🧂 Salt (NaCl) in food

Food Chemistry PN-ISO 1841-1

Determination of sodium chloride (NaCl) content in food by argentometric titration (Mohr or Volhard method). Key quality and safety parameter.

Overview

Determination of table salt (NaCl) content is one of the basic tests in food chemistry. Salt affects taste, stability, and safety of food products, and its excessive consumption is associated with cardiovascular disease risk. EU regulations (Reg. 1169/2011) require salt content declaration on labels.

Two main argentometric methods are Mohr method (direct titration) and Volhard method (back titration). In Mohr method, the sample is titrated with AgNO₃ solution in presence of K₂CrO₄ indicator — after binding all Cl⁻ ions, excess Ag⁺ reacts with CrO₄²⁻ forming red-brown Ag₂CrO₄ precipitate (endpoint). In Volhard method, excess AgNO₃ is back-titrated with KSCN with Fe³⁺ indicator (red FeSCN²⁺).

Standard PN-ISO 1841-1 describes Volhard method for meat and meat products. Volhard method is preferred for colored and turbid samples (meat, products) because the endpoint is easier to observe than in Mohr method. Before titration, the sample is mineralized or extracted with hot water, filtered, and acidified with nitric acid.

Alternative methods include: potentiometric chloride titration (more precise), chloride ion-selective electrodes (ISE), conductometric measurement, and sodium determination by AAS/ICP (calculation Na × 2.54 = NaCl). WHO recommends limiting salt intake to 5 g/day, making this determination important for public health.

Method principle

Volhard method (PN-ISO 1841-1): The sample is mineralized or extracted with hot water, filtered, and acidified with HNO₃. A measured excess of standardized AgNO₃ is added, which reacts with Cl⁻ ions forming white AgCl precipitate. Excess unreacted AgNO₃ is back-titrated with standardized KSCN (potassium thiocyanate) solution in presence of indicator — Fe³⁺ ions (ferric-ammonium alum solution). Endpoint is appearance of persistent red-brown coloration from FeSCN²⁺. Cl⁻ content is calculated from difference: n(Cl⁻) = n(AgNO₃ added) − n(KSCN consumed). NaCl [%] = Cl⁻ × 1.6485.

Applications

Key parameters

ParameterValue
Measurement range0.1–25% NaCl
Repeatability±0.05–0.1% NaCl
Sample size2–5 g
Titration pHpH < 2 (HNO₃ acidification)
Cl⁻ → NaCl conversion× 1.6485

Standard

Standard number
PN-ISO 1841-1:2002
Title (PL)
Mięso i przetwory mięsne — Oznaczanie zawartości chlorków — Część 1: Metoda Volharda
Title (EN)
Meat and meat products — Determination of chloride content — Part 1: Volhard method

Step-by-step procedure

1. Sample preparation

Homogenize sample. Weigh 2–5 g into conical flask with 0.001 g accuracy.

⏱ Time: 5 min

2. Chloride extraction

Add 100 mL hot distilled water. Boil for 15 min with stirring. Cool to room temperature.

⏱ Time: 30 min

3. Filtration

Filter through quantitative filter into 250 mL volumetric flask. Wash residue with hot water. Fill to mark.

⏱ Time: 15 min

4. Aliquot collection

Pipette 25–50 mL filtrate into 250 mL conical flask.

⏱ Time: 3 min

5. Acidification

Add 5 mL HNO₃ (1:1) — acidic environment required for Volhard method.

⏱ Time: 1 min

6. Excess AgNO₃ addition

Add measured volume (e.g., 25 mL) of standardized 0.1 mol/L AgNO₃ — excess relative to expected Cl⁻ content.

⏱ Time: 2 min

7. AgCl filtration (option)

Filter AgCl precipitate or add nitrobenzene to cover precipitate (prevent Ag⁺ readsorption on AgCl).

⏱ Time: 5 min

8. Indicator addition

Add 2 mL saturated ferric-ammonium alum solution (Fe³⁺ indicator).

⏱ Time: 1 min

9. KSCN titration

Titrate excess Ag⁺ with 0.1 mol/L KSCN solution to persistent red-brown coloration (FeSCN²⁺).

⏱ Time: 5–10 min

10. Calculations

Cl⁻ [mg] = (V_AgNO₃ × c_AgNO₃ − V_KSCN × c_KSCN) × 35.453. NaCl [%] = Cl⁻ × 1.6485 × 100 / sample mass.

11. Quality control

Perform duplicates. Analyze NaCl standard solution every series. Duplicate difference < 0.1% NaCl.

Required equipment and apparatus

EquipmentExampleIndicative price
Automatic burette 50 mLBrand Titrette, Hirschmann Solarus1 500–4 000 PLN
Potentiometric titrator (option)Metrohm 888 Titrando, Mettler Toledo T520 000–45 000 PLN
Analytical balance 0.1 mgMettler Toledo ME204, Radwag AS 220.R28 000–20 000 PLN
Hot plate with stirrerIKA C-MAG HS 7, Heidolph MR Hei-Tec2 000–5 000 PLN
Volumetric flasks 100–250 mLDURAN class A, with certificate, set of 6 pcs.200–400 PLN
Erlenmeyer flasks 250 mLDURAN / Simax, set of 10 pcs.100–250 PLN

Reagents, media and consumables

ReagentCASDetails
Silver nitrate AgNO₃ 0.1 mol/L7761-88-8Standardized solution, 1 L bottle with certificate. Protect from light.
Potassium thiocyanate KSCN 0.1 mol/L333-20-0Standardized solution for back titration of excess Ag⁺
Nitric acid HNO₃ diluted (1:1)7697-37-2For solution acidification before titration
Ferric-ammonium alum (indicator)7783-83-7Saturated NH₄Fe(SO₄)₂·12H₂O solution — Volhard indicator (Fe³⁺)
Potassium chromate K₂CrO₄ 5% (Mohr method)7789-00-6Mohr method indicator — yellow, endpoint brick-red Ag₂CrO₄
Nitrobenzene (optional)98-95-3To shield AgCl precipitate in Volhard method (preventing reverse reaction)

Health and safety (OHS)

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