Recognition of sustainability issues around water resource consumption is gaining traction under global warming and land utilization complexities. These concerns increase the challenge of gaining an appropriate comprehension of the anthropogenic activities and natural processes, as well as how they influence the quality of surface water and groundwater systems. The characteristics of water resources cause difficulties in the comprehensive assessment regarding the source types, pathways, and pollutants behaviors. As the behavior and prediction of widely known contaminants in the water resources remain challenging, some new issues have developed regarding heavy metal pollutants. The main aim of this review is to focus on certain essential pollutants’ discharge from anthropogenic activities categorized based on land-use sectors such as industrial applications (solid/liquid wastes, chemical compounds, mining activities, spills, and leaks), urban development (municipal wastes, land use practices, and others), and agricultural practices (pesticides and fertilizers). Further, important pollutants released from natural processes classified based on climate change, natural disasters, geological factors, soil/matrix, and hyporheic exchange in the aquatic environment, are also discussed. Moreover, this study addresses the major inorganic substances (nitrogen, fluoride, and heavy metals concentrations). This study also emphasizes the necessity of transdisciplinary research and cross-border communication to achieve sustainable water quality using sound science, adaptable legislation, and management systems.

Although regarded as environmentally stable, bioelectrochemical fuel cells or, microbial fuel cells (MFCs) continue to face challenges with sustaining electron transport. In response, we examined the performance of two graphene composite-based anode electrodes—graphene oxide (GO) and GO–polymer–metal oxide (GO–PANI–Ag)—prepared from biomass and used in MFCs. Over 7 days of operation, GO energy efficiency peaked at 1.022 mW/m2 and GO–PANI–Ag at 2.09 mW/m2. We also tested how well the MFCs could remove heavy metal ions from synthetic wastewater, a secondary application of MFCs that offers considerable benefits. Overall, GO–PANI–Ag had a higher removal rate than GO, with 78.10% removal of Pb(II) and 80.25% removal of Cd(II). Material characterizations, electrochemical testing, and microbial testing conducted to validate the anodes performance confirmed that using new materials as electrodes in MFCs can be an attractive approach to improve the electron transportation. When used with a natural organic substrate (e.g., sugar cane juice), they also present fewer challenges. We also optimized different parameters to confirm the efficiency of the MFCs under various operating conditions. Considering those results, we discuss some lingering challenges and potential possibilities for MFCs.

Magnetic mesoporous silica nanoparticles (Fe3O4-MSNs) were successfully synthesized with a relatively high surface area of 568 m2g−1. Fe3O4-MSNs were then modified with poly(2-diethyl aminoethyl methacrylate) (PDEAEMA) brushes using surface-initiated ARGET atom transfer radical polymerization (ATRP) (Fe3O4@MSN-PDMAEMA). Since the charge of PDEAEMA is externally regulated by solution pH, tertiary amines in the polymer chains were quaternized using 2-iodoethanol to obtain cationic polymer chains with a permanent positive charge (Fe3O4@MSN-QPDMAEMA). The intensity of the C−O peak in the C1s X-ray photoelectron spectrum increased after reaction with 2-iodoethanol, suggesting that the quaternization process was successful. The applicability of the synthesized materials on the removal of methyl orange (MO), and sunset yellow (E110) dyes from an aqueous solution was examined. The effects of pH, contact time, and initial dyes concentrations on the removal performance were investigated by batch experiments. The results showed that the Fe3O4@MSN-PDMAEMA sample exhibited a weak adsorption performance toward both MO and E110, compared with Fe3O4@MSN-QPDMAEMA at a pH level above 5. The maximum adsorption capacities of MO and E110 using Fe3O4@MSN-QPDMAEMA were 294 mg g−1 and 194.8 mg g−1, respectively.

Microbial fuel cells (MFCs) are a sustainable approach for the remediation of metals and the simultaneous production of energy. This paper highlighted the usage of mango extract to produce electricity as an organic source for bacteria and reduce metal ions from wastewater. The observed results were 51 mV in 15 days with 500 Ω of external resistance. The whole operation was carried out at room temperature. The observed current and power density were 28.947 mA/m2 and 0.972 mW/m2, respectively. The internal resistance was 150 Ω, which is lower than external resistance. The remediation performance varied with the metal ions as follows: Pb (II) shows 75%, Cd (II) shows 74.11%, and Cr (III) shows 80.50%. Finally, the detailed working mechanism of the present study, MFC challenges, and future research directions are covered in this paper.

Background Virgin coconut oil is mostly made up of saturated fatty acids in which approximately 72% are medium chain triglycerides. Medium chain triglycerides can be digested into medium chain fatty acids and medium chain monoglycerides which are bioactive components. Therefore, it is very important to study the in-silico ability of some Virgin coconut oil derivatives, namely, medium chain fatty acids and medium chain monoglycerides to inhibit Cyclooxygenase 2 (COX-2) protein for prevention of excessive inflammatory response. Results Pharmacophore study displayed monolaurin with two hydrogen bond donor, three hydrogen bond acceptor and five hydrophobic interactions, while lauric acid presented two hydrogen bond acceptor, five hydrophobic interactions and a negative ion interaction. Molecular docking underlined the ability of monolaurin in the inhibition of COX-2 protein which causes inflammatory action with a decent result of energy binding affinity of − 7.58 kcal/mol and 15 interactions out of which 3 are strong hydrogen bond with TYR385 (3.00 Å), PHE529 (2.77 Å), and GLY533 (3.10 Å) residues of the protein. Monolaurin was employed as hydrogen bond acceptor to the side of residue TYR385 of COX-2 protein with an occupancy of 67.03% and was observed to be long-living during the entire 1000 frames of the molecular dynamic simulation. The analysis of RMSD score of the Monolaurin–COX-2 complex backbone was calculated to be low (1.137 $$\pm$$ ± 0.153 Å) and was in a stable range of 0.480 to 1.520 Å. Redocking of this complex still maintained a strong hydrogen bond (2.87 Å) with the main residue TYR385. AMDET results where promising for medium chain fatty acids and medium chain monoglycerides with good physicochemical drug scores. Conclusions This can be concluded from the results obtained that the monolaurin has strong interactions with COX-2 protein to disrupt its function due to significant hydrogen bonds and hydrophobic interactions with amino acid residues present in the target protein’s active site. These results displayed a very significant anti-inflammatory potential of monolaurin and a new promising drug candidates as anti-inflammatory agent. Graphical Abstract

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