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,
which is equal to the latitude of the location. The system is
made vapour tight to prevent leakage of thermal energy.
Experiments were conducted from 9 a.m. to 17 p.m.
from22 September 2011 to 23 October 2011 and the energy,
exergy and entropies have been calculated for one of the
typical days, i.e. 27 September 2011. The average solar
radiation for the typical day is above 700 W/m
2
. Glass and
wick temperatures were recorded with the calibrated cop-
per constantan thermocouples (range between 100
C and
300
C.
Energy balance equations for the inner surface of the
glass cover, outer surface of the glass cover, moist air and
wick surface have been written in terms of solar radiation
and ambient temperature. The equations have been solved
to obtain the analytical solutions and used to evaluate the
thermal performance of the still.
3. Energy analysis
The thermal modelling of the single-slope oating-cum-
tilted wick-type solar still has been proposed based on the
energy balance equations for the temperature elements of
the system and written as
Inner surface of the glass cover (T
gi
):
g
I (t)
g
g
l
g
b
g
+h1(T
w
T
gi
)l
w
b
w
+h
2
(T
m
T
gi
)l
m
b
m
= h3(T
gi
T
go
)l
gi
b
gi
. (1)
Equation (1) is solved to obtain
T
gi
=
g
I (t)
g
g
l
g
b
g
+h1(T
w
T
gi
)l
w
b
w
+h
2
(T
m
T
gi
)l
m
b
m
+h
3
(T
gi
T
go
)l
gi
b
gi
h1l
w
b
w
+h2l
m
b
m
+h3l
gi
b
gi
. (2)
Outer surface of the glass cover (T
go
):
g
I (t)
g
l
g
b
g
+h3(T
gi
T
go
)l
gi
b
gi
= h4(T
go
T
a
)l
go
b
go
.
(3)
Equation (3) is solved to obtain
T
go
=
g
I (t)
g
l
g
b
g
+h3T
gi
l
gi
b
gi
+h4T
a
l
go
b
go
h3l
gi
b
gi
+h4l
go
b
go
. (4)
For moist air (T
m
)
I (t)
g
g
+h(T
w
T
m
)l
w
b
w
= h2(T
m
T
gi
)l
m
b
m
+h5(T
m
T
a
)l
m
b
m
. (5)
Equation (5) is solved to obtain
T
m
=
I (t)
g
g
+h(T
w
)l
w
b
w
+h2(T
gi
)l
m
b
m
+h5(T
a
)l
m
b
m
hl
w
b
w
+h2l
m
b
m
+h5l
m
b
m
.
(6)
For the evaporating wick surface
g
I (t)
g
g
l
g
b
g
= M
w
dT
w
dt
l
w
b
w
+h1(T
w
T
gi
)l
w
b
w
+h(T
w
T
m
)l
w
b
w
+h6(T
w
T
a
)l
w
b
w
.
(7)
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International Journal of Ambient Energy 3
Figure 1. (a). Schematic diagram of the wick-type passive solar still and (b) photograph of the experimental still.
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4 V. Manikandan et al.
Substituting the value for T
gi
in Equation (7), the
equation becomes
g
I (t)
g
g
l
g
b
g
= M
w
dT
w
dt
l
w
b
w
+h1
_
_
_
_
T
w
_
_
_
_
g
I (t)
g
g
l
g
b
g
+h1(T
w
T
gi
)l
w
b
w
+h2(T
m
T
gi
)l
m
b
m
+h3(T
gi
T
go
)l
gi
b
gi
h1l
w
b
w
+h2l
m
b
m
+h3l
gi
b
gi
_
_
_
_
_
_
l
w
b
w
+h(T
w
T
m
)l
w
b
w
+h6(T
w
T
a
)l
w
b
w
. (8)
After a suitable rearrangement, the equation takes the form
as
g
I (t)
g
g
l
g
b
g
+
h1
g
I (t)
g
g
l
g
b
g
M
w
(h1l
w
b
w
+h2l
m
b
m
+h3l
gi
b
gi
)
+T
m
_
h1h2l
m
b
m
M
w
(h1l
w
b
w
+h2l
m
b
m
+h3l
gi
b
gi
)
h
M
w
_
+T
go
_
h3l
gi
b
gi
M
w
(h1l
w
b
w
+h2l
m
b
m
+h3l
gi
b
gi
)
_
+
h6T
w
M
w
h6T
a
M
w
=
dT
w
dt
+T
w
_
h
1
+h
M
w
h1l
w
b
w
M
w
(h1l
w
b
w
+h2l
m
b
m
+h3l
gi
b
gi
)
_
.
(9)
Equation (9) resembles the form
dy
dx
+Py = Q, (10)
P =
_
h1 +h
M
w
h1l
w
b
w
M
w
(h1l
w
b
w
+h2l
m
b
m
+h3l
gi
b
gi
)
_
,
Q =
g
I (t)
g
g
l
g
b
g
+
h1
g
I (t)
g
g
l
g
b
g
M
w
(h1l
w
b
w
+h2l
m
b
m
+h3l
gi
b
gi
)
+T
m
_
h1h2l
m
b
m
M
w
(h1l
w
b
w
+h2l
m
b
m
+h3l
gi
b
gi
)
h
M
w
_
+T
go
_
h3l
gi
b
gi
M
w
(h1l
w
b
w
+h2l
m
b
m
+h3l
gi
b
gi
)
_
+
h6T
w
M
w
h6T
a
M
w
.
The solutions of the Equation (10) is given by
T
w
e
_
P,dt
=
_
Q(t), e
_
P,dt
dt +c. (11)
when t = 0, T
w
= T
wi
, we obtain
c = T
wi
Q
P
Substituting the value for c in Equation (11), the solution
for T
w
can be written as
T
w
=
Q
P
_
T
wo
Q
P
_
e
Pt
. (12)
The mass of the distillate yield obtained is given by
M
ewgi
=
h
ewgi
(T
w
T
gi
)
L
30 60
_
kg
m
2
30 min
_
. (13)
The instantaneous eciency of the wick-type passive solar
still is given by
i
=
M
ewgi
L
_
I (t) dt
100. (14)
3.1. Exergy analysis
The most appropriate tool for optimisation and thermody-
namic analysis process is exergyanalysis. The methodology
is a combinationof rst andsecondlaws of thermodynamics
accompanied with the environmental conditions. An exergy
analysis is similar to an energy analysis, but takes into
account the quality of the energy as well as the quantity.
The exergy balance of any system can be represented as
(Total exergy entering) (Total exergy leaving)
(Total exergy destroyed)
= (change in total exergy of the system)
Ex
in
Ex
out
Ex
destroyed
= Ex.
In other words, exergy can be simply expressed as the ratio
of exergy output associated with the product of the single-
basin single-slope wick-type solar still (i.e. distillate) to the
exergy input given to the same still (i.e. radiation from the
sun)
Ex =
Exergy output from the wick type single basin
single slope solar still
Exergy input to the wick type single basin
single slope solar still
Ex =
Ex
out
Ex
in
,
Ex =
Ex
evaporation
Ex
sun
. (15)
Therefore, the maximum eciency ratio for evaluating
exergy of solar radiation obtained to the proposed still at
temperature T
sun
can be expressed as
Ex
in
I (t), in(t)
Ex
sun
I (t), sun(t)
=
_
1
4
3
_
T
a
T
s
_
+
1
3
_
T
a
T
s
_
4
_
, (16)
where T
s
is the surface temperature of the sun = 6000 K.
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International Journal of Ambient Energy 5
Figure 2. Schematic exergy ow diagram of the still.
The evaporative heat ux is required to evaporate water
from the wick surface of area A
w
, and can be written as
Q
ewgi
= h
ewgi
A
w
(T
w
T
gi
). (17)
Therefore, the exergy output of the system can be obtained
as
Ex
out
= Ex
evaporation
= h
ewgi
A
w
(T
w
T
gi
)
_
1
T
a
T
w
_
.
(18)
With the exergy input and output for the components of the
still, the instantaneous exergy eciency of the system can
be expressed as
Ex
instan
=
Q
ewgi
_
1
T
a
T
w
_
EX
sun
=
h
ewgi
A
w
(T
w
T
g
)
l
g
b
g
l(t)
g
_
1
T
a
T
w
_
_
1
4
3
_
T
a
T
s
+
1
3
_
T
a
T
s
_
4
__. (19)
Ex
instan
=
i
_
_
_
_
T
w
T
a
T
w
_
1
4
3
_
T
a
T
s
+
1
3
_
T
a
T
s
_
4
__
_
_
,
Ex
instan
=
i
1
z
(T
w
T
a
)
T
w
. (20)
where,
z =
_
1
4
3
_
T
a
T
s
+
1
3
_
T
a
T
s
_
4
__
.
The exergy ow diagram is represented in Figure 2. The
numbers from 0 to 7 indicate the exergy ow of the system
in a numerical order.
In the still, the brackish water enters the distillation sys-
tem at 303 K and 3000 ppm salinity. These values are taken
as the conditions of dead state of the system.
The mass fractions of the salt and water in the water
tank lled with brackish water are W
s
= 0.003 and w
w
=
1 W
s
= 0.997. Therefore, the exergy of a owstream()
can be determined from the following equation:
= h h
0
T
0
(s s
0
). (21)
Therefore, the specic enthalpy and specic entropy of the
ow stream can be found out by the following formulae.
For ideal solution, the enthalpy and entropy of the mixture
are the sum of the enthalpy and entropy of its individual
components and they are given by
H = m
s
h
s
+m
w
h
w
and S = m
s
s
s
+m
w
s
w
,
where
h = w
s
h
s
+w
w
h
w
and S = w
s
s
s
+w
w
s
w
.
Therefore,
h
s
= h
s0
+c
ps
(T T
0
),
s
s
= s
s0
+c
ps
ln
_
T
T
0
_
Rln
_
P
P
0
_
.
(22)
As there is no pressure for incompressible substance, so the
above equation can be written as
s
s
= s
s0
+c
ps
ln
_
T
T
0
_
. (23)
Therefore, by determining the values of specic enthalpy
and specic entropy of a ow stream, the exergy of a ow
stream () can be obtained from the following equation:
= h h
0
T
0
(s s
0
). (24)
Table 1 gives the thermodynamic values for the owstream
at initial temperature during the early working hour of the
system.
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Table 1. Thermodynamic values of dierent streams at initial temperature.
Specic Specic Specic heat
S. Temperature Enthalpy h Entropy S enthalpy entropy Gas capacity
No. Stream (K) (kJ/kg K) (kJ/kg K) (kJ/kg K) (kJ/kg K) constant R (kJ/kg K)
1 0 (brine water) 303 167.71 6.701 213.4053 0.4013 0.287 1.006
2 1 (tank water) 303 167.71 6.701 213.4053 0.4013 0.287 1.006
3 2 (wick surface) 325 145.554 6.769 217.1452 0.7276 0.287 1.008
4 3 (moist air) 327 143.538 6.775 225.5059 0.7532 0.287 1.008
5 4 (inner glass cover) 323 147.569 6.762 208.7855 0.7018 0.287 1.008
6 5 (condensate) 323 147.568 6.762 208.7855 0.7018 0.287 1.008
7 6 (brine out) 305 165.697 6.708 133.5655 0.4621 0.287 1.007
8 7 (output) 303 167.71 6.701 213.4053 0.4013 0.287 1.006
9 8 (outer glass cover) 321 149.584 6.759 200.4262 0.6758 0.287 1.008
The complete exergy ow of the system depends on the
amount of exergyavailable inthe systemtothe exergygoing
out and the exergy destroyed inside the system. The exergy
destroyed in the system can be evaluated by the equation.
3.2. Exergy destroyed brine
Exergy destroyed in the brine water is
Ex
destroyed,brine
= Ex
in,brine
w
min,brine
, (25)
where
Ex
in,brine
= A
g
I (t)
_
1
4
3
_
T
a
T
s
_
+
1
3
_
T
a
T
s
_
4
_
and
w
min,brine
=
RT
0
M
w
__
M
w
rM
m
1
__
x
s
, brine ln
x
s
, brine
x
s
+ x
w
brine ln
x
w
, brine
x
w
_
ln x
w
_
,
%Ex
destroyed,brine
=
Ex
destroyed,brine
Ex
in
. (26)
3.3. Exergy destroyed in moist air
The exergy destroyed in moist air is
Ex
destroyed,moist air
= Ex
in,moist air
w
min,moist air
, (27)
where
Ex
in,moist air
= A
g
I (t)
_
1
4
3
_
T
a
T
s
_
+
1
3
_
T
a
T
s
_
4
_
and
w
min,moist air
=
RT
0
M
w
__
M
w
rM
m
1
_
_
x
s
, moist air ln
x
s
, moist air
x
s
+ x
w
moist ln
x
w
, moist air
x
w
_
ln x
w
_
%Ex
destroyed,moist air
=
Ex
destroyed,moist air
Ex
in
(28)
4. Entropy analysis
The entropy of a system is associated with the presence
of irreversibility. The entropy generation takes place in a
system due to the irreversible nature of heat transfer and
viscosity eects, within the uid and at the solid bound-
aries. The largest boundary uxes or entropy is associated
with the emission of long-wave radiation. On the planetary
scale, the mean outgoing ux of entropy at the top of the
atmosphere is found to be about 22 times larger than the
mean incoming ux of entropy through solar radiation. The
entropy production terms involve the release of latent heat
and the absorption of solar radiation and the destruction
is mainly accomplished through cooling by the outgoing
long-wave radiation.
The entropy and specic entropy of the proposed still
have been coined under the exergy conditions of the still.
Therefore, the increase and decrease in entropy during the
working hours of the still and the conversion of vapours in
the still can be found by the following equations.
The change in entropy during the variation of tempera-
ture is given by
s1 =
_
T
2
T
1
dQ
T
= mc
_
T
2
T
1
dT
T
(29)
where m = mass of the water in (kg), c = specic heat
of water (KJ/kg K), T
2
= nal temperature of water in a
particular interval of time (K), T
1
= initial temperature of
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International Journal of Ambient Energy 7
water (273 +initial temperature, K) and L = latent heat of
water (J/kg).
Therefore, the increase in entropy of a system can be
given by
s1 = 2.3026 mc (log
10
T
2
log
10
T
1
). (30)
The change in entropy when saline is converted into
vapour at a particular temperature is given by
s2 =
dQ
T
=
mL
T
, (31)
where m = mass of the saline water (kg) and L = latent
heat of water (J/kg)
Hence, the total entropy of the system can be found by
nding the total increase in entropy of the system
s = s1 +s2. (32)
5. Results and discussion
5.1. Energy analysis
The energy analysis based on Dunckles law of thermody-
namics completely ignores the quality of the energy and
only tracks the quantity and does not give the quantitative
assessment of the various losses occurring in the parameters
of a system. Therefore, a better method for energy account-
ing is exergy analysis, which is based on both the rst and
second law of thermodynamics.
Figure 3 shows the variation of solar irradiance and
ambient temperature with respect to time of the proposed
still during the daylight hours from 9:00 a.m. to 17:00 p.m.
From the graph, it is observed that the tilted solar radi-
ation available on the glass cover gradually increases and
reaches a maximumof 1215 W/m
2
at 12 p.m. and gradually
decreases till 17 p.m. The maximum ambient tempera-
ture of 40
C)
h
ewm
evaporative heat transfer coecient from wick
surface to moist air (W/m
2
C)
h
rgigo
radiative heat transfer coecient from inner to
outer surface of the glass cover (W/m
2
C)
h
rgoa
radiative heat transfer coecient fromouter surface
of the glass cover to ambient (W/m
2
C)
h
rmgi
radiative heat transfer coecient from moist air to
inner surface of the glass cover (W/m
2
C)
h
rwgi
radiative heat transfer coecient from wick surface
to inner surface of the glass cover (W/m
2
C)
h
rwm
rradiative heat transfer coecient from wick
surface to moist air (W/m
2
C)
h
s
enthalpy of salt in wick (kJ)
h
s0
enthalpy of salt (kJ/kg K)
h
w
enthalpy of water in wick (kJ)
r recovery ratio (%)
s specic entropy of the stream (kJ/kg)
s
0
specic entropy of the stream at the dead state
(kJ/kg)
A
g
area of the glass cover (m
2
)
A
w
area of the wick surface (m
2
)
I (t)
g
tilted solar radiation over the glass cover (W/m
2
)
L
i
thickness of the insulation (m)
M
dwt
mass of the distillate output (kg/m
2
)
M
ewgi
mass of evaporative heat transfer coecient from
wick surface to the inner surface of the glass
cover (W/m
2
C)
M
m
molar mass of the mixture (kg/kmol)
M
w
mass of the water in the wick surface
(kg/m
2
/30 min)
Q
ewgi
rate of evaporative heat transfer coecient from
wick surface to the inner surface of the glass
cover (W/m
2
C)
T
0
dead state temperature of the still (
C)
T
a
ambient temperature (
C)
T
gi
temperature of the inner surface of the glass cover
(
C)
T
g0
temperature of the outer surface of the glass cover
(
C)
T
m
moist air temperature (
C)
T
s
surface temperature of the sun (
C)
T
w
temperature of the wick surface (
C)
R gas constant (kJ/Kmol)
L latent heat of vaporisation (J/kg)
T temperature of the stream (
C)
Symbols
g
absorptivity of the glass cover
g
temperature of the glass (
C)
i
instantaneous energy eciency of the system
exergy ow of the stream (kJ/kg)
References
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