Calculation of Water Vapor Pressure

Understanding the Calculation of Water Vapor Pressure: Fundamentals and Applications

Water vapor pressure quantifies the pressure exerted by water molecules in the gas phase. Calculating it accurately is essential in many scientific and engineering fields.

This article explores the core formulas, variable definitions, extensive data tables, and real-world applications of water vapor pressure calculation.

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  • Calculate water vapor pressure at 25°C using Antoine equation.
  • Determine saturation vapor pressure at 100°C for steam generation.
  • Find partial vapor pressure in humid air at 30°C and 60% relative humidity.
  • Compute dew point temperature from given vapor pressure data.

Comprehensive Tables of Water Vapor Pressure Values

Water vapor pressure varies significantly with temperature. The following tables provide saturation vapor pressure values over liquid water and ice at common temperatures, essential for engineers and scientists.

Temperature (°C)Saturation Vapor Pressure (kPa)Saturation Vapor Pressure (mmHg)Saturation Vapor Pressure (Pa)
00.6114.58611
50.8726.54872
101.2289.211228
151.70512.791705
202.33817.532338
253.16923.763169
304.24631.854246
355.62842.215628
407.38455.387384
5012.3592.6312350
6019.94149.5519940
7031.15233.6331150
8047.37355.2847370
9070.12525.9070120
100101.42760.00101420

These values are critical for processes such as HVAC design, meteorology, and chemical engineering where vapor-liquid equilibrium is involved.

Fundamental Formulas for Calculating Water Vapor Pressure

Several empirical and semi-empirical formulas exist to calculate water vapor pressure, each with specific ranges of validity and accuracy. Below are the most widely used equations along with detailed explanations of their variables.

Antoine Equation

The Antoine equation is a popular empirical relation to estimate saturation vapor pressure over liquid water:

psat = 10A – (B / (C + T))
  • psat: Saturation vapor pressure (usually in mmHg)
  • T: Temperature in °C
  • A, B, C: Empirical constants specific to the substance and temperature range

For water, typical constants valid between 1°C and 100°C are:

  • A = 8.07131
  • B = 1730.63
  • C = 233.426

This formula provides good accuracy for vapor pressure calculations in the liquid phase.

Magnus-Tetens Approximation

Widely used in meteorology, the Magnus-Tetens formula estimates saturation vapor pressure over water:

psat = 0.61094 Ɨ exp((17.625 Ɨ T) / (T + 243.04))
  • psat: Saturation vapor pressure in kPa
  • T: Temperature in °C

This formula is valid approximately between -45°C and 60°C and is favored for its simplicity and reasonable accuracy.

Goff-Gratch Equation

The Goff-Gratch equation is a more complex, highly accurate formula used for saturation vapor pressure over water and ice, especially in atmospheric sciences:

log10(psat) = -7.90298 Ɨ (373.16 / TK – 1) + 5.02808 Ɨ log10(373.16 / TK) – 1.3816 Ɨ 10-7 Ɨ (1011.344 Ɨ (1 – TK / 373.16)) + 8.1328 Ɨ 10-3 Ɨ (10-3.49149 Ɨ (373.16 / TK – 1)) + log10(1013.246)
  • psat: Saturation vapor pressure in hPa
  • TK: Temperature in Kelvin (K = °C + 273.15)

This equation is often used in climate modeling and atmospheric research due to its precision.

Clausius-Clapeyron Equation

The Clausius-Clapeyron relation describes the phase equilibrium between liquid and vapor phases, providing a theoretical basis for vapor pressure dependence on temperature:

ln(psat) = – (Ī”Hvap / R) Ɨ (1 / T) + C
  • psat: Saturation vapor pressure (Pa)
  • Ī”Hvap: Enthalpy of vaporization (J/mol)
  • R: Universal gas constant (8.314 J/molĀ·K)
  • T: Absolute temperature in Kelvin
  • C: Integration constant determined experimentally

This equation is fundamental in thermodynamics and is used to derive other empirical formulas.

Detailed Explanation of Variables and Typical Values

  • Temperature (T): The independent variable, usually in °C or K. Accurate temperature measurement is critical as vapor pressure is highly temperature-dependent.
  • Saturation Vapor Pressure (psat): The pressure exerted by vapor in equilibrium with its liquid or solid phase at a given temperature.
  • Empirical Constants (A, B, C): Determined by fitting experimental data; vary depending on temperature range and phase (liquid or ice).
  • Enthalpy of Vaporization (Ī”Hvap): For water, approximately 40.65 kJ/mol at 100°C, decreases slightly with temperature.
  • Universal Gas Constant (R): 8.314 J/molĀ·K, a fundamental constant in thermodynamics.

Real-World Applications and Case Studies

Case 1: HVAC System Design – Calculating Humidity Control Parameters

In heating, ventilation, and air conditioning (HVAC) systems, controlling indoor humidity is vital for comfort and health. Engineers must calculate the partial pressure of water vapor in air to design dehumidification or humidification processes.

Suppose an HVAC engineer needs to determine the saturation vapor pressure at 25°C to assess the maximum moisture content air can hold. Using the Antoine equation:

psat = 108.07131 – (1730.63 / (233.426 + 25))

Calculating the denominator:

233.426 + 25 = 258.426

Then:

1730.63 / 258.426 ā‰ˆ 6.693

So the exponent is:

8.07131 – 6.693 = 1.37831

Therefore:

psat = 101.37831 ā‰ˆ 23.9 mmHg

Converting to kPa (1 mmHg = 0.133322 kPa):

23.9 Ɨ 0.133322 ā‰ˆ 3.19 kPa

This value matches the tabulated data and informs the maximum moisture content for air at 25°C, critical for sizing humidifiers or dehumidifiers.

Case 2: Meteorological Analysis – Determining Dew Point Temperature

In meteorology, dew point temperature is the temperature at which air becomes saturated with moisture, causing condensation. Given ambient temperature and relative humidity, the vapor pressure can be calculated, then the dew point derived.

Assume air temperature T = 30°C and relative humidity RH = 60%. First, calculate saturation vapor pressure at 30°C using Magnus-Tetens:

psat = 0.61094 Ɨ exp((17.625 Ɨ 30) / (30 + 243.04)) = ?

Calculate the exponent:

(17.625 Ɨ 30) / (273.04) ā‰ˆ 1.935

Exponentiating:

exp(1.935) ā‰ˆ 6.92

Therefore:

psat = 0.61094 Ɨ 6.92 ā‰ˆ 4.23 kPa

Calculate actual vapor pressure (pv):

pv = RH Ɨ psat = 0.60 Ɨ 4.23 = 2.54 kPa

To find dew point temperature (Td), invert Magnus-Tetens:

Td = (243.04 Ɨ ln(pv / 0.61094)) / (17.625 – ln(pv / 0.61094))

Calculate ln(pv / 0.61094):

ln(2.54 / 0.61094) = ln(4.16) ā‰ˆ 1.426

Calculate numerator and denominator:

Numerator = 243.04 Ɨ 1.426 = 346.7
Denominator = 17.625 – 1.426 = 16.199

Finally:

Td = 346.7 / 16.199 ā‰ˆ 21.4°C

The dew point is approximately 21.4°C, indicating the temperature at which condensation begins under these conditions.

Additional Considerations and Advanced Topics

Water vapor pressure calculations are influenced by factors such as atmospheric pressure, presence of solutes, and phase changes. For example, vapor pressure lowering occurs in solutions (Raoult’s Law), and non-ideal gas behavior can affect accuracy at high pressures.

Advanced models incorporate these effects, such as the Antoine equation modifications for pressure dependence or the use of thermodynamic databases like NIST REFPROP for precise calculations.

  • Raoult’s Law: pv = xsolvent Ɨ psat, where xsolvent is mole fraction of solvent.
  • Non-ideal Gas Corrections: Fugacity coefficients adjust vapor pressure for real gas behavior.
  • Phase Equilibria: Vapor pressure over ice differs from liquid water, important in cold climate studies.

Authoritative Resources for Further Study

Mastering the calculation of water vapor pressure enables precise control and prediction in diverse fields, from climate science to industrial process engineering.