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Reaction mechanism of metastable peak formation on stainless steel cycloid envelope of mass spectrometer exposured to gaseous mixtures
A gas beam consisting of a mixture of atomic and molecular oxygen has been directed at the ion source of a mass spectrometer like those used in sounding rockets for determining the neutral composition of the lower thermosphere. The loss of atomic oxygen on mass spectrometer surfaces was evaluated by flagging the beam in several ways and comparing the experimental results with predicted values. The results obtained suggest that in rocket flights using similar instruments the atomic oxygen densities computed assuming no-loss conditions may be low by a factor of 2.5. Studies made using a beam containing tracer O-18 indicate that carbon dioxide observed when atomic oxygen enters the source is formed in a reaction involving atomic oxygen from the beam and carbon monoxide from the surfaces bombarded.
Introduction: The Ion Neutral Mass Spectrometer (INMS) aboard the Cassini orbiter has obtained the first in situ composition measurements of the neutral densities of molecular nitrogen, methane, argon, and a host of stable carbon-nitrile compounds in its first flyby of Titan. The bulk composition and thermal structure of the moon s upper atmosphere do not appear to be changed since the Voyager flyby in 1979. However, the more sensitive techniques provided by modern in-situ mass spectrometry also give evidence for large-spatial-scale large-amplitude atmospheric waves in the upper atmosphere and for a plethora of stable carbon-nitrile compounds above 1174 km. Furthermore, they allow the first direct measurements of isotopes of nitrogen, carbon, and argon, which provide interesting clues about the evolution of the atmosphere. The atmosphere was first accreted as ammonia and ammonia ices from the Saturn sub-nebula. Subsequent photochemistry likely converted the atmosphere into molecular nitrogen. The early atmosphere was 1.5 to 5 times more substantial and was lost via escape over the intervening 4.5 billion years due to the reduced gravity associated with the relatively small mass of Titan. Carbon in the form of methane has continued to outgas over time from the interior with much of it being deposited in the form of complex hydrocarbons on the surface and some of it also being lost to space.
The magnetic ion-mass spectrometer is designed to measure the abundances of the ambient positive ions in the ionosphere. It will be calibrated in flight against the retarding-potential analyzer and the cylindrical electrostatic probe to give absolute concentration data for the ion species detected. These parameters can be measured to approximately plus or minus 10% in well-behaved regions where concentrations are above 1000/cu cm. However, in highly structured polar regions, some degradation in accuracy may be expected. Three mass ranges, covered simultaneously by the scan of the instrument, 1 to 4, 4 to 16, and 16 to 64 amu, permit measurement of the entire mass range, 1 to 64 amu, in 1 sec in the main (peaks) mode. An alternate mode, analog-long, will extend the mass range to 90 amu with a 9-sec period.
Miniature, lightweight focal-plane magnetic sector of mass spectrometer (Mattauch-Herzog type) developed. Magnetic sector integral part of portable gas-chromatograph/mass spectrometer (GC/MS). Focal plane covers nominal range of 40 to 240 atomic mass units for 1-keV ion energy. System used for analyzing pollutants in field environments.
Recent experiments were conducted in Langley Research Center's molecular beam system to perform an absolute calibration of the lunar orbital mass spectrometer which was flown on the Apollo 15 and 16 missions. Tests were performed with several models of the instrument using two test gases, argon and neon, in the 1 ntorr to .1 picotorr range. Sensitivity to argon at spacecraft orbital velocity was .00028 A/torr enabling partial pressures in the .01-picotorr range to be measured at the spacecraft altitude. Neon sensitivity was nearly a factor of 5 less. Test data support the feasibility of using the lunar orbital mass spectrometer as a tool to gather information about the lunar atmosphere.
Purification of target holder and duoplasmatron ion source for solid mass spectrometer and spectrograph
Mass spectrometer pyrolysis of ammonium perchlorate at low pressure
Mass spectrometer leak testing by calibrated enclosure method for quantification of gaseous leaks in large complex systems
Explorer 31 ion mass spectrometer calibrated in flight and compared with Alouette 2 topside electron concentration data
Design and performance of breadboard miniaturized mass spectrometer for lunar mass probing
Ion microprobe mass spectrometer with cooled electrode target for analyzing traces of fluids
Computer controlled data handling system for quadrupole mass spectrometer performing on-line chemical analysis of rocket chamber combustion gases
Ion-mass-spectrometer measurements made, as part of the University of Iowa's Plasma Diagnostic Package, on the STS-3 and Spacelab 2 missions, sampled a variety of positive ion composition perturbations in response to gas emissions from the vehicle. A background of contaminant ion species (mostly relating to water) always exists in the vicinity of the Shuttle. The measured number fluxes of the contaminant ions vary differently from those of the ambient ions in response to changes in the spectrometer and spacecraft angles of attack. There is a near-Shuttle wake cavity in the contaminant ion distributions which has a different spatial configuration than the wake of the ambient ions. Although water dumps produce the longest term ion perturbations, the most well defined effects were observed from measurements taken during the short firings of the reaction-control-system thrusters.
The Giotto ion mass spectrometer high-intensity spectrometer (IMS-HIS) measured fluxes of ions from about 260,000 km before (1008:37 UT spacecraft time) to about 86,000 km after (1701:33 UT spacecraft time) closest approach to comet P/Grigg-Skjellerup during the encounter on July 10, 1992. Although the HIS sensor was not designed to measure protons, these ions were measured far from the comet. Close in to the comet, the ions observed were probably also protons, although heavier ions cannot be completely ruled out. Considerable temporal structure appears in the data, well-correlated with the data of other instruments onboard, especially those of the magnetometer. In particular, the ion count rate correlates with the direction of the magnetic field. This strong modulation at the water group ion cyclotron period (approx. 90 s) inside the inbound bow wave indicates a very narrow ion pitch angle distribution. Hence at Grigg-Skjellerup the ions appear to experience very little pitch angle scattering. This may result from strong compression in the rapidly increasing magnetic field.
The Giotto Ion Mass Spectrometer High Intensity Spectrometer (IMS-HIS) measured fluxes of ions from about 260,000 km before (10:08:37 UT spacecraft time) to about 86,000 km after (17:01:33 UT spacecraft time) closest approach to comet P/Grigg- Skjellerup during the encounter on July 10, 1992. Although the HIS sensor was not designed to measure protons, the unusual flyby geometry at Grigg-Skjellerup allowed the sensor to detect these ions. Considerable temporal structure appears in the data, well- correlated with the data of other instruments onboard, especially those of the magnetometer. In particular, the proton count rate correlates with the direction of the magnetic field.
The 2018 ExoMars rover mission includes the Mars Organic Molecule Analyzer (MOMA) investigation. MOMA will examine the chemical composition of samples acquired from depths of up to two meters below the martian surface, where organics may be protected from degradation derived from cosmic radiation and/or oxidative chemical reactions. When combined with the complement of instruments in the rover's Pasteur Payload, MOMA has the potential to reveal the presence of a wide range of organics preserved in a variety of mineralogical environments, and to begin to understand the structural character and potential origin of those compounds. The MOMA investigation is led by the Max Planck Institute for Solar System Research (MPS) with the mass spectrometer subsystem provided by NASA GSFC. MOMA's linear ion trap mass spectrometer (ITMS) is designed to analyze molecular composition of: (i) gas evolved from pyrolyzed powder samples and separated in a gas chromatograph; and, (ii) ions directly desorbed from crushed solid samples at Mars ambient pressure, as enabled by a pulsed UV laser system, fast-actuating aperture valve and capillary ion inlet. Breadboard ITMS and associated electronics have been advanced to high end-to-end fidelity in preparation for flight hardware delivery to Germany in 2015.
Science missions targeting the detection of organics from jet plumes originating from icy moons (i.e. Europa and Enceladus) will employ next-generation, state-of-the-art mass spectrometers to measure the composition of icy moon plume effluents and exospheres. During fly-bys, as mass spectrometers make their scientific measurements, molecular emissions from the spacecraft can interact with the local exosphere and associated jet plumes from the sub-surface oceans of the icy moons. Spacecraft-induced molecular effluents collide with molecules from the ambient exosphere, and a fraction of the spacecraft emissions are returned to the spacecraft and its complement of science instruments. The rate at which emitted molecules are returned to the spacecraft by collisions with other molecules (e.g. in Europa’s exosphere) is the return flux. The return flux of molecular emission from spacecraft sources is a major contributor to contaminant deposition onto the complement of contamination-sensitive instruments. Characterization of return flux is critical to the definition of requirements for materials outgassing for the spacecraft and its instruments, and for the definition of thruster operations.