Enhanced benzene vapor adsorption through microwave-assisted fabrication of activated carbon from peanut shells using ZnCl2 as an activating agent.

Herein, microwave-assisted activated carbon (MW-AC) was fabricated from peanut shells using a ZnCl2 activator and utilized for the first time to eliminate benzene vapor as a volatile organic compound (VOC). During the MW-AC production process, which involved two steps-microwave treatment and muffle furnace heating-we investigated the effects of various factors and achieved the highest iodine number of 1250 mg/g. This was achieved under optimal operating conditions, which included a 100% impregnation ratio, CO2 as the gas in the microwave environment, a microwave power set at 500 W, a microwave duration of 10 min, an activation temperature of 500 °C and an activation time of 45 min. The structural and morphological properties of the optimized MW-AC were assessed through SEM, FTIR, and BET analysis. The dynamic adsorption process of benzene on the optimized MW-AC adsorbent, which has a significant BET surface area of 1204.90 m2/g, was designed using the Box-Behnken approach within the response surface methodology. Under optimal experimental conditions, including a contact duration of 80 min, an inlet concentration of 18 ppm, and a temperature of 26 °C, the maximum adsorption capacity reached was 568.34 mg/g. The experimental data are better described by the pseudo-second-order kinetic model, while it is concluded that the equilibrium data are better described by the Langmuir isotherm model. MW-AC exhibited a reuse efficiency of 86.54% for benzene vapor after five consecutive recycling processes. The motivation of the study highlights the high adsorption capacity and superior reuse efficiency of MW-AC adsorbent with high BET surface area against benzene pollutant. According to our results, the developed MW-AC presents itself as a promising adsorbent candidate for the treatment of VOCs in various industrial applications.

Novel adsorbent for malachite green from okra stalks waste: synthesis, kinetics and equilibrium studies.

In this study, malachite green (MG) removal was performed with activated carbon synthesized from okra stalks by microwave assisted chemical activation method. In the synthesis of activated carbon, the effects of gas in the microwave, activation, and impregnation rate were investigated. The synthesized activated carbon characterization was investigated using BET, FT-IR, and SEM analyses. The activated carbon surface area achieved was 759.453 m2 g-1. In addition, the surface area of activated carbon synthesized using the conventional method was17.766 m2 g-1. The effect of the initial solution concentration on MG adsorption was investigated. According to the kinetic and equilibrium data, it was found that the adsorption process best fitted the pseudo-second order kinetic model and the Langmuir isotherm. According to the equilibrium data, the maximum adsorption capacity (qmax) of the monolayer was 119.05 mg g-1. In addition, MG adsorption was investigated by the experimental design method. The adsorption capacity at the determined optimum conditions was 99.63 mg g-1. All results show that activated carbon synthesized from waste biomass by combining the conventional method with microwave-assisted impregnation is a cheap and environmentally friendly adsorbent.

The synthesis of activated carbon from waste biomass using the conventional activation method is quite common. Activated carbon synthesis studies have increased in recent years with microwave-assisted impregnation, which has been integrated into the conventional activation method. Using this new method, the synthesis of activated carbon from okra stalk waste was carried out for the first time in this study. In addition, with this novel adsorbent, malachite green was removed from the aqueous solutions for the first time.

Designing novel perlite-Fe3O4@SiO2@8-HQ-5-SA as a promising magnetic nanoadsorbent for competitive adsorption of multicomponent VOCs.

Volatile organic compounds (VOCs), which emerge as multicomponent pollutants through many industrial processes, pose a serious threat to human health and the eco-environment due to their volatility, toxicity and dispersion. Hence, the study of competitive adsorption of multicomponent VOCs is of practical and scientific importance. Herein, the perlite-supported Fe3O4@SiO2@8-hydroxyquinoline-5-sulfonic acid (perlite-Fe3O4@SiO2@8-HQ-5-SA) was designed as a novel magnetic nanoadsorbent by a simple strategy and employed for the competitive adsorption of multicomponent toluene, ethylbenzene and xylene in the vapor-phase targeted as VOCs. The successfully prepared perlite-Fe3O4@SiO2@8-HQ-5-SA was characterized by means of SEM, EDX, FT-IR, VSM and BET analyses. Adsorption capacities of 558 mg/g, 680 mg/g and 716 mg/g were achieved for single component toluene, ethylbenzene and xylene, respectively. It was concluded that the adsorption capacities for both binary and ternary components were significantly decreased compared to single component adsorption. The competitive adsorption capacity order of the binary and ternary component VOCs was xylene > ethylbenzene > toluene due to their competitive dominance. The rate-limiting kinetic analysis indicated that the adsorption rates were determined by both the film diffusion and intraparticle diffusion. The analysis of the error metrics demonstrated that the three-parameter isotherm models better described the adsorption data compared to the two-parameter models. In particular, the Toth model provided the closest fit to the experimental equilibrium data. The thermodynamic analysis indicated the spontaneous nature and probability (ΔG° <0), exothermic (ΔH° <0), physical (ΔH° <20 kJ/mol) and a declination in the degree of randomness (ΔS° <0) of the adsorption processes. The reuse efficiency of perlite-Fe3O4@SiO2@8-HQ-5-SA for toluene, ethylbenzene and xylene decreased to only by 88.91%, 88.07% and 87.16% after five recycles. The perlite-Fe3O4@SiO2@8-HQ-5-SA has a significant adsorptive potential compared to other adsorbents reported in the literature, thus it could be recommended as a promising nanoadsorbent for VOCs in industrial processes.

Superior incident photon-to-current conversion efficiency of Mo-doped activated carbon supported CdS-sensitized solar cells.

In this study, the performance of activated carbon (AC) produced from defatted black cumin (Nigella sativa L.) by chemical activation with zinc chloride (ZnCl2) activator in photovoltaic application is evaluated. It is of great importance to increase the photovoltaic efficiency of cadmium sulfide (CdS)-based solar cells, which are widely used in photovoltaic applications, with AC support. The main purpose of the study is to determine how the incident photon-to-current conversion efficiency (IPCE) of undoped and Mo-doped AC supported CdS semiconductor materials changes in the presence of AC support material and to interpret the observed effect in the light of literature. For these reasons, in the study, AC supported CdS (CdS/AC) (5%, 10%, and 15% by weight) and Mo-doped CdS/AC semiconductor materials with different molybdenum (Mo) concentrations (0.33%, 1%, 3%) are produced by chemical precipitation method. Produced CdS/AC and Mo-doped CdS/AC semiconductor materials are characterized by IPCE, scanning electron microscopy (SEM), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS) measurements. Based on the result values, the optimum CdS concentration with the highest IPCE (%) value is determined as 10% (for CdS/AC). As a result of the experimental measurements, the optimum Mo concentration with the maximum IPCE (%) value is found as 1% (for Mo-doped CdS/AC). In particular, it is clear that an appreciable increase (from 4.70 to 39.00%) in IPCE (%) of 1% Mo-doped 10% CdS/AC semiconductor material is achieved when compared to pure CdS. Thus, the ability to increase the photovoltaic efficiency of CdS-based solar cells, which are widely used in photovoltaic applications, with AC support has been clearly demonstrated. This study presents a new strategy to increase the solar cell efficiency of semiconductor-based solar cell structures using biowaste-based AC supported CdS semiconductor materials.

Green synthesis of copper oxide and manganese oxide nanoparticles from watermelon seed shell extract for enhanced photocatalytic reduction of methylene blue.

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.

Preparation and characterization of activated carbon from hydrochar by hydrothermal carbonization of chickpea stem: an application in methylene blue removal by RSM optimization.

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°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°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 (Qmax) 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.

Fabrication and characterization of 3,4-diaminobenzophenone-functionalized magnetic nanoadsorbent with enhanced VOC adsorption and desorption capacity.

The present study, for the first time, utilized 3,4-diaminobenzophenone (DABP)-functionalized Fe3O4/AC@SiO2 (Fe3O4/AC@SiO2@DABP) magnetic nanoparticles (MNPs) synthesized as a nanoadsorbent for enhancing adsorption and desorption capacity of gaseous benzene and toluene as volatile organic compounds (VOCs). The Fe3O4/AC@SiO2@DABP MNPs used in adsorption and desorption of benzene and toluene were synthesized by the co-precipitation and sol-gel methods. The synthesized MNPs were characterized by SEM, FTIR, TGA/DTA, and BET surface area analysis. Moreover, the optimization of the process parameters, namely contact time, initial VOC concentration, and temperature, was performed by applying response surface methodology (RSM). Adsorption results demonstrated that the Fe3O4/AC@SiO2@DABP MNPs had excellent adsorption capacity. The maximum adsorption capacities for benzene and toluene were found as 530.99 and 666.00 mg/g, respectively, under optimum process parameters (contact time 55.47 min, initial benzene concentration 17.57 ppm, and temperature 29.09 °C; and contact time 57.54 min, initial toluene concentration 17.83 ppm, and temperature 27.93 °C for benzene and toluene, respectively). In addition to the distinctive adsorptive behavior, the Fe3O4/AC@SiO2@DABP MNPs exhibited a high reproducibility adsorption and desorption capacity. After the fifth adsorption and desorption cycles, the Fe3O4/AC@SiO2@DABP MNPs retained 94.4% and 95.4% of its initial adsorption capacity for benzene and toluene, respectively. Kinetic and isotherm findings suggested that the adsorption mechanisms of benzene and toluene on the Fe3O4/AC@SiO2@DABP MNPs were physical processes. The results indicated that the successfully synthesized Fe3O4/AC@SiO2@DABP MNPs can be applied as an attractive, highly effective, reusable, and cost-effective adsorbent for the adsorption of VOC pollutants.Graphical abstract.

A comprehensive new study on the removal of Pb (II) from aqueous solution by sirnak coal-derived char.

In this study, char was prepared from the Sirnak coal derivative as a new adsorbent by the pyrolysis process and successfully applied for Pb (II) removal. Prepared char adsorbent was characterized by analysis techniques such as thermogravimetric (TG)/differential thermogravimetric (DTG), iodine number, scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and Brunauer-Emmett-Teller (BET) surface area. In the experimental design of the Pb (II) removal process, the relationship between operating factors (contact time, initial Pb (II) concentration and temperature) and process responses (adsorption capacity and removal efficiency) was modelled by applying response surface methodology (RSM). After that, the operating factors for the maximum adsorption capacity and removal efficiency of Pb (II) by char were optimized. In the removal of Pb (II), pseudo-first order and pseudo-second order kinetic models were used to determine the process mechanism. In addition, adsorption isotherm models such as Langmuir, Freundlich, and Dubinin-Radushkevich were applied to the equilibrium data to explain the adsorption mechanism between the adsorbent and adsorbate molecules. According to the results obtained, it was determined that kinetic and equilibrium isotherm data were better defined with pseudo-second order kinetic and Dubinin-Radushkevich isotherm models, respectively. The optimum values of the contact time, initial Pb (II) concentration, and temperature for maximum adsorption capacity (124.64 mg/g) and removal efficiency (92.35%) of Pb (II) were found as 150.00 min, 144.81 ppm, and 35.06°C, respectively. This study indicated the application potential of Sirnak coal-derived char as a promising cost-effective adsorbent for the removal of heavy metals.

High-performance gas-phase adsorption of benzene and toluene on activated carbon: response surface optimization, reusability, equilibrium, kinetic, and competitive adsorption studies.

In recent years, volatile organic compounds (VOCs) have become a group of major pollutants that endanger human health and the ecological environment. The main purpose of this study was to investigate the gas-phase adsorption processes of benzene and toluene, which are important VOCs, on the activated carbon (AC) produced from Elaeagnus angustifolia seeds by physical activation method. In this context, the central composite design (CCD) approach-based response surface methodology (RSM) was applied to examine and optimize the effects of process parameters on the adsorption of benzene and toluene by AC adsorbent. The characterization of the produced AC was performed by the Brunauer-Emmett-Teller surface area, scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray diffraction analysis. The optimum process parameters were achieved (adsorption time of 74.98 min, initial benzene concentration of 16.68 ppm, and temperature of 26.97 °C, and adsorption time of 73.26 min, initial toluene concentration of 18.46 ppm and temperature of 29.80 °C) for benzene and toluene, respectively. The maximum adsorption capacities of benzene and toluene on AC were determined to be 437.36 and 512.03 mg/g, respectively, under optimum parameters. The adsorption process kinetics and equilibrium isotherms were also evaluated. Besides, AC reusability studies were performed five times for the gas-phase adsorption and desorption of benzene and toluene. After five cycles, it was observed that the benzene and toluene adsorption capacity of the AC decreased slightly by 8.10% and 7.42%, respectively. The results revealed that the produced AC could be utilized successfully for the removal of benzene and toluene in the gas-phase adsorption systems because of its high surface area, high adsorption capacity, and high reusability performance. Furthermore, the adsorption processes of benzene and toluene were investigated, both sole components and in a binary mixture. It was concluded that the adsorption behaviors of benzene and toluene against AC were quite different when they were in the competition (in a binary mixture) and without competition (sole components). Graphical abstract.