Adsorption of congo red and methylene blue dyes on an ashitaba waste and a walnut shell-based activated carbon from aqueous solutions: Experiments, characterization and physical interpretations

Activated carbons were prepared from ashitaba waste and a walnut shell to study the adsorption mechanism of congo red and methylene blue dyes in aqueous solution. These adsorbents were characterized via XRD, FTIR and SEM techniques and the dye adsorption isotherms at three temperatures were quantifi...

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Autores:
Li, Zichao
Hanafy, Hassan
Zhanga, Lei
Sellaouid, Lotfi
Schadeck Netto, Matias
Silva Oliveira, Marcos Leandro
Seliem, Moaaz K.
Dotto, Guilherme Luiz
Bonilla-Petriciolet, Adrian
Lia, Qun
Tipo de recurso:
http://purl.org/coar/resource_type/c_816b
Fecha de publicación:
2020
Institución:
Corporación Universidad de la Costa
Repositorio:
REDICUC - Repositorio CUC
Idioma:
eng
OAI Identifier:
oai:repositorio.cuc.edu.co:11323/5971
Acceso en línea:
http://hdl.handle.net/11323/5971
https://repositorio.cuc.edu.co/
Palabra clave:
Ashitaba waste
Walnut Shell
Methylene blue
Congo red
Physical modeling
Activated carbon
Rights
openAccess
License
CC0 1.0 Universal
Description
Summary:Activated carbons were prepared from ashitaba waste and a walnut shell to study the adsorption mechanism of congo red and methylene blue dyes in aqueous solution. These adsorbents were characterized via XRD, FTIR and SEM techniques and the dye adsorption isotherms at three temperatures were quantified. A statistical physics model was applied to interpret the adsorption mechanism of tested dyes and adsorbents. Modeling results showed that these dyes were practically separated in the solution leading to an absence of the aggregation process. Adsorption orientations of dye molecules on the adsorbents changed depending on the temperature and nature of systems. The adsorption capacity of ashitaba waste activated carbon for the removal of congo red was significant thus indicating strong interactions between this dye and tested adsorbent. Calculated adsorption energy varied from 7.25 to 20.43 kJ/mol and they showed that the adsorption of both adsorbates occurred via physical interactions at different temperatures where the removal process was endothermic.