0.1M Thiosulfate Standardization Against Potassium Iodate: Iodometric Titration
0.1M Thiosulfate Standardization Against Potassium Iodate: Iodometric Titration
This reaction needs presence of acid. As it was already signalled on the iodometric titration
overview page, low pH both helps air oxygen oxidize iodides to iodine and speeds up thiosulfate
decomposition. Both reactions are detrimental for the standardization, but they can be ignored if
the water is oxygen free and titration doesn't take too long.
Procedure to follow:
Weight exactly about 0.10-0.15g of dry potassium iodate and transfer it to Erlenmayer
flask.
Add 40 mL of freshly boiled distilled water
Enter potassium iodate mass in the upper (input) frame in the mass edit field above
KIO3 formula. Click n=CV button below thiosulfate in the output frame, enter volume
of the solution used, read solution concentration.
First reaction is not too fast, so after mixing reagents they should be left for 5 minutes. Also final
color is different from what we are usually seeing during iodometric titrations, as solution
contains trivalent, green chromium.
Procedure to follow:
Pour 80 mL of freshly boiled, distilled water into Erlenmayer flask (or better - flask with
glass stopper).
Titrate swirling the flask, until yellow iodine tint is barely visible.
This is a two step process, but iodine is only intermediate, and the stoichiometry of
the overall reaction that we are interested in is
This is not an exact reaction equation describing what is happening in the solution, but
it has correct stoichiometric coefficients and allows easy calculation of amount of
thiosulfate reacting with a given mass of potassium dichromate.
Enter potassium dichromate mass in the upper (input) frame in the mass edit field
above K2Cr2O7 formula. Click n=CV button below thiosulfate in the output frame,
enter volume of the solution used, read solution concentration.
If we have iodine solution of known concentration we can easily use it as a standard for
thiosulfate solution standardization and vice versa. This is a common situation in the lab practice.
The only problem is selection of the volume of thiosulfate sample. If we use 50 mL burette, and
both solutions are 0.1N (that means 0.05M solution of iodine and 0.1M solution of thiosulfate),
we should use 45 mL of thiosulfate - to make sure we use as large volume of the iodine solution
as possible to minimize effects of the volume reading error. However, there are no single volume
volumetric pipettes of 45 mL volume :) The most logical approach is to use 20 mL pipette and 25
mL burette.
Procedure to follow:
Titrate swirling the flask, until a blue color persists for 20 seconds.
Click n=CV button over thiosulfate. Enter concentration and volume of the sample,
click Use button. Click n=CV button below iodine in the output frame, enter volume
of the solution used, read solution concentration.
Again, we have a problem with selection of the volume of titrated sample, and again the most
logical approach is to use 20 mL pipette and 25 mL burette.
Procedure to follow is also very similar, just the moment of adding the indicator is different and
we titrate not till color appears, but till it disappears: