Magnetic nanoparticles are used in adsorptive removal of heavy metals from polluted wastewater. However, their poor stability in an acidic medium necessitates their protection with a coating layer. Coating magnetic nanoparticles with carbon showed proper protection but the heavy metal removal efficiency was slightly weak. However, to boost the removal efficiencies of surface functionalization, polyacrylamide was applied to carbon-coated Fe₃O₄ nanoparticles. In this paper, to facilitate the synthesis process, one-step carbon coating and polyacrylamide functionalization were conducted using the hydrothermal technique with the aim of enhancing the adsorptive removal capacity of Fe₃O₄ nanoparticles towards some heavy metals such as Cu(II), Ni(II), Co(II), and Cd(II). The results showed that the one-step process succeeded in developing a carbon coating layer and polyacrylamide functionality on Fe₃O₄ nanoparticles. The stability of the magnetic Fe₃O₄ nanoparticles as an adsorbent in an acidic medium was improved due to its resistance to the dissolution that was gained during carbon coating and surface functionalization with polyacrylamide. The adsorptive removal process was investigated in relation to various parameters such as pH, time of contact, metal ion concentrations, adsorbent dose, and temperature. The polyacrylamide functionalized Fe₃O₄ showed an improvement in the adsorption capacity as compared with the unfunctionalized one. The conditions for superior adsorption were obtained at pH 6; time of contact, 90 min; metal solution concentration, 200 mg/L; adsorbent dose, 0.3 g/L. The modeling of the adsorption data was found to be consistent with the pseudo-second-order kinetic model, which suggests a fast adsorption process. However, the equilibrium data modeling was consistent with both the Langmuir and Freundlich isotherms. Furthermore, the thermodynamic parameters of the adsorptive removal process, including ΔG°, ΔH°, and ΔS°, indicated a spontaneous and endothermic sorption process. The developed adsorbent can be utilized further for industrial-based applications.

The contamination of water surfaces by mercury is a dangerous environmental problem due to its toxicity, which leads kidney damage. Activated carbon from mixed recyclable waste modified by phosphonium-based ionic liquid (IL-ACMRW) was therefore prepared and evaluated for Hg(II) remediation. The activated carbon used in this study was prepared from mixed waste, including cardboard, papers and palm wastes as cheap raw materials. The mixed Recyclable Waste Activated Carbon was combined with trihexyl(tetradecyl)phosphonium Bis2,4,4-(trimethylpentyl)phosphinate (Cyphos^® IL 104) ionic liquid to form an adsorbent with organic-inorganic content, in order to improve the Hg(II) uptake from aqueous solutions. FTIR confirms the presence of P, C=O and OH after this modification. The adsorption process was investigated and the evaluated results showed that the capacity was 124 mg/g at pH 4, with a contact time of 90 min, an adsorbent dose of 0.4 g/L, and a Hg(II) concentration of 50 mg/L. This Hg(II) adsorption capacity is superior than that reported in the literature for modified multiwall carbon nanotubes. The adsorption of Hg(II) on the modified activated carbon from mixed recyclable waste was found to follow the pseudo second-order kinetics model. Isotherms of adsorption were analyzed via Freundlich and Langmuir models. The results indicated that Freundlich is the best model to describe the process, suggesting multilayer adsorption.

The discharge of pharma products such as paracetamol (PCT) into water has resulted in great harm to humans and emerged as a potential threat requiring a solution. Therefore, the development of smart and efficient materials as photocatalysts has become imperative in order to treat PCT in wastewater. The present study demonstrates the synthesis of pristine NiWO₄ and CoWO₄ and a heterojunction nanostructure, NiWO₄/CoWO₄, through a hydrothermal process using a Teflon-lined autoclave at 180 °C for 18 h. Various spectroscopic techniques, such as X-ray diffraction (XRD), Fourier transform infrared (FTIR), ultraviolet–visible (UV–Vis), transmission electron microscopy (TEM), scanning electron microscopy–energy dispersive X-ray (SEM–EDX), and X-ray photoelectron spectroscopy (XPS) were utilised to determine the lattice, structural, optical, and morphological information of the solid nanomaterial upon heterojunction formation. The synthesised nanomaterials were exploited for the photocatalytic degradation of paracetamol (PCT) under UV light irradiation. Photocatalytic experiments were performed for the optimization of various reaction parameters, such as irradiation time, pH, catalyst dose, and PCT concentration at room temperature. The results obtained suggested that the heterojunction nanocomposite NiWO₄/CoWO₄ exhibited enhanced photocatalytic efficiency (97.42%) with PCT as compared to its precursors—96.50% for NiWO₄ and 97.12% for CoWO₄. The photocatalytic data were best defined by the Langmuir–Hinshelwood (L–H) model of pseudo-first-order kinetics, with apparent rates constant at 0.015 min⁻¹ for NiWO₄, 0.017 min⁻¹ for CoWO₄, and 0.019 min⁻¹ for NiWO₄/CoWO₄ NC. It was observed that NiWO₄/CoWO₄ NC with enhanced optical properties effected a higher rate of PCT degradation due to the improved bandgap energy upon heterojunction formation. The scavenger test revealed the involvement of ^•OH radicals as reactive oxidant species (ROS) in PCT degradation. The material was found to be highly stable and reusable for the degradation of PCT at optimized reaction conditions.

In this work, metal organic frameworks (A100 Al-based MOFs) were used in dispersive solid-phase microextraction (DSPME) for the isolation and preconcentration of the carbaryl from vegetable, fruit and water samples. The A100 Al-based MOFs showed excellent behavior for the adsorption of carbaryl from a water–ethanol solution; additionally, carbaryl was easily desorbed with ethyl acetate for detection by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-TMS). The analytical process of DSPME together with UPLC-TMS provides the accurate monitoring of trace carbaryl residues. The results show that the optimal recovery% of carbaryl was obtained at a sample apparent pH of 5, with the application of 1 mL of ethyl acetate to elute the carbaryl from the A100 Al-based MOFs. The limit of detection (LOD) and the limit of quantification (LOQ) were 0.01 mg.L⁻¹ and 0.03 mg.L⁻¹, respectively. The RSD% was 0.8–1.9, and the preconcentration factor was 45. DSPME and UPLC-TMS were successfully used for the isolation and detection of carbaryl in food and water samples.

The innovation and development of water purification methods have been at the center of extensive research for several decades. Many nanoparticles are frequently seen in industrial waste water. In this research, zinc oxide nanoparticles (ZnO) were synthesized following an autocombustion method with and without honey capping. Structural crystallinity and bonding structure were examined via X-ray diffraction (XRD) analysis and Fourier transform infrared (FTIR) spectroscopy. Optical behavior was analyzed using ultraviolet–visible (UV–Vis) spectroscopy and photoluminescence (PL). Size estimation and surface morphology were studied using scanning electron microscopy (SEM), while energy-dispersive spectroscopy (EDS) was performed to analyze the sample purity and elemental composition. The photocatalytic degradation of methylene blue (MB) by ZnO was assessed as it is an efficient water treatment process with high potential. The biological activity of ZnO nanoparticles was also investigated in terms of antibacterial and antifungal activities against different bacterial and fungal species. Surprisingly, the as-synthesized ZnO nanoparticles were found to be substantially bioactive compared to conventional drugs. Honey-mediated nanoparticles displayed 86% dye degradation efficiency, and that of bare ZnO was 60%. Therefore, the involvement of honey in the synthesis of ZnO nanoparticles has great potential due to its dual applicability in both biological and environmental remediation processes.

Construction of a homojunction is an effective strategy for effective charge transfer to suppress charge carrier recombination in augmented photocatalysis. The present work reveals the synthesis of homojunction formation through the reinforcement of Cd nanostructures into a solid lattice of zinc vanadate (Zn₃V₂O₈, ZnV) using the hydrothermal method. The formation of a homojunction between cadmium vanadate (CdV, Cd₃V₂O₈) and ZnV was confirmed by various spectroscopic and electron microscopic techniques such as Fourier-transform infrared (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) associated with energy-dispersive X-ray (EDX) mapping, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and ultraviolet–visible spectrophotometry (UV–Vis). The synthesized material was explored for photocatalytic hydrogen (PC H₂) production using the water splitting process under visible-light illumination. The spectroscopic and experimental results revealed that the formation of a CdV/ZnV homojunction significantly improved the transport of photogenerated charge carriers (electron–hole pairs) and thus resulted in enhanced H₂ production efficiency (366.34 μmol g⁻¹ h⁻¹) as compared to pristine ZnV (229.09 μmol g⁻¹ h⁻¹) and CdV (274.91 μmol g⁻¹ h⁻¹) using methanol as a sacrificial reagent (SR) with water under visible-light illumination. The synergistic effect of Cd on ZnV NPs resulted in band gap reduction and broadened visible light absorption which was attributed to enhanced H₂ production. The current study explains how a homojunction affects various features of important factors behind photocatalytic activity, which supports significant insights into the advancement of materials in the future.