William B. Brinckerhoff
Goddard Space Flight Center
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Featured researches published by William B. Brinckerhoff.
Astrobiology | 2013
Robert T. Pappalardo; Steven D. Vance; Fran Bagenal; Bruce G. Bills; Diana L. Blaney; Donald D. Blankenship; William B. Brinckerhoff; J. E. P. Connerney; Kevin P. Hand; Tori M. Hoehler; J. S. Leisner; W. S. Kurth; M.A. McGrath; Michael T. Mellon; J. M. Moore; G. W. Patterson; Louise M. Prockter; D.A. Senske; B. E. Schmidt; Everett L. Shock; D.E. Smith; K.M. Soderlund
The prospect of a future soft landing on the surface of Europa is enticing, as it would create science opportunities that could not be achieved through flyby or orbital remote sensing, with direct relevance to Europas potential habitability. Here, we summarize the science of a Europa lander concept, as developed by our NASA-commissioned Science Definition Team. The science concept concentrates on observations that can best be achieved by in situ examination of Europa from its surface. We discuss the suggested science objectives and investigations for a Europa lander mission, along with a model planning payload of instruments that could address these objectives. The highest priority is active sampling of Europas non-ice material from at least two different depths (0.5-2 cm and 5-10 cm) to understand its detailed composition and chemistry and the specific nature of salts, any organic materials, and other contaminants. A secondary focus is geophysical prospecting of Europa, through seismology and magnetometry, to probe the satellites ice shell and ocean. Finally, the surface geology can be characterized in situ at a human scale. A Europa lander could take advantage of the complex radiation environment of the satellite, landing where modeling suggests that radiation is about an order of magnitude less intense than in other regions. However, to choose a landing site that is safe and would yield the maximum science return, thorough reconnaissance of Europa would be required prior to selecting a scientifically optimized landing site.
Astrobiology | 2017
Jorge L. Vago; Frances Westall; A. J. Coates; R. Jaumann; Oleg Korablev; Valérie Ciarletti; Igor Mitrofanov; Jean-Luc Josset; Maria Cristina De Sanctis; Jean-Pierre Bibring; Fernando Rull; Fred Goesmann; Harald Steininger; W. Goetz; William B. Brinckerhoff; Cyril Szopa; F. Raulin; Howell G. M. Edwards; Lyle G. Whyte; Alberto G. Fairén; John C. Bridges; Ernst Hauber; Gian Gabriele Ori; Stephanie C. Werner; D. Loizeau; Ruslan O. Kuzmin; Rebecca M. E. Williams; Jessica Flahaut; F. Forget; Daniel Rodionov
Abstract The second ExoMars mission will be launched in 2020 to target an ancient location interpreted to have strong potential for past habitability and for preserving physical and chemical biosignatures (as well as abiotic/prebiotic organics). The mission will deliver a lander with instruments for atmospheric and geophysical investigations and a rover tasked with searching for signs of extinct life. The ExoMars rover will be equipped with a drill to collect material from outcrops and at depth down to 2 m. This subsurface sampling capability will provide the best chance yet to gain access to chemical biosignatures. Using the powerful Pasteur payload instruments, the ExoMars science team will conduct a holistic search for traces of life and seek corroborating geological context information. Key Words: Biosignatures—ExoMars—Landing sites—Mars rover—Search for life. Astrobiology 17, 471–510.
Rapid Communications in Mass Spectrometry | 2012
Stephanie A. Getty; William B. Brinckerhoff; Timothy J. Cornish; Scott A. Ecelberger; Melissa Floyd
RATIONALE A miniature time-of-flight mass spectrometer measuring 20 cm in length has been adapted to demonstrate two-step laser desorption/ionization (LDI) in a compact instrument package for enhanced organics detection. Two-step LDI decouples the desorption and ionization processes, relative to traditional LDI, in order to produce low-fragmentation mass spectra of organic analytes. Tuning the UV ionization laser energy would allow control of the degree of fragmentation, which might enable better identification of constituent species. METHODS A reflectron time-of-flight mass spectrometer prototype was modified to allow a two-laser configuration, with IR (1064 nm) desorption followed by UV (266 nm) postionization. A relatively low ion extraction voltage of 5 kV was applied at the sample inlet. RESULTS The instrument capabilities and performance were demonstrated with analysis of a model polycyclic aromatic hydrocarbon, representing a class of compounds important to the fields of Earth and planetary science. Two-step laser mass spectrometry (L2MS) analysis of a model PAH, pyrene, was demonstrated, including molecular ion identification and the onset of tunable fragmentation as a function of ionizing laser energy. Mass resolution m/Δm = 380 at full width at half-maximum was achieved for gas-phase postionization of desorbed neutrals in this highly compact mass analyzer. CONCLUSIONS Achieving L2MS in a highly miniaturized instrument enables a powerful approach to the detection and characterization of aromatic organics in remote terrestrial and planetary applications. Tunable detection of molecular and fragment ions with high mass resolution, diagnostic of molecular structure, is possible on such a compact L2MS instrument. The selectivity of L2MS against low-mass inorganic salt interferences is a key advantage when working with unprocessed, natural samples, and a mechanism for the observed selectivity is proposed.
Proceedings of SPIE, the International Society for Optical Engineering | 2008
Todd King; Stephanie A. Getty; Patrick A. Roman; F. A. Herrero; Hollis H. Jones; Duncan M. Kahle; Bernard A. Lynch; George Suárez; William B. Brinckerhoff; Paul R. Mahaffy
We are implementing nano- and micro-technologies to develop a miniaturized electron impact ionization mass spectrometer for planetary science. Microfabrication technology is used to fabricate the ion and electron optics, and a carbon nanotube (CNT) cathode is used to generate the ionizing electron beam. Future NASA planetary science missions demand miniaturized, low power mass spectrometers that exhibit high resolution and sensitivity to search for evidence of past and present habitability on the surface and in the atmosphere of priority targets such as Mars, Titan, Enceladus, Venus, Europa, and short-period comets. Toward this objective, we are developing a miniature, high resolution reflectron time-of-flight mass spectrometer (Mini TOF-MS) that features a low-power CNT field emission electron impact ionization source and microfabricated ion optics and reflectron mass analyzer in a parallel-plate geometry that is scalable. Charged particle electrodynamic modeling (SIMION 8.0.4) is employed to guide the iterative design of electron and ion optic components and to characterize the overall performance of the Mini TOF-MS device via simulation. Miniature (< 1000 cm3) TOF-MS designs (ion source, mass analyzer, detector only) demonstrate simulated mass resolutions > 600 at sensitivity levels on the order of 10-3 cps/molecule N2/cc while consuming 1.3 W of power and are comparable to current spaceflight mass spectrometers. Higher performance designs have also been simulated and indicate mass resolutions ~1000, though at the expense of sensitivity and instrument volume.
Proceedings of SPIE, the International Society for Optical Engineering | 2008
Patrick A. Roman; William B. Brinckerhoff; Stephanie A. Getty; F. A. Herrero; R. Hu; Hollis H. Jones; Duncan M. Kahle; Todd King; Paul R. Mahaffy
Solar system exploration and the anticipated discovery of biomarker molecules is driving the development of a new miniature time-of-flight (TOF) mass spectrometer (MS). Space flight science investigations become more feasible through instrument miniaturization, which reduces size, mass, and power consumption. However, miniaturization of space flight mass spectrometers is increasingly difficult using current component technology. Micro electro mechanical systems (MEMS) and nano electro mechanical systems (NEMS) technologies offer the potential of reducing size by orders of magnitude, providing significant system requirement benefits as well. Historically, TOF mass spectrometry has been limited to large separation distances as ion mass analysis depends upon the ion flight path. Increased TOF MS system miniaturization may be realized employing newly available high speed computing electronics, coupled with MEMS and NEMS components. Recent efforts at NASA Goddard Space Flight Center in the development of a miniaturized TOF mass spectrometer with integral MEMS and NEMS components are presented. A systems overview, design and prototype, MEMS silicon ion lenses, a carbon nanotube electron gun, ionization methods, as well as performance data and relevant applications are discussed.
International Journal of Astrobiology | 2016
W. Goetz; William B. Brinckerhoff; Ricardo Arevalo; Caroline Freissinet; Stephanie A. Getty; D. P. Glavin; Sandra Siljeström; Arnaud Buch; Fabien Stalport; A. Grubisic; Xiang Li; V. Pinnick; Ryan M. Danell; F. H. W. Van Amerom; Fred Goesmann; Harald Steininger; Noël Grand; F. Raulin; Cyril Szopa; Uwe J. Meierhenrich; John Robert Brucato
This paper describes strategies to search for, detect, and identify organic material on the surface and subsurface of Mars. The strategies described include those applied by landed missions in the past and those that will be applied in the future. The value and role of ESAs ExoMars rover and of her key science instrument Mars Organic Molecule Analyzer (MOMA) are critically assessed.
ieee aerospace conference | 2013
William B. Brinckerhoff; Veronica T. Pinnick; Friso H. W. van Amerom; Ryan M. Danell; Ricardo Arevalo; Martina S. Atanassova; Xiang Li; Paul R. Mahaffy; Robert J. Cotter; Fred Goesmann; Harald Steininger
The 2018 joint ESA-Roscosmos ExoMars rover mission will seek the signs of past or present life in the near-surface environment of Mars. The rover will obtain samples from as deep as two meters beneath the surface and deliver them to an onboard analytical laboratory for detailed examination. The Mars Organic Molecule Analyzer (MOMA) investigation forms a core part of the sample analysis capability of ExoMars. Its top objective is to address the main “life signs” goal of the mission through detailed chemical analysis of the acquired samples. MOMA characterizes organic compounds in the samples with a novel dual ion source ion trap mass spectrometer (ITMS). The ITMS supports both pyrolysis-gas chromatography (pyr-GC) and Mars ambient laser desorption/ionization (LDI) analyses in an extremely compact package. Combined with the unprecedented depth sampling capability of ExoMars, MOMA affords a broad and powerful search for organics over a range of preservational environments, volatility, and molecular weight.
ieee aerospace conference | 2011
Nancy Janet Chanover; David A. Glenar; David Voelz; Xifeng Xiao; Rula Tawalbeh; Penelope J. Boston; William B. Brinckerhoff; Paul R. Mahaffy; Stephanie A. Getty; Inge Loes ten Kate; A. C. McAdam
We discuss the development of a miniature near-infrared point spectrometer, operating in the 1.7–4 mm region, based on acousto-optic tunable filter (AOTF) technology. This instrument may be used to screen and corroborate analyses of samples containing organic biomarkers or mineralogical signatures suggestive of extant or extinct organic material collected in situ from planetary surfaces. The AOTF point spectrometer will be paired with a laser desorption time-of-flight (LDTOF) mass spectrometer and will prescreen samples for evidence of volatile or refractory organics before the laser desorption step and subsequent mass spectrometer measurement. 1 2 We describe the prototype AOTF point spectrometer instrument and present laboratory analysis of geological samples of known astrobiological importance. An initial mineral and rock sample suite of planetary relevance was used in the laboratory for baseline testing. To this, we will add a complement of astrobiologically relevant biosignatures from a variety of well-characterized geomicrobial study sites. We also describe LDTOF analysis of kaolinite and serpentine specimens, which are both highly relevant to the Martian surface mineralogy and the aqueous history of the planet. The AOTF-LDTOF instrument pairing offers the powerful advantage of cross-checked chemical analyses of individual samples, which can reduce chemical and biological interpretation ambiguities.
ieee aerospace conference | 2015
Ricardo Arevalo; William B. Brinckerhoff; Friso H. W. van Amerom; Ryan M. Danell; Veronica Pinnick; Xiang Li; Stephanie A. Getty; Lars Hovmand; Andrej Grubisic; Paul R. Mahaffy; Fred Goesmann; Harald Steininger
The Mars Organic Molecule Analyzer (MOMA) investigation is a key astrobiology experiment scheduled to launch on the joint ESA-Roscosmos ExoMars 2018 rover mission. MOMA will examine the chemical composition of geological samples acquired from depths of up to two meters below the martian surface, where fragile organic molecules may be protected from destructive cosmic radiation and/or oxidative chemical reactions. The heart of the MOMA mass spectrometer subsystem (i.e., MOMA-MS) is a miniaturized linear ion trap (LIT) that supports two distinct modes of operation to detect: i) volatile and semi-volatile, low-to-moderate mass organics (≤500 Da) via pyrolysis coupled with gas chromatography mass spectrometry (pyr/GCMS); and, ii) more refractory, moderate-to-high mass compounds (up to 1000 Da) via laser desorption (LDMS) at ambient Mars pressures. Additionally, the LIT mass analyzer enables selective ion trapping via multi-frequency waveform ion excitation (e.g., stored waveform inverse Fourier transform, or SWIFT), and structural characterization of complex molecules using tandem mass spectrometry (MS/MS). A high-fidelity Engineering Test Unit (ETU) of MOMA-MS, including the LIT subassembly, dual-gun electron ionization source, micropirani pressure gauge, solenoid-driven aperture valve, redundant detection chains, and control electronics, has been built and tested at NASA GSFC under relevant operational conditions (pressure, temperature, etc.). Spaceflight qualifications of individual hardware components and integrated subassemblies have been validated through vibration, shock, thermal, lifetime, and performance evaluations. The ETU serves as a pathfinder for the flight model buildup, integration and test, as the ETU meets the form, fit and function of the flight unit that will be delivered to MPS in late 2015. To date, the ETU of MOMA-MS has been shown to meet or exceed all functional requirements, including mass range, resolution, accuracy, instrumental drift, and limit-of-detection specifications, thereby enabling the primary science objectives of the MOMA investigation and ExoMars 2018 mission.
ieee aerospace conference | 2012
Nancy Janet Chanover; Rula Tawalbeh; David A. Glenar; David Voelz; Xifeng Xiao; K. Uckert; Penelope J. Boston; Timothy J. Cornish; Scott A. Ecelberger; Stephanie A. Getty; William B. Brinckerhoff; Paul R. Mahaffy
We discuss the development of a miniature near-infrared point spectrometer, operating between 1.7-3.45 μm, based on acousto-optic tunable filter (AOTF) technology. This instrument may be used to screen and corroborate analyses of samples containing organic biomarkers or mineralogical signatures suggestive of extant or extinct organic material collected in situ from planetary surfaces. The AOTF point spectrometer will be paired with a laser desorption time-of-flight (LDTOF) mass spectrometer and will prescreen samples for evidence of volatile or refractory organics before the laser desorption step and subsequent mass spectrometer measurement. We describe the AOTF point spectrometer instrument and present laboratory analysis of geological samples of known astrobiological importance. We also present LDTOF spectra of the same samples analyzed with the AOTF, which highlights the value of a comparative data set with the two instruments. We discuss plans for the integration of the two instruments, which is scheduled to take place in the first half of 2012. The AOTF-LDTOF instrument pairing offers the powerful advantage of cross-checked chemical analyses of individual samples, which can reduce chemical and biological interpretation ambiguities.