Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C263/00—Preparation of derivatives of isocyanic acid
  • C07C263/10—Preparation of derivatives of isocyanic acid by reaction of amines with carbonyl halides, e.g. with phosgene

Definitions

• the invention relates to a process for the preparation of isocyanates and / or polyisocyanates by reacting the corresponding amines with phosgene, optionally in the presence of an inert medium, in a reactor, wherein a first educt stream containing the amine is fed to the reactor in liquid form and a phosgene containing second reactant stream is fed to the reactor in gaseous form.
• the production of isocyanates by phosgenation of the corresponding amines can be carried out in principle by a liquid phase or a gas phase phosgenation.
• the gas phase phosgenation is characterized by the fact that a higher selectivity, a lesser hold-up of toxic phosgene and a reduced energy requirement are required.
• a liquid-phase phosgenation is characterized by the fact that the reaction can be carried out at lower temperatures and evaporation of the educts is not required.
• a centrifugal reactor In order to carry out a liquid-phase phosgenation in which a liquid, amine-containing stream and a liquid, phosgene-containing stream react with one another, a centrifugal reactor is described in CN 101 104595 A. In this process, the liquid educt streams are rapidly mixed and reacted. Disadvantage of the liquid phase phosgenation described here, however, is that the yield is low and a higher energy consumption is necessary. In addition, a higher hold-up of phosgene is required.
• the object of the present invention is to provide a process for the preparation of isocyanates and / or polyisocyanates which does not have the disadvantages known from the prior art.
• the object is achieved by a process for the preparation of isocyanates and / or polyisocyanates by reacting the corresponding amines with phosgene, optionally in the presence of an inert medium, in a reactor, wherein a first educt stream containing the amine is fed to the liquid and a liquid containing the phosgene second reactant stream is supplied to the reactor gaseous, wherein the reactor is a centrifugal reactor having a rotating about a central axis pack in a housing, wherein the first reactant stream and the second reactant stream of the rotating packing are fed so that the educt streams due to the centrifugal force in the pack are mixed and transported to the outside, wherein the phosgene reacts with the amine to the corresponding isocyanate or polyisocyanate by mixing in the pack.
• the process according to the invention first combines the advantages of gas phase phosgenation and liquid phase phosgenation.
• the reaction can be carried out at lower temperatures than gas phase phosgenation. This also makes it possible to phosgenate amines that are not accessible to the gas phase phosgenation.
• the formation of by-products can be reduced by the method according to the invention.
• centrifugal reactor also has the advantage that no aerosol droplets must be formed, which have to be removed from the gas stream again after the reaction has been carried out. This also the disadvantages of the known gas / liquid phosgenation, as described for example in WO-A 2008/006775, avoided.
• the separation of the gas phase from the liquid phase occurs at the exit from the rotating packing due to the centrifugal force.
• Another advantage of the method according to the invention is that very short residence times are achieved with the centrifugal reactor, which leads to minimal yield losses and high product qualities.
• High product quality in this context means a product having a good color number, low chlorine content, high NCO numbers, an optimum molecular weight distribution, etc.
• the reaction is preferably carried out at a pressure in the range from 1 to 20 bar (absolute), preferably in the range from 1 to 10 bar (absolute) and more preferably in the range from 1 to 5 bar (absolute).
• the temperature is preferably in the range of 50 to 400 ° C, more preferably in the range of 100 to 300 ° C and particularly preferably in the range of 150 to 250 ° C.
• the centrifugal reactor is preferably operated in such a way that A centrifugal acceleration of from 1 to 5000 g, more preferably a centrifugal acceleration in the range of 10 to 1000 g, and particularly preferably a centrifugal acceleration in the range of 50 to 250 g, where g is the gravitational acceleration with a value of 9.81 m / s 2 is.
• unreacted phosgene can - possibly after a purification - lead back and use for phosgenation.
• Hydrogen chloride formed in the reaction may also be optionally used after purification, for the production of vinyl chloride or for the production of hydrochloric acid.
• amines which are reacted with the process according to the invention for the preparation of isocyanates
• customary amines can be used. These are, for example, aliphatic diamines such as hexamethylenediamine (HDA), isophoronediamine (IPDA), and toluenediamine (TDA) and methylenedi (phenyldiamine) (MDA) in a mixture with its higher homologs.
• HDA hexamethylenediamine
• IPDA isophoronediamine
• TDA toluenediamine
• MDA methylenedi (phenyldiamine)
• the inventive method can be used particularly advantageously.
• 4,4'-MDA is used. This is generally in a mixture with its isomeric compounds 2,2'-MDA and 2,4'-MDA.
• the first reactant stream containing the amine additionally contains at least one solvent.
• solvents are used which are inert before, during and after the reaction of the amines with the phosgene. Suitable solvents are, for example, organic solvents, for example aromatic solvents, which may also be halogenated.
• Suitable solvents are, for example, toluene, monochlorobenzene, o- or p-dichlorobenzene, trichlorobenzene, chlorotoluene, chloroylol, chloroethylbenzene, chloronaphthalene, chlorodiphenyl, xylene, decahydronaphthalene, benzene and mixtures thereof.
• Other suitable organic solvents are, for example, methylene chloride, perchlorethylene, hexane, diethyl isophthalate, tetrahydrofuran (THF), dioxane, trichlorofluoromethane, butyl acetate and dimethylformamide (DMF).
• the viscosity of the liquid containing the amine first reactant stream can be reduced and thereby a smaller film thickness can be produced. This allows a faster mixing of the amine-containing liquid educt stream with the phosgene.
• the liquid flows through the reactor at the same speed at a higher speed, whereby the residence time can be further reduced.
• the phosgene is preferably added in excess based on the amine groups.
• the molar ratio of phosgene to amine groups is preferably from 1.01: 1 to 6: 1, more preferably from 1.1: 1 to 4: 1, and particularly preferably from 1.2: 1 to 3: 1.
• a centrifugal reactor used according to the invention for carrying out the process usually has a first feed for the first feed stream and a second feed for the second feed stream, wherein both the first feed stream of the pack via the first feed and the second feed stream of the pack via the second feed supplied centrally become.
• the central feed ensures that the entire radial extent of the packing can be utilized for the mixing of liquid educt stream and gaseous educt stream and thus for carrying out the reaction.
• the central feed ensures that the liquid in the pack is maximally accelerated.
• the supply of the first educt stream and the second educt stream can be effected via two separate feeds, which are designed, for example, in the form of pipelines, respectively.
• two concentric tubes wherein the liquid first feed stream and through the outer tube of the gaseous second reactant stream are supplied through the inner tube.
• the first liquid reactant stream is fed through the inner tube of the gaseous second educt current and the outer tube.
• the package has channels through which liquid and gas can flow. Due to the rotation of the package, a liquid film forms on the walls of the channels formed in the package.
• the packing of the centrifugal reactor can be structured or unstructured. In the pack, the mixing of the liquid and the gaseous phase takes place.
• the gas phase is preferably continuous.
• a film flow forms, wherein liquid flows as a film on the surfaces of the pack and the gas flows through the free volumes of the channels.
• the outlet of the pack that is to say at the outer periphery of the pack, there is a drop flow at which the liquid emerges from the pack in the form of drops. The droplets move in the gas phase, which also leaves the reactor.
• the channels in the package are designed such that the package is porous and has a specific surface area of more than 200 m 2 / m 3 .
• a large area is achieved on which the liquid can form as a film and thus a high throughput is made possible.
• a porous packing allows a more uniform wetting of the surfaces and thus a more uniform reaction.
• Suitable materials for the pack are, for example, metals or ceramics. These are sufficiently resistant to the temperatures occurring during the reaction.
• the rotating packing of the centrifugal reactor may be constructed, for example, of disordered fibers or of a ball-bed. However, packages in the form of packed beds are also possible. As filler any other shaped body can be used. As a shaped body, for example, cylinders, rings or Berls decisivtel are.
• the rotating packing can also be designed in the form of structured internals, for example as a static mixer or monolith or in any other form. Another possibility is the use of open-celled foams.
• the rotating pack is housed in a fixed housing.
• the droplets leaving the pack are thrown outwards due to the centrifugal force and collide against the housing.
• a liquid film forms on the wall of the housing, which flows downwards due to gravity.
• the liquid is collected and can be removed via a liquid discharge from the housing.
• the liquid is collected on the housing bottom and discharged through a liquid outlet.
• the gas is preferably removed from the housing at the top of the housing. As a result, a separation into gas and liquid is already achieved in the reactor.
• the reactor additionally comprises an inert gas inlet.
• an inert gas can be supplied to the reactor. This allows the reactor to be purged with, for example, an inert gas before the reactor is put into operation.
• the inert gas is also preferably removed via the gas outlet, over which during operation the gaseous unreacted phosgene and the hydrogen chloride produced in the reaction is withdrawn.
• the liquid product stream which is withdrawn from the reactor usually contains the isocyanate prepared, optionally used solvent and low Quantities of by-products.
• the by-products remaining in the isocyanate can be separated from isocyanate, for example, by additional rectification or crystallization in a step subsequent to the reaction.
• An embodiment of the invention is shown in the figure and will be explained in more detail in the following description.
• the single FIGURE shows a schematic representation of a centrifugal reactor used for the preparation of isocyanates.
• a centrifugal reactor 1 is fed via a first inlet 3, a first amine-containing reactant stream.
• a second phosgene-containing, gaseous educt stream is fed via a second feed 5.
• the first inlet 3 and the second inlet 5 are arranged such that they open in a package 9 rotating about a central axis 7. From the first inlet 3 and the second inlet 5 enter the educt streams in the rotating packing 9.
• channels are formed, on the walls of which due to the rotation of the rotating packing 9 and the associated centrifugal force of the liquid first Eduktstrom applies. On the walls of the rotating packing 9 is formed in this way a thin liquid film, which comes into contact with the phosgene of the second reactant stream.
• the phosgene reacts with the amine in the liquid to form isocyanate.
• the rotating package 9 may be formed as an ordered or disordered package.
• the rotating packing 9 in the form of a cage which is filled with filling material, for example random packings.
• the packing for example, from fibers or balls, wherein it is preferred in a production of balls to sinter them into a compact package, wherein between the individual balls, the channels are formed.
• the rotating packing 9 is particularly preferred to design the rotating packing 9 as a porous packing with a specific surface area of more than 200 m 2 / m 3 . This large specific surface leads to a correspondingly good liquid distribution within the rotating packing 9 and thus to a low film thickness of the liquid on the wall. fertilize the pack. Due to the low film thickness of the mass transfer is further improved with the gaseous second reactant stream.
• the rotational speed of the rotating packing 9 is preferably in the range of 50 to 10,000 min -1 .
• the housing furthermore has a gas inlet 23.
• the rotating packing 9 it is also possible to enclose the rotating packing 9 with a ring within the housing 13, wherein the ring is designed as a baffle ring, against which the drops of the rotating packing 9 tearing drops. At the baffle ring, the drops are deflected and directed to the bottom of the housing 13, so that the liquid can be removed from the centrifugal reactor 1 via the liquid outlet 19.
• the maximum speed of the package is preferably selected so that the tearing drops have a size that allows for easy separation by impacting the housing wall or ring.
• the liquid removed via the outlet 19 can be worked up in a subsequent step.
• liquid or solid reaction by-products can be removed from the desired reaction product, namely the isocyanate.
• the gas removed via the gas outlet 21, which is shown here with an arrow 25, can also be processed.
• the hydrogen chloride can be used via the detour of the chlorine synthesis for the production of phosgene or alternatively also for hydrochloric acid production or vinyl chloride production.
• the process according to the invention is particularly suitable for carrying out the amine phosgenation for the preparation of isocyanates for amines which can not be evaporated or which have a very high evaporation temperature.
• the process according to the invention is particularly suitable for the phosgenation of MDA or polymeric MDA for the preparation of the respectively corresponding isocyanates or polyisocyanates.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

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Cited By (10)

Citations (3)

• 2011
  • 2011-10-27 EP EP11186815.4A patent/EP2586770A1/de not_active Ceased
• 2012
  • 2012-10-26 IN IN3051CHN2014 patent/IN2014CN03051A/en unknown
  • 2012-10-26 EP EP12777924.7A patent/EP2771314A1/de not_active Withdrawn
  • 2012-10-26 WO PCT/EP2012/071251 patent/WO2013060836A1/de not_active Ceased
  • 2012-10-26 JP JP2014537628A patent/JP2015501313A/ja not_active Withdrawn
  • 2012-10-26 CN CN201280052284.8A patent/CN103889949A/zh active Pending
  • 2012-10-26 KR KR1020147013854A patent/KR20140093243A/ko not_active Withdrawn
  • 2012-10-26 BR BR112014010012A patent/BR112014010012A2/pt not_active IP Right Cessation

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