To provide a PTP blister sheet exhibiting a high adsorption effect over prolonged periods, and a PTP blister pack formed from it. A PTP blister sheet having at least a gas barrier layer and an odor adsorption layer, wherein the odor adsorption layer comprises a heat-sealable resin containing an odor adsorption agent, and the odor adsorption agent is formed by a chemical adsorption agent supported on an inorganic porous body, and a PTP blister pack formed from it.

An apparatus, system, and method for removing impurities from a non-aqueous electrolyte used in an electrochemical cell. The apparatus includes a vessel having one or more chambers with an inlet and an outlet configured to allow the flow of the electrolyte through the one or more chambers; and an inorganic scavenging agent located within the one or more chambers. The inorganic scavenging agent includes one or more types of zeolite particles, at least one type of absorbent filler particles, or a combination of the zeolite and absorbent filler particles. The inorganic scavenging agent absorbs one or more of moisture, free transition metal ions, or hydrogen fluoride (HF) that is present as impurities in the non-aqueous electrolyte.

The present system reduces the cost of carbon capture by reducing the over-temperature needed to strip CO.sub.2 from a liquid or fluid solution. The system includes structures that enhance the rate of CO.sub.2 bubble nucleation.

A modified natural sulfide ore material, a preparation method, and a use thereof are disclosed. A natural sulfide ore and a copper salt are used as raw materials. The natural sulfide ore is modified through mechanical grinding for activation, drying, and the like to synthesize a sulfide ore composite. The copper salt is subjected to a reaction to increase metal sites, produce fine microcrystalline particles, and change the crystal structure, such that active sites can be fully exposed. When contacting mercury in a gas phase and/or a liquid phase, the modified natural sulfide ore material can convert the mercury into a stable compound to realize the immobilization and removal of the mercury, which has advantages such as large mercury adsorption capacity, high adsorption rate, wide application temperature range, low cost, abundant raw material reserves, simple operation, and environmentally-friendly mercury removal products without secondary pollution and shows promising industrial application prospects.

The present invention relates to a flow-through device comprising at least one separation column wherein a first packing component, which comprises particles of alumina and/or silica, and a second packing component, which comprises a powder of one or more hygroscopic salts are provided. The two packing components may be blended or layered in the device, which may comprise a single tube or a plurality of tubes arranged in a plate format, such as the wells of a multiwall plate or tubes in a rack. In addition, the invention relates to a method for removing one or more matrix components, such as pigments, from a biological sample, by passing said sample across a first packing component, which comprises particles of alumina and/or silica, and a second packing component, which comprises a powder of one or more hygroscopic salts.

The present invention relates to a flow-through device comprising at least one separation column wherein a first packing component, which comprises particles of alumina and/or silica, and a second packing component, which comprises a powder of one or more hygroscopic salts are provided. The two packing components may be blended or layered in the device, which may comprise a single tube or a plurality of tubes arranged in a plate format, such as the wells of a multiwall plate or tubes in a rack. In addition, the invention relates to a method for removing one or more matrix components, such as pigments, from a biological sample, by passing said sample across a first packing component, which comprises particles of alumina and/or silica, and a second packing component, which comprises a powder of one or more hygroscopic salts.

A particle comprises an inner part and an outer coating. The inner part comprises CaO and the outer coating comprises hydrophobic nanoparticles of a size less than 1 μm. The particle has an average size of from 1 to 1000 μm. A device adapted to perform an absorption process comprises at least one such particle. A method for manufacturing such a particle comprises mixing CaO with hydrophobic nanoparticles, and mixing with sufficient energy to obtain particles comprising CaO coated with the hydrophobic nanoparticles.

The invention relates to a method for manufacturing a multicapillary packing for an exchange of material including the formation, by a 3D printing method, of a monolith having a porous mass through which a plurality of parallel channels passes, opening on an inlet face and an outlet face of the packing, the 3D printing method being chosen among: selective laser sintering, molten wire deposition, stereolithography, binder spraying and spraying of material, the porous mass being suitable for allowing the diffusion of material to be exchanged between the channels.

The present invention relates to the use of particulate mineral material comprising barite for scavenging heavy metal anions from a liquid medium, wherein the heavy metal anions form water-insoluble barium salts with barium cations of the barite, and wherein the particulate mineral material has a specific surface area of from 0.1 m.sup.2/g to 100 m.sup.2/g, measured using nitrogen sorption and the BET method.

Disclosed herein are processes for treating high-P fluid involving (1) providing a high-P containing stream; (2) chemically treating the high-P stream such that a majority of dissolved P in the stream is transformed into a solid form via sorption of P onto particles placed or precipitated within the stream; and (3) removing the solid form containing P from the chemically treated fine solids stream, such that >about 90% of the total P is removed from the high-P fluid. Also disclosed are systems for treating a high-P stream, the systems involving (1) a chemical treatment station operable to chemically treat and transform equal to or greater than about 90% of dissolved P in a high-P stream into a solid form; and (2) a liquid-solid separator station operable to remove the solid form containing P from the chemically treated high-P stream.