The progress of industrial and agricultural pursuits, along with the release of inadequately treated effluents especially phenolic pollutant, has amplified the pollution load on environment. These organic compounds pose considerable challenges in both drinking water and wastewater systems, given their toxicity, demanding high oxygen and limited biodegradability. Thus, developing an eco-friendly, low-cost and highly efficient adsorbent to treat the organic pollutants has become an important task. The present investigation highlights development of a novel adsorbent (CFPAC) by activation of Cassia fistula pod shell for the purpose of removing phenol and 2,4-dichlorophnenol (2,4-DCP). The significant operational factors (dosage, pH, concentration, temperature, speed) were also investigated. The factors such as pH = 2 and T = 20°C were found to be significant at 1.6 g/L and 0.6 g/L dosage for phenol and 2,4-DCP respectively. Batch experiments were further conducted to study isotherms, kinetic and thermodynamics studies for the removal of phenol and 2,4-DCP. The activated carbon was characterised as mesoporous (specific surface area 1146 m/g, pore volume = 0.8628 cc/g), amorphous and pH = 6.4. At optimum conditions, the maximum sorption capacity for phenol and 2,4-DCP were 183.79 mg/g and 374.4 mg/g respectively. The adsorption isotherm was better conformed to Redlich Peterson isotherm (phenol) and Langmuir isotherm (2,4-DCP). The kinetic study obeyed pseudo-second-order type behaviour for both the pollutants with R > 0.999. The thermodynamic studies and the value of isosteric heat of adsorption for both the pollutants suggested that the adsorption reaction was dominated by physical adsorption (ΔH < 80 kJ/mol). Further, the whole process was feasible, exothermic and spontaneous in nature. The overall studies suggested that the activated carbon synthesised from Cassia fistula pods can be a promising adsorbent for phenolic compounds.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11685270PMC
http://dx.doi.org/10.1007/s11356-024-32971-1DOI Listing

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