Optimization and mechanistic insight of phenol removal using an effective green kaolin adsorbent through experimental and computational approaches

The discharge of phenols into the aquatic environment has detrimentally affected human health and the aquatic ecosystem. Hence, removing phenols from polluted water bodies has been a global concern. In this study, a natural and low-cost adsorbent, kaolin, was used to remove phenol from aqueous solut...

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Main Authors: Zubir, Aisyah, Erna Normaya, Erna Normaya, Zuhaidi, Nurul Huda, Goh, Pei Sean, Mat Piah, Mohd. Bijarimi, Ismail, Mohamad Wafiuddin, Show, Pau Loke, Ismail, Ahmad Fauzi, Ahmad, Mohammad Norazmi
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Published: Elsevier B.V. 2024
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Online Access:http://eprints.utm.my/108901/
http://dx.doi.org/10.1016/j.molstruc.2024.139219
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spelling my.utm.1089012024-12-11T09:47:29Z http://eprints.utm.my/108901/ Optimization and mechanistic insight of phenol removal using an effective green kaolin adsorbent through experimental and computational approaches Zubir, Aisyah Erna Normaya, Erna Normaya Zuhaidi, Nurul Huda Goh, Pei Sean Mat Piah, Mohd. Bijarimi Ismail, Mohamad Wafiuddin Show, Pau Loke Ismail, Ahmad Fauzi Ahmad, Mohammad Norazmi Q Science (General) The discharge of phenols into the aquatic environment has detrimentally affected human health and the aquatic ecosystem. Hence, removing phenols from polluted water bodies has been a global concern. In this study, a natural and low-cost adsorbent, kaolin, was used to remove phenol from aqueous solutions. Experimental and computational approaches were applied to optimize the removal efficiency and provide mechanistic insight into the phenol removal process. Based on the response surface methodology findings, the optimum conditions were pH 1.6, 40 min, 50 mg/L, and 2 g with 92.19 % maximum percentage removal. The regeneration test shows that kaolin retained over 76.76 % of adsorption capacities. SEM and FESEM reveals the surface morphology and effectiveness of kaolin as phenol removal. The best fit for the Isotherm adsorption for the phenol on kaolin is Freundlich isotherm, which indicated multilayer adsorption. The hydroxyl group from phenol (-OH) and the siloxane group of kaolin (Si-O-Si) shifted, suggesting the presence of a hydrogen bond between kaolin and phenol during adsorption, as determined by one- and two-dimensional IR spectroscopy. Density functional theory calculations were used to support the experimental results by providing information on the Mulliken charge and electronic transition of the complex to improve understanding of the adsorption of phenol on kaolin. Based on the quantum theory of atoms in molecules analysis (QTAIM) and the reduced density gradient non-covalent interaction (RDG-NCI) technique, the chemical reaction occurring during the removal of phenol by kaolin was determined to occur through hydrogen bonding and classified as an intermediate type (∇2ρ(r) > 0 and H < 0). Further characterizations employing molecular electrostatic potential, global reactivity, and local reactivity descriptors were conducted to investigate the mechanism of the phenol adsorption on kaolin. The findings demonstrated that phenol functions as an electrophile while kaolin acts as a nucleophile during the formation of hydrogen bonds, where the interaction occurred between the O2 atom of kaolin (electron donor) and the H13 atom of phenol (electron acceptor). Elsevier B.V. 2024-12 Article PeerReviewed Zubir, Aisyah and Erna Normaya, Erna Normaya and Zuhaidi, Nurul Huda and Goh, Pei Sean and Mat Piah, Mohd. Bijarimi and Ismail, Mohamad Wafiuddin and Show, Pau Loke and Ismail, Ahmad Fauzi and Ahmad, Mohammad Norazmi (2024) Optimization and mechanistic insight of phenol removal using an effective green kaolin adsorbent through experimental and computational approaches. Journal of Molecular Structure, 1318 (NA). NA. ISSN 0022-2860 http://dx.doi.org/10.1016/j.molstruc.2024.139219 DOI:10.1016/j.molstruc.2024.139219
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic Q Science (General)
spellingShingle Q Science (General)
Zubir, Aisyah
Erna Normaya, Erna Normaya
Zuhaidi, Nurul Huda
Goh, Pei Sean
Mat Piah, Mohd. Bijarimi
Ismail, Mohamad Wafiuddin
Show, Pau Loke
Ismail, Ahmad Fauzi
Ahmad, Mohammad Norazmi
Optimization and mechanistic insight of phenol removal using an effective green kaolin adsorbent through experimental and computational approaches
description The discharge of phenols into the aquatic environment has detrimentally affected human health and the aquatic ecosystem. Hence, removing phenols from polluted water bodies has been a global concern. In this study, a natural and low-cost adsorbent, kaolin, was used to remove phenol from aqueous solutions. Experimental and computational approaches were applied to optimize the removal efficiency and provide mechanistic insight into the phenol removal process. Based on the response surface methodology findings, the optimum conditions were pH 1.6, 40 min, 50 mg/L, and 2 g with 92.19 % maximum percentage removal. The regeneration test shows that kaolin retained over 76.76 % of adsorption capacities. SEM and FESEM reveals the surface morphology and effectiveness of kaolin as phenol removal. The best fit for the Isotherm adsorption for the phenol on kaolin is Freundlich isotherm, which indicated multilayer adsorption. The hydroxyl group from phenol (-OH) and the siloxane group of kaolin (Si-O-Si) shifted, suggesting the presence of a hydrogen bond between kaolin and phenol during adsorption, as determined by one- and two-dimensional IR spectroscopy. Density functional theory calculations were used to support the experimental results by providing information on the Mulliken charge and electronic transition of the complex to improve understanding of the adsorption of phenol on kaolin. Based on the quantum theory of atoms in molecules analysis (QTAIM) and the reduced density gradient non-covalent interaction (RDG-NCI) technique, the chemical reaction occurring during the removal of phenol by kaolin was determined to occur through hydrogen bonding and classified as an intermediate type (∇2ρ(r) > 0 and H < 0). Further characterizations employing molecular electrostatic potential, global reactivity, and local reactivity descriptors were conducted to investigate the mechanism of the phenol adsorption on kaolin. The findings demonstrated that phenol functions as an electrophile while kaolin acts as a nucleophile during the formation of hydrogen bonds, where the interaction occurred between the O2 atom of kaolin (electron donor) and the H13 atom of phenol (electron acceptor).
format Article
author Zubir, Aisyah
Erna Normaya, Erna Normaya
Zuhaidi, Nurul Huda
Goh, Pei Sean
Mat Piah, Mohd. Bijarimi
Ismail, Mohamad Wafiuddin
Show, Pau Loke
Ismail, Ahmad Fauzi
Ahmad, Mohammad Norazmi
author_facet Zubir, Aisyah
Erna Normaya, Erna Normaya
Zuhaidi, Nurul Huda
Goh, Pei Sean
Mat Piah, Mohd. Bijarimi
Ismail, Mohamad Wafiuddin
Show, Pau Loke
Ismail, Ahmad Fauzi
Ahmad, Mohammad Norazmi
author_sort Zubir, Aisyah
title Optimization and mechanistic insight of phenol removal using an effective green kaolin adsorbent through experimental and computational approaches
title_short Optimization and mechanistic insight of phenol removal using an effective green kaolin adsorbent through experimental and computational approaches
title_full Optimization and mechanistic insight of phenol removal using an effective green kaolin adsorbent through experimental and computational approaches
title_fullStr Optimization and mechanistic insight of phenol removal using an effective green kaolin adsorbent through experimental and computational approaches
title_full_unstemmed Optimization and mechanistic insight of phenol removal using an effective green kaolin adsorbent through experimental and computational approaches
title_sort optimization and mechanistic insight of phenol removal using an effective green kaolin adsorbent through experimental and computational approaches
publisher Elsevier B.V.
publishDate 2024
url http://eprints.utm.my/108901/
http://dx.doi.org/10.1016/j.molstruc.2024.139219
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