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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received March 27, 2020
Accepted June 30, 2020
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Single and binary adsorption of dyes from aqueous solutions using functionalized microcrystalline cellulose from cotton fiber

Province Key Laboratory of Cereal Resource Transformation and Utilization, School of Chemistry and Chemical Engineering, Henan University of Technology, Zhengzhou 450001, P. R. China
chenjunhang@haut.edu.cn
Korean Journal of Chemical Engineering, November 2020, 37(11), 1926-1932(7), 10.1007/s11814-020-0621-3
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Abstract

Simultaneous removal of dyes in the effluents of printing and dyeing industries is challenging, and the mechanism of the co-adsorption of dyes is still unclear. In this context, a novel adsorbent based on microcrystalline cellulose from cotton fiber through a simplified chemical modification process was prepared. Methylene blue (MB) and neutral red (NR) were selected to investigate their adsorption/co-adsorption on such functionalized microcrystalline cellulose. The experimental adsorption results indicated that the adsorption quantity of both dyes was similar for the single solute. The kinetics of adsorption processes could be better described with the pseudo-second order models for both single and binary dye solutes. The results of the co-adsorption suggested that the extended Langmuir model could well predict equilibrium. The maximum adsorption capacity of MB and NR for the single systems was 115.2 and 83.2mg/g, respectively. Moreover, an antagonistic effect could be found in the binary dye solute. The obtained results revealed that the co-adsorption of dyes might be driven by hydrogen bonding, π-π stacking interaction as well as electrostatic interaction.

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