4.7 Article

Mercury determination in urine samples by gold nanostructured screen-printed carbon electrodes after vortex-assisted ionic liquid dispersive liquid-liquid microextraction

期刊

ANALYTICA CHIMICA ACTA
卷 915, 期 -, 页码 49-55

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2016.02.028

关键词

Vortex-assisted dispersive liquid-liquid microextraction; Ionic liquid; Mercury; Screen-printed electrodes; Urine samples

资金

  1. Spanish Ministry of Science and Innovation [CTQ2011-23968, CTQ2011-24560]
  2. Generalitat Valenciana (Spain) [ACOMP/2013/072, GVA/2014/096, PROMETEO/2013/038]
  3. University of Alicante (Spain) [GRE12-45]
  4. Ministry of Education [FPU13/03125]

向作者/读者索取更多资源

A novel approach is presented to determine mercury in urine samples, employing vortex-assisted ionic liquid dispersive liquid-liquid microextraction and microvolume back-extraction to prepare samples, and screen-printed electrodes modified with gold nanoparticles for voltammetric analysis. Mercury was extracted directly from non-digested urine samples in a water-immiscible ionic liquid, being back-extracted into an acidic aqueous solution. Subsequently, it was determined using gold nanoparticle-modified screen-printed electrodes. Under optimized microextraction conditions, standard addition calibration was applied to urine samples containing 5, 10 and 15 mu g L-1 of mercury. Standard addition calibration curves using standards between 0 and 20 mu g L-1 gave a high level of linearity with correlation coefficients ranging from 0.990 to 0.999 (N = 5). The limit of detection was empirical and statistically evaluated, obtaining values that ranged from 0.5 to 1.5 mu g L-1, and from 1.1 to 1.3 mu g L-1, respectively, which are significantly lower than the threshold level established by the World Health Organization for normal mercury content in urine (i.e., 10-20 mu g L-1). A certified reference material (REC-8848/Level II) was analyzed to assess method accuracy finding 87% and 3 mu g L-1 as the recovery (trueness) and standard deviation values, respectively. Finally, the method was used to analyze spiked urine samples, obtaining good agreement between spiked and found concentrations (recovery ranged from 97 to 100%). (C) 2016 Elsevier B.V. All rights reserved.

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