6.8.3 WS KF Moist

Section 8: Refined sugar p 1/4

Method 8.3 – Refined sugar:

moisture by Karl Fischer titration
1. Rationale

This method is applicable to refined sugar and speciality sugars and determines the total
moisture content of the sample.
2. Principle
The moisture in sugar is present in three forms:
§ free moisture contained on the surface of the crystal leaving the centrifugals,
which is easily and quickly removed on drying,
§ bound moisture contained in the glassy layer on the surface and in the re -entrant
angles, and which is released slowly as the glass crystallizes, and
§ inherent moisture included within the crystal structure and released only, in
general, by grinding.
This method determines the total moisture electrochemically by titrating with two Karl
Fischer reagents in the presence of a double platinum electrode to which a constant DC
voltage is applied. The first reagent is Hydranal-Composite 5 which consists of iodine,
sulphur dioxide and imidazole dissolved in diethylene glycol monoethyl ethter (DEGEE).
The second acts as the solvent and is a mixture of formamide and methanol. In the
presence of water, the sulphur dioxide is oxidised by the iodine to sulphuric acid, in
accordance with the following equation.
SO2 + I 2 + 2H2 O → 2HI + H2 SO4
The reaction is irreversible due to the presence of the formamide. When no more water is
left in the reaction mixture, the free iodine acts as a depolariser to cause a measurable
change in the electrode voltage.
3. Apparatus
3.1 Karl Fischer titrating apparatus
3.2 Micro-syringe: 25 µl
3.3 Self-indicating silica gel in a glass tube with cotton wool
3.4 Sample tube
The tube should be 82 mm long and 23 mm φ with a rubber stopper through

which there is fitted a thin long glass tube with a stopper. The capacity is such
that the tube will hold a sample of 20 - 30 g.
3.5 Analytical balance readable to 0.0001 g
Revised July 2005 SASTA Method 8.3: KF moisture

4. Reagents
4.1 Hydranal-Composite 5 (Karl Fisher titrant)
The Hydranal-Composite 5 titrant is harmful to human health. Wear gloves and safety
glasses during use.
4.2 Formamide
Formamide is a flammable solvent, is toxic and corrosive to the eyes and respiratory tract.
Only open in a fume cupboard while wearing gloves and safety glasses.
4.3 Methanol
Methanol is a flammable solvent and is toxic to humans. Wear safety glasses to avoid
contact with the eyes.
4.4 Formamide:Methanol solvent
Prepare a sufficient quantity of a 1:1 mixture of formamide and methanol. This mixture is
also available commercially.
4.5 Distilled water
5. Procedure
5.1 Drying of the reaction jar
Introduce 60 cm 3 of formamide:methanol mixture to the jar and titrate to dryness. The

solution must be stirred at a constant rate. This reading is determined when the pulse,
which changes because of the reaction, lies between 90-100%. Stop the stirrer and swirl
the jar to make sure that all the drops of formamide:methanol mixture on the sides of the
jar are mixed into the bulk of the solution. Start the stirrer and titrate once again to
dryness. Repeat this until the jar is completely dry.
5.2 Standardisation of the Karl Fischer titrant
Fill a 25 µl syringe with distilled water and record the mass. Introduce approximately
0.025 g of distilled water into the reaction jar and reweigh the syringe. The difference in
weight is recorded. Titrate to dryness and record the volume of Karl Fischer titrant used.
Repeat with another portion of water. Calculate the water equivalent as indicated in 6.1.
The duplicate determinations of the water equivalent should agree to within 0.05 units.
The formamide:methanol solvent should not be used more than twice for the
determination of the water equivalent
5.3 Blank
Open the dry reaction jar for 25 seconds, close and stir for 30 minutes to simulate the
introduction and dissolution of a sample. Clear the volume reading. Titrate to dryness
and record the volume of the titrant used. This is the blank volume.
5.4 Analysis
Introduce 60 cm 3 of fresh formamide:methanol solvent to the reaction jar and dry

according to the procedure indicated in 5.1. Weigh the sample tube containing the sugar
to 0.001 g. Introduce the sugar to the jar (± 5 g), close and stir for 30 minutes. Reweigh
the empty tube and record the mass. Clear the volume reading. Titrate to dryness, record

the volume of titrant used and empty the jar. For subsequent samples only do steps 5.1
and 5.4.
6. Calculations
6.1 Standardisation of the Karl Fischer Titrant (water equivalent)
mass of water = M1 - M2
where M1 ≡ mass of syringe before addition (g)

M2 ≡ mass of syringe after addition (g)
mass of water (g) × 1000

water equivalent (mg/cm 3 ) =
volume of reagent (cm 3 )
6.2 Moisture in sample
mass of sugar = M3 - M4
where M3 ≡ mass of tube before sample introduction (g)

M4 ≡ mass of tube after sample introduction (g)
corrected titre (cm 3 ) = volume KF titrant (cm 3 ) - blank volume (cm 3 )
titre (cm 3 ) × water equivalent (factor, mg/cm3 )

moisture % sample = × 100
mass of sample (g) × 1000
Report results in percentage to 3 decimal places.
7. Example
7.1 Determination of the water equivalent (factor)
mass of syringe before addition = 12.5031 g

mass of syringe after addition = 12.4786 g
mass of water = (12.5031 - 12.4786) g
= 0.0245 g
titre of Karl Fischer titrant = 5.64 cm 3
0.0245 g × 1000
water equivalent (factor) =
5.64 cm 3
= 4.344 mg/cm 3
Repeat
mass of syringe before addition = 12.5012 g

mass of syringe after addition = 12.4785 g
mass of water = (12.5012 - 12.4785) g

= 0.0227 g

0.0227 g × 1000
water equivalent (factor) =
5.27 cm 3
= 4.307 mg/cm 3
average of the two factors =

(4.344 + 4.307 ) mg/cm3
2
= 4.326 mg/cm 3
blank volume = 0.21 cm 3
7.2 Determination of the sample moisture
mass of tube before sample introduction = 51.5512 g

mass of tube after sample introduction = 31.9704 g
mass of sugar = 19.5808 g

corrected titre = (1.42 - 0.21) cm 3
= 1.21 cm 3
1.21 cm 3 × 4.326 mg/cm3

moisture in sample = × 100
19.5808 g × 1000
= 0.027%
8. Precision
The tolerance associated with the analysis is ± 0.005 unit.
9. References
ICUMSA (1994). Moisture in speciality sugars, molasses, cane raw sugars and syrups by
the Karl Fischer procedure. ICUMSA Methods Book, GS4/7/3-12.
SMRI (2000). Determination of the moisture in white sugar using Karl Fischer ti tration
method. SMRI Test Methods, TM031.

6.8.3 WS KF Moist

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Section 8: Refined sugar p 1/4

Method 8.3 – Refined sugar:

The moisture in sugar is present in three forms:

SO2 + I 2 + 2H2 O → 2HI + H2 SO4

3.1 Karl Fischer titrating apparatus

3.3 Self-indicating silica gel in a glass tube with cotton wool

3.4 Sample tube

The tube should be 82 mm long and 23 mm φ with a rubber stopper through

3.5 Analytical balance readable to 0.0001 g

Revised July 2005 SASTA Method 8.3: KF moisture

4.4 Formamide:Methanol solvent

4.5 Distilled water

5.1 Drying of the reaction jar

Introduce 60 cm 3 of formamide:methanol mixture to the jar and titrate to dryness. The

5.2 Standardisation of the Karl Fischer titrant

Introduce 60 cm 3 of fresh formamide:methanol solvent to the reaction jar and dry

Revised July 2005 SASTA Method 8.3: KF moisture

6.1 Standardisation of the Karl Fischer Titrant (water equivalent)

where M1 ≡ mass of syringe before addition (g)

mass of water (g) × 1000

6.2 Moisture in sample

where M3 ≡ mass of tube before sample introduction (g)

corrected titre (cm 3 ) = volume KF titrant (cm 3 ) - blank volume (cm 3 )

titre (cm 3 ) × water equivalent (factor, mg/cm3 )

Report results in percentage to 3 decimal places.

7.1 Determination of the water equivalent (factor)

mass of syringe before addition = 12.5031 g

titre of Karl Fischer titrant = 5.64 cm 3

mass of syringe before addition = 12.5012 g

mass of water = (12.5012 - 12.4785) g

titre of Karl Fischer titrant = 5.27 cm 3

Revised July 2005 SASTA Method 8.3: KF moisture

average of the two factors =

blank volume = 0.21 cm 3

7.2 Determination of the sample moisture

mass of tube before sample introduction = 51.5512 g

titre of Karl Fischer titrant = 1.42 cm 3

1.21 cm 3 × 4.326 mg/cm3

The tolerance associated with the analysis is ± 0.005 unit.

Revised July 2005 SASTA Method 8.3: KF moisture

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