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.

A transformational energy efficient technology using ionic liquid (IL) to couple with monoethanolamine (MEA) for catalytic CO.sub.2 capture is disclosed. [EMmim.sup.+][NTF.sub.2.sup.−] based catalysts are rationally synthesized and used for CO.sub.2 capture with MEA. A catalytic CO.sub.2 capture mechanism is disclosed according to experimental and computational studies on the [EMmim.sup.+][NTF.sub.2.sup.−] for the reversible CO.sub.2 sorption and desorption.

The present disclosure relates to a porous liquid or a porous liquid enzyme system that includes a high surface area solid and a liquid film substantially covering the high surface area solid. The porous liquid or porous liquid enzyme may be contacted with a fluid that is immiscible with the liquid film such that a liquid-fluid interface is formed. The liquid film may facilitate mass transfer of a substance or substrate across the liquid-fluid interface. The present disclosure also provides methods of performing liquid-based extractions and enzymatic reactions utilizing the porous liquid or porous liquid enzyme of the present disclosure. The present disclosure also provides methods for selecting the components of the porous liquid or a porous liquid enzyme system and methods of self-replenishing the used liquid coating.

A method of enhancing yield and transfer rate of a packed bed in a reactor chamber of a vessel includes steps of applying acoustic energy to the packed bed, measuring impedance of the packed bed deriving a natural resonance frequency of the packed bed from the measured impedance and applying the acoustic energy to the packed bed at the derived natural resonance frequency of the packed bed.

Methods for removing sulfur dioxide from a gas stream are disclosed. A method may include passing a gas stream comprising SO.sub.2 through a gas scrubbing apparatus. A scrubbing liquor comprising hydroxide ions and at least one oxidation catalyst may be flowed into the gas scrubbing apparatus, thereby contacting the gas stream with the scrubbing liquor. In response to the contacting, at least 90 wt. % of the sulfur dioxide may be removed from the gas stream. Concomitant to the contacting, at least some of the sulfur dioxide may react with at least some of the hydroxide ions, thereby forming sulfite ions in the scrubbing liquor. Some of the sulfite ions may be oxidized, via the oxidation catalyst, thereby forming sulfate ions in the scrubbing liquor. A used scrubbing liquor may be discharged from the scrubbing apparatus.

The present invention relates to the use of solid metal materials for catalyzing the hydration of carbon dioxide. It also relates to methods of and apparatus for hydrating carbon dioxide and capturing carbon. The solid metal materials may be nickel nanoparticles. The invention finds particular application in the sequestration of carbon dioxide either at the point of release or from the atmosphere.

The invention relates to a method of selectively removing hydrogen sulfide H.sub.2S from a gaseous effluent comprising at least H.sub.2S and CO.sub.2, wherein a stage of selective absorption of hydrogen sulfide over CO.sub.2 is carried out by contacting said effluent with a solution comprising (a) water and (b) at least the following diamine: 1,2-bis(2-dimethylaminoethoxy)ethane ##STR00001##
and wherein the absorption selectivity is controlled by adding (c) a viscosifying compound to the absorbent solution.

An absorbent for removing carbon dioxide from a fluid stream, comprising an aqueous solution a) of an amine of the general formula (I)

##STR00001##

in which R.sub.1, R.sub.2 and R.sub.3 are each independently selected from C.sub.1-4-alkyl and C.sub.1-4-hydroxyalkyl; each R.sub.4 is independently selected from hydrogen, C.sub.1-4alkyl and C.sub.1-4-hydroxyalkyl; each R.sub.5 is independently selected from hydrogen, C.sub.1-4-alkyl and C.sub.1-4-hydroxyalkyl; X is OH or NH(CR.sub.1R.sub.2R.sub.3); m is 2, 3, 4 or 5; n is 2, 3, 4 or 5; and o is 0 or 1; and b) at least one activator selected from b1) a sterically unhindered primary amine and/or a sterically unhindered secondary amine; and a carboanhydrase. The absorbent allows rapid absorption of carbon dioxide from fluid streams.

The invention relates to a process for removing a target gas from a gas stream rich in the target gas and to an absorbent solution for absorbing a gas, such as carbon dioxide, from a gas stream. The invention involves the use of a photoactive compound that is convertible from a first state to a second state upon irradiation to facilitate removal or collection of a target gas from a gas stream.

A bio-functional air filter medium is provided with a first filter layer that retains particles and at least one bio-functional carrier coated with or having embedded therein antimicrobial material and an anti-allergenic material. An air filter element having the bio-functional air filter medium is also disclosed. The bio-functional air filter medium is adapted to bind and capture allergens and block metabolism of bacteria while filtering air in high flow, low pressure drop residential or HVAC applications.