Gay-Lussac's Law Calculator

Calculate pressure changes with temperature at constant volume using Gay-Lussac's Law (P₁/T₁ = P₂/T₂) for ideal gas behavior.

Final Pressure (P₂)
220.467 kPa
P₂ = P₁ × T₂ / T₁ (Gay-Lussac's Law)
Pressure Change
20.467 kPa
ΔP = P₂ − P₁
Pressure Ratio
1.1023
P₂ / P₁
Temperature Ratio
1.1023
T₂ / T₁ (in Kelvin)
Percent Pressure Change
10.23%
Percentage change from initial pressure
Initial Temperature (K)
293.15 K
Converted to absolute temperature
Final Temperature (K)
323.15 K
Converted to absolute temperature
Pressure Increase
P₁ = 200.0P₂ = 220.5
Gascp (kJ/kg·K)cv (kJ/kg·K)γR (J/kg·K)
Air1.0050.7181.40287
Nitrogen1.0400.7431.40297
Oxygen0.9180.6581.40260
Helium5.1933.1161.672077
CO₂0.8440.6551.29189
Argon0.5200.3121.67208
Planning notes, formulas, and examples

About the Gay-Lussac's Law Calculator

Gay-Lussac's Law (also called Amontons' Law) states that the pressure of an ideal gas is directly proportional to its absolute temperature when the volume is held constant: P₁/T₁ = P₂/T₂. Heat a sealed container and the pressure rises; cool it and the pressure drops.

This fundamental gas law explains everyday phenomena — why tire pressure increases on a hot day, why aerosol cans warn against heating, and why pressure cookers reach higher temperatures. It is one of the three classical gas laws (along with Boyle's and Charles') that combine into the ideal gas law PV = nRT.

This Gay-Lussac's Law Calculator lets you find the final pressure after a temperature change, the required temperature for a desired pressure, or verify the initial conditions. It supports multiple pressure units (kPa, atm, psi, bar) and temperature scales (°C, K, °F). Preset buttons cover tire inflation, pressure cooker operation, engine combustion, and cryogenic scenarios. A reference table lists thermodynamic properties for common gases.

When This Page Helps

Use this calculator when you need to estimate how pressure changes in a sealed gas system as temperature rises or falls at constant volume. It is particularly useful for quick safety and operating checks on tires, tanks, cans, and other closed gas volumes. It also helps explain why a moderate temperature change can matter in a confined gas system.

How to Use the Inputs

  1. Enter the initial gas pressure in your chosen unit.
  2. Select the pressure unit (kPa, atm, psi, or bar).
  3. Enter the initial temperature in °C, K, or °F.
  4. Enter the final temperature.
  5. Select what to solve for: final pressure, final temperature, or initial pressure.
  6. Review the calculated values, ratios, and percentage change.
  7. Use presets for common scenarios like tire inflation or pressure cookers.
Formula used
Gay-Lussac's Law: P₁ / T₁ = P₂ / T₂ (constant volume) P₂ = P₁ × (T₂ / T₁) T₂ = T₁ × (P₂ / P₁) All temperatures must be in Kelvin (absolute).

Example Calculation

Result: P₂ = 220.45 kPa

Heating a sealed container from 20°C to 50°C raises the pressure from 200 kPa to 220.45 kPa — a 10.2% increase.

Tips & Best Practices

  • Always convert temperatures to Kelvin before applying the proportional form of the law.
  • Small temperature increases can create meaningful pressure changes in sealed systems such as tires, tanks, and aerosol containers.
  • If the vessel can expand noticeably, the constant-volume assumption becomes weaker and the simple relation loses accuracy.
  • This law is most reliable when the gas remains well away from condensation and extreme non-ideal conditions.

What Stays Constant

Gay-Lussac's law only applies cleanly when the amount of gas and the container volume stay constant. If gas escapes, the vessel flexes, or the gas undergoes phase change, the simple proportionality between pressure and temperature no longer tells the full story.

Everyday Interpretation

This is why tire pressures climb after driving, why sealed cans can rupture when overheated, and why pressure vessels are rated with thermal conditions in mind. The law is simple, but it has very practical safety implications whenever a gas is trapped in a fixed volume.

Common Mistakes

The biggest error is using Celsius or Fahrenheit directly in the ratio instead of absolute temperature. The second is forgetting that gauge pressure and absolute pressure are not the same quantity in thermodynamic calculations.

Sources & Methodology

Last updated:

Frequently Asked Questions

  • It assumes an ideal gas at constant volume. Real gases deviate at very high pressures or low temperatures.