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All sourcesNASA NTRSDOE OSTI
NASA NTRS1981

Chondrules in H3 chondrites - Textures, compositions and origins

Compositional and textural variations among chondrules in unequilibrated (type 3) H-group chondrites are examined in order to determine possible relations between chondrule compositions and textures. Bulk compositions of polished thin sections of 90 individual chondrules and 16 compound chondrule sets from the Sharps, Tieschitz and Bremervorde chondrites were measured by broad-beam electron probe analyses; the chondrules were also classified petrographically as barred olivine, porphyritic olivine, porphyritic pyroxene, barred pyroxene, radiating pyroxene or fine-grained. The mean compositions of each type are found to be distinct as verified by discriminant analysis, despite a large scatter, with the olivine-rich chondrules characterized by low SiO2 and high FeO and MgO contents, greater concentrations of TiO2, Al2O3, Na2O and K2O, and lower Cr2O3 and MnO relative to pyroxene-rich chondrules. Data suggest that composition, together with cooling rate, has played a conspicuous role in producing observed chrondrule textures, and are consistent with chondrule formation from mixtures of differing fractions of high-, intermediate- and low-temperature nebular condensates that underwent melting in space.

Lux, G.↗
NASA NTRS1981

Method of preventing oxidation of graphite fireproof material

A method of preventing oxidation of graphite fireproof material is given. A blend of 1 to 33 weight parts alumina and 3 to 19 parts of K2O + Na2O in 100 parts of SiO2 is pulverized followed by addition of 5 to 160 parts of silicon carbide powder in 100 parts of the mixture. This is thoroughly blended and coated on the surface of graphite fireproof material.

Yamauchi, S.↗
NASA NTRS1981

Derivation of a heterogeneous lithic fragment in the Bovedy L-group chondrite from impact-melted porphyritic chondrules

Results are presented of petrographic, compositional and dating analyses of a light-colored lithic fragment in the L-group Bovedy meteorite that has a composition different from that of the host chondrite. Polished thin sections of the lithic fragment, host, and the fragment-host boundary were examined microscopically and analyzed by electron microprobe, metallic Ni-Fe, and instrumental neutron activation techniques; chips of the fragment were also used for Ar-39/Ar-40 dating and oxygen isotope analyses. The poikilitic textures, olivine, low-Ca pyroxene and kamacite composition and low Na2O, K2O and P2O5 contents of the fragment indicate that it represents a solidified, slightly fractionated impact melt formed from a source rich in porphyritic chondrules. A progressive increase on MgO content across the fragment is accounted for by the heterogeneous nucleation of MgO-rich phases. The Ar data indicate that the Bovedy lithic fragment and its host were partly degassed of radiogenic Ar less than 0.94 billion years ago, probably due to shock. The data are consistent with a cooling rate of about 5 C/million years through 500 C, which must have resulted from the burial of the assemblage beneath insulating material on the parent body at depths of at least several km.

Rubin, A. E.↗
NASA NTRS1982

The relationship of the lunar regolith less than 10-microns fraction and agglutinates. II - Chemical composition of agglutinate glass as a test of the 'fusion of the finest fraction' /F3/ model

Agglutinate glasses from nine Apollo soils have been studied using an automated electron microprobe technique in order to test the fusion of the finest fraction model proposed by Papike (1981). The nine average agglutinate glass compositions are compared with the calculated fused-soil-free compositions, the bulk compositions and the 90-20 micron fraction compositions of the soils in which they are found. It is found that the agglutinate glass data are consistent with the composition of most of the fractions finer than 10 microns, allowing for the volatile loss of K2O and Na2O; some inconsistencies that do arise may result from the degree of soil maturity and the amount of material finer than 10 microns. It is concluded that the fusion of the finest fraction model is a good first approximation of mechanisms affecting the formation of agglutinate glass.

Walker, R. J.↗
NASA NTRS1982

The lunar regolith - Chemistry, mineralogy, and petrology

The data base on the lunar regolith is surveyed to form a synthesis of the lunar regolith chemistry, mineralogy, and petrology. The data were derived from samples collected by the Apollo missions 11-17 and the Luna 16, 20, and 24 probes. The missions were sent to sample formations and areas which typified the common observed features of the lunar surface. Drive tubes were used to extract samples from beneath the surface in order to study the relationship between the regolith and the bedrock, as well as to identify the processes that formed the regolith, which is regarded as the prime source of raw materials for early lunar industrial activities. Regolith origins are now understood to be destructive processes of comminution and constructional processes of agglutinate formation. Mixing occurs on the local scale, although lateral transport is inefficient on the moon. The usual contents of the fraction of regolith less than 10 microns in diameter are Al2O3, CaO, Na2O, K2O, light REE, and Th.

Papike, J. J.↗
NASA NTRS1983

Stillwater anorthosites - A lunar analog?

Samples of anorthosite from Stillwater complex units AN-I and AN-II have been studied by instrumental neutron activation analysis for FeO, CaO, Na2O, REE, and other trace elements, and the results are discussed. No systematic variations of chemical composition with stratigraphic position were observed. The major and trace compositions of both units appear to be identical, with plagioclase compositions virtually constant throughout both. Thus, there is almost no evidence for evolution of parent magma composition during the genesis of these units. The bulk of the anorthosites appear to consist of cumulus-adcumulus plagioclase and pyroxene. Very little trapped liquid component was found. The chemical elements are not normally or lognormally distributed among samples taken from either anorthosite unit. The irregular distribution of pyroxene oikocrysts indicates that interstitial melt migrated substantially prior to final consolidation of the rock.

Salpas, P. A.↗
NASA NTRS1983

Morphology and chemistry of projectile residue in small experimental impact craters

Small-scale impact craters (5-7 mm in diameter) were produced with a light gas gun in high purity Au and Cu targets using soda lime glass (SL) and man-made basalt glass (BG) as projectiles. Maximum impact velocity was 6.4 km/s resulting in peak pressures of approximately 120-150 GPa. Copious amounts of projectile melts are preserved as thin glass liners draping the entire crater cavity; some of this liner may be lost by spallation, however. SEM investigations reveal complex surface textures including multistage flow phenomena and distinct temporal deposition sequences of small droplets. Inasmuch as some of the melts were generated at peak pressures greater than 120 GPa, these glasses represent the most severely shocked silicates recovered from laboratory experiments to date. Major element analyses reveal partial loss of alkalis; Na2O loss of 10-15 percent is observed, while K2O loss may be as high as 30-50 percent. Although the observed volatile loss in these projectile melts is significant, it still remains uncertain whether target melts produced on planetary surfaces are severely fractionated by selective volatilization processes.

Horz, F.↗
NASA NTRS1984

Bulk compositions of Al-rich chondrules in ordinary and carbonaceous chondrites: Variations and similarities

An extended study of ordinary chondrites revealed that chondrules exist which are transitional in composition between Al-rich and Mg-Fe-rich types in contrast to the finding of Wlotzka, who inferred a gap in compositions between the Ca-Al-rich and Mg-Fe-rich chondrules. Transitional chondrule bulk compositions are plotted. They show that no compositional gap exists between the Mg-Fe-rich and Al-rich chondrules. Chondrules with Na2O-contents 3.0 wt.% are indicated. Variable CaO/Na2O-ratios for chondrule bulk compositions exist, similar to what was described for the subgroups of Al-rich chondrules. Al-rich and transitional chondrules similar to those described above were found also in carbonaceous chrondrites. Thirty-nine chondrules from the carbonaceous chondrites Leoville, Allende, Vigarano and Colony were investigated. Their bulk compositions in terms of Al2O3 vs. CaO were plotted.

Bischoff, A.↗
NASA NTRS1984

The Colony meteorite and the possible existence of a new chemical subgroup of CO3 chondrites

The Colony meteorite, found in Oklahoma around 1975, has an unrecrystallized texture and contains heterogeneous olivine and low Ca pyroxene, kamacite with low Ni and Co and high Cr, amoeboid inclusions with low FeO and MnO, and numerous small chondrules with clear pink glass. These characteristics are shared by members of the least metamorphosed subgroup of CO3 chondrites. Colony contains a fine grained matrix that has higher FeO and K2O and lower MgO and Na2O than normal CO3 matrices. Allan Hills A77307 is another unmetamorphosed meteorite that has many petrologic similarities to normal CO chondrites, including matrix abundance, mineral compositions and chondrule size. However, it differs from them in its abundance of magnetite and presence of iron carbides. The olivine and low Ca pyroxene compositional distributions of Colony and A77307 are very similar. The shapes of the thermoluminescence glow curves of Colony and A77307 are very similar, but differ significantly from those of normal CO chondrites. It is suggested that Colony and A77307 represent a distinct chemical subgroup of CO3 chondrites, characterized by low Ni, Co, S, Ca, Mg, Mn and, possibly, high Cd.

Rubin, A. E.↗
NASA NTRS1985

The Geology of East Butte, a Rhyolitic Volcanic Dome on the Eastern Snake River Plain, Idaho

East Butte is a prominent volcanic dome located on the eastern Snake River Plain. It is situated 51 km west of Idaho Fallls in the southeast corner of the Idaho National Engineering facility. East Butte rises 350 meters above the Quaternary basalt flows which encircle its 2.4 kilometer diameter base. Its maximum elevation is 2003 meters above sea level. East Butte is composed dominantly of rhyolite. Armstrong and others (1975) determined a K-Ar age of 0.6 +/- m.y. for a rhyolite sample from East Butte. Detailed geologic mapping revealed East Butte to be a single, large cumulo-dome composed dominantly of rhyolite. Major element geochemical analyses indicate that the rhyolite of East Butte is mildly peralkaline (molecular excess of Na2O and K2O over Al2O3 and compositionally homogeneous. Color variations in the East Butte rhyolite result from varying amounts of chemical and physical weathering and to the degree of devitrification that the glass in the groundmass of the rhyolite underwent.

Bretches, J. E.↗
NASA NTRS1987

Barred olivine chondrules in ordinary chondrites

The characteristics of 125 barred olivine chondrules identified in polished thin sections of 26 H-L-LL3-6 chondrites were studied, using an electron microprobe for determining mineral abundances and a broad-beam electron microprobe for determining bulk compositions. Compared with all chondrule types in the H-L-LL3 ordinary chondrites, the barred olivine chondrules were found to be enriched in FeO, Al2O3, Na2O, and K2O and depleted in SiO2 and MgO; they were also found to be enriched in the feldspathic component. It is concluded that the precursor components of barred olivine chondrules consisted of a mixture of an olivine-rich component, a refractory-rich component containing Al2O3, TiO2, and CaO, and a volatile-rich alkalic component. This unusual combination implies high temperatures of melting for the refractory component and low temperatures for the volatile component, supporting the hypothesis of Grossman and Wasson (1983) that the alkalies condensed on the alumina already available.

Weisberg, Michael K.↗
NASA NTRS1989

Glass Coats For Hot Isostatic Pressing

Surface voids sealed from pressurizing gas. Coating technique enables healing of surface defects by hot isostatic pressing (HIP). Internal pores readily closed by HIP, but surface voids like cracks and pores in contact with pressurizing gas not healed. Applied to casting or weldment as thick slurry of two glass powders: one melts at temperature slightly lower than used for HIP, and another melts at higher temperature. For example, powder is glass of 75 percent SiO2 and 25 percent Na2O, while other powder SiO2. Liquid component of slurry fugitive organic binder; for example, mixture of cellulose acetate and acetone. Easy to apply, separates voids from surrounding gas, would not react with metal part under treatment, and easy to remove after pressing.

Ecer, Gunes M.↗
NASA NTRS1985

Ceramic oxide reactions with V2O5 and SO3

Ceramic oxides are not inert in combustion environments, but can react with, inter alia, SO3, and Na2SO4 to yield low melting mixed sulfate eutectics, and with vanadium compounds to produce vanadates. Assuming ceramic degradation to become severe only when molten phases are generated in the surface salt (as found for metallic hot corrosion), the reactivity of ceramic oxides can be quantified by determining the SO3 partial pressure necessary for molten mixed sulfate formation with Na2SO3. Vanadium pentoxide is an acidic oxide that reacts with Na2O, SO3, and the different ceramic oxides in a series of Lux-Flood type of acid-base displacement reactions. To elucidate the various possible vanadium compound-ceramic oxide interactions, a study was made of the reactions of a matrix involving, on the one axis, ceramix oxides of increasing acidity, and on the other axis, vanadium compounds of increasing acidity. Resistance to vanadium compound reaction increased as the oxide acidity increased. Oxides more acidic than ZrO2 displaced V2O5. Examination of Y2O3- and CeO2-stabilized ZrO2 sintered ceramics which were degraded in 700 C NaVO3 has shown good agreement with the reactions predicted above, except that the CeO2-ZrO2 ceramic appears to be inexplicably degraded by NaVO3.

Jones, R. L.↗
NASA NTRS1988

Hot corrosion of ceramic engine materials

A number of commercially available SiC and Si3N4 materials were exposed to 1000 C in a high velocity, pressurized burner rig as a simulation of a turbine engine environment. Sodium impurities added to the burner flame resulted in molten Na2SO4 deposition, attack of the SiC and Si4N4 and formation of substantial Na2O-x(SiO2) corrosion product. Room temperature strength of the materials decreased. This was a result of the formation of corrosion pits in SiC, and grain boundary dissolution and pitting in Si3N4. Corrosion regimes for such Si-based ceramics have been predicted using thermodynamics and verified in rig tests of SiO2 coupons. Protective mullite coatings are being investigated as a solution to the corrosion problem for SiC and Si3N4. Limited corrosion occurred to cordierite (Mg2Al4Si5O18) but some cracking of the substrate occurred.

Fox, Dennis S.↗
NASA NTRS1988

Pan-African alkali granites and syenites of Kerala as imprints of taphrogenic magmatism in the South Indian shield

Granite and syenite plutons with alkaline affinities ranging in age from 550 to 750 Ma sporadically puncture the Precambrian granulites of the Kerala region. All the bodies are small (20 to 60 sq km), E-W to NW-SE elongated elliptical intrusives with sharp contacts and lie on or close to major late Proterozoic lineaments. Geochemical plots of A-F-M and An-Ab-Or relations show an apparent alkali enrichment trend on the former, but the plutons define relatively distinct fields on the latter. Most of the plutons are adamellitic to granitic by chemistry. The variations of SiO2 with log sub 10 K2O/MgO (1) brings out the distinct alkaline nature of the plutons. Some of the granites are extremely potassic, like the Peralimala pluton, which shows up to 11.8 percent K2O. On a SiO2-Al2O3-Na2O+K2O (mol percent) plot, the plutons vary from peraluminous to peralkaline, but none are nepheline normative. Low MgO, low to moderate CaO and high Fe2O3/FeO values are other common characteristics. Among trace elements, depletion of Ba, Sr and Rb with high K/Ba and K/Rb values are typical. Overall, the plutons show a trend of decreasing K/Rb ratio with increasing K content. Individual plutons show more clearly defined trends similar to those from granitic masses characterized by plagioclase fractionation.

Santosh, M.↗
NASA NTRS1989

Sodium sulfate - Deposition and dissolution of silica

The hot-corrosion process for SiO2-protected materials involves deposition of Na2SO4 and dissolution of the protective SiO2 scale. Dew points for Na2SO4 deposition are calculated as a function of pressure, sodium content, and sulfur content. Expected dissolution regimes for SiO2 are calculated as a function of Na2SO4 basicity. Controlled-condition burner-rig tests on quartz verify some of these predicted dissolution regimes. The basicity of Na2SO4 is not always a simple function of P(SO3). Electrochemical measurements of an (Na2O) show that carbon creates basic conditions in Na2SO4, which explains the extensive corrosion of SiO2-protected materials containing carbon, such as SiC.

Jacobson, Nathan S.↗
NASA NTRS1989

Volatile fractionation and tektite source material

The arguments used by Love and Woronow (1988) to assess the role played in the origin of bediasites by extensive volatile fractionation are critically examined. Using the ratios of 'refractory' oxides, CaO, Al2O3, and MgO, to the 'volatile' oxides, Na2O and K2O, these authors concluded that vapor fractionation did not play a significant role. In this paper, experimental evidence is presented that shows that the assumption of volatility for the alkali elements (as least with respect to silica) to be not valid under the conditions under which tektites formed. It is shown that the results of vapor fractionation in experiments on glasses of tektite composition are approximately parallel the trends seen in bediasite analysis.

Walter, Louis S.↗
NASA NTRS1990

Burner rig hot corrosion of silicon carbide and silicon nitride

A number of commercially available SiC and Si3N4 materials were exposed to 1000 C for 40 h in a high-velocity, pressurized burner rig as a simulation of an aircraft turbine environment. Na impurities (2 ppm) added to the burner flame resulted in molten Na2SO4 deposition, attack of the SiC and Si3N4, and formation of substantial Na2O+x(SiO2) corrosion product. Room-temperature strength of the materials decreased as a result of the formation of corrosion pits in SiC and grain-boundary dissolution and pitting in Si3N4.

Fox, Dennis S.↗