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潘闽君, 曹茜, 景明, 李晋阳, 陈家玮. 超声辅助-原位生成离子液体分散液液微萃取结合高效液相色谱法测定水样中的莠去津[J]. 岩矿测试, 2015, 34(3): 353-358. DOI: 10.15898/j.cnki.11-2131/td.2015.03.016
引用本文: 潘闽君, 曹茜, 景明, 李晋阳, 陈家玮. 超声辅助-原位生成离子液体分散液液微萃取结合高效液相色谱法测定水样中的莠去津[J]. 岩矿测试, 2015, 34(3): 353-358. DOI: 10.15898/j.cnki.11-2131/td.2015.03.016
Min-jun PAN, Xi CAO, Ming JING, Jin-yang LI, Jia-wei CHEN. HPLC Determination of Atrazine in Water Using Dispersive Liquid-Liquid Microextraction Based on Ultrasonic-assisted in situ Ionic Liquid Formation[J]. Rock and Mineral Analysis, 2015, 34(3): 353-358. DOI: 10.15898/j.cnki.11-2131/td.2015.03.016
Citation: Min-jun PAN, Xi CAO, Ming JING, Jin-yang LI, Jia-wei CHEN. HPLC Determination of Atrazine in Water Using Dispersive Liquid-Liquid Microextraction Based on Ultrasonic-assisted in situ Ionic Liquid Formation[J]. Rock and Mineral Analysis, 2015, 34(3): 353-358. DOI: 10.15898/j.cnki.11-2131/td.2015.03.016

超声辅助-原位生成离子液体分散液液微萃取结合高效液相色谱法测定水样中的莠去津

HPLC Determination of Atrazine in Water Using Dispersive Liquid-Liquid Microextraction Based on Ultrasonic-assisted in situ Ionic Liquid Formation

  • 摘要: 本文引入绿色溶剂离子液体作为萃取剂, 建立了超声辅助-原位生成离子液体分散液液微萃取水样中莠去津的方法。即处理5 mL水溶液样品, 以80 μL的HMIMCl为萃取剂, 加入400 μL配对离子交换剂双三氟甲磺酰亚胺锂盐(LiNTf2), 通过原位生成的疏水性离子液体HMIMNTf2, 对水中莠去津进行液液微萃取, 经辅助超声10 min后4000 r/min离心8 min, 结合高效液相色谱测定莠去津。莠去津的检出限为0.01 mg/L, 方法线性范围为0.01~0.5 mg/L, 加标回收率(100.4%~106.7%)显著优于直接离子液体分散液液萃取法( < 67%)。这种原位生成离子液体微萃取技术有望应用于更广泛的有机污染物分析检测中。

     

    Abstract: A kind of green solvent, ionic liquid, was introduced as an extracting agent, and a new method of dispersive liquid-liquid microextraction based on ultrasonic-assisted in situ ionic liquid formation (DLLM-UAISLF) was established for the High Performance Liquid Chromatography (HPLC) determination of atrazine in water. Five mL of water was treated using 80 μL of HMimCl as the extracting agent, 400 μL of LiNTf2 as the ion-exchange material, ultrasound time of 10 minutes and centrifuge time of 8 minutes at 4000 r/min. During this process, the droplets of ionic liquid HMimNTf2 were formed in water and the precipitates were then separated for determination of atrazine by HPLC. The detection limit of atrazine is 0.01 mg/L and the detection values range from 0.01 to 0.5 mg/L. The proposed method yielded recoveries of 100.4%-106.7%, which are obviously better than those ( < 67%) of direct liquid-liquid microextraction. This method has potential in the determination of organic pollutants.

     

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