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At least 73 records · Page 4

Guide for Oxygen Compatibility Assessments on Oxygen Components and Systems

A viewgraph presentation evaluating the compatibility of oxygen components and systems is shown. The topics include: 1) Application; 2) Gaining Wide Subscription; 3) Approach; 4) Establish Worst-Case Operating Conditions; 5) Assess Materials Flammability; 6) Evaluate Ignition Mechanisms; 7) Evaluate Kindling Chain; 8) Determine Reaction Affect; 9) Document Results; 10) Example of Documentation; and 11) Oxygen Compatibility Assessment Team.

Rosales, Keisa R.

Oxygen Isotopes in AMMS and IDPS: Universality of Oxygen Isotope Systematics Of Crystalline Silicates in Comets

It has been suggested that the major source of crystalline silicates in comets is CR chondrule-like materials along with minor sources including O, R, CH-CB chondrite chondrule-like materials based on the comparisons of oxygen isotope systematics between cometary silicates and chondrules from various types of primitive chondrites [1-3]. However, cometary silicates used for these studies are from only two comets: Wild2 and a parent comet of U2-20GCA. It is uncertain that the oxygen isotope systematics represent that of crystalline silicates in all comets.

D Nakashima

Activationof Oxygen Evolution Electrocatalysis viaReduced Ruthenium–Oxygen–Ruthenium Coordination

Noble metal oxides such as RuO2 are the state-of-the-art electrocatalysts for anodic reactions in acidic electrolytes, but their scarcity and moderate activity greatly limit emerging renewable energy technologies. Here, we show that oxidized overlayers of ruthenium on earth-abundant manganese oxide (MnO2/o-RuOx) nanocrystal supports exhibit Ru chemical states associated with reduced Ru–O–Ru coordination that enable dynamic switching of hydrogen bonding, with *OH intermediates hydrogen bonding to surface O and *OOH intermediates bonding to protruding RuOx clusters. The resulting electrocatalysts exhibit an overpotential of 218.9 ± 0.3 mV at 10 mA cm–2 for the oxygen evolution reaction in acid, corresponding to a 2425% increase in Ru mass activity compared to RuO2, enabling the construction of electrolyzers that achieved 3 A cm–2 at 1.646 V, 5.54 A cm–2 at 1.8 V, and exhibited over 3000-h stability at 100 mA cm–2. These findings motivate further efforts to develop nanomaterials that harness reduced Ru–O–Ru coordination to enable emerging renewable energy technologies.

58 GEOSCIENCES

The thermodynamic properties of oxygen and nitrogen. Part 2: Thermodynamic properties of oxygen from 100 R to 600 R with pressure to 5000 psia

An equation of state is presented for liquid and gaseous oxygen for temperatures from 100 R to 600 R and pressures to 5000 psia. The pressure-density-temperature data available from the published literature have been reviewed, and appropriate corrections have been applied to bring experimental temperatures into accord with the International Practical Temperature Scale of 1968. Representative comparisons of property values calculated from the equation of state to measured values are included to illustrate the accuracy of the equation of state. The coefficients of the equation of state were determined by a weighted least squares fit to selected published data, and simultaneously to isochoric heat capacity data, and to data which define the phase equilibrium for the saturated liquid and saturated vapor. The equation of state is estimated to be accurate for the liquid to within 0.1 percent in density, to within 0.2 percent for the vapor below the critical temperature and for states above the critical temperatures to 250 K, and within 0.1 percent for supercritical states at temperatures from 250 K to 300 K. The vapor pressure equation is accurate to within + or - 0.01 K between the triple point and the critical point.

Stewart, R. B.

ASRDI oxygen technology survey. Volume 5: Density and liquid level measurement instrumentation for the cryogenic fluids oxygen, hydrogen, and nitrogen

Information is presented on instrumentation for density measurement, liquid level measurement, quantity gauging, and phase measurement. Coverage of existing information directly concerned with oxygen was given primary emphasis. A description of the physical principle of measurement for each instrumentation type is included. The basic materials of construction are listed if available from the source document for each instrument discussed. Cleaning requirements, procedures, and verification techniques are included.

Roder, H. M.

Electrochemical oxygen concentrator as an oxygen compressor

A solid polymer electrolyte (SPE) oxygen compressor is described which generates pressures of 3000 psi. The SPE is a cation exchange membrane with chemical compatibility, and has the capability of withstanding 5000 psi. Other features of the compressor described include: gasketless sealing, porus plate cell supports, and conductive cooling. Results are presented of a computer program which defines the power of the system as a function of density, temperature, pressure, membrane thickness, and water content.

Source record

Detecting oxygen in hydrogen or hydrogen in oxygen

Catalytic sensor operates in high-pressure, moisture-laden gases. It was developed for life support system in which water is decomposed by electrolysis to produce oxygen and hydrogen. Sensor has potential applications in gas-detection and measurement instruments, particularly for gases generated by electrolysis, because such gases may contain large amounts of moisture.

Erickson, A. C.

Stellar oxygen abundances. 3: The oxygen abundance of the very metal poor halo star BD -13 deg 3442

A spectrum of the very metal poor ((Fe/H) approximately -3) halo star BD -13 deg 3442 is presented and used to determine this star's oxygen abundance. Our determination makes BD -13 deg 3442 the most metal poor dwarf (though a somewhat evolved one) with an O abundance determination. The O abundance (determined from the 7774 A O I triped) and (O/Fe) ratio is compared to that of two other metal-poor stars. The (O/Fe) ratio of BD -13 deg 3442 is found to be approximately 0.35 dex larger than that of the other two halo stars. Possible implications of this result are discussed.

King, Jeremy R.

Stellar oxygen abundances. 4: Systematic effects on oxygen abundances derived from the 6300 A (O I) and 7774 A O I lines

We consider potential systematic effects on oxygen abundances derived from the 6300 A (OI) line and the 7774 A OI triplet. Our solar intensity spectra of the 7774 A triplet confirm previous results which indicate a discrepancy between the observed equivalent widths of Altrock (1968) and the values predicted by Local Thermodynamic Equilibrium (LTE) and recent NLTE models. However, this disagreement (at low micron(s)) does not seem to affect the solar O abundance as derived from flux spectra. We derive O abundances for a selection of relatively metal-rich F and G dwarfs from both the 6300 A (OI) line and 7774 A OI triplet and detail the various uncertainties which enter into the analyses. Minimizing possible systematic effects to the extent possible, we find for T(sub eff) approximately less than 6200-6300 K no systematic difference between the 6300 and 7774 A abundances. For T(sub eff) approximately greater than 6200-6300 K, however 7774 A abundances are substantially larger than the 6300 A abundances. This agreement in O abundances from the two features at cooler T(sub eff) conflicts with that of others and we suggest that the discrepancy may be due to the different model atmospheres utilized. If recently proposed, hotter T(sub eff) values for metal-poor dwarfs are correct, then there appears to be no discrepancy between the 6300 A abundances of metal-poor giants are correct, then there appears to be no discrepancy between the 6300 A abundances of metal-poor giants or dwarfs and the 7774 A abundances for dwarfs. This would seem to rule out substantial LTE departures or atmospheric inhomogeneity effects skewing metal-poor O abundances from the 7774 A triplet (for cooler stars having low metallicity anyway). Given the repeated inability of authors to reproduce each others' O abundances from the 6300 A (OI) line and the uncertainties in the solar equivalent width, we question the usual assumption that the 6300 A (OI) line and the uncertainties in the solar equivalent width, we question the usual assumption that the 6300 A (OI) abundances are more reliable than those from the permitted triplet.

King, Jeremy R.

SPE (trademark) Oxygen Generator Assembly (OGA). (Refurbishment of the technology demonstrator LFSPE oxygen generation subsystem)

The SPE Oxygen Generator Assembly (OGA) has been modified to correct operational deficiencies present in the original system, and to effect changes to the system hardware and software such that its operating conditions are consistent with the latest configuration requirements for the International Space Station Alpha (ISSA). The effectiveness of these changes has recently been verified through a comprehensive test program which saw the SPE OGA operate for over 740 hours at various test conditions, including over 690 hours, or approximately 460 cycles, simulating the orbit of the space station. This report documents the changes made to the SPE OGA, presents and discusses the test results from the acceptance test program, and provides recommendations for additional development activities pertinent to evolution of the SPE OGA to a flight configuration. Copies of the test data from the acceptance test program are provided with this report on 3.5 inch diskettes in self-extracting archive files.

Roy, Robert J.

High-Precision Determination of Oxygen-Kalpha Transition Energy Excludes Incongruent Motion of Interstellar Oxygen

We demonstrate a widely applicable technique to absolutely calibrate the energy scale of x-ray spectra with experimentally well-known and accurately calculable transitions of highly charged ions, allowing us to measure the K-shell Rydberg spectrum of molecular O2 with 8 meV-uncertainty. We reveal a systematic ~450meV shift from previous literature values, and settle an extraordinary discrepancy between astrophysical and laboratory measurements of neutral atomic oxygen, the latter being calibrated against the aforementioned O2 literature values. Because of the widespread use of such, now deprecated, references, our method impacts on many branches of x-ray absorption spectroscopy. Moreover, it potentially reduces absolute uncertainties there to below the meV level.

M A Leutenegger