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At least 1,027 records · Page 57

Radioactivities in returned lunar materials

Results from a carbon-14 study in size fractions of lunar soil are reported. The 10 to 30 micrometers and 74 to 124 micrometers size fraction results were supplemented by 30 to 37 micrometers results that are given in this report. The gases from the less than 10 micrometers fraction were extracted and purified and carbon-14 counting is now in progress. Meteorites were also studied using carbon-14, with emphasis directed to those recently discovered in the Antarctic.

Fireman, E. L.↗

Trace element geochemistry and the early lunar differentiation

The results are considered of experiments in which thermal neutron activation analysis was used to measure the halogens, U, Te, Ru, Os, and Hg in lunar samples. A calorimetric method was used for P2O5. Three Apollo 17 basalts, one Apollo 11 basalt, and one Apollo 15 basalt were used for the Ru-Os study. Os and Ru were measured in seven samples of breccia 14305 in a series of experiments to check an apparent anomaly in the isotopic composition of the Hg which it contains. A lunar model for Ru-Os partition is discussed. It is suggested that Ru and Os were partitioned and fractionated in the original differentiation of the lunar surface ocean. Fractionation among near-surface materials was less than a factor of 2 according to the lithic breccia data. Fractionations among basaltic sources were very large, exceeding 100, and primarily due to Ru. A clue to Ru and Os distributions at the depths from which mare basalts were derived may be provided by the relative ages of the basalts. These are interpreted as being related to partial melting in response to temperature increases at depth with time.

Jovanovic, S.↗

Grain size, petrographic, and FMR studies of the double core 60009/10 - A study of soil evolution

Six samples from the upper core 60010 of the double drive core 60009/60010 were analyzed for grain size distribution, petrographic particle types and abundances, magnetic fraction, and ferromagnetic resonance. It was found that the magnetic fraction of these soils is not equivalent to the agglutinate fraction, and magnetic separation partitions high-FeO agglutinate from low-FeO agglutinates. Various maturity indices are in essential agreement. The deposition of most or all of the core could have occurred in a single event. If that is the case, the core units have no time-stratigraphic significance and do not reflect individual cratering events.

Mckay, D. S.↗

Implications of liquid-liquid distribution coefficients to mineral-liquid partitioning

In order to evaluate the influence of a silicate liquid structure on mineral-liquid partitioning, element partitioning data is obtained for coexisting anhydrous immiscible granitic and ferrobasaltic magmas. It is found that: (1) mineral-liquid distribution coefficients indicate the competition of crystal and liquid for cation incorporation, (2) increased polymerization of the residual liquid during crystal-liquid fractionation increases the mineral-liquid distribution coefficients for high-charge-density cations, (3) incompatible element ratios of low- and high-charge-density cations may vary during crystal-liquid fractionation because of changes in the melt composition and structure, (4) relative solubilities of REE's in melts do not vary with melt polymerization, (5) the changes of Sm/Eu ratios during crystal-liquid fractionation depend on the melt composition, and (6) minor components and volatiles can significantly influence the silicate melt structure and the mineral-liquid distribution coefficients.

Ryerson, F. J.↗

On isotopic anomalies in samarium

The solar isotopic composition of Sm is decomposed into s, r, and p components. The anomaly pattern discovered by Lugmair et al. (1978) in EK1-04 Allende inclusion can be presented as a fractionation of the average s-pattern from the average r-pattern. This representation requires a fractionation of 0.029%/(amu) and either (1) a 0.42% deficiency of s relative to r and a 0.15% deficiency of p relative to r, or (2) a 0.42% excess of r relative to s and a 0.27% excess of p relative to s. The nature of this anomaly suggest a systematic physical fractionation of r, s, and p nuclei from each other in the initial condition leading to EK1-04. A neighboring supernova injection would not be expected to produce this anomaly.

Clayton, D. D.↗

Grain size and the evolution of Luna 24 soils

The grain size distribution of six Luna 24 samples has been determined. These samples are characterized by a bimodal distribution which is indicative of soils formed primarily by mixing rather than by reworking. Although agglutinate content decreases with depth, it is not likely that the Luna 24 soils have undergone appreciable in situ reworking. Particle types and abundances in each of four size fractions have been determined petrographically. Mineral fragments are very abundant in all analyzed size fractions. Pyroxene and plagioclase increase slightly in abundance at finer grain sizes, but olivine decreases significantly. Compared with typical mare soils, the Luna 24 trends are anomalous. They are compatible with the hypothesis than many, if not most, of the mineral grains in the 20-250-micron fractions come from coarse-grain rocks having average mineral grain sizes greater than 250 microns. The mineralogy and chemistry of the coarse-grained rocks has not been well characterized, but there is evidence that at least some of them are higher in MgO than the analyzed finer-grained basalts.

Mckay, D. S.↗

A two phase Mach number description of the equilibrium flow of nitrogen in ducts

Some additional thermodynamic properties of the usual two-phase form which is linear in the moisture fraction are derived which are useful in the analysis of many kinds of duct flow. The method used is based on knowledge of the vapor pressure and Gibbs function as functions of temperature. With these, additional two-phase functions linear in moisture fraction are generated, which ultimately reveal that the squared ratio of mixture specific volume to mixture sound speed depends on liquid mass fraction and temperature in the same manner as do many weighted mean two-phase properties. This leads to a simple method of calculating two-phase Mach numbers for various duct flows. The matching of one- and two-phase flows at a saturated vapor point with discontinuous Mach number is also discussed.

Bursik, J. W.↗

Isotopic anomalies of noble gases in meteorites and their origins. IV - C3 /Ornans/ carbonaceous chondrites

The C3O chondrites Kainsaz, Lance, and Ornans were studied by an acid dissolution technique to characterize the noble gas components in 3 mineral fractions: HF, HCl-solubles, chromite and carbon, and 'phase Q', a trace mineral containing Ar, Kr, Xe. For all fractions, gas contents decline in the order Kainsaz, Lance, Ornans; this trend parallels volatile contents but not heterogeneity of olivine composition or degree of metamorphism, and reflects progressively higher condensation temperature from the solar nebula. The Ar/Xe ratios and compositions of the three mineral fractions are discussed, and it is concluded that in all primitive chondrites the amount and the chemical separability of CCFXe parallel the abundance of primordial noble gases and other volatiles, such as C, N, Tl, Bi, and In. The close correlation of CCFXe with properties of local origin, such as volatile content and petrologic type, is more consistent with a local than with an extrasolar origin of the component.

Alaerts, L.↗

Thermodynamic analysis of turbulent combustion in a spark ignition engine. Experimental evidence

A method independent of physical modeling assumptions is presented to analyze high speed flame photography and cylinder pressure measurements from a transparent piston spark ignition research engine. The method involves defining characteristic quantities of the phenomena of flame propagation and combustion, and estimating their values from the experimental information. Using only the pressure information, the mass fraction curves are examined. An empirical burning law is presented which simulates such curves. Statistical data for the characteristics delay and burning angles which show that cycle to cycle fractional variations are of the same order of magnitude for both angles are discussed. The enflamed and burnt mass fractions are compared as are the rates of entrainment and burning.

Beretta, G. P.↗

User's guide for vectorized code EQUIL for calculating equilibrium chemistry on Control Data STAR-100 computer

A vectorized code, EQUIL, was developed for calculating the equilibrium chemistry of a reacting gas mixture on the Control Data STAR-100 computer. The code provides species mole fractions, mass fractions, and thermodynamic and transport properties of the mixture for given temperature, pressure, and elemental mass fractions. The code is set up for the electrons H, He, C, O, N system of elements. In all, 24 chemical species are included.

Kumar, A.↗

The origin of the 'FUN' anomalies and the high temperature inclusions in the Allende meteorite

The discovery of isotopic anomalies in white inclusions of the meteorite Allende has led to fundamental questions concerning the origin of these anomalies and of the white inclusions themselves. An analysis of the 'FUN' anomalies in the inclusions C1 and EK1-4-1 demonstrates that these isotopic anomalies may be decomposed into individual nucleosynthetic components, which have been subjected to separate mass and component fractionations. There is no evidence that any freshly-synthesized material injected into the primitive solar nebula was of abnormal isotopic composition, or that the FUN anomalies were due to an injection of unusual material. Rather, they show the effects of large mass fractionations and an unusual mixture of normal nucleosynthetic material, likely to be in the form of interstellar grains whose size or chemistry served as a memory for the nucleosynthetic origins of their constituent atoms. Giant gaseous protoplanets, as described for the early solar nebula by Cameron (1978), are a potential site for achieving both mass and component fractionations, and for producing white inclusions in general.

Consolmagno, G. J.↗

Are sulfur isotope ratios sufficient to determine the antiquity of sulfate reduction

Possible limitations on the use of sulfur isotope ratios in sedimentary sulfides to infer the evolution of microbial sulfate reduction are discussed. Current knowledge of the ways in which stable sulfur isotope ratios are altered by chemical and biological processes is examined, with attention given to the marine sulfur cycle involving various microbial populations, and sulfur reduction processes, and it is noted that satisfactory explanations of sulfur isotope ratios observed in live organisms and in sediments are not yet available. It is furthermore pointed out that all members of the same genus of sulfate reducing bacteria do not always fractionate sulfur to the same extent, that the extent of sulfur fractionation by many sulfate-reducing organisms has not yet been determined, and that inorganic processes can also affect sulfur isotope fractionation values. The information currently available is thus concluded to be insufficient to determine the time of initial appearance of biological sulfate reduction.

Ashendorf, D.↗

Sputtered silicon nitride coatings for wear protection

Silicon nitride films were deposited by RF sputtering on 304 stainless steel substrates in a planar RF sputtering apparatus. The sputtering was performed from a Si3N4 target in a sputtering atmosphere of argon and nitrogen. The rate of deposition, the composition of the coatings, the surface microhardness and the adhesion of the coatings to the substrates were investigated as a function of the process parameters, such as: substrate target distance, fraction nitrogen in the sputtering atmosphere and sputtering pressure. Silicon rich coating was obtained for fraction nitrogen below 0.2. The rate of deposition decreases continuously with increasing fraction nitrogen and decreasing sputtering pressure. It was found that the adherence of the coatings improves with decreasing sputtering pressure, almost independently of their composition.

Grill, A.↗

Foraging westward for pristine nonmare rocks - Complications for petrogenetic models

New advances are reported concerning an investigation which is being conducted to find and characterize more 'pristine' (compositionally endogenous) lunar rocks. Eleven nonmare samples are characterized petrographically and (except for two clasts that were prohibitively small) by chemical composition. The samples are assessed whether they are pristine on the basis of diagnostic features discussed by Warren and Wasson (1977). Five samples are found to be almost certainly pristine. They include the alkali-rich anorthosite 12073c, the troctolite 14179c, the anorthositic troctolite 14321c1, the troctolitic anorthosite 14321c2, and the anorthositic norite 15565c. Correlations between petrochemistry and longitude are also investigated, taking into account Eu fractionations, Sc-Ti-Sm fractionations, and Ca/Na-Mg/Fe fractionations.

Warren, P. H.↗

A chemical study of individual green glasses and brown glasses from 15426 - Implications for their petrogenesis

Systematic chemical analyses of individual Apollo 15 green glasses were performed in order to: (1) study chemical variations among them; (2) understand their petrogenesis and source region; and (3) study their possible relationships with mare basalts in general. Brown glasses were also analyzed in order to study their chemical variations and their petrogenetic relationships to green glasses and mare basalts. The chemical composition of green and brown glasses is shown and variation diagrams of Sc, Cr2O3, FeO, and Co abundances in green glasses are presented. Igneous fractionation, two component magma mixing, and partial melting of heterogeneous source materials are alternate scenarios to explain strong observed correlations. The composition of green glasses indicates that they were derived by partial melting of the fractionated cumulate source materials formed from a magma ocean which had experienced certain degrees of olivine and plagioclase fractional crystallization.

Ma, M.-S.↗

Noble gas trapping by laboratory carbon condensates

Trapping of noble gases by carbon-rich matter was investigated by synthesizing carbon condensates in a noble gas atmosphere. Laser evaporation of a solid carbon target yielded submicron grains which proved to be efficient noble gas trappers (Xe distribution coefficients up to 13 cu cm STP/g-atm). The carbon condensates are better noble gas trappers than previously reported synthetic samples, except one, but coefficients inferred for meteoritic acid-residues are still orders of magnitude higher. The trapped noble gases are loosely bound and elementally strongly fractionated, but isotopic fractionations were not detected. Although this experiment does not simulate nebular conditions, the results support the evidence that carbon-rich phases in meteorites may be carriers of noble gases from early solar system reservoirs. The trapped elemental noble gas fractionations are remarkably similar to both those inferred for meteorites and those of planetary atmospheres for earth, Mars and Venus.

Niemeyer, S.↗

Sorption of noble gases by solids, with reference to meteorites. II - Chromite and carbon. III - Sulfides, spinels, and other substances; on the origin of planetary gases

The trapping of noble gases by chromite and carbon, two putative carriers of primordial noble gases in meteorites, was studied by synthesizing 19 samples in a Ne-Ar-Kr-Xe atmosphere at 440-720 K. Noble gas contents are found to approximately obey Henry's Law, but only slight correlations are found with composition, surface area, or adsorption temperature. Geometric mean distribution coefficients for bulk samples and HCl residues in 10 cu cm STP/g atm are: Xe 100, Kr 15, Ar 3.5, and Ne 0.62. Elemental fractionation data support the suggestion of Lewis et al. (1977) that chromite and carbon in C2 and C3 chondrites were formed by the reaction: Fe, Cr + 4CO yields (Fe, Cr)3O4 + 4C + carbides. In contrast to meteoritic minerals, the synthetic specimens show no isotopic fractionation of noble gases. In a subsequent study, attention is given to the cases of sulfides and spinels, on the way to consideration of the origin of planetary gases. Sulfides showed three distinctive trends relative to chromite or magnetite. The elemental fractionation pattern of Ar, Kr and Xe in meteorites, terrestrial rocks and planets resembles the adsorption patterns on the carbons, spinels, sulfides, and other solids studied. The high release temperature of meteoritic noble gases may be explained by transformation of the physisorbed or chemisorbed gas. The ready loss of meteoritic heavy gases on surficial oxidation is consistent with adsorption, as is the high abundance.

Yang, J.↗

Chemical composition of cometary nuclei

Observational evidence pertaining to the origin and composition of cometary material is reviewed. Arguments favoring the undifferentiated character of the icy conglomerate are summarized. Theoretical descriptions of the sublimation of a cometary nucleus and the velocity field of the expanding gas are presented and compared with observations. The nature of cometary dust and the atomic abundances of H, C, N, O, and S in the volatile fraction are examined, and data on the dust and volatile fractions are combined to derive elemental abundances. It is shown that O, N, and S in cometary nuclei appear to have essentially cosmic abundances but that both H and C are drastically depleted with respect to the cosmic abundances. The apparent depletion of C by a factor of more than three is discussed. It is suggested that the missing carbon might be hidden in the dust fraction in the form of heavy organic molecules or might have remained in either the primeval solar nebula or interstellar space.

Delsemme, A. H.↗