Implications of spinel compositions for the petrotectonic history of abyssal peridotite from Southwest Indian Ridge (SWIR)

Science.gov (United States)

Chen, T.; Jin, Z.; Wang, Y.; Tao, C.

2012-12-01

Abyssal peridotites generate at mid-ocean ridges. Lherzolite and harzburgite are the main rock types of peridotites in the uppermost mantle. The lherzolite subtype, less depleted and less common in ophiolites, characterizes mantle diapirs and slow-spreading ridges. Along the Earth's mid-ocean ridges, abyssal peridotites undergo hydration reactions to become serpentinite minerals, especially in slow to ultraslow spreading mid-ocean ridges. Spinel is common in small quantities in peridotites, and its compositions have often been used as petrogenetic indicators [1]. The Southwest Indian Ridge (SWIR) is one of the two ultraslow spreading ridges in the world. The studied serpentinized peridotite sample was collected by the 21st Voyage of the Chinese oceanic research ship Dayang Yihao (aka Ocean No. 1) from a hydrothermal field (63.5°E, 28.0°S, and 3660 m deep) in SWIR. The studied spinels in serpentinized lherzolite have four zones with different compositions: relic, unaltered core is magmatic Al-spinels; micro- to nano- sized ferrichromite zoned particles; narrow and discontinuous magnetite rim; and chlorite aureoles. The values Cr# of the primary Al-spinels indicate the range of melting for abyssal peridotites from SWIR extends from ~4% to ~7% [2]. The alteration rims of ferrichromite have a chemical composition characterized by Fe enrichment and Cr# increase indicating chromite altered under greenschist-amphibolite facies. Magnetites formed in syn- and post- serpentinization. Chlorite (clinochlore) formed at the boundary and crack of spinel indicating it had undergone with low-temperature MgO- and SiO2-rich hydrothermal fluids [3]. It suggests that serpentinized lherzolite from SWIR had undergone poly-stage hydration reactions with a wide range of temperature. Acknowledgments: EMPA experiment was carried out by Xihao Zhu and Shu Zheng in The Second Institute of Oceanography and China University of Geosciences, respectively. The work was supported by NSFC

Lithospheric mantle evolution in the Afro-Arabian domain: Insights from Bir Ali mantle xenoliths (Yemen)

Science.gov (United States)

Sgualdo, P.; Aviado, K.; Beccaluva, L.; Bianchini, G.; Blichert-Toft, J.; Bryce, J. G.; Graham, D. W.; Natali, C.; Siena, F.

2015-05-01

Detailed petrological and geochemical investigations of an extensive sampling of mantle xenoliths from the Neogene-Quaternary Bir Ali diatreme (southern Yemen) indicate that the underlying lithospheric mantle consists predominantly of medium- to fine-grained (often foliated) spinel-peridotites (85-90%) and spinel-pyroxenites (10-15%) showing thermobarometric estimates in the P-T range of 0.9-2.0 GPa and 900-1150 °C. Peridotites, including lherzolites, harzburgites and dunites delineate continuous chemical, modal and mineralogical variations compatible with large extractions of basic melts occurring since the late Proterozoic (~ 2 Ga, according to Lu-Hf model ages). Pyroxenites may represent intrusions of subalkaline basic melts interacting and equilibrated with the host peridotite. Subsequent metasomatism has led to modal changes, with evidence of reaction patches and clinopyroxene and spinel destabilization, as well as formation of new phases (glass, amphibole and feldspar). These changes are accompanied by enrichment of the most incompatible elements and isotopic compositions. 143Nd/144Nd ranges from 0.51419 to 0.51209 (εNd from + 30.3 to - 10.5), 176Hf/177Hf from 0.28459 to 0.28239 (εHf from + 64.4 to - 13.6), and 208Pb/204Pb from 36.85 to 41.56, thus extending from the depleted mantle (DM) towards the enriched OIB mantle (EM and HIMU) components. 3He/4He (R/RA) ratios vary from 7.2 to 7.9 with He concentrations co-varying with the most incompatible element enrichment, in parallel with metasomatic effects. These metasomatic events, particularly effective in harzburgites and dunites, are attributable to the variable interaction with alkaline basic melts related to the general extensional and rifting regime affecting the East Africa-Arabian domain during the Cenozoic. In this respect, Bir Ali mantle xenoliths resemble those occurring along the Arabian margins and the East Africa Rift system, similarly affected by alkaline metasomatism, whereas they are

The first find of spinel peridotite in the Southern Kazakhstan: Structure, composition, and parameters of high-pressure metamorphism

Science.gov (United States)

Pilitsyna, A. V.; Tretyakov, A. A.; Alifirova, T. A.; Degtyarev, K. E.; Kovalchuk, E. V.

2017-09-01

Spinel peridotite, metamorphosed in high-pressure conditions, was first described within the Western part of the Central Asian Orogenic Belt. The spinel peridotite has the characteristics of Mg-Cr ultramafites indicating the mantle origin of its protolith. The preliminary estimation of the metamorphism peak for the model system MgO-Al2O3—SiO2-Cr2O3 (MASCr) is 10-19 kbar at 680-800°C.

Petrochemistry of a xenolith-bearing Neogene alkali olivine basalt from northeastern Iran

Science.gov (United States)

Saadat, Saeed; Stern, Charles R.

2012-05-01

A small isolated Neogene, possibly Quaternary, monogenetic alkali olivine basalt cone in northeastern Iran contains both mantle peridotite and crustal gabbroic xenoliths, as well as plagioclase megacrysts. The basaltic magma rose to the surface along pathways associated with local extension at the junction between the N-S right-lateral and E-W left-lateral strike slip faults that form the northeastern boundary of the Lut microcontinental block. This basalt is enriched in LREE relative to HREE, and has trace-element ratios similar to that of oceanic island basalts (OIB). Its 87Sr/86Sr (0.705013 to 0.705252), 143Nd/144Nd (0.512735 to 0.512738), and Pb isotopic compositions all fall in the field of OIB derived from enriched (EM-2) mantle. It formed by mixing of small melt fractions from both garnet-bearing asthenospheric and spinel-facies lithospheric mantle. Plagioclase (An26-32) megacrysts, up to 4 cm in length, have euhedral crystal faces and show no evidence of reaction with the host basalt. Their trace-element concentrations suggest that these megacrysts are co-genetic with the basalt host, although their 87Sr/86Sr (0.704796) and 143Nd/144Nd (0.512687) ratios are different than this basalt. Round to angular, medium-grained granoblastic meta-igneous gabbroic xenoliths, ranging from ~ 1 to 6 cm in dimension, are derived from the lower continental crust. Spinel-peridotite xenoliths equilibrated in the subcontinental lithosphere at depths of 30 to 60 km and temperatures of 965 °C to 1065 °C. These xenoliths do not preserve evidence of extensive metasomatic enrichment as has been inferred for the mantle below the Damavand volcano further to the west in north-central Iran, and clinopyroxenes separated from two different mantle xenoliths have 87Sr/86Sr (0.704309 and 0.704593) and 143Nd/144Nd (0.512798) ratios which are less radiogenic than either their host alkali basalt or Damavand basalts, implying significant regional variations in the composition and extent of

Sepentinized Peridotite Spinel Composition: Northern Central Indian Ridge at 6°39

Science.gov (United States)

Ray, D.; Banerjee, R.; Iyer, S. D.; Balaram, V.; Speakman, J.

2005-12-01

Exposures of serpentinized peridotites on the seafloor at slow-spreading ridges have been interpreted either as accretion of ridge segments in a magma-starved condition along the non-transform setting or as preferential outcrops at ridge offsets in transform fault setting. Here we present the mineral chemistry and geochemistry of serpentinites and serpentinized spinel peridotites recovered from an off axis region (corner high) at south of Vityaz transform fault (6°39'S), Northern Central Indian Ridge. Our purpose is to use mineral chemical data of serpentine and spinel to investigate the effect of low temperature alteration processes and degree of partial melting. Serpentine composition shows presence of high Mg-rich lizardite and chrysotile pseudomorphs and these rocks mostly preserve `mesh rim', `window' and `hourglass' textures, representing extensive hydration during low temperature hydrothermal alteration. In thin section, serpentine veins (mainly lensoidal, pinch and swell or anastomosing) are common, sometime crosscutting the `mesh rim' textures to attest to the intensity of serpentinization process. In one sample, a 1.9 cm-thick feldspathic vein crosscut the serpentinite as a porphyroblast and this indicates discontinuity in magmatic crust caused due to less magma input at off-axis region facilitate the intrusion of short-living feeder dykes of highly fractionated late magmatic liquids within the peridotite. In addition, in hand specimen, presence of smaller-scale striations analogous to slickenlines on serpentinite surfaces suggests low-angle faulting, which could have enhanced pervasive serpentinization during their subsequent emplacement. Individual serpentine grain displays very low Ca content (0.01 wt%) suggesting possible absence of any secondary Ca-rich phases also verified by very low Sr content (connotation. Limited data on composition of individual spinel porphyroclast exhibits substantial variation in their Mg# (mole [Mg/ Mg+Fe2]) and Cr# (mole

Rheological structure of a lithosphere-asthenosphere boundary zone, decoded from EBSD analysis of mantle xenoliths from Ichinomegata, NE Japan

Science.gov (United States)

Sato, Y.; Ozawa, K.

2017-12-01

Mantle xenoliths are fragments of mantle materials entrapped in alkali basalts or kimberlites and transported to the surface (Nixon, 1987). They provide information on rheological, thermal, chemical, petrological structures of the upper mantle (e.g. Green et al., 2010; McKenzie and Bickle, 1988; O'Reilly and Griffin, 1996). They potentially represent materials from a boundary zone of lithosphere and asthenosphere (LABZ), where the heat transportation mechanism changes from convection to conduction (Sleep, 2005, 2006). However, difficulties in geobarometry for spinel peridotite (e.g. O'Reilly et al., 1997) have hampered our understanding of shallow LABZ. Ichinomegata located in the back-arc side of NE Japan is a latest Pleistocene andesitic-dacitic volcano yielding spinel peridotite xenoliths (Katsui et al., 1979). Through our works (Sato and Ozawa, 2016, 2017a, 2017b), we have overcome difficulties in geobarometry of spinel peridotites and gained accurate thermal structure (0.74-1.60 GPa, 832-1084 °C) from eight of the nine examined xenoliths. The rheological and chemical features suggest drastic changes: undeformed (granular), depleted, subsolidus mantle representing lithospheric mantle (ca. 28-35 km) and deformed (porphyroclastic), fertile, hydrous supersolidus mantle representing rheological LABZ (ca. 35-54 km). We investigate depth dependent variation of crystallographic preferred orientation (CPO) of constituent minerals of the xenoliths by electron back-scattered diffraction analysis (using JSM-7000F with a CCD detector and the CHANNEL5 software at the University of Tokyo). A shallower (ca. 32 km) sample with tabulargranular texture and coarse olivine size (0.92 mm) has A-type olivine CPO with [100] maximum as reported by Satsukawa and Michibayashi (2014) (hereafter SM14), whereas a deep (ca. 51 km) sample with porphyroclastic texture and finer olivine size (0.46 mm) has CPO with weaker fabric intensity characterized by a [100] girdle similar to AG-type and

Mg isotope systematics during magmatic processes: Inter-mineral fractionation in mafic to ultramafic Hawaiian xenoliths

Science.gov (United States)

Stracke, A.; Tipper, E. T.; Klemme, S.; Bizimis, M.

2018-04-01

Observed differences in Mg isotope ratios between bulk magmatic rocks are small, often on a sub per mill level. Inter-mineral differences in the 26Mg/24Mg ratio (expressed as δ26Mg) in plutonic rocks are on a similar scale, and have mostly been attributed to equilibrium isotope fractionation at magmatic temperatures. Here we report Mg isotope data on minerals in spinel peridotite and garnet pyroxenite xenoliths from the rejuvenated stage of volcanism on Oahu and Kauai, Hawaii. The new data are compared to literature data and to theoretical predictions to investigate the processes responsible for inter-mineral Mg isotope fractionation at magmatic temperatures. Theory predicts up to per mill level differences in δ26Mg between olivine and spinel at magmatic temperatures and a general decrease in Δ26Mgolivine-spinel (=δ26Mgolivine - δ26Mgspinel) with increasing temperature, but also with increasing Cr# in spinel. For peridotites with a simple petrogenetic history by melt depletion, where increasing depletion relates to increasing melting temperatures, Δ26Mgolivine-spinel should thus systematically decrease with increasing Cr# in spinel. However, most natural peridotites, including the Hawaiian spinel peridotites investigated in this study, are overprinted by variable extents of melt-rock reaction, which disturb the systematic primary temperature and compositionally related olivine-spinel Mg isotope systematics. Diffusion, subsolidus re-equilibration, or surface alteration may further affect the observed olivine-spinel Mg isotope fractionation in peridotites, making Δ26Mgolivine-spinel in peridotites a difficult-to-apply geothermometer. The available Mg isotope data on clinopyroxene and garnet suggest that this mineral pair is a more promising geothermometer, but its application is restricted to garnet-bearing igneous (garnet pyroxenites) and metamorphic rocks (eclogites). Although the observed δ26Mg variation is on a sub per mill range in bulk magmatic rocks

Compositional trends among Kaapvaal Craton garnet peridotite xenoliths and their effects on seismic velocity and density

DEFF Research Database (Denmark)

Schutt, Derek; Lesher, Charles

2010-01-01

garnet and clinopyroxene enrichment. Using the parameterization of Schutt and Lesher (2006) we show that at cratonic mantle temperatures and pressures, orthopyroxene enrichment results in little change in bulk density (ρbulk) and shear-wave velocity (VS), but decreases compressional wave velocities (VP......We examine the modes and compositions of garnet-bearing peridotite xenoliths from the Kaapvaal Craton to quantify factors governing density and seismic velocity variations within metasomatically altered cratonic mantle. Three distinct compositional trends are resolved by principal component...... analysis. The first reflects differences in residue composition resulting from partial melting. The second is associated with orthopyroxene (opx) enrichment, possibly due to silica addition by subduction zone fluids in the source region of the xenoliths. The third principal component reflects garnet...

Origin of Fe-rich lherzolites and wehrlites from Tok, SE Siberia by reactive melt percolation in refractory mantle peridotites

Science.gov (United States)

Ionov, Dmitri A.; Chanefo, Ingrid; Bodinier, Jean-Louis

2005-10-01

Lherzolite-wehrlite (LW) series xenoliths from the quaternary Tok volcanic field in the southeastern Siberian craton are distinguished from the more common lherzolite-harzburgite (LH) series by (a) low Mg numbers (0.84-0.89) at high modal olivine (66-84%) and (b) widespread replacement of orthopyroxene (0-12%) and spinel by clinopyroxene (7-22%). The LW series peridotites are typically enriched in Ca, Fe, Mn and Ti, and depleted in Si, Ni and Cr relative to refractory LH series rocks (Mg number ≥0.89), which are metasomatised partial melting residues. Numerical modelling of Fe-Mg solid/liquid exchange during melt percolation demonstrates that LW series rocks can form by reaction of host refractory peridotites with evolved (Mg numbers 0.6-0.7), silica-undersaturated silicate melts at high melt/rock ratios, which replace orthopyroxene with clinopyroxene and decrease Mg numbers. This process is most likely related to underplating and fractionation of basaltic magma in the shallow mantle, which also produced olivine-clinopyroxene cumulates found among the Tok xenoliths.

Chromian spinel-rich black sands from eastern shoreline of ...

Indian Academy of Sciences (India)

Chromian spinel; detrital sand; ophiolites; Andaman Island; India. J. Earth Syst. .... (olivine: ol) inclusion; (e) peridotitic spinel with extensive fracturing; and (f) heavily altered rim of a peridotitic spinel. ..... The authors acknowledge the financial.

Flow in the western Mediterranean shallow mantle: Insights from xenoliths in Pliocene alkali basalts from SE Iberia (eastern Betics, Spain)

Science.gov (United States)

Hidas, Károly; Konc, Zoltán.; Garrido, Carlos J.; Tommasi, Andréa.; Vauchez, Alain; Padrón-Navarta, José Alberto; Marchesi, Claudio; Booth-Rea, Guillermo; Acosta-Vigil, Antonio; Szabó, Csaba; Varas-Reus, María. Isabel; Gervilla, Fernando

2016-11-01

Mantle xenoliths in Pliocene alkali basalts of the eastern Betics (SE Iberia, Spain) are spinel ± plagioclase lherzolite, with minor harzburgite and wehrlite, displaying porphyroclastic or equigranular textures. Equigranular peridotites have olivine crystal preferred orientation (CPO) patterns similar to those of porphyroclastic xenoliths but slightly more dispersed. Olivine CPO shows [100]-fiber patterns characterized by strong alignment of [100]-axes subparallel to the stretching lineation and a girdle distribution of [010]-axes normal to it. This pattern is consistent with simple shear or transtensional deformation accommodated by dislocation creep. One xenolith provides evidence for synkinematic reactive percolation of subduction-related Si-rich melts/fluids that resulted in oriented crystallization of orthopyroxene. Despite a seemingly undeformed microstructure, the CPO in orthopyroxenite veins in composite xenoliths is identical to those of pyroxenes in the host peridotite, suggesting late-kinematic crystallization. Based on these observations, we propose that the annealing producing the equigranular microstructures was triggered by melt percolation in the shallow subcontinental lithospheric mantle coeval to the late Neogene formation of veins in composite xenoliths. Calculated seismic properties are characterized by fast propagation of P waves and polarization of fast S waves parallel to olivine [100]-axis (stretching lineation). These data are compatible with present-day seismic anisotropy observations in SE Iberia if the foliations in the lithospheric mantle are steeply dipping and lineations are subhorizontal with ENE strike, implying dominantly horizontal mantle flow in the ENE-WSW direction within vertical planes, that is, subparallel to the paleo-Iberian margin. The measured anisotropy could thus reflect a lithospheric fabric due to strike-slip deformation in the late Miocene in the context of WSW tearing of the subducted south Iberian margin

The peculiar case of Marosticano xenoliths: a cratonic mantle fragment affected by carbonatite metasomatism in the Veneto Volcanic Province (Northern Italy)

Science.gov (United States)

Brombin, Valentina; Bonadiman, Costanza; Coltorti, Massimo; Florencia Fahnestock, M.; Bryce, Julia G.; Marzoli, Andrea

2017-04-01

The Tertiary Magmatic Province of Veneto, known as Veneto Volcanic Province (VVP), in the Northern Italy, represents one of the most important volcanic provinces of the Adria Plate. It is composed by five volcanic districts: Val d'Adige, Marosticano, Mts. Lessini, Berici Hills and Euganean Hills. Most of the volcanic products are relatively undifferentiated lavas, from nephelinites to tholeiites in composition. Commonly VVP nephelinites and basanites carry mantle xenoliths. This study presents a petrological characterization of the new xenolith occurrence of Marosticano and comparison with previously studied VVP xenolith populations (i.e. from the Lessinean and Val d'Adige areas), which represent off-craton lithospheric mantle fragment affected by Na-alkaline silicate metasomatism (Siena & Coltorti 1989; Beccaluva et al., 2001; Gasperini et al., 2006). Marosticano (MA) peridotites are anhydrous spinel-bearing lherzolites and harzburgites, which are geochemically well distinguishible from the other VVP mantle xenoliths. Primary minerals record the "most restitic" composition of the VVP sampled mantle, even calling the geochemical features of a sub-cratonic mantle. Olivines in both lherzolites and harzburgites show high Ni contents compared with the Fo values (Ni→ lherzolite: 2600-3620 ppm; harzburgite: 2600-3540 ppm; Fo → lh: 91-92; hz: 90-93) that follow the trend of olivine from a cratonic area (Kelemen, 1998). Orthopyroxenes have mg# values with 1:1 ratio with coexisting olivines and Al2O3 contents always 0.5 wt%) contents are also the chemical characteristics of the clinopyroxenes. On the whole both MA pyroxenes show major element contents that recall the characteristics of those from cratonic (sp-bearing) peridotites (e.g. from Greenland, South Africa and Tanzania; Downes et al., 2004). In addition, the relationship between the high Fo content of olivine and the high chromium contents (cr#=(Cr/(Cr+Al)X100); lh: 30-53; hz: 38-67) in coexisting spinel, out of

Two Contrasting Fabric Patterns of Olivine Observed in Garnet and Spinel Peridotite from a Mantle-derived Ultramafic Mass Enclosed in Felsic Granulite, the Moldanubian Zone, Czech Republic

Czech Academy of Sciences Publication Activity Database

Kamei, A.; Obata, M.; Michibayashi, K.; Hirajima, T.; Svojtka, Martin

2010-01-01

Roč. 51, 1/2 (2010), s. 101-123 ISSN 0022-3530 Institutional research plan: CEZ:AV0Z30130516 Keywords : garnet peridotite * spinel peridotite * olivine fabrics * Bohemian Massif Subject RIV: DB - Geology ; Mineralogy Impact factor: 3.842, year: 2010

High-temperature peridotites - lithospheric or asthenospheric?

International Nuclear Information System (INIS)

Hops, J.J.; Gurney, J.J.

1990-01-01

High-temperature peridotites by definition yield equilibration temperatures greater than 1100 degrees C. On the basis of temperature and pressure calculations, these high-temperature peridotites are amongst the deepest samples entrained by kimberlites on route to the surface. Conflicting models proposing either a lithospheric or asthenospheric origin for the high-temperature peridotites have been suggested. A detailed study of these xenoliths from a single locality, the Jagersfontein kimberlite in the Orange Free State, has been completed as a means of resolving this controversy. 10 refs., 2 figs

CO2-SO3-rich (carbonate-sulfate) melt/fluids in the lithosphere beneath El Hierro, Canary Islands.

Science.gov (United States)

Oglialoro, E.; Ferrando, S.; Malaspina, N.; Villa, I. M.; Frezzotti, M. L.

2015-12-01

Mantle xenoliths from the island of El Hierro, the youngest of the Canary Islands, have been studied to characterize fluxes of carbon in the lithosphere of an OIB volcanism region. Fifteen xenoliths (4-10 cm in diameter) were collected in a rift lava flow (15-41 ka) at a new xenolith locality in El Julan cliff (S-SW of the island). Peridotites consist of protogranular to porphyroblastic spinel harzburgites, lherzolites, and subordinate dunites. One spinel clinopyroxenite, and one olivine-websterite were also analyzed. Ultramafic xenoliths were classified as HEXO (harzburgite and dunite with exsolved orthopyroxene), HLCO (harzburgite and lherzolite containing orthopyroxene without visible exsolution lamellae), and HTR (transitional harzburgite with exsolved orthopyroxene porphyroclasts, and poikilitic orthopyroxene) following [1]. While HLCO and HTR peridotites contain mostly CO2 fluid inclusions, HEXO peridotites preserve an early association of melt/fluid inclusions containing dominantly carbonate/sulfate/silicate glass, evolving to carbonate/sulfate/phosphate/spinel aggregates, with exsolved CO2 (± carbonates, anhydrite and H2O). Chemical and Raman analyses identify dolomite, Mg-calcite, anhydrite, sulfohalite [Na6(SO4)2FCl] (± other anhydrous and hydrous alkali-sulfates), apatite, and Cr-spinel in the inclusions. Sulfides are noticeably absent. The microstructure and chemical composition of the metasomatic fluids indicate that the peridotites were infiltrated by a carbonate-sulfate-silicate melt/fluid enriched in CO2, H2O, and P. A mantle origin for this fluid is supported by high densities of CO2inclusions (> 1g/cm3), determined by Raman microspectroscopy and cross-checked by microthermometry. Consequently, El Julan peridotites provide the first evidence for liberating oxidized C and S fluxes from the Earth lithosphere in an OIB source region, and suggest that oxidation of sulfide to sulfate can occur during small-degree partial melting of the upper mantle

Origin of sapphirine- and garnet-bearing clinopyroxenite xenoliths entrained in the Jiande basalts, SE China

Science.gov (United States)

Xiao, Yan; Zhang, Hong-Fu; Liang, Zi; Su, Ben-Xun; Zhu, Bin; Sakyi, Patrick Asamoah

2018-04-01

We present petrological and geochemical data of sapphirine- and garnet-bearing clinopyroxenite xenoliths entrained in the Jiande Cenozoic basalts, SE China, to investigate their igneous and metamorphic history, and reconstruct of the thermal-tectonic evolution of the lithospheric mantle. These xenoliths have an unusual mineral association consisting of clinopyroxene + garnet/kelyphite + spinel (±sapphirine). Clinopyroxene has high Mg# (89-93) and displays convex-upward REE pattern. Garnet, partially to completely kelyphitized, is rich in pyrope end-member. It usually includes relics of spinel, suggesting that garnet was formed at the expense of spinel. The spinel has high MgO (20.8-22.9 wt%) and Al2O3 (64.8-67.9 wt%) contents. Sapphirine, forming a rim on spinel, has homogeneous SiO2 (14.5-14.9 wt%), Al2O3 (60.9-61.7 wt%) and MgO (19.7-20.1 wt%) contents, interpreted to be of metamorphic origin. The subsolidus reaction for the formation of sapphirine is as follows: spinel + garnet = sapphirine + clinopyroxene + orthopyroxene. Thus, the earliest mineral assemblage recorded in these xenoliths was spinel + clinopyroxene. The clinopyroxene in the Jiande clinopyroxenite xenoliths has Li abundances (1.04-1.63 ppm) similar to high-P mafic cumulate but much lower than those in crustal eclogite. In addition, the clinopyroxene and garnet do not show positive Eu anomalies. Therefore, the protolith of these three clinopyroxenite xenoliths was most likely a pyroxenite, originating as clinopyroxene + spinel cumulates from mafic melts percolating through the mantle. Many reaction textures such as formation of garnet and sapphirine were developed during decompression possibly coupled with cooling and melt percolation. During this process, the earlier composition of clinopyroxene and spinel also changed. The latest P-T conditions recorded in these xenoliths were at pressure of 8-10 kbar and temperatures of 1069-1094 °C. These observations imply that these rocks have been

The Anita Peridotite, New Zealand

DEFF Research Database (Denmark)

Czertowicz, Tom; Scott, James; Waight, Tod Earle

2016-01-01

–93, spinel Cr# of 70, orthopyroxene with low Al2O3, and extremely depleted whole-rock geochemical characteristics indicate that the peridotite body experienced >30% melt extraction, probably within the spinel facies. Mineral compositions show some similarity to those of cratonic peridotitic mantle. Rare Cr....../86Sr (0.705–0.706), eNd ( +6.3 to +11.1), 208Pb/204Pb (37.8–38.9) and eHf ( +5.6 to 36.9) indicate that the metasomatic agent, which caused crystallization of clinopyroxene and plagioclase, had an isotopic composition similar to ocean island basalt. On the basis of isotopic data and mineral chemistry...

Petrogenesis of ultramafic xenoliths from Hawaii inferred from Sr, Nd, and Pb isotopes

Science.gov (United States)

Okano, Osamu; Tatsumoto, Mitsunobu

Isotopic compositions of Nd, Sr, and Pb in xenoliths in the Honolulu volcanic series from the Salt Lake Crater (H-type) are similar to those of the host post-erosional basalts, but are distinct from the magma sources of Koolau shield tholeiites and MORB. In contrast, one spinel Iherzolite (K-type) has isotopic compositions of Nd and Sr that are close to those of Koolau tholeiite rather than to the other Hawaiian basalts. Previous studies have shown that Sr isotopic composition of the xenoliths and the host basalt and that trace element concentrations in minerals of garnet Iherzolites from Honolulu basalt were nearly in equilibrium with the host magma, indicating that Honolulu volcanics were derived from garnet Iherzolite or similar material. However, differences exist among the isotopic compositions (especially Nd) of the xenoliths indicating that they are accidental inclusions from upper layers. The similarity in isotopic compositions between xenoliths and Honolulu basalt suggests that the source areas in the mantle are chemically similar. Correlation of 238U/204Pb vs. 206Pb/204Pb of chrome diopside separated from the H-type spinel Iherzolites indicates that the xenoliths are 80±36 Ma, which corresponds to the lithosphere age of the Hawaiian site. This age is consistent with petrological studies [e.g., Sen and Leeman, 1991] which have found that the spinel Iherzolite inclusions are derived from the lithosphere wall rocks. The ɛNd = ˜+8 of the H-xenoliths is slightly lower than that for the East Pacific Rise MORB indicating that the xenoliths are derived from a trace element depleted source similar to the MORB residue. If the garnet Iherzolite xenoliths are derived from mixture of spinel Iherzolite with intrusive pyroxenite, then the source of the pyroxenite contained little plume component. The one exceptional spinel Iherzolite xenolith may be a residue of Koolau-like tholeiitic magma or may have been metasomatized by Koolau volcanism in the deep lithosphere

Deformation, static recrystallization, and reactive melt transport in shallow subcontinental mantle xenoliths (Tok Cenozoic volcanic field, SE Siberia)

Science.gov (United States)

Tommasi, Andréa; Vauchez, Alain; Ionov, Dmitri A.

2008-07-01

Partial melting and reactive melt transport may change the composition, microstructures, and physical properties of mantle rocks. Here we explore the relations between deformation and reactive melt transport through detailed microstructural analysis and crystallographic orientation measurements in spinel peridotite xenoliths that sample the shallow lithospheric mantle beneath the southeastern rim of the Siberian craton. These xenoliths have coarse-grained, annealed microstructures and show petrographic and chemical evidence for variable degrees of reaction with silicate melts and fluids, notably Fe-enrichment and crystallization of metasomatic clinopyroxene (cpx). Olivine crystal preferred orientations (CPO) range from strong to weak. [010]-fiber patterns, characterized by a point concentration of [010] normal to the foliation and by dispersion of [100] in the foliation plane with a weak maximum parallel to the lineation, predominate relative to the [100]-fiber patterns usually observed in lithospheric mantle xenoliths and peridotite massifs. Variations in olivine CPO patterns or intensity are not correlated with modal and chemical compositions. This, together with the analysis of microstructures, suggests that reactive melt percolation postdated both deformation and static recrystallization. Preferential crystallization of metasomatic cpx along (010) olivine grain boundaries points to an influence of the preexisting deformation fabrics on melt transport, with higher permeability along the foliation. Similarity between orthopyroxene (opx) and cpx CPO suggests that cpx orientations may be inherited from those of opx during melt-rock reaction. As observed in previous studies, reactive melt transport does not weaken olivine CPO and seismic anisotropy in the upper mantle, except in melt accumulation domains. In contrast, recovery and selective grain growth during static recrystallization may lead to development of [010]-fiber olivine CPO and, if foliations are

Immiscible melt droplets in garnet, as represented by ilmenite-magnetite-spinel spheroids in an eclogite-garnet peridotite association, Blanský les Granulite Massif, Czech Republic

Czech Academy of Sciences Publication Activity Database

Vrána, S.; Ackerman, Lukáš; Erban, V.; Halodová, P.

2016-01-01

Roč. 101, č. 1 (2016), s. 82-92 ISSN 0003-004X Institutional support: RVO:67985831 Keywords : eclogite * Fe-Ti-rich melt * garnet peridotite * garnetite * Ilmenite-magnetite-spinel * Invited Centennial article * Moldanubian Zone * UHP crystallization Subject RIV: DD - Geochemistry Impact factor: 2.021, year: 2016

The geological record of base metal sulfides in the cratonic mantle: A microscale 187Os/188Os study of peridotite xenoliths from Somerset Island, Rae Craton (Canada)

Science.gov (United States)

Bragagni, A.; Luguet, A.; Fonseca, R. O. C.; Pearson, D. G.; Lorand, J.-P.; Nowell, G. M.; Kjarsgaard, B. A.

2017-11-01

We report detailed petrographic investigations along with 187Os/188Os data in Base Metal Sulfide (BMS) on four cratonic mantle xenoliths from Somerset Island (Rae Craton, Canada). The results shed light on the processes affecting the Re-Os systematics and provide time constraints on the formation and evolution of the cratonic lithospheric mantle beneath the Rae craton. When devoid of alteration, BMS grains mainly consist of pentlandite + pyrrhotite ± chalcopyrite. The relatively high BMS modal abundance of the four investigated xenoliths cannot be reconciled with the residual nature of these peridotites, but requires addition of metasomatic BMS. This is especially evident in the two peridotites with the highest bulk Pd/Ir and Pd/Pt. Metasomatic BMS likely formed during melt/fluid percolation in the Sub Continental Lithospheric Mantle (SCLM) as well as during infiltration of the host kimberlite magma, when djerfisherite crystallized around older Fe-Ni-sulfides. On the whole-rock scale, kimberlite metasomatism is visible in a subset of bulk xenoliths, which defines a Re-Os errorchron that dates the host magma emplacement. The 187Os/188Os measured in the twenty analysed BMS grains vary from 0.1084 to >0.17 and it shows no systematic variation depending on the sulfide mineralogical assemblage. The largest range in 187Os/188Os is observed in BMS grains from the two xenoliths with the highest Pd/Ir, Pd/Pt, and sulfide modal abundance. The whole-rock TRD ages of these two samples underestimate the melting age obtained from BMS, demonstrating that bulk Re-Os model ages from peridotites with clear evidence of metasomatism should be treated with caution. The TRD ages determined in BMS grains are clustered around 2.8-2.7, ∼2.2 and ∼1.9 Ga. The 2.8-2.7 Ga TRD ages document the main SCLM building event in the Rae craton, which is likely related to the formation of the local greenstone belts in a continental rift setting. The Paleoproterozoic TRD ages can be explained by

Orogenic, Ophiolitic, and Abyssal Peridotites

Science.gov (United States)

Bodinier, J.-L.; Godard, M.

2003-12-01

"Tectonically emplaced" mantle rocks include subcontinental, suboceanic, and subarc mantle rocks that were tectonically exhumed from the upper mantle and occur:(i) as dispersed ultramafic bodies, a few meters to kilometers in size, in suture zones and mountain belts (i.e., the "alpine," or "orogenic" peridotite massifs - De Roever (1957), Thayer (1960), Den Tex (1969));(ii) as the lower ultramafic section of large (tens of kilometers) ophiolite or island arc complexes, obducted on continental margins (e.g., the Oman Ophiolite and the Kohistan Arc Complex - Coleman (1971), Boudier and Coleman (1981), Burg et al. (1998));(iii) exhumed above the sea level in ocean basins (e.g., Zabargad Island in the Red Sea, St. Paul's islets in the Atlantic and Macquarie Island in the southwestern Pacific - Tilley (1947), Melson et al. (1967), Varne and Rubenach (1972), Bonatti et al. (1981)).The "abyssal peridotites" are samples from the oceanic mantle that were dredged on the ocean floor, or recovered from drill cores (e.g., Bonatti et al., 1974; Prinz et al., 1976; Hamlyn and Bonatti, 1980).Altogether, tectonically emplaced and abyssal mantle rocks provide insights into upper mantle compositions and processes that are complementary to the information conveyed by mantle xenoliths (See Chapter 2.05). They provide coverage to vast regions of the Earth's upper mantle that are sparsely sampled by mantle xenoliths, particularly in the ocean basins and beneath passive continental margins, back-arc basins, and oceanic island arcs.Compared with mantle xenoliths, a disadvantage of some tectonically emplaced mantle rocks for representing mantle compositions is that their original geodynamic setting is not exactly known and their significance is sometimes a subject of speculation. For instance, the provenance of orogenic lherzolite massifs (subcontinental lithosphere versus upwelling asthenosphere) is still debated (Menzies and Dupuy, 1991, and references herein), as is the original setting

Petrogenetic importance of Cr - spinel metaperidotite

International Nuclear Information System (INIS)

Snarska, B.

2010-01-01

The research is ultramafic body Komarovce the site, which represents the spinel metaperidotit. In recent works dealing with the problems of genesis and tectonic ultramafic rocks placement consideration, Cr - spinel, which is considered an important petrogenetic indicator. Based on its chemical composition can further characterize the origin of peridotite.

A Dynamic study of Mantle processes applying In-situ Methods to Compound Xenoliths: implications for small to intermediate scale heterogeneity

Science.gov (United States)

Baziotis, Ioannis; Asimow, Paul; Koroneos, Antonios; Ntaflos, Theodoros; Poli, Giampero

2013-04-01

spinel lherzolite (Irving 1980). The Dish Hill volcanic field contains lherzolite xenoliths with amphibole-rich veins previously interpreted by Wilshire et al. (1980) in terms of reaction of a H2O- and Fe-rich fluid with the lherzolite host producing notable losses of Mg and Al. The Cima volcanic field, located in the southern Basin and Range province, provides samples with contacts among such diverse lithologies as Cr-diopside spinel peridotite, websterite, gabbro, clinopyroxenite and wehrlite (Wilshire et al. 1991). The San Quintin example contains large websterite veins crosscutting lherzolite matrix. Chino Valley xenoliths show cumulate textures with alternating orthopyroxene- and clinopyroxene-rich layers. We discuss and assign the observed reaction textures and mechanisms between the different minerals (e.g. olivine, clinopyroxene, orthopyroxene), layers (e.g. clinopyroxenite and lherzolite) and the consequent compositional changes across/among the minerals and the lithologic contacts. Thus, we characterize the possible genetic origin scenarios for the observed contacts between adjacent lithologies of the composite xenoliths. Those examples, most likely to represent original subsolidus contacts that underwent partial melting together, will have the most direct relevance as benchmarks for application of future kinetic models of melt extraction from heterogeneous mantle lithologies. References Irving, A.J. (1980). Petrology and Geochemistry of Composite Ultramafic Xenoliths in Alkalic Basalts and Implications for Magmatic Processes within the Mantle. American Journal of Science, 280, 389-426. Wilshire, H.G., et al. (1980). Amphibole-Rich Veins in Lherzolite Xenoliths, Dish Hill and Deadman Lake, California. American Journal of Science, 280, 576-593. Wilshire, H.G., et al. (1991). Petrology of Lower Crustal and Upper Mantle Xenoliths from the Cima Volcanic Field, California. Journal of Petrology, 32(1), 169-200.

Mg-Fe Isotope Systems of Mantle Xenoliths: Constrains on the Evolution of Siberian Craton

Science.gov (United States)

An, Y.; Kiseeva, E. S.; Sobolev, N. V.; Zhang, Z.

2017-12-01

Mantle xenoliths bring to the surface a variety of lithologies (dunites, lherzolites, harzburgites, wehrlites, eclogites, pyroxenites, and websterites) and represent snapshots of the geochemical processes that occur deep within the Earth. Recent improvements in the precision of the MC-ICP-MS measurements have allowed us to expand the amount of data on Mg and Fe isotopes for mantle-derived samples. For instance, to constrain the isotopic composition of the Earth based on the study of spinel and garnet peridotites (An et al., 2017; Teng et al., 2010), to trace the origin and to investigate the isotopic fractionation mechanism during metamorphic process using cratonic or orogenic eclogites (Li et al., 2011; Wang et al., 2012) and to reveal the metasomatism-induced mantle heterogeneity by pyroxenites (Hu et al., 2016). Numerous multi-stage modification events and mantle layering are detected in the subcontinental lithospheric mantle under the Siberian craton (Ashchepkov et al., 2008a; Sobolev et al., 1975, etc). Combined analyses of Mg and Fe isotopic systems could provide new constraints on the formation and evolution of the ancient cratonic mantle. In order to better constrain the magnitude and mechanism of inter-mineral Mg and Fe isotopic fractionations at high temperatures, systematic studies of mantle xenoliths are needed. For example, theoretical calculations and natural samples measurements have shown that large equilibrium Mg isotope fractionations controlled by the difference in coordination number of Mg among minerals could exist (Huang et al., 2013; Li et al., 2011). Thus, the Mg isotope geothermometer could help us trace the evolution history of ancient cratons. In this study we present Mg and Fe isotopic data for whole rocks and separated minerals (clinopyroxene (cpx) and garnet (grt)) from different types of mantle xenoliths (garnet pyroxenites, eclogites, grospydites and garnet peridotites) from a number of kimberlite pipes in Siberian craton (Udachnaya

Water contents of clinopyroxenes from sub-arc mantle peridotites

Science.gov (United States)

Turner, Michael; Turner, Simon; Blatter, Dawnika; Maury, Rene; Perfit, Michael; Yogodzinski, Gene

2017-01-01

One poorly constrained reservoir of the Earth's water budget is that of clinopyroxene in metasomatised, mantle peridotites. This study presents reconnaissance Sensitive High-Resolution, Ion Microprobe–Stable Isotope (SHRIMP–SI) determinations of the H2O contents of (dominantly) clinopyroxenes in rare mantle xenoliths from four different subduction zones, i.e. Mexico, Kamchatka, Philippines, and New Britain (Tabar-Feni island chain) as well as one intra-plate setting (western Victoria). All of the sub-arc xenoliths have been metasomatised and carry strong arc trace element signatures. Average measured H2O contents of the pyroxenes range from 70 ppm to 510 ppm whereas calculated bulk H2O contents range from 88 ppm to 3 737 ppm if the variable presence of amphibole is taken into account. In contrast, the intra-plate, continental mantle xenolith from western Victoria has higher water contents (3 447 ppm) but was metasomatised by alkali and/or carbonatitic melts and does not carry a subduction-related signature. Material similar to the sub-arc peridotites can either be accreted to the base of the lithosphere or potentially be transported by convection deeper into the mantle where it will lose water due to amphibole breakdown.

Peridotitic lithosphere metasomatised by volatile-bearing melts, and its association with intraplate alkaline HIMU-like magmatism

DEFF Research Database (Denmark)

Scott, James; Brenna, Marco; Crase, Jordan

2016-01-01

The role of lithospheric mantle metasomatized by CO2-bearing melts in the genesis of HIMU-like alkaline intraplate basalts is investigated using a suite of peridotite xenoliths from New Zealand. The xenoliths have Sr–Nd–Pb–Hf isotope compositions (87Sr/86Sr =0.7029, eNd = +5 to +6, 206Pb/204Pb = ...

Transition Metal Systematics of Opx-Enriched Harzburgites From the Cascades Arc With Implications for the Origin of Cratonic Peridotites

Science.gov (United States)

Turner, S. J.

2007-12-01

A number of peridotite xenoliths collected from the Simcoe volcanic field region of the Cascades arc exhibit notable enrichment of modal orthopyroxene. The process driving this enrichment is most likely metasomatism of the mantle wedge by Si-rich fluids derived ultimately from the underlying slab. By investigating the resultant elemental systematics associated with subduction zone metasomatism of this type, we hope to shed light on the origin of other opx-rich peridotites, such as those seen in many cratonic xenolith suites. The xenoliths found in the Simcoe volcanic field provide a rare opportunity to examine the composition of sub arc mantle, as it is unusual to find mantle xenoliths in volcanic arc lavas. The samples were analyzed using laser ablation ICPMS and their bulk compositions were reconstructed from point-counted mineral modes. Two-pyroxene mineral thermometry of the samples yield temperatures of approximately 1000 degrees C, corresponding to a depth of origin at uppermost mantle pressures if typical arc geotherms are assumed. Most of the peridotites are harzburgites or olivine-orthopyroxenites (Mg#s 0.88-0.9; opx mode 0.15-0.9), with small amounts of clinopyroxene (rare earths, consistent with a metasomatic origin for these opx-rich harzburgites. Of note is the counterintuitive systematics of Zn. Whole-rock Zn decreases with opx, but Zn in olivine also decreases with opx mode while Zn in opx increases with opx mode, hence the decrease in whole- rock Zn is not simply due to mechanical segregation of harzburgite into opx- and ol-rich zones. In summary, the REE signatures suggest the subducting slab as the most likely candidate for the source of the fluids that caused the opx enrichment. The opx-enrichment itself and the unusual trends in Zn suggest a reaction between a silicic fluid and normal harzburgite. Moreover, the concomitant decrease in olivine and whole-rock Zn with opx mode suggests significant leaching of Zn from the peridotite during this

Axial‐type olivine crystallographic preferred orientations: the effect of strain geometry on mantle texture

NARCIS (Netherlands)

Chatzaras, V.; Kruckenberg, Seth C.; Cohen, Shaina M.; Medaris Jr., L. Gordon; Withers, Anthony C.; Bagley, Brian

The effect of finite strain geometry on crystallographic preferred orientation (CPO) is poorly constrained in the upper mantle. Specifically, the relationship between shape preferred orientation (SPO) and CPO in the mantle rocks remains unclear. We analyzed a suite of 40 spinel peridotite xenoliths

Experimental constraints on metasomatism of mantle wedge peridotites by hybridized adakitic melts

Science.gov (United States)

Corgne, Alexandre; Schilling, Manuel E.; Grégoire, Michel; Langlade, Jessica

2018-05-01

In this study, a series of high-pressure (1.5 GPa) and high-temperature (1000-1300 °C) experiments were performed to investigate the petrological imprints of adakitic metasomatism on mantle wedge peridotites. Reaction couples were prepared using a powdered adakite from Cerro Pampa, Argentina (Mg# 0.7) placed in contact with a cored sample of medium-grained protogranular depleted spinel lherzolite from Pali Aike (Chile). Textural and chemical analyses of the run products allow us to identify key features of modal metasomatism by hybridized adakitic melts. The main changes in phase relations are associated with the following metasomatic reactions: incongruent dissolution of olivine and associated precipitation of secondary orthopyroxene, dissolution of primary spinel and subsequent replacement by secondary high-Cr spinel. In experiments with high water contents (9-12 wt%), precipitation of pargasitic amphibole also occurred, possibly at the expense of primary clinopyroxene. Neither phlogopite nor Ti-oxides were precipitated in any of these experiments. As expected, primary pyroxenes do not show evidence of being significantly altered following the interaction with the produced siliceous melts. Within the adakitic portion of the experimental charge, it was also observed the crystallization of secondary Ti-rich, Cr- and Na-poor diopsidic clinopyroxene, andesine plagioclase and, at low temperature, Fe-enriched secondary orthopyroxene. Considering textural criteria, we interpreted the formation of these minerals as crystallization products of the adakite component and not as true products of metasomatic reactions. The experimental results are used to discuss some of the petrological evidences presented to support modal metasomatism by slab-derived melts of mantle xenoliths extracted from several suprasubduction settings located around the Pacific Ring of Fire.

Spinel and plagioclase peridotites of the Nain ophiolite (Central Iran): Evidence for the incipient stage of oceanic basin formation

Science.gov (United States)

Pirnia, Tahmineh; Saccani, Emilio; Arai, Shoji

2018-06-01

The Nain ophiolites crop out along the western border of the central East Iran Microcontinent (CEIM) and consist of an ophiolitic mélange in which pargasite-bearing spinel and plagioclase mantle lherzolites are largely represented. Whole-rock and mineral chemistry data suggest that these rocks record the complex history of the asthenospheric and lithospheric mantle evolution. The spinel lherzolites have experienced low-degree ( 5%) partial melting and contain clinopyroxenes with positive Eu anomalies (Eu/Eu* = 1.10-1.48) suggesting that the partial melting occurred under oxidized conditions (fayalite-magnetite-quartz -0.8 to +1.3). The pargasite and coexisting clinopyroxene in these rocks are depleted in light rare earth elements (LREE) (mean chondrite-normalized CeN/SmN = 0.045). The depleted chemistry of this amphibole reflects metasomatism during interaction with H2O-rich subalkaline mafic melts, most likely concurrently with or after the partial melting of the spinel lherzolites. The plagioclase lherzolites were subsequently formed by the subsolidus recrystallization of spinel lherzolites under plagioclase facies conditions as a result of mantle uprising, as evidenced by: (1) the development of plagioclase rims around the spinels; (2) plagioclase + orthopyroxene exsolution textures within some clinopyroxene grains; (3) an increase in plagioclase modal content coupled with an increase in modal olivine and a decrease in modal pyroxene and pargasite; (4) coincident decreases in Al, Mg, and Ni, and increases in Cr, Ti, and Fe in spinel, as well as decreases in Al and Ca, and increases in Cr and Ti in pyroxene and pargasite; and (5) the identical whole rock compositions of the spinel and plagioclase lherzolites, which rules out a magmatic origin for the plagioclase in these units. The Nain lherzolites have similar whole-rock and mineral geochemical compositions to subcontinental peridotites that are typically representative of Iberia-type rifted continental margins

Mantle xenoliths from Nemby, Eastern Paraguay: O-Sr-Nd isotopes and trace elements of hosted clinopyroxenes

International Nuclear Information System (INIS)

Comin-Chiaramonti, P; Antonini, P; Girardi, V.A.V; Gomes, C.B; Laurora, S; Zanetti, A

2001-01-01

The Nemby spinel peridotites (Asuncion- Sapucai-Villarrica Graben, Central Eastern Paraguay) are variable in major element compositions, ranging from relatively 'fertile' to very depleted in basaltic component. Some of the xenoliths have exceeding high K 2 O (HK suite, distinct from the low K 2 O, LK-suite) and incompatible element (IE) contents compared with the composition of lherzolites which underwent partial melting during 'basalt-extraction'. The IE contents of clinopyroxenes encompass world-wide occurrences. This suggests that processes, other than depletion, occurred. Demarchi et al. (1988) have shown that K is mostly partitioned into glassy patches (blebs) in the xenoliths and glassy drops in clinopyroxenes. The blebs have been interpreted as derived from the breakdown of volatile-bearing wet phases, such as amphibole and/or phlogopite, which melted during ascent to the surface; the glassy drops in clinopyroxenes are generally interpreted as products of incongruent partial melting induced by decompression (Comin- Chiaramonti et al., 1986). Both probably represent the remnants of hydrous phases such as micas and/or amphiboles, and/or products induced by the influx of small-volume, volatile-rich melts (Petrini et al., 1994). In summary, most of the major element chemistry of the Nemby xenoliths (except for K 2 O and to a lesser extent for Na 2 O) are consistent with residual compositions after variable degrees of partial melting and metasomatic effects shown by alkali and IE enrichments in both whole rock and in clinopyroxene. Clinopyroxenes display variable REE enrichments, more evident in those crystals characterized by spongy texture and abundance of glassy drops. A possible explanation for the progressive enrichment of samples characterized by similar HREE and different LREE abundances is different ion-exchange processes (cf. 'simple mixing metasomatism model' of Song and Frey, 1989; Sen et al., 1993) due to the passage of LREE-rich chemical front on

Lower crustal xenoliths, Chinese Peak lava flow, central Sierra Nevada.

Science.gov (United States)

Dodge, F.C.W.; Calk, L.C.; Kistler, R.W.

1986-01-01

This assemblage of pyroxenite, peridotite and mafic granulite xenoliths in the toe of a 10 m.y. trachybasalt flow remnant overlying late Cretaceous granitic rocks, indicates the presence of a mafic-ultramafic complex beneath this part of central California; orthopyroxenites, websterites and clinopyroxenites are dominant. A few of the xenoliths contain ovoid opaque patches that are apparently pseudomorphs after garnet and have pyralspite garnet compositions; using a garnet-orthopyroxene geobarometer, they indicate a lower crustal depth of approx 40 km. Abundant mafic granulites can be subdivided into those with Al2O3 = or 15% and showing considerable scatter on oxide variation diagrams. The high-alumina granulite xenoliths have relatively low 87Rb/86Sr but high 87Sr/86Sr, whereas the low-alumina and ultramafic xenoliths have a wide range of 87Rb/86Sr, but lower 87Sr/86Sr; the isotopic data indicate roughly the same age as that of overlying granitic plutons (approx 100 m.y.). However, the granitic rocks have initial 87Sr/86Sr ratios intermediate between those of the high-alumina and ultramafic xenoliths, suggesting that they result from the mixing of basaltic magma (represented by the ultramafic rocks) and crustal materials, with subsequent crystal fractionation.-R.A.H.

Xenoliths from Bunyaruguru volcanic field: Some insights into lithology of East African Rift upper mantle

Science.gov (United States)

Muravyeva, N. S.; Senin, V. G.

2018-01-01

The mineral composition of mantle xenoliths from kamafugites of the Bunyaruguru volcanic field has been determined. The major and some trace elements (Si, Ti, Al, Fe, Mn, Mg, Ca, Na, K, Cr, Ni, Ba, Sr, La, Ce, Nd, Nb) has been analyzed in olivine, clinopyroxene, phlogopite, Cr-spinel, titanomagnetite, perovskite and carbonates of xenoliths and their host lavas. Bunyaruguru is one of three (Katwe-Kikorongo, Fort Portal and Bunyaruguru) volcanic fields included in the Toro-Ankole province located on the North end of the West Branch of the East African Rift. The xenoliths from three craters within the Bunyaruguru volcanic field revealed the different character of metasomatic alteration, reflecting the heterogeneity of the mantle on the kilometer scale. The most unusual finding was composite glimmerite-wehrlite xenolith from the crater Kazimiro, which contains the fresh primary high-Mg olivine with inclusions of Cr-spinel that had not been previously identified in this area. The different composition of phenocryst and xenolith minerals indicates that the studied xenoliths are not cumulus of enclosing magma, but the composition of xenoliths characterizes the lithology of the upper mantle of the area. The carbonate melt inclusions in olivine Fo90 demonstrate the existence of primary carbonatitic magmas in Bunyaruguru upper mantle. The results of texture and chemical investigation of the xenolith minerals indicate the time sequence of metasomatic alteration of Bunyaruguru upper mantle: MARID metasomatism at the first stage followed by carbonate metasomatism. The abundances of REE in perovskites from kamafugite are 2-4 times higher than similar values for xenolith. Therefore the kamafugite magma was been generated from a more enriched mantle source than the source of the xenoliths. The evaluation of P-T conditions formation of clinopyroxene xenolith revealed the range of pressure 20-65 kbar and the temperatures range 830-1040 °C. The pressure of clinopyroxene phenocryst

Cr diffusion in MgAl2O4 synthetic spinels: preliminary results

Science.gov (United States)

Freda, C.; Celata, B.; Andreozzi, G.; Perinelli, C.; Misiti, V.

2012-04-01

Chromian spinel is an accessory phase common in crustal and mantle rocks, including peridotites, gabbros and basalts. Spinel, it has been identified as one of the most effective, sensible, and versatile petrogenetic indicator in mafic and ultramafic rock systems due to the strict interdependence between its physico-chemical properties (chemical composition, cation configuration etc.) and genetic conditions (temperature, pressure, and chemical characteristics of the system). In particular, studies on intra- and inter-crystalline Mg-Fe2+, Cr-Al exchange demonstrated the close relationship between spinel composition and both degree of partial melting and equilibrium temperature of spinel-peridotites. Moreover, studies focused on the chemical zoning of Mg-Fe2+ and/or Cr-Al components in spinel have been used, combined with a diffusion model, to provide quantitative information on peridotites and gabbros pressure-temperature paths and on deformation mechanisms. Although these potentials, most of the experimental studies have been performed on spinels hosting a limited content of divalent iron (sensu stricto, MgAl2O4), whereas the scarce studies on Cr-Al inter-diffusion coefficient have been performed at 3-7 GPa as pressure boundary condition. In order to contribute to the understanding of processes occurring in the lithospheric mantle, we have initiated an experimental research project aiming at determining the Cr-Al inter-diffusion in spinel at 2 GPa pressure and temperature ranging from 1100 to 1250 °C. The experiments were performed in a end-loaded piston cylinder by using a 19 mm assembly and graphite-Pt double capsules. As starting materials we used synthetic Mg-Al spinel (200-300 μm in size) and Cr2O3 powder. Microanalyses of experimental charge were performed on polished carbon-coated mounts by electronic microprobe. Line elemental analyses were made perpendicular to the contact surface between Cr2O3 powder and spinel, at interval of 2 μm. By processing these

Petrology and geochemistry of a peridotite body in Central- Carpathian Paleogene sediments (Sedlice, eastern Slovakia

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Koppa Matúš

2014-10-01

Full Text Available We studied representative samples from a peridotite body situated NE of Sedlice village within the Central- Carpathian Paleogene sediments in the Central Western Carpathians. The relationship of the peridotite to the surrounding Paleogene sediments is not clear. The fractures of the brecciated peridotite margin are healed with secondary magnesite and calcite. On the basis of the presented bulk-rock and electron microprobe data, the wt. % amounts of mineral phases were calculated. Most of calculated “modal” compositions of this peridotite corresponds to harzburgites composed of olivine (∼70-80 wt. %, orthopyroxene (∼17-24 wt. %, clinopyroxene ( < 5 wt. % and minor spinel ( < 1 wt. %. Harzburgites could originate from lherzolitic protoliths due to a higher degree of partial melting. Rare lherzolites contain porphyroclastic 1-2 mm across orthopyroxene (up to 25 wt. %, clinopyroxene (∼ 5-8 wt. % and minor spinel ( < 0.75 wt. %. On the other hand, rare, olivine-rich dunites with scarce orthopyroxene porphyroclasts are associated with harzburgites. Metamorphic mineral assemblage of low-Al clinopyroxene (3, tremolite, chrysotile, andradite, Cr-spinel to chromite and magnetite, and an increase of fayalite component in part of olivine, indicate low-temperature metamorphic overprint. The Primitive Mantle normalized whole-rock REE patterns suggest a depleted mantle rock-suite. An increase in LREE and a positive Eu anomaly may be consequence of interactive metamorphic fluids during serpentinization. Similar rocks have been reported from the Meliatic Bôrka Nappe overlying the Central Western Carpathians orogenic wedge since the Late Cretaceous, and they could be a potential source of these peridotite blocks in the Paleogene sediments.

Recycling of Oceanic Lithosphere: Water, fO2 and Fe-isotope Constraints

Science.gov (United States)

Bizmis, M.; Peslier, A. H.; McCammon, C. A.; Keshav, S.; Williams, H. M.

2014-01-01

Spinel peridotite and garnet pyroxenite xenoliths from Hawaii provide important clues about the composition of the oceanic lithosphere, and can be used to assess its contribution to mantle heterogeneity upon recycling. The peridotites have lower bulk H2O (approximately 70-114 ppm) than the MORB source, qualitatively consistent with melt depletion. The garnet pyroxenites (high pressure cumulates) have higher H2O (200-460 ppm, up to 550 ppm accounting for phlogopite) and low H2O/Ce ratios (less than 100). The peridotites have relatively light Fe-isotopes (delta Fe -57 = -0.34 to 0.13) that decrease with increasing depletion, while the pyroxenites are significantly heavier (delta Fe-57 up to 0.3). The observed xenolith, as well as MORB and OIB total Fe-isotope variability is larger that can be explained by existing melting models. The high H2O and low H2O/Ce ratios of pyroxenites are similar to estimates of EM-type OIB sources, while their heavy delta Fe-57 are similar to some Society and Cook-Austral basalts. Therefore, recycling of mineralogically enriched oceanic lithosphere (i.e. pyroxenites) may contribute to OIB sources and mantle heterogeneity. The Fe(3+)/Sigma? systematics of these xenoliths also suggest that there might be lateral redox gradients within the lithosphere, between juxtaposed oxidized spinel peridotites (deltaFMQ = -0.7 to 1.6, at 15 kb) and more reduced pyroxenites (deltaFMQ = -2 to -0.4, at 20-25kb). Such mineralogically and compositionally imposed fO2 gradients may generate local redox melting due to changes in fluid speciation (e.g. reduced fluids from pyroxenite encountering more oxidized peridotite). Formation of such incipient, small degree melts could further contribute to metasomatic features seen in peridotites, mantle heterogeneity, as well as the low velocity and high electrical conductivity structures near the base of the lithosphere and upper mantle.

A Re-Os Study of Depleted Trench Peridotites from Northern Mariana

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Ghosh, T.; Snow, J. E.; Heri, A. R.; Brandon, A. D.; Ishizuka, O.

2017-12-01

Trench peridotites provide information about the influence of subduction initiation on the extent of mantle wedge melting. They preserve melting records throughout subduction history, and as a result, likely experience multiple melt extraction events leading to successive depletion of melt/fluid mobile major and trace elements. To track melting histories of trench peridotites, Re-Os and PGEs can be used as reliable tracers to constrain early melt extraction or re-fertilization events. The Izu-Bonin-Mariana arc, being the largest intra-oceanic subduction system, provides an excellent area to study the formation of supra-subduction zone mantle and crust. Residual peridotite (harzburgite and dunite) samples were collected by dredging from the landward slope of the northern Mariana Trench. The samples are serpentinized to various extents (typical of abyssal peridotites), leaving behind relict grains of spinel, enstatite and olivine embedded within a serpentine matrix along with occasional interstitial diopside. Major element analyses of primary minerals reveal a wide range of variations in Cr# of spinels from 0.31-0.85 indicating 16-20% of melt fraction with dunites apparently experiencing the highest amount of partial melting. For Re-Os and PGE geochemistry, samples with high amounts of spinel (>4 vol %) and variable Cr# were chosen. Initial results show that bulk rock 187Os/188Os ratios range from 0.1113 to 0.1272. All of the samples are sub-chondritic, but in some cases, they are more radiogenic than average abyssal peridotites. Os abundances vary from 1-9 ppb. Sub-chondritic values can be attributed to the samples having evolved from a Re-depleted mantle source indicating a previous melt-extraction event. The cpx-harzburgites, having lower Cr# ( 0.4) are more radiogenic than ultra depleted dunites (Cr# 0.8), which might indicate preferential removal of Os during an apparent higher degree of partial melting experienced by dunites. The higher 187Os/188Os ratios of

Silica-enriched mantle sources of subalkaline picrite-boninite-andesite island arc magmas

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Bénard, A.; Arculus, R. J.; Nebel, O.; Ionov, D. A.; McAlpine, S. R. B.

2017-02-01

Primary arc melts may form through fluxed or adiabatic decompression melting in the mantle wedge, or via a combination of both processes. Major limitations to our understanding of the formation of primary arc melts stem from the fact that most arc lavas are aggregated blends of individual magma batches, further modified by differentiation processes in the sub-arc mantle lithosphere and overlying crust. Primary melt generation is thus masked by these types of second-stage processes. Magma-hosted peridotites sampled as xenoliths in subduction zone magmas are possible remnants of sub-arc mantle and magma generation processes, but are rarely sampled in active arcs. Published studies have emphasised the predominantly harzburgitic lithologies with particularly high modal orthopyroxene in these xenoliths; the former characteristic reflects the refractory nature of these materials consequent to extensive melt depletion of a lherzolitic protolith whereas the latter feature requires additional explanation. Here we present major and minor element data for pristine, mantle-derived, lava-hosted spinel-bearing harzburgite and dunite xenoliths and associated primitive melts from the active Kamchatka and Bismarck arcs. We show that these peridotite suites, and other mantle xenoliths sampled in circum-Pacific arcs, are a distinctive peridotite type not found in other tectonic settings, and are melting residues from hydrous melting of silica-enriched mantle sources. We explore the ability of experimental studies allied with mantle melting parameterisations (pMELTS, Petrolog3) to reproduce the compositions of these arc peridotites, and present a protolith ('hybrid mantle wedge') composition that satisfies the available constraints. The composition of peridotite xenoliths recovered from erupted arc magmas plausibly requires their formation initially via interaction of slab-derived components with refractory mantle prior to or during the formation of primary arc melts. The liquid

Orthopyroxene-enrichment in the lherzolite-websterite xenolith suite from Paleogene alkali basalts of the Poiana Ruscă Mountains (Romania)

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Nédli, Zsuzsanna; Szabó, Csaba; Dégi, Júlia

2015-12-01

In this paper we present the petrography and geochemistry of a recently collected lherzolite-websterite xenolith series and of clinopyroxene xenocrysts, hosted in Upper Cretaceous-Paleogene basanites of Poiana Ruscă (Romania), whose xenoliths show notable orthopyroxene-enrichment. In the series a slightly deformed porphyroclastic-equigranular textured series could represent the early mantle characteristics, and in many cases notable orthopyroxene growth and poikilitic texture formation was observed. The most abundant mantle lithology, Type A xenoliths have high Al and Na-contents but low mg# of the pyroxenes and low cr# of spinel suggesting a low degree (Dacia block.

The Friningen Garnet Peridotite (central Swedish Caledonides). A good example of the characteristic PTt path of a cold mantle wedge garnet peridotite

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Gilio, Mattia; Clos, Frediano; van Roermund, Herman L. M.

2015-08-01

We present pseudosections of Cr-bearing garnet peridotite that together with new mineral-chemical data allow quantification of the early PT conditions of the original lithospheric mantle assemblage (M1) of the Friningen Garnet Peridotite (FGP) located in the central/middle belt of the Seve Nappe Complex in central Sweden. Results indicate that the early, coarse grained, olivine + orthopyroxene + clinopyroxene + "high Cr" garnet assemblage (M1a) was formed at 1100 ± 100 °C and 5.0 ± 0.5 GPa. These metamorphic conditions were followed by an inferred late Proterozoic exhumation event down to 850-900 °C and 1.5 GPa (M1b). The latter PT estimate is based on the breakdown of high-Cr M1a garnet (Cr# = 0.065) + olivine into an orthopyroxene + clinopyroxene + spinel (Cr# = 0.15-0.25) ± pargasite kelyphite (M1b) and the exsolution of garnet from Al-rich orthopyroxene and clinopyroxene. The M1b kelyphite is overprinted by an early-Caledonian UHPM mineral assemblage (M2; T = 800 °C and P = 3.0 GPa), equivalent to the earlier discovered UHP assemblage within an eclogitic dyke that cross-cuts FGP. In the garnet peridotite M2 is displayed by low-Cr garnet (Cr# = 0.030) growing together with spinel (Cr# = 0.35-0.45), both these minerals form part of the olivine + orthopyroxene + clinopyroxene + garnet + spinel + pargasite M2 assemblage. The formation of plagioclase + diopside symplectites after omphacite and breakdown of kyanite to sapphirine + albite in internal eclogite and the breakdown of M2 olivine + garnet to amphibole + orthopyroxene + spinel assemblages (M3) in garnet peridotite indicate post-UHP isothermal decompression down to 750-800 °C and 0.8-1.0 GPa (= M3). Multiphase solid-and fluid inclusion assemblages composed of Sr-bearing magnesite, dolomite or carbon decorate linear defect structures within M1a-b minerals and/or form subordinate local assemblages together with M2 minerals. The latter are interpreted as evidence for infiltration of early-Caledonian COH

Rhenium-osmium isotopes in pervasively metasomatized mantle xenoliths from the Bohemian Massif and implications for the reliability of Os model ages

Czech Academy of Sciences Publication Activity Database

Kochergina, Y. V.; Ackerman, Lukáš; Erban, V.; Matusiak-Malek, M.; Puziewicz, J.; Halodová, P.; Špaček, P.; Trubač, J.; Magna, T.

2016-01-01

Roč. 430, July 15 (2016), s. 90-107 ISSN 0009-2541 Institutional support: RVO:67985831 Keywords : Bohemian Massif * depletion age * Ohře/Eger rift * Os isotopes * peridotite xenolith * Re-Os * sub-continental lithospheric mantle Subject RIV: DB - Geology ; Mineralogy Impact factor: 3.347, year: 2016

Combined iron and magnesium isotope geochemistry of pyroxenite xenoliths from Hannuoba, North China Craton: implications for mantle metasomatism

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Zhao, Xin Miao; Cao, Hui Hui; Mi, Xue; Evans, Noreen J.; Qi, Yu Han; Huang, Fang; Zhang, Hong Fu

2017-06-01

We present high-precision iron and magnesium isotopic data for diverse mantle pyroxenite xenoliths collected from Hannuoba, North China Craton and provide the first combined iron and magnesium isotopic study of such rocks. Compositionally, these xenoliths range from Cr-diopside pyroxenites and Al-augite pyroxenites to garnet-bearing pyroxenites and are taken as physical evidence for different episodes of melt injection. Our results show that both Cr-diopside pyroxenites and Al-augite pyroxenites of cumulate origin display narrow ranges in iron and magnesium isotopic compositions (δ57Fe = -0.01 to 0.09 with an average of 0.03 ± 0.08 (2SD, n = 6); δ26Mg = - 0.28 to -0.25 with an average of -0.26 ± 0.03 (2SD, n = 3), respectively). These values are identical to those in the normal upper mantle and show equilibrium inter-mineral iron and magnesium isotope fractionation between coexisting mantle minerals. In contrast, the garnet-bearing pyroxenites, which are products of reactions between peridotites and silicate melts from an ancient subducted oceanic slab, exhibit larger iron isotopic variations, with δ57Fe ranging from 0.12 to 0.30. The δ57Fe values of minerals in these garnet-bearing pyroxenites also vary widely (-0.25 to 0.08 in olivines, -0.04 to 0.25 in orthopyroxenes, -0.07 to 0.31 in clinopyroxenes, 0.07 to 0.48 in spinels and 0.31-0.42 in garnets). In addition, the garnet-bearing pyroxenite shows light δ26Mg (-0.43) relative to the mantle. The δ26Mg of minerals in the garnet-bearing pyroxenite range from -0.35 for olivine and orthopyroxene, to -0.34 for clinopyroxene, 0.04 for spinel and -0.68 for garnet. These measured values stand in marked contrast to calculated equilibrium iron and magnesium isotope fractionation between coexisting mantle minerals at mantle temperatures derived from theory, indicating disequilibrium isotope fractionation. Notably, one phlogopite clinopyroxenite with an apparent later metasomatic overprint has the heaviest δ57Fe

Crystal preferred orientations of minerals from mantle xenoliths in alkali basaltic rocks form the Catalan Volcanic Zone (NE Spain)

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Fernández-Roig, Mercè; Galán, Gumer; Mariani, Elisabetta

2015-04-01

Mantle xenoliths in alkali basaltic rocks from the Catalan Volcanic Zone, associated with the Neogene-Quaternary rift system in NE Spain, are formed of anhydrous spinel lherzolites and harzburgites with minor olivine websterites. Both peridotites are considered residues of variable degrees of partial melting, later affected by metasomatism, especially the harzburgites. These and the websterites display protogranular microstructures, whereas lherzolites show continuous variation between protogranular, porphyroclastic and equigranular forms. Thermometric data of new xenoliths indicate that protogranular harzburgites, lherzolites and websterites were equilibrated at higher temperatures than porphyroclastic and equigranular lherzolites. Mineral chemistry also indicates lower equilibrium pressure for porphyroclastic and equigranular lherzolites than for the protogranular ones. Crystal preferred orientations (CPOs) of olivine and pyroxenes from these new xenoliths were determined with the EBSD-SEM technique to identify the deformation stages affecting the lithospheric mantle in this zone and to assess the relationships between the deformation fabrics, processes and microstructures. Olivine CPOs in protogranular harzburgites, lherzolites and a pyroxenite display [010]-fiber patterns characterized by a strong point concentration of the [010] axis normal to the foliation and girdle distribution of [100] and [001] axes within the foliation plane. Olivine CPO symmetry in porphyroclastic and equigranular lherzolites varies continuously from [010]-fiber to orthorhombic and [100]-fiber types. The orthorhombic patterns are characterized by scattered maxima of the three axes, which are normal between them. The rare [100]-fiber patterns display strong point concentration of [100] axis, with normal girdle distribution of the other two axes, which are aligned with each other. The patterns of pyroxene CPOs are more dispersed than those of olivine, especially for clinopyroxene, but

Silicate Veining Above an Ascending Mantle Plume - Evidence from New Ethiopian Xenolith Localities

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Rooney, T. O.; Furman, T.; Ayalew, D.; Yirgu, G.

2004-12-01

Quaternary basaltic eruptions in the Debre Zeyit (Bishoftu) and Butajira regions of the Main Ethiopian Rift host Al-augite, norite and rare lherzolite xenoliths, xenocrysts and megacrysts. These explosive basaltic eruptions are located 20 km to the west of the main rift axis and are characterized by cinder cones and maars. The host basalt was generated as a small degree partial melt of fertile peridotite between 15 and 25 kb and host abundant Al-augite (Type II) xenoliths derived from pressures up to 10 kb. The central Main Ethiopian Rift lies in a transitional zone between the continental rifting of East Africa and the sea floor spreading associated with the Red Sea. Lithospheric and sub-lithospheric processes that occur during the transition from continental to oceanic magmatism may be investigated using these xenolith-bearing basalts. Neither carbonatitic nor hydrous (amphibole + phlogopite) metasomatism is evident in either the xenoliths or host basalts, suggesting that infiltration of silicate melts that produced Al-augite veining dominates the regional lower crust and lithospheric mantle. These veins are significantly hotter (200 - 300 ° C) than the lherzolite wall rock they intrude suggesting the thermal influence of the Afar plume. Recent geophysical tomography indicates that this veining is pervasive and segmented, supporting the association of these Al-augite veins with the formation of a proto-ridge axis. Al-augite xenoliths and megacrysts have been observed in other continental rift settings such as Durango (Luhr, 2001) and Lake Baikal (Litasov, 2000), indicating Al-augite silicate melt metasomatism is a fundamental process associated with continental rift development.

Petrography and mineral chemistry of wehrlites in contact zone of gabbro intrusions and mantle peridotites of the Naein ophiolite

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Farhad Ghaseminejad

2014-10-01

, banded meta-chert, and succession of schist and marble (Davoudzadeh, 1972; Jabbari, 1997; Pirnia Naeini, 2006; Torabi, 2012; Shirdashtzadeh, 2006. In this ophiolite, the leucogabbro intrusions crosscut all other rock units. Materials and Methods Mineralogical analyses were conducted by wavelength-dispersive EPMA (JEOL JXA-8800R at the Cooperative Centre of Kanazawa University (Japan. The analyses were performed under an accelerating voltage of 15 kV and a beam current of 15 nA. JEOL software using ZAF corrections was employed for data reduction. Natural and synthetic minerals of known composition are used as standards. The Fe3+ content in minerals was estimated by assuming mineral stoichiometry. Results In the contact zone of leucogabbros and mantle peridotites of the Naein ophiolite, wehrlite and olivine clinopyroxenite are formed. Rock-forming minerals of these wehrlites are olivine (chrysolite, clinopyroxene (diopside, Cr-spinel, serpentine, amphibole (tremolite and tremolitic hornblende, epidote and magnetite. Comparison of mineral chemistry of olivine, clinopyroxene and chromian spinel in wehrlites and mantle peridotites indicate that chemical composition of clinopyroxene and olivine in these rocks are different, but chemistry of Cr-spinels in harzburgite and wehrlite are nearly same. Discussion According to the resistance of Cr-spinel against the metamorphism and alteration, it can be concluded that the wehrlites in contact zone of gabbros and mantle peridotites are formed at the expense of harzburgite. Olivine and clinopyroxene of wehrlites are formed by serpentine metamorphism and interaction of serpentine and calcium of gabbro, respectively. Field study of the research area shows that the leucogabbro intrudes the harzburgite. This research shows that after the serpentinization of mantle harzburgite, the gabbro intrusions crosscut the serpentinized peridotites, and wehrlite and olivine clinopyroxenite formed in the contact zone. Acknowledgements The authors thank

Deformation and fluid-enhanced annealing in subcontinental lithospheric mantle beneath the Pannonian Basin (Styrian Basin, Eastern Austria)

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Aradi, Laszlo; Hidas, Károly; János Kovács, István; Tommasi, Andrea; Garrido, Carlos; Szabó, Csaba

2017-04-01

In the Carpathian-Pannonian region, xenolith-bearing Neogene alkali basaltic volcanism occurred in five volcanic fields [1], from which the Styrian Basin Volcanic Field (SBVF) is the westernmost one. In this study, we present new petrographic and crystal preferred orientation (CPO) data, and structural hydroxyl ("water") contents of upper mantle xenoliths from 12 volcanic outcrops across the SBVF. The studied xenoliths are mostly coarse granular hydrous spinel lherzolites. Amphiboles, replacing pyroxenes and spinels, are present in almost every sample. The peridotites are highly annealed, olivines and pyroxenes show no significant amount of intragranular deformation. Despite the annealed texture of the peridotites, olivine CPO is unambiguous and varies between [010]-fiber, orthogonal and [100]-fiber symmetry. The CPO of pyroxenes is coherent with coeval deformation with olivine. The fabric and CPO of amphiboles suggest postkinematic epitaxial overgrowth on the precursor pyroxenes. The structural hydroxyl content of the studied xenoliths exhibits rather high, equilibrium values, up to 10, 290 and 675 ppm in olivine, ortho- and clinopyroxene, respectively. The olivines contain more structural hydroxyl in the annealed xenoliths than in the more deformed ones. The xenoliths show equilibrium temperatures from 850 to 1100 °C, which corresponds to lithospheric mantle depths between 30 and 60 km. Equilibrium temperatures show correlation with the varying CPO symmetries and grain size: coarser grained xenoliths with [100]-fiber and orthorhombic symmetry appear in the high temperature (>1000 °C) xenoliths, which is characteristic for asthenospheric environments [2]. Most of the samples display transitional CPO symmetry between [010]-fiber and orthogonal, which indicate lithospheric deformation under varying stress field from transtensional to transpressional settings [3], probably related to the Miocene evolution of the Pannonian Basin, during which varying compressive and

Compositional Variation of Chrome Spinels in the Ore-bearing Zones of the Kraka Ophiolite and the Chromitite Origin

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D. E. Saveliev

2017-07-01

Full Text Available The article considers a chemical variation of accessory and ore-forming chrome spinels from the Kraka ultramafic massif at the different scales, from the deposit to the thin section. A correlation analysis of compositional and structural features of ultramafic rocks and ores was performed. The ultramafic rocks and chromitites in the studied massif show the distinct deformation structures and tectonite olivine fabric. A typical chemical gap (i.e. Cr#=Cr/(Cr+Al was observed between peridotite, on the one hand, and dunite and chromitite, on the other hand, on the scale of deposits and ore-bearing zones. The location and size of this gap depend on the type of deposit. The gap becomes wider from the disseminated tabular bodies to the typical podiform ones. It has been found that in the thin initial dunite veinlets in peridotite the chrome spinels chemistry changes gradually and there is no Cr# gap between peridotite and dunite. The dunite venlets show a strong olivine fabric, which is an evidence of their high-temperature plastic flow origin. It has been revealed that new chrome spinel grains previously formed as rods or needles and then coarsened. We explained this observation as the result of impurity segregation, coalescence and spheroidization induced by the plastic deformation of olivine. It is inferred that a solid crystal flow is the main requirement for the dunite and chromitite body formation in the Kraka ophiolite massif. In the solid stream, the mineral phase separation takes place. For example, olivine and orthopyroxene grains of parental peridotite separate from one another, and weaker (more mobile olivine grains form dunite bodies in which chromitite appears as a result of impurity segregation.

PYROXENITE VEINS WITHIN SSZ PERIDOTITES – EVIDENCE OF MELT-ROCK INTERACTION (EGIINGOL MASSIF, MAJOR AND TRACE ELEMENT COMPOSITION OF MINERALS

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A. A. Karimov

2017-01-01

Full Text Available Evidence of melt-rock reaction between suprasubduction zone (SSZ peridotites and island arc boninititc and tholeiitic melts are identified. This process is the cause of replacive dunites and pyroxenite veins forming, which are represent the ways of island-arc melts migration. The peridotite-melt interaction is confirmed by compositional features of rocks and minerals. Influence of boninitic melt in peridotites of South Sandwich island arc leads to increasing of TiO2 and Cr-number (Cr# in spinels [Pearce et al., 2000] e.g. REE patterns of clinopyroxene from Voykar are equilibrium to boninitic melts [Belousov et al., 2009]. We show that pyroxenites are formed sequential, orthopyroxenites are originated firstly, websterites – after, and the main forming process is interaction of SSZ peridotites with percolating boninite-like melts.

Alkaline and carbonatite metasomatism of lithospheric mantle beneath SW Poland- Pilchowice case

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Ćwiek, Mateusz; Matusiak-Małek, Magdalena; Puziewicz, Jacek; Ntaflos, Theodoros

2014-05-01

The Cenozoic basanites from Pilchowice (SW Poland) form volcanic plug located exactly at Intra- Sudetic Fault. These basanites belong to the Polish part of the Central European Volcanic Province and contain numerous, usually small (pfu and mg# from 0.915- 0.920 . One xenolith contains clinopyroxene with abundant spongy rims. Primary clinopyroxene is very rare and Al-enriched (mg# 0.92, 0.17 atoms of Al pfu). The spinel is Cr enriched (cr# 0.46-0.68) and is usually associated with clinopyroxene. Orthopyroxene is depleted in REE compared to primitive mantle. Orthopyroxene from majority of xenoliths are strongly LREE depleted ((La/Lu)N = 0.03-0.21). All studied peridotites contain clinopyroxene which is enriched (2 to 70 times) in REE compared to primitive mantle. Clinopyroxene patterns show relative low HREE concentration ((La/Lu)N = 4.75- 19.99), moreover patterns from three samples are convex- upward shaped with inflection point on Nd ((La/Nd)N = 0.36-0.96). Clinopyroxene- poor lithology, high cr# in spinel and LREE- depleted nature of orthopyroxene suggest that upper mantle sampled by Pilchowice basanite is a restite after partial melting. The LREE enriched composition of clinopyroxene suggest that peridotites were metasomatised. Clinopyroxene convex- upward shaped REE plots with inflection point on Nd is typical for metasomatism related with alkaline melt. On the other hand very low ratios of Ti/ Eu (24.8- 738.9) and high (La/ Yb)N (3.5- 17) ratio (Coltorti, 1999) suggest that the metasomatic agent was either a mixture of alkaline silicate melt with carbonatite or peridotite reaction with two independent agents is recorded. This study is a part of MSc thesis of the first author and was possible thanks to the project NCN 2011/03/B/ST10/06248 of Polish National Centre for Science. Coltorti, M., Bonadiman, C., Hinton, R. W., Siena, F. & Upton, B. G. J. (1999). Carbonatite metasomatism of the oceanic upper mantle: Evidence from clinopyroxenes and glasses in

Petrography and mineral chemistry of metamorphosed mantle peridotites of Nain Ophiolite (Central Iran

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Nargess Shirdashtzadeh

2017-07-01

A at the Centre for Cooperative Research of the Kanazawa University (Kanazawa, Japan. The Micro-Raman spectroscopy (a HORIBA Jobin Yvon, LabRAM HR800 system equipped with a 532 nm Nd:YAG laser of Showa Optronics co., Ltd, J100GS-16, and an optical microscope of Olympus, BX41, Kanazawa University were used in determination of serpentine minerals. Results The lherzolite is primarily composed olivine, orthopyroxene, clinopyroxene and Cr-spinel, but secondary hydrous and non-hydrous Mg-silicate minerals have been formed during the further serpentinization and metamorphism. Lherzolite is including of olivine (~70 Vol%, forsterite-rich, orthopyroxene (~15-20 Vol%, enstatite – bronzite, clinopyroxene (5-7 Vol%, diopside - augite, and vermicular brown Cr-spinel (60-70 Vol%, chrysolite, orthopyroxene (~30 Vol%, bronzite, a small amount of clinopyroxene, and subhedral dark brown Cr-spinel, talc, tremolite, magnetite, and chlorite. Dunites are composed exclusively of olivine, minor amounts of subhedral, dark brown Cr-spinel, serpentine, metamorphic tremolite, talc and chlorite. The rocks show secondary textures of mesh, poikiloblastic, nematoblastic and jack-straw textures, but original granublastic and porphyroclastic textures are well preserved. Pyroxenes show kink bands, warped cleavages, and undulatory extinction related to metamorphic condition of upper mantle. Petrographical features indicate that a metamorphism at amphibolite facies occurred after serpentinization and chloritization of the Darreh Deh peridotites. Chrysotile cut the primary phases of olivine and pyroxene, but not the metamorphic phases of olivine neoblasts, tremolite, talc and chlorite. Some chlorite crosscut the serpentine veins, and some are in the rim of Cr-spinel and clinopyroxenes. They are mostly replaced by tremolite. Metamorphic olivines have recrystallized as fine-grained neoblasts with lower CaO content (in comparison with the primary and replacive olivines, because they have been formed at the

Orthopyroxene-enrichment in the lherzolite-websterite xenolith suite from Paleogene alkali basalts of the Poiana Ruscă Mountains (Romania

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Nédli Zsuzsanna

2015-12-01

Full Text Available In this paper we present the petrography and geochemistry of a recently collected lherzolite-websterite xenolith series and of clinopyroxene xenocrysts, hosted in Upper Cretaceous–Paleogene basanites of Poiana Ruscă (Romania, whose xenoliths show notable orthopyroxene-enrichment. In the series a slightly deformed porphyroclastic-equigranular textured series could represent the early mantle characteristics, and in many cases notable orthopyroxene growth and poikilitic texture formation was observed. The most abundant mantle lithology, Type A xenoliths have high Al and Na-contents but low mg# of the pyroxenes and low cr# of spinel suggesting a low degree (< 10 % of mafic melt removal. They are also generally poor in overall REE-s (rare earth elements and have flat REY (rare earth elements+ Y patterns with slight LREE-depletion. The geochemistry of the Type A xenoliths and calculated melt composition in equilibrium with the xenolith clinopyroxenes suggests that the percolating melt causing the poikilitization can be linked to a mafic, Al-Na-rich, volatile-poor melt and show similarity with the Late Cretaceous–Paleogene (66–72 Ma subduction-related andesitic magmatism of Poiana Ruscă. Type B xenoliths, with their slightly different chemistry, suggest that, after the ancient depletion, the mantle went through a slight metasomatic event. A subsequent passage of mafic melts in the mantle, with similar compositions to the older andesitic magmatism of Poiana Ruscă, is recorded in the pyroxenites (Fe-rich xenoliths, whereas the megacrysts seem to be cogenetic with the host basanite. The Poiana Ruscă xenoliths differ from the orthopyroxene-enriched mantle xenoliths described previously from the Carpathian-Pannonian Region and from the Dacia block.

Compositional trends among Kaapvaal Craton garnet peridotite xenoliths and their effects on seismic velocity and density

DEFF Research Database (Denmark)

Schutt, Derek; Lesher, Charles

2010-01-01

and clinopyroxene enrichment possibly as a consequence of melt infiltration. More than half of the mineral mode variance among Kaapvaal Craton xenoliths can be accounted for by opx enrichment. Melt depletion effects can account for as much as 30% of the variance, while less than 20% of the variance is associated...

Water content within the oceanic upper mantle of the Southwest Indian Ridge: a FTIR analysis of orthopyroxenes of abyssal peridotites

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Li, W.; Li, H.; Tao, C.; Jin, Z.

2013-12-01

Water can be present in the oceanic upper mantle as structural OH in nominally anhydrous minerals. Such water has marked effects on manlte melting and rheology properties. However, the water content of MORB source is mainly inferred from MORB glass data that the water budget of oceanic upper mantle is poorly constrained. Here we present water analysis of peridotites from different sites on the Southwest Indian Ridge. The mineral assemblages of these peridotites are olivine, orthopyroxene, clinopyroxene and spinel. As the peridotites have been serpentinized to different degrees, only water contents in orthopyroxnene can be better determined by FTIR spectrometry. The IR absorption bands of all measured orthopyroxenes can be devided into four different groups: (1)3562-3596 cm-1, (2)3515-3520 cm-1, (3)3415-3420 cm-1, (4)3200-3210 cm-1. The positions of these absorption bands are in good agreement with perivious reports. Hydrogen profile measurements performed on larger opx grains in each suite of samples show no obvious variations between core and rims regions, indicating that diffusion of H in orthopyroxene is insignificant. Preliminary measured water contents of orthopyroxene differ by up to one order of magnitude. Opx water contents (80-220 ppm) of most samples are within the range of those found in mantle xenoliths of contentinal settings [1]. Opx water contents of one sample (VM-21V-S9-D5-2: 38-64 ppm) are similar to those from Gakkel Ridge abyssal peridotites (25-60 ppm) [2] but higher than those from Mid-Atlantic Ridge ODP-Leg 209(~15 ppm) [3]. Two other samples show high water concentrations (VM-19ΙΙΙ-S3-TVG2-4: 260-275 ppm, Wb-18-b: 190-265 ppm) which compare well with those from Mid-Atlantic Ridge ODP-Leg 153(160-270 ppm) [4]. Most opx water contents decrease with increasing depletion degree (spl Cr#) consistent with an incompatible behavior of water during partial melting. Recalculated bulk water contents (27-117 ppm) of these peridotites overlap

The Finero phlogopite-peridotite massif: an example of subduction-related metasomatism

Science.gov (United States)

Zanetti, Alberto; Mazzucchelli, Maurizio; Rivalenti, Giorgio; Vannucci, Riccardo

The Finero peridotite massif is a harzburgite that suffered a dramatic metasomatic enrichment resulting in the pervasive presence of amphibole and phlogopite and in the sporadic occurrence of apatite and carbonate (dolomite)-bearing domains. Pyroxenite (websterite) dykes also contain phlogopite and amphibole, but are rare. Peridotite bulk-rock composition retained highly depleted major element characteristics, but was enriched in K, Rb, Ba, Sr, LREE (light rare earth elements) (LaN/YbN=8-17) and depleted in Nb. It has high radiogenic Sr (87Sr/86Sr(270)=0.7055-0.7093), low radiogenic Nd (ɛNd(270)=-1 to -3) and EMII-like Pb isotopes. Two pyroxenite - peridotite sections examined in detail show the virtual absence of major and trace element gradients in the mineral phases. In both rock types, pyroxenes and olivines have the most unfertile major element composition observed in Ivrea peridotites, spinels are the richest in Cr, and amphibole is pargasite. Clinopyroxenes exhibit LREE-enriched patterns (LaN/YbN 16), negative Ti and Zr and generally positive Sr anomaly. Amphibole has similar characteristics, except a weak negative Sr anomaly, but incompatible element concentration 1.9 (Sr) to 7.9 (Ti) times higher than that of coexisting clinopyroxene. Marked geochemical gradients occur toward apatite and carbonate-bearing domains which are randomly distributed in both the sections examined. In these regions, pyroxenes and amphibole (edenite) arelower in mg## and higher in Na2O, and spinels and phlogopite are richer in Cr2O3. Both the mineral assemblage and the incompatible trace element characteristics of the mineral phases recall the typical signatures of ``carbonatite'' metasomatism (HFSE depletion, Sr, LILE and LREE enrichment). Clinopyroxene has higher REE and Sr concentrations than amphibole (amph/cpxDREE,Sr=0.7-0.9) and lower Ti and Zr concentrations. It is proposed that the petrographic and geochemical features observed at Finero are consistent with a subduction

Syndeformation Chrome Spinels Inclusions in the Plastically Deformed Olivine Aggregates (Kraka Ophiolites, the Southern Urals

Directory of Open Access Journals (Sweden)

D. E. Saveliev

2015-12-01

Full Text Available This article presents the results of structural, petrographic, mineralogical and chemical studies of dunite veinlets in spinel peridotite from the Kraka ophiolites. It is demonstrated that plastic deformation of polycrystalline olivine, which form dunite, was accompanied by precipitation of impurities (aluminum and chrome as newly formed chrome spinels. The thinnest acicular inclusions of 0.3-0.5 micron thick are aligned in olivine grains along [010] axis. Bigger elongated irregular chrome spinel grains usually occur along grain and sub-grain olivine boundaries, and, occasionally, inside the grains along [100] axis. Alteration from the fine xenomorphic grains of chrome spinels to the bigger idiomorphic crystals was observed. Analogically to dynamic ageing (dispersion hardening in metals, the structural and chemical alterations in dunites are interpreted as deformation induced segregation of impurities. It is suggested that the euhedral chrome spinel grains typical for ophiolitic dunites were formed by coalescence and spheroidization. This process may be a key factor in the formation of ophiolitic chrome ore deposits.

Supra-subduction and mid-ocean ridge peridotites from the Piranshahr area, NW Iran

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Hajialioghli, Robab; Moazzen, Mohssen

2014-11-01

The Piranshahr metaperidotites in the northwestern end of the Zagros orogen were emplaced following the closure of the Neotethys ocean. The ophiolitic rocks were emplaced onto the passive margin of the northern edge of the Arabian plate as a result of northeastward subduction and subsequent accretion of the continental fragments. The metaperidotites have compositions ranging from low-clinopyroxene lherzolite to harzburgite and dunite. They are mantle residues with distinct geochemical signatures of both mid-ocean ridge and supra subduction zone (SSZ) affinities. The abyssal peridotites are characterized by high Al2O3 and Cr2O3 contents and low Mg-number in pyroxenes. The Cr-number in the coexisting spinel is also low. The SSZ mantle peridotites are characterized by low Al2O3 contents in pyroxenes as well as low Al2O3 and high Cr-number in spinel. Mineral chemical data indicate that the MOR- and SSZ-type peridotites are the residues from ∼15-20% and ∼30-35% of mantle melting, respectively. Considering petrography, mineralogy and textural evidence, the petrological history of the Piranshahr metaperidotites can be interpreted in three stages: mantle stable stage, serpentinization and metamorphism. The temperature conditions in the mantle are estimated using the Ca-in-orthopyroxene thermometer as 1210 ± 26 °C. The rocks have experienced serpentinization. Based on the textural observations, olivine and pyroxene transformed into lizardite and/or chrysotile with pseudomorphic textures at temperatures below 300 °C during the initial stage of serpentinization. Subsequent orogenic metamorphism affected the rocks at temperatures lower than 600 °C under lower-amphibolite facies metamorphism.

Domain structure and texture in fine grained symplectite from garnet breakdown in peridotite xenoliths (Zinst, Bavaria, Bohemian Massif)

Science.gov (United States)

Habler, G.; Špaček, P.; Abart, R.

2012-04-01

Lherzolite xenoliths entrained in Oligocene basanite at the locality of Zinst (Bavaria, western Bohemian Massif) contain rare fine-grained symplectites forming about 5 millimeter sized patches comprising several microstructurally and chemically distinct concentric zones. The symplectites reflect a complex reaction history of lherzolite during decompression and interaction with melt. Here we focus on ultra-fine grained symplectite with an integrated bulk composition expressed in terms of garnet end-member component percentages as Prp(69-71)Alm(11-13)Grs(2.5-5)And(7.5-10)Uvr(4). According to the composition and the microstructural occurrence in lherzolite the ultra-fine grained symplectite is interpreted as a product of isochemical garnet breakdown, although the precursor phase is not preserved. Under cross polarized light patches with similar extinction show a domain microstructure in symplectite. BSE images reveal an intimate intergrowth of orthopyroxene, spinel and plagioclase. All phases have a shape preferred orientation within distinct domains, whereas discontinuous SPO changes occur at microstructural domain boundaries. Three types of symplectite were microstructurally discerned: The most pristine type A occurs in a 10-30 micrometers wide zone along the symplectite margin. Spinel forms several tens of nanometers wide rods or lamellae within Opx, whereas Pl and Opx represent the symplectite matrix. All phases show a strong SPO with the maximum elongation perpendicular to the symplectite boundary. At edges of this interface, the SPO of the symplectite phases changes accordingly. Discontinuities in SPO may coincide with changes in crystallographic orientation. EBSD data showed that symplectite phases have strict crystallographic orientation relations with Opx(100)//Spl(111) and Opx(010)//Spl(110). Whereas the initial lattice orientation is controlled by adjacent phases at the symplectite boundary, the crystallographic orientation within symplectite domains

Upper mantle xenoliths from the Pliocene Kozákov volcano (NE Bohemia): P–T–fO2 and geochemical constraints

Czech Academy of Sciences Publication Activity Database

Konečný, P.; Ulrych, Jaromír; Schovánek, P.; Huraiová, M.; Řanda, Zdeněk

2006-01-01

Roč. 57, č. 5 (2006), s. 379-396 ISSN 1335-0552 R&D Projects: GA AV ČR IAA3013403 Institutional research plan: CEZ:AV0Z30130516; CEZ:AV0Z10480505 Keywords : Bohemian Massif * Cenozoic volcanism * ultramafic xenoliths * spinel lherzolite * harzburgite Subject RIV: DB - Geology ; Mineralogy Impact factor: 0.364, year: 2006 http://www.geologicacarpathica.sk/src/main.php

Characterizing the nature of melt-rock reaction in peridotites from the Santa Elena Ophiolite, NW Costa Rica

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Carr, D.; Loocke, M. P.; Snow, J. E.; Gazel, E.

2017-12-01

The Santa Elena Ophiolite (SEO), located on the northwestern coast of Costa Rica, consists primarily of preserved oceanic mantle and crustal rocks thrust above an accretionary complex. The SEO is predominantly characterized by mantle peridotites (i.e., primarily spinel lherzolite with minor amounts of harzburgite and dunite) cut and intruded by minor pegmatitic gabbros, layered gabbros, plagiogranites, and doleritic and basaltic dykes. Previous studies have concluded that the complex formed in a suprasubduction zone (SSZ) setting based on the geochemical nature of the layered gabbros and plagiogranites (i.e., depleted LREE and HFSE and enriched LILE and Pb), as well, as the peridotites (i.e., low-TiO2, Zr, and V, and high MgO, Cr, and Ni)(Denyer and Gazel, 2009). Eighteen ultramafic samples collected during the winter 2010/2011 field season (SECR11) exhibit abundant evidence for melt-rock reaction (e.g., disseminated plagioclase and plagioclase-spinel, clinopyroxene-spinel, and plagioclase-clinopyroxene symplectites) and provide a unique opportunity to characterize the textural and chemical nature of melt-rock reaction in the SEO. We present the results of a petrologic investigation (i.e., petrography and electron probe microanalysis) of 28 thin sections (19 spinel lherzolites, of which 14 are plagioclase-bearing, 4 pyroxenite veins, and 5 harzburgites) derived from the SECR11 sample set. The results of this investigation have the potential to better our understanding of the nature of melt generation and migration and melt-rock interaction in the SEO mantle section and shed further light on the complex petrogenetic history of the SEO. Denyer, P., Gazel, E., 2009, Journal of South American Earth Sciences, 28:429-442.

Oxo-amphiboles in mantle xenoliths: evidence for H2O-rich melt interacting with the lithospheric mantle of Harrow Peaks (Northern Victoria Land, Antarctica)

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Gentili, S.; Bonadiman, C.; Biagioni, C.; Comodi, P.; Coltorti, M.; Zucchini, A.; Ottolini, L.

2015-12-01

Amphiboles are the most widespread hydrous metasomatic phases in spinel-bearing mantle peridotites from Harrow Peaks (HP), Northern Victoria Land (Antarctica). They occur both in veinlets and disseminated in the peridotite matrix (preferentially associated with clinopyroxene and spinel grains). Four amphibole crystals were investigated by single-crystal X-ray diffraction (SC-XRD), electron microprobe analysis (EMPA), secondary ion mass spectrometry (SIMS) and micro-Mössbauer spectroscopy; these crystal-chemical data allow to constrain upper mantle conditions during growth of these amphiboles and the role of volatile circulation during metasomatic processes in the Antarctic region. The HP amphiboles have low Mg# values (69.3-84.1), high TiO2 (2.74-5.30 wt%) and FeOtot contents (3.40 to 6.90 wt%). The Fe3+/Fetot ratios are significantly high (0.53-0.66). The W-site is mainly occupied by O2- (0.984-1.187 apfu) plus OH (H2O: 0.70-1.01 wt%) and minor F (0.04-0.24 wt%) and Cl (0.03-0.08 wt%). Consequently, HP amphiboles are actually characterized by a significant oxo component. The aH2O values were calculated at 1.5 GPa by dehydration equilibrium equations written as H2O-buffering equilibria among end-member components of amphibole and coexisting peridotite phases. Three out of four HP amphibole-bearing peridotites have values of aH2O ranging from 0.122 to 0.335; whereas one sample has aH2O remarkably higher (0.782) approaching an ideal H2O basalt solubility. The HP fO2 values, determined by the olivine-spinel-orthopyroxene oxygeobarometer (ΔQFM = -1.77 : +0.01), are remarkably different from those calculated on the basis of the amphibole dehydration equilibrium and the application of the dissociation reaction (ΔQFM = -2.60 : +6.8). The high aH2O and the extremely high fO2 values, determined by the oxy-amphibole equilibrium with respect to the redox conditions recorded by the co-existing anhydrous minerals (close to QFM buffer), revealed that: i) the amphibole

Fragments of deeper parts of the hanging wall mantle preserved as orogenic peridotites in the central belt of the Seve Nappe Complex, Sweden

NARCIS (Netherlands)

Clos, F.; Gilio, M.; van Roermund, H.L.M.

Formation conditions of olivine microstructures are investigated in the Kittelfjäll spinel peridotite (KSP), a fragment of lithospheric mantle which occurs as an isolated body within high grade metamorphic crustal rocks of the Seve Nappe Complex (SNC), southern Västerbotten, central Sweden. The KSP

Deformation and seismic anisotropy of the subcontinental lithospheric mantle in NE Spain: EBSD data on xenoliths from the Catalan Volcanic Zone

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Fernández-Roig, Mercè; Galán, Gumer; Mariani, Elisabetta

2017-02-01

Mantle xenoliths in Neogene-Quaternary basaltic rocks related to the European Cenozoic Rift System serve to assess the evolution of the subcontinental lithospheric mantle beneath the Catalan Volcanic Zone in NE Spain. Crystallographic preferred orientations, major element composition of minerals, and temperature and pressure estimates have been used to this end. The mantle consists of spinel lherzolites, harzburgites and subordinate websterites. Protogranular microstructures are found in all peridotites and websterites, but lherzolites also display finer-grained porphyroclastic and equigranular microstructures. The dominant olivine deformation fabric is [010] fiber, but subordinate orthorhombic and [100]-fiber types are also present, especially in porphyroclastic and equigranular lherzolites. The fabric strength (J index = 10.12-1.91), equilibrium temperature and pressure are higher in xenoliths with [010]-fiber fabric and decrease in those with orthorhombic and [100]-fiber type. Incoherence between olivine and pyroxene deformation fabric is mostly found in porphyroclastic and equigranular lherzolites. Seismic anisotropy, estimated from the crystal preferred orientations, also decreases (AVp = 10.2-2.60%; AVs max = 7.95-2.19%) in porphyroclastic and equigranular lherzolites. The olivine [010]-fiber fabric points to deformation by simple shear or transpression which is likely to have occured during the development of late-Hercynian strike-slip shear zones, and to subsequent annealing during late Hercynian decompression, Permian and Cretaceous rifting. Also, it cannot be excluded that the percolation of mafic magmas during these extensional events provoked the refertilization of the lithospheric mantle. However, no clear relationship has been observed between fabric strength and mineral mode and composition. Later transtensional deformation during late Alpine orogenesis, at higher stress and decreasing temperature and pressure, transformed the earlier fabric into

Slab-derived components in the subcontinental lithospheric mantle beneath Chilean Patagonia: Geochemistry and Sr-Nd-Pb isotopes of mantle xenoliths and host basalt

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Jalowitzki, Tiago; Gervasoni, Fernanda; Conceição, Rommulo V.; Orihashi, Yuji; Bertotto, Gustavo W.; Sumino, Hirochika; Schilling, Manuel E.; Nagao, Keisuke; Morata, Diego; Sylvester, Paul

2017-11-01

In subduction zones, ultramafic xenoliths hosted in alkaline basalts can yield significant information about the role of potential slab-derived components in the subcontinental lithospheric mantle (SCLM). Chemical and isotopic heterogeneities in such xenoliths are usually interpreted to reflect melt extraction followed by metasomatic re-enrichment. Here we report new whole-rock major, trace element and isotopic (Sr-Nd-Pb) data for a Proterozoic suite of 17 anhydrous spinel-lherzolites and Eocene (new K-Ar data) host alkaline basalt found near Coyhaique ( 46°S), Aysén Region, Chile. These Patagonian nodules are located in a current back-arc position, 100 km east of the present day volcanic arc and 320 km from the Chile Trench. The mantle xenoliths consist of coarse- to medium-grained spinel-lherzolites with trace element compositions characteristic of a subduction zone setting, such as pronounced negative Nb, Ta and Ti anomalies coupled with significant enrichment of LILEs (e.g., U) and chalcophile elements (W, Pb and Sn). Most of them are characterized by flat to depleted light-rare earth element (LREE) patterns (Ce/YbN = 0.6-1.1) coupled with less radiogenic Sr-Pb (87Sr/86Sr = 0.702422-0.703479; 206Pb/204Pb = 18.212-18.539) and more radiogenic Nd isotopic compositions (143Nd/144Nd = 0.512994-0.513242), similar to the depleted mantle component (DMM or PREMA). In contrast, samples with slight LREE enrichment (Ce/YbN = 1.3-1.8) show more radiogenic Sr-Pb (87Sr/86Sr = 0.703791-0.704239; 206Pb/204Pb = 18.572-18.703) and less radiogenic Nd isotopic compositions (143Nd/144Nd = 0.512859-0.512934), similar to the EM-2 reservoir. These new geochemical and isotope data suggest that the Coyhaique spinel-lherzolites are derived from a heterogeneous SCLM resulting from mixing between a depleted mantle component and up to 10% of slab-derived components. The enriched component added to the SCLM represents variable extents of melts of both subducted Chile Trench sediments and

Deformation and hydration state of the lithospheric mantle beneath the Styrian Basin (Pannonian Basin, Eastern Austria)

Science.gov (United States)

Aradi, L. E.; Hidas, K.; Kovács, I. J.; Klébesz, R.; Szabo, C.

2016-12-01

In the Carpathian-Pannonian Region, Neogene alkali basaltic volcanism occurred in six volcanic fields, from which the Styrian Basin Volcanic Field (SBVF) is the westernmost one. In this study, we present new petrographic and crystal preferred orientation (CPO) data, and structural hydroxyl ("water") contents of upper mantle xenoliths from 12 volcanic outcrops across the SBVF. The studied xenoliths are mostly coarse granular lherzolites, amphiboles are present in almost every sample and often replace pyroxenes and spinels. The peridotites are highly annealed, olivines and pyroxenes do not show significant amount of intragranular deformation. Despite the annealed texture of the peridotites, olivine CPO is unambiguous, and varies between [010]-fiber, orthogonal and [100]-fiber symmetry. The CPO of pyroxenes is coherent with coeval deformation with olivine, showing [100]OL distributed subparallel to [001]OPX. The CPO of amphiboles suggest postkinematic epitaxial overgrowth on the precursor pyroxenes. The "water" content of the studied xenoliths exhibit rather high values, up to 10, 290 and 675 ppm in olivine, ortho- and clinopyroxene, respectively. Ortho- and clinopyroxene pairs show equilibrium in all samples, however "water" loss in olivines is observed in several xenoliths. The xenoliths show equilibrium temperatures from 850 to 1100 °C, which corresponds to lithospheric mantle depths between 30 and 60 km. Equilibrium temperatures show correlation with the varying CPO symmetries and grain size: coarser grained xenoliths with [100]-fiber and orthorhombic symmetry appear in the high temperature (>1000 °C) xenoliths, which is characteristic for asthenospheric origin. Most of the samples display transitional CPO symmetry between [010]-fiber and orthogonal, which indicate extensive lithospheric deformation under varying stress field from transtensional to transpressional settings. Based on the estimated seismic properties of the studied samples, a significant part of

Power law olivine crystal size distributions in lithospheric mantle xenoliths

Science.gov (United States)

Armienti, P.; Tarquini, S.

2002-12-01

Olivine crystal size distributions (CSDs) have been measured in three suites of spinel- and garnet-bearing harzburgites and lherzolites found as xenoliths in alkaline basalts from Canary Islands, Africa; Victoria Land, Antarctica; and Pali Aike, South America. The xenoliths derive from lithospheric mantle, from depths ranging from 80 to 20 km. Their textures vary from coarse to porphyroclastic and mosaic-porphyroclastic up to cataclastic. Data have been collected by processing digital images acquired optically from standard petrographic thin sections. The acquisition method is based on a high-resolution colour scanner that allows image capturing of a whole thin section. Image processing was performed using the VISILOG 5.2 package, resolving crystals larger than about 150 μm and applying stereological corrections based on the Schwartz-Saltykov algorithm. Taking account of truncation effects due to resolution limits and thin section size, all samples show scale invariance of crystal size distributions over almost three orders of magnitude (0.2-25 mm). Power law relations show fractal dimensions varying between 2.4 and 3.8, a range of values observed for distributions of fragment sizes in a variety of other geological contexts. A fragmentation model can reproduce the fractal dimensions around 2.6, which correspond to well-equilibrated granoblastic textures. Fractal dimensions >3 are typical of porphyroclastic and cataclastic samples. Slight bends in some linear arrays suggest selective tectonic crushing of crystals with size larger than 1 mm. The scale invariance shown by lithospheric mantle xenoliths in a variety of tectonic settings forms distant geographic regions, which indicate that this is a common characteristic of the upper mantle and should be taken into account in rheological models and evaluation of metasomatic models.

Pb and O isotope systematics in granulite facies xenoliths, French Massif Central: Implications for crustal processes

International Nuclear Information System (INIS)

Downes, H.; Kempton, P.D.; Harmon, R.S.; Briot, D.; Leyreloup, A.F.

1991-01-01

Pb and O isotope data are represented for a suite of granulite facies xenoliths found within Tertiary alkaline volcanic rocks of the Massif Central, France. The suite consists of ultramafic and mafic cumulates, metagabbros which are considered to represent basic liquids, felsic meta-igneous lithologies (charnockites) and metasediments. Ranges of δ 18 O values are +6.9 to +9.8per mille for mafic xenoliths, +9.3 to +10.2per mille for felsic meta-igneous samples and +6.1 to +11.8per mille for the metasediments. By comparison, δ 18 O values for mantle peridotites from the same region range from +5.1 to +6.9per mille, whilst local Hercynian granitoids vary from +8.6 to +12.0per mille. The 206 Pb/ 204 Pb ratios of the granulite xenoliths are between 17.77 and 19.19, 207 Pb/ 204 Pb ratios vary from 15.51 to 15.69, and 208 Pb/ 204 Pb ratios range from 38.07 to 40.07. In general, metasedimentary granulites have the more radiogenic Pb isotope compositions, whereas mafic meta-igneous samples are less radiogenic. These isotopic characteristics can be explained as the result of the interaction of mafic magmas with the metasedimentary crust into which they intruded. The release of heat also provoked melting of the more fusible parts of the lower crust and led to the formation of late-orogenic Hercynian granitoids. However, an additional component which provides less radiogenic Pb is also needed in the source of the granitoids; this may be the felsic meta-igneous xenoliths or middle/upper crustal gneisses. (orig.)

Water Content in the SW USA Mantle Lithosphere: FTIR Analysis of Dish Hill and Kilbourne Hole Pyroxenites

Science.gov (United States)

Gibler, Robert; Peslier, Anne H.; Schaffer, Lillian Aurora; Brandon, Alan D.

2014-01-01

Kilbourne Hole (NM, USA) and Dish Hill (CA, USA) mantle xenoliths sample continental mantle in two different tectonic settings. Kilbourne Hole (KH) is located in the Rio Grande rift. Dish Hill (DH) is located in the southern Mojave province, an area potentially affected by subduction of the Farallon plate beneath North America. FTIR analyses were obtained on well characterized pyroxenite, dunite and wehrlite xenoliths, thought to represent crystallized melts at mantle depths. PUM normalized REE patterns of the KH bulk-rocks are slightly LREE enriched and consistent with those of liquids generated by 6% melting of a spinel peridotite source. Pyroxenite pyroxenes have no detectable water but one DH wehrlite, which bulk-rock is LREE enriched, has 4 ppm H2O in orthopyroxene and 2 Ga. The Farallon subduction appears to have enriched in water the southwestern United States lithospheric mantle further east than DH, beneath the Colorado plateau.

Heterogeneous hydrogen distribution in orthopyroxene from veined mantle peridotite (San Carlos, Arizona): Impact of melt-rock interactions

Science.gov (United States)

Denis, Carole M. M.; Demouchy, Sylvie; Alard, Olivier

2018-03-01

Experimental studies have shown that hydrogen embedded as a trace element in mantle mineral structures affects the physical properties of mantle minerals and rocks. Nevertheless, hydrogen concentrations in mantle minerals are much lower than predicted by hydrogen solubilities obtained experimentally at high pressure and temperature. Here, we report textural analyses and major and trace element concentrations (including hydrogen) in upper mantle minerals from a spinel-bearing composite xenolith (dunite and pyroxenite) transported by silica-undersaturated mafic alkaline lavas from the San Carlos volcanic field (Arizona, USA). Our results suggest that the composite xenolith results from the percolation-reaction of a basaltic liquid within dunite channels, and is equilibrated with respect to trace elements. Equilibrium temperatures range between 1011 and 1023 °C. Hydrogen concentrations (expressed in ppm H2O by weight) obtained from unpolarized and polarized Fourier transform infrared spectroscopy are low, with average values water stored in the Earth's upper mantle.

Intracratonic asthenosphere upwelling and lithosphere rejuvenation beneath the Hoggar swell (Algeria): Evidence from HIMU metasomatised lherzolite mantle xenoliths

Science.gov (United States)

Beccaluva, L.; Azzouni-Sekkal, A.; Benhallou, A.; Bianchini, G.; Ellam, R. M.; Marzola, M.; Siena, F.; Stuart, F. M.

2007-08-01

The mantle xenoliths included in Quaternary alkaline volcanics from the Manzaz-district (Central Hoggar) are proto-granular, anhydrous spinel lherzolites. Major and trace element analyses on bulk rocks and constituent mineral phases show that the primary compositions are widely overprinted by metasomatic processes. Trace element modelling of the metasomatised clinopyroxenes allows the inference that the metasomatic agents that enriched the lithospheric mantle were highly alkaline carbonate-rich melts such as nephelinites/melilitites (or as extreme silico-carbonatites). These metasomatic agents were characterized by a clear HIMU Sr-Nd-Pb isotopic signature, whereas there is no evidence of EM1 components recorded by the Hoggar Oligocene tholeiitic basalts. This can be interpreted as being due to replacement of the older cratonic lithospheric mantle, from which tholeiites generated, by asthenospheric upwelling dominated by the presence of an HIMU signature. Accordingly, this rejuvenated lithosphere (accreted asthenosphere without any EM influence), may represent an appropriate mantle section from which deep alkaline basic melts could have been generated and shallower mantle xenoliths sampled, respectively. The available data on lherzolite xenoliths and alkaline lavas (including He isotopes, Ra Pan-African basement. This can be considered a far-field foreland reaction of the Africa-Europe collisional system since the Eocene.

Petrology and deformation style of lithospheric mantle beneath the Heldburg Dike swarm (Central Germany) subset of Central European Volcanic Province

Science.gov (United States)

Kukuła, Anna; Puziewicz, Jacek; Hidas, Károly; Ntaflos, Theodoros; Matusiak-Małek, Magdalena; Milke, Ralf

2017-04-01

The Heldburg Dike swarm is a set of Cenozoic alkali basalt dikes occurring in the central part of Germany at the border between Thuringia and Bavaria. We studied xenoliths from Strauf, Feldstein, Bramberg and from the active quarry in Zeilberg. The peridotites from Strauf, Feldstein and Bramberg have the composition of spinel lherzolite (15), spinel harzburgite (9) and dunite (3). They vary in size from 1.5 cm (Strauf) up to 20 cm (Zeilberg). We distinguish groups (A, A- and B) of peridotites based on different forsterite content in olivine. Group A consists of olivine (89.6 - 91.8 Fo), orthopyroxene (Mg# 0.90-0.93, Al 0.05-0.18 a pfu), clinopyroxene (Mg# 0.87-0.95, Al 0.06-0.26 a pfu) and spinel (Cr# 0.13-0.65, Mg# 0.54-0.78). Clinopyroxene rare earth elements (REE) patterns are S-shaped (Feldstein, Bramberg) or U-shaped (Strauf); spoon-shaped patterns occur occasionally. Trace element (TE) patterns show negative Nb, Ta, Zr, Hf, Ti and positive Th, U anomalies. The most magnesian clinopyroxene (xenolith 3140, Feldstein) is strongly aluminous and LREE depletedwith weak anomalies in TE patterns. Group A- is contains olivine (88.9-89.5 Fo), orthopyroxene (Mg# 0.89-0.90, Al 0.10-0.13 a pfu) and clinopyroxene (Mg# 0.90-0.92, Al 0.10-0.17 a pfu). Clinopyroxene is increasingly enriched in REEs from Lu to La. TE patterns are similar to those of group A but with less pronounced anomalies. Group B (3 xenoliths only) consists of olivine Fo 86.7-88.9, orthopyroxene (Mg# 0.88-0.89, Al 0.07-0.19 a pfu), clinopyroxene (Mg# 0.88-0.90, Al 0.10-0.26 a pfu). Clinopyroxene is enriched in LREE, concave upward in Pr. TE patterns are similar to those in group A. One of group B harzburgites contains grains (up to 0.5 mm) of Ca-Mg carbonate located in interstices. The clinopyroxene chemical composition plots away from the melting trend in the MgO-Al2O3 diagram of Upton et al. (2011), suggesting a later addition of the clinopyroxene. The composition of orthopyroxene corresponds to ca. 15

Experimental Melting Study of Basalt-Peridotite Hybrid Source: Constrains on Chemistry of Recycled Component

Science.gov (United States)

Gao, S.; Takahashi, E.; Matsukage, K. N.; Suzuki, T.; Kimura, J. I.

2015-12-01

It is believed that magma genesis of OIB is largely influenced by recycled oceanic crust component involved in the mantle plume (e.g., Hauri et al., 1996; Takahashi & Nakajima., 2002; Sobolev et al., 2007). Mallik & Dasgupta (2012) reported that the wall-rock reaction in MORB-eclogite and peridotite layered experiments produced a spectrum of tholeiitic to alkalic melts. However, the proper eclogite source composition is still under dispute. In order to figure out the geochemistry of recycled component as well as their melting process, we conducted a series of high-P, high-T experiments. Melting experiments (1~10hrs) were performed under 2.9GPa with Boyd-England type piston-cylinder (1460~1540°C for dry experiments, 1400~1500°C for hydrous experiments) and 5GPa with Kawai-type multi-anvil (1550~1650°C for dry experiments, 1350~1550°C for hydrous experiments), at the Magma Factory, Tokyo Tech. Spinel lherzolite KLB-1 (Takahashi 1986) was employed as peridotite component. Two basalts were used as recycled component: Fe-enriched Columbia River basalt (CRB72-180, Takahashi et al., 1998) and N-type MORB (NAM-7, Yasuda et al., 1994). In dry experiments below peridotite dry solidus, melt compositions ranged from basaltic andesite to tholeiite. Opx reaction band generated between basalt and peridotite layer hindered chemical reaction. On the other hand, alkali basalt was formed in hydrous run products because H2O promoted melting process in both layers. Compared with melts formed by N-MORB-peridotite runs, those layered experiments with CRB are enriched in FeO, TiO2, K2O and light REE at given MgO. In other words, melts produced by CRB-peridotite layered experiments are close to alkali basalts in OIB and tholeiite in Hawaii, while those by layered experiments with N-MORB are poor in above elements. Thus we propose that Fe-rich Archean or Proterozoic tholeiite (BVSP 1980) would be a possible candidate for recycled component in OIB source.

Lithosphere destabilization by melt percolation during pre-oceanic rifting: Evidence from Alpine-Apennine ophiolitic peridotites

Science.gov (United States)

Piccardo, Giovanni; Ranalli, Giorgio

2017-04-01

Orogenic peridotites from Alpine-Apennine ophiolite Massifs (Lanzo, Voltri, External and Internal Ligurides, - NW Italy, and Mt. Maggiore - Corsica) derive from the mantle lithosphere of the Ligurian Tethys. Field/structural and petrologic/geochemical studies provide constraints on the evolution of the lithospheric mantle during pre-oceanic passive rifting of the late Jurassic Ligurian Tethys ocean. Continental rifting by far-field tectonic forces induced extension of the lithosphere by means of km-scale extensional shear zones that developed before infiltration of melts from the asthenosphere (Piccardo and Vissers, 2007). After significant thinning of the lithosphere, the passively upwelling asthenosphere underwent spinel-facies decompression melting along the axial zone of the extensional system. Silica-undersaturated melt fractions percolated through the lithospheric mantle via diffuse/focused porous flow and interacted with the host peridotite through pyroxenes-dissolving/olivine-precipitating melt/rock reactions. Pyroxene dissolution and olivine precipitation modified the composition of the primary silica-undersaturated melts into derivative silica-saturated melts, while the host lithospheric spinel lherzolites were transformed into pyroxene-depleted/olivine-enriched reactive spinel harzburgites and dunites. The derivative liquids interacted through olivine-dissolving/orthopyroxene+plagioclase-crystallizing reactions with the host peridotites that were impregnated and refertilized (Piccardo et al., 2015). The saturated melts stagnated and crystallized in the shallow mantle lithosphere (as testified by diffuse interstitial crystallization of euhedral orthopyroxene and anhedral plagioclase) and locally ponded, forming orthopyroxene-rich/olivine-free gabbro-norite pods (Piccardo and Guarnieri, 2011). Reactive and impregnated peridotites are characterized by high equilibration temperatures (up to 1250 °C) even at low pressure, plagioclase-peridotite facies

Geochronological Constraints on the Exhumation and Emplacement of Subcontinental Lithospheric Mantle Peridotites in the Westernmost Mediterranean

Science.gov (United States)

Garrido, Carlos J.; Hidas, Károly; Marchesi, Claudio; Varas-Reus, María Isabel; Booth-Rea, Guillermo

2017-04-01

-subduction backarc setting for the Paleocene Alpine evolution of the Alboran peridotite massifs due to slab rollback in the westernmost Mediterranean. Several geodynamic models have proposed initial south directed migration of the orogenic arc in a more easterly position (south of the Balearic Islands) during the Paleogene before the closure of the Paleo-Tethys Ocean and collision with the Algerian margin. This early emplacement for the Ronda Peridotite (approx. 25-23 Ma) in such an easterly position would provide a common origin for the peridotite bodies found in the Kabylies in Algeria, and in the Betics-Rif. We propose that after thinning and extension in a back-arc setting recorded in the Ronda spinel tectonite domain and the recrystallization front, the final Miocene exhumation of Ronda Peridotite is associated with early folding and later but probably synkinematic shearing of the SCLM in a contractive geodynamic setting. This process is recorded in the low-pressure plagioclase tectonite domain of the Ronda peridotite and the supra-subduction bonititic affinity of late intrusive pyroxenites.

Geochemistry, mineralogy, and zircon U-Pb-Hf isotopes in peraluminous A-type granite xenoliths in Pliocene-Pleistocene basalts of northern Pannonian Basin (Slovakia)

Science.gov (United States)

Huraiová, Monika; Paquette, Jean-Louis; Konečný, Patrik; Gannoun, Abdel-Mouhcine; Hurai, Vratislav

2017-08-01

Anorogenic granite xenoliths occur in alkali basalts coeval with the Pliocene-Pleistocene continental rifting of the Pannonian Basin. Observed granite varieties include peraluminous, calcic to peralkalic, magnesian to ferroan types. Quartz and feldspars are dominant rock-forming minerals, accompanied by minor early ilmenite and late magnetite-ulvöspinel. Zircon and Nb-U-REE minerals (oxycalciopyrochlore, fergusonite, columbite) are locally abundant accessory phases in calc-alkalic types. Absence of OH-bearing Fe, Mg-silicates and presence of single homogeneous feldspars (plagioclase in calcic types, anorthoclase in calc-alkalic types, ferrian Na-sanidine to anorthoclase in alkalic types) indicate water-deficient, hypersolvus crystallization conditions. Variable volumes of interstitial glass, absence of exsolutions, and lacking deuteric hydrothermal alteration and/or metamorphic/metasomatic overprint are diagnostic of rapid quenching from hypersolidus temperatures. U-Pb zircon ages determined in calcic and calc-alkalic granite xenoliths correspond to a time interval between 5.7 and 5.2 Ma. Positive ɛHf values (14.2 ± 3.9) in zircons from a 5.2-Ma-old calc-alkalic granite xenolith indicate mantle-derived magmas largely unaffected by the assimilation of crustal material. This is in accordance with abundances of diagnostic trace elements (Rb, Y, Nb, Ta), indicating A1-type, OIB-like source magmas. Increased accumulations of Nb-U-REE minerals in these granites indicate higher degree of the magmatic differentiation reflected in Rb-enrichment, contrasting with Ba-enrichment in barren xenoliths. Incipient charnockitization, i.e. orthopyroxene and ilmenite crystallization from interstitial silicate melt, was observed in many granite xenoliths. Thermodynamic modeling using pseudosections showed that the orthopyroxene growth may have been triggered by water exsolution from the melt during ascent of xenoliths in basaltic magma. Euhedral-to-skeletal orthopyroxene growth

Interaction of extended mantle plume head with ancient lithosphere: evidence from deep-seated xenoliths in basalts and lamprophyre diatremes in Western Syria

Science.gov (United States)

Sharkov, Evgenii

2016-04-01

The Middle Cretaceous lamprophyric diatremes of the Jabel Ansaria Ridge contain xenoliths of ancient lower crustal rocks mainly represented by the suite of partly altered garnet granulite and eclogite-like rocks, which were formed at the expense of ferrogabbros and ferroclinopyroxenites most likely in the course of underplating of Fe-Ti basalt. Garnet (Alm26Grs11Py63) megacrysts and coarse-granular garnet-clinopyroxene intergrowths are most likely the varieties of rocks of this series. Garnet megacrysts are represented by large (up to 10 cm in diameter) round "nodules," often molten from the surface. Garnet is usually fractured, and the kelyphite material similar to that in rocks of the eclogite-granulite series occurs in fractures. In addition, we found several intergrowths of garnet with large (up to 3-5 cm in length) crystals of high-Al augite with the low of Ti and Na contents like in rocks of the eclogite-granulite suite. Coarse-grained garnet-clinopyroxene-hornblende rocks with spinel, as well as megacrysts of Al-Ti augite with kaersutite, form the second group in prevalence. This group is close to mantle xenoliths of the "black series" in alkali Fe-Ti basalt worldwide. Kaersutite in these rocks contains gaseous cavities, which provides evidence for the origin of rocks at the expense of a strongly fluidized melt/fluid. In contrast to rocks of the eclogite-granulite series, these rocks did not undergo alteration. Garnet Alm19-26Grs12-13.5Py59-67.5 usually associates with dark opaque spinel. In contrast, the Late Cenozoic plateaubasalts of the region practically do not contain lower crustal xenoliths, whereas xenoliths of mantle spinel lherzolite (fragments of the upper cooled rim of the plume head) are widely abundant. According to data of mineralogical thermobarometry, rocks of the eclogite-granulite suite were formed at 13.5-15.4 kbar (depths of 45-54 km) and 965-1115°C. Rocks of this suite are typical representatives of the continental lower crust

Listvenite formation from peridotite: Insights from Oman Drilling Project hole BT1B and preliminary reaction path model approach.

Science.gov (United States)

de Obeso, J. C.; Kelemen, P. B.; Manning, C. E.; Michibayashi, K.; Harris, M.

2017-12-01

Oman Drilling Project hole BT1B drilled 300 meters through the basal thrust of the Samail ophiolite. The first 200 meters of this hole are dominated by listvenites (completely carbonated peridotites) and serpentinites. Below 200 meters the hole is mainly composed of metasediments and metavolcanics. This core provides a unique record of interaction between (a) mantle peridotite in the leading edge of the mantle wedge and (b) hydrous, CO2 rich fluids derived from subducting lithologies similar to those in the metamorphic sole. We used EQ3/6 to simulate a reaction path in which hydrous fluid in equilibrium with qtz + calcite + feldspar + chlorite or smectite reacts with initially fresh peridotite at 100°C (the estimated temperature of alteration, Falk & Kelemen GCA 2015) and 5 kb. Water was first equilibrated with minerals observed during core description in the metamorphic sole at 100°C and 5kb. This fluid is then reacted with olivine enstatite and diopside (Mg#90) approximating the average composition of residual mantle peridotite (harzburgite) in Oman. Secondary minerals resulting from complete reaction are then reacted again with the initial fluid in an iterative process, up to water/rock > 1000. Water/rock close to 1 results in complete serpentinization of the peridotite, with chrysotile, brucite and magnetite as the only minerals. Water/rock >10 produces carbonates, chlorite and talc. Further increasing water/rock to > 100 produces assemblages dominated by carbonates and quartz with minor muscovite, similar to listvenites of hole BT1B that contain qtz + carbonates + Fe-oxyhydroxides + relict spinel ± chromian muscovite and fuchsite. The results of this preliminary model are consistent with the complex veining history of core from BT1B, with carbonate/iron oxide veins in both listvenites and serpentinites interpreted to be the earliest record of peridotite carbonation after initial serpentinization.

Chemical petrology of polymetamorphic ultramafic rocks from Galicia, NW Spain

NARCIS (Netherlands)

Maaskant, P.

1970-01-01

The investigated polymetamorphic peridotites occur associated with metabasic rocks in several complexes of probably Precambrian age in the northern part of the Hesperian massif (Iberian peninsula). Spinel-clinopyroxene-, spinel-pargasite-, spinel-hornblende- and chlorite-amphibole-peridotites,

Evaluation of thermobarometry for spinel lherzolite fragments in alkali basalts

Science.gov (United States)

Ozawa, Kazuhito; Youbi, Nasrrddine; Boumehdi, Moulay Ahmed; McKenzie, Dan; Nagahara, Hiroko

2017-04-01

Geothermobarometry of solid fragments in kimberlite and alkali basalts, generally called "xenoliths", provides information on thermal and chemical structure of lithospheric and asthenospheric mantle, based on which various chemical, thermal, and rheological models of lithosphere have been constructed (e.g., Griffin et al., 2003; McKenzie et al., 2005; Ave Lallemant et al., 1980). Geothermobarometry for spinel-bearing peridotite fragments, which are frequently sampled from Phanerozoic provinces in various tectonic environments (Nixon and Davies, 1987), has essential difficulties, and it is usually believed that appropriated barometers do not exist for them (O'Reilly et al., 1997; Medaris et al., 1999). Ozawa et al. (2016; EGU) proposed a method of geothermobarometry for spinel lherzolite fragments. They applied the method to mantle fragments in alkali basalts from Bou Ibalhatene maars in the Middle Atlas in Morocco (Raffone et al. 2009; El Azzouzi et al., 2010; Witting et al., 2010; El Messbahi et al., 2015). Ozawa et al. (2016) obtained 0.5GPa pressure difference (1.5-2.0GPa) for 100°C variation in temperatures (950-1050°C). However, it is imperative to verify the results on the basis of completely independent data. There are three types of independent information: (1) time scale of solid fragment extraction, which may be provided by kinetics of reactions induced by heating and/or decompression during their entrapment in the host magma and transportation to the Earth's surface (Smith, 1999), (2) depth of the host basalt formation, which may be provided by the petrological and geochemical studies of the host basalts, and (3) lithosphere-asthenosphere boundary depths, which may be estimated by geophysical observations. Among which, (3) is shown to be consistent with the result in Ozawa et al. (2016). We here present that the estimated thermal structure just before the fragment extraction is fully supported by the information of (1) and (2). Spera (1984) reviewed

Peridotite carbonation at the leading edge of the mantle wedge: OmDP Site BT1

Science.gov (United States)

Kelemen, P. B.; Godard, M.; Johnson, K. T. M.; Okazaki, K.; Manning, C. E.; Urai, J. L.; Michibayashi, K.; Harris, M.; Coggon, J. A.; Teagle, D. A. H.; Phase I Science Party, T. O. D. P.

2017-12-01

Hole BT1B sampled 3 layers of carbonated peridotite (listvenite, 0-80, 100-180, 185-197 m) separated by 2 layers of carbonate-bearing serpentinite (80-100, 180-185 m), underlain by 100 m metasediment and metabasalt. Listvenites (magnesite and/or dolomite + quartz + Fe-oxyhydroxides + chromian spinel ± fuchsite rocks) replacing mantle peridotite at and near the base of the Samail ophiolite (Stanger 85, Wilde ea 02, Nasir ea 07, Falk & Kelemen 15: FK15) reveal processes of carbon transfer into the mantle wedge (Kelemen & Manning 15) and suggest methods for CO2 capture and storage (Kelemen ea 11). Near BT1, 10 to 200 m thick tabular listvenites interlayered with partly serpentinized harzburgite have contacts parallel to the basal thrust. Imprecise Rb/Sr and 40Ar/39Ar ages indicate listvenite formed during obduction (FK15). Listvenite-peridotite contacts are gradational over 1-2 m. The listvenite matrix is microcrystalline quartz + magnesite. Quartz recrystallized from opal as in listvenites worldwide (Akbulut ea 06, Boschi ea 09, Jurkovic ea 12, Aftabi & Zarrinkoub 13, Posukhova ea 13, Ulrich ea 14) consistent with 80-120°C from clumped isotopes and phase equilibria (FK15). Thus listvenite formed - and deformed ductilely - at low T. Ubiquitous carbonate-rich veins locally comprise >10% of core sections; many have antitaxial textures consistent with expansion due to crystallization pressure. Carbonate-rich veins cut serpentinite and listvenite; veins formed a mesh, followed by replacement of mesh cores. Despite variability in and around veins, average Mg/Si, Fe/Si, Al/Si, Fe/Mg, and Cr/Al in listvenite (75 whole rocks, 7712 XRF scanner points) are indistinguishable from average Samail peridotite. CaO (average 5 wt%, range 0-40) and strongly correlated Sr were added to peridotite, most likely from subducting sediment. Rare core with >10 vol% dolomite has higher Fe/Mg than peridotite, but the same Mg/Si. Thus Mg, Si, Al and Cr, plus Fe in most rocks, were largely

Compositional and isotopic heterogeneities in the Neo-Tethyan upper mantle recorded by coexisting Al-rich and Cr-rich chromitites in the Purang peridotite massif, SW Tibet (China)

Science.gov (United States)

Xiong, Fahui; Yang, Jingsui; Xu, Xiangzhen; Kapsiotis, Argyrios; Hao, Xiaolin; Liu, Zhao

2018-06-01

The Purang harzburgite massif in SW Tibet (China) hosts abundant chrome ore deposits. Ores consist of 20 to >95% modal chromian spinel (Cr-spinel) with mylonitic fabric in imbricate shaped pods. The composition of Cr-spinel in these ores ranges from Al-rich [Cr#Sp or Cr/(Cr + Al) × 100 = 47.60-57.56] to Cr-rich (Cr#Sp: 62.55-79.57). Bulk platinum-group element (PGE) contents of chromitites are also highly variable ranging from 17.5 ppb to ∼2.5 ppm. Both metallurgical and refractory chromitites show a general enrichment in the IPGE (Os, Ir and Ru) with respect to the PPGE (Rh, Pt and Pd), resulting mostly in right-sloping primitive mantle (PM)-normalized PGE profiles. The platinum-group mineral (PGM) assemblages of both chromitite types are dominated by heterogeneously distributed, euhedral Os-bearing laurite inclusions in Cr-spinel. The Purang chromitites have quite inhomogeneous 187Os/188Os ratios (0.12289-0.13194) that are within the range of those reported for mantle-hosted chromitites from other peridotite massifs. Geochemical calculations demonstrate that the parental melts of high-Cr chromitites were boninitic, whereas those of high-Al chromitites had an arc-type tholeiitic affinity. Chromite crystallization was most likely stimulated by changes in magma compositions due to melt-peridotite interaction, leading to the establishment of a heterogeneous physicochemical environment during the early crystallization of the PGM. The highly variable PGE contents, inhomogeneous Os-isotopic compositions and varying Cr#Sp ratios of these chromitites imply a polygenetic origin for them from spatially distinct melt inputs. The generally low γOs values (different sections of a heterogeneously depleted mantle source region. These melts were most likely produced in the mantle wedge above a downgoing lithospheric slab.

Constraining the deformation and exhumation history of the Ronda Massif, Southern Spain

Science.gov (United States)

Myall, Jack; Donaldson, Colin

2016-04-01

The Ronda peridotite, southern Spain is comprised of four peridotite units hosted within metasedimentary units of the Betic Cordillera, Western Alps. These four areas of differing mineral facies are termed: the Garnet Mylonite , the Foliated Spinel Peridotite, the Granular Spinel Peridotite and the Foliated Plagioclase Peridotite. Whilst two of these units show a strong NE-SW foliation, the granular unit has no foliation and the Plagioclase facies shows a NW-SE foliation. The massif is separated from the metasedimentary host through a mylonite shear zone to the NW and thrust faults to the SE. The Garnets contain rims of Kelyphite which when combined with the rims of Spinel on the Plagioclase crystals illustrate the complicated exhumation of this massif. The Kelyphite shows the breakdown of garnet back to spinel and pyroxene showing the deeper high pressure high temperature mineral is under shallowing conditions whereas in contrast to this the low pressure low temperature plagioclase crystals have spinel rims showing that they have been moved into deeper conditions. The P-T-t pathway of the massif suggests slow exhumation to allow for partial recrystallisation of not only the garnets and plagioclases but of a 100m band of peridotite between the Foliated Spinel Peridotite and the Granular Spinel Peridotite facies. The tectonic model for the Ronda Peridotite that best describes the field data and subsequent lab work of this study is Mantle Core complex and slab roll back models. These models support mantle uprising during an extensional event that whereby slab roll back of the subducting lithosphere provides uplift into a void and emplacement into the crust. Further extension and final exhumation causes rotation of a mantle wedge into its present day position.

Isotopic characterisation of the sub-continental lithospheric mantle beneath Zealandia, a rifted fragment of Gondwana

DEFF Research Database (Denmark)

Waight, Tod Earle; Scott, James M.; van der Meer, Quinten Har Adriaan

2013-01-01

The greater New Zealand region, known as Zealandia, represents an amalgamation of crustal fragments accreted to the paleo-Pacific Gondwana margin and which underwent significant thinning during the subsequent split from Australia and Antarctica in the mid-Cretaceous following opening of the Tasma...... Sea and the Southern Ocean. We present Sr, Nd and Pb isotopes and laser ablation trace element data for a comprehensive suite of clinopyroxene separates from spinel peridotite xenoliths (lherzolite to harzburgite) from the sub-continental lithospheric mantle across southern New Zealand...... composition, age or geographical separation. These isotopic compositions indicate that the sub-continental lithospheric mantle under southern New Zealand has a regionally distinct and pervasive FOZO to HIMU – like signature. The isotopic signatures are also similar to those of the alkaline magmas...... that transported the xenoliths and suggest that most of the HIMU signature observed in the volcanics could be derived from a major source component in the sub-continental lithospheric mantle. Trace element abundances in clinopyroxene are highly heterogeneous and vary from LREE-enriched, relatively flat and MORB...

Lithospheric strength in the active boundary between the Pacific Plate and Baja California microplate constrained from lower crustal and upper mantle xenoliths

Science.gov (United States)

Chatzaras, Vasileios; van der Werf, Thomas; Kriegsman, Leo M.; Kronenberg, Andreas; Tikoff, Basil; Drury, Martyn R.

2017-04-01

The lower crust is the most poorly understood of the lithospheric layers in terms of its rheology, particularly at active plate boundaries. We studied naturally deformed lower crustal xenoliths within an active plate boundary, in order to link their microstructures and rheological parameters to the well-defined active tectonic context. The Baja California shear zone (BCSZ), located at the western boundary of the Baja California microplate, comprises the active boundary accommodating the relative motion between the Pacific plate and Baja California microplate. The basalts of the Holocene San Quintin volcanic field carry lower crustal and upper mantle xenoliths, which sample the Baja California microplate lithosphere in the vicinity of the BCSZ. The lower crustal xenoliths range from undeformed gabbros to granoblastic two-pyroxene granulites. Two-pyroxene geothermometry shows that the granulites equilibrated at temperatures of 690-920 oC. Phase equilibria (P-T pseudosections using Perple_X) indicate that symplectites with intergrown pyroxenes, plagioclase, olivine and spinel formed at 3.6-5.4 kbar, following decompression from pressures exceeding 6 kbar. FTIR spectroscopy shows that the water content of plagioclase varies among the analyzed xenoliths; plagioclase is relatively dry in two xenoliths while one xenolith contains hydrated plagioclase grains. Microstructural observations and analysis of the crystallographic texture provide evidence for deformation of plagioclase by a combination of dislocation creep and grain boundary sliding. To constrain the strength of the lower crust and upper mantle near the BCSZ we estimated the differential stress using plagioclase and olivine grain size paleopiezomtery, respectively. Differential stress estimates for plagioclase range from 10 to 32 MPa and for olivine are 30 MPa. Thus the active microplate boundary records elevated crustal temperatures, heterogeneous levels of hydration, and low strength in both the lower crust and

Further Sr and Nd isotopic results from peridotites of the Ronda Ultramafic Complex

International Nuclear Information System (INIS)

Reisberg, L.; Zindler, A.

1989-01-01

Clinopyroxenes derived from peridotites of the spinel and garnet facies of the Ronda Ultramafic Complex yield Sr and Nd isotopic ratios which extend the range of compositions found in the massif to values as depleted as 0.70205 for Sr and 0.51363 for Nd. Large-amplitude, short-wavelength isotopic variations are found to be uniquitous throughout the massif. In the garnet facies, some of these variations are shown to be produced by the tectonic disaggregation of mafic layers in an isotopically depleted peridotite matrix. Ages obtained from garnet-clinopyroxene Sm-Nd isochrons (about 22 m.y.) agree with previous determinations of the time of crustal emplacement. In the plagioclase facies, where the Sr and Nd isotopic compositions have been very strongly affected by recent cryptic metasomatism, detailed study of one sample reveals that intermineral Nd isotopic equilibrium exists between clinopyroxene, orthopyroxene, and plagioclase. This indicates that the metasomatism occurred at high temperatures, and thus probably within the mantle. A rough correlation between 143 Nd/ 144 Nd and 147 Sm/ 144 N, with an apparent 'age' of 1.3 b.y. and an initial ε Nd (0) value of +6.0, is observed among clinopyroxenes derived from river sediments from throughout the massif. This age is interpreted as the time that the massif left the convecting mantle and became incorporated into the sub-continental lithosphere. (orig.)

Spinel-rich lithologies in the lunar highland crust: Linking lunar samples, crystallization experiments and remote sensing

Science.gov (United States)

Gross, J.; Treiman, A. H.

2012-12-01

The discovery of areas rich in (Mg,Fe)-Al spinel on the rims and central peaks of lunar impact basins (by the M3 mapping spectrometer on Chandrayaan-1) has revived the old puzzle of the origin of lunar spinel. (Mg,Fe)-Al spinel is rare but widespread in lunar highlands rocks, and thus might be an important component of the lunar crust [1-3]. However, the origin of this spinel is not clear. Lunar (Mg,Fe)-Al spinel could have formed (1) during 'normal' basalt petrogenesis at high pressure; (2) during low-pressure crystallization of melts rich in olivine and plagioclase components, e.g. impact-melted lunar troctolite; or (3) formed at low pressure during assimilation of anorthosite into picritic magma; thus, lunar spinel-rich areas represent old (pre-impact) intrusions of magma. In the absence of spinel-rich samples from the Moon, however, these ideas have been highly speculative. Here we describe a rock fragment from lunar meteorite ALHA 81005 that we recently reported [4] that not only contains spinel, but is the first spinel-rich lunar sample described. This fragment contains ~30% (Mg,Fe)Al spinel and is so fine grained that it reasonably could represent a larger rock body. However, the fragment is so rich in spinel that it could not have formed by melting a peridotitic mantle or a basaltic lunar crust. The clast's small grain size and its apparent disequilibrium between spinel and pyroxene suggest fairly rapid crystallization at low pressure. It could have formed as a spinel cumulate from an impact melt of troctolitic composition; or from a picritic magma that assimilated crustal anorthosite on its margins. The latter mechanism is preferred because it explains the petrographic and chemical features of our clast, and is consistent with the regional setting of the Moscoviense spinel deposit [4]. To better understand the origin and formation history(s) of spinel-rich rocks, we also performed liquidus/crystallization experiments at low-pressure as analogues for impact

Seismic anisotropy and compositionally induced velocity anomalies in the lithosphere above mantle plumes: a petrological and microstructural study of mantle xenoliths from French Polynesia

Science.gov (United States)

Tommasi, Andréa; Godard, Marguerite; Coromina, Guilhem; Dautria, Jean-Marie; Barsczus, Hans

2004-11-01

In addition to thermal erosion, plume/lithosphere interaction may induce significant changes in the lithosphere chemical composition. To constrain the extent of this process in an oceanic environment and its consequences on the lithosphere seismic properties, we investigated the relationship between petrological processes and microstructure in mantle xenoliths from different hotspots tracks in South Pacific Superswell region: the Austral-Cook, Society, and Marquesas islands in French Polynesia. Olivine forsterite contents in the studied spinel peridotites vary continuously from Fo91 to Fo83. Dunites and wehrlites display the lowest forsterite contents. Their microstructure and high Ni contents preclude a cumulate origin, suggesting that these rocks result from melt/rock reactions involving olivine precipitation and pyroxene dissolution. In addition, lherzolites and wehrlites display evidence of late crystallization of clinopyroxene, which may result from a near-solidus melt-freezing reaction. These data suggest that the lithosphere above a mantle plume undergoes a complex sequence of magmatic processes that significantly change its composition. These compositional changes, particularly iron enrichment in olivine, result in lower P- and S-waves velocities. Relative to normal lithospheric mantle, compositionally induced seismic anomalies may attain -2.2% for S-waves and -1% for P-waves. Smaller negative anomalies for P-waves are due to a higher sensitivity to modal composition. Conversely, crystal-preferred orientations (CPO) and seismic anisotropy are little affected by these processes. Lherzolites and harzburgites, independent from composition, show high-temperature porphyroclastic microstructures and strong olivine CPO. Dunites and wehrlites display annealing microstructures to which is associated a progressive dispersion of the olivine CPO. Very weak, almost random olivine CPO is nevertheless rare, suggesting that CPO destruction is restricted to domains of

Fractional ultrabasic-basic evolution of upper-mantle magmatism: Evidence from xenoliths in kimberlites, inclusions in diamonds and experiments

Science.gov (United States)

Litvin, Yuriy; Kuzyura, Anastasia

2017-04-01

Ultrabasic peridotites and pyroxenites together with basic eclogites are the upper-mantle in situ rocks among xenoliths in kimberlites. Occasionally their diamond-bearing varieties have revealed within the xenoliths. Therewith the compositions of rock-forming minerals demonstrate features characteristic for primary diamond-included minerals of peridotite and eclogite parageneses (the elevated contents of Cr-component in peridotitic garnets and Na-jadeitic component in eclogitic clinopyroxenes). High-pressure experimental study of melting equilibria on the multicomponent peridotie-pyroxenite system olivine Ol - orthopyroxene Opx - clinopyroxene Cpx - garnet Grt showed that Opx disappeared in the peritectic reaction Opx+L→Cpx (Litvin, 1991). As a result, the invariant peritectic equilibrium Ol+Opx+Cpx+Grt+L of the ultrabasic system was found to transform into the univariant cotectic assemblage Ol+Cpx+Grt+L. Further experimental investigation showed that olivine reacts with jadeitic component (Jd) with formation of garnet at higher 4.5 GPa (Gasparik, Litvin, 1997). Study of melting relations in the multicomponent system Ol - Cpx - Jd permits to discover the peritectic point Ol+Omph+Grt+L (where Omph - omphacitic clinopyroxene) at concentration 3-4 wt.% Jd-component in the system. The reactionary loss of Opx and Ol makes it possible to transform the 4-phase garnet lherzolite ultrabasic association into the bimineral eclogite assemblage. The regime of fractional Ol, Cpx and Grt crystallization must be accompanied by increasing content of jadeitic component in residual melts that causes the complete "garnetization of olivine". In the subsequent evolution, the melts would have to fractionate for basic SiO2-saturated compositions responsible for petrogenesis of eclogite varieties marked with accessory corundum Crn, kyanite Ky and coesite Coe. Both the peritectic mechanisms occur in regime of fractional crystallization. The sequence of the upper-mantle fractional

A geochemical study of lithospheric mantle beneath Northern Victoria Land (Antarctica): main evidences from volatile content in ultramafic xenoliths

Science.gov (United States)

Correale, Alessandra; Pelorosso, Beatrice; Rizzo, Andrea Luca; Coltorti, Massimo; Italiano, Francesco; Bonadiman, Costanza

2017-04-01

A geochemical study of ultramafic xenoliths from Northern Victoria Land (Green Point, GP and Handler Ridge, HR), is carried out in order to investigate the features of the lithosphere mantle beneath the Western Antarctic Ridge System (WARS). The majority of samples is spinel anhydrous lherzolite with rare presence of secondary phases (secondary cpx and glass). Geothermobarometric calculations, based on the Fe/Mg distribution among the peridotite minerals reveal that Sub Continental Lithospheric Mantle (SCLM) beneath Handler Ridge records temperatures and redox conditions higher then Greene Point (P fixed at 15 Kbar). Moreover, geochemical models evidence that, GP mantle domain represents a residuum after ˜7 to 21 % of partial melting in the spinel stability field, which was variably affected by interaction with infiltrating melts, acting in different times, from at least Jurassic to Cenozoic (Pelorosso et al., 2016). Fluid inclusions (FI) entrapped in olivine and pyroxene crystals were investigated for elemental and isotopic contents of both, noble gases (He, Ne, Ar) and CO2. He, Ar and Ne concentrations range from 1.52×10-14 to 1.07×10-12, from 4.09×10-13 to 3.47×10-11and from 2.84×10-16 to 7.57×10-14 mol/g, respectively, while the CO2amounts are between 7.08×10-10 and 8.12×10-7 mol/g. The 3He/4He varies between 5.95 and 20.18 Ra (where Ra is the 3He/4He ratio of air), being the lowest and the highest values measured in the He-poorer samples. Post-eruptive input of cosmogenic 3He and radiogenic 4He seems to influence mainly the samples associated to a lower He concentrations, increasing and decreasing respectively their primordial 3He/4He values, that for all the other samples range between 6.76 and 7.45 Ra. This range reasonably reflects the isotope signature of mantle beneath the investigated areas. The 4He/40Ar* ratio corrected for atmospheric-derived contamination ranges between 0.004 and 0.39. The lowest 4He/40Ar* values (4He/40Ar*correspondence of

Garnet peridotite found in the Greater Antilles

Science.gov (United States)

Abbott, Richard N., Jr.; Draper, Grenville; Keshav, Shantanu

Although Alpine peridotites are relatively common in collisional orogenic zones, garnet-bearing peridotites are rare and only associated with high pressure/ultra-high pressure or temperature (HP/UHP or T) terranes [Brueckner and Medaris, 2000; Medaris, 1999]. Until recently all reported occurrences of Alpine-type garnet peridotites and HP/UHP terranes were in Eurasia and Africa, with one occurrence in the Seward Peninsula, Alaska [Till, 1981;Lieberman and Till, 1987]. Now a new Alpine-type garnet peridotite locality has been discovered in the Caribbean island of Hispaniola. This discovery is the second of its kind in the Americas.

Lithospheric magma dynamics beneath the El Hierro Volcano, Canary Islands: insights from fluid inclusions

Science.gov (United States)

Oglialoro, E.; Frezzotti, M. L.; Ferrando, S.; Tiraboschi, C.; Principe, C.; Groppelli, G.; Villa, I. M.

2017-10-01

At active volcanoes, petrological studies have been proven to be a reliable approach in defining the depth conditions of magma transport and storage in both the mantle and the crust. Based on fluid inclusion and mineral geothermobarometry in mantle xenoliths, we propose a model for the magma plumbing system of the Island of El Hierro (Canary Islands). The peridotites studied here were entrained in a lava flow exposed in the El Yulan Valley. These lavas are part of the rift volcanism that occurred on El Hierro at approximately 40-30 ka. The peridotites are spinel lherzolites, harzburgites, and dunites which equilibrated in the shallow mantle at pressures between 1.5 and 2 GPa and at temperatures between 800 and 950 °C (low-temperature peridotites; LT), as well as at higher equilibration temperatures of 900 to 1100 °C (high-temperature peridotites; HT). Microthermometry and Raman analyses of fluid inclusions reveal trapping of two distinct fluid phases: early type I metasomatic CO2-N2 fluids ( X N2 = 0.01-0.18; fluid density (d) = 1.19 g/cm3), coexisting with silicate-carbonate melts in LT peridotites, and late type II pure CO2 fluids in both LT (d = 1.11-1.00 and 0.75-0.65 g/cm3) and HT ( d = 1.04-1.11 and 0.75-0.65 g/cm3) peridotites. While type I fluids represent metasomatic phases in the deep oceanic lithosphere (at depths of 60-65 km) before the onset of magmatic activity, type II CO2 fluids testify to two fluid trapping episodes during the ascent of xenoliths in their host mafic magmas. Identification of magma accumulation zones through interpretation of type II CO2 fluid inclusions and mineral geothermobarometry indicate the presence of a vertically stacked system of interconnected small magma reservoirs in the shallow lithospheric mantle between a depth of 22 and 36 km (or 0.67 to 1 GPa). This magma accumulation region fed a short-lived magma storage region located in the lower oceanic crust at a depth of 10-12 km (or 0.26-0.34 GPa). Following our model

P-T Equilibrium Conditions of Xenoliths from the Udachnaya Kimberlite Pipe: Thermal Perturbations in the Lithospheric Mantle

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Tychkov, Nikolay; Agashev, Alexey; Malygina, Elena; Pokhilenko, Nikolay

2014-05-01

Integrated study of 250 peridotite xenoliths from Udachnaya -East pipe show difference in mineral paragenesises and textural-structural peculiarities in the different level of cratonic lithosphere mantle (CLM). The compositions of minerals were determined using EPMA. Thermobarometric parameters (Brey, Kohller, 1990) were determined for all rocks occupying different fields on geothermal curve. The deepest layer (the pressure interval of 5.0-7.0 GPa) contains mostly pophyroclastic lherzolites. Anyway, some rocks of this layer have an idiomorphic texture being also enriched in incompatible components. Higher in the CLM sequence, the interval (4.2-6.3 GPa) is composed of the most depleted rocks: megacristalline ultradepleted harzburgite-dunites and depleted granular harzburgite-dunites, as well as lherzolites in a subordinate amount. They correspond strate to 35 mW/m2 and partly overlap the deeper layer in dapth. It is likely that rocks of this layer are in equilibrium and were not subject to significant secondary changes due to kimberlite magma intrusion. Thus, this interval of the CLM sequence reflects the true (relic) geotherm for the area of the Udachnaya kimberlite pipe. Moreover, it is obvious that this interval was a major supplier of diamonds into kimberlites of the Udachnaya pipe. The interval of 4.2-2.0 GPa in the CLM sequence is also composed of coarse depleted lherzolites and harzburgites. Rocks of this interval are slightly more enriched than those of the underlying interval. This is confirmed by the distinct predominance of lherzolites over harzburgite-dunites. The heat flow in this layer varies in the range of 38-45 mW/m2 and shows a general tendency to increase with decreasing depth. According to occurrence of nonequilibrium mineral assemblages and increased heat flow relative to the major heat flow of 35 mW/m2, this interval is similar to the deepest interval of secondary enriched rocks. Interval of less than 2.0 GPa composed of spinel lherzolites and

On protolith-, metamorphic overprint, microstructure and rheology of mineral assemblages in orogenic peridotites of the central Scandinavian Caledonides

Science.gov (United States)

Gilio, Mattia; Clos, Frediano; Van Roermund, Herman L. M.

2013-04-01

central parts of the orogen), which, at least in the allochtonous nappes, have been interpreted to be "isofacial" with their host country rocks (Bucher, 1991). The latter strongly contrast to the interpretation of their "primary" (="protolith"- related) mineral assemblage(s) which clearly suggest a bimodal origin: here called thick (>80 km) versus thin (< 70 km) rooted lithospheric mantle protoliths. Distinction can be made on the basis of the presence of the stable (minimal Proterozoic) garnet-olivine assemblages in the protolith (i.e. much older than the Scandian collision event (Brueckner et al., 2010). For this reason orogenic garnet peridotite was first called "relict" garnet peridotite (Brueckner and Medaris, 2000), later rephrased into mantle wedge garnet peridotite (MWgp) by Van Roermund (2009). MWgp occurs in the WGC and in the SNC of the Upper Allochthon in central Sweden (Zhang et al., 2009). Most (All?) other protolith assemblages of orogenic peridotite in the CSC belong to the thin-rooted protolith subtype. No examples are known to us in which thin rooted prototypes became overprinted (during the Caledonian orogeny) by (U)HP metamorphic minerals, except for the subduction zone garnet peridotites (SZgp) in the WGC (Van Roermund, 2009). The latter can thus savely be interpreted as being enclosed within normal "MP" (or lower pressure) nappe sequences. As such it will be clear that this duality in protolith (and/or metamorphic) mineral assemblages of orogenic peridotite can be used to identify former, but now strongly retrogressed, (U)HP metamorphic terranes in other parts of the CSC (Gee et al, 2012). For this reason a comparative study has been made concerning field, (micro-)structural, mineral-chemical and/or geochemical aspects of two major orogenic peridotites from the SNC, central Sweden; here called the Friningen Garnet Peridotite (FGP) and the Kittelfjäll Spinel Peridotite (KSP), both exposed within the central belt of the SNC in central Sweden. The

Mantle melting and melt refertilization beneath the Southwest Indian Ridge: Mineral composition of abyssal peridotites

Science.gov (United States)

Chen, Ling; Zhu, Jihao; Chu, Fengyou; Dong, Yan-hui; Liu, Jiqiang; Li, Zhenggang; Zhu, Zhimin; Tang, Limei

2017-04-01

As one of the slowest spreading ridges of the global ocean ridge system, the Southwest Indian Ridge (SWIR) is characterized by discontinued magmatism. The 53°E segment between the Gallieni fracture zone (FZ) (52°20'E) and the Gazelle FZ (53°30'E) is a typical amagmatic segment (crustal thickness 1cm) Opx, and Mg-rich mineral compositions akin to harzburgite xenoliths that sample old continental lithospheric mantle (Kelemen et al., 1998). Melt refertilization model shows that Group 2 peridotites were affected by an enriched low-degree partial melt from the garnet stability field. These results indicate that depleted mantle which experiences ancient melting event are more sensitive to melt refertilization, thus may reduce the melt flux, leading to extremely thin crust at 53°E segment. This research was granted by the National Basic Research Programme of China (973 programme) (grant No. 2013CB429705) and the Fundamental Research Funds of Second Institute of Oceanography, State Oceanic Administration (JG1603, SZ1507). References: Johnson K T M, Dick H J B, Shimizu N. Melting in the oceanic upper mantle: An ion microprobe study of diopsides in abyssal peridotites[J]. Journal of Geophysical Research, 1990, 95(B3):2661-2678. Kelemen P B, Hart S R, Bernstein S. Silica enrichment in the continental upper mantle via melt/rock reaction[J]. Earth & Planetary Science Letters, 1998, 164(1-2):387-406. Zhou H, Dick H J. Thin crust as evidence for depleted mantle supporting the Marion Rise.[J]. Nature, 2013, 494(7436):195-200.

Calcium Isotopic Composition of Bulk Silicate Earth

Science.gov (United States)

Kang, J.; Ionov, D. A.; Liu, F.; Zhang, C.; Zhang, Z.; Huang, F.

2016-12-01

Ca isotopes are used to study the accretion history of the Earth and terrestrial planets, but, Ca isotopic composition of the Bulk Silicate Earth (BSE) remains poorly constrained [1]. To better understand the Ca isotopic composition of BSE, we analyzed 22 well studied peridotite xenoliths from Tariat (Mongolia), Vitim (southern Siberia) and Udachnaya (Siberian Craton). These samples include both fertile and highly depleted garnet and spinel peridotites that show no or only minor post-melting metasomatism or alteration. Ca isotope measurements were done on a Triton-TIMS using double spike method at the Guangzhou Institute of Geochemistry, CAS. The data are reported as δ44/40Ca (relative to NIST SRM 915a). Results for geostandards are consistent with those from other laboratories. 2 standard deviations of SRM 915a analyses are 0.13‰ (n=48). δ44/40Ca of both and fertile and refractory peridotites range from 0.79 to 1.07‰ producing an average of 0.93±0.12‰ (2SD). This value defines the Ca isotopic composition of the BSE, which is consistent with the average δ44/40Ca of oceanic basalts ( 0.90‰)[2,3]. [1] Huang et al (2010) EPSL 292; [2] Valdes et al (2014) EPSL 394; [3]DePaolo (2004) RMG 55.

Rare gases in Samoan xenoliths

Science.gov (United States)

Poreda, R. J.; Farley, K. A.

1992-09-01

The rare gas isotopic compositions of residual harzburgite xenoliths from Savai'i (SAV locality) and an unnamed seamount south of the Samoan chain (PPT locality) provide important constraints on the rare gas evolution of the mantle and atmosphere. Despite heterogeneous trace element compositions, the rare gas characteristics of the xenoliths from each of the two localities are strikingly similar. SAV and PPT xenoliths have 3He/ 4He ratios of11.1 ± 0.5 R A and21.6 ± 1 R A, respectively; this range is comparable to the 3He/ 4He ratios in Samoan lavas and clearly demonstrates that they have trapped gases from a relatively undegassed reservoir. The neon results are not consistent with mixing between MORB and a plume source with an atmospheric signature. Rather, the neon isotopes reflect either a variably degassed mantle (with a relative order of degassing of Loihi Honda et al. that the 20Ne/ 22Ne ratio in the mantle more closely resembles the solar ratio than the atmospheric one. 40Ar/ 36Ar ratios in the least contaminated samples range from 4,000 to 12,000 with the highest values in the 22 RA PPT xenoliths. There is no evidence for atmospheric 40Ar/ 36Ar ratios in the mantle source of these samples, which indicates that the lower mantle may have 40Ar/ 36Ar ratios in excess of 5,000. Xenon isotopic anomalies in 129Xe and 136Xe are as high as 6%, or about half of the maximum MORB excess and are consistent with the less degassed nature of the Samoan mantle source. These results contradict previous suggestions that the high 3He/ 4He mantle has a near-atmospheric heavy rare gas isotopic composition.

Erupted frothy xenoliths may explain lack of country-rock fragments in plutons

Science.gov (United States)

Burchardt, Steffi; Troll, Valentin R.; Schmeling, Harro; Koyi, Hemin; Blythe, Lara

2016-01-01

Magmatic stoping is discussed to be a main mechanism of magma emplacement. As a consequence of stoping, abundant country-rock fragments should occur within, and at the bottom of, magma reservoirs as “xenolith graveyards”, or become assimilated. However, the common absence of sufficient amounts of both xenoliths and crustal contamination have led to intense controversy about the efficiency of stoping. Here, we present new evidence that may explain the absence of abundant country-rock fragments in plutons. We report on vesiculated crustal xenoliths in volcanic rocks that experienced devolatilisation during heating and partial melting when entrained in magma. We hypothesise that the consequential inflation and density decrease of the xenoliths allowed them to rise and become erupted instead of being preserved in the plutonic record. Our thermomechanical simulations of this process demonstrate that early-stage xenolith sinking can be followed by the rise of a heated, partially-molten xenolith towards the top of the reservoir. There, remnants may disintegrate and mix with resident magma or erupt. Shallow-crustal plutons emplaced into hydrous country rocks may therefore not necessarily contain evidence of the true amount of magmatic stoping during their emplacement. Further studies are needed to quantify the importance of frothy xenolith in removing stoped material. PMID:27804996

Evaluation of the performance of peridotite aggregates for radiation shielding concrete

International Nuclear Information System (INIS)

Wang, Jinjun; Li, Guofeng; Meng, Dechuan

2014-01-01

Highlights: • Using peridotite rich in crystal water as aggregates of radiation-shielding concrete. • Performance of peridotite concrete is simulated and compared with ordinary concrete. • Performance of concrete samples is tested. • Neutron shielding performance can be significantly enhanced by peridotite aggregates. - Abstract: Peridotite is a kind of material that is rich in crystal water. In this paper, peridotite is used as fine and coarse aggregates for radiation shielding concrete. The transmission data of different concrete thickness and different energy neutron are calculated using Monte-Carlo method. The neutron shielding performance of the peridotite concrete samples are tested using 241 Am-Be neutron source. The results show that the peridotite is an excellent neutron shielding material

The uniquely high-temperature character of Cullinan diamonds: A signature of the Bushveld mantle plume?

Science.gov (United States)

Korolev, N. M.; Kopylova, M.; Bussweiler, Y.; Pearson, D. G.; Gurney, J.; Davidson, J.

2018-04-01

The mantle beneath the Cullinan kimberlite (formerly known as "Premier") is a unique occurrence of diamondiferous cratonic mantle where diamonds were generated contemporaneously and shortly following a mantle upwelling that led to the formation of a Large Igneous Province that produced the world's largest igneous intrusion - the 2056 Ma Bushveld Igneous Complex (BIC). We studied 332 diamond inclusions from 202 Cullinan diamonds to investigate mantle thermal effects imposed by the formation of the BIC. The overwhelming majority of diamonds come from three parageneses: (1) lithospheric eclogitic (69%), (2) lithospheric peridotitic (21%), and (3) sublithospheric mafic (9%). The lithospheric eclogitic paragenesis is represented by clinopyroxene, garnet, coesite and kyanite. Main minerals of the lithospheric peridotitic paragenesis are forsterite, enstatite, Cr-pyrope, Cr-augite and spinel; the sublithospheric mafic association includes majorite, CaSiO3 phases and omphacite. Diamond formation conditions were calculated using an Al-in-olivine thermometer, a garnet-clinopyroxene thermometer, as well as majorite and Raman barometers. The Cullinan diamonds may be unique on the global stage in recording a cold geotherm of 40 mW/m2 in cratonic lithosphere that was in contact with underlying convecting mantle at temperatures of 1450-1550 °C. The studied Cullinan diamonds contain a high proportion of inclusions equilibrated at temperatures exceeding the ambient 1327 °C adiabat, i.e. 54% of eclogitic diamonds and 41% of peridotitic diamonds. By contrast, ≤ 1% of peridotitic diamond inclusions globally yield equally high temperatures. We propose that the Cullinan diamond inclusions recorded transient, slow-dissipating thermal perturbations associated with the plume-related formation of the 2 Ga Bushveld igneous province. The presence of inclusions in diamond from the mantle transition zone at 300-650 km supports this view. Cullinan xenoliths indicative of the thermal state of

Calcium isotopic composition of mantle peridotites

Science.gov (United States)

Huang, F.; Kang, J.; Zhang, Z.

2015-12-01

Ca isotopes are useful to decipher mantle evolution and the genetic relationship between the Earth and chondrites. It has been observed that Ca isotopes can be fractionated at high temperature [1-2]. However, Ca isotopic composition of the mantle peridotites and fractionation mechanism are still poorly constrained. Here, we report Ca isotope composition of 12 co-existing pyroxene pairs in 10 lherzolites, 1 harzburgite, and 1 wehrlite xenoliths collected from Hainan Island (South Eastern China). Ca isotope data were measured on a Triton-TIMS using the double spike method at the Guangzhou Institute of Geochemistry, CAS. The long-term external error is 0.12‰ (2SD) based on repeated analyses of NIST SRM 915a and geostandards. δ44Ca of clinopyroxenes except that from the wehrlite ranges from 0.85‰ to 1.14‰, while opx yields a wide range from 0.98‰ up to 2.16‰. Co-existing pyroxene pairs show large Δ44Caopx-cpx (defined as δ44Caopx-δ44Cacpx) ranging from 0 to 1.23‰, reflecting equilibrium fractionation controlled by variable Ca contents in the opx. Notably, clinopyroxene of wehrlite shows extremely high δ44Ca (3.22‰). δ44Ca of the bulk lherzolites and harzburgites range from 0.86‰ to 1.14‰. This can be explained by extracting melts with slightly light Ca isotopic compositions. Finally, the high δ44Ca of the wehrlite (3.22‰) may reflect metasomatism by melt which has preferentially lost light Ca isotopes due to chemical diffusion during upwelling through the melt channel. [1] Amini et al (2009) GGR 33; [2] Huang et al (2010) EPSL 292.

New constraints on the textural and geochemical evolution of the upper mantle beneath the Styrian basin

Science.gov (United States)

Aradi, Laszlo; Hidas, Károly; Zanetti, Alberto; János Kovács, István; Patkó, Levente; Szabó, Csaba

2016-04-01

Plio-Pleistocene alkali basaltic volcanism sampled sporadically the upper mantle beneath the Carpathian-Pannonian Region (CPR, e.g. [1]). Lavas and pyroclasts often contain mantle derived xenoliths, and the majority of them have been extensively studied [1], except the westernmost Styrian Basin Volcanic Field (SBVF, Eastern Austria and Slovenia). In the SBVF only a few volcanic centers have been studied in details (e.g. Kapfenstein & Tobaj). Based on these studies, the upper mantle beneath the SBVF is consists of dominantly high temperature, texturally and geochemically homogeneous protogranular spinel lherzolite. New major and trace element data from rock-forming minerals of ultramafic xenoliths, coupled with texture and deformation analysis from 12 volcanic outcrops across the SBVF, suggest that the lithospheric roots of the region are more heterogeneous than described previously. The studied xenoliths are predominantly lherzolite, amphibole is a common phase that replaces pyroxenes and spinels and proves modal metasomatism. Phlogopite coupled with apatite is also present in amphibole-rich samples. The texture of the xenoliths is usually coarse-grained and annealed with low abundance of subgrain boundaries in both olivine and pyroxenes. Olivine crystal preferred orientation (CPO) varies between the three most abundant one: [010]-fiber, orthogonal and [100]-fiber symmetry [2]. The CPO of pyroxenes is usually coherent with coeval deformation with olivine, however the CPO of amphibole is suggesting postkinematic epitaxial overgrowth on the precursor pyroxenes. According to equilibrium temperatures, the studied xenolith suite samples a broader temperature range (850-1100 °C) than the literature data, corresponding to mantle depths between 30 and 60 km, which indicates that the xenolith suite only represents the shallower part of the recent 100 km thick lithospheric mantle beneath the SBVF. The equilibrium temperatures show correlation with the varying CPO symmetries

Mantle metasomatism in the Kaapvaal Craton lithosphere: constraints on the composition of the metasomatic agent from fluid inclusions in MARID-type xenoliths

Science.gov (United States)

Konzett, J.; Krenn, K.; Hauzenberger, Ch.

2012-04-01

The emplacement of both group I and group II kimberlites in the Kaapvaal Craton of the Kimberley region in South Africa is associated with an intense metasomatic alteration of the country rocks as evidenced by a diverse suite of xenoliths sampled by the kimberlites mainly comprising metasomatized peridotites and minor MARID-type xenoliths. These are characterized by hydrous potassic silicates and LILE-HFSE-rich titanates. Because the metasomatic agent is not preserved in these rocks its composition has to be inferred from that of the metasomatic assemblages. Here we present for the first time data on fluid inclusions from two MARID-xenoliths sampled by group-I kimberlites of the Kimberley cluster. They provide direct evidence for the nature of the metasomatic fluids involved in kimberlite-related metsomatism. The xenoliths contain phlogopite+K-richterite+diopside+ilmenite±rutile±apatite±zircon. Fluid inclusions with 4-10 µm in size were found in diopside, K-richterite and zircon and contain L+V+one-to-several daughter phases. Investigations with the freezing and heating stage indicate two different chemical systems for the fluids: (1) H2O-NaCl dominant fluids found as L+V+S inclusions in zircon together with abundant needle-like apatite, rutile and phlogopite solid inclusions. The fluid inclusions in part occur along zircon host-rutile/apatite inclusion grain boundaries which indicates that the fluids were trapped during zircon growth. They contain 30-32 mass% NaCl and show a density of 0.87-0.94 g/cm3. Halos of tiny fluid inclusions, however, indicate that most if not all zircon inclusions are decrepitated during ascent from depth and/or superheating during entrainment of the xenoliths into the kimberlite. Using EMPA, enstatite and a SiO2 polymorph were identified in opened fluid inclusions exposed at the surface of polished thin sections. Because these phases were exclusively found in the fluid inclusions, they are considered daughter crystals. The enstatite

Cooling Rates of Mantle Peridotites Estimated from Lithophile Trace Element Diffusion in Orthopyroxene

Science.gov (United States)

von der Handt, A.; Hellebrand, E.; Snow, J. E.

2007-12-01

Cooling rates of ocean floor mantle rocks from mid-ocean ridges can potentially provide important information about ridge dynamics, emplacement mechanisms and mantle uplift. There are a growing number of geospeedometric methods to retrieve such cooling rates in various settings. However, few exist for typical four- phase mantle peridotites and they only cover temperatures below 800° C. The down-temperature lithophile trace element exchange between clinopyroxene (cpx) and orthopyroxene (opx) can provide such a high- temperature spinel peridotite geospeedometer. Orthopyroxenes studied by SIMS from two fresh Gakkel Ridge peridotites are zoned in all trace elements while clinopyroxenes are homogeneous. This allows the calculation of equilibrium temperatures [1]. Several profiles in opx cover a range of 1250° C (opx core) to 800° C (opx rim) and are in agreement with straightforward diffusion and closure temperature models. The systematics of REE diffusion in opx deviate from the results of a recent experimental study [2]. The data allow us to estimate diffusion systematics of 16 elements (REE and TE) and their cation distributions in orthopyroxene. The data set is internally coherent as all elements were subjected to the same extrinsic parameters. 1. Decreasing ionic radius increases REE diffusion in opx (as it does in cpx). 2. M2-site diffusion is controlled more by ionic radius than by cationic charge. 3. M1-site diffusion is controlled by both ionic radius and cationic charge. 4. M1-site diffusion is generally slower than M2-site diffusion for isovalent cations, most likely because of higher M1- site energies compared to M2-site. The advantages of this geospeedometer should be its relatively good precision, use of standard analytical methods and its coverage of the important range between solidus temperatures and 800° C. In combination with other geospeedometers it will be possible to retrieve the continuous cooling history of a mantle rock from its solidus down

Sulfur and carbon geochemistry of the Santa Elena peridotites: Comparing oceanic and continental processes during peridotite alteration

Science.gov (United States)

Schwarzenbach, Esther M.; Gill, Benjamin C.; Gazel, Esteban; Madrigal, Pilar

2016-05-01

Ultramafic rocks exposed on the continent serve as a window into oceanic and continental processes of water-peridotite interaction, so called serpentinization. In both environments there are active carbon and sulfur cycles that contain abiogenic and biogenic processes, which are eventually imprinted in the geochemical signatures of the basement rocks and the calcite and magnesite deposits associated with fluids that issue from these systems. Here, we present the carbon and sulfur geochemistry of ultramafic rocks and carbonate deposits from the Santa Elena ophiolite in Costa Rica. The aim of this study is to leverage the geochemistry of the ultramafic sequence and associated deposits to distinguish between processes that were dominant during ocean floor alteration and those dominant during low-temperature, continental water-peridotite interaction. The peridotites are variably serpentinized with total sulfur concentrations up to 877 ppm that is typically dominated by sulfide over sulfate. With the exception of one sample the ultramafic rocks are characterized by positive δ34Ssulfide (up to + 23.1‰) and δ34Ssulfate values (up to + 35.0‰). Carbon contents in the peridotites are low and are isotopically distinct from typical oceanic serpentinites. In particular, δ13C of the inorganic carbon suggests that the carbon is not derived from seawater, but rather the product of the interaction of meteoric water with the ultramafic rocks. In contrast, the sulfur isotope data from sulfide minerals in the peridotites preserve evidence for interaction with a hydrothermal fluid. Specifically, they indicate closed system abiogenic sulfate reduction suggesting that oceanic serpentinization occurred with limited input of seawater. Overall, the geochemical signatures preserve evidence for both oceanic and continental water-rock interaction with the majority of carbon (and possibly sulfate) being incorporated during continental water-rock interaction. Furthermore, there is

Petrographical, geochemical and petrological study of the xenoliths associating the basalt of (Southwest, Syria)

International Nuclear Information System (INIS)

Safarjalani, A.; Nasir, S.

1998-01-01

Alkali basalt spread northeast part of Shamah volcanic field (Southwest of Syria) belonging to the Neogene and Quaternary ages, which are coexisted with a great quantity of mafic and ultramafic xenoliths and megacrysts. Field observations and data of geochemical and petrographical studies results, for xenoliths coexisted with alkali basalt speared over the northwest part of the arabian plate (Syria) indicate availability of a proper environment where various kinds of xenoliths of lower crustal and upper mantle were formed, this indicates that these xenoliths have been formed under different thermo barometric conditions. The study of available mineral para genesis and geothermobarometrics on coexisting minerals suggests equilibration conditions, ranging between 6-8 kba for pressure and 850-920 Centigrade for temperature, and that is for xenoliths of gabbroic nature formed in the lower crustal between 20-27 km depth. With regard to the formation conditions of the xenoliths formed in the upper mantle (Pyroxenite and Lherzolite); they rang between 13.5 - 14.5 kba for pressure and 950-1060 Centigrade for temperature. (Author)

Subduction initiation and recycling of Alboran domain derived crustal components prior to the intra-crustal emplacement of mantle peridotites in the Westernmost Mediterranean: isotopic evidence from the Ronda peridotite

Science.gov (United States)

Varas-Reus, María Isabel; Garrido, Carlos J.; Bosch, Delphine; Marchesi, Claudio Claudio; Acosta-Vigil, Antonio; Hidas, Károly; Barich, Amel

2014-05-01

-Rif cordillera crustal rocks that might have been potentially subducted beneath the Alborán domain before the emplacement of Ronda peridotites. Isotopic data rules out potential crustal sources coming from pre-early Miocene Flysch Trough sediments and crustal rocks from the Blanca Unit currently underlying peridotite. Crustal rocks from the Jubrique Unit overlying the Ronda peridotite are the only crustal samples that may account for the relatively high 207Pb-208Pb/204Pb and low 206Pb/204Pb characteristic of the crustal contaminant added to the mantle source of late Cr-pyroxenites. These data strongly support Alboran geodynamic models that envisage slab roll-back as the tectonic mechanism responsible for Miocene lithospheric thinning, and provides a scenario where back-arc inversion leading to self-subduction of crustal units at the front of the Alboran wedge. REFERENCES 1. Durand-Delga, M., P. Rossi, P. Olivier, and D. Puglisi, Situation structurale et nature ophiolitique de roches basiques jurassiques associées aux flyschs maghrébins du Rif (Maroc) et de Sicile (Italie). Comptes Rendus de l'Académie des Sciences - Series IIA - Earth and Planetary Science, 2000. 331(1): p. 29-38. 2. Lenoir, X., C. Garrido, J.L. Bodinier, J.M. Dautria, and F. Gervilla, The Recrystallization Front of the Ronda Peridotite: Evidence for Melting and Thermal Erosion of Subcontinental Lithospheric Mantle beneath the Alboran Basin. Journal of Petrology, 2001. 42(1): p. 141-158. 3. Garrido, C.J., F. Gueydan, G. Booth-Rea, J. Precigout, K. Hidas, J.A. Padrón-Navarta, and C. Marchesi, Garnet lherzolite and garnet-spinel mylonite in the Ronda peridotite: Vestiges of Oligocene backarc mantle lithospheric extension in the western Mediterranean. Geology, 2011. 4. Balanyá, J.C., V. García-Dueñas, J.M. Azañón, and M. Sánchez-Gómez, Alternating contractional and extensional events in the Alpujarride nappes of the Alboran Domain (Betics, Gibraltar Arc). Tectonics, 1997. 16(2): p. 226-238. 5. Platt, J

Multiple enrichment of the Carpathian-Pannonian mantle: Pb-Sr-Nd isotope and trace element constraints

Science.gov (United States)

Rosenbaum, Jeffrey M.; Wilson, Marjorie; Downes, Hilary

1997-07-01

Pb isotope compositions of acid-leached clinopyroxene and amphibole mineral separates from spinel peridotite mantle xenoliths entrained in Tertiary-Quaternary alkali basalts from the Carpathian-Pannonian Region of eastern Europe provide important constraints on the processes of metasomatic enrichment of the mantle lithosphere in an extensional tectonic setting associated with recent subduction. Principal component analysis of Pb-Sr-Nd isotope and rare earth element compositions of the pyroxenes is used to identify the geochemical characteristics of the original lithospheric mantle protolith and a spectrum of infiltrating metasomatic agents including subduction-related aqueous fluids and silicate melts derived from a subduction-modified mantle wedge which contains a St. Helena-type (HIMU) plume component. The mantle protolith is highly depleted relative to mid-ocean ridge basalt-source mantle with Pb-Nd-Sr isotope compositions consistent with an ancient depletion event. Silicate melt infiltration into the protolith accounts for the primary variance in the Pb-Sr-Nd isotope compositions of the xenoliths and has locally generated metasomatic amphibole. Infiltration of aqueous fluids has introduced radiogenic Pb and Sr without significantly perturbing the rare earth element signature of the protolith. The Pb isotope compositions of the fluid-modified xenoliths suggest that they reacted with aqueous fluids released from a subduction zone which had equilibrated with sediment derived from an ancient basement terrain. We propose a model for mantle lithosphere evolution consistent with available textural and geochemical data for the xenolith population. The Pb-Sr-Nd isotope compositions of both alkaline mafic magmas and rare, subduction-related, calc-alkaline basaltic andesites from the region provide important constraints for the nature of the asthenospheric mantle wedge and confirm the presence of a HIMU plume component. These silicate melts contribute to the metasomatism

The semi-brittle to ductile transition in peridotite on oceanic faults: mechanisms and P-T condition

Science.gov (United States)

Prigent, C.; Warren, J. M.; Kohli, A. H.; Teyssier, C. P.

2017-12-01

Experimental and geological-petrological studies suggest that the transition from brittle faulting to ductile flow of olivine, i.e. from seismic to aseismic behavior of mantle rocks (peridotites), occurs close to 600°C. However, recent seismological studies on oceanic transform faults (TFs) and ridges have documented earthquakes to temperatures (T) up to 700-800°C. In this study, we carried out a petrological, microstructural and geochemical analysis of natural samples of peridotites dredged at 3 different oceanic TFs of the Southwest Indian Ridge: Shaka, Prince Edward and Atlantis II. We selected samples displaying variable amounts of ductile deformation (from porphyroclastic tectonites to ultramylonites) prior to serpentinization in order to characterize their relatively high-T mechanical behavior. We find that the most deformed samples record cycles of ductile and brittle deformation. Peridotite ductile flow is characterized by drastic grain size reduction and the development of (ultra)mylonitic shear zones. In these zones, a switch in olivine deformation mechanism from dislocation creep to grain-size sensitive creep is associated with dissolution/precipitation processes. Brittle deformation of these samples is evidenced by the presence of (at least centimetric) transgranular and intragranular fractures that fragment coarser grained minerals. Both kinds of fractures are filled with the same phase assemblage as in the ultramylonitic bands: olivine + amphibole ± orthopyroxene ± Al-phase (plagioclase and/or spinel) ± sulfides. The presence of amphibole indicates that this semi-brittle deformation was assisted by hydrous fluids and its composition (e.g. high concentration of chlorine) suggests that the fluids have most likely a hydrothermal origin. We interpret these fractures to have formed under fluid-assisted conditions, recording paleo-seismic activity that alternated with periods of relatively slow interseismic ductile flow. The presence of Mg

The Sidi Mohamed peridotites (Edough Massif, NE Algeria ...

Indian Academy of Sciences (India)

We suggest that the Sidi Mohamed ultramafic body was derived directly from the upper mantle and tectonically ... The aim of this paper is to determine the nature of the peridotite .... REE were enriched using the method described by. Zuleger .... Table 1. Chemical composition of the peridotites from Sidi Mohamed outcrop.

Uranium-thorium disequilibria and partitioning on melting of garnet peridotite

International Nuclear Information System (INIS)

Beattie, P.

1993-01-01

The abundances of isotopes in the 238 U decay series can be used as both tracers and chronometers of magmatic processes. In the subsolidus asthenosphere, the activity of each daughter isotope (defined as the product of its concentration and decay constant, and denoted by parentheses) is assumed to be equal to that of its parent. By contrast, ( 230 Th/ 238 U) is greater than unity in most recent mid-ocean-ridge and ocean-island basalts, implying that thorium is more incompatible (that is, it is partitioned into the melt phase more strongly) than uranium. Melting of spinel peridotite cannot produce the ( 230 Th) excesses, because measured partition coefficients for pyroxenes and olivine demonstrate that uranium is more incompatible than thorium for this rock. Here I report garnet-melt partitioning data which show that for this mineral-melt pair thorium does behave more incompatibility than uranium, thus supporting the suggestion that mid-ocean-ridge basalts (MORB) are produced by melting initiated at depths where garnet is stable. Using these data, I show that the observed ( 230 Th/ 238 U) ratios of MORB and most ocean-island basalts can be explained by slow, near-fractional melting initiated in the garnet stability field. (author)

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

Science.gov (United States)

Peslier, Anne H.; Brandon, Alan D.; Schaffer, Lillian Aurora; O'Reilly, Suzanne Yvette; Griffin, William L.; Morris, Richard V.; Graff, Trevor G.; Agresti, David G.

2014-01-01

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 (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.

The Friningen Garnet Peridotite (central Swedish Caledonides). A good example of the characteristic PTt path of a cold mantle wedge garnet peridotite

NARCIS (Netherlands)

Gilio, Mattia; Clos, Frediano; van Roermund, Herman L M|info:eu-repo/dai/nl/068882432

2015-01-01

We present pseudosections of Cr-bearing garnet peridotite that together with new mineral–chemical data allow quantification of the early PT conditions of the original lithospheric mantle assemblage (M1) of the Friningen Garnet Peridotite (FGP) located in the central/middle belt of the Seve Nappe

New calibration of Ji - Di clinopyroxene barometer for Eclogites, pyroxenites and peridotites and eclogite - pyroxenite mantle geotherms.

Science.gov (United States)

Ashchepkov, Igor; Vishnyakova, Elena

2010-05-01

.275*(1-0.17*Na/Al+0.0115*Fe/Na)*Kd^3/4*ToK/(1+Fe)* (1+5*Fe*(ToK-600)/50)-35*ln(1273/ToK)*(Al+Ti+2.5Na+1.5Fe3+)+(0.9-xx(2,8))*10+xx(2,9)/xx(2,3)* ToK /300-4*(Fe*33.2-4) -(Al-5.5)*( ToK -1300)/70-( ToK -1200)*0.015 with the second correction P=P*0.65+10+Mg*Al*( ToK -1400)/500 Where KD = Na*Mg/xAlCr*/Ca; XAlCr= Al*((T0-800)/800)**0.25+Cr-K+(4*Ti-0.0125)/(T0-600)*400+(Fe-0.21)*(T0-600)/14000 This equations reproduces the experimental pressures for 300 experimental runs with the R=0.84 and for the best set of the experimental data (Walter, 1999; Taylor ea 1998; Brey Kohler, 1990; 2009) with the E=0.95 (s=7) within the 100 kbar interval. They allow to work with the wide range of the pyroxenite compositions giving the practically coinciding PT parameters with the pressures determined for ilmenites and chromites as well as the (Brey, Kohler, 1900) pressure estimates. The PT parameters reconstructed for the mantle lithosphere beneath > 120 pipes from Yakutia , Baltica, Africa , North America and other world wide kimberlites have shown very good coincidence with the estimates from the other methods of monomineral (Nimis, Taylor, 2000; McGregor, 1974; Ashchepkov ea. 2009 ) and Gar-Opx barometers (Brey, Kohler, 1900; Nickel, Green, 1975). For the garnet and spinel xenoliths of the alkali basalts representing fertile or regenerated peridotites with high Al content of the clinopyroxenes the modified equation allows to determine the pressures together for megacrysts, pyroxeniets and peridotites using the following equation P=0.035*Kd*ToK)/(1+3.5*Fe)- 50*ln(1273/(ToK-100)*(Al+5*Na-Ti+2*Cr) -(Na-0.050)*(ToK-1200)*(Ca-0.85)/7000+5 Where KD = Na*Mg/xAlCr*/Ca; xAlCr= (Al+Si-2)*((ToK-700)/900)^0.35+Cr+Fe3-K +(4*Ti-0.0125)/(ToK-600)*700 +(Fe-0.21)*(ToK-400)/17000 This equations also very good reproduce the experimental runs in the pressure interval from 10 to 80 kbar but better to 50 kbars (R=0.92) (S=5) for 170 experimental runs (Putirka ea, 1996; Fallon ea, 1999; Taylor ea, 1998; Drapper Green

A crustal-upper mantle model for southeastern Sicily (Italy) from the integration of petrologic and geophysical data

Science.gov (United States)

Manuella, Fabio Carmelo; Brancato, Alfonso; Carbone, Serafina; Gresta, Stefano

2013-05-01

An interdisciplinary approach is proposed to investigate the structure and composition of the Permo-Triassic basement of the Hyblean Plateau and Sicily Channel. Comparisons of published data on peridotites and spinels from different geodynamic settings, and new data on Hyblean spinels, reveal the affinity of the Hyblean basement with an ultra-slow spreading oceanic lithosphere, rather than with the Africa continental plate. Similar results derive from volcanic rocks of the studied area, whose Nb/Yb vs. Th/Yb ratio hints at their affinity with the MORB-OIB array, even excluding any possible contamination with continental crust lithologies, unlike North Africa lavas. The comparison of He isotopic ratios from Hyblean Plateau and Sicily Channel highlights their similarity with values measured in fluids emitted from the Rainbow and Logatchev hydrothermal fields in Mid-Atlantic Ridge. Based on petrologic and geochemical evidence for the oceanic nature of the Permo-Triassic basement in southeastern Sicily, and the occurrence of serpentinized harzburgite xenoliths in Hyblean diatremes, the P-wave velocity model proposed for the investigated area is used to estimate lithospheric pressure, density, degree of serpentinization and magnetic susceptibility also considering both abyssal and ophiolitic serpentinites. The resulting values suggest the presence of peridotites affected by different degrees of serpentinization (35-100 vol.%) ranging to a depth of 8-19 km. As a whole, combined seismic, gravimetric and magnetic data indicate the presence of a marked anomaly at a depth of about 19 km. As a consequence, we consider the Moho discontinuity as a serpentinization front, by fixing the relative top at a depth of 19 km. Our results suggest that the oceanic lithospheric model for southeastern Sicily could be broadened to the Sicily Channel, which is possibly correlated to the adjacent Ionian oceanic basin, inferred as belonging to the Oman-Iraq-Levantine-Sicily seaway.

Millennia of magmatism recorded in crustal xenoliths from alkaline provinces in Southwest Greenland

DEFF Research Database (Denmark)

Smit, Matthijs; Waight, Tod Earle; Nielsen, Troels

2016-01-01

Neoproterozoic alkaline provinces in West Greenland: 1)Sarfartôq, which overlies Archean ultra-depleted SCLM and yielded ultra-deep mineral indicators, and 2)Sisimiut, where the SCLM is refertilized and deep xenoliths (>120km) are lacking. We focused on the rare and understudied crustal xenoliths, which preserve...

Cognate xenoliths in Mt. Etna lavas: witnesses of the high-velocity body beneath the volcano

Science.gov (United States)

Corsaro, Rosa Anna; Rotolo, Silvio Giuseppe; Cocina, Ornella; Tumbarello, Gianvito

2014-01-01

Various xenoliths have been found in lavas of the 1763 ("La Montagnola"), 2001, and 2002-03 eruptions at Mt. Etna whose petrographic evidence and mineral chemistry exclude a mantle origin and clearly point to a cognate nature. Consequently, cognate xenoliths might represent a proxy to infer the nature of the high-velocity body (HVB) imaged beneath the volcano by seismic tomography. Petrography allows us to group the cognate xenoliths as follows: i) gabbros with amphibole and amphibole-bearing mela-gabbros, ii) olivine-bearing leuco-gabbros, iii) leuco-gabbros with amphibole, and iv) Plg-rich leuco gabbros. Geobarometry estimates the crystallization pressure of the cognate xenoliths between 1.9 and 4.1 kbar. The bulk density of the cognate xenoliths varies from 2.6 to 3.0 g/cm3. P wave velocities (V P ), calculated in relation to xenolith density, range from 4.9 to 6.1 km/s. The integration of mineralogical, compositional, geobarometric data, and density-dependent V P with recent literature data on 3D V P seismic tomography enabled us to formulate the first hypothesis about the nature of the HVB which, in the depth range of 3-13 km b.s.l., is likely made of intrusive gabbroic rocks. These are believed to have formed at the "solidification front", a marginal zone that encompasses a deep region (>5 km b.s.l.) of Mt. Etna's plumbing system, within which magma crystallization takes place. The intrusive rocks were afterwards fragmented and transported as cognate xenoliths by the volatile-rich and fast-ascending magmas of the 1763 "La Montagnola", 2001 and 2002-03 eruptions.

Metamorphic reprocessing of a serpentinized carbonate-bearing peridotite after detachment from the mantle wedge: A P-T path constrained from textures and phase diagrams in the system CaO-MgO-Al 2O 3-SiO 2-CO 2-H 2O

Science.gov (United States)

Mposkos, E.; Baziotis, I.; Proyer, A.

2010-08-01

-bearing metaperidotite from Gorgona probably represents a fragment of the hydrated mantle wedge. This is indicated by the REE compositions which differ from those of ophiolitic peridotites and resemble those of spinel or garnet peridotites of sub-continental origin. The ultramafic slice was incorporated tectonically into the subduction channel, most likely by tectonic erosion in the Early Jurassic, but did not experience ultrahigh-pressure metamorphism like the nearby metapelites that exhumed along the same subduction channel.

Geochemical and petrological constraints on mantle composition of the Ohře(Eger) rift, Bohemian Massif: peridotite xenoliths from the České Středohoří Volcanic complex and northern Bohemia

Czech Academy of Sciences Publication Activity Database

Ackerman, Lukáš; Medaris Jr., G.; Špaček, P.; Ulrych, Jaromír

2015-01-01

Roč. 104, č. 8 (2015), s. 1957-1979 ISSN 1437-3254 R&D Projects: GA ČR GA205/09/1170 Institutional support: RVO:67985831 Keywords : Bohemian Massif * mantle * metasomatism * Ohře(Eger) rift * xenolith Subject RIV: DB - Geology ; Mineralogy Impact factor: 2.133, year: 2015

Sr-Nd isotope systematics of xenoliths in Cenozoic volcanic rocks from SW Japan

International Nuclear Information System (INIS)

Kagami, Hiroo; Iwata, Masatoshi; Iizumi, Shigeru; Nureki, Terukazu.

1993-01-01

Based on new and previously published Sr and Nd isotope data, we examined the petrogenetic relationship between deep crust- and upper mantle-derived xenoliths contained in Cenozoic volcanic rocks and Cretaceous-Paleogene granitoid rocks in SW Japan. The deep crust- and upper mantle-derived mafic to ultramafic xenoliths contained in Cenozoic volcanic rocks from SW Japan have comparable initial Sr and Nd isotope ratios to the Cretaceous-Paleogene granitoid rocks in their respective districts. This may suggest that these xenoliths were genetically related to the Cretaceous-Paleogene granitoid rocks in SW Japan, and that regional variations in Sr and Nd isotope ratios observed in the granitoid rocks are attributed to differences in the geochemistry of the magma sources. (author)

New evidence for the asthenospheric origin of the Cameroon Volcanic Line from 1D shear wave velocities

CSIR Research Space (South Africa)

Tokam, AP

2013-10-01

Full Text Available the mantle composition beneath Ethiopia and southern Brazil (Keranen et al., 2009; Julia et al., 2008). Many petrological studies of ultramafic orogenic massifs and ultramafic xenoliths along the CVL (mainly around Mount Cameroon and the Adamawa....N. and Oya, M. 2010. Petrological and chemical variability of peridotite xenoliths from the Cameroon Volcanic Line, West Africa: an evidence from Plume emplacement. Journal of Mineralogical and Petrological Sciences, 107, 57-69. McKenzie, D...

Micro-XANES measurements on experimental spinels and the oxidation state of vanadium in coexisting spinel and silicate melt

International Nuclear Information System (INIS)

Righter, K.; Sutton, S.R.; Newville, M.; Le, L.; Schwandt, C.S.

2006-01-01

We show that experimental spinels coexisting with silicate melt always have lower valence vanadium, and that spinels typically have 3+, whereas the coexisting melt has 4+ or 5+. Implications of these results for planetary basalts will be discussed. Spinel can be a significant host phase for V which has multiple oxidation states V 2+ , V 3+ , V 4+ or V 5+ at oxygen fugacities relevant to natural systems. The magnitude of D(V) spinel/melt is known to be a function of composition, temperature and fO 2 , but the uncertainty of the oxidation state under the range of natural conditions has made elusive a thorough understanding of D(V) spinel/melt. For example, V 3+ is likely to be stable in spinels, based on exchange with Al in experiments in the CaO-MgO-Al 2 O 3 -SiO 2 system. On the other hand, it has been argued that V 4+ will be stable across the range of natural oxygen fugacities in nature. In order to build on our previous work in more oxidized systems, we have carried out experiments at relatively reducing conditions from the FMQ buffer to 2 log fO 2 units below the IW buffer. These spinel-melt pairs, where V is present in the spinel at natural levels (∼300 ppm V), were analyzed using an electron microprobe at NASA-JSC and mi-cro-XANES at the Advanced Photon Source at Argonne National Laboratory. The new results will be used together with previous results to understand the valence of V in spinel-melt systems across 12 orders of magnitude of oxygen fugacity, and with application to natural systems.

Mantle depletion and metasomatism recorded in orthopyroxene in highly depleted peridotites

DEFF Research Database (Denmark)

Scott, James; Liu, Jingao; Pearson, D. Graham

2016-01-01

Although trace element concentrations in clinopyroxene serve as a useful tool for assessing the depletion and enrichment history of mantle peridotites, this is not applicable for peridotites in which the clinopyroxene component has been consumed (~ 25% partial melting). Orthopyroxene persists in ...

Magnetic properties of serpentinized peridotites from the Zedong ophiolite, Yarlung-Zangbo suture zone, SE Tibet

Science.gov (United States)

Li, Z.; Zheng, J.; Moskowitz, B. M.; Xiong, Q.; Liu, Q.

2017-12-01

Serpentinized mantle peridotites are widely supposed to be significant sources of the magnetic, gravity and seismic anomalies in mid-oceanic ridges, forearcs and suture zones. However, the relationship between the magnetic properties of variably serpentinized peridotites and the serpentinization process is still under debate. Ophiolite outcrops commonly comprise peridotites in different stages of serpentinization and these ophiolitic peridotites are ideal to investigate the magnetic signatures of suture zones. The Zedong ophiolite locates in the eastern part of the Yarlung-Zangbo suture zone, SE Tibet (China), and the peridotite massif represents the remnants of the Neo-Tethyan lithospheric mantle. The harzburgite and lherzolite samples show densities between 3.316 and 2.593 g cm-3, and vary from the freshest to >90% serpentinized peridotites. The magnetic susceptibility curves from room temperature to 700ºC mainly show the Curie temperatures of 585ºC for pure magnetite. The low-temperature (20-300 K) demagnetization curves show the Verwey transitions at 115-125 K, suggesting that magnetite is also the dominant remanence-carrying phase. The hysteresis data of the peridotites fall in the region of pseudo-single-domain (PSD) and follow the theoretical trends for mixtures of single domain (SD) and multidomain (MD) magnetite. The first-order reversal curve (FORC) diagrams suggest that the magnetite is dominantly interacting SD + PSD particles for S 40% serpentinized samples. The susceptibility and saturation magnetization of the Zedong peridotites range from 0.9 to 30.8 × 10‒3 (SI) and 14.1 to 1318 × 10‒3 Am2 kg‒1, respectively, and both show consistent trends with increasing degrees of serpentinization. The S serpentinization of ophiolitic peridotites, whereas the S > 40% peridotites have higher susceptibilities of 0.02-0.03 (SI) and fall in the region of abyssal peridotites. Our results suggest that the Zedong ophiolitic peridotites probably experienced a

Sulfur isotope composition of orogenic spinel lherzolite massifs from Ariege (north-eastern pyrenees, France): An ion microprobe study

Energy Technology Data Exchange (ETDEWEB)

Chaussidon, M. (Centre de Recherches Petrographiques et Geochimiques, Vandoeuvre-les-Nancy (France)); Lorand, J. (Unite associee au CNRS, Paris (France))

1990-10-01

The orogenic spinel lherzolite massifs from Ariege, which represent tectonically emplaced fragments of the sub-continental upper mantle, are composed mainly of variously depleted peridotites. These rocks are crosscut by two generations of pyroxenites. The first is made up of layered pyroxenites, which are interpreted either as crystal segregates from Triassic continental tholeiites or as subducted parts of the oceanic crust re-injected within the upper mantle. The second consists of amphibole-rich dikes separated from Cretaceous alkali basalts. Forty sulfide grains, occurring either as inclusions within silicates or as interstitial grains, were investigated by ion microprobe for their sulfur isotopic compositions. Comparison between sulfide inclusions in silicates and interstitial sulfide grains strongly suggests that serpentinization and pyrenean metamorphism had no significant effect don the {delta}{sup 34}S values. Likewise, these values are broadly independent of the degree of partial melting. The negative {delta}{sup 34}S values of the massive peridotites could represent an ancient depletion event in the upper mantle. By contrast, the positive {delta}{sup 34}S values observed in the layered pryoxenites and the amphibole-rich dikes indicate that the two parent magmas had in common a mantle source variously enriched in {sup 34}S. Therefore, the present study reveals two extreme reservoirs characterized by different {delta}{sup 34}S values in the upper mantle. This range of variations can explain most {delta}{sup 34}S values found in MORB, continental tholeiites, and alkali basalts.

Silicate melt metasomatism in the lithospheric mantle beneath SW Poland

Science.gov (United States)

Puziewicz, Jacek; Matusiak-Małek, Magdalena; Ntaflos, Theodoros; Grégoire, Michel; Kukuła, Anna

2014-05-01

The xenoliths of peridotites representing the subcontinental lithospheric mantle (SCLM) beneath SW Poland and adjacent parts of Germany occur in the Cenozoic alkaline volcanic rocks. Our study is based on detailed characterization of xenoliths occurring in 7 locations (Steinberg in Upper Lusatia, Księginki, Pilchowice, Krzeniów, Wilcza Góra, Winna Góra and Lutynia in Lower Silesia). One of the two major lithologies occurring in the xenoliths, which we call the "B" lithology, comprises peridotites (typically harzburgites) with olivine containing from 90.5 to 84.0 mole % of forsterite. The harzburgites contain no clinopyroxene or are poor in that mineral (eg. in Krzeniów the group "B" harzburgites contain pfu in ortho-, and pfu in clinopyroxene). The exception are xenoliths from Księginki, which contain pyroxenes characterised by negative correlation between mg# and Al. The REE patterns of both ortho- and clinopyroxene in the group "B" peridotites suggest equilibration with silicate melt. The rocks of "B" lithology were formed due to alkaline silicate melt percolation in the depleted peridotitic protolith. The basaltic melts formed at high pressure are usually undersaturated in both ortho- and clinopyroxene at lower pressures (Kelemen et al. 1992). Because of cooling and dissolution of ortho- and clinopyroxene the melts change their composition and become saturated in one or both of those phases. Experimental results (e.g. Tursack & Liang 2012 and references therein) show that the same refers to alkaline basaltic silicate melts and that its reactive percolation in the peridotitic host leads to decrease of Mg/(Mg+Fe) ratios of olivine and pyroxenes. Thus, the variation of relative volumes of olivine and orthopyroxene as well as the decrease of mg# of rock-forming silicates is well explained by reactive melt percolation in the peridotitic protolith consisting of high mg# olivine and pyroxenes (in the area studied by us that protolith was characterised by olivine

Low Temperature Synthesis of Magnesium Aluminate Spinel

International Nuclear Information System (INIS)

Lebedovskaya, E.G.; Gabelkov, S.V.; Litvinenko, L.M.; Logvinkov, D.S.; Mironova, A.G.; Odejchuk, M.A.; Poltavtsev, N.S.; Tarasov, R.V.

2006-01-01

The low-temperature synthesis of magnesium-aluminum spinel is carried out by a method of thermal decomposition in combined precipitated hydrates. The fine material of magnesium-aluminium spinel with average size of coherent dispersion's area 4...5 nanometers is obtained. Magnesium-aluminum spinel and initial hydrates were investigated by methods of the differential thermal analysis, the x-ray phase analysis and measurements of weight loss during the dehydration and thermal decomposition. It is established that synthesis of magnesium-aluminum spinel occurs at temperature 300 degree C by method of the x-ray phase analysis

The parent magma of xenoliths in shergottite EETA79001: Bulk and trace element composition inferred from magmatic inclusions

Science.gov (United States)

Treiman, Allan H.; Lindstrom, David J.; Martinez, Rene R.

1994-01-01

The SNC meteorites are samples of the Martian crust, so inferences about their origins and parent magmas are of wide planetologic significance. The EETA79001 shergottite, a basalt, contains xenoliths of pyroxene-olivine cumulate rocks which are possibly related to the ALHA77005 and LEW88516 SNC lherzolites. Olivines in the xenoliths contain magmatic inclusions, relics of magma trapped within the growing crystals. The magmatic inclusions allow a parent magma composition to be retrieved; it is similar to the composition reconstructed from xenolith pyroxenes by element distribution coefficients. The xenolith parent magma is similar but not identical to parent magmas for the shergottite lherzolites.

Hydration of an active shear zone: Interactions between deformation, metasomatism and magmatism - the spinel-lherzolites from the Montferrier (southern France) Oligocene basalts

International Nuclear Information System (INIS)

Cabanes, N.; Briqueu, L.

1987-01-01

Geochemical and textural investigations have been simultaneously performed on spinel-lherzolite xenoliths from the Oligo-Miocene alkali basalts of Montferrier (southern France). All the investigated samples have undergone a deformation very particular by intense shearing under high stresses (up to 1.75 kbar), low temperatures (≤900 0 C) and strain rates of about 10 -18 to 10 -15 s -1 . Mineral chemistry reveals that the Montferrier lherzolites are fragments of an undepleted relatively shallow upper mantle level located at a depth of 50 km (15 kbar). Moreover, Na and Ti enrichment in diopside would reflect a metasomatic event, also emphasized by the common occurrence of pargasite in 50-70% of the investigated samples. Crystallization of this amphibole is attributed to a hydrous infiltration which is related in time and space to the deformation. Indeed, amphibole is preferentially concentrated in strongly deformed zones and in kink-band boundaries of orthopyroxene porphyroclasts. Moreover, the grain boundaries were used by the pervasive agent to percolate into the lherzolite: significant chemical variations (increase in MgO: 15% and decrease in Al 2 O 3 : 55%) are observed within the range of 7-5 μm adjacent to the grain boundary. Finally, Sr isotopic data ( 87 Sr/ 86 Sr) demonstrate that the amphibole, i.e. the metasomatic agent, is genetically related to the host lava of the xenoliths. Thus, the hydrous silicate liquid from which the amphibole has crystallized may be an early percolation of the ascending alkali magma. (orig.)

First results from analysis of coordinated AVIRIS, TIMS, and ISM (French) data for the Ronda (Spain) and Beni Bousera (Morocco) peridotites

Science.gov (United States)

Mustard, J. F.; Hurtrez, S.; Pinet, P.; Sotin, C.

1992-01-01

Ultramafic rocks are relatively rare at the Earth's surface but constitute the vast majority of the Earth by volume. Exposures of ultramafic bodies are therefore crucial for deducing many important processes that occur in the Earth's mantle. An important science question regarding the spatial distribution, abundance, and composition of mafic minerals in ultramafic bodies that can be examined with advanced sensor data is the melting process. When a lherzolite melts, clinopyroxene (cpx) melts first and therefore variations in the modal amount of cpx remaining in the mantle are a reflection of the amount of fractional melting that has occurred. Fe goes preferentially into the melt during melting but a 20 percent batch melting (i.e. closed system) acquires less Fe relative to 20 percent fractional melting (i.e. open system). Since the strength and wavelength of diagnostic absorptions is a strong function of Fe content, it is possible to make maps of the variation in Fe:Mg ratios which can be related to the general melting process. Accurate ground-truth information about local mineralogy provides internal calibration and consistency checks. Investigations using imaging spectrometer are very complementary to field studies because advanced sensor data can provide a synoptic view of modal mineralogy and chemical composition whereas field studies focus on detailed characterization of local areas. Two excellent exposures of ultramafic lithologies are being investigated with visible to mid-infrared imaging spectrometer data: the Ronda peridotite near Ronda, Spain and the Beni Bousera ophiolitic fragment in northern Morocco. Although separated by the Alboran Sea, these bodies are thought to be related and represent fertile sub-continental mantle. The Ronda peridotite is predominantly spinel lherzolite but grades into harzburgite and shows considerable variation in major and trace element compositions. Mafic layering and dykes (i.e. olivine gabbro) are also observed. This

Magnesium isotopic composition of the Earth and chondrites

Science.gov (United States)

Teng, Fang-Zhen; Li, Wang-Ye; Ke, Shan; Marty, Bernard; Dauphas, Nicolas; Huang, Shichun; Wu, Fu-Yuan; Pourmand, Ali

2010-07-01

To constrain further the Mg isotopic composition of the Earth and chondrites, and investigate the behavior of Mg isotopes during planetary formation and magmatic processes, we report high-precision (±0.06‰ on δ 25Mg and ±0.07‰ on δ 26Mg, 2SD) analyses of Mg isotopes for (1) 47 mid-ocean ridge basalts covering global major ridge segments and spanning a broad range in latitudes, geochemical and radiogenic isotopic compositions; (2) 63 ocean island basalts from Hawaii (Kilauea, Koolau and Loihi) and French Polynesia (Society Island and Cook-Austral chain); (3) 29 peridotite xenoliths from Australia, China, France, Tanzania and USA; and (4) 38 carbonaceous, ordinary and enstatite chondrites including 9 chondrite groups (CI, CM, CO, CV, L, LL, H, EH and EL). Oceanic basalts and peridotite xenoliths have similar Mg isotopic compositions, with average values of δ 25Mg = -0.13 ± 0.05 (2SD) and δ 26Mg = -0.26 ± 0.07 (2SD) for global oceanic basalts ( n = 110) and δ 25Mg = -0.13 ± 0.03 (2SD) and δ 26Mg = -0.25 ± 0.04 (2SD) for global peridotite xenoliths ( n = 29). The identical Mg isotopic compositions in oceanic basalts and peridotites suggest that equilibrium Mg isotope fractionation during partial melting of peridotite mantle and magmatic differentiation of basaltic magma is negligible. Thirty-eight chondrites have indistinguishable Mg isotopic compositions, with δ 25Mg = -0.15 ± 0.04 (2SD) and δ 26Mg = -0.28 ± 0.06 (2SD). The constancy of Mg isotopic compositions in all major types of chondrites suggest that primary and secondary processes that affected the chemical and oxygen isotopic compositions of chondrites did not significantly fractionate Mg isotopes. Collectively, the Mg isotopic composition of the Earth's mantle, based on oceanic basalts and peridotites, is estimated to be -0.13 ± 0.04 for δ 25Mg and -0.25 ± 0.07 for δ 26Mg (2SD, n = 139). The Mg isotopic composition of the Earth, as represented by the mantle, is similar to chondrites

Processes accompanying of mantle plume emplacement into continental lithosphere: Evidence from NW Arabian plate, Western Syria

Science.gov (United States)

Sharkov, E. V.

2015-12-01

Lower crustal xenoliths occurred in the Middle Cretaceous lamprophyre diatremes in Jabel Ansaria (Western Syria) (Sharkov et al., 1992). They are represented mainly garnet granulites and eclogite-like rocks, which underwent by deformations and retrograde metamorphism, and younger fresh pegmatoid garnet-kaersutite-clinopyroxene (Al-Ti augite) rocks; mantle peridotites are absent in these populations. According to mineralogical geothermobarometers, forming of garnet-granulite suite rocks occurred under pressure 13.5-15.4 kbar (depths 45-54 kn) and temperature 965-1115oC. At the same time, among populations of mantle xenoliths in the Late Cenozoic platobasalts of the region, quite the contrary, lower crustal xenoliths are absent, however, predominated spinel lherzolites (fragments of upper cooled rim of a plume head), derived from the close depths (30-40 km: Sharkov, Bogatikov, 2015). From this follows that ancient continental crust was existed here even in the Middle Cretaceous, but in the Late Cenozoic was removed by extended mantle plume head; at that upper sialic crust was not involved in geomechanic processes, because Precambrian metamorphic rocks survived as a basement for Cambrian to Cenozoic sedimentary cover of Arabian platform. In other words, though cardinal rebuilding of deep-seated structure of the region occurred in the Late Cenozoic but it did not affect on the upper shell of the ancient lithosphere. Because composition of mantle xenolithis in basalts is practically similar worldwide, we suggest that deep-seated processes are analogous also. As emplacement of the mantle plume heads accompanied by powerful basaltic magmatism, very likely that range of lower (mafic) continental crust existence is very convenient for extension of plume heads and their adiabatic melting. If such level, because of whatever reasons, was not reached, melting was limited but appeared excess of volatile matters which led to forming of lamprophyre or even kimberlite.

Petrography and mineral chemistry of metamorphosed mantle peridotites of Nain Ophiolite (Central Iran)

OpenAIRE

Nargess Shirdashtzadeh; Ghodrat Torabi; Ramin Samadi

2017-01-01

Introduction Study of the petrology of the ophiolites as the relics of ancient oceanic lithosphere, is a powerful tool to reconstruct Earth’s history. Mantle peridotites have mostly undergone alteration and serpentinization to some extent. Thus, the relics of metamorphic signatures from the upper mantle and crustal processes from most of the peridotites have been ruined. Several recent papers deal with the mantle peridotites of Nain Ophiolite (e.g. Ghazi et al., 2010). However, no scientif...

Magmatic systems of large continental igneous provinces

Directory of Open Access Journals (Sweden)

E. Sharkov

2017-07-01

Full Text Available Large igneous provinces (LIPs formed by mantle superplume events have irreversibly changed their composition in the geological evolution of the Earth from high-Mg melts (during Archean and early Paleoproterozoic to Phanerozoic-type geochemically enriched Fe-Ti basalts and picrites at 2.3 Ga. We propose that this upheaval could be related to the change in the source and nature of the mantle superplumes of different generations. The first generation plumes were derived from the depleted mantle, whereas the second generation (thermochemical originated from the core-mantle boundary (CMB. This study mainly focuses on the second (Phanerozoic type of LIPs, as exemplified by the mid-Paleoproterozoic Jatulian–Ludicovian LIP in the Fennoscandian Shield, the Permian–Triassic Siberian LIP, and the late Cenozoic flood basalts of Syria. The latter LIP contains mantle xenoliths represented by green and black series. These xenoliths are fragments of cooled upper margins of the mantle plume heads, above zones of adiabatic melting, and provide information about composition of the plume material and processes in the plume head. Based on the previous studies on the composition of the mantle xenoliths in within-plate basalts around the world, it is inferred that the heads of the mantle (thermochemical plumes are made up of moderately depleted spinel peridotites (mainly lherzolites and geochemically-enriched intergranular fluid/melt. Further, it is presumed that the plume heads intrude the mafic lower crust and reach up to the bottom of the upper crust at depths ∼20 km. The generation of two major types of mantle-derived magmas (alkali and tholeiitic basalts was previously attributed to the processes related to different PT-parameters in the adiabatic melting zone whereas this study relates to the fluid regime in the plume heads. It is also suggested that a newly-formed melt can occur on different sides of a critical plane of silica undersaturation and can

Sr and Nd isotope composition of the metamorphic, sedimentary and ultramafic xenoliths of Lanzarote (Canary Islands): Implications for magma sources

Science.gov (United States)

Aparicio, Alfredo; Tassinari, Colombo C. G.; García, Roberto; Araña, Vicente

2010-01-01

The lavas produced by the Timanfaya eruption of 1730-1736 (Lanzarote, Canary Islands) contain a great many sedimentary and metamorphic (metasedimentary), and mafic and ultramafic plutonic xenoliths. Among the metamorphosed carbonate rocks (calc-silicate rocks [CSRs]) are monomineral rocks with forsterite or wollastonite, as well as rocks containing olivine ± orthopyroxene ± clinopyroxene ± plagioclase; their mineralogical compositions are identical to those of the mafic (gabbros) and ultramafic (dunite, wherlite and lherzolite) xenoliths. The 87Sr/ 86Sr (around 0.703) and 143Nd/ 144Nd (around 0.512) isotope ratios of the ultramafic and metasedimentary xenoliths are similar, while the 147Sm/ 144Nd ratios show crustal values (0.13-0.16) in the ultramafic xenoliths and mantle values (0.18-0.25) in some CSRs. The apparent isotopic anomaly of the metamorphic xenoliths can be explained in terms of the heat source (basaltic intrusion) inducing strong isotopic exchange ( 87Sr/ 86Sr and 143Nd/ 144Nd) between metasedimentary and basaltic rocks. Petrofabric analysis also showed a possible relationship between the ultramafic and metamorphic xenoliths.

Orphan Strontium-87 in Abyssal Peridotites: Daddy Was a Granite

Science.gov (United States)

Snow, Jonathan E.; Hart, Stanley R.; Dick, Henry J. B.

1993-12-01

The 87Sr/86Sr ratios in some bulk abyssal and alpine peridotites are too high to be binary mixtures of depleted mantle and seawater components. The apparent excess, or "orphan," 87Sr appears to be separated from its radioactive parent. Such observations were widely held to be analytical artifacts. Study of several occurrences of orphan 87Sr shows that the orphan component in abyssal peridotite is located in the alteration products of olivine and enstatite in the peridotite. The orphan 87Sr is most likely introduced by infiltration of low-temperature (<200^circC) seawater bearing suspended detrital particulates. These particulates include grains of detrital clay that are partly derived from continental (that is, granitic) sources and thus are highly radiogenic. Orphan 87Sr and other radiogenic isotopes may provide a tracer for low-temperature seawater penetrating into the oceanic crust.

Tracing alteration of mantle peridotite in the Samail ophiolite using Mg isotopes

Science.gov (United States)

de Obeso, J. C.; Kelemen, P. B.; Higgins, J. A.

2017-12-01

Magnesium is one of the main constituents of mantle peridotite ( 22.8 wt%), which has a homogeneous Mg isotopic composition (d26Mg = -0.25 ± 0.04 ‰ (2 sd) DSM3, Teng et al 2010 GCA). Mg isotopes are used as tracers of continental and oceanic weathering as they exhibit variable degrees of fractionation during alteration depending on the lithology. Here we report some of the first Mg isotopic compositions of the mantle section of the Samail ophiolite in Oman and its alteration products. The mantle section of the ophiolite is composed mainly of depleted harzburgites and dunites with mantle-like d26Mg (-0.25, -0.21 ‰). Mantle peridotite is far from equilibrium in near surface conditions leading to rapid, extensive serpentinization, carbonation and oxidation, as well as other geochemical changes. Our analyzed samples encompass most of the alteration of peridotite products observed in Oman including listvenites (completely carbonated peridotite) near the basal thrust of the ophiolite, massive magnesite veins within peridotite outcrops, and heavily altered harzburgites. Magnesite listvenites have d26Mg slightly below mantle values (-0.33, -0.33‰) while dolomite listvenites are significantly lighter (-1.46, -0.89‰). This suggests that heavy Mg isotopes were removed from the listvenites during ophiolite emplacement. Heavily altered peridotite from Wadi Fins exhibit alteration halos with drastic changes in composition. The most oxidized areas are enriched in Fe and depleted in Mg compared to the cores of the samples. These variations in Mg concentrations are complemented by a shift to heavy Mg isotopic compositions (0.74, 0.86‰), among the heaviest d26Mg values that have been reported in altered peridotite. Potential sinks for light isotopes removed from such alteration zones are massive magnesite veins with very light compositions (-3.39, -3.14‰). The fractionation of Mg isotopes observed in the mantle section of the ophiolite spans more than 50% of the known

Synthesis on spinel behaviour under irradiation

International Nuclear Information System (INIS)

Chauvin, N.; Dodane, C.; Noirot, J.; Konings, R.J.M.; Matzke, H.J.; Wiss, T.; Conrad, R.

2001-01-01

The spinel MgAl 2 O 4 is one of the materials able to be used in reactor for the transmutation of the minor actinides stemming from the back-end of the fuel cycle. It has been studied under irradiation since many years. Indeed, one of the first uses considered is to be employed as material for fusion reactors. Otherwise, it was shown that spinel presents nuclear and physico-chemical properties suitable for an utilization as nuclear inert matrix that loaded with an actinide phase constitutes a target devoted to the heterogeneous recycling in reactor. In order to improve the knowledge on spinel behaviour under irradiation, an assessment of the former studies must be done. The objective of this paper is to gather all the results of the spinel irradiations and to take out synthetic conclusion on the opportunity to use this material for the transmutation programme. (author)

Mantle strength of the San Andreas fault system and the role of mantle-crust feedbacks

NARCIS (Netherlands)

Chatzaras, V.; Tikoff, B.; Newman, J.; Withers, A.C.; Drury, M.R.

2015-01-01

In lithospheric-scale strike-slip fault zones, upper crustal strength is well constrained from borehole observations and fault rock deformation experiments, but mantle strength is less well known. Using peridotite xenoliths, we show that the upper mantle below the San Andreas fault system

Petrogenesis of pelitic xenoliths at the Babbitt CuNi deposit, Duluth Complex, Minnesota, U.S.A.

Science.gov (United States)

Ripley, Edward M.; Alawi, Jomaah A.

1988-02-01

The Babbitt deposit consists of disseminated CuFeNi sulfides found within mafic rocks of the Duluth Complex, generally near contacts with underlying metasedimentary rock types. Host rocks for the deposit include troctolites, olivine gabbros, gabbronorites, norites, and occasionally country rock hornfels. Xenoliths of country rocks are abundant in the deposit, and suggest a relationship between sulfide mineralization and country rock contamination. Country rocks in the Babbitt area include those of the middle Precambrian Biwabik Iron Formation, and both calcareous and non-calcareous pelites of the Virginia Formation. Xenoliths contain the assemblage cordierite-plagioclase-biotite-orthopyroxene, and are thought to have been derived from Virginia Formation protoliths. Comparison of protoliths and xenoliths using composition-volume, element ratio and mass-balance techniques suggests that xenoliths have been strongly depleted in volatiles, alkalis and Si. Footwall rocks show only a depletion in volatiles. Neither fluid-phase transport nor diffusion through an intergranular fluid can account for the mass of material transferred. Extensive partial melting of xenoliths, with residual enrichment of FeO, MgO and Al 2O 3, is the most viable transfer process. The lack of SiO 2 concentration gradients around xenoliths and anomalous igneous rock compositions suggest that desilicification occurred at a time when physical mixing of extracted partial melt and host magma was possible, and prior to final emplacement. Sulfide saturation may have been initiated due to Si assimilation with an auxiliary magma chamber. However, the composition of ores in the Babbitt deposit is consistent with saturation being achieved by addition of sediment-derived volatile sulfur, independent of major-element assimilation.

The diamondiferous roots of our wandering continent

International Nuclear Information System (INIS)

Gurney, J.J.

1990-01-01

Mantle xenoliths and minerals, including diamonds, found in the mainly Cretaceous kimberlites on the Kalahari craton provide evidence for the stabilization of a thick pool predominantly peridotitic continental nucleus in the Archaean. This was followed by widespread formation of lesser amounts of eclogite added to the lithosphere throughout the Proterozoic. Most diamonds were derived from the Archaean peridotite and Proterozoic eclogite and were liberated into kimberlite by xenolith disaggregation. The mantle lithosphere is heterogeneous and has undergone considerable modification by such processes as intrusive igneous activity, metasomatism of different styles, subsolidus metamorphism, deformation and probably the recycling of oceanic crust throughout much of its history. Diamond formation and preservation is similarly complex. The kimberlite-borne mantle sample provides a unique window of information about continental evolution in which the diamonds and their occasional encapsulated inclusions play a key role. 88 refs., 16 figs., 1 tab

Structural changes of manganese spinel at elevated temperatures

Energy Technology Data Exchange (ETDEWEB)

Li, Guohua; Iijima, Yukiko; Azuma, Hideto [Nishi Battery Laboratories, Sony Corporation, 4-16-1 Okata, Kanagawa 243-0021 Atsugi (Japan); Kudo, Yoshihiro [Technical Support Center, Sony Corporation, 4-16-1 Okata, Kanagawa 243-0021 Atsugi (Japan)

2002-01-01

A chemical synthesis route to Cr-doped and undoped Mn spinel was developed for the purpose of detailed structural analysis for elucidating the relationship between storage performance and structural changes at elevated temperatures. We identified a two-phase segregation in the lithium compositional range of 0.6spinel in the lithium compositional range of 0.4spinel decreased after storage at elevated temperatures. X-ray absorption fine structure (XAFS) analysis revealed that the Cr-doped samples showed less change in the local structure after storage than the undoped spinel samples. These results suggest that the Cr-doped spinel has higher structural stability at elevated temperatures than the undoped spinel.

Hydrogen and oxygen isotope constraints on hydrothermal alteration of the Trinity peridotite, Klamath Mountains, California

Science.gov (United States)

Liakhovitch, V.; Quick, J.E.; Gregory, R.T.

2005-01-01

The Trinity peridotite represents a rare opportunity to examine a relatively fertile plagioclase peridotite that was exhumed and later subjected to intrusive events in a seafloor environment, followed by its emplacement and incorporation into a continent. Over 250 stable isotopic determinations on whole rocks and minerals elucidate the hydrothermal evolution of the Trinity complex. All three serpentine polymorphs are present in the Trinity peridotite; these separate on the basis of their ??D values: antigorite, -46 serpentinization, or overprinting of earlier low-temperature seafloor serpentinization. Regionally, contours of ??D values exhibit bull's-eye patterns associated with the gabbroic plutons, with ??D maxima coinciding with the blackwall alteration at the margins on the plutons. In contrast to the hydrogen isotope behavior, oxygen isotope values of the three polymorphs are indistinguishable, spanning the range 5.3 history: (1) lithospheric emplacement and cooling of the peridotite in an oceanic environment ??? 472 Ma; (2) intrusion of gabbroic plutons into cold peridotite in an arc environment between 435 and 404 Ma; and finally (3) intrusion of felsic plutons between 171 and 127 Ma, long after the peridotite was incorporated into the continental crust. Copyright ?? 2005 by V. H. Winston & Son, Inc. All rights reserved.

Retrogressive hydration of calc-silicate xenoliths in the eastern Bushveld complex: evidence for late magmatic fluid movement

Science.gov (United States)

Wallmach, T.; Hatton, C. J.; De Waal, S. A.; Gibson, R. L.

1995-11-01

Two calc-silicate xenoliths in the Upper Zone of the Bushveld complex contain mineral assemblages which permit delineation of the metamorphic path followed after incorporation of the xenoliths into the magma. Peak metamorphism in these xenoliths occurred at T=1100-1200°C and P <1.5 kbar. Retrograde metamorphism, probably coinciding with the late magmatic stage, is characterized by the breakdown of akermanite to monticellite and wollastonite at 700°C and the growth of vesuvianite from melilite. The latter implies that water-rich fluids (X CO 2 <0.2) were present and probably circulating through the cooling magmatic pile. In contrast, calc-silicate xenoliths within the lower zones of the Bushveld complex, namely in the Marginal and Critical Zones, also contain melilite, monticellite and additional periclase with only rare development of vesuvianite. This suggests that the Upper Zone cumulate pile was much 'wetter' in the late-magmatic stage than the earlier-formed Critical and Marginal Zone cumulate piles.

Negative CO2 emissions via subsurface mineral carbonation in fractured peridotite

Science.gov (United States)

Kelemen, P. B.; Matter, J.

2014-12-01

Uptake of CO2 from surface water via mineral carbonation in peridotite can be engineered to achieve negative CO2 emissions. Reaction with peridotite, e.g., CO2 + olivine (A), serpentine (B) and brucite (C), forms inert, non-toxic, solid carbonates such as magnesite. Experimental studies show that A can be 80% complete in a few hours with 30 micron powders and elevated P(CO2) [1,2,3]. B is slower, but in natural systems the rate of B+C is significant [4]. Methods for capture of dilute CO2 via mineral carbonation [4,5,6,7] are not well known, though CO2 storage via mineral carbonation has been discussed for decades [8,9]. Where crushed peridotite is available, as in mine tailings, increased air or water flow could enhance CO2 uptake at a reasonable cost [4,5]. Here we focus on enhancing subsurface CO2 uptake from surface water flowing in fractured peridotite, in systems driven by thermal convection such as geothermal power plants. Return of depleted water to the surface would draw down CO2 from the air [6,7]. CO2 uptake from water, rate limited by flow in input and output wells, could exceed 1000 tons CO2/yr [7]. If well costs minus power sales were 0.1M to 1M and each system lasts 10 years this costs oil industry. Uptake of 1 Gt CO2/yr at 1000 t/well/yr requires 1M wells, comparable to the number of producing oil and gas wells in the USA. Subsurface CO2 uptake could first be applied in coastal, sub-seafloor peridotite with onshore drilling. Sub-seafloor peridotite is extensive off Oman, New Caledonia and Papua New Guinea, with smaller amounts off Spain, Morocco, USA, etc. This would be a regional contribution, used in parallel with other methods elsewhere. To achieve larger scale is conceivable. There is a giant mass of seafloor peridotite along slow-spreading mid-ocean ridges. Could robotic drills enhance CO2 uptake at a reasonable cost, while fabric chimneys transport CO2-depleted water to the sea surface? Does anyone know James Cameron's phone number? [1] O

Evolution of the volcanic plumbing systemof Alicudi (Aeolian Islands - Italy: evidence from fluid and melt inclusionsin quartz xenoliths

Directory of Open Access Journals (Sweden)

A. Peccerillo

2004-06-01

Full Text Available Quartz-rich xenoliths in lavas (basalts to andesites; 90-30 ka from Alicudi contain abundant melt and fluid inclusions. Two generations of CO2-rich fluid inclusions are present in quartz-rich xenolith grains: early (Type I inclusions related to partial melting of the host xenoliths, and late Type II inclusions related to the fluid trapping during xenolith ascent. Homogenisation temperatures of fluid inclusions correspond to two density intervals: 0.93-0.68 g/cm3 (Type I and 0.47-0.26 g/cm3 (Type II. Early Type I fluid inclusions indicate trapping pressures around 6 kbar, which are representative for the levels of partial melting of crustal rocks and xenolith formation. Late Type II fluid inclusions show lower trapping pressures, between 1.7 kbar and 0.2 kbar, indicative for shallow magma rest and accumulation during ascent to the surface. Data suggest the presence of two magma reservoirs: the first is located at lower crustal depths (about 24 km, site of fractional crystallization, mixing with source derived magma, and various degrees of crustal assimilation. The second magma reservoir is located at shallow crustal depths (about 6 km, the site where magma rested for a short time before erupting.

The helium flux from the continents and ubiquity of low-3He/4He recycled crust and lithosphere

Science.gov (United States)

Day, James M. D.; Barry, Peter H.; Hilton, David R.; Burgess, Ray; Pearson, D. Graham; Taylor, Lawrence A.

2015-03-01

New helium isotope and trace-element abundance data are reported for pyroxenites and eclogites from South Africa, Siberia, and the Beni Bousera Massif, Morocco that are widely interpreted to form from recycled oceanic crustal protoliths. The first He isotope data are also presented for Archaean peridotites from the Kaapvaal (South Africa), Slave (Canada), and Siberian cratons, along with recently emplaced off-craton peridotite xenoliths from Kilbourne Hole, San Carlos (USA) and Vitim (Siberia), to complement existing 3He/4He values obtained for continental and oceanic peridotites. Helium isotope compositions of peridotite xenoliths vary from 7.3 to 9.6 RA in recently (volcanics that contain a contribution from asthenospheric sources. Using the new He isotope data for cratonic peridotites and assuming that significant portions (>50%) of the Archaean and Proterozoic continental lithospheric mantle are stable and unaffected by melt or fluid infiltration on geological timescales (>0.1 Ga), and that U and Th contents vary between cratonic lithosphere and non-cratonic lithosphere, calculations yield a 3He flux of 0.25-2.2 atoms/s/cm2 for the continental lithospheric mantle. These estimates differ by a factor of ten from non-cratonic lithospheric mantle and are closer to the observed 3He flux from the continents (<1 atoms/s/cm2). Pyroxenites and eclogites from the continental regions are all characterized by 3He/4He (0.03-5.6 RA) less than the depleted upper mantle, and relatively high U and Th contents. Together with oceanic and continental lithospheric peridotites, these materials represent reservoirs with low time-integrated 3He/(U + Th) in the mantle. Pyroxenites and eclogites are also characterized by higher Fe/Mg, more radiogenic Os-Pb isotope compositions, and more variable δ18O values (∼3‰ to 7‰), compared with peridotitic mantle. These xenoliths are widely interpreted to be the metamorphic/metasomatic equivalents of recycled oceanic crustal protoliths. The

Invasion of Hydrous Fluids Predates Kimberlite Formation

Science.gov (United States)

Kopylova, M. G.; Wang, Q.; Smith, E. M.

2017-12-01

Petrological observations on diamonds and peridotite xenoliths in kimberlites point towards an influx of hydrous metasomatic fluids shortly predating kimberlite formation. Diamonds may grow at different times within the same segment of the cratonic mantle, and diamonds that form shortly before (diamonds typically contain 10-25 wt.% water in fluid inclusions, while older octahedrally-grown diamonds host "dry" N2-CO2 fluids. Our recent studies of fluids in diamond now show that many different kinds of diamonds can contain fluid inclusions. Specifically, we found a new way to observe and analyze fluids in octahedrally-grown, non-fibrous diamonds by examining healed fractures. This is a new textural context for fluid inclusions that reveals a valuable physical record of infiltrating mantle fluids, that postdate diamond growth, but equilibrate within the diamond stability field at depths beyond 150 km. Another sign of the aqueous fluids influx is the formation of distinct peridotite textures shortly predating the kimberlite. Kimberlites entrain peridotite xenoliths with several types of textures: older coarse metamorphic textures and younger, sheared textures. The preserved contrast in grain sizes between porphyroclasts and neoblasts in sheared peridotites constrain the maximum duration of annealing. Experimental estimates of the annealing time vary from 7x107 sec (2 years) to 106 years (1 My) depending on olivine hydration, strain rate, pressure, temperature and, ultimately, the annealing mechanism. Kimberlite sampling of sheared peridotites from the lithosphere- asthenosphere boundary (LAB) implies their formation no earlier than 1 My prior to the kimberlite ascent. Water contents of olivine measured by FTIR spectrometry using polarized light demonstrated contrasting hydration of coarse and sheared samples. Olivine from sheared peridotite samples has the average water content of 78±3 ppm, in contrast to the less hydrated coarse peridotites (33±6 ppm). LAB hydration

Spinel-structured surface layers for facile Li ion transport and improved chemical stability of lithium manganese oxide spinel

Energy Technology Data Exchange (ETDEWEB)

Lee, Hae Ri [Center for Energy Convergence Research, Korea Institute of Science Technology, Hwarang-ro 14-gil 5, Seongbuk-gu, Seoul 136-791 (Korea, Republic of); Department of Chemical and Biological Engineering, Korea University, 145, Anam-ro, Seongbuk-gu, Seoul 136-701 (Korea, Republic of); Seo, Hyo Ree; Lee, Boeun; Cho, Byung Won [Center for Energy Convergence Research, Korea Institute of Science Technology, Hwarang-ro 14-gil 5, Seongbuk-gu, Seoul 136-791 (Korea, Republic of); Lee, Kwan-Young [Department of Chemical and Biological Engineering, Korea University, 145, Anam-ro, Seongbuk-gu, Seoul 136-701 (Korea, Republic of); Oh, Si Hyoung, E-mail: sho74@kist.re.kr [Center for Energy Convergence Research, Korea Institute of Science Technology, Hwarang-ro 14-gil 5, Seongbuk-gu, Seoul 136-791 (Korea, Republic of)

2017-01-15

Graphical abstract: Strategically-designed spinel-structured nano-scale surface layer, LiM{sub x}Mn{sup IV}{sub 1−x}O{sub 4}, featuring a high Li{sup +} ion conductivity and a good chemical stability was applied on Al-doped LiMn{sub 2}O{sub 4} spinel for the drastic improvement of the electrochemical performance at the elevated temperature as a promising cathode material for lithium rechargeable batteries. - Highlights: • Spinel-structured surface layer with a high Li-ion conductivity and a good chemical stability was prepared. • Simple wet process was developed to apply nano-scale surface layer on aluminum doped lithium manganese oxide spinel. • The properties of nano-scale surface layer were characterized by analytical tools including GITT, HR-TEM and XAS. • Materials with surface coating layer exhibit an excellent electrochemical performance at the elevated temperature. - Abstract: Li-ion conducting spinel-structured oxide layer with a manganese oxidation state close to being tetravalent was prepared on aluminum-doped lithium manganese oxide spinel for improving the electrochemical performances at the elevated temperatures. This nanoscale surface layer provides a good ionic conduction path for lithium ion transport to the core and also serves as an excellent chemical barrier for protecting the high-capacity core material from manganese dissolution into the electrolyte. In this work, a simple wet process was employed to prepare thin LiAlMnO{sub 4} and LiMg{sub 0.5}Mn{sub 1.5}O{sub 4} layers on the surface of LiAl{sub 0.1}Mn{sub 1.9}O{sub 4}. X-ray absorption studies revealed an oxidation state close to tetravalent manganese on the surface layer of coated materials. Materials with these surface coating layers exhibited excellent capacity retentions superior to the bare material, without undermining the lithium ion transport characteristics and the high rate performances.

Ceramic compositions based on nano forsterite/nano magnesium aluminate spinel powders

International Nuclear Information System (INIS)

Khattab, R.M.; Wahsh, M.M.S.; Khalil, N.M.

2015-01-01

According to the wide applications in the field of chemical and engineering industries, forsterite (Mg_2SiO_4)/spinel (MgAl_2O_4) ceramic compositions were the matter of interest of several research works during the last three decades. This work aims at preparation and characterization of improved ceramic bodies based on forsterite and spinel nano powders through controlling the forsterite and spinel contents in the prepared mixes. These prepared ceramic compositions have been investigated through measuring the densification parameters, cold crushing strength as well as volume resistively. Nano spinel was added from 0 to 30 mass% on expense of nano forsterite matrix and fired at 1550 °C for 2 h. The phase composition of the fired samples was examined using x-ray diffraction (XRD) technique. The microstructure of some selected samples was shown using scanning electron microscope (SEM). A pronounced improvement in the sintering, mechanical properties and volume resistively were achieved with increasing of nano spinel addition up to 15 mass%. This is due to the improvement in the matrix of the prepared forsterite/spinel bodies as a result of well distribution of spinel in the forsterite matrix as depicted by SEM analysis. - Highlights: • Ceramic compositions based on nano forsterite/nano-MgAl_2O_4 spinel were synthesized. • CCS was improved (333.78 MPa) through 15 mass% of nano-MgAl_2O_4 spinel addition. • Volume resistivity was enhanced to 203*10"1"3 Ohm cm with 15 mass% of spinel addition. • Beyond 15 mass% spinel, CCS and volume resistivity were decreased.

The evolution and ascent paths of mantle xenolith-bearing magma: Observations and insights from Cenozoic basalts in Southeast China

Science.gov (United States)

Sun, Pu; Niu, Yaoling; Guo, Pengyuan; Cui, Huixia; Ye, Lei; Liu, Jinju

2018-06-01

Studies have shown that mantle xenolith-bearing magmas must ascend rapidly to carry mantle xenoliths to the surface. It has thus been inferred inadvertently that such rapid ascending melt must have undergone little crystallization or evolution. However, this inference is apparently inconsistent with the widespread observation that xenolith-bearing alkali basalts are variably evolved with Mg# ≤72. In this paper, we discuss this important, yet overlooked, petrological problem and offer new perspectives with evidence. We analyzed the Cenozoic mantle xenolith-bearing alkali basalts from several locations in Southeast China that have experienced varying degrees of fractional crystallization (Mg# = 48-67). The variably evolved composition of host alkali basalts is not in contradiction with rapid ascent, but rather reflects inevitability of crystallization during ascent. Thermometry calculations for clinopyroxene (Cpx) megacrysts give equilibrium temperatures of 1238-1390 °C, which is consistent with the effect of conductive cooling and melt crystallization during ascent because TMelt > TLithosphere. The equilibrium pressure (18-27 kbar) of these Cpx megacrysts suggests that the crystallization takes place under lithospheric mantle conditions. The host melt must have experienced limited low-pressure residence in the shallower levels of lithospheric mantle and crust. This is in fact consistent with the rapid ascent of the host melt to bring mantle xenoliths to the surface.

Asphaltene-bearing mantle xenoliths from Hyblean diatremes, Sicily

Science.gov (United States)

Scirè, Salvatore; Ciliberto, Enrico; Crisafulli, Carmelo; Scribano, Vittorio; Bellatreccia, Fabio; Ventura, Giancarlo Della

2011-08-01

Microscopic blebs of sulfur-bearing organic matter (OM) commonly occur between the secondary calcite grains and fibrous phyllosilicates in extensively serpentinized and carbonated mantle-derived ultramafic xenoliths from Hyblean nephelinite diatremes, Sicily, Italy. Rarely, coarse bituminous patches give the rock a blackish color. Micro Fourier transform infrared spectra (μ-FTIR) point to asphaltene-like structures in the OM, due to partially condensed aromatic rings with aliphatic tails consisting of a few C atoms. X-ray photoelectron spectroscopy (XPS) analysis indicates the occurrence of minor S═O (either sulphonyl or sulphoxide) functional groups in the OM. Solubility tests in toluene, thermo-gravimetric (TGA) and differential thermal (DTA) analyses confirm the presence of asphaltene structures. It is proposed that asphaltenes derive from the in situ aromatization (with decrease in H/C ratio) of previous light aliphatic hydrocarbons. Field evidence excludes that hydrocarbon from an external source percolated through the xenolith bearing tuff-breccia. The discriminating presence of hydrocarbon in a particular type of xenolith only and the lack of hydrocarbon in the host breccia matrix, are also inconsistent with an interaction between the ascending eruptive system and a supposed deep-seated oil reservoir. Assuming that the Hyblean unexposed basement consists of mantle ultramafics and mafic intrusive rocks having hosted an early abyssal-type hydrothermal system, one can put forward the hypothesis that the hydrocarbon production was related to hydrothermal activity in a serpentinite system. Although a bacteriogenesis or thermogenesis cannot be ruled out, the coexisting serpentine, Ni-Fe ores and hydrocarbon strongly suggest a Fischer-Tropsch-type (FTT) synthesis. Subsequent variations in the chemical and physical conditions of the system, for example an increase in the water/rock ratio, gave rise to partial oxidation and late carbonation of the serpentinite

Two types of gabbroic xenoliths from rhyolite dominated Niijima volcano, northern part of Izu-Bonin arc: petrological and geochemical constraints

Science.gov (United States)

Arakawa, Yoji; Endo, Daisuke; Ikehata, Kei; Oshika, Junya; Shinmura, Taro; Mori, Yasushi

2017-03-01

We examined the petrography, petrology, and geochemistry of two types of gabbroic xenoliths (A- and B-type xenoliths) in olivine basalt and biotite rhyolite units among the dominantly rhyolitic rocks in Niijima volcano, northern Izu-Bonin volcanic arc, central Japan. A-type gabbroic xenoliths consisting of plagioclase, clinopyroxene, and orthopyroxene with an adcumulate texture were found in both olivine basalt and biotite rhyolite units, and B-type gabbroic xenoliths consisting of plagioclase and amphibole with an orthocumulate texture were found only in biotite rhyolite units. Geothermal- and barometricmodelling based on mineral chemistry indicated that the A-type gabbro formed at higher temperatures (899-955°C) and pressures (3.6-5.9 kbar) than the B-type gabbro (687-824°C and 0.8-3.6 kbar). These findings and whole-rock chemistry suggest different parental magmas for the two types of gabbro. The A-type gabbro was likely formed from basaltic magma, whereas the B-type gabbro was likely formed from an intermediate (andesitic) magma. The gabbroic xenoliths in erupted products at Niijima volcano indicate the presence of mafic to intermediate cumulate bodies of different origins at relatively shallower levels beneath the dominantly rhyolitic volcano.

Fragments of deeper parts of the hanging wall mantle preserved as orogenic peridotites in the central belt of the Seve Nappe Complex, Sweden

Science.gov (United States)

Clos, Frediano; Gilio, Mattia; van Roermund, Herman L. M.

2014-04-01

Formation conditions of olivine microstructures are investigated in the Kittelfjäll spinel peridotite (KSP), a fragment of lithospheric mantle which occurs as an isolated body within high grade metamorphic crustal rocks of the Seve Nappe Complex (SNC), southern Västerbotten, central Sweden. The KSP is an orogenic peridotite containing a well developed penetrative compositional layering, defined by highly depleted dunite with olivine Mg# (100 × Mg/Mg + Fe) of 92.0-93.5 and harzburgite with lower Mg# (91.0-92.5). Dunite is characterized by three contrasting olivine microstructures formed in response to different tectonometamorphic events: Coarse-grained, highly strained olivine porphyroclasts (M1) up to 20 cm long are surrounded by dynamically recrystallized olivine grains (M2) defining a characteristic olivine "foam" microstructure (grain size: 200-2000 μm). An olivine "mortar" (M3) microstructure (10-50 μm) forms a penetrative fabric element only in strongly localized, cm-to-m sized shear zones that crosscut earlier structures/foliations. Olivine fabric analysis in synergy, with mineralogical and chemical analyses, reveals that the KSP body represents old, possibly Archean, sub-continental lithospheric mantle that was crustally emplaced into the Caledonian tectonic edifice from the hanging wall mantle during exhumation of the subducted Seve Nappe Complex (Jämtlandian orogeny ~ 454 Ma). Olivine porphyroclasts (M1) grew at high temperature during dominant isobaric cooling after extensive polybaric melt extraction (> 40%) and subsequent refertilization. The onset of the early Caledonian deformation is interpreted to be related to the crustal emplacement of the KSP during eduction of the SNC. This phase is characterized by the development of the olivine M2 foam microstructure, formed at 650-830 °C/1-2 GPa by dislocation creep processes producing an E-type CPO's by the operation of the [100](001) and subordinate [001](100) slip systems with operating flow stress

Mineral compositions of plutonic rocks from the Lewis Hills massif, Bay of Islands ophiolite

Science.gov (United States)

Smith, Susan E.; Elthon, Don

1988-01-01

Mineral compositions of residual and cumulate rocks from the Lewis Hills massif of the Bay of Islands ophiolite complex are reported and interpreted in the context of magnetic processes involved in the geochemical evolution of spatially associated diabase dikes. The mineral compositions reflect greater degrees of partial melting than most abyssal peridotites do and appear to represent the most depleted end of abyssal peridotite compositions. Subsolidus equilibration between Cr-Al spinal and olivine generally has occurred at temperatures of 700 to 900 C. The spinel variations agree with the overall fractionation of basaltic magmas producing spinels with progressively lower Cr numbers. The compositions of clinopyroxenes suggest that the fractionation of two different magma series produced the various cumulate rocks.

Magnetic behavior of the oxide spinels:

Indian Academy of Sciences (India)

Magnetic behavior of the oxide spinels: Li0.5Fe2.5−2xAlxCrxO4. U N TRIVEDI, K B MODI and H H JOSHI. Department of Physics, Saurashtra University, Rajkot 360 005, India. Abstract. In order to study the effect of substitution of Fe3+ by Al3+ and Cr3+ in Li0.5Fe2.5O4 on its structural and magnetic properties, the spinel ...

Petrology and Geochemistry of Serpentinized Peridotites from a Bonin Fore-arc Seamount

Science.gov (United States)

Tian, L.; Tuoyu, W.; Dong, Y. H.; Gao, J.; Wu, S.

2016-12-01

Serpentinites, which contain up to 13 wt.% of water, are an important reservoir for chemical recycling in subduction zones. During the last two decades, many observations documented the occurrence of fore-arc mantle serpentinites in different locations. Here, we present petrology and whole rock chemistry for serpentinized peridotites dredged from the Hahajima Seamount, which is located 20-60 km west of the junction of the Bonin Trench and the Mariana Trench. Combined with published geochemical data of serpentinites from the Torishima Seamount, Conical Seamount and South Chamorro Seamount in the Izu-Bonin-Mariana fore-arc region, it will allow us to better understand the average composition of serpentinized fore-arc mantle overlying the subducting slab and the role of serpentinized mantle playing in the subduction zone geochemical cycle. The studied ultramafic rocks from the Hahajima Seamount are extensively serpentinized and hydrated (73 to 83%), with loss of ignition values ranging between 13 and 15 wt.%. Our results show that the serpentinized peridotites have Mg number from 88 to 90, and the average MgO/SiO2 is 0.93. The average Al2O3 (0.48 wt.%) and CaO (0.23 wt.%) contents are very low, consistent with low clinopyroxene abundances, and the overall depleted character of the mantle harzburgite protoliths. The serpentinized peridotites from the Hahajima Seamount exhibit similar "U" shape rare earth element (REE) patterns ([La/Sm]N = 3.1-3.6), at higher overall abundances, to the Conical and South Chamorro Seamount suites. One exceptional sample shows the similar REE pattern as serpentinized peridotites from the Torishima Seamount, with depleted light REE concentration ([La/Sm]N =0.7). All the serpentinized peridotites from these four fore-arc seamounts show strong enrichment in fluid-mobile and lithophile elements (U, Pb, Sr and Li). The geochemical signature of the serpentinized peridotites from the seamounts in the Izu-Bonin-Mariana fore-arc region could be

Synthesis of magnesium aluminate spinel by periclase and alumina chlorination

International Nuclear Information System (INIS)

Orosco, Pablo; Barbosa, Lucía; Ruiz, María del Carmen

2014-01-01

Highlights: • Use of chlorination for the synthesis of magnesium aluminate spinel. • The reagents used were alumina, periclase and chlorine. • Isothermal and non-isothermal assays were performed in air and Cl 2 –N 2 flows. • The chlorination produced magnesium aluminate spinel at 700 °C. • Selectivity of the chlorination reaction to obtain spinel is very high. - Abstract: A pyrometallurgical route for the synthesis of magnesium aluminate spinel by thermal treatment of a mechanical mixture containing 29 wt% MgO (periclase) and 71 wt% Al 2 O 3 (alumina) in chlorine atmosphere was developed and the results were compared with those obtained by calcining the same mixture of oxides in air atmosphere. Isothermal and non-isothermal assays were performed in an experimental piece of equipment adapted to work in corrosive atmospheres. Both reagents and products were analyzed by differential thermal analysis (DTA), X-ray diffraction (XRD) and X-ray fluorescence (XRF). Thermal treatment in Cl 2 atmosphere of the MgO–Al 2 O 3 mixture produces magnesium aluminate spinel at 700 °C, while in air, magnesium spinel is generated at 930 °C. The synthesis reaction of magnesium aluminate spinel was complete at 800 °C

Mineral chemistry and geochemistry of ophiolitic metaultramafics from Um Halham and Fawakhir, Central Eastern Desert, Egypt

Science.gov (United States)

Abdel-Karim, Abdel-Aal M.; Ali, Shehata; El-Shafei, Shaimaa A.

2018-03-01

This study is focused on ophiolitic metaultramafics from Um Halham and Fawakhir, Central Eastern Desert of Egypt. The rocks include serpentinized peridotites, serpentinites together with talc- and quartz-carbonates. The primary spinel relict is Al-chromite [Cr# > 60], which is replaced by Cr-magnetite during metamorphism. The high Cr# of Al-chromites resembles supra-subduction zone (SSZ) peridotites and suggests derivation from the deeper portion of the mantle section with boninitic affinity. These mantle rocks equilibrated with boninitic melt have been generated by high melting degrees. The estimated melting degrees ( 19-24%) lie within the range of SSZ peridotites. The high Cr# of spinel and Fo content of olivine together with the narrow compositional range suggest a mantle residual origin. Serpentinized peridotite and serpentinites have low Al2O3/SiO2 ratios (mostly serpentinization process. Moreover, they have very low Nb, Ta, Zr and Hf concentrations along with sub-chondritic Nb/Ta (0.3-16) and Zr/Hf (mostly 1-20) ratios further confirming that their mantle source was depleted by earlier melting extraction event. The high chondrite normalized (La/Sm)N ratios (average 10) reflect input of subduction-related slab melts/fluids into their mantle source.

Two types of gabbroic xenoliths from rhyolite dominated Niijima volcano, northern part of Izu-Bonin arc: petrological and geochemical constraints

Directory of Open Access Journals (Sweden)

Arakawa Yoji

2017-03-01

Full Text Available We examined the petrography, petrology, and geochemistry of two types of gabbroic xenoliths (A- and B-type xenoliths in olivine basalt and biotite rhyolite units among the dominantly rhyolitic rocks in Niijima volcano, northern Izu-Bonin volcanic arc, central Japan. A-type gabbroic xenoliths consisting of plagioclase, clinopyroxene, and orthopyroxene with an adcumulate texture were found in both olivine basalt and biotite rhyolite units, and B-type gabbroic xenoliths consisting of plagioclase and amphibole with an orthocumulate texture were found only in biotite rhyolite units. Geothermal- and barometricmodelling based on mineral chemistry indicated that the A-type gabbro formed at higher temperatures (899–955°C and pressures (3.6–5.9 kbar than the B-type gabbro (687–824°C and 0.8–3.6 kbar. These findings and whole-rock chemistry suggest different parental magmas for the two types of gabbro. The A-type gabbro was likely formed from basaltic magma, whereas the B-type gabbro was likely formed from an intermediate (andesitic magma. The gabbroic xenoliths in erupted products at Niijima volcano indicate the presence of mafic to intermediate cumulate bodies of different origins at relatively shallower levels beneath the dominantly rhyolitic volcano.

Empirical constraints on partitioning of platinum group elements between Cr-spinel and primitive terrestrial magmas

Science.gov (United States)

Park, Jung-Woo; Kamenetsky, Vadim; Campbell, Ian; Park, Gyuseung; Hanski, Eero; Pushkarev, Evgeny

2017-11-01

Recent experimental studies and in situ LA-ICP-MS analysis on natural Cr-spinel have shown that Rh and IPGEs (Ir-group platinum group elements: Ru, Ir, Os) are enriched in the lattice of Cr-spinel. However, the factors controlling the partitioning behaviour of these elements are not well constrained. In this study, we report the Rh, IPGE, and trace element contents in primitive Cr-spinel, measured by LA-ICP-MS, from nine volcanic suites covering various tectonic settings including island arc picrites, boninites, large igneous province picrites and mid-ocean ridge basalts. The aim is to understand the factors controlling the enrichment of Rh and IPGEs in Cr-spinels, to estimate empirical partition coefficients between Cr-spinel and silicate melts, and to investigate the role of Cr-spinel fractional crystallization on the PGE geochemistry of primitive magmas during the early stages of fractional crystallization. There are systematic differences in trace elements, Rh and IPGEs in Cr-spinels from arc-related magmas (Arc Group Cr-spinel), intraplate magmas (Intraplate Group Cr-spinel), and mid-ocean ridge magmas (MORB Group Cr-spinel). Arc Group Cr-spinels are systematically enriched in Sc, Co and Mn and depleted in Ni compared to the MORB Group Cr-spinels. Intraplate Group Cr-spinels are distinguished from the Arc Group Cr-spinels by their high Ni contents. Both the Arc and Intraplate Group Cr-spinels have total Rh and IPGE contents of 22-689 ppb whereas the MORB Group Cr-spinels are depleted in Rh and IPGE (total time-resolved spectra of LA-ICP-MS data for Cr-spinels mostly show constant count rates for trace element and Rh and IPGEs, suggesting homogeneous distribution of these elements in Cr-spinels. The PGE spikes observed in several Cr-spinels were interpreted to be PGE-bearing mineral inclusions and excluded from calculating the PGE contents of the Cr-spinels. On primitive mantle normalized diagrams the Arc Group Cr-spinels are characterized by a fractionated

Rapid Grain Size Reduction in the Upper Mantle at a Plate Boundary

Science.gov (United States)

Kidder, S. B.; Scott, J.; Prior, D. J.; Lubicich, E. J.

2017-12-01

A few spinel peridotite xenoliths found near the Alpine Fault, New Zealand, exhibit a mylonitic texture and, locally, an extremely fine 30 micron grain size. The harzburgite xenoliths were emplaced in a 200 km-long elongate dike zone interpreted as a gigantic tension fracture or Reidel shear associated with Alpine Fault initiation 25 Ma. The presence of thin ( 1 mm) ultramylonite zones with px-ol phase mixing and fine grain sizes, minimal crustal-scale strain associated with the dike swarm, and the absence of mylonites at four of the five xenolith localities associated with the dike swarm indicate that upper mantle deformation was highly localized. Strings of small, recrystallized grains (planes in 3D) are found in the interiors of olivine porphyroclasts. In some cases, bands 1-2 grains thick are traced from the edges of olivine grains and terminate in their interiors. Thicker zones of recrystallized grains are also observed crossing olivine porphyroclasts without apparent offset of the unrecrystallized remnants of the porphyroclasts. We suggest a brittle-plastic origin for these features since the traditional recrystallization mechanisms associated with dislocation creep require much more strain than occurred within these porphyroclasts. Analogous microstructures in quartz and feldspar in mid-crust deformation zones are attributed to brittle-plastic processes. We hypothesize that such fine-grained zones were the precursors of the observed, higher-strain ultramylonite zones. Given the size of the new grains preserved in the porphyroclasts ( 100 micron) and a moho temperature > 650°C, grain growth calculations indicate that the observed brittle-plastic deformation occurred <10,000 yrs. prior to eruption. It is likely then that either brittle-plastic deformation was coeval with the ductile shearing occurring in the ultramylonite bands, or possibly, if deformation can be separated into brittle-plastic (early) and ductile (later) phases, that the entire localization

Geochronology and geochemistry of deep-seated crustal xenoliths in the northern North China Craton: Implications for the evolution and structure of the lower crust

Science.gov (United States)

Su, Yuping; Zheng, Jianping; Griffin, William L.; Huang, Yan; Wei, Ying; Ping, Xianquan

2017-11-01

The age and composition of the lower crust are critical in understanding the processes of continental formation and evolution, and deep-seated granulite xenoliths can offer direct information on the lower crust. Here, we report mineral chemistry, whole-rock major and trace elements, Sr-Nd isotopes and zircon U-Pb-Hf results for a suite of deep-seated crustal xenoliths, recently discovered in the Cenozoic basalts of the Nangaoya area in the northern part of the North China Craton (NCC). Based on the P-T estimates, these xenoliths including mafic, intermediate and felsic granulites and hornblendites were sampled from different levels of the lower crust. While a hornblendite has a flat REE pattern, all other xenoliths display LREE enrichment and depletion of Nb, Ta, Th and Ti. The mafic granulite xenolith has relatively high whole-rock εNd(t) value of - 13.37, and yields Mesozoic (188-59 Ma) zircons ages with high εHf(t) values from - 15.3 to - 9.2. The garnet-bearing intermediate granulite-facies rocks show low εNd(t) values from - 16.92 to - 17.48, and reveal both Paleoproterozoic (1948 Ma) and Mesozoic (222-63 Ma) zircon U-Pb ages. Their Mesozoic zircons have lower εHf(t) values (from - 18.4 to - 13.8) than those from the mafic xenolith. The remaining intermediate to felsic xenoliths show Paleoproterozoic zircon ages, and the lowest εNd(t) values (from - 20.78 to - 24.03). The mafic-intermediate granulites with Mesozoic zircons originated from the interaction of lower crust-derived magmas with mantle melts, with higher proportions of mantle magmas involved in the generation of mafic granulite, whereas intermediate to felsic xenoliths without Mesozoic zircons represent ancient Paleoproterozoic to Neoarchean deep crust. These deep-seated xenoliths reveal complicated crustal evolution processes, including crustal growth during Neoarchean (2.5-2.7 Ga), middle Paleoproterozoic (2.2-2.1 Ga) and Mesozoic, and reworking during early Paleoproterozoic, late

Geochemistry of abyssal peridotites from the super slow-spreading ...

Indian Academy of Sciences (India)

Serpentinites exhibit talc veins and major serpentine derived from ...... All trace element data used for this study are listed in table 5 ..... China for Distinguished Young Scholars (Grant. No. .... abyssal peridotites: A new perspective; Earth Planet.

Dynamics of Melting and Melt Migration as Inferred from Incompatible Trace Element Abundance in Abyssal Peridotites

Science.gov (United States)

Peng, Q.; Liang, Y.

2008-12-01

history. The abyssal peridotites used in this study are from Central Indian Ridge [1] and Vema Fracture Zone along the Mid-Atlantic Ridge [2]. As one of the end-member cases, we chose DMM as our starting mantle composition and assumed melting initiates in the spinel lherzolite field. To invert for F and R from a given set of trace element data, we considered a range of Fd values (0-5%). Overall, the degree of melting inferred from these two sets of data is not sensitive to the value of Fd used in our inversion and ranges from 9% to 25%. The relative rate of melt suction, R, however, depends slightly on the choice of Fd and ranges from 0.67 to 0.99 for Fd = 5% and 0.55 to 0.97 for Fd = 0. Hence there is a strong component of fractional melting beneath the mid-ocean ridge with an average of 80% melt being extracted through dunite channels. Further, our estimated R is inversely correlated with F, a robust feature independent of the choice of Fd. The upward decrease of R in the upwelling mantle column can be understood in terms of an upward increase in the volume fraction of high permeability dunite channels in the double-lithology region. And finally, given F and R, we found that the relative mass flux of the melt percolating in the lherzolite/harzburgite matrix also increases as a function of F (or height) in the melting column. This is a natural consequence of concurrent melting and melt migration in an upwelling steady-state mantle column. [1] Hellebrand et al. (2002) J. Petrol. 43, 2305-2338; [2] Brunelli et al. (2006) J. Petrol. 47, 745-771.

Direct evidence of hydration into mantle during shearing below a trasform fault: Prince Edward transform fault, Southwest Indian Ridge

Science.gov (United States)

Michibayashi, K.; Kakihata, Y.; Dick, H. J.

2017-12-01

Southwest Indian Ridge (SWIR) is located to the southwest of Rodriguez Triple Junction, where three Indian ocean ridges meet (Zhou & Dick, 2013, Nature). SWIR is one of the slowest spreading ocean ridges in the world. In this study, we studied microstructural development of 21 peridotite samples obtained from Prince Edward transform fault of SWIR by PROTEA5 cruise in 1983. The peridotites consist dominantly of olivine, orthopyroxene and clinopyroxene with minor amounts of amphibole and plagioclase as well as secondary minerals such as serpentine and magnetite. The peridotites were classified into four groups based on their microstructures: 3 ultramylonites mostly consisting of extremely fine crystals (3-5µm), 13 heterogeneous tectonites consisting of coarse-grained crystals and fine-grained matrix, 1 cataclasite and 4 intensely serpentinized peridotites. Olivine Mg# is 0.90-0.91 and spinel Cr# is 0.1-0.35. Amphibole crystals have chemical compositions of tremolite and magnesio-hornblende and they were intensely deformed within the ultramylonites and the heterogeneous tectonites, indicating that they have occurred before or during intense shearing in mantle. Moreover, extremely fine grain sizes of olivine and microboudin textures in both pyroxene and spinel crystals suggest that these peridotites have been sheared under high stress conditions. Furthermore, olivine crystal-fabrics within the amphibole bearing peridotites have B and E types that could be developed under hydrous conditions, whereas olivine fabrics within the other peridotites have A and D types that could be developed under anhydrous conditions (Karato et al., 2008, Annu. Rev. Earth Planet. Sci.). Consequently, the petrophysical characteristics of peridotites in this study indicate that the uppermost mantle below the Prince Edward transform fault has been locally but intensely hydrated during shearing due to transform movement.

Late Palaeozoic to Triassic formations unconformably deposited over the Ronda peridotites (Betic Cordilleras): Evidence for their Variscan time of crustal emplacement

Energy Technology Data Exchange (ETDEWEB)

Sanz de Galdeano, C.; Ruiz Cruz, M.D.

2016-07-01

The age of the emplacement of the Ronda Peridotites has been widely debated during recent decades, and ages ranging from the Palaeozoic to the early Miocene have been proposed, although most of the current interpretations suggest an Oligocene-Miocene age. In this article, we describe two meta-sedimentary formations (the lower one formed by detrital sediments and the upper one by marbles) that were unconformably deposited over the Ronda peridotites and now record low-grade metamorphism. The detrital formation contains layers of acidic rocks with an age of 269±9 Ma and the overlying marbles are assumed to be Triassic. The existence of these unconformable formations over the peridotites is crucial for the dating of the exhumation of the latter. The presence of peridotite clasts in the detrital formation indicates that peridotites were exposed during the Permian and other data suggest that peridotites were exhumed during the late Carboniferous. During the Alpine cycle, the peridotites operated as an element situated at the bottom of the tectonically higher Alpujarride/Sebtide unit (the Jubrique unit) and forming part of it, then being incorporated to the Alpine thrusts of this unit. (Author)

Petrogenesis of Neogene basaltic volcanism associated with the Lut block, eastern Iran: Implication for tectonic and metallogenic evolution

Science.gov (United States)

Saadat, Saeed

This dissertation presents petrochemical data concerning Neogene olivine basalts erupted both along the margins and within the micro-continental Lut block, eastern Iran, which is a part of the active Alpine-Himalayan orogenic belt. These data demonstrate the following: (1) Basalts that erupted from small monogenetic parasitic cones around the Bazman stratovolcano, Makran arc area, in the southern Lut block, are low-Ti sub-alkaline olivine basalts. Enrichments of LILE relative to LREE, and depletions in Nb and Ta relatively to LILE, are similar to those observed for other convergent plate boundary arc magmas around the world and suggest that these basalts formed by melting of subcontinental mantle modified by dehydration of the subducted Oman Sea oceanic lithosphere. (2) Northeast of Iran, an isolated outcrop of Neogene/Quaternary alkali olivine basalt, containing mantle and crustal xenoliths, formed by mixing of small melt fractions from both garnet and spinel-facies mantle. These melts rose to the surface along localized pathways associated with extension at the junction between the N-S right-lateral strike-slip faults and E-W left-lateral strike slip faults. The spinel-peridotite mantle xenoliths contained in the basalts, which equilibrated in the subcontinental lithosphere at depths of 30 to 60 km and temperatures of 965°C to 1065°C, do not preserve evidence of extensive metasomatic enrichment as has been inferred for the mantle below the Damavand volcano further to the west in north-central Iran. (3) Neogene mafic rocks within the central Lut block represent the last manifestation of a much more extensive mid-Tertiary magmatic event. These basalts formed from both OIB-like asthenosphere and subcontinental lithosphere which preserved chemical characteristics inherited from mid-Tertiary subduction associated with the collision of the Arabian with the Eurasian plate and closing of the Neotethys Ocean. Neogene/Quternary alkali olivine basalts erupted mainly along

Cation distribution in spinels and its effect on activity pick-up and passivation behaviour

International Nuclear Information System (INIS)

Subramanian, H.; Velmurugan, S.; Narasimhan, S.V.

2000-01-01

Spinels are found to be the major corrosion products in the primary heat transport system or nuclear reactors. These corrosion products are activated in the core and are picked up on the deposited corrosion product oxides, which lead to the radiation field buildup on out of core surfaces. In order to mitigate this phenomenon, it is extremely important to understand the structural changes that take place in a spinel in the primary heat transport system. Most of the spinels found in reactor systems are mixed spinels. Cation distribution in tetrahedral and octahedral sites of these spinels, which is temperature dependent, will affect the pickup of active metal ions from solution into these spinels. Distribution of cations in simple spinels was estimated by minimising the Gibbs energy change for the migration of ions between tetrahedral and octahedral sites, based on the assumption that it is the configurational entropy change for the process that dominates the distribution. Cation distribution for mixed spinels was also calculated using the same method. Energy demand for the exchange of an aqueous ion with these spinels has been estimated. (author)

Serpentinization: Getting water into a low permeability peridotite

Science.gov (United States)

Ulven, Ole Ivar

2017-04-01

Fluid consuming rock transformation processes occur in a variety of settings in the Earth's crust. One such process is serpentinization, which involves hydration of ultramafic rock to form serpentine. With peridotite being one of the dominating rocks in the oceanic crust, this process changes physical and chemical properties of the crust at a large scale, increases the amount of water that enters subduction zones, and might even affect plate tectonics te{jamtveit}. A significant number of papers have studied serpentinization in different settings, from reaction fronts progressing over hundreds of meters te{rudge} to the interface scale fracture initiation te{pluemper}. However, the process represents a complicated multi-physics problem which couples external stress, mechanical deformation, volume change, fracture formation, fluid transport, the chemical reaction, heat production and heat flow. Even though it has been argued that fracture formation caused by the volume expansion allows fluid infiltration into the peridotite te{rudge}, it remains unclear how sufficient water can enter the initially low permeability peridotite to pervasively serpentinize the rock at kilometre scale. In this work, we study serpentinization numerically utilizing a thermo-hydro-mechanical model extended with a fluid consuming chemical reaction that increases the rock volume, reduces its density and strength, changes the permeability of the rock, and potentially induces fracture formation. The two-way coupled hydromechanical model is based on a discrete element model (DEM) previously used to study a volume expanding process te{ulven_1,ulven_2} combined with a fluid transport model based on poroelasticity te{ulven_sun}, which is here extended to include fluid unsaturated conditions. Finally, a new model for reactive heat production and heat flow is introduced, to make this probably the first ever fully coupled chemo-thermo-hydromechanical model describing serpentinization. With this model

Electrochemically synthesized nanocrystalline spinel thin film for high performance supercapacitor

Energy Technology Data Exchange (ETDEWEB)

Gupta, Vinay [Carbon Technology Unit, Engineering Materials Division, National Physical Laboratory, New-Delhi, 110012 (India); Art, Science and Technology Center for Cooperative Research, Kyushu University, Kasuga-shi, Fukuoka, 816-8580 (Japan); Japan Science and Technology Agency, Kawaguchi-shi, Saitama, 332-0012 (Japan); Gupta, Shubhra; Miura, Norio [Art, Science and Technology Center for Cooperative Research, Kyushu University, Kasuga-shi, Fukuoka, 816-8580 (Japan)

2010-06-01

Spinels are not known for their supercapacitive nature. Here, we have explored electrochemically synthesized nanostructured NiCo{sub 2}O{sub 4} spinel thin-film electrode for electrochemical supercapacitors. The nanostructured NiCo{sub 2}O{sub 4} spinel thin film exhibited a high specific capacitance value of 580 F g{sup -1} and an energy density of 32 Wh kg{sup -1} at the power density of 4 kW kg{sup -1}, accompanying with good cyclic stability. (author)

Depleted and metasomatized oceanic lithosphere beneath La Palma, Canary Islands

Science.gov (United States)

Janisch, Astrid; Ntaflos, Theodoros

2017-04-01

Due to the inaccessibility of Earth's interior, xenoliths became the best possibility to study the chemical composition of the earth mantle as well as its various processes. Three samples out of the sample suite of mantle peridotites from San Antonio Volcano on La Palma, Canary Islands, have been chosen to illustrate three examples of diverse mantle metasomatic events. The first sample, a pyroxene-hornblende-peridotite, was influenced by an alkali-rich, silicic-hydrous undersaturated melt and/or fluid forming a conspicuous cross-cutting amphibole-apatite-dyke with several veins percolating through the rock. Forsterite content in olivine varies between 82.5 - 85.5 and 86.0 - 89.0, suggesting at least two different occurrences of metasomatic overprint. Clinopyroxenes are mostly found in association with amphibole and in textural equilibrium hinting that both minerals may have grown together, while orthopyroxene have only been found as remnant inclusions in olivine. These clinopyroxenes are Cr-Diopsides with En43.40-50.97-Wo43.99-48.64-Fs4.30-8.22 and Mg# between 85.54 and 92.36. Secondary clinopyroxenes are Ti-Augites with En39.86-46.81-Wo46.65-51.98-Fs5.86-8.72 and Mg# of 82.44 - 89.09. The second sample, a sp-dunite, is characterized by haüyne-bearing melt veins which clearly indicate host-basalt infiltration. The haüyne is always in contact with amphibole, spinel and clinopyroxene denoting that they have been formed at the same time because there is no evidence for reaction among these phases. The melt infiltration apparently took place prior to xenolith entrainment in the host basalt. Primary olivine has Fo content of 89.57 - 89.67 with NiO ranging from 0.32 - 0.334, in contrast Fo content in secondary olivine varies from 89.05 - 90.86 and NiO fluctuates between 0.24 - 0.31. Cr-Diopside compositions are in range of En41.63-47.05-Wo47.83-51-90-Fs4.93-6.64 and Mg# between 86.48 - 90.50. The third sample is also a sp-dunite and marked by a network of phlogopite

A Missing Link in Understanding Mantle Wedge Melting, Higashi-akaishi Peridotite, Japan

Science.gov (United States)

Till, C. B.; Carlson, R. W.; Grove, T. L.; Wallis, S.; Mizukami, T.

2009-12-01

The Sanbagawa subduction-type metamorphic belt in SW Japan represents the deepest exposed portion of a Mesozoic accretionary complex along the Japanese island arc. Located on the island of Shikoku, the Higashi-akaishi peridotite body is the largest ultramafic lens within the Sanbagawa belt and is dominantly composed of dunite, lherzolite and garnet clinopyroxenite, interfingered in one locality with quartz-rich eclogite. Previous work indicates the P-T history of the peridotite includes rapid prograde metamorphism with peak temperatures of 700-810°C and pressures of 2.9-3.8 GPa at approximately 110-120 Ma. Here we present major and trace element and isotopic data for samples within the Higashi-akaishi peridotite body that suggest it records subduction zone melting processes. Ultramafic samples range from 40-52 wt. % SiO2 and 21-45 wt. % MgO with olivine and clinopyroxene Mg#s as high as 0.93 and have trace element concentrations diagnostic of subduction zone processes. The quartz-rich eclogite contains 62 wt. % SiO2, 6 wt. % MgO and 13 wt. % Al2O3 and has trace element concentrations that are enriched relative to the ultramafic samples. 87Sr/86Sr (.703237-.704288), 143Nd/144Nd (ɛNd=+2-6) and Pb isotopic compositions are within the range of Japanese arc rocks. 187Os/188Os values range from typical mantle values (0.123-0.129), to slightly elevated (0.133) in one peridotite with an unusually low Os content, to a high of 0.145 in the quartz-rich eclogite. The presence of garnet porphyroblasts that enclose primary euhedral chlorite, together with the chemical evidence, suggest these samples are associated with mantle melting in the presence of H2O near their peak P-T conditions and may represent both residues and trapped melts within a paleo-mantle wedge. The peak P-T conditions of these rocks are also similar to the solidus conditions of H2O-saturated fertile mantle based on experimental determinations. Thus the Higashi-akaishi peridotite may be a real world analog

Application of nuclear analytical techniques to trace elements in cenozoic basalt and their mantle xenoliths from Aershan area in Inner Mongolia, China

International Nuclear Information System (INIS)

Yu Fusheng; Han Song; Huang Yuying; He Wei; Cao Jie; Wang Hongyue

2005-01-01

Basaltic samples from different locations in Aershan area determined by instrumental neutron activation analysis (INAA) have the same distribution patterns of REE and trace elements. The similar REE contents of the same minerals without inclusions from different xenolith suggest that the mantle source region under different active volcanoes have the same composition. The REE content differences between the same minerals with and without melt inclusions selected from the same mantle xenolith indicate that the melt inclusions are rich in REE. The same patterns of trace elements of inclusions and host minerals from different xenolith analyzed by SRXRF suggest that the mantle fluid has no notable heterogeneity in Aershan area. (authors)

Emplacement of Xenolith Nodules in the Kaupulehu Lava Flow, Hualalai Volcano, Hawaii

Science.gov (United States)

Guest, J. E.; Spudis, P. D.; Greeley, R.; Taylor, G. J.; Baloga, S. M.

1995-01-01

The basaltic Kaupulehu 1800-1801 lava flow of Hualalai Volcano, Hawaii contains abundant ultramafic xenoliths. Many of these xenoliths occur as bedded layers of semi-rounded nodules, each thinly coated with a veneer (typically 1 mm thick) of lava. The nodule beds are analogous to cobble deposits of fluvial sedimentary systems. Although several mechanisms have been proposed for the formation of the nodule beds, it was found that, at more than one locality, the nodule beds are overbank levee deposits. The geological occurrence of the nodules, certain diagnostic aspects of the flow morphology and consideration of the inferred emplacement process indicate that the Kaupulehu flow had an exceptionally low viscosity on eruption and that the flow of the lava stream was extremely rapid, with flow velocities of at least 10 m/s (more than 40 km/h. This flow is the youngest on Hualalai Volcano and future eruptions of a similar type would pose considerable hazard to life as well as property.

Preparation of the electrochemically formed spinel-lithium manganese oxides

Energy Technology Data Exchange (ETDEWEB)

Katakura, Katsumi; Wada, Kohei; Kajiki, Yoshiyuki; Yamamoto, Akiko [Department of Chemical Engineering, Nara National College of Technology, 22 Yata-cho Yamotokoriyama, Nara 639-1080 (Japan); Ogumi, Zempachi [Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8510 (Japan)

2009-04-01

Electrochemically formed spinel-lithium manganese oxides were synthesized from manganese hydroxides prepared by a cathodic electrochemical precipitation from various concentrations of manganese nitrate solutions. Two types of manganese hydroxides were formed from diluted and concentrated Mn(NO{sub 3}){sub 2} aqueous solutions. Uniform and equi-sized disk shaped Mn(OH){sub 2} crystals of 0.2-5 {mu}m in diameter were obtained on a Pt substrate after the electrochemical precipitation from lower concentration of ranging from 2 mmol dm{sup -3} to 2 mol dm{sup -3} Mn(NO{sub 3}){sub 2} aq., while the grass blade-like precipitate which is ascribed to manganese hydroxide with 20-80 {mu}m long and 1-5 {mu}m wide were formed from concentrated Mn(NO{sub 3}){sub 2} aq. Both manganese hydroxides gave the electrochemically formed spinel-LiMn{sub 2}O{sub 4} onto a Pt sheet, which is ready for electrochemical measurement, after calcination of the Li incorporated precipitate at 750 C without any additives. While the shape and size of the secondary particle frameworks (aggregates) of the electrochemically formed spinel-LiMn{sub 2}O{sub 4} can be controlled by the electrolysis conditions, the nanostructured primary crystals of 200 nm in diameter were obtained in all cases except that the fiber-like nanostructured spinel-LiMn{sub 2}O{sub 4} crystals with 200 nm in diameter were obtained from concentrated Mn(NO{sub 3}){sub 2} aq. Though these two types of electrochemically formed spinel-LiMn{sub 2}O{sub 4} showed well-shaped CVs even in higher scan rates, it would be suitable for high power density battery applications. These behaviors are assumed to be ascribed to the crystal size and shape of the processed spinel-LiMn{sub 2}O{sub 4}. (author)

PYROXENITE VEINS WITHIN SSZ PERIDOTITES – EVIDENCE OF MELT-ROCK INTERACTION (EGIINGOL MASSIF), MAJOR AND TRACE ELEMENT COMPOSITION OF MINERALS

OpenAIRE

A. A. Karimov; M A. Gornova; V. A. Belyaev

2017-01-01

Evidence of melt-rock reaction between suprasubduction zone (SSZ) peridotites and island arc boninititc and tholeiitic melts are identified. This process is the cause of replacive dunites and pyroxenite veins forming, which are represent the ways of island-arc melts migration. The peridotite-melt interaction is confirmed by compositional features of rocks and minerals. Influence of boninitic melt in peridotites of South Sandwich island arc leads to increasing of TiO2 and Cr-number (Cr#) in sp...

Thermal expansion of spinel-type Si3N4

DEFF Research Database (Denmark)

Paszkowics, W.; Minkikayev, R.; Piszora, P.

2004-01-01

The lattice parameter and thermal expansion coefficient (TEC) for the spinel-type Si3N4 phase prepared under high-pressure and high-temperature conditions are determined for 14 K......The lattice parameter and thermal expansion coefficient (TEC) for the spinel-type Si3N4 phase prepared under high-pressure and high-temperature conditions are determined for 14 K...

Nickel stabilization efficiency of aluminate and ferrite spinels and their leaching behavior.

Science.gov (United States)

Shih, Kaimin; White, Tim; Leckie, James O

2006-09-01

Stabilization efficiencies of spinel-based construction ceramics incorporating simulated nickel-laden waste sludge were evaluated and the leaching behavior of products investigated. To simulate the process of immobilization, nickel oxide was mixed alternatively with gamma-alumina, kaolinite, and hematite. These tailoring precursors are commonly used to prepare construction ceramics in the building industry. After sintering from 600 to 1480 degrees C at 3 h, the nickel aluminate spinel (NiAl204) and the nickel ferrite spinel (NiFe204) crystallized with the ferrite spinel formation commencing about 200-300 degrees C lower than for the aluminate spinel. All the precursors showed high nickel incorporation efficiencies when sintered at temperatures greater than 1250 degrees C. Prolonged leach tests (up to 26 days) of product phases were carried out using a pH 2.9 acetic acid solution, and the spinel products were invariably superior to nickel oxide for immobilization over longer leaching periods. The leaching behavior of NiAl2O4 was consistent with congruent dissolution without significant reprecipitation, but for NiFe2O4, ferric hydroxide precipitation was evident. The major leaching reaction of sintered kaolinite-based products was the dissolution of cristobalite rather than NiAl2O4. This study demonstrated the feasibility of transforming nickel-laden sludge into spinel phases with the use of readily available and inexpensive ceramic raw materials, and the successful reduction of metal mobility under acidic environments.

Moessbauer study of iron-cobalt-rhodium spinels

Energy Technology Data Exchange (ETDEWEB)

Spencer, C D; Smith, P A; Karnes, C M; Shepard, W A [Ithaca Coll., NY (USA). Dept. of Physics

1980-01-01

Moessbauer source and absorber studies have been carried out on the spinel system CoFesub(x)Rhsub(2-x)O/sub 4/ for x 0.005, 0.3, 0.5, 1.0, 1.2 and 1.5. For 0.005 =< x =< 1.2, the cation distribution is normal with Co/sup 2 +/ on A sites. At x = 1.5, the distribution is nearly inverse. In the cases x = 0.005 and 0.3, iron on the B sites does not produce a quadrupole doublet indicating that the B sites are cubic which is contrary to the usual case in spinels.

Reactive-brittle dynamics in peridotite alteration

Science.gov (United States)

Evans, O.; Spiegelman, M. W.; Kelemen, P. B.

2017-12-01

The interactions between reactive fluids and brittle solids are critical in Earth dynamics. Implications of such processes are wide-ranging: from earthquake physics to geologic carbon sequestration and the cycling of fluids and volatiles through subduction zones. Peridotite alteration is a common feature in many of these processes, which - despite its obvious importance - is relatively poorly understood from a geodynamical perspective. In particular, alteration reactions are thought to be self-limiting in nature, contradicting observations of rocks that have undergone 100% hydration/carbonation. One potential explanation of this observation is the mechanism of "reaction-driven cracking": that volume changes associated with these reactions are large enough to fracture the surrounding rock, leading to a positive feedback where new reactive surfaces are exposed and fluid pathways are created. The purpose of this study is to investigate the relative roles of reaction, elastic stresses and surface tension in alteration reactions. In this regard we derive a system of equations describing reactive fluid flow in an elastically deformable porous media, and explore them via a combination of analytic and numerical solutions. Using this model we show that the final stress state of a dry peridotite that has undergone reaction depends strongly on the rates of reaction versus fluid transport: significant fluid flow driven by pressure and/or surface tension gradients implies higher fractions of serpentinization, leaving behind a highly stressed residuum of partially reacted material. Using a model set-up that mimics a cylindrical triaxial apparatus we predict that the resulting stresses would lead to tensile failure and the generation of radially oriented cracks.

Cotectic proportions of olivine and spinel in olivine-tholeiitic basalt and evaluation of pre-eruptive processes

Science.gov (United States)

Roeder, Peter; Gofton, Emma; Thornber, Carl

2006-01-01

The volume %, distribution, texture and composition of coexisting olivine, Cr-spinel and glass has been determined in quenched lava samples from Hawaii, Iceland and mid-oceanic ridges. The volume ratio of olivine to spinel varies from 60 to 2800 and samples with >0·02% spinel have a volume ratio of olivine to spinel of approximately 100. A plot of wt % MgO vs ppm Cr for natural and experimental basaltic glasses suggests that the general trend of the glasses can be explained by the crystallization of a cotectic ratio of olivine to spinel of about 100. One group of samples has an olivine to spinel ratio of approximately 100, with skeletal olivine phenocrysts and small (within olivine phenocrysts is thought to be due to skeletal olivine phenocrysts coming into physical contact with spinel by synneusis during the chaotic conditions of ascent and extrusion. A second group of samples tend to have large olivine phenocrysts relatively free of included spinel, a few large (>100 μm) spinel crystals that show evidence of two stages of growth, and a volume ratio of olivine to spinel of 100 to well over 1000. The olivine and spinel in this group have crystallized more slowly with little physical interaction, and show evidence that they have accumulated in a magma chamber.

Detection of Mg spinel lithologies on central peak of crater ...

Indian Academy of Sciences (India)

identified Fe bearing Mg-spinel-rich rock types are defined by their strong 2-μm ... The Modified Gaussian Modeling (MGM) analysis ... study the deep crustal and/or upper mantle composition and may lead to a fresh ... Lunar surface; Mg-spinel; central peak; Theophilus; remote sensing. .... The explanation of these spec-.

Transparent magnesium aluminate spinel: a prospective biomaterial for esthetic orthodontic brackets.

Science.gov (United States)

Krishnan, Manu; Tiwari, Brijesh; Seema, Saraswathy; Kalra, Namitha; Biswas, Papiya; Rajeswari, Kotikalapudi; Suresh, Madireddy Buchi; Johnson, Roy; Gokhale, Nitin M; Iyer, Satish R; Londhe, Sanjay; Arora, Vimal; Tripathi, Rajendra P

2014-11-01

Adult orthodontics is recently gaining popularity due to its importance in esthetics, oral and general health. However, none of the currently available alumina or zirconia based ceramic orthodontic brackets meet the esthetic demands of adult patients. Inherent hexagonal lattice structure and associated birefringence limits the visible light transmission in polycrystalline alumina and make them appear white and non transparent. Hence focus of the present study was to assess the feasibility of using magnesium aluminate (MgAl2O4) spinel; a member of the transparent ceramic family for esthetic orthodontic brackets. Transparent spinel specimens were developed from commercially available white spinel powder through colloidal shaping followed by pressureless sintering and hot isostatic pressing at optimum conditions of temperature and pressure. Samples were characterized for chemical composition, phases, density, hardness, flexural strength, fracture toughness and optical transmission. Biocompatibility was evaluated with in-vitro cell line experiments for cytotoxicity, apoptosis and genotoxicity. Results showed that transparent spinel samples had requisite physico-chemical, mechanical, optical and excellent biocompatibility for fabricating orthodontic brackets. Transparent spinel developed through this method demonstrated its possibility as a prospective biomaterial for developing esthetic orthodontic brackets.

Structural investigation of the spinel phase formed in fuel CRUD before and after zinc injection

International Nuclear Information System (INIS)

Chen, J.

2002-01-01

Spinel phase is an important constituent of fuel CRUD. Since it can accommodate 60 Co in its crystal structure, its stability in reactor water environment is crucial for the radioactivity control in LWR plants. With increasing curiosity about zinc injection technology, the mechanism of the interaction of zinc with the spinel has drawn much attention. This paper describes the crystal and microstructures of spinel phase in the fuel CRUD collected on four fuel rods of 1- and 5-cycle, respectively, from Barsebaeck 2 BWR before and after zinc injection operation. High precision X-ray powder diffraction technique has been applied to identify the phase compositions of fuel CRUD and to measure the cell length of the spinel phase formed. The results show that, after about 1-cycle zinc injection operation, the tenacious CRUD formed on the fresh fuel rod contains defective zinc oxide, in addition to hematite and spinel as commonly seen. Moreover, the phase ratio of spinel to hematite is much increased. The cell length of the spinel is increased accordingly, which is the direct evidence for the presence of zinc in the spinel structure. For the 5-cycle rod, however, neither zinc oxide nor any change in the phase ratio has been detected. The cell length of the spinel has been increased, in a less degree, however, as compared to that for the 1-cycle rod. The cell lengths of spinel are similar in both tenacious and loose CRUD layers, indicating that zinc was able to easily penetrate through the tenacious CRUD layer. (authors)

Detoxification and immobilization of chromite ore processing residue in spinel-based glass-ceramic

Energy Technology Data Exchange (ETDEWEB)

Liao, Chang-Zhong [Guangdong Key Laboratory of Agricultural Environment Pollution Integrated Control, Guangdong Institute of Eco-Environmental and Soil Sciences, Guangzhou 510650 (China); Department of Civil Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong Special Administrative Region (China); Tang, Yuanyuan [School of Environmental Science and Engineering, South University of Science and Technology of China, Shenzhen 518055 (China); Lee, Po-Heng [Department of Civil & Environmental Engineering, The Hong Kong Polytechnic University, Hong Kong Special Administrative Region (China); Liu, Chengshuai, E-mail: csliu@soil.gd.cn [Guangdong Key Laboratory of Agricultural Environment Pollution Integrated Control, Guangdong Institute of Eco-Environmental and Soil Sciences, Guangzhou 510650 (China); State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang 550009 (China); Shih, Kaimin, E-mail: kshih@hku.hk [Department of Civil Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong Special Administrative Region (China); Li, Fangbai [Guangdong Key Laboratory of Agricultural Environment Pollution Integrated Control, Guangdong Institute of Eco-Environmental and Soil Sciences, Guangzhou 510650 (China)

2017-01-05

Graphical abstract: Schematic illustration of detoxification and immobilization of chromite ore processing residue in spinel-based glass-ceramic matrix. All Cr(VI) species is reduced to Cr(III) and most chromium contents are incorporated into spinel structure where the residual chromium are resided in the glass networks. - Highlights: • COPR was detoxified and immobilized in a spinel-based glass-ceramic matrix. • Cr-rich crystalline phase was determined to be MgCr{sub 1.32}Fe{sub 0.19}Al{sub 0.49}O{sub 4} spinel. • The partitioning ratio of Cr into spinel in the glass-ceramic can be up to 77%. • No Cr(VI) was observed after conversion of COPR into a glass-ceramic. • TCLP results demonstrate the superiority of the final product in immobilizing Cr. - Abstract: A promising strategy for the detoxification and immobilization of chromite ore processing residue (COPR) in a spinel-based glass-ceramic matrix is reported in this study. In the search for a more chemically durable matrix for COPR, the most critical crystalline phase for Cr immobilization was found to be a spinel solid solution with a chemical composition of MgCr{sub 1.32}Fe{sub 0.19}Al{sub 0.49}O{sub 4}. Using Rietveld quantitative X-ray diffraction analysis, we identified this final product is with the phases of spinel (3.5 wt.%), diopside (5.2 wt.%), and some amorphous contents (91.2 wt.%). The partitioning ratio of Cr reveals that about 77% of the Cr was incorporated into the more chemically durable spinel phase. The results of Cr K-edge X-ray absorption near-edge spectroscopy show that no Cr(VI) was observed after conversion of COPR into a glass-ceramic, which indicates successful detoxification of Cr(VI) into Cr(III) in the COPR-incorporated glass-ceramic. The leaching performances of Cr{sub 2}O{sub 3} and COPR-incorporated glass-ceramic were compared with a prolonged acid-leaching test, and the results demonstrate the superiority of the COPR-incorporated glass-ceramic matrix in the

Detoxification and immobilization of chromite ore processing residue in spinel-based glass-ceramic

International Nuclear Information System (INIS)

Liao, Chang-Zhong; Tang, Yuanyuan; Lee, Po-Heng; Liu, Chengshuai; Shih, Kaimin; Li, Fangbai

2017-01-01

Graphical abstract: Schematic illustration of detoxification and immobilization of chromite ore processing residue in spinel-based glass-ceramic matrix. All Cr(VI) species is reduced to Cr(III) and most chromium contents are incorporated into spinel structure where the residual chromium are resided in the glass networks. - Highlights: • COPR was detoxified and immobilized in a spinel-based glass-ceramic matrix. • Cr-rich crystalline phase was determined to be MgCr 1.32 Fe 0.19 Al 0.49 O 4 spinel. • The partitioning ratio of Cr into spinel in the glass-ceramic can be up to 77%. • No Cr(VI) was observed after conversion of COPR into a glass-ceramic. • TCLP results demonstrate the superiority of the final product in immobilizing Cr. - Abstract: A promising strategy for the detoxification and immobilization of chromite ore processing residue (COPR) in a spinel-based glass-ceramic matrix is reported in this study. In the search for a more chemically durable matrix for COPR, the most critical crystalline phase for Cr immobilization was found to be a spinel solid solution with a chemical composition of MgCr 1.32 Fe 0.19 Al 0.49 O 4 . Using Rietveld quantitative X-ray diffraction analysis, we identified this final product is with the phases of spinel (3.5 wt.%), diopside (5.2 wt.%), and some amorphous contents (91.2 wt.%). The partitioning ratio of Cr reveals that about 77% of the Cr was incorporated into the more chemically durable spinel phase. The results of Cr K-edge X-ray absorption near-edge spectroscopy show that no Cr(VI) was observed after conversion of COPR into a glass-ceramic, which indicates successful detoxification of Cr(VI) into Cr(III) in the COPR-incorporated glass-ceramic. The leaching performances of Cr 2 O 3 and COPR-incorporated glass-ceramic were compared with a prolonged acid-leaching test, and the results demonstrate the superiority of the COPR-incorporated glass-ceramic matrix in the immobilization of Cr. The overall results suggest that

Composition of the earth's upper mantle. II - Volatile trace elements in ultramafic xenoliths

Science.gov (United States)

Morgan, J. W.; Wandless, G. A.; Petrie, R. K.; Irving, A. J.

1980-01-01

Radiochemical neutron activation analysis was used to determine the nine volatile elements Ag, Bi, Cd, In, Sb, Se, Te, Tl, and Zn in 19 ultramafic rocks, consisting mainly of spinel and garnet lherzolites. A sheared garnet lherzolite, PHN 1611, may approximate undepleted mantle material and tends to have a higher volatile element content than the depleted mantle material represented by spinel lherzolites. Comparisons of continental basalts with PHN 1611 and of oceanic ridge basalts with spinel lherzolites show similar basalt: source material partition factors for eight of the nine volatile elements, Sb being the exception. The strong depletion of Te and Se in the mantle, relative to lithophile elements of similar volatility, suggests that 97% of the earth's S, Se and Te may be in the outer core.

Serpentinization of abyssal peridotites from the MARK area, Mid-Atlantic Ridge: Sulfur geochemistry and reaction modeling

Science.gov (United States)

Alt, J.C.; Shanks, Wayne C.

2003-01-01

The opaque mineralogy and the contents and isotope compositions of sulfur in serpentinized peridotites from the MARK (Mid-Atlantic Ridge, Kane Fracture Zone) area were examined to understand the conditions of serpentinization and evaluate this process as a sink for seawater sulfur. The serpentinites contain a sulfur-rich secondary mineral assemblage and have high sulfur contents (up to 1 wt.%) and elevated ??34Ssulfide (3.7 to 12.7???). Geochemical reaction modeling indicates that seawater-peridotite interaction at 300 to 400??C alone cannot account for both the high sulfur contents and high ??34Ssulfide. These require a multistage reaction with leaching of sulfide from subjacent gabbro during higher temperature (???400??C) reactions with seawater and subsequent deposition of sulfide during serpentinization of peridotite at ???300??C. Serpentinization produces highly reducing conditions and significant amounts of H2 and results in the partial reduction of seawater carbonate to methane. The latter is documented by formation of carbonate veins enriched in 13C (up to 4.5???) at temperatures above 250??C. Although different processes produce variable sulfur isotope effects in other oceanic serpentinites, sulfur is consistently added to abyssal peridotites during serpentinization. Data for serpentinites drilled and dredged from oceanic crust and from ophiolites indicate that oceanic peridotites are a sink for up to 0.4 to 6.0 ?? 1012 g seawater S yr-1. This is comparable to sulfur exchange that occurs in hydrothermal systems in mafic oceanic crust at midocean ridges and on ridge flanks and amounts to 2 to 30% of the riverine sulfate source and sedimentary sulfide sink in the oceans. The high concentrations and modified isotope compositions of sulfur in serpentinites could be important for mantle metasomatism during subduction of crust generated at slow spreading rates. ?? 2003 Elsevier Science Ltd.

Short wavelength lateral variability of lithospheric mantle beneath the Middle Atlas (Morocco) as recorded by mantle xenoliths

Science.gov (United States)

El Messbahi, Hicham; Bodinier, Jean-Louis; Vauchez, Alain; Dautria, Jean-Marie; Ouali, Houssa; Garrido, Carlos J.

2015-05-01

The Middle Atlas is a region where xenolith-bearing volcanism roughly coincides with the maximum of lithospheric thinning beneath continental Morocco. It is therefore a key area to study the mechanisms of lithospheric thinning and constrain the component of mantle buoyancy that is required to explain the Moroccan topography. Samples from the two main xenolith localities, the Bou Ibalghatene and Tafraoute maars, have been investigated for their mineralogy, microstructures, crystallographic preferred orientation, and whole-rock and mineral compositions. While Bou Ibalghatene belongs to the main Middle Atlas volcanic field, in the 'tabular' Middle Atlas, Tafraoute is situated about 45 km away, on the North Middle Atlas Fault that separates the 'folded' Middle Atlas, to the South-East, from the 'tabular' Middle Atlas, to the North-West. Both xenolith suites record infiltration of sub-lithospheric melts that are akin to the Middle Atlas volcanism but were differentiated to variable degrees as a result of interactions with lithospheric mantle. However, while the Bou Ibalghatene mantle was densely traversed by high melt fractions, mostly focused in melt conduits, the Tafraoute suite records heterogeneous infiltration of smaller melt fractions that migrated diffusively, by intergranular porous flow. As a consequence the lithospheric mantle beneath Bou Ibalghaten was strongly modified by melt-rock interactions in the Cenozoic whereas the Tafraoute mantle preserves the record of extensional lithospheric thinning, most likely related to Mesozoic rifting. The two xenolith suites illustrate distinct mechanisms of lithospheric thinning: extensional thinning in Tafraoute, where hydrous incongruent melting triggered by decompression probably played a key role in favouring strain localisation, vs. thermal erosion in Bou Ibalghatene, favoured and guided by a dense network of melt conduits. Our results lend support to the suggestion that lithospheric thinning beneath the Atlas

Petrological and geochemical studies of mantle xenoliths from La Palma, Canary Islands

Science.gov (United States)

Janisch, Astrid; Ntaflos, Theodoros

2015-04-01

La Palma is the second youngest island, after El Hierro, of the Canary archipelago. The archipelago consists of seven large islands, forming an east-west-trending island chain, and several seamounts. All together they form a volcanic belt of around 800 km length and 450 km width, which presumably comprises roughly the Canary hotspot. The islands are located off the western coast of Morocco, Africa. The distance ranges from 100 km to 500 km. Concurrently with the distance, subaerial volcanism age progresses from the oldest lava in the east to the youngest in the west of the archipelago. Presently, La Palma is in the shield building stage of growth (alongside with El Hierro and Tenerife) and is furthermore the fastest growing island of the Canary archipelago. Historical volcanic eruptions are restricted on the younger islands, La Palma and El Hierro, with the last eruption at the south end of La Palma in 1971. Mantle xenoliths described in this work were collected at the slopes of San Antonio Volcano, Fuencaliente, brought to the surface during the 1677/1678 eruption. The mantle xenolith collection comprises sp-lherzolites, sp-harzburgites and pyroxenites. The texture can be distinguished between coarse-grained matrix and fine-grained veins in various thicknesses, mostly with olivine and pyroxene but also with amphibole, phlogopite as well as apatite. Mineral analyses reveal the existence of primary and secondary ol, cpx and opx. Primary ol has Fo contents of 89.2 to 91.7 and NiO ranging from 0.3 to 0.45 wt.%, whereas secondary ol show Fo values of 78.4 to 91.9 but with NiO below 0.3 wt.%. Primary cpx are predominantly Cr-Diopsides with En48.7-51.9-Wo43.5-44.3-Fs4.1-4.9 and Mg# of 91.5 to 92.4. Secondary cpx, primarily Ti-Augit, display En36.7-44.4-Wo47.7-49.6-Fs6.7-13.0 and Mg# of 75.3 to 90.8. Primary opx compositions are in range of En89.3-90.6-Wo1.3-1.5-Fs8.1-9.3 with Mg# between 90.7 and 92.0. Secondary opx exhibit En88.7-89.2-Wo1.7-1.9-Fs9.1-9.5 and Mg# of 90

Geochemistry and petrology of pyroxenite xenoliths from Cenozoic alkaline basalts, Bohemian Massif

Czech Academy of Sciences Publication Activity Database

Ackerman, Lukáš; Špaček, Petr; Medaris Jr., G.; Hegner, E.; Svojtka, Martin; Ulrych, Jaromír

2012-01-01

Roč. 57, č. 4 (2012), s. 199-219 ISSN 1802-6222 R&D Projects: GA ČR(CZ) GA205/09/1170 Institutional research plan: CEZ:AV0Z30130516; CEZ:AV0Z30120515 Institutional support: RVO:67985831 ; RVO:67985530 Keywords : pyroxenite * xenolith * Cenozoic * basalt * Sr-Nd isotopes * geothermobarometry Subject RIV: DD - Geochemistry Impact factor: 0.804, year: 2012

Cation disorder in high-dose, neutron-irradiated spinel

International Nuclear Information System (INIS)

Sickafus, K.E.; Larson, A.C.; Yu, N.; Nastasi, M.; Hollenberg, G.W.; Garner, F.A.; Bradt, R.C.

1994-08-01

The objective of this effort is to determine whether MgAl 2 O 4 spinel is a suitable ceramic for fusion applications. Here, the crystal structures of MgAl 2 O 4 spinel single crystals irradiated to high neutron fluences [>5·10 26 n/m 2 (E n > 0.1 MeV)] were examined by neutron diffraction. Crystal structure refinement of the highest dose sample indicated that the average scattering strength of the tetrahedral crystal sites decreased by ∼ 20% while increasing by ∼ 8% on octahedral sites. Since the neutron scattering length for Mg is considerably larger than for Al, this results is consistent with site exchange between Mg 2+ ions on tetrahedral sites and Al 3+ ions on octahedral sites. Least-squares refinements also indicated that, in all irradiated samples, at least 35% of Mg 2+ and Al 3+ ions in the crystal experienced disordering replacements. This retained dpa on the cation sublattices is the largest retained damage ever measured in an irradiated spinel material

Peridotites and mafic igneous rocks at the foot of the Galicia Margin: an oceanic or continental lithosphere? A discussion

Energy Technology Data Exchange (ETDEWEB)

Korprobst, J.; Chazot, G.

2016-10-01

An ultramafic/mafic complex is exposed on the sea floor at the foot of the Galicia Margin (Spain and Portugal). It comprises various types of peridotites and pyroxenites, as well as amphibole-diorites, gabbros, dolerites and basalts. For chronological and structural reasons (gabbros were emplaced within peridotites before the continental break-up) this unit cannot be assigned to the Atlantic oceanic crust. The compilation of all available petrological and geochemical data suggests that peridotites are derived from the sub-continental lithospheric mantle, deeply transformed during Cretaceous rifting. Thus, websterite dykes extracted from the depleted MORB mantle reservoir (DMM), were emplaced early within the lithospheric harzburgites; subsequent boudinage and tectonic dispersion of these dykes in the peridotites, during deformation stages at the beginning of rifting, resulted in the formation of fertile but isotopically depleted lherzolites. Sterile but isotopically enriched websterites, would represent melting residues in the peridotites, after significant partial melting and melt extraction related to the thermal erosion of the lithosphere. The latter melts are probably the source of brown amphibole metasomatic crystallization in some peridotites, as well as of the emplacement of amphibole-diorite dykes. Melts directly extracted from the asthenosphere were emplaced as gabbro within the sub-continental mantle. Mixing these DMM melts together with the enriched melts extracted from the lithosphere, provided the intermediate isotopic melt-compositions - in between the DMM and Oceanic Islands Basalts reservoir - observed for the dolerites and basalts, none of which are characterized by a genuine N-MORB signature. An enriched lithospheric mantle, present prior to rifting of the Galicia margin, is in good agreement with data from the Messejana dyke (Portugal) and more generally, with those of all continental tholeiites of the Central Atlantic Magmatic Province (CAMP

Effect of lapping slurry on critical cutting depth of spinel

International Nuclear Information System (INIS)

Wang, Zhan-kui; Wang, Zhuan-kui; Zhu, Yong-wei; Su, Jian-xiu

2015-01-01

Highlights: • Measured spinel wafers’ hardness and crack length in different slurries. • Evaluated the softened layer thickness in different slurries. • Discussed the effect of slurries on critical cutting depth of spinel. - Abstract: The critical cutting depth for lapping process is very important because it influences the mode of material removal. In this paper, a serial of microscopic indentation experiments were carried out for measuring spinel wafers’ hardness and crack length in different lapping slurries. Their critical cutting depth and fracture toughness were calculated. X-ray photoelectron spectroscopy (XPS) was also employed to study the surface chemical composition and softened layer thickness of wafers in different slurries. Experimental results indicate that the softened layers of spinel wafers are formed due to the corrosion of lapping slurries, which leads to a lower hardness and a larger fracture toughness of samples, and increases the critical cutting depth. Among them, the critical cutting depth in ethylene glycol solution is the largest and up to 21.8 nm. The increase of critical cutting depth is helpful to modify the surface quality of the work-piece being lapped via ductile removal mode instead of brittle fracture mode

A comparison between the irradiation damage response of spinel and zirconia due to Xe ion bombardment

International Nuclear Information System (INIS)

Sickafus, K.E.; Wetteland, C.J.; Baker, N.P.; Yu Ning; Devanathan, R.; Nastasi, M.; Bordes, N.

1998-01-01

The mechanical properties of Xe-implanted spinel and cubic zirconia surfaces, as determined by nano-indentation measurements, are distinct and the differences can be related to their microstructures. Upon Xe 2+ ion irradiation to high dose at cryogenic temperature (120 K), the Young's modulus of irradiated spinel falls dramatically until the modulus is only about 3/4 the un-irradiated value. The maximum modulus occurs concurrent with the formation of a metastable crystalline phase of spinel. The subsequent elastic softening at higher Xe 2+ doses is an indication of the onset of amorphization of the spinel. Xe-implanted zirconia surfaces behave differently, in all cases showing almost no change in elastic modulus with increasing Xe 2+ ion dose. This is consistent with microstructural observations of Xe-implanted zirconia crystals which, unlike spinel, show no change in crystal structure with increasing ion dose. The hardness of both spinel and zirconia increases slightly for low Xe 2+ ion doses. At higher doses, zirconia shows little change in hardness, while the hardness of the implanted spinel falls by more than a factor of two. The initial increase in hardness of both spinel and zirconia is consistent with point defect accumulation and the precipitation of small interstitial clusters, while the drop in hardness of spinel at high Xe 2+ ion doses is due to the formation of an amorphous phase. (orig.)

Within-plate Cenozoic Volcanism and Mantle Sources Within The Western-central Mediterranean Area

Science.gov (United States)

Beccaluva, L.; Bianchini, G.; Bonadiman, C.; Coltorti, M.; Siena, F.

An integrated study of anorogenic basic magmas and entrained mantle xenoliths rep- resents a promising approach for a comprehension of the magmatogenic events occur- ring within the lithospheric mantle in the western-central Mediterranean area. In this contribution we review the geochemical characteristics of mafic lavas and associated peridotite xenoliths from three anorogenic volcanic districts: Pliocene-Quaternary vol- canism of Sardinia; Pliocene-Quaternary volcanism of the Iblean area (eastern Sicily); Paleocene-Oligocene Veneto Volcanic Province. Investigations have been focused on 1) petrological features of parental magmas, which may contribute to infer the com- positional characteristics of mantle sources and to constrain the modes of partial melt- ing; 2) modelling the depletion events and metasomatic enrichments in mantle xeno- liths of the three volcanic districts, as well as the nature of their causative agents. Petrological features and Sr-Nd-Pb isotopic data, both of lava and xenoliths, indicate that DM+HIMU components distinguish the lithospheric mantle sections of Iblean and Veneto Volcanic Provinces. On the other hand, lavas and xenoliths from Sardinia display a significant different isotopic signature characterised by DM+EM1. Similar geochemical fingerprints, i.e. the significant presence of EM components are gener- ally recorded by mafic lavas and mantle xenoliths from the European Plate, whereas they are not observed in the stable African lithospheric domain.

Method of microbially producing metal gallate spinel nano-objects, and compositions produced thereby

Science.gov (United States)

Duty, Chad E.; Jellison, Jr., Gerald E.; Love, Lonnie J.; Moon, Ji Won; Phelps, Tommy J.; Ivanov, Ilia N.; Kim, Jongsu; Park, Jehong; Lauf, Robert

2018-01-16

A method of forming a metal gallate spinel structure that includes mixing a divalent metal-containing salt and a gallium-containing salt in solution with fermentative or thermophilic bacteria. In the process, the bacteria nucleate metal gallate spinel nano-objects from the divalent metal-containing salt and the gallium-containing salt without requiring reduction of a metal in the solution. The metal gallate spinel structures, as well as light-emitting structures in which they are incorporated, are also described.

Geochemistry and petrogenesis of serpentinite from the Ingalls ophiolite complex, central Cascades, Washington

Science.gov (United States)

MacDonald, J. H., Jr.; Milliken, S. H.; Zalud, K. M.

2017-12-01

The Jurassic Ingalls ophiolite complex is located in the central Cascades, Washington State. This ophiolite predominantly consists of three variably serpentinized mantle units. Serpentinite occurs as massive replacing peridotite, or as highly sheared fault zones cutting other rocks. Mylonitic serpentinite forms a large-scale mélange in the middle of the ophiolite, and is interpreted as a fracture zone. Whole-rock and mineral geochemistry of the massive serpentinite was done to understand the metasomatic process and identify the possible protoliths of these rocks. Whole-rock major and trace elements of the massive serpentinite are similar to modern peridotites. The majority of samples analyzed are strongly serpentinized, while a few were moderately to weakly altered. Ca, Mg, and Al suggest these rocks formed from serpentinized harzburgite and dunite with minor lherzolite. All samples have positive Eu/Eu*. Serpentinites plot in fields defined by modern abyssal and forearc peridotites. Trace elements suggests the protoliths underwent variable amounts of mantel depletion (5-20%). Serpentine and relic igneous minerals were analyzed by EPMA at the Florida Center for Analytical Electron Microscopy. The serpentine dose not chemically display brucite mixing, has minor substitution of Fe, Ni, and Cr for Mg, and minor Al substitution for Si. Bastites have higher Ni than replaced olivine. Mineral chemistry, high LOI, and X-ray diffraction suggest lizardite is the primary serpentine polymorph, with minor chrysotile also occurring. Relic Al-chromite and Cr-spinel commonly have Cr-magnetite rims. These relic cores have little SiO2 and Fe3+, suggesting the spinels are well preserved. Most spinels plot in overlap fields defined by abyssal and arc peridotite, while two samples plot entirely in arc fields. Relic olivine have Fo90 to Fo92 and plot along the mantle array. Relic pyroxene are primarily enstatite, with lesser high-Ca varieties. Relic minerals plot near fields defined by

Dielectric and impedance study of praseodymium substituted Mg-based spinel ferrites

Energy Technology Data Exchange (ETDEWEB)

Farid, Hafiz Muhammad Tahir, E-mail: tahirfaridbzu@gmail.com [Department of Physics, Bahauddin Zakariya, University Multan, 60800 (Pakistan); Ahmad, Ishtiaq; Ali, Irshad [Department of Physics, Bahauddin Zakariya, University Multan, 60800 (Pakistan); Ramay, Shahid M. [College of Science, Physics and Astronomy Department, King Saud University, P.O. Box 2455, 11451 Riyadh (Saudi Arabia); Mahmood, Asif [Chemical Engineering Department, College of Engineering, King Saud University, Riyadh (Saudi Arabia); Murtaza, G. [Centre for Advanced Studies in Physics, GC University, Lahore 5400 (Pakistan)

2017-07-15

Highlights: • Magnesium based spinel ferrites were successfully synthesized by sol-gel method. • Dielectric constant shows the normal spinel ferrites behavior. • The dc conductivity are found to decrease with increasing temperature. • The samples with low conductivity have high values of activation energy. • The Impedance decreases with increasing frequency of applied field. - Abstract: Spinel ferrites with nominal composition MgPr{sub y}Fe{sub 2−y}O{sub 4} (y = 0.00, 0.025, 0.05, 0.075, 0.10) were prepared by sol-gel method. Temperature dependent DC electrical conductivity and drift mobility were found in good agreement with each other, reflecting semiconducting behavior. The dielectric properties of all the samples as a function of frequency (1 MHz–3 GHz) were measured at room temperature. The dielectric constant and complex dielectric constant of these samples decreased with the increase of praseodymium concentration. In the present spinel ferrite, Cole–Cole plots were used to separate the grain and grain boundary’s effects. The substitution of praseodymium ions in Mg-based spinel ferrites leads to a remarkable rise of grain boundary’s resistance as compared to the grain’s resistance. As both AC conductivity and Cole–Cole plots are the functions of concentration, they reveal the dominant contribution of grain boundaries in the conduction mechanism. AC activation energy was lower than dc activation energy. Temperature dependence normalized AC susceptibility of spinel ferrites reveals that MgFe{sub 2}O{sub 4} exhibits multi domain (MD) structure with high Curie temperature while on substitution of praseodymium, MD to SD transitions occurs. The low values of conductivity and low dielectric loss make these materials best candidate for high frequency application.

Gravimetric structure for the abyssal mantle massif of Saint Peter and Saint Paul peridotite ridge, Equatorial Atlantic Ocean, and its relation to active uplift

Directory of Open Access Journals (Sweden)

KENJI F. MOTOKI

2014-06-01

Full Text Available This paper presents gravimetric and morphologic analyses based on the satellite-derived data set of EGM2008 and TOPEX for the area of the oceanic mantle massif of the Saint Peter and Saint Paul peridotite ridge, Equatorial Atlantic Ocean. The free-air anomaly indicates that the present plate boundary is not situated along the longitudinal graben which cuts peridotite ridge, but about 20 km to the north of it. The high Bouguer anomaly of the peridotite ridge suggests that it is constituted mainly by unserpentinised ultramafic rocks. The absence of isostatic compensation and low-degree serpentinisation of the ultramafic rocks indicate that the peridotite ridge is sustained mainly by active tectonic uplift. The unparallel relation between the transform fault and the relative plate motion generates near north-south compression and the consequent tectonic uplift. In this sense, the peridotite massif is a pressure ridge due to the strike-slip displacement of the Saint Paul Transform Fault.

Enhancement photocatalytic activity of spinel oxide (Co, Ni3O4 by combination with carbon nanotubes

Directory of Open Access Journals (Sweden)

Kahdum Bashaer J.

2017-09-01

Full Text Available In this study, some types of composites consisting of multi-walled carbon nanotubes (MWCNTs and spinel oxide (Co, Ni3O4 were synthesized by simple evaporation method. These composites were characterized by UV–Vis diffuse reflectance spectroscopy, X-rays diffraction(XRD, Scanning electron microscopy (SEM and specific surface area(SBET. The photocatalytic activity of the prepared composites was investigated by the following removal of Bismarck brown G (BBG dye from its aqueous solutions. The obtained results showed that using MWCNTs in combination with spinel oxide to produced composites (spinel/MWCNTs which succeeded in increasing the activity of spinel oxide and exhibited higher photocatalytic activity than spinel oxide alone. Also it was found that, multiwalled carbon nanotubes were successful in increasing the adsorption and improving the activity of photocatalytic degradation of Bismarck brown G dye(BBG. The obtained results showed that spinel/MWCNTs was more active in dye removal in comparison with each of spinel oxide and MWCNTs alone under the same reaction conditions. Also band gap energies for the prepared composites showed lower values in comparison with neat spinel. This point represents a promising observation as these composites can be excited using a lower energy radiation sources.

The Lu-Hf isotope composition of cratonic lithosphere: disequilibrium between garnet and clinopyroxene in kimberlite xenoliths

NARCIS (Netherlands)

Simon, N.S.C.; Carlson, R.W.; Pearson, D.G.; Davies, G.R.

2002-01-01

12th Annual V.M. Goldschmidt Conference Davos Switzerland, The Lu-Hf isotope composition of cratonic lithosphere: disequilibrium between garnet and clinopyroxene in kimberlite xenoliths (DTM, Carnegie Institution of Washington), Pearson, D.G. (University of Durham)

Experimental Melting Study of Basalt-Peridotite Hybrid Source: Melting model of Hawaiian plume

Science.gov (United States)

Takahashi, E.; Gao, S.

2015-12-01

Eclogite component entrained in ascending plume is considered to be essentially important in producing flood basalts (e.g., Columbia River basalt, Takahashi et al., 1998 EPSL), alkalic OIBs (e.g., Kogiso et al.,2003), ferro-picrites (Tuff et al.,2005) and Hawaiian shield lavas (e.g., Hauri, 1996; Takahashi & Nakajima, 2002, Sobolev et al.,2005). Size of the entrained eclogite, which controls the reaction rates with ambient peridotite, however, is very difficult to constrain using geophysical observation. Among Hawaiian shield volcanoes, Koolau is the most enriched end-member in eclogite component (Frey et al, 1994). Reconstruction of Koolau volcano based on submarine study on Nuuanu landslide (AGU Monograph vol.128, 2002, Takahashi Garcia Lipman eds.) revealed that silica-rich tholeiite appeared only at the last stage (Makapuu stage) of Koolau volcano. Chemical compositions of lavas as well as isotopes change abruptly and coherently across a horizon (Shinozaki et al. and Tanaka et al. ibid.). Based on these observation, Takahashi & Nakajima (2002 ibid) proposed that the Makapuu stage lava in Koolau volcano was supplied from a single large eclogite block. In order to study melting process in Hawaiian plume, high-pressure melting experiments were carried out under dry and hydrous conditions with layered eclogite/peridotite starting materials. Detail of our experiments will be given by Gao et al (2015 AGU). Combined previous field observation with new set of experiments, we propose that variation in SiO2 among Hawaiian tholeiites represent varying degree of wall-rock interaction between eclogite and ambient peridotite. Makapuu stage lavas in Koolau volcano represents eclogite partial melts formed at ~3 GPa with various amount of xenocrystic olivines derived from Pacific plate. In other words, we propose that "primary magma" in the melting column of Hawaiian plume ranges from basaltic andesite to ferro-picrite depending on the lithology of the source. Solidus of

The Universal Cpx Jd-Di barometer for mantle peridotite eclogite and pyroxenites and it using for the mantle petrology

Science.gov (United States)

Ashchepkov, Igor

2015-04-01

The Jd-Di exchange in clinopyroxenes used for the calibration of pyroxene barometer (Ashchepkov, 2000;2002; Ashchepkov et al 2010;2011;2012) was transformed to make one universal equation for mantle peridotite eclogites and pyroxenites. The original barometer (Ashchepkov, 2002) calibrated on pressures produced by Opx barometry (McGregor , 1974) was transformed (Ashchepkov et al ., 2004; 2010; 2011) to satisfy the increasing data bases for the mantle xenoliths and experimental values 530 in peridotitic and 650 in elcogitic systems . The obtained difference Pd =Pcpx- Pexp were studied for the dependence on each component and their combination . Instead of the common activities we used the temperature-dependent empirical equations. The three separate equations for the common peridotites, pyroxenites and eclogites (Ashchepkov et al., 2010) were checked and complex To and Al-Na-Fe dependent universal coefficients were received. The KD is determined as follows: KD=Na/AlCr*Mg/Ca The logarithmic dependence between P and KD was transformed to a linear one. Final pressure equations are: AlCr=(Al-0.01) *((T-600)/700)**0.75+Cr*(ToK-100)/1000+(4*Ti-0.0125)/ (T0-801)*650 +0.55*((Fe-0.23) *(T0-900)/10000-K) P=0.26*(5+12*(Al+0.30*Na)KD* ToK**0.75 /(1+Fe+ Fe*(ToK-600)/1000)-ln(1273/ ToK))*40*(7*Na-Al-15*Ti+10*Cr+Mg/4)+7.5*Si-20*( Al*Na*Mg/Ca/(Al-2*Ti+Na-2*Fe/(Fe+Mg))+50*(Na+0.1*Al-2*Ti+0.05*Mg-0.22*Ca-0.7*Na)/Ca). Obtained equation in combination with the (Nimis,Taylor, 2000) thermometer allow to reconstruct position of the magma feeder systems of the alkali basaltic magma withing the mantle diapirs in modern platforms like in Vitim plateau (Ashchepkov et al., 2011) and now was applicated to reconstruct the deep seated magma conduits beneath the mountain collision systems, island arcs ocean plateaus etc. This equation allows to receive the positions of the major groups of eclogites mantle sections and to find out the regularities of their behavior. The Fe rich eclogites commonly

Highly refractory Archaean peridotite cumulates: Petrology and geochemistry of the Seqi Ultramafic Complex, SW Greenland

Directory of Open Access Journals (Sweden)

Kristoffer Szilas

2018-05-01

Full Text Available This paper investigates the petrogenesis of the Seqi Ultramafic Complex, which covers a total area of approximately 0.5 km2. The ultramafic rocks are hosted by tonalitic orthogneiss of the ca. 3000 Ma Akia terrane with crosscutting granitoid sheets providing an absolute minimum age of 2978 ± 8 Ma for the Seqi Ultramafic Complex. The Seqi rocks represent a broad range of olivine-dominated plutonic rocks with varying modal amounts of chromite, orthopyroxene and amphibole, i.e. various types of dunite (s.s., peridotite (s.l., as well as chromitite. The Seqi Ultramafic Complex is characterised primarily by refractory dunite, with highly forsteritic olivine with core compositions having Mg# ranging from about 91 to 93. The overall high modal contents, as well as the specific compositions, of chromite rule out that these rocks represent a fragment of Earth's mantle. The occurrence of stratiform chromitite bands in peridotite, thin chromite layers in dunite and poikilitic orthopyroxene in peridotite instead supports the interpretation that the Seqi Ultramafic Complex represents the remnant of a fragmented layered complex or a magma conduit, which was subsequently broken up and entrained during the formation of the regional continental crust.Integrating all of the characteristics of the Seqi Ultramafic Complex points to formation of these highly refractory peridotites from an extremely magnesian (Mg# ∼ 80, near-anhydrous magma, as olivine-dominated cumulates with high modal contents of chromite. It is noted that the Seqi cumulates were derived from a mantle source by extreme degrees of partial melting (>40%. This mantle source could potentially represent the precursor for the sub-continental lithospheric mantle (SCLM in this region, which has previously been shown to be ultra-depleted. The Seqi Ultramafic Complex, as well as similar peridotite bodies in the Fiskefjord region, may thus constitute the earliest cumulates that formed during the

High energy density layered-spinel hybrid cathodes for lithium ion rechargeable batteries

Energy Technology Data Exchange (ETDEWEB)

Basu, S., E-mail: sbasumajumder@yahoo.com [Department of Physics, Indian Institute of Technology Kharagpur, Kharagpur 721 302 (India); Dahiya, P.P.; Akhtar, Mainul [Materials Science Center, Indian Institute of Technology Kharagpur, Kharagpur 721 302 (India); Ray, S.K. [Department of Physics, Indian Institute of Technology Kharagpur, Kharagpur 721 302 (India); Chang, J.K. [Institute of Materials Science and Engineering, National Central University, Taiwan (China); Majumder, S.B. [Materials Science Center, Indian Institute of Technology Kharagpur, Kharagpur 721 302 (India)

2016-11-15

Highlights: • Structural integration of layered domains in spinel matrix of the composite particles. • Highest discharge capacity (275 mAh g{sup −1}) in composite with 30.0 mole% Li{sub 2}MnO{sub 3}. • Reasonably good rate capability of layered-spinel composite cathode. • Capacity fading with cycling is related to cubic to tetragonal structural phase transition. - Abstract: High energy density Li{sub 2}MnO{sub 3} (layered)–LiMn{sub 1.5}Ni{sub 0.5}O{sub 4} (spinel) composite cathodes have been synthesized using auto-combustion route. Rietveld refinements together with the analyses of high resolution transmission electron micrographs confirm the structural integration of Li{sub 2}MnO{sub 3} nano-domains into the LiMn{sub 1.5}Ni{sub 0.5}O{sub 4} matrix of the composite cathodes. The discharge capacity of the composite cathodes are due to the intercalation of Li{sup +} ion in the tetrahedral (8a) and octahedral (16c) sites of the spinel component and also the insertion of Li{sup +} in the freshly prepared MnO{sub 2} lattice, formed after Li{sub 2}O extraction from the Li{sub 2}MnO{sub 3} domains. The capacity fading of the composite cathodes are explained to be due to the layered to spinel transition of the Li{sub 2}MnO{sub 3} component and Li{sup +} insertion into the octahedral site of the spinel lattices which trigger cubic to tetragonal phase transition resulting volume expansion which eventually retard the Li{sup +} intercalation with cycling.

Widespread melt/rock interaction and seismic properties of the lithosphere above mantle plumes: Evidence from mantle xenoliths from French Polynesia

Science.gov (United States)

Tommasi, A.; Godard, M.; Coromina, G.; Dautria, J. M.; Barczus, H.

2003-04-01

In addition to thermal erosion, plume/lithosphere interaction may induce significant changes in the lithosphere chemical composition. To constrain the extent of this process in an oceanic environment and its consequences on the lithosphere seismic properties, we studied the relationship between petrological processes and microstructure in mantle xenoliths from the Austral-Cook, Society and Marquesas islands. Olivine forsterite contents in our sp-peridotites vary continuously from Fo91 to Fo83, the lowest Fo being observed in dunites and wehrlites. Yet, their high Ni content (up to 2500 ppm) precludes a cumulate origin. These rocks are rather interpreted as resulting from melt/rock reactions involving olivine precipitation and pyroxene dissolution, the dunites indicating high melt-rock ratios. Moreover, wehrlites display poikiloblastic diopside enclosing corroded olivines. Late crystallization of clinopyroxene, also observed in lherzolites, may result from a near-solidus melt-freezing reaction occurring at the boundary of a partial melting domain developed at the expenses of lithospheric mantle. These data suggest that the lithosphere above a mantle plume undergoes a complex sequence of magmatic processes that significantly change its composition. Yet, crystal preferred orientations and thus seismic anisotropy are little affected by these processes. Lherzolites and harzburgites, independent from composition, show high-temperature porphyroclastic microstructures and strong olivine CPO. Although dunites and wehrlites display annealing microstructures to which is associated a progressive dispersion of the olivine CPO, very weak CPO are limited to a few dunites and wehrlites, suggesting that CPO destruction is restricted to domains of intense magma-rock interaction due to localized flow or accumulation of magmas. Conversely, the compositional changes result in lower seismic velocities for P- and S-waves. Relative to normal mantle, seismic anomalies may attain -2.5 (2

Water Distribution in the Continental and Oceanic Upper Mantle

Science.gov (United States)

Peslier, Anne H.

2015-01-01

Nominally anhydrous minerals such as olivine, pyroxene and garnet can accommodate tens to hundreds of ppm H2O in the form of hydrogen bonded to structural oxygen in lattice defects. Although in seemingly small amounts, this water can significantly alter chemical and physical properties of the minerals and rocks. Water in particular can modify their rheological properties and its distribution in the mantle derives from melting and metasomatic processes and lithology repartition (pyroxenite vs peridotite). These effects will be examined here using Fourier transform infrared spectrometry (FTIR) water analyses on minerals from mantle xenoliths from cratons, plume-influenced cratons and oceanic settings. In particular, our results on xenoliths from three different cratons will be compared. Each craton has a different water distribution and only the mantle root of Kaapvaal has evidence for dry olivine at its base. This challenges the link between olivine water content and survival of Archean cratonic mantle, and questions whether xenoliths are representative of the whole cratonic mantle. We will also present our latest data on Hawaii and Tanzanian craton xenoliths which both suggest the intriguing result that mantle lithosphere is not enriched in water when it interacts with melts from deep mantle upwellings (plumes).

Znx-1CuxMn2O4 spinels; synthesis, structural characterization and electrical evaluation

International Nuclear Information System (INIS)

Mendez M, F.; Lima, E.; Bosch, P.; Pfeiffer, H.; Gonzalez, F.

2010-01-01

This work presents the structural characterization and electrical evaluation of Zn x-1 Cu x Mn 2 O 4 spinels, which are materials presented as secondary phases into the vari stor ceramic systems. Samples were analyzed by X-ray diffraction, solid-state nuclear magnetic resonance, infrared spectroscopy, scanning electron microscopy and impedance spectroscopy. Although, the addition of copper to the ZnMn 2 O 4 spinel did not produce morphological changes, the structure and electrical behaviors changed considerably. Structurally, copper addition induced the formation of partial inverse spinels, and its addition increases significantly the electrical conductivity. Therefore, the formation of Zn x-1 Cu x Mn 2 O 4 spinels, as secondary phases into the vari stor materials, may compromise significantly the vari stor efficiency. (Author)

Ancient mantle in a modern arc: osmium isotopes in izu-bonin-mariana forearc peridotites

Science.gov (United States)

Parkinson; Hawkesworth; Cohen

1998-09-25

Mantle peridotites drilled from the Izu-Bonin-Mariana forearc have unradiogenic 187Os/188Os ratios (0.1193 to 0.1273), which give Proterozoic model ages of 820 to 1230 million years ago. If these peridotites are residues from magmatism during the initiation of subduction 40 to 48 million years ago, then the mantle that melted was much more depleted in incompatible elements than the source of mid-ocean ridge basalts (MORB). This result indicates that osmium isotopes record information about ancient melting events in the convecting upper mantle not recorded by incompatible lithophile isotope tracers. Subduction zones may be a graveyard for ancient depleted mantle material, and portions of the convecting upper mantle may be less radiogenic in osmium isotopes than previously recognized.

Three types of element fluxes from metabasite into peridotite in analogue experiments: Insights into subduction-zone processes

Science.gov (United States)

Perchuk, A. L.; Yapaskurt, V. O.; Griffin, W. L.; Shur, M. Yu.; Gain, S. E. M.

2018-03-01

Piston-cylinder experiments with natural rocks and mineral separates were carried out at 750-900 °C and 2.9 GPa, conditions relevant to hot subduction zones, to study the mechanisms of metasomatic alteration of mantle-wedge rocks such as dunite and lherzolite, and the transfer of trace elements released from a carbonate-bearing amphibolite during its eclogitization. Element transfer from the slab to the mantle lithologies occurred in porous-, focused- and diffusive-flow regimes that remove melt and carbon, and partially water, from the metabasite layer. Porous flow is recorded by dissolution of clinopyroxene and growth of orthopyroxene ± garnet ± magnesite ± chlorite along grain boundaries in the peridotite layers, but is invisible in the metabasite layers. Porous flow of the same fluids/melts produces harzburgite mineralogy in both dunite and lherzolite. The transformation of lherzolite to harzburgite reflects breakdown of clinopyroxene in the lherzolite and diffusion of the liberated calcium into the metabasite layer, i.e. against the direction of major fluid/melt flow. Focused flow develops along the side walls of the capsules, producing a melt-free omphacite ± phengite ± quartz paragenesis in the metabasite, and melt segregations, separated from the host peridotite layers by newly-formed omphacite ± garnet ± phlogopite + orthopyroxene + magnesite. Diffusive flow leads to the formation of orthopyroxene ± magnesite ± garnet reaction zones at the metabasite-peridotite interface and some melt-peridotite interfaces. Melt segregations in the peridotite layers at 850-900 °C are rich in LREE and LILE, strongly depleted in Y and HREE, and have higher Sr/Y and La/Yb ratios than island arc andesites, dacites and rhyolites. These features, and negative anomalies in Nb-Ta and low Nb/Ta, resemble those of high-silica adakites and TTGs, but K2O is high compared to TTGs. Metasomatism in the dunite layer changes the REE patterns of dunite, recording chromatographic

Exploring Lithium-Cobalt-Nickel Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells

Energy Technology Data Exchange (ETDEWEB)

Lee, Eungje; Blauwkamp, Joel; Castro, Fernando C.; Wu, Jinsong; Dravid, Vinayak P.; Yan, Pengfei; Wang, Chongmin; Kim, Soo; Wolverton, Christopher; Benedek, Roy; Dogan, Fulya; Park, Joong Sun; Croy, Jason R.; Thackeray, Michael M.

2016-10-19

Recent reports have indicated that a manganese oxide spinel component, when embedded in a relatively small concentration in layered xLi2MnO3(1-x)LiMO2 (M=Ni, Mn, Co) electrode systems, can act as a stabilizer that increases their capacity, rate capability, cycle life, and first-cycle efficiency. These findings prompted us to explore the possibility of exploiting lithiated cobalt oxide spinel stabilizers by taking advantage of (1) the low mobility of cobalt ions relative to manganese and nickel ions in close-packed oxides and (2) their higher potential (~3.6 V vs. Li0) relative to manganese oxide spinels (~2.9 V vs. Li0) for the spinel-to-lithiated spinel electrochemical reaction. In particular, we have revisited the structural and electrochemical properties of lithiated spinels in the LiCo1-xNixO2 (0x0.2) system, first reported almost 25 years ago, by means of high-resolution (synchrotron) X-ray diffraction, transmission electron microscopy, nuclear magnetic resonance spectroscopy, electrochemical cell tests, and theoretical calculations. The results provide a deeper understanding of the complexity of intergrown layered/lithiated spinel LiCo1-xNixO2 structures, when prepared in air between 400 and 800 C, and the impact of structural variations on their electrochemical behavior. These structures, when used in low concentration, offer the possibility of improving the cycling stability, energy, and power of high energy (≥3.5 V) lithium-ion cells.

Spin Filtering in Epitaxial Spinel Films with Nanoscale Phase Separation

KAUST Repository

Li, Peng

2017-05-08

The coexistence of ferromagnetic metallic phase and antiferromagnetic insulating phase in nanoscaled inhomogeneous perovskite oxides accounts for the colossal magnetoresistance. Although the model of spin-polarized electron transport across antiphase boundaries has been commonly employed to account for large magnetoresistance (MR) in ferrites, the magnetic anomalies, the two magnetic phases and enhanced molecular moment, are still unresolved. We observed a sizable MR in epitaxial spinel films (NiCo2O4-δ) that is much larger than that commonly observed in spinel ferrites. Detailed analysis reveals that this MR can be attributed to phase separation, in which the perfect ferrimagnetic metallic phase and ferrimagnetic insulating phase coexist. The magnetic insulating phase plays an important role in spin filtering in these phase separated spinel oxides, leading to a sizable MR effect. A spin filtering model based on Zeeman effect and direct tunneling is developed to account for MR of the phase separated films.

Water-Rock Interactions in the Peridotite Aquifer of the Oman-UAE Ophiolite: Strontium Isotopic Ratio and Geochemical Evolution of Groundwater

Science.gov (United States)

Bompard, Nicolas; Matter, Juerg; Teagle, Damon

2016-04-01

The peridotite aquifer in Wadi Tayin, Sultanate of Oman, is a perfect example of natural carbonation of ultramafic rocks. In situ mineral carbonation is considered the most safest and permanent option of CO2 Capture and Sequestration (CCS). However, the process itself is yet to be characterised and a better understanding of the mechanisms involved in natural mineral carbonation is needed before geo-engineering it. We used the 87Sr/86Sr system to follow the water-rock interactions along the groundwater flowpath in the peridotite aquifer and to determine the sources of divalent cations (Mg2+, Ca2+) required for mineral carbonation. The Sr-isotope data of groundwater show that the aquifer rocks are the main source for divalent cations (Mg2+, Ca2+ and Sr2+) and secondary carbonates are their main sink. The groundwater 87Sr/86Sr ratio evolves with its pH: from 87Sr/86Sr = 0.7087 (n=3) to 0.7082 (n=8) between pH 7 and 8, and from 0.7086 (n=6) at pH 9 to 0.07075 (n=9) at pH 11. This evolution seems to support a two-step model for the water-rock interactions in the peridotite aquifer. From pH 7 to 8, secondary Ca-carbonate precipitation buffers the pH rise resulting from peridotite serpentinisation. From pH 9 to 11, peridotite serpentinisation drives the pH to alkaline condition. The change from a Mg-rich to a Ca-rich groundwater at pH 9 seems to confirm the two-step model.

Sediment-peridotite interactions in a thermal gradient: mineralogic and geochemical effects and the "sedimentary signature" of arc magmas

Science.gov (United States)

Woodland, Alan; Girnis, Andrei; Bulatov, Vadim; Brey, Gerhard; Höfer, Heidi; Gerdes, Axel

2017-04-01

Strong thermal and chemical gradients are characteristic of the slab-mantle interface in subduction zones where relatively cold sediments become juxtaposed with hotter peridotite of the mantle wedge. The formation of arc magmas is directly related to mass transfer processes under these conditions. We have undertaken a series of experiments to simulate interactions and mass transfer at the slab-mantle interface. In addition to having juxtaposed sediment and peridotite layers, the experiments were performed under different thermal gradients. The sediment had a composition similar to GLOSS (1) and also served as the source of H2O, CO2 and a large selection of trace elements. The peridotite was a depleted garnet harzburgite formed from a mixture of natural hand-picked olivine, opx and garnet. Graphite was added to this mixture to establish a redox gradient between the two layers. Experiments were performed at 7.5-10 GPa to simulate the processes during deep subduction. The thermal gradient was achieved by displacing the sample capsule (Re-lined Pt) from the center of the pressure cell. The gradient was monitored with separate thermocouples at each end of the capsule and by subsequent opx-garnet thermometry across the sample. Maximum temperatures varied from 1400˚ -900˚ C and gradients ranged from 200˚ -800˚ C. Thus, in some experiments melting occurred in the sediment layer and in others this layer remained subsolidus, only devolatilizing. Major and trace elements were transported both in the direction of melt percolation to the hot zone, as well as down temperature. This leads to the development of zones with discrete phase assemblages. Olivine in the peridotite layer becomes converted to orthopyroxene, which is due to Si addition, but also migration of Mg and Fe towards the sediment. In the coldest part of a sample, the sediment is converted into an eclogitic cpx + garnet assemblage. A thin zone depleted in almost all trace elements is formed in peridotite

The production of iron oxide during peridotite serpentinization: Influence of pyroxene

Directory of Open Access Journals (Sweden)

Ruifang Huang

2017-11-01

Full Text Available Serpentinization produces molecular hydrogen (H2 that can support communities of microorganisms in hydrothermal fields; H2 results from the oxidation of ferrous iron in olivine and pyroxene into ferric iron, and consequently iron oxide (magnetite or hematite forms. However, the mechanisms that control H2 and iron oxide formation are poorly constrained. In this study, we performed serpentinization experiments at 311 °C and 3.0 kbar on olivine (with <5% pyroxene, orthopyroxene, and peridotite. The results show that serpentine and iron oxide formed when olivine and orthopyroxene individually reacted with a saline starting solution. Olivine-derived serpentine had a significantly lower FeO content (6.57 ± 1.30 wt.% than primary olivine (9.86 wt.%, whereas orthopyroxene-derived serpentine had a comparable FeO content (6.26 ± 0.58 wt.% to that of primary orthopyroxene (6.24 wt.%. In experiments on peridotite, olivine was replaced by serpentine and iron oxide. However, pyroxene transformed solely to serpentine. After 20 days, olivine-derived serpentine had a FeO content of 8.18 ± 1.56 wt.%, which was significantly higher than that of serpentine produced in olivine-only experiments. By contrast, serpentine after orthopyroxene had a slightly higher FeO content (6.53 ± 1.01 wt.% than primary orthopyroxene. Clinopyroxene-derived serpentine contained a significantly higher FeO content than its parent mineral. After 120 days, the FeO content of olivine-derived serpentine decreased significantly (5.71 ± 0.35 wt.%, whereas the FeO content of orthopyroxene-derived serpentine increased (6.85 ± 0.63 wt.% over the same period. This suggests that iron oxide preferentially formed after olivine serpentinization. Pyroxene in peridotite gained some Fe from olivine during the serpentinization process, which may have led to a decrease in iron oxide production. The correlation between FeO content and SiO2 or Al2O3 content in olivine- and

Chemical synthesis of nanocrystalline magnesium aluminate spinel via nitrate-citrate combustion route

International Nuclear Information System (INIS)

Saberi, Ali; Golestani-Fard, Farhad; Sarpoolaky, Hosein; Willert-Porada, Monika; Gerdes, Thorsten; Simon, Reinhard

2008-01-01

Nanocrystalline magnesium aluminate spinel (MgAl 2 O 4 ) was synthesized using metal nitrates, citric acid and ammonium solutions. The precursor and the calcined powders at different temperatures were characterized by X-ray diffraction (XRD), simultaneous thermal analysis (STA), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The combustion mechanism was also studied by a quadrupole mass spectrometer (QMS) which coupled to STA. The generated heat through the combustion of the mixture of ammonium nitrate and citrate based complexes decreased the synthesis temperature of MgAl 2 O 4 spinel. The synthesized MgAl 2 O 4 spinel at 900 deg. C has faced shape with crystallite size in the range of 18-24 nm

Origin of spinel lamella and/or inclusions in olivine of harzburgite form the Pauza ultramafic rocks from the Kurdistan region, northeastern Iraq

Science.gov (United States)

Mohammad, Y.; Maekawa, H.; Karim, K.

2009-04-01

Exsolution lamellae and octahedral inclusions of chromian spinel occur in olivine of harzburgite of the Pauza ultramafic rocks, Kurdistan region, northeastern Iraq. The lamella is up to 80μm long and up to 50 μm wide. The lamellae and octahedral inclusions of chromian spinel are distributed heterogeneously in the host olivine crystal. They are depleted in Al2O3 relative to the subhedral spinel grains in the matrix and spinel lamella in orthopyroxene. Olivine (Fo92 - 93) with spinel lamellae occurs as fine-grained crystals around orthopyroxene, whereas olivine (Fo90-91) free from spinel is found in matrix. Based on back-scattered images analyses, enrichments of both Cr # and Fe+3 in the chromian spinel lamella in olivine (replacive olivine) relative to that in adjacent orthopyroxene. As well as the compositions of chromian spinel lamellae host olivine are more Mg-rich than the matrix olivine. Furthermore the restriction of olivine with spinel lamellae and octahedral inclusions on around orthopyroxene, and the similarity of spinel lamella orientations in both olivine and adjacent orthopyroxene. This study concludes that the spinel inclusions in olivine are remnant (inherited from former orthopyroxene) spinel exsolution lamella in orthopyroxene, that has been formed in upper mantle conditions ( T = 1200 °C, P = 2.5 GPa ). Replacive olivine are formed by reaction of ascending silica poor melt and orthopyroxene in harzburgite as pressure decrease the solubility of silica-rich phase (orthopyroxene) in the system increase, therefore ascending melt dissolve pyroxene with spinel exsolution lamella and precipitate replacive olivine with spinel inclusions. We can conclude that the olivines with spinel lamella are not necessary to be original and presenting ultrahigh-pressure and/or ultra deep-mantle conditions as previously concluded. It has been formed by melting of orthopyroxene (orthopyroxene with spinel exsolution lamella = olivine with spinel lamellae and octahedral

On the use of spinel-based nuclear fuels for the transmutation of actinides

International Nuclear Information System (INIS)

Konings, R.J.M.; Bakker, K.; Boshoven, J.G.; Hein, H.; Huntelaar, M.E.; Zhang, H.; Meeldijk, J.D.; Woensdregt, C.F.

1997-01-01

The properties of spinel-based nuclear fuels for the transmutation of actinides are investigated. The results of laboratory experiments, thermodynamic calculations and irradiations in the High Flux Reactor (HFR) at Petten are presented, and allow us to evaluate the potential of spinel as an inert matrix for fuels and targets for transmutation. (author)

Characterization of Spitsbergen Disks by Transmission Electron Microscopy and Raman Spectroscopy

Science.gov (United States)

Thomas-Keprta, K. L.; Clemett, S. J.; Le, L.; Ross, K.; McKay, David S.; Gibson, E. K., Jr.

2010-01-01

'Carbonate disks' found in the fractures and pores spaces of peridotite xenoliths and basalts from the island of Spitsbergen in the Norwegian Svalbard archipelago have been suggested to be "The best (and best documented) terrestrial analogs for the [Martian meteorite] ALH84001 carbonate globules ..." Previous studies have indicated that Spitsbergen carbonates show broadly comparable internal layering and mineral compositions to ALH84001 carbonate-magnetite disks. We report here for the first time, the detailed mineral characterization of Spitsbergen carbonates and their spatial relationship to the host mineral assemblages in the xenolith, using high resolution TEM (as used previously for ALH84001 carbonate disks). These studies were conducted in concert with complementary Raman and SEM analysis of the same samples. Our results indicate that there are significant chemical and physical differences between the disks in Spitsbergen and the carbonates present in ALH84001.

The force of crystallization and fracture propagation during in-situ carbonation of peridotite

NARCIS (Netherlands)

van Noort, Reinier; Wolterbeek, Timotheus K.T.; Drury, Martyn R.; Kandianis, Michael T.; Spiers, Christopher J.

2017-01-01

Subsurface mineralization of CO2 by injection into (hydro-)fractured peridotites has been proposed as a carbon sequestration method. It is envisaged that the expansion in solid volume associated with the mineralization reaction leads to a build-up of stress, resulting in the opening of further

Formation and temporal evolution of the Kalahari sub-cratonic lithospheric mantle: Constraints from Venetia xenoliths, South Africa

NARCIS (Netherlands)

Hin, R.C.; Morel, M.L.A.; Nebel, O.; Mason, P.R.D.; van Westrenen, W.; Davies, G.R.

2009-01-01

The ~533 Ma Venetia Diamond Mine is located between the Kaapvaal and Zimbabwe Cratons and the study of selected xenoliths provides the opportunity to investigate the temporal evolution of the sub-continental lithospheric mantle (SCLM) underneath southern Africa, as well as the extent and potentially

Magnetic behavior of the oxide spinels

Indian Academy of Sciences (India)

... Refresher Courses · Symposia · Live Streaming. Home; Journals; Pramana – Journal of Physics; Volume 58; Issue 5-6. Magnetic behavior of the oxide spinels: Li0.5Fe2.5-2AlCrO4. U N Trivedi K B Modi H H Joshi. Colossal Magnetoresistance & Other Materials Volume 58 Issue 5-6 May-June 2002 pp 1031-1034 ...

Chromian spinels in highly altered ultramafic rocks from the Sartohay ophiolitic mélange, Xinjiang, NW China

Science.gov (United States)

Qiu, Tian; Zhu, Yongfeng

2018-06-01

The Sartohay ophiolitic mélange is located in western Junggar (Xinjiang province, NW China), which is a major component of the core part of the Central Asian Orogenic Belt (CAOB). Chromian spinels in serpentinite, talc schist, carbonate-talc schist and listwaenite in Sartohay ophiolitic mélange retain primary compositions with Cr# of 0.39-0.65, Mg# = 0.48-0.67, and Fe3+# evolution of chromian spinels in highly altered ultramafic rocks from the Sartohay ophiolitic mélange. Chromian spinels in serpentinite and talc schist were rimmed by Cr-magnetite, which was dissolved completely during transformation from serpentinite/talc schist to listwaenite. Chromian spinels were then transformed into Fe2+-rich chromite in shear zones, which characterized by high fluid/rock ratios. This Fe2+-rich chromite and/or chromian spinels could then be transformed into Fe3+-rich chromite in oxidizing conditions at shallow levels.

MgAl2O4 spinel refractory as containment liner for high-temperature alkali salt containing environments

Science.gov (United States)

Peascoe-Meisner, Roberta A [Knoxville, TN; Keiser, James R [Oak Ridge, TN; Hemric, James G [Knoxville, TN; Hubbard, Camden R [Oak Ridge, TN; Gorog, J Peter [Kent, WA; Gupta, Amul [Jamestown, NY

2008-10-21

A method includes containing a high-temperature alkali salt containing environment using a refractory containment liner containing MgAl.sub.2O.sub.4 spinel. A method, includes forming a refractory brick containing MgAl.sub.2O.sub.4 spinel having an exterior chill zone defined by substantially columnar crystallization and an interior zone defined by substantially equiaxed crystallization; and removing at least a portion of the exterior chill zone from the refractory brick containing MgAl.sub.2O.sub.4 spinel by scalping the refractory brick containing MgAl.sub.2O.sub.4 spinel to define at least one outer surface having an area of substantially equiaxed crystallization. A product of manufacture includes a refractory brick containing MgAl.sub.2O.sub.4 spinel including an interior zone defined by substantially equiaxed crystallization; and at least one outer surface having an area of substantially equiaxed crystallization.

Isotope geochemistry of xenoliths from East Africa. Implications for development of mantle reservoirs and their interaction

Energy Technology Data Exchange (ETDEWEB)

Cohen, R S; O' Nions, R K [Cambridge Univ. (UK). Dept. of Earth Sciences; Dawson, J B [Sheffield Univ. (UK). Dept. of Geology

1984-05-01

Pd, Nd and Sr isotope analyses together with U, Pb, Sm, Nd, Rb and Sr concentrations have been obtained for separated phases of lherzolite and bulk rock mafic granulite xenoliths in Recent volcanics from Tanzania. A garnet lherzolite from the Lashaine vent has yielded the least radiogenic Pb (/sup 206/Pb//sup 204/PB=15.55) and Nd (/sup 143/Nd//sup 144/Nd=0.51127; epsilon/sup 0/sub(Nd)=-26.7) isotope compositions recorded so far for an ultramafic xenolith, and /sup 87/Sr//sup 86/Sr=0.83604. The Pb isotope compositions of the mafic granulites are variable 15.77xenoliths do not conform with those of MORB, particularly in terms of their Pb-Sr, and Nd-Pb relationship. In this regard they are similar to some ocean islands and could be a viable source material for some ocean island basalts at least. The mantle part of the continental lithosphere is as likely to contain recycled components derived from the continental crust as are other regions of mantle. If the mantle part of continental lithosphere is invoked as a source for ocean islands, it does not negate the possibility that substantial recycled components are involved.

Origin of the low compressibility in hard nitride spinels

DEFF Research Database (Denmark)

Mori-Sánchez, P.; Marqués, M.; Beltrán, A.

2003-01-01

A microscopic investigation of first-principles electron densities of gamma-A(3)N(4) (A:C,Si,Ge) spinels reveals a clear relationship between the compressibility and the chemical bonding of these materials. Three striking findings emanate from this analysis: (i) the chemical graph is governed...... by a network of highly directional strong bonds with covalent character in gamma-C3N4 and different degrees of ionic polarization in gamma-Si3N4 and gamma-Ge3N4, (ii) nitrogen is the lowest compressible atom controlling the trend in the bulk modulus of the solids, and (iii) the group-IV counterions show strong...... site dependent compressibilities enhancing the difficulty in the synthesis of the spinel phases of these nitrides....

Cation-substituted spinel oxide and oxyfluoride cathodes for lithium ion batteries

Science.gov (United States)

Manthiram, Arumugam; Choi, Wonchang

2010-05-18

The present invention includes compositions and methods of making cation-substituted and fluorine-substituted spinel cathode compositions by firing a LiMn2-y-zLiyMzO4 oxide with NH4HF2 at low temperatures of between about 300 and 700.degree. C. for 2 to 8 hours and a .eta. of more than 0 and less than about 0.50, mixed two-phase compositions consisting of a spinel cathode and a layered oxide cathode, and coupling them with unmodified or surface modified graphite anodes in lithium ion cells.

Boron Isotopic Composition of Metasomatized Mantle Xenoliths from the Western Rift, East Africa

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Hudgins, T.; Nelson, W. R.

2017-12-01

The Western Branch of the East African Rift System is known to have a thick lithosphere and sparse, alkaline volcanism associated with a metasomatized mantle source. Recent work investigating the relationship between Western Branch metasomatized mantle xenoliths and associated lavas has suggested that these metasomes are a significant factor in the evolution of the rift. Hydrous/carbonated fluids or silicate melts are potent metasomatic agents, however gaining insight into the source of a metasomatic agent proves challenging. Here we investigate the potential metasomatic fluid sources using B isotope analysis of mineral separates from Western Branch xenoliths. Preliminary SIMS analyses of phlogopite from Katwe Kikorongo and Bufumbira have and average B isotopic composition of -28.2‰ ± 5.1 and -16.4‰ ± 3.6, respectively. These values are are dissimilar to MORB (-7.5‰ ± 0.7; Marschall and Monteleone, 2015), primitive mantle (-10‰ ± 2; Chaussidon and Marty, 1995), and bulk continental crust (-9.1‰ ± 2.4; Marschall et al., 2017) and display significant heterogeneity across a relatively short ( 150km) portion of the Western Branch. Though displaying large variability, these B isotopic compositions are indicative of a metasomatic agent with a more negative B isotopic composition than MORB, PM, or BCC. These results are consistent with fluids that released from a subducting slab and may be related to 700 Ma Pan-African subduction.

Spinels as cathodes for the electrochemical reduction of O2 and NO

DEFF Research Database (Denmark)

Simonsen, Vibe Louise Ernlund; Find, D.; Lilliedal, M.

2007-01-01

the largest difference in activity between reduction of oxygen and the reduction of nitric oxide, the activity being highest for the reduction of nitric oxide. The material is probably not stable when polarised cathodically. However it seems that the electrode material can be regenerated upon oxidation. NiFe2......Spinels were synthesised and investigated as electro-catalyst for the electrochemical reduction of oxygen and nitric oxide using cyclic voltammetry and cone shaped electrodes. The following four spinels were investigated; CoFe2O4, NiFe2O4, CuFe2O4 and Co3O4. The composition CuFe2O4 revealed......O4 is also more active for the reduction of nitric oxide than for the reduction of oxygen, whereas the cobalt containing spinels have a higher activity for the reduction of oxygen than for the reduction of nitric oxide....

Nanodiamond finding in the hyblean shallow mantle xenoliths.

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Simakov, S K; Kouchi, A; Mel'nik, N N; Scribano, V; Kimura, Y; Hama, T; Suzuki, N; Saito, H; Yoshizawa, T

2015-06-01

Most of Earth's diamonds are connected with deep-seated mantle rocks; however, in recent years, μm-sized diamonds have been found in shallower metamorphic rocks, and the process of shallow-seated diamond formation has become a hotly debated topic. Nanodiamonds occur mainly in chondrite meteorites associated with organic matter and water. They can be synthesized in the stability field of graphite from organic compounds under hydrothermal conditions. Similar physicochemical conditions occur in serpentinite-hosted hydrothermal systems. Herein, we report the first finding of nanodiamonds, primarily of 6 and 10 nm, in Hyblean asphaltene-bearing serpentinite xenoliths (Sicily, Italy). The discovery was made by electron microscopy observations coupled with Raman spectroscopy analyses. The finding reveals new aspects of carbon speciation and diamond formation in shallow crustal settings. Nanodiamonds can grow during the hydrothermal alteration of ultramafic rocks, as well as during the lithogenesis of sediments bearing organic matter.

Single-crystalline MgAl2O4 spinel nanotubes using a reactive and removable MgO nanowire template

International Nuclear Information System (INIS)

Fan Hongjin; Knez, Mato; Scholz, Roland; Nielsch, Kornelius; Pippel, Eckhard; Hesse, Dietrich; Goesele, Ulrich; Zacharias, Margit

2006-01-01

Using MgO nanowires as a reactive template, we fabricated for the first time single-crystal MgAl 2 O 4 spinel nanotubes through an interfacial solid-state reaction of MgO-Al 2 O 3 core-shell nanowires. Single-crystal MgO nanowires are coated with a conformal thin layer of amorphous Al 2 O 3 via atomic layer deposition. Subsequent annealing at 700 deg. C activates the interfacial reaction between MgO and Al 2 O 3 , transforming the alumina shell into a spinel shell. Finally, after etching away the remaining MgO core in ammonia sulfuric solution, MgAl 2 O 4 spinel nanotubes are obtained. As a transition from conventional planar spinel layers via thin-film interface reactions, our result might open a window for the fabrication of a wide variety of MgO-based spinel one-dimensional nanostructures

Depleted subcontinental lithospheric mantle and its tholeiitic melt metasomatism beneath NE termination of the Eger Rift (Europe): the case study of the Steinberg (Upper Lusatia, SE Germany) xenoliths

Science.gov (United States)

Kukuła, Anna; Puziewicz, Jacek; Matusiak-Małek, Magdalena; Ntaflos, Theodoros; Büchner, Jörg; Tietz, Olaf

2015-12-01

The ca. 30 Ma Steinberg basanite occurs at the NE termination of the Eger (Ohře) Rift in the NW Bohemian Massif, Central Europe, and belongs to the Cenozoic alkaline Central European Volcanic Province. The basanite hosts a suite of mantle xenoliths, most of which are harzburgites containing relatively magnesian olivine (Fo 90.5-91.6) and Al-poor (0.04-0.13 a pfu) orthopyroxene (mg# 0.90-0.92). Some of these harzburgites also contain volumetrically minor clinopyroxene (mg# 0.92-0.95, Al 0.03-0.13 a pfu) and have U-shaped LREE-enriched REE patterns. The Steinberg harzburgites are typical for the Lower Silesian - Upper Lusatian domain of the European subcontinental lithospheric mantle. They represent residual mantle that has undergone extensive partial melting and was subsequently affected by mantle metasomatism by mixed carbonatite-silicate melts. The Steinberg xenolith suite comprises also dunitic xenoliths affected by metasomatism by melt similar to the host basanite, which lowered the Fo content in olivine to 87.6 %. This metasomatism happened shortly before xenolith entrainment in the erupting lava. One of the xenoliths is a wehrlite (olivine Fo 73 %, clinopyroxene mg# 0.83-0.85, subordinate orthopyroxene mg# 0.76-0.77). Its clinopyroxene REE pattern is flat and slightly LREE-depleted. This wehrlite is considered to be a tholeiitic cumulate. One of the studied harzburgites contains clinopyroxene with similar trace element contents to those in wehrlite. This type of clinopyroxene records percolation of tholeiitic melt through harzburgite. The tholeiitic melt might be similar to Cenozoic continental tholeiites occurring in the Central European Volcanic Province (e.g., Vogelsberg, Germany).

Investigating the effects of abyssal peridotite alteration on Si, Mg and Zn isotopes

Science.gov (United States)

Savage, P. S.; Wimpenny, J.; Harvey, J.; Yin, Q.; Moynier, F.

2013-12-01

Around 1/3 of Earth's divergent ridge system is now classified as "slow" spreading [1], exposing ultramafic rocks (abyssal peridotites) at the seafloor. Such material is often highly altered by serpentinisation and steatisation (talc formation). It is crucial to understand such processes in order to access the original composition of the mantle, and to quantify any impact on ocean composition. Here we examine the effect of both serpentinisation and steatisation on Si, Mg and Zn isotopes. Hydrothermal alteration and seafloor weathering are both sources of oceanic Si [2] and weathering of abyssal peridotites is a source of oceanic Mg [3]; hence isotopic fractionation as a result of seafloor alteration could affect oceanic Si and Mg isotope composition. Zinc isotopes can provide complimentary information; the magnitude and direction of fractionation is highly dependent on complexing ligand [4] and can provide compositional information on the fluids driving metasomatism. For this study, two cores from the well-characterised abyssal peridotites recovered on ODP Leg 209 were examined [5]. Hole 1274a peridotites exhibit variable serpentinisation at ~200°C, whereas samples from Hole 1268a have been comprehensively serpentinised and then subsequently steatised to talc facies at ~350°C, by a low Mg/Si, low pH fluid. The Si, Mg and Zn isotope compositions of 1274a samples are extremely homogeneous, identical to that of pristine mantle rocks (BSE) i.e., serpentinisation at this locality was predominantly isochemical [5]. In contrast, samples from 1268a show greater isotopic variability. In all samples, Mg is enriched in the heavier isotopes relative to BSE, consistent with formation of isotopically heavy secondary phases [6]. For Si, serpentinised samples are slightly enriched in the lighter isotopes compared to BSE, again consistent with the behaviour of Si during formation of secondary phases [7]. Within the steatised samples, some exhibit enrichments in the lighter Si

Thermal decomposition of chromite spinel with chlorite admixture

Energy Technology Data Exchange (ETDEWEB)

Sanchez-Ramos, S. [Department of Analytical Chemistry, Faculty of Chemistry, University of Valencia, C/Doctor Moliner 50, 46100-Burjassot, Valencia (Spain); Escuela Superior de Ceramica, C/Ceramista A. Blat 22, 46940 Manises, Valencia (Spain); Domenech-Carbo, A. [Department of Analytical Chemistry, Faculty of Chemistry, University of Valencia, C/Doctor Moliner 50, 46100-Burjassot, Valencia (Spain); Gimeno-Adelantado, J.V. [Department of Analytical Chemistry, Faculty of Chemistry, University of Valencia, C/Doctor Moliner 50, 46100-Burjassot, Valencia (Spain)], E-mail: jose.v.gimeno@uv.es; Peris-Vicente, J.; Valle-Algarra, F.M. [Department of Analytical Chemistry, Faculty of Chemistry, University of Valencia, C/Doctor Moliner 50, 46100-Burjassot, Valencia (Spain)

2008-09-30

The behaviour of minerals in a South African chromite ore during the increasing of the temperature has been studied. Firstly, the changes produced during the ignition process have been examined by means of thermal and differential analysis (TGA-DTA) until 1200 deg. C. The characterization of the initial mineral and those obtained after heating at several temperatures in room atmosphere has been performed by X-ray diffraction (XRD). Moreover, voltammetric analyses have allowed to determine the variation of the iron oxidation degree in the studied materials. Light microscopy was applied to find more information about the different phases by their colour. During the heating, a wide range of complex exothermic and endothermic transformations take place. Decomposition compounds were identified, which were produced by heat decomposition, loss of structural water, element substitutions and oxygen absorptions and desorptions, caused mainly by the variation of the iron oxidation degree. The spinels of the chromite ore decompose in other spinels, with a partial change of the iron oxidation degree. From nearly 800 deg. C, chrome oxide (Cr{sub 2}O{sub 3}) comes off from the chromite forming another phase, and almost at 1000 deg. C, a slow decrease of weight was detected, caused among others to the formation of a magnetite phase. Simultaneously, the silicates undergo strong modifications, including decompositions and incorporation of iron (II) in their structure and producing other silicates stable at high temperatures, which modify the behaviour of the pure spinels. Moreover, at 1200 deg. C these silicates decompose to cristobalite (SiO{sub 2})

MARID-type Glimmerites from Kimberley, South Africa: Metasomes or high-pressure cumulates?

Science.gov (United States)

Förster, Michael W.; Prelevic, Dejan; Buhre, Stephan; Jacob, Dorrit E.

2015-04-01

Mica- amphibole- rutile- ilmenite- diopside (MARID) xenoliths are alkali-rich, coarse-grained ultramafic rocks, typical for heavily metasomatized subcontinental lithospheric mantle (Dawson & Smith, 1977). They are produced either by interaction of mantle wall rock with lamproitic melts that percolate through the mantle (Dawson and Smith 1977; Sweeney 1993), or as direct crystallization products of those melts (Waters 1987). Two rock samples of mica-rich (>90% phlogopite) xenoliths from the Boshof Road Dump of the Bultfontein kimberlite diamond mine in Kimberley, South Africa were analyzed for major and trace elements of minerals. Millimeter sized phlogopite is the dominant mineral, making up more than 90% of the rock. Other phases are in descending order: diopside, K-richterite, rutile and ilmenite. Phlogopite is homogenous in composition and appears without zonation. They are perpotassic with K/Al between 1.1 and 1.2 at an Mg#-value of 84.5-86.5. Clinopyroxene is low in Al2O3 with values 90% phlogopite. Perpotassic phlogopites with K/Al >1 values are typical for MARID-type xenoliths by comprising low Mg# of 82-88 (Dawson 1987). We performed thermobarometric calculations on the clinopyroxenes, by using the equations of Putirka (2008). With a proposed lamproitic melt, like Waters (1987) suggested for a MARID parental magma, a pressure of 13 kbar (39 km) and a temperature of 1300 C was calculated. This depth coincides with the crustal thickness of the Kaapvaal craton (Nguuri et al. 2001). However, the pressure calculations depend on the fractionation of Al between melt and mineral and are not realistic for low-Al diopsides. Calculations by Konzett et al. (2014) yielded 4.2 GPa (155 km) by using a Ca-in-opx thermometer and a cratonic geotherm of 40 mW/m² and seem to be more realistic. By applying a sandwich experimental approach, mixing glimmerite samples with harzburgitic peridotites, we hope to achieve deeper insights into the origin of MARID-type glimmerites

Flotation Behaviors of Perovskite, Titanaugite, and Magnesium Aluminate Spinel Using Octyl Hydroxamic Acid as the Collector

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Weiqing Wang

2017-08-01

Full Text Available The flotation behaviors of perovskite, titanaugite, and magnesium aluminate spinel (MA-spinel, using octyl hydroxamic acid (OHA as the collector, were investigated using microflotation experiments, zeta-potential measurements, Fourier transform infrared (FT-IR analyses, X-ray photoelectron spectroscopy (XPS analyses, and flotation experiments on artificially mixed minerals. The microflotation experiments show that the floatability of perovskite is clearly better than titanaugite and MA-spinel at around pH 5.5, while titanaugite possesses certain floatability at pH 6.0–6.5, and MA-spinel displays good floatability at pH > 8.0. The results of the FT-IR and XPS analyses show that OHA mainly interacts with Ti, resulting in perovskite flotation, and that the Al on titanaugite, as well as the Mg and Al on the MA-spinel surface, chemically react with OHA under acidic conditions. However, OHA mainly reacts with the Ti and Ca on the perovskite surface, Ca and Mg on the titanaugite surface, and Mg and Al on the MA-spinel surface under alkaline conditions. The results of the artificially mixed mineral flotation experiment show that the concentrate of TiO2 grade increased from 19.73% to 30.18% at pH 5.4, which indicates that a weakly acidic solution is the appropriate condition for the flotation separation of perovskite from titanaugite and MA-spinel. The results of the modified slag flotation experiments show that the TiO2 grade of concentrate increased from 18.13% to 23.88% at pH 5.4, through the open circuit test of “one roughing and one cleaning”. OHA displays selectivity toward perovskite in the modified slag flotation, but the consumption of H2SO4 is very high. The CaSO4 precipitate covered on the mineral surfaces results in poor TiO2 grade and recovery.

Olivine CPO in non-deformed peridotite due to topotactic replacement of antigorite

Science.gov (United States)

Nagaya, Takayoshi; Wallis, Simon; Kobayashi, Hiroaki; Michibayashi, Katsuyoshi; Mizukami, Tomoyuki; Seto, Yusuke; Miyake, Akira; Matsumoto, Megumi

2014-05-01

Olivine crystallographic preferred orientation (CPO) is thought to be the main cause of seismic anisotropy in the mantle, and its formation is generally considered to be the result of plastic deformation of mantle by dislocation creep. Olivine CPO has been reproduced in laboratory deformation experiments and considerable success has been achieved in understanding the deformation conditions (e.g. stress, temperature and water content) under which different olivine CPO patterns develop. This opens the possibility of mapping conditions in the mantle using seismic anisotropy and has been the subject of considerable study. Here we report an alternative mechanism for olivine CPO without the need for deformation. This process may be important in understanding the seismic properties of mantle in convergent margins. Metamorphic studies show peridotite in the Happo area, central Japan, formed by the dehydration of antigorite-schist related to contact metamorphism around a granite intrusion. Both field and microstructural observations suggest the olivine has not undergone strong plastic deformation. This was confirmed by TEM work that shows the olivine has very low dislocation densities and lacks low angle tilt boundaries. Such tilt boundaries are general stable even after annealing. These features show that peridotite in the Happo area formed in the absence of solid-state deformation. The olivine of the Happo peridotite formed dominantly by the dehydration breakdown of antigorite schist. We propose that the olivine CPO formed as a result of topotactic replacement of antigorite by the newly formed olivine. EBSD measurements in samples where both antigorite and new olivine are present and in contact show a very close crystallographic relationship between the two minerals: the a-axes are parallel, and the b- and c-axes are perpendicular. We conclude the strong olivine CPO in the Happo area was inherited from the original CPO of the antigorite. Such a process is likely to also

Mineral chemistry and geothemobarometry of mantle harzburgites in the Eastern Metamorphic Complex of Khoy ophiolite -NW Iran

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Morovvat Faridazad

2017-02-01

Full Text Available Introduction Khoy ophiolite at the global scale is in the middle part of the Alp-Himalaya orogenic belt and it is extended over 3900 Km2 which indicates remnant Neotethys oceanic lithosphere in the Mesozoic era (Kananian et al., 2010. In this paper, in addition to a review of previous investigations about Khoy ophiolite, we will try to determine the nature and kind of minerals, origin and partial melting rate as well as the equilibrium pressure and temperature of harzburgites from the Eastern Metamorphic Complex of Khoy ophiolite. Materials and methods Thin sections microscopy studies were carried out following field investigations. EPMA analysis was carried out with using a Superprobe JEOL, JXA 8200 Microprobe unit at the state of WDS and under condition of 15kv accelerating voltage, 10nA current beam, 1µm beam diameter and collection of natural and synthetic standards for calibration. Results The study area is located at the NW of Iran and north of the Khoy city in the west Azarbaijan province. This area is part of the ophiolitic complex of NW Iran and belongs to its Eastern Metamorphic Complex. This metamorphic zone has large tectonically segments of the metamorphic ophiolites which mainly include serpentinized peridotites with associated metagabbros. There are three types of peridotitic rocks in this area which are: Lherzolites, harzburgites and dunites. Lherzolites are composed of olivine (60-70%, orthopyroxene (10-30% and clinopyroxene (~10-20% with minor amounts (~2% of Cr-spinel mineral. Harzburgites are composed of olivine (70-80%, orthopyroxene (10-20% and clinopyroxene (~5% with minor amounts (~2% of Cr-spinel mineral. Dunites are composed of olivine (90-95%, orthopyroxene (5-10% with minor amounts (~1-2% of Cr-spinel mineral. Composition range of olivines is between Fo89.46 Fa10.37 to Fo89.86 Fa10.0 as well as NiO content range is 018-046 (wt %. The calculated Mg# of olivines is 0.90 and the composition of olivines in Fo-Fa diagram

Widespread melt/rock interaction and seismic properties of the lithosphere above mantle plumes: A petrological and microstructural study of mantle xenoliths from French Polynesia

Science.gov (United States)

Tommasi, A.; Godard, M.

2002-12-01

In addition to thermal erosion, plume/lithosphere interaction may induce significant changes in the lithosphere chemical composition. To constrain the extent of this process in an oceanic environment and its consequences on the lithosphere seismic properties, we studied the relationship between petrological processes and microstructure in mantle xenoliths from the Austral-Cook, Society and Marquesas islands. Olivine forsterite contents in our sp-peridotites vary continuously from Fo91 to Fo83, the lowest Fo being observed in dunites and wehrlites. Yet, their high Ni content (up to 2500 ppm) precludes a cumulate origin. These rocks are rather interpreted as resulting from melt/rock reactions involving olivine precipitation and pyroxene dissolution, the dunites indicating high melt-rock ratios. Moreover, wehrlites display poikiloblastic diopside enclosing corroded olivines. Late crystallization of clinopyroxene, also observed in lherzolites, may result from a near-solidus melt-freezing reaction occurring at the boundary of a partial melting domain developed at the expenses of lithospheric mantle. These data suggest that the lithosphere above a mantle plume undergoes a complex sequence of magmatic processes that significantly change its composition. Yet, crystal preferred orientations and thus seismic anisotropy are little affected by these processes. Lherzolites and harzburgites, independent from composition, show high-temperature porphyroclastic microstructures and strong olivine CPO. Although dunites and wehrlites display annealing microstructures to which is associated a progressive dispersion of the olivine CPO, very weak CPO are limited to a few dunites and wehrlites, suggesting that CPO destruction is restricted to domains of intense magma-rock interaction due to localized flow or accumulation of magmas. Conversely, the compositional changes result in lower seismic velocities for P- and S-waves. Relative to normal mantle, seismic anomalies may attain -2

A petrological view of early Earth geodynamics

Science.gov (United States)

Herzberg, C.

2003-04-01

Xenoliths of low T Archean cratonic mantle consist mostly of harzburgite and lherzolite with geochemical depletions that are characterisitc of igneous residues. Many authors have identified the complementary magmas as komatiites. This model is re-examined in light of work presented in Herzberg & O'Hara (2002) and found to be problematic. Munro-type alumina-undepleted komatiites from Alexo, Pyke Hill, and other locations often contain olivine phenocrysts with maximum Mg# \\cong 94. Residues of fractional melting would consist of pure dunite having Mg# = 97-98, but these are not observed. Residues of equilibrium melting would also be pure dunite with Mg# = 94, but these are also not observed. Olivines with Mg# = 94 are found in rare harzburgites, indicating that residues of alumina-undepleted komatiite have either been overprinted by subsequent magmatism or they have been geodynamically eroded. Alumina-undepleted komatiites can be successfully modeled with a primary magma containing 30% MgO produced by 0.5 mass fractions of equilibrium melting of depleted peridotite. A hot plume interpretation is consistent with both the petrology and helium isotopic compositions of alumina-undepleted komatiites. But what about cratonic mantle? The FeO and MgO contents of residues of fertile mantle peridotite formed by both equilibrium and fractional melting can be predicted and applied to xenoliths of cratonic mantle in most cases. Application to xenoliths from the Kaapvaal and Slave cratons is not possible owing to a second stage of Opx enrichment, but results can be applied to most xenoliths from Siberia, Tanzania, Somerset Island, and east Greenland as they contain less than 45% SiO_2. These xenoliths are very similar to residues produced by fractional melting. Pressures of initial melting were mostly 3 to 5 GPa, but can be as high 7 GPa. Pressures of final melting were highly variable and can be as low as 1 GPa. Potential temperatures (T_P) were typically 1450 to 1600oC and

Irradiation effects and behaviour of fission products in zirconia and spinel

International Nuclear Information System (INIS)

Gentils, A.

2003-10-01

Crystalline oxides, such as zirconia (ZrO 2 ) and spinel (MgAl 2 O 4 ), are promising inert matrices for the transmutation of plutonium and minor actinides. This work deals with the study of the physico-chemical properties of these matrices, more specifically their behaviour under irradiation and their capacity to retain fission products. Irradiations at low energy and incorporation of stable analogs of fission products (Cs, I, Xe) into yttria-stabilized zirconia and magnesium-aluminate spinel single crystals were performed by using the ion implanter IRMA (CSNSM-Orsay). Irradiations at high energy were made on several heavy ion accelerators (GANIL-Caen, ISL-Berlin, HIL-Warsaw). The damage induced by irradiation and the release of fission products were monitored by in situ Rutherford Backscattering Spectrometry experiments. Transmission electron microscopy was also used in order to determine the nature of the damage induced by irradiation. The results show that irradiation of ZrO 2 and MgAl 2 O 4 with heavy ions (about hundred keV and about hundred MeV) induces a huge structural damage in crystalline matrices. Total disorder (amorphization) is however never reached in zirconia, contrary to what is observed in the case of spinel. The results also emphasize the essential role played by the concentration of implanted species on their retention capacity. A dramatic release of fission products was observed when the concentration exceeds a threshold of a few atomic percent. Irradiation of implanted samples with medium-energy noble-gas ions leads to an enhancement of the fission product release. The exfoliation of spinel crystals implanted at high concentration of Cs ions is observed after a thermal treatment at high temperature. (author)

High-pressure behaviour of selenium-based spinels and related structures - an experimental and theoretical study

International Nuclear Information System (INIS)

Waskowska, A; Gerward, L; Olsen, J Staun; Feliz, M; Llusar, R; Gracia, L; Marques, M; Recio, J M

2004-01-01

The high-pressure structural behaviour of the cubic spinel CdCr 2 Se 4 (space group Fd3barm) and tetragonal CdGa 2 Se 4 (I4bar) has been investigated experimentally and theoretically in order to understand the large difference in compressibility between the two selenides. The experimental values of the bulk modulus for these compounds are 101(2) and 48(2) GPa, respectively. These values compare well with 92 and 44 GPa obtained from first-principles calculations based on the density functional theory formalism. The observed difference in compressibility between the cubic and tetragonal structures can be understood in terms of polyhedral analysis. In a hypothetical cubic spinel structure Fd3barm), the calculated bulk modulus for CdGa 2 Se 4 is 85 GPa. This value together with the experimental and theoretical results for CdCr 2 Se 4 suggest that the selenium-based cubic spinels should have a bulk modulus about 100 GPa, which is half the value found for the oxide spinels

Direct observation of cation distributions of ideal inverse spinel CoFe2O4 nanofibres and correlated magnetic properties

KAUST Repository

Zeng, Xue

2017-04-25

Low-dimensional spinel ferrites have recently attracted increasing attention because their tunable magnetic properties make them attractive candidates as spin-filtering tunnel barriers in spintronic devices and as magnetic components in artificial multiferroic heterostructures. Although we know that the distribution of cations (Fe3+ and Co2+) in a spinel structure governs its magnetic properties, their distribution in the so-called ideal inverse spinel structure of a ferrite, CoFe2O4, has not yet been imaged with sub-ångstrom resolution. In this work, we fill this gap in evidence by reporting a direct observation of the distribution of cations in an ideal inverse spinel structure of CoFe2O4 nanofibres using aberration-corrected transmission electron microscopy (TEM). The ordering of Co2+ and Fe3+ at the octahedral sites imaged along either [001], [011] or [-112] orientation was identified as 1 : 1, in accordance with the ideal inverse spinel structure. The saturation magnetisation calculated based on the crystal structure as determined from the TEM image is in good agreement with that measured experimentally on the spinel CoFe2O4 nanofibres, further confirming results from TEM.

The petrology, geochronology and significance of Granite Harbour Intrusive Complex xenoliths and outcrop sampled in western McMurdo Sound, Southern Victoria Land, Antarctica

International Nuclear Information System (INIS)

Martin, A.P.; Cooper, A.F.; Price, R.C.; Turnbull, R.E.; Roberts, N.M.W.

2015-01-01

Granite Harbour Intrusive Complex xenoliths in McMurdo Volcanic Group rocks and in situ outcrops have been studied from Mount Morning, western McMurdo Sound, Antarctica. Calc-alkalic samples have whole rock signatures and normative compositions similar to the Dry Valleys 1b suite, and zircon grains in one specimen yield a 545.2 ± 4.4 Ma crystallisation age. This supports subduction-related magmatism initiating in Southern Victoria Land by 545 Ma. A second group of xenoliths is alkalic, with titanite grains in one xenolith from this group dated at 538 ± 8 Ma. Whole rock chemistry, normative compositions and geochronology of the alkalic group are comparable to the Koettlitz Glacier Alkaline Suite (KGAS). The position of a proposed lower crustal discontinuity that may form a significant basement suture in the McMurdo Sound region is newly constrained to the east of Mount Morning, perhaps along the trace of the Discovery Glacier. The boundary between East and West Antarctica may also pass along the trace of the Discovery Glacier if, as previously hypothesised, its location is controlled by the basement suture. A significant basement suture may also have provided the necessary egress for the (regionally) early and sustained magmatic activity observed at Mount Morning over the last 24 million years. (author).

Microfracturing and fluid pathways in serpentinizing abyssal peridotites along the Southwest Indian Ridge (62°-65°E)

Science.gov (United States)

Rouméjon, S.; Cannat, M.; Agrinier, P.; Godard, M.; Andreani, M.

2013-12-01

At slow spreading ridges, axial detachment faults exhume mantle-derived peridotites. Their interaction with seawater-derived hydrothermal fluids causes serpentinization down to 2-3km from the fault, as inferred from seismic velocity models. It is commonly proposed that fractures allow penetration of seawater into the fault's footwall. At the microscopic scale, the hydration front progresses from a microfracture network toward the center of olivine relicts and forms the serpentine mesh texture. The origin of these microfractures is a matter of debate: tectonic, anisotropic thermal contraction of olivine during peridotite cooling or hierarchical fracturing of the olivine due to volume increase during serpentinization. In this presentation we use petrology and geochemistry to analyze the links between microfractures and serpentinization in a set of highly serpentinized peridotites dredged along the melt-starved easternmost part of the Southwest Indian Ridge (Smoothseafloor cruise). Our observations suggest that thermal contraction of olivine combines with tectonic stresses to fracture fresh peridotite in the brittle lithosphere. These ~60μm-spaced microfractures constitute the initial sample-scale permeability network for fluid penetration, onset of serpentinization and formation of additional hierarchical fractures. As serpentinization proceeds, the volume increase closes the least-developed planes and preferential pathways for fluid circulation become more distant, forming the 200-500μm-wide polygonal pattern typical of the serpentine mesh texture. In about 20% of the recovered samples the mesh serpentine is partially recrystallized forming rims next to later microfractures and serpentine veins. The spacing of these rims, and the limited proportion of affected samples suggest that the scales of the efficient permeability network in the serpentinites at this stage had increased to decimetric and greater scales. We use geochemical constrains to derive temperature

Origin and Distribution of Water Contents in Continental and Oceanic Lithospheric Mantle

Science.gov (United States)

Peslier, Anne H.

2013-01-01

The water content distribution of the upper mantle will be reviewed as based on the peridotite record. The amount of water in cratonic xenoliths appears controlled by metasomatism while that of the oceanic mantle retains in part the signature of melting events. In both cases, the water distribution is heterogeneous both with depth and laterally, depending on localized water re-enrichments next to melt/fluid channels. The consequence of the water distribution on the rheology of the upper mantle and the location of the lithosphere-asthenosphere boundary will also be discussed.

Seismic anisotropies of the Songshugou peridotites (Qinling orogen, central China) and their seismic implications

Science.gov (United States)

Cao, Yi; Jung, Haemyeong; Song, Shuguang

2018-01-01

Though extensively studied, the roles of olivine crystal preferred orientations (CPOs or fabrics) in affecting the seismic anisotropies in the Earth's upper mantle are rather complicated and still not fully known. In this study, we attempted to address this issue by analyzing the seismic anisotropies [e.g., P-wave anisotropy (AVp), S-wave polarization anisotropy (AVs), radial anisotropy (ξ), and Rayleigh wave anisotropy (G)] of the Songshugou peridotites (dunite dominated) in the Qinling orogen in central China, based on our previously reported olivine CPOs. The seismic anisotropy patterns of olivine aggregates in our studied samples are well consistent with the prediction for their olivine CPO types; and the magnitude of seismic anisotropies shows a striking positive correlation with equilibrium pressure and temperature (P-T) conditions. Significant reductions of seismic anisotropies (AVp, max. AVs, and G) are observed in porphyroclastic dunite compared to coarse- and fine-grained dunites, as the results of olivine CPO transition (from A-/D-type in coarse-grained dunite, through AG-type-like in porphyroclastic dunite, to B-type-like in fine-grained dunite) and strength variation (weakening: A-/D-type → AG-type-like; strengthening: AG-type-like → B-type-like) during dynamic recrystallization. The transition of olivine CPOs from A-/D-type to B-/AG-type-like in the forearc mantle may weaken the seismic anisotropies and deviate the fast velocity direction and the fast S-wave polarization direction from trench-perpendicular to trench-oblique direction with the cooling and aging of forearc mantle. Depending on the size and distribution of the peridotite body such as the Songshugou peridotites, B- and AG-type-like olivine CPOs can be an additional (despite minor) local contributor to the orogen-parallel fast velocity direction and fast shear-wave polarization direction in the orogenic crust such as in the Songshugou area in Qinling orogen.

The centralized control of elemental mercury emission from the flue gas by a magnetic rengenerable Fe-Ti-Mn spinel.

Science.gov (United States)

Liao, Yong; Xiong, Shangchao; Dang, Hao; Xiao, Xin; Yang, Shijian; Wong, Po Keung

2015-12-15

A magnetic Fe-Ti-Mn spinel was developed to adsorb gaseous Hg(0) in our previous study. However, it is currently extremely restricted in the control of Hg(0) emission from the flue gas for at least three reasons: sorbent recovery, sorbent regeneration and the interference of the chemical composition in the flue gas. Therefore, the effect of SO2 and H2O on the adsorption of gaseous Hg(0) on the Fe-Ti-Mn spinel and the regeneration of spent Fe-Ti-Mn spinel were investigated in this study. Meanwhile, the procedure of the centralized control of Hg(0) emission from the flue gas by the magnetic Fe-Ti-Mn spinel has been analyzed for industrial application. The spent Fe-Ti-Mn spinel can be regenerated by water washing followed by the thermal treatment at 450 °C with no obvious decrease of its ability for Hg(0) capture. Meanwhile, gaseous Hg(0) in the flue gas can be remarkably concentrated during the regeneration, facilitating its safe disposal. Initial pilot test demonstrated that gaseous Hg(0) in the real flue gas can be concentrated at least 100 times by the Fe-Ti-Mn spinel. Therefore, Fe-Ti-Mn spinel was a novel magnetic regenerable sorbent, which can be used for the centralized control of Hg(0) emission from the flue gas. Copyright © 2015 Elsevier B.V. All rights reserved.

Effects of synthetic parameters on structure and electrochemical performance of spinel lithium manganese oxide by citric acid-assisted sol-gel method

International Nuclear Information System (INIS)

Yi Tingfeng; Dai Changsong; Gao Kun; Hu Xinguo

2006-01-01

The spinel lithium manganese oxide cathode materials were prepared by citric acid-assisted sol-gel method at 623-1073 K in air. The effects of pH value, raw material, synthesis temperature and time on structure and electrochemical performance of spinel lithium manganese oxide are investigated by X-ray diffraction (XRD), scanning electronic microscope (SEM) and cyclic voltammetry (CV). XRD data results strongly suggest that the synthesis temperature is the dominating factors of the formation of spinel phase, and spinel lithium manganese oxide powder with various crystallites size can be obtained by controlling the sintering time. CV shows that spinel lithium manganese oxide powder formed about 973 K presents the best electrochemical performance with well separated two peaks and the highest peak current. Charge-discharge test indicates that spinel lithium manganese oxide powders calcined at higher temperatures have high discharge capacity and capacity loss, and sintered at lower temperatures has low discharge capacity and high capacity retention

Effects of synthetic parameters on structure and electrochemical performance of spinel lithium manganese oxide by citric acid-assisted sol-gel method

Energy Technology Data Exchange (ETDEWEB)

Yi Tingfeng [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China)]. E-mail: tfyihit@hit.edu.cn; Dai Changsong [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China); Gao Kun [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China); Hu Xinguo [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China)

2006-11-30

The spinel lithium manganese oxide cathode materials were prepared by citric acid-assisted sol-gel method at 623-1073 K in air. The effects of pH value, raw material, synthesis temperature and time on structure and electrochemical performance of spinel lithium manganese oxide are investigated by X-ray diffraction (XRD), scanning electronic microscope (SEM) and cyclic voltammetry (CV). XRD data results strongly suggest that the synthesis temperature is the dominating factors of the formation of spinel phase, and spinel lithium manganese oxide powder with various crystallites size can be obtained by controlling the sintering time. CV shows that spinel lithium manganese oxide powder formed about 973 K presents the best electrochemical performance with well separated two peaks and the highest peak current. Charge-discharge test indicates that spinel lithium manganese oxide powders calcined at higher temperatures have high discharge capacity and capacity loss, and sintered at lower temperatures has low discharge capacity and high capacity retention.

Stretched-to-compressed-exponential crossover observed in the electrical degradation kinetics of some spinel-metallic screen-printed structures

Science.gov (United States)

Balitska, V.; Shpotyuk, O.; Brunner, M.; Hadzaman, I.

2018-02-01

Thermally-induced (170 °C) degradation-relaxation kinetics is examined in screen-printed structures composed of spinel Cu0.1Ni0.1Co1.6Mn1.2O4 ceramics with conductive Ag or Ag-Pd layered electrodes. Structural inhomogeneities due to Ag and Ag-Pd diffusants in spinel phase environment play a decisive role in non-exponential kinetics of negative relative resistance drift. If Ag migration in spinel is inhibited by Pd addition due to Ag-Pd alloy, the kinetics attains stretched exponential behavior with ∼0.58 exponent, typical for one-stage diffusion in structurally-dispersive media. Under deep Ag penetration into spinel ceramics, as for thick films with Ag-layered electrodes, the degradation kinetics drastically changes, attaining features of two-step diffusing process governed by compressed-exponential dependence with power index of ∼1.68. Crossover from stretched- to compressed-exponential kinetics in spinel-metallic structures is mapped on free energy landscape of non-barrier multi-well system under strong perturbation from equilibrium, showing transition with a character downhill scenario resulting in faster than exponential decaying.

The effect of Y2O3 addition on thermal shock behavior of magnesium aluminate spinel

Directory of Open Access Journals (Sweden)

Pošarac Milica

2009-01-01

Full Text Available The effect of yttria additive on the thermal shock behavior of magnesium aluminate spinel has been investigated. As a starting material we used spinel (MgAl2O4 obtained by the modified glycine nitrate procedure (MGNP. Sintered products were characterized in terms of phase analysis, densities, thermal shock, monitoring the damaged surface area in the refractory specimen during thermal shock and ultrasonic determination of the Dynamic Young modulus of elasticity. It was found that a new phase between yttria and alumina is formed, which improved thermal shock properties of the spinel refractories. Also densification of samples is enhanced by yttria addition.

Manufacturing process scale-up of optical grade transparent spinel ceramic at ArmorLine Corporation

Science.gov (United States)

Spilman, Joseph; Voyles, John; Nick, Joseph; Shaffer, Lawrence

2013-06-01

While transparent Spinel ceramic's mechanical and optical characteristics are ideal for many Ultraviolet (UV), visible, Short-Wave Infrared (SWIR), Mid-Wave Infrared (MWIR), and multispectral sensor window applications, commercial adoption of the material has been hampered because the material has historically been available in relatively small sizes (one square foot per window or less), low volumes, unreliable supply, and with unreliable quality. Recent efforts, most notably by Technology Assessment and Transfer (TA and T), have scaled-up manufacturing processes and demonstrated the capability to produce larger windows on the order of two square feet, but with limited output not suitable for production type programs. ArmorLine Corporation licensed the hot-pressed Spinel manufacturing know-how of TA and T in 2009 with the goal of building the world's first dedicated full-scale Spinel production facility, enabling the supply of a reliable and sufficient volume of large Transparent Armor and Optical Grade Spinel plates. With over $20 million of private investment by J.F. Lehman and Company, ArmorLine has installed and commissioned the largest vacuum hot press in the world, the largest high-temperature/high-pressure hot isostatic press in the world, and supporting manufacturing processes within 75,000 square feet of manufacturing space. ArmorLine's equipment is capable of producing window blanks as large as 50" x 30" and the facility is capable of producing substantial volumes of material with its Lean configuration and 24/7 operation. Initial production capability was achieved in 2012. ArmorLine will discuss the challenges that were encountered during scale-up of the manufacturing processes, ArmorLine Optical Grade Spinel optical performance, and provide an overview of the facility and its capabilities.

Effect of Feed Melting, Temperature History and Minor Component Addition on Spinel Crystallization in High-Level Waste Glass

International Nuclear Information System (INIS)

Izak, Pavel; Hrma, Pavel R.; Arey, Bruce W.; Plaisted, Trevor J.

2001-01-01

This study was undertaken to help design mathematical models for high-level waste (HLW) glass melter that simulate spinel behavior in molten glass. Spinel, (Fe,Ni,Mn) (Fe,Cr)2O4, is the primary solid phase that precipitates from HLW glasses containing Fe and Ni in sufficient concentrations. Spinel crystallization affects the anticipated cost and risk of HLW vitrification. To study melting reactions, we used simulated HLW feed, prepared with co-precipitated Fe, Ni, Cr, and Mn hydroxides. Feed samples were heated up at a temperature-increase rate (4C/min) close to that which the feed experiences in the HLW glass melter. The decomposition, melting, and dissolution of feed components (such as nitrates, carbonates, and silica) and the formation of intermediate crystalline phases (spinel, sodalite (Na8(AlSiO4)6(NO2)2), and Zr-containing minerals) were characterized using evolved gas analysis, volume-expansion measurement, optical microscope, scanning electron microscope, thermogravimetric analysis, differential scanning calorimetry, and X-ray diffraction. Nitrates and quartz, the major feed components, converted to a glass-forming melt by 880C. A chromium-free spinel formed in the nitrate melt starting from 520C and Sodalite, a transient product of corundum dissolution, appeared above 600C and eventually dissolved in glass. To investigate the effects of temperature history and minor components (Ru,Ag, and Cu) on the dissolution and growth of spinel crystals, samples were heated up to temperatures above liquidus temperature (TL), then subjected to different temperature histories, and analyzed. The results show that spinel mass fraction, crystals composition, and crystal size depend on the chemical and physical makeup of the feed and temperature history

Spinel Li2CoTi3O8 nanometer obtained for application as pigment

International Nuclear Information System (INIS)

Costa de Camara, M. S.; Alves Pimentel, L.; Longo, E.; Nobrega Azevedo, L. da; Araujo Melo, D. M. de

2016-01-01

Pigments are used in ceramics, cosmetics, inks, and other applications widely materials. To this must be single and easily reproducible. Moreover, the pigments obtained in the nanoscale are more stable, reproducible and highlight color in small amounts compared with those obtained in micrometer scale. The mixed oxides with spinel structures AB 2 O 4 have important applications, including: pigments, refractories, catalytic and electronic ceramics. In this context, the aim of this work was the preparation of powder Li 2 CoTi 3 O 8 spinel phase with nanometer particle size of the polymeric precursor method (Pechini) and characterization by means of thermal analysis (TG/DTA) X-ray diffraction (XRD), refined by the Rietveld method, BET, transmission electron microscopy (TEM), Raman and colorimetric coordinates. The pigment was obtained by heat treatment of 400 degree centigrade to 1000 degree centigrade after pyrolysis at 300 degree centigrade/1 h for removing the organic material. Li 2 CoTi 3 O 8 desired spinel phase was obtained from 500 degree centigrade, and presenting stability nanometer to about 1.300 degree centigrade. Spinel green phase introduced at temperatures in the range of 400 degree centigrade and 500 degree centigrade, and 600 degree centigrade at temperatures between blue and 1000 degree centigrade. (Author)

Lattice parameters and stability of the spinel compounds in relation to the ionic radii and electronegativities of constituting chemical elements.

Science.gov (United States)

Brik, Mikhail G; Suchocki, Andrzej; Kamińska, Agata

2014-05-19

A thorough consideration of the relation between the lattice parameters of 185 binary and ternary spinel compounds, on one side, and ionic radii and electronegativities of the constituting ions, on the other side, allowed for establishing a simple empirical model and finding its linear equation, which links together the above-mentioned quantities. The derived equation gives good agreement between the experimental and modeled values of the lattice parameters in the considered group of spinels, with an average relative error of about 1% only. The proposed model was improved further by separate consideration of several groups of spinels, depending on the nature of the anion (oxygen, sulfur, selenium/tellurium, nitrogen). The developed approach can be efficiently used for prediction of lattice constants for new isostructural materials. In particular, the lattice constants of new hypothetic spinels ZnRE2O4, CdRE2S4, CdRE2Se4 (RE = rare earth elements) are predicted in the present Article. In addition, the upper and lower limits for the variation of the ionic radii, electronegativities, and their certain combinations were established, which can be considered as stability criteria for the spinel compounds. The findings of the present Article offer a systematic overview of the structural properties of spinels and can serve as helpful guides for synthesis of new spinel compounds.

Spinel dissolution via addition of glass forming chemicals. Results of preliminary experiments

Energy Technology Data Exchange (ETDEWEB)

Fox, K. M. [Savannah River Site (SRS), Aiken, SC (United States); Johnson, F. C. [Savannah River Site (SRS), Aiken, SC (United States)

2015-11-01

Increased loading of high level waste in glass can lead to crystallization within the glass. Some crystalline species, such as spinel, have no practical impact on the chemical durability of the glass, and therefore may be acceptable from both a processing and a product performance standpoint. In order to operate a melter with a controlled amount of crystallization, options must be developed for remediating an unacceptable accumulation of crystals. This report describes preliminary experiments designed to evaluate the ability to dissolve spinel crystals in simulated waste glass melts via the addition of glass forming chemicals (GFCs).

Modification of Alumina and Spinel Inclusions by Calcium in Liquid Steel

Science.gov (United States)

Verma, Neerav

2011-12-01

Steel Cleanliness plays a crucial role in determining steel properties such as toughness, ductility, formability, corrosion resistance and surface quality. The production of clean steel often involves the elimination or chemical and morphological modification of oxide and sulfide inclusions. Along with deteriorating the steel properties, solid inclusions can affect steel castability through nozzle clogging. Nozzle clogging occurs when solid inclusions accumulate in the caster pouring system such as the ladle shroud or submerged entry nozzle (SEN). Thus, it is important to understand how to achieve desired inclusion characteristics (shape, size and chemistry) through the steelmaking process. Among the various practices adopted in industries to counteract the effect of solid inclusions, modification of solid inclusions to liquid or partially liquid state through calcium treatment is one of the methods. Calcium can be used because it has a strong ability to form oxides and sulfides. In Al-killed steels, the most common inclusions are alumina (Al2O3) inclusions, which are solid at steelmaking temperatures. On calcium treatment, solid alumina inclusions are converted to calcium aluminates, which have liquidus temperatures lower than steelmaking temperature (1600°C) [14]. It has been found that alumina inclusions may contain some MgO and such inclusions are termed alumina magnesia spinels (Al2O3.xMgO) [18]. These spinels are more stable than alumina and it has been suggested that they might be more difficult to modify [18]. But, some authors have proposed that MgO can actually help in the liquefaction of inclusions, and have demonstrated successful modification of spinels by Ca treatment [20, 21]. In the present research, the mechanism of transformation of alumina and spinel inclusions upon calcium treatment was studied by characterizing transient evolution of inclusions. A vacuum induction was used for melting, making additions (Al, Al-Mg and CaSi2) and sampling. The

Corundum-to-spinel structural phase transformation in alumina

Energy Technology Data Exchange (ETDEWEB)

Adachi, Shogo [Department of Materials Science and Engineering, Kyushu Institute of Technology, Fukuoka 804-8550 (Japan); Ishimaru, Manabu, E-mail: ishimaru@post.matsc.kyutech.ac.jp [Department of Materials Science and Engineering, Kyushu Institute of Technology, Fukuoka 804-8550 (Japan); Sina, Younes; McHargue, Carl J.; Sickafus, Kurt E. [Materials Science and Engineering Department, University of Tennessee, Knoxville, TN 37996-2200 (United States); Alves, Eduardo [Unit of Physics and Accelerators, Ion Beam Laboratory, Instituto Superior Técnico/Instituto Tecnológico e Nuclear, EN. 10 2686-953 Sacavém (Portugal)

2015-09-01

Several polymorphs exist in alumina (Al{sub 2}O{sub 3}), and they transform to a stable α-phase with a hexagonal corundum structure on thermal annealing. This structural change is irreversible as a function of temperature, and transformation of corundum to another metastable crystalline phase has never been observed by heat treatments. In this study, we irradiated single crystals of Al{sub 2}O{sub 3} with Zr ions and obtained an irradiated microstructure consisting of a buried α-Al{sub 2}O{sub 3} layer surrounded on top and bottom by layers of a defect cubic spinel Al{sub 2}O{sub 3} phase. We examined the thermal stability of this microstructure using transmission electron microscopy and X-ray diffraction. We found that the corundum phase completely transforms to the spinel phase following annealing at 1173 K for 1 h: the thermodynamically stable phase transforms to the metastable phase by heat treatments. We discuss this unusual structural change within the context of our results as well as previous observations.

Coincident site lattice-matched InGaN on (111) spinel substrates

International Nuclear Information System (INIS)

Norman, A. G.; Dippo, P. C.; Moutinho, H. R.; Simon, J.; Ptak, A. J.

2012-01-01

Coincident site lattice-matched wurtzite (0001) In 0.31 Ga 0.69 N, emitting in the important green wavelength region, is demonstrated by molecular beam epitaxy on a cubic (111) MgAl 2 O 4 spinel substrate. The coincident site lattice matching condition involves a 30 deg. rotation between the lattice of the InGaN epitaxial layer and the lattice of the spinel. This work describes an alternative approach towards realizing more compositionally homogenous InGaN films with low dislocation density emitting in the ''green gap'' of low efficiency currently observed for semiconductor light emitting diodes (LEDs). This approach could lead to higher efficiency green LEDs presently of great interest for solid-state lighting applications.

The ongoing search for the oldest rock on the Danish island of Bornholm: new U-Pb zircon ages for a quartz-rich xenolith and country rock from the Svaneke Granite

DEFF Research Database (Denmark)

Waight, Tod Earle; Serre, Simon H.; Næsby, Sebastian H.

2017-01-01

Previous geochronological studies on the Danish island of Bornholm have not identified any rocks older than c. 1.46 Ga. New LA-ICP-MS U-Pb zircon ages are presented for a xenolith within, and the country rock gneiss adjacent to, the Svaneke Granite on Bornholm. The xenolith is fine......-grained and quartz-rich and was likely derived from either a quartz-rich sedimentary protolith or a hydrothermally altered felsic volcanic rock. The relatively fine-grained felsic nature of the country rock gneiss and the presence of large zoned feldspars that may represent phenocrysts suggest its protolith may have...... been a felsic volcanic or shallow intrusive rock. A skarn-like inclusion from a nearby locality likely represents an originally carbonate sediment and is consistent with supracrustal rocks being present at least locally. Zircon data from the xenolith define an upper intercept age of 1483 ± 12 Ma (2σ...

A series of spinel phase cathode materials prepared by a simple hydrothermal process for rechargeable lithium batteries

International Nuclear Information System (INIS)

Liang Yanyu; Bao Shujuan; Li Hulin

2006-01-01

A series of spinel-structured materials have been prepared by a simple hydrothermal procedure in an aqueous medium. The new synthetic method is time and energy saving i.e., no further thermal treatment and extended grinding. The main experimental process involved the insertion of lithium into electrolytic manganese dioxide with glucose as a mild reductant in an autoclave. Both the hydrothermal temperature and the presence of glucose play the critical roles in determining the final spinel integrity. Particular electrochemical performance has also been systematically explored, and the results show that Al 3+ , F - co-substituted spinels have the best combination of initial capacity and capacity retention among all these samples, exhibited the initial capacity of 115 mAh/g and maintained more than 90% of the initial value at the 50th cycle. - Graphical abstract: It is a SEM image of the spinel LiMn 2 O 4 , which was prepared by this novel hydrothermal procedure. It illustrates that reasonable-crystallized spinel oxide has occurred through the special hydrothermal process and the average particle size declined to about 1 μm. This homogeneous grain size distribution provides an important morphological basis for the reversibility and accessibility of lithium ion insertion/extraction reactions

Phase control of Mn-based spinel films via pulsed laser deposition

International Nuclear Information System (INIS)

Feng, Zhenxing; Chen, Xiao; Fister, Timothy T.; Bedzyk, Michael J.; Fenter, Paul

2016-01-01

Phase transformations in battery cathode materials during electrochemical-insertion reactions lead to capacity fading and low cycle life. One solution is to keep the same phase of cathode materials during cation insertion-extraction processes. Here, we demonstrate a novel strategy to control the phase and composition of Mn-based spinel oxides for magnesium-ion battery applications through the growth of thin films on lattice-matched substrates using pulsed laser deposition. Materials at two extreme conditions are considered: fully discharged cathode MgMn_2O_4 and fully charged cathode Mn_2O_4. The tetragonal MgMn_2O_4 (MMO) phase is obtained on MgAl_2O_4 substrates, while the cubic MMO phase is obtained on MgO substrates. Similarly, growth of the empty Mn_2O_4 spinel in the cubic phase is obtained on an MgO substrate. These results demonstrate the ability to control separately the phase of spinel thin films (e.g., tetragonal vs. cubic MMO) at nominally fixed composition, and to maintain a fixed (cubic) phase while varying its composition (MgxMn_2O_4, for x = 0, 1). As a result, this capability provides a novel route to gain insights into the operation of battery electrodes for energy storage applications.

NiO and Fe/Mn in Fo-rich olivines from OIB, MORB, and mantle peridotites

Science.gov (United States)

Li, H.; Baker, M.; Hofmann, A. E.; Clague, D.; Stolper, E.

2006-12-01

Olivines from mantle peridotites have a narrow range of NiO (0.36±0.03 [1σ] wt%), but NiO of olivines in basalts suggest NiO in mantle olivines is actually more variable: e.g., Hawaiian phenocrysts (Fo>90) have NiO >0.55%, and olivines from continental flood basalts can have >0.5% NiO. At the other end of the spectrum, some basaltic suites (e.g., Iceland, MORBs) have Fo>90 olivines with NiO >0.2%. Partial melting calculations on peridotites show it is difficult to generate liquids that crystallize Fo>90 olivines with >0.4% NiO without resorting to complex processes. Hypotheses to explain the variability of NiO in mantle-derived olivines include (1) reaction of peridotite with silica-rich melts of eclogite results in decreasing modal abundance of olivine and increasing NiO in olivine [1,2]; (2) magmas with NiO-rich olivines come from sources enriched in NiO due to a core-derived component [3]. [4] proposed that high Fe/Mn of Hawaiian vs. Icelandic and MORB lavas reflect a core-derived component in their sources. Possible core incorporation is poorly constrained but FeO and NiO are expected to increase by such processes, leading to correlations between NiO and Fe/Mn in mantle rocks with significant core-derived components. We present high-precision analyses of Fo-rich olivines from OIBs, MORBs, komatiites, and mantle peridotites, focusing on NiO contents and Fe/Mn ratios. Our goal is to test hypotheses to explain elevated NiO of Fo-rich olivines in basalts. Olivines are Fo85.1-93.4; more were analyzed, but we focused on this range to avoid complications due to decreasing NiO in olivine with crystallization. Errors (1σ) are 0.01 wt% in NiO and 1.5 in Fe/Mn (wt). Our data show several features: (1) NiO contents and Fe/Mn ratios of Fo>88 olivines are positively correlated, with the low end of the trend (NiO ~0.23%, Fe/Mn ~61) defined by MORB and Iceland and the high end of the trend (NiO ~0.55%, Fe/Mn ~80) by Reunion and Hawaii. Between these end points, there is a

Nanocrystalline spinel ferrites by solid state reaction route

Indian Academy of Sciences (India)

Wintec

Nanocrystalline spinel ferrites by solid state reaction route. T K KUNDU* and S MISHRA. Department of Physics, Visva-Bharati, Santiniketan 731 235, India. Abstract. Nanostructured NiFe2O4, MnFe2O4 and (NiZn)Fe2O4 were synthesized by aliovalent ion doping using conventional solid-state reaction route. With the ...

Synthesis and magnetic properties of Zn Spinel ceramics

Czech Academy of Sciences Publication Activity Database

Huber, Š.; Sofer, Z.; Nádherný, L.; Jankovský, O.; Šimek, P.; Sedmidubský, D.; Maryško, Miroslav

2013-01-01

Roč. 57, č. 2 (2013), s. 162-166 ISSN 0862-5468 R&D Projects: GA ČR GA13-17538S; GA MŠk(CZ) 7AMB12FR019 Institutional support: RVO:68378271 Keywords : Zn spinel * synthesis * magnetic properties * antiferromagnet * bulk ZnO Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 0.434, year: 2013

Metasomatic Reaction Zones as Monitors of Trace Element Transfer at the Slab-Mantle Interface: the Case of the Hochwart Peridotite (Ulten Zone, Italy)

Science.gov (United States)

Marocchi, M.; Hermann, J.; Bargossi, G. M.; Mair, V.; Morten, L.

2006-12-01

Ultramafic blocks belonging to the Hochwart peridotite outcrop (Ulten Zone, Italian Alps) preserve a series of metasomatic mineral zones generated by infiltration of Si-rich hydrous fluids which occurred at the gneiss- peridotite interface. The age of the high pressure metamorphism for the Hochwart complex has been constrained at 330 Ma (Tumiati et al., 2003, EPSL, 210, 509-526). The country rocks are stromatic gneisses consisting mainly of quartz, K-feldspar, garnet, kyanite, biotite and muscovite. The ultramafic body consists of strongly serpentinized metaperidotites which are exposed as a hectometre-size lens along a steep gully, associated to monomineralic zones that developed at the contact between the peridotite body and the garnet gneiss country rocks. The composition of the metasomatic zones has been investigated in detail and records an order of metasomatic zoning formed by phlogopite-rich to tremolite-anthophyllite-rich rocks going from the host gneiss towards the peridotite. In some cases, the ultramafics fade into the gneisses developing serpentine and talc which has replaced, presumably at lower temperatures, the serpentine matrix and occurs in association with chlorite. Phlogopite aggregates (phlogopitite) with accessory minerals (quartz + zircon + apatite) and metabasic pods (phlogopite and hornblende) also occur. Black tourmaline (schorl-dravite solid solution) has been found for the first time in the contact near the phlogopite zone, suggesting an external addition of elements (boron and fluorine) to the system at high temperature. The formation of the metasomatic zones composed exclusively of hydrous phases must have involved extensive H2O-metasomatism as already documented for the Ulten peridotites. The source for these fluids can be a system of trondhjemitic-pegmatitic dikes cutting the peridotite that would have channelled aqueous fluids into the ultramafic rocks. Whole-rock geochemistry and trace element (LA ICP-MS) composition of hydrous

Li Isotope Studies of Olivine in Mantle Xenoliths by SIMS

Science.gov (United States)

Bell, D. R.; Hervig, R. L.; Buseck, P. R.

2005-01-01

Variations in the ratio of the stable isotopes of Li are a potentially powerful tracer of processes in planetary and nebular environments [1]. Large differences in the 7Li/6Li ratio between the terrestrial upper mantle and various crustal materials make Li isotope composition a potentially powerful tracer of crustal recycling processes on Earth [2]. Recent SIMS studies of terrestrial mantle and Martian meteorite samples report intra-mineral Li isotope zoning [3-5]. Substantial Li isotope heterogeneity also exists within and between the components of chondritic meteorites [6,7]. Experimental studies of Li diffusion suggest the potential for rapid isotope exchange at elevated temperatures [8]. Large variations in 7Li, exceeding the range of unaltered basalts, occur in terrestrial mantle-derived xenoliths from individual localities [9]. The origins of these variations are not fully understood.

Coincident site lattice-matched InGaN on (111) spinel substrates

Energy Technology Data Exchange (ETDEWEB)

Norman, A. G.; Dippo, P. C.; Moutinho, H. R.; Simon, J.; Ptak, A. J. [National Renewable Energy Laboratory, Golden, Colorado 80401 (United States)

2012-04-09

Coincident site lattice-matched wurtzite (0001) In{sub 0.31}Ga{sub 0.69}N, emitting in the important green wavelength region, is demonstrated by molecular beam epitaxy on a cubic (111) MgAl{sub 2}O{sub 4} spinel substrate. The coincident site lattice matching condition involves a 30 deg. rotation between the lattice of the InGaN epitaxial layer and the lattice of the spinel. This work describes an alternative approach towards realizing more compositionally homogenous InGaN films with low dislocation density emitting in the ''green gap'' of low efficiency currently observed for semiconductor light emitting diodes (LEDs). This approach could lead to higher efficiency green LEDs presently of great interest for solid-state lighting applications.

Volatile-rich komatiitic and picritic melt inclusions in Cr-spinel beach sand from Gorgona Island, Colombia

Science.gov (United States)

Shimizu, K.; Shimizu, N.; Suzuki, K.; Tatsumi, Y.; Komiya, T.; Maruyama, S.

2007-12-01

Volatile content of komatiite is a key to constrain thermal evolution of the deep Earth. We report volatile contents with major and trace element compositions of melt inclusions (MIs) in chromian spinel (Cr-spinel) from beach sands of Gorgona Island, Colombia. Gorgona Island is ~90 Ma volcanic island, where picrites and the world-youngest komatiites occur. As Cr-spinel is dense and rigid oxide mineral that crystallizes only at early stages of crystallization, it is considered to be a superior container for retaining primitive melt, even including volatiles. Volatile (H2O, CO2, S, F and Cl) and trace element (K2O, Sr, Y, Zr, Nb, Ba, La, Ce, Sm, Dy, Yb) compositions of ~80 MIs were analyzed by SIMS (Cameca-1280 and 3f, respectively) at WHOI. MIs in the Cr-spinel from Gorgona Is. are classified into three types by their host Cr-spinel compositions such as low-Ti (P-type), high-Ti with high-Cr# (BK-type) and high-Ti with low-Cr# (K-type). MIs of P-type, BK-type and K-type are mostly in compositional ranges of picrite, high TiO2 komatiite (some basalt) and low TiO2 komatiite in Gorgona Island, respectively. Water content of P-type MIs is variable, ranging from 0.05 to 0.9 wt%, whereas those of BK and K-type MIs are limited (500 ppm) do not contain (shrinkage) bubbles and many of them are low in K2O. H2O/K2O, CO2/K2O, S/K2O and F/K2O ratios are positively correlated with Y/Sr ratios, indicating degassing trends of melt at crystallization, magma mixing and/or assimilation. Undegassed H2O/K2O, CO2/K2O, S/K2O and F/K2O ratios of komatiitic (picritic) melt are estimated to be ~10 (~40), ~80 (n.d.), ~7(~3) and ~1(~0.5), respectively, which are much higher than those estimated for the depleted source mantle of the MORB [1.6, 0.7, 1.6 and 0.2, respectively; Salters, V. & Stracke, A. (2004), Composition of the depleted mantle. Geochem. Geophys. Geosys. 5 (2003GC000597)]. The results suggest that Gorgona komatiite and picrite magmas were derived from volatile-rich sources. CO2

The Force of Crystallization and Fracture Propagation during In-Situ Carbonation of Peridotite

Directory of Open Access Journals (Sweden)

Reinier van Noort

2017-10-01

Full Text Available Subsurface mineralization of CO2 by injection into (hydro-fractured peridotites has been proposed as a carbon sequestration method. It is envisaged that the expansion in solid volume associated with the mineralization reaction leads to a build-up of stress, resulting in the opening of further fractures. We performed CO2-mineralization experiments on simulated fractures in peridotite materials under confined, hydrothermal conditions, to directly measure the induced stresses. Only one of these experiments resulted in the development of a stress, which was less than 5% of the theoretical maximum. We also performed one method control test in which we measured stress development during the hydration of MgO. Based on microstructural observations, as well as XRD and TGA measurements, we infer that, due to pore clogging and grain boundary healing at growing mineral interfaces, the transport of CO2, water and solutes into these sites inhibited reaction-related stress development. When grain boundary healing was impeded by the precipitation of silica, a small stress did develop. This implies that when applied to in-situ CO2-storage, the mineralization reaction will be limited by transport through clogged fractures, and proceed at a rate that is likely too slow for the process to accommodate the volumes of CO2 expected for sequestration.

Spinel formation for stabilizing simulated nickel-laden sludge with aluminum-rich ceramic precursors.

Science.gov (United States)

Shih, Kaimin; White, Tim; Leckie, James O

2006-08-15

The feasibility of stabilizing nickel-laden sludge from commonly available Al-rich ceramic precursors was investigated and accomplished with high nickel incorporation efficiency. To simulate the process, nickel oxide was mixed alternatively with gamma-alumina, corundum, kaolinite, and mullite and was sintered from 800 to 1480 degrees C. The nickel aluminate spinel (NiAl2O4) was confirmed as the stabilization phase for nickel and crystallized with efficiencies greater than 90% for all precursors above 1250 degrees C and 3-h sintering. The nickel-incorporation reaction pathways with these precursors were identified, and the microstructure and spinel yield were investigated as a function of sintering temperature with fixed sintering time. This study has demonstrated a promising process for forming nickel spinel to stabilize nickel-laden sludge from a wide range of inexpensive ceramic precursors, which may provide an avenue for economically blending waste metal sludges via the building industry processes to reduce the environmental hazards of toxic metals. The correlation of product textures and nickel incorporation efficiencies through selection of different precursors also provides the option of tailoring property-specific products.

Cations in Octahedral Sites: A Descriptor for Oxygen Electrocatalysis on Transition-Metal Spinels

Energy Technology Data Exchange (ETDEWEB)

Wei, Chao; Feng, Zhenxing; Scherer, Günther G.; Barber, James; Shao-Horn, Yang; Xu, Zhichuan J. (Nanyang); (ICL); (Oregon State U.); (TUM-CREATE); (MIT)

2017-04-10

Exploring efficient and low-cost electrocatalysts for the oxygen-reduction reaction (ORR) and oxygen-evolution reaction (OER) is critical for developing renewable energy technologies such as fuel cells, metal–air batteries, and water electrolyzers. A rational design of a catalyst can be guided by identifying descriptors that determine its activity. Here, a descriptor study on the ORR/OER of spinel oxides is presented. With a series of MnCo2O4, the Mn in octahedral sites is identified as an active site. This finding is then applied to successfully explain the ORR/OER activities of other transition-metal spinels, including MnxCo3-xO4 (x = 2, 2.5, 3), LixMn2O4 (x = 0.7, 1), XCo2O4 (X = Co, Ni, Zn), and XFe2O4 (X = Mn, Co, Ni). A general principle is concluded that the eg occupancy of the active cation in the octahedral site is the activity descriptor for the ORR/OER of spinels, consolidating the role of electron orbital filling in metal oxide catalysis.

RHEED oscillations in spinel ferrite epitaxial films grown by conventional planar magnetron sputtering

Science.gov (United States)

Ojima, T.; Tainosho, T.; Sharmin, S.; Yanagihara, H.

2018-04-01

Real-time in situ reflection high energy electron diffraction (RHEED) observations of Fe3O4, γ-Fe2O3, and (Co,Fe)3O4 films on MgO(001) substrates grown by a conventional planar magnetron sputtering was studied. The change in periodical intensity of the specular reflection spot in the RHEED images of three different spinel ferrite compounds grown by two different sputtering systems was examined. The oscillation period was found to correspond to the 1/4 unit cell of each spinel ferrite, similar to that observed in molecular beam epitaxy (MBE) and pulsed laser deposition (PLD) experiments. This suggests that the layer-by-layer growth of spinel ferrite (001) films is general in most physical vapor deposition (PVD) processes. The surfaces of the films were as flat as the surface of the substrate, consistent with the observed layer-by-layer growth process. The observed RHEED oscillation indicates that even a conventional sputtering method can be used to control film thickness during atomic layer depositions.

RHEED oscillations in spinel ferrite epitaxial films grown by conventional planar magnetron sputtering

Directory of Open Access Journals (Sweden)

T. Ojima

2018-04-01

Full Text Available Real-time in situ reflection high energy electron diffraction (RHEED observations of Fe3O4, γ-Fe2O3, and (Co,Fe3O4 films on MgO(001 substrates grown by a conventional planar magnetron sputtering was studied. The change in periodical intensity of the specular reflection spot in the RHEED images of three different spinel ferrite compounds grown by two different sputtering systems was examined. The oscillation period was found to correspond to the 1/4 unit cell of each spinel ferrite, similar to that observed in molecular beam epitaxy (MBE and pulsed laser deposition (PLD experiments. This suggests that the layer-by-layer growth of spinel ferrite (001 films is general in most physical vapor deposition (PVD processes. The surfaces of the films were as flat as the surface of the substrate, consistent with the observed layer-by-layer growth process. The observed RHEED oscillation indicates that even a conventional sputtering method can be used to control film thickness during atomic layer depositions.

Structural, electronic and magnetic properties of partially inverse spinel CoFe2O4: a first-principles study

International Nuclear Information System (INIS)

Hou, Y H; Liu, Z W; Yu, H Y; Zhong, X C; Qiu, W Q; Zeng, D C; Wen, L S; Zhao, Y J

2010-01-01

Partially inverse spinel CoFe 2 O 4 , which may be prepared through various heat treatments, differs remarkably from the ideal inverse spinel in many properties. The structure of partially inverse spinel CoFe 2 O 4 as well as its electronic and magnetic properties through a systemic theoretical calculation of (Co 1-x Fe x ) Tet (Co x Fe 2-x ) Oct O 4 (x = 0, 0.25, 0.5, 0.75 and 1.0) have been investigated by the generalized gradient approximation (GGA) + U approach. It is found that the Co and Fe ions prefer their high spin configurations with higher spin moments at octahedral sites in all the studied cases, in line with experimental observations. The Co ions at the octahedral sites favour being far away from each other in the partial inverse spinels, which also show half metallicity at certain inversion degrees.

Determination of ferrous and total iron in refractory spinels

Energy Technology Data Exchange (ETDEWEB)

Amonette, J.E. [Physical Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99352 (United States); Matyáš, J. [Material Science Department, Pacific Northwest National Laboratory, Richland, WA 99352 (United States)

2016-03-03

Accurate and precise determination of the redox state of iron (Fe) in spinels presents a significant challenge due to their refractory nature. The resultant extreme conditions needed to obtain complete dissolution generally oxidize some of the Fe(II) initially present and thus prevent the use of colorimetric methods for Fe(II) measurements. To overcome this challenge we developed a hybrid oxidimetric/colorimetric approach, using Ag(I) as the oxidimetric reagent for determination of Fe(II) and 1,10-phenanthroline as the colorimetric reagent for determination of total Fe. This approach, which allows determination of Fe(II) and total Fe on the same sample, was tested on a series of four geochemical reference materials and then applied to the analysis of Fe(Ni) spinel crystals isolated from simulated high-level-waste (HLW) glass and of several reagent magnetites. Results for the reference materials were in excellent agreement with recommended values, with the exception of USGS BIR-1, for which higher Fe(II) values and lower total Fe values were obtained. The Fe(Ni) spinels showed Fe(II) values at the detection limit (ca. 0.03 wt% Fe) and total Fe values higher than obtained by ICP-AES analysis after decomposition by lithium metaborate/tetraborate fusion. For the magnetite samples, total Fe values were in agreement with reference results, but a wide range in Fe(II) values was obtained indicating various degrees of conversion to maghemite. Formal comparisons of accuracy and precision were made with 13 existing methods. Accuracy for Fe(II) and total Fe was at or near the top of the group. Precision varied with the parameter used to measure it but was generally in the middle to upper part of the group for Fe(II) while that for total Fe ranged from the bottom of the group to near the top. - Highlights: • Refractory samples, such as spinels, are the most difficult for Fe redox analysis. • Oxidimetric(Ag{sup +})/colorimetric (phen) method allows analysis of a single

Kinetic model for quartz and spinel dissolution during melting of high-level-waste glass batch

International Nuclear Information System (INIS)

Pokorny, Richard; Rice, Jarrett A.; Crum, Jarrod V.; Schweiger, Michael J.; Hrma, Pavel

2013-01-01

The dissolution of quartz particles and the growth and dissolution of crystalline phases during the conversion of batch to glass potentially affects both the glass melting process and product quality. Crystals of spinel exiting the cold cap to molten glass below can be troublesome during the vitrification of iron-containing high-level wastes. To estimate the distribution of quartz and spinel fractions within the cold cap, we used kinetic models that relate fractions of these phases to temperature and heating rate. Fitting the model equations to data showed that the heating rate, apart from affecting quartz and spinel behavior directly, also affects them indirectly via concurrent processes, such as the formation and motion of bubbles. Because of these indirect effects, it was necessary to allow one kinetic parameter (the pre-exponential factor) to vary with the heating rate. The resulting kinetic equations are sufficiently simple for the detailed modeling of batch-to-glass conversion as it occurs in glass melters. The estimated fractions and sizes of quartz and spinel particles as they leave the cold cap, determined in this study, will provide the source terms needed for modeling the behavior of these solid particles within the flow of molten glass in the melter

Magnesium isotopic composition of the mantle

Science.gov (United States)

Teng, F.; Li, W.; Ke, S.; Marty, B.; Huang, S.; Dauphas, N.; Wu, F.; Helz, R. L.

2009-12-01

Studies of Mg isotopic composition of the Earth not only are important for understanding its geochemistry but also can shed light on the accretion history of the Earth as well as the evolution of the Earth-Moon system. However, to date, the Mg isotopic composition of the Earth is still poorly constrained and highly debated. There is uncertainty in the magnitude of Mg isotope fractionation at mantle temperatures and whether the Earth has a chondritic Mg isotopic composition or not. To constrain further the Mg isotopic composition of the mantle and investigate the behavior of Mg isotopes during igneous differentiation, we report >200 high-precision (δ26Mg French Polynesian volcanoes (Society island and Cook Austral chain); 3) olivine grains from Hawaiian volcanoes (Kilauea, Koolau and Loihi) and 4) peridotite xenoliths from Australia, China, France, Tanzania and USA. Global oceanic basalts and peridotite xenoliths have a limited (<0.2 ‰) variation in Mg isotopic composition, with an average δ26Mg = -0.25 relative to DSM3. Olivines from Hawaiian lavas have δ26Mg ranging from -0.43 to +0.03, with most having compositions identical to basalts and peridotites. Therefore, the mantle’s δ26Mg value is estimated to be ~ -0.25 ± 0.1 (2SD), different from that reported by Wiechert and Halliday (2007; δ26Mg = ~ 0) but similar to more recent studies (δ26Mg = -0.27 to -0.33) (Teng et al. 2007; Handler et al. 2009; Yang et al., 2009). Moreover, we suggest the Earth, as represented by the mantle, has a Mg isotopic composition similar to chondrites (δ26Mg = ~-0.33). The need for a model such as that of Wiechert and Halliday (2007) that involves sorting of chondrules and calcium-aluminum-rich inclusions in the proto planetary disc is thus not required to explain the Mg isotopic composition of the Earth.

The influence of {gamma}-irradiation on electrophysical properties of spinel-based oxide ceramics

Energy Technology Data Exchange (ETDEWEB)

Kovalskiy, A.P.; Shpotyuk, O.I. E-mail: karat@ipm.lviv.ua; Hadzaman, I.V.; Mrooz, O.Ya.; Vakiv, M.M

2000-05-02

The influence of {sup 60}Co {gamma}-irradiation with 1.25 MeV average energy and 1 MGy absorbed dose on electrophysical properties of Cu-, Ni-, Co- and Mn-based spinel ceramic materials in the Cu{sub x}Ni{sub 1-x-y}Co{sub 2y}Mn{sub 2-y}O{sub 4} (0,1{<=}x{<=}0,8;0,1{<=}y{<=}0,9-x) system is investigated. The {gamma}-induced increasing of the electrical resistance is observed for the investigated samples of various compositions. It is supposed that these changes are explained by cationic redistribution in the spinel sublattices of the ceramics.

The influence of γ-irradiation on electrophysical properties of spinel-based oxide ceramics

International Nuclear Information System (INIS)

Kovalskiy, A.P.; Shpotyuk, O.I.; Hadzaman, I.V.; Mrooz, O.Ya.; Vakiv, M.M.

2000-01-01

The influence of 60 Co γ-irradiation with 1.25 MeV average energy and 1 MGy absorbed dose on electrophysical properties of Cu-, Ni-, Co- and Mn-based spinel ceramic materials in the Cu x Ni 1-x-y Co 2y Mn 2-y O 4 (0,1≤x≤0,8;0,1≤y≤0,9-x) system is investigated. The γ-induced increasing of the electrical resistance is observed for the investigated samples of various compositions. It is supposed that these changes are explained by cationic redistribution in the spinel sublattices of the ceramics

Hydration of refractory cements, with spinel phase generated in-situ

International Nuclear Information System (INIS)

Lavat, A.E; Grasselli, M.C; Giuliodori Lovecchio, E

2008-01-01

High alumina refractory materials with additions of synthetic spinel (MgAl 2 O 4 ) have good thermo mechanical and attack from slag properties, which are useful in many technological applications. The spinel phase generated in-situ, MA, has proven to be a suitable and economic alternative to the use of sintered or electrocast spinels. Prior studies have established synthesis conditions for refractory cements with the spinel phase generated in-situ (CCAMA) starting with alumina mixtures and Buenos Aires dolomites. The binding properties of the aluminous cements depend on the hydrated calcium aluminates that form in the setting and hardening stages of the pastes. To avoid breaks, the refractory material must undergo programmed heating before reaching the serviceable temperature. It should also include the present phases and the transformations that occur at different temperatures. In this context knowledge about the green mineral composition and its response to an increase in temperature is especially important. This work presents studies to define the composition of CCAMA cement mortars at different hydration ages, and to estimate phase proportions and behavior during dehydration. DRX and FTIR techniques are applied in order to follow the structural changes that take place during the hydration process. The evolution of the dehydration is also studied, mostly using FTIR. The mortars were prepared with a water/cement ration of 0.5, recommended for this kind of work. The hydration was carried out at room temperature and samples were analyzed at the following ages: 15 min.; 1 h.; 1, 3, 7, 14, 28, 60 and 90 days. With the results the evolution of the phases as a function of the age of the hydration were studied. The main hydrate that was formed was CAH 10 , with a significantly increased proportion during the first 14 days of hydration. Its carbonation was also observed by the presence of calcium carboaluminates and the formation of gibbsite. The MA phase is also

Investigation of spinel-related and orthorhombic LiMNO2 cathodes for rechargeable lithium batteries

CSIR Research Space (South Africa)

Gummow, RJ

1994-05-01

Full Text Available ~ and with carbon at 600~ have been evaluated in rechargeable lithium cells. The cathodes which initially have a composition close to LiMnO2 contain structures related to the lithiated-spinel phase Li2\\[Mn2104 and/or orthorhombic Li... the cathode structure to yield an "over-discharged" state which is possible, for example, with a Lix\\[Mn2104 spinel cathode. 7 Lix\\[Mn2\\]O4 operates at approximately 4 V vs. lithium over the range 0 < x -< 1 and has a...

Nd-isotopes in selected mantle-derived rocks and minerals and their implications for mantle evolution

Science.gov (United States)

Basu, A.R.; Tatsumoto, M.

1980-01-01

The Sm-Nd systematics in a variety of mantle-derived samples including kimberlites, alnoite, carbonatite, pyroxene and amphibole inclusions in alkali basalts and xenolithic eclogites, granulites and a pyroxene megacryst in kimberlites are reported. The additional data on kimberlites strengthen our earlier conclusion that kimberlites are derived from a relatively undifferentiated chondritic mantle source. This conclusion is based on the observation that the e{open}Nd values of most of the kimberlites are near zero. In contrast with the kimberlites, their garnet lherzolite inclusions show both time-averaged Nd enrichment and depletion with respect to Sm. Separated clinopyroxenes in eclogite xenoliths from the Roberts Victor kimberlite pipe show both positive and negative e{open}Nd values suggesting different genetic history. A whole rock lower crustal scapolite granulite xenolith from the Matsoku kimberlite pipe shows a negative e{open}Nd value of -4.2, possibly representative of the base of the crust in Lesotho. It appears that all inclusions, mafic and ultramafic, in kimberlites are unrelated to their kimberlite host. The above data and additional Sm-Nd data on xenoliths in alkali basalts, alpine peridotite and alnoite-carbonatites are used to construct a model for the upper 200 km of the earth's mantle - both oceanic and continental. The essential feature of this model is the increasing degree of fertility of the mantle with depth. The kimberlite's source at depths below 200 km in the subcontinental mantle is the most primitive in this model, and this primitive layer is also extended to the suboceanic mantle. However, it is clear from the Nd-isotopic data in the xenoliths of the continental kimberlites that above 200 km the continental mantle is distinctly different from their suboceanic counterpart. ?? 1980 Springer-Verlag.

New constraints on the evolution of the Gibraltar Arc from palaeomagnetic data of the Ceuta and Beni Bousera peridotites (Rif, northern Africa)

Science.gov (United States)

Berndt, Thomas; Ruiz-Martínez, Vicente Carlos; Chalouan, Ahmed

2015-03-01

The Betic Cordillera and the Moroccan Rif together form one of the smallest and tightest orogenic arcs on Earth and almost completely close the Mediterranean to the west. For the explanation of the geodynamic evolution of the mountain belt, palaeomagnetic data that generally found clockwise block rotations in the Iberian and anticlockwise rotations in the Moroccan part of the mountain belt, have played a key role in recent works. This palaeomagnetic study has found new constraints on the rotations and timing of the peridotitic bodies outcropping in the key position at the westernmost margin of the mountain belt, in Ceuta and Beni Bousera (Rif, northern Africa). Detailed thermal demagnetization of 115 individually oriented samples from 14 sites was combined with rock magnetic and scanning electron microscopic experiments to analyze the magnetic mineralogy responsible for the remanences and the mechanisms and relative times of their acquisition. In Ceuta, up to three magnetic components, and in Beni Bousera, up to two magnetic components have been found, that are all to be interpreted as chemical remanent magnetizations (CRM). The data suggests the following succession of geodynamic events affecting the peridotites until recent times: (1) after their exhumation and subsequent cooling about 20 Ma ago, they recorded a characteristic remanent magnetization of both normal and reversed polarities, carried by (pseudo-)single-domain magnetite grains; (2) after their dismembering, the Ceuta peridotites were tilted southward by 22-34° about a horizontal or tilted axis (up to plunge 50°) with an azimuth of 72-145° and the Beni Bousera peridotites were rotated anticlockwise by 72.3 ± 12.1° about a vertical axis and (3) both recorded another magnetic signal of normal polarity only, carried by multi-domain magnetite grains; and finally (4) the Ceuta peridotites rotated anticlockwise by 19.7 ± 5.9° about a vertical axis. This study provides the first palaeomagnetic data for

Compositional controls on spinel clouding and garnet formation in plagioclase of olivine metagabbros, Adirondack Mountains, New York

Science.gov (United States)

McLelland, J.M.; Whitney, P.R.

1980-01-01

Olivine metagabbros from the Adirondacks usually contain both clear and spinel-clouded plagioclase, as well as garnet. The latter occurs primarily as the outer rim of coronas surrounding olivine and pyroxene, and less commonly as lamellae or isolated grains within plagioclase. The formation of garnet and metamorphic spinel is dependent upon the anorthite content of the plagioclase. Plagioclase more sodic than An38??2 does not exhibit spinel clouding, and garnet rarely occurs in contact with plagioclase more albitic than An36??4. As a result of these compositional controls, the distribution of spinel and garnet mimics and visually enhances original igneous zoning in plagioclase. Most features of the arrangement of clear (unclouded) plagioclase, including the shells or moats of clear plagioclase which frequently occur inside the garnet rims of coronas, can be explained on the basis of igneous zoning. The form and distribution of the clear zones may also be affected by the metamorphic reactions which have produced the coronas, and by redistribution of plagioclase in response to local volume changes during metamorphism. ?? 1980 Springer-Verlag.

On the nature and origin of garnet in highly-refractory Archean lithosphere: implications for continent stabilisation

Science.gov (United States)

Gibson, Sally

2014-05-01

The nature and timescales of garnet formation in the Earth's subcontinental lithospheric mantle (SCLM) are important to our understanding of how this rigid outer shell has evolved and stabilised since the Archean. Nevertheless, the widespread occurrence of pyrope garnet in the sub-cratonic mantle remains one of the 'holy grails' of mantle petrology. The paradox is that garnet often occurs in mantle lithologies (dunites and harzburgites) which represent residues of major melting events (up to 40 %) whereas experimental studies on fertile peridotite suggest this phase should be exhausted by years. The garnets display systematic trends from ultra-depleted to enriched compositions that have not been recognised in peridotite suites from elsewhere (Gibson et al., 2013). Certain harzburgite members of the xenolith suite contain the first reported occurrence of pyrope garnets with rare-earth element (REE) patterns similar to hypothetical garnets proposed by Stachel et al. (2004) to have formed in the Earth's SCLM during the Archean, prior to metasomatism. These rare ultra-depleted low-Cr garnets occur in low temperature (~1050 oC) xenoliths derived from depths of ~120 km and coexist in chemical and textural equilibrium with highly-refractory olivine (Fo95.4) and orthopyroxene (Mg#=96.4). These phases are all more magnesian than generally encountered in global samples of depleted mantle, i.e. harzburgites and diamond inclusion suites. The Tanzanian ultra-depleted garnets form interconnecting networks ('necklaces') around grains of orthopyroxene, which is of key importance to their origin. This close spatial relationship of garnet and orthopyroxene together with the major, trace and REE contents of the ultra-depleted garnets, are consistent with an origin by isochemical exsolution. The significance of ultra-depleted low-Cr garnets has not previously been recognised in global suites of mantle xenoliths or diamond inclusions: they appear to have been overlooked, primarily

Evidence of Arc Magma Genesis in a Paleo-Mantle Wedge, the Higashi-Akaishi Peridotite, Japan

Science.gov (United States)

Till, C. B.; Guild, M. R.; Grove, T. L.; Carlson, R. W.

2014-12-01

Located in the Sanbagawa subduction-related high-pressure metamorphic belt in SW Japan on the island of Shikoku, the Higashi-akaishi peridotite body is composed of dunite, lherzolite and garnet clinopyroxenite, interfingered in one locality with quartz-rich eclogite. Previous work indicates the P-T history of the peridotite includes rapid prograde metamorphism with peak temperatures of 700-810°C and pressures of 2.9-3.8 GPa [1] at ~88-89 Ma followed by rapid exhumation at >2.5 cm/yr [2,3]. Major and trace element and isotopic data from samples within the Higashi-akaishi peridotite presented here and in another recent study [4] provide a record of subduction zone melting processes in a paleo-mantle wedge. Ultramafic samples range from 40-52 wt.% SiO2, 1-11 wt.% Al2O3 and 21-45 wt.% MgO with olivine and clinopyroxene Mg#'s as high as 0.93. The quartz-rich eclogite contains 62 wt.% SiO2, 6 wt.% MgO and 13 wt.% Al2O3 with trace element concentrations that are enriched relative to the ultramafic samples. 87Sr/86Sr (.703237-.704288), 143Nd/144Nd (ɛNd=+2 to +6) and Pb isotopic compositions are within the range of previously studied Japanese arc rocks. We interpret the pyroxenites as shallowly crystallized cumulates with varying amounts of trapped hydrous melt and the harzburgites as residues of melting. The peak P-T conditions of these rocks are similar to the solidus conditions of H2O-saturated fertile mantle near the base of the mantle wedge [5,6]. The presence of garnet porphyroblasts that enclose primary euhedral chlorite together with the chemical evidence, suggest these samples are associated with mantle melting in the presence of H2O. Major element modeling suggests the quartz-rich eclogite composition can be reproduced through mixing melts of subducted sediment with wet peridotite melts in the mantle wedge. Thus the Higashi-aikashi rock suite provides an in-situ record of the beginnings of hydrous melting and the mechanisms of metasomatism in the mantle wedge

Identification of Spinel Iron Oxide Nanoparticles by 57Fe NMR

Directory of Open Access Journals (Sweden)

SangGap Lee

2011-12-01

Full Text Available We have synthesized and studied monodisperse iron oxide nanoparticles of smaller than 10 nm to identify between the two spinel phases, magnetite and maghemite. It is shown that 57Fe NMR spectroscopy is a promising tool for distinguishing between the two phases.

Effect of cutting edge radius on surface roughness in diamond tool turning of transparent MgAl2O4 spinel ceramic

Science.gov (United States)

Yue, Xiaobin; Xu, Min; Du, Wenhao; Chu, Chong

2017-09-01

Transparent magnesium aluminate spinel (MgAl2O4) ceramic is one of an important optical materials. However, due to its pronounced hardness and brittleness, the optical machining of this material is very difficult. Diamond turning has advantages over the grinding process in flexibility and material removal rate. However, there is a lack of research that could support the use of diamond turning technology in the machining of MgAl2O4 spinel ceramic. Using brittle-ductile transition theory of brittle material machining, this work provides critical information that may help to realize ductile-regime turning of MgAl2O4 spinel ceramic. A characterization method of determination the cutting edge radius is introduced here. Suitable diamond tools were measured for sharpness and then chosen from a large number of candidate tools. The influence of rounded cutting edges on surface roughness of the MgAl2O4 spinel ceramic is also investigated. These results indicate that surface quality of MgAl2O4 spinel is relate to the radius of diamond tool's cutting edge, cutting speed, and feed rate. Sharp diamond tools (small radius of cutting edge) facilitated ductile-regime turning of MgAl2O4 spinel and shows great potential to reduce surface roughness and produce smoother final surface.

Influence of graphite contamination on the optical properties of transparent spinel obtained by spark plasma sintering

International Nuclear Information System (INIS)

Bernard-Granger, G.; Benameur, N.; Guizard, C.; Nygren, M.

2009-01-01

The optical properties of transparent spinel sintered by spark plasma sintering have been investigated for incident electromagnetic radiations with wavelengths in the range 0.2-2 μm. It is shown that residual porosities and second-phase graphite particles have a strong influence on the in-line transmittance. Because of the graphite particles, the in-line transmittance measured does not approach that of monocrystalline spinel for wavelengths above 1 μm

Subsolidus Evolution of the Magnetite-Spinel-UlvöSpinel Solid Solutions in the Kovdor Phoscorite-Carbonatite Complex, NW Russia

Directory of Open Access Journals (Sweden)

Gregory Yu. Ivanyuk

2017-11-01

Full Text Available The Kovdor phoscorite-carbonatite ore-pipe rocks form a natural series, where apatite and magnetite first gradually increase due to the presence of earlier crystallizing forsterite in the pipe marginal zone and then decrease as a result of carbonate development in the axial zone. In all lithologies, magnetite grains contain (oxyexsolution inclusions of comparatively earlier ilmenite group minerals and/or later spinel, and their relationship reflects the concentric zonation of the pipe. The temperature and oxygen fugacity of titanomagnetite oxy-exsolution decreases in the natural rock sequence from about 500 °C to about 300 °C and from NNO + 1 to NNO − 3 (NNO is Ni-NiO oxygen fugacity buffer, with a secondary positive maximum for vein calcite carbonatite. Exsolution spinel forms spherical grains, octahedral crystals, six-beam and eight-beam skeletal crystals co-oriented with host magnetite. The ilmenite group minerals occur as lamellae oriented along {111} and {100} planes of oxy-exsolved magnetite. The kinetics of inclusion growth depends mainly on the diffusivity of cations in magnetite: their comparatively low diffusivities in phoscorite and carbonatites of the ore-pipe internal part cause size-independent growth of exsolution inclusions; while higher diffusivities of cations in surrounding rocks, marginal forsterite-rich phoscorite and vein calcite carbonatite result in size-dependent growth of inclusions.

Effect of mulitivalent cation dopants on lithium manganese spinel cathodes

CSIR Research Space (South Africa)

De Kock, A

1998-02-01

Full Text Available The aim of this investigation is to determine optimised spinel cathode compositions that can be used in lithium cells. The cycling stability of 4 V LixMn2O4 electrodes in lithium, flooded electrolyte glass cells has been improved by the addition...

Direct observation of cation distributions of ideal inverse spinel CoFe2O4 nanofibres and correlated magnetic properties

KAUST Repository

Zeng, Xue; Zhang, Junwei; Zhu, Shimeng; Deng, Xia; Ma, Hongbin; Zhang, Junli; Zhang, Qiang; Li, Peng; Xue, Desheng; Mellors, Nigel J; Zhang, Xixiang; Peng, Yong

2017-01-01

multiferroic heterostructures. Although we know that the distribution of cations (Fe3+ and Co2+) in a spinel structure governs its magnetic properties, their distribution in the so-called ideal inverse spinel structure of a ferrite, CoFe2O4, has not yet been

Spinel and orthopyroxene exsolved from clinopyroxene in the Haladala pluton in the middle Tianshan (Xinjiang, China)

Science.gov (United States)

Zhu, Yongfeng; Chen, Jing; Xue, Yunxin; Feng, Wanyi; Jiang, Jiuyang

2017-12-01

The Haladala pluton, consisting of troctolite, olivine gabbro and gabbro with zircon SHRIMP U-Pb age of 309 ± 2 Ma (MSWD = 0.72), intruded the Devonian-Carboniferous arc segments in the middle Tianshan. Amphibole, coexisting with magnetite, amphibole, and phlogopite, crystallized in a magma chamber at depth of 20 km (6.9-7.4 kbar, 934-943 °C) based on various thermobaramoters. Two kinds of exsolution textures (spinel rods in clinopyroxene, orthopyroxene lamellae in clinopyroxene) occur in troctolite and olivine gabbro. We describe oriented spinel rods and orthopyroxene lamellae exsolved from the host clinopyroxene based on optical and high-resolution transmission electron microscope (HRTEM) observations. The spinel rods (100) are parallel to their host clinopyroxene (010). Orthopyroxene lamellae (010) are coherent and strictly parallel to their host clinopyroxene (010). Exsolution of spinel rods from the host clinopyroxene is controlled by the reaction of (Ca0.5M2+ 0.5)Fe3+[AlSiO6]in clinopyroxene → (Ca0.86-0.17M2+ 0.14-0.17)(M2 + 1.00-0.96Al0-0.04)[Al0.17-0.10Si1.83-1.90O6] + Fe3O4 + O2.

EPR, mu-Raman and Crystallographic properties of spinel type ZnCr{sub 2}O{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Vargas-Hernandez, C; Almanza, O; Jurado, J F, E-mail: cvargash@unal.edu.c [Universidad Nacional de Colombia, Manizales-Colombia Laboratorio de Propiedades Opticas de Materiales-POM (Colombia)

2009-05-01

Structural, vibrational and electron paramagnetic resonance (EPR) analysis for compound ZnCr{sub 2}O{sub 4} are shown in this work. These types of materials are used in technological applications as humidity sensors and piezoelectric devices. The compound was obtained by mean of solid state reaction technique from binary precursors ZnO and Cr{sub 2}O{sub 3}. After three thermal treatments the sample structure was monitoring using X ray diffraction (XRD), the spinel cubic phase has been indexed within O{sup 7}{sub h}(Fd3m) spatial group. It is observed normal spinel phase. Micro-Raman analysis revealed bands for normal vibration modes of Zn and Cr atoms in tetrahedral and octahedral environments formed by oxygen atoms at approximately 400 and 900 cm{sup -1}, respectively. Bands around 941 cm{sup -1} are associated possibly to vacancies in the tetrahedral and octahedral sites due to interaction between Zn and Cr ions. EPR signal from 150 to 300 K isothermals indicates a transition between inverse spinel to normal spinel type in a central field around 3350 G. A signal at approximately 3400 G corresponding to the C'r{sup +3} in tetrahedral sites is observed near the central field.

High-pressure phase of the cubic spinel NiMn2O4

DEFF Research Database (Denmark)

Åsbrink, S.; Waskowska, A.; Olsen, J. Staun

1998-01-01

experimental uncertainty, there is no volume change at the transition. The cia ratio of the tetragonal spinel is almost independent of pressure and equal to 0.91. The phase transition is attributed to the Jahn-Teller-type distortion and the ionic configurationcan be assumed as (Mn3+)(tetr)[Ni2+Mn3+](oct......It has been observed that the fee spinel NiMn2O4 transforms to a tetragonal structure at about 12 GPa. The tetragonal phase does not revert to the cubic phase upon decompression and its unit-cell constants at ambient pressure are a(0)=8.65(8) and c(0)=7.88(15) Angstrom (distorted fee). Within thr......). The bulk modulus of the cubic phase is 206(4) GPa....

Lattice vibrations of materials for lithium rechargeable batteries II. Lithium extraction-insertion in spinel structures

International Nuclear Information System (INIS)

Julien, C.M.; Camacho-Lopez, M.A.

2004-01-01

Lithiated spinel manganese oxides with various amounts of lithium have been prepared through solid-state reaction and electrochemical intercalation and deintercalation. Local structure of the samples are studied using Raman scattering and Fourier transform infrared spectroscopy. We report vibrational spectra of lithiated manganese oxides Li x Mn 2 O 4 as a function of lithium concentration in the range 0.1≤x≤2.0. Raman and Fourier transform infrared (FTIR) spectral results indicated multiple-phase reactions when the lithium content is modified in the spinel lattice. Lattice dynamics of lithiated spinel manganese oxides have been interpreted using either a classical factor-group analysis or a local environment model. The structural modifications have been studied on the basis of vibrations of LiO 4 tetrahedral and MnO 6 octahedral units when Li/Mn≤0.5, and LiO 4 , LiO 6 , and MnO 6 structural units when Li/Mn>0.5

Synthesis of ultrasmall Li-Mn spinel oxides exhibiting unusual ion exchange, electrochemical, and catalytic properties

Science.gov (United States)

Miyamoto, Yumi; Kuroda, Yoshiyuki; Uematsu, Tsubasa; Oshikawa, Hiroyuki; Shibata, Naoya; Ikuhara, Yuichi; Suzuki, Kosuke; Hibino, Mitsuhiro; Yamaguchi, Kazuya; Mizuno, Noritaka

2015-10-01

The efficient surface reaction and rapid ion diffusion of nanocrystalline metal oxides have prompted considerable research interest for the development of high functional materials. Herein, we present a novel low-temperature method to synthesize ultrasmall nanocrystalline spinel oxides by controlling the hydration of coexisting metal cations in an organic solvent. This method selectively led to Li-Mn spinel oxides by tuning the hydration of Li+ ions under mild reaction conditions (i.e., low temperature and short reaction time). These particles exhibited an ultrasmall crystallite size of 2.3 nm and a large specific surface area of 371 ± 15 m2 g-1. They exhibited unique properties such as unusual topotactic Li+/H+ ion exchange, high-rate discharge ability, and high catalytic performance for several aerobic oxidation reactions, by creating surface phenomena throughout the particles. These properties differed significantly from those of Li-Mn spinel oxides obtained by conventional solid-state methods.

Synthesis of ultrasmall Li–Mn spinel oxides exhibiting unusual ion exchange, electrochemical, and catalytic properties

Science.gov (United States)

Miyamoto, Yumi; Kuroda, Yoshiyuki; Uematsu, Tsubasa; Oshikawa, Hiroyuki; Shibata, Naoya; Ikuhara, Yuichi; Suzuki, Kosuke; Hibino, Mitsuhiro; Yamaguchi, Kazuya; Mizuno, Noritaka

2015-01-01

The efficient surface reaction and rapid ion diffusion of nanocrystalline metal oxides have prompted considerable research interest for the development of high functional materials. Herein, we present a novel low-temperature method to synthesize ultrasmall nanocrystalline spinel oxides by controlling the hydration of coexisting metal cations in an organic solvent. This method selectively led to Li–Mn spinel oxides by tuning the hydration of Li+ ions under mild reaction conditions (i.e., low temperature and short reaction time). These particles exhibited an ultrasmall crystallite size of 2.3 nm and a large specific surface area of 371 ± 15 m2 g−1. They exhibited unique properties such as unusual topotactic Li+/H+ ion exchange, high-rate discharge ability, and high catalytic performance for several aerobic oxidation reactions, by creating surface phenomena throughout the particles. These properties differed significantly from those of Li–Mn spinel oxides obtained by conventional solid-state methods. PMID:26456216

Zn{sub x-1}Cu{sub x}Mn{sub 2}O{sub 4} spinels; synthesis, structural characterization and electrical evaluation

Energy Technology Data Exchange (ETDEWEB)

Mendez M, F.; Lima, E.; Bosch, P.; Pfeiffer, H. [UNAM, Instituto de Investigaciones en Materiales, Circuito Exterior, Ciudad Universitaria, 04510 Mexico D. F. (Mexico); Gonzalez, F., E-mail: pfeiffer@iim.unam.m [Universidad Autonoma Metropolitana, Unidad Iztapalapa, Av. San Rafael Atlixco No. 186, Col. Vicentina, 09340 Mexico D. F. (Mexico)

2010-07-01

This work presents the structural characterization and electrical evaluation of Zn{sub x-1}Cu{sub x}Mn{sub 2}O{sub 4} spinels, which are materials presented as secondary phases into the vari stor ceramic systems. Samples were analyzed by X-ray diffraction, solid-state nuclear magnetic resonance, infrared spectroscopy, scanning electron microscopy and impedance spectroscopy. Although, the addition of copper to the ZnMn{sub 2}O{sub 4} spinel did not produce morphological changes, the structure and electrical behaviors changed considerably. Structurally, copper addition induced the formation of partial inverse spinels, and its addition increases significantly the electrical conductivity. Therefore, the formation of Zn{sub x-1}Cu{sub x}Mn{sub 2}O{sub 4} spinels, as secondary phases into the vari stor materials, may compromise significantly the vari stor efficiency. (Author)

Effect of oxygen fugacity on OH dissolution in olivine under peridotite-saturated conditions: An experimental study at 1.5-7 GPa and 1100-1300 °C

Science.gov (United States)

Yang, Xiaozhi

2016-01-01

The dissolution of OH in olivine by experimental studies at simulated conditions has attracted increasing interest over the past three decades, and the influence of pressure, temperature and composition has been relatively well constrained. Oxygen fugacity is highly heterogeneous in the upper mantle, on both temporal and spatial scales, and is an important parameter in characterizing many chemical and physical processes in the mantle. However, less attention has been devoted to the effect of oxygen fugacity on OH dissolution in olivine, and the only few available reports on this topic have led to significant inconsistency and debate. In this study, the correlation between oxygen fugacity and OH solubility in Fe-bearing olivine has been systematically investigated by conducting experiments at 1.5-7 GPa and 1100-1300 °C and under peridotite- and fluid-saturated conditions, with natural gem-quality olivine single crystals and fresh peridotite xenoliths as starting materials and with oxygen fugacity controlled by the Fe-FeO, Ni-NiO and Fe2O3-Fe3O4 oxygen buffer pairs. The water concentrations were determined by polarized analyses using a Fourier-transform infrared spectroscopy. The results show that, at all the experimental conditions, the OH bands at both high frequency (∼3650-3450 cm-1) and low frequency (∼3450-3100 cm-1) are prominent. The intensity of OH bands at ∼3355 and 3325 cm-1 increases positively with oxygen fugacity, suggesting a dominant role of Fe3+ in their incorporation. Under otherwise identical conditions, the water content is gradually enhanced with increasing pressure, temperature or oxygen fugacity. The effect of oxygen fugacity on the enhancement of OH solubility appears not sensitive to temperature (1100-1300 °C) at a given pressure, but becomes progressively stronger with increasing pressure from 1.5 to 7 GPa given the temperature. Relative to oxygen fugacity buffers, the OH solubility is on average increased by ∼50% between Fe-FeO and

Effect of MgCl2 addition on the sintering behavior of MgAl2O4 spinel and formation of nano-particles

Directory of Open Access Journals (Sweden)

Mohammadi F.

2014-01-01

Full Text Available In this paper, the effect of MgCl2 addition on the sintering behavior of MgAl2O4 spinel produced via oxide mixture method was investigated. For this reason, the stoichiometric mixture of magnesite and calcined alumina as raw materials was calcined at 1100°C. The calcined mixture was milled, pressed and then, fired at 1300 and 1500°C after addition of various amounts of MgCl2. Besides, the physical properties, phase composition and microstructure of fired samples were investigated. The results showed that MgCl2 addition has great effect on the densification and particle size of spinel. Besides, MgCl2 addition increases the amount of spinel phase at all firing temperatures. Due to the decomposition of MgCl2 and then formation of ultra-fine MgO particles, the nano-sized spinel is formed on the surface of the larger spinel particles.

Serpentinization of mantle-derived peridotites at mid-ocean ridges: Mesh texture development in the context of tectonic exhumation

Science.gov (United States)

Rouméjon, Stéphane; Cannat, Mathilde

2014-06-01

At slow spreading ridges, axial detachment faults exhume mantle-derived peridotites and hydrothermal alteration causes serpentinization in a domain extending more than 1 km next to the fault. At the microscopic scale, serpentinization progresses from a microfracture network toward the center of olivine relicts and forms a mesh texture. We present a petrographic study (SEM, EBSD, and Raman) of the serpentine mesh texture in a set of 278 abyssal serpentinized peridotites from the Mid-Atlantic and Southwest Indian Ridges. We show that serpentinization initiated along two intersecting sets of microfractures that have consistent orientations at the sample scale, and in at least one studied location, at the 100 m scale. We propose that these microfractures formed in fresh peridotites due to combined thermal and tectonic stresses and subsequently served as channels for serpentinizing fluids. Additional reaction-induced cracks developed for serpentinization extents <20%. The resulting microfracture network has a typical spacing of ˜60 µm but most serpentinization occurs next to a subset of these microfractures that define mesh cells 100-400 µm in size. Apparent mesh rim thickness is on average 33 ± 19 µm corresponding to serpentinization extents of 70-80%. Published laboratory experiments suggest that mesh rims formation could be completed in a few years (i.e., quasi instantaneous at the plate tectonic timescale). The depth and extent of the serpentinization domain in the detachment fault's footwall are probably variable in time and space and as a result we expect that the serpentine mesh texture at slow spreading ridges forms at variable rates with a spatially heterogeneous distribution.

Characterization of Organic Materials in the Xenolithic Clasts in Sharps (H3.4) Meteorite Using Microraman Spectroscopy

Science.gov (United States)

Chan, Q. H. S.; Zolensky, M. E.; Bodnar, R. J.; Kebukawa, Y.

2015-01-01

Graphitization of carbon is an irreversible process which alters the structure of graphitic materials in response to the increase in metamorphic grade (temperature and/or pressure). Carbonaceous materials offer a reliable geothermometer as their Raman spectra change systematically with increasing metamorphic grade [1-3]. In this study, we identified carbonaceous materials in the xenolithic clasts in Sharps and interpreted their metamorphic history by revealing the structural organization (order) of the polyaromatic organic phases using µ-Raman spectroscopy.

A series of spinel phase cathode materials prepared by a simple hydrothermal process for rechargeable lithium batteries

Science.gov (United States)

Liang, Yan-Yu; Bao, Shu-Juan; Li, Hu-Lin

2006-07-01

A series of spinel-structured materials have been prepared by a simple hydrothermal procedure in an aqueous medium. The new synthetic method is time and energy saving i.e., no further thermal treatment and extended grinding. The main experimental process involved the insertion of lithium into electrolytic manganese dioxide with glucose as a mild reductant in an autoclave. Both the hydrothermal temperature and the presence of glucose play the critical roles in determining the final spinel integrity. Particular electrochemical performance has also been systematically explored, and the results show that Al 3+, F - co-substituted spinels have the best combination of initial capacity and capacity retention among all these samples, exhibited the initial capacity of 115 mAh/g and maintained more than 90% of the initial value at the 50th cycle.

Phase relations and Gibbs energies of spinel phases and solid solutions in the system Mg-Rh-O

Energy Technology Data Exchange (ETDEWEB)

Jacob, K.T., E-mail: katob@materials.iisc.ernet.in [Department of Materials Engineering, Indian Institute of Science, Bangalore 560 012 (India); Prusty, Debadutta [Department of Materials Engineering, Indian Institute of Science, Bangalore 560 012 (India); Kale, G.M. [Institute for Materials Research, University of Leeds, Leeds, LS2 9JT (United Kingdom)

2012-02-05

Highlights: Black-Right-Pointing-Pointer Refinement of phase diagram for the system Mg-Rh-O and thermodynamic data for spinel compounds MgRh{sub 2}O{sub 4} and Mg{sub 2}RhO{sub 4} is presented. Black-Right-Pointing-Pointer A solid-state electrochemical cell is used for thermodynamic measurement. Black-Right-Pointing-Pointer An advanced design of the solid-state electrochemical cell incorporating buffer electrodes is deployed to minimize polarization of working electrode. Black-Right-Pointing-Pointer Regular solution model for the spinel solid solution MgRh{sub 2}O{sub 4} - Mg{sub 2}RhO{sub 4} based on ideal mixing of cations on the octahedral site is proposed. Black-Right-Pointing-Pointer Factors responsible for stabilization of tetravalent rhodium in spinel compounds are identified. - Abstract: Pure stoichiometric MgRh{sub 2}O{sub 4} could not be prepared by solid state reaction from an equimolar mixture of MgO and Rh{sub 2}O{sub 3} in air. The spinel phase formed always contained excess of Mg and traces of Rh or Rh{sub 2}O{sub 3}. The spinel phase can be considered as a solid solution of Mg{sub 2}RhO{sub 4} in MgRh{sub 2}O{sub 4}. The compositions of the spinel solid solution in equilibrium with different phases in the ternary system Mg-Rh-O were determined by electron probe microanalysis. The oxygen potential established by the equilibrium between Rh + MgO + Mg{sub 1+x}Rh{sub 2-x}O{sub 4} was measured as a function of temperature using a solid-state cell incorporating yttria-stabilized zirconia as an electrolyte and pure oxygen at 0.1 MPa as the reference electrode. To avoid polarization of the working electrode during the measurements, an improved design of the cell with a buffer electrode was used. The standard Gibbs energies of formation of MgRh{sub 2}O{sub 4} and Mg{sub 2}RhO{sub 4} were deduced from the measured electromotive force (e.m.f.) by invoking a model for the spinel solid solution. The parameters of the model were optimized using the measured

Subduction factory in an ampoule: Experiments on sediment-peridotite interaction under temperature gradient conditions

Science.gov (United States)

Woodland, A. B.; Bulatov, V. K.; Brey, G. P.; Girnis, A. V.; Höfer, H. E.; Gerdes, A.

2018-02-01

To better understand processes above subducted oceanic slabs, we have undertaken experiments with juxtaposed sediment and peridotite layers at pressures of 7.5 and 10.5 GPa at a controlled temperature gradient from ∼100 to ∼500 °C per a sample length of ∼3 mm. The sediment starting material contains H2O (6.9 wt%) and CO2 (5.9 wt%) and has a major-element composition similar to GLOSS (Plank and Langmuir, 1998) doped with trace elements at 10-100 ppm levels. Several experiments were conducted with ∼0.5 wt% Cl or F. The peridotite layer is composed of natural olivine (66 wt%), orthopyroxene (27 wt%) and garnet (7 wt%) mixed with ∼15 wt% graphite. Several experimental configurations were investigated, but the "basic" setup has the sediment layer at the bottom in the cold zone (400-1200 °C) overlain by peridotite at 900-1500 °C. The temperature distribution was determined by two thermocouples and orthopyroxene-garnet thermometry. Features common to many experiments are (1) the development of multiple layers of various lithologies and a pool of hydrous silicate or carbonate-silicate melt in the hottest part of the capsule; (2) replacement of olivine by orthopyroxene in the metaperidotite; (3) preservation and growth of garnet and local development of magnesite in the metaperidotite layer; (4) enrichment in garnet within the metasediment layer at the contact with the metaperidotite; (5) formation of a clinopyroxene-garnet assemblage at the bottom (the coldest part); (6) presence of K-bearing phases (phlogopite or phengite) and carbonates in the metasediment layer only at temperatures Ca are largely retained in the coldest part of the metasediment layer in clinopyroxene, Ca-rich garnet and aragonite. The melt is a product of interaction between partial melt or fluid from the sediment and peridotite. It has a silico-carbonatite composition with variable SiO2, MgO, FeO and CaO contents and low Al2O3. The addition of Cl has almost no effect on element

The Effect of CO2 on Partial Reactive Crystallization of MORB-Eclogite-derived Basaltic Andesite in Peridotite and Generation of Silica-Undersaturated Basalts

Science.gov (United States)

Mallik, A.; Dasgupta, R.

2012-12-01

Recycled oceanic crust (MORB-eclogite) is considered to be the dominant heterogeneity in Earth's mantle. Because MORB-eclogite is more fusible than peridotite, siliceous partial melt derived from it must react with peridotite while the latter is still in the subsolidus state. Thus, studying such reactive process is important in understanding melting dynamics of the Earth's mantle. Reaction of MORB-eclogite-derived andesitic partial melt with peridotite can produce alkalic melts by partial reactive crystallization but these melts are not as silica-undersaturated as many natural basanites, nephelinites or melititites [1]. In this study, we constrain how dissolved CO2 in a siliceous MORB-eclogite-derived partial melt affects the reaction phase equilibria involving peridotite and can produce nephelinitic melts. Here we compare experiments on CO2-free [1] and 2.6 wt.% CO2 bearing andesitic melt+lherzolite mixtures conducted at 1375 °C and 3 GPa with added melt fraction of 8-50 wt.%. In both CO2-free and CO2-bearing experiments, melt and olivine are consumed and opx and garnet are produced, with the extent of modal change for a given melt-rock ratio being greater for the CO2-bearing experiments. While the residue evolves to a garnet websterite by adding 40% of CO2-bearing melt, the residue becomes olivine-free by adding 50% of the CO2-free melt. Opx mode increases from 12 to ~55 wt.% for 0 to 40% melt addition in CO2-bearing system and 12 to ~43 wt.% for 0 to 50% melt addition in CO2-free system. Garnet mode, for a similar range of melt-rock ratio, increases from ~10 to ~15 wt.% for CO2 bearing system and to ~11 wt.% for CO2-free system. Reacted melts from 25-33% of CO2-bearing melt-added runs contain ~39 wt.% SiO2 , ~11-13 wt.% TiO2, ~9 wt.% Al2O3, ~11 wt.% FeO*, 16 wt.% MgO, 10-11 wt.% CaO, and 3 wt.% Na2O whereas experiments with a similar melt-rock ratio in a CO2-free system yield melts with 44-45 wt.% SiO2, 6-7 wt.% TiO2, 13-14 wt.% Al2O3, 10-11 wt.% FeO*, 12-13 wt

DT fusion neutron irradiation of BNL--LASL superconductor wires, LASL YAG, Al2O3 and Spinel, LASL-IIT MgO, YAG, Al2O3 and Spinel, and NRL GeO2 crystals, December 28, 1977

International Nuclear Information System (INIS)

MacLean, S.C.

1978-01-01

The DT fusion neutron irradiation of eleven BNL-LAST superconductor wires, six NRL GeO 2 crystals, two YAG, two Spinel and two Al 2 O 3 crystals for LASL and four LASL high purity single crystals of MgO, YAG, Spinel and Al 2 O 3 is described. The sample position, beam-on time, and neutron dose record are given. The maximum fluence on any sample was 1.51 x 10 16 neutrons/cm 2

Long wavelength magnetic anomalies over continental rifts in cratonic region

Science.gov (United States)

Friedman, S. A.; Persaud, P.; Ferre, E. C.; Martín-Hernández, F.; Feinberg, J. M.

2017-12-01

New collections of unaltered mantle xenoliths shed light on potential upper mantle contributions to long wavelength magnetic anomalies (LWMA) in continental rifts in cratonic / shield areas. The new material originates from the East African Rift (Tanzania), the Rio Grande Rift (U.S.A.), the Rhine Rift (Germany), and the West Antarctic Rift (Antarctica). The xenoliths sample the uppermost ( 0.2 or Fe geotherms (>60ºC/km) that are characteristic of rifted regions preclude any contribution to LWMA at depths >10 km. Hence, only upper basalts and hypovolcanic mafic sills would constitute potential magnetic sources. In contrast, the margins of these rifted regions consist of refractory cratonic domains, often characterized by oxidized sublithospheric mantle that host significant concentrations of primary magnetite. The higher NRMs of these peridotites (up to 15 A/m, Qn > 2.5) combined with much lower geotherms (as low as 15ºC/km) allows for a 5 to 10 km layer of uppermost mantle to potentially contribute to LWMA. Assuming that Qn values in rift margins are also gradient across the rift would primarily reflect thermal equilibration over time.

Compositional variations of chromiferous spinel in Mg-rich rocks of ...

Indian Academy of Sciences (India)

tions typical of spinels found in mid-ocean ridge basalts. ... composition of the source region of the magmas ... The Deccan Traps, one of the largest continen- tal LIPs ... outcrops in the Seychelles Islands (Mahoney 1988; ...... Beane J E 1994 A role for lower continental crust in flood ... magmatic evolution; J. Asian Earth Sci.

Metasomatic processes in the orthogneiss-hosted Archaean peridotites of the Fiskefjord region, SW Greenland

Science.gov (United States)

Szilas, K.; Cruz, M. F.; Grove, M.; Morishita, T.; Pearson, D. G.

2016-12-01

Field observations and preliminary geochemical data are presented for large (>500x1000m) peridotite enclaves from the Fiskefjord region of SW Greenland. These ultramafic complexes are dominated by dunite, amphibole-harzburgite, lesser amounts of norite and horizons of stratiform chromitite and are therefore interpreted as cumulate rocks[1]. The ultramafic enclaves are hosted by intrusive tonalitic orthogneiss, which provide U-Pb zircon minimum age constraints of ca. 2980 Ma, whereas preliminary Re-Os isotope data on the dunite and chromitite yield TRD ages of ca. 3300 Ma[2]. Dunite has highly forsteritic olivine compositions with Mg# mostly around 92 to 93, which is uncorrelated with the bulk-rock mg# or modal chromite contents. This indicates that the primary olivine records equilibration with a highly magnesian parental magma, which may have been responsible for the strong depletion of the SCLM in this region. Amphibole and phlogopite is mostly associated with granitoid sheets or infiltrating veins in the dunite and appear to replace chromite. Argon dating (40Ar/39Ar) of the phlogopite yields ages ranging from ca. 3400 Ma to ca. 1750 Ma, with most ages clustering around 3000 Ma. This is consistent with formation of the phlogopite and amphibole by metasomatic processes involving reaction between granitoid-derived siliceous fluids and the ultramafic rocks. The older 40Ar/39Ar age plateaus most plausibly represent excess Ar, potentially inherited from the nearby Itsaq Gneiss Complex (3900 to 3600 Ga) based on its proximity. The youngest 40Ar/39Ar age plateaus on the other hand may potentially signify the closure-age for this system, which could have important implications for determining the exhumation history of the North Atlantic craton. References [1] Szilas, K., Kelemen, P. B., & Bernstein, S. (2015). Peridotite enclaves hosted by Mesoarchaean TTG-suite orthogneisses in the Fiskefjord region of southern West Greenland. GeoResJ, 7, 22-34. [2] Szilas, K., van

Characterization of Organic Materials in the Xenolithic Clasts in Sharps (H3.4) Meteorite Using Micro-Raman Spectroscopy

Science.gov (United States)

Chan, Q. H. S.; Zolensky, M. E.; Bodnar, R. J.; Kebukawa, Y.

2015-01-01

Graphitization of carbon is an irreversible process which alters the structure of graphitic materials in response to the increase in metamorphic grade (temperature and/or pressure). Carbonaceous materials offer a reliable geothermometer as their Raman spectra change systematically with increasing metamorphic grade. In this study, we identified carbonaceous materials in the xenolithic clasts in Sharps and interpreted their metamorphic history by revealing the structural organization (order) of the polyaromatic organic phases using micro-Raman spectroscopy.

Sodium storage capability of spinel Li4Mn5O12

International Nuclear Information System (INIS)

Zhang, Jiaolong; Wang, Wenhui; Li, Yingshun; Yu, Denis Y.W.

2015-01-01

Highlights: • Electrochemical behavior of spinel Li 4 Mn 5 O 12 is examined in Na-ion battery. • A capacity of 120.7 mAh g −1 is obtained during the first sodiation process. • Na storage performance is found to be strongly dependent on particle size. • Ion-exchange between Li ions and Na ions occurs in Li 4 Mn 5 O 12 structure upon cycling. • Loss of crystallinity with cycling, leading to capacity fading. - Abstract: Spinel Li 4 Mn 5 O 12 , a well-known 3 V Li-ion battery (LIB) material with excellent cycling stability and good rate capability, is examined as Na-ion battery (NIB) cathode for the first time. Electrochemical studies clearly show that Na ions can be reversibly inserted into and extracted from the three-dimensional spinel structure. However, unlike in LIB, the available capacity in NIB is strongly dependent on the particle size and current rate due to the sluggish Na-ion transport in solid phase. Cycle performance of Li 4 Mn 5 O 12 in NIB is also inferior to that in LIB. Ex-situ X-ray diffraction study indicates a gradual loss of crystallinity with cycling, and that the crystal lattice undergoes an irreversible expansion during the initial 20 cycles. Inductively coupled plasma spectroscopy shows a decrease of Li/Mn ratio in Li 4 Mn 5 O 12 with cycling. The results suggest that Li ions are removed from the material during the charging process. The charge-discharge mechanism is also discussed in the paper.

Structural, dielectric and gas sensing behavior of Mn substituted spinel MFe2O4 (M=Zn, Cu, Ni, and Co) ferrite nanoparticles

Science.gov (United States)

Ranjith Kumar, E.; Siva Prasada Reddy, P.; Sarala Devi, G.; Sathiyaraj, S.

2016-01-01

Spinel ferrite (MnZnFe2O4, MnCuFe2O4, MnNiFe2O4 and MnCoFe2O4) nanoparticles have been prepared by evaporation method. The annealing temperature plays an important role on changing particle size of the spinel ferrite nanoparticles was found out by X-ray diffraction and transmission electron microscopy. The role of manganese substitution in the spinel ferrite nanoparticles were also analyzed for different annealing temperature. The substitution of Mn also creates a vital change in dielectric properties have been measured in the frequency range of 100 kHz to 5 MHz. These spinel ferrites are decomposed to α-Fe2O3 after annealing above 550 °C in air. Through the characterization of the prepared powder, the effect of annealing temperature, chemical composition and preparation technique on the microstructure, particle size and dielectric properties of the Mn substituted spinel ferrite nanoparticles are discussed. Furthermore, Conductance response of Mn substituted MFe2O4 ferrite nanoparticles were measured by exposing the materials to reducing gas like liquefied petroleum gas (LPG).

Structural and optical high-pressure study of spinel-type MnIn2S4

International Nuclear Information System (INIS)

Manjon, F.J.; Segura, A.; Pellicer-Porres, J.; Sanchez-Royo, J.F.; Amboage, M.; Itie, J.P.; Flank, A.M.; Lagarde, P.; Polian, A.; Ursaki, V.V.; Tiginyanu, I.M.

2007-01-01

We report a combined study of the structural and electronic properties of the spinel-type semiconductor MnIn 2 S 4 under high pressures by means of X-ray diffraction (ADXRD), X-ray absorption (XAS), and optical absorption measurements. The three techniques evidence a reversible structural phase transition near 7 GPa, that according to ADXRD measurements is to a double-NaCl structure. XAS measurements evidence predominant tetrahedral coordination for Mn in the spinel phase that does not noticeably change with increasing pressure up to the phase transition. XAS measurements indicate that the static disorder increases considerably when the sample reverts from the double-NaCl phase to the spinel phase. Optical absorption measurements show that the direct gap of MnIn 2 S 4 exhibits a nonlinear behaviour with a positive pressure coefficient at pressures below 2.5 GPa and a negative pressure coefficient between 2.5 and 7 GPa. The pressure behavior of the bandgap seems to be affected by the defect concentration. The double-NaCl phase also exhibits a bandgap with a negative pressure coefficient. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Black and green pigments based on chromium-cobalt spinels

Energy Technology Data Exchange (ETDEWEB)

Eliziario, Sayonara A., E-mail: sayonaraea@iq.unesp.br [Departamento de Fisico-Quimica, Instituto de Quimica, UNESP - Univ Estadual Paulista, Araraquara, SP (Brazil); Departamento de Quimica, CCEN, Universidade Federal da Paraiba, Campus I, Joao Pessoa, PB (Brazil); Andrade, Jeferson M. de [Departamento de Quimica, CCEN, Universidade Federal da Paraiba, Campus I, Joao Pessoa, PB (Brazil); Lima, Severino J.G. [Departamento de Engenharia Mecanica, CT, Universidade Federal da Paraiba, Campus I, Joao Pessoa, PB (Brazil); Paskocimas, Carlos A. [Universidade Federal do Rio Grande do Norte, CT, Natal, RN (Brazil); Soledade, Luiz E.B. [Departamento de Quimica, CCEN, Universidade Federal da Paraiba, Campus I, Joao Pessoa, PB (Brazil); Hammer, P.; Longo, E. [Departamento de Fisico-Quimica, Instituto de Quimica, UNESP - Univ Estadual Paulista, Araraquara, SP (Brazil); Souza, Antonio G.; Santos, Ieda M.G. [Departamento de Quimica, CCEN, Universidade Federal da Paraiba, Campus I, Joao Pessoa, PB (Brazil)

2011-09-15

Highlights: {yields} Co(Co{sub 2-x}Cr{sub x})O{sub 4} powders with different chromium concentrations (x = 0, 0.25 and 1) were prepared by the polymeric precursor method. {yields} Co(CoCr)O{sub 4} and Co(Co{sub 1.75}Cr{sub 0.25})O{sub 4} displayed a dark color and CoCr{sub 2}O{sub 4} was green. {yields} The colors were related to the different oxidation states of Cr and Co. {yields} Cobalt enrichment result in an increasing presence of Co(III) and a decrease amount of Cr(VI). - Abstract: Chromium and cobalt oxides are widely used in the manufacture of industrial pigments. In this work, the Co(Co{sub 2-x}Cr{sub x})O{sub 4} powders with different chromium concentrations (x = 0, 0.25 and 1) were synthesized by the polymeric precursor method, heat treatment between 600 and 1000 deg. C. These powders were characterized by X-ray diffraction, infrared spectroscopy, colorimetry, UV-vis absorption and X-ray photoelectron spectroscopies. Even with the addition of chromium, the XRD patterns revealed that all powders crystallize in a single spinel cubic structure. The spinels with higher cobalt amount, Co(CoCr)O{sub 4} and Co(Co{sub 1.75}Cr{sub 0.25})O{sub 4}, displayed a dark color, without the Co{sup 3+} reduction observed in Co{sub 3}O{sub 4} between 900 and 950 deg. C. The spinel with higher chromium amount, CoCr{sub 2}O{sub 4}, was green. The colors were directly related to the occupation of tetrahedral and octahedral sites by the chromophores, as well as to the different oxidation states of chromium and cobalt. The different optical band gap values estimated from UV-vis spectra suggested the existence of intermediary energy levels within the band gap. X-ray photoelectron spectroscopy confirmed an increasing presence of Co(III) and a decreasing amount of Cr(VI) with cobalt enrichment.

Nanosized spinel oxide catalysts for CO-oxidation prepared via CoMnMgAl quaternary hydrotalcite route

Energy Technology Data Exchange (ETDEWEB)

Mokhtar, M., E-mail: mmoustafa@kau.edu.s [Chemistry Department, Faculty of Science, King Abdulaziz University, 21589 Jeddah, P.O. Box 80203 (Saudi Arabia); Basahel, S.N.; Al-Angary, Y.O. [Chemistry Department, Faculty of Science, King Abdulaziz University, 21589 Jeddah, P.O. Box 80203 (Saudi Arabia)

2010-03-18

Catalytic activity of the Co-Mn-Mg-Al mixed oxide spinel catalysts was examined in CO oxidation by O{sub 2}. The prepared catalysts were characterized by chemical analysis (ICP), infrared spectroscopy (FTIR), thermal analysis (TG, DTG), powder X-ray diffraction (XRD), surface area measurements, and scanning electron microscopy (SEM).The calcined hydrotalcite-like precursor was composed of spinel-like Co-Mn-Mg-Al mixed oxide as the only XRD crystalline phases. The nanosized spinel oxide catalysts produced by calcination of hydrotalcites showed higher S{sub BET} than CoMn-hydrotalcite samples as calcination led to dehydroxylation and carbonate decomposition of anions in interlayer spaces. All the catalysts showed 100% CO conversion at high temperature even those calcined at 800 {sup o}C. A catalyst with Co/Mn = 4 and calcined at 500 {sup o}C showed 100% CO conversion at 160 {sup o}C. Moreover, this catalyst exhibited quite good durability without deactivation in 60 h stability test.

A mantle origin for Paleoarchean peridotitic diamonds from the Panda kimberlite, Slave Craton: Evidence from 13C-, 15N- and 33,34S-stable isotope systematics

Science.gov (United States)

Cartigny, Pierre; Farquhar, James; Thomassot, Emilie; Harris, Jeffrey W.; Wing, Bozwell; Masterson, Andy; McKeegan, Kevin; Stachel, Thomas

2009-11-01

In order to address diamond formation and origin in the lithospheric mantle underlying the Central Slave Craton, we report N- and C-stable isotopic compositions and N-contents and aggregation states for 85 diamonds of known paragenesis (73 peridotitic, 8 eclogitic and 4 from lower mantle) from the Panda kimberlite (Ekati Mine, Lac de Gras Area, Canada). For 12 peridotitic and two eclogitic sulfide inclusion-bearing diamonds from this sample set, we also report multiple-sulfur isotope ratios. The 73 peridotitic diamonds have a mean δ13C-value of - 5.2‰ and range from - 6.9 to - 3.0‰, with one extreme value at - 14.1‰. The associated δ15N-values range from - 17.0 to + 8.5‰ with a mean value of - 4.0‰. N-contents range from 0 to 1280 ppm. The 8 eclogitic diamonds have δ13C-values ranging from - 11.2 to - 4.4‰ with one extreme value at - 19.4‰. Their δ15N ranges from - 2.1 to + 7.9‰ and N-contents fall between 0 and 3452 ppm. Four diamonds with an inferred lower mantle origin are all Type II (i.e. nitrogen-free) and have a narrow range of δ13C values, between - 4.5 and - 3.5‰. The δ34S of the 14 analyzed peridotitic and eclogitic sulfide inclusions ranges from - 3.5 to +5.7‰. None of them provide evidence for anomalous δ33S-values; observed variations in δ33S are from +0.19 to - 0.33‰, i.e. within the 2 sigma uncertainties of mantle sulfur ( δ33S = 0‰). At Panda, the N contents and the δ13C of sulfide-bearing peridotitic diamonds show narrower ranges than silicate-bearing peridotitic diamonds. This evidence supports the earlier suggestion established from eclogitic diamonds from the Kaapvaal that sulfide-(±silicate) bearing diamonds sample a more restricted portion of sublithospheric mantle than silicate-(no sulfide) bearing diamonds. Our findings at Panda suggest that sulfide-bearing diamonds should be considered as a specific diamond population on a global-scale. Based on our study of δ34S, Δ 33S, δ15N and δ13C, we find no

Synthesis of lithium-manganese-oxide spinels: A study by thermal analysis

CSIR Research Space (South Africa)

Thackeray, MM

1994-12-01

Full Text Available The synthesis of lithium-manganese-oxide spinels by reaction of Li2CO3 and MnCO3 in air and under nitrogen to T(max) = 600°C has been investigated by thermogravimetric analysis and differential scanning calorimetry. When the reaction is conducted...

Chemical compositions and Sr, Nd isotope ratios of gabbroic xenoliths in calc-alkali andesites of Naeba and Torikabuto volcanoes, North Fossa Magna, central Japan

International Nuclear Information System (INIS)

Shimazu, Mitsuo; Kawano, Yoshinobu; Kaji, Kiyoshi; Igarashi, Satoshi.

1991-01-01

Gabbroic, doleritic and basaltic xenoliths found in calc-alkali andesites of Naeba and Torikabuto volcanoes are geochemically divided into three groups. Gabbro A of the group 1 from Naeba is rich in MgO and Ni, poor in alkalis, and shows depleted REE pattern resembling those of Ichinomegata (Sp. No.2232) and Hakone (HKG1, HKG2) volcanoes. On the basis the REE pattern and high Al IV contents in clinopyroxenes, gabbro A is interpreted to have been cumulate from a primary magma generated by partial melting of upper mantle. From REE pattern, gabbros of the group 2 from Ichinomegata (Sp. No.2218) may have derived from low alkali tholeiite magma which have been formed by removal of material such as the group 1 gabbro at shallow depth. Doleritic and basaltic xenoliths of the group 3 from Naeba, gabbroic xenoliths from Torikabuto and Umikawa are poorer in MgO and richer in alkalis than those of the group 1 and show enriched pattern in REE resembling that of high alkali tholeiite and contain clinopyroxenes having low Al IV . Therefore, these rocks are considered to be differentiates of high alkali tholeiite magma at shallow depth. On εNd- 87 Sr/ 86 Sr diagram, isotope data of gabbro A of the group 1 plot near those of andesites from Asama and Myoko volcanoes of the North Fossa Magna. It is interpreted that these rocks have derived from the same mantle source as the Asama and Myoko volcanoes which are richer in incompatible elements than those of MORB. (author)

Preservation of an Archaean whole rock Re-Os isochron for the Venetia lithospheric mantle: Evidence for rapid crustal recycling and lithosphere stabilisation at 3.3 Ga

Science.gov (United States)

van der Meer, Quinten H. A.; Klaver, Martijn; Reisberg, Laurie; Riches, Amy J. V.; Davies, Gareth R.

2017-11-01

Re-Os and platinum group element analyses are reported for peridotite xenoliths from the 533 Ma Venetia kimberlite cluster situated in the Limpopo Mobile Belt, the Neoarchaean collision zone between the Kaapvaal and Zimbabwe Cratons. The Venetian xenoliths provide a rare opportunity to examine the state of the cratonic lithosphere prior to major regional metasomatic disturbance of Re-Os systematics throughout the Phanerozoic. The 32 studied xenoliths record Si-enrichment that is characteristic of the Kaapvaal lithospheric mantle and can be subdivided into five groups based on Re-Os analyses. The most pristine group I samples (n = 13) display an approximately isochronous relationship and fall on a 3.28 ± 0.17 Ga (95 % conf. int.) reference line that is based on their mean TMA age. This age overlaps with the formation age of the Limpopo crust at 3.35-3.28 Ga. The group I samples derive from ∼50 to ∼170 km depth, suggesting coeval melt depletion of the majority of the Venetia lithospheric mantle column. Group II and III samples have elevated Re/Os due to Re addition during kimberlite magmatism. Group II has otherwise undergone a similar evolution as the group I samples with overlapping 187Os/188Os at eruption age: 187Os/188OsEA, while group III samples have low Os concentrations, unradiogenic 187Os/188OsEA and were effectively Re-free prior to kimberlite magmatism. The other sample groups (IV and V) have disturbed Re-Os systematics and provide no reliable age information. A strong positive correlation is recorded between Os and Re concentrations for group I samples, which is extended to groups II and III after correction for kimberlite addition. This positive correlation precludes a single stage melt depletion history and indicates coupled remobilisation of Re and Os. The combination of Re-Os mobility, preservation of the isochronous relationship, correlation of 187Os/188Os with degree of melt depletion and lack of radiogenic Os addition puts tight constraints on

Mg-spinel lithology: A new rock type on the lunar farside

Science.gov (United States)

Pieters, C.M.; Besse, S.; Boardman, J.; Buratti, B.; Cheek, L.; Clark, R.N.; Combe, J.-P.; Dhingra, D.; Goswami, J.N.; Green, R.O.; Head, J.W.; Isaacson, P.; Klima, R.; Kramer, G.; Lundeen, S.; Malaret, E.; McCord, T.; Mustard, J.; Nettles, J.; Petro, N.; Runyon, C.; Staid, M.; Sunshine, J.; Taylor, L.A.; Thaisen, K.; Tompkins, S.; Whitten, J.

2011-01-01

High-resolution compositional data from Moon Mineralogy Mapper (M 3) for the Moscoviense region on the lunar farside reveal three unusual, but distinctive, rock types along the inner basin ring. These are designated "OOS" since they are dominated by high concentrations of orthopyroxene, olivine, and Mg-rich spinel, respectively. The OOS occur as small areas, each a few kilometers in size, that are widely separated within the highly feldspathic setting of the basin rim. Although the abundance of plagioclase is not well constrained within the OOS, the mafic mineral content is exceptionally high, and two of the rock types could approach pyroxenite and harzburgite in composition. The third is a new rock type identified on the Moon that is dominated by Mg-rich spinel with no other mafic minerals detectable (lunar crust; they may thus be near contemporaneous with crustal products from the cooling magma ocean. Copyright ?? 2011 by the American Geophysical Union.

Abnormal lithium isotope composition from the ancient lithospheric mantle beneath the North China Craton.

Science.gov (United States)

Tang, Yan-Jie; Zhang, Hong-Fu; Deloule, Etienne; Su, Ben-Xun; Ying, Ji-Feng; Santosh, M; Xiao, Yan

2014-03-04

Lithium elemental and isotopic compositions of olivines in peridotite xenoliths from Hebi in the North China Craton provide direct evidence for the highly variable δ(7)Li in Archean lithospheric mantle. The δ(7)Li in the cores of olivines from the Hebi high-Mg# peridotites (Fo > 91) show extreme variation from -27 to +21, in marked deviation from the δ(7)Li range of fresh MORB (+1.6 to +5.6) although the Li abundances of the olivines are within the range of normal mantle (1-2 ppm). The Li abundances and δ(7)Li characteristics of the Hebi olivines could not have been produced by recent diffusive-driven isotopic fractionation of Li and therefore the δ(7)Li in the cores of these olivines record the isotopic signature of the subcontinental lithospheric mantle. Our data demonstrate that abnormal δ(7)Li may be preserved in the ancient lithospheric mantle as observed in our study from the central North China Craton, which suggest that the subcontinental lithospheric mantle has experienced modification of fluid/melt derived from recycled oceanic crust.

Power generation using spinel manganese-cobalt oxide as a cathode catalyst for microbial fuel cell applications.

Science.gov (United States)

Mahmoud, Mohamed; Gad-Allah, Tarek A; El-Khatib, K M; El-Gohary, Fatma

2011-11-01

This study focused on the use of spinel manganese-cobalt (Mn-Co) oxide, prepared by a solid state reaction, as a cathode catalyst to replace platinum in microbial fuel cells (MFCs) applications. Spinel Mn-Co oxides, with an Mn/Co atomic ratios of 0.5, 1, and 2, were prepared and examined in an air cathode MFCs which was fed with a molasses-laden synthetic wastewater and operated in batch mode. Among the three Mn-Co oxide cathodes and after 300 h of operation, the Mn-Co oxide catalyst with Mn/Co atomic ratio of 2 (MnCo-2) exhibited the highest power generation 113 mW/m2 at cell potential of 279 mV, which were lower than those for the Pt catalyst (148 mW/m2 and 325 mV, respectively). This study indicated that using spinel Mn-Co oxide to replace platinum as a cathodic catalyst enhances power generation, increases contaminant removal, and substantially reduces the cost of MFCs. Copyright © 2011 Elsevier Ltd. All rights reserved.

The evolution of complex type B Allende inclusion - An ion microprobe trace element study

Science.gov (United States)

Macpherson, Glenn J.; Crozaz, Ghislaine; Lundberg, Laura L.

1989-01-01

Results are presented of a detailed trace-element and isotopic analyses of the constituent phases in each of the major textural parts (mantle, core, and islands) of a Type B refractory inclusion, the USNM 5241 inclusion from Allende, first described by El Goresy et al. (1985). The REE data on 5241 were found to be largely consistent with a model in which the mantle and the core of 5241 formed sequentially out of a single melt by fractional crystallization. The numerical models of REE evolution in the 5241 melt, especially that of Eu, require that a significant mass of spinel-free island material was assimilated into the evolving melt during the last half of the solidification history of 5241. The trace element results pbtained thus strongly support the interpretation of El Goresy et al. (1985) that the spinel-free islands in the 5241 are trapped xenoliths.

Influence of Mn-Co Spinel Coating on Oxidation Behavior of Ferritic SS Alloys for SOFC Interconnect Applications

DEFF Research Database (Denmark)

Venkatachalam, Vinothini; Molin, Sebastian; Kiebach, Wolff-Ragnar

2014-01-01

Chromia forming ferritic stainless steels (SS) are being considered for intermediate temperature solid oxide fuel cell interconnect applications. However, protective coatings are in general needed to avoid chromium volatilization and poisoning of cathodes from chromium species. Mn-Co spinel is one...... of the promising candidates to prevent chromium outward diffusion, improve oxidation resistance and ensure high electrical conductivity over the lifetime of interconnects. In the present study, uniform and well adherent Mn-Co spinel coatings were produced on Crofer 22APU using electrophoretic deposition (EPD...

Effect of gamma irradiation on the structural and magnetic properties of Co–Zn spinel ferrite nanoparticles

International Nuclear Information System (INIS)

Raut, Anil V.; Kurmude, D.V.; Shengule, D.R.; Jadhav, K.M.

2015-01-01

Highlights: • Co–Zn ferrite nanoparticles were examined before and after γ-irradiation. • Single phase cubic spinel structure of Co–Zn was confirmed by XRD data. • The grain size was reported in the range of 52–62 nm after γ-irradiation. • Ms, Hc, n B were reported to be increased after gamma irradiation. - Abstract: In this work, the structural and magnetic properties of Co 1−x Zn x Fe 2 O 4 (0.0 ≤ x ≤ 1.0) ferrite nanoparticles were studied before and after gamma irradiation. The as-synthesized samples of Co–Zn ferrite nanoparticles prepared by sol–gel auto-combustion technique were analysed by XRD which suggested the single phase; cubic spinel structure of the material. Crystal defects produced in the spinel lattice were studied before and after Co 60 γ-irradiation in a gamma cell with a dose rate of 0.1 Mrad/h in order to report the changes in structural and magnetic properties of the Co–Zn ferrite nanoparticles. The average crystallite size (t), lattice parameter (α) and other structural parameters of gamma-irradiated and un-irradiated Co 1−x Zn x Fe 2 O 4 spinel ferrite system was calculated from XRD data. The morphological characterizations were performed using scanning electron microscopy (SEM). The magnetic properties were measured using pulse field hysteresis loop tracer by applying magnetic field of 1000 Oe, and the analysis of data obtained revealed that the magnetic property such as saturation magnetization (Ms), coecivity (Hc), magneton number (n B ) etc. magnetic parameters were increased after irradiation

Mitigation of chromium poisoning of cathodes in solid oxide fuel cells employing CuMn1.8O4 spinel coating on metallic interconnect

Science.gov (United States)

Wang, Ruofan; Sun, Zhihao; Pal, Uday B.; Gopalan, Srikanth; Basu, Soumendra N.

2018-02-01

Chromium poisoning is one of the major reasons for cathode performance degradation in solid oxide fuel cells (SOFCs). To mitigate the effect of Cr-poisoning, a protective coating on the surface of interconnect for suppressing Cr vaporization is necessary. Among the various coating materials, Cu-Mn spinel coating is considered to be a potential candidate due to their good thermal compatibility, high stability and good electronic conductivity at high temperature. In this study, Crofer 22 H meshes with no protective coating, those with commercial CuMn2O4 spinel coating and the ones with lab-developed CuMn1.8O4 spinel coating were investigated. The lab-developed CuMn1.8O4 spinel coating were deposited on Crofer 22 H mesh by electrophoretic deposition and densified by a reduction and re-oxidation process. With these different Crofer 22 H meshes (bare, CuMn2O4-coated, and CuMn1.8O4-coated), anode-supported SOFCs with Sr-doped LaMnO3-based cathode were electrochemically tested at 800 °C for total durations of up to 288 h. Comparing the mitigating effects of the two types of Cu-Mn spinel coatings on Cr-poisoning, it was found that the performance of the denser lab-developed CuMn1.8O4 spinel coating was distinctly better, showing no degradation in the cell electrochemical performance and significantly less Cr deposition near the cathode/electrolyte interface after the test.

Characterizing and quantifying superparamagnetic magnetite particles in serpentinized mantle peridotite observed in continental ophiolite complexes.

Science.gov (United States)

Ortiz, E.; Vento, N. F. R.; Tominaga, M.; Beinlich, A.; Einsle, J. F.; Buisman, I.; Ringe, E.; Schrenk, M. O.; Cardace, D.

2017-12-01

Serpentinization of mantle peridotite has been recognized as one of the most important energy factories for the deep biosphere. To better evaluate the habitability of the deep biosphere, it is crucial to understand the link between in situ peridotite serpentinization processes and associated magnetite and hydrogen production. Previous efforts in correlating magnetite and hydrogen production during serpentinization processes are based primarily on laboratory experiments and numerical modeling, being challenged to include the contribution of superparamagnetic-sized magnetites (i.e., extremely fine-grained magnetite, petrographically observed as a "pepper flake" like texture in many natural serpentinized rock samples). To better estimate the abundance of superparamagnetic grains, we conducted frequency-dependent susceptibility magnetic measurements at the Institute of Rock Magnetism on naturally serpentinized rock samples from the Coast Range Ophiolite Microbial Observatory (CROMO) in California, USA and the Atlin Ophiolite (British Columbia). In addition, we conducted multiscale EDS phase mapping, BackScattered Electron (BSE) scanning, FIB-nanotomography and STEM-EELS to identify and quantify the superparamagnetic minerals that contribute to the measured magnetic susceptibility signals in our rock samples. Utilizing a multidisciplinary approach, we aim to improve the estimation of hydrogen production based on the abundance of magnetite, that includes the contribution of superparamagnetic particle size magnetite, to ultimately provide a more accurate estimation of bulk deep-biomass hosted by in situ serpentinization processes.

Expansion during the formation of the magnesium aluminate spinel (MgAl(2)O(4)) from its basic oxide (MgO and Al(2)O(3)) powders

Science.gov (United States)

Duncan, Flavia Cunha

The extraordinary expansion during the reaction sintering of the magnesium aluminate spinel (MgAl2O4) from its basic oxide (MgO and Al2O3) powders was studied. Experimental series of different size fractions of the reacting materials were formulated to produce the Mg-Al spinel. After batches were prepared, specimens were compacted and fired in air from 1200° to 1700°C for a fixed firing time. A separate set of specimens was fired as a function of time to determine the reaction kinetic parameters. Dimensional changes confirmed that extraordinary expansions of three to four times greater than the prediction from the reaction of solids occur. The solid-state reactions were monitored by X-ray diffraction. The activation energy of the spinel reaction formation was determined to be 280 +/- 20 kJ/mol. It is believed to be associated with the diffusivity of Mg 2+ in either magnesia or spinel during the development of the final spinel structure. New porosity developed in the compacts during the reaction formation of spinel. Scanning electron microscopy confirmed that the magnesia evaporated leaving behind porous magnesia grains, condensed on the alumina particles and reacted to form a shell of spinel. Hollow spinel particles resulted from the original particles of alumina. These porosities generated within the reacting materials influenced the expansions. Final volumetric expansion could potentially reach 56% as a result of the reaction of solids and the porosity generation within MgO and Al2O3. Models of a single alumina particle with and without development of internal porosity were developed. 3-D arrangements of particles showed additional porosity, influencing on the expansions. The decrease in porosity of some specimens fired at higher temperatures indicated that sintering and densification occur simultaneously with the reaction formation of spinel. The decrease in the interparticle porosity limits the full expansion of the particulates to levels lower than the

On the Utility of Spinel Oxide Hosts for Magnesium-Ion Batteries.

Science.gov (United States)

Knight, James C; Therese, Soosairaj; Manthiram, Arumugam

2015-10-21

There is immense interest to develop Mg-ion batteries, but finding suitable cathode materials has been a challenge. The spinel structure has many advantages for ion insertion and has been successfully used in Li-ion batteries. We present here findings on the attempts to extract Mg from MgMn2O4-based spinels with acid (H2SO4) and with NO2BF4. The acid treatment was able to fully remove all Mg from MgMn2O4 by following a mechanism involving the disproportionation of Mn(3+), and the extraction rate decreased with increasing cation disorder. Samples with additional Mg(2+) ions in the octahedral sites (e.g., Mg1.1Mn1.9O4 and Mg1.5Mn1.5O4) also exhibit complete or near complete demagnesiation due to an additional mechanism involving ion exchange of Mg(2+) by H(+), but no Mg could be extracted from MgMnAlO4 due to the disruption of Mn-Mn interaction/contact across shared octahedral edges. In contrast, no Mg could be extracted with the oxidizing agent NO2BF4 from MgMn2O4 or Mg1.5Mn1.5O4 as the electrostatic repulsion between the divalent Mg(2+) ions prevents Mg(2+) diffusion through the 16c octahedral sites, unlike Li(+) diffusion, suggesting that spinels may not serve as potential hosts for Mg-ion batteries. The ability to extract Mg with acid in contrast to that with NO2BF4 is attributed to Mn dissolution from the lattice and the consequent reduction in electrostatic repulsion. The findings could provide insights toward the design of Mg hosts for Mg-ion batteries.

Thermoluminescence of Stoichiometric Magnesium-Aluminium Spinel Defects

International Nuclear Information System (INIS)

Kobyakov, V.A.; Gritsina, V.T.; Kazarinov, Yu.G.; Volokitin, V.N.

2005-01-01

The investigations of thermoluminescence of spinel single crystals MgAl 2 O 4 after UV- and X-ray irradiation was provided by using method of self consisting heating. It was shown, that observed maxima at temperatures of ∼360 and ∼530 K in UV- and green ranges of spectra, respectively, are complex and consist of several strongly overlapping partial maxima. By using method of self consisting heating we have revealed the approximate position of partial maxima, which are included in maxima of ∼360 and ∼530 K, and for some partial maxima there was obtained the order of kinetics, activation energies, and frequency factors

Unique atom hyper-kagome order in Na4Ir3O8 and in low-symmetry spinel modifications.

Science.gov (United States)

Talanov, V M; Shirokov, V B; Talanov, M V

2015-05-01

Group-theoretical and thermodynamic methods of the Landau theory of phase transitions are used to investigate the hyper-kagome atomic order in structures of ordered spinels and a spinel-like Na4Ir3O8 crystal. The formation of an atom hyper-kagome sublattice in Na4Ir3O8 is described theoretically on the basis of the archetype (hypothetical parent structure/phase) concept. The archetype structure of Na4Ir3O8 has a spinel-like structure (space group Fd\\bar 3m) and composition [Na1/2Ir3/2](16d)[Na3/2](16c)O(32e)4. The critical order parameter which induces hypothetical phase transition has been stated. It is shown that the derived structure of Na4Ir3O8 is formed as a result of the displacements of Na, Ir and O atoms, and ordering of Na, Ir and O atoms, ordering dxy, dxz, dyz orbitals as well. Ordering of all atoms takes place according to the type 1:3. Ir and Na atoms form an intriguing atom order: a network of corner-shared Ir triangles called a hyper-kagome lattice. The Ir atoms form nanoclusters which are named decagons. The existence of hyper-kagome lattices in six types of ordered spinel structures is predicted theoretically. The structure mechanisms of the formation of the predicted hyper-kagome atom order in some ordered spinel phases are established. For a number of cases typical diagrams of possible crystal phase states are built in the framework of the Landau theory of phase transitions. Thermodynamical conditions of hyper-kagome order formation are discussed by means of these diagrams. The proposed theory is in accordance with experimental data.

Synthesis of inverse ringwoodite sheds light on the subduction history of Tibetan ophiolites.

Science.gov (United States)

Bindi, Luca; Griffin, William L; Panero, Wendy R; Sirotkina, Ekaterina; Bobrov, Andrey; Irifune, Tetsuo

2018-04-03

Tibetan ophiolites are shallow mantle material and crustal slabs that were subducted as deep as the mantle transition zone, a conclusion supported by the discovery of high-pressure phases like inverse ringwoodite in these sequences. Ringwoodite, Mg 2 SiO 4 , exhibits the normal spinel structure, with Mg in the octahedral A site and Si in the tetrahedral B site. Through A and B site-disorder, the inverse spinel has four-coordinated A cations and the six-coordinated site hosts a mixture of A and B cations. This process affects the density and impedance contrasts across the boundaries in the transition zone and seismic-wave velocities in this portion of the Earth. We report the first synthesis at high pressure (20 GPa) and high temperature (1600 °C) of a Cr-bearing ringwoodite with a completely inverse-spinel structure. Chemical, structural, and computational analysis confirm the stability of inverse ringwoodite and add further constraints to the subduction history of the Luobusa peridotite of the Tibetan ophiolites.

Low dielectric loss in nano-Li-ferrite spinels prepared by sol–gel ...

Indian Academy of Sciences (India)

... Refresher Courses · Symposia · Live Streaming. Home; Journals; Bulletin of Materials Science; Volume 39; Issue 1. Low dielectric loss in nano-Li-ferrite spinels prepared by sol–gel auto-combustion technique. Mamata Maisnam Nandeibam Nilima Maisnam Victory Sumitra Phanjoubam. Volume 39 Issue 1 February 2016 ...

Ferromagnetic-phase transition in the spinel-type CuCr2Te4

International Nuclear Information System (INIS)

Suzuyama, Takeshi; Awaka, Junji; Yamamoto, Hiroki; Ebisu, Shuji; Ito, Masakazu; Suzuki, Takashi; Nakama, Takao; Yagasaki, Katsuma; Nagata, Shoichi

2006-01-01

Ferromagnetic-phase transition in spinel-type CuCr 2 Te 4 has been clearly observed. CuCr 2 Te 4 is a telluride-spinel with the lattice constant a=11.134A, which has been synthesized successfully. The heat capacity exhibits a sharp peak due to the ferromagnetic-phase transition with the Curie temperature T C =326K. This value of T C corresponds exactly to that of the negative peak of dM/dT in low field of 1.0Oe. The magnetic susceptibility shows the Curie-Weiss behavior between 380 and 650K with the effective magnetic moment μ eff =4.14μ B /Cr-ion and the Weiss constant θ=+357K. The low temperature magnetization indicates the spin-wave excitations, where the existence of first term of Bloch T 3/2 law and the next T 5/2 term are verified experimentally. This spin-wave excitation is detected up to approximately 250K which is a fairly high temperature

Oceanic mantle rocks reveal evidence for an ancient, 1.2-1.3 Ga global melting event

Science.gov (United States)

Dijkstra, A. H.; Sergeev, D.; McTaminey, L.; Dale, C. W.; Meisel, T. C.

2011-12-01

It is now increasingly being recognized that many oceanic peridotites are refertilized harzburgites, and that the refertilization often masks an extremely refractory character of the original mantle rock 'protolith'. Oceanic peridotites are, when the effects of melt refertilization are undone, often too refractory to be simple mantle melting residues after the extraction of mid-ocean ridge basalts at a spreading center. Rhenium-osmium isotope analysis is a powerful method to look through the effects of refertilization and to obtain constraints on the age of the melting that produced the refractory mantle protolith. Rhenium-depletion model ages of such anomalously refractory oceanic mantle rocks - found as abyssal peridotites or as mantle xenoliths on ocean islands - are typically >1 Ga, i.e., much older than the ridge system at which they were emplaced. In my contribution I will show results from two case studies of refertilized anciently depleted mantle rocks (Macquarie Island 'abyssal' peridotites and Lanzarote mantle xenoliths). Interestingly, very refractory oceanic mantle rocks from sites all around the world show recurring evidence for a Mesoproterozoic (~1.2-1.3 Ga) melting event [1]. Therefore, oceanic mantle rocks seem to preserve evidence for ancient melting events of global significance. Alternatively, such mantle rocks may be samples of rafts of ancient continental lithospheric mantle. Laser-ablation osmium isotope 'dating' of large populations of individual osmium-bearing alloys from mantle rocks is the key to better constrain the nature and significance of these ancient depletion events. Osmium-bearing alloys form when mantle rocks are melted to high-degrees. We have now extracted over >250 detrital osmium alloys from placer gold occurrences in the river Rhine. These alloys are derived from outcrops of ophiolitic mantle rocks in the Alps, which include blocks of mantle rocks emplaced within the Tethys Ocean, and ultramafic lenses of unknown

Electrochemical and spectroscopic characterization of lithium titanate spinel Li{sub 4}Ti{sub 5}O{sub 12}

Energy Technology Data Exchange (ETDEWEB)

Schneider, Holger; Maire, Pascal [Paul Scherrer Institut, Electrochemistry Laboratory, Section Electrochemical Energy Storage, CH-5232 Villigen PSI (Switzerland); Novak, Petr, E-mail: petr.novak@psi.ch [Paul Scherrer Institut, Electrochemistry Laboratory, Section Electrochemical Energy Storage, CH-5232 Villigen PSI (Switzerland)

2011-10-30

Herein we describe electrochemical and spectroscopic properties of lithium titanate spinel as well as an easy method based on colorimetry to determine the lithium content of electrodes containing lithium titanate spinel as active material. Raman microspectrometry measurements have been performed to follow lithium insertion into and extraction from the active material, respectively. The Raman signals display a pronounced fading of intensity already at low levels of lithium intercalation and disappear at a SOC higher than {approx}10%. However, the colorimetric method can be used up to a SOC of 50%.

Mechanical characterization of magnesium aluminate MgO·nAl2O3 spinel single crystals irradiated with Cu- ions

International Nuclear Information System (INIS)

Ohmura, Takahito; Lee, Chi-Gyu; Kishimoto, Naoki

2003-01-01

Ion-irradiation response of spinel single crystals was investigated using a nanoindentation technique. Specimens of stoichiometric (n=1) and non-stoichiometric (n=2.4) single crystals of MgO n(Al 2 O 3 ) spinel were irradiated with 60 keV Cu - ion at room temperature. Dose rate ranged from 1 to 100 μA/cm 2 , and a total dose was kept constant at 3x10 16 ions/cm 2 . Both plastic hardness and elastic modulus of all the irradiated specimens were softened. Radiation-induced swelling simultaneously occurred. Rutherford back scattering spectroscopy detected disordering of spinel crystalline structure. Accordingly, the radiation-induced softening and swelling are ascribed to accumulation of point defects associated with the disordering. In comparison between the stoichiometric and the non-stoichiometric specimens, the radiation-induced softening is suppressed in the non-stoichiometric composition. (author)

Observation and manipulation of magnetic domains in sol gel derived thin films of spinel ferrites

Science.gov (United States)

Datar, Ashwini A.; Mathe, Vikas L.

2017-12-01

Thin films of spinel ferrites, namely zinc substituted nickel, cobalt ferrite, and manganese substituted cobalt ferrite, were synthesized using sol-gel derived spin-coating techniques. The films were characterized using x-ray diffraction, field emission scanning electron microscopy, Fourier transform infrared spectroscopy and Raman spectroscopy techniques for the analysis of structural, morphological and vibrational band transition properties, which confirm the spinel phase formation of the films. The magnetic force microscopy (MFM) technique was used to observe the magnetic domain structure present in the synthesized films. Further, the films were subjected to an external DC magnetic field of 2 kG to orient the magnetic domains and analyzed using an ex situ MFM technique.

The bulk modulus of cubic spinel selenides: an experimental and theoretical study

DEFF Research Database (Denmark)

Waskowska, A.; Gerward, Leif; Olsen, J.S.

2009-01-01

It is argued that mainly the selenium sublattice determines the overall compressibility of the cubic spinel selenides, AB2Se4, and that the bulk modulus for these compounds is about 100GPa. The hypothesis is supported by experiments using high-pressure X-ray diffraction and synchrotron radiation...

The Effect of Composition on Spinel Crystals Equilibrium in Low-Silica High-Level Waste Glasses

International Nuclear Information System (INIS)

Jiricka, Milos; Hrma, Pavel R.; Vienna, John D.

2003-01-01

The liquidus temperature (TL) and the equilibrium mass fraction of spinel were measured in the regions of low-silica (less than 42 mass% SiO2) high-level waste borosilicate glasses within the spinel primary phase field as functions of glass composition. The components that varied, one at a time, were Al2O3, B2O3, Cr2O3, Fe2O3, Li2O, MnO, Na2O, NiO, SiO2, and ZrO2. The effects of Al2O3, B2O3, Fe2O3, NiO, SiO2, and ZrO2 on the TL in this region and in glasses with 42 to 56 mass% SiO2 were similar. However, in the low-silica region, Cr2O3 increased the TL substantially less, and Li2O and Na2O decreased the TL significantly less than in the region with 42 to 56 mass% SiO2. The effect of MnO on the TL of the higher SiO2 glasses is not yet understood with sufficient accuracy. The temperature at which the equilibrium mass fraction of spinel was 1 mass% was 25C to 64C below the TL

The role of praseodymium substituted ions on electrical and magnetic properties of Mg spinel ferrites

Energy Technology Data Exchange (ETDEWEB)

Farid, Muhammad Tahir, E-mail: tahirfaridbzu@gmail.com; Ahmad, Ishtiaq; Kanwal, Muddassara; Murtaza, Ghulam; Ali, Irshad; Khan, Sajjad Ahmad

2017-04-15

Spinel ferrites with composition MgPr{sub y}Fe{sub 2−y}O{sub 4} (y=0.0, 0.025, 0.05, 0.075, 0.10) were successfully synthesized using sol-gel auto-combustion technique. The structural prisoperties of a prepared sintered powder were characterized with the help of X-ray Diffraction (XRD) and then also by using Scanning electron microscopy (SEM). Electrical measurements demonstrate that resistivity and activation energy increases with the Praseodymium substitution while dc resistivity decreases with the rise of temperature showing the semiconductor nature of the synthesized ferrites. Remanence and the saturation magnetization (M{sub s}) decrease while coercivity (H{sub c}) also increases with the increase in praseodymium contents. Anisotropic constant is observed to exhibit similar behavior as H{sub C}. The above mentioned parameters suggest that the synthesized samples are favorable for microwave absorbing purposes. - Highlights: • Magnesium based spinel ferrites were successfully synthesized by sol-gel method. • The spinel phase has been observed in all samples. • The dc resistivity are found to increase with increasing Pr content • The samples with high resistivity have high values of activation energy. • The Ms Decreases with increasing Pr contents while Hc increases.

Inverse spinel transition metal oxides for lithium-ion storage with different discharge/charge conversion mechanisms

International Nuclear Information System (INIS)

Wang, Jiawei; Ren, Yurong; Huang, Xiaobing; Ding, Jianning

2016-01-01

Highlights: • Inverse spinel structure relieves the irreversible phase transition of electrodes. • Anodes with the same structure show different discharge/charge conversion mechanisms. • High reversible capacity confirms the potential feasibility of composites. - Abstract: Inverse spinel transition metal oxides (Fe 3 O 4 , MnFe 2 O 4 , Fe 3 O 4 /reduced graphene oxide and MnFe 2 O 4 /reduced graphene oxide) are prepared by a facile ethylene-glycol-assisted hydrothermal method. The stability of inverse spinel structure and the high specific surface area of nanoscale provide transition metal oxides with high specific capacity. And the surface modification with reduced graphene oxide improves the poor conductivity of pristine transition metal oxides. Pristine Fe 3 O 4 and MnFe 2 O 4 deliver the high initial discharge capacity of 1137.1 and 1088.9 mAh g −1 , respectively. Fe 3 O 4 /reduced graphene oxide and MnFe 2 O 4 /reduced graphene oxide get the reversible capacity of 645.8 and 720 mAh g −1 , respectively, even after 55 cycles. The different discharge/charge conversion mechanisms make them different capacity stability. The great electrochemical performances of composites offer electrodes with suitable characteristics for high-performance energy storage application.

Effect of gamma irradiation on the structural and magnetic properties of Co–Zn spinel ferrite nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Raut, Anil V., E-mail: nano9993@gmail.com [Vivekanand Arts, Sardar Dalipsingh Commerce and Science College, Aurangabad 431004, (M.S.) India (India); Kurmude, D.V. [Milind College of Science, Aurangabad 431004, (M.S.) India (India); Shengule, D.R. [Vivekanand Arts, Sardar Dalipsingh Commerce and Science College, Aurangabad 431004, (M.S.) India (India); Jadhav, K.M. [Department of Physics, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad 431004, (M.S.) India (India)

2015-03-15

Highlights: • Co–Zn ferrite nanoparticles were examined before and after γ-irradiation. • Single phase cubic spinel structure of Co–Zn was confirmed by XRD data. • The grain size was reported in the range of 52–62 nm after γ-irradiation. • Ms, Hc, n{sub B} were reported to be increased after gamma irradiation. - Abstract: In this work, the structural and magnetic properties of Co{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4} (0.0 ≤ x ≤ 1.0) ferrite nanoparticles were studied before and after gamma irradiation. The as-synthesized samples of Co–Zn ferrite nanoparticles prepared by sol–gel auto-combustion technique were analysed by XRD which suggested the single phase; cubic spinel structure of the material. Crystal defects produced in the spinel lattice were studied before and after Co{sup 60} γ-irradiation in a gamma cell with a dose rate of 0.1 Mrad/h in order to report the changes in structural and magnetic properties of the Co–Zn ferrite nanoparticles. The average crystallite size (t), lattice parameter (α) and other structural parameters of gamma-irradiated and un-irradiated Co{sub 1−x}Zn{sub x}Fe{sub 2}O{sub 4} spinel ferrite system was calculated from XRD data. The morphological characterizations were performed using scanning electron microscopy (SEM). The magnetic properties were measured using pulse field hysteresis loop tracer by applying magnetic field of 1000 Oe, and the analysis of data obtained revealed that the magnetic property such as saturation magnetization (Ms), coecivity (Hc), magneton number (n{sub B}) etc. magnetic parameters were increased after irradiation.

Thermodynamic Modelling of Fe-Cr-Ni-Spinel Formation at the Light-Water Reactor Conditions

International Nuclear Information System (INIS)

Kurepin, V. A.; Kulik, D. A.; Hitpold, A.; Nicolet, M.

2002-03-01

In the light water reactors (LWR), the neutron activation and transport of corrosion products is of concern in the context of minimizing the radiation doses received by the personnel during maintenance works. A practically useful model for transport and deposition of the stainless steel corrosion products in LWR can only be based on an improved understanding of chemical processes, in particular, on the attainment of equilibrium in this hydrothermal system, which can be described by means of a thermodynamic solid-solution -aqueous-solution (SSAS) model. In this contribution, a new thermodynamic model for a Fe-Cr-Ni multi-component spinel solid solutions was developed that considers thermodynamic consequences of cation interactions in both spinel sub-Iattices. The obtained standard thermodynamic properties of two ferrite and two chromite end-members and their mixing parameters at 90 bar pressure and 290 *c temperature predict a large miscibility gap between (Fe,Ni) chromite and (Fe,Ni) ferrite phases. Together with the SUPCRT92-98 thermo- dynamic database for aqueous species, the 'spinel' thermodynamic dataset was applied to modeling oxidation of austenitic stainless steel in hydrothermal water at 290*C and 90 bar using the Gibbs energy minimization (GEM) algorithm, implemented in the GEMS-PSI code. Firstly, the equilibrium compositions of steel oxidation products were modelIed as function of oxygen fugacity .fO 2 by incremental additions of O 2 in H 2 O-free system Cr-Fe- Ni-O. Secondly, oxidation of corrosion products in the Fe-Cr-Ni-O-H aquatic system was modelIed at different initial solid/water ratios. It is demonstrated that in the transition region from hydrogen regime to oxygen regime, the most significant changes in composition of two spinel-oxide phases (chromite and ferrite) and hematite must take place. Under more reduced conditions, the Fe-rich ferrite (magnetite) and Ni-poor chromite phases co-exist at equilibrium with a metal Ni phase, maintaining

Thermodynamic Modelling of Fe-Cr-Ni-Spinel Formation at the Light-Water Reactor Conditions

Energy Technology Data Exchange (ETDEWEB)

Kurepin, V.A.; Kulik, D.A.; Hitpold, A.; Nicolet, M

2002-03-01

In the light water reactors (LWR), the neutron activation and transport of corrosion products is of concern in the context of minimizing the radiation doses received by the personnel during maintenance works. A practically useful model for transport and deposition of the stainless steel corrosion products in LWR can only be based on an improved understanding of chemical processes, in particular, on the attainment of equilibrium in this hydrothermal system, which can be described by means of a thermodynamic solid-solution -aqueous-solution (SSAS) model. In this contribution, a new thermodynamic model for a Fe-Cr-Ni multi-component spinel solid solutions was developed that considers thermodynamic consequences of cation interactions in both spinel sub-Iattices. The obtained standard thermodynamic properties of two ferrite and two chromite end-members and their mixing parameters at 90 bar pressure and 290 *c temperature predict a large miscibility gap between (Fe,Ni) chromite and (Fe,Ni) ferrite phases. Together with the SUPCRT92-98 thermo- dynamic database for aqueous species, the 'spinel' thermodynamic dataset was applied to modeling oxidation of austenitic stainless steel in hydrothermal water at 290*C and 90 bar using the Gibbs energy minimization (GEM) algorithm, implemented in the GEMS-PSI code. Firstly, the equilibrium compositions of steel oxidation products were modelIed as function of oxygen fugacity .fO{sub 2} by incremental additions of O{sub 2} in H{sub 2}O-free system Cr-Fe- Ni-O. Secondly, oxidation of corrosion products in the Fe-Cr-Ni-O-H aquatic system was modelIed at different initial solid/water ratios. It is demonstrated that in the transition region from hydrogen regime to oxygen regime, the most significant changes in composition of two spinel-oxide phases (chromite and ferrite) and hematite must take place. Under more reduced conditions, the Fe-rich ferrite (magnetite) and Ni-poor chromite phases co-exist at equilibrium with a metal Ni

Synthesis and structural characteristics of the spinel-type solid solutions in the Mn-V-Fe-O system

International Nuclear Information System (INIS)

Ponomaryov, V.I.; Dubrovina, I.N.; Zakharov, R.G.

1976-01-01

The part of the spinel region bounded by the compounds Mn 3 O 4 , Mn 2 VO 4 , Fe 2 VO 4 , and Fe 3 O 4 in the four-component system Mn-V-Fe-O was studied. The compounds were synthesized by ceramic technology. Samples were heated in a CO 2 atmosphere free of oxygen at 1100 0 C for 25-50 hr. It was found that the average composition of the spinel compound in the system had the formula Mnsub(1.00)Fesub(1.33)Vsub(0.67)O 4 . X-ray and neutron radiogrphic analyses were made. Crystallo-chemical formulas of the solid solutions considered are tabulated. The magnetic moments of saturation, calculated by the Neel model, are shown, and their experimental values are presented. The crystallo-chemical formulas of the spinel solid solutions in the Mn-V-Fe-O system are of interest in interpreting the concentration dependence of the physico-chemical properties of solid solutions of oxides based on metals with varying valence

Preparation of Layered-Spinel Microsphere/Reduced Graphene Oxide Cathode Materials for Ultrafast Charge-Discharge Lithium-Ion Batteries.

Science.gov (United States)

Luo, Dong; Fang, Shaohua; Yang, Li; Hirano, Shin-Ichi

2017-12-22

Although Li-rich layered oxides (LLOs) have the highest capacity of any cathodes used, the rate capability of LLOs falls short of meeting the requirements of electric vehicles and smart grids. Herein, a layered-spinel microsphere/reduced graphene oxide heterostructured cathode (LS@rGO) is prepared in situ. This cathode is composed of a spinel phase, two layered structures, and a small amount of reduced graphene oxide (1.08 wt % of carbon). The assembly delivers a considerable charge capacity (145 mA h g -1 ) at an ultrahigh charge- discharge rate of 60 C (12 A g -1 ). The rate capability of LS@rGO is influenced by the introduced spinel phase and rGO. X-ray absorption and X-ray photoelectron spectroscopy data indicate that Cr ions move from octahedral lattice sites to tetrahedral lattice sites, and that Mn ions do not participate in the oxidation reaction during the initial charge process. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Synthesis and structural characterization of defect spinels in the Lithium-Manganese-Oxide system

CSIR Research Space (South Africa)

Thackeray, MM

1993-10-01

Full Text Available Lithium-manganese-oxides prepared at moderate temperatures are under investigation as insertion electrodes for rechargeable lithium batteries. The structures of two defect-spinel compounds synthesised by the reaction of MnCO3 and Li2CO3 at 400...

Geology and geochemistry of the Redrock Granite and anorthosite xenoliths (Proterozoic in the northern Burro Mountains, Grant County, New Mexico, USA

Directory of Open Access Journals (Sweden)

Virginia T. McLemore

2002-01-01

Full Text Available Mineral ages from the A-type granites and anorthosite xenoliths in the Redrock area in the northwestern Burro Mountains in southwestern New Mexico cluster around ~1220–1225 Ma and provide yet another example of bimodal igneous activity during this time period in the southwestern United States. The metaluminous to peraluminous, marginally alkaline to subalkaline Redrock Granite exhibits the textural, mineralogical, and geochemical features of A-type granitethat was emplaced at a relatively high crustal level. Field relationships, whole rock and mineral geochemical and isotopic trends suggest that the four phases of the Redrock Granite are genetically related, with the miarolitic biotite/alkali feldspar granite being the youngest phase. Spatial relationships and geochemical data suggest that the anorthosite xenoliths were coeval with the RedrockGranite, which is consistent with the anorthosite being derived from the upper mantle, possibly due to deep mantle upwellings, and the Redrock Granite from the lower crust. The process involved melting in the upper mantle, emplacement of anorthosite in the crust resulting in partial crustal melting and thinning, and, finally, intrusion of shallow silicic plutons, the Redrock Granite. The Redrock Granite and anorthosite were presumably derived from sources characterized by subtle, long-term LREE depletion, with εNd (at 1220 Ma values on theorder of +1 to +2.

Petrogenesis of granitoids and associated xenoliths in the early Paleozoic Baoxu and Enping plutons, South China: Implications for the evolution of the Wuyi-Yunkai intracontinental orogen

Science.gov (United States)

Yu, Yang; Huang, Xiao-Long; Sun, Min; He, Peng-Li

2018-05-01

The early Paleozoic Wuyi-Yunkai orogen was associated with extensive felsic magmatic activities and the orogenic core was mainly distributed in the Yunkai and Wugong domains located in the western Cathaysia block and in the Wuyi domain located in the central part of the Cathaysia block. In order to investigate the evolution of the Wuyi-Yunkai orogen, elemental and Sr-Nd isotopic analyses were performed for granites from the Baoxu pluton in the Yunkai domain and from the Enping pluton in the central part of the Cathaysia block. The Baoxu pluton consists of biotite granite with abundant xenoliths of gneissic granite, granodiorite and diorite, and the Enping pluton is mainly composed of massive granodiorite. Biotite granites (441 ± 5 Ma) and gneissic granite xenolith (443 ± 4 Ma) of the Baoxu pluton are all weakly peraluminous (A/CNK = 1.05-1.10). They show high Sr/Y and La/Yb ratios and have negative bulk-rock εNd(t) values (-7.0 to -4.4), which are similar to coeval gneissic S-type granites in the Yunkai domain and were probably derived from dehydration melting of a sedimentary source with garnet residue in the source. Granodiorites (429 ± 3 Ma) from Enping and granodiorite xenolith (442 ± 4 Ma) from Baoxu are metaluminous and have REE patterns with enriched light REE and flat middle to heavy REE, possibly generated by the dehydration melting of an igneous basement at middle to lower crustal level. Diorite xenolith from Baoxu is ultrapotassic (K2O = 4.9 wt%), has high contents of MgO (7.0 wt%), Cr (379 ppm) and Ni (171 ppm) and shows pronounced negative Nb, Ta and Ti anomalies. This xenolith also has negative εNd(t) value (-3.6) and low Rb/Ba and high Ba/Sr ratios, and is thus interpreted to be derived from an enriched lithospheric mantle with the breakdown of phlogopite. Early Paleozoic I- and S-type granites in the Wuyi-Yunkai orogen mostly have negative εNd(t) values and do not have juvenile components, consistent with genesis by an intracontinental

Ferrimagnetism and spin excitation in a Ni–Mn partially inverted spinel prepared using a modified polymeric precursor method

Energy Technology Data Exchange (ETDEWEB)

Ferreira, Rafael A. [Programa de Pos-Graduação em Ciência e Tecnologia de Materiais (POSMAT), Universidade Estadual Paulista, Faculdade de Ciências, Caixa Postal 473, 17033-360 Bauru, São Paulo (Brazil); Institut des Sciences Chimiques de Rennes – UMR 6226, Université de Rennes 1, F-35042 Rennes (France); Tedesco, Julio C.G.; Birk, Jonas O. [The Niels Bohr Institute, University of Copenhagen, DK-2100 Copenhagen (Denmark); Kalceff, Walter, E-mail: wkalceff@uts.edu.au [School of Physics and Advanced Materials, University of Technology Sydney (UTS), P.O. Box 123, Broadway, NSW 2007 (Australia); Yokaichiya, Fabiano [Laboratório Nacional de Luz Síncrotron (LNLS), Caixa Postal 6192, CEP 13083-970 Campinas, São Paulo (Brazil); Comissao Nacional de Energia Nuclear (CNEN), Instituto de Pesquisas Energeticas e Nucleares (IPEN), Reactor Multiproposito Brasileiro - RMB, Avenida Lineo Prestes 2242, Bloco A, Cidade Universitaria Armando Salles de Oliveira, Sao Paulo (Brazil); Rasmussen, Nina [The Niels Bohr Institute, University of Copenhagen, DK-2100 Copenhagen (Denmark); Peña, Octavio [Institut des Sciences Chimiques de Rennes – UMR 6226, Université de Rennes 1, F-35042 Rennes (France); Henry, Paul F. [European Spallation Source ESS AB, Box 176, 22100 Lund (Sweden); Simeoni, Giovanna G. [Heinz Maier-Leibnitz Zentrum (MLZ) and Physics Department, Technische Universität München, Lichtenbergstr. 1, 85748 Garching (Germany); Bordallo, Heloisa N. [The Niels Bohr Institute, University of Copenhagen, DK-2100 Copenhagen (Denmark); European Spallation Source ESS AB, Box 176, 22100 Lund (Sweden); and others

2014-07-01

We demonstrate that a Ni–Mn oxide partially inverted spinel (Ni{sub 1−ν}Mn{sub ν})[Ni{sub ν}Mn{sub 2−ν}]O{sub 4} having inversion degree ν ≈ 0.8 and produced by a modified polymeric precursor method exhibits behaviour previously reported only in monophased samples. The structure of the specimen was determined using Rietveld analysis of X-ray and neutron powder diffraction data, showing that at room temperature the material crystallizes in the Fd3{sup ¯}m space group with a lattice constant a = 8.392 Å. Combining magnetization measurements with neutron powder diffraction, we show that the magnetic structure of this spinel is associated with the interplay between the ferromagnetic and antiferromagnetic lattices which coexist due to the cations' presence on both tetrahedral and octahedral sites. Our analysis of the neutron diffraction data confirms the postulated magnetic structure involving a star-like moment arrangement, arising from competition for the B (octahedral) spinel sites by the Ni and Mn cations. Finally, we show that strong magnetic fluctuations are observed in the inelastic neutron scattering data. - Highlights: • Ni–Mn oxide partially-inverted spinel made by modified polymeric precursor method. • Magnetic measurements showed a ferrimagnetic and a parasitic magnetic transition. • NPD revealed a magnetic structure consistent with a star-like moment arrangement. • INS measurements indicated four distinct temperature-dependent magnetic regimes.

Lithospheric diamond formation as a consequence of methane-rich volatile flooding: An example from diamondiferous eclogite xenoliths of the Karelian craton (Finland)

Science.gov (United States)

Smart, K. A.; Cartigny, P.; Tappe, S.; O'Brien, H.; Klemme, S.

2017-06-01

A collection of 61 xenocrystic and 12 eclogite xenolith-derived diamonds from the 600 Ma Lahtojoki kimberlite in central Finland has been investigated. Calculated pressure and temperature conditions for the diamondiferous eclogites are in excess of 5.5 GPa and 1300 °C, suggesting residence depths greater than 180 km, near the base of the Karelian cratonic mantle lithosphere. Geochemically, the eclogite xenoliths have gabbroic compositions showing positive Eu and Sr anomalies, relatively low ΣREE and elevated Al2O3 contents, yet garnets have ambiguous δ18O values of 5.7‰ and 5.9‰. Gabbroic eclogite formation could therefore be linked to either subduction processes during the 1.9 Ga Svecofennian orogeny or to cumulate processes during 2.1 Ga rift-induced magmatism. Determination of the oxygen fugacity of Lahtojoki eclogite xenoliths from both this work and previous studies suggests that diamond-bearing eclogites may be more reduced (ΔFMQ-3.5) compared to barren eclogites (ΔFMQ-1.7). While recycled oceanic crust protoliths for the eclogites remain a possibility, the carbon isotopic compositions and nitrogen abundances of the Lahtojoki diamonds indicate mantle-derived volatile sources. All diamonds (i.e., loose and eclogite xenolith-derived) display a restricted range of δ13C values from -7.8‰ to -3.7‰ that overlaps with the carbon isotopic composition of Earth's mantle. The Lahtojoki diamond δ13C values form a negatively skewed distribution, indicating diamond growth from reduced mantle-derived carbon sources such as methane- (CH4) bearing fluids. Nitrogen contents of the Lahtojoki diamonds range from 40 to 1830 atomic ppm with a mean of ∼670 atomic ppm; these elevated nitrogen contents combined with the close association to eclogites suggest an eclogitic or crustal volatile source. However, the Karelian craton was periodically intruded by ultramafic alkaline magmas since at least 1.8 Ga, noting in particular the occurrence of phlogopite

Synthesis and structural characterization of defect spinels in the lithium-manganese-oxide system

CSIR Research Space (South Africa)

Thackeray, MM

1993-10-01

Full Text Available Lithium-manganese-oxides prepared at moderate temperatures are under investigation as insertion electrodes for rechargeable lithium batteries. The structures of two defect-spinel compounds synthesized by the reaction of MnCO3 and Li2CO3 at 400°C...

Synthesis of high surface area spinel-type MgAl2O4 nanoparticles by

Indian Academy of Sciences (India)

68

Spinel-type magnesium aluminate, MgAl2O4, is an effective refractory ceramic for ... such as good mechanical strength at high temperatures, high resistance to ... Materials. The starting chemicals with laboratory grade purity were provided ...

Nature of the Electrochemical Properties of Sulphur Substituted LiMn2O4 Spinel Cathode Material Studied by Electrochemical Impedance Spectroscopy

Directory of Open Access Journals (Sweden)

Monika Bakierska

2016-08-01

Full Text Available In this work, nanostructured LiMn2O4 (LMO and LiMn2O3.99S0.01 (LMOS1 spinel cathode materials were comprehensively investigated in terms of electrochemical properties. For this purpose, electrochemical impedance spectroscopy (EIS measurements as a function of state of charge (SOC were conducted on a representative charge and discharge cycle. The changes in the electrochemical performance of the stoichiometric and sulphur-substituted lithium manganese oxide spinels were examined, and suggested explanations for the observed dependencies were given. A strong influence of sulphur introduction into the spinel structure on the chemical stability and electrochemical characteristic was observed. It was demonstrated that the significant improvement in coulombic efficiency and capacity retention of lithium cell with LMOS1 active material arises from a more stable solid electrolyte interphase (SEI layer. Based on EIS studies, the Li ion diffusion coefficients in the cathodes were estimated, and the influence of sulphur on Li+ diffusivity in the spinel structure was established. The obtained results support the assumption that sulphur substitution is an effective way to promote chemical stability and the electrochemical performance of LiMn2O4 cathode material.

Study of Mn dissolution from LiMn{sub 2}O{sub 4} spinel electrodes using rotating ring-disk collection experiments

Energy Technology Data Exchange (ETDEWEB)

Wang, Li-Fang; Ou, Chin-Ching; Striebel, Kathryn A.; Chen, Jenn-Shing

2003-07-01

The goal of this research was to measure Mn dissolution from a thin porous spinel LiMn{sub 2}O{sub 4} electrode by rotating ring-disk collection experiments. The amount of Mn dissolution from the spinel LiMn{sub 2}O{sub 4} electrode under various conditions was detected by potential step chronoamperometry. The concentration of dissolved Mn was found to increase with increasing cycle numbers and elevated temperature. The dissolved Mn was not dependent on disk rotation speed, which indicated that the Mn dissolution from the disk was under reaction control. The in situ monitoring of Mn dissolution from the spinel was carried out under various conditions. The ring currents exhibited maxima corresponding to the end-of-charge (EOC) and end-of-discharge (EOD), with the largest peak at EOC. The results suggest that the dissolution of Mn from spinel LiMn{sub 2}O{sub 4} occurs during charge/discharge cycling, especially in a charged state (at >4.1 V) and in a discharged state (at <3.1 V). The largest peak at EOC demonstrated that Mn dissolution took place mainly at the top of charge. At elevated temperatures, the ring cathodic currents were larger due to the increase of Mn dissolution rate.

Photoelectrochemical and theoretical investigations of spinel type ferrites (MxFe3-xO4) for water splitting: a mini-review

Science.gov (United States)

Taffa, Dereje H.; Dillert, Ralf; Ulpe, Anna C.; Bauerfeind, Katharina C. L.; Bredow, Thomas; Bahnemann, Detlef W.; Wark, Michael

2017-01-01

Solar-assisted water splitting using photoelectrochemical cells (PECs) is one of the promising pathways for the production of hydrogen for renewable energy storage. The nature of the semiconductor material is the primary factor that controls the overall energy conversion efficiency. Finding semiconductor materials with appropriate semiconducting properties (stability, efficient charge separation and transport, abundant, visible light absorption) is still a challenge for developing materials for solar water splitting. Owing to the suitable bandgap for visible light harvesting and the abundance of iron-based oxide semiconductors, they are promising candidates for PECs and have received much research attention. Spinel ferrites are subclasses of iron oxides derived from the classical magnetite (FeIIFe2IIIO4) in which the FeII is replaced by one (some cases two) additional divalent metals. They are generally denoted as MxFe3-xO4 (M=Ca, Mg, Zn, Co, Ni, Mn, and so on) and mostly crystallize in spinel or inverse spinel structures. In this mini review, we present the current state of research in spinel ferrites as photoelectrode materials for PECs application. Strategies to improve energy conversion efficiency (nanostructuring, surface modification, and heterostructuring) will be presented. Furthermore, theoretical findings related to the electronic structure, bandgap, and magnetic properties will be presented and compared with experimental results.

Simple synthetic route to manganese-containing nanowires with the spinel crystal structure

Energy Technology Data Exchange (ETDEWEB)

Yu, Lei; Zhang, Yan; Hudak, Bethany M.; Wallace, Damon K.; Kim, Doo Young; Guiton, Beth S.

2016-08-15

This report describes a new route to synthesize single-crystalline manganese-containing spinel nanowires (NWs) by a two-step hydrothermal and solid-state synthesis. Interestingly, a nanowire or nanorod morphology is maintained during conversion from MnO{sub 2}/MnOOH to CuMn{sub 2}O{sub 4}/Mg{sub 2}MnO{sub 4}, despite the massive structural rearrangement this must involve. Linear sweep voltammetry (LSV) curves of the products give preliminary demonstration that CuMn{sub 2}O{sub 4} NWs are catalytically active towards the oxygen evolution reaction (OER) in alkaline solution, exhibiting five times the magnitude of current density found with pure carbon black. - Highlights: • Synthesis of single-crystalline manganese-containing spinel nanowires. • Binary oxide nanowire converted to ternary oxide wire through solid state reaction. • Approach to structure conversion with shape retention could be generally applicable. • Copper and Manganese display multiple oxidation states with potential for catalysis. • CuMn{sub 2}O{sub 4} nanowires show promise as catalysts for the oxygen evolution reaction.

Synthesis, Characterization, and Sensor Applications of Spinel ZnCo2O4 Nanoparticles

Directory of Open Access Journals (Sweden)

Juan Pablo Morán-Lázaro

2016-12-01

Full Text Available Spinel ZnCo2O4 nanoparticles were synthesized by means of the microwave-assisted colloidal method. A solution containing ethanol, Co-nitrate, Zn-nitrate, and dodecylamine was stirred for 24 h and evaporated by a microwave oven. The resulting solid material was dried at 200 °C and subsequently calcined at 500 °C for 5 h. The samples were characterized by scanning electron microscopy (SEM, transmission electron microscopy (TEM, X-ray diffraction (XRD, and Raman spectroscopy, confirming the formation of spinel ZnCo2O4 nanoparticles with average sizes between 49 and 75 nm. It was found that the average particle size decreased when the dodecylamine concentration increased. Pellets containing ZnCo2O4 nanoparticles were fabricated and tested as sensors in carbon monoxide (CO and propane (C3H8 gases at different concentrations and temperatures. Sensor performance tests revealed an extremely high response to 300 ppm of CO at an operating temperature of 200 °C.

Magnetic and catalytic properties of inverse spinel CuFe{sub 2}O{sub 4} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Anandan, S., E-mail: sanand@nitt.edu [Nanomaterials and Solar Energy Conversion Lab, Department of Chemistry, National Institute of Technology, Trichy 620 015 (India); Department of Environmental Engineering and Science, Feng Chia University, Taichung 407, Taiwan (China); Selvamani, T.; Prasad, G. Guru [Nanomaterials and Solar Energy Conversion Lab, Department of Chemistry, National Institute of Technology, Trichy 620 015 (India); Asiri, A.M. [The Center of Excellence for Advanced Materials Research, King Abdulaziz University, P.O. Box 80203, Jeddah 21413 (Saudi Arabia); Wu, J.J., E-mail: jjwu@fcu.edu.tw [Department of Environmental Engineering and Science, Feng Chia University, Taichung 407, Taiwan (China)

2017-06-15

Highlights: • Copper ferrite (CuFe{sub 2}O{sub 4}) nanoparticles were synthesized via citrate-nitrate combustion method. • Spectroscopic information’s have found that CuFe{sub 2}O{sub 4} nanoparticles as an inverse spinel structure. • Magnetic study exhibits CuFe{sub 2}O{sub 4} nanoparticles have ferromagnetic behavior. • CuFe{sub 2}O{sub 4} nanoparticles employed for photocatalytic decolourisation of methylene blue under visible light irradiation. - Abstract: In this research, inverse spinel copper ferrite nanoparticles (CuFe{sub 2}O{sub 4} NPs) were synthesized via citrate-nitrate combustion method. The crystal structure, particle size, morphology and magnetic studies were investigated using various instrumental tools to illustrate the formation of the inverse spinel structure. Mossbauer spectrometry identified Fe is located both in the tetrahedral and octahedral site in the ratio (40:60) and the observed magnetic parameters values such as saturation magnetization (M{sub s} = 20.62 emu g{sup −1}), remnant magnetization (M{sub r} = 11.66 emu g{sup −1}) and coercivity (H{sub c} = 63.1 mTesla) revealed that the synthesized CuFe{sub 2}O{sub 4} NPs have a typical ferromagnetic behaviour. Also tested CuFe{sub 2}O{sub 4} nanoparticles as a photocatalyst for the decolourisation of methylene blue (MB) in the presence of peroxydisulphate as the oxidant.

An Integrated, Layered-Spinel Composite Cathode for Energy Storage Applications

Science.gov (United States)

Hagh, Nader; Skandan, Ganesh

2012-01-01

At low operating temperatures, commercially available electrode materials for lithium-ion batteries do not fully meet the energy and power requirements for NASA fs exploration activities. The composite cathode under development is projected to provide the required energy and power densities at low temperatures and its usage will considerably reduce the overall volume and weight of the battery pack. The newly developed composite electrode material can provide superior electrochemical performance relative to a commercially available lithium cobalt system. One advantage of using a composite cathode is its higher energy density, which can lead to smaller and lighter battery packs. In the current program, different series of layered-spinel composite materials with at least two different systems in an integrated structure were synthesized, and the volumetric and gravimetric energy densities were evaluated. In an integrated network of a composite electrode, the effect of the combined structures is to enhance the capacity and power capabilities of the material to levels greater than what is possible in current state-of-the-art cathode systems. The main objective of the current program is to implement a novel cathode material that meets NASA fs low temperature energy density requirements. An important feature of the composite cathode is that it has at least two components (e.g., layered and spinel) that are structurally integrated. The layered material by itself is electrochemically inactive; however, upon structural integration with a spinel material, the layered material can be electrochemically activated, thereby delivering a large amount of energy with stable cycling. A key aspect of the innovation has been the development of a scalable process to produce submicronand micron-scale particles of these composite materials. An additional advantage of using such a composite electrode material is its low irreversible loss (.5%), which is primarily due to the unique activation

Alkaline and Carbonate-rich Melt Metasomatism and Melting of Subcontinental Lithospheric Mantle: Evidence from Mantle Xenoliths, NE Bavaria, Bohemian Massif

Czech Academy of Sciences Publication Activity Database

Ackerman, Lukáš; Špaček, Petr; Magna, T.; Ulrych, Jaromír; Svojtka, Martin; Hegner, E.; Balogh, K.

2013-01-01

Roč. 54, č. 12 (2013), s. 2597-2633 ISSN 0022-3530 R&D Projects: GA ČR GA205/09/1170 Institutional research plan: CEZ:AV0Z30130516; CEZ:AV0Z30120515 Institutional support: RVO:67985831 ; RVO:67985530 Keywords : peridotite * metasomatism * subcontinental lithosphere * Sr-Nd-Li isotopes * microstructure Subject RIV: DB - Geology ; Mineralogy Impact factor: 4.485, year: 2013

Synthesis and characterization of inverse spinels, intercalation materials for Li-ion batteries

NARCIS (Netherlands)

Van Landschoot, N.

2006-01-01

Chapter 2 describes the solid-state synthesis of LiNiVO4 and LiCoVO4. The materials are prepared at 800C and are phase pure, as shown by X-ray diffraction and have the inverse spinel structure. Due to the solid-state synthesis the particle size is quite large and the particle size distribution is

CO 2-rich komatiitic melt inclusions in Cr-spinels within beach sand from Gorgona Island, Colombia

Science.gov (United States)

Shimizu, Kenji; Shimizu, Nobumichi; Komiya, Tsuyoshi; Suzuki, Katsuhiko; Maruyama, Shigenori; Tatsumi, Yoshiyuki

2009-10-01

The volatile content of komatiite is a key to constrain the thermal and chemical evolution of the deep Earth. We report the volatile contents with major and trace element compositions of ~ 80 melt inclusions in chromian spinels (Cr-spinels) from beach sands on Gorgona Island, Colombia. Gorgona Island is a ~ 90 Ma volcanic island, where picrites and the youngest komatiites known on the Earth are present. Melt inclusions are classified into three types on the basis of their host Cr-spinel compositions: low Ti (P type), high Ti with high Cr # (K1 type) and high Ti with low Cr # (K2 type). Chemical variations of melt inclusions in the Cr-spinels cover all of the island's lava types. P-type inclusions mainly occur in the picrites, K1-type in high-TiO 2 komatiites (some enriched basalts: E-basalts) and K2-type in low-TiO 2 komatiites. The H 2O and CO 2 contents of melt inclusions within Cr-spinels from the beach sand are highly variable (H 2O: 0.03-0.9 wt.%; CO 2: 40-4000 ppm). Evaluation of volatile content is not entirely successful because of compositional alterations of the original melt by degassing, seawater/brine assimilation and post-entrapment modification of certain elements and volatiles. However, the occurrence of many melt inclusions with low H 2O/K 2O ratios indicates that H 2O/K 2O of Gorgona komatiite is not much different from that of modern mid-oceanic ridge basalt (MORB) or oceanic island basalt. Trend of CO 2/Nb and Zr/Y ratios, accounted for by two-component mixing between the least degassed primary komatiite and low-CO 2/Nb evolved basalt, allow us to estimate a primary CO 2/Nb ratio of 4000 ± 2200 or a CO 2 content of 0.16 ± 0.09 wt.%. The determined CO 2/Nb ratio is unusually high, compared to that of MORB (530). Although the presence of CO 2 in the Gorgona komatiite does not affect the magma generation temperature, CO 2 degassing may have contributed to the eruption of high-density magmas. High CO 2/Nb and the relatively anhydrous nature of

Fertile lithospheric mantle beneath the northwestern North China and its implication for the subduction of the Paleo-Asian Ocean

Science.gov (United States)

Dai, H. K.; Zheng, J.; Su, Y. P.; Xiong, Q.; Pan, S. K.

2017-12-01

The nature of the sub-continental lithospheric mantle (SCLM) beneath the western North China Craton (NCC) is poorly known, which hinders understanding the cratonic response to the southward subduction of the Paleo-Asian Ocean. Mineral chemical data of spinel lherzolite xenoliths from newly discovered Cenozoic Langshan basalts in the northwestern part of the craton have been integrated with data from other localities across the western NCC, to put constrains on the SCLM nature and to explore the reworking processes involved. Compositions of mineral cores (i.e., Mg# in olivine = 88 91) and P-T estimates ( 1.2 GPa, 950 oC) suggest the Langshan xenoliths/xenocrysts represent fragments of the uppermost SCLM and experienced ancient continental crust, and 2) the sharp decrease in lithospheric thickness from the inner part to the northern margin of the western NCC, the SCLM beneath the northwestern part should have been strongly rejuvenated or replaced by fertile and non-cratonic mantle. Combined with other geological evidence on the northwestern margin, the mantle replacement and metasomatism were likely triggered by southward subduction of the Paleo-Asian Ocean.

Intermediate-Depth Subduction Earthquakes Recorded by Pseudotachylyte in Dry Eclogite-Facies Oceanic Lithosphere from the Alps

Science.gov (United States)

Scambelluri, M.; Pennacchioni, G.; Gilio, M.; Bestmann, M.

2016-12-01

While geophysical studies and laboratory experiments provide much information on subduction earthquakes, field studies identifying the rock types for earthquake development and the deep seismogenic environments are still scarce. To date, fluid overpressure and volume decrease during hydrous mineral breakdown the widely favoured trigger of subduction earthquakes in serpentinized lithospheric mantle and hydrated low-velocity layers atop slabs. Here we document up to 40 cm-thick pseudotachylyte (PST) in Alpine oceanic gabbro and peridotite (2-2.5 GPa-550-620°C), the analogue of a modern cold subducting oceanic lithosphere. These rocks mostly remained unaltered dry systems; only very minor domains (<1%) record partial hydration and static eclogitic metamorphism. Meta-peridotite shows high-pressure olivine + antigorite (garnet + zoisite + chlorite after mantle plagioclase); meta-gabbro develops omphacite + zoisite + talc + chloritoid + garnet. Abundant syn-eclogitic pseudotachylyte cut the dry gabbro-peridotite and the eclogitized domains. In meta-peridotite, PST shows olivine, orthopyroxene, spinel microliths and clasts of high-pressure olivine + antigorite and garnet + zoisite + chlorite aggregates. In metagabbro, microfaults in damage zones near PST cut brecciated igneous pyroxene cemented by omphacite. In unaltered gabbro, glassy PST contains micron-scale garnet replacing plagioclase microliths during, or soon after, PST cooling. In the host rock, garnet coronas between igneous olivine and plagioclase only occur near PST and between closely spaced PST veins. Absence of garnet away from PST indicates that garnet growth was triggered by mineral seeds and by heat released by PST. The above evidence shows that pseudotachylyte formed at eclogite-facies conditions. In such setting, strong, dry, metastable gabbro-peridotite concentrate stress to generate large intermediate depth subduction earthquakes without much involvement of free fluid.

Electronic structure and physical properties of the spinel-type phase of BeP2N4 from all-electron density functional calculations

International Nuclear Information System (INIS)

Ching, W. Y.; Aryal, Sitram; Rulis, Paul; Schnick, Wolfgang

2011-01-01

Using density-functional-theory-based ab initio methods, the electronic structure and physical properties of the newly synthesized nitride BeP 2 N 4 with a phenakite-type structure and the predicted high-pressure spinel phase of BeP 2 N 4 are studied in detail. It is shown that both polymorphs are wide band-gap semiconductors with relatively small electron effective masses at the conduction-band minima. The spinel-type phase is more covalently bonded due to the increased number of P-N bonds for P at the octahedral sites. Calculations of mechanical properties indicate that the spinel-type polymorph is a promising superhard material with notably large bulk, shear, and Young's moduli. Also calculated are the Be K, P K, P L 3 , and N K edges of the electron energy-loss near-edge structure for both phases. They show marked differences because of the different local environments of the atoms in the two crystalline polymorphs. These differences will be very useful for the experimental identification of the products of high-pressure syntheses targeting the predicted spinel-type phase of BeP 2 N 4 .

Structure of spinel at high temperature using in-situ XANES study at the Al and Mg K-edge

Energy Technology Data Exchange (ETDEWEB)

Ligny, D de [Universite Claude Bernard Lyon 1, LPCML, 69622 Villeurbanne (France); Neuville, D R [Physique des Mineraux et Magmas, Geochimie-Cosmochimie, CNRS-IPGP, 4 place Jussieu, 75005 Paris (France); Flank, A-M; Lagarde, P, E-mail: deligny@pcml.univ-lyon1.f [Synchrotron SOLEIL, L' Orme des Merisiers, Saint Aubin, 91192 France (France)

2009-11-15

We present structural information obtained on spinel at high temperature (298-2400 K) using in situ XANES at the Mg and Al K-edge. Spinel, {sup [4]}(Al{sub x},Mg{sub 1-x}){sup [6]}(Al{sub 2-x},Mg{sub x})O{sub 4}, with increasing temperature, show a substitution of Mg by Al and Al by Mg in their respective sites. This substitution corresponds to an inversion of the Mg and Al sites. Furthermore, both experiments at the Al and Mg K-edges are in good agreement with XANES calculation made using FDMNES code.

Morphology evolution in spinel manganite films deposited from an aqueous solution

International Nuclear Information System (INIS)

Ko, Song Won; Li, Jing; Trolier-McKinstry, Susan

2012-01-01

Spinel manganite films were deposited by the spin spray technique at low deposition temperatures ( 1000, agglomeration of small particles was dominant, which suggests that homogeneous nucleation is dominant during deposition. Heterogeneous nucleation was critical to obtain dense films. - Highlights: ► Film microstructure depends on supersaturation. ► Heterogeneous nucleation induces dense and continuous films. ► The spin spray technique enables use of a variety of substrates.

Spinel versus layered structures for lithium cobalt oxide synthesized at 400-degrees-c

CSIR Research Space (South Africa)

Gummow, RJ

1993-03-01

Full Text Available -type structure) give comparable fits to the data. This structural anomaly is discussed in terms of the refinements and electrochemical data obtained when lithium is extracted from LiCoO2 in non-aqueous cells at room temperature. A spinel-related model for LixCoO2...

CO2 injection into fractured peridotites: a reactive percolation experiment

Science.gov (United States)

Escario, S.; Godard, M.; Gouze, P.; Leprovost, R.; Luquot, L.; Garcia-Rios, M.

2017-12-01

Mantle peridotites have the potential to trap CO2 as carbonates. This process observed in ophiolites and in oceanic environments provides a long term and safe storage for CO2. It occurs as a part of a complex suite of fluid-rock reactions involving silicate dissolution and precipitation of hydrous phases, carbonates and minor phases that may in turn modify the hydrodynamic properties and the reactivity of the reacted rocks. The efficiency and lastingness of the process require the renewal of fluids at the mineral-fluid interface. Fractures are dominant flow paths in exhumed mantle sections. This study aims at better understanding the effect of CO2-enriched saline fluids on hydrodynamic and chemical processes through fractured peridotites. Experiments were performed using the reactive percolation bench ICARE Lab 3 - Géosciences Montpellier. It allows monitoring the permeability changes during experiments. Effluents are recurrently sampled for analysing cation concentration, pH and alkalinity. Reacted rock samples were characterized by high resolution X-ray microtomography (ESRF ID19, Grenoble, France) and SEM. Experiments consisted in injecting CO2-enriched brines (NaCl 0.5 M) at a rate of 6 mL.h-1 into artificially fractured cores (9 mm diameter × 20 mm length) of Oman harzburgites at T=170°C and Ptotal = 25 MPa for up to 2 weeks. Fractures are of few µm apertures with rough walls. Three sets of experiments were performed at increasing value of [CO2] (0, 0.1 and 1 mol/kg). All experiments showed a decrease in permeability followed by steady state regime that can be caused by a decrease in the roughness of fracture walls (dissolution dominated process), thus favouring fracture closing, or by the precipitation of secondary phases. Maximum enrichments in Mg, Fe and Ca of the effluent fluids occur during the first 2 hours of the experiments whereas Si displays a maximum enrichment at t = 20 h, suggesting extensive dissolution. Maximum enrichments are observed with

Formation of pyroxenite layers in the Totalp ultramafic massif (Swiss Alps) - Insights from highly siderophile elements and Os isotopes

Science.gov (United States)

van Acken, David; Becker, Harry; Walker, Richard J.; McDonough, William F.; Wombacher, Frank; Ash, Richard D.; Piccoli, Phil M.

2010-01-01

Pyroxenitic layers are a minor constituent of ultramafic mantle massifs, but are considered important for basalt generation and mantle refertilization. Mafic spinel websterite and garnet-spinel clinopyroxenite layers within Jurassic ocean floor peridotites from the Totalp ultramafic massif (eastern Swiss Alps) were analyzed for their highly siderophile element (HSE) and Os isotope composition. Aluminum-poor pyroxenites (websterites) display chondritic to suprachondritic initial γOs (160 Ma) of -2 to +27. Osmium, Ir and Ru abundances are depleted in websterites relative to the associated peridotites and to mantle lherzolites worldwide, but relative abundances (Os/Ir, Ru/Ir) are similar. Conversely, Pt/Ir, Pd/Ir and Re/Ir are elevated. Aluminum-rich pyroxenites (clinopyroxenites) are characterized by highly radiogenic 187Os/ 188Os with initial γOs (160 Ma) between +20 and +1700. Their HSE composition is similar to that of basalts, as they are more depleted in Os, Ir and Ru compared to Totalp websterites, along with even higher Pt/Ir, Pd/Ir and Re/Ir. The data are most consistent with multiple episodes of reaction of mafic pyroxenite precursor melts with surrounding peridotites, with the highest degree of interaction recorded in the websterites, which typically occur in direct contact to peridotites. Clinopyroxenites, in contrast, represent melt-dominated systems, which retained the precursor melt characteristics to a large extent. The melts may have been derived from a sublithospheric mantle source with high Pd/Ir, Pt/Ir and Re/Os, coupled with highly radiogenic 187Os/ 188Os compositions. Modeling indicates that partial melting of subducted, old oceanic crust in the asthenosphere could be a possible source for such melts. Pentlandite and godlevskite are identified in both types of pyroxenites as the predominant sulfide minerals and HSE carriers. Heterogeneous HSE abundances within these sulfide grains likely reflect subsolidus processes. In contrast, large grain

Structural, dielectric and gas sensing behavior of Mn substituted spinel MFe{sub 2}O{sub 4} (M=Zn, Cu, Ni, and Co) ferrite nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Ranjith Kumar, E., E-mail: ranjueaswar@gmail.com [Department of Physics, Dr. NGP Institute of Technology, Coimbatore 641048, Tamil Nadu (India); Siva Prasada Reddy, P.; Sarala Devi, G. [Inorganic and Physical Chemistry Division, Indian Institute Chemical Technology, Hyderabad 500607 (India); Sathiyaraj, S. [Department of Chemistry, Dr. NGP Institute of Technology, Coimbatore 641048, Tamil Nadu (India)

2016-01-15

Spinel ferrite (MnZnFe{sub 2}O{sub 4}, MnCuFe{sub 2}O{sub 4}, MnNiFe{sub 2}O{sub 4} and MnCoFe{sub 2}O{sub 4}) nanoparticles have been prepared by evaporation method. The annealing temperature plays an important role on changing particle size of the spinel ferrite nanoparticles was found out by X-ray diffraction and transmission electron microscopy. The role of manganese substitution in the spinel ferrite nanoparticles were also analyzed for different annealing temperature. The substitution of Mn also creates a vital change in dielectric properties have been measured in the frequency range of 100 kHz to 5 MHz. These spinel ferrites are decomposed to α-Fe{sub 2}O{sub 3} after annealing above 550 °C in air. Through the characterization of the prepared powder, the effect of annealing temperature, chemical composition and preparation technique on the microstructure, particle size and dielectric properties of the Mn substituted spinel ferrite nanoparticles are discussed. Furthermore, Conductance response of Mn substituted MFe{sub 2}O{sub 4} ferrite nanoparticles were measured by exposing the materials to reducing gas like liquefied petroleum gas (LPG). - Highlights: • The egg white support to achieve sample with shorter reaction time. • Manganese plays a significant role in sensor response. • Nature of the ferrites was affected with increasing annealing temperature.

Regolith-geology mapping with support vector machine: A case study over weathered Ni-bearing peridotites, New Caledonia

Science.gov (United States)

De Boissieu, Florian; Sevin, Brice; Cudahy, Thomas; Mangeas, Morgan; Chevrel, Stéphane; Ong, Cindy; Rodger, Andrew; Maurizot, Pierre; Laukamp, Carsten; Lau, Ian; Touraivane, Touraivane; Cluzel, Dominique; Despinoy, Marc

2018-02-01

Accurate maps of Earth's geology, especially its regolith, are required for managing the sustainable exploration and development of mineral resources. This paper shows how airborne imaging hyperspectral data collected over weathered peridotite rocks in vegetated, mountainous terrane in New Caledonia were processed using a combination of methods to generate a regolith-geology map that could be used for more efficiently targeting Ni exploration. The image processing combined two usual methods, which are spectral feature extraction and support vector machine (SVM). This rationale being the spectral features extraction can rapidly reduce data complexity by both targeting only the diagnostic mineral absorptions and masking those pixels complicated by vegetation, cloud and deep shade. SVM is a supervised classification method able to generate an optimal non-linear classifier with these features that generalises well even with limited training data. Key minerals targeted are serpentine, which is considered as an indicator for hydrolysed peridotitic rock, and iron oxy-hydroxides (hematite and goethite), which are considered as diagnostic of laterite development. The final classified regolith map was assessed against interpreted regolith field sites, which yielded approximately 70% similarity for all unit types, as well as against a regolith-geology map interpreted using traditional datasets (not hyperspectral imagery). Importantly, the hyperspectral derived mineral map provided much greater detail enabling a more precise understanding of the regolith-geological architecture where there are exposed soils and rocks.

A micro-scale investigation of melt production and extraction in the upper mantle based on silicate melt pockets in ultramafic xenoliths from the Bakony-Balaton Highland Volcanic Field (Western Hungary)

DEFF Research Database (Denmark)

Bali, Eniko; Zanetti, A.; Szabo, C.

2008-01-01

Mantle xenoliths in Neogene alkali basalts of the Bakony-Balaton Highland Volcanic Field (Western Hungary) frequently have melt pockets that contain silicate minerals, glass, and often carbonate globules. Textural, geochemical and thermobarometric data indicate that the melt pockets formed at rel...

Metasomatised ancient lithospheric mantle beneath the young Zealandia microcontinent and its role in HIMU-like intraplate magmatism

DEFF Research Database (Denmark)

Scott, James M; Waight, Tod Earle; van der Meer, Quinten

2014-01-01

There has been long debate on the asthenospheric versus lithospheric source for numerous intraplate basalts with ocean island basalt (OIB) and high time-integrated U/Pb (HIMU)-like source signatures that have erupted through the Zealandia continental crust. Analysis of 157 spinel facies peridotitic...... is highly heterogeneous. It is composed of a refractory craton-like domain (West Otago) adjacent to several moderately fertile domains (East Otago, North Otago, Auckland Islands). Each domain has an early history decoupled from the overlying Carboniferous and younger continental crust, and each domain has...

Rapid synthesis of monodispersed highly porous spinel nickel cobaltite (NiCo{sub 2}O{sub 4}) electrode material for supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Naveen, A. Nirmalesh, E-mail: nirmalesh.naveen@gmail.com; Selladurai, S. [Ionics Laboratory, Department of Physics, Anna University, Chennai-600025 (India)

2015-06-24

Monodispersed highly porous spinel nickel cobaltite electrode material was successfully synthesized in a short time using combustion technique. Single phase cubic nature of the spinel nickel cobaltite with average crystallite size of 24 nm was determined from X-ray diffraction study. Functional groups present in the compound were determined from FTIR study and it further confirms the spinel formation. FESEM images reveal the porous nature of the prepared material and uniform size distribution of the particles. Electrochemical evaluation was performed using Cyclic Voltammetry (CV) technique, Chronopotentiometry (CP) and Electrochemical Impedance Spectroscopy (EIS). Results reveal the typical pseudocapacitive behaviour of the material. Maximum capacitance of 754 F/g was calculated at the scan rate of 5 mV/s, high capacitance was due to the unique porous morphology of the electrode. Nyquist plot depicts the low resistance and good electrical conductivity of nickel cobaltite. It has been found that nickel cobaltite prepared by this typical method will be a potential electrode material for supercapcitor application.

The effects of stress concentrations on reaction progress: an example from experimental growth of magnesio-aluminate spinel at corundum - periclase interfaces under uniaxial load

Science.gov (United States)

Jerabek, Petr; Abart, Rainer; Rybacki, Erik; Habler, Gerlinde

2014-05-01

The study aims to understand the reaction progress and chemical, microstructural and textural evolution of magnesio-aluminate spinel reaction rims formed at varying experimental settings (load, temperature and experiment duration). The spinel rims were grown at the contacts between periclase and corundum at temperatures of 1250°C to 1350°C and dry atmosphere, maintained by a constant argon gas flow, under uniaxial load of 0.026 and 0.26 kN per 9 mm2 of initial contact area. Single crystals of periclase with [100] and of corundum with [0001] perpendicular to the polished reaction interface as well as polycrystalline corundum were used as starting materials. Two loading procedures, immediate application of the load before heating and loading after the desired temperature had been reached, were used. An important byproduct of our experiments stemmed from the immediate application of the load, which led to deformation twinning and fracturing of corundum. This internal deformation of corundum disturbed the reaction interface and introduced loci of concentrated stress due to opening of void spaces in between the reactant crystals. Whenever cracks formed in the initial stages of an experiment, the void space opened immediately and no spinel formed along these interface segments. In the case of deformation twinning, the decreased rim thickness indicates later opening of void spaces. This is because next to twins, the reaction interface is characterized by tight physical contact on the one side and less tight contact on the other side of the twin individual. The tight contacts are characterized by enhanced reaction progress which together with the overall positive volume change of the reaction and limits on plasticity of the studied phases led to the opening of void spaces at places characterized by less tight contacts. The thickness variations are less pronounced in our high load (0.26 kN) experiments where periclase behaves plastically and to some extent reduces the

Solution-combustion synthesized aluminium-doped spinel (LiAl(subx)Mn(sub2-x)O(sub4) as a high-performance lithium-ion battery cathode material

CSIR Research Space (South Africa)

Kebede, MA

2015-06-01

Full Text Available High-performing (LiAl(subx)Mn(sub2-x)O(sub4) (x = 0, 0.125, 0.25, 0.375, and 0.5) spinel cathode materials for lithium-ion battery were developed using a solution combustion method. The as-synthesized cathode materials have spinel cubic structure...

Microwave-assisted synthesis of high-voltage nanostructured LiMn1.5Ni0.5O4 spinel: tuning the Mn3+ content and electrochemical performance

CSIR Research Space (South Africa)

Jafta, CJ

2013-08-01

Full Text Available on the Mn3+ concentration and electrochemistry of the LiMn1.5Ni0.5O4 spinel. It is shown that microwave is capable of tuning the Mn3+ content of the spinel for enhanced electrochemical performance (high capacity, high capacity retention, excellent rate...

Studying magnetic structure of Bi doped Co2MnO4 cubic spinel by neutron diffraction

International Nuclear Information System (INIS)

Rajeevan, N.E.; Kaushik, S.D.; Kumar, Ravi

2016-01-01

In present work, we studied effect of Bi doped spinel Bi x Co 2-x MnO 4 (x = 0, 0.05, 0.10, 0.15 and 0.20) samples on their crystal as well as magnetic structure by employing neutron diffraction of wavelength 1.48 A using focusing crystal diffractometer of UGC-DAECSR Mumbai Centre at Dhruva, Trombay, Mumbai, India. The analysis of the neutron diffraction using Fullprof program reveals that crystal structure due to Bi doping remains intact and all the samples have been formed in the cubic spinel structure with Fd3m (space group no. 227). The lattice parameter shows the positive thermal expansion upon Bi doping across the temperature range. In order to understand the implication on the spin structure and magnetism in the detail, temperature dependent neutron diffraction study is carried out on some of the samples (x = 0, 0.1) in the series. The ND pattern of x = 0.1 at 2.9K is shown. The experimental finding in terms of modified magnetic structure upon Bi doping are discussed which are understood in terms of variation in the ferroelectric properties, bond lengths and their effect on the CoO 6 polyhedra. Furthermore, Bi substitution in Co 2 MnO 4 spinel brings in the balance of structural distortion, which affects both ferrimagnetism and ferroelectricity

Recycling Spent Primary Cells for the Synthesis of Spinel ZnMn 2 O ...

African Journals Online (AJOL)

The mixture was then placed in a fireclay crucible and irradiated in a domestic microwave oven (Pioneer, Model PM-25 L, 2450 MHz, 1000 W) for 20 minutes and reaction products were separated and characterised. Spherical particles of spinel zinc manganese oxide (ZnMn2O4) were isolated after crushing the reduced ...

Origin of peraluminous minerals (corundum, spinel, and sapphirine) in a highly calcic anorthosite from the Sittampundi Layered Complex, Tamil Nadu, India

Science.gov (United States)

Karmakar, Shreya; Mukherjee, Subham; Sanyal, Sanjoy; Sengupta, Pulak

2017-08-01

The highly calcic anorthosite (An>95) from the Sittampundi Layered Complex (SLC) develops corundum, spinel and sapphirine that are hitherto not reported from any anorthositic rocks in the world. Petrological observations indicate the following sequence of mineral growth: plagioclasematrix → corundum; clinopyroxene → amphibole; corundum + amphibole → plagioclasecorona + spinel; and spinel + corundum → coronitic sapphirine. Phase relations in the CaO-Na2O-Al2O3-SiO2-H2O (CNASH) system suggest that corundum was presumably developed through vapour present incongruent melting of the highly calcic plagioclase during ultra-high temperature (UHT) metamorphism ( T ≥ 1000 °C, P ≥ 9 kbar). Topological constraints in parts of the Na2O-CaO-MgO-Al2O3-SiO2-H2O (NCMASH) system suggest that subsequent to the UHT metamorphism, aqueous fluid(s) permeated the rock and the assemblage corundum + amphibole + anorthite + clinozoisite was stabilized during high-pressure (HP) metamorphism (11 ± 2 kbar, 750 ± 50 °C). Constraints of the NCMASH topology and thermodynamic and textural modeling study suggest that coronitic plagioclase and spinel formed at the expense of corundum + amphibole during a steeply decompressive retrograde P- T path (7-8 kbar and 700-800 °C) in an open system. Textural modeling studies combined with chemical potential diagrams (μSiO2-μMgO) in the MASH system support the view that sapphirine also formed from due to silica and Mg metasomatism of the precursor spinel ± corundum, on the steeply decompressive retrograde P- T path, prior to onset of significant cooling of the SLC. Extremely channelized fluid flow and large positive solid volume change of the stoichiometrically balanced sapphirine forming reaction explains the localized growth of sapphirine.

Spinels of Variscan olivine hornblendites related to the Montnegre granitoids revisited (NE Spain): petrogenetic evidence of mafic magma mixing

Energy Technology Data Exchange (ETDEWEB)

Galán, G.; Enrique, P.; Butjosa, L.; Fernández-Roig, L.

2017-07-01

Olivine hornblendites (cortlandtites) form part of the Montnegre mafic complex related to late-Variscan I-type granitoids in the Catalan Coastal Ranges. Two generations of spinel are present in these hornblendites: Spl1 forms euhedral crystals included in both olivine and Spl2. Spl2 forms euhedral to anhedral crystals associated with phlogopite and fibrous colourless amphibole forming pseudomorphs after olivine. Compositions of Spl1 are picotite-Al chromite (Fe#: 77.78-66.60; Cr#: 30.12-52.22; Fe3+/R3+: 6.99-21.89; 0.10< TiO2%< 0.62). Compositions of Spl2 are pleonaste (Fe#: 37.86-52.12; Cr#: 1.00-15.45; Fe3+/R3+: 0.31-5.21; TiO2% <0.10%). The two types of spinel follow a CrAl trend, mainly due to the substitution (Fe2+)-1Cr-1= MgAl, which is interpreted as the result of mixing between two different mantle-derived melts. The compositions of early Spl1 crystals included in olivine are characteristic of Al-rich basalts. More aluminous Spl2 would result from reaction of olivine with a less evolved, Al and K-rich mantle-derived melt after new refilling of the magma chamber or channel. As a whole, spinels from similar examples of Variscan olivine hronblendites also follow a CrAl trend with high Fe# and starting at higher Cr# than other trends of this type. Cr# heterogeneity in the early spinels from these Variscan hornblendites would be inherited from the variable Al content of the mafic melts involved in their genesis.

Effect of the preparation method on the structural and catalytic properties of spinel cobalt-iron oxide

Energy Technology Data Exchange (ETDEWEB)

Hammiche-Bellal, Yasmina, E-mail: yasminahammiche@gmail.com [Laboratoire des Matériaux Catalytiques et Catalyse en Chimie Organique, Faculté de Chimie, USTHB, BP32 El Alia, Bab Ezzouar, 16111, Alger (Algeria); Djadoun, Amar [Laboratoire de Géophysique, FSTGAT, USTHB, BP32 El Alia, Bab Ezzouar, 16111, Alger (Algeria); Meddour-Boukhobza, Laaldja; Benadda, Amel [Laboratoire des Matériaux Catalytiques et Catalyse en Chimie Organique, Faculté de Chimie, USTHB, BP32 El Alia, Bab Ezzouar, 16111, Alger (Algeria); Auroux, Aline [Université Lyon 1, CNRS, UMR 5256, IRCELYON, Institut de Recherches sur la Catalyse et l' Environnement de Lyon, 2 Avenue Albert Einstein, F-69626, Villeurbanne (France); Berger, Marie-Hélène [Centre des Matériaux PIERRE-MARIE Fourt, UMR 7633, Paris (France); Mernache, Fateh [UDEC-CRND, COMENA, BP 43 Draria, 16050, Alger (Algeria)

2016-07-01

Spinel cobalt-iron oxide was synthesized by co-precipitation and hydrothermal routes. The effect of the co-precipitation experimental conditions, the calcination temperature and the hydrothermal synthesis time and temperature on the properties of the solids was studied. The prepared powders were evaluated as catalysts in the ethanol combustion reaction, and were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM/EDX), nitrogen adsorption–desorption isotherms (BET, BJH) and temperature programmed reduction (TPR) techniques. Using chloride salts as starting materials and sodium hydroxide as precipitating agent, the CoFe{sub 2}O{sub 4} prepared powders displayed a mesoporous structure with a pore distribution strongly dependent on the experimental conditions. A monophasic spinel phase in the case of the calcined solids was obtained while the hydrothermal process led to the formation of a mixture of single oxides in addition to the spinel phase. The variation of the crystallite size and the lattice parameter as a function of calcination temperature was similar, whereas this variation found to be irregular when the synthesis residence time in autoclave was increased. The hydrothermally treated solids show the best catalytic performance in the total oxidation of ethanol. The catalytic behavior was correlated with the crystallite size and the reduction temperature of cobalt species determined by the TPR analysis. - Highlights: • Pure CoFe{sub 2}O{sub 4} phase is obtained by co-precipitation method at calcination temperatures 500–900 °C. • The temperature of co-precipitation procedure influences strongly the growth of the solids during the calcination step. • The hydrothermal synthesis gives a mixture of oxides; CoFe{sub 2}O{sub 4} is the predominant phase. • The CoFe{sub 2}O{sub 4} spinel showed a good catalytic reactivity in the ethanol combustion reaction. • The catalysts prepared by hydrothermal process are more reactive and

Potential Temperatures of Sources of MORB, OIB and LIPs Based on AL Partitioning Between Olivine and Spinel

Science.gov (United States)

Sobolev, A. V.; Batanova, V. G.; Krasheninnikov, S.; Borisov, A.; Arndt, N.; Kuzmin, D.; Krivolutskaya, N.; Sushevskaya, N.

2013-12-01

Knowledge of potential temperatures of convecting mantle is required for the understanding the global processes on the Earth [1]. The common way to estimate these is the reconstruction of primary melt compositions and liquidus temperatures based on the Fe-Mg partitioning between olivine and melt. This approach requires knowledge of the compositions of primitive melts in equilibrium with olivine alone as well as composition of olivine equilibrium with primary melts. This information is in most cases unavailable or of questionable quality. Here we report a new approach to obtain crystallization temperatures of primary melts based on the olivine-spinel Al-Cr geothermometer [2]. The advantages of this approach are: (1) low rate of diffusion of Al in the olivine, which promises to preserve high magmatic temperatures and (2) common presence of spinel in assemblage with high-Mg olivine. In order to decipher influence of elevated Ti concentrations in spinel we have run several experiments at high temperatures (1400-1200 degree C), atmospheric pressure and controled oxygen fugacity. We also analysed over two thousand spinel inclusions and high-Mg host olivines from different MORB, OIB, LIP and Archean komatiites on the JXA-8230 EPMA at ISTerre, Grenoble, France. Concentrations of Al, Ti, Na, P, Zn, Cr, Mn, Ca, Co, Ni were determined with a precision of 10 ppm (2 standard errors) using a newly developed protocol [3]. When available, we also analysed matrix glass and glass inclusions in olivine and found that temperature estimations from olivine-spinel (Al-Cr) and olivine-melt (Fe-Mg) [4] equilibrium match within (+/-30 degree C). The results show contrasting crystallization temperatures of Mg-rich olivine of the same Fo content from different types of mantle-derived magmas, from the lowest (down to 1220 degree C) for MORB to the highest (up to 1550 degree C) for komatiites and Siberian meimechites. These results match predictions from Fe-Mg olivine-melt equilibrium and

Re4As6S3, a thio-spinel-related cluster system

DEFF Research Database (Denmark)

Besnard, Celine; Svensson, Christer; Ståhl, Kenny

2003-01-01

. The rhenium atoms form tetrahedral clusters linked via tetrahedral arsenic clusters to produce an NaCl-type arrangement. The oxidation state of rhenium is IV and the number of electrons shared by the rhenium atoms in the cluster is 12. The structure is based on an ordered defect thio-spinel A((1-x))B(2)X(4......) where the B-type atoms form tetrahedral clusters....

Solid-liquid phase equilibria of Fe-Cr-Al alloys and spinels

Science.gov (United States)

McMurray, J. W.; Hu, R.; Ushakov, S. V.; Shin, D.; Pint, B. A.; Terrani, K. A.; Navrotsky, A.

2017-08-01

Ferritic FeCrAl alloys are candidate accident tolerant cladding materials. There is a paucity of data concerning the melting behavior for FeCrAl and its oxides. Analysis tools have therefore had to utilize assumptions for simulations using FeCrAl cladding. The focus of this study is to examine in some detail the solid-liquid phase equilibria of FeCrAl alloys and spinels with the aim of improving the accuracy of severe accident scenario computational studies.

Paleozoic and Paleoproterozoic Zircon in Igneous Xenoliths Assimilated at Redoubt Volcano, Alaska

Science.gov (United States)

Bacon, C. R.; Vazquez, J. A.; Wooden, J. L.

2010-12-01

Historically active Redoubt Volcano is a basalt-to-dacite cone constructed upon the Jurassic-early Tertiary Alaska-Aleutian Range batholith. New SHRIMP-RG U-Pb age and trace-element concentration results for zircons from gabbroic xenoliths and crystal-rich andesitic mush from a late Pleistocene pyroclastic deposit indicate that ~310 Ma and ~1865 Ma igneous rocks underlie Redoubt at depth. Two gabbros have sharply terminated prismatic zircons that yield ages of ~310 Ma. Zircons from a crystal mush sample are overwhelmingly ~1865 Ma and appear rounded due to incomplete dissolution. Binary plots of element concentrations or ratios show clustering of data for ~310-Ma grains and markedly coherent trends for ~1865-Ma grains; e.g., ~310-Ma grains have higher Eu/Eu* than most of the ~1865-Ma grains, the majority of which form a narrow band of decreasing Eu/Eu* with increasing Hf content which suggests that ~1865-Ma zircons come from igneous source rocks. It is very unlikely that detrital zircons from a metasedimentary rock would have this level of homogeneity in age and composition. One gabbro contains abundant ~1865 Ma igneous zircons, ~300-310 Ma fluid-precipitated zircons characterized by very low U and Th concentrations and Th/U ratios, and uncommon ~100 Ma zircons. We propose that (1) ~310 Ma gabbro xenoliths from Redoubt Volcano belong to the same family of plutons dated by Aleinikoff et al. (USGS Circular 1016, 1988) and Gardner et al. (Geology, 1988) located ≥500 km to the northeast in basement rocks of the Wrangellia and Alexander terranes and (2) ~1865 Ma zircons are inherited from igneous rock, potentially from a continental fragment that possibly correlates with the Fort Simpson terrane or Great Bear magmatic zone of the Wopmay Orogen of northwestern Laurentia. Possibly, elements of these Paleoproterozoic terranes intersected the Paleozoic North American continental margin where they may have formed a component of the basement to the Wrangellia

Melts of garnet lherzolite: experiments, models and comparison to melts of pyroxenite and carbonated lherzolite

Science.gov (United States)

Grove, Timothy L.; Holbig, Eva S.; Barr, Jay A.; Till, Christy B.; Krawczynski, Michael J.

2013-01-01

Phase equilibrium experiments on a compositionally modified olivine leucitite from the Tibetan plateau have been carried out from 2.2 to 2.8 GPa and 1,380–1,480 °C. The experiments-produced liquids multiply saturated with spinel and garnet lherzolite phase assemblages (olivine, orthopyroxene, clinopyroxene and spinel ± garnet) under nominally anhydrous conditions. These SiO2-undersaturated liquids and published experimental data are utilized to develop a predictive model for garnet lherzolite melting of compositionally variable mantle under anhydrous conditions over the pressure range of 1.9–6 GPa. The model estimates the major element compositions of garnet-saturated melts for a range of mantle lherzolite compositions and predicts the conditions of the spinel to garnet lherzolite phase transition for natural peridotite compositions at above-solidus temperatures and pressures. We compare our predicted garnet lherzolite melts to those of pyroxenite and carbonated lherzolite and develop criteria for distinguishing among melts of these different source types. We also use the model in conjunction with a published predictive model for plagioclase and spinel lherzolite to characterize the differences in major element composition for melts in the plagioclase, spinel and garnet facies and develop tests to distinguish between melts of these three lherzolite facies based on major elements. The model is applied to understand the source materials and conditions of melting for high-K lavas erupted in the Tibetan plateau, basanite–nephelinite lavas erupted early in the evolution of Kilauea volcano, Hawaii, as well as younger tholeiitic to alkali lavas from Kilauea.

A subduction wedge origin for Paleoarchean peridotitic diamonds and harzburgites from the Panda kimberlite, Slave craton: evidence from Re-Os isotope systematics

Science.gov (United States)

Westerlund, K. J.; Shirey, S. B.; Richardson, S. H.; Carlson, R. W.; Gurney, J. J.; Harris, J. W.

2006-09-01

An extensive study of peridotitic sulfide inclusion bearing diamonds and their prospective harzburgitic host rocks from the 53 Ma Panda kimberlite pipe, Ekati Mine, NWT Canada, has been undertaken with the Re-Os system to establish their age and petrogenesis. Diamonds with peridotitic sulfide inclusions have poorly aggregated nitrogen (bearing diamonds and indicates residence in the cooler portion of the Slave craton lithospheric mantle. For most of the sulfide inclusions, relatively low Re contents (average 0.457 ppm) and high Os contents (average 339 ppm) lead to extremely low 187Re/188Os, typically << 0.05. An age of 3.52 ± 0.17 Ga (MSWD = 0.46) and a precise initial 187Os/188Os of 0.1093 ± 0.0001 are given by a single regression of 11 inclusions from five diamonds that individually provide coincident internal isochrons. This initial Os isotopic composition is 6% enriched in 187Os over 3.5 Ga chondritic or primitive mantle. Sulfide inclusions with less radiogenic initial Os isotopic compositions reflect isotopic heterogeneity in diamond forming fluids. The harzburgites have even lower initial 187Os/188Os than the sulfide inclusions, some approaching the isotopic composition of 3.5 Ga chondritic mantle. In several cases isotopically distinct sulfides occur in different growth zones of the same diamond. This supports a model where C-O-H-S fluids carrying a radiogenic Os signature were introduced into depleted harzburgite and produced diamonds containing sulfides conforming to the 3.5 Ga isochron. Reaction of this fluid with harzburgite led to diamonds with less radiogenic inclusions while elevating the Os isotope ratios of some harzburgites. Subduction is a viable way of introducing such fluids. This implies a role for subduction in creating early continental nuclei at 3.5 Ga and generating peridotitic diamonds.

Crustal evolution at mantle depths constrained from Pamir xenoliths

Science.gov (United States)

Kooijman, E.; Hacker, B. R.; Smit, M. A.; Kylander-Clark, A. R.; Ratschbacher, L.

2012-12-01

Lower crustal xenoliths erupted in the Pamir at ~11 Ma provide an exclusive opportunity to study the evolution of crust at mantle depths during a continent-continent collision. To investigate, and constrain the timing of, the petrologic processes that occurred during burial to the peak conditions (2.5-2.8 GPa, 1000-1100 °C; [1]), we performed chemical- and isotope analyses of accessory minerals in 10 xenoliths, ranging from eclogites to grt-ky-qtz granulites. In situ laser ablation split-stream ICPMS yielded 1) U-Pb ages, Ti concentrations and REE in zircon, 2) U/Th-Pb ages and REE in monazite, and 3) U-Pb ages and trace elements in rutile. In addition, garnet, and biotite and K-feldspar were dated using Lu-Hf and 40Ar/39Ar geochronology, respectively. Zircon and monazite U-(Th-)Pb ages are 101.9±1.8, 53.7±1.0, 39.1±0.8, 21.7±0.4, 18.2±0.5, 16.9±0.8, 15.1±0.3 (2σ) and 12.5-11.1 Ma; most samples showed several or all of these populations. The 53.7 Ma and older ages are xenocrystic or detrital. For younger ages, zircon and monazite in individual samples recorded different ages-although zircon in one rock and monazite in another can be the same age. The 39.1 Ma zircon and monazite mostly occur as inclusions in minerals of the garnet-bearing assemblage that represents the early, low-P stages of burial. Garnet Lu-Hf ages of 37.8±0.3 Ma support garnet growth at this time. Spinifex-like textures containing 21.7-11.1 Ma zircon and monazite record short-lived partial melting events during burial. Aligned kyanite near these patches indicates associated deformation. Zircons yielding ≤12.5 Ma exhibit increased Eu/Eu* and markedly decreased HREE concentrations, interpreted to record feldspar breakdown and omphacite growth during increasing pressure. Rutile U-Pb cooling ages are 10.8±0.3 Ma in all samples. This agrees with the weighted mean 40Ar/39Ar age of eight biotite, K-feldspar and whole rock separates of 11.00+0.16/-0.09 Ma. Rutile in eclogites provides Zr

Crystal field and site deformation in spinels and pentavalent uranium compounds

International Nuclear Information System (INIS)

Drifford, M.; Soulie, E.

1976-01-01

Magnesium aluminates with different alumina contents have the spinel structure. The optical absorption spectra of doped spinel compounds (Cr 3+ , Ni 2+ , Co 2+ ) or E.S.R. spectra (Cr 3+ , Mn 2+ ) are used for the investigation of the position of the doping materials and the deformation of the crystal sites, and give information on the structural disorders. The local structural information given by the doping materials are compared with the mean structure parameters obtained from X-ray diffraction. The optical absorption spectrum and the principal components of the g tensor for UF 6 Cs and the thermal variation in the magnetic susceptibility for UF 8 Cs 3 and UF 8 (NH 4 ) are used for determining the parameters of the electron Hamiltonian for the f 1 configuration. A rather significant covalent aspect is evidenced for UF 6 Cs, in the framework of the model of Eisenstein and Pryce, this property being weaker for the other two complex compounds. The three parameters giving the crystal field at a deformed cubic site with Dsub(3d) symmetry in the Newman superposition model are noticeably weaker for the 8-coordination than for the 6-coordination. As for UF 8 Cs 3 and UF 8 (NH 4 ) 3 a calculation predicts an electronic levels with a very low excitation, at about 110 and 70cm -1 respectively [fr

P-type zinc oxide spinels: application to transparent conductors and spintronics

International Nuclear Information System (INIS)

Stoica, Maria; S Lo, Cynthia

2014-01-01

We report on the electronic and optical properties of two theoretically predicted stable spinel compounds of the form ZnB 2 O 4 , where B = Ni or Cu; neither compound has been previously synthesized, so we compare them to the previously studied p-type ZnCo 2 O 4 spinel. These new materials exhibit spin polarization, which is useful for spintronics applications, and broad conductivity maxima near the valence band edge that indicate good p-type dopability. We show that 3d electrons on the octahedrally coordinated Zn atom fall deep within the valence band and do not contribute significantly to the electronic structure near the band edge of the material, while the O 2p and tetrahedrally coordinated B 3d electrons hybridize broadly in the shallow valence states, resulting in increasing curvature (i.e., decreased electron effective mass) of valence bands near the band edge. In particular, ZnCu 2 O 4 exhibits high electrical conductivities in the p-doping region near the valence band edge that, at σ=2×10 4  S cm −1 , are twice the maximum found for ZnCo 2 O 4 , a previously synthesized compound in this class of materials. This material also exhibits ferromagnetism in all of its most stable structures, which makes it a good candidate for further study as a dilute magnetic semiconductor. (paper)

Plasma sprayed manganeseecobalt spinel coatings: Process sensitivity on phase, electrical and protective performance

Czech Academy of Sciences Publication Activity Database

Han Jung, S.; Pala, Zdeněk; Sampath, S.

2016-01-01

Roč. 304, February (2016), s. 234-243 ISSN 0378-7753 R&D Projects: GA ČR GB14-36566G Institutional support: RVO:61389021 Keywords : Interconnect protection * Cr-poisoning * Manganese cobalt spinel * Electrical conductivity * Plasma spray Subject RIV: JE - Non-nuclear Energetics, Energy Consumption ; Use Impact factor: 6.395, year: 2016 http://www.sciencedirect.com/science/article/pii/S0378775315305383

Ab initio investigation of the thermodynamics of cation distribution and of the electronic and magnetic structures in the LiMn2O4 spinel

Science.gov (United States)

Santos-Carballal, David; Ngoepe, Phuti E.; de Leeuw, Nora H.

2018-02-01

The spinel-structured lithium manganese oxide (LiMn2O4 ) is a material currently used as cathode for secondary lithium-ion batteries, but whose properties are not yet fully understood. Here, we report a computational investigation of the inversion thermodynamics and electronic behavior of LiMn2O4 derived from spin-polarized density functional theory calculations with a Hubbard Hamiltonian and long-range dispersion corrections (DFT+U-D3). Based on the analysis of the configurational free energy, we have elucidated a partially inverse equilibrium cation distribution for the LiMn2O4 spinel. This equilibrium degree of inversion is rationalized in terms of the crystal field stabilization effects and the difference between the size of the cations. We compare the atomic charges with the oxidation numbers for each degree of inversion. We found segregation of the Mn charge once these ions occupy the tetrahedral and octahedral sites of the spinel. We have obtained the atomic projections of the electronic band structure and density of states, showing that the normal LiMn2O4 has half-metallic properties, while the fully inverse spinel is an insulator. This material is in the ferrimagnetic state for the inverse and partially inverse cation arrangement. The optimized lattice and oxygen parameters, as well as the equilibrium degree of inversion, are in agreement with the available experimental data. The partial equilibrium degree of inversion is important in the interpretation of the lithium ion migration and surface properties of the LiMn2O4 spinel.

Rheological properties of the lower crust and upper mantle beneath Baja California: a microstructural study of xenoliths from San Quintin

Science.gov (United States)

Van der Werf, Thomas F.; Chatzaras, Vasileios; Tikoff, Basil; Drury, Martyn R.

2016-04-01

Baja California is an active transtensional rift zone, which links the San Andreas Fault with the East Pacific Rise. The erupted basalts of the Holocene San Quintin volcanic field contain xenoliths, which sample the lower crust and upper mantle beneath Baja California. The aim of this research is to gain insight in the rheology of the lower crust and the upper mantle by investigating the xenolith microstructure. Microstructural observations have been used to determine the dominant deformation mechanisms. Differential stresses were estimated from recrystallized grain size piezometry of plagioclase and clinopyroxene for the lower crust and olivine for the upper mantle. The degree of deformation can be inferred from macroscopic foliations and the deformation microstructures. Preliminary results show that both the lower crust and the upper mantle have been affected by multiple stages of deformation and recrystallization. In addition the dominant deformation mechanism in both the lower crust and the upper mantle is dislocation creep based on the existence of strong crystallographic preferred orientations. The differential stress estimates for the lower crust are 10-29 MPa using plagioclase piezometry and 12-35 MPa using clinopyroxene piezometry. For the upper mantle, differential stress estimates are 10-20 MPa. These results indicate that the strength of the lower crust and the upper mantle are very similar. Our data do not fit with the general models of lithospheric strength and may have important implications for the rheological structure of the lithosphere in transtensional plate margins and for geodynamic models of the region.

Towards a lattice-matching solid-state battery: synthesis of a new class of lithium-ion conductors with the spinel structure.

Science.gov (United States)

Rosciano, Fabio; Pescarmona, Paolo P; Houthoofd, Kristof; Persoons, Andre; Bottke, Patrick; Wilkening, Martin

2013-04-28

Lithium ion batteries have conquered most of the portable electronics market and are now on the verge of deployment in large scale applications. To be competitive in the automotive and stationary sectors, however, they must be improved in the fields of safety and energy density (W h L(-1)). Solid-state batteries with a ceramic electrolyte offer the necessary advantages to significantly improve the current state-of-the-art technology. The major limit towards realizing a practical solid-state lithium-ion battery lies in the lack of viable ceramic ionic conductors. Only a few candidate materials are available, each carrying a difficult balance between advantages and drawbacks. Here we introduce a new class of possible solid-state lithium-ion conductors with the spinel structure. Such compounds could be coupled with spinel-type electrode materials to obtain a "lattice matching" solid device where low interfacial resistance could be achieved. Powders were prepared by wet chemistry, their structure was studied by means of diffraction techniques and magic angle spinning NMR, and Li(+) self-diffusion was estimated by static NMR line shape measurements. Profound differences in the Li(+) diffusion properties were observed depending on the composition, lithium content and cationic distribution. Local Li(+) hopping in the spinel materials is accompanied by a low activation energy of circa 0.35 eV being comparable with that of, e.g., LLZO-type garnets, which represent the current benchmark in this field. We propose these novel materials as a building block for a lattice-matching all-spinel solid-state battery with low interfacial resistance.

Stagnation and Storage of Strongly Depleted Melts in Slow-Ultraslow Spreading Oceans: Evidence from the Ligurian Tethys

Science.gov (United States)

Piccardo, Giovanni; Guarnieri, Luisa; Padovano, Matteo

2013-04-01

Our studies of Alpine-Apennine ophiolite massifs (i.e., Lanzo, Voltri, Ligurides, Corsica) show that the Jurassic Ligurian Tethys oceanic basin was a slow-ultraslow spreading basin, characterized by the exposures on the seafloor of mantle peridotites with extreme compositional variability. The large majority of these peridotites are made of depleted spinel harzburgites and plagioclase peridotites. The former are interpreted as reactive peridotites formed by the reactive percolation of under-saturated, strongly trace element depleted asthenospheric melts migrated by porous flow through the mantle lithosphere. The latter are considered as refertilized peridotites formed by peridotite impregnation by percolated silica-saturated, strongly trace element depleted melts. Strongly depleted melts were produced as low-degrees, single melt increments by near fractional melting of the passively upwelling asthenosphere during the rifting stage of the basin. They escaped single melt increment aggregation, migrated isolated through the mantle lithosphere by reactive porous or channeled flow before oceanic opening, and were transformed into silica-saturated derivative liquids that underwent entrapment and stagnation in the shallow mantle lithosphere forming plagioclase-enriched peridotites. Widespread small bodies of strongly depleted gabbro-norites testify for the local coalescence of these derivative liquids. These melts never reached the surface (i.e., the hidden magmatism), since lavas with their composition have never been found in the basin. Subsequently, aggregated MORB melts upwelled within replacive dunite channels (as evidenced by composition of magmatic clinopyroxenes in dunites), intruded at shallow levels as olivine gabbro bodies and extruded as basaltic lavas, to form the crustal rocks of the oceanic lithosphere (i.e., the oceanic magmatism). Km-scale bodies of MORB olivine gabbros were intruded into the plagioclase-enriched peridotites, which were formed in the

Observation of large low-field magnetoresistance in spinel cobaltite: A new half-metal

KAUST Repository

Li, Peng

2015-12-10

Low-field magnetoresistance is an effective and energy-saving way to use half-metallic materials in magnetic reading heads and magnetic random access memory. Common spin-polarized materials with low field magnetoresistance effect are perovskite-type manganese, cobalt, and molybdenum oxides. In this study, we report a new type of spinel cobaltite materials, self-assembled nanocrystalline NiCo2O4, which shows large low field magnetoresistance as large as –19.1% at 0.5 T and –50% at 9 T (2 K). The large low field magnetoresistance is attributed to the fast magnetization rotation of the core nanocrystals. The surface spin-glass is responsible for the observed weak saturation of magnetoresistance under high fields. Our calculation demonstrates that the half-metallicity of NiCo2O4 comes from the hopping eg electrons within the tetrahedral Co-atoms and the octahedral Ni-atoms. The discovery of large low-field magnetoresistance in simple spinel oxide NiCo2O4, a non-perovskite oxide, leads to an extended family of low-field magnetoresistance materials. (© 2016 WILEY-VCH Verlag GmbH &Co. KGaA, Weinheim)

Observation of large low-field magnetoresistance in spinel cobaltite: A new half-metal

KAUST Repository

Li, Peng; Xia, Chuan; Zheng, Dongxing; Wang, Ping; Jin, Chao; Bai, Haili

2015-01-01

Low-field magnetoresistance is an effective and energy-saving way to use half-metallic materials in magnetic reading heads and magnetic random access memory. Common spin-polarized materials with low field magnetoresistance effect are perovskite-type manganese, cobalt, and molybdenum oxides. In this study, we report a new type of spinel cobaltite materials, self-assembled nanocrystalline NiCo2O4, which shows large low field magnetoresistance as large as –19.1% at 0.5 T and –50% at 9 T (2 K). The large low field magnetoresistance is attributed to the fast magnetization rotation of the core nanocrystals. The surface spin-glass is responsible for the observed weak saturation of magnetoresistance under high fields. Our calculation demonstrates that the half-metallicity of NiCo2O4 comes from the hopping eg electrons within the tetrahedral Co-atoms and the octahedral Ni-atoms. The discovery of large low-field magnetoresistance in simple spinel oxide NiCo2O4, a non-perovskite oxide, leads to an extended family of low-field magnetoresistance materials. (© 2016 WILEY-VCH Verlag GmbH &Co. KGaA, Weinheim)

Melt inclusion: methods, applications and problem: Silica-rich melts in quartz xenoliths from Vulcano islands and their bearing on processes of crustal melting and crust-magma interaction in the Aeolian Arc, Italy

NARCIS (Netherlands)

Frezzotti, M.L.; Zavon, V.; Peccerillo, A.; Nikogosian, I.

2002-01-01

Silica-rich melts in quartz xenoliths from Vulcano islands and their bearing on processes of crustal melting and crust-magma interaction in the Aeolian Arc, Italy Proceedings of workshop Melt inclusion: methods, applications and problem. Napoli, Italy, September 2002, p. 71-73

Synthesis and magnetic properties of CoFe2O4 spinel ferrite nanoparticles doped with lanthanide ions

International Nuclear Information System (INIS)

Kahn, Myrtil L.; Zhang, Z. John

2001-01-01

Lanthanide ions have been doped into cobalt spinel ferrites using an oil-in-water micellar method to form CoLn 0.12 Fe 1.88 O 4 nanoparticles with Ln=Ce, Sm, Eu, Gd, Dy, or Er. Doping with lanthanide ions (Ln III ) modulates the magnetic properties of cobalt spinel ferrite nanoparticles. In particular cases of Gd 3+ or Dy 3+ ions, a dramatic increase in the blocking temperature and coercivity is observed. Indeed, the introduction of only 4% of Gd 3+ ions increases the blocking temperature ∼100 K and the coercivity 60%. Initial studies on the magnetic properties of these doped nanoparticles clearly demonstrate that the relationship between the modulation of magnetic properties and the nature of doped Ln III ions is interesting but very complex. [copyright] 2001 American Institute of Physics

Accessory priderite and burbankite in multiphase solid inclusions in the orogenic garnet peridotite from the Bohemian Massif, Czech Republic

Czech Academy of Sciences Publication Activity Database

Naemura, K.; Shimizu, I.; Svojtka, Martin; Hirajima, T.

2015-01-01

Roč. 110, č. 1 (2015), s. 20-28 ISSN 1345-6296 Grant - others:Rada Programu interní podpory projektů mezinárodní spolupráce AV ČR(CZ) M100131203 Program:Program interní podpory projektů mezinárodní spolupráce AV ČR Institutional support: RVO:67985831 Keywords : garnet peridotite * Variscan orogeny * multiphase solid inclusion * priderite * burbankite Subject RIV: DB - Geology ; Mineralogy Impact factor: 0.648, year: 2015

6Li MAS NMR Study of Lithium Insertion into Hydrothermally Prepared Li-Ti-O Spinel

Czech Academy of Sciences Publication Activity Database

Krtil, Petr; Dědeček, Jiří; Kostlánová, Tereza; Brus, Jiří

2004-01-01

Roč. 7, č. 7 (2004), A163-A166 ISSN 1099-0062 R&D Projects: GA ČR GA203/03/0823 Institutional research plan: CEZ:AV0Z4040901 Keywords : lithium insertion * spinel * NMR Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.271, year: 2004

Effects of γ-irradiation upon the optical behavior of spinel

International Nuclear Information System (INIS)

White, G.S.; Lee, K.H.; Crawford, J.H.Jr.

1977-01-01

The effect of 137 Cs gamma irradiation (0.67 MeV photons) upon the optical absorption and thermoluminescence of spinel (MgAl 2 O 4 ) is studied. Exposure to gamma radiation provides electrons which are captured at Fesup(3+) in octahedral sites, thereby producing Fesup(2+) and destroying the 4.8 and 6.4 eV absorption bands. Isochronal annealing curves of the 3.1 and 4.8 eV peaks are given. A reciprocal relationship between the recovery of the 4.8 eV band and the thermoluminescence immediately after irradiation and after sitting over night has been measured

Synthesis of {gamma}-aluminium oxynitride spinel using thermal plasma technique

Energy Technology Data Exchange (ETDEWEB)

Panda, Pravuram; Singh, S. K.; Sinha, S. P. [School of Applied Science (Physics), KIIT University, Bhubaneswar 751024 (India); Advanced Materials Technology Department, IMMT (CSIR), Bhubaneswar 751013 (India); School of Applied Science (Physics), KIIT University, Bhubaneswar 751024 (India)

2012-07-23

The synthesis technique of {gamma}-AlON in NH{sub 3} plasma using extended arc thermal plasma reactor have been reported. Dense cubic AlON spinel was synthesized in liquid state by fusion of mixture of Al{sub 2}O{sub 3} and AlN powder under thermal plasma. The density of the fused AlON was found to be 3.64 g/cc which is 98.11% of theoretical value. The formation of AlON was confirmed from XRD and Raman studies. Well faceted structure of plasma fused AlON was observed in FE-SEM micrograph.

The behavior of mineral inclusions during host decomposition. A SEM-STEM study of rutile inclusions at a natural propagating corundum-spinel interface.

Science.gov (United States)

Baldwin, Lisa; Li, Chen; Habler, Gerlinde; Abart, Rainer

2017-04-01

When two neighbor phases are not in chemical equilibrium, they may react and produce a reaction rim at their interface, separating the mutually incompatible phases. At constant P-T-X conditions, such a reaction will continue until one of the reactants is completely consumed. Reaction rim growth involves transfer of chemical components across the growing rim by long-range diffusion and localized interface reactions on either side of the growing rim. Consequently, the thickness of the reaction rim will be a function of time. Yet, in order to quantify and interpret such corona structures and to define a reaction rate law, the kinetics and mechanism of rim formation must be well constrained. In particular, the coupling between long-range diffusion, and interface reaction must be known. In this contribution we focus on potential complexities associated with interface reactions. Many natural minerals contain inclusions of other phases, which in turn may influence the reaction interface propagation kinetics during host phase decomposition (Ashby et al. 1969), as a propagating reaction interface dissipates more free energy when bypassing a mineral inclusion, resulting in a locally decelerated reaction rate. Here, we report results of a SEM-STEM study of the interface between natural rutile-bearing corundum and a polycrystalline ferromagnesio-aluminate spinel that grew topotactically with respect to the corundum precursor as a consequence of its reaction with FeO and MgO from basaltic melt. Electron Backscatter Diffraction (EBSD) crystal orientation imaging revealed that the spinel rim is polycrystalline and exhibits (111) twinning that is parallel to the corundum (0001) plane. The rutile inclusions in corundum are elongated perpendicular to the corundum [0001] axis and are randomly oriented in the (0001) plane. Furthermore, they follow an oscillatory grain size distribution zonation with grain sizes being either a few tens of nanometers, or about 500 to 800 nanometers in

Synthesis and electrochemical study of Mg{sub 1.5}MnO{sub 3}: A defect spinel cathode for rechargeable magnesium battery

Energy Technology Data Exchange (ETDEWEB)

Saha, Partha [Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); US Department of Energy, National Energy Technology Laboratory, Morgantown, WV 26507 (United States); Jampani, Prashanth H., E-mail: pjampani@pitt.edu [Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); Hong, DaeHo [Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); Gattu, Bharat [Mechanical Engineering and Materials Science, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); Poston, James A.; Manivannan, Ayyakkannu [US Department of Energy, National Energy Technology Laboratory, Morgantown, WV 26507 (United States); Datta, Moni Kanchan [Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); US Department of Energy, National Energy Technology Laboratory, Morgantown, WV 26507 (United States); Kumta, Prashant N., E-mail: pkumta@pitt.edu [Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); US Department of Energy, National Energy Technology Laboratory, Morgantown, WV 26507 (United States); Mechanical Engineering and Materials Science, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); Chemical and Petroleum Engineering, Swanson School of Engineering, University of Pittsburgh, PA 15261 (United States); School of Dental Medicine, University of Pittsburgh, PA 15261 (United States); Center for Complex Engineered Multifunctional Materials, University of Pittsburgh, Pittsburgh, PA 15261 (United States)

2015-12-15

Graphical abstract: Mg{sub 1.5}MnO{sub 3}, a defect oxide spinel derived by the Pechini route, was tested as cathode for rechargeable magnesium battery. TEM and XRD analyses of Mg{sub 1.5}MnO{sub 3} shows the formation of ∼100 nm sized nano particles in the cubic defect spinel structure (space group: Fd3m; unit cell: 0.833294 nm). Cyclic voltammetry illustrates a reversible reaction occurring between 0.3 and 1.5 V versus magnesium. Galvanostatic cycling of the Mg{sub 1.5}MnO{sub 3} cathode exhibits a low capacity of ∼12.4 mAh/g up to 20 cycle with ∼99.9% Coulombic efficiency when cycled at a current rate of ∼C/27. XPS (X-ray photoelectron spectroscopy) surface probe of magnesiated/de-magnesiated electrodes confirm a change in the redox center of Mn-ions during intercalation/de-intercalation of Mg-ion from the Mg{sub 1.5}MnO{sub 3} electrode. The low capacity of Mg{sub 1.5}MnO{sub 3} electrode mainly stem from the kinetic limitation of Mg-ion removal from the defect oxide spinel as the electrochemical impedance spectroscopy results of electrodes after 1st and 2nd cycle show that charge transfer resistance, R{sub e}, increases post charge state whereas interfacial resistance, R{sub i}, increases after discharge state, respectively. - Highlights: • Pechini process yields 100 nm sized particles of the defect cubic spinel Mg{sub 1.5}MnO{sub 3}. • Stable capacity of ∼12.4 mAh/g obtained at C/27 rate and 99.9% Coulombic efficiency. • XPS shows change in valence state of Mn{sup 3+}/Mn{sup 4+} center with cycling. • Low capacity stems from increase in charge-transfer and interfacial resistances with cycling. - Abstract: Mg{sub 1.5}MnO{sub 3}, a defect oxide spinel (space group: Fd3m; unit cell: 0.833294 nm) of particle size ∼100 nm derived by the Pechini route was tested as a cathode for rechargeable magnesium battery. Cyclic voltammetry illustrates a reversible reaction occurring in the 0.3–2.0 V potential window versus magnesium. The spinel however

Progressive deformation of ultramafic rocks accompanied with deflection of layered structure and mylonitization culminating into a pseudotachylyte-bearing seismogenic fault - a field evidence of plastic instability

Science.gov (United States)

Ueda, T.; Obata, M.

2011-12-01

Plastic instability leading to rupture nucleation and propagetion (e.g. Hobbs et al.1986, Kelemen and Hirth, 2007) is an attractive hypothesis for deep earthquakes but lacked clear field evidences. 1D across-fault shear localization observed in some places (e.g. Jin et al.1998) is not clear if the deformation is directly related with seismicity. We present a clear field evidence of plastic instability as guided by pyroxenite/peridotite layering deflection structure (hereafter called LD structure, see figure) accompanied with mylonitization in spinel(Sp)-peridotite facies (P>~1GPa) in Balmuccia peridotite, Ivrea-Verbano Zone, Italy. The studied area contains abundant PST-bearing faults and N-S trending primary pyroxenite layers. Many faults in the area cut pyroxenite layers, but LD structure is found only in one place presented here. Many PSTs in the area have been (re)crystallized in Sp-peridotite facies, and have typically ultramylonitic texture (Ueda et al., 2008) with some injection veins. The fault with LD structure is situated in a fault system, which has two dominant attitudes with regional N-S extension. The shear strain of LD structure measured on outcrop surface is ~2.0. Near the fault, elongated Opx porphyroclasts (ellipses in figure) oblique to local layering are visible in peridotite. The dominant deformation textures are dynamic recrystallization in peridotite and kinking or undulatory extinction in pyroxenite. The mineral assemblages of the mylonite neoblast in the peridotite and the pyroxenite are Ol+Opx+Cpx+Sp+hornblende(Hbl), Cpx+Opx+Sp, respectively. Hbl typically occur only in neoblast. In the vicinity (several hundreds of micron) of the fault, dolomite(Dol) also occur in equilibrium with the assemblage above. The recrystallized grain sizes are 20-50 microns in peridotite and 10-30 microns in pyroxenite. The rarity of LD structure is consistent with general conception that deformation processes which lead to dynamic rupture initiation ought to be

Synthesis and characterization of advanced high capacity cathode active nanomaterials with three integrated spinel-layered phases for Li-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Bulut, Emrah, E-mail: ebulut@sakarya.edu.tr [Department of Chemistry, Sakarya University, 54187 Serdivan, Sakarya (Turkey); Can, Mustafa, E-mail: mstfacan@gmail.com [Vocational School of Arifiye, Sakarya University, 54580 Arifiye, Sakarya (Turkey); Özacar, Mahmut, E-mail: nmozacart@hotmail.com [Department of Chemistry, Sakarya University, 54187 Serdivan, Sakarya (Turkey); Akbulut, Hatem, E-mail: akbulut@Sakarya.edu.tr [Department of Metallurgical and Materials Engineering, Sakarya University, 54187 Serdivan, Sakarya (Turkey)

2016-06-15

Mesoporous cathode active materials that included undoped and separated Cu{sup 2+} and Co{sup 3+} doped spinels were prepared. The “doped spinel-Layered-Li-rich spinel” composite nanoparticles within the three integrated phased (LiM{sub 0,02}Mn{sub 1,98}O{sub 4}–Li{sub 2}MnO{sub 3}–Li{sub 1,27}Mn{sub 1,73}O{sub 4}; where M is Cu{sup 2+} and Co{sup 3+}) were synthesized by a microwave assisted hydrothermal synthesis. These materials were investigated with X-Ray powder Diffraction spectroscopy (XRD), Scanning Electron Microscopy (SEM and FE-SEM), High Resolution Transmission Electron Microscopy (HR-TEM), galvanostatic cycling at 0.1C and 0.5C rates, Cyclic Voltammetry (CV), and Electrochemical Impedance Spectroscopy (EIS). The effects of the calcination temperature and the partial substitution of Mn{sup 3+} in the spinel by Cu{sup 2+} and Co{sup 3+}, and onto the spinel structure were investigated with XRD. The lattice parameters of the spinel structured compounds were calculated from the XRD data using the Williamson-Hall equation. However, the morphological changes, which depended on the calcination temperature, were examined by SEM, FE-SEM and HRTEM. Furthermore, the two other phases which were different from LiM{sub 0,02}Mn{sub 1,98}O{sub 4} had a great impact on the electrochemical performance over the potential range of the 3–5 V. At the 0.1C rate, the first discharge capacities of undoped and Cu{sup 2+}, Co{sup 3+} doped materials were 577, 285, 560 mAh/g respectively. After 50 cycles at 0.5C rate, we achieved 96.2%; 52.5%; 95.4% capacity retention for the undoped and Cu{sup 2+}, Co{sup 3+} doped materials respectively. - Highlights: • Mesoporous cathode active nanomaterials with three integrated phase were synthesized. • The materials were characterized structurally by XRD, FE-SEM, HR-TEM. • Integrated phases provide an additional 400 mAh/g discharge capacity at low rate. • Higher specific capacities than literature values were achieved at 0

Petrology of Ortsog-Uul peridotite-gabbro massif in Western Mongolia

Science.gov (United States)

Shapovalova, M.; Tolstykh, N.; Shelepaev, R.; Cherdantseva, M.

2017-12-01

The Ortsog-Uul mafic-ultramafic massif of Western Mongolia is located in a tectonic block with overturned bedding. The massif hosts two intrusions: a rhythmically-layered peridotite-gabbro association (Intrusion 1) and massive Bt-bearing amphibole-olivine gabbro (Intrusion 2). Intrusions 1 and 2 have different petrology features. Early Intrusion 1 (278±2.5Ma) is characterized by lower concentrations of alkalis, titanium and phosphorus than late Intrusion 2 (272±2Ma). The chondrite-normalized REE and primitive mantle-normalized rare elements patterns of Ortsog-Uul intrusions have similar curves of elements distribution. However, Intrusion 2 is characterized higher contents of REE and rare elements. High concentrations of incompatible elements are indicative of strong fractionation process. It has been suggested that Intrusions 1 and 2 derived from compositionally different parental melts. Model calculations (COMAGMAT-3.57) show that parental melts of two intrusions were close to high-Mg picrobasaltic magmas. The concentration of MgO in melt is 16.21 (Intrusion 1) and 16.17 (Intrusion 2). Isotopic data of Ortsog-Uul magmatic rocks exhibit different values of εNd (positive and negative) for Intrusion 1 and 2, respectively.

Associated chemical and carbon isotopic composition variations in diamonds from Finsch and Premier kimberlite, South Africa

International Nuclear Information System (INIS)

Deines, P.

1984-01-01

The carbon isotopic composition of 66 inclusion-containing diamonds from the Premier kimberlite, South Africa, 93 inclusion-containing diamonds and four diamonds of two diamond-bearing peridotite xenoliths from the Finsch kimberlite, South Africa was measured. The data suggest a relationship between the carbon isotopic composition of the diamonds and the chemical composition of the associated silicates. For both kimberlites similar trends are noted for diamonds containing peridotite-suite inclusions (P-type) and for diamonds containing eclogite-suite inclusions (E-type): Higher delta 13 C P-type diamonds tend to have inclusions lower in SiO 2 , Al 2 O 3 , Cr 2 O 3 , MgO, Mg/(Mg + Fe) and higher in FeO and CaO. Higher delta 13 C E-type diamonds tend to have inclusions lower in SiO 2 , Al 2 O 3 , MgO, Mg/(Mg + Fe), Na 2 O, K 2 O, TiO 2 and higher in CaO, Ca/(Ca + Mg). Consideration of a number of different models that have been proposed for the genesis of kimberlites, their zenoliths and diamonds shows that they are all consistent with the conclusion that in the mantle, regions exist that are characterized by different mean carbon isotopic compositions. (author)

Lithium-deficient Li YMn2O4 spinels (0.9 ≤ Y < 1): Lithium content, synthesis temperature, thermal behaviour and electrochemical properties

International Nuclear Information System (INIS)

Pascual, Laura; Perez-Revenga, M. Luz; Rojas, Rosa M.; Rojo, Jose M.; Amarilla, J. Manuel

2006-01-01

Lithium-deficient Li Y Mn 2 O 4 spinels (LD-Li Y Mn 2 O 4 ) with nominal composition (0.9 ≤ Y 2 O 3 and LiNO 3 at temperatures ranging from 700 deg. C to 850 deg. C. X-ray diffraction data show that LD-Li Y Mn 2 O 4 spinels are obtained as single phases in the range Y = 0.975-1 at 700 deg. C and 750 deg. C. Morphological characterization by transmission electron microscopy shows that the particle size of LD-Li Y Mn 2 O 4 spinels increases on decreasing the Li-content. The influence of the Li-content and the synthesis temperature on the thermal and electrochemical behaviours has been systematically studied. Thermal analysis studies indicate that the temperature of the first thermal effect in the differential thermal analysis (DTA)/thermogravimetric (TG) curves, T C1 , linearly increases on decreasing the Li-content. The electrochemical properties of LD-Li Y Mn 2 O 4 spinels, determined by galvanostatic cycling, notably change with the synthesis conditions. So, the first discharge capacity, Q disch. , at C rate increases on rising the Li-content and the synthesis temperature. The sample Li 0.975 Mn 2 O 4 synthesized at 700 deg. C has a Q disch. = 123 mAh g -1 and a capacity retention of 99.77% per cycle. This LD-Li Y Mn 2 O 4 sample had the best electrochemical characteristics of the series

Petrogenesis of the Alaskan-type mafic-ultramafic complex in the Makkah quadrangle, western Arabian Shield, Saudi Arabia

Science.gov (United States)

Habtoor, Abdelmonem; Ahmed, Ahmed Hassan; Harbi, Hesham

2016-10-01

The Makkah quadrangle is a part of the Jeddah terrane in the Precambrian basement, Western Arabian Shield of Saudi Arabia. Gabal Taftafan mafic-ultramafic complex lies within the central part of the Makkah quadrangle. The Taftafan mafic-ultramafic complex is a well-differentiated rock association which comprises of dunite core, hornblende- and plagioclase-bearing peridotites, troctolite, clinopyroxenite and marginal gabbro, in a distinctive zonal structure. The bulk-rock geochemistry of the Taftafan mafic-ultramafic rocks is characterized by a tholeiitic/sub-alkaline affinity with high Mg in the ultramafic core (0.84) and is systematically decreased towards the marginal gabbro (0.60). The patterns of trace elements show enrichment in the fluid-mobile elements (Sr, Ba) and a pronounced negative Nb anomaly which reflect a hydrous parental magma generated in a subduction tectonic setting. The mafic-ultramafic rocks of the Taftafan complex have low total rare earth elements (REE) displaying sub-parallel patterns leading to the assumption that these rocks are comagmatic and are formed by fractional crystallization from a common magma type. The platinum-group elements (PGE) content of all rock types in the Taftafan complex is very low, with ∑ PPGE > ∑ IPGE; displaying slightly positive slopes of the PGE distribution patterns. The chemistry of ferromagnesian minerals is characterized by a high forsterite (Fo) olivine with wide range (Fo91-67), from ultramafic core to the marginal gabbro, Ca-rich diopsidic clinopyroxene, and calcic hornblende. Orthopyroxene is almost absent from all rock types, or very rare when present. Hornblende and Ca-plagioclase possess the longest crystallization history since they are present in almost all rock types of the complex. Spinels in the dunite and hornblende-bearing peridotite core show homogeneous composition with intermediate Cr# (0.53-0.67). Plagioclase-bearing peridotite and troctolite have two exsolved types of spinel; Al

Inclusions in diamonds constrain thermo-chemical conditions during Mesozoic metasomatism of the Kaapvaal cratonic mantle

Science.gov (United States)

Weiss, Yaakov; Navon, Oded; Goldstein, Steven L.; Harris, Jeff W.

2018-06-01

Fluid/melt inclusions in diamonds, which were encapsulated during a metasomatic event and over a short period of time, are isolated from their surrounding mantle, offering the opportunity to constrain changes in the sub-continental lithospheric mantle (SCLM) that occurred during individual thermo-chemical events, as well as the composition of the fluids involved and their sources. We have analyzed a suite of 8 microinclusion-bearing diamonds from the Group I De Beers Pool kimberlites, South Africa, using FTIR, EPMA and LA-ICP-MS. Seven of the diamonds trapped incompatible-element-enriched saline high density fluids (HDFs), carry peridotitic mineral microinclusions, and substitutional nitrogen almost exclusively in A-centers. This low-aggregation state of nitrogen indicates a short mantle residence times and/or low mantle ambient temperature for these diamonds. A short residence time is favored because, elevated thermal conditions prevailed in the South African lithosphere during and following the Karoo flood basalt volcanism at ∼180 Ma, thus the saline metasomatism must have occurred close to the time of kimberlite eruptions at ∼85 Ma. Another diamond encapsulated incompatible-element-enriched silicic HDFs and has 25% of its nitrogen content residing in B-centers, implying formation during an earlier and different metasomatic event that likely relates to the Karoo magmatism at ca. 180 Ma. Thermometry of mineral microinclusions in the diamonds carrying saline HDFs, based on Mg-Fe exchange between garnet-orthopyroxene (Opx)/clinopyroxene (Cpx)/olivine and the Opx-Cpx thermometer, yield temperatures between 875-1080 °C at 5 GPa. These temperatures overlap with conditions recorded by touching inclusion pairs in diamonds from the De Beers Pool kimberlites, which represent the mantle ambient conditions just before eruption, and are altogether lower by 150-250 °C compared to P-T gradients recorded by peridotite xenoliths from the same locality. Oxygen fugacity (fO2

Synthesis and electrochemical characteristics of spinel LiMn2O4 via a precipitation spray-drying process

International Nuclear Information System (INIS)

Wu, H.M.; Tu, J.P.; Yuan, Y.F.; Li, Y.; Zhao, X.B.; Cao, G.S.

2005-01-01

Spinel LiMn 2 O 4 has been successfully synthesized using a precipitation spray-drying process. After the precursor was annealed at 750 deg. C for 10 h, the synthesized material was well-crystallized spinel particle, and exhibited uniform particle size distribution. From cyclic voltammetry results, there is an anomalous redox peaks (3.75/3.26 V). In the charge/discharge potential (versus Li) ranging from 3.2 to 4.5 V, it delivered a high initial discharge capacity of 123 mAh/g at a discharge rate of 60 μA/cm 2 (1/4 C rate). At a high discharge rate of 2.4 mA/cm 2 (10 C rate), the obtainable reversible capacity was 79 mAh/g. The simple procedure of precipitation spray-drying process is time and energy saving, and thus is promising for commercial application

FC and ZFC magnetic properties of ferro-spinels (MFe2O4) prepared by solution-combustion method

Science.gov (United States)

Aravind, G.; Kumar, R. Vijaya; Nathaniyal, V.; Rambabu, T.; Ravinder, D.

2017-07-01

Magnetic ferro-spinels MFe2O4 (M= Co and Ni) prepared by citrate-gel solution combustion method using metal nitrates with low sintering temperature (500°C). From the XRD and TEM studies confirm that a nano crystalline nature of the prepared samples. Field Cooled (FC) and Zero Field Cooled (ZFC) magnetic studies of the prepared ferro-spinels are measured by using vibrating sample magnetometer (VSM). The resultant magnetization of the prepared samples as a function of an applied magnetic field 10 T was measured at two different temperatures 5 K and 310 K. Field Cooled (FC) and Zero Field Cooled (ZFC) magnetization measurements under an applied field of 100 Oe and 1000 Oe in the temperature range of 5-375 K were carried out, which shows the blocking temperature of these two samples at around 350 K.

Synthesis of high-surface-area spinel-type MgAl2O4 nanoparticles ...

Indian Academy of Sciences (India)

Home; Journals; Bulletin of Materials Science; Volume 40; Issue 1. Synthesis of high-surface-area spinel-type MgAl 2 O 4 nanoparticles by [Al(sal) 2 (H 2 O) 2 ] 2 [Mg(dipic) 2 ] and [Mg(H 2 O) 6 ][Al(ox) 2 (H 2 O) 2 ] 2 ·5H 2 O: influence of inorganic precursor type. Volume 40 Issue 1 February 2017 pp 45-53 ...

Long term in vivo imaging with Cr{sup 3+} doped spinel nanoparticles exhibiting persistent luminescence

Energy Technology Data Exchange (ETDEWEB)

Viana, B., E-mail: bruno.viana@chimie-paristech.fr [PSL Research University, Chimie ParisTech−CNRS, Institut de Recherche de Chimie Paris, 75005 Paris (France); Chimie-ParisTech, Paris cedex F-75231 (France); Sharma, S.K.; Gourier, D. [PSL Research University, Chimie ParisTech−CNRS, Institut de Recherche de Chimie Paris, 75005 Paris (France); Chimie-ParisTech, Paris cedex F-75231 (France); Maldiney, T.; Teston, E.; Scherman, D. [Unité de Technologies Chimiques et Biologiques pour la Santé (UTCBS), CNRS UMR 8258, INSERM U 1022, Paris cedex F-75270 (France); Université Paris Descartes, Sorbonne Paris Cité, Faculté des Sciences Pharmaceutiques et Biologiques, Paris cedex F-75270 (France); Chimie-ParisTech, Paris cedex F-75231 (France); Richard, C., E-mail: cyrille.richard@parisdescartes.fr [Unité de Technologies Chimiques et Biologiques pour la Santé (UTCBS), CNRS UMR 8258, INSERM U 1022, Paris cedex F-75270 (France); Université Paris Descartes, Sorbonne Paris Cité, Faculté des Sciences Pharmaceutiques et Biologiques, Paris cedex F-75270 (France); Chimie-ParisTech, Paris cedex F-75231 (France)

2016-02-15

Persistent luminescence is a singular property of some materials which are able to store the excitation or light irradiation energy at intrinsic traps or defects before slowly emitting lower energy photons within several hours. When such compounds are prepared as nanoparticles (NPs), when functionalization is realized to get colloidal materials well dispersed in aqueous medium, such nanoprobes open the use of the persistent luminescence for bioimaging applications. Recently, the numbers of in vivo applications increased with new modalities and new expectations. In this review, we focused our attention on the ZnGa{sub 2}O{sub 4}:Cr (ZGO:Cr) nanoparticles. When ZnGa{sub 2}O{sub 4} (ZGO), a normal spinel is doped with Cr{sup 3+} ions, a high brightness persistent luminescence material with an emission spectrum perfectly matching the transparency window of living tissues is obtained. It allows in vivo mouse imaging with an excellent target-to-background ratio. One interesting characteristic of ZGO:Cr lies in the fact that its persistent luminescence can be excited with orange/red light, well below its band gap energy and in the transparency window of living tissues. This important property allows multiple re-excitations to perform long term bioimaging. Antisite defects of the direct spinel structure are assumed to provide shallow traps which store the excitation light. Charge release by room temperature thermal excitation and recombination center, here trivalent chromium, are responsible for the persistent luminescence. Following a primary excitation (UV or visible), one also observed that trapped charges can be released under 977 nm light stimulation for several spinel gallate materials, therefore increasing the modalities and the materials envisioned for in vivo excitation of these NPs. - Highlights: • Review of the persistent luminescence for bio-imaging. • Long term bioimaging by in vivo excitation and photostimulation. • Challenges and main advances in the

Dislocation loops in spinel crystals irradiated successively with deep and shallow ion implants

International Nuclear Information System (INIS)

Ai, R.X.; Cooper, E.A.; Sickafus, K.E.; Nastasi, M.; Bordes, N.; Ewing, R.C.

1993-01-01

This study examines the influence of microstructural defects on irradiation damage accumulation in the oxide spinel. Single crystals of the compound MgAl 2 O 4 with surface normal [111] were irradiated under cryogenic temperature (100K) either with 50 keV Ne ions (fluence 5.0 x 10 12 /cm 2 ), 400 keV Ne ions (fluence 6.7 x 10 13 /cm 2 ) or successively with 400 keV Ne ions followed by 50 keV Ne ions. The projected range of 50 keV Ne ions in spinel is ∼50 mn (''shallow'') while the projected range of 400 keV Ne ions is ∼500 mn (''deep''). Transmission electron microscopy (TEM) was used to examine dislocation loops/defect clusters formed by the implantation process. Measurements of the dislocation loop size were made using weak-beam imaging technique on cross-sectional TEM ion-implanted specimens. Defect clusters were observed in both deep and shallow implanted specimens, while dislocation loops were observed in the shallow implanted sample that was previously irradiated by 400 keV Ne ions. Cluster size was seen to increase for shallow implants in crystals irradiated with a deep implant (size ∼8.5 nm) as compared to crystals treated only to a shallow implant (size ∼3.1 nm)

Depletion, cryptic metasomatism, and modal metasomatism (refertilization) of Variscan lithospheric mantle: Evidence from major elements, trace elements, and Sr-Nd-Os isotopes in a Saxothuringian garnet peridotite

Czech Academy of Sciences Publication Activity Database

Medaris Jr., L. G.; Ackerman, Lukáš; Jelínek, E.; Michels, Z. D.; Erban, V.; Kotková, J.

2015-01-01

Roč. 226, SI (2015), s. 81-97 ISSN 0024-4937 Institutional support: RVO:67985831 Keywords : garnet peridotite * Variscan * Bohemian Massif * Sr-Nd-Os isotopes * depletion cryptic metasomatism and refertilization * P-T conditions Subject RIV: DD - Geochemistry Impact factor: 3.723, year: 2015

Experimental Determination of Spinel/Melt, Olivine/Melt, and Pyroxene/Melt Partition Coefficients for Re, Ru, Pd, Au, and Pt

Science.gov (United States)

Righter, K.; Campbell, A. J.; Humayun, M.

2003-01-01

Experimental studies have identified spinels as important hosts phases for many of the highly siderophile elements (HSE). Yet experimental studies involving chromite or Cr-rich spinel have been lacking. Experimental studies of partitioning of HSEs between silicate, oxides and silicate melt are plagued by low solubilities and the presence of small metallic nuggets at oxygen fugacities relevant to magmas, which interfere with analysis of the phases of interest. We have circumvented these problems in two ways: 1) performing experiments at oxidized conditions, which are still relevant to natural systems but in which nuggets are not observed, and 2) analysis of run products with laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), allowing a combination of high sensitivity and good spatial resolution.

Structural modifications of spinels under radiation

International Nuclear Information System (INIS)

Quentin, A.

2010-12-01

This work is devoted to the study of spinel structure materials under radiation. For that purpose, samples of polycrystalline ZnAl 2 O 4 and monocrystalline MgAl 2 O 4 were irradiated by different heavy ions with different energies. Samples of ZnAl 2 O 4 were studied par electron transmission microscopy, and by grazing incidence X-Ray diffraction and Rietveld analysis. Samples of MgAl 2 O 4 were studied by optical spectroscopy. Most of the results concern amorphization and crystalline structure modification of ZnAl 2 O 4 especially the inversion. We were able to determine a stopping power threshold for amorphization, between 11 keV/nm and 12 keV/nm, and also the amorphization process, which is a multiple impacts process. We studied the evolution of the amorphous phase by TEM and showed a nano-patterning phenomenon. Concerning the inversion, we determined that it did happen by a single impact process, and the saturation value did not reach the random cation distribution value. Inversion and amorphization have different, but close, stopping power threshold. However, amorphization seems to be conditioned by a pre-damage of the material which consists in inversion. (author)

Studies on densification, mechanical, micro-structural and structure–properties relationship of magnesium aluminate spinel refractory aggregates prepared from Indian magnesite

International Nuclear Information System (INIS)

Ghosh, Chandrima; Ghosh, Arup; Haldar, Manas Kamal

2015-01-01

The present work intends to study the development of magnesium aluminate spinel aggregates from Indian magnesite in a single firing stage. The raw magnesite has been evaluated in terms of chemical analysis, differential thermal analysis, thermogravimetric analysis, infrared spectroscopy, and X-ray diffraction. The experimental batch containing Indian magnesite and calcined alumina has been sintered in the temperature range of 1550 °C–1700 °C. The sintered material has been characterized in terms of physico-chemical properties like bulk density, apparent porosity, true density, relative density and thermo-mechanical/mechanical properties like hot modulus of rupture, thermal shock resistance, cold modulus of rupture and structural properties by X-ray diffraction in terms of phase identification and evaluation of crystal structure parameters of corresponding phases by Rietveld analysis. The microstructures developed at different temperatures have been analyzed by field emission scanning electron microscope study and compositional analysis of the developed phase has been carried out by energy dispersive X-ray study. - Highlights: • The studies have been done to characterize the developed magnesium aluminate spinel. • The studies reveal correlation between refractory behavior of spinel and developed microstructures. • The studies show the values of lattice parameters of developed phases

Defect kinetics in spinels: Long-time simulations of MgAl2O4, MgGa2O4, and MgIn2O4

International Nuclear Information System (INIS)

Uberuaga, B. P.; Voter, A. F.; Sickafus, K. E.; Bacorisen, D.; Smith, Roger; Ball, J. A.; Grimes, R. W.

2007-01-01

Building upon work in which we examined defect production and stability in spinels, we now turn to defect kinetics. Using temperature accelerated dynamics (TAD), we characterize the kinetics of defects in three spinel oxides: magnesium aluminate MgAl 2 O 4 , magnesium gallate MgGa 2 O 4 , and magnesium indate MgIn 2 O 4 . These materials have varying tendencies to disorder on the cation sublattices. In order to understand chemical composition effects, we first examine defect kinetics in perfectly ordered, or normal, spinels, focusing on point defects on each sublattice. We then examine the role that cation disorder has on defect mobility. Using TAD, we find that disorder creates local environments which strongly trap point defects, effectively reducing their mobility. We explore the consequences of this trapping via kinetic Monte Carlo (KMC) simulations on the oxygen vacancy (V O ) in MgGa 2 O 4 , finding that V O mobility is directly related to the degree of inversion in the system

X-ray diffraction at high pressure and high/low temperatures using synchrotron radiation. Applications in the study of spinel structures

International Nuclear Information System (INIS)

Gerward, L.; Jiang, J.Z.; Olsen, J.S.; Recio, J.M.; Wakowska, A.

2004-01-01

High-pressure x-ray diffraction made a quantum leap in the 1960's with the advent of the diamond-anvil cell. This ingenious device, where two opposing diamond faces apply pressure to a tiny sample, made it possible to replicate the pressure near the core of the Earth by turning a thumbscrew. Multianvil cells, such as the Japanese MAX80 press, were developed for combined high-pressure and high-temperature studies. The availability n at about the same time n of dedicated synchrotron radiation sources of hard x-rays was another big step forward. Since then, the white-beam energy-dispersive method has been the workhorse for high pressure, high-temperature x-ray diffraction, although it is now gradually being replaced by high-resolution monochromatic methods based on the image plate, the CCD camera or other electronic area detectors. The first part of the paper is a review of high-pressure x-ray diffraction (HPXRD), covering roughly the last three decades. Physical parameters, such as the bulk modulus, the compressibility and the equation of state, are defined. The diamond-anvil cell, the multianvil press and other high-pressure devices are described, as well as synchrotron radiation sources and recording techniques. Examples are drawn from current experimental and theoretical research on crystal structures of the spinel type. Accurate structural parameters have been determined at ambient conditions and at low temperatures using single-crystal diffraction and four-circle diffractometers. The uniform high-pressure behavior of the oxide spinels has been investigated in detail and compared with the corresponding behavior of selenium-based spinels. The synthesis of advanced novel materials is exemplified in the case of the cubic spinel Si 3 N 4 . This and other nitrogen spinels, which have a bulk modulus of about 300 GPa modulated by the actual cation, are opening a road towards superhard materials. The paper finishes off with an outlook into the future, where new

Rietveld structure refinement and elastic properties of MgAlxCrxFe2-2xO4 spinel ferrites

Science.gov (United States)

Thummer, K. P.; Tanna, Ashish R.; Joshi, Hiren H.

2017-05-01

MgAlxCrxFe2-2xO4 (x = 0.1, 03 & 0.6) ferrites are synthesized by solid state reaction method. The Rietveld refinement of X-ray diffraction (XRD) data confirms the cubic spinel structure with Fd3m space group. The Fourier Transform Infrared Transmission Spectroscopy (FTIR) is employed to study elastic properties of present systems at 300K. The force constants for tetrahedral (A) and octahedral (B) sites of the spinel lattice are determined by infrared spectral and X-ray diffraction analysis. The elastic constants like bulk modulus, rigidity modulus, Young's modulus, Poisson's ratio and Debye temperature are determined. The vibrational frequency of both the interstitial sites increases as Al-Cr content increases hence the force constant and elastic moduli for all the samples are found to increase for the present ferrite system.

Modification of an ancient subcontinental lithospheric mantle by continental subduction: Insight from the Maowu garnet peridotites in the Dabie UHP belt, eastern China

Science.gov (United States)

Chen, Yi; Su, Bin; Chu, Zhuyin

2017-05-01

Orogenic mantle-derived peridotites commonly originate from the subcontinental lithospheric mantle (SCLM) and thus provide a key target to investigate the modification of the SCLM by a subducting slab. The Maowu ultramafic rocks from the Dabie ultrahigh-pressure (UHP) metamorphic belt have formerly been debated as representing cumulates or mantle-derived peridotites. Detailed petrological and geochemical data presented in this study provide new constraints on the origin and formation of the peridotites involving melt depletion in the ancient SCLM and deep crustal metasomatism. The Maowu garnet dunites have refractory bulk compositions characterized by high Mg# (91.9-92.0) and Ni (2537-2892 ppm) values and low Al2O3 (0.26-0.76 wt.%), CaO (0.05-0.32 wt.%), TiO2 (China craton. Many garnet orthopyroxenite veins crosscutting the Maowu dunites preserve abundant metasomatic textures and show variable enrichment in incompatible elements. Mineral and whole-rock chemistry indicate that these veins represent metasomatic products between the wall dunites and silica-rich hydrous melts under UHP conditions. The veins show large variations in platinum-group element (PGE) signatures and Re-Os isotopes. The garnet-poor orthopyroxenite veins are characterized by low Al2O3 ( 6 wt.%) and S (99-306 ppm) contents and show melt-like PGE patterns and high 187Os/188Os ratios (up to 0.36910). These features, combined with the occurrence of interstitial sulfides in the garnet-rich orthopyroxenite veins, suggest that crust-derived sulfur-saturated silicate melts may have significantly modified the PGE signature and destroyed the Re-Os systematics of the SCLM. However, when the crust-derived silicate melts became sulfur-depleted, such melts would not significantly modify the PGE patterns, radiogenic Os-isotope compositions or the Re-depletion model ages of the SCLM. Consequently, deep crust-mantle interactions in continental subduction zones could induce high degrees of Os isotopic

Controls on the rheological properties of peridotite at a palaeosubduction interface: A transect across the base of the Oman-UAE ophiolite

Science.gov (United States)

Ambrose, Tyler K.; Wallis, David; Hansen, Lars N.; Waters, Dave J.; Searle, Michael P.

2018-06-01

Studies of experimentally deformed rocks and small-scale natural shear zones have demonstrated that volumetrically minor phases can control strain localisation by limiting grain growth and promoting grain-size sensitive deformation mechanisms. These small-scale studies are often used to infer a critical role for minor phases in the development of plate boundaries. However, the role of minor phases in strain localisation at an actual plate boundary remains to be tested by direct observation. In order to test the hypothesis that minor phases control strain localisation at plate boundaries, we conducted microstructural analyses of peridotite samples collected along a ∼1 km transect across the base of the Oman-United Arab Emirates (UAE) ophiolite. The base of the ophiolite is marked by the Semail thrust, which represents the now exhumed contact between subducted oceanic crust and the overlying mantle wedge. As such, the base of the ophiolite provides the opportunity to directly examine a former plate boundary. Our results demonstrate that the mean olivine grain size is inversely proportional to the abundance of minor phases (primarily orthopyroxene, as well as clinopyroxene, hornblende, and spinel), consistent with suppression of grain growth by grain-boundary pinning. Our results also reveal that mean olivine grain size is proportional to CPO strength (both of which generally decrease towards the metamorphic sole), suggesting that the fraction of strain produced by different deformation mechanisms varied spatially. Experimentally-derived flow laws indicate that under the inferred deformation conditions, the viscosity of olivine was grain-size sensitive. As such, grain size, and thereby the abundance of minor phases, influenced viscosity during subduction-related deformation along the base of the mantle wedge. We calculate an order of magnitude decrease in the viscosity of olivine towards the base of the ophiolite, which suggests strain was localised near the

Some Spinel Oxide Compounds as Reducing Gas Sensors

Directory of Open Access Journals (Sweden)

Nicolae Rezlescu

2007-04-01

Full Text Available Four spinel ferrites, MFe2O4 (M = Cu, Cd, Zn and Ni, having various grain sizes (100 – 700 nm were prepared by sol-gel-selfcombustion and their sensing properties to reducing gases were investigated. The gas sensing characteristics were obtained by measuring the sensitivity as a function of various controlling factors, like operating temperature, composition and concentration of the gas, and finally the response time. The sensitivity of four ferrites to reducing gases like acetone, ethanol and LPG was been compared. It was revealed that CuFe2O4 is the most sensitive to LPG and ZnFe2O4 can be used as a sensor to selectively detect ethanol vapors in air. The strong interaction between ethanol and porous ZnFe2O4 can explain the selective sensitivity to ethanol and negligible sensitivity to the other reducing gases.

Chemical synthesis of nickel ferrite spinel designed as an insulating bilayer coating on ferromagnetic particles

Czech Academy of Sciences Publication Activity Database

Strečková, M.; Hadraba, Hynek; Bureš, R.; Fáberová, M.; Roupcová, Pavla; Kuběna, Ivo; Medvecký, L.; Girman, V.; Kollár, P.; Füzer, J.; Čižmár, E.

2015-01-01

Roč. 270, MAY (2015), s. 66-76 ISSN 0257-8972 R&D Projects: GA ČR(CZ) GA14-25246S; GA MŠk(CZ) ED1.1.00/02.0068 Institutional support: RVO:68081723 Keywords : soft magnetic composite * NiFe2O4 spinel ferrite * coating * precipitation method * focused ion beam Subject RIV: JG - Metallurgy Impact factor: 2.139, year: 2015

Implications of Zn/Fe ratios for the sources of Colorado Plateau basalts

Science.gov (United States)

Rudzitis, S.; Reid, M. R.

2011-12-01

Early Miocene to recent mafic magmatism migrated across the Arizona Transition Zone towards the center of the stable Colorado Plateau at a rate of ~ 3-6 km/Myr (Roy et al., 2009). Present-day volcanic centers are close to a stepwise change in the thickness of the lithosphere between the Colorado Plateau and Basin and Range. Accordingly, volcanic migration might track progressive thinning of the lithosphere towards the center of the Colorado Plateau. This project aims to determine the conditions of melt generation across the transition zone in order to investigate the temporal/spatial correlation between volcanism and thinning of the Colorado Plateau lithosphere. Pressure and temperature estimates for Colorado Plateau basalts can be obtained from the Mg and Si contents of melts (Lee et al, 2009) but require melting of a peridotitic source. Eclogite and pyroxenite xenoliths reported in Colorado Plateau basalts show that melt sources could be olivine-poor. Zn/Fe ratios in melts can help to distinguish contributions from olivine-poor sources because they are sensitive to differences in bulk chemistry and to mineralogy (Le Roux et al., 2010). Specifically, Zn/Fe is not fractionated between melt, olivine, and orthopyroxene, but is highly fractionated when clinopyroxene and garnet are present. Our work to date has focused on laser ablation-IC-PMS analysis of individual olivine grains from high-Mg basalts (>8.0 wt. %) from the San Francisco and Mormon Mountain volcanic fields. Preliminary values of Zn/Fe ratios that represent the averages of multiple analyses of several grains in individual samples range from 7.9 to 9.3 (x10000). Variations of up to 1.7 (x10000) in the ratios exist between individual grains within samples and could be the result of co-crystallization of clinopyroxene with olivine. The lowest values in each sample should approach the Zn/Fe ratios of parental melts, and are, in turn, similar to MORB values and predicted peridotite melts. The results suggest

First-principle investigation on stability of Co-doped spinel λ-Mn4-xCoxO8

Institute of Scientific and Technical Information of China (English)

HUANG Ke-long; CHEN Chun-an; LIU Su-qin; LUO Qiong; LIU Zhi-guo

2007-01-01

The mechanism of stability of Co-doped spinel λ-MnO2 that is referred to as spinel LiχMn2O4 (χ=0) was studied by using the first-principle calculation method. The total energy and formation enthalpy can be decreased remarkably due to the Co substation,resulting in a more stable structure of λ-MnχCr2-χO4. The bond order and DOS analysis were given in detail to explain the nature of stability improvement. The calculated results show that as the content of Co dopant increases, the bond order of Mn-O becomes larger and the peak of density of states around Fermi level shifts toward lower energy. The charge density distribution illustrates that the Mn-O bonding is ionic and partially covalent, and the covalent Mn-O bonding becomes stronger with the increase of Co dopant content. The results confirm that the Co-doping will enhance the stability of λ-MnO2 and hence improve the electrochemistry performance of LiχMn2O4.

Asthenospheric percolation of alkaline melts beneath the St. Paul region (Central Atlantic Ocean)

Science.gov (United States)

Brunelli, Daniele; Seyler, Monique

2010-01-01

Two peridotite suites collected by submersible in the equatorial Atlantic Ocean (Hekinian et al., 2000) were studied for textures, modes, and in situ major and trace element compositions in pyroxenes. Dive SP12 runs along the immersed flank of the St. Peter and Paul Rocks islets where amphibole-bearing, ultramafic mylonites enriched in alkalies and incompatible elements are exposed (Roden et al., 1984), whereas dive SP03 sampled a small intra-transform spreading centre situated about 370 km east of the St. Peter and Paul Rocks. Both suites are characterized by undeformed, coarse-grained granular textures typical of abyssal peridotites, derived from residual mantle after ˜ 15% melting of a DMM source, starting in the garnet stability field. Trace element modelling, textures and lack of mineral zoning indicate that the residual peridotites were percolated, reacted and refertilized by ˜ 2.6% partially aggregated melts in the uppermost level of the melting region. This relatively large amount of refertilization is in agreement with the cold and thick lithosphere inferred by previous studies. Freezing of trapped melts occurred as the peridotite entered the conductive layer, resulting in late-stage crystallization of olivine, clinopyroxene, spinel, ± plagioclase. Chondrite-normalized REE patterns in clinopyroxenes from SP03 indicate that they last equilibrated with (ultra-) depleted partial melts. In contrast, REE concentrations in clinopyroxenes from SP12 display U and S shaped LREE-enriched patterns and the calculated compositions of the impregnating melts span the compositional range of the regional basalts, which vary from normal MORB to alkali basalt sometimes modified by chromatographic fractionation with no, or very limited, mineral reaction. Thus the mylonitic band forming the St. Peter and St. Paul Rocks ridge is not a fragment of subcontinental lithospheric mantle left behind during the opening of the Central Atlantic, nor the source of the alkaline basalts

The Effects of Oxygen Partial Pressure on Liquidus Temperature of a High-Level Waste Glass with Spinel as the Primary Phase

International Nuclear Information System (INIS)

Izak, Pavel; Hrma, Pavel R.; Wilson, Benjamin K.; Vienna, John D.

2000-01-01

The redox state of iron affects spinal crystallization in vitrified high-level waste (HLW) glass. Simulated HLW glass with spinel as the primary crystalline phase field was heat treated at constant temperatures within the interval from 850 C to 1300 C under varying atmospheres with oxygen partial pressure, Po2, ranging from 1x10-16 kPa (pure CO) to 101 kPa (pure O2). Liquidus temperature (TL) of glass increased with decreasing Po2 up to Po2 > 3 x 10-9 kPa. At Po2 < 3 x 10-9 kPa, Ni-Fe alloy precipitated from the glass, and TL decreased. Samples were analyzed with optical microscope and scanning electron microscope. The mass fraction of spinel in glass was determined using quantitative X-ray diffraction. Spinel composition was investigated with energy disperse spectroscopy. Ferrous-ferric equilibrium at TL was calculated in a HLW glass as a function of temperature and Po2, based on the previous studies by Schreiber. TL/FeO over the interval 0.0063 < gFeO < 0.051 (1x10-2 kPa < Po2 < 3x10-9 kPa) was estimated from calculated ferrous-ferric equilibrium at TL as 1835 C

Activity of Aniline Methylation over Fe-Cu-Cr Ternary Spinel Systems

Directory of Open Access Journals (Sweden)

Reni George

2014-03-01

Full Text Available A series of spinels having thegeneral formula CuCr2-xFexO4 with x=0.25,0.75, 1.25, 1.75 were prepared by co-precipitation method. The catalysts werecharacterized by various physico-chemical methods like XRD, BET, UV-DRS, SEM,EDX, TPD etc. The reaction of aniline with methanol was studied in a fixed-bedreactor system as a potential source for the production of various methylanilines. It was observed that systems possessing low ‘x’ values are highlyselective and active for N-monoalkylation of aniline leading toN-methylaniline. Reaction parameters were properly varied to optimize thereaction conditions for obtaining N-methylaniline selectively and in betteryield. Among the systems CuCr1.75Fe0.25O4 isremarkable due to its very high activity and excellent stability. Under theoptimized conditions N-methylaniline selectivity exceeded 91%. CuCr1.25Fe0.75O4gives better conversion than CuCr1.75Fe0.25O4in CuCr2-xFexO4 series. The Lewis acid sitesof the catalysts are mainly responsible for the good catalytic performance. © 2014 BCREC UNDIP. All rights reservedSubmitted: 18th July 2013; Revised: 5th November 2013; Accepted: 1st December 2013[How to Cite: George, R., George, K., Sugunan, S. (2014. Activity of Aniline Methylation over Fe-Cu-Cr Ternary Spinel Systems. Bulletin of Chemical Reaction Engineering & Catalysis, 9 (1: 39-44. (doi:10.9767/bcrec.9.1.5169.39-44][Permalink/DOI: http://dx.doi.org/10.9767/bcrec.9.1.5169.39-44] 

Tailoring the magnetic properties and magnetorheological behavior of spinel nanocrystalline cobalt ferrite by varying annealing temperature

Czech Academy of Sciences Publication Activity Database

Sedlacik, M.; Pavlinek, V.; Peer, Petra; Filip, Petr

2014-01-01

Roč. 18, č. 43 (2014), s. 6919-6924 ISSN 1477-9226 R&D Projects: GA ČR GA202/09/1626 Grant - others:GA MŠk(CZ) ED2.1.00/03.0111 Institutional support: RVO:67985874 Keywords : spinel nanocrystalline cobalt ferrite * nanoparticles * magnetorheological effect Subject RIV: BK - Fluid Dynamics Impact factor: 4.197, year: 2014

Microscopic origin of the mobility enhancement at a spinel/perovskite oxide heterointerface revealed by photoemission spectroscopy

DEFF Research Database (Denmark)

Schuetz, P.; Christensen, Dennis Valbjørn; Borisov, V.

2017-01-01

The spinel/perovskite heterointerface γ−Al2O3/SrTiO3 hosts a two-dimensional electron system (2DES) with electron mobilities exceeding those in its all-perovskite counterpart LaAlO3/SrTiO3 by more than an order of magnitude, despite the abundance of oxygen vacancies which act as electron donors a...

Oxidation Characteristics and Electrical Properties of Doped Mn-Co Spinel Reaction Layer for Solid Oxide Fuel Cell Metal Interconnects

Directory of Open Access Journals (Sweden)

Pingyi Guo

2018-01-01

Full Text Available To prevent Cr poisoning of the cathode and to retain high conductivity during solid oxide fuel cell (SOFC operation, Cu or La doped Co-Mn coatings on a metallic interconnect is deposited and followed by oxidation at 750 °C. Microstructure and composition of coatings after preparation and oxidation is analyzed by X-ray diffraction (XRD and scanning electron microscopy (SEM. High energy micro arc alloying process, a low cost technique, is used to prepare Cu or La doped Co-Mn coatings with the metallurgical bond. When coatings oxidized at 750 °C in air for 20 h and 100 h, Co3O4 is the main oxide on the surface of Co-38Mn-2La and Co-40Mn coatings, and (Co,Mn3O4 spinel continues to grow with extended oxidation time. The outmost scales of Co-33Mn-17Cu are mainly composed of cubic MnCo2O4 spinel with Mn2O3 after oxidation for 20 h and 100 h. The average thickness of oxide coatings is about 60–70 μm after oxidation for 100 h, except that Co-40Mn oxide coatings are a little thicker. Area-specific resistance of Cu/La doped Co-Mn coatings are lower than that of Co-40Mn coating. (Mn,Co3O4/MnCo2O4 spinel layer is efficient at blocking the outward diffusion of chromium and iron.

Magnetic ordering in the spinel compound Li[Mn2?xLix]O4(x = 0,0.04)

NARCIS (Netherlands)

Gaddy, J.; Lamsal, J.; Petrovic, M.; Montfrooij, W.; Schmets, A.; Vojta, T.

2009-01-01

The two B-site ions Mn3+ and Mn4+ in the stoichiometric spinel structure LiMn2O4 form a complex, columnar ordered pattern below the charge-ordering transition at room temperature. On further cooling to below 66 K, the system develops long-range antiferromagnetic order. In contrast, whereas

Multifunctional thick-film structures based on spinel ceramics for environment sensors

International Nuclear Information System (INIS)

Vakiv, M; Hadzaman, I; Klym, H; Shpotyuk, O; Brunner, M

2011-01-01

Temperature sensitive thick films based on spinel-type NiMn 2 O 4 -CuMn 2 O 4 -MnCo 2 O 4 manganites with p- and p + -types of electrical conductivity and their multilayer p + -p structures were studied. These thick-film elements possess good electrophysical characteristics before and after long-term ageing test at 170 deg. C. It is shown that degradation processes connected with diffusion of metallic Ag into film grain boundaries occur in one-layer p-and p + -conductive films. Some part of the p + -p structures were of high stability, the relative electrical drift being no more than 1 %.

Distribution of solute atoms in β- and spinel Si6-zAlzOzN8-z by Al K-edge x-ray absorption near-edge structure

International Nuclear Information System (INIS)

Tatsumi, Kazuyoshi; Mizoguchi, Teruyasu; Yoshioka, Satoru; Tanaka, Isao; Yamamoto, Tomoyuki; Suga, Takeo; Sekine, Toshimori

2005-01-01

Local environments of solutes in β- and spinel Si 6-z Al z O z N 8-z are investigated by means of Al K x-ray absorption near-edge structure. The experimental spectra are found to be the same throughout the wide solubility range. This suggests that the local environments of Al are independent of the solute concentration. First-principles band-structure calculations are systematically made to interpret the experimental spectra. Effect of a core hole was included into the calculation. Theoretical spectra were obtained using variety of different model structures constructed by a set of plane-wave pseudopotentials calculations in our previous study [K. Tatsumi, I. Tanaka, H. Adachi, and M. Yoshiya, Phys. Rev. B 66, 165210 (2002)]. The numbers of models were 51 and 45 for both β and spinel, respectively. They are classified and averaged according to the local atomic structure of Al solutes. The combination of experimental spectra and theoretical results can unambiguously lead to the conclusion that Al atoms are preferentially coordinated by O atoms in both β and spinel phases. This is consistent with the conclusion obtained by the first-principles total-energy calculations. In the spinel phase, Al atoms are found to be located preferentially at the octahedral cationic site. This agrees with the conclusion in a recent report on the nuclear magnetic resonance experiment

Swelling of spinel after low-dose neutron irradiation

International Nuclear Information System (INIS)

Coghlan, W.A.; Clinard, F.W. Jr.; Itoh, N.; Greenwood, L.R.

1986-01-01

Swelling was determined in samples of single-crystal MgAl 2 O 4 spinel, irradiated to doses as high as 8 x 10 22 n/m 2 (E > 0.1 MeV) at approx. =50 0 C in the Omega West Reactor. Swelling effectively saturated at approx. =2 x 10 22 n/m 2 which corresponds to a damage level of only approx. =2 x 10 -3 dpa. In addition subsequent measurements after irradiation have revealed that the samples continued swelling for several weeks. These results imply that irradiation defects begin to interact by recombination and aggregation at low damage levels in this material at 50 0 C and perhaps continue to cluster at room temperature after irradiation. Rate equations have been employed to determine defect concentrations at saturation. Results to date show that the observed swelling is consistent with the number of surviving defects if swelling per Frenkel defect pair is taken to be one atomic volume

Local probing spinel and perovskite complex magnetic systems

CERN Document Server

De Pinho Oliveira, Goncalo; Lima Lopes, Armandina Maria

Materials with multifunctional physical properties are crucial for the modern society, especially those which display a strong coupling between magnetic, lattice and polar degrees of freedom. This by far unexploited capability promises new paradigm-shift technologies for cooling technologies, magnetic data storage, high-frequency magnetic devices, spintronics, and micro-electromechanical systems. Alongside with the understanding of the properties of these materials, the need to improve them and to make them smaller and more efficient is a current goal. Device miniaturization towards very high-density data storage stands also as a trend in modern science and technology. Here, the integration of several functions into one material system has become highly desirable. Research in this area has already highlighted complex magnetic materials with po- tential for multifunctional applications based on spinel type structures like CdMn2O4 or multiferroic CdCr2S4 or even RCrO3 with orthorhombically distorted perovskite ...

Multiple Nebular Gas Reservoirs Recorded by Oxygen Isotope Variation in a Spinel-Rich CAI in CO3 MIL 090019

Science.gov (United States)

Simon, J. I.; Simon, S. B.; Nguyen, A. N.; Ross, D. K.; Messenger, S.

2017-07-01

We conducted NanoSIMS ion imaging studies of a primitive spinel-rich CAI from the MIL 090019 CO3 chondrite. It records radial O-isotopic heterogeneity among multiple occurrences of the same mineral, reflecting distinct nebular O-isotopic reservoirs.

Nanoparticles of spinel and perovskite ferromagnets and prospects for their application in medicine

Energy Technology Data Exchange (ETDEWEB)

Belous, A. G., E-mail: belous@ionc.kar.net, E-mail: solopan@ukr.net, E-mail: yelenicho@ukr.net; Solopan, S. O., E-mail: belous@ionc.kar.net, E-mail: solopan@ukr.net, E-mail: yelenicho@ukr.net; Yelenich, O. V., E-mail: belous@ionc.kar.net, E-mail: solopan@ukr.net, E-mail: yelenicho@ukr.net [Institute of General and Inorganic Chemistry, prospekt Palladina 32-34, 03142 Kyiv (Ukraine); Tovstolytkin, A. I., E-mail: atov@imag.kiev.ua [Institute of Magnetism, bulvar Vernadskoho 36-b, 03142 Kyiv (Ukraine); Kolodiazhnyi, T. V., E-mail: kolodiazhnyi.taras@nims.go.jp [National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044 (Japan); Osinsky, S. P., E-mail: osion@onconet.kiev.ua, E-mail: bybnovskayal@ukr.net; Bubnovskaya, L. N., E-mail: osion@onconet.kiev.ua, E-mail: bybnovskayal@ukr.net [R.E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology, vul. Vasylkivska 45, 03022 Kyiv (Ukraine)

2014-11-05

In this work, nanoparticles of La{sub 0.75}Sr{sub 0.25}MnO{sub 3} compounds with perovskite structure and AFe{sub 2}O{sub 4} (A = Mn, Fe, Co, Ni, Zn) with spinel structure have been synthesized by precipitation from diethylene glycol and microemulsion using Triton X-100 surfactant. Comparative X-ray diffraction and magnetic studies of the synthesized nanoparticles have been carried out. Magnetic fluids prepared from synthesized nanopowders have been characterized by calorimetric measurements of specific loss power (SLP)

Structural and magnetic properties of Zn.sub.x./sub.Mn.sub.3-x./sub.O.sub.4./sub. spinels

Czech Academy of Sciences Publication Activity Database

Nádherný, L.; Maryško, Miroslav; Sedmidubský, D.; Martin, C.

2016-01-01

Roč. 413, Sep (2016), s. 89-96 ISSN 0304-8853 Institutional support: RVO:68378271 Keywords : Zn-Mn-O spinels * solid-state reaction * ferrimagnetic clusters * ZnO Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 2.630, year: 2016

Compositionally heterogeneous podiform chromitite in the Shetland Ophiolite Complex (Scotland): Implications for chromitite petrogenesis and late-stage alteration in the upper mantle portion of a supra-subduction zone ophiolite

Science.gov (United States)

Derbyshire, E. J.; O'Driscoll, B.; Lenaz, D.; Gertisser, R.; Kronz, A.

2013-03-01

The mantle sequence of the ~ 492 Ma Shetland Ophiolite Complex (SOC; Scotland) contains abundant compositionally heterogeneous podiform chromitite bodies enclosed in elongate dunite lenses in the vicinity of the petrological Moho. Chromitite petrogenesis and late-stage alteration events recorded in these seams are examined here using petrography, mineral chemistry and crystal structural data. The resistant nature of Cr-spinel to serpentinisation and other late-stage alteration means that primary igneous compositions are preserved in unaltered crystal cores. Chromitite mineralogy and texture from five sampled localities at The Viels, Hagdale, Harold's Grave, Nikka Vord and Cliff reveal significant inter-pod chemical heterogeneity. The Cr-spinel mineral chemistry is consistent with supra-subduction zone melt extraction from the SOC peridotites. The occurrence of chromitite seams in the centres of the dunite lenses combined with variable Cr-spinel compositions at different chromitite seam localities supports a model of chromitite formation from spatially (and temporally?) fluctuating amounts of melt-rock interaction through channelised and/or porous melt flow. Pervasive serpentinisation of the SOC has led to the almost complete replacement of the primary (mantle) silicate mineral assemblages with serpentine (lizardite with minor chrysotile and antigorite). Magmatic sulphide (e.g., pentlandite) in dunite and chromitite is locally converted to reduced Ni-sulphide varieties (e.g., heazlewoodite and millerite). A post-serpentinisation (prograde) oxidisation event is recorded in the extensively altered Cliff chromitite seams in the west of the studied area, where chromitite Cr-spinel is extensively altered to ferritchromit. The ferritchromit may comprise > 50% of the volume of the Cliff Cr-spinels and contain appreciable quantities of 1-2 μm inclusions of sperrylite (PtAs2) and Ni-arsenide, signifying the coeval formation of these minerals with ferritchromit at

Spinel ferrite nanocrystals embedded inside ZnO: magnetic, electronic andmagneto-transport properties

Energy Technology Data Exchange (ETDEWEB)

Zhou, Shengqiang; Potzger, K.; Xu, Qingyu; Kuepper, K.; Talut, G.; Marko, D.; Mucklich, A.; Helm, M.; Fassbender, J.; Arenholz, E.; Schmidt, H.

2009-08-21

In this paper we show that spinel ferrite nanocrystals (NiFe{sub 2}O{sub 4}, and CoFe{sub 2}O{sub 4}) can be texturally embedded inside a ZnO matrix by ion implantation and post-annealing. The two kinds of ferrites show different magnetic properties, e.g. coercivity and magnetization. Anomalous Hall effect and positive magnetoresistance have been observed. Our study suggests a ferrimagnet/semiconductor hybrid system for potential applications in magneto-electronics. This hybrid system can be tuned by selecting different transition metal ions (from Mn to Zn) to obtain various magnetic and electronic properties.

Nickel permanganate as a precursor in the synthesis of a NiMn2O4 spinel

International Nuclear Information System (INIS)

Schmidt, Jorge A.; Sagua, Aurora E.; Bazan, Julio C.; Prat, Maria R.; Braganza, Maria E.; Moran, Emilio

2005-01-01

The present study describes the preparation, characterization, and thermal decomposition of the compound Ni(MnO 4 ) 2 .xH 2 O, which was synthesized by a coprecipitation method at a low temperature. The role of this compound as a precursor in the synthesis of a Ni-Mn spinel was determined via X-ray, TG-DTA, electron diffraction, and EDAX measurements

Highly siderophile element geochemistry of peridotites and pyroxenites from Horní Bory, Bohemian Massif: Implications for HSE behaviour in subduction-related upper mantle

Czech Academy of Sciences Publication Activity Database

Ackerman, Lukáš; Pitcher, L.; Strnad, L.; Puchtel, I. S.; Jelínek, E.; Walker, R. J.; Rohovec, Jan

2013-01-01

Roč. 100, č. 1 (2013), s. 158-175 ISSN 0016-7037 R&D Projects: GA AV ČR KJB300130902 Institutional research plan: CEZ:AV0Z30130516 Institutional support: RVO:67985831 Keywords : alloy * high pressure * high temperature * igneous geochemistry * isotopic composition * mass balance * nappe * osmium isotope * peridotite * petrography * platinum group element * precipitation (chemistry) * pyroxenite * siderophile element * subduction * sulfide * upper mantle Subject RIV: DD - Geochemistry Impact factor: 4.250, year: 2013

Mantle wedge infiltrated with saline fluids from dehydration and decarbonation of subducting slab.

Science.gov (United States)

Kawamoto, Tatsuhiko; Yoshikawa, Masako; Kumagai, Yoshitaka; Mirabueno, Ma Hannah T; Okuno, Mitsuru; Kobayashi, Tetsuo

2013-06-11

Slab-derived fluids play an important role in heat and material transfer in subduction zones. Dehydration and decarbonation reactions of minerals in the subducting slab have been investigated using phase equilibria and modeling of fluid flow. Nevertheless, direct observations of the fluid chemistry and pressure-temperature conditions of fluids are few. This report describes CO2-bearing saline fluid inclusions in spinel-harzburgite xenoliths collected from the 1991 Pinatubo pumice deposits. The fluid inclusions are filled with saline solutions with 5.1 ± 1.0% (wt) NaCl-equivalent magnesite crystals, CO2-bearing vapor bubbles, and a talc and/or chrysotile layer on the walls. The xenoliths contain tremolite amphibole, which is stable in temperatures lower than 830 °C at the uppermost mantle. The Pinatubo volcano is located at the volcanic front of the Luzon arc associated with subduction of warm oceanic plate. The present observation suggests hydration of forearc mantle and the uppermost mantle by slab-derived CO2-bearing saline fluids. Dehydration and decarbonation take place, and seawater-like saline fluids migrate from the subducting slab to the mantle wedge. The presence of saline fluids is important because they can dissolve more metals than pure H2O and affect the chemical evolution of the mantle wedge.

Electrochemical evaluation of the a carbon-paste electrode modified with spinel manganese(IV) oxide under flow conditions for amperometric determination of lithium

International Nuclear Information System (INIS)

Raymundo-Pereira, Paulo A.; Martin, Cibely S.; Bergamini, Marcio F.; Bocchi, Nerilso; Teixeira, Marcos F.S.

2011-01-01

The participation of cations in redox reactions of manganese oxides provides an opportunity for development of chemical sensors for non-electroactive ions. This paper describes the amperometric determination of lithium ions using carbon-paste electrode modified with spinel manganese(IV) oxide under flow conditions. Systematic investigations were made to optimize the experimental parameters for lithium sensor by flow injection analysis. The detection was based on the measurement of anodic current generated by oxidation of Mn(III) to Mn(IV) at the surface of the electrode and consequently the lithium ions extraction into the spinel structure. An operating potential of 0.50 V (vs. Ag/AgCl/3 KCl mol/L) was exploited for amperometric monitoring. The amperometric signal was linearly dependent on the lithium ions concentration over the range 4.0 x 10 -5 to 1.0 x 10 -3 mol L -1 . The equilibrium constant of insertion/extraction of the lithium ion in the spinel structure, apparent Gibbs energy of insertion, and surface coverage of the electrode with manganese oxide, were calculated by peak charge (Q) in different concentration under flow conditions. Considering selectivity, the peak charge of the sensor was found to be linearly dependent on the ionic radius of the alkaline and earth-alkaline cations.

Sulfur in serpentinized oceanic peridotites: Serpentinization processes and microbial sulfate reduction

Science.gov (United States)

Alt, J.C.; Shanks, Wayne C.

1998-01-01

The mineralogy, contents, and isotopic compositions of sulfur in oceanic serpentinites reflect variations in temperatures and fluid fluxes. Serpentinization of serpentinization of Iberian Margin peridotites occurred at low temperatures (???20??-200??C) and high water/rock ratios. Complete serpentinization and consumption of ferrous iron allowed evolution to higher fO2. Microbial reduction of seawater sulfate resulted in addition of low-??34S sulfide (-15 to -43???) and formation of higher-sulfur assemblages that include valleriite and pyrite. The high SO4/total S ratio of Hess Deep serpentinites (0.89) results in an increase of total sulfur and high ??34S of total sulfur (mean ??? 8???). In contrast, Iberian Margin serpentinites gained large amounts of 34S-poor sulfide (mean total S = 3800 ppm), and the high sulfide/total S ratio (0.61) results in a net decrease in ??34S of total sulfur (mean ??? -5???). Thus serpentinization is a net sink for seawater sulfur, but the amount fixed and its isotopic composition vary significantly. Serpentinization may result in uptake of 0.4-14 ?? 1012 g S yr-1 from the oceans, comparable to isotopic exchange in mafic rocks of seafloor hydrothermal systems and approaching global fluxes of riverine sulfate input and sedimentary sulfide output.

The variation of cationic microstructure in Mn-doped spinel ferrite during calcination and its effect on formaldehyde catalytic oxidation

Energy Technology Data Exchange (ETDEWEB)

Liang, Xiaoliang [CAS Key Laboratory of Mineralogy and Metallogeny, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Guangdong Provincial Key Laboratory of Mineral Physics and Materials, Guangzhou 510640 (China); Liu, Peng [CAS Key Laboratory of Mineralogy and Metallogeny, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Guangdong Provincial Key Laboratory of Mineral Physics and Materials, Guangzhou 510640 (China); He, Hongping, E-mail: hehp@gig.ac.cn [CAS Key Laboratory of Mineralogy and Metallogeny, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Guangdong Provincial Key Laboratory of Mineral Physics and Materials, Guangzhou 510640 (China); Wei, Gaoling [Guangdong Institute of Eco-Environmental and Soil Sciences, Guangzhou 510650 (China); Chen, Tianhu [School of Resources and Environmental Engineering, Hefei University of Technology, Hefei 230009 (China); Tan, Wei; Tan, Fuding [CAS Key Laboratory of Mineralogy and Metallogeny, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Guangdong Provincial Key Laboratory of Mineral Physics and Materials, Guangzhou 510640 (China); Zhu, Jianxi; Zhu, Runliang [CAS Key Laboratory of Mineralogy and Metallogeny, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Guangdong Provincial Key Laboratory of Mineral Physics and Materials, Guangzhou 510640 (China)

2016-04-05

Highlights: • Calcination causes the activity variation of Mn-doped ferrites for HCHO oxidation. • The variation of catalytic activity of ferrites by calcination is non-linear. • Mn enriches on the calcinated ferrite surface in the valence of +3 and +4. • The reduction temperature of surface Mn{sup 4+} species is well correlated to T50. - Abstract: In this study, a series of Mn substituted spinel ferrites calcinated at different temperatures were used as catalysts for the oxidation of formaldehyde (HCHO). X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy and H{sub 2} temperature-programmed reduction were conducted to characterize the structure and physico-chemical properties of catalysts, which were affected by calcination in the range of 200–600 °C. Results show that all the ferrites were with spinel structure, and those calcinated in the range of 300–600 °C were in the phase of maghemite. The calcination changed the valence and distribution of Mn and Fe on the ferrite surface, and accordingly the reducibility of ferrites. The HCHO catalytic oxidation test showed that with the increase of calcination temperature, the activity was initially improved until 400 °C, but then decreased. The variation of HCHO conversion performance was well positively correlated to the variation of reduction temperature of surface Mn{sup 4+} species. The remarkable effect of calcination on the catalytic activity of Mn-doped spinel ferrites for HCHO oxidation was discussed in view of reaction mechanism and variations in cationic microstructure of Mn-doped ferrites.

The variation of cationic microstructure in Mn-doped spinel ferrite during calcination and its effect on formaldehyde catalytic oxidation

International Nuclear Information System (INIS)

Liang, Xiaoliang; Liu, Peng; He, Hongping; Wei, Gaoling; Chen, Tianhu; Tan, Wei; Tan, Fuding; Zhu, Jianxi; Zhu, Runliang

2016-01-01

Highlights: • Calcination causes the activity variation of Mn-doped ferrites for HCHO oxidation. • The variation of catalytic activity of ferrites by calcination is non-linear. • Mn enriches on the calcinated ferrite surface in the valence of +3 and +4. • The reduction temperature of surface Mn"4"+ species is well correlated to T50. - Abstract: In this study, a series of Mn substituted spinel ferrites calcinated at different temperatures were used as catalysts for the oxidation of formaldehyde (HCHO). X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy and H_2 temperature-programmed reduction were conducted to characterize the structure and physico-chemical properties of catalysts, which were affected by calcination in the range of 200–600 °C. Results show that all the ferrites were with spinel structure, and those calcinated in the range of 300–600 °C were in the phase of maghemite. The calcination changed the valence and distribution of Mn and Fe on the ferrite surface, and accordingly the reducibility of ferrites. The HCHO catalytic oxidation test showed that with the increase of calcination temperature, the activity was initially improved until 400 °C, but then decreased. The variation of HCHO conversion performance was well positively correlated to the variation of reduction temperature of surface Mn"4"+ species. The remarkable effect of calcination on the catalytic activity of Mn-doped spinel ferrites for HCHO oxidation was discussed in view of reaction mechanism and variations in cationic microstructure of Mn-doped ferrites.

Degradation of polychlorinated biphenyls using mesoporous iron-based spinels

Energy Technology Data Exchange (ETDEWEB)

Huang, Linyan; Su, Guijin, E-mail: gjsu@rcees.ac.cn; Zhang, Aiqian; Shi, Yali; Xia, Chaobo; Lu, Huijie; Li, Liewu; Liu, Sha; Zheng, Minghui

2013-10-15

Highlights: • The NiFe{sub 2}O{sub 4} had the highest activity in degradation of CB-209, followed by Fe{sub 3}O{sub 4}. • Hydroxyl species, organic acids, PCBs and chlorobenzenes were identified as products. • Three degradation reactions and one combination reaction competitively occurred. • Hydrodechlorination of CB-209 was more favored over Fe{sub 3}O{sub 4} than NiFe{sub 2}O{sub 4}. • Oxidation reaction of CB-209 was more favored over NiFe{sub 2}O{sub 4} than Fe{sub 3}O{sub 4}. -- Abstract: A series of mesoporous iron-based spinel materials were synthesized to degrade polychlorinated biphenyls (PCBs), with CB-209 being used as a model compound. The materials were characterized by X-ray powder diffraction (XRD), pore structure analysis, and X-ray photoelectron spectroscopy (XPS). A comparison of the dechlorination efficiencies (DEs) of the materials revealed that NiFe{sub 2}O{sub 4} had the highest DE, followed by Fe{sub 3}O{sub 4}. Newly produced polychlorinated biphenyls, chlorinated benzenes, hydroxyl species and organic acids were detected by gas chromatography–mass spectrometry, high performance liquid chromatography–mass spectrometry and ion chromatograph. Identification of the intermediate products indicates that three degradation pathways, hydrodechlorination, the breakage of C-C bridge bond and oxidative reaction, accompanied by one combination reaction, are competitively occurring over the iron-based spinels. The relative amounts of produced three NoCB isomers were illustrated by the C-Cl BDEs of CB-209 at meta-, para- and ortho-positions, and their energy gap between HOMO and LUMO. The consumption of the reactive oxygen species caused by the transformation of Fe{sub 3}O{sub 4} into Fe{sub 2}O{sub 3} in the Fe{sub 3}O{sub 4} reaction system, and the existence of the highly reactive O{sub 2}{sup −}· species in the NiFe{sub 2}O{sub 4} reaction system, could provide a reason why the oxidation reaction was more favored over NiFe{sub 2}O

Multifunctional thick-film structures based on spinel ceramics for environment sensors

Energy Technology Data Exchange (ETDEWEB)

Vakiv, M; Hadzaman, I; Klym, H; Shpotyuk, O [Institute of Materials of SRC ' Carat' , 202 Stryjska str., Lviv, 79031 (Ukraine); Brunner, M, E-mail: shpotyuk@novas.lviv.ua, E-mail: klymha@yahoo.com [Fachhochschule Koeln/University of Applied Sciences, 2 Betzdorfer str., Koeln, 50679 (Germany)

2011-04-01

Temperature sensitive thick films based on spinel-type NiMn{sub 2}O{sub 4}-CuMn{sub 2}O{sub 4}-MnCo{sub 2}O{sub 4} manganites with p- and p{sup +}-types of electrical conductivity and their multilayer p{sup +}-p structures were studied. These thick-film elements possess good electrophysical characteristics before and after long-term ageing test at 170 deg. C. It is shown that degradation processes connected with diffusion of metallic Ag into film grain boundaries occur in one-layer p-and p{sup +}-conductive films. Some part of the p{sup +}-p structures were of high stability, the relative electrical drift being no more than 1 %.

Chemical, structural, and electrochemical characterization of 5 V spinel and complex layered oxide cathodes of lithium ion batteries

Science.gov (United States)

Tiruvannamalai Annamalai, Arun Kumar

2007-12-01

Lithium ion batteries have revolutionized the portable electronics market since their commercialization first by Sony Corporation in 1990. They are also being intensively pursued for electric and hybrid electric vehicle applications. Commercial lithium ion cells are currently made largely with the layered LiCoO 2 cathode. However, only 50% of the theoretical capacity of LiCoO 2 can be utilized in practical cells due to the chemical and structural instabilities at deep charge as well as safety concerns. These drawbacks together with the high cost and toxicity of Co have created enormous interest in alternative cathodes. In this regard, spinel LiMn2O4 has been investigated widely as Mn is inexpensive and environmentally benign. However, LiMn 2O4 exhibits severe capacity fade on cycling, particularly at elevated temperatures. With an aim to overcome the capacity fading problems, several cationic substitutions to give LiMn2-yMyO 4 (M = Cr, Fe, Co, Ni, and Cu) have been pursued in the literature. Among the cation-substituted systems, LiMn1.5Ni0.5O 4 has become attractive as it shows a high capacity of ˜ 130 mAh/g (theoretical capacity: 147 mAh/g) at around 4.7 V. With an aim to improve the electrochemical performance of the 5 V LiMn 1.5Ni0.5O4 spinel oxide, various cation-substituted LiMn1.5-yNi0.5-zMy+zO4 (M = Li, Mg, Fe, Co, and Zn) spinel oxides have been investigated by chemical lithium extraction. The cation-substituted LiMn1.5-yNi0.5-zM y+zO4 spinel oxides exhibit better cyclability and rate capability in the 5 V region compared to the unsubstituted LiMn1.5Ni 0.5O4 cathodes although the degree of manganese dissolution does not vary significantly. The better electrochemical properties of LiMn 1.5-yNi0.5-zMy+zO4 are found to be due to a smaller lattice parameter difference among the three cubic phases formed during the charge-discharge process. In addition, while the spinel Li1-xMn1.58Ni0.42O4 was chemically stable, the spinel Li1-xCo2O4 was found to exhibit both

Characterization and evaluation of employment of nanostructured spinel MA on oxidation resistance of graffiti; Caracterizacao e avaliacao do emprego de espinelio MA nanoestruturado na resistencia a oxidacao de grafites

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Vitor, P.A.M.; Guaglianoni, W.C.; Braganca, S.R.; Bergmann, C.P., E-mail: pedroaugusto89@hotmail.com [Universidade Federal do Rio Grande do Sul (LACER/UFRS), Porto Alegre, RS (Brazil). Laboratorio de Materiais Ceramicos

2016-07-01

This study aimed to investigate the obtaining of nanostructured powders of spinel MA (MgAl2O4) via synthesis of combustion in solution (SCS), and the influence of its incorporation in oxidation resistance in natural graphites. The crystalline phase only was obtained after a heat treatment at 900 ° C of the powder as-synthesized. The powders were characterized by differential thermal analysis (DTA) and thermogravimetric (ATG) and crystallographic analysis by X-ray diffraction (XRD) and Raman spectroscopy. The results, using thermogravimetric dynamic and isothermal analysis showed a relationship between embedded content of spinel (as-synthesized and calcined) and the raising of the temperature to start the oxidation process (onset temperature) of the samples. The rate of oxidation is reduced at temperatures from 700 ° C, retarding the oxidation of graphite with increasing level of spinel, but this effect ceases at temperatures above 1000 ° C. (author)

Molecular dynamics simulations of spinels: LiMn2O4 and Li4Mn5O12 at high temperatures