CH1401 Thermodynamics Lecture 3
Overview of Thermodynamics Concepts
1. Energy and Work
Energy can be identified in forms such as work (W) and heat (q), influencing thermodynamic processes.
Final and initial energy values are significant in determining the change in energy in a system.
2. Heat (q)
2.1 Definition
Heat refers to the energy transferred to or from a system due to a temperature difference.
2.2 Temperature-Heat Relationship
For an ideal gas, temperature increase is proportional to the heat supplied.
Heat capacity (C) characterizes this relationship as: C = q/ delta T
Units: J K⁻¹
Values vary for different phases of water: ice, liquid, steam.
2.3 Latent Heat
Temperature change may not occur during phase changes, where latent heat is absorbed.
3. Heat Capacity
3.1 Types
Extensive Property: Depends on the amount of substance.
Intensive Property: Independent of the amount of substance.
Specific Heat Capacity (Cs):[ C_s = \frac{q}{m \Delta T} ]
Units: J K⁻¹ g⁻¹
Molar Heat Capacity (Cm):[ C_m = \frac{q}{n \Delta T} ]
Units: J K⁻¹ mol⁻¹
3.2 Worked Example
Calculate energy to raise the temperature of 2 moles of liquid benzene by 20 K using tabulated values for Cs and Cm.
4. Internal Energy (U)
4.1 Definition
U accounts for all kinetic and potential energy in a system, comprising contributions from atomic, ionic, and molecular motions.
4.2 Change in Internal Energy
The formula is given by:[ \Delta U = q + w ]
Where: q = heat added, w = work done on/by the system.
4.3 Path Dependency
Change in internal energy is a state function, implying it only depends on initial and final states, not the path taken.
5. First Law of Thermodynamics
States that internal energy in an isolated system remains constant; reinforces energy conservation.
Energy changes (q and w) should sum to zero for a closed system.
6. Enthalpy (H)
6.1 Definition
Enthalpy accounts for heat changes at constant pressure:[ H = U + pV ]
6.2 Enthalpy Change
Given by:[ \Delta H = \Delta U + p \Delta V ]
Heat transfer under constant pressure is equal to change in enthalpy.
6.3 Exothermic vs Endothermic Reactions
Exothermic (q < 0) = Release of heat, decrease in enthalpy.
Endothermic (q > 0) = Absorption of heat, increase in enthalpy.
7. Calculations and Examples
Calculating heat capacity from calorimetry data.
Application of heat transfer equations in phase transitions and state changes.
8. Self-test Questions
Focus on calculations involving specific heat capacity and internal energy change.
Example questions provide practical engagement with thermodynamic principles.
9. Review Points
Understand concepts of heat capacity, specific and molar heat capacities.
Internal energy as a state function and its implications in thermodynamic processes.
Grasp the first law of thermodynamics and enthalpy definitions and applications.