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 $de$ in Eqn. \ref{eq:firstlaw:b} using Eqn. \ref{eq:dh}
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:

de=δqδw(Eq. 1)

For a reversible process: δw=pd(1/ρ) and δq=Tds

de=Tdspd(1ρ)(Eq. 2)

Enthalpy is defined as: h=e+p/ρ and thus

dh=de+pd(1ρ)+(1ρ)dp(Eq. 3)

Eliminate de in (Eq. 2) using (Eq. 3)

Tds=dhpd(1ρ)(1ρ)dp+pd(1ρ)(Eq. 2)
ds=dhTdpρT(Eq. 3)

Using dh=CpT and the equation of state p=ρRT, we get

ds=CpdTTRdpp(Eq. 4)

Integrating Eqn. \ref{eq:ds} gives

s2s1=12CpdTTRln(p2p1)(Eq. 5)

For a calorically perfect gas, Cp is constant (not a function of temperature) and can be moved out from the integral and thus

s2s1=Cpln(T2T1)Rln(p2p1)(Eq. 6)

An alternative form of Eqn. \ref{eq:ds:c} is obtained by using de=CvdT Eqn. \ref{eq:firstlaw:b}, which gives

s2s1=12CvdTTRln(ρ2ρ1)(Eq. 7)

Again, for a calorically perfect gas, we get

s2s1=Cvln(T2T1)Rln(ρ2ρ1)(Eq. 8)

Isentropic Relations

Adiabatic and reversible processes, i.e., isentropic processes implies ds=0 and thus Eqn. \ref{eq:ds:c} reduces to

CpRln(T2T1)=ln(p2p1)

CpR=γγ1

γγ1ln(T2T1)=ln(p2p1)

p2p1=(T2T1)γ/(γ1)

In the same way, Eqn. \ref{eq:ds:e} gives

ρ2ρ1=(T2T1)1/(γ1)

Eqn. \ref{eq:isentropic:a} and Eqn. \ref{eq:isentropic:b} constitutes the isentropic relations

p2p1=(ρ2ρ1)γ=(T2T1)γ/(γ1)