Eee/Ete 132 Introduction To Materials and Chemistry: Thermodynamics and Enthalpy For Engineers
Eee/Ete 132 Introduction To Materials and Chemistry: Thermodynamics and Enthalpy For Engineers
CHEMISTRY
Pressure
The State Diagram – Inside Steam Turbine
• Processes1-2, 2-3, and 3-4
represents a typical constant
pressure heating of water which
initially heated to its boiling
point,(1-2),upon continued heat
input it starts to evaporate at point
2, it is completely liquid,
• Then gradually some of the water
becomes vapour till it reaches
point3, where all the water has
evaporated, further heating will
make the water vapour
superheated(process 3-4).
Worked Example
• A 6 meter cube tank contains helium at 400K is evacuated form
atmospheric pressure of 100kPa to a final pressure of 2.5kPa.
• Determine
a) the mass of helium remaining in the tank;
b) the mass of helium pumped out;
c) if the temperature of the remaining helium falls to 10oC, what is the pressure in kPa?
Home Task
• A biker equips his bike tyres with a relief-type valve so that the
pressure inside the tyre will never exceed 220 kPa (gauge). One day he
takes a trip with a pressure of 200 kPa (gauge) and a temperature of
23°C in the tyres. After a long time the temperature of the air in the
tyre reaches 83° C. If each tyre consists of 0.11 kg air. Determine:
∆U = Q - W
The first law makes use of the key concepts of internal energy (DU), heat (Q), and system work
(W).
2. Internal Energy
Internal energy is defined as the energy associated with the random, disordered motion
of molecules. It is separated in scale from the macroscopic ordered energy associated
with moving objects; it refers to the invisible microscopic energy on the atomic and
molecular scale.
During a non flow process the change in internal energy is calculated assuming the
closed system volume remains constant, the following equation is used
∆U = mCv ∆T
3. System Work
Work performed on or by the working fluid within a system’s boundary is defined as the
summation (or integration) of the product of pressure and volume of the fluid during a process.
W = ∫P.dV
A. For a constant pressure process, the work during an isobaric process is
simply :
W = p (V2 - V1)
B. For a constant volume process, dv =0; hence the work during an
isochoric process is simply :
W =0
C. For a constant temperature ,isothermal process,
PV = C
D. For an adiabatic ( polytropic ) process,
PV ᶯ = c
integrating between states 1 and 2, the work done is derived :
and using the ideal gas definition, the work done can be written in terms of intial and
final states temperatures:
Second Law of Thermodynamics
• The second law, indicates that, although the net heat supplied,Q1-Q2, in a cycle is equal
to the network done, W, the gross heat supplied, Q1 must be greater than the network
done; some heat must always be rejected by the system.
Q1 > W,
or to be precise:-
• W = Q1 – Q2
• Where, Q1 is the heat supplied and Q2 is the heat rejected.
The ratio of network output to heat supplied is known as the thermal efficiency of the
system.
In 1865 Clausius observed that the amount dQ/T is proper to describe the
thermodynamic phenomenon. This amount was named reduced heat or entropy.
During a process, the change in entropy is defined as :
• dS = Q/T
Definitions of Entropy :
• But q = Cv dT
• Hence du = CvdT
Or Cv = du/dT
Specific Heat at Constant Pressure Cp
• Consider a constant pressure non-flow process, the first law:- q – w = du
• For a constant pressure process
or Cp = dh/dT
Relationship Between Specific Heats
• Since
H = U + PV
dH = dU + d(PV) ;
d(PV) = d(mRT) = mRdT
m Cp dT = m Cv dT + m R dT
• Therefore, Cp = Cv + R Ie Cp > Cv
• The ratio Cp/Cv = n is called the adiabatic index.
• The reason for the differences between Cp and Cv is that in the constant
pressure process part of the heat transferred is used in doing work against the
moving system boundary and all heat therefore is not available for raising the
gas temperature.
• The First Law of Thermodynamics:-
Q – W = ΔU
• And the Second Law of Thermodynamics:-
Q = Tds
This can also be written in terms of volumes and pressures as:-
Third Law
• The entropy of a perfect crystal is zero when the temperature of a the
crystal is equal to absolute zero (0 K).
• At 0 K, there is no thermal motion, and if the crystal is perfect, there
will be no disorder
• Once the temperature begins to rise above 0, the particles begin to
move and entropy gradually increases as the average kinetic energy of
the particles increases.
• When temperature reaches the melting point of the substance (Tm),
there is an abrupt increase in entropy as the substance changes from a
solid to a more disordered liquid.
Example 3
A closed rigid container has a volume of 1 m³ and holds air at
345 kPa and 20°C. Heat is added until the temperature is
327°C. Determine the change in Internal Energy:-
a) Using an average value of the specific heat.
b) Taking into account the variation of specific
heat with temperature.
Example 4
Air at 27°C receives heat at constant volume until its
temperature reaches 927oC. Determine the heat added per
kilogram? Assume for air CV = 0.718 kJ/kgK.
Example 5
• An insulated, constant-volume system
containing 1.36 kg of air receives 53 kJ of
paddle work. The initial temperature is
27oC. Determine
• the change of internal energy.
• the final temperature.
Assume a mean value Cv = 0.718 kJ/kgK
Project Discussions
• Literature Review/ Project Report ( 10 %)
• Project Viva/ presentation ( 5 %)
Next Class
• Quiz on
• Lectures 1, 2, 3, 4&5
• Short Questions, MCQ, Broad Questions