A packing device for mass and heat transfer with a subject fluid includes a housing having opposing ends, and subject fluid openings at each opposing end defining a subject fluid flow path for at least one subject fluid flowing through the packing device. A plurality of mass and heat transfer plates each include an interior heat exchange fluid channel disposed between interior heat transfer surfaces of the mass and heat transfer plates. A heat exchange fluid inlet and fluid outlet can supply and remove heat exchange fluid to the heat exchange fluid channels of the mass and heat transfer plates. The mass and heat transfer plates can be oriented to define there between fluid flow channels for the subject fluid. A method and system for mass and heat transfer with a subject fluid, and a method and system for the removal of CO.sub.2 from a gas stream are disclosed.

A process for treatment of gas mixtures containing acid gas, for the removal of said acid gas from the gas mixtures. The process has (A) an absorption step performed on a gas mixture containing acid gas by means of a solvent system containing at least one liquid absorption solvent for removing from the gas mixture the acid gas contained therein and forming a lean gas mixture, from which at least part of the acid gas have been removed, and an enriched solvent containing the acid gas and (B) a regeneration step, in which the enriched solvent is subjected to a gas/liquid separation step by a flash process to be separated from the absorbed acid gas and to produce an acid gas flow and a regenerated solvent, which is recirculated to the absorption step. The solvent system contains at least one liquid absorption solvent selected from switchable ionic liquids.

A membrane modification method for improving liquid membrane separation of carbon dioxide (CO.sub.2) includes grafting an organic substance containing an amine group on a porous membrane material, and loading water into pore channels of the porous membrane material to prepare a supported liquid membrane for a gas mixture separation experiment of CO.sub.2. In the method, the amine group is introduced through chemical grafting to make the water being alkaline when used as membrane liquid. Compared with an alkaline solution as the membrane liquid, the method can avoid the loss of active alkaline substances and increase the permeation flux of CO.sub.2.

A system of utilizing carbon dioxide comprises a carbon dioxide capturing device for capturing carbon dioxide, an electrochemical reaction device for producing synthetic gas by reducing the carbon dioxide captured by the carbon dioxide capturing device, a hydrogen carrier manufacturing device for manufacturing a hydrogen carrier material by using the synthetic gas produced by the electrochemical reaction device, a dehydrogenation device for producing hydrogen from the hydrogen carrier material manufactured by the hydrogen carrier manufacturing device, and a hydrogen utilization device for utilizing hydrogen produced by the dehydrogenation device, wherein the dehydrogenation device further produces carbon dioxide from the hydrogen carrier material and supplies the carbon dioxide to the carbon dioxide capturing device.

Apparatus and methods for desulfurization and decarbonization of a process gas containing sulfur oxides and CO.sub.2. Ammonia may be used as a desulfurizing and decarbonizing agent. The gas may enter a desulfurization apparatus for desulfurization, and to produce an ammonium sulfate fertilizer. The desulfurized gas may enter a decarbonization apparatus to remove carbon dioxide in the gas, and to produce an ammonium bicarbonate fertilizer. The decarbonized gas may contain free ammonia. The decarbonized gas may be washed with a desulfurization circulating fluid and then with water. The washing fluid may be returned to the desulfurization apparatus for use as an absorbing agent for desulfurization. Acidic desulfurization circulating fluid may be used to wash ammonia, thereby achieving a high ammonia washing efficiency, and a low ammonia slip during the decarbonization process.

Techniques according to the present disclosure include capturing carbon dioxide from a dilute gas source with a CO.sub.2 capture solution to form a carbonate-rich capture solution; separating at least a portion of carbonate from the carbonate-rich capture solution; forming an electrodialysis (ED) feed solution; flowing a water stream and the ED feed solution to a bipolar membrane electrodialysis (BPMED) unit; applying an electric potential to the BPMED unit to form at least two ED product streams including a first ED product stream including a hydroxide; and flowing the first ED product stream to use in the capturing the carbon dioxide from the dilute gas source with the CO.sub.2 capture solution.

A packing for capturing carbon dioxide (CO.sub.2) from a dilute includes at least one panel that includes a mesh material configured to be wetted by a CO.sub.2 capture solution and that defines a gas channel having a first dimension defined along a first direction and a second dimension defined along a second direction different than the first direction, the gas channel configured to receive a flow of CO.sub.2-laden gas from the dilute gas source in the second direction and contact the flow of CO.sub.2-laden gas with the CO.sub.2 capture solution on the mesh material.

According to embodiment, a carbon dioxide capturing system cools a regenerator discharge gas discharged from a regenerator 5 containing carbon dioxide by a cooling unit 8, and then sends the gas to a cleaner 9. The cleaner 9 receives condensed water generated from the regenerator discharge gas cooled by the cooler 9, and a gaseous cooled regenerator discharge gas, and cleans the cooled regenerator discharge gas by a cleaning liquid. The cleaner 9 has a first liquid reservoir 9b configured to store the condensed water, and a second liquid reservoir 9c configured to store the cleaning liquid having cleaned the cooled regenerator discharge gas.

A system configured to capture CO.sub.2 and able to be washed of the captured CO.sub.2 includes a material including an ionic liquid configured to capture CO.sub.2 in response to exposure to a gas comprising CO.sub.2 and to a thermal energy source and an aerogel holding the ionic liquid therein. The system may also include a washing solution configured to wash the captured CO.sub.2 from the material.

An H.sub.2-rich fuel gas stream can be advantageously produced by reforming a hydrocarbon/steam mixture in to produce a reformed stream, followed by cooling the reformed stream in a waste-heat recovery unit to produce a high-pressure steam stream, shifting the cooled reformed stream a first shifted stream, cooling the first shifted stream, shifting the cooled first shifted stream to produce a second shifted stream, cooling the second shifted stream, abating water from the cooled second shifted stream to obtain a crude gas mixture stream comprising H.sub.2 and CO.sub.2, and recovering a CO.sub.2 stream from the crude gas mixture stream. The H.sub.2-rich stream can be advantageously combusted to provide thermal energy needed for residential, office, and/or industrial applications including in the H.sub.2-rich fuel gas production process. The H.sub.2-rich fuel gas production process can be advantageously integrated with an olefins production plant comprising a steam cracker.