💧 Kinematic Viscosity

Petrochemistry PN-EN ISO 3104

Determination of kinematic viscosity of petroleum products using glass capillary viscometer at 40°C and 100°C. Fundamental parameter for oil and fuel classification.

Overview

Kinematic viscosity is a measure of a liquid's resistance to flow under gravity. Expressed in mm²/s (centistokes, cSt), it is one of the most important quality parameters of petroleum products. Classification of lubricating oils SAE, industrial oils ISO VG and fuels is based precisely on kinematic viscosity.

The method involves measuring the time for a defined volume of liquid to flow through a calibrated glass capillary viscometer under gravity at strictly controlled temperature. Kinematic viscosity is calculated as the product of measured flow time and viscometer calibration constant. Measurement is performed standardly at 40°C (for industrial oils) and 100°C (for engine oils, SAE classification).

Excessively high diesel fuel viscosity impedes flow through filters and injectors, reducing engine power. Too low viscosity causes insufficient lubrication of fuel system components. For lubricating oils, viscosity determines oil film thickness, low-temperature pumpability and energy efficiency of machinery. Monitoring oil viscosity in service allows detection of fuel contamination, oxidation or thermal degradation.

The viscosity range covered by the standard is from 0.2 to 300,000 mm²/s at temperatures from -20°C to +150°C. The method includes two procedures: A — with manual glass viscometers, B — with automatic viscometer systems.

Method principle

A calibrated glass capillary viscometer is placed in a thermostatic bath with stability ±0.02°C. After thermal equilibrium is achieved, the sample is aspirated/filled above the upper measurement mark of the viscometer. The time for the liquid meniscus to flow between two measurement marks is measured. Kinematic viscosity is calculated from the formula: ν = C × t, where C is the viscometer calibration constant (mm²/s²) and t is the flow time (s). Flow time should be minimum 200 seconds to ensure accuracy. Minimum two determinations are performed; results should not differ by more than the determinability value stated in the standard.

Applications

Key parameters

ParameterValue
Measurement range0.2–300 000 mm²/s (cSt)
Measurement temperature-20°C to +150°C (typically 40°C and 100°C)
Bath stability±0.02°C
Minimum flow time200 s
Repeatability±0.35% of mean (for Newtonian liquids)
Reproducibility±0.70% of mean

Standard

Standard number
PN-EN ISO 3104:2021
Title (PL)
Przetwory naftowe — Ciecze przezroczyste i nieprzezroczyste — Oznaczanie lepkości kinematycznej i obliczanie lepkości dynamicznej
Title (EN)
Petroleum products — Transparent and opaque liquids — Determination of kinematic viscosity and calculation of dynamic viscosity

Step-by-step procedure

1. Viscometer selection

Select viscometer with range appropriate to expected sample viscosity. Flow time must be min. 200 s. Check viscometer calibration certificate.

⏱ Time: 2 min

2. Bath preparation

Set thermostatic bath to required temperature (40.00°C or 100.00°C). Stability: ±0.02°C. Wait for temperature stabilization.

⏱ Time: 30–60 min • 🌡 Temperature: 40.00°C or 100.00°C

3. Viscometer cleaning

Rinse viscometer sequentially with kerosene, toluene and acetone. Dry by passing clean, dry air. Visually check capillary cleanliness.

⏱ Time: 10 min

4. Viscometer filling

Fill viscometer with sample per manufacturer instructions (approx. 7 mL for Cannon-Fenske). Avoid air bubbles.

⏱ Time: 3 min

5. Thermostating

Place filled viscometer in bath. Wait minimum 30 minutes to achieve thermal equilibrium.

⏱ Time: 30 min • 🌡 Temperature: 40.00 or 100.00°C

6. Flow time measurement

Position liquid meniscus above upper mark. Start timer when meniscus passes upper mark and stop at lower mark.

⏱ Time: >200 s

7. Repeat measurement

Perform second determination on same viscometer (for Ubbelohde type) or on second clean viscometer. Compare results — difference should not exceed determinability.

⏱ Time: >200 s

8. Kinematic viscosity calculation

ν = C × t, where C is viscometer calibration constant, t is average flow time. Report result with appropriate significant figures.

9. Dynamic viscosity calculation (optional)

η = ν × ρ, where ρ is sample density at measurement temperature. Result in mPa·s.

10. Final cleaning

Empty viscometer. Rinse sequentially with kerosene, acetone. Dry and store in vertical position.

⏱ Time: 10 min

Required equipment and apparatus

EquipmentExampleIndicative price
Glass capillary viscometerCannon-Fenske Routine (transparent), Cannon-Fenske Opaque (opaque), Ubbelohde150–600 PLN/pc
Thermostatic viscometer bathTamson TV 4000, Julabo VISCO BATH, Cannon CT-100015 000–45 000 PLN
Calibrated timer/stopwatchDigital timer with ±0.1 s accuracy or automatic optical detector200–500 PLN (manual), 8 000–20 000 PLN (automatic)
Precision thermometerASTM thermometer with 0.01°C resolution or Pt100 sensor500–2 000 PLN
Automatic viscometer systemCannon miniAV, Schott-Geräte AVS 370, Anton Paar SVM 300140 000–120 000 PLN
Suction bulb for filling viscometerRubber bulb with adapter or manual pump50–200 PLN

Reagents, media and consumables

ReagentCASDetails
Viscosity reference oilCertified reference oils (CRM) with known viscosities at 40°C and 100°C, e.g., Cannon S20, S60, S200, N35, N100
Kerosene (cleaning solvent)8008-20-6For initial washing of viscometers after use with oil samples
Acetone67-64-1Purity ≥99.5%, for final rinsing of viscometers
Chromic acid (optional)7738-94-5Chromic mixture for removing stubborn deposits from capillaries (caution: highly corrosive, carcinogenic — limited use)
Toluene108-88-3Purity ≥99.5%, alternative solvent for cleaning viscometers

Health and safety (OHS)

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