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For the first time, activated carbon from a durian shell (ACDS) activated by H2SO4 was successfully synthesized in the present study. The fabricated ACDS has a porous surface with a specific surface area of 348.0017 m2·g−1, average capillary volume of 0.153518 cm3·g−1, the average pore diameter of 4.3800 nm; ash level of 55.63%; humidity of 4.74%; density of 0.83 g·cm−3; an iodine index of 634 mg·g−1; and an isoelectric point of 6.03. Several factors affecting Methylene Blue (MB) adsorption capacity of ACDS activated carbon was investigated by the static adsorption method, revealing that the adsorption equilibrium was achieved after 90 min. The best adsorbent pH for MB is 7 and the mass/volume ratio is equal to 2.5 g·L−1. The MB adsorption process of ACDS activated carbon follows the Langmuir, Freundlich, Tempkin, and Elovich isotherm adsorption model, which has determined the maximum adsorption capacity for MB of ACDS as qmax = 57.47 mg·g−1. The MB adsorption process of ACDS follows the of pseudo-second-order adsorption kinetic equation. The Weber and Morris Internal Diffusion Model, the Hameed and Daud External Diffusion Model of liquids have been studied to see if the surface phase plays any role in the adsorption process. The results of thermodynamic calculation of the adsorption process show that the adsorption process is dominated by chemical adsorption and endothermic. The obtained results provide an insight for potential applications of ACDS in the treatment of water contaminated by dyes.

In this study, we report on the preparation of copper oxide/strontium titanate/multi-walled carbon nanotube (CuO/STO/MWCNTs) nanocomposites and their photocatalytic activity for degradation of dye under visible light. The crystalline structures of the nanocomposites were investigated by an X-ray diffraction (XRD) technique, which explored the successful fabrication of CuO/STO/MWCNTs nanocomposites, and the cubic STO phase was formed in all samples. For the morphological study, the transmission electron microscope (TEM) technique was used, which had proved the successful preparation of CuO and STO nanoparticles. The energy dispersive X-ray spectroscopy (EDX), dark field scanning transmission electron microscope (DF-STEM-EDX mapping), and X-ray photoelectron spectra (XPS) analysis were performed to evidence the elemental composition of CuO/STO/MWCNTs nanocomposites. The optical characteristics were explored via UV–Vis diffuse reflectance spectroscopy (DRS) and photoluminescence (PL) techniques. These studies clearly indicate the effect of the presence of CuO and MWCNTs on the visible absorption of the CuO/STO/MWCNTs nanocomposites. The photocatalytic activity of CuO/STO/MWCNTs nanocomposites was evaluated by the degradation of methylene blue (MB) dye under visible light irradiation, following first-order kinetics. Among the different x% CuO/STO/MWCNTs nanocomposites, the 5 wt.% CuO/STO/MWCNTs nanocomposites showed the highest photocatalytic efficiency for the degradation of MB dye. Moreover, the 5% CuO/STO/MWCNTs showed good stability and recyclability after three consecutive photocatalytic cycles. These results verified that the optimized nanocomposites can be used for photocatalytic applications, especially for dye degradation under visible light.

In this study, activated carbon derived from mangosteen peel (abbreviated as ACMP) was successfully fabricated. This as-prepared ACMP possessed graphite and had a porous structure with a specific surface area of 419.8554 m2/g. Investigations of the influencing factors on the ciprofloxacin (CIP) adsorption capability of the ACMP based on the static adsorption method showed that: adsorption equilibrium can be achieved in 60 min, the optimal pH for CIP adsorption was a pH of 6, and the optimal ratio between the material mass and solution volume was 3 g/L. The CIP adsorption process of the ACMP follows the Langmuir, Freundlich, Tempkin, Elovich, and Redlich–Peterson isotherm adsorption models. The maximum adsorption capacity calculated according to the Langmuir isothermal adsorption model for the CIP of the ACMP was (qmax = 29.76 mg/g). The CIP adsorption process of the ACMP followed the apparent quadratic kinetic equation, as well as spontaneous, endothermic, physical, and chemical adsorption. The adsorption rate was governed by membrane diffusion.

A CuO-loaded SrTiO3 catalyst showed highly photocatalytic activity for H2 evolution. This catalyst was prepared by an impregnation method and characterized by XRD, TEM, BET, XPS, Uv-vis DRS and PL techniques. Under optimum conditions, the best rate of H2 evolution of the CuO-loaded SrTiO3 catalyst is 5811 µmol h−1g−1, whereas it is a mere 34 µmol h−1g−1 for the pure SrTiO3. High efficiency, low cost and good stability are some of the merits that underline the promising potential of CuO-loaded SrTiO3 in the photocatalytic hydrogen.