Demonstrates a method for detecting trace Mo(VI) in water, indicating its effectiveness for environmental monitoring.
An adsorptive stripping voltammetric method for the determination of ultra trace amounts of Mo(VI) using an electrode based on a mixture of carbon nanotubes and spherical glassy carbon (CNT/SGC) was developed. The electrode was modified by depositing a lead film in situ during each measurement cycle. In a supporting electrolyte containing 0.2 mol/L of acetic buffer pH = 5.3; 0.2 mmol/L of Pb(II); and 0.15 mmol/L of cupferron, the stripping response observed at −0.62 V was proportional to the Mo(VI) concentration within the range of 7 nmol/L to 0.6 µmol/L. The measurement protocol involved a 20 s electrode modification followed by a 30 s adsorption of Mo(VI)–cupferron complexes. The limit of detection was found to be 2.5 nmol/L with a correlation coefficient of 0.997. The method has been applied to the determination of Mo(VI) in mineral water samples.
No takes yet. Share an insight, caveat, or question.
Grabarczyk et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: