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At least 127 records · Page 7

Monitoring of impurities in fluids and gases

Aerospace requirements have engendered the need for instruments for automatic determination of trace impurities in liquid and gaseous systems by in-line continuous operation. These include devices for the automatic sizing and counting of minute particles (below 0.1 mm) is closed liquid and gaseous systems, and the automatic determination of nonvolatile residue in solvents and traces of hydrocarbons dissolved or dispersed in gaseous systems. The principle of operation, and characteristics of instruments, as well as results of experimental testing, are briefly described. Potential industrial applications are also suggested.

Impurity↗

Apparatus automatically measures soluble residue content of volatile solvents

Solvent Purity Meter /SPM/ automatically measures the soluble residue in volatile solvents used in cleaning or extraction of oils, greases, and other nonvolatile materials. The SPM gives instantaneous and continuous readout of soluble contaminant residues in concentrations as low as one part per million of solution.

Oswalt, F. W.↗

Read-only Memories Final Report

Integrated, metal oxide semiconductor memories with nonvolatile and electrically programmable characteristics

Cricchi, J. R.↗

Research on variable threshold transistor storage systems

A fully integrated, electrically alterable, nonvolatile, nondestructive readout control memory was developed, using as storage elements metal-nitride-silicon variable threshold transistors. An optimum approach to such a memory was developed in which a three dimensional selection technique was used, both for read and write operations. Electrical isolation of writing and memory circuits was obtained by means of separate memory and write circuit chips. This method provided protection from voltage breakdowns, increased circuit flexibility, and greater ease of testing of interim and final circuit elements.

Wegener, H. A. R.↗

Elemental abundances in stone meteorites.

Measurement of abundances of Na, Al, Sc, Cr, Mn, Fe, Co, and Cu by instrumental neutron activation analyses of 103 chondrites and 17 achondrites. Various sources of error in the method, including sampling errors, are discussed in detail. Examination of the patterns of coherence of the elements determined suggests the presence of effects of fractionation during condensation from the solar nebula of matter parental to chondrites. Such effects seem to be exhibited both in the abundances of lithophilic elements, perhaps being related to varied temperatures of accretion and in the abundances of those elements which would be affected by metal-silicate fractionation in the solar nebula. Atomic abundances relative to Si vary little in carbonaceous chondrites, suggesting that efficient mixing processes operated on these meteorites prior to or during their formation. It is suggested that, at present, no single class of carbonaceous chondrites is clearly more primitive than another. Carbonaceous and unequilibrated ordinary chondrites may represent aggregates of material accreted from the solar nebula at relatively low temperatures. The present data support a model of equilibration and minor mobilization of nonvolatile elements within small domains of chondrites after accretion. Such a model would be consistent with the petrologic types of Van Schmus and Wood (1967).

Schmitt, R. A.↗

Gas-liquid chromatography in lunar organic analysis.

Gas-liquid chromatography (GLC) is a powerful and sensitive method for the separation and detection of organic compounds at nanogram levels. The primary requirement for successful analyses is that the compounds of interest must be volatile under the chromatographic conditions employed. Nonvolatile organic compounds must be converted to volatile derivatives prior to analysis. The derivatives of choice must be both amenable to chromatographic separation and be relatively stable. The condition of volatility necessitates the development of efficient derivatization reactions for important groups of compounds as amino acids, carbohydrates, nucleosides, etc. Trimethylsilylation and trifluoroacetylation represent specific areas of recent prominence. Some relevant practical aspects of GLC are discussed.

Gehrke, C. W.↗

Chemical and petrographic correlations among carbonaceous chondrites

Detailed study of the petrographic and chemical properties of carbonaceous chondrites shows that the four distinct petrographic subtypes may be related to one of two distinct chemical subdivisions. These subdivisions are recognized primarily by the relative abundances of the nonvolatile elements Si, Ca, Al, Ti, Cu and Fe. C1, C2 and C3(O) chondrites form one subdivision. Vigarano subtype chondrites form the other subdivision and include chondrites previously referred to as C2, C3 and C4. Normalized to silicon, the abundances of Ca, Al and Ti are relatively enriched in Vigarano subtype chondrites, whereas Fe and Cu are relatively more abundant in C1, C2 and C3(O) chondrites. Volatile elements tend to correlate with petrographic subtypes rather than with chemical subdivisions.

Van Schmus, W. R.↗

Labile and nonlabile element relationships among Apollo 17 samples

Volatile and nonvolatile trace element contents in a suite of Apollo 17 soils and rocks are studied. It is found that the halogens exhibit a remarkable degree of coherence because of their apparent diverse geochemistry, that the F-Cl-P2O5 coherence previously noted persists among Apollo 17 samples, that both U and Ru-Os support lateral mixing of regolith on a local scale, and that the meteoritic Ru/Os ratios found in a few samples are attributed to primitive lunar material that has not been extensively recycled.

Jovanovic, S.↗

Mariner mission to Encke 1980

Experimental design for the Mariner mission to Comet Encke is considered, examining the following experiments: volatile and nonvolatile chemical analysis, an imaging system for the comet nucleus, the ultraviolet spectrometer, and magnetic field and plasma experiments. Mission design is discussed, emphasizing the mission profile, trajectory and targeting and the spacecraft design.

Yeates, C. M.↗

Volatile element depletion and K-39/K-41 fractionation in lunar soils

Evidence for selective loss and isotopic fractionation (in the case of K) of volatile elements during formation of agglutinates by micrometeoritic bombardment of lunar soils is presented. Concentrations and isotopic compositions of volatile elements (K, Rb, Pb) and nonvolatile elements (U, Th, Ba, Sr, rare earths) in separates taken from soils 14163, 14259, 15041, 68501, and 71500 are examined. Rayleigh fractionation calculations applied to K-39/K-41 isotopic data indicate ten-fold recycling of bulk soil, to account for observed isotopic anomalies. The lunar soil fines fraction seems to be a site of deposition for volatile or labile Pb produced during agglutination. Local fines (below 75 microns) are viewed as representative of the parent material for agglutinates formed in situ by micrometeoritic impact. Magnetic separation of agglutinates from soil 68501 revealed a bimodal population, with one class comprising welded blocky magnetic glasses.

Church, S. E.↗

Low-work-function surfaces produced by cesium carbonate decomposition

Cesium carbonate (Cs2CO3) was heated to the decomposition temperature of approximately 600 C. The nonvolatile decomposition products were condensed on a nickel substrate while the carbon dioxide was removed by pumping. The deposited material is characterized by an effective work function of between 1.05 and 1.15 eV at 450 K and by photoemission in the visible and near-infrared region of the spectrum. It is suggested that the deposited material consists of Cs2O, possibly Cs2O2, and adsorbed cesium. Silver, evaporated from a heated silver bead, produced the typical photoemissive and thermionic properties of a silver-oxygen-cesium (S-1) photocathode. The material may be of interest for thermionic energy converters and for the formation of silver-oxygen-cesium photocathodes.

Briere, T. R.↗

Volatile/mobile trace elements in Karoonda /C4/ chondrite

Concentrations of ten volatile/mobile trace elements and of nonvolatile Co in the Karoonda (C4) meteorite were determined, and the atomic abundances relative to C1 are compared with values for the Murchison (C2) and Allende (C3) meteorites. Empirical Bi, In, and Tl data for Karoonda and heated Allende and Murchison are compared with theoretical curves for condensation from a gas of cosmic composition at low pressures. It is suggested that Karoonda might derive from low-temperature open-system metamorphism of pristine C3-like material.

Matza, S. D.↗

Meteor ablation spheres from deep-sea sediments

Spheres from mid-Pacific abyssal clays (0 to 500,000 yrs old), formed from particles that completely melted and subsequently recrystallized as they separated from their meteoroid bodies, or containing relict grains of parent meteoroids that did not experience any melting were analyzed. The spheres were readily divided into three groups using their dominant mineralogy. The Fe-rich spheres were produced during ablation of Fe and metal-rich silicate meteoroids. The glassy spheres are considerably more Fe-rich than the silicate spheres. They consist of magnetite and an Fe glass which is relatively low in Si. Bulk compositions and relict grains are useful for determining the parent meteoroid types for the silicate spheres. Bulk analyses of recrystallized spheres show that nonvolatile elemental abundances are similar to chondrite abundances. Analysis of relict grains identified high temperature minerals associated with a fine-grained, low temperature, volatile-rich matrix. The obvious candidates for parent meteoroids of this type of silicate sphere is a carbonaceous chondrite.

Blanchard, M. B.↗

Trace elements in ocean ridge basalts

A study is made of the trace elements found in ocean ridge basalts. General assumptions regarding melting behavior, trace element fractionation, and alteration effects are presented. Data on the trace elements are grouped according to refractory lithophile elements, refractory siderophile elements, and volatile metals. Variations in ocean ridge basalt chemistry are noted both for regional and temporal characteristics. Ocean ridge basalts are compared to other terrestrial basalts, such as those having La/Yb ratios greater than those of chondrites, and those having La/Yb ratios less than those of chondrites. It is found that (1) as compared to solar or chondrite ratios, ocean ridge basalts have low ratios of large, highly-charged elements to smaller less highly-charged elements, (2) ocean ridge basalts exhibit low ratios of volatile to nonvolatile elements, and (3) the transition metals Cr through Zn in ocean ridge basalts are not fractionated more than a factor of 2 or 3 from the chondritic abundance ratios.

Kay, R. W.↗

Monochromatic brightness variations of comets. II - Core-mantle model

A class of comets, of which Comet Kohoutek (1973f) is typical, show total as well as monochromatic brightness asymmetries about perihelion. They are fainter after perihelion than before at the same heliocentric distance. A model of the cometary nucleus consisting of a growing nonvolatile dust mantle surrounding a volatile icy core is used to discuss this phenomenon. Numerical results are obtained for Comet Kohoutek (1973f). It is found that dust mantles of thickness in the range of 10-75 cm can be grown by perihelion passage for various values of the thermal conductivity of the dust if there is no substantial dust blow-off by the sublimating volatiles. The thermal conductivity of the dust mantle is quite small and is dominated by 'radiative conductivity' for heliocentric distances less than about 2 AU. Since the radiative conductivity is larger for larger grain size, the thickest mantle corresponds to coarsest matrix. The production rate of the 'parent-molecules' as well as the monochromatic brightness of their 'daughter' products increases less steeply than in the mantleless case, as the comet approaches perihelion.

Mendis, D. A.↗

Ancient meteoritic component in Apollo 17 boulders

The reported investigation is concerned with the resolution of a number of questions related to the ancient meteoritic component in Apollo 17 boulders. Numerical taxonomic methods have been adopted to objectively group the components. Only the nonvolatile siderophile elements have been used for the classification. Efforts were made to obtain data on the metal composition of breccias analyzed for trace elements, to determine if metal homogeneity was reflected in siderophile ratios. Thirty-one samples were analyzed of which twenty-eight have significant siderophile contents. It is concluded that highland breccias are largely the product of large basin-forming impacts. Highland soils are then produced by comminution of the breccias by small local impacts and micrometeorite bombardment. The long-lived component of bulk soils considered by Baedecker et al. (1974) is thought to contain a substantial micrometeorite contribution, plus assorted debris.

Higuchi, H.↗