⛽ Hydrocarbon Oil Index in Water — Petroleum Hydrocarbons (GC-FID)

Physicochemistry PN-EN ISO 9377-2

In short

Determination of mineral oil index (C₁₀–C₄₀) in water by solvent extraction, Florisil cleanup, and gas chromatography GC-FID. The test is performed according to PN-EN ISO 9377-2:2003; Hydrocarbon range: C₁₀ (n-decane) to C₄₀ (n-tetracontane). The procedure comprises 8 steps (about 2 h 5 min–2 h 20 min in total); it is used for: Monitoring of wastewater from refineries and petrochemical plants, Control of groundwater (fuel contamination from leaking tanks), Study of surface waters (oil spill, ecological disasters).

At a glance

  • Standard: PN-EN ISO 9377-2:2003
  • Category: Physicochemistry
  • Procedure steps: 8
  • Total time of stages: 2 h 5 min–2 h 20 min
  • Hydrocarbon range: C₁₀ (n-decane) to C₄₀ (n-tetracontane)
  • Limit of quantification: 0.1 mg/L
  • Working range: 0.1–1 000 mg/L (with dilution)

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.

In the literature the same result is sometimes called TPH (Total Petroleum Hydrocarbons). The standard defines the hydrocarbon oil index through the procedure itself: it is the sum of non-polar compounds extractable with a solvent, not adsorbed on Florisil and eluting on a non-polar GC column between n-decane and n-tetracontane — so the result depends on strict adherence to the procedure, not on the type of oil in the sample.

Cleanup on Florisil is the step that decides the reliability of the result: it is what distinguishes petroleum hydrocarbons from natural organic substances — animal and vegetable fats. Omitting this step inflates the result by biogenic substances, which in wastewater from food-processing plants or car washes can change the assessment of compliance with the permit.

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 range0.1–1 000 mg/L (with dilution)
Boiling temperature of analytes175–525°C
Sample volume1 L (typically)
Precision (CV)5–15 % at concentrations above 1 mg/L
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. Drying of the extract

    Pass the combined extracts through a funnel with anhydrous Na₂SO₄ (about 20 g, calcined). Water remaining in the organic phase spoils the separation on the column and increases detector noise.

    ⏱ Time: 10 min

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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
Ready-made Florisil cartridges (alternative to glass column)Florisil SPE cartridges 6 mL / 1 g15–40 PLN/pc

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 standard—Mineral 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 air—Gases for FID detector. H₂ 5.0, synthetic air (hydrocarbon-free)
Dilute hydrochloric acid (HCl)7647-01-0For acidifying the sample to pH < 2 before extraction
Nitrogen 5.07727-37-9For concentrating the extract in a nitrogen stream, purity 99.999 %

Health and safety (OHS)

Frequently asked questions

Which standard describes this test?

The test is performed according to PN-EN ISO 9377-2:2003 — “Water quality — Determination of hydrocarbon oil index — Part 2: Method using solvent extraction and gas chromatography”.

How does this method work?

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

What is the measuring range and accuracy?

Hydrocarbon range: C₁₀ (n-decane) to C₄₀ (n-tetracontane); Limit of quantification: 0.1 mg/L; Working range: 0.1–1 000 mg/L (with dilution); Boiling temperature of analytes: 175–525°C.

How long does the test take?

The times given for the individual stages add up to approximately 2 h 5 min–2 h 20 min. The procedure comprises 8 steps.

What equipment is required?

Gas chromatograph with FID, Capillary GC column, Autosampler, Extraction system, Florisil column, Evaporator (optional), Ready-made Florisil cartridges (alternative to glass column). Indicative cost of the core instrument (Gas chromatograph with FID): 120 000–300 000 PLN.

Where is this test used?

Monitoring of wastewater from refineries and petrochemical plants; Control of groundwater (fuel contamination from leaking tanks); Study of surface waters (oil spill, ecological disasters); Monitoring of stormwater from fuel stations and parking lots; Control of wastewater from automotive workshops and car washes; Assessment of remediation of sites contaminated with petroleum substances; Assessment of the effectiveness of petroleum substance separators; Study of leachate from waste landfills; Monitoring of wastewater from metalworking plants.

What safety precautions apply?

n-Pentane/n-hexane — extremely flammable! Flash point < -20°C. Work away from ignition sources, fume hood; n-Hexane — neurotoxic with chronic exposure. Work in well-ventilated room; Hydrogen (H₂) — extremely flammable and explosive. Check GC installation tightness; Florisil — irritating dust to respiratory tract. Dust mask when handling; Pentane/hexane waste — flammable organic waste, collect separately; CO₂ or powder extinguisher available near GC station.

Which laboratory can perform this test?

The test is performed by laboratories accredited to ISO/IEC 17025. On LabCoda you can find them by the standard number PN-EN ISO 9377-2.

🔍 Find a laboratory performing this test