Analysis of Hypochlorite in Commercial Bleach:

Iodometric Titrimetry

Introduction

The oxidizing power (percent NaOCl) of commercial bleach is determined iodometrically

by reacting it with an excess of iodide in acetic acid solution and titrating the triiodide ion
produced ( is formed in the presence of excess iodide) with standard sodium
thiosulfate solution. The sodium thiosulfate is standardized against primary standard
potassium iodate, and a starch indicator is used for the endpoint detection.

Equations that govern the complex equilibrium of this iodometric titration:

Standardization of Na2S2O3:

In the reaction six thiosulfate ions (S2O32-) react for every iodate (IO3-) ion reacted.

Why do we call this an oxidation/reduction reaction?

The thiosulfate is oxidized and the iodate is reduced.

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DETERMINATION OF A HYPOCHLORITE SAMPLE
I3- is generated using ClO - in a 1 to 1 mole ratio and is then reacted with the standardized
thiosulfate solution. The following two reactions govern the iodometric titration of
hypochlorite:

In the reaction two thiosulfate ions (S 2O32-) react for every hypochlorite (ClO -) ion
reacted. The thiosulfate is oxidized and the hypochlorite is reduced.

Solutions needed for this experiment:

Solutions prepared by the student: Solutions provided by the instructor:

0.01 M KIO3 standard Glacial acetic acid
0.1 M Na2S2O3 Reagent sulfuric acid
6 M HCl Reagent hydrochloric acid
1 M H2SO4 Starch solution

Experimental Procedure:

Preparation of KIO3:

• Dry about 1.5 g of the primary standard KIO 3 at 120°C for 1-2 hours and cool in a
desiccator for 30-40 minutes.

• Accurately weigh out (to the nearest 0.0001g) 1.0 to 1.4 g of the salt (by difference) and
dissolve in a small amount of distilled water in a 200 ml beaker.

• Quantitatively transfer, with rinsing to a 500 ml volumetric flask using a glass funnel
ensuring all solution and any solid are transferred to the flask.

• Dilute to the mark.

• Calculate the molarity of the solution.

Preparation of 0.1M Na2S2O3:

• Boil about 700 ml of distilled water for 5-10 minutes to ensure sterility and to expel
carbon dioxide. (Sodium thiosulfate solutions are subject to bacterial attack, which may
change the molarity after some time. Therefore, all water and glassware used to prepare
and store the solution should be sterilized. If any turbidity or bacteria or mold growth
appears, the solution should be discarded. Removal of carbon dioxide is also beneficial,
because thiosulfate is more stable in neutral solution.)

2
• Cool to room temperature.

• Sterilize a 1-liter bottle with concentrated H2SO4; rotate the bottle so that the acid
contacts the entire interior wall. Caution! Highly Corrosive! Use the minimum
amount necessary.

• Rinse very thoroughly with tap water, then with distilled water, and finally with the
boiled distilled water.

• Using a rough balance (i.e., a top-loader), weigh out on weighing paper or weighing
boat 12.5 g of sodium thiosulfate crystals, Na2S2O3•5H2O.

• Transfer to the liter bottle, add about 500 mL of the freshly boiled and cooled distilled
water, add 0.05 g sodium carbonate, and shake thoroughly until the solution is
homogenous. (A small amount of sodium carbonate is added to keep the solution neutral
or slightly alkaline and thereby stabilize it against decomposition to elemental sulfur.)

• Store this solution in a dark, cool place (your locker).

Standardization of the Na2S2O3 solution. READ THIS PROCEDURE BEFORE

STARTING!! TIME DEPENDENT!!!!

1. Rinse the 50 ml burette several times with small portions of the thiosulfate solution
and fill it with thiosulfate solution. Adjust the volume near the zero mark and record
the volume reading to the nearest 0.01 ml. Pipette a 50.00 ml aliquot of the
potassium iodate solution into a clean 250 ml Erlenmeyer flask. Add about 2 g of
solid potassium iodide and swirl to dissolve. Add, with thorough, rapid mixing, 5 ml
of 1 M H2SO4. Once you have added the acid, you must be prepared to titrate!!

2. Titrate immediately with the thiosulfate solution. In strongly acidic solutions the
excess iodide is rapidly air-oxidized to I3-. Therefore, the titration must be performed
quickly without long delay times. Thorough, continuous mixing by swirling the flask
is required throughout the titration with the addition of each aliquot. The thiosulfate
must not be allowed to accumulate in local excess in the acid solution or else some
decomposition into H2SO3 and S may occur. Titrate until the yellow color (due to I3-)
almost disappears. The solution will become pale yellow. To ensure that you see this
place a white sheet of paper under the titration vessel. Once you observe the pale
yellow color add 2 to 3 ml of the starch indicator to the vessel and titrate until the
blue color just disappears. This should occur within the addition of the first 0.5 ml of
sodium thiosulfate after the starch indicator addition. If the solution does not turn
blue then you have over titrated your first trial and you should discard it and try
again.

3. Titrate two more 50.00 mL aliquots of potassium iodate. Calculate the molarity of
the Na2S2O3 solution based on your trials. Provide the mean, standard deviation, and
relative standard deviation.

Determination of Hypochlorite in an Unknown.

Bleach solutions are inherently unstable with storage, so do not prepare your
bleach solution unless you are prepared to titrate it the exact same lab period.
When you are ready to prepare and titrate the bleach solution, get an unknown
from your instructor.

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1. Wash and thoroughly dry a weighing bottle. Using the analytical balance, weigh the
empty weighing bottle to the nearest 0.0001 gram. The hypochlorite (bleach) solution
to be analyzed will be supplied by the instructor. Pipette 10.00 mL of the bleach
solution into the weighing bottle; it is essential that the upper portion of the bottle,
particularly the ground glass rim remain dry. Replace the stopper and weigh to the
nearest 0.0001 gram.

2. Empty the weighing bottle into a 250 ml volumetric flask containing about 100 ml of
water using a funnel. Wash out the weighing bottle and the funnel with water from
your wash bottle, catching the rinse in the volumetric flask. Dilute to the mark and
mix thoroughly. From this point on, handle each sample individually throughout the
remainder of the procedure.

3. Fill your burette with the standardized 0.1 M sodium thiosulfate solution. Measure
out and have ready 10 ml of glacial acetic acid and 2 g of potassium iodide. When
ready to titrate, pipette a 50.00 mL aliquot of the diluted bleach solution in a clean
250 mL Erlenmeyer flask containing about 50 mL of water. Rinse down the walls of
the flask in such a way as to form a layer of water above the sample. Add the acid to
the sample, mix, add the potassium iodide, and titrate immediately, swirling the flask
constantly. When the color has faded to a pale yellow, add 2 ml of starch solution
and then continue to titrate drop by drop until the solution becomes colorless. Titrate
two additional 50.00 mL aliquots the same way.

4. Calculate the percentage by weight of NaOCl in the solution. Note: Fresh

commercial bleach should contain at least 5% NaOCl. If less than 5%, it cannot
legally be called bleach. Nevertheless, the bleach sample used in class may contain
less than this. Report the mean, standard deviation, and relative standard deviation
for your analysis.

Report

Report the percent NaOCl in the unknown. Show all calculations and propagation of
error for one sample from start to finish. Calculate the mean, standard deviation, and
relative standard deviation for at least three samples. If you have questions regarding any
of the calculations required, please see the instructor.

4
SAMPLE REPORT

Analysis of Hypochlorite in Commercial Bleach:

Iodometric Titrimetry
Ben Affleck
Unknown # 

Standardization of Sodium Thiosulfate:

1st 2nd 3rd

M, KIO3 0.01009 0.01009 0.01009
mL KIO3 50.00 50.00 50.00
Initial buret mL 0.05 0.23 1.01
Final buret mL 30.02 30.15 30.89
mL, S2O3-2 29.97 29.92 29.88
mmoles, KIO3 0.5045 0.5045 0.5045
mmoles, S2O3-2 3.027 3.027 3.027
M, S2O3-2 0.1010 0.1012 0.1013
Mean S2O3-2 0.1012
Sx 0.0002
RSD 0.2%

Sample calcs for standardization:

1. mmoles KIO3 = mL KIO3 X M, KIO3

0.5045 mmoles = 50.00 mL x 0.01009 M

2. mmoles S2O3-2 = mmoles KIO3 X (6 S2O3-2 /1 KIO3 )

3.027 mmoles S2O3-2 = 0.5045 mmoles KIO3 X (6 S2O3-2 /1 KIO3 )

3. M, S2O3-2 = mmoles, S2O3-2 / Volume, S2O3-2

0.1010M = 3.027 mmoles S2O3-2 /29.97 mL S2O3-2

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Titration of Bleach:

Mass of undiluted bleach solution used: 10.8035 g

1st 2nd 3rd

mL diluted bleach solution 50.00 50.00 50.00
Initial buret mL 0.05 0.23 1.01
Final buret mL 29.02 29.15 29.89
mL, S2O3-2 28.97 28.92 28.88
M, S2O3-2 0.1012 0.1012 0.1012
mmoles S2O3-2 2.932 2.927 2.923
mmoles ClO- 1.466 1.463 1.461
mmoles ClO- in undiluted bleach 7.329 7.317 7.307
Mass NaOCl in undiluted bleach 0.5456 g 0.5447 g 0.5439 g
% NaOCl 5.050 5.042 5.034
Avg % NaOCl 5.042
Sx 0.008
RSD 0.2%

Sample calculations:

1. mmoles S2O3-2 = mL, S2O3-2 X M, S2O3-2

2.932 mmoles S2O3-2 = 28.97 mL, S2O3-2 X 0.1012 M, S2O3-2

2. mmoles ClO- = mmoles S2O3-2 X (1 ClO- /2 S2O3-2 )

1.466 mmoles ClO- = 2.932 mmoles S2O3-2 X (1 ClO- /2 S2O3-2 )

3. mmoles ClO- in undiluted bleach = mmoles ClO- X (250.00 mL diluted bleach

/ 50.00 mL aliquot)

7.329 mmoles ClO- in undiluted bleach = 1.466 mmoles ClO- X (250.00/50.00)

4. Mass NaOCl in undiluted bleach = 7.329 mmoles ClO- in undiluted bleach X

(FW NaOCl/1000)

0.5456 g NaOCl in undiluted bleach = 7.329 mmoles ClO- in undiluted bleach

X (74.44/1000)