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1.
Environ Sci Pollut Res Int ; 19(7): 2832-41, 2011 Aug.
Article in English | MEDLINE | ID: mdl-22351255

ABSTRACT

PURPOSE: This work aimed at investigating the adsorption of lead and cadmium onto Fe and Ag nanoparticles for use as a water contaminant removal agent as a function of particle type, sorbent concentration, and contact time. METHODS: Fe and Ag spherical nanoparticles were prepared in water by the lab-made electro-exploding wire (EEW) system and were investigated for their structure properties. Adsorption experiments were carried out at room temperature and pH 8.3 water solutions. RESULTS: The removal/adsorption of both Pb(II) and Cd(II) ions was found to be dependent on adsorbent dosage and contact time. Pb(II) adsorption onto Fe and Ag nanoparticles showed more or less similar efficiency and behavior. The kinetic data for the adsorption process obeyed pseudo second-order rate equations. The calculated equilibrium adsorption capacities (q(e)) were 813 and 800 mg/g for Pb sorption onto Fe and Ag nanoparticles, respectively. Cd(II) ion adsorption onto Fe nanoparticles obeyed pseudo second-order rate equations with q(e) equal to 242 mg/g, while their adsorption onto Ag nanoparticles obeyed pseudo first-order rate equations with q(e) of 794 mg/g. The calculated q(e)s are in quite agreement with the experimental values. The removal/uptake mechanisms of metal ions involved interaction between the metal ion and the oxide/hydroxyl layer around the spherical metallic core of the nanoparticle in water medium. CONCLUSION: Fe and Ag nanoparticles prepared using the EEW technique exhibited high potentials for the removal of metal ions from water with very high adsorption capacities, suggesting that the EEW technique can be enlarged to generate nanoparticles with large quantities for field or site water purification.


Subject(s)
Metal Nanoparticles/chemistry , Metals/chemistry , Water/chemistry , Adsorption , Cadmium/chemistry , Electrochemical Techniques , Iron/chemistry , Lead/chemistry , Silver/chemistry , Time Factors , Water Pollutants, Chemical/chemistry , Water Purification/methods
2.
J Nanosci Nanotechnol ; 7(6): 1898-903, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17654962

ABSTRACT

Nanoparticles of iron were prepared in distilled water using very thin iron wires and sheets, by the electro-exploding wire technique. Transmission electron microscopy reveals the size of the nanoparticles to be in the range 10 to 50 nm. However, particles of different sizes can be segregated by using ultrahigh centrifuge. X-ray diffraction studies confirm the presence of the cubic phase of iron. These iron nanoparticles were found to exhibit fluorescence in the visible region in contrast to the normal bulk material. The room temperature hysteresis measurements upto a field of 1.0 tesla were performed on a suspension of iron particles in the solution as well as in the powders obtained by filtration. The hysteresis loops indicate that the particles are superparamagnetic in nature. The saturation magnetizations was approximately 60 emu/gm. As these iron particles are very sensitive to oxygen a coating of non-magnetic iron oxide tends to form around the particles giving it a core-shell structure. The core particle size is estimated theoretically from the magnetization measurements. Suspensions of iron nanoparticles in water have been proposed to be used as an effective decontaminant for ground water.


Subject(s)
Crystallization/methods , Iron/chemistry , Nanostructures/chemistry , Nanostructures/ultrastructure , Nanotechnology/methods , Macromolecular Substances/chemistry , Magnetics , Materials Testing , Molecular Conformation , Particle Size , Surface Properties
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