Formation of the intermediates and by-products during the degradation of diclofenac by ozonation

碩士 === 國立臺灣大學 === 環境工程學研究所 === 99 === Diclofenac (DFC) is a widely used anti-inflammatory drug and thus enters the aquatic environment. The realistic environmental concentration levels at harmful effects to different organisms have been demonstrated by many previous studies. Many investigations ha...

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Main Authors: Nai-Hsin Hu, 胡乃心
Other Authors: Pen-Chi Chiang
Format: Others
Language:en_US
Published: 2011
Online Access:http://ndltd.ncl.edu.tw/handle/77460412898955612827
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spelling ndltd-TW-099NTU055150252015-10-16T04:03:07Z http://ndltd.ncl.edu.tw/handle/77460412898955612827 Formation of the intermediates and by-products during the degradation of diclofenac by ozonation 臭氧去除Diclofenac及其中間產物、副產物生成之研究 Nai-Hsin Hu 胡乃心 碩士 國立臺灣大學 環境工程學研究所 99 Diclofenac (DFC) is a widely used anti-inflammatory drug and thus enters the aquatic environment. The realistic environmental concentration levels at harmful effects to different organisms have been demonstrated by many previous studies. Many investigations have revealed that diclofenac can not be completely removed by conventional sewage treatment plants (STP) and was detected in STP effluents at trace levels. Therefore, the presence of diclofenac in the aquatic environment should be assessed critically. The objective of this study was to evaluate the removal of diclofenac using ozonation process. The effect of various operating parameters including ozone dose, pH, and the presence of phosphate buffer on the removal of diclofenac and TOC in ozonation process was investigated. In addition, the formation of ozonation by-products, including chloride, ammonia ions, intermediates and aldehyde, was also studied. Meanwhile, a simplified mass balance based on intermediates containing carbon, chlorine, and nitrogen was developed to determine the formation rate constants of CO2, chloride, and ammonia. Furthermore, kinetic studies based on the degradation of diclofenac and formation of chloride and ammonia were also developed to determine the selectivity of reaction pathway and rate constants of diclofenac. Finally, the constants obtained in this study were used to propose the possible pathway and evaluate the optimum operational parameters. The results show that ozonation was efficient in degrading diclofenac. In absence of phosphate buffer, the removal of diclofenac and TOC, and formation rate of chloride basically increased as the ozone doses increased. In presence of phosphate buffer, the maximal diclofenac removal and CO2 formation rate constant is at pH 7.4 at two levels of ozone dose. The reaction rate constants of DFC can be determined in a second order reaction. The diclofenac degradation models can predict the selectivity of pathway. In addition, the aldehyde concentration increased with increasing pH in the ozonation process, which indicated the involvement of hydroxyl radical in aldehyde formation. Pen-Chi Chiang 蔣本基 2011 學位論文 ; thesis 127 en_US
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language en_US
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description 碩士 === 國立臺灣大學 === 環境工程學研究所 === 99 === Diclofenac (DFC) is a widely used anti-inflammatory drug and thus enters the aquatic environment. The realistic environmental concentration levels at harmful effects to different organisms have been demonstrated by many previous studies. Many investigations have revealed that diclofenac can not be completely removed by conventional sewage treatment plants (STP) and was detected in STP effluents at trace levels. Therefore, the presence of diclofenac in the aquatic environment should be assessed critically. The objective of this study was to evaluate the removal of diclofenac using ozonation process. The effect of various operating parameters including ozone dose, pH, and the presence of phosphate buffer on the removal of diclofenac and TOC in ozonation process was investigated. In addition, the formation of ozonation by-products, including chloride, ammonia ions, intermediates and aldehyde, was also studied. Meanwhile, a simplified mass balance based on intermediates containing carbon, chlorine, and nitrogen was developed to determine the formation rate constants of CO2, chloride, and ammonia. Furthermore, kinetic studies based on the degradation of diclofenac and formation of chloride and ammonia were also developed to determine the selectivity of reaction pathway and rate constants of diclofenac. Finally, the constants obtained in this study were used to propose the possible pathway and evaluate the optimum operational parameters. The results show that ozonation was efficient in degrading diclofenac. In absence of phosphate buffer, the removal of diclofenac and TOC, and formation rate of chloride basically increased as the ozone doses increased. In presence of phosphate buffer, the maximal diclofenac removal and CO2 formation rate constant is at pH 7.4 at two levels of ozone dose. The reaction rate constants of DFC can be determined in a second order reaction. The diclofenac degradation models can predict the selectivity of pathway. In addition, the aldehyde concentration increased with increasing pH in the ozonation process, which indicated the involvement of hydroxyl radical in aldehyde formation.
author2 Pen-Chi Chiang
author_facet Pen-Chi Chiang
Nai-Hsin Hu
胡乃心
author Nai-Hsin Hu
胡乃心
spellingShingle Nai-Hsin Hu
胡乃心
Formation of the intermediates and by-products during the degradation of diclofenac by ozonation
author_sort Nai-Hsin Hu
title Formation of the intermediates and by-products during the degradation of diclofenac by ozonation
title_short Formation of the intermediates and by-products during the degradation of diclofenac by ozonation
title_full Formation of the intermediates and by-products during the degradation of diclofenac by ozonation
title_fullStr Formation of the intermediates and by-products during the degradation of diclofenac by ozonation
title_full_unstemmed Formation of the intermediates and by-products during the degradation of diclofenac by ozonation
title_sort formation of the intermediates and by-products during the degradation of diclofenac by ozonation
publishDate 2011
url http://ndltd.ncl.edu.tw/handle/77460412898955612827
work_keys_str_mv AT naihsinhu formationoftheintermediatesandbyproductsduringthedegradationofdiclofenacbyozonation
AT húnǎixīn formationoftheintermediatesandbyproductsduringthedegradationofdiclofenacbyozonation
AT naihsinhu chòuyǎngqùchúdiclofenacjíqízhōngjiānchǎnwùfùchǎnwùshēngchéngzhīyánjiū
AT húnǎixīn chòuyǎngqùchúdiclofenacjíqízhōngjiānchǎnwùfùchǎnwùshēngchéngzhīyánjiū
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