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Mars Solar Balloon Landed Gas Chromatograph Mass SpectrometerA Mars surface lander Gas Chromatograph Mass Spectrometer (GCMS) is described to measure the chemical composition of abundant and trace volatile species and isotope ratios for noble gases and other elements. These measurements are relevant to the study of atmospheric evolution and past climatic conditions. A Micromission plan is under study where a surface package including a miniaturized GCMS would be delivered to the surface by a solar heated hot air balloon based system. The balloon system would be deployed about 8 km above the surface of Mars, wherein it would rapidly fill with Martian atmosphere and be heated quickly by the sun. The combined buoyancy and parachuting effects of the solar balloon result in a surface package impact of about 5 m/sec. After delivery of the package to the surface, the balloon would ascend to about 4 km altitude, with imaging and magnetometry data being taken for the remainder of the daylight hours as the balloon is blown with the Martian winds. Total atmospheric entry mass of this mission is estimated to be approximately 50 kg, and it can fit as an Ariane 5 piggyback payload. The GCMS would obtain samples directly from the atmosphere at the surface and also from gases evolved from solid phase material collected from well below the surface with a Sample Acquisition and Transport Mechanism (SATM). The experiment envisioned in the Mars Micromission described would obtain samples from a much greater depth of up to one meter below the surface, and would search for organic molecules trapped in ancient stratified layers well below the oxidized surface. Insitu instruments on upcoming NASA missions working in concert with remote sensing measurement techniques have the potential to provide a more detailed investigation of mineralogy and the extent of simple volatiles such as CO2 and H2O in surface and subsurface solid phase materials. Within the context of subsequent mission opportunities such as those provided by the Ariane 5 piggyback payload based Micromissions, it is essential to implement an even broader chemical analysis and to enable a significant extension of previous isotope measurements. Such a development would enhance the presently very active study of questions of atmospheric evolution and loss and past climatic conditions. The method selected to implement this program can be based on well-established mass spectrometry techniques. Sampled gas is chemically and physically processed to separate the gas mixture into components using gas chromatograph and related enrichment techniques. This allows trace species to be identified and reveals isotopic distributions in many cases with improved precision. Samples of interest, such as organic molecules, may lie deep below the highly oxidized surface layer and the suggested program includes enhanced sampling techniques to measure volatiles preserved in solid phase material deep below the surface as well as gas from the well mixed atmosphere.
Document ID
19990027018
Acquisition Source
Goddard Space Flight Center
Document Type
Other
Authors
Mahaffy, P.
(NASA Goddard Space Flight Center Greenbelt, MD United States)
Harpold, D.
(NASA Goddard Space Flight Center Greenbelt, MD United States)
Niemann, H.
(NASA Goddard Space Flight Center Greenbelt, MD United States)
Atreya, S.
(Michigan Univ. Ann Arbor, MI United States)
Gorevan, S.
(Honeybee Robotics Ltd. New York, NY United States)
Israel, G.
(Centre National de la Recherche Scientifique Verrieres-Le Buisson, France)
Bertaux, J. L.
(Centre National de la Recherche Scientifique Verrieres-Le Buisson, France)
Jones, J.
(Jet Propulsion Lab., California Inst. of Tech. Pasadena, CA United States)
Owen, T.
(Hawaii Univ. Honolulu, HI United States)
Raulin, F.
(Paris Univ. Creteil, France)
Date Acquired
August 19, 2013
Publication Date
January 1, 1999
Subject Category
Instrumentation And Photography
Meeting Information
Meeting: Mars Exploration Programme and Sample Return Missions Symposium
Location: Paris
Country: France
Start Date: February 1, 1999
End Date: May 1, 1999
Distribution Limits
Public
Copyright
Work of the US Gov. Public Use Permitted.
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