Abstract: Ammonia is catalytically produced from a nitrogen-hydrogen mixture. First of all, a vaporous feed mixture, which comprises 30 to 60 vol-% methanol and 40 to 70 vol-% steam and has a volume ratio steam:methanol of 1 to 3, is passed through at least one bed of a breakdown catalyst at pressures in the range from 30 to 200 bar, the temperatures in the catalyst bed lying in the range from 200 to 500° C. From the catalyst bed, a first gas mixture is withdrawn, which, calculated dry, comprises 40 to 80 vol-% H2 and 10 to 30 vol-% CO2. The first gas mixture is cooled, CO2 is removed in a gas cleaning, and a second gas mixture is generated, which comprises at least 95 vol-% nitrogen and hydrogen, and which is supplied as synthesis gas to an ammonia synthesis for the catalytic production of ammonia.

Abstract: In the presence of a catalyst, at least one isoparaffin having 4 to 6 C atoms per molecule is reacted with at least one olefin having 2 to 6 C atoms per molecule in a liquid phase to obtain a product containing alkylate, a suspension containing isoparaffin and a granular zeolite catalyst being supplied to the upper region of a reaction column. Below the point where the catalyst-containing suspension is supplied, an isoparaffin-olefin mixture is introduced into the reaction column, the temperatures in the reaction column being maintained in the range from 50 to 120° C. From the bottom region of the reaction column a product mixture containing alkylate is withdrawn, and in a separation by distillation alkylate product is recovered therefrom. Preferably, isoparaffin and catalyst are recovered from the separation by distillation and at least partly recirculated to the upper region of the reaction column.

Abstract: A process for catalytically generating organic substances by partial oxidation of an organic feedstock in the presence of molecular oxygen at temperatures in the range from 200 to 500° C. in at least one cooling-tube reactor, wherein 40 to 100 wt-% of the total amount of catalyst is disposed as a coating on the outside of the cooling tubes.

Abstract: A process for producing propylene from methanol, wherein methanol vapor is reacted on a first catalyst to obtain a first vapor mixture containing dimethyl ether (DME), which is reacted on a form-selective zeolite catalyst disposed as bed in at least two series-connected shaft reactors to produce a product mixture containing propylene.

Abstract: Process for generating a homogeneous gas mixture of o-xylene and air for the production of phthalic anhydride wherein o-xylene is completely evaporated in the absence of oxygen, superheated and then mixed with air and supplied to a phthalic anhydride reactor.

Abstract: This invention relates to a process of producing C2- to C4-olefins from steam and a feed mixture containing C4- to C8-olefins, wherein the feed mixture containing steam is introduced into a reactor with an inlet temperature of 300 to 700° C., said reactor comprising a bed of granular, form-selective zeolite catalyst, and wherein a product mixture containing steam and C2- to C4-olefins is withdrawn from the bed and is passed through at least one cooling means.

Abstract: Residual oil from the processing of crude oil, natural bitumen or oil sand is mixed in a mixer with granular, hot coke as heat carrier (heat carrier coke) in a weight ratio of 1:3 to 1:30, where on the granules of the heat carrier coke there is first of all formed a liquid residue film which partly evaporates in the mixer. Gases and vapors and moist, sticky coke are withdrawn from the mixer. The mixture of coke and residual oil is introduced into a subsequently connected stirred tank in which the mixture slowly moves downwards while being stirred mechanically at a temperature of 450 to 600° C. and preferably at 480 to 550° C. Dry, flowable coke is withdrawn from the stirred tank. Usually, the dwell time of the heat carrier coke in the stirred tank is 1 to 30 minutes.

Abstract: The solids will first of all reach a first container under atmospheric pressure and then reach a second container of variable pressure, which is disposed thereunder, before they are introduced into the pressure vessel. The first and the second container each have a lower outlet passage and a movable shutter cooperating with the outlet passage. The outlet end of the outlet passage is disposed 20 to 400 mm above the shutter in the closed position, in the closed position the shutter forms the bottom of a chamber at least partly filled with solids. The chamber is connected with the outlet passage in a gastight way, and there is no gastightness between the chamber and the shutter. In the closed position, the shutter carries a solid bed, a vertical solid column having a height of at least 1 m is present in the outlet passage and in the container. In the closed position, seal gas is pressed into the chamber and into the solid column from the outside.

Abstract: A material containing combustible components is burned or gasified in a circulating fluidized bed comprising a turbulence chamber, a solids separator connected to the upper area of the turbulence chamber, a return line leading from the solids separator to the turbulence chamber and a cooling device for the indirect cooling of solids arriving from the solids separator. The cooling device comprises several fluidized beds through which the solids pass one after the other. The first fluidized bed, into which the hot solids arriving from the solids separator are introduced first, is situated in a dechlorinating chamber.

Abstract: An electrolyte line extends from the outlet of an electrolysis device to a collecting tank and from the same back to the inlet of the electrolysis device. The electrolyte is passed from the outlet of the electrolysis device to a first container which is disposed at a higher level than a second container. Electrolyte collected in the first container is periodically discharged through a first syphon line into the second container, and electrolyte collected in the second container is periodically discharged through a second syphon line into the collecting tank which is disposed at a lower level than the second container. The outlet end of each syphon line is disposed at a distance above the liquid level of the container disposed thereunder, so that electrolyte always flows only in one of the two syphon lines or in none of the syphon lines. When electrolyte flows in none of the two syphon lines, electrolyte is preferably supplied from the collecting tank into the second container.

Abstract: The electrolytic cell has a trough-like container with a bottom, with side walls and with at least one inlet and at least one outlet for the electrolyte. Numerous plate-like electrodes are disposed in the container and are partly immersed in an electrolyte bath. The bottom of the container which is in contact with the electrolyte bath has numerous openings for the passage of electrolyte, and below the bottom there is disposed at least one distribution chamber for recirculated electrolyte. At least one of the side walls of the container is equipped with at least one recirculation chamber for recirculating electrolyte from the electrolyte bath into the distribution chamber, the upper portion of the recirculation chamber being connected with the electrolyte bath and the lower portion of the recirculation chamber communicating with the distribution chamber.

Abstract: Ammonia is recovered from waste water containing NH3, at least one acid gas (CO2, H2S) and inert gases. Firstly, the waste water is passed through a pretreatment column and then, at least in part, into a total stripping column. The top product from the total stripping column is cooled in a condenser, and an aqueous NH3-containing condensate coming from the condenser is fed to an NH3 stripping column. The top product from the NH3 stripping column is brought into direct contact with circulating aqueous NH3-containing condensate in a wash column, and NH3 is recovered from the top product from the wash column. Some of the bottom product from the wash column is fed back into the NH3 stripping column. The temperature in the bottom region of the pretreatment column is set to from less than 30 to 200° C., a sub-stream of the waste water is introduced into the upper region of the pretreatment column, and a second sub-stream of the waste water is fed into the pretreatment column below the first sub-stream.

Abstract: The electrolyte is supplied from a reservoir through at least one supply line to an electrolysis area including anodes and cathodes and at least one electric d.c. voltage source, and used electrolyte is at least partly recirculated from the electrolysis area back to the reservoir through at least one discharge line. Between a first contact point in the electrolyte of the supply line and a second contact point in the electrolyte of the discharge line there is a bridge line containing electrolyte, where the ohmic resistance R1 of the electrolyte in the bridge line between the first and the second contact point is not more than 10% of the ohmic resistance R2 which exists between the first and the second contact point in the electrolyte flowing through the reservoir. The amount of electrolyte flowing through the bridge line per unit time is not more than 5% of the amount of electrolyte flowing in the supply line in the vicinity of the first contact point.

Abstract: The oil seed is first of all comminuted and then formed into flakes by means of rolling, before it is supplied to the recovery of oil. The flakes are charged into a transporting mixer, to which steam and/or water are supplied at the same time, and the flakes in the mixer are transported to the outlet of the mixer with a dwell time of 5 to 50 seconds. With a moisture content of 8 to 20 wt-% and with temperatures in the range from 90 to 110° C., the flakes are withdrawn from the mixer and passed through an annealing zone, in which the flakes are moved over heated trays with dwell times of 15 to 50 minutes and temperatures in the range from 90 to 110° C. The flakes are withdrawn from the annealing zone with a residual moisture which still amounts to at least half the moisture content at the inlet of the annealing zone, and are passed through a drying and cooling zone in which the flakes are converted to granules which are supplied to the recovery of oil.

Abstract: Granular coal and preheated granular iron ore are charged into a low-temperature carbonization reactor, in which temperatures in the range from 800 to 1050 ° C. are produced by supplying gas containing oxygen and by partial oxidation of the components of the coal. In the low-temperature carbonization reactor, the granular solids are maintained in a turbulent movement. From the upper region of the reactor, hot exhaust gas is supplied to a solids separator. The granular iron ore is preheated by means of the hot exhaust gas and hot, granular mixture of iron ore and low-temperature coke is withdrawn as product from the reactor and/or from the separator. The low-temperature carbonization reactor may be designed as fluidized-bed reactor or as pneumatic conveyor section. The granular mixture of iron ore and low-temperature coke is suitable e.g. for a melt reduction process.

Abstract: An electrolyte line extends from the outlet of an electrolysis device to a collecting tank and from the same back to the inlet of the electrolysis device. The electrolyte is passed from the outlet of the electrolysis device to a first container which is disposed at a higher level than a second container. Electrolyte collected in the first container is periodically discharged through a first syphon line into the second container, and electrolyte collected in the second container is periodically discharged through a second syphon line into the collecting tank which is disposed at a lower level than the second container. The outlet end of each syphon line is disposed at a distance above the liquid level of the container disposed thereunder, so that electrolyte always flows only in one of the two syphon lines or in none of the syphon lines. When electrolyte flows in none of the two syphon lines, electrolyte is preferably supplied from the collecting tank into the second container.