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04 HT Course Material 2020 21 Iisem
04 HT Course Material 2020 21 Iisem
04 HT Course Material 2020 21 Iisem
UNIT-I
The science of thermodynamics deals with the amount of heat transfer as a system
undergoes a process from one equilibrium state to another, and makes no reference to how long
the process will take. But in engineering, we are often interested in the rate of heat transfer,
which is the topic of the science of heat transfer. The study of heat transfer has become an
increasingly intense concern in modern technology. In the fields of refrigeration and air
conditioning, computer hardware, electrical engineering civil engineering, geothermal
engineering and in electronic equipment cooling, chemical technology etc… there is a need to
understand and predict how heat energy is carried, distributed and diffused in and by different
materials. This is possible only if we have knowledge of heat transfer. The study of heat transfer
includes the physical process where thermal energy is transferred as a result of a temperature
difference. There are basically two distinct processes for the transport of heat energy viz.,
Conduction and Radiation. If conduction occurs in a medium where there is a relative motion of
particles it is called Convection. Therefore the study of heat transfer requires the knowledge of
the three modes of heat transfer conduction, convection and radiation.
1.1 CONDUCTION
This is the mode of heat transfer, which occurs in a medium with out any relative motion
of particles, though it is impermeable to any other kind of radiation.
This dependence was established by Fourier’s law of conduction which states that
Q dT A.T
or Q
A dx x
The rate of heat transfer per unit area is directly proportional to the temperature gradient. The
proportionality is removed by a constant denoted by ‘k’ known as Thermal conductivity.
dT T
Q = kA kA (Watts)
dx L
The negative sign is introduced since the heat always flows from higher temperature to lower
temperature i.e., opposite to the temperature gradient. The above equation is called Fourier rate
equation.
The value kA/L is known as “conductance” of the plate. And Q /A is known as Heat flux denoted
by ‘q’. From above equation it follows that the rate of heat flow will be the rate along the lines
normal to isothermal surface. If this flow of heat is considered in different directions x,y,z in a
solid we have
dT dT dT
q x -k x , q y -k y and q z -k z
dx dy dz
Where Kx, Kyand Kz represent thermal conductivities in x,y,z directions.
Thermal conductivity is a physical parameter of the substance indicating the substance
capacity to conduct heat.
Q. x
From Fourier equation k =
A. T
When x =1, A= 1, T= 1 unit, k = Q. so we can define the thermal conductivity of a substance
as the quantity of heat it can transfer by conduction per unit area of the isothermal surface per
unit time at a unit temperature gradient. Higher the value of k higher the substance ability to
conduct heat. In general k depends on temperature, pressure and nature of the substance and is
determined experimentally.
1.2 CONVECTION
This is delivered from the latin word ‘convehere’ means bring in or to carry. This is the mode
of heat transfer, which occurs due to the motion of molecules carrying heat from one zone to
another zone. For example if we keep a hot cup of coffee in a stream of air, it gets cooled and we
say heat is convected away by air. The molecules of air while moving over the hot coffee surface
pickup heat and release in a low temperature zone. When we pour the coffee in saucer and
expose it to the same stream of air it gets cooled more quickly because the exposed surface area
of hot fluid increases. Thus convective heat transfer is directly proportional to the exposed
surface area and it is also proportional to the temperature difference between the surface and
stream.
Q A.T
This is known as Newton’s law of
cooling, which states that the rate of heat
transfer by convection is proportional to
exposed surface area and temperature
difference.
If the proportionality is removed we have to
introduce a constant ‘h’ known as convective
heat transfer coefficient.
Q h. As.T h. As.Ts T Watts
Q
h W / m2 K
AS .T
1.3 Radiation:
Radiation is an electromagnetic phenomenon in which heat energy is carried by the
waves in quantum. This can happen between bodies without any presence of medium as earth
receiving heat from sun through space. For conduction and convection to transfer heat we need
temperature difference (driving potential which cause heat flow from high temperature to low
temperature) where as in radiation when ever a body is at a temperature greater than 0 K .i.e., -
273 0C it experience molecular motion vibration & collision which result in emitting energy at
various wave lengths. This heat emitted by a body through electromagnetic waves is known as
radiation. Thus all objects will continue to emit radiant heat energy in all directions when their
temperature is above 0K and is governed by Stefan Boltzman law. It states that the amount of
heat energy emitted by a black body is directly proportional to fourth power of its absolute
temperature.
Q b AT 4
or Q b AT 4 Watts
is called Stefan Boltzman constant and is given as 5.67 10 8 W/m 2 K 4
Black body is an ideal body, which is a perfect emitter and perfect absorber. Real body
surfaces are not ideal and they emit less energy than a black body. The ratio of energy emitted by
a real body to that of a black body is known as emissivity denoted by .
E E
real real4
Eblack T
Qreal AT 4 Watts
If a black body at temperature T1 having area A1 is completely surrounded by an environment
(black body) at temperature T2 then the net Heat Exchange between them is given by
Qb12 A1 T14 T24 watts.
Since the value of is very low, radiation heat is dominant only when the bodies are at
high temperature. More detailed discussion on radiation is presented in chapter on Radiation.
T
Q x - k x . y.z - (2.1)
x
T
Q y - k y . x.z
y
T
Q z - k z . y.x
z
Further the heat leaving in x direction at x + x is mathematically expressed as
Q x Δ x Q x Q x .x
x
Similarly in y and z directions
Q y y Q y Q y .y
y
Q z z Q z Q z .z
z
The amount of total heat generated in the elemental volume = qG vol
= qG x y z
If we assume the density of the element ρ then the mass of the element m x.y .z
The energy accumulated is responsible for increasing the internal heat capacity of the
T
element given by m.C. Where ‘C’ is the specific heat of the material in J/kg k and ‘t’
t
represents time.
T
Q x Q y Q z qG .x.y.z Q x dx Q y dy Q z dz m.C.
t
Substituting equations 2.4, 2.5, 2.6 in (2.9) we get
T
Qx x Q y y Qz z qG .x.y.z m . C .
x y z t
Substituting 2.1, 2.3 and 2.7 and treating ‘k’ as independent of Temp
2T 2T 2T T
k x x.y.z 2 k y x.y.z 2 k z x.y.z 2 qG x.y.z ρ .x.y.z.C .
x y z t
2T 2T 2T T
kx k k qG ρ .C
x y z t
2 y 2 z 2
2T 2T 2T qG ρ .C T
.
x 2 y 2 z 2 k k t
k
Where is known as thermal diffusivity in units m2/s.
ρ .C
Thermal diffusivity is a property of the material and indicates the rate at which the heat
energy is distributed in a material. Higher the ‘k’ value of material the faster is the ‘spreading’ of
heat energy and equalization of temperature through out the substance is faster. A value of c i.e.
heat storage capacity represent sluggish nature of distribution of heat. Metals have large
diffusivity compared to non-metals. Liquids exhibit a very small diffusivity. Gasses have high
value of thermal diffusivity and hence metals and gases respond quickly to temperature changes
in the surroundings when compared to non-metals and liquids.
T
Now Qr dr k .rdθ .r sin d .dr.
r r r
2 T
k .dθ . sin d r .dr.
r r
2 T
= k.d.dr. sin d r
r r
Q rd k .dr.r sin d T .r d.
r r r
T
k .dr.d.d sin
Q .r sin .d k .dr .rd. sin T d r sin d.
r sin r sin r sin
k .dr .d.d T
sin
Substituting these in the above equations
2 T T dr .d.d T
k .dr .dθ .d sin r k .dr .d.d sin k . qG . dr . dθ .d.r 2 sin
r r sin
T
ρ . dr . rdθ .r sin .d.C .
t
dividing the above equation with k .r 2 . sin . dr . dθ .d we get
1 r 2 T .dr 1 T 1 T q G C T
sin 2
r 2 r r r sin
2
r sin
2
k k t
1 2 T 1 T 1 T qG 1 T
.dr 2 sin 2 .
r sin k
r
r r r
2
r sin 2
t
1 2 T
. r 0
r 2 r r
2T 2T 2T qG 1 T
.
x 2 y 2 z 2 k t
qG 1 T
or 2T . where is Laplace operator.
k t
When the temperature is not varying w.r.t time i.e. under steady state condition the above
equation reduces to
2T 2T 2T q G
+ + + =0
x 2 y 2 z 2 k
T
=0
t
q
Or 2T G and is known as Poisson’s equation.
k
Finally for one dimensional, steady state without heat generation it reduces to
2T
0
x 2
T
If k is treated as a function of temperature we get k x = 0
x
Solution of these equations subject to the boundary conditions will yield the temperature
distribution in the solid. Then by using Fourier law we can find the heat transfer in any direction.
1.9. Initial and Boundary Conditions
The conditions are specified at the surface x =0 for a one-dimensional system. Heat
transfer is in the positive x direction with the temperature distribution, which may be time
dependent, designated as T( x, t ) . The first condition corresponds to a situation for which the
surface is maintained at a fixed temperature Ts. It is commonly termed a Dirichlet condition, or a
boundary condition of the first kind. It is closely approximated, for example, when the surface is
in contact with a melting solid or a boiling liquid. In both cases there is heat transfer at the
surface, while the surface remains at the temperature of the phase change process. The second
condition corresponds to the existence of a fixed or constant heat flux at the surface. This
heat flux is related to the temperature gradient at the surface by Fourier's Law, which may be
expressed as
It is termed as Neumann condition, or a boundary condition of the second kind, and may be
realized by bonding a thin film or patch electric heater to the surface. A special case of this
condition corresponds to the perfectly insulated, or adiabatic, surface for which. The boundary
condition of the third kind corresponds to the existence of convection heating (or cooling) at the
surface and is obtained from the surface energy balance.
HEAT TRANSFER COURSE MATERIAL (A36C2)
UNIT-II
2T T
0 C1
x 2 x
T C1x C2
T2 T1
T1 C2 and C1
L
T T1
Substituting we get T 2 x T1
L
Consider an elemental ring of ‘ dr ’ thickness at radius r from the center. The area of the
strip perpendicular to the direction of heat flow is 2πr L and dr is so small that r dr r .
Now applying Fourier law.
dT
Q kA. where A 2πr.L and dx dr
dx
dT
Q k .2πrL
dr
Temperature distribution in a hollow cylinder
T
The one dimensional conduction equation in cylindrical coordinates is r 0
r r
T T C 1
On integration r C 1
r r r
Again integrating we get T C1 ln r C2 .
The solution of this can be obtained by specifying boundary conditions as
At r ri , T Ti and at r ro , T To as substitution
C1
Ti To Ti ln ro To ln ri
and C 2
ri r
ln ln o
ro ri
Hence the temperature distribution in a hallow cylinder is logarithmic in nature
r r
Ti ln To ln i
ro r
T
r
ln i
ro
V
I . Temperature difference is analogous to voltage difference across the conductor and
R
resistance of the conductor is analogous to conduction resistance of the slab. Fig. explains the
similarities between heat flow and current flow.
T
Q Where RCond through slab L
R
Cond
kA
T
Q
1 r 1
ln 2
2kL r1 ho .2r2 L
dQ T 1 1 1 1
0 2
d r2 1 r2 1 2kL r2 2Lho r2
2
ln
2kL r1 ho .2r2 L
1 1
2kLr2 2Lho r2 2
k
r2 . This radius is known as critical radius.
ho
k
rC
ho
Using electrical analogy and résistance method we can also derive the same expression.
The three layers offer resistance to flow of heat in series as shown in figure given below.
k 0 1 α.T . A.
dT dT
Q kA
dx dx
q k 0 1 α.T .
dT
dx
qdx k 0 1 α.T .dT
Integrating on both sides
2
k m . A.T2 T1
Q 1 C.F
L
T1 T2
Where CF is the correction factor and is equal to . .
2
2.10. Conduction with Internal Heat Generation
In many circumstances generation or absorption of heat takes place within the body itself
e.g. in electrical heating appliances, nuclear reactors, chemical beds, drying and setting of
concrete and in electrical cables etc… Electric current flowing in a conductor results in heat
generation due to electrical resistance. Induction heating introduces the energy into the material
in a distributed way. Chemical reaction may occur in a material and result in either positive or
negative heat transfer. In nuclear reactor fuel elements, moderators, shielding etc… there is heat
generation due to the deceleration and absorption of neutrons or due to absorption of gamma
radiation etc.
dT
The boundary conditions are (Ref to the fig) at x = 0, T T max i.e. = 0.i.e. the max
dx
temperature in the slab occurs at the surface of insulation due to accumulation of heat at the point.
qL2
The other boundary condition is at x = L, T = Ts applying these we get C1 = 0, C2 =
2k
T max .
.
q x 2 qL2
T
2k 2k
This is the temperature distribution equation in the slab.
dT
If we use Q = k A we will get Q = at the insulated surface.
dx x 0
.
q ro2 ri 2
Ti To + C1 ln ri ln ro
4k
.
q 2
(Ti - T0 ) [r0 ri ]
2
2
4 k qr1
C1 and C 2 Ti C1 ln ri
ln( r0 ri ) 4k
Substituting these we get the Temp distribution.
If we consider a solid cylinder of radius ‘r’ with its surface temperature maintained at T w and
subjected to a convective environment with ‘h’ at T then the boundary conditions are
at r r0 , T Tw
dT
at r 0, T Tmax i.e 0
dr
Substituting these in the temperature distribution equation
dT qr C
1 0 at r 0 C1 0
dr 2k r
2
qr
Tw 0 C 2 C 2 0
4k
.
q(r02 r 2 )
Hence T TW
4k
.
qr02
Tmax is at r = 0 Tmax Tw
4k
The value of Tw can be obtained by using energy balance equation
.
qr0
Tw T
2h
. .
q(r0 r 2 )
qr0
T T
2h 4k
. .
qr 2
qr0
and Tmax T 0 ……
2h 4k
T1 C2
6k ri
qr0 C1
2
T
.
qr q r0 r 2
2 2 2
qr
Hence T 0 Tw Or T w
6k 6k 6k
2
qr
The maximum temp will be at the center i.e. at r = 0 Hence Tmax 0 Tw
6k
To obtain the TW we can use the following energy balance equation.
Heat generated in the sphere = Heat lost to the environment by convection
q r0 h.4.r0 Tw T
4 3 2
qr0
Tw T
3h
q [r0 r 2 ]
2
qr0
T T
3h 6k
2
qr0 qr0
And TMax at r = 0, is Tmax T
3h 6k
The fins are classified as uniform and non-uniform cross section area fins. Analysis of
uniform area fins is relatively easy and is taken up first in this chapter.
2
m2 0
x 2
This is the general differential equation for a fin. The assumptions used for this are
1) Steady state 2) No heat generation 3) K value is constant 4) h is also constant 5)
Area of cross section is uniform and hence perimeter.
represents the excess temperature at any location all along the length of the fin. The
solution of the above 2nd order linear homogeneous differential equation is.
θ C1 e m x C 2 e m x
Where C1, C2 are arbitrary constants whose values are to be determined from the
specified boundary conditions. We need at least two conditions to find C1, C2. From this
dθ
equation we can find using kA / x 0 at x = 0. Because the heat transfer is purely by
dx
conduction at the base.
From the above equation it is evident that temperature distribution is non-linear and is
totally governed by the fin configuration. Solution to the above equation is obtained by
considering three different cases as follows.
kA 0 e m x m
x 0 mkA0
Q h A T where A Pdx, T
L
Q h p dx
0
e mx hP 0
hP 0 e mx
.dx hP 0 0 1
0 m 0 m
Q hPkA. 0
Under steady state the rate of heat transfer entering into the fin by conduction is equal to
the amount leaving from its surface by convection. In general no fin is of infinite length and the
above equations give reasonable accurate temperature and heat transfer values if the length of the
fin is very large compared to its cross sectional area.
2.11.3. Heat transfer from fin with its end insulated (Negligible heat transfer from end)
Infinite long fin analysis is far off from practical consideration since the temperature after
certain length on the fin approaches T and rate of heat transfer by convection beyond that point
is negligibly small. So it is an unnecessary extended portion occupying space, increasing cost
etc.. hence infinite long fins are not likely to be present. A more practical approach is when the
end area of the fin is very small the rate of heat transfer from that area is negligible and thus the
fin tip may be assumed to be insulated. The boundary conditions for this case are:
d d
at x 0, T T0 0 and x L, kA 0 i.e 0
dx dx x L
Substituting in equation we get 0 C1 C2 (1)
0 C1e mL C2 e mL
C1 C 2 e 2mL substituin g this in equation (1)
0 0 e 2m L
C2 and C1
1 e 2m L 1 e 2 m L
0 0
emx 2 m L
e m x
1 e 2m L
1 e
Multiplying 1st term with emL and 2nd term with e-mL both numerator and denominator we get,
e m x em x
0 2 m L 2m L
e 1 e 1
e m( L x ) e m( L x )
0 ( )
e m L e m L
cosh m( L x) T T cosh m( L x)
0 . i.e
cosh mL T0 T cosh mL
The heat transfer from the fin is obtained by
d m.sinh mL x
Q kA kA 0
dx x 0 cosh mL x 0
sinh mL
kAm. o hPkA. o . tanh mL
cosh mL
No fin will be insulated at its end but a triangular fin is an example for this case since the area at
the end is negligibly small.
C1e m L C 2 e m L
h
Km
C1e m L C 2 e m L .
Substituting C 2 θ 0 C1
h m L
0 1 e
km
C1
e m L e m L h mL
km
e e m L
h m L
0 1 e
km
and C2
e m L e m L km
h mL
e e m L
Substituting these in the general equation we get
e
m( L x
e m ( L x
h m( L x
Km
e
e m( L x
θ θ0
h or
e m L e m L (e m L e m L )
Km
h
cosh m ( L x) sinh m ( L x)
0 mk
h
cosh mL sinh m L
mk
tanh m L
fin
mL
If the fin is very long (mL) is very large and fin efficiency will be less. Since tanh m L
value significantly increases only up to a value of mL =3 there after it stands at one. That is the
reason why in most of the fin designs the value of mL is restricted to 2.5. Similarly when L 0
the efficiency of fin tends to 100% i.e. when there is no fin at all the heat transfer rate from that
surface is at base temperature only and efficiency leads to 100%.
So fin efficiency is an indication to what extent the temperature along the length varies
from that of its base temperature. Efficiency is more means the temperature is less and vice
versa. If we know the fin efficiency the actual heat transfer from the fin can be calculated easily
by using
Qact Qideal .h. As .0
Qact h As (T0 T )
Cos h m( L x)
Assuming negligible heat loss from its end
0 Cos h mL
T TG
Where,
0 T0 TG
T0 is the temperature of the pipe wall.
T is temperature at a distance of x
TG is the gas temp.
TL TG cos h m[ L L] 1
At x L
T0 TG cos h mL cos h mL
hP h ( d ) h
and m
kA k.( d .t ) kt
Where TL is the temperature recorded by the thermometer. Using equation, we can find the
gas temperature.
1
There will be no error if 0 . I.e. for higher values of mL the error between
cos h mL
the reading and original gas temperature will be minimum.
Further it is observed from the expression for m and the error is independent of
0
diameter of the tube well.
To increase the value of m we have to use very thin tubes or low k value materials.
To increase the value of L the well may be set up in an inclined position.
HEAT TRANSFER COURSE MATERIAL (A36C2)
UNIT-III
In many practical applications the temperature of a body varies with time as well as
position. All cooling or heating process of a solid material with convection or thermal radiation
at the surface fall under unsteady state conduction In the preceding chapter we have considered
the heat transfer under steady state in which temperature of a body at any point does not change
with time. This chapter is devoted to consider the heat transfer under unsteady state i.e. the
variation of temperature with time as well as position. The change in temperature during
unsteady state may follow a periodic or non-periodic variation. In periodic variation,
temperature changes in a cyclic manner repeating the same changes after some fixed intervals of
time. like in Ic engine cylinder wall, a building roof exposed to sun etc.. In non-periodic
variation the temperature changes are some non-linear function of time, as In heating & cooling
of ingots, bars, billets etc..
Thus the unsteady state problems can be broadly divided into four categories a) lumped
system or infinite conductivity b) finite conductivity and convective resistance c) semi infinite
thick solids d) periodic variation. The unsteady state heat transfer under above conditions is
explained in the foregoing sessions.
The one dimensional conduction equation under unsteady state condition is given by
2 T 1 T
.
x 2 t
Solution of the above equation subjected to the specified boundary conditions will lead to
the temperature distribution in a solid as a function of x & t. T = f (x,t) Analytical solution of the
above equation can be obtained using variable separable method. Use of graphs and tables to
obtain the solution for complicated systems is also explained in this chapter.
ln T T 0 C1 . Substituting we get
T T hAt
ln
T0 T vC
hAt
T T
e vC
T0 T
hAt
e vC
0
Where,
is temperature difference at any instant, t sec
0 is temperature difference initially at t = 0 sec
This is the equation for variation of body temperature in a lumped system. Note that it is
a function of ‘t’ only and is independent of x. This can be also expressed as
hAt hv kA2
t
vC kA v 2 C
hAt hv kA2
t
vC kA v 2 C
hLc t k V
2 Where Thermal diffusivity , characteristic length Lc .
k Lc C A
Bi , Fo
e Bi, Fo
0
Where Bi represents Biot Number which is the ratio of internal conduction resistance to that
external convective resistance. Fo represents Fourier number and is defined as
Rate of heat conduction in the body t
Fo
Rate of heat storage in the same body L 2
c
Thus Fourier number represents the measure of rate of heat conduction in comparison
with the rate of heat storage in a given volume element. Higher is the value, deeper the
penetration of heat into a solid over a given time.
Lc is the characteristic length, which is the ratio of volume to surface area. For different
geometries the Lc valve is calculated as follows:
4 R 3
R
for a sphere Lc 3 2
4R 3
L3 L
for a cube Lc 2
6L 6
R 2 L R
for a cylinder Lc
2RL 2
3.2.1. Time constant:
hAt
T T
In the equation e ρvC if we make
T0 T
hAt vC vC
1 by taking t , the value of is called time constant and is
vC hA hA
denoted by t*.
vC
t* .
hA
hA
If the time taken for cooling is t = t*, then .t will be equal to one and
vC
T T
e 1 0.3678
T0 T
If the time taken for cooling is t = 2 t* i.e two time constants then
T T
e 2 0.1353
T0 T
So one time constant is defined as the time required for the temperature of the body to
reach 63.2% of its initial temperature difference. The time taken by a thermocouple to reach the
surface temperature is defined as response time. Lower the value of time constant, better the
response of a system. Generally the time constant lies between 0.04 to 2.5 sec.
The sensitivity of the thermocouple is defined as the time required by the thermocouple
to reach 63.2 % of the value of the initial temperature difference.
Thus For practical purpose, the reading of a thermocouple should be taken after a period
equal to 4 time constants have elapsed. (4t*).
hAt
For better response must be large i.e. by decreasing the wire diameter, or
vC
minimizing the volume to area ratio we can achieve it. Thus the shape of thermocouple head
should be spherical to have maximum response.
The above analysis assumes uniform distribution of temperature throughout the body i.e.
where the body offers no internal resistance for conduction or the body is having infinite thermal
conductivity. Therefore this system is applicable only when Bi = 0.
However in reality nobody will have infinite thermal conductivity or negligible
conduction resistance. But in the case of a spherical steel ball of small diameter, or a thin copper
electrical conducting wire, because of their good conducting nature, the difference in temperature
between surface and at center is negligible and hence can be treated as a lumped system. Hence
though there is no system with infinite k value, bodies having very low characteristic dimension
like thin wires or having high k value like Cu, Ag spheres& wires will fall under this category.
We approximate that the case is applicable when Bi 0.1
3.3. Systems with finite conduction and convective resistances:
Consider a plane wall of thickness 2L extending
to infinity in the Y and Z directions. Let us assume that
the wall is initially at a uniform temperature T0 and is
suddenly exposed to atmosphere, which is at a
temperature Ta having heat transfer coefficient ‘h’
2T 1 T
The governing equation for this is .
x 2 t
the boundary conditions are t 0,
T T0 for L x L
T
0 at x 0
x
T
k hT T at x L
x
assuming T T
2
2
t x
0 at t 0, and 0 at x 0
x
h
at x L for t 0 .
x k
The solution of the above equation is
C1 cos x C 2 sin x .e t
2
The Heisler Charts are used to solve the problems with finite conduction and convection
resistance.
HEAT TRANSFER COURSE MATERIAL (A36C2)
UNIT-IV
u
τμ
y
where τ =shear stress [N/m2]
μ = Absolute viscosity [kg/ms]
u
= Rate of shear deformation [1/s]
y
In the case of non-Newtonian fluids equation is non-linear and it is represented by the non-linear
relationship as
n
u
τ m
y
If n is different from unity the fluid is known as non-Newtonian and such fluids are
termed as power law fluids. Fluids following above equation are known as Ostwald-de-Waele
fluids.
respectively by u, v, w in x,y,z directions. The element under consideration must obey the law of
continuity. With reference to the fluid element the conservation of mass states that the net rate of
in flow into the control volume is equal to accumulation rate of the control volume. Thus,
x m
[m y m
z ] [m
x x m
yy m
zz ] M
where
:
x ρuyz : m
m z ρwxy
y ρvxz m
x x = ρuyz
m
ρuyzx : m y y = ρvxz ρvxzy
x y
m z z = ρwxy ρwxyz
z
net rate of accumlatio n in the controlvol ume [ρxyz]
M τ
ρ
[ρu ] [ρv] [ρw ] 0
τ x y z
For incompressible medium density variation with respect to position or time can be ignored i.e.,
ρ
=0 and thus, the law of continuity is as follows for a two-dimensional flow
τ
u v
0
x y
u u u P τ x
ρ u v ρg x
τ x y x y
Proceeding along similar lines the equation of motion in y-direction can be written as follows.
v v v P τ y
ρ u v ρg y
τ x y y x
The shear force terms for Newtonian fluids can be further expressed for two-dimensional motion
as follows.
τ x 2u 2u
μ 2 2
x x y
τ y 2v 2v
μ 2 2
y x y
Thus, the equations of motions in x and y directions are listed as follows.
in x
u u P 2u 2u
ρ u v μ 2 2 ρg x
x y x x y
in y
v v P 2v 2v
ρ u v μ 2 2 ρg y
x y y x y
However, for flow over a horizontal plate gx= 0
T 2T 2T 2T
ρCp k 2 2 2
τ x y z
T
The partial derivative ρCp should be treated as a substantiative derivative written as
τ
DT
ρC p . . The substantiative derivative for a moving medium can be written as follows
dτ
DT T dx T dy T dZ T
ρCp ρCp
dτ x dτ y dτ z dτ τ
dx dy dz
However, u ;v ;w where u, v, z are respectively velocities in x, y, z directions of
dτ dτ dτ
the coordinate system.
Thus, the energy equation in its general form can be written as follows
T T T T 2T 2T 2T
ρCpu v w
z τ
k 2 2 2
x y x y z
Thus, for two-dimensional motion of the fluid in x, y directions can be written as follows for
steady state conditions
T T 2T 2T T
C p u v k 2 2 0
x y x y τ
h ρ Cp
1= : π 2 b1 b 2 b3 b 4 : π 3 c1 c 2
D k V μ
a1 a3 a4
a2
D k V μ D k V c3
μ c4
Substitution of dimensions from the table for respective parameters will yield the following
M 1 1 T 3 2 T 3 LT
a a a a4
[ 1 ] 3
T L ML L M
M 1 1 T 3 T 3 LT
b b2 b b4
[ 2 ] 3
L L ML L M
C4
L2 1 1 T 3
C C2 C3
[ 3 ] 2 T LT
T L ML L M
M L T
1 1-a2-a4=0 -a1-a2-a3+a4=0 -3+3a2+a3+a4=0 -1+a2=0
2 1-b2-b4=0 -3-b1-b2-b3+b4=0 3b2+b3+b4=0 b2=0
3 -c2-c4=0 2-c1-c2-c3+c4=0 -2+3c2+c3+c4=0 -1+c2=0
hd V D C p
Thus, 1 f 2 , 3 f ,
k k
Choose four repeating variables , say L,,,Cp and list down the -parameters
M 1 1 LT 2 L3 T 3
a 3 a a a4
h
1
La1 a2 a3 k a4 T 3 L M M ML
1 LT L T
b 3 b
3 3 b b4
g
L 1 2
2 b1 b2 b3 b4 : 2 L M M ML
L k T
1 LT L T
c c 3 c c4
L2 3 3
Cp 1 2
3 2 L M M ML
Lc1 c2 c3 k c4 T
L3 T 3
d d d d4
1 1 LT 1 2 3
4 d d d d M ML
L k
1
L M
2 3 4
1 1 LT 2 L3 T 3
e e4
t
e e
3
5 e1 e2 e3 e4
L k L M M ML
hL
a1=-1: a2=0:a3=0: a4=1 : 1=
k
g L3
b1=-3:b2=2:b3=-2:b4=0: 2= 2
ν
μC p
C1=0: C2=-1: C3=0 :C4=-1: 3=
k
βL2μ 3
d1=-2:d2=-3: d3=2: d4=1: 4= 2
ρ k
T L2 ρ 2 k
e1= -2 : e2=3 ;e3= -2: e4=-1 : 5 =
μ3
Product of 45 will yield another new -parameter [] which can replace 4 and 5 in the
system of governing criteria.
Hence, the system of criteria governing the free convective heat transfer is as follows:
hL gL3 C P
f 2 , , T
k k
gL3 gL3
In practice the criteria , β T are represented by a single dimensionless number βT
ν 2
ν
2
in obtaining the final form of the dimensionless equation in free convective studies. Hence
hL gTL3 C p
f ,
k 2 k
V 2 L2 VL
VL
The importance of the Reynold’s number is if the Reynold’s number is low, then viscous
forces are predominant and the flow is laminar. If Reynold’s number is more than inertial forces
are predominant and the flow is turbulent.
b) Froude number: It is given by a square root of ratio of the inertia forces to gravity forces.
Fi V 2 L2 V
Fe
Fg L g
3
Lg
The importance of Froude number is for dynamic similarity of flow problems where gravity
forces dominate as in the case of spillways, notches, wiers, energy dissipates and wave motion
studies, Froude number must be equal for model and prototype.
c) Euler’s number(Eu): It is given by the square root of the ratio of inertia forces to pressure
forces.
Ei V 2 L2 V
Eu
Ep pL 2
p / p
The importance of Euler number is for dynamic similarity of flow problems where pressure
forces dominant as in the case of pumps and turbines, Euler’s number must be equal for model
and prototype.
d) Weber number (We): It is given by the square root of the ratio of the inertia forces to
surface tension forces.
Fi V 2 L2 V L
We V.
Fs L
L
The importance of the Weber number is for similarity of flow problems where surface
tension forces dominate as in the case of droplet formation, capillary movement of soil moisture
and erosion problems. Weber number must be equal for model and prototype.
e) Mach number (M): It is given by square root of ratio of the inertia forces to elastic forces.
V 2 L2 V
M
KL 2
K/
V
M
C
The importance of Mach number is for similarity of flow problems where elastic forces
are dominant as in the case of rockets, missiles, spacecraft carriers etc., Mach number must be
equal for model and prototype.
f) Grashoff Number: It is the ratio of buoyant force to the viscous force acting on the fluid
denoted by Gr.
Buoyancy force g. .V g.TV g .TL3
Gr .
viscous force 2 2 2
This number provides main criteria in determining whether the flow is laminar or
Turbulent in natural convection
g) Prandtl Number: The relative thickness of velocity and thermal boundaries is best described
by the dimensionless parameter Prandtl number. It id defined as the molecular diffusivity of
C p
momentum to that of molecular diffusivity of heat. Pr . Low prandtl number
K
indicates the heat diffusion at a faster rate and high Prandl number significances slow
dissipation in oils relative to momentum diffusion. Consequently thermal boundary layer in
thickness for liquid metals and thinner for oils relative to velocity boundary layer.
h) Nusselt number: It is the ratio of heat flux by convection to that of heat flux by conduction
when the fluid is assumed motionless.
qconvection hT h
Nu It is represent the enhancement of heat transfer through a
qconduction KT / K
fluid layer as a result of convection relative to conduction across the same fluid layer. Nusselt
number 1 represents the heat transfer is by pure conduction.
i) Peclet number(Pe): is the ratio of heat flow rate by convection to flow rate by conduction
under a unit temperature gradient and through thickness l.
Qconvection mC p AV C p
kAt kA
Qcoduction
l l
Qconvection AV C p C p lV
Pe lV
Qconduction kA / l k
The peclet number can be recast as
C p lV C p
Pe lV Re Pr
k k
i.e. the Peclet number is a function of Reynolds number and Pandtl number.
j) Stanton number: St is the ratio of heat transfer coefficient to the flow of heat per unit
temperature rise due to the velocity of the fluid.
h
St
VC p
hl / k Nu
Vl / C p / k Re Pr
Thus the Stanton number can be expressed terms of other dimensionless number as:
Nusselt number
St
Reynolds number Pandtl number
It should be noted that Stanton number can be used only in correlating forced convection
data. Through dimensional analysis, we have obtained the following possible forms for
correlation of convection data. (Ref Problem 7.9 and 7.10)
In Forced convection: Nu f1 Re, Pr or St f 2 Re, Pr and
In Free convection: Nu f 2 Gr, Pr
Thus, the classification of the regions is done zone wise viz., viscous and invisid regions.
Viscous region confines to the range - 0<y< (known as boundary layer)
Invisid or non-viscous region is beyond y>
The thermal boundary layer t can be different from the , the hydrodynamic boundary layer
depending on the thermal properties of the medium viz.,, the kinematic viscosity and the thermal
diffusivity.
The relation between velocity and thermal boundary layers is given below.
t
Pr 1 / 3
It can be seen from this relationship the physical significance of the dimensionless number, Pr,
i.e
For gases: Pr=1,=1(thickness of thermal boundary layer= thickness of hydrodynamic boundary
layer)
For viscous liquids: Pr >1;1 (thickness of thermal boundary layer < thickness of
hydrodynamic boundary layer)
For molten metals: Pr<1: >1 (thickness of thermal boundary layer > thickness of
hydrodynamic boundary layer)
Thus average heat transfer coefficient over the entire surface can be found using the above
equation.
The above expression is valid for the assumption that the velocity profile is a third degree
polynomial. However the profile may not follow the rule exactly. And it is found that exact value
of the local drag coefficient is
0.664
f
Re x
The average friction factor is obtained using
L
1
L
f avg f x dx
0
2. f x
1.328
f avg
Re L1 / 2
4.96 x
x
Re x
The drag force acting on the plate
1
F f . . A.u 2
2
Assuming the temperature profile as
2 3
y y y
a 0 a1 a 2 a3 and following the energy integral approach we get
t t t
t
0.976 Pr 1 / 3
Nu x 0.332 Pr1 / 3 Re x
1/ 2
Which is valid for Re < 5105 and Pr for 0.6 < Pr<10 and for very high values of Prantdl
number.
Pohlhausen’s exact calculations shown that the local Nusselt number is given by
Nu x 0.339 Pr1 / 3 Re x
1/ 2
The velocity profile in turbulent flow is experimentally determined and represented with a power
1/ 7
u y
law distribution as and the shear force acting one the plate is empirically expressed
u
as
0.2
u
w . 0.0296 .u 2
y y 0 ux
The boundary layer thickness for completely turbulent starting from leading edge is given by
x 0.381 x Re x 0.2
f
using the colburn analogy St Pr 2 / 3 as in (5.53)
2
we obtain St x Pr 2 / 3 0.0296 Re x 0.2
Nu x
Pr 2 / 3 0.0296 Re 0.2
Re . Pr
The properties are to be evaluated at film temperature. The average heat transfer coefficient in
turbulent flowcan be obtained as follows
0.8
hx x vx
0.0296 Pr 1 / 3 i.e h x 0.2 Cx .0.2
K
L L
1 1
havg hx dx Cx 0.2 dx
L L
0 0
havg 1.25 hL
Nuavg 0.036 Pr 0.33 Re L 0.8 17400 297 Pr1 / 3
4.6.2. Empirical correlations for forced convective heat transfer over horizontal
pipes/cylinders
Flow over a cylinder is more of practical importance as in the case of radiators, heat
exchangers and condenser tubes etc. The determination of friction coefficient and heat transfer
is very complicated due to the complexicity of flow around cylinder. Consider a fluid flowing
across a cylinder with a velocity U as shown in the figure. The flow Reynolds number can be
.u D
found using Re D .
At higher Reynolds number the vertices start in the wake region and the velocity and
temperature distribution around the cylinders becomes most complicated. The drag force acting
1 u 2
on the cylinder is expressed as F C D . . A.
2 2
Where CD is known as drag coefficient. At low Reynolds number the drag is caused by viscous
force only and the boundary layer is attached to the cylinder. In that condition the drag is
maximum. As Reynolds number increases the drag is partly due to wake formation and partly
due to viscous force. If Reynolds number exceeds 5000 the drag is predominantly by the high
turbulent eddies formed in the wake region. When the flow separation occurs i.e. nearly at Re =
4.5105 the drag coefficient suddenly drops, which reduces the size of wake and hence the drag.
Whitaker presents the average Nusselt number for flow over the cylinder as
Pr
0.25
0.5 0.06 2/3 0.4
Nu 0.4 Re Re
w
T T
where the physical properties are evaluated at free stream temperature T f w except w
2
which is evaluated at wall temperature.
For gases the viscosity effects are neglected and the properties are evaluated at film temperature.
The general equation to predict average Nusselt number for gases and liquids is given by
Nu C Re n Pr1 / 3
ReD C n
0.4 to 4 0.989 0.33
4 to 40 0.911 0.385
40 to 4000 0.683 0.466
4000 to 40000 0.193 0.618
40000 to 400000 0.027 0.805
Whenever fluid flows through a pipe, the difference in temperature between the fluid and
pipe causes the heat transfer to occur by convection. The nature of flow can be determined by
finding the Reynolds number.
d
.v.d .v.d 4 m 4m
Re .
d d . d
4 4
where m Av is the mass flow rate through the pipe. If the Reynolds number is >2300
the flow is turbulent else it is laminar. Since the value of is very less in the order of 10-6
generally Reynolds number is more than 2300 in most of the practical cases and the flow is
turbulent. The heat transfer and friction factor correlations are mostly empirical in nature.
Experimental determination of friction factor by knowing the pressure drop and hence the heat
transfer coefficient is the easiest method.
So it is of more interest and useful to know the average Nusselt number considering the entrance
length effects also. Hausen has developed an empirical formula to determine the average Nusselt
number considering the effects in entry region for constant wall temperature as
D
0.668 Re . Pr
Nu 3.66 L
avg 2/3
D
1 0.04 Re . Pr
L
D
where Re D . Pr Gz a dimensionless number known as Gratez number (Gz).
L
All properties are to be evaluated at bulk mean temperature.
4.10.1 Laminar flow: Let us consider a hot plate with coordinate system as shown in
Fig.10.2.Assume an isothermal condition i.e. the wall temperature is maintained constant and the
flow is laminar.
The governing equation for this are
u v
0
x y
u u 2u
u v g T T
x y y 2
T T 2T
u v
x y y 2
4
or Nuavg Nulocal
3
Thus the general expression for Nusselt number in a simplified form as Nu c.Gr. Pr n c.Ra n
The value of c and n are for laminar flow is c = 0.59 and n = ¼, under uniform wall temperature
T T
conditions. The Gr and Pr are evaluated at film temperature, T f w .
2
Nu 0.59 Ra 0.25
and for uniform wall heat flux condition Sparrow and Gregg have developed expression based on
experimental data for water as
UNIT-V
Regenerative Heat Exchanger: A Porous medium generally of metal balls, pebbles, powder etc
called bed or Matrix through which hot and cold fluids are passed alternatively. Thus during the
flow of hot fluid the bed absorbs heat and when cold fluid is passed the heat is transferred from
the bed to the cold fluid. In some regenerators half of the bed is exposed to hot fluid and other
half to the cold fluid. During rotation the bed periodically passes through hot stream and then
through the cold stream. However this kind of rotary regenerators are useful for gas-to- gas heat
exchange and not useful for liquid since the heat capacity of bed is less for liquids.
However most of the heat exchanger can be brought under common classification i.e
parallel flow, counter flow and cross flow heat exchangers.
Compact heat exchangers: when the surface area to volume ratio of a heat exchanger is greater
than 750 m2/ m3 the heat exchanger is known as compact heat exchanger. Generally when one of
the fluids is gas and having small heat transfer coefficient it requires large surface area and a
compact heat exchanger is best suitable. The fig 44 shows different kinds of compact heat
exchangers. In the case of compact heat exchangers the pressure drop of the fluid will be high
and is of important design consideration. In many cases the heat transfer characteristics and
friction factor of such configurations is found experimentally. Several Researches have done
extensive work on compact heat exchangers and developed charts to obtain heat transfer and
friction factors, for a specified matrix and Reynolds number. Thus the value of U for a compact
heat exchanger can be obtained from these charts and applying either LMTD or NTU method we
can estimate the rate of heat transfer and its size requirements etc.
fluid and heat gain by cold fluid.
Q mh ch Thi Tho
mc cc Tco Tci
5.4. Overall heat transfer coefficient
The heat has to flow through three resistances namely convective resistance of inside
fluid, conduction resistance of the tube surface and convective resistance of cold fluid. All these
resistances act in series.Let at any instant of time or position the temperature of hot fluid is Th
and cold fluid is Tc. Then the heat transfer can be expressed as
T
Q
Rtotal
1 1 r 1
RTotal ln 2
ho Ao 2KL r1 hi Ai
Where L represent the total length of the pipe. The combined conduction and convective
resistance of the pipe can be expressed as overall heat transfer coefficient as follows.
1
RTotal
U o Ao
Where Uo is known as overall heat transfer coefficient based on outside surface area.
ΔT
Q U o Ao Δ T
Rtotal
Where Δ T is the effective temperature difference between hot fluid and cold fluid.
1 1 r2 1
RTotal R f ln Rf -
i hi Ai 2KL r1 ho Ao o
This fouling factor considerably increases the resistance of the exchanger and thus affects the
heat transfer rate. The value of fouling factor depends on the type of fluids flowing through the
pipes.
The magnitude of scaling factor depends on the nature of the deposits and is generally
built up of unknown complicated composites.
Generally fouling factors will be given in m2K/W. where as the other convective and
conduction resistances are in kW. Hence in the above equation while using R f and R f , care
i o
must be taken to substitute in proper units.
1 1
Resistance due to scale r -
U clean U fouled
Q mc cc Tco Tci
Let d Th Tc dTh dTc
dQ dQ 1 1
dQ
mh ch mc cc mh ch mc cc
1 1
d Th Tc UdATh Tc
mh ch mc cc
d Th Tc
UdA
Th i Th o
Tc o Tc i
Th Tc Q Q
Integrating on both sides between the limits inlet to outlet.
Tout
d Th Tc UA
Th Tc
Q
Th o Tc o Th i Tc i
Tin
Th o Tc o UA
ln
Th i Tc i
Q
Th o Tc o Th i Tc i
Th Tc o Thi Tc i
Q UA o
Th o Tc o
ln
Th i Tc i
T out T in
UA
T out
ln
T in
= UA [LMTD]
Where LMTD is the logarithmic temperature
difference, which is nothing but the effective
temperature difference to be considered.
Total heat transfer is given by
Q mh C h Thi Tho
Q mcCc Tco Tci
Consider d Th Tc dTh dTc
dQ dQ 1 1
dQ
mh ch mc cc mh ch mc cc
Thi Tho Tco Tci
d Th Tc UdATh Tc
Q Q
d Th Tc UdA
Th Tc
Q
Tho Tci Thi Tco
Integrating both sides between inlet and outlet conditions
Tout
d Th Tc UA
Tho Tci Thi Tco
Th Tc Q
Tin
T T
ln ho ci
Thi Tco
UA
Q
Tho Tco Thi Tci
Q UA
Th o Tci Thi Tc o
Th o Tc i
ln
Th i Tc o
T out T in
Q UA
T out
ln
T in
= UA[LMTD]
Case i:
Let us assume the cold fluid enters at Tci and if max heat transfer occurs between the
fluids it can come out at Tco=Thi;
Maximum heat transfer = mc cc Tc o Tc i mc cc Th i Tc i
The heat capacity of hot fluid mh ch Cc
The heat capacity of hot fluid mc cc Ch
It is obvious from fig that Th i Th o is less than
Tc o Tc i or Th i Tc i
i.e. the cold fluid is subjected to maximum
temperature difference.
Q mh c h Δ T hot fluid mc cc Δ T cold fluid
C h Δ T hot C c Δ T cold
since ΔT cold is more that Δ T hot to satisfy the above
equation
C h Cc or Cc must be minimum
The maximum possible heat transfer can be express as
Case (ii):
Let us assume the cold fluid is getting heated up from Tc i to Tc o and the hot fluid is
entering at Th i in the counter flow direction. If maximum possible heat transfer occurs Th i will be
cooled up to Tci and hence Th o Tc i
Maximum heat transfer Qmax mh ch Th i Th o
mh ch Th i Tc i
it is obvious from the figure that Th i Tc i or
Th i Th o is greater that Tc o Tc i i.e. the
hot fluid is subjected to maximum
temperature difference.
Q mh c h Δ T hot mc cc Δ T cold
Q C h Δ T hot C c Δ T cold
since the ΔT hot is greater than Δ T cold to satisfy the above equation Ch must be minimum.
Hence
Qmax mh ch Th i Tc i Cmin Th i Tc i
Th i Tc i
C h Th i Th o C T Tc i
From the definition of ε c co
Cmin Th i Tc i C min Th i Tc i
from which we can get
Th o Th i
Cmin
Th i Tc i .
Ch
1 1
1 1 UA
1 ε .Cmin . e C h Cc
Cc Ch
1 1 UA Cc
UA 1
1 e Cc C h
1 e
Cc C h
ε
1 1 C min C c
C min . 1
C c C h Cc C h
If we assume Cc is minimum then
UA C min
1
1 e N 1 C
C min C max
1 e
C min 1 C
1
C max
where C = Cmin/Cmax known as heat capacity ratio
1 e N 1 C
-
1 C
If C = 1 i.e. if heat capacity of both fluids is same as in the case of regenerator of a gas turbine.
ε 1 e 2 N 12
That is if N the max = 50%.
If C = 0, ε 1 e N which is in the case of condensers and evaporators.
Th o Tc i
d Th Tc 1 1
A
Th i Tc o
Th Tc
U dA
Cc C h o
C h Th i Th o C T Tc i
From the definition of ε c co
C min Th i Tc i C min Th i Tc i
Th o Th i
Cmin
Th i Tc i .
Ch
Tc o Tc i
Cmin
Th i Tc i .
Cc
Substituting these in the equation 14.17b and integrating, we get
Th i Tc i min Th i Tc i .
C
1 1
Cc e UA Cc Ch
Th i
C min
Th i Tc i Tc i
Ch
Th i Tc i Cmin Thi Tci . UA 1 1
Cc
e c h
C C
Th i Tc i C min
Th i Tc i .
Ch
C min
1 . 1
UA
1
Cc
e c h
C C
C
1 min .
Ch
1 1 1 1
UA UA
C
1 min . e Cc C h e C c C h C min
.
C
Cc c
C 1
UA
1
C min
1
UA
1
min
.e Cc C h
e Cc C h
1.
Cc Cc
1 1
UA
1 e Cc C h
1 1
1
UA
1
C min .e h
C c C
Cc C h
Let Cc = Cmin
UA Cc
1
1 e
Cc C h
C min C UA 1 Cc
1 c .e Cc Ch
Cc Ch
UA Cmin
1
1 e Cmax
Cmin
C min C UA Cmin
1
1 min .e min Ch
C
C max Ch
1 e N 1C
1 C.e N 1C
e N 1C .N
C.e N 1C .N e N 1C
N 1
If N = 1.
N 1 1 1
N
When C = 0, 1 e N
So the maximum possible effectiveness incase of counter flow heat exchanger is 100% where as
for a parallel flow the maximum effectiveness is only 50%.
C
Incase of boilers, evaporators and condensers min 0 . Substituting this in respective
Cmax
expressions for effectiveness in parallel flow and counter flow.
effectiveness (parallel flow) = 1 e N
effectiveness (counter flow) = 1 e N
HEAT TRANSFER COURSE MATERIAL (A36C2)
UNIT-VI
6. Boiling:
Phase – I: When the surface temperature of the coil is around 50 greater than the saturation
temperature the liquid near the surface of the coil gets slightly superheated. Then convection
currents setup and circulate the liquid causing evaporation at the surface. This regime is called
interface evaporation.
Phase – II: With further rise in temperature the bubbles began to form on the surface of the wire
at certain spots and they eventually condense in the liquid without rising to the surface.
Phase – III: With further increase in temperature difference, the bubbles start forming on the
surface more rapidly and rise to the surface of liquid resulting in rapid evaporation. This occurs
at a temperature difference of 500C. In this phase the amount of heat flux reaches maximum and
is known as critical heat flux represented by point A as shown in the pool-boiling curve of fig.
11.9. The order of heat flux is expected around 1 MW/m2.
The second and third phases in which the bubbles develop and grow is known as
Nucleate boiling. The maximum heat flux occurred is known as critical heat flux. And from here
the boiling crisis will begin.
Phase – IV: As the heating continues the bubbles on the surface of the heating rod form so
rapidly that they tend to blanket the heating surface with an vapor film. This vapor film thus
formed on the heating surface prevents the inflow of fresh liquid from taking their place. The
heat now has to be transferred into the liquid through this film, to effect any further boiling and
hence known as film boiling. Since the thermal conductivity of this film is much less than liquid
the value of heat flux starts decreasing with increase in temperature difference.
In the critical stages the bubbles formed on the surface forms a film but collapse immediately
and form rapidly. Thus the film formed is an unstable film.
Phase – V: With further growth in the temperature the film stabilizes and the heating surface is
completely covered with a blanket of vapor and the heat flux reaches its lowest value.
Phase – VI: The surface temperature required for maintaining a stable film is very high and
under these conditions a considerable amount of heat starts entering into the liquid by radiation
and the heat flux starts increasing. To reach the maximum heat flux experienced in nucleate
boiling in the film boiling the surface temperature must be raised to a very high value more than
15000C at which the heating surface may itself burn. This point is called burnout point.
The rate of heat transfer is found high in the nucleate boiling and least in the stable film
boiling.
Eg: A droplet of water when sprinkled on a red hot pan doesn’t evaporate immediately,
but dances few times on the pan surface. This is due to the formation of stable film at the
interface between the hot surface and liquid droplet. Once this film is broken the droplet
suddenly evaporates and escapes to the atmosphere.
6.3. Condensation
Condensation of a vapor occurs when it is cooled sufficiently below the saturation
temperature, to induce the nucleation of droplets. Such nucleation may be homogeneous within
the matter like formation of fog in winter or heterogeneously on the entrained particulate matter
like in expansion of steam in steam turbine or in condensation on the tube surface of a steam
condenser etc.. This kind of condensation is divided into two types a) Film condensation b) Drop
wise condensation.
Film condensation occurs on the cold surface which can be easily wetted. On non –
wetted surfaces the vapor condense in drops which grow by further condensation and
coalescence and then roll over the surface. New drops take their place.
6.3.1. Film condensation Vs Drop wise condensation.
Film condensation occurs on the surfaces which are clean and uncontaminated. The vapor
condenses on the surface spreads out and forms a continuous film over the entire surface. The
liquid thus formed flows down the surface due to gravity and the film thickness grows due to
continuous condensation of vapors. This film covering the surface offers resistance for heat
exchange between vapor and cold surface and reduces the rate of condensation.
Drop wise condensation occurs on the rough surfaces or surfaces having dents, cracks
etc.. This may also occur on surfaces contaminated with impurities like fatty acids and organic
compounds. In this type of condensation the vapor condenses on the surface in the form of
droplets. These droplets stick to the surface due to the roughness or the dents on the surface. The
droplet size gradually increases and it breaks away from the surface falling down due to gravity
and in the process knocks of other droplets. Thus a continuous film is not developed and the cold
surface is again exposed to the vapors afresh. Therefore the rate of condensation is very high and
it experiences a high heat flux at the surface. The condensing heat transfer coefficient in drop
wise condensation is found 7 to 10 times more than film wise condensation. Thus to promote
drop wise condensation the surface is artificially coated with chemical substances that inhibits
wetting. Teflon, wax, oils and fatty acids are often used for this. It is found that coating the
surface with noble metals like gold will also enhance drop wise condensation. However
sustaining the drop wise condensation for a long time is highly difficult due to its unstable
nature. The droplets formed on the surface gradually fills the rough pores or dents thereby
making the surface smooth and the process eventually turns into a film wise condensation. Due
to this reason only, in the design of industrial condensers the heat transfer coefficient considered
is only based on film wise condensation. The table lists the major difference between the two.
Table: Film condensation versus Drop wise condensation
Film condensation Drop wise condensation
The condensate tends to wet the surface Condensate doesn’t wet the surface.
and forms a liquid film Only part of the surface is covered with
Heat transfer is through film. Since the condensate and heat transfer is directly
entire surface is covered with a liquid between surface and vapor.
film. High heat transfer rates are reported due
The rate of heat transfer is low due to to good contact between vapor and
the resistance offered by liquid film. surface.
1 g y2
0
y dy
2
g. 2
Um
3
Considering the energy balance, i.e. the rate of heat transfer through conduction in film is equal
to heat transfer by convection
dQ K .
dx.W
TS Tw h.dx.W TS Tw
K
hx
The mass flow rate of steam through a section at a distance x is given by mx W U m .
g 2 2 g 3
Mass flow rate = .
3 3
The amount of condensate leaving the element at x x is
m x dx m x
d
m x x
dx
Increase in mass flow rate = m
d
m x .x
dx
d 2 g 3
.x
dx 3
2g d 3
.
3 dx
.x
2 g d 3 d
. .dx
3 d dx
2 g 2
m .d
Under steady state condition
K
3 d
1
Ts Tw .dx Integrating
.
g h fg
2
4 K
Ts Tw x c2
4 gh fg
2
c2 0
1/ 4
4 kxT
2 g.h fg
we get
1/ 4
k 3 2 g .h fg
k
hx
4xT
The average heat transfer coefficient over the length L is
L
1 4
havg hx dx havg hx
L 3
0
1/ 4
4 k g .h fg
3 2
havg
3 4 LTs Tw
1/ 4
k 3 2 g.h fg
havg 0.943
LTs Tw
To account for the various assumptions made in the above theory based on experimental
results the value of h during laminar film condensation is proposed by Machine Adams as
1/ 4
k 3 2 g .h fg
havg 1.13
LTs Tw
The properties in the above equation are to be evaluated at mean film temperature i.e. at
T Ts
Tf w
2
Q havg .L.wTs Tw
The total mass of condensate formed m
h fg h fg
If the surface is inclined, the value of g is replaced by g sin where is the angle made by the
surface with horizontal.
0.25
k 3 2 g sin
hinclined 0.943
LTw Tw
h
inclined sin 0.25 This is applicable for 60 90 0
hvertical
vDh 4A
The critical Reynolds number Re where Dh is the hydraulic mean diameter .The
p
critical Reynolds number is considered as 1800 and when Re>1800 the flow is turbulent.
The average heat transfer coefficient for turbulent condition is proposed by Kirkbide as
3 2 1 / 3
0.4 k g
hturbulent 0.077 Re
2