4.7 Article

Displacement solid-phase extraction on mercapto-functionalized magnetite microspheres for inductively coupled plasma mass spectrometric determination of trace noble metals

Journal

ANALYTICA CHIMICA ACTA
Volume 692, Issue 1-2, Pages 42-49

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2011.02.055

Keywords

Displacement solid-phase extraction; Inductively coupled plasma mass spectrometry; Noble metals; Magnetic immobilization

Funding

  1. National Natural Science Foundation of China [20935001, 20705014, 20975054]
  2. Specialized Research Fund for the Doctoral Program of Higher Education [20070055055]
  3. Chinese Ministry of Education [109040]
  4. Fok Ying Tong Education Foundation [114041]
  5. Tianjin Natural Science Foundation [08JCYBJC00600, 09JCYBJC14200]
  6. Program for New Century Excellent Talents [NCET-09-0482]
  7. A Foundation for the Author of National Excellent Doctoral Dissertation of PR China [FANEDD-201023]

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A flow injection online displacement solid-phase extraction (DSPE) via magnetic immobilization of mercapto-functionalized magnetite microspheres onto the inner walls of a knotted reactor (KR) coupled with inductively coupled plasma mass spectrometry was developed for selective preconcentration and determination of trace noble metals (Ru, Rh, Pd, Pt, Ir and Au) in complex matrices. Online DSPE of 2.7 mL aqueous solution gave the enhancement factors of 32-46 for the six noble metals in comparison with direct nebulization of aqueous sample solution, and the detection limits (3 s) of 2.1 ng L-1 for Ru, 1.9 ng L-1 for Rh, 2.5 ng L-1 for Pd, 1.8 ng L-1 for Ir, 1.9 ng L-1 for Pt and 1.7 ng L-1 for Au. The sample throughput of the developed method was about 20 samples h(-1), and the relative standard deviation for eleven replicate determinations of the noble metals at the 30 ng L-1 level ranged from 1.2% to 2.1%. The recoveries of Ru, Rh, Pd, Pt, It and Au still maintained 90% even after successive 140 cycles of DSPE. The developed method was successfully applied to selective determination of trace Ru, Rh, Pd, Pt, Ir and Au in complex matrices. (C) 2011 Elsevier B.V. All rights reserved.

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