To determine the final temperature of an ideal gas undergoing adiabatic expansion, we use the adiabatic process relation:
\( TV^{\gamma-1} = \text{constant} \)
For an initial state with temperature \( T_1 = T \) and volume \( V_1 = V \), and a final state with temperature \( T_2 \) and volume \( V_2 = 2V \), the equation becomes:
\( TV^{\gamma-1} = T_2(2V)^{\gamma-1} \)
Simplifying gives:
\( T V^{\gamma-1} = T_2 \cdot 2^{\gamma-1} \cdot V^{\gamma-1} \)
Cancel out \( V^{\gamma-1} \) on both sides:
\( T = T_2 \cdot 2^{\gamma-1} \)
Solve for \( T_2 \):
\( T_2 = \frac{T}{2^{\gamma-1}} \)
Given \( \gamma = \frac{5}{3} \), calculate \( \gamma-1 \):
\( \gamma-1 = \frac{5}{3} - 1 = \frac{2}{3} \)
Substitute back to find \( T_2 \):
\( T_2 = \frac{T}{2^{2/3}} \)
The final temperature \( T_2 \) is \( \frac{T}{2^{2/3}} \).
An ideal monatomic gas of $ n $ moles is taken through a cycle $ WXYZW $ consisting of consecutive adiabatic and isobaric quasi-static processes, as shown in the schematic $ V-T $ diagram. The volume of the gas at $ W, X $ and $ Y $ points are, $ 64 \, \text{cm}^3 $, $ 125 \, \text{cm}^3 $ and $ 250 \, \text{cm}^3 $, respectively. If the absolute temperature of the gas $ T_W $ at the point $ W $ is such that $ n R T_W = 1 \, J $ ($ R $ is the universal gas constant), then the amount of heat absorbed (in J) by the gas along the path $ XY $ is