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Non-aqueous redox flow batteries (NARFBs) have been attracting much attention because they can significantly increase power and energy density compared to conventional RFBs. In this study, novel pore-filled anion-exchange membranes (PFAEMs) for application to a NAPFB employing metal polypyridyl complexes (i.e., Fe(bpy)32+/Fe(bpy)33+ and Co(bpy)32+/Co(bpy)33+) as the redox species are successfully developed. A porous polyethylene support with excellent solvent resistance and mechanical strength is used for membrane fabrication. The PFAEMs are prepared by filling an ionic liquid monomer containing an imidazolium group and a crosslinking agent into the pores of the support film and then performing in situ photopolymerization. As a result, the prepared membranes exhibit excellent mechanical strength and stability in a non-aqueous medium as well as high ion conductivity. In addition, a low crossover rate for redox ion species is observed for the prepared membranes because they have relatively low swelling characteristics in non-aqueous electrolyte solutions and low affinity for the metal-complex redox species compared to a commercial membrane. Consequently, the PFAEM is revealed to possess superior battery performance than a commercial membrane in the NARFB tests, showing high energy efficiency of about 85% and stable operation for 100 cycles. [ABSTRACT FROM AUTHOR]

Non-aqueous redox flow batteries (NARFBs) have been attracting much attention because they can significantly increase power and energy density compared to conventional RFBs. In this study, novel pore-filled anion-exchange membranes (PFAEMs) for application to a NAPFB employing metal polypyridyl complexes (i.e., Fe(bpy)32+/Fe(bpy)33+ and Co(bpy)32+/Co(bpy)33+) as the redox species are successfully developed. A porous polyethylene support with excellent solvent resistance and mechanical strength is used for membrane fabrication. The PFAEMs are prepared by filling an ionic liquid monomer containing an imidazolium group and a crosslinking agent into the pores of the support film and then performing in situ photopolymerization. As a result, the prepared membranes exhibit excellent mechanical strength and stability in a non-aqueous medium as well as high ion conductivity. In addition, a low crossover rate for redox ion species is observed for the prepared membranes because they have relatively low swelling characteristics in non-aqueous electrolyte solutions and low affinity for the metal-complex redox species compared to a commercial membrane. Consequently, the PFAEM is revealed to possess superior battery performance than a commercial membrane in the NARFB tests, showing high energy efficiency of about 85% and stable operation for 100 cycles.

The development of affordable, intelligent dual-separation technology is crucial for the treatment of oil-water mixtures. Pyridinium-based poly(ionic liquid)s (PILs), designed using molecular theory, exhibit unique switching wettability properties, making them ideal for use in both aqueous and oily environments. By prewetting the material's surface with water or oil, the targeted separation of these components becomes feasible. PILs are synthesized through the cross-linking of [Pyr]Cl with various cross-linkers and auxiliary agents. Studies on the wetting mechanism of these materials have identified bursting pressure and surface structure as key factors influencing their wetting properties. They exhibit hydrophilic and lipophilic properties in air, hydrophobic properties under oil, and oleophobic properties under water, achieving a 99% separation efficiency. A reusability study demonstrated maintenance of 90% efficiency after 10 cycles, highlighting their sustained high performance. This research presents promising avenues for the application of PIL-based materials in oil-water separation, environmental remediation, and industrial processing.

We aimed to improve the imprinting effect of ionic liquid molecularly imprinted polymers (MIPs) by use of a molecular crowding agent. The ionic liquid 1-vinyl-3-ethylimidazolium tetrafluoroborate ([VEIm][BF]) was used as the functional monomer and aesculetin was used as the template molecule in a crowding environment, which was made up of a tetrahydrofuran solution of polystyrene. The ionic liquid MIPs that were prepared in the crowding environment displayed an enhanced imprinting effect. NMR peak shifts of active hydrogen of aesculetin suggested that interaction between the functional monomer and the template could be increased by the use of a crowding agent in the self-assembly process. The retention and selectivity of aesculetin were affected greatly by high molecular crowding, the amount of high molecular weight crowding agent, and the ratio of [VEIm][BF] to aesculetin. The optimal MIPs were used as solid-phase extraction sorbents to extract aesculetin from Cichorium glandulosum. A calibration curve was obtained with aesculetin concentrations from 0.0005 to 0.05 mg mL (correlation coefficient R of 0.9999, y = 1519 x + 0.0923). The limit of quantification was 0.12 μg mL, and the limit of detection was 0.05 μg mL. The absolute recovery of aesculetin was (80 ± 2)% ( n = 3), and the purity of aesculetin was (92 ± 0.5)% ( n = 5). As a conclusion, molecular crowding is an effective approach to obtain ionic liquid MIPs with high selectivity even in a polar solvent environment. [ABSTRACT FROM AUTHOR]

Ionic liquid monomers substituted with a polymerizable group were polymerized using free radical polymerization and group transfer polymerization mechanisms. Homopolymers containing a polycation or a polyanion structure were made as well as various copolymers. The latter include statistical copolymers, alternating copolymers, and block copolymers. The new polymers obtained may become of interest for application as binders for coatings. Furthermore, glass transition temperature of the polymers obtained was discussed as an important parameter for the application temperature needed for film formation. It was shown that a variation of the ionic liquid monomer structure affects the glass transition temperature of the polymer obtained. Moreover, antimicrobial properties of selected polymers were investigated using Escherichia coli and Micrococcus luteus . The results show significant differences in the antimicrobial properties of the polymers investigated. This is highly interesting for applications in which these polymers function as binders in coatings. [ABSTRACT FROM AUTHOR]