The present invention relates to a super-absorbent polymer having excellent properties, both centrifugal retention capacity (CRC) and absorption under pressure (AUP) having been improved by introducing a surface crosslinked layer crosslinked by surface-modified inorganic particles, and to a method for preparing the same. The super-absorbent polymer comprises: a base resin powder containing a crosslinked polymer of water-soluble ethylene-based unsaturated monomers having an at least partially neutralized acidic group; and a surface crosslinked layer formed on the base resin powder, wherein inorganic particles may be chemically bound to the crosslinked polymer contained in the surface crosslinked layer, via an oxygen-containing bond or a nitrogen-containing bond.

This disclosure relates to new filtration systems, granular substrates, granular media and processes that are highly effective for removing suspended oil, particulates and oily particulates from an oil-water mixture. The new filtration media comprises a microporous granular substrate having a combination of specified micro-porosity, hardness and additional characteristics, the substrate being modified by an infused or coated absorption composition. This resulting filtration media displays excellent filtration performance, including outstanding durability and robustness to sustain its excellent performance over a large number of backwash cycles.

Fresh water contamination by heavy metals results from a variety of sources and can be damaging to wildlife, alter landscapes, and impact human health. metals removal form water sources is desirable for improving water quality and preventing adverse effects, but also for metals collection and recycling. Adsorption is a desirable metals extraction technique due to economic feasibility. Nanoscale materials exhibit high surface-area-to-volume ratio that lends to high adsorption and reactivity, making them ideal candidates for adsorptive metals extraction processes. Despite these properties, nanomaterials have elicited safety concerns. The extraordinarily small dimensions of these materials allow them to maneuver biological systems, tissues, and even cells, and combined with high reactivity, this translocation can result in toxic effects. It is therefore imperative that safety of nanomaterials for metals extraction be evaluated in addition to adsorptive properties. The current invention describes nanoparticles composed of magnetite, coated in hydroxyapatite, and functionalized for adsorption with titanium dioxide (TiHAMNPs). This material is safe, provides significant adsorption of metals, and allows efficient collection in magnetic systems.

The present invention relates to a novel polypeptide affinity ligand coupled to solid supports and affinity purification of IgG antibodies. The invention is comprised of (1) the design, generation, and purification of polypeptide ligands, (2) coupling of a polypeptide affinity ligand to a solid support matrix, (3) purification of IgG (polyclonal and monoclonal antibodies), and (4) cleaning and reuse of polypeptide supported solid matrix.

The present disclosure relates to a super absorbent polymer and a preparation method of the same. More specifically, it relates to a super absorbent polymer having a reduced extractable content without deterioration in absorption performance, and to a preparation method of the super absorbent polymer capable of producing the above-described super absorbent polymer by performing a polymerization reaction in the presence of a foaming agent and a carboxylic acid-based additive having a specific structure.

A nitrogen oxide storage material comprising: Mg.sub.1-yAl.sub.2O.sub.4-y, wherein y is a number satisfying 0≤y≤0.2, a noble metal, an oxide of a metal other than the noble metal, and a barium compound, the noble metal, the oxide, and the barium compound being loaded on Mg.sub.1-yAl.sub.2O.sub.4-y. The metal oxide comprises at least one metal oxide selected from zirconium oxide, praseodymium oxide, niobium oxide, and iron oxide.

The present disclosure relates to biodegradable materials and methods of removing using the biodegradable materials to remove phosphorus from water. Additionally, the biodegradable materials may be used as a fertilizer.

Embodiments describe a method of depositing an MOF, including depositing a metal solution onto a substrate, spinning the substrate sufficient to spread the metal solution, depositing an organic ligand solution onto the substrate and spinning the substrate sufficient to spread the organic ligand solution and form a MOF layer.

The invention relates to a method of isolating an immunoglobulin, comprising the steps of: a) providing a separation matrix comprising multimers of immunoglobulin-binding alkali-stabilized Protein A domains covalently coupled to a porous support, b) contacting a liquid sample comprising an immunoglobulin with the separation matrix, c) washing said separation matrix with a washing liquid, d) eluting the immunoglobulin from the separation matrix with an elution liquid, and e) cleaning the separation matrix with a cleaning liquid,
wherein the alkali-stabilized Protein A domains comprise mutants of a parental Fc-binding domain of Staphylococcus Protein A (SpA), as defined by SEQ ID NO: 51 or SEQ ID NO: 52, wherein the amino acid residues at positions 13 and 44 of SEQ ID NO: 51 or 52 are asparagines and wherein at least the asparagine residue at position 3 of SEQ ID NO: 51 or 52 has been mutated to an amino acid selected from the group consisting of glutamic acid, lysine, tyrosine, threonine, phenylalanine, leucine, isoleucine, tryptophan, methionine, valine, alanine, histidine and arginine.

The present disclosure relates to hydrocarbon emission control systems. More specifically, the present disclosure relates to substrates coated with hydrocarbon adsorptive coating compositions and evaporative emission control systems for controlling evaporative emissions of hydrocarbons from motor vehicle engines and fuel systems. The hydrocarbon adsorptive coating compositions include particulate carbon having a BET surface area of at least about 1300 m.sup.2/g, and at least one of (i) a butane affinity of greater than 60% at 5% butane; (ii) a butane affinity of greater than 35% at 0.5% butane; (iii) a micropore volume greater than about 0.2 mug and a mesopore volume greater than about 0.5 ml/g.