Development of HPLC/ESI-MS and HPLC/1H NMR methods for the identification of photocatalytic degradation products of iodosulfuron

被引:14
作者
Sleiman, Mohamad
Ferronato, Corinne
Fenet, Bernard
Baudot, Robert
Jaber, Farouk
Chovelon, Jean-Marc
机构
[1] Univ Lyon 1, UMR 5634, Lab Applicat Chim Environm, F-69622 Villeurbanne, France
[2] Univ Lyon 1, Ctr Commun RMN, CPE, F-69622 Villeurbanne, France
[3] CNRS, USR 059, Serv Cent Anal, Echangeur Solaize, F-69390 Vernaison, France
[4] Commiss Libanaise Energie Atom, Lab Pesticides & Micropollunts Organ, Beirut 11072260, Lebanon
关键词
D O I
10.1021/ac051836t
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the present study, HPLC/ESI-MS and stopped-flow HPLC/H-1 NMR methods were developed and applied to separate and characterize the byproducts arising from TiO2-catalyzed photodegradation of the herbicide iodosulfuron methyl ester (IOME) in aqueous solution under UV irradiation. Prior to identification, irradiated solutions of IOME (200 and 1000 mg.L-1) were concentrated by solid-phase extraction using two cartridges: Isolute C-18. and Isolute ENV+. Analytical separation was achieved on a C18 reversed-phase column with ACN/H2O (HPLC/MS) or ACN/D2O (HPLC/NMR) as mobile phase and a linear gradient with a chromatographic run time of 35 min. The combination of UV and MS data allowed the structural elucidation of more than 20 degradation products, whereas H-1 NMR data permitted an unequivocal confirmation of the identities of major products and the differentiation of several positional isomers, in particular, the hydroxylation isomers. The obtained results permitted us to propose a possible degradation scheme and to put in evidence the presence of privileged sites for the attack of OH radicals. This work shows, for the first time, the application of combined HPLC with UV, MS, and NMR detection for complete structural elucidation of photocatalytic degradation products, and it will be of particular value in studies on the elimination of pollutants in aqueous solutions by photocatalysis.
引用
收藏
页码:2957 / 2966
页数:10
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