Gibbs Energy Change and Equilibrium

Energy can take many forms, including kinetic energy produced by an object’s movement, potential energy produced by an object’s position, heat energy transferred from one object to another due to a temperature difference, radiant energy associated with sunlight, the electrical energy produced in galvanic cells, the chemical energy stored in chemical substances, and so on. All of these different types of energy may be transformed from one form to the other.

For example, as water in a dam reservoir falls, its potential energy is turned into kinetic energy, and if the falling water is utilized to power turbines, the kinetic energy of the water is converted into electrical energy. However, if the water collides with rocks near the dam’s base. The kinetic energy of the object is transformed into thermal energy. 

As a result, the various kinds of energy are quantitatively tied to one another. Thermodynamics is the study of such quantitative relationships between various kinds of energy. Energy shifts occur as a result of physical and chemical processes. The study of energy transitions in these processes is the main focus of thermodynamics.

Thermodynamics is the branch of science that studies the many kinds of energy, their quantitative connections, and the energy changes that occur in physical and chemical processes. 

Gibbs Energy

J.W. Gibbs was an American theoretician. He introduced a new thermodynamic function called Gibbs energy denoted as G. The second law of thermodynamics states that ΔS_total = (ΔS_system + ΔS_Surrounding) must be positive for all spontaneous processes. To assess the spontaneity of a process, two entropy changes, ΔS_System and ΔS_Surrounding must be determined. As a result, it is more straightforward to describe the criteria of spontaneity in terms of the system’s thermodynamic features alone, without respect for the surroundings and this problem was solved by Gibbs.

Gibbs energy (G) is defined as,

G = H – TS

where:

• S is the entropy of the system,
• H is Enthalpy, and
• T is the Temperature.

G is also a state function because, H, T, and S are state functions. 

The change in Gibbs Energy (ΔG) on the initial and final state of the system and not on the path connecting the two states. The change in Gibbs energy at constant temperature and pressure is defined as:

ΔG = ΔH – T ΔS

where:

• ΔS is the change in entropy of the system and
• ΔH is the change in Enthalpy.

Gibbs Energy and Spontaneity

The total entropy change can be written as,

ΔS_total = ΔS_system + ΔS_surrounding = ΔS + ΔS_surr

According to the second law of thermodynamics, ΔS_total > 0 at constant temperature and pressure for the process to be spontaneous. If ΔH is the enthalpy change accompanying the reaction, that is the enthalpy change of the system then the change in enthalpy of the surroundings is (-ΔH)

Therefore,

ΔS_surr = -ΔH / T

Hence the total entropy is given by,

ΔS_total = ΔS – ΔH / T   

This equation shows that ΔS_total is expressed in terms of the properties of the system only.

Rearranging the equation we get,

-T ΔS_total = -T ΔS + ΔH

or

-T ΔStotal = ΔH -T ΔS 

Combining the above two equations, we get,

ΔG = -T ΔS_total    

This equation indicates that ΔG and ΔS_total have opposite signs because T is always positive. Thus, for a spontaneous process carried out at a constant temperature and pressure ΔS_total  > 0 and hence ΔG < 0.

Gibbs energy of a system decreases in a spontaneous change that takes place at constant temperature and pressure. On contrary, for a non-spontaneous reaction ΔS_total and hence ΔG > 0.

Gibbs energy of a system increases in a non-spontaneous change that takes place at constant temperature and pressure. The end of the spontaneous process is an equilibrium that corresponds to a minimum in G. Hence the change in Gibbs energy is:

• ΔG < 0, the process is spontaneous.
• ΔG > 0, the process is non-spontaneous.
• ΔG = 0, the process is at equilibrium.

Factor affecting the Spontaneity

Consider the equation,

ΔG = ΔH – T ΔS

The value ΔG determines whether a physical or chemical change will occur spontaneously. The equations ΔH and ΔS correspond to the values of the system alone. The equation states that two elements influence the spontaneity of reactions

• ΔH is the amount of heat transmitted at constant pressure and temperature, and
• ΔS is the rise or reduction in molecular disorder.

The spontaneous process is favoured by a decrease in enthalpy (-ΔH) and increase in entropy (ΔS) On the other hand non-spontaneous reaction is favoured by an increase in enthalpy (+ΔH) and decrease in entropy (-ΔS). The term temperature in the equation is an important component in determining the relative relevance of the enthalpy and entropy contributions to ΔG. If ΔH and ΔS in the equation are both positive or both negative, the sign of ΔG and hence the spontaneity of the reaction, depends on temperature. 

Temperature of Equilibrium

At equilibrium, i.e., ΔG = 0, the process is neither spontaneous nor non-spontaneous because it is balanced between spontaneous and non-spontaneous behavior. (+ΔH)

So, 

ΔG = ΔH – T ΔS = 0

Hence,

ΔH = TΔS or T = ΔH / ΔS

T is the temperature at which the transition from spontaneous to non-spontaneous behavior happens. T is calculated on the assumption that ΔH and ΔS are temperature independent. In reality, ΔH and ΔS change with temperature. However, for modest temperature changes, the variance in them will not add considerable mistakes. 

ΔG and Equilibrium constant

All of the substances (reactants and products) in a chemical reaction may not be in their normal forms. As a result of the connection, the change in Gibbs energy of a reaction is related to the change in standard Gibbs energy. 

ΔG = ΔG° + RT ln Q

where:

• ΔG° is the standard Gibbs energy change (change in Gibbs energy when all the substances are in their standard state).
• Q is the reaction quotient.

The expression of the reaction quotient is similar to that of the equilibrium constant, but there is one single difference between them, i.e., Equilibrium concentrations or partial pressures of products and reactants are included in the equilibrium constant. Whereas Q is expressed in terms of reactant beginning concentration partial pressures and product final concentrations or pressures. 

For Example, consider the below example:

aA +bB ⇢ cC + dD

For the above reaction, the reaction Quotient is given by 

or

When the values of concentration or partial pressure are other than equilibrium values. When the reaction reaches equilibrium, the concentrations and partial pressure reach their equilibrium values and at this stage, Q = K. At equilibrium, ΔG = 0 and Q = K, then the standard Gibbs energy equation becomes,

0 = ΔG° + RT ln K

Hence,

ΔG° = -RT ln K = -2.303RT log₁₀K

This equation gives the relationship between standard Gibbs energy change for the reaction and its equilibrium constant.

Sample Problems

Problem 1: Determine whether the reaction is spontaneous or non-spontaneous for the given value of ΔH and ΔS. Also, state whether they are exothermic or endothermic.

• ΔH = – 40 kJ and ΔS = +135 JK^-1 at 300K
• ΔH = – 60 kJ and ΔS = -160 JK^-1 at 400K

Solution:

• ΔG = ΔH – T ΔS

 ΔH = – 40 kJ,  ΔS = +135 J K^-1 = 0.135 kJ K^-1 and T = 300K

 ΔG = -40 (kJ) – 0.135(kJ K^-1) × 300(K)

= 80.5 kJ

Because ΔG is negative, the reaction is spontaneous. The negative ΔH value indicates that the reaction is exothermic.

• ΔG = ΔH – T ΔS

ΔH = – 60 kJ,  ΔS = – 160 J K^-1 = – 0.160 kJ K^-1 and T = 400K

 ΔG = -60 (kJ) – 0.160(kJ K^-1) × 400(K)

 = -60 kJ + 64 kJ = 4kJ

The reaction is non-spontaneous because ΔG is positive and exothermic as ΔH is negative.

Problem 2: For a certain reaction ΔH = -25kJ and ΔS = -40J K^-1. At what temperature will it change from spontaneous to non-spontaneous.

Solution;

T = ΔH / ΔS

 ΔH = – 25 kJ,  ΔS = -40 J K^-1  = 0.04 kJ K-1 

Hence, T = -25(kJ) / -0.04 kJ K^-1  = 625K

Because both ΔH and ΔS are negative, the reaction will occur spontaneously at lower temperatures. As a result, the reaction will be spontaneous below 625K and non-spontaneous beyond 625K.

At 625K, the transition from spontaneous to non-spontaneous occurs.

Problem 3: Determine  ΔS_total and decide whether the following reaction is spontaneous at 298K.

ΔH° = -24.8 kJ, ΔS° = 15 J K^-1

Solution: 

The heat evolved in the reaction is 24.8 kJ. The same quantity of heat is absorbed by the surroundings. 

Hence, Entropy change of the surrounding will be,

ΔS_surr = ΔH° / T

= – [(-24.8 (kJ)) / 298 (K)]

= + 83.2 J K^-1

ΔS_total = ΔS_System + ΔS_Surr 

ΔS_Sys = ΔS° = 15 J K^-1

 = 15(J K^-1) + 83.2 (J K^-1)

= 98.2 J K^-1

As ΔS_total is positive, the reaction is spontaneous at 298 K.

Problem 4: Determine whether the reaction,

N₂​O₄ ​(g)⟶2NO₂​ (g)

is spontaneous at 298 K from the following data.

Δ_fH° (N₂O₄) = 9.16 kJ mol^-1, Δ_fH° (NO₂) = 33.2 kJ mol^-1

Solution: 

ΔH=∑Δf​H°(products)−∑Δf​H°(reactants

= 2 × Δ_fH° (NO₂) – Δ_fH° (N₂O₄)

= 2(mol) × 33.2(kJ mol^-1) -1(mol) × 9.16(kJ mol^-1)

= +57.24 kJ

ΔG° = ΔH° – TΔS°

57.24(kJ) – 298(K) × 175.8 × 10^-3 (kJ K^-1)

= +4.85 kJ.

Because ΔG° is positive, the reaction is non-spontaneous at 298 K. 

The temperature at which the reaction changes from spontaneous to non-spontaneous is given by,

T = ΔH° / ΔS°

= 57.24(kJ) / 0.1758(kJ K^-1)

= 325.6 K

Because ΔH° and ΔS° are both positive, the reaction will be spontaneous at high temperature.

The reaction will be spontaneous above 325.6 K.

Problem 5: Determine K_p for the reaction,

2SO₂​(g) + O₂​(g) ⟶ 2SO_3​(g)

is 7.1 × 10²⁴ at 298 K. Calculate ΔG° for the reaction (R = 8.314 JK^-1 mol^-1).

Solution:

ΔG° = -2.303RT log₁₀ K_p

K_p = 7.1 × 10²⁴ 

R = 8.314 JK^-1 mol^-1

T = 298K

Hence,

  ΔG°  = -2.303 × 8.314 × 10^-3 (kJ K^-1 mol^-1) ×  log₁₀ (7.1 ×  10²⁴)

          = -141.8 kJ mol^-1

Problem statement 6: Calculate K_p for the reaction at 513 K,

2NOCl (g) ⟶ 2NO(g) + Cl₂​(g)

with ΔG° = 17.38 kJ mol^-1.

Solution:

ΔG° = -2.303 RT log₁₀ K_p

ΔG° = 17.38 kJ mol^-1

R = 8.314 J K^-1 mol^-1

T = 513K

Hence,

log₁₀ k_p = – ΔG° / 2.303 RT

             = – (17380(J mol^-1) / 2.303 × 8.314 ( J K^-1 mol^-1) × 513(K))

             = -1.769

Hence, K_p = antilog(-1.769)

                = 0.017          

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