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At least 55 records · Page 3

Sensitivity of Hollow Fiber Spacesuit Water Membrane Evaporator Systems to Potable Water Constituents, Contaminants and Air Bubbles

The Spacesuit Water Membrane Evaporator (SWME) is the baseline heat rejection technology selected for development for the Constellation lunar suit. The first SWME prototype, designed, built, and tested at Johnson Space Center in 1999 used a Teflon hydrophobic porous membrane sheet shaped into an annulus to provide cooling to the coolant loop through water evaporation to the vacuum of space. This present study describes the test methodology and planning and compares the test performance of three commercially available hollow fiber materials as alternatives to the sheet membrane prototype for SWME, in particular, a porous hydrophobic polypropylene, and two variants that employ ion exchange through non-porous hydrophilic modified Nafion. Contamination tests will be performed to probe for sensitivities of the candidate SWME elements to ordinary constituents that are expected to be found in the potable water provided by the vehicle, the target feedwater source. Some of the impurities in potable water are volatile, such as the organics, while others, such as the metals and inorganic ions are nonvolatile. The non-volatile constituents will concentrate in the SWME as evaporated water from the loop is replaced by the feedwater. At some point in the SWME mission lifecycle as the concentrations of the non-volatiles increase, the solubility limits of one or more of the constituents may be reached. The resulting presence of precipitate in the coolant water may begin to plug pores and tube channels and affect the SWME performance. Sensitivity to macroparticles, lunar dust simulant, and air bubbles will also be investigated.

Bue, Grant C.

A Model of Reduced Kinetics for Alkane Oxidation Using Constituents and Species for N-Heptane

The reduction of elementary or skeletal oxidation kinetics to a subgroup of tractable reactions for inclusion in turbulent combustion codes has been the subject of numerous studies. The skeletal mechanism is obtained from the elementary mechanism by removing from it reactions that are considered negligible for the intent of the specific study considered. As of now, there are many chemical reduction methodologies. A methodology for deriving a reduced kinetic mechanism for alkane oxidation is described and applied to n-heptane. The model is based on partitioning the species of the skeletal kinetic mechanism into lights, defined as those having a carbon number smaller than 3, and heavies, which are the complement of the species ensemble. For modeling purposes, the heavy species are mathematically decomposed into constituents, which are similar but not identical to groups in the group additivity theory. From analysis of the LLNL (Lawrence Livermore National Laboratory) skeletal mechanism in conjunction with CHEMKIN II, it is shown that a similarity variable can be formed such that the appropriately non-dimensionalized global constituent molar density exhibits a self-similar behavior over a very wide range of equivalence ratios, initial pressures and initial temperatures that is of interest for predicting n-heptane oxidation. Furthermore, the oxygen and water molar densities are shown to display a quasi-linear behavior with respect to the similarity variable. The light species ensemble is partitioned into quasi-steady and unsteady species. The reduced model is based on concepts consistent with those of Large Eddy Simulation (LES) in which functional forms are used to replace the small scales eliminated through filtering of the governing equations; in LES, these small scales are unimportant as far as the overwhelming part of dynamic energy is concerned. Here, the scales thought unimportant for recovering the thermodynamic energy are removed. The concept is tested by using tabular information from the LLNL skeletal mechanism in conjunction with CHEMKIN II utilized as surrogate ideal functions replacing the necessary functional forms. The test reveals that the similarity concept is indeed justified and that the combustion temperature is well predicted, but that the ignition time is over-predicted, a fact traced to neglecting a detailed description of the processes leading to the heavies chemical decomposition. To palliate this deficiency, functional modeling is incorporated into this conceptual reduction in addition to the modeling the evolution of the global constituent molar density, the enthalpy evolution of the heavies, the contribution to the reaction rate of the unsteady lights from other light species and from the heavies, the molar density evolution of oxygen and water, and the mole fractions of the quasisteady light species. The model is compact in that there are only nine species-related progress variables. Results are presented showing the performance of the model for predicting the temperature and species evolution. The model reproduces the ignition time over a wide range of equivalence ratios, initial pressure, and initial temperature.

Harstad, Kenneth G.

International Space Station Major Constituent Analyzer On-Orbit Performance

The Major Constituent Analyzer (MCA) is an integral part of the International Space Station (ISS) Environmental Control and Life Support System (ECLSS). The MCA is a mass spectrometer-based instrument designed to provide critical monitoring of six major atmospheric constituents; nitrogen, oxygen, hydrogen, carbon dioxide, methane, and water vapor. These gases are sampled continuously and automatically in all United States On-Orbit Segment (USOS) modules via the Sample Distribution System (SDS). The MCA is the primary tool for management of atmosphere constituents and is therefore critical for ensuring a habitable ISS environment during both nominal ISS operations and campout EVA preparation in the Airlock. The MCA has been in operation in the US Destiny Laboratory Module for over 10 years, and a second MCA has been delivered to the ISS for Node 3 operation. This paper discusses the performance of the MCA over the two past year, with particular attention to lessons learned regarding the operational life of critical components. Recent data have helped drive design upgrades for a new set of orbit-replaceable units (ORUs) currently in production. Several ORU upgrades are expected to increase expected lifetimes and reliability.

Gardner, Ben D.

Achieving ICME with Multiscale Modeling: The Effects of Constituent Properties and Processing on the Performance of Laminated Polymer Matrix Composite Structures

Integrated computational materials engineering (ICME) is a useful approach for tailoring the performance of a material. For fiber-reinforced composites, not only do the properties of the constituents of the composite affect the performance, but so does the architecture (or microstructure) of the constituents. The generalized method of cells is demonstrated to be a viable micromechanics tool for determining the effects of the microstructure on the performance of laminates. The micromechanics is used to predict the inputs for a macroscale model for a variety of different fiber volume fractions, and fiber architectures. Using this technique, the material performance can be tailored for specific applications by judicious selection of constituents, volume fraction, and architectural arrangement given a particular manufacturing scenario

computational mechanics

Interaction of 25 eV electrons with DNA constituents: XPS analysis of calf thymus DNA, nucleosides, and nucleobases

Abstract Understanding the interactions of secondary electrons generated by ionizing radiation provides a fundamental basis for developing strategies in cancer therapy. In this study, we investigated the interactions of 25 eV low-energy electrons (LEEs) with calf thymus DNA and its constituents, four types of nucleosides and nucleobases, using X-ray photoelectron spectroscopy (XPS). Based on the acquisition and analysis of core-level spectra (O 1s, C 1s, N 1s, and P 2p) in DNA, structural changes induced by 25 eV electrons suggest potential site- and base-specific selectivity. These changes may involve hydroxyl (C–OH) group release from the sugar moiety, cleavage of C–N bonds (likely corresponding to N-glycosidic linkages), and phosphate backbone damage in calf thymus DNA. Among the four nucleosides, thymidine and guanosine showed more evident structural modifications, while cytidine and adenosine were relatively stable. In addition, nucleosides displayed greater susceptibility to LEE-induced structural changes than their corresponding nucleobases. This study reveals the selective damage mechanisms of LEEs on various DNA constituents, which may provide mechanistic insights for future developments in precision cancer therapy based on molecular-level damage. Graphical abstract

Pereira-da-Silva, João (ORCID:0000000220661303)

Seasonal effects on distributions of minor neutral constituents in the mesosphere and lower thermosphere.

Calculations have been made of the diurnal variations in minor neutral constituents in the mesosphere and lower thermosphere for the condition of 60 deg latitude, summer and winter. Excited molecular oxygen has been added, and the effects of absorption of Schumann-Runge bands have been taken into account. The results show significant seasonal differences, which may be interpreted mainly in terms of the difference of penetration of solar radiation and the duration of sunlit hours. However, the comparison of the observed seasonal and diurnal variations in the airglow emissions from hydroxyl, atomic oxygen (5577 A), and excited molecular oxygen with those calculated from models suggests that effects of large-scale meridional circulation (horizontal and vertical transports) may be important in explaining these observations. It is shown that the concentration of the constituents whose main loss mechanism is recombination with atomic oxygen decreases sharply above 80 km.

Shimazaki, T.

Mass spectrometric analysis of organic compounds, water and volatile constituents in the atmosphere and surface of Mars - The Viking Mars Lander.

An experiment centering around a mass spectrometer is described, which is aimed at the identification of organic substances present in the top 10 cm of the surface of Mars and an analysis of the atmosphere for major and minor constituents as well as isotopic abundances. In addition, an indication of the abundance of water in the surface and some information concerning the mineralogy can be obtained by monitoring the gases produced upon heating the soil sample. The organic material will simply be expelled by heating to 150, 300, and 500 C into the carrier gas stream of a gas chromatograph interfaced to the mass spectrometer or by slowly heating the sample in direct communication with the spectrometer. It is planned to analyze a total of up to nine soil samples in order to study diurnal and seasonal variations. The system is designed to give useful data even for minor constituents if the total of organics should be as low as 5 ppm. The spectrometer covers the mass range of 12-200 with adequate resolution.

Anderson, D. M.

Minor constituents in the stratosphere and mesosphere

This paper is a brief survey of a portion of the research on trace constituents in the stratosphere and mesosphere between 1971 and 1974. A primary motivation for much of the stratospheric research came from the realization that man's activities may influence global climate and the atmospheric ozone content, our shield against certain UV wavelengths. A great deal of progress has been reported in understanding both the present background stratosphere and the responses to be expected from additions of nitrogen oxides, water, and chlorine oxides, especially with respect to ozone. Trace constituents in the mesosphere have been modeled and measured to increase our understanding of the physics and chemistry of the mesosphere but also to relate mesospheric composition and transport to ionospheric processes at higher altitudes, to D region ion chemistry, and to upper stratospheric composition.

Cicerone, R. J.

Measurements of trace constituents from atmospheric infrared emission and absorption spectra, a feasibility study

The feasibility of detecting eight trace constituents (CH4, HCl, HF, HNO3, NH3, NO, NO2 and SO2) against the rest of the atmospheric background at various altitudes from infrared emission and absorption atmospheric spectra was studied. Line-by-line calculations and observational data were used to establish features that can be observed in the atmospheric spectrum due to each trace constituent. Model calculations were made for experimental conditions which approximately represent state of the art emission and absorption spectrometers.

Goldman, A.

Experimental study of the constituents of space wash water

Data are presented that quantify some of the various constituents of human origin that may be expected in space wash water. The experiments were conducted under controlled conditions with a simulated crew of two male and two female subjects. The data show that the expected wash water constituents originating from human secretions are substantially lower than theoretical projections have indicated. Average daily quantities as well as individual extremes are given for both shower and laundry water. In addition, concentrations are presented for a projected model of wash water usage in a space station.

Colombo, G. V.

Airborne infrared interferometric observations and analysis of stratospheric trace constituents

Infrared interferometric observations of key trace constituents of the stratosphere have been obtained. The NASA Lear Airborne Observatory with the Grumman airborne interferometer system was flown in the lower stratosphere at an altitude of 13.7 km to obtain transmission spectra in the 2800-6000 per cm region at a resolution of 2.5 per cm using the moon as a source. An atmospheric modeling program and the AFGL line parameter atlas are used to identify H2O, CH4, O3 and other trace constituents and to derive stratospheric column densities (molecules/sq cm).

Smith, L. L.

Solar UV variability and its effect on stratospheric thermal structure and trace constituents

Observational evidence suggests the presence of solar UV variability in the spectral range 0.175-0.310 micron during the 11-year solar cycle. The present paper reports the results of a study using a steady-state 1-D radiative-convective-photochemical model conducted to determine the response of stratospheric temperatures and O3, O(1D), O(3P), and N2O constituent distributions to UV variability. Results show that concentrations of constituents and the thermal structure may be altered significantly for the altitude interval between 20 and 55 km.

Callis, L. B.

Inversion of stratospheric aerosol and gaseous constituents from spacecraft solar extinction data in the 0.38-1.0-micron wavelength region

The paper discusses a possible data retrieval technique for the spaceborne Stratospheric Aerosol and Gas Experiment (SAGE). The SAGE instrument has four radiometric channels located at selected intervals in the 0.38-1.0-micron wavelength range. A data reduction procedure is described for minimization of experimental errors on the basis of a detailed simulation of the measurement sequence. An efficient and accurate inversion method is then used for the retrieval of all the constituent vertical profiles. Also, the effects of horizontally inhomogeneous distributions of the constituent vertical profiles are studied based on available data of their global distributions. A simple horizontally inhomogeneous model of stratospheric aerosol and ozone is employed to estimate the perturbation on the retrieval accuracies.

Chu, W. P.

Stark cell optoacoustic detection of constituent gases in sample

An optoacoustic detector for gas analysis is implemented with Stark effect cell modulation for switching a beam in and out of coincidence with a spectral line of a constituent gas in order to eliminate the heating effect of laser energy in the cell as a source of background noise. By using a multiline laser, and linearly sweeping the DC bias voltage while exciting the cell with a multiline laser, it is possible to obtain a spectrum from which to determine the combinations of excited constituents and determine their concentrations in parts per million.

Margolis, J. S.

Laboratory measurements of microwave absorption from gaseous atmospheric constituents under conditions for the outer planets

Quite often the interpretive work on the microwave and millimeter-wave absorption profiles, which are inferred from radio occultation measurements or radio astronomical observations of the outer planets, employs theoretically-derived absorption coefficients to account for contributions to the observed opacity from gaseous constituents. Variations of the actual absorption coefficients from those which are theoretically derived, especially under the environmental conditions characteristic of the outer planets, can result in significant errors in the inferred abundances of the absorbing constituents. The recognition of the need to make laboratory measurements of the absorptivity of gases such as NH3, CH4, and H2O in a predominantly H2 atmosphere, under temperature and pressure conditions simulating the outer planets' atmospheres, and at wavelengths corresponding to both radio occultation and radio astronomical observations, has led to the development of a facility capable of making such measurements at Georgia Tech. The laboratory measurement system, the measurement techniques, and the proposed experimental regimen for Winter 1985 are described.

Steffes, Paul G.

Middle atmosphere trace constituents; Proceedings of Workshop 9 of the Twenty-sixth COSPAR Plenary Meeting, Toulouse, France, June 30-July 11, 1986

Papers are presented on a reference model for stratospheric NO2, a proposed reference model for nitric acid, proposed reference models for ozone, and a background stratospheric aerosol reference model. Other topics include a comparison between the observed and calculated distributions of trace species in the middle atmosphere, recent measurements of trace constituents from rocket and balloon probes, NO2 field observations in the stratosphere during the MAP/GLOBUS Campaign in 1983 and 1985, and the vertical distribution of ozone in the equatorial zone. Also considered are precision measurements of stratospheric ozone profiles by rocket-borne optical ozonesondes, vertical profiles of source gases at tropical latitudes, and measurements of stratospheric trace constituent distributions from balloon-borne far infrared observations.

Keating, G. M.

The evolution of AAOE observed constituents with the polar vortex

One of the difficulties in determining constituent trends from the ER-2 flight data is the large amount of day to day variability generated by the motion of the polar vortex. To reduce this variability, the observations have been transformed into the conservative (Lagrangian) reference frames consisting of the coordinate pairs, potential temperature (PT) and potential vorticity (PV), or PT and N2O. The requirement of only two independent coordinates rests on the assumption that constituent distributions and their chemical processes are nearly zonal in that coordinate system. Flight data is used everywhere for these transformation except for potential vorticity. Potential vorticity is determined from level flight segments, and NMC PV values during flight dives and takeoffs are combined with flight data in a smooth fashion.

Schoeberl, Mark R.

The use of assimilated stratospheric data in constituent transport calculations

A stratospheric assimilation system has been developed, which generates wind data that is consistent with the geopotential height (and temperature) field and the primitive equations in the general circulation model. This paper reports the first known calculations to use data from an assimilation to calculate constituent transport in the stratosphere. Nitric acid (NHO3) during the Limb IR Monitor of the Stratosphere (Gille et al., 1984) period is studied. The high-latitude time variance of the HNO3 is accurately captured. These studies suggest that data from an assimilation process offers tremendous potential for studying stratospheric dynamics, constituent transport, and chemistry.

Rood, Richard B.