Photocatalytic Degradation of Trifluralin, Clodinafop-Propargyl, and 1,2-Dichloro-4-Nitrobenzene As Determined by Gas Chromatography Coupled with Mass Spectrometry
Phototransformation is considered one of the most key factors affecting the fate of pesticides. Therefore, our study focused on photocatalytic degradation of three selected pesticide derivatives: trifluralin (1), clodinafop-propargyl (2), and 1,2-dichloro-4-nitrobenzene (3). The degradation was carr...
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description | Phototransformation is considered one of the most key factors affecting the fate of pesticides. Therefore, our study focused on photocatalytic degradation of three selected pesticide derivatives: trifluralin (1), clodinafop-propargyl (2), and 1,2-dichloro-4-nitrobenzene (3). The degradation was carried out in acetonitrile/water medium in the presence of titanium dioxide (TiO2) under continuous purging of atmospheric air. The course of degradation was followed by thin-layer chromatography and gas chromatography-mass spectrometry techniques. Electron ionization mass spectrometry was used to identify the degradation species. GC-MS analysis indicates the formation of several intermediate products which have been characterized on the basis of molecular ion, mass fragmentation pattern, and comparison with NIST library. The photocatalytic degradation of pesticides of different chemical structures manifested distinctly different degradation mechanism. The major routes for the degradation of pesticides were found to be (a) dealkylation, dehalogenation, and decarboxylation, (b) hydroxylation, (c) oxidation of side chain, if present, (d) isomerization and cyclization, (e) cleavage of alkoxy bond, and (f) reduction of triple bond to double bond and nitro group to amino. |
doi_str_mv | 10.1155/2014/261683 |
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Therefore, our study focused on photocatalytic degradation of three selected pesticide derivatives: trifluralin (1), clodinafop-propargyl (2), and 1,2-dichloro-4-nitrobenzene (3). The degradation was carried out in acetonitrile/water medium in the presence of titanium dioxide (TiO2) under continuous purging of atmospheric air. The course of degradation was followed by thin-layer chromatography and gas chromatography-mass spectrometry techniques. Electron ionization mass spectrometry was used to identify the degradation species. GC-MS analysis indicates the formation of several intermediate products which have been characterized on the basis of molecular ion, mass fragmentation pattern, and comparison with NIST library. The photocatalytic degradation of pesticides of different chemical structures manifested distinctly different degradation mechanism. The major routes for the degradation of pesticides were found to be (a) dealkylation, dehalogenation, and decarboxylation, (b) hydroxylation, (c) oxidation of side chain, if present, (d) isomerization and cyclization, (e) cleavage of alkoxy bond, and (f) reduction of triple bond to double bond and nitro group to amino.</description><identifier>ISSN: 2090-3502</identifier><identifier>EISSN: 2090-3510</identifier><identifier>DOI: 10.1155/2014/261683</identifier><language>eng</language><publisher>New York: Hindawi Publishing Corporation</publisher><subject>Herbicides ; Mass spectrometry ; Pesticides ; Photocatalysis</subject><ispartof>Chromatography research international, 2014-12, Vol.2014, p.1-9</ispartof><rights>Copyright © 2014 Niyaz A. Mir et al.</rights><rights>Copyright © 2014 Niyaz A. Mir et al. Niyaz A. Mir et al. 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The major routes for the degradation of pesticides were found to be (a) dealkylation, dehalogenation, and decarboxylation, (b) hydroxylation, (c) oxidation of side chain, if present, (d) isomerization and cyclization, (e) cleavage of alkoxy bond, and (f) reduction of triple bond to double bond and nitro group to amino.</description><subject>Herbicides</subject><subject>Mass spectrometry</subject><subject>Pesticides</subject><subject>Photocatalysis</subject><issn>2090-3502</issn><issn>2090-3510</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kc1q3DAUhU1poEOSVV9A0F0yTvRnjb0cPElamCYDna7NtX5iBY_kShqC-zp90ShM6bJ3cy_cj3M4nKL4TPANIVV1SzHht1QQUbMPxYLiBpesIvjjvxvTT8VljC84T7VqmhVfFH92g09eQoJxTlaijX4OoCBZ75A3aB-sGY8BRuuWqB29sg6Mn8pd8BOE53lcInAKkSUtN1YOow--5OWjTcH32v3WTqN1zKJJh4N1WqF-Rg8QUTsEf4Dks9k0zKj1x2nM31ebBvQdYkQ_Ji2zyEGnMF8UZwbGqC__7vPi5_3dvv1abp8evrXrbQmUV6wUjACXIKgSvO-FWnGDNRhJDZE5u5I91MBNzzhmpFcrQmtqqKl6JhpR1w07L76cdKfgfx11TN2LPwaXLTtSCdKwuq6rTF2fKBl8jEGbbgr2AGHuCO7ei-jei-hORWT66kQP1il4tf-F3wBzNolS</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Mir, Niyaz A.</creator><creator>Khan, A.</creator><creator>Muneer, M.</creator><creator>Vijayalakhsmi, S.</creator><general>Hindawi Publishing Corporation</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20141201</creationdate><title>Photocatalytic Degradation of Trifluralin, Clodinafop-Propargyl, and 1,2-Dichloro-4-Nitrobenzene As Determined by Gas Chromatography Coupled with Mass Spectrometry</title><author>Mir, Niyaz A. ; 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Therefore, our study focused on photocatalytic degradation of three selected pesticide derivatives: trifluralin (1), clodinafop-propargyl (2), and 1,2-dichloro-4-nitrobenzene (3). The degradation was carried out in acetonitrile/water medium in the presence of titanium dioxide (TiO2) under continuous purging of atmospheric air. The course of degradation was followed by thin-layer chromatography and gas chromatography-mass spectrometry techniques. Electron ionization mass spectrometry was used to identify the degradation species. GC-MS analysis indicates the formation of several intermediate products which have been characterized on the basis of molecular ion, mass fragmentation pattern, and comparison with NIST library. The photocatalytic degradation of pesticides of different chemical structures manifested distinctly different degradation mechanism. 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subjects | Herbicides Mass spectrometry Pesticides Photocatalysis |
title | Photocatalytic Degradation of Trifluralin, Clodinafop-Propargyl, and 1,2-Dichloro-4-Nitrobenzene As Determined by Gas Chromatography Coupled with Mass Spectrometry |
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