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3.4.2Periodic Table and Energy

Calorimetry

5 min read 5 parts Lesson 11 of 21 Virtual lab

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Part 1 of 5The Calorimetry Equation

3.4.2 Calorimetry

Calorimetry converts a measured temperature change into the enthalpy change of a chemical reaction.

Heat energy
  • q = m c ΔT, where m is the mass of liquid heated in grams, c is the specific heat capacity and ΔT is the temperature change.
Specific heat capacity
  • For water or dilute aqueous solutions, c = 4.18 J g⁻¹ K⁻¹, which is the energy needed to heat 1 g of water by 1 K.
Enthalpy change
  • ΔH = −q ÷ n, with q in kJ and n in moles, where the negative sign shows that a temperature rise means an exothermic reaction.
Mass of solution
  • For aqueous reactions, assume that 1 cm³ of solution has a mass of 1 g, so mass = volume in cm³.

Part 2 of 5Experimental Procedure

1
Measure a known volume of water or solution into a calorimeter such as a polystyrene cup or a metal can, and record its initial temperature.
2
For combustion, weigh a spirit burner containing fuel, light it, and heat the water for a time while stirring.
3
For reactions in solution, add the second reagent, stir constantly and record the highest or lowest temperature reached.
4
Calculate the temperature change, ΔT, and use q = mcΔT to find the heat transferred to the solution.
5
Divide by the moles of the limiting reactant, add the correct sign and express ΔH in kJ mol⁻¹.

Part 3 of 5Errors and Improvements

Errors and Improvements
Heat loss
  • Heat is lost to the surroundings and to the apparatus,
    • so the measured temperature rise is lower and ΔH is less exothermic than the data book value.
Incomplete combustion
  • Soot formation means less energy is released than for complete combustion, so the result is too low.
Insulation
  • Using a polystyrene cup with a lid, and a draught shield for combustion, reduces heat loss.
Extrapolating
  • For solutions, plot temperature against time and extrapolate back to the time of mixing to allow for heat loss.

Part 4 of 5Worked Example

Question

  • 1.15 g of ethanol (M = 46.0 g mol⁻¹) is burned and heats 150 g of water by 25.0 K.
  • Calculate the enthalpy change of combustion of ethanol shown by the data.

  1. q = m c ΔT = 150 × 4.18 × 25.0 = 15 675 J = 15.7 kJ.
    What the symbols mean: E, Q or q = energy transferred (J) · m = mass (kg; g in chemistry calorimetry) · c = specific heat capacity (J kg−1 °C−1; water 4.18 J g−1 °C−1) · ΔT or Δθ = temperature change (°C or K)
  2. n(ethanol) = 1.15 ÷ 46.0 = 0.0250 mol.
  3. ΔH = −15.675 ÷ 0.0250 = −627 kJ mol⁻¹.

Answer ΔcH ≈ −627 kJ mol⁻¹, much less exothermic than the accepted value because of heat losses.

Part 5 of 5Exam Checklist & Tips

3.4.2 – Key Points for the Exam

  • Specific heat capacity The energy required to raise the temperature of 1 g of a substance by 1 K.
  • Calorimeter Apparatus used to measure the heat transferred in a chemical reaction.
  • Enthalpy change of combustion The enthalpy change when 1 mol of a substance burns completely in oxygen under standard conditions.
  • Exothermic A reaction that releases heat and has a negative ΔH.

Common Mistakes

  • Using the mass of the fuel instead of the mass of the water in q = mcΔT.
  • Leaving q in joules when dividing by moles to give kJ mol⁻¹, so the answer is 1000 times too large.
  • Forgetting the negative sign for an exothermic reaction.
  • Using the volume of the total solution but then the moles of the excess reagent instead of the limiting one.
Try it in the virtual labCalorimetry: enthalpy change \n