Currently, conversion of coal into alternative fuel and non-fuel valuable products is in demand and growing interest. In the present study, humic acid was extracted from two different ranks of coal, i.e., low rank and high rank (lignite and bituminous), through chemical pretreatment by nitric acid. Samples of lignite and bituminous coal were subjected to nitric acid oxidation followed by extraction using KOH and NaOH gravimetric techniques. The chemical pretreatment of both types of coal led to enhanced yields of humic acid from 21.15% to 57.8% for lignite low-rank coal and 11.6% to 49.6% bituminous high rank coal. The derived humic acid from native coal and nitric acid treated coal was analyzed using elemental analysis, E4/E6 ratio of absorbance at 465 nm and 665 nm using UV-Visible spectrophotometry and Fourier transformed infrared spectroscopy FTIR. The chemical characteristics of coal treated with nitric acid have shown increased molecular weight and improved aromaticity with more oxygen and nitrogen and lower C, H, and sulphur content. The E4/E6 ratio of nitric acid-treated low and high ranks of coal was high. The FTIR spectroscopic data of nitric acid-treated lignite coal indicates an intensive peak of carboxyl group at 2981.84 cm⁻¹, while bituminous coal was shown in cooperation with the N-H group at 2923.04 cm⁻¹. SEM was performed to detect the morphological changes that happen after producing humic acid from HNO₃ treatment and native coal. The humic acid produced from HNO₃ treated coal had shown clear morphological changes and some deformations on the surface. SEM-EDS detected the major elements, such as nitrogen, in treated humic acid that were absent in raw coal humic acid. Hence, the produced humic acid through HNO₃ oxidation showed a more significant number of humic materials with improved efficiency as compared to native coal. This obtained humic acid can be made bioactive for agriculture purposes, i.e., for soil enrichment and improvement in growth conditions of plants and development of green energy solutions.

Water contaminated with heavy metals constitutes an important threat. This threat is a real problem with a negative impact in some developing countries where untreated industrial effluents are used for irrigation. The present study examines heavy metals in wastewater-irrigated vegetables (apple gourd, spinach, cauliflower, sponge gourd, and coriander) water, and soil from Chenab Nagar, Chiniot, Pakistan. In particular, the metals quantified were cadmium (Cd), chromium (Cr), cobalt (Co), nickel (Ni), lead (Pb), and manganese (Mn). Among them, Cr and Co in crops irrigated -wastewater exceeded the levels recommended by the World Health Organization (WHO). In contrast, Ni, Cu, Pb, and Mn concentrations were in line with WHO standards. Compared with the limits established by the Food and Agriculture Organization of the United Nations (FAO), all the study vegetables presented higher (thus unsafe) concentrations of Cd (0.38 to 1.205 mg/Kg). There were also unsafe concentrations of Cr in coriander, sponge gourd, and cauliflower. Pb was found at an unsafe concentration (0.59 mg/Kg) in cauliflower. Conversely, Ni and Mn concentrations were below the maximum permissible limits by WHO, and FAO in all of the analyzed samples. The contamination load index (CLI) in soil, bioconcentration factor (BCF) in plants, daily intake of metals (DIM), and health risk index (HRI) have also been evaluated to estimate the potential risk to human health in that area. We have found an important risk of transitions of Pb, Cd, Cr, and Co from water/soil to the edible part of the plant. The highest HRI value associated with Cd (6.10–13.85) followed by Cr (1.25–7.67) for all vegetable samples presented them as high health risk metal contaminants. If the issue is not addressed, consumption of wastewater-irrigated vegetables will continue posing a health risk.

Iron–copper bimetallic nanoparticles (Fe-Cu BNPs) were prepared via a green synthesis route. Ixora finlaysoniana has been used in this study as a capping and stabilizing agent in the modification of Fe-Cu BNPs. As-synthesized BNPs were characterized using different techniques including UV/Vis spectrophotometry, FTIR, XRD and SEM. A particle size analyzer and SEM studies indicated the particle size to be in the range of 50–200 nm. In addition, degradation of MB dye in an aqueous system and radical-scavenging potential in a DPPH assay were also examined using BNPs. Methylene blue dye degradation in 17 min was monitored with UV/Vis spectrophotometry, which exhibited the efficiency of Fe-Cu BNPs. Bimetallic nanoparticles were also found to be efficient in neutralizing DPPH free radicals. Furthermore, kinetic studies of both dye degradation and radical scavenging potential are reported in this article. Subsequently, Fe-Cu BNPs synthesized via a green and sustainable method can be employed for dye degradation and free radical-scavenging activities.

Heavy metals are the harmful elements, regarded as carcinogens. Nevertheless, owing to their physical and chemical properties, they are still used in the production of several commercial products. Utilization of such products increases the chance for the exposure of heavy metals, some of them are categorized as probable human carcinogens (Group 1) by the International Agency for Research on Cancer. Exposure of heavy metals to school children at early age can result severe life time health issues and high chance of emerging cancer. Thus, we have performed study relating to the presence of heavy metals in acrylic color paints commonly used by the school children. Acrylic paints of different colors were assayed for seven potential heavy metals manganese (Mn), cobalt (Co), nickel (Ni), zinc (Zn), arsenic (As), cadmium (Cd) and lead (Pb) using microwave digestion and iCAPQ inductively coupled plasma mass spectrometry (ICP-MS) system. The optimized method including paints digestion reagents nitric acid (HNO₃, 65%, 5 mL) and hydrofluoric acid (HF, 40%, 2 mL) have offered excellent method performance with recovery values ranged between 99.33% and 105.67%. The elements were identified in all of the analyzed samples with concentrations ranged from 0.05 to 372.59 µg/g. Cd constitutes the lower percentage (0.05%), whereas Zn constitutes high ratio contribution which was tremendously high (68.33%). Besides, the paints contamination was also color specific, with considerably total heavy metal concentrations found in brunt umber (526.57 µg/g) while scarlet color (12.62 µg/g) contained lower amounts. The outcomes of our investigation highlight the necessity for guidelines addressing the heavy metals in acrylic color paints intended for the school children usage.

This work intended to enhance the unique and outstanding properties of lanthanum by synthesizing its nanocomposite. A lanthanum-based nanocomposite was prepared by a simple and cost-effective “co-precipitation” method. Lanthanum nitrate (La (NO₃)₃) and zinc nitrate (Zn (NO₃)₂) were used as precursors. The lanthanum/zinc oxide nano composite formed was then calcined at 450 °C for 4 h in order to obtain a fine powder with size in the nano range of 1–100 nm. Characterization of the prepared catalyst was done by ultraviolet/visible spectroscopy, Fourier transform infrared spectroscopy, and photoluminescence. Crystallinity and morphology were found by X-ray diffraction and scanning electron microscopy. The synthesized nanocomposite material was also tested for heterogeneous catalytic applications of 4-nitrophenol (4-NP) reduction into 4-aminophenol (4-AP). It was found to be successful in complete reduction of 4-NP with enhanced catalytic performance.

Nanostructured Bismuth-based materials are promising electrodes for highly efficient electrochemical reduction processes such as hydrogen evolution reaction (HER). In this work, a novel sort of nanocomposite made up of partially reduced Bi₂O₃ into metallic Bi anchored on a 3D network of Ni-foam as a high-performance catalyst for electrochemical hydrogen reduction. The application of the hybrid material for HER is shown. The high catalytic activity of the fabricated electrocatalyst arises from the co-operative effect of Bi/Bi₂O₃ and Ni-foam which provides a highly effective surface area combined with the highly porous structure of Ni-foam for efficient charge and mass transport. The advantages of the electrode for the electrochemical reduction processes such as high current density, low overpotential, and high stability of the electrode are revealed. An overall comparison of our as-prepared electrocatalyst with recently reported works on related work is done.