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首页> 外文期刊>Analytical methods >Application of ultrasound-assisted dispersive liquid-liquid microextraction and automated in-port silylation for the simultaneous determination of phenolic endocrine disruptor chemicals in water samples by gas chromatography-triple quadrupole mass spectrometry
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Application of ultrasound-assisted dispersive liquid-liquid microextraction and automated in-port silylation for the simultaneous determination of phenolic endocrine disruptor chemicals in water samples by gas chromatography-triple quadrupole mass spectrometry

机译:超声辅助分散液-液微萃取和自动入口硅烷化技术在气相色谱-三重四极杆质谱法同时测定水样中酚类内分泌干扰物中的应用

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An analytical methodology has been developed based on ultrasound-assisted dispersive liquid-liquid microextraction (UA-DLLME) coupled to automated in-port silylation (auto-IPS) for the simultaneous determination of ten phenolic endocrine disruptor chemicals (PEDCs) which include alkylphenols, parabens and bisphenols. Optimization of DLLME parameters includes the type and volume of extraction and disperser solvent, pH, ionic strength and sonication time. Under the optimized conditions, acetone (200 ??L) and dichloromethane (100 ??L) were rapidly injected into 2 mL of water sample and sonicated for 90 s. After centrifugation the sedimented phase was taken into a gas chromatography-mass spectrometry autosampler vial and subjected to auto-IPS with bis(trimethylsilyl)trifluoroacetamide containing 1% trimethylchlorosilane (BSTFA + TMCS; 99:1 v/v). Auto-IPS parameters such as the effect of solvent, injector port temperature and the ratio of the volume of the sedimented phase to BSTFA were thoroughly studied. The PEDCs were analyzed by gas chromatography-tandem mass spectrometry in the selected reaction monitoring mode. Linearity in the range of 0.01a€“500 ??g La?’1 was obtained for all the PEDCs. The limit of detection and limit of quantification were found to be in the range of 0.002a€“0.23 ??g La?’1 and 0.009a€“0.77 ??g La?’1, respectively. Satisfactory recoveries ranging from 82a€“98% were achieved for all the PEDCs. In conclusion, the coupling of UA-DLLME with auto-IPS greatly reduces the amount of solvents used for extraction, costly reagent for derivatization and time of sample preparation plus derivatization, resulting in a rapid, sensitive, economical and eco-friendly method which could be of immense use in the routine analysis of water samples for regulatory purposes.
机译:已开发了一种基于超声辅助的分散液-液微萃取(UA-DLLME)与自动港口内甲硅烷基化(auto-IPS)结合的分析方法,用于同时测定包括烷基酚在内的十种酚类内分泌干扰物(PEDC),对羟基苯甲酸酯和双酚。 DLLME参数的优化包括萃取和分散剂溶剂的类型和体积,pH,离子强度和超声处理时间。在优化的条件下,将丙酮(200升)和二氯甲烷(100升)快速注入2 mL水样品中,并超声处理90 s。离心后,将沉淀相放入气相色谱-质谱自动进样器小瓶中,并与含有1%三甲基氯硅烷(BSTFA + TMCS; 99:1 v / v)的双(三甲基甲硅烷基)三氟乙酰胺进行自动IPS分离。彻底研究了自动IPS参数,例如溶剂的影响,进样器端口温度以及沉淀相与BSTFA的体积比。在选定的反应监测模式下,通过气相色谱-串联质谱法分析PEDC。对于所有PEDC,线性度都在0.01a?500?g La?1的范围内。发现的检出限和定量限分别在0.002a·“ 0.23 g·g La?’1和0.009a·0.77 g·g La?’1的范围内。所有PEDC的回收率均令人满意,在82%至98%之间。总之,UA-DLLME与auto-IPS的结合极大地减少了萃取所用的溶剂数量,昂贵的衍生试剂以及样品制备和衍生的时间,从而产生了一种快速,灵敏,经济且环保的方法,可以在用于监管目的的水样常规分析中有大量用途。

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