Laws Thermodynamics
Laws Thermodynamics
Laws Thermodynamics
Forms of Energy
Energy comes in a variety of forms
Internal
Mechanical
Kinetic
Heat
Potential
Chemical
Electrical
Energy Conservation
The First Law of Thermodynamics states that total energy is conserved for any
thermodynamic system energy can not be created nor destroyed
energy can only change from one form to another
Energy ( E ) constant
Einternal Ekinetic Epotential Emechanical
Eheat Echemical Eelectrical constant
Force
Distance
x
Force
F
p
Area x 2
We can thus define work as:
dW pdV
dW 0
dW 0
if
p
f
pf
pi
Vi
Thermodynamics
Vf
if
dW pdV
f
W pdV
pf
pi
Vi
Thermodynamics
Vf
Joules Law
Vacuum
Air
Valve
Closed
Thermodynamics
Joules Law
Air
Air
Valve
Open
Thermodynamics
Joules Law
Air expanded to fill the container
Change in volume
Change in pressure
No external work was done
Air expanded into a vacuum
within the system
No heat was added or subtract
Thermally insulated system
No change in internal energy
No change in temperature
Air
Air
Valve
Open
dU pdV dQ
dU 0
Thermodynamics
Joules Law
Air expanded to fill the container
Change in volume
Change in pressure
No external work was done
Air expanded into a vacuum
within the system
No heat was added or subtract
Thermally insulated system
No change in internal energy
No change in temperature
Internal Energy is only a function of
temperature
U U(T)
Thermodynamics
Air
Air
Valve
Open
dU pdV dQ
dU 0
dQ
c
dT
Constant Pressure:
Thermodynamics
dQ
cv
dT
dQ
cp
dT
constant volume
Parcel experiences no
change in volume
Parcel experiences no
change in pressure
constant pressure
Starting with:
dQ
cv
dT
If the volume is constant (dV = 0), we can re-write the first law as:
dU pdV dQ
constant volume
dU dQ
dU
cv
dT
Thermodynamics
or
dU c v dT
U c v dT
T1
Also, if we substitute our specific heat equation into the first law:
dU c v dT
dU pdV dQ
dQ c v dT pdV
dQ
cp
dT
dQ c v dT pdV
constant pressure
pV nR *T
dQ c p dT Vdp
Also,
c p c v nR *
Thermodynamics
Concept of Enthalpy
Assume:
Impact:
dW p(V2 - V1 )
2) The systems internal energy increases (U1U2)
dU U 2 - U1
Using the First Law:
dQ U 2 U1 p V2 V1
We can then define Enthalpy (H) as:
H U pV
Thermodynamics
Concept of Enthalpy
Enthalpy:
dQ U 2 U1 p V2 V1
H U pV
dQ dH c p dT
We shall see that Enthalpy will be a useful concept since most sources and
sinks of heating in the atmosphere occur at roughly constant pressure
Thermodynamics
dQ dU dW
dq du dw
dQ dU pdV
dq du pd
dQ c v dT pdV
dq c v dT pd
dQ c p dT Vdp
dq c p dT dp
c p c v nR *
cp cv R d
where:
p = pressure
V = volume
T = temperature
= specific volume
U = internal energy
W = work
Q = heat energy
n = number of moles
Thermal Processes
We will assume that all processes we discuss
are quasi-static they are slow enough that the
system is always in equilibrium.
We also assume they are reversible:
For a process to be reversible, it must be possible to
return both the system and its surroundings to exactly
the same states they were in before the process began.
Thermal Processes
This is an idealized reversible process. The gas
is compressed; the temperature is constant, so
heat leaves the gas. As the gas expands, it
draws heat from the reservoir, returning the gas
and the reservoir to their initial states. The
piston is assumed frictionless.
Thermal Processes
Work done by an expanding gas, constant
pressure:
Thermal Processes
If the volume stays constant, nothing moves and
no work is done.
Thermal Processes
If the temperature is constant, the
pressure varies inversely with the
volume.
Thermal Processes
The work done is the area under the curve:
Thermal Processes
An adiabatic process is one in which no heat
flows into or out of the system. The adiabatic P-V
curve is similar to the isothermal one, but is
steeper. One way to ensure that a process is
adiabatic is to insulate the system.
Thermal Processes
Another way to ensure
that a process is
effectively adiabatic is
to have the volume
change occur very
quickly. In this case,
heat has no time to
flow in or out of the
system.
Thermal Processes
Here is a summary of the different types of
thermal processes:
where
Entropy
A reversible engine has the following relation
between the heat transferred and the reservoir
temperatures:
Rewriting,
Entropy
Entropy
A real engine will operate at a lower efficiency
than a reversible engine; this means that less
heat is converted to work. Therefore,
Entropy
To generalize:
The total entropy of the universe increases whenever
an irreversible process occurs.
The total entropy of the universe is unchanged
whenever a reversible process occurs.
Since all real processes are irreversible, the
entropy of the universe continually increases. If
entropy decreases in a system due to work
being done on it, a greater increase in entropy
occurs outside the system.
Entropy
Summary of
When two objects have the same temperature,
they are in thermal equilibrium.
The first law of thermodynamics is a statement
of energy conservation that includes heat.
Summary
In a reversible process it is possible to return
the system and its surroundings to their initial
states.
Irreversible processes cannot be undone.
The work done during a process is equal to the
area under the curve in the PV plot.
The work done at constant pressure is
The work done at constant volume is zero.
The work done in an isothermal expansion is
Summary
An adiabatic process is one where no heat
transfer occurs.
The value of the specific heat depends on
whether it is at constant pressure or at constant
volume.
Molar specific heat is defined by:
For a monatomic gas at constant volume:
For a monatomic gas at constant pressure:
Summary
In a PV plot,
is constant, where
Summary
A reversible engine has the maximum possible
efficiency,
The maximum possible work:
Summary
Coefficient of performance of a refrigerator:
Summary
Change of entropy during a reversible heat
exchange:
Total entropy of the universe increases whenever an
irreversible process occurs; total entropy is
unchanged after an ideal reversible process.
Entropy is a measure of disorder.
The heat death of the universe will occur when
everything is the same temperature and no more work
can be done.
It is impossible to lower the temperature of an object
to absolute zero in a finite number of steps.
References:
Ball, David W. (2012). Physical Chemistry. 2nd Edition. USA: Cengage Learning.
Winnick, Jack (1997). Chemical Engineering Thermodynamics. Canada: John Wiley and
Sons, Inc.
Smith, J. M., Vanness, H. C., et al. (2005). Introduction to Chemical Engineering. 7th
Edition. Singapore: McGraw-Hill Book. Co.
Kumar, D. S. (2012). Engineering Thermodynamics (Principles and Practices). New Delhi:
S . K. Kataria & Sons.
Moran, Michael J. Shapiro, Howard N., et al. (2011). Principles of Engineering
Thermodynamics. 7th Edition.Canada: Wiley & Sons, Inc.
Senapati, M.(2006). Advanced Engineering Chemistry. Second Edition. New Delhi:
Infinity Science Press LLC.
Perrys ChemicalEnigneers Handbook ( 1997). 7 th Edition. New York: McGraw-Hill Book
Co.