An active CO.sub.2 capture unit for capturing CO.sub.2 from a dilute source of CO.sub.2 input gas can include an inlet through which an input gas is introduced into the unit and a non-aqueous region comprising a non-aqueous CO.sub.2 binding organic liquid containing OH.sup.− arranged to be in contact with the input gas to chemisorb CO.sub.2 from the input gas and convert the chemisorbed CO.sub.2 into HCO.sub.3.sup.− by reacting with OH.sup.−. The unit also includes an aqueous region arranged downstream of the non-aqueous region, wherein at an aqueous region interface, the HCO.sub.3.sup.− interacts with H.sub.2O and decomposes to CO.sub.2 and CO.sub.3.sup.2−. An anion exchange membrane is disposed between the non-aqueous region and the aqueous region to facilitate HCO.sub.3.sup.− diffusion and migration from the non-aqueous region to the aqueous region. A captured CO.sub.2 outlet is disposed downstream of the aqueous region.

A composition is disclosed comprising a sulfonated styrenic block copolymer (SSBC) having an ion exchange capacity (IEC) of at least 0.5 meq/g; and at least one compound which reacts with the SSBC forming a cross-linked SSBC. The compound is selected from: (i) a cross-linking agent, (ii) a metal cation, and (iii) a non-sulfonated polymer. A film prepared from the composition containing the cross-linked SSBC has a toughness in wet state measured after 1 week of 1.2 to 8 MJ/m.sup.3; and a tensile stress in wet state measured after 1 week of 3.2 to 8 MPa, according to ASTM D412. The film can be used as a water 10 purification membrane or an antimicrobial protection layer.

An electrochemical system utilizes an anion conducting layer disposed between an anode and a cathode for transporting a working fluid. The working fluid may include carbon dioxide that is dissolved in water and is partially converted to carbonic acid that is equilibrium with bicarbonate anion. An electrical potential across the anode and cathode creates a pH gradient that drives the bicarbonate anion across the anion conducting layer to the cathode, wherein it is reformed into carbon dioxide. Therefore, carbon dioxide is pumped across the anion conducting layer.

The disclosure relates to a hydrogenated styrene-based multiblock copolymer composition, having selectively quaternized midblock, for forming anion-exchange membranes (AEMs). The quaternized hydrogenated styrene-based multiblock copolymer is characterized as having a high glass transition temperature from the hydrophobic end-blocks, low vinyl (rubber) content, and quaternized mid-block. AEMs made from the composition have improved thermal and dimensional stability in electrolyzer operations.

An electrochemical cell comprising a membrane electrode assembly and a selectively permeable barrier layer comprising sulfonated polymer is disclosed. The selectively permeable barrier layer is arranged facing at least one electrocatalyst layer, e.g., anode or cathode. The sulfonated polymer layer aids in controlling the movement of fluids and/or their constituents into and out of the electrochemical cell assembly for separation or capture for subsequent use.

A single piece-type bipolar film roll with a mesh cloth support and a manufacturing method therefor. The single piece-type bipolar film roll is supported by a high-strength ultra-high molecular weight polyethylene mesh cloth, one side of the single piece-type bipolar film roll is a cation exchange layer containing a benzenesulfonic acid group, the other side of the single piece-type bipolar roll is an anion exchange layer containing a benzyl dimethyl butyl ammonium quaternary amino group, and the middle is a water dissociation catalyst layer containing a benzyl methyl butyl amine tertiary amino group, and the three layers form the single piece-type bipolar film roll. By providing a wider protective film and a narrower spacing film, a dipping and absorbing film roll is polymerized to prepare a composite base film roll which is then subjected to continuous sulfonation to prepare a single-sided sulfonated composite positive film roll, and then the unreacted blank side is sequentially subjected to three-step chemical reactions such as complete chloromethylation, complete tertiary amination and incomplete methylation, so as to prepare a single piece-type bipolar film roll having a compact structure, a clear middle interface, a high mechanical strength and a stable quaternary amino group, and the product qualification rate is high; and the single piece-type bipolar film roll is suitable for a bipolar film electrodialysis engineering application of an organic material-containing system.

A preparation method of a gradient long-effective catalytic membrane with high-strength and anti-deposition property is provided and includes: adding a nanometal oxide catalyst into an N, N-dimethylformamide solution of polyacrylonitrile or polystyrene, uniformly mixing, performing electrostatic spinning, keeping a receiver at −190° C. to −200° C. in the electrostatic spinning process, and performing freeze drying on a precursor membrane obtained after the electrostatic spinning is finished, so as to obtain the gradient long-effective catalytic membrane. According to the method, the gradient long-effective catalytic membrane with high-strength and anti-deposition property is obtained through a one-step method which adopts an ultralow-temperature-electrostatic spinning technology and combines with nanometal, the contradictory relation between the catalytic efficiency and the membrane stability in a traditional catalytic membrane is solved, the catalytic performance of the membrane is fully played, the organic polluted wastewater can be efficiently catalytically degraded, and the service life of the catalytic membrane is prolonged.

The present disclosure provides an efficient and stable magnetic nanofiber membrane and a preparation method and use thereof, and belongs to the technical field of composites. The preparation method includes the following steps: dissolving polyacrylonitrile or polystyrene, nZVI particles, and n-octyltrimethylammonium bromide in N,N-dimethylformamide, and mixing uniformly to obtain a spinning solution; subjecting the spinning solution to electrospinning; and vacuum-drying a resulting fiber membrane to obtain the efficient and stable magnetic nanofiber membrane. In the present disclosure, the magnetic nanofiber membrane has a high specific surface area, a desirable porosity, an excellent mechanical strength, and satisfactory magnetic properties. The membrane effectively exerts a synergistic effect of the nZVI particles and an organic polymer material carrier, avoids easy oxidation of a catalyst surface and easy particle agglomeration, enhances a catalytic activity of the magnetic nanofiber membrane, and improves an efficiency in organic wastewater treatment.

A preparation method of a gradient long-effective catalytic membrane with high-strength and anti-deposition property is provided and includes: adding a nanometal oxide catalyst into an N, N-dimethylformamide solution of polyacrylonitrile or polystyrene, uniformly mixing, performing electrostatic spinning, keeping a receiver at −190° C. to −200° C. in the electrostatic spinning process, and performing freeze drying on a precursor membrane obtained after the electrostatic spinning is finished, so as to obtain the gradient long-effective catalytic membrane. According to the method, the gradient long-effective catalytic membrane with high-strength and anti-deposition property is obtained through a one-step method which adopts an ultralow-temperature-electrostatic spinning technology and combines with nanometal, the contradictory relation between the catalytic efficiency and the membrane stability in a traditional catalytic membrane is solved, the catalytic performance of the membrane is fully played, the organic polluted wastewater can be efficiently catalytically degraded, and the service life of the catalytic membrane is prolonged.

The invention relates to:—anion exchange blend membranes consisting the following blend components:—a halomethylated polymer (a polymer with —(CH2)x—CH2—Hal groups, Hal=F, CI, Br, I; x=0-12), which is quaternised with a tertiary or a n-alkylated/n-arylated imidazole, an N-alkylated/N-arylated benzimidazole or an N-alkylated/N-arylated pyrazol to form an anion exchanger polymer. - an inert matrix polymer in which the anion exchange polymer is embedded and which is optionally covalently crosslinked with the halomethylated precursor of the anion exchanger polymer,—a polyethyleneglycol with epoxide or halomethyl terminal groups which are anchored by reacting with N—H-groups of the base matrix polymer using convalent cross-linking—optionally an acidic polymer which forms with the anion-exchanger polymer an ionic cross-linking (negative bound ions of the acidic polymer forming ionic cross-linking positions relative to the positive cations of the anion-exchanger polymer)—optionally a sulphonated polymer (polymer with sulphate groups —SO2Me, Me=any cation), which forms with the halomethyl groups of the halomethylated polymer convalent crosslinking bridges with sulfinate S-alkylation. The invention also relates to a method for producing said membranes, to the use of said membranes in electrochemical energy conversion processes (e.g. Redox-flow batteries and other flow batteries, PEM-electrolyses, membrane fuel cells), and in other membrane methods (e.g. electrodialysis, diffusion dialysis).