CHAPTER-11

THRMAL PROPERTIES OF MATTER

PAGE-294
EXERCISE

Question 11.1:

The triple points of neon and carbon dioxide are 24.57 K and 216.55 K respectively. Express
these temperatures on the Celsius and Fahrenheit scales.

• Answer
•
• Discussion

Kelvin and Celsius scales are related as:

TC = TK – 273.15 … (i)

Celsius and Fahrenheit scales are related as:

… (ii)

For neon:

TK = 24.57 K

∴ TC = 24.57 – 273.15 = –248.58°C

For carbon dioxide:

TK = 216.55 K

∴ TC= 216.55 – 273.15 = –56.60°C

Question 11.2:

Two absolute scales A and B have triple points of water defined to be 200 A and 350 B. What
is the relation between TA and TB?

• Answer
•
• Discussion

Triple point of water on absolute scaleA, T1 = 200 A

Triple point of water on absolute scale B, T2 = 350 B

Triple point of water on Kelvin scale, TK = 273.15 K

The temperature 273.15 K on Kelvin scale is equivalent to 200 A on absolute scale A.

T1 = TK

200 A = 273.15 K

The temperature 273.15 K on Kelvin scale is equivalent to 350 B on absolute scale B.

T2 = TK

350 B = 273.15

TA is triple point of water on scale A.

TB is triple point of water on scale B.

Therefore, the ratio TA : TB is given as 4 : 7.

Question 11.3:

The electrical resistance in ohms of a certain thermometer varies with temperature according
to the approximate law:

R = Ro [1 + α (T – To)]

The resistance is 101.6 Ω at the triple-point of water 273.16 K, and 165.5 Ω at the normal
melting point of lead (600.5 K). What is the temperature when the resistance is 123.4 Ω?

• Answer
•
• Discussion

It is given that:

R = R0 [1 + α (T – T0)] … (i)

Where,

R0 and T0 are the initial resistance and temperature respectively

R and T are the final resistance and temperature respectively

α is a constant

At the triple point of water, T0 = 273.15 K

Resistance of lead, R0 = 101.6 Ω

At normal melting point of lead, T = 600.5 K

Resistance of lead, R = 165.5 Ω

Substituting these values in equation (i), we get:

For resistance, R1 = 123.4 Ω

Question 11.4:

Answer the following:

(a) The triple-point of water is a standard fixed point in modern thermometry. Why? What is
wrong in taking the melting point of ice and the boiling point of water as standard fixed points
(as was originally done in the Celsius scale)?

(b) There were two fixed points in the original Celsius scale as mentioned above which were
assigned the number 0 °C and 100 °C respectively. On the absolute scale, one of the fixed
points is the triple-point of water, which on the Kelvin absolute scale is assigned the number
273.16 K. What is the other fixed point on this (Kelvin) scale?

(c) The absolute temperature (Kelvin scale) T is related to the temperature tc on the Celsius
scale by
tc = T – 273.15

Why do we have 273.15 in this relation, and not 273.16?

(d) What is the temperature of the triple-point of water on an absolute scale whose unit
interval size is equal to that of the Fahrenheit scale?

• Answer
•
• Discussion

(a) The triple point of water has a unique value of 273.16 K. At particular values of volume
and pressure, the triple point of water is always 273.16 K. The melting point of ice and boiling
point of water do not have particular values because these points depend on pressure and
temperature.

(b) The absolute zero or 0 K is the other fixed point on the Kelvin absolute scale.

(c) The temperature 273.16 K is the triple point of water. It is not the melting point of ice.
The temperature 0°C on Celsius scale is the melting point of ice. Its corresponding value on
Kelvin scale is 273.15 K.

Hence, absolute temperature (Kelvin scale) T, is related to temperature tc, on Celsius scale as:

tc = T – 273.15

(d) Let TF be the temperature on Fahrenheit scale and TK be the temperature on absolute
scale. Both the temperatures can be related as:

Let TF1 be the temperature on Fahrenheit scale and TK1 be the temperature on absolute scale.
Both the temperatures can be related as:

It is given that:

TK1 – TK = 1 K

Subtracting equation (i) from equation (ii), we get:

Triple point of water = 273.16 K

∴ Triple point of water on absolute scale = = 491.69

PAGE-295

Question 11.5:

Two ideal gas thermometers Aand Buse oxygen and hydrogen respectively. The following
observations are made:

Temperature Pressure thermometer A Pressure thermometer B

Triple-point of water 1.250 × 105 Pa 0.200 × 105 Pa

Normal melting point of sulphur 1.797 × 105 Pa 0.287 × 105 Pa

(a) What is the absolute temperature of normal melting point of sulphur as read by
thermometers Aand B?

(b) What do you think is the reason behind the slight difference in answers of thermometers
Aand B? (The thermometers are not faulty). What further procedure is needed in the
experiment to reduce the discrepancy between the two readings?

• Answer
•
• Discussion

(a) Triple point of water, T = 273.16 K.

At this temperature, pressure in thermometer A, PA = 1.250 × 105 Pa

Let T1 be the normal melting point of sulphur.

At this temperature, pressure in thermometer A, P1 = 1.797 × 105 Pa

According to Charles’ law, we have the relation:

= 392.69 K

Therefore, the absolute temperature of the normal melting point of sulphur as read by
thermometer A is 392.69 K.

At triple point 273.16 K, the pressure in thermometer B, PB = 0.200 × 105 Pa

At temperature T1, the pressure in thermometer B, P2 = 0.287 × 105 Pa

According to Charles’ law, we can write the relation:

Therefore, the absolute temperature of the normal melting point of sulphur as read by
thermometer B is 391.98 K.

(b) The oxygen and hydrogen gas present in thermometers A and B respectively are not
perfect ideal gases. Hence, there is a slight difference between the readings of thermometers
A and B.

To reduce the discrepancy between the two readings, the experiment should be carried under
low pressure conditions. At low pressure, these gases behave as perfect ideal gases.

Question 11.6:
A steel tape 1m long is correctly calibrated for a temperature of 27.0 °C. The length of a steel
rod measured by this tape is found to be 63.0 cm on a hot day when the temperature is 45.0
°C. What is the actual length of the steel rod on that day? What is the length of the same steel
rod on a day when the temperature is 27.0 °C? Coefficient of linear expansion of steel = 1.20
× 10–5 K–1.

• Answer
•
• Discussion

Length of the steel tape at temperature T = 27°C, l = 1 m = 100 cm

At temperature T1 = 45°C, the length of the steel rod, l1 = 63 cm

Coefficient of linear expansion of steel, α = 1.20 × 10–5 K–1

Let l2 be the actual length of the steel rod and l' be the length of the steel tape at 45°C.

Hence, the actual length of the steel rod measured by the steel tape at 45°C can be calculated
as:

= 63.0136 cm

Therefore, the actual length of the rod at 45.0°C is 63.0136 cm. Its length at 27.0°C is 63.0
cm.

Question 11.7:

A large steel wheel is to be fitted on to a shaft of the same material. At 27 °C, the outer
diameter of the shaft is 8.70 cm and the diameter of the central hole in the wheel is 8.69 cm.
The shaft is cooled using ‘dry ice’. At what temperature of the shaft does the wheel slip on the
shaft? Assume coefficient of linear expansion of the steel to be constant over the required
temperature range: α steel = 1.20 × 10–5 K–1.

• Answer
•
 • Discussion

The given temperature, T = 27°C can be written in Kelvin as:

27 + 273 = 300 K

Outer diameter of the steel shaft at T, d1 = 8.70 cm

Diameter of the central hole in the wheel at T, d2 = 8.69 cm

Coefficient of linear expansion of steel, α steel = 1.20 × 10–5 K–1

After the shaft is cooled using ‘dry ice’, its temperature becomes T1.

The wheel will slip on the shaft, if the change in diameter, Δd = 8.69 – 8.70

= – 0.01 cm

Temperature T1, can be calculated from the relation:

Δd = d1α steel (T1 – T)

0.01 = 8.70 × 1.20 × 10–5 (T1 – 300)

(T1 – 300) = 95.78

∴ T1= 204.21 K

= 204.21 – 273.16

= –68.95°C

Therefore, the wheel will slip on the shaft when the temperature of the shaft is –69°C.

Question 11.8:

A hole is drilled in a copper sheet. The diameter of the hole is 4.24 cm at 27.0 °C. What is the
change in the diameter of the hole when the sheet is heated to 227 °C? Coefficient of linear
expansion of copper = 1.70 × 10–5 K–1.

• Answer
•
• Discussion

Initial temperature, T1 = 27.0°C

Diameter of the hole at T1, d1 = 4.24 cm

Final temperature, T2 = 227°C

Diameter of the hole at T2 = d2

Co-efficient of linear expansion of copper, α Cu = 1.70 × 10–5 K–1

For co-efficient of superficial expansion β,and change in temperature ΔT, we have the relation:

Change in diameter = d2 – d1 = 4.2544 – 4.24 = 0.0144 cm

Hence, the diameter increases by 1.44 × 10–2 cm.

Question 11.9:

A brass wire 1.8 m long at 27 °C is held taut with little tension between two rigid supports. If
the wire is cooled to a temperature of –39 °C, what is the tension developed in the wire, if its
diameter is 2.0 mm? Co-efficient of linear expansion of brass = 2.0 × 10–5 K–1; Young’s
modulus of brass = 0.91 × 1011 Pa.

• Answer
 •
• Discussion

Initial temperature, T1 = 27°C

Length of the brass wire at T1, l = 1.8 m

Final temperature, T2 = –39°C

Diameter of the wire, d = 2.0 mm = 2 × 10–3 m

Tension developed in the wire = F

Coefficient of linear expansion of brass, α = 2.0 × 10–5 K–1

Young’s modulus of brass, Y = 0.91 × 1011 Pa

Young’s modulus is given by the relation:

Where,

F = Tension developed in the wire

A = Area of cross-section of the wire.

ΔL = Change in the length, given by the relation:

ΔL = α L(T2 – T1) … (ii)

Equating equations (i) and (ii), we get:

(The negative sign indicates that the tension is directed inward.)

Hence, the tension developed in the wire is 3.8 ×102 N.

Question 11.10:

A brass rod of length 50 cm and diameter 3.0 mm is joined to a steel rod of the same length
and diameter. What is the change in length of the combined rod at 250 °C, if the original
lengths are at 40.0 °C? Is there a ‘thermal stress’ developed at the junction? The ends of the
rod are free to expand (Co-efficient of linear expansion of brass = 2.0 × 10–5 K–1, steel = 1.2 ×
10–5 K–1).

• Answer
•
• Discussion

Initial temperature, T1 = 40°C

Final temperature, T2 = 250°C

Change in temperature, ΔT = T2 – T1 = 210°C

Length of the brass rod at T1, l1 = 50 cm

Diameter of the brass rod at T1, d1 = 3.0 mm

Length of the steel rod at T2, l2 = 50 cm

Diameter of the steel rod at T2, d2 = 3.0 mm

Coefficient of linear expansion of brass, α 1 = 2.0 × 10–5K–1

Coefficient of linear expansion of steel, α 2 = 1.2 × 10–5K–1

For the expansion in the brass rod, we have:

For the expansion in the steel rod, we have:

Total change in the lengths of brass and steel,

Δl = Δl1 + Δl2

= 0.2205 + 0.126

= 0.346 cm

Total change in the length of the combined rod = 0.346 cm

Since the rod expands freely from both ends, no thermal stress is developed at the junction.

Question 11.11:

The coefficient of volume expansion of glycerin is 49 × 10–5 K–1. What is the fractional change
in its density for a 30 °C rise in temperature?

• Answer
•
• Discussion

Coefficient of volume expansion of glycerin, α V = 49 × 10–5 K–1

Rise in temperature, ΔT = 30°C

Fractional change in its volume =

This change is related with the change in temperature as:

Where,

m = Mass of glycerine

= Initial density at T1

= Final density at T2

Where,

= Fractional change in density

∴ Fractional change in the density of glycerin = 49 ×10–5 × 30 = 1.47 × 10–2

Question 11.12:

A 10 kW drilling machine is used to drill a bore in a small aluminium block of mass 8.0 kg.
How much is the rise in temperature of the block in 2.5 minutes, assuming 50% of power is
used up in heating the machine itself or lost to the surroundings. Specific heat of aluminium =
0.91 J g–1 K–1.

• Answer
 •
• Discussion

Power of the drilling machine, P = 10 kW = 10 × 103 W

Mass of the aluminum block, m = 8.0 kg = 8 × 103 g

Time for which the machine is used, t = 2.5 min = 2.5 × 60 = 150 s

Specific heat of aluminium, c = 0.91 J g–1 K–1

Rise in the temperature of the block after drilling = δT

Total energy of the drilling machine = Pt

= 10 × 103 × 150

= 1.5 × 106 J

It is given that only 50% of the power is useful.

Therefore, in 2.5 minutes of drilling, the rise in the temperature of the block is 103°C

Question 11.13:

A copper block of mass 2.5 kg is heated in a furnace to a temperature of 500 °C and then
placed on a large ice block. What is the maximum amount of ice that can melt? (Specific heat
of copper = 0.39 J g–1 K–1; heat of fusion of water = 335 J g–1).

• Answer
•
• Discussion

Mass of the copper block, m = 2.5 kg = 2500 g

Rise in the temperature of the copper block, Δθ = 500°C

Specific heat of copper, C = 0.39 J g–1 °C–1

Heat of fusion of water, L = 335 J g–1

The maximum heat the copper block can lose, Q = mCΔθ

= 2500 × 0.39 × 500

= 487500 J

Let m1 g be the amount of ice that melts when the copper block is placed on the ice block.

The heat gained by the melted ice, Q = m1L

Hence, the maximum amount of ice that can melt is 1.45 kg.

Question 11.14:

In an experiment on the specific heat of a metal, a 0.20 kg block of the metal at 150 °C is
dropped in a copper calorimeter (of water equivalent 0.025 kg) containing 150 cm3 of water at
27 °C. The final temperature is 40 °C. Compute the specific heat of the metal. If heat losses to
the surroundings are not negligible, is your answer greater or smaller than the actual value for
specific heat of the metal?

• Answer
•
• Discussion

Mass of the metal, m = 0.20 kg = 200 g

Initial temperature of the metal, T1 = 150°C

Final temperature of the metal, T2 = 40°C

Calorimeter has water equivalent of mass, m’ = 0.025 kg = 25 g

Volume of water, V = 150 cm3

Mass (M) of water at temperature T = 27°C:

150 × 1 = 150 g

Fall in the temperature of the metal:

ΔT = T1 – T2 = 150 – 40 = 110°C
Specific heat of water, Cw = 4.186 J/g/°K

Specific heat of the metal = C

Heat lost by the metal, θ = mCΔT … (i)

Rise in the temperature of the water and calorimeter system:

ΔT′’ = 40 – 27 = 13°C

Heat gained by the water and calorimeter system:

Δθ′′ = m1 CwΔT’

= (M + m′) Cw ΔT’ … (ii)

Heat lost by the metal = Heat gained by the water and colorimeter system

mCΔT = (M + m’) Cw ΔT’

200 × C × 110 = (150 + 25) × 4.186 × 13

If some heat is lost to the surroundings, then the value of C will be smaller than the actual
value.

PAGE-296

Question 11.15:

Given below are observations on molar specific heats at room temperature of some common
gases.

Molar specific heat (Cv)

Gas
(cal mol–1 K–1)

Hydrogen 4.87

Nitrogen 4.97
 Oxygen 5.02

Nitric oxide 4.99

Carbon monoxide 5.01

Chlorine 6.17

The measured molar specific heats of these gases are markedly different from those for
monatomic gases. Typically, molar specific heat of a monatomic gas is 2.92 cal/mol K. Explain
this difference. What can you infer from the somewhat larger (than the rest) value for
chlorine?

• Answer
•
• Discussion

The gases listed in the given table are diatomic. Besides the translational degree of freedom,
they have other degrees of freedom (modes of motion).

Heat must be supplied to increase the temperature of these gases. This increases the average
energy of all the modes of motion. Hence, the molar specific heat of diatomic gases is more
than that of monatomic gases.

If only rotational mode of motion is considered, then the molar specific heat of a diatomic

With the exception of chlorine, all the observations in the given table agree with . This
is because at room temperature, chlorine also has vibrational modes of motion besides
rotational and translational modes of motion.

Question 11.16:

Answer the following questions based on the P-T phase diagram of carbon dioxide:

(a) At what temperature and pressure can the solid, liquid and vapour phases of CO2 co-exist
in equilibrium?
(b) What is the effect of decrease of pressure on the fusion and boiling point of CO2?

(c) What are the critical temperature and pressure for CO2? What is their significance?

(d) Is CO2 solid, liquid or gas at (a) –70 °C under 1 atm, (b) –60 °C under 10 atm, (c) 15 °C
under 56 atm?

• Answer
•
• Discussion

(a) The P-T phase diagram for CO2 is shown in the following figure.

C is the triple point of the CO2 phase diagram. This means that at the temperature and
pressure corresponding to this point (i.e., at –56.6°C and 5.11 atm), the solid, liquid, and
vaporous phases of CO2 co-exist in equilibrium.

(b) The fusion and boiling points of CO2 decrease with a decrease in pressure.

(c) The critical temperature and critical pressure of CO2 are 31.1°C and 73 atm respectively.
Even if it is compressed to a pressure greater than 73 atm, CO2 will not liquefy above the
critical temperature.

(d) It can be concluded from the P-T phase diagram of CO2 that:

(a) CO2 is gaseous at –70°C, under 1 atm pressure

(b) CO2 is solid at –60°C, under 10 atm pressure

(c) CO2 is liquid at 15°C, under 56 atm pressure

Question 11.16:
Answer the following questions based on the P-T phase diagram of carbon dioxide:

(a) At what temperature and pressure can the solid, liquid and vapour phases of CO2 co-exist
in equilibrium?

(b) What is the effect of decrease of pressure on the fusion and boiling point of CO2?

(c) What are the critical temperature and pressure for CO2? What is their significance?

(d) Is CO2 solid, liquid or gas at (a) –70 °C under 1 atm, (b) –60 °C under 10 atm, (c) 15 °C
under 56 atm?

• Answer
•
• Discussion

(a) The P-T phase diagram for CO2 is shown in the following figure.

C is the triple point of the CO2 phase diagram. This means that at the temperature and
pressure corresponding to this point (i.e., at –56.6°C and 5.11 atm), the solid, liquid, and
vaporous phases of CO2 co-exist in equilibrium.

(b) The fusion and boiling points of CO2 decrease with a decrease in pressure.

(c) The critical temperature and critical pressure of CO2 are 31.1°C and 73 atm respectively.
Even if it is compressed to a pressure greater than 73 atm, CO2 will not liquefy above the
critical temperature.

(d) It can be concluded from the P-T phase diagram of CO2 that:

(a) CO2 is gaseous at –70°C, under 1 atm pressure

(b) CO2 is solid at –60°C, under 10 atm pressure

(c) CO2 is liquid at 15°C, under 56 atm pressure

Question 11.17:

Answer the following questions based on the P–T phase diagram of CO2:

(a) CO2 at 1 atm pressure and temperature – 60 °C is compressed isothermally. Does it go

through a liquid phase?

(b) What happens when CO2 at 4 atm pressure is cooled from room temperature at constant
pressure?

(c) Describe qualitatively the changes in a given mass of solid CO2 at 10 atm pressure and
temperature –65 °C as it is heated up to room temperature at constant pressure.

(d) CO2 is heated to a temperature 70 °C and compressed isothermally. What changes in its
properties do you expect to observe?

• Answer
•
• Discussion

Answer:

(a) No

(b) It condenses to solid directly.

(c) The fusion and boiling points are given by the intersection point where this parallel line
cuts the fusion and vaporisation curves.

(d) It departs from ideal gas behaviour as pressure increases.

Explanation:

(a) The P-T phase diagram for CO2 is shown in the following figure.
At 1 atm pressure and at –60°C, CO2 lies to the left of –56.6°C (triple point C). Hence, it lies
in the region of vaporous and solid phases.

Thus, CO2 condenses into the solid state directly, without going through the liquid state.

(b) At 4 atm pressure, CO2 lies below 5.11 atm (triple point C). Hence, it lies in the region of
vaporous and solid phases. Thus, it condenses into the solid state directly, without passing
through the liquid state.

(c) When the temperature of a mass of solid CO2 (at 10 atm pressure and at –65°C) is
increased, it changes to the liquid phase and then to the vaporous phase. It forms a line
parallel to the temperature axis at 10 atm. The fusion and boiling points are given by the
intersection point where this parallel line cuts the fusion and vaporisation curves.

(d) If CO2 is heated to 70°C and compressed isothermally, then it will not exhibit any
transition to the liquid state. This is because 70°C is higher than the critical temperature of
CO2. It will remain in the vapour state, but will depart from its ideal behaviour as pressure
increases.

Question 11.18:

A child running a temperature of 101°F is given an antipyrin (i.e. a medicine that lowers fever)
which causes an increase in the rate of evaporation of sweat from his body. If the fever is
brought down to 98 °F in 20 min, what is the average rate of extra evaporation caused, by the
drug? Assume the evaporation mechanism to be the only way by which heat is lost. The mass
of the child is 30 kg. The specific heat of human body is approximately the same as that of
water, and latent heat of evaporation of water at that temperature is about 580 cal g–1.

• Answer
•
• Discussion

Initial temperature of the body of the child, T1 = 101°F

Final temperature of the body of the child, T2 = 98°F

Change in temperature, ΔT = °C

Time taken to reduce the temperature, t = 20 min

Mass of the child, m = 30 kg = 30 × 103 g

Specific heat of the human body = Specific heat of water = c

= 1000 cal/kg/ °C

Latent heat of evaporation of water, L = 580 cal g–1

The heat lost by the child is given as:

Let m1 be the mass of the water evaporated from the child’s body in 20 min.

Loss of heat through water is given by:

∴ Average rate of extra evaporation caused by the drug

Question 11.19:

A ‘thermacole’ icebox is a cheap and efficient method for storing small quantities of cooked
food in summer in particular. A cubical icebox of side 30 cm has a thickness of 5.0 cm. If 4.0
kg of ice is put in the box, estimate the amount of ice remaining after 6 h. The outside
temperature is 45 °C, and co-efficient of thermal conductivity of thermacole is 0.01 J s–1 m–1
K–1. [Heat of fusion of water = 335 × 103 J kg–1]

• Answer
•
• Discussion

Side of the given cubical ice box, s = 30 cm = 0.3 m

Thickness of the ice box, l = 5.0 cm = 0.05 m

Mass of ice kept in the ice box, m = 4 kg

Time gap, t = 6 h = 6 × 60 × 60 s

Outside temperature, T = 45°C

Coefficient of thermal conductivity of thermacole, K = 0.01 J s–1 m–1 K–1

Heat of fusion of water, L = 335 × 103 J kg–1

Let m’ be the total amount of ice that melts in 6 h.

The amount of heat lost by the food:

Where,

A = Surface area of the box = 6s2 = 6 × (0.3)2 = 0.54 m3

Mass of ice left = 4 – 0.313 = 3.687 kg

Hence, the amount of ice remaining after 6 h is 3.687 kg.

Question 11.20:

A brass boiler has a base area of 0.15 m2 and thickness 1.0 cm. It boils water at the rate of
6.0 kg/min when placed on a gas stove. Estimate the temperature of the part of the flame in
contact with the boiler. Thermal conductivity of brass = 109 J s –1
m–1 K–1; Heat of vaporisation
of water = 2256 × 103 J kg–1.

• Answer
•
• Discussion

Base area of the boiler, A = 0.15 m2

Thickness of the boiler, l = 1.0 cm = 0.01 m

Boiling rate of water, R = 6.0 kg/min

Mass, m = 6 kg

Time, t = 1 min = 60 s

Thermal conductivity of brass, K = 109 J s –1

m–1 K–1

Heat of vaporisation, L = 2256 × 103 J kg–1

The amount of heat flowing into water through the brass base of the boiler is given by:

Where,

T1 = Temperature of the flame in contact with the boiler

T2 = Boiling point of water = 100°C

Heat required for boiling the water:

θ = mL … (ii)

Equating equations (i) and (ii), we get:

Therefore, the temperature of the part of the flame in contact with the boiler is 237.98°C.

Question 11.21:

Explain why:

(a) a body with large reflectivity is a poor emitter

(b) a brass tumbler feels much colder than a wooden tray on a chilly day

(c) an optical pyrometer (for measuring high temperatures) calibrated for an ideal black body
radiation gives too low a value for the temperature of a red hot iron piece in the open, but
gives a correct value for the temperature when the same piece is in the furnace

(d) the earth without its atmosphere would be inhospitably cold

(e) heating systems based on circulation of steam are more efficient in warming a building
than those based on circulation of hot water

• Answer
•
• Discussion

(a) A body with a large reflectivity is a poor absorber of light radiations. A poor absorber will
in turn be a poor emitter of radiations. Hence, a body with a large reflectivity is a poor
emitter.

(b) Brass is a good conductor of heat. When one touches a brass tumbler, heat is conducted
from the body to the brass tumbler easily. Hence, the temperature of the body reduces to a
lower value and one feels cooler.
Wood is a poor conductor of heat. When one touches a wooden tray, very little heat is
conducted from the body to the wooden tray. Hence, there is only a negligible drop in the
temperature of the body and one does not feel cool.

Thus, a brass tumbler feels colder than a wooden tray on a chilly day.

(c) An optical pyrometer calibrated for an ideal black body radiation gives too low a value for
temperature of a red hot iron piece kept in the open.

Black body radiation equation is given by:

Where,

E = Energy radiation

T = Temperature of optical pyrometer

To = Temperature of open space

σ = Constant

Hence, an increase in the temperature of open space reduces the radiation energy.

When the same piece of iron is placed in a furnace, the radiation energy, E = σ T4

(d) Without its atmosphere, earth would be inhospitably cold. In the absence of atmospheric
gases, no extra heat will be trapped. All the heat would be radiated back from earth’s surface.

(e) A heating system based on the circulation of steam is more efficient in warming a building
than that based on the circulation of hot water. This is because steam contains surplus heat in
the form of latent heat (540 cal/g).

Question 11.22:

A body cools from 80 °C to 50 °C in 5 minutes. Calculate the time it takes to cool from 60 °C
to 30 °C. The temperature of the surroundings is 20 °C.

• Answer
•
• Discussion

According to Newton’s law of cooling, we have:

Where,

Temperature of the body = T

Temperature of the surroundings = T0 = 20°C

K is a constant

Temperature of the body falls from 80°C to 50°C in time, t = 5 min = 300 s

Integrating equation (i), we get:

The temperature of the body falls from 60°C to 30°C in time = t’

Hence, we get:

Equating equations (ii) and (iii), we get:

Therefore, the time taken to cool the body from 60°C to 30°C is 10 minutes.