Ideal Gas Law Solver — Theory (Kinetic Theory of Ideal Gases)
The ideal gas law connects macroscopic state variables:
\(PV=nRT\).
The same relationship can be written in a molecular form
\(PV = NkT\), where \(N\) is the number of molecules and \(k\) is Boltzmann’s constant.
The bridge between the two views is Avogadro’s constant \(N_A\), where \(N=nN_A\), and \(R=N_Ak\).
1) Macroscopic form
2) Molecular form and kinetic-theory connection
In kinetic theory, pressure arises from molecular collisions with the container walls.
Temperature is proportional to average translational kinetic energy:
\(\langle K \rangle = \tfrac{3}{2}kT\).
3) Density relation
Using \(\rho = m/V\) and molar mass \(M\) (kg/mol), the ideal-gas density is:
The calculator accepts \(M\) in g/mol and converts internally to kg/mol.
4) Partial pressures (mixtures)
For an ideal mixture (Dalton’s law), total pressure is the sum of partial pressures:
\(P_{\text{tot}}=\sum_i P_i\), and
5) University extension: virial correction
Real gases deviate from ideal behavior. A common low-density correction is the second-virial form:
This is an approximation (best at moderate-to-low densities) and depends on temperature through \(B(T)\) in real applications.
6) Avogadro fact (sample input)
At \(P=1\ \text{atm}\) and \(T\approx 273\ \text{K}\), one mole of an ideal gas occupies about \(22.4\ \text{L}\)
(standard molar volume). So if \(P=1\ \text{atm}\), \(V=22.4\ \text{L}\), \(T=273\ \text{K}\), then \(n\approx 1\ \text{mol}\)
and \(N\approx N_A\approx 6.022\times10^{23}\) molecules.