Isentropic relations: Difference between revisions
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{{NumEqn|<math>de=\delta q - \delta w</math>|1}} | {{NumEqn|<math>de=\delta q - \delta w</math>|1}} | ||
For a reversible process: <math>\delta w=pd(1/\rho)</math> and <math>\delta q=Tds</math> | For a reversible process: <math>\delta w=pd(1/\rho)</math> and <math>\delta q=Tds</math> | ||
Revision as of 08:42, 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