Separation media includes a membrane and a plurality of ligands immobilized on the membrane, the plurality of ligands comprising anion-exchange ligands, cation-exchange ligands, thiophilic ligands, hydrophilic ligands, hydrophobic interaction ligands, or a combination thereof. The separation media may be multimodal. The separation media may be configured for separation of target molecules comprising a nucleic acid, nucleotide, nucleoside, nucleobase, or an analogue or derivative thereof, from a reaction mixture. The separation media may be configured for use with organic solvents. A separation device includes the separation media. Materials including a nucleic acid, nucleotide, nucleoside, nucleobase, or an analogue or derivative thereof, may be purified at high speeds using the separation device.

Separation media includes a membrane and a plurality of ligands immobilized on the membrane, the plurality of ligands comprising anion-exchange ligands, cation-exchange ligands, thiophilic ligands, hydrophilic ligands, hydrophobic interaction ligands, or a combination thereof. The separation media may be multimodal. The separation media may be configured for separation of target molecules comprising a nucleic acid, nucleotide, nucleoside, nucleobase, or an analogue or derivative thereof, from a reaction mixture. The separation media may be configured for use with organic solvents. A separation device includes the separation media. Materials including a nucleic acid, nucleotide, nucleoside, nucleobase, or an analogue or derivative thereof, may be purified at high speeds using the separation device.

A low cost, sandwich-structured thin film composite (TFC) anion exchange membrane for redox flow batteries, fuel cells, electrolysis, and other electrochemical reaction applications is described. The sandwich-structured TFC anion exchange membrane comprises a microporous substrate membrane, a first hydrophilic ionomeric polymer coating layer on the surface of the microporous substrate layer, a cross-linked protonated polyamine anion exchange polymer coating layer on top of the first hydrophilic ionomeric polymer coating layer, and a second hydrophilic ionomeric polymer protective layer on top of the cross-linked protonated polyamine anion exchange polymer coating layer. Methods of making the TFC anion exchange membrane comprises a microporous substrate membrane and redox flow battery system incorporating the TFC anion exchange membrane comprises a microporous substrate membrane are also described.

A low cost, sandwich-structured thin film composite (TFC) anion exchange membrane for redox flow batteries, fuel cells, electrolysis, and other electrochemical reaction applications is described. The sandwich-structured TFC anion exchange membrane comprises a microporous substrate membrane, a first hydrophilic ionomeric polymer coating layer on the surface of the microporous substrate layer, a cross-linked protonated polyamine anion exchange polymer coating layer on top of the first hydrophilic ionomeric polymer coating layer, and a second hydrophilic ionomeric polymer protective layer on top of the cross-linked protonated polyamine anion exchange polymer coating layer. Methods of making the TFC anion exchange membrane comprises a microporous substrate membrane and redox flow battery system incorporating the TFC anion exchange membrane comprises a microporous substrate membrane are also described.

An object of the present invention is to provide an ion-exchange membrane for simply and inexpensively separating and purifying exosomes present in a biological sample such as serum. The invention relates to a cellulose-based ion-exchange membrane containing a cellulose-based polymer having at least one hydroxyl group or acetyl group at the 2-, 3-, or 6-position being replaced with a positively charged compound. The invention also relates to a method for purifying exosomes, including subjecting a sample containing exosomes to membrane permeation by using the cellulose-based ion-exchange membrane to allow for adsorption of the exosomes, bringing the membrane into contact with a washing liquid to remove impurities, and bringing the membrane into contact with an eluent to allow for desorption of the exosomes.

An object of the present invention is to provide an ion-exchange membrane for simply and inexpensively separating and purifying exosomes present in a biological sample such as serum. The invention relates to a cellulose-based ion-exchange membrane containing a cellulose-based polymer having at least one hydroxyl group or acetyl group at the 2-, 3-, or 6-position being replaced with a positively charged compound. The invention also relates to a method for purifying exosomes, including subjecting a sample containing exosomes to membrane permeation by using the cellulose-based ion-exchange membrane to allow for adsorption of the exosomes, bringing the membrane into contact with a washing liquid to remove impurities, and bringing the membrane into contact with an eluent to allow for desorption of the exosomes.

The invention encompasses resinate formulations comprising an agricultural active ingredient and an ion exchange resin, wherein the agricultural active ingredient is imbibed upon the ion exchange resin; and methods of treating an agricultural surface. The invention also encompasses methods of manufacturing an agricultural formulation comprising a resinate, comprising: providing an agricultural active ingredient and an ion exchange resin; and mixing the agricultural active ingredient and the ion exchange resin to imbibe the agricultural active ingredient upon the ion exchange resin, thereby forming the resinate.

An endotoxin adsorbent comprising a crystalline cellulose having a nitrogen atom-containing cationic group can sufficiently remove endotoxin from a material containing endotoxin to be removed and containing a substance having a cationic group and can efficiently remove endotoxin also from a highly viscous material. The nitrogen atom-containing cationic group may be typically a functional group derived from a polyvalent amine and/or a quaternary ammonium salt. The crystalline cellulose having a nitrogen atom-containing cationic group may comprise the nitrogen atom-containing cationic group at a content of 0.05 to 3 meq/dry.Math.g in terms of anion exchange capacity.

An endotoxin adsorbent comprising a crystalline cellulose having a nitrogen atom-containing cationic group can sufficiently remove endotoxin from a material containing endotoxin to be removed and containing a substance having a cationic group and can efficiently remove endotoxin also from a highly viscous material. The nitrogen atom-containing cationic group may be typically a functional group derived from a polyvalent amine and/or a quaternary ammonium salt. The crystalline cellulose having a nitrogen atom-containing cationic group may comprise the nitrogen atom-containing cationic group at a content of 0.05 to 3 meq/dry.Math.g in terms of anion exchange capacity.

The embodiments provide a modified filter membrane for separating a crude solution of a biological product and a viral contaminant. The filter membrane has a cellulosed based porous surface, and at least one divalent metal ion bound to the cellulose based porous surface of the filter membrane to form a modified filter membrane cellulose based porous surface, wherein the modified cellulose based porous surface separates the crude solution by retaining a viral contaminant greater than 15 nm in diameter while allowing a biological product smaller than 15 nm in diameter to pass through. The embodiments also provide a method of filtering a crude solution of a biological product and a viral contaminant using a modified filter membrane by adding a divalent metal ion to a filter membrane porous surface to form a modified filter membrane porous surface with a pore size in the range of 1 to 15 nm in size, and filtering the crude solution of the biological product and the viral contaminant through the porous surface of the modified filter membrane, wherein the modified filter membrane retains the viral contaminant on the porous surface while allowing the biological product to pass through.