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Lecture 2 Practice: Heat and Enthalpy in Biopharmaceutical Processes
Equation sheet
- q = m × C × ΔT (C in J g−1 K−1: m in g, q in J)
- Energy = power × time; 1 W = 1 J s−1
- Mixing: heat gained by the cold liquid = heat lost by the hot liquid
- n = m / M
- ΔrH° = ΣnΔfH°(products) − ΣmΔfH°(reactants)
- Change of state: q = n × ΔvapH (per mole) or q = m × latent heat (per gram)
- ΔH < 0: exothermic (heat released); ΔH > 0: endothermic (heat absorbed)
- A change of 1 °C = a change of 1 K; 1 kJ = 1,000 J; 1 h = 3,600 s
Key terms, if this is new to you
- System and surroundings
- The system is what we are studying (a dissolving salt, a batch of medium). The surroundings are everything else.
- Heat and temperature
- Heat, q, is energy transferred because of a temperature difference. Temperature measures how hot something is.
- Specific heat capacity, C
- The heat needed to warm 1 g of a substance by 1 K. Water's is high: 4.18 J g−1 K−1.
- Enthalpy change, ΔH
- The heat taken in or given out by a process at constant pressure. Negative: heat out (exothermic). Positive: heat in (endothermic).
- Latent heat and ΔvapH
- The heat needed to change state (melt, boil, sublime) without any change in temperature.
- Standard enthalpy of formation, ΔfH°
- ΔH for making one mole of a substance from its elements. Elements such as O2(g) have ΔfH° = 0.