Thermodynamics
Thermodynamics
Thermodynamics
Thermodynamics
GATE, IES & IAS 20 Years Question Answers
Contents
Chapter – 1: Basic Concepts
Chapter - 4 : Entropy
Er. S K Mondal
IES Officer (Railway), GATE topper, NTPC ET-2003 batch, 12 years teaching
experienced, Author of Hydro Power Familiarization (NTPC Ltd)
Page 1 of 121
Note
If you think there should be a change in
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mail at [email protected]
I will send you complete explanation.
Every effort has been made to see that there are no errors (typographical or otherwise) in the
material presented. However, it is still possible that there are a few errors (serious or
otherwise). I would be thankful to the readers if they are brought to my attention at the
following e-mail address: [email protected]
S K Mondal
Page 2 of 121
Basic Concepts
S K Mondal’s Chapter 1
1. Basic Concepts
Quasi-Static Process
GATE-3. A frictionless piston-cylinder device contains a gas initially at 0.8 MPa and
0.015 m3. It expands quasi-statically at constant temperature to a final volume
of 0.030 m3. The work output (in kJ/kg) during this process will be: [GATE-2009]
(a) 8.32 (b) 12.00 (c) 554.67 (d) 8320.00
Page 3 of 121
Basic Concepts
S K Mondal’s Chapter 1
(c) Both internal energy and enthalpy of the gas remain constant
(d) Both internal energy and enthalpy of the gas increase
GATE-5. Air is compressed adiabatically in a steady flow process with negligible change
in potential and kinetic energy. The Work done in the process is given by:
[GATE-1996, IAS-2000]
(a) –∫Pdv (b) +∫Pdv (c) –∫vdp (d) +∫vdp
GATE-8. For reversible adiabatic compression in a steady flow process, the work
transfer per unit mass is: [GATE-1996]
(a ) ∫ pdv (b) ∫ vdp (c) ∫ Tds (d ) ∫ sdT
Page 4 of 121
Basic Concepts
S K Mondal’s Chapter 1
IES-3. Which one of the following is the extensive property of a thermodynamic
system? [IES-1999]
(a) Volume (b) Pressure (c) Temperature (d) Density
IES-4. Consider the following properties: [IES-2009]
1. Entropy 2. Viscosity
3. Temperature 4. Specific heat at constant volume
Which of the above properties of a system is/are extensive?
(a) 1 only (b) 1 and 2 only (c) 2, 3 and 4 (d) 1, 2 and 4
Page 5 of 121
Basic Concepts
S K Mondal’s Chapter 1
(c) A is true but R is false
(d) A is false but R is true
IES-10. Ice kept in a well insulated thermo flask is an example of which system?
(a) Closed system (b) Isolated systems [IES-2009]
(c) Open system (d) Non-flow adiabatic system
water
(b) 1/273.15th of the normal freezing point of water
(c) 100 times the difference between the triple point of water and the normal freezing
point of water
(d) 1/273.15th of the triple point of water
IES-15. In a new temperature scale say °ρ, the boiling and freezing points of water at
one atmosphere are 100°ρ and 300°ρ respectively. Correlate this scale with the
Centigrade scale. The reading of 0°ρ on the Centigrade scale is: [IES-2001]
(a) 0°C (b) 50°C (c) 100°C (d) 150°C
Page 6 of 121
Basic Concepts
S K Mondal’s Chapter 1
IES-16. Assertion (a): If an alcohol and a mercury thermometer read exactly 0°C at the
ice point and 100°C at the steam point and the distance between the two points
is divided into 100 equal parts in both thermometers, the two thermometers
will give exactly the same reading at 50°C. [IES-1995]
Reason (R): Temperature scales are arbitrary.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IES-17. Match List-I (Type of Thermometer) with List-II (Thermometric Property) and
select the correct answer using the code given below the [IES 2007]
List-I List-II
A. Mercury-in-glass 1. Pressure
B. Thermocouple 2. Electrical resistant
C. Thermistor 3. Volume
D. Constant volume gas 4. Induced electric voltage
Codes: A B C D A B C D
(a) 1 4 2 3 (b) 3 2 4 1
(c) 1 2 4 3 (d) 3 4 2 1
Page 7 of 121
Basic Concepts
S K Mondal’s Chapter 1
A. Throttling process 1. No work done
B. Isentropic process 2. No change in entropy
C. Free expansion 3. Constant internal energy
D. Isothermal process 4. Constant enthalpy
Codes: A B C D A B C D
(a) 4 2 1 3 (b) 1 2 4 3
(c) 4 3 1 2 (d) 1 3 4 2
IES-22. The heat transfer, Q, the work done W and the change in internal energy U are
all zero in the case of [IES-1996]
(a) A rigid vessel containing steam at 150°C left in the atmosphere which is at 25°C.
(b) 1 kg of gas contained in an insulated cylinder expanding as the piston moves slowly
outwards.
(c) A rigid vessel containing ammonia gas connected through a valve to an evacuated
rigid vessel, the vessel, the valve and the connecting pipes being well insulated and
the valve being opened and after a time, conditions through the two vessels becoming
uniform.
(d) 1 kg of air flowing adiabatically from the atmosphere into a previously evacuated
bottle.
[IES-2006]
(a) A – B – C (b) B – A – C (c) A – C – B (d) C – A – B
Page 8 of 121
Basic Concepts
S K Mondal’s Chapter 1
IES-25. An ideal gas undergoes an
isothermal expansion from
state R to state S in a turbine
as shown in the diagram given
below:
The area of shaded region is
1000 Nm. What is the amount is
turbine work done during the
process?
(a) 14,000 Nm (b) 12,000 Nm
(c) 11,000 Nm (d) 10,000 Nm [IES-2004]
IES-26. Assertion (A): The area 'under' curve on pv plane, ∫ pdv represents the work of
reversible non-flow process. [IES-1992]
Reason (R): The area 'under' the curve T–s plane ∫ Tds represents heat of any
reversible process.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IES-27. If ∫ pdv ∫
and − vdp for a thermodynamic system of an Ideal gas on valuation
give same quantity (positive/negative) during a process, then the process
undergone by the system is: [IES-2003]
IES-28. Which one of the following expresses the reversible work done by the system
(steady flow) between states 1 and 2? [IES-2008]
2 2 2 2
(a) ∫ pdv
1
(b) − ∫ vdp
1
(c) − ∫ pdv
1
(d) ∫ vdp
1
Page 9 of 121
Basic Concepts
S K Mondal’s Chapter 1
Page 10 of 121
Basic Concepts
S K Mondal’s Chapter 1
IAS-9. For the expression ∫ pdv to represent the work, which of the following
conditions should apply? [IAS-2002]
(a) The system is closed one and process takes place in non-flow system
(b) The process is non-quasi static
(c) The boundary of the system should not move in order that work may be transferred
(d) If the system is open one, it should be non-reversible
IAS-10. Air is compressed adiabatically in a steady flow process with negligible change
in potential and kinetic energy. The Work done in the process is given by:
[IAS-2000, GATE-1996]
(a) –∫pdv (b) +∫pdv (c) –∫vdp (d) +∫vdp
Page 11 of 121
Basic Concepts
S K Mondal’s Chapter 1
IAS-11. Match List-I with List-II and select the correct answer using the codes given
below the lists: [IAS-2004]
List-I List-II
A. Bottle filling of gas 1. Absolute Zero Temperature
B. Nernst simon Statement 2. Variable flow
C. Joule Thomson Effect 3. Quasi-Static Path
D. ∫pdv 4. Isentropic Process
5. Dissipative Effect
6. Low grade energy
7. Process and temperature during phase
change.
Codes: A B C D A B C D
(a) 6 5 4 3 (b) 2 1 4 3
(c) 2 5 7 4 (d) 6 1 7 4
Page 12 of 121
Basic Concepts
S K Mondal’s Chapter 1
∫
GATE-5. Ans. (c) For closed system W = + pdv , for steady flow W = − vdp ∫
GATE-6. (c)
GATE-7. Ans. (b) W = Resistance pressure. Δ V = 1 × Δ V = 100 × 0.1 kJ = 1kJ
GATE-8. Ans. (b) W = − ∫ vdp
Page 13 of 121
Basic Concepts
S K Mondal’s Chapter 1
• But remember 100% heat can’t be convertible to work but 100% work can be
converted to heat. It depends on second law of thermodynamics.
• A thermodynamic system is defined as a definite quantity of matter or a region in
space upon which attention is focused in the analysis of a problem.
• The system is a macroscopically identifiable collection of matter on which we focus
our attention
IES-6. Ans. (b) In closed thermodynamic system, there is no mass transfer but energy transfer
exists.
IES-7. Ans. (b)
IES-8. Ans. (d) Isentropic means reversible adiabatic. Heat transfer in any finite temp difference is
irreversible.
IES-9. Ans. (a) The energy transfer as heat and work during the forward process as always
identically equal to the energy transfer is heat and work during the reversal or the
process is the correct reason for maximum efficiency because it is conservative system.
IES-10. Ans. (b) Isolated System - in which there is no interaction between system and the
surroundings. It is of fixed mass and energy, and hence there is no mass and energy
transfer across the system boundary.
IES-11. Ans. (a) All temperature measurements are based on Zeroth law of thermodynamics.
IES-12. Ans. (a) Entropy - related to second law of thermodynamics.
Internal Energy (u) = f (T) only (for an ideal gas)
Van der Wall's equation related to => real gas.
IES-13. Ans. (d)
IES-14. Ans. (d)
0 − 300 C −0
IES-15.Ans. (d) = ⇒ C = 150°C
100 − 300 100 − 0
IES-16. Ans. (b) Both A and R are correct but R is not correct explanation for A. Temperature is
independent of thermometric property of fluid.
IES-17. Ans. (d)
IES-18. Ans. (d) But it will occur at absolute zero temperature.
IES-19. Ans. (c) Time Constants: The time constant is the amount of time required for a
thermocouple to indicated 63.2% of step change in temperature of a surrounding media.
Some of the factors influencing the measured time constant are sheath wall thickness,
degree of insulation compaction, and distance of junction from the welded cap on an
ungrounded thermocouple. In addition, the velocity of a gas past the thermocouple probe
greatly influences the time constant measurement. In general, time constants for
measurement of gas can be estimated to be ten times as long as those for measurement
of liquid. The time constant also varies inversely proportional to the square root of the
velocity of the media.
IES-20. Ans. (c)
IES-21. Ans. (a)
IES-22. Ans. (c) In example of (c), it is a case of free expansion heat transfer, work done, and
changes in internal energy are all zero.
Page 14 of 121
Basic Concepts
S K Mondal’s Chapter 1
⎛m m⎞
IES-23. Ans. (a) Work done (W) = P Δ V = 100 × (V2 – V1) = 100 × ⎜ − ⎟
⎝ ρ2 ρ1 ⎠
⎛ 1 1 ⎞
= 100 kPa × ⎜ − ⎟ = –9.1 J
⎝ 999 916 ⎠
IES-24. Ans. (d) WA = ∫ pdV = 4 × (2 − 1) = 4 kJ
1
WB = ∫ pdV = × 3 × (7 − 4) = 4.5 kJ
2
WC = ∫ pdV = 1× (12 − 9) = 3kJ
IES-25. Ans. (c) Turbine work = area under curve R–S
= ∫ pdv = 1 bar × ( 0.2 − 0.1 ) m3 + 1000 Nm
= 105 × ( 0.2 − 0.1 ) Nm + 1000Nm = 11000 Nm
IES-26. Ans. (b)
IES-27. Ans. (d) Isothermal work is minimum of any process.
pv = mRT
pdv + vdp = 0[ ∵ T is constant]
∫ pdv = − ∫ vdp
2
IES-28. Ans. (b) For steady flow process, reversible work given by − vdp .∫
1
IES-29. Ans. (c) A is true because change in heat and work are path functions and thus can't be
expressed simply as difference between the end states. R is false because both work and
heat are inexact differentials.
∫
IAS-10. Ans. (c) For closed system W = + pdv , for steady flow W = − vdp ∫
Page 15 of 121
Basic Concepts
S K Mondal’s Chapter 1
IAS-12. Ans. (b) Start with D. ∫PdV only valid for quasi-static path so choice (c) & (d) out.
Automatically C-4 then eye on A and B. Bottle filling of gas is variable flow so A-2.
IAS-13. Ans. (c) W = ∫ pdv where pressure (p) is an intensive property and volume (v) is an
extensive property
IAS-14. Ans. (a) Pressure is intensive property but such option is not there.
Page 16 of 121
Fir
rst Law
w of Therm
T odyna
amics
S K Mo
ondal’s
s Chaapter 2
2. Firstt Law
w of T herm
modyn
namic
cs
ASKED
D OBJEC
CTIVE QUESTIONS (G
GATE, IES, IAS)
P
Previou
us 20-Y
Years GATE
E Ques
stions
A
Applicatiion of First
F Law
w to Ste
eady Flo
ow Proc
cess S.F
F.E.E
Co
ommon Data for Qu
uestions Q1
Q and Q2
2: [GA
ATE-2009]
Th
he inlet and
d the outle
et conditions of
ste
eam for an
n adiabatic
c steam tur
rbine
are as indic
cated in the
t figure. The
no
otations are as usually followed.
ATE-1.
GA If mass
m flow rate
r of steam through the turbine is 20 kg/ss the power
r output of
thee turbine (in
n MW) is: [GA
ATE-2009]
(a) 12.157 (b) 12.941 (cc) 168.001 (d) 168.785
GA
ATE-2. Asssume the abbove turbin ne to be parrt of a simpple Rankine e cycle. The density of
water at the inlet to the e pump is 1000 kg/m . Ignoring kinetic
3 k andd potential
eneergy effects
s, the specifi
fic work (in kJ/kg) supp plied to the pump is:
[G
GATE-2009]
(a) 0.293 (b) 0.35 1 (c)) 2.930 (d) 3.510
3
GA
ATE-3. The
e following
g four figures have been dra awn to re
epresent a fictitious
the
ermodynammic cycle, on
n the p-v and
d T-s planess. [G
GATE-2005]
Page 17 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
According to the first law of thermodynamics, equal areas are enclosed by
(a) Figures 1and 2 (b) Figures 1and 3 (c) Figures 1and 4 (d) Figures 2 and 3
IES-2. Two blocks which are at different states are brought into contact with each
other and allowed to reach a final state of thermal equilibrium. The final
temperature attained is specified by the [IES-1998]
(a) Zeroth law of thermodynamics (b) First law of thermodynamics
(c) Second law of thermodynamics (d) Third law of thermodynamics
Page 18 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
IES-3. For a closed system, the difference between the heat added to the system and
the work done by the system is equal to the change in [IES-1992]
(a) Enthalpy (b) Entropy
(c) Temperature (d) Internal energy
(c)1 − γ
( v3 − v1 ) p1 (b) 1 −
1 ( v3 − v1 ) p1
( p2 − p1 ) v1 γ ( p2 − p1 ) v1
[IES-1998]
IES-6. A closed system undergoes a process 1-2 for which the values of Q1-2 and W1-2 are
+20 kJ and +50 kJ, respectively. If the system is returned to state, 1, and Q2-1 is -
10 kJ, what is the value of the work W2-1? [IES-2005]
(a) + 20 kJ (b) –40 kJ (c) –80 kJ (d) +40 kJ
Page 19 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
Process Q kJ/min W kJ/min
A–B +687 +474
B–C -269 0
C–D -199 -180
D–A +75 0
The power developed in kW is, nearly,
(a) 4.9 (b) 24.5 (c) 49 (d) 98
IES-11. The values of heat transfer and work transfer for four processes of a
thermodynamic cycle are given below: [IES-1994]
Process Heat Transfer (kJ) Work Transfer (kJ)
1 300 300
2 Zero 250
3 -100 -100
4 Zero -250
The thermal efficiency and work ratio for the cycle will be respectively.
(a) 33% and 0.66 (b) 66% and 0.36. (c) 36% and 0.66 (d) 33% and 0.36.
IES-12. A tank containing air is stirred by a paddle wheel. The work input to the
paddle wheel is 9000 kJ and the heat transferred to the surroundings from the
tank is 3000 kJ. The external work done by the system is: [IES-1999]
(a) Zero (b) 3000 kJ (c) 6000 kJ (d) 9000 kJ
IES-14. Assertion (A): The internal energy depends on the internal state of a body, as
determined by its temperature, pressure and composition. [IES-2006]
Reason (R): Internal energy of a substance does not include any energy that it
may possess as a result of its macroscopic position or movement.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IES-16. 170 kJ of heat is supplied to a system at constant volume. Then the system
rejects 180 kJ of heat at constant pressure and 40 kJ of work is done on it. The
system is finally brought to its original state by adiabatic process. If the initial
value of internal energy is 100 kJ, then which one of the following statements
is correct? [IES-2004]
(a) The highest value of internal energy occurs at the end of the constant volume process
Page 20 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
(b) The highest value of internal energy occurs at the end of constant pressure process.
(c) The highest value of internal energy occurs after adiabatic expansion
(d) Internal energy is equal at all points
IES-17. 85 kJ of heat is supplied to a closed system at constant volume. During the next
process, the system rejects 90 kJ of heat at constant pressure while 20 kJ of
work is done on it. The system is brought to the original state by an adiabatic
process. The initial internal energy is 100 kJ. Then what is the quantity of
work transfer during the process? [IES-2009]
(a) 30 kJ (b) 25 kJ (c) 20 kJ (d) 15 kJ
IES-18. A system undergoes a process during which the heat transfer to the system per
degree increase in temperature is given by the equation: [IES-2004]
dQ/dT = 2 kJ/°C The work done by the system per degree increase in
temperature is given by the equation dW/dT = 2 – 0.1 T, where T is in °C. If
during the process, the temperature of water varies from 100°C to 150°C, what
will be the change in internal energy?
(a) 125 kJ (b) –250 kJ (c) 625 kJ (d) –1250 kJ
IES-20. The internal energy of a certain system is a function of temperature alone and
is given by the formula E = 25 + 0.25t kJ. If this system executes a process for
which the work done by it per degree temperature increase is 0.75 kJ/K, then
the heat interaction per degree temperature increase, in kJ, is: [IES-1995]
(a) –1.00 (b) –0.50 (c) 0.50 (d ) 1.00
IES-21. When a gas is heated at constant pressure, the percentage of the energy
supplied, which goes as the internal energy of the gas is: [IES-1992]
(a) More for a diatomic gas than for triatomic gas
(b) Same for monatomic, diatomic and triatomic gases but less than 100%
(c) 100% for all gases
(d) Less for triatomic gas than for a diatomic gas
Page 21 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
4. The second law of thermodynamics stipulates the law of conservation of
energy and entropy.
Which of the statements are correct?
(a) 1 and 2 (b) 2 and 4 (c) 2, 3 and 4 (d) 1, 2 and 3
Enthalpy
IES-23. Assertion (A): If the enthalpy of a closed system decreases by 25 kJ while the
system receives 30 kJ of energy by heat transfer, the work done by the system
is 55 kJ. [IES-2001]
Reason (R): The first law energy balance for a closed system is (notations have
their usual meaning) ΔE = Q − W
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IES-25. A 4 kW, 20 litre water heater is switched on for 10 minutes. The heat capacity
Cp for water is 4 kJ/kg K. Assuming all the electrical energy has gone into
heating the water, what is the increase of the water temperature? [IES-2008]
(a) 15°C (b) 20°C (c) 26°C (d) 30°C
Page 22 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
IAS-2. Two ideal heat engine cycles
are represented in the given
figure. Assume VQ = QR, PQ =
QS and UP =PR =RT. If the
work interaction for the
rectangular cycle (WVUR) is
48 Nm, then the work
interaction for the other cycle
PST is:
(a) 12Nm (b) 18 Nm
IAS-2001]
(c) 24 Nm (d) 36 Nm
IAS-3. A reversible heat engine operating between hot and cold reservoirs delivers a
work output of 54 kJ while it rejects a heat of 66 kJ. The efficiency of this
engine is: [IAS-1998]
(a) 0.45 (b) 0.66 (c) 0.75 (d) 0.82
IAS-4. If a heat engine gives an output of 3 kW when the input is 10,000 J/s, then the
thermal efficiency of the engine will be: [IAS-1995]
(a) 20% (b) 30% (c) 70% (d) 76.7%
IAS-6. In a thermodynamic cycle consisting of four processes, the heat and work are
as follows: [IAS-1996]
Q: + 30, - 10, -20, + 5
W: + 3, 10, - 8, 0
The thermal efficiency of the cycle will be:
(a) Zero (b) 7.15% (c) 14.33% (d) 28.6%
IAS-7. Match List-I (Devices) with List-II (Thermodynamic equations) and select the
correct answer using the codes below the lists: [IAS-1996]
List-I List-II
A. Turbine 1. W = h2 – h1
B. Nozzle 2. h1 = h2
C. Valve 3. h1 = h2 + V2/2
D. Compressor 4. W = h1 – h2
Codes: A B C D A B C D
(a) 4 3 2 1 (b) 2 3 1 4
(c) 4 3 1 2 (d) 3 2 4 1
Page 23 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
IAS-8. Given that the path 1-2-3, a system
absorbs 100kJ as heat and does
60kJ work while along the path 1-
4-3 it does 20kJ work (see figure
given). The heat absorbed during
the cycle 1-4-3 is:
(a) - 140 Kj (b) - 80 kJ
(c) - 40kJ (d) + 60 kJ
[IAS 1994]
[IAS 1994]
IAS-13. During a process with heat and work interactions, the internal energy of a
system increases by 30 kJ. The amounts of heat and work interactions are
respectively [IAS-1999]
Page 24 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
(a) - 50 kJ and - 80 kJ (b) -50 kJ and 80 kJ
(c) 50 kJ and 80 kJ (d) 50 kJ and - 80 kJ
Enthalpy
IAS-16. The fundamental unit of enthalpy is: [IAS 1994]
(a) MLT-2 (b) ML-2T-1 (c) ML2T-2 (d) ML3T-2
IAS-18. When air is compressed, the enthalpy is increased from 100 to 200 kJ/kg. Heat
lost during this compression is 50 kJ/kg. Neglecting kinetic and potential
energies, the power required for a mass flow of 2 kg/s of air through the
compressor will be: [IAS-1997]
(a) 300 kW (b) 200 kW (c) 100 kW (d) 50 kW
Page 25 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
7. Process and temperature during phase
change
Codes: A B C D A B C D
(a) 6 5 4 3 (b) 2 1 4 3
(c) 2 5 7 4 (d) 6 1 7 4
IAS-20. A gas chamber is divided into two parts by means of a partition wall. On one
side, nitrogen gas at 2 bar pressure and 20°C is present. On the other side,
nitrogen gas at 3.5 bar pressure and 35°C is present. The chamber is rigid and
thermally insulated from the surroundings. Now, if the partition is removed,
(a) High pressure nitrogen will get throttled [IAS-1997]
(b) Mechanical work, will be done at the expense of internal energy
(c) Work will be done on low pressure nitrogen
(d) Internal energy of nitrogen will be conserved
Page 26 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
Answers with Explanation (Objective)
Page 27 of 121
Fir
rst Law
w of Therm
T odyna
amics
S K Mo
ondal’s
s Chaapter 2
⎛ v3 ⎞
⎜ × T1 − T1 ⎟
or η = 1 − γ ⎝ 1
v ⎠ = 1 − γ (v3 − v1) p1
⎛ P2 ⎞ ( p2 − p1) v1
⎜ × T1 − T1 ⎟
⎝ P1 ⎠
IES-5. Ans. (c
c) It is du = đQ
đ – đW, as u is a thermoodynamic prooperty and itts cyclic integ
gral must be
zeroo.
IES-6. Ans. (b) ΣdQ = ΣdW W or Q1− 2 + Q2 −1 = W1− 2 + W2 −1
or 20 + ( −10 ) = 50 + W2 −1 or W2 −1 = −40kJ
IES-7. Ans. (d) dQ = du + dw as u = const.
Theerefore du = 0 or dQ = d dw = 300kNm
m
IES-8. Ans. (d)
⎛ V2 ⎞
Q − Wx = Δ ⎜ h + + gz ⎟
⎝ 2 ⎠
O − Wx = −140 − 10 + 0
or Wx = 150 kJ / kg
Cha ange of internal energy = -100 kJ/kg is superfluous data.
IES-9. Ans. (b) Q = Δ E+ Δ W
Δ E = –30 kJ (ddecrease in in
nternal energ
gy)
Δ W = + 50 kJ (work
( done by the systemm)
Q = –30 + 50 = + 20 kJ
IES-10. Ans. (a
a) Net work = ∑
dW =47 74 – 180 kJ/m
min = 294 kJ
J/min = 294/6
60 kJ/s = 4.9 kW
Work done 3000 − 100
b) ηth =
IES-11. Ans. (b = = 0..66
heaat added 300
Woork ratio =
∑ ( + w) − ∑ ( −w) = 550 − 350 = 0.366
∑ ( + w) 5
550
IES-12. Ans. (a) This iss a case of constant voolume
process or an n is isochooric process.. By
perrforming worrk on the sysstem temperaature
cann be raised. In an irrev versible constant
voluume process, the systemm doesn't perrform
worrk on the surrrounding at the expense of its
inteernal energy.
IES-13. Ans. (d
d)
IES-14. Ans. (a)
( The interrnal energy depends
d only
y upon the in nal states of the system.
nitial and fin
Inteernal energyy of a substa
ance does noot include an
ny energy th hat it may possess
p as a
resuult of its ma
acroscopic position or movement.
m T
That so why in SFEE v2/2 / and gz is
there.
Page 28 of 121
Fir
rst Law
w of Therm
T odyna
amics
S K Mo
ondal’s
s Chaapter 2
If in
nternal energgy include poosition or movement then n why this v2/2
/ and gz term
ms is there.
Bur Remembe er:
Miccroscopic view of a gas is a collectioon of particlles in randoom motion. Energy E of a
parrticle consists of transla ational energy, rotatio onal energy y, vibrationnal energy
andd specific ellectronic en nergy. All thhese energies summed oveer all the parrticles of the
gass, form the sp
pecific internaal energy, e , of the gas.
b) dQ = dU + pdV
IES-15. Ans. (b if V is cons tan t ( dQ )v = ( dU)v
IES-16. Ans. (a
a)
Q2 = 180
0kJ = Δu + ΔW = Δu + ( −40))
∴U1 = 100kJ, U2 = 100 + 170 = 270
0 kJ,
U3 = 270 − 180 + 40 = 130 kJ
IES-17. Ans. (d
d) For the process
p 1-2
dQ = +85 , dW = 0
For the process
p 2-3
dQ = -90 kJ, dW = -20kJ
For the process
p 3-1
dQ = 0, dW = ?
For a cycclic process
∑ dQ = ∑ dW
⇒ 85-90+
+0 = 0-20+ dWW
⇒ -5 = -20+ dW
⇒ dW = -20+55 = +15kJ
IES-18. Ans. (c
c)
dQ = du + dw
2.dt = du + ( 2 − 0.1T
0 ) dT
0.1 150 0.1
or ∫ du = ∫ 0.1TddT =
2
× ⎡⎣T 2 ⎤⎦ =
100 2 ⎣
⎡150
02 − 1002 ⎤⎦ = 625kJ
6
Page 29 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
dW
Given: E = 25 + 0.25t kJ and = 0.75 kJ / k
dt
dE
then = 0.25 kJ / K
dt
dQ dE dW
Therefore = + = 0.25 + 0.75 kJ / K = 1.00 kJ / K
dt dt dt
IES-21. Ans. (a)
IES-22. Ans. (a) A closed system does exchange work or energy with its surroundings. option ‘3’ is
wrong. 4. “The law of conservation of entropy” is imaginary so option ‘4’ is also wrong.
IES-23. Ans. (a)
v2 dQ v2 dw
IES-24. Ans. (b) h1 + 1 + gz1 + = h2 + 2 + gz2 + =0
2 dm 2 dm
dw
For boiler v1, v2 is negligible and z1 = z2 and =0
dm
dQ
or = ( h2 − h1 )
dm
IES-25. Ans. (d)
mCP ΔT = ( 4 × 10 × 60 )
⇒ 20 × 4 × ΔT = 2400
⇒ ΔT = 30C°
IES-26. Ans. (c) Enthalpy of additional gas will be converted to internal energy.
Uf= miui+(mf-mi)hp = 0.25x200+(1-0.25)x400 = 350 kJ
As total mass = 1kg, uf=350 kJ/kg
Note: You cannot simply use adiabatic mixing law here because it is not closed system.
This is a problem of variable flow process. If you calculate in following way it will be
wrong.
Final internal energy of gas(mixture) is
m u + m 2 u2
u= 1 1
m1 + m2
⎛ kJ ⎞ ⎛ kJ ⎞
(0.25kg) ⎜ 200 ⎟ + (0.75kg) ⎜ 300
⎝ kg ⎠ ⎝ kg ⎟⎠
u=
(0.25 + 0.75)kG
kJ
u = 275
kg
It is valid for closed system only.
Page 30 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
1 1
Areas Δ PTS= Area (WVUR) ∴ Work PTS= × 48 =24 Nm
2 2
work output work out put 54
IAS-3. Ans. (a) η = = = = 0.45
Heat input work output + heat rejection 54 + 66
W 3 × 103 watts
IAS-4. Ans. (b) Thermal efficiency = = = 0.3 = 30%
Q 10.000 J/s
IAS-5. Ans. (c)
Q1− 2 = (U2 − U1 ) + W1−2
or 0 = (U2 − U1 ) + ( −5000 ) or (U2 − U1 ) = 5000 J
Q2−1 = (U1 − U2 ) + W2−1
or W2−1 = Q2−1 − (U1 − U2 ) = Q2−1 + (U2 − U1 ) = 1000 + 5000 = 6000 J
IAS-6. Ans. (c) Net work output = 3 + 10 – 8 = 5 unit and Heat added = 30 + 5 = 35 unit
5
Therefore efficiency, η = × 100% = 14.33%
35
IAS-7. Ans. (a)
IAS-8. Ans. (d) Q123 = U13 + W123 or, 100 = U13 + 60 or, U13 = 40 kJ
And Q143 = U13 + W143 = 40+20 = 60 kJ
1
IAS-9.Ans. (b) Total work = 5 × 3 + × 5 × 1 = 17.5 J or δW = du + δW = 2.5 + 17.5 = 20 J
2
Area under 500 and 1500
IAS-10. Ans. (c) Efficiency =
Area under 0 and 1500
1
× {(5 − 1) + (4 − 2)} × (1500 − 500)
2 3000
= = = 0.6
1 5000
× {(5 − 1) + (4 − 2)} × (1500 − 500) + (5 − 1) × 500
2
IAS-11. Ans. (a)
IAS-12. Ans. (b) Internal energy is a property of a system so ∫ du = 0
IAS-13. Ans. (a) dQ = du + dW if du = +30kJ then dQ = −50kJ and dW = −80kJ
IAS-14. Ans. (b) δW = du + δW = du + pdV
or 84 × 103J = du + 1 × 106 × (0.06 – 0.03) = du +30 kJ or du = 83 – 30 = 54 kJ
IAS-15. Ans. (a) Q1-2 = U2 –U1 +W1-2
Or 0 = U2 –U1 - 6000
or U2 –U1 = +6000
Q2-1 = U1-U2+W2-1
or W2-1 = Q2-1 - (U1-U2)
=1000+6000=7000J
Page 31 of 121
First Law of Thermodynamics
S K Mondal’s Chapter 2
IAS-17. Ans. (a) Energy balance gives as
dW dQ
= ( Δh )air + ( Δh ) water +
dm dm
dQ
or = 90 − 30 − 40
dm
= 20kJ / kg of air compressed.
Page 32 of 121
Second Law of Thermodynamics
S K Mondal’s Chapter 3
IES-2. Assertion (A): Second law of thermodynamics is called the law of degradation
of energy. [IES-1999]
Reason (R): Energy does not degrade each time it flows through a finite
temperature difference.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
Page 33 of 121
Second Law of Thermodynamics
S K Mondal’s Chapter 3
Clausius' Statement of the Second Law
IES-5. Assertion (A): Heat cannot spontaneously pass from a colder system to a hotter
system without simultaneously producing other effects in the surroundings.
Reason (R): External work must be put into heat pump so that heat can be
transferred from a cold to a hot body. [IES-1999]
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
Clausius' Theorem
IES-6. A steam power plant is shown in
figure,
(a) The cycle violates first and
second laws of thermodynamics.
(b) The cycle does not satisfy the
condition of Clausius inequality.
(c) The cycle only violates the second
laws of thermodynamics
(d) The cycle satisfies the Clausius
inequality
[IES-1992]
IES-7. An inventor says that his new concept of an engine, while working between
temperature limits of 27°C and 327°C rejects 45% of heat absorbed from the
source. His engine is then equivalent to which one of the following engines?
(a) Carnot engine (b) Diesel engine [IES-2009]
(c) An impossible engine (d) Ericsson engine
Page 34 of 121
Second Law of Thermodynamics
S K Mondal’s Chapter 3
temperature T2 and rejected to a reservoir at temperature T3. If the efficiencies
of the engines are same then the relationship between T1, T2 and T3 is given by:
[IES-2002]
(T1 + T3 ) (T1 + 2T3 )
(a) T2 =
2
(b) T2 = (T
1
2
+ T32 ) (c) T2 = T1T3 (d) T2 =
2
IES-10. A reversible engine operates between temperatures 900 K & T2 (T2 < 900 K), &
another reversible engine between T2 & 400 K (T2 > 400 K) in series. What is the
value of T2 if work outputs of both the engines are equal? [IES-2005]
(a) 600 K (b) 625 K (c) 650 K (d) 675 K
IES-11. Two reversible engine operate between thermal reservoirs at 1200 K, T2K and
300 K such that 1st engine receives heat from 1200 K reservoir and rejects heat
to thermal reservoir at T2K, while the 2nd engine receives heat from thermal
reservoir at T2K and rejects heat to the thermal reservoir at 300 K. The
efficiency of both the engines is equal. [IES-2004]
What is the value of temperature T2?
(a) 400 K (b) 500 K (c) 600 K (d) 700 K
IES-13. An engine working on Carnot cycle rejects 40% of absorbed heat from the
source, while the sink temperature is maintained at 27°C, then what is the
source temperature? [IES-2009]
(a) 750°C (b) 477°C (c) 203°C (d) 67.5°C
IES-14. A reversible heat engine rejects 50 percent of the heat supplied during a cycle
of operation. If this engine is reversed and operates as a heat pump, then what
is its coefficient of performance? [IES-2009]
(a) 1.0 (b) 1.5 (c) 2.0 (d) 2.5
IES-15. A heat engine is supplied with 250 kJ/s of heat at a constant fixed temperature of
227°C; the heat is rejected at 27°C, the cycle is reversible, then what amount of
heat is rejected? [IES-2009]
(a) 250 kJ/s (b) 200 kJ/s (c) 180 kJ/s (d) 150 kJ/s
IES-16. One reversible heat engine operates between 1600 K and T2 K, and another
reversible heat engine operates between T2K and 400 K. If both the engines
have the same heat input and output, then the temperature T2 must be equal
to: [IES-1993]
(a) 1000 (b) 1200 (c) 1400 (d) 800
Page 35 of 121
Second Law of Thermodynamics
S K Mondal’s Chapter 3
Previous 20-Years IAS Questions
Kelvin-Planck Statement of Second Law
IAS-1. Assertion (A): No machine would continuously supply work without
expenditure of some other form of energy. [IAS-2001]
Reason (R): Energy can be neither created nor destroyed, but it can only be
transformed from one form into another.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IAS-5. In a cyclic heat engine operating between a source temperature of 600°C and a
sink temperature of 20°C, the least rate of heat rejection per kW net output of
the engine is: [IAS 1994]
(a) 0.460 kW (b) 0.505 kW (c) 0.588 kW (d) 0.650 kW
Page 36 of 121
Second Law of Thermodynamics
S K Mondal’s Chapter 3
Answers with Explanation (Objective)
Page 37 of 121
Seco
ond La
aw of Therm
modyn
namicss
S K Mo
ondal’s
s Cha
apter 3
IES-12. Ans. (c
c)
Sou ature = T1,
urce Tempera
ermediate Temperature = T
Inte
Sin
nk Temperatuure = T2
∵ W1 = W2
⎛ T⎞ ⎛ T ⎞
Q1 ⎜ 1 − ⎟ = Q2 ⎜ 1 − 2 ⎟
⎝ T1 ⎠ ⎝ T⎠
T1 ⎛ T ⎞ ⎛ T2 ⎞ T1 T2
⇒ ⎜1− ⎟ = 1− ⎟ ⇒ − 1 = 1−
T ⎝ T1 ⎠ ⎜⎝ T⎠ T T
T1 + T2 T + T2 180 + 20
0
⇒ =2 ⇒T = 1 = = 100°C
T 2 2
IES-13. Ans. (b
b) Sink temp perature = 277°C = 27 + 2773 = 300K
It is given that engine rejeccts 40% of ab bsorbed heat from the
souurce
Q Q
Forr a carnot cyccle engine 1 = 2
T1 T2
Q 0.44Q 30
00
= ⇒T= = 750K = 477°C
T 30
00 0..4
Q1 Q2
IES-14. Ans. (c
c) =
T1 T2
Q 0.5 Q1 T2
⇒ 1 = ⇒ = 0.5
T1 T2 T1
If the engine is reversed an nd operated as
a the Heat
Pummp.
Theen COP coeffficient of perfformance
T1 1 1
= = = =2
T1 − T2 T2 1 − 0.5
5
1−
T1
IES-15. Ans. (d
d) Heat supp
plied by the Heat
H Engine = Q1 = 250 kJ/sec
k
Souurce temperaature = 227°C = 500 K
Sinnk temperatuure = 27°C = 300K
3
2500 Q
= 2 ⇒ Q 2 = 250 × 0.6 = 150kJ / sec
5000 300
IES-16. Ans. (d
d) Two reverrsible heat en
ngines operatte between liimits of
16000K and T2; T2 and 40
00K
Botth have the same heat inp put and output,
T1 − T2 1600 − T2 T2 − 4000
i.e.. is same for booth or = or T2 = 8000 K
T1 16000 T2
Page 38 of 121
Second Law of Thermodynamics
S K Mondal’s Chapter 3
Previous 20-Years IAS Answers
IAS-1. Ans. (a)
Q1 Q2
IAS-2. Ans. (d) =
T1 T2
IAS-3. Ans. (b) ∑Q = ∑W
300 + Q1 + Q2 = 50
IAS-4. Ans. (b) For reversible cycle
T1 T2 T3
= =
Q1 Q2 T3
T1 − T2 Q1 − Q2
or =
T2 Q2
T2
or T1 − T2 = (Q1 − Q2 ) ×
Q2
T3
Similarly T2 − T3 = ( Q2 − Q3 ) ×
Q3
If T1 − T2 = T2 − T3 then Q1 − Q2 = Q2 − Q3
or W1 = W2
Q1 Q2 Q1 − Q2 W
IAS-5. Ans. (b) Reversible engine has maximum efficiency where = = =
T1 T2 T1 − T2 T1 − T2
Page 39 of 121
Entropy
S K Mondal’s Chapter 4
4. Entropy
GATE-3. The entropy change for the Universe during the process in kJ/K is: [GATE-2003]
(a) 0.4652 (b) 0.0067 (c) 0 (d) –0.6711
Page 40 of 121
Entropy
S K Mondal’s Chapter 4
(c) Equal to zero
(d) Always positive
IES-4. A Carnot engine operates between 327°C and 27°C. If the engine produces 300
kJ of work, what is the entropy change during heat addition? [IES-2008]
(a) 0.5 kJ/K (b) 1.0 kJ/K (c) 1.5 kJ/K (d) 2.0 kJ/K
Page 41 of 121
Entropy
S K Mondal’s Chapter 4
Temperature-Entropy Plot
IES-5. A system comprising of a pure
substance executes reversibly a
cycle 1 -2 -3 -4 -1 consisting of two
isentropic and two isochoric
processes as shown in the Fig. 1.
[IES-2002]
Page 42 of 121
Enttropy
S K Mo
ondal’s
s Cha
apter 4
[IES-1995]
[IES-1997]
Thee same cyc
cle, when re
epresented on the pre
essure-volum
me coordin
nates takes
the
e form
Page 43 of 121
Enttropy
S K Mo
ondal’s
s Cha
apter 4
Cod
des: A B C A B C
(a) 1 2 3 (b) 2 3 1
(c) 3 1 2 (d) 3 2 1
IES-9. A cyclic
c proce
ess ABCD shown
s in
the
e V-T diagra
am perform
med with
a constant
c ma
ass of an id
deal gas.
The
e process of
o p-V diagr
ram will
be as shown in
n
[IES-1992]
Page 44 of 121
Entropy
S K Mondal’s Chapter 4
Codes: A B C A B C
(a) 1 2 3 (b) 2 3 1
(c) 3 2 1 (d) 1 3 2
IES-11. Two polytropic processes undergone by a perfect gas are shown below in the
pressure-volume co-ordinates. [IES-2008]
Page 45 of 121
Entropy
S K Mondal’s Chapter 4
IES-14. For a thermodynamic cycle to be irreversible, it is necessary that [IES-1998]
δQ δQ δQ δQ
(a) ∫ =0 (b) ∫ <0 (c) ∫ >0 (d) ∫ ≥0
T T T T
IES-19. A system of 100 kg mass undergoes a process in which its specific entropy
increases from 0.3 kJ/kg-K to 0.4 kJ/kg-K. At the same time, the entropy of the
surroundings decreases from 80 kJ/K to 75 kJ/K. The process is: [IES-1997]
(a) Reversible and isothermal (b) Irreversible
(c) Reversible (d) Impossible
IES-20. Which one of the following temperature entropy diagrams of steam shows the
reversible and irreversible processes correctly? [IES-1996]
Page 46 of 121
Entropy
S K Mondal’s Chapter 4
IES-22. The entropy of a mixture of ideal gases is the sum of the entropies of
constituents evaluated at: [IES-2005]
(a) Temperature and pressure of the mixture
(b) Temperature of the mixture and the partial pressure of the constituents
(c) Temperature and volume of the mixture
(d) Pressure and volume of the mixture
IES-23. The heat added to a closed system during a reversible process is given by
Q = α T + β T 2 , where α and β are constants. The entropy change of the system
as its temperature changes from T1 to T2 is equal to: [IES-2000]
⎡ β 2 ⎤
(a ) α + β (T2 − T1 ) (b) ⎢α (T2 − T1 ) +
⎣ 2
( )
T2 − T12 ⎥ / T1
⎦
⎡α β 3 ⎤ ⎛ T2 ⎞
(
(c) ⎢ T22 − T12 +
⎣2
) ( )
T2 − T13 ⎥ / T12
⎦
( d ) α ln ⎜ ⎟ + 2β (T2 − T1 )
2 ⎝ T1 ⎠
Page 47 of 121
Entropy
S K Mondal’s Chapter 4
temperature 100 K, then the thermal efficiency of the engine is approximately
equal to: [IES-2002]
(a) 65% (b) 75% (c) 80% (d) 85%
IES-26. A reversible engine exceeding 630 cycles per minute drawn heat from two
constant temperature reservoirs at 1200 K and 800 K rejects heat to constant
temperature at 400 K. The engine develops work 100kW and rejects 3200 KJ
Q1200
heat per minute. The ratio of heat drawn from two reservoirs is nearly.
Q800
[IES-1992]
(a) 1 (b) 1.5 (c) 3 (d) 10.5
IES-27. In which one of the following situations the entropy change will be negative
(a) Air expands isothermally from 6 bars to 3 bars [IES-2000]
(b) Air is compressed to half the volume at constant pressure
(c) Heat is supplied to air at constant volume till the pressure becomes three folds
(d) Air expands isentropically from 6 bars to 3 bars
Page 48 of 121
Enttropy
S K Mo
ondal’s
s Cha
apter 4
Te
empera
ature-Entropy Plot
IA
AS-3. An ideal cyclle is shownn in the
giv
ven pressure
e-volume diiagram:
[IAS-1997]
The
e same cyclle on temperature-entr
ropy diagram will be re
epresented as:
AS-4.
IA The e thermaal efficien
ncy of t
the
hyp pothetical heat
h engine
e cycle show
wn
in the
t given figure is:
(a) 0.5 (b) 0.45
(c) 0.35
0 (d) 0.25
[IAS-2000]
AS-5.
IA Wh hich one of the followiing pairs be
est expresses a relatio onship similar to that
exppressed in the pair r “pressure e-volume” for a the ermodynam mic system
und dergoing a process? [IAS-1995]
(a) Enthalpy-enntropy (b) Pressu
ure-enthalpy
(c) Pressure-tem
P mperature (d) Tempeerature-entroopy
IA
AS-6. An ideal gas contained
c in
n a rigid ta
ank
is cooled
c suchh that T2 < and P2 <P1 In
thee given temperatu ure entro
opy
diaagram, th
his processs path is
reppresented by the line la
abelled.
(a) A (b) B
(c) C (d) D
[IAS-1999]
Page 49 of 121
Enttropy
S K Mo
ondal’s
s Cha
apter 4
AS-7.
IA In the T-S diiagram shown in the
ure, which one of the
figu e following
is represented
r d by the area
a under
thee curve?
(a) Total work done
d during the process
(b) Total heat absorbed during the
process
(c) Total heatt rejected during
d the
process
(d) Degree of irreversibility
[IAS-2004]
The Ineq
quality of Clau
usius
IA
AS-8. Cla
ausius inequ
uality is sta
ated as [IAS-2001]
Q Q
(a) ∫ δQ < 0 (b) ∫ δQ = 0 (c)) ∫ δ >0 (d) ∫δ T ≤0
T
IA
AS-9. For
r real therm
modynamic cycle: [IAS-2003]
dQ dQ dQ dQ
(a) ∫ T
> 0 butt < ∞ (b) ∫ T
<0 (c)) ∫ T
=0 (d) ∫ T
=∞
IA
AS-10(i). If a system undergoes an
a irreversiible adiabatic processs, then (sym
mbols have
usuual meaning
gs) [IAS-1999]
dQ dQ
(a) ∫T
= 0 an
nd ΔS > 0 (b) ∫T
= 0 and ΔS = 0
dQ dQ
(c) ∫ > 0 an
nd ΔS = 0 (d) ∫ < 0 and ΔS < 0
T T
IA
AS-10(ii). A cyclic
c heat engine rece
eives 600 kJ of heat fr
rom a 1000 K source and
a rejects
dQ
450
0 kJ to a 300
3 K sink. The quanttity ∫ T
a
and efficien
ncy of the engine
e are
resspectively [IAS-2001]
(a) 2.1 kJ/K andd 70% (b)) –0.9 kJ/K and
a 25%
(c) + 0.9 kJ/K an
nd 70% (d)) –2.1 kJ/K and
a 25%
A
Applicattions off Entrop
py Prin
nciple
IA
AS-11. Wh hich one of the
t followinng statemen nts is not co orrect? [IAS-2003]
(a) Change in entropy
e durin
ng a reversiblle adiabatic process
p is zerro
(b) Entropy increases with the
t addition of heat
(c) Throttling is a constant entropy expa ansion processs
(d) Change in entropy wh hen a gas is heated under u consta ant pressure given by
T2
s2 − s1 = mC
C p log e
T1
Page 50 of 121
Entropy
S K Mondal’s Chapter 4
IAS-12. Assertion (A): Entropy change for a reversible adiabatic process is zero.
Reason (R): There is no heat transfer in an adiabatic process. [IAS 1994]
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IAS-14. An electric motor of 5 kW is subjected to a braking test for 1 hour. The heat
generated by the frictional forces in the process is transferred to the
surroundings at 20°C. The resulting entropy change will be: [IAS-1998]
(a) 22.1 kJ/K (b) 30.2 kJ/K (c) 61.4 kJ/K (d) 82.1 kJ/K
IAS-16. In which one of the following processes is there an increase in entropy with no
degradation of energy? [IAS-1996]
(a) Polytropic expansion (b) Isothermal expansion
(c) Isochoric heat addition (d) Isobaric heat addition
Page 51 of 121
Enttropy
S K Mo
ondal’s
s Cha
apter 4
Answ
wers with Expla
anatio
on (Ob
bjectiv
ve)
Previo
ous 20-Years
s GATE
E Answ
wers
GA
ATE-1. Ans. –11858 J/K, 12787 J/K.
⎛υ ⎞ ⎛υ ⎞ ⎛2⎞
ATE-2. Ans. (b) w1− 2 = mRT
GA m In ⎜ 2 ⎟ = pυ In ⎜ 2 ⎟ = 200 × 1× In ⎜ ⎟ kJ = 138.6 kJ
k
⎝ υ1 ⎠ ⎝ υ1 ⎠ ⎝ 1⎠
GA ersible processs so ( ΔS )univerrse = 0
ATE-3. Ans. (c) It is reve
GA
ATE-4. Ans. (d)
GA
ATE-5. Ans.. (d) It is a case of spoontaneous prrocess i.e. irrrepressibility
y involved that
t so why
entropy change of the univerrse is positiv
ve.
Page 52 of 121
Enttropy
S K Mo
ondal’s
s Cha
apter 4
IES-12. Ans. (b
b)
IES-13. Ans. (b
b)
IES-14. Ans. (b
b)
IES-15. Ans. (c
c)
dQ
IES-16. Ans. (a
a) ∫ T
= 0 does not neccessarily meaans reversiblle process. If dQ = 0 .
IES-17. Ans. (c) In irreversible
i heat
rejeection process enttropy
deccreases. In an irreverrsible
process entropy
y of the univverse
ways increasses i.e. sum
alw m of
systtem + su urroundings will
incrreases.
Con nsider the prrocess 3–4 iff it is
irreeversible prrocess then also
entropy will deccrease.
IES-18. Ans. (c)
( In reversiible adiabaticc expansion, entropy chan nge is zero and no changee in entropy
of surroundings
s s.
IES-19. Ans. (b
b) Entropy inncrease in prrocess = 100 (0.4 – 0.3) = 10 kJ/kg
Enttropy change e of surround
dings = 5 kJ/K K
Thu us net entrop
py increases and
a the proceess is irreverrsible.
IES-20. Ans. (c)
( In reversiible process entropy
e channge is zero an
nd in four figuures it is rep
presented by
straaight vertical line. Howevver, in irreveersible processs, entropy in
ncreases in all
a processes
(exppansion as well
w as compression).
IES-21. Ans. (b
b)
( T1 − T2 ) ΔS = W
300
or ΔS = = 1 kJ / k
600 − 300
IES-22. Ans. (c
c)
dQ 1 α + 2 β T ⎛ T2 ⎞
T1 T
IES-23. Ans. (d
d) ∫T T T∫ T
= T
dT = α ln ⎜ ⎟ + 2 β (T2 − T1 )
⎝ T1 ⎠
1 1
Page 53 of 121
Entropy
S K Mondal’s Chapter 4
IES-24. Ans. (c)
Qs1 Qs2 QR
Thus, + − =0
1200 800 400
Qs1 9.2 × 106 − Q 6 × 3.2 × 106
or + − =0
1200 800 400
2Qs1 + 3(9.2 × 106 − Qs1 ) − 6 × 3.2 × 106
=0
2400
or Qs1 = 3 × 9.3 × 106 − 6 × 3.2 × 106
= 8.4 × 106 J/min
Qs2 = 9.2 × 106 − 8.4 × 106
= 0.8 × 106 J/min
Page 54 of 121
Enttropy
S K Mo
ondal’s
s Cha
apter 4
8.4
He
ence ratio = =10.5
0.8
b) It is isoba
IES-27. Ans. (b aric compresssion.
IES-28. Ans. (d
d)
Previious 20
0-Yearrs IAS Answ
wers
IA
AS-1. Ans. (b)
IA
AS-2. Ans. (b)
+Q
S2 = = 10
0
500
or Q = 5000 kJJ
−Q −5000
S1 = = = −5kJ / k
1000 1000
1
⎡∴Heat added tot thesystemm is +ive ⎤
⎢ Heat rejecteed from the syystem is -ive ⎥
⎣ ⎦
IA
AS-3. Ans. (d)
1
× ( 5 − 1) × ( 800 − 40
00 )
Work done
d area1 − 2 − 3 2
AS-4. Ans. (d) η =
IA = = = 0.25
dded areaunder curve 2 − 3
Heat ad ( 5 − 1) × 800
IA
AS-5. Ans. (d) That so wh
hy we are usin
ng p–v or T–
–s diagram.
IA
AS-6. Ans. (a))
IA
AS-7. Ans. (b
b)
IA
AS-8. Ans. (d)
IA
AS-9. Ans. (b)
Page 55 of 121
Entropy
S K Mondal’s Chapter 4
dQ
IAS-10(i). Ans. (a) ∫
T
= 0 does not necessarily means reversible process. If dQ = 0 .
Q − Q2 Q 450
IAS-10(ii). Ans. (b) η = 1 = 1− 2 = 1− = 0.25 = 25%
Q1 Q1 600
IAS-11. Ans. (c) Throttling is a constant enthalpy expansion process.
IAS-12. Ans. (b)
dQ dQ 1600 1600
IAS-13. Ans. (c) Entropy generated = dsat 400K − dsat 800K = − = − = 2kJ / K
400 800 400 800
ΔQ 5 × 3600
IAS-14. Ans. (c) ΔS = = kJ / K = 61.4kJ / K
T 293
IAS-15. Ans. (a)
IAS-16. Ans. (b)
Page 56 of 121
Availability, Irreversibility
S K Mondal’s Chapter 5
5. Availability, Irreversibility
Availability
GATE-2. Availability of a system at any given state is: [GATE-2000]
(a) A property of the system
(b) The maximum work obtainable as the system goes to dead state
(c) The total energy of the system
(d) The maximum useful work obtainable as the system goes to dead state
GATE-3. A heat reservoir at 900 K is brought into contact with the ambient at 300 K for
a short time. During this period 9000 kJ of heat is lost by the heat reservoir.
The total loss in availability due to this process is: [GATE-1995]
(a) 18000 kJ (b) 9000 kJ (c) 6000 kJ (d) None of the above
Irreversibility
GATE-4. Consider the following two processes: [GATE-2010]
a. A heat source at 1200 K loses 2500 kJ of heat to sink at 800 K
b. A heat source at 800 K loses 2000 kJ of heat to sink at 500 K
Which of the following statements is TRUE?
(a) Process I is more irreversible than Process II
(b) Process II is more irreversible than Process I
(c) Irreversibility associated in both the processes is equal
(d) Both the processes are reversible
Page 57 of 121
Availability, Irreversibility
S K Mondal’s Chapter 5
Previous 20-Years IES Questions
Available Energy
IES-1. What will be the loss of available energy associated with the transfer of 1000 kJ
of heat from constant temperature system at 600 K to another at 400 K when
the environment temperature is 300 K? [IES-2004]
(a) 150 kJ (b) 250 kJ (c) 500 kJ (d) 700 kJ
IES-2. What is the loss of available energy associated with the transfer of 1000 kJ of
heat from a constant temperature system at 600 K to another at 400 K when the
environmental temperature is 300 K? [IES-2008]
(a) 150 kJ (b) 250 kJ (c) 166·67 kJ (d) 180kJ
Availability
IES-4. Assertion (A): The change in availability of a system is equal to the change in
the Gibbs function of the system at constant temperature and pressure.
Reason (R): The Gibbs function is useful when evaluating the availability of
systems in which chemical reactions occur. [IES-2006]
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IES-5. For a steady flow process from state 1 to 2, enthalpy changes from h1 = 400
kJ/kg to h2 = 100 kJ/kg and entropy changes from s1 = 1.1 kJ/kg-K to s2 = 0.7
kJ/kg-K. Surrounding environmental temperature is 300 K. Neglect changes in
kinetic and potential energy. The change in availability of the system is:
[IES-2003]
(a) 420 kJ/kg (b) 300 kJ/kg (c) 180 kJ/kg (d) 90 kJ/kg
Page 58 of 121
Availability, Irreversibility
S K Mondal’s Chapter 5
2. Clapeyron's equation for dry saturated steam is given by
dTs ⎡ hg − hf ⎤
(V g − Vf ) = ⎢
dQ ⎣ Ts ⎦
⎥
3. A gas can have any temperature at a given pressure unlike a vapour which
has a fixed temperature at a given pressure.
⎡ ∂s ⎤
4. Joule Thomson coefficient is expressed as μ = ⎢ ⎥
⎣ ∂p ⎦ h
Of these statements
(a) 1, 2 and 3 are correct (b) 1, 3 and 4 are correct
(c) 2 and 3 are correct (d) 1, 2 and 4 are correct
IES-8. 10kg of water is heated from 300 K to 350 K in an insulated tank due to
churning action by a stirrer. The ambient temperature is 300 K. In this context,
match List-I and List-II and select the correct answer using the codes given
below the Lists: [IES-2000]
List-I List-II
A. Enthalpy change 1. 12.2 kJ/kg
B. Entropy change/kg 2. 1968 kJ
C. Availability/kg 3. 2090 kJ
D. Loss of availability 4. 656 J/kg-k
Codes: A B C D A B C D
(a) 3 1 4 2 (b) 2 4 1 3
(c) 3 4 1 2 (d) 2 1 4 3
IES-9. Neglecting changes in kinetic energy and potential energy, for unit mass the
availability in a non-flow process becomes a = ɸ - ɸo, where ɸ is the availability
function of the [IES-1998]
(a) Open system (b) Closed system
(c) Isolated system (d) Steady flow process
Irreversibility
IES-11. The irreversibility is defined as the difference of the maximum useful work
and actual work: I = Wmax,useful- Wactual. How can this be alternatively expressed?
(a) I = To ( ΔS system + ΔS surrounding ) (b) I = To ( ΔS system − ΔS surrounding ) [IES-2005]
IES-12. Assertion (A): All constant entropy processes are adiabatic, but all adiabatic
processes are not isentropic. [IES-2006]
Page 59 of 121
Availability, Irreversibility
S K Mondal’s Chapter 5
Reason (R): An adiabatic process which resists the exchange of energy to the
surroundings may have irreversibility due to friction and heat conduction.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
Available Energy
IAS-1. What will be the loss of available energy associated with the transfer of 1000 kJ
of heat from constant temperature system at 600 K to another at 400 K when
the environment temperature is 300 K? [IAS-1995]
(a) 150 kJ (b) 250 kJ (c) 500 kJ (d) 700 kJ
IAS-2. An inventor claims that heat engine has the following specifications: [IAS-2002]
Power developed = 50 kW; Fuel burned per hour = 3 kg
Heating value of fuel =75,000 kJ per kg; Temperature limits = 627°C and 27°C
Cost of fuel = Rs. 30/kg; Value of power = Rs. 5/kWh
(a) Possible (b) Not possible (c) Economical (d) Uneconomical
IAS-3. For a reversible power cycle, the operating temperature limits are 800 K and
300 K. It takes 400 kJ of heat. The unavailable work will be: [IAS-1997]
(a) 250 kJ (b) 150 kJ (c) 120 kJ (d) 100 kJ
Quality of Energy
IAS-4. Increase in entropy of a system represents [IAS-1994]
(a) Increase in availability of energy (b) Increase in temperature
(c) Decrease in pressure (d) Degradation of energy
Availability
IAS-5. If u, T, v, s, hand p refer to internal energy, temperature, volume, entropy,
enthalpy and pressure respectively; and subscript 0 refers to environmental
conditions, availability function for a closed system is given by: [IAS-2003]
(a) u + Po v – To s (b) u – Po v+ To s (c) h + Po v – Tos (d) h – Po v + To s
IAS-6. Match List-I with List-II and select the correct answer using the codes given
below the lists:
List-I List-II
Page 60 of 121
Availability, Irreversibility
S K Mondal’s Chapter 5
A. Irreversibility 1. Mechanical equivalent
B. Joule Thomson experiment 2. Thermodynamic temperature scale
C. Joule's experiment 3. Throttling process
D. Reversible engines 4. Loss of availability
Codes: A B C D A B C D
(a) 1 2 3 4 (b) 1 2 4 3
(c) 4 3 2 1 (d) 4 3 1 2
Irreversibility
IAS-7. The loss due to irreversibility
in the expansion valve of a
refrigeration cycle shown in
the given figure is
represented by the area
under the line.
(a) GB (b) AG
(c) AH (d) BH
[IAS-1999]
IAS-8. Assertion (A): When a gas is forced steadily through an insulated pipe
containing a porous plug, the enthalpy of gas is the same on both sides of the
plug. [IAS-1997]
Reason (R): The gas undergoes an isentropic expansion through the porous
plug.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
Page 61 of 121
Availability, Irreversibility
S K Mondal’s Chapter 5
Answers with Explanation (Objective)
Page 62 of 121
Availability, Irreversibility
S K Mondal’s Chapter 5
Page 63 of 121
Availability, Irreversibility
S K Mondal’s Chapter 5
IAS-7. Ans. (d) Entropy will increase in the process AH is BH.
Therefore Irreversibility (I) = To × ΔS i.e. area under the line BH.
IAS-8. Ans. (c) Expansion through the porous plug is adiabatic as no heat added or rejected to the
system. It is not reversible, due to large irreversibility entropy increases so it is not an
isentropic process.
mimimum energy int ake to perform the given task
IAS-9. Ans. (c) ηII =
actual energy int ake to perform the same task
Page 64 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
6. Thermodynamic Relations
Maxwell's Equations
GATE-1. Which of the following relationships is valid only for reversible processes
undergone by a closed system of simple compressible substance (neglect
changes in kinetic and potential energy? [GATE-2007]
(a) δQ = dU + δW (b) TdS = dU + pdV (c) TdS = dU + δW (d) δQ = dU + pdV
GATE-2. Considering the relationship TdS = dU + pdV between the entropy (S), internal
energy (U), pressure (p), temperature (T) and volume (V), which of the
following statements is correct? [GATE-2003]
(a) It is applicable only for a reversible process
(b) For an irreversible process, TdS > dU + pdV
(c) It is valid only for an ideal gas
(d) It is equivalent to 1 law, for a reversible process
GATE-6. A 2 kW, 40 litre water heater is switched on for 20 minutes. The heat capacity
Cp for water is 4.2 kJ/kg K. Assuming all the electrical energy has gone into
heating the water, increase of the water temperature in degree centigrade is:
[GATE-2003]
Page 65 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
(a) 2.7 (b) 4.0 (c) 14.3 (d) 25.25
GATE-9. A gas having a negative Joule-Thompson coefficient (µ < 0), when throttled,
will: [GATE-2001]
(a) Become cooler
(b) Become warmer
(c) Remain at the same temperature
(d) Either be cooler or warmer depending on the type of gas
GATE-10. Match 4 correct pairs between List-I and List-II for the questions [GATE-1994]
For a perfect gas:
List-I List-II
(a) Isobaric thermal expansion coefficient 1. 0
(b) Isothermal compressibility 2. ∞
(c) Isentropic compressibility 3. 1/v
(d) Joule – Thomson coefficient 4. 1/T
5. 1/p
6. 1/ γ p
Page 66 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
Maxwell's Equations
IES-2. Which thermodynamic property is evaluated with the help of Maxwell
equations from the data of other measurable properties of a system? [IES 2007]
(a) Enthalpy (b) Entropy (c) Latent heat (d) Specific heat
TdS Equations
IES-4. T ds equation can be expressed as: [IES-2002]
T β dv Tdv
(a) Tds = Cv dT + (b) Tds = Cv dT +
k k
Tk Tβ
(c) Tds = Cv dT + dv (d) Tds = Cv dT + dp
β k
IES-5. Which one of the following statements applicable to a perfect gas will also be
true for an irreversible process? (Symbols have the usual meanings). [IES-1996]
(a) dQ = du + pdV (b) dQ = Tds (c) Tds = du + pdV (d) None of the above
Page 67 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
D. Difference between specific heats at constant 1 ⎛ ∂v ⎞
pressure and at constant Cp – Cv 4. − ⎜ ⎟
v ⎝ ∂p ⎠T
Codes: A B C D A B C D
(a) 3 4 2 1 (b) 4 1 3 2
(c) 3 4 1 2 (d) 4 1 2 3
IES-8. Assertion (A): Specific heat at constant pressure for an ideal gas is always
greater than the specific heat at constant volume. [IES-2002]
Reason (R): Heat added at constant volume is not utilized for doing any
external work.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IES-9. An insulated box containing 0.5 kg of a gas having Cv = 0.98 kJ/kgK falls from a
balloon 4 km above the earth’s surface. What will be the temperature rise of the
gas when the box hits the ground? [IES-2004]
(a) 0 K (b) 20 K (c) 40 K (d) 60 K
IES-10. As compared to air standard cycle, in actual working, the effect of variations in
specific heats is to: [IES-1994]
(a) Increase maximum pressure and maximum temperature
(b) Reduce maximum pressure and maximum temperature
(c) Increase maximum pressure and decrease maximum temperature
(d) Decrease maximum pressure and increase maximum temperature
Page 68 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
(c) A is true but R is false
(d) A is false but R is true
IES-15. It can be shown that for a simple compressible substance, the relationship
⎛ ∂V ⎞ ⎛ ∂P ⎞
2
Cp – Cv = – T ⎜ ⎟ ⎜ ⎟ exists. [IES-1998]
⎝ ∂T ⎠ p ⎝ ∂v ⎠T
Where C p and C v are specific heats at constant pressure and constant volume
respectively. T is the temperature V is volume and P is pressure.
Which one of the following statements is NOT true?
(a) C p is always greater than C v.
(b) The right side of the equation reduces to R for ideal gas.
⎛ ∂P ⎞ ⎛ ∂V ⎞
2
IES-19. Assertion (A): Throttling process for real gases at initial temperature higher
than maximum inversion temperature is accompanied by decrease in
temperature of the gas. [IES-2003]
Reason (R): Joule-Kelvin coefficient μj is given ( ∂T / ∂p ) h and should have a
positive value for decrease in temperature during throttling process.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IES-20. Match List-I (Name of entity) with List-II (Definition) and select the correct
answer using the codes given below the lists: [IES-2001]
List-I (Name of entity) List-II (Definition)
Page 69 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
1 ⎛ ∂v ⎞
A. Compressibility factor 1. − ⎜ ⎟
v ⎝ ∂p ⎠T
⎛ ∂h ⎞
B. Joule – Thomson coefficient 2. ⎜ ⎟
⎝ ∂T ⎠ p
⎛ ∂T ⎞
C. Constant pressure specific heat 3. ⎜ ⎟
⎝ ∂p ⎠ h
⎛ pv ⎞
D. Isothermal compressibility 4. ⎜ ⎟
⎝ RT ⎠
Codes: A B C D A B C D
(a) 2 1 4 3 (b) 4 3 2 1
(c) 2 3 4 1 (d) 4 1 2 3
Page 70 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
(a) 4 2 1 3 (b) 1 2 4 3
(c) 4 1 2 3 (d) 2 1 4 3
Clausius-Clapeyron Equation
IES-24. Consider the following statements in respect of the Clausius – Clapeyron
equation: [IES-2007]
1. It points to one possible way of measuring thermodynamic temperature.
2. It permits latent heat of vaporization to be estimated from measurements of
specific volumes of saturated liquid, saturated vapour and the saturation
temperatures at two nearby pressures.
3. It does not apply to changes from solid to the liquid phase and from solid to
the Vapour phase.
Which of the statements given above are correct?
(a) 1, 2 and 3 (b) 1 and 2 only (c) 2 and 3 only (d) 1 and 3 only
IES-26. The variation of saturation pressure with saturation temperature for a liquid
is 0.1 bar/K at 400 K. The specific volume of saturated liquid and dry saturated
vapour at 400 K are 0.251 and 0.001 m3/kg What will be the value of latent heat
of vaporization using Clausius Clapeyron equation? [IES-2004]
(a) 16000 kJ/kg (b) 1600 kJ/kg (c) 1000 kJ/kg (d) 160 kJ/kg
IES-27. If h, p, T and v refer to enthalpy, pressure, temperature and specific volume
respectively and subscripts g and f refer to saturation conditions of vapour and
liquid respectively then Clausius-Clapeyron equation applied to change of
phase from liquid to vapour states is: [IES-1996, 2006]
dp (hg − h f ) dp (hg − h f )
(a) = (b) =
dt (vg − v f ) dt T (vg − v f )
dp (hg − h f ) dp (vg − v f )T
(c) = (d) =
dt T dt (hg − h f )
IES-28. Which one of the following functions represents the Clapeyron equation
pertaining to the change of phase of a pure substance? [IES-2002]
(a) f (T, p, hfg) (b) f (T, p, hfg, vfg) (c) f (T, p, hfg, sfg) (d) f (T, p, hfg, sfg, vfg)
IES-29. The Clapeyron equation with usual notations is given by: [IES-2000]
⎛ dT ⎞ h fg ⎛ dP ⎞ h fg ⎛ dT ⎞ Th fg ⎛ dP ⎞ Th fg
(a) ⎜ ⎟ = (b) ⎜ ⎟ = (c ) ⎜ ⎟ = (d ) ⎜ ⎟ =
⎝ dP ⎠sat Tv fg ⎝ dT ⎠ sat Tv fg ⎝ dP ⎠ sat v fg ⎝ dT ⎠ sat v fg
Page 71 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
IES-31. The thermodynamic parameters are: [IES-1997]
I. Temperature II. Specific Volume III. Pressure IV. Enthalpy V. Entropy
The Clapeyron Equation of state provides relationship between:
(a) I and II (b) II, III and V (c) III, IV and V (d) I, II, III and IV
IES-33. As per Gibb's phase rule, if number of components is equal to 2 then the
number of phases will be: [IES-2002]
(a) ≤ 2 (b) ≤ 3 (c) ≤ 4 (d) ≤ 5
IES-36. Which one of the following relationships defines the Helmholtz function F?
[IES-2007]
(a) F = H + TS (b) F = H – TS (c) F = U – TS (d) F = U +TS
IES-37. Assertion (A): For a mixture of solid, liquid and vapour phases of a pure
substance in equilibrium, the number of independent intrinsic properties
needed is equal to one. [IES-2005]
Reason(R): The Three phases can coexist only at one particular pressure.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
Page 72 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
Previous 20-Years IAS Questions
Maxwell's Equations
IAS-1. According to the Maxwell relation, which of the following is/are correct?
⎛ ∂v ⎞ ⎛ ∂s ⎞ ⎛ ∂s ⎞ ⎛ ∂P ⎞
(a) ⎜ ⎟ = −⎜ ⎟ (b) ⎜ ⎟ =⎜ ⎟ [IAS-2007]
⎝ ∂T ⎠ p ⎝ ∂P ⎠T ⎝ ∂v ⎠T ⎝ ∂T ⎠v
⎛ ∂P ⎞ ⎛ ∂s ⎞
(c) ⎜ ⎟ =⎜ ⎟ (d) All of the above
⎝ ∂T ⎠v ⎝ ∂v ⎠T
TdS Equations
IAS-2. Which one of the following expressions for T ds is true for a simple
compressible substance? (Notations have the usual meaning) [IAS-1998]
(a) dh – vdp (b) dh + vdp (c) dh – pdv (d) dh + pdv
⎡ ⎛ ∂s ⎞ ⎛ ∂s ⎞ ⎤
IAS-4. For an ideal gas the expression ⎢T ⎜ ⎟ −T ⎜ ⎟ ⎥ is always equal to:
⎣⎢ ⎝ ∂T ⎠ p ⎝ ∂T ⎠v ⎦⎥
cp
(a) zero (b) (c ) R (d ) RT [IAS-2003]
cv
IAS-5. Assertion (A): Specific heat at constant pressure for an ideal gas is always
greater than the specific heat at constant volume. [IAS-2000]
Reason (R): Heat added at constant volume is not utilized for doing any
external work.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IAS-6. Match List-I with List-II and select the correct answers using the codes given
below the lists. [IAS-2002]
List-I List-II
5
A. Joule Thomson co-efficient 1. R
2
B. Cp for monatomic gas 2. Cv
Page 73 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
C. Cp – Cv for diatomic gas 3. R
⎛ ∂U ⎞ ⎛ ∂T ⎞
D. ⎜ ⎟ 4. ⎜ ⎟
⎝ ∂T ⎠v ⎝ ∂P ⎠ h
Codes: A B C D A B C D
(a) 3 2 4 1 (b) 4 1 3 2
(c) 3 1 4 2 (d) 4 2 3 1
IAS-7. Ratio of specific heats for an ideal gas is given by (symbols have the usual
meanings) [IAS-1999]
1 1 1 1
(a) (b) (c) (d)
R C C R
1− 1− p 1+ p 1+
Cp R R Cp
Clausius-Clapeyron Equation
IAS-9. If h, p, T and v refer to enthalpy, pressure, temperature and specific volume
respectively and subscripts g and f refer to saturation conditions of vapour and
liquid respectively then Clausius-Clapeyron equation applied to change of
phase from liquid to vapour states is: [IAS-2003]
dp (hg − h f ) dp (hg − h f )
(a) = (b) =
dt (vg − v f ) dt T (vg − v f )
dp (hg − h f ) dp (vg − v f )T
(c) = (d) =
dt T dt (hg − h f )
IAS-10. Which one of the following is the correct statement? [IAS-2007]
Clapeyron equation is used for:
(a) Finding specific volume of vapour (b) Finding specific volume of liquid
(c) Finding latent heat of vaporization (c) Finding sensible heat
IAS-11. Assertion (A): Water will freeze at a higher temperature if the pressure is
increased. [IAS-2003]
Reason (R): Water expands on freezing which by Clapeyron's equation gives
negative slope for the melting curve.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
Page 74 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
IAS-12. Match List-I with List-II and select the correct answer using the codes given
below the lists [IAS-1994]
List-I List-II
A. Mechanical work 1. Clausius-Clapeyron equation
dQ
B. ∫ T
≤0 2. Gibb's equation
Page 75 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
Answers with Explanation (Objective)
Page 76 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
⎛ dT v.dp ⎞ ⎡ ∂ (1/ T ) ⎤ ⎡ ∂ ( −v / T ) ⎤ ⎡ ∂ (− R / P) ⎤
And for ∫ ⎜⎝ T −
T ⎠
⎟ ⎢ ∂p ⎥ = ⎢ ∂T ⎥ = ⎢ ∂T
⎣ ⎦T ⎣ ⎦P ⎣ ⎥⎦ or 0 = 0
P
⎛ dT v.dp ⎞
Thus ∫ ⎜⎝ T −
T ⎠
⎟ is exact and may be written as ds, where s is a point function and
hence a property
IES-2. Ans. (a) From Maxwell relation Clapeyron equation comes.
⎛ ∂p ⎞ ⎛ ∂s ⎞
IES-3. Ans. (b) 3 is false. It is derived from the Maxwell’s 3rd relationship ⎜ ⎟ =⎜ ⎟
⎝ ∂T ⎠v ⎝ ∂v ⎠T
IES-4. Ans. (a)
IES-5. Ans. (c) The relations in (a) and (b) are applicable for a reversible processes and (c) Tds = du
+ pdV is a relation among properties which are independent of the path.
IES-6. Ans. (b)
IES-7. Ans. (c)
IES-8. Ans. (a)
IES-9. Ans. (c) Potential energy will converted to heat energy.
gh 980 × 4000
mgh = mc v ΔT or ΔT = = = 40K
cv 980
IES-10. Ans. (b)
IES-11. Ans. (d) A diatomic gas (such as that of oxygen) has six degrees of freedom in all-three
corresponding to translator motion, two corresponding to rotatory motion and one
corresponding to vibratory motion. Experiments have shown that at ordinary
temperatures, the vibratory motion does not occur. Hence, at 27°C, an oxygen molecule
has just five degrees of freedom.
IES-12. Ans. (d)
IES-13. Ans. (a) Both A and R correct and R is the correct explanation of A
IES-14. Ans. (c). A is correct but R is false.
We know that C p = a+KT+K1T2+K2T3
C v = b+ KT+K1T2+K2T3
See Cp and C v both increase with temperature and by same amount. As Cp > C v then
C
percentage increase of Cp is less than C v. So p decreases with temperature.
Cv
⎛ ∂P ⎞
IES-15. Ans. (c) Sign of T must be positive ⎜ ⎟ is always negative.
⎝ ∂v ⎠T
IES-16. Ans. (a)
IES-17. Ans. (d) Actually Joule – Thomson coefficient will be positive.
IES-18. Ans. (c) For ideal gas µ = 0 and for real gas µ may be positive (N2, O2, CO2 etc.) or negative
(H2).
Page 77 of 121
Therm
T modyna
amic Relatio
R ons
S K Mo
ondal’s
s Cha
apter 6
IES-19. Ans. (d) When a real gas
whiich is initia
ally at a
tem
mperature lower than
the maximum inversion
mperature is throttled,
tem
its mperature
tem
deccreases.
IES-20. Ans. (b
b)
IES-21. Ans. (b)
( Joule Thhomson coeffiicient is the ratio of temperature cha
ange to presssure change
wheen a gas und
dergoes adiab
batic throttlin
ng.
IES-22. Ans. (a) The slope of the issenthalpic cu urve at any point is kn nown as Jouule-Thomson
⎛ ∂T ⎞
coeffficient and is
i expressed as,
a μ =⎜ ⎟
⎝ ∂p ⎠h
IES-23. Ans. (a
a)
IES-24. Ans. (b
b)
IES-25. Ans. (c
c)
⎛ dP ⎞ hfg
IES-26. Ans. (c
c) ⎜ ⎟ =
⎝ dT ⎠sat T ( Vg − Vf )
⎛ dP ⎞
or hfg = T ( Vg − Vf ) × ⎜ ⎟ = 400 × ( 0251 − 0.001) × 0.1× 10 J / kg = 1000kJ / kg
5
⎝ dT ⎠ sat
IES-27. Ans. (b
b)
IES-28. Ans. (b
b)
IES-29. Ans. (b
b)
IES-30. Ans. (c
c)
IES-31. Ans. (d) Clapeyrron equation n state proviides relation
nship betweeen temperatu ure, specific
voluume, pressurre and enthallpy.
IES-32. Ans. (d
d)
IES-33. Ans. (c
c)
IES-34. Ans. (d
d) F = C – P + 2
IES-35. Ans. (a)
( Gibb's fre ee energy 'G' is defined ass G = H – TS..
IES-36. Ans. (c
c)
IES-37. Ans. (d
d) F = C – P + 2
C = 1, P = 3 or F = 1 – 3 + 2 = 0
IES-38. Ans. (d) Isomers:: Compounds with the same s chemiccal formula but differen nt molecular
struucture.
Page 78 of 121
Thermodynamic Relations
S K Mondal’s Chapter 6
Previous 20-Years IAS Answers
⎛ ∂P ⎞ ⎛ ∂S ⎞
IAS-1. Ans. (c) ⎜ ⎟ =⎜ ⎟ to memorize Maxwell’s relation remember T V P S, –ive and S S V
⎝ ∂T ⎠V ⎝ ∂V ⎠T
P see highlights.
IAS-2. Ans. (a) dQ = dh – Vdp or Tds = dh – Vdp
dQp ⎛ ∂s ⎞
IAS-3. Ans. (c) Cp = = T⎜ ⎟ [∵ dQ = TdS]
∂T ⎝ ∂T ⎠p
IAS-4. Ans. (c)
⎛ ∂S ⎞ ⎛ T∂S ⎞ ⎛ dQ ⎞
T⎜ ⎟ =⎜ ⎟ =⎜ ⎟ = CP
⎝ ∂T ⎠P ⎝ ∂T ⎠P ⎝ ∂T ⎠P
⎛ ∂S ⎞ ⎛ T∂S ⎞ ⎛ dQ ⎞
T⎜ ⎟ =⎜ ⎟ =⎜ ⎟ = CV
⎝ ∂T ⎠ V ⎝ ∂T ⎠ V ⎝ ∂T ⎠ V
⎛ ∂S ⎞ ⎛ ∂S ⎞
∴T⎜ ⎟ − T ⎜ ∂T ⎟ = CP − CV = R
⎝ ∂T ⎠P ⎝ ⎠V
IAS-5. Ans. (a) Both A and R correct and R is the correct explanation of A
IAS-6. Ans. (b) Cp – Cv for all ideal gas is R, So C-3, (a) & (c) out. A automatically match 4, and
γ 5 5
Cp = R for monatomic gas γ = . So, γ = R.
γ −1 3 2
Cp Cp 1
IAS-7. Ans. (a) Cp − Cv = R and γ = = =
Cv Cp − R R
1−
Cp
IAS-8. Ans. (b)
IAS-9. Ans. (b)
IAS-10. Ans. (c)
IAS-11. Ans. (a)
IAS-12. Ans. (d)
IAS-13. Ans. (b)
IAS-14. Ans. (b)
Page 79 of 121
Pure Substances
S K Mondal’s Chapter 7
7. Pure Substances
Specific volumes of liquid (vf) and vapour (vg) phases, as well as values of saturation
temperatures, are given in the table below.
Pressure (kPa) Saturation temperature, vf(m3/kg) vg(m3/kg)
Tsat (°C)
100 100 0.001 0.1
200 200 0.0015 0.002
GATE-1. At the end of the process, which one of the following situations will be true?
(a) Superheated vapour will be left in the system [GATE-2008]
(b) No vapour will be left in the system
(c) A liquid + vapour mixture will be left in the system
(d) The mixture will exist at a dry saturated vapour state
GATE-2. The work done by the system during the process is: [GATE-2008]
(a) 0.1 kJ (b) 0.2 kJ (c) 0.3 kJ (d) 0.4kJ
Page 80 of 121
Pu
ure Su
ubstan
nces
S K Mo
ondal’s
s Cha
apter 7
GA
ATE-3. The e net entropy generatiion (considering the syystem and the
t thermal reservoir
tog
gether) duriing the proc
cess is close
est to: GATE-2008]
[G
(a) 7.5 J/K (b) 7.7 J/K (c)) 8.5 J/K (d) 10 J/K
T-
T-s Diagram for a Pure
e Substance
Co
ommon Data for Qu
uestions GATE-4
G - GA
ATE-5
A tthermodyna
amic cycle with
w an ideal gas as wo
orking fluid
d is shown below.
b
ATE-4.
GA The
e above cyc
cle is repressented on T--S plane by ATE-2007]
[GA
ATE-5.
GA If the
t specific heats of th he working fluid are coonstant and d the value of specific
heaat ratio γ is 1.4, the the
ermal efficie
ency (%) of the cycle iss: [G
GATE-2007]
Page 81 of 121
Pure Substances
S K Mondal’s Chapter 7
(a) 21 (b) 40.9 (c) 42.6 (d) 59.7
GATE-6. The slopes of constant volume and constant pressure lines in the T-s diagram
are….. and….. respectively. [GATE-1994]
Throttling
Statement for Linked Answer Questions Q9 & Q10:
The following table of properties was printed out for saturated liquid and saturated
vapour of ammonia. The titles for only the first two columns are available. All that we
know is that the other columns (columns 3 to 8) contain data on specific properties,
namely, internal energy (kJ/kg), enthalpy (kJ/kg) and entropy (kJ/kgK) [GATE-2005]
GATE-10. When saturated liquid at 40°C is throttled to -20°C, the quality at exit will be
[GATE-2005]
(a) 0.189 (b) 0.212 (c) 0.231 (d) 0.788
GATE-11. When wet steam flows through a throttle valve and remains wet at exit
(a) its temperature and quality increases [GATE-1996]
(b) its temperature decreases but quality increases
(c) its temperature increases but quality decreases
(d) its temperature and quality decreases
GATE-12. When an ideal gas with constant specific heats is throttled adiabatically, with
negligible changes in kinetic and potential energies [GATE-2000]
(a ) Δh = 0, ΔT = 0 (b) Δh > 0, ΔT = 0 (c) Δh > 0, ΔS > 0 (d ) Δh = 0, ΔS > 0
Page 82 of 121
Pu
ure Su
ubstan
nces
S K Mo
ondal’s
s Cha
apter 7
Whhere h, T and
a S reprresent respeectively, entthalpy, temp
perature an
nd entropy,
tem
mperature an
nd entropy
Previo
ous 20
0-Years
s IES Questi
Q ions
IES-1. Asssertion (A): Water is no ot a pure suubstance. [IES-1999]
Reaason (R): The term pure subsstance dessignates a substance which is
hommogeneous and has the e same chem mical composition in all
a phases.
(a) Both A and R are individ dually true and
a R is the correct
c explan
nation of A
(b) Both A and R are individ dually true but
b R is NOTT the correct explanation
e o A
of
(c) A is true buut R is false
(d) A is false bu
ut R is true
[IES-1998]
[IES-1997]
Page 83 of 121
Pu
ure Su
ubstan
nces
S K Mo
ondal’s
s Cha
apter 7
IES-5. Whhich one of the following systems can be con
nsidered to be contain
ning a pure
sub
bstance? [IES-1993]
p–
–v Diag
gram fo
or a Purre Subs
stance
IES-10. Wh
hich p–v diiagram for steam illu ustrates co e isothermal process
orrectly the
und
dergone by wet steam till it becom
mes superhe
eated? [IES 1995, 2007]
Page 84 of 121
Pu
ure Su
ubstan
nces
S K Mo
ondal’s
s Cha
apter 7
p–
–T Diag
gram fo
or a Purre Subs
stance
IES-11. Connsider the e phase diagram off a
cer
rtain substtance as shown in the t
giv
ven figure. Match List-I (Proce ess)
witth List-II (Curves/linees) and select
the
e correct answer
a usin
ng the cod
des
giv
ven below thhe lists:
Lisst-I List--II
(Prrocess) (Currves/lines)
A. Vaporization
n 1. EF
F
B. Fusion 2. EG
G
n
C. Sublimation 3. ED
D
[
[IES-2001]
des:
Cod A B C A B C
(a) 1 3 2 (b) 1 2 3
(c) 3 2 1 (d) 3 1 2
Page 85 of 121
Pure Substances
S K Mondal’s Chapter 7
p-v-T Surface
IES-12. The p-v-T surface of a pure
substance is shown in the
given p figure. The two-phase
regions are labelled as:
(a) R, T and X
(b) S, U and W
(c) S, W and V
(d) R, T and V
[IES-1999]
Page 86 of 121
Pu
ure Su
ubstan
nces
S K Mo
ondal’s
s Cha
apter 7
IES-14. The e followin ng figure shows th he T-s
dia
agram for steam.
s With h respect tot this
figuure, match List I with List II and select
thee correct annswer using g the codess given
bellow the Listts:
Lisst-I List-II
A. Curve
C I 1. Satu urated liquid line
B. Curve
C II 2. Satu urated vapourr line
C. Curve
C III 3. Consstant pressurre line
D. Curve
C IV 4. Consstant volume line [IES-1994]
Cod des: A B C D A B C D
(a) 2 1 4 3 (b) 2 1 3 4
(c) 1 2 3 4 (d) 1 2 4 3
C
Critical Point
P
IES-15. Wh hich one of the
t followin
ng is correct? [
[IES-2008]
At critical point the enthalpy of vapoorization iss
n temperaturre only
(a) dependent on (b)) maximum
(c) minimum
m (d)) zero
Page 87 of 121
Pure Substances
S K Mondal’s Chapter 7
IES-19. With increase of pressure, the latent heat of steam [IES-2002]
(a) Remains same (b) Increases (c) Decreases (d) Behaves unpredictably
IES-20. List-I gives some processes of steam whereas List-II gives the effects due to the
processes. Match List I with List II, and select the correct answer using the
codes given below the lists: [IES-1995]
List-I List-II
A. As saturation pressure increases 1. Entropy increases.
B. As saturation temperature increases 2. Specific volume increases.
C. As saturation pressure decreases 3. Enthalpy of evaporation decreases.
D. As dryness fraction increases 4. Saturation temperature increases.
Code: A B C D A B C D
(a) 1 3 2 4 (b) 4 3 2 1
(c) 4 3 1 2 (d) 2 4 3 1
IES-23. Consider the following statements regarding the throttling process of wet
steam: [IES-2002]
1. The steam pressure and temperature decrease but enthalpy remains
constant.
2. The steam pressure decreases, the temperature increases but enthalpy
remains constant.
3. The entropy, specific volume, and dryness fraction increase.
4. The entropy increases but the volume and dryness fraction decrease.
Which of the above statements are correct?
(a) 1 and 4 (b) 2 and 3 (c) 1 and 3 (d) 2 and 4
IES-24. Match List-I (Apparatus) with List-II (Thermodynamic process) and select the
correct answer using the code given below the Lists: [IES-2006]
List-I List-II
A. Separating calorimeter 1. Adiabatic process
B. Throttling calorimeter 2. Isobaric process
C. Sling psychrometer 3. Isochoric process
D. Gas thermometer 4. Isenthalpic process
Codes: A B C D A B C D
Page 88 of 121
Pu
ure Su
ubstan
nces
S K Mo
ondal’s
s Cha
apter 7
(a) 1 3 2 4 (b) 2 4 1 3
(c) 1 4 2 3 (d) 2 3 1 4
IES-25. Sellect the corrrect answerr using the codes given n below the Lists: [IES-1998]
List-I List-III
A. Bomb caloriimeter 1. Pressure
B. Exhaust gass calorimeterr 2. Enthallpy
C. Junker gas calorimeter 3. Volumee
D. Throttling calorimeter
c 4. Specific heats
Codde: A B C D A B C D
(a) 3 4 1 2 (b) 2 4 1 3
(c) 3 1 4 2 (d) 4 3 2 1
Throttlin
ng
IES-26. In a throttlinng processs, which on ne of the following parameterrs remains
connstant? [IES-2009]
(a) Temperature
e (b) Pressure (c)) Enthalpy (d) Entropy
E
[IIES-2000]
IES-29. A fluid
fl flowing
g along a piipe line und
dergoes a th hrottling process from 10 bar to 1
Bar r in passing through a partially open valve e. Before th hrottling, th
he specific
vollume of the fluid is 0.5 m3 /kg and after throtttling is 2.0 m3 /kg. Whatt is the
Change in spe ecific internnal energy during
d the throttling
t process? [IES 2007]
(a) Zero (b) 100
0 kJ/kg (c) 200 kJ//kg kg
(d) 300 kJ/k
Page 89 of 121
Pure Substances
S K Mondal’s Chapter 7
IES-30. The throttling process undergone
by a gas across an orifice is shown
by its states in the following figure:
[IES-1996]
[IES-1992]
IES-32. Match List-l with List-Il and select the correct answer using the code given
below the lists: [IES-2009]
List-l List-lI
A. Isolated system 1. Energy is always constant
B. Nozzle 2. Increase in velocity at the expense of its
C. Throttling device pressure drop
D. Centrifugal compressor 3. Appreciable drop in pressure without any
change in energy
4. Enthalpy of the fluid increases by the amount
of work input
Codes: A B C D A B C D
(a) 4 3 2 1 (b) 1 3 2 4
(c) 4 2 3 1 (d) 1 2 3 4
Page 90 of 121
Pu
ure Su
ubstan
nces
S K Mo
ondal’s
s Cha
apter 7
Previo
ous 20
0-Years
s IAS Quest
Q ions
IA
AS-1. Whhich one of the following systems can be con
nsidered to be contain
ning a pure
sub
bstance? [IAS 1998]
AS-2.
IA Asssertion (A): On the enthalpy-en
e ntropy diag gram of a pure subsstance the
connstant dryn ness fraction n lines startt from the critical
c poinnt. [IAS-2001]
Reaason (R): Alll the three phases co-e exist at the critical point.
(a) Both A and R are individ dually true and
a R is the correct
c explannation of A
(b) Both A and R are individ dually true but
b R is NOT T the correct explanation
e o A
of
(c) A is true buut R is false
(d) A is false bu
ut R is true
AS-3.
IA Asssertion (A): Air, a mixtu ure of O2 annd N2, is a pure substan nce. [IAS-2000]
Reaason(R): Air is homo ogeneous in composition and uniform u in
n chemical
agggregation.
(a) Both A and R are individ dually true and
a R is the correct
c explannation of A
(b) Both A and R are individ dually true but
b R is NOT T the correct explanation
e o A
of
(c) A is true buut R is false
(d) A is false bu
ut R is true
AS-4.
IA If a pure substance conta ained in a rigid
r vessel passes throough the critical state
on heating, itss initial statte should be
e: [IAS-1998]
(a) Subcooled water (b) Saturated
d water (c)) Wet steam (d) Saturateed steam
AS-5.
IA Asssertion (A): Air is a pu ure substan nce but a mixture
m of air
a and liqu uid air in a
cylinder is nott a pure sub bstance. [IAS-1996]
Reaason (R): Aiir is homog geneous in composition
c n but a mix xture of air and liquid
air is heteroge eneous.
(a) Both A and R are individ dually true and
a R is the correct
c explan
nation of A
(b) Both A and R are individ dually true but
b R is NOTT the correct explanation
e o A
of
(c) A is true buut R is false
(d) A is false bu
ut R is true
Page 91 of 121
Pu
ure Su
ubstan
nces
S K Mo
ondal’s
s Cha
apter 7
IA
AS-6. Asssertion (A): Temperatu ure and pressure are sufficient to o fix the statte of a two
phaase system. [IAS-1995]
Reaason(R): Tw wo indepen ndent and intensive properties are requiired to be
knoown to defin ne the state e of a pure substance.
s
(a) Both A and R are individ dually true and
a R is the correct
c explan
nation of A
(b) Both A and R are individ dually true but
b R is NOTT the correct explanation
e o A
of
(c) A is true buut R is false
(d) A is false bu
ut R is true
p–
–v Diag
gram fo
or a Purre Subs
stance
IA
AS-7. Twwo-phase regions
r in
n the given
g
preessure-volumme diagraam of a pure
subbstance are represente
ed by
(a) A,
A E and F
(b) B, C and D
(c) B,
B D and F
(d) A, C and E
[IAS-1999]
AS-8.
IA A cyclic
c proce
ess ABC is shown
s on a V–T
dia
agram in fig
gure.
Thee same proc
cess on a P––V diagram
m will
be represent as:
a
[
[IAS-1996]
Page 92 of 121
Pure Substances
S K Mondal’s Chapter 7
IAS-9. The network done for the
closed shown in the given
pressure-volume diagram, is
(a) 600kN-m (b) 700kN-m
(c) 900kN-m (d) 1000kN-m
[IAS-1995]
Triple point
IAS-10. Triple point temperature of water is: [IAS-2000]
(a) 273 K (b) 273.14 K (c) 273.15K (d) 273.16 K
[IAS-1998]
Page 93 of 121
Pure Substances
S K Mondal’s Chapter 7
IAS-13. Two heat engine cycles (l - 2 -
3 - 1 and l' - 2' - 3' - l’) are
shown on T-s co-ordinates in
[IAS-1999]
[IAS-1999]
Page 94 of 121
Pure Substances
S K Mondal’s Chapter 7
IAS-15. The given figure shows a thermodynamic
cycle on T-s diagram. All the processes
are straight times. The efficiency of the
cycle is given by
(a) (0.5 Th – Te)/ Th
(b) 0.5 (Th – Te)/ Th
(c) (Th – Te)/ 0.5 Th
(d) (Th – 0.5 Te)/ Th
[IAS-1996]
IAS-17. Assertion (A): In Mollier chart for steam, the constant pressure lines are
straight lines in wet region.
Reason (R): The slope of constant pressure lines in wet region is equal to T.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is not the correct explanation of A
(c) A is true but R is false [IAS-1995]
(d) A is false but R is true
Throttling
IAS-19. Assertion (A): Throttle governing is thermodynamically more efficient than
nozzle control governing for steam turbines. [IAS-2000]
Reason (R): Throttling process conserves the total enthalpy.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
Page 95 of 121
Pu
ure Su
ubstan
nces
S K Mo
ondal’s
s Cha
apter 7
Answ
wers with Expla
anatio
on (Ob
bjectiv
ve)
Previo
ous 20-Years
s GATE
E Answ
wers
GA
ATE-1. Ans. (a) Initial Volume
V 3 × 0.1 m3 = 0.004
(V1) = 0.001 + 0.03 0 m3
Lett dryness fracction = x
Theerefore 0.0044 × 1.5 = (1 – x) × 0.0015 × 1.03 + x × 0.002 × 1.003
Thaat gives an absurd value of x = 8.65 (IIt must be leess than equa
al to unity). So
S vapour is
sup
perheated.
ATE-2. Ans. (d) Work do
GA one = first con
nstant volum
me heating + ∫ pdv
= 0 + P (V2-V1) = 200 × (0.006-0.004) = 0.4 kJ
10000
ATE-3. Ans. (c) ( ΔS = (Δ
GA ΔS ) syatem + ( ΔS ) surroundings = 10 – = 8.51 J/K
(273 + 400)
GA
ATE-4. Ans. (c)
GA
ATE-5. Ans. (b)
GA
ATE-6. Ans.. Higher, Lowwer
GA
ATE-7. Ans. (a) Mollier diagram
d is a h-s plot.
⎛ ∂h ⎞
= T = slope
Tdss= dh - υ dp orr ⎜⎝ ∂s ⎟⎠ P
GA
ATE-9. Ans. (d)
Page 96 of 121
Pure Substances
S K Mondal’s Chapter 7
GATE-12. Ans. (d)
Δh = o
Δs > 0
ΔT < 0
T2 P
GATE-13. Ans. (a) S2 − S1 = C pav ln − Ru ln 2
T1 P1
P2
Change in entropy of the universe = − Ru ln
P1
0.1 kJ
= −8.314 ln = 13.38
0.5 K
For an ideal gas change in enthalpy is a function of temperature alone and change in
enthalpy of a throttling process is zero.
Page 97 of 121
Pure Substances
S K Mondal’s Chapter 7
IES-12. Ans. (c)
IES-13. Ans. (a)
IES-14. Ans. (c)
IES-15.Ans.(d) Characteristics of the critical point
1. It is the highest temperature at which the liquid and vapour phases can coexist.
2. At the critical point hfg, ufg and vfg are zero.
3. Liquid vapour meniscus will disappear.
4. Specific heat at constant pressure is infinite.
IES-16. Ans. (d) At critical point, the latent heat in zero and steam generators can operate above
this point as in the case of once through boilers.
The density of liquid and its vapour is however same and thus statement 2 is wrong.
IES-17. Ans. (b)
IES-18. Ans. (b)
IES-19. Ans. (c)
IES-20. Ans. (c)
IES-21. Ans. (b) ⎛ ∂h ⎞
Tds = dh – Vdp or ⎜ ∂s ⎟ = T
⎝ ⎠P
The slope of the isobar on the h–s diagram is
equal to the absolute temp, for condensation
T is cost so slope is const, but not zero so it is
inclined line.
Page 98 of 121
Pure Substances
S K Mondal’s Chapter 7
IES-27. Ans. (b) Temperature decreases and the
steam becomes superheated.
Page 99 of 121
Pure Substances
S K Mondal’s Chapter 7
h fg 1800
IAS-12. Ans. Sg = S f + = 2.6 + = 6.2 kJ / kgK
Tsat 500
IAS-13. Ans. (d)
1
IAS-14. Ans. (a) Work (W) = ( 0.03 − 0.01) × ( 400 − 200 ) + × ( 600 − 400 ) × ( 0.03 − 0.01) = 6kJ
2
W 6
W = pm × ΔV or pm = = kPa = 3bar
ΔV ( 0.03 − 0.01)
1
IAS-15. Ans. (b) Work output = Area 123 = × ( Th − Tc ) × ( S2 − S1 )
2
Heat added = Area under 1 − 2 = Th ( S2 − S1 )
1
( Th − Tc )( S2 − S1 )
∴η = 2 = 0.5 ( Th − Tc ) / Th
Th ( S2 − S1 )
IAS-16. Ans. (a) Mollier diagram is a h-s plot.
⎛ ∂h ⎞
Tds= dh – υ dp or ⎜ ⎟ = T = slope
⎝ ∂s ⎠ P
T is always + ive so slope always +ive. Not only this if T ↑ then slope ↑
IAS-17. Ans. (a) Both A and R are true and R is the correct explanation of A
IAS-18. Ans. (d)
IAS-19. Ans. (d) If throttle governing is done at low loads, the turbine efficiency is considerably
reduced. The nozzle control may then be a better method of governing.
Adiabatic Process
GATE-2. A mono-atomic ideal l gas (γ = 1.67, molecular weight = 40) is compressed
adiabatically from 0.1 MPa, 300 K to 0.2 MPa. The universal gas constant is
8.314 kJ kmol-1K-1. The work of compression of the gas (in kJ kg-1) is:
[GATE-2010]
(a) 29.7 (b) 19.9 (c) 13.3 (d) 0
GATE-3. The amount of heat lost by the air in the football and the gauge pressure of air
in the football at the stadium respectively equal [GATE-2006]
(a) 30.6 J, 1.94 bar (b) 21.8 J, 0.93 bar (c) 61.1 J, 1.94 bar (d) 43.7 J, 0.93 bar
GATE-4. Gauge pressure of air to which the ball must have been originally inflated so
that it would equal 1 bar gauge at the stadium is: [GATE-2006]
(a) 2.23 bar (b) 1.94 bar (c) 1.07 bar (d) 1.00 bar
Isothermal Process
GATE-6. A frictionless piston-cylinder device contains a gas initially at 0.8 MPa and
0.015 m3. It expands quasi-statically at constant temperature to a final volume
of 0.030 m3. The work output (in id) during this process will be: [GATE-2009]
(a) 8.32 (b) 12.00 (c) 554.67 (d) 8320.00
Avogadro's Law
IES-1. Assertion (A): The mass flow rate through a compressor for various
refrigerants at same temperature and pressure, is proportional to their
molecular weights. [IES-2002]
Reason (R): According to Avogardo’s Law all gases have same number of moles
in a given volume of same pressure and temperature.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is NOT the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
Ideal Gas
IES-2. Assertion (A): A perfect gas is one that satisfies the equation of state and whose
specific heats are constant. [IES-1993]
Reason (R): The enthalpy and internal energy of a perfect gas are functions of
temperature only.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is not the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IES-8. If a real gas obeys the Clausius equation of state p(v – b) = RT then, [IES-1992]
⎛ ∂u ⎞ ⎛ ∂u ⎞ ⎛ ∂u ⎞ ⎛ ∂u ⎞ 1
(a) ⎜ ⎟ ≠0 (b) ⎜ ⎟ =0 (c) ⎜ ⎟ = 1 (d) ⎜ ⎟ =
⎝ ∂v ⎠T ⎝ ∂v ⎠T ⎝ ∂v ⎠T ⎝ ∂v ⎠T p
IES-11. Which of the following statement about Van der waal's equation i valid?
(a) It is valid for all pressure and temperatures [IES-1992]
(b) It represents a straight line on pv versus v plot
(c) It has three roots of identical value at the critical point
(d) The equation is valid for diatomic gases only.
IES-12. The internal energy of a gas obeying Van der Waal’s equation
⎛ a⎞
⎜ P + 2 ⎟ ( v − b ) = RT , depends on [IES-2000]
⎝ v ⎠
(a) Temperature (b) Temperature and pressure
(c) Temperature and specific volume (d) Pressure and specific volume
⎛ a⎞
IES-13. Van der Waal’s equation of state is given by ⎜ P + 2 ⎟ ( v − b ) = RT . The constant
⎝ v ⎠
‘b’ in the equation in terms of specific volume at critical point Vc is equal to:
[IES-2003]
8a
(a) Vc/3 (b) 2 Vc (c) 3 Vc (d)
27VcR
Compressibility
IES-14. Consider the following statements: [IES-2007]
1. A gas with a compressibility factor more than 1 is more compressible than a
perfect gas.
2. The x and y axes of the compressibility chart are compressibility factor on
y-axis and reduced pressure on x-axis.
3. The first and second derivatives of the pressure with respect to volume at
critical points are zero.
Which of the statements given above is/are correct?
(a) 2 and 3 only (b) 1 and 3 only (c) 1 and 2 only (d) 1, 2 and 3
IES-16. Assertion (A): At very high densities, compressibility of a real gas is less than
one. [IES-2006]
Reason (R): As the temperature is considerably reduced, the molecules are
brought closer together and thermonuclear attractive forces become greater at
pressures around 4 MPa.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is not the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IES-17. The value of compressibility factor for an ideal gas may be: [IES-2002]
1. less or more than one 2. equal to one 3. zero 4. less than zero
The correct value(s) is/are given by:
(a) 1 and 2 (b) 1 and 4 (c) 2 only (d) 1 only
IES-18. Assertion (A): The value of compressibility factor, Z approaches zero of all
isotherms as pressure p approaches zero. [IES-1992]
Reason (R): The value of Z at the critical points is about 0.29.
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is not the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
Adiabatic Process
IES-19. Assertion (A): An adiabatic process is always a constant entropy process.
Reason(R): In an adiabatic process there is no heat transfer. [IES-2005]
(a) Both A and R are individually true and R is the correct explanation of A
(b) Both A and R are individually true but R is not the correct explanation of A
(c) A is true but R is false
(d) A is false but R is true
IES-22. A balloon which is initially collapsed and flat is slowly filled with a gas at 100
kPa so as to form it into a sphere of 1 m radius. What is the work done by the
gas in the balloon during the filling process? [IES-2008]
(a) 428·9 kJ (b) 418·9 kJ (c) 420·9 kJ (d) 416·9 kJ
Isothermal Process
IES-23. An ideal gas undergoes
an isothermal
expansion from state R
to state S in a turbine
as shown in the
diagram given below:
The area of shaded
region is 1000 Nm. What
is the amount is turbine
work done during the
process? [IES-2004]
(a) 14,000 Nm (b) 12,000 Nm (c) 11,000Nm (d) 10,000Nm
IES-26. The work done during expansion of a gas is independent of pressure if the
expansion takes place [IES-1992]
(a) Isothermally (b) Adiabatically
(c) In both the above cases (d) In none of the above cases
IES-27. Three moles of an ideal gas are compressed to half the initial volume at a
constant temperature of 300k. The work done in the process is [IES-1992]
(a) 5188 J (b) 2500 J (c) –2500 J (d) –5188 J
IES-31. The heat absorbed or rejected during a polytropic process is equal to:
1/2
⎛γ −n⎞ ⎛γ −n⎞
(a) ⎜ ⎟ x work done (b) ⎜ ⎟ x work done [IES-2002]
⎝ γ −1 ⎠ ⎝ n −1 ⎠
⎛γ −n⎞
2
⎛γ −n⎞
(c) ⎜ ⎟ x work done (d ) ⎜ ⎟ x work done
⎝ γ −1 ⎠ ⎝ γ −1 ⎠
IES-33. Which one of the following phenomena occurs when gas in a piston-in-cylinder
assembly expands reversibly at constant pressure? [IES-2003]
(a) Heat is added to the gas
(b) Heat is removed from the gas
(c) Gas does work from its own stored energy
(d) Gas undergoes adiabatic expansion
IES-34. A saturated vapour is compressed to half its volume without changing its
temperature. The result is that: [IES-1997]
(a) All the vapour condenses to liquid
(b) Some of the liquid evaporates and the pressure does not change
(c) The pressure is double its initial value
(d) Some of the vapour condenses and the pressure does not change
IES-35. An ideal gas at 27°C is heated at constant pressure till its volume becomes
three times. [IES-2008]
What would be then the temperature of gas?
(a) 81° C (b) 627° C (c) 543° C (d) 327° C
IES-39. Match List-I (process) with List-II (index n in PVn = constant) and select the
correct answers using the codes given below the lists. [IES-1999]
List-I List-II
A. Adiabatic 1. n = infinity
B. Isothermal 2. n = C p
Cv
C. Constant pressure 3. n = 1
D. Constant volume 4. n = C p -1
Cv
5. n = zero
Codes: A B C D A B C D
(a) 2 3 5 4 (b) 3 2 1 5
(c) 2 3 5 1 (d) 2 5 3 1
IES-40. A system at a given state undergoes change through the following expansion
processes to reach the same final volume [IES-1994]
1. Isothermal 2. Isobaric
3. Adiabatic ( γ = 1.4) 4. Polytropic(n =1.3)
The correct ascending order of the work output in these four processes is
IES-41. Match the curves in Diagram-I with the curves in Diagram-II and select the
correct answer. [IES-1996]
Diagram-I (Process on p-V plane) Diagram-II (Process on T-s plane)
Code: A B C D A B C D
(a) 3 2 4 5 (b) 2 3 4 5
(c) 2 3 4 1 (d) 1 4 2 3
IES-42.
Four processes of a thermodynamic cycle are shown above in Fig.I on the T-s
plane in the sequence 1-2-3-4. The corresponding correct sequence of these
processes in the p- V plane as shown above in Fig. II will be [IES-1998]
(a) C–D–A–B (b) D–A–B–C (c) A–B–C–D (d) B–C–D–A
IES-43. Match List-I with List-II and select the correct answer [IES-1996]
List-I List-II
A. Work done in a polytropic process 1. − ∫ vdp
B. Work done in a steady flow process 2. Zero
p1V1 − p2V2
C. Heat transfer in a reversible adiabatic process 3.
γ −1
p1V1 − p2V2
D. Work done in an isentropic process 4.
n −1
Codes: A B C D A B C D
(a) 4 1 3 2 (b) 1 4 2 3
(c) 4 1 2 3 (d) 1 2 3 4
IES-44. A perfect gas at 27°C was heated until its volume was doubled using the
following three different processes separately [IES-2004]
Ideal Gas
IAS-1. Variation of pressure and volume at constant temperature are correlated
through [IAS-2002]
(a) Charles law (b) Boyle’s law (c) Joule’s Law (d) Gay Lussac’s Law
IAS-4. An ideal gas with initial volume, pressure and temperature of 0.1 m3, 1bar and
27°C respectively is compressed in a cylinder by a piston such that its final
volume and pressure are 0.04 m3 and 5 bars respectively, then its final
temperature will be: [IAS-2001]
(a) –123°C (b) 54°C (c) 327°C (d) 600°C
IAS-6. An Ideal gas with initial volume, pressure and temperature of 0.1m3, 1 bar and
27°C respectively is compressed in a cylinder by piston such that its final
volume and pressure 0.04 m3 and 5 bar respectively, then its final temperature
will be: [IAS-2001]
(a) –123°C (b) 54°C (c) 327°C (d)600°C
IAS-7. Which one of the following PV-T diagrams correctly represents the properties
of an ideal gas? [IAS-1995]
Critical Properties
IAS-11. The mathematical conditions at the critical point for a pure substance are
represented by: [IAS-1999]
δp δ2p δ3p δp δ2p δ3p
(a) < 0, 2 = 0 and 3 = 0 (b) = 0, 2 < 0 and 3 = 0
δv δv δv δv δv δv
δp δ p
2
δ3p δp δ p
2
δ3p
(c) = 0, 2 = 0 and 3 < 0 (d) = 0, 2 = 0 and 3 = 0
δv δv δv δv δv δv
Adiabatic Process
IAS-13. Consider the following statements: [IAS-2007]
1. During a reversible non-flow process, for the same expansion ratio, work
done by a gas diminishes as the value of n in pvn = C increases.
2. Adiabatic mixing process is a reversible process.
Which of the statements given above is/are correct?
(a) 1 only (b) 2 only (c) Both 1 and 2 (d) Neither 1 nor 2
Isothermal Process
IAS-14. Identify the process of change of a close system in which the work transfer is
maximum. [IAS-2003]
(a) Isothermal (b) Isochoric (c) Isentropic (d) Polytrop
IAS-15. In a reversible isothermal expansion process, the fluid expands from 10 bar
and 2 m3 to 2 bar and 10 m3. During the process the heat supplied is at the rate
of 100 kW. What is the rate of work done during the process? [IAS-2007]
(a) 20 kW (b) 35 kW (c) 80 kW (d) 100 kW
IAS-20. Match List-I with List-II and select the correct answer using the codes given
below the Lists: [IAS-1997]
List-I List- II
dP P
A. Constant volume process 1. =−
dV V
dP γP
B. Constant pressure process 2. =−
dV V
dT T
C. Constant temperature process 3. =−
ds Cv
dT T
D. Constant entropy process 4. =−
ds CP
Codes: A B C D A B C D
(a) 3 2 1 4 (b) 2 4 3 1
(c) 3 4 1 2 (d) 1 3 4 2
10
( )
= 4 π13 (100 ) = 418.9 kJ
3
IES-23. Ans. (c) Turbine work = area under curve R–S = ∫ P dv
= 1 bar × ( 0.2 − 0.1) m3 + 1000 Nm
= 105 × ( 0.2 − 0.1) Nm + 1000Nm = 11000Nm
IES-24. Ans. (b)
IES-25. Ans. (a) PV = constant, C
⇒ log P + log V = log C
m1 = -1
Pv 4 = C
⇒ log P + q log V = log C
m2 = -q = - 1.4
∴ m2 > m1
IES-26. Ans. (d)
IES-27. Ans. (d) Since the temperature remains constant, the process is isothemal.
⎛V ⎞
∴ Work-done in the process, W = 2.303 nRT log ⎜ 2 ⎟
⎝ V1 ⎠
⎛1 ⎞
= 2.303 х 3 х 8.315 х 8.315 х 300 log ⎜ ⎟
⎝2⎠
= – 5188 J.
The negative sign indicates that work is done on the gas.
IES-28. Ans. (b) Tds = du + pdv
⇒ Τds = C V dT + pdv
dT P
⇒ ds = CV + dv
T T
dT R
⇒ ds = CV + dv
T V
Integrating the above expression
T2 V
⇒ S2 − S1 = C V In + RIn 2
T1 V1
For isothermal process undergone by ideal gas.
V2
⇒ S2 − S1 = ( CP − CV ) In
V1
IES-29. Ans. (a)
IES-30. Ans. (a)
IES-31. Ans. (c)
IES-32. Ans. (c) dQ = du + pdυ + υ pd − υ dp = d ( u + pυ ) − υ dp = dh − υ dp
if dp = 0 or p = const. these for ( dQ )p = ( dh )p
IES-34. Ans. (d) By compressing a saturated vapour, its vapours condense and pressure remains
unchanged. Remember it is not gas.
V V V1 3V1
IES-35. Ans. (b) 1 = 2 ⇒ =
T1 T2 ( 273 + 27 ) T2
⇒ T2 = 300 × 3 = 900 K = 627°C
IES-36. Ans. (a) Constant volume (isochoric) process: An example of this process is the heating
or cooling of a gas stored in a rigid cylinder. Since the volume of the gas does not change,
no external work is done, and work transferred ΔW is zero. Therefore from 1st law of
thermodynamics for a constant volume process:
W2 = 0
1
2
1Q 2 = ∫ dU = U2 − U1
1
IES-37. (c) In a pressure cooker, the volume of the cooker is fixed so constant volume process but for
safety some of steam goes out to maintain a maximum pressure. But it occurs after
proper steaming.
IES-38. Ans. (b)
IES-39. Ans. (c)
IES-40. Ans. (a)
3 3 Tc
IAS-9. Ans. (b) According to dimensional homogeneity law unit of molar-volume and ‘b’ must be
same. i.e. m3/mole
IAS-10. Ans. (b)
IAS-11. Ans. (c)
IAS-12. Ans. (d) Van der Waals equation
⎛ a ⎞ RT a
⎜ P + 2 ⎟ (υ − b ) = RT or P = − 2
⎝ υ ⎠ υ −b υ
3 3 Tc
⎛ ∂P ⎞ − RTc 2a
⎜ ⎟ = + 3 =0
⎝ ∂V ⎠T =Tc (Vc − b ) Vc
2
⎛ ∂2 P ⎞ 2.RTc 6a
⎜ 2⎟ = − 4 =0
⎝ ∂V ⎠T =Tc (Vc − b ) Vc
3
⎛ ∂3 P ⎞ 6 RTc 24a
And ⎜ 3⎟ =− − 5 = −9 pc i.e.-ive
⎝ ∂V ⎠T =T
c
( vc − b ) vc
IAS-13. Ans. (a) In adiabatic mixing there is always
increase in entropy so large amount of
irreversibility is these.