that all process technological elements of the device are constructed and operated by using common general process technological knowledge.
In this embodiment, the device 10 comprises a loop reactor 20 comprising an inlet 21 and an outlet 22. Hydrogen peroxide, a water soluble manganese complex as the oxidation catalyst, an oxalate buffer solution and allyl chloride, which are disposed in separate feeding tanks 15, are fed to the reactor 20. The reactants are transported from the feeding tanks 15 to the reactor inlet 21 through feeding conduits 11 by means of feeding pumps 12. A pre-mixing means 50 may be disposed between the inlet 21 and one or more of the feeding pumps 12 to pre-mix some of the components, such as the catalyst and oxalate buffer in FIG 1. The reactor inlet 21 advantageously comprises several inlet ports, one port for each reactant. The reaction mixture is discharged from the reactor 20 via the reactor outlet 22 into a separating means 30. The reactor outlet 22 and separating means 30 are connected via a discharge conduit 13. The separating means 30 comprises a separation inlet 31 through which the reaction mixture is supplied to the separating means 30. In the separating means 30 the at least one organic phase and the aqueous phase are allowed to phase separate. The organic phase comprising epichlorohydrin is isolated from the separating means 30 through the product outlet 32. At least part of the aqueous phase in the separating means 30 is recycled to the reactor 20 via a recycling conduit 41 connecting a recycling outlet 33 of separating means 30 and reactor inlet 21. A recycling pump 42 is comprised in the recycling conduit 41 to transport the aqueous phase. The organic phase inside the reactor 20 is dispersed in the aqueous phase using a dispersing means 23. The reactor 20 further comprises a reactor pump 26 for transporting the reaction mixture and cooling means 24 to cool the reaction mixture. Said cooling means 24 may be e.g. a water cooler or other types of heat exchanging means. However, the choice of the type of cooling means 24 is left to the expertise of the skilled person.

Claims

Claims
1. A process for the manufacture of an epoxide, comprising:
a) adding an oxidant, a water-soluble manganese complex, and a terminal olefin to form a multiphasic reaction mixture, wherein the water-soluble manganese complex is a mononuclear species of the general formula (I):
[LMnX3]Y (I)
or a binuclear species of the general formula (II):
[ίΜη(μ-Χ)3Μηί](Υ)η (II)
wherein Mn is a manganese; L or each L independently is a polydentate ligand, each X independently is a coordinating species and each μ-Χ independently is a bridging coordinating species, and wherein Y is a non-coordinating counter ion;
b) reacting the terminal olefin with the oxidant in the multiphasic reaction mixture having at least one organic phase in the presence of the water-soluble manganese complex; c) separating the reaction mixture into the at least one organic phase and an aqueous phase; and
d) reusing at least part of the aqueous phase.
2. The process according to claim 1, wherein step a) comprises the sub steps of:
al) adding to the reaction mixture the oxidant and the water-soluble manganese complex as aqueous components; and
a2) dispersing the terminal olefin into the aqueous phase.
3. The process according to claim 1 or 2, wherein the reaction takes place in an aqueous phase of the multiphasic reaction mixture.
4. The process according to one of the preceding claims 1 to 3, wherein at least a portion of the aqueous phase obtained in step c) is recycled into step a).
5. Process according to one of the preceding claims 2-4, wherein the water recycle ratio of aqueous components to reused aqueous phase is in the range of from 10:1 to 1 :10, preferably in the range of from 2:1 to 1 :5.
6. Process according to claim 5, wherein the water recycle ratio is about 1:3.5.
SH EET I NCORPORATED BY REFERENCE (RULE 20.6)
7. The process according to one of the preceding claims 1 to 6, wherein the molar ratio of terminal olefin to oxidant is in the range of from 12:1 to 1 :1.
8. The process according to one of the preceding claims 1 to 7, wherein the terminal olefin has a maximum solubility at 20 °C of about 100 g/L.
9. The process according to one of the preceding claims 1 to 8, wherein the aqueous phase further comprises a buffer system to stabilize the pH in the range of from 1 to 8, and the buffer is added to the reaction mixture as an aqueous component.
10. The process according to one of the preceding claims 1 to 9, wherein the reaction is carried out at temperatures in the range of from -5°C to 40°C.
11. The process according to one of the preceding claims 1 to 10, wherein the terminal olefin is selected from allyl bromide, allyl chloride and allyl acetate and the reaction is carried out at temperatures in the range from -5°C to 40°C.
12. The process according to one of the preceding claims 1 to 11, wherein the terminal olefin is propylene and the reaction is carried out at temperatures in the range from -5°C to 40°C.
13. The process according to one of the preceding claims 1 to 12, wherein the molar ratio of water-soluble manganese complex to oxidant is in the range of from 1 : 10 to 1 : 10,000,000.
14. The process according to one of the preceding claims 1 to 13, wherein the oxidant is hydrogen peroxide or a precursor thereof.
15. Device (10) for carrying out the process of the preceding claims 1 to 14, comprising: a reactor (10) for performing the catalytic oxidation having an inlet (10) for feeding the oxidant, the water-soluble manganese complex, optionally the buffer and the terminal olefin to the reactor (10), and an outlet (22) for discharging the reaction mixture from said reactor (20), separating means (30) connected to the reactor outlet (22) for separating the reaction mixture into the at least one organic phase and the aqueous phase, recycling means (40) for recycling part of the aqueous phase separated in the separating means (30), dispersing means (23) for dispersing the organic phase into the aqueous phase and cooling means (24) for controlling the temperature of the catalytic oxidation process.
16. Device (10) according to claim 15, wherein the reactor (20) is a continuous loop reactor.
17. Device according to claim 15 or 16, wherein the dispersing means (23) is a static mixer.
PCT/EP2011/000320 2010-02-02 2011-01-26 Process for the manufacture of a 1,2-epoxide and a device for carrying out said process Ceased WO2011107188A2 (en)

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EP11702144A EP2539329A2 (en) 2010-02-02 2011-01-26 Process for the manufacture of a 1,2-epoxide and a device for carrying out said process
AU2011223288A AU2011223288B2 (en) 2010-02-02 2011-01-26 Process for the manufacture of a 1,2-epoxide and a device for carrying out said process
KR1020127022622A KR101475579B1 (en) 2010-02-02 2011-01-26 Process for the manufacture of a 1,2-epoxide and a device for carrying out said process
RU2012137285/04A RU2540864C2 (en) 2010-02-02 2011-01-26 Method of producing 1,2-epoxide and apparatus for implementing said method
BR112012019183A BR112012019183A8 (en) 2010-02-02 2011-01-26 PROCESS FOR MANUFACTURING AN EPOXIDE, AND DEVICE FOR CARRYING OUT THE PROCESS
US13/574,715 US8859790B2 (en) 2010-02-02 2011-01-26 Process for the manufacture of a 1,2-epoxide and a device for carrying out said process
JP2012551532A JP6000856B2 (en) 2010-02-02 2011-01-26 Method for producing 1,2-epoxide and apparatus for carrying out the method
KR1020147029535A KR101622504B1 (en) 2010-02-02 2011-01-26 Process for the manufacture of a 1,2-epoxide and a device for carrying out said process
CN201180008055.1A CN102844310B (en) 2010-02-02 2011-01-26 Process for producing 1,2-epoxides and apparatus for carrying out the process
KR1020147008554A KR20140056381A (en) 2010-02-02 2011-01-26 Process for the preparation of 1,2-epoxide and apparatus for carrying out the process
US14/184,412 US9102640B2 (en) 2010-02-02 2014-02-19 Process for the manufacture of a 1,2-epoxide and a device for carrying out said process

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