The disclosed pre-concentrator comprises: a base substrate having a trench; a metal layer conformally disposed along the inner surface of the trench; and a three-dimensional porous nanostructure disposed on the metal layer in the trench and having aligned pores connected to each other in three dimensions. The pre-concentrator can improve the concentration performance of a sample and the thermal desorption efficiency of a concentrated sample.

The present disclosure provides advantageous graphene/graphite stabilized composites (e.g., graphene/graphite stabilized emulsion-templated foam composites), and improved methods for fabricating such graphene/graphite stabilized composites. More particularly, the present disclosure provides improved methods for fabricating pristine, graphene/graphite/polymer composite foams derived from emulsions stabilized by graphene/graphite kinetic trapping. In exemplary embodiments, the present disclosure provides that, instead of viewing the insolubility of pristine graphene/graphite as an obstacle to be overcome, it is utilized as a means to create or fabricate water/oil emulsions, with graphene/graphite stabilizing the spheres formed. These emulsions are then the frameworks used to make foam composites that have shown bulk conductivities up to about 2 S/m, as well as compressive moduli up to about 100 MPa and breaking strengths of over 1200 psi, with densities as low as about 0.25 g/cm.sup.3.

Provided are a hydrocarbon adsorbent, an exhaust gas purifying catalyst, and an exhaust gas purifying system, which are capable of adsorbing hydrocarbons, storing the adsorbed hydrocarbons up to a relatively high temperature, and desorbing the adsorbed and stored hydrocarbons at a relatively high temperature.

The hydrocarbon adsorbent contains a multipore zeolite containing, outside the zeolite framework, at least one metal selected from the group consisting of transition metals belonging to Groups 3 to 12 in the periodic table, amphoteric metals belonging to Groups 13 and 14 in the periodic table, alkali metals, and alkaline earth metals; and has a content ratio of the metal of 9% by mass or less relative to the multipore zeolite containing the metal.

Described is a filter-drier core for removing acids and halides that are generated by decomposition of a refrigerant that contains a fluoroiodocarbon, the filter drier core comprising a molded core that includes gamma phase activated alumina and a molecular sieve. The molecular sieve has a pore size between 3-4 angstroms and between 300-00 m.sup.2/g surface area, and/or the alumina is provided in a beaded form with average bead diameter between 0.1-10 mm. An alumina surface area may be between 140-250 m.sup.2/g, and an average pore size may be 6 nm to 16 nm. A percent molecular sieve in the core may be between 0-40%, with the rest of the core being alumina. To increase surface area of the core, the filter-drier core may define a plurality of suitably shaped channels that extend longitudinally through the core, may have fins that extend from a central body, or may be configured as a plurality of rods. A refrigerant system includes a refrigerant circuit through which a refrigerant flows, and a filter-drier unit including the filter-drier core configured for contact with the refrigerant for removing contaminants from the refrigeration system.

Water is separated into deuterium-depleted water having a low deuterium concentration and deuterium-enriched water having a high deuterium concentration easily and at low cost. A method for separating water into deuterium-depleted water and deuterium-enriched water, the method including: adsorbing water vapor on an adsorbent including a pore body having pores 6 while supplying water vapor to and allowing the water vapor to pass through the adsorbent for a predetermined period of time; recovering deuterium-enriched water containing a large amount of heavy water 8 from the water vapor not adsorbed on the adsorbent; and then recovering deuterium-depleted water containing a large amount of light water 7 from the water vapor adsorbed on the adsorbent.

The present disclosure is directed to substrates or topsheets having repeating patterns of apertures for absorbent articles. Each of the repeat units comprises at least three apertures.

The present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for its preparation and separations devices containing the chromatographic material; separations devices, chromatographic columns and kits comprising the same; and methods for the preparation thereof. The chromatographic materials of the invention are chromatographic materials comprising having a narrow particle size distribution.

The invention relates to a stationary phase medium for adsorption chromatography, which is in form of porous particles suitable for being packed into a chromatographic column. The porous particles are made of cross-linked polymeric material and formed with interconnected macropores to constitute a porous network, through which a mobile phase fluid may flow in a convective manner. The porous particles are substantially free of diffusive pores and, thus, the mass transfer through the porous network is governed by convection alone. The porous particles are fabricated to have irregular granular configurations with rough outer surfaces, so that the convective flow between the porous particles will not be impeded during chromatography process.

The present disclosure relates to a preparation method for a super absorbent polymer sheet and a super absorbent polymer sheet prepared therefrom. According to the preparation method of the present disclosure, a porous super absorbent polymer sheet can be prepared by a simplified process.

The present invention relates to an organic polymer adsorbent, an organic polymer adsorbent composition, and a method for preparing an organic polymer adsorbent and, more specifically, to an organic polymer adsorbent to be used for a ventilation device such as a desiccant dehumidifier. According to the present invention, an adsorbent material is changed to an organic polymer adsorbent such that the mechanical stability and durability of the material itself can be ensured, and the specific surface area of interconnected inner pores and adsorbents and the size of formed pores can be controlled since toluene is contained as a pore generator of the adsorbent. Therefore, the adsorbent of the present invention has superior adsorption performance over that of other conventional organic polymer adsorbents containing a salt-type carboxyl group and has remarkably improved desorption performance, and thus has an effect of very remarkable energy efficiency.