A process for the hydrophobization of a porous silica based compound involves the steps of providing a composition (I) containing a porous silica based compound, treating the composition (I) with a composition (II) containing hexamethyldisiloxane or its hydrolyzed form, and removing the treated silica based compound. The porous silica based compound obtained by the process is useful. A porous silica based compound obtained or obtainable by the process can be used for medical and pharmaceutical applications, as adsorbents, for cosmetic applications, as an additive for food, as a catalyst support, for the preparation of sensors, or for thermal insulation.

A filtering and adsorbent sampling and enrichment system comprising a stationary phase consisting of a felt of activated carbon fibres with a micro-meso porous conformation and specific surface area of about 1500 m2/g and sampling and/or enrichment standards, confined within a closed casing, is described, as well as the method for obtaining it and the relative process for the analysis of organic and inorganic analytes that uses said system.

A method of separating analytes in a liquid sample includes flowing the liquid sample through a chromatography column configured for use in liquid chromatography. The chromatography column contains a composition that includes a solid support having an exterior surface, a ligand, and a linker. The ligand includes a polyhedral oligomeric silsesquioxane moiety. The linker is covalently bound to both the polyhedral oligomeric silsesquioxane moiety and the exterior surface of the solid support.

Carbon dioxide and VOC sorbents that include a porous support impregnated with an amine compound are provided. The sorbents include a gas-adsorbing material coated onto the porous support. The gas-adsorbing material includes a polyamine which is produced using a process that is free of formaldehyde as a reaction product and/or a reactant.

The invention relates to inorganic particles which are covalently bonded to first polymer chains made up of at least one polymer carrying proton exchange groups, optionally in the form of salts, and bonded to second polymer chains made up of at least one fluorinated polymer that does not carry any proton exchange groups, the second chains being bonded to the particles via organic spacer groups, or the second chains being bonded to first chains via organic spacer groups, or some of the second chains being bonded to the particles via organic spacer groups while the remaining second chains are bonded to first chains via organic spacer groups.

The present disclosure relates to a carbon-based porous material microscopically exhibiting a three-dimensional cross-linked net-like hierarchical pore structures with micropores nested in mesopores that are in turn nested in macropores. Such material provides for accelerated adsorption and desorption rates and lower desorption temperatures for recovery of organic gas molecules.

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 present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for their preparation and separations devices containing the chromatographic materials. The preparation of the inorganic/organic hybrid materials of the invention wherein a surrounding material is condensed on a superficially porous hybrid core material will allow for families of different hybrid packing materials to be prepared from a single core hybrid material. Differences in hydrophobicity, ion-exchange capacity, chemical stability, surface charge or silanol activity of the surrounding material may be used for unique chromatographic separations of small molecules, carbohydrates, antibodies, whole proteins, peptides, and/or DNA.

A method of increasing hydrothermal stability of an adsorbent comprising a small pore cationic zeolite in a swing adsorption process is disclosed. The method comprises the steps of coating the zeolite with a silylation agent to result in a silylated zeolite; and performing the swing adsorption process. The swing adsorption process comprises contacting the silylated zeolite with feed stream comprising water. The swing adsorption process may comprise removing CO.sub.2 from a feed stream comprising CO.sub.2 and water.

The present disclosure is directed to methods for performing size exclusion chromatography. Embodiments of the present disclosure feature methods for improving separations of proteinaceous analytes in size exclusion chromatography, for example, by using low concentrations of amino acids or derivatives thereof in the mobile phase.