WO2011003932A2 - Procédé d'amination directe d'hydrocarbures en amino-hydrocarbures avec séparation électrochimique d'hydrogène - Google Patents

Procédé d'amination directe d'hydrocarbures en amino-hydrocarbures avec séparation électrochimique d'hydrogène Download PDF

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WO2011003932A2
WO2011003932A2 PCT/EP2010/059709 EP2010059709W WO2011003932A2 WO 2011003932 A2 WO2011003932 A2 WO 2011003932A2 EP 2010059709 W EP2010059709 W EP 2010059709W WO 2011003932 A2 WO2011003932 A2 WO 2011003932A2
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hydrogen
membrane
hydrocarbon
hydrocarbons
amination
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PCT/EP2010/059709
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German (de)
English (en)
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WO2011003932A3 (fr
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Petr Kubanek
Alexander Panchenko
Andreas Fischer
Thomas Heidemann
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Basf Se
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
    • B01D53/229—Integrated processes (Diffusion and at least one other process, e.g. adsorption, absorption)
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00—Electrolytic production of organic compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2256/00—Main component in the product gas stream after treatment
    • B01D2256/16—Hydrogen

Definitions

  • the present invention relates to a process for the direct amination of hydrocarbons with an aminating reagent to aminocarbons in the presence of a catalyst, wherein at least a portion of the resulting hydrogen in the reaction is separated by electrochemical means of a gas-tight membrane electrode assembly.
  • One possibility is to separate off part of the hydrogen from the reaction mixture of the direct amination, which contains amino hydrocarbon, unreacted starting materials and hydrogen, and to reuse the unreacted starting materials in the direct amination reaction.
  • the separation of the hydrogen from the reaction mixture is necessary, since otherwise the hydrogen shifts the thermodynamic equilibrium in the direction of the educts, thereby increasing the yield Aminohydrocarbon is even lower at the renewed Trimamintechnik.
  • Another possibility is to remove the hydrogen formed in the direct amination directly from the reaction zone. To remove the hydrogen from the reaction mixture, several methods are described.
  • WO 2007/096297 and WO 2000/69804 describe a process for the direct amination of aromatic hydrocarbons to give the corresponding aminocarbons, the resulting hydrogen being removed from the reaction mixture by oxidation on reducible metal oxides.
  • These processes have the disadvantage that the reducible metal oxides have to be regenerated with oxygen again after some time. This means costly interruptions of the process, since the direct amination of the hydrocarbons and the regeneration of the reducible metal oxides usually do not take place under the same conditions. For regeneration of the catalyst, the reactor must therefore usually be relaxed, rinsed and rendered inert.
  • WO 2007/099028 describes a direct amination of aromatic hydrocarbons to the corresponding amino hydrocarbons, wherein in a first step, the heterogeneously catalyzed Sparamintechnik is carried out and in a second step, the resulting hydrogen in the first step by reacting with an oxidizing agent such as air, oxygen, CO , CO 2 , NO and / or N 2 O is reacted.
  • an oxidizing agent such as air, oxygen, CO , CO 2 , NO and / or N 2 O is reacted.
  • oxidants such as oxygen leads to the oxidation of ammonia and the formation of further by-products. This leads to higher material costs and additional processing steps, whereby the economic efficiency of the process is deteriorated.
  • WO 2008/009668 also describes a process for the direct amination of aromatic hydrocarbons.
  • the removal of the hydrogen from the reaction mixture is achieved here by the directamination with the addition of is carried out, which react with the hydrogen formed in the direct amination.
  • Examples of compounds added to the direct amination are nitrobenzene and carbon monoxide. Also in this method, the disadvantages described above occur.
  • WO 2007/025882 describes the direct amination of aromatic hydrocarbons to the corresponding amino hydrocarbons, wherein hydrogen is physically separated from the reaction mixture.
  • the separation takes place here by a selectively hydrogen-permeable membrane, that is, hydrogen migrates as H 2 molecule through the membrane.
  • Palladium and palladium alloys are preferably used as membrane materials.
  • the diffusion rate in this process depends on the partial pressure difference of the hydrogen between the retentate and permeate sides of the membrane. In order to achieve higher diffusion rates, it is necessary to work at higher pressure differences, which place high demands on the mechanical stability of the membrane.
  • 51, 107- 122 is described in addition to temperatures above 300 0 C are required to achieve a sufficiently high diffusion rate.
  • appropriate devices for compressing and expanding the gas mixture must be present to form the pressure differences.
  • a certain proportion of the hydrogen always remains in the retentate. This has a negative effect on the position of the thermodynamic equilibrium.
  • the object of the present invention is therefore to provide a process for the direct amination of hydrocarbons to amino hydrocarbons, in which hydrogen is separated from the reaction mixture as effectively as possible, and that avoids the above-mentioned disadvantages of the prior art processes for Maisamintechnik.
  • the method should allow a shift in the position of the thermodynamic equilibrium on the side of Aminokohlenwas- substances.
  • the separation of the hydrogen should be made possible directly from the reaction zone.
  • the hydrocarbons used should be used efficiently as well as the by-products obtained during the reaction.
  • the method should have the best possible energy balance and the lowest possible expenditure on equipment.
  • the object is achieved according to the invention by a process for the direct amination of hydrocarbons to aminohydrocarbons by reacting a feed stream E which contains at least one hydrocarbon and at least one amination reagent to form a reaction mixture R containing amino alcohols.
  • the inventive method Compared with the known processes, in which the hydrogen is removed by reducible metal oxides, the inventive method has the advantage that costly and costly interruptions of the process for Maisaminie- tion are avoided and that the process can be operated continuously over a longer period.
  • the inventive method also comes in comparison to known methods in which gaseous oxidizing agents such as air, oxygen, CO, CO 2 , NO or N 2 O or compounds such as nitrobenzene are used without a complex apparatus and costly separation of the resulting by the addition of the oxidants by-products out.
  • the process of the invention has a particular advantage over the known processes in which hydrogen is separated as H 2 molecule by means of a hydrogen-selective membrane. This particular advantage lies in the electrochemical separation of the hydrogen formed from the reaction mixture R.
  • the driving force of electrochemical hydrogen separation is the potential difference between the two sides of the membrane. Since the separation is not dependent on the partial pressure difference of the hydrogen between the two sides of the membrane, as in the commonly used hydrogen-selective membranes, the hydrogen separation can be carried out at much lower pressures and pressure differentials, preferably to an externally impressed pressure difference can be omitted and especially on permeate and Retentatseite the same pressure prevails. This significantly reduces the mechanical stress on the membrane, which, among other things, increases its long-term stability and increases the choice of materials that can be used for the membrane.
  • the electrochemical separation of the hydrogen is significantly more effective compared to the separation by means of conventional hydrogen-selective membranes. With the same separation performance, therefore, the required membrane area can be reduced or significantly more hydrogen can be separated while the membrane area remains the same. the. Overall, therefore, the method according to the invention is associated with a lower expenditure on equipment.
  • the process according to the invention has the advantage that the hydrogen formed in the directamination and in the unavoidable decomposition of ammonia is recovered by separation from the reaction mixture.
  • the resulting in the process according to the invention hydrogen has a high purity and can be collected and sold or used for energy production. Due to the high purity of the hydrogen can be used as starting material in subsequent reactions, especially in those that react sensitively to impurities. In the following the invention will be described in detail.
  • the feedstock stream E contains at least one hydrocarbon.
  • Suitable hydrocarbons which can be used in the process according to the invention are, for example, hydrocarbons, such as aromatic hydrocarbons, aliphatic hydrocarbons and cycloaliphatic hydrocarbons, which may be arbitrarily substituted and heteroatoms and double or triple bonds within their chain or their ring (s) can have.
  • Aromatic hydrocarbons and heteroaromatic hydrocarbons are preferably used in the amination process according to the invention.
  • Suitable aromatic hydrocarbons are, for example, unsaturated cyclic hydrocarbons which have one or more rings and contain only aromatic C-H bonds.
  • Preferred aromatic hydrocarbons have one or more 5- and / or 6-membered rings.
  • a heteroaromatic hydrocarbon are meant those aromatic hydrocarbons in which one or more of the carbon atoms of the aromatic ring is replaced by a heteroatom selected from N, O and S.
  • the aromatic hydrocarbons or the heteroaromatic hydrocarbons may be substituted or unsubstituted.
  • a substituted aromatic or heteroaromatic hydrocarbon are meant compounds in which one or more hydrogen atoms bound to a carbon and / or heteroatom of the aromatic ring is / are replaced by another radical.
  • Suitable radicals are, for example, substituted or unsubstituted alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, cycloalkyl and / or cycloalkynyl radicals; Halogen, hydroxy, alkoxy, aryloxy, amino, amido, thio and phosphino.
  • Preferred radicals of the aromatic or heteroaromatic hydrocarbons are selected from Ci -6 alkyl, Ci -6 alkenyl, Ci -6 alkynyl, C 3-8 cycloalkyl, C 3-8 - cycloalkenyl, alkoxy, aryloxy, amino and amido where the indication Ci_6 refers to the number of carbon atoms in the main chain of the alkyl radical, the alkenyl radical or the alkynyl radical and the designation C 3-8 to the number of carbon atoms of the cycloalkyl or cycloalkenyl ring. It is also possible that the substituents (radicals) of the substituted aromatic or heteroaromatic hydrocarbon themselves have further substituents.
  • the number of substituents (radicals) of the aromatic or heteroaromatic hydrocarbon is arbitrary. In a preferred embodiment, however, the aromatic or heteroaromatic hydrocarbon has at least one hydrogen atom which is bonded directly to a carbon atom or a heteroatom of the aromatic or heteroaromatic ring.
  • a 6-membered ring preferably has 5 or fewer substituents (groups) and a 5-membered ring preferably has 4 or fewer substituents (groups).
  • a 6-membered aromatic or heteroaromatic ring carries 4 or fewer substituents, very particularly preferably 3 or fewer substituents (radicals).
  • a 5-membered aromatic or heteroaromatic ring preferably carries 3 or fewer substituents (radicals), more preferably 2 or fewer substituents (radicals).
  • A is independently aryl or heteroaryl, A is preferably selected from among phenyl, diphenyl, benzyl, dibenzyl, naphthyl, anthracene, pyridyl and quinoline; n is a number from 0 to 5, preferably 0 to 4, especially in the case when A is a
  • n is preferably 0 to 4; independently of the ring size, n is more preferably 0 to 3, most preferably 0 to 2 and especially 0 to 1; the other hydrocarbon substituents or heteroatoms of A carrying no substituents B carry hydrogen atoms or optionally no substituents;
  • B is independently selected from the group consisting of alkyl, alkenyl, alkynyl, substituted alkyl, substituted alkenyl, substituted alkynyl, heteroalkyl, substituted heteroalkyl, heteroalkenyl, substituted heteroalkenyl, heteroalkynyl, substituted heteroalkynyl, cycloalkyl, cycloalkenyl, substituted cycloalkyl , substituted cycloalkenyl, halogen, hydroxy, alkoxy, aryloxy, carbonyl, amino, amido, thio and phosphino; B is preferably independently of each other selected from C- ⁇ - 6 alkyl, d- 6 alkenyl, d- ⁇ -alkynyl,
  • Alkyl in the present application means branched or unbranched, saturated acyclic hydrocarbon radicals. Preference is given to using alkyl radicals having 1 to 20 carbon atoms, particularly preferably having 1 to 6 carbon atoms and in particular having 1 to 4 carbon atoms. Examples of suitable alkyl radicals are methyl, ethyl, n-propyl, i-propyl, n-butyl, t-butyl and i-butyl.
  • Alkenyl according to the present application is to be understood as meaning branched or unbranched acyclic hydrocarbon radicals which have at least one carbon-carbon double bond.
  • the alkenyl radicals preferably have 2 to 20 carbon atoms, particularly preferably 2 to 6 carbon atoms and in particular 2 to 3 carbon atoms. Suitable alkenyl radicals are, for example, vinyl and 2-propenyl.
  • Alkynyl according to the present application is to be understood as meaning branched or unbranched acyclic hydrocarbon radicals which have at least one carbon-carbon triple bond.
  • the alkynyl radicals preferably have 2 to 20 carbon atoms, particularly preferably 1 to 6 carbon atoms and in particular 2 to 3 carbon atoms. Examples of suitable alkynyl radicals are ethynyl and 2-propynyl.
  • Substituted alkyl, substituted alkenyl and substituted alkynyl are alkyl-alkenyl and alkynyl radicals in which one or more hydrogen atoms bound to one carbon atom of these radicals are replaced by another group.
  • Examples of such other groups are halogen, aryl, substituted aryl, cycloalkyl, cycloalkenyl, substituted cycloalkyl, substituted cycloalkenyl and combinations thereof.
  • suitable substituted alkyl radicals are benzyl and trifluoromethyl.
  • heteroalkyl, heteroalkenyl and heteroalkynyl are meant alkyl-alkenyl and alkynyl radicals wherein one or more of the carbon atoms in the carbon chain is replaced by a heteroatom selected from N, O and S.
  • the bond between the heteroatom and another carbon atom may be saturated or unsaturated.
  • Cycloalkyl according to the present application is to be understood as meaning saturated cyclic nonaromatic hydrocarbon radicals which are composed of a single ring or several condensed rings.
  • the cycloalkyl radicals have between 3 and 8 carbon atoms and more preferably between 3 and 6 carbon atoms.
  • Suitable cycloalkyl radicals are, for example, cycloproyol, cyclopentyl, cyclohexyl, cyclooctanyl and bicyclooctyl.
  • cycloalkenyl By cycloalkenyl, according to the present application, partially unsaturated, cyclic non-aromatic hydrocarbon radicals are to be understood which have a single or multiple condensed rings.
  • the cycloalkenyl radicals preferably have 3 to 8 carbon atoms and particularly preferably 5 to 6 carbon atoms.
  • Suitable cycloalkenyl radicals are, for example, cyclopentenyl, cyclohexenyl and cyclooctenyl.
  • Substituted cycloalkyl and substituted cycloalkenyl radicals are cycloalkyl and cycloalkenyl radicals wherein one or more hydrogen atoms of one carbon atom of the carbon ring are replaced by another group.
  • Such other groups are, for example, halogen, alkyl, alkenyl, alkynyl, substituted alkyl, substituted alkenyl, nyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, cycloalkenyl, substituted cycloalkyl, substituted cycloalkenyl, an aliphatic heterocyclic radical, a substituted aliphatic heterocyclic radical, heteroaryl, substituted heteroaryl, alkoxy, aryloxy, boryl, phosphino, amino, silyl, thio, Seleno and combinations of it.
  • substituted cycloalkyl and cycloalkenyl radicals are 4-dimethylaminocyclohexyl and 4,5-dibromocyclohept-4-enyl.
  • aryl is to be understood as meaning aromatic radicals which have a single aromatic ring or several aromatic rings which are condensed, linked via a covalent bond or by a linking unit such as a methylene or ethylene unit.
  • linking moieties may also be carbonyl moieties, such as in benzophenone, or oxygen moieties, such as in diphenyl ether, or nitrogen moieties, such as in diphenylamine.
  • the aryl radicals have 6 to 20 carbon atoms, more preferably 6 to 8 carbon atoms and most preferably 6 carbon atoms.
  • aromatic rings are phenyl, naphthyl, diphenyl, diphenyl ether, diphenylamine and benzophenone.
  • Substituted aryl radicals are aryl radicals in which one or more hydrogen atoms bound to carbon atoms of the aryl radical are replaced by one or more groups such as alkyl, alkenyl, alkynyl, substituted alkyl, substituted alkenyl, substituted alkynyl, cycloalkyl, cycloalkenyl, substituted cycloalkyl, substituted cycloalkenyl, heterocyclo, substituted heterocyclo, halogen, halo-substituted alkyl (eg CF 3 ), hydroxy, amino, phosphino, alkoxy and thio.
  • groups such as alkyl, alkenyl, alkynyl, substituted alkyl, substituted alkenyl, substituted alkynyl, cycloalkyl, cycloalkenyl, substituted cycloalkyl, substituted cycloalkenyl, heterocyclo, substituted heterocyclo,
  • one or more hydrogen atoms attached to carbon atoms of the aryl group may be replaced by one or more groups such as saturated and / or unsaturated cyclic hydrocarbons which may be fused to the aromatic ring (s) be linked, or linked together by a suitable group.
  • Suitable groups are those described above.
  • Heterocyclo in the present application means a saturated, partially unsaturated or unsaturated cyclic radical in which one or more carbon atoms of the radical have been replaced by a heteroatom such as N, O or S.
  • heterocyclo radicals are piperazinyl, morpholinyl, tetrahydropyranyl, tetrahydrofuranyl, piperidinyl, pyrolidinyl, oxazolinyl, pyridyl, pyrazyl, pyridazyl, pyrimidyl.
  • Substituted heterocyclo radicals are those heterocyclo radicals in which one or more hydrogen atoms which are bonded to one of the ring atoms are substituted by one or more groups such as halogen, alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl , Alkoxy, aryloxy, boryl, phosphino, amino, SiIyI, thio, seleno are replaced.
  • Alkoxy radicals are radicals of the general formula -OZ 1 , where Z 1 is selected from alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl and SiIyI.
  • Suitable alkoxy radicals are, for example, methoxy, ethoxy, benzyloxy and t-butoxy.
  • aryloxy are meant those radicals of general formula -OZ 2 wherein Z 2 is selected from aryl, substituted aryl, heteroaryl, substituted heteroaryl and combinations thereof.
  • Suitable aryloxy radicals and heteroaryloxy radicals are phenoxy, substituted phenoxy, 2-pyridinoxy and 8-quinolinoxy.
  • Amino radicals are radicals of the general formula -NZ 3 Z 4 in which Z 3 and Z 4 are selected independently of one another from hydrogen, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl, aryl, substituted aryl, Heteroaryl, substituted heteroaryl, alkoxy, aryloxy and SiIyI.
  • Preferred aromatic and heteroaromatic hydrocarbons used in the amination process according to the invention are benzene, naphthalene, diphenylmethanes, anthracene, toluene, xylene, phenol and aniline and also pyridine, pyrazine, pyridazine, pyrimidine and quinoline.
  • At least one hydrocarbon from the group of benzene, naphthalene, diphenylmethane, anthracene, toluene, xylene, phenol and aniline and also pyridine, pyrazine, pyridazine, pyrimidine and quinoline is used. It is also possible to use mixtures of said aromatic or heteroaromatic hydrocarbons. Particular preference is given to using at least one aromatic hydrocarbon from the group consisting of benzene, naphthalene, anthracene, toluene, xylene, phenol and aniline, very particularly preferably benzene, toluene and naphthalene. Benzene is particularly preferably used in the process according to the invention.
  • methane is particularly preferred for use in the process of the present invention.
  • the feedstock stream E contains at least one amination reagent.
  • Suitable aminating reagents are those by which at least one amino group is introduced into the hydrocarbon used for direct amination.
  • Examples of preferred aminating reagents are ammonia, primary and secondary amines and compounds which split off ammonia under the reaction conditions. It is also possible to use mixtures of two or more of the abovementioned amination reagents.
  • preferred amination reagent is ammonia
  • a reactant stream E which comprises at least one hydrocarbon and at least one aminating reagent is converted to a reaction mixture R which contains at least one amino hydrocarbon and hydrogen.
  • at least one amino hydrocarbon corresponding to the hydrocarbon used is obtained which contains at least one amino group more than the hydrocarbon used.
  • aminohydrocarbon is therefore to be understood as meaning the reaction product of the hydrocarbons used in the process with the aminating reagent.
  • at least one amino group is transferred from the aminating reagent to the carbohydrate.
  • 1 to 6 amino groups in a particularly preferred embodiment 1 to 3 amino groups, very particularly preferably 1 to 2 amino groups and particularly preferably 1 amino group are transferred to the hydrocarbon.
  • the number of amino groups transferred can be controlled by the molar ratio of amination reagent to aminierendem hydrocarbon and by the reaction temperature.
  • the ratio of amination reagent to hydrocarbon is 0.5 to 9, preferably 1 to 5, particularly preferably 1, 5 to 3.
  • ammonia in a molar ratio in the range of 1 to 9 are used in the process according to the invention as the hydrocarbon benzene and as the amination reagent, is obtained as the amino hydrocarbon aniline.
  • toluene is used as the hydrocarbon in the process according to the invention and ammonia in the molar ratio in the range from 1 to 9 is used as the aminating reagent, toluene diamine is obtained as the aminohydrocarbons.
  • methane is used in the process according to the invention as the hydrocarbon and ammonia in a molar ratio in the range from 1 to 9 as the aminating reagent
  • methylamine, dimethylamine or trimethylamine or a mixture of two or more of the abovementioned amines is obtained as aminohydrocarbyl
  • benzene is reacted with ammonia to aniline.
  • toluene is reacted with ammonia to form toluenediamine.
  • the direct amination is carried out in the presence of at least one catalyst.
  • catalysts in principle, all known amination catalysts are suitable. Suitable catalysts for the direct amination of hydrocarbons, in particular those known for the direct amination of benzene with ammonia to aniline catalysts can be used. Such catalysts are described in the patent literature, for example, in WO 2007/099028, WO 2007/096297, WO 2000/69804, WO 2008/009668, WO 2007/025882, US Pat. No. 3,919,155, US Pat. No. 3,929,889, US Pat. No. 4,001,260, US Pat. No. 4,031,106, and US Pat WO 99/1031 1 described. Since, according to the process according to the invention, the removal of the hydrogen takes place electrochemically and not by chemical conversion in the reaction system, it is also possible to use catalysts which have no components which are reactive toward hydrogen.
  • customary metal catalysts based on nickel, iron, cobalt, copper, precious metals or alloys of these metals can be used as catalysts.
  • Preferred noble metals (EM) are Ru, Rh, Pd, Ag, Ir, Pt and Au.
  • the noble metals Ru and Rh are not used alone, but in alloy with one or more other transition metals, such as Co, Cu, Fe and nickel.
  • suitable catalysts are supported NiCuNM; CoCuEM; NiCoCuEM, NiMoEM, NiCrEM, NiReEM, CoMoEM, CoCrEM, Co-ReEM, FeCuEM, FeCoCuEM, FeMoEM, FeReEM alloys.
  • EM is a deliming metal, preferably Pt, Pd, Ag, Ir, particularly preferably Ag and / or Ir. Further particularly preferred is NiCuEM, wherein EM is selected from Pt, Pd, Ag and / or Ir.
  • the electrocatalyst (electrode) used on the retentate side simultaneously serves as a catalyst for the conversion of hydrocarbon to aminocarbon (amination catalyst).
  • the amination catalyst may be attached directly to the electrocatalyst. In this case, the hydrogen released in the reaction is discharged directly from the catalyst surface of the amination catalyst through the proton-conducting membrane.
  • the catalyst can be used in generally conventional form, for example as a powder or for use in a fixed bed in the form of strands, spheres, tablets or rings.
  • the catalytically active constituents can be present on a carrier material.
  • suitable carrier materials are inorganic oxides, for example ZrO 2 , SiO 2 , Al 2 O 3 , MgO, TiO 2 , B 2 O 3 , CaO, ZnO, BaO, ThO 2 , CeO 2 , Y 2 O 3 and mixtures of these oxides, such as magnesium aluminum oxide, preferably TiO 2 , ZrO 2 , Al 2 O 3 , magnesium aluminum oxide and SiO 2 into consideration. Particularly preferred are Al 2 O 3 , ZrO 2 and magnesium aluminum oxide.
  • ZrO 2 is understood as meaning both pure ZrO 2 and the normal Hf-containing ZrO 2 .
  • the catalysts preferably used in the process according to the invention can be regenerated, for example by passing a reductive atmosphere over the catalyst or by first passing an oxidative and then a reductive atmosphere over or through the catalyst bed.
  • a reductive atmosphere an H 2 atmosphere is preferably used.
  • the direct amination can be carried out under oxidative or non-oxidative conditions.
  • the direct amination can also be carried out under catalytic or non-catalytic conditions.
  • the directamination takes place in the presence of a catalyst under non-oxidative conditions.
  • Non-oxidative according to the present invention in relation to the direct amination means that the concentration of oxidizing agents such as oxygen or nitrogen oxides in the educts used (starting material flow E) is below 5% by weight, preferably below 1% by weight. particularly preferably below 0.1% by weight (in each case based on the total weight of the reactant stream E).
  • Educt stream E is understood in the context of the present invention to mean the stream which is conducted to the reactor and contains at least one hydrocarbon and at least one aminating reagent. Most preferably, the reactant stream E is free of oxygen. Also particularly preferred is a concentration of oxidant in the reactant stream E, which is equal to or less than the concentration of oxidizing agents in the source from which the hydrocarbons and aminating reagents used originate.
  • reaction conditions in the direct amination processes according to the invention depend inter alia on the hydrocarbon to be aminated and the catalyst used.
  • the direct amination is generally carried out at temperatures of 20 to 800 0 C, preferably 50 to 700 0 C, more preferably 70 to 350 0 C.
  • the reaction pressure in the direct lamination is preferably 0.5 to 40 bar, preferably 1 to 6 bar, especially preferably 1 to 3 bar, in particular atmospheric pressure.
  • the residence time in the case of discontinuous process control in the amination process according to the invention is generally from 15 minutes to 8 hours, preferably from 15 minutes to 4 hours, particularly preferably from 15 minutes to 1 hour.
  • the residence time is generally 0.1 second to 20 minutes, preferably 0.5 second to 10 minutes.
  • "residence time" in this context means the residence time of the reactant stream E on the catalyst, for fixed bed catalysts thus the residence time in the catalyst bed, for fluidized bed reactors, the synthesis part of the reactor is considered (part of the reactor where the catalyst is located).
  • the relative amount of the hydrocarbon used and of the amination reagent depends on the amination reaction carried out and the reaction conditions. Generally, at least stoichiometric amounts of the hydrocarbon and the amine reagent are used. Preferably, one of the reactants will be used in stoichiometric excess to achieve equilibrium shift to the desired product side and thus higher conversion. Preferably, the Aminn michsreagenz in stoichiometric Excess in relation to the hydrocarbon used.
  • the ratio of amination reagent to hydrocarbon is 0.5 to 9, preferably 1 to 5, more preferably 1, 5 to 3. Hydrogen separation:
  • reaction mixture R is understood to mean the mixture which is formed by the chemical reaction of at least one hydrocarbon with at least one amination reagent.
  • the reaction mixture therefore usually contains as reaction products the corresponding amino hydrocarbons and hydrogen.
  • the reaction mixture R may further contain unreacted starting materials.
  • the hydrogen is separated by means of a gas-tight membrane-electrode assembly, wherein the hydrogen to be separated is transported in the form of protons through the membrane. For the transport of the protons through the membrane electrical energy must be expended, which is supplied by applying a DC voltage to the two sides of the membrane by means of electrodes.
  • the electrodes with the membrane interposed therebetween are called Membrane Electrode Assembly (MEA).
  • MEA Membrane Electrode Assembly
  • the reaction mixture R is guided along one side of the membrane. This page is called retentate page below.
  • the permeate side On the other side of the membrane, hereinafter referred to as the permeate side, the separated hydrogen is removed.
  • the MEA has at least one selectively proton-conducting membrane.
  • the membrane has at least one electrode catalyst on each side, in the context of this description the electrode catalyst located on the retentate side being referred to as anode catalyst, and the electrode catalyst located on the permeate side as cathode catalyst.
  • the hydrogen on the anode catalyst is oxidized to protons, these pass through the membrane and are reduced to hydrogen on the permeate side of the cathode catalyst.
  • the hydrogen is separated directly from the reaction mixture R. Further preferably, the hydrogen is separated directly from the reaction zone RZ, in which the reaction mixture R is formed.
  • Reaction zone RZ in the context of the present invention is to be understood as the region in which the chemical reaction of at least one hydrocarbon and at least one aminating reagent takes place for the reaction mixture R.
  • the separation of hydrogen according to the inventive process may be from 0 C at temperatures of 20 to 800, are preferably carried out from 50 to 700 0 C, particularly preferably from 70 to 350 0 C.
  • the separation is carried out preferably at 130 to 200 0 C.
  • ceramic membranes for example based on ammonium polyphosphate, it is possible to work at temperatures of 250 to 350 ° C.
  • the separation of the hydrogen by the process according to the invention is preferably carried out at pressures of from 0.5 to 40 bar, preferably from 1 to 6 bar, more preferably from 1 to 3 bar, in particular at atmospheric pressure.
  • the pressure difference between the retentate and the permeate side of the membrane is below 1 bar, preferably below 0.5 bar, more preferably there is no pressure difference.
  • the separation of the hydrogen is brought about by the formation of a potential difference between the two sides of the membrane by applying a voltage according to the invention.
  • the separation is carried out at voltages from 0.05 to 2000 mV, preferably from 100 to 900 mV, particularly preferably from 100 to 800 mV, measured against a hydrogen reference electrode (RHE).
  • RHE hydrogen reference electrode
  • At least part of the hydrogen formed in the direct amination is separated off.
  • the hydrogen obtained on the permeate side contains at most 5 mol%, preferably at most 2 mol% and particularly preferably at most 1 mol% of hydrocarbons.
  • the hydrogen may contain up to 30 mol%, preferably up to 10 mol%, particularly preferably up to 2 mol%, of water, depending on the selectively proton-conducting membrane used. The presence of water is required with some types of membranes, for example, certain polymer membranes to moisten the polymer membrane.
  • the separation of the hydrogen from the reaction mixture R is carried out in a reactor which is equipped with at least one gas-tight MEA in such a way that the reaction zone RZ is on the retinal side of the membrane or forms.
  • the separation can be carried out in one embodiment. tion form, for example, in a reactor whose outer walls are at least partially formed of gas-tight MEAs performed.
  • the separated hydrogen can still be dried prior to further use, this is carried out in particular if the separation takes place through a polymer membrane which has to be moistened.
  • Reactors In the process according to the invention, it is possible to use all reactor types which are suitable for direct-lamination reactions and which have been modified by at least one gas-tight MEA.
  • Suitable reactors are thus tube reactors, fixed bed reactors, membrane reactors, fluidized bed reactors, moving beds, circulating fluidized beds, salt bath reactors, plate heat exchanger reactors, tray reactors with multiple trays with or without heat exchange or withdrawal / supply of partial flows between the trays, in possible embodiments as radial flow or axial flow reactors, wherein in each case the reactor suitable for the desired reaction conditions (such as temperature, pressure and residence time) is used.
  • the reactors can each be used as a single reactor, as a series of individual reactors and / or in the form of two or more parallel reactors.
  • the process according to the invention can be carried out as a semi-continuous reaction or a continuous reaction.
  • the specific reactor construction and the performance of the reaction can vary depending on the amination process to be carried out, the state of matter of the aromatic hydrocarbon to be aminated, the required reaction times and the nature of the catalyst used.
  • the process according to the invention for directamination is preferably carried out in a fixed bed reactor or fluidized bed reactor which has been modified according to the invention with at least one MEA.
  • electrode catalyst The function of electrode catalyst is z.
  • K.A. Perry, G.A. Eisman, B.C. Benicewicz described "electrochemical hydrogen pumping using a high-temperature polybenzimidazole (PBI) membrane".
  • the electrode layers are usually contacted with gas distribution layers. These are, for example, plates with a grid-like surface structure of a system of fine channels or layers of porous material such as fleece, fabric or paper.
  • gas distribution layers These are, for example, plates with a grid-like surface structure of a system of fine channels or layers of porous material such as fleece, fabric or paper.
  • the entirety of gas distributor layer and electrode layer is generally referred to as gas diffusion electrode (GDE).
  • GDE gas diffusion electrode
  • the anode can simultaneously serve as an anode catalyst and the cathode at the same time as a cathode catalyst.
  • the anode catalyst may also serve as an amination catalyst at the same time.
  • the anode catalyst is formed from at least one material of the abovementioned amination catalysts.
  • the customary materials known to the person skilled in the art can be used for producing the electrodes, for example Pt, Pd, Cu, Ni, Ru, Co, Cr, Fe, Mn, V, W, tungsten carbide, Mo, molybdenum carbide, Zr, Rh, Ag, Ir, Au, Re, Y, Nb, electrically conductive forms of carbon such as carbon black, graphite and nanotubes, and alloys and mixtures of the foregoing elements.
  • the anode and the cathode may be made of the same material or of different materials.
  • the anode catalyst and the cathode catalyst may be selected from the same or different materials. Particularly preferred as the anode / cathode combination are Pt / Pt, Pd / Pd, Pt / Pd, Pd / Pt, Pd / Cu, Pd / Ag, Ni / Pt, Ni / Ni and Fe / Fe.
  • electrode catalyst material it is possible to use the customary compounds known to the person skilled in the art and elements which can catalyze the dissociation of molecular hydrogen into atomic hydrogen, the oxidation of hydrogen into protons and the reduction of protons to hydrogen. Suitable examples are Pd, Pt, Cu, Ni, Ru, Fe, Co, Cr, Mn, V, W, tungsten carbide, Mo, molybdenum carbide, Zr, Rh, Ag, Ir, Au, Re, Y, Nb and alloys and mixtures of these, Pd, Pt and Ni are preferred according to the invention.
  • the above as electrode catalysis Tormaterial called elements and compounds may also be present in a supported, preferably carbon is used as a carrier.
  • carbon containing conductive material is preferably used.
  • the carbon and an electrode catalyst are preferably applied to a porous support such as fleece, fabric or paper.
  • the carbon can be mixed with the catalyst or first the carbon and then the catalyst can be applied.
  • the electrically conductive material used as electrode and the electrode catalyst is applied directly to the membrane.
  • the membrane is preferably formed as a plate or as a tube, wherein the usual, known from the prior art for the separation of gas mixtures membrane arrangements can be used, for example, tube bundle or plug-in membrane.
  • the MEA used in the invention is gas-tight, that is, it has virtually no porosity, can pass through the gases in atomic or molecular form from one side to the other side of the MEA, nor does it have mechanisms by the gases nonselectively, for example by adsorption, Solution in the membrane, diffusion and desorption can be transported through the MEA.
  • the tightness of the membrane-electrode assembly (MEA) can be ensured either by a gas-tight membrane, by a gas-tight electrode, or by a gas-tight electrode catalyst, and by a combination thereof.
  • a gas-tight electrode a thin metallic foil may be used, for example, a Pd, Pd-Ag or Pd-Cu foil.
  • the membrane used according to the invention selectively conducts protons, that is to say in particular that it is not electron-conducting.
  • the following ceramic membranes such as certain heteropolyacids such as H 3 Sb 3 B 2 O 4 • 10H 2 O, H 2 Ti 4 O 9 • 12H 2 O and HSbP 2 O 8 • 10 H 2 O; acidic zirconium silicates, phosphates and phosphonates in a layered structure such as K 2 ZrSi 3 O 9 , K 2 ZrSi 3 O 9 , alpha-Zr (HPO 4 ) 2 • nH 2 O, gamma-Zr (PO 4 ) - (H 2 PO 4 ) • 2H 2 O, alpha and gamma Zr sulfophenyl phosphonate or sulfoaryl phosphonate; non-layered oxide hydrates such as antimony acid (Sb 2 O 5 .2H 2 O), V 2 O 5 .nH 2 O, ZrO 2 .nH 2 O, SnO 2 .nH 2 O and Ce (HPO 4 ) 2
  • oxo acids and salts containing, for example, sulfate, selenate, phosphate, arsenate, nitrate groups, etc. can be used.
  • oxoanionic systems based on phosphates or complex heteropolyacids such as polyphosphate glasses, aluminum polyphosphate, ammonium polyphosphate and polyphosphate compositions such as NH 4 PO 3 / (NH 4 ) 2 SiP 4 Oi 3 and NH 4 PO 3 / TiP 2 O 7 .
  • oxidic materials can be used, such as brownmillerites, fluorites and phosphates with apatite structure, pyrochlore minerals and perovskites.
  • all proton-conducting materials such as zeolites, aluminosilicates, xAl 2 O 3 (1 -X) SiO 2 , SnP 2 O 7 ,
  • Perovskites have the basic formula AB 1-x M x O 3-y , where M is a trivalent rare earth element which serves for doping, and y is the oxygen deficiency in perovskite oxide.
  • A may be selected from Mg, Ca, Sr and Ba.
  • B can be selected from CeZr and Ti.
  • A, B and M different elements from the respective groups can also be selected independently of one another.
  • structurally modified glasses can be used, such as chalcogenide
  • Examples of proton-conducting ceramics and oxides are SrCeO 3 , BaCeO 3 , Yb: SrCeO 3 , Nd: BaCeO 3 , Gd: BaCeO 3 , Sm: BaCeO 3 , BaCaNdO 9 , Y: BaCeO 3 , Y: BaZrCeO 3 , Pr-doped Y BaCeO 3 , Gd: BaCeO 3 , BaCe 0 , 9 Y 0 , 10 2 , 95 (BYC), SrCe 0 , 95 Ybo, o5 ⁇ 3- ⁇ , BaCe 0 , 9 Ndo, 10-3 - ⁇ , CaZr 0196 In 01 O 4 O 3-0 , ( ⁇ denotes the number of oxygen vacancies per formula unit of the perovskite type oxide); Sr-doped La 3 P 3 O 9 , Sr-doped LaPO 4 ,
  • polymer membranes suitable for the preparation of gas tight and selectively proton conducting membranes.
  • Suitable polymers include sulfonated polyetheretherketone (S-PEEK), sulfonated polybenzoimidazoles (S-PBI) and sulfonated fluorocarbon polymers (NAFION ®).
  • perforated polysulfonic acids, styrene-based polymers, poly (arylene ethers), polyimides and polyphosphazenes can be used. It can be used that are based on polybenzimidazole and phosphoric acid, as sold for example under the name Celtec-P ® from BASF SE also Polybenzamidazolen.
  • the above-mentioned ceramic membranes are preferably used as materials for the selectively proton-conducting membrane.
  • polymer membranes When polymer membranes are used, they are usually moistened by the presence of about 0.5 to 30% by volume of water on at least one side of the membrane.
  • a product stream P is obtained.
  • This contains at least one amino hydrocarbon and optionally unreacted starting materials, such as hydrocarbons and aminating reagents, and optionally not separated hydrogen.
  • the product stream P contains less than 500, preferably less than 200, and particularly preferably less than 100 ppm of hydrogen.
  • further hydrogen can be separated from the product stream P.
  • the product stream P is brought into contact again with one or more MEAs in a subsequent step.
  • the separation of the hydrogen from the reaction mixture is so complete that a subsequent separation of hydrogen from the product stream P is not necessary.
  • the amino hydrocarbon and the amination reagent are separated from the product stream P.
  • the order of separation is freely selectable.
  • only the amination reagent and then the amino hydrocarbon is separated off.
  • the reclaimed stream S1 thus obtained contains the unreacted hydrocarbon. In a preferred embodiment, this is used again in the direct lamination.
  • the hydrocarbon from stream S1 is either added to the educt stream E or directly recycled to the reaction zone.
  • the separation of aminocarbon and Aminianssreagenz can be carried out according to well-known, familiar to the expert methods, for example by condensation, distillation or extraction.
  • the choice of the pressure and temperature range depends on the physical properties of the compounds to be separated and is known to the person skilled in the art.
  • the product stream P at 50 0 C to 250 0 C, preferably at 70 0 C to 200 0 C, particularly preferably at 80 0 C to 150 0 C, at pressures in the range of 0 to 5 bar, preferably 0.5 to 2 bar, more preferably 0.8 to 1, 5 bar and cooled in particular at atmospheric pressure.
  • the amino hydrocarbons condense, while unconverted hydrocarbon and amination reagent and optionally still present hydrogen in gaseous form and thus can be separated by conventional methods, for example with a gas-liquid separator.
  • the liquid components thus obtained contain the amino hydrocarbon and unreacted hydrocarbon, the separation of amino hydrocarbon and hydrocarbon also takes place by methods known in the art, such as distillation, rectification or acid extraction.
  • the amounts of hydrocarbon and amination reagent added to recycled recycle stream S1 are selected to maintain the molar ratios of hydrocarbon and amination reagent required for the direct amination.
  • the product stream P contains essentially aniline, unreacted benzene and ammonia, and optionally byproducts and residues of hydrogen.
  • the product stream P is first separated by condensation into a gaseous phase containing ammonia and optionally hydrogen radicals, and a liquid phase containing aniline and benzene.
  • the liquid phase is subsequently separated by distillation, rectification or acid extraction in aniline and benzene.
  • the benzene (stream S1) is reused in the direct lamination. That so optionally obtained aniline may be subjected to further work-up steps.
  • the product stream P is used again in the direct lamination.
  • the product stream P can be admixed with the Edutkstrom E or introduced separately directly into the reaction zone RZ.
  • the product stream P is fed back as long as in the reaction zone RZ until the product stream P has enriched a concentration of amino hydrocarbon, which allows economical processing.
  • the product stream P is preferably recycled one to twenty times, preferably one to ten times, more preferably one to five times, and particularly preferably one to three times, to the reaction zone RZ.
  • the amounts of hydrocarbon and amination reagent added to the recycled product stream P are selected such that the MoI ratios of hydrocarbon and amination reagent required for the directamination are maintained.
  • the work-up and separation of the amino hydrocarbon takes place according to the method described under variant I.
  • the aminohydrocarbyl is separated from the product stream P.
  • the reclaimed stream S2 obtained in this process variant contains unconverted hydrocarbon and amination reagent.
  • This reclaimed stream S2 can be reused in direct lamination.
  • the worked-up product stream can be admixed with the educt stream E or introduced directly into the reaction zone RZ.
  • the separation of the amino hydrocarbon takes place by methods known to those skilled in the art, for example by condensation, distillation or acid extraction.
  • the aminohydrocarbyl is preferably removed from the product stream P by acid extraction.
  • the amounts of hydrocarbon and amination reagent added to the recycled product stream P are selected such that the molar ratios of hydrocarbon and amination reagent required for the directamination are maintained.
  • benzene and ammonia (reactant stream E) are added at a temperature of 300-350 0 C.
  • the cell contains a gas-tight MEA with sufficient active area.
  • the proton-conducting membrane of the MEA is ammonium polyphosphate.
  • electrodes of the MEA gas diffusion electrodes ELAT (1 mg / cm 2 platinum) from BASF Fuel Cell GmbH are used both for the anode and for the cathode.
  • an amination catalyst made of a carbon fabric containing finely dispersed NiCu alloy (about 3-5 mg / cm 2 ) is incorporated on the retentate side of the electric cell, this catalyst layer is attached directly to the ELAT gas diffusion electrode.
  • the MEA therefore has a layer structure with - starting on the retentate side - the following layer sequence:
  • Amination catalyst comprising a carbon fabric containing finely dispersed NiCu alloy (about 3 to 5 mg / cm 2 ),
  • Pd film is gas-tight and thus offers protection of the ceramic membrane from ammonia.
  • an amination catalyst made of a carbon fabric containing finely dispersed NiCu alloy (about 3-5 mg / cm 2 ) is incorporated on the retentate side of the electric cell, this catalyst layer is attached directly to the Pd film.
  • the MEA therefore has a layer structure with - starting on the retentate side - the following layer sequence:
  • Amination catalyst comprising a carbon fabric containing finely dispersed NiCu alloy (about 3 to 5 mg / cm 2 ),
  • a voltage (U A ) in the range of +250 to +800 mV is applied.
  • the hydrogen is oxidized to protons on the retentate side at the anode, these pass through the membrane and are reduced to hydrogen at the cathode.
  • the reactor discharge is a mixture of benzene, aniline, hydrogen, nitrogen and ammonia. Much of the hydrogen is separated from the reaction mixture R directly from the reaction zone by means of the electromembrane and thus the equilibrium conversion of benzene to aniline is increased.

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Abstract

L'invention concerne un procédé d'amination directe d'hydrocarbures en amino-hydrocarbures par transformation d'un flux de produit de départ (E) contenant au moins un hydrocarbure et au moins un réactif d'amination, en mélange de réaction (R) contenant des amino-hydrocarbures et de l'hydrogène dans une zone de réaction (RZ), et séparation électrochimique d'au moins une partie de l'hydrogène produit lors de la transformation, contenu dans le mélange de réaction (R), au moyen d'un ensemble membrane-électrode étanche aux gaz, présentant au moins une membrane guidant sélectivement les protons, et sur chaque côté de la membrane, au moins un catalyseur d'électrode. Sur le côté du rétentat de la membrane, au moins une partie de l'hydrogène est oxydé sous forme de protons sur le catalyseur d'anode, et après passage de la membrane, les protons sont réduits sous forme d'hydrogène sur le catalyseur de cathode, sur le côté du perméat.
PCT/EP2010/059709 2009-07-10 2010-07-07 Procédé d'amination directe d'hydrocarbures en amino-hydrocarbures avec séparation électrochimique d'hydrogène WO2011003932A2 (fr)

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WO2013131723A1 (fr) 2012-03-06 2013-09-12 Basf Se Procédé de préparation d'amino-hydrocarbures par amination directe d'hydrocarbures
WO2013131864A1 (fr) 2012-03-06 2013-09-12 Basf Se Procédé de préparation d'amino-hydrocarbures par amination directe d'hydrocarbures
US8642810B2 (en) 2009-07-10 2014-02-04 Basf Se Method for the direct amination of hydrocarbons into amino hydrocarbons, including electrochemical separation of hydrogen and electrochemical reaction of the hydrogen into water
US9061961B2 (en) 2009-07-10 2015-06-23 Basf Se Method for direct amination of hydrocarbons to form amino hydrocarbons with the electrochemical separation of hydrocarbon
US11351149B2 (en) 2020-09-03 2022-06-07 Pfizer Inc. Nitrile-containing antiviral compounds

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8642810B2 (en) 2009-07-10 2014-02-04 Basf Se Method for the direct amination of hydrocarbons into amino hydrocarbons, including electrochemical separation of hydrogen and electrochemical reaction of the hydrogen into water
US9061961B2 (en) 2009-07-10 2015-06-23 Basf Se Method for direct amination of hydrocarbons to form amino hydrocarbons with the electrochemical separation of hydrocarbon
WO2013131723A1 (fr) 2012-03-06 2013-09-12 Basf Se Procédé de préparation d'amino-hydrocarbures par amination directe d'hydrocarbures
WO2013131864A1 (fr) 2012-03-06 2013-09-12 Basf Se Procédé de préparation d'amino-hydrocarbures par amination directe d'hydrocarbures
US11351149B2 (en) 2020-09-03 2022-06-07 Pfizer Inc. Nitrile-containing antiviral compounds
US11452711B2 (en) 2020-09-03 2022-09-27 Pfizer Inc. Nitrile-containing antiviral compounds
US11541034B2 (en) 2020-09-03 2023-01-03 Pfizer Inc. Nitrile-containing antiviral compounds

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