Physics Notes Class 11 CHAPTER 12: Thermodynamics
Physics Notes Class 11 CHAPTER 12: Thermodynamics
Physics Notes Class 11 CHAPTER 12: Thermodynamics
Heat
Heat is a form of energy called thermal energy which flows from a higher temperature body to
a lower temperature body when they are placed in contact.
Heat or thermal energy of a body is the sum of kinetic energies of all its constituent particles,
on account of translational, vibrational and rotational motion.
1 cal = 4.18 J
1 calorie is the quantity of heat required to raise the temperature of 1 g of water by 1°C.
J is a conversion factor (not a physical quantity) and its value is 4.186 J/cal.
Temperature
Temperature of a body is the degree of hotness or coldness of the body. A device which is used
to measure the temperature, is called a thermometer.
Highest possible temperature achieved in laboratory is about 108 while lowest possible
temperature attained is 10-8 K.
Branch of Physics dealing with production and measurement temperature close to 0 K is known
as cryagenics, while that deaf with the measurement of very high temperature is called pyromet
Temperature of the core of the sun is 107 K while that of its surface 6000 K.
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1. Celsius Scale In this scale of temperature, the melting point ice is taken as 0°C and the
boiling point of water as 100°C and space between these two points is divided into 100
equal parts
2. Fahrenheit Scale In this scale of temperature, the melt point of ice is taken as 32°F and
the boiling point of water as 211 and the space between these two points is divided into
180 equal parts.
3. Kelvin Scale In this scale of temperature, the melting pouxl ice is taken as 273 K and
the boiling point of water as 373 K the space between these two points is divided into
100 equal pss
Thermometric Property
The property of an object which changes with temperature, is call thermometric property.
Different thermometric properties thermometers have been given below
where p, p100. and pt, are pressure of a gas at constant volume 0°C, 100°C and t°C.
A constant volume gas thermometer can measure tempera from – 200°C to 500°C.
Rt = R0(1 + αt + βt2)
Rt = R0(1 + αt)
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lt = l0(1 + αt)
where α = coefficient of linear expansion and l0, lt are lengths of mercury column at 0°C and
t°C.
When two junctions of a thermocouple are kept at different temperatures, then a thermo-emf is
produced between the junctions, which changes with temperature difference between the
junctions. Thermo-emf
E = at + bt2
Thermal Equilibrium
When there is no transfer of heat between two bodies in contact, the the bodies are called in
thermal equilibrium.
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If two bodies A and B are separately in thermal equilibrium with thirtli body C, then bodies A
and B will be in thermal equilibrium with each other.
The values of pressure and temperature at which water coexists inequilibrium in all three states
of matter, i.e., ice, water and vapour
called triple point of water.
Specific Heat
The amount of heat required to raise the temperature of unit mass the substance through 1°C is
called its specific heat.
It is denoted by c or s.
The specific heat of water is 4200 J kg-1°C-1 or 1 cal g-1 C-1, which high compared with most
other substances.
Specific heat at constant pressure (Cp) is greater than specific heat constant volume (CV), i.e.,
Cp > CV .
Amount of heat energy required to change the temperature of any substance is given by
Q = mcΔt
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Heat capacity of any body is equal to the amount of heat energy required to increase its
temperature through 1°C.
Heat capacity = me
where c = specific heat of the substance of the body and m = mass of the body.
Water Equivalent
It is the quantity of water whose thermal capacity is same as the heat capacity of the body. It is
denoted by W.
Latent Heat
The heat energy absorbed or released at constant temperature per unit mass for change of state
is called latent heat.
Q = mL
For water at its normal boiling point or condensation temperature (100°C), the latent heat of
vaporisation is
L = 540 cal/g
= 40.8 kJ/ mol
= 2260 kJ/kg
For water at its normal freezing temperature or melting point (0°C), the latent heat of fusion is
L = 80 cal/ g = 60 kJ/mol
= 336 kJ/kg
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It is more painful to get burnt by steam rather than by boiling was 100°C gets converted to
water at 100°C, then it gives out 536 heat. So, it is clear that steam at 100°C has more heat than
wat 100°C (i.e., boiling of water).
After snow falls, the temperature of the atmosphere becomes very This is because the snow
absorbs the heat from the atmosphere to down. So, in the mountains, when snow falls, one does
not feel too but when ice melts, he feels too cold.
There is more shivering effect of ice cream on teeth as compare that of water (obtained from
ice). This is because when ice cream down, it absorbs large amount of heat from teeth.
Melting
Evaporation
Conversion of liquid into vapour at all temperatures (even below boiling point) is called
evaporation.
Boiling
When a liquid is heated gradually, at a particular temperature saturated vapour pressure of the
liquid becomes equal to atmospheric pressure, now bubbles of vapour rise to the surface d
liquid. This process is called boiling of the liquid.
The temperature at which a liquid boils, is called boiling point The boiling point of water
increases with increase in pre sure decreases with decrease in pressure.
Sublimation
Hoar Frost
Calorimetry
This is the branch of heat transfer that deals with the measorette heat. The heat is usually
measured in calories or kilo calories.
Principle of Calorimetry
When a hot body is mixed with a cold body, then heat lost by ha is equal to the heat gained by
cold body.
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Thermal Expansion
Increase in size on heating is called thermal expansion. There are three types of thermal
expansion.
1. Expansion of solids
2. Expansion of liquids
3. Expansion of gases
Expansion of Solids
Increase in length
l2 = l1(1 + α Δt)
where, ll and l2 are initial and final lengths,Δt = change in temperature and α = coefficient of
linear expansion.
α = (Δl/l * Δt)
where, A1 and A2 are initial and final areas and β is a coefficient of superficial expansion.
β = (ΔA/A * Δt)
where V1 and V2 are initial and final volumes and γ is a coefficient of cubical expansion.
2. Expansion of Liquids
(ii) Real Expansion of Liquids When expansion of the container, containing liquid, on heating
is also taken into account, then observed expansion is called real expansion of liquids.
where, yr, and ya are coefficient of real and apparent expansion of liquids and y g is coefficient
of cubical expansion of the container.
When temperature of water is increased from 0°C, then its vol decreases upto 4°C, becomes
minimum at 4°C and then increases. behaviour of water around 4°C is called, anamalous
expansion water.
3. Expansion of Gases
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(i) Volume Coefficient (γv) At constant pressure, the change in volume per unit
volume per degree celsius is called volume coefficient.
where V0, V1, and V2 are volumes of the gas at 0°C, t1°C and t2°C.
(ii) Pressure Coefficient (γp) At constant volume, the change in pressure per unit pressure per
degree celsius is called pressure coefficient.
where p0, p1 and p2 are pressure of the gas at 0°C, t1° C and t2° C.
1. When rails are laid down on the ground, space is left between the end of two rails.
2. The transmission cables are not tightly fixed to the poles.
3. The iron rim to be put on a cart wheel is always of slightly smaller diameter than that of
wheel.
4. A glass stopper jammed in the neck of a glass bottle can be taken out by warming the
neck of the bottles.
Important Points
Due to increment in its time period a pendulum clock becomes slow in summer and will
lose time.
Loss of time in a time period ΔT =(1/2)α ΔθT
∴ Loss of time in any given time interval t can be given by
ΔT =(1/2)α Δθt
At some higher temperature a scale will expand and scale reading will be lesser than true
values, so that
true value = scale reading (1 + α Δt)
Here, Δt is the temperature difference.
However, at lower temperature scale reading will be more or true value will be less.
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The branch of physics which deals with the study of transformation of heat energy into other
forms of energy and vice-versa.
Thermodynamical System
An assembly of an extremely large number of particles whose state can be expressed in terms
of pressure, volume and temperature, is called thermodynamic system.
(i) Open System It exchange both energy and matter with surrounding.
(ii) Closed System It exchanges only energy (not matter) with surroundings.
(iii) Isolated System It exchanges neither energy nor matter with the surrounding.
A thermodynamic system is not always in equilibrium. For example, a gas allowed to expand
freely against vacuum. Similary, a mixture of petrol vapour and air, when ignited by a spark is
not an equilibrium state. Equilibrium is acquired eventually with time.
W = p * ΔV
Work done by a thermodynamic system is equal to the area enclosed between the p-V curve
and the volume axis
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Work done by a thermodynamic system depends not only upon the initial and final states of the
system but also depend upon the path followed in the process.
The total energy possessed by any system due to molecular motion and molecular
configuration, is called its internal energy.
According to this law, two systems in thermal equilibrium with a third system separately are in
thermal equilibrium with each other. Thus, if A and B are separately in equilibrium with C, that
is if TA = TC and TB = TC, then this implies that TA = TB i.e., the systems A and B are also in
thermal equilibrium.
Heat given to a thermodynamic system (ΔQ) is partially utilized in doing work (ΔW) against
the surrounding and the remaining part increases the internal energy (ΔU) of the system.
Therefore, ΔQ = ΔU + ΔW
Therefore, ΔQ = ΔW
Therefore, ΔU = – ΔW
In adiabatic process, if gas expands, its internal energy and hence, temperature decreases and
vice-versa.
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ΔQ = ΔU
Thermodynamic Processes
A thermodynamical process is said to take place when some changes’ occur in the state of a
thermodynamic system i.e., the therrnodynamie parameters of the system change with time.
pV = constant
From first law of thermodynamic dQ = dW, i.e., heat given to the system is equal to the work
done by system surroundings.
where, μ = number of moles, R = ideal gas constant, T = absolute temperature and Vi Vf and Pi,
Pf are initial volumes and pressures.
Examples
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(ii) Adiabatic Process A process taking place in a thermodynamic system for which there is no
exchange of heat between the system and its surroundings.
From dQ = nCdT, Cadi = 0 as dQ = 0, i.e., molar heat capacity for adiabatic process is zero.
From first law, dU = – dW, i.e., work done by the system is equal to decrease in internal
energy. When a system expands adiabatically, work done is positive and hence internal energy
decrease, i.e., the system cools down and vice-versa.
(iii) Isobaric Process A process taking place in a thermodynamic system at constant pressure is
called an isobaric process.
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(iv) Isochoric Process A process taking place in a tlaermodynars system at constant volume is
called an isochoric process.
Volume is constant, so dW = 0,
(v) Cyclic Process When a thermodynamic system returns to . initial state after passing
through several states, then it is called cyclic process.
Efficiency of the cycle is given by
Work done by the cycle can be computed from area enclosed cycle on p- V curve.
The graph drawn between the pressure p and the volume V of a given mass of a gas for an
isothermal process is called isothermal curve and for an adiabatic process it is
called adiabatic curve .
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ES / ET = γ = Cp / CV
where Cp and Cv are specific heats of gas at constant pressure and at constant volume.
c = Δ θ / m Δt = &infi;
c = 0 / m Δt = 0
The second law of thermodynamics gives a fundamental limitation to the efficiency of a heat
engine and the coefficient of performance of a refrigerator. It says that efficiency of a heat
engine can never be unity (or 100%). This implies that heat released to the cold reservoir can
never be made zero.
Kelvin’s Statement
Clausius’ Statement
It is impossible to transfer heat from a lower temperature body to a higher temperature body
without use of an extemal agency.
Planck’s Statement
It is impossible to construct a heat engine that will convert heat completely into work.
All these statements are equivalent as one can be obtained from the other.
Entropy
Entropy is a physical quantity that remains constant during a reversible adiabatic change.
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Heat Engine
A heat energy engine is a device which converts heat energy into mechanical energy.
Q2 is heat rejected to the sink and T1 and T2 are temperatures of source and sink.
(i) External Combustion Engine In this engine fuel is burnt a chamber outside the main body
of the engine. e.g., steam engine. In practical life thermal efficiency of a steam engine varies
from 12% to 16%.
(ii) Internal Combustion Engine In this engine. fuel is burnt inside the main body of the
engine. e.g., petrol and diesel engine. In practical life thermal efficiency of a petrol engine is
26% and a diesel engine is 40%.
Carnot’s Cycle
Carnot devised an ideal cycle of operation for a heat engine, called Carnot’s cycle.
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The net work done per cycle by the engine is numerically equal to the area of the loop
representing the Carnot’s cycle .
After doing the calculations for different processes we can show that
[Efficiency of Carnot engine is maximum (not 1000/0) for given temperatures T1 and T2. But
still Carnot engine is not a practical
engine because many ideal situations have been assumed while designing this engine which
can practically not be obtained.]
A refrigerator or heat pump is a device used for cooling things. It absorb heat from sink at
lower temperature and reject a larger amount of heat to source at higher temperature.
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where Q2 is heat absorbed from the sink, Q1 is heat rejected to source and T1 and T2 are
temperatures of source and sink.
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genius Physics……..Pradeep Kshetrapal Electrostatics 2011
ELECTROSTATICS : Study of Electricity in which Electrostatic series :If two substances are
electric charges are static i.e. not moving, is rubbed together the former in series acquires
called electrostatics the positive charge and later, the –ve.
• STATIC CLING (i) Glass (ii) Flannel (iii) Wool (iv) Silk (v) Hard Metal (vi)
• An electrical phenomenon that accompanies Hard rubber (vii) Sealing wax (viii) Resin (ix) Sulphur
dry weather, causes these pieces of papers to
stick to one another and to the plastic comb. Electron theory of Electrification
• Due to this reason our clothes stick to our
body. • Nucleus of atom is positively charged.
• The electron revolving around it is negatively
• ELECTRIC CHARGE : Electric charge is charged.
characteristic developed in particle of material • They are equal in numbers, hence atom is
due to which it exert force on other such electrically neutral.
particles. It automatically accompanies the • With friction there is transfer of electrons,
particle wherever it goes. hence net charge is developed in the particles.
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• But because free quarks do not exist and their directly proportional to the product of the charges,
sum is always an integral number, it does not inversely proportional to the square of the distance
violet the quantization rules.) between them and
acts along the straight line joining the two charges.
•
Conservation of Charges
•
Like conservation of energy, and Momentum,
the electric charges also follow the rules of
conservation.
1. Isolated (Individual) Electric charge can neither
be created nor destroyed, it can only be
transferred.
2. Charges in pair can be created or destroyed.
Example for 1.
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e0 is permittivity of free space or vacuum and its value • No, In S.I. System, the fundamental quantity is
is e0 = 8.85 x 10-12 coul2 / N x m2 Electric current and its unit is Ampere.
If point charges are immersed in a dielectric medium, Therefore coulomb is defined in it’s terms as
then e0 is replaced by e a quantity-characteristic of the under:
matter involved In such case. For vacuum e = e0 • Coulomb is that quantity of charge which
passes across any section of a conductor per
second when current of one ampere flows
through it, i.e.
• 1 coulomb=1 Ampere x 1 sec
Permittivity, Relative Permittivity and Dielectric
Constant
In cgs electrostatic system, the unit of charge is
Permittivity is a measure of the property of the
called as STATECOULUMB or esu of charge.
medium surrounding electric charge which determine
• In this system electrostatic constant c=1 for
the forces between the charges.
Its value is known as Absolute permittivity of that
Medium e vacuum or air,
More is Permittivity of medium, Less is coulombs One stat coulomb is defined that amount of charge
Force. which when placed at a distance of 1 cm in air from an
For water, permittivity is 80 times then that of vacuum, equal and similar charge repel it with a force of one
hence force between two charges in water will be 1/80 dyne.
time force in vacuum (or air.)
Relative Permittivity(er) : It is a dimension-less In cgs electromagnetic system, the unit of charge is
characteristic constant, which express absolute called ABCOULOMB or emu of charge
permittivity of a medium w.r.t. permittivity of vacuum 1 Coulomb = 3 x 109 statcoulomb
or air. It is also called = 1/10 abcoulomb
Dielectric constant (K) K= er = e/e0 \ 1 emu = 3x1010 esu of charge
q1 12 q2
• Unit of charge:- In S.I. System of units, the 12 21
position vectors be (OA) and (OB). Then If a number of Forces F11, F12,F13,……F1n are acting on a single
AB= . According to triangle law of vectors : charge q1 then charge will experience force F1 equal to
+ = = - and vector sum of all these forces .
= - F1 = F11 + F12 + F13 + …… + F1n
X
(ii) According to Coulumb’s law, the Force 12 exerted on q1
by q2 is given by : 12 = 21 where 21 is a unit
9
Ans : Fe= = 9x10 Newton
-11
Fg=G =6.67x10 Newton
Fe / Fg = 2.26 x 1039
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q X 2q
Bearing
h W h
Q Q
+q a -q (b) If one of the Cs+ ion is missing the crystal is said to have defect.
How much will be the force on chlorine ion in that case?
: if intensity of electric field at a location is E and a 2- Areal distribution: charge is evenly distributed
charge ‘q’ is placed ,then force experienced by this over a surface area,S.
charges F is
The surface charge density is ‘σ‘
given by
Direction of force F is in direction of electric field E Where Q is charge given to a surface of area ‘S’.
DISTRIBUTION OF CHARGE
Electric charge on a body may be concentrated at a
point, then it is called a ‘point charge’. If it is
distributed all over, then it is called distribution of
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E DUE TO +q
ALONG
OPPOSITE TO
NET ELECTRIC FIELD
DIPOLE
2-CO2 & CH4 are non-polar because centers of –ve & SINCE >
+ve charges co-incide and there is no distance between
them.
: IS IN THE DIRECTION OF
3-if non polar atom is placed in an elect.field a distance
is created between +ve & -ve charge: it become polar. IF R>>L THE, E=
E due to +q , E+q
E due to -q E-q
Where ‘q’ is each charge and ‘2L’ is distance between
them.(each charge is at a distance L from ‘center’ of |E+q| = |E-q| = Eq
dipole)
each Eq is resolved in two direction. One along
Dipole moment = q x 2 is a vector quantity it has
magnitude p=2qL equatorial line and other in axial directions which are
And its direction is along line from –q to +q. the Esinθ and normal direction E cosθ .
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E(net) = 2Ecosθ
E= 3/2
IF R>>L Then, E=
------------------------------------------------------------------------
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+q A F
2L
F θ
Field Lines due to some charge configurations.
1.Single positive or negative charge -q B C
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or τ =P x E Or, W = PE – = pE
NOTE :
3.If a dipole is rotated through 900 from the direction
1.Direction of torque is normal to the plane containing of the field, then work done will be
dipole moment P and electric field E and is governed
by right hand screw rule. W = pE = pE
2. If Dipole is parallel to E the torque is Zero. 4. If the dipole is rotated through 1800 from the
direction of the field, then work done will be :
3. Torque is maximum when Dipole is perpendicular to
E and that torque is PE
W = pE = 2 pE
4. This equation gives the definition of dipole moment.
If E is 1 N/C then P=T.
Potential Energy of a dipole kept in Electric field :
Therefore; Dipole Moment of a dipole is equal to the 1. dipole in Equilibrium ( P along E ):-
Torque experience by that dipole when placed in an A dipole is kept in Electric field in equilibrium
electric field of strength 1 N/C at right angle to it. condition, dipole moment P is along E
To calculate Potential Energy of dipole we calculate
5. If a dipole experiencing a torque in electric field is
work done in bringing +q from zero potential i.e. to
allowed to rotate, then it will rotate to align itself to
location B, and add to the work done in bringing –q
the Electric field. But when it reach along the direction
from to position A.
of E the torque become zero. But due to inertia it
1.The work done on –q from up to A
overshoots this equilibrium condition and then starts
= -(Work done up to B + Work done from B to A)
oscillating about this mean position.
2.Work done on +q = +(Work done up to B)
6.Dipole in Non-Uniform Electric field : Adding the two
Total work done = Work done on –q from B to A
In case Electric field is non-uniform, magnitude of force = Force x displacement
on +q and –q will be different, hence a net force will be = -qE x 2L = - 2qLE
acting on centre of mass of dipole and it will make a =- P.E
linear motion. At the same time due to couple of This work done convert into Potential Energy of dipole
forces acting, a torque will also be acting on it. U= -P. E
Work done in rotating a dipole in a uniform Electric If P and E are inclined at angle θ to each other then
field: magnitude of this Potential Energy is
U = - P E Cos θ
1.If a dipole is placed in a uniform electric field
experience a torque. If it is rotated from its equilibrium
position, work has to be done on it. If an Electric dipole
with moment P is placed in electric field E making an
angle α, then torque acting on it at that instant is
Electric – Potential
τ = PESinα
2. If it is rotated further by a small angle dα then work (1) Electric Potential is characteristic of a
done dw = (PEsinα).dα location in the electric field. If a unit
Then work done for rotating it through an angle θ from charge is placed at that location it has
equilibrium position of angle 0 is :- potential energy (due to work done on
its placement at that location). This
potential energy or work done on unit
θ
W= = PE charge in bringing it from infinity is
called potential at that point.
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Energy with Q at B is q VB = -
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VA VB +q -q
2L
VA > vB
Q
This also show that an electric charge At P – V+q =
4 0 ( r l )
experience force from high potential towards
low potential if allowed to move, it will do so in Q
this direction only. V-q =
4 0 ( r l )
If E and are not collinear and make angle
between them, then according to relation of 1 1
Total V =– V+q + V-q =
work & force r l r l
dv = - E dr Cos
Or, - dv / dr = E Cos =
2Ql
=
P
Or, dv = - E . dr 4 0 ( r l )
2 2
4 0 (r 2 l 2 )
Or V = E . dr P
If r > > L Then V =
4 0 r 2
( work) given by dot product of two vector - q & + q are placed at A & B. Point P is on equatorial
E & dr.
V = V1 + V2 + V3
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Q r L cos r LCos
=
4 0 r 2 L2Cos 2
Q X 2 LCos
=
4 0 (r 2 L2Cos )
PCos v
Then, Or, V =
4 0 r 2
0,0 R r
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V+v ’
V2
v’ V
V1
Gauss's Law
Electric Flux
Think of air blowing in through a window. How much
air comes through the window depends upon the speed
of the air, the direction of the air, and the area of the
Proof:- Suppose E is window. We might call this air that comes through the
not at right angle to equipotential surface, and makes window the "air flux".
angle with it. Then it has two components, E Cos
along surface and E Sin normal to surface due to We will define the electric flux for an electric field
that is perpendicular to an area as
component E Cos , force q E Cos should be
created on surface and it should move the charge. But =EA
we find that charges are in equilibrium. i.e.
E Cos = 0 ;
since E = 0, therefore Cos = 0 or ∠ = 900
Hence E is always at right angle to equip. surface.
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For a curved surface, that will not be the case. For that
case, we can apply this definition of the electric flux
over a small area A or A or An.
=E A cos or
=E A
=E A
A=An
Gauss’s Law : Total electric flux though a closed
where n is a unit vector pointing perpendicular to the surface is 1/ε₀ times the charge enclosed in the
area. In that case, we could also write the electric flux surface.
across an area as
ΦE=q / ε₀
=E nA But we know that Electrical flux through a closed
surface is
Both forms say the same thing. For this to make any
sense, we must be talking about an area where the
= q / ε₀
direction of A or n is constant.
This is Gauss’s theorem.
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PROOF : Let’s consider an hypothetical spherical Consider a Gaussian Surface in the shape of a cylinder
surface having charge q placed at its centre. At every having axis along conductor. It has radius r so that
point of sphere the electrical field is radial, hence point P lies on the surface. Let its length be l.
making angle 0 degree with area vector. The electric field is normal to conductor, hence it is
symmetrical to the surfaces of these cylinder.
Electric field due to line charge : Let’s consider a Gaussian surface, in shape of a cylinder
Electric charge is distributed on an infinite long straight which has axis normal to the sheet of charge and
conductor with linear charge density λ. We have to containing point P at its plain surface (radius a ).
find Electric field on a point P at normal distance r.
Electric field E is normal to the surface containing
charge hence it is normal to the plain surface of
cylinder and parallel to curved surface.
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Or E=
Now = for curved surface + for 2
plane surfaces.
= + + This expression is same as electric field due to a point
= for plain surfaces 2E ( E is uniform) charge q placed at distance r from P. i.e. In this case if
= 2Eπa2 complete charge q is placed at the centre of shell the
The charge enclosed inside Gaussian surface q = σ.A electric field is same.
Or, q = σπa2
Case 2. If P is on the surface.
Applying Gauss’s Law : = q / ε₀ In above formula when r decrease to R the electric
field increase.
Putting values 2Eπa2 =
On the surface (replace r with R) E=
Or E= Hence this is electric field on the surface of a shell and
its value is maximum compared to any other point.
Electric Field due to charge distributed over a
spherical shell :- Case 3. If P is within the surface. Or ‘r’ R
Charged Shell +
+ +
+ +
+ R +
+
r +
+ + + Gaussian Surface
+ +
+ +
+ + + +
+ R + + +
+ +
r Let’s consider +a Gaussian surface, a concentric
+ + P E spherical shell of radius r passing through P.
+ +
+ +
+ + Then charge contained inside Gaussian surface is Zero.
+
According to Gauss’s Theorem = q / ε₀
If q is zero then = 0.
As ds is not zero then E = 0
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Gaussian Surface E
Charged Sphere
+++++++++
++++++++
++ + + + + + + +
r
+++++++++ R
E
+ + + + + + + +P +
+ + + + + +++ + +
+++++++++
+++++++++
++ + + + + + + +
+++++++++ Electric field due to two charged parallel surface
Charges of similar nature
+++++++++
1 2
+++++++++
E1 = - + E1 = + + E1 = +
+ +++ + + + + + +
+ +
+++++++++ + +
+++++++++ E2 = - + E2 = - E2 = +
+
+++++++++ + +
Case I. When+P+is+ Out
+ + +side
+ + sphere.
+ Same as in the case + +
+ + + + + + + + + E=E1+E2= - + E=0 E=E1+E2= +
of charged shell E = +
+++++++++ + +
a. Charges of + opposite nature + :-
Case 2. When + +point
+ + +P+ is+ +on+ the surface of shell: Same
+1 2+
+++++++++ +
as in case of shell . E = ++ E1 = + + E =+
+++++++++ E1 = - -+ 1
Case 3 If point++P + +is+inside
+ + + +the charged sphere. ++
-+
Consider Gaussian surface, a concentric spherical shell +
++++++++ E2 = + -
of radius r, such that point P lies on the surface. + E2 = + E2 = -
Electric field is normal to the surface. + -
+ -
E= -E1 + E2= 0 E=+E1+E2 E= +E1 - E2= 0
Now = for complete area of Gaussian surface + -
+ =+ -
= = E (E is uniform)
+ -
= E x 4πr . (for spherical shell
2
= 4πr2 )
+
-
+ :
Equipotential Surface
Charge within Gaussian surface = charge density x -
+
volume. Energyof a charged + particle in terms - of potential:-
= ρ πr3 (where ρ is the charge per unit volume.) -
Applying Gauss’s Law = q / ε₀
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Electron-Volt : By relation Work/energy = qV, the Corona discharge : when an uncharged body is
smallest unit of work/energy is Electron Volt. brought near a charged body having sharp corners
there is large number of charges at the corners. Due to
One electron volt is the work done by/on one induction, they induce large number of opposite
electron for moving between two points having charges. This creates a very strong Electric field
potential difference of one Volt. between them. Finally the dielectric strength breaks-
down and there is fast flow of charges. This Spray of
1 eV = 1.6 x 10-19 Joules charges by spiked object is called Corona discharge.
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CAPACITOR
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It is a device to store charge and in turn store the PARALLEL PLATE CAPACITOR : -
electrical energy.
Since single conductor capacitor do not have large
Any conductor can store charge to some extent. But capacitance , parallel plate capacitors are
we cannot give infinite charge to a conductor. When constructed.
charge is given to a conductor its potential increases.
But charge cannot escape the conductor because air, Principle : Principle of a parallel plate capacitor is
or medium around conductor is di-electric. that an uncharged plate brought bear a charged
When due to increasing charge the potential increase plate decrease the potential of charged plate and
to such extent that air touching the conductor starts hence its capacitance (C = ) increase. Now it can
getting ionized and hence charge gets leaked. No take more charge. Now if uncharged conductor is
more charge can be stored and no more potential earthed, the potential of charged plate further
increase. This is limit of charging a conductor. decreases and capacitance further increases. This
arrangement of two parallel plates is called parallel
The electric field which can ionize air is 3 x 109 vm-1. plate capacitor.
CAPACITANCE OF A CONDUCTOR Expression for capacitance :
q
Term capacitance of a conductor is the ratio of charge Charge q is given to a plate
to it by rise in its Potential + -
Of area ‘A’. Another plate
C= -
+ -
is kept at a distance ‘d’.
A E
In this relation if V=1 then C= q. Therefore , -
After induction an +
-
Capacitance of a conductor is equal to the charge
Electric field E is set-up + -
which can change its potential by one volt.
-
Unit of capacitance : Unit of capacitance is Between the plates. Here + d -
farad, (symbol F ). q = σA and E= -
+ - by
One farad is capacitance of such a conductor whose The Potential difference between plates is given
potential increase by one volt when charge of one V = Ed = d -
+
coulomb is given to it. -
Now C = = = +
One coulomb is a very large unit. The practical smaller
units are
+
i. Micro farad ( μF ) = 10-6F.(used in electrical circuits) C =
Ii Pieco farad ( pF) = 10-12 used in electronics circuits
+
If a dielectric of dielectric constant K is inserted
Expression for capacitance of a spherical conductor : between the plates, then capacitance increase by
+
If charge q is given to a spherical conductor of radius r, factor K and become
its potential rise by V = +
Therefore capacitance C = = q/ = C =
+
Or for a sphere C= Note : The capacitance depends only on its
configuration i.e. plate area and distance, and on the
The capacitor depends only on the radius or size medium between them.
of the conductor. The other examples of parallel plate capacitors is
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or p = αε₀E₀
= χeεE
E. = E - Ep = =
or ( =σ
or =σ
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