Fan Chen, Liang You, Dong Hongqiang, Ding Guanglong, Zhang Wenbing, Tang Gang, Yang Jiale, Kong Dandan, Wang Deng, Cao Yongsong
College of Plant Protection, China Agricultural University, Beijing, China.
College of Plant Protection, China Agricultural University, Beijing, China.
Anal Chim Acta. 2017 Jul 4;975:20-29. doi: 10.1016/j.aca.2017.04.036. Epub 2017 Apr 26.
In this work, in-situ ionic liquid dispersive liquid-liquid microextraction combined ultrasmall FeO magnetic nanoparticles was developed as a kind of pretreatment method to detect pyrethroid pesticides in water samples. New anion-exchange reagents including Na[DDTC] and Na[N(CN)] were optimized for in-situ extraction pyrethroids, which showed enhanced microextraction performance. Pyrethroids were enriched by hydrophilic ionic liquid [P][Br] (aqueous solution, 200 μL, 0.2 mmol mL) reaction in-situ with anion-exchange reagent Na[N(CN)] (aqueous solution, 300 μL, 0.2 mmol mL) forming hydrophobic ionic liquid as extraction agent in water sample (10 mL). Ultrasmall superparamagnetic iron oxide nanoparticles (30 mg) were used to collect the mixture of ionic liquid and pyrethroids followed by elution with acetonitrile. The extraction of ionic liquid strategies was unique and efficiently fulfilled with high enrichment factors (176-213) and good recoveries (80.20-117.31%). The method was successively applied to the determination of pyrethroid pesticides in different kinds of water samples with the limits of detection ranged from 0.16 to 0.21 μg L. The proposed method is actually nanometer-level microextraction (average size 80 nm) with the advantages of simplicity, rapidity, and sensitivity.
在本研究中,原位离子液体分散液液微萃取结合超小FeO磁性纳米颗粒被开发为一种用于检测水样中拟除虫菊酯类农药的预处理方法。优化了包括Na[DDTC]和Na[N(CN)]在内的新型阴离子交换试剂用于原位萃取拟除虫菊酯类,其表现出增强的微萃取性能。拟除虫菊酯类通过亲水性离子液体[P][Br](水溶液,200 μL,0.2 mmol mL)与阴离子交换试剂Na[N(CN)](水溶液,300 μL,0.2 mmol mL)原位反应,在水样(10 mL)中形成疏水性离子液体作为萃取剂进行富集。超小超顺磁性氧化铁纳米颗粒(30 mg)用于收集离子液体和拟除虫菊酯类的混合物,随后用乙腈洗脱。离子液体萃取策略独特且高效实现,具有高富集因子(176 - 213)和良好回收率(80.20 - 117.31%)。该方法成功应用于不同种类水样中拟除虫菊酯类农药的测定,检测限为0.16至0.21 μg L。所提出的方法实际为纳米级微萃取(平均尺寸80 nm),具有简单、快速和灵敏的优点。