Engineering Papers⌕ Search

SEARCH · Engineering Papers

Results for “olivines”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 433 records · Page 24

Anhydrous Primary Minerals in Ryugu, Ivuna, and Bennu

Samples returned from asteroid Ryugu are chemically and mineralogically similar to CI chondrites [e.g., 1–3]. Both are predominantly composed of low-temperature aqueously formed secondary minerals, whereas high-temperature anhydrous primary minerals, such as olivine, low-Ca pyroxene, spinel, and hibonite, are rarely present. Using secondary ion mass spectrometry (SIMS; Cameca ims-1280HR at Hokkaido University), we performed O [4] and Al–Mg [5] isotope measurements of anhydrous primary minerals in samples of Ryugu and the Ivuna CI chondrite to constrain their origin.Anhydrous primary minerals in our samples of Ryugu and Ivuna occur mostly as monomineralic isolated grains embedded in hydrated matrix. Their O-isotope compositions are distributed along the slope-1 line on the O three-isotope diagram and range from Δ17O ~ –23 to 0‰. Mg-Al spinel grains are 16O-rich (Δ17O ~ –23‰). Low-Ca pyroxene grains are 16O-poor (Δ17O ~ –5‰). Olivine grains show a bimodal distribution of O-isotope composition:10 of 34 grains measured are 16O-rich (Δ17O ~ –23‰) and 24 grains are 16O-poor (Δ17O ~ –7 to 0‰). We found refractory inclusions composed of Mg-Al spinel and hibonite, one from Ryugu and one from Ivuna. Also, in Ivuna, we found an amoeboid olivine aggregate ( AOA) composed of olivine, diopside, anorthite, and Mg-Al spinel and an inclusion composed of olivine and Mg-Al spinel. The minerals in all of these inclusions are 16O-rich (Δ17O ~ –24‰).The 16O-rich grains and inclusions are mineralogically and O-isotopically similar to calcium-aluminum–rich inclusions (CAIs) and AOAs reported in other carbonaceous chondrites [6, 7]. In addition, the initial 26Al/27Al ratios of the two spinel-hibonite inclusions are inferred as ~4.4 × 10–5, also similar to most CAIs in carbonaceous chondrites [6, 8]. The range of Δ17O values for the 16O-poor olivine and low-Ca pyroxene grains is consistent withthat of these minerals in chondrules in most carbonaceous chondrites [9]. Moreover, the most frequent Δ17O value (–6‰) for Mg-rich (Mg# > 97) olivine grains is identical to those for chondrules. Although CI chondrites and Ryugu samples are devoid of chondrules, the 16O-poor grains most likely represent fragments of chondrule-like objects. The presence of both 16O-poor chondrule-like and 16O-rich refractory inclusion–like minerals in Ryugu and Ivuna suggests that some of their building blocks are similar to those of other carbonaceous chondrite groups. They both probably formed in the inner solar protoplanetary disk and were subsequently transported outward.Preliminary data for petrography of asteroid Bennu samples and chemical and isotopic compositions of theiranhydrous primary minerals will also be presented in the meeting.

N Kawasaki↗

Mineral chemistry of the shergottites, nakhlites, Chassigny, Brachina, pallasites and urelites

The mineral chemistry is compared for selected achondrites. Olivine in the ALHA 77005 and EETA 79001 shergottites, olivine-rich Chassigny and Brachina, and the nakhlites, contains Ni indicative of oxidizing conditions, whereas pallasitic and ureilitic olivines contain much lower Ni due to reducing conditions. The Brachina olivine and pyroxene have distinctively higher Fe/Mn than the shergottites and Chassigny, further indicating that Brachina is unique. The Chassigny and 77005 olivines contain lower Cr2O3 (0.03 wt. pct) than the Brachina and 79001 olivines. Values of Fe/Mn for cumulus augites in nakhlites are higher than for the shergottites, whereas those for ferropigeonites are not. The 77005 shergottite contains troilite FeS in contrast to 79001, Shergotty, Zagami, and Chassigny, which contain pyrrhotite. Further analyses are needed, but the present survey indicates that at least Brachina is not chemically cogenetic with the other 'oxidized achondrites', and that the Fe/Mn ratio of the cumulus augites in nakhlites is a problem for the assignment of the nakhlites, shergottites, and Chassigny to a single genetic group.

Smith, J. V.↗

Evidence for relict grains in chondrules of Qingzhen, an E3 type enstatite chondrite

Petrographic and chemical studies of the Qingzhen chondrite strongly suggest that it is the most highly unequilibrated (type 3) enstatite chondrite recognized so far. Qingzhen contains abundant, well-defined chondrules, some of which were incompletely molten during the chondrule formation process. The relict olivine grains within these chondrules contain dusty inclusions of almost pure metallic Fe, which appear to be the in situ reduction product of the fayalitic component of the olivine. The reduction process presumably took place at the time of chondrule formation and the chondrule precursor material must have been more oxidized than average enstatilite chondrite material. It is believed that this oxidized material may have formed at the enstatite chondrite formation location in the solar nebula, provided fluctuations in the degree of oxidation of the nebular gas existed at such locations. Reheating of this material under more reducing conditions would lead to the observed reduction of the olivine. Igneous olivines within chondrules always contain detectable amounts of CaO, while relict olivines are essentially CaO-free. This seems to suggest thatg the relict olivines did not originate during a previous igenous process of chondrule formation and might represent condensation products from the early solar nebula.

Rambaldi, E. R.↗

High-pressure experiments on magnesian eucrite compositions - Constraints on magmatic processes in the eucrite parent body

Melting experiments were conducted on synthetic analogs of two magnesian eucrite clasts from howardites, Kapoeta clast rho and Yamato 7308 pigeonite-eucrite clast 1, at 1 atm and 1-kbar pressure at oxygen fugacities in the range of iron-wuestite (IW) to iron-quartz-fayalite (IQF). The compositions of liquids and coexisting minerals (olivine-low-Ca pyroxene-plagioclase spinel) were used to constrain possible melting and crystallization processes in the parent bodies of eucrite basalts. In agreement with previous studies, the experimental results at 1 atm indicate that the olivine-low-Ca pyroxene-plagioclase-spinel-liquid and olivine-low Ca pyroxene-spinel-liquid boundaries are reaction boundaries involving olivine. At 1 kbar, however, the olivine primary-phase volume shrinks, and the reaction relationship involving olivine disappears for both boundaries. The maximum pressure attained in a Vesta-sized eucrite parent body (EPB) is about 1 kbar, and these results provide important constraints on models relating the howardite-eucrite-diogenite (HED) meteorite association through melting and differentiation processes.

Bartels, K. S.↗

More on the cooling history of angrite LEW 86010

Antarctic angrite LEW 86010 has many chemical and mineralogical characteristics which suggest it is closely related to Angra dos Reis (ADOR). However, these meteorites have had very different thermal histories. Olivines and pyroxenes in ADOR are nearly homogeneous, suggesting very slow cooling or extensive subsolidus equilibration. In contrast, LEW 86010 pyroxenes are extensively zoned in both major and trace elements, while olivines are nearly homogeneous, suggesting that cooling of this sample was slow enough to homogenize olivines, but too fast to homogenize pyroxenes. In an earlier study, we used Ca diffusion gradients associated with exsolution lamellae of kirsh-steinite in LEW 86010 olivines to estimate the cooling rate of this sample. We obtained cooling rates of a few x.01 deg C/yr, corresponding to a burial depth of approximately 10(exp 2) m under solid rock (thermal diffusivity = 0.004 sq cm/s), or approximately m under regolith material (10(exp -5) sq cm/s). Unfortunately, this calculation was very sensitive to the assumed temperature of initial exsolution, which we approximated from the estimated initial olivine bulk Ca content, and also to the extrapolated values for the Ca diffusion coefficient (D sub Ca). This abstract reports new cooling rate estimates obtained using a refined approach that includes the initial temperature of exsolution as one of the fitted parameters. The purpose of our new calculations is (1) to reduce uncertainties in cooling rate due to uncertainties in bulk olivine Ca content and initial exsolution temperature, (2) to investigate the effects of using different values for D sub Ca, and (3) to determine how well constrained the cooling rate is for any particular Ca diffusion coefficient.

Mckay, G.↗

Rb-Sr and Sm-Nd Isotopic Studies of Shergottite Y980459 and a Petrogenetic Link Between Depleted Shergottites and Nakhlites

Y980459 was found near the Minami-Yamato Nunataks, Antarctica in 1998 and was recently classified as an olivine-bearing shergottite. It petrographically resembles many other olivine-phyric shergottites mostly found in hot deserts, e.g. DaG476/489, SaU005/094, Dohfar 019, NWA 1068/1110, NWA 1195 and EETA 79001 lith.A. However, Y980459 is unique among these meteorites in several respects. It is apparently very fresh and only weakly shocked. Also, it completely lacks plagioclase, but contains abundant residual volcanic glass. This group of olivine-phyric shergottites is characterized by variable crystallization ages from approx.172 Ma to approx.575 Ma and ejection ages from approx.1 Ma to approx.20 Ma. They probably represent volcanic melts originated from the deep Martian mantle. We performed Rb-Sr and Sm-Nd isotopic analyses on Y980459 to determine its crystallization age and compared its age and isotopic signatures with those obtained from other olivine-phyric shergottites and QUE 94201, the other Antarctic olivine-free shergottite. QUE 94201 and some olivine-phyric shergottites e.g. DaG, SaU, Doh and EETA lith A have similar depleted-LREE patterns and are herein referred to as depleted shergottites. A petrogenetic model correlating depleted shergottites and nakhlites is also proposed. Preliminary Rb-Sr and Sm-Nd isotopic data for Y980459 were presented earlier at the NIPR, Japan, in 2003.

Shih, C.-Y.↗

Petrology and Geochemistry of New Ureilites and Ureilite Genesis

Ureilites are C-bearing, basalt-depleted olivine+pyroxene achondrites from a differentiated asteroid. The group is heterogeneous, exhibiting ranges in O isotopic composition, Fe/Mg, Fe/Mn, pyx/ol, siderophile and lithophile trace element content, and C content and isotopic composition [1]. Some of these characteristics are nebular in origin; others were strongly overprinted by asteroidal igneous processes. The consensus view is that most ureilites are melt-residues, but some are partial cumulates or have interacted with a melt [1,2]. An "unroofing" event occurred while the parent asteroid was hot that froze in mineral core com-positions and resulted in FeO reduction at olivine grain margins. We have studied several new ureilites, but will focus here on two anomalous stones; LAR 04315 and NWA 1241. LAR 04315 is texturally unusual. It contains olivine with angular subdomains, and low-Ca pyroxene riddled with wormy inclusions of metal+troilite, graphite, and possibly other phases, and irregular inclusions of high-Ca pyroxene. Reduction occurred along olivine grain margins and internal fractures, but not along subdomain boundaries. Although texturally odd, LAR 04351 is a typical ureilite in mineral and bulk composition. The olivine is Fo80.8 and falls on the ureilite Fe/Mn-Fe/Mg trend. Its olivine composition falls within the range of the majority of ureilites, and it is typical of these ureilites in bulk rock lithophile and siderophile element contents.

Mittlefehldt, David W.↗

Experimental Constraints on Ureilite Petrogenesis

This experimental study explores the petrogenesis of ureilites by a partial melting/smelting process. Experiments have been performed over temperature (1150-1280 C), pressure (5-12.5 MPa), and low oxygen fugacity (graphite-CO gas) conditions appropriate for a hypothetical ureilite parent body approximately 200 km in size. Experimental and modeling results indicate that a partial melting/smelting model of ureilite petrogenesis can explain many of the unique characteristics displayed by this meteorite group. Compositional information preserved in the pigeonite-olivine ureilites was used to estimate the composition of melts in equilibrium with the ureilites. The results of 20 experiments saturated with olivine, pyroxene, metal, and liquid with appropriate ureilite compositions are used to calibrate the phase coefficients and pressure-temperature dependence of the smelting reaction. The calibrated coefficients are used to model the behavior of a hypothetical residue that is experiencing fractional smelting. The residue is initially olivine-rich and smelting progressively depletes the olivine content and enriches the pyroxene and metal contents of the residues. The modeled residue composition at 1260 C best reproduces the trend of ureilite bulk compositions. The model results also indicate that as a ureilite residue undergoes isothermal decompression smelting over a range of temperatures, Ca/Al values and Cr203 contents are enriched at lower temperatures (below about 1240 C) and tend to decrease at higher temperatures. Therefore, fractional smelting can account for the high Ca/A1 and Cr203 wt% values observed in ureilites. We propose that ureilites were generated from an olivine-rich, cpx-bearing residue. Smelting began when the residue was partially melted and contained liquid, olivine, and carbon. These residues experienced varying degrees of fractional smelting to produce the compositional variability observed within the pigeonite-bearing ureilites. Variations in mineral composition, modal proportions, and isotopic signatures are best described by heterogeneous accretion of the ureilite parent body followed by minimal and variable degrees of igneous processing.

Singletary, Steven↗

An Experimental Investigation of the Shergottite NWA 6162

The Martian meteorite North West Africa 6162 (NWA 6162) is a shergottite found in Morocco in 2010. The meteorite has large olivine crystals with Mg-depleted rims as low as FO(sub 65) and Mg-rich cores of up to FO(sub 74). It is similar both in appearance and composition to another shergottite, SaU 005. Our objective is to determine if NWA 6162 represents a liquid or if it is a product of olivine accumulation. Olivine accumulation would leave the parent melt Mg-depleted and the complementary olivine cumulates would be Mg-enriched. Therefore, if NWA 6162 is a partial cumulate we would expect that liquidus olivines grown from this bulk composition would be more magnesium than olivines in the natural sample.

Barnett, R. Gaylen↗

The Role of Water in the Stability of Cratonic Keels

Cratons are typically underlain by large, deep, and old lithospheric keels (to greater than 200 km depth, greater than 2.5 Ga old) projecting into the asthenosphere (e.g., Jordan, 1978; Richardson et al., 1984). This has mystified Earth scientists as the dynamic and relatively hot asthenosphere should have eroded away these keels over time (e.g., Sleep, 2003; O'Neill et al., 2008; Karato, 2010). Three key factors have been invoked to explain cratonic root survival: 1) Low density makes the cratonic mantle buoyant (e.g., Poudjom Djomani et al., 2001). 2) Low temperatures (e.g., Pollack, 1986; Boyd, 1987), and 3) low water contents (e.g., Pollack, 1986), would make cratonic roots mechanically strong. Here we address the mechanism of the longevity of continental mantle lithosphere by focusing on the water parameter. Although nominally anhydrous , olivine, pyroxene and garnet can accommodate trace amounts of water in the form of H bonded to structural O in mineral defects (e.g., Bell and Rossman, 1992). Olivine softens by orders of magnitude if water (1-1000 ppm H2O) is added to its structure (e.g., Mackwell et al., 1985). Our recent work has placed constraints on the distribution of water measured in peridotite minerals in the cratonic root beneath the Kaapvaal in southern Africa (Peslier et al., 2010). At P greater than 5 GPa, the water contents of pyroxene remain relatively constant while those of olivine systematically decrease from 50 to less than 10 ppm H2O at 6.4 GPa. We hypothesized that at P greater than 6.4 GPa, i.e. at the bottom of the cratonic lithosphere, olivines are essentially dry (greater than 10 ppm H2O). As olivine likely controls the rheology of the mantle, we calculated that the dry olivines could be responsible for a contrast in viscosity between cratonic lithosphere and surrounding asthenosphere large enough to explain the resistance of cratonic root to asthenospheric delamination.

Peslier, Anne H.↗

Experimental Constraints on a Vesta Magma Ocean

A magma ocean model was devised to relate eucrites (basalts) and diogenites (orthopyroxenites), which are found mixed together as clasts in a suite of polymict breccias known as howardites. The intimate association of eucritic and diogenitic clasts in howardites argues strongly that these three classes of achondritic meteorites all originated from the same planetoid. Reflectance spectral evidence (including that from the DAWN mission) has long suggested that Vesta is indeed the Eucrite Parent Body. Specifically, the magma ocean model was generated as follows: (i) the bulk Vesta composition was taken to be 0.3 CV chondrite + 0.7 L chondrite but using only 10% of the Na2O from this mixture; (ii) this composition is allowed to crystallize at 500 bar until approx. 80% of the system is solid olivine + low-Ca pyroxene; (iii) the remaining 20% liquid crystallizes at one bar from 1250C to 1110C, a temperature slightly above the eucrite solidus. All crystallization calculations were performed using MELTS. In this model, diogenites are produced by cocrystallization of olivine and pyroxene in the >1250C temperature regime, with Main Group eucrite liquids being generated in the 1300-1250C temperature interval. Low-Ca pyroxene reappears at 1210C in the one-bar calculations and fractionates the residual liquid to produce evolved eucrite compositions (Stannern Trend). We have attempted to experimentally reproduce the <1250C portion of the MELTS Vesta magma ocean. In the MELTS calculation, the change from 500 bar to one bar results in a shift of the olivine:low-Ca pyroxene boundary so that the 1250C liquid is now in the olivine field and, consequently, olivine should be the first-crystallizing phase, followed by low-Ca pyroxene at 1210C, and plagioclase at 1170C. Because at one bar the olivine:low-Ca pyroxene boundary is a peritectic, fractional crystallization of the 1210C liquid proceeds with only pyroxene crystallization until plagioclase appears. Thus, the predictions of the MELTS calculation are clear and straightforward.

Hoff, C.↗

Water in the Cratonic Mantle: Insights from FTIR Data on Lac De Gras Xenoliths (Slave Craton, Canada)

The mantle lithosphere beneath the cratonic part of continents is the deepest (> 200 km) and oldest (>2-3 Ga) on Earth, remaining a conundrum as to how these cratonic roots could have resisted delamination by asthenospheric convection over time. Water, or trace H incorporated in mineral defects, could be a key player in the evolution of continental lithosphere because it influences melting and rheology of the mantle. Mantle xenoliths from the Lac de Gras kimberlite in the Slave craton were analyzed by FTIR. The cratonic mantle beneath Lac de Gras is stratified with shallow (<145 km) oxidized ultradepleted peridotites and pyroxenites with evidence for carbonatitic metasomatism, underlain by reduced and less depleted peridotites metasomatized by kimberlite melts. Peridotites analyzed so far have H O contents in ppm weight of 7-100 in their olivines, 58 to 255 in their orthopyroxenes (opx), 11 to 84 in their garnet, and 139 in one clinopyroxene. A pyroxenite contains 58 ppm H2O in opx and 5 ppm H2O in its olivine and garnet. Olivine and garnet from the deep peridotites have a range of water contents extending to higher values than those from the shallow ones. The FTIR spectra of olivines from the shallow samples have more prominent Group II OH bands compared to the olivines from the deep samples, consistent with a more oxidized mantle environment. The range of olivine water content is similar to that observed in Kaapvaal craton peridotites at the same depths (129-184 km) but does not extend to as high values as those from Udachnaya (Siberian craton). The Slave, Kaapvaal and Siberian cratons will be compared in terms of water content distribution, controls and role in cratonic root longevity.

Peslier, Anne H.↗

Melt Inclusion Analysis of RBT 04262 with Relationship to Shergottites and Mars Surface Compositions

Martian meteorite RBT 04262 is in the shergottite class. It displays the two lithologies typically found in "lherzolitic shergottites": one with a poikilitic texture of large pyroxene enclosing olivine and another with non-poikilitic texture. In the case of RBT 04262, the latter strongly ressembles an olivine- phyric shergottite which led the initial classification of this meteorite in that class. RBT 04262 has been studied with regards to its petrology, geochemistry and cosmic ray exposure and belongs to the enriched oxidized end-member of the shergottites. Studies on RBT 04262 have primarily focused on the bulk rock composition or each of the lithologies independently. To further elucidate RBT 04262's petrology and use it to better understand Martian geologic history, an in-depth study of its melt inclusions (MI) is being conducted. The MI chosen for this study are found within olivine grains. MI are thought to be trapped melts of the crystallizing magma preserved by the encapsulating olivine and offer snapshots of the composition of the magma as it evolves. Some MI, in the most Mg-rich part of the olivine of olivine-pyric shergottites, may even be representative of the meteorite parent melt.

Potter, S. A.↗

Understanding the Space Weathering of Mercury Through Laboratory Experiments

Introduction: Airless surfaces across the solar system are continually modified by energetic particles from solar wind and micrometeoroid bombardment [1,2]. This process is known as space weathering, and it alters the chemical, microstructural, and optical properties of surface regoliths on airless bodies, including Mercury. On the Moon and S-type asteroids, the reflectance spectral signatures of space weathering include reddening (increasing reflectance with increasing wavelength), darkening (lowering of reflectance), and the attenuation of characteristic absorption bands [2]. Such spectral changes are driven by the production of Fe-bearing nanoparticles(npFe) through both solar wind irradiation and micrometeoroid bombardment. While our understanding of space weathering for the Moon and near-Earth S-types asteroids is advanced, insight into how these processes operate on other planetary bodies is limited. In particular, Mercury experiences a uniquely intense space weathering environment than planetary counterparts at 1 AU, including a moreintense solar wind flux and higher velocity micrometeoroid impacts [4]. Additionally, Mercury has a surface composition unique in the inner solar system, including regions of the surface with very low albedo known as the low reflectance material (LRM), which is enriched in carbon, likely graphite, up to 4wt.% [5].In addition, the concentration of Fe across Mercury’s surface islow (<2 wt.%) compared to the Moonor S-type asteroids asteroids[6]. Our understanding of the effects of space weathering on C-rich and Fe-poor phases is limited. Since Fe plays a critical role inthe development of space weathering characteristicson other airless surfaces(e.g., npFe), its limited availability may significantly affect the development of space weathering features in Mercury surface materials. We can simulate space weathering processes in the laboratory to explore their effects on the microstructural, chemical, and spectral characteristics of Mercury surface materials[7]. Here we used pulsed laser irradiation to simulate the short duration, high-temperature events associated with micrometeoroid impacts. We performed coordinated analyses including reflectance spectroscopy and electron microscopy to investigate the spectral, chemical, and microstructural changes in these mercurian analog samples. Methods: For these experiments, we usedforsteritic olivine with varying FeOcontents, a mineral phase proposed to be abundant on the surface of Mercury. We mixed each sample with graphite to simulate LRM regions of the surface. Wesynthesized the olivinesamplesat 1-bar at NASA’s Johnson Space Centerand prepared pressed powder pellets for laser irradiation [8].We prepared three samples, each with a base layer of olivineto maintain structural integrity and topped witha surface layer containing the graphite-olivine mixture: 1) Sample SC-001 San Carlos olivine(Fo90.91),2)Sample F-S-002 with0.05 wt.% FeO olivine, and 3) F-T-004 with 0.53 wt.% FeO olivine. Each sample was mixed with 5 wt.% powdered graphite and had grain sizes ranging from 45to 125μm. We irradiated each sample usinga pulsed Nd-YAG laser, (l=1064 nm, ~6 ns pulse duration, energy of 48 mJ/pulse) while undervacuumat Northern Arizona University. The laser was rastered1x and then 5x over the surfaceof each sample to simulate progressive space weathering. We collected in situreflectance spectra from the samples after each laser pulse witha Nicolet IS50 Fourier-Transform Infrared spectrometer (lfrom 0.65-2.5 μm). We used an FEI Nova NanoSEM200scanning electron microscope (SEM) and a Hitachi TM4000 Plus benchtop SEM at Purdue University to image the surface morphology and topography of the samples. We extracted thin sections for analysis in the transmission electron microscope(TEM)using the FEI Helios NanoLab 660 focused ion beam (FIB) SEM at the University of Arizona.We performed analysis of the microstructural and chemical characteristics of the samples using the 200 keV JEOL 2500 scanning TEM at Johnson Space Center. Reflectance Spectroscopy Results:Reflectance spectra for each sample are shown in Fig. 1.SC-001:The spectrum of the unirradiated sample exhibits a weak 1.0 μm absorption feature, associated with Fe2+in the olivine,and low overall reflectance (Fig. 1a). Thereflectance and the depth of the absorption band increases after 1x laser raster but are at their lowest after 5x laser rasters.F-T-004:The unirradiated sample has a blue-sloped spectrum with low reflectance without identifiable absorption features (Fig. 1b). With progressive laser irradiation, the sample reflectance increases and becomes strongly red-sloped.F-S-002:The unirradiated sample exhibits a dark, blue-slopedspectrum. The brightness of the sample increases significantly from <0.2average reflectance over >0.8 reflectance in the most irradiated sampleand thespectral slope also becomesslightly reddened (Fig. 1c). Microstructural and Chemical Analysis: Two primary alteration textures were observed in the samples exposed to simulated space weathering: 1) fluffy C-rich,and 2) vesiculated melt. The fluffy C-rich texture is composed oflow-densitydeposits distributed across the surface of the sample(Fig. 2A). Analysis of a FIB section extracted from a low-density C-rich region in sample SC-001 reveals multiple globule-type deposits, discrete from stacked graphite, likely produced via melting from the laser irradiation [9].The vesiculated melt textureis smooth and uniformly distributed across isolated regions of the sample surface. The vesicles measure up to 100s of nmin diameter. Analysis of a FIB section from this texture was extracted from sample F-T-004 reveals a layer of amorphous melt material, close to 100 nm thick and uniform across the FIB section (Fig. 2B). Isolated regions of this melt layer contain small nanoparticles, <5 nm in diameter. Chemical analysis through energy dispersive X-ray spectroscopy reveals the composition of this layer is enriched in Si and depleted in Mg and O compared to the underlying sample. Implications for Space Weathering on Mercury: Previous experiments simulating space weathering of Mercury have showndarkening and reddening of spectra[7,10].However, our use of low-Fe materials and graphite to create a sample set more analogous to the mercurian surface. Our results indicate that sample composition plays a significant and important role in the space weathering of Mercury. In particular, our spectral data demonstrates a strong correlation between spectral slope, Fe content, and simulated space weathering. While the variation in FeO content between samples F-S-002 and F-T-004 is <0.6 wt.%, the spectra deviate from flat to strongly red-sloped(F-T-004). This reddeningmay be linked to the presence of very small nanoparticles observed in the melt textures extracted from sample F-T-004. For the SC-001 sample, the fluffy C-rich textures may be developed by the amalgamation of small graphite particles into these unique morphologies. Such observations indicate that space weathering on Mercury may result in both familiar and new microstructural and chemical characteristics. References: [1]Hapke B. (2001) J. Geophys. Res.-Planet.,106,10039–10073. [2]Pieters C.M. and Noble S.K. (2016) J. Geophys. Res-Planet., 121, 1865–1884. [3] Lucey P.G., and Riner, M.A. (2011) Icarus,212, 451-462.[4]CintalaM.J.(1992)J. Geophys. Res.-Planet.,97,947–973.[5]Klima R.L.et al.(2018)Geophys.Res.Letters, 45, 2945–2953. [6]Nittler L.R., et al. (2011) Science 333, 1847-1850.[7]Sasaki S. and Kurahashi E. (2004) Space weathering on Mercury, Adv.Space Res., 33, 2152-2155.[8] Vander KaadenK.E., et al. (2018) LPSCXLIX, Abstract 1230. [9] McGlaun M.L. et al. (2019) LPSCL, Abstract 2019. [10] TrangD.et al. (2018)LPSCXLIX,Abstract2083

M S Thompson↗

Stabilizing the crystal structures of NaFePO 4 with Li substitutions

Due to the high cost and insufficient resources of lithium, alternative sodium-ion batteries have been widely investigated for large-scale applications. NaFePO 4 has the highest theoretical capacity of 154 mA h g -1 among the iron-based phosphates, which makes it an attractive cathode material for Na-ion batteries. Experimentally, LiFePO 4 has been highly successful as a cathode material in Li-ion batteries because its olivine crystal structure provides a stable framework during battery cycling. In NaFePO 4 , maricite replaces olivine as the most stable phase. However, the maricite phase is experimentally found to be electrochemically inactive under normal battery operating voltages (0–4.5 V). We found that partial substitutions of Na with Li stabilize the olivine structure and may be a way to improve the performance of NaFePO 4 cathodes. Using the previously developed structural LiFePO 4 database, here we examine the low-energy crystal structures in the system when we replace Li with Na. The known maricite and olivine NaFePO 4 phases are reconfirmed and an unreported phase with energy between them is identified by our calculations. Besides, the Li-doped olivine type compound Li x Na 1- x FePO 4 with mixed alkali ions retains better energetic stability compared with the other two types of structures of the same composition, as long as the proportion of Li exceeds 0.25. The thermodynamic stability of o-type Li x Na 1- x FePO 4 can be further improved at finite temperatures. The primary limitation of the calculations is that we mainly focus on the zero-temperature condition; however, the relative stability of the structures may vary depending on the ambient temperature.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Differentiation of an Apollo 12 picrite magma

The Apollo 12 olivine basalt suite shows a strong positive correlation of grain size with normative olivine content. This correlation is interpreted to mean that the suite of samples represents the basal portion of a cooling unit which differentiated by simple olivine settling. The grain size of plagioclase observed in the coarsest samples indicates the cooling unit may have been as much as 30 m thick. The amount of olivine concentration observed in the suite is quantitatively internally consistent with simple olivine settling in a magma body of this size which has the composition of the chill margin.

Walker, D.↗

Chemistry of Apollo 12 mare basalts - Magma types and fractionation processes

Major and trace element data for a large suite of petrographically diverse Apollo 12 mare basalts are presented, and magma types sampled at the Apollo 12 site are characterized. The data confirm earlier classifications of the basalts into olivine, pigeonite, ilmenite, and feldspathic basalts. The olivine and pigeonite basalts are shown to be comagnetic and related by olivine fractionation. The other types, which differ in trace element and isotopic characteristics, are derived from different sources within the lunar interior. The spatial relations between the main basalt types are discussed in terms of local cratering events, and it is suggested that the younger ilmenite basalts overlie the olivine-pigeonite basalts. The role of olivine-dominated near-surface crystal fractionation in causing chemical variation is examined, and a relation between inferred cooling rate and the position of a sample in the fractionation sequence is determined.

Rhodes, J. M.↗

Petrology of crystalline matrix breccias from Apollo 17 rake samples

The petrology, mineralogy, and composition of 13 crystalline matrix breccias from the Apollo 17 rake samples are described. The breccias have matrices of uniform modal mineralogy (plagioclase, 50-54%; olivine and pyroxene, 41-46%) but diverse textures. Clast characteristics, including the proportion of plagioclase, the composition in comparison with matrix, and the textures of different clast types, are reported. The majority of bulk matrix compositions plot on or very near the plagioclase-olivine cotectic in the system olivine-anorthite-silica. If the matrix compositions represent impact total melts, the inferred cotectic control requires that the source material was itself an igneous differentiate with compositions along the plagioclase-olivine cotectic. Alternatively, the proximity of the matrix compositions to the plagioclase-olivine cotectic could be accounted for if the breccia matrices represent a suite of impact-generated partial melts.

Warner, R. D.↗