Rapid growth in various industrial fields has introduced a series of new environmental risks. The textile industry is one of the major industries that is influenced by rapid advancements in technological sectors. The development in textile dying technologies has presented new types of dyes that are toxic to the ecosystem. Azo dyes are the main artificial dyes used in textiles, food, and other applications. Typically, these dyes are introduced into the environment as wastewater discharged from factories. The discharged influence penetrates the ecosystem and causes deadly diseases to human and animals. Several studies present activated carbon as a proper solution to eliminating the presence of azo dyes in the environment. However, various types of azo dye have different properties and chemical structures. Thus, there is a crucial need for more studies on the application of activated carbons to eliminate the presence of azo dyes in the environment. This paper discusses the toxic effects of azo dyes on the environment and human health. Moreover, this work presents a general review of the preparation of activated carbon and the parameters that influence the adsorption performance.

This research deals with the effect of the temperature on the physical, thermal, electrochemical, and adsorption properties of the carbon micro-spheres using hydrothermal carbonization (HTC). Until recently, limited research has been conducted regarding the effects of delignification during the HTC process of biomass residues especially Dimocarpus longan. In this regard, lignin was first extracted from the lingo-cellulosic waste of Longan fruit peel (Dimocarpus longan). The holocellulose (HC) separated from lignin and raw biomass substrates (Longan fruit exocarp/peel powder, LFP) were carbonized at different temperatures using water as the green catalyst. Hydrothermal carbonization (HTC) was performed for both of the samples (LFP and HC) at 200 °C, 250 °C, and 300 °C for 24 h each. The surface morphological structures, the porosity, and the Brunauer-Emmett-Teller (BET) surface area of the prepared micro-spherical carbon were determined. The BET surface areas obtained for HC-based carbon samples were lower than that of the raw LFP based carbon samples. The carbon obtained was characterized using ultimate and proximate analyses. The surface morphological features and phase transformation of the synthesized micro-spherical carbon was characterized by a field-emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD) analysis. The results demonstrated that the extraction of lignin could significantly alter the end properties of the synthesized carbon sample. The carbon spheres derived from LFP showed a higher carbon content than the HC-based carbon. The absence of lignin in the holo-cellulose (HC) made it easy to disintegrate in comparison to the raw, LFP-based carbon samples during the HTC process. The carbonaceous samples (LFP-300 and HC-300) prepared at 300 °C were selected and their adsorption performance for Pb (II) cations was observed using Langmuir, Freundlich, and Temkin linear isotherm models. At 30 °C, the equilibrium data followed the Langmuir isotherm model more than the Freundlich and Temkin model for both the LFP-300 sample and the HC-300 sample. The potential of the synthesized carbon microspheres were further analyzed by thermodynamic characterizations of the adsorption equilibrium system.

Herein, we report the effect of synthesis temperature on the morphologies, optical and electronic properties of magnesium oxide (MgO) nanostructures. The MgO nanostructures were synthesized at different temperatures, i.e., 100 °C, 300 °C, and 600 °C by simple chemical reaction process and their morphology, particle size, optical, and electrical properties were examined by different techniques such as scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and UV-Vis. spectroscopy. The morphological investigations revealed that various morphologies of MgO nanostructures, i.e., nanoparticles, nanosheet networks, and nanoneedles were synthesized at 100 °C, 300 °C, and 600 °C. The XRD results confirmed that with increasing the synthesis temperature, the crystallinity of the synthesized nanostructures increases. Further, the dielectric properties and AC conductivity at various frequencies for MgO nanostructures were studied which revealed that the dielectric losses decrease with increase in frequency and temperature. In addition, the observed band gap decreases from 4.89 eV to 4.438 eV (100 °C to 600 °C) representing its increase in the conductivity.

Solid waste management needs re-evaluating in developing countries like Pakistan, which currently employs landfilling as a first option. Over time, increasing population will result in decreasing space for landfill sites, ultimately increasing the cost of landfilling, while increasing accumulated waste will cause pollution. Locating and preparing a sanitary landfill includes the securing of large sectors and also everyday activity with the end goal to limit potential negative impacts. Energy production from municipal solid waste (MSW) is a perceptive idea for large cities, such as Karachi, as waste, which is an undesirable output that adds to land and air pollution, is transformed into a vital source of energy. The current study strives to provide a destination to solid waste by evaluating the energy potential that waste provides for power generation by the process of incineration. A sustainable energy generation plant based on the Rankine cycle is proposed. This study evaluates the various landfill sites in the case study area to determine their sustainability for a waste to energy (WtE) plant. The implementation of the proposed plant will not only provide an ultimate destination to waste but also generate 121.9 MW electricity at 25% plant efficiency. Thus, the generated electricity can be used to run a WtE plant and meet the energy requirements of the residents.

In this study, lead sulfide (PbS) nanoparticles were synthesized by the chemical precipitation method using Aloe Vera extract with PbCl₂ and Thiourea (H₂N-CS-NH₂). The synthesized nanoparticles have been investigated using x-ray diffraction (XRD), UV-Vis, energy-dispersive x-ray spectroscopy (EDX), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). XRD and TEM results confirm that the films are in the cubic phase. The crystallite size, lattice constant, micro-strain, dislocation density, optical bandgap, etc. have been determined using XRD and UV-Vis for investigating the quality of prepared nanoparticles. The possible application of these synthesized nanoparticles in the solar cells was investigated by fabricating the thin films on an FTO-coated and bare glass substrate. The properties of nanoparticles were found to be nearly retained in the film state as well. The experimentally found properties of thin films have been implemented for perovskite solar cell simulation and current-voltage and capacitance-voltage characteristics have been investigated. The simulation results showed that PbS nanoparticles could be a potential hole transport layer for high-efficiency perovskite solar cell applications.