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At least 181 records · Page 10

Textural evidence bearing on the origin of isolated olivine crystals in C2 carbonaceous chondrites

In some cases the mechanical competence of chondrules in carbonaceous chondrites has been reduced by alteration of their mesostasis glass to friable phyllosilicate, providing a mechanism by which euhedral olivines can be separated from chondrules. Morphological features of isolate olivine grains found in carbonaceous chondrites are similar to those of olivine phenocrysts in chondrules. These observations suggest that the isolated olivine grains formed in chondrules, by crystallization from a liquid, rather than by condensation from a vapor.

Richardson, S. M.↗

Vein formation in the C1 carbonaceous chondrites

Veins in the C1 chondrites Orgueil, Alais, and Ivuna have been deposited during an extended period of impact brecciation and leaching. At least three generations of mineralization, dominated successively by carbonates, calcium sulfate, and magnesium sulfate, can be recognized. Vein minerals are derived locally by closed-system reactions between matrix phyllosilicates and an aqueous fluid, with the result that few, if any, primitive mineral phases still exist in the C1s.

Richardson, S. M.↗

On the kinetics of volatile loss from chondrites

Data by Lipschutz and coworkers (1975, 1976, 1977) on thermal release of Tl, Bi, and In from primitive chondrites are reexamined to obtain information on the nature and activation energy (E) of release processes: desorption, volume diffusion, and decomposition of the host phase. For the Allende C3 chondrite, the main release for Bi and Tl between 400 and 700 C is shown to be apparently due to desorption of a surface layer, coupled with grain boundary diffusion as the slow step. Further, the main release of In above 600 C and the small tails of Bi and Tl between 700 and 1000 C are observed to represent probably volume diffusion. Results for Abee and other primitive meteorites were found to be essentially similar, except for a very abrupt 500 C release of Tl from Krymka (81%) and Bi from Tieschitz (70%). It is suggested that this release may represent decomposition of a thermolabile phase in a late condensate, such as organic matter or phyllosilicates.

Alaerts, L.↗

Carbonaceous chondrites. I - Characterization and significance of carbonaceous chondrite /CM/ xenoliths in the Jodzie howardite

Mineralogical, chemical, textural, and isotopic studies of the abundant carbonaceous inclusions in the Jodzie howardite which are consistent with carbonaceous chondrite (CM) characteristics are examined. These CM xenoliths show regolith alteration comparable to the Murray and Murchison meteorites but less than Nogoya, flow-oriented development of phyllosilicates and 'poorly characterized phases', and partial oxidation of sulfides. Temperature-programmed pyrolysis mass spectrometry indicates that gas release patterns of volatiles and hydrocarbons, and N, C, and S contents are typical of CM meteorites. The fact that the Ne content is typical for 'solar' values and the isotopic structure of Xe is 'planetary' indicates that these gases were entrapped by different mechanisms, and cosmic ray exposure ages for the xenoliths agree with the reported exposure age for the eucritic host.

Bunch, T. E.↗

Alteration in CM carbonaceous chondrites inferred from modal and chemical variations in matrix

The modal abundance of matrix in CM chondrites appears to vary from 57-85 vol%. The concentrations of volatile elements that should occur in matrix remain approximately constant despite differences in the proportions of matrix, suggesting that the differing matrix contents may not be real primary variations but are optical effects due to aqueous alteration processes that make other petrologic components unrecognizable. Apparent matrix content can be used as a qualitative measure of the degree of alteration experienced by each CM chondrite. Fe/Si ratios in matrices decrease progressively with increasing alteration due to the formation of new phyllosilicate phases with higher Mg/Fe ratios and optically recognizable opaque minerals that are not counted as matrix. The aqueous alteration process in CM chondrites appears to have been largely isochemical if the bulk meteorites are considered as the reacting systems, although depletion patterns and isotopic anomalies indicate open-system behavior for a few highly mobile components.

Mcsween, H. Y., Jr.↗

Intergrown mica and montmorillonite in the Allende carbonaceous chondrite

High resolution transmission electron microscopy (HRTEM) observations were made of a mixture of mica and montmorillonite from fine-grained calcium, aluminum inclusions (CAI) in the Allende C3(V) meteorite. A petrographic thin section having a diameter of 4 mm contained CAI fragments ranging from less than 1 to 50 microns. The observed textural and chemical characteristics placed the inclusion in the fine-grained alkali-rich spinel aggregate category of Warks' (1979) classifications of CAIs and as type 3 in Kornacki's classifications of fine grains in Allende. Chemical analyses were performed on the phyllosilicate grains observed in the TEM scan by means of an X ray observed, and the proximity to the matrix boundary suggests a metamorphism which included aqueous alteration at a relatively low temperature.

Tomeoka, K.↗

FeO and H-2O and the homogeneous accretion of the earth

Shock devolatilization recovery data for brunite (Mg(OH)2) shocked to 13 and 23 GPa are presented. These data combined with previous data for serpentine (Mg3Si2O5(OH)4) are used to constrain the minimum size terrestrial planet for which planetesimal infall will result in an impact generated water atmosphere. Assuming, in hydrous phyllosilicates, model calculations simulating the interaction of metallic iron with impact released free water on the surface of the accreting Earth were carried out. It is assumed that the reaction of water with iron in the presence of enstatite is the prime source of the terrestrial FeO component of silicates and oxides. Lower and upper bounds on the terrestrial FeO budget are based on mantle FeO content and possible incorporation of FeO in the outer core. We demonstrate that the iron water reaction would result in the absence of atmospheric/hydrospheric water, if homogeneous accretion is assumed.

Lange, M. A.↗

Mineralogy and petrology of chondrules and inclusions in the Mokoia CV3 chondrite

The inclusions and chondrules of the Mokoia CV3 chondrite are studied systematically and compared with those in the Allende meteorite. Five polished thin sections of Mokoia were examined by optical microscopy, backscattered scanning electron microscopy, and electronprobe microanalysis, and objects greater than about 100 microns in apparent diameter were measured and classified petrographically. Three major types of olivine chondrules are distinguished: igneous chondrules, which evidently crystallized from droplets of silicate melt; recrystallized chondrules, apparently metamorphosed at relatively high temperatures; and accretional aggregates, which are probably fragments of igneous chondrules. Refractory inclusions in Mokoia are generally similar to those found in Allende, although Mokoia inclusions include phyllosilicates rather than feldspathoids and melilite-rich Ca, Al-rich inclusions (CAIs) are more abundant in Allende. The small, fine-grained CAIs, which are more abundant than coarse-grained CAIs in both meteorites, are observed to represent aggregates of three distinct constituents: concentric objects, chaotic material and inclusion matrix. It is concluded that most of the CAIs probably formed during metamorphism, partial melting, and incomplete distillation of primitive dust aggregates heated in the solar nebula.

Cohen, R. E.↗

A new layered mineral from the Mighei carbonaceous chondrite

The poorly characterized phase (PCP) of the Mighei CM2 carbonaceous chondrite is investigated using high-resolution TEM. Electron-microprobe analyses of samples from both olivine chondrules and the matrix are included in a table. Chondrule PCP is found to have higher concentrations of S and Ni and lower concentrations of Si, Mg, and Al than matrix PCP. TEM shows that PCP in this chondrite is an intergrowth of three phases (in various proportions): a major component containing Fe, S, Ni, and O in wavy rolled layers spaced about 5.4 A apart, an Fe-rich serpentinelike phyllosilicate with 7-A layer spacing, and submicron grains of magnetite, chromite, and phosphate. It is proposed that chondrule PCP contains mainly the 5-A phase with some grains, while matrix PCP consists mostly of the 5-A and 7-A phases.

Tomeoka, K.↗

Mineralogical-petrological characterization of near-earth asteroids

The mineralogy and petrology of 17 near-earth asteroids are characterized using reflectance spectroscopy with ground-based telescopes. Assuming the surfaces are composed of cosmically abundant materials, the presence of certain mineralogical species can be determined from diagnostic absorption features and spectral characteristics which have been studied under known laboratory conditions and understood in terms of crystal-field theory. With one possible exception, the surface composition of near-earth asteroids consists of common rock-forming minerals such as olivine, pyroxene, and phyllosilicates. Opaque components are present but cannot be mineralogically identified with existing experimental data. The spectrum of 2201 Oljato cannot be interpreted in terms of common rock-forming minerals and is examined for cometary features because its high orbital eccentricity suggests a possible relation to comets, but no common cometary features are identified. The predominance of mafic silicate absorption features in spectra of near-earth asteroids (compared to the majority of main-belt asteroids) may be a primary compositional feature or may be the signature of relatively fresher asteroid material.

Mcfadden, L. A.↗

FeO and H2O and the homogeneous accretion of the earth

Shock devolatilization recovery data for brunite (Mg(OH)2) shocked to 13 and 23 GPa are presented. These data combined with previous data for serpentine (Mg3Si2O5(OH)4) are used to constrain the minimum size terrestrial planet for which planetesimal infall will result in an impact generated water atmosphere. Assuming, in hydrous phyllosilicates, model calculations simulating the interaction of metallic iron with impact released free water on the surface of the accreting earth were carried out. It is assumed that the reaction of water with iron in the presence of enstatite is the prime source of the terrestrial FeO component of silicates and oxides. Lower and upper bounds on the terrestrial FeO budget are based on mantle FeO content and possible incorporation of FeO in the outer core. We demonstrate that the iron water reaction would resuit in the absence of atmospheric/hydrospheric water, if homogeneous accretion is assumed.

Lange, M. A.↗

Layer silicates in a chondritic porous interplanetary dust particle

Analytical electron microscopy on individual grains from a portion of a chondritic porous interplanetary dust particle (aggregate W7029C1 from the NASA Johnson Space Center Cosmic Dust Collection) shows that layer silicates compose 50 percent of the silicate fraction examined. These layer silicates can be classified into two distinct crystallochemical groups: (1) fine-grained, polycrystalline smectite minerals; and (2) well-ordered, single crystals of kaolinite and Mg-poor talc. The layer silicates in this portion of sample W7029(asterisk)A are dissimilar to those described in other chondritic porous aggregates. The predominant layer silicate assemblage in W7029(asterisk)A indicates that heating of the aggregate during atmospheric entry was brief and probably to a temperature less than 300 C. Comparison with terrestrial phyllosilicate occurrences suggests that some layer silicates in aggregate W7029(asterisk)A may have been formed by alteratiton from preexisting silicate minerals at low temperatures (less than 25 C) after aggregate formation.

Rietmeijer, F. J. M.↗

Terrestrial analogues of the surface rocks of Mars?

Evidence is presented which suggests that hisingerite, iddingsite, and several ferric sulfate minerals derived from deuteric alteration of iron-rich basalts on earth may provide clues to the evolutionary history of the surface of Mars. The characteristics of these minerals are pointed out, and their strong compositional and paragenetic similarities to Martian regolith materials are pointed out. These similarities are consistent with a mineral assemblage on Mars consisting of ferric-bearing phyllosilicate, sulfate, and oxyhydroxide phases. These phases could have been derived from postmagmatic deuteric alteration of volatile-rich iron-rich basaltic rocks containing fayalitic olivine, Fe pyroxenes, and accessory pyrrhotite.

Burns, R. G.↗

Infrared observations of planets

A positive correlation was found between the strength of the 3-micron water feature and the strength of the absorption feature shortward of 0.4 microns. This is similar to what is seen in laboratory spectra of carbonaceous chondrites whose silicate compositions range from hydrated phyllosilicates to anhydrous olivine. Features were found in the IRAS images that appear to be related to solar system objects. Analysis of the data has yielded narrow trails of dust coincident with the orbits of comets Temple 2, Encke, and Gunn. Dust is found both ahead and behind comet orbital positions due to low-velocity ejection of large particles during perihelion passage. The occultation diameters of Ceres and Pallas were used to improve the standard thermal model used in the reduction of thermal IR observations of asteroids.

Lebofsky, L. A.↗

Weathering of sulfides on Mars

Pyrrhotite-pentlandite assemblages in mafic and ultramafic igneous rocks may have contributed significantly to the chemical weathering reactions that produce degradation products in the Martian regolith. By analogy and terrestrial processes, a model is proposed whereby supergene alteration of these primary Fe-Ni sulfides on Mars has generated secondary sulfides (e.g., pyrite) below the water table and produced acidic groundwater containing high concentrations of dissolved Fe, Ni, and sulfate ions. The low pH solutions also initiated weathering reactions of igneous feldspars and ferromagnesian silicates to form clay silicate and ferric oxyhydroxide phases. Near-surface oxidation and hydrolysis of ferric sulfato-and hydroxo-complex ions and sols formed gossan above the water table consisting of poorly crystalline hydrated ferric sulfates (e.g., jarosite), oxides (ferrihydrite, goethite), and silica (opal). Underlying groundwater, now permafrost contains hydroxo sulfato complexes of Fe, Al, Mg, Ni, which may be stabilized in frozen acidic solutions beneath the surface of Mars. Sublimation of permafrost may replenish colloidal ferric oxides, sulfates, and phyllosilicates during dust storms on Mars.

Burns, Roger G.↗

Aqueous alteration in carbonaceous chondrites - Mass balance constraints on matrix mineralogy

Bulk chemical compositions of matrix material were determined in eleven Antarctic CM chondrites and five non-Antarctic CM and CI chondrites, using microprobe defocused-beam technique. The results, along with previously published data, are used to provide mass balance constraints on the relative proportions of intergrown and intermixed phyllosilicate phases in carbonaceous chondrite matrices. In terms of Fe, Si, and Mg, the CM matrix bulk compositions plot within a triangle defined by the compositions of PCP (a mixture of 25 percent tochilinite and 75 percent cronstedtite), Mg-rich serpentine, and Fe-rich serpentine. Results indicate differing amounts of PCP and serpentines in individual CM matrices. The discrepancies found between predicted and measured S and Ni values require additional sulfide phases. CI matrices were found to contain little, if any, PCP; they consist mostly of serpentine and montmorillonite.

Mcsween, Harry Y., Jr.↗

Murchison xenoliths

C3 xenoliths in a C2 host (Murchison) are unique among known meteoritic xenolith-host occurrences. They offer an opportunity to determine possible effects on the xenoliths by the hydrated host. Eleven xenoliths were found ranging from 2 to 13 mm. Four of these Murchison Xenoliths (MX1, MX2, MX3 and MX4) have been studied in detail. MX1 and MX2 were large enough for trace element, oxygen isotope, carbon isotope, bulk carbon and bulk nitrogen determinations. All four were studied petrographically and by analytical SEM. The xenoliths cannot be unequivocally identified as C3V or C3O subtypes. MX1 contains some matrix phyllosilicate, indicating reaction with water. MX1, MX2 and MX3 all show extensive alteration by an FeO-rich medium, and some minerals in them contain ferric iron. MX4, however, exhibits very minor alteration by FeO only. Oxygen isotopic and chemical data show that the alteration of these xenoliths did not take place in the Murchison host. The alterations occurred in one or more parent bodies, which were later disrupted to release these xenoliths that ultimately accreted onto the Murchison parent body.

Olsen, Edward J.↗

Matrix mineralogy of the Orgueil CI carbonaceous chondrite

This paper presents the results of petrographic, SEM, and TEM studies of the matrix minerals in Orgueil. It was found that the matrix consists mainly of Fe-bearing Mg-rich serpentine and saponite, and a poorly crystallized Fe-rich ferrihydrite containing small and varying amounts of S and Ni. The serpentine and saponite, which occur in roughly equal molar proportions, are coherently intergrown and occur mainly in fine phyllosilicates in intimate association with the ferrihydrite. Coarse phylosilicates occur in clusters relatively free of ferrihydrite. The matrix mineralogy of the Orgueil chondrite suggests that Orgueil experienced considerably different alteration conditions than did the CM chondrites.

Tomeoka, Kazushige↗