Trace determination of organophosphate esters in environmental water samples with an ionogel-based nanoconfined ionic liquid fiber coating for solid-phase microextraction with gas chromatography and flame photometric detection

被引:22
|
作者
Pang, Long [1 ]
Pang, Rong [2 ]
Ge, Liming [1 ]
Zheng, Liqing [3 ]
Zhao, Jihong [1 ]
Zhang, Hongzhong [1 ]
机构
[1] Zhengzhou Univ Light Ind, Dept Mat & Chem Engn, Collaborat Innovat Ctr Environm Pollut Control &, Zhengzhou, Peoples R China
[2] Huanghe Sci & Technol Coll, Dept Med, Zhengzhou, Peoples R China
[3] Henan Normal Univ, Sch Chem & Environm Sci, Xinxiang, Peoples R China
关键词
Ionic liquids; Ionogels; Organophosphate esters; Solid-phase microextraction; IONIZATION DETECTION; TREATMENT PLANTS; RETARDANTS; PLASTICIZERS; CHINA; TECHNOLOGY; BENZENE; TOLUENE; URINE;
D O I
10.1002/jssc.201600662
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Organophosphate esters, widely used as flame retardants and plasticizers, are regarded as a class of emerging pollutants. In this work, a novel approach was developed for the fabrication of a solid-phase microextraction fiber by using hybrid silica-based materials with immobilized ionic liquids with sol-gel technology, and the prepared solid-phase microextraction fiber was then coupled with gas chromatography and flame photometric detection for the analysis of six organophosphate esters. The high loading of 1-hexadecyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide was confined within the hybrid network. The developed solid-phase microextraction fiber possesses a coating thickness of similar to 35 mu m with good thermal stability and long lifetime. The parameters affecting the extraction efficiency such as extraction time, temperature, pH, and ionic strength of the sample solution were optimized. Under the optimized conditions, the limits of detection were in the range of 0.04-0.95 mu g L-1, and the precision of the method assessed with repeatability and reproducibility of (RSD%) <13 and <29%, respectively. The proposed method was successfully applied to determine the six organophosphate esters in three real water samples, with recoveries in the range of 64.8-125.4% at two different spiking concentration levels. As a result, the proposed method demonstrated its potential for application in trace determination of organophosphate esters in actual water samples.
引用
收藏
页码:4415 / 4421
页数:7
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