Determination of Water Content in Acetic acid Using Karl Fischer Titration

Product Group

Carboxylic acids

General Information concerning the product group

Carboxylic acids

Most carboxylic acids can be analysed relatively easily following standard KF titration methods. Due to their weakly acidic properties they exhibit only a slight effect on the pH of the KF solution. Only the stronger acids require neutralisation or buffering of the solvent prior to measuring. This is achieved by the use of organic amines. In some cases esterification with methanol results in the formation of water. This potential interference should especially be taken into account with coulometric determination. In the event of solubility problems solubilisers may be added. With some substances, only the adherent moisture can be determined by volumetric titration, or alternatively KF oven technology may be employed.

Special Information concerning the sample and the methods

In methanolic solutions a slow esterification of acetic acid takes place. Water determination can be carried out according to standard methods if the KF solvent is changed frequently and sample sizes are small.

Titration one component system

Reagents:

Titrant
188005 Aquastar^® - CombiTitrant 5 - One component reagent for volumetric Karl Fischer titration, 1 mL = approx. 5 mg water
or
188002 Aquastar^® - CombiTitrant 2 - One component reagent for volumetric Karl Fischer titration, 1 mL = approx. 2 mg water

Solvent
50 mL 188008 Aquastar^® - CombiSolvent - Methanol-free solvent for volumetric Karl Fischer titration with one component reagents
or
50 mL 188009 Aquastar^® - CombiMethanol - Solvent for volumetric Karl Fischer titration with one component reagents, max. 0.01 % water

Titration Parameters:
Default titration setttings, e.g.:
I(pol) = 20 - 50 µA, U(EP) = 100 - 250 mV
Stop criterion: drift < 20 µL/min

Sample size:
5 mL

Procedure:
The titration medium is first placed into the cell and titrated dry by means of the titrant. Then the sample is added with a syringe (exact sample weight determination by weighing of syringe before and after injection) or volumetric pipette and the titration is started. If cell drift rises strongly and titration time increases significantly, the KF solvent must be changed.

Titration two component system

Reagents:

Titrant
188010 Aquastar^® - Titrant 5 - Titrant for volumetric titration with two component reagents, 1 mL = approx. 5 mg water
or
188011 Aquastar^® - Titrant 2 - Titrant for volumetric titration with two component reagents, 1 mL = approx. 2 mg water

Solvent
50 mL 188015 Aquastar^® - Solvent - Solvent for volumetric titration with two component reagents

Titration Parameters:
Default titration settings, e.g.:
I(pol) = 20 - 50 µA, U(EP) = 100 - 250 mV
Stop criterion: drift < 20 µL/min

Sample size:
5 mL

Procedure:
The titration medium is first placed into the cell and titrated dry by means of the titrant. Then the sample is added with a syringe (exact sample weight determination by weighing of syringe before and after injection) or volumetric pipette and the titration is started. If cell drift rises strongly and titration time increases significantly, the KF solvent must be changed.

Coulometry with diaphragm

Reagents:

Catholyte
5 mL 109255 Aquastar^® - CombiCoulomat frit - Coulometric Karl Fischer reagent for cells with diaphragm

Anolyte
100 mL 109255 Aquastar^® - CombiCoulomat frit - Coulometric Karl Fischer reagent for cells with diaphragm

Titration Parameters:
Default coulometer settings for cell with diaphragm:
For end point indication, e.g.:
I(pol) = 5 - 10 µA, U(EP) = 50 - 100 mV
Stop criterion for fast titration: drift < 15 µg/min

Sample size:
0.5 - 1 mL

Procedure:
The Karl-Fischer reagent is placed into the cathode and anode compartment of the titration cell with diaphragm. The coulometer is started and the solvent is titrated dry. After preliminary titration and stabilisation of drift the sample is injected into the titration cell with a syringe (exact sample weight determination by weighing of syringe before and after injection) and the water determination is started. Titration is carried out to fast end point. It is possible to analyse approximately 8 g of acetic acid before the KF solvent needs to be changed.

Coulometry without diaphragm

Reagents:

Working medium
100 mL 109257 Aquastar^® - CombiCoulomat fritless - Coulometric Karl Fischer reagent for cells with or without diaphragm

Titration Parameters:
Default coulometer settings for cell without diaphragm:
For end point indication, e.g.:
I(pol) = 5 - 10 µA, U(EP) = 50 - 100 mV
Stop criterion for fast titration: drift < 15 µg/min

Sample size:
0.5 - 1 mL

Procedure:
The Karl-Fischer reagent is placed into the titration cell without diaphragm. The coulometer is started and the solvent is titrated dry. After preliminary titration and stabilisation of drift the sample is injected into the titration cell with a syringe (exact sample weight determination by weighing of syringe before and after injection) and the water determination is started. Titration is carried out to fast end point. It is possible to analyse approximately 8 g of acetic acid before the KF solvent needs to be changed.