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High efficient removal of Pb (II) by amino-functionalized Fe3O4 magnetic nano-particles
► Amino-functionalized magnetic nanoparticles were prepared via one-pot method. ► This adsorbent can remove Pb (II) from solution quickly and efficiently. ► The adsorbent can be reused at least 15 times without any significant variation. ► It can remove about 98% of Pb (II) from industrial wastewate...
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Published in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2012-05, Vol.191, p.104-111 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | ► Amino-functionalized magnetic nanoparticles were prepared via one-pot method. ► This adsorbent can remove Pb (II) from solution quickly and efficiently. ► The adsorbent can be reused at least 15 times without any significant variation. ► It can remove about 98% of Pb (II) from industrial wastewater and tap water.
An amino-functionalized magnetic nano-adsorbent (MNPs-NH2) has been prepared by a simple one-pot method for the removal of Pb (II). These amino-functionalized Fe3O4 nano-particles showed a high adsorption capacity and efficient adsorption toward Pb (II) in an aqueous medium. The studies on the adsorption of Pb (II) ions revealed that the process obey the pseudo-second order kinetic model, the determining step might be chemical sorption. Among the various isotherm models, the experimental data for the adsorption of Pb (II) were found to follow the Langmuir isotherm and the maximum adsorption capacity was 40.10mgg−1 at pH 5 and 298K. The sorption mean free energy from the Dubinin–Radushkevich isotherm was found to be 10.31kJmol−1, indicating a chemical sorption. In addition, Pb (II) ions could be desorbed from nano-adsorbents and the MNPs-NH2 exhibited a good reusability. Importantly, about 98% of Pb (II) could be removed by MNPs-NH2 from industrial wastewater and tap water. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2012.02.075 |