First law
Energy is conserved. Heat Q added to a closed system either raises its internal energy U or leaves as work W done by the system:
ΔU = Q − W
- U
- internal energy
- J
- Q
- heat added to the system
- J
- W
- work done by the system
- J
- n
- amount of gas
- mol
- cv
- molar heat capacity, constant volume
- J/(mol·K)
- cp
- molar heat capacity, constant pressure
- J/(mol·K)
- R
- molar gas constant, 8.314
- J/(mol·K)
- T
- temperature
- K
- p
- pressure
- Pa
- V
- volume
- m³
| ΔT | 172 K |
| W | 1.43 kJ |
| ΔU = Q − W | 3.57 kJ |
Worked example
Uses the values in Fig. 1.2-1. Change them and the working updates.
Given
- Qheat added5 kJ
- namount of gas1 mol
- cvdiatomic gas (air, N₂, O₂)2.5R
- processconstant pressure
Find
The change in internal energy ΔU.
Solution
c = cₚ = cᵥ + R = 29.1 J/(mol·K)
ΔT = Q/nc = 5,000 J / (1 mol × 29.1 J/(mol·K)) = 172 K
W = nRΔT = 1 mol × 8.314 J/(mol·K) × 172 K = 1.43 kJ
ΔU = Q − W = 5 kJ − 1.43 kJ = 3.57 kJ
Answer
ΔU = 3.57 kJ
71.4% of the heat went into internal energy, raising the temperature by 172 K.
Related cases
-
Isothermal, ideal gas
ΔU = 0Q = W = nRT ln(V2V1)
-
Adiabatic, no heat
Q = 0ΔU = −W
-
Complete cycle
ΔU = 0Qnet = Wnet
Assumptions
- The system is closed: no mass crosses its boundary.
- Heat into the system and work done by it are positive. Some texts count work done on the system instead and write ΔU = Q + W.
- The gas is ideal with constant heat capacities, so U depends on temperature alone.
- The process is slow enough that the gas is always close to equilibrium.
- Changes in the system's bulk kinetic and potential energy are ignored.
Derivation
- Energy is conserved, so heat in either stays in the gas or leaves as work:
Q = ΔU + W. - For an ideal gas, U depends only on temperature:
ΔU = ncvΔT. - At constant pressure the gas pushes its boundary out:
W = p ΔV = nR ΔT. - So
Q = n(cv + R)ΔT = ncpΔT, which gives ΔT from Q.
At constant volume no work is done, so all of the heat raises U: Q = ncvΔT.