Abstract: A process for removing impurities, in particular oxides of sulphur (SOx) and/or oxides of nitrogen (NOx) from oxygen-containing gas streams by scrubbing with at least one washing agent is described. In order to achieve effective gas purification in an economical manner even in the case of so-called large “oxyfuel” furnaces which operate with oxygen as fuel gas, it is proposed to convert the impurities at an elevated pressure of at least 2 bar with at least one basic constituent of the washing agent into salts and to wash out said impurities as dissolved salts.

Abstract: The present invention relates to a method for preparing linear alpha-olefins by oligomerizing of ethylene in the presence of a first organic solvent and a homogenous catalyst in a reactor, characterized in that the reactor overhead is cooled by means of a refrigerant.

Abstract: The invention relates to a process for the removal of NO and NO2 from an oxygen-containing gas stream, which comprises a scrubbing step in which the gas stream is brought into contact with an ammonia-containing scrubbing solution, NO is oxidized to form NO2 by means of the oxygen present at a pressure of at least 2 bar and temperatures of from 15° C. to 60° C. and at least part of the NO2 present in the gas stream is converted by means of the ammonia-containing scrubbing solution into ammonium nitrite and a downstream decomposition step in which the ammonium nitrite present in the scrubbing solution is thermally decomposed into elemental nitrogen and water, where the decomposition step is carried out at temperatures of from 121° C. to 190° C. and a pressure of from 2 to 40 bar. The invention likewise relates to a plant for operation of the process of the invention.

Abstract: The invention relates to a process for the removal of NO and NO2 from an oxygen-containing gas stream, which comprises a scrubbing step in which the gas stream is brought into contact with an ammonia-containing scrubbing solution, NO is oxidized to form NO2 by means of the oxygen present at a pressure of at least 2 bar and temperatures of from 15° C. to 60° C. and at least part of the NO2 present in the gas stream is converted by means of the ammonia-containing scrubbing solution into ammonium nitrite and a downstream decomposition step in which the ammonium nitrite present in the scrubbing solution is thermally decomposed into elemental nitrogen and water, where the decomposition step is carried out at temperatures of from 121° C. to 190° C. and a pressure of from 2 to 40 bar. The invention likewise relates to a plant for operation of the process of the invention.

Abstract: A method and device for the catalytic decomposition of laughing gas in a laughing-gas-bearing gas. The method includes diluting the laughing-gas-bearing gas with a diluting gas, while forming a laughing-gas-bearing charge gas. The laughing-gas bearing charge gas is passed through a heat-exchange step where heat exchange occurs with an exhaust. A heating step occurs for occasional heating of the laughing-gas-bearing charge gas in a fixed-bed reactor for catalytic decomposition of the laughing gas. In some embodiments the diluting gas is dried, and at least a part of the exhaust from the catalytic decomposition of the laughing gas is mixed with the laughing-gas-bearing charge gas upstream of the catalytic decomposition of the laughing gas.

Abstract: A device and method for the decomposition of laughing gas including a gas inlet for supplying a laughing-gas-bearing gas; a first heat-exchanger for the exchange of heat between an exhaust and the laughing-gas-bearing gas; a heating device for occasional heating of the laughing-gas-bearing gas and a fixed-bed reactor in which a catalyst is included in order to decompose the laughing gas. The device also includes a gas outlet, through which exhaust leaving the fixed-bed reactor can be taken away through the heat exchanger. The device may be used to implement a method where the catalyst for decomposition of laughing gas is maintained at temperatures below 800° C. and in which the fixed-bed reactor is arranged as an adiabatic reactor.

Abstract: The invention relates to a process for preparing linear ?-olefins, wherein ethylene 1a is conducted into the oligomerization reactor 2 in the liquid phase. The oligomerization reactor 2 has a mechanical stirrer 2a in order to ensure optimal mixing of the liquid ethylene and of the catalyst in the liquid phase. From the top of the oligomerization reactor 2, vaporized ethylene is drawn off together with light ?-olefins and a small proportion of the organic solvent. The gas mixture drawn off from the top of the reactor 2 is condensed together with gaseous fresh ethylene 7 by means of heat exchanger 3 and separator 4. The liquid phase drawn off from the separator 4 is conducted by means of circulation pump 5a as liquid ethylene input 1a back into the oligomerization reactor 2. The liquid products of the oligomerization reaction are drawn off 8 laterally from the base of the reactor 2.

Abstract: The invention relates to a process for the treatment of a used waste alkali, in which the used waste alkali is oxidized at a superatmospheric pressure in the range from 60 bar to 200 bar. The pressure of the used waste alkali L is increased and then heated by indirect heat exchange. The heated used waste alkali is conveyed into a separator, wherein vaporized aqueous phase is separated from the used waste alkali. The resultant liquid phase is brought to the desired reaction pressure and introduced into an oxidation reactor. In the oxidation reactor, the used waste alkali is oxidized. In a first reaction, thiosulphates are formed from the sulphides. In a second reaction, the thiosulphates are converted into more stable sulphates.

Abstract: The laughing-gas-containing gas (1) is diluted by means of a diluting gas (2). The diluting gas (2) is virtually free from water fractions in the dryer (3). After feed of the diluting gas (2) via the feed line (13), exhaust gas (8) from the catalytic decomposition (7) is added (4) to the laughing-gas-containing feed gas (12). After addition (4) of the exhaust gas (8) from the catalytic decomposition of laughing gas (7), the laughing-gas-containing feed gas (12) is compressed (5) and passed to the heat exchanger (6). In the heat exchanger (6) the laughing-gas-containing feed gas (12) is preheated by heat exchange with the exhaust gas (8). The exhaust gas (8) is cooled in the heat exchanger (6) in this process. The preheated laughing-gas-containing feed gas (12) is passed via a further optional heater (11) as a feed to the catalytic laughing gas decomposition (7). In order to avoid a concentration build-up, some of the exhaust gas (8) is passed out (9) of the process.

Abstract: The invention relates to an apparatus and to a process for decomposing dinitrogen monoxide. The apparatus comprises a gas inlet 1 for supplying a nitrogen monoxide-containing gas, a first heat exchange medium 3 for exchanging heat between an offgas and the nitrogen monoxide-containing gas, a heating apparatus 4 for occasional heating of the nitrogen monoxide-containing gas, a fixed bed reactor 5 in which a catalyst is accommodated, in order to decompose the dinitrogen monoxide in the dinitrogen monoxide-containing gas, a gas outlet through which the offgas leaving the fixed bed reactor can be conducted out via the heat exchange medium 3. According to the invention, the catalyst is suitable for decomposing dinitrogen monoxide at temperatures below 800° C., especially preferably below 450° C., more preferably below 400° C. The fixed bed reactor 5 is configured for operation in an adiabatic state.

Abstract: The present invention relates to a method and a reactor system, for the oligomerization of ethylene, comprising oligomerizing ethylene in a reactor in the presence of a solvent and a catalyst composition to produce a liquid product stream comprising linear alpha-olefins, solvent and catalyst composition, and deactivating and extracting the catalyst composition in said liquid product stream by mixing it with a polar phase in a dynamic mixing device having rotor and stator elements comprising concentric tool rings.

Abstract: The present invention relates to a method for preparing linear alpha-olefins (LAO) by oligomerization of ethylene in the presence of solvent and homogenous catalyst, comprising the steps of: (i) feeding ethylene, solvent and catalyst into an oligomerization reactor, (ii) oligomerizing the ethylene in the reactor, (iii) removing a reactor outlet stream comprising solvent, linear alpha-olefins, ethylene, and catalyst from the reactor via a reactor outlet piping system, (iv) transferring the reactor outlet stream to a catalyst deactivation and removal step, and (v) deactivating and removing the catalyst from the reactor outlet stream, characterized in that at least one organic amine is added into the oligomerization reactor and/or into the reactor outlet piping system.

Abstract: The present invention relates to a method for preparing linear alpha-olefins by oligomerizing of ethylene in the presence of a first organic solvent and a homogenous catalyst in a reactor, characterized in that the reactor overhead is cooled by means of a refrigerant.

Abstract: The present invention relates to a method for preparing linear alpha-olefins by oligomerizing of ethylene in the presence of an organic solvent and a homogenous catalyst, characterized in that the method is carried out in a reactor being fed with a gaseous feed comprising a minor amount of ethylene and a major amount of an inert gas.

Abstract: A process and apparatus for producing a hydrogen-containing product gas (4) from a glycerol-containing feedstock (1). A product gas (4) is produced from the glycerol-containing feedstock (1) by separation of undesirable substances (V) and the pyrolysis of glycerol (P).

Abstract: The invention relates to a process as well as a device for continuous thermal decomposition (pyrolysis) of a mixture of substances (crude glycerol) (1) that contains glycerol, salts and water, whereby the crude glycerol (1) is heated in a reactor (pyrolysis reactor) (R) to a temperature (pyrolysis temperature) of more than 100° C. The pyrolysis of the crude glycerol (1) is performed at a pressure (pyrolysis pressure) that is higher than the vapor pressure of the water, present in the pyrolysis reactor (R), at pyrolysis temperature, and salts and other higher-boiling substances together with water are drawn off continuously from the pyrolysis reactor (R) as waste water (3).