Engineering Papers⌕ Search

Engineering topics

Hoffman, J. H.

Publications and source records attributed to Hoffman, J. H..

At least 19 records
All sourcesNASA NTRSDOE OSTI
NASA NTRS2010

Carbon and Oxygen Stable Isotope Measurements of Martian Atmospheric CO2 by the Phoenix Lander

Precise stable isotope measurements of the CO2 in the martian atmosphere have the potential to provide important constraints for our understanding of the history of volatiles, the carbon cycle, current atmospheric processes, and the degree of water/rock interaction on Mars [1]. The isotopic composition of the martian atmosphere has been measured using a number of different methods (Table 1), however a precise value (<1%) has yet to be achieved. Given the elevated Delta(sup 13)C values measured in carbonates in martian meteorites [2-4] it has been proposed that the martian atmosphere was enriched in 13C [8]. This was supported by measurements of trapped CO2 gas in EETA 79001[2] which showed elevated Delta(sup 13)C values (Table 1). More recently, Earth-based spectroscopic measurements of the martian atmosphere have measured the martian CO2 to be depleted in C-13 relative to CO2 in the terrestrial atmosphere[ 7, 9-11]. The Thermal and Evolved Gas Analyzer (TEGA) instrument on the Mars Phoenix Lander [12] included a magnetic-sector mass spectrometer (EGA) [13] which had the goal of measuring the isotopic composition of martian atmospheric CO2 to within 0.5%. The mass spectrometer is a miniature instrument intended to measure both the martian atmosphere as well as gases evolved from heating martian soils.

Niles, Paul B.↗
NASA NTRS1998

Exploration of the Moon with Remote Sensing, Ground-Penetrating Radar, and the Regolith-Evolved Gas Analyzer (REGA)

There are two important reasons to explore the Moon. First, we would like to know more about the Moon itself: its history, its geology, its chemistry, and its diversity. Second, we would like to apply this knowledge to a useful purpose. namely finding and using lunar resources. As a result of the recent Clementine and Lunar Prospector missions, we now have global data on the regional surface mineralogy of the Moon, and we have good reason to believe that water exists in the lunar polar regions. However, there is still very little information about the subsurface. If we wish to go to the lunar polar regions to extract water, or if we wish to go anywhere else on the Moon and extract (or learn) anything at all, we need information in three dimensions an understanding of what lies below the surface, both shallow and deep. The terrestrial mining industry provides an example of the logical steps that lead to an understanding of where resources are located and their economic significance. Surface maps are examined to determine likely locations for detailed study. Geochemical soil sample surveys, using broad or narrow grid patterns, are then used to gather additional data. Next, a detailed surface map is developed for a selected area, along with an interpretation of the subsurface structure that would give rise to the observed features. After that, further sampling and geophysical exploration are used to validate and refine the original interpretation, as well as to make further exploration/ mining decisions. Integrating remotely sensed, geophysical, and sample datasets gives the maximum likelihood of a correct interpretation of the subsurface geology and surface morphology. Apollo-era geophysical and automated sampling experiments sought to look beyond the upper few microns of the lunar surface. These experiments, including ground-penetrating radar and spectrometry, proved the usefulness of these methods for determining the best sites for lunar bases and lunar mining operations.

Cooper, B. L.↗
NASA NTRS1986

Angular and energy distribution of low energy cometary ions measured in the outer coma of Comet Halley

During the early phase of the Giotto encounter with comet Halley, at distances from the nucleus greater than 350,000 km, the neutral mass spectrometer was operated in a mode allowing the measurement of low energy ions. Data reveal two important features of the outer coma: the presence of a sharp discontinuity in the plasma flow at 550,000 km from the nucleus which results in a significant decrease of the plasma flow accompanied by an increase in temperature; and the detection of newly born ions identified as O(+) and CO(+), at distances from the comet greater than 800,000 km.

Berthelier, J. J.↗
NASA NTRS1986

Evidence for HCS(+) and CH2SH(+) in the inner coma of Comet Halley

Number densities for ion species with masses 44, 45, and 47 amu/q were derived from ram energy spectra of the neutral gas mass spectrometer experiment on Giotto in the inner coma of comet Halley. The relative abundances of the masses suggest the presence of the ions CS(+), HCS(+), and CH2SH(+).

Krankowsky, D.↗
NASA NTRS1986

The D/H ratio in water from Halley

The neutral gas mass spectrometer on Giotto made neutral and ion composition measurements with a high mass resolution. Evaluation of the ion data within the contact surface gives a D/H ratio in water from Halley between 0.00006 and 0.00048. While this ratio is definitely not compatible with the D/H in molecular hydrogen of the protosolar nebula or the Jovian and Saturnian atmospheres, it is in the range observed for hydrogen in solar system objects which acquired their hydrogen as part of volatile molecules, e.g., as ices.

Eberhardt, P.↗
NASA NTRS1984

Ionospheric chemistry of NO(+)

An investigation is described of the behavior of NO(+) in the daytime F region, with basic ion concentration measurements from the Atmosphere Explorer C satellite. The data set was acquired along select orbits at low latitudes and exhibits substantial variations in the NO(+) concentration, both along and between nearby orbits. An excellent consistency is demonstrated between these observations and current chemical equilibrium theory, in contrast to differences that have been reported for the related N2(+) ion. Large variations in the concurrently observed electron temperature permit a relevant comparison between different laboratory determinations of the dissociative recombination rate coefficient. Contributions to the NO(+) production from several secondary sources are also evaluated. Results strengthen the basis for the current theoretical ionospheric chemistry of NO(+) and establish important constraints on resolution of the difficulties with N2(+).

Breig, E. L.↗
NASA NTRS1983

Photochemistry of N2(+) in the daytime F region

The photochemistry of N2(+) in the daytime F region continues to be a source of concern due primarily to the uncertain roles of the metastable O+(2D) ion and possible vibrational excitation. This investigation adopts a unique subset of data from the Atmospheric Explorer C satellite that spans distinct regions near the low-latitude F peak wherein either chemical reactions or electron processes alternatively control the N2(+) abundances. Concentrations of N2(+) calculated according to current theory and including recent laboratory data for O+(2D) losses via N2 are found to exceed ionospheric observations between 220 and 400 km by a factor near 2. Relevant characteristics of the basic molecular ion concentration measurements are described, along with an analysis for select orbits conducted according to current photochemical equilibrium theory. Possible simple modifications of this theory are discussed in terms of the constraints suggested by the nature of the observations.

Breig, E. L.↗
NASA NTRS1982

Magnetic deflection ion mass spectrometer experiment for atmosphere explorer

The magnetic ion mass spectrometer was carried aboard Atmosphere Explorer C and Atmosphere Explorer D. The instrument measures the relative abundance of ionic species with very high sensitivity and very high mass resolution. Thus isotopic ratios for various ion species can be examined and minor ion species such as O(++), N(++), and H(+) can be detected when their relative abundance is very small. These instruments functioned with no critical internal failures but the premature loss of the AE-D spacecraft after only a few months of operation has led to an emphasis of scientific achievement from AE-C. The very long lifetime of AE-C coupled with the prolonged time that this spacecraft spent near the F-region peak led to the accumulation of very large count numbers in the channeltron detectors.

Hoffman, J. H.↗
NASA NTRS1982

Venus was wet - A measurement of the ratio of deuterium to hydrogen

The deuterium-hydrogen abundance ratio in the Venus atmosphere was measured while the inlets to the Pioneer Venus large probe mass spectrometer were coated with sulfuric acid from Venus' clouds. The ratio is 0.016 + or - 0.002. The hundredfold enrichment of deuterium means that at least 0.3 percent of a terrestrial ocean was outgassed on Venus, but is consistent with a much greater production.

Donahue, T. M.↗
NASA NTRS1982

Instrument manual for the retarding ion mass spectrometer on Dynamics Explorer-1

The retarding ion mass spectrometer (RIMS) for Dynamics Explorer-1 is an instrument designed to measure the details of the thermal plasma distribution. It combines the ion temperature determining capability of the retarding potential analyzer with the compositional capabilities of the mass spectrometer and adds multiple sensor heads to sample all directions relative to the spacecraft ram direction. This manual provides a functional description of the RIMS, the instrument calibration, and a description of the commands which can be stored in the instrument logic to control its operation.

Fields, S. A.↗
NASA NTRS1982

Study of outgassing and decomposition of space shuttle heat protection tiles, fillers and adhesive

The purpose of this project was to determine the chemicals desorbing from the space shuttle heat protection tiles. The original protocol for this project involved direct insertion probe mass spectrometry (DIPMS) analysis of the outgassing products from the tiles. However, this method proved unsatisfactory due to the large number of compounds desorbing from the tiles. A purge and trap technique was then employed to collect and separate the chemicals desorbing from the tiles. The maximum temperature in this analysis was 180 C which is the gas chromatograph fused silica capillary column's temperature limit. The desorption was also carried out at atmospheric pressure with helium as the purge gas. A description of the modified protocol is given. All compounds are tentatively identified.

Proctor, B. L.↗
NASA NTRS1981

The Retarding Ion Mass Spectrometer on Dynamics Explorer-A

The thermal component of the magnetospheric plasma plays a key role in magnetosphere-ionosphere coupling processes, acting as a strong influence on ionospheric structure at low altitudes and as a source and modifier of the hotter plasma population at high altitudes. The Retarding Ion Mass Spectrometer (RIMS) instrument on Dynamics Explorer-A is designed to measure this important thermal plasma component. Using a combination of retarding potential analysis and magnetic ion mass spectrometer techniques, the RIMS instrument will measure the bulk plasma parameters of ion density (0.1 to 1,000,000 ions/cu cm), temperature (0-45 eV), and bulk flow (greater than 0.5 km/sec) in the inner plasmasphere and ionosphere, and the specific ion pitch angle and energy spectral characteristics in the outer plasmasphere and plasma trough for a mass range of 1-32 amu. The energy and mass spectral step sequences, as well as the multiplexing of the resultant data, can be tailored to accomplish a variety of thermal ion measurements throughout the inner magnetosphere.

Chappell, C. R.↗
NASA NTRS1981

Ion sputtering from satellite surfaces

The manifestations of the induced surface currents as observed by the magnetic ion mass spectrometer (MIMS) and retarding potential analyzer (RPA) instruments on AE-C and AE-D are described. Data from these instruments are used to infer the source of some of the different secondary ions observed, as well as their time history and emission energy. It is noted that the emitted particles have a characteristic energy of approximately 1 eV in the spacecraft frame of reference and lack the normal ram energy possessed by the ambient ions. Alkali ions Na(+) and K(+), in addition to nonionospheric NO(+) and O2(+), are observed at low altitudes. With the exception of NO(+), all these are thought to be released by impacts of neutral N2 or O2 with the surfaces. These ion currents decrease with a time constant of about six weeks for the alkali and four weeks for the O2 ions.

Hanson, W. B.↗
NASA NTRS1981

Continuation of data analysis from the ion mass spectrometer on the ISIS-2 spacecraft

The spectrometer measures the composition and number density of the positive ion species in the ionosphere as well as the ion flux normal to the spacecraft trajectory. The measurement of high latitude ionospheric dynamics is reported. Plans for an empirical composition model of the polar ionosphere at 1400 km altitude consisting of maps of the major constituent are also reported.

Hoffman, J. H.↗
NASA NTRS1981

Analysis of data from the Pioneer Venus Sounder Probe mass spectrometer

The composition of the lower atmosphere of the planet Venus from 62 km to the surface was measured by a neutral gas mass spectrometer onboard of the Pioneer Venus Sounder Probe. Fifty-one mass spectra were obtained with an average altitude resolution of approximately 1 km. The instrument measured the composition of the gases relative to CO2, the dominant gas, that is sampled from the Venus atmosphere through a special leak. The mass range extended from 1 to 208 amu with a sensitivity of the order of 1 ppm relative to CO2, but for the noble gases it was nearly 100 times better. A description of the instrument and the initial results are reported.

Hoffman, J. H.↗
NASA NTRS1981

Krypton and xenon in the atmosphere of Venus

The paper reports a determination by the Pioneer Venus large probe neutral mass spectrometer of upper limits to the concentration of krypton and xenon along with most of their isotopes in the atmosphere of Venus. The upper limit to the krypton mixing ratio is estimated at 47 ppb, with a very conservative estimate at 69 ppb. The probable upper limit to the sum of the mixing ratios of the isotopes Xe-128, Xe-129, Xe-130, Xe-131, and Xe-132 is 40 ppb by volume, with a very conservative upper limit three times this large.

Donahue, T. M.↗
NASA NTRS1981

The retarding ion mass spectrometer on dynamics Explorer-A

An instrument designed to measure the details of the thermal plasma distribution combines the ion temperature-determining capability of the retarding potential analyzer with the compositional capabilities of the mass spectrometer and adds multiple sensor heads to sample all directions relative to the spacecraft ram directions. The retarding ion mass spectrometer, its operational modes and calibration are described as well as the data reduction plan, and the anticipated results.

Chappell, C. R.↗