首页> 美国卫生研究院文献>Springer Open Choice >Optimization and Simultaneous Determination of Alkyl Phenol Ethoxylates and Brominated Flame Retardants in Water after SPE and Heptafluorobutyric Anhydride Derivatization followed by GC/MS
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Optimization and Simultaneous Determination of Alkyl Phenol Ethoxylates and Brominated Flame Retardants in Water after SPE and Heptafluorobutyric Anhydride Derivatization followed by GC/MS

机译:固相萃取和七氟丁酸酐酐衍生化并进行GC / MS分析后同时测定水中的烷基苯酚乙氧基化物和溴代阻燃剂的优化与同时测定

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摘要

A gas chromatography–mass spectrometry (GC–MS) method was investigated for the simultaneous analysis of two types of endocrine disrupting compounds (EDCs), i.e., alkylphenol ethoxylates and brominated flame retardants (BFRs), by extraction and derivatization followed by GC–MS. Different solid phase extraction (SPE) cartridges (Cleanert PestiCarb, C18, Cleanert-SAX and Florosil), solvents (toluene, tetrahydrofuran, acetone, acetonitrile and ethyl acetate) and bases (NaHCO3, triethylamine and pyridine) were tested and the best chromatographic analysis was achieved by extraction with Strata-X (33 μm, Reverse Phase) cartridge and derivatization with heptafluorobutyric anhydride at 55 °C under Na2CO3 base in hexane. It was observed that APE together with lower substituted PBBs (PBB1, PBB10, PBB18 and PBB49), HBCD and TBBPA can be determined simultaneously under the same GC conditions. This simple and reliable analytical method was applied to determining trace amounts of these compounds from wastewater treatment plant samples. The recoveries of the target compounds from simulated water were above 60 %. The limit of detection ranged from 0.01 to 0.15 μg L−1 and the limit of quantification ranged from 0.05 to 0.66 μg L−1. There were no appreciable differences between filtered and unfiltered wastewater samples from Leeuwkil treatment plant although concentration of target analytes in filtered influent was slightly lower than the concentration of target analytes in unfiltered influent water. The concentrations of the target compounds from the wastewater treatment were determined from LOQ upwards.
机译:研究了气相色谱-质谱(GC-MS)方法,通过萃取和衍生化同时分析两种类型的内分泌干扰化合物(EDC),即烷基酚乙氧基化物和溴化阻燃剂(BFR)。 。测试了不同的固相萃取(SPE)柱(Cleanert PestiCarb,C18,Cleanert-SAX和Florosil),溶剂(甲苯,四氢呋喃,丙酮,乙腈和乙酸乙酯)和碱(NaHCO3,三乙胺和吡啶)并进行了最佳色谱分析通过用Strata-X(33μm,反相)柱萃取,并在己烷中Na2CO3碱下于55°C在55°C下用七氟丁酸酐衍生化来实现。据观察,可以在相同的GC条件下同时测定APE以及较低取代的PBB(PBB1,PBB10,PBB18和PBB49),HBCD和TBBPA。这种简单而可靠的分析方法可用于测定废水处理厂样品中的痕量这些化合物。从模拟水中回收的目标化合物的回收率高于60%。检测限范围为0.01至0.15μgL -1 ,定量限范围为0.05至0.66μgL -1 。尽管在过滤后的进水中目标分析物的浓度略低于未过滤进水中目标分析物的浓度,但来自吕伐基尔污水处理厂的过滤后和未过滤废水样品之间没有明显差异。从LOQ开始确定废水处理中目标化合物的浓度。

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