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Acid green crystal-based in situ synthesis of polyaniline hollow nanotubes for the adsorption of anionic and cationic dyes

In this article, acid green (AG) dye played a dual pivotal role. The first role is as a structure-guiding agent and a soft template for the acid-free synthesis of polyaniline hollow nanotubes (PANI-HNTs) while the second role is as a target dye to be removed as a model of anionic dyes, alongside met...

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Autores principales: Amer, Wael A., Omran, Mohamed M., Rehab, Ahmed F., Ayad, Mohamad M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081471/
https://www.ncbi.nlm.nih.gov/pubmed/35539738
http://dx.doi.org/10.1039/c8ra02236d
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author Amer, Wael A.
Omran, Mohamed M.
Rehab, Ahmed F.
Ayad, Mohamad M.
author_facet Amer, Wael A.
Omran, Mohamed M.
Rehab, Ahmed F.
Ayad, Mohamad M.
author_sort Amer, Wael A.
collection PubMed
description In this article, acid green (AG) dye played a dual pivotal role. The first role is as a structure-guiding agent and a soft template for the acid-free synthesis of polyaniline hollow nanotubes (PANI-HNTs) while the second role is as a target dye to be removed as a model of anionic dyes, alongside methylene blue (MB) as a model of cationic dyes. After characterization using X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy (TEM), nitrogen adsorption–desorption isotherms (BET), and UV-visible absorption spectroscopy techniques, the prepared PANI-HNTs were exploited for the adsorption of basic MB dye and acidic AG dye from aqueous media. To optimize the adsorption process, the effects of different variables, such as adsorbent dose, contact time and pH, were studied. Due to the structural differences between the MB and AG dyes, the obtained data revealed that the best pH for the medium for optimal adsorption was 9.0 and 3.0, respectively. The rapid sorption dynamics were found to proceed in a second-order kinetic model and the equilibrium data for the adsorption of MB and AG dyes were fitted well to the Langmuir isotherm. The maximum monolayer capacity, q(max), for MB and AG was calculated from the Langmuir model and equalled 69.4 and 57.8 mg g(−1), respectively. A thermodynamic study revealed that the adsorption of MB by PANI-HNTs was a feasible, spontaneous, and exothermic process. Investigation of the substrate regeneration revealed that PANI-HNTs can be reused for dye adsorption several times. Therefore, the synthesized PANI-NTs are highly efficient for the dual removal of basic and acidic dyes. TEM images showed that PANI-HNTs were formed with an external and internal diameter of 50–60 nm and 5–10 nm, respectively.
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spelling pubmed-90814712022-05-09 Acid green crystal-based in situ synthesis of polyaniline hollow nanotubes for the adsorption of anionic and cationic dyes Amer, Wael A. Omran, Mohamed M. Rehab, Ahmed F. Ayad, Mohamad M. RSC Adv Chemistry In this article, acid green (AG) dye played a dual pivotal role. The first role is as a structure-guiding agent and a soft template for the acid-free synthesis of polyaniline hollow nanotubes (PANI-HNTs) while the second role is as a target dye to be removed as a model of anionic dyes, alongside methylene blue (MB) as a model of cationic dyes. After characterization using X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy (TEM), nitrogen adsorption–desorption isotherms (BET), and UV-visible absorption spectroscopy techniques, the prepared PANI-HNTs were exploited for the adsorption of basic MB dye and acidic AG dye from aqueous media. To optimize the adsorption process, the effects of different variables, such as adsorbent dose, contact time and pH, were studied. Due to the structural differences between the MB and AG dyes, the obtained data revealed that the best pH for the medium for optimal adsorption was 9.0 and 3.0, respectively. The rapid sorption dynamics were found to proceed in a second-order kinetic model and the equilibrium data for the adsorption of MB and AG dyes were fitted well to the Langmuir isotherm. The maximum monolayer capacity, q(max), for MB and AG was calculated from the Langmuir model and equalled 69.4 and 57.8 mg g(−1), respectively. A thermodynamic study revealed that the adsorption of MB by PANI-HNTs was a feasible, spontaneous, and exothermic process. Investigation of the substrate regeneration revealed that PANI-HNTs can be reused for dye adsorption several times. Therefore, the synthesized PANI-NTs are highly efficient for the dual removal of basic and acidic dyes. TEM images showed that PANI-HNTs were formed with an external and internal diameter of 50–60 nm and 5–10 nm, respectively. The Royal Society of Chemistry 2018-06-20 /pmc/articles/PMC9081471/ /pubmed/35539738 http://dx.doi.org/10.1039/c8ra02236d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Amer, Wael A.
Omran, Mohamed M.
Rehab, Ahmed F.
Ayad, Mohamad M.
Acid green crystal-based in situ synthesis of polyaniline hollow nanotubes for the adsorption of anionic and cationic dyes
title Acid green crystal-based in situ synthesis of polyaniline hollow nanotubes for the adsorption of anionic and cationic dyes
title_full Acid green crystal-based in situ synthesis of polyaniline hollow nanotubes for the adsorption of anionic and cationic dyes
title_fullStr Acid green crystal-based in situ synthesis of polyaniline hollow nanotubes for the adsorption of anionic and cationic dyes
title_full_unstemmed Acid green crystal-based in situ synthesis of polyaniline hollow nanotubes for the adsorption of anionic and cationic dyes
title_short Acid green crystal-based in situ synthesis of polyaniline hollow nanotubes for the adsorption of anionic and cationic dyes
title_sort acid green crystal-based in situ synthesis of polyaniline hollow nanotubes for the adsorption of anionic and cationic dyes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081471/
https://www.ncbi.nlm.nih.gov/pubmed/35539738
http://dx.doi.org/10.1039/c8ra02236d
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