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Excess Gibbs Free Energy using Margules Two-Parameter Equation Calculator

Excess Gibbs Free Energy Formula:

\[ G^E = [R] \times T \times x_1 \times x_2 \times (A_{21} \times x_1 + A_{12} \times x_2) \]

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1. What is Excess Gibbs Free Energy?

Definition: Excess Gibbs Free Energy (Gᴱ) is the difference between the actual Gibbs free energy of a solution and what it would have if it were an ideal solution.

Purpose: It quantifies the non-ideality of liquid mixtures and is crucial for understanding phase equilibria in chemical engineering.

2. How Does the Calculator Work?

The calculator uses the Margules two-parameter equation:

\[ G^E = [R] \times T \times x_1 \times x_2 \times (A_{21} \times x_1 + A_{12} \times x_2) \]

Where:

Explanation: The equation accounts for interactions between different molecules in a binary mixture.

3. Importance of Excess Gibbs Free Energy

Details: Gᴱ helps predict vapor-liquid equilibria, activity coefficients, and phase behavior in non-ideal mixtures.

4. Using the Calculator

Tips: Enter temperature in Kelvin, mole fractions (must sum to ≤1), and Margules coefficients. All values must be valid.

5. Frequently Asked Questions (FAQ)

Q1: What are typical values for Margules coefficients?
A: They vary by system but typically range from -1 to 2 for moderately non-ideal mixtures.

Q2: How do I obtain Margules coefficients?
A: They are determined experimentally from vapor-liquid equilibrium data or activity coefficient measurements.

Q3: Can this be used for ternary systems?
A: No, this calculator is specifically for binary systems. Ternary systems require additional parameters.

Q4: What's the relationship between Gᴱ and activity coefficients?
A: The activity coefficients can be derived from the partial derivatives of Gᴱ with respect to composition.

Q5: Why is temperature important in this calculation?
A: Temperature affects molecular interactions and thus the degree of non-ideality in the mixture.

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