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Degradation of 4-Chlorophenol in Aqueous Solution by Sono-Electro-Fenton Process

Electro-Fenton (EF) and ultrasound radiation (US) have been of interest for the removal of chlorinated compounds from water. This study evaluates the effects of different parameters on sono-electro-Fenton (SEF) for degradation of 4-chlorophenol (4-CP) in an aqueous solution. This study uses pulsing...

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Autores principales: Nazari, Roya, Rajić, Ljiljana, Xue, Yunfei, Zhou, Wei, Alshawabkeh, Akram N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296483/
https://www.ncbi.nlm.nih.gov/pubmed/30568538
http://dx.doi.org/10.20964/2018.09.46
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author Nazari, Roya
Rajić, Ljiljana
Xue, Yunfei
Zhou, Wei
Alshawabkeh, Akram N.
author_facet Nazari, Roya
Rajić, Ljiljana
Xue, Yunfei
Zhou, Wei
Alshawabkeh, Akram N.
author_sort Nazari, Roya
collection PubMed
description Electro-Fenton (EF) and ultrasound radiation (US) have been of interest for the removal of chlorinated compounds from water. This study evaluates the effects of different parameters on sono-electro-Fenton (SEF) for degradation of 4-chlorophenol (4-CP) in an aqueous solution. This study uses pulsing US waves along with Pd-catalyzed EF to degrade contaminants in water while maintaining temperature. The usage of pulsing US waves along with Pd catalyzed EF to remove contaminants while maintaining temperature has not been reported previously. SEF ability to degrade 4-CP was compared with the performance of each process (EF and sonolysis) alone. Initial pH, current density, background electrolyte, Fe(2+) concentration, Pd/Al(2)O(3) catalyst concentration, US waves, and sonifier amplitude were optimized in a two electrode (Ti/mixed metal oxide or Ti/MMO) batch system. The degradation of 4-CP increased from 1.85% by US to 83% by EF to nearly >99.9% by coupled SEF. With US radiation under 70% amplitude and 1:10 ON/OFF ratio, the removal rate of 4-CP increased to 98% compared to 62% under EF alone within the first 120 min in the presence of 80 mg L(−1) Fe(2+), 16.94 mA cm(−2) of current density, 1 g L(−1) Pd/Al(2)O(3) catalyst (10 mg Pd), and initial pH of 3. However, the degradation rate decreased after 120 min of treatment, and complete 4-CP removal was observed after 300 minutes. The sonolysis impacted the 4-CP removal under coupled SEF, mostly due to the contribution of mass transfer (micromixing), while radical formation was found to be absent under the conditions tested (20kHz). The pulsed US was found to increase the temperature by only 8.7°C, which was found not to impact the 4-CP volatilization or degradation. These results imply that low-level US frequency through pulses is a practical and efficient approach to support electro-Fenton reaction, improving reaction rates without the need for electrolyte cooling.
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spelling pubmed-62964832018-12-17 Degradation of 4-Chlorophenol in Aqueous Solution by Sono-Electro-Fenton Process Nazari, Roya Rajić, Ljiljana Xue, Yunfei Zhou, Wei Alshawabkeh, Akram N. Int J Electrochem Sci Article Electro-Fenton (EF) and ultrasound radiation (US) have been of interest for the removal of chlorinated compounds from water. This study evaluates the effects of different parameters on sono-electro-Fenton (SEF) for degradation of 4-chlorophenol (4-CP) in an aqueous solution. This study uses pulsing US waves along with Pd-catalyzed EF to degrade contaminants in water while maintaining temperature. The usage of pulsing US waves along with Pd catalyzed EF to remove contaminants while maintaining temperature has not been reported previously. SEF ability to degrade 4-CP was compared with the performance of each process (EF and sonolysis) alone. Initial pH, current density, background electrolyte, Fe(2+) concentration, Pd/Al(2)O(3) catalyst concentration, US waves, and sonifier amplitude were optimized in a two electrode (Ti/mixed metal oxide or Ti/MMO) batch system. The degradation of 4-CP increased from 1.85% by US to 83% by EF to nearly >99.9% by coupled SEF. With US radiation under 70% amplitude and 1:10 ON/OFF ratio, the removal rate of 4-CP increased to 98% compared to 62% under EF alone within the first 120 min in the presence of 80 mg L(−1) Fe(2+), 16.94 mA cm(−2) of current density, 1 g L(−1) Pd/Al(2)O(3) catalyst (10 mg Pd), and initial pH of 3. However, the degradation rate decreased after 120 min of treatment, and complete 4-CP removal was observed after 300 minutes. The sonolysis impacted the 4-CP removal under coupled SEF, mostly due to the contribution of mass transfer (micromixing), while radical formation was found to be absent under the conditions tested (20kHz). The pulsed US was found to increase the temperature by only 8.7°C, which was found not to impact the 4-CP volatilization or degradation. These results imply that low-level US frequency through pulses is a practical and efficient approach to support electro-Fenton reaction, improving reaction rates without the need for electrolyte cooling. 2018-08-05 2018-09 /pmc/articles/PMC6296483/ /pubmed/30568538 http://dx.doi.org/10.20964/2018.09.46 Text en http://creativecommons.org/licenses/by/4.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license.
spellingShingle Article
Nazari, Roya
Rajić, Ljiljana
Xue, Yunfei
Zhou, Wei
Alshawabkeh, Akram N.
Degradation of 4-Chlorophenol in Aqueous Solution by Sono-Electro-Fenton Process
title Degradation of 4-Chlorophenol in Aqueous Solution by Sono-Electro-Fenton Process
title_full Degradation of 4-Chlorophenol in Aqueous Solution by Sono-Electro-Fenton Process
title_fullStr Degradation of 4-Chlorophenol in Aqueous Solution by Sono-Electro-Fenton Process
title_full_unstemmed Degradation of 4-Chlorophenol in Aqueous Solution by Sono-Electro-Fenton Process
title_short Degradation of 4-Chlorophenol in Aqueous Solution by Sono-Electro-Fenton Process
title_sort degradation of 4-chlorophenol in aqueous solution by sono-electro-fenton process
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296483/
https://www.ncbi.nlm.nih.gov/pubmed/30568538
http://dx.doi.org/10.20964/2018.09.46
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