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Loewenstein, M.

Publications and source records attributed to Loewenstein, M..

102 records · Page 6

Measurement of NO and O3 from aircraft: 1977 tropical convergence zone experiment

As part of the Ames Research Center program to explore the nature of stratosphere-troposphere exchange processes occurring in the Intertropical Convergence Zone, simultaneous in situ measurements of nitric oxide and ozone mixing ratios were made with the Ames stratospheric air sampler SAS 2. The SAS 2 is a second-generation system; it employs four parallel sensors and was designed primarily for measurements at altitudes of 60,000 ft and above on the U-2 stratospheric research aircraft. The only modifications required for this study was the addition of an air sample flow restrictor. Data were obtained with the SAS 2 system on July 26, 27, 30 and 31, 1977. Generally, 30-min measurements were made at each of six altitudes ranging from 45,000 ft to 70,000 ft, and separated by 5,000 ft intervals.

Starr, W. L.

Stratospheric NO and HNO3 observations in the Northern Hemisphere for three seasons

NO, HNO3, and O3 levels and air temperature were measured as a function of latitude in the 18 to 21 km region of the stratosphere, and the sum of odd nitrogen, equal to NO + NO2 + HNO3, was calculated and compared with model predictions. (NO2 values were inferred from photochemical equilibrium characteristics.) The data show that NO measurements generally exhibit good agreement with model predictions for low and midlatitudes but poor agreement at high latitudes. The experimental sum of odd nitrogen mixing ratios and model predictions agree within a factor of 2-1/2 or better at both 20 and 40 deg N, and show excellent agreement for latitudinal dependence.

Loewenstein, M.

Geographical variations of NO and O3 in the lower stratosphere

Nitric oxide and ozone concentrations in the lower stratosphere have been measured from a high-altitude research aircraft using in situ measuring techniques. Results of several geographical surveys are presented along with predictions of two two-dimensional stratospheric models. Meridional and zonal data were obtained in June 1974 and in June, July, and August 1975. At longitudes 122-158 deg W the meridional data taken between 5 and 80 deg N latitude show an increasing NO concentration with latitude, by a factor of 4 at 21-km altitude and a less marked increase at 18 km. The minimum NO concentration at 21 km is observed at 5 deg N latitude and is about 6 x 10 to the 8th power/cu cm. Zonal data at latitudes 22-38 deg N taken from 55 to 176 deg N longitude show little variation of the NO and O3 concentrations with longitude.

Loewenstein, M.

Seasonal variations of NO and O3 at altitudes of 18.3 and 21.3 km

Nitric oxide and ozone concentrations have been measured in situ from a high-altitude research aircraft. Data which show the variations of NO and O3 with the time of year are presented for altitudes of 18.3 and 21.3 km. The extreme values of the observed NO concentrations at 21.3 km are 1.2 billion per cu cm in summer and 0.2 billion per cu cm in winter. At 18.3 km the extreme values are 1.6 billion per cu cm in summer and 0.1 billion per cu cm in winter. The smoothed NO seasonal data show a variation of about a factor of 2.5 at 21.3 km and a factor of 4 at 18.3 km. The ozone data show the generally expected magnitude and seasonal variation. We have used a photochemical model employing the measured ozone concentrations, the mean solar zenith angle, and seasonal HNO3 data reported by others to predict the seasonal NO variation at 20 km. The result is a summer-to-winter NO ratio of 2.5 which is in fair agreement with the observed ratios.

Loewenstein, M.

NO and O3 measurements in the lower stratosphere from a U-2 aircraft

In situ measurements of nitric oxide and ozone were carried out at altitudes up to 21 km during two flights of a U-2 aircraft on Dec. 6 and 18, 1973, over the west coast of the United States. A chemiluminescent detector based on the luminescent reaction of nitric acid with excess ozone was used in nitric acid measurements. Ozone concentration measurements were based on the absorption of the Hg line at 2,537 A in the Hartley continuum. The results are compared with available data.

Loewenstein, M.

Measurements of supersonic jet aircraft wakes in the stratosphere

Progress is reported in an experimental program consisting of making supersonic aircraft wakes visible in the stratosphere so that photographs can be taken which yield wake dimensions vs time, and so that aircraft equipped with instruments which measure key exhaust species can find and penetrate the wakes. The object is to provide verification of fluid dynamic and chemical models. Three available models are summarized, and the experimental methods used are described. The Lockheed model predictions correspond in general most closely to experimental wake cross-sectional aerea. NO data are in reasonable agreement with NO predictions, but chemical models are relatively undeveloped, and additional measurements of exhaust products are needed before verification of chemical models becomes possible. However, the overall feasibility of wake visualization for model verification is substantiated. It is emphasized that significant model differences exist that must be resolved before reliable predictions can be made in the wake regimes studied.

Farlow, N. H.

Instrumentation for air quality measurements.

Comparison of the new generation of air quality monitoring instruments with some more traditional methods. The first generation of air quality measurement instruments, based on the use of oxidant coulometric cells, nitrogen oxide colorimetry, carbon monoxide infrared analyzers, and other types of detectors, is compared with new techniques now coming into wide use in the air monitoring field and involving the use of chemiluminescent reactions, optical absorption detectors, a refinement of the carbon monoxide infrared analyzer, electrochemical cells based on solid electrolytes, and laser detectors.

Loewenstein, M.

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.