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At least 91 records · Page 5
All sourcesNASA NTRSDOE OSTI
NASA NTRS1988

Midlatitude ClO below 22 km altitude - Measurements with a new aircraft-borne instrument

Midlatitude stratospheric ClO at altitudes below 22 km has been measured for the first time. Measurements were made at latitudes between 27 and 48 deg N during three flights from Moffett Field, CA, in June and July of 1987, with a new instrument flown on the NASA ER-2 aircraft. The result from these flights is that the ClO mixing ratio increases from less than 0.5 pptv at 16.8 km to 2.0 pptv at 18.3 km and 10.1 pptv at 21 km. These altitude profiles agree with an extrapolated profile from a May 1986 balloon-borne experiment (Brune and Anderson, 1986).

Brune, Wm. H.↗
NASA NTRS1988

Formation of the Antarctic ozone hole by the ClO dimer mechanism

New measurements of the low-altitude ClO profile, made during September 1987, are presented along with detailed observations of ozone depletion over McMurdo Station, Antarctica during the same period. The results show that both the rate and altitude range of ozone depletion can be quantitatively accounted for by a mechanism in which the ClO dimer is the important intermediary in the catalytic destruction of ozone. An alternative bromine mechanism appears capable of contributing only 5-15 percent to the ozone loss rate.

Barrett, J. W.↗
NASA NTRS1989

Infrared line intensity measurements in the v = 0-1 band of the ClO radical

Integrated line intensity measurements in the ClO-radical fundamental vibrational v = 0-1 band were carried out using a high-resolution Fourier transform spectrometer coupled to a long-path-length absorption cell. The results of a series of measurements designed to minimize systematic errors, yielded a value of the fundamental IR band intensity of the ClO-radical equal to 9.68 + or - 1.45/sq cm per atm at 296 K. This result is consistent with all the earlier published results, with the exception of measurements reported by Kostiuk et al. (1986) and Lang et al. (1988).

Burkholder, James B.↗
NASA NTRS1989

Ozone destruction by chlorine radicals within the Antarctic vortex - The spatial and temporal evolution of ClO-O3 anticorrelation based on in situ ER-2 data

The chemical evolution of the Antarctic vortex region was studied during August 23-September 22, 1987 on the basis of in situ O3 and ClO data collected by the ER-2 aircraft. Particular attention is given to the evolution of the ClO-O3 anticorrelation from the first flight on August 23, 1987, which penetrated well into the vortex, through the course of 10 flights culminating on September 22, 1987. It is concluded that the disappearance of ozone within the Antarctic vortex results from halogen-catalyzed recombination of O3 to molecular oxygen.

Anderson, J. G.↗
NASA NTRS1989

Kinetics and product studies of the reaction ClO + BrO using discharge-flow mass spectrometry

The kinetics and product branching ratios of the reaction between ClO and BrO were studied at 1 torr pressure over the temperature range 220-400 K, using the method of discharge-flow mass spectrometry. Three product channels were identified and quantified: Br + ClOO, Br + OClO, and BrCl + O2, indicating that the reaction mechanism of ClO + BrO involves metastable intermediates. The overall reaction rate coefficient and the rate coefficients for the three channel reactions are given.

Friedl, Randall R.↗
NASA NTRS1990

In situ observations of ClO in the Arctic Stratosphere - ER-2 aircraft results from 59 deg N to 80 deg N latitude

Large abundances of ClO were observed inside the Arctic polar vortex during 14 flights of the NASA ER-2 aircraft from Stavanger, Norway (59 deg N, 6 deg E) to 80 deg N latitude. Flights were conducted at altitudes between 14 and 20 km when the solar zenith angle was between 79 and 101 deg. Data are reported for three flights that represent the main features observed during the mission. These data, comparable to those obtained in the Antarctic ozone hole, indicate that the springtime Arctic polar vortex was extensively perturbed by heterogeneous chemistry and contained enough ClO to catalytically destroy ozone rapidly.

Brune, W. H.↗
NASA NTRS1990

The sunrise and sunset variation of ClO in the lower stratosphere

The abundances of ClO have been measured, in situ, in the lower stratosphere during sunrise and sunset. Measurements were made with an instrument mounted on the NASA ER-2 aircraft, which was flown at an altitude of 20 km and latitudes between 35 and 47 deg N during a morning and an evening flight. The abundances of ClO were observed over a dynamic range of 20 from a detection threshold of 1 part per trillion volume (pptv). These data confirm the sunrise variation of the photolysis of chlorine nitrate that is predicted by a zero-dimensional photochemical model. They also suggest that the absolute photolysis and termolecular formation of chlorine nitrate occur at rates consistent with nominal ClONO2 and NO2 concentrations.

Brune, W. H.↗
NASA NTRS1991

Measurements of ClO and O3 from 21 deg N to 61 deg N in the lower stratosphere during February 1988 - Implications for heterogeneous chemistry

The decline in stratospheric ozone at northern midlatitudes in wintertime may be caused by chlorine photochemistry that has been enhanced by heterogeneous reactions. The possibility that the heterogeneous reaction of N2O5 on sulfate aerosols is the cause of this decadal ozone decline is examined by comparing ClO and O3 measurements made in the lower stratosphere during February, 1988, with results from a 2D model. At midlatitudes, the abundances, latitudinal, and seasonal gradients of the observed ClO are similar to the results of a model with heterogeneous chemistry, but are in strong disagreement with the results from the model with only gas-phase chemistry. At low latitudes, agreement is best with the results of the model with only gas-phase chemistry. Limited observations indicate that the amount of reactive chlorine is being enhanced, and that heterogeneous chemistry is a likely cause.

King, J. C.↗
NASA NTRS1993

In situ measurements of ClO at mid-latitudes: Is there an effect from Mt. Pinatubo?

Observations of ClO from 20 to 60 deg N made before and after the eruption of Mt. Pinatubo are compared for changes which may result from increased sulfate aerosol surface area. Using ozone as a vertical coordinate and examining data at similar latitudes and seasons, elevated abundances of ClO are found at low latitudes (20 to 30 deg N), an effect which decreases with increasing latitude. For the flights compared, there appear to be no differences, within the uncertainty of the measurements, at latitudes poleward of 40 deg N. These results are consistent with the idea that the hydrolysis of N2O5 on sulfate aerosols becomes saturated at moderate aerosol loadings.

Avallone, L. M.↗
NASA NTRS1993

Balloon-borne measurements of ClO, NO, and O3 in a volcanic cloud: An analysis of heterogeneous chemistry between 20 and 30 km

Balloon profiles of chlorine monoxide (ClO), nitric oxide (NO), and ozone (O3) were measured on March 11, 1992 from 100 to 10 mb over Greenland (67.0 deg N, 50.6 deg W). Measurements from SAGE II indicate that the aerosol surface area in the region was enhanced by sulfur from the eruption of Mt. Pinatubo, reaching 50 times background near 20 km. Concentrations of ClO were enhanced and concentrations of NO were suppressed relative to low aerosol conditions consistent with the effects of hydrolysis of N2O5 on the surface of sulfuric acid aerosols. The data are consistent with a value of 2 x 10(exp -4) for the reaction probability of the heterogeneous hydrolysis of ClONO2, indicating a minor role for this reaction at as temperature of 220 K. At these temperatures, we find no evidence for the catastrophic loss of ozone predicted to occur under conditions of enhanced aerosol surface area.

Dessler, A. E.↗
NASA NTRS1994

Pressure broadening of ClO by N2 and O2 near 204 and 649 GHz and new frequency measurements between 632 and 725 GHz

The N2 and O2 pressure broadening of the ClO transitions near 204 and 649 GHz have been measured between 200 and 300 K. Oxygen broadening has been measured for the transitions near 278 GHz. The accuracy of the derived air broadening is comparable to that for the air broadening of stable species and is estimated to be within approximately 3% over the entire temperature range. These transitions are currently being used for satellite, balloon, and ground based monitoring of atmospheric ClO, respectively. Some new frequency measurements are reported in the 632 - 725 GHz range. These are in good agreement with previous measurements and predictions.

Oh, J. J.↗
NASA NTRS1996

Stratospheric Chlorine partitioning: Constraints from Shuttle-borne Measurements of [HCl], [ClNO3] and [ClO]

Measured stratospheric mixing ratios of HCl, ClNO3, and ClO from ATMOS and MAS are poorly reproduced by models using recommended kinetic parameters. This discrepancy is not resolved by new rates for the reactions Cl+CH4 and OH+HCl derived from weighted fits to laboratory measurements. A deficit in modeled [HCl] and corresponding overprediction of [ClNO3] and [ClO], which increases with altitude, suggests that production of HCl between 20 and 50 km is much faster than predicted from recommended rates.

Michelsen, H. A.↗
NASA NTRS1993

In Situ Measurements of CLO at Mid-Latitudes: Is there an Effect from Mt. Pinatubo?

Observations of ClO from 20 to 60 deg N made before and after the eruption of Mt. Pinatubo are compared for changes which may result from increased sulfate aerosol surface area. Using ozone as a vertical coordinate and examining data at similar latitudes and seasons, elevated abundances of ClO are found at low latitudes (20 to 30 deg N), an effect which decreases with increasing latitude. For the flights compared, there appear to be no differences, within the uncertainty of the measurements, at latitudes poleward of 40 deg N. These results are consistent with the idea that the hydrolysis of N2O5 on sulfate aerosols becomes saturated at moderate aerosol loadings.

Avallone, L. M.↗
NASA NTRS1993

Balloon-Borne Measurements of CLO, NO and O3 in a Volcanic Cloud: An Analysis of Heterogeneous Chemistry between 20 and 30 KM

Balloon profiles of chlorine monoxide (ClO), nitric oxide (NO), and ozone (O3) were measured on March 11, 1992 from 100 to 10 mb over Greenland (67.0 deg N, 50.6 deg W). Measurements from SAGE II indicate that the aerosol surface area in the region was enhanced by sulfur from the eruption of Mt. Pinatubo, reaching 50 times background near 20 km. Concentrations of ClO were enhanced and concentrations of NO were suppressed relative to low aerosol conditions consistent with the effects of hydrolysis of N2O5 on the surface of sulfuric acid aerosols. The data are consistent with a value of 2 x 10(exp -4) for the reaction probability of the heterogeneous hydrolysis of ClONO2, indicating a minor role for this reaction at a temperature of 220 K. At these temperatures, we find no evidence for the catastrophic loss of ozone predicted to occur under conditions of enhanced aerosol surface area.

Dessler, A. E.↗
NASA NTRS1996

Polar Vortex Conditions During The 1995-96 Arctic Winter: MLS ClO and HNO3

Microwave Limb Sounder (MLS) measurements of lower stratospheric ClO and HNO3 during the 1995-96 Arctic winter are presented. The 1995-96 Arctic winter was both colder and more persistently cold than usual, leading to an enhancement in lower stratospheric ClO of greater magnitude, vertical extent, and duration than previously observed in the Arctic. Vortex concentrations of HNO3 in mid-December were large due to diabatic descent. Trajectory calculations indicate that localized severe depletions of gas-phase HNO3 in mid-February and early March did not arise from entrainment of midlatitude air into the vortex and were therefore probably related to polar stratospheric cloud (PSC) formation. A strong correlation between temperature and gas-phase HNO3 was evident, consistent with recurring PSC condensation and evaporation cycles.

Santee, M. L.↗
DOE OSTI2020

Materials Data on ClO by Materials Project

ClO is Tetraauricupride structured and crystallizes in the cubic Pm-3m space group. The structure is zero-dimensional and consists of one hydrochloric acid molecule and one water molecule.

36 MATERIALS SCIENCE↗
DOE OSTI2020

Materials Data on ClO by Materials Project

ClO is alpha carbon monoxide-like structured and crystallizes in the tetragonal I4_1/amd space group. The structure is zero-dimensional and consists of eight chlorine molecules and eight hydrogen peroxide molecules.

36 MATERIALS SCIENCE↗