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CHAPTER 8
CHANGE OF STATE
Most substances can exist in three states, i.e. solid, liquid and gas. Water, for example,
may exist in the form of ice, water or steam. A transition from one of these states to
another is called a phase change. The change from one phase to another takes place very
abruptly at a defined temperature. The temperature at which a phase change occurs
depends on quantities such as pressure.
As more heat is added the temperature does not rise, but the ice gradually melts into
water. The temperature remains constant until all the ice has melted (Fig. 8.2). Then, as
more heat is added, the temperature of water steadily increases until point D is reached.
Again, the temperature remains constant until all the water has been converted into
vapour. Then, additional heat will increase the temperature of that vapour.
Fig.8.2
If this experiment is repeated at a lower pressure, the phase changes occur at B' and D'
(Fig. 8.1). But the temperatures corresponding to the phase changes at B' and D' are
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Steam also behaves the same as gas. When 1 kg of steam at 100 °C turns to water, it gives
off 2.255 x 106 J of heat. The heat absorbed in converting water into steam is released in
exact amount when converting steam back into water. The heat supplied in converting
water into steam at 100 °C is stored by the steam. When the steam turns to water, all of
such stored heat (same as the amount of heat taken) is released. This is an example of
conservation of heat (energy).
Since the latent heat of fusion of ice is 3.3 35 105 J kg-1, we get
Q =Lm
Q =3.335 105 J kg-1 5 kg
=1.67 106 J
Example (2) Ice cubes at - 10 °C with a total mass of 0.045 kg are mixed with 0.3 kg tea
at 30 °C. What is the final equilibrium temperature? (The specific heat capacity of tea is
the same as that of water.)
Assume that all the ice melts. If this is correct, the final temperature calculated must be
higher man 0 °C.
The heat needed to bring the ice to 0 °C is
Ql =micecice
= 0.045 2089 10
= 940.05 J
The heat needed to melt the ice is
Q2 =Lmice
=3.335 105 0.045
= 15 007 . 5 J
The heat needed to warm the melted ice from 0 °C to the final temperature T is
Q3 = micc C
= 0.045 4169 (T-0)
= 187.61 T J
The heat lost by the tea, originally at 30 °C, is
Q4 =mteactea
=0.3 4169 (30-T)
= (37 521-1 250.7 T) J
Since the heat lost must equal the heat gained,
Q4 =Q1 + Q2 + Q3
37 521- 1 250.7 T = 940.05 + 15 007.5+187.61 T
1 438.31 T =21 573.45
T =15°C
The final temperature is higher than 0 °C. Therefore, the original assumption that all the
ice melts is correct.
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Example (3) Replace the tea in the preceding example by 0.045 kg of water at 30 °C.
What is the equilibrium condition?
Assume provisionally that the ice melts completely.
To melt 1 kg of ice 3.335 105 J of heat are required. Suppose that 3.335 105 J of heat
are enough to cool m kg of water from 30 °C to 0 °C.
Since equal masses of ice and water are given, it is clear that not all the ice melts.
Therefore, the original assumption is wrong. The final temperature of the mixture of ice
and water must be 0 oC.
As in example (2). the heat required to raise the temperature of ice to 0 °C is
Q1 = 940.05 J
The heat required to melt a mass m1 of ice is
Q2 =Lm .
=3.335 l05 m1 J
The heat lost by the water, originally at 30°C, is
Q3 =mwatercvvater
= 0.045 4169 30 = 5628.15 J
Equating the heat gained to the heat lost, we get
940.05 + 3.335 l05 m1 =5628.15
m1 = 0.014kg
Only 0.014 kg out of 0.045 kg of ice melts. In the final equilibrium condition 0.045 -
0.014 = 0.031 kg of ice mixes with 0.045 + 0.014 = 0.059 kg of water.
Fig. 8.3
It was mentioned that the boiling point of water varies with the atmospheric pressure. An
increase in external pressure will raise the boiling point of water. This is used in pressure
cookers (Fig. 8.4). When a pressure cooker is in operation, the pressure inside it is twice
the normal atmospheric pressure. At this pressure water boils at a higher temperature of
120 °C and thus food can be cooked in a much shorter time.
Fig. 8.4 A pressure cooker reduces cooking time by raising the boiling point of
the water inside it.
Fig. 8.5 An aerosol can: applying the effect of increased pressure on boiling.
Another application of the effect of increased pressure on boiling is in aerosol can such as
those for hair sprays and insecticide sprays ( Fig. 8.5). In one form of aerosol spray, the
propellant liquid is mixed with the insecticide. The pressure in the container is kept high,
so that the propellant does not vaporize. When the button is pressed, a valve opens and
the pressure is released. At the reduced pressure, the propellant quickly vaporizes or
boils. In the process, the propellant expands, pushing the insecticide out in the form of a
spray. It is dangerous to throw aerosol cans into a fire since if heated to high
temperatures, the propellant boils despite the high pressure. The propellant expands even
though the release button is pressed and this may cause an explosion.
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At higher altitudes, the pressure is lower. Water boils at a temperature lower than 100 °C.
The boiling point of water is thus an indication of the altitude. Boiling at low
temperatures under reduced pressure is very useful. It requires less energy to boil off the
unwanted water. This method is cheaper because less fuel is used. In a sugar mill, sugar
solution is made by mixing the cane sugar with water. The solution is boiled at 60 °C
under reduced pressure until granulated sugar crystals separate out. This is cheaper than
boiling it at 100 °C. Furthermore low temperature boiling does not brown the sugar.
The detailed account of variation of the boiling point of water is illustrated by the
vaporization curve in Fig. 8.4. The variation of the values of boiling point with pressure
is more obvious than that of the values of melting point of ice with pressure. This means
that the effect of pressure on the boiling point of water is greater than that on the melting
point of ice.
Fig.8.4
In order to see clearly the variation of the boiling point of water with change in pressure
from 1000 mm Hg to 2000 mm Hg, the enlarged graph for that pressure range is shown
separately in the dotted frame.
The point at the top of the vaporization curve is called critical point. At temperatures
above that point, the substance cannot exist in liquid phase. However much the pressure
is increased, the liquid phase can never exist at all. The critical temperature of helium is
the lowest. It is - 268.9 °C or 4.26 K. Helium exists as a gas at temperatures above this
value.
SUMMARY
Most substances can exist in three states, i.e. solid, liquid and gas. A transition from
one these states to another is called a phase change.
The change from one phase to another takes place very abruptly at a definite
temperature.
The temperature at which a phase change occurs depends on quantities such a
pressure.
A direct change from the solid phase to the gas phase is called sublimation.
At the triple point, liquid, solid and vapour phases may all exist together.
At the critical point a kilogram of liquid and a kilogram of gas have the same
volume, and the distinction between the two phases vanishes.
The energy absorbed or liberated in a phase change is called the latent heat.
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which comprise
Solid so
lid
ifi
ca
me tio
lt in n
g
Melting point
lowered by increased pressure Liquid co
Freezing point nd
en
lowered by presence of impurities bo sa
ev tio
Latent heat of fussion Lf and ap ilin g n
specific latent heat of fussion lf or o
at r
io
Lf = mlf where n
Lf = latent heat of fussion (J) Gas
m = mass (kg)
lf = specific latent heat of
fussion (Jkg-1)
Boiling point
increased by presence of impurities
lowered by reduced pressure
raised by increased pressure
Latent heat of vaporisation Lv and
specific latent heat of vaporisation lv
Lv = mlv where
Lv = latent heat of vaporisation (J)
m = mass (kg)
lv = specific latent heat of
vaporisation (Jkg-1)
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EXERCISES