“…f ←i (T ). Following Baranger [17], Schaefer & Monchik [20,21] and Green [22], we have, for a rotational transition of H 2 O (j f , τ f ← j i , τ i ), assuming that H 2 remains in an unchanged j 2 state:…”
Theoretical cross sections for the pressure broadening by hydrogen of rotational transitions of water are compared to the latest available measurements in the temperature range 65-220 K. A high-accuracy interaction potential is employed in a full close-coupling calculation. A good agreement with experiment is observed above ∼80 K, while the sharp drop observed experimentally at lower temperatures is not predicted by our calculations. Possible explanations for this discrepancy include the failure of the impact approximation and the possible role of ortho-to-para conversion of H 2 .
“…f ←i (T ). Following Baranger [17], Schaefer & Monchik [20,21] and Green [22], we have, for a rotational transition of H 2 O (j f , τ f ← j i , τ i ), assuming that H 2 remains in an unchanged j 2 state:…”
Theoretical cross sections for the pressure broadening by hydrogen of rotational transitions of water are compared to the latest available measurements in the temperature range 65-220 K. A high-accuracy interaction potential is employed in a full close-coupling calculation. A good agreement with experiment is observed above ∼80 K, while the sharp drop observed experimentally at lower temperatures is not predicted by our calculations. Possible explanations for this discrepancy include the failure of the impact approximation and the possible role of ortho-to-para conversion of H 2 .
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