Peñuela G A, Barceló D
Instituto de Investigaciones Quimicas y Ambientales de Barcelona-Consejo Superior de Investigaciones Cientificas (IIQAB-CSIC), Department of Environmental Chemistry, Spain.
J AOAC Int. 2000 Jan-Feb;83(1):53-60.
Results are reported for a comparative photodegradation study of atrazine and desethylatrazine in water using TiO2/H2O2, FeCl3/H2O2, and photolysis. Deionized water and ground water spiked with atrazine or desethylatrazine at 36 micrograms/L were irradiated by using a xenon arc lamp and/or sunlight. After irradiation, the water samples containing the spiked pesticides were preconcentrated by using C18 solid-phase extraction disks and analyzed by gas chromatography with nitrogen-phosphorus and mass spectrometric detection. A relative percentage of 7% desethylatrazine was detected in samples removed after 20 and 4 min of sensitized photodegradation with TiO2 and Fe3+, respectively. Atrazine and desethylatrazine did not degrade when solar irradiation (in winter) and deionized water were used. Atrazine degraded faster than desethylatrazine when a xenon arc lamp or sunlight plus FeCl3 was used, with half-lives varying from 5 to 11 min and from 19 to 26 min, respectively. In other photodegradation experiments, the degradation of atrazine was slightly higher than that of desethylatrazine. This study shows that desethylatrazine has slightly higher stability than atrazine in environmental water samples; this stability accounts for the frequent detection of desethylatrazine together with atrazine in natural waters.
本文报道了使用TiO2/H2O2、FeCl3/H2O2和光解作用对水中莠去津和去乙基莠去津进行的对比光降解研究结果。用氙弧灯和/或阳光照射添加了浓度为36微克/升莠去津或去乙基莠去津的去离子水和地下水。辐照后,使用C18固相萃取盘对含有添加农药的水样进行预浓缩,并通过带有氮磷检测器和质谱检测器的气相色谱法进行分析。在用TiO2和Fe3+进行敏化光降解20分钟和4分钟后取出的样品中,分别检测到相对比例为7%的去乙基莠去津。当使用太阳辐射(冬季)和去离子水时,莠去津和去乙基莠去津不会降解。当使用氙弧灯或阳光加FeCl3时,莠去津的降解速度比去乙基莠去津快,半衰期分别为5至11分钟和19至26分钟。在其他光降解实验中,莠去津的降解略高于去乙基莠去津。本研究表明,在环境水样中,去乙基莠去津的稳定性略高于莠去津;这种稳定性解释了在天然水中经常同时检测到去乙基莠去津和莠去津的原因。