Efficiency of a novel cysteine-polypyrrole@silver phosphate nanocomposite for hazardous Cr(VI) removal: Experimental study and statistical optimization modeling
DATE:
2024-11
UNIVERSAL IDENTIFIER: http://hdl.handle.net/11093/7874
EDITED VERSION: https://linkinghub.elsevier.com/retrieve/pii/S0167732224025789
DOCUMENT TYPE: article
ABSTRACT
A novel cysteine functionalized-Polypyrrole@silver phosphate (Cys-PPy@Ag3PO4) nanocomposite, synthesized through chemical polymerization was used for fully reducing Cr(VI) to Cr(III) and successfully capturing the Cr(III), representing a major leap in Cr(VI) remediation technology. Assorted analytical approaches, such as Fourier-transforms infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), X-ray photoelectron (XPS) spectroscopy, Brunauer-Emmett-Teller (BET), scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS), were implemented to explore the morphology and removal mechanism. The nanocomposite exhibited a mesoporous structure enriched with nitrogen/oxygen functional groups, which improved the diffusion, adsorption, and reduction of Cr(VI) ions. At pH 2, 96.50 % of Cr(VI) was removed using 0.5 g.L−1 of adsorbent in 60 min. Besides, the maximum uptake capability was 14.76 mg.g−1, and both Freundlich isotherm and PSO kinetic models perfectly aligned with the adsorption experimental findings for Cr(VI) species. Analysis of thermodynamic factors revealed that Cr(VI) adsorption was endothermic and spontaneous, enhancing the disorder of Cr(VI) species on the nanocomposite surface. XPS and FT-IR analysis proved that Cr(VI) ions were electrostatically adsorbed and subsequently converted to Cr(III), which were then immobilized through chelation with imine/sulfonate groups and electrostatic attraction with carboxylate groups. The nanocomposite showcased effortless regenerability through basification and outstanding reusability. Overall, Cys-PPy@Ag3PO4 proved highly effective in removing Cr(VI) from water