کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6328742 1619775 2014 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Identification of Prometon, Deisopropylprometon, and Hydroxyprometon in Groundwater by High Resolution Liquid Chromatography/Mass Spectrometry
ترجمه فارسی عنوان
شناسایی پرومتون، دییزوپروپیلپروموتون و هیدروکسیپروموتون در آبهای زیرزمینی با استفاده از کروماتوگرافی مایع / اسپکترومتری مایع
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست شیمی زیست محیطی
چکیده انگلیسی
Prometon, a major soil sterilant, and its main transformation products, deisopropylprometon (N2-isopropyl-6-methoxy-1,3,5-triazine-2,4-diamine) and hydroxyprometon (4,6-bis(isopropylamino)-1,3,5-triazin-2-ol), were identified as the dominant triazine herbicides in groundwater samples from 51 locations in Colorado, USA, over a two-year time period. They were concentrated from water by solid phase extraction and detected using an ultrahigh pressure, liquid chromatography-quadrupole time of flight tandem mass spectrometry (UHPLC/QTOF-MS). The transformation products, deisopropylprometon and hydroxyprometon, were confirmed using MS-MS experiments. An original strategy was applied to form the degradation standards for deisopropylprometon and hydroxyprometon, which consisted of photo-degradation of prometon followed by MS-MS analysis. The concentration of prometon ranged from the detection limit of 3 ng · L- 1 to 87 ng · L- 1, hydroxyprometon ranged up to 50 ng · L- 1, and deisopropylprometon up to 100 ng · L- 1, with a frequency of detection of 80%, which was greater than the other triazines detected in the groundwater samples. A new ratio is proposed for prometon degradation called the “deisopropylprometon to prometon ratio” or the DIP ratio, as an indicator of prometon residence time in groundwater. Furthermore, these data suggest that prometon is more of an issue for groundwater contamination in urban areas rather than agricultural areas.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Science of The Total Environment - Volumes 497–498, 1 November 2014, Pages 459-466
نویسندگان
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