Free Vapour Pressure of Water Calculator
Enter temperature, click Calculate
Overview of Water Vapor Pressure and the Calculator
The Water Vapor Pressure Calculator is an online tool designed to compute the saturation vapor pressure of water (or ice) at any specified temperature. It implements five widely used empirical models, including the Antoine equation, Buck formula, Magnus (August–Roche–Magnus) formula, Tetens formula, and a simple exponential correlation. This tool is ideal for researchers, engineers, and students who need a quick and accurate vapor pressure of water at temperature without manual table lookup. It also provides a built‑in water vapor pressure table for instant reference across a range of conditions. Pressures can be displayed in units such as kilopascals (kPa), millimeters of mercury (mmHg), torr, atmospheres (atm), or pascals (Pa).
What Is Vapor Pressure? Definition and Key Factors
Vapor pressure is the equilibrium pressure exerted by a vapor above its condensed phase (liquid or solid) in a closed system at a fixed temperature. At equilibrium, the rate of evaporation from the liquid (or sublimation from the solid) equals the rate of condensation of the vapor — the system is in a dynamic steady state.
Two primary factors influence the vapor pressure of a substance:
- Temperature: As temperature rises, the average kinetic energy of molecules increases, enabling more molecules to overcome intermolecular forces and enter the gas phase. Consequently, vapor pressure increases with temperature. At low temperatures, fewer molecules have sufficient energy, so the vapor pressure is lower.
- Nature of the molecules: Stronger intermolecular forces (e.g., hydrogen bonding, dipole–dipole interactions) make it harder for molecules to escape into the vapor, resulting in a lower vapor pressure. Conversely, substances with weak forces exhibit higher vapor pressures.
Importantly, the surface area of the liquid or solid in contact with the gas does not affect the equilibrium vapor pressure — a wide dish and a narrow tube containing the same liquid at the same temperature will show identical vapor pressure.
Five Empirical Formulas for Water Vapor Pressure
The calculator uses the following equations, each with its own range of applicability and unit conventions:
1. Simple exponential formula (T in Kelvin, P in mmHg):
2. Antoine equation (T in °C, P in mmHg):
3. Magnus (August–Roche–Magnus) formula (T in °C, P in kPa):
4. Tetens formula (T in °C, P in kPa):
5. Buck equation (T in °C, P in kPa):
Accuracy Comparison of the Models
To help users select the most appropriate formula for their application, the table below compares the outputs of each model against the reference data from Lide’s table of water vapor pressures over the temperature range 0 °C to 100 °C (32 °F–212 °F). All pressures are in kPa, and the percentage deviation from the reference is shown in parentheses.
| Temp (°C) | Temp (°F) | Reference (kPa) | Simple (kPa) | Antoine (kPa) | Magnus (kPa) | Tetens (kPa) | Buck (kPa) |
|---|---|---|---|---|---|---|---|
| 0 | 32 | 0.6113 | 0.6593 (+7.85%) | 0.6056 (−0.93%) | 0.6109 (−0.06%) | 0.6108 (−0.09%) | 0.6112 (−0.01%) |
| 20 | 68 | 2.3388 | 2.3755 (+1.57%) | 2.3296 (−0.39%) | 2.3334 (−0.23%) | 2.3382 (+0.05%) | 2.3383 (−0.02%) |
| 35 | 95 | 5.6267 | 5.5696 (−1.01%) | 5.6090 (−0.31%) | 5.6176 (−0.16%) | 5.6225 (+0.04%) | 5.6268 (+0.00%) |
| 50 | 122 | 12.344 | 12.065 (−2.26%) | 12.306 (−0.31%) | 12.361 (+0.13%) | 12.336 (+0.08%) | 12.349 (+0.04%) |
| 75 | 167 | 38.563 | 37.738 (−2.14%) | 38.463 (−0.26%) | 39.000 (+1.13%) | 38.646 (+0.40%) | 38.595 (+0.08%) |
| 100 | 212 | 101.32 | 101.31 (−0.01%) | 101.34 (+0.02%) | 104.08 (+2.72%) | 102.21 (+1.10%) | 101.31 (−0.01%) |
The Lide reference values are taken from standard thermophysical tables.
Key observations:
- The Buck formula consistently produces the smallest absolute error across the entire 0–100 °C window, making it the most reliable single‑choice for general‑purpose calculations.
- The Antoine equation performs well at elevated temperatures but exhibits a noticeable negative bias near 0 °C (−0.93%). Its error, however, remains below ±1% throughout the range, and above 100 °C the Antoine model often becomes the most accurate option.
- The simple exponential yields substantial positive errors at low temperatures (+7.85% at 0 °C) and is therefore recommended only for rough estimations.
- The Magnus and Tetens formulas offer good accuracy in the 0–50 °C interval, but the Magnus error grows rapidly above 75 °C (reaching +2.72% at 100 °C).
The Antoine Equation in Depth
The Antoine equation is derived from the Clausius–Clapeyron relation and is one of the most widely used semi‑empirical correlations for vapor pressure. For water, two sets of Antoine constants are commonly employed:
- Below the normal boiling point (0 °C to 100 °C / 32 °F–212 °F):
(when P is in mmHg and T in °C). - From the boiling point to the critical point (100 °C to 374 °C / 212 °F–705 °F):
A second set of constants is used to maintain accuracy in this higher‑temperature regime. The calculator applies the appropriate constants automatically.
The general form is:
Sometimes the C coefficient is omitted, producing a simpler two‑parameter version, or additional terms are added to increase flexibility.
Quick‑Reference Vapor Pressure Table for Water
For rapid manual lookup, the following table lists saturated water vapor pressures at regular temperature intervals from the freezing point to the boiling point. Values are provided in kPa, torr, and atm.
| Temp (°C) | Temp (°F) | Pressure (kPa) | Pressure (torr) | Pressure (atm) |
|---|---|---|---|---|
| 0 | 32 | 0.6113 | 4.5851 | 0.0060 |
| 5 | 41 | 0.8726 | 6.5450 | 0.0086 |
| 10 | 50 | 1.2281 | 9.2115 | 0.0121 |
| 15 | 59 | 1.7056 | 12.7931 | 0.0168 |
| 20 | 68 | 2.3388 | 17.5424 | 0.0231 |
| 25 | 77 | 3.1690 | 23.7695 | 0.0313 |
| 30 | 86 | 4.2455 | 31.8439 | 0.0419 |
| 35 | 95 | 5.6267 | 42.2037 | 0.0555 |
| 40 | 104 | 7.3814 | 55.3651 | 0.0728 |
| 45 | 113 | 9.5898 | 71.9294 | 0.0946 |
| 50 | 122 | 12.3440 | 92.5876 | 0.1218 |
| 55 | 131 | 15.7520 | 118.1497 | 0.1555 |
| 60 | 140 | 19.9320 | 149.5023 | 0.1967 |
| 65 | 149 | 25.0220 | 187.6804 | 0.2469 |
| 70 | 158 | 31.1760 | 233.8392 | 0.3077 |
| 75 | 167 | 38.5630 | 289.2463 | 0.3806 |
| 80 | 176 | 47.3730 | 355.3267 | 0.4675 |
| 85 | 185 | 57.8150 | 433.6482 | 0.5706 |
| 90 | 194 | 70.1170 | 525.9208 | 0.6920 |
| 95 | 203 | 84.5290 | 634.0196 | 0.8342 |
| 100 | 212 | 101.3200 | 759.9625 | 1.0000 |
These numbers are consistent with the Lide reference and can be used for quick verification of calculations or for educational purposes.
How to Use the Calculator
Operating this tool is extremely simple:
- Enter the temperature in the input field (in °C, °F, or K — the calculator accepts all common units).
- The tool instantly computes the saturation vapor pressure using each of the five formulas.
- The results are displayed side‑by‑side, allowing you to compare the outputs. By default, the Antoine and Buck values are highlighted because they represent the most accurate options for most applications.
- To change the output unit, click on the current unit label and select a different unit from the dropdown (Pa, hPa, kPa, mmHg, torr, atm, etc.).
If a negative temperature (below 0 °C) is entered, the calculator automatically applies the Buck and Tetens models, which are validated for supercooled water and ice. This feature is useful for cold‑region meteorology and frost‑point studies.
Why Water Vapor Pressure Matters
The vapor pressure of water is a critical parameter in many natural and industrial processes. It governs evaporation and condensation rates, influences weather and climate (humidity, cloud formation), and is essential in engineering fields such as air‑conditioning, distillation, and drying. On Earth, the fact that water’s vapor pressure is high enough to permit evaporation but low enough to maintain liquid and solid phases is fundamental to the existence of life as we know it.
By combining multiple empirical models and providing both instant calculation and a reference table, this Water Vapor Pressure Calculator offers a versatile resource for anyone working with water‑vapor‑related data.
FAQ
1. How do I use the Water Vapor Pressure Calculator?
Simply enter the desired temperature in any common unit (°C, °F, or K). The tool instantly displays the saturation vapor pressure computed from all five formulas. You can then change the pressure unit (kPa, mmHg, torr, atm, etc.) from the dropdown menu.
2. Which formula gives the most accurate water vapor pressure?
Across the 0–100 °C range, the Buck equation shows the smallest average deviation from standard reference data. The Antoine equation is also very accurate, especially at higher temperatures, while the simple formula is only suitable for rough estimates.
3. Does the vapor pressure of water depend on the surface area of the container?
No. The equilibrium vapor pressure is a property of the substance and temperature only; it is independent of the liquid’s surface area or the shape of the container.
4. Can I use this calculator to find the vapor pressure of ice?
Yes. When you input a negative temperature (below 0 °C), the calculator automatically applies the Buck and Tetens equations, which are valid for sublimation (ice–vapor equilibrium).
5. Why is water vapor pressure important?
Water vapor pressure determines evaporation and condensation rates, which are vital for the water cycle, weather phenomena, and countless industrial processes. It is also a key factor in humidity control, distillation, and climate science.
How to Use
- Enter the temperature value in the input field.
- Select the temperature unit: Celsius (°C), Fahrenheit (°F), or Kelvin (K).
- Choose the desired pressure unit for the results.
- Click Calculate to see the vapor pressure computed using all five formulas.