A method and apparatus are provided for recovering an amine solvent from an acid gas stream. The apparatus includes a water wash recovery column, a nozzle for spraying water wash and an amine nucleation agent into the water wash recovery column and an inlet port for introducing acid gas into the water wash recovery column adjacent the lower end thereof. The method includes the steps of treating the acid gas stream in the water wash recovery column with a counter-current flow of water wash in an amine nucleation agent, discharging treated acid gas from an upper end of the water wash recovery column and collecting water wash, amine nucleation agent and entrained amine solvent from the acid gas stream and a sump at a lower end of the water wash recovery column.

An air-liquid amine contactor for gaseous carbon dioxide extraction includes a manifold and a contactor. The manifold dispenses liquid amine into the contactor in a controlled manner. The liquid amine dispenses as a film that spreads over a plurality of plenum bodies mounted within the manifold. Each of the plurality of plenum bodies includes a plurality of V-shaped channels which increase the overall surface area of the plenum body. The plurality of V-shaped channels includes a first inner wall and a second inner wall positioned at an angle ranging from 24 to 28 degrees to each other. Further, each of the plurality of wedge-inserts includes a first fluid orifice, a second fluid orifice, and an inlet orifice. Each wedge-insert is positioned within a corresponding V-shaped channel. Finally, the contactor is mounted adjacent to the contactor which positions the plurality of V-shaped channels perpendicular to a bottom surface of the manifold.

Primary, secondary (1°,2°) alkylethylenediamine- and alkylpropylenediamine-appended variants of metal-organic framework are provided for CO.sub.2 capture applications. Increasing the size of the alkyl group on the secondary amine enhances the stability to diamine volatilization from the metal sites. Two-step adsorption/desorption profiles are overcome by minimzing steric interactions between adjacent ammonium carbamate chains. For instance, the isoreticularly expanded framework Mg.sub.2(dotpdc) (dotpdc.sup.4−=4,4″-dioxido-[1,1′:4′,1″-terphenyl]-3,3″-dicarboxylate), yields diamine-appended adsorbents displaying a single CO.sub.2 adsorption step. Further, use of the isomeric framework Mg-IRMOF-74-II or Mg.sub.2(pc-dobpdc) (pc-dobpdc.sup.4−=3,3-dioxidobiphenyl-4,4-dicarboxylate, pc=para-carboxylate) also leads to a single CO.sub.2 adsorption step with bulky diamines. By relieving steric interactions between adjacent ammonium carbamate chains, these frameworks enable step-shaped CO.sub.2 adsorption, decreased water co-adsorption, and increased stability to diamine loss. Variants of Mg.sub.2(dotpdc) and Mg.sub.2(pc-dobpdc) functionalized with large diamines such as N-(n-heptyl)ethylenediamine have utility as adsorbents for carbon capture applications.

A metal lattice for a carbon dioxide scrubber includes a metal lattice body defining a plurality of intersecting ligaments, wherein nodes are formed at intersections of the plurality of intersecting ligaments, wherein a node density of the metal lattice body varies.

An apparatus and process for separating and removing CO.sub.2 generated by one or more passengers in the air in the interior of a cabin of a vehicle. Provided are: —a first stream of the air from the interior of the cabin to an interior of a container holding a loose particulate sorbent for CO.sub.2; —a second stream of air depleted in CO.sub.2 from the interior of the container holding the sorbent to an interior of the cabin; —a third stream of the air from exterior of the cabin to the inferior of the container holding the sorbent; and —a fourth stream of air enriched in CO.sub.2 from the interior of the container holding the sorbent to an exterior of the cabin.

Methods and systems for treating an olefin-containing stream are disclosed. The disclosed methods and systems are particularly suitable for treating an off-gas stream in a refining or petrochemical process, such as from a fluid catalytic cracker (FCC), coker, steam cracker, and the like. The stream is treated in an absorber column to reject lighter stream components and to absorb ethylene and/or propylene into a solvent. The solvent is typically isobutane. The enriched solvent stream from the absorber column is fed to an alkylation reactor, which reacts the dissolved olefin with the isobutane solvent to produce an alkylate product.

Electro oxidation membrane evaporator 1 comprises sweep air handler 60; fluid tank 20 defining a fluid container; fluid contactor/separator 30; oxidation cell 40; and scrubber 80. Electro oxidation membrane evaporator 1 may allow higher percent water recovery from wastewater prior to delivering brine to a brine water recovery system and can allow O.sub.2 from air such as cabin air to continuously diffuse into the wastewater as O.sub.2 is consumed to generate oxidants, helping to eliminate the low oxidant environment at the end of the cycle that causes pH to remain high, and low pH prevents precipitates from forming for longer so more water can be evaporated from the wastewater.

The embodiments provide an acidic gas absorbent kept from deterioration, an acidic gas removal method using the absorbent, and an acidic gas removal apparatus using the same. The acidic gas absorbent contains an amine compound and water, and further contains superfine bubble containing inert gas wherein an average diameter of said superfine bubble is 150 nm or less. The acidic gas removal method provided here employs that absorbent. The acidic gas removal apparatus is equipped with a unit for introducing the superfine bubbles into the absorbent.

The methods and systems are disclosed which leverage sulfur abatement resources present at most refineries or other hydrocarbon processing plants, such as natural gas processing plants to capture and treat sulfur-containing byproducts, such as SO.sub.2, generated during the regeneration of spent HDP catalysts. Thus, the disclosed methods and systems allow for converting hazardous waste spent catalyst to a salable product at it source while simultaneously capturing the sulfur oxides removed from the catalyst and converting them to a useful product instead of a resultant waste stream requiring management and/or disposal. Thus, spent sulfur bearing refinery wastes, such as HDP catalyst, can be roasted or regenerated at the refinery site to convert the hazardous sulfur-bearing wastes into one or more salable products.

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.