Provided are a process and a system for treating both a high-pressure (HP) and a low-pressure (LP) acid gas-containing gas streams. The system includes a HP absorber unit, a flash drum coupled downstream of the HP absorber unit, and a LP absorber unit coupled downstream of the flash drum. The process includes introducing a HP rich amine solution from a HP absorber unit into a flash drum, operating the flash drum such that a flashed sour gas and a flash drum rich amine solution are produced, and introducing the flashed sour gas and the LP acid gas-containing gas stream into a LP absorber unit.

A desulfurization gas process includes water vapor, CO.sub.2 and SO.sub.x (x=2 and/or 3). In a treatment unit, the gas contacts a cooled alkaline aqueous solution having a temperature lower than an initial gas temperature, water and a carbonate of an alkali metal, to cool the gas, condense some water vapor and absorb SO.sub.x in the carbonate-containing solution, produce an SO.sub.x-depleted gas and an acidic aqueous solution including sulfate and/or sulfite ions. The SO.sub.x-depleted gas and a portion of the acidic aqueous solution can then be withdrawn from the treatment unit. Carbonate of the alkali metal can be added to remaining acidic aqueous solution to obtain a made-up alkaline aqueous solution. This solution can be cooled and reused as the cooled alkaline aqueous solution. An SO.sub.x absorbent solution includes a bleed stream from a CO.sub.2-capture process, sodium or potassium carbonate, and an acidic aqueous solution obtained from desulfurization.

The present invention relates to a process for removing carbon dioxide from synthesis gas using a hygroscopic, physical absorption medium. The process includes cooling the absorption medium and the synthesis gas; water is at least partially removed from the synthesis gas by condensation; carbon dioxide is removed from the cooled synthesis gas via the cooled absorption medium in a physical absorption step at elevated pressure; laden absorption medium is treated in a plurality of serially arranged flash stages, wherein co-absorbed carbon monoxide and hydrogen are removed from the laden absorption medium in at least one first flash stage, and carbon dioxide is removed from the laden absorption medium in a flash stage arranged downstream of the first flash stage. The process features a high rate of separated carbon dioxide and a pure and dry (anhydrous) carbon dioxide product. The invention further relates to a plant for performing the process.

The present invention relates to a process for producing hydrogen and for separating carbon dioxide from synthesis gas using a physical absorption medium. The process comprises the steps where the synthesis gas and the absorption medium are cooled; carbon dioxide is removed from the cooled synthesis gas via the cooled absorption medium in a physical absorption step at elevated pressure; laden absorption medium is treated in a plurality of flash stages, wherein co-absorbed carbon monoxide, hydrogen and carbon dioxide are separately removed from the laden absorption medium; hydrogen is separated from synthesis gas freed of carbon dioxide in a physical separation step, wherein hydrogen as product gas and an offgas comprising hydrogen, carbon monoxide and carbon dioxide are obtained; product gas hydrogen and carbon dioxide are discharged from the process. The invention further relates to a plant for performing the process.

An apparatus for purifying gas where gas is treated in a multistage treatment having at least two ejector stages, a motive medium including liquid, steam or gaseous agent at high pressure injected by an ejector of the ejector stage, and the gas is sucked into the same ejector and mixed with the motive medium for forming a mixture, at least a part of gas and/or liquid phase of the mixture is supplied to a second ejector stage having so that a second motive medium which includes liquid, steam or gaseous agent is injected to the ejector and the gas and/or the liquid phase is sucked into the same ejector in which the gas and/or liquid phase is mixed with the second motive medium for forming a second mixture, at least one of the mixtures includes an additive for removing impurities of the gas, and a purified gas is formed.

Disclosed herein is a rotating packed bed, RPB, arrangement configured to provide mass transfer between a liquid sorbent and a gas, the RPB arrangement comprising: an RPB configured to provide a substantial cross-flow between a liquid sorbent and a gas; and a spray arranged to spray the liquid sorbent onto the RPB; wherein the RPB and spray are both arranged at different longitudinal positions on a gas flow path through the RPB arrangement.

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.

A desulfurization gas process includes water vapor, CO.sub.2 and SO.sub.x (x=2 and/or 3). In a treatment unit, the gas contacts a cooled alkaline aqueous solution having a temperature lower than an initial gas temperature, water and a carbonate of an alkali metal, to cool the gas, condense some water vapor and absorb SO.sub.x in the carbonate-containing solution, produce an SO.sub.x-depleted gas and an acidic aqueous solution including sulfate and/or sulfite ions. The SO.sub.x-depleted gas and a portion of the acidic aqueous solution can then be withdrawn from the treatment unit. Carbonate of the alkali metal can be added to remaining acidic aqueous solution to obtain a made-up alkaline aqueous solution. This solution can be cooled and reused as the cooled alkaline aqueous solution. An SO.sub.x absorbent solution includes a bleed stream from a CO.sub.2-capture process, sodium or potassium carbonate, and an acidic aqueous solution obtained from desulfurization.

The invention relates to a process and plant for purifying a raw synthesis gas containing hydrogen and carbon monoxide as target components and carbon dioxide and sulfur components as disruptive components by gas scrubbing with a physically acting, liquid scrubbing medium selective for carbon dioxide and sulfur components. The process/the plant comprise an absorption apparatus, a hot regeneration apparatus, a preferably multistage flash regeneration apparatus and a reabsorber column supplied with the first portion of a stripping gas. According to the invention the flash regeneration apparatus is supplied with the second portion of the stripping gas.

The present invention relates to a cleaning apparatus (100) for metal smallware, comprising: a washing chamber (1) apt to receive a solvent and at least one batch of metal smallware soiled with lubricant and configured to carry out a washing cycle to remove at least part of said lubricant from said batch of metal smallware soiled with lubricant by means of said solvent and; suction means (2) connected to said washing chamber (1) and configured to carry out a discharge cycle by sucking said gaseous mixture comprising air and solvent from said washing chamber (1); a main absorption column (4) having a first side (41) and a second side (42) opposite each other, and wherein said first side (41) is hydraulically connected to said suction means (2) so as to receive said gaseous mixture comprising air and solvent and said second side (42) is hydraulically connected to a supply duct (3) so as to receive an absorption liquid from the latter.

In particular, the main absorption column (4) is configured to cause an interaction between a gaseous mixture supplied by said suction means (2) and an absorption liquid supplied by said supply duct (3) so as to perform chemical absorption of a solvent present in said gaseous mixture comprising air and solvent, in said absorption liquid, and therefore reduce the concentration of solvent in the gaseous mixture comprising air and solvent.