A method for manufacturing a porous adsorbent coating, including the steps of obtaining a homogeneous mixture including water, mesoporous particles in which the grains have a diameter of less than 800 ?m and a reinforcement, covering all or part of a component to be coated with a layer of homogeneous mixture, and compressing the layer of mixture onto the component to be coated under a pressure of more than 10 bar is disclosed.

A sulfide recovery coating for containers, tanks, pipes, and pipelines, which sulfide recovery coating includes a sulfide capturing agent embedded within a polymer resin matrix. The sulfide capturing agent is a metal oxide and accounts for less than 70 wt % of a total weight a composition for forming the sulfide recovery coating.

Methods and nanocomposites for the adsorptive removal of aromatic hydrocarbons such as benzene, toluene, ethyl benzene and xylene from contaminated water sources and systems are provided. The nanocomposites contain carbon nanotubes and metal oxide nanoparticles such as Al.sub.2O.sub.3, Fe.sub.2O.sub.3 and ZnO impregnated on a surface and/or in pore spaces of the carbon nanotubes. Methods of preparing and characterizing the nanocomposite adsorbents are also provided.

A composite particle having a fluorinated surface and a discontinuous layer of gold nanoparticles disposed on the fluorinated surface, articles that include such particles, and methods of using the particles and the articles for removal of ethylene.

Methods and nanocomposites for the adsorptive removal of aromatic hydrocarbons such as benzene, toluene, ethyl benzene and xylene from contaminated water sources and systems are provided. The nanocomposites contain carbon nanotubes and metal oxide nanoparticles such as Al.sub.2O.sub.3, Fe.sub.2O.sub.3 and ZnO impregnated on a surface and/or in pore spaces of the carbon nanotubes. Methods of preparing and characterizing the nanocomposite adsorbents are also provided.

The present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for their preparation and separations devices containing the chromatographic materials. The chromatographic materials of the invention have controlled porosity and comprise a chromatographic core material and one or more layers of chromatographic surface materials which each independently provide an average pore diameter, an average pore volume, or a specific surface area such that the combined layers form a chromatographic material having a predetermined or desired pattern of porosity from the core material to the outermost surface. The materials are useful for HPLC separations, normal-phase separations, reversed-phase separations, chiral separations, HILIC separations, SFC separations, affinity separations, perfusive separations, partially perfusive separations, and SEC separations.

A method for producing a stationary phase for chromatography including radical copolymerization of a base material having a radically polymerizable functional group and a monomer having a radically polymerizable functional group in the presence of a radical initiator, wherein the radical copolymerization is performed in a heterogeneous system including a phase of the monomer having the radically polymerizable functional group and a phase of a solvent.

A chromatographic media for separating bio-polymers, the chromatographic media having cationic exchange properties and anionic exchange properties, the chromatographic media comprising: (a) non-porous substrate particles including an organic polymer, the substrate particles having a neutral hydrophilic layer at a surface of the non-porous substrate particles, in which the neutral hydrophilic layer is configured to reduce a binding of the bio-polymers directly to the non-porous substrate particles compared to a binding of the bio-polymer to the non-porous substrate particles without the neutral hydrophilic layer; (b) a charged first ion exchange layer bound to the substrate particles on top of the hydrophilic layer, the first ion exchange layer comprising first ion exchange groups; and (c) a charged second ion exchange layer bound to the substrate particles on top of the first ion exchange layer.

The present disclosure relates to a substrate containing passive NO.sub.x adsorption (PNA) materials for treatment of gases, and washcoats for use in preparing such a substrate. Also provided are methods of preparation of the PNA materials, as well as methods of preparation of the substrate containing the PNA materials. More specifically, the present disclosure relates to a coated substrate containing PNA materials for PNA systems, useful in the treatment of exhaust gases. Also disclosed are exhaust treatment systems, and vehicles, such as diesel or gasoline vehicles, particularly light-duty diesel or gasoline vehicles, using catalytic converters and exhaust treatment systems using the coated substrates.

The present invention relates to a method for manufacturing a carbon dioxide absorbent and to the absorbent manufactured by the method. The method comprises: (A) a step of preparing a slurry composition including a carrier composition containing a support, an inorganic binder, and a solvent; (B) a step of preparing solid particles by spray drying the thus-prepared slurry composition; (C) a step of manufacturing a carrier by dry calcining the thus-prepared solid particles; and (D) a step of receiving an amine compound into the pores of the thus-manufactured carrier. According to the absorbent of the present invention, an absorbing reaction and a regenerating reaction at a low temperature range (less than or equal to 100 C. may be conducted, and therefore, the cost for capturing CO.sub.2 in a dry capturing process may be expected to decrease.