⛽ Petroleum hydrocarbons in water

Physicochemistry PN-EN ISO 9377-2

Determination of mineral oil index (C₁₀–C₄₀) in water by solvent extraction, Florisil cleanup, and gas chromatography GC-FID.

Overview

The hydrocarbon oil index (HOI) is a key parameter for assessing water contamination with petroleum hydrocarbons. The ISO 9377-2 method measures the sum of non-polar hydrocarbons with chains from n-decane (C₁₀) to n-tetracontane (C₄₀), covering a wide range of petroleum substances: gasoline, diesel, lubricants, machine oils, fuel oil.

This standard is one of the most commonly used standards in environmental analysis in Europe. The HOI index is a mandatory parameter in monitoring wastewater from petroleum industry facilities, fuel stations, automotive workshops, ports, and in assessing groundwater contamination with petroleum substances.

The method includes extraction of hydrocarbons from water with organic solvent (n-pentane, n-hexane or their mixtures), cleanup of extract on Florisil (magnesium silicate adsorbent) to remove polar substances (fats, fatty acids, resins), and subsequent GC-FID chromatographic analysis.

Method principle

The method consists of three stages: (1) extraction, (2) Florisil cleanup, (3) GC-FID analysis.

1. Extraction: Water sample is extracted with hydrocarbon solvent (boiling range 36–69°C, e.g., n-pentane or n-hexane). Petroleum hydrocarbons pass into organic phase.

2. Florisil cleanup: Extract is passed through Florisil column (MgSiO₃, 150–250 µm, activated at 140°C/16h). Florisil retains polar compounds (fats, esters, acids), passing non-polar hydrocarbons.

3. GC-FID analysis: Cleaned extract is injected on capillary GC column with non-polar phase (e.g., DB-1 or HP-5). Flame ionization detector (FID) records signal proportional to mass of hydrocarbons burned in H₂/air flame. Total peak area is integrated between retention times of n-decane (C₁₀) and n-tetracontane (C₄₀).

HOI [mg/L] = (sample area − blank area) × calibration factor / sample volume

Applications

Key parameters

ParameterValue
Hydrocarbon rangeC₁₀ (n-decane) to C₄₀ (n-tetracontane)
Limit of quantification0.1 mg/L
Working range0.1–100+ mg/L (with dilution)
DetectorFID (Flame Ionization Detector)
GC columnCapillary, non-polar phase (DB-1, HP-5), 10–30 m
GC analysis time5–20 min (with oven cooling)

Standard

Standard number
PN-EN ISO 9377-2:2003
Title (PL)
Jakość wody — Oznaczanie indeksu oleju mineralnego — Część 2: Metoda z zastosowaniem ekstrakcji rozpuszczalnikiem i chromatografii gazowej
Title (EN)
Water quality — Determination of hydrocarbon oil index — Part 2: Method using solvent extraction and gas chromatography

Step-by-step procedure

1. Sample preparation

Collect sample in 1–2 L glass bottle (not PE/PP — adsorb hydrocarbons). Acidify with HCl to pH 2. Do not filter. Analysis within 7 days, store at 4°C.

⏱ Time: 5 min

2. Extraction

Transfer 1 L sample to 2 L separatory funnel. Add 30 mL n-pentane. Shake 5 min. Separate phases. Repeat 2× with 20 mL. Combine pentane extracts.

⏱ Time: 30 min

3. Florisil cleanup

Pass extract through column with 2 g Florisil (saturated with solvent). Elute with 20 mL solvent. Florisil retains polar contaminants.

⏱ Time: 15 min

4. Concentration (optional)

If concentration low: concentrate extract with N₂ stream to ~1 mL (T < 40°C). Do not evaporate to dryness (loss of volatile hydrocarbons!).

⏱ Time: 15–30 min • 🌡 Temperature: <40°C

5. GC-FID analysis

Inject 1–2 µL on capillary column. Temperature program: 40°C (1 min) → 10°C/min → 320°C (5 min). FID detector 350°C. Gases: H₂ 40 mL/min, air 400 mL/min.

⏱ Time: 30 min/sample • 🌡 Temperature: 40–320°C

6. Integration and calculations

Determine C₁₀–C₄₀ retention window based on n-alkane standards. Integrate total peak area in this window. Calculate HOI from calibration curve.

⏱ Time: 10 min

7. Quality control

Blank sample (dist. water through entire procedure). Control standard every 10 samples. CRM. Duplicate every 20 samples. Recovery from fortified sample 70–120%.

⏱ Time: 10 min

Required equipment and apparatus

EquipmentExampleIndicative price
Gas chromatograph with FIDAgilent 8890, Shimadzu GC-2030, Thermo TRACE 1310120 000–300 000 PLN
Capillary GC columnAgilent DB-1 / DB-5, Restek Rtx-1, 10–30 m × 0.25 mm × 0.25 µm1 500–3 000 PLN
AutosamplerAgilent 7693A, Shimadzu AOC-20i40 000–80 000 PLN
Extraction system2 L separatory funnels or automated liquid-liquid extraction system200–500 PLN (funnels) / 30 000–80 000 PLN (automated)
Florisil columnGlass column 10 mm × 200 mm, Florisil 150–250 µm (60–100 mesh)100–500 PLN (column) + 300–800 PLN/kg (Florisil)
Evaporator (optional)N₂ blowdown system or Kuderna-Danish for extract concentration3 000–15 000 PLN

Reagents, media and consumables

ReagentCASDetails
n-Pentane or n-hexane109-66-0 / 110-54-3Purity for hydrocarbon analysis (pesticides/GC grade). Extraction solvent, boiling range 36–69°C
Florisil1343-88-0150–250 µm (60–100 mesh). Activate at 140°C for 16h. For cleanup of extract from polar substances
n-Alkane standards (C₁₀, C₄₀)For determining retention window. n-Decane (C₁₀) and n-tetracontane (C₄₀) in solvent
HOI calibration standardMineral oil mixture (e.g., Type B per ISO 9377-2) in solvent, certified concentration
Anhydrous sodium sulfate (Na₂SO₄)7757-82-6Calcined (400°C, 4h). For drying organic phase
Hydrogen and synthetic airGases for FID detector. H₂ 5.0, synthetic air (hydrocarbon-free)

Health and safety (OHS)

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