A model for the electron-vibration energy exchange in nitrogen based on a Landau-Teller-type rate equation is presented. Analytical expressions of relaxation times are derived for cutoff harmonic oscillator and Morse oscillator approximations, assuming that the relaxation proceeds by way of a continuous series of Boltzmann distributions over the vibrational states. Comparisons with the direct numerical integration of the master equation have shown that the use of a two-temperature relaxation time allows accurate modeling of the nitrogen vibrational energy relaxation rate for various conditions encountered in high-enthalpy ows with electron and vibrational temperatures up to 40,000 K. Nomenclature a = constant in the analytical expression of rate coef cients for v > 0 ! w > v transitions dE n v / dt = nondimensionalvibrational energy relaxation rate E v = vibrational energy per unit volume, J/m 3 E ¤ v = vibrational energy calculated with vibrational levels in Boltzmann equilibrium at the electron temperature T e , J/m 3 E v, init = vibrational energy at 0-s time, J/m 3 J = rotational quantum number k B = Boltzmann constant, J/K k v,w = electron-vibration(E-V) rate coef cient of the v ! w transition, m 3 /s N t = total N 2 number density, N v , m ¡ 3 N v = number density of the vibrational level v of N 2 , m ¡ 3 n e = electron number density, m ¡ 3 p e = electron partial pressure, n e k B T e , atm T e = electron temperature, K T v , T exci = vibrational temperature, K t = time, s t n = nondimensionaltime v m = total number of excited vibrational levels D ² = constant of the Morse oscillator, cm ¡ 1 ²(v) = energy of the vibrational level v of N 2 , J ² 1 = energy of the rst vibrational level of N 2 , J r v, w = E-V cross section of the v ! w transition, m 2 s e = E-V relaxation time, s Supercripts HO = truncated harmonic oscillator MO = Morse oscillator