Cellulose-derived battery separators have emerged as a viable sustainable alternative to conventional synthetic materials like polypropylene and polyethylene. Sourced from renewable and biodegradable materials, cellulose derivatives—such as nanofibers, nanocrystals, cellulose acetate, bacterial cellulose, and regenerated cellulose—exhibit a reduced environmental footprint while enhancing battery safety and performance. One of the key advantages of cellulose is its ability to act as a hybrid separator, using its unique properties to improve the performance and durability of battery systems. These separators can consist of cellulose particles combined with supporting polymers, or even a pure cellulose membrane enhanced by the incorporation of additives. Nevertheless, the manufacturing of cellulose separators encounters obstacles due to the constraints of existing production techniques, including electrospinning, vacuum filtration, and phase inversion. Although these methods are effective, they pose challenges for large-scale industrial application. This review examines the characteristics of cellulose and its derivatives, alongside various processing techniques for fabricating separators and assessing their efficacy in battery applications. Additionally, it will consider the environmental implications and the primary challenges and opportunities associated with the use of cellulose separators in energy storage systems. Ultimately, the review underscores the significance of cellulose-based battery separators as a promising approach that aligns with the increasing demand for sustainable technologies in the energy storage domain.

Discharging oil-contaminated wastewater into the environment without adequate treatment can have a negative impact on water resources, public water and wastewater treatment systems, and even human health. In this sense, it is essential to develop compact, easily automated, low-cost, and highly efficient unitary treatment processes in order to comply with legal requirements regarding effluent emission standards for water bodies. Therefore, the present study consisted of the development of two treatment processes aimed at the separation of oil emulsions stabilised by anionic surfactants: a sorption column using polyurethane/graphene foam composites as sorbent material and a continuous flow AC electroflotation reactor. Initially, composites with 0.5% and 1% w/w graphene (based on polyol mass) were developed using a dispersing agent (1-methyl-2-pyrrolidone). The foams were characterised in terms of morphology and mechanical and sorption properties. In the fixed bed column, the foams retained up to 77.15% of the emulsified oil and 52.36% of the anionic surfactants. In the continuous flow electroflotation reactor, emulsified oil removal efficiencies above 90% were achieved at all electrical currents tested, and up to 88.6% of anionic surfactants were removed at an electrical current of 150 A. Given the advantages and disadvantages of the two oily effluent treatment processes, their combined use in the same system proved promising.

The present study aims to evaluate thin plate-injected polypropylene (PP) composites containing short aramid fibers (AF) and graphene nanoplatelets (GNPs). The aramid fibers were manually cut to a length of 10 mm and added to the polypropylene matrix at a concentration of 10 wt.%. Additionally, GNPs were incorporated at concentrations of 0.1, 0.25, and 0.5 wt.%. Maleic anhydride grafted polypropylene (MAPP) was used at a concentration of 2 wt.% to improve the adhesion and compatibility between the polymer matrix and the fillers. Thermal analyses, tensile and flexural tests, and dynamic mechanical thermal analysis were performed, followed by statistical analysis using ANOVA and Tukey’s test. The composites demonstrated significant improvements in storage and loss moduli compared to neat polypropylene. With the addition of AF and GNPs, tensile strength increased to 46.8 MPa, which represents a 265% enhancement compared to PP. Similarly, flexural strength reached 62.4 MPa, significantly higher than the 36.73 MPa for PP, particularly for the composite containing AF and 0.25 wt.% GNPs. The results presented in this study highlight the synergistic effect of aramid fibers and GNPs on PP. These improvements make the proposed composites highly promising for a range of applications, including ballistic interlayered aramid/thin-plate laminates.

This research investigated the combination of acid functionalization and metal deposition on commercial activated carbon (AC) for the synthesis of electrodes for applications in supercapacitors. The effect of acid treatment and the deposition of metals, including nickel, copper, and cobalt on the electrochemical characteristics of the carbon material were assessed. The AC treatment with sulfuric acid resulted in a nearly twofold increase in surface area compared to the untreated AC, enhancing porosity and creating irregularities that improved the motion of ions and electrons, increasing the specific capacitance and energy density. Notably, we demonstrate that nickel deposition at only 2 wt% significantly improved specific capacitance (up to 59.58 F·g⁻¹), while preserving porosity and enhancing surface wettability. The adoption of a scalable, solvent-free, and low-energy technique for metal deposition on carbon structures presents promising opportunities for developing sustainable alternatives in energy storage technologies.