A New Spectrophotometric Method for Hydrogen Sulphide Through Electrolytically Generated Mn(III) With O‐Tolidine

Abstract

A simple, sensitive and economical spectrophotometric method for the determination of hydrogen sulphide is developed. The method is based on a redox reaction in that Mn(III) generated electrolytically is taken in excess, which is oxidizing a known but a less quantity of hydrogen sulphide and the unreacted oxidant will oxidize furthero-tolidine to produce an orange yellow quinonediimine absorbing cation (λ max. 455 nm). Therefore, in principle, the decrease in color intensity of the absorbing system is proportional to the concentration of hydrogen sulphide. The stoichiometry between Mn(III) ando-tolidine and stability constant of the complex were determined by Job's continuous method, the corresponding values were found to be 2:1 and 1.42X105Lmol-1. The system was obeying Lambert-Beer's law in the range 0.2-1.4 μg mL-1of hydrogen sulphide. Molar absorptivity, correlation coefficient and Sandell's sensitivity values were also calculated and found to be 4.2062X103L mol-1cm-1, 0.999 and 0.0012 μg cm-2respectively. The method was employed for the determination of hydrogen sulphide in water samples. The results obtained were reproducible with acceptable standard deviation 0.01-0.068 and relative standard deviation, less than 3.21%. For a comparison, hydrogen sulphide present in water samples were also determined separately following the methylene blue official method. The results of the proposed method compare well with the official method.

Simultaneous determination of renal function biomarkers in urine using a validated paper-based microfluidic analytical device

“…The Fe 2þ -1,10-phenanthroline complex stoichiometry is 1:3 (metal:complexing agent), while the ratio between uric acid and Fe 3þ is not known. The latter was determined using Job's method (or method of continuous variation) [35]. The stoichiometric ratio was found to be 1 uric acid:2 Fe 3þ , which is the stoichiometry of the reaction.…”