Lecture1 Introduction PDF
Lecture1 Introduction PDF
Arti Dua
Department of Chemistry
IIT Madras
!
Lecture 1: Introduction
to Thermodynamics
Thermodynamics: Introduction
! dG = dH - TdS
Heat Work
Z T2
dT = T = (T2 T1 )
T1
State Function
T1 T2
State Function
If T(x, y) is a state function such that the function and their derivatives are
continuous and single valued then
@ 2 T (x, y) @ 2 T (x, y)
=
@x@y @y@x
State functions are exact
differentials
@ 2 F (x, y) @ 2 F (x, y)
6=
@y@x @x@y
Work and heat are path functions. They depend on how the
thermodynamic system changes from the initial to final state
Z
dw 6= w
Z
dq 6= q
Path Functions
Work
Work of expansion
l
convention
Reversible vs. Irreversible Processes
p
p
Compression
Cyclic Transformation
Irreversible
Total work in single stage
expansion and compression:
Reversible:
Adiabatic:
The first law of thermodynamics
For fixed n we only need to know two properties (T,V) to describe the system
Constant Volume:
✓ ◆ ✓ ◆ ✓ ◆
@U @T @V
U (T, V ) =) = 1
@T V @V U @U T
Cyclic relation
✓ ◆ ✓ ◆ ✓ ◆
@U @U @T
=
@V T @T V @V U
CV ⌘J Joule Coefficient
dU = CV dT CV ⌘J dV
⌘J = 0 (ideal gases) =) U (T )
Chemical reactions usually take place at constant pressure. Enthalpy is a useful function of
state under these condition H(T, p).
The change in the enthalpy of a system is equal to the amount of heat exchanged by the
system at constant pressure.
✓ ◆ ✓ ◆
@H @H
H(T, p) =) dH = dT + dp
@T p @p T
Cp what is this?
✓ ◆ ✓ ◆ ✓ ◆
@H @T @p
H(T, p) =) = 1
@T p @p U @H T
✓ ◆ ✓ ◆ ✓ ◆
@H @H @T
=
@p T @T p @p U
Joule-Thomson experiment
estimates this quantity
dH = Cp dT + Cp µJT dp
Isothermal
work
A Thermodynamic cycle (Homework)