Enthalpy of Phase Transition — Core Principles
Core Principles
Enthalpy of phase transition, also known as latent heat, is the energy absorbed or released when a substance changes its physical state (solid, liquid, gas) at constant temperature and pressure. This energy is used to overcome or establish intermolecular forces, not to change the kinetic energy of particles, hence the constant temperature.
Key transitions include fusion (melting, solid to liquid, ), vaporization (boiling, liquid to gas, ), and sublimation (solid to gas, ). Their reverse processes (freezing, condensation, deposition) are exothermic, having negative enthalpy values.
The magnitude of these enthalpy changes is primarily determined by the strength of intermolecular forces. Hess's Law relates these, stating . These concepts are vital for understanding energy changes in various natural and industrial processes, and for solving numerical problems in NEET that often combine specific heat calculations with phase change enthalpies.
Important Differences
vs Specific Heat Capacity
| Aspect | This Topic | Specific Heat Capacity |
|---|---|---|
| Definition | Enthalpy of Phase Transition (Latent Heat) | Specific Heat Capacity |
| What it measures | Heat absorbed/released during a phase change at constant temperature. | Heat absorbed/released to change the temperature of a substance without a phase change. |
| Temperature change | No temperature change occurs during the process. | Always involves a change in temperature. |
| Units (common) | Joules per mole (J/mol) or Joules per gram (J/g). | Joules per gram per Kelvin (J/g·K) or Joules per mole per Kelvin (J/mol·K). |
| Energy utilization | Energy used to overcome/establish intermolecular forces. | Energy used to increase/decrease the kinetic energy of particles. |
| Formula (for calculation) | $q = n cdot Delta H_{transition}$ (or $q = m cdot L$) | $q = m cdot c cdot Delta T$ |