Membrane-based gas separation offers practical advantages for hydrogen (H2) and carbon dioxide (CO2) separation for steam methane reforming units. Modification of membrane materials can optimize membrane performance. In this study, the central focus is on investigating the effect of different loadings of halloysite nanotubes (HNTs) (0, 0.5, 1.0, 1.5, and 2.0 wt%) incorporated into a blend of cellulose acetate (CA) and polysulfone (PSF) polymers with the aim of improving the membrane properties. The Fourier transform infrared spectroscopy-attenuated total reflectance (FTIR-ATR) results confirmed that the primary functional groups of PSF and CA remained intact upon HNTs incorporation, with no distinct HNT peaks altering the main chemical functionalities. Field emission scanning electron microscopy- energy dispersive X-ray spectroscopy (FESEM-EDX) analyses showed that low concentrations of HNTs (0.5 wt%) improved surface smoothness and reduced macrovoids, beneficial for gas separation. Cross-sectional images of FESEM micrographs showed no evidence of obvious agglomeration, suggesting a good dispersion of HNTs. From the X-ray diffraction (XRD) analysis, all the membrane samples retained an amorphous structure, indicating that the incorporation of HNT has less effect on the polymer chain properties of the membranes.

Currently, polylactic acid (PLA) is an attractive alternative to polypropylene (PP) because of its biodegradability. This study introduces a novel modification strategy for PLA by creating a multifunctional ionization layer with ionic salts. This approach achieves humidity sensing, reliable antibacterial properties, and excellent degradability simultaneously. The modified PLA textile sensor exhibits high sensitivity to respiratory humidity (0.92 at 90% RH), with ultrafast response (0.12 s) and recovery times (0.16 s). Additionally, the textile demonstrates excellent antibacterial performance against both E. coli (99.9%) and S. aureus (99.9%) after 1 h of contact. It also shows notable biodegradability with a weight loss rate of 60.38% after 30 days. Also, the ionic salt mechanism is explained through dynamic ionization interactions attributed to the modified ionic salts, which feature both long-chain alkanes and active ions. This work presents a new method to enhance the respiratory detection and antibacterial performance of biodegradable masks.

Lithium-ion batteries (LIBs) are widely used as important energy storage and energy supply devices. The porous design and heteroatomization modification of carbon-based anode materials are crucial for achieving high-capacity and reversible energy storage in LIBs. Sol-gel method and pyrolysis treatment were used to obtain silica/silver composite particles used as templates. Polyphosphazene-coated silica/silver composite composite carbon materials (SiO2/Ag@PZS-C) were synthesized through in-situ self-assembly and carbonization of polyphosphazene. The electrochemical behavior and lithium storage mechanism of SiO2/Ag@PZS-C was also studied. The results reveal that the composite exhibited high specific capacity, stable cycling and superior rate performance. The double modification of silver nanoparticles and polyphosphazene carbon significantly improves the conductivity of silica and reduces the volume change. Moreover, the carbon shell of polyphosphazene facilitated the formation of a stable solid electrolyte interface film (SEI), preventing direct contact between the active material and the electrolyte, thereby substantially enhancing lithium storage performance.

The article gives an overview of energy storage composites, their materials, manufacturing processes, and applications. Carbon- and metal-based nanoparticles and their relevant properties are presented. We focus on multifunctional structural supercapacitors and their components. Thus, we describe the main structural electrolytes and elements of the structural electrodes. We show that the nanoparticles significantly influence the electrochemical properties of the electrode. For example, carbon-based nanoparticles can achieve low energy density but high power density, while the opposite is true for metal-based nanoparticles. We show that when carbon- and metal-based nanoparticles are used together, a positive synergy is created between them, promoting the development of favorable electrochemical properties in the electrodes. Furthermore, we present structural supercapacitors and possible ways to introduce nanoparticles into the system. Finally, we present a summary of the progress achieved so far and the advancements expected in the future, as well as potential areas where structural supercapacitors could be used.

Since the properties of polyaniline (PANI) are widely related to the type of its dopant, the present manuscript has an objective to define whether and to what extent the protic ionic liquids contribute to doping PANI. Hence, pyrrolidinium p-toluenesulfonate [Pyrr][PTS] – a protic ionic liquid – has been investigated either as a polymerisation medium or as a secondary dopant. As for the polymerisation medium, it was found that binary mixtures of [Pyrr][PTS]/water, with different weight ratios, are convenient to prepare PANI in emeraldine salt form. Furthermore, the structural analysis of the resulted PANI has revealed that the cation of [Pyrr][PTS] does not functionalise PANI backbone and [Pyrr][PTS] acts like the typical Brřnsted acid in doping PANI, regardless of the amount of [Pyrr][PTS] in the polymerisation medium. To confirm this conclusion, [Pyrr][PTS] has also been studied as a secondary dopant: the conventional PANI has been prepared, deprotonated then dispersed into [Pyrr][PTS]/water with different formulations. The results have shown that [Pyrr][PTS] leads to the formation of reprotonated PANI without altering structural change. One can thus conclude that the noncovalent functionalisation of PANI with the cation of the protic ionic liquids is not an exigent requirement to prepare the emeraldine salt form of PANI in aqueous solutions of protic ionic liquids.