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.

A Nitrogen Oxide (NOx) sorbent material of the present invention includes a multi-metallic oxide that includes one or more alkali or alkaline earth metal, one or more 3d transition metal, and one or more rare earth element. The NOx sorbent material is configured to adsorb and absorb NOx below a low temperature and to release the adsorbed or absorbed NOx at temperature at or above the low temperature. In some embodiments, a manganese catalyst is deposited on a high surface area carrier. The manganese catalyst takes the form of an alkali/metal promotor and an Mn-based compound. In general, the NOx sorbent material contains about one percent to about fifty percent by weight of alkali/alkaline earth metal manganese catalyst based on the total weight of the catalyst.

A hydrophobic adsorbent composition and process for removal of mercury from a gas phase fluid near the water and/or hydrocarbon dew point is disclosed herein.

Provided is an adsorbent for capturing carbon dioxide and a method for manufacturing same, and more particularly, to an adsorbent for capturing carbon dioxide, including a magnesium oxide/titanium dioxide composite having wide surface area, large pore volume and good CO.sub.2 adsorption performance, and a method for manufacturing same. According to the present invention, a novel MgO based composite metal oxide which may stably adsorb CO.sub.2 at a low temperature such as room temperature is provided. The adsorbent for capturing carbon dioxide, including a magnesium oxide/titanium dioxide composite has good thermal stability, and controls basic sites easily, and is used in various fields for capturing carbon dioxide. In addition, by controlling the molar ratio of the metal ions of the magnesium oxide/titanium dioxide composite and controlling morphology, an adsorbent for capturing carbon dioxide having large surface area and pore volume and strong basic sites may be provided.

An oxygen absorbent composition which comprises a polyester oligomer containing a constitutional unit derived from a tetralin ring-containing carboxylic acid and a diol, wherein the polyester oligomer has a number average molecular weight of 500 to 10000, and a transition metal catalyst comprising at least one transition metal selected from the group consisting of manganese, iron, cobalt, nickel and copper.

A sorbent structure that includes a continuous body in the form of a flow-through substrate comprised of at least one cell defined by at least one porous wall. The continuous body comprises a sorbent material carbon substantially dispersed within the body. Further, the temperature of the sorbent structure can be controlled by conduction of an electrical current through the body.

A gas adsorbing material particle includes an additive material particle having a moisture adsorption property; and a layer of a gas adsorbing metal disposed on a surface of the additive material particle, wherein the gas adsorbing metal is inactivated by moisture and adsorbs a target gas, wherein an average thickness of the layer of the metal is less than or equal to about 37 micrometers.

Some embodiments of the present disclosure relate to a device comprising a sorbent polymer composite and at least one phosphonium halide. In some embodiments, the device is configured to treat a flue gas stream. In some embodiments, the flue gas stream comprises oxygen, water vapor, at least one SOx compound, and mercury vapor. Some embodiments of the present disclosure relate to a method comprising treating the flue gas stream by: passing the flue gas stream over the device, reacting the oxygen and water vapor of the flue gas stream with the at least one SOx compound on the sorbent polymer composite, so as to form sulfuric acid, and reacting the mercury vapor with the at least one phosphonium halide, so as to fix molecules of the mercuiy vapor to the sorbent polymer composite.

This disclosure relates to the adsorption and separation of carbon dioxide in a feed stream (e.g., natural gas) using zeolite ITQ-55 as the adsorbent. A process is disclosed for removing impurities such as carbon dioxide and nitrogen while producing a hydrocarbon product. The process involves passing a feed stream through a bed of an adsorbent comprising zeolite ITQ-55 to adsorb carbon dioxide from the feed stream, thereby producing a product stream depleted in carbon dioxide. The zeolite ITQ-55 has a mean crystal particle size within the range of from about 0.1 microns to about 100 microns. The feed stream is exposed to the zeolite ITQ-55 at effective conditions for performing a kinetic separation, in which the kinetic separation exhibits greater kinetic selectivity for carbon dioxide than for methane or nitrogen. The system and method of this disclosure are particularly suitable for use with feed streams in excess of 10 MMSCFD utilizing rapid cycle PSA operations by tuning crystals size.

Carbide-derived carbons are provided that have high dynamic loading capacity for high vapor pressure gasses such as H.sub.2S, SO.sub.2, or NH.sub.3. The carbide-derived carbons can have a plurality of metal chloride or metallic nanoparticles entrapped therein. Carbide-derived carbons are provided by extracting a metal from a metal carbide by chlorination of the metal carbide to produce a porous carbon framework having residual metal chloride nanoparticles incorporated therein, and annealing the porous carbon framework with H.sub.2 to remove residual chloride by reducing the metal chloride nanoparticles to produce the metallic nanoparticles entrapped within the porous carbon framework. The metals can include Fe, Co, Mo, or a combination thereof. The carbide-derived carbons are provided with an ammonia dynamic loading capacity of 6.9 mmol g.sup.−1 to 10 mmol g.sup.−1 at a relative humidity of 0% RH to 75% RH.