Provided is a carbon dioxide recovery system including: an absorption tower; a regeneration tower that takes in an absorbing solution that has absorbed carbon dioxide at the absorption tower, and separates the carbon dioxide from the absorbing solution using regenerated steam to regenerate the absorbing solution; first supply piping that supplies the absorbing solution regenerated in the regeneration tower to the absorption tower; a reclaimer that takes in part of the absorbing solution regenerated in the regeneration tower to remove degraded material and supplies the absorbing solution from which the degraded material has been removed to the regeneration tower or the first supply piping; an in-line viscometer that measures a viscosity of the absorbing solution flowing through the first supply piping; and a controller that controls an amount of the absorbing solution processed by the reclaimer based on the viscosity measured by the in-line viscometer.

A method of purifying air via a pre-purification unit (PPU) of an air separation unit (ASU) system having a pre-PPU chiller that is upstream of the PPU to cool compressed air before the compressed air is fed to the PPU can include passing air through an adsorber of the PPU to pass the air through a bed of adsorbent material within a vessel of the adsorber. In response to the pre-PPU chiller being determined to have an issue resulting in the pre-PPU chiller being tripped or requiring the pre-PPU chiller to be taken off-line, continuing to operate the ASU system at a full capacity even though nitrous oxide (N2O) within the air output from the PPU exceeds a first pre-selected threshold and is below a second pre-selected threshold associated with carbon dioxide (CO2) breakthrough. An ASU and a PPU can be designed to implement an embodiment of the method.

Systems and methods are provided for separation of CO.sub.2 from dilute source streams. The systems and methods for the separation can include use of contactors that correspond radial flow adsorbent modules that can allow for efficient contact of CO.sub.2-containing gas with adsorbent beds while also facilitating use of heat transfer fluids in the vicinity of the adsorbent beds to reduce or minimize temperature variations. In particular, the radial flow adsorbent beds can be alternated with regions of axial flow heat transfer conduits to provide thermal management. The radial flow structure for the adsorbent beds combined with axial flow conduits for heat transfer fluids can allow for sufficient temperature control to either a) reduce or minimize temperature variations within the adsorbent beds or b) facilitate performing the separation using temperature as a swing variable for controlling the working capacity of the adsorbent.

A carbon dioxide recovery system that recovers carbon dioxide from a hybrid vehicle traveling in a CO.sub.2 recovery area including a CO.sub.2 recovery road in which a stationary CO.sub.2 recovery device collecting and recovering carbon dioxide from the atmosphere is provided acquires a residual charging capacity of the battery and position information of the hybrid vehicle and guides the hybrid vehicle such that the hybrid vehicle travels on the CO.sub.2 recovery road using a notification device when the residual charging capacity is equal to or less than a predetermined SOC threshold value while the hybrid vehicle is traveling in the CO.sub.2 recovery area.

A carbon dioxide (CO.sub.2) capture and utilization system captures CO.sub.2 from flue gas and utilizes the same to enhance algae or cyanobacteria growth. The system generally comprises a CO.sub.2 capture unit and a utilization unit that is in fluid communication with the CO.sub.2 capture unit. The CO.sub.2 capture unit includes a membrane CO.sub.2 absorber that captures CO.sub.2 from incoming flue gas to produce a CO.sub.2-rich solvent. The utilization unit processes the CO.sub.2-rich solvent to produce a product stream that includes CO.sub.2 and NH.sub.3 in a predetermined CO.sub.2:NH.sub.3 ratio. The product stream is delivered to a cultivation subsystem of the utilization of the unit including one or more species of algae or cyanobacteria. A method for capturing and utilizing CO.sub.2 is also provided herein.

The disclosure provides a method and a system for processing concrete granulate for subsequent recycling of the concrete granulate. In the method, a container of the system is filled with concrete granulate, said container being gas-tight at least in some regions. Subsequently, gas comprising CO2 is fed, continuously or noncontinously, according to a level of CO2 absorption by the concrete granulate in the container, said level being determined by means of at least one sensor. After a predefined CO2 saturation of the concrete granulate has been detected, the concrete granulate, which have been enriched with CO2, are removed.

The present invention provides highly permeable and porous polybenzimidazole membranes, methods of making them, and their application as a high-performance membrane support for gas separation composite membranes. The polybenzimidazole membranes are bonded to a fabric substrate.

Generating methane by adding hydrogen to CO.sub.2 in exhaust gas discharged a from cement production facility or CO.sub.2 that is separated and recovered from the exhaust gas, and using the methane as an alternative fuel to fossil fuel such as coal, petroleum, natural gas and the like, by methanation of CO.sub.2 in the exhaust gas from the cement production facility that includes exhaust gas originated from lime stone not from the fossil oil and effectively utilizing it, it is possible to reduce usage of the fossil fuel, suppress CO.sub.2 originated from energy, and improve an effect of reducing greenhouse gas.

A solvent system for the removal of acid gases from mixed gas streams is provided. Also provided is a process for removing acid gases from mixed gas streams using the disclosed solvent systems. The solvent systems may be utilized within a gas processing system.

Capture of hydrogen sulfide from a gas mixture may be accomplished using an aqueous solution comprising an amine. Certain sterically hindered amines may selectively form a reaction product with hydrogen sulfide under kinetically controlled contacting conditions and afford a light phase and a heavy phase above a critical solution temperature, wherein the hydrogen sulfide may be present in either phase. Upon separation of the light phase from the heavy phase, processing of one of the phases may take place to remove hydrogen sulfide therefrom. Recycling of the amine to an absorber tower may then take place to promote capture of additional hydrogen sulfide.