Microbial electrosynthesis: carbonaceous electrode materials for CO2 conversion.

Microbial electrosynthesis (MES) is a sustainable approach to address greenhouse gas (GHG) emissions using anthropogenic carbon dioxide (CO2) as a building block to create clean fuels and highly valuable chemicals. The efficiency of MES-based CO2 conversion is closely related to the performance of electrode material and, in particular, the cathode for which carbonaceous materials are frequently used. Compared to expensive metal electrodes, carbonaceous materials are biocompatible with a high specific surface area, wide range of possible morphologies, and excellent chemical stability, and their use can maximize the growth of bacteria and enhance electron transfer rates. Examples include MES cathodes based on carbon nanotubes, graphene, graphene oxide, graphite, graphite felt, graphitic carbon nitride (g-C3N4), activated carbon, carbon felt, carbon dots, carbon fibers, carbon brushes, carbon cloth, reticulated vitreous carbon foam, MXenes, and biochar. Herein, we review the state-of-the-art MES, including thermodynamic and kinetic processes that underpin MES-based CO2 conversion, as well as the impact of reactor type and configuration, selection of biocompatible electrolytes, product selectivity, and the use of novel methods for stimulating biomass accumulation. Specific emphasis is placed on carbonaceous electrode materials, their 3D bioprinting and surface features, and the use of waste-derived carbon or biochar as an outstanding material for further improving the environmental conditions of CO2 conversion using carbon-hungry microbes and as a step toward the circular economy. MES would be an outstanding technique to develop rocket fuels and bioderived products using CO2 in the atmosphere for the Mars mission.

Antioxidant, Anti-Bacterial, and Congo Red Dye Degradation Activity of AgxO-Decorated Mustard Oil-Derived rGO Nanocomposites.

Scaling up the production of functional reduced graphene oxide (rGO) and its composites requires the use of low-cost, simple, and sustainable synthesis methods, and renewable feedstocks. In this study, silver oxide-decorated rGO (AgxO-rGO) composites were prepared by open-air combustion of mustard oil, essential oil-containing cooking oil commercially produced from the seeds of Brassica juncea. Silver oxide (AgxO) nanoparticles (NPs) were synthesized using Coleus aromaticus leaf extract as a reducing agent. Formation of mustard seed rGO and AgxO NPs was confirmed by UV-visible characteristic peaks at 258 nm and 444 nm, respectively. rGO had a flake-like morphology and a crystalline structure, with Raman spectra showing clear D and G bands with an ID/IG ratio of 0.992, confirming the fewer defects in the as-prepared mustard oil-derived rGO (M-rGO). The rGO-AgxO composite showed a degradation efficiency of 81.9% with a rate constant k-1 of 0.9506 min-1 for the sodium salt of benzidinediazo-bis-1-naphthylamine-4-sulfonic acid (known as the azo dye Congo Red) in an aqueous solution under visible light irradiation. The composite also showed some antimicrobial activity against Klebsilla pneomoniae, Escherichiacoli, and Staphylococcusaureus bacterial cells, with inhibition zones of ~15, 18, and 14 mm, respectively, for a concentration of 300 µg/mL. At 600 µg/mL concentration, the composite also showed moderate scavenging activity for 2,2-diphenyl-1-picrylhydrazyl of ~30.6%, with significantly lower activities measured for AgxO (at ~18.1%) and rGO (~8%) when compared to control.

Multifunctional oil-produced reduced graphene oxide - Silver oxide composites with photocatalytic, antioxidant, and antibacterial activities.

Graphene-based nanomaterials that combine significant photocatalytic, antioxidant and antibacterial activity are very attractive candidates for biomedical and environmental applications. Conventional chemical synthesis routes may contaminate the resultant materials with toxic molecules, compromising their properties and limiting their use in biomedical applications. Ideally, to avoid any contamination, the nanomaterials should be synthesized from non-toxic precursors and reagents, e.g. foodstuff via a simple technology that does not rely on the use of hazardous chemicals yet produces materials of high quality. Here, we report an environmentally friendly, low cost reduced graphene oxide-silver-silver oxide nanocomposite with strong photocatalytic, antioxidant and antibacterial activity for environmental remediation. The reduced graphene oxide (FRGO) is synthesized from edible sunflower oil via a simple flame synthesis method. Next, silver nanoparticles (Ag/AgO/Ag2O) are produced by phytochemical reduction of AgNO3 using a reducing agent based on flavonoids from Coleus aromaticus (Mexican mint), also used in food industry. Thus-obtained FRGO-Ag/AgO/Ag2O composite is characterized using X-ray diffraction spectroscopy, scanning electron microscopy, fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy. The degradation of anionic textile dye Methylene blue (MB) is used as a measure of photocatalytic activity of FRGO and FRGO/Ag/AgO/Ag2O, with solution pH, initial dye concentration, and quantity of the catalyst considered as influencing factors. FRGO-Ag/AgO/Ag2O composites show strong antioxidant activity, with improved radical inhibition as well as dye degradation properties when compared to pristine FRGO.

Synthesis and characterization of amidoxime modified chitosan/bentonite composite for the adsorptive removal and recovery of uranium from seawater.

A novel amidoxime functionalized adsorbent, poly(amidoxime)-grafted-chitosan/bentonite composite [P(AO)-g-CTS/BT] was prepared by in situ intercalative polymerization of acrylonitrile (AN) and 3-hexenedinitrile (3-HDN) onto chitosan/bentonite composite using ethylene glycol dimethacrylate (EGDMA) as cross linking agent and potassium peroxy disulphate (K2S2O8) as free radical initiator. The adsorbent was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Scanning electron microscopy (SEM), Energy dispersive spectroscopy (EDS), BET surface area analyser and X-ray photoelectron spectroscopy (XPS). Nitrile groups from two monomers converted to amidoxime groups and therefore, increases the adsorption efficiency of uranium(VI) [U(VI)] from seawater. The optimum pH for U(VI) adsorption was found to be 8.0. The adsorbent dosage of 2.0 g/L was sufficient for the complete removal of U(VI) from seawater. The kinetic data fitted well with pseudo-second-order kinetic model which assumes the presence of chemisorption. The equilibrium attained within 60 min and well agreement of equilibrium data with Langmuir adsorption model confirms monolayer coverage of U(VI) onto P(AO)-g-CTS/BT. The maximum adsorption capacity was found to be 49.09 mg/g. Spent adsorbent was effectively regenerated using 0.1 N HCl. Six cycles of adsorption-desorption experiments were conducted to study the practical applicability and repeated use of the adsorbent. The feasibility of the adsorbent was also tested using natural seawater. The results show that P(AO)-g-CTS/BT is a promising adsorbent for the removal of U(VI) from seawater.

Synergic bactericidal effects of reduced graphene oxide and silver nanoparticles against Gram-positive and Gram-negative bacteria.

Reduced graphene oxide (rGO) is a promising antibacterial material, the efficacy of which can be further enhanced by the addition of silver nanoparticles (nAg). In this study, the mechanisms of antibacterial activity of rGO-nAg nanocomposite against several important human pathogenic multi-drug resistant bacteria, namely Gram-positive coccal Staphylococcus aureus and Gram-negative rod-shaped Escherichia coli and Proteus mirabilis are investigated. At the same concentration (100 µg/ml), rGO-nAg nanocomposite was significantly more effective against all three pathogens than either rGO or nAg. The nanocomposite was equally active against P. mirabilis and S. aureus as systemic antibiotic nitrofurantoin, and significantly more effective against E. coli. Importantly, the inhibition was much faster in the case of rGO-nAg nanocomposite compared to nitrofurantoin, attributed to the synergistic effects of rGO-nAg mediated contact killing and oxidative stress. This study may provide new insights for the better understanding of antibacterial actions of rGO-nAg nanocomposite and for the better designing of graphene-based antibiotics or other biomedical applications.