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Thermodynamics

The Ideal Gas Law

\[ pV=nRT=Nk_BT,p=\dfrac{\rho k_BT}{m},U=\alpha nRT \]

where:

  • \(p\) is the absolute pressure of the gas,
  • \(V\) is the volume of the gas,
  • \(n\) is the number of moles,
  • \(R\) is the ideal gas constant,
  • \(k_B\) is the Boltzmann constant,
  • \(N_A\) is the Avogadro constant,
  • \(T\) is the absolute temperature of the gas,
  • \(\alpha\) is the number of degrees of freedom divided by \(2\). (\(\alpha = 3/2\) for monatomic gas, \(\alpha = 5/2\) for diatomic gas).
  • \(N\) is the number of particles.

Van der Waals equation

\[ (p+\dfrac{a}{V^2})(V-b)=RT,p=\dfrac{RT}{V-b}-\dfrac{a}{V^2} \]

The First Law of Thermodynamics

\[ dU= dW +dQ,dW=-pdV \]

The Second Law of Thermodynamics

\[ dS=\dfrac{dQ}{T} \]

Adiabatic Process

\[pV^\gamma = \text{constant}\]
\[p^{1-\gamma}T^\gamma = \text{constant}\]
\[TV^{\gamma - 1}=\text{constant}\]

where \(\gamma\) is the adiabatic index or heat capacity ratio defined as:

\[ \gamma=\dfrac{C_p}{C_V} = \dfrac{f+2}{f} \]
  • \(C_p,C_V\) is the specific heat for constant pressure, \(C_V\) is the specific heat for constant volume, and \(f\) is the number of degrees of freedom (3 for monoatomic gas, 5 for diatomic gas or a gas of linear molecules).

Derivation for P-V relation:

The adiabatic process is defined as a process where heat transfer is zero, then we can apply the first law of thermodynamics:

\[ dQ=dU-dW=d(\alpha pV)+pdV=(\alpha +1)pdV+\alpha Vdp=0 \]

We can separate the variable:

\[ -(\alpha + 1)\dfrac{dV}V=\alpha\dfrac{dp}p \]

Integrate on both sides:

\[ \ln(p/p_0)=-\dfrac{\alpha + 1}{\alpha}(V/V_0) \]

And then exponentiate them, substituting \(\gamma=\dfrac{\alpha + 1}{\alpha}\) .

Similar derivations can be done for Van der Waals equation.

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