Reynolds Number Calculators
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Reynolds Number Formula
Re = ρvD / μ = vD / ν
ρ = fluid density (kg/m³); v = mean flow velocity (m/s); D = characteristic length (m, e.g., pipe diameter); μ = dynamic viscosity (Pa·s = kg/m/s); ν = kinematic viscosity = μ/ρ (m²/s).
For water at 20°C: ρ = 998 kg/m³; μ = 1.002 × 10⁻³ Pa·s; ν = 1.004 × 10⁻⁶ m²/s.
Example: water at 2 m/s in a 5 cm diameter pipe: Re = 2 × 0.05 / 1.004×10⁻⁶ = 99,600 → turbulent.
Flow Regimes
- Laminar: Re < 2,300; smooth parallel flow; no mixing between layers; Hagen-Poiseuille equation applies; pressure drop ∝ velocity
- Transitional: 2,300–4,000; intermittent turbulence
- Turbulent: Re > 4,000; chaotic flow; enhanced mixing; higher pressure loss; friction factor depends on Re and roughness (Moody chart)
Biological Applications
Swimming microorganisms: Re << 1 (Stokes regime) — viscous forces dominate; bacteria swim by rotating helical flagella (screw motion); inertia is irrelevant. Fish: Re ~10⁴–10⁶ — transition from viscous to inertial dominated flow. Blood in aorta: Re ≈ 3,000 (borderline turbulent at peak systole) → heart murmur if turbulence develops. Laminar flow hoods: maintain Re < critical to ensure sterile laminar airflow.
Glossary
Frequently Asked Questions
Re = ρvD/μ. It is the ratio of inertial forces to viscous forces in a fluid flow. Low Re (< 2,300): inertia is negligible relative to viscosity → laminar flow (smooth, layered). High Re (> 4,000): inertia dominates → turbulent flow (chaotic, mixing). Transitional: 2,300–4,000. Practical importance: pipe flow engineering (pump sizing, pressure drop calculations); biological fluid dynamics (blood flow, swimming); chemical mixing (stirred tank reactors); aerodynamics. The same fluid at the same velocity but in a larger pipe (larger D) has a higher Re and is more likely to be turbulent.
Re = ρvD/μ, where v = mean velocity = volumetric flow rate / cross-sectional area = Q/A. Example: water (ν = 1.0 × 10⁻⁶ m²/s) in a 2-cm diameter pipe at 0.5 m/s: Re = vD/ν = 0.5 × 0.02 / 1.0×10⁻⁶ = 10,000 → turbulent. For blood (ν ≈ 3.3 × 10⁻⁶ m²/s) in the aorta (D ≈ 2.5 cm, v ≈ 0.63 m/s at peak systole): Re = 0.63 × 0.025 / 3.3×10⁻⁶ ≈ 4,800 → borderline turbulent. Heart sounds/murmurs can indicate turbulent aortic flow.
Re determines the dominant physics of swimming and fluid transport at different scales: Bacteria (Re ~10⁻⁴): viscosity completely dominates; Stokes flow — if they stop swimming, they stop immediately (no inertial coasting); propulsion must be screw-like (rotating flagella) or oscillatory. Fish (Re ~10⁴–10⁶): inertia increasingly important; body undulation + caudal fin thrust is efficient. Birds/insects in air: Re ~10²–10⁶; wing lift and drag depend on Re. Blood in capillaries (Re ~0.001): laminar; red blood cells line up in single file (Fahraeus-Lindqvist effect). Understanding Re guides design of microfluidic devices, artificial hearts, bioreactors, and drug delivery systems.
For laminar flow (Re < 2,300): pressure drop follows Hagen-Poiseuille law: ΔP = 128 μLQ / (π D⁴); pressure drop is proportional to viscosity and velocity but independent of density and surface roughness. For turbulent flow (Re > 4,000): pressure drop is much higher and depends on: Reynolds number; pipe roughness (relative roughness ε/D); the Darcy-Weisbach equation: ΔP = f × (L/D) × (ρv²/2), where f = Darcy friction factor (from Moody chart). In turbulent flow, doubling flow velocity more than doubles pressure drop (roughly ∝ v²) — much less efficient than laminar flow where ΔP ∝ v. Minimizing Re (laminar flow) reduces pumping energy in pipelines and blood circulation.