The present invention describes the process of preparing ceramics for the absorption of ACIDIC gases, which worsen the greenhouse effect, that are released in combustion systems, or that are present in closed environments. In relation to carbon dioxide, principal target of the present invention, the process of absorption, transport, processing and transformation of the gas into other products is described. The process uses ceramic materials prepared through the solid mixture of one or more metallic oxides, with one or more binding agents and an expanding agent. The product generated can be processed and the absorbent system regenerated. The carbon dioxide obtained in the processing can be used as analytic or commercial carbonic gas, various carbamates and ammonium carbonate.

The invention is directed to utilization of a series of cross-linked 1,4-benzenediamine-co-alkyldiamine polymers and the use of the polymers to remove mercury from a hydrocarbon in fluid form.

Methods and compositions are provided for treatment of an apatite-based resin from which retained solutes have been eluted by an elution buffer that contains an alkali metal salt with solutions of calcium ion, phosphate ion, and hydroxide separately from any sample loading and elution buffers. The treatment solutions restore the resin, reversing the deterioration that is caused by the alkali metal salt in the elution buffer.

Disclosed are magnetic nanoparticles and methods of using magnetic nanoparticles for selectively removing biologics, small molecules, analytes, ions, or other molecules of interest from liquids.

The disclosure relates to systems and methods for generating a brine solution using a salt cartridge for recharging zirconium phosphate in a reusable sorbent module. The salt cartridge can include an inlet and an outlet on opposite sides. Water can be pumped through the salt cartridge to dissolve the salts in the salt cartridge and the resulting solution can be collected as a brine solution for use in recharging the zirconium phosphate.

Hydrogel-based sorbents and methods for their use in collecting, concentrating, and removing environmental per- and poly-fluoroalkyl substances. In one aspect, the invention provides hydrogel-based sorbents that are effective for collecting, concentrating, and removing PFASs from an environment in which the sorbent is placed; an environment in which the sorbent is in contact with (e.g., liquid communication).

An ammonia chemical species desorption process desorbs ammonia chemical species adsorbed onto a Prussian blue derivative more simply at lower cost under milder conditions as compared with using an aqueous solution of a salt or strong acid, and only water. This ammonia chemical species desorption process includes an ammonia chemical desorption step of bringing carbon dioxide and water into contact with a Prussian blue derivative represented by the following general formula (1), thereby desorbing an ammonia chemical species.

A.sub.xM[M′(CN).sub.6].sub.y.zH.sub.2O  (1)

where x is 0 to 3, y is 0.1 to 1.5, z is 0 to 6, A is at least one cation of hydrogen, ammonium, an alkaline metal, and an alkaline earth metal, and M and M′ are each independently at least one cation of at least one of atoms having atomic numbers 3 to 83 except for ammonium, an alkali metal, and an alkaline earth metal.

A method of using a nanoporous carbon material for adsorption of one or more PAH and diesel fuel from an aqueous solution is described. The aqueous solution may comprise the one or more PAH at a concentration of 0.1 mg/L-1 g/L, and the diesel fuel at a concentration of 0.1-5 g/L. The nanoporous carbon material may adsorb at least 96 wt % of one or more PAH within 10 minutes. The nanoporous carbon material may be obtained by contacting a carbonized asphalt with a base.

An adsorbent includes a porous substrate and a carboxylic acid dimer loaded onto the porous substrate. The carboxylic acid dimer is loaded on the surface or in the plurality of holes of the porous substrate. The average pore size of the porous substrate is not smaller than 2 nm. The carboxylic acid dimer is loaded onto the porous substrate by at least one of the following manners: a) the carboxylic acid dimer is loaded onto the porous substrate through a Si—OH bond; b) the carboxylic acid dimer is loaded onto the porous substrate through the exchange between a carboxyl group and chlorine; c) the carboxylic acid dimer is loaded onto the porous substrate through the exchange between a carboxyl group and a hydroxyl group; and d) the carboxylic acid dimer is loaded onto the porous substrate through the coordination of a carboxyl group and aluminum or silicon.

A method of recycling superabsorbent polymers derived from a used absorbent article, the method including: treating the superabsorbent polymers with ozone water after inactivation; reactivating, with an alkaline aqueous solution, the superabsorbent polymers treated with the ozone water; and adding hydrophilic fine particles to the superabsorbent polymers reactivated with the alkaline aqueous solution and then drying the superabsorbent polymers.