In situ rapid magnetic solid-phase extraction coupled with HPLC-ICP-MS for mercury speciation in environmental water

2016 ◽  
Vol 126 ◽  
pp. 25-31 ◽  
Author(s):  
Shengxiao Zhang ◽  
Hao Luo ◽  
Yuanyuan Zhang ◽  
Xiaoyan Li ◽  
Junshen Liu ◽  
...  
2020 ◽  
Vol 12 (40) ◽  
pp. 4906-4912
Author(s):  
Qingsong Zhang ◽  
Guangyang Liu ◽  
Xiaolin Cao ◽  
Jungang Yin ◽  
Ziping Zhang

In this paper, magnetic ZIF-67 composites were prepared by an in situ method and utilized in the magnetic solid-phase extraction of phthalate esters.


2021 ◽  
Author(s):  
Xinyi Li ◽  
Bingzhi Li ◽  
Min Chen ◽  
Mengmeng Yan ◽  
Xiaolin Cao ◽  
...  

In this paper, magnetic zeolitic imidazolate framework-8 composites were synthesized by the simple in-situ method and then firstly used as adsorbent in magnetic solid-phase extraction for extracting multiple strobilurin fungicides....


Author(s):  
Yifeng He ◽  
Man He ◽  
Beibei Chen ◽  
Bin Hu

A novel sulfur-containing functional core-shell magnetic porous organic polymer (Fe3O4@BD-TpMA-S-SH MOPs) was synthesized as magnetic solid phase extraction (MSPE) sorbent for mercury speciation followed by high performance liquid chromatography (HPLC)...


Materials ◽  
2020 ◽  
Vol 13 (24) ◽  
pp. 5729
Author(s):  
Jiping Ma ◽  
Liwei Hou ◽  
Gege Wu ◽  
Liyan Wang ◽  
Xiaoyan Wang ◽  
...  

Magnetic multi-walled carbon nanotubes were prepared as magnetic solid-phase extraction (MSPE) adsorbent for the enrichment of six heterocyclic pesticides in environmental water samples, including imidacloprid, triadimefon, fipronil, flusilazole, chlorfenapyr and fenpyroximate. Then six heterocyclic pesticides were separated and determined by high-performance liquid chromatography-diode-array detector (HPLC-DAD). Major factors influencing MSPE efficiency, including the dose of mag-multi-walled carbon nanotubes (mag-MWCNTs), extraction time, solution pH, salt concentration, type and volume of eluent and desorption time were investigated. Under the optimized conditions, the enrichment factor of the method reached to 250. The linearity was achieved within 0.05–10.0 μg/L for imidacloprid and chlorfenapyr, 0.10–10.0 μg/L for fipronil, flusilazole, triadimefon and fenpyroximate. Limits of detection were in the range of 0.01–0.03 μg/L. Good precision at three spiked levels were 1.1–11.2% (intra-day) and 1.7–11.0% (inter-day) with relative standard deviation of peak area, respectively. The developed method was utilized to analyze tap water, river water and reservoir water samples and recoveries at three spiked concentration levels ranged from 72.2% to 107.5%. The method was proved to be a convenient, rapid and practical method for sensitive determination of heterocyclic pesticides.


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