The present disclosure relates to hollow core granules, products incorporating the hollow core granules, and methods of making the hollow core granules. The hollow core granules can comprise at least one wall surrounding a cavity that is devoid of any solid or liquid so as to define a hollow core, the at least one wall comprising a plurality of individual particles of at least one wall forming material, the plurality of individual particles sufficiently bound together so that the at least one wall is structurally self-sustaining. The hollow core granules further can include a binder material present in the at least one wall. The hollow core granules can be useful as a standalone material and/or may be useful in preparing a variety of products wherein the hollow core granules may be mixed or otherwise combined with further components. The disclosure further provides methods of making such hollow core granules.

The invention relates to a method to produce a particulate activated carbon material for capturing CO.sub.2 from air,

wherein the particulate activated carbon is impregnated with alkali carbonate salt such as K.sub.2CO.sub.3; and wherein the impregnated particulate activated carbon either has, determined using nitrogen adsorption methods, a pore volume of at least 0.10 cm.sup.3/g for pore sizes of at least 5 nm and a pore volume of at most 0.30 cm.sup.3/g for pore sizes of less than 2 nm or is based on a mixture of different alkali carbonate salts, or has a particular pore surface for pore sizes in the range of 2 nm-50 nm.

The present invention provides an improved sorbent and corresponding device(s) and uses thereof for the capture and stabilization of volatile organic compounds (VOC) or semi-volatile organic compounds (SVOC) from a gaseous atmosphere. The sorbent is capable of rapid and high uptake of one or more compounds and provides quantitative release (recovery) of the compound(s) when exposed to elevated temperature and/or organic solvent. Uses of particular improved grades of mesoporous silica are disclosed.

The present invention provides an improved sorbent and corresponding device(s) and uses thereof for the capture and stabilization of volatile organic compounds (VOC) or semi-volatile organic compounds (SVOC) from a gaseous atmosphere. The sorbent is capable of rapid and high uptake of one or more compounds and provides quantitative release (recovery) of the compound(s) when exposed to elevated temperature and/or organic solvent. Uses of particular improved grades of mesoporous silica are disclosed.

A method for producing porous particles of a cross-linked polymer, and porous particles that can be produced according to the method are disclosed. The porous particles of a crosslinked hydroxy- or amino-group-containing polymer have a relatively low swelling factor. A composite material contains the porous particles dispersed in a continuous aqueous phase. The porous particles, or the composite material, are used for purifying organic molecules and for bonding metals from solutions. A filter cartridge contains the porous particles of a cross-linked polymer or the composite material.

A device and a method for stabilizing wine or other vegetable beverages by removal, in whole or in part, of agents responsible for instability, including proteins and metals, are provided. The device has a tubular container filled internally at least partly with particles of support material covered with a layer of a mesoporous nanostructured adsorbent material comprising titanium oxide, adapted to absorb proteins and metals.

A superabsorbent polymer according to the present invention has excellent initial absorption properties, and thus it may be used in sanitary materials such as diapers, etc., thereby exhibiting excellent performances.

A core-shell type amine-based carbon dioxide adsorbent is described, including a chelating agent resistant to oxygen and sulfur dioxide, to inhibit oxidative decomposition of amine. As a core, a porous support is employed on which an amine compound is immobilized, and, as a shell, an amine layer resistant to inactivity by sulfur dioxide is utilized. Such adsorbent exhibits high oxidation resistance because the chelating agent functions to remove a variety of transition metal impurities catalytically acting on amine oxidation. In addition, the sulfur dioxide-resistant amine layer of the shell selectively adsorbs sulfur dioxide to protect the amine compound of the core and, at the same time, the amine compound of the core selectively adsorbs only carbon dioxide. Sulfur dioxide adsorbed on the shell is readily desorbable therefrom at about 110° C. and thus remarkably improved regeneration stability is obtained during temperature-swing adsorption (TSA) processes in which sulfur dioxide is present.

The present document describes a carbon allotrope-silica composite material comprising a silica microcapsule comprising a silica shell having a thickness of from about 50 nm to about 500 μm, and a plurality of pores, said shell forming a capsule having a diameter from about 0.2 μm to about 1500 μm, and having a density of about 0.001 g/cm3 to about 1.0 g/cm3, wherein said shell comprises from about 0% to about 70% Q3 configuration, and from about 30% to about 100% Q4 configuration, or wherein said shell comprises from about 0% to about 60% T2 configuration and from about 40% to about 100% T3 configuration, or wherein said shell comprises a combination of T and Q configurations thereof, and wherein an exterior surface of said capsule is covered by a functional group; a carbon allotrope attached to said silica microcapsule. Also described is a carbon allotrope-silica composite material comprising a carbon allotrope attached to a silica moiety comprising a silica nanoparticle having a diameter from about 5 nm to about 1000 nm, wherein an exterior surface of said silica nanoparticle is covered by a functional group.

This disclosure describes a process for preparing silica-coated calcium carbonate particles, involving the steps of preparing an aqueous carbonate slurry containing calcium carbonate particles, adding at least one silicate composition to the aqueous carbonate slurry to obtain a carbonate-silicate slurry, lowering a pH of the carbonate-silicate slurry by adding at least one acidic compound to obtain a pH-adjusted slurry containing the silica-coated calcium carbonate particles, and isolating the silica-coated calcium carbonate particles—in which at the adding of the acidic compound is controlled such that a final pH of the pH-adjusted slurry ranges from about 7 to about 10, and the silica-coated calcium carbonate particles include a porous coating having an average pore diameter ranging from 2 nm to 50 nm. This disclosure also describes articles and compositions containing the silica-coated calcium carbonate particles, as well as hollow silica spheres formed from the silica-coated calcium carbonate particles.