This work presents a novel approach to synthesizing magnetic core-shell nanocomposites, consisting of magnetic nanoparticles and a metal-organic framework, for environmental applications. The synthesis is based on the encapsulation of magnetic Fe₃O₄ nanoparticles with microporous zeolitic imidazolate framework-8 (ZIF-8) nanocrystals via ultrasonic activation under a continuous supply of precursor solutions. This sonochemical approach is proven to be a fast, cost-effective, and controllable route for the preparation of magnet-responsive Fe₃O₄@ZIF-8 nanoparticles with a core-shell structure. The functional nanomaterial possesses a high content of ZIF-8 and combined micro/mesoporosity, and thus can be used as adsorbents that can be easily separated using a magnet. In particular, the sonochemically prepared Fe₃O₄@ZIF-8 exhibits significant adsorption performance for the removal of copper ions from water: a short adsorption time (10 min), high maximum uptake capacity (345 mg g⁻¹), and excellent removal efficiency (95.3%). These performances are interpreted and discussed based on the materials characteristics of Fe₃O₄@ZIF-8 established by microscopy, gas sorption, X-ray diffraction, and thermal analysis.

Ion conducting membranes play a crucial role in redox flow batteries, separating anolyte and catholyte while allowing proton transport to complete the circuit. However, most membranes are trapped in a trade‐off relation and show either low conductivity or high vanadium crossover. This study investigates the use of dense sulfonated para‐polybenzimidazole membranes for vanadium redox flow batteries (VRFBs), and analyzes the effects of membrane preparation process, membrane thickness and operating temperature on the VRFB performance. The results demonstrate superior performance of VRFBs utilizing fluorine‐free sulfonated para‐polybenzimidazole membranes compared to other types. Under optimal conditions, the VRFB exhibits high coulombic efficiency (>99%) and high energy efficiency (EE, 92.2% at a current density of 80 mA cm⁻²), and durability. The achieved EE represents one of the highest reported in the literature for VRFBs. In addition, it is shown that operation at 35 °C has benefits at high current densities (EE at 300 mA cm⁻² is over 80% at 35 °C but 72% at 25 °C), while the operation at 80 mA cm⁻² only shows a small temperature effect (91.8 and 92.2%, respectively).

Naturally abundant vermiculite clay was expanded by using an aqueous solution of H₂O₂ and its surface was modified with ultra-thin polydimethylsiloxane (PDMS) using facile thermal vapor deposition to prepare an ecologically friendly, low-cost oil sorbent that plays an important role in oil spillage remediation. The resulting PDMS-coated expanded vermiculite (eVMT@PDMS) particles exhibited adequate hydrophobicity and oleophilicity for oil/water separation, with numerous conical slit pores (a size of 0.1–100 μm) providing a great sorption capacity and an efficient capillarity-driven flow pathway for oil collection. Simply with using a physically-packed eVMT@PDMS tube (or pouch), selective oil removals were demonstrated above and beneath the surface of the water. Furthermore, these sorbents were successfully integrated and then applied to the advanced oil-collecting devices such as a barrel-shaped oil skimmer and a self-primed oil pump.

Poly(4,4′‐diphenylether‐5,5′‐bibenzimidazole), OPBI, is sulfonated at different conditions to reach different degrees of sulfonation (DOS of 35, 54, 102, and 133%). The membrane with a DOS of 102% shows the most balanced properties. The tensile strength is 55 MPa and the elongation at break is 130%. Conductivity in 3 m sulfuric acid exceeds that of Nafion 212 (58 mS cm⁻¹) and reaches 70 mS cm⁻¹. The resistance of a 23 µm thick membrane is 33 mΩ cm², and energy efficiencies of 91.8% at 80 mA cm⁻² and 90.4% at 100 mA cm⁻² are achieved. OPBI showed the highest stability in contact with VO₂⁺, because the ions cannot enter the membrane. Sulfonated OPBI swells more in sulfuric acid, and therefore has a lower stability. However, it is found that the stability increases with the DOS. This indicates that attack by VO₂⁺ occurs preferentially at positions that are activated for electrophilic aromatic substitution reactions.