Abstract
A theoretical model based on the energy corrected sudden (ECS) approximation is used in order to account for line-mixing effects in Δ ↔ Π infraredQbranches of12C16O2. Its quality is demonstrated by comparisons with numerous laboratory spectra of CO2–He and CO2–N2mixtures: threeQbranches in the 4 and 17 μm regions are investigated at room temperature in a wide pressure range. The influence of mixing betweenQ(J) lines associated with odd and even values of the rotational quantum numberJis demonstrated and analyzed in detail. It is shown that, in contrast to available fitting law approaches, the ECS model correctly predicts the influence of the parity of the rotational quantum numbersJandJ′ on coupling between theQ(J) andQ(J′) lines. Comparisons between the effects of collisions of CO2with N2and He are made and analyzed. They show that these two systems involve different line couplings within theQbranch.
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