The present application discloses a composite reverse osmosis membrane and a preparation method thereof. The method includes: uniformly mixing fluorine-containing polyaryletherketone of a certain concentration and silane-modified polyaryletherketone as a casting solution; coating a non-woven fabric, i.e., a substrate, with the casting solution to form a support layer; then coating the surface of the support layer with a solution A and a solution B sequentially for reaction to form a polyamide desalination layer; and coating the polyamide desalination layer with a modified polyvinyl alcohol anti-pollution layer. By means of the method, the composite reverse osmosis membrane is prepared. Compared with the prior art, the present application can prepare a composite reverse osmosis membrane with high temperature resistance and high strength by using the composite modified polyaryletherketone as the support layer, and moreover, uses polyvinyl alcohol as a component of the anti-pollution layer, and has good anti-pollution properties.

A thin-film composite polyamide reverse osmosis membrane with anti-bacterial and anti-biofouling effects and a preparation method thereof are disclosed. The preparation method includes: dissolving a highly water-stable metal organic framework CuBTTri in an n-hexane solution containing trimesoyl chloride by ultrasonic wave, immersing a polyethersulfone ultrafiltration membrane in an aqueous solution of m-phenylene diamine and taking out, and then immersing the ultrafiltration membrane in the trimesoyl chloride-n-hexane solution containing the aforementioned metal organic framework for reaction and modification, so as to obtain the thin-film composite polyamide reverse osmosis membrane. The resulting composite reverse osmosis membrane integrated with the anti-bacterial metal organic framework CuBTTri has a high reverse osmosis membrane permeability and possesses greatly improved and persistent anti-bacterial and anti-biofouling properties. The preparation method is simple and conducive to promotion, and has mild conditions.

Apparatuses and methods for fabricating thin film composite hollow fiber membranes. In some implementations, an apparatus is used to remove excess first solution from a hollow fiber that has been immersed in a first solution. In some implementations, the method and apparatuses include flowing a gas, for example, compressed gas or ambient air, past a surface of a hollow fiber that has been immersed in a first solution prior to immersion in a second solution. In some implementations, the gas is flowed past the surface under positive pressure, while in other implementations the gas is flowed under negative pressure, for example, vacuum. The apparatuses and devices can be used to produce thin film composite hollow fiber membranes without pressing or damaging the hollow fiber.

A method for in situ production of antimicrobial filtration membranes that uses self-assembly of surfactants such as block copolymers as a template. The mesophase structure (for example hexagonal or lamellar) can be determined, and membrane pore size can be controlled in the nanometer range, by changing the block copolymer and the amounts of the components such as the block copolymer, aqueous solution, monomer, crosslinker, and initiator. The monomer phase cures in the template and there is no need for organic solvents and coagulation bath or other post-modification. As-synthesized membranes were found to have pore sizes with a narrow size distribution in the range of 3-4 nm with a molecular weight cutoff of 1500 g/mol and displayed both excellent fouling resistance and high permeance of water, vastly outperforming a conventional NIPS UF membrane. The monomer can comprise a quaternary ammonium group so that the membrane is antibacterial. The block copolymer can comprise hydrophilic blocks which form the surfaces of the membrane pores, rendering them hydrophilic.

The present invention relates to a composite semipermeable membrane including: a substrate; a porous support layer disposed on the substrate; and a separation functional layer disposed on the porous support layer, in which the separation functional layer includes: a first layer including a crosslinked aromatic polyamide; and a coating layer existing on the first layer and including an aliphatic polyamide including a fluorine atom, and the composite semipermeable membrane has a proportion of the number of fluorine atoms to the total number of atoms of all elements of 0.5% or more and 8% or less, and has a ratio (N/O ratio) of the number of nitrogen atoms to the number of oxygen atoms of 0.8 or more and 1.3 or less.

A monovalent selective ion exchange membrane is disclosed. The membrane includes a polymeric microporous substrate, a cross-linked ion-transferring polymeric layer on a surface of the substrate, and a charged functionalizing layer covalently bound to the ion-transferring layer. A method of producing a monovalent selective cation exchange membrane is also disclosed. The method may include chemically adsorbing a styrene intermediate layer to a cross-linked ion-transferring polymeric layer on a surface of a polymeric microporous substrate, chlorosulfonating the styrene intermediate layer to attach a sulfonyl chloride group layer, aminating the sulfonyl group layer to attach an amine group layer, and functionalizing the amine group layer with a charged compound layer to produce the cation exchange membrane. Water treatment systems including the monovalent selective cation exchange membrane and methods of facilitating water treatment including providing the monovalent selective cation exchange membrane are also disclosed.

A monovalent selective ion exchange membrane is disclosed. The membrane includes a polymeric microporous substrate, a cross-linked ion-transferring polymeric layer on a surface of the substrate, and a charged functionalizing layer covalently bound to the ion-transferring layer by an acrylic group. A method of producing a monovalent selective cation exchange membrane is also disclosed. The method may include chemically adsorbing an acrylic intermediate layer comprising a chlorosulfonated methacrylate group to a cross-linked ion-transferring polymeric layer on a surface of a polymeric microporous substrate, aminating the chlorosulfonated methacrylate group to attach an amine group layer, and functionalizing the amine group layer with a charged compound layer to produce the cation exchange membrane. Water treatment systems including the monovalent selective cation exchange membrane and methods of facilitating water treatment including providing the monovalent selective cation exchange membrane are also disclosed.

A novel process for making PBI films starting from gel PBI membranes polymerized and casted in the PPA process wherein acid-imbibed gel PBIs are neutralized in a series of water baths and undergo controlled drying in association with a substrate material, yielding a PBI film without the use of organic solvents.

A composite reverse osmosis membrane having a semipermeable bilayer polyamide composition comprising a base layer containing a rigid crosslinked aromatic polyamide and a top layer containing a flexible aliphatic polyamide is disclosed, the two layers in combination providing reduced salt passage in reverse osmosis desalination of brackish waters and of seawater.

Spiral wound reverse osmosis devices with reduced lateral leakage and thereby increased salt rejection are made by compacting a microporous layer within a composite reverse osmosis membrane longitudinally along its lengthwise periphery. Means and method for causing longitudinal indentations in composite membranes during manufacturing operations are disclosed and described.