Adsorption-desorption mechanism of phosphate by immobilized nano-sized magnetite layer: interface and bulk interactions

J Colloid Interface Sci. 2011 Nov 15;363(2):608-14. doi: 10.1016/j.jcis.2011.07.062. Epub 2011 Jul 27.

Abstract

Phosphate adsorption mechanism by a homogenous porous layer of nano-sized magnetite particles immobilized onto granular activated carbon (nFe-GAC) was studied for both interface and bulk structures. X-ray Photoelectron Spectroscopy (XPS) analysis revealed phosphate bonding to the nFe-GAC predominantly through bidentate surface complexes. It was established that phosphate was adsorbed to the magnetite surface mainly via ligand exchange mechanism. Initially, phosphate was adsorbed by the active sites on the magnetite surface, after which it diffused into the interior of the nano-magnetite layer, as indicated by intraparticle diffusion model. This diffusion process continues regardless of interface interactions, revealing some of the outer magnetite binding sites for further phosphate uptake. Desorption, using NaOH solution, was found to be predominantly a surface reaction, at which hydroxyl ions replace the adsorbed phosphate ions only at the surface outer biding sites. Five successive fix-bed adsorption/regeneration cycles were successfully applied, without significant reduction in the nFe-GAC adsorption capacity and at high regeneration efficiency.

MeSH terms

  • Adsorption
  • Ferrosoferric Oxide / chemistry*
  • Membranes, Artificial*
  • Nanostructures / chemistry*
  • Particle Size
  • Phosphates / chemistry*
  • Surface Properties

Substances

  • Membranes, Artificial
  • Phosphates
  • Ferrosoferric Oxide