Herein, mesoporous activated carbon (AC) was prepared through potassium hydroxide (KOH) activation of hydrochar derived from the hydrothermal carbonization (HTC) of chickpea stem (CS), and successfully applied to remove methylene blue (MB) dye from aqueous solutions in a batch system. The HTC-CSAC was prepared depending on different impregnation ratios (hydrochar:KOH, 50–150%), impregnation times (12–48 h), activation temperatures (400–600 $°\mathrm{C}$) and activation times (30–60 min). To define HTC-CSAC, various analytical techniques such as iodine adsorption number (IAN), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and Brunauer–Emmett–Teller (BET) were used. In the removal process of MB by the best HTC-CSAC with a high IAN of 887 mg g⁻¹ obtained under conditions including impregnation ratio of 70%, activation time of 45 min, activation temperature of 600 $°\mathrm{C}$ and impregnation time of 24 h, the effects of adsorption parameters such as pH factor (2–10), adsorbent dosage (50–100 mg), initial MB concentration (40–80 mg/L) and contact time (90–180 min) were studied. Besides, a detailed evaluation of the adsorption mechanism for the removal of MB by HTC-CSAC was performed. The Langmuir model indicated the best isotherm data correlation, with a maximum monolayer adsorption capacity (Q_max) of 96.15 mg g⁻¹. The adsorption isotherm findings demonstrated that the MB removal process is feasible, and that this process takes place through the physical interaction mechanism. Additionally, the HTC-CSAC adsorbent exhibited a high regeneration and reuse performance in MB removal. After five consecutive adsorption-desorption cycles, HTC-CSAC maintained the reuse efficiency of 77.86%. As a result, the prepared HTC-CSAC with a high BET surface area of 455 m² g⁻¹ and an average pore diameter of 105 Å could be recommended as a promising and reusable adsorbent in the treatment of synthetic dyes in wastewaters. Graphical Abstract

In the current study, copper oxide (CuO) and manganese oxide (MnO) nanoparticles (NPs) were synthesized through a simple, cost-efficient, and green method using watermelon seed shell extract as a stabilizing and reducing agent. The synthesized CuO and MnO NPs were characterized by using scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and Ultraviolet spectroscopy (UV). The particle sizes of CuO and MnO NPs were determined to be in the range of 15–97 and 6–51 nm, respectively, by TEM and XRD analysis. The photocatalytic performance of the CuO and MnO NPs used as catalysts were investigated for the photocatalytic reduction of methylene blue in an aqueous solution. In the photocatalytic reduction of methylene blue, sodium borohydride (NaBH₄) was used as the reducing agent. The CuO and MnO NPs were capable to remove 96.58% (in 70 min) and 96.60% (in 140 min) of methylene blue from aqueous media, respectively. Besides, the kinetics of the photocatalytic reaction was investigated by a pseudo-first order model, and the reaction rate coefficient for methylene blue with CuO and MnO NPs were calculated as 0.0426 and 0.0235 min⁻¹, respectively. The results demonstrated that the synthesized CuO and MnO NPs through the green method were promising catalysts to improve the photocatalytic reduction performance of methylene blue. NOVELTY STATEMENT The copper oxide (CuO) and manganese oxide (MnO) nanoparticles (NPs) were synthesized from watermelon seed extract by the green synthesis method. The watermelon seed shell, which is left as waste to the environment, has been transformed into a product with high added value. The particle sizes of CuO and MnO NPs were determined to be in the range of 15–97 and 6–51 nm, respectively. The photocatalytic performance of the CuO and MnO NPs used as catalysts were investigated for the photocatalytic reduction of methylene blue in an aqueous solution. In the photocatalytic reduction of methylene blue, sodium borohydride (NaBH₄) was used as the reducing agent. The CuO and MnO NPs were capable to remove 96.58% (in 70 min) and 96.60% (in 140 min) of methylene blue, respectively. It was determined that UV light was effective in the photocatalytic reduction of methylene blue with NaBH₄. The reaction rate coefficient for the photocatalytic reduction of methylene blue with CuO and MnO NPs was calculated as 0.0426 and 0.0235 min⁻¹, respectively.

In this study, activated carbon was obtained from Elaeagnus angustifolia seeds and its usability in the adsorption of methylene blue (MB) and malachite green (MG) from aqueous solution was investigated. Activated carbon was synthesized by chemical activation method using H₃PO₄ as an activator. In the synthesis of the activated carbon, the effects of various parameters such as the rate of impregnation, duration of activation, temperature of activation and duration of activation were investigated. The characterization of the synthesized activated carbons was carried out by FTIR, SEM and BET analyses and the surface area of the produced activated carbon was determined to be 1,194 m² g⁻¹. The effects of solution initial pH, solution initial concentration and amount of activated carbon on MB and MG adsorption were investigated. The adsorption capacity was found to be higher when the pH of the solution was 8 for MB and 4 for MG. The adsorption kinetics of MB and MG were found to fit the Elovich kinetic model and pseudo-first-order kinetic model, respectively. Adsorption equilibrium data were found to be compatible with Langmuir isotherm for both dyes. According to the Langmuir isotherm, q _max adsorption capacity was found to be 72 mg/g and 115 mg/g for MB and MG, respectively. Novelty Activated carbon was obtained from Elaeagnus angustifolia seeds and its usability in the adsorption of methylene blue (MB) and malachite green (MG) from aqueous solution was investigated. A high surface area activated carbon was synthesized. The surface area of the produced activated carbon was determined to be 1,194 m² g⁻¹. According to the Langmuir isotherm, q _max adsorption capacity was found to be 72 mg/g and 115 mg/g for MB and MG, respectively. It has been determined that the adsorption capacity of synthesized activated carbon is high.

The efficient adsorption application and electric double-layer capacitor material with low-cost biomass-based activated carbon materials have been quite common recently. In this study, chestnut shell-based activated carbons were produced by chemical activation. ZnCl₂, H₃PO₄, and KOH agents were used for chemical activation. The obtained activated carbon, iodine adsorption from aqueous solutions, and its use as an electro capacitor were investigated. The scanning electron microscope, nitrogen adsorption/desorption, and Fourier transform infrared spectroscopy were used for characterization. The values of surface area and iodine adsorption capacity of the chestnut shell-based activated carbon are 1544 m² g⁻¹ and 1525 mg g⁻¹. As a result, a specific capacitance of 97 Fg⁻¹ with chestnut shell-based activated carbon was obtained in a 1 M KCl electrolyte for the electrochemical double-layer capacitor. This study shows that activated carbon based on the chestnut shell can be used both as an electrochemical energy storage material and as an adsorbent in iodine adsorption.