In this work, thermoplastic polyurethane (TPU) composites incorporated with 1.0 wt% Cu particles were synthesized by the melt blending method. The effect of the incorporated copper particle size on the antibacterial, thermal, rheological, and mechanical properties of TPU was investigated. The obtained results showed that (i) the addition of copper particles increased the thermal and mechanical properties because they acted as co-stabilizers of polyurethane (PU) (ii) copper nanoparticles decreased the viscosity of composite melts, and (iii) microparticles > 0.5 µm had a tendency to easily increase the maximum torque and formation of agglomerates. SEM micrographics showed that a good mixture between TPU and copper particles was obtained by the extrusion process. Additionally, copper-TPU composite materials effectively inhibited the growth of the Gram-negative Escherichia coli and the Gram-positive Staphylococcus aureus. Considering that the natural concentration of copper in the blood is in the range of 0.7–0.12 mg/L and that the total migration value of copper particles from TPU was 1000 times lower, the results suggested that TPU nanocomposites could be adequately employed for biomedical applications without a risk of contamination.

The microbial fuel cells (MFCs) which demonstrates simultaneous production of electricity and wastewater treatment have been considered as one of the potential and greener energy production technology among the available bioelectrochemical systems. The air-cathode MFCs have gained additional benefits due to using air and avoiding any chemical substances as catholyte in the cathode chamber. The sluggish oxygen reduction reaction (ORR) kinetics at the cathode is one of the main obstacles to achieve high microbial fuel cell (MFC) performances. Platinum (Pt) is one of the most widely used efficient ORR electrocatalysts due to its high efficient and more stable in acidic media. Because of the high cost and easily poisoned nature of Pt, several attempts, such as a combination of Pt with other materials, and using non-precious metals and non-metals based electrocatalysts has been demonstrated. However, the efficient practical application of the MFC technology is not yet achieved mainly due to the slow ORR. Therefore, the review which draws attention to develop and choosing the suitable cathode materials should be urgent for the practical applications of the MFCs. In this review article, we present an overview of the present MFC technology, then some significant advancements of ORR electrocatalysts such as precious metals-based catalysts (very briefly), non-precious metals-based, non-metals and carbon-based, and biocatalysts with some significant remarks on the corresponding results for the MFC applications. Lastly, we also discussed the challenges and prospects of ORR electrocatalysts for the practical application of MFCs.

This review provides an overview of recent advancements in cathode materials for proton exchange membrane fuel cells (PEMFCs), focusing on their role in catalyzing the oxygen reduction reaction (ORR). This begins with a fundamental discussion of the ORR mechanism, including two‐electron and four‐electron pathways. The review then explores a wide range of electrocatalyst materials, starting with precious metal catalysts, particularly platinum‐based materials, along with alloying strategies and composite structures. This then delves into nonprecious metal catalysts, encompassing metal‐free ORR electrocatalysts, carbon‐supported composite materials (including heteroatom doping and metal‐carbon composites), and transition metal oxides. The review further examines metal phthalocyanines, biomass‐derived catalysts, bimetallic and trimetallic nanoparticles supported on carbon matrices, and chalcogenides (oxides, sulfides, and selenides) as ORR electrocatalysts. Advanced materials such as single‐ and dual‐atom catalysts, high‐entropy alloys, and metal organic frameworks derived electrocatalysts are also discussed. We analyze the identification of reaction sites and the effect of structure on catalytic activity. Furthermore, the review covers electrochemical measurements in PEMFCs and explores technological applications and industrial relevance, including products and patents. Finally, this review concludes by addressing future perspectives and challenges in the field of cathode materials for PEMFCs.

By this work, we intended to understand the effect of ultrasonic sonication time on the structural and morphological properties of cerium oxide (ceria) nanoparticles. For comparison ceria nanoparticles synthesized by coprecipitation technique were considered. A series of controlled experiments were carried out to understand the crucial factors that inluenced the formation of ceria nanostructures under a determined sonication time. The average crystallite size and the microstrain were obtained from W-H analysis of the X-ray diffraction (XRD) data. The variation in the bandgap values was discussed with respect to the crystallite size. For antibacterial studies, two known bacteria Escherichia coli (ATCC 25922) and Staphylococcus aureus (ATCC 25923) were used. On E. coli, the prepared ceria showed bactericidal properties at 1000 (μg mL^-1), ceria obtained by sonication for 30 min was bactericidal at 2000 (μg mL^-1) and ceria made by sonication for 60 and 120 min were bactericidal at 3000 (μg mL^-1). While on S. aureus all the experimental conditions showed bacterial death at 3000 (μg mL^-1). The influence of the sonication time on the structural and antibacterial properties were discussed.