6.3 - Standard Enthalpy Change of Neutralisation
- 1Standard enthalpy change of neutralisation
- 2Solution calorimetry
- 3Creating an accurate temperature-time graph
- 4Calculating standard enthalpy change of neutralisation
Standard enthalpy change of neutralisation
The standard enthalpy change of neutralisation (ΔH⦵neut) is the enthalpy change when an acid and alkali neutralise under standard conditions to form one mole of water. Neutralisation is exothermic so ΔH⦵neut values are always negative.
For example, the equation representing the standard enthalpy change of neutralisation of hydrochloric acid (HCl) is:
HCl(aq) + NaOH(aq) ➔ NaCl(aq) + H2O(l) ΔH⦵neut = 57 kJ mol-1.
Solution calorimetry

Solution calorimetry can find enthalpy changes for reactions occurring in aqueous solutions, including:
- Neutralisation
- Dissolution
- Displacement
The steps are:
- Add a measured volume of one reactant to a polystyrene cup calorimeter and record initial temperature.
- Add a measured volume of a second reactant and quickly seal the container with a lid.
- Carefully stir the mixture with the thermometer and record temperatures at regular intervals over time as heat is released or absorbed.
Polystyrene cups are used as the calorimeter for solution calorimetry instead of glass beakers because polystyrene is a better insulator, lightweight, waterproof, and has a low specific heat capacity. These properties reduce heat loss to the surroundings and minimise the amount of heat absorbed by the calorimeter itself.
Creating an accurate temperature-time graph
During a calorimetry experiment, the temperature fluctuates throughout - increasing rapidly as heat is released, reaching a peak, then decreasing gradually again.
If we just subtracted the final and initial values, we would underestimate the temperature change by missing the peak and not accounting for heat lost while measuring.
To accurately determine the temperature change:

- Plot the data - Begin by plotting the recorded temperature against time.
- Establish baseline - Draw a line of best fit for the initial temperature readings before the reaction commences. This is your baseline.
- Post-reaction line - After the peak reaction temperature is reached, draw another line of best fit for the cooling period.
- Extrapolation - Extend both lines to intersect at the reaction's start time.
- True temperature change - The difference between the two extrapolated lines of best fit at the start of the reaction gives the accurate temperature change.
Calculating enthalpy change of neutralisation
To measure the enthalpy change of neutralisation, you need to use two key equations sequentially: first to calculate the heat energy change, and then to use that value to calculate the enthalpy change per mole.
First, the heat energy change can be calculated using the equation:
q = mcΔT
Where:
- q = heat energy (J)
- m = mass of solution (g)
- c = specific heat capacity of water, 4.18 J g^-1^ K^-1^
- ΔT = temperature change (K) The official unit for ΔT is Kelvin (K). However, the Celsius scale gives the same numerical temperature change, so °C can also be used.
Next, use the value of q obtained from the first equation to find the enthalpy change with the equation:
Where:
- ΔHneut = enthalpy change of neutralisation (kJ mol-1)
- q = heat energy (kJ)
- n = number of moles of the limiting reactant (mol) Enthalpy changes are typically expressed in kJ mol-1 so you need to convert q from J to kJ by dividing by 1,000 before using it in the second equation.
Worked example 1 - Calculating standard enthalpy of neutralisation
In a laboratory experiment, 50.0 cm3 of 1.00 mol dm-3 hydrochloric acid (HCl) at 25.0°C is mixed with 50.0 cm3 of 1.00 mol dm-3 sodium hydroxide solution (NaOH) also at 25.0°C. The heat formed during this neutralisation raised the temperature of the mixture to 31.5°C.
Calculate the standard enthalpy of neutralisation (ΔH⦵neut) of hydrochloric acid.
The specific heat capacity of the mixture, c = 4.18 J g-1 K-1.
The density of the mixture, ρ = 1.00 g cm-3
Step 1: Calculate heat energy transferred
q = mcΔT = (50.0 + 50.0) x 4.18 x (31.5 - 25.0) = 2,717 J
Step 2: Conversion of J into kJ
To convert from J into kJ, divide by 1,000
2,717 J = 2.717 kJ
Step 3: Conversion of cm3 into dm3
To convert from cm3 into dm3, divide by 1,000
50.0 cm3 = 0.0500 dm3
Step 4: Calculate number of moles of HCl used
n = c x V = 1.00 x 0.0500 = 0.0500 mol
Step 5: Calculate heat released per mole of HCl
The minus sign indicates this is an exothermic reaction, releasing heat.