首页> 外文期刊>Analytical Chemistry >SIMULTANEOUS DETERMINATION OF TRIAZINES INCLUDING ATRAZINE AND THEIR MAJOR METABOLITES HYDROXYATRAZINE, DESETHYLATRAZINE, AND DEISOPROPYLATRAZINE IN NATURAL WATERS
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SIMULTANEOUS DETERMINATION OF TRIAZINES INCLUDING ATRAZINE AND THEIR MAJOR METABOLITES HYDROXYATRAZINE, DESETHYLATRAZINE, AND DEISOPROPYLATRAZINE IN NATURAL WATERS

机译:同时测定天然水中的三嗪类药物(包括阿特拉津及其主要代谢物)羟嗪,去甲乙嗪和去甲丙嗪

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This paper describes the simultaneous quantification of the herbicides atrazine (AT), simazine (SIM), terbutylazine (TER), propazine (PROP), and prometryne (FROM) and their major metabolites hydroxyatrazine (ATOH), hydroxypropazine (PROH), desethylatrazine (DEA), and deisopropylatrazine (DIA) in natural waters at the low nanograms per liter concentration level (3-1500 ng/L). These herbicides and their metabolites were determined in surface water, groundwater, rainwater, roof runoff, and wastewater, The compounds were enriched on graphitized carbon black (GCB) and analyzed with reversed-phase high-performance liquid chromatography (HPLC) using a diode array UV detector (DAD). The recoveries for hydroxyatrazine and hydroxypropazine from spiked Nanopure water were 93 +/- 6.9% and 92 +/- 7.0%, respectively, For all other compounds, the recovery ranged between 97 +/- 4.8% and 101 +/- 3.3% in Nanopure water (fortified with 50-900 ng/L) and between 88 +/- 9.0% and 108 +/- 13% in lake water (spiked with 50-150 ng/L), respectively, The detection limits were 2-7 ng/L in pure water and 3-11 ng/L in environmental samples, The mean relative standard deviation (RSD) was 6.2% (ranging from 0.9% to 15%) in natural waters. The method was compared to gas chromatography/mass spectrometry (GC/MS) techniques using deuterioatrazine as an internal standard. Both methods produced consistent results for the parent compounds, while the HPLC method was more precise for the determination of the metabolite concentrations. The HPLC method described allows for the first time the routine quantification of very low concentrations (<20 ng/L) of hydroxyatrazine together with other triazines in a single analytical procedure.
机译:本文介绍了同时定量除草剂阿特拉津(AT),西玛津(SIM),叔丁嗪(TER),丙嗪(PROP)和pro啶酮(FROM)及其主要代谢物的方法DEA)和天然水中的去异丙基at去津(DIA),浓度低至纳克每升(3-1500 ng / L)。在地表水,地下水,雨水,屋顶径流和废水中测定了这些除草剂及其代谢物,并在石墨化炭黑(GCB)上富集了这些化合物,并使用二极管阵列通过反相高效液相色谱(HPLC)进行了分析。紫外线检测器(DAD)。从加标的纳米级纯水中,羟基阿特拉津和羟基丙嗪的回收率分别为93 +/- 6.9%和92 +/- 7.0%。对于所有其他化合物,回收率在97 +/- 4.8%和101 +/- 3.3%之间。纳米纯水(强化浓度为50-900 ng / L)和湖水(浓度为50-150 ng / L)分别介于88 +/- 9.0%和108 +/- 13%之间,检出限为2-7纯水中的ng / L和环境样品中的3-11 ng / L,天然水的平均相对标准偏差(RSD)为6.2%(范围从0.9%到15%)。该方法与使用氘化阿特拉津为内标的气相色谱/质谱(GC / MS)技术进行了比较。两种方法均对母体化合物产生一致的结果,而HPLC方法更精确地确定了代谢物的浓度。所描述的HPLC方法首次允许在单个分析程序中对非常低浓度(<20 ng / L)的羟at去津和其他三嗪进行常规定量。

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