Research Articles
Kinetics and isotherm studies for the adsorption of Cu(II) from aqueous solution by carbonbased matrix formed using para-nitroacetanilide
Authors:
T. M. M. K. Bandara ,
University of Peradeniya, Peradeniya, 20400, LK
About T. M. M. K.
Department of Chemistry, Faculty of Science
V. N. Seneviratne
University of Peradeniya, Peradeniya, 20400, LK
About V. N.
Department of Chemistry, Faculty of Science
Abstract
Pollution of water is a pragmatic problem in the world today. Contamination by heavy metals and dyes is a major concern of water pollution. This study examines a new adsorbent made by the reaction between para-nitroacetanilide and concentrated sulfuric acid and is the first-ever study carried out to the best of our knowledge. The adsorption of Cu2+ has been studied on this adsorbent as a preliminary study. The prepared material was characterized using Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), X-ray Fluorescence Spectroscopy (XRF), Powder X-ray Diffraction (PXRD) and point of zero charges (pzc) analysis. The average pore diameter obtained from SEM analysis was 2 μm, concluding that the adsorbent has a desirable morphology for better adsorption. The adsorption experiments were carried out as a function of pH, shaking time, initial Cu2+ concentration, and adsorbent dosage. The adsorption kinetics at low concentrations (34.50 mg L-1 = 1.5 10-7 mol m-3) follows pseudo-second-order kinetics with an R2 value of 0.99, suggesting a chemisorption process. The adsorption data agree with the Freundlich isotherm at higher concentrations (varying from 17.21 mg L-1 (7 10-8 mol m-3) to 96.25 mg L-1 (3.6 10-7 mol m-3) revealing multilayer adsorption, amounting to a maximum adsorption capacity of 8.31 mg g-1 at 250C.
How to Cite:
Bandara, T. M. M. K., & Seneviratne, V. N. (2022). Kinetics and isotherm studies for the adsorption of Cu(II) from aqueous solution by carbonbased matrix formed using para-nitroacetanilide. Ceylon Journal of Science, 51(5), 521–529. DOI: http://doi.org/10.4038/cjs.v51i5.8079
Published on
31 Dec 2022.
Peer Reviewed
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