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Deep eutectic solvent-based dispersive liquid-liquid microextraction followed by smartphone digital image colorimetry for the determination of carbofuran in water samples.
Zhao, Luyao; Wang, Min; Wang, Jiadong; Wu, Jing; Zhang, Zhuoting; Jing, Xu; Wang, Xiaowen.
Afiliação
  • Zhao L; College of Food Science and Engineering, Shanxi Agricultural University, Taigu, Shanxi 030801, China. x.jing@vip.163.com.
  • Wang M; Tianjin Key Laboratory of Food Science and Health, School of Medicine, Nankai University, Tianjin 300071, China.
  • Wang J; College of Food Science and Engineering, Shanxi Agricultural University, Taigu, Shanxi 030801, China. x.jing@vip.163.com.
  • Wu J; School of Pharmaceutical Engineering, Xinyang Agriculture and Forestry University, Xinyang 46400, China.
  • Zhang Z; Tianjin Key Laboratory of Food Science and Health, School of Medicine, Nankai University, Tianjin 300071, China.
  • Jing X; College of Food Science and Engineering, Shanxi Agricultural University, Taigu, Shanxi 030801, China. x.jing@vip.163.com.
  • Wang X; College of Food Science and Engineering, Shanxi Agricultural University, Taigu, Shanxi 030801, China. x.jing@vip.163.com.
Anal Methods ; 15(5): 648-654, 2023 Feb 02.
Article em En | MEDLINE | ID: mdl-36651811
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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article