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Core binding energy difference between bridging and nonbridging oxygen atoms in silicate chain of pyroxenes, using X ray photoelectron spectra
Interstellar silicate absorption search using VI Cyg No 12 spectrum observations
Tranquillityite silicate mineral in crystalline basaltic rocks from Apollo 11 and 12 samples
Hugoniot measurements on iron-silicate garnet demonstrate that above a shock pressure of about 205 kbar transition to a high-pressure phase(s), having an apparent zero-pressure density and bulk modulus of 4.44 g/cu cm and 3.3 Mbar, occurs. Crystal chemical systematics and Debye-Scherrer X-ray patterns of a recovered phase(s), which may be the shock-induced high-pressure form, suggest possible formation of a phase with a density of 4.48/cu cm. Occurrence of such a polymorph of garnet in the mantle would give rise to an increase in density and seismic velocity below 600 km in the earth.
Experimental finding is that mass absorption coefficient is independent of frequency but highly dependent on moisture content; effective conductivity increases with frequency, and low tangent is independent of frequency. Computed values of electrical properties are in rough numerical agreement with extrapolated laboratory values on other silicate materials.
The partitioning of potassium between roedderite, K2Mg5Si12O30 and an Fe-FeS melt was investigated at temperatures about 40 C above the Fe-FeS eutectic. Roedderite was considered a prime candidate for one of the potassium-bearing phases in the primitive earth because roedderite and merrihueite are the only two silicates containing essential potassium which have been identified in stony meteorites. Application of the results to a primitive chondritic earth is discussed, and it is concluded that extraction of most of the earth's potassium into the Fe-FeS core would occur under the conditions in the early earth.-
The exact calculation of scattering and absorption by various sub-micron sized silicate spheres is presented here, using accurately determined optical constants in the wavelength range from 50 to 0.21 microns. The extinction features near 10 and 20 microns for various samples are discussed. It is found that the ratio of peak extinction at 20 microns to that at 10 microns is constant for small particles up to 0.4-micron radius, but is less for particles of 1-micron radius. The ratio of maximum extinction in the ultraviolet to that at 10 microns decreases with increasing particle size.
Formulations and general procedures are given for making and applying space environmentally, as well as atmospherically stable black silicate paints. Compositions are given which meet spacecraft self-contamination requirements, have excellent heat resistance, and are strongly semiconductive.
The partitioning of potassium between roedderite, K2Mg5Si12O30 and an Fe-FeS melt was investigaged at temperatures about 40 C above the Fe-FeS eutectic. Roedderite was considered a prime candidate for one of the potassium-bearing phases in the primitive earth because roedderite and merrihueite are the only two silicates containing essential potassium which have been identified in stony meteorites. A mean K2S/FeS weight ratio of (3.340 + or - 0.015) x 0.001 was determined in these experiments; a K2S/FeS weight ratio of about 0.01 would be sufficient to extract all potassium in a chondritic earth into the core. Application of these results to a primitive chondritic earth is discussed and it is concluded that extraction of most of the earth's potassium into the Fe-FeS core would occur under the conditions in the early earth.
Experiments were performed on silicate compositions in the forsterite-anorthite-silica and forsterite-anorthite-diopside systems to determine the relative amounts of Cr(II), Cr(III), and Cr(VI) over a wide range of oxygen partial pressures from 10 to the -10th to 1 atm at 1500 and 1550 C. Redox states were measured by visible absorption spectroscopy and electron paramagnetic resonance spectroscopy and titration. It was found that Cr is present almost exclusively as Cr(III) in terrestrial basaltic liquids and as a mixture of Cr(III) and Cr(II) in lunar basaltic liquids.
Trace-element concentrations in separated minerals and rock fragments from a coarsely crushed and sieved sample of medium-grained lunar basalt are determined by high-precision instrumental neutron activation analysis for three main purposes. These are: (1) to test a previously proposed model for describing trace-element behavior during solidification of a silicate liquid under conditions of a closed system; (2) to compare trace-element concentrations among different size fractions of a comminuted basalt; and (3) to investigate small-scale heterogeneity within a single medium-grained basalt. It is found that an excellent mass balance for the whole rock is attained in terms of the trace-element concentrations of the component minerals and mesostasis, that the mixing model describing this mass balance yields a superior modal analysis for the whole rock, and that different size fractions of the coarsely crushed basalt vary in mineral composition. The closed-system model is shown to account properly for the average behavior of the trace elements during solidification of the basalt, and values of distribution coefficients are obtained for incompatible elements in that rock.
Amorphous magnesium silicate smoke particles were condensed from hydrogen and argon atmospheres containing Mg and Si0. A wide range of initial compositions were observed but all particles could be recrystallized into forsterite (Mg2Si04), by heating to 1000 C in vacuum. The amount of smoke formed decreased rapidly with temperatures between 300 and 800 K at reactant partial pressures of about 1 torr.
Near-normal incidence reflectance measurements in the interval 1026-1640 A were performed on four silicates already studied in the visible and infrared. A Kramers-Kronig analysis of these data is used to calculate the complex index of refraction m = n - ik. New transmission measurements improve the determination of k in the interval 2500-4500 A, except for andesite, which is more opaque than had been previously observed.
Laboratory reflection polarimetry is presented for eight samples of artificial, poorly crystalline magnesian silicates with varying admixtures of carbon black. The polarimetric slope-albedo law saturates for geometric albedos lower than about 0.05, and good agreement with the telescopic polarization-phase curves of C-type asteroids is found for albedos as low as 0.02. Thus the conclusion from thermal radiometry is confirmed that the C objects are very dark, darker than any known carbonaceous chondrite.
Distribution coefficients have been found for the partitioning of Ni, Co, and Mn between calcium-rich clinopyroxenes and coexisting silicate liquids. Values are found for the 1110-1360 C temperature range. The breakdown of Henry's Law was not observed. The measured clinopyroxene/liquid distribution coefficients ranged from 1.5-14.0 for Ni, 0.5-2.0 for Co, and 0.3-1.2 for Mn. Analyses of pyroxenes grown from charges differing in the amounts of transition metals indicate that Ni and Co occupy the M1 site of diopside and that Mn occupies the M1 and M2 sites. Equilibrium constants were found in terms of the activities of the components in the liquid and solid phases. These activities are based on the mole fractions. An activity/concentration model was used for the liquid phase in order to explain the variations in the clinopyroxene/liquid coefficients due to bulk composition.
Primary silicate melt inclusions in ilmenite crystals in seven mare basalt samples were analyzed by electron microprobe, and analyses were made of their host and associated phases. Two distinct and restricted chemical composition ranges are drawn: high-K and low-K. The high-K samples are nearly identical with the granitic residual liquid, averaging a weight percentage of 6.27% K20, 76.3% SiO2, plus 82% normative quartz and orthoclase. It is noted that no low-K melt was found as a re-entrant or interstitial inclusion in any sample; only as isolated inclusions in illmenite.
Silicate spherules larger than 100 microns were extracted from 100 kg of box core samples of Pacific red clay taken in the mid-Pacific at a depth of 5 km, and the concentration of nonvolatile trace elements was determined for three spheres. One of the spheres shows excellent resemblance to C1 chondrite nonvolatile trace-element abundance patterns, and the relative abundances of the other two spheres are also very similar to those of C1 chondrites. One of these two spheres is depleted in Ir and Ru, while the other is depleted for Ni and Cr; possible explanations for the depletions are considered. Since the elemental abundances of the third sphere match the abundances of C1 chondrites, it is suggested that this sphere must be of extraterrestrial origin.
A paint binder is described which uses a potassium or sodium silicate dispersion having a silicon dioxide to alkali-metal oxide mol ratio of from 4.8:1 to 6.0:1. The binder exhibits stability during both manufacture and storage. The process of making the binder is predictable and repeatable and the binder may be made with inexpensive components. The high mol ratio is achieved with the inclusion of a silicon dioxide hydrogel. The binder, which also employs a silicone, is in the final form of a hydrogel sol.