Provided is a membrane distillation system capable of real-time monitoring on membrane scaling, which includes: a raw water storage tank configured to store various kinds of fluid; a membrane distillation water treatment unit configured to receive raw water stored in the raw water storage tank to generate pure water, the membrane distillation water treatment unit having an inlet water chamber into which an inlet water flows from the raw water storage tank, a membrane for separating the inlet water in the inlet water chamber into a steam and a concentrated water, and a treated water chamber for receiving the steam separated by the membrane and concentrating the steam; and a membrane wetting detection unit disposed opposite to the membrane to detect a membrane wetting phenomenon and a membrane wetting location of the membrane by measuring a light passing through the membrane in real time.

Provided is a membrane distillation system capable of real-time monitoring on membrane scaling, which includes: a raw water storage tank configured to store various kinds of fluid; a membrane distillation water treatment unit configured to receive raw water stored in the raw water storage tank to generate pure water, the membrane distillation water treatment unit having an inlet water chamber into which an inlet water flows from the raw water storage tank, a membrane for separating the inlet water in the inlet water chamber into a steam and a concentrated water, and a treated water chamber for receiving the steam separated by the membrane and concentrating the steam; and a membrane wetting detection unit disposed opposite to the membrane to detect a membrane wetting phenomenon and a membrane wetting location of the membrane by measuring a light passing through the membrane in real time.

Synthesis, fabrication, and application of nanocomposite polymers in different form (as membrane/filter coatings, as beads, or as porous sponges) for the removal of microorganisms, heavy metals, organic, and inorganic chemicals from different contaminated water sources.

A solution is to produce an acid gas separation composite membrane provided with an acid gas separation facilitated membrane on a porous support, including; arranging of a coating liquid for acid gas separation formed through dispersing or dissolving into water a polyvinyl acetal compound formed through crosslinking, by an acetal bond, block copolymers formed through bonding of a polymer block formed of polyvinyl alcohol and a polymer block formed of polyacrylate through a linking group, an acid gas carrier and at least one kind of anion other than hydroxide ion, carboxyl ion, carbonate ion and bicarbonate ion, and coating of the coating liquid for acid gas separation onto a hydrophobic surface of the porous support having hydrophobicity at least on one surface to form the acid gas separation facilitated transport membrane thereon.

A forward osmosis membrane for seawater desalination and a method for preparing the same. The forward osmosis membrane has a composite membrane structure including a nonwoven fabric layer; a hydrophilic polymer layer; and a polyamide layer. The hydrophilic polymer layer formed on the nonwoven fabric layer facilitates an inflow of water from the feed water to the draw solution to enhance flux and realize high water permeability in the direction of osmosis. The polyamide layer not only secures contamination resistance and chemical resistance but also minimizes the back diffusion of salts of the draw solution in the direction of reverse osmosis. Hence, the forward osmosis membrane of the present invention is greatly useful for desalination of high-concentration seawater.

The present invention relates to a CO.sub.2 selective gas separation membrane and a method for preparing the gas separation membrane and the use thereof. The CO.sub.2 selective gas separation membrane comprises a gas permeable or porous support layer; and at least one gas permeable polymer layer, which is surface modified with polymer chains having CO.sub.2 philic groups, wherein the gas permeable polymer layer has a spatially controlled distribution of the CO.sub.2 philic groups on the surface thereof. The method of preparing the CO.sub.2 selective gas separation membrane, comprises the steps of: depositing at least one gas permeable polymer layer on a porous or gas permeable support layer to form a dense membrane, and surface modifying the dense membrane with polymer chains having CO.sub.2 philic groups, to obtain spatially controlled distribution of the CO.sub.2 philic groups on the surface thereof.

Disclosed are copolymers, comprising a plurality of zwitterionic repeat units, and a plurality of hydrophobic repeat units, wherein the hydrophobic repeat units each independently comprises a cross-linkable moiety; the cross-linked copolymer network, comprising such copolymer; as well as thin film composite membrane comprising such cross-linked copolymer network.

Provided is a facilitated CO.sub.2 transport membrane having improved CO.sub.2 permeance and improved CO.sub.2 selective permeability. The facilitated CO.sub.2 transport membrane includes a separation-functional membrane comprising a hydrophilic polymer gel membrane which contains a CO.sub.2 carrier and a CO.sub.2 hydration catalyst, wherein the hydrophilic polymer is a copolymer including a first structural unit derived from an acrylic acid cesium salt or an acrylic acid rubidium salt and a second structural unit derived from vinyl alcohol. More preferably, the CO.sub.2 hydration catalyst has catalytic activity at a temperature of 100° C. or higher.

Provided is a facilitated CO.sub.2 transport membrane having improved CO.sub.2 permeance and improved CO.sub.2 selective permeability. The facilitated CO.sub.2 transport membrane includes a separation-functional membrane comprising a hydrophilic polymer gel membrane which contains a CO.sub.2 carrier and a CO.sub.2 hydration catalyst, wherein the hydrophilic polymer is a copolymer including a first structural unit derived from an acrylic acid cesium salt or an acrylic acid rubidium salt and a second structural unit derived from vinyl alcohol. More preferably, the CO.sub.2 hydration catalyst has catalytic activity at a temperature of 100° C. or higher.

The invention relates to a method for the separation of isocyanate monomers from isocyanate-containing mixtures by the provision of the mixture in a solvent and dialysis of the dissolved mixture against the solvent by means of a permeable membrane having a pore size in the range of between 5 and 400 nm. The method may in particular be employed for the separation of isocyanate monomers from prepolymers containing isocyanate groups, with said prepolymers being used for the production of adhesives, insulating, and expanding foams.