Separation and quantification of diazinon in water samples using liquid-phase microextraction-based effervescent tablet-assisted switchable solvent method coupled to gas chromatography-flame ionization detection

被引:1
|
作者
Kakaei, Hojatollah [1 ,2 ]
Shahtaheri, Seyed Jamaleddin [3 ,4 ]
Abdi, Khosrou [5 ]
Rahimi Kakavandi, Nader [1 ]
机构
[1] Ilam Univ Med Sci, Sch Hlth, Dept Occupat Hlth Engn, Ilam, Iran
[2] Ilam Univ Med Sci, Hlth & Environm Res Ctr, Ilam, Iran
[3] Univ Tehran Med Sci, Sch Hlth, Dept Occupat Hlth Engn, Tehran, Iran
[4] Univ Tehran Med Sci, Inst Environm Res Ctr Water Qual Res, Tehran, Iran
[5] Univ Tehran Med Sci, Sch Pharm, Dept Nucl Pharmaceut Grp, Tehran, Iran
关键词
diazinon; effervescent tablet; gas chromatography-flame ionization detection; liquid-phase microextraction; surface water sample; switchable solvent; ORGANOPHOSPHORUS PESTICIDES; ORGANOCHLORINE PESTICIDES; MASS-SPECTROMETRY; COMBINATION; RESIDUES; HONEY; APPLE;
D O I
10.1002/bmc.5624
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This study used a liquid-phase microextraction-based effervescent tablet-assisted switchable solvent method coupled to gas chromatography-flame ionization detection as an eco-efficient, convenient-to-use, cost-effective, sensitive, rapid, and efficient method for extracting, preconcentrating, and quantifying trace amounts of diazinon in river water samples. As a switchable solvent, triethylamine (TEA) was used. In situ generation of CO2 using effervescent tablet containing Na2CO3 and citric acid changed the hydrophobic TEA to the hydrophilic protonated triethylamine carbonate (P-TEA-C). CO2 removal from the specimen solution using NaOH caused P-TEA-C to be converted into TEA and led to phase separation, during which diazinon was extracted into the TEA phase. The salting-out process was helpful in enhancing extraction efficiency. In addition, a number of significant parameters that affect extraction recovery were examined. Under optimum conditions, the limit of detection and limit of quantitation were 0.06 and 0.2 ng/ml, respectively. The extraction recovery percentage and pre-concentration factor were obtained at 95 and 190%, respectively, and the precision (inter- and intra-day, relative standard deviation %, n = 5) was <5%.
引用
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页数:9
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