Abstract
Wastewater treatment requires a lot of granular activated carbon to absorb the dissolved organic components. This article describes a low-cost process for making highly active adsorption activated carbons from biomass, which could be used for wastewater treatment. A one-step carbonization and chemical activation with phosphoric acid at 500 °C produced low-cost acacia-derived porous activated carbons. The activated carbons' moisture, ash, volatile matter, and fixed carbon content were determined using proximate analysis. The activated carbon's adsorption qualities were also determined by studying its bulk density, surface morphology, power of hydrogen, iodine number, and methylene blue number index. To test the produced activated carbons for water treatment, batch adsorption dynamics were performed at room temperature for the removal of methylene blue from aqueous solution. Compared to activation using H2SO4, H3PO4 proves superior in generating well-developed pores, leading to a mesoporosity and microporosity structure with a larger surface area and high adsorption capacity. Brunauer–Emmett–Teller determined the sample's specific surface area, which was found to be 387 m2/g. The iodine number for 50, 100, and 200 μm activated carbon particles size was 620, 592, and 632 mg/g, respectively. The adsorption of MB on AC material better fits with Langmuir's adsorption isotherm; hence, particles are adsorbed on well-pronounced heterogeneous surfaces. The sips model is found to best represent the equilibrium data with R2 values of 0.994, suggesting the heterogeneous surface adsorption of MB on AC. Therefore, the adsorption of AC by MB involves physical and chemical processes. The produced AC hence appears to remove dissolved organic contaminants from raw water.
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