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Selectivity of Sol-Gel and Hydrothermal TiO(2) Nanoparticles towards Photocatalytic Degradation of Cationic and Anionic Dyes

Titanium dioxide (TiO(2)) nanoparticles have been extensively studied for catalyzing the photo-degradation of organic pollutants, the photocatalyst being nonselective to the substrate. We, however, found that TiO(2) nanoparticles prepared via the sol-gel and hydrothermal synthetic routes each posses...

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Autores principales: Islam, Md. Torikul, Roni, Md. Nahid Parvez, Ali, Md. Yunus, Islam, Md. Robiul, Hossan, Md. Shamim, Rahman, M. Habibur, Zahid, A. A. S. Mostofa, Alam, Md. Nur E, Hanif, Md. Abu, Akhtar, M. Shaheer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574600/
https://www.ncbi.nlm.nih.gov/pubmed/37836678
http://dx.doi.org/10.3390/molecules28196834
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author Islam, Md. Torikul
Roni, Md. Nahid Parvez
Ali, Md. Yunus
Islam, Md. Robiul
Hossan, Md. Shamim
Rahman, M. Habibur
Zahid, A. A. S. Mostofa
Alam, Md. Nur E
Hanif, Md. Abu
Akhtar, M. Shaheer
author_facet Islam, Md. Torikul
Roni, Md. Nahid Parvez
Ali, Md. Yunus
Islam, Md. Robiul
Hossan, Md. Shamim
Rahman, M. Habibur
Zahid, A. A. S. Mostofa
Alam, Md. Nur E
Hanif, Md. Abu
Akhtar, M. Shaheer
author_sort Islam, Md. Torikul
collection PubMed
description Titanium dioxide (TiO(2)) nanoparticles have been extensively studied for catalyzing the photo-degradation of organic pollutants, the photocatalyst being nonselective to the substrate. We, however, found that TiO(2) nanoparticles prepared via the sol-gel and hydrothermal synthetic routes each possess a definite specificity to the charge of the substrate for photodegradation. The nanoparticles were characterized by SEM, FTIR, XRD, TGA, and UV-visible spectra, and the photocatalytic degradation under UV-B (285 nm) irradiation of two model compounds, anionic methyl Orange (MO) and cationic methylene blue (MB) was monitored by a UV-visible spectrophotometer. Untreated sol-gel TiO(2) nanoparticles (T(sg)) preferentially degraded MO over MB (90% versus 40% in two hours), while after calcination at 400 °C for two hours (T(sgc)) they showed reversed specificity (50% MO versus 90% MB in one hour). The as-prepared hydrothermal TiO(2) nanoparticles (T(ht)) behaved in the opposite sense of T(sg) (41% MO versus 91% MB degraded in one and a half hours); calcination at 400 °C (T(htc)) did not reverse the trend but enhanced the efficiency of degradation. The study indicates that TiO(2) nanoparticles can be made to degrade a specific class of organic pollutants from an effluent facilitating the recycling of a specific class of pollutants for cost-effective effluent management.
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spelling pubmed-105746002023-10-14 Selectivity of Sol-Gel and Hydrothermal TiO(2) Nanoparticles towards Photocatalytic Degradation of Cationic and Anionic Dyes Islam, Md. Torikul Roni, Md. Nahid Parvez Ali, Md. Yunus Islam, Md. Robiul Hossan, Md. Shamim Rahman, M. Habibur Zahid, A. A. S. Mostofa Alam, Md. Nur E Hanif, Md. Abu Akhtar, M. Shaheer Molecules Article Titanium dioxide (TiO(2)) nanoparticles have been extensively studied for catalyzing the photo-degradation of organic pollutants, the photocatalyst being nonselective to the substrate. We, however, found that TiO(2) nanoparticles prepared via the sol-gel and hydrothermal synthetic routes each possess a definite specificity to the charge of the substrate for photodegradation. The nanoparticles were characterized by SEM, FTIR, XRD, TGA, and UV-visible spectra, and the photocatalytic degradation under UV-B (285 nm) irradiation of two model compounds, anionic methyl Orange (MO) and cationic methylene blue (MB) was monitored by a UV-visible spectrophotometer. Untreated sol-gel TiO(2) nanoparticles (T(sg)) preferentially degraded MO over MB (90% versus 40% in two hours), while after calcination at 400 °C for two hours (T(sgc)) they showed reversed specificity (50% MO versus 90% MB in one hour). The as-prepared hydrothermal TiO(2) nanoparticles (T(ht)) behaved in the opposite sense of T(sg) (41% MO versus 91% MB degraded in one and a half hours); calcination at 400 °C (T(htc)) did not reverse the trend but enhanced the efficiency of degradation. The study indicates that TiO(2) nanoparticles can be made to degrade a specific class of organic pollutants from an effluent facilitating the recycling of a specific class of pollutants for cost-effective effluent management. MDPI 2023-09-27 /pmc/articles/PMC10574600/ /pubmed/37836678 http://dx.doi.org/10.3390/molecules28196834 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Islam, Md. Torikul
Roni, Md. Nahid Parvez
Ali, Md. Yunus
Islam, Md. Robiul
Hossan, Md. Shamim
Rahman, M. Habibur
Zahid, A. A. S. Mostofa
Alam, Md. Nur E
Hanif, Md. Abu
Akhtar, M. Shaheer
Selectivity of Sol-Gel and Hydrothermal TiO(2) Nanoparticles towards Photocatalytic Degradation of Cationic and Anionic Dyes
title Selectivity of Sol-Gel and Hydrothermal TiO(2) Nanoparticles towards Photocatalytic Degradation of Cationic and Anionic Dyes
title_full Selectivity of Sol-Gel and Hydrothermal TiO(2) Nanoparticles towards Photocatalytic Degradation of Cationic and Anionic Dyes
title_fullStr Selectivity of Sol-Gel and Hydrothermal TiO(2) Nanoparticles towards Photocatalytic Degradation of Cationic and Anionic Dyes
title_full_unstemmed Selectivity of Sol-Gel and Hydrothermal TiO(2) Nanoparticles towards Photocatalytic Degradation of Cationic and Anionic Dyes
title_short Selectivity of Sol-Gel and Hydrothermal TiO(2) Nanoparticles towards Photocatalytic Degradation of Cationic and Anionic Dyes
title_sort selectivity of sol-gel and hydrothermal tio(2) nanoparticles towards photocatalytic degradation of cationic and anionic dyes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574600/
https://www.ncbi.nlm.nih.gov/pubmed/37836678
http://dx.doi.org/10.3390/molecules28196834
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