A sensitive method for the determination of gold and palladium based on dispersive liquid-liquid microextraction combined with flame atomic absorption spectrometric determination using N-(6-morpholin-4-ylpyridin-3-yl)-N '-phenylthiourea


RSC ADVANCES, vol.6, no.9, pp.6896-6904, 2016 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 6 Issue: 9
  • Publication Date: 2016
  • Doi Number: 10.1039/c5ra26575d
  • Journal Name: RSC ADVANCES
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.6896-6904
  • Karadeniz Technical University Affiliated: Yes


A new method for the determination of gold and palladium was developed by dispersive liquid-liquid microextraction separation-preconcentration and flame atomic absorption spectrometry detection. In the proposed approach, N-(6-morpholin-4-ylpyridin-3-yl)-N'-phenylthiourea (MPPT) was synthesized as a complexing agent. The complexation ability of the MPPT was explored by examining the effect of a series of heavy metal ions, including Mn2+, Pd2+, Ni2+, Cd2+, Co2+, Cu2+, Au3+, Pb2+, Zn2+ and Fe3+, using the DLLME procedure. The MPPT exhibited pronounced selectivity toward Pd2+ and Au3+ ions at different pH levels. Factors influencing the extraction efficiency and complex formation were examined, i.e. the pH of the sample solution, the concentration of the chelating agent, the extraction and dispersive solvent type and volume, the sample volume, and foreign ions, etc. Optimal conditions for quantitative recoveries were pH 5.5 for gold and pH 1.5 for palladium, 125 mu L of % 0.4 MPPT, 1200 mu L of methanol and 125 mu L of carbon tetrachloride. The presented method showed a good linearity within a range of 30-230 and 25-200 mu g L-1 with the detection limits of 1.75 and 1.65 mu g L-1 for Au and Pd, respectively. The relative standard deviation (RSD) was below 2.8% at 50 mu g L-1 for both ions (n = 10). The developed method was simple, fast, cost efficient, and sensitive for the extraction and preconcentration of gold and palladium in samples of liquids (sea, stream water) and solids (stream sediment, ores, and electronic waste).