Experimental and theoretical study of line mixing in methane spectra.: I.: The N2-broadened ν3 band at room temperature

被引:63
作者
Pieroni, D
Nguyen-Van-Thanh
Brodbeck, C
Claveau, C
Valentin, A
Hartmann, JM [1 ]
Gabard, T
Champion, JP
Bermejo, D
Domenech, JL
机构
[1] Univ Paris Sud, CNRS, UPR 136, Lab Phys Mol & Applicat, F-91405 Orsay, France
[2] Univ Paris 06, CNRS, UPR 136, Lab Phys Mol & Applicat, F-75252 Paris 05, France
[3] Univ Bourgogne, CNRS, Unite Associee, Phys Lab, F-21011 Dijon, France
[4] CSIC, Inst Estructura Mat, E-28006 Madrid, Spain
关键词
D O I
10.1063/1.478724
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Line-mixing effects have been studied in the nu(3) band of CH4 perturbed by N-2 at room temperature. New measurements have been made and a model is proposed which is not, for the first time, strictly empirical. Three different experimental set ups have been used in order to measure absorption in the 2800-3200 cm(-1) spectral region for total pressures in the 0.25-2 and 25-80 atm ranges. Analysis of the spectra demonstrates the significant influence of line mixing on the shape of the Q branch and of the P and R manifolds. A model is proposed which is based on state-to-state collisional transfer rates calculated from the intermolecular potential surface with a semiclassical approach. The line-coupling relaxation matrix is constructed from these data and two additional parameters which are fitted on measured absorption. Comparisons between measurements and spectra computed accounting for and neglecting line mixing are made. They prove the quality of the approach which satisfactory accounts for the effects of pressure and of rotational quantum numbers on the spectral shape under conditions where modifications introduced by line mixing are important. For high rotational quantum number lines, the main features induced by collisions are predicted but some discrepancies remain; the latter may be due to improper line-coupling elements but there is strong evidence that the use of inaccurate line broadening parameters also contributes to errors in calculated spectra. (C) 1999 American Institute of Physics. [S0021-9606(99)00116-6].
引用
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页码:7717 / 7732
页数:16
相关论文
共 51 条
[31]   A NEW DIRECT INFRARED-LASER ABSORPTION METHOD FOR STATE-TO-STATE ROTATIONAL ENERGY-TRANSFER IN CROSSED SUPERSONIC JETS - EXPERIMENTAL RESULTS AND QUANTUM SCATTERING ANALYSIS FOR AR+CH4 [J].
NESBITT, DJ ;
NIBLER, JW ;
SCHIFFMAN, A ;
CHAPMAN, WB ;
HUTSON, JM .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (12) :9513-9522
[32]   A SYMMETRY-BASED MODEL FOR SELECTIVE ROTATIONAL ENERGY-TRANSFER IN COLLISIONS OF SPHERICAL TOP MOLECULES [J].
PARSON, R .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (12) :8731-8738
[33]   EXPERIMENTAL AND THEORETICAL-STUDY OF THE ROVIBRATIONAL RELAXATION OF CH4 AND CD4 BY AR [J].
PERRIN, MY ;
JOLICARD, G .
CHEMICAL PHYSICS, 1984, 91 (03) :341-353
[34]   CLOSE-COUPLING AND COUPLED STATES CALCULATION OF LOW-ENERGY HE-CH4 AND NE-CH4 COLLISIONS [J].
PHILLIPS, T ;
SECREST, D .
JOURNAL OF CHEMICAL PHYSICS, 1989, 91 (05) :2840-2847
[35]   Line mixing sum rules for the analysis of multiplet spectra [J].
Pine, AS .
JOURNAL OF QUANTITATIVE SPECTROSCOPY & RADIATIVE TRANSFER, 1997, 57 (02) :145-155
[36]   N-2 and Ar broadening and line mixing in the P and R branches of the nu(3) band of CH4 [J].
Pine, AS .
JOURNAL OF QUANTITATIVE SPECTROSCOPY & RADIATIVE TRANSFER, 1997, 57 (02) :157-176
[38]   Q-branch line mixing effects in the (20(0)0)(I)<-01(1)0 and (12(2)0)(I)<-01(1)0 bands of carbon dioxide perturbed by N-2, O-2, and Ar and in the 13(1)0<-00(0)0 and 13(1)0<-01(1)0 bands of pure nitrous oxide [J].
Rachet, F ;
MargottinMaclou, M ;
Henry, A ;
Valentin, A .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1996, 175 (02) :315-326
[39]   Temperature, pressure, and perturber dependencies of line-mixing effects in CO2 infrared spectra.: II.: Rotational angular momentum relaxation and spectral shift in Σ←Σ bands [J].
Rodrigues, R ;
Boulet, C ;
Bonamy, L ;
Hartmann, JM .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (08) :3037-3047
[40]   Temperature, pressure, and perturber dependencies of line-mixing effects in CO2 infrared spectra .1. Sigma<-Pi branches [J].
Rodrigues, R ;
Khalil, B ;
LeDoucen, R ;
Bonamy, L ;
Hartmann, JM .
JOURNAL OF CHEMICAL PHYSICS, 1997, 107 (11) :4118-4132