4.7 Article

Removing methylene blue from water: A study of sorption effectiveness onto nanoparticles-doped activated carbon

Journal

CHEMOSPHERE
Volume 313, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2022.137533

Keywords

CSAC@AgNPs@TiO(2)NPs; Methylene blue; Adsorption; Surface modification; Mechanism; Comparative study

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In this study, a novel nanocomposite (CSAC@AgNPs@TiO(2)NPs) was synthesized by depositing silver (Ag) and titanium dioxide (TiO2) nanoparticles on coconut shell-derived activated carbon (CSAC) for the adsorption of Methylene Blue (MB) dye. The nanocomposite was characterized using various techniques and showed a high surface area of 301 m²/g. Adsorption experiments indicated that the Sips isotherm and pseudo-second-order models provided the best fits for the adsorption data. The CSAC@AgNPs@TiO(2)NPs exhibited excellent adsorption capacity and can be regenerated and reused multiple times.
In this present study, silver (Ag) and titanium dioxide (TiO2) nanoparticles were successfully deposited on co-conut shell-derived activated carbon (CSAC), to synthesize a novel nanocomposite (CSAC@AgNPs@TiO(2)NPs) for the adsorption of Methylene Blue (MB) dye from aqueous solution. The fabricated CSAC@AgNPs@TiO(2)NPs nanocomposite was analyzed by Scanning Electron Microscope (SEM), X-ray Diffraction (XRD), Fourier-Transform Infrared Spectroscopy (FTIR), Transmission Electron Microscope (TEM) equipped with Energy Dispersive X-ray spectroscopy (EDS) detector, X-ray Photoelectron Spectroscope (XPS), and Bru-nauer-Emmett-Teller (BET). The successful deposition of AgNPs and TiO(2)NPs on CSAC surface was revealed by the TEM/EDX, SEM, and XPS analysis. The mesopore structure of CSAC@AgNPs@TiO(2)NPs has a BET surface area of 301 m(2)/g. The batch adsorption studies were conducted and the influence of different parameters, i.e., adsorbent dose, adsorption time, initial dye concentration, pH and temperature were investigated. The nonlinear isotherm and kinetic modelling demonstrated that adsorption data were best fitted by Sips isotherm and pseudo-second-order models, respectively. The maximum adsorption capacity of MB onto CSAC@AgNPs@TiO(2)NPs by the Sips model was 184 mg/g. Thermodynamic results revealed that the adsorption was endothermic, spontaneous and physical in nature. CSAC@AgNPs@TiO(2)NPs revealed that MB absorption by CSAC@AgNP-s@TiO(2)NPs was spontaneous and endothermic. The uptake capacity of MB was influenced significantly by the presence of competing ions including, NO3-, HCO3, Ca2+, and Na+. Repeated tests indicated that the CSA-C@AgNPs@TiO(2)NPs can be regenerated and reused six times before being discarded. The primary separation mechanism between MB dye and CSAC@AgNPs@TiO(2)NPs was the electrostatic interaction. Thus, CSA-C@AgNPs@TiO(2)NPs was an outstanding material, which displayed good applicability in real water with >= 97% removal of MB dye.

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