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多残留农药分析用候选检测器的二维气相色谱法基准测试。

Benchmarking of candidate detectors for multiresidue analysis of pesticides by comprehensive two-dimensional gas chromatography.

机构信息

INRA, UR370 QuaPA, Micro-contaminants, Aroma and Separation Science Group, 63122 Saint-Genès-Champanelle, France; Centre for Green Chemistry School of Chemistry, Monash University, Wellington Road, Clayton, Victoria 3800, Australia.

出版信息

J Chromatogr A. 2013 Oct 11;1311:140-8. doi: 10.1016/j.chroma.2013.08.011. Epub 2013 Aug 8.

Abstract

The present study discusses the relevance, performance and complementarities of flame photometric detector in phosphorus (FPD/P) and sulfur (FPD/S) modes, micro electron capture detector (μECD), nitrogen phosphorus detector (NPD), flame ionization detector (FID) and time-of-flight mass spectrometer (TOF/MS) for the comprehensive two-dimensional gas chromatography (GC×GC) analysis of pesticides. A mix of 41 pesticides including organophosphorus pesticides, synthetic pyrethroids and fungicides was investigated in order to benchmark GC×GC systems in terms of linearity (R(2)), limits of detection (LOD), and peak shape measures (widths and asymmetries). A mixture of pesticides which contained the heteroatoms phosphorus, sulfur, nitrogen and one or several halogens, was used to acquire a comparative data set to monitor relative detector performances. GC×GC datasets were systematically compared to their GC counterpart acquired with an optimized one-dimensional GC configuration. Compared with FID, considered the most appropriate detector in terms of suitability for GC×GC, the element-selective detector FPD/P and μECD best met the peak widths (0.13-0.27s for FPD/P; 0.22-0.26s for μECD) and tailing factors (0.99-1.66 for FPD/P; 1.32-1.52 for μECD); NPD exhibited similar peak widths (0.23-0.30s), but exceeded those of the above detectors for tailing factors (1.97-2.13). These three detectors had improved detection limits of 3-7 times and 4-20 times lower LODs in GC×GC mode compared with FID and TOF-MS, respectively. In contrast FPD/S had poor peak shape (tailing factor 3.36-5.12) and much lower sensitivity (10-20 fold lower compared to FPD/P). In general, element-selective detectors with favorable detection metrics can be considered viable alternatives for pesticide determination using GC×GC in complex matrices. The controversial issue of sensitivity enhancement in GC×GC was considered for optimized GC and GC×GC operation. For all detectors, we found no significant LOD enhancement in GC×GC.

摘要

本研究讨论了火焰光度检测器(FPD/P 和 FPD/S 模式)、微电子捕获检测器(μECD)、氮磷检测器(NPD)、火焰电离检测器(FID)和飞行时间质谱(TOF/MS)在农药的全二维气相色谱(GC×GC)分析中的相关性、性能和互补性。为了在二维气相色谱系统的线性度(R²)、检测限(LOD)和峰形参数(峰宽和不对称性)方面对其进行基准测试,研究中使用了 41 种农药的混合物,包括有机磷农药、合成拟除虫菊酯和杀菌剂。使用含有磷、硫、氮和一个或多个卤素杂原子的农药混合物来获得一个比较数据集,以监测相对检测器的性能。GC×GC 数据集与使用优化一维 GC 配置获得的 GC 数据集进行了系统比较。与 FID 相比,FPD/P 和 μECD 这两种元素选择性检测器在适用于 GC×GC 方面被认为是最合适的检测器,它们的峰宽(FPD/P 为 0.13-0.27s;μECD 为 0.22-0.26s)和拖尾因子(FPD/P 为 0.99-1.66;μECD 为 1.32-1.52)最佳;NPD 的峰宽相似(0.23-0.30s),但拖尾因子高于上述检测器(1.97-2.13)。与 FID 和 TOF-MS 相比,这三种检测器在 GC×GC 模式下的检测限提高了 3-7 倍和 4-20 倍。相比之下,FPD/S 的峰形较差(拖尾因子为 3.36-5.12),灵敏度低得多(与 FPD/P 相比低 10-20 倍)。一般来说,具有良好检测指标的元素选择性检测器可被视为在复杂基质中使用 GC×GC 进行农药测定的可行替代方法。对于优化 GC 和 GC×GC 操作,我们考虑了 GC×GC 中灵敏度增强的争议问题。对于所有检测器,我们都没有发现 GC×GC 中存在显著的检测限增强。

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