A bipolar membrane BP characterized in that particles 5 of a basic metal chloride are distributed in the interface between a cation-exchange membrane 1 and an anion-exchange membrane 3.

The present invention relates to a cross-linked porous membrane from hydrolysis of ester-containing side chain and a preparation method thereof. Firstly, membrane material is obtained through copolymerization of four monomers including butyl methacrylate, styrene, sodium sulfonated styrene and vinylbenzyl chloride. In membrane formation, a small amount of lithium chloride micromolecule porogen is added and cross-linked by using tetramethyl hexamethylene diamine to prepare a nanoscale dense membrane through hydrolysis under the alkaline condition. Through the characteristic of hydrolysis of a butyl ester side chain in the polymer under the alkaline condition, the space originally occupied by the butyl ester in the hydrolyzed membrane is vacated; and after hydrolysis, with the appearance of carboxylic acid ionic conduction groups, a large quantity of ester bonds is hydrolyzed, so that the patency of ion transfer channels in the membrane is enhanced. Thus, ionic conductivity of the membrane is greatly enhanced. The nanoscale porous membrane prepared by the present invention not only has good selectivity and battery performance, but also reduces the preparation cost of the membrane to a great extent, and is suitable for application in all vanadium flow batteries.

A proton exchange composite membrane (PECM) and a method of synthesizing the membrane are disclosed. The PECM may include a PBI membrane doped with an acid, an imidazolium-based dicationic ionic liquid, and a mesoporous material. This PECM can be used as an improved high-temperature polymer electrolyte membrane (HT-PEM) fuel cell. The disclosed fuel cell can provide improved proton conductivity, acid uptake, and thermal stability.

polymeric ion-conducting membrane with an enhanced stability against attacks of free radicals for exteding its service time, which comprises (a) a polymer matrix, and (b) a redox stabilizer, where the redox stabilizer is attached to the polymer matrix by chemical or ligand bonding, or the redox stabilizer is physically mixed with the polymer matrix.

A membrane for fuel cells, such as PEM and/or AEM fuel cells and/or electrolyzers is disclosed. Such a membrane (e.g., an anion conducting membrane) may include: crosslinked ionomer comprising two types of functional groups: a first type of functional groups forming crosslinking bonds between two ionomer chains; and a second type of functional groups comprising ion conducting functional groups. In some embodiments, the crosslinking bonds may not include the ion conducting functional groups. A catalyst coated membrane (CCM) is also disclosed. In such case the membrane may further include at least one catalyst layer attached to at least one side of the membrane to form the catalyst coated membrane (CCM). The at least one catalyst layer may include catalyst nanoparticles and crosslinked ionomer of the catalyst layer comprising two types of functional groups.

A method of producing an ion-conducting membrane containing a polymer having an ionic group, involves multiple liquid treatment steps in which a precursor membrane is brought into contact with an acid treatment solution or an alkali treatment solution, the precursor membrane containing a polymer in a state in which the aforementioned ionic group forms a salt with an impurity ion, wherein the liquid treatment time in the second and subsequent liquid treatment steps of the multiple liquid treatment steps is shorter than the liquid treatment time in the initial liquid treatment step.

An anion exchange stationary phase includes a negatively charged substrate particle, a base condensation polymer layer, a crosslinked ethanolamine condensation polymer, and a glycidol condensation layer. The crosslinked ethanolamine condensation polymer layer can be covalently attached to the base condensation polymer layer. The crosslinked ethanolamine condensation polymer layer can be formed by a condensation reaction product of a polyepoxide compound and ethanolamine. The glycidol condensation layer can be formed by the treatment of glycidol. The anion exchange stationary phase are suitable for separating a variety of haloacetic acids and common inorganic anions in a single chromatographic run in less than 20 to 30 minutes.

Nanostructured polyelectrolyte bilayers deposited by Layer-by-Layer deposition on nanoporous membranes can be selectively crosslinked to modify the polyelectrolyte charge density and control ionic selectivity independent of ionic conductivity. For example, the polyelectrolyte bilayer can comprise a cationic polymer layer, such as poly(ethyleneimine), and an anionic polymer layer, such as poly(acrylic acid). Increasing the number of bilayers increases the cation selectivity when the poly(ethyleneimine) layer is crosslinked with glutaraldehyde. Crosslinking the membranes also increases the chemical and mechanical strength of the polyelectrolyte films. This controllable and inexpensive method can be used to create ion-selective and mechanically robust membranes on porous supports for a wide range of applications.

A method of producing an ion-conducting membrane containing a polymer having an ionic group, involves multiple liquid treatment steps in which a precursor membrane is brought into contact with an acid treatment solution or an alkali treatment solution, the precursor membrane containing a polymer in a state in which the aforementioned ionic group forms a salt with an impurity ion, wherein the liquid treatment time in the second and subsequent liquid treatment steps of the multiple liquid treatment steps is shorter than the liquid treatment time in the initial liquid treatment step.

The electrochemical energy conversion system of the present disclosure includes an anode, a cathode, and an ion exchange membrane including a polymer having an aromatic polymer chain and an alkylated substrate including an alkyl chain, and at least one ionic group. The alkylated substrate is bound to at least one aromatic group in the polymer chain via Friedel-Crafts alkylation of the at least one aromatic group. The alkylation reaction utilizes a haloalkylated tertiary alcohol or a haloalkylated alkene as a precursor. In the presence of an acid catalyst, a carbocation is generated in the precursor which reacts with the aromatic rings of the polymer chain. The at least one ionic group is then replaced with a desired cationic or anionic group using a substitution reaction. The membranes exhibit advantageous stability achieved through a simplified and scalable reaction scheme.