A carbon dioxide recovery system includes: a heat exchanger that is disposed between a boiler and a desulfurization device, configured to cool exhaust gas flowing from the boiler to the desulfurization device, and configured to heat a heat medium; and a carbon dioxide recovery device that is configured to, when supplied with heat of the heat medium, separate and recover carbon dioxide from an absorber which has absorbed the carbon dioxide.

The invention relates to a gas scrubbing process for purifying crude synthesis gas with methanol as a physical absorption medium, wherein an acid gas comprising at least hydrogen sulfide (H.sub.2S) is produced. The acid gas is produced in a hot regenerator arranged downstream of an absorption apparatus and subsequently separated from gaseous methanol in an acid gas separator by cooling and condensation. The acid gas separator has a condensation region and an absorption region, wherein both regions are separated from one another by a gas-permeable tray. This has the result that impurities such as hydrogen cyanide and/or ammonia outgassing from a first acid gas substream are not reabsorbed in the condensation region of the acid gas separator, thus avoiding an accumulation of impurities in the hot regenerator or other parts of the gas scrubbing plant. The invention further relates to an acid gas separator and to the use of the acid gas separator according to the invention in a process according to the invention.

The disclosure provides an apparatus, as well as associated systems and methods for removing acid gas components from gas streams. The disclosure provides a rotating packed bed (RPB)-based absorber with a non-aqueous liquid solvent contained therein for treatment of the gas streams, wherein the non-aqueous liquid solvent captures acid components from the gas stream. Various advantages, e.g., with respect to spatial considerations and associated expenses can be realized using the apparatus, systems, and methods described herein.

Disclosed are processes, apparatuses, and systems for Direct Air Carbon Capture utilizing waste heat from gas turbines and exhaust air from air cooled heat exchangers, such as in industrial facilities with sources of heat and using fans. The exhaust air from the air cooled heat exchangers may be used to drive one or more fans in one or more Direct Air Carbon Capture units. The waste heat—thus no electricity needed—may be used to regenerate the catalyst(s) in the Direct Air Carbon Capture units.

A carbon processing system comprises an air mover and a multi-stage reactor. The multi-stage reactor processes ambient air and generates carbon dioxide and generates exhausted gas released to ambient air. In operation, air contacts the base solution via the air mover. The air reacts with the base solution thereby generating a base solution having carbon dioxide and generating exhaust (absorption reaction). Next, the exhaust is released from the reactor. Next, heat is applied to the base solution having carbon dioxide thereby generating carbon dioxide and generating a base solution without carbon dioxide (desorption reaction). The base solution without carbon dioxide generated after applying heat is reusable in processing new air. The absorption reaction and desorption reaction are reversible reactions resulting in regeneration of the base solution into its form prior to contact with the air yielding high scalability and less processing volume as required by many conventional carbon processing techniques.

An ambient water condenser system is described having a condensation chamber which at least partially contains or surrounds a fluid reservoir which contains a volume or mass of an aqueous hygroscopic solution for condensing water from ambient air and a distillation process for extracting the water from the solution. The fluid reservoir has a heat source, a lower porous hydrophobic membrane, and an upper porous hydrophobic membrane. The heat source causes the hygroscopic solution near the top of reservoir to have a higher temperature which causes it to have a higher water vapor pressure, whereby the water vapor passing through the upper porous hydrophobic membrane and into the condensation chamber condenses into liquid water.

Devices, systems, and methods for carbon capture optimization in industrial facilities are disclosed herein. An example carbon capture process involves cooling a flue gas stream using at least one gas-to-air heat exchanger disposed upstream of a carbon dioxide (CO2) absorber. Another example carbon capture process involves heating a heat medium for solvent regeneration and CO2 stripping using a fired heater and/or using at least one waste heat recovery unit.

A process for selective capture of CO.sub.2 from gaseous mixture comprising of: (a) spraying a bio-amine cluster; (b) capturing CO.sub.2 through bio-amine cluster; and (c) desorption of CO.sub.2 through solar assisted electro de-amination, wherein the bio-amine cluster is comprises of: an amine cluster comprising of a quaternary Isobutylamine (IB) with amine terminated Poly(L-lactide) as the chelating agent; a cluster stabilizing agent; a cluster micelle stabilizing agent; and a carbonic anhydrase (CA) functionalized matrix in 0.05-0.2 wt % of total wt % of bio-amine cluster and wherein the CA is obtained from a source selected from the group consisting of Bacillus thermoleovorans, Pseudomonas fragi, Bacillus stearothermophilus and Arthrobacter sp. and a process for production of bio-amine cluster.

The invention provides a process for regenerating a liquid absorbent, including: contacting the liquid absorbent with a hydrophobic medium, wherein the liquid absorbent includes at least one amine of Formula (I) ##STR00001##
and degradation product thereof including at least one imine of Formula (II), ##STR00002##
wherein each Ar is independently an aromatic group and each R is independently selected from hydrogen, an organyl group and NH2; and selectively extracting the degradation product into or through the hydrophobic medium.

Disclosed herein are methods of electrochemically enhanced amine-based CO.sub.2 capture and systems for performing the methods of amine-based CO.sub.2 capture. The present methods and systems advantageously may be carried out at ambient temperatures and allow for reusing the amine through multiple cycles.