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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Majdi, Hasan Sh.
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- 2024Performance Analysis of Motor Vibration Based Condition Monitoring Using R-curve
- 2023Adsorption of aniline from aqueous solutions onto a nanoporous material adsorbent: isotherms, kinetics, and mass transfer mechanismscitations
- 2022An in-depth analysis of nucleation and growth mechanism of CdS thin film synthesized by chemical bath deposition (CBD) techniquecitations
- 2022Pyramidal Solar Stills via Hollow Cylindrical Perforated Fins, Inclined Rectangular Perforated Fins, and Nanocomposites: An Experimental Investigationcitations
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article
Adsorption of aniline from aqueous solutions onto a nanoporous material adsorbent: isotherms, kinetics, and mass transfer mechanisms
Abstract
<jats:title>Abstract</jats:title><jats:p>MCM-48, which is particulate and nanoporous, was formulated to actively remove aniline (AN) (i.e., benzenamine) from wastewater. MCM-48 was characterized by several methods. It was found that the MCM-48 was highly active in adsorbing aniline from wastewater. The Langmuir, Freundlich, and Temkin isotherms were employed to evaluate the adsorption equilibrium. At 100 and 94 mg g−1, the maximum theoretical and experimental absorption of aniline, respectively, fit with a Type I Langmuir isotherm. The Langmuir model was optimal in comparison to the Freundlich model for the adsorption of AN onto the mesoporous material MCM-48. The results of these kinetics adsorption models were investigated using model kinetics that employed both pseudo-first- and pseudo-second-order models as well as models utilized intraparticle diffusion. The kinetics adsorption models demonstrated that the absorption was rapid and most closely agreed with the pseudo-first-order model. The kinetic studies and the adsorption isotherms revealed the presence of both physical adsorption and chemisorption. The potential adsorption mechanisms include the following: (1) hydrogen bonding, (2) π-π interactions, (3) electrostatic interaction, and (4) hydrophobic interactions. The solution's pH, ionic strength, and ambient temperature also played essential roles in the adsorption.</jats:p>