Selective Removal of Heavy Metals from Industrial Wastewater Using Maghemite Nanoparticle: Performance and Mechanisms

• Published in: Journal of environmental engineering (New York, N.Y.) Vol. 132; no. 7; pp. 709 - 715
• Main Authors: Hu, Jing, Chen, Guohua, Lo, Irene M. C
• Format: Journal Article
• Language: English
• Published: Reston, VA American Society of Civil Engineers 01.07.2006
• Subjects: Applied sciences; Exact sciences and technology; General purification processes; Other industrial wastes. Sewage sludge; Pollution; TECHNICAL PAPERS; Wastes; Wastewaters; Water treatment and pollution; Nanoparticle; Adsorption isotherm; Metallurgical industry; Desorption; X ray diffraction; Langmuir isotherm; Heavy metals; Waste water; Heavy metal; Industrial water; Industrial waste; Transmission electron microscopy; Adsorption; Batchwise; Industrial wastes; Industrial waste water; pH; Electrodeposition; Kinetics; Surface area; Ion exchange
• ISSN: 0733-9372; 1943-7870
• DOI: 10.1061/(ASCE)0733-9372(2006)132:7(709)

This study investigated the applicability of maghemite (γ- Fe2 O3 ) nanoparticles for the selective removal of toxic heavy metals from electroplating wastewater. The maghemite nanoparticles of 10 nm were synthesized using a sol–gel method and characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The surface area of the nanoparticles was determined to be 198 m2 ∕g using the Brunauer–Emmett–Teller method. Batch experiments were carried out to determine the adsorption kinetics and mechanisms of Cr(VI) , Cu(II) , and Ni(II) by maghemite nanoparticles. The adsorption process was found to be highly pH dependent, which made the nanoparticles selectively adsorb these three metals from wastewater. The adsorption of heavy metals reached equilibrium rapidly within 10 min and the adsorption data were well fitted with the Langmuir isotherm. Regeneration studies indicated that the maghemite nanoparticles undergoing successive adsorption–desorption processes retained original metal removal capacity. Mechanism studies using TEM, XRD, and X-ray photoelectron spectroscopy suggested that the adsorption of Cr(VI) and Cu(II) could be due to electrostatic attraction and ion exchange, and the adsorption of Ni(II) could be as a result of electrostatic attraction only.