Reliable methods for determination of triazine herbicides and their degradation products in seawater and marine sediments using liquid chromatography-tandem mass spectrometry

被引:18
作者
Rodriguez-Gonzalez, N. [1 ]
Uzal-Varela, R. [1 ]
Gonzalez-Castro, M. J. [1 ]
Muniategui-Lorenzo, S. [1 ]
Beceiro-Gonzalez, E. [1 ]
机构
[1] Univ A Coruna, Dept Quim Analit, Grp Quim Analit Aplicada QANAP, Inst Univ Medio Ambiente IUMA,Fac Ciencias, Campus Coruna, La Coruna 15071, Spain
关键词
Triazines; Degradation products; Seawater; Sediments; Liquid chromatography; Mass spectrometry; SOLID-PHASE EXTRACTION; DEALKYLATED METABOLITES; PESTICIDE-RESIDUES; POLAR PESTICIDES; MAJOR HYDROXY; WATER; TERBUTHYLAZINE; SAMPLES; DISPERSION;
D O I
10.1007/s11356-017-8389-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Triazines and their degradation products are transported to the aquatic environment, and once there, the probability to reach the marine environment is very high. In this paper, solid phase extraction (SPE) and extraction by matrix solid phase dispersion (MSPD) to analyse nine triazines (ametryn, atrazine, cyanazine, prometryn, propazine, simazine, simetryn, terbuthylazine and terbutryn) and eight degradation products (desethylatrazine, desethyldesisopropylatrazine, desethyl-2-hydroxyatrazine, desethylterbuthylazine, desisopropylatrazine, desisopropyl-2-hydroxyatrazine, 2-hydroxyatrazine and 2-hidroxyterbuthylazine) in seawater and marine sediments samples were used. The analysis was carried out using liquid chromatography with tandem mass spectrometry (LC-ESI-MS/MS). The methods were optimized and validated to achieve a selective and sensitive determination of the analytes from different sample, regardless of its complexity. Under the optimum conditions, the proposed methods provided adequate limits of quantification (0.05-0.45 mu g L-1 and 0.23-4.26 mu g kg(-1) in seawater and marine sediments, respectively). Intra-and inter-day relative standard deviation were below 1.41% for all compounds. Recoveries were evaluated, and acceptable values that ranged from 87.5-99.4 and 60.9-99.7% for the seawater and sediment samples, respectively, were obtained. The proposed methods were applied to the analysis of the target compounds in seawater samples and marine sediments from a coastal area of Galicia (NW of Spain).
引用
收藏
页码:7764 / 7775
页数:12
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