Photodegradation of several triazidic and organophosphorus pesticides in water by pulsed light technology

被引:27
作者
Beatriz Baranda, Ana [1 ]
Fundazuri, Olatz [2 ]
Martinez de Maranon, Inigo [1 ]
机构
[1] AZTI Tecnalia, Food Res Div, Derio 48160, Bizkaia, Spain
[2] BIOFUNGITEK SL, Derio 48170, Bizkaia, Spain
关键词
Pesticide; Decontamination; Water; UV; Pulsed light; Photoproducts; ADVANCED OXIDATION PROCESSES; AQUEOUS-SOLUTIONS; AZINPHOS-METHYL; UV; ATRAZINE; DEGRADATION; PHOTOCHEMISTRY; DISINFECTION; PHOTOLYSIS; OZONATION;
D O I
10.1016/j.jphotochem.2014.03.015
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Pulsed light technology consists of a successive repetition of short duration (325 mu s) and high power flashes emitted by xenon lamps. These flashlamps radiate a broadband emission light (approximately 200-1000 nm) with a considerable amount of light in the short-wave UV spectrum. In the present work, this technology was tested as a new tool for the degradation of several herbicides in water: simazine, atrazine, phosmet, azinphos-methyl, methyl-parathion, pirimiphos-methyl and chlorpyrifos-ethyl. To evaluate the presence and evolution with time of these herbicides, as well as the formation of derivatives, liquid chromatography mass spectrometry (atmospheric pressure chemical ionization) ion trap operating in positive mode was used. The degradation process followed first-order kinetics for all studied compounds except for parathion. Fluences about 4.65 J/cm(2) induced 50% reduction of simazine, atrazine, phosmet, azinphos-ethyl and pirimiphos-ethyl, independently of these compounds were PL treated separately or mixed in an aqueous solution. A higher fluence (9.81 J/cm(2)) was needed to induce 50% reduction for chlorpyrifos-ethyl, being more difficult to degrade it in presence of other pesticides in the same solution. While simazine and atrazine were degraded, no chlorinated photoproducts were formed. Partial dechlorination was also observed for chlorpyrifos-ethyl. For the rest of organophosphorus pesticides different kinds of reactions could be suggested such as oxidative desulfuration, oxidation of ethyl groups or N-dealkylations. The molecular structures for some of derivatives could be proposed. The different formation profiles of photoproducts suggested that the degradation pathway may include several successive and competitive steps, with subsequent degradation processes taking part from the already formed degradation products. According to the degradation efficiency, the short treatment time and the type of derivatives, this new technology could be considered as an alternative for water treatment. (C) 2014 Published by Elsevier B.V.
引用
收藏
页码:29 / 39
页数:11
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