An article that can be used for biomaterial capture comprises (a) a porous substrate; and (b) borne on the porous substrate, a polymer comprising interpolymerized units of at least one monomer consisting of (1) at least one monovalent ethylenically unsaturated group, (2) at least one monovalent ligand functional group selected from acidic groups, basic groups other than guanidino, and salts thereof, and (3) a multivalent spacer group that is directly bonded to the monovalent groups so as to link at least one ethylenically unsaturated group and at least one ligand functional group by a chain of at least six catenated atoms.

Presented is a chemical formaldehyde filter comprising a filter substrate having a porous structure; the filter substrate comprising a mixture of a formaldehyde absorbent and a porous framework material. Further, a method for fabricating such a filter is described.

A composition of matter wherein the composition comprises a siliceous substrate having silanols on the surface and a polymer selected from the group consisting essentially of a water soluble polymer, a water soluble copolymer, an alcohol soluble polymer, an alcohol soluble copolymer, and combinations of such polymers, wherein the polymer is chemically bonded to the siliceous substrate by a silane linking material having the general formula

O.sub.3/2SiQY

that is derived from an alkoxy-functional silane having the general formula

(RO).sub.3SiQX

and processes for preparing the crosslinked polymer that is chemically bonded to the surface of the siliceous substrate.

The present invention provides composite material having a porous graphene-based foam matrix and comprising porous inorganic micro-particles and metal oxide nano-particles distributed throughout the foam matrix.

The invention relates to the use of a citrate solution for affinity-chromatographic removal of C-reactive protein (CRP) from biological fluids, wherein the CRP is affinity-chromatographically removed using (Ca.sup.2+-dependent) binding of CRP to a column material functionalized with ?-phosphonooxyalkyl ammonium groups and/or with ?-ammoniumalkoxy-hydroxy-phosphoryloxy groups.

An article that can be used for biomaterial capture comprises (a) a porous substrate; and (b) borne on the porous substrate, a polymer comprising interpolymerized units of at least one monomer consisting of (1) at least one monovalent ethylenically unsaturated group, (2) at least one monovalent ligand functional group selected from acidic groups, basic groups other than guanidino, and salts thereof, and (3) a multivalent spacer group that is directly bonded to the monovalent groups so as to link at least one ethylenically unsaturated group and at least one ligand functional group by a chain of at least six catenated atoms.

The present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for their preparation and separations devices containing the chromatographic materials. The chromatographic materials of the invention have controlled porosity and comprise a chromatographic core material and one or more layers of chromatographic surface materials which each independently provide an average pore diameter, an average pore volume, or a specific surface area such that the combined layers form a chromatographic material having a predetermined or desired pattern of porosity from the core material to the outermost surface. The materials are useful for HPLC separations, normal-phase separations, reversed-phase separations, chiral separations, HILIC separations, SFC separations, affinity separations, perfusive separations, partially perfusive separations, and SEC separations.

Open tubular capillary columns for liquid and ion chromatography, based upon an ionically impermeable polyolefin capillary having a bore with a sulfonate-group- or amine-group-functionalized internal surface. The capillary columns may include a coating of ion exchanging nanoparticles electrostatically bound to the functionalized internal surface. The capillary columns may be made by exposing the interior surface to a sulfonating reagent comprising chlorosulfonic acid (ClSO.sub.3H), preferably from 85 wt % to 95 wt % chlorosulfonic acid at a process temperature of 20 to 25 C. The interior surface may be subsequently exposed to an asymmetrical diamine to form a sulfonic mid-linkage to the diamine, i.e., to form a sulfonamide-linked, amine-group-functionalized internal surface. The coating may be provided by subsequently exposing the interior surface to an aqueous suspension of ion exchanging nanoparticles to electrostatically bond the ion exchanging nanoparticles to the functionalized internal surface.

The biosynthesized magnetic metal nanoparticles for oil spill remediation are magnetic nanoparticles capped with an extract of Anthemis pseudocotula. The magnetic nanoparticles are formed by co-precipitation of ferric chloride hexahydrate and ferrous chloride tetrahydrate in an ethanol solution of the extract with the dropwise addition of ammonium hydroxide to raise the pH to between 8 and 11. The extract may be an extract of the aerial parts of Anthemis pseudocotula in a low polar extraction solvent, such as an n-alkane solvent or mono-di-, or trichloromethane. The extract is hydrophobic, improving dispersion of the magnetic nanoparticles in oil spills in seawater, resulting in 90% removal of oil for a 1:10 ratio of nanoparticles:oil by weight.

Methods for removing a target anion entity, such as a phosphate ion, from fluids by treating the fluid with a substrate containing an immobilized rare earth, the substrate being either a first loaded substrate including a first immobilized cationic rare earth, the first loaded substrate being formed by precipitating a rare earth in a clay such that the rare earth is fixed inside a porous structure of the clay and/or fixed on the surface of the clay; or a second loaded substrate comprising a second immobilized cationic rare earth that is bonded to the second loaded substrate via a chelating ligand.