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Chemical Engineering Thermodynamics CME 311

Reactions Equilibria

Chapter 13

1

Reaction Equilibria in an Ideal Gas

Let’s define a new term: Standard Gibbs Energy Change of Reaction = ΔGᵒ(T)

This can be rearranged to the following…

Remember when we did standard heat of reactions in Chpt 4? This is a similar concept but for G

Standard Reference State

Standard state = Species in their natural form at 298 K and 1 atm

ΔGᵒf,298,i = standard G of formation of species i at 298 K

Analogous to ΔH from previous section

Data given in Table C.4

Standard Gibbs Example

Example: What is the standard G of formation for the following reaction?

Reaction Equilibria in an Ideal Gas

π is the product of species

Keq (T) = Dimensionless equilibrium constant of the reaction, as a function of T

Standard Gibbs/keq Example

Example: What is the keq for the following reaction at 298K?

Ideal Gas Reaction example:

The following ideal gas reaction occurs at 2 atm and 300 K.

If you initially have 100 mol A and 50 mol B with a keq of 0.05, what is the extent of reaction and conversion of A and B?

Ideal Gas Reaction Example

Example #2

For the following reaction, occurring at standard state, determine the keq

Reaction Efficiency

What can you do to increase the conversion of reactions and improve reaction efficiency?

Decrease the pressure

Remove the products as they are formed

System will continue to react in order to achieve equilibrium

Change your reaction temperature

Increase T if endothermic rxn (ΔHᵒ > 0)

Decrease T if exothermic rxn (ΔHᵒ < 0)

**This is the most common industrial answer

Modifying reaction temperature

How does temperature impact keq?

Why? Because ΔG298 can only be applied for systems at 298 K and ΔG varies with temperature

If you are curious, your book goes through this derivation in detail…

Procedure:

Find keq at 298 K = k1

Use above equation to solve for k2 … keq at modified temperature

Modified Rxn Temp: Example

Again, let’s consider the following reaction.

We previously determined that at 298 K and 1 atm the keq was 3.86 x 10-8

A) What would the new keq be if we raised the reaction temperature to 625 K?

B) If we started with 1 mole of C3H8, what would be the conversion?

Modified Rxn Temp: Example

Influence of Cp as a function of T

In this example, we assumed that Cp (ΔH) was independent of temperature

We previously discussed how both do vary with T (Chpt. 4)

What would happen if we repeat this example but take the temperature dependence into account?

We will not be doing this due to the complexity and length of this analysis

We would find:

ξ = 0.78 and X = 78%

Not much difference!

How do we know if we can neglect heat effects?

Determine Cp at both inlet and outlet conditions and see if there is much change

Reactions in Ideal liquid phase

A liquid phase is ideal when:

All the molecules are similar

All the molecules behave similarly

There are no unusual inter-molecule interactions

Examples of ideal liquids:

Hexane (C6H12) and Pentane (C5H10)

Methanol (CH4O) and Ethanol (C2H6O)

Reactions in ideal liquid phase

Superscript “id” = ideal solution

Where xi is the liquid mole fraction of i and HiL is the H of pure I in the liquid phase at T and P of the system

Similarly, it can be shown:

Chemical potential in i.d. liquid reactions

Recall:

Through application of the incompressible assumption and derivation we arrive at the following equation:

Reaction equilibria in ideal liquids

We showed earlier that:

Therefore, for an ideal solution:

After going through the same derivation as for an ideal gas:

Ideal Liquid Rxn Example:

The following reaction takes place at 350 K with a keq of 1.89.

If the reaction starts with 100 mol AA and 100 mol M, what is the extent of reaction? You may assume the liquid phase is ideal.

Ideal Liquid Rxn Example:

Non-Ideal Liquids

Introduce the term GE = Excess Gibbs energy

Excess

G

“Real”

G

Ideal

G

Activity Coefficient

Let’s define:

γ = Activity coefficient

Represents a measure of non-ideality for solutions

Due to the intermolecular interactions

If we have an ideal solution γ = 1

μ can be expressed as:

Leads to

Rxn. Equilibria for non-ideal solutions

We showed earlier that:

Going through rearrangement:

Reaction Equilibrium expression for Non-ideal solutions

How do we find γ?

For an ideal liquid, γ = 1

For a non-ideal liquid:

Several models for finding GE exist

You book goes through several techniques, starting on page 446

We are going to discuss one in particular – Margueles Equation

Margueles Equation

For a binary mixture:

Recall, γ can be expressed as….

Simultaneous solving of these 2 equations leads to:

Where A is a measure of interaction between the particles

While this is relatively straight-forward for a binary system, this rapidly gets complex for a multi-component system (n > 2).

Margueles Derivation

Let’s return to our previous example:

The following reaction takes place at 350 K with a keq of 1.89.

If the reaction starts with 100 mol AA and 100 mol M, what is the extent of reaction?

Now, assume that that is a non-ideal solution!

Included is the following table

AA M MA W
ln γ 7.8 3.3 9.8 2.1

Non-ideal liquid example

Non-Ideal Liquid Example

Given the following Rxn and expressions for the activity coefficients, T = 50 deg C, and an extent of reaction of 0.73, find keq. You start with 1 mole of A

Non-Ideal Liquid Example

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