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
  • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
  • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
  • B01J23/44—Palladium
• • 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
  • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
  • B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
  • B01J21/04—Alumina
• • 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
  • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
  • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
  • B01J23/42—Platinum
• • 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
  • B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
  • B01J23/892—Nickel and noble metals
• • 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
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
  • B01J35/391—Physical properties of the active metal ingredient
  • B01J35/394—Metal dispersion value, e.g. percentage or fraction
• • 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
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
  • B01J35/396—Distribution of the active metal ingredient
  • B01J35/397—Egg shell like
• • 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
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/40—Catalysts, in general, characterised by their form or physical properties characterised by dimensions, e.g. grain size
• • 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
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/50—Catalysts, in general, characterised by their form or physical properties characterised by their shape or configuration
  • B01J35/51—Spheres
• • 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
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J35/61—Surface area
  • B01J35/613—10-100 m2/g
• • 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
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J35/61—Surface area
  • B01J35/615—100-500 m2/g
• • 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
  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
  • B01J37/02—Impregnation, coating or precipitation
  • B01J37/0201—Impregnation
• • 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
  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
  • B01J37/02—Impregnation, coating or precipitation
  • B01J37/0236—Drying, e.g. preparing a suspension, adding a soluble salt and drying
• • 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
  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
  • B01J37/08—Heat treatment
  • B01J37/082—Decomposition and pyrolysis
  • B01J37/088—Decomposition of a metal salt
• • 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
  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
  • B01J37/16—Reducing
  • B01J37/18—Reducing with gases containing free hydrogen
• • 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
  • C07C11/00—Aliphatic unsaturated hydrocarbons
  • C07C11/02—Alkenes
  • C07C11/08—Alkenes with four carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
  • C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
  • C07C5/23—Rearrangement of carbon-to-carbon unsaturated bonds
  • C07C5/25—Migration of carbon-to-carbon double bonds
  • C07C5/2506—Catalytic processes
  • C07C5/2556—Catalytic processes with metals
• • 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
  • B01J23/90—Regeneration or reactivation
  • B01J23/96—Regeneration or reactivation of catalysts comprising metals, oxides or hydroxides of the noble metals
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
  • C07C2521/02—Boron or aluminium; Oxides or hydroxides thereof
  • C07C2521/04—Alumina
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
  • C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
  • C07C2523/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
  • C07C2523/44—Palladium
• • 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 palladium- or platinum-containing catalysts on an alumina support and to processes for the isomerization of olefins from olefin-containing hydrocarbon mixtures having 4 to 20 carbon atoms, in particular a process for the isomerization of 1-butene to 2-butene using this cata- - goals.
• Linear alpha-olefins in particular those having 4 to 8 C atoms, are used in petrochemical processes such as catalytic or thermal cracking, pyrolysis, dimerization, oligomerization or Fischer-Tropsch syntheses or as by-products of chemical processes such as methyl raffinates tert-butyl ether production or butadiene process.
• petrochemical processes such as catalytic or thermal cracking, pyrolysis, dimerization, oligomerization or Fischer-Tropsch syntheses or as by-products of chemical processes such as methyl raffinates tert-butyl ether production or butadiene process.
• the alpha-olefins thus obtained which have a terminal C-C double bond, must be rearranged by isomerization to the thermodynamically favored linear internal olefins having the same C atom number.
• these 4 to 8 carbon internal olefins can be incorporated into a metathesis reaction to produce other olefins, alkylated to produce gasoline, or reacted in other reactions to the desired products, for example, in electrophilic additions, dimerizations , Oligomerizations Co- and Polymerizations.
• EP 0 841 090 A2 describes a catalyst which is used for the isomerization of 3-buten-1-ol compounds.
• the fixed bed catalyst contains palladium and selenium or tellurium or a mixture of selenium and tellurium on a silica support and has a BET surface area of 80 to 380 m 2 / g and a pore volume of 0.6 to 0.95 cm 3 / g im Pore diameter range from 3 nm to 300 microns, with 80 to 95% of the pore volume in the pore diameter range of 10 to 100 nm.
• US 2006/0235254 A1 discloses a process for the isomerization of 1-butene to 2-butene in the presence of a catalyst and hydrogen.
• the aim of this method is to minimize the amount of butane that is produced as possible.
• the catalyst contains palladium, platinum or nickel on alumina and is optionally sulfurized before the reaction.
• EP 0 636 677 B1 discloses a process for isomerizing external olefins to obtain internal olefins. This process is carried out in the presence of a catalyst containing palladium on a support material.
• the catalyst may optionally contain 0.05 to 10% sulfur.
• US 3,531,545 discloses a process for isomerizing olefins to obtain 2-olefins.
• the catalyst used contains a noble metal on alumina.
• the isomerization is optionally carried out in the presence of a sulfur-containing compound.
• a disadvantage of the known processes are too low yields, for example by side reactions such as branching, low selectivity and high prices of the catalysts. Furthermore, in the known methods, insufficient activity, i. H. an insufficient isomerization of the starting compounds to the desired products, and to observe an excessive hydrogenation to saturated compounds. It is an object of the present invention to provide an improved catalyst and an improved process for the isomerization, in particular hydroisomerization, of olefins from olefin-containing hydrocarbon mixtures having 4 to 20 C atoms, in particular linear C 4 to 8 C olefins To provide an improved yield and selectivity with respect to the desired products in conjunction with a reduced formation of undesired by-products, for example saturated compounds.
• a catalyst was found containing alumina as a support material and as an active component palladium or platinum, obtainable by a) impregnation of an alumina support with a solution containing at least one salt of the active component palladium or platinum and b) drying of the catalyst thus obtained, characterized in that c) the catalyst thus obtained over a period of 1 to 24 hours at a temperature of 30 up to 200 ° C treated with hydrogen or a mixture of hydrogen and at least one inert gas, and d) the thus reduced catalyst thereafter stored for a period of 1 hour to 10 days at a temperature of 10 to 100 ° C in the presence of hydrogen.
• the metals to be deposited on the support according to process step a) - palladium or platinum - can be applied to the support by any known method, for example by coating from the gas phase (chemical or physical vapor deposition) or impregnation of the support material with a solution which the deposited Contains substances and / or compounds.
• the preferred method is the impregnation with a solution of the metals to be deposited in the form of their salts or mixtures of their salts, which convert in the course of further catalyst production in the substances to be deposited.
• These metal salts can be deposited individually and / or in partial quantities in several process steps or jointly and completely in one process step.
• the metal salts are, above all, those salts which can easily be converted into the corresponding oxides in the calcination, for example hydroxides, carbonates, chlorides, nitrates, nitrites, acetates and formates. Some of these metal salt solutions are acidic due to the anions used. Neutral solutions are acidified in a preferred embodiment prior to impregnation by, for example, mineral acids.
• the carrier is impregnated with a solution of salts of the components to be separated, the volume of the solution being so dimensioned that the solution is taken up almost completely by the pore volume of the carrier ("in-ipus wetness" method).
• the concentration of the salts in the solution is so dimensioned that after impregnation and conversion of the impregnated support to the finished catalyst, the components to be deposited are present in the desired concentration on the catalyst.
• the salts are chosen so as not to leave any residues which interfere with the preparation of the catalyst or its subsequent use.
• the preparation of the catalyst according to the invention is preferably carried out by single-stage impregnation of the carrier by the incipient wetness method, for example i) with a nitrate solution of the nitrates or ii) with a hydrochloric acid solution of the chlorides of the metals to be deposited, in particular with a hydrochloric acid solution of palladium chloride.
• the concentration of nitric acid used in case i) is at least so high that a clear solution is present.
• the pH of the solution is at most 5, preferably at most 2, and most preferably at most 1.
• the impregnated support is dried in process step b) in a conventional manner, generally at a temperature above 60 ° C, preferably above 80 ° C and most preferably above 100 ° C, for example at a temperature in the range from 120 ° C to 300 ° C.
• the drying is continued until substantially all the water present in the impregnated carrier has escaped, which is generally the case after a few hours. Typical drying times are in the range of one to 30 hours and depend on the set drying temperature, higher temperature shortens the drying time.
• the drying can be further accelerated by applying a negative pressure.
• step c) first a reduction over a period of 1 to 24 hours, preferably 3 to 20 hours, more preferably 6 to 14 hours in a Temperature of 30 to 200 ° C, preferably 50 to 180 ° C, particularly preferably 60 to 130 ° C by treatment with hydrogen or a mixture of hydrogen and at least one inert gas, for example, noble gases such as helium, neon or argon, nitrogen, carbon dioxide and / or lower alkanes, such as methane, ethane, propane and / or butane. Nitrogen is to be mentioned as a preferably used inert gas.
• noble gases such as helium, neon or argon
• nitrogen, carbon dioxide and / or lower alkanes such as methane, ethane, propane and / or butane.
• Nitrogen is to be mentioned as a preferably used inert gas.
• Such inert gases in hydrogen are preferably present in a concentration of less than 30% by volume.
• the catalyst thus reduced is then for a period of 1 hour to 10 days, preferably from 6 hours to 8 days, more preferably from 1 to 7 days, most preferably from 3 to 6 days at a temperature of 10 to 100 ° C, preferably 20 to 80 ° C, more preferably 25 to 60 ° C in the presence of hydrogen or a mixture of hydrogen and at least one of the above-mentioned inert gases.
• a preferred embodiment of the catalyst according to the invention contains alumina as support material and as active component palladium or platinum, obtainable by a) impregnation of an alumina support with a solution containing at least one salt of the active component palladium or platinum and b) drying of the catalyst thus obtained, characterized in that c) the catalyst thus obtained over a period of 1 to 24 hours, preferably 3 to 20 hours, more preferably 6 to 14 hours at a temperature of 30 to 200 ° C, preferably 50 to 180 ° C, particularly preferably 60 to 130 ° C is treated with hydrogen or a mixture of hydrogen and at least one inert gas, preferably nitrogen, and d) the catalyst thus reduced thereafter for a period of 1 hour to 10 days, preferably from 6 hours to 8 days, more preferably from 1 to 7 days , most preferably from 3 to 6 days at a temperature of 10 to 100 ° C, bevo Rzugt 20 to 80 ° C, more preferably 25 to 60 ° C in the presence of hydrogen or a mixture of hydrogen and
• a further preferred embodiment of the catalyst according to the invention is characterized in that the catalyst after process step c) and before process step d) in an additional process step ci) for a further 1 to 16 hours, preferably 2 to 12 hours, more preferably 4 to 10 hours a temperature of 10 to 100 ° C, preferably 20 to 80 ° C in the hydrogen atmosphere, wherein the temperatures of the process steps c), Ci) and d) are each different.
• a further embodiment of the catalyst according to the invention is characterized in that the catalyst is calcined after drying in process step b) and before the hydrogen treatment in process step c).
• This calcination is preferably carried out when using the nitrates of the metals to be deposited and serves essentially to convert the impregnated salts into the components or precursors of such components to be deposited and differs from a later-described calcination, the preparation of the support material and the support structure serves.
• this calcination essentially the nitrates in metals and / or metal oxides remaining in the catalyst and nitrous gases which are released decompose.
• the calcination temperature is generally in the range of 250 ° C to 900 ° C, preferably in the range of 280 ° C to 800 ° C, and more preferably in the range of 300 ° C to 700 ° C.
• the calcination time is generally between 0.5 and 20 hours, more preferably between 0.5 and 10 hours, and most preferably between 0.5 and 5 hours.
• the calcination is carried out in a conventional furnace, for example in a rotary kiln, in a belt calciner or in a chamber furnace. The calcination can be followed directly by the drying without intermediate cooling of the impregnated and dried support.
• a further preferred embodiment of the catalyst according to the invention contains alumina as support material and as active component palladium or platinum, obtainable by a) impregnation of an alumina support with a solution containing at least one salt of the active component palladium or platinum and b) drying of the catalyst thus obtained, characterized in that c) the catalyst thus obtained over a period of 1 to 24 hours, preferably 3 to 20 hours, more preferably 6 to 14 hours at a temperature of 30 to 200 ° C, preferably 50 to 180 ° C, particularly preferably 60 up to 130 ° C with hydrogen or a mixture of hydrogen and at least one inert gas, preferably nitrogen treated, and d) the thus reduced catalyst thereafter for a period of 1 hour to 10 days, preferably from 6 hours to 8 days, more preferably from 1 to 7 days, most preferably from 3 to 6 days at a temperature of 10 to 10 0 ° C, preferably 20 to 80 ° C, particularly preferably 25 to 60 ° C in the presence of hydrogen or a mixture of hydrogen and at
• the treatment of the catalyst according to the invention with atmospheric oxygen can be carried out by customary methods known to the person skilled in the art, for example by mixing the hydrogen or the hydrogen / inert gas mixture in process step d) through a nitrogen / air-oxygen mixture (ratio of nitrogen to air: 5: 1 to 1: 5, preferably 2: 1 to 1: 2, more preferably 1: 1) at temperatures in the range replaced from 20 ° C to 35 ° C and filling the catalyst in the presence of this nitrogen / atmospheric oxygen mixture in containers.
• a nitrogen / air-oxygen mixture ratio of nitrogen to air: 5: 1 to 1: 5, preferably 2: 1 to 1: 2, more preferably 1: 1: 1
• Another way of bringing into contact with atmospheric oxygen can be in the form that the catalyst is first flushed with nitrogen after process step d) and then filled into containers without inerting in the presence of atmospheric oxygen.
• the carrier material may have different shapes.
• the support material in the form of a finely divided powder will usually be used to prepare the catalysts according to the invention.
• the powder preferably has a particle size in the range from 1 to 200 ⁇ m, in particular from 1 to 100 ⁇ m.
• moldings of the support material which are e.g. are obtainable by extrusion, extrusion or tableting and which are e.g. may have the form of spheres, tablets, cylinders, strands, rings or hollow cylinders, stars and the like.
• the dimensions of these moldings usually range from 1 mm to 25 mm.
• catalyst strands with strand diameters of 1.5 to 5 mm and strand lengths of 2 to 25 mm are used.
• the alumina support material is used in the form of spherical moldings.
• the spherical shaped bodies generally have a diameter in the range from 1 to 6 mm, preferably in the range from 2 to 5.5 mm, particularly preferably in the range from 3 to 5 mm.
• the moldings in particular the spherical moldings, advantageously have a (side) compressive strength of> 40 Newton (N), especially of> 50 N, more particularly of> 60 N, more particularly of> 70 N, e.g. in the range of 60 to 90 N up.
• N side compressive strength
• the catalyst tablet was loaded between two parallel plates on the shell side or, for example, the catalyst ball between two parallel plates with increasing force, until fracture occurred.
• the force registered at the break is the (side) compressive strength.
• the determination was made on a testing device from Zwick, Ulm, with a fixed turntable and a freely movable, vertical punch, which pressed the molded article against the fixed turntable.
• the freely movable punch was connected to a pressure cell for receiving the force.
• the device was controlled by a computer, which registered and evaluated the measured values. From a well-mixed catalyst sample 25 perfect (ie free of cracks and possibly without ejected edges) molded bodies were taken, determined their (lateral) compressive strength and then averaged.
• the shaped articles in the form of extrudates advantageously preferably have a cutting hardness of> 30 Newton (N), especially of> 40 N, more particularly of> 50 N, for example in the range of 45 to 70 N.
• N 30 Newton
• the cutting hardnesses were measured on an apparatus from Zwick (type:
• the cutting hardness was determined in detail as follows: extrudates were loaded by a blade of 0.3 mm thickness with increasing force until the extrudate was severed. The force required for this is the cutting hardness in N (Newton). The determination was carried out on a testing device from Zwick, Ulm, with fixed turntable and freely movable, vertical punch with built-in cutting edge of 0.3 mm thickness.
• the moving punch with the cutting edge was connected to a load cell for force absorption and moved during the measurement against the fixed turntable on which the extrudate to be measured lay.
• the tester was controlled by a computer which registered and evaluated the results of the measurements. From a well-mixed catalyst sample 15 straight, crack-free as possible extrudates were taken with a mean length of 2 to 3 times the diameter, the cutting hardness determined and then averaged.
• Electron microscopic investigations have furthermore shown that, in the case of the present inventive catalyst, a shell catalyst is present.
• the concentration of the active component within a catalyst grain decreases from outside to inside, with a palladium or platinum layer on the grain surface.
• crystalline palladium or platinum can be detected in the shell by means of SAD (Selected Area Diffraction) and XRD (X-Ray Diffraction).
• the active component is substantially enriched in a near-surface boundary layer of the carrier.
• more than 80% by weight, preferably more than 90% by weight, and more preferably more than 95% by weight, of the active component in a layer not more than 2000 microns thick is derived from the geometric surface of the Catalyst particle is limited included.
• this layer is not thicker than 1000 microns, more preferably not thicker than 300 microns, most preferably the layer is in the range of 150 to 30 microns.
• the catalyst according to the invention is also characterized in that the active component is highly dispersed.
• the dispersity of the active component in the catalyst is averaged preferably in the range of 20 to 60%, in particular in the range of 30 to 50% (in each case measured by CO sorption according to DI N 66136-3).
• a further particularly preferred embodiment of the catalyst described at the beginning is characterized in that the active component used is palladium in an amount of 0.05 to 2.0% by weight, preferably 0.1 to 1.0% by weight, more preferably 0 , 2 to 0.8 wt .-%, most preferably 0.25 to 0.5 wt .-%, based on the total weight of the catalyst used.
• Another particularly preferred embodiment of the above-described palladium-containing catalyst is characterized in that the alumina support is impregnated with a solution containing palladium chloride and / or palladium hydroxide.
• the alumina support of the catalyst according to the invention is preferably a mixture of ⁇ -, ⁇ - and ⁇ -alumina, more preferably of ⁇ -, ⁇ -, ⁇ - and ⁇ -alumina.
• the carrier may contain, in addition to unavoidable impurities, other additives to some extent.
• other inorganic see oxides such as oxides of IIA., HIB., IVB., INA. and IVA. Group of the Periodic Table of the Elements, in particular silica, titania, zirconia, zinc oxide, magnesium oxide, sodium oxide and calcium oxide.
• the maximum content of the support to such oxides other than alumina depends on the actual oxide present, but to be determined in the individual case on the basis of the X-ray diffraction diagram of the catalyst, since a change in the structure associated with a significant change in the X-ray diffraction pattern.
• the content of such, other than alumina oxides below 50 wt .-%, preferably below 30 wt .-%, more preferably below 10 wt .-%.
• the purity of the alumina is preferably higher than 99%.
• a suitable aluminum-containing raw material preferably gibbsite
• a peptizer such as water, dilute acid or dilute base.
• the acid for example, a mineral acid such as nitric acid or an organic acid such as formic acid is used.
• an inorganic base such as ammonia is preferably used.
• the acid or base is generally dissolved in water.
• the peptizer used is water or dilute aqueous nitric acid.
• the concentration of the nonaqueous fraction in the peptizer is generally 0 to 10% by weight, preferably 0 to 7% by weight, particularly preferably 0 to 5% by weight. The peptization is continued until the mass is well malleable.
• the mass is then converted to the desired carrier form by conventional methods. Pern deformed, for example by extrusion, extrusion, tableting or agglomeration. For deformation, any known method is suitable. If necessary or advantageous conventional additives can be used. Examples of such additives are extruding or tableting aids, such as polyglycols or graphite.
• the carrier raw material prior to deformation additives which influence the pore structure of the carrier after calcination in a known manner as Ausbrennscher, for example polymers, fibers, natural fuels, such as nutshell flours, or other conventional additives.
• the use of boehmite in a particle size distribution and the addition of burnout materials resulting in a pore radius distribution of the finished support is 50-90 vol.% Of the total pore volume in the form of pores having an average diameter in the range of 0.01 to 0.1 ⁇ and 10 to 50 vol .-% of the total pore volume in the form of pores having a mean diameter in the range of 0.1 to 1 ⁇ present.
• the measures necessary for this purpose are known to those skilled in the art.
• the shaped bodies are dried in a customary manner, generally at a temperature above 60 ° C., preferably above 80 ° C., more preferably above 100 ° C., in particular at a temperature in the range from 120 to 300 ° C.
• the drying is continued until water present in moldings has escaped substantially completely from the moldings, which is generally the case after a few hours.
• Typical drying times are in the range of 1 to 30 hours and are dependent on the set drying temperature, with a higher temperature shortens the drying time.
• the drying can be further accelerated by applying a negative pressure.
• the shaped bodies are converted by calcination into a finished carrier.
• the calcination temperature is generally in the range of 900 to 150 ° C, preferably in the range of 1000 to 1 120 ° C, particularly preferably in the range of 1050 to 1 100 ° C.
• the calcination time is generally between 0.5 and 5 hours, preferably between 1 and 4 hours, more preferably between 1, 5 and 3 hours.
• the calcination takes place in a conventional furnace, for example in a rotary kiln, in a tunnel kiln, in a belt calciner or in a chamber kiln.
• the calcination can be followed directly by the drying without intermediate cooling of the moldings.
• the alumina support thus obtained has a specific surface area (BET, Brunauer - Emmet plate, determined in accordance with DIN 66131 by nitrogen adsorption at 77 K) of from 20 to 200 m 2 / g, preferably from 30 to 100 m 2 / g, particularly preferably from 35 up to 90 m 2 / g, up.
• the surface can be varied by known methods, in particular use of finely divided or coarser starting materials, calcination time and calcination temperature. After calcination - as already described above - the active composition and optionally further additives are deposited on the support thus produced.
• the invention also provides a process for the preparation of the above-mentioned catalyst by a) impregnating an aluminum oxide support with a solution comprising at least one salt of the active component palladium or platinum and; b) drying of the catalyst thus obtained; c) treatment of the catalyst after drying with hydrogen or a mixture of hydrogen and at least one inert gas for a period of 1 to 24 hours at a temperature of 30 to 200 ° C; and d) storing the thus reduced catalyst for a period of 1 hour to 10 days at a temperature of 10 to 100 ° C in the presence of hydrogen or a mixture of hydrogen and at least one inert gas, and optionally subsequently contacting the catalyst
• a preferred embodiment of the process according to the invention is characterized in that the catalyst after process step c) and before process step d) in an additional process step ci) for a further 1 to 10 hours at a temperature of 10 to 100 ° C in the hydrogen atmosphere, wherein the temperatures of process steps c), Ci) and d) are each different.
• a further preferred embodiment of the process according to the invention is characterized in that the alumina support in process step a) is impregnated with a solution of one or more salts of palladium.
• a further preferred embodiment of the process according to the invention is characterized in that the catalyst is calcined after drying in process step b) and before the hydrogen treatment in process step c).
• a further preferred embodiment of the process according to the invention is characterized in that the aluminum oxide used in step a) ger by a- ⁇ ) treatment of an aluminum-containing raw material with water, dilute acid or dilute base, 82) deformation to form bodies, 83) drying of the moldings and a 4 ) calcination of the dried moldings.
• a further preferred embodiment of the process according to the invention is characterized in that, in process step a-1, gibbsite is used as the aluminum-containing raw material.
• a further preferred embodiment of the method according to the invention is characterized in that, prior to drying in method step 83), a hydrothermal treatment of the aluminum oxide carrier takes place in the autoclave.
• the present invention also provides a process for activating a catalyst comprising alumina as support material and as active component palladium or platinum, characterized in that c) the catalyst over a period of 1 to 24 hours at a temperature of 30 to 200 ° C with Treated hydrogen or a mixture of hydrogen and at least one inert gas, and d) the thus reduced catalyst thereafter for a period of 1 hour to 10 days at a temperature of 10 to 100 ° C in the presence of hydrogen or a mixture of hydrogen and stored at least one inert gas.
• a preferred embodiment of the process is characterized in that the catalyst is obtainable by a) impregnation of an aluminum oxide support with a solution containing at least one salt of the active component palladium or platinum and b) drying of the catalyst thus obtained.
• a further preferred embodiment of the process is characterized in that the catalyst is subsequently brought into contact with atmospheric oxygen after the hydrogen treatment in process step d).
• process steps a) to d For a more precise interpretation of process steps a) to d), reference is made to the already described process descriptions including the preferred embodiments. Furthermore, the object mentioned was achieved by a process for the isomerization of olefins from olefin-containing hydrocarbon mixtures having 4 to 20 carbon atoms, preferably of linear aliphatic alpha-olefins from olefin-containing hydrocarbon mixtures having 4 to 8 carbon atoms, more preferably one Process for the isomerization of 1-butene to 2-butene at temperatures of 10 to 150 ° C and pressures of 1 to 35 bar in the presence of the above catalyst.
• the isomerization according to the invention can be carried out in any apparatus in which a continuous process is possible.
• the isomerization is preferably carried out in a trickle-bed manner in a tubular reactor which contains the fixed-bed catalyst to be used according to the invention.
• the tube reactor preferably contains a gas distribution in the upper part, for example in the form of a filter plate, a static mixer or a nozzle.
• the gas distribution is used to supply gas mixture, for example hydrogen / nitrogen, wherein the reactor cross-section is preferably gassed evenly.
• the compound to be isomerized is first passed through a heating zone, mixed with the gas and passed into the reactor.
• the catalyst loading is adjusted so that at the reactor output a conversion of the olefin of preferably 30 to 100%, more preferably 50 to 100%, most preferably 50 to 90%, is achieved.
• the process according to the invention is preferably carried out in the presence of hydrogen.
• the hydrogen gassing is adjusted as a function of temperature and total pressure so that a hydrogen partial pressure of 0.1 to 25 bar, preferably 5 to 20 bar, in particular 5 to 12 bar is maintained.
• the passed-through hydrogen can be run in the reactor discharge after condensation of low boilers as exhaust gas or recycled back into the process.
• the process according to the invention is carried out in the presence of an inert gas, for example nitrogen or methane.
• the isomerization is preferably carried out at a pressure of 1 to 35 bar absolute, in particular 5 to 25 bar absolute.
• the isomerization is generally carried out at temperatures between 10 and 150 ° C, preferably 30 to 120 ° C, for example 50 to 100 ° C.
• catalyst loadings of 0.5 to 15 kg / (1 catalyst X h), 1 to 10 kg / l of catalyst x h are carried out.
• the isomerization is carried out in the presence of hydrogen.
• the present invention therefore preferably relates to the process according to the invention, wherein it is carried out in the presence of hydrogen.
• the isomerization is carried out in the presence of a mixture of hydrogen and inert gas, preferably methane or nitrogen, wherein the hydrogen used in a relative volume fraction of 80 to 98 mol% based on the total amount of hydrogen and methane or nitrogen used becomes.
• a mixture of hydrogen and inert gas preferably methane or nitrogen
• Hydroisomerization i. the process according to the invention in the presence of hydrogen may be accompanied by hydrogenation.
• This embodiment is preferred, for example, when the reaction mixture also contains acetylenes, for example butyne and / or vinyl acetylene, or dienes, for example butadiene, so that these are hydrogenated in the presence of the isomerization catalyst.
• the process according to the invention is preferably carried out together with a selective hydrogenation of acetylenes or diolefins.
• acetylenes for example butyne and / or vinylacetylene and / or butadiene
• the olefins to be isomerized according to the invention can be present as uniform compounds or as a mixture of alpha-olefins with different chain lengths of 4 to 20 C atoms, preferably 4 to 8 C atoms.
• linear alpha-olefins used according to the invention as substrates are 1-n-butene, 1-n-pentene, 1-n-hexene, 1-n-heptene or 1-n-octene.
• the linear alpha-olefins having 4 to 8 carbon atoms used in accordance with the invention can be used as individual compounds or as a mixture of several of the compounds mentioned. If appropriate, further organic compounds may be present in the reaction mixture, for example olefins having two or more double bonds and 4 to 8 C atoms, for example butadiene.
• the corresponding 2-olefins are preferably formed from the 1- olefins used, ie. H. in the isomerization according to the invention, the double bond preferably shifts from the 1-position to the 2-position.
• the 2-olefins preferably formed according to the invention can be obtained as cis and / or trans isomers, depending on their chain length.
• 1-butene is isomerized to cis- and / or trans-2-butene by the process according to the invention, wherein the ratio of 2-butene to 1-butene in the exit of the isomerization stage is between 3 and 30, preferably between 4 and 25, while the ratio of 2-butene to 1-butene in the input stream to the isomerization between
• inventively isomerized olefins preferably linear 2-olefins
• the internal olefins are furthermore required, for example, for the preparation of gasolines via alkylation or for reactions with other reagents in electrophilic additions such as halogenation, water addition or dimerization, oligomerization and polymerization, for example radical reactions of the internal olefins.
• the catalyst was treated with hydrogen at 120 ° C. for 12 hours.
• Spherical shaped bodies of alpha / theta / kappa-Al 2 O 3 with a diameter of 3 mm and a BET specific surface area of 40 m 2 / g were followed by a hydrochloric acid PdC solution, which was neutralized shortly before impregnation with a NaHCO 3 solution soaked in the incipient wetness method. Subsequently, the impregnated support was washed and dried at 150 ° C for 12 hours. The palladium content of the finished catalyst was 0.25% by weight.
• the catalyst was treated for 12 hours at 120 ° C with hydrogen.
• Spherical shaped bodies of alpha / theta / kappa-A Os with a diameter of 3 mm and a BET specific surface area of 40 m 2 / g were neutralized with a PdC hydrochloric acid solution which was neutralized with a NaHCO 3 solution shortly before impregnation soaked in incipient wetness method. Subsequently, the impregnated support was washed and dried at 150 ° C for 12 hours. The palladium content of the finished catalyst was 0.3% by weight.
• the catalyst was treated for 12 hours at 120 ° C with hydrogen.
• Catalyst E (according to the invention) Spherical shaped bodies of alpha / theta / kappa-Al 2 O 3 with a diameter of 3 mm and a BET specific surface area of 40 m 2 / g were treated with a PdC hydrochloric acid solution shortly before impregnation was neutralized with a NaHCO 3 solution soaked in the incipient wetness method. Subsequently, the impregnated support was washed and dried at 150 ° C for 12 hours. The palladium content of the finished catalyst was 0.25% by weight.
• the catalyst was first treated for 12 hours at 120 ° C with hydrogen, then stored for 8 hours at 60 ° C and last for another 6 days at 30 ° C under a hydrogen atmosphere.
• Catalyst F (according to the invention) Spherical shaped bodies of alpha / theta / kappa-Al 2 O 3 with a diameter of 3 mm and a BET specific surface area of 40 m 2 / g were treated with a PdC hydrochloric acid solution shortly before impregnation neutralized with a NaHCO 3 solution was impregnated by the incipient wetness method. Subsequently, the impregnated support was washed and dried at 150 ° C for 12 hours. The palladium content of the finished catalyst was 0.3% by weight.
• Spherical shaped bodies of alpha / theta / kappa-A Os with a diameter of 3 mm and a BET specific surface area of 40 m 2 / g were neutralized with a PdC hydrochloric acid solution which was neutralized with a NaHCO 3 solution shortly before impregnation soaked in incipient wetness method. Subsequently, the impregnated support was washed and dried at 150 ° C for 12 hours. The palladium content of the finished catalyst was 0.3% by weight.
• the catalyst was first treated for 12 hours at 120 ° C with hydrogen, then stored for 8 hours at 60 ° C and last for another 6 days at 30 ° C under a hydrogen atmosphere.
• the catalyst was purged with nitrogen at 30 ° C and then treated for 2 hours with an air-nitrogen mixture, wherein the proportion of the air flow was gradually increased within 1 hour and last 50%.
• the experiments for isomerization of 1-butene to 2-butene were carried out in a fixed bed reactor with circulation and separator in the presence of one of the catalysts listed in the table.
• a substrate stream (feed) was a raffinate I with 0.5-0.6 vol% butadiene (BD) and a ratio of 2-butene to 1-butene of 0.6 used to 0.7.
• the substrate stream (feed) used was a raffinate II without butadiene with a ratio of 2-butene to 1-butene of 0.8.
• composition of the product obtained was evaluated in terms of the ratio of 2-butene to 1-butene, the formation of 2-butene and n-butane (n-Bu) and the 1-butene isomerization.

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• 2016
  • 2016-07-08 JP JP2018501999A patent/JP2018521848A/ja not_active Withdrawn
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