A functional polymer membrane having a pore volume fraction of 0.6% or more and 3.0% or less by allowing a reaction of curing a composition containing a polymerizable compound (A) and a copolymerizable monomer (B).

Embodiments provide a filter with a generally rectangular, non-cylindrical profile. The filter may have multiple pleat packs positioned between pleat covers that define regions and flow channels in a cavity of the filter body. The pleat covers have openings that allow a fluid to flow through the multiple pleat packs via parallel flows or series flows. End caps bonded to the body define flow passages for directing the fluid from an inlet to an outlet via the pleat packs for series or parallel filtration. The pleat packs may be made of the same or different materials and may be configured with the same or different heights based on flow requirements. A cage or a separator may be positioned between the pleat packs. The pleat packs may be made of a continuous pleated membrane with bridges defining a space between the pleat packs to accommodate the cage or separator.

Disclosed is a porous support including fine porous structures formed between nanofibers, wherein the fine porous structures have a porosity of 50% to 90%, a pore size of 0.01 μm to 10 μm and an air permeability of 0.01 to 7 sec/100 cc.Math.air, and the porous support has a thickness of 5 μm to 50 μm, a method of manufacturing the same and a reinforced membrane including the same.

The invention discloses a separation matrix comprising a plurality of multimodal ligands covalently coupled to a support, wherein said support is a membrane comprising nonwoven polymer fibers and wherein said ligands are capable of interacting with a target biomacromolecule. Further, the invention discloses separation methods using the separation matrix.

In this disclosure, a process of recycling acid, base and the salt reagents required in the Li recovery process is introduced. A membrane electrolysis cell which incorporates an oxygen depolarized cathode is implemented to generate the required chemicals onsite. The system can utilize a portion of the salar brine or other lithium-containing brine or solid waste to generate hydrochloric or sulfuric acid, sodium hydroxide and carbonate salts. Simultaneous generation of acid and base allows for taking advantage of both chemicals during the conventional Li recovery from brines and mineral rocks. The desalinated water can also be used for the washing steps on the recovery process or returned into the evaporation ponds. The method also can be used for the direct conversion of lithium salts to the high value LiOH product. The method does not produce any solid effluent which makes it easy-to-adopt for use in existing industrial Li recovery plants.

Provided is a cation exchange membrane having a stable ion exchange performance during usage, being excellent in basic properties such as membrane resistance and ion transportation as well as strength, and useful for electrodialysis and a method for producing the same. The cation exchange membrane is composed of a polyvinyl alcohol copolymer including an anionic group-containing anionic polymer segment and a vinyl alcohol polymer segment, and having a microphase separation structure having a domain size (X) in a range from 0 nm<X≦150 nm. The method is composed of forming a membrane from a polyvinyl alcohol copolymer which is adjusted to contain salts in a proportion that the salt weight (C) relative to the polyvinyl alcohol copolymer weight (P) is [(C)/(P)] of 4.5/95.5 or lower.

A crosslinked copolymer is provided, which includes a copolymer crosslinked by a crosslinking agent. The copolymer is copolymerized of (a) styrene-based monomer, (b) monomer having conjugated double bonds or acrylate ester monomer, and (c) ammonium-containing heterocyclic monomer. The crosslinking agent is (d) ##STR00001##
or the product of the reaction between ##STR00002##
and (e) ##STR00003##
or a combination thereof. Z is ##STR00004##
wherein each R.sup.1 is independently H or C.sub.1-4 alkyl group, each R.sup.2 is independently H or C.sub.1-4 alkyl group, R.sup.3 is single bond, —O—, —S—, —CH.sub.2—, or —NH—. n is a positive integer. x is 1 to 12, y is 1 to 5, and z is 1 to 5.

A conductive nanoporous membrane system has a first ion exchange membrane formed from a nanoporous substrate that is coated with a metal or carbon or conductive polymers to form a conductive membrane, a second ion exchange membrane that is also formed from a nanoporous substrate coated with a metal to form a conductive membrane is positioned in spaced relation to the first conductive membrane and coupled to a voltage source; the negatively potential membrane acts as a cation exchange membrane in the presence of an electrolyte, and the positively connected electrode behave as anodic exchange membrane in the presence of an electrolyte due to the formation of electrical double layers at the interface between metal and liquid electrolyte.

A photodialysis device that can desalinate saline streams is described herein. The device can have a desalination rate that is significantly faster than current solar thermal desalination technology. Salt is removed from water by passing ionic current derived from sunlight through this water using dye-sensitized membranes. The device can serve as a distributed, low-cost technology that can efficiently and effectively desalinate low salinity sources of water, which is particularly useful for agriculture and drinking water applications.

The present disclosure relates to membranes for use in electrolysis systems. The teachings thereof may be embodied in a method for checking a membrane of an electrolyzer comprises two volumes separated by the membrane and produces two product gases from a starting liquid. The method may include: detecting an electrolysis current strength during electrolysis, measuring a liquid flow rate of the starting liquid between the two electrolyzer volumes, calculating a ratio of the measured liquid flow rate and the detected electrolysis current strength, and using the calculated ratio as an indication of membrane leaktightness.