Microplastic (MP) is an emerging contaminant of concern due to its ubiquitous quantity in the environment, small size, and potential toxicity due to strong affinity towards other contaminants. In this work, MP particles (5-300 μm) were extracted from a commercial facial cleanser and determined to be irregular polyethylene (PE) microbeads based on characterization with field emission scanning electron microscopy (FESEM) and Raman spectroscopy. The potential of extracted MP acting as toxic pollutants' vector was analyzed via adsorption of methylene blue and methyl orange dye where significant dye uptake was observed. Synthetic wastewater containing the extracted MP was subjected to a continuous-flow column study using palm kernel shell and coconut shell biochar as the filter/adsorbent media. The prepared biochar was characterized via proximate and ultimate analysis, FESEM, contact angle measurement, atomic force microscopy (AFM), and Fourier transform infrared (FTIR) spectroscopy to investigate the role of the biochar properties in MP removal. MP removal performance was determined by measuring the turbidity and weighing the dry mass of particles remaining in the effluent following treatment. Promising results were obtained from the study with highest removal of MP (96.65%) attained through palm kernel shell biochar with particle size of 0.6-1.18 mm and continuous-flow column size of 20 mm.
Significant progress has been made over the years to improve the stability and efficiency of rapidly evolving tin-based perovskite solar cells (PSCs). One powerful approach to enhance the performance of these PSCs is through compositional engineering techniques, specifically by incorporating a mixed cation system at the A-site and B-site structure of the tin perovskite. These approaches will pave the way for unlocking the full potential of tin-based PSCs. Therefore, in this study, a theoretical investigation of mixed A-cations (FA, MA, EA, Cs) with a tin-germanium-based PSC was presented. The crystal structure distortion and optoelectronic properties were estimated. SCAPS 1-D simulations were employed to predict the photovoltaic performance of the optimized tin-germanium material using different electron transport layers (ETLs), hole transport layers (HTLs), active layer thicknesses, and cell temperatures. Our findings reveal that EA0.5Cs0.5Sn0.5Ge0.5I3 has a nearly cubic structure (t = 0.99) and a theoretical bandgap within the maximum Shockley-Queisser limit (1.34 eV). The overall cell performance is also improved by optimizing the perovskite layer thickness to 1200 nm, and it exhibits remarkable stability as the temperature increases. The short-circuit current density (Jsc) remains consistent around 33.7 mA/cm2, and the open-circuit voltage (Voc) is well-maintained above 1 V by utilizing FTO as the conductive layer, ZnO as the ETL, Cu2O as the HTL, and Au as the metal back contact. This configuration also achieves a high fill factor ranging from 87 % to 88 %, with the highest power conversion efficiency (PCE) of 31.49 % at 293 K. This research contributes to the advancement of tin-germanium perovskite materials for a wide range of optoelectronic applications.
Sulphur dioxide, a toxic gas pollutant, is mainly generated by the combustion of fossil fuels and the smelting of sulphur-bearing mineral ores. Removal of SO2 gas or desulphurisation can be accomplished in industries using a variety of processes; the most efficient is wet flue gas desulphurisation (FGD). However, wet FGD has challenges, such as the requirement for wastewater treatment, excessive water usage, and the necessity for chloride protective coating. Despite having a lesser adsorption capacity than wet FGD, dry FGD can efficiently remove SO2 from the effluent gas stream and avoid the issues associated with wet FGD, provided that the sorbents are modified and regenerable. An alternative dry desulphurisation strategy by using fibrous mesoporous silica (KCC-1) modified with deep eutectic solvents (DES), choline chloride-glycerol (DES1) and choline chloride-ethylene glycol (DES2) is studied in this paper. KCC-1 modified with DES1 is found to increase SO2 adsorption capacity to 4.83 mg g-1, which is 1.73 times greater than unmodified KCC-1 and twice higher than KCC-1 modified with DES2 attributed to the sorbent's high porosity. Increasing reaction temperature and SO2 concentration reduce the adsorption capacity to 1.73 mg g-1 and 2.73 mg g-1, respectively. The Avrami kinetic model and the Toth isotherm model best reflect SO2 adsorption on the modified KCC-1, indicating that SO2 molecules are adsorbed exothermically in multilayer adsorption on a heterogeneous surface through a combination of physical and chemical processes. The higher SO2 adsorption capacity of the modified KCC-1 suggests that choline chloride-glycerol can provide additional sites for SO2 adsorption in dry FGD technology.