The present disclosure provides an ion-exchange membrane that includes a supporting substrate impregnated with an ion-exchange material. The supporting substrate includes an imprinted non-woven layer, and the imprinting includes a plurality of deformations at a surface density of at least 16 per cm.sup.2. The supporting substrate may lack a reinforcing layer. In some examples, the supporting substrate may include only a single layer of the imprinted non-woven fabric.

A hydrophobic biofilm membrane modified with a spiropolyurethane may be used for desalination of salt water to fresh water. The spiropolyurethane component of the membrane can produce a hydrophobic spin membrane boundary which attracts saline water, and where the hydrophobic spin membrane boundary can comprise a hinge-like motion for capture of salt molecules via a loose pore-gate spongy membrane surface texture while allowing desalinated water to flow through the porous membrane. The membrane is useful in both reverse osmosis (RO) and membrane distillation (MD) separations, including the desalination.

Nanoporous selective sol-gel ceramic membranes, selective-membrane structures, and related methods are described. Representative ceramic selective membranes include ion-conductive membranes (e.g., proton-conducting membranes) and gas selective membranes. Representative uses for the membranes include incorporation into fuel cells and redox flow batteries (RFB) as ion-conducting membranes.

A filter device includes one or more filter membranes, and a filter housing enclosing the one or more filter membranes. Each of the filter membranes includes a base membrane made of a ceramic material, and a plurality of through holes. The base membrane is coated with a coating material.

This invention relates to a novel conductive organic membrane-coupled filtration system for the degradation of organic pollutants from wastewater. The system comprises a connected water pump and a reactor. The upper end of the reactor contained a water inlet, and the lower end consisted of a water outlet. A counter electrode and a membrane electrode are fixed on the reactor between the water inlet and water outlet. The counter electrode and membrane electrode constitute a two-electrode system connected to an external potentiostat through metal wires. The membrane electrode is made of carbon-based polyvinylidene fluoride (PVDF) membrane that can be used to enhance the electrochemical separation of small molecules and the removal of organic pollutants.

Disclosed is the preparation of composite membranes formed by a tailored selective chemical modification of an ultra-thin nanoporous surface layer of a semi-crystalline mesoporous poly (aryl ether ketone) membrane with graded density pore structure. The composite separation layer is synthesized in situ on the poly (aryl ether ketone) substrate surface and is covalently linked to the surface of the semi-crystalline mesoporous poly (aryl ether ketone) membrane. Hollow fiber configuration is the preferred embodiment of forming the functionalized the poly (aryl ether ketone) membranes. Composite poly (aryl ether ketone) membranes of the present invention are particularly useful for a broad range of fluid separation applications, including organic solvent ultrafiltration and nanofiltration to separate and recover active pharmaceutical ingredients.

A composite membrane comprising: a) a first layer comprising a first porous support and a first ionic polymer present in the pores of the first porous support; b) a second layer comprising a second porous support and a second ionic polymer present in the pores of the second porous support; c) a third layer comprising a third porous support, a third ionic polymer and a fourth ionic polymer, wherein the third ionic polymer is present in the pores of the third porous support; wherein: (i) one of the first ionic polymer and the second ionic polymer is a cationic polymer and the other is an anionic polymer; (ii) the third layer c) is interposed between the first layer a) and the second layer b); (iii) the third ionic polymer comprises a network of pores and the fourth ionic polymer is present within the pores of the third ionic polymer; and (iv) one of the third ionic polymer and the fourth ionic polymer is a cationic polymer and the other is an anionic polymer.

A membrane comprising: a) a first layer comprising a first polymer or a fourth polymer having ionic groups of polarity opposite to the polarity of the ionic groups of the third polymer; b) a second layer comprising a second polymer having ionic groups of polarity the same as the polarity of the ionic groups of the third polymer; and c) a third layer comprising a co-continuous polymeric network of (i) a third polymer having ionic groups and a network of pores; and (ii) a fourth polymer having ionic groups of polarity opposite to the polarity of the ionic groups of the third polymer; wherein layer c) is interposed between layer a) and layer b) and the third polymer is obtainable by a process comprising phase separation of the third polymer from a curable composition used to prepare the third polymer.

The disclosure of the present invention relates to a method for preparing membrane and associated membrane and filter element. The method comprises providing a porous substrate having a plurality of pores; and applying a pre-filler solution to at least partially occupy the pores in the porous substrate. The membrane comprises a porous substrate and a filter layer formed on the porous substrate. The filter element comprises a core tube; and a membrane as prepared and rolled around the core tube.

Provided are a monovalent anion selective ion exchange membrane and a method of manufacturing the ion exchange membrane. In regard to the monovalent anion selective ion exchange membrane, a surface portion thereof has a high amount ratio of a cation exchange polymer electrolyte, a central portion thereof has a high amount ratio of an anion exchange polymer electrolyte, and an amount ratio of the anion exchange polymer electrolyte with respect to the cation exchange polymer electrolyte continuously increases in the thickness direction thereof from the surface toward the center. Due to this structure, compared to monovalent anions, polyvalent anions may permeate much less through the exchange membrane. Thus, high selectivity for monovalent anions may be obtained.