A method for regenerating a Cu-BTC material includes: impregnating a Cu-BTC adsorbed with guest molecules in an acidic proton solvent or in a steam environment thereof, and filtering the Cu-BTC material, to obtain a solid; impregnating the solid in a non-acidic organic solvent or a steam environment thereof, and finally filtering, washing and drying the solid, to complete the generation of the Cu-BTC material.

Disclosed in certain embodiments are carbon dioxide sorbents that include porous particles impregnated with an amine compound.

A gas separation system for separating a solvent gas having oxygen atoms from a gas including a hydrocarbon gas, the gas separation system comprising: a gas separation agent; and a control unit that controls at least one among at least the flow rate, pressure, and temperature of the gas, wherein the gas separation agent has at least two organometallic complexes having a three-dimensional lattice structure defined by opposing metal-containing planar ligands, and columnar ligands coordinated between the planar ligands, and the at least two organometallic complexes form an inter-penetrating structure such that one apex portion of a unit cell of one of the organometallic complexes is positioned in a space inside one unit cell of the other organometallic complex.

A carbon dioxide capture structure having a monolithic three-dimensional shape, the structure being porous with interconnected pores which are accessible from an exterior side of the structure. The structure is made of a building material including a first material and a second material. The first material is a sorbent material (e.g. functionalizable for carbon dioxide adsorption). The second material is a binder material including potassium silicate. The present disclosure also relates to a method of making the carbon dioxide structure and a method for removing carbon dioxide from a gas or fluid mixture.

Systems and methods for treating water containing PFAS are disclosed. Adsorption media may be used to remove PFAS from water. An eluent may release PFAS from loaded adsorption media to form a waste stream. An internal combustion engine may be used to mineralize PFAS in the waste stream.

According to one aspect of the present invention, a pressure swing adsorption (PSA) device includes an adsorption tower configured to introduce hydrogen gas and adsorb impurity components in the hydrogen gas by using a pressure swing adsorption (PSA) method, an adsorbent of one layer made of activated carbon or an adsorbent of two layers in which activated carbon and zeolite are stacked being disposed in the adsorption tower, the hydrogen gas containing carbon monoxide (CO) of 0.5 vol % or more and 6.0 vol % or less and methane (CH.sub.4) of 0.4 vol % or more and 10 vol % or less as the impurity components; and a densitometer configured to detect a concentration of CO in the hydrogen gas discharged from the adsorption tower, wherein the impurity components are adsorbed and removed to cause the CO concentration measured by the densitometer to fall below a threshold.

A composition and method for the removal of water from a water-containing hydrocarbon stream, and a method for the production of a metal/water-soluble polymer composite are provided. The composite includes a water-soluble polymer, such as guar gum, and a metal salt, such as aluminum nitrate or copper sulfate. The ratio of the metal salt to the water-soluble polymer is in the range from about 1:1 to about 5:1 by mass. The water-soluble polymer and the metal salt form a crosslinked material. The method for producing the metal/water-soluble polymer composite includes mixing a non-crosslinked water-soluble polymer with a metal salt and water to form a paste. The paste is then dried.

An active catalyst for ammonia synthesis is integrated with a specialty sorbent in a composition or composite, such that the catalyst portion and the sorbent portion are in direct intimate contact, which overcomes the thermodynamic limits for conversion. The sorbent may comprise a metal halide absorbent, zeolite adsorbent, other material absorbents or adsorbents, to capture ammonia as it is produced in intimate or near molecular contact with the catalyst, wherein the composition/composite may be provided in the form of a granular or pellet structure. By removing ammonia essentially as it forms, the forward reaction for producing ammonia can continue nearly unabated such that high net conversion can be achieved in a single pass or cumulative within segmented reactors as operated in series.

The present disclosure relates to a process, a system and a use for removing micropollutants (1) in liquid (2). The process comprises providing liquid (2) to a container (3) adapted to hold a liquid and/or a gas, providing magnetic activated carbon (4), mixing it, separating the magnetic activated carbon (4) using a magnetic separator (5), removing between 1 and 100% of the separated used magnetic activated carbon (4), removing the liquid (2), providing new liquid (2) to the container (3), providing the used magnetic activated carbon (4) to the container (3), adding between 1 and 100% of unused magnetic activated carbon (4), repeating the mixing and separation steps at least one time. The process allows for control of several parameters, such as the flow rate of the liquid, dosage of MAC and ratio used/unused MAC required to remove micropollutants from the liquid.

The present disclosure relates to functionalized carbon-based adsorbents for use in selective removal of paraffin impurities from a light paraffins/olefins mixture, in particular at ambient/normal conditions of temperature and pressure. The carbon-based adsorbent comprises a carbonaceous based material functionalized at least in part on active sites thereof with functional groups configured to selectively adsorb the light paraffins from the mixture, thereby resulting in a purity of at least 99.9% of the light olefins upon separation. As described, the adsorbent may comprise activated carbon functionalized at least in part on active sites thereof with fluorine functional groups. Alternatively, the adsorbent may comprise reduced graphene oxide having at least in part on active sites thereof oxygen groups. Methods for manufacturing the absorbents and use them are also disclosed.