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Aquatic ecosystems and potable water are being exploited and depleted due to urbanization and the encouragement of extensive industrialization, which induces the scarcity of pure water. However, current decontamination methods are limited and inefficient. Various innovative remediation strategies with novel nanomaterials have recently been demonstrated for wastewater treatment. Carbon dots (C-dots) and graphene quantum dots (GQ-dots) are the most recent frontiers in carbon nanomaterial-based adsorption studies. C-dots are extremely small (1–10 nm) quasi-spherical carbon nanoparticles (mostly sp3 hybridized carbon), whereas GQ-dots are fragments of graphene (1–20 nm) composed of primarily sp2 hybridized carbon. This article highlights the function of C-dots and GQ-dots with their specifications and characteristics for the efficient removal of organic and inorganic contaminants in water via adsorption chromatography. The alteration of adsorption attributes with the hybrid blending of these dots has been critically analyzed. Moreover, various top-down and bottom-up approaches for synthesizing C-dots and GQ-dots, which ultimately affect their morphology and structure, are described in detail. Finally, we review the research deficit in the adsorption of diverse pollutants, fabrication challenges, low molecular weight, self-agglomeration, and the future of the dots by providing research prospects and selectivity and sensitivity perspectives, the importance of post-adsorption optimization strategies and the path toward scalability at the tail of the article. [ABSTRACT FROM AUTHOR]

The contamination of water with organic pollutants such as dyes and phenols is a serious environmental problem, requiring effective treatment methods. In the present study, a novel nanocomposite was synthesized by intercalating graphene oxide and bentonite clay into MgFeAl-layered triple hydroxide (GO/BENT/LTH), which was characterized using different techniques. The adsorption efficacy of the GO/BENT/LTH nanocomposite was assessed via the removal of two harmful organic water pollutants, namely methyl orange (MO) and 2-nitrophenol (2NP). The obtained results revealed that the maximum adsorption capacities (q max) of MO and 2NP reached 3106.3 and 2063.5 mg/g, respectively, demonstrating the excellent adsorption performance of the nanocomposite. Furthermore, this study examined the effects of contact time, initial MO and 2NP concentrations, pH, and temperature of the wastewater samples on the adsorptive removal of MO and 2NP by the GO/BENT/LTH nanocomposite. The pH, zeta potential, and FTIR investigations suggested the presence of more than one adsorption mechanism. Thermodynamic investigations elucidated the exothermic nature of the adsorption of MO and 2NP onto the GO/BENT/LTH nanocomposite, with MO adsorption being more sensitive to temperature change. Additionally, regeneration studies revealed a marginal loss in the MO and 2NP removal with the repetitive use of the GO/BENT/LTH nanocomposite, demonstrating its reusability. Overall, the findings of this study reveal the promise of the GO/BENT/LTH nanocomposite for effective water decontamination. • Novel GO/clay/MgFeAl-LTH nanocomposites is synthesized and characterized herein. • The nanocomposite outperformed its parental materials and their binary combinations. • The q max of MO and 2NP using this nanocomposite are >3000 and > 2000 mg/g, respectively. • Both pollutants adsorb spontaneously and exothermically on the nanocomposite. • The nanocomposite can be used multiple times with insignificant performance loss. [ABSTRACT FROM AUTHOR]

The excessive and uncontrollable discharge of diverse organic pollutants into the environment has emerged as a significant concern, presenting a substantial risk to human health. Among the advanced oxidation processes used for the purification of wastewater, cold plasma technology is superior in fast and effective decontamination but often fails facing mixed pollutants. To address these issues, here we develop the new conceptual approach, plasma process, and proprietary reactor that ensure, for the first time, that the efficiency of treatment (114.7%) of two mixed organic dyes, methylene blue (MB) and methyl orange (MO), is higher than when the two dyes are treated separately. We further reveal the underlying mechanisms for the energy-efficient complete degradation of the mixed dyes. The contribution of plasma-induced ROS and the distinct degradation characteristics and mechanism of pollutants in mixed treatment are discussed. The electron transfer pathway revealed for the first time suggest that the mixed pollutants reduce the overall redox potentials and facilitate electron transfer during the plasma treatment, promoting synergistic degradation effects. The integrated frameworks including both direct and indirect mechanisms provide new insights into the high-efficiency mixed-contaminant treatment. The degradation products for mixed degradation are revealed based on the identification of intermediate species. The plasma-treated water is proven safe for living creatures in waterways and sustainable fishery applications, using in vivo zebrafish model bio-toxicity assay. Overall, these findings offer a feasible approach and new insights into the mechanisms for the development of highly-effective, energy-efficient technologies for wastewater treatment and reuse in agriculture, industry, and potentially in urban water networks. [Display omitted] • The mixed treatment exhibited significant efficiency improvements (114.7%) than the separate treatment. • Unveiled synergistic ROS and electron transfer mechanism during plasma treatment. • Confirmed treated solution's biosafety via in vivo zebrafish tests and ECOSAR model. • Results offer data and theory for feasible engineering applications. [ABSTRACT FROM AUTHOR]