Q. how to calculate partial pressure

Answer

Dalton’s law gives the partial pressure of component i as
\[
p_i = x_i P_{\text{tot}} = \frac{n_i}{n_{\text{tot}}} P_{\text{tot}}.
\]
Using the ideal gas law for the component you may also write
\[
p_i = \frac{n_i R T}{V}.
\]
Compute \(x_i=\frac{n_i}{n_{\text{tot}}}\) and multiply by \(P_{\text{tot}}\) or use \(p_i=\frac{n_i R T}{V}\) when \(n_i,R,T,V\) are known.

Detailed Explanation

Definition and fundamental law. Dalton’s law states that the total pressure of a mixture of ideal gases equals the sum of the partial pressures of each gas. A compact form is

\[ P_{\text{total}} \;=\; \sum_{i} P_{i} \]

Meaning of partial pressure. The partial pressure of a gas in a mixture is the pressure that gas would exert if it alone occupied the whole volume at the same temperature. Two common ways to calculate a partial pressure are by using mole fraction or by using the ideal gas law for that component.

Mole fraction method. First compute the mole fraction of species i using

\[ x_{i} \;=\; \frac{n_{i}}{n_{\text{total}}} \]

Then obtain the partial pressure from the total pressure by

\[ P_{i} \;=\; x_{i}\,P_{\text{total}} \]

Ideal gas method for a component. If you know the number of moles of species i, the temperature and the common volume, you can use the ideal gas law for that component directly:

\[ P_{i} \;=\; \frac{n_{i} R T}{V} \]

Because the same \( R \), \( T \), and \( V \) apply to every component, summing the component pressures reproduces the total pressure. That is,

\[ P_{\text{total}} \;=\; \frac{n_{\text{total}} R T}{V} \;=\; \sum_{i} \frac{n_{i} R T}{V} \;=\; \sum_{i} P_{i} \]

Step by step procedure summary. Step 1. Determine the number of moles \( n_{i} \) of each gas present. Step 2. Compute total moles \( n_{\text{total}}=\sum_{i} n_{i} \). Step 3. If total pressure is known, compute mole fractions \( x_{i}=n_{i}/n_{\text{total}} \) and then \( P_{i}=x_{i}P_{\text{total}} \). Step 4. If total pressure is not given but temperature and volume are given, compute total pressure using \( P_{\text{total}}=n_{\text{total}}RT/V \) and then use step 3, or compute each \( P_{i}=n_{i}RT/V \) directly. Step 5. Check that the sum of calculated partial pressures equals the total pressure within rounding error.

Worked example A known total pressure. Suppose a mixture contains 1.00 mol of gas A and 3.00 mol of gas B and the measured total pressure is 4.00 atm. Step A1 compute total moles

\[ n_{\text{total}}=1.00+3.00=4.00\ \text{mol} \]

Step A2 compute mole fractions

\[ x_{A}=\frac{1.00}{4.00}=0.250 \qquad x_{B}=\frac{3.00}{4.00}=0.750 \]

Step A3 compute partial pressures

\[ P_{A}=x_{A}P_{\text{total}}=0.250\times 4.00\ \text{atm}=1.00\ \text{atm} \]

\[ P_{B}=x_{B}P_{\text{total}}=0.750\times 4.00\ \text{atm}=3.00\ \text{atm} \]

Worked example B using ideal gas law. Suppose a 10.0 L container at 298 K contains 2.00 mol O2 and 3.00 mol N2. Use \( R=0.082057\ \text{L atm mol}^{-1}\text{K}^{-1} \). Step B1 total moles

\[ n_{\text{total}}=2.00+3.00=5.00\ \text{mol} \]

Step B2 compute total pressure

\[ P_{\text{total}}=\frac{n_{\text{total}} R T}{V}=\frac{5.00\times 0.082057\times 298}{10.0}=12.2265\ \text{atm (approximately)} \]

Step B3 compute partial pressures directly or via mole fraction. Mole fraction of O2 is \( x_{\text{O}_{2}}=2.00/5.00=0.400 \). Then

\[ P_{\text{O}_{2}}=x_{\text{O}_{2}}P_{\text{total}}=0.400\times 12.2265=4.8906\ \text{atm (approximately)} \]

Alternatively direct ideal gas calculation for O2 gives the same result

\[ P_{\text{O}_{2}}=\frac{n_{\text{O}_{2}} R T}{V}=\frac{2.00\times 0.082057\times 298}{10.0}=4.8906\ \text{atm} \]

Step B4 for N2

\[ P_{\text{N}_{2}}=\frac{3.00\times 0.082057\times 298}{10.0}=7.3359\ \text{atm} \]

Consistency check

\[ P_{\text{O}_{2}}+P_{\text{N}_{2}}=4.8906+7.3359=12.2265\ \text{atm}=P_{\text{total}}\ ]

Units and common pitfalls. Ensure consistent units for R, volume, pressure, and temperature. Use R appropriate to the pressure units desired. When gases are not ideal at high pressures or low temperatures, corrections are needed but Dalton’s law for partial pressures still applies to partial pressures of each species in the real mixture if measured experimentally.

Quick checklist for solving a partial pressure problem. 1 Identify known quantities. 2 Choose mole fraction method if total pressure known. 3 Choose ideal gas method if n, T, V known. 4 Compute partial pressures. 5 Verify sum equals total pressure.

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Chemistry FAQs

What is partial pressure

Partial pressure is the pressure single gas would exert alone in the same volume and temperature. By Dalton s law \(P_{i}=x_{i}P_{\text{tot}}\) where \(x_{i}=\frac{n_{i}}{\sum_{j}n_{j}}\) is the mole fraction and \(P_{\text{tot}}\) is the total pressure.

How do you calculate partial pressure from moles

Compute the mole fraction \(x_{i}=\frac{n_{i}}{\sum_{j}n_{j}}\) then \(P_{i}=x_{i}P_{\text{tot}}\). Alternatively in fixed volume use the ideal gas law per component \(P_{i}=\frac{n_{i}RT}{V}\) with consistent units for \(R,T,V\).

How to get partial pressure from percent composition by volume or mole

If percent is by mole or volume, convert to fraction \(f=\%\!/100\). Then \(P_{i}=fP_{\text{tot}}\). Percent by mass requires conversion to moles first, using molar masses, then use mole fraction.

How to correct for water vapor when measuring gas pressure

Subtract water vapor pressure: \(P_{\text{dry gas}}=P_{\text{atm}}-P_{\text{H}_{2}\text{O}}\), where \(P_{\text{H}_{2}\text{O}}\) is the vapor pressure at the temperature. Then use mole fractions if needed to find each component s partial pressure.

How to calculate partial pressures in reaction at equilibrium using Kp

Use \(K_{p}=\prod_{i}P_{i}^{\nu_{i}}\) with stoichiometric exponents. Express each \(P_{i}\) in terms of an unknown (for example change variable \(x\) and total pressure) and solve for \(x\). Then compute each \(P_{i}\) from stoichiometry.

What units should I use and how to convert

Use consistent units for \(R\), \(T\) and \(V\). Commonly \(R=0.08206\) L atm mol^{-1} K^{-1}, so use atm, L, mol, K. To convert Pto atm use \(1\ \text{atm}=101325\ \text{Pa}\).

How to find partial pressure if gases are non ideal

Replace pressures with fugacities: \(f_{i}=\phi_{i}P_{i}\). Solve using fugacity coefficients \(\phi_{i}\) from an equation of state or experimental data. For small deviations use virial or van der Waals corrections.

How to compute partial pressure when volumes change or gases are collected over water

If volume changes, recompute \(P_{i}\) with \(P_{i}=\frac{n_{i}RT}{V_{\text{new}}}\). When collecting gas over water, subtract water vapor pressure from the total to get the gas mixture pressure, then apply mole fractions if mixture contains multiple gases.
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