An acid-gas capturing apparatus according to an embodiment includes an absorption unit configured to discharge an absorption-unit exhaust gas, and a regeneration unit configured to discharge a regeneration unit exhaust gas. The regeneration unit exhaust gas is compressed in a compression unit. The absorption-unit exhaust gas or the regeneration unit exhaust gas before it is compressed by the compression unit is cleaned in a first cleaning unit by means of a first cleaning liquid. A compression-condensate liquid, which is generated by the compression of the regeneration unit exhaust gas in the compression unit, is mixed into the first cleaning liquid through a first compression-condensate-liquid line whose one end is connected to the compression unit.

A process for operating an oxidizable combustion gas cleaning unit in a metallurgical plant, including the steps of: (a) passing an oxidizable combustion gas from a metallurgical reactor, in particular a blast furnace gas from a blast furnace, in a packed bed scrubber arrangement through a packed bed in countercurrent with a washing water or in a spray scrubber arrangement to remove cyanide compounds, in particular hydrogen cyanide, and to increase the removal of chloride compounds, in particular hydrogen chloride, from the combustion gas by solubilizing the cyanide and chloride compounds in the washing water, (b) collecting the washing water containing solubilized cyanide and chloride compounds at a bottom end of the packed bed or spray scrubber arrangement, and (c) collecting a cleaned oxidizable combustion gas at a top of the packed bed or spray scrubber arrangement, wherein a base is added to the washing water before step (a).

A device and process for removing vapors from a gas is disclosed. A tower is provided. Sub-cooled pellets are distributed by the solids distributor across a horizontal cross-section of the tower. A process gas, comprising a product vapor, passes through the gas inlet. The product vapor and the sub-cooled pellets comprise the same material. The product vapor and the sub-cooled pellets agglomerate as the product vapor desublimates onto the sub-cooled pellets, forming product pellets and a vapor-depleted gas. A crushing device, a screening device, and a solids heat exchanger are provided. A portion of the product pellets are recycled as sub-cooled pellets to the solids distributor by crushing and screening the portion of the product pellets to the size distribution of the sub-cooled pellets and cooling the portion of the product pellets to produce the sub-cooled pellets.

The present invention provides a gel containing a crosslinked polymer having at least one selected from the group consisting of an acidic dissociative group, an acidic dissociative group in a salt form, and a derivative group of an acidic dissociative group, and a condensate of a compound represented by the following formula (I): Si{R.sup.1N(R.sup.2)(R.sup.3)}(OR.sup.4)(OR.sup.5)(R.sup.6) (wherein each group is as defined in the DESCRIPTION).

A process for forming a solid product or products is disclosed. The process is provided with n desublimating exchangers. An exchanger E1 being associated with a first exchanger and an exchanger En being associated with an nth exchanger, n representing the number of exchangers. The n exchangers comprise at least one direct-contact exchanger comprising a contact fluid. A process fluid is passed through the n exchangers in order from E1 through En. The process fluid comprises a product component or components. The solid product or products form from the product component or components in the plurality of exchangers by desublimation. The solid product or products are separated from the process fluid. In this manner, a solid product or products is formed.

The invention relates to a cleaning device for separating an organic isocyanate produced by the reaction of an organic amine with a stoichiometric excess of phosgene in the gas phase from the gaseous raw product obtained in the reaction, said device comprising a first separating body comprising at least one raw product supply line for a gaseous raw product flow containing at least the isocyanate, hydrogen chloride and non-reacted phosgene, a first liquid supply line for a liquid flow containing at least one quench liquid, and a first liquid discharge line for a liquid flow containing at least part of the quench liquid and part of the isocyanate, a first gas line for transporting a gas flow containing at least hydrogen chloride, evaporated quench liquid and phosgene leading away from the first separating body. The invention is characterized in that at least one addition body for directly introducing at least one cooling fluid for an at least partial condensation and/or absorption of the gas flow that can be guided via the first gas line is associated with the first gas line.

A process for separating a mixture of components is disclosed. A liquid mixture is provided to a separation vessel substantially near a temperature at which a product component freezes. The liquid mixture comprises the product component and a carrier component. The product component and the carrier component are essentially immiscible substantially near the temperature. The liquid mixture is separated into two or more phases, the two or more phases comprising a product component-rich liquid phase and a product component-depleted liquid phase. In this manner, a mixture of components is separated.

A gas clean-up unit includes a first conversion unit configured to perform a first conversion process of converting hydrogen cyanide contained in gas to be treated to ammonia, in presence of a first catalyst and at a first predetermined temperature; a second conversion unit configured to perform a second conversion process of converting carbonyl sulfide in the gas that has been subjected to the first conversion process to hydrogen sulfide, in presence of a second catalyst and at a second predetermined temperature lower than the first predetermined temperature; a cleaning unit configured to perform a cleaning process of bringing the gas into gas-liquid contact with cleaning liquid to remove the ammonia by cleaning; and a desulfurization unit configured to absorb and remove hydrogen sulfide in the gas by bringing the gas that has been subjected to the cleaning process into gas-liquid contact with absorbent.

Systems and methods directed at removing HCN from an FCC process flue gas (and/or generated in the catalyst system reactions themselves) such that the final HCN output is satisfactory; while, in so doing, avoiding undesirable levels of other pollutants contained in that exhaust gas such as NOx. A system includes an assembly having a fluid catalytic cracking (FCC) unit generating a flue gas with HCN and NOx and a catalyst device placed in the flue gas line to remove HCN and NOx. The catalyst device having one or more SCR catalytic articles, as in one free of platinum group metal material (PGM) or a dual functioning SCR catalyst with PGM, or a combination of each. The assembly can be provided with an ammonia supplier and optionally an H2O supplier with associated injection for supply into the flue gas upstream of a catalytic article(s).

Disclosed are metal organic frameworks (MOFs) for adsorbing guest species, methods for the separation of gases using the MOFs, and systems comprising the MOFs. The MOFs comprise a plurality of secondary building units (SBUs), each SBU comprising a repeating unit of one metal cation connected to another metal cation via a first moiety of an organic linker; a layer of connected adjacent SBUs in which a second moiety of the linker in a first SBU is connected to a metal cation of an adjacent SBU, and wherein adjacent layers are connected to each other via linker-to-linker bonding interactions.