Target density dependence of molecule-molecule absolute total scattering cross sections
Creators
- 1. Department of Chemistry and James Franck Institute, The University of Chicago, Chicago, Illinois 60637
Description
The target density dependence of absolute total cross sections for LiF scattered by CO, CO2, CHF3, CH4, D2, and Ar was studied at a LiF velocity of 1.5 × 105 cm/sec and a target temperature of 297°K. The experiments were performed under conditions of high angular resolution in order to observe the full quantum mechanical cross section. For the systems LiF–CO, LiF–CO2, and LiF–CHF3 there was a substantial variation of observed cross section with density, while for LiF–CH4, LiF–D2, and LiF–Ar there was no observable variation. It is shown that the target transmission is the Laplace transform of the cross section distribution function. Information was obtained about the distribution of cross sections as a function of the internal state of LiF by fitting model distributions to the data. For the lower LiF rotational states the LiF–CO and LiF–CO3 cross sections are dominated by the dipole-quadrupole interaction and are determined at the outermost impact parameters by processes inelastic in the rotation of LiF, and inelastic and/or elastic in the targets CO of CO2; for the higher LiF rotational states the total cross section is determined mainly by elastic processes and is therefore dominated by induction and dispersion interactions. The dipole-quadrupole scattering effect, so important in microwave line broadening theories, thus has been identified in experiments of this type. For LiF–CHF3 the largest total cross sections are determined by dipole-dipole inelastic scattering. For those targets which showed no pressure dependence (Ar, D2, and CH4) the standard deviation of the cross sections was less than ∼15 percent of the mean as determined by the accuracy of the experiments and the range of target densities used. This is consistent with the symmetry of the interaction and the possible degree of anistropy. No rotational inelasticity could be inferred for these targets. A theoretical analysis of the distribution of cross sections based on dipole-quadrupole and dipole-dipole scattering processes is presented. Various fitted models for the distribution of cross sections can be evaluated in the light of these analyses.
Additional details
Additional titles
- Augmented title (English)
- LiF collisions with CO, CO_2, CHF_3, CH_4, D_2, and Ar, thermal energies
Identifiers
- DOI
- 10.1063/1.1681719;
Publishing Information
- Journal Title
- The Journal of Chemical Physics
- Journal Volume
- 61
- Journal Issue
- 10
- Series
- J. Chem. Phys.
- Journal Page Range
- 4209-4216
- ISSN
- 0021-9606
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 6173863
- Subject category
- S74: ATOMIC AND MOLECULAR PHYSICS;
- Descriptors DEI
- ARGON; ATOM-MOLECULE COLLISIONS; CARBON DIOXIDE; CARBON MONOXIDE; DEUTERIUM; FLUOROFORM; INTERMOLECULAR FORCES; LITHIUM FLUORIDES; MEDIUM TEMPERATURE; METHANE; MOLECULE-MOLECULE COLLISIONS; ROTATIONAL STATES; TOTAL CROSS SECTIONS
- Descriptors DEC
- ALKALI METAL COMPOUNDS; ALKANES; ATOM COLLISIONS; CARBON COMPOUNDS; CARBON OXIDES; CHALCOGENIDES; COLLISIONS; CROSS SECTIONS; ELEMENTS; ENERGY LEVELS; EXCITED STATES; FLUORIDES; FLUORINE COMPOUNDS; HALIDES; HALOGEN COMPOUNDS; HYDROCARBONS; HYDROGEN ISOTOPES; ISOTOPES; LIGHT NUCLEI; LITHIUM COMPOUNDS; MOLECULE COLLISIONS; NONMETALS; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANIC FLUORINE COMPOUNDS; ORGANIC HALOGEN COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; RARE GASES; STABLE ISOTOPES
Optional Information
- Notes
- Updated automatically by Metadata and Full-Text Enrichment Agent