Effective extraction of triazines from environmental water samples using magnetism-enhanced monolith-based in-tube solid phase microextraction

被引:43
作者
Mei, Meng [1 ]
Huang, Xiaojia [1 ]
Yang, Xiaodong [2 ]
Luo, Qing [3 ]
机构
[1] Xiamen Univ, Coll Environm & Ecol, Minist Educ Coastal & Wetland Ecosyst, State Key Lab Marine Environm Sci,Key Lab, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[3] Xiamen Univ, Coll Mat, Dept Mat Sci & Engn, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
Magnetism-enhanced in-tube solid phase microextraction; Monolithic capillary column; Triazines; Sample pretreatment; Water; MOLECULARLY IMPRINTED POLYMER; LIQUID-LIQUID MICROEXTRACTION; MASS-SPECTROMETRY; SORPTIVE EXTRACTION; HERBICIDES; ATRAZINE; PRECONCENTRATION; SIMAZINE; FIBER; GC;
D O I
10.1016/j.aca.2016.08.001
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This article reports on the effective extraction of triazines from environmental water samples using magnetism-enhanced monolith-based in-tube solid phase microextraction (ME-MB/IT-SPME). Firstly, monolithic poly (octyl methacrylate-co-ethyleneglycol dimethacrylate) capillary column doped with magnetic nanoparticles was synthesized inside a fused silica. After that, the monolithic capillary column was placed inside a magnetic coil that allowed the exertion of a variable magnetic field during adsorption and desorption steps. The effects of intensity of magnetic field, adsorption and desorption flow rate, volume of sample and desorption solvent, pH value and ionic strength in sample matrix on the performance of ME-MB/IT-SPME for triazines were investigated in details. Under the optimized conditions, the developed ME-MB/IT-SPME showed satisfactory quantitative extraction efficiencies of the target analytes between 64.8% and 99.7%. At the same time, the ME-MB/IT-SPME was combined with high-performance liquid chromatography with diode array detection to detect six triazines in water samples. The limits of detection (S/N = 3) and limits of quantification (S/N = 10) were in the ranges of 0.074-0.23 mu g/L and 0.24-0.68 mu g/L, respectively. The precision of the proposed method was evaluated in terms of intra-and inter-assay variability calculated as relative standard deviation, and it was found that the values were all below 10%. Finally, the developed method was successfully applied for environmental water samples such as farmland, lake and river water with spiked recoveries in the range of 70.7-119%. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 79
页数:11
相关论文
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