In this study, zinc vanadate/reduced graphene oxide (Zn3V2O8/rGO) composite has been synthesized via a simple approach. Advanced characterization techniques (powder X-ray, scanning electron microscopy, energy dispersive X-ray spectroscopy and ultraviolet-visible (UV-vis) spectroscopy) have been used to authenticate the formation of Zn3V2O8/rGO composite. Subsequently, Zn3V2O8/rGO was applied as photo-catalyst for hydrogen generation using photo-catalysis. The Zn3V2O8/rGO photo-catalyst exhibited a good hydrogen generation amount of 104.6 µmolg−1. The Zn3V2O8/rGO composite also demonstrates excellent cyclic stability which indicated better reusability of the photo-catalyst (Zn3V2O8/rGO). This work proposes a new photo-catalyst for H2 production application. We believe that the presence of synergistic interactions was responsible for the improved photo-catalytic properties of Zn3V2O8/rGO composite. The Zn3V2O8/rGO composite is an environmentally friendly and cost-effective photo-catalyst and can be used for photo-catalytic applications.

Aromatic amines are important chemical intermediates that hold an irreplaceable significance for synthesizing many chemical products. However, they may react with substances excreted from human bodies to generate blood poisoning, skin eczema, and dermatitis disease and even induce cancer-causing high risks to human health and the environment. Metal tungstates have been proven to be highly efficient materials for developing various toxic gases or chemical detection sensor systems. However, the major factors of the sensors, such as sensitivity, selectivity, stability, response, and recovery times, still need to be optimized for practical technological applications. In this work, Ni-doped ZnWO4 mixed metal tungstate nanocomposite material was synthesized by the hydrothermal method and explored as a sensor for the fluorometric determination of p-nitroaniline (p-NA). Transmission electron microscopy (TEM) was used for the elucidation of the optimized particle diameter. Scanning electron microscopy (SEM) was employed to observe the surface morphological changes in the material during the solid-state reactions. The vibration modes of as-prepared samples were analyzed using Fourier-transform infrared spectroscopy (FTIR). The chemical bonding and oxidation states of individual elements involved in material synthesis were observed using X-ray photoelectron spectroscopy (XPS). The PL activities of the metal tungstate nanoparticles were investigated for the sensing of p-nitroaniline (p-NA). The obtained results demonstrated that ZnNiWO4 was more effective in sensing p-NA than the other precursors were by using the quenching effect. The material showed remarkably high sensitivity towards p-NA in a concentration range of 25–1000 μM, and the limit of detection (LOD) value was found to be 1.93 × 10−8 M for ZnWO4, 2.17 × 10−8 M for NiWO4, and 2.98 × 10−8 M for ZnNiWO4, respectively.

In this study, a new bio-adsorbent (NASIF) was successfully prepared via chemical activation of Solanum incanum (SI) with hydrogen peroxide and sodium hydroxide reagents as an inexpensive and effective adsorbent for the removal of methylene blue (MB) from aqueous media. The morphology of the NASIF adsorbent surface and the nature of the potential MB interactions were examined by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) micrograph. FTIR results suggested that carboxyl, carbonyl, and hydroxyl groups were involved in MB adsorption on the NASIF surface. EDX analysis confirmed the successful increase of oxygen-containing functional groups during the chemical activation. The influence of important factors was studied using the batch method. The results revealed that the maximum removal efficiency was 98% at contact time: 120 min; pH: 6.5, adsorbent dose: 40 mg; and temperature-25 °C. Isothermal behavior was evaluated using three non-linear isotherm models, Langmuir, Freundlich, and D–R isotherm. MB adsorption onto NASIF adsorbent followed the Langmuir isotherm model with maximum monolayer capacity (mg/g) at 25 °C. Meanwhile, the PSO kinetics model was found to be better than PFO kinetic model for describing the adsorption process using kinetic models. Based on the D–R model, the free energy (E, kJ mol−1) values were in the range of 0.090–0.1812 kJ mol−1, which indicated that the MB adsorption onto NASIF may belong to physical adsorption. The adsorption mechanism of MB onto NASIF adsorbent mainly includes electrostatic attraction, π-π interaction, n-π interaction, and H-bonding. The thermodynamic parameters revealed that the adsorption process was a feasibility, spontaneous and exothermic process. Finally, the result of the present work could provide strong evidence of the potential of NASIF adsorbent for eliminating MB from aqueous media.

The monoclinic nanocrystalline Ni1−xMnxWO4 heterostructure has been successfully synthesized by the hydrothermal technique for achieving better sensitive and photocatalytic performances. Different characterization techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), ultraviolet-visible (UV–Vis), and photoluminescence (PL) spectroscopy have been employed to investigate their structural, microstructural, and optical properties. Mn-ion incorporation in the NiWO4 lattice reduces the particle size of the sample compared with the pure undoped NiWO4 sample, which has been confirmed from the transmission electron microscope image. The Tauc plot of the Ni1−xMnxWO4 sample exhibits a significant decrease in bandgap energy compared with the pure undoped NiWO4 sample due to the quantum confinement effect. Finally, the material was explored as a photocatalyst for the degradation of methyl orange (MO) dye from wastewater under visible light irradiation. Various reaction parameters such as pH, catalyst dose, reaction time, and kinetics of the photodegradation were studied using the batch method. The results showed that the Ni1−xMnxWO4 is highly efficient (94.51%) compared with undoped NiWO4 (65.45%). The rate of photodegradation by Ni1–xMnxWO4 (0.067) was found to be 1.06 times higher than the undoped NiWO4 (0.062).

In the present study, pristine ZnWO4, CoWO4, and mixed metal Zn0.5Co0.5WO4 were synthesized through the hydrothermal process using a Teflon-lined autoclave at 180 ℃. The synthesized nanomaterials were characterized by various spectroscopic techniques, such as TEM, FTIR, UV–vis, XRD, and SEM-EDX-mapping to confirm the formation of nanocomposite material. The synthesized materials were explored as photocatalysts for the degradation of xylenol orange (XO) under a visible light source and a comparative study was explored to check the efficiency of the bimetallic co-doped nanocomposite to the pristine metal tungstate NPs. XRD analysis proved that reinforcement of Co2+ in ZnWO4 lattice results in a reduction in interplanar distance from 0.203 nm to 0.185 nm, which is reflected in its crystallite size, which reduced from 32 nm to 24 nm. Contraction in crystallite size reflects on the optical properties as the energy bandgap of ZnWO4 reduced from 3.49 eV to 3.33 eV in Zn0.5Co0.5WO4, which is due to the formation of a Z-scheme for charge transfer and enhancement in photocatalytic efficiency. The experimental results suggested that ZnWO4, CoWO4, and Zn0.5Co0.5WO4 NPs achieved a photocatalytic efficiency of 97.89%, 98.10%, and 98.77% towards XO in 120 min of visible solar light irradiation. The kinetics of photodegradation was best explained by pseudo-first-order kinetics and the values of apparent rate const (kapp) also supported the enhanced photocatalytic efficiency of mixed metal Zn0.5Co0.5WO4 NPs towards XO degradation.