RESUMO
Lead (Pb) ions are a major concern to the environment and human health as they are contemplated cumulative poisons. In this study, facile synthesis of magnetic iron oxide-tea waste nanocomposite is reported for adsorptive removal of lead ions from aqueous solutions and easy magnetic separation of the adsorbent afterwards. The samples were characterised by scanning electron microscopy, Fourier transform-infrared spectroscopy, X-ray diffraction, and Braunner-Emmet-Teller nitrogen adsorption study. Adsorptive removal of Pb(II) ions from aqueous solution was followed by ultraviolet-visible (UV-Vis) spectrophotometry. About 95% Pb(II) ion removal is achieved with the magnetic tea waste within 10â min. A coefficient of regression R2 ≃ 0.99 and adsorption density of 18.83â mgâ g-1 was found when Pb(II) ions were removed from aqueous solution using magnetic tea waste. The removal of Pb(II) ions follows the pseudo-second-order rate kinetics. External mass transfer principally regulates the rate-limiting phenomena of adsorption of Pb(II) ions on iron oxide-tea waste surface. The results strongly imply that magnetic tea waste has promising potential as an economic and excellent adsorbent for the removal of Pb(II) from water.
Assuntos
Chumbo , Nanopartículas de Magnetita/química , Nanocompostos/química , Águas Residuárias/química , Poluentes Químicos da Água , Adsorção , Íons/química , Íons/isolamento & purificação , Íons/metabolismo , Cinética , Chumbo/química , Chumbo/isolamento & purificação , Chumbo/metabolismo , Chá , Poluentes Químicos da Água/química , Poluentes Químicos da Água/isolamento & purificação , Poluentes Químicos da Água/metabolismoRESUMO
Substituting an ion of different size from that of the host element introduces lattice strain and defects. However, this mismatch may be significantly reduced by substituting an additional ion with a compensating size relative to the dopant. Such a double substitution might offer better solubility irrespective of the local distortions as well as the formation of defects in the valence states. Fe-substituted ZnO has been widely reported with conflicting results primarily arising from lack of chemical and structural homogeneity originating from preparation techniques, compositional fluctuations, and equivocal comprehension of actual solubility limits of the dopants. In this study, Ag ion has been incorporated in Fe-substituted ZnO to compensate the ionic size of Zn1-x [Fe0.8Ag0.2] x O (0 ≤ x ≤ 0.03125) by determining the solubility limit of the homogeneous material and their corresponding structural, mechanical, optical and magnetic properties have been investigated thoroughly. Co-substitution rearranges the lattice and leads to better crystal structures with tunable properties related to the amount of substitution.
RESUMO
[This corrects the article DOI: 10.1039/C8RA02393J.].