Understanding the Cu2+ adsorption mechanism on activated carbon using advanced statistical physics modelling

Adsorption modeling via statistical physics theory allows to understand the adsorption mechanism of heavy metal ions. Therefore, this paper reports the analysis of the mechanism of copper ion (Cu2+) adsorption on four activated carbons using statistical physics models. These models contain parameter...

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Autores:
Sellaoui, Lotfi
Dhaouadi, Fatma
sonia, taamalli
Louis, Florent
Abderrahman, El Bakali
Badawi, Michael
Bonilla-Petriciolet, Adrian
Silva Oliveira, Luis Felipe
da Boit Martinello, Kátia
Dotto, Guilherme Luiz
Ben Lamine, Abdemottaleb
Tipo de recurso:
Article of journal
Fecha de publicación:
2022
Institución:
Corporación Universidad de la Costa
Repositorio:
REDICUC - Repositorio CUC
Idioma:
eng
OAI Identifier:
oai:repositorio.cuc.edu.co:11323/9168
Acceso en línea:
https://hdl.handle.net/11323/9168
https://doi.org/10.1007/s11356-022-19795-7
https://repositorio.cuc.edu.co/
Palabra clave:
Adsorption
Cooper
Isotherms
Statistical physics
Rights
embargoedAccess
License
© 2022 Springer Nature Switzerland AG. Part of Springer Nature.
Description
Summary:Adsorption modeling via statistical physics theory allows to understand the adsorption mechanism of heavy metal ions. Therefore, this paper reports the analysis of the mechanism of copper ion (Cu2+) adsorption on four activated carbons using statistical physics models. These models contain parameters that were utilized to provide new insights into the possible adsorption mechanism at the molecular scale. In particular, a monolayer adsorption model was the best alternative to correlate the Cu2+ adsorption data at 25–55 °C and pH 5.5. Furthermore, the application of this model for copper adsorption data analysis showed that the removal of this heavy metal ion was a multi-cationic process. This theoretical finding indicated that Cu2+ ions interacted via one functional group of activated carbon surface during adsorption. In this direction, the adsorption energy was calculated thus showing that Cu2+ removal was endothermic and associated with physical interaction forces. Furthermore, these activated carbons showed saturation adsorption capacities from 54.6 to 87.0 mg/g for Cu2+ removal, and their performances outperformed other adsorbents available in the literature. Overall, these results provide new insights of the adsorption mechanism of this water pollutant using activated carbons.