Abstract
SnII in the plating solutions can usually be titrated by iodin method. SnIV therefore, must be reduced to SnII for the titration. This reduction, however, is rather difficult and might cause some error due to the oxidation by air during the course of analysis.
So, the author tried to develop a method to avoid such an error as follows:
First, SnII was titrated directly in the EDTA standard solution, masking SnIV with NH4F, keeping pH at 5.5-6.0, with pyridine-acetic acid as buffer solution and using methyltymol blue as indicator.
Next, to analyse SnII+SnIV, another portion of the solution was made acidic with HCl., to which an excess amount of EDTA standard solution was added and boild for a few minutes. Keeping the pH value of the solution between 2.5 and 3.5 with CH3COONH4 using dinitrophenol as pH indicator, it was then back titrated with ThIV standard solution with xylenol orange as indicator.
Figures obtained by this process descrived above were coincident with those given by iodin method for SnII and by gravity method for SnIV+SnII.