A detailed practical and theoretical study of the adsorptive potential of synthesised ceria impregnated activated graphite for aqueous Se(IV) and Te(IV) removal: Process optimisation, characterisation and mechanistic approach

Abstract

A cost-effective, simple, and earth friendly nanocomposite adsorbent was synthesized by in - situ penetration of ceria nanocrystals on graphite to remove aqueous selenium (IV) and tellurium (IV). Batch experiments optimize parameters such as pH, temperature, sorbent dosage and equilibration time of 30 minutes. The adsorbent exhibited the maximum adsorption capacities of 144.5 mg/g for Te(IV) and 29.3 mg/g for Se(IV). BET analysis revealed a specific surface area of 16.44 m²/g, an average pore diameter of 4.24 nm, and a high pore volume of 0.0519 cm³/g. The adsorbent was characterized before and after adsorption by SEM-EDX, XRD and FTIR. The sorption data could be well interpreted by the Langmuir model for both Se and Te and by the DR isotherm for Te(IV) at ambient temperature. Kinetic empirical data correlated positively with pseudosecond order for both Se and Te and the Elovich model for Te at room temperature. Kinetics and equilibrium isotherms suggested that the adsorption occurred through surface adsorption using electrostatic bonding along with physisorption involving steady diffusion and accommodation of analyte ions into mesopores and defects of the adsorbent. Chemisorption by electron transfer of the oxyanions of Se/Te with Ce³⁺/Ce⁴⁺ of the cerium impregnated graphite (CIAG) and ion exchange with functional groups on the activated graphite edges were other probable mechanisms. The adsorbent demonstrated the ability to be regenerated and reused over multiple cycles, with minimal interference from coexisting ions emphasizing its selectivity. All measurements were conducted in triplicate with the relative standard deviation (RSD) below 5 %. The optimised method was successfully applied in natural water samples from various sources, demonstrating strong potential for scaling up to field applications.