Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C7/00—Purification; Separation; Use of additives
  • C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
  • C07C7/163—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation
• • 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
  • B01J23/48—Silver or gold
• • 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
  • B01J23/48—Silver or gold
  • B01J23/50—Silver
• • 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
  • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
  • B01J23/66—Silver or gold
• • 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
  • B01J35/19—Catalysts containing parts with different compositions
• • 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
  • B01J37/0009—Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
• • 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
• • 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
  • C07C5/02—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C7/00—Purification; Separation; Use of additives
  • C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
  • C07C7/163—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation
  • C07C7/167—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation for removal of compounds containing a triple carbon-to-carbon bond
• • 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
  • C07C2521/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
  • C07C2521/08—Silica
• • 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
• • 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
  • C07C2523/48—Silver or gold
  • C07C2523/50—Silver

Definitions

• the present invention relates to the field of catalysis. More specifically, the present invention relates to a new hydrogenation catalyst which makes it possible to selectively hydrogenate more unsaturated hydrocarbons such as acetylenes and dienes in olefin mixtures which have been obtained by the cracking process. The present invention further relates to a process for the preparation of such a catalyst and a process for the selective hydrogenation of alkynes and dienes in olefin mixtures with the aid of such a catalyst.
• Olefins are generally produced industrially in so-called cracking processes, for example steam cracking or catalytic cracking by FCC.
• Certain petroleum distillates are heated to temperatures around 900 ° C at which olefins are formed from the alkanes present.
• the crude mixture obtained is then separated by distillation, the fractions being cut so that the C2 to C5 + olefins are separated from one another.
• the olefins obtained are then used in further processing.
• alkynes (acetylenes) and dienes also form, the proportion of which depends on the process and the experimental conditions chosen. However, these alkynes and dienes often interfere with further processing and storage.
• the so-called C2 cut which contains ethylene
• Large quantities of ethylene are catalytically processed into polyethylene.
• ethylene used for such a polymerization may only have an acetylene content of less than about 1 ppm.
• C3- Electricity that contains propane (Allen) and propyne in addition to propene.
• propane (Allen) and propyne Large amounts of propene are also catalytically processed into polypropene in a process similar to that of ethylene.
• a propene which can be used for the polymerization may in general only contain an amount of allene and propyne which is below about 10 ppm.
• the other cuts in the cracking process also produce products that are undesirable for the purposes of further processing.
• vinyl acetylene is hydrogenated as an impurity before the butadiene extraction.
• butadiene can be specifically converted into butene, so that such a refinement of the C4 stream is desired.
• the so-called C5 + section contains cyclic pentenes and pentadiene, which should be converted into non-interfering products while retaining the linear C5 building blocks and the unsaturated C5 + components.
• One method for removing the by-products mentioned is the selective hydrogenation of these alkynes and dienes.
• the impurities are converted into non-interfering components or preferably into the valuable product of the hydrocarbon fraction.
• the main problem with such a process is that on the one hand the catalyst that is used must have sufficient activity to completely hydrogenate the by-products, which are only present in relatively small amounts compared to the olefin, and thus the content of impurities to press values that are tolerable during further processing. If one realizes that an impurity content of less than 1 ppm must sometimes be reached, as is the case with polyethylene, it becomes clear that the catalyst used in the selective hydrogenation must have a high activity.
• Such a catalyst must also have a very high selectivity or, in other words, a low specific activity with respect to the olefin to be processed, so that it is not hydrogenated to the corresponding alkane or is only hydrogenated to a very small extent and is no longer available.
• the catalysts used in the selective hydrogenations should also have the property of not catalyzing the oligomerization of alkynes and dienes. This reaction causes the formation of oily residues that accumulate on the catalyst. The result is a deactivation of the catalyst which, depending on the amount of by-products formed, can occur after less than a month.
• selectively hydrogenation generally uses supported catalysts of metals which are generally used in hydrogenations, mainly heterogeneous catalysts of the tenth group of the periodic table, ie Ni, Pd and Pt. Pd is used in most cases.
• the carrier used is generally a porous inorganic oxide, for example silica, aluminosilicate, titanium dioxide, zirconium dioxide, zinc aluminate, zinc titanate, spinels and / or mixtures of such carriers, but usually aluminum oxide or silicon dioxide is used. Promoters or other additives may also be present.
• Process for the selective hydrogenation of unsaturated compounds in hydrocarbon streams which contain them both as liquid phase hydrogenation or mixed gas / liquid phase hydrogenation, in trickle or bottoms mode, and also as pure gas phase hydrogenation.
• the catalysts mentioned are modified. It is generally known that the desired increases in selectivity for the metals mentioned above can often be achieved by adding CO during the hydrogenation. However, this requires special safety measures due to the toxicity of the CO. In addition, a product containing CO is obtained in this way, which must first be cleaned again for some further uses.
• EP-A-0 064 301 describes a catalyst for the selective hydrogenation of acetylene, which consists of Pd which has been modified with Ag, and ⁇ -alumina is used as the support.
• the Pd content is from 0.01 to 0.025% by weight, Ag is present in 2 to 10 times the amount of Pd.
• the silver is distributed over all catalyst particles, while 90% of the palladium is in an edge zone of 300 ⁇ m.
• the two applications EP-A-0 686 615 and EP-A-0 780 155 describe a catalyst for selective hydrogenation in the gas phase of alkynes in a C2 or C3 stream.
• the catalyst is palladium, to which a Group 11 metal has been added.
• Aluminum oxide is used as the carrier material.
• At least 80% of both metals are present in a zone that extends from the edge of the catalyst particle to a radius that is 80% of the outer radius of the catalyst particle.
• the palladium content is 0.01 to 0.5% by weight of the catalyst and the ratio of the Group 11 metal to the palladium is 0.05 to 0.4 (686 615) and 0.4 to 3 (780, respectively) 155).
• the preferred Group 11 metal is silver in both applications.
• the hydrogenation-active metal is platinum and / or palladium, which is doped with copper and / or silver.
• DE-A-2 156 544 discloses a process for the production of ethylene by selective catalytic gas-phase hydrogenation of acetylene in the C2- Section of the olefin representation using a palladium catalyst mounted on a silica support.
• the catalyst is modified by zinc.
• EP-A-0 764 463 describes a selective hydrogenation catalyst which has palladium which has been modified with a promoter metal from groups 1 and 2 of the periodic table.
• the catalyst is attached to a carrier based on silicon dioxide.
• DE-P-31 19 850 describes a process which describes the selective hydrogenation of butadiene in a butene-1-containing C4 fraction.
• the catalyst used is applied to aluminum oxide or silicon dioxide with a specific surface area of 10 to 200 m 2 / g, and the catalyst consists of a mixture of palladium and silver or compounds of these metals.
• the palladium content is 0.05 to 5% by weight, the silver content 0.05 to 1% by weight.
• the catalyst described in this reference is only suitable for the selective hydrogenation of butadiene in C4 streams.
• Catalyst is present in pores with a diameter above 100 nanometers.
• the catalyst is used to remove alkynes, dienes and / or monounsaturated hydrocarbons from material flows. It can be said that until now it has not been possible to develop a selective hydrogenation catalyst for alkynes and dienes which is mounted on a support other than aluminum oxide, for example silicon dioxide, and has the same performance as catalysts mounted on aluminum oxide as a support material.
• the object of the present invention is therefore to provide a catalyst for the selective hydrogenation of alkynes and dienes in C2-C5 + olefin mixtures, which is mounted on a support other than aluminum oxide, but the catalyst should have the same performance as those in which Alumina was used as a carrier. Furthermore, such a catalyst should be as simple to manufacture as possible. The catalyst should preferably also be lighter than those in which aluminum oxide was used as the support material.
• This object is achieved by a catalyst for the selective hydrogenation of alkynes and dienes in C2-C5 + olefin mixtures, the catalyst containing
• metals are applied to a support selected from the group consisting of silicon dioxide, titanium dioxide, zirconium oxides, spinels, zinc aluminate, zinc titanate or mixtures thereof, and wherein the metal of the eleventh group is homogeneously distributed over the cross section of the catalyst core and the metal the tenth group is concentrated in a near-surface boundary layer of the catalyst core.
• This object is further achieved by a method for producing such a catalyst, which method is characterized in that first the metal of the eleventh group is applied homogeneously on the support and then the metal of the tenth group is applied.
• the metal of the eleventh group is preferably incorporated prior to the deformation of the carrier, and the metal of the tenth group is preferably applied by impregnation with a solution of a salt of the respective metal.
• Such a catalyst can advantageously be used in the selective hydrogenation of alkynes and dienes in C2-C5 + olefin mixtures.
• olefin mixtures in connection with the present invention are preferably understood to be so-called hydrocarbon streams, that is to say the products obtained in the cracking of petroleum distillates or natural gas, which largely contain olefins.
• the process according to the invention can also be used for the selective hydrogenation of alkynes and dienes in olefin mixtures which have been obtained in other processes known to a person skilled in the art.
• silicon dioxide is particularly suitable as the carrier material.
• Silicon dioxide has the advantage that it is specifically much lighter than aluminum oxide.
• Supported catalysts with a low bulk density are generally cheaper than catalysts with a high bulk density.
• other support materials are suitable for being used in a hydrogenation catalyst according to the invention. These are, for example, titanium dioxide, zirconium oxides, zinc aluminate, zinc titanate, or mixtures of the materials mentioned.
• the carrier materials used in the present invention have a BET surface area of 20 to 400 m 2 / g, preferably 100 to 160 m 2 / g, and a pore volume of 0.1 to 1.5 ml / g, preferably 0.7 to 1.2 ml / g.
• the metal of the tenth group is present in the catalyst according to the invention in amounts of 0.005 to 1% by weight, preferably 0.02 to 0.6% by weight, based on the total mass. It has been found that among the metals in this group, i.e. Nickel, palladium, platinum, the best results can be achieved with palladium. The use of palladium is therefore preferred.
• the metal of the tenth group is essentially enriched in a surface layer of the support near the surface.
• more than 80% by weight, preferably more than 90% by weight, and more preferably more than 95% by weight of the metal or metals in a layer of not more than 0.6 mm in thickness is limited by the geometric surface of the catalyst particle. This layer is preferably not thicker than 0.45 mm.
• An important element of the catalyst according to the present invention is the promoter metal, which is a metal from the eleventh group of the periodic table, ie copper, silver or gold. The addition of this metal and its specific arrangement in the hydrogenation catalyst according to the present invention allow the selective hydrogenation of alkynes and dienes with high activity and selectivity. At the same time, the tendency to form oligomers and thus the resulting catalyst deactivation is reduced.
• the metal of the eleventh group is present in the catalyst according to the invention in amounts of 0.005 to 1% by weight, preferably 0.05 to 0.6% by weight, based on the total mass.
• the ratio of metal of the eleventh group to metal of the tenth group is in the range from 0.01 to 100 in relation to the metal of the tenth group. This ratio is preferably in a range from 0.5 to 30, most preferably 1.5 to 20, in which the best results have been achieved. It is further preferred if the eleventh grade metal is silver.
• the catalyst according to the present invention can be constructed in such a way that only one metal of the eleventh group and one metal of the tenth group or compounds of these metals are present. However, two or more metals of the eleventh group and the tenth group or their compounds can also be present independently of one another in the catalyst.
• the catalyst according to the present invention contains palladium and silver.
• the metal of the eleventh group is distributed over the entire cross section of the catalyst core in the catalyst according to the invention.
• the metal of the eleventh group is applied in one step, before the metal of the tenth group is applied.
• This metal of the tenth group can also be fixed on the carrier with the usual measures known to a person skilled in the art. Again, however, it is preferred if this application is carried out by impregnation with a solution of a suitable salt of the respective metal. This is preferably carried out in such a way that the solution is almost completely absorbed by the pore volume of the carrier ("incipient wetness" method).
• the absorption capacity of the carrier for the impregnation solution does not have to be fully exhausted, so the impregnation solution can be used in an amount of less than 100%, for example not more than 95% by volume, not more than 90% by volume or not more than 85% by volume of the volume of liquid which can be absorbed by the carrier to be soaked
• concentration of the salts in the solution becomes dimensioned such that after impregnation and conversion of the impregnated support to the finished catalyst, the components to be deposited are present on the catalyst in the desired concentration, and the salts are chosen so that they do not leave any residues which interfere with the catalyst preparation or its later use Ammonium salts used.
• the catalysts according to the invention can also contain further promoter metals which are selected from the first and second groups of the periodic table. Sodium, potassium, calcium or barium are preferably used.
• the application is carried out by suitable methods known to a person skilled in the art, for example by impregnation, in parallel with the application of the metal of the tenth and the eleventh group and regardless of the chosen order of application.
• the crude catalysts obtained are dried and calcined at the customary temperatures, this in a single step or two separate steps can be performed. Drying takes place at temperatures from 50 ° C to 250 ° C, preferably 70 ° C to 100 ° C.
• the calcining is carried out at temperatures of 250 ° C. to 700 ° C., preferably 300 ° C. to 650 ° C., it being possible, for example, to use rotary tubes, belt calciners or muffle furnaces.
• the bodies have the usual shape, such as strands, spheres, rings, tablets, and are represented by, for example, tabletting or extinguishing the carriers.
• the catalysts of the invention are suitable for the selective hydrogenation of generally all alkynes and dienes having a carbon number from C2 to C5 in mixtures of these with olefins, generally in hydrocarbon streams obtained during cracking.
• the hydrogenation can take place in the gas phase and in the liquid phase, analogously to known, heterogeneous catalytic hydrogenation processes.
• the hydrogenation can be carried out as a pure gas phase process or as a gas / liquid phase process. These methods are known to a person skilled in the art.
• the reaction parameters for example hydrocarbon throughput, temperature and pressure, are selected analogously to those of known processes.
• the amount of hydrogen used is 0.8 to 5 times, preferably 0.95 to 2 times the amount stoichiometrically necessary for complete conversion.
• Process A denotes) selective hydrogenation of propyne and / or propadiene in C3 streams to propylene
• Process B selective hydrogenation of 1-butyne, 2-butyne, 1,2-butadiene and / or vinyl acetylene in C4 streams to 1,3-butadiene, 1-butene, ice and / or trans-2- butene
• Process C selective hydrogenation of 1-butyne, 2-butyne, 1,2-butadiene, 1,3-butadiene and / or
• Process A is usually used as a single-stage or multi-stage gas phase process with a space velocity of the gaseous C2 stream of 500 m 3 / m 3 * h, based on the catalyst volume, up to 10,000 m 3 / m 3 * h at a temperature of 0 ° C up to 250 ° C and a pressure of 0.01 bar to 50 bar.
• Process B is usually carried out as a single-stage or multi-stage gas phase process with a space velocity of the gaseous C3 stream of 500 m 3 / m 3 * h, based on the catalyst volume, up to 10,000 m / m * h or gas / liquid phase process a space velocity of the liquid C3 flow of 1 m 3 / m 3 * h, based on the K Kaattaallyyssaattoorrvvoolluummeenn , bbiiss 5500 mm // mm ** hh bbeeii eeiinneerr 1 temperature from 0 ° C to 180 ° C and a pressure of 0 , 01 bar to 50 bar.
• Process C is usually used as a gas / liquid phase process with a space velocity of the liquid C4 stream of 1 m 3 / m 3 * h, based on the catalyst volume, up to 50 m / m * h at a temperature of 0 ° C. to 180 ° C. and a pressure of 2 bar to 50 bar.
• Process C can be used, for example, as a selective so-called “front end vinyl acetylene hydrogenation” before a butadiene extraction.
• Process D is usually used as a one- or two-stage gas / liquid phase process with a space velocity of the liquid C4 stream in the range from 0.1 m 3 / m 3 * h, based on the catalyst volume, to 60 m / m * h, preferably from 1 m / m * h to 50 m 3 / m 3 * h, at a reactor inlet temperature in the range from 20 ° C to 90 ° C, preferably from 20 ° C to 70 ° C, and a pressure in the range from 5 bar up to 50 bar, preferably from 10 bar to 30 bar.
• the process is carried out in two stages, the butadiene content, which in typical C4 streams from steam crackers is in the range from 20% by weight to 80% by weight, based on the total stream, in the first stage to a content in Range from 0.1 wt .-% to 20 wt .-% and in the second stage to the desired residual content in the range of a few ppm by weight down to about 1 wt .-%. It is also possible to distribute the entire reaction over more than two reactors, for example three or four.
• the individual reaction stages can be operated with partial recycling of the hydrocarbon stream, the reflux ratio is usually in the range from 0 to 30.
• Process D can be used, for example, as butadiene hydrogenation in the C4 stream (if butadiene is not considered Product of value is to be obtained) or used as a selective so-called "tail end vinyl acetylene hydrogenation" after the butadiene extraction from the C4 stream.
• Process E is preferably used as a gas / liquid phase process with a space velocity of the liquid C5 + stream of 0.5 m 3 / m 3 * h, based on the catalyst volume, up to 30 m 3 / m 3 * h at a temperature of 0 ° C up to 180 ° C and a pressure of 2 bar to 50 bar.
• Process E can be used, for example, as selective pyrolysis gasoline hydrogenation, as selective hydrogenation of olefins in reformate streams or coke oven condensates, for the hydrogenation of styrene to ethylbenzene.
• the support in the catalysts according to the invention is preconditioned in such a way that the formation of oligomers during the hydration is significantly reduced, in contrast to other hydrogenation catalysts applied to the same supports.
• the service life of the contact increases significantly.
• the often still required addition of CO as a selectivity control agent is no longer necessary.
• the hydrogenation-active metal of the tenth group can itself be provided with high excesses of promoter metal of the eleventh group, without a loss of activity being observed during hydrogenation.
• a catalyst according to the invention was produced by producing a silica support (4 mm extrudates, BET surface area between 120 and 140 m 2 / g, pore volume between 0.8 and 0.95 ml / g) in such a way that during of the pan step, silver in the form of silver nitrate with 0.05% by weight, based on the amount of SiO used, was added to the pan mass. After extrusion into 4 mm strands, the carrier was calcined and then impregnated with 0.025% by weight of palladium in the form of palladium nitrate, based on the carrier mass used, at room temperature. The solution volume used was 90% of the water absorption of the carrier. The contact was dried at 80 ° C and then calcined at 500 ° C.
• Example 2 Catalyst B According to the Invention
• a catalyst according to the invention was produced by producing a silica support (4 mm extrudates, BET surface area between 120 and 140 m 2 / g, pore volume between 0.8 and 0.95 ml / g) in such a way that during of the pan step, silver in the form of silver nitrate with 0.2% by weight, based on the amount of SiO 2 used , was added to the pan mass.
• the support was calcined and then impregnated with 0.06% by weight of palladium in the form of palladium nitrate, based on the support mass used, at room temperature.
• the solution volume used was 90% of the water absorption of the carrier.
• the contact was dried at 80 ° C and then calcined at 500 ° C.
• a comparative catalyst was produced by an aluminum oxide support in the form of a strand with a BET surface area of 8 m Ig with a nitric acid, aqueous solution of 0.045% by weight of silver in the form of silver nitrate based on the support composition used and of 0.025 based on the support composition used %
• aqueous solution of 0.045% by weight of silver in the form of silver nitrate based on the support composition used and of 0.025 based on the support composition used %
• the solution volume used was 90% of the water absorption of the carrier.
• the contact was dried at 80 ° C and then calcined at 400 ° C.
• Example 3 Another comparative catalyst was produced in accordance with Example 8 of application DE 2156544, a catalyst containing 0.025% palladium and 0.01% zinc being obtained on a silica gel support in the form of a 4 mm strand textured product.
• Example 3 Another comparative catalyst was produced in accordance with Example 8 of application DE 2156544, a catalyst containing 0.025% palladium and 0.01% zinc being obtained on a silica gel support in the form of a 4 mm strand textured product.
• Example 3 Another comparative catalyst was produced in accordance with Example 8 of application DE 2156544, a catalyst containing 0.025% palladium and 0.01% zinc being obtained on a silica gel support in the form of a 4 mm strand textured product.
• Catalysts A to D were tested in the selective hydrogenation of acetylene in a C2 stream containing about 1% alkyne at 20 bar and a load of 3000 l / h and an 80% H excess based on the stoichiometric amount.
• the respective activity, measured by the reaction temperature, stability, measured by the deactivation rate of the conversion, and selectivity, measured by the tendency to form oligomers, were tested and compared. Table 1 shows the test results of contacts A to D.
• a silver-doped SiO 2 carrier in the form of 4 mm extreme data was produced by precipitating silica at pH 6 from an ammoniacal sodium-water glass solution by adding sulfuric acid, which filtered off from the aqueous phase, and conductivity by washing with water freed and sprayed into powder (vibrating weight between 350 and 450 g / 1, water content: approx. 25%).
• the spray powder obtained was kneaded with water and with the addition of a defined amount of silver, based on the solid mass used, in the form of an aqueous silver nitrate solution to form an extrudable mass (so-called pan).
• the rolled mass was formed into strands to obtain 4 mm extrudates.
• the strands were dried at 120 ° C and calcined at a defined temperature.
• a product was obtained with a BET surface area of 110 • to 160 m 2 / g and a vibrating weight between 440 and 480 g / 1. The exact surface values and vibrating weights are given in Table 1.
• This carrier material was then impregnated with a defined amount of palladium, based on the carrier mass used, in the form of an aqueous palladium nitrate solution at room temperature. 95% of the water absorption of the carrier was used as the solution volume.
• the material obtained was agitated at a defined temperature with the addition of air and then calcined with agitation at a defined temperature for 1 hour. The exact manufacturing parameters are shown in Table 1.
• the catalysts E to U were tested at 1 bar in a single pass.
• the stream was composed of 1% by volume of acetylene in ethylene and was mixed with 1.8 equivalents of H 2, based on the amount of CH 2 used .
• the temperatures required for a 90% conversion of acetylene and the selectivity values obtained are shown in Table 2.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Materials Engineering (AREA)
• General Chemical & Material Sciences (AREA)
• Analytical Chemistry (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Water Supply & Treatment (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Catalysts (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Priority Applications (8)

Applications Claiming Priority (2)

Related Child Applications (2)

Publications (1)

Family

ID=7931787

Family Applications (1)

Country Status (14)

Cited By (8)

Families Citing this family (23)

Citations (5)

Family Cites Families (13)

• 1999
  • 1999-12-08 DE DE19959064A patent/DE19959064A1/de not_active Withdrawn
• 2000
  • 2000-12-06 CN CNB008168849A patent/CN1178743C/zh not_active Expired - Fee Related
  • 2000-12-06 DE DE50013242T patent/DE50013242D1/de not_active Expired - Lifetime
  • 2000-12-06 JP JP2001543258A patent/JP2003516225A/ja not_active Withdrawn
  • 2000-12-06 US US10/148,798 patent/US7256153B2/en not_active Expired - Fee Related
  • 2000-12-06 AU AU30067/01A patent/AU3006701A/en not_active Abandoned
  • 2000-12-06 CA CA002393984A patent/CA2393984C/en not_active Expired - Fee Related
  • 2000-12-06 KR KR1020027007261A patent/KR100693968B1/ko not_active Expired - Fee Related
  • 2000-12-06 BR BR0016240-0A patent/BR0016240A/pt not_active Application Discontinuation
  • 2000-12-06 ES ES00990659T patent/ES2269224T3/es not_active Expired - Lifetime
  • 2000-12-06 EP EP00990659A patent/EP1242181B1/de not_active Expired - Lifetime
  • 2000-12-06 RU RU2002118603/04A patent/RU2290258C2/ru not_active IP Right Cessation
  • 2000-12-06 WO PCT/EP2000/012283 patent/WO2001041922A1/de not_active Ceased
  • 2000-12-06 AT AT00990659T patent/ATE333935T1/de not_active IP Right Cessation
  • 2000-12-07 TW TW089126088A patent/TWI243709B/zh active
• 2007
  • 2007-02-01 US US11/670,339 patent/US7582805B2/en not_active Expired - Fee Related

Patent Citations (5)

Also Published As

Similar Documents

Legal Events