4.7 Article

Spectrophotometric determination of mercury(II) ions based on their stimulation effect on the peroxidase-like activity of molybdenum disulfide nanosheets

Journal

MICROCHIMICA ACTA
Volume 183, Issue 8, Pages 2481-2489

Publisher

SPRINGER WIEN
DOI: 10.1007/s00604-016-1886-4

Keywords

Peroxidase mimic; Spectrophotometric assay; Molybdenum disulfide nanosheets; Surface charge effect; Mercury(II) detection

Funding

  1. Post-Doctoral Science Foundation of China [2013 M542393]
  2. Fundamental Research Fund for the Central Universities [lzujbky-2014-69]
  3. Applied Basic Research Project of Qinghai Province [2015-ZJ-783]

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The authors describe a colorimetric method for the determination of Hg(II) ions by exploiting the peroxidase-lile activity of few-layered MoS2 nanosheets (MoS2-NSs). These were prepared by sonication-induced exfoliation of bulk MoS2 crystals in aqueous surfactant solution. The MoS2-NSs were found to acts as a peroxidase mimic that is capable of oxidizing the substrate 3,3',5,5'-tetramethylbenzidine (TMB) in the presence of hydrogen peroxide (H2O2) to give a blue product with an absorption maximum at 652 nm. The addition of Hg(II) strongly accelerates the kinetics of this reaction. It is shown that the enzyme mimic possesses a high affinity for TMB and a lower pseudo-Michaelis-Menten constant. The stimulating effect of Hg(II) is seriously influenced by the change of surface charge. The use of nanosheets covered with (negatively charged) polystyrene sulfonate results in a decrease in the formation of blue dye, while those covered with (cationic) poly(diallyldimethyl ammonium) ions cause a small increase. Under optimal conditions, the peroxidase-like activity of MoS2-NSs is affected by Hg(II) in the 2.0 to 200 mu M concentration range. The method has a detection limit (LOD) of 0.5 mu M which is much below the allowed level in cosmetics (1 ppm; ca. 5 mu M). The method display excellent sensitivity, selectivity and stability. It was applied to the determination of total mercury in cosmetic samples, and results compared well with results obtained by ICP-AES.

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