Efficient removal of organic dyestuff in water contamination over a MOF-derived Co-based adsorbent
In this study, we developed an adsorption technology by using MOF-derived Co-based adsorbents for the efficient removal of organic dyestuff (rhodamine B) solutions. The maximum adsorption capacity of rhodamine B in an hour over Co 0.5 (PTA)@C (the Co-based adsorbent with the best Co/terephthalic aci...
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Published in | Reaction chemistry & engineering Vol. 8; no. 9; pp. 2195 - 2210 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
22.08.2023
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Subjects | |
Online Access | Get full text |
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Summary: | In this study, we developed an adsorption technology by using MOF-derived Co-based adsorbents for the efficient removal of organic dyestuff (rhodamine B) solutions. The maximum adsorption capacity of rhodamine B in an hour over Co
0.5
(PTA)@C (the Co-based adsorbent with the best Co/terephthalic acid molar ratio of 1 : 2) was 336.73 mg g
−1
, indicating that the adsorbent was promising for dye wastewater adsorption and could be widely used in practical wastewater applications. The adsorbents with different metals (Ni, Fe, Cu, and Co), ligands (trimesic acid and terephthalic acid), and metal/ligand molar ratios were evaluated and characterized by XRD, SEM, TEM, HRTEM, BET, ICP and XPS analyses. The potential mechanism of adsorption and the adsorption kinetic behavior were investigated using pseudo-first-order and pseudo-second-order kinetic models, and the experimental data were analyzed by employing Langmuir and Freundlich adsorption isotherms for assessing the adsorption processes and equilibrium properties.
An adsorption technology was developed by using a MOF-derived Co-based adsorbent for the efficient removal of organic dyestuff (RhB) solutions from water combined with a hydrothermal method and a carbonization technique. |
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Bibliography: | https://doi.org/10.1039/d3re00126a Electronic supplementary information (ESI) available. See DOI |
ISSN: | 2058-9883 2058-9883 |
DOI: | 10.1039/d3re00126a |