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At least 73 records · Page 4

SO2 absorption cross sections in the near U.V.

In order to understand data measured by the TOMS instrument on Nimbus 7 after the eruption of El Chichon, absorption cross sections are measured in SO2 between 3000 and 3240 A at 295 and 210 K. Errors for these measurements range from less than 2 percent to about 10 percent. Measurements in the 3175 + or 5 A spectral region observed by TOMS indicate that there is a 9 percent reduction in the average cross section at 210 K compared to room-temperature data. Peak cross sections measured at low temperature show increases up to 20 percent over room-temperature data, while cross-section decreases are measured at low temperatures in the areas between the strong features.

Mcgee, Thomas J.↗

Temperature dependence of ozone absorption cross section, 280 to 330 nm

A description is presented of the results of an analysis of the presently available data on the variation of the ozone absorption cross section and the O(1D) yield with temperature. The data used in the analysis of the total ozone cross section were obtained by Inn and Tanaka (1953), Vigroux (1953), and Simons et al. (1973). The O(1D) yield data examined include those of Moortgat et al. (1977), Arnold et al. (1977), and Brock and Watson (1980). For the purposes of the analysis the yield measurements were converted to partial cross sections by multiplying the published yield by the published total cross section.

Hudson, R. D.↗

High resolution absorption cross sections for the A2Pi-X2Pi system of ClO

High-resolution ultraviolet absorption cross-sections for the ClO molecule are obtained, with the aim of facilitating studies of ozone depletion resulting from the injection of chlorofluorocarbons into the atmosphere. The spectroscopic analysis, which involves a frequency-doubled tunable dye laser with a bandwidth of 0.015 A, is described. Studies of the rotational lines of the ClO A 2Pi 3/2-X2Pi 3/2 9-10 band were conducted. Peak cross-sections for the P and R lines of the 9-0 band are found to be 10.0, 9.6, 8.6, 10.6, 10.3, and 9.2 times ten to the negative seventeenth power cm squared, with estimated accuracy of plus or minus 25%. Problems in distinguishing between Cl-35 and Cl-37 absorption are also considered.

Wine, P. H.↗

Sensitivity of N2O, CFCl3, and CF2Cl2 two-dimensional distributions to O2 absorption cross sections

A good test of the transport and ultraviolet radiation treatment for any model can be based on the consideration of the three gases N2O, CFCl3 (F-11), and CF2Cl2 (F-12). Attention is given to a two-dimensional model which makes it possible to study changes in seasonal and latitudinal distributions which result from O2 cross-section changes. A latitude-dependent ozone decrease has already been predicted by two-dimensional models for chlorofluoromethane (CFM) release. For this reason, it is of interest to determine if a strong latitude-dependent change is detectable in the CFM profiles. One-dimensional models have pointed toward a trend of decreased trace gas concentrations in correlation with decreased O2 cross sections. The O2 cross sections between 180 and 230 nm are changed within a range of experimentlly allowed values. It is found that lower O2 absorption cross sections lead to larger photodissociation rates for the trace gases F-11, F-12, and N2O.

Jackman, C. H.↗

Laser measurements of ozone absorption cross sections in the Chappuis band

A sensitive spectrometer has been developed that exploits several He-Ne laser transitions in the visible for precise, high resolution measurements of Chappuis band ozone absorption cross sections at room temperature. An overall uncertainty of better than one percent has been achieved through a combination of transducer calibrations and an experimental technique that unambiguously determines the impurity content of each ozone sample. Results compare favorably with those from most previous analyses in the visible range, though some are obviously lower than this consensus due probably to errors in ozone density measurements.

Anderson, Stuart M.↗

Heavy-ion total and absorption cross sections above 25 MeV/nucleon

Within the context of a double-folding optical potential approximation to the exact nucleus-nucleus multiple-scattering series, eikonal scattering theory is used to generate tables of heavy ion total and absorption cross sections at incident kinetic energies above 25 MeV/nucleon for use in cosmic ray high-energy heavy ion transport and shielding studies. Comparisons of predictions with nucleus-nucleus experimental data show excellent agreement except at the lowest energies, where the eikonal approximation may not be completely valid. Even at the lowest energies, however, agreement is typically within 20 percent.

Townsend, L. W.↗

Radiation and chemistry in the stratosphere - Sensitivity to O2 absorption cross sections in the Herzberg continuum

It is suggested that the discrepancies between observed and modeled vertical profiles of such halocarbons as CFCl3, as well as the problem of simultaneously fitting N2O, CH4, CF2Cl2 and CFCl3 profiles with a single eddy diffusion model, are due to an overestimation of the molecular oxygen absorption cross sections in the 200-220 nm spectral region. The replacement of current O2 cross sections in this range with values that are in better agreement with results for the compounds cited leads to N2O, CF2Cl2 and CFCl3 concentration reductions of factors 0.70, 0.62 and 0.19, respectively. Profiles of CH4, H2 and CO remain unchanged, and the predicted concentration of HNO3 above 30 km is reduced by about 50% for yet another improved fit with observations. It is noted that the correction proposed produces a 30% ozone increase near the 20-25 km peak.

Froidevaux, L.↗

Visible-ultraviolet absorption cross sections for NO2 as a function of temperature

A redetermination of the temperature dependence of the absorption cross-section (sigma) of NO2 in the visible-ultraviolet region was made in order to provide a more reliable data base for the calculation of NO2 photolysis rates in the atmosphere. Experiments over a wide range of temperatures and NO2 concentrations were conducted. The integral of a plot of sigma versus the inverse of the wavelength was essentially independent of temperature. Increasing temperature produced a shift of the spectrum toward longer wavelengths, resulting in a small negative temperature dependence of sigma over the 264-400 nm range and a small positive dependence over the 450-649 nm range. Increasing temperature produced broadening of individual spectral features, resulting in a systematic lowering of peaks and filling of valleys. Recommended cross sections are presented for use in tropospheric NO2 photolysis rate calculations.

Davidson, J. A.↗

Nucleon and heavy-ion total and absorption cross section for selected nuclei

Approximate solutions of the coupled-channel equations for high-energy composite particle scattering are obtained and are applied to the nuclear scattering problem. Relationships between several approximation procedures are established and discussed. The eikonal formalism is used with a small-angle approximation to calculate the coherent elastic scattered amplitude from which total and absorption cross sections are derived. Detailed comparisons with nucleon-nucleus experiments show agreement within 5 percent except at lower energies where the eikonal approximation is of questionable accuracy. Even at these lower energies, agreement is within 15 percent. Tables of cross sections required for cosmic heavy-ion transport and shielding studies are presented.

Wilson, J. W.↗

Experimental upper bounds for resonance-enhanced entangled two-photon absorption cross section of indocyanine green

Resonant intermediate states have been proposed to increase the efficiency of entangled two-photon absorption (ETPA). Although resonance-enhanced ETPA (r-ETPA) has been demonstrated in atomic systems using bright squeezed vacuum, it has not been studied in organic molecules. We investigate for the first time r-ETPA in an organic molecular dye, indocyanine green (ICG), when excited by broadband entangled photons in near-IR. Similar to many reported virtual state mediated ETPA (v-ETPA) measurements, no r-ETPA signals are measured, with an experimental upper bound for the cross section placed at 6(±2) × 10 −23 cm 2 . In addition, the classical resonance-enhanced two-photon absorption (r-TPA) cross section of ICG at 800 nm is measured for the first time to be 20(±13) GM, where 1 GM equals 10 −50 cm 4 s, suggesting that having a resonant intermediate state does not significantly enhance two-photon processes in ICG. Furthermore, the spectrotemporally resolved emission signatures of ICG excited by entangled photons are also presented to support this conclusion.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

High-resolution absorption cross sections of carbon monoxide bands at 295 K between 91.7 and 100.4 nanometers

Theoretical descriptions of the abundance and excitation of carbon monoxide in interstellar clouds require accurate data on the vacuum-ultraviolet absorption spectrum of the molecule. The 6.65 m spectrometer at the Photon Factory synchrotron light source was used to measure photoabsorption cross sections of CO features between 91.2 and 100.4 nm. These data were recorded at a resolving power of 170,000, more than 20 times greater than that used in previous work.

Stark, G.↗

An upper limit for the absorption cross section of the oxygen C 3 Delta u - a 1 Delta g transition

Frederick and Cicerone (1985) have proposed that photodissociation of O2 (a 1 Delta g) by the process O2 (a 1 Delta g) + h-nu + O2 (C 3 Delta u) to O(3 P) + O(3 P) may be a major source of odd oxygen in the upper stratosphere and mesosphere. They argued that, since the process is forbidden only by change in the spin multiplicity, it might have been a cross section intermediate between a fully allowed and a strictly forbidden transition, i.e., 10 to the -20th to 10 to the -19th sq cm near 250 nm. In order to test this proposal, absorption by O2 (a 1 Delta g) has been measured in the 190-290 nm wavelength region. No absorption above the detection limit could be observed for O2 (a 1 Delta g) concentrations of (4-7) x 10 to the 15th/cu cm. An upper limit of 8 x 10 to the -22 sq cm was calculated for the cross section.

Simonaitis, R.↗

Total absorption cross sections of several gases of aeronomic interest at 584 A.

Total photoabsorption cross sections have been measured at 584.3 A for N2, O2, Ar, CO2, CO, NO, N2O, NH3, CH4, H2, and H2S. A monochromator was used to isolate the He I 584 line produced in a helium resonance lamp, and thin aluminum filters were used as absorption cell windows, thereby eliminating possible errors associated with the use of undispersed radiation or windowless cells. Sources of error are examined, and limits of uncertainty are given. Previous relevant cross-sectional measurements and possible error sources are reviewed. Wall adsorption as a source of error in cross-sectional measurements has not previously been considered and is discussed briefly.

Starr, W. L.↗