572 research outputs found

    NASA Dust Mitigation Strategy

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    Chemical characterization of ambient aerosol collected during the northeast monsoon season over the Arabian Sea: Labile-Fe(II) and other trace metals

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    Ambient aerosol samples were collected over the Arabian Sea during the month of March of 1997, aboard the German R/V Sonne, as part of the German Joint Global Ocean Flux Study (JGOFS) project. This is the third study in a series of analogous measurements taken over the Arabian Sea during different seasons of the monsoon. Dichotomous high‐volume collector samples were analyzed for ferrous iron immediately after collection, while trace metals, anions, and cations were determined upon return to the laboratory. The main crustal component was geochemically well represented by the average crustal composition and amounted to 5.94 ± 3.08 μg m−3. An additional crustal constituent of clay‐like character, rich in water‐soluble Ca and Mg, was seen in the fine fraction in air masses of Arabian origin. Total ferrous iron concentrations varied from 3.9 to 17.2 ng m−3 and averaged 9.8 ± 3.4 ng m−3, with 87.2% of Fe(II) present in the fine aerosol fraction. Fe(II) concentrations accounted for on average 1.3 ± 0.5% of the total Fe. While ferrous iron in the coarse fraction appeared to be correlated with the main crustal component, the fine Fe(II) fraction exhibited a more complex behavior. The anthropogenic contribution to the aerosol, as traced by Pb, Zn, and some anions and cations, was found to be considerably larger, especially during the first 10 days of this cruise, than in previously collected samples from the inter‐monsoon and southwest monsoon of 1995

    Development of the Electrostatic Precipitator (ESP) for Mars and Electrodynamic Dust Shield (EDS)

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    Kennedy Space Center's Swamp Works is a fast-paced and diverse technology development laboratory that aims to advance commercial and government capabilities to colonize extraterrestrial environments. As a part of Swamp Works, the Electrostatic and Surface Physics Laboratory (ESPL) is currently developing new technologies that will further NASA's capabilities to colonize lunar and Martian environments. At the ESPL, the objective of the overall project is to aid in the dust mitigation of robotic and human exploration missions to the moon and Mars. The moon and Mars are covered with layers of dust, which can make long-term exploration missions very difficult. The team at the ESPL is developing an electrostatic precipitator (ESP) to aid in the reduction of interference from airborne Martian dust on equipment. The ESP is designed to mitigate the dust in an intake of CO2-rich dusty gas (i.e., the Martian atmosphere). The ESP is essentially a cylindrical tube with a coaxial wire electrode. Applying a high voltage through this electrode induces a corona discharge (a glowing plasma that envelops the electrode), which is used to charge the inflowing dust. The electric field caused by the corona pushes the charged dust to the walls of the precipitator, preventing the dust to flow out of the tube. Environmental dust can make long-term exploration missions very difficult, and settled dust is no exception. Settled lunar or Martian dust can hinder the performance and lifetime of equipment. For example, dust can settle on the solar panels of a lunar or Martian rover, decreasing its performance while increasing its charging time. To address this, the team at the ESPL is also developing an electrodynamic dust shield (EDS), which is designed to remove lunar or Martian dust from the surfaces of equipment. The EDS uses a non-uniform electric field to generate a dielectrophoretic force, which pushes the particles away from the surface of the shield. A number of dust shields will be tested on the exterior of the International Space Station (ISS) via MISSE-11, a flight payload to the ISS that will test the effects of long-term exposure to space on materials. During my internship at the ESPL, I aided in the development of these technologies. For the ESP, I helped characterize the electrical properties of various geometries and helped redesign the hardware of the testbed (the precipitator used to test this technology in the lab). To characterize the electrical properties of the ESP, I ran various tests of the precipitator, which consisted of varying the environmental conditions and geometry of the testbed. Analyzing the electrical properties of the ESP in various environmental conditions is necessary to characterize its collection efficiency, since it will be used in the dusty Martian environment. For the EDS, I helped analyze the dielectric strength of the surface of the shield via high-voltage testing. A dielectrically strong surface will help the shield survive the harsh environment of space, which will enable it to have both lunar and Martian applications

    Chemical characterization of ambient aerosol collected during the southwest monsoon and intermonsoon seasons over the Arabian Sea: Anions and cations

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    Ambient aerosol samples were collected over the northern Indian Ocean during two 1 month-long research cruises (German R/V Meteor) that took place during the intermonsoon (May) and SW monsoon (July/August) of 1995. A high volume and two small volume collectors were used to collect samples, which were subsequently analyzed for ferrous iron, 32 elements, and anions and cations. The present paper focuses on the bulk aerosol material, the ions, while utilizing some of the trace metal data that were presented in more detail in our previous paper [Siefert et al., 1999]. Data are analyzed and interpreted with the aid of principal component and multiple linear regression analyses. Intermonsoon samples were strongly influenced by continental material, both of crustal and anthropogenic origin. The crustal component (24.5±13% of the total suspended particulate mass (TSP), 6.0±4.4 μg m^(−3)) contained 3.2% gypsum (CaSO_4). While more than half of the TSP (21.2±9.6 μg m^(−3)) during the SW monsoon was sea-salt-derived due to the strong winds prevailing during this season, only 1.7±1.1% (0.7±0.4 μg m^(−3)) was found to be of crustal origin. Sulfate (SO_4^(2−)) sources were determined and quantified with linear regression analyses utilizing specific tracers for the independent variables. Lead (Pb) was found to be a more reliable surrogate for anthropogenic SO_4^(2−) compared to nitrate (NO_3^−) during the relatively polluted intermonsoon. Soluble calcium (Ca^(2+)) served as the tracer for gypsum, and methane sulfonate (MSA) served as the tracer for biogenically derived SO_4^(2−) during both seasons. On the basis of this analysis, 75% of the non-sea-salt sulfate (NSS-SO_4^(2−)) (0.8±0.2 μg m^(−3), representing ∼2.4% of TSP) was found to be of biogenic origin during the SW monsoon with the remaining 25% of anthropogenic origin. During the intermonsoon, NSS-SO_4^(2−) accounted for 2.1±1.2 μg m^(−3) (∼9.2% of TSP) and had a composition that was 65% anthropogenic, 21% biogenic, and 14% gypsum-derived. Linear regression analyses revealed that the bio-SO_4^(2−)/MSA weight ratios appear to be consistent with the temperature dependence proposed by Hynes et al. [1986]. In this case the yield of SO_4^(2−) increased relative to MSA with an increase in temperature. Three samples during the SW monsoon, near the coast of Oman, showed lower temperatures, due to coastal upwelling, than the rest of the samples; at 24°C the bio-SO_4^(2−)/MSA weight ratio was 6.8±0.5. The remainder of the SW monsoon samples were collected at an average temperature of 27.2°C, for which the bio-SO_4^(2−)/MSA weight ratio was 13.5±4.4. At an average temperature of 28.9°C during the intermonsoon, sampling gave a ratio of 17.7±4.8. These observations indicate a temperature dependence factor between 24° and 29°C of 2.2 (i.e., a 2.2 increase in the ratio of bio-SO_4^(2−)/MSA with every degree temperature increase). Cl− deficits determined during both seasons appear to indicate that different mechanisms may govern the observed depletion of Cl− in each season

    Chemical characterization of ambient aerosol collected during the southwest monsoon and intermonsoon seasons over the Arabian Sea: Labile-Fe(II) and other trace metals

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    Atmospheric deposition of iron (Fe) to certain regions of the oceans is an important nutrient source of Fe to the biota, and the ability of the biota to uptake Fe is dependent on the speciation of the Fe. Therefore understanding the speciation of Fe in the atmosphere is critical to understanding the role of Fe as a nutrient source in surface ocean waters. Labile ferrous iron (Fe(II)) concentrations as well as total concentrations for Fe and other important trace metals, cations, and anions were determined over the Arabian Sea for two nonconsecutive months during 1995. Ambient aerosol samples were collected during the Indian Ocean intermonsoon and southwest monsoon seasons over the Arabian Sea. Sampling took place aboard the German research vessel Meteor in the months of May (leg M32/3; intermonsoon) and July/August (leg M32/5; southwest monsoon). Both cruise tracks followed the 65th east meridian, traveling for 30 days each (from north to south during leg M32/3 and from south to north during leg M32/5). A high-volume dichotomous virtual impactor with an aerodynamic cutoff size of 3 μm was used to collect the fine and coarse aerosol fractions for metal analysis. A low volume collector was used to collect aerosol samples for anion and cation analysis. The analysis for labile-Fe(II) was done immediately after sample collection to minimize any possible Fe redox reactions which might occur during sample storage. The analytical procedure involved filter extraction in a formate/formic acid buffered solution at pH 4.2 followed by colorimetric quantification of soluble Fe(II). Metals, anions, and cations were analyzed after the cruise. Total atmospheric aqueous-labile-Fe(II) concentrations during the intermonsoon were between 4.75 and 80%) was present in the fine fraction (<3.0 μm). During the southwest monsoon, atmospheric aqueous-labile-Fe(II) concentrations were consistently below the detection limit (<0.34 to <0.089 ng m^(−3), depending on the volume of air sampled). Air mass back trajectories (5 day, three dimensional) showed that air masses sampled during the southwest monsoon had advected over the open Indian Ocean, while air masses sampled during the intermonsoon had advected over northeast Africa, the Saudi Arabian peninsula, and southern Asia. These calculations were consistent with the results of the statistical analysis performed on the data set which showed that the variance due to crustal species during the intermonsoon samples was greater than the variance due to crustal species during the southwest monsoon. The factor scores for the crustal components were also greater when the back trajectories had advected over the nearby continental masses. Principal component analysis was also performed with the intermonsoon samples where aqueous labile Fe(II) was above the detection limit. Aqueous labile Fe(II) did not correlate well with other species indicating possible atmospheric processing of the iron during advection

    Chemical composition of aerosols collected over the tropical North Atlantic Ocean

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    Ambient aerosol samples were collected over the tropical northern Atlantic Ocean during the month of April 1996 onboard the R/V Seward Johnson. Dichotomous high-volume collector samples were analyzed for ferrous iron immediately after collection, while trace metals, anions, and cations were determined upon return to the laboratory. Data are analyzed with the aid of enrichment factor, principal component, and weighted multiple linear regression analyses. Average mineral aerosol concentrations amounted to 19.3±16.4 μg m^(−3) whereby the chemical characteristics and air mass back trajectories indicated the dust to be of a typical shale composition and Saharan origin. Calcite accounted for 3.0 and 7.9% of the mineral aerosol during the first and second halves of the cruise, respectively. Total iron concentrations (averaging 0.84±0.61 μg m^(−3)) are crustally derived, of which 0.51±0.56% is readily released as Fe(II). Eighty-six percent of this Fe(II) is present in the fine (<3 μm diameter) aerosol fraction and correlates with NSS-SO_4^(2−) and oxalate. Approximately 23% of the measured NSS-SO_4^(2−) in both size fractions appears to be biogenically derived, and the rest is of anthropogenic nature. Biogenic SO_4^(2−) /methanesulfonic acid (MSA) ratios could not be easily extracted by employing a multiple linear regression analysis analogous to that of Johansen et al. [1999], possibly due to the varying characteristics of the aerosol chemistry and air temperature during the cruise. Because of the presence of anthropogenic SO_4^(2−), the non-sea-salt (NSS)- SO_4^(2−)/MSA ratio, 37.4±6.4, is elevated over what would be expected if the NSS - SO_4^(2−) were purely biogenic. Cl^− depletion is seen in all samples and averages 18.3±9.1%. The release of Cl from the aerosol phase appears to occur through acid displacement reactions with primarily HNO_3 in the coarse and H_2SO_4 in the fine fraction

    A Triboelectric Sensor Array for Electrostatic Studies on the Lunar Surface

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    The moons electrostatic environment requires careful consideration in the development of future lunar landers. Electrostatically charged dust was well documented during the Apollo missions to cause thermal control, mechanical, and visibility issues. The fine dust particles that make up the surface are electrostatically charged as a result of numerous charging mechanisms. The relatively dry conditions on the moon creates a prime tribocharging environment during surface operations. The photoelectric effect is dominant for lunar day static charging, while plasma electrons are the main contributor for lunar night electrostatic effects. Electrostatic charging is also dependent on solar intensity, Earth-moon relative positions, and cosmic ray flux. This leads to a very complex and dynamic electrostatic environment that must be studied for the success of long term lunar missions.In order to better understand the electrostatic environment of planetary bodies, Kennedy Space Center, in previous collaboration with the Jet Propulsion Laboratory, has developed an electrostatic sensor suite. One of the instruments included in this package is the triboelectric sensor array. It is comprised of strategically selected materials that span the triboelectric series and that also have previous spaceflight history. In this presentation, we discuss detailed testing with the triboelectric sensor array performed at Kennedy Space Center. We will discuss potential benefits and use cases of this low mass, low cost sensor package, both for science and for mission success

    Plant Communities of Highland Heights Community Park, Cuyahoga County, Ohio

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    Author Institution: Dept of Biological, Geological & Environmental Sciences, Cleveland State University, Cleveland, OHAuthor Institution: Dept of Biology, John Carroll University, University Heights, OHAuthor Institution: Normandeau Associates, Bedford, NHWe have described the vegetation structure with respect to various community types of Highland Heights Community Park and adjoining territory. High values of Shannon’s Diversity Indexes and Floristic Quality Assessment Indexes indicate a superior quality, species-rich habitat with several high-fidelity species. Based on our research, which reveals that the study site is worthy of conservation and preservation, we suggest recommendations to the city of Highland Heights for park management and land use planning
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