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Determination of triazine herbicides in fresh vegetables by dynamic microwave-assisted extraction coupled with homogeneous ionic liquid microextraction high performance liquid chromatography
被引:30
|作者:
Wu, Lijie
[1
]
Hu, Mingzhu
[1
]
Li, Zhanchao
[1
]
Song, Ying
[1
]
Yu, Cui
[2
]
Zhang, Yupu
[3
]
Zhang, Hanqi
[1
]
Yu, Aimin
[1
]
Ma, Qiang
[4
]
Wang, Ziming
[1
]
机构:
[1] Jilin Univ, Coll Chem, Changchun 130012, Peoples R China
[2] Yanching Inst Technol, Sch Chem & Mat Engn, Langfang 065201, Peoples R China
[3] Jilin Prov Tobacco Prod Qual Supervis & Inspect S, Changchun 130062, Peoples R China
[4] Chinese Acad Inspect & Quarantine, Beijing 100123, Peoples R China
基金:
中国博士后科学基金;
中国国家自然科学基金;
关键词:
Dynamic microwave-assisted extraction;
Homogeneous ionic liquid microextraction;
In-situ metathesis reaction;
High-performance liquid chromatography;
Triazine herbicides;
SOLID-PHASE EXTRACTION;
LARGE-VOLUME INJECTION;
ENVIRONMENTAL WATER SAMPLES;
GAS-CHROMATOGRAPHY;
MASS-SPECTROMETRY;
NITROGEN-PHOSPHORUS;
PESTICIDES;
DERIVATIZATION;
PHENYLUREA;
ATRAZINE;
D O I:
10.1007/s00216-014-8393-4
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
A novel extraction method, dynamic microwave-assisted extraction coupled with homogeneous ionic liquid microextraction, was developed for the determination of triazine herbicides, including desmetryn, terbumeton, propazine, terbuthylazine, dimethametryn, and dipropetryn in fresh vegetable samples by high performance liquid chromatography (HPLC). In the developed method, 120 mu L of 1-butyl-3-methylimidazolium tetrafluoroborate ([C4MIM][BF4]) was added to 10 mL of aqueous solution containing 0.3 g of NaCl to obtained the extraction solvent. Six triazines could be extracted completely within 4 min by the present method. Then, [NH4][PF6] was added into the extract to form a water-insoluble ionic liquid [C4MIM][PF6] via a simple metathesis reaction, and the analytes were enriched into the ionic liquid phase. After centrifugation and dilution with acetonitrile, the resulting solution was analyzed directly by HPLC. The effects of some experimental parameters, including type and volume of ionic liquid, volume of extraction solvent, amount of ion-pairing agent [NH4][PF6], salt concentration, microwave power, and flow rate of extraction solvent on the extraction efficiency were investigated and optimized. Under the optimum experimental conditions, the linearity for determining the analytes was in the range of 2.50-250.00 mu g kg(-1), with the correlation coefficients ranging from 0.9989 to 0.9999. When the present method was applied to the analysis of vegetable samples, satisfactory recoveries were obtained in the range of 76.8 %-106.9 %, and relative standard deviations were lower than 9.8 %.
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页码:1753 / 1762
页数:10
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