Deep eutectic solvent-based dispersive liquid-liquid microextraction followed by smartphone digital image colorimetry for the determination of carbofuran in water samples

被引:1
|
作者
Zhao, Luyao [1 ,2 ]
Wang, Min [1 ]
Wang, Jiadong [3 ]
Wu, Jing [2 ]
Zhang, Zhuoting [1 ]
Jing, Xu [1 ,2 ]
Wang, Xiaowen [1 ]
机构
[1] Shanxi Agr Univ, Coll Food Sci & Engn, Taigu 030801, Shanxi, Peoples R China
[2] Nankai Univ, Sch Med, Tianjin Key Lab Food Sci & Hlth, Tianjin 300071, Peoples R China
[3] Xinyang Agr & Forestry Univ, Sch Pharmaceut Engn, Xinyang, Peoples R China
基金
中国国家自然科学基金;
关键词
SOLID-PHASE EXTRACTION; PESTICIDES; 3-HYDROXY-CARBOFURAN; RESIDUES;
D O I
10.1039/d2ay01861f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A detection method of carbofuran (CBF) in water samples was reported using deep eutectic solvent (DES)-based dispersive liquid-liquid microextraction (DLLME) combined with digital image colorimetry (DIC), which was environmentally friendly, solvent-saving, rapid, and convenient. Under alkaline conditions, the green and multifunctional extractant DESs dissociated into linalool and heptanoic acid, and CBF was hydrolyzed to 2,3-dihydro-2,2-dimethyl-7-benzofuranol and further coupled with fast blue BB salt to form an azo derivative. Heptanoic acid led to the dispersion of linalool to extract the orange-red azo derivative; DIC was used for quantitative analysis using a smartphone with its associated ease of data-acquisition. This experiment optimized the types, molar ratios, and volumes of DESs and the amounts of sodium carbonate and sodium chloride. Under optimal conditions, the limits of detection (LOD) and quantitation (LOQ) were 0.024-0.032 mg L-1 and 0.081-0.108 mg L-1, respectively. The extraction recoveries in real samples (tap, pond, and river water) were 92.4-101.0% with a relative standard deviation below 4.6%. This method has successfully analyzed CBF in different water samples and shows prospects for the monitoring and control of CBF residues in other environmental samples.
引用
收藏
页码:648 / 654
页数:7
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