4.6 Article

Determination of malachite green and crystal violet in environmental water using temperature-controlled ionic liquid dispersive liquid-liquid microextraction coupled with high performance liquid chromatography

期刊

ANALYTICAL METHODS
卷 4, 期 2, 页码 429-433

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ay05665h

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资金

  1. National Natural Science Foundation of China [21107036]
  2. State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology [HCK201017]
  3. Initial Research Fund of Highly Specialized Personnel from Jiangsu University [1281220014]
  4. National Water Pollution Control and Treatment Project [2008ZX07101-006-05]
  5. Foundation of State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences [KF2010-22]

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Temperature-controlled ionic liquid dispersive liquid-liquid microextraction (TC-IL-DLLME) was introduced to analyze malachite green (MG) and crystal violet (CV) in environmental water by coupling with high performance liquid chromatography (HPLC). In the method, 1-octyl-3-methylimidazolium hexafluorophosphate ([C8MIM][PF6]) and methanol were selected as appropriate extraction and dispersive solvents, respectively. Target compounds were extracted into the IL phase (dispersed completely in the aqueous phase) at a proper temperature. Several other parameters that could affect extraction performance were optimized, such as IL volume, sample pH, salinity, extraction time, temperature and centrifuging velocity. Under the optimum conditions (IL volume, 80 mu L; sample pH, 4; salinity, 20% sodium chloride; extraction time, 50 min; temperature, 70 degrees C; centrifuging velocity, 1500 rpm), the established method offered: (i) good linear range (0.25-20 mu g L-1); (ii) low detection limits (MG, 0.086 mu g L-1; CV, 0.030 mu g L-1); (iii) good reproducibility (relative standard deviation, MG, 9.4%; CV, 7.6%; n = 5) and good recoveries (91.7% for MG and 97.2% for CV, respectively; n 5); (iv) high enrichment factor (254 for MG, 276 for CV), which makes the method suitable to monitor low concentrations of MG and CV in aqueous systems.

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