Experiment 106: Specific Heat
Analysis
Energy can manifest in many different ways, such as potential,
kinetic, thermal, electrical, chemical, nuclear, and other various forms.
However, one specific form of energy is thoroughly observed and
examined in this experiment, and that is heat energy.
Heat is simply referred to as the energy transferred from one body or
substance to another in physical contact with each other as the result of a
difference in temperature, but to fully grasp and understand the concept of
heat, we must first observe and analyze how it works and how it is applied
to our surroundings. We must first study the relationship between heat
and other forms of energy, particularly how thermal energy is converted to
and from other forms of energy and how it affects matter. To be precise, the
study of thermodynamics.
To begin, thermodynamics is the branch in physical science that deals
with heat and temperature, and their relation to energy, work, radiation,
and other properties of matter. In broad terms, thermodynamics deals with
the transfer of energy from one place to another and from one form to
another.
In this experiment, the focus will be about specific heat and
calorimetry. Specific heat capacity is the amount of heat energy
required to raise the temperature of a substance per unit of mass. The
specific heat capacity of a material is a physical property. It is also an
example of an extensive property since its value is proportional to the
size of the system being examined. In SI units, specific heat capacity
(symbol: c) is the amount of heat in joules required to raise 1 gram of a
substance 1 Kelvin. It may also be expressed as J/kg·K. Specific heat
capacity may be reported in the units of calories per gram degree Celsius,
too. Related values are molar heat capacity, expressed in J/mol·K, and
volumetric heat capacity, given in J/m3·K. Heat capacity is defined as the
ratio of the amount of energy transferred to a material and the change in
temperature that is produced:
C = Q / ΔT
where C is heat capacity, Q is energy (usually expressed in joules), and
ΔT is the change in temperature (usually in degrees Celsius or in
Kelvin). Alternatively, the equation may be written:
Q = CmΔT
Specific heat and heat capacity are related by mass:
C=m*S
Where C is heat capacity, m is mass of a material, and S is specific heat.
Note that since specific heat is per unit mass, its value does not change,
no matter the size of the sample. So, the specific heat of a gallon of water
is the same as the specific heat of a drop of water. It's important to note
the relationship between added heat, specific heat, mass, and
temperature change does not apply during a phase change. The reason
for this is because heat that is added or removed in a phase change does
not alter the temperature.
Moreover, the specific Heat of a substance is the amount of heat needed
to raise the temperature of a unit mass of a substance by 1°. The table
shows the Specific Heats of substances.
Figure 1. Coffee-Cup Calorimeter
The second focus of the experiment is calorimetry. Calorimetry is a
method of measuring the heat transfer within a chemical reaction or
other physical processes, such as a change between different states of
matter. The term "calorimetry" comes from the Latin calor ("heat") and
Greek metron ("measure"), so it means "measuring heat." Devices used to
perform calorimetry measurements are called calorimeters. Refer to
Figure 1 of the coffee-cup calorimeter above. Since heat is a form of
energy, it follows the rules of conservation of energy. If a system is
contained in thermal isolation (in other words, heat cannot enter or leave
the system), then any heat energy that is lost in one part of the system
has to be gained in another part of the system. If you have a good,
thermally isolating thermos, for example, that contains hot coffee, the
coffee will remain hot while sealed in the thermos. If, however, you put
ice into the hot coffee and re-seal it, when you later open it, you will find
that the coffee lost heat and the ice gained heat ... and melted as a result,
thus watering down your coffee. Now let's assume that instead of hot
coffee in a thermos, you had water inside a calorimeter. The calorimeter
is well insulated, and a thermometer is built into the calorimeter to
precisely measure the temperature of the water inside. If we were to
then put ice into the water, it would melt - just like in the coffee
example. But this time, the calorimeter is continually measuring the
temperature of the water. Heat is leaving the water and going into the
ice, causing it to melt, so if you watched the temperature on the
calorimeter, you'd see the temperature of the water dropping.
Eventually, all of the ice would be melted and the water would reach a
new state of thermal equilibrium, in which the temperature is no longer
changing. From the change in temperature in the water, you can then
calculate the amount of heat energy that it took to cause the melting of
the ice.
Furthermore, calorimetry is the science associated with
determining the changes in energy of a system by measuring the heat
exchanged with the surroundings. In physics class (and for some, in
chemistry class), calorimetry labs are frequently performed in order to
determine the heat of reaction or the heat of fusion or the heat of
dissolution or even the specific heat capacity of a metal. These types of
labs are rather popular because the equipment is relatively inexpensive,
and the measurements are usually straightforward. In such labs, a
calorimeter is used. A calorimeter is a device used to measure the
quantity of heat transferred to or from an object. Most students likely do
not remember using such a fancy piece of equipment known as a
calorimeter. Fear not; the reason for the lack of memory is not a sign of
early Alzheimer's. Rather, it is because the calorimeter used in high
school science labs is more commonly referred to as a Styrofoam cup. It
is a coffee cup calorimeter - usually filled with water. The more
sophisticated cases include a lid on the cup with an inserted
thermometer and maybe even a stirrer.
We learned that water will change its temperature when it gains or
loses energy. And in fact, the quantity of energy gained or lost is given
by the equation.
Q = m water • Cwater • ΔTwater
Where Cwater is 4.18 J/g/°C. So, if the mass of water and the temperature
change of the water in the coffee cup calorimeter can be measured, the
quantity of energy gained or lost by the water can be calculated.
The assumption behind the science of calorimetry is that the energy
gained or lost by the water is equal to the energy lost or gained by the
object under study. So, if an attempt is being made to determine the
specific heat of fusion of ice using a coffee cup calorimeter, then the
assumption is that the energy gained by the ice when melting is equal to
the energy lost by the surrounding water. It is assumed that there is a
heat exchange between the ice and the water in the cup and that no
other objects are involved in the heat exchanged.
Q ice =-Q
surroundings = - Q calorimeter
This statement could be placed in equation form as the role of the
Styrofoam in a coffee cup calorimeter is that it reduces the amount of
heat exchange between the water in the coffee cup and the surrounding
air. The value of a lid on the coffee cup is that it also reduces the amount
of heat exchange between the water and the surrounding air. The more
that these other heat exchanges are reduced, the more true that the
above mathematical equation will be. Any error analysis of a calorimetry
experiment must take into consideration the flow of heat from system to
calorimeter to other parts of the surroundings. And any design of a
calorimeter experiment must give attention to reducing the exchanges of
heat between the calorimeter contents and the surroundings.
In thermodynamics, there are three modes of heat transfer-
conduction, convection, and radiation, a representation of all three
modes of heat transfer is shown in Figure 2.
Figure 2. Modes of Heat Transfer
First is conduction, it is the mode of heat transfer particularly in
solids and also for liquid at rest. In this mode of transfer, the heat
transfers from one atom to its neighboring atom through molecular
vibrations. At the molecular level, first heat energy of a higher energy
level molecule converts to vibrating kinetic energy and this kinetic
energy is transferred to neighboring atoms and so on, such that the
process repeats until the temperature difference between two
neighboring atoms is zero.
The second mode of heat transfer is through convection which
particularly occurs in fluids in motion. That is in both liquids and gases
that are in motion. This mode of heat transfer occurs due to the transfer
of energy through bulk mass. In detail, whenever there is a temperature
difference in a fluid, density difference occurs, and motion of fluid starts
as lower density fluid attempts to reach the top of the fluid. During this
motion, mass and energy transfer occurs; thus, heat transfer takes place
which results to convection being the most efficient way to transfer heat.
Lastly, radiation is a mode of heat transfer that enables heat
transfer through a vacuum, or empty space. It is a method of heat
transfer that does not rely upon any contact between the heat source and
the heated object. Heat can be transmitted though empty space by
thermal radiation. Thermal radiation (often called infrared radiation) is a
type electromagnetic radiation (or light). Radiation is a form of energy
transport consisting of electromagnetic waves traveling at the speed of
light. No mass is exchanged, and no medium is required. When visible
light is absorbed by an object, the object converts the short wavelength
light into long wavelength heat. This causes the object to get warmer.
The main difference of the three modes of heat transfer may be visible
through an in-depth explanation of the three modes of heat transfer.
Conduction is the transfer of heat in a material due to molecular motion,
such that energy transfers through matter from particle to particle. In
this mode of heat transfer, a temperature gradient must exist to act as
the potential for the flow of heat. Heat will always flow from high
temperatures to cooler temperatures. The rate of heat transfer for
conduction is governed by Fourier’s Law of Conduction, which
expresses the rate of heat transfer from each end of a medium.
In Figure 3, the conduction rate equation for the Fourier’s Law of
Conduction is given; wherein, Q is the heat flow rate by conduction, k is
the thermal conductivity of body material, A is the cross-sectional area
normal to direction of heat flow, and dT/dx is the temperature gradient.
Figure 3. Fourier’s Law of Conduction
It is important to remember that the negative sign in Fourier’s
equation indicates that the heat flow is in the direction of negative
gradient temperature and that serves to make heat flow positive. The
thermal conductivity k is one of the transport properties like the
viscosity associated with the transport of momentum, diffusion
coefficient associated with the transport of mass. In addition, it provides
an indication of the rate at which heat energy is transferred through a
medium by conduction process. A few assumptions for the use of
Fourier equation: it is in steady state heat conduction, one directional
heat flow, bounding surfaces are isothermal in character that is constant
and uniform temperatures are maintained at the two faces, isotropic and
homogenous material and thermal conductivity k is constant, constant
temperature gradient and linear temperature profile, and no internal
heat generation. Some features of Fourier equation are as follows: it is
valid for all matter solid, liquid, and gas, the vector expression
indicating that heat flow is normal to an isotherm and it is in the
direction of decreasing temperature, it cannot be derived from first
principle, and it helps to define the transport property k.
When it comes to convection, it is the transfer of heat between a
solid surface and the adjacent fluid that is in motion by the actual
movement of the warmed matter. The faster the fluid motion, the greater
the amount of heat transferred via convective heat transfer. The idea of
forced convection occurs when the fluid is forced into motion by a fan,
pump, moving object, or another form of external energy introduced
into the system that results in the fluid flower over the solid surface. On
the other hand, forced convection, or also known as natural convection,
occurs when the fluid is forced into motion by buoyancy forces that are
induced as a result of changes in density due to changes in the
temperature of the fluid. The rate of heat transfer for convection is
governed by Newton’s Law of Cooling.
Newton’s Law of Cooling
Reynold’s number
Wherein, T(t) is the temperature of an object at a certain time, t is
the time, TS is the temperature of the surroundings, T0 is the starting
temperature of the object, and k is a cooling constant that is specific to
the object. All temperatures are in Kelvin, and the k indicated here has a
unit of s-1. The convective heat transfer coefficient “h” is a function of
the Reynold’s number. The more turbulent the flow, the higher the
convective heat transfer coefficient will be. In Figure 3, the equation for
Reynold’s number is given as the ration of inertia forces all over the
viscous forces; wherein, δ is the characteristic length, ρ is the density of
the fluid, V is the volume of the fluid, and μ is the viscous forces acting
onto the fluid.
Meanwhile, radiation is the transfer of heat in the form of
electromagnetic waves that directly transport energy through space.
Radiation heat transfer is temperature dependent, with the fourth
power, and can occur without a medium, or simply in empty space. A
black body is defined as a body that absorbs all energy incident upon it.
It also emits radiation at the maximum rate for a body of a particular
size at a particular temperature. Black bodies are perfect emitters and
absorbers. Black bodies are also known as cavity radiation that refers to
an object or system which absorbs all radiation incident upon it and re-
radiates energy which is characteristic of this radiating system only, not
dependent upon the type of radiation which is incident upon it. The
radiated energy can be considered to be produced by standing wave or
resonant modes of the cavity which is radiating. The amount of
radiation emitted in a given frequency range should be proportional to
the number of modes in that range. The best of classical physics
suggested that all modes had an equal chance of being produced, and
that the number of modes went up proportional to the square of the
frequency. As mentioned earlier, cavity mode is a mode for an
electromagnetic wave in a cavity that must satisfy the condition of zero
electric field at the wall. If the mode is of shorter wavelength, there are
more ways you can fit it into the cavity to meet that condition. Through
the careful analysis by Rayleigh and Jeans showed that the number of
modes was proportional to the frequency squared. From the assumption
that the electromagnetic modes in a cavity were quantized in energy
with the quantum energy equal to Planck’s constant times the frequency,
Planck derived a radiation formula.
Given the Einstein-Bose distribution function in Equation 1, the
average energy per “mode” or “quantum” times the density of such
states is expressed in terms of Equations 2 and 3. From equations 2 and 3
Planck was able to derive the radiation formulas in Equations 4 and 5;
wherein, h is the Planck’s Constant, c is the speed of light, λ is the
wavelength, T is the period, and k is the Boltzmann’s constant.
(1)
(2)
(3)
(4)
(5)
Now that we understand the theories and concepts of
thermodynamics, heat, calorimetry, and specific heat that were stated
above, we can now move on to the experiment. In this experiment, we were
tasked to demonstrate the change in temperature upon mixing the
substance in a calorimeter and be able to calculate the specific heat of solid
metal.
The objectives of the experiment is to use the principles of
calorimetry, specifically the law of heat exchange, when combining objects
with different temperatures, and to use the law of heat exchange in
determining the specific heat of a solid metal. Proceeding to the
experiment, we first filled a beaker with water ¾ full and heat it using the
electric stove. Then, we immersed the metal into the beaker with boiling
water for heating by holding the string and make sure that the metal will
not touch the beaker. While boiling the metal, we also recorded the weight
of the inner cup of the calorimeter and filled it with tap water and recorded
its weight again. We now then prepared for the set-up by putting the
calorimeter cup into the outer shell with the cover, thermometer, and
stirrer. Then, we recorded the temperature of the water in thermal
equilibrium inside the calorimeter. After 20 minutes of boiling the metal,
we immediately add it into the calorimeter that we’ve prepared and then
we stirred it gently and waited for the reading of the thermometer to
become stable and record it. To calculate for the experimental value of
specific heat of the metal, we used the equation:
QLOSS (metal) + QGAINED (calorimeter & water) = 0
We then compared the experimental value and the accepted value of
specific heats of metal and computed the percentage error.
Table 1. Determining the Specific Heat of a Metal Specimen
Mass of Metal 45.60 g
Mass of Calorimeter 46.60 g
Mass of Water 292.63 g
Initial Temperature of Metal 100 °C
Initial Temperature of Calorimeter 27 °C
Initial Temperature of Water 27 °C
Final Temperature of Mixture 29 °C
Experimental Specific Heat of Metal 0.1835 cal/g*°C
Actual Specific Heat of Metal 0.2174 cal/g*°C
Percentage of Error 15.59 %
Conclusion
Based on the data that we have gathered in the experiment; we can
conclude that the specific heat of the brass metal is quite low and will only
need a few amounts of heat energy to change its temperature by 1°C.
Yielding a result of 15.59% percent error, we were satisfied with the result
for the reason that there are external factor that were inevitable that
affected the percentage error during the experiment, such as room
temperature, the loss of electricity during the experiment which made heat
inconsistent, etc.
Since the specific heat is related to the excitation of the atoms and
how well they hold heat, we can conclude that the experiment is similar to
how a refrigerator function. According to the second law of
thermodynamics heat cannot spontaneously flow from a colder location to
a hotter area. If so then work is required to achieve this. Similarly, a
refrigerator moves heat from inside the cold icebox (the heat source) to the
warmer room-temperature air of the kitchen (the heat sink). The fan pulls
air through the evaporator fins where it is cooled by conduction and
circulated through the refrigerator by forced convection to cool the food.
That heat from the food is transferred into the refrigerant through the tube
walls from the fins by conduction. That heat plus the heat of compression is
rejected by conduction through condenser tubes and fins into the room and
is carried away by natural convection.