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Zain Al-Abidine Naji Al-Hasnawy Khawla Kani Jasim Masar Ali Awad

Abstract

In the present study, ZnFe2O4 nanoparticles were synthesized using an ultrasound- assisted Co-precipitation method and ZnFe2O4-PANI-GO nanocomposite was synthesized by in situ oxidative polymerization to form a three-dimensional network structure. The characterization of prepared nanomaterials was done through different techniques such as X-ray diffraction (XRD), Field Emission Scanning Electron Microscope (FE-SEM), elemental analyses (EDS & elemental mapping), Vibrating-Sample Magnetometer (VSM), Surface area analysis (BET & BJH), Fourier Transform Infrared Spectroscopy (FT-IR), Atomic Force Microscope (AFM), and thermogravimetric analysis (TGA). PANI, GO, and ZnFe2O4 ternary nanomaterials are wrapped together to form a three-dimensional porous nanostructure and homogeneously dispersed according to the EDS, elemental mapping, and FE-SEM images. The FT-IR Spectroscopy exhibits the emergence and shifts in the main bands and in addition XRD which the average it's crystal sizes (19.35 nm) for ZnFe2O4-PANI-GO are different from ZnFe2O4. Moreover, ZnFe2O4-PANI-GO was studied as an adsorbent to show (OG and MG dyes) adsorption from an aqueous solution. Thermodynamic factors (∆G°, ∆H°, and ∆S°) concluded that the adsorption of both dyes was spontaneous in nature and exothermic. The adsorption pursued pseudo-second-order kinetics. In addition, the isotherm models Freundlich, Langmuir, and Timken were used to model the experimental adsorption data. To match the experimental isotherm, the Langmuir isotherm was utilized.

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Keywords

Nanocomposite, Zinc ferrite, Polyaniline, Graphene oxide, Adsorption, Water treatment

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