This study presents the results of synthesis and characterization of nanoparticles of cobalt ferrite (CoFeO) and nickel ferrite (NiFeO) using co-precipitation method followed by application for removal of hazardous organic textile dyes of thiazole yellow G (TYG) and alizarin yellow R (AYR). XRD analysis confirmed formation of cubic spinel structure with average crystallite sizes at 16.07 nm and 13.84 nm for CoFeO and NiFeO, respectively. Field emission scanning electron microscopy (FESEM) analysis showed agglomeration of spherical shape morphology with uniformly distributed Co, Ni, Fe, and O elements. The surface area calculated from Brunauer-Emmett-Teller (BET) analysis was 64 m/g and 62 m/g for CoFeO and NiFeO, respectively. Vibrating sample magnetometer (VSM) showed super-paramagnetic behavior for all samples with magnetic saturation (M) at 7.269 and 6.61 emu/g for CoFeO and NiFeO, respectively. The adsorption influencing parameters such as pH of solution, quantity of adsorbent, and contact time on dye removal efficiency were thoroughly investigated. Overall, acidic condition of samples with pH at 4 favored the maximum removal efficiency by CoFeO as 98, 97, and 93%, and by NiFeO as 96, 93, and 92%, respectively, for TYG, AYR, and mixture sample. The Langmuir adsorption isotherm model describes the equilibrium of all samples with the best fit of coefficient of determination (R). The adsorption results fitted well with a pseudo-second-order kinetic model for all samples. The regeneration-reuse ability of adsorbents and cost estimation analysis of the dye removal process suggested that the economic suitability of nano-adsorbents for remediation of textile effluents was favored. The estimated thermodynamic parameters inferred that the removal of organic dyes onto the surface of CoFeO and NiFeO is a spontaneous, favorable, and exothermic physical adsorption process.
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http://dx.doi.org/10.1007/s11356-023-26059-5 | DOI Listing |
J Am Chem Soc
November 2013
Joint Center for Artificial Photosynthesis and †Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States.
Objective evaluation of the activity of electrocatalysts for water oxidation is of fundamental importance for the development of promising energy conversion technologies including integrated solar water-splitting devices, water electrolyzers, and Li-air batteries. However, current methods employed to evaluate oxygen-evolving catalysts are not standardized, making it difficult to compare the activity and stability of these materials. We report a protocol for evaluating the activity, stability, and Faradaic efficiency of electrodeposited oxygen-evolving electrocatalysts.
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