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Photocatalytic degradation of 4-chlorophenol by UV/H(2)O(2)/NiO process in aqueous solution
The removal of 4-chlorophenol from aqueous phase continues to be an important environmental issue. In this work, the photochemical oxidation of 4-chlorophenol in aqueous solutions in a batch reactor using ultraviolet irradiation, hydrogen peroxide and nickel oxide was studied. The efficiency of the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561057/ https://www.ncbi.nlm.nih.gov/pubmed/23369233 http://dx.doi.org/10.1186/1735-2746-9-12 |
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author | Alimoradzadeh, Roya Assadi, Ali Nasseri, Simin Mehrasbi, Mohammad Reza |
author_facet | Alimoradzadeh, Roya Assadi, Ali Nasseri, Simin Mehrasbi, Mohammad Reza |
author_sort | Alimoradzadeh, Roya |
collection | PubMed |
description | The removal of 4-chlorophenol from aqueous phase continues to be an important environmental issue. In this work, the photochemical oxidation of 4-chlorophenol in aqueous solutions in a batch reactor using ultraviolet irradiation, hydrogen peroxide and nickel oxide was studied. The efficiency of the system was evaluated with respect to reaction time, pH, feed concentration of reactants, catalyst load, light intensity, and the reaction rate constant. The concentrations of 4-chlorophenol and chloride ions were determined by high performance liquid chromatography and ion chromatography, respectively. Pure nanosized nickel oxide was characterized by X-ray diffraction and scanning electron microscopy. The results showed that the optimum conditions (the complete 4-chlorophenol removal (100%) at 60 min) were obtained at a neutral pH, with 0.2 mol/L H(2)O(2), and 0.05 g/L of nickel oxide. However, no pH effects were observed in the range of 4–10. Analytical profiles on 4-chlorophenol transformation were consistent with the best line fit of the first-order kinetics. Moreover, the degradation rate constant increased with both UV light intensity and decreasing initial concentration of 4-chlorophenol. Finally, the results of mineralization and chloride ions studies indicated that dechlorination was better accomplished but more time was required to completely mineralize 4-chlorophenol into water and carbon dioxide. |
format | Online Article Text |
id | pubmed-3561057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35610572013-02-05 Photocatalytic degradation of 4-chlorophenol by UV/H(2)O(2)/NiO process in aqueous solution Alimoradzadeh, Roya Assadi, Ali Nasseri, Simin Mehrasbi, Mohammad Reza Iranian J Environ Health Sci Eng Research Article The removal of 4-chlorophenol from aqueous phase continues to be an important environmental issue. In this work, the photochemical oxidation of 4-chlorophenol in aqueous solutions in a batch reactor using ultraviolet irradiation, hydrogen peroxide and nickel oxide was studied. The efficiency of the system was evaluated with respect to reaction time, pH, feed concentration of reactants, catalyst load, light intensity, and the reaction rate constant. The concentrations of 4-chlorophenol and chloride ions were determined by high performance liquid chromatography and ion chromatography, respectively. Pure nanosized nickel oxide was characterized by X-ray diffraction and scanning electron microscopy. The results showed that the optimum conditions (the complete 4-chlorophenol removal (100%) at 60 min) were obtained at a neutral pH, with 0.2 mol/L H(2)O(2), and 0.05 g/L of nickel oxide. However, no pH effects were observed in the range of 4–10. Analytical profiles on 4-chlorophenol transformation were consistent with the best line fit of the first-order kinetics. Moreover, the degradation rate constant increased with both UV light intensity and decreasing initial concentration of 4-chlorophenol. Finally, the results of mineralization and chloride ions studies indicated that dechlorination was better accomplished but more time was required to completely mineralize 4-chlorophenol into water and carbon dioxide. BioMed Central 2012-11-27 /pmc/articles/PMC3561057/ /pubmed/23369233 http://dx.doi.org/10.1186/1735-2746-9-12 Text en Copyright ©2012 Alimoradzadeh et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Alimoradzadeh, Roya Assadi, Ali Nasseri, Simin Mehrasbi, Mohammad Reza Photocatalytic degradation of 4-chlorophenol by UV/H(2)O(2)/NiO process in aqueous solution |
title | Photocatalytic degradation of 4-chlorophenol by UV/H(2)O(2)/NiO process in aqueous solution |
title_full | Photocatalytic degradation of 4-chlorophenol by UV/H(2)O(2)/NiO process in aqueous solution |
title_fullStr | Photocatalytic degradation of 4-chlorophenol by UV/H(2)O(2)/NiO process in aqueous solution |
title_full_unstemmed | Photocatalytic degradation of 4-chlorophenol by UV/H(2)O(2)/NiO process in aqueous solution |
title_short | Photocatalytic degradation of 4-chlorophenol by UV/H(2)O(2)/NiO process in aqueous solution |
title_sort | photocatalytic degradation of 4-chlorophenol by uv/h(2)o(2)/nio process in aqueous solution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561057/ https://www.ncbi.nlm.nih.gov/pubmed/23369233 http://dx.doi.org/10.1186/1735-2746-9-12 |
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