What Is Molar Heat Capacity And How Do You Calculate It?

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Molar heat capacity is the amount of heat required to raise the temperature of 1 mole of a substance by 1 unit & is calculated by dividing heat capacity by the total number of moles.

Have you ever wondered why we don’t burn ourselves while using a pan?

Of course, it is the handle that protects us, but why doesn’t it get as hot as the pan itself? After all, it is exposed to the same amount of heat.

For starters, a panhandle is typically plastic, which means that it is a poor conductor of heat. Also, given the same amount of heat exposure, the rise in the temperature of the plastic handle is much less than that of the metal portion. This is attributed to the handle’s high heat capacity compared to the metal the pan is made from.

Heat capacity is defined as the amount of heat energy required to raise the temperature of a given mass of a substance by one unit. Specific heat capacity and molar heat capacity are properties derived from the heat capacity of a material.

Heat capacity
Owing to the high heat capacity of the handle, it doesn’t get as hot as the pan itself (Photo Credit: Kzenon/Shutterstock).

Specific Heat & Molar Specific Heat

Heat capacity is an extensive property, i.e., it depends on the amount and size of the substance. A modified form of heat capacity (called specific heat capacity or simply specific heat) is commonly used in physics. Specific heat doesn’t vary with the amount of the substance and is, therefore, a more useful property.

Specific heat is defined as the amount of heat required to raise one unit of mass of the substance by 1 unit of temperature. Mathematically, it is the heat capacity of a substance divided by its mass. The formula for specific heat is:

c = C/m

Here, c is specific heat and has units J/kg.K, C is the heat capacity of a substance in J/K, and m is the mass of the substance in kilograms. Another very important formula used to express specific heat is:

c = ΔQ/(m · ΔT)

Here, too, c stands for specific heat, ΔQ is the difference in heat energy in joules, m is the mass of the substance, and ΔT is the difference in temperature in Kelvin.

In chemistry (where the amount of a substance is usually measured in moles, not grams), further modifying the definition and formula of heat capacity to include moles makes things a lot easier.

Molar heat capacity is defined as the amount of heat required to raise 1 mole of a substance by 1 Kelvin. Like specific heat, molar heat capacity is an intensive property, i.e., it doesn’t vary with the amount of substance.

Mathematically, it is the heat capacity of a substance divided by the number of moles and is expressed as:

cm = C/n

Here, cm is molar heat capacity (J/K.mol), C is heat capacity (J/K), and n is the number of moles (mol).

Specific heat and molar heat capacity may not vary with the amount or size of the substance, but their values fluctuate based on the method of determination.

When heat energy is supplied to a substance, particularly gases, the temperature rise is accompanied by an increase in either volume or pressure, and sometimes both. These phenomena are explained by Charles’ law and Gay-Lussac’s law.

CP,m & CV,m are often used to represent molar heat capacities measured at constant pressure (isobaric) and constant volume (isochoric).

The value of molar specific heat at constant pressure is always greater than that measured at constant volume. This is because heat supplied at constant pressure is used to produce work and also expand in volume. In contrast, heat supplied at constant volume is entirely utilized to increase the temperature of the substance.

The ratio of CP and CV is called the heat capacity ratio or adiabatic index (γ = CP/CV), and is an important term when working with reversible processes in thermodynamics. For an ideal gas, the difference between CP,m and CV,m equals the universal gas constant R. The expression CP,m − CV,m = R is called Mayer's relation, and it holds strictly only for ideal gases (real gases follow it only approximately, and at low pressures).

How To Calculate The Molar Heat Capacity Of A Substance?

Determining a substance’s heat capacity and subsequently its specific heat and molar heat capacity is not exactly rocket science. The values can be calculated by simply breaking down their definitions, finding individual quantities (amount of heat supplied or removed, initial temperature, final temperature, the mass, and the number of moles of the substance), and substituting them in their respective places in the formulas.

Step 1: Finding Heat Capacity

As already defined, heat capacity is the amount of heat required to raise the temperature of a known quantity of the substance by one unit. The definition is expressed as:

C = QT

Here, C is heat capacity, Q represents heat energy, and ΔT is the temperature difference. ΔQ can also replace Q.

ΔT is T2 − T1, where T1 is the initial temperature and T2 is the final temperature of the substance (so ΔT is positive when the substance is heated). Begin by noting down the initial/starting temperature T1 using a thermometer. Also, weigh the sample (m) and note the value in kg for later use.

Next, supply a known quantity of heat energy (Q) to the system. The quantity of heat energy can be noted in either joules or calories. Once you’re done supplying heat, wait for the temperature to stabilize and note the final temperature as T2.

Convert the temperature value to Kelvin by adding the number 273.15 to the Celsius value (0°C = 273.15 K). If the value of heat energy supplied is available in calories, convert it to joules. Multiply the amount of heat energy in calories by 4.184 to get the amount in joules (1 cal = 4.184 joules).

Finally, substitute the values of Q, T1, and T2 in the heat capacity formula. Grab a calculator or use your brain to perform the calculations and obtain the sample’s heat capacity. The units of heat capacity are J/K.

Step 2: Finding Specific Heat Capacity Or Specific Heat

Specific heat capacity or specific heat can easily be found by dividing the sample’s heat capacity by its mass (c = C/m). Go ahead and divide the value of C found in the previous step by the value of m, also noted in the previous step, to obtain the specific heat of the sample. The resulting quantity will have the units J/kg.K

Step 3: Determining Molar Heat Capacity

If you scroll back up and look at the formula for molar heat capacity (cm= C/n), you will find the term ‘n’, representing the number of moles of the sample. To find the number of moles, divide the quantity of the sample by its molar mass.

no of moles formula
n = m/M

Now that you have found n, substitute the value of heat capacity (C) and the number of moles (n) in the formula and calculate molar heat capacity.

Another method for determining molar heat capacity is multiplying the specific heat (c) of the sample by its molar mass (M). When doing this, be sure to convert the molar mass to kg/mol.

molar heat capacity formula

Alternative Method – Using A Calorimeter

Another method for determining the specific heat of a substance is the use of a calorimeter. A calorimeter is a scientific apparatus consisting of the following parts: an inner and outer vessel, stirrer, thermometer, insulating material, etc.

The inner vessel or cup contains the sample material whose specific heat is to be determined. It is placed in the middle of the outer vessel which is filled with water.

The procedure starts by noting the mass and initial temperatures of both the water and the sample substance.

calorimeter
The calorimeter is used to measure the heat flow in a reaction; this technique is called calorimetry. (Photo Credit: Fouad A. Saad/Shutterstock)

The sample is then heated using ignition wires. As the temperature of the sample rises above the temperature of the outside water, heat transfer between the two begins. After some amount of time, the electric flow is turned off, and the final temperatures of the water and the sample are measured. The heat energy lost by the sample material will be equal to the heat gained by the water in the outside vessel. We now make use of the formula ΔQ = mcΔT.

For the sample, ΔQs= (mcΔT)s, and for the water, ΔQw=(mcΔT)w.

But ΔQ= ΔQw. Thus, (mcΔT)= (mcΔT)w.

Substitute the values for the mass of the sample and the water (ms and mw, respectively), the change in temperature (ΔTs = T1s-T2s and ΔTw = T1w-T2w), and the specific heat of water (cw) as 4.186 kJ/kg.K to determine the specific heat of the sample (cs). Once the substance’s specific heat is found, multiplying it by its molar mass will provide you with the molar heat capacity of the substance.

Molar Heat Capacity Of Gases: CP, CV And Degrees Of Freedom

Gases are the one case where you cannot quote a single molar heat capacity and be done with it. As mentioned earlier, a gas can absorb heat either at constant volume (CV,m) or at constant pressure (CP,m), and the two values are genuinely different. At constant volume, every joule of heat goes into raising the temperature. At constant pressure the gas also expands and does work on its surroundings, so it needs extra heat to reach the same temperature. That is why CP,m is always larger, and for an ideal gas the gap is exactly the gas constant R (Mayer's relation, CP,m = CV,m + R).

Degrees of freedom of a diatomic molecule: three translational, two rotational, and vibrational motions that store thermal energy
(Photo Credit: Wikimedia Commons, Public domain)

The actual size of these values comes from a beautifully simple idea: the equipartition of energy. Each independent way a molecule can store energy (called a degree of freedom) holds an average of half of R per mole. A single atom of a monatomic gas, such as helium or argon, can only move along three directions in space, giving three translational degrees of freedom. That works out to CV,m = 3/2 R, roughly 12.5 J/(mol·K), and CP,m = 5/2 R, roughly 20.8 J/(mol·K).

A diatomic molecule like nitrogen or oxygen can also tumble end over end, adding two rotational degrees of freedom for a total of five at room temperature. That raises the values to CV,m = 5/2 R, roughly 20.8 J/(mol·K), and CP,m = 7/2 R, roughly 29.1 J/(mol·K). This is exactly why a problem that tells you a gas has CP,m = 7/2 R is quietly telling you the gas is diatomic. The ratio γ = CP/CV follows directly too: about 1.67 (5/3) for a monatomic gas and 1.40 (7/5) for a diatomic one, which is the value engineers use for air.

The vibrational motion shown in the diagram (the two atoms stretching along their bond) is a further set of degrees of freedom, but it only starts absorbing significant energy at high temperatures. That temperature dependence, invisible in the simple ideal-gas formula, is an early hint of the quantum behavior of heat capacity.

What Are The Molar Heat Capacity Values Of Common Substances?

Once you know how to calculate molar heat capacity, it helps to have a feel for the numbers themselves. The table below lists the molar heat capacity of some everyday substances measured near room temperature (25°C) and expressed in joules per kelvin per mole, J/(mol·K), which is the SI unit for this quantity.

SubstanceMolar heat capacity (J/(mol·K))
Water (liquid)75.3
Ice (0°C)38.1
Air (dry)29.2
Lead26.4
Gold25.4
Selenium25.4
Iron25.1
Silver24.9
Copper24.5
Aluminium24.2

One pattern jumps out immediately: almost every solid metallic element sits close to 25 J/(mol·K), whether it is light aluminium or heavy lead. This is not a coincidence. In 1819, French scientists Pierre Louis Dulong and Alexis Thérèse Petit noticed that the molar heat capacity of most solid elements is roughly 3R, or about 25 J/(mol·K), a result now called the Dulong–Petit law. It is why a query such as the molar heat capacity of selenium at standard conditions returns about 25.4 J/(mol·K): selenium is simply another solid element obeying the same rule.

The reason again comes down to degrees of freedom. Each atom locked into a crystal lattice can vibrate in three directions, and each vibration carries both kinetic and potential energy, giving six half-R contributions that add up to 3R per mole. The law breaks down in two situations: at very low temperatures, where quantum effects freeze out those vibrations and the heat capacity falls toward zero, and for light, tightly bonded elements such as carbon in diamond, whose molar heat capacity at room temperature is far below 25 J/(mol·K). Liquid water stands apart at 75.3 J/(mol·K) because a water molecule has many more ways to store energy than a single atom pinned in a lattice.

Applications Of Heat Capacity

The heat capacity of a substance determines where and when it can be used. For example, the handles and bodies of utensils are manufactured from materials with a high heat capacity to ensure the user’s safety. On the other hand, thermometers are manufactured from materials with a low specific heat capacity to detect even the smallest temperature fluctuations.

Another example of this is the use of water in engine cooling systems. Water has one of the highest specific heat capacities of any common liquid (about 4.18 kJ/(kg·K)), beaten in liquid form only by a few specialized substances like liquid ammonia. For the same amount of heat, the rise in water temperature is minimal, making it an ideal choice for a cooling liquid/agent.

The phenomenon of seawater remaining cooler than the surrounding air and sand on a hot summer day, even though it is exposed to the same amount of heat from the sun, can also be explained by the concept of heat capacity: the high heat capacity of water is responsible for many natural events, including the Earth’s climate and the survival of aquatic life!


References (click to expand)
  1. USGS.gov | Science for a changing world. The United States Geological Survey
  2. Physics 23 Fall 1993Lab 2 - Adiabatic Processes - www.dartmouth.edu:80
  3. Heat Capacity - Thermodynamics. The University of Wisconsin–Madison
  4. Specific Heat Capacity and Water | U.S. Geological Survey. The United States Geological Survey
  5. Molar heat capacity - Wikipedia
  6. Specific Heats of Gases - HyperPhysics, Georgia State University
  7. Dulong–Petit law - Wikipedia