Hydrothermally Synthesized rGO/MnO2/MoS2 Nanohybrids as Superior Bifunctional Electrocatalysts for Oxygen and Hydrogen Evolution Reactions.

This investigation delved into the field of bifunctional electrocatalyst water splitting, aimed at advancing sustainable energy by addressing the scarcity of efficient nonprecious electrocatalysts capable of facilitating both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). This study focused on nanohybrids consisting of hydrothermally synthesized rGO/MnO2/MoS2 composites and highlighted their efficacy as bifunctional electrocatalysts. The synergistic integration of rGO/MnO2/MoS2 enhanced the surface area, magnified electroactive sites, established a customized conductive arrangement, and provoked the efficiency in splitting of water. The nanohybrid displayed exceptional catalytic performance for the OER and HER, with significantly reduced overpotentials of 208 and 205 mV in 1 M KOH at 10 mA cm-2 current density, respectively. The findings underscore the potential of these cost-effective and environmentally friendly rGO/MnO2/MoS2 nanohybrids in advancing the field of electrocatalysis for renewable energy applications.

A review on recent advancements in the treatment of polyaromatic hydrocarbons (PAHs) using sulfate radicals based advanced oxidation process.

Polyaromatic hydrocarbons (PAHs) are the most persistent compounds that get contaminated in the soil and water. Nearly 16 PAHs was considered to be a very toxic according US protection Agency. Though its concentration level is low in the environments but the effects due to it, is enormous. Advanced Oxidation Process (AOP) is an emergent methodology towards treating such pollutants with low and high molecular weight of complex substances. In this study, sulfate radical (SO4‾•) based AOP is emphasized for purging PAH from different sources. This review essentially concentrated on the mechanism of SO4‾• for the remediation of pollutants from different sources and the effects caused due to these pollutants in the environment was reduced by this mechanism is revealed in this review. It also talks about the SO4‾• precursors like Peroxymonosulfate (PMS) and Persulfate (PS) and their active participation in treating the different sources of toxic pollutants. Though PS and PMS is used for removing different contaminants, the degradation of PAH due to SO4‾• was presented particularly. The hydroxyl radical (•OH) mechanism-based methods are also emphasized in this review along with their limitations. In addition to that, different activation methods of PS and PMS were discussed which highlighted the performance of transition metals in activation. Also this review opened up about the degradation efficiency of contaminants, which was mostly higher than 90% where transition metals were used for activation. Especially, on usage of nanoparticles even 100% of degradation could be able to achieve was clearly showed in this literature study. This study mainly proposed the treatment of PAH present in the soil and water using SO4‾• with different activation methodologies. Particularly, it emphasized about the importance of treating the PAH to overcome the risk associated with the environment and humans due to its contamination.

Design of biocompatible gelatin hydrogels reinforced with magnetite nanoparticles: Effective removal of chromium from water environment.

The development of biocompatible adsorbents is vital for environmental remediation to control and reduce pollution and waste accumulation in ecosystems. Biocompatible hydrogels represent an innovative class of materials that are primarily composed of polymer chain units forming their structural framework. They have a high affinity for water molecules. This research thus aims to incorporate iron oxide particles into the gelatin matrix to produce gelatin hydrogel beads to remove hexavalent chromium from an aqueous solution. The synthesized beads, known for their consistent size, low friction, high specific surface area, mechanical stability, and lightweight characteristics, demonstrated their suitability for various industrial applications. The effectiveness of these hydrogels in removing hexavalent chromium ions was confirmed through a thorough analysis using techniques such as FTIR, TGA, SEM, EDX, VSM, and XPS. Batch experiments revealed that the gelatin-based nanocomposite beads exhibited optimal adsorption efficiency under acidic conditions, lower initial concentrations of chromium ions, extended contact time, and elevated temperature (50-60 °C). The composite achieved a maximum removal efficiency of 99% at pH 1, with an adsorbent dose of 0.5 g at 50 °C, and an initial concentration of 50 mg per liter. The use of 0.7 N NaOH in the regeneration process resulted in a commendable 70.5% desorption efficiency, enabling potential reuse and regeneration. Significantly, the desorption efficiency remained consistently high even after four desorption-readsorption cycles, contributing to the economic and environmental sustainability of chromium removal. Additionally, the study determined that the sorption process was feasible, spontaneous, and endothermic. These collective findings suggest that magnetic gelatin hydrogel beads could serve as a cost-effective alternative adsorbent for the efficient removal of chromium ions from aqueous solutions.

Effective removal of chromium by adsorption using Delonix regia bark derived activated carbon from aqueous solution: a sustainable approach.

This study introduces a new biosorbent derived from Delonix regia bark-activated carbon to efficiently remove Chromium Cr(VI) metal ions from aqueous systems. The biosorbent was synthesized from the bark powder of the plant species and chemically activated with phosphoric acid. The biosorbent was characterized using FTIR, SEM, and BET to determine its functional properties and structural morphology. The batch adsorption experiments examined the optimal conditions for Cr(VI) metal ion adsorption, identifying that the highest removal efficiency occurred at pH levels of 2. The ideal adsorbent dosage was determined to be 2.5 g/L, with equilibrium achieved at a contact time of 60 min at the optimal temperature of about 303 K for a Cr(VI) metal ion concentration of 20 mg/L. Various isotherm models were applied to the adsorption equilibrium values, revealing that the adsorbent had a maximum removal capacity of approximately 224.8 mg/g for Cr(VI) metal ions. The adsorption process of Cr(VI) on the DAC biosorbent was best described by the Freundlich isotherm, indicating multilayer adsorption. The kinetic data fit well with the pseudo-second-order model. Thermodynamic parameters suggested that the adsorption process was spontaneous, exothermic, and feasible across different temperatures. Furthermore, the desorption studies showed that the DAC biosorbent can easily be rejuvenated and utilized several cycles with high adsorption capacity. These findings indicate that the developed adsorbent is environmentally friendly and effective for removing Cr(VI) from water systems.

A critical review on biochar for the removal of toxic pollutants from water environment.

As an effort to tackle some of the most pressing ecological issues we are currently experiencing, there has been an increasing interest in employing biomass-derived char products in various disciplines. Thermal combustion of biomass results in biochar production, which is a remarkably rich source of carbon. Not only does the biochar obtained by the thermochemical breakdown of biomass lower the quantity of carbon released into the environment, but it also serves as an eco-friendly substitute for activated carbon (AC) and further carbon-containing products. An overview of using biochar to remove toxic pollutants is the main subject of this article. Several techniques for producing biochar have been explored. The most popular processes for producing biochar are hydrothermal carbonization, gasification and pyrolysis. Carbonaceous materials, alkali, acid and steam are all capable of altering biochar. Depending on the environmental domains of applications, several modification techniques are chosen. The current findings on characterization and potential applications of biochar are compiled in this survey. Comprehensive discussion is given on the fundamentals regarding the formation of biochar. Process variables influencing the yield of biochar have been summarized. Several biochars' adsorption capabilities for expulsion pollutants under various operating circumstances are compiled. In the domain of developing biochar, a few suggestions for future study have been given.

Fluorescence enhancing and quenching signal based on new approach for selective detection of multiple organochlorine pesticides using blue emissive-carbon dot.

Measuring the concentration of organochlorine pesticides (OCPs) in agriculture has engaged significant awareness for healthcare investigation since OCPs are harmful to many physiological processes. Excessive usage of these compounds can result in major contamination of the environment and food supply chains. As a result, more accurate and rapid ways to detect pesticide residues in food are required. In this work, we have portrayed the surface-engineered fluorescent blue emissive-carbon dot (B-CD) with a high quantum yield (49.3 %) via the hydrothermal method for fluorescent sensing of OCPs on real samples. The amine group functionalities of carbon dots have supported the direct coordination with -Cl and -OH groups of HEP, ENS, CDF and 2,4-DPAC for the sensitive detection of OCPs, by switching in the fluorescent intensity of B-CD. The functional group of OCPs exhibits a variety of binding interactions with B-CD to contribute a complex formation, which leads to static quenching via an insubstantial restricted electron transfer process. The synthesized carbon dots exhibit individuality in binding nature towards different OCPs. Fluorescence studies help to distinguish the target OCPs and their low detection limits (LODs) were 0.002, 0.099, 0.16 and 0.082 µM for Heptachlor (HEP - turn "on"), Endosulfan (ENS), Chlordimeform (CDF) and 2,4-dichlorophenoxyacetic acid (2,4-DPAC - turn "off") OCPs respectively. The real water samples and agriculture food samples were effectively investigated and the OCP toxicity was noted. Thus, the design of the fluorescence sensor is established as an easy and proficient sensing method for detecting OCPs.

Fungal bioremediation approaches for the removal of toxic pollutants: Mechanistic understanding for biorefinery applications.

Pollution is a global menace that poses harmful effects on all the living ecosystems and to the Earth. As years pass by, the available and the looming rate of pollutants increases at a faster rate. Although many treatments and processing strategies are waged for treating such pollutants, the by-products and the wastes or drain off generated by these treatments further engages in the emission of hazardous waste. Innovative and long-lasting solutions are required to address the urgent global issue of hazardous pollutant remediation from contaminated environments. Myco-remediation is a top-down green and eco-friendly tool for pollution management. It is a cost-effective and safer practice of converting pernicious substances into non-toxic forms by the use of fungi. But these pollutants can be transformed into useable products along with multiple benefits for the environment such as sequestration of carbon emissions and also to generate high valuable bioactive materials that fits as a sustainable economic model. The current study has examined the possible applications of fungi in biorefineries and their critical role in the transformation and detoxification of pollutants. The paper offers important insights into using fungal bioremediation for both economically and environmentally sound solutions in the domain of biorefinery applications by combining recent research findings.