Abstract:
A catalyst containing a pentasil-type alumosilicates and a binder, in the form of spheres having an average diameter between 0.3 and 7 mm, wherein the BET surface area of the catalyst ranges from 300 to 600 m2/g. Also disclosed is a method for producing the catalyst, wherein primary crystallites of the aluminosilicate having an average diameter of at least 0.01 μm and less than 0.1 μm are mixed with the binder, shaped into spheres having an average diameter between 0.3 and 7 mm, and subsequently calcined. Also disclosed is the use of the catalyst for converting methanol into olefins, in particular propylene. Also disclosed is a method for producing olefins from methanol, in which a feed gas is fed across the catalyst.
Abstract:
With a method configured to generate process gas that contains hydrogen sulfide and sulfur dioxide for the Claus process, hydrogen-sulfide containing feed gas is burnt with pure oxygen by means of several burners opening out into a combustion chamber wherein the pure oxygen is fed into the combustion chamber through a central tube each, the feed gas through a tube arranged coaxially around the central tube and inert gas as purge gas via an annular duct coaxially surrounding the feed gas tube. A favorable option of the method consists in the use of CO2 re-claimed by desorption of laden methanol as purge gas.
Abstract:
For producing methanol from a synthesis gas containing hydrogen and carbon oxides the synthesis gas is passed through a first, water-cooled reactor in which a part of the carbon oxides is catalytically converted to methanol. The resulting mixture containing synthesis gas and methanol vapor is supplied to a second, gas-cooled reactor in which a further part of the carbon oxides is converted to methanol. Subsequently, methanol is separated from the synthesis gas, and synthesis gas is recirculated to the first reactor. The cooling gas flows through the second reactor cocurrent to the mixture withdrawn from the first reactor.
Abstract:
In the production of methanol from a synthesis gas containing hydrogen and carbon oxides, the synthesis gas is passed through a first, preferably water-cooled reactor, in which a part of the carbon oxides is catalytically converted to methanol. The obtained mixture containing synthesis gas and methanol vapor is supplied to a second, preferably gas-cooled reactor, in which a further part of the carbon oxides is converted to methanol. Subsequently, methanol is separated from the synthesis gas, and the synthesis gas is recirculated to the first reactor. To achieve a maximum methanol yield even with an aged catalyst, a partial stream of the synthesis gas is guided past the first reactor and introduced directly into the second reactor.
Abstract:
The invention relates to a reactor for the production of C2 to C8 olefins from gaseous oxygenate and H2O and one or more material flows containing C2 C4, C5, C6, C7, C8 olefin and paraffin at 400° to 470° C., wherein several reaction stages which the material flow can pass through from the top to the bottom, each consisting of a support base with a catalyst layer situated on it, are arranged in a closed, upright container. In order to be able in each case to lower the temperature of the reaction mixture leaving the reaction stages before it enters into the next reaction stage, it is provided that each support base consists of cells which are placed closely next to each other with no gaps and which are securely attached to each other and filled with catalyst, and in the space formed by two neighboring reaction stages, respectively, an assembly of nozzle tubes is installed for spraying a liquid phase containing H2O and DME and/or MeOH, using a water-saturated gas phase containing mainly DME and/or MeOH, in the direction of the following reaction stage downstream.
Abstract:
In the production of purified methanol and/or dimethyl ether from crude methanol, the crude methanol is processed in at least one prepurification stage, a first partial stream of the prepurified methanol is supplied to a final methanol purification and a second partial stream of the prepurified methanol is supplied to a reactor and at least partly converted to dimethyl ether. The dimethyl ether recovered is purified in at least one purification stage, wherein non-reacted methanol is withdrawn from the dimethyl ether purification stage and at least partly supplied to the final methanol purification. In this way, both purified methanol and dimethyl ether can be produced in parallel, wherein the quantities of both products obtained are flexibly adjustable.
Abstract:
A method of removing contaminants from a gas stream utilizing a supersonic venturi including a converging section, a throat, and a diverging section is provided. A contaminated gas stream and a scrubbing liquid stream are introduced into the converging section, thereby forming a mixed stream which experiences choked flow upon exiting. The choked mixed stream is introduced into the throat section wherein the scrubbing liquid is contacted with the contaminated gas stream. The contaminated scrubbing liquid stream is removed from the supersonic venture scrubber, and an essentially pure gas stream is removed from the diverging section. A flow modification device may be introduced into the throat section. The flow modification device may be either axially or radially adjustable in order to effect the atomization of the scrubbing liquid and/or the contacting of atomized scrubbing liquid with the contaminated gas stream within the throat section.
Abstract:
A gas scrubber, equipped with heat exchanger surfaces constructed of thermoplates, suitable for cooling and cleaning a hot gas by avoiding an excessive thermal load of the washing liquid.
Abstract:
Process for producing synthetic natural gas (SNG) which is provided in an energy-efficient way at the inlet pressure into a downstream pipeline system. For this purpose, a synthesis gas containing carbon oxides and hydrogen is converted into a product gas rich in methane by multi-stage catalytic methanation in a main reaction zone and a post-reaction zone, wherein the adjustment of the target pressure is effected by compression before the main reaction zone and/or before or in the post-reaction zone.
Abstract:
For producing synthesis gas by autothermal reformation of gaseous, liquid and/or solid fuels, the fuel is reacted with an oxidizing agent in a reaction space at a pressure of 10 to 120 bar and a reaction space temperature of 800 to 2,000° C. to obtain synthesis gas, wherein the oxidizing agent is introduced centrally in the upper region of the reaction space and wherein a flame is formed in the reaction space. The oxidizing agent is introduced into the reaction space separate from the fuel.