Mass transfer · Calculator

Schmidt number calculator (Sc)

Calculate the Schmidt number from viscosity, density and molecular diffusivity. Use it for the spreading of a particular species, not of heat.

Enter values and calculate

Sc = μ / (ρD)

Result

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How Sc differs from Pr

Sc = μ/(ρD) = ν/D compares how fast momentum spreads with how fast the concentration of a species spreads. It is the Prandtl number with mass diffusivity D in place of thermal diffusivity α, which is why it is sometimes called the mass-transfer Prandtl number. Sc above 1 means the concentration boundary layer tends to be thinner than the velocity boundary layer.

Variables and SI units

Inputs of the Schmidt number calculator
SymbolMeaningSI unitExample
μDynamic viscosity of the carrier fluidPa·s0.001
ρDensity of the carrier fluidkg/m³1000
DMolecular diffusivity of the species in that fluidm²/s1e-9

Choosing a value of D

Reading the result

The example assumes a solute in water: μ = 0.001 Pa·s, ρ = 1000 kg/m³ and D = 1×10⁻⁹ m²/s, so Sc = 1000. Gas mixtures often have Sc around 1, while solutes in liquids commonly reach hundreds or more. In the same flow, heat can spread widely while a solute stays in a thin layer.

If the result lands far outside these ranges, at 0.01 or 10⁶ for example, suspect the units of D first. Entering a cm²/s value without converting makes Sc exactly 10⁴ times too small.

Oceanographers use temperature-dependent Schmidt numbers to estimate how fast gases cross the sea surface; the reference manual of the R package marelac describes this use.

Link to the Péclet number

With the same length and speed, the mass Péclet number is Re × Sc. The thermal and mass diffusion note uses v = 0.2 m/s and L = 0.05 m to get Re = 10000 and Sc = 1000, so the mass Péclet number is 10⁷. The same note shows that over 0.25 s the diffusion length √(Dt) is about 0.01581 mm, far shorter than the thermal length of 0.2236 mm. Entering D in the α field of the Péclet calculator gives the mass Péclet number directly.

Moving table data into the calculator

Example 1. Oxygen in 40 °C water, and the cm²/s slip

Given: Water at 40 °C has ρ = 992.2 kg/m³, μ = 6.529×10⁻⁴ Pa·s, ν = 0.6581×10⁻⁶ m²/s and Pr = 4.341 (IAEA Table 3.3, saturated liquid used as a low-pressure approximation). Cornell lists the oxygen diffusivity at 40 °C as 0.0000324 cm²/s (a Wilke–Chang estimate).

Unit conversion: 0.0000324 cm²/s × 10⁻⁴ = 3.24×10⁻⁹ m²/s.

Calculator input: μ = 6.529e-4, ρ = 992.2 and D = 3.24e-9 give Sc = 203.1. Checking with ν/D = 0.6581×10⁻⁶ ÷ 3.24×10⁻⁹ also gives 203.1. Sc/Pr = 46.79, so at this temperature oxygen still spreads about 47 times more slowly than heat.

Common slip: Skipping the conversion and entering D = 3.24e-5 gives Sc = 0.0203, smaller than for a gas. A liquid-phase solute with Sc below 1 is a reason to recheck units.

Example 2. Oxygen in 60 °C air: matching the pressure

Given: IAEA Table 3.1 gives dry air at 98.1 kPa and 60 °C as ρ = 1.026 kg/m³ and μ = 20.10×10⁻⁶ Pa·s. Cornell's gas-diffusion page lists D = 0.274 cm²/s for the oxygen-nitrogen pair at atmospheric pressure (1 atm) and 60 °C. Air is approximated as nitrogen.

Pressure correction: Treating gas diffusivity as inversely proportional to pressure at fixed temperature, move D to 98.1 kPa: 2.74×10⁻⁵ × 101.325 / 98.1 = 2.830×10⁻⁵ m²/s.

Calculator input: μ = 20.10e-6, ρ = 1.026 and D = 2.830e-5 give Sc = 0.692. Mixing the uncorrected 1 atm D with the 98.1 kPa density gives 0.715, about 3.3% high.

Judgment: In a gas both ν and D scale inversely with pressure, so Sc itself barely depends on pressure; the error comes from mixing data at different pressures. The guide's example gives Sc = 0.690 for oxygen in 20 °C air, so a 40 K rise hardly changes Sc in the gas, whereas the same rise cuts Sc for oxygen in water by more than a factor of five.

Schmidt calculator input questions

I only know ν. How do I fill the μ and ρ fields?

Since Sc = μ/(ρD) = ν/D, entering ν in the μ field and 1 in the ρ field gives the same result. With ν = 0.6581×10⁻⁶ m²/s from Example 1 and ρ = 1, Sc = 203.1. If you will reuse μ and ρ in other calculations, entering the real values avoids confusion.

Which D do I use for a solution with several species?

Compute Sc separately for each species of interest. Each species has its own D in the same solvent, and therefore its own Sc. For dilute solutions the solvent properties μ and ρ can be approximated by those of the pure solvent.

What if I need a value between the temperatures in the Cornell table?

Linear interpolation gives a rough value, but liquid-phase D is temperature-sensitive enough to more than double between 20 °C and 60 °C. Pair the interpolated D with μ and ρ at the same temperature, and expect the ±10% uncertainty of the underlying estimate on top.

Related guides and calculators

Guide

Calculation notes

Related calculators

References