Synthesis Optimization of Activated Carbon Driven from Scrap Tire for Adsorbent Yield and Methylene Blue Removal under Response Surface Methodology

Abstract

This study aimed to investigate the synthesis optimization of activated carbon-driven scrap tires for adsorbent yield and methylene blue removal under response surface methodology. The scrap tire sample was activated by KOH using ethanol as a solvent. The optimized activated carbon was characterized using proximate analysis, scanning electron microscope (SEM), X-ray diffraction (XRD), and Brunauer Emmett Teller (BET) method. The activated carbon was demineralized using 5 M NaOH + 98% H2SO4 (1 : 1) as a solvent to enhance the surface area. Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich models were used to check the adsorption isotherm. The adsorption kinetics was checked using pseudo-first-order and pseudo-second-order models. Weber-Morris intraparticle diffusion model was used to study the diffusion mechanism. The optimum impregnation ratio, impregnation time, and carbonization temperature for synthesizing the activated carbon were 2 g/g, 12 hr, and 700°C, respectively. The moisture content, volatile matter, ash content, fixed carbon, and bulk density of the activated carbon were 6.13%, 9.42%, 5.34%, 79.11%, and 0.89 mg/L, respectively. The surface area of optimized activated carbon was enhanced by demineralization process and increased from 53 m2/g to 260.26 m2/g. Temkin adsorption isotherm with R2 values of 0.982 and pseudo-second-order adsorption kinetics with R2 values of 0.999 best fits the experimental data respectively. Intraparticle diffusion was not the only rate-controlling step for both optimized and demineralized (NaOH + H2SO4) activated carbon. It can be concluded that the optimized and demineralized activated carbon derived from scrap tires has a promising potential to be used as a low-cost adsorbent in developing countries including Ethiopia. However, further investigation needs to be conducted before scaling up at industrial level.