Abstract: The present invention relates to a continuous process for the preparation of a zeolitic material comprising SiO2 in its framework structure, said process comprising (i) continuously preparing a mixture comprising one or more solvents, one or more structure directing agents, and one or more sources of SiO2; (ii) continuously feeding the mixture prepared in (i) into one or more continuous flow reactors; and (iii) heating the mixture in the one or more continuous flow reactors for continuously obtaining a zeolitic material comprising SiO2 in its framework structure; wherein the mixture contained in the one or more continuous flow reactors is subject to a pulsatile flow regime. The present invention also relates to a zeolitic material as obtainable and/or obtained according to said process and the use of the zeolite material as a molecular sieve, as an adsorbent, for ion-exchange, or as a catalyst and/or as a catalyst support.

Abstract: The present invention relates to a process for the preparation of a zeolitic material, as well as to a catalyst per se as obtainable or obtained according to said process. Furthermore, the present invention relates to the use of the zeolitic material, in particular as a catalyst.

Abstract: Process for precipitating a carbonate or (oxy)hydroxide comprising nickel from an aqueous solution of a nickel salt wherein such process is carried out in a vessel comprising (A) a vessel body, (B) one or more elements that control the hydraulic flow of the slurry formed during the precipitation and that induce a loop-type circulation flow, and (C) a stirrer whose stirrer element is in the vessel but located separately from the element(s) (B).

Abstract: The invention relates to a jet mill comprising a milling chamber with a longitudinal axis, an inlet at one end of the axis and an outlet at the opposite end of the axis, the milling chamber comprising a multitude of pins arranged in the free flow cross-section of the milling chamber, wherein the pins are arranged in at least two planes perpendicular to the longitudinal axis, the planes being distant to each other in the longitudinal direction, and the pins of one plane being laterally offset to the pins of the subsequent plane, wherein the milling chamber is divided into alternate pin segments and acceleration segments, the pin segments each having at least two planes of pins, and the acceleration segments having no pins.

Abstract: Disclosed herein is a continuous process for preparing zeolitic material with a CHA-type framework structure comprising SiO2 and X2O3 and the zeolitic material so-obtained. The processes comprises (i) preparing a mixture comprising one or more sources of SiO2, one or more sources of X2O3, seed crystals, one or more tetraalkylammonium cation R5R6R7R8N+-containing compounds as structure directing agent, and a liquid solvent system; (ii) continuously feeding the mixture prepared in (i) into a continuous flow reactor at a liquid hourly space velocity; and (iii) crystallizing the zeolitic material with a CHA-type framework structure from the mixture in the continuous flow reactor.

Abstract: Process for precipitating a mixed hydroxide of TM wherein TM comprises Ni and at least one of Co and Mn and, optionally, Al, Mg, Zr or Ti, from an aqueous solution of salts of such transition metals or of Al or of Mg, wherein such process is carried out in a stirred vessel and comprises the step of introducing an aqueous solution of alkali metal hydroxide and an aqueous solution of transition metal salts through at least two inlets into said stirred vessel wherein the distance of the locations of introduction of salts of TM and of alkali metal hydroxide is equal or less than 6 times the hydraulic diameter of the tip of the inlet pipe of the alkali metal hydroxide.

Abstract: Disclosed herein is a continuous process for preparing zeolitic material with a CHA-type framework structure comprising SiO2 and X2O3 and the zeolitic material so-obtained. The processes comprises (i) preparing a mixture comprising one or more sources of SiO2, one or more sources of X2O3, seed crystals, one or more tetraalkylammonium cation R5R6R7R8N+-containing compounds as structure directing agent, and a liquid solvent system; (ii) continuously feeding the mixture prepared in (i) into a continuous flow reactor at a liquid hourly space velocity; and (iii) crystallizing the zeolitic material with a CHA-type framework structure from the mixture in the continuous flow reactor.

Abstract: Process for precipitating a carbonate or (oxy)hydroxide comprising nickel from an aqueous solution of a nickel salt wherein such process is carried out in a vessel comprising (A) a vessel body, (B) one or more elements that control the hydraulic flow of the slurry formed during the precipitation and that induce a loop-type circulation flow, and (C) a stirrer whose stirrer element is in the vessel but located separately from the element(s) (B).

Abstract: The present invention relates to a process for the preparation of a zeolitic material, as well as to a catalyst per se as obtainable or obtained according to said process. Furthermore, the present invention relates to the use of the zeolitic material, in particular as a catalyst.

Abstract: A process for removing acid gases from a water vapor-containing fluid stream comprises a) providing an absorption liquid which is incompletely miscible with water; b) treating the fluid stream in an absorption zone with the absorption liquid to obtain an acid gas-depleted treated fluid stream and an acid gas-loaded absorption liquid; c) directing the treated fluid stream to a rehydration zone and treating the fluid stream with an aqueous liquid to volatilize at least part of the aqueous liquid; d) regenerating the loaded absorption liquid to expel the acid gases at least in part and obtain a regenerated absorption liquid, and directing the regenerated absorption liquid to step b); and e) separating, from the absorption liquid, an aqueous liquid that has condensed in the absorption zone, and directing the aqueous liquid to step c). The process allows for an efficient removal of water accumulated in the absorption liquid system.

Abstract: A process for removing sulphur oxides from a fluid stream, such as flue gas, comprising: providing a non-aqueous absorption liquid containing at least one hydrophobic amine, the liquid being incompletely miscible with water; treating the fluid stream in an absorption zone with the non-aqueous absorption liquid to transfer at least part of the sulphur oxides into the non-aqueous absorption liquid and to form a sulphur oxide-hydrophobic amine-complex; causing the non-aqueous absorption liquid to be in liquid-liquid contact with an aqueous liquid whereby at least part of the sulphur oxide-hydrophobic amine-complex is hydrolyzed to release the hydrophobic amine and sulphurous hydrolysis products, and at least part of the sulphurous hydrolysis products is transferred into the aqueous liquid; separating the aqueous liquid from the non-aqueous absorption liquid. The process mitigates absorbent degradation problems caused by sulphur dioxide and oxygen in flue gas.

Abstract: A process for removing sulphur oxides from a fluid stream, such as flue gas, that comprises a) providing a non-aqueous absorption liquid containing at least one hydrophobic amine, the non-aqueous absorption liquid being incompletely miscible with water: b) treating the fluid stream in an absorption zone with the non-aqueous absorption liquid to transfer at least part of the sulphur oxides into the non-aqueous absorption liquid and to form a sulphur oxide-hydrophobic amine-complex: c) causing the non-aqueous absorption liquid to be in liquid-liquid contact with an aqueous liquid whereby at least part of the sulphur oxide-hydrophobic amine-complex is hydrolyzed to release the hydrophobic amine and sulphurous hydrolysis products, and at least part of the sulphurous hydrolysis products is transferred into the aqueous liquid; d) separating the aqueous liquid from the non-aqueous absorption liquid. The process mitigates absorbent degradation problems caused by sulphur dioxide and oxygen in flue gas.

Abstract: A process for removing acid gases from a water vapour-containing fluid stream comprises a) providing an absorption liquid which is incompletely miscible with water; b) treating the fluid stream in an absorption zone with the absorption liquid to obtain an acid gas-depleted treated fluid stream and an acid gas-loaded absorption liquid; c) directing the treated fluid stream to a rehydration zone and treating the fluid stream with an aqueous liquid to volatilize at least part of the aqueous liquid; d) regenerating the loaded absorption liquid to expel the acid gases at least in part and obtain a regenerated absorption liquid, and directing the regenerated absorption liquid to step b); and e) separating, from the absorption liquid, an aqueous liquid that has condensed in the absorption zone, and directing the aqueous liquid to step c). The process allows for an efficient removal of water accumulated in the absorption liquid system.

Abstract: An absorption medium for removing acid gases from a fluid stream comprises an aqueous solution (A) of an alkali metal salt of an N,N-di-C1-C4-alkylaminocarboxylic acid and (B) N-hydroxyethylpiperazine. The absorption medium has a low vapor pressure and an increased resistance to oxygen. Preferred fluid streams are combustion exhaust gases or biogas.

Abstract: An absorption medium for removing acid gases from a fluid stream comprises an aqueous solution of a) of at least one metal salt of an aminocarboxylic acid, and b) of at least one acid promoter, wherein the molar ratio of b) to a) is in the range from 0.0005 to 1.0. The acid promoter is selected from mineral acids, carboxylic acids, sulfonic acids, organic phosphonic acids and partial esters thereof. The absorption medium, compared with absorption media based on amino acid salts, has a reduced regeneration energy requirement without significantly reducing the absorption capacity of the solution for acid gases. In a process for removing acid gases from the fluid stream, the fluid stream is brought into contact with the absorption medium.

Abstract: An absorption medium for the removal of acid gases from a fluid stream comprises an aqueous solution a) of at least one amine and b) at least one phosphonic acid, wherein the molar ratio of b) to a) is in the range from 0.0005 to 1.0. The phosphonic acid is, e.g., 1-hydroxyethane-1,1-diphosphonic acid. The absorption medium exhibits a reduced regeneration energy requirement compared with absorption media based on amines or amine/promoter combinations, without significantly decreasing the absorption capacity of the solution for acid gases.

Abstract: An absorption medium for removing acid gases from a fluid stream comprises an aqueous solution (A) of an alkali metal salt of an N,N-di-C1-C4-alkylaminocarboxylic acid and (B) N-hydroxyethylpiperazine. The absorption medium has a low vapor pressure and an increased resistance to oxygen. Preferred fluid streams are combustion exhaust gases or biogas.

Abstract: An absorption medium for the removal of acid gases from a fluid stream comprises an aqueous solution a) of at least one amine and b) at least one phosphonic acid, wherein the molar ratio of b) to a) is in the range from 0.0005 to 1.0. The phosphonic acid is, e.g., 1-hydroxyethane-1,1-diphosphonic acid. The absorption medium exhibits a reduced regeneration energy requirement compared with absorption media based on amines or amine/promoter combinations, without significantly decreasing the absorption capacity of the solution for acid gases.

Abstract: An absorption medium for removing acid gases from a fluid stream comprises an aqueous solution of a) of at least one metal salt of an aminocarboxylic acid, and b) of at least one acid promoter, wherein the molar ratio of b) to a) is in the range from 0.0005 to 1.0. The acid promoter is selected from mineral acids, carboxylic acids, sulfonic acids, organic phosphonic acids and partial esters thereof. The absorption medium, compared with absorption media based on amino acid salts, has a reduced regeneration energy requirement without significantly reducing the absorption capacity of the solution for acid gases. In a process for removing acid gases from the fluid stream, the fluid stream is brought into contact with the absorption medium.