Isentropic relations: Difference between revisions
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{{NumEqn|<math> | {{NumEqn|<math> | ||
de=Tds-pd\left(\frac{1}{\rho}\right) | de=Tds-pd\left(\frac{1}{\rho}\right) | ||
</math>|2}} | </math>|eq-first-law-b|2}} | ||
Enthalpy is defined as: <math>h=e+p/\rho</math> and thus | Enthalpy is defined as: <math>h=e+p/\rho</math> and thus | ||
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{{NumEqn|<math> | {{NumEqn|<math> | ||
dh=de+pd\left(\frac{1}{\rho}\right)+\left(\frac{1}{\rho}\right)dp | dh=de+pd\left(\frac{1}{\rho}\right)+\left(\frac{1}{\rho}\right)dp | ||
</math>|3}} | </math>|eq-dh|3}} | ||
Eliminate | Eliminate <math>de</math> in {{EquationNote|eq-first-law-b}} using {{EquationNote|eq-dh}} | ||
{{NumEqn|<math> | {{NumEqn|<math> | ||
Revision as of 18:13, 28 March 2026
First law of thermodynamics
First law of thermodynamics:
| (Eq. 1) |
For a reversible process: and
| (Eq. 2) |
Enthalpy is defined as: and thus
| (Eq. 3) |
Eliminate in (Eq. 2) using (Eq. 3)
| (Eq. 2) |
| (Eq. 3) |
Using and the equation of state , we get
| (Eq. 4) |
Integrating Eqn. \ref{eq:ds} gives
| (Eq. 5) |
For a calorically perfect gas, is constant (not a function of temperature) and can be moved out from the integral and thus
| (Eq. 6) |
An alternative form of Eqn. \ref{eq:ds:c} is obtained by using Eqn. \ref{eq:firstlaw:b}, which gives
| (Eq. 7) |
Again, for a calorically perfect gas, we get
| (Eq. 8) |
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