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Woods, D. C.

Publications and source records attributed to Woods, D. C..

At least 19 records
All sourcesNASA NTRSDOE OSTI
NASA NTRS1993

In situ observations of aerosol and chlorine monoxide after the 1991 eruption of Mount Pinatubo - Effect of reactions on sulfate aerosol

Highly resolved aerosol size distributions measured from high-altitude aircraft can be used to describe the effect of the 1991 eruption of Mount Pinatubo on the stratospheric aerosol. In some air masses, aerosol mass mixing ratios increased by factors exceeding 100 and aerosol surface area concentrations increased by factors of 30 or more. Increases in aerosol surface area concentration were accompanied by increases in chlorine monoxide at mid-latitudes when confounding factors were controlled. This observation supports the assertion that reactions occurring on the aerosol can increase the fraction of stratospheric chlorine that occurs in ozone-destroying forms.

Wilson, J. C.↗
NASA NTRS1992

Lidar Observations of the Pinatubo Volcanic Cloud over Hampton, Virginia

A series of eruptions of Mt. Pinatubo climaxed in a cataclysmic eruption on June 15-16, which greatly perturbed the stratospheric aerosol layer. These eruptions yielded an estimated 20 megatons of SO2, which is three times the amount produced by El Chichon. Lidar measurements taken by the 48-inch lidar system at Langley Research Center show the vertical distribution, intensity and spread of the Pinatubo aerosol layers over the middle latitude locations. A few observations have also been made using an airborne lidar system which measures scattering and depolarization. The magnitude and transport time of the volcanic aerosols following Pinatubo and El Chichon are compared. In addition, comparisons are made between the ground-based lidar measurements and near-coincident Stratospheric Aerosol and Gas Experiment (SAGE) 2 satellite observations of the Pinatubo aerosol layers.

Osborn, M. T.↗
NASA NTRS1985

Halite particles injected into the stratosphere by the 1982 El Chichon eruption

A cascade impactor was flown on board a U-2 aircraft to gather particulate samples in the stratosphere at 18-21 km altitude after the El Chichon eruptions of 1982. Halite particles were observed, which posed a hazard for the catalytic destruction of ozone. No halite particles were observed a month after the eruptions, while a 40 percent increase in HCl was detected at 12 km, an increase which could have been augmented by halite transformations. The halite proportion of the volcanic clouds was of the same proportion of NaCl as in the volcanic ash around El Chichon. The results indicate that halite forms in eruption clouds of volcanos with alkalic magmas.

Woods, D. C.↗
NASA NTRS1984

Sulfur dioxide and particles in quiescent volcanic plumes from Poas, Arenal, and Colima volcanos, Costa Rica and Mexico

Measurements of SO2 emission rates and concentrations and of particle distribution, size, shape, and composition were made in quiescent volcanic plumes emitted into the troposphere from Poas and Arenal volcanos, Costa Rica, and Colima volcano, Mexico. SO2 emission rates were 700 + or - 180 metric tons per day (t/d) for Poas, 210 + or - 30 t/d for Arenal, and 320 + or - 50 t/d for Colima. The concentrations of SO2 calculated from the COSPEC/lidar data were 5-380 ppb. Concentrations of SO2 measured directly by flame photometry were 10-250 ppb. Particles collected in the plumes with a quartz crystal microbalance impactor were mostly less than 3 microns in diameter and consisted of droplets of dilute sulfur-bearing solutions and minor amounts of layer silicate particles coated with a sulfur-bearing film or crust. Total particle concentrations were 4.7 micrograms per cu.m for Poas and 18.8 micrograms per cu.m for Colima. Comparison of concentrations of SO2 in the plumes with gas samples collected at fumaroles on the ground suggests that the plumes are diluted by the atmosphere by factors of up to 100,000.

Casadevall, T. J.↗
NASA NTRS1984

The appearance of carbon aerosol particles in the lower stratosphere

Very small carbonaceous particles, thought to be meteoritic, have been found in small quantities in the lower stratosphere during aircraft sampling flights. The sampling was accomplished using a quartz crystal microbalance (QCM) cascade impactor operating on a U-2 aircraft as it flew stratospheric sampling missions. Post flight analyses of the samples using scanning electron microscopy, X-ray energy spectroscopy and Auger electron spectroscopy have identified carbon particles 0.1 micron aerodynamic diameter and smaller in 16 of 28 sets of samples obtained between 1979 and 1983. The presence of such carbon particles in the stratosphere has implications relating to global climate, to the conversion of SO2 to sulfuric acid, and to the phenomenon of the Arctic haze.

Chuan, R. L.↗
NASA NTRS1984

Airborne measurements of launch vehicle effluent of STS-2 launch on November 12, 1981 at Cape Canaveral, Florida

The second Space Shuttle (STS-2) was launched from the John F. Kennedy Space Center at 1010 EST on November 12, 1981. An instrumented light airplane was used to measure the emitted concentration of Shuttle exhaust products produced during launch. The airplane accomplished 31 passes through and under the exhaust cloud in the 1 hr 45 min immediately following the launch. Measurements included the following: (1) particulate data in the form of a light scattering coefficient obtained from an integrating nephelometer, (2) particulate concentrations and mass concentrations obtained from a spectrometer probe, (3) gaseous HCl and total HCl concentrations obtained from a gas-filter-correlation instrument and a chemiluminescent instrument, respectively, and (4) outside-air temperature and dew-point temperature. These data are presented along with time, altitude, and position for each cloud pass. These data are within the range of values observed during similar measurements made during the first Space Shuttle launch on April 12, 1981.

Maddrea, G. L., Jr.↗
NASA NTRS1984

Hydrogen chloride and aerosol ground cloud characteristics resulting from Space Shuttle launches

Airborne measurements of gaseous HCl, gaseous and aerosol HCl, particulates, relative humidity and temperature were obtained in ground clouds produced during three Space Shuttle launches. Partitioning of HCl between HCl aerosol and gaseous HCl was investigated as the solid rocket exhaust cloud diluted with ambient air to evaluate the conditions under which aerosol formation occurs in the troposphere in the presence of hygroscopic HCl vapor. Equilibrium predictions for aqueous HCl aerosol formation generally agree with the measured HCl partitioning over HCl concentrations from 0.5 to 36 ppm. HCl concentration dispersion within four cloud segments at time t (min) was evaluated using the expression C = C(0) (t to the alpha power) where C(0) varied from 145 to 2250 ppm and alpha varied from -1.14 to -1.73. Aerosol fallout from the exhaust clouds was measured with time by monitoring HCl concentrations and aerosol distributions 100 m below the cloud as it drifted away from the launch site. Significant amounts of HCl were found to be removed by fallout of particles in the 80-220 micron diameter range up to 30 min after launch.

Sebacher, D. I.↗
NASA NTRS1983

Size-specific composition of aerosols in the El Chichon volcanic cloud

A NASA U-2 research aircraft flew sampling missions in April, May, July, November, and December 1982 aimed at obtaining in situ data in the stratospheric cloud produced from the March-April 1982 El Chichon eruptions. Post flight analyses provided information on the aerosol composition and morphology. The particles ranged in size from smaller than 0.05 m to larger than 20 m diameter and were quite complex in composition. In the April, May, and July samples the aerosol mass was dominated by magmatic and lithic particles larger than about 3 m. The submicron particles consisted largely of sulfuric acid. Halite particles, believed to be related to a salt dome beneath El Chichon, were collected in the stratosphere in April and May. On the July 23 flight, copper-zinc oxide particles were collected. In July, November, and December, in addition to the volcanic ash and acid particles, carbon-rich particles smaller than about 0.1 m aerodynamic diameter were abundant.

Woods, D. C.↗
NASA NTRS1983

Airborne measurements of launch vehicle effluent: Launch of Space Shuttle (STS-1) on 12 April 1981

Launch vehicle effluent environmental impact activities from the first space shuttle (STS-1) included airborne measurements within the exhaust cloud from about 9 min after launch (T + 9) to T + 120 min. Measurements included total hydrogen chloride (gaseous plus aqueous) concentrations, particulate concentrations, temperature, and dewpoint temperature. The airborne measurements are summarized. The physical growth and behavior of exhaust clouds is presented as well as the results of laboratory analysis of elemental composition of particulate samples collected by the aircraft. Observed results from the STS-1 launch are compared with earlier Titan III results. Shuttle effluent concentrations are found to be within the range of Titan III observations.

Gregory, G. L.↗
NASA NTRS1982

Research on atmospheric volcanic emissions - An overview

Atmospheric abundances and the geochemical cycle of certain volatile compounds and elements may be largely influenced or entirely controlled by magmatic sources. However, better estimates of the magnitude and variability of volcanic emissions are required if the importance of this natural source of atmospheric constituents and the resulting effect on atmospheric chemistry are to be elucidated. The project 'Research on Atmospheric Volcanic Emissions' (RAVE) is concerned with the improvement of knowledge of both geological and chemical phenomena attending these emissions by means of comprehensive instrumentation on board a research aircraft making simultaneous measurements of plume constituents. A description is presented of the equipment and the procedures used in the RAVE field study of Mt. St. Helens' plume. An overview of the results is also provided.

Friend, J. P.↗
NASA NTRS1982

Small particles in plumes of Mount St. Helens

Particles in the size range 0.1-25 microns were sampled by aircraft carrying a quartz crystal microcascade in the Mount St. Helens plume on three dates in August and September 1980. Two of the sampling dates represented 'typical' emissions of the volcano between plinian eruptions. One sampling flight was made 1-4 hours before the small plinian eruption of August 7, 1980 when the plume had become discontinuous and visibly darker. The plume sampled on August 7, before the eruption, contained mainly approximately 2-micron diameter silicic glass particles, fragments of the Mount St. Helens magma. The typical plumes sampled on September 22 and August 6 had much smaller concentrations of particles, trimodal size distributions with peaks at 10, 0.4, and 0.1 microns. The particles were largely nonsilicate and apparently represented Cu-Zn oxide (10 micron peak), Al sulfate, chloride, and oxide, and sulfuric acid (smallest size peak).

Rose, W. I.↗
NASA NTRS1982

Fine particles in the Soufriere eruption plume

The size distributions of fine particles measured at tropospheric altitudes in the periphery of the eruption plume formed during the April 17, 1979 eruption of Soufriere Volcano and in the low-level effluents on May 15, 1979 were found to be bimodal, having peak concentrations at geometric mean diameters of 1.1 and 0.23 micrometers. Scanning electron microscopy and energy-dispersive X-ray analysis of the samples revealed an abundance of aluminum and silicon and traces of sodium, magnesium, chlorine, potassium, calcium, and iron in the large-particle mode. The submicrometer-sized particles were covered with liquid containing sulfur, assumed to be in the form of liquid sulfuric acid.

Woods, D. C.↗
NASA NTRS1981

Satellite and correlative measurements of the stratospheric aerosol. II Comparison of measurements made by SAM II, dustsondes and airborne lidar

Results are shown from the first set of measurements conducted to validate extinction data from the Stratospheric Aerosol Measurement II (SAM II). Dustsonde-measured number density profiles and lidar-measured backscattering profiles for two days are converted to extinction profiles, and are shown to agree within their respective uncertainties at all heights above the tropopause. Near the tropopause, agreement depends on use of model size distributions with larger particles, having radii greater than 0.6 microns. The presence of such large particles is supported by measurements made elsewhere, is suggested by the in situ size distribution measurements reported, and is likely to have an important bearing on the radiative impact of the total stratospheric aerosol. It is concluded that the SAM II extinction data and uncertainty estimates are supported.

Russell, P. B.↗
NASA NTRS1981

Characterization of aerosols from eruptions of Mount St. Helens

Measurements of mass concentration and size distribution of aerosols from eruptions of Mount St. Helens as well as morphological and elemental analyses were obtained between 7 April and 7 August 1980. In situ measurements were made in early phreatic and later, minor phreatomagmatic eruption clouds near the vent of the volcano and in plumes injected into the stratosphere from the major eruptions of 18 and 25 May. The phreatic aerosol was characterized by an essentially monomodal size distribution dominated by silicate particles larger than 10 micrometers in diameter. The phreatomagmatic eruption cloud was multimodal; the large size mode consisted of silicate particles and the small size modes were made up of mixtures of sulfuric acid and silicate particles. The stratospheric aerosol from the main eruption exhibited a characteristic narrow single mode with particles less than 1 micrometer in diameter and nearly all of the mass made up of sulfuric acid droplets.

Chuan, R. L.↗
NASA NTRS1980

Examples of realistic aerosol particles collected in a cascade impactor

In this paper some scanning electron microscope photomicrographs showing examples of a variety of particulate aerosol shapes are presented. Compositions of particles also are presented. These particles represent samples from a number of different sources and locations including: solid propellant rocket motor plumes, active volcano plumes, the lower stratosphere over Sondrestrom, Greenland, and the upper troposphere over northern Texas. The particles were collected from aboard an aircraft with a cascade impactor which classified them according to aerodynamic size into 10 size intervals ranging from submicron to greater than 25 micrometers in diameter. The cascade impactor also served to measure the mass concentration as a function of particle size. The variety of shapes and compositions found among these particles suggest difficulties in obtaining reliable size distribution data from light scattering measurements.

Woods, D. C.↗
NASA NTRS1979

Launch vehicle effluent measurements during the May 12, 1977, Titan 3 launch at Air Force Eastern Test Range

Airborne effluent measurements and cloud physical behavior for the May 21, 1977, Titan 3 launch from the Air Force Eastern Test Range, Fla. are presented. The monitoring program included airborne effluent measurements in situ in the launch cloud, visible and infrared photography of cloud growth and physical behavior, and limited surface collection of rain samples. Airborne effluent measurements included concentrations of HCl, NO, NOx, and aerosols as a function of time in the exhaust cloud. For the first time in situ particulate mass concentration and aerosol number density were measured as a function of time and size in the size range of 0.05 to 25 micro meters diameter. Measurement results were similar to those of earlier launch monitorings. Maximum HCl and NOx concentrations ranged from 10 ppm and 500 ppb, respectively, several minutes after launch to about 1 ppm and 100 ppb at 45 minutes after launch.

Gregory, G. L.↗
NASA NTRS1979

Launch vehicle effluent measurements during the August 20, 1977, Titan 3 launch at Air Force Eastern Test Range

Airborne effluent measurements within the launch cloud and visible and infrared measurements of cloud physical behavior are discussed. Airborne effluent measurements include concentrations of HCl, Cl2, NO, NOX, and particulates as a function of time during each sampling pass through the exhaust cloud. The particle size distribution was measured for each pass through the cloud. Mass concentration as a function of particle diameter was measured over the size range of 0.05- to 25 micron diameter, and particle number density was measured as a function of diameter over a size range of 0.5 to 7.5 micron. Effluent concentrations in the cloud ranged from about 30 ppm several minutes after launch to about 1 to 2 ppm at 100 minutes. Maximum Cl2 concentrations were about 40 to 55 ppb and by 20 minutes were less than 1.0 ppb. A tabulated listing of the airborne data is given in the appendix. Usable cloud imaging data were limited to the first 16 minutes after launch.

Woods, D. C.↗