AppliedChem

This study explores, for the first time, the bioaccumulation of americium-241 (²⁴¹Am) by Cupriavidus metallidurans and Ochrobactrum anthropi, two bacterial strains previously investigated mainly for their interactions with other heavy metals and radionuclides. To the best of our knowledge, no prior studies have reported the use of these microorganisms for ²⁴¹Am removal from aqueous solutions. The effects of initial ²⁴¹Am concentration and solution pH on removal performance were evaluated through batch experiments. Kinetic analyses were performed using pseudo-first-order (PFO) and pseudo-second-order (PSO) models, with the PSO model providing a better fit, suggesting chemisorption as the rate-limiting step in the process. Initial ²⁴¹Am concentrations ranged from 75 to 300 Bq mL⁻¹, and both bacterial strains demonstrated comparable maximum bioaccumulation capacities of approximately 1.5 × 10⁻⁸ mmol g⁻¹. However, O. anthropi exhibited superior resistance to ²⁴¹Am, maintaining colony growth at activity levels up to 1200 Bq mL⁻¹, compared to a threshold of 400 Bq mL⁻¹ for C. metallidurans. These findings highlight the robustness and efficiency of these bacterial strains—particularly O. anthropic—in removing ²⁴¹Am from liquid radioactive waste, offering promising implications for bioremediation technologies.

Lithium-ion batteries (LIBs) are vital for modern energy storage applications. Lithium iron phosphate (LFP) is a promising cathode material due to its safety, low cost, and environmental friendliness compared to the widely used nickel manganese cobalt oxide (NMC), which contains hazardous nickel and cobalt compounds. However, challenges remain in enhancing the performance of LFP cathodes due to their low electronic and ionic conductivity. To improve both the safety and sustainability of the battery, this work presents a water-based LFP cathode utilizing the bio-based binder carboxymethyl cellulose (CMC), eliminating the need for polyvinylidene fluoride (PVDF) and the toxic solvent N-methyl-2-pyrrolidone (NMP). This study investigates the impact of different dispersing methods—dissolver mixing and wet jet milling—on slurry properties, electrode morphology, and battery performance. Slurries were characterized by rheology, particle size distribution, and sedimentation behavior, while coated and calendered electrodes were examined via thickness measurements and scanning electron microscopy (SEM). Electrochemical performance of the electrodes was evaluated by means of C-Rate testing. The results reveal that dispersing methods significantly influence slurry characteristics but marginally affect electrochemical performance. Compared to dissolver mixing, wet jet milling reduced the median particle size by 39% (ΔD50 = 3.1 µm) and lowered viscosity by 96% at 1 s⁻¹, 80% at 105 s⁻¹, and 64% at 1000 s⁻¹. In contrast, the electrochemical performance of the resulting electrodes differed only slightly, with discharge capacity varying by approximately 12.8% at 1.0 C (Δcapacity = 10.7 mAh g⁻¹). This research highlights the importance of optimizing not only material selection but also processing techniques to advance safer and more sustainable energy storage solutions.

The presence of 2-methylisoborneol (2-MIB) in water is a critical global concern due to its low threshold and resistance to conventional processes. In the present study, activated carbon/alginate (AC/alginate) composite beads were synthesized via ionic gelation method for the removal of 2-MIB from aqueous solution. The physicochemical characteristics of the adsorbent were determined using scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) techniques. The effects of contact time, solution pH, initial 2-MIB concentration and adsorbent dose on adsorption were examined. Over 95% of 2-MIB removal was obtained under optimum conditions within 360 min. The adsorption equilibrium was well described by Langmuir (R² = 0.97) and Freundlich (R² = 0.96) models suggesting that 2-MIB adsorption involves both monolayer and multilayer adsorption. Kinetic modeling revealed that the pseudo-first order model showed strong fits to the experimental data, indicating the role of surface adsorption in controlling the rate of adsorption. The adsorbent demonstrated reasonable stability, retaining 59% removal efficiency after four adsorption–desorption cycles, highlighting its potential for repeated application in water treatment. Overall, the AC/alginate composite beads were found to be promising for the effective elimination of 2-MIB from water.