Rayleigh scattering#
Scattering of light by molecules is well modeled using the Rayleigh approximation (see [Liou, 2002], section 3.3.1 for example).
Phase function#
We use the phase function \([/]\) (units: \(\mathrm{str}^{-1}\)) expression provided by [Hansen and Travis, 1974] (eq. 2.14):
where
\(\theta\) is the scattering angle \([/]\) (units: \(\mathrm{rad}\)) and
\(\Delta\) \([/]\) is given by:
where \(\delta\) is the depolarisation factor \([/]\).
We take \(\delta = 0\) for air, which gives \(\Delta = 1\).
Warning
We use the following normalisation rule for the phase function:
where \(\phi\) is the azimuth angle \([/]\) (units: \(\mathrm{rad}\)).
Scattering coefficient#
We use the expression of the scattering coefficient \([L^{-1}]\) for a pure gas provided by [Eberhard, 2010] (eq. 60), and apply it to air:
where
\(\lambda\) is the wavelength \([L]\) (subscript indicates spectral dependence),
\(n\) is the air number density \([L^{-3}]\),
\(\eta\) is the air refractive index \([/]\) and
\(F_{\lambda}\) is the air King correction factor \([/]\).
Note
Since air is considered as a pure gas, variations of the scattering coefficient with composition are neglected.
The spectral dependence of the air refractive index is computed according to [Peck and Reeder, 1972] (eq. 2), valid in the wavelength range \([230, 1690]\) nm. In the wavelength range [1690, 2400] nm, we assume that this equation remains accurate enough, although we have no data to justify that assumption.
The number density dependence is computed using the simple proportionality rule:
where
\(n_0\) is the air number density under standard conditions of pressure and temperature (101325 Pa, 288.15 K) and
\(\eta_0\) is the air refractive index under standard conditions of pressure and temperature.
The King correction factor is computed using the data from [Bates, 1984] (table 1). The data is interpolated within the [200, 1000] nm range and extrapolated using the 1000 nm value for wavelength larger than 1000 nm.