Absorption profiles of HCl for the J=1–0 rotational transition: Foreign-gas effects measured for N2, O2, and Ar

Morino, Isamu; Yamada, Kōichi

doi:10.1016/j.jms.2005.06.003

Cited by 17 publications

(7 citation statements)

References 31 publications

(56 reference statements)

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“…The narrowing parameter is fixed to the b 0 diff value equal to 20.7 Â 10 À3 cm À1 atm À1 . The q parameter is fixed equal to 6. recently pointed out for broadening and shifting of the R(0) rotational transition [40].…”

Section: Resultsmentioning

confidence: 92%

Narrowing broadening and shifting parameters for R(2) and P(14) lines in the HCl fundamental band perturbed by N2 and rare gases from tunable diode laser spectroscopy

Hurtmans

Henry

Valentin

et al. 2009

Journal of Molecular Spectroscopy

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Section: Resultsmentioning

confidence: 92%

Narrowing broadening and shifting parameters for R(2) and P(14) lines in the HCl fundamental band perturbed by N2 and rare gases from tunable diode laser spectroscopy

Hurtmans

Henry

Valentin

et al. 2009

Journal of Molecular Spectroscopy

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“…The reference values were obtained from the HITRAN database [1] and associated literature. [2,[13][14][15][16][17][18][19][20][21][22] A total of 28 transition frequencies spanning v = 0 − 3 and J = 0 − 4 were used in the present analysis. .…”

Section: S2 Design Of Bond Functionmentioning

confidence: 99%

“…Comparison between the reference values and the calculated results for the ro-vibrational transition frequencies (in cm −1 ) of HCl molecule. The reference values were obtained from the HITRAN database[1] and associated literature [2,[13][14][15][16][17][18][19][20][21][22]. A total of 28 transition frequencies spanning v = 0 − 3 and J = 0 − 4 were used in the present analysis.…”

mentioning

confidence: 99%

Testing the limitations of harmonic approximation in the determination of Raman intensities

2022

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T2 Polarizability components (α ⊥ and α ∥ ) and invariants (ᾱ and γ) of HF calculated with CCSD(T) methodology and aug-cc-pwCVQZ AO basis. All values are in atomic units. . . . . . . . . . . . . . . . . . . T3 Polarizability components (α ⊥ and α ∥ ) and invariants (ᾱ and γ) of HF calculated with with CCSD(T) methodology and aug-cc-pwCVQZ AO basis, along with one 5p4d3f bond-function basis. All values are in atomic units. For more details on the exponents of the bond-functions and their location, refer to the Sec.

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“…Despite the difficulty of laboratory measurements, HF and HCl line shapes were recorded for the (1-0) and (2-0) vibrational bands [238][239][240][241] as well as for the pure rotational J = 1←0 transitions [242][243][244] in mixtures with N 2 , O 2 , Ne, Ar and Xe. In Ref.…”

Section: Hf and Hcl Moleculesmentioning

confidence: 99%

Pressure broadening and shifting of vibrotational lines of atmospheric gases

Buldyreva¹,

Lavrentieva²,

Starikov³

2010

Collisional Line Broadening and Shifting of Atmospheric Gases

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Water vapour is one of the strongest absorbers of radiation in the Earth's atmosphere, but some other gases also play an important role in the atmospheric radiative transfer processes: carbon dioxide CO 2 , carbon monoxide CO, ozone О 3 , methane CH 4 . Minor atmospheric pollutants such as hydrogen sulphide H 2 S, methyl fluoride CH 3 F, methyl chloride CH 3 Cl, ethylene C 2 H 4 , nitric oxide NO, nitrous oxide N 2 O and nitrogen dioxide NO 2 are equally recognised for their implication in the fundamental chemical reactions occurring in the terrestrial atmosphere. As a consequence, a lot of spectroscopic studies are made for these molecules in order to obtain the line positions, intensities and widths. They are briefly summarised below, starting by asymmetric waterlike molecules of X 2 Y-type which have the same selection rules for vibrotational spectra. Vibrotational lines of asymmetric X 2 Y moleculesBetween asymmetric tops of the X 2 Y type most attention in the spectroscopic literature is paid to the H 2 S, SO 2 , O 3 and NO 2 molecules. _________________________________________________________________ A vibrotational state (v 1 v 2 v 3 ) [J K a K c ] of these molecules is characterised by three vibrational quantum numbers v 1 , v 2 , v 3 and three rotational quantum numbers J, K a , K c . In the NO 2 molecule, having an unpaired electron (total electronic spin S = 1/2), each vibrotational level is split by the spin-rotational interaction into two components (J = N ± S) denoted by + or -, and the three rotational quantum numbers are N, K a , K c . For a given set of vibrotational quantum numbers the corresponding energies are obtained by a diagonalization of the effective Hamiltonian matrix of Eq. (3.

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Absorption profiles of HCl for the J=1–0 rotational transition: Foreign-gas effects measured for N2, O2, and Ar

Cited by 17 publications

References 31 publications

Narrowing broadening and shifting parameters for R(2) and P(14) lines in the HCl fundamental band perturbed by N2 and rare gases from tunable diode laser spectroscopy

Narrowing broadening and shifting parameters for R(2) and P(14) lines in the HCl fundamental band perturbed by N2 and rare gases from tunable diode laser spectroscopy

Testing the limitations of harmonic approximation in the determination of Raman intensities

Pressure broadening and shifting of vibrotational lines of atmospheric gases

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