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At least 325 records · Page 18

Further developments in oxidation of methane traces with radiofrequency discharge

The radiofrequency discharge, previously shown to oxidize trace levels of methane in oxygen, was studied with contaminated air at 50, 600, and 760 torr. As with oxygen, the concentration of methane traces could be reduced by several orders of magnitude, and no organic reaction products were detected in the effluent; however, substantial concentrations of NOx (0.1-6%) were formed during treatment. The concentration of NOx was decreased by using a large diameter electrode. There is evidence that the process will oxidize N2 and NO as well as organic impurities in oxygen or oxygen/inert gas atmospheres.

Flamm, D. L.↗

The capability of satellite borne remote sensors to measure stratospheric trace constituents. Volume 3: Supporting material

Contained in this volume is material of a supportive nature not considered to be of sufficient importance to be included in the other two previous volumes. This material is of two types:(1) information and numerical evaluations used in the development of mission evaluations for stratospheric trace constituent measurement;and (2) various spatial and temporal distributions for those stratospheric trace species having sufficient measurements available to warrant their presentation.

Keitz, E. L.↗

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.↗

Trace element contents of selected antarctic meteorites, 1

Data are reported for volatile/mobile Ag, As, Au, Bi, Cd, Co, Cs, Cu, Ga, In, Rb, Sb, Se, Te, T1 and Zn in exterior and/or interior samples of four Antarctic meteorites: 77005 (unique achondrite); 77257 (unreilite); 77278 (L3); 77299 (H3). Exterior samples reflect contamination and/or leaching by weathering but trace element (ppm-ppt) contents in interior samples seem reasonable for representatives of these rare meteoritic types. The 77005 achondrite seems related to shergottites; other samples extend compositional ranges previously known for their types. With suitable precautions, Antarctic meteorite finds yield trace element data as reliable as those obtained from previously known falls.

Biswas, S.↗

Trace constituent mixing ratios in the lower stratosphere during the 1977 intertropical convergence zone experiment

Minor constituents in the atmosphere can play an important role as tracers in studies of atmospheric transport and mixing. Simultaneous measurements of the vertical distribution of trace constituents in the troposphere and lower stratosphere were conducted in the region of the Intertropical Convergence Zone (ITCZ). An effort was made to measure the mixing ratios of selected trace constituents. A cryogenic sampling system on board a U-2 aircraft was used to acquire whole-air samples and to cryogenically collect samples at 13.7 to 21.3 km. Simultaneous tropospheric measurements using whole-air sampling canisters on board a Learjet aircraft were also carried out.

Vedder, J. F.↗

Trace element partitioning between ionic crystal and liquid

The partitioning of trace elements between ionic crystals and the melt has been correlated with lattice energy of the host. The solid-liquid partition coefficient has been expressed in terms of the difference in relative ionic radius of the trace element and the homogeneous and heterogeneous strain of the host lattice. Predictions based on this model appear to be in general agreement with data for alkali nitrates and for rare-earth elements in natural garnet phenocrysts.

Tsang, T.↗

Trace element composition of Luna 24 Crisium VLT basalt

The origins of the individual particles analyzed from the Luna 24 core and the information they provide on the trace-element composition of Mare Crisium basalt are considered. Previous analyses of several Luna 24 soil fragments are reviewed. It is concluded that: (1) the average trace-element concentrations for 12 VLT basalt fragments are the best available estimates for bulk samples of Crisium VLT basalt; (2) there is weak evidence that the average Crisium basalt might have a small positive Eu anomaly relative to chondritic matter; (3) the soils contain components from sources other than the Crisium VLT basalt; and (4) there is no convincing information in concentrations of rare-earth elements, Co, Sc, FeO, or Na2O among the analyzed fragments to indicate more than one parent basalt.

Haskin, L. A.↗

Genesis of Apollo 15 olivine normative mare basalts - Trace element correlations

Chemical and petrographic studies of 21 Apollo 15 rake basalts are reported; one pyroxene-phyric basalt, four olivine-phyric basalts, 15 olivine microgabbros, and one brecciated basalt are distinguished. The olivine-normative basalts (i.e., all samples but the pyroxene-phyric basalt) show correlation trends of La/Sm vs. La and Sm/Eu vs. La that are within the observed dispersion ranges of La/Sm and Sm/Eu ratios for a single lava flow. Trace element fractionation trends in the sample could be due to mobilization (perhaps by filter pressing) of fractionated residual liquid during the crystallization of a lava flow. However, it is also possible that the suite of olivine-normative basalts represents several basalt flows produced by partial melting of cumulate layers having interstitial liquids with variable trace-element compositions.

Ma, M.-S.↗

Experimental investigations of trace element fractionation in iron meteorites. I - Early results

Experimental procedures for measuring trace element partitioning among metal and sulfide and silicate phases are described, and solid metal/liquid metal partition coefficients for minor and trace elements in the Fe-Ni system at 5 to 14% Ni are reported. The bulk compositions desired are homogenized at superliquidus temperature for 15-24 hours, held at a temperature in the solid/liquid two phase region for about 24 hours, and quenched to freeze in the equilibrium compositions. Run products are analyzed by electron microprobe. With the exception of Cr, all preliminary partition coefficients obtained are in the same sense as values derived from iron meteorites. The partition coefficients for Cr in solid metal/liquid metal and metal/troilite systems suggest that IIIAB and main group pallasites equilibrated with 9-22% troilite. A second method which makes it possible to place upper and lower limits on the partition coefficient by holding part of the sample at subliquidus and part at superliquidus temperatures, yielded significantly different results for the two metals tested (Au and Pt) from those obtained by the first method, demonstrating the importance of a close approach to equilibrium before using experimentally-determined partition coefficients to test empirical differentiation models for iron meteorites.

Bild, R. W.↗

Design and development of a trace contaminant removal canister for Spacelab

The paper describes the overall approach used by NASA-MSFC to design and develop a trace contaminant removal canister for Spacelab. The elements of this approach include the establishment of a trace contaminant load model, analysis and testing to define a preliminary design, development testing to verify the adequacy of the selected design, and testing to define a suitable canister location in the transfer tunnel ventilation system. The canister utilizes a catalyst material which is effective in removing carbon monoxide at room temperature, as well as plain and acid treated charcoal. The canister alone will control all contaminants in the load model below their maximum allowable concentration (MAC) levels without assistance from the baseline environmental control system (ECS) except for methyl alcohol and ammonia.

Ray, C. D.↗

Trace element contents of selected Antarctic meteorites. I - Weathering effects and ALH A77005, A77257, A77278 and A 77299

Data is examined for volatile/mobile Ag, As, Au, Bi, Cd, Co, Cs, Cu, Ga, In, Rb, Sb, Se, Te, Tl and Zn in exterior and/or interior samples of four Antarctic meteorites from the Allan Hills (ALH): A77005 (unique achondrite); A77257 (ureilite); A77278 (L3); A77299 (H3). Exterior samples reflect contamination and/or leaching by weathering but trace element (ppm-ppt) contents in interior samples seem reasonable for representatives of these rare meteoritic types. The A77005 achondrite is shown to be related to shergottites; other samples extend compositional ranges previously known for their groups or types. With suitable precautions, Antarctic meteorite finds yield trace element data as reliable as those obtained from previously known falls.

Biswas, S.↗

Trace elements in ocean ridge basalt glasses - Implications for fractionations during mantle evolution and petrogenesis

Seven documented and fresh glassy selvages from ocean floor basalt pillows were analyzed for trace elements including Ag, Au, Bi, Br, Ni, Pd, and Zn using radiochemical activation analysis. Glasses from DSDP leg 24, site 238 in the Indian Ocean have a trace element pattern which reflects secondary processes at a shallow depth. Chemical fractionations in petrogenesis of tholeiitic basalts indicate that (Ir, Os), Au, Pd, Ni, and Re are strongly fractionated in igneous processes; the unfractionated chondritic mantle pattern thus imposes constraints on mantle evolution models. Finally, the limited Rb/Cs fractionation in oceanic tholeiites reflects the low abundance of volatiles and hydrous silicates in normal ocean ridge basalts.

Hertogen, J.↗

Atmospheric trace gases - Possibility of sources in the Southern Hemisphere

When measurements of globally distributed trace gases establish their existence in the Southern Hemisphere, it is not always clear whether their presence is due to transport from the Northern Hemisphere or partly from significant sources in the Southern Hemisphere. In this paper a simple criterion is developed whereby one can determine if significant Southern Hemisphere sources exist for a given trace gas. Despite the limitations of the model, there are strong indications that C2 hydrocarbons (C2H2, C2H4, C2H6), CO and CH4 have significant Southern Hemisphere sources.

Khalil, M. A. K.↗

Greenhouse effect of trace gases, 1970-1980

Increased abundances were measured for several trace atmospheric gases in the decade 1970-1980. The equilibrium greenhouse warming for the measured increments of CH4, chlorofluorocarbons and N2O is between 50% and 100% of the equilibrium warming for the measured increase of atmospheric CO2 during the same 10 years. The combined warming of CO2 and trace gases should exceed natural global temperature variability in the 1980's and cause the global mean temperature to rise above the maximum of the late 1930's.

Lacis, A.↗

An advective model for two-dimensional transport of stratospheric trace species

A parameterization of two-dimensional transport is applied to photochemical models of stratospheric trace species. It is shown that in a first approximation, tracer transport in the meridional plane may be treated as an advective rather than a diffusive process. The concept of residual mean meridional circulation (Andrews and McIntyre, 1976; Boyd, 1976) is used in the model and shown to be a modified Eulerian mean, a good approximation to the Lagrangian mean motion. A simple example in which the equilibrium distribution is computed for a tracer with a uniform tropospheric source and a stratospheric sink proportional to the local mixing ratio demonstrates the potential of the proposed parameterization. The resulting distribution is found to agree qualitatively with the observed stratospheric distribution of trace species whose sources are in the troposphere.

Holton, J. R.↗

Solar UV variability - Effects on stratospheric ozone, trace constituents and thermal structure

The effect of long-term (11-year solar cycle) solar UV variability on stratospheric chemical and thermal structure has been studied using a time-dependent one-dimensional model. Previous studies have suggested substantial variations in local and total ozone, and in stratospheric thermal structure from solar minimum to solar maximum. It is shown that significant variations also occur in some of the trace constituents. Members of the HOx family and N2O exhibit the largest variations, and these changes, if detected, may provide additional means of verifying the presence of solar UV variability and its effects. Some of the species show large phase differences with the assumed solar flux variation. The role of chemical and transport time constants on the time variations of the trace species is examined. Comparisons with reported ozone and temperature data show reasonable agreement for the period 1960 to 1972.

Natarajan, M.↗

Natural and anthropogenic trace gases in the southern hemisphere

The complexity of the global environment makes it necessary that many important trace gases in the earth's atmosphere be measured on a global scale before predictions can be made regarding the effects of human activities on the environment. A description is presented of measurements of 14 atmospheric trace gases in the lower atmosphere (0-4 km) of the southern hemisphere. Concentrations are considered of CCl3F, CCl2F2, CHClF2, C2.Cl3.F3, CH3CCl3, CCl4, C2.Cl4, CH3I, CHCl3, CO, CH3Cl, CH4, N2O, and OCS. The obtained data are analyzed and interpreted to statistically quantify the possible differences of concentrations in and above the boundary layer, to model the vertical profile of CH3I, and to use the data in support of previous findings that CH4 is increasing in the atmosphere.

Rasmussen, R. A.↗

Application of ion-induced nucleation mass spectrometry in the analysis of trace gases evolved from a polyimide film during the thermal curing stages

Trace gases evolved from a polyimide film during its thermal curing stages have been studied using ion-induced nucleation mass spectrometry. The technique involved exposing the test gas sample to a low energy beta source and recording the masses of the ion-induced molecular clusters formed in the reaction chamber. On the basis of the experimentally observed molecular cluster spectra, it has been concluded that the dominant trace component had a molecular weight of 87 atomic mass units. This component has been identified as a molecule of dimethylacetamide (DMAC) which had been used as a solvent in the preparation of the test polyimide specimen. This identification has been further confirmed by comparing the spectra of the test gas sample and the DMAC calibration sample obtained with a conventional mass spectrometer. The advantages of the ion-induced nucleation mass spectrometer versus the conventional mass spectrometer are discussed.

Smith, A. C.↗