Nanocrystalline Akaganeite as Adsorbent for Surfactant Removal from Aqueous Solutions.

The present study presents the effective use of nanocrystalline akaganeite for the adsorption of an anionic (SDS), a cationic (CTAB), and a nonionic (tween80) surfactant from wastewater. Equilibrium experiments, as well as thermodynamic analysis, were performed. The maximum SDS adsorption occurs at the lowest pH value (5), the opposite is observed for CTAB (pH = 11), while for tween80, the change of pH value did not affect the adsorption. The equilibrium data could be described by Freundlich and Langmuir isotherms. The maximum adsorption capacity at 25 °C (pH = 8) was 823.96 mg/g for SDS, 1007.93 mg/g for CTAB, and 699.03 mg/g for tween80. The thermodynamic parameters revealed the exothermic and spontaneity nature of the process. Also, FTIR measurements established that surfactants are adsorbed on the surface of akaganeite, replacing adsorbed water.

Iron-modified hydrotalcite-like materials as highly efficient phosphate sorbents.

Highly efficient sorbents for phosphate removal from aqueous solutions based on the calcined forms of Fe(III)-substituted Layered Double Hydroxides (LDH) materials have been developed in this study. Hydrotalcite-like materials with Mg/M(3+) approximately 3 (where M=Al(3+), Fe(3+) or combined) have been synthesized following simple co-precipitation method and were subsequently calcined in air at 450 degrees C. Both as-synthesized and calcined materials were characterized by means of X-ray Diffraction (XRD), Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES), elemental (C) analysis, N(2) porosimetry, Scanning Electron Microscopy (SEM). All the materials were evaluated for the sorption of phosphates by batch equilibrium sorption experiments and kinetic measurements (effect of contact time). It was shown that chlorides or nitrates, being the charge-balancing anions in the LDH structure, are more easily exchanged by phosphates compared to carbonates. In the Fe(III)-modified LDHs, an increase of the Fe loading led to the decrease of the sorption efficiency. The maximum uptake of phosphates for both the Mg-Al LDH and Mg-Fe LDH samples containing mainly carbonates as charge-balancing anions was relatively low (ca.