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Multifunctional nanocomposite Fe3O4@SiO2–mPD/SP for selective removal of Pb(<scp>ii</scp>) and Cr(<scp>vi</scp>) from aqueous solutions
- Source :
- RSC Adv.. 4:45920-45929
- Publication Year :
- 2014
- Publisher :
- Royal Society of Chemistry (RSC), 2014.
-
Abstract
- Silica-coated magnetite (Fe3O4@SiO2) nanoparticles functionalized with amino, imino and sulfonic groups (Fe3O4@SiO2–mPD/SP) were successfully synthesized via a facile chemical oxidative polymerization of m-phenylenediamine (mPD) and m-sulfophenylenediamine-4-sulfonic acid (SP) monomers, and utilized for selective removal of Pb(II) and Cr(VI) from aqueous solutions. It was revealed by the characterizations that the polymers formed on Fe3O4@SiO2 nanoparticles were the true copolymers with a mPD–SP unit, rather than a mixture of mPD and SP homopolymers. Fe3O4@SiO2–mPD/SP nanocomposites could be easily separated from aqueous solutions within 30 s. The maximum adsorption capacities of Pb(II) (83.23 mg g−1) and Cr(VI) (119.06 mg g−1) on Fe3O4@SiO2–mPD/SP nanocomposites were obtained at the mPD/SP molar ratios of 95 : 5 and 50 : 50, respectively. Moreover, satisfactory selective removal of Pb(II) and Cr(VI) from their mixtures with Cu(II) and Ni(II) ions were exhibited by the Fe3O4@SiO2–mPD/SP (95 : 5) and Fe3O4@SiO2–mPD/SP (50 : 50), respectively. The Pb(II) adsorption equilibrium was reached within 5 min by Fe3O4@SiO2–mPD/SP (95 : 5). The adsorption data of Pb(II) and Cr(VI) were both fitted well to the Freundlich isotherm and followed the pseudo-second-order kinetic model. The adsorption mechanism of Pb(II) and Cr(VI) on Fe3O4@SiO2–mPD/SP nanocomposites included five processes, namely: ion-exchange, complexation adsorption, reduction reaction, electrostatic attraction and physical adsorption. The enhanced adsorption performance of nanoparticle-based magnetic adsorbents for selective removal of heavy metal ions can be achieved with such a copolymerization strategy.
Details
- ISSN :
- 20462069
- Volume :
- 4
- Database :
- OpenAIRE
- Journal :
- RSC Adv.
- Accession number :
- edsair.doi...........6ff459fa090e901d912c3726f76664eb