New carbon nanomaterials, preferably titanium carbide-derived carbon (CDC) nanoparticles, were embedded into a polyamide film to give CDC/polyamide mixed matrix membranes by the interfacial polymerization reaction of an aliphatic diamine, e.g., piperazine, and an activated aromatic dicarboxylate, e.g., isophthaloyl chloride, supported on a sulfone-containing polymer, e.g., polysulfone (PSF), layer, which is preferably previously prepared by dry/wet phase inversion. The inventive membranes can separate CO.sub.2 (or other gases) from mixtures of CO.sub.2 and further gases, esp. CH.sub.4, based upon the generally selective nanocomposite layer(s) of CDC/polyamide.

New carbon nanomaterials, preferably titanium carbide-derived carbon (CDC) nanoparticles, were embedded into a polyamide film to give CDC/polyamide mixed matrix membranes by the interfacial polymerization reaction of an aliphatic diamine, e.g., piperazine, and an activated aromatic dicarboxylate, e.g., isophthaloyl chloride, supported on a sulfone-containing polymer, e.g., polysulfone (PSF), layer, which is preferably previously prepared by dry/wet phase inversion. The inventive membranes can separate CO.sub.2 (or other gases) from mixtures of CO.sub.2 and further gases, esp. CH.sub.4, based upon the generally selective nanocomposite layer(s) of CDC/polyamide.

A membrane includes a polysulfone-based support, a polydopamine (PDA) layer disposed on a surface of the polysulfone-based support, and a silver/polydopamine (Ag/PDA) composite layer disposed on a surface of the polydopamine layer. The polysulfone-based support has a pore size of up to 600 nanometers (nm). The Ag/PDA composite layer contains core-shell structure particles and spherical particles. The core-shell structure particles have a silver nanoparticle core and a polydopamine shell. The spherical particles are silver-decorated polydopamine particles. The membrane can at least partially separate an Erichrome Black T (EBT) dye from an EBT dye/salt containing mixture by rejecting the EBT dye and allowing the EBT dye/salt containing mixture to pass through the membrane.

New carbon nanomaterials, preferably titanium carbide-derived carbon (CDC) nanoparticles, were embedded into a polyamide film to give CDC/polyamide mixed matrix membranes by the interfacial polymerization reaction of an aliphatic diamine, e.g., piperazine, and an activated aromatic dicarboxylate, e.g., isophthaloyl chloride, supported on a sulfone-containing polymer, e.g., polysulfone (PSF), layer, which is preferably previously prepared by dry/wet phase inversion. The inventive membranes can separate CO.sub.2 (or other gases) from mixtures of CO.sub.2 and further gases, esp. CH.sub.4, based upon the generally selective nanocomposite layer(s) of CDC/polyamide.

The present invention relates to a composite separation film comprising cellulose fiber and silica, a method for manufacturing the separation film, and a secondary battery including the separation film, wherein the separation film has excellent thermal stability, dimensional stability, wettability and electrochemical stability and has a simplified manufacturing process such that the unit cost of production can be reduced.

A method for preparing a polygraphene membrane includes adding graphite and sodium nitrate into sulfuric acid to form a first mixture; adding potassium permanganate solution into the first mixture to form a second mixture; adding hydrogen peroxide solution to the second mixture to form a mixture including soluble manganese ions; filtering the mixture including soluble manganese ions to form an aqueous suspension; centrifuging the aqueous suspension; performing ultrasonication of the suspension to obtain graphene oxide sheets; acylating the graphene oxide sheets to prepare an acylated graphene oxide sheet; and polymerizing the acylated graphene oxide sheets to prepare polygraphene.

Described herein are nanofibers and methods for making nanofibers that include any one or more of (a) a non-homogeneous charge density; (b) a plurality of regions of high charge density; and/or (c) charged nanoparticles or chargeable nanoparticles. In one aspect, the present invention fulfills a need for filtration media that are capable of both high performance (e.g., removal of particle sizes between 0.1 and 0.5 ?m) with a low pressure drop, however the invention is not limited in this regard.

The present invention relates to a technology for manufacturing a nanocomposite membrane comprising a graphene oxide coating layer with a thickness of 1 nm to 50 nm, which is formed on various supports and has nanopores, and a reduced graphene oxide nanocomposite membrane, and applying the membranes to gas separation. The graphene oxide nanocomposite membrane for gas separation of the present invention has excellent gas permeability and selectivity at the same time, and especially, excellent hydrogen gas permeability and hydrogen gas selectivity compared with carbon dioxide, and the reduced graphene oxide nanocomposite membrane has remarkably enhanced hydrogen gas permeability and hydrogen gas selectivity compared with carbon dioxide, and thus the membranes are applicable as a gas separation membrane in an industrial field involving a hydrogen separation process. Furthermore, a graphene oxide nanocomposite membrane for gas separation can be provided, in which strong binding force between a support and a graphene oxide coating layer is induced by modifying surfaces of various supports and thus the graphene oxide coating layer is not easily delaminated.

The present disclosure relates to a porous membrane and a method of manufacturing the same, and more particularly, to a thermally stable porous membrane capable of securing thermal stability and long-term stability of gas separation performance at high temperatures, and a manufacturing method thereof. This invention is related to a porous membrane comprising: a first Zeolitic Imidazolate Fragments (ZIFs) part formed on a surface of a porous support; and a second ZIFs part embedded in the porous support, wherein the second ZIFs part is formed in a state in which it penetrates from an interface between the first ZIFs part and the second ZIFs part to a predetermined depth.

The invention relates to a composition comprising: at least one porous solid additive having a charged surface; an IL; a polymerizable IL; and a cross-linker; wherein the cross-linker wherein the cross-linker has a high affinity to CO.sub.2 over other light gas and comprises at least two polymerizable groups configured to react, in a radical polymerization reaction, with the polymerizable ionic liquid, said polymerizable groups preferably containing double bond.