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Hierarchical flower-like nickel(II) oxide microspheres with high adsorption capacity of Congo red in water. | LitMetric

Hierarchical flower-like nickel(II) oxide microspheres with high adsorption capacity of Congo red in water.

J Colloid Interface Sci

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Luoshi Road 122, Wuhan 430070, PR China; Department of Physics, Faculty of Science, King Abdulaziz University, Jeddah 21589, Saudi Arabia. Electronic address:

Published: October 2017

AI Article Synopsis

Article Abstract

Monodispersed hierarchical flower-like nickel(II) oxide (NiO) microspheres were fabricated by a facile solvothermal reaction with the assistance of ethanolamine and a subsequent calcination process. The as-synthesized samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, nitrogen adsorption-desorption isotherms, zeta potential measurement and Fourier transform infrared spectroscopy. Flower-like nickel(II) hydroxide microspheres with uniform diameters of approximate 6.3μm were obtained after the solvothermal reaction. After heat treatment at 350°C, the crystal phase transformed to NiO, but the hierarchical porous structure was maintained. The as-prepared microspheres exhibited outstanding performance for the adsorption of Congo red (CR), an anionic organic dye, from aqueous solution at circumneutral pH. The pseudo-second-order model can make a good description of the adsorption kinetics, while Langmuir model could well express the adsorption isotherms, with calculated maximum CR adsorption capacity of 534.8 and 384.6mgg, respectively, for NiO and Ni(OH). The adsorption mechanism of CR onto the as-synthesized samples can be mainly attributed to electrostatic interaction between the positively charged sample surface and the anionic CR molecules. The as-prepared NiO microspheres are a promising adsorbent for CR removal in water treatment.

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Source
http://dx.doi.org/10.1016/j.jcis.2017.06.014DOI Listing

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