Disclosed is a production device and production method of electronic grade hydrofluoric acid. The method includes vaporizing the raw material industrial anhydrous hydrogen fluoride by an evaporator, transporting the vaporized hydrogen fluoride to a purification tower, obtaining a high purity hydrogen fluoride gas through rectification, transporting the high purity hydrogen fluoride gas to an absorption tower for absorption by a certain concentration of hydrofluoric acid in the liquid phase, obtaining the crude electronic grade hydrofluoric acid, and obtaining the electronic grade hydrofluoric acid product through ultrapure filtration. The disclosure overcomes the technical problems of small yield and low purity of the prior art. The production process meets the requirements of environmental protection. The disclosure is suitable for industrialized large-scale production.

The invention relates to a process for removing hydrogen sulfide and carbon dioxide from a feed gas stream. H2S in the feed gas stream is converted to elemental sulfur in a Claus unit. At least a part of the gas stream obtained is contacted with an aqueous lean absorbing medium in an absorption zone at a pressure between 0.9 and 2 bara. The aqueous lean absorbing medium used comprises one or more amines chosen from: a polyamine in the absence of tertiary amine functionalities having a pKa sufficient to neutralize carbamic acid, the polyamine having at least one primary amine functionality having a pKa smaller than 10.0 at 25 C., a polyamine in the absence of tertiary amine functionalities having a pKa sufficient to neutralize carbamic acid, the polyamine having at least one secondary amine functionality having a pKa for each sorbing nitrogen smaller than 10.0 at 25 C. The process is improved as compared to a process involving Claus off-gas treatment with (activated) MDEA. Effective CO2 removal is achieved while at the same time a simplified line-up with less equipment can be used.

The present invention relates to a process for producing an aqueous solution containing chlorine dioxide from gaseous chlorine dioxide and from an aqueous phase. The invention additionally relates to an apparatus for producing an aqueous solution containing chlorine dioxide and/or for carrying out the process of the invention. Finally, the invention also relates to the use of an apparatus according to the invention for carrying out a process according to the invention. In the following, all statements made in respect of the process of the invention also apply correspondingly to the apparatus of the invention and the use according to the invention, and vice versa, unless indicated otherwise in the individual case.

The invention pertains to processes for separating water from air. The processes may employ using an LCST solution with or without subsequent reverse osmosis, nanofiltration, or ultrafiltration.

A process for treating an H.sub.2S- and CO.sub.2-comprising fluid stream, in which a) the fluid stream is treated in a first absorber at a pressure of 10 to 150 bar with a first substream of a regenerated H.sub.2S-selective absorbent to obtain a treated fluid stream and an H.sub.2S-laden absorbent; b) the H.sub.2S-laden absorbent is heated by indirect heat exchange with regenerated H.sub.2S-selective absorbent; c) the heated H.sub.2S-laden absorbent is decompressed to a pressure of 1.2 to 10 bar in a low-pressure decompression vessel to obtain a first CO.sub.2-rich offgas and a partly regenerated absorbent; d) the partly regenerated absorbent is regenerated in a desorption column to obtain an H.sub.2S-rich offgas and regenerated absorbent; e) the H.sub.2S-rich offgas is fed to a Claus unit and the offgas from the Claus unit is fed to a hydrogenation unit to obtain hydrogenated Claus tail gas; f) the hydrogenated Claus tail gas and the first CO.sub.2-rich offgas are treated in a second absorber at a pressure of 1 to 4 bar with a second substream of the regenerated H.sub.2S-selective absorbent to obtain a second CO.sub.2-rich offgas and a second H.sub.2S-laden absorbent; and g) the second H.sub.2S-laden absorbent is guided into the first absorber. Also described is a plant suitable for performance of the process. The process is notable for a low energy requirement.

A gas purification device removes a part of ammonia contained in a first gas; recovers a first off-gas containing the removed ammonia, removes hydrogen sulfide and ammonia from a second gas produced by removing the part of ammonia, recovers a second off-gas containing the removed hydrogen sulfide and ammonia, and combusts the first off-gas and the second off-gas. The gas purification device includes: a first combustion chamber in which combustion is performed in a reducing atmosphere; a second combustion chamber in which combustion is performed in a reducing atmosphere downstream of the first combustion chamber; and a third combustion chamber in which combustion is performed in an oxidizing atmosphere downstream of the second combustion chamber. The first off-gas flows into the first combustion chamber and the second off-gas flows into the third combustion chamber.

A method with corresponding systems for reducing emission of amines to the atmosphere. The method includes a a) introducing a gas containing CO.sub.2 into an absorber; b) flowing the flue gas through an absorber having an absorbent with a water-lean solution having less than 50% water and one or more amines, with the absorbent capturing the CO.sub.2 and forming a reduced CO.sub.2 content gas having a baseline CO.sub.2 content; and c) washing the reduced CO.sub.2 content gas in a wash column with a wash solution comprising carbonic acid formed by addition of gaseous CO.sub.2 into the wash solution. In this method, the washing removes the amines from the reduced CO.sub.2 content gas and produces a reduced amine content gas exiting from the wash column.

A carbon dioxide capture system includes a first capture system and a second capture system. The first capture system including a first absorber that causes carbon dioxide contained in a combustion exhaust gas to be absorbed in a first absorbing liquid. The second capture system causes carbon dioxide contained in a combustion exhaust gas to be absorbed in a second absorbing liquid. The second rich liquid releases carbon dioxide at a lower temperature than the first rich liquid.

A still/stahl column includes a still section, a primary stahl section, the primary stahl section positioned beneath the still section, and a polishing stahl section, the polishing stahl section positioned beneath the primary stahl section. A process also includes feeding a water rich glycol still feed stream to the still section and feeding a stripping gas feed stream to the polishing still section. The process includes withdrawing a reboiler draw stream from the still section and heating the reboiler draw stream in a reboiler to form a reboiler inlet stream. The process includes injecting the reboiler inlet stream into the primary stahl section, stripping water from the water rich glycol with the stripping gas, and withdrawing a still stripping gas stream from a top portion of the still section. A lean glycol polishing discharge stream is withdrawn from a bottom portion of the polishing stahl section.

Systems and methods for removing CO2 from an ammonia stream using a warm water wash in a multi-stage water wash with varying temperatures.