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Lane, Arthur L.

Publications and source records attributed to Lane, Arthur L..

At least 19 records
All sourcesNASA NTRSDOE OSTI
NASA NTRS2018

Spectroscopic Chemical Analysis Methods and Apparatus

Spectroscopic chemical analysis methods and apparatus are disclosed which employ deep ultraviolet (e.g. in the 200 nm to 300 nm spectral range) electron beam pumped wide bandgap semiconductor lasers, incoherent wide bandgap semiconductor light emitting devices, and hollow cathode metal ion lasers to perform non-contact, non-invasive detection of unknown chemical analytes. These deep ultraviolet sources enable dramatic size, weight and power consumption reductions of chemical analysis instruments. In some embodiments, Raman spectroscopic detection methods and apparatus use ultra-narrow-band angle tuning filters, acousto-optic tuning filters, and temperature tuned filters to enable ultra-miniature analyzers for chemical identification. In some embodiments Raman analysis is conducted along with photoluminescence spectroscopy (i.e. fluorescence and/or phosphorescence spectroscopy) to provide high levels of sensitivity and specificity in the same instrument.

Hug, William F.↗
NASA NTRS2018

Native Fluorescence Detection Methods, Devices, and Systems for Organic Compounds

Naphthalene, benzene, toluene, xylene, and other volatile organic compounds VOCs have been identified as serious health hazards. Embodiments of the invention are directed to methods and apparatus for near-real-time in-situ detection and accumulated dose measurement of exposure to naphthalene vapor and other hazardous gaseous VOCs. The methods and apparatus employ excitation of fluorophors native or endogenous to compounds of interest using light sources emitting in the ultraviolet below 300 nm and measurement of native fluorescence emissions in distinct wavebands above the excitation wavelength. The apparatus of some embodiments are cell-phone-sized sensor/dosimeter "badges" to be worn by personnel potentially exposed to hazardous VOCs. The badge sensor of some embodiments provides both real time detection and data logging of exposure to naphthalene or other VOCs of interest from which both instantaneous and accumulated dose can be determined.

Hug, William F.↗
NASA NTRS2017

Spectroscopic Chemical Analysis Methods and Apparatus

Spectroscopic chemical analysis methods and apparatus are disclosed which employ deep ultraviolet (e.g. in the 200 nm to 300 nm spectral range) electron beam pumped wide bandgap semiconductor lasers, incoherent wide bandgap semiconductor light emitting devices, and hollow cathode metal ion lasers to perform non-contact, non-invasive detection of unknown chemical analytes. These deep ultraviolet sources enable dramatic size, weight and power consumption reductions of chemical analysis instruments. In some embodiments, Raman spectroscopic detection methods and apparatus use ultra-narrow-band angle tuning filters, acousto-optic tuning filters, and temperature tuned filters to enable ultra-miniature analyzers for chemical identification. In some embodiments Raman analysis is conducted along with photoluminescence spectroscopy (i.e. fluorescence and/or phosphorescence spectroscopy) to provide high levels of sensitivity and specificity in the same instrument.

Hug, William F.↗
NASA NTRS2016

Native Fluorescence Detection Methods, Devices, and Systems for Organic Compounds

Naphthalene, benzene, toluene, xylene, and other volatile organic compounds VOCs have been identified as serious health hazards. Embodiments of the invention are directed to methods and apparatus for near-real-time in-situ detection and accumulated dose measurement of exposure to naphthalene vapor and other hazardous gaseous VOCs. The methods and apparatus employ excitation of fluorophors native or endogenous to compounds of interest using light sources emitting in the ultraviolet below 300 nm and measurement of native fluorescence emissions in distinct wavebands above the excitation wavelength. The apparatus of some embodiments are cell-phone-sized sensor/dosimeter "badges" to be worn by personnel potentially exposed to hazardous VOCs. The badge sensor of some embodiments provides both real time detection and data logging of exposure to naphthalene or other VOCs of interest from which both instantaneous and accumulated dose can be determined.

Hug, William F.↗
NASA NTRS2014

Native Fluorescence Detection Methods and Detectors for Naphthalene and/or Other Volatile Organic Compound Vapors

Naphthalene, benzene, toluene, xylene, and other volatile organic compounds have been identified as serious health hazards. This is especially true for personnel working with JP8 jet fuel and other fuels containing naphthalene as well as other hazardous volatile organic compounds (VOCs). Embodiments of the invention are directed to methods and apparatus for near-real-time in-situ detection and accumulated dose measurement of exposure to naphthalene vapor and other hazardous gaseous VOCs. The methods and apparatus employ excitation of fluorophors native or endogenous to compounds of interest using light sources emitting in the ultraviolet below 300 nm and measurement of native fluorescence emissions in distinct wavebands above the excitation wavelength. The apparatus of some embodiments are cell-phone-sized sensor/dosimeter "badges" to be worn by personnel potentially exposed to naphthalene or other hazardous VOCs. The badge sensor of some embodiments provides both real time detection and data logging of exposure to naphthalene or other VOCs of interest from which both instantaneous and accumulated dose can be determined. The badges employ a new native fluorescence based detection method to identify and differentiate VOCs. The particular focus of some embodiments are the detection and identification of naphthalene while other embodiments are directed to detection and identification of other VOCs like aromatic hydrocarbons such as benzene, toluene, and xylene.

Hug, William F.↗
NASA NTRS2002

Science goals for a Mars Polar Cap subsurface mission : optical approaches for investiagations of inclusions in ice

The Mars Polar Caps are highly interesting features of Mars and have received much recent attention with new and exciting data on morphology, basal units, and layered outcroppings. We have examined the climatological, glaciological, and geological issues associated with a subsurface exploration of the Mars North Polar Cap and have determined that a finescale optical examination of ice in a borehole, to examine the stratigraphy, geochemistry and geochronology of the ice, is feasible. This information will enable reconstruction of the development of the cap as well as predication of the properties of its ice. We present visible imagery taken of dust inclusions in archived Greenland ice cores as well as in-situ images of accreted lithologic inclusions in West Antarctica, and we argue for use of this kind of data in Mars climate reconstruction as has been successful with Greenland and Antarctic ice core anlaysis.

dust↗
NASA NTRS2002

Science goals for a Mars Polar Cap subsurface mission : optical approaches for investigations of inclusions in ice

The Mars Polar Caps are highly interesting features of Mars and have received much recent attention with new and exciting data on morphology, basal units, and layered outcroppings. We have examined the climatological, glaciological, and geological issues associated with a subsurface exploration of the Mars North Polar Cap and have determined that a finescale optical examination of ice in a borehole, to examine the stratigraphy, geochemistry and geochronology of the ice, is feasible. This information will enable reconstruction of the development of the cap as well as prediction of the properties of its ice. We present visible imagery taken of dust inclusions in archived Greenland ice cores as well as in-situ images of accreted lithologic inclusions in West Antarctica, and we argue for use of this kind of data in Mars climate reconstruction as has been successful with Greenland and Antarctic ice core analysis. .

scattering↗
NASA NTRS2001

Mars Mineralogy by Microbeam Raman Spectrometry

The Mars Microbeam Raman Spectrometer, under development at Washington University and the Jet Propulsion Laboratory, can identify oxide, sulfide, and oxyanion minerals, bound water and OH, and organic and graphitic carbon in Mars rocks and soils in situ. Additional information is contained in the original extended abstract.

Haskin, Larry A.↗
NASA NTRS2000

The Athena Raman Spectrometer

Raman spectroscopy provides a powerful tool for in situ mineralogy, petrology, and detection of water and carbon. The Athena Raman spectrometer is a microbeam instrument intended for close-up analyses of targets (rock or soils) selected by the Athena Pancam and Mini-TES. It will take 100 Raman spectra along a linear traverse of approximately one centimeter (point-counting procedure) in one to four hours during the Mars' night. From these spectra, the following information about the target will extracted: (1) the identities of major, minor, and trace mineral phases, organic species (e.g., PAH or kerogen-like polymers), reduced inorganic carbon, and water-bearing phases; (2) chemical features (e.g. Mg/Fe ratio) of major minerals; and (3) rock textural features (e.g., mineral clusters, amygdular filling and veins). Part of the Athena payload, the miniaturized Raman spectrometer has been under development in a highly interactive collaboration of a science team at Washington University and the University of Alabama at Birmingham, and an engineering team at the Jet Propulsion Laboratory. The development has completed the brassboard stage and has produced the design for the engineering model.

Wang, Alian↗
NASA NTRS1997

Chemical Schemes for Surface Modification of Icy Satellites: A Road Map

The icy Galilean satellites of Jupiter are subject to magnetospheric plasma ion bombardment, which induces chemical changes within the ice. The possible detection of CO2 on the surface of Ganymede by the Galileo spacecraft makes for a more complicated chemistry and increases the number of chemical compounds that may then be present. We outline chemical schemes for the irradiation of pure and mixed ices H2O/CO2 and suggest species which observers may detect on Europa, Ganymede, and Callisto, such as C3O2, H2CO3, H2O2, CO3, HO2, CO, H2CO, CH2CO, as well as K2O, KOH, and SO3, from plasma implantation. Column abundances of compounds in the ice are calculated using a specified energy input and G values (yield per 100 eV).

Delitsky, Mona L.↗
NASA NTRS1997

Chemical Schemes for Surface Modification of Icy Satellites: A Road Map

The icy Galilean Satellites of Jupiter are subject to magnetospheric plasma ion bombardment which induces chemical changes within the ice. The possible detection of CO2 on the surface of Ganymede by the Galileo spacecraft makes for a more complicatred chemistry and increases the number of chemical compounds that may then be present.

Galileo↗
NASA NTRS1997

IUE's View of Callisto: Detection of an SO2 Absorption Correlated to Possible Torus Neutral Wind Alterations

Observations taken with the International Ultraviolet Explorer (IUE) detected a 0.28 micron absorption feature on Callisto's leading and Jupiter-facing hemispheres. This feature is similar to Europa's 0.28 micron feature, however it shows no correlation with magnetospheric ion bombardment. The strongest 0.28 micron signature is seen in the region containing the Valhalla impact. This absorption feature also shows some spatial correlation to possible neutral wind interactions, suggestive of S implantation (rather than S(sub x)) into Callisto's water ice surface, Indications of possible temporal variations (on the 10% level) are seen at other wavelengths between the 1984-1986 and the 1996 observations.

Lane, Arthur L.↗
NASA NTRS1993

The brightness of Jupiter's satellite Io following emergence from eclipse - Selected observations, 1981-1989

Io's brightness was monitored following emergence from eclipse by Jupiter on 14 occasions during the Jupiter apparitions from 1981 to 1989 and no instance is found of what has been called posteclipse brightening. If all the observations are averaged, a 2 percent effect cannot be ruled out; however, this effect is also the size of the rms errors of the summed data set. If condensation followed by sublimation of SO2 frost is hypothesized to be the mechanism which causes posteclipse brightening, then solar insolation alone may not be sufficient to remove an optically thick layer of SO2 frost in the time required to conform with the positive reports of posteclipse brightening in the literature. An additional source of energy is required, such as warming caused by the impact of magnetospheric particles as they dissipate the energy of their motion into Io's surface.

Nelson, Robert M.↗
NASA NTRS1991

Particle sizes of the Uranus delta ring's inner diffuse companion through comparison of RSS and PPS Voyager occultation data

In January, 1976, Voyager 2's photopolarimeter and UV spectrometer observed Delta Sagitarii and Beta Persei during their occultation by the Uranian delta ring. An inner diffuse companion of this ring was detected and found to have an average width of 12 km. By comparing the widths and equivalent depths of the two sets of data, it is established that the particles making the greatest contribution to the integrated opacities of the companion are of greater-than-several-cm sizes. The particles appear to be located away from the photopolarimetry edges, where there may be particles smaller than those observed elsewhere.

Hui, John↗
NASA NTRS1990

Temperature and thermal emissivity of the surface of Neptune's satellite Triton

Analysis of the preliminary results from the Voyager mission to the Neptune system has provided the scientific community with several methods by which the temperature of Neptune's satellite Triton may be determined. If the 37.5 K surface temperature reported by several Voyager investigations is correct, then the photometry reported by the imaging experiment on Voyager requires that Triton's surface have a remarkably low emissivity. Such a low emissivity is not required in order to explain the photometry from the photopolarimeter experiment on Voyager. A low emissivity would be inconsistent with Triton having a rough surface at the about 100-micron scale as might be expected given the active renewal processes which appear to dominate Triton's surface.

Nelson, Robert M.↗
NASA NTRS1990

Observations of Neptunian rings by Voyager Photopolarimeter Experiment

The Voyager Photopolarimeter Experiment detected the Neptunian rings 1989N1R and possibly 1989N2R. These rings were also photographed by the Voyager imaging cameras in August 1989. The firm detection of 1989N1R has an equivalent depth (the product of the radial width and mean normal optical depth) of 0.77 + or - 0.13 km, while a less certain detection of 1989N2R has an equivalent depth of 0.7 km + or - 0.2 km. Several statistical techniques were used to search for additional material in the Neptune ring system, and none was identified at a high confidence level.

Horn, Linda J.↗
NASA NTRS1989

Photometry from Voyager 2 - Initial results from the Neptunian atmosphere, satellites, and rings

Voyager 2 has performed photopolarimetric measurements for the planet, several of its satellites, and its ring system. The Great Dark Spot is noted to appear as a low-albedo region, while the bright companion appear to lie at a higher altitude than the Great Dark Spot. Triton's linear phase coefficients are consistent with a solid-surface object having high reflectivity; its rotational phase curve indicates two major compositional units at its surface. The deficiency of material in Neptune's ring system by comparison with that of Uranus may indicate the absence of a recent moon-shattering event.

Lane, Arthur L.↗