Isentropic relations: Difference between revisions
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<td style=" | <td style="text-align: center; border: 1px solid blue"><math>de=\delta q - \delta w</math></td> | ||
<td style=" | <td style="width: 5em; padding-right: 0.5em; text-align: right; vertical-align:middle; border: 1px solid blue">(Eq. 1)</td> | ||
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Revision as of 07:54, 27 March 2026
First law of thermodynamics
First law of thermodynamics:
| (Eq. 1) |
For a reversible process: and
Enthalpy is defined as: and thus
Eliminate $de$ in Eqn. \ref{eq:firstlaw:b} using Eqn. \ref{eq:dh}
Using and the equation of state , we get
Integrating Eqn. \ref{eq:ds} gives
For a calorically perfect gas, is constant (not a function of temperature) and can be moved out from the integral and thus
An alternative form of Eqn. \ref{eq:ds:c} is obtained by using Eqn. \ref{eq:firstlaw:b}, which gives
Again, for a calorically perfect gas, we get
Isentropic Relations
Adiabatic and reversible processes, i.e., isentropic processes implies and thus Eqn. \ref{eq:ds:c} reduces to
In the same way, Eqn. \ref{eq:ds:e} gives
Eqn. \ref{eq:isentropic:a} and Eqn. \ref{eq:isentropic:b} constitutes the isentropic relations