Preparation and evaluation of molecularly imprinted ionic liquids polymer as sorbent for on-line solid-phase extraction of chlorsulfuron in environmental water samples

2011 ◽  
Vol 1218 (37) ◽  
pp. 6271-6277 ◽  
Author(s):  
Lu Guo ◽  
Qiliang Deng ◽  
Guozhen Fang ◽  
Wei Gao ◽  
Shuo Wang
Talanta ◽  
2019 ◽  
Vol 196 ◽  
pp. 47-53 ◽  
Author(s):  
Xiaoli Sun ◽  
Muhua Wang ◽  
Junyu Peng ◽  
Luoxing Yang ◽  
Xueli Wang ◽  
...  

2021 ◽  
Author(s):  
Zhenjie Yin ◽  
Sheng Liu ◽  
Xinxin Jin ◽  
Yajie Ma ◽  
Hong Yu

Abstract With the increasing emphasis on the toxicity of ionic liquids, it is imperative to develop detection methods for ionic liquids in complex environments. A new method for the analysis of hydroxyl functionalized imidazolium ionic liquids in complex environmental water samples by using ion chromatography and solid-phase extraction was developed. Under the selected chromatographic conditions, the complete separation of the two analytes was achieved in 14.0 min. The linear and repetitive data of the approach for the analysis of the two cations by ion chromatography meet the requirements of quantitative analysis. The extraction of [HEMIm]+ and [HPMIm]+ in water samples by ion-exchange solid-phase extraction and reversed-phase solid-phase extraction was compared. The results show that the enrichment and purification of two target cations can be better achieved using ion-exchange solid-phase extraction approach, and the enrichment multiple was 50 times. The method was used to determine the target cations in two river waters. The recovery of standard addition was between 82.5% and 96.0%, the detection limit was less than 0.01 mg/L, and inter-assay RSD was less than 2.5%. The method is simple, accurate and reliable. It is suitable for the determination of hydroxyl functionalized imidazolium ionic liquid cations in environmental water samples.


Separations ◽  
2020 ◽  
Vol 7 (1) ◽  
pp. 14
Author(s):  
Hyun-Jeoung Lee ◽  
Chansik Kim ◽  
Hong-Duck Ryu ◽  
Eu Gene Chung ◽  
Dongseok Shin ◽  
...  

Pesticides and veterinary pharmaceuticals are used for effective crop production and prevention of livestock diseases; these chemicals are released into the environment via various pathways. Although the chemicals are typically present in trace amounts post-release, they could disturb aquatic ecosystems and public health through resistance development toward drugs or diseases, e.g., reproductive disorders. Thus, the residues of pesticides and veterinary pharmaceuticals in the environment must be managed and monitored. To that end, we developed a simultaneous analysis method for 41 target chemicals in environmental water samples using ultra-high-performance liquid chromatography (UHPLC)–quadrupole-orbitrap high-resolution mass spectrometry (HRMS) coupled with an on-line solid-phase extraction system. Calibration curves for determining linearity were constructed for 10–750 ng∙L−1, and the coefficient of determination for each chemical exceeded 0.99. The method’s detection and quantitation limits were 0.32–1.72 ng∙L−1 and 1.02–5.47 ng∙L−1, respectively. The on-line solid-phase extraction system exhibited excellent method reproducibility and reduced experimental error. As the proposed method is applicable to the monitoring of pesticides and veterinary pharmaceuticals in surface water and groundwater samples acquired near agricultural areas, it allows for the management of chemicals released into the environment.


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