Preparation of high surface area activated carbon from waste-biomass of sunflower piths: Kinetics and equilibrium studies on the dye removal
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Accepted version
Author(s)
Baysal, M
Bilge, K
Yilmaz, B
Papila, M
Yurum, Y
Type
Journal Article
Abstract
Sunflower pith (SP), a vast agricultural waste is herein used as a precursor material for highly porous low density activated carbon production. Porosity and flake-like microstructure of the SP in its natural form are shown by micro-computed tomography (Micro-CT). Carbonization process turns the SP into thin, separated carbon flakes of 200 nm thickness. Two types of alkaline based chemical activation with KOH and NaOH are performed to yield SP based activated carbon (AC), K-SPAC and N-SPAC, respectively. Microstructural changes upon carbonization and activation process are elaborated by RAMAN, FTIR and SEM analyses. BET Surface area of the NaOH-activated N-SPAC was calculated as 2690 m2/g and was higher than KOH-activated K-SPAC with 2090 m2/g. Maximum adsorption capacity of N-SPAC was calculated as 965 mg/g whereas it was 580 mg/g for K-SPAC. Adsorption kinetic studies for N-SPAC revealed that at a low initial concentration of dye (500 mg/L), the pseudo first-order kinetic model was predictive. On the other hand, at high initial MB concentration (1000 mg/L), the results indicate that the adsorption kinetics follow the Elovich model with intraparticle diffusion as one of the rate-determining steps.
In conclusion, overall results suggest that thanks to its highly porous microstructure, the SP is an alternative renewable AC precursor choice for dye removal applications.
In conclusion, overall results suggest that thanks to its highly porous microstructure, the SP is an alternative renewable AC precursor choice for dye removal applications.
Date Issued
2018-04-01
Date Acceptance
2018-02-12
Citation
Journal of Environmental Chemical Engineering, 2018, 6 (2), pp.1702-1713
ISSN
2213-3437
Publisher
Elsevier
Start Page
1702
End Page
1713
Journal / Book Title
Journal of Environmental Chemical Engineering
Volume
6
Issue
2
Copyright Statement
© 2018, Elsevier. Licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/
Publication Status
Published
Date Publish Online
2018-02-13