💧 Moisture — general Karl Fischer method

Physicochemistry PN-EN ISO 760

Determination of water content in chemical, pharmaceutical, cosmetic and petrochemical samples by Karl Fischer titration (volumetric or coulometric).

Overview

The Karl Fischer (KF) method is the most common and most selective technique for determining water content in a wide range of materials — from organic solvents and oils, through pharmaceutical and cosmetic products, to food, polymers and building materials. The method developed in 1935 by German chemist Karl Fischer uses selective reaction of water with iodine in presence of sulfur dioxide and base in methanol medium.

Standard PN-EN ISO 760 describes the general Karl Fischer method in volumetric variant — used for samples with water content from 100 ppm to 100%. Coulometric variant (electrochemical iodine generation) is used for samples with very low water content — below 50–100 ppm (0.005–0.01%).

The key advantage of KF method is its selectivity — it reacts only with water, not with other volatile components. It is an absolute (stoichiometric) method, requiring only periodic verification of reagent titer. Modern KF titrators are fully automatic — with reagent dosing, bipotentiometric endpoint detection and calculations.

Analytical laboratories use KF method routinely: pharmaceuticals (quality control of raw materials and drugs), petrochemicals (water determination in oils, fuels, solvents), cosmetics, chemical industry, environmental laboratories (soil moisture, sediments).

Method principle

Karl Fischer reaction: H₂O + I₂ + SO₂ + 3 Base + CH₃OH → [Base·H]⁺·SO₄CH₃⁻ + 2[Base·H]⁺·I⁻. Water reacts stoichiometrically with iodine (1 mol H₂O = 1 mol I₂). In volumetric variant, KF reagent (containing iodine) is dosed from burette into sample dissolved in methanol. Endpoint — moment when small excess iodine persists in solution — is detected bipotentiometrically (double platinum electrode). In coulometric variant, iodine is generated electrochemically in situ from iodide in solution — electric charge is proportional to water amount (Faraday's laws).

Applications

Key parameters

ParameterValue
Volumetric range100 ppm – 100% H₂O
Coulometric range1 ppm – 5% H₂O
Accuracy±0.1–0.3% (volumetric), ±3 µg H₂O (coulometric)
Sample volume (volumetric)0.1–10 mL or 10–500 mg (solids)
Determination time2–10 min/sample
Working temperature20–25°C (titration cell)

Standard

Standard number
PN-EN ISO 760:2018
Title (PL)
Oznaczanie zawartości wody — Metoda Karla Fischera (metoda ogólna)
Title (EN)
Determination of water — Karl Fischer method (General method)

Step-by-step procedure

1. Titrator preparation

Turn on titrator, check reagent levels. Fill cell with working solvent (Hydranal Medium K). Run pre-titration to remove residual moisture.

⏱ Time: 10 min

2. Titer verification

Inject 10–20 µL water standard (Hydranal Water Standard 10.0). Titrate. Check agreement with certified value ±3%.

⏱ Time: 5 min

3. Sample preparation

Liquid samples — draw with syringe, weigh. Solid samples — weigh 50–500 mg, introduce through opening. Hard-to-dissolve samples — use KF oven (120–250°C).

⏱ Time: 5 min

4. Sample introduction to cell

Inject liquid sample through septum or introduce solid through opening. Titrator automatically starts titration.

⏱ Time: 1 min

5. Titration

Titrator doses Hydranal Composite 5 (volumetric) or generates iodine (coulometric). Magnetic stirring. Bipotentiometric detection.

⏱ Time: 2–10 min

6. Result reading

Titrator automatically calculates water content: % wt. or ppm (mg/kg). Record result with sample identification.

⏱ Time: 1 min

7. Duplicate

Repeat determination at least 2 times. Difference between duplicates: ≤10% relative value for low concentrations, ≤2% for high.

⏱ Time: 5–15 min

8. Quality control

Every 10 samples verify titer with standard. Per series determine blank (drift correction). Maintain control chart.

⏱ Time: 5 min

9. Cleaning and maintenance

After work empty cell, rinse with methanol. Replace septum. Seal openings. Replace molecular sieves in reagent bottle.

⏱ Time: 10 min

Required equipment and apparatus

EquipmentExampleIndicative price
Volumetric KF titratorMetrohm 888 Titrando, Mettler Toledo V30S, Hanna HI93420 000–60 000 PLN
KF coulometerMetrohm 917 Coulometer, Mettler Toledo C30S25 000–70 000 PLN
Evaporation oven (KF Oven)Metrohm 860 KF Thermoprep, Mettler Toledo DO30830 000–80 000 PLN
Double platinum electrodeMetrohm 6.0338.100, Mettler Toledo DM143-SC500–1 500 PLN
Analytical balance 0.01 mgMettler Toledo XPR205, Sartorius Cubis II15 000–50 000 PLN
Dosing syringes (liquid samples)Hamilton, 1–10 mL, with Luer Lock connection200–800 PLN

Reagents, media and consumables

ReagentCASDetails
Hydranal Composite 5 (volumetric titrant)Honeywell/Fluka, one-component, methanol-free, 1 mL = ~5 mg H₂O, 500 mL bottle
Hydranal Medium K (working solvent)Honeywell/Fluka, medium for volumetric titration cell, 1 L bottle
Hydranal Coulomat AG (coulometric anolyte)Honeywell/Fluka, anode solution for coulometer with diaphragm, 500 mL bottle
Hydranal Coulomat CG (catholyte)Honeywell/Fluka, cathode solution for coulometer with diaphragm, 500 mL bottle
Water standard (Water Standard)7732-18-5Hydranal Water Standard 10.0 (10.0 mg H₂O/g), certified CRM for titer verification
Anhydrous methanol pure67-56-1For cell cleaning and as alternative solvent, H₂O content <0.01%, 1 L
Iodine (reagent component)7553-56-2Active component of KF reagent, stoichiometric reaction with H₂O (1:1 mol)
Sulfur dioxide (reagent component)7446-09-5SO₂ in KF solution, participates in Bunsen-Fischer reaction

Health and safety (OHS)

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