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Thermodynamic Unit 4
Thermodynamic Unit 4
BPS-CSAO1
ALLIED PHYSICS-I (THEORY)
(For B.Sc. Mathematics, Chemistry and Computer Science stadkents
Course Objective:
This paper introduces the students to the busic concepts of Elasticity. Rotational motion, Heat
and thermodynamics, Sound, Optics, Atomic and Nuckat Physics
Learning Outcume:
UNIVERSITY OF MADRAS
U.G. DEGREE COURSES
sVLLABUS WrH EPFECT FROM 2020-202
UNIT V: Opties
Interference-Conditions for Interference Maxima and Minima- Air Wedge- Thickness of A
Thin WireNewton' Rings-Determinat ion of Wavelength Using Newton's Rings
Diffraction-Difference Between Diffraction and Interference-Theory of Transmission Grating
-Normal Incidence-Optical Activity-Biot's Laws -Specific Rotatory Power Determination
of Specific Rotatory Power Using Laurent's Half Shade Polarineter
. Properties of matter, Brijlal and Subeamanyas, Eurasia Publishing co., New Delhi, Ill1
Edition 1983
D.S.Mathur, S.Chand & Company Lad, New Delhi, 10
2. Element of propesties of mater,
Edition 1976
Heat and Thermodynamics, Brijlal &Subramanyam, 5.Chand& Co, 16 Edition 2005
43. Heat and Thermodynamics, D.S. Mattur, Sultan Chand& Som, S Edition 2014
S.Chund and New Delhi, 6 Edaion 2008
Optics and Spectroscopy. R.Murugesha,
co,
5.
6 A text book of Optics, Suhramanyam and Brijlal. S. Chand and co., New Delhi, 22 Edition
2004
7. Optics, Sathya Prakash, Ratan Prakashan Mandhir, New Delhi, VIl Edinion 1990.
o ret tsolbtt bec si CHAPTER 5: Entropy 183
5.10 Entropy of a Steam
Consider 1 gm. of ice at
temperature T. Let us calculate the total
changes into steam at absolute
temperature 7T change in entropy when this ice
If dQ is the amount heat supplied to a
substance at temperature T, the change in
by entropy 1s given
dsdo
T
In order to convert I gm.
of ice at 7, K into water at T K, an amount of heat absorbed is
latent heat of ice, L, say. equal to
AS Clog, noltag v)
This equation gives the total energy of I gm. of steam of
temperature 7, K. For m gm. of sub-
stance, we will multiply eqn. (iv) by m, to give the total change in
entropy during the process. ie., for
converting the ice into steam.
5.9 Entropy of a Perfect Gas
Consider 1 gm. of a perfect gas, occupying a volume Vat pressure P and temperature T. Let dQ
he the heat Supplied to he gas, then according to first law of thermodynamics we have
dQ = dU+ dW
Let Cybe the specific heat at constant volume, dT be the rise of temperature and dV be the change
in volume then
dU =
Cydr and dW= PdV
Substituting in eqn. (), we get
S--Gar PAV)
- J a
..(iid)
We can calculate S in terms of different thermodynamic variables. These are:
Sin terms of temperature and volume
for a perfect gas, P T
reupbaaei
s-J- ulor orzg o s
=
Cy log, T+ r log, V+ constant banliada ei silT doritpo
But r Cp-C, as per Mayer's relation.t 2h vgun
S = Cylog, T+ (Cp-C) log, V+ comstant .iv)
Statistical Physics
182 Heat, Thermodynamics and
-Cyn
-fla+c,4-c-C-)
PV PV
PV=T
-C-G
JGCy
= Cy log, P+ Cp log, V + constant ..(vi)
while deriving the relations for S given by eqns. (ii), iv), (0) and (vi), we have assumed the
entropy of the gas to be zero at absolute zero of temperature
while deriving the relations for S given by eqns. (ii), (iv), (v) and (vi), we have assumed the
entropy of the gas to be zero at absolute zero of temperature.
However, in actual practice, we are intersted in change in entropy of a gas when it goes from its
state of pressure P, volume V, and temperature T, to another state having the values P2, V, and T,
respectively. This is obtained by integrating eqn. (ii) between the limits T and T. The change of
entropy AS=S2-S, for each of the above three cases and can be calculated as under
In terms of temperature and volume, the change of entropy
2
AS=S-S = Cylog+(Cp-C) log, VIl)
AS=S-S, =
C, log7(Cp-C) log, P .VI
The above equations are evaluated for a gas of unit mass. For a gas of m gm., the change
entropy can be obtained by multiplying these relations by mass m of the gas.
5.2 Change in EntropPY
Let us consider reversible Carnot's cycles V
..5.1)
Similarly considering the Carnot's cycle DCEF in which an amount of heat , is absorbed at
constant temperature T, and heat Q3 is rejected at constant temperature 73.
- ..5.2)
COnstant.
In general, if Q is the amount of heat absorbed or rejected at a temperature Tin going from
one adiabatic to the other, then
= Constant
If the two adiabatics are very close to each other and if 8Q is the small quantity of heat absor
at constant temperature T in going from one adiabatic to another, then
Constant
T
et
This constant ratio is called the "change in entropy' between the states represented by
adiabatics. It is denoted by 8S
Yqonin o dge
SA
todolbA nl ygontna nl 9pnorfo
...(5.3)
ture or internal energy and its change between two states is equal to between the states along
any reversible path joining them." dS is an exact differential. Entropy is an extensive property Since t
depends on the mass of the working substance.
Change of Entropy in Reversible Cycle
5.4 Consider a complete reversible Carnot's cycle
ABCD as shown in Fig. 5.2 for an ideal gas formed by
two isothermals i.e. AB at a temperature 7 and CD at
adiabatics BC and DA.
temperature T2 and the two
ds = 0
(tii) Isothermal compression CD: In going from state Cto state D along the isothermal CD, the
working substance rejects heat Q, to the sink at temperature T2. The entropy of the working substanc
decreases and the change in entropy is given by
Jas--92
(iv) Adiabatic compression DA: In going from D to A along the adiabatic DA, there
change in entropy but temperature rises from 7, to T.
15
ds = 0
Thus the net gain in entropy of the working substance in the whole cycle ABCDA
oi J4S+J4s+J4s+as
A
Substituting, we get
ds =0 .(5.5)
where the integral sign wih a circle refers to a
complete cycle.
Thus in a cycle of reversible
process, the entropy of the
constant. In other words, the total change in entropy is alwayssystem
zero.
remains unchanged or remains
4.24 Carnot's Cycle
In order to obtain a continuous supply of work, the working substance is subjected to the follo
w
ng cycle of quasi-static operations known an Carnot's cycle (Fig. 4.16).
.Isothermal expansion. The cylinder is first placed on the source, so that the gas acquie
the temperature T, of the source. It is then allowed to undergo quasi-static expansion. As the a
the perfectly conductin
expands,ichits istemperature tends to fall. Heat passes into the cylinder through
in contact with the source. The gas therefore, undergoes slow isothermal expansion a
base v at
the constant temperature 7
APV)
ISOTHERMAL
T. Q B (P V)010po
(PVA)
D
A
ISOTHERMAL
Ta O2
cPaV)
O H
Fig. 4.16
Let the working substance during isothemal expansion goes from its initial state A (P, V1, 7)to
the state B (P, Vz, 7,) at constant temperature 7, along AB, In this process, the substance absorbs heat
2, from the source at T, and does work W, given by
V ..4.15)
,=W PdV =RT,log,area ABGEA
M
2. Adiabatic expansion. The cylinder is now removed from the source and is placed on the
insulating stand. The gas is allowed to undergo slow adiabatic expansion, performing external wonk
at the expense of its inernal energy, until its temperature falls to 7,, the same as that of the sink
CHAPTER 4: Laws of Thermodynamics 1335
This operation is represented by the adiabatic BC,
starting from the state B (P2, Va) to the state
cP V2). m tnis process, tnre 1s no transfer of heat, the temperature of the substance falls to 12
does
and it some external work Wa given by
W=P.dv K" dV = t b
During adiabatic process, PV = constant = K)
KV-KV
1-Y
-PV
1-Y (:PV=P,V=K)
RT-RT
1-y
This operation is represented by the isothermal CD, starting from the state C (P, V,. T,) to the
state D PV 12). In this process, the substance rejects heat Q, to the sink at T, and work W, is done
on the substance given by
V area CHFDC
RT,loge V, h sooiiget
-ve signe indicates that work is done on the working substance)
4. Adiabatic Compression. The cylinder is now removed from sink and again placed on the
insulating stand. The piston is slowly moved inwards so that the gas is adiabatically compressed and
the temperature rises. The adiabatic compression is continued till the gas comes back to its original
condition i.e. state A (P1, V1, T,), thus completing one full cycle.
This operation is represented by adiabatic DA, starting from D (P. Va. T) to the final state A(P
V, 71). In this process, work W is done on the substance and is given by
W= P.dv
-CYLINDER
WORKING SUBSTANCE
SOURCE SINK
STAND
AtT At T2
Fig. 4.15
1. A cylinder having perfectly non-conducting walls, a perfectly conducting base and is pre-
-0
7-T)(SS)
T-5)
ni 7-T
T
= 1-2 5.1
T