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首页> 外文期刊>Analytical chemistry >Single-Step LC/MS Method for the Simultaneous Determination of GC-Amenable Organochlorine and LC-Amenable Phenoxy Acidic Pesticides
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Single-Step LC/MS Method for the Simultaneous Determination of GC-Amenable Organochlorine and LC-Amenable Phenoxy Acidic Pesticides

机译:一步LC / MS方法同时测定适合GC的有机氯和适合LC的苯氧基酸性农药

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摘要

Water pollution by organochlorine pesticides (OCPs) is considered as an analytical challenge, since these persistent and nonbiodegradable pollutants are not amenable by liquid chromatography coupled to atmospheric pressure ionization mass spectrometry (LC/API-MS). This represents a significant constraint in multiresidue analysis of real samples, when high polar, poorly volatile compounds are present as well. This paper reports the development of an innovative single-step method for the simultaneous determination of OCPs and polar pesticides belonging to the class of phenoxy acids in water samples. The method is based on an off-line solid-phase extraction (SPE) procedure with Carbograph 4 followed by liquid chromatography coupled to a direct electron ionization mass spectrometer (LC/direct-EI-MS). The direct-EI capability of acquiring high-quality EI spectra and operation in selected ion monitoring mode allowed a precise quantification of OCPs and phenoxy acids in a single chromatographic run without derivatization. The instrumental response was characterized by excellent sensitivity, linearity, and precision. The SPE recovery rates in river water gave values equal or better than 80percent for most of the compounds. The method limits of detection (LODs) span from 0.002 to 0.052 (mu)g/L, allowing the detection of the selected pesticides at the limits required by the European Union (EU) legislation for drinking water.
机译:有机氯农药(OCP)对水的污染被认为是分析挑战,因为这些持久性和不可生物降解的污染物无法通过液相色谱与大气压电离质谱联用(LC / API-MS)进行处理。当还存在高极性,难挥发的化合物时,这代表了对真实样品进行多残留分析的重要限制。本文报告了一种创新的单步方法的开发,该方法可以同时测定水样中的苯酚酸类中的OCP和极性农药。该方法基于使用Carbograph 4的离线固相萃取(SPE)程序,然后将液相色谱与直接电子电离质谱仪(LC / direct-EI-MS)耦合。直接EI能够获得高质量EI光谱并在选定的离子监测模式下运行,从而能够在不进行衍生化的情况下,在一次色谱操作中精确定量OCP和苯氧基酸。仪器响应具有出色的灵敏度,线性和精度。对于大多数化合物,在河水中的SPE回收率等于或高于80%。方法的检出限(LOD)范围为0.002至0.052μg/ L,从而可以按照欧盟(EU)饮用水法规的要求对选定的农药进行检出。

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