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Page 1: Equilibrium and Kinetics

Equilibrium and Kinetics

Chapter 2

Page 2: Equilibrium and Kinetics

In the last lecture we used the mechanicalAnalogy to understand the concept ofStability and metastability

Recap

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metastable

unstable

stable

Activation barrier

Fig. 2.2Recap

P.E

Configuration

Mechanical push to overcome activation barrier

System automaticallyattains the stable state

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Recap

If we want to transform the Local Minimum - METASTABLE to Global Minimum - Most STABLE then we have to overcome the activation barrier (could be by mechanical push, thermal activation)

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Thermodynamic functions

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U = internal energy

Courtsey: H. Bhadhesia

At constant pressure

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Courtsey: H. Bhadhesia

This expression can also be expressed as: U = Uo + dtCt

o

v

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Sum of internal energy and external energy

For solids and liquid the PV term is negligible

Courtsey: H. Bhadhesia

dtCt

o

pThe above expression can also be expressed as: H = Ho +

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Courtsey: H. Bhadhesia

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P

Courtsey: H. Bhadhesia

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Entropy

Courtsey: H. Bhadhesia

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Courtsey: H. Bhadhesia

How do you measure the entropy?

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Gibbs Free Energy

TSHG

Condition for equilibrium

≡ minimization of G

Local minimum ≡ metastable equilibrium

Global minimum ≡ stable equilibrium

(2.6)

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G = GfinalGinitial

G = 0 reversible change

G < 0 irreversible or spontaneous change

G > 0 impossible

(2.7)

(2.8)

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The variation of G with temperature

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Atomic

or

statistical

interpretation of entropy

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The entropy of a system can be defined by two components:

Thermal:

Configurational: WkS ln

Entropy

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Boltzmann’s Epitaph

WkS lnW is the number of microstates corresponding to a given macrostate

(2.5)

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N=16, n=8, W=12,870

)!(!

!

nNn

NCW n

N

(2.9)

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Stirling’s Approximation

nnnn ln!ln(2.11)

If n>>>1

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WkS ln

)!(!

!ln

nNn

Nk

)]ln()(lnln[ nNnNnnNNk

(2.10)

(2.12)

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KINETICS: Arrhenius equationSvante Augustus

Arrhenius

1859-1927

Nobel 1903

RT

QArate exp

(2.15)

Rate of a chemical reaction varies with temperature

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R

Qslope

RT

QArate exp

ln (rate)

T

1

Fig. 2.4

Arrhenius plot

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Thermal energy

Average thermal energy per atom per mode of oscillation is kT

Average thermal energy per mole of atoms per mode of oscillation is NkT=RT

(2.13)

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Maxwell-Boltzmann Distribution

kT

E

N

nexp

Fraction of atoms having an energy E

at temperature T

(2.14)