Enhanced membraneless fuel cells by electrooxidation of ethylene glycol with a nanostructured cobalt metal catalyst.

The advancement of effective and long-lasting electrocatalysts for energy storage devices is crucial to reduce the impact of the energy crisis. In this study, a two-stage reduction process was used to synthesize carbon-supported cobalt alloy nanocatalysts with varying atomic ratios of cobalt, nickel and iron. The formed alloy nanocatalysts were investigated using energy-dispersive X-ray spectroscopy, X-ray diffraction, and transmission electron microscopy to determine their physicochemical characterization. According to XRD results, Cobalt-based alloy nanocatalysts form a face-centered cubic solid solution pattern, illustrating thoroughly mixed ternary metal solid solutions. Transmission electron micrographs also demonstrated that samples of carbon-based cobalt alloys displayed homogeneous dispersion at particle sizes ranging from 18 to 37 nm. Measurements of cyclic voltammetry, linear sweep voltammetry, and chronoamperometry revealed that iron alloy samples exhibited much greater electrochemical activity than non-iron alloy samples. The alloy nanocatalysts were evaluated as anodes for the electrooxidation of ethylene glycol in a single membraneless fuel cell to assess their robustness and efficiency at ambient temperature. Remarkably, in line with the results of cyclic voltammetry and chronoamperometry, the single-cell test showed that the ternary anode works better than its counterparts. The significantly higher electrochemical activity was observed for alloy nanocatalysts containing iron than for non-iron alloy catalysts. Iron stimulates nickel sites to oxidize cobalt to cobalt oxyhydroxides at lower over-potentials, which contributes to the improved performance of ternary alloy catalysts containing iron.

Process optimization of struvite recovered from slaughterhouse wastewater and its fertilizing efficacy in amendment of biofertilizer.

The intensive discharge of slaughterhouse waste into water bodies increases Nitrogen (N), Phosphorus (P) in the wastewater and leads to various environmental problems. On the other hand, the increasing treatment effort after the extraction of these valuable nutrients in the commercial fertilizer reduces the dependence on scarce phosphate resources. The viable solution is to recover N, P as struvite (magnesium ammonium phosphate) from nutrient rich waste water as a small scale treatment unit application. The main parameters that have a significant impact on the process, including pH, Mg: P ratio, and precipitation time, were investigated from slaughterhouse wastewater using a central composite design and the experimental data's were statistically analysed. The results indicated that pH and Mg/P ratio level had a significant impact and thus 85% struvite precipitation efficiency was achieved at 9.6 pH and 1.5 dose mol ratio (mol Mg per mol P), in an inexpensive, stirred tank batch reactor with a retention time of 70 min. The fertilization efficiency was tested on the growth of Solanum melongena L with the obtained struvite and the integration of struvite with the Azospirullum rhizobium and Bacillus megaterium. Treatment of struvite, struvite with Azospirillum rhizobium and Bacillus megaterium increased growth parameters by 10%, 20%, and 25%, respectively, over control. The assessment of growth factors showed the most amazing number of fruits, shoots, and root length in a standard ratio of 60:40 of struvite to bio-inoculants compared to sole struvite fertilizer. Findings of this study would be beneficial to determine the feasibility of slaughterhouse waste as a phosphorus source for struvite recovery.