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  • 1980-1984  (8)
  • 1
  • 2
    Publication Date: 2006-04-12
    Description: Nineteen stratospheric samples from the eruption plumes of Mount St. Helens were collected in five flight experiments. The plume samples were collected at various altitudes from 13.1 to 20.7 km by using the Ames cryogenic sampling system on board the NASA U-2 aircraft. The enriched, cryogenically collected samples were analyzed by chromatography. The concentrations of aerosols precursor gases (OCS, SO2, and CS2), CH3Cl, N2O, CF2Cl2, and CFCl3 were measured by gas chromatography. Large enhancement of the mixing ratio of SO2 and moderate enhancement of CS2 and OCS were found in the plume samples compared with similar measurement under pre-volcanic conditions. A fast decay rate of the SO2 mixing ratio in the plume was observed. Measurement of Cl(-), SO2(2-), and NO3(-) by ion chromatography was also carried out on water solutions prepared from the plume samples. The results obtained with this technique imply large mixing ratios of HCl, (NO + NO2 + HNO3), and SO2, in which these constituents are the respective sources of the anions. Measurement of the Rn222 concentration in the plume was made. Other stratospheric constituents in the plume samples, such as H2O, CO2, CH4, and CO, were also observed.
    Keywords: GEOPHYSICS
    Type: Atmospheric Effects and Potential Climatic Impact of the 1980 Eruptions of Mt. St. Helens; p 47-54
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  • 3
    Publication Date: 2011-08-18
    Description: Samples of stratospheric trace gases were obtained on eight flights of NASA high-altitude aircraft from April 16 through December 13, 1982. The sampling occurred at altitudes from 15 to 22 km, latitudes from 23 to 52 deg N, and longitudes from 108 to 130 deg W. The cryogenically concentrated samples were analyzed by gas chromatography for SO2, a primary precursor of the gas-to-particle conversion process. The measured mixing ratio of SO2 varied between 8 and 132 pptv. Evidence from aerosol measurements indicates that a few of our early samples may have been collected in the fringes of the volcanic cloud from El Chichon. Samples obtained on some later flights may have been from the eruption cloud but were taken at times when most of the volcanically injected SO2 should have been converted to H2SO4.
    Keywords: GEOPHYSICS
    Type: Geophysical Research Letters (ISSN 0094-8276); 10; 1045-104
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  • 4
    Publication Date: 2011-08-19
    Description: Results from an intercomparison of methods to measure carbon monoxide (CO), nitric oxide (NO), and the hydroxyl radical (OH) are discussed. The intercomparison was conducted at Wallops Island, Virginia, in July 1983 and included a laser differential absorption and three grab sample/gas chromatograph methods for CO, a laser-induced fluorescence (LIF) and two chemiluminescence methods for NO, and two LIF methods and a radiocarbon tracer method for OH. The intercomparison was conducted as a field measurement program involving ambient measurements of CO (150-300 ppbv) and NO (10-180 pptv) from a common manifold with controlled injection of CO in incremental steps from 20 to 500 ppbv and NO in steps from 10 to 220 pptv. Only ambient measurements of OH were made. The agreement between the techniques was on the order of 14 percent for CO and 17 percent for NO. Hardware difficulties during the OH tests resulted in a data base with insufficient data and uncertanties too large to permit a meaningful intercomposition.
    Keywords: GEOPHYSICS
    Type: Journal of Geophysical Research (ISSN 0148-0227); 89; 11819-11
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  • 5
    Publication Date: 2011-08-18
    Description: Measurements in the stratosphere of gaseous constituents in the plume of Mount St. Helens were obtained during five flights of the NASA U-2 aircraft between 19 May and 17 June 1980. Mixing ratios from gas chromatographic measurements on samples acquired about 24 hours after the initial eruption show considerable enhancement over nonvolcanic concentrations for sulfur dioxide (more than 1000 times), methyl chloride (about 10 times), and carbon disulfide (more than 3 times). The mixing ratio of carbonyl sulfide was comparable to nonvolcanic mixing ratios although 3 days later it was enhanced two to three times. Ion chromatography measurements on water-soluble constituents are also reported. Very large concentrations of chloride, nitrate, and sulfate ions were measured, implying large mixing ratios for the water-soluble gaseous constituents from which the anions are derived. Measurements of radon-222 present in the plume are also reported.
    Keywords: GEOPHYSICS
    Type: Science; 211; Feb. 20
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  • 6
    Publication Date: 2019-06-28
    Description: During the 1979 Summer MONEX, 150 air samples collected over Saudi Arabia, India, and the Arabian Sea were analyzed for CO and CH4. Near Dhahran and over the Ganges Valley there were high concentrations of CO, around 300 ppbv, in the boundary layer. Out over the Saudi Arabian desert there was no sharp increase in the boundary layer. It is suggested that these high concentrations originate from pollution sources. Low values of CO, down to 80 ppbv, are found over the Arabian Sea as the monsoon progresses, and these may originate from the Southern Hemisphere. Methane over Saudi Arabia (1.59 ppmv) is a little higher than that over the Arabian Sea (1.54 ppmv) probably because the latter region is influenced by air from the Southern Hemisphere.
    Keywords: METEOROLOGY AND CLIMATOLOGY
    Type: Journal of Geophysical Research; 86; Oct. 20
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  • 7
    Publication Date: 2019-06-28
    Description: Full-scale, in-flight measurements of the boundary-layer thickness, velocity profile, and flow angle have been made at several sample collection stations on the fuselage of the NASA CV 990. These results are given as functions of Mach number, Reynolds number, yaw, and angle of attack.
    Keywords: AERODYNAMICS
    Type: AIAA PAPER 84-0028
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  • 8
    Publication Date: 2019-06-28
    Description: Results of an experimental investigation of the contamination of air sampling inlets by aircraft emissions from the NASA CV-990 research aircraft are presented. This four-engine jet aircraft is a NASA facility used for many different atmospheric and meteorological experiments, as well as for developing spacecraft instrumentation for remote measurements. Our investigations were performed to provide information on which to base the selection of sampling locations for a series of multi-instrument missions for measuring tropospheric trace gases. The major source of contamination is the exhaust from the jet engines, which generate many of the same gases that are of interest in atmospheric chemistry, as well as other gases that may interfere with sampling measurements. The engine exhaust contains these gases in mixing ratios many orders of magnitude greater than those that occur in the clean atmosphere which the missions seek to quantify. Pressurized samples of air were collected simultaneously from a scoop located forward of the engines to represent clean air and from other multiport scoops at various aft positions on the aircraft. The air samples were analyzed in the laboratory by gas chromatography for carbon monoxide, an abundant combustion by-product. Data are presented for various scoop locations under various flight conditions.
    Keywords: AIR TRANSPORTATION AND SAFETY
    Type: AIAA PAPER 84-0029
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