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Lecture 3 Clausius Inequality

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244 views

Lecture 3 Clausius Inequality

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Bhuwanesh Kumar
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© Attribution Non-Commercial (BY-NC)
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Lecture 3

Clausius Inequality

CY1001 2010 T. Pradeep


Assume reversible and irreversible paths between two states.
Reversible path produces more work.
dU is the same for both the paths.

dU = dq + dw = dqrev + dwrev

dqrev – dq = dw - dwrev ≥ 0

dqrev/T ≥ dq/T

dS ≥ dq/T Clausius inequality

System is isolated.

dS ≥ 0 Clausius inequality
Equilibrium

Entropy

Process
Spontaneous processes entropy
increases.

“Entropy is Time’s Arrow”

Arthur Stanley Eddington (1882-1944)


How do we derive conditions for
equilibrium and spontaneity?

For an isolated system


∆S ≥ 0, > sign for a spontaneous process and = for equilibrium.

In the case of open or closed system, there are two ways

1. Evaluate ∆S for systems and surroundings.


∆Stotal =∆Ssystem + ∆Ssurroundings

∆S ≥ 0
2. Other way is to define entropy change of the system alone.

dStotal = dSsystem + dSsurroundings

dS - dq/T ≥ 0 Clausius inequality

Consider constant volume:


dS - dU/T ≥ 0
TdS ≥ dU (constant V and so no work due to expansion)

At constant U or at constant S, the expression is:

1. dSU,V ≥ 0 2. dUS,V ≤ 0

Criterion of spontaneity 1. is the common statement of second law.


2. Entropy is unchanged, for sponteneity, entropy of the surroundings must
increase for which U of the system as to decrease.
At constant pressure,
TdS ≥ dH
dA = dU – TdS
dG = dH – TdS
1. dSH,P ≥ 0 2. dHS,P ≤ 0

Interpretations are the same. (dA)T, V ≤ 0


(dG)T, P ≤ 0
The inequalities mean,
dU – TdS ≤ 0
dH – TdS ≤ 0

We define,
A = U – TS Helmoltz energy
G = H – TS Gibbs energy
Hermann von Helmholtz
Born: 31 Aug 1821 in Potsdam, Germany
Died: 8 Sept 1894 in Berlin, Germany
What is A?

dU = dq + dW – First law
TdS ≥ dq

dU ≤ TdS + dW

dW ≥ dU-TdS = dA

Most negative value of W is Wmax and that is equal to dA.

Under constant T and V can the system do


work?
A is not defined only for this condition!!
G = H – TS H = U + PV dH = dq + dw + d(PV)
= U + PV – TS
dG = dH + – TdS – SdT
= dq + dw + d(PV) – TdS – SdT
At constant temperature,
= TdS + dwrev + d(PV) – TdS = dwrev + d(PV)
dw rev = -PdV + dwadditional
dG = dw rev + d(PV) = -PdV + dwadditional + PdV – VdP
dG = dwadditional – VdP Work function
At constant P and T, Free energy
dG = dwadditional Carnot limitation

Decrease in free energy, ∆G, at constant temperature and


pressure corresponds to the maximum work other than the P – V work that the system is capable
of doing under reversible conditions.
Conditions of equilibrium

(dS)U, q ≥ 0
(TdS)U, V ≥ 0
(dA)T, V ≤ 0
(dG)T, P ≤ 0
If there is other work in addition to P – V work,
TdSsystem – [dUsystem + PdVsystem + dwother] ≥ 0
Combined law
Now conditions for spontaneity and equilibrium can be
found out by subjecting it to various conditions.
G is a function of P and T
G = f(P, T)
dG = (∂G/∂P)T dp + (∂G/∂T)P dT 1
G = H – TS
= U + PV – TS
dG = dU + PdV + VdP – TdS – SdT
dU = TdS – PdV
dG = VdP – SdT 2
Comparing 1 and 2
(∂G/∂P)T = V
(∂G/∂T)P = –S One component system
Variation of G with T
Gas

G Solid

Liquid

T
(∂G/ ∂T)P = -S
Variation of G with P
Gas

G
Liquid

Solid

P
(∂G/ ∂P)T = V
S and V are always positive quantities. G should increase
with P at constant temperature and decrease with temperature at
constant pressure. For a finite change in free energy at constant
temperature,
∫P2P1 dG = ∫P2P1VdP

For solids and liquids, the volume change will be small and
∆G = V∆P Gm o
Such changes in free energy are very small.
For gases, since volume change is large, ∆G is large.
∫21 dG = ∫21 nRT/P dP
= nRT ln P2/P1
This relation shows that G is (1) extensive and (2) a state -Infinity
Po
function. ∆G for a change 1 → 2 is the same whether the change of
state is carried out reversibly or irreversibly.

Gm(P) = Gom + RT ln P/Po


Gibb’s Helmoholtz equation
∆Gf° values predict the feasibility of a reaction at 298 K.
∆G values at any temperature can be calculated by
Gibbs - Helmholtz equation.
∆G = ∆H − T∆S
(∂G/∂T)P = −S
(∂∆G/∂T)P = −∆S
∆G = ∆H + T (∂∆G/∂T)P (1)
∆G can be evaluated from emf measurement since ∆G = −nFE
Where n = number of electrons evaluated, F = Faraday,
E = potential of the cell. F= 96500 Coulombs/gm. equiv.
Divide eqn. 1 by –T2
−∆G/T2 + 1/T (∂∆G/∂T)P = −∆H/T2
Write −1/T2 as ∂/∂T (1/T)
∆G [∂/∂T (1/T)]P +1/T (∂∆G/∂T)P = −∆H/T2

{UdV + VdU = d(UV)}

[∂/∂T (∆G/T)]P = −∆H/T2


Helmholtz equation:

[∂/∂T (∆A/T)]P = −∆U/T2]

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