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At least 613 records · Page 34

Erosion Results of the MISSE 9-15 Polymers and Composites Experiment 1-4 (PCE 1-4)

Polymers and other oxidizable materials on the exterior of spacecraft in the low Earth orbit (LEO) space environment can be eroded from reaction with atomic oxygen (AO). Therefore, in order to design durable spacecraft it is important to know the extent of erosion that will occur during a mission. This can be determined by knowing the LEO AO erosion yield, E y (volume loss per incident oxygen atom), of materials susceptible to AO reaction. In addition, recent flight experiments have shown that the AO E y can vary with the AO fluence and/or solar exposure. Therefore, obtaining AO E y data for materials flown on various spaceflight missions is important. NASA Glenn Research Center has flown numerous experiments as part of the Materials International Space Station Experiment (MISSE) missions on the exterior of the International Space Station (ISS) to characterize the LEO E y of polymers, composites, protective coatings, and other spacecraft materials. Recently, four Glenn experiments with 365 flight (F) samples were flown on ISS’s MISSE-Flight Facility (MISSE-FF). These experiments are the Polymers and Composites Experiment-1 (PCE-1) flown as part of the MISSE-9 mission, the PCE-2 flown as part of the MISSE-10 mission, the PCE-3 flown as part of the MISSE-12 and MISSE-15 missions, and the PCE-4 flown as part of the MISSE-13 mission. Although each experiment had numerous sample objectives, the primary objective was to determine the LEO AO E y of various spacecraft materials as a function of solar irradiation and AO fluence. This paper provides a summary of the erosion data for the PCE 1-4 AO E y samples. The AO E y for 150 samples flown in either the LEO ram, wake, zenith or nadir directions are provided. The AO ram fluence varied from 2.97×10 20 atoms/cm 2 after 0.89 years of direct space exposure (with relatively high levels of Si contamination) on MISSE 12 to 3.93×10 20 atoms/cm 2 after 1.17 years of direct space exposure on MISSE-10. The ram AO E y values for uncoated polymers range from 3.81×10 –25 cm 3 /atom for polytetrafluoroethylene (M9R-C20 F) exposed to an AO fluence of 3.44×10 20 atoms/cm 2 on MISSE-9 to 4.43×10 –23 cm 3 /atom for AO etched low density polyimide aerogel (M12R-C21 F) exposed to an AO fluence of 2.97×10 21 atoms/cm 2 on MISSE-12. Because of the low AO fluence and relatively high Si contamination, a number of PCE-3 wake samples experienced mass gain. Thus, AO E y values are not provided for these samples. Although there are calculated AO E y values for the zenith, wake and nadir samples, the ram AO E y for a particular material is a more reliable value in terms of AO exposure because the zenith, wake and nadir directions were exposed to either no or very little AO fluence and thus other space environmental factors (i.e. vacuum, thermal extremes and thermal cycling, and/or various types of radiation) are responsible for the mass loss.

Erosion yield↗

Atomic oxygen-metal surface studies as applied to mass spectrometer measurements of upper planetary atmospheres

The problem of atomic oxygen loss in mass spectrometer ion sources can be reduced to an understanding of the possible surface interactions between oxygen atoms and the metal surface of the ion source. Results are presented for an experimental study in which an atomic oxygen beam apparatus and a mass spectrometer were used to measure the oxygen atom reflection, recombination, general surface reaction, and occlusion probabilities on six different engineering surfaces as a function of atomic oxygen exposure. The materials studied are gold, Nichrome V, aluminum, titanium, silver, and platinum. The variation in measured reflection probability seems to occur with metals that form oxides, Nichrome V being stable in terms of reflection stability. Recombination is observed an all surfaces except aluminum and platinum. Variation in the complete set of measurements in a single experiment is the result of varying surface conditions.

Sjolander, G. W.↗

Catalytic processes in the atmospheres of earth and Venus

Photochemical processes in planetary atmospheres are strongly influenced by catalytic effects of minor constituents. Catalytic cycles in the atmospheres of Earth and Venus are closely related. For example, chlorine oxides (ClOx) act as catalysts in the two atmospheres. On earth, they serve to convert odd oxygen (atomic oxygen and ozone) to molecular oxygen. On Venus they have a similar effect, but in addition they accelerate the reactions of atomic and molecular oxygen with carbon monoxide. The latter process occurs by a unique combination of ClOx catalysis and sulful dioxide photosensitization. The mechanism provides an explanation for the very low extent of carbon dioxide decomposition by sunlight in the Venus atmosphere.

Demore, W. B.↗

Thermochemical analyses of the oxidative vaporization of metals and oxides by oxygen molecules and atoms

Equilibrium thermochemical analyses are employed to describe the vaporization processes of metals and metal oxides upon exposure to molecular and atomic oxygen. Specific analytic results for the chromium-, platinum-, aluminum-, and silicon-oxygen systems are presented. Maximum rates of oxidative vaporization predicted from the thermochemical considerations are compared with experimental results for chromium and platinum. The oxidative vaporization rates of chromium and platinum are considerably enhanced by oxygen atoms.

Kohl, F. J.↗

Ozone Depletion, UVB and Atmospheric Chemistry

The primary constituents of the Earth's atmosphere are molecular nitrogen and molecular oxygen. Ozone is created when ultraviolet light from the sun photodissociates molecular oxygen into two oxygen atoms. The oxygen atoms undergo many collisions but eventually combine with a molecular oxygen to form ozone (O3). The ozone molecules absorb ultraviolet solar radiation, primarily in the wavelength region between 200 and 300 nanometers, resulting in the dissociation of ozone back into atomic oxygen and molecular oxygen. The oxygen atom reattaches to an O2 molecule, reforming ozone which can then absorb another ultraviolet photon. This sequence goes back and forth between atomic oxygen and ozone, each time absorbing a uv photon, until the oxygen atom collides with and ozone molecule to reform two oxygen molecules.

Stolarski, Richard S.↗

Ozone Depletion, UVB and Atmospheric Chemistry

The primary constituents of the Earth's atmosphere are molecular nitrogen and molecular oxygen. Ozone is created when ultraviolet light from the sun photodissociates molecular oxygen into two oxygen atoms. The oxygen atoms undergo many collisions but eventually combine with a molecular oxygen to form ozone (O3). The ozone molecules absorb ultraviolet solar radiation, primarily in the wavelength region between 200 and 300 nanometers, resulting in the dissociation of ozone back into atomic oxygen and molecular oxygen. The oxygen atom reattaches to an O2 molecule, reforming ozone which can then absorb another ultraviolet photon. This sequence goes back and forth between atomic oxygen and ozone, each time absorbing a uv photon, until the oxygen atom collides with and ozone molecule to reform two oxygen molecules.

Stolarski, Richard S.↗

Follow-up on the effects of the space environment on UHCRE thermal blankets

An overview of the effects of the space environment on the thermal blanket of the UHCRE experiment is presented with an emphasis on atomic oxygen (AO) erosion. A more accurate value for FEP Teflon reaction efficiency is given and corresponds, at normal incidence, to 3.24 10(exp -25) cu cm/atomic, therefore, the FEP Teflon erosion corresponding to the Long Duration Exposure Facility (LDEF) total mission is 29.5 microns. A power 1.44 of the cosine of the incident angle of the oxygen atoms is found. It is shown that this value is not far from the power found using Fergusson's relationship between efficiency and energy of the O-atoms. An hypothesis concerning the effect of oxygen ions (O(+)) is also presented. The presence of oxygen ions may explain the different results obtained from different flights and from laboratory tests. Finally an XPS analysis of Chemglaze Z306(tm) black paint demonstrates the presence of silicone in the paint which may explain part of the contamination found on LDEF.

Levadou, Francois↗

An overview of the first results on the solar array materials passive LDEF experiment (sample), A0171

Power degradation in the solar cells was consistent with the exposure environment and appears to be produced principally by the radiation and atomic oxygen environments. Atomic oxygen erosion was generally as expected; atomic oxygen effects dominated for the most part in materials that were both atomic oxygen and ultraviolet vulnerable. Silicone coatings appear to protect Kapton, and adhesive systems contained under photon opaque materials were surprisingly environmentally resistant. A high density of small micro-meteroid/space debris impacts were observed on mirrors, protective coatings, paints, and composites. New synergistic effects of the space environment were noted in the interaction of atomic oxygen and copious amounts of contamination and in the induced luminescence of many materials.

Ann F Whitaker↗

The dissociation of OH and OD in comets by solar radiation

Calculations of the radiative lifetimes of cometary OH are presented as a function of the radial velocity of the comet and of the velocity distributions of the hydrogen and oxygen atoms produced by photodissociation of OH. The contribution of the photodissociation of OH to the emission of the red and green lines of atomic oxygen is assessed. An estimate is made of the lifetime of OD and of the velocity distribution of the deuterium atoms.

Van Dishoeck, E. F.↗

Complexity in the Photofunctionalization of Single-Wall Carbon Nanotubes with Hypochlorite

The reaction of aqueous suspensions of single-wall carbon nanotubes (SWCNTs) with UV-excited sodium hypochlorite has previously been reported to be an efficient route for doping nanotubes with oxygen atoms. Here, we have investigated how this reaction system is affected by pH level, dissolved O 2 content, and radical scavengers and traps. Products were characterized with near-IR fluorescence, Raman, and XPS spectroscopy. The reaction is greatly accelerated by removal of dissolved O 2 and strongly suppressed by TEMPO, a radical trap. Alcohols added as radical scavengers alter the reaction efficiency and the product peak emission wavelengths. Photofunctionalization with 300 nm irradiation is substantially less efficient at pH levels low enough to protonate the OCl – ion to HOCl. We deduce that in mildly treated high pH samples, the main product is sp 2 hybridized O-doped adducts formed by reaction of SWCNTs with atomic oxygen in its 3 P (ground) level. By contrast, treatment under low pH conditions leads to sp 3 hybridized SWCNT adducts formed by the addition of secondary radicals from reactions of • OH and • Cl. There is also evidence for additional photoreactions of product species under stronger irradiation. Researchers using photoexcited hypochlorite for SWCNT functionalization should be alert to the range of products and the sensitivity to reaction conditions in this system.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Solar-wind interactions - Nature and composition of lunar atmosphere

The nature and composition of the lunar atmosphere are examined on the basis of solar-wind interactions, and the nature of the species in the trapped-gas layer is discussed using results of theoretical and experimental investigations. It is shown that the moon has a highly tenuous atmosphere consisting of various species derived from five sources: solar-wind interaction products, cosmic-ray interaction products, effects of meteoritic impacts, planetary degassing, and radioactive-decay products. Atmospheric concentrations are determined for those species derived from solar-wind protons, alpha particles, and oxygen ions. Carbon chemistry is briefly discussed, and difficulties encountered in attempts to determine quantitatively the concentrations of molecular oxygen, atomic oxygen, carbon monoxide, carbon dioxide, and methane are noted. The calculated concentrations are shown to be in good agreement with observations by the Apollo 17 lunar-surface mass spectrometer and orbital UV spectrometer.

Mukherjee, N. R.↗

Absorption cross sections of some atmospheric molecules for resonantly scattered O I 1304-A radiation

Absorption cross sections for O2, N2, CO2, CH4, N2O, and CO have been measured at each of the lines of the atomic oxygen triplet at 1302, 1305, and 1306 A. Radiation resonantly scattered from oxygen atoms at a temperature of about 300 K was used for the line source. Absorber temperatures were also near 300 K. Direct application of the Lambert-Beer absorption equation yielded pressure-dependent cross sections for carbon monoxide at each line of the O I triplet. Reasons for this apparent dependence are presented and discussed.

Starr, W. L.↗

Structure of the neutral upper atmosphere of Mars - Results from Viking 1 and Viking 2

Neutral mass spectrometers carried on the aeroshells of Viking 1 and Viking 2 indicate that carbon dioxide is the major constituent of the Martian atmosphere over the height range 120 to 200 kilometers. The atmosphere contains detectable concentrations of nitrogen, argon, carbon monoxide, molecular oxygen, atomic oxygen, and nitric oxide. The upper atmosphere exhibits a complex and variable thermal structure and is well mixed to heights in excess of 120 kilometers.

Nier, A. O.↗

Nitric oxide delta band emission in the earth's atmosphere - Comparison of a measurement and a theory

Attention is given to the altitude dependent emission rate in the delta-bands of nitric oxide as measured in the earth's atmosphere at night by a scanning ultraviolet spectrometer. It is noted that the reaction responsible is the two-body association of nitrogen and oxygen atoms. The measurements show a vertical intensity beneath the layer for the delta-band system of 19 R. The horizontal emission rate is found to increase from 70 R at 117 km to 140 R at 150 km. The data are analyzed with a one-dimensional, time-dependent, vertical-transport model of odd nitrogen photochemistry. The calculated and measured intensities agree so long as the quenching of N(2D) by atomic oxygen is near 5 x 10 to the -13 cu cm/sec.

Rusch, D. W.↗

Sputtered coatings for protection of spacecraft polymers

Kapton polyimide oxidizes at significant rates (4.3x10(-24) gram/incident oxygen atom) when exposed in low Earth orbit to the ram atomic oxygen flux. Ion beam sputter deposited thin films of Al2O3 and SiO2 as well as a codeposited mixture of predominantly SiO2 with a small amount of polytetrafluoroethylene were evaluated and found to be effective in protecting Kapton from oxidation in both laboratory plasma ashing tests as well as in space on board shuttle flight STS-8. A protective film of or = 96 percent SiO2 and or = 4 percent polytetrafluoroethylene was found to be very flexible compared to the pure metal oxide coatings and resulted in mass loss rates that were 0.2 percent of that of the unprotected Kapton. The optical properties of Kapton for wavelengths investigated between 0.33 and 2.2 microns were not significantly altered by the presence of the coatings or changed by exposure of the coated Kapton to the low Earth orbital ram environment.

Banks, B. A.↗

The production of glow precursors by oxidative erosion of spacecraft surfaces

Erosion rates of organic materials are measured during a recent flight of the shuttle (STS-8). Several forms of carbon and a variety of thermosetting and thermoplastic polymers are exposed to the ram beam of atomic oxygen. Arrhenius energies of about 1000 to 2000 cal/mole were measured from the rate dependencies on temperature. If some simple assumptions are made about the chemical nature of the desorbed species, the data can be used to estimate production rates at surfaces in orbit under different conditions of temperature, oxygen atom flux, and material surface conditions.

Gregory, J. C.↗

Degradation studies of SMRM Teflon

A working group was organized to study materials and components of the Solar Max Satellite (SMS) that was returned by the STS 41C. These materials were exposed in space for 50 months and represent the only real time long term exposure data available to date. In the molecular modeling of material and energetic oxygen atom interaction, it is pointed out that the importance of developing correlation between accelerated exposure data from STS and some real time data. In particular, it was predicted that Teflon which showed no detectable degradation on various STS flights may be susceptible to atomic oxygen degradation under real time conditions. Initial inspection of returned SMS samples showed that Teflon suffered visual damage such as cracking and yellowing. The results of examination of these samples are given.

Liang, R. H.↗