⚗️ Sulfates in Water

Physicochemistry PN-ISO 9280

Gravimetric determination of sulfates (SO₄²⁻) in water by barium chloride precipitation method. Classical, reference gravimetric method with high accuracy.

Overview

Sulfates (SO₄²⁻) are one of the main anions occurring in natural waters. They originate from: mineral dissolution (gypsum CaSO₄, anhydrite), sulfide oxidation (pyrite FeS₂), atmospheric precipitation (acid rain — SO₂→H₂SO₄), industrial wastewater (pulp and paper, mining, galvanizing), and agriculture (sulfur fertilizers).

Drinking water standard: ≤250 mg SO₄²⁻/L (Polish Ministry of Health Regulation) — higher concentrations cause bitter taste and laxative effects. At high concentrations sulfates intensify concrete and metal installation corrosion (sulfate corrosion).

Gravimetric ISO 9280 method is reference (most accurate) method for sulfate determination. It involves BaSO₄ precipitation, filtration, ignition, and precipitate weighing. It is time-consuming but indispensable for arbitration and rapid method validation (turbidimetric).

Method principle

Sulfate ions in acidified sample (HCl) react with barium chloride (BaCl₂) forming white, crystalline, practically insoluble barium sulfate precipitate:

SO₄²⁻ + Ba²⁺ → BaSO₄↓ (white)

BaSO₄ precipitate is filtered through ashless filter paper or filter crucible, washed with hot water (removing Cl⁻ and Ba²⁺ ions), dried and ignited in muffle furnace at 800°C to constant mass.

SO₄²⁻ [mg/L] = (m_BaSO₄ × 0.4116 × 1000) / V_sample

where 0.4116 = conversion factor (M_SO₄/M_BaSO₄ = 96.06/233.39). Sample is acidified with HCl and boiled to ensure slow precipitation and obtain large, well-filtering crystals (minimizing coprecipitation).

Applications

Key parameters

ParameterValue
Measurement range≥10 mg SO₄²⁻/L
Accuracy±1–2% (at concentration >50 mg/L)
Ignition temperature800 ± 25°C
Weighing accuracy0.1 mg (analytical balance)
Analysis time8–12 hours (with ignition and cooling)
MethodPrecipitation gravimetry (reference)

Standard

Standard number
PN-ISO 9280:2002
Title (PL)
Jakość wody -- Oznaczanie siarczanów(VI) -- Metoda grawimetryczna z chlorkiem baru
Title (EN)
Water quality — Determination of sulfate — Gravimetric method using barium chloride

Step-by-step procedure

1. Sample preparation

Measure 200–500 mL sample (select volume for expected concentration, so BaSO₄ mass is 50–300 mg). Filter through 0.45 μm filter if sample turbid.

⏱ Time: 10 min

2. Acidification

Add HCl (1+1) to pH ~1–2 (indicator paper or pH meter). Typically 5–10 mL HCl per 200 mL sample. Acidification prevents BaCO₃ coprecipitation.

⏱ Time: 2 min

3. Boiling and precipitation

Bring sample to boil on hot plate. To boiling sample add SLOWLY (dropwise) hot BaCl₂ solution (10%), mixing constantly. Add excess (~2 mL over calculated). Boil 15–30 minutes.

⏱ Time: 30 min • 🌡 Temperature: 100°C

4. Precipitate aging

Leave solution with precipitate on hot plate (80–90°C) for 2–4 hours or in warm place overnight. Aging improves precipitate crystallinity (Ostwald ripening).

⏱ Time: 2–12 h • 🌡 Temperature: 80–90°C

5. Filtration

Filter through ashless filter paper (Whatman 42) or filter crucible G4. Do not transfer entire precipitate — leave it in beaker as long as possible.

⏱ Time: 30 min

6. Precipitate washing

Wash precipitate with hot deionized water (min. 6 portions of 10 mL each). After each wash check filtrate for Cl⁻ presence (1 drop AgNO₃ — no turbidity = Cl⁻ washed out).

⏱ Time: 20 min

7. Drying and ignition

Ashless filter: place in porcelain crucible, dry at 105°C, ash carefully on burner, ignite in muffle furnace 800°C/1h. Filter crucible: dry 105°C, ignite 800°C/1h.

⏱ Time: 3 h • 🌡 Temperature: 800°C

8. Cooling and weighing

Cool crucible in desiccator to room temperature (min. 30 min). Weigh on analytical balance (0.1 mg). Repeat ignition and weighing to constant mass (difference <0.5 mg).

⏱ Time: 45 min

9. Calculations

SO₄²⁻ [mg/L] = (m_BaSO₄ × 0.4116 × 1000) / V_sample [mL]. Account for blank (titration of water alone with reagents).

10. Quality control

Blank: precipitate mass <0.5 mg. Duplicate: RPD <3%. Na₂SO₄ control standard — deviation max ±2%. Check precipitation completeness (add drop of BaCl₂ to filtrate — no turbidity).

Required equipment and apparatus

EquipmentExampleIndicative price
Analytical balance (0.1 mg)Mettler Toledo ME204, Sartorius Entris II, Radwag AS 220.R25 000–15 000 PLN
Muffle furnace (800°C)Nabertherm L 3/11, Snol 8.2/1100, POL-EKO SLF8 000–25 000 PLN
Laboratory dryer (105°C)Binder FD 115, Memmert UF1105 000–15 000 PLN
DesiccatorGlass with silica gel, ø 200–250 mm300–800 PLN
Filtration setPorous filter crucible (G4) or Whatman 42 ashless filters200–500 PLN
Hot plateFor boiling sample with BaCl₂, temperature control1 000–3 000 PLN
Glass beakers 400–600 mLDURAN borosilicate, wide, for precipitation25–60 PLN/pc

Reagents, media and consumables

ReagentCASDetails
Barium chloride BaCl₂·2H₂O10326-27-9Precipitating solution: 100 g/L (10%). Add hot to hot sample. WARNING: barium salts are toxic!
Hydrochloric acid HCl7647-01-0Diluted HCl (1+1) for sample acidification (pH ~1–2). Prevents carbonate coprecipitation.
Silver nitrate AgNO₃ (for test)7761-88-8Solution 0.1 mol/L — for checking wash completeness (absence of Cl⁻ in filtrate).
Ashless filter papersWhatman 42 or equivalent — ash <0.01%. For BaSO₄ precipitate filtration.
Deionized waterHot — for washing precipitate on filter (min. 6× 10 mL each).

Health and safety (OHS)

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