MIT OpenCourseWare

http://ocw.mit.edu

5.60 Thermodynamics & Kinetics

Spring 2008

For information about citing these materials or our Terms of Use, visit: http://ocw.mit.edu/terms.
5.60 Spring 2008 Lecture #2 page 1

Work, Heat, and the First Law

• Work: w = F ⋅A

applied force distance

A
pext
Expansion work
pext

F = pext A

w = − ( pext A ) A = − pext ∆V

convention: Having a “-“ sign here implies w > 0 if ∆V < 0 , that

is, positive work means that the surroundings do
work to the system. If the system does work on the
surroundings ( ∆V > 0 ) then w < 0 .

If pext is not constant, then we have to look at infinitesimal changes

d-w = − pext dV d- means this is not an exact differential

w = −∫1 pext dV
2
Integral depends on the path!!!

• Path dependence of w

Example: assume a reversible process so that pext = p

Ar (g, p1, V1) = Ar (g, p2, V2)

Compression V1 > V2 and p1 < p2

 5.60 Spring 2008 Lecture #2 page 2

p ext= p 1

p ext= p 2
p 1,V1 c ompression
p 2,V2

initial final

Two paths:
(1) First V1 → V2 at p = p1 (2) First p1 → p2 at V = V1
then p1 → p2 at V = V2 then V1 → V2 at p = p2

Ar(g, p1, V1) = Ar(g, p1, V2) = Ar(g, p2, V2) Ar(g, p1, V1) = Ar(g, p2, V1) = Ar(g, p2, V2)

p
p2
final
(2)

p1 init.
(1)

V2 V1

w(1) = −∫V pext dV − ∫V p ext dV w(2) = − ∫V pext dV − ∫V pext dV

V2 V2 V1 V2

1 2 1 1

= −∫V p1dV = − p1 (V2 −V1 ) = −∫V p2dV = − p2 (V2 −V1 )

V2 V2

1 1

w(1) = p1 (V1 − V2 ) w(2) = p2 (V1 −V2 )

(Note w > 0, work done to system to compress it)

w(1) ≠ w(2) !!!

Note for the closed cycle [path (1)] - [path (2)], ∫ d-w ≠ 0
closed cycle
w is not a state function cannot write w = f(p,V)
5.60 Spring 2008 Lecture #2 page 3

WORK
Work (w) is not a function of state.

For a cyclic process, it is possible for ∫ d-w ≠ 0

state 1 state 2

HEAT
That quantity flowing between the system and the
surroundings that can be used to change the temperature
of the system and/or the surroundings.

Sign convention: If heat enters the system, then it is

positive.

Heat (q), like w, is a function of path. Not a state function

It is possible to have a change of state

(p 1 , V 1 , T 1 ) = (p 2 , V 2 , T 2 )

adiabatically (without heat transferred)

or nonadiabatically.

Historically measured in calories

[1 cal = heat needed to raise 1 g H2O 1°C,
from 14.5°C to 15.5°C]

The modern unit of heat (and work) is the Joule.

1 cal = 4.184 J
5.60 Spring 2008 Lecture #2 page 4

Heat Capacity C - connects heat with temperature

⎛ đq ⎞
đq = CpathdT or C path = ⎜ ⎟
⎝ dT ⎠ path

heat capacity is path dependent

Constant volume: CV
Constant volume: Cp

∴ q= ∫ C pathdT
path

Equivalence of work and heat [Joule (1840’s)]

Joule showed that it’s possible to raise the temperature of H2O

(a) with only heat T1 → T2

(b) with only work T1 → T2

(weight falls &
churns propeller)
5.60 Spring 2008 Lecture #2 page 5

Experimentally it was found that

∫ (d-w +d-q ) = 0
⇒ The sum (w + q) is independent of path

⇒ This implies that there is a state function whose differential is

đw + đq

We define it as U, the “internal energy” or just “energy”

∴ dU = đw + đq

For a cyclic process

∫ dU = 0

For a change from state 1 to state 2,

2
∆U = ∫ dU = U2 − U1 = q + w does not depend on path

each depends on path individually, but not the sum

For fixed n, we just need to know 2 properties, e.g. (T, V), to fully
describe the system.

So U = U (T ,V ) )

U is an extensive function (scales with system size).

U
U = is molar energy (intensive function)
n
5.60 Spring 2008 Lecture #2 page 6

THE FIRST LAW

dU = d-q +d-w
or
Mathematical statement: ∆U = q + w
or
− ∫ d-q = ∫ d-w

Corollary: Conservation of energy

∆Usystem = q + w ∆Usurroundings = −q − w

⇒ ∆Uuniverse = ∆Usystem + ∆Usurroundings = 0

Clausius statement of 1st Law:

The energy of the universe is conserved.