[go: up one dir, main page]

WO2013030172A1 - Procédé de régénération de catalyseurs de raney - Google Patents

Procédé de régénération de catalyseurs de raney Download PDF

Info

Publication number
WO2013030172A1
WO2013030172A1 PCT/EP2012/066640 EP2012066640W WO2013030172A1 WO 2013030172 A1 WO2013030172 A1 WO 2013030172A1 EP 2012066640 W EP2012066640 W EP 2012066640W WO 2013030172 A1 WO2013030172 A1 WO 2013030172A1
Authority
WO
WIPO (PCT)
Prior art keywords
eddn
edmn
water
reactor
reaction
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.)
Ceased
Application number
PCT/EP2012/066640
Other languages
German (de)
English (en)
Inventor
Hermann Luyken
Sebastian Ahrens
Gordon Brasche
Jens Baldamus
Robert Baumann
Randolf Hugo
Stephanie JAEGLI
Johann-Peter Melder
Jörg PASTRE
Boris Buschhaus
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.)
BASF SE
Original Assignee
BASF SE
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
Application filed by BASF SE filed Critical BASF SE
Publication of WO2013030172A1 publication Critical patent/WO2013030172A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/74—Iron group metals
    • B01J23/75—Cobalt
    • 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
    • B01J25/00—Catalysts of the Raney type
    • B01J25/02—Raney nickel
    • 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
    • B01J25/00—Catalysts of the Raney type
    • B01J25/04—Regeneration or reactivation
    • 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
    • B01J38/00—Regeneration or reactivation of catalysts, in general
    • B01J38/04—Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst
    • B01J38/08—Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst using ammonia or derivatives thereof
    • 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
    • B01J38/00—Regeneration or reactivation of catalysts, in general
    • B01J38/04—Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst
    • B01J38/10—Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst using elemental hydrogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/44—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers
    • C07C209/48—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers by reduction of nitriles
    • 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
    • Y02P20/584—Recycling of catalysts

Definitions

  • the present invention relates to a process for the regeneration of Raney catalysts.
  • Another object of the present invention is the preparation of amines by hydrogenation of nitriles, wherein the hydrogenation is carried out in the presence of a catalyst regenerated according to the invention.
  • Another object of the present invention is the preparation of epoxy resins, amides or polyamides from the inventively obtained DETA or TETA. It is known from EP 892777 to regenerate Raney cobalt at temperatures of 150 to 400 ° C. and pressures of 0.1 to 30 MPa for 2 to 48 hours with hydrogen, it being advantageous to regenerate the catalyst with the catalyst before the actual regeneration to wash the solvent contained in the system, in particular with ammonia.
  • WO 99/33561 discloses a process for the regeneration of Raney catalysts, wherein initially the separation of the catalysts from the reaction medium takes place and the separated catalyst is treated with a basic solution having a concentration of basic ions of more than 0.01 mol / kg and keeps the mixture at temperatures of less than 130 ° C for 1 to 10 hours, optionally in the presence of hydrogen. Subsequently, the catalyst is washed with water or a basic solution until the wash water has a pH in the range from 12 to 13.
  • WO 2008/104553 discloses that catalysts which are used for the hydrogenation of TETA or DETA can be regenerated according to WO 99/33561.
  • the object of the present invention was to provide a process for the regeneration of Raney cobalt catalysts available.
  • the regeneration should be made possible with simple technical means.
  • the regeneration should be carried out with as little time as possible in order to reduce breastfeeding as a result of catalyst regeneration.
  • the regeneration should allow for the most complete recovery of the activity of the catalysts used.
  • the catalysts regenerated according to the invention should be able to be used in the hydrogenation of nitriles, in particular of thermally labile nitriles of the formula (I), especially EDDN or EDMN.
  • the proportion of undesirable side reactions in the hydrogenation of said nitriles for example AEPIP from the hydrogenation of EDDN or EDMN should be reduced.
  • the task was solved by a
  • a process for the regeneration of Raney catalysts wherein the catalyst with liquid ammonia having a water content of less than 5 wt.% And hydrogen at a partial pressure of 0.1 to 40 MPa in the temperature range of 50 to 350 ° C at least
  • Raney catalysts are regenerated.
  • So-called skeletal catalysts which are also referred to as catalysts of the Raney® type (hereinafter also: Raney catalyst), are obtained by leaching (activation) of an alloy of hydrogenation-active metal and a further component (preferably Al).
  • the catalysts may additionally contain one or more promoters.
  • Raney cobalt or Raney nickel catalysts are used in the process, particularly preferably Raney cobalt and / or Raney nickel catalysts with at least one of Elements Cr, Ni or Fe doped Raney cobalt or with one of the elements Mo, Cr or Fe doped Raney nickel catalysts used.
  • the Raney catalysts used are preferably prepared starting from an alloy of cobalt or nickel, more preferably cobalt, and another alloying component which is soluble in alkalis.
  • this soluble alloy component aluminum is preferably used, but other components such as zinc and silicon or mixtures of such components may be used.
  • the soluble alloying component is wholly or partly extracted with alkali, for which example aqueous sodium hydroxide solution can be used.
  • alkali for which example aqueous sodium hydroxide solution can be used.
  • the catalyst can then z. B. be washed with water or organic solvents.
  • the activation of the catalysts by leaching the soluble component can either be in the reactor itself or before it is charged to the reactor.
  • the preactivated catalysts are sensitive to air and pyrophoric and are therefore usually under a medium such.
  • a medium such as water, an organic solvent or a substance that is present in the subsequent hydrogenation (solvent, educt, product) stored and handled or embedded in an organic compound which is solid at room temperature.
  • the activation is z. As described in EP-A 1 209 146.
  • a Raney cobalt skeletal catalyst which was obtained from a Co / Al alloy by leaching with aqueous alkali metal hydroxide solution, for example sodium hydroxide, and subsequent washing with water, and preferably as promoters of at least one of the elements Contains Fe, Ni or Cr.
  • promoters are metals of subgroups IB, VIB and / or VIII of the Periodic Table, such as chromium, iron, molybdenum, nickel, copper, etc.
  • Such preferred Raney co-catalysts typically contain, in addition to cobalt, 1 to 30% by weight Al, especially 2 to 12% by weight Al, very particularly 3 to 6% by weight Al, 0 to 10% by weight Cr , especially 0.1-7 wt.% Cr, especially 0.5-5 wt.% Cr, in particular 1.5- 3.5 wt.% Cr, 0-10 wt.% Fe, especially 0.1 to 3 wt.% Fe, more particularly 0.2 to 1 wt.% Fe, and / or 0 to 10 wt.% Ni, especially 0.1 to 7 wt.% Ni, especially 0.5 to 5 wt .-% Ni, in particular 1 to 4 wt .-% Ni, wherein the weights are based in each case on the total catalyst weight.
  • a cobalt skeletal catalyst "Raney 2724" from W. R. Grace & Co. can be used as catalyst in the hydrogenation, this catalyst having the following composition:
  • Al 2-6 wt.%, Co:> 86 wt.%, Fe: 0-1 wt.%, Ni: 1-4 wt.%, Cr: 1.5- 3.5 wt. -%.
  • the catalysts can be used as unsupported catalysts or supported.
  • the preferred carriers are metal oxides such as Al 2 O 3, SiO 2, ZrC 2, Z 2, mixtures of metal oxides or carbon (activated carbons, carbon blacks, graphite).
  • the catalysts are used as powder, grit or shaped body (preferably extrudates or tablets).
  • the Raney catalyst particle size is preferably between 0.1 and 500 ⁇ , in particular 1 and 100 ⁇ .
  • the regeneration of the catalyst can be carried out in the actual reactor (in situ) or on the finished catalyst (ex situ). In the case of fixed-bed processes, regeneration is preferably carried out in situ.
  • the entire catalyst is regenerated.
  • the regeneration usually takes place during a short-term shutdown.
  • the Raney catalysts are regenerated, in which the Raney catalysts are treated with liquid ammonia and hydrogen.
  • the should Regeneration can be made with simple technical means.
  • the regeneration should be done with as little time as possible in order to reduce breastfeeding as a result of catalyst regeneration.
  • the regeneration should allow for the most complete recovery of the activity of the catalysts used.
  • the present invention relates to
  • a process for the regeneration of Raney catalysts in which the catalyst with liquid ammonia having a water content of less than 5 wt.% And hydrogen at a partial pressure of 0.1 to 40 MPa in the temperature range of 50 to 200 ° C at least
  • the Raney catalyst is treated with ammonia.
  • the ammonia used in this particularly preferred embodiment contains less than 5 wt .-%, preferably less than 3 wt .-% and most preferably less than 1 wt .-% water.
  • Such "anhydrous" ammonia is a commercially available product.
  • the regeneration can generally be carried out in all reactors in which reactions are carried out with Raney catalysts, in particular those which can be used for the hydrogenation of nitriles, and which are described below and above.
  • the regeneration in a stirred reactor, jet loop reactor, jet nozzle reactor, bubble column reactor, tubular reactor but also Rohbündelreaktor or in a cascade of such identical or different reactors can be performed.
  • the preferred reactor is first emptied prior to treatment with ammonia thereto, for example, by removing the reactor contents from the reactor, e.g. by pumping or draining.
  • the emptying of the reactor should be largely complete.
  • Preferably more than 80% by weight, more preferably more than 90% by weight and most preferably more than 95% by weight of the reactor contents should be drained or pumped off.
  • the liquid ammonia can also originate from condensation reactions within the reactor, for example from the condensation of EDA to AEPIP.
  • the treatment of the catalyst with liquid ammonia is carried out according to the invention at a temperature of 50 to 350 ° C, preferably 150 to 300 ° C, particularly preferably 200 to 250 ° C.
  • the duration of the treatment is at least 0.1 hours, preferably 0.1 to 100 hours, more preferably 0.1 to 10 hours and especially preferably 0.5 to 5 hours.
  • the weight ratio of amount of ammonia fed to catalyst is preferably in the range from 1: 1 to 1000: 1, more preferably in the range from 50: 1 to 200: 1.
  • ammonia is circulated during the treatment with ammonia, for example by pumping over, or preferably by stirring.
  • the treatment of the catalyst with ammonia takes place in the presence of hydrogen.
  • the hydrogen partial pressure in the treatment with ammonia is preferably in the range from 1 to 400 bar, more preferably at 5 to 300 bar.
  • the concentration of anions in the liquid ammonia is less than 0.01 mol / kg, very particularly preferably less than 0.0099 mol / kg and particularly preferably less than 0.005 mol / kg.
  • ammonia can be separated from the catalyst. This is done for example by emptying the reactor and / or stopping the ammonia feed.
  • the Raney catalyst Before and after the treatment of the Raney catalyst with liquid ammonia, the Raney catalyst can be rinsed one or more times with organic solvent and / or water.
  • the treatment of the catalyst with organic solvent and / or water after the separation of ammonia or after termination of the ammonia feed is not absolutely necessary in some reactions, in particular the hydrogenation of nitriles, since the ammonia does not interfere in the course of the subsequent hydrogenation and can be discharged continuously from the reactor.
  • the regeneration is preferably carried out for Raney catalysts used in the hydrogenation of nitriles. Regeneration of Raney catalysts which is particularly useful in the hydrogenation of nitriles of the formula (I) is particularly preferred.
  • R 2 is -NH-CH 2 -CN (I) in which R 2 is hydrogen or radicals of the formula (II)
  • Aminoacetonitrile is accessible by reaction of formaldehyde cyanohydrin (FACH) with ammonia (WO 2008/104578). At higher temperatures, ammonia and FACH or ammonia, formaldehyde and hydrogen cyanide give iminodiacetonitrile (IDAN) (WO 2008/104578).
  • FACH formaldehyde cyanohydrin
  • IDAN iminodiacetonitrile
  • EDDN and / or EDMN is generally prepared by reacting FA, HCN and EDA in the presence of water.
  • EDA EDA can be prepared by the EDC (ethylene dichloride) process by reacting ethylene dichloride (EDC) with aqueous ammonia. Details of the method are given, for example, in Ullmann (Article “Amines, aliphatic” in Ullmann's Encyclopedia of Industrial Chemistry, Karsten Eller, Erhard Henkes, Roland Rossbacher and Hartmut Höke, Published Online: 15 JUN 2000, DOI: 10.1002 / 14356007.a02_001, Page 33).
  • EDA monoethanolamine
  • ammonia article "Amines, aliphatic” in Ullmann's Encyclopedia of Industrial Chemistry, Karsten Eller, Erhard Henkes, Roland Rossbacher and Hartmut Höke, Published Online: 15 JUN 2000, DOI: 10.1002 / 14356007.a02_001, page 33 or Hans-Jürgen Arpe, Industrial Organic Chemistry, 6th edition (2007), Wiley VCH, 2007).
  • EDA can also be obtained by hydrogenation of aminoacetonitrile (AAN), whereby AAN can be prepared by reacting hydrocyanic acid, formaldehyde (FA) and ammonia.
  • AAN aminoacetonitrile
  • FA formaldehyde
  • ammonia ammonia
  • EDA is used in the form of its free base, but if desired, it is also possible to use salts, such as the dihydrochloride of EDA, as starting material.
  • the purity of the EDA used in the process is preferably 95% by weight and more, more preferably 98% by weight and more, most preferably 99% by weight and more, and most preferably 99.5% by weight or more , FA
  • formaldehyde is used as a further starting material.
  • Formaldehyde is a commercially available chemical.
  • formaldehyde is used as a 30 to 50% aqueous solution.
  • hydrocyanic acid is used for the production of EDDN and / or EDMN.
  • Hydrocyanic acid is also a commercially available chemical.
  • Hydrocyanic acid can be produced industrially by essentially three different processes. According to a first method, hydrogen cyanide can be obtained by ammoxidation of methane with oxygen and ammonia (Andrussow method). According to a second method, hydrocyanic acid can be obtained from methane and ammonia by ammondehydrogenation in the absence of oxygen. Finally, hydrocyanic acid can be produced industrially by dehydration of formamide.
  • the hydrocyanic acid produced by these processes is usually added to an acidic stabilizer, for example SO 2, sulfuric acid, phosphoric acid or an organic acid, such as acetic acid, in order to prevent the autocatalytic polymerization of hydrocyanic acid, which can lead to blockages in pipelines.
  • an acidic stabilizer for example SO 2, sulfuric acid, phosphoric acid or an organic acid, such as acetic acid
  • Hydrocyanic acid can be used liquid or gaseous, in pure form or as an aqueous solution.
  • hydrocyanic acid Preference is given to using hydrocyanic acid as 50 to 95% strength by weight, particularly preferably as 75 to 90% strength by weight, aqueous solution.
  • Hydrocyanic acid is preferably used in a purity of more than 90% by weight or more.
  • Stabilizer-free HCN is preferably used.
  • the stabilizer is an organic acid, especially acetic acid.
  • the EDDN preparation is carried out substantially free of cyanogen salts, such as KCN.
  • the reaction of EDA, HCN and FA preferably takes place in the presence of water.
  • HCN and FA In the reaction of EDA, HCN and FA generally 1 mole of water is formed per mole of formaldehyde used. However, water can also be supplied additionally, for example by using the educts in the form of their aqueous solutions. In particular, as described above, FA and / or HCN are generally used as the aqueous solution for the production of EDDN or EDMN.
  • the amount of water used is generally in the range of 1 to 50 moles per mole, preferably in the range of 2 to 40 moles, and more preferably in the range of 3 to 30 moles per mole of EDA used.
  • water is preferably mixed with EDA in a molar ratio of water to EDA of from 1: 1 to 6: 1.
  • Organic solvent The reaction of EDA, HCN and FA preferably takes place in the presence of an organic solvent.
  • Preferred organic solvents are those selected from the group consisting of aliphatic, cycloaliphatic, araliphatic, aromatic hydrocarbons, alcohols and ethers.
  • the organic solvent is stable under the conditions of subsequent hydrogenation of EDDN and / or EDMN.
  • the organic solvent is condensable at a pressure in the range of 50 to 500 mbar in the range of 20 to 50 ° C in order to use normal cooling water in the subsequent workup of EDDN or EDMN for condensing. Furthermore, it is preferred that the organic solvent boils low enough to adjust a bottom temperature of less than 100 ° C in the subsequent water separation during the work-up of the reaction.
  • Preferred organic solvents are, for example, cyclohexane, methylcyclohexane, toluene, N-methylmorpholine, o-xylene, m-xylene or p-xylene, anisole, n-pentane, n-hexane, n-heptane, n-octane, n-nonane , Diisobutyl ether, mineral spirits, gasoline, benzene, diglyme, tetrahydrofuran, 2- and 3-methyltetrahydrofuran (MeTHF) and cyclohexanol, or mixtures of these compounds.
  • cyclohexane methylcyclohexane, toluene, N-methylmorpholine, o-xylene, m-xylene or p-xylene, anisole, n-pentane, n-hexane, n-heptane, n-
  • Particularly preferred solvents are cyclohexane, methylcyclohexane, toluene, N-methylmorpholine, o-xylene, m-xylene or p-xylene, anisole, n-pentane, n-hexane, n-heptane, n-octane, n-nonane, diisobutyl ether, Mineral spirits, gasoline (benzene), diglyme and MeTHF, or mixtures of these compounds.
  • the amount of organic solvent is generally 0.1 to 50 kg per kg, preferably 1 to 30 kg, more preferably 3 to 25 kg per kg of EDA used.
  • an organic solvent is used which has a boiling point which is between water and EDDN or EDMN, in particular under the conditions of the distillative water removal described below. As described below, organic solvents boiling in this region allow for particularly efficient separation of water from the reaction effluent obtained in the reaction of FA, HCN and EDA.
  • Particularly preferred solvents having a boiling point between water and EDDN or EDMN are toluene, N-methylmorpholine, o-xylene, m-xylene or p-xylene, anisole, n-octane, n-nonane, diisobutyl ether and diglyme, or Mixtures thereof.
  • a low-boiling azeotrope corresponds to the ⁇ , ⁇ -diagram
  • Particularly preferred organic solvents having a boiling point which lies between water and EDDN or EDMN and which form a low-boiling azeotrope with water are toluene, N-methylmorpholine, o-xylene, m-xylene or p-xylene, anisole, Octane, n-nonane, diisobutyl ether and diglyme, or mixtures thereof.
  • the organic solvent having a boiling point between water and EDDN and / or EDMN forms a low-boiling azeotrope with water
  • the organic solvent has a miscibility in water, particularly among those Conditions of the following work-up steps described. This facilitates later separation of water and organic solvents.
  • the solubility of such an organic solvent is 1 wt% or less, more preferably 0.5 wt% or less, and most preferably 0.1 wt% or less , In particular, toluene is preferred as such organic solvent.
  • an organic solvent which has a boiling point below the boiling point of water and which forms a low-boiling azeotrope with water, in particular under the conditions of the distillative water separation described below.
  • Particularly preferred solvents which have a boiling point below the boiling point of water and which form a low-boiling azeotrope with water are n-pentane, n-hexane, n-heptane, tetrahydrofuran, cyclohexane, methylcyclohexane, mineral spirits, gasoline (benzene) or mixtures thereof .
  • Such a solvent should preferably have a boiling point of at least 50 ° C. and more preferably of at least 60 ° C. under normal conditions in order to achieve such high condensation temperatures, so that the use of brine on the condenser can be avoided.
  • the solvent used which has a boiling point below the boiling point of water and which forms a low-boiling azeotrope with water, under the conditions prevailing in the reaction of FA, HCN and EDA conditions or the subsequent work-up a low solubility in water or a miscibility with water.
  • the solubility of such an organic solvent in water is 1 wt% or less, more preferably 0.5 wt% or less, and most preferably 0.1 wt% or less.
  • the reaction of EDA, FA and HCN to EDDN and / or EDMN is carried out in the presence of toluene as solvent and the subsequent hydrogenation of EDDN and / or EDMN to TETA and / or DETA is in the presence of THF performed.
  • toluene as solvent
  • the subsequent hydrogenation of EDDN and / or EDMN to TETA and / or DETA is in the presence of THF performed.
  • THF the presence of THF during the subsequent hydrogenation, especially when the hydrogenation is carried out in suspension mode, can reduce the agglomeration tendency of the suspension catalysts used.
  • a particularly preferred embodiment of the present invention relates to a process for preparing TETA and / or DETA by hydrogenating EDDN and / or EDMN with hydrogen in the presence of a catalyst, characterized in that the preparation of EDDN and / or EDMN from FA, HCN and EDA is carried out in the presence of toluene as solvent and the hydrogenation is carried out in suspension mode in the presence of THF.
  • THF is supplied after the EDDN and / or EDMN preparation and that after the EDDN and / or EDMN preparation, a treatment of EDDN or EDMN with an adsorbent, preferably a solid, acidic adsorbent, in the presence of THF takes place.
  • an adsorbent preferably a solid, acidic adsorbent
  • the reaction of FA, HCN and EDA can be carried out according to the options a) to d) described there, the starting materials generally being converted to mixtures of EDDN and / or EDMN.
  • the preparation can be carried out, for example, by reacting a) HCN and EDA initially to FACH, which is subsequently reacted with EDA, or b) EDDN by reaction of an ethylenediamine-formaldehyde adduct (EDFA) or
  • EDMN prepared by reacting an ethylenediamine monoformaldehyde adduct (EDMFA) with hydrocyanic acid, wherein EDFA or EDMFA can be obtained by reacting EDA with FA, or that c) EDA is reacted with a mixture of formaldehyde and hydrogen cyanide, or that d ) EDA is reacted simultaneously with formaldehyde and HCN.
  • EDMFA ethylenediamine monoformaldehyde adduct
  • the options a) to d)) described in WO 2008/104579 are preferably carried out at a temperature of 10 to 90 ° C, in particular at 30 to 70 ° C.
  • the reaction can be carried out at atmospheric pressure or optionally also at elevated pressure (overpressure).
  • options a) to d) are carried out in a tubular reactor or a stirred tank cascade.
  • the reaction of FA, HCN and EDA can also be carried out as a continuous process, in particular as a large-scale process.
  • the process can be controlled so that the proportion of EDMN in the reaction product varies and EDMN is obtained not as a by-product, but as the second main reaction product.
  • the ratio of EDDN to EDMN in the reaction of FA, HCN and EDA is influenced by the molar ratio of the starting materials as described below.
  • EDDN and / or EDMN can be prepared according to option a) from HCN, FA and EDA, whereby first FA is reacted with HCN to FACH and subsequently FACH with EDA.
  • EDA can in principle be prepared by methods known to those skilled in the art
  • FACH Fluorescence-Activated Chemical Activated Access
  • Ullmann Article "Formaldehyde” in Ullmann's Encyclopedia of Industrial Chemistry, Günther Reuss, Walter Disteldorf, Armin Otto Gamer and Albrecht Hilt, Published Online: 15 JUN 2000, DOI: 10.1002 / 14356007.a1 1_619, It can be carried out, for example, by reacting formaldehyde with an aqueous blue acid.
  • Formaldehyde and hydrocyanic acid are also commercially available chemicals as described above.
  • formaldehyde as described above, used as a 30 to 50% aqueous solution.
  • Hydrocyanic acid can, as described above, be used in gaseous form or as an aqueous solution.
  • FACH A preferred variant for the production of FACH is described in WO 2008/104579.
  • the preparation of FACH can be carried out by reacting aqueous formaldehyde with hydrocyanic acid.
  • formaldehyde is present as a 30 to 50% aqueous solution
  • hydrocyanic acid is preferably used in 90 to 100% purity.
  • This reaction is preferably carried out at a pH of 5.5, which is preferably adjusted with sodium hydroxide or ammonia.
  • the reaction can be carried out at temperatures of 20 to 70 ° C, for example in the loop and / or tubular reactor.
  • purified hydrocyanic acid (HCN) and HCN crude gas can be chemisobiert in aqueous formaldehyde solution under the above conditions to FACH.
  • the crude HCN gas is preferably prepared by pyrolysis of formamide and, in addition to water, contains in particular small amounts of ammonia.
  • the resulting aqueous FACH solution can be concentrated by careful vacuum evaporation, for example with a falling-film or thin-film evaporator.
  • a concentration is carried out on a 50-80 wt .-% aqueous FACH solution.
  • stabilization of the FACH solution by lowering the pH to ⁇ 4, preferably to ⁇ 3, is advantageous, for example by addition of acid, for example by addition of phosphoric acid or preferably of sulfuric acid.
  • a 50 to 80% by weight aqueous solution of FACH is preferably used in the process according to option a).
  • EDDN / EDMN from EDA and FACH is preferably used in the process according to option a).
  • the molar ratio of EDA to FACH according to option a) in the reaction of EDA with FACH is in the range from 1: 1 to 1: 2 [mol / mol].
  • the molar ratio of EDA to FACH is preferably about 1: 1, 8 to 1: 2 [mol / mol], in particular about 1: 2 [mol / mol].
  • the molar ratio of EDA to FACH is preferably 1: 1.5 to 1: 2, more preferably 1: 1.8 to 1: 2.
  • a high EDDN content in the reaction mixture advantageous if EDDN is to be hydrogenated in a subsequent reaction to TETA.
  • the molar ratio of EDA to FACH is preferably 1: 1 to 1: 1.5, more preferably 1: 1 to 1: 1.3.
  • a higher EDMN content in the reaction mixture is advantageous when EDMN is to be hydrogenated in a subsequent reaction to DETA.
  • reaction of FACH and EDA can be carried out according to the general process conditions described above.
  • the reaction is carried out in the presence of one of the abovementioned organic solvents, in particular the preferred and particularly preferred organic solvents mentioned.
  • the amount of solvent used is generally 0.1 to 50 kg per kg, preferably 1 to 30 kg, more preferably 3 to 25 kg per kg of EDA used, as described above.
  • toluene As a particularly advantageous organic solvent, toluene has proven to be a technically simple and efficient method in a subsequent separation of water.
  • the educts and optionally the organic solvent (s) used, and optionally water, can be mixed before being introduced into the reactor or first in the reactor itself.
  • FACH is preferably mixed with an organic solvent, one of the foregoing organic solvents, especially toluene, to a FACH-containing stream, using either fresh organic solvent or organic solvent recovered from the subsequent work-up.
  • EDA as described above, is also preferably mixed with water to form an aqueous EDA stream before being introduced into the reactor when the subsequent reaction with FACH is carried out in an adiabatically operated reactor.
  • the educts and optionally solvents are fed separately or partially separated and the mixture is carried out in the reactor, for example by means of suitable internals.
  • an organic solvent is added to the reaction mixture prior to introduction into the reactor in order to limit the adiabatic increase in temperature when the reaction is carried out in an adiabatically operated reactor, ie in a reactor which is essentially not is cooled and in which the reaction temperature is increased by the liberated heat of reaction.
  • the organic solvents used can help limit the increase in temperature by absorbing heat of reaction according to their heat capacity and contributing to a lower temperature rise. In general, the higher the amount of supplied solvent, the more the temperature rise can be limited.
  • the organic solvent is cooled or added at ambient temperature to allow it to absorb heat.
  • the organic solvent is preferably introduced into the reactor at a temperature in the range from 10 to 50.degree. C., preferably from 15 to 45.degree. C. and more preferably from 20 to 40.degree
  • the use of organic solvents can - as described below - also accelerate cooling of the reaction mixture after it leaves the reactor, for example by depressurizing the solvent-containing reaction mixture so that at least part of the organic solvent evaporates. Due to the additional evaporation of the organic solvent, the reaction mixture can be additionally deprived of heat.
  • the reaction mixture is cooled at or after the outlet of the reactor, especially when the reaction is carried out in an adiabatically operated reactor.
  • the cooling of the reaction mixture can be carried out as described above and in more detail below.
  • the reaction of FACH and EDA takes place in a reactor with limited backmixing at a temperature in the range from 20 to 120 ° C., and a short residence time.
  • this particularly preferred embodiment relates to a
  • FACH formaldehyde cyanohydrin
  • EDA ethylenediamine
  • reaction of FACH and EDA is carried out in a reactor with limited backmixing.
  • Examples of a reactor with limited backmixing are a tube reactor and a stirred tank cascade.
  • the reaction of FACH and EDA is particularly preferably carried out in a tubular reactor ("plug flow reactor").
  • the ratio of height to diameter of the tubular reactor is preferably 1: 1 to 500: 1, more preferably 2: 1 to 100: 1, and most preferably 5: 1 to 50: 1.
  • the tubular reactor may contain internal internals that counteract backmixing.
  • the internals may be, for example, balls, screens, trays or static mixer.
  • an empty tube is used as tube reactor.
  • the location of the reactor is insignificant. It can be vertical or horizontal, or run as a spiral or sly.
  • the residence time in the reaction of FACH with EDA in the reactor in the claimed temperature range is 300 seconds or less, preferably 200 seconds or less, more preferably 100 seconds or less, and most preferably 60 seconds or less.
  • the residence time is in the range from 1 to 300 seconds, particularly preferably 5 to 200 seconds, very particularly preferably 10 to 100 seconds and particularly preferably 15 to 60 seconds.
  • the residence time is in the range from 1 to 300 seconds, particularly preferably 5 to 200 seconds, very particularly preferably 10 to 100 seconds and particularly preferably 15 to 60 seconds.
  • Dwell time ⁇ defined as quotient of reactor volume VR and outgoing volume flow
  • the reactor volume being the volume from the reactor inlet to the reactor
  • the reactor inlet corresponds to the mixing point at which FACH and EDA are brought into contact.
  • the reactor outlet corresponds to the point at which the temperature of the reaction mixture is lowered by cooling.
  • the reactor outlet corresponds to the point at which the reaction mixture enters the heat exchanger for cooling.
  • the reactor outlet corresponds to the last mixing point at the outlet of the reactor, at which further organic solvent is supplied for cooling.
  • the reactor outlet corresponds to the expansion valve, through which the reaction mixture is partially evaporated as described below.
  • the reactor volume also includes the parts of the pipe or supply lines to the reactor, which are brought into contact between the reactor inlet (mixing point, at the EDA and FACH) and the reactor outlet (eg expansion valve, inlet to the heat exchanger or the last one) Mixing point at the outlet of the reactor, to which organic solvent is supplied for cooling) are.
  • the FACH-containing stream and the aqueous EDA stream are mixed at the input of the reactor.
  • the mixing can take place by means of static mixers, suitable internals, such as packing, in particular Raschig rings, or by generating a turbulent flow on and after the mixing point.
  • a turbulent flow can be carried out by injection or injection of one of the starting materials in the other educt.
  • the reaction of EDA with FACH takes place in the temperature range from 20 to 120 ° C, preferably 25 to 100 ° C and particularly preferably in the range of 30 to 90 ° C.
  • the reaction of EDA with FACH in the most preferred embodiment is done under adiabatic conditions, i. the reaction temperature is increased by the released heat of reaction.
  • reaction temperature it is necessary for the reaction temperature not to exceed 120 ° C., since in the context of this invention an increased decomposition of the target products EDDN or EDMN was observed above this temperature.
  • the starting materials and optionally organic solvent and optionally water can be cooled to temperatures in the range of 10 to 50 ° C, preferably 20 to 40 ° C and particularly preferably 25 to 35 ° C before being introduced into the reactor;
  • the reactor or a part of the reactor can be provided with cooling devices;
  • One or more of the above measures may be combined.
  • the educts, and optionally organic solvent and water can be introduced at a temperature in the range of 10 to 50 ° C, preferably 15 to 40 ° C and particularly preferably 20 to 35 ° C in the reactor. If the temperature of the educts are above these preferred ranges, then the starting materials can be cooled down with suitable cooling devices, for example heat exchangers, in particular plate, tube bundle or double-jacket heat exchangers.
  • suitable cooling devices for example heat exchangers, in particular plate, tube bundle or double-jacket heat exchangers.
  • the reactor or part of the reactor may alternatively or additionally be provided with cooling devices.
  • the reactor may have a jacket cooling.
  • a part of the reactor contents is passed through a loop in which a heat exchanger is located.
  • additional cooling devices usually mean a higher expenditure on equipment and construction, but these are also suitable for keeping the temperature in the reactor in the range of the particularly preferred embodiment.
  • the reaction mixture may be cooled by adding further organic solvent before or during the reaction.
  • the total amount of organic solvent should preferably not be above 50 kg per kg of EDA, preferably 30 and more preferably 25 kg per kg of EDA.
  • the organic solvent for cooling at a temperature in the range of 10 to 50 ° C, preferably 15 to 40 ° C and particularly preferably 20 to 35 ° C is introduced into the reactor.
  • the outlet temperatures in the range of 50 to 120 ° C, preferably maintained in the range of 60 to 1 10 ° C and more preferably in the range of 70 to 100 ° C. become.
  • the cooling takes place both by adding organic solvent and by cooling the tubular reactor via a cooling jacket.
  • the reaction mixture is additionally cooled at the outlet of the reactor.
  • the cooling of the reaction mixture can be effected, for example, by cooling by means of suitable cooling devices, addition of further organic solvent or by flash evaporation. The cooling of the reaction mixture at the outlet of the reactor will be described in more detail below.
  • the preparation of EDDN and / or EDMN from EDFA or EDMFA can also be carried out according to option b) by reacting FA with EDA to form EDFA and / or EDMFA, which can then react further with HCN to give EDDN or EDMN.
  • EDA is first converted with FA to EDFA or EDMFA.
  • no organic solvent is added to EDFA or EDMFA before or during the reaction of EDA with FA.
  • the reaction preferably takes place in the presence of water, since FA, as described above, is preferably used in the form of aqueous solutions.
  • EDFA (II) is formally presented as a seminal for clarity.
  • the preparation of EDFA usually proceeds via the intermediate EDMFA (III), which is formed from one mole of EDA and one mole of formaldehyde.
  • the reaction of EDA with formaldehyde to EDFA is generally highly exothermic.
  • the enthalpy of reaction is between 100 and 120 kJ per mole of EDA.
  • EDA generally forms a hydrate with water in an exothermic reaction.
  • the amount of heat produced by hydrate formation, at about 25 kJ per mole of EDA, is usually about 20% of the total released heat.
  • the molar ratio of EDA to formaldehyde is 1 to 1.8 to 1 to 2.2, preferably 1 to 1.9 to 1 to 2.1, more preferably 1 to 2 to 1 to 2.1.
  • the molar ratio of EDA to FA is preferably 1: 1, 8 to 1: 2.2, more preferably 1: 1.9 to 1: 2.1.
  • a high EDFA content in the reaction mixture is advantageous when EDFA is reacted in a subsequent reaction with HCN to EDDN, which is to be further hydrogenated to TETA.
  • the molar ratio of EDA to FA is preferably 1: 0.8 to 1: 1, 5, more preferably 1: 1 to 1: 1, 3.
  • a higher EDMFA content in the reaction mixture is advantageous when EDMFA is reacted in a subsequent reaction with HCN to EDMN, which is to be further hydrogenated to DETA.
  • the pressure maintained during the reaction of EDA with FA is not critical and generally only needs to be high enough for the reactor contents to be liquid. It is not limited to the top and is preferably 1 to 10 bar, more preferably 2 to 5 bar.
  • the reaction of FA with EDA is preferably carried out continuously.
  • all reactors suitable for liquid phase reactions can be used.
  • the process according to option b) is preferably carried out in a tubular reactor or a stirred tank reactor or a loop reactor, in particular a loop reactor.
  • a loop reactor is to be understood below as a reactor in which the reactor contents are circulated.
  • the reaction entry can, after flowing through the reactor in a cooling device such as. B. cooled a heat exchanger, a partial stream of the cooled stream returned to the reactor and passed the residual stream in the next stage of the process become.
  • a cooling device such as. B. cooled a heat exchanger
  • It can be an internal or an external cycle.
  • the external circuit in a cooling device such as. B. a heat exchanger, in particular plate, tube bundle or double-jacket heat exchanger can be cooled.
  • the temperature rise in the reactor can be well controlled.
  • the residence time in the loop reactor is preferably 5 seconds to 60 minutes, more preferably 30 seconds to 20 minutes.
  • the conversion to EDFA or EDMFA takes place in a loop reactor in which backmixing occurs, the conversion is usually not complete. It is generally in the range of 50 to 99%. In a very particularly preferred embodiment, therefore, a combination of loop reactor and downstream tubular reactor is used as the reactor.
  • the conversion which can be in the range from 50 to 99% after leaving the loop reactor, as described above, can be further increased.
  • the downstream tubular reactor is preferably operated under the conditions of the loop reactor, preferably at the same pressure and temperature as the loop reactor
  • the starting materials can be mixed before being introduced into the reactor or only in the reactor itself.
  • static mixers As a mixing device, static mixers, turbulent flow piping, pumps or heat exchangers are generally suitable.
  • the mixture obtained by mixing EDA and FA is introduced into the loop of the loop reactor.
  • a mixing device is included in the reactor loop so that EDA and FA can be introduced into the reactor cycle via separate conduits and are recirculated in the mixer prior to introduction to the reactor section.
  • the temperature in the reaction of FA and EDA to EDFA or EDMFA is generally in the range of 0 to 100 ° C.
  • reaction of EDA and FA takes place in a narrow temperature range.
  • the particularly preferred embodiment relates to a Process for the reaction of ethylenediamine (EDA) with formaldehyde to ethylenediamine-formaldehyde adduct (EDFA) and / or ethylenediamine-monoformaldehyde adduct (EDMFA), characterized in that the reaction of FA with EDA at a temperature in the range of 20 to 50 ° C is performed.
  • EDA ethylenediamine
  • EDFA ethylenediamine-formaldehyde adduct
  • EDMFA ethylenediamine-monoformaldehyde adduct
  • the product of the reaction of FA and EDA prepared in the temperature range of 20 to 50 ° C has a small proportion of the minor components (IV) and (V), so that the yield of EDFA and / or EDMFA can be increased.
  • the temperature in the conversion of EDA with FA to EDFA and / or EDMFA is in the range from 20 to 50 ° C, preferably in the range from 25 to 45 ° C.
  • reaction is carried out in a loop reactor, more preferably in the previously described combination of loop reactor and tubular reactor.
  • EDFA or EDMFA is subsequently further reacted with HCN to give EDDN or EDMN after its preparation.
  • EDFA or EDMFA is preferably reacted with HCN without further work-up.
  • the molar ratio of EDFA to hydrocyanic acid (HCN) is preferably 1: 1, 8 to 1: 2.2, more preferably 1: 1, 9 to 1: 2.0.
  • the molar ratio of EDMFA to hydrocyanic acid is preferably 1: 1 to 1: 1, 3, more preferably 1: 1 to 1: 1.2.
  • reaction of EDFA and / or EDMFA and HCN can be carried out according to the general process conditions described above.
  • the reaction of EDFA or EDMFA with HCN is carried out in the presence of one of the abovementioned organic solvents, in particular the preferred and particularly preferred organic solvents mentioned.
  • the amount of solvent used is, as described above, generally from 0.5 to 50 kg per kg, preferably from 1 to 30 kg, more preferably from 3 to 25 kg per kg of EDA used.
  • Particular preference is also given to the reaction of EDFA or EDMFA with HCN in the presence of toluene.
  • the reaction pressure in the reaction of HCN with EDFA or EDMFA is generally not critical. Preference is given to setting a pressure at which the educts and any solvent used are present in the liquid phase.
  • the pressure is therefore preferably 1 bar to 10 bar, particularly preferably 1 to 5 bar and particularly preferably 1 to 3 bar.
  • the pressure preferably corresponds to the pressure which was set during the optionally previous conversion of FA with EDA to EDFA or EDMFA.
  • the organic solvent (s) used and optionally water can be mixed before being introduced into the reactor or only in the reactor itself.
  • the reaction is preferably carried out in a tubular reactor or a stirred tank cascade under adiabatic conditions, i. in a reactor which is essentially not cooled and the reaction temperature is raised by the heat of reaction liberated.
  • the reaction mixture generally exits at a temperature from the reactor which is above the inlet temperature.
  • the reaction mixture is cooled at the outlet of the reactor.
  • the cooling of the reaction mixture can be carried out as described above and in more detail below.
  • the reaction of EDFA or EDMFA with HCN takes place in a reactor with limited backmixing at a temperature in the range from 20 to 120 ° C. and a short residence time.
  • this particularly preferred embodiment relates to a
  • EDFA ethylenediamine-formaldehyde adduct
  • EDMFA ethylenediamine-monoformaldehyde adduct
  • HCN hydrocyanic acid
  • a reactor with limited backmixing are a tube reactor and a stirred tank cascade.
  • the reaction is particularly preferably carried out in a tubular reactor ("plug flow reactor").
  • the ratio of height to diameter of the tubular reactor is preferably 1: 1 to 500: 1, more preferably 2: 1 to 100: 1, and most preferably 5: 1 to 50: 1.
  • the tube reactor may contain internal internals which counteract backmixing in the longitudinal direction.
  • the internals may be, for example, balls, diaphragms, sieve plates or static mixers.
  • an empty tube is used as tube reactor.
  • the location of the reactor is insignificant. It can be vertical or horizontal, or run as a spiral or sly.
  • the residence time in the reactor in the claimed temperature range is 300 seconds or less, preferably 200 seconds or less, more preferably 100 seconds or less, and most preferably 60 seconds or less.
  • the residence time is in the range from 1 to 300 seconds, particularly preferably 5 to 200 seconds, very particularly preferably 10 to 100 seconds and particularly preferably 15 to 60 seconds.
  • the reactor inlet corresponds to the mixing-in point at which EDFA or EDMFA are brought into contact with HCN.
  • the reactor outlet corresponds to the point at which the temperature of the reaction mixture is lowered by cooling.
  • the reactor outlet corresponds to the point at which the reaction mixture enters the heat exchanger for cooling.
  • the reactor outlet corresponds to the last mixing point at the outlet of the reactor, at which further organic solvent is supplied for cooling.
  • the reactor outlet corresponds to the expansion valve, after which the reaction mixture is partially evaporated as described below.
  • the reactor volume also includes the parts of the pipe or feed lines to the reactor, which are connected between the reactor inlet (mixing point where EDFA and EDMFA are brought into contact with HCN) and the reactor outlet (eg expansion valve, inlet to the heat exchanger or last mixing point at the exit at which organic solvent is supplied for cooling).
  • the reactor inlet mixing point where EDFA and EDMFA are brought into contact with HCN
  • the reactor outlet eg expansion valve, inlet to the heat exchanger or last mixing point at the exit at which organic solvent is supplied for cooling.
  • the EDFA or FACH-containing stream and the HCN stream are mixed in the particularly preferred embodiment at the entrance of the reactor.
  • the mixing can be effected by means of static mixers, suitable internals, such as random packings, in particular Raschig rings, or by generating a turbulent flow at and after the mixing point.
  • the reaction of EDFA or EDMFA with HCN in this particularly preferred embodiment is in the temperature range from 20 to 120 ° C., preferably from 25 to 100 ° C. and particularly preferably in the range from 30 to 90 ° C.
  • the reaction of EDFA or EDMFA with HCN is carried out in the particularly preferred embodiment under adiabatic conditions, i. the reaction temperature in the reactor is increased by the liberated heat of reaction.
  • reaction temperature does not exceed 120 ° C., since in the context of this invention an increased decomposition of the target products EDDN or EDMN was observed above this temperature.
  • the starting materials and optionally organic solvent and optionally water can be cooled to temperatures in the range of 10 to 50 ° C, preferably 20 to 40 ° C and particularly preferably 25 to 35 ° C before being introduced into the reactor; the reactor or a part of the reactor can be provided with cooling devices; or
  • the educts, and optionally organic solvent and water can be introduced at a temperature in the range of 10 to 50 ° C, preferably 15 to 40 ° C and particularly preferably 20 to 35 ° C in the reactor. If the temperature of the educts are above these preferred ranges, then the starting materials can be cooled down with suitable cooling devices, for example heat exchangers, in particular plate, tube bundle or double-jacket heat exchangers.
  • suitable cooling devices for example heat exchangers, in particular plate, tube bundle or double-jacket heat exchangers.
  • the reactor or part of the reactor may alternatively or additionally be provided with cooling devices.
  • the reactor may have a jacket cooling.
  • a part of the reactor contents is passed through a loop in which a heat exchanger is located.
  • additional cooling devices usually mean a higher expenditure on equipment and construction, but these are also suitable for keeping the temperature in the reactor in the range of the particularly preferred embodiment.
  • the reaction mixture may be cooled by adding further organic solvent before or during the reaction.
  • the total amount of organic solvent should preferably not be above 50 kg per kg of EDA, preferably 30 and more preferably 25 kg per kg of EDA.
  • the organic solvent for cooling at a temperature in the range of 10 to 50 ° C, preferably 15 to 40 ° C and particularly preferably 20 to 35 ° C is introduced into the reactor.
  • the reaction mixture generally exits at a temperature from the reactor which is above the inlet temperature.
  • the outlet temperatures in the range of 50 to 120 ° C, preferably maintained in the range of 60 to 1 10 ° C and more preferably in the range of 70 to 100 ° C. become.
  • the cooling takes place both by adding organic solvent and by cooling the tubular reactor via a cooling jacket.
  • the reaction mixture is additionally cooled at the outlet of the reactor.
  • the cooling of the reaction mixture can be carried out, for example, by cooling by means of suitable cooling devices, addition of further organic solvent or by flash evaporation. The cooling of the reaction mixture at the outlet of the reactor will be described in more detail below.
  • the production of EDDN and / or EDMN can furthermore be carried out according to option c) by reacting EDA with a mixture of formaldehyde and hydrocyanic acid (GFB).
  • GFB formaldehyde and hydrocyanic acid
  • the reaction of EDA with a mixture of formaldehyde and hydrogen cyanide can be carried out according to the general process conditions described above.
  • the reaction is carried out in the presence of one of the abovementioned organic solvents, in particular the preferred and particularly preferred organic solvents mentioned.
  • the amount of solvent used is, as described above, generally from 0.5 to 50 kg per kg, preferably from 1 to 30 kg, more preferably from 3 to 25 kg per kg of EDA used.
  • reaction is preferably carried out in the presence of water, as also described above.
  • the molar ratio of FA and hydrocyanic acid in the GFB is generally in the range of 0.5: 1 to 1.5: 1.
  • the molar ratio of EDA to GFB is preferably 1: 1.5 to 1: 2 [mol / mol].
  • the molar ratio of EDA to GFB is 1: 1, 8 to 1: 2 [mol / mol].
  • the GFB is made by blending approximately equimolar amounts of formaldehyde and hydrogen cyanide.
  • the reaction mixture is cooled at the outlet of the reactor.
  • the cooling of the reaction mixture can be carried out as described above and in more detail below
  • EDA formaldehyde and hydrogen cyanide
  • the simultaneous (parallel) reaction of EDA with formaldehyde and hydrogen cyanide (HCN) can be carried out according to the general process conditions described above.
  • the molar ratio of EDA to formaldehyde to HCN is usually 1: 1, 5: 1, 5 to 1: 2: 2 [mol / mol / mol].
  • the molar ratio of EDA to formaldehyde to HCN is preferably 1: 1, 8: 1, 8 to 1: 2: 2 [mol / mol / mol].
  • the three reactant components added at the same time or stepwise in equal molar amounts, based on the total amount of educt in the reaction vessel.
  • the reaction is carried out in the presence of one of the abovementioned organic solvents, in particular the preferred and particularly preferred organic solvents mentioned.
  • the amount of solvent used is, as described above, generally from 0.5 to 50 kg per kg, preferably from 1 to 30 kg, more preferably from 3 to 25 kg per kg of EDA used.
  • the reaction mixture is cooled at the outlet of the reactor.
  • the cooling of the reaction mixture can be carried out as described above and in more detail below
  • the ratio of EDDN to EDMN can generally be influenced by the ratio of the educts used.
  • the weight ratio of EDDN to EDMN is generally from 30:70 to 95: 5, preferably from 50:50 to 95: 5, more preferably from 75:25 to 90:10
  • the reaction may optionally contain organic solvent.
  • the reaction product preferably contains one of the abovementioned or preferred and particularly preferred organic solvents.
  • the reaction effluent contains toluene.
  • the reaction discharge particularly preferably contains 5 to 30% by weight and very particularly preferably 10 to 20% by weight and more preferably 12 to 18% by weight of toluene, based on the reaction product.
  • the reaction discharge contains essentially no further organic solvents in addition to toluene.
  • the reaction effluent generally contains water which is formed in the reaction of FA, HCN and EDA as reaction water or which was fed together with the educts or separately.
  • the reaction product obtained in the production of EDDN or EDMN can be worked up further by methods known to those skilled in the art. This relates for example to the separation of the reaction product from unreacted starting material and any solvent present.
  • the reaction mixture from the reaction of EDA, HCN and FA after leaving the reactor and cooled before working up Accordingly, the particularly preferred embodiment relates to a
  • Cooling of the reaction mixture from the reaction of FA, EDA and HCN is particularly preferred when the last stage of the reaction was carried out in an adiabatically operated reactor, in particular a tubular reactor.
  • the temperature after cooling in the range of 20 to 70 ° C, more preferably in the range of 20 to 60 ° C and particularly preferably in the range of 30 to 50 ° C.
  • the cooling of the reaction mixture can be carried out by means of suitable cooling devices, such as heat exchangers, in particular plate, tube bundle or double-shell heat exchangers.
  • the total amount of organic solvent should preferably not be above 50 kg per kg of EDA, preferably 30 and more preferably 25 kg per kg of EDA.
  • the organic solvent is used for cooling at a temperature in the range of 10 to 50 ° C, preferably 15 to 40 ° C and more preferably 20 to 35 ° C introduced into the reactor.
  • the cooling is most preferably carried out by flash evaporation.
  • the reaction mixture from the EDDN or EDMN preparation is usually expanded into a container under reduced pressure via a valve at the outlet of the last reactor in which EDDN or EDMN production takes place.
  • the reduced pressure is preferably adjusted so that some of the water used and the components which boil more easily than EDDN or EDMN are converted into the gas phase in the reaction effluent and the educts, such as EDMN or EDDN, as well as part of the water, and If necessary, organic solvent remain in the liquid phase.
  • flash evaporation a portion of the water is removed from the reaction mixture in a gentle manner.
  • the withdrawn heat of vaporization the liquid EDDN or EDMN-containing phase is cooled.
  • 10 to 80 wt .-%, particularly preferably 20 to 70 wt .-% and most preferably 30 to 60 wt .-% of the water present in the reaction mixture is evaporated in the flash evaporation and transferred to the gas phase.
  • the reduced pressure is 1000 mbar and less, more preferably 300 mbar and less and most preferably 200 mbar and less.
  • the reduced pressure is 10 to 1000 mbar, preferably 50 to 300 mbar and particularly preferably 100 to 200 mbar.
  • the proportion of the components present in gaseous form after the flash evaporation is preferably partially condensed in a cooler, the condensation preferably being operated in such a way that water and any solvent used are substantially completely condensed.
  • Lighter boiling components e.g. Ammonia, HCN, methanol or CO2 are preferably not condensed and can be removed in gaseous form or supplied to combustion.
  • the work-up of the condensed phase may depend on whether the reaction of EDA with HCN and FA was carried out in the presence of an organic solvent and then which organic solvent was used.
  • the aqueous condensate can be fed to the column K2 described below, in which low boilers are separated from water. It is also possible to supply the water for disposal, for example, a wastewater treatment.
  • the condensed mixture of organic solvent and water is usually separated by distillation into an aqueous stream and a solvent-containing stream, the solvent-containing Stream is preferably recycled to the process or can be introduced into a column K1 described below.
  • the aqueous stream can generally be introduced into a water treatment. If, in a preferred embodiment, a solvent which has a miscibility gap with water or which is essentially insoluble in water is used as the organic solvent, the condensed mixture is preferably fed to a phase separator, so that the condensed phase is in a phase which forms the phase contains organic solvents, and an aqueous phase can be separated.
  • the separation of organic solvent and water can generally be carried out without additional distillation. Furthermore the separated water after the phase separation can then generally be introduced directly into a sewage treatment plant or recycled into the process, for example for mixing EDA with water.
  • organic solvents in which the amount of solvent dissolved in the aqueous phase is very low are particularly preferred.
  • examples include toluene, cyclohexane, Metyhlcyclohexan, octane, heptane and xylenes.
  • the aqueous phase obtained after the phase separation can also be introduced into a distillation apparatus K2, in which water is separated off as the bottom product from lower-boiling organic components.
  • the water thus separated off can be recycled, for example, as a solvent into the process (for example for the production of an aqueous EDA solution) or fed to a sewage treatment plant or to a biological wastewater treatment.
  • the organic low boilers separated off by distillation during the distillation in the column K2 for example organic solvents which are lighter than water or solvents which form a low-boiling azeotrope with water, HCN or toluene
  • the organic low-boiling components can be fed to the condenser connected downstream of the flash evaporation.
  • the organic phase obtained after the phase separation is preferably passed into the column K1 described below or recycled as organic solvent in the process.
  • the EDDN- or EDMN-containing reaction product which is in the liquid phase after flash evaporation into the reduced pressure vessel is preferably fed, as described below, to a distillation column K1 in which water is depleted of EDDN and EDMN, respectively.
  • an organic solvent was used in the EDDN or EDMN production, which under the conditions of EDDN or EDMN production has a miscibility gap with water or in water a low solubility, so form in the container in which Discharge from the EDDN or EDMN production was relaxed, usually two liquid phases, namely an aqueous EDDN or EDMN phase and a phase containing the organic solvent.
  • the two phases separately or together fed to a column K1. It is further preferred that when the column contains K1 packing, both liquid phases separated from each other to lead to separate liquid distributor.
  • EDMN accumulates, be further worked up by methods known in the art. This relates for example to the separation of the reaction product from unreacted starting material and any solvent present. Working up of the reaction product from EDDN or EDMN production
  • reaction product obtained in the production of EDDN or EDMN can be worked up further by methods known to those skilled in the art. This relates for example to the separation of the reaction product from unreacted starting material and any solvent present.
  • the reaction discharge from the EDDN or EDMN preparation is preferably worked up by firstly i) carrying out a low boiler separation and then ii) carrying out a water depletion.
  • the depletion of the low boilers is preferably carried out by stripping.
  • the reaction effluent from the EDDN or EDMN production can be stripped with nitrogen in order to remove traces of hydrocyanic acid, which can occur, for example, as a decomposition product of FACH.
  • the separation of low-boiling components can also be effected by distillation.
  • the residence time in the distillation be kept short, for example by carrying out the distillation in a falling film evaporator or wiped film evaporator.
  • the low boiler removal as described above, by flash evaporation.
  • the flash evaporation has the advantage that the low boiler removal and the cooling of the reaction can be carried out in one process step.
  • the water depletion after the depletion of low boilers preferably takes place in a distillation column K1.
  • the column is generally operated so that an aqueous stream is withdrawn at the top of the column, while at the bottom of the column an EDDN or EDMN-containing stream is withdrawn.
  • the discharge from the EDDN or EDMN preparation is preferably fed together with the distillation agent (as defined below) into the upper region, preferably at the top, of a distillation column K1.
  • the aqueous EDDN or EDMN aqueous phase and the organic solvent are separately supplied to the column K1 as a distillation agent. It is further preferred that if the column contains K1 packing, both liquid phases on a separate liquid keitsverteiler to lead.
  • the organic solvent as distillation agent into the stripping section of the column, preferably into the lower section of the column, and more preferably into the bottom of the column.
  • HCN which may be contained in the recycled organic solvent, can react with EDMN to EDDN. This can reduce the amount of HCN removed.
  • the distillation column K1 preferably has internals for increasing the separation efficiency.
  • the distillative internals may, for example, be in the form of an ordered packing, for example as a sheet-metal package such as Mellapak 250 Y or Montz Pak, type B1 -250. There may also be a pack of lesser or increased specific surface area, or a tissue pack or pack of other geometry such as Mellapak 252Y may be used.
  • the advantage of using these distillative internals is the low pressure loss and the low specific liquid hold-up in comparison to, for example, valve trays.
  • the installations can be in one or more beds.
  • the number of theoretical plates is generally in the range of 3 to 25, preferably 5 to 15.
  • the top pressure in the column K1 is preferably adjusted so that the bottom temperature is in the range specified below.
  • the bottom temperature is 100 ° C or less because it has been found in the present invention that EDMN or EDDN is unstable in the presence of water at higher temperatures and decomposes to undesirable by-products.
  • a bottom temperature in the range of less than 100 ° C, more preferably less than 80 ° C and most preferably less than 60 ° C is set. More preferably, the bottom temperature is in the range of 20 to 100 ° C, more preferably in the range of 30 to 80 ° C and most preferably in the range of 40 to 60 ° C.
  • the copying pressure is preferably 10 mbar to 1 bar, more preferably 30 mbar to 700 mbar and most preferably 50 to 500 mbar.
  • the top pressure in the column K1 is less than 300 mbar, more preferably 100 to 200 mbar and most preferably 130 to 180 mbar.
  • the formation of deposits in the column internals, in particular the column packings can be substantially reduced in the temperatures which are established in the column at these head pressures.
  • the distillation is carried out in the presence of an organic solvent which has a boiling point between water and EDDN and / or EDMN at the distillation pressure prevailing in the column or which forms a low-boiling azeotrope with water.
  • This particularly preferred embodiment thus relates to a A process for the preparation of EDDN and / or EDMN by reacting FA, HCN and EDA, wherein the reaction is carried out in the presence of water, and depleted after the reaction water from the reaction mixture in a distillation column, characterized in that the distillation in the presence of a organic solvent is carried out, which has a boiling point between water and EDDN and / or EDMN at the prevailing distillation column in the column or which forms a low-boiling azeotrope with water.
  • the organic solvent which has a boiling point between water and EDDN and / or EDMN at the distillation pressure prevailing in the column or which forms a low-boiling azeotrope with water is referred to below as the distillation medium.
  • Preferred distillers are the organic solvents mentioned at the beginning which have a boiling point between water and EDDN and / or EDMN or which form a low-boiling azeotrope with water.
  • the distillation agent is already supplied before or during the reaction of FA, HCN and EDA.
  • the amount of organic solvent is generally 0.1 to 50 kg per kg, preferably 1 to 30 kg, more preferably 3 to 25 kg per kg of EDA used.
  • the amount of distillation agent should generally be such that in the column bottom of the distillation column K1 - as described above, preferably a bottom temperature in the range of less than 100 ° C, more preferably less than 80 ° C and most preferably less than 60 ° C is set.
  • the bottom temperature is in the range of 20 to 100 ° C, more preferably in the range of 30 to 80 ° C and most preferably in the range of 40 to 60 ° C.
  • the bottom temperature is 100 ° C or less because it has been found in the present invention that EDMN or EDDN is unstable in the presence of water at higher temperatures and decomposes to undesirable by-products.
  • distillation agent If the distiller forms a low boiling azeotrope with water, then it is necessary that the amount of distillation agent be sufficient to be on the correct "side" of the azeotrope, ie that the amount of distillation agent must be sufficient to contain the head
  • the amount of solvent required can be routinely determined by a person skilled in the art, depending on the chosen distillation agent, from generally known tables and reference books for azeotropes.
  • the top pressure in the column K1 is, as described above, preferably 10 mbar to 1 bar, more preferably 30 mbar to 700 mbar and most preferably 50 to 500 mbar. In a very particular embodiment, the top pressure in the column K1 is less than 200 mbar, more preferably 100 to 200 mbar and most preferably 130 to 180 mbar. In the context of this invention it has been recognized that in the case of those head pressures in the column adjusting temperatures, the formation of deposits in the column internals, in particular the column packs, can be substantially reduced.
  • the condenser of the distillation column K1 is generally operated at a temperature at which most of the water or water azeotrope is condensed at the corresponding top pressure.
  • the operating temperature of the capacitor is in the range of 20 to 70 ° C, preferably 25 to 50 ° C.
  • the condenser generally accumulates a condensate which contains essentially water or a light-weighting water azeotrope.
  • the condensate of the column K1 can either be discharged or returned to the process. Possibly. the condensate can be separated before recirculation or discharge in water and distillation, for example by distillation. For example, the distillation of water in the previously described column K2 can be carried out.
  • distillation medium has a miscibility gap with water
  • separation of water and distillation agent can also be effected by means of phase separation.
  • the vapors from the top of the column K1 are fed to the condenser, at which the vapors which are formed in the flash vaporization, ie. that the vapors from the column K1 and from the flash evaporation are driven onto a common condenser.
  • the EDDN or. EDMN-containing mixture preferably contains the distillate used in the distillative removal of water.
  • the EDDN or. EDMN-containing mixture from the bottom of the column K1 preferably 5 to 30 wt .-% toluene and most preferably 10 to 20 wt .-% and particularly preferably 12 to 18 wt .-%, based on the discharged sump.
  • EDMN-containing mixture from the bottom of column K1 contains-in contrast to the amounts of more than 10% by weight described in the prior art-preferably less than 3% by weight, more preferably less than 1 wt .-% water, most preferably less than 0.5 wt .-% and particularly preferably less than 0.3 wt .-% water.
  • the resulting EDDN- or EDMN-containing mixture can be directly hydrogenated in a subsequent reaction with hydrogen and in the presence of a catalyst to DETA or TETA. Treatment with adsorbent
  • the EDDN- or EDMN-containing mixture after the water depletion is purified before the hydrogenation of the EDDN or EDMN to form TETA or DETA, in which the EDDN- or EDMN-containing mixture is treated with an adsorbent treated.
  • the treatment is carried out with a solid, acidic adsorbent.
  • a solid, acidic adsorbent it has been found that with solid, acidic adsorbents, the service life of hydrogenation catalysts in the subsequent hydrogenation can be extended to DETA or TETA. Furthermore, it has been found that the formation of the by-products aminoethylpiperazine (AEPIP) which occur in the hydrogenation of EDDN or EDMN, which as a rule are associated with the loss of activity of the catalyst, can be reduced.
  • AEPIP aminoethylpiperazine
  • step a) Methods for reacting FA, HCN and EDN in the presence of water (step a)) have been described above.
  • low-boiling components such as HCN or methanol
  • HCN or methanol low-boiling components
  • the reaction effluent from the EDDN or EDMN preparation for example by stripping or flash evaporation
  • the water-containing EDDN or EDMN subsequently fed to a distillation in which water is depleted
  • the distillation is carried out as described above in the presence of a distillation agent (definition see above).
  • the EDDN or EDMN mixture from stage b) preferably contains 95% by weight EDDN and / or EDMN and more, particularly preferably 97% by weight and more, very particularly preferably 99% by weight and more, based on the EDDN mixture minus the distilling agent contained in the EDDN mixture and / or solvent-free ("distillate-free and solvent-free" calculated).
  • the mixture obtained from stage b) preferably contains the distillate used in the depletion of water.
  • the EDDN or EDMN mixture from step b) preferably contains 5 to 30 wt .-% toluene, particularly preferably 10 to 20 wt .-% toluene, and most preferably 12 to 18 wt. -%.
  • the EDDN or EDMN mixture from stage b) contains preferably 5 to 50 Gew. -% EDDN and / or EDMN, particularly prefers 8 to 30 Gew. -% EDDN and / or EDMN, and most preferably 10 to 20 wt .-% EDDN and / or EDMN.
  • the EDDN or EDMN mixture obtained from stage b) preferably contains less than
  • step c) the EDDN or EDMN obtained from stage b) is treated with a solid, acidic adsorbent in the presence of an organic solvent.
  • Suitable solvents are all organic solvents which can be used for the reaction of EDDN or EDMN. As mentioned above, it is preferred that the organic solvents used are stable under the conditions of EDDN and EDMN hydrogenation, respectively.
  • the organic solvent is fed before the treatment of the EDDN or EDMN mixture from step b) with the adsorbent.
  • the concentration of EDDN and / or EDMN in the mixture which is treated with the adsorbent in the range of 5 to 50 wt .-%, particularly preferably 8 to 30 wt .-% and very particularly preferably 10 to 20 wt .-% is.
  • the water content of organic solvents supplied after EDDN and / or EDMN preparation and before or during the treatment of the EDDN and / or EDMN with adsorbent have a low water content, since it was found that low Amounts of water in the treatment with adsorbent can reduce the absorbency of the adsorbent and in the subsequent hydrogenation of EDDN or EDMN polar impurities can be introduced, leading to undesirable side reactions.
  • the organic solvent fed in more preferably contains less than 0.5% by weight of water, more preferably less than 0.3% by weight of water, very preferably less than 0.1% by weight of water and particularly preferably less than 0 , 03 wt .-% water.
  • THF is supplied as organic solvent. When THF was used, particularly good catalyst service lives could be achieved in the subsequent hydrogenation. If the subsequent hydrogenation is carried out in suspension mode, the use of THF can reduce the agglomeration tendency of suspension catalysts during the hydrogenation.
  • solid, acidic adsorbent is understood as meaning a water-insoluble porous material which, owing to its large surface area, can bind water or other molecules to it by physical or chemical forces
  • An acidic adsorbent usually has functional groups that behave under the conditions of adsorption as Bronsted or Lewis acids.
  • an acidic sorbent is able to retain preferred basic substances compared to less basic substances.
  • Preferred solid acidic adsorbents are acidic metal oxides such as silica, titania, alumina, boria (B2O3), zirconia, silicates, aluminosilicates, borosilicates, zeolites (especially in H form), acid ion exchangers, and silica gel, e.g. Sorbead WS from BASF SE, or mixtures of these substances.
  • acidic metal oxides such as silica, titania, alumina, boria (B2O3), zirconia, silicates, aluminosilicates, borosilicates, zeolites (especially in H form), acid ion exchangers, and silica gel, e.g. Sorbead WS from BASF SE, or mixtures of these substances.
  • Very particularly preferred solid, acidic adsorbents are silicon dioxide and silica gel.
  • silica gels e.g. can be prepared by acidification of aqueous sodium silicate solutions and drying of the silica sols initially obtained, as described for example in Hollemann-Wiberg (Textbook of Inorganic Chemistry, 102nd edition, Verlag Walter Gruyter, 2007, page 962).
  • Examples of particularly preferred silica gels are Sorbead WA from BASF SE and Silikagel KG 60 from Merck KGaA.
  • the solid, acidic adsorbent is a substance selected from the group consisting of silica, titania, alumina, boria (B2O3), zirconia, silicates, aluminosilicates, borosilicates, zeolites (especially in the H form), acidic ion exchangers and silica gel.
  • the feature solid acidic adsorbent comprises neither activated carbon nor non-acidic (basic) ion exchangers.
  • the treatment of the obtained in step b) EDDN or EDMN mixture with organic solvent can be carried out either continuously, semi-continuously or discontinuously.
  • the treatment can be carried out batchwise, for example by bringing the adsorbent into contact with the EDDN or EDMN in the presence of an organic solvent.
  • the treatment can be carried out by suspending the adsorbent in the mixture to be purified, for example by stirring in a suitable container.
  • the treatment time in the batchwise treatment is generally in the range of 1 minute to 48 hours, preferably 5 minutes to 24 hours, more preferably 1 hour to 16 hours and particularly preferably 2 to 8 hours.
  • the amount of adsorbent is preferably in the range from 0.1 to 25% by weight, more preferably in the range from 0.5 to 20% by weight and very particularly preferably in the range from 1 to 10% by weight, based on the sum of EDDN, EDMN and organic solvent.
  • the pressure is usually not critical. However, it is preferred to set a pressure at which the mixture to be purified is liquid.
  • the pressure is usually 1 to 10 bar.
  • the treatment is generally carried out at temperatures of less than 150 ° C, preferably less than 100 ° C, more preferably less than 80 ° C and most preferably less than 60 ° C.
  • the discontinuous treatment with adsorbent can be carried out under an inert gas atmosphere, for example under nitrogen or argon.
  • the adsorbent can be separated by suitable methods of EDDN or EDMN, for example by filtration, centrifugation or sedimentation.
  • the treatment of the mixture to be purified takes place continuously.
  • the mixture to be purified is passed over one or more fixed beds or beds of the adsorbent.
  • the adsorbent may also be arranged in the form of a fluidized bed
  • the fixed bed or the bed is preferably arranged in a tube or a heat exchanger.
  • the fixed bed or the bed is generally traversed by the mixture to be purified.
  • the load is preferably 0.01 to 20, more preferably 0.05 to 15 and most preferably 0.1 to 10 kg to be purified mixture per kg of adsorbent per hour.
  • the fixed bed volume and the size of the adsorbent particles can be varied within wide limits and thus adapted to the selected reaction conditions and the process conditions.
  • the particle size of the solid, acid adsorbents used is preferably 0.1 to 10, particularly preferably 0.5 to 6 and very particularly preferably 1 to 4 mm, since it has been found that particles which are too large have negative diffusion effects and too small particles can lead to blockages in the adsorber ,
  • the particles are spherical.
  • the adsorbent is present in a fixed bed in carousel arrangement, in particular with regeneration, i. Two or more fixed beds are alternatively flowed through, so that the unused fixed beds can be regenerated.
  • the pressure is usually not critical. However, it is preferred to set a pressure at which the mixture to be purified is liquid.
  • the pressure is usually 1 to 10 bar.
  • the treatment is carried out, as described above, usually at temperatures of less than 150 ° C, preferably less than 100 ° C, more preferably less than 80 ° C and most preferably less than 60 ° C.
  • the continuous treatment with adsorbent can be carried out under an inert gas atmosphere, for example under nitrogen or argon.
  • the adsorbent or parts of the adsorbent e.g. Abrieb
  • suitable methods of EDDN or EDMN for example by filtration, centrifugation or sedimentation.
  • the regeneration of the adsorbent can be carried out by washing with water, preferably by washing with dilute aqueous acids, more preferably first by washing with water and then by washing with dilute aqueous acids.
  • dilute, organic acids are preferably used, more preferably
  • the concentration of acids in the dilute aqueous acids is 10% by weight or less.
  • the sorbent is dried by introducing a dry gas such as air or nitrogen.
  • a dry gas such as air or nitrogen.
  • the sorbent and / or the gas is warmed up.
  • the sorbent is dried by passing a dry organic solvent over it.
  • a dry organic solvent is the same organic solvent that is used in the subsequent hydrogenation or that is already present in the treatment with adsorbent.
  • the dry organic solvent preferably contains 1% by weight of water or less, particularly preferably 0.5% by weight or less, very particularly preferably 0.1% by weight or less and especially preferably 0.05% by weight or fewer.
  • the dry organic solvent can be passed either liquid or vapor over the adsorbent.
  • the mixture from stage c) preferably comprises EDDN and / or EDMN together with the organic solvent in the presence of which the treatment with adsorbents has been carried out and, if appropriate, distillation agent which was preferably present during the water depletion. Possibly. the mixture from stage c) may contain further organic solvents.
  • the water content of the mixture from stage c) is preferably lower than the water content of the EDDN or EDMN mixture before the treatment with adsorbent, since the adsorbent also has a drying effect.
  • the water content of the mixture from stage c) is preferably 0.1% by weight or less, more preferably 0.03% by weight or less.
  • the EDDN or EDMN mixture obtained from stage c) can be purified; for example, the optionally added organic solvent can be separated off from EDDN or EDMN.
  • the mixture obtained from c) is preferably fed directly to the hydrogenation without further work-up.
  • Nitriles of the formula (I) can be converted into amines of the formula (II)
  • R is -NH-CH 2 -CH 2 -NH 2 I in which R 1 is hydrogen or radicals of the formula
  • J x x integers from zero to two mean hydrogenation.
  • the hydrogenation of nitriles of the formula (I) preferably takes place according to the conditions described below.
  • the amount of Raney cobalt or Raney nickel is generally from 1 to 60 wt .-%, preferably 5 to 40 wt .-%, particularly preferably 20 to 30 wt .-%, based on the total reaction mixture.
  • the catalytic hydrogenation of the nitriles of the formula (I) to give corresponding amines is carried out at temperatures of 60 to 150.degree. C., preferably 80 to 140.degree. C., particularly preferably 100 to 130.degree.
  • the total pressure in the reactor is generally 60 to 325 bar, preferably 100 to 280 bar, more preferably 170-240 bar.
  • at least two moles of hydrogen are required per nitrile group.
  • the hydrogenation can be carried out continuously or batchwise, but preferably continuously in the presence of an organic solvent.
  • the organic solvent must be inert under the hydrogenation conditions. By inert is meant that the solvent does not participate in the chemical reactions. In addition, it should have the highest possible solubility for hydrogen.
  • Ether as tetrahydrofuran, 2-methyltetrahydrofuran, 3-methyltetrahydrofuran, dioxane, methyl tert-butyl ether, diisobutyl ether, glycol dimethyl ether, diglycol dimethyl ether, aliphatic and aromatic hydrocarbons such as toluene, N-methylpyrrolidone or mixtures proved to be the preferred organic solvents for the hydrogenation of these connections.
  • the nitrile of the formula (I) is dissolved after low boiler and water separation and before adsorptive purification.
  • the amine which is formed in the hydrogenation of the corresponding nitrile can be used as a solvent.
  • the settling rate of the hydrogenation catalyst in the chosen organic solvent should be low in order to keep the catalyst well in suspension.
  • the catalyst is suspended in the reaction mixture to be hydrogenated.
  • the amount of organic solvent is 1 to 99, preferably 5 to 95, particularly preferably 50 to 90 wt .-%, based on the sum of organic solvent and nitrile of the formula (I).
  • Suitable reactors are all hydrogenation reactors known to those skilled in the art, in which the cobalt or nickel catalyst can be suspended. Examples include stirred tanks, Strahlsch secured-, Strahldüsen- and bubble column reactors.
  • Raney cobalt or Raney nickel, solvent and / or amine are usually introduced into the stirred reactor under hydrogen pressure and temperature. Subsequently, nitrile of the formula (I) dissolved in one of the solvents mentioned is usually metered in.
  • nitrile of the formula (I) dissolved in one of the solvents mentioned is usually metered in.
  • the rate of hydrogen addition generally depends on the rate of nitrile conversion and the ability to dissipate the heat of reaction of the highly exothermic nitrile hydrogenation.
  • Raney cobalt or Raney nickel and solvent When starting a continuous hydrogenation Raney cobalt or Raney nickel and solvent is usually initially charged in a stirred reactor. After pressing in hydrogen and heating, nitrile of the formula (I) dissolved in the solvent is generally added to the respective solvent and an appropriate amount is discharged from the reactor. The total pressure is generally kept constant during the reaction time by repressing hydrogen. Unreacted hydrogen can be recycled to the hydrogenation reactor after cooling and depressurization of the reaction and recompression as cycle gas in the rule. But it is also possible not to return the hydrogen and instead use it elsewhere or dispose of it.
  • the residence time in the reactor is in a continuous procedure generally 0.1 to 6 hours, preferably 0.5 to 2 hours.
  • the catalyst loading is usually 0.1 to 10 kg, preferably 0.5 to 5 kg of nitrile of the formula (I) per kg of Raney cobalt catalyst and hour.
  • the catalyst loading, based on the catalyst surface is preferably 0.25-10 -5 to 5-10 "5 kg EDDN + EDMN per m 2 of catalyst surface area and per hour, and most preferably 5 to 0,5-10- 2- 10- 5 kg EDDN + EDMN per m 2 the power input via the stirrer is preferably 0.1 to 100 KW per m 3.
  • Used catalyst can generally be separated by filtration, centrifugation or cross-flow filtration. It may be necessary to compensate losses of original amount of catalyst by attrition and / or deactivation by adding fresh catalyst.
  • the workup of the hydrogenation is preferably carried out by distillation.
  • the regeneration of the catalyst is carried out as described above.
  • an adsorbent preferably a solid, acid adsorbent
  • an organic solvent preferably THF.
  • the treatment is analogous, as described in the EDDN and / or EDMN production. Hydrogenation of EDDN and / or EDMN
  • Raney catalysts the above-described and preferred Raney catalysts are preferably used.
  • the hydrogenation of EDDN or EDMN to TETA or DETA is generally carried out by reacting EDDN or EDMN with hydrogen in the presence of a catalyst and an organic solvent.
  • EDDN or EDMN preferably takes place-as described above-in accordance with one of the options a) to d) described above, in particular of the preferred embodiments described therein.
  • reaction mixture from the EDDN or EDMN production is cooled, preferably by flash evaporation.
  • reaction mixture from the EDDN or EDMN preparation is purified, preferably, as described, by depletion of low boilers, preferably by flash evaporation, and subsequent distillation to deplete water, preferably in the presence of a distillation agent.
  • the EDDN or EDMN mixture after depletion of water is treated with an adsorbent, preferably as described with a solid, acidic adorbent.
  • the mixture which is introduced into the hydrogenation preferably contains EDDN and / or EDMN.
  • the proportion of EDDN and / or EDMN in the mixture that is fed to the hydrogenation is preferably in the range from 5 to 50% by weight, particularly preferably 8 to 30% by weight and very particularly preferably 10 to 20% by weight. % is.
  • the mixture introduced into the hydrogenation contains the organic solvent present in the treatment with adsorbent.
  • TETA or DETA takes place in the presence of hydrogen.
  • the hydrogen is generally used technically pure.
  • the hydrogen can also be used in the form of a hydrogen-containing gas, that is to say with admixtures of other inert gases, such as nitrogen, helium, neon, argon or carbon dioxide.
  • inert gases such as nitrogen, helium, neon, argon or carbon dioxide.
  • reformer effluents, refinery gases, etc. may be used if and when these gases contain no contact poisons for the hydrogenation catalysts used, such as CO.
  • preference is given to using pure hydrogen or essentially pure hydrogen in the process for example hydrogen having a content of more than 99% by weight of hydrogen, preferably more than 99.9% by weight of hydrogen, particularly preferably more than 99.99 Wt .-% hydrogen, in particular more than 99.999 wt .-% hydrogen.
  • TETA or DETA preferably takes place in the presence of an organic solvent.
  • the organic solvent is the same solvent that was present in the treatment with adsorbent. However, it is also possible to add another solvent or to separate the solvent which was present during the treatment with adsorbent and to add a new solvent.
  • organic solvent it is possible to use all organic solvents which can be used in the preparation of EDDN or EDMN, in particular the organic solvents mentioned as preferred.
  • the weight ratio of organic solvent to EDDN or EDMN during the hydrogenation is preferably 0.01: 1 to 99: 1, more preferably 0.05: 1 to 19: 1 and most preferably 0.5: 1 to 9: 1.
  • the hydrogenation is carried out in the presence of THF, since in THF the agglomeration tendency of catalysts in the suspension mode of operation can be reduced.
  • the hydrogenation particularly preferably takes place in the presence of THF so much that the content of EDDN and / or EDMN during the hydrogenation is preferably in the range from 5 to 50% by weight, more preferably 8 to 30% by weight and most preferably 10 to 20 wt .-% is.
  • the hydrogenation of EDDN or EDMN can also be carried out in the presence of water.
  • EDDN or EDMN which contains less than 3% by weight, preferably less than 1% by weight, particularly preferably less than 0.5% by weight of water and particularly preferably less than 0.3% by weight. , based on EDDN or EDMN contains.
  • EDDN and / or EDMN having a low water content is obtained by treating the EDDN and / or EDMN with adsorbent.
  • the hydrogenation takes place in the presence of basic compounds, which are preferably in suitable solvents, such as alkanols, such as C 1 -C 4 -alkanols, e.g. Methanol or ethanol, or ethers, such as cyclic ethers, e.g. THF or dioxane are added to the reaction mixture.
  • suitable solvents such as alkanols, such as C 1 -C 4 -alkanols, e.g. Methanol or ethanol
  • ethers such as cyclic ethers, e.g. THF or dioxane are added to the reaction mixture.
  • solutions of alkali metal or alkaline earth metal hydroxides or of hydroxides of the rare earth metals in water, particularly preferably solutions of LiOH, NaOH, KOH and / or CsOH.
  • the concentration of alkali metal and / or alkaline earth metal hydroxide, based on the mixture to be hydrogenated is in the range from 0.005 to 1% by weight, particularly preferably from 0.01 to 0, 5 wt .-% and most preferably 0.03 to 0.1 wt .-% is.
  • amides and / or amines such as ammonia and EDA.
  • the amount of by-products formed such as AEPIP, can be reduced in the hydrogenation.
  • Preferred examples of such additives are ammonia and ethylenediamine.
  • the amount of these additives is 0.01 to 10 moles per mole of EDDN + EDMN.
  • the basic additives can generally be fed batchwise or continuously and before and / or during the hydrogenation.
  • TETA or DETA is generally carried out by reacting EDDN or EDMN with hydrogen in the presence of a hydrogenation catalyst and an organic solvent.
  • the temperatures are generally in a range of 60 to 150 ° C, preferably from 80 to 140 ° C, especially at 100 to 130 ° C.
  • the pressure prevailing in the hydrogenation is generally from 5 to 400 bar, preferably from 60 to 325 bar, particularly preferably from 100 to 280 bar and particularly preferably from 170 to 240 bar.
  • the pressure in the hydrogenation using Raney catalysts in the range of 170 to 240 bar since in this pressure range, the formation of AEPIP can be reduced.
  • the formation of AEPIP can accelerate the deactivation of the catalyst. Accordingly, the particularly preferred embodiment relates to a
  • EDDN or the aminonitrile mixture containing EDDN is fed at a rate of hydrogenation which is not greater than the rate at which EDDN and optionally the other components of the aminonitrile mixture react with hydrogen in the hydrogenation.
  • Hydrogenation of EDDN to TETA generally requires at least four moles of hydrogen per mole of EDDN.
  • Hydrogenation of EDMN to DETA generally requires at least two moles of hydrogen per mole of EDMN.
  • reaction of EDDN or EDMN with hydrogen in the presence of catalysts can be carried out continuously, semicontinuously or discontinuously in conventional reaction vessels suitable for catalysis in a fixed bed, fluidized bed, suspension mode. Reaction vessels are suitable for carrying out the hydrogenation, in which it is possible to contact the EDDN or EDMN and the catalyst with the hydrogen under pressure.
  • the hydrogenation in suspension mode can be carried out in a stirred reactor, jet loop reactor, jet nozzle reactor, bubble column reactor, or in a cascade of such identical or different reactors.
  • the hydrogenation on a fixed bed catalyst preferably takes place in one or more tube reactors but also tube bundle reactors.
  • the hydrogenation of the nitrile groups takes place with the release of heat, which usually has to be removed.
  • the heat dissipation can be achieved by built-in heat exchanger surfaces,
  • Cooling jackets or external heat transfer in a circulating circuit around the reactor can be run in straight passage.
  • a circulation procedure is possible in which a part of the reactor discharge is returned to the reactor inlet, preferably without prior workup of the circulation stream.
  • the circulation stream can be cooled by means of an external heat exchanger in a simple and cost-effective manner and thus the heat of reaction can be dissipated.
  • the reactor can also be operated adiabatically. With adiabatic operation of the reactor, the temperature rise in the reaction mixture can be limited by cooling the feeds or by supplying "cold" organic solvent.
  • a simple and cost-effective design is possible.
  • An alternative is a cooled tube bundle reactor (only in the case of the fixed bed).
  • a combination of the two modes is conceivable.
  • a fixed bed is followed by a suspension reactor.
  • the catalyst can be arranged in a fixed bed (fixed-bed mode) or suspended in the reaction mixture (suspension mode).
  • the catalyst is suspended in the reaction mixture to be hydrogenated.
  • the settling rate of the hydrogenation catalyst in the chosen solvent should be low in order to keep the catalyst in good suspension.
  • the particle size of the catalysts used in the suspension procedure is therefore preferably between 0.1 and 500 ⁇ m, in particular 1 and 100 ⁇ m. If the hydrogenation of EDDN or EDMN in suspension mode is carried out continuously, EDDN or EDMN are preferably fed continuously into the reactor and a stream which contains the hydrogenation products TETA or DETA is continuously removed from the reactor. In the discontinuous suspension procedure, EDDN or EDMN are initially charged together with organic solvent.
  • the amount of catalyst in the batchwise batchwise process is preferably from 1 to 60% by weight, more preferably from 5 to 40% by weight, and most preferably from 20 to 30% by weight, based on the total reaction mixture.
  • the residence time in the reactor is preferably 0.1 to 6 hours, more preferably 0.5 to 2 hours, in the case of a discontinuous suspension procedure.
  • the residence time in the reactor is preferably 0.1 to 6 hours, more preferably 0.5 to 2 hours, in a continuous suspension procedure.
  • the catalyst loading in the continuous suspension procedure is preferably 0.1 to 10 kg, preferably 0.5 to 5 kg EDDN + EDMN per kg catalyst and hour.
  • the catalyst loading based on the catalyst surface preferably 10 "6 to 10" 4 kg EDDN + EDMN per m 2 of catalyst surface area and per hour, wherein the catalyst surface according to the BET method (DIN 66131).
  • the catalyst loading based on the catalyst surface 0.25 10 "5 to 5-10” 5 kg EDDN + EDMN per m 2 of catalyst surface area and per hour and is most preferably 0.5-10 "5 to 2-10 "5 kg EDDN + EDMN per m 2 catalyst surface area and hour.
  • the particularly preferred embodiment relates to a
  • a process for the preparation of TETA and / or DETA by reacting EDDN and / or EDMN with hydrogen in the presence of a catalyst in suspension characterized in that the catalyst loading, based on the catalyst surface 10 -6 to 10 -4 kg EDDN + EDMN per m 2 of catalyst surface and hour, the catalyst surface being determined according to the BET method.
  • the power input via the stirrer is preferably 0.1 to 100 KW per m 3 .
  • Used catalyst can be separated by filtration, centrifugation or cross-flow filtration. It may be necessary to compensate for losses of original amount of catalyst by attrition and / or deactivation by adding fresh catalyst.
  • the catalyst is disposed in a fixed catalyst bed.
  • the catalyst loading in the continuous hydrogenation in the fixed bed reactor is preferably 0.1 to 10 kg, preferably 0.5 to 5 kg EDDN + EDMN per kg of catalyst and hour.
  • the catalyst loading, based on the catalyst surface preferably 10 "6 to 10" 4 kg EDDN + EDMN per m 2 of catalyst surface area and per hour, wherein the catalyst surface according to the BET method (DIN 66131).
  • the catalyst loading based on the catalyst surface 0.25 10 "5 to 5-10” 5 kg EDDN + EDMN per m 2 of catalyst surface area and per hour and is most preferably 0.5-10 "5 to 2-10 "5 kg EDDN + EDMN per m 2 of catalyst surface and hour. Accordingly, the particularly preferred embodiment relates to a
  • a process for the preparation of TETA and / or DETA by reacting EDDN and / or EDMN with hydrogen in the presence of a catalyst in a fixed bed characterized in that the catalyst loading, based on the catalyst surface 10 -6 to 1 CH kg EDDN + EDMN per m 2 catalyst surface and hour, wherein the catalyst surface is determined according to the BET method.
  • the reaction effluent from the hydrogenation usually also contains other higher or lower-boiling organic substances as by-products, such as methylamine, AEPIP, PIP or TEPA or basic compounds or additives which were added before or during the hydrogenation, for example alkali metal hydroxides, alcoholates, Amides, amines and ammonia.
  • the hydrogenation product preferably further contains organic solvent which was present during the hydrogenation, preferably the organic solvent which was also present during the treatment with adsorbent, in particular THF.
  • the reaction effluent further preferably contains distillation agents, in particular toluene, which was preferably used in the distillative depletion of water after EDDN or EDMN production.
  • the reaction generally also contains small amounts of water.
  • the amounts of water contained in the effluent from the hydrogenation correspond to the quantities which originate from the EDDN or EDMN preparation and the workup preferably carried out.
  • the effluent from the hydrogenation may optionally be further purified.
  • the catalyst can be separated by methods known to those skilled in the art.
  • the hydrogen present during the hydrogenation is separated off.
  • the separation of hydrogen is preferably carried out by lowering the pressure at which the hydrogenation was carried out to a value at which hydrogen is gaseous, the other ren components in the reaction but in the liquid phase.
  • the reaction product is from a hydrogenation pressure of
  • THF low-boiling components
  • Hydrogen and optionally ammonia can be recycled to the hydrogenation of EDDN or EDMN.
  • THF can be condensed out and recovered.
  • THF may be recovered by scrubbing with a higher boiling solvent such as toluene or TETA.
  • Organic solvents present in the reaction discharge are generally likewise removed by distillation.
  • the main products can be isolated from the reaction product together or individually by methods known to those skilled in the art. If the two main products are isolated together, for example by distillation, they can then be separated into the two individual products. Ultimately, you will get pure TETA and pure DETA. Other impurities, byproducts or other ethylene amines such as TEPA or PIP can also be separated from the respective product by methods known to those skilled in the art.
  • TETA may also be isolated together with diaminoethylpiperazine or piperazinyl ethyl ethylenediamine formed in minor amounts.
  • the workup of the hydrogenation from the hydrogenation of EDDN is preferably carried out by distillation.
  • the hydrogenation effluent contains THF
  • EDMN polar impurities can be introduced, which lead to undesirable side reactions.
  • THF and water form a low-boiling azeotrope.
  • the separation of THF is carried out by a process for separating a reaction effluent which is reacted with hydrogen in the reaction of EDDN or EDMN Presence of THF and a catalyst is obtained, which TETA or DETA, water and optionally higher and lower than TETA or DETA boiling organic compounds, characterized in that
  • hydrogen is first separated from the reaction effluent.
  • the separation of hydrogen preferably by lowering the pressure at which the hydrogenation was carried out to a pressure at which hydrogen is gaseous, the other components in the reaction but in the liquid phase.
  • the reaction effluent from a hydrogenation pressure of preferably 60 to 325 bar, more preferably 100 to 280 bar, and most preferably 170 to 240 bar to a pressure of 5 to 50 bar relaxed in a container.
  • a hydrogenation pressure preferably 60 to 325 bar, more preferably 100 to 280 bar, and most preferably 170 to 240 bar to a pressure of 5 to 50 bar relaxed in a container.
  • At the top of the container are hydrogen and possibly ammonia, and a small amount of vaporized low-boiling such as THF obtained.
  • Hydrogen and optionally ammonia can be recycled to the hydrogenation of EDDN or EDMN.
  • THF can be condensed out and recovered. Alternatively, THF can be recovered by scrubbing with a higher boiling solvent such as toluene or TETA
  • the fraction of the reaction output which has remained liquid after the expansion is preferably passed into a column DK1.
  • the exact operating conditions of the distillation column can be routinely determined by the skilled person on the basis of the known vapor pressures and evaporation equilibria of the components introduced into the distillation column according to the separation performance of the distillation column according to conventional calculation methods.
  • the column is preferably designed as a tray column.
  • a tray column In a tray column are located in the interior of the column shelves on which the mass transfer takes place. Examples of different soil types are sieve trays, tunnel trays, dual-flow trays, bubble trays or valve trays.
  • the column preferably has a stripping section and a reinforcing section. But it can also have only one output part.
  • the number of theoretical plates is generally in the range of 5 to 30, preferably 10 to 20.
  • the pressure of the column is preferably chosen so that a bottom temperature in the range of 100 to 250 ° C is established.
  • the top pressure is 1 to 30 bar, more preferably 3 to 25 bar.
  • the operating temperature of the capacitor is in the range of 30 to 70 ° C, preferably 35 to 50 ° C.
  • low-boiling components such as ammonia or methylamine
  • This stream can subsequently be supplied to combustion.
  • condenser condensate precipitates mainly the separated azeotrope of water and THF.
  • the condensate or a part of the condensate is fed to an organic solvent which is substantially immiscible with water and which has a higher boiling point under the distillation conditions in the column DK1 than the forming THF / water azeotrope, which is deducted at the top of the column.
  • organic solvents which are essentially immiscible with water are those organic solvents in which less than 500 ppm by weight of water can be dissolved.
  • Preferred organic solvents which are substantially immiscible with water are toluene, n-heptane, n-octane, n-nonane and the like.
  • the amount of organic solvent fed which is substantially immiscible with water, is generally chosen to cause phase failure and to separate the phases by conventional engineering means such as separation in a phase separation vessel.
  • the weight ratio of organic solvent fed, which is substantially immiscible with water, to condensate is preferably 0.1: 1 to 10: 1, more preferably 0.5: 1 to 5: 1, and most preferably 0.8: 1 to 2 : 1.
  • the resulting mixture of condensate and organic solvent, which is substantially immiscible with water, is preferably passed into a phase separator where it decomposes into an aqueous phase and a phase containing THF and the substantially water immiscible solvent.
  • a phase separator where it decomposes into an aqueous phase and a phase containing THF and the substantially water immiscible solvent.
  • the phase containing THF and the substantially water-immiscible solvent, in the upper region of the column DK1 preferably recycled to the top of the column DK1.
  • the bottoms discharge contains less than 1 wt .-%, more preferably less than 1000 ppm by weight and more preferably less than 200 ppm by weight of water.
  • the bottoms discharge from column DK1 also contains TETA or DETA, THF, the substantially water-immiscible solvent, and optionally further organic solvent (which derives from dehydration and phase separation) and generally organic by-products, such as PIP, AEPIP and TEPA ,
  • the bottom product from column DK1 is passed into a distillation column DK2, in which THF is removed overhead and at the bottom of the column a stream is withdrawn, the TETA or DETA and the substantially water-immiscible solvent and, if necessary Contains additional toluene.
  • the exact operating conditions of the distillation column can be routinely determined according to the separation efficiency of the column used by the skilled person on the basis of the known vapor pressures and evaporation equilibria of the introduced into the distillation column components according to conventional calculation methods.
  • the column is preferably designed as a tray column.
  • a tray column In a tray column are located in the interior of the column shelves on which the mass transfer takes place. Examples of different soil types are sieve trays, tunnel trays, dual-flow trays, bubble trays or valve trays.
  • the column preferably has only one stripping section.
  • the number of theoretical plates is generally in the range of 5 to 30, preferably 10 to 20.
  • the top pressure is more preferably 200 mbar to 5 bar, particularly preferably 500 mbar to 2 bar.
  • a temperature is preferably set which is above the evaporation temperature of THF, so that THF is essentially completely converted into the gas phase.
  • a temperature is set at the bottom of the column, which is in the range of 100 to 250 ° C.
  • the condenser of the distillation column DK2 is generally operated at a temperature at which the major part of the THF is condensed at the corresponding top pressure.
  • the operating temperature of the capacitor is in the range of 30 to 70 ° C, preferably 35 to 50 ° C.
  • a condensate accumulates, which essentially contains THF.
  • This THF preferably contains less than 200 ppm by weight, more preferably less than 100 ppm by weight, of water, so that it is particularly suitable for recycling to the working up of the reaction effluent or the EDDN or EDMN preparation.
  • a bond can be created between the EDDN or EDMN hydrogenation and the EDDN or EDMN production, which reduces the amounts of organic solvents required.
  • the condensate at the top of the column DK2 may also contain traces of the organic solvent, which is substantially immiscible with water. Nevertheless, as described above, the condensate can be recycled to the EDDN or EDMN workup, since these solvents, as described above, are also a preferred organic solvent in this step.
  • the amount of organic solvent which is substantially immiscible with water, reduced in the condensate by a precondensator is connected upstream of the top of the column, which is operated in the temperature range of 80 to 150 ° C, preferably 100 to 130 ° C.
  • the number of trays in the enrichment section of the column DK2 can be increased and / or a portion of the condensate can be added as reflux to the column.
  • the molecular sieve has a pore diameter of less than 4 A, so that only water and ammonia are retained, but not other amines such as methylamine and ethylamine. The absorption capacity of the molecular sieve as adsorbent for the separation of water is thereby increased.
  • the bottom product from column DK2 is passed into a column DK3, in which a stream is withdrawn at the top, which contains predominantly toluene and / or the substantially water-immiscible solvent, and as the bottom product, a stream is withdrawn, the predominantly TETA or DETA, AEPIP and generally contains the by-products PIP, AEPIP and TEPA.
  • the exact operating conditions of the distillation column can be routinely determined according to the separation efficiency of the column used by the skilled person on the basis of the known vapor pressures and evaporation equilibria of the introduced into the distillation column components according to conventional calculation methods.
  • the distillation column preferably has internals for increasing the separation efficiency.
  • the distillative internals may, for example, be in the form of an ordered packing, for example as a sheet-metal package such as Mellapak 250 Y or Montz Pak, type B1 -250. There may also be a package of lesser or increased specific surface area, or a fabric packing or other geometry package such as Mellapak 252Y may be used.
  • the advantage of using these distillative internals is the low pressure loss and the low specific liquid hold-up in comparison to, for example, valve trays.
  • the installations can be in one or more beds.
  • the column preferably has a stripping and a reinforcing part.
  • the bottoms discharge from column DK2 is preferably supplied in a spatial range between 30% and 90% of the theoretical plates of the distillation column (counted from below), more preferably in a spatial range between 50% and 80% of the theoretical plates of the distillation column.
  • the feed may be slightly above the center of the theoretical plates. The optimum feed point can be determined by the skilled person with the usual calculation tools.
  • the number of theoretical plates is generally in the range of 3 to 25, preferably 5 to 15.
  • a temperature is set at the bottom of the column, which is in the range of 100 to 250 ° C.
  • the top pressure is preferably 10 mbar to 1 bar, particularly preferably 30 mbar to 500 mbar.
  • the condenser of the distillation column is usually operated at a temperature at which most of the toluene and / or the substantially water-immiscible solvent is condensed at the appropriate top pressure.
  • the operating temperature of the capacitor is in the range of 30 to 70 ° C, preferably 35 to 50 ° C.
  • a condensate which essentially contains toluene and / or the substantially water-immiscible organic solvent is obtained.
  • the toluene thus obtained and / or the substantially water-immiscible organic solvent can be recycled to the process, for example by feeding it to the condensate from column DK1.
  • toluene and / or the essentially water-immiscible organic solvent can also be fed to the EDDN or EDMN work-up, for example before the flash evaporation. In this way it is possible to achieve an economic connection.
  • DK3 At the bottom of the column DK3 usually falls to a stream containing TETA or DETA, and generally the by-products AEPIP, PIP and TEPA.
  • This bottoms discharge can be worked up further by conventional methods and separated into the individual constituents.
  • the bottoms discharge from column DK3 is passed into a column DK4, in which a mixture of PIP, AEPIP and DETA is obtained at the top, a mixture of pentamines, such as TEPA and other high boilers is obtained at the bottom and a side draw TETA stream is withdrawn with a purity of more than 99 wt .-%.
  • the exact operating conditions of the distillation column can be routinely determined according to the separation efficiency of the column used by the skilled person on the basis of the known vapor pressures and evaporation equilibria of the introduced into the distillation column components according to conventional calculation methods.
  • the distillation column preferably has internals for increasing the separation efficiency.
  • the distillative internals may, for example, be in the form of an ordered packing, for example as a sheet-metal package such as Mellapak 250 Y or Montz Pak, type B1 -250. There may also be a package of lesser or increased specific surface area, or a fabric packing or other geometry package such as Mellapak 252Y may be used.
  • the advantage of using these distillative internals is the low pressure loss and the low specific liquid hold-up in comparison to, for example, valve trays.
  • the installations can be in one or more beds.
  • the column preferably has a stripping and a reinforcing part.
  • the bottoms discharge from column DK3 is preferably supplied in a spatial range between 30% and 90% of the theoretical plates of the distillation column (counted from below), more preferably in a spatial range between 50% and 80% of the theoretical plates of the distillation column.
  • the feed may be slightly above the center of the theoretical plates. The optimum feed point can be determined by the skilled person with the usual calculation tools.
  • the number of theoretical plates is generally in the range of 5 to 30, preferably 10 to 20.
  • the top pressure is more preferably 1 mbar to 400 mbar, more preferably 5 mbar to 300 mbar.
  • a temperature is preferably set which is above the evaporation temperature of toluene, so that toluene passes substantially completely into the gas phase.
  • a temperature is set at the bottom of the column, which is in the range of 150 to 250 ° C.
  • the condenser of the distillation column is usually operated at a temperature of preferably 30 to 70 ° C, more preferably 35 to 50 ° C.
  • the condensate is condensed, which essentially contains a mixture of DETA, PIP and AEPIP.
  • Part of the condensate can be recycled as reflux into the column DK4.
  • At the bottom of the column DK4 usually falls to a stream which contains substantially en mixture of pentaamines, such as TEPA, and other high boilers.
  • TEPA pentaamines
  • the side stream is preferably withdrawn below the feed line of the bottom stream from column DK4, preferably in the range of 10% to 60%, more preferably in the range of 15 to 35% of the theoretical plates of the distillation column (counted from below).
  • the side draw preferably contains more than 99% by weight, more preferably more than 99.5% by weight TETA.
  • the regeneration of the catalysts is carried out as described above.
  • the TETA or DETA produced by the process according to the invention, as well as the preferred embodiments generally has a high quality and is thus particularly suitable for further reactions, for example for reaction with epoxy compounds for the production of epoxy resins or for reaction with acids for the production of Amides or polyamides.
  • Another object of the present invention is therefore also a process for the preparation of epoxy resins or amides or polyamides, characterized in that in a first stage TETA and / or DETA is prepared according to the invention, and in a second stage, the TETA or DETA thus obtained Epoxy resins, amides or polyamides is implemented.
  • FIG. 1 shows the production of EDDN or EDMN from EDA (1) and FACH (5).
  • EDA (1) is mixed with water (2) in a mixer (I) to form an aqueous EDA stream (3).
  • the mixture of EDA with water releases heat of hydration, which is dissipated in a heat exchanger (II).
  • An FACH-containing stream (5) is mixed with toluene (6).
  • the toluene-containing FACH stream is mixed at a mixing point with the aqueous EDA solution (3) and introduced into an adiabatically operated tubular reactor (III).
  • the exiting reaction mixture (7) is expanded at a pressure relief valve.
  • the forming gaseous phase (8) which contains water, toluene and low-boiling compounds, is condensed on a condenser (V). Uncondensed components (9), such as ammonia, HCN, methanol or CO2, are removed from the process.
  • the condensate (10) condensed on the condenser (V) is introduced into a phase separation vessel (VI) and separated into an aqueous phase (14) and a toluene-containing phase (11).
  • the aqueous phase (14) from the phase separation vessel (VI) can be recycled to the process, for example, for the preparation of an aqueous EDA solution in mixer (I) or in a biological wastewater treatment can be initiated (not shown).
  • the aqueous phase (14) can also be introduced into a column K2 (VIII), in which water is used as the bottom product (16). separated from low-boiling components (15).
  • the low boilers (15), for example lighter than water-boiling solvents or low-boiling water azeotropes or HCN, can be passed directly to the condenser (V), on which the gaseous phase from the flash evaporation is also condensed. Non-condensable components are discharged as stream (9) from the process.
  • the toluene-containing phase (11) can be recycled as an organic solvent in the process and mixed with the FACH-containing stream from the FACH production.
  • losses of toluene can be supplemented by a toluene supplement.
  • the toluene-containing phase (11) can preferably be introduced together with the liquid phase (12) from the flash template (IV) into a column K1 (VII).
  • a gaseous, substantially aqueous overhead product is withdrawn, which is passed directly to the condenser (V) and passed into the phase separation vessel (VI).
  • the phase separation vessel as described above, forming aqueous phase (15) is discharged, passed into the mixer (I), or the column K2 (VIII) are supplied.
  • a mixture of EDDN or EDMN and toluene is withdrawn.
  • the mixture (17) of toluene and EDDN or EDMN is diluted with THF (18) and treated in an adsorber (IX) with adsorbent, preferably with a solid, acidic adsorbent. From the adsorber, a mixture of EDDN and / or EDMN with toluene and THF (20) is obtained, which contains only small amounts of water.
  • the EDDN or EDMN mixture can be passed into a hydrogenation in which EDDN or EDMN is hydrogenated to TETA or DETA.
  • FIG. 2 shows the preparation of EDDN or EDMN from FA (1), EDA (2) and HCN (5), wherein first FA (1) and EDA (2) are converted to EDFA and / or EDMFA (4) , which then reacts with HCN (5) to EDDN or EDMN.
  • FA (1) is mixed with EDA (2) in the loop of a loop reactor (I).
  • FA (1) is reacted with EDA (2) to EDFA and / or EDMFA.
  • Part of the reactor contents of the loop reactor is discharged (3) and passed into a tubular reactor (II).
  • the discharge (4) from the tubular reactor (II) is mixed at the inlet of a tubular reactor (III) at a mixing point with HCN (5) and toluene (6) and passed through the pipe reactor (III).
  • the exiting reaction mixture (7) is expanded at a pressure relief valve.
  • the forming gaseous phase (8) which contains predominantly water and toluene, is condensed on a condenser (V). Uncondensed components (9), such as ammonia, HCN, methanol or CO2, are removed from the process.
  • the condensate (10) condensed on the condenser (V) is introduced into a phase separation vessel (VI) and separated into an aqueous phase (14) and a toluene-containing phase (11).
  • the aqueous phase (14) from the phase separation vessel (VI) can be recycled to the process, for example, for the preparation of an aqueous EDA solution in mixer (I) or in a biological wastewater treatment can be initiated (not shown).
  • the aqueous phase (14) can also be introduced into a column K2 (VIII), in which water as the bottom product (16) is separated off from low-boiling components (15).
  • the low boilers (15) for example lighter than water-boiling solvents or low-boiling water azeotropes or HCN, can be passed directly to the condenser (V). Non-condensable components are discharged as stream (9) from the process.
  • the toluene-containing phase (11) can be recycled to the process as an organic solvent and mixed with the EDFA-containing stream from the EDFA preparation.
  • losses of toluene can be supplemented by a toluene supplement.
  • the toluene-containing phase (11) can also be introduced into a column K1 (VII) together with the liquid phase (12) from the flash template (IV).
  • a gaseous, substantially aqueous overhead product is passed directly to the condenser (V) and passed into the phase separation vessel (VI), where the aqueous phase (15), as described above, discharged into the mixer (I) passed, or the column K2 (VIII) can be supplied.
  • a mixture of EDDN or EDMN and toluene is obtained.
  • the mixture of toluene and EDDN or EDMN (17) is diluted with THF (18) and treated in an adsorber (IX) with adsorbent, preferably with a solid, acidic adsorbent.
  • adsorbent preferably with a solid, acidic adsorbent.
  • a mixture of EDDN and / or EDMN with toluene and THF is obtained, which contains only small amounts of water.
  • the EDDN or EDMN mixture can be passed into a hydrogenation in which EDDN or EDMN is hydrogenated to TETA or DETA.
  • FIG. 3 shows the production of TETA or DETA from EDDN or EDMN.
  • EDDN or EDMN which can be prepared by reacting FA, HCN and EDA according to one of the options mentioned in the description a) to d), and which has been worked up, preferably by i) removal of low boilers, for example by stripping, flash evaporation or Distillation and ii) distilling off water, preferably in the presence of an organic solvent which has a boiling point between water and EDDN or EDMN under the conditions of water separation or which forms an azeotrope which boils gently with water, is referred to as "unpurified” in FIG.
  • Such "unpurified” EDDN or EDMN is mixed with THF (18) and treated in an adsorber with adsorbent, preferably solid, acidic adsorbent.
  • FIG. 4 shows the production of TETA or DETA from EDDN or EDMN with subsequent workup.
  • EDDN or EDMN can be prepared by reacting FA, HCN and EDA according to one of the options a) to d) mentioned in the description.
  • the workup is carried out, preferably by i) removal of low boilers, for example by stripping, flash evaporation or distillation and ii) depletion of water, preferably in the presence of an organic solvent which under the conditions of water separation has a boiling point between water and EDDN or EDMN or which forms a slightly boiling azeotrope with water.
  • the dewatered EDDN is preferably mixed with THF and treated with adsorbent, preferably solid, acidic adsorbent.
  • adsorbent preferably solid, acidic adsorbent.
  • the mixture (1) of EDDN or EDMN and THF is hydrogenated in a hydrogenation reactor (I) in the presence of supplied hydrogen (2) to TETA or DETA.
  • the reaction product from the hydrogenation (3) is expanded into a flash tank (II).
  • the gaseous constituents (4) such as hydrogen, parts of the THF, HCN, methanol or methylamine, can be discharged from the process or recovered partially or completely.
  • the liquid remaining after the expansion phase (5) is passed into a column K1, which has a stripping and a rectifying section.
  • a low-boiling THF / water azeotrope (6) is withdrawn and condensed.
  • the condensed stream is mixed with toluene (7) in a phase separation vessel.
  • an aqueous phase (8) and a THF / toluene phase (9) is formed, which is recycled to the column K1.
  • a stream (10) is withdrawn containing TETA, DETA, THF, toluene and organic compounds such as PIP, AEPIP and TEPA.
  • This stream (10) is passed into a column K2, in which THF is taken off as top product (1 1).
  • This THF (11) can be recycled directly to the process, preferably in the treatment of EDDN or EDMN with adsorbent.
  • the THF (11) Prior to introduction into the adsorber stage, the THF (11) may be contacted with a molecular sieve to further deplete water.
  • a stream (12) is withdrawn containing TETA, DETA, toluene and organic compounds such as PIP, AEPIP and TEPA.
  • This stream (12) is introduced into a column K3 in which toluene is drawn off at the top (13).
  • the withdrawn toluene (13) can be passed to dehydration of THF via line (7) in a phase separation vessel in which it is combined with the condensate (6) from column K1.
  • the withdrawn toluene (13) can also be discharged from the process via line (14) or preferably be used as a solvent in EDDN and / or EDMN production.
  • the bottom product of the column K3 (16) contains TETA, DETA, toluene and organic compounds such as PIP, AEPIP and TEPA.
  • This mixture can be further separated in the column K4 become.
  • low boilers such as PIP, AEPIP and DETA can be withdrawn overhead (17) and TETA taken off as side draw (18).
  • High boilers, such as TEPA, can be withdrawn at the sump (19).
  • the overhead or bottom stream can be separated into its individual constituents in subsequent distillation stages.
  • EDA ethylenediamine
  • Ethylenediamine-formaldehyde bisadduct EDFA
  • ECMFA Ethylenediamine-Formaldehyde Monoadduct
  • Ethylenediamine monoacetonitrile EDMN
  • TETA Triethylenetetramine
  • TEPA Tetraethylenepentamine
  • Iminodiacetonitrile (IDAN) The process according to the invention is explained in more detail with reference to the examples listed below.
  • Example 1 a) Deactivated Raney cobalt (composition: Ra-Co 2724, Grace) from the continuous hydrogenation of crude EDDN (89.3% EDDN, 4.5% EDMN, 5.4% BCMI, 0.8 % EDTriN) at 120 ° C and 210 bar (15 wt.% EDDN in a mixture of THF (80 wt.%) And toluene (20 wt.%)) And a catalyst loading of 1 g EDDN / g catalyst and Hour was extended after a period of 1 14 hours. The TETA yield fell from 86.3% to 60.3% during this period. In contrast, the AEPIP yield increased from 3.1% to 7.6%.
  • the catalyst was dried in vacuo ( ⁇ 10 mbar) at 80 ° C and passivated with air.
  • the elemental analysis showed a carbon content of 1, 4 wt .-% and a nitrogen content of 1, 0 wt .-%.
  • the deactivated catalyst (5 g) was stirred in an autoclave with 90 g of THF and 20 g of liquid ammonia (water content ⁇ 0.5% by volume) for 12 hours at 160 ° C. and a hydrogen pressure of 30 bar.
  • Example 1 a shows that deposits containing carbon and nitrogen can be removed from the deactivated Raney cobalt catalyst by treatment with liquid ammonia (Table 1).
  • Crude EDDN (15 wt .-% EDDN, dissolved in a mixture of 80 wt .-% THF and 20 wt .-% toluene) was passed continuously at 25 ° C via an adsorber, which with 30 g of silica gel 60 (Fa. Merck, 60 angstroms, 0.2-0.5 mm grain size).
  • the purified EDDN solution was continuously hydrogenated with hydrogen at 120 ° C. and 210 bar in the presence of 5 g of suspended Raney cobalt (composition of Ra-Co, Ra-Co 2724, Grace) for 1000 hours.
  • the catalyst loading was 1 g EDDN per g Raney cobalt and hour.
  • the TETA yield dropped from 88.3% to 78.9%.
  • the yield of by-product AEPIP increased from 2.1% to 7.8%.
  • Example 2 Analogously to Example 1 a deactivated Raney cobalt from the EDDN hydrogenation in vacuo ( ⁇ 10 mbar) was dried at 80 ° C and passivated with air. The elemental analysis revealed a carbon content of 2.8% by weight and a nitrogen content of 1.0% by weight.
  • the deactivated catalyst (500 mg) was stirred in an autoclave with 7 ml of a 10% by weight aqueous NaOH solution for 10 hours at 100 ° C. and a hydrogen pressure of 25 bar.
  • Example 2a shows that carbon deposits can not be removed from the deactivated Raney cobalt catalyst by treatment with aqueous sodium hydroxide solution (Table 2). In addition, cobalt leaching was observed.
  • the catalyst was dried in vacuo ( ⁇ 10 mbar) at 80 ° C and passivated with air.
  • the elemental analysis showed a carbon content of 2.5 wt .-% and a nitrogen content of 1, 4 wt .-%.
  • the deactivated catalyst 500 mg was stirred in an autoclave with 7 mL of a 25 wt .-% aqueous ammonia solution for 10 hours at 130 ° C and a hydrogen pressure of 25 bar. After evaporating the ammonia and drying again, the elemental analysis of the regenerated Raney cobalt gave a carbon content of 1.4% by weight and a nitrogen content of 0.8% by weight.
  • Table 3 Table 3:
  • Example 2b shows that carbon and nitrogen deposits can not be completely removed from the deactivated Raney cobalt catalyst by treatment with aqueous ammonia (Table 3).
  • the regeneration with aqueous sodium hydroxide solution or aqueous ammonia has the disadvantage that, in comparison to regeneration with anhydrous liquid ammonia, the water and the sodium hydroxide solution must first be completely removed because of the water sensitivity of EDDN. This leads to longer shutdown times.
  • the hydrogenation in the presence of the anhydrous ammonia can be taken directly into operation without ejecting it before. After commissioning, the ammonia is gradually discharged with the product. This results in a time advantage.

Landscapes

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

Abstract

Procédé de régénération de catalyseurs de Raney, comprenant le traitement du catalyseur avec de l'ammoniac liquide présentant une teneur en eau inférieure à 5% en poids, et de l'hydrogène à une pression partielle de 0,1 à 40 MPa, dans une plage de température comprise entre 50 et 350°C, pendant au moins 0,1 heure.
PCT/EP2012/066640 2011-08-31 2012-08-28 Procédé de régénération de catalyseurs de raney Ceased WO2013030172A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP11179624.9 2011-08-31
EP11179624 2011-08-31

Publications (1)

Publication Number Publication Date
WO2013030172A1 true WO2013030172A1 (fr) 2013-03-07

Family

ID=46754450

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2012/066640 Ceased WO2013030172A1 (fr) 2011-08-31 2012-08-28 Procédé de régénération de catalyseurs de raney

Country Status (1)

Country Link
WO (1) WO2013030172A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8981093B2 (en) 2012-06-06 2015-03-17 Basf Se Process for preparing piperazine
CN119327521A (zh) * 2023-07-17 2025-01-21 中国石油化工股份有限公司 活泼金属催化剂原位活性恢复的方法及其装置和应用

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3896051A (en) * 1972-12-25 1975-07-22 Toyo Soda Mfg Co Ltd Method of reactivation of raney nickel
DE19614283A1 (de) * 1996-04-11 1997-10-16 Basf Ag Verfahren zur Herstellung von Aminen und Aminonitrilen
WO1999033561A1 (fr) 1997-12-29 1999-07-08 Rhodia Fiber And Resin Intermediates Procede de regeneration d'un catalyseur d'hydrogenation procede d'hydrogenation de composes comprenant des fonctions nitriles
EP1209146A1 (fr) 2000-11-16 2002-05-29 Basf Aktiengesellschaft Procédé d'hydrogenation de nitriles en amines primaires utilisant des catalyseurs de Raney
WO2008104578A1 (fr) 2007-03-01 2008-09-04 Basf Se Procédé de fabrication d'éthylénamines à partir d'aan brut
WO2008104553A1 (fr) 2007-03-01 2008-09-04 Basf Se Procédé de fabrication de triéthylène-tétraamine
WO2008104579A1 (fr) 2007-03-01 2008-09-04 Basf Se Procédé de fabrication d'éthylène-diamine-diacétonitrile
WO2008104583A1 (fr) 2007-03-01 2008-09-04 Basf Se Procédé de préparation d'éthylène amines

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3896051A (en) * 1972-12-25 1975-07-22 Toyo Soda Mfg Co Ltd Method of reactivation of raney nickel
DE19614283A1 (de) * 1996-04-11 1997-10-16 Basf Ag Verfahren zur Herstellung von Aminen und Aminonitrilen
EP0892777A1 (fr) 1996-04-11 1999-01-27 Basf Aktiengesellschaft Procede de fabrication d'amines et d'aminonitriles
WO1999033561A1 (fr) 1997-12-29 1999-07-08 Rhodia Fiber And Resin Intermediates Procede de regeneration d'un catalyseur d'hydrogenation procede d'hydrogenation de composes comprenant des fonctions nitriles
EP1209146A1 (fr) 2000-11-16 2002-05-29 Basf Aktiengesellschaft Procédé d'hydrogenation de nitriles en amines primaires utilisant des catalyseurs de Raney
WO2008104578A1 (fr) 2007-03-01 2008-09-04 Basf Se Procédé de fabrication d'éthylénamines à partir d'aan brut
WO2008104553A1 (fr) 2007-03-01 2008-09-04 Basf Se Procédé de fabrication de triéthylène-tétraamine
WO2008104579A1 (fr) 2007-03-01 2008-09-04 Basf Se Procédé de fabrication d'éthylène-diamine-diacétonitrile
WO2008104583A1 (fr) 2007-03-01 2008-09-04 Basf Se Procédé de préparation d'éthylène amines

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"Ullmann's Encyclopedia of Industrial Chemistry", 15 June 2000, article "Amines, Aliphatic"
GÜNTHER REUSS; WALTER DISTELDORF; ARMIN OTTO GAMER; ALBRECHT HILT: "Ullmann's Encyclopedia of Industrial Chemistry", 15 June 2000, article "Formaldehyde", pages: 28

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8981093B2 (en) 2012-06-06 2015-03-17 Basf Se Process for preparing piperazine
CN119327521A (zh) * 2023-07-17 2025-01-21 中国石油化工股份有限公司 活泼金属催化剂原位活性恢复的方法及其装置和应用

Similar Documents

Publication Publication Date Title
EP2537835B1 (fr) Nouveau procédé destiné à la fabrication de TETA par EDDN
EP3700883B1 (fr) Procédé de fabrication d'éthylèneamines
EP3700884B1 (fr) Procede de production d'ethyleneamines
EP2961731B1 (fr) Procédé de production d'éthylène diamine en utilisant de l'acide prussique dépourvu de so2
WO2013030249A1 (fr) Procédé pour produire des amines par hydratation de nitriles
EP2443088A1 (fr) Composés teta à substitution méthyle
EP2751067A1 (fr) Procédé pour traiter des produits réactionnels issus de l'hydrogénation de eddn ou edmn
EP2751068A1 (fr) Procédé de préparation de eddn et/ou edmn par réaction de fach et eda
WO2013030259A1 (fr) Procédé de préparation de teta
EP2751066A1 (fr) Procédé de production de edfa et/ou edmfa, et deta et/ou teta
EP2751069B1 (fr) Procédé de production d'eddn et/ou d'edmn
WO2013030172A1 (fr) Procédé de régénération de catalyseurs de raney
EP2751065B1 (fr) Procédé de fabrication d'eddn et/ou edmn par conversion d'edfa et/ou edmfa avec hcn
WO2013030023A1 (fr) Procédé pour la production d'eddn et/ou d'edmn ainsi que procédé pour la production de deta et/ou de teta
WO2013030255A1 (fr) Procédé de préparation de eddn et/ou de edmn et procédé de préparation de deta et/ou de teta
WO2013030144A1 (fr) Procédé pour produire de l'eddn, de l'edmn, de la teta et de la deta
EP2412698B1 (fr) DMAPN ayant une teneur réduite en DGN et procédé de fabrication de DMAPA à partir de DMAPN ayant une teneur réduite en DGN
WO2013030254A1 (fr) Procédé pour produire teta et/ou deta
US20130085286A1 (en) Unknown
US9012638B2 (en) Process for preparing EDDN and/or EDMN by conversion of FACH and EDA
US20130053540A1 (en) Process for preparing teta
US20130053536A1 (en) Process for preparing eddn and/or edmn and a process for preparing deta and/or teta
US9096497B2 (en) Process for preparing EDDN and EDMN
US8946459B2 (en) Process for preparing EDDN and/or EDMN by reacting EDFA and/or EDMFA with HCN
US20130053537A1 (en) Process for regenerating raney catalysts

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 12751336

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 12751336

Country of ref document: EP

Kind code of ref document: A1