AEPaperII PDF

126 Automobile Engineering Technician
UNIT 1
Fundamentals of
Thermodynamics
Learning Objectives
After studying this unit, the student will be able to
• Know about the relation between heat and mechanical energies
• Limitations of heat energy produced
• Heating efects on a perfect gas
1.0 Introduction
The Science which deals with conversion of heat energy into mechanical
energy and the properties of the system is called “THERMODYNAMICS”
This conversion is based on certain laws, generally known as “Laws of
Thermodynamics”.
1.1 Thermodynamic System
The region in the space that contained matter whose behavior is to be
investigated is called “Thermodynamic System” or simply referred as “System”
The System is enclosed by a “boundary” Every thing which is not in the
System i.e. outside the boundary is called “Surrounding”.
Paper - II Basic Mechanical and Electrical Engineering 127
Working Fluid: It is a fluid on which the Thermodynamic processes are

performed. The gases, vapours (steam) and liquids are employed as working
fluids.
State of System: The Thermodynamic state of system or a working
substance is defined by particular values of independent properties. It can be
described by its properties such as temperature, pressure, volume, density etc.
1.2 Types of Thermodynamic System
The Thermodynamics Systems may be classified into the following three
types. 1. Closed System 2. Open System 3. Isolated System
1. Closed System: This is a system of fixed mass and Identity whose
boundaries are determined by the space of the matter (working substance)
Occupied in it.
The gas in the cylinder is considered as a system. If heat is supplied to the
cylinder from some external source, the temperature of the gas will increase and
the piston will rise. In other words, the heat and work cross the boundary of the
system during the process. But there is no addition or loss of the original mass of
the working substance, which comprises the system is fixed.
Weight
Piston
Gas
Boundary
Fig. 1.1
1.2.1 Types of Thermodynamic Systems

Thermodynamics Systems can be classified as
1. Closed System
2. Open System
3. Isolated System
1. Closed System
In closed system there will be only energy transaction with surroundings.
Thus a closed system contains a fixed quantity of matter and has no mass transfer
across its boundary. Only energy may flow across the boundary. ex: The gas
contained in a cylinder.
2. Open System
This system permits the transfer of matter and energy across the boundary.
The mass confined within the boundary may change or it may constant.
Ex: i) Flow of air through the compressor.
ii) Flow of steam through the nozzle and Turbine blades.
3. Isolated System
It has no transaction with surroundings. It will not permit transfer of both
matter and energy across the boundary Ex: Thermodynamic Universe.
1.3 Thermodynamic Properties
A Thermodynamics Property can be defined as any observable character
stick of system.
These are divided into two classes.
1. Extensive properties
2. Intensive properties
An extensive property is one that depends on the mass (Quantity) of the
system.
Ex:- Mass, volume, internal energy, enthalpy etc.
An intensive property is independent of the mass of the system.
Ex:- Specific volume, pressure, temperature, density etc.
For clear understanding the concept, consider an amount of matter that is
uniform in temperature and imagine that it is divided into two parts. The mass of
the whole is the sum of the mass of the two parts; overall volume is the sum of
the volumes of the both parts. However the temperature of the whole is not the
sum of the temperature of the parts.
Here the Mass and volume are extensive properties and the Temperature
is the intensive property.
1.4 Definitions of Some of the Properties

1.4.1 Pressure
The term “Pressure” may be defined as the force per unit area. The Unit of
pressure depends upon the Units of force and area.
In M.K.S System, the practical unit of pressure is Kg/cm2
Sometimes pressure is also mentioned in terms of technical Atmosphere
and is denoted by ata. 1ata= 1kg/cm2
In S.I System, the practical unit of pressure is N/mm2, N/m2, KN/m2 etc
1 pascal = 1N/m2
1 bar = 10.5 N/m2 = 102 K N/m2
1.4.2 Atmospheric Pressure
The Normal force exerted by the atmoshpere on a Unit surface area is
called Atmosphere Pressure” It is measured by mercury barometer
1 atm = 760mm Hg = 1.01325 bar
= 101.325 KN/m2
1.4.3 Gauge Pressure
The Pressure recorded by the instrument above atmospheric pressure is
called “Gauge pressure”
1.4.4 Absolute Pressure
The pressure measured above Absolute Zero pressure is called Absolute
pressure
Absolute pressure = Atmosphere pressure + gauge pressure
= Atmosphere pressure – vaccum
1.4.5 Volume : Volume of a substance is defined as the space which it occupies
and is dependent on the mass of the surface.
It’s basic unit is cubic meters.(m3)
It is also expressed in Liters 103L=1 m3
1.4.6 Specific Volume : The Volume per unit mass of the substance is called
specific volume.
Specific volume, v = V/m m3/kg

1.4.7 Temperature : It is defined as the degree of hotness or level of heat
intensity of a body. It is measured by thermometer in the following commonly
used scales.
(i) Centigrade scale or Celsius scale
(ii) Fahrenheit scale
i) Centigrade Scale or Celsius Scale: This scale is most commonly
used by Engineers and scientists. The freezing point of water in this scale is
“Zero” degree Celsius.
The Boiling point of water is 100oc. (1 each division in this scale is “one”
degree centigrade (It is written as oc)
ii) Fahrenheit scale: In this scale, the freezing point of water is marked
as 32 and boiling point of water as 212. The space between these two points
are divided into 120 equal division and each degree represents 1 degree
Fahrenheit (written as oF)
(c/100) = (F-32)/180
1.4.8 Absolute Temperature
At lowest temperature the gas will occupy zero volume. This lowest
temperature at which the volume of gas is “zero” is called “Absolute Temperature”
It is equal to “-273oc” or “- 460o F” The temperature measured from this zero
is called Absolute temperature.
oK = oc + 273 (K = Kelvin unit)
oR = oF + 460 (R = Rankine unit)
1.4.9 Internal Energy

It is defined as the energy stored or possessed by the thermodynamic
system. The molecules of a gas (real or ideal gas) may be imagined to be in
motion thereby possess kinetic energy of transition, rotation as well as vibration
motion.
For an ideal gas, internal optional energy is ‘zero’ because no inter molecular
force exist between the molecular.
The total change of internal energy is U2 - U1= m. CV (T2-T1)
where m = mass of the gas
Cv= Specific heat at constant volume

T2 = Final temperature
T1 = Initial temperature
Units: In S.I. System the change of Internal energy is expressed in Joules or
kilojoules (J/kg or KJ/ kg)
1.4.10 Enthalpy
It is a derived thermodynamic quantity and is defined as the sum of internal
energy and the product of pressure and volume.
H = U+ pV Joules or Kilojoules
It depends on temperature only energy change in internal energy.
H2-H1 = m.Cp (T2-T1) KJ
1.5 Definitions of Flow of Work and Specific Heat
1.51 Flow of Work
The work done in moving the fluid into or out of the system is called flow of
work.
Consider the fluid crossing the boundary. The approaching fluid must displace
an equal amount of fluid inside the system in order to cross the boundary and
enter the system. The energy required to achieve this is called flow of work.
Area
Fig. 1.2
Flow of work = Force x displacement

= P.A x dx
1.5.2 Specific Heat

Specific heat may be defined as the Quantity of heat required to raise the
temperature of one kilogram of substance through one degree Celsius.
1.5.2.1. Specific heat at constant volume : The specific heat of a gas at
constant volume is defined as the heat required to raise the temperature of 1kg
of gas , by one degree Celsius, heat being supplied at constant volume.
1.5.2.2. Specific heat at constant pressure: The Specific heat of a gas
at constant pressure is defined as the heat required to raise the temperature of 1
kg of gas, by one degree Celsius, heat being supplied at constant pressure.
Summary
1. System : The thermodynamic system is a definite Area or space where
the thermodynamic process is taking place. A thermodynamic system has its
‘boundaries’ and anything outside the boundaries is called ‘Surroundings’.
2. Types of Thermodynamic Systems
a) Closed system
b) Open system
c) Isolated system
Closed System : The system of fixed mass and identify whose boundaries
are determined by the working substance in it.
Open System : In this system, the working substance crosses boundary
of the system. Heat and work may also cross the boundary.
Isolated System : System of fixed mass and no heat or work cross the
boundary.
3. Properties
a) Intensive properties: These properties are independent of the mass of
the system.
Ex.: Specific Volume; pressure, temperature, density etc.,
b) Extensive properties : These properties depends upon the mass of the
system.
Ex.: Mass, Volume, Internal energy, Enthalpy etc.,
4. Pressure
Pressure is a force applied per Unit area and is measured in Units of N/
m2 or Pascal,
5. Volume
Volume of a substance is defined as the space which it occupies and is dependent
on the mass of the substance it’s basic unit is m3.
6. Temperature
It is an indication of degree of hotness or cold ness. It is the measure of
Intensity of heat in metric system, the temperature is Commonly measured in
degree Celsius.
7. Internal Energy
It is the energy stored or possessed by the system. It is independent of
pressure and Volume and is only a function of temperature.
DU = m.cv. d T.
8. Enthalpy
It is the sum of Internal energy and the product of pressure and volume
expressed in consistent units. It is designated in ‘H’
H = U + PV
9. Specific Heat
The amount of heat required to raise the temperature of a unit mass of any
substance through 10C. It is generally denoted by ‘C’
Short Answer Type Questions
1. Define System.
2. Mention the types of thermodynamic systems.
3. Define Intensive properties and give examples.
4. Define Pressure and write its units.
5. What is Internal Energy.
6. Define Enthalpy.
Long Answer Type Questions
1. Mention the types of Thermodynamic system and explain them

2. Define system, Boundary, Surrounding and explain them
3. What is Specific heat? Maintain and explain the types of Specific heats.
UNIT 2
Laws of Perfect Gases
Learning Objectives
• Understand the gas laws like Charle’s, Boyle’s, Avagadro’s etc.
• Relation between Pressure, volume and temperatures of gas.
2.0 Introduction
A Perfect gas (or an Ideal gas) may be defined as a state of a substance
whose evaporation from its liquid state is complete. From this point of view the
substances like oxygen, Nitrogen, Hydrogen and air, within certain temperature
limits, are also regarded as perfect gases.
2.1 Laws of Perfect Gases
The physical properties of perfect gases are controlled by the following
three variables.
1. Pressure exerted by the gas.
2. Volume occupied by the gas.
3. Temperature of the gas.
The behaviour of a perfect gas, undergoing any change in the above
mentioned variables, is governed by certain laws of gases.
2.1.1 Boyle’s Law

This law was formulated by Robert Boyle in the year 1662. It states that
“The absolute pressure of a given mass of a perfect gas varies inversely as its
volume, when the temperature remains constant”.
P  1 / V or PV = constant
The more useful form of the above equation is
P1V1 = P2V2 = P3V3 = ……… = Constant
Mathematically,
P 1/ V or PV = Constant, if temperature remains constant.
If the gas changes from sate (1) to sate (2) at constant temperature, the
two end states are related by the equation :
P1V1 = P2V2
If the change in pressure and volume is represented on P-V diagram,
the path or curve obtained is a rectangular hyperbola, having the equation
PV = constant.
1
P1
PV = C
P2 2
V1 V2 V
Fig. 2.1
2.1.2 Charle’s Law

This Law was formulated by a French scientist Jacques A.C. Charles in
about 1787. it may be stated as
“The volume of a given mass of a perfect gas varies directly as its absolute
temperature, when the absolute pressure remains constant.”
Mathematically,
V  T or V/T = Constant.
(or) V1 =
V2 =
V3 = Constant
T1 T2 T3
The Charles’s law can also be stated as follows :
“ If the volume of a gas is kept constant, then the absolute pressure is
directly proportional to the absolute temperature.”
At constant volume, PT or P/T = Constant
At constant volume P1 = P2
T 1 T2
The change of states at constant pressure and constant volume are
represented on P-V diagrams.
P
1 2
P 1 =P 2 P2 2
P1 1
V V1 =V2
(a) Constant pressure (b) Constant Volume.

Fig. 2.2
2.1.3 Avogadro’s Law

It states, “Equal volumes of all gases at the same temperature and pressure,
contain equal number of molecules.
Thus according to Avogadro’s law.
1m3 of Oxygen (O2) will contain the same number of molecules as 1m3 of
Hydrogen (H2) when the Temperature and pressure remain same.
2.1.4 Joule’s Law
It states, “The change of Internal energy of a perfect gas is directly
proportional to the change of temperature.”
Mathematically dE dT = m.c. dT

where m = mass of the gas nd
c = A constant of proportionality known as specific heat.
2.1.5 Regnault’s Law
It states that “The Specific heats of a perfect gas remain constant when
pressure and volume are constant”.
Thus two specific heats CP and CV of a perfect gas do not change with the
change in temperature.
2.2.1 General Gas Equation
In gas Laws we will get the relation between the two Variables when the
third Variable is constant. But in actual practice, all the three Variables i.e pressure,
volume and temperature change simultaneously. In order to deal with all practical
cases, the Boyle’s Law and Charles’ Law are combined together, which gives
us General Gas equation
According to Boyle’s Law,
P 1 (keeping T constant)
V
V 1
P
According to Charles’ Law
V T (Keeping P Constant)
It is thus obvious that
V 1/P and T
Or V  T
P
 PV T or PV = CT or PV / T = C
Where ‘C’ is a constant whose value depends upon the mass and properties
of the gas constant
i.e. P1V1 P2V2 P3 V3
= = = .................Constant
T1 T2 T3
2.2.2 Characteristic Gas Equation

It is a modified form of general gas equation. If the volume (V) in the gas
equation is taken as that of 1kg of gas (known as specific volume and donated
by VS) then the constant ‘c’ (in the general gas equation) is represented by
constant R (In the characteristic gas equation)
Then PVs = RT
Where R is known as characteristic gas constant for any mass’m kg’ of a
gas ,characteristic gas equation becomes.
m.PVs = m.RT
or PV = m RT ( m Vs =V)
2.2.3 Universal Gas Constant or Molor Constant
The Universal Gas constant or Molar constant (General denoted by Ru) of
a gas is the product of gas constant and molecular weight of the gas.
Mathematically, Ru= MR
Where M = Molecular weight of the gas expressed either in gm (gram
mole) or in kg m. (kg mole) R= Gas constant.
In general if M1, M2, M3 etc are the molecular weight of different gases and
R1,R2, R3 etc are their gas constants respectively….
Then
M1R1 = M2R2 = M3R3 =…………..RU
PV = n RuT
Or RU = PV/nt J/k mole K. or K J / k mole K.
2.3 Specific Heats of Gas
The specific heat of a substance may be broadly defined as the amount of
heat required to raise the temperature of its unit mass through 1oC. All the liquids
and solids have one specific heat only. But a gas can have different specific
heats depending upon the conditions under which it is heated. The following two
are different specific heats.
i) Specific heat at constant volume
ii) Specific heat at constant pressure.
2.3.1 Specific Heat at Constant Volume

It is the amount of heat required to raise the temperature of a unit mass of
agas through 1oC when it is heated at a constant volume.
It is generally dented by CV or KV
Consider a gas contained in a Container with a fixed lid.
Now if this gas is heated, it will increase the temperature and pressure of
the gas in the container.
Since the lid of the container is fixed, the volume of gas remains unchanged.
Fixed Lid
Fig. 2.3
M = Mass of the gas

T1 = Initial Temperature of the gas
T2 = Final Temperature of the gas
 Total heat supplied to the gas at constant volume

= H = Mass x sp. Heat at constant volume x Rise in temperature .
= M. Cv (T2 – T1)
Whenever a gas is heated at constant volume, work is done by the gas.
The whole heat energy is utilized in increasing temperature and pressure of
the gas.
That means - all the amount of heat supplied remains within the body of the
gas, and represents the increase in internal energy of the gas.
2.3.2 Specific Heat At Constant Pressure

It is the amount of heat required to raise the temperature of a unit mass of
gas through 10C, when it is heated at constant pressure.
It is generally denoted by CP or KP
Consider a gas contained in a container with a movable lid. If the gas heated,
it will increase the temperature and pressure of the gas in the container.
Since the lid of the container is movable, it will move upwards, in order to
counter balance the tendency for pressure to raise.
Movable lid
Fig. 2.4
Let m = mass of the gas

T1 = Initial temperature of the gas
V1 = Initial volume of the gas
T2, V2 = Corresponding values for final conditions of the gas.
 Total heat supplied to the gas, at constant pressure,

H = Mass x Sp. Heat at constant
Pressure x Rise in temperature.
= M. CP (T2 – T1)
2.3.3 Relation Between Two Specific Heats
Consider a gas enclosed in a container and being heated at constant pressure.
Let M = Mass of the gas
T1 = Initial Absolute temperature or the gas

T2 = Final Absolute temperature of the gas
V1 = Initial volume of the gas
V2 = Final volume of the gas
CP = Specific heat at constant pressure
CV = Specific heat at constant volume
P = Constant pressure
As we know that,
The heat supplied to the gas at constant pressure,
H = M.CP (T2 – T1)
As already discussed, a part of this heat is utilized in doing external work,
and the rest remains within the gas, and is used in increasing the internal energy
of the gas.
Heat utilized for external work,
W= P (V2 - V1)
………………………… ........(i)
J
And increase in internal energy ,
E = m.CV (T2 - T1) ......……………………………(ii)
We know that H = W+E ...………………………….(iii)
 M. CP (T2-T1) = P(V2-V1) + M.CV (T2 - T1) ………(iv)

J
Using characteristic gas equation, (ie. PV = m RT)
We have
PV1 = m RT1 (for initial conditions)
P V2 = m RT2 (for final conditions)
P (V2-V1) = mR (T2 - T1)
Now substituting the value of P (V2-V1) in equation (v)
M CP (T2-T1) = m.R (T2-T1)

+ m CV (T2 - T1)
J
 CP = R / J + Cv ....……………………. (vi)
(or) CP – CV = R / J ….......……………………. (vii)
The above equation may be re-written as
CP – CV = R / J
CV ( -1) = R / J (Where  = cp / cv)
Cv = R / J(-1)
Where R is a gas constant and its volume is taken as
0.287 KJ / Kg Ok
The characteristic gas constant of a gas is equal to the difference of its two
specific heats.
Now Consider a certain quantity a perfect gas being expanded adiabatically.
Let V1 = Initial volume of the gas
P1= Initial pressure of the gas
V2= Final volume of the gas
P2= Final pressure of the gas
Now consider at any Point ‘E’ on the curve AB. Let ‘P’ and ‘V’ be the
volume of the gas at this point ‘E’
Let the volume of gas increase by a small amount dv.
This change is so small that the pressure during the change may be assured
to remain constant.
: Work done during this change,
Dw = P.dv …. (In work Units)
= P.dv/J….. (In heat Units)
As the work done is at the expense of Internal energy, the internal energy
must decrease by an equal amount
Let the temperature of the gas fall by a small amount ‘dT’
Then decrease internal energy = dE= mcv dT

Since dE+ dw=0
: mcv dT+ pdv/J=0
Or mcvdT = -pdv/J….(i)
We know that pv= mRT
Differentating this expression, we get
Pdv+vdp = mRdT…..(ii)
We also know that R=J(Cp-Cv)
Substiting value of R in equation (ii)
Pdv + vdp = mJ(cp-cv)dT
Mj(cp-cv) dT = pdv + vdp….(iii)
Dividing Equation III by Equation(i)
mJ(cp-cv) dT/mcvdT= pdv +vdp/-pdv/J
cp-cv/cv = -1-(v/dv x dp/p)
cp/cv -1-(v/dv x dp/p)
V = -(v/dv x dp/p)
(: cp/cv =r)
:V x dv/v = -dp/p
V dv/v + dp/p =0
Integrating both sides.
Vlog e v + log e p = constant
Or log PV2 = log e c
PV2 =c
Or P1V1 = P2 V2 =…….C…..(iv)
Or P1/P2 = (V2/V1)…….(v)
Summary
1. The physical properties of perfect gases are controlled by
(i) Pressure exerted by the gas

(ii) Volume occupied by the gas
(iii) Temperature of the gas
2. Boyle’s Law : The absolute pressure of a given mass of the perfect
gas varies inversly as its volume, when the temperature remains constant.
P 1/ v or PV = Constant
3. Charle’s Law : The volume of a given mass of a perfect gas varies di-
rectly as its absolute temperature, when the absolute pressure remains constant.
V or V /T = constant
4. Avagadro’s Law : Equal volumes of all gases at the same temperature
and pressure, contain equal number of molecules.
5. Joule’s Law : The change of Internal energy of a perfect gas is directly
proportional to the change of temperature.
dE dT = m.c.dT
6. Regnault’s Law : The specific heats of a perfect gas remain constant
when pressure and volume are constant.
7. General Gas Equation :
P1V1 P2V2 P3V3
= = = ............... Constant
T1 T2 T3
8. Characteristic Gas Equation
PV = mRT
9. Universal Gas Constant (or ) Molar Constant
The universal gas constant or Molar constant of a gas is the product of the
gas constant and molecular weight of the gas.
Ru = MR
10. Specific heat of a gas at constant volume : It is the amount of heat
required to raise the temperature of a unit mass of gas through 1oC, when it is
heated at constant volume
11. Specific heat of a gas at constant pressure : It is the amount of heat
required to raise the temperature of a unit mass of gas through 1oC, when it is
heated at constant pressure.

1. State Boyle’s Law
2. State Charle’s Law
3. Mention Avagadro’s Law
4. State Joule’s Law
5. State Regnault’s law
6. What is universal gas constant
7. Define specific heat of a gas at constant volume
8. Define specific heat of a gas at constant pressure.
1. Explain Charle’s law with the help of P-V diagram
2. Explain Boyle’s law with the help of P-V diagram.
3. Derive general gas equation.
UNIT 3
Laws of Thermodynamics
Learning Objectives
• Understand on which laws of thermodynamics, the thermodynamic
process will work
• To know about the operations of IC Engines and other related any kind
of heat engines and their performances.
3.1 Laws of Thermodynamic
The amount of useful work and power which can be developed by the
engine, and the possible efficiency of the engine are governed by the laws of
Thermodynamics.
3.1.1 Zeroth Law of Thermodynamic
It states that ‘when two bodies are in thermal equilibrium with a third body,
they are also in thermal equilibrium with each other and hence they are at the
same temperature.
If the bodies A and B are in thermal equilibrium with body C, then A and B
must be in thermal equilibrium.
Thermal Equilimbrium
Th
m u
erm
bri
al
ilim
E
qu
qu
ilim
al E
br
erm
ium
Fig. 3.1
Th
Fig. 3.1 Zeroth Law of Thermodynamics
3.1.2 First Law of Thermodynamic

It states that ‘the heat and mechanical work are mutually convertible.’
According to this law, a definite amount of mechanical work in needed to produce
a definite amount of heat and vice versa.
The First Law of Thermodynamics can also be stated as, “the energy can
neither be created nor destroyed, though it can be transformed from one form
to another”.
According to this law, the energy due to heat supplied must be balanced by
the external work done plus gain in internal energy due to rise in temperature.
Mathematically H= E + W.
Where H = Heat transferred.
E = Change in internal energy
W = Work done in heat units.
dH = dE + dW.
3.1.3 Second Law of Thermodynamics
It states that ‘There is a definite limit to the amount of mechanical energy,
which can be obtained from a given quantity of heat energy’.
According to Claussius, ‘It is impossible for a self acting machine working
in a cyclic process, to transfer heat from a body at a lower temperature to a
body at a higher temperature without the aid of a external agency.
According to Kelvin - Plank, ‘It is impossible to construct an engine working

in a cycle, that will produce no other effect than the extraction of heat from a
single heat reservior and the performance of an equal amount of work.
Summary
Zeroth law of thermodynamics : When two bodies are in thermal equilimbrium
with a third body, they are also in thermal equilimbrium with each other and
hence they are at the same temperature.
First Law of Thermodynamics : The energy can neither be created nor
destroyed though it can be transformed from one form to another.
Second Law of Thermodynamics : There is a definite limit of amount of
mechanical energy which can be obtained from a given quantity of heat energy.
1. State Zeroth law of Thermodynamics.
2. State First law of Thermodynamics
3. State Second law of Thermodynamics.
1. Explain the laws of Thermodynamics.
UNIT 4
Thermodynamic Processes
Learning Objectives
After studying this unit, the student will be to
• Know the different processes applied on gases like constant volume,
constant pressure, constant temperature etc.
• The relation between the specific heats of constant volume and constant
pressure processes.
• Know about work done during different processes and the heat energy
developed through them
4.0 Introduction
The process of heating and expanding of a gas may, broadly, be defined as
a thermodynamics process or non flow process.
It has been observed that as a result of flow of energy, change takes place
in various properties of the gas such as pressure, volume, temperature, specific
energy, specific enthalpy etc.
Some of the important thermodynamics processes are
1. Constant volume process
2. Constant pressure process

3. Hyperbolic process
4. Isothermal process (constant temperature process).
5. Adiabatic process (or) Isentropic process.
6. Polytrophic process.
7. Free expansion process.
8. Throttling process.
4.1.1. Constant Volume Process
As we already know that when a gas is heated at constant volume, its
temperature and pressure will increase. Since there is no change in its volume,
no external work is done by the gas. All the heat supplied is stored in the body
of the gas in the form of internal energy.
Now consider m kg of a certain gas being heated at constant volume from
an initial temperature T1 to final temperature T2.
2
P2
P1 1
Volume
Fig. 4.1 P-V diagram
We know that H = E + W
Or H = E (since W = 0)
We also know that
Internal Energy, E = mCV (T2 – T1)
Heat supplied, H = 3 = m. mCV (T2 – T1).
4.1.2 Constant Pressure Process

When a gas is heated at a constant pressure, its temperature and volume
will increase. Since there is a change in its volume, the heat supplied is utilised in
increasing the internal energy of the gas an also for doing some external work.
Now consider m kg at a certain gas being heated at a constant pressure
from an initial temperature T1 to the final temperature T2.
1 2
P
Pressure
V1 V1
Volume
Fig. 4.2
We know that the heat supplied to the gas at constant pressure, H = mCV
(T2 – T1) increase in internal energy, E = mCV (T2 – T1) and work done during
the process.
W = Area below the line 1-2.
4.1.3 Constant Temperature Process (Isothermal Process)
A process, in which the temperature of working substance remains constant
during its expansion or compression, is called an ‘Isothermal process’ or constant
temperature process.
This will happen when the working substance remains in a perfect thermal
contact with the surroundings.
As there is no change in temperature, there is also no change in internal
energy.
H=E+W
Therefore H = O + W …………………………………( E = 0)
Or H = W ………………….....................……. (In work units).
or H = W/J ……………….. ( in heat units).
Hence, during Isothermal expansion of a gas, Heat added = Work done by

the gas.
Similarly, during isothermal compression of a gas,
Heat substracted = Work done on the gas.
Isothermal process is governed by Boyle’s law,
 Perfect gas pv = constant work done during isothermal expansion.
A
P1
Pressure
P E
P2 B
dV
V1 V2
Volume
Fig. 4.3
Let V1 = Initial volume of gas

P1 = Initial pressure of gas
V2 = Final volume of gas
P2 = Final pressure of gas.
Now consider any point E on the curve AB.
Let P and V are pressure and volume of gas at the point E.
Let Volume of the gas increase by a very small amount dv.
This change is so small that the pressure during the change may be
assumed to remain constant.
dw = area of the shaded portion = P.dv.
Now, the total work done during expansion from A to B is can be obtained
by integrating the above equation between the limits V1 and V2.
Therefore the work done, W = Area under the curve AB
=  p.dv .............. (i)

V
Since the expansion is Isothermal, i.e.2 pv = c
Therefore PV = P1V1 V1
Therefore P = P1V1/V.
Substituting the value of P in equation (i)
V2 V2 dv
w = P1V1
dv = P1V1 
V1 V
V V1
V2
= P1V1 log e V = P1V1 loge V2 / V1
V1
Using logarithem table

w = 2.3 P1V1 log V2 / V1
(0r) 2.3 P1V1 log r. (r = expansion ratio)
we know that P1V1 = mRT
 Work done = w = 2.3 mRT log V2 / V1
= 2.3 m RT log r
Sine P1V1 = P2V2 , then V2 / V1 = P1 / P2
 Work done = w = 2.3 P1V1 log P1 / P2
4.1.4 Adiabatic Process (or) Isentropic Process
A process in which the working substance neither receives nor gives out
heat to its surroundings, during its expansion or compression is called ‘Adiabatic
Process’.
This will happen when the working substance remains thermally insulated,
so that no heat enters or leaves it during the process.
Thus in an adiabatic process,
1. No heat enter or leaves the gas.

2. As the temperature of gas changes, the work is done at the expense of
internal energy.
3. The change in internal energy is equal to the mechanical work done.
We know that H=E+W
O = E + W………………………. ( H = 0)
 E = - W……………………….. (in work units).
Minus sign indicates that, for increase in internal energy work must be done
on the gas.
i.e. Negative work must be done by the gas.
Similarly, for decrease in internal energy, work must be done by the gas.
Now consider a certain quantity a perfect gas being expanded adiabatically.
A
P1
Pressure
P E
P2 B
dV
V1 V2
Volume
Fig. 4.4
Let V1 = Initial volume of gas

P1 = Initial pressure of gas
V2 = Final volume of gas
P2 = Final pressure of gas.
Now consider any point E on the curve AB.
Let P and V are pressure and volume of gas at the point E.
Let the volume of the gas increase by a very small amount dv.
This change is so small that the pressure during the change may be assumed
to remain constant.
 Work done during this change,
dw= p.dv ………………………………….(in work units)
= p.dv/J ………………………….…….(in work units).
As the work done is at the expense of internal energy, the internal energy
must decrease by an equal amount. Let the temperature of the gas fall by a small
amount ‘dT’, then decrease in internal energy = dE = mCV dT.
Since dE + dw = 0.
Therefore mCV dT + p dv/J = 0
Or mCV dT = - p dv/J ……………………….(i)
We know that pv = mRT.
Differentiating this expression, we get
pdv + v.dp = m R dt ……………(ii)
we also know that R = J(CP – CV)
substituting value of R in equation (ii)
pdv + v dp = mJ ((CP – CV)dT.
mJ(CP – CV)dT = pdv + Vdp ………..(iii)
dividing the equation (iii) by equation (i)
Pdv+ vdp
mJ (Cp - Cv) dT pdv
=
m Cv dT - pdv
J
(Cp - Cv) v dp
= -1- x p
Cv dv
v dp
 = - x p
dv
 dv = -dp
v p
 dv both dp
Integrating + sides
v p =0
v
loge + loge P = constant
or loge Pvr = loge C
or Pvr = c
or P1V1r = P2V2r = ............ C
dividing equation III by equation (i)
mJ (Cp - Cv) dT PdV + vdp
mCvdT -pdv
= J
Cp - Cv v dp
Cv dv P
= -1- x
Cp v dp
Cv dv P
-1- = -1- x
 = - v dp
dv P  Cp / Cv = 
 x dv / V = -dp / p
x dv / V = -dp / p = 0
Integrating both sides
 loge V + logeP = constant
or loge PVr = log eC
Pvr = C
or P1V1r = P2V2r = ..................... = C .........(iv)
or P1 / P2 = (V2 / V1) r ............................... (v)
from general gas equation, we know that

P1V1 P2V2
=
T1 T2
P1 T1 V2
= x ............................ (vi)
P2 T2 V1
Equation (v) and (vi)

P1 V2
=
P2 V1

T1 V2 V2
x =
T2 V1 V1

V2
T1 
V1 V2
= =
T2 V2 V1
V1
From general gas equation P1 V1 / T1 = P2V2 / T2

P1 T2 V2
x =
T1 V1P2
  
P1 P1 T 2 P1 T2
= x = x
P2 P2 T 1 P2 T1
P1

P2 
T2 P1
= =
T1  P2
P1
P2
 
T2 P2
=
T1 P1

T2 P2
=
T1 P1
Work done by the Gas :

For any non flow process
V2
Wordone, W1-2 =
P dV
V1
But we know that the process follows

PV = C
P = C / V
V2
V2
C
W1-2 =  
dV = C  V- dV
V1 V V1
V2
V - V2 -  V1-
=C =C
-  - 
V1
C.V2 -  C.V1-

=
- 
P2 V2 V2-  P1 V1 . V1

=
- 
P2 V2 P1 V1
=
- 
P1 V1 P2 V2
Workdone , W1-2 =

mR (T1-T2)

4.1.5 Polytropic Process

The polytropic process is also known as the general law for the expansion
and compression of gases and is given by the relation
Pvn = Constant
Where ‘n; is a polytropic index which may have any value from ‘zero’ to
‘Infinity’ depending upon the manner in which expansion or compression has
taken place.
The various equations for polytropic process may be expressed by changing
the index n for r in adiabatic process.
n-1 (n-1)/n
T1 V2 T1 P1
= and =
T2 V1 T2 P2
Similarly V1 / V2 = ( P2 / P1)1/n
Work done by the gas for any non flow process
V2
Work done = W1-2 =  Pdv
V1
As per polytropic law PVn = C Since P = C / Vn
V2
C
W 1-2 =
 dV
V1 V
V2
V2 -n+1
V
=C  Vn dv = C
V1 -n +1
V1
1
P1
P PVn = C
P2 2
V1 V2 V
V2 -n+1 - V1 -n+1 C V2 -n+1 - CV1 -n+1

=C =
-n +1 -n +1
But P1 V1 n = P2 V2 n = C
P2 V2 n V2 -n+1 - P1 V1 n V1 -n+1 P2 V2 - P1 V1
= =
-n +1 -n +1
P1V1 - P2 V2 mR (T1-T2)
Therefore W1-2 = or
n-1 n-1
(Since Pv = mRT)
Summary
1. Constant volume process : When a gas is heated at constant volume,
its temperature and pressure will increase. All the heat supplied is stored in the
body of the gas in the form of internal energy.
2. Constat Pressure Process : When a gas is heated at constant pressure,
its temperatuer and volume will increase. Since there is a change in its volume,
the heat supplied is utilized in increassing the internal energy of the gas.
3. Isothermal Process : A process in which the temperatuer of working

susbtance remains constant during its expansion or compression is called
Isothermal process.
4. Adiabatic Process : A process in which the working substance neither
receives not gives out heat to its surroundings, during its expansion or compression
is called Adiabatic Process.
1. Define Constant Volume proess
2. Define Constant pressure process.
3. Define Isothermal process.
4. Define Adiabatic process
1. Explain constant volume process with P-V diagram and write the formulae
for work done.
2. Explain the constant pressure process with P-V diagram and write the
formulae for work done.
3. Explain the constant temperature process with P-V diagram and write
the formula for work done.
4. Explain the Adiabatic process with P-V diagram.
UNIT 5
Fuels
Learning Objectives
After studying this unit , the student will be able to
• Understand the term fuel
• Different types of fuels with examples, comparision of solid, liquid and
gaseous fuels.
• Qualities of good fuel.
• To know about octane number, cetane number.
• To know about alternate fuels.
5.0 Introduction
A fuel may be defined as a substance, which on burning with oxygen in the
atmosphere air, produces a large amount of heat. The amount of heat generated
is known as Calorific value of the fuel.
As the main constituents of fuel are carbon and hydrogen, these are also
known hydrocarbon fuels.
5.1 Types of Fuels
The fuels maybe classified into three general forms:
1. Solid fuels 2. Liquid fuels 3. Gaseous fuels
Each of these fuels may be further subdivided into following two types.
(a) Natural fuels and (b) Prepared fuels.
5.2.1 Solid Fuels
The natural solid fuels are ‘wood’, ‘peat’, ‘lignite’ or ‘brown coal’,
‘bituminous coal’ and ‘anthracite coal’.
The prepared solid fuels are wood charcoal, cake, briquetted coal and
pulverized coal.
5.2.1 (a) Wood
In rural areas and also in olden days, it was extensively used as a fuel for
cooking purpose. It consists of mainly carbon and hydrogen. The wood is
converted into coal when burnt in the absence of air. The calorific value of wood
varies with its kind and moisture content. The average calorific value of the
wood is 4,700 k. Cal/kg.
5.2.1. (b) Peat
Peat is the first stage in the formation of coal from wood. It is a spongy
humified substance found in boggy land. It has a large amount of water contents
upto 30% and therefore has to be dried for a longer period before using it as a
fuel. It’s calorific value is 5500 k.Cal/kg.
5.2.1 (c) Lingnite (or ) Brown Coal
It is the next stage of peat in the formation of coal. It is the between
stage of ‘peat’ and ‘bituminous coal’. It contains nearly 40% of moisture and
60% of carbon. It is brown in colour and it is also known as ‘brown coat’.
These are used in generation of thermal power, Fertiliser manufacturing. It’s
average calorific value is 6000 k.Cal/kg.
5.2.1 (d) Bituminous Coal
It is the next stage of lignite in the coat formation. It contain very little
moisture of about 4 to 6% and carbon content is high as much as 75% to 90%.
It’s average calorific value is 8000 k.Cal/kg.
It is of two types.
(i) Coking Bituminous coal: It is also known as soft coal. It is soft in
condition and swells on heating. It is mainly used in manufacturing of gas.
(ii)Non-coking Bituminous coal: It gives little or no-smoke. It is mostly
used as fuel for stream boiler. Hence it is also known as steam coal.
5.2.1 (e) Anthracite Coal

It is the final stage of coal formation. It contains 90% or more carbon with
a very little volatile matter. It is comparatively smokeless and has very little
flame. It possesses a high calorific value of about 8600 k.Cal/kg and is used for
steam raising and general power purposes.
5.2.1 (f) Wood Charcoal
It is made by heating wood with a limited supply of air to a temperature of
not less than 280°C. it is a good prepared solid fuel and is used for various
metallurgical purposes.
5.2.1. (g) Coke
It is produced when coal is strongly heated continuously for 42 to 48 hours
in the absence of air in a closed vessel. This process is known as Carbonisation
of coal.
Coke is dull black in colour, porous and smokeless. It has high carbon
content of 85% to 90% and has a higher calorific value than coal.
The soft coke or lower temperature coke is carbonized at a temperature of
500° to 700°C and is used as domestic fuel.
The hard coke or high temperature coke is carbonized at a temperature of
900° to 1100°C and is used in blast furnace for extracting ‘Pig Iron’ from Iron
ore and also used in cupola furnace for producing cast Iron.
5.2.1 (h) Briquetted Coal
It is produced from finely ground coal by moulding under pressure with or
without a binding material.
5.2.1 (i) Pulverised Coal
It is the low grade coal with high ash content, is powdered to produce
pulverized coal. It is widely used in cement industry and also in metallurgical
processes.
5.2.1 (j) Solid Fuels
Solid fuels are having the following advantages
• Cheaper than any other fuel.
• Coal is the raw material for producing other fuels such as coke, producer
gas, water gas etc.
• Risk of fire is minimum.

Limitations
• These fuels contain in combustible matter.
• They need large amount of storage space.
• Properties of these fuels are not uniform.
• Handling is not easy and therefore may be costly sometimes.
5.2.2 Liquid Fuels
Almost all commercial liquid fuels are derived from natural petroleum (or
crude oil). The crude oil is obtained from bored holes in the earth’s crest in
certain parts of the world. The liquid fuels consists of hydro carbons.
The natural petroleum may be separated into petrol or gasoline, paraffin oil
or kerosene, fuel oils and lubricating oils by boiling the crude oil at different
temperatures and subsequent fractional distillation. Some liquid fuels are also
obtained from coal (coal tar etc). The following are the some of the important
liquid fuels:
Petrol or gasoline: Petrol is the highest and most volatile liquid fuel. It is
mostly used as fuel for petrol engines, air craft engines (aviation petrol). It is
distillated at temperature from 65°C to 220°C. It’s calorific value is 11,000
k.Cal/kg and above.
Kerosene or paraffin oil: It is obtained by fractional distillation of crude
oil between 220°C and 345°C. it is used as fuel for some stationary engines etc.
Diesel: It is obtained by straight distillation of several crude oils. It is used
as fuel for diesel engines.
Heavy fuel oil: It is obtained by distillation of crude oil between 200°C to
360°C. These oils are mostly used in steam power plants, heating furnaces and
in diesel engines also. It is distillated at a temperature from 345°C to 470°C.
Merits and Demerite of Liquid fuels over solid fuels:
Following are merits and demerits of liquid fuels over solid fuels.
a) Merits:
i) Higher calorific value.
ii) Lower storage capacity
iii) Better economy in handling
iv) Better content of consumption by using valves.

v) Better cleanliness and freedom from dust.
vi) Practically no ashes
vii) Non-corrosion of boiler plates.
viii) Higher efficiency.
(b) Demerits
i) Higher cost
ii) Greater risk of fire
iii) Costly containers are required for storage and transport.
Gaseous Fuels
The natural gas is usually found in or near the petroleum fuels, under the
earth’s surface. It consists of marsh gas or methane (CH4) together with small
amounts of other gases such as ethane (C2H6), carbon dioxide (CO2) and carbon
monoxide (CO). The common example of manufactured gases are Coal gas,
producer gas, water gas, mond gas, coke over gas and blast furnace gas.
Natural Gas
Natural gas is found in the petroleum fields under the earth’s surface. It
consists of methane (CH4) and ethane (C2H6) together with small amounts of
hydrogen sulphide, carbon dioxide and nitrogen.
Coal Gas
It is obtained by destructive distillation of bituminous coal in a fire clay
retort. It consists of carbon monoxide, carbon dioxide, hydrogen and methane.
It is used in boilers, gas engines, and also for lighting and heating applications.
Producer Gas
It is obtained by partial burning of coke in a mixed air stream blast. It
consists of hydrogen. It is mainly used in power generation and glass melting
furnaces.
Water gas (Blue gas):
It is produced by blowing the steam through red hot coal or coke. It consists
of carbon monoxide and hydrogen along with small amounts of carbon dioxide
and nitrogen.
Mond Gas:
It is produced by passing air and large amount of steam over wate coal at
650°C. It is used in furnaces, gas engines and for heating purposes.
Coke over Gas:
It is a by-product from coke over and is obtained by the carbonization
of bituminous coal. It is used for industrial heating and power generation.
Blast Furnace Gas:
It is a by-product in the production of pig iron in the blast furnace. It is used
as fuel in steel works; for power generation; in gas engines; for stream raising in
boilers and for pre-heating the blast furnace.
Merits and Demerits of Gaseous Fuels:
Merits
1. As the supply of fuel gas can be controlled by operating valves;
temperature of the furnace can be controlled easily and accurately.
2. These gases are directly used in internal combustion engines.
3. They are free from liquid and solid impurities.
4. They do not produce ash or smoke.
5. Minimum air is needed for their complete combustion.
Demerits:
1. They are readily inflammable.
2. They require large storage capacity.
Calorific Value of Fuels
The calorific value or heat value of a solid or liquid fuel may be defined as
the amount of heat given out by the complete combustion of ‘1kg’ of fuel. It is
expressed in terms of k.Cal/kg of fuel. However, the calorific value of gaseous
fuels is expressed in terms of k.Cal/m3 at a specified temperature and pressure.
These are two types of calorific values of fuels:
(i) Gross or Higher calorific value.
(ii) Net of Lower calorific value.
Gross or Higher Calorific Value:

All fuels usually contain some percentage of hydrogen when a given quantity
of fuel is burnt, some heat is produced. Moreover, some hot flue gases are also
produced. The water content of the fuel is converted into steam. If the heat is
recovered from the flue gases and the stream is condensed from the flue gases
and the steam is condensed back to water at room temperature (i.e. 15°C),
then the amount of total heat produced per kg is known as Gross or Higher
Calorific value.
In other words, ‘the amount of heat obtained by the complete combustion
of 1kg of fuel, when the products of the combustion are cooled down to the
temperature of supplied air of 15°C is called Gross or Higher Calorific value of
fuel’.
It is briefly written as H.C.V.
Net or Lower Calorific Value:
When the heat absorbed or carried away by the products of combustion is
not recovered and the steam formed during combustion is not condensed, then
the amount of heat obtained per kg of the fuel is known as Net or Lower Calorific
value of the fuel. It is briefly written as L.C.V.
If the H.C.V. is known, then the L.C.V. may be obtained by subtracting the
amount of heat carried away by the products of combustion from H.C.V.
Therefore L.C.V. = H.C.V. — Heat of steam formed during combustion.
The amount of heat per kg of steam in latent heat of steam is 586 k.cal/kg,
and the amount of steam formed in 9H2.
Therefore L.C.V. = H.C.V. – (9H2 x 586) k.Cal/kg.
In SI units, the corresponding relation is L.C.V. = H.C.V. – (9H2 x 2442)
k.Cal/kg.
Fuels Used in I.C. Engines
The thermally crossed and straight run gasoline and mixed to obtain
commercial motor fuel.
There are following three grades of fuels are available.
The following three grades of fuels are available in market for automotive
use.
a. Super premium grade of fuel
b. Premium grade fuel

c. Regular grade fuel.
The automotive fuels are marked under state and federal specifications.
These specifications cover the major characteristics of gasoline, which are related
to the operation of the engine.
Petroleum consists of many hydrocarbon series such as paraffin series,
olefin series, aromatic series, etc.
Paraffin - CnH2n+2: Methane, ethane, hexane, hexadecane.
Olefin - CnH2n: Ethene, Propene, butane.
Naphthene - CnH2n: Cyclic compounds, saturated.
Aromatic - CnH2n-6: Susceptible to oxidation, highly anti knocking.
Diolefin - CnH2n-2: Extremely active, tends to polymerize.
Cyclic - CnH2n-2:
CnH2n-4 These series predominate in the higher boiling point
oils such as gas oils and lubricating oils.
CnH2n-8:
Other constituents — Sulphur, oxygen compounds, nitrogen arphaltenes
and resins.
Characteristics of Gasoline: Major characteristics of gasoline are as
follows:
1. Volatility 2. Anti knock quality 3. Sulphur content
4. Gum content 5. purity 6. Calorific value
7. Operating economy.
1. Volatility: It is the tendency of gasoline to pass from the liquid into the
vapour state at any give temperature.
2. Anti knock quality: The pressure increases evenly inside the engine
cylinder during the normal combustion of air fuel mixture. But under some
condition, the last part of compressed air fuel mixture explodes which suddenly
increases the pressure. This causes knocking noise that sounds like hammer
blow on the piston heat. Certain chemicals are mixed with gasolines to decrease
the knocking quality of gasoline.
3. Sulphur content : The crude oil consist of sulphur while refining the
crude oi, part of sulphur is carried to the gasoline. Too much sulphur is likely to
corrode cylinder bores, bearing surfaces and exhaust systems. Hence the sulphur
contents are to the removed.
4. Gum Content : A good fuel should have a minimum amount of gum.
When gasoline is exposed to air, some of the hydro carbons are oxidized into
sticky gum which causes sticking of values, clogged carburetor etc. The gumming
tendencies of the gasoline can be controlled by proper chemical treatment by
adding suitable gum inhibitor or anti oxidant.
5. Purity : the gasoline used as motor fuel must be free from dirt, grease
and traces of chemicals and water. These should be removed properly in a
refinery.
6. Calorific Value : The engine fuels must have calorific values upto 24000
CHU/kg.
7. Operating Economy : The nature of the fuel is one of the most important
factors which determines the kilometers per litre of the fuel. It also depends on
conditions of the engine, roads on which vehicle travels etc.
Octane Number
The anti knock value of fuel is measured in octane number rating (ONR).
The fuel is iso-octane resistant to knock. It is given an octane rating of 100.
Iso octane and heptane are the reference fuels to test the ONR of the
unknown fuels. These fuels are mixed in certain proportion to the given fuel to
determine octane rating. There are two basic methods.
1. Laboratory method
2. Road test method.
Diesel Engine Fuel
Diesel is light, with low viscosity and high cetane number rating. Diesel
must have the following requirements to operate satisfactorily.
1. It must ignite readily and burn evenly.
2. It must have certain lubricating qualities as the diesel is being operated
in pumps and nozzles etc.
3. it must have low viscosity so that it can readily be atomized.
4. It should not have large foreign matter deposits which may damage the
engine parts.
Properties of Diesel
The following are the desirable properties for diesel.
i) Grade
ii) Gravity
iii) Pour point
iv) Volatility
v) Flash point
vi) Cetane rating
vii)Distillation recovery
viii) Viscosity
ix) Water and sediment
x) Reduction of ash
xi) Less corrosion
Cetane Rating
The number is an indication of ignition quality and the rapidity with which
the fuel in burned after injection takes place. Usually 45 to 60 cetane is the
range of cetane. Between 50 to 55 is the normal cetane rating.
Alternate Fuels:
Alternate fuels are known as Non-conventional or advanced fuels. These
are the materials which can be used as fuels other than conventional fuels include
petroleum fuels, coal, propane, natural gas etc.
Some well known alternative fuels include Biodiesel, Bioalcohol (methanol,
ethanol, Intanol), chemically stored electricity (batteries, fuel cells), hydrogen,
non-fossil methane non-fossil natural gas, vegetable oils and other biomass
sources.
Biomass
Biomass in the energy production industry is living and recently dead
biological material which can be used as fuel or for industrial production.
Biodiesel
Biodiesel are made from animal fats or vegetable oils, renewable resources
that come from plants such as soya bean, sunflower, corn, olive, peanut, palm,
coconut, cotton seed etc., Biodiesel is prepared from the chemical reaction
while mixing of these fats after filtering their hydro carbons and then combined
with alcohol like methanol. These biodiesel produce small quantity of pollutants.
Alcohol Fuels
Butanol fuels, ethanol fuel and methanol fuel are known as Alcohol Fuels.
Methanol and ethanol fuel are primary sources of energy. These can be used
directly in internal combustion engines as alternative fuels.
Ammonia
Ammonia can be used as fuel. A small machine can be setup to create the
fuel and it is used where it is made.
Hydrogen Fuel: Hydrogen is emissionless fuel. The by-product of hydrogen
burning is water.
HCNG
HCNG (OR H2CNG) is a mixture of compressed natural gas and 4 – 9%
of hydrogen by energy.
Compressed Air:
Some of the engines are using compressed air as fuels.
Alternative Fossil Fuels:
Compressed natural gas (CNG) is a cleaner burning alternative to
conventional petroleum automobile fuels. It’s energy efficiency is generally equal
to that of gasoline engines, but lower compared with modern diesel engines.
Natural gas like hydrogen, is another fuel that burns cleanly. Also none of
the smog-forming contaminates are emitted.
Requirements of Good Fuel
A good guel should have a low ignition point
It should have high calorific value
It should freely burn with high efficiency, once it is ignited
It should not produce harmful gases
It should produce least quality of smoke and gases

It should be economical, easy to store and convenient to transport.
Summary
1. Fuel is a substance mostly contains carbon and hydrogen which on
burning with oxygen in the atmospheric air, produces a large amount of heat.
2. The amount of heat generated is known as calorific value.
3. Types of fuels (i) Solid fuels (ii) Liquid Fuels (iii) Gaseous fuels.
Again these are sub divided as (a) Natural fuels (b) Prepared fuels
4. Types of Solid Fuels : Wood, Peat, Lignite, Bituminous coal, Pulverised
coal.
5. Liquid Fuels : Petrol , Kerosene, Diesel, Heavy fuel oil
6. Gaseous Fuels : Natural gas, coal gas, producer gas, water gas, coke
oven gas etc.
7. Calorific value of fuel : It may be defined as the amount of heat given out
by the complete combustion of ‘1 kg’ of fuel. It is expressed in terms of K.cal /
kg of fuel.
These are two types
(a) Gross or higher calorific value (b) Net or Lower calorific value
1. Define fuel.
2. Mention types of solid fuels
3. Mention types of liquid fuels.
4. Mention types of gaseous fuels
5. Define calorific value.
1. Explain the types of solid fuels
2. Explain the types of liquid fuels
3. Explain the merits and demerits of Liquid fuels over solid fuels.
UNIT 6
Thermodynamic Cycles
Learning Objectives
• Understand Thermodynamic cycle like Otto Cycle, Diesel Cycle, and
their applications in engines etc.
• Understand the application of Thermodynamic cycle etc.
• Understand about process of heat energy being utilized as mechanical
energy in different engines by applying these cycles
6.0 Introduction
Thermodynamics cycle consists of a series of thermodynamics processes,
which takes place in a certain order and the initial conditions are restored at the
end of processes.
Assumption in Thermodynamics Cycles
The analysis of all thermodynamics cycles is based on the following
assumptions:
1. The gas in the engine cylinder is a perfect gas i.e. it obeys the gas laws
and constant specific heats.
2. The physical constants of the gas in the engine cylinder are same as
those of air at moderate temperature.
3. All the compression and expansion processes are adiabatic and they
take place without any internal friction.
4. Heat is supplied by bringing a hot body in contact with the cylinder at
appropriate points during the process. Similarly, heat is rejected by brining a
cold body is contact with the cylinder at these points.
5. It is a closed cycle and the same air is being used again and again and no
chemical reaction takes place.
6.1 Classification of Thermodynamics Cycles
The thermodynamics cycles may be classified mainly as:
1. Reversible cycle
2. Irreversible cycle
1. Reversible Cycle: A process, in which some change in the reverse
direction, reverses the process completely, is known as reversible cycle.
In a reversible process, there should not be any loss of heat due to friction,
radiation or conduction etc. A cycle will be reversible if all the processes
constituting the cycle are reversible. Thus in reversible cycle, the initial conditions
are restored at the end of the cycle.
2. Irreversible Cycle: If in a thermodynamics cycle, the change does not
reverse the process, it is called irreversible cycle. In an irreversible cycle, the
initial conditions are not restored at the end of the cycle.
Types of Thermodynamics Cycles
Some of the important thermodynamics cycles are
1. Carnot cycle
2. Stirling cycle
3. Ericsson cycle
4. Joule Cycle
5. Otto cycle
6. Diesel cycle
7. Dual combination cycle.
Carnot Cycle: This cycle was devised by Sir Nicholas Leonard Sadi
Carnot, who was the first scientist to analyse the problem of the efficiency of a
heat engine.
In a carnot cycle, the working substance is subjected to a cyclic operation
consisting of two isothermal and two adiabatic operations.
The engine imagined by carnot has air which is supposed to behave like a
perfect gas as its working substance enclosed in a cylinder, in which a frictionless
piston ‘A’moves. The walls of the cylinder and piston are perfect non-conductors
of heat. But the bottom ‘B’ of the cylinder is a perfect conductor of heat. The
engine is assumed to work between two sources of infinite capacity, one at
higher temperature and the other at lower temperature.
Now, let us consider the four stages of the carnot cycle. Let the engine
cylinder contain m kg of air at its original condition presented by point 1 on the
p-v and T-S diagram.
At this stage, let P1, T1 and V1 be the pressure, temperature and volume of
the air respectively.
1. First stage: The source (hot body, (HB)) at a higher temperature is
brought in contact with the bottom B of the cylinder. The air expands practically
at constant temperature T1, from V1 to V2. It means that the temperature T2 (at
point 2) is equal to the temperature T1. The isothermal expansion is represented
by curve 1-2 on p-v and T-S diagrams. The heat supplied by the hot body is
fully absorbed by the air, and is utilized in doing external work.
Heat supplied = Work done isothermal expansion.
H1 = P1 V1 loga(V2/V1) = mRT1 (V2/V1) ….. (since P1V1 = mRT1)
= 2.3 mRT1log r.
1. Second stage: The hot body is removed from the bottom of the cylinder
‘B’ and the insulating cap I.C is brought in contact. The air is now allowed to
expand adiabatically.
Thus adiabatic expansion is represented by the curve 2-3 p-v and T-S
diagram. The temperature of the air falls from T2 to T3.
Since no heat is absorbed or rejected by the air, therefore decrease in
internal energy.
= work done by the air.

= (P2V2 – P3V3) (mRT2 – mRT3)
 -1 =  -1
( pv = mRT)
= mR(T1-T2)
-1
3. Third stage: Now remove the insulating cap I.C from the bottom of
the cylinder and bring the cold body CB in its contact. The air is compressed
practically at a constant temperature T3 from V3 to V4. It means the temperature
T4 (at point 4) is equal to the temperature T3. This isothermal compression is
represented by the curve 3-4 on p-v and T-S diagram. During the process, the
heat is rejected to the cold body and is equal to the work done on the air.
Therefore Heat rejected = work done on the air.
H2 = P3V3 loge (V3/V4)
= MRT3 loge (V3/V4)
= 2.3 Mrt3 logr (since r = V3/V4 = compression ratio).
4. Fourth stage: The insulated cap I.C is again brought in contact with
the bottom of the cylinder B and the air is allowed to be adiabatically. The
adiabatic compression is represented by the curve 4-1 on p-v and T-S diagram.
The temperature of the air increases from T4 to T1.since no heat is absorbed or
rejected by the air, therefore
Increase in Internal energy
= work done on the air
= (P1V1 – P4V4)/ã-1
= (mRT1 – mRT4)/-1 (since pv = mRT)
= (mR(T1-T3))/-1 (since T3 = T4)
The decrease in internal energy during adiabatic expansion 2 -3 is equal to
the increase in internal energy during adiabatic compression 4 – 1.
Heat supplied during Isothermal expansion 1 – 2
= H1 = T1 (S2 – S1)
and heat during isothermal compression 4 – 1

= H1 = T4 (S2 – S1) = T3 (S2 – S1)
Work done = heat supplied – heat rejected.
= T1 (S2 – S1) - T3 (S2 – S1)
= (T1 – T3) (S2 – S1)
Therefore efficiency n = work done/heat supplied
= ((T1 – T3) (S2 – S1))/ T1 (S2 – S1)
= (T1 – T3)/T1 = 1 – T3/T1
(p-v and T-S diagram).
6.2 Otto Cycle
This cycle was originally devised by a Frenchman Bean-do-Rochas in 1862.
The first successful engine working on this cycle, was built by a German Engineer,
Nicholas A. OTTO in 1876. It is also known as ‘constant volume cycle engine’
as the heat is received and rejected in a constant volume.
An ideal otto cycle consists of two constant volume and two adiabatic
processes as shown in the p-v and T-S diagram.
1. First stage: The air is expanded adiabatically from initial temperature
T1 to a temperature T2 as per the graph 1.2. In this process, no heat is absorbed
or rejected by the air.
2. Second stage: The air is cooled at constant volume from temperature
T2 to temperature T3 as per the graph 2 -3. We know that heat rejected by the
air during the process,
H2 = mCv (T2 – T3) ……………. (i)
3. Third stage: The air is compressed adiabatically from T3 to temperature
T4 as per the graph 3 -4. in this process no heat is absorbed or rejected by the
air.
4. Fourth stage: the air is now heated at constant volume from temperature
T4 to temperature T1 as per the graph 4 – 1. We know that heat absorbed during
the process
H2 = mCv (T1 – T4)……………. (ii)
We can see that air has been brought back to its original conditions of
pressure, volume and temperature, thus completing the cycle.
Work done = heat absorbed – heat rejected
= mCv (T1 – T4) - mCv (T2 – T3)
Therefore efficiency or air standard efficiency,
 = work done / heat absorbed
= (mCv (T1 – T4) - mCv (T2 – T3))
mCv (T1 – T4)
T2 - T3 T3 (T2 / T3 - 1)
=1- = 1- ............ (iii)
T1-T4 T4 (T1 / T4-1)
We know that from adiabatic expansion process (1-2),
 
T2 V1 1
= =
T1 V2 r
Similarly from adiabatic compression process (3-4)
 
T3 V4 1
= =
T4 V3 r
From the above two equations, we find that

T3 T2 1 1
= = = 
T4 T1 r
(r)
6.3 Diesel Cycle

This cycle was devised by Dr. Rudolph Diesel in 1893. This is an important
cycle on which all the diesel engines work. It is also known as constant pressure
cycle engine a heat is received at constant pressure.
The engine imagined by Diesel has air enclosed in the cylinder, whose walls
are perfectly non-conductor of heat, but bottom is a perfect conductor of heat.
Again there is a hot body and cold body and an insulating cap, which are
alternatively brought in contact with the cylinder.
The ideal diesel cycle consists of two adiabatic, a constant pressure and a
constant volume processes.
Let the engine cylinder contain m kg of air at point ‘t’. At this point, let P1,
T1 and V1 be the pressure, temperature and volume of the air.
1. First stage: The air heated at constant pressure from initial temperature
T1 to a temperature T2 as per the graph 1.2.
Therefore Heat supplied to the air = mCp (T2 – T1) …………. (i)
2. Second stage: The air is expanded adiabatically from temperature T2
to temperature T3 as per the graph 2 -3. In this process, no heat is absorbed or
rejected by the air.
3. Third stage: The air is now cooled at constant volume from temperature
T3 to temperature T4 as per the graph 3 -4.
Therefore Heat rejected by the air = mCv (T3 – T4) …………. (ii)
4. Fourth stage: The air is compressed adiabatically from a temperature
temperature T4 to temperature T1 as per the graph 4 – 1. In this process no heat
is absorbed or rejected by the air.
We see that air has been brought back to its original conditions of pressure,
volume and temperature.
Work done = heat absorbed – heat rejected
= mCp (T2 – T1) – mCv (T3 – T4)
Therefore standard efficiency ç = work done / heat absorbed
= Heat absorbed – heat rejected
Heat Absorbed
= mCp (T2 – T1) - mCv (T3 – T4)
mCp (T2 – T1)
Cv T3 - T4 T3 - T4
=1- = 1 - 1/(iii)
Cp T2 - T1 T2 - T1
Now let compress ratio

r = V4 / V1
Cut off ratio p = V2/V1

Expansion ratio, r1 = V3/V2 = V4 / V2 (Since V3 = V4)
= V4/V1 x V1 / V2 = r x 1/p = r/p
For Constant pressure heating process (1-2)
V1 / T1 = V2 / T2 = ................................ (Charle’s Law)
Therefore T2 = T1 x V2 / V1 = T1 x p ..................... (iv)
Similarly
In adiabatic compression process (2-3)
 

T3 V2 1 p
= = =
T2 V3 r1 r
 
Therefore T2 = T2 (p/r) = T1 x p (p/r)
And in an adiobatic compression process (4-1)

T1 V4
= = (r) ............................ (vi)
T4 V1
Substituting the value of T1 in equations (iv) and (iv)
T2 = T4 (r) x p .......................(vii)
 

and T3 = T1 (r) x p (p/r) = T4 p .......... (viii)
Now substituting the values of T1, T2 and T3 in equation (iii)

( T4 x p ) - T4
n=1-1
 
 ( T4 (r) p - T4 (r)
= 1- 1 pr - 1

r  (p - 1)

1. Define Otto Cycle and draw its P-V diagram
2. Define Diesel cycle and draw its P-V diagram
3. Define Carnot Cycle and draw its PV Diagram
1. Explain Otto cycle with P-V diagram
2. Explain Diesel Cycle with P-V diagram
UNIT 7
Transmission of Power
Learning Objectives
• Understand how the mechanical power is being transmitted,
• Different methods of transmitting power, chain drive, belt drive, rope
drive, their application, how to use them.
• Compound gear drive, and also the uses of Jackey pulley.
7.0 Introduction to Transmission of Power

Power transmission is the movement of energy from its place of generation
to a location where it is applied to perform useful work.
Power is defined as units of energy per unit time.
In SI units
Watt = joule / second = Newton x meter / second.
Mechanical power transmission is used for short distances. Mechanical
power may be transmitted directly using solid structures such as drive shaft,
transmission gears etc. The transmission gears can adjust the amount of torque
or force v/s speed.
A shaft is a rotating machine member usually having a circular cross section

much smaller in diameter than its length. Power transmitting elements namely,
pulleys, belts, ropes, chains, gears etc. are mounted on the shafts.
7.1 Types of Power Transmitting drives
1. Belt drive
2. Rope drive
3. Chain drive
4. Gear drive
7.1.1 Belt Drive
Belts are used to transmit power between two parallel shafts. A belt drive
consists of two pulleys on which belt is passed. One of the pulleys called the
‘driver’ is mounted on the driving shaft, while the other, which is mounted on the
shaft to which power is transmitted is called the ‘driven’.
The diameters of the driving and driven pulleys on the ‘speed ratio’ of the
drive. The power is transmitted from the driver pulley to the driven pulley by the
frictional grip between the belt and the surfaces of the pulleys.
Types of Belts
Based on the cross section of the belts, the belt drives are divided as follows:
Flat belt: It is used in factories, workshops and flour mills for transmitting
a moderate amount of power.
V-belt: It is used for transmitting a moderate amount of power, when the
centre distance between the driver and driven is very less.
Types of Belt drive
a. Open Belt Drive: The open belt drive is used when two parallel shafts
of the driver and driven rotate at the same direction.
The power transmitting capacity of belt drive depends on the tensions in
the tight and slack sides, angle of contact of the smaller pulley (è) and the co-
efficient of friction (µ) between the belt and the pulley materials.
Velocity Ratio: The velocity radio (i) is defined as the ratio of the speed
of the driving pulley (N1 in rpm) to the speed of the driven pulley (N2 in rpm).
Assuming no slip between the belt and the pulleys, the speed at every point in
the belt is same. Therefore the linear squad of the belt and the circumferential
speeds of the driving and driven pulleys are equal.
d1 N1 =  d2 N2
i = N1 / N2 = d1 / d2
where d1 = diameter of driver pulley
d2 = diameter of driven pulley.
Tight side
Assume clockwise rotation of the driver pulley. The driver pulley pulls the
belt from the lower side and delivers to the upper side. Thus the tension in the
lower side belt will be more than that of the upper side belt. Because of the
higher tension, the lower side belt is known as tight side.
T1 = Tension in the tight side
Slack Side
Because of less tension, the upper side is known as ‘Slack side’.
T2 = Tension of the slack side.
b. Crossed Belt Drive
It is used when two parallel shafts of the driver and the driven rotate in the
opposite directions. At the point when the belt crosses, it runs against itself
causing excessive wear. To avoid this, the shafts should be placed at maximum
distance ‘20w’.
Where w is the width of the belt and operated at velocities less than 15m/
sec.
Belt Slip
In flat belt drive, the difference between tensions in tight and slack sides of
the belt is equal to force of friction between belt and pulley. When the frictional
grip becomes insufficient, the belt begins to slide over the surface of the pulley.
This sliding of the belt which causes relative motion between pulley and belt is
called ‘slip’ of the belt.
V-Belt drive: When a belt is trapezoidal in section, designed to run in a
‘V-shaped groove’, it is known as V-belt. The V-belt runs is 30° to 40° vee
grooves in the pulleys. The effect of the groove is to increase the frictional grip
of the V-belt on the pulley and thus reduce the tendency of slipping.
7.1.2 Rope Drive

Rope drive are widely used where the power to be transmitted is more
than 150 KW and centre distance is more than 10m. In spinning mills, where
number of driving pulleys are more, these drives are used. Steel wired ropes are
used in hoisting equipment, craves, elevators, conveyors and other material
handling equipment.
7.1.3 Chain Drive
Chains are made up of rigid links hinged together. Chain drives are positive
drives with no slipping. Hence velocity ratio remains constant. Power transmitted
is as high as 100 KW. Wheels having teeth especially designed for chain are
known as ‘Chain Sprockets’. Chan drive is used when the centre distance is
less as in bicycles, motor cycles, road rollers, agricultural machinery etc.
Gear Drive
Gears are defined as toothed wheels which transmit power from one shaft
to another by means by successive engagement of teeth.
Gear drives are used to transmit moderate or large amount of power
positively over a short distance with a ‘constant velocity ratio’.
Gear Trains
Any combination of gear wheels by means of which power is transmitted
from one shaft to another shaft is called ‘Gear Train’. Usually the ‘train’ is applied
only to combinations, in which there are more than one pair.
Types of gear drive
1. Simple gear drive
2. Compound gear drive
3. Reverted gear drive
4. Epicyclic gear drive
Simple gear drive
A simple gear drive train is one which each shaft carries one gear only.
These are employed where a small velocity ratio is required. When distance
between two shafts is small, gears 1 and 2 are in mesh with each other to transmit
motion from one shaft to the other.
Velocity Ratio = N1 / N2 = T2 / T1
Where N1 and N2 are speeds of drive and driven gears in rlm

T1 and T2 are number of driving and driven gears.
Compound Gear Drive
In a gear train, when the intermediate shaft carries two gears, it is known as
compound gear drive. The compound gear drive is used when the velocity ratio
is so high that one of the gears in the simple gear drive is very small.
Belt Fastener
There are different types of belt fasteners. Some of them are:
a. Plate grip fasteners: These can be used on belts of any width and
varying thickeness.
b. Riv-Nail fasteners: These can be used as synthetic high strength belt
fabrics.
c. Staple grip fasteners: These fasteners are very strong. It’s hinged
plates are held in compression with ‘high tensile stainless steel staples’.
d. Steel grip fasteners: These are having combined toughness and with
ease of installation.
e. Flex grip round belt couplings: These are smooth in operation with
tough grip in multidirectional turns.
7.2 Jackey Pulley
Jackey Pulley is used to maintain tension in a chain or belt by using jackey
wheel. These wheels are used in causes and other pulley equipments.
Summary
Types of Transmission devices
(a) Belt drive
(b) Rope drive
(c) Chain drive
(d) Gear drive
Type of Belt drive
(a) Flat belt drive
(b) V- belt drive

1. Mention the types of power transmitting drives.
2. Mention the types of belt drives
3. Mention the types of Gear drives
1. Explain different types of power transmitting drives.
UNIT 8
Fasteners
Learning Objectives
• Understand Fasteners and different types of fasteners
• Understand about Nuts, Bolts, Rivets, Welding application in
engineering usage.
8.0 Introduction
Fastener is a hardware device that mechanically joins or affixes two or
more objects together. Screws, nuts and bolts, rivets, clamps etc are different
types of Fasteners used in mechanical engineering application.
Screws
A screw is a type of fastener characterized by a helical ridge, known as an
external thread often in the form of a nut or an object that has the internal thread
formed into it.
Nut & Bolt
A nut is a type of hardware fastener with a threaded hole. Nuts are almost
always used opposite a mating bolt to faster stack of parts together. Nuts are
graded with strength ratings compatible with their respective tools.
Bolt is a type of joint which is the common element in construction and

machine design. They consist of fasteners that capture and join other parts and
are secured with mating of screw threads.
Rivet
Rivet is a permanent mechanical fastener. A rivet consists of a smooth
cylindrical shaft with a head on one end. The end opposite to head is called the
buck-tail. On installation, the rivet is placed on a pre-drilled hole, and the tail is
upset or bucked so that it expands to about 1.5 times the original shaft diameter.
It can support tension loads.
Clamps
Clamps are fastening devices to hold or secure objects tightly together to
prevent movement or separation through the application of inward pressure.
Some clamps are temporary and they are used to position components
temporarily for various tasks.
Some changes are permanent like Hose clamps, Marman clamps, Wire
rope clamps etc.
1. Define Fastener
2. Define Screws
3. What is the usage of Nut and Bolt
4. What is the purpose of Rivet.
5. Why clamps are used.
1. Explain different fasterners and their usage.
UNIT 9
Units of Mechanical Work, Power
and Energy
Learning Objectives
• Understand Work, Power, Energy and their units
• Types of Energy and their application in engineering usage.
9.1 Introduction
The mechanical terms of work, power and energy are related to the work
done by the force and the energy is this related process are the important terms
relating to a similar work.
Work
It is a scalar quantity and is the product of force of magnitude ‘F’ acts on a
point that move ‘d’ distance in the direction of force, then the work ‘w’ done by
this force is calculated as w=Fxd.
The rate of work done by a force measured in Joules/scond or watts. It is
a scalar product. The work done by a force of one Newton acting over a
distance of ‘1 metre’.
Power
Power is the rate at which the energy is transferred.
Energy transfer can be used to do work, so power is also the rate at which
the work is performed.
The S.I Unit of power is ‘Watt’.
1 Watt=1 Joule/second
The mechanical power is combination of force and movement.
It is the product of a force on an object and the velocity of the object or the
product of a torque on a shaft and the angular velocity of a shaft.
Energy
It is the ability of a physical system which is to do work on other physical
systems.
The total energy contained in an object is identified with its mass.
The energy cannot be created or destroyed.
It may be stored in system without being present in the matter.
It is the sum of energy of potential and kinetic energies.
The potential energy is the energy of the position and the kinetic energy is
the energy developed by the motion or movement of the object.
K.E=1/2 mv2

1. Define work and mention its units.
2. Define Power and mention its units
3. Define Energy and mention its units.
4. Mention the types of energy
1. Mention and explain the work, power , energy with their units.
UNIT 10
Safety Precautions
Learning Objectives
• Know about the safety precautions while doing different works in
electrical field.
• Causes of electrical shocks and their treatment
• Prevention of electrical Shocks
10.1 Introduction
Safety ‘ plays an important role in doing electrical jobs where extreme care
has to be taken in performing certain works on live wires of electricity. A little
carelessness causes electric shock which may cause an injury or death as the
severity of electric shock increases. Due to these reasons, atmost care has to
be taken while doing electric workers. Even though, after taking some
precautions, a little carelessness causes electric shock.
Then certain first aid measures are to be taken.
10.1 Precautionsin Handling Tools
The most commonly used tools by an electrician are
i). Screw driver
ii). Pliers
iii). Bradawl
iv). Gimlet
v). Chisels
vi). Saws
vii). Hammers
viii). Electric Knife
ix). Hand drilling machine
x). Files
xi). Vices
xii). Soldering Iron etc
While working with the above tools in an electrical work, the following
precautions to be taken.
1. Use proper tools for each job.
2. Don’t use hammeter on the head of the screw driver.
3. While removing Nuts and Bolts, only spanners are to be used but not
pliers.
4. Protect the tools againist must.
5. A tool with properly fixed handle is to be used.
6. Pointed tips and insulated handles should not be damaged.
7. The tools should not be placed in a haphazerd way.
8. Proper precautuionary instructions should be placed on the job whil
working on it.
9. Drilling tools should be driver straight.
10. Throughly clean the tools before using, so that oil or grease should not
be present on them.
11. Dont’t cut the wires with plier. Only cutter is to be used for it.
12. Before doing any job on live wire, the tools should be properly insulated.
13. The handles of chisels, hammers, saws etc. Are properly fixed.
14. The wire gange and wire handles are to be fully clean while working on
them.
15. Always be sure of proper safety while woring.
10.2 Causes of Electric Shock
The electric shock may be caused due to the following reasons.
1. The electric wires through which the current passes are not properly
insulated.
2. There may be loose contact between any two wires.
3. There may be water or moisture surrounding the live wires.
4. The person who is working with wires is not properly insulated for his
safety.
5. The earthiry, positive and negative wires are not properly connected
accordingly
6. The connection from transformer to main connection are not in proper
manner.
7. If the careless are not according to the recommendaion of the load, they
may melt and it causes shock.
8. Always use recommended gaused wires.
10.3.1 Cure of Electric Shock
If a person gets electric shock or gets contact with live wire, first switch off
the main switch where the current passes to him. It is not in easily approach to
you, then
1. Pull the victimwhile keeping yourself insulated by wrapping a dry and
thick paper or cloth on your hands.
2. If the victim’s clothes are dry then you may remove him from electric
contact by pulling the edges of his clothes.
3. A dry wooden stick or a light wooden place may be used to remove him
from the electric contact.
Always remember that while removing the victim from the electric contact
other wise you may also get an electric shock.
10.3.2 First Aid to Victim of Electric Shock

(i) If the victim of electric shock is senseless, then lay him down immediately
on a dry wooden place or on a dry led so that the electricity stored in his body
may finish.
(ii) Never lay him down on the ground because it may be possible that he
may not regain sense.
(iii). Extinguish any fire or flame that may be present in his clothes.
(iv). Apply coconut oil the burnt parts.
(v). Do not give any food to the victim without the consultationof doctor.
If necessary, fresh water may be given if the patient is concious.
(vi). Keep the victim covered with blanket, so that he may not catch cold.
(vii).Watch that he is breathing properly or not. If he is not breathing properl,
artificial registration may be given to him as first aid.
10.3.3 Methods of Artificial Respiration
There are two main methods of artificial respiration.
(i) Sylvestor’s method
(ii) Schaffer’s method
10.3.3.1 Sylvestor’s Method
If there are burns on the chest of victim, then lay down him on his back.
Looser the clothes and put a pillow beneath his showlders, so that his chest may
raise upwards. Open the victim’s to allow the fresh air to get into his lungs.
First Position
Sit on your knees near the victim’s head, hold his both hands and spread
them wide.
Second Position
Apply some preassue on his hands in the first position. So that the lungs
can discharge their inside air release the after 2-3 seconds and bring the victim’m
hands in the previous position. Now fresh air into the lungs of the patient.
By repeating above actions, the victim starts breathing. While the artificial
respiration procedures are in continuaion, keep the victim’s mouth also open, so
that the air passage reamains clear. The whole position should not be repeated
10-12 times per minutes.
For complete relief, the arfificial respirationshould be continued for 1-3
hours.
10.3.3.2 Schaffer’s Method
If the burns on the back of victim, them lay him down with his chest
downwards. Loose or remove his clothes, rest his face on to one side, spread
his pillow beneath his chest so that his back rises upwards shightly.
First Position
Kneel over the patient’s back and place your both hands on his back near
the lowest rib is such a way that the fingers are spread outwards while the two
thumbs almost touch each other and remain parallel to the spire.
Second Position
Apply some preassure at the victim’s back while keeping your hands straight.
Rock yourself forward gently. After 2-3 seconds, release the pressure slowly
and return to the first position by shiding your palms sideways. Repeat the
process for about 12-15 times a minute. It will expand and contract the lungs of
the victim and thus will help the victim in breathing. A victim may require 1-3
hours for reestallishing his nature breathing.
10.4 New Methods of Artificial Respiration
The new methods of artificial respiration are comparativelyeasier and help
the victim to get normal breathing repidly.
These are as under
(i) Mouth to Mouth Method
In this method, the air is filled into the victim’s mouth by blowing with your
own mouth.
Lay down the victim on his back. Loose his clothes. Put a pillow beneath
his neck so that his head is titted backwards. Open the victim’s mouth and
clean it with your finger.
Now put your one hand under the victim’s neck and second hand on his
mouth such a way that his mouth remains open. Now take a deep breath, keep
your lips on the victim’s lips and blow the air with a force into the mouth while
keeping his nose shut. The air is filled into his lungs by this procedure. Now
remove yout mouth so that the lungs can discharge the inside air. Repeat the
above action10-12 times a minute.
As a precaution, you may be use a clean and fine cloth piece between the
two mouths while blowing the air into the mouth.
(ii) Mouth to Nose Method
If it becomes different to given the victim’s mouth then apply mouth to nose
method.
Lay down the victim on his back. Loose his shirt put a pillow beneath his
neck so that his head his is filted backwards. Now blow the air into his nose
while keeping his mouth closed. Remove your mouth from his nose so that the
lungs can discharge the inside air. If the blown in air does not enter the lungs,
then shake his shoulders. The whole action is repeated 10-12 times a minute. A
piece of time and clean cloth may be used between his nose and your mouth.
Summary
1. Always use properly insulated and greaded wires and cables according
to the requirements of connections.
2. Never use loose connections between any two live wires.
3. Use proper insulated tools while working an electric live wires.
4. Always the cautions in connecting wires.
5. Proper safety measures to the followed while connecting terminals.
6. First aid measures are to be followed if any person gets electric shock.
1. What are the commonly used tools of an electrician?
2. What will you do, if any person is shocked by electric current?
3. Write briefly about Electric shock?
4. What is artificial respiration?
1. What are the safety precaution while working on an electric job?
2. What are the causes of electric shock?
3. Mentain the artificial respiration methods and explain any one method?
UNIT 11
Electric Current, Ohm’s Law,
Kirchoff’s Laws
Learning Objectives
• Understand electric laws like Ohms law, Kirchoff’s law
• Definitions like conductors, semi conductors, insulators, voltage,
resistance etc.
• Know about specific resistance and its units.
Introduction
The fact that amber, when rubbed, was capable of attracting light objects
was known to the Greeks 2500 years ago. Thales of Miletus become aware of
this peculiar properly in 600 B.C.
William Gilbert (1544-1603), who was the physician of Queen Elizibeth,
made further investigations and learned that many substances besides amber
attracted other objects when activated by friction. He called such attraction
‘electric’ after the Greek word ‘electric’ meaning amber.
In 1729 Stephen Gray found that when substance has been electrified by
friction and then was allowed to touch another substance the power of attraction
was passed to the seond substance seven years later, desgauliers, pointed out
that same substances possessed the ability to transmit the attractive from one
point to another. He called such substances concuctors. The other substances

which are not having such properly are called insulators.
11.1 Electric Current
The rate at which the electrons move or flow along the wire gives the strenght
of the current. Current is represented by the letter symbol “I” ans is measured
in amperes (A).
Voltage
The force that tends to cause the free electrons to move from the negative
to the positive end of the wire is called ‘electron moving force’ or ‘electro motive
force’. It is denoted by EMF or ‘Voltage’ or ‘potential Difference’.
11.2 Conductors, Semi - Conductors, Insulators
The continuous flow of electrons constitutes an electric current. It is found
that those substances whose atoms have their outer most orbits incomplete act
as good conductors of electricity. i.e. they permit an easy detatchment of their
outermost electrons and offer very little hinderance. Such substances are known
as good conductors.
But substances whose electrons are rigidly held to their atoms are called
‘Bad conductors’ materials like germanium, silicon, silcon carbide etc. Whsoe
resistances at ordinary temperature lie in between those of typical metals and
typical insulators are called semi - conductors.
11.3 Conventional Electric Current Flow
In a simple voltaic cell, there is a copper plate (known as anode) and a zinc
rod (i.e cathode) immersed in dilute sulphuric acid (H2So4 )
Direction of electron flow
Cu
Zn
Fig. 11.1 Conventional Direction of Current

contained is suitable vessel. The chemical action taking place within the
cell causes the electrons to be removed from Cu plate and is to deposited on
Zinc rod at the same time. This transfer of electrons is accomplished through
the agency of the diluted H2So4.
Which is known as electrolyte. The Zinc rod becomes negatigative due to
the deposition of electrons an it and the Cu plate becomes positive due to the
removal of elctrons from it. Then the electrons move from -Ve terminal to +Ve
terminal is called conventional electric current.
The rate at which the electrons flow or move along the wire gives the current
strength or simply ‘current’ and is represented by the letter’I’ and is measured in
ampered (A).
11.4 Idea of Electric Potential
The force that tends to cause the force electrons to move from the negative
to the positive end of the wire is called electron moving force or potential
difference. It is known as voltage and measured in volts (V).
11.5 Definition of Electrical Resistance Unit
The properly of a substance / material due to which it opposes the flow of
electrons (current) through it is called resistance. The resistance is represented
by the latter ‘R’and is measured in Ohm.
11.6 Calculation of Resistance of a Conductor
The resistance a material depends upon the following factors.
i). The resistance of a conductor is directly proportional to its length -‘l’.
i.e. R l
ii). The resistance of a conductor is inversely proportional to its cross
sectional area- ‘a’.
i.e. Ra
iii). The resistance of a conductor depends upon the material with which it
is made. Various substances havedifferent atomic structure and therefore they
offer different resistance for the same length and area of cross section.
iv). The resistance of a conductor depends upon the working temperature
.
i.e. R  l/a
or R= l/a
When p (Greek letter ‘Rho’) is proportionality canstant and is called
resistivity or specific resistance.
11.7 Definition of Specific Resistance - Unit
The specific resistance may be defined as the resistance of a material of
unit length ans of unit cross sectional area. i.e. the resistance between the opposite
faces of a unit cube is
R =l/a
= Ra/l=dim x m2/m=dim-m.
Hence the specific resistance is measured in dim-material /Ohm-cms / micro
Ohm-m etc.
11.8 Simple Problems
Example 1
Determine the resistance of a 564 m length of aluminium conductor whose
regular cross section is 4 cm by 2cm .
Take =2.826x10-8-m
Solution:
Given data
l=564m.
b=2cm=0.02m.
t=4cm=0.04m.
=2.826x10-8m.
Cross sectional area, a=bxt
= 0.02x0.04
= 0.0008m2
= 8x 10-4m2
R = l/a = 2.828x10 -8 x 564/8x10-4
= 0.02 
Example 2
Calculate the length of copper wire, 1.5 mm in diameter to have a resis-
tance of 0.3 ohm given the resistivity of copper is 0.017 micro-ohm-metre
Solution:
Given data
d = 1.5 x10-3
R = 0.3 

l=?
Cross sectional area of wire
A = x d2
= x=
= 1.767 x 10-6 m2
R = l/a
l = 0.3 x 1.767 x10-6/0.017 x 10-6
l = 31.185 m
11.9 Effect of Temperature on Resistance
Connect a tungsten filament lamp across a battery. The voltmeter across
the lamp given the potential across it. By varying the number of cells in the
circuit, the current taken by the lamp.
It can be proved that the resistance of most of the metals increase with
temperature.
When a potential in applied to the ends of a cnductor, the current flows.
The movement of electrons is opposed by ions of the materials. At lower tem-
perature these ions are assumed to be stationay. But as the temperature of the
material increases, these ions gain energy and oscillate about their mean posi-
tion. The amplitute of these osciallation is dependent upon the temperature of
the material. Higher the temperature the greater is the amplitude of oscillation.
The random movementof ions opposes the electron movement and increases
the chances of collision.
Hence due to increase of this opposition to the movement of the electrons,

the resitance of the conductor increases.
If the temperature of the conductor decreases , the amplitude of the con-
ductor and the chance of collision of electrons decreases and hence the resis-
tance of the conductor decreases the resistance in temperature.
11.10 Temperature Co-efficient of Resistance
The temperature co-efficient of resistance is not constant at all tempera-
tures. For determining the resistance at intial temperature the temperature co-
efficient at intial temperature should be used. In order to develop a relation
between temperature co-efficient at different temperature.
Let us consider a conductor having
R0 = Resistance at 00C
R1 = Resistance at t10C
R2 = Resistance at t20C
0 = Temperature co-efficient at 00C
1 = Temperature co-efficient at t10C
then R1 = R0 (1+t1) and ---------- (I)
R2 = R0 (1+t2) -----------(II)
(Since intial temperature is 00C, 0 is to be taken )

Divide the Equation II with Eq I.
R2/R1 = 1+t2 /1+t1 ------------(III)
Using Binomial theorem for expansion and neglecting higher power of (t1)
we can write
= 1+(t2-t1)
R2 = R1(1+ (t2-t1) ) ---------(IV)
Now to find the R2 at t20 C from the intial temperature t10 C, temperature
coefficient used must be at t10 C.
R2 = R1((1+ (t2-t1) ) ---------(V)
or
R2/R1 = ((1+ (t2-t1) ) ---------(VI)
Equating equation III and VI
1+t2/1+t1 = 1+(t2-t1)
(t2-t1) = 1+t2/1+t1 -1
= 1+t2-1-t1 /1+t1
= t2-t1/1+t1
(t2-t1) = (t2-t1) /1+t1
 1+t1

It is the telation between temperature coefficient at 00 C and t10 C

 1+t1

11.11 Ohm’s Law

This law applies to electric conduction through good conductors.
It can be stated as
“The ratio of potential difference (V) between any two points on a conduc-
tor to the current (I) flowing between them, is constant, provided the tempera-
ture of the conductor does not change”.
In other words
“The current flowing in a current is directly proportional to the potential
difference, provided the temperature is constant”.
i.e.V/I = Constant
or
V/I = R
Where R is the resistance of the conductor between the two points.
11.12 Resistances in series
When some conductors having resistances R1, R2and R3 etc are joined end
to end, they are said to be connceted in series. It can be proved that the equiva-
lent resistance between the points A and D is equal to the sum of the three
individual resistances.
Figure
Being is series circuit
i). Current is the same through all the three conductors.
ii). But voltage drop across end is different due to its different resistance
and is given by ohm’s law.
iii). Sum of three voltage drops is equal to the voltage applied across the
conductors.
V = V1+V2+V3 ------ = IR1+IR2+IR3+-----
(According to the ohm’s law)
Where R is the equivalent resistance of the series combinations
IR = IR1+IR2+IR3+---
R = R1+R2+R3+----
Resistances in Parallel
Three resistances are connected in parallel.
In this case
i). Potential difference across all resistances is the same.
ii). Current in each resistor is different and given by ohm’s law.
iii). Total current is the sum of the three currents.
I1 R1
I2 R2
R3
I3
V
I = I1+I2+I3
I = V/R1+V/R2+V/R3
Now I = V/R where V is applied voltage.
R = Equivalent resistance of parallel combination.

There fore V/R = V/R1+V/R2+V/R3
or
1/R = 1/R1+1/R2+1/R3
Resistance in Series and Parallel Combination
Sometimes the circuits may be neither pure series nor pure paralles, not a
combination of series and parallel may come across. For such circuits, first
parallel combination of resistance R1 and R2 should be solved for finding
its equivalent resistance Re.
R1
R3 R2 R3
R2
V
V
1/Re = 1/R1+1/R2
or
Re = R1R2/R1+R2
Then the equivalent resistance Re and R3 from a series circuit.
Thus the resul that resistance is the total of resistance of Re and R3.
Solved Problems
1. Calculate the effective resistance of the following combination of the
resistance and the voltage drop across each resistance when 60 V is applied.
Figure
Solution
Given data
R1 = 3 
R2 = 6 
R3 =18 
R4 = 5 
V = 60 v
R=?
V1, V2, V3 = ?
Resistance between the points A and B is
RAB = R1x R2/ R1+R2
= 3x6/3+6
= 18/9
RAB
RAC = RAB +R3
= 2+18
RAC = 20 
Effective resistance of the combination is
R = RPQ
= 20x5/20+5
= 100/25
R =4
Total Current
I = V/R
= 
mps
Current in 5  resistor =V/R4 = 60/5 = 12 Amperes
Current through AC (i.e.RAB and R3) is 15-12= 3 Amperes.
There fore drop across R1 and R2 combination = 3x2 = 6 volts
Voltage drop across R3 =3x18 =54 Volts.
Voltage drop acorss R4 = 12x5 =60 volts.
2. In the circuit given below calculate the voltage across 10 

resistance.
14 2
10
6 8
14
25V
Solution
14 and 6 resistors are in parallel.
Their equivalent = 14x6/14+6
= 84/20
= 4.2 
Similarly 2 and 8 are in parallel
Their equivalent = 2x8/2+8


(4.2+1.6) and 4.2 are in parallel.
= (4.2+1.6) x 4.2/(4.2+1.6)+4.2
= 2.436
Total resistance of the circuit RT = 2.436+10
= 12.436 
Total amount I = V/R
= 25/12.436
= 2.0103 A
Voltage across 10  resistor
= I x10
= 2.0103 x10
Voltage across 10 resistor = 20.103 volts
Kirchoff’s Laws
These laws are used for solving electrical networks. These laws are par-
ticularly useful in determining the equivalent resistance of a complicated net-
work of conductors and for calculating the current flowing in the various con-
ductors.
i) Point Law or Current Law
(Kirchoff’s First Law)
It states as follows
“In any electrical network, the algebmic sum of the current meeting at a
point or junction is zero.
In case of a few conductors meeting at a point A. Some conductors have
currents leading to point A where as some current leading away from point A.
Assuming the incoming currents to be positive and the out going currents
negative.
I1+(-I2)+(-I3)+(I4)+(-I5)=0
I1-I2-I3+I4-I5=0
i.e  I = 0 at a junction
I1
I2
A
I5
I3
I4
ii) Mesh Law or Voltage Law

(Kirchoff’s Voltage Law)
It states as follows
“The algebmic sum of the products of currents and resistances in each of
the conductors in any closed path (or mesh) in a network plus the algebmic sum
of the e.m.f’s is that path is zero” .
 I R+  e.m.f =0 round a mesh
Energy
The total amount of work done in an electric circuit is called electrical
energy.
i.e. Electrical energy = Total work done in electric circuit.
It is measured by the product of power and time.
Electric energy = Power x time
= VI x t
= V I t watt-second (Since p=VI)
= I2R t watt-second
Key Concepts
Electric Current
The rate at which the electrons flow or move along the wire gives the cur-
rent.
Voltage
The force that tends to cause the free electrons to move the negative to
positive end of the wire is called electron moving force or voltage or potential
difference.
Resistance
The property or a substance / material due to which it opposes the flow of
electrons (current) through it is called resistance. It is represented by the letter
‘R’ and measured in Ohm().
Specific Resistance
It is the resistance of a material of unit length and unit cross-sectional area
Ohm’s Law
The current flowing in a circuit is directly proportional to the potential dif-
ference, provided the temperature is constant.
I V
or
I =V/R
Kirchoff’s Point Law (or) Current Law
In any electrical network, the algebric sum of the currents meeting at a
point or junction is zero.
Kirchoff’s Mesh Law or Voltage Law
The algebraic sum of products of currents and resistances in each of the
conductors in any closed mesh in a network plus the algebraic sum of the e.m.f’s
in that path is zero.
Work
Work is said to be done in an electric circuit when, Q ampere second of
electricity pass through a circuit against a potential difference of V volt.
Power
Electrical power is the rate at which work is done is an electric circuit.
Energy
The total amount of work done in electric circuit is called electrical energy.
1. Define Electric Current?
2. Define Voltage?
3. State Ohm’s Law?
4. Mention Kifchoff’s Point Law?
5. Mention Kirchoff’s Voltage Law?
1. Explain Electrical Work, Power, Energy with their units?
2. Explain Kirchoff’s Laws?
UNIT 12
Electrical Measuring
Instruments
Learning Objectives
After studying this unit, the student will be able
• Understand different measuring instruments used in electricity
• Understand the working of volt meter, Ammeter, watt meter, energy
meter, megger, continuity tester etc.
• Able to know about their usage and their maintenance
12.0 Introduction
The various electrical measuring instruments are being used in the field of
electricity which are to know about the levels of voltage, resistance, capacity of
battery, multimeter testing, energy levels of battery, AC containments testing
etc. While working an electricity, one should know the actual position of elec-
tricity. How it is being passed etc. For this purpose the different meaning
instruments are used.
12.1 Classification of Electrical Measuring Instruments
The principle of working of all electrical measuring instruments depends

upon various effects of electric current or voltage.
Sl.No. Effect of Electricity Type of Instrument Suitable for
1. Magnetic Effect Ammeters, voltme- D.C. and A.C
ters, watt meters and Current
energy meters
2. Electro dynamic effect Ammeters, voltme- D.C and A.C Current
ters, watt meters
3. Electro magnetic induc- Ammeters, voltmeters A.C Current only
tion effect watt meters and en-
ergy meters
4. Thermal effect Ammeters, voltmeters D.C and AC current
5. Chemical Effect Ampere-hour meters D.C only

6. Electrostatic effect Volt meters D.C and A.C current
12.2 Ammeters and Voltmeters and their Applications

There are two basic types of these instruments i.e. attraction type. The
operation of attraction type depends on the attraction of a single piece of soft
iron into a magnetic field and that of repulsion type depends on the repulsion if
two adjustment pieces of iron magenetised by same magnetic field. For both
types of these instruments the necessary magnetic field is produced by the am-
pere turns of current carrying coil.
In case the instrument in to be used as an ammeter, the coil has compara-
tively few turns of thick wire so that the ammeter has low resistance because it
is connected in series with the circuit.
In case it is used as a voltmeter, the coil has high impedance so as to draw
as small a current as passive since it is connected in parallel with the circuit.
The ammeter shows the capacity of battery in ampere’s and voltmeter shows
the voltage or potential difference capacity of the battery.
A voltmeter is an instrument used to measure voltage. When the connec-
tions are made, the voltmeter shows the voltage of the battery. These are de-
signed as a special sort of ammeters which can calculate the voltage by assess-
ing the electrical current and applying ohm’s law.
12.3 Moving Coil Meters and Moving Iron meters

Moving coil meters or instruments are used where high level of accuracy is
needed due to sensitive and accuracy, the moving coil instruments are used.
i). In the measurement of direct current and voltages.
ii). In D.C galvanometers to detect small currents.
iii). In conjuction with rectifiers or thermo junction for A.C measurements
over a wide range of frequencies.
iv). Due to self shielding magnets mechanism there are particularly used in
aircraft and aerospace applications.
Moving Iron Instruments
Basically these instruments are of two types
a). Attraction type moving iron instruments
b). Repulsion type moving iron instruments
a) Attraction type moving iron instruments
It works on the principle of attraction of a single piece of soft iron into a
magnetic field. It consists of a fixed coil or solenoid through which the current
passes. An ovel shaped soft iron is attached to the spindle in such a way that it
can move in and out of the coil. A pointer is attached to the spindle. When the
instrument is connected to the circuit to measure the current or voltage, the
opening circuit flows through the coil. The coil behaves like a magnet when
current passes through the coil. It attaches the soft iron piece towards it and
provide defecting torque(Td).
b) Moving Iron Type (Repulsion Type)
It works on the principle of magnetic repulsion. When two adjustments
iron pieces are magnetized by the same magnetic field, these will be magnetised
with similar polarities and pole strength. Hence because of same polarity, these
will experience a force of repulsion.
12.4 Method of Connecting Ammeters and voltmeters
The majority of Ammeters are either connected in series with the circuit
carrying the current to be measured or have their shunt resistors connected
similarly in series.
The current passes through the meter through its shunt. They must not be
connected to a source of volt. They are designes for minimal burden, which
refers to the voltage drop across the Ammeter.
The Voltmeter can be connected with two wires to where the voltage is.
One wire to positive one and the other the negative. With same voltmeters, one
must make sure that the wires are connected right; the positive connection of
voltmeter to the positive part of the voltmeter source; and the negative to is
parallel to the electric circuit.
12.5 Watt Meter
It is an instrument to show the consumption of electric power or supply
state of electrical energy in the circuit. This instrument is used while measuring
electrical energy in Watt hours which accumulates or averages readings. It can
display may parameters and can be used where a Watt Meter is needed - volts,
current in amperes.
12.6 Energy Meter
It is an electrical measuring device which is used to record electrical energy
consumed over as specified periods of time in terms of units.
12.7 Power Factor Meter
The power factor of an A.C electric power system is defined as the ration
of real power flowing to the load to the apparent power in the circuit. Real
power is the capacity of the circuit for performing work in a particular time.
Apparent power is the product of the current and voltage of the circuit.
The power factor meter measures the power factor with the method of
Wattmeter - Ammeter - Voltmeter method.
A direct reading power factor meter can be made with a moving coil meter
of electrodynamic type, carrying two perpendicular coils on the moving part of
the instrument.
12.8 Megger
It is a portable instrument used for testing the insulation resistance of a
circuit and for measuring resistance of the order of megohms. Which are con-
nected across the outside terminals.
Working Principle
In a cross coil type megger, two coils A and B are mounted rigidly at right
angles to each other on a common axis and free to rotate in a magnetic field.
When currents are passed through them, the two coils area acted upon torque
of coil A is proportional to ‘I1cos‘ and that of coil B is proportional to ‘I2cos(90-

)’ or ‘I2sin’. The two coils come to a position are opposite of equilibrium
where the two torques are opposite and equal.
I1cos = I2sin
or
tanI1I2.
Whenever a current carrying conductor placed in a magnetic field, a torque
is produced on the conductor which tends to rotate it.
X
Magnet (N)
R1 (infinity)
Handle
Testing Terminals Iron Ring
Scale
Pointer
R2
C.C
Y Hand driven D.C.
Generator
0 (Zero)
12.9 Continuity Tester

It is an item of electrical testing equipment which is used to determine if an
electrical path can be established between two points is an electric circuit.
The circuit to be tested completely generalized prior to connecting. The
apparatus. The tester consists of an indicator connected in series with the source
of electric power.
12.10 Measurement of Insulation Resistance
Insulation resistance test is required by the electrical safety standards. It
consists of a gear in resistance of a device while phase and neutral are con-
nected together. The measured resistance has to be higher than the indicated
limit from the international standard. It is used to measure the Ohmic value of an
insulator.
Key Concepts
As per the effect of electricity the electrical measuring instruments are clas-
sified.
Magnetic effect - Ammeters, Voltmeters, Wattmeters,
Energy meters.
Electro dynamic effect - Ammeters, Voltmeters, Wattmeters.
Electro magnetic effect - Ammeters, Voltmeters, Wattmeters,
Energy meters.
Thermal effect - Ammeters, Voltmeters.
Chemical effect - Ampere ohmmeter.
Electrostatic effect - Voltmeters.
Ammeter
An ammeter is a measuring instrument used to measure the electric current
is a circuit. Electric currents are measured in amperes (A).
Voltmeter
A voltmeter is an instrument used for measuring electrical potential differ-
ence two points in and electric current.
Wattmeter
It is an instrument to show the consumption of electric power and measure
energy is watt ohms.
Energy Meter
It is an electrical measuring device which is used to record electrical energy
consumed over a specified period of time in terms of units.
Power Factor Meter
It measures the proper factor with the method of wattmeter- ammeter-
voltmeter.
Megger
It is used for testing the insulation resistance of a circuit and for measuring
resistances in mega ohms.

1. What are the types of electric measuring instruments?
2. Define Ammeter?
3. Define Voltmeter?
4. Define Energymeter?
5. What is the purpose of megger?
1. Briefly explain the connecting of Ammeters and Voltmeters?
2. Explain the Working Principle of Megger?
3. Differentiate moving coil moving Iron instruments?

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126 Automobile Engineering Technician

Working Fluid: It is a fluid on which the Thermodynamic processes are

1.2.1 Types of Thermodynamic Systems

1.4 Definitions of Some of the Properties

Specific volume, v = V/m m3/kg

1.4.9 Internal Energy

Cv= Specific heat at constant volume

Flow of work = Force x displacement

1.5.2 Specific Heat

Long Answer Type Questions

1. Mention the types of Thermodynamic system and explain them

2.1.1 Boyle’s Law

2.1.2 Charle’s Law

(a) Constant pressure (b) Constant Volume.

2.1.3 Avogadro’s Law

Mathematically dE dT = m.c. dT

2.2.2 Characteristic Gas Equation

2.3.1 Specific Heat at Constant Volume

M = Mass of the gas

 Total heat supplied to the gas at constant volume

2.3.2 Specific Heat At Constant Pressure

Let m = mass of the gas

 Total heat supplied to the gas, at constant pressure,

T1 = Initial Absolute temperature or the gas

 M. CP (T2-T1) = P(V2-V1) + M.CV (T2 - T1) ………(iv)

M CP (T2-T1) = m.R (T2-T1)

Then decrease internal energy = dE= mcv dT

(i) Pressure exerted by the gas

Short Answer Type Questions

3.1.2 First Law of Thermodynamic

According to Kelvin - Plank, ‘It is impossible to construct an engine working

2. Constant pressure process

Fig. 4.1 P-V diagram

4.1.2 Constant Pressure Process

Hence, during Isothermal expansion of a gas, Heat added = Work done by

Let V1 = Initial volume of gas

Therefore the work done, W = Area under the curve AB

=  p.dv .............. (i)

Using logarithem table

1. No heat enter or leaves the gas.

Let V1 = Initial volume of gas

from general gas equation, we know that

From general gas equation P1 V1 / T1 = P2V2 / T2

Work done by the Gas :

But we know that the process follows

C.V2 -  C.V1-

P2 V2 V2-  P1 V1 . V1

4.1.5 Polytropic Process

As per polytropic law PVn = C Since P = C / Vn

V2 -n+1 - V1 -n+1 C V2 -n+1 - CV1 -n+1

3. Isothermal Process : A process in which the temperatuer of working

5.2.1 (e) Anthracite Coal

• Risk of fire is minimum.

iv) Better content of consumption by using valves.

Gross or Higher Calorific Value:

b. Premium grade fuel

It should produce least quality of smoke and gases

= work done by the air.

and heat during isothermal compression 4 – 1