Sample records for high-mg siliceous mafic

  1. Petrology of the Motaghairat mafic-ultramafic complex, Eastern Desert, Egypt: A high-Mg post-collisional extension-related layered intrusion (United States)

    Abdel Halim, Ali H.; Helmy, Hassan M.; Abd El-Rahman, Yasser M.; Shibata, Tomoyuki; El Mahallawi, Mahmoud M.; Yoshikawa, Masako; Arai, Shoji


    The geodynamic settings of the Precambrian mafic-ultramafic complexes in the Eastern Desert of Egypt have important bearing on understanding the geotectonic evolution of the Arabian Nubian Shield. We present a detailed petrological study on a layered mafic-ultramafic intrusion that is located at the contact between the Precambrian continental crust and the Miocene Red Sea oceanic crust. The Motaghairat layered intrusion consists of basal lherzolite, orthopyroxenite, troctolite, olivine gabbro and anorthosite on the top. Variations in modal mineralogy and mineral chemistry along with the chemical composition of these units suggest their derivation from a common high-Mg tholeiitic parent melt through fractional crystallization processes. The parental magma was derived from a metasomatised mantle source. The primitive mantle-normalized patterns of the calculated melts exhibit enrichment in U relative to Th and Ba relative LREE which indicate that the enriched lithospheric mantle source was metasomatised by fluids derived from a subducted oceanic crust rather than by a sediment melt. Geological and petrological evidences suggest that the layered Motaghairat intrusion was emplaced during post-orogenic extension following subduction break-off and lithospheric delamination after the collision between the amalgamated island arc terranes and the Saharan Metacraton. The heat source required to melt the metasomatised lithospheric mantle was derived from the upwelling of hot asthenosphere after the subduction-break-off.

  2. Chromite-rich mafic silicate chondrules in ordinary chondrites: Formation by impact melting (United States)

    Krot, Alexander N.; Rubin, Alan E.


    Chromium-rich chondrules constitute less than 0.1 percent of all ordinary chondrite (OC) chondrules and comprise three groups: chromian-spinel chondrules, chromian-spinel inclusions, and chromite-rich mafic silicate (CRMS) chondrules. Chromian-spinel chondrules (typically 100-300 microns in apparent diameter) exhibit granular, porphyritic and unusual textures and occur mainly in H chondrites. Their morphologies are distinct from the irregularly shaped chromian-spinel inclusions of similar mineralogy. Chromian-spinel chondrules and inclusions consist of grains of chromian-spinel embedded in plagioclase (Pl) or mesostasis of Pl composition. Many also contain accessory ilmenite (Ilm), high-Ca pyroxene (Px), merrillite (Mer), and rare olivine (Ol); some exhibit concentric mineral and chemical zoning. CRMS chondrules (300-1100 microns in apparent diameter) are generally larger than chromian-spinel chondrules and occur in all metamorphosed OC groups. Most CRMS chondrules are nearly spherical although a few are ellipsoidal with a/b aspect ratios ranging up to 1.7. Textures include cryptocrystalline, granular, radial, barred, and porphyritic varieties; some contain apparently relict grains. The chondrules consist of chromite (Chr), Ol and Pl, along with accessory Mer, troilite (Tr), metallic Fe-Ni (Met), Px and Ilm. The mesostasis in CRMS chondrules is nearly opaque in transmitted light; thus, they can be easily recognized in the optical microscope. Based on the similarity of mineralogy and chemistry between CRMS chondrules of different textures (opaque chromite-rich mesostasis, skeletal morphology of Ol grains, similar bulk compositions) we suggest that these chondrules form a genetically related population.

  3. Occurrence and mineral chemistry of chromite and related silicates from the Hongshishan mafic-ultramafic complex, NW China with petrogenetic implications (United States)

    Ruan, Banxiao; Yu, Yingmin; Lv, Xinbiao; Feng, Jing; Wei, Wei; Wu, Chunming; Wang, Heng


    The Hongshishan mafic-ultramafic complex is located in the western Beishan Terrane, NW China, and hosts an economic Ni-Cu deposit. Chromite as accessory mineral from the complex is divided into three types based on its occurrence and morphology. Quantitative electron probe microanalysis (EPMA) have been conducted on the different types of chromites. Type 1 chromite occurs as inclusions within silicate minerals and has relatively homogeneous composition. Type 2 chromite occurs among serpentine, as interstitial phase. Type 3 chromite is zoned and exhibits a sudden change in compositions from core to rim. Type 1 chromite occurs in olivine gabbro and troctolite showing homogeneous composition. This chromite is more likely primary. Interstitial type 2 and zoned type 3 chromite has compositional variation from core to rim and is more likely modified. Abundant inclusions of orthopyroxene, phlogopite and hornblende occur within type 2 and type 3 chromites. The parental melt of type 1 chromite has an estimated composition of 14.5 wt% MgO, 12.3 wt% Al2O3 and 1.9 wt% TiO2 and is characterized by high temperature, picritic affinity, hydrous nature and high Mg and Ti contents. Compositions of chromite and clinopyroxene are distinct from those of Alaskan-type complexes and imply that the subduction-related environment is not reasonable. Post orogenic extension and the early Permian mantle plume are responsible for the emplacement of mafic-ultramafic complexes in the Beishan Terrane. The cores of zoned chromites are classified as ferrous chromite and the rims as ferrian chromite. The formation of ferrian rim involves reaction of ferrous chromite, forsterite and magnetite to produce ferrian chromite and chlorite, or alternaively, the rim can be simply envisioned as the result of external addition of magnetite in solution to the already formed ferrous chromite.

  4. Late Holocene hydrous mafic magmatism at the Paint Pot Crater and Callahan flows, Medicine Lake Volcano, N. California and the influence of H2O in the generation of silicic magmas (United States)

    Kinzler, R.J.; Donnelly-Nolan, J. M.; Grove, T.L.


    This paper characterizes late Holocene basalts and basaltic andesites at Medicine Lake volcano that contain high pre-eruptive H2O contents inherited from a subduction related hydrous component in the mantle. The basaltic andesite of Paint Pot Crater and the compositionally zoned basaltic to andesitic lavas of the Callahan flow erupted approximately 1000 14C years Before Present (14C years B.P.). Petrologic, geochemical and isotopic evidence indicates that this late Holocene mafic magmatism was characterized by H2O contents of 3 to 6 wt% H2O and elevated abundances of large ion lithophile elements (LILE). These hydrous mafic inputs contrast with the preceding episodes of mafic magmatism (from 10,600 to ~3000 14C years B.P.) that was characterized by the eruption of primitive high alumina olivine tholeiite (HAOT) with low H2O (Paint Pot Crater. The influence of H2O on fractional crystallization of hydrous mafic magma and melting of pre-existing granite crust beneath the volcano combined to produce the rhyolite. Fractionation under hydrous conditions at upper crustal pressures leads to the early crystallization of Fe-Mg silicates and the suppression of plagioclase as an early crystallizing phase. In addition, H2O lowers the saturation temperature of Fe and Mg silicates, and brings the temperature of oxide crystallization closer to the liquidus. These combined effects generate SiO2-enrichment that leads to rhyodacitic differentiated lavas. In contrast, low H2O HAOT magmas at Medicine Lake differentiate to iron-rich basaltic liquids. When these Fe-enriched basalts mix with melted granitic crust, the result is an andesitic magma. Since mid-Holocene time, mafic volcanism has been dominated primarily by hydrous basaltic andesite and andesite at Medicine Lake Volcano. However, during the late Holocene, H2O-poor mafic magmas continued to be erupted along with hydrous mafic magmas, although in significantly smaller volumes.

  5. Petrological constraints on the recycling of mafic crystal mushes, magma ascent and intrusion of braided sills in the Torres del Paine mafic complex (Patagonia) (United States)

    Leuthold, Julien; Müntener, Othmar; Baumgartner, Lukas; Putlitz, Benita


    Cumulate and crystal mush disruption and reactivation are difficult to recognise in coarse grained shallow plutonic rocks. Mafic minerals included in hornblende and zoned plagioclase provide snapshots of early crystallization and cumulate formation, but are difficult to interpret in terms of the dynamics of magma ascent and possible links between silicic and mafic rock emplacement. We will present the field relations, the microtextures and the mineral chemistry of the Miocene mafic sill complex of the Torres del Paine intrusive complex (Patagonia, Chile) and its sub-vertical feeder-zone. The mafic sill complex was built up by a succession of braided sills of shoshonitic and high-K calc-alkaline porphyritic hornblende-gabbro and fine grained monzodioritic sills. The mafic units were over-accreted over 41±11 ka, underplating the overlying granite. Local diapiric structures and felsic magma accumulation between sills indicate limited separation of intercumulus liquid from the mafic sills. Anhedral hornblende cores, with olivine + clinopyroxene ± plagioclase ± apatite inclusions, crystallized at temperatures >900°C and pressures of ~300 to ~500 MPa. The corresponding rims and monzodiorite matrix crystallized at 950°C) from the middle crust reservoir to the emplacement level. We show that hornblende-plagioclase thermobarometry is a useful monitor for the determination of segregation conditions of granitic magmas from gabbroic crystal mushes, and for monitoring the evolution of shallow crustal magmatic crystallization, decompression and cooling.

  6. Disequilibrium growth of olivine in mafic magmas revealed by phosphorus zoning patterns of olivine from mafic-ultramafic intrusions (United States)

    Xing, Chang-Ming; Wang, Christina Yan; Tan, Wei


    Olivine from mafic-ultramafic intrusions rarely displays growth zoning in major and some minor elements, such as Fe, Mg and Ni, due to fast diffusion of these elements at high temperatures. These elements in olivine are thus not useful in deciphering magma chamber processes, such as magma convection, multiple injection and mixing. High-resolution X-ray elemental intensity mapping reveals distinct P zoning patterns of olivine from two mafic-ultramafic intrusions in SW China. Polyhedral olivine grains from lherzolite and dunite of the Abulangdang intrusion show P-rich dendrites similar to those observed in volcanic rocks. Rounded olivine grains from net-textured Fe-Ti oxide ores of the Baima layered intrusion have irregular P-rich patches/bands crosscut and interlocked by P-poor olivine domains. P-rich patches/bands contain 250 to 612 ppm P, much higher than P-poor olivine domains with 123 to 230 ppm P. In electron backscattered diffraction (EBSD) maps, P-rich patches/bands within a single olivine grain have the same crystallographic orientation, indicating that they were remnants of the same crystal. Thus, both P-rich patches/bands and P-poor olivine domains in the same grain show a disequilibrium texture and clearly record two-stage growth. The P-rich patches/bands are likely the remnants of a polyhedral olivine crystal that formed in the first stage, whereas the P-poor olivine domains containing rounded Ti-rich magnetite and Fe-rich melt inclusions may have formed from an Fe-rich ambient melt in the second stage. The complex P zoning of olivine can be attributed to the dissolution of early polyhedral olivine and re-precipitation from the Fe-rich ambient melt. The early polyhedral olivine was in chemical disequilibrium with the ambient melt that may have been developed by silicate liquid immiscibility in a crystal mush. Our study implies that olivine crystals in igneous cumulates with an equilibrium appearance may have experienced disequilibrium growth processes

  7. Activity composition relationships in silicate melts

    Energy Technology Data Exchange (ETDEWEB)

    Glazner, A.F.


    Equipment progress include furnace construction and electron microprobe installation. The following studies are underway: phase equilibria along basalt-rhyolite mixing line (olivine crystallization from natural silicic andensites, distribution of Fe and Mg between olivine and liquid, dist. of Ca and Na between plagioclase and liquid), enthalpy-composition relations in magmas (bulk heat capacity of alkali basalt), density model for magma ascent and contamination, thermobarometry in igneous systems (olivine/plagioclase phenocryst growth in Quat. basalt), high-pressure phase equilibria of alkali basalt, basalt-quartz mixing experiments, phase equilibria of East African basalts, and granitic minerals in mafic magma. (DLC)

  8. Interaction of coeval felsic and mafic magmas from the Kanker ...

    Indian Academy of Sciences (India)

    Blobs of mafic magma form as MMEs in the felsic magma and they scatter throughout the pluton due to convection. At a later stage, if mafic magma enters the system after partial crystallization of felsic phase, mechanical interaction between the magmas leads to the formation of fragmented dyke or syn-plutonic mafic dyke.

  9. Transfer of volatiles and metals from mafic to felsic magmas in composite magma chambers: An experimental study (United States)

    Guo, Haihao; Audétat, Andreas


    In order to determine the behavior of metals and volatiles during intrusion of mafic magma into the base of silicic, upper crustal magma chambers, fluid-rock partition coefficients (Dfluid/rock) of Li, B, Na, S, Cl, K, Mn, Fe, Rb, Sr, Ba, Ce, Cu, Zn, Ag, Cd, Mo, As, Se, Sb, Te, W, Tl, Pb and Bi were determined experimentally at 2 kbar and 850 °C close to the solidus of mafic magma. In a first step, volatile-bearing mafic glasses were prepared by melting a natural basaltic trachyandesite in the presence of volatile-bearing fluids at 1200 °C/10 kbar in piston cylinder presses. The hydrous glasses were then equilibrated in subsequent experiments at 850 °C/2 kbar in cold-seal pressure vessels, which caused 80-90% of the melt to crystallize. After 0.5-2.0 days of equilibration, the exsolved fluid was trapped by means of in-situ fracturing in the form of synthetic fluid inclusions in quartz. Both the mafic rock residue and the fluid inclusions were subsequently analyzed by laser-ablation ICP-MS for major and trace elements. Reverse experiments were conducted by equilibrating metal-bearing aqueous solutions with rock powder and then trapping the fluid. In two additional experiments, information on relative element mobilities were obtained by reacting fluids that exsolved from crystallizing mafic magma with overlying silicic melts. The combined results suggest that under the studied conditions S, Cl, Cu, Se, Br, Cd and Te are most volatile (Dfluid/rock >10), followed by Li, B, Zn, As, Ag, Sb, Cs, W, Tl, Pb and Bi (Dfluid/rock = 1-10). Less volatile are Na, Mg, K, Ca, Mn, Fe, Rb, Sr, Mo and Rb (Dfluid/rock 0.1-1), and the least fluid-mobile elements are Al, Si, Ti, Zr, Ba and Ce (Dfluid/rock apatite.

  10. Mafic dykes at the southwestern margin of Eastern Ghats belt ...

    Indian Academy of Sciences (India)

    the dykes indicate that they preserved time-integrated LREE enrichment. In view of the chemical signatures of OIB source, the mafic dykes could as well be related to continental rifting, around. 1.3 Ga, which may have been initiated by intra-plate volcanism. 1. Introduction. Mafic dyke swarms are common in most Archaean.

  11. ArcGIS studies and field relationships of Paleoproterozoic mafic ...

    Indian Academy of Sciences (India)

    Therefore, relative age relationships of distinct mafic dykes have been established for the study area using cross-cutting field relationships and GIS techniques, which shows slightly different picture than other parts of the Eastern Dharwar Craton. It is suggested that NE–SW trending mafic dykes are youngest in age ...

  12. Mafic and related complexes in Galicia: an excursion guide

    NARCIS (Netherlands)

    Arps, C.E.S.; Calsteren, van P.W.C.; Hilgen, J.D.; Kuijper, R.P.; Tex, den E.


    In Galicia occur several polymetamorphic complexes that contain mafic and ultramafic rocks. Mafic volcanics and gabbros are situated in or near the complexes. An episode of metamorphism and granitization encompassed the generation of the volcanics and gabbros. Gravity surveys revealed the existence

  13. Silicate volcanism on Io (United States)

    Carr, M. H.


    This paper is mainly concerned with the nature of volcanic eruptions on Io, taking into account questions regarding the presence of silicates or sulfur as principal component. Attention is given to the generation of silicate magma, the viscous dissipation in the melt zone, thermal anomalies at eruption sites, and Ionian volcanism. According to the information available about Io, it appears that its volcanism and hence its surface materials are dominantly silicic. Several percent of volatile materials such as sulfur, but also including sodium- and potassium-rich materials, may also be present. The volatile materials at the surface are continually vaporized and melted as a result of the high rates of silicate volcanism.

  14. A primitive mantle source for the Neoarchean mafic rocks from the Tanzania Craton

    Directory of Open Access Journals (Sweden)

    Y.A. Cook


    Full Text Available Mafic rocks comprising tholeiitic pillow basalt, dolerite and minor gabbro form the basal stratigraphic unit in the ca. 2.8 to 2.6 Ga Geita Greenstone Belt situated in the NW Tanzania Craton. They outcrop mainly along the southern margin of the belt, and are at least 50 million years older than the supracrustal assemblages against which they have been juxtaposed. Geochemical analyses indicate that parts of the assemblage approach high Mg-tholeiite (more than 8 wt.% MgO. This suite of samples has a restricted compositional range suggesting derivation from a chemically homogenous reservoir. Trace element modeling suggests that the mafic rocks were derived by partial melting within the spinel peridotite field from a source rock with a primitive mantle composition. That is, trace elements maintain primitive mantle ratios (Zr/Hf = 32–35, Ti/Zr = 107–147, producing flat REE and HFSE profiles [(La/Ybpm = 0.9–1.3], with abundances of 3–10 times primitive mantle and with minor negative anomalies of Nb [(Nb/Lapm = 0.6–0.8] and Th [(Th/Lapm = 0.6–0.9]. Initial isotope compositions (ɛNd range from 1.6 to 2.9 at 2.8 Ga and plot below the depleted mantle line suggesting derivation from a more enriched source compared to present day MORB mantle. The trace element composition and Nd isotopic ratios are similar to the mafic rocks outcropping ∼50 km south. The mafic rocks outcropping in the Geita area were erupted through oceanic crust over a short time period, between ∼2830 and ∼2820 Ma; are compositionally homogenous, contain little to no associated terrigenous sediments, and their trace element composition and short emplacement time resemble oceanic plateau basalts. They have been interpreted to be derived from a plume head with a primitive mantle composition.

  15. Nanostructured silicate polymer concrete

    Directory of Open Access Journals (Sweden)

    Figovskiy Oleg L'vovich


    Full Text Available It has been known that acid-resistant concretes on the liquid glass basis have high porosity (up to 18~20 %, low strength and insufficient water resistance. Significant increasing of silicate matrix strength and density was carried out by incorporation of special liquid organic alkali-soluble silicate additives, which block superficial pores and reduce concrete shrinkage deformation. It was demonstrated that introduction of tetrafurfuryloxisilane additive sharply increases strength, durability and shock resistance of silicate polymer concrete in aggressive media. The experiments showed, that the strength and density of silicate polymer concrete increase in case of decreasing liquid glass content. The authors obtained optimal content of silicate polymer concrete, which possesses increased strength, durability, density and crack-resistance. Diffusive permeability of concrete and its chemical resistance has been investigated in various corroding media.

  16. Activity composition relationships in silicate melts. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Glazner, A.F.


    Equipment progress include furnace construction and electron microprobe installation. The following studies are underway: phase equilibria along basalt-rhyolite mixing line (olivine crystallization from natural silicic andensites, distribution of Fe and Mg between olivine and liquid, dist. of Ca and Na between plagioclase and liquid), enthalpy-composition relations in magmas (bulk heat capacity of alkali basalt), density model for magma ascent and contamination, thermobarometry in igneous systems (olivine/plagioclase phenocryst growth in Quat. basalt), high-pressure phase equilibria of alkali basalt, basalt-quartz mixing experiments, phase equilibria of East African basalts, and granitic minerals in mafic magma. (DLC)

  17. Polymer-Layer Silicate Nanocomposites

    DEFF Research Database (Denmark)

    Potarniche, Catalina-Gabriela

    Nowadays, some of the material challenges arise from a performance point of view as well as from recycling and biodegradability. Concerning these aspects, the development of polymer layered silicate nanocomposites can provide possible solutions. This study investigates how to obtain polymer layered...... silicate nanocomposites and their structure-properties relationship. In the first part of the thesis, thermoplastic layered silicates were obtained by extrusion. Different modification methods were tested to observe the intercalation treatment effect on the silicate-modifier interactions. The silicate...

  18. Pseudotachylitic breccia in mafic and felsic rocks (United States)

    Kovaleva, Elizaveta; Huber, Matthew S.


    Impact-produced pseudotachylitic breccia (PTB) is abundant in the core of the Vredefort impact structure and was found in many pre-impact lithologies (e.g., Reimold and Colliston, 1994; Gibson et al., 1997). The mechanisms involved in the process of forming this rock remain highly debated, and various authors have discussed many possible models. We investigate PTB from two different rock types: meta-granite and meta-gabbro and test how lithology controls the development of PTB. We also report on clast transport between different lithologies. In the core of the Vredefort impact structure, meta-granite and meta-gabbro are observed in contact with each other, with an extensive set of PTB veins cutting through both lithologies. Microstructural analyses of the PTB veins in thin sections reveals differences between PTBs in meta-granite and meta-gabbro. In granitic samples, PTB often develops along contacts of material with different physical properties, such as a contact with a migmatite or pegmatite vein. Nucleation sites of PTB have features consistent with ductile deformation and shearing, such as sigmoudal-shaped clasts and dragged edges of the veins. Preferential melting of mafic and hydrous minerals takes place (e.g., Reimold and Colliston, 1994; Gibson et al., 2002). Refractory phases remain in the melt as clasts and form reaction rims. In contrast, PTB in meta-gabbro develop in zones with brittle deformation, and do not exploit existing physical contacts. Cataclastic zones develop along the faults and progressively produce ultracataclasites and melt. Thus, PTB veins in meta-gabbro contain fewer clasts. Clasts usually represent multi-phase fragments of host rock and not specific phases. Such fragments often originate from the material trapped between two parallel or horse-tail faults. The lithological control on the development of PTB does not imply that PTB develops independently in different lithologies. We have observed granitic clasts within PTB veins in meta

  19. Cambrian intermediate-mafic magmatism along the Laurentian margin: Evidence for flood basalt volcanism from well cuttings in the Southern Oklahoma Aulacogen (U.S.A.) (United States)

    Brueseke, Matthew E.; Hobbs, Jasper M.; Bulen, Casey L.; Mertzman, Stanley A.; Puckett, Robert E.; Walker, J. Douglas; Feldman, Josh


    The Southern Oklahoma Aulocogen (SOA) stretches from southern Oklahoma through the Texas panhandle and into Colorado and New Mexico, and contains mafic through silicic magmatism related to the opening of the Iapetus Ocean during the early Cambrian. Cambrian magmatic products are best exposed in the Wichita Mountains (Oklahoma), where they have been extensively studied. However, their ultimate derivation is still somewhat contentious and centers on two very different models: SOA magmatism has been suggested to occur via [1] continental rifting (with or without mantle plume emplacement) or [2] transform-fault related magmatism (e.g., leaky strike-slip faults). Within the SOA, the subsurface in and adjacent to the Arbuckle Mountains in southern Oklahoma contains thick sequences of mafic to intermediate lavas, intrusive bodies, and phreatomagmatic deposits interlayered with thick, extensive rhyolite lavas, thin localized tuffs, and lesser silicic intrusive bodies. These materials were first described in the Arbuckle Mountains region by a 1982 drill test (Hamilton Brothers Turner Falls well) and the best available age constraints from SOA Arbuckle Mountains eruptive products are 535 to 540 Ma. Well cuttings of the mafic through intermediate units were collected from that well and six others and samples from all but the Turner Falls and Morton wells are the focus of this study. Samples analyzed from the wells are dominantly subalkaline, tholeiitic, and range from basalt to andesite. Their overall bulk major and trace element chemistry, normative mineralogy, and Srsbnd Nd isotope ratios are similar to magmas erupted/emplaced in flood basalt provinces. When compared with intrusive mafic rocks that crop out in the Wichita Mountains, the SOA well cuttings are geochemically most similar to the Roosevelt Gabbros. New geochemical and isotope data presented in this study, when coupled with recent geophysical work in the SOA and the coeval relationship with rhyolites, indicates

  20. Geochemistry and geochronology of the mafic dikes in the Taipusi ...

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Earth System Science; Volume 126; Issue 5. Geochemistry and ... In this contribution, we present first-hand whole-rock major and trace elements, zircon U–Pb geochronology and in situ trace element geochemistry data for these mafic rocks, which reveal their petrogenesis and tectonic evolution.

  1. Mafic rocks from Erinpura gneiss terrane in the Sirohi region ...

    Indian Academy of Sciences (India)

    metric wings indicating synkinematic recrystallisation of hornblende clasts during shearing. .... of mica laths around stretched clasts (Siegesmund et al 1995). In the mafic rocks, the magnetic lin- eation is in the direction ..... notable differences in the enrichment levels, shape and pattern underline distinct source characteris-.

  2. Interaction of coeval felsic and mafic magmas from the Kanker ...

    Indian Academy of Sciences (India)

    R Elangovan


    Oct 5, 2017 ... Connemara, Ireland; Mineral. Petrol. 76(1) 63–74. Blundy J D and Sparks R S J 1992 Petrogenesis of mafic inclusions in granitoids of the Adamello Massif, Italy;. J. Petrol. 33(5) 1039–1104. Chatterjee A 1970 Structure, tectonics and metamorphism in a part of south Bastar, MP; Quat. J. Geol. Min. Met. Soc.

  3. Geochemistry and Petrogenesis of Biabanak–Bafq Mafic Mgmatism ...

    Indian Academy of Sciences (India)


    Cretaceous impact of the Trindad mantle plume: Evidence from large–volume, mafic, potassic magmatism in SE Brazil. J. Petrol. 36(1), 189–229. Ghorbani M 2013 ... Haghipour A 1974 Etude géologique de la region de BiabanakBafq (Iran Central); petrologie et tectonique du precambrien et de sa couverture, Ph.D. thesis,.

  4. Petrological and geochemical studies of ultramafic–mafic rocks from ...

    Indian Academy of Sciences (India)

    The shearing produced S-C fabric, ultra-mylonite in the high grade metamorphic country rocks. Three episodes of metamorphism have been recorded in the rocks of CGC ..... No filter is used for major oxides. Vacuum path is 20/40 kV. Standard used for calibration is BHVO-1. Trace element abundances (table 6) of mafic and.

  5. ArcGIS studies and field relationships of Paleoproterozoic mafic ...

    Indian Academy of Sciences (India)

    Google Earth Image and cross-cutting field relationships of distinct Paleoproterozoic mafic dykes from south of Devarakonda area in the Eastern Dharwar Craton has been studied to establish relative emplace- ment ages. The Devarakonda, covering an area of ∼700 km2, shows spectacular cross-cutting field rela- tionships ...

  6. Geochemical constraints on the evolution of mafic and felsic rocks in ...

    Indian Academy of Sciences (India)

    The presence of pillow basalt marks the eruption of these rocks in a subaqueous environment. Intermittent eruption of mafic and felsic magmas resulted in the formation of rhyolite, mafic pyroclasts, and tuff. Mixing and mingling of the felsic and mafic magmas resulted in the hybrid rock andesite. Granites are emplaced later, ...

  7. Silicates in Alien Asteroids (United States)


    This plot of data from NASA's Spitzer Space Telescopes shows that asteroid dust around a dead 'white dwarf' star contains silicates a common mineral on Earth. The data were taken primarily by Spitzer's infrared spectrograph, an instrument that breaks light apart into its basic constituents. The yellow dots show averaged data from the spectrograph, while the orange triangles show older data from Spitzer's infrared array camera. The white dwarf is called GD 40.

  8. Spectroscopic analysis (FTIR, Raman) of water in mafic and intermediate glasses and glass inclusions

    Energy Technology Data Exchange (ETDEWEB)

    Mercier, Maxime [Laboratoire Pierre Sue, CNRS-CEA, CE-Saclay, 91191 Gif sur Yvette (France); Departement des Sciences de la Terre, Interactions et Dynamique des Environnements de Surface, Universite Paris-Sud 11, 91405 Orsay Cedex (France); Di Muro, Andrea [Laboratoire de Geologie des Systemes Volcaniques, IPGP, UMR 7154, 4 Place Jussieu, 75005 Paris (France); Metrich, Nicole; Belhadj, Olfa [Laboratoire Pierre Sue, CNRS-CEA, CE-Saclay, 91191 Gif sur Yvette (France); Giordano, Daniele [Institut de Ciencies de la Terra Jaume Almera CSIC, c/Luis Sole Sabaris s/n, 08028 Barcelona (Spain); Mandeville, Charles W. [American Museum of Natural History, Central Park West at 79th Street, New York, NY 10024-5192 (US)


    Micro-Raman spectroscopy, even though a very promising technique, is not still routinely applied to analyse H{sub 2}O in silicate glasses. The accuracy of Raman water determinations critically depends on the capability to predict and take into account both the matrix effects (bulk glass composition) and the analytical conditions on band intensities. On the other hand, micro-Fourier transform infrared spectroscopy is commonly used to measure the hydrous absorbing species (e.g., hydroxyl OH and molecular H{sub 2}O) in natural glasses, but requires critical assumptions for the study of crystal-hosted glasses. Here, we quantify for the first time the matrix effect of Raman external calibration procedures for the quantification of the total H{sub 2}O content (H{sub 2}O(T) = OH{sup -} + H{sub 2}O{sub m}) in natural silicate glasses. The procedures are based on the calibration of either the absolute (external calibration) or scaled (parameterization) intensity of the 3550 cm{sup -1} band. A total of 67 mafic (basanite, basalt) and intermediate (andesite) glasses hosted in olivines, having between 0.2 and 4.8 wt% of H{sub 2}O, was analysed. Our new dataset demonstrates, for given water content, the height (intensity) of Raman H{sub 2}OT band depends on glass density, reflectance and water environment. Hence this matrix effect must be considered in the quantification of H{sub 2}O by Raman spectroscopy irrespective of the procedure, whereas the parameterization mainly helps to predict and verify the self-consistency of the Raman results. In addition, to validate the capability of the micro-Raman to accurately determine the H{sub 2}O content of multicomponent aluminosilicate glasses, a subset of 23 glasses was analysed by both micro-Raman and micro-FTIR spectroscopy using the band at 3550 cm{sup -1}. We provide new FTIR absorptivity coefficients {epsilon}{sub 3550}) for basalt (62.80 {+-} 0.8 L mol{sup -1} cm{sup -1}) and basanite (43.96 {+-} 0.6 L mol{sup -1} cm{sup -1

  9. Thermochemistry of Silicates (United States)

    Costa, Gustavo; Jacobson, Nathan


    The thermodynamic properties of vapor and condensed phases of silicates are crucial in many fields of science. These quantities address fundamental questions on the formation, stability, transformation, and physical properties of silicate minerals and silicate coating compositions. Here the thermodynamic activities of silica and other species in solid solution have been measured by the analysis of the corresponding high temperature vapors using Knudsen Effusion Mass Spectrometry (KEMS). In first set of experiments KEMS has been used to examine the volatility sequence of species (Fe, SiO, Mg, O2 and O) present in the vapor phase during heating of fosterite-rich olivine (Fo93Fa7) up to 2400 C and to measure the Fe, SiO and Mg activities in its solid solution. The data of fosterite-rich olivine are essential for thermochemical equilibrium models to predict the atmospheric and surface composition of hot, rocky exoplanets (Lava Planets). In the second set of experiments the measured thermodynamic activities of the silica in Y2O3-SiO2 and Yb2O3-SiO2 systems are used to assess their reactivity and degradation recession as environmental barrier coatings (EBCs) in combustion environments (e.g. non-moveable parts of gas turbine engine).

  10. Silicic magma entering a basaltic magma chamber: eruptive dynamics and magma mixing — an example from Salina (Aeolian islands, Southern Tyrrhenian Sea) (United States)

    Calanchi, Natale; de Rosa, Rosanna; Mazzuoli, Roberto; Rossi, Pierluigi; Santacroce, Roberto; Ventura, Guido


    The Pollara tuff-ring resulted from two explosive eruptions whose deposits are separated by a paleosol 13 Ka old. The oldest deposits (LPP, about 0.2 km3) consist of three main fall units (A, B, C) deposited from a subplinian column whose height (7 14 km) increased with time from A to C, as a consequence of the increased magma discharge rate during the eruption (1 8x106 kg/s). A highly variable juvenile population characterizes the eruption. Black, dense, highly porphyritic, mafic ejecta (SiO2=50 55%) almost exclusively form A deposits, whereas grey, mildly vesiculated, mildly porphyritic pumice (SiO2=56 67%) and white, highly vesiculated, nearly aphyric pumice (SiO2=66 71%) predominate in B and C respectively. Mafic cumulates are abundant in A, while crystalline lithic ejecta first appear in B and increase upward. The LPP result from the emptying of an unusual and unstable, compositionally zoned, shallow magma chamber in which high density mafic melts capped low density salic ones. Evidence of the existence of a short crystal fractionation series is found in the mafic rocks; the andesitic pumice results from complete blending between rhyolitic and variously fractionated mafic melts (salic component up to 60 wt%), whereas bulk dacitic compositions mainly result from the presence of mafic xenocrysts within rhyolitic glasses. Viscosity and composition-mixing diagrams show that blended liquids formed when the visosities of the two end members had close values. The following model is suggested: 1. A rhyolitic magma rising through the metamorphic basement enterrd a mafic magma chamber whose souter portions were occupied by a highly viscous, mafic crystal mush. 2. Under the pressure of the rhyolitic body the nearly rigid mush was pushed upwards and mafic melts were squeezed against the walls of the chamber, beginning roof fracturing and mingling with silicic melts. 3. When the equilibrium temperature was reached between mafic and silicic melts, blended liquids rapidly

  11. Hybridization in the subvolcanic Jaala-Iitti complex and its petrogenetic relation to rapakivi granites and associated mafic rocks of southeastern Finland

    Directory of Open Access Journals (Sweden)

    Salonsaari, P.T.


    of rapid crystallization. The mass-fraction of mafic magma (Xm in the hybrid rock is up to 0.3. The Xm in hybrid MMEs and pillow-like MMEs varies from 0.4 to 0.9. The temperature difference between the two magmas probably caused convection that spread the disaggregated mafic magma throughout the postulated layered magma chamber. The injected mafic magma simultaneously mingled and mixed with the felsic magma which was superheated, assisting the chemical exchange. The interaction of hybrid MME magma with the hybrid magmas was possibly made more effective by diffusion of fluorine from the felsic magma into the mafic magma. The composition of minerals indicates intensive interaction of the mafic magma and the felsic host, with the temperature of equilibrium being in the range of 900° to 750°C. The crystallization of granites of the complex occurred between 850-650°C, with an oxygen fugacity parallel or slightly below the QFM buffer. Besides geochemical evidence, a hybrid origin for the rocks is also shown by the composition of Fe-Mg silicates. Pyroxenes, however, from the hybrid rocks and MMEs show disequilibrium having crystallized at various stages of the hybridization event. Mantling of the alkali feldspar megacrysts by micrographic plagioclase- quartz intergrowth and plagioclase shells has taken place at a temperature of 850° to 750°C at a pressure under 2 kbar. In the main part of the Wiborg batholith, any indication of large-scale hybridization between rapakivi and diabase magmas are lacking. A possible high velocity underplate beneath the batholith may have been a heat source for the partially crystallized rapakivi granite magma to produce corroded partially melted alkali feldspar megacrysts and the rapakivi texture without intensive magma mixing.

  12. Contribution from Mafic Melt to the Zhireken Porphyry Mo-Cu Deposit, Eastern Transbaikalia, Russia: Evidence from Mafic Microgranular Enclaves

    Directory of Open Access Journals (Sweden)



    Full Text Available Mafic microgranular enclaves (MME were formed in felsic ore-bearing porphyries from the Zhireken por-phyry Mo-Cu deposit, eastern Transbaikalia, Russia. Porphyry rocks were emplaced during the Upper Jurassic. Most of the enclaves are globular, oval-shaped and intermediate in composition (54% SiO2. The MME from the Zhireken deposit often contain the same minerals as the host granite porphyries, though their chemical compositions are different. Accessory magnetite in MME shows higher Cr2O3 and Cu contents while, apatite reveals higher Cl and S concentrations compared to those in host porphyries. Mafic melt may have made substantial contribution for the overall budget of sulphur and ore metals in evolving felsic magma and hydrothermal fluid of the Zhireken deposit. Higher contents of Pd (684 ppb and Pt (299 ppb in molybdenites of the Zhireken deposit, as well as high temperatures (1020-910°C of formation of porphyry rock melt inclusions, indirectly suggest a contribution from mafic melt derived from the mantle.

  13. Marquette Island: A Distinct Mafic Lithology Discovered by Opportunity (United States)

    Mittlefehldt, David W.; Gellert, R.; Herkenhoff, K. E.; Clark, B. C.; Cohen, B. A.; Fleischer, I.; Jolliff, B. L.; Klingelhoefer, G.; Ming, D. W.; Yingst, R. A.


    While rolling over the Meridiani Planum sedimentary terrane, the rover Opportunity has occasionally discovered large, > 10 cm erratics. Most of these have proven to be meteorites [1], but one - Bounce Rock - is a martian basaltic rock similar in composition to the meteorite EETA79001 lithology B [2]. Presently, Opportunity is intensively investigating an --30 cm tall rock named Marquette Island that may be a distinct type of martian mafic lithology. We report the results of its continuing investigation using the Microscopic Imager (MI); Mossbauer Spectrometer (MB) and Alpha Particle X-ray Spectrometer (APXS). A companion abstract discusses the results of Panoramic Camera (Pancam) imaging of the rock [3].

  14. Catchment-wide weathering and erosion rates of mafic, ultramafic, and granitic rock from cosmogenic meteoric 10Be/9Be ratios (United States)

    Dannhaus, N.; Wittmann, H.; Krám, P.; Christl, M.; von Blanckenburg, F.


    Quantifying rates of weathering and erosion of mafic rocks is essential for estimating changes to the oceans alkalinity budget that plays a significant role in regulating atmospheric CO2 levels. In this study, we present catchment-wide rates of weathering, erosion, and denudation measured with cosmogenic nuclides in mafic and ultramafic rock. We use the ratio of the meteoric cosmogenic nuclide 10Be, deposited from the atmosphere onto the weathering zone, to stable 9Be, a trace metal released by silicate weathering. We tested this approach in stream sediment and water from three upland forested catchments in the north-west Czech Republic. The catchments are underlain by felsic (granite), mafic (amphibolite) and ultramafic (serpentinite) lithologies. Due to acid rain deposition in the 20th century, the waters in the granite catchment exhibit acidic pH, whereas waters in the mafic catchments exhibit neutral to alkaline pH values due to their acid buffering capability. The atmospheric depositional 10Be flux is estimated to be balanced with the streams' dissolved and particulate meteoric 10Be export flux to within a factor of two. We suggest a correlation method to derive bedrock Be concentrations, required as an input parameter, which are highly heterogeneous in these small catchments. Derived Earth surface metrics comprise (1) Denudation rates calculated from the 10Be/9Be ratio of the "reactive" Be (meaning sorbed to mineral surfaces) range between 110 and 185 t km-2 y-1 (40 and 70 mm ky-1). These rates are similar to denudation rates we obtained from in situ-cosmogenic 10Be in quartz minerals present in the bedrock or in quartz veins in the felsic and the mafic catchment. (2) The degree of weathering, calculated from the fraction of 9Be released from primary minerals as a new proxy, is about 40-50% in the mafic catchments, and 10% in the granitic catchment. Lastly, (3) erosion rates were calculated from 10Be concentrations in river sediment and corrected for sorting

  15. Petrology, geochemistry and tectonic settings of the mafic dikes and ...

    Indian Academy of Sciences (India)

    R. Narasimhan (Krishtel eMaging) 1461 1996 Oct 15 13:05:22

    Petrological and geochronological studies of several cross cutting dikes show that these dikes may be related to lineament reactivation during the evolution of the Cuddapah basin. The Cuddapah basin area is interesting from a global tectonic perspective since, tholeiitic and high-Mg dikes similar in age and composition to.

  16. The timing of compositionally-zoned magma reservoirs and mafic 'priming' weeks before the 1912 Novarupta-Katmai rhyolite eruption (United States)

    Singer, Brad S.; Costa, Fidel; Herrin, Jason S.; Hildreth, Wes; Fierstein, Judy


    The June, 6, 1912 eruption of more than 13 km3 of dense rock equivalent (DRE) magma at Novarupta vent, Alaska was the largest of the 20th century. It ejected >7 km3 of rhyolite, ∼1.3 km3 of andesite and ∼4.6 km3 of dacite. Early ideas about the origin of pyroclastic flows and magmatic differentiation (e.g., compositional zonation of reservoirs) were shaped by this eruption. Despite being well studied, the timing of events that led to the chemically and mineralogically zoned magma reservoir remain poorly known. Here we provide new insights using the textures and chemical compositions of plagioclase and orthopyroxene crystals and by reevaluating previous U-Th isotope data. Compositional zoning of the magma reservoir likely developed a few thousand years before the eruption by several additions of mafic magma below an extant silicic reservoir. Melt compositions calculated from Sr contents in plagioclase fill the compositional gap between 68 and 76% SiO2 in whole pumice clasts, consistent with uninterrupted crystal growth from a continuum of liquids. Thus, our findings support a general model in which large volumes of crystal-poor rhyolite are related to intermediate magmas through gradual separation of melt from crystal-rich mush. The rhyolite is incubated by, but not mixed with, episodic recharge pulses of mafic magma that interact thermochemically with the mush and intermediate magmas. Hot, Mg-, Ca-, and Al-rich mafic magma intruded into, and mixed with, deeper parts of the reservoir (andesite and dacite) multiple times. Modeling the relaxation of the Fe-Mg concentrations in orthopyroxene and Mg in plagioclase rims indicates that the final recharge event occurred just weeks prior to the eruption. Rapid addition of mass, volatiles, and heat from the recharge magma, perhaps aided by partial melting of cumulate mush below the andesite and dacite, pressurized the reservoir and likely propelled a ∼10 km lateral dike that allowed the overlying rhyolite to reach the

  17. Environmental silicate nano-biocomposites

    CERN Document Server

    Pollet, Eric


    Environmental Silicate Nano-Biocomposites focuses on nano-biocomposites, which are obtained by the association of silicates such as bioclays with biopolymers. By highlighting recent developments and findings, green and biodegradable nano-composites from both renewable and biodegradable polymers are explored. This includes coverage of potential markets such as packaging, agricultures, leisure and the fast food industry. The knowledge and experience of more than twenty international experts in diverse fields, from chemical and biochemical engineering to applications, is brought together in four different sections covering: Biodegradable polymers and Silicates, Clay/Polyesters Nano-biocomposites, Clay/Agropolymers Nano-biocomposites, and Applications and biodegradation of Nano-biocomposites. By exploring the relationships between the biopolymer structures, the processes, and the final properties Environmental Silicate Nano-Biocomposites explains how to design nano-materials to develop new, valuable, environmenta...

  18. Interpreting the I-Xe system in individual silicate grains from Toluca IAB (United States)

    Pravdivtseva, O. V.; Meshik, A. P.; Hohenberg, C. M.; Petaev, M.


    Detailed isotopic and mineralogical studies of silicate inclusions separated from a troilite nodule of the Toluca IAB iron meteorite reveal the presence of radiogenic 129Xe in chlorapatite, plagioclase, perryite, and pyroxene grains. Subsequent I-Xe studies of 32 neutron-irradiated pyroxene grains indicate that high-Mg and low-Mg pyroxenes have distinctive I-Xe signatures. The I-Xe system in high-Mg pyroxenes closed at 4560.5 ± 2.4 Ma, probably reflecting exsolution of silicates from the melt, while the low-Mg pyroxenes closed at 4552.0 ± 3.7 Ma, 8.5 Ma later, providing a means for determining the cooling rate at the time of exsolution. If the host Toluca graphite-troiliterich inclusion formed after the breakup and reassembly of the IAB parent body as has been suggested, the I-Xe ages of the high-Mg pyroxenes separated from this inclusions indicate that this catastrophic impact occurred not later than 4560.5 Ma, 6.7 Ma after formation of CAIs. The cooling rate at the time of silicates exsolution in Toluca is 14.5 ± 10.0 °C/Ma.

  19. An essential factor for high Mg2+ tolerance of Staphylococcus aureus

    Directory of Open Access Journals (Sweden)

    Joshua Armitano


    Full Text Available Internal bacterial concentration of Mg2+, the most abundant divalent cation in living cells, is estimated to be in the single millimolar range. However, many bacteria will thrive in media with only micromolars of Mg2+, by using a range of intensely studied and highly efficient import mechanisms, as well as in media with very high magnesium concentration, presumably mediated by currently unknown export mechanisms. Staphylococcus aureus has a particularly high Mg2+ tolerance for a pathogen, growing unimpaired in up to 770 mM Mg2+, and we here identify SA0657, a key factor in this tolerance. The predicted domain structure of SA0657 is shared with a large number of proteins in bacteria, archaea and even eukarya, for example CorB from Salmonella and the human CNNM protein family. One of the shared domains, a CBS pair potentially involved in Mg2+ sensing, contains the conserved Glycine326 which we establish to be a key residue for SA0657 function. In light of our findings, we propose the name MpfA, Magnesium Protection Factor A, for SA0657.

  20. Preliminary study of the characteristics of a high Mg containing Al-Mg-Si alloy (United States)

    Yan, F.; McKay, B. J.; Fan, Z.; Chen, M. F.


    An Al-20Mg-4Si high Mg containing alloy has been produced and its characteristics investigated. The as-cast alloy revealed primary Mg2Si particles evenly distributed throughout an α-Al matrix with a β-Al3Mg2 fully divorced eutectic phase observed in interdendritic regions. The Mg2Si particles displayed octahedral, truncated octahedral, and hopper morphologies. Additions of Sb, Ti and Zr had a refining influence reducing the size of the Mg2Si from 52 ± 4 μm to 25 ± 0.1 μm, 35 ± 1 μm and 34 ± 1 μm respectively. HPDC tensile test samples could be produced with a 0.6 wt.% Mn addition which prevented die soldering. Solution heating for 1 hr was found to dissolve the majority of the Al3Mg2 eutectic phase with no evidence of any effect on the primary Mg2Si. Preliminary results indicate that the heat treatment has a beneficial effect on the elongation and the UTS.

  1. Using mineral geochemistry to decipher slab, mantle, and crustal input in the generation of high-Mg andesites and basaltic andesites from the northern Cascade Arc (United States)

    Sas, May; DeBari, Susan; Clynne, Michael A.; Rusk, Brian G.


    To better understand the role of slab melt in the petrogenesis of North Cascades magmas, this study focuses on petrogenesis of high-Mg lavas from the two northernmost active volcanoes in Washington. High-Mg andesites (HMA) and basaltic andesites (HMBA) in the Cascade Arc have high Mg# [molar Mg/(Mg+Fe2+)] relative to their SiO2 contents, elevated Nd/Yb, and are Ni- and Cr-enriched. The rock units examined here include the Tarn Plateau HMBA (51.8–54.0 wt% SiO2, Mg# 68–70) and Glacier Creek HMA (58.3–58.7 wt% SiO2, Mg# 63–64) from the Mount Baker Volcanic Field, and the Lightning Creek HMBA (54.8–54.6 SiO2, Mg# 69–73) from Glacier Peak. This study combines major and trace element compositions of minerals and whole rocks to test several petrogenetic hypotheses and to determine which, if any, are applicable to North Cascades HMA and HMBA. In the Tarn Plateau HMBA, rare earth element (REE) equilibrium liquids calculated from clinopyroxene compositions have high Nd/Yb that positively correlates with Mg#. This correlation suggests an origin similar to that proposed for Aleutian adakites, where intermediate, high Nd/Yb slab-derived melts interact with the overlying mantle to become Mg-rich, and subsequently mix with low Nd/Yb, mantle-derived mafic magmas with lower Mg#. In the Glacier Creek HMA, elevated whole-rock MgO and SiO2 contents resulted from accumulation of xenocrystic olivine and differentiation processes, respectively, but the cause of high Nd/Yb is less clear. However, high whole-rock Sr/P (fluid mobile/fluid immobile) values indicate a mantle source that was fluxed by an enriched, hydrous slab component, likely producing the observed high Nd/Yb REE signature. The Lightning Creek HMBA is a hybridized rock unit with at least three identifiable magmatic components, but only one of which has HMA characteristics. Cr and Mg contents in Cr-spinel and olivine pairs in this HMA component suggest that its source is a strongly depleted mantle, and high

  2. Understanding silicate hydration from quantitative analyses of hydrating tricalcium silicates (United States)

    Pustovgar, Elizaveta; Sangodkar, Rahul P.; Andreev, Andrey S.; Palacios, Marta; Chmelka, Bradley F.; Flatt, Robert J.; d'Espinose de Lacaillerie, Jean-Baptiste


    Silicate hydration is prevalent in natural and technological processes, such as, mineral weathering, glass alteration, zeolite syntheses and cement hydration. Tricalcium silicate (Ca3SiO5), the main constituent of Portland cement, is amongst the most reactive silicates in water. Despite its widespread industrial use, the reaction of Ca3SiO5 with water to form calcium-silicate-hydrates (C-S-H) still hosts many open questions. Here, we show that solid-state nuclear magnetic resonance measurements of 29Si-enriched triclinic Ca3SiO5 enable the quantitative monitoring of the hydration process in terms of transient local molecular composition, extent of silicate hydration and polymerization. This provides insights on the relative influence of surface hydroxylation and hydrate precipitation on the hydration rate. When the rate drops, the amount of hydroxylated Ca3SiO5 decreases, thus demonstrating the partial passivation of the surface during the deceleration stage. Moreover, the relative quantities of monomers, dimers, pentamers and octamers in the C-S-H structure are measured. PMID:27009966

  3. Oxygen isotope composition of mafic magmas at Vesuvius (United States)

    Dallai, L.; Cioni, R.; Boschi, C.; D'Oriano, C.


    The oxygen isotope composition of olivine and clinopyroxene from four plinian (AD 79 Pompeii, 3960 BP Avellino), subplinian (AD 472 Pollena) and violent strombolian (Middle Age activity) eruptions were measured to constrain the nature and evolution of the primary magmas of the last 4000 years of Mt. Vesuvius activity. A large set of mm-sized crystals was accurately separated from selected juvenile material of the four eruptions. Crystals were analyzed for their major and trace element compositions (EPMA, Laser Ablation ICP-MS), and for 18O/16O ratios. As oxygen isotope composition of uncontaminated mantle rocks on world-wide scale is well constrained (δ18Oolivine = 5.2 ± 0.3; δ18Ocpx = 5.6 ± 0.3 ‰), the measured values can be conveniently used to monitor the effects of assimilation/contamination of crustal rocks in the evolution of the primary magmas. Instead, typically uncontaminated mantle values are hardly recovered in Italian Quaternary magmas, mostly due to the widespread occurrence of crustal contamination of the primary magmas during their ascent to the surface (e.g. Alban Hills, Ernici Mts., and Aeolian Islands). Low δ18O values have been measured in olivine from Pompeii eruption (δ18Oolivine = 5.54 ± 0.03‰), whereas higher O-compositions are recorded in mafic minerals from pumices or scoria of the other three eruptions. Measured olivine and clinopyroxene share quite homogeneous chemical compositions (Olivine Fo 85-90 ; Diopside En 45-48, respectively), and represent phases crystallized in near primary mafic magmas, as also constrained by their trace element compositions. Data on melt inclusions hosted in crystals of these compositions have been largely collected in the past demonstrating that they crystallized from mafic melt, basaltic to tephritic in composition. Published data on volatile content of these melt inclusions reveal the coexistence of dissolved water and carbon dioxide, and a minimum trapping pressure around 200-300 MPa, suggesting

  4. Oxygen isotope geochemistry of mafic magmas at Mt. Vesuvius (United States)

    Dallai, Luigi; Raffaello, Cioni; Chiara, Boschi; Claudia, D'oriano


    Pumice and scoria from different eruptive layers of Mt. Vesuvius volcanic products contain mafic minerals consisting of High-Fo olivine and Diopsidic Pyroxene. These phases were crystallized in unerupted trachibasaltic to tephritic magmas, and were brought to surface by large phonolitic/tephri-phonolitic (e.g. Avellino and Pompei) and/or of tephritic and phono-tephritic (Pollena) eruptions. A large set of these mm-sized crystals was accurately separated from selected juvenile material and measured for their chemical compositions (EPMA, Laser Ablation ICP-MS) and 18O/16O ratios (conventional laser fluorination) to constrain the nature and evolution of the primary magmas at Mt. Vesuvius. Uncontaminated mantle δ18O values are hardly recovered in Italian Quaternary magmas, mostly due to the widespread occurrence of crustal contamination of the primary melts during their ascent to the surface (e.g. Alban Hills, Ernici Mts., and Aeolian Islands). At Mt. Vesuvius, measured olivine and clinopyroxene share quite homogeneous chemical compositions (Olivine Fo 85-90 ; Diopside En 45-48, respectively), and represent phases crystallized in near primary mafic magmas. Trace element composition constrains the near primary nature of the phases. Published data on volatile content of melt inclusions hosted in these crystals reveal the coexistence of dissolved water and carbon dioxide, and a minimum trapping pressure around 200-300 MPa, suggesting that crystal growth occurred in a reservoir at about 8-10 km depth. Recently, experimental data have suggested massive carbonate assimilation (up to about 20%) to derive potassic alkali magmas from trachybasaltic melts. Accordingly, the δ18O variability and the trace element content of the studied minerals suggest possible contamination of primary melts by an O-isotope enriched, REE-poor contaminant like the limestone of Vesuvius basement. Low, nearly primitive δ18O values are observed for olivine from Pompeii eruption, although still

  5. Final report on the safety assessment of aluminum silicate, calcium silicate, magnesium aluminum silicate, magnesium silicate, magnesium trisilicate, sodium magnesium silicate, zirconium silicate, attapulgite, bentonite, Fuller's earth, hectorite, kaolin, lithium magnesium silicate, lithium magnesium sodium silicate, montmorillonite, pyrophyllite, and zeolite. (United States)

    Elmore, Amy R


    This report reviews the safety of Aluminum, Calcium, Lithium Magnesium, Lithium Magnesium Sodium, Magnesium Aluminum, Magnesium, Sodium Magnesium, and Zirconium Silicates, Magnesium Trisilicate, Attapulgite, Bentonite, Fuller's Earth, Hectorite, Kaolin, Montmorillonite, Pyrophyllite, and Zeolite as used in cosmetic formulations. The common aspect of all these claylike ingredients is that they contain silicon, oxygen, and one or more metals. Many silicates occur naturally and are mined; yet others are produced synthetically. Typical cosmetic uses of silicates include abrasive, opacifying agent, viscosity-increasing agent, anticaking agent, emulsion stabilizer, binder, and suspending agent. Clay silicates (silicates containing water in their structure) primarily function as adsorbents, opacifiers, and viscosity-increasing agents. Pyrophyllite is also used as a colorant. The International Agency for Research on Cancer has ruled Attapulgite fibers >5 microm as possibly carcinogenic to humans, but fibers Cosmetic Ingredient Review (CIR. The Cosmetic Ingredient Review (CIR) Expert Panel concluded that the extensive pulmonary damage in humans was the result of direct occupational inhalation of the dusts and noted that lesions seen in animals were affected by particle size, fiber length, and concentration. The Panel considers that most of the formulations are not respirable and of the preparations that are respirable, the concentration of the ingredient is very low. Even so, the Panel considered that any spray containing these solids should be formulated to minimize their inhalation. With this admonition to the cosmetics industry, the CIR Expert Panel concluded that these ingredients are safe as currently used in cosmetic formulations. The Panel did note that the cosmetic ingredient, Talc, is a hydrated magnesium silicate. Because it has a unique crystalline structure that differs from ingredients addressed in this safety assessment, Talc is not included in this report.

  6. Identification and quantification of gabbro cumulate partial melting in mafic igneous complexes (United States)

    Leuthold, J.


    In mafic magma chambers, olivine, plagioclase and clinopyroxene fractionate along the basaltic liquid line of descent. Ol-rich, troctolite and gabbro cumulates crystallize. Hot primitive magma sills are regularly injected into igneous complexes where they heat and partially melt surrounding hot rocks, percolate, hybridize and crystallize new and secondary phases (see Figure [1]). Here, I quantify the effect of gabbro cumulate partial melting and hybridization with invading primitive basalt using field observations, Cpx microtexture and core-rim geochemical profiles from the Rum sill complex (Scotland). I have run gabbro-basalt hybrid equilibrium and kinetic experiments to test the effect of gabbro assimilation on the basalt liquid and solid lines of descent. Rum poikilitic gabbro resorbed Cpx cores are overgrown by Cr-, Al-, Zr- and REE-depleted interstitial rim with high Mg#, Eu* and Sr* (see [2]). Plg is reversely zoned. Fractional crystallization fails to explain the combined dissolution texture and incoherent compatible and incompatible elements zoning. Gabbro cumulate partial melting produces a Cpx-depleted residue and a melt that is saturated in Cpx, depleted in Cr, Al, Zr and REE and with high SiO2 and Mg# contents [1]. REE-poor Cpx rim crystallized from a hybrid basalt-gabbro magma, despite a lower DREE. In picrite-gabbro kinetic experiments reacted at conditions where Ol, Plg and Cpx are stable in gabbro but only Ol is stable in primitive basalt (1210°C, NNO-2), gabbro Ol and Cpx are anhedral and reversely zoned and Plg is euhedral. In the reaction rim, Cpx is absent, Ol anhedral grains are small and Cr-Spl abundance strongly increased (to 1.8 vol%). Troctolite small-scale partial melting and hybridization with primitive basalt produces a hybrid Al-rich melt that is Spl over-saturated. Gabbro partial melting products can be very difficult to distinguish from cumulates crystallized along the basalt liquid line of descent, because of the limited

  7. Silicic magmas from the Emeishan large igneous province, Southwest China: Petrogenesis and their link with the end-Guadalupian biological crisis (United States)

    Xu, Yi-Gang; Chung, Sun-Lin; Shao, Hui; He, Bin


    The Emeishan large igneous province in SW China comprises a bimodal mafic-silicic suite with the silicic rocks occurring at the uppermost part of the thick lava sequence. The silicic rocks have an age of 257-263 Ma, and are thus roughly coeval with the Guadalupian-Loping (G-L) boundary event. Most silicic rocks (trachyte and rhyolite) from the Emeishan province have rather uniform ɛNd values (+ 1 to + 2.9) that are comparable with the uncontaminated high-Ti basalts. This fact and the remarkably narrow ranges of incompatible element ratios (e.g., Zr/Nb) of the basalt-silicic suite indicate a genetic relationship between basalt and silicic members. The significant difference between the Emeishan rocks and the experimental melts of hydrated basaltic crust, suggests the fractional crystallization of basaltic magma, rather than crustal melting, as the major petrogenetic process for the formation of silicic rocks. Indeed, their major and trace element trends can be modeled by fractionation of the observed mineral phases (feldspar, clinopyroxene, Fe-Ti oxide and apatite). In contrast to the virtually closed system differentiation processes associated with trachytes, the rhyolites may have experienced interaction with upper crustal material during ascent. The geochemical characteristics and recent assessment of timing of the Emeishan volcanism suggest the Emeishan rhyolites as the potential source of the widespread clay bed at the G-L boundary in south China. This enhanced the causal link between the Emeishan eruption and the end-Guadalupian biological crisis.


    Directory of Open Access Journals (Sweden)

    V. N. Yaglov


    Full Text Available The paper proposes a technology for obtaining bricks on the basis of lime-silica mixtures where chemical interactions are practically completely realized in dispersive state at the stage of preparation of binding contact maturing and raw mixture as a whole. The role of forming operation (moulding is changed in principle because in this case conversion of dispersive system into a rock-like solid occurs and due to this the solid obtains complete water-resistance in contact with water immediately after forming operation. Theoretical basis for the developed technology is capability of silicate dispersive substances (hydrated calcium silicate to transit in non-stable state, to form a rock-like water-resistant solid in the moment of mechanical load application during forming process. Specific feature of the proposed method is an exclusion of additional operations for autoclaving of products from the process of obtaining a silicate brick.Synthetic hydrated calcium silicate in contrast to natural ones are more uniform in composition and structure, they contain less impurities and they are characterized by dispersive composition and due to the mentioned advantages they find wider practical application. Contact-condensation binders permit to manipulate product properties on their basis and ensure maximum correspondence to the requirements of the concrete application. Raw material sources for obtaining synthetic hydrated calcium silicates are practically un-limited because calcium-silicon containing substances are found as in various technogenic wastes so in natural compounds as well. So the problem for obtaining hydrated calcium silicates having contact-condensation ability for structure formation becomes more and more actual one. This transition is considered as dependent principally on arrangement rate of substance particles which determined the level of its instability.

  9. Battery components employing a silicate binder (United States)

    Delnick, Frank M [Albuquerque, NM; Reinhardt, Frederick W [Albuquerque, NM; Odinek, Judy G [Rio Rancho, NM


    A battery component structure employing inorganic-silicate binders. In some embodiments, casting or coating of components may be performed using aqueous slurries of silicates and electrode materials or separator materials.

  10. Submarine silicic volcanism: Processes and products

    Digital Repository Service at National Institute of Oceanography (India)

    Kalangutkar, N.G.; Iyer, S.D.

    The occurrence of submarine silicic volcanics is rare at the mid-oceanic ridges, abyssal depths, seamounts and fracture zones. Hydrothermal processes are active in submarine silicic environments and are associated with host ores of Cu, Au, Ag, Pb...

  11. Amended Silicated for Mercury Control

    Energy Technology Data Exchange (ETDEWEB)

    James Butz; Thomas Broderick; Craig Turchi


    Amended Silicates{trademark}, a powdered, noncarbon mercury-control sorbent, was tested at Duke Energy's Miami Fort Station, Unit 6 during the first quarter of 2006. Unit 6 is a 175-MW boiler with a cold-side electrostatic precipitator (ESP). The plant burns run-of-the-river eastern bituminous coal with typical ash contents ranging from 8-15% and sulfur contents from 1.6-2.6% on an as-received basis. The performance of the Amended Silicates sorbent was compared with that for powdered activated carbon (PAC). The trial began with a period of baseline monitoring during which no sorbent was injected. Sampling during this and subsequent periods indicated mercury capture by the native fly ash was less than 10%. After the baseline period, Amended Silicates sorbent was injected at several different ratios, followed by a 30-day trial at a fixed injection ratio of 5-6 lb/MMACF. After this period, PAC was injected to provide a comparison. Approximately 40% mercury control was achieved for both the Amended Silicates sorbent and PAC at injection ratios of 5-6 lbs/MMACF. Higher injection ratios did not achieve significantly increased removal. Similar removal efficiencies have been reported for PAC injection trials at other plants with cold-side ESPs, most notably for plants using medium to high sulfur coal. Sorbent injection did not detrimentally impact plant operations and testing confirmed that the use of Amended Silicates sorbent does not degrade fly ash quality (unlike PAC). The cost for mercury control using either PAC or Amended Silicates sorbent was estimated to be equivalent if fly ash sales are not a consideration. However, if the plant did sell fly ash, the effective cost for mercury control could more than double if those sales were no longer possible, due to lost by-product sales and additional cost for waste disposal. Accordingly, the use of Amended Silicates sorbent could reduce the overall cost of mercury control by 50% or more versus PAC for locations where

  12. Late Neoproterozoic layered mafic intrusion of arc-affinity in the Arabian-Nubian Shield: A case study from the Shahira layered mafic intrusion, southern Sinai, Egypt

    Energy Technology Data Exchange (ETDEWEB)

    Azer, M.K.; Obeid, M.A.; Gahalan, H.A.


    The Shahira Layered Mafic Intrusion (SLMI), which belongs to the late Neoproterozoic plutonic rocks of the Arabian-Nubian Shield, is the largest layered mafic intrusion in southern Sinai. Field relations indicate that it is younger than the surrounding metamorphic rocks and older than the post-orogenic granites. Based on variation in mineral paragenesis and chemical composition, the SLMI is distinguished into pyroxene-hornblende gabbro, hornblende gabbro and diorite lithologies. The outer zone of the mafic intrusion is characterized by fine-grained rocks (chilled margin gabbroic facies), with typical subophitic and/or microgranular textures. Different rock units from the mafic intrusion show gradational boundaries in between. They show some indications of low grade metamorphism, where primary minerals are transformed into secondary ones. Geochemically, the Shahira layered mafic intrusion is characterized by enrichment in LILE relative to HFSE (e.g. Nb, P, Zr, Ti, Y), and LREE relative to HREE [(La/Lu)n= 4.75–8.58], with subalkaline characters. It has geochemical characteristics of pre-collisional arc-type environment. The geochemical signature of the investigated gabbros indicates partial melting of mantle wedge in a volcanic-arc setting, being followed by fractional crystallization and crustal contamination. Fractional crystallization processes played a vital role during emplacement of the Shahira intrusion and evolution of its mafic and intermediate rock units. The initial magma was evolved through crystallization of hornblende which was caused by slight increasing of H2O in the magma after crystallization of liquidus olivine, pyroxene and Ca-rich plagioclase. The gabbroic rocks crystallized at pressures between 4.5 and 6.9kbar (~15–20km depth). Whereas, the diorites yielded the lowest crystallization pressure between 1.0 to 4.4Kbar (<10km depth). Temperature was estimated by several geothermometers, which yielded crystallization temperatures ranging from 835

  13. Proterozoic Geomagnetic Field Geometry from Mafic Dyke Swarms (United States)

    Panzik, J. E.; Evans, D. A.


    Pre-Mesozoic continental reconstructions and paleoclimatic inferences from paleomagnetism rely critically upon the assumption of a time-averaged geocentric axial dipole (GAD) magnetic field. We have been testing the GAD assumption empirically, by compiling paleomagnetic remanence directional variations among coeval volcanic rock suites distributed over large areas of the Earth's surface. We compute virtual geomagnetic poles (VGPs) from site-mean remanence data using either a pure GAD model, or alternative models with varying amounts of zonal quadrupole or octupole fields. Rastering through quadrupole vs. octupole space, we produce contour plots of precision/dispersion for the mean of VGPs in each computation. Using the 0-5 Ma volcanics global database as a test, our method shows results consistent with the compilations of Schneider & Kent (1990, Rev. Geophys. 28, 71-96) and McElhinny et al. (1996, JGR 101, 25007-25027), notably reproducing the reversal asymmetry in a significant (order 3%) quadrupolar contribution. Performing the same test on ancient mafic dyke swarms, the Karoo-Ferrar large igneous province (ca. 0.18 Ga) and the central Atlantic magmatic province (CAMP) (0.20 Ga) datasets are consistent with a range of models, including both GAD and independent estimates of non-GAD contributions derived from global tectonic reconstructions (Torsvik & Van der Voo, 2002, GJI 151, 771-794). The method is limited by paleolongitudinal restriction of ancient LIPs, for similarly restrictive sub-sampling of the 0-5 Ma volcanic data can generate results that differ dramatically from the global mean (e.g., the far-sided offset of VGPs relative to the spin axis). Analysis of pre-Pangean datasets is limited by the uncertainty of tectonic reconstructions, but within solely the intact North American (Laurentian) craton, the Franklin (ca. 0.72), Mackenzie (ca. 1.27) and Matachewan (2.45 Ga) dyke swarms are used as Pre-Mesozoic targets that have large areal coverage. None of the

  14. Petrological and geochemical studies of ultramafic-mafic rocks from the North Puruliya Shear Zone (eastern India) (United States)

    Mandal, Aditi; Ray, Arijit


    Ultramafic and mafic rocks occur within a linear belt, trending nearly E-W along North Puruliya Shear Zone of the Chhotanagpur Gneissic Complex (CGC). These rocks are classified as gabbro, norite, gabbro-norite, dolerite, diorite, olivine-websterite and lherzolite. Mafic rocks (Group 1) often occur in association with ultramafic variants (Group 2) and sometimes in isolation. A genetic link has been established between these mafic and ultramafic rocks using disposition of ultramafic and mafic rocks in the outcrop, systematic variation in modal mineralogy, co-linearity of plots in biaxial chemical variation diagram. Chemical composition of biotite and clinopyroxene reveal calc-alkaline nature and arc signature in these mafic-ultramafic rocks and whole rock geochemical characters indicate similarity with arc magma in subduction zone setting. The high values of Mg no. (47-81) and Al 2 O 3 (5.5-17.9) of mafic rocks indicate primitive, aluminous nature of the parental melt and presence of amphibole and biotite indicate its hydrous nature. The parent mafic melt evolved through fractionation of olivine, spinel, clinopyroxene and plagioclase. The crystal cumulates gave rise to the ultramafic rocks and the associated mafic rocks formed from residual melt. Crustal contamination played an important role in magmatic evolution as evident from variation in abundance of Rb in different lithomembers. Mafic-ultramafic rocks of the present study have been compared with intra-cratonic layered complexes, mafic-ultramafic rocks of high grade terrain, Alaskan type ultramafic-mafic complex and ophiolites. It is observed that the ultramafic-mafic rocks of present study have similarity with Alaskan type complex.

  15. Emergence of silicic continents as the lower crust peels off on a hot plate-tectonic Earth (United States)

    Chowdhury, Priyadarshi; Gerya, Taras; Chakraborty, Sumit


    The rock record and geochemical evidence indicate that continental recycling has been occurring since the early history of the Earth. The stabilization of felsic continents in place of Earth's early mafic crust about 3.0 to 2.0 billion years ago, perhaps due to the initiation of plate tectonics, implies widespread destruction of mafic crust during this time interval. However, the physical mechanisms of such intense recycling on a hotter, (late) Archaean and presumably plate-tectonic Earth remain largely unknown. Here we use thermomechanical modelling to show that extensive recycling via lower crustal peeling-off (delamination but not eclogitic dripping) during continent-continent convergence was near ubiquitous during the late Archaean to early Proterozoic. We propose that such destruction of the early mafic crust, together with felsic magmatism, may have caused both the emergence of silicic continents and their subsequent isostatic rise, possibly above the sea level. Such changes in the continental character have been proposed to influence the Great Oxidation Event and, therefore, peeling-off plate tectonics could be the geodynamic trigger for this event. A transition to the slab break-off controlled syn-orogenic recycling occurred as the Earth aged and cooled, leading to reduced recycling and enhanced preservation of the continental crust of present-day composition.

  16. Late Cretaceous intraplate silicic volcanic rocks from the Lake Chad region: An extension of the Cameroon volcanic line? (United States)

    Shellnutt, J. G.; Lee, T.-Y.; Torng, P.-K.; Yang, C.-C.; Lee, Y.-H.


    Silicic volcanic rocks at Hadjer el Khamis, near Lake Chad, are considered to be an extension of the Cameroon volcanic line (CVL) but their petrogenetic association is uncertain. The silicic rocks are divided into peraluminous and peralkaline groups with both rock types chemically similar to within-plate granitoids. In situ U/Pb zircon dating yielded a mean 206Pb/238U age of 74.4 ± 1.3 Ma indicating the magmas erupted ˜10 million years before the next oldest CVL rocks (i.e., ˜66 Ma). The Sr isotopes (i.e., ISr = 0.7021-0.7037) show a relatively wide range but the Nd isotopes (i.e., 143Nd/144Ndi = 0.51268-0.51271) are uniform and indicate that the rocks were derived from a moderately depleted mantle source. Thermodynamic modeling shows that the silicic rocks likely formed by fractional crystallization of a mafic parental magma but that the peraluminous rocks were affected by low temperature alteration processes. The silicic rocks are more isotopically similar to Late Cretaceous basalts identified within the Late Cretaceous basins (i.e., 143Nd/144Ndi = 0.51245-0.51285) of Chad than the uncontaminated CVL rocks (i.e., 143Nd/144Ndi = 0.51270-0.51300). The age and isotopic compositions suggest the silicic volcanic rocks of the Lake Chad region are related to Late Cretaceous extensional volcanism in the Termit basin. It is unlikely that the silicic volcanic rocks are petrogenetically related to the CVL but it is possible that magmatism was structurally controlled by suture zones that formed during the opening of the Central Atlantic Ocean and/or the Pan-African Orogeny.

  17. Tailoring polymer properties with layered silicates (United States)

    Xu, Liang

    Polymer layered silicate nanocomposites have found widespread applications in areas such as plastics, oil and gas production, biomedical, automotive and information storage, but their successful commercialization critically depends on consistent control over issues such as complete dispersion of layered silicate into the host polymer and optimal interaction between the layered silicates and the polymers. Polypropylene is a commercially important polymer but usually forms intercalated structures with organically modified layered silicate upon mixing, even it is pre-treated with compatibilizing agent such as maleic anhydride. In this work, layered silicate is well dispersed in ammonium modified polypropylene but does not provide sufficient reinforcement to the host polymer due to poor interactions. On the other hand, interactions between maleic anhydride modified polypropylene and layered silicate are fine tuned by using a small amount of maleic anhydride and mechanical strength of the resultant nanocomposites are significantly enhanced. In particular, the melt rheological properties of layered silicate nanocomposites with maleic anhydride functionalized polypropylene are contrasted to those based on ammonium-terminated polypropylene. While the maleic anhydride treated polypropylene based nanocomposites exhibit solid-like linear dynamic behavior, consistent with the formation of a long-lived percolated nanoparticle network, the single-end ammonium functionalized polypropylene based nanocomposites demonstrated liquid-like behavior at comparable montmorillonite concentrations. The differences in the linear viscoelasticity are attributed to the presence of bridging interaction in maleic anhydride functionalized nanocomposites, which facilitates formation of a long-lived silicate network mediated by physisorbed polymer chains. Further, the transient shear stress of the maleic anhydride functionalized nanocomposites in start-up of steady shear is a function of the shear

  18. Nanoscale zinc silicate from phytoliths (United States)

    Qadri, S. B.; Gorzkowski, E. P.; Rath, B. B.; Feng, C. R.; Amarasinghe, R.; Freitas, J. A.; Culbertson, J. C.; Wollmershauser, J. A.


    We report a faster, less expensive method of producing zinc silicate nanoparticles. Such particles are used in high volume to make phosphors and anti-corrosion coatings. The approach makes use of phytoliths (plant rocks), which are microscopic, amorphous, and largely silicate particles embedded in plants, that lend themselves to being easily broken down into nanoparticles. Nanoparticles of Zn2SiO4 were produced in a two stage process. In the refinement stage, plant residue, mixed with an appropriate amount of ZnO, was heated in an argon atmosphere to a temperature exceeding 1400 °C for four to six hours and then heated in air at 650 °C to remove excess carbon. TEM shows 50-100 nm nanoparticles. Raman scattering indicates that only the -Zn2SiO4 crystalline phase was present. X-ray analysis indicated pure rhombohedral R 3 bar phase results from using rice/wheat husks. Both samples luminesced predominantly at 523 nm when illuminated with X-rays or UV laser light.

  19. Interaction of coeval felsic and mafic magmas from the Kanker granite, Pithora region, Bastar Craton, Central India (United States)

    Elangovan, R.; Krishna, Kumar; Vishwakarma, Neeraj; Hari, K. R.; Ram Mohan, M.


    Field and petrographic studies are carried out to characterize the interactions of mafic and felsic magmas from Pithora region of the northeastern part of the Bastar Craton. The MMEs, syn-plutonic mafic dykes, cuspate contacts, magmatic flow textures, mingling and hybridization suggest the coeval emplacement of end member magmas. Petrographic evidences such as disequilibrium assemblages, resorption textures, quartz ocelli, rapakivi and poikilitic textures suggest magma mingling and mixing phenomena. Such features of mingling and mixing of the felsic and mafic magma manifest the magma chamber processes. Introduction of mafic magmas into the felsic magmas before initiation of crystallization of the latter, results in hybrid magmas under the influence of thermal and chemical exchange. The mechanical exchange occurs between the coexisting magmas due to viscosity contrast, if the mafic magma enters slightly later into the magma chamber, then the felsic magma starts to crystallize. Blobs of mafic magma form as MMEs in the felsic magma and they scatter throughout the pluton due to convection. At a later stage, if mafic magma enters the system after partial crystallization of felsic phase, mechanical interaction between the magmas leads to the formation of fragmented dyke or syn-plutonic mafic dyke. All these features are well-documented in the study area. Field and petrographic evidences suggest that the textural variations from Pithora region of Bastar Craton are the outcome of magma mingling, mixing and hybridization processes.

  20. Silica-poor, mafic alkaline lavas from ocean islands and continents ...

    Indian Academy of Sciences (India)

    R. Narasimhan (Krishtel eMaging) 1461 1996 Oct 15 13:05:22

    Strongly silica-poor (ne-normative), mafic alkaline lavas generally represented by olivine nephelin- ites, nephelinites, melilitites, and olivine melilitites have erupted at various locations during Earth's history. On the basis of bulk-rock Mg#, high concentrations of Na2O, TiO2, and K2O, and trace element geochemistry, it has ...

  1. Geochemistry of PGE in mafic rocks of east Khasi Hills, Shillong ...

    Indian Academy of Sciences (India)

    1Department of Geology, University of Calcutta, 35 Ballygunge Circular Road, Kolkata 700 019, India. .... geological succession it is apparent that the mafic ..... dyk e. Plagio clase. (fresh and saussiritized),. O livine. 5. 3. 9 .05. 49.02. 1.54. L. T quartz, m uscovite, a mphib o le, n ormativ e epidote, biotite. HT: H igh. T. iO. 2.

  2. Thermal and Transport Properties of Mafic and Ultramafic Rocks of Oman Ophiolite

    Directory of Open Access Journals (Sweden)

    Sayyadul Arafin


    Full Text Available Thermal and other physical properties of rocks and minerals are of considerable significance for deriving mineralogical and compositional models of the Earth's mantle. We have determined these properties for the mafic rock such as gabbro and ultramafic rock like harzburgite of the Oman ophiolite suite by utilizing the Debye characteristic property ,Θ-

  3. Silicates materials of high vacuum technology

    CERN Document Server

    Espe, Werner


    Materials of High Vacuum Technology, Volume 2: Silicates covers silicate insulators of special importance to vacuum technology. The book discusses the manufacture, composition, and physical and chemical properties of technical glasses, quartz glass, quartzware, vycor glass, ceramic materials, mica, and asbestos.

  4. Zircon U-Pb ages and Hf isotopic compositions of alkaline silicic magmatic rocks in the Phan Si Pan-Tu Le region, northern Vietnam: Identification of a displaced western extension of the Emeishan Large Igneous Province (United States)

    Usuki, Tadashi; Lan, Ching-Ying; Tran, Trong Hoa; Pham, Thi Dung; Wang, Kuo-Lung; Shellnutt, Gregory J.; Chung, Sun-Lin


    In-situ zircon U-Pb and Hf isotope analyses were carried out for alkaline silicic magmatic rocks from the Phan Si Pan-Tu Le region in northern Vietnam to constrain their possible sources and to determine their petrogenetic relationship with the Emeishan Large Igneous Province (ELIP), SW China. Nine granites and nine rhyolites yield zircon 206Pb/238U ages from 262 Ma to 249 Ma, coinciding with the timing of silicic magmatism in the Panxi area of the ELIP. The zircon εHf(t) values (+14 to +3) of these granites and rhyolites suggest a moderately depleted mantle source and overlap with those of peralkaline and metaluminous granites in the Panxi area [i.e. εHf(t) = +14 to +4]. The zircon Hf isotope ratios show that the zircons probably record the original source characteristics whereas whole-rock Nd isotope data indicate an evidence for crustal contamination that may have occurred at lower temperatures during magma emplacement. The synchroneity, coupled with petrological and geochemical similarities, indicate that silicic rocks from the Phan Si Pan-Tu Le region are cogenetic with the Panxi silicic plutonic rocks and that they are likely derived by similar petrogenetic processes (i.e. fractionation of mafic magmas or partial melting of mafic rocks). Therefore, we propose that the Phan Si Pan-Tu Le region represents a displaced portion of the ELIP inner zone.

  5. Mesoporous Silicate Materials in Sensing

    Directory of Open Access Journals (Sweden)

    Paul T. Charles


    Full Text Available Mesoporous silicas, especially those exhibiting ordered pore systems and uniform pore diameters, have shown great potential for sensing applications in recent years. Morphological control grants them versatility in the method of deployment whether as bulk powders, monoliths, thin films, or embedded in coatings. High surface areas and pore sizes greater than 2 nm make them effective as adsorbent coatings for humidity sensors. The pore networks also provide the potential for immobilization of enzymes within the materials. Functionalization of materials by silane grafting or through cocondensation of silicate precursors can be used to provide mesoporous materials with a variety of fluorescent probes as well as surface properties that aid in selective detection of specific analytes. This review will illustrate how mesoporous silicas have been applied to sensing changes in relative humidity, changes in pH, metal cations, toxic industrial compounds, volatile organic compounds, small molecules and ions, nitroenergetic compounds, and biologically relevant molecules.

  6. A Silurian-early Devonian slab window in the southern Central Asian Orogenic Belt: Evidence from high-Mg diorites, adakites and granitoids in the western Central Beishan region, NW China (United States)

    Zheng, Rongguo; Xiao, Wenjiao; Li, Jinyi; Wu, Tairan; Zhang, Wen


    The Beishan orogenic belt is a key region for deciphering the accretionary processes of the southern Central Asian Orogenic Belt. Here in this paper we present new zircon U-Pb ages, bulk-rock major and trace element, and zircon Hf isotopic data for the Baitoushan, and Bagelengtai plutons in the western Central Beishan region to address the accretionary processes. The Baitoushan pluton consists of quartz diorites, monzonites and K-feldspar granites, with zircon LA-ICP-MS U-Pb ages of 435 Ma, 421 Ma and 401 Ma, respectively. The Baitoushan quartz diorites and quartz monzonites exhibit relatively high MgO contents and Mg# values (63-72), display enrichments in LILEs and LREEs, and exhibit high Ba (585-1415 ppm), Sr (416-570 ppm) and compatible element (such as Cr and Ni) abundances, which make them akin to typical high-Mg andesites. The Baitoushan quartz diorites and quartz monzonites were probably generated by the interaction of subducted oceanic sediment-derived melts and mantle peridotites. The Baitoushan K-feldspar granites are ascribed to fractionated I-type granites with peraluminous and high-K calc-alkaline characteristics. They exhibit positive εHf(t) values (2.43-7.63) and Mesoproterozoic-Neoproterozoic zircon Hf model ages (0.92-1.60 Ga). Those early Devonian granites, including Baitoushan K-feldspar granite and Gongpoquan leucogranites (402 Ma), are derived from melting of the mafic lower crust and/or sediments by upwelling of hot asthenospheric mantle. The Bagelengtai granodiorites exhibit similar geochemical signatures with that of typical adakites, with a zircon SHRIMP U-Pb age of 435 Ma. They exhibit relatively high Sr (502-628 ppm) and Al2O3 (16.40-17.40 wt.%) contents, and low MgO (1.02-1.29 wt.%), Y (3.37-6.94 ppm) and HREEs contents, with relatively high Sr/Y and (La/Yb)N ratios. The Bagelengtai granodiorites were derived from partial melting of subducted young oceanic crust, with significant contributions of subducted sediments, subsequently

  7. Mafic dikes at Kahel Tabelbala (Daoura, Ougarta Range, south-western Algeria): New insights into the petrology, geochemistry and mantle source characteristics (United States)

    Mekkaoui, Abderrahmane; Remaci-Bénaouda, Nacéra; Graïne-Tazerout, Khadidja


    New petrological, geochemical and Sr-Nd isotopic data of the Late Triassic and Early Jurassic Kahel Tabelbala (KT) mafic dikes (south-western Algeria) offer a unique opportunity to examine the nature of their mantle sources and their geodynamic significance. An alkaline potassic Group 1 of basaltic dikes displaying relatively high MgO, TiO2, Cr and Ni, La/YbN ∼ 15, coupled with low 87Sr/86Sri ∼ 0.7037 and relatively high ɛNd(t) ∼ +3, indicates minor olivine and clinopyroxene fractionation and the existence of a depleted mantle OIB source. Their parental magma was generated from partial melting in the garnet-lherzolite stability field. A tholeiitic Group 2 of doleritic dikes displaying low MgO, Cr and Ni contents, La/YbN ∼ 5, positive Ba, Sr and Pb anomalies, the absence of a negative Nb anomaly coupled with moderate 87Sr/86Sri ∼ 0.7044 and low ɛNd(t) ∼ 0 (BSE-like), indicates a contamination of a mantle-derived magma that experienced crystal fractionation of plagioclase and clinopyroxene. This second group, similar to the low-Ti tholeiitic basalts of the Central Atlantic Magmatic Province (CAMP), was derived from partial melting in the peridotite source within the spinel stability field. Lower Mesozoic continental rifting could have been initiated by a heterogeneous mantle plume that supplied source components beneath Daoura, in the Ougarta Range.

  8. Pre-1991 sulfur transfer between mafic injections and dacite magma in the Mt. Pinatubo reservoir (United States)

    Di, Muro A.; Pallister, J.; Villemant, B.; Newhall, C.; Semet, M.; Martinez, M.; Mariet, C.


    Before the 1991-1992 activity, a large andesite lava dome belonging to the penultimate Pinatubo eruptive period (Buag ??? 500??BP) formed the volcano summit. Buag porphyritic andesite contains abundant amphibole-bearing microgranular enclaves of basaltic-andesite composition. Buag enclaves have lower K2O and incompatible trace element (LREE, U, Th) contents than mafic pulses injected in the Pinatubo reservoir during the 1991-1992 eruptive cycle. This study shows that Buag andesite formed by mingling of a hot, water-poor and reduced mafic magma with cold, hydrous and oxidized dacite. Depending on their size, enclaves experienced variable re-equilibration during mixing/mingling. Re-equilibration resulted in hydration, oxidation and transfer of mobile elements (LILE, Cu) from the dacite to the mafic melts and prompted massive amphibole crystallization. In Buag enclaves, S-bearing phases (sulfides, apatite) and melt inclusions in amphibole and plagioclase record the evolution of sulfur partition among melt, crystal and fluid phases during magma cooling and oxidation. At high temperature, sulfur is partitioned between andesitic melt and sulfides (Ni-pyrrhotite). Magma cooling, oxidation and hydration resulted in exsolution of a S-Cl-H2O vapor phase at the S-solubility minimum near the sulfide-sulfate redox boundary. Primary magmatic sulfide (pyrrhotite) and xenocrystic sulfide grains (pyrite), recycled together with olivines and pyroxenes from old mafic intrusives, were replaced by Cu-rich phases (chalcopyrite, cubanite) and, partially, by Ba-Sr sulfate. Sulfides degassed and transformed into residual spongy magnetite in response to fS2 drop during final magma ascent and decompression. Our research suggests that a complete evaluation of the sulfur budget at Pinatubo must take into account the en route S assimilation from the country rocks. Moreover, this study shows that the efficiency of sulfur transfer between mafic recharges and injected magmas is controlled by the

  9. Mafic sill/dykes intruding into late Maastrichtian-early Paleocene calciclastic units, NE-Turkey: Petrographical and geochemical features of latest magmatic activity before collision in the eastern Sakarya zone (United States)

    Aydin, Faruk; Oǧuz, Simge; Karsli, Orhan; Kandemir, Raif; Şen, Cüneyt; Uysal, İbrahim


    We present here new petrographical, mineralogical and whole-rock geochemical data for mafic sill/dykes intruding into late Maastrichtian-early Paleocene calciclastic units in the Düzköy (Trabzon) and Cankurtaran (Artvin) areas (NE Turkey) of the eastern Sakarya zone (ESZ) in order to decipher the latest magmatic activity in the final stage of subduction-related magmatism of the ESZ. U-Pb zircon dating for the mafic sill/dykes in the region yielded ages varying from 83.6 to 78.5Ma (i.e. Early Campanian). Mafic sill/dykes consist of mostly basalts and lesser basaltic-andesites with komatiitic basalts. Most of the dyke samples display aphyric to porphyritic texture with phenocrysts of plagioclase (mostly replaced by calcite), clinopyroxene (partly uralized), olivine (almost serpentinized), and amphibole (partly chloritized). Based on the MgO, Nb and Zr contents with Nb/Y ratio, the mafic dykes from Düzköy area are mainly classified as two subgroups (basalts and basaltic andesites) while those of Cankurtaran can be divided into three different groups (low- and high-Nb normal basalts and komatitic basalts). Düzköy basaltic dykes have higher MgO (3.8-7.8%) and lower Nb (3-4ppm) and Zr (53-62ppm) contents with Nb/Y ratio (˜0.2) than those of Düzköy basaltic-andesitic dykes (MgO: ˜1.8%, Nb: 6-15ppm, Zr: 106-145ppm, Nb/Y: 0.3-0.6). On the other hand, Cankurtaran mafic sill/dykes have relatively high MgO contents (˜4-20%). These sill/dykes with 15-20% of MgO and contents are called as komatiitic basalt which has relatively low K2O (contents with Nb/Y ratio (˜0.1-0.2). However, normal basalts from Cankurtaran have quite lower MgO contents (˜4-9%) than that of the komatiitic basalt. Also, they can be divided into two subgroups in terms of MgO (5.7-8.7% for group 1 and 4.0-4.4% for group 2), Nb (3-14ppm for group 1 and 19-21ppm for group 2), Zr (94-111ppm for group 1 and 125-140ppm for group 2) contents, and Nb/Y ratio (˜0.2-0.8 for group 1 and (˜1.0-1.2 for

  10. Alkali Silicate Vehicle Forms Durable, Fireproof Paint (United States)

    Schutt, John B.; Seindenberg, Benjamin


    The problem: To develop a paint for use on satellites or space vehicles that exhibits high resistance to cracking, peeling, or flaking when subjected to a wide range of temperatures. Organic coatings will partially meet the required specifications but have the inherent disadvantage of combustibility. Alkali-silicate binders, used in some industrial coatings and adhesives, show evidence of forming a fireproof paint, but the problem of high surface-tension, a characteristic of alkali silicates, has not been resolved. The solution: Use of a suitable non-ionic wetting agent combined with a paint incorporating alkali silicate as the binder.

  11. Model Dust Envelopes Around Silicate Carbon Stars

    Directory of Open Access Journals (Sweden)

    Kyung-Won Suh


    Full Text Available We have modeled dust envelopes around silicate carbon stars using optical properties for a mixture of amorphous carbon and silicate dust grains paying close attention to the infrared observations of the stars. The 4 stars show various properties in chemistry and location of the dust shell. We expect that the objects that fit a simple detached silicate dust shell model could be in the transition phase of the stellar chemistry. For binary system objects, we find that a mixed dust chemistry model would be necessary.

  12. Integrated Experimental and Modeling Studies of Mineral Carbonation as a Mechanism for Permanent Carbon Sequestration in Mafic/Ultramafic Rocks

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Zhengrong [Yale Univ., New Haven, CT (United States); Qiu, Lin [Yale Univ., New Haven, CT (United States); Zhang, Shuang [Yale Univ., New Haven, CT (United States); Bolton, Edward [Yale Univ., New Haven, CT (United States); Bercovici, David [Yale Univ., New Haven, CT (United States); Ague, Jay [Yale Univ., New Haven, CT (United States); Karato, Shun-Ichiro [Yale Univ., New Haven, CT (United States); Oristaglio, Michael [Yale Univ., New Haven, CT (United States); Zhu, Wen-Iu [Univ. of Maryland, College Park, MD (United States); Lisabeth, Harry [Univ. of Maryland, College Park, MD (United States); Johnson, Kevin [Univ. of Hawaii, Honolulu, HI (United States)


    A program of laboratory experiments, modeling and fieldwork was carried out at Yale University, University of Maryland, and University of Hawai‘i, under a DOE Award (DE-FE0004375) to study mineral carbonation as a practical method of geologic carbon sequestration. Mineral carbonation, also called carbon mineralization, is the conversion of (fluid) carbon dioxide into (solid) carbonate minerals in rocks, by way of naturally occurring chemical reactions. Mafic and ultramafic rocks, such as volcanic basalt, are natural candidates for carbonation, because the magnesium and iron silicate minerals in these rocks react with brines of dissolved carbon dioxide to form carbonate minerals. By trapping carbon dioxide (CO2) underground as a constituent of solid rock, carbonation of natural basalt formations would be a secure method of sequestering CO2 captured at power plants in efforts to mitigate climate change. Geochemical laboratory experiments at Yale, carried out in a batch reactor at 200°C and 150 bar (15 MPa), studied carbonation of the olivine mineral forsterite (Mg2SiO4) reacting with CO2 brines in the form of sodium bicarbonate (NaHCO3) solutions. The main carbonation product in these reactions is the carbonate mineral magnesite (MgCO3). A series of 32 runs varied the reaction time, the reactive surface area of olivine grains and powders, the concentration of the reacting fluid, and the starting ratio of fluid to olivine mass. These experiments were the first to study the rate of olivine carbonation under passive conditions approaching equilibrium. The results show that, in a simple batch reaction, olivine carbonation is fastest during the first 24 hours and then slows significantly and even reverses. A natural measure of the extent of carbonation is a quantity called the carbonation fraction, which compares the amount of carbon removed from solution, during a run, to the maximum amount

  13. Paleomagnetic record of a geomagnetic field reversal from late miocene mafic intrusions, southern nevada. (United States)

    Ratcliff, C D; Geissman, J W; Perry, F V; Crowe, B M; Zeitler, P K


    Late Miocene (about 8.65 million years ago) mafic intrusions and lava flows along with remagnetized host rocks from Paiute Ridge, southern Nevada, provide a high-quality paleomagnetic record of a geomagnetic field reversal. These rocks yield thermoremanent magnetizations with declinations of 227 degrees to 310 degrees and inclinations of -7 degrees to 49 degrees , defining a reasonably continuous virtual geomagnetic pole path over west-central Pacific longitudes. Conductive cooling estimates for the intrusions suggest that this field transition, and mafic magmatism, lasted only a few hundred years. Because this record comes principally from intrusive rocks, rather than sediments or lavas, it is important in demonstrating the longitudinal confinement of the geomagnetic field during a reversal.

  14. Ultramafic lavas and pyroxene-spinifex high-Mg basaltic dykes from the Othris ophiolite complex, Greece (United States)

    Baziotis, Ioannis; Economou-Eliopoulos, Maria; Asimow, Paul


    This study aims to constrain the physico-chemical conditions and processes associated with the origin of ultramafic lavas of the Agrilia formation and high-Mg basaltic dykes in the Pournari area within the Othris ophiolite complex, a supra-subduction zone ophiolite of Mesozoic age (Paraskevopoulos & Economou, 1986; Barth et al., 2008). Hand-sample-scale spinifex texture is lacking from the ultramafic lavas and, despite whole-rock MgO contents greater than 31 wt.%, we infer an upper bound of 17 wt.% MgO for the erupted liquid, and thus identify these lavas as picrites containing accumulated olivine. We use textural and compositional criteria to divide the crystals within the Agrilia lavas between pre-eruptive and post-eruptive growth phases. The high-Mg basaltic dyke margins display a distinctive thin-section-scale micro-spinifex texture of skeletal and plumose Al- and Fe-rich clinopyroxene surrounded by large crystals of orthopyroxene. Normally zoned clinopyroxene in the Agrilia lavas and clinopyroxene of various textures (skeletal, needle- and dendritic-like) and sizes in the Pournari dykes display anomalous enrichment in Al2O3 and FeO* with decreasing MgO that require rapid, disequilibrium growth. Quantitative characteristics of the micro-spinifex pyroxene textures (Elements and related metals are Pd/Ir=11.5-13.0, Cu/Pd=6000-7210, Ti/Pd=22.78-31.97×103 for Agrilia lavas and Pd/Ir=4.5-14.0, Cu/Pd=3140-5550, Ti/Pd=4.66-17.32×103 for Pournari dykes; all are very close to those reported for typical komatiites (Barnes et al., 1988). Despite the absence of true komatiite lavas, a number of geochemical features of the Othris suite, including the PGE contents and ratios and the micro-spinifex, disequilibrium cpx growth, are similar to Mesozoic and Archaean komatiites. References Barnes et al., 1988. Journal of Petrology 29, 305-331. Barth et al., 2008. Lithos, 100(1), 234-254. Faure et al., 2006. Journal of Petrology 47, 1591- 1610. Paraskevopoulos, G., Economou, M

  15. Silicate and Carbonatite Melts in the Mantle: Adding CO2 to the pMELTS Thermodynamic Model of Silicate Phase Equilibria (United States)

    Antoshechkina, P. M.; Shorttle, O.


    The current rhyolite-MELTS algorithm includes a mixed H2O-CO2 vapor phase, and a self-consistent speciation model for CO2 and CaCO3 in the silicate liquid (Ghiorso & Gualda 2012; 2015). Although intended primarily to model crustal differentiation and degassing, GG15 captures much of the experimentally-observed melting behavior of CO2-rich mafic lithologies, including generation of small-degree carbonatite melts, a miscibility gap between carbonatite and silicate liquids at low P and a smooth transition to a single carbonated-silicate melt at high P (e.g. Dasgupta et al. 2007). However, solid and liquid carbonate phases were not used in calibration of GG15, and it is suitable only for P MySQL database, adapted from LEPR (Hirschmann et al. 2008). Here, we further extend our database, e.g. to include multiple carbonate phases, and combine the calibration scheme with the libalphaMELTS interface to the rhyolite-MELTS, pMELTS, and H2O-CO2 fluid thermodynamic models (see We use a Monte-Carlo type calibration approach to fit the observed phases and compositions, though stop short of a fully Bayesian formulation. The CO2-fluid experimental database has been updated to include more recent and higher P studies, adding approximately 40 pure fluid plus liquid constraints that conform to the selection criteria used in GG15. To further expand the database, we plan to use some or all of: solid carbonate-bearing experiments; coexisting silicate and carbonatite liquids; phase-present, and phase-absent constraints. As a first approximation, we include four carbonate phases: pure calcite and aragonite, and binary solutions for dolomite-ankerite and magnesite-siderite. Following GG15, we have adopted the CO2 fluid model of Duan & Zhang (2006) and added CO2 and CaCO3 species to the pMELTS liquid model. A key question that we hope to address during calibration is whether a Na2CO3 liquid species is justified instead of, or in addition to, CaCO3 for the

  16. Siliceous microfossil extraction from altered Monterey rocks

    Energy Technology Data Exchange (ETDEWEB)

    Nelson, C.O.; Casey, R.E.


    Samples of altered Monterey rocks of differing lithologies were processed by various methods to develop new techniques for extracting siliceous microfossils. The preliminary use of thin sections made from the same rocks reduced the number of probable samples (samples worth further processing) by about one-third. Most of the siliceous microfossils contained in altered Monterey rocks appear to be highly recrystallized and are extremely fragile; however, some contained silicified and silica-infilled radiolarians and planktonic and benthonic foraminifera, which are very tough. In general the most useful techniques were gently hydrochloric acid, hydrogen peroxide, formic acid, monosodium glutamate, and regular siliceous microfossil extraction techniques. Unsuccessful techniques and a new siliceous microfossil flotation technique are also documented.

  17. Carbon Monoxide Silicate Reduction System Project (United States)

    National Aeronautics and Space Administration — The Carbon Monoxide Silicate Reduction System (COSRS) is a novel technology for producing large quantities of oxygen on the Moon. Oxygen yields of 15 kilograms per...

  18. Carbon Monoxide Silicate Reduction System Project (United States)

    National Aeronautics and Space Administration — The Carbon Monoxide Silicate Reduction System (COSRS) is an innovative method that for the first time uses the strong reductant carbon monoxide to both reduce iron...

  19. Petrogenesis and geodynamic significance of silicic volcanism in the western Trans-Mexican Volcanic Belt (United States)

    Petrone, C. M.; Ferrari, L.; Orozco, M. A.; Lopez Martinez, M.


    produced pulses of mafic magma that were partly trapped in the crust yielding crustal melting. Extensional faulting since the Pliocene favours the eruption of silicic magma as effusive dome and lava flows. Rifting at the boundaries of the Jalisco block is seen as a rollback induced reactivation of crustal structures but is unlike to evolve into a Jalisco microplate.

  20. Peralkaline silicic volcanic rocks in northwestern nevada. (United States)

    Noble, D C; Chipman, D W; Giles, D L


    Late Tertiary silicic ashflow tuffs and lavas peralkaline in chemical character (atomic Na + K greater than Al), mainly comendites, occur over wide areas in northwestern Nevada and appear to be widespread in southeastern Oregon. Such peralkaline rocks-which are not uncommon in the western United States-and other chemically unusual silicic rocks are found near the margins rather than toward the center of the Great Basin.

  1. Postcollisional mafic igneous rocks record crust-mantle interaction during continental deep subduction. (United States)

    Zhao, Zi-Fu; Dai, Li-Qun; Zheng, Yong-Fei


    Findings of coesite and microdiamond in metamorphic rocks of supracrustal protolith led to the recognition of continental subduction to mantle depths. The crust-mantle interaction is expected to take place during subduction of the continental crust beneath the subcontinental lithospheric mantle wedge. This is recorded by postcollisional mafic igneous rocks in the Dabie-Sulu orogenic belt and its adjacent continental margin in the North China Block. These rocks exhibit the geochemical inheritance of whole-rock trace elements and Sr-Nd-Pb isotopes as well as zircon U-Pb ages and Hf-O isotopes from felsic melts derived from the subducted continental crust. Reaction of such melts with the overlying wedge peridotite would transfer the crustal signatures to the mantle sources for postcollisional mafic magmatism. Therefore, postcollisonal mafic igneous rocks above continental subduction zones are an analog to arc volcanics above oceanic subduction zones, providing an additional laboratory for the study of crust-mantle interaction at convergent plate margins.

  2. Physical abrasion of mafic minerals and basalt grains: application to Martian aeolian deposits (United States)

    Cornwall, Carin; Bandfield, Joshua L.; Titus, Timothy N.; Schreiber, B. C.; Montgomery, D.R.


    Sediment maturity, or the mineralogical and physical characterization of sediment deposits, has been used to locate sediment source, transport medium and distance, weathering processes, and paleoenvironments on Earth. Mature terrestrial sands are dominated by quartz, which is abundant in source lithologies on Earth and is physically and chemically stable under a wide range of conditions. Immature sands, such as those rich in feldspars or mafic minerals, are composed of grains that are easily physically weathered and highly susceptible to chemical weathering. On Mars, which is predominately mafic in composition, terrestrial standards of sediment maturity are not applicable. In addition, the martian climate today is cold, dry and sediments are likely to be heavily influenced by physical weathering rather than chemical weathering. Due to these large differences in weathering processes and composition, martian sediments require an alternate maturity index. Abrason tests have been conducted on a variety of mafic materials and results suggest that mature martian sediments may be composed of well sorted, well rounded, spherical basalt grains. In addition, any volcanic glass present is likely to persist in a mechanical weathering environment while chemically altered products are likely to be winnowed away. A modified sediment maturity index is proposed that can be used in future studies to constrain sediment source, paleoclimate, mechanisms for sediment production, and surface evolution. This maturity index may also provide details about erosional and sediment transport systems and preservation processes of layered deposits.

  3. Thermodynamics and Kinetics of Silicate Vaporization (United States)

    Jacobson, Nathan S.; Costa, Gustavo C. C.


    Silicates are a common class of materials that are often exposed to high temperatures. The behavior of these materials needs to be understood for applications as high temperature coatings in material science as well as the constituents of lava for geological considerations. The vaporization behavior of these materials is an important aspect of their high temperature behavior and it also provides fundamental thermodynamic data. The application of Knudsen effusion mass spectrometry (KEMS) to silicates is discussed. There are several special considerations for silicates. The first is selection of an appropriate cell material, which is either nearly inert or has well-understood interactions with the silicate. The second consideration is proper measurement of the low vapor pressures. This can be circumvented by using a reducing agent to boost the vapor pressure without changing the solid composition or by working at very high temperatures. The third consideration deals with kinetic barriers to vaporization. The measurement of these barriers, as encompassed in a vaporization coefficient, is discussed. Current measured data of rare earth silicates for high temperature coating applications are discussed. In addition, data on magnesium-iron-silicates (olivine) are presented and discussed.

  4. Pre-Elsonian mafic magmatism in the Nain Igneous Complex, Labrador: the bridges layered intrusion (United States)

    Ashwal, L.D.; Wiebe, R.A.; Wooden, J.L.; Whitehouse, M.J.; Snyder, Diane


    Decades of work on the pristine, unmetamorphosed, and well exposed anorthositic, mafic and granitic rocks of the Nain igneous complex, Labrador, have led to the conclusion that all plutonic rocks in that area were emplaced in a short time intercal at about 1300 ?? 10 Ma). We report here new isotopic data for mafic intrusive rocks that appear to have crystallized several hundred Ma earlier than the bulk of the plutonic activity in the Nain complex. The Bridges layered intrusion (BLI) is a small (15-20 km2) lens of layered mafic rocks about 1.5 km thick, surrounded and intruded by anorthositic, leuconoritic and leucotroctolitic plutons in the middle of the coastal section of the Nain igneous complex. BLI shows very well developed magmatic structures, including channel scours, slump structures, and ubiquitous modally graded layering. Most rocks, however, show granular textures indicative of recrystallization, presumably caused by emplacement of younger anorthositic rocks. BLI contains cumulate rocks with slightly more primitive mineral compositions (An60-83, Fo66-71) than those of other mafic intrusions in the Nain igneous complex, including Kiglapait. SmNd isotopic data for 7 BLI whole-rocks ranging in composition between olivine melagabbro and olivine leucogabbro yield an age of 1667 ?? 75 Ma, which we interpret as the time of primary crystallization. The internal isotopic systematics of the BLI have been reset, probably by intrusion of adjacent anorthositic plutons. A SmNd mineral isochron (plag, whole-rock, mafics) for a BLI olivine melagabbro gives an age of 1283 ?? 22 Ma, equivalent within error of a mineral array (plag, whole-rock, opx, cpx) for an adjacent, igneous-textured, leuconorite vein (1266 ?? 152 Ma). The initial Nd ratio for BLI corresponds to ??{lunate}Nd = -3.18 ?? 0.44. Other whole-rock samples, however, some with vein-like alteration (Chlorite, serpentine, amphiboles), show ??{lunate}Nd values as low as -9.1, suggesting variable contamination by

  5. 40Ar/39Ar chronology and volcanology of silicic volcanism in the Davis Mountains, Trans-Pecos Texas (United States)

    Henry, Christopher D.; Kunk, M.J.; McIntosh, W.C.


    probably in the western Davis Mountains.Intermediate and mafic rocks are minor, except around the southeastern flank of the Davis Mountains, where basalt is abundant. Mafic lavas erupted only during gaps in the silicic activity and on the flanks of the Davis Mountains. Nevertheless, basaltic magma probably drove the silicic magmatism, either by differentiation or by crustal melting, and was present throughout the time of Davis Mountains activity but could not penetrate the low-density silicic magma chambers until they cooled and solidified. The time required for cooling and solidification appears to be 0.1-0.2 m.y.

  6. Hydrothermal Synthesis of Dicalcium Silicate Based Cement (United States)

    Dutta, N.; Chatterjee, A.


    It is imperative to develop low energy alternative binders considering the large amounts of energy consumed as well as carbon dioxide emissions involved in the manufacturing of ordinary Portland cement. This study is on the synthesis of a dicalcium silicate based binder using a low temperature hydrothermal route.The process consists of synthesizing an intermediate product consisting of a calcium silicate hydrate phase with a Ca:Si ratio of 2:1 and further thermal treatment to produce the β-Ca2SiO4 (C2S) phase.Effect of various synthesis parameters like water to solid ratio, dwell time and temperature on the formation of the desired calcium silicate hydrate phase is reported along with effect of heating conditions for formation of the β-C2S phase. Around 77.45% of β-C2S phase was synthesized by thermal treatment of the intermediate phase at 820°C.

  7. The Breccia of Frog Lakes: Record of Mafic Arc Magmatism in the Mesozoic Sierra Nevada, California (United States)

    Douglas, S.; Riggs, N.; Barth, A. P.; Economos, R. C.


    The evolution of the Mesozoic western margin of North America in California is characterized by a change in tectonic regimes. After the emplacement of the Golconda thrust during the Sonoma orogeny in early Triassic time, the passive western margin changed to a convergent margin with subducting oceanic crust. Onset of arc magmatism is recorded by the volcanic section of Saddlebag Lake pendant in the east-central Sierra Nevada and includes welded tuffs, mafic flows, and volcanic breccias. The welded tuffs and mafic breccias provide insight into the diversity of volcanic processes during early evolution of the Sierran arc. The Mesozoic volcanic section of the Saddlebag Lake pendant (SLP) overlies foreland basin sediments derived from the eroding Golconda allochthon. The initial volcanic unit, the tuff of Black Mountain, is overlain by the conglomerate of Cooney Lake, which contains continental-derived sediment similar to the Candelaria Fm, and no volcanic clasts. Stratigraphically above the conglomerate is the 224 Ma tuff of Saddlebag Lake, which underlies the breccia of Frog Lakes. The breccia of Frog Lakes thus represents the earliest stratigraphic record of mafic volcanism in the Mesozoic Sierran arc. Basaltic to andesitic clasts found within the breccia of Frog Lakes are geochemically similar to modern arc-derived andesites, enriched in fluid-mobile LILEs, indicating that water had been introduced into the mantle wedge by the subducting plate and consequently depleted in less-mobile HFSEs, especially niobium. A subaqueous setting is indicated by the presence of a fine-grained, laminated sedimentary succession between the tuff of Saddlebag Lake and the breccia of Frog Lakes, together with jigsaw fragmentation of Frog Lakes breccia clasts, fluidal margins of some of these clasts, and localized fine-grained laminated sedimentary zones within clast-rich horizons. Although the arc setting remained subaqueous throughout deposition of at least the basal SLP Mesozoic

  8. Dihedral Angles As A Diagnostic Tool For Interpreting The Cooling History Of Mafic Rocks (United States)

    Holness, M. B.


    The geometry of three-grain junctions in mafic rocks, particularly those involving two grains of plagioclase, overwhelmingly results from processes occurring during solidification. Sub-solidus textural modification is only significant for fine-grained rocks that have remained hot for a considerable time (e.g. chill zones). The underlying control on the geometry of junctions involving plagioclase is the response of the different plagioclase growth faces to changes in cooling rate. This is demonstrated by the systematic co-variation of plagioclase grain shape and the median value of the pyroxene-plag-plag dihedral angle across (unfractionated) mafic sills. In mafic layered intrusions the median dihedral angle is constant across large stretches of stratigraphy, changing in a step-wise manner as the number of liquidus phases changes in the bulk magma. In the Skaergaard layered intrusion, the shape of cumulus plagioclase grains changes smoothly through the stratigraphy, consistent with continuously decreasing cooling rates in a well-mixed chamber: there is no correlation between overall plagioclase grain shape and dihedral angle. However, three-grain junctions are formed during the last stages of crystallization and therefore record events at the base of the crystal mushy layer. While the overall shape of plagioclase grains is dominated by growth at the magma-mush interface or in the bulk magma, it is the post-accumulation overgrowth that creates the dihedral angle: the shape of this overgrowth changes in a step-wise fashion, matching the step-wise variation in dihedral angle. Dihedral angles in layered intrusions can be used to place constraints on the thickness of the mushy layer, using the stratigraphic offset between the step-wise change in dihedral angle and the first appearance/disappearance of the associated liquidus phase. Dihedral angles also have the potential to constrain intrusion size for fragments of cumulate rocks entrained in volcanic ejecta.

  9. Silicate mineral dissolution during heap bioleaching. (United States)

    Dopson, Mark; Halinen, Anna-Kaisa; Rahunen, Nelli; Boström, Dan; Sundkvist, Jan-Eric; Riekkola-Vanhanen, Marja; Kaksonen, Anna H; Puhakka, Jaakko A


    Silicate minerals are present in association with metal sulfides in ores and their dissolution occurs when the sulfide minerals are bioleached in heaps for metal recovery. It has previously been suggested that silicate mineral dissolution can affect mineral bioleaching by acid consumption, release of trace elements, and increasing the viscosity of the leach solution. In this study, the effect of silicates present in three separate samples in conjunction with chalcopyrite and a complex multi-metal sulfide ore on heap bioleaching was evaluated in column bioreactors. Fe(2+) oxidation was inhibited in columns containing chalcopyrite samples A and C that leached 1.79 and 1.11 mM fluoride, respectively but not in sample B that contained 0.14 mM fluoride. Microbial Fe(2+) oxidation inhibition experiments containing elevated fluoride concentrations and measurements of fluoride release from the chalcopyrite ores supported that inhibition of Fe(2+) oxidation during column leaching of two of the chalcopyrite ores was due to fluoride toxicity. Column bioleaching of the complex sulfide ore was carried out at various temperatures (7-50 degrees C) and pH values (1.5-3.0). Column leaching at pH 1.5 and 2.0 resulted in increased acid consumption rates and silicate dissolution such that it became difficult to filter the leach solutions and for the leach liquor to percolate through the column. However, column temperature (at pH 2.5) only had a minor effect on the acid consumption and silicate dissolution rates. This study demonstrates the potential negative impact of silicate mineral dissolution on heap bioleaching by microbial inhibition and liquid flow. Copyright 2007 Wiley Periodicals, Inc.

  10. Study on the formation process of composite MMEs (mafic magmatic enclaves) in Taejongdae, Busan Korea. (United States)

    Adam, Mohammed; Kim, Young-Seog; Kim, Taehyung


    Mafic Magmatic Enclave (MME) is a common feature in granitic rocks. However, the layered MMEs developed in the outcrop of Cretaceous granite in Taejongdae National Geopark, Busan show various patterns and interesting phenomena providing useful information on the formation of MMEs. We define here the layered MME as MME composed of several contrasting rock shells. Characteristics and origin of MMEs have been studied in several ways; descriptively, geochemically and through isotope studies due to their importance in the evolution of igneous rocks. This study aims to understand the formation mechanism of the composite MMEs, including the reasons for the diversity of the MME rock types. To achieve those tasks, the relationship between the MMEs and the host granite, and difference between the layers were investigated based on petrological, XRF and EPMA analyses. The important results include the followings: the MMEs can be categorized into two main types; Simple-type composed of a single rock type, and Layered-type composed of different surrounded rock shells. Most of the Simple-type have relatively angular shapes and small sizes, and their contacts with the host granite are commonly sharp but some show small dioritic mixing rims. The forming rocks of the simple MMEs are variable from mafic porphyritic, mafic fine to medium grains and felsic coarse-grained dioritic rocks. The layered MMEs have almost circular to elliptical shapes, and show gradual change in composition from mafic and porphyritic texture in the center to fine in the outer shells (like a chilled margin) and again surrounded by a dioritic layer. The dioritic layer shows another chilled margin with the host granite, indicating double cooling mechanism. Some MMEs are injected by granitic materials through cracks. The injection of the granitic materials into the layered MMEs may indicate fracturing during the cooling process. They may indicate two different phases of mingling and one phase of mixing event. The

  11. Nanostructure of Calcium Silicate Hydrates in Cements

    KAUST Repository

    Skinner, L. B.


    Calcium silicate hydrate (CSH) is the major volume phase in the matrix of Portland cement concrete. Total x-ray scattering measurements with synchrotron x rays on synthetic CSH(I) shows nanocrystalline ordering with a particle diameter of 3.5(5) nm, similar to a size-broadened 1.1 nm tobermorite crystal structure. The CSH component in hydrated tricalcium silicate is found to be similar to CSH(I). Only a slight bend and additional disorder within the CaO sheets is required to explain its nanocrystalline structure. © 2010 The American Physical Society.

  12. Quantitative EPMA Compositional Mapping of NWA 2995: Characterization, and Petrologic Interpretation of Mafic Clasts (United States)

    Carpenter, P. K.; Hahn, T. M.; Korotev, R. L.; Ziegler, R. A.; Jolliff, B. L.


    We present the first fully quantitative compositional maps of lunar meteorite NWA 2995 using electron microprobe stage mapping, and compare selected clast mineralogy and chemistry. NWA 2995 is a feldspathic fragmental breccia containing numerous highland fine grained lithologies, including anorthosite, norite, olivine basalt, subophitic basalt, gabbro, KREEP-like basalt, granulitic and glassy impact melts, coarse-grained mineral fragments, Fe-Ni metal, and glassy matrix [1]. Chips of NWA 2995, representing these diverse materials, were analyzed by INAA and fused-bead electron-probe microanalysis (EPMA); comparison of analytical data suggests grouping of lunar meteorites NWA 2995, 2996, 3190, 4503, 5151, and 5152. The mean composition of NWA 2995 corresponds to a 2:1 mixture of feldspathic and mare material, with approximately 5% KREEP component [2]. Clast mineral chemistry and petrologic interpretation of paired stone NWA 2996 has been reported by Mercer et al. [3], and Gross et al. [4]. This study combines advances in quantitative EPMA compositional mapping and data analysis, as applied to selected mafic clasts in a polished section of NWA 2995, to investigate the origin of mafic lithic components and to demonstrate a procedural framework for petrologic analysis.

  13. Hydrogeochemistry of deep groundwaters of mafic and ultramafic rocks in Finland

    Energy Technology Data Exchange (ETDEWEB)

    Ruskeeniemi, T.; Blomqvist, R.; Lindberg, A.; Ahonen, L. [Geological Survey of Finland, Espoo (Finland); Frape, S. [Waterloo Univ., ON (Canada)


    The present work reports and interprets the hydrogeochemical and hydrogeological data obtained from deep groundwaters in various mafic-ultramafic formations in Finland. The work is mainly based on the results of the research project `Geochemistry of deep groundwaters` financed by the Ministry of Trade and Industry and the Geological Survey of Finland. Five sites were selected for this study: (1) Juuka, (2) Keminmaa, (3) Maentsaelae, (4) Ranua, and (5) Ylivieska. Keminmaa and Ranua are located in Early Proterozoic layered intrusions dated at 2.44 Ga. The Juuka site lies within the massive Miihkali serpentinite, which is thought to represent the ultramafic part of a Proterozoic (1.97 Ga) ophiolite complex. The Maentsaelae gabbro represents the deep parts of the Svecofennian volcanic sequence, while the Ylivieska mafic-ultramafic intrusion is one of a group of Svecokarelian Ni-potential intrusions 1.9 Ga in age. For reference, groundwaters from four other sites are also briefly described. Three of these sites are located within the nickel mining regions of Enonkoski, Kotalahti and Vammala, while the fourth is a small Ni mineralization at Hyvelae, Noormarkku. The four reference sites are all of Svecokarelian age. (refs.).

  14. Stability constants for silicate adsorbed to ferrihydrite

    DEFF Research Database (Denmark)

    Hansen, Hans Christian Bruun; Wetche, T.P.; Raulund-Rasmussen, Karsten


    Intrinsic surface acidity constants (K(a1)intr, K(a2)intr) and surface complexation constant for adsorption of orthosilicate onto synthetic ferrihydrite (K(Si) for the complex = FeOSi(OH)3) have been determined from acid/base titrations in 0.001-0.1 m NaClO4 electrolytes and silicate adsorption e...

  15. Combustion synthesis and photoluminescence study of silicate ...

    Indian Academy of Sciences (India)

    Silicate based bioceramics are promising candidates as biomaterials for tissue engineering. The combustion synthesis method provides control on the morphology and particle size of the synthesized material. This paper discusses the combustion synthesis of akermanite (Ca2MgSi2O7 and Sr2MgSi2O7), which has been ...

  16. Suppressive effects of a polymer sodium silicate solution on ...

    African Journals Online (AJOL)

    The silicon contents in the roots of the miniature rose treated with polymer sodium silicate were significantly greater than that in plants treated with monomer sodium silicate. In conclusion, the suppressive effects of sodium silicate in the polymer form were confirmed against powdery mildew and root rot diseases of the ...

  17. The role of water in silicate oligomerization reaction

    NARCIS (Netherlands)

    Trinh, T.T.; Jansen, A.P.J.; Santen, R.A.; Meijer, E.J.


    The silicate oligomerization reaction is key to sol-gel chemistry and zeolite synthesis. Numerous experimental and theoretical studies have been devoted to investigating the physical chemistry of silicate oligomers in the prenucleation stage of siliceous zeolite formation. Most of the previous

  18. Suppressive effects of a polymer sodium silicate solution on ...

    African Journals Online (AJOL)



    Oct 21, 2015 ... Sodium silicate was dissolved in water in either a monomer form or polymer form; the effects of both forms of sodium silicate aqueous solution on rose powdery mildew and root rot diseases of miniature rose were examined. Both forms of sodium silicate aqueous solution were applied to the roots of the.

  19. Petrogenesis and timing of mafic magmatism, South Taimyr, Arctic Siberia: A northerly continuation of the Siberian Traps? (United States)

    Reichow, M. K.; Saunders, A. D.; Scott, R. A.; Millar, I. L.; Barfod, D.; Pringle, M. S.; Rogers, N. W.; Hammond, S.


    The Siberian large igneous province (LIP) forms the world's most extensive continental exposure of basalt and has several sub-provinces surrounding it, which may be genetically related. The Taimyr peninsula of north Siberia is one of these sub-provinces and is frequently assumed to be the northerly continuation of the basalts exposed at Noril'sk, the best-studied area of the Siberian LIP. However, the correlation is uncertain. We present new major and trace element data from 35 samples of extrusive and intrusive rocks from Taimyr, with Sr and Nd isotope data from a subset of ten. The Taimyr rocks fall into two groups with low (~ 7 wt.%) and elevated (~ 9 wt.%) MgO concentrations. The high-MgO rocks display a restricted range of initial 87Sr/86Sr (0.705 to 0.706) and 143Nd/144Nd (0.5122 to 0.5124) ratios, and share bulk silicate earth normalised rare earth element patterns strikingly similar to data observed in the ore-related Noril'sk intrusions. The remaining low-MgO group samples have a broader range with higher Sr and lower Nd isotope values and higher incompatible trace element ratios (e.g., Th/Ta > 5.3 and La/Smn > 1.7) similar to the crustally-contaminated Nadezhdinsky and Morongovsky suite basalts of the Noril'sk region. The major and trace element data for both groups are consistent with a process of fractional crystallisation coupled with small degrees of assimilation of incompatible-element-enriched lower crust involving different contaminants. Trace element model calculations indicate a process of magma formation at large degrees of partial melting and at pressures of less than 3 GPa, probably within the garnet-spinel transition zone or the spinel stability field of the asthenospheric mantle. We obtained an argon plateau age of ~ 252 (252.7 ± 1.5) Ma and a ~ 239 Ma total fusion age from a Taimyr lava and intrusive sample, respectively, confirming that volcanism is only partly contemporaneous with the activity of the Siberian LIP. Although this is in

  20. Rheological property of mafic schist and geological interpretation to the subduction dynamics (United States)

    Okazaki, K.; Hirth, G.


    To understand the spatial and temporal distribution of deformation (e.g., underplating and exhumation of metamorphic rocks) and earthquakes in subduction zones, it is important to constrain the rheological properties of metamorphic rocks (i.e., altered oceanic crust and sediments), and how they evolve during metamorphic reactions following hydration, carbonation and dehydration of the down-going slab. Metamorphism of oceanic crust has stimulated hypotheses on the relationship between intra-slab earthquakes and slab-wedge coupling along plate boundaries in subduction zone. While it is well known that metamorphisms have important effects on material circulation and arc volcanisms at subduction system, it remains unclear how the formation of metamorphic minerals followed by fluid release on the subduction dynamics influences rheology. Past experimental studies on mafic metamorphic rocks were mostly concentrated on phase equilibrium of mineral, thus there are very few reports on the mechanical data for these metamorphic rocks. We conducted triaxial deformation experiments on a mafic greenschist using Griggs-type solid pressure-medium apparatus installed in Brown University. Mafic schist (chlorite - amphibole - epidote - albite schist) containing calcite and quartz veins from Sambagawa metamorphic belt (Japan), which is metamorphosed at the condition of nearly the corner of mantle wedge in hot subduction (1 GPa of pressure and 520C of temperature), was used as experimental samples for typical metamorphic rocks composing oceanic crust in warm subduction zones. Constant strain rete experiments and strain rate step experiment were conducted at 1.0 GPa of confining pressure, 400 ~ 500C of temperature and 10-5 ~ 5×10-7 1/s of strain rate. At stable conditions of samples (1 GPa of confining pressure and 400 and 500C of temperature), differential stresses were higher than 1 GPa. Microstructure of recovered samples showed backing and several localized shear zones. Although

  1. Archean upper crust transition from mafic to felsic marks the onset of plate tectonics. (United States)

    Tang, Ming; Chen, Kang; Rudnick, Roberta L


    The Archean Eon witnessed the production of early continental crust, the emergence of life, and fundamental changes to the atmosphere. The nature of the first continental crust, which was the interface between the surface and deep Earth, has been obscured by the weathering, erosion, and tectonism that followed its formation. We used Ni/Co and Cr/Zn ratios in Archean terrigenous sedimentary rocks and Archean igneous/metaigneous rocks to track the bulk MgO composition of the Archean upper continental crust. This crust evolved from a highly mafic bulk composition before 3.0 billion years ago to a felsic bulk composition by 2.5 billion years ago. This compositional change was attended by a fivefold increase in the mass of the upper continental crust due to addition of granitic rocks, suggesting the onset of global plate tectonics at ~3.0 billion years ago. Copyright © 2016, American Association for the Advancement of Science.

  2. The eruptive history and magmatic evolution of Aluto volcano: new insights into silicic peralkaline volcanism in the Ethiopian rift (United States)

    Hutchison, William; Pyle, David M.; Mather, Tamsin A.; Yirgu, Gezahegn; Biggs, Juliet; Cohen, Benjamin E.; Barfod, Dan N.; Lewi, Elias


    The silicic peralkaline volcanoes of the East African Rift are some of the least studied volcanoes on Earth. Here we bring together new constraints from fieldwork, remote sensing, geochronology and geochemistry to present the first detailed account of the eruptive history of Aluto, a restless silicic volcano located in a densely populated section of the Main Ethiopian Rift. Prior to the growth of the Aluto volcanic complex (before 500 ka) the region was characterized by a significant period of fault development and mafic fissure eruptions. The earliest volcanism at Aluto built up a trachytic complex over 8 km in diameter. Aluto then underwent large-volume ignimbrite eruptions at 316 ± 19 ka and 306 ± 12 ka developing a 42 km2 collapse structure. After a hiatus of 250 ka, a phase of post-caldera volcanism initiated at 55 ± 19 ka and the most recent eruption of Aluto has a radiocarbon age of 0.40 ± 0.05 cal. ka BP. During this post-caldera phase highly-evolved peralkaline rhyolite lavas, ignimbrites and pumice fall deposits have erupted from vents across the complex. Geochemical modelling is consistent with rhyolite genesis from protracted fractionation (> 80%) of basalt that is compositionally similar to rift-related basalts found east of the complex. Based on the style and volume of recent eruptions we suggest that silicic eruptions occur at an average rate of 1 per 1000 years, and that future eruptions of Aluto will involve explosive emplacement of localised pumice cones and effusive obsidian coulees of volumes in the range 1-100 × 106 m3.

  3. Mafic dykes of the Vestfold Hills, East Antarctica. An analysis of the emplacement mechanism of tholeiitic dyke swarms and of the role of dyke emplacement during crustal extension

    NARCIS (Netherlands)

    Hoek, J.D.


    Mafic dyke swarms are common in Proterozoic continental crustal terrains. Although it is generally recognized that parallel mafic dyke swarms are formed in extensional tectonic settings and that they accommodate in the order of 10% of extensional strain, the tectonics and geodynamics of dyke

  4. Genesis of Soils Formed from Mafic Igneous Rock in the Atlantic Forest Environment

    Directory of Open Access Journals (Sweden)

    Adailde do Carmo Santos


    Full Text Available ABSTRACT Different parent materials participate in the formation of soils in the hilly landscape of “Mar de Morros” in the Atlantic Forest environment. Those derived from mafic igneous rock (gabbro frequently show erosion problems because of land use, which is aggravated by the mountainous relief and soil attributes. This study evaluated the main pedogenic processes of soils formed from mafic igneous rock (gabbro in a toposequence in Pinheiral (RJ by characterizing physical, chemical, mineralogical and micromorphological attributes. The profiles are located at different sections in the toposequence: summit (P1, shoulder (P2, backslope (P3 and footslope (P4.They were classified according to the Brazilian System of Soil Classification (SiBCS and correlated to Soil Taxonomy. The soil morphology of profiles P2, P3 and P4 is expressed by a brownish-red color, blocky structure with high to moderate development, clay films and clay loam to clay texture, with a textural B horizon. P1 shows less development, with a shallow profile and the sequence of horizons A-C-Cr. The soils have a slightly low degree of weathering, identified by the presence of pyroxenes and feldspars in the sand fraction and montorillonite in the clay fraction; the sum of bases is from 15 to 24 cmolc kg-1; and cation exchange capacity (CEC is from 12 to 22 cmolc kg-1. A significant presence of clay skins was observed in the field and was confirmed by thin section analysis, which showed features such as argillans, ferriargillans and iron nodules. The soil profile at the summit (P1 was classified as Neossolo Regolítico Órtico (Typic Udorthents, and the other profiles as Chernossolo Argilúvicos Órticos (Typic Argiudolls.

  5. Kyanite-eclogite to amphibolite fades evolution of hydrous mafic and pelitic rocks, Adula nappe, Central Alps (United States)

    Heinrich, Christoph A.


    In the southern Adula nappe (Central Alps), two stages of regional metamorphism have affected mafic and pelitic rocks. Earlier eclogite facies with a regional zonation from glaucophane eclogites to kyanite-hornblende eclogites was followed by a Tertiary overprint which varied from greenschist to high-grade amphibolite facies. Despite a common metamorphic history, contrasting equilibration conditions are often recorded by high-pressure mafic eclogite and adjacent predominantly lower-pressure pelite assemblages. This pressure contrast may be explained by different overprinting rates of the two bulk compositions during unloading. The rates are controlled by a mechanism in which dehydrating metapelites provide the H2O required for simultaneous overprinting of enclosed mafic eclogites by hydration. Quantitative mass balance modelling based on corona textures is used to show that overprinting of meta pelites during unloading involved dehydration reactions. The relatively rapid rate of dehydration reactions led to nearly complete reequilibration of metapelites to amphibolite facies assemblages. After the formation during high-pressure metamorphism of mafic eclogites, later lower-pressure reequilibration by hydration to amphibolites was slow, and therefore incomplete, because it depended on large scale transport of H2O from adjacent, dehydrating metapelites. The facies contrast observed between rocks of different bulk composition is thus a consequence of the general tendency of metamorphic rocks to retain the most dehydrated assemblage as the final recorded state.

  6. Silicate release from glass for pharmaceutical preparations. (United States)

    Bohrer, Denise; Bortoluzzi, Fabiana; Nascimento, Paulo Cícero; Carvalho, Leandro Machado; Ramirez, Adrian Gustavo


    Glass is made of polymeric silica and other minor components, which are necessary for turning the silica into a material more easily moldable and resistant to temperature changes. Glass containers for pharmaceutical usage are classified according to their resistance to a chemical attack, a test carried out in the presence of water and heat. The test is designed to show the released alkalinity, a variable dependent on the amount of sodium oxide, one of the minor components added to the glass mass. In this work, the release of silica from glass by action of constituents from pharmaceutical formulations was investigated. The study included products used in large volumes and usually stored in glass containers. Solutions of amino acids, electrolytes, glucose, oligoelements and others such as heparin and sodium bicarbonate were individually stored in glass containers and heated at 121 degrees C for 30min, as in the water attack test. The test was also carried out only with water, where the pH varied from 2 to 12. The released silicate was measured either by photometry or atomic absorption spectrometry, depending on the nature of the sample. The results showed that silicate is released during the heating cycle even if the contact is with pure water only. The pH exerts a considerable influence on the release, being that the higher the pH, the higher the silica dissolved. An elevated pH, however, is not the only factor responsible for silica dissolution. While in the solutions of NaCl, KCl, Mg Cl2 and ZnSO4 and in most of the amino acids, the concentration of silicate was as high as in pure water (0.1-1.0mg Si/L). In the solutions of sodium acetate, bicarbonate and gluconate, its concentration was much higher, over 30mg Si/L. These results were confirmed by the analysis of commercial products, where in solutions of amino acids the level of silicate ranged from 0.14 to 0.19mg Si/L. On the other hand, calcium gluconate, sodium bicarbonate and potassium phosphate presented

  7. Three Dimensional Analysis of Mafic Pumice from the 1999 sub-Plinian eruption of Shishaldin Volcano, Alaska (United States)

    Szramek, L. A.


    Fragmentation, the transition that occurs from magma with gas to gas with tephra, is thought to be recorded in vesicular pumice. This requires that the vesicularity of the pumice is frozen at the time of fragmentation. In mafic systems, this assumption is likely invalid. The kinetics of a mafic systems should allow for post-fragmentation deformation of the melt. Past studies have shown that mafic pumice from Shishaldin have crystallized post-fragmentation, increasing as much as 50%. Kinetics of crystal growth are slower than the kinetics of vesicle growth, therefore I expect a similar pattern of increase in vesicularity with distance from the rim to be found. This study examines how the vesicularity of mafic pumice varies with distance from the rim. I have excluded any vesicles that connect to the outside of each pumice. CT data has been gathered on 3 mafic pumice from the 1999 sub Plinian eruption of Shishaldin volcano. The size of each vesicle has been determined with BLOB 3D. A freeware program from the UTCT Lab. Determination of the exterior of each pumice was determined via the program Aviso. This exterior information was converted into a distance form rim gray scale distance map. This distance data, along with the size data, will be combined to determine how post-fragmentation deformation of the melt effects the growth a vesicles. I expect to find that the rims of the three pumice have similar vesicle sizes whereas the interior will have larger vesicle sizes. If this is found, it will mean that vesicle information is recording pre/during/post fragmentation information. If the rims of the vesicles are similar, then that suggests they are recording information from the time of fragmentation. This will allow a better understanding of how vesicles form in natural systems. The next phase of this project is too look at how this data is recorded in a two-dimensional sample.

  8. The genesis of Mo-Cu deposits and mafic igneous rocks in the Senj area, Alborz magmatic belt, Iran (United States)

    Nabatian, Ghasem; Li, Xian-Hua; Wan, Bo; Honarmand, Maryam


    The geochemical and isotopic investigations were provided on the Upper Eocene Senj mafic intrusion and Mo-Cu mineralization to better understand the tectono-magmatic evolution and metallogeny of the central part of the Alborz magmatic belt. The Senj mafic intrusion is composed of gabbro to monzodiorite and monzonite in lithology, and intruded as a sill into volcano-sedimentary rocks of the Eocene Karaj Formation. The Karaj Formation consists of volcano-sedimentary rocks, such as altered crystalline to shaly tuffs. The Senj intrusion (39.7 ± 0.4 Ma) shows LILE and LREE enrichment and negative anomaly of Nb, Ta and Ti, the geochemical signatures similar to those from subduction-related mafic magmas. The Hf-O zircon analyses yield ɛHf(t) values of + 4.1 to + 11.1 and δ18O values of + 4.8 to + 6.2‰. The zircon isotopic signatures together with shoshonitic affinity in the Senj mafic samples suggest partial melting of an enriched lithospheric mantle that had already been metasomatized by slab-derived melts and fluids. The Mo-Cu mineralization mainly occurs as veins and veinlets in the volcano-sedimentary rocks of the Karaj Formation and is dominated by molybdenite with minor amounts of chalcopyrite, bornite, pyrite and tetrahedrite-tennantite. The associated gangue minerals are tremolite, actinolite, quartz, calcite, chlorite and epidote. The Senj Mo-Cu deposit formed in volcano-sedimentary rocks following the emplacement of the Late Eocene Senj sill. The source of molybdenite in the Senj deposit is dominantly from crustal materials as it is revealed by Re contents in the molybdenite minerals (0.5 to 0.7 ppm). In fact, the molybdenite occurrence may be a remobilization process related to the emplacement of the Senj mafic magma.

  9. Mechanical Anisotropies and Mechanisms of Mafic Magma Ascent in Middle Continental Crust: The Sondalo Gabbroic Complex (N Italy) (United States)

    Petri, B.; Mohn, G.; Skrzypek, E.; Mateeva, T.; Robion, P.; Schulmann, K.; Manatschal, G.; Müntener, O.


    The ascent mechanisms of magma through the continental crust remain a long standing controversy. The pathways of intermediate to felsic magmas can be continuously traced through the crust, however mafic magma transfer between lower and upper crustal levels is rarely documented. To fill this gap, we explore the mechanisms of mafic magma ascent and emplacement in middle continental crust. We characterize the structure and anisotropy of magnetic susceptibility (AMS) fabrics of a mid-crustal mafic complex (Sondalo gabbroic complex, N-Italy) together with Anisotropy of Anhysteretic Remanent Magnetization (AARM) and Crystallographic Preferred Orientation (CPO) data. Field data indicate concentric gabbroic to dioritic intrusions emplaced in sub-vertically foliated metasedimentary host-rocks. The petrofabrics and magnetic fabrics of the pluton (foliations and lineations) are coaxial, syn-magmatic and sub-vertical. U-Pb dating of zircons along with the structural record of the plutonic rocks indicate two major pulses of magma emplacement in sub-vertical channels. (1) The concordant orientation between the magmatic foliation and the host-rock xenoliths in the center of the pluton suggest that the early emplacement phase occurred through magma fracture opening subparallel to the vertical fabric of the host rocks at 289-288 Ma. (2) The second magma ascent phase was controlled by a change in the rheology of the host-rock and the mafic magma. The temperature increase in the contact aureole induced partial melting and decreased its mechanical strength, whereas the viscosity of the mafic magma increased due to progressive cooling and crystallization. This caused an en-masse rise of the crystal mush and drag forces resulting in the formation of a vertical foliation in the metamorphic aureole and a weaker but concordant magmatic foliation at the rim of the pluton. This ascent phase is slightly younger (288-285 Ma) and accounts for the contrasted P-T evolution recorded by

  10. Phreatomagmatic explosive eruptions along fissures on the top of mafic stratovolcanoes with overlapping compound calderas (United States)

    Nemeth, Karoly; Geshi, Nobuo


    On near summit flank eruptions on stratovolcanoes it is commonly inferred that external water to have little or no influence on the course of the eruptions. Hence eruptions are typicaly "dry" that form spatter-dominated fissures and scoria cones. This assumption is based on that in elevated regions - especially on steep slopes - the hydrogeological conditions are not favourable to store large volume of ground water that can have effect on the eruptions. However there is some controversial trend of eruption progression from an early dry eruption below the summit that later turn to be phreatomagmatic as the eruption locus migrates toward the summit. The Suoana Ccrater on top of Miyakejima Island's mafic stratovolcano is a fine example to demonstrate such process. Suona Crater is the topmost crater of the 3 km long fissure aligned chain of small-volume volcanoes that formed in the 7th century flank of the summit region of the Miyakejima mafic stratovolcano. The oval shape crater of Suona (400 x 300 m) is surrounded by a tuff ring that developed over lava flows and epiclastic deposits accumulated in an older caldera forming about a tuff ring that is about 25 m in its thickest section with a basal consistent lava spatter dominated unit gradually transforming into a more scoria-dominated middle unit. A caldera-forming eruption in AD 2000 half-sectioned the Suona Crater exposing of its internal diatreme - crater in-fill - tephra rim succession providing a unique opportunity to understand the 3D architecture of the volcano. Toward the top of the preserved and exposed tuff ring section a clear gradual transition can be seen toward more abundance of chilled dark juvenile particles providing a matrix of a coarse ash that commonly hold cauliflower lapilli and bomb. This transition indicates that the eruption progressed from an early dry explosive phase such as lava fountaining to be a more Strombolian style explosive eruption that later on turned to be heavily influenced by

  11. Mantle-derived sources of syenites from the A-type igneous suites - New approach to the provenance of alkaline silicic magmas (United States)

    Litvinovsky, B. A.; Jahn, B. M.; Eyal, M.


    Granite is generally dominant in A-type igneous suites but these frequently include also alkali feldspar- and peralkaline- syenite and quartz syenite. Such syenites can provide essential information about magma sources and mode of generation of A-type silicic magma. This paper addresses the petrogenesis of syenites based on comparisons between the Mongolian-Transbaikalian Belt, Russia (MTB), and the northern Arabian-Nubian Shield (ANS) as exposed in the Sinai Peninsula, Egypt and adjacent areas of southern Israel. The syenitic rocks from MTB and ANS are characterized by high alkali content (Na2O + K2O = 10.5 to 12.5 wt.%) and are assigned to alkaline metaluminous and peralkaline granitoids. Peralkaline syenites are generally richer in Na and contain slightly less K and Ba than are metaluminous granitoids. REE abundances are similar in all types of syenites. The Eu/Eu* ratios range commonly from 0.35 to 0.65, although higher values, up to 1.15, attributed to presence of accumulated Afs and minor Pl, also occur in some plutons. The geochemical and Sr-Nd isotope characteristics of associated syenite, granite and monzogabbro from five igneous suites ( 80 samples) suggest that the main rock types, silicic and mafic, are cogenetic in each suite. Syenite magmas were produced from mantle-derived source with little, if any silicic crustal component. The generation of abundant A-type granite and syenite magmas in the young juvenile crust (ANS) argues that old continental crust is not required for generation of highly alkaline silicic magmas, as commonly advocated. The most probable source of both syenite and granite was mantle-derived K-rich shoshonitic monzogabbro. The bimodal character of the A-type suites suggests that partial melting of monzogabbro, rather than fractional crystallization of basic magma, accompanied with enrichment of a cumulate phase in the mafic units, was the dominant mode of granitoid magma formation. Granite magmas were produced in the lower crust at


    Directory of Open Access Journals (Sweden)

    Nediljka Gaurina-Međimurec


    Full Text Available The silicate-based drilling fluid is a low solids KCl/polymer system with the addition of soluble sodium or potassium silicate to enhance inhibition and wellbore stability. Silicate-based drilling fluids exhibit remarkable shale and chalk stabilizing properties, resulting in gauge hole and the formation of firm cuttings when drilling reactive shales and soft chalks. Silicates protect shales by in-situ gellation when exposed to the neutral pore fluid and precipitation, which occurs on contact with divalent ions present at the surface of the shale. Also, silicates prevent the dispersion and washouts when drilling soft chalk by reacting with the Ca2+ ions present on chalk surfaces of cutting and wellbore to form a protective film. The silicate-based drilling fluid can be used during drilling hole section through shale interbeded anhydrite formations because of its superior shale stabilizing characteristics. However, drilling through the anhydrite can decrease the silicate concentration and change rheological and filtration fluid properties. So, the critical concentration of calcium ions should be investigated by lab tests. This paper details the mechanism of shale inhibition using silicate-based drilling fluid, and presents results of lab tests conducted to ascertain the effect of Ca2+ ions on silicate level in the fluid and the fluid properties.

  13. Determination of chlorine in silicate rocks (United States)

    Peck, L.C.


    In a rapid accurate method for the determination of chlorine in silicate rocks, the rock powder is sintered with a sodium carbonate flux containing zinc oxide and magnesium carbonate. The sinter cake is leached with water, the resulting solution is filtered, and the filtrate is acidified with nitric acid. Chlorine is determined by titrating this solution with mercuric nitrate solution using sodium nitroprusside as the indicator. The titration is made in the dark with a beam of light shining through the solution. The end point of the titration is found by visually comparing the intensity of this beam of light with that of a similar beam of light in a reference solution.

  14. Microbial dissolution of silicate materials. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Schwartzman, D. [Howard Univ., Washington, DC (United States). Dept. of Biology


    The objective of this research was to better understand the role of selected thermophilic bacteria in the colonization and dissolution of silicate minerals, with potential applications to the HDR Project. The demonstration of enhanced dissolution from microbial effects is critically dependent on providing a mineral bait within a media deficient in the critical nutrient found in the mineral (e.g., Fe). Reproducible experimental conditions in batch experiments require agitation to expose mineral powders, as well as nearly similar initial conditions for both inoculated cultures and controls. It is difficult, but not impossible to ensure reproducible conditions with microbes favoring filamentous growth habits.

  15. Geochemistry and petrogenesis of proterozoic mafic dykes in north Kerala, southwestern Indian Shield - Preliminary results (United States)

    Radhakrishna, T.; Gopakumar, K.; Murali, A. V.; Mitchell, J. G.


    Mafic dyke intrusions occur in three distinct orientations ( NNW-SSE and NW-SE and NE-SW) in north Kerala regions, the southwestern part of the Indian Shield. Dating of two NNW-SSE trending dykes by K-Ar method has yielded Middle Proterozoic ages (ca. 1660 Ma and ca. 1420 Ma respectively). Our initial geochemical results on these dyke rocks (0.65-0.15 wt pct K2O, 0.37-0.38 wt pct P2O5, 3.30-1.00 wt pct TiO2, 11-1 p.p.m. Rb, 250-90 p.p.m. Sr, 230-40 p.p.m. Ba, 160-40 p.p.m. Zr, and 30-10 x chondrite rare earth elemental abundances) indicate a transitional character between abyssal and plateau tholeiites. Petrogenetic modelling suggests that the dyke compositions have been derived by different degrees of partial melting of a heterogenous source mantle. The mantle sources with accessory amphibole and/or garnet, variably enriched in LREE and LIL elements, are compatible with the observed geochemical data.

  16. Thermochemistry of dense hydrous magnesium silicates (United States)

    Bose, Kunal; Burnley, Pamela; Navrotsky, Alexandra


    Recent experimental investigations under mantle conditions have identified a suite of dense hydrous magnesium silicate (DHMS) phases that could be conduits to transport water to at least the 660 km discontinuity via mature, relatively cold, subducting slabs. Water released from successive dehydration of these phases during subduction could be responsible for deep focus earthquakes, mantle metasomatism and a host of other physico-chemical processes central to our understanding of the earth's deep interior. In order to construct a thermodynamic data base that can delineate and predict the stability ranges for DHMS phases, reliable thermochemical and thermophysical data are required. One of the major obstacles in calorimetric studies of phases synthesized under high pressure conditions has been limitation due to the small (less than 5 mg) sample mass. Our refinement of calorimeter techniques now allow precise determination of enthalpies of solution of less than 5 mg samples of hydrous magnesium silicates. For example, high temperature solution calorimetry of natural talc (Mg(0.99) Fe(0.01)Si4O10(OH)2), periclase (MgO) and quartz (SiO2) yield enthalpies of drop solution at 1044 K to be 592.2 (2.2), 52.01 (0.12) and 45.76 (0.4) kJ/mol respectively. The corresponding enthalpy of formation from oxides at 298 K for talc is minus 5908.2 kJ/mol agreeing within 0.1 percent to literature values.

  17. Carbon Mineralization Using Phosphate and Silicate Ions (United States)

    Gokturk, H.


    Carbon dioxide (CO2) reduction from combustion of fossil fuels has become an urgent concern for the society due to marked increase in weather related natural disasters and other negative consequences of global warming. CO2 is a highly stable molecule which does not readily interact with other neutral molecules. However it is more responsive to ions due to charge versus quadrupole interaction [1-2]. Ions can be created by dissolving a salt in water and then aerosolizing the solution. This approach gives CO2 molecules a chance to interact with the hydrated salt ions over the large surface area of the aerosol. Ion containing aerosols exist in nature, an example being sea spray particles generated by breaking waves. Such particles contain singly and doubly charged salt ions including Na+, Cl-, Mg++ and SO4--. Depending on the proximity of CO2 to the ion, interaction energy can be significantly higher than the thermal energy of the aerosol. For example, an interaction energy of 0.6 eV is obtained with the sulfate (SO4--) ion when CO2 is the nearest neighbor [2]. In this research interaction between CO2 and ions which carry higher charges are investigated. The molecules selected for the study are triply charged phosphate (PO4---) ions and quadruply charged silicate (SiO4----) ions. Examples of salts which contain such molecules are potassium phosphate (K3PO4) and sodium orthosilicate (Na4SiO4). The research has been carried out with first principle quantum mechanical calculations using the Density Functional Theory method with B3LYP functional and Pople type basis sets augmented with polarization and diffuse functions. Atomic models consist of the selected ions surrounded by water and CO2 molecules. Similar to the results obtained with singly and doubly charged ions [1-2], phosphate and silicate ions attract CO2 molecules. Energy of interaction between the ion and CO2 is 1.6 eV for the phosphate ion and 3.3 eV for the silicate ion. Hence one can expect that the selected

  18. Experimental constraints on silicic magma storage at Hekla volcano (Iceland) and potential implications for pre-eruptive deformation (United States)

    Weber, Gregor; Castro, Jonathan


    Understanding the conditions that culminate in explosive eruptions of silicic magma is important for volcanic hazards mitigation. However, geological records of volcanoes typically show a wide range of eruptive behaviour and magnitude for individual eruptive centres. In order to evaluate future scenarios of eruption precursors, namely pre-eruptive deformation, magmatic system variables for different eruption types need to be constrained. Here we use experimental petrology and microanalysis of plagioclase crystals to clarify the P-T-x state under which rhyodacitic melts accumulated prior to Hekla Volcano's H3 eruption; the largest Holocene Plinian eruption in Iceland. Cobalt-buffered, H2O-saturated phase equilibrium experiments reproduce the natural H3 pumice phenocryst assemblage (pl>fa+cpx>ilm+mt>ap+zrc) and glass chemistry, at 850±15˚C and PH2O of 130 to 175 MPa, implying shallow crustal magma storage between 5 and 6.6 km. The systematics of FeO and anorthite (CaAl2Si2O8) content in plagioclase reveal that thermal gradients were more important than compositional mixing or mingling within this magma reservoir. As these findings indicate magma storage much shallower than is currently thought of Hekla's mafic system, we use the constrained storage depth combined with deformation modelling to help forecast surface uplift patterns that could stem from the input of magma in reservoirs at different depth prior to an eruption. Using finite element modelling, we show that the vertical surface displacements for silicic magma accumulation sourced from about 6 km depths could potentially be more focussed than those observed in recent mafic events, which are fed from a lower crustal storage zone. Our results show how petrological reconstruction of magmatic system variables can link signs of pre-eruptive geophysical unrest to magmatic processes occurring in reservoirs at shallow depths. This will enhance our abilities to use deformation measurements (e.g. InSAR and GPS) in

  19. Clinopyroxene trace element compositions of cumulate mafic rocks and basalts from the Hercynian Moroccan Central Meseta: Petrogenetic implications (United States)

    Driouch, Y.; Béziat, D.; Grégoire, M.; Laguenini, F.; Abbou, M. Ben; Ntarmouchant, A.; Roddaz, M.; Dahire, M.; Bennouna, A.; Belkasmi, M.; Brusset, S.; Debat, P.


    In the Fourhal foreland basin, in the north-eastern part of the Marrocan Central Meseta, mafic series are represented by basalts interbedded with Early Namurian turbidites and by numerous mafic sills, including the Marziqallal sill detailed here. The study of the trace element compositions of the clinopyroxenes, a ubiquitous mineral in the gabbroic sill and basalts, indicate that these two formations are derived from a similar parental magma. This magma evolved following a general fractional crystallization process involving the cumulation of clinopyroxene, then of ilmenite, occurring within the sill and having a leading role in the composition of the associated basalts. Calculated parental melts inferred from clinopyroxene analyses from the various cumulative units of the sill have trace element patterns similar to the one found for the basaltic flows. These patterns are compatible with magma and clinopyroxene compositions from a subduction-related geotectonic setting.

  20. Late Cretaceous intraplate silicic volcanism in the Lake Chad region: incipient continental rift volcanism vs. Cameroon Line volcanism (United States)

    Shellnutt, G.; Lee, T. Y.; Torng, P. K.; Yang, C. C.


    The crustal evolution of west-central Africa during the Cretaceous was directly related to plate motion associated with the opening of the central Atlantic Ocean. Late Cretaceous (~66 Ma) to recent magmatism related to the Cameroon Line stretches from Northern Cameroon (i.e. Golda Zuelva) to the Gulf of Guinea (i.e. Pagalu) and is considered to be due to mantle-crust interaction. The volcanic rocks at Hadjer el Khamis, west-central Chad, are considered to be amongst the oldest volcanic rocks of the Cameroon Line but their relationship is uncertain because they erupted during a period of a regional extension associated with the opening of the Late Cretaceous (~75 Ma) Termit basin. The silicic volcanic rocks can be divided into a peraluminous group and a peralkaline group with both rock types having similar chemical characteristics as within-plate granitoids. In situ U/Pb zircon dating yielded a mean 206Pb/238U age of 74.4 ± 1.3 Ma and indicates the rocks erupted ~10 million years before the next oldest eruption attributed to the Cameroon Line. The Sr isotopes (i.e. ISr = 0.7050 to 0.7143) show a wide range but the Nd isotopes (i.e. 143Nd/144Ndi = 0.51268 to 0.51271) are more uniform and indicate that the rocks were derived from a moderately depleted mantle source. Major and trace elemental modeling show that the silicic rocks likely formed by shallow fractionation of a mafic parental magma where the peraluminous rocks experienced crustal contamination and the peralkaline rocks did not. The silicic rocks are more isotopically similar to Late Cretaceous basalts in the Doba and Bongor basins (i.e. ISr = 0.7040 to 0.7060; 143Nd/144Ndi = 0.51267 to 0.51277) of southern Chad than to rocks of the Cameroon Line (i.e. ISr = 0.7026 to 0.7038; 143Nd/144Ndi = 0.51270 to 0.51300). Given the age and isotopic compositions, it is likely that the silicic volcanic rocks of the Lake Chad area are related to Late Cretaceous extensional tectonics rather than to Cameroon Line magmatism.

  1. Fluid Inclusion Study of Quartz Xenocrysts in Mafic Dykes from Kawant Area, Chhota Udaipur District, Gujarat, India


    Randive Kirtikumar; Hurai Vratislav


    Unusual mafic dykes occur in the proximity of the Ambadongar Carbonatite Complex, Lower Narmada Valley, Gujarat, India. The dykes contain dense population of quartz xenocrysts within the basaltic matrix metasomatised by carbonate-rich fluids. Plagioclase feldspars, relict pyroxenes, chlorite, barite, rutile, magnetite, Fe-Ti oxides and glass were identified in the basaltic matrix. Quartz xenocrysts occur in various shapes and sizes and form an intricate growth pattern with carbonates. The xen...

  2. 2480 Ma mafic magmatism in the northern Black Hills, South Dakota: A new link connecting the Wyoming and Superior cratons (United States)

    Dahl, P.S.; Hamilton, M.A.; Wooden, J.L.; Foland, K.A.; Frei, R.; McCombs, J.A.; Holm, D.K.


    The Laramide Black Hills uplift of southwest South Dakota exposes a Precambrian crystalline core of ???2560-2600 Ma basement granitoids nonconformably overlain by two Paleoproterozoic intracratonic rift successions. In the northern Black Hills, a 1 km thick, layered sill (the Blue Draw metagabbro) that intrudes the older rift succession provides a key constraint on the timing of mafic magmatism and of older rift-basin sedimentation. Ion microprobe spot analyses of megacrysts of magmatic titanite from a horizon of dioritic pegmatite in the uppermost sill portion yield a 207Pb/206Pb upper-intercept age of 2480 ?? 6 Ma (all age errors ??2??), comparable to two-point 207Pb/206Pb errorchron ages obtained by Pb stepwise leaching of the same titanites. Nearly concordant domains in coexisting magmatic zircon yield apparent spot ages ranging from 2458 ?? 16 to 2284 ?? 20 Ma (i.e., differentially reset along U-Pb concordia), and hornblende from an associated metadiorite yields a partially reset date with oldest apparent-age increments ranging between 2076 ?? 16 and 2010 ?? 8 Ma. We interpret these data as indicating that an episode of gabbroic magmatism occurred at 2480 Ma, in response to earlier rifting of the eastern edge of the Wyoming craton. Layered mafic intrusions of similar thickness and identical age occur along a rifted belt in the southern Superior craton (Sudbury region, Ontario). Moreover, these mafic intrusions are spatially aligned using previous supercontinent restorations of the Wyoming and Superior cratons (Kenorland-Superia configurations). This new "piercing point" augments one previously inferred by spatial-temporal correlation of the Paleoproterozoic Huronian (southern Ontario) and Snowy Pass (southeastern Wyoming) supergroups. We propose that layered mafic intrusions extending from Nemo, South Dakota, to Sudbury, Ontario, delineate an axial rift zone along which Wyoming began to separate from Superior during initial fragmentation of the Neoarchean

  3. Suture Dynamics of the Banda Arc Collision Zone: Geochemical and Age Analysis of Ultramafic and Mafic Bodies in Timor, Indonesia (United States)

    Valenza, J. M.; Harris, R. A.; Spencer, C. J.; Hoiland, C. W.; Flores, J. A.


    New age and geochemical data confirm that most ultramafic bodies on the north coast of Timor are derived from the distal reaches of the Australian continental margin lower plate that was exhumed by extension during Late Paleozoic to Mesozoic rifting. The ultramafic bodies were accreted to Timor during Late Miocene to present arc-continent collision. One of the lherzolitic ultramafic bodies near Caicua was previously unknown, but yields clear isotopic indicators that it is kin to the Hili Manu mafic and ultramafic complex further to the west. Zircon grains from metagabbro of the Hili Manu complex have cores with mostly Early Permian ages and rims of Latest Miocene ages. Isotopic analysis indicates abyssal plain, or passive margin affinity of the Caicua ultramafic body. One important exception to this pattern are mafic and ultramafic bodies associated with the Ocussi volcanics, which yield Miocene and Pliocene ages and supra-subduction zone chemical signatures. The Ocussi body is clearly part of the upper plate of the collision and formed after collision initiated further to the east. It is also structurally higher than the Hili Manu complex and has no affinities with the Australian plate. This study documents that both the upper and lower plates of the active arc-continent collision contribute mafic and ultramafic rocks to the evolving suture zone between the Indo-Australian and Asian plates in the Banda Arc region.

  4. Petrology and Geochemistry of Calc-Silicate Schists and Calc ...

    African Journals Online (AJOL)

    Chemically the calc-silicate schists are characterized by relatively high CaO, MgO, Cr, Ni, Sr, La, Ce and Nd contents compared with the mica schist regionally associated with the marble as well as the Post-Archean Australian Shale (PAAS). Relative to the ultramafic schist the calc-silicate schists are characterized by higher ...

  5. 40 CFR 721.9513 - Modified magnesium silicate polymer (generic). (United States)


    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Modified magnesium silicate polymer (generic). 721.9513 Section 721.9513 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.9513 Modified magnesium silicate polymer (generic). (a) Chemical...

  6. [Adsorption characteristic and form distribution of silicate in lakes sediments]. (United States)

    Lü, Chang-Wei; Cui, Meng; Gao, Ji-Mei; Zhang, Xi-Yan; Wan, Li-Li; He, Jiang; Meng, Ting-Ting; Bai, Fan; Yang, Xu


    Taking surface sediments from the Wuliangsuhai Lake and Daihai Lake as adsorbent, the isothermal adsorption experiments of silicate on sediments were carried out and the adsorption behavior was explained by Langmuir, Freundlich and Temkin crossover-type equations, then the form distribution characters of silicate were studied after adsorption in this work. The results showed that the adsorption behavior of silicate on the two lakes sediments can be linear fitting in the lower concentration dose (Temkin crossover-type equations can be used to explain the adsorption behavior of silicate on the two lakes sediments, and the native adsorption silicate (NAS) and equilibrium silicate concentration (ESC(0)) calculated by the three equations could be used to explain the sink and source effects of the sediments from the two lakes; the silicate form distribution in the sediments after adsorption indicated that silicate adsorbed on particles were mainly added on the form of IEF-Si, CF-Si, IMOF-Si and OSF-Si, and the IMOF-Si and OSF-Si had important potential bioavailability.

  7. Fire Resistance of Wood Impregnated with Soluble Alkaline Silicates


    Andrea Marisa Pereyra; Carlos Alberto Giudice


    The aim of this paper is to determine the fire performance of wood panels (Araucaria angustifolia) impregnated with soluble alkaline silicates. Commercial silicates based on sodium and potassium with 2.5/1.0 and 3.0/1.0 silica/alkali molar ratios were selected; solutions and glasses ...

  8. Natural Weathering Rates of Silicate Minerals (United States)

    White, A. F.


    Silicates constitute more than 90% of the rocks exposed at Earth's land surface (Garrels and Mackenzie, 1971). Most primary minerals comprising these rocks are thermodynamically unstable at surface pressure/temperature conditions and are therefore susceptible to chemical weathering. Such weathering has long been of interest in the natural sciences. Hartt (1853) correctly attributed chemical weathering to "the efficacy of water containing carbonic acid in promoting the decomposition of igneous rocks." Antecedent to the recent interest in the role of vegetation on chemical weathering, Belt (1874) observed that the most intense weathering of rocks in tropical Nicaragua was confined to forested regions. He attributed this effect to "the percolation through rocks of rain water charged with a little acid from decomposing vegetation." Chamberlin (1899) proposed that the enhanced rates of chemical weathering associated with major mountain building episodes in Earth's history resulted in a drawdown of atmospheric CO2 that led to periods of global cooling. Many of the major characteristics of chemical weathering had been described when Merrill (1906) published the groundbreaking volume Rocks, Rock Weathering, and Soils.The major advances since that time, particularly during the last several decades, have centered on understanding the fundamental chemical, hydrologic, and biologic processes that control weathering and in establishing quantitative weathering rates. This research has been driven by the importance of chemical weathering to a number environmentally and economically important issues. Undoubtedly, the most significant aspect of chemical weathering is the breakdown of rocks to form soils, a process that makes life possible on the surface of the Earth. The availability of many soil macronutrients such as magnesium, calcium, potassium, and PO4 is directly related to the rate at which primary minerals weather. Often such nutrient balances are upset by anthropogenic

  9. Southern continuation of the Wakeham Group and Robe-Noire mafic suite (eastern Grenville Province) from hydrocarbon-targeted seismic reflection data on Anticosti Island, Quebec, Canada1

    National Research Council Canada - National Science Library

    Pinet, Nicolas


    .... The reflective seismic unit likely corresponds to the southern extension of the Mesoproterozoic Wakeham Group and Robe-Noire mafic sills that are exposed on the nearby north shore of the Gulf of St...

  10. The Rice High-Affinity K+ Transporter OsHKT2;4 Mediates Mg2+ Homeostasis under High-Mg2+ Conditions in Transgenic Arabidopsis

    Directory of Open Access Journals (Sweden)

    Chi Zhang


    Full Text Available Rice (Oryza sativa; background Nipponbare contains nine HKT (high-affinity K+ transport-like genes encoding membrane proteins belonging to the superfamily of Ktr/TRK/HKT. OsHKTs have been proposed to include four selectivity filter-pore-forming domains homologous to the bacterial K+ channel KcsA, and are separated into OsHKT1s with Na+-selective activity and OsHKT2s with Na+-K+ symport activity. As a member of the OsHKT2 subfamily, OsHKT2;4 renders Mg2+ and Ca2+ permeability for yeast cells and Xenopus laevis oocytes, besides K+ and Na+. However, physiological functions related to Mg2+in planta have not yet been identified. Here we report that OsHKT2;4 from rice (O. sativa; background Nipponbare functions as a low-affinity Mg2+ transporter to mediate Mg2+ homeostasis in plants under high-Mg2+ environments. Using the functional complementation assay in Mg2+-uptake deficient Salmonella typhimurium strains MM281 and electrophysiological analysis in X. laevis oocytes, we found that OsHKT2;4 could rescue the growth of MM281 in Mg2+-deficient conditions and induced the Mg2+ currents in oocytes at millimolar range of Mg2+. Additionally, overexpression of OsHKT2;4 to Arabidopsis mutant lines with a knockout of AtMGT6, a gene encoding the transporter protein necessary for Mg2+ adaptation in Arabidopsis, caused the Mg2+ toxicity to the leaves under the high-Mg2+ stress, but not under low-Mg2+ environments. Moreover, this Mg2+ toxicity symptom resulted from the excessive Mg2+ translocation from roots to shoots, and was relieved by the increase in supplemental Ca2+. Together, our results demonstrated that OsHKT2;4 is a low-affinity Mg2+ transporter responsible for Mg2+ transport to aerials in plants under high-Mg2+ conditions.

  11. Paleomagnetism of Proterozoic mafic dikes from the Tobacco Root Mountains, southwest Montana (United States)

    Harlan, S.S.; Geissman, J. Wm; Snee, L.W.


    Paleomagnetic data from Proterozoic mafic dikes in southwestern Montana provides evidence for two distinct episodes of subparallel dike emplacement at ca. 1450 and 780 Ma. Published geochemical data from dikes in the southern Tobacco Root Mountains has identified three distinct compositional groups, termed groups A, B, and C. Geochronological data from the group A dikes yielded a Sm-Nd age of 1448 ?? 49 Ma. Emplacement of these dikes is thought to reflect mafic magmatism associated with extension accompanying development of the adjacent Mesoproterozoic Belt Basin. Paleomagnetic results from these dikes and a group C dike yield antipodal magnetizations with a group-mean direction of D = 225.0??, I = 61.8?? (k = 27.9, ??95 = 7.7??, N = 14 independent means/24 sites). The average paleomagnetic pole (8.7??N, 216.1??E, A95 = 10.3??) is considered to be primary on the basis of positive baked contact tests and similarity to poles of ca. 1.45-1.4 Ga from intrusions elsewhere in North America, but is discordant with respect to poles from age equivalent sedimentary rocks of the Meosoproterozoic Belt Supergroup. 40Ar/39Ar dates from geochemical group B dikes are consistent with published U-Pb dates that demonstrate dike emplacement at 780 Ma as part of the regional Gunbarrel magmatic event. Hornblende concentrates from the group B dikes yield 40Ar/39Ar apparent ages of 778-772 Ma, whereas biotite from a baked contact zone yielded a plateau date of 788 Ma. Paleomagnetic results from the group B dikes yield a mean direction of D = 301.5??, I = -17.1?? (k = 65.7, ??95 = 4.0??, N = 12 independent means/23 sites) with a paleomagnetic pole at 14.6??N, 127.0??E (A95 = 3.2??). The combination of geochronologic data, results of a baked contact test, and spatial agreement of the paleomagnetic poles with poles of similar age elsewhere in North America indicates that this is also a primary magnetization associated with dike emplacement. Paleomagnetic data from some of the Tobacco Root

  12. Diffusion controlled corona growth in mafic dykes from Southern Granulite Terrain, India and their petrological implications (United States)

    Banerjee, Ayoti; Banerjee, Meenakshi; Dutta, Upama; Sengupta, Pulak; Bhui, Uttam K.; Rajagopal, Anand; Mukhopadhyay, Dhruba


    Diffusion controlled corona growth in mafic dykes from Southern Granulite Terrain, India and their petrological implications Metamorphosed garnetiferous mafic dykes from Southern Granulite Terrain (SGT) are found intruding the high grade Archaean-Palaeoproterozoic felsic orthogneiss and their retrogressed equivalent. They contain phenocrysts of clinopyroxene (Cpx) and plagioclase (Pl) that preserve ophitic, subophitic and intergranular textures. The clinopyroxene contains closely spaced cleavage-parallel exsolution lamellae of orthopyroxene (Opx) and tiny rods of Fe-Ti oxides. Orthopyroxene is also found around clinopyroxene as granular exsolution. Large grains of Fe-Ti oxides occur within the interstitial space. Garnet (Grt) and quartz (Qtz) form at the contact of plagioclase and clinopyroxene. The product minerals are found as symplectite and/or corona rimming the reactants. In the corona, quartz always occurs near clinopyroxene whereas garnet forms close to the plagioclase. The proportions of garnet and quartz in symplectite are fairly constant and range from 75:25 to 70:30 (vol %). Similar coronitic texture is exhibited by amphibole (Amp) and quartz. Thin amphibole+quartz corona forms between plagioclase and clinopyroxene where amphibole occurs near plagioclase and quartz near clinopyroxene, though the rock is dominated by garnet over amphibole in the corona. Corona of garnet/amphibole is also found on Fe-Ti oxides at the contact of plagioclase and the products show TiO2 enrichement when they occur near Fe-Ti oxides. Formation of hydrous amphibole from anhydrous minerals necessitates the system to be open to H2O. Additionally, balanced chemical reactions for Pl+Cpx=Grt+Qtz and Pl+Cpx=Amp+Qtz require Fe+2 incorporation to explain the observed volume proportion of the product minerals. Formation of garnet/amphibole near plagioclase and quartz near clinopyroxene indicate restricted mobility of Al and Si within the reaction domain. Preferential enrichment of TiO2

  13. Kinetics of iron oxidation in silicate melts

    Energy Technology Data Exchange (ETDEWEB)

    Magnien, V.; Neuville, D.R.; Cormier, L.; Mysen, B.O.; Pinet, O.; Richet, P


    High-temperature XANES experiments at the Fe K-edge have been used to study the kinetics of iron oxidation in a supercooled melt of Fe-bearing pyroxene composition. These experiments, made just above the glass transition between 600 and 700 deg C, show that variations in relative abundances of ferric and ferrous iron can be determined in situ at such temperatures. The kinetics of iron oxidation do not vary much with temperature down to the glass transition. This suggests that rate-limiting factor in this process is not oxygen diffusion, which is coupled to relaxation of the silicate network, but diffusion of network modifying cations along with a counter flux of electrons. To give a firmer basis to redox determinations made from XANES spectroscopy, the redox state of a series of a samples was first determined from wet chemical, Moessbauer spectroscopy and electron microprobe analyses. (authors)

  14. Selective silicate-directed motility in diatoms

    DEFF Research Database (Denmark)

    Bondoc, Karen Grace V.; Heuschele, Jan; Gillard, Jeroen


    Diatoms are highly abundant unicellular algae that often dominate pelagic as well as benthic primary production in the oceans and inland waters. Being strictly dependent on silica to build their biomineralized cell walls, marine diatoms precipitate 240 × 10(12) mol Si per year, which makes them...... the major sink in the global Si cycle. Dissolved silicic acid (dSi) availability frequently limits diatom productivity and influences species composition of communities. We show that benthic diatoms selectively perceive and behaviourally react to gradients of dSi. Cell speed increases under d......Si-limited conditions in a chemokinetic response and, if gradients of this resource are present, increased directionality of cell movement promotes chemotaxis. The ability to exploit local and short-lived dSi hotspots using a specific search behaviour likely contributes to micro-scale patch dynamics in biofilm...

  15. Thermal Ablation Modeling for Silicate Materials (United States)

    Chen, Yih-Kanq


    A general thermal ablation model for silicates is proposed. The model includes the mass losses through the balance between evaporation and condensation, and through the moving molten layer driven by surface shear force and pressure gradient. This model can be applied in the ablation simulation of the meteoroid and the glassy ablator for spacecraft Thermal Protection Systems. Time-dependent axisymmetric computations are performed by coupling the fluid dynamics code, Data-Parallel Line Relaxation program, with the material response code, Two-dimensional Implicit Thermal Ablation simulation program, to predict the mass lost rates and shape change. The predicted mass loss rates will be compared with available data for model validation, and parametric studies will also be performed for meteoroid earth entry conditions.

  16. Lithium alumino-silicate ion source development (United States)

    Roy, Prabir Kumar; Seidl, Peter A.; Kwan, Joe W.; Greenway, Wayne G.; Waldron, William L.; Wu, James K.; Mazaheri, Kavous


    We report experimental progress on Li+ source development in preparation for warm dense matter heating experiments. To uniformly heat targets to electron-volt temperatures for the study of warm dense matter, we are pursuing the use of a low (E spodumene and β-eucryptite, each of area 0.31 cm2, have been fabricated for ion emission measurements. These surface ionization sources are heated to 1200 to 1300 C where they preferentially emit singly ionized alkali ions. Tight process controls were necessary in preparing and sintering the alumino-silicate to the porous tungsten substrate to produce an emitter that gives uniform ion emission, sufficient current density and low beam emittance. Current density limit of the two kinds have been measured, and ion species identification of possible contaminants has been verified with a Wien (E x B) filter.

  17. Oceanic mafic magmatism in the Siletz terrane, NW North America: Fragments of an Eocene oceanic plateau? (United States)

    Phillips, Bethan A.; Kerr, Andrew C.; Mullen, Emily K.; Weis, Dominique


    The Siletz terrane, a predominantly mafic accreted oceanic terrane, is located in the Cascadia forearc region of Oregon, Washington and Vancouver Island. The terrane represents a late Palaeocene-Eocene large igneous province that consists of pillow lavas, massive flows and intrusive sheets. Previously it has been proposed that the Siletz terrane represents either an accreted oceanic plateau, hotspot island chain, backarc basin, island arc, or a sequence of slab window volcanics. A province-wide geochemical reassessment of the terrane, including new high precision Sr-Pb-Nd-Hf isotope data, has been used to assess the validity of the proposed tectonomagmatic models for the Siletz terrane. The trace element data show little evidence of crustal contamination, or an arc signature, and the samples have rare earth element (REE) patterns that are flat to light REE enriched. These features are similar to other oceanic plateaus such as the Ontong Java and the Caribbean. Initial isotope ratios range from 206Pb/204 Pb: 18.751 to 19.668, 207Pb/204Pb: 15.507 to 15.661, 208Pb/204Pb: 38.294 to 39.2128, 176Hf/177Hf: 0.28300 to 0.28316 (εHf: 9.0 to 14.5), 143Nd/144Nd: 0.51282 to 0.51299 (εNd: 5.0 to 8.1) and 87Sr/86Sr: 0.70302 to 0.70380. These data are consistent with a mantle source of the Siletz terrane that appears to have been heterogeneous and slightly enriched. The enriched signature has characteristics of both EM2 and HIMU components and this, combined with a calculated mantle potential temperature well above ambient mantle, indicates derivation of the Siletz magmatism from a mantle plume, possibly the Yellowstone Hotspot. We therefore conclude that the Siletz terrane represents an accreted oceanic plateau.

  18. Iron isotopic evolution during fractional crystallization of the uppermost Bushveld Complex layered mafic intrusion (United States)

    Bilenker, Laura D.; VanTongeren, Jill A.; Lundstrom, Craig C.; Simon, Adam C.


    We present δ56Fe (56Fe/54Fe relative to standard IRMM-014) data from whole rock and magnetite of the Upper and Upper Main Zones (UUMZ) of the Bushveld Complex. With it, we assess the role of fractional crystallization in controlling the Fe isotopic evolution of a mafic magma. The UUMZ evolved by fractional crystallization of a dry tholeiitic magma to produce gabbros and diorites with cumulus magnetite and fayalitic olivine. Despite previous experimental work indicating a potential for magnetite crystallization to drastically change magma δ56Fe, we observe no change in whole rock δ56Fe above and below magnetite saturation. We also observe no systematic change in whole rock δ56Fe with increasing stratigraphic height, and only a small variation in δ56Fe in magnetite separates above magnetite saturation. Whole rock δ56Fe (errors twice standard deviation, ±2σ) throughout the UUMZ ranges from -0.01 ±0.03‰ to 0.21 ±0.09‰ (δ56FeaverageWR = 0.10 ±0.09‰; n = 21, isotopically light outlier: δ56FeWR = -0.15‰), and magnetites range from 0.28 ±0.04‰ to 0.86 ±0.07‰ (δ56FeaverageMgt = 0.50 ±0.15‰; n = 20), similar to values previously reported for other layered intrusions. We compare our measured δ56FeWR to a model that incorporates the changing normative mineralogy, calculated temperatures, and published fractionation factors of Fe-bearing phases throughout the UUMZ and produces δ56FeWR values that evolve only in response to fractional crystallization. Our results show that the Fe isotopic composition of a multiply saturated (multiple phases on the liquidus) magma is unlikely to change significantly during fractional crystallization of magnetite due to the competing fractionation of other Fe-bearing cumulus phases.

  19. Potassic-ultrapotassic mafic rocks delineate two lithospheric mantle blocks beneath the southern Peruvian Altiplano (United States)

    Carlier, G.; Lorand, J. P.; Liégeois, J. P.; Fornari, M.; Soler, P.; Carlotto, V.; Cárdenas, J.


    The Altiplano of southern Peru displays a large spectrum of Cenozoic potassic (K) and ultrapotassic (UK) mafic rocks that delineate two deep lithospheric mantle blocks that have undergone different depletion and enrichment events. Phlogopite lamproites indicate that the eastern Altiplano block is underlain by a metasomatized harzburgitic mantle of Paleoproterozoic to Archean age (depleted mantle age, TDM = 1130 2485 Ma; ɛNd = -5.0 to -11.4; 87Sr/86Sri = 0.7100 0.7159). Beneath the western Altiplano block, the presence of a younger (TDM = 837 1259 Ma; ɛNd = +0.6 to -6.3; 87Sr/86Sri = 0.7048 0.7069) metasomatized lherzolitic mantle is deduced from multiple occurrences of diopside-rich K-UK lavas (leucitites, leucite-bearing tephrites, olivine, and diopside trachybasalts). A third suite of young (Cusco Vilcanota fault system separating the western and eastern Altiplano blocks; this third suite, composed of diopside-phlogopite lamproites and augite kersantites, minettes, and trachybasalts, sampled a composite mantle source that probably included an asthenospheric component (TDM = 612 864 Ma; ɛNd = -1.1 to -3.5; 87Sr/86Sri = 0.7051 0.7062), in addition to lithospheric components inherited from the eastern and western Altiplano blocks. The spatial distribution of the south Peruvian K-UK magmatism suggests that K-UK melts reached the surface through reuse of older translithospheric weakness zones extending at least to the depth of magma generation. These latter were reactivated by a dextral transpressional regime imposed on the two rigid lithospheric blocks by the Andean orogen.

  20. Origin of Permian extremely high Ti/Y mafic lavas and dykes from Western Guangxi, SW China: Implications for the Emeishan mantle plume magmatism (United States)

    Liu, Xijun; Liang, Qiongdan; Li, Zhenglin; Castillo, Paterno R.; Shi, Yu; Xu, Jifeng; Huang, Xianglin; Liao, Shuai; Huang, Wenlong; Wu, Weinan


    Late Permian mafic flows and dikes are prominent features in and around the Western Guangxi region in southern China. Based on petrographic, geochemical and Sr-Nd isotopic data, the western Guangxi mafic rocks are geochemically akin to the Emeishan large igneous province (ELIP) high-Ti basalts, except that they possess extremely elevated Ti/Y ratios (750-2000). The Dy/Yb and Ti/Y vs. Dy/Dy∗ covariations of the mafic rocks indicate a garnet-controlled magmatic differentiation of a mafic melt at relatively great depth. The limited εNd(t) range from +0.41 to +1.81 also suggests minimal crustal contamination of such a melt. Geochemical modeling using TiO2/Yb vs. Nb/Yb and Zr/Y vs. Nb/Y projections indicate that the parental melts of the western Guangxi mafic rocks formed at a low degree (thick continental lithosphere. Thus, the Guangxi extremely high Ti/Y mafic rocks most likely represent a part of outer zone of the ELIP plume magmatism. Results of this study reinforce the previously proposed temporal and spatial distribution of the ELIP.

  1. Lattice thermal conductivity of silicate glasses at high pressures (United States)

    Chang, Y. Y.; Hsieh, W. P.


    Knowledge of the thermodynamic and transport properties of magma holds the key to understanding the thermal evolution and chemical differentiation of Earth. The discovery of the remnant of a deep magma ocean above the core mantle boundary (CMB) from seismic observations suggest that the CMB heat flux would strongly depend on the thermal conductivity, including lattice (klat) and radiative (krad) components, of dense silicate melts and major constituent minerals around the region. Recent measurements on the krad of dense silicate glasses and lower-mantle minerals show that krad of dense silicate glasses could be significantly smaller than krad of the surrounding solid mantle phases, and therefore the dense silicate melts would act as a thermal insulator in deep lower mantle. This conclusion, however, remains uncertain due to the lack of direct measurements on the lattice thermal conductivity of silicate melts under relevant pressure-temperature conditions. Besides the CMB, magmas exist in different circumstances beneath the surface of the Earth. Chemical compositions of silicate melts vary with geological and geodynamic settings of the melts and have strong influences on their thermal properties. In order to have a better view of heat transport within the Earth, it is important to study compositional and pressure dependences of thermal properties of silicate melts. Here we report experimental results on lattice thermal conductivities of silicate glasses with basaltic and rhyolitic compositions up to Earth's lower mantle pressures using time-domain thermoreflectance coupled with diamond-anvil cell techniques. This study not only provides new data for the thermal conductivity of silicate melts in the Earth's deep interior, but is crucial for further understanding of the evolution of Earth's complex internal structure.

  2. Generation of Continental Crust in Central America: New Field and Geochemical Observations on Silicic Magmatism in Costa Rica (United States)

    Szymanski, D. W.; Patino, L. C.; Vogel, T. A.; Alvarado, G. E.


    section support a model of crystal fractionation, eruption, and mafic replenishment of the magma chamber. Samples range from 60.1 to 70.2 wt.% SiO2, with the most mafic sample occurring at the top of sequence as a visibly mafic-silicic mingled pumice. The Rio Liberia (~1.47 Ma) and Salitral (~1.3 Ma) formations in the Guanacaste region form a series of tuffs, related by the same inferred vent. Despite overlapping silica content, the units have distinct mineral compositions. The Salitral formation includes plagioclase- and amphibole-rich units that appear very similar in the field, while the Rio Liberia contains biotite. Chemically, the units are distinct, forming several separate trends in trace element plots. These heterogeneities most likely reflect differences in both source and/or processes of magma evolution.

  3. Viscosity of Heterogeneous Silicate Melts: A Non-Newtonian Model (United States)

    Liu, Zhuangzhuang; Blanpain, Bart; Guo, Muxing


    The recently published viscosity data of heterogeneous silicate melts with well-documented structure and experimental conditions are critically re-analyzed and tabulated. By using these data, a non-Newtonian viscosity model incorporating solid fraction, solid shape, and shear rate is proposed on the basis of the power-law equation. This model allows calculating the viscosity of the heterogeneous silicate melts with solid fraction up to 34 vol pct. The error between the calculated and measured data is evaluated to be 32 pct, which is acceptable considering the large error in viscosity measurement of the completely liquid silicate melt.

  4. Fire Resistance of Wood Impregnated with Soluble Alkaline Silicates

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    Carlos Alberto Giudice


    Full Text Available The aim of this paper is to determine the fire performance of wood panels (Araucaria angustifolia impregnated with soluble alkaline silicates. Commercial silicates based on sodium and potassium with 2.5/1.0 and 3.0/1.0 silica/alkali molar ratios were selected; solutions and glasses were previously characterized. Experimental panels were tested in a limiting oxygen chamber and in a two-foot tunnel. Results displayed a high fire-retardant efficiency using some soluble silicates.

  5. Assimilation of Consanguineous Mafic Intrutions: Layered Crustal Sill Complexes as Reactive Filters for Continental Basalts (United States)

    Shervais, J. W.; Hanan, B. B.; Vetter, S. K.


    infer that this exchange took place within a 10 km thick mafic sill complex that has been imaged seismically at depths of 12-22 km the middle crust. We propose that this process may apply to a wide range of continental basalts.

  6. Petrogenesis of mafic magmatism in Arabia-Eurasia collision zone: valley filling flows in Armenia (United States)

    Meliksetian, Khachatur; Neill, Iain; Allen, Mark; Navasardyan, Gevorg


    The Turkish- Armenian-Iranian orogenic plateau grew after the Middle Miocene following the initial Paleogene Arabia- Eurasia collision. It is widely accepted, that uplift of the plateau is related to break-off of the southern Neo-Tethys slab beneath the Bitlis-Zagros Suture at ~15-10 Ma, coupled with continued plate convergence and regional crustal shortening. Since this time there has also been a widespread mantle-derived collision magmatism over large parts of NW Iran, Eastern Anatolia and the Lesser Caucasus, potentially hundreds of kilometres from the site of southern Neo-Tethys slab break-off, >10 Myr after the proposed break-off event. Detailed wholer rock geochemistry and Sr-Nd-Pb-Hf isotope data are presented for ~2.5 Ma trachy-basalt to trachy-basaltic andesite lavas erupted in Armenia in the South Caucasus. These thick (up to 400 m) mafic flows generated several plateaux within the Lesser Caucasus: the Javakheti Plateau (S Georgia and NW Armenia), and the Lori and Kotayk Plateaux (Armenia). These basalts sequences also extend to the NE Kars-Erzurum Plateau in eastern Turkey. It is demonstrated that studied series formed by Neo-Tethys slab break-off 300-450 km to the south of the country. It is possible that Late Miocene break-off of a second (northern Neo-Tethys) slab beneath the Pontide Arc allowed asthenospheric upwelling over a much wider area than was affected by southern Neo-Tethyan break-off. Whole-scale delamination of mantle lithosphere can be ruled out due to the modest degrees of partial melting, a lack of asthenospheric components and limited crustal interaction of the Armenian magmas. Small-scale sub-lithospheric convection may be complementary to break-off, causing localised removal of lithospheric mantle and aiding the occurrence of volcanism for a significant time interval after the break-off event(s). Finally, collision magmas such as those in Armenia represent an under-appreciated juvenile addition to continental crust, with extreme

  7. Complexity on a small scale: Emplacement dynamics and evolution of the Doros layered mafic intrusion, Namibia (United States)

    Owen-Smith, Trishya; Ashwal, Lewis


    The Doros Complex in Namibia is a relatively small (~8 km x 4 km), shallow-level layered mafic intrusion that forms part of the ~132 Ma Paraná-Etendeka Large Igneous Province. It consists of a ~500 m-thick preserved sequence of roughly concordant, sill-like gabbro layers dipping in towards the centre of the intrusion, cut by syenitic (bostonite) dykes. The fundamental mineralogy is essentially the same throughout the main package (plagioclase + calcic clinopyroxene + oxy-exsolved Fe-Ti oxides ± olivine), and hence the layering is defined by variations in the modal proportions of these minerals, and in the mineral and rock textures. A detailed petrographic, whole-rock and mineral major and trace element, and Sr-, Nd- and Pb-isotopic study, combined with major element modelling, has shown that the stratigraphic order of appearance of cumulus minerals and overall trends in rock compositions are consistent with fractional crystallisation and accumulation from an uncontaminated basaltic parental magma. However, these data also reveal considerable complexity and stratigraphic trends in mineralogy, chemistry and physical properties incongruent with a simple progressive differentiation path. Based on a comprehensive set of field, petrographic, geochemical and geophysical evidence, we put forward a compelling argument in favour of an origin for the Doros intrusion by multiple, closely-spaced influxes of crystal-bearing magmas (magma mushes), rather than from the post-emplacement differentiation of a single batch of crystal-free melt. This evidence includes intrusive layer relations, textural evidence for primocrysts, disequilibrium features, and stratigraphic reversals in mineral and whole-rock chemistry and magnetic properties. At least seven distinct major injections of magma have been identified in the stratigraphy, as well as several smaller pulses. These findings represent a departure from the traditional single-pulse liquid magma model for the formation of such

  8. Rb-Sr and Nd-Sr isotope geochemistry and petrogenesis of the Misho Mountains mafic dikes (NW Iran

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    Maryam Ahankoub


    Full Text Available Introduction There are some theories about the Paleotethys event during the Paleozoic that have been proposed by geologists (Metcalfe, 2006. Some scientist offered some pieces of evidence about the northern margin of Gondwana (Zhu et al., 2010. The Paleotethys Ocean and Hercynian orogenic report first in Iran, have been Offered from the Morrow and Misho Mountain (Eftekharnejad, 1981. Misho Mountains is located between the north and south Misho faults and cause the formation of a positive flower structure (Moayyed and Hossainzade, 2011. There is theory about Misho southern fault as the best candidate of the Paleotethys suture zone (Moayyed and Hossainzade, 2011. Geochemistry and Sr –Nd isotopic data of the A2 granitic and Synite rocks of the East Misho, indicate that the magmatism post collision has occurred in the active continental margin by extensional zones of the following the closure of the Paleotethys (Ahankoub, 2012. Granite and syenite rocks have been cut by mafic dikes. Mafic dikes are often formed in extensional tectonic settings related to mantle plume or continental break –up (Zhu et al., 2009. In this paper, we use the geochemistry and Nd-Sr isotope data to determined petrogenesis, tectono-magmatic setting and age of Misho mafic dikes. Materials and methods After petrography study of 30 thin sections of mafic dike rocks, 8 samples were selected for whole-rock chemical analyses using ICP-MS and ICP-AES instruments by ACME Company in Vancouver, Canada. We prepared 6 sample For Sm-Nd and Rb-Sr analysis. Sr and Nd isotope ratios were measured with a thermal ionization mass spectrometer, VG Sector 54–30 at the Nagoya University. The isotope abundances of Rb, Sr, Nd, and Sm were measured by the ID method with a Finnigan MAT Thermoquad THQ thermal ionization quadrupole mass spectrometer at the Nagoya University. NBS987 and JNdi-1 were measured as natural Sr and Nd isotope ratio standards (Tanaka et al., 2000. Averages and 2σ errors

  9. Mafic Volcanism Along the Sinaloa Coast, Mexico, and its Relation to the Opening of the Gulf of California (United States)

    Orozco Esquivel, T.; Ferrari, L.; Lopez Martinez, M.


    We report on new localities with mafic volcanism along the Sinaloa coast, which record changes in the magma generation processes along the eastern margin of the Gulf of California. South of Culiacán, Sinaloa, isolated outcrops of basaltic lavas built a ca. 60 km long belt aligned to the SE. The similarity in the mineralogy and composition of the lavas suggest that these outcrops could have been part of a single flow. Lavas contain abundant plagioclase (up to 3 mm), and olivine (up to 1.5 mm) phenocrysts, and scarce clinopyroxene, in a relatively coarse matrix. In multiement diagrams, the lavas show the negative Nb and Ta, and positive Pb and Sr anomalies characteristic of subduction related rocks. The age determination of these rocks is in process, nevertheless, rocks with similar compositions are known from ~11 Ma mafic dikes that outcrop in southern Sinaloa. The Pericos volcanic field, located about 25 km to the NW of Culiacán is composed by lava flows, shield volcanoes, and cinder cones of basaltic composition that cover an area of aprox. 20 x 32 km, and have a well preserved morphology suggestive of a Pliocene-Quaternary age. Lavas are porphyritic and contain olivine, plagioclase and clinopyroxene in a microcrystalline matrix. Some lava flows contain abundant megacrysts of green clinopyroxene (up to 8 cm), olivine (up to 1 cm), and/or plagioclase (up to 1 cm), or aggregates of olivine and clinopyroxene. Trace element abundances are remarkably uniform among all analyzed samples and are characteristic of intraplate magmas. Rocks with very similar composition, mineralogy, and also containing megacrysts, have been reported in the Pliocene Punta Piaxtla and Mesa Cacaxtla, located 200 km to the SSE at the Sinaloa coast. Those similarities indicate that mafic intraplate volcanism related to the opening of the Gulf of California is more broadly represented in the area than previously considered.

  10. Mapping the 3-D extent of the Northern Lobe of the Bushveld layered mafic intrusion from geophysical data (United States)

    Finn, Carol A.; Bedrosian, Paul A.; Cole, Janine; Khoza, Tshepo David; Webb, Susan J.


    Geophysical models image the 3D geometry of the mafic portion of the Bushveld Complex north of the Thabazimbi-Murchison Lineament (TML), critical for understanding the origin of the world's largest layered mafic intrusion and platinum group element deposits. The combination of the gravity and magnetic data with recent seismic, MT, borehole and rock property measurements powerfully constrains the models. The intrusion north of the TML is generally shallowly buried (generally 12,000 m, averaging ∼4000 m. A feeder, suggested by a large modeled thickness (>10,000 m) and funnel shape, for Lower Zone magmas could have originated near the intersection of NS and NE trending TML faults under Mokopane. The TML has been thought to be the feeder zone for the entire Bushveld Complex but the identification of local feeders and/or dikes in the TML in the models is complicated by uncertainties on the syn- and post-Bushveld deformation history. However, modeled moderately thick high density material near the intersection of faults within the central and western TML may represent feeders for parts of the Bushveld Complex if deformation was minimal. The correspondence of flat, high resistivity and density regions reflect the sill-like geometry of the Bushveld Complex without evidence for feeders north of Mokopane. Magnetotelluric models indicate that the Transvaal sedimentary basin underlies much of the Bushveld Complex north of the TML, further than previously thought and important because the degree of reaction and assimilation of the Transvaal rocks with the mafic magmas resulted in a variety of mineralization zones.

  11. Magma generation at a large, hyperactive silicic volcano (Taupo, New Zealand) revealed by U-Th and U-Pb systematics in zircons (United States)

    Charlier, B.L.A.; Wilson, C.J.N.; Lowenstern, J. B.; Blake, S.; van Calsteren, P.W.; Davidson, J.P.


    Young (New Zealand, has involved the development and evacuation of several crustal magmatic systems. Up to and including the 26??5 ka 530 km 3 Oruanui eruption, magmatic systems were contemporaneous but geographically separated. Subsequently they have been separated in time and have vented from geographically overlapping areas. Single-crystal (secondary ionization mass spectrometry) and multiple-crystal (thermal ionization mass spectrometry) zircon model-age data are presented from nine representative eruption deposits from ??? 45 to ???3??5 ka. Zircon yields vary by three orders of magnitude, correlating with the degrees of zircon saturation in the magmas, and influencing the spectra of model ages. Two adjacent magma systems active up to 26??5 ka show wholly contrasting model-age spectra. The smaller system shows a simple unimodal distribution. The larger system, using data from three eruptions, shows bimodal model-age spectra. An older ???100 ka peak is interpreted to represent zircons (antecrysts) derived from older silicic mush or plutonic rocks, and a younger peak to represent zircons (phenocrysts) that grew in the magma body immediately prior to eruption. Post-26??5 ka magma batches show contrasting age spectra, consistent with a mixture of antecrysts, phenocrysts and, in two examples, xenocrysts from Quaternary plutonic and Mesozoic-Palaeozoic metasedimentary rocks. The model-age spectra, coupled with zircon-dissolution modelling, highlight contrasts between short-term silicic magma generation at Taupo, by bulk remobilization of crystal mush and assimilation of metasediment and/or silicic plutonic basement rocks, and the longer-term processes of fractionation from crustally contaminated mafic melts. Contrasts between adjacent or successive magma systems are attributed to differences in positions of the source and root zones within contrasting domains in the quartzo-feldspathic (<15 km deep) crust below the volcano. ?? Oxford University Press, 2004; all

  12. Geochemical characteristics and tectonic setting of the Tuerkubantao mafic-ultramafic intrusion in West Junggar, Xinjiang, China

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    Yufeng Deng


    Full Text Available Mineral chemistry, whole-rock major oxide, and trace element compositions have been determined for the Tuerkubantao mafic-ultramafic intrusion, in order to understand the early Paleozoic tectonic evolution of the West Junggar orogenic belt at the southern margin of the Central Asian orogenic belt. The Tuerkubantao mafic-ultramafic intrusion is a well-differentiated complex comprising peridotite, olivine pyroxenite, gabbro, and diorite. The ultramafic rocks are mostly seen in the central part of the intrusion and surrounded by mafic rocks. The Tuerkubantao intrusive rocks are characterized by enrichment of large ion lithophile elements and depleted high field strength elements relative to N-MORB. In addition, the Tuerkubantao intrusion displays relatively low Th/U and Nb/U (1.13–2.98 and 2.53–7.02, respectively and high La/Nb and Ba/Nb (1.15–4.19 and 37.7–79.82, respectively. These features indicate that the primary magma of the intrusion was derived from partial melting of a previously metasomatized mantle source in a subduction setting. The trace element patterns of peridotites, gabbros, and diorite in the Tuerkubantao intrusion have sub-parallel trends, suggesting that the different rock types are related to each other by differentiation of the same primary magma. The intrusive contact between peridotite and gabbro clearly suggest that the Tuerkubantao is not a fragment of an ophiolite. However, the Tuerkubantao intrusion displays many similarities with Alaskan-type mafic-ultramafic intrusions along major sutures of Phanerozoic orogenic belts. Common features include their geodynamic setting, internal lithological zoning, and geochemistry. The striking similarities indicate that the middle Devonian Tuerkubantao intrusion likely formed in a subduction-related setting similar to that of the Alaskan-type intrusions. In combination with the Devonian magmatism and porphyry mineralization, we propose that subduction of the oceanic slab has

  13. Conversion of rice hull ash into soluble sodium silicate

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    Edson Luiz Foletto


    Full Text Available Sodium silicate is used as raw material for several purposes: silica gel production, preparation of catalysts, inks, load for medicines, concrete hardening accelerator, component of detergents and soaps, refractory constituent and deflocculant in clay slurries. In this work sodium silicate was produced by reacting rice hull ash (RHA and aqueous sodium hydroxide, in open and closed reaction systems. The studied process variables were time, temperature of reaction and composition of the reaction mixture (expressed in terms of molar ratios NaOH/SiO2 and H2O/SiO2. About 90% silica conversion contained in the RHA into sodium silicate was achieved in closed system at 200 °C. The results showed that sodium silicate production from RHA can generate aggregate value to this residue.

  14. Study of thermal effects of silicate-containing hydroxyapatites (United States)

    Golovanova, O. A.; Zaits, A. V.; Berdinskaya, N. V.; Mylnikova, T. S.


    The possibility of modifications of hydroxyapatite silicate ions, from the extracellular fluid prototype solution under near-physiological conditions has been studied. Formation of silicon-structured hydroxyapatite with different extent of substitution of phosphate groups in the silicate group has been established through chemical and X-ray diffraction analyses, FTIR spectroscopy and optical microscopy. The results obtained are in agreement and suggest the possibility of substitution of phosphate groups for silicate groups in the hydroxyapatite structure when introducing different sources of silica, tetraethoxysilane and sodium silicate, in the reaction mixture. Growth in the amount of silicon in Si-HA results in the increase in the thermal stability of the samples. The greatest mass loss occurs at temperatures in the range of 25-400 0C that is caused by the removal of the crystallization and adsorption water and volatile impurities. It is shown that the modified apatites are of imperfect structure and crystallize in a nanocrystalline state.

  15. Silicate Urolithiasis during Long-Term Treatment with Zonisamide

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    Satoru Taguchi


    Full Text Available Silicate urinary calculi are rare in humans, with an incidence of 0.2% of all urinary calculi. Most cases were related to excess ingestion of silicate, typically by taking magnesium trisilicate as an antacid for peptic ulcers over a long period of time; however, there also existed unrelated cases, whose mechanism of development remains unclear. On the other hand, zonisamide, a newer antiepileptic drug, is one of the important causing agents of iatrogenic urinary stones in patients with epilepsy. The supposed mechanism is that zonisamide induces urine alkalinization and then promotes crystallization of urine components such as calcium phosphate by inhibition of carbonate dehydratase in renal tubular epithelial cells. Here, we report a case of silicate urolithiasis during long-term treatment with zonisamide without magnesium trisilicate intake and discuss the etiology of the disease by examining the silicate concentration in his urine.

  16. Tris (catecholato) silicates of nickel: Synthesis, characterization and ...

    Indian Academy of Sciences (India)

    catecholato)silicates of nickel: Synthesis, characterization and first observation of inter-ion ligand transfer. J Vijeyakumar Kingston G S M Sundaram M N Sudheendra Rao. Volume 112 Issue 3 June 2000 pp 402-402 ...

  17. Conversion of rice hull ash into soluble sodium silicate


    Edson Luiz Foletto; Ederson Gratieri; Leonardo Hadlich de Oliveira; Sérgio Luiz Jahn


    Sodium silicate is used as raw material for several purposes: silica gel production, preparation of catalysts, inks, load for medicines, concrete hardening accelerator, component of detergents and soaps, refractory constituent and deflocculant in clay slurries. In this work sodium silicate was produced by reacting rice hull ash (RHA) and aqueous sodium hydroxide, in open and closed reaction systems. The studied process variables were time, temperature of reaction and composition of the reacti...

  18. Comparison of silicon nanoparticles and silicate treatments in fenugreek. (United States)

    Nazaralian, Sanam; Majd, Ahmad; Irian, Saeed; Najafi, Farzaneh; Ghahremaninejad, Farrokh; Landberg, Tommy; Greger, Maria


    Silicon (Si) fertilization improves crop cultivation and is commonly added in the form of soluble silicates. However, most natural plant-available Si originates from plant formed amorphous SiO2 particles, phytoliths, similar to SiO2-nanoparticles (SiNP). In this work we, therefore, compared the effect by sodium silicate and that of SiNP on Si accumulation, activity of antioxidative stress enzymes catalase, peroxidase, superoxide dismutase, lignification of xylem cell walls and activity of phenylalanine ammonia-lyase (PAL) as well as expression of genes for the putative silicon transporter (PST), defensive (Tfgd 1) and phosphoenolpyruvate carboxykinase (PEPCK) and protein in fenugreek (Trigonella foenum-graecum L.) grown in hydroponics. The results showed that Si was taken up from both silicate and SiNP treatments and increasing sodium silicate addition increased the translocation of Si to the shoot, while this was not shown with increasing SiNP addition. The silicon transporter PST was upregulated at a greater level when sodium silicate was added compared with SiNP addition. There were no differences in effects between sodium silicate and SiNP treatments on the other parameters measured. Both treatments increased the uptake and accumulation of Si, xylem cell wall lignification, cell wall thickness, PAL activity and protein concentration in seedlings, while there was no effect on antioxidative enzyme activity. Tfgd 1 expression was strongly downregulated in leaves at Si addition. The similarity in effects by silicate and SiNP would be due to that SiNP releases silicate, which may be taken up, shown by a decrease in SiNP particle size with time in the medium. Copyright © 2017 Elsevier Masson SAS. All rights reserved.

  19. Effects of silicate application on soil fertility and wheat yield

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    Marcos Vinícius Mansano Sarto


    Full Text Available An improvement in soil chemical properties and crop development with silicate application has been confirmed in several plant species. The effects of silicate application on soil chemical properties and wheat growth were investigated in the present study. The experiment was carried out in 8-L plastic pots in a greenhouse. Treatments were arranged in a randomized block design in a 3 × 5 factorial: three soils [Rhodic Acrudox (Ox1, Rhodic Hapludox (Ox2 and Arenic Hapludult (Ult] and five silicate rates (0, 1, 2, 4 and 6 Mg ha–1 of calcium/magnesium silicate, with four replications. The plant length, number of spikes per pot, shoot dry matter and grain yield, were measured after 115 days of wheat (Triticum aestivum L. growth. Changes in the soil chemical properties (pH, H+ + Al3+, Al3+, P, K, Ca, Mg, Si, Cu, Zn, Fe and Mn were analyzed after wheat harvest. Application of calcium/magnesium silicate reduces the potential acidity (H+ + Al3+ and Al3+ phytotoxic; and increases the soil pH, available Ca, Mg and Si, cation exchange capacity (CEC and soil base saturation. Silicate application did not affect the available P, exchangeable K and availability of micronutrients (Cu, Zn, Fe and Mn in the three soils. The application of calcium/magnesium silicate in an acid clayey Rhodic Hapludox improves the development and yield of wheat; however, the silicate application in soil with pH higher to 5.3 and high Si availability does not affect the agronomic characteristics and grain yield of wheat. 

  20. History of Nebular Processing Traced by Silicate Stardust in IDPS (United States)

    Messenger, Scott R.; Keller, L. P.; Nakamura-Messenger, K.


    Chondritic porous interplanetary dust particles (CP-IDPs) may be the best preserved remnants of primordial solar system materials, in part because they were not affected by parent body hydrothermal alteration. Their primitive characteristics include fine grained, unequilibrated, anhydrous mineralogy, enrichment in volatile elements, and abundant molecular cloud material and silicate stardust. However, while the majority of CP-IDP materials likely derived from the Solar System, their formation processes and provenance are poorly constrained. Stardust abundances provide a relative measure of the extent of processing that the Solar System starting materials has undergone in primitive materials. For example, among primitive meteorites silicate stardust abundances vary by over two orders of magnitude (less than 10-200 ppm). This range of abundances is ascribed to varying extents of aqueous processing in the meteorite parent bodies. The higher average silicate stardust abundances among CP-IDPs (greater than 375 ppm) are thus attributable to the lack of aqueous processing of these materials. Yet, silicate stardust abundances in IDPs also vary considerably. While the silicate stardust abundance in IDPs having anomalous N isotopic compositions was reported to be 375 ppm, the abundance in IDPs lacking N anomalies is less than 10 ppm. Furthermore, these values are significantly eclipsed among some IDPs with abundances ranging from 2,000 ppm to 10,000 ppm. Given that CP-IDPs have not been significantly affected by parent body processes, the difference in silicate stardust abundances among these IDPs must reflect varying extents of nebular processing. Here we present recent results of a systematic coordinated mineralogical/isotopic study of large cluster IDPs aimed at (1) characterizing the mineralogy of presolar silicates and (2) delineating the mineralogical and petrographic characteristics of IDPs with differing silicate stardust abundances. One of the goals of this study is

  1. High-pressure mafic oceanic rocks from the Makbal Complex, Tianshan Mountains (Kazakhstan & Kyrgyzstan): Implications for the metamorphic evolution of a fossil subduction zone (United States)

    Meyer, Melanie; Klemd, Reiner; Konopelko, Dmitry


    The Makbal Complex in the western Tianshan Mountains of Kazakhstan and Kyrgyzstan consists of HP/UHP metasedimentary host rocks which enclose various HP mafic blocks or boudins. These mafic rocks comprise rare eclogites (sensu stricto and sensu lato), garnet amphibolites (retrograded eclogites) and a newly discovered glaucophanite (glaucophane-garnet-omphacite bearing rock). So far the Makbal Complex has been interpreted to predominantly consist of continental lithologies and the mafic rocks were considered as dismembered dikes intruding continental metasediments. This interpretation is mainly based on the geological relationship and bulk rock chemistry of the different rock types. It was further suggested that the continental lithologies of the Makbal Complex underwent eclogite-facies metamorphism in a former subduction zone. In the present study we combined conventional geothermometry, P-T pseudosection modeling and major and trace element whole rock geochemistry for different mafic samples (glaucophanite and eclogites (sensu lato)) in order to shed light on both the metamorphic evolution and the protoliths of the mafic HP rocks in the Makbal Complex. Prograde to peak-pressure clockwise P-T paths of glaucophanite and eclogites (sensu lato) were modeled using garnet isopleth thermobarometry. The results show that the glaucophanite and eclogite (sensu lato) samples experienced similar prograde P-T paths and slightly different peak metamorphic conditions at ~ 560 °C at 2.4 GPa for the former and between ~ 520 °C at 2.2 GPa and ~ 555 °C at ~ 2.5 GPa for the latter, corresponding to burial depths between 70 and 85 km. Whole rock major and trace element analyses and petrological evidence imply that the various rock types at the Makbal Complex most likely originated from different precursor rocks. Eclogites (sensu lato) are believed to represent strongly retrogressed former eclogite-facies rocks that had never been eclogites (sensu stricto, i.e. > 70 vol.% garnet and

  2. Silicates in orthopedics and bone tissue engineering materials. (United States)

    Zhou, Xianfeng; Zhang, Nianli; Mankoci, Steven; Sahai, Nita


    Following the success of silicate-based glasses as bioactive materials, silicates are believed to play important roles in promoting bone formation and have therefore been considered to provide a hydroxyapatite (HAP) surface layer capable of binding to bone as well as potentially being a pro-osteoinductive factor. Natural silicate minerals and silicate-substituted HAPs are also being actively investigated as orthopaedic bone and dental biomaterials for application in tissue engineering. However, the mechanisms for the proposed roles of silicate in these materials have not been fully understood and are controversial. Here, we review the potential roles of silicate for bone tissue engineering applications and recent breakthroughs in identifying the cellular-level molecular mechanisms for the osteoinductivity of silica. The goal of this article is to inspire new ideas for the rational design of third-generation cell-and gene-affecting biomaterials. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 2090-2102, 2017. © 2017 Wiley Periodicals, Inc.

  3. On the Mg/Fe Ratio in Silicate Minerals in the Circumstellar Environments I. The Mg/Fe Ratio in Silicate Mineral Constituents of the Kaba Meteorite (United States)

    Futó, P.


    The moderately high ratio of Mg in the silicates of the solar environment indicates that Mg-rich silicates are likely to be frequent in the interstellar medium and the circumstellar environments in case of chondritic-like composition.

  4. Potassium silicate and calcium silicate on the resistance of soybean to Phakopsora pachyrhizi infection

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    Maria Fernanda Cruz


    Full Text Available The control of Asian Soybean Rust (ASR, caused by Phakopsora pachyrhizi, has been difficult due to the aggressiveness of the pathogen and the lack of resistant cultivars. The objective of this study was to evaluate the effects of spray of potassium silicate (PS and soil amendment with calcium silicate (CS on soybean resistance to ASR. The PS solution was sprayed to leaves 24 hours prior to fungal inoculation while CS was amended to the soil at thirty-five days before sowing. The infection process of P. pachyrhizi was investigated by scanning electron microscopy. The uredia on leaves of plants sprayed with PS were smaller and more compact than those observed on the leaves of plants grown in soil amended with CS or in soil non-amended with CS (control treatment. On leaves of plants from the control treatment, uredia produced many urediniospores at 9 days after inoculation, and the ASR severity was 15, 8 and 9%, respectively, for plants from control, PS and CS treatments. In conclusion, the spray of PS contributed to reduce the number of uredia per cm² of leaf area and both PS spray and CS resulted in lower ASR symptoms.

  5. Role of mafic and ultramafic rocks in drinking water quality and its potential health risk assessment, Northern Pakistan. (United States)

    Begum, Shaheen; Shah, Mohammad Tahir; Muhammad, Said; Khan, Sardar


    This study investigates the drinking water (groundwater and surface water) quality and potential risk assessment along mafic and ultramafic rocks in the Swat district of Khyber Pakhtunkhwa Provence, Pakistan. For this purpose, 82 groundwater and 33 surface water samples were collected and analyzed for physico-chemical parameters. Results showed that the majority of the physico-chemical parameters were found to be within the drinking water guidelines set by the World Health Organization. However, major cationic metals such as magnesium (Mg), and trace metals (TM) including iron (Fe), manganese (Mn), nickel (Ni), chromium (Cr) and cobalt (Co) showed exceeded concentrations in 13%, 4%, 2%, 20%, 20% and 55% of water samples, respectively. Health risk assessment revealed that the non-carcinogenic effects or hazard quotient values through the oral ingestion pathway of water consumption for the TM (viz., Fe, Cr and Mn) were found to be greater than 1, could result in chronic risk to the exposed population. Results of statistical analyses revealed that mafic and ultramafic rocks are the main sources of metal contamination in drinking water, especially Ni and Cr. Both Ni and Cr have toxic health effects and therefore this study suggests that contaminated sites should be avoided or treated for drinking and domestic purposes.

  6. Viscoelastic properties of polymer based layered-silicate nanocomposites (United States)

    Ren, Jiaxiang

    Polymer based layered-silicate nanocomposites offer the potential for dramatically improved mechanical, thermal, and barrier properties while keeping the material density low. Understanding the linear and non-linear viscoelastic response for such materials is crucial because of the ability of such measurements to elucidate the mesoscale dispersion of layered-silicates and changes in such dispersion to applied flows as would be encountered in processing of these materials. A series of intercalated polystyrene (and derivatives of polystyrene) layered-silicate nanocomposites are studied to demonstrate the influence of mesoscale dispersion and organic---inorganic interactions on the linear and non-linear viscoelastic properties. A layered-silicate network structure is exhibited for the nanocomposites with strong polymer-silicate interaction such as montmorillonite (2C18M) and fluorohectorite (C18F) and the percolation threshold is ˜ 6 wt % for the 2C18M based hybrids. However, the nanocomposites based on hectorite (2C18H) with weak polymer-silicate interaction exhibit liquid-like terminal zone behavior. Furthermore, the enhanced terminal zone elastic modulus and viscosity of high brominated polystyrene and high molecular weight polystyrene based 2C18M nanocomposites suggest an improved delamination and dispersion of layered-silicates in the polymer matrix. The non-linear viscoelastic properties, specifically, the non-linear stress relaxation behavior and the applicability of time---strain separability, the effect of increasing strain amplitude on the oscillatory shear flow properties, and the shear rate dependence of the steady shear flow properties are examined. The silicate sheets (or collections of sheets) exhibit the ability to be oriented by the applied flow. Experimentally, the empirical Cox - Merz rule is demonstrated to be inapplicable for the hybrids. Furthermore, the K-BKZ constitutive model is used to model the steady shear properties. While being able to


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    Full Text Available The objective of the submitted work was to prepare and to characterize two types of silicate coatings prepared by the sol-gel method using the dip-coating technique on a titanium substrate. Efforts have been made to use mechanical properties of bio-inert titanium and bioactive properties of a silicate layer enriched with an admixture of compounds identified below. The first group consisted of silicate coatings containing silver, brushite and monetite. The other group of silicate coatings contained calcium nitrate and triethyl phosphate. Mechanically and chemically treated titanium substrates were dipped into sols and dried and fired. Silicate coatings from the first group were also chemically treated in 10 mol.l-1 solution of sodium hydroxide. All coatings were measured to determine their adhesive and bioactive properties and furthermore the antibacterial properties were tested in the case of first group. Surfaces of the coated substrates were investigated after the firing and after the individual tests with optical and electron microscopy and X-ray microdiffraction. A tape test demonstrated excellent adhesive property of all coatings to the substrate, classified with degree 5. A static in vitro test demonstrated bioactivity of nearly all the coatings. The basic silicate coating from the first group and one type of coating from the second group were identified as inert. Antibacterial properties of silicate coatings containing silver showed to be different when tested against Escherichia coli bacteria. A complete inhibition of the growth of bacteria under our experimental conditions was observed for the coating containing silver and monetite and a partial inhibition of the growth of bacteria for coatings containing silver and silver in combination with brushite.

  8. Geologic Evolution of the Sierra de Nanchititla Silicic Volcanic Center, Southern Mexico (United States)

    Gonzalez, N.; Ferrari, L.; Lopez, M.; Cerca, M.; Orozco, M.


    The Sierra de Nanchititla Volcanic Center (SNVC) is located at the borders of the States of Mexico, Michoacán and Guerrero, in the northern sector of Sierra Madre del Sur magmatic province (SMS) of México. Previous studies in the areas of Taxco and Tilzapotla recognized an Early Tertiary brittle deformation along WNW-ESE to NW-SE trending strike slip fault systems at the north of the SMS (Alaniz-Alvarez et al., 2002, JVGR; Morán-Zenteno et al., 2005, JVGR). This fault systems apparently favored the emplacement of several silicic volcanic centers aligned in a WNW-ESE direction during the Eocene and earliest Oligocene. These volcanic centers include Huatla, Tilzapotla, Taxco, La Goleta and Sierra de Nanchititla. We carried out a detailed geologic study of the SNVC backed by Ar/Ar geochronology and trace element geochemistry. Our results indicate that the SNVC is part of the Eocene magmatic episode recorded in the SMS. The first volcanic rocks in the area are basaltic-andesitic lavas dated at ~42 Ma. However, the activity of the SNVC proper is concentrated between 37.8±0.2 and 35.6±0.5 Ma and was characterized by the emplacement of rhyolitic sub-volcanic bodies (cryptodomes), voluminous pyroclastic deposits and endogenous domes. The oldest magmatic event is the intrusion of WNW-ESE-trending mafic aphyric dikes dated 35.6±0.5 Ma that fed the Puerto El Salitre andesite. Magmatic activity continued with the emplacement of cryptodomes with sub-volcanic texture. The main phase of the SNVC took place in late Eocene with the emplacement of three units: (1) WNW-ESE-trending felsic pyroclastic dikes feeding the large Nanchititla Ignimbrite (35.6±0.5 Ma), (2) rhyolitic domes with vents aligned in a WNW-ESE direction (35.6±0.1 Ma), the and (3) a pyroclastic flow (Tequezquite Ignimbrite) likely vented from a dome. Geochemical data are consistent with a differentiation process, starting with primary mafic magmas and originating both basaltic- andesitic and andesitic rocks

  9. SON68 glass dissolution driven by magnesium silicate precipitation

    Energy Technology Data Exchange (ETDEWEB)

    Fleury, Benjamin, E-mail: [CEA Marcoule, DEN/DTCD/SECM/LCLT, BP17171, 30207 Bagnols-sur-cèze (France); Godon, Nicole [CEA Marcoule, DEN/DTCD/SECM/LCLT, BP17171, 30207 Bagnols-sur-cèze (France); Ayral, André [IEM, University Montpellier 2, CC 047, Place Eugène Bataillon, 34095 Montpellier Cedex 5 (France); Gin, Stéphane [CEA Marcoule, DEN/DTCD/SECM/LCLT, BP17171, 30207 Bagnols-sur-cèze (France)


    Experimental results are reported on the effect of magnesium silicate precipitation on the mechanisms and rate of borosilicate glass dissolution. Leaching experiments with SON68 glass, a borosilicate containing no Mg, were carried out in initially deionized water at 50 °C with a glass-surface-area-to-solution-volume ratio of 20,000 m{sup −1}. After 29 days of alteration the experimental conditions were modified by the addition of Mg to trigger the precipitation of Mg-silicate. Additional experiments were conducted to investigate the importance of other parameters such as pH or dissolved silica on the mechanisms of precipitation of Mg-silicates and their consequences on the glass dissolution rate. Mg-silicates precipitate immediately after Mg is added. The amount of altered glass increases with the quantity of added Mg, and is smaller when silicon is added in solution. A time lag is observed between the addition of magnesium and the resumption of glass alteration because silicon is first provided by partial dissolution of the previously formed alteration gel. It is shown that nucleation does not limit Mg-silicate precipitation. A pH above 8 is necessary for the phase to precipitate under the investigated experimental conditions. On the other hand the glass alteration kinetics limits the precipitation if the magnesium is supplied in solution at a non-limiting rate.

  10. Heterogeneous nucleation of protein crystals on fluorinated layered silicate.

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    Keita Ino

    Full Text Available Here, we describe an improved system for protein crystallization based on heterogeneous nucleation using fluorinated layered silicate. In addition, we also investigated the mechanism of nucleation on the silicate surface. Crystallization of lysozyme using silicates with different chemical compositions indicated that fluorosilicates promoted nucleation whereas the silicates without fluorine did not. The use of synthesized saponites for lysozyme crystallization confirmed that the substitution of hydroxyl groups contained in the lamellae structure for fluorine atoms is responsible for the nucleation-inducing property of the nucleant. Crystallization of twelve proteins with a wide range of pI values revealed that the nucleation promoting effect of the saponites tended to increase with increased substitution rate. Furthermore, the saponite with the highest fluorine content promoted nucleation in all the test proteins regardless of their overall net charge. Adsorption experiments of proteins on the saponites confirmed that the density of adsorbed molecules increased according to the substitution rate, thereby explaining the heterogeneous nucleation on the silicate surface.

  11. Silicate fertilizer and irrigation depth in corn production

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    Edvaldo Eloy Dantas Júnior


    Full Text Available Calcium-magnesium silicates improve the soil physicochemical properties and provide benefits to plant nutrition, since they are sources of silica, calcium and magnesium. The objective of this study was to evaluate the grain yield of irrigated corn fertilized with calcium-magnesium silicate. The experiment was carried out in a greenhouse in Campina Grande - PB, Brazil, using plastic pots containing 80 kg of soil. The treatments consisted of the combination of four irrigation depths, related to water replacement of 50, 75, 100 and 125% of the crop evapotranspiration, with fertilizer levels of 0, 82, 164 and 246 g of calcium-magnesium silicate, with three replications. The experimental design was in randomized blocks, with the irrigation depths distributed in bands while the silicon levels constituted the subplots. Corn yield was influenced by calcium-magnesium silicate and by irrigation depth, obtaining the greatest grain yield with the dose of 164 g pot-1 irrigated at the highest water level. The water-use efficiency of in corn production tended to decrease when the irrigation depth was increased. The best water-use efficiency was observed when the irrigation level was between 87 and 174 mm, and the dose of silicate was 164 g pot-1.

  12. Diverse Mafic Influences on the Magmatic System of the 2.08 Ma Huckleberry Ridge Eruption, Yellowstone (United States)

    Wilson, C. J. N.; Swallow, E. J.; Charlier, B. L. A.; Gamble, J. A.


    The Yellowstone Plateau Volcanic Field (YPVF) is the youngest, currently active focus of the long-lived Yellowstone-Snake River Plain (YSRP) volcanic province. This province is traditionally considered to be bimodal1, with mantle-derived olivine tholeiites providing the thermal and volatile fluxes to generate the voluminous rhyolitic volcanism that forms the initial stages at each caldera focus2. There are also lesser volumes of alkalic compositions, which define a Craters of the Moon (COM) trend1. These eruptives, dominantly trachy-basalts and -andesites but continuous to high-Ba rhyolites, are often found at the margins of the YSRP and are believed to represent small-volume magma batches derived by extreme mid-crustal fractionation of a tholeiitic parent3,4. The 2,500 km3 Huckleberry Ridge Tuff (HRT), the first of three caldera-forming eruptions at the YPVF, consists of minor fall deposits followed by three voluminous ignimbrite members: A, B and C4. The HRT was preceded and followed by the eruption of YSRP olivine tholeiites within and around the inferred caldera4. Previously identified4 aphyric scoria in HRT member B, and a newly identified juvenile mafic component in HRT member A, are however more extreme in composition than the COM magma type with SiO2 of 49.3- 59.0 wt %, Na2O+K2O 4.5-6.6 wt %, Ba to 3500 ppm, Zr to 1850 ppm and P2O5 to 1.8 wt %. This `HRT-COM' trend is parallel to but offset to higher Ba from that defined by younger surficial COM-type lava flows west of the HRT caldera. We here summarise major, trace and isotopic data from these three mafic lineages, which temporally encompass the HRT. We compare them with other data of the COM suite and evaluate interpretations for their source which range from extreme fractional crystallisation to melts from metasomatised mantle. We highlight the close spatial and temporal association of the mafic lineages, despite their distinct chemical signatures, indicating the presence of complex root zones

  13. Geochronologic and geochemical constraints of the petrogenesis of Permian mafic dykes in the Wuding area, SW China: Implications for Fe-Ti enrichment in mafic rocks in the ELIP (United States)

    Fan, Hong-Peng; Zhu, Wei-Guang; Bai, Zhong-Jie; Yang, Yi-Jin


    Mafic dykes are widely distributed and well preserved in the Wuding area, SW China. The dykes are composed of fine-grained diabases, which are further subdivided into two groups (Group I and Group II). The rocks from Group I have relatively higher MgO (4.95-6.16 wt%) and lower TiO2 (2.26-2.78 wt%) contents than those from the Group II rocks (MgO = 4.04-4.58 wt%; TiO2 = 4.09-4.55 wt%). Two baddeleyite ages of 264 ± 3 Ma and 256 ± 5 Ma from the Wuding dykes suggest that the ages of these dykes are similar to the plutonic bodies and the associated volcanic rocks of the Emeishan large igneous province (ELIP). The compositions and isotopic signatures of the dykes are also similar to those of the ELIP volcanic rocks, indicating derivation from the same magmatic event at 260 Ma. The primary melts of the Wuding dykes were originated by partial melting of a long-term depleted OIB-like mantle source. The Group I dykes were mainly formed by wallrock assimilation and fractional crystallization processes. The magmas parental to the Group II rocks were much more evolved than the magma parental to the Group I rocks and probably produced by wallrock assimilation and fractional crystallization of the parent magma of the Group I rocks. The increasing enrichment of Fe and Ti from the Group I to the Group II rocks were attributed to a fractional crystallization process which may be an epitome of enrichment of Fe and Ti in the Fe-Ti rich mafic intrusions of the ELIP.

  14. Steam based conversion coating on AA6060 alloy: Effect of sodium silicate chemistry and corrosion performance (United States)

    Din, Rameez Ud; Bordo, Kirill; Tabrizian, Naja; Jellesen, Morten Stendahl; Ambat, Rajan


    Surface treatment of aluminium alloy AA6060 using an industrially applicable pilot steam jet system with and without silicate chemistry has been investigated. Treatment using steam alone and steam with silicate, resulted in an oxide layer formation with thickness ∼425 nm and ∼160 nm, respectively. Moreover, the use of sodium silicate resulted in the formation of distinct microstructure and incorporation of silicate into the oxide film. These oxide films reduced the anodic activity 4 times, while the corrosion protection by silicate containing oxide was the function of its concentration. Further, in acid salt spray and filiform corrosion tests, oxide layer containing silicate exhibited two times higher corrosion resistance.

  15. Copper Containing Silicates as Catalysts for Liquid Phase Cyclohexane Oxidation

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    Cruz Rosenira S. da


    Full Text Available Copper containing silicates have been prepared by an acid-catalyzed sol-gel process. The materials were characterized by X-ray diffraction and fluorescence, EPR spectroscopy, elemental analysis, N2-physisorption, thermogravimetry, differential scanning calorimetry, temperature-programmed reduction, FTIR and UV/VIS spectroscopy. The silicates were shown to be efficient catalysts for the oxidation of cyclohexane with tert-butyl hydroperoxide as oxidant. Cyclohexanol and cyclohexanone were obtained as the main products. The metal was shown to be weakly bound to the silicate matrix and metal leaching was observed. Leaching was quantified by X-ray fluorescence and leaching tests showed that the catalytic activity is due to supported copper species. Leached copper showed no activity in the homogeneous phase.

  16. Rubber curing chemistry governing the orientation of layered silicate

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    Full Text Available The effect of curing systems on the orientation and the dispersion of the layered silicates in acrylonitrile butadiene rubber nanocomposite is reported. Significant differences in X-ray diffraction pattern between peroxide curing and sulfur curing was observed. Intense X-ray scattering values in the XRD experiments from peroxide cured vulcanizates indicate an orientation of the layers in a preferred direction as evinced by transmission electron micrographs. However, sulfur cured vulcanizates show no preferential orientation of the silicate particles. Nevertheless, a closer inspection of transmission electron microscopy (TEM images of peroxide and sulfur cured samples shows exfoliated silicate layers in the acrylonitrile butadiene rubber (NBR matrix. It was revealed in the prevailing study that the use of an excess amount of stearic acid in the formulation of the sulfur curing package leads to almost exfoliated type X-ray scattering pattern.

  17. Petrophysical Analysis of Siliceous Ooze Sediments, Ormen Lange Field, Norway

    DEFF Research Database (Denmark)

    Awedalkarim, Ahmed; Fabricius, Ida Lykke

    structure is complex and the solids are mechanically fragile and hydrous. Normal petrophysical methods used in formation evaluation might not be suitable for interpreting siliceous ooze. For example, density and neutron logging tools are calibrated to give correct porosity readings in a limestone formation...... to analyse and interpret logging data acquired through siliceous ooze sediments. Our main objectives were to characterize and evaluate the petrophysics of siliceous ooze and to find the true porosity and water saturation to test its hydrocarbon reservoir potential. We used and integrated core analysis data...... with logging data from four Ormen Lange wells, and included X-ray diffraction analysis (XRD) data. Additionally, other available information such as petrographic thin-section analysis, core computed tomography scans (CT-scans), scanning electron microscope (SEM), and other published data were used here...

  18. Potential of calcium silicate to mitigate water deficiency in maize

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    Douglas José Marques


    Full Text Available ABSTRACT The aim of this study was to evaluate the potential of calcium silicate to mitigate the effects of water deficiency in maize plants yield. A completely randomized factorial design, consisting of five combinations of calcium silicate (0, 25, 50, 75, and 100% and five different soil moisture levels (30, 70, 100, 130, and 160%, was adopted. The following parameters were evaluated: soil matric potential, xylem water potential, silicon concentration, leaf dry weight, and dry mass production. Matric potential monitoring confirmed that the irrigation depths employed resulted in different environments for maize plant development during the experiment. Confirming the hypothesis of the study, at the lower irrigation depths, the maize production has accompanied the increase in calcium silicate used as corrective up to the proportion of 50%. These results indicate that silicon mitigated the impact of water deficiency in maize plants and increased the xylem water potential.

  19. Energetic Processing of Interstellar Silicate Grains by Cosmic Rays

    Energy Technology Data Exchange (ETDEWEB)

    Bringa, E M; Kucheyev, S O; Loeffler, M J; Baragiola, R A; Tielens, A G Q M; Dai, Z R; Graham, G; Bajt, S; Bradley, J; Dukes, C A; Felter, T E; Torres, D F; van Breugel, W


    While a significant fraction of silicate dust in stellar winds has a crystalline structure, in the interstellar medium nearly all of it is amorphous. One possible explanation for this observation is the amorphization of crystalline silicates by relatively 'low' energy, heavy ion cosmic rays. Here we present the results of multiple laboratory experiments showing that single-crystal synthetic forsterite (Mg{sub 2}SiO{sub 4}) amorphizes when irradiated by 10 MeV Xe{sup ++} ions at large enough fluences. Using modeling, we extrapolate these results to show that 0.1-5.0 GeV heavy ion cosmic rays can rapidly ({approx}70 Million yrs) amorphize crystalline silicate grains ejected by stars into the interstellar medium.

  20. Seismic constraints on a large mafic intrusion with implications for the subsidence mechanism of the Danish Basin

    DEFF Research Database (Denmark)

    Sandrin, Alessandro; Thybo, Hans


    Seismic refraction data from the ESTRID-1 profile are used for seismic velocity modeling along the strike of a large mafic intrusion in the Norwegian-Danish Basin, central Denmark. The P wave velocity structure identifies a ~8 km thick sedimentary succession with velocities between 1.8 and 5.7 km...... the magma probably intruded during only a few events and other similar structures cover much of the basin. An anomalously high velocity gradient (from 7.0 km/s in the middle crust to 7.7 km/s at 30-32 km depth) in the central part of the intrusion coincides with an interval without Moho reflections...

  1. Main characteristics and review of mineral resources of the Kabanga-Musongati mafic-ultramafic alignment in Burundi (United States)

    Deblond, A.; Tack, L.


    The first part of this paper gives the main characteristics of the Kabanga-Musongati (KM) mafic-ultramafic alignment in Burundi. This 350 km long alignment, with an emplacement age of 1275±11 Ma (UPb on zircon), extends from Burundi to Uganda. In Burundi, where the KM alignment consists of nine main massifs, a petrological study has defined stratigraphical units comparable to those identified in other layered igneous massifs, such as the Great Dyke of Zimbabwe and the Bushveld Complex in South Africa. The second part of this paper deals with the metallogeny of the KM alignment in Burundi. A review of the well-known deposits is given. Their stratigraphical position and likely origin are discussed in the light of petrological results. New data on platinum group elements (PGE) are provided. Finally, pathways for future mineral exploration are proposed, in particular for PGE-rich sulphides.

  2. Potassium Silicate Foliar Fertilizer Grade from Geothermal Sludge and Pyrophyllite

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    Muljani Srie


    Full Text Available Potassium silicate fertilizer grade were successfully produced by direct fusion of silica (SiO2 and potasium (KOH and K2CO3 in furnaces at temperatures up to melting point of mixture. The geothermal sludge (98% SiO2 and the pyrophyllite (95% SiO2 were used as silica sources. The purposes of the study was to synthesise potassium silicate fertilizer grade having solids concentrations in the range of 31-37% K2O, and silica in the range of 48-54% SiO2. The weight ratio of silicon dioxide/potasium solid being 1:1 to 5:1. Silica from geothermal sludge is amorphous, whereas pyrophylite is crystalline phase. The results showed that the amount of raw materials needed to get the appropriate molar ratio of potassium silicate fertilizer grade are different, as well as the fusion temperature of the furnace. Potassium silicate prepared from potassium hydroxide and geothermal sludge produced a low molar ratio (2.5: 1 to 3: 1. The potassium required quite small (4:1 in weight ratio, and on a fusion temperature of about 900 °C. Meanwhile, the potassium silicate prepared from pyrophyllite produced a high molar ratio (1.4 - 9.4 and on a fusion temperature of about 1350 °C, so that potassium needed large enough to meet the required molar ratio for the fertilizer grade. The product potassium silicate solid is amorphous with a little trace of crystalline.

  3. The origin of spheroidal patterns of weathering in the Pados-Tundra mafic-ultramafic complex, Kola Peninsula, Russia

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    A.Y. Barkov


    Full Text Available We document a new and unusual occurrence of patterns of protruding spheroidal weathering developed in a dunitic rock of the Pados-Tundra mafic-ultramafic complex of Early Proterozoic age, Kola Peninsula, Russia. It provides an example similar to that reported recently from a mineralized harzburgite in the Monchepluton layered complex in the same region. These patterns are genetically different from common results of “normal spheroidal weathering” sensu stricto. The spheroidally weathered dunite at Pados-Tundra consists of a high-Fo olivine, Ol (Fo 87. 5, which is, in fact, not altered. Accessory grains of aluminous chromite are present. Relief spheroids (1.5 to 4 cm in diameter; up to ~5 vol. % are distributed sparsely and heterogeneously. They are hosted by the olivine matrix and composed of talc, Tlc, and tremolite, Tr, (Mg# = 95-96 formed presumably at the expense of orthopyroxene, Opx, (i.e., pre-existing oikocrysts during a deuteric (autometasomatic alteration. In contrast, oikocrystic Opx (En 86.0 is quite fresh in related spheroids at Monchepluton, in which only minor deuteric alteration (Tlc + Tr are observed. We infer that (1 the ball-shaped morphology of the weathered surface is a reflection of the presence of oikocrysts of Opx, which crystallized after Ol at the magmatic stage; they were entirely replaced by the deuterically induced Tlc + Tr at Pados-Tundra. (2 Differential rates of weathering are implied for rock-forming minerals in these ultramafic rocks, with a higher resistance of Opx vs. Fo-rich Ol, and Tlc + Tr vs. Fo-rich Ol. (3 The ball-like shape of the large spheroids, produced by magmatic processes, may likely represent an additional factor of their higher stability to weathering in the superficial environment. Similar patterns can be expected in other mafic-ultramafic complexes, especially in layered intrusions.

  4. Petrology of ultramafic and mafic xenoliths from Ruddon's Point, Fife, Scotland (United States)

    Matusiak-Malek, Magdalena; Sobczak, Paweł; Upton, Brian; Puziewicz, Jacek; Ntaflos, Theodoros


    element characteristic of peridotites, thus may represent precipitate from the metasomatic melt. Subduction-related metasomatism seems to be widespread in Scottish lithosphere south from Moine Thrust Zone, but with numerous local variations (Bonadiman et al., 2008; Hughes et al., 2015; Upton et al., 2011). The ol- clinopyroxenites and clinopyroxenites are considered to have originated by crystal settling from an alkaline silicate melt. Their formation is possibly related with Carboniferous, rifting-controlled volcanism. This study was possible thanks to project NCN UMO-2014/15/B/ST10/00095 from the Polish National Centre for Science. Bonadiman et al. (2008). Geological Society, London, Special Publication 293, 303-333 Brey, Köhler (1991). Journal of Petrology 31, 1353-1378 Hughes et al. (2015). Mineralogical Magazine, 74, 877-908 Upton et al. (2011). Journal of the Geological Society 168, 873-886

  5. Polymer layered silicate nanocomposites: Structure, morphology, and properties (United States)

    Nawani, Pranav

    Layered silicates are important fillers for improving various mechanical, flame retardant, and barrier properties of polymers, which can be attributed to their sheet-like morphology. Layered silicates can be modified with organic surfactants to render them compatible with polymer matrices. Organically modified silicates (organoclays) having large surface areas are very cost-efficient non-toxic nanofillers effective at very low loads and are readily available. Upon amalgamation of organoclays with polymer matrix nanocomposites, polymer chains can penetrate in between the silicate layers and result in an intercalated structure where the clay stack remains intact but the interlayer spacing is increased. When penetration becomes more severe, disintegration of clay stacks can occur, resulting in an exfoliated structure. It has often been observed that exfoliation is not complete down to the level of isolated silicate layers; rather, the large clay stacks are broken up into shorter stacks termed 'tactoids' together with a few individual silicate layers, resulting in a kind of mixed intercalated-exfoliated structure. Organoclay particles are mostly intercalated, having a preferred orientation with the clay gallery planes being preferentially parallel to the plane of the pressed film. Preferential orientation of organoclays affects the barrier properties of polymer membranes. Additional fillers like carbon black can induce a change in the orientation of organoclays. The effect of carbon black on the orientation of organoclays was elucidated and a relationship between orientation and permeability of air through such membranes was established. We have also investigated the flammability properties of a series of polymer nanocomposites, containing various Transition Metal Ion (TMI) modified organoclays. The improved fire retardation in nanocomposites with TMI-modified organoclays can be attributed to enhanced carbonaceous char formation during combustion, i.e., charring

  6. Leaf application of silicic acid to upland rice and corn

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    Carlos Alexandre Costa Crusciol


    Full Text Available This study aimed to evaluate the effect of Si (stabilized silicic acid, Silamol® leaf application on mineral nutrition and yield in upland rice and corn crops. The treatments were the control (without Si and Si foliar split spraying using 2 L ha-1 of the Silamol® commercial product, with 0.8% soluble Si as concentrated stabilized silicic acid. Silicon leaf application increased the concentrations of K, Ca and Si in rice and corn leaves, the number of panicles per m2 of rice and the number of grains per ear of corn; accordingly, the Si leaf application provided a higher grain yield in both crops.

  7. Geochemistry and zircon ages of mafic dikes in the South Qinling, central China: evidence for late Neoproterozoic continental rifting in the northern Yangtze block (United States)

    Zhu, Xiyan; Chen, Fukun; Liu, Bingxiang; Zhang, He; Zhai, Mingguo


    Neoproterozoic volcanic-sedimentary sequences of the southern Qinling belt, central China, were intruded by voluminous mafic dikes. secondary ion mass spectrometry zircon U-Pb dating indicates that these dikes were emplaced at 650.8 ± 5.2 Ma, coeval with mafic rocks occurring at the northern margin of the Yangtze block. The dikes are characterized by enrichment of large ion lithophile elements, high Ti contents (up to 3.73 wt%) and Nb/Ta ratios between 14.5 and 19.6, suggesting a mantle source of oceanic island basalt affinity. Initial 87Sr/86Sr ratios show positive correlation with SiO2 contents and negative correlation with Zr/Nb ratios, implying that these rocks were affected by crustal contamination during the magma ascend and emplacement process. The dikes have initial ɛ Nd values of +0.2 to +3.3, low 206Pb/204Pb ratios of 16.96-17.45, and moderate 87Sr/86Sr ratios of 0.7043-0.7076, likely pointing to the involvement of an enriched mantle source. The mafic dikes and coeval mafic volcanic equivalents in the South Qinling and the northern Yangtze are hypothesized to be related with the prolonged breakup of the supercontinent Rodinia, suggesting that continental rifting lasted until ca. 650 Ma.

  8. Non-conservative controls on distribution of dissolved silicate in Cochin Backwaters

    Digital Repository Service at National Institute of Oceanography (India)

    Balachandran, K.K.; Sankaranarayanan, V.N.; Joseph, T.; Nair, M.

    Cochin backwater system was studied with regard to dissolved silicate (DSi) to understand its seasonal distribution and behaviour during estuarine mixing. Silicate had a linear relationship with salinity during the high river discharge period...

  9. Quantitative Estimation of the Reinforcing Effect of Layered Silicates in PP Nanocomposites

    NARCIS (Netherlands)

    Szazdi, Laszlo; Pukansky Jr, Bela; Vancso, Gyula J.; Pukanszky, B.; Pukanszky, Bela


    Various polypropylene/layered silicate composites were prepared with different silicate contents. Montmorillonites with and without organophilization as well as three maleinated polypropylenes were used to change the extent of exfoliation and hence the properties of the composites. Structure was

  10. Field-trip guide to mafic volcanism of the Cascade Range in Central Oregon—A volcanic, tectonic, hydrologic, and geomorphic journey (United States)

    Deligne, Natalia I.; Mckay, Daniele; Conrey, Richard M.; Grant, Gordon E.; Johnson, Emily R.; O'Connor, Jim; Sweeney, Kristin


    The Cascade Range in central Oregon has been shaped by tectonics, volcanism, and hydrology, as well as geomorphic forces that include glaciations. As a result of the rich interplay between these forces, mafic volcanism here can have surprising manifestations, which include relatively large tephra footprints and extensive lava flows, as well as water shortages, transportation and agricultural disruption, and forest fires. Although the focus of this multidisciplinary field trip will be on mafic volcanism, we will also look at the hydrology, geomorphology, and ecology of the area, and we will examine how these elements both influence and are influenced by mafic volcanism. We will see mafic volcanic rocks at the Sand Mountain volcanic field and in the Santiam Pass area, at McKenzie Pass, and in the southern Bend region. In addition, this field trip will occur during a total solar eclipse, the first one visible in the United States in more than 25 years (and the first seen in the conterminous United States in more than 37 years).The Cascade Range is the result of subduction of the Juan de Fuca plate underneath the North American plate. This north-south-trending volcanic mountain range is immediately downwind of the Pacific Ocean, a huge source of moisture. As moisture is blown eastward from the Pacific on prevailing winds, it encounters the Cascade Range in Oregon, and the resulting orographic lift and corresponding rain shadow is one of the strongest precipitation gradients in the conterminous United States. We will see how the products of the volcanoes in the central Oregon Cascades have had a profound influence on groundwater flow and, thus, on the distribution of Pacific moisture. We will also see the influence that mafic volcanism has had on landscape evolution, vegetation development, and general hydrology.

  11. Petrogenesis of the magmatic complex at Mount Ascutney, Vermont, USA - I. Assimilation of crust by mafic magmas based on Sr and O isotopic and major element relationships (United States)

    Foland, K.A.; Henderson, C.M.B.; Gleason, J.


    The Ascutney Mountain igneous complex in eastern Vermont, USA, is composed of three principal units with compositions ranging from gabbro to granite. Sr and O isotopic and major element relationships for mafic rocks, granites, and nearby gneissic and schistose country rock have been investigated in order to describe the petrogenesis of the mafic suite which ranges from gabbro to diorite. The entire complex appears to have been formed within a short interval 122.2??1.2 m.y. ago. The granites with ??18O near +7.8??? had an initial 87Sr/86Sr of 0.70395(??6) which is indistinguishable from the initial ratio of the most primitive gabbro. Initial 87Sr/86Sr ratios and ??18O values for the mafic rocks range from 0.7039 to 0.7057 and +6.1 to +8.6???, respectively. The isotopic ratios are highly correlated with major element trends and reflect considerable crustal contamination of a mantle-derived basaltic parent magma. The likely contaminant was Precambrian gneiss similar to exposed bedrock into which the basic rocks were emplaced. A new approach to modelling of assimilation during the formation of a cogenetic igneous rock suite is illustrated. Chemical and isotopic modelling indicate that the mafic rocks were produced by simultaneous assimilation and fractional crystallization. The relative amounts of fractionation and assimilation varied considerably. The mafic suite was not produced by a single batch of magma undergoing progressive contamination; rather, the various rocks probably were derived from separate batches of magma each of which followed a separate course of evolution. The late stage granite was apparently derived from basaltic magma by fractionation with little or no crustal assimilation. The early intrusive phases are much more highly contaminated than the final one. The observed relationships have important implications for the formation of comagmatic complexes and for isotopic modelling of crustal contamination. ?? 1985 Springer-Verlag.

  12. Nd-Sr-Hf-Pb Isotopic Evidence for a Mantle Plume Origin for the Mafic Rocks from the Palaeotethyan Karakaya Complex, Turkey (United States)

    Sayit, K.; Hanan, B. B.; Göncüoglu, M.; Furman, T.


    The Karakaya Subduction/Accretion Complex consists of various pre-Liassic melange units that record the closing of the Palaeotethys ocean basin. One of these melange units, the Nilufer Unit, is composed of variably metamorphosed (dominantly prehnite-pumpellyite to greenschist facies), mafic rock assemblages that are primarily associated with neritic/pelagic limestones, mudstones and chert. The metabasic rocks are thought to represent oceanic islands/seamounts formed on the Palaeotethyan oceanic crust, fed by a mantle plume. The mafic rocks within the Nilufer Unit have mainly alkaline OIB-type geochemical signature, with marked enrichment in the most incompatible elements, relative to N-MORB. A subset of the mafic rocks are characterized by tholeiitic E-MORB-type signatures. Trace element modelling of elements least effected by metamorphism shows that the mafic rocks have been generated across a source region where garnet- and spinel-facies melts were variably mixed. The Sr isotopic values of the Nilufer mafic rocks are highly variable, indicative of post-magmatic redistribution of Sr and/or Rb. In contrast, the Nd-Hf-Pb systematics provide consistent isotope variations and source affinities in multi-isotope plots. The variations in these rocks cannot be explained solely by a single end-member or binary mixing. Instead, a multi-component mixing between three enriched sources, C-, EM II- and HIMU is required. The modelling suggests an ordered sequence of mixing initially between EM II and HIMU, followed by mixing between the C-like mantle source and the hybrid mantle. In terms of a physical model, the plume may have derived from a heterogeneous deep mantle source, or alternatively, result from the interaction of C-like plume material, upwelling from the margins of the African superplume, with continental lithosphere mantle adjacent to Palaeotethys ocean basin.


    African Journals Online (AJOL)



    Feb 29, 2012 ... Calc-silicate diffusion zones between marble and pelitic schist. Journal of. Petrology, 16, 314-346. Turner, D. C., 1983. Upper Proterozoic Schist Belts in the Nigerian sector of the Pan-African province of West Africa. Precambrian Research, 21, 55-. 79. Van de Kamp, P. C., 1968. Geochemistry and origin of.

  14. Dry phosphorus silicate glass etching for multicrystalline silicon solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Nositschka, W.A.; Voigt, O.; Kurz, H. [Aachen Univ. (Germany). Inst. of Semiconductor Electronics; Kenanoglu, A.; Borchert, D. [Fraunhofer Inst. for Solar Energy Systems, Gelsenkirchen (Germany)


    A dry plasma etching process for phosphorus silicate glass (PSG) in a SiN-PECVD batch reactor is developed. In the same reactor PSG etching and anti-reflective coating (ARC) can be performed successively. To demonstrate industrial feasibility, screen-printed solar cells are manufactured and compared with cells prepared by a standard wet chemical process. (Author)

  15. Effects of Mixed Alkaline Earth Oxides in Potash Silicate Glass ...

    African Journals Online (AJOL)

    The aim of this work is to investigate the effects of mixed alkaline earth oxide in potash silicate glasses with regards to their physical properties. More recently; there has been an increase in the demand for light weight glasses which retains their physical and chemical properties for both domestic and industrial applications.

  16. High-pressure physical properties of magnesium silicate post ...

    Indian Academy of Sciences (India)

    dLaboratory for Shock Wave and Detonation Physics Research, Institute of Fluid Physics, Academy of Engineering. Physics, PO Box 919-102, Mianyang 621900, China. MS received 1 May 2011. Abstract. The structure, thermodynamic and elastic properties of magnesium silicate (MgSiO3) post-perovskite at high pressure ...

  17. Vesuvianite–wollastonite–grossular-bearing calc-silicate rock near ...

    Indian Academy of Sciences (India)

    This paper reports the occurrence of vesuvianite + wollastonite + grossular + diopside + microcline + quartz assemblage in an enclave of calc-silicate rocks occurring within quartzofeldspathic gneiss near Tatapani in the western part of Chhotanagpur Gneissic Complex. The enclave contains phlogopite-absent and ...

  18. Effects of Aluminium–Magnesium Silicate on Newcastle Disease ...

    African Journals Online (AJOL)

    Effect of a synthetic Aluminium – Magnesium Silicate (AMS) on Newcastle Disease Virus (NDV) was tested. Equal amounts, of the AMS and of NDV, on a volume to weight (v/w) basis, were incubated for one hour at room temperature, and then centrifuged. The supernatant was tested for NDV titre. Portions of a virulent NDV ...

  19. Preparation and characterization of magnesium–aluminium–silicate ...

    Indian Academy of Sciences (India)

    A three-stage heating schedule involving calcination, nucleation and crystallization, has been evolved for the preparation of magnesium aluminium silicate (MAS) glass ceramic with MgF2 as a nucleating agent. The effect of sintering temperature on the density of compacted material was studied. Microstructure and ...

  20. Determination of reactivity rates of silicate particle-size fractions

    Directory of Open Access Journals (Sweden)

    Angélica Cristina Fernandes Deus


    Full Text Available The efficiency of sources used for soil acidity correction depends on reactivity rate (RR and neutralization power (NP, indicated by effective calcium carbonate (ECC. Few studies establish relative efficiency of reactivity (RER for silicate particle-size fractions, therefore, the RER applied for lime are used. This study aimed to evaluate the reactivity of silicate materials affected by particle size throughout incubation periods in comparison to lime, and to calculate the RER for silicate particle-size fractions. Six correction sources were evaluated: three slags from distinct origins, dolomitic and calcitic lime separated into four particle-size fractions (2, 0.84, 0.30 and <0.30-mm sieves, and wollastonite, as an additional treatment. The treatments were applied to three soils with different texture classes. The dose of neutralizing material (calcium and magnesium oxides was applied at equal quantities, and the only variation was the particle-size material. After a 90-day incubation period, the RER was calculated for each particle-size fraction, as well as the RR and ECC of each source. The neutralization of soil acidity of the same particle-size fraction for different sources showed distinct solubility and a distinct reaction between silicates and lime. The RER for slag were higher than the limits established by Brazilian legislation, indicating that the method used for limes should not be used for the slags studied here.

  1. Estimation of high temperature metal-silicate partition coefficients (United States)

    Jones, John H.; Capobianco, Christopher J.; Drake, Michael J.


    It has been known for some time that abundances of siderophile elements in the upper mantle of the Earth are far in excess of those expected from equilibrium between metal and silicate at low pressures and temperatures. Murthy (1991) has re-examined this excess of siderophile element problem by estimating liquid metal/liquid silicate partition coefficients reduces from their measured values at a lower temperature, implying that siderophile elements become much less siderophilic at high temperatures. Murthy then draws the important conclusion that metal/silicate equilibrium at high temperatures can account for the abundances of siderophile elements in the Earth's mantle. Of course, his conclusion is critically dependent on the small values of the partition coefficients he calculates. Because the numerical values of most experimentally-determined partition coefficients increase with increasing temperature at both constant oxygen fugacity and at constant redox buffer, we think it is important to try an alternative extrapolation for comparison. We have computed high temperature metal/silicate partition coefficients under a different set of assumptions and show that such long temperature extrapolations yield values which are critically dependent upon the presumed chemical behavior of the siderophile elements in the system.

  2. In vitro bioactivity and cytocompatibility of tricalcium silicate

    Indian Academy of Sciences (India)

    In vitro cytocompatible evaluation reveals that osteoblasts adhere and spread well on the Ca3SiO5 ceramics, indicating good bioactivity and cytocompatibility. Keywords. Tricalcium silicate; bioactivity; cytocompatibility; hydroxyapatite; osteoblasts. 1. Introduction. Up to now, many bioactive biomaterials, such as A/W glass.

  3. Mineralogy and trace element chemistry of the Siliceous Earth of ...

    Indian Academy of Sciences (India)

    R. Narasimhan (Krishtel eMaging) 1461 1996 Oct 15 13:05:22

    We report the presence of a 3–5 cm thick loose fragmental layer in the Siliceous Earth at Matti ka. Gol in the Barmer basin of Rajasthan. Petrographic, chemical and mineralogical study reveals the presence of abundant volcanic debris such as glass shards, agglutinates, hollow spheroids, kinked biotites, feldspars showing ...

  4. Potassium silicate-zinc oxide solution for metal finishes (United States)

    Schutt, J. B.


    Examples of zinc dust formulations, which are not subject to cracking or crazing, are fire retardant, and have high adhesive qualities, are listed. The potassium silicate in these formulations has mol ratios of dissolved silica potassium oxide in the range 4.8 to 1 - 5.3 to 1.

  5. Fluoroalkylsilane versus Alkylsilane as Hydrophobic Agents for Silica and Silicates

    Directory of Open Access Journals (Sweden)

    Damian Ambrożewicz


    Full Text Available Hydrophobic powders were obtained via surface modification of silica or magnesium silicate with selected silanes. A modified precipitation method, carried out in an emulsion system, was used for monodisperse silica synthesis, while magnesium silicate was precipitated in a traditional water system. Functionalization of the obtained inorganic supports was performed with selected alkylsilanes: one newly synthesized, 3-(2,2,3,3,4,4,5,5-octafluoropentyloxypropyltriethoxysilane (OPF, and two commercial, octadecylsilane (ODS and octyltriethoxysilane C14H32O3Si (OCS, in amounts of 3, 5, or 10 weight parts by mass of SiO2. It was determined how the chemical modification of the silica or magnesium silicate surface affected its physicochemical properties. The dispersive characteristics of both unmodified and functionalized silica-based systems were evaluated. The morphology and microstructure of the samples obtained were analyzed using scanning electron microscopy. The parameters of porous structure of the prepared systems were evaluated on the basis of BET equation as well as nitrogen adsorption/desorption isotherms. Wettability tests as well as elemental analysis of the obtained inorganic oxide hybrids were also performed. In order to verify the effectiveness of silica and magnesium silicate surface functionalization with selected silanes, FTIR spectra were investigated. The resulting experimental data allowed calculation of the degree of coverage of the silica-based systems with modifying agents.

  6. Evaluation of Calcium Silicate Cement Bond Strength after Using ...

    African Journals Online (AJOL)


    Jan 24, 2018 ... Objectives: To determine the effect of different gutta‑percha solvents. (chloroform, Endosolv E, orange oil, and eucalyptol) on the push‑out bond strength of calcium silicate cements (CSCs; white mineral trioxide aggregate. [WMTA]; capsule‑form mineral trioxide aggregate [CMTA], and Biodentine). Materials ...

  7. Energetics of silicate melts from thermal diffusion studies

    Energy Technology Data Exchange (ETDEWEB)

    Walker, D.


    Efforts are reported in the following areas: laboratory equipment (multianvils for high P/T work, pressure media, SERC/DL sychrotron), liquid-state thermal diffusion (silicate liquids, O isotopic fractionation, volatiles, tektites, polymetallic sulfide liquids, carbonate liquids, aqueous sulfate solutions), and liquid-state isothermal diffusion (self-diffusion, basalt-rhyolite interdiffusion, selective contamination, chemical diffusion).

  8. 77 FR 21676 - Silicic Acid, Sodium Salt etc.; Tolerance Exemption (United States)


    ... chlorotrimethylsilane and iso-propyl alcohol, reaction with poly(oxypropylene)-poly(oxyethylene) glycol; when used as an... residues of Silicic acid, sodium salt, reaction products with chlorotrimethylsilane and iso-propyl alcohol...-OPP-2011-0934, by one of the following methods. Federal eRulemaking Portal:

  9. Ubiquitous high-FeO silicates in enstatite chondrites (United States)

    Lusby, David; Scott, Edward R. D.; Keil, Klaus


    SEM and EMPA were used to determine the mineral contents of four EH3 chondrites. All four showed the dominant enstatite peak, Fs 0-5, with 4-8 percent of FeO-rich pyroxene with Fs 5-20. Among the 542 objects found to contain high-FeO silicates, 18 were chondrules, 381 were rimmed or unrimmed grains, and 143 were aggregates. The high-FeO silicates in these objects are very largely pyroxene with Fs 5-23. Large grains of both FeO-rich and FeO-poor silicates were found to be present in the FeO-rich chondrules. This fact, together with the absence of clasts of FeO-rich chondritic material in the EH3 chondrites, suggests that FeO-rich grains were introduced before or during chondrule formation. It is concluded that FeO-rich and FeO-poor silicates were both present in the nebular region where E chondrites originated.

  10. Mineralogy and trace element chemistry of the Siliceous Earth of ...

    Indian Academy of Sciences (India)

    We report the presence of a 3-5 cm thick loose fragmental layer in the Siliceous Earth at Matti ka Gol in the Barmer basin of Rajasthan. Petrographic, chemical and mineralogical study reveals the presence of abundant volcanic debris such as glass shards, agglutinates, hollow spheroids, kinked biotites, feldspars showing ...

  11. Oxygen from the lunar soil by molten silicate electrolysis (United States)

    Colson, Russell O.; Haskin, Larry A.


    Accepting that oxygen, rather than gigantic gems or gold, is likely to make the Moon's Klondike, the extraction of oxygen from the lunar soil by molten silicate electrolysis has chosen to be investigated. Process theory and proposed lunar factory are addressed.

  12. A Siliceous Microfossil View of Middle Eocene Arctic Paleoenvironments (United States)

    Stickley, C. E.; Koc, N.; Brumsack, H.; Jordan, R. W.; Suto, I.


    Integrated Ocean Drilling Program Expedition 302, "The Arctic Coring Expedition" (ACEX) made arguably the most significant discovery of Paleogene siliceous microfossils in nearly 2 decades. 100 m of mm to sub-mm laminated biosiliceous sediments of Middle Eocene age are rich in marine and freshwater siliceous microfossils allowing intriguing insights into central Arctic paleoenvironments during the start of Cenozoic cooling to icehouse conditions. Largely endemic assemblages of marine diatoms and ebridians are preserved along with very high abundances of chrysophyte cysts, the endogenously formed resting stage of freshwater algae. These siliceous microfossil groups imply an overall brackish environment, but variations in group dominance suggest episodic variations in salinity, stratification and trophic status. We synthesize the overall characteristics of the biosiliceous sediments by reporting on broad scale variations in siliceous microfossils and give some exciting insights into the composition of the laminae which may help explain the formation of these sediments. Our results indicate basin-wide paleo-environmental fluctuations on long- and possibly seasonal timescales.

  13. Mesoporous silicates: Materials science and biological applications (United States)

    Roggers, Robert Anthony

    This thesis dissertation presents the collective research into the advancement of mesoporous silicate particles as biointerface devices, the development of new materials and the application of these particles as solid supports for heterogeneous catalysis. Mesoporous silica has been utilized in the aforementioned applications due to several reasons; the first being the ability to achieve high surface areas (500 - 1000 m2 g-1) with controlled pore sizes and particle morphology. Another reason for their popularity is their robustness in applications of heterogeneous catalysis and the ability to functionalize the surface with a wide variety of organic functional groups. In the field of biointerface devices, mesoporous silica nanoparticles represent a class of materials that exhibit high biocompatibility. In addition, the ability to functionalize the surfaces (outer surface and pore interiors) allows the particles to be targeted to specific cell types as well as the ability to release many different therapeutic molecules under specific stimuli. A unique particle coating consisting of a chemically cleavable lipid bilayer that allows for the encapsulation of a fluorescent molecule and increases the biocompatibility of the particle has been developed. The lipid bilayer coated mesoporous silica nanoparticle (LB-MSN) was characterized using X-ray diffraction, transmission electron microscopy and nitrogen `sorption isotherms. The finished LB-MSN was then incubated with mammalian cells in order to prove their biocompatibility. Confocal micrographs demonstrate the endocytosis of the particles into the cells. In addition the micrographs also show that the LB-MSNs are separate from the endosomal compartments, however due to the lipophilic nature of the dye used to label the endosome there is some debate regarding this conclusion. The lipid bilayer coating was then applied to a large pore MSN (l-MSN) which had been previously shown to cause lysis of red blood cells (RBCs) at low

  14. Silicate Dispersion and Mechanical Reinforcement in Polysiloxane/Layered Silicate Nanocomposites

    KAUST Repository

    Schmidt, Daniel F.


    We report the first in-depth comparison of the mechanical properties and equilibrium solvent uptake of a range of polysiloxane nanocomposites based on treated and untreated montmorillonite and fumed silica nanofillers. We demonstrate the ability of equilibrium solvent uptake data (and, thus, overall physical and chemical cross-link density) to serve as a proxy for modulus (combining rubber elasticity and Flory-Rehner theory), hardness (via the theory of Boussinesq), and elongation at break, despite the nonideal nature of these networks. In contrast, we find that tensile and tear strength are not well-correlated with solvent uptake. Interfacial strength seems to dominate equilibrium solvent uptake and the mechanical properties it predicts. In the montmorillonite systems in particular, this results in the surprising consequence that equilibrium solvent uptake and mechanical properties are independent of dispersion state. We conclude that edge interactions play a more significant role than degree of exfoliation, a result unique in the field of polymer nanocomposites. This demonstrates that even a combination of polymer/nanofiller compatibility and thermodynamically stable nanofiller dispersion levels may not give rise to reinforcement. These findings provide an important caveat when attempting to connect structure and properties in polymer nanocomposites, and useful guidance in the design of optimized polymer/layered silicate nanocomposites in particular. © 2009 American Chemical Society.

  15. Production test IP-728 half-plant sodium silicate test. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Geier, R.G.


    The sodium silicate addition to the coolant reduced the effluent concentrations of certain radionuclides. Nothing was observed during the course of the test to indicate that sodium silicate could not be used at all plants. However, the reductions obtained in effluent activity are not believed commensurate with the cost of silicate usage.

  16. Silicate Phases on the Surfaces of Trojan Asteroids (United States)

    Martin, Audrey; Emery, Joshua P.; Lindsay, Sean S.


    Determining the origin of asteroids provides an effective means of constraining the solar system’s dynamic past. Jupiter Trojan asteroids (hereafter Trojans) may help in determining the amount of radial mixing that occurred during giant planet migration. Previous studies aimed at characterizing surface composition show that Trojans have low albedo surfaces and are spectrally featureless in the near infrared. The thermal infrared (TIR) wavelength range has advantages for detecting silicates on low albedo asteroids such as Trojans. The 10 μm region exhibits strong features due to the Si-O fundamental molecular vibrations. Silicates that formed in the inner solar system likely underwent thermal annealing, and thus are crystalline, whereas silicates that accreted in the outer solar system experienced less thermal processing, and therefore are more likely to have remained in an amorphous phase. We hypothesize that the Trojans formed in the outer solar system (i.e., the Kuiper Belt), and therefore will have a more dominant amorphous spectral silicate component. With TIR spectra from the Spitzer Space Telescope, we identify mineralogical features from the surface of 11 Trojan asteroids. Fine-grain mixtures of crystalline pyroxene and olivine exhibit a 10 μm feature with sharp cutoffs between about 9 μm and 12 μm, which create a broad flat plateau. Amorphous phases, when present, smooth the sharp emission features, resulting in a dome-like shape. Preliminary results indicate that the surfaces of analyzed Trojans contain primarily amorphous silicates. Emissivity spectra of asteroids 1986 WD and 4709 Ennomos include small peaks in the 10 μm region, diagnostic of small amounts of crystalline olivine. One explanation is that Trojans formed in the same region as Kuiper Belt objects, and when giant planet migration ensued, they were swept into Jupiter’s stable Lagrange points where they are found today. As such, it is possible that an ancestral group of Kuiper Belt

  17. Wastewater reuse in liquid sodium silicate manufacturing in alexandria, egypt. (United States)

    Ismail, Gaber A; Abd El-Salam, Magda M; Arafa, Anwar K


    Soluble sodium silicates (waterglass) are liquids containing dissolved glass which have some water like properties. They are widely used in industry as sealants, binders, deflocculants, emulsifiers and buffers. Their most common applications in Egypt are in the pulp and paper industry (where they improve the brightness and efficiency of peroxide bleaching) and the detergent industry, in which they improve the action of the detergent and lower the viscosity of liquid soaps. The survey results showed that the production was carried out batch-wise, in an autoclave (dissolver). Sodium silicate in the state of crushed glass was charged in an autoclave (dissolver) with sodium hydroxide and water. The product is filtered through a press. The left over sludge (mud and silicates impurities) is emptied into the local sewer system. Also, sludge (silica gel) was discharged from the neutralization process of the generated alkaline wastewater and consequently clogging the sewerage system. So this study was carried out to modify the current wastewater management system which eliminates sludge formation, the discharge of higher pH wastewater to the sewer system, and to assess its environmental and economic benefits. To assess the characteristics of wastewater to be reused, physico-chemical parameters of 12 samples were tested using standard methods. The survey results showed that a total capacity of the selected enterprise was 540 tons of liquid sodium silicates monthly. The total amount of wastewater being discharged was 335 m3/month. Reusing of wastewater as feed autoclave water reduced water consumption of 32.1% and reduced wastewater discharge/month that constitutes 89.6% as well as saving in final product of 6 ton/month. It was concluded that reusing of wastewater generated from liquid sodium silicate manufacturing process resulted in cheaper and environmental-friendly product.

  18. Effect of silicate module of water glass on rheological parameters of poly(sodium acrylate)/sodium silicate hydrogels (United States)

    Mastalska-Popiawska, J.; Izak, P.


    The poly(sodium acrylate)/sodium silicate hydrogels were synthesized in the presence of sodium thiosulphate and potassium persulphate as the redox initiators and N,N’-methylene-bisacrylamide as the cross-linking monomer. 20 wt% aqueous solution of sodium acrylate was polymerized together with water glass with different silicate modules (M) from 1.74 to 2.29, in three mass ratio of the monomer solution to the water glass 2:1, 1:1 and 1:2. Such obtained hybrid composites were rheologically tested using the oscillation method. It allowed to designate the crossover point during polymerization, as well as to define the viscoelastic properties of the casted hydrogel samples one week after the reaction. The obtained results of the oscillation measurements showed that cross-linking reaction proceeds very quickly and the lower the silicate module is, the process starts faster. After the completion of the reaction the silicate-polymer hydrogels are strongly elastic materials and the highest elasticity characterizes systems with the mass ratio 1:2, i.e. with the highest water glass content.

  19. Mafic dyke swarms of the Bastar Craton, central India: geochemistry, Sr-Nd isotopes and tectonic implications (United States)

    Liao, Chien-Yi; Shellnutt, J. Gregory; Raghvan Hari, Kosiyathu; Viswakarma, Neeraj


    The Archean Bastar Craton of central India which is demarcated by Godivari rift in the west, Mahanadi rift in the east, Narmada-Son rift in the north and the Eastern Ghats Mobile Belt in the south was intruded by several generations of mafic dyke swarms during the Precambrian, with most of the dykes NW-SE to WNW-ESE trending. The dyke swarms can be subdivided into three main groups: the Meso-Neoarchean sub-alkaline mafic dykes (BD1), Neoarchean to Paleoproterozoic boninite-norite dykes (BN) and Paleoproterozoic sub-alkaline mafic dykes (BD2). In the present work, an attempt has been made to constrain the petrogenesis and tectonic implications of the dykes in the Bhanupratapur area of central Bastar Craton. Petrographically, the dykes are metabasites / metadolerites that experienced hydrothermal alteration, as most of the samples are moderately to highly altered. Primary minerals were replaced but still retain the original igneous texture (ophitic). The least-altered samples contain orthopyroxene, plagioclase, secondary amphibole, secondary quartz and some euhedral Fe-Ti oxides. The dykes can be classified into two groups according to major element data. Petrographically, the two groups cannot be clearly distinguished. Group 1 is sub-alkaline basalt (SiO2 = 51 wt%) with low magnesium (MgO = 4.6 to 7.2 wt%), low Mg-number (Mg# ≤ 53) and higher titanium (TiO2 ≥ 0.83 wt%). Group 2 is sub-alkaline basaltic andesite and has boninitic characteristics with higher silica (SiO2 = 51 to 56 wt%), higher magnesium (MgO = 5.9 to 19.1 wt%), higher Mg-number (Mg# = 50 to 79) and lower titanium (TiO2 ≤ 0.8 wt%). The chondrite-normalized REE patterns of Group 1 show variability in the light rare earth elements (La/SmN = 1.2 to 2.4). Group 2 exhibit light rare earth element enrichment (La/YbN = 2.2 to 10.4). The Sm-Nd isochron age of Group 1 is approximately 1.9 Ga, with the initial 87Sr/86Sr ratios range from 0.7029 to 0.7058 and ɛNd(t) values range from-0.9 to +1.8. Group 1

  20. Biological and therapeutic effects of ortho-silicic acid and some ortho-silicic acid-releasing compounds: New perspectives for therapy

    Directory of Open Access Journals (Sweden)

    Jurkić Lela Munjas


    Full Text Available Abstract Silicon (Si is the most abundant element present in the Earth's crust besides oxygen. However, the exact biological roles of silicon remain unknown. Moreover, the ortho-silicic acid (H4SiO4, as a major form of bioavailable silicon for both humans and animals, has not been given adequate attention so far. Silicon has already been associated with bone mineralization, collagen synthesis, skin, hair and nails health atherosclerosis, Alzheimer disease, immune system enhancement, and with some other disorders or pharmacological effects. Beside the ortho-silicic acid and its stabilized formulations such as choline chloride-stabilized ortho-silicic acid and sodium or potassium silicates (e.g. M2SiO3; M= Na,K, the most important sources that release ortho-silicic acid as a bioavailable form of silicon are: colloidal silicic acid (hydrated silica gel, silica gel (amorphous silicon dioxide, and zeolites. Although all these compounds are characterized by substantial water insolubility, they release small, but significant, equilibrium concentration of ortho-silicic acid (H4SiO4 in contact with water and physiological fluids. Even though certain pharmacological effects of these compounds might be attributed to specific structural characteristics that result in profound adsorption and absorption properties, they all exhibit similar pharmacological profiles readily comparable to ortho-silicic acid effects. The most unusual ortho-silicic acid-releasing agents are certain types of zeolites, a class of aluminosilicates with well described ion(cation-exchange properties. Numerous biological activities of some types of zeolites documented so far might probably be attributable to the ortho-silicic acid-releasing property. In this review, we therefore discuss biological and potential therapeutic effects of ortho-silicic acid and ortho-silicic acid -releasing silicon compounds as its major natural sources.

  1. Plagioclase crystal size distribution in some tholeiitic mafic dykes in Cabo Frio-Buzios, Rio de Janeiro, Brazil (United States)

    Ngonge, E. Donald; Archanjo, C. J.; Hollanda, M. H. B. M.


    Crystal size distribution (CSD) has been constrained in plagioclase in two mafic dykes of the Conchas Beach and one at the Lagoinha Beach in the Cabo Frio-Buzios NE-trending dyke swarm. At contact with the metamorphic basement the texture is fine-grained and microporphyritic and intergranular at the center of the larger dykes. Samples were collected at the margins and at the center of the dykes. The plagioclase average characteristic size (C) varies from 0.07 to 0.13 mm at the margins of the narrow dykes and from 0.09 to 0.20 mm at the margins of the larger dyke. At the center of the Lagoinha and Conchas dykes C varies from 0.19 ± 0.02 mm and 0.60 ± 0.07 mm respectively. The CSDs at the dyke margins are concave-up. At the center of the larger Conchas dyke (8.2 m), the CSD is log-linear, consistent with simple steady-state crystallization pattern. From the mineralogy the plagioclase phenocrysts have a high An content (bytownite-labradorite) than the groundmass grains (labradorite-andesine). At the margins olivine is richer in Fo than at the center, and respectively, pyroxene is richer in Ca. These results indicate that the chilled margin is more mafic than the center suggesting a normal chemical evolution in a cooling magma that ascended upward from depths by Newtonian to pseudoplastic flow. The concave-up CSDs probably depict heterogeneous crystallization rates possibly induced by depressurization during the magma ascent followed by rapid cooling. The log-linear CSD pattern at the center of the Conchas dyke (8.2 m width) is attributed to a higher residence time of the magma which favors the processes of chemical diffusion and textural re-equilibration. From the calculated cooling rates the larger Conchas dyke (8.2 m in width) would be completely crystallized (at ~ 900 °C) in about 2 years.

  2. Solution-mass transfer and grain boundary sliding in mafic shear zones - comparison between experiments and nature (United States)

    Marti, Sina; Heilbronner, Renée; Stünitz, Holger; Plümper, Oliver; Drury, Martyn


    Grain size sensitive creep (GSSC) mechanisms are widely recognized to be the most efficient deformation mechanisms in shear zones. With or without initial fracturing and fluid infiltration, the onset of heterogeneous nucleation leading to strong grain size reduction is a frequently described process for the initiation of GSSC. Phase mixing due to reaction and heterogeneous nucleation during GSSC impedes grain growth, sustaining small grain sizes as a prerequisite for GSSC. Here we present rock deformation experiments on 'wet' plagioclase - pyroxene mixtures at T=800°C, P=1.0 and 1.5GPa and strain rates of 2e-5 - 2e-6 1/s, performed with a Griggs-type solid medium deformation apparatus. Microstructural criteria are used to show that both, grain boundary sliding (GBS) and solution-mass transfer processes are active and are interpreted to be the dominant strain accommodating processes. Displacement is localized within shear bands formed by fine-grained ( 300 - 500nm) plagioclase (Pl) and the syn-kinematic reaction products amphibole (Amph), quartz (Qz) and zoisite (Zo). We compare our experiments with a natural case - a sheared mafic pegmatite (P-T during deformation 0.7 - 0.9 GPa, 610 - 710 °C; Getsinger et al., 2013) from Northern Norway. Except for the difference in grain size of the experimental and natural samples, microstructures are strikingly alike. The experimental and natural P- and especially T-conditions are very similar. Consequently, extrapolation from experiments to nature must be made without a significant 'temperature-time' trade-off, which is normally taken advantage of when relating experimental to natural strain rates. We will discuss under which assumptions extrapolation to nature in our case is likely feasible. Syn-kinematic reactions during GBS and solution-mass transport are commonly interpreted to result in an ordered (anticlustered) phase mixture. However, phase mixing in our case is restricted: Mixing is extensive between Pl + Zo + Qz and

  3. Dating coeval mafic magmatism and ultrahigh temperature metamorphism in the Anápolis-Itauçu Complex, Central Brazil (United States)

    Giustina, Maria Emilia Schutesky Della; Pimentel, Márcio Martins; Ferreira Filho, Cesar Fonseca; de Hollanda, Maria Helena Bezerra Maia


    Dating granulites has always been of great interest because they represent one of the most extreme settings of an orogen. Owing to the resilience of zircon, even in such severe environments, the link between P-T conditions and geological time is possible. However, a challenge to geochronologists is to define whether the growth of new zircon is related to pre- or post-P-T peak conditions and which processes might affect the (re)crystallization. In this context, the Anápolis-Itauçu Complex, a high-grade complex in central Brazil with ultrahigh temperature (UHT) granulites, may provide valuable information within this topic. The Anápolis-Itauçu Complex (AIC) includes ortho- and paragranulites, locally presenting UHT mineral assemblages, with igneous zircon ages varying between 760 and 650 Ma and metamorphic overgrowths dated at around 650-640 Ma. Also common in the Anápolis-Itauçu Complex are layered mafic-ultramafic complexes metamorphosed under high-grade conditions. This article presents the first geological and geochronological constraints of three of these layered complexes within the AIC, the Damolândia, Taquaral and Goianira-Trindade complexes. U-Pb (LA-MC-ICPMS, SHRIMP and ID-TIMS) zircon analyses reveal a spread of concordant ages spanning within an age interval of ~ 80 Ma with an “upper” intercept age of ~ 670 Ma. Under cathodoluminescence imaging, these crystals show partially preserved primary sector zoning, as well as internal textures typical of alteration during high-grade metamorphism, such as inward-moving boundaries. Zircon grains reveal homogeneous initial 176Hf/177Hf values in distinct crystal-scale domains in all samples. Moreover, Hf isotopic ratios show correlation neither with U-Pb ages nor with Th/U ratios, suggesting that zircon grains crystallized during a single growth event. It is suggested, therefore, that the observed spread of concordant U-Pb ages may be related to a memory effect due to coupled dissolution

  4. Geological setting, emplacement mechanism and igneous evolution of the Atchiza mafic-ultramafic layered suite in north-west Mozambique (United States)

    Ibraimo, Daniel Luis; Larsen, Rune B.


    The Atchiza mafic and ultramafic-layered suite (hereafter, "Atchiza Suite) crops out in an area 330 km2 west of the Mozambican Tete province. In an early account of the geology of this intrusion, it was considered the continuation of the Great Dyke of Zimbabwe, an idea that was aborted after detailed studies. Nevertheless, the Ni concentrations in the Atchiza outcrop rocks are considerable. Our investigation used field evidence, hand specimens and petrography descriptions, mineral chemistry studies using electron microprobe analysis and tectonic analysis to arrive at a plausible mineralogical composition and understanding of the tectonic setting for the igneous evolution. The mineral composition from the Atchiza Suite indicates that these are cumulates. The magmatic segregation from the petrographic and mineral composition reasoning indicates that dunite-lherzolitic peridotite-olivine gabbro-gabbronorite-gabbro-pegmatitic gabbro is the rock formation sequence. Olivine and chromite were the first phases formed, followed by pyroxene and plagioclase. In addition, it is shown that these minerals are near-liquidus crystallization products of basaltic magma with olivine Fo: 87.06 in dunite, mean values of clinopyroxene are (Wo: 36.4, En: 48.0, Fs: 15.2), orthopyroxene (Wo: 2.95, En: 73.0, Fs: 24.2) and plagioclase An: 71.3, respectively. Opaque minerals comprise Fe-Ti oxides and (Fe, Cr) spinel up to 4.8 vol.%, but chromitite layers are not present. Most of the opaque minerals are interstitial to pyroxene. Sulphides are common in gabbros, with pyrrhotite, pentlandite, chalcopyrite, pyrite and covellite together comprising 0.4-2.0 vol.%. The whole rock Rare Earth Element (REE) concentrations are mainly a result of differentiation, but slight crustal contamination/assimilation contributed to the REE contents. In addition, they also show Eu enrichment, suggesting that plagioclase fractionation was important in the rock. The Atchiza Suite preserves a deep-seated plumbing

  5. A model of sulphur solubility for hydrous mafic melts: application to the determination of magmatic fluid compositions of Italian volcanoes


    Pichavant, M.; Scaillet, B.


    We present an empirical model of sulphur solubility that allows us to calculate f S2 if P, T, fO2 and the melt composition, including H2O and S, are known. The model is calibrated against three main experimental data bases consisting in both dry and hydrous silicate melts. Its prime goal is to calculate the f S2 of hydrous basalts that currently lack experimental constraints of their sulphur solubility behaviour. Application of the model to Stromboli, Vesuvius, Vulcano and...

  6. Decoupling of the Assimilation and Fractionation Signatures in a MASH Zone: Evidence from the Sierra Valle Fértil Mafic Zone, Argentina (United States)

    Walker, B. A., Jr.; Bergantz, G. W.; Otamendi, J.; Ducea, M. N.; Cristofolini, E.


    The Sierra Valle Fértil (SVF) in northern Argentina is a tilted Ordovician fossil arc complex with continuous exposure from paleodepths of ~10 km to ~30 km. The system is layered when viewed at a large scale: shallow, granodiorite plutons give way to a heterogeneous granodiorite-tonalite zone, which in turn grades into a gabbro-tonalite zone at the base of the section. A metapelitic country rock package is interlayered throughout the magmatic complex, allowing for determination of emplacement depths within the section. Our work focuses on the lowermost domain of the SVF, as it preserves what we consider to be a frozen example of a MASH zone. Here, dominant rock types are hornblende gabbronorite and tonalitie variants, which appear to be interfingered as dm- to 10s of m-scale sheets. Mappable ultramafic pods containing dunites, websterites, troctolites, and minor anorthosites are also present. Field relations are consistent with a complex series of intrusive events. Much of the SVF mafic zone compositional array can be modeled by fractional crystallization where the mafic rocks are cumulate assemblages and the intermediate rocks are the daughter magmas. Amphibole and, perhaps more importantly, Fe-Ti oxide crystallization are likely the principal agents of silica enrichment. Metapelitic rocks exposed throughout the SVF are likely the vestiges of a country rock package that was melted (or reacted) and incorporated into SVF magmas, but field and compositional evidence for assimilation is cryptic in the mafic zone. While isotopic data (Sr, Nd, O) seem to implicate crustal contributions to the SVF mafic zone, incompatible major and trace elements typically associated with an "assimilation signature" (e.g., K, Rb, Ba) are sparse. Such elements are abundant in the metapelites and in igneous rocks farther up section. We interpret this isotopic and elemental decoupling as a byproduct of prolonged MASH processes in the lower crust. A high temperature and an increasingly

  7. Fluid Inclusion Study of Quartz Xenocrysts in Mafic Dykes from Kawant Area, Chhota Udaipur District, Gujarat, India

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    Randive Kirtikumar


    Full Text Available Unusual mafic dykes occur in the proximity of the Ambadongar Carbonatite Complex, Lower Narmada Valley, Gujarat, India. The dykes contain dense population of quartz xenocrysts within the basaltic matrix metasomatised by carbonate-rich fluids. Plagioclase feldspars, relict pyroxenes, chlorite, barite, rutile, magnetite, Fe-Ti oxides and glass were identified in the basaltic matrix. Quartz xenocrysts occur in various shapes and sizes and form an intricate growth pattern with carbonates. The xenocrysts are fractured and contain several types of primary and secondary, single phase and two-phase fluid inclusions. The two-phase inclusions are dominated by aqueous liquid, whereas the monophase inclusions are composed of carbonic gas and the aqueous inclusions homogenize to liquid between 226°C and 361°C. Majority of the inclusions are secondary in origin and are therefore unrelated to the crystallization of quartz. Moreover, the inclusions have mixed carbonic-aqueous compositions that inhibit their direct correlation with the crustal or mantle fluids. The composition of dilute CO2-rich fluids observed in the quartz xenocrysts appear similar to those exsolved during the final stages of evolution of the Amba Dongar carbonatites. However, the carbonates are devoid of fluid inclusions and therefore their genetic relation with the quartz xenocrysts cannot be established.

  8. Fluid Inclusion Study of Quartz Xenocrysts in Mafic Dykes from Kawant Area, Chhota Udaipur District, Gujarat, India (United States)

    Randive, Kirtikumar; Hurai, Vratislav


    Unusual mafic dykes occur in the proximity of the Ambadongar Carbonatite Complex, Lower Narmada Valley, Gujarat, India. The dykes contain dense population of quartz xenocrysts within the basaltic matrix metasomatised by carbonate-rich fluids. Plagioclase feldspars, relict pyroxenes, chlorite, barite, rutile, magnetite, Fe-Ti oxides and glass were identified in the basaltic matrix. Quartz xenocrysts occur in various shapes and sizes and form an intricate growth pattern with carbonates. The xenocrysts are fractured and contain several types of primary and secondary, single phase and two-phase fluid inclusions. The two-phase inclusions are dominated by aqueous liquid, whereas the monophase inclusions are composed of carbonic gas and the aqueous inclusions homogenize to liquid between 226°C and 361°C. Majority of the inclusions are secondary in origin and are therefore unrelated to the crystallization of quartz. Moreover, the inclusions have mixed carbonic-aqueous compositions that inhibit their direct correlation with the crustal or mantle fluids. The composition of dilute CO2-rich fluids observed in the quartz xenocrysts appear similar to those exsolved during the final stages of evolution of the Amba Dongar carbonatites. However, the carbonates are devoid of fluid inclusions and therefore their genetic relation with the quartz xenocrysts cannot be established.

  9. Modeling the viscosity of silicate melts containing manganese oxide

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    Kim Wan-Yi


    Full Text Available Our recently developed model for the viscosity of silicate melts is applied to describe and predict the viscosities of oxide melts containing manganese oxide. The model requires three pairs of adjustable parameters that describe the viscosities in three systems: pure MnO, MnO-SiO2 and MnO-Al2O3-SiO2. The viscosity of other ternary and multicomponent silicate melts containing MnO is then predicted by the model without any additional adjustable model parameters. Experimental viscosity data are reviewed for melts formed by MnO with SiO2, Al2O3, CaO, MgO, PbO, Na2O and K2O. The deviation of the available experimental data from the viscosities predicted by the model is shown to be within experimental error limits.

  10. Thermochemistry of Rare Earth Silicates for Environmental Barrier Coatings (United States)

    Costa, Gustavo; Jacobson, Nathan


    Rare earth silicates are promising candidates as environmental protective coatings (EBCs) for silica-forming ceramics and composites in combustion environments since they are predicted to have lower reactivity with the water vapor combustion products. The reactivity of rare earth silicates is assessed by the thermodynamic activity of the silica component which is best measured by Knudsen effusion mass spectrometry (KEMS). Here, we discuss a novel method based on a reducing agent to increase the partial pressure of SiO(g) which is then used to calculate thermodynamic activity of silica in Y2O3-SiO2 and Yb2O3-SiO2 systems. After the KEMS measurements, samples were probed by X-ray diffraction and their phase content was calculated from Rietveld refinement.

  11. The viscosity window of the silicate glass foam production

    DEFF Research Database (Denmark)

    Petersen, Rasmus Rosenlund; König, Jakob; Yue, Yuanzheng


    The production of silicate glass foam allows diverse resources and waste materials to be used in the production. Testing of such large palette of materials complicates and prolongs the optimisation process. Therefore, it is crucial to find a universal criterion for foaming silicate glass melts...... which can offer a practical starting point for the optimisation procedure. The melt viscosity might be the most important parameter for controlling the foaming process and the glass foam density. In this work, we attempt to define a viscosity range in which foaming of different glasses results...... in a maximum of foam expansion. The expansion maximum is obtained for different glasses (labware, E-glass, CRT panel, soda-lime-silica) by foaming with CaCO3 at isokom temperature and from literature data. In general, the viscosity window was found to be within 104–106 Pa s when foaming with MnO2 or metal...

  12. Participation of bacteria in weathering processes of silicates

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    Peter Javorský


    Full Text Available Biological processes presented by the metabolic activity of different species of bacteria adhered at the mineral surfaces are a part of the geochemical processes. These bacteria accelerate, by the production of organic acids into the minerals structural bonds, the leaching of elements and their subsequent and gradual transformation to the secondary minerals. Microbial destructions of silicates are studied in order to processing low-quality mineral raw-materials and the remediation of soils, sediments and waters contaminated by industrial pollutants. The samples of material, used in our research, were obtained at 9 deposits of non-metallic raw-materials in Slovakia. The sediment sample was taken from the area of Baikal Lake. The presence of microorganisms in the matrix most frequently was determined by a subsequent isolation of microorganisms and identification of bacterial species presented in the silicate matrix. The species of Bacillus and Pseudomonas genus were the common representative of the microorganisms.

  13. Enzyme-Mimicking properties of silicates and other minerals (United States)

    Siegel, B. Z.; Siegel, S. M.

    The adsorptive and/or catalytic properties of clays, silicates in general, and other minerals are well known. More recently, their probable role in prebiotic syntheses of bio-organic compounds has become a matter of record. We demonstrate that, in addition to their role in de novo formation of important biomolecules, clays, micas, fibrous silicates and other minerals mimick the activities of contemporary enzymes including oxidases, esterases, phosphatases and glucosidases. The existence of such capabilities in substances likely to be represented on the surfaces of Earth-like planets may offer a challenge to the technology and design of remote life detection systems which must then distinguish between bona fide biological chemistry and mineral-base pseudometabolism. It also raises questions about the importance of mineral surfaces in post-mortem transformations of organic metabolites in our own biosphere.

  14. The solubility of gold in silicate melts: First results (United States)

    Borisov, A.; Palme, H.; Spettel, B.


    The effects of oxygen fugacity and temperature on the solubility of Au in silicate melts were determined. Pd-Au alloys were equilibrated with silicate of anorthite-diopside eutectic composition at different T-fO2 conditions. The behavior of Au was found to be similar to that of Pd reported recently. Au solubilities for alloys with 30 to 40 at. percent Au decrease at 1400 C from 12 ppm in air to 160 ppb at a log fO2 = -8.7. The slope of the log(Me-solubility) vs. log(fO2) curve is close to 1/4 for Au and the simultaneously determined Pd suggesting a formal valence of Au and Pd of 1+. Near the IW buffer Pd and Au solubilities become even less dependent on fO2 perhaps reflecting the presence of some metallic Au and Pd.

  15. Conductivity studies of lithium zinc silicate glasses with varying ...

    Indian Academy of Sciences (India)


    biomedical applications (McMillan 1979). The lithium– zinc–silicate (LZS) glass containing Li2O–ZnO–SiO2–. Na2O–B2O3–P2O5 has been used as the base glass for producing glass ceramics that are suitable for applications in hermetic glass–ceramic–to–metal seals with a variety of metals and alloys (Sharma et al 2004) ...

  16. Cracking phenomena in lithium-di-silicate glass ceramics

    Indian Academy of Sciences (India)


    Abstract. Lithium-di-silicate glass ceramic (Li2O, SiO2) with uniformly oriented crystals was placed on a. Vickers indentation with extrusion axis horizontally parallel to the base axis. The material was rotated through. 0°– 90° and at each angle a 20 N load was applied to ascertain the crack path. It was observed that the crack.

  17. Cracking phenomena in lithium-di-silicate glass ceramics

    Indian Academy of Sciences (India)

    Lithium-di-silicate glass ceramic (Li2O, SiO2) with uniformly oriented crystals was placed on a Vickers indentation with extrusion axis horizontally parallel to the base axis. The material was rotated through 0°– 90° and at each angle a 20 N load was applied to ascertain the crack path. It was observed that the crack length ...

  18. Apatite: a new redox proxy for silicic magmas?


    Miles, A.J.; Graham, C M; Hawkesworth, C.J.; Gillespie, M.R.; Hinton, R.W.; Bromiley, G.D.


    The oxidation states of magmas provide valuable information about the release and speciation of volatile elements during volcanic eruptions, metallogenesis, source rock compositions, open system magmatic processes, tectonic settings and potentially titanium (Ti) activity in chemical systems used for Ti-dependent geothermometers and geobarometers. In this paper we explore the use of Mn in apatite as an oxybarometer in intermediate and silicic igneous rocks. Increased Mn concentrations in apati...


    Directory of Open Access Journals (Sweden)

    V. A. Aseev


    Full Text Available We created and synthesized luminescent composite of the "phosphor in glass" type, based on the lead-silicate matrix and fine-dispersed powder of cerium-activated yttrium-aluminum garnet crystal. Lead-silicate system (40SiO2- 20PbO-(40-x PbF2-xAlF3, x = 0-25 was chosen as the glassy matrix. Initial glass was reduced to powder (frit for "phosphor in glass" composite with a particle size about 50 µm. Glass frit and powder of commercial YAG:Ce3+ phosphor were mixed in a ratio of 30 to 70 (wt %. Then this composite was pressed in a tablet and sintered on a quartz substrate at 823 К for 30 minutes. Thus, the plane parallel sheet for composite of the "phosphor in glass" was obtained with a diameter equal to 10 mm. For the purpose to reduce the loss of light in the presence of dispersion at a glass-phosphor boundary, optimization of glass mixture was done by adjusting the refractive index. X-ray phase and spectral-luminescent analysis of the derived composite were done. The results of these studies showed that there was no degradation of YAG: Ce powder during sintering. Dependence of luminescence intensity from temperature in the range from room temperature to 473 К was studied. It was shown, that with the phosphor in glass usage thermal quenching of luminescence was reduced in comparison with the silicone. The model of white LED was created with the "phosphor in glass" composite based on lead-silicate glasses with low temperature of vitrifying. The derived LED emits white light with a color temperature of 4370 K, and the luminous efficiency is equal to 58 lm/W. The developed luminescent composite based on the lead-silicate matrix can be used for the production of high-power white light LED.

  20. Soda-Lime-Silicate Float Glass: A Property Comparison (United States)


    Laboratory Soda-Lime-Silicate Float Glass: A Property Comparison by Andrew Cachiaras Science and Mathematics Academy at Aberdeen High School...Aberdeen, MD Luke Gilde Oak Ridge Institute for Science and Education, Oak Ridge, TN George D Quinn National Institute of Standards and...transparent armor systems. Thus, it is necessary to measure and compare the chemical composition as well as the physical and mechanical properties of

  1. Petrogenesis of the Kabanga-Musongati layered mafic-ultramafic intrusions in Burundi (Kibaran Belt): geochemical, Sr-Nd isotopic constraints and Cr-Ni behaviour


    Duchesne, Jean-Clair; Liégeois, Jean-Paul; Deblond, André; Tack, Luc


    A succession of mafic-ultramafic layered intrusions forms an alignment in the boundary zone between the Kibaran belt and the Tanzania craton. The intrusions represent a continuous series of cumulate rocks. For instance, in the Mukanda-Buhoro and Musongati (MBM) contiguous bodies, the series starts with dunite and passes to lherzolite, pyroxenite, norite, gabbronorite and anorthosite on top. Cumulate textures are conspicuous in all rock types and cryptic layering characterises cumulus mineral ...

  2. Petrogenesis and tectonomagmatic significance of Eocene mafic intrusions from the Neotethyan suture zone in the Muslim Bagh-Khanozai region, Pakistan


    Kerr, Andrew; Lavis, Owain; Kakar, M. Ishaq; McDonald, Iain


    New geochemical data for mafic intrusions within the Eocene Nisai Formation along the suture zone between the Indian and Eurasian plates are used to constrain their petrogenesis and assess the local tectonics and mantle dynamics. Petrological and geochemical data indicate that these alkalic intrusions have moderately enriched incompatible trace element compositions similar to ocean island basalt magmatism. Modelling suggests that these intrusions are the result of 1–5% melting of a deep, enri...

  3. Cleavage Energies of Modified Layered Silicates by Molecular Dynamics Simulation (United States)

    Fu, Yao-Tsung; Heinz, Hendrik


    The cleavage energy of organically modified layered silicates indicates the thermodynamic propensity of exfoliation in polymer matrices. We find substantial cleavage energy differences upon variation in cation exchange capacity (CEC) (90 and 145 meq/100g), head groups (-NH3 and --NMe3), and chain length of the surfactants (C2 to C14) due to layering effects of the surfactants in the galleries using molecular dynamics simulation. Model systems of full atomistic detail are periodic in the xy plane, open in the z direction, are subjected to sheet separation starting at equilibrium distance. Overall, the cleavage energy, consistent with experimentally measured surface tensions and previous calculations for selected organoclays, shows complex fluctuations as a function of chain length and head group structure. Computed cleavage energies are in the range 25-50 mJ/m^2 for C2˜C14 (-NH3 headgroup) and 40-200 mJ/m^2 for C2˜C14 (--NMe3 headgroup) at two CEC layered silicates. The progression is not linear and related to the packing density of the interlayer of self-assembled surfactant chains and surface reconstruction of the modified layered silicates upon cleavage.

  4. Silicate dissolution boosts the CO2 concentrations in subduction fluids. (United States)

    Tumiati, S; Tiraboschi, C; Sverjensky, D A; Pettke, T; Recchia, S; Ulmer, P; Miozzi, F; Poli, S


    Estimates of dissolved CO2 in subduction-zone fluids are based on thermodynamic models, relying on a very sparse experimental data base. Here, we present experimental data at 1-3 GPa, 800 °C, and ∆FMQ ≈ -0.5 for the volatiles and solute contents of graphite-saturated fluids in the systems COH, SiO2-COH ( + quartz/coesite) and MgO-SiO2-COH ( + forsterite and enstatite). The CO2 content of fluids interacting with silicates exceeds the amounts measured in the pure COH system by up to 30 mol%, as a consequence of a decrease in water activity probably associated with the formation of organic complexes containing Si-O-C and Si-O-Mg bonds. The interaction of deep aqueous fluids with silicates is a novel mechanism for controlling the composition of subduction COH fluids, promoting the deep CO2 transfer from the slab-mantle interface to the overlying mantle wedge, in particular where fluids are stable over melts.Current estimates of dissolved CO2 in subduction-zone fluids based on thermodynamic models rely on a very sparse experimental data base. Here, the authors show that experimental graphite-saturated COH fluids interacting with silicates at 1-3 GPa and 800 °C display unpredictably high CO2 contents.

  5. A Review: Fundamental Aspects of Silicate Mesoporous Materials

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    Zeid A. ALOthman


    Full Text Available Silicate mesoporous materials have received widespread interest because of their potential applications as supports for catalysis, separation, selective adsorption, novel functional materials, and use as hosts to confine guest molecules, due to their extremely high surface areas combined with large and uniform pore sizes. Over time a constant demand has developed for larger pores with well-defined pore structures. Silicate materials, with well-defined pore sizes of about 2.0–10.0 nm, surpass the pore-size constraint (<2.0 nm of microporous zeolites. They also possess extremely high surface areas (>700 m2 g−1 and narrow pore size distributions. Instead of using small organic molecules as templating compounds, as in the case of zeolites, long chain surfactant molecules were employed as the structure-directing agent during the synthesis of these highly ordered materials. The structure, composition, and pore size of these materials can be tailored during synthesis by variation of the reactant stoichiometry, the nature of the surfactant molecule, the auxiliary chemicals, the reaction conditions, or by post-synthesis functionalization techniques. This review focuses mainly on a concise overview of silicate mesoporous materials together with their applications. Perusal of the review will enable researchers to obtain succinct information about microporous and mesoporous materials.

  6. Development of Li+ alumino-silicate ion source

    Energy Technology Data Exchange (ETDEWEB)

    Roy, P.K.; Seidl, P.A.; Waldron, W.; Greenway, W.; Lidia, S.; Anders, A.; Kwan, J.


    To uniformly heat targets to electron-volt temperatures for the study of warm dense matter, one strategy is to deposit most of the ion energy at the peak of energy loss (dE/dx) with a low (E< 5 MeV) kinetic energy beam and a thin target[1]. Lower mass ions have a peak dE/dx at a lower kinetic energy. To this end, a small lithium (Li+) alumino-silicate source has been fabricated, and its emission limit has been measured. These surface ionization sources are heated to 1000-1150 C where they preferentially emit singly ionized alkali ions. Alumino-silicates sources of K+ and Cs+ have been used extensively in beam experiments, but there are additional challenges for the preparation of high-quality Li+ sources: There are tighter tolerances in preparing and sintering the alumino-silicate to the substrate to produce an emitter that gives uniform ion emission, sufficient current density and low beam emittance. We report on recent measurements ofhigh ( up to 35 mA/cm2) current density from a Li+ source. Ion species identification of possible contaminants is being verified with a Wien (E x B) filter, and via time-of-flight.

  7. Investigation of synthesized Be-bearing silicate glass as laboratory reference sample at X-ray electron probe microanalysis of silicates (United States)

    Belozerova, Olga Yu.; Mikhailov, Mikhail A.; Demina, Tamara V.


    The article discusses estimates of the stability and homogeneity in Be-Mg-Al-silicate glass produced by the authors and its applicability as a laboratory reference sample for X-ray electron probe microanalysis (EPMA) of Be-bearing silicate matters: crystals and quenching melt (glasses), silicates and oxides. The results were obtained using Superprobe-733 and Superprobe JXA-8200 (JEOL Ltd, Japan) devices. The sample homogeneity was studied on macro (10-100 μm) and micro (1-10 μm) levels and was evaluated by the scheme of dispersion analysis. The applicability of Be-bearing silicate glass as a reference sample for Mg, Al, Si determinations was tested on the international certified reference glasses and laboratory reference samples of minerals with a known composition. The obtained experimental metrological characteristics correspond to the "applied geochemistry" type of analysis (second category) and suggest that Be-bearing silicate glass is appropriate as a laboratory reference sample for EPMA of Be-bearing silicate matters, silicates and oxides. Using Be-Mg-Al-silicate glass as a reference sample we obtained satisfactory data on the composition of both some minerals including cordierite and beryllium cordierite, beryllium indialite, beryl and metastable phases (chrysoberyl, compounds with structure of β-quartz and petalite).

  8. Confined Water in Layered Silicates: The Origin of Anomalous Thermal Expansion Behavior in Calcium-Silicate-Hydrates. (United States)

    Krishnan, N M Anoop; Wang, Bu; Falzone, Gabriel; Le Pape, Yann; Neithalath, Narayanan; Pilon, Laurent; Bauchy, Mathieu; Sant, Gaurav


    Water, under conditions of nanoscale confinement, exhibits anomalous dynamics, and enhanced thermal deformations, which may be further enhanced when such water is in contact with hydrophilic surfaces. Such heightened thermal deformations of water could control the volume stability of hydrated materials containing nanoconfined structural water. Understanding and predicting the thermal deformation coefficient (TDC, often referred to as the CTE, coefficient of thermal expansion), which represents volume changes induced in materials under conditions of changing temperature, is of critical importance for hydrated solids including: hydrogels, biological tissues, and calcium silicate hydrates, as changes in their volume can result in stress development, and cracking. By pioneering atomistic simulations, we examine the physical origin of thermal expansion in calcium-silicate-hydrates (C-S-H), the binding agent in concrete that is formed by the reaction of cement with water. We report that the TDC of C-S-H shows a sudden increase when the CaO/SiO2 (molar ratio; abbreviated as Ca/Si) exceeds 1.5. This anomalous behavior arises from a notable increase in the confinement of water contained in the C-S-H's nanostructure. We identify that confinement is dictated by the topology of the C-S-H's atomic network. Taken together, the results suggest that thermal deformations of hydrated silicates can be altered by inducing compositional changes, which in turn alter the atomic topology and the resultant volume stability of the solids.

  9. The Magma Chamber Simulator: Modeling the Impact of Wall Rock Composition on Mafic Magmas during Assimilation-Fractional Crystallization (United States)

    Creamer, J. B.; Spera, F. J.; Bohrson, W. A.; Ghiorso, M. S.


    Although stoichiometric titration is often used to model the process of concurrent Assimilation and Fractional Crystallization (AFC) within a compositionally evolving magma body, a more complete treatment of the problem involves simultaneous and self-consistent determination of stable phase relationships and separately evolving temperatures of both Magma (M) and Wall Rock (WR) that interact as a composite M-WR system. Here we present results of M-WR systems undergoing AFC forward modeled with the Magma Chamber Simulator (MCS), which uses the phase modeling capabilities of MELTS (Ghiorso & Sack 1995) as the thermodynamic basis. Simulations begin with one of a variety of mafic magmas (e.g. HAB, MORB, AOB) intruding a set mass of Wall Rock (e.g. lherzolite, gabbro, diorite, granite, metapelite), and heat is exchanged as the M-WR system proceeds towards thermal equilibrium. Depending on initial conditions, the early part of the evolution can involve closed system FC while the WR heats up. The WR behaves as a closed system until it is heated beyond the solidus to critical limit for melt fraction extraction (fc), ranging between 0.08 and 0.12 depending on WR characteristics including composition and, rheology and stress field. Once fc is exceeded, a portion of the anatectic liquid is assimilated into the Magma. The MCS simultaneously calculates mass and composition of the mineral assemblage (Magma cumulates and WR residue) and melt (anatectic and Magma) at each T along the equilibration trajectory. Sensible and latent heat lost or gained plus mass gained by the Magma are accounted for by the MCS via governing Energy Constrained- Recharge Assimilation Fractional Crystallization (EC-RAFC) equations. In a comparison of two representative MCS results, consider a granitic WR intruded by HAB melt (51 wt. % SiO2) at liquidus T in shallow crust (0.1 GPa) with a WR/M ratio of 1.25, fc of 0.1 and a QFM oxygen buffer. In the first example, the WR begins at a temperature of 100o

  10. A 1400 km geochemical transect along the Central American Arc: Summary of mafic Holocene volcanism from Guatemala to Panama (United States)

    Geldmacher, J.; Hoernle, K.; Gill, J. B.; Hauff, F.; Heydolph, K.


    It is generally accepted that subducted oceanic crust and sediments contribute to the composition of arc magmas. Systematic variations of input parameters (including age, subduction angle, and chemical composition of the subducting material) make the Central American Volcanic Arc (CAVA), which extends from Guatemala in the northwest through El Salvador, Honduras, Nicaragua, Costa Rica and Panama to the southeast, a prime study object. We present a comprehensive (major and trace element and Sr-Nd-Pb-Hf isotope data) and consistent (all data generated in the same labs using the same methods and data reduction procedures) compilation of published and unpublished Holocene mafic volcanic rocks sampled along the entire arc. New data include Sr and, for the first time, Hf isotope data from the entire CAVA as well as major and trace element data for 43 samples from southern Nicaragua and central Costa Rica from which only isotopic compositions were previously published. The combined elemental and isotopic data confirm the influence of distinct subduction components on the composition of CAVA magmas. Along-arc geochemical variations (especially delta 208Pb/204Pb) of volcanic front magmas in Costa Rica and Panama have been explained by the different compositions of seamounts/ridges of the isotopically zoned Galápagos hotspot track that covers the subducting Cocos Plate in this sector of the arc (Hoernle et al. 2008, Nature 451). Our new data confirm this relationship with arc lavas from Costa Rica having higher 87Sr/86Sr ratios than those from western Panama reflecting a similar spatial-compositional distinction in the subducting hotspot track beneath them. In contrast, 176Hf/177Hf shows no comparable variations in this sector of the arc, indicating that the Hf is primarily derived from the mantle wedge rather than the subducting slab. Although small degree hydrous melts are believed to fertilize the mantle wedge beneath Costa Rica, residual zircon may hold back the Hf.

  11. 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.


    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

  12. Microstructure engineering of Portland cement pastes and mortars through addition of ultrafine layer silicates

    DEFF Research Database (Denmark)

    Lindgreen, Holger; Geiker, Mette Rica; Krøyer, Hanne


    Pozzolanic submicron-sized silica fume and the non-pozzolanic micron- and nano-sized layer silicates (clay minerals) kaolinite, smectite and palygorskite have been used as additives in Portland cement pastes and mortars. These layer silicates have different particle shape (needles and plates...... is that the cement paste structure and porosity can be engineered by addition of selected layer silicates having specific particle shapes and surface properties (e.g., charge and specific surface area). This seems to be due to the growth of calcium-silicate hydrates (C-S-H) on the clay particle surfaces......, and the nano-structure of the C-S-H depends on type of layer silicate. The effect of layer silicate addition is most pronounced for palygorskite and smectite having the largest surface area and negative charges on the particle surfaces. The cement pastes containing palygorskite and bentonite have...

  13. Pyrolytic Synthesis of Carbon Nanotubes from Sucrose on a Mesoporous Silicate (United States)

    Abdel-Fattah, Tarek; Siochi, Mia; Crooks, Roy


    Multiwall carbon nanotubes were synthesized from sucrose by a pyrolytic technique using mesoporous MCM-41 silicate templates without transition metal catalysts. The Nanotubes were examined in the carbon/silicate composite and after dissolution of the silicate. High resolution transmission electron microscopy study of the multiwall nanotubes showed them to be 15 nm in diameter, 200 nm in length and close-ended. There was variation in crystallinity with some nanotubes showing disordered wall structures.

  14. Proton tunneling in low dimensional cesium silicate LDS-1

    Energy Technology Data Exchange (ETDEWEB)

    Matsui, Hiroshi, E-mail:; Iwamoto, Kei [Department of Physics, Graduate School of Science, Tohoku University, Sendai 980-8578 (Japan); Mochizuki, Dai [Interdisciplinary Cluster for Cutting Edge Research, Center for Energy and Environmental Science, Shinshu University, 3-15-1 Tokida, Ueda, Nagano 386-8567 (Japan); Osada, Shimon; Asakura, Yusuke [Department of Applied Chemistry, Faculty of Science and Engineering, Waseda University, Tokyo 169-8555 (Japan); Kuroda, Kazuyuki [Department of Applied Chemistry, Faculty of Science and Engineering, Waseda University, Tokyo 169-8555 (Japan); Kagami Memorial Research Institute for Material Science and Technology, Waseda University, Tokyo 169-0051 (Japan)


    In low dimensional cesium silicate LDS-1 (monoclinic phase of CsHSi{sub 2}O{sub 5}), anomalous infrared absorption bands observed at 93, 155, 1210, and 1220 cm{sup −1} are assigned to the vibrational mode of protons, which contribute to the strong hydrogen bonding between terminal oxygen atoms of silicate chain (O–O distance = 2.45 Å). The integrated absorbance (oscillator strength) for those modes is drastically enhanced at low temperatures. The analysis of integrated absorbance employing two different anharmonic double-minimum potentials makes clear that proton tunneling through the potential barrier yields an energy splitting of the ground state. The absorption bands at 93 and 155 cm{sup −1}, which correspond to the different vibrational modes of protons, are attributed to the optical transition between the splitting levels (excitation from the ground state (n = 0) to the first excited state (n = 1)). Moreover, the absorption bands at 1210 and 1220 cm{sup −1} are identified as the optical transition from the ground state (n = 0) to the third excited state (n = 3). Weak Coulomb interactions in between the adjacent protons generate two types of vibrational modes: symmetric mode (93 and 1210 cm{sup −1}) and asymmetric mode (155 and 1220 cm{sup −1}). The broad absorption at 100–600 cm{sup −1} reveals an emergence of collective mode due to the vibration of silicate chain coupled not only with the local oscillation of Cs{sup +} but also with the proton oscillation relevant to the second excited state (n = 2)


    Energy Technology Data Exchange (ETDEWEB)

    Young, Cindy L.; Wray, James J. [School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA (United States); Clark, Roger N. [Planetary Science Institute, Tucson, AZ (United States); Spencer, John R. [Southwest Research Institute, Boulder, CO (United States); Jennings, Donald E. [NASA Goddard Space Flight Center, Greenbelt, MD (United States); Hand, Kevin P.; Carlson, Robert W. [Jet Propulsion Laboratory, Pasadena, CA (United States); Poston, Michael J. [Caltech, Pasadena, CA (United States)


    We present the first spectral features obtained from Cassini’s Composite Infrared Spectrometer (CIRS) for any icy moon. The spectral region covered by CIRS focal planes (FP) 3 and 4 is rich in emissivity features, but previous studies at these wavelengths have been limited by low signal-to-noise ratios (S/Ns) for individual spectra. Our approach is to average CIRS FP3 spectra to increase the S/N and use emissivity spectra to constrain the composition of the dark material on Iapetus. We find an emissivity feature at ∼855 cm{sup −1} and a possible doublet at 660 and 690 cm{sup −1} that do not correspond to any known instrument artifacts. We attribute the 855 cm{sup −1} feature to fine-grained silicates, similar to those found in dust on Mars and in meteorites, which are nearly featureless at shorter wavelengths. Silicates on the dark terrains of Saturn’s icy moons have been suspected for decades, but there have been no definitive detections until now. Serpentines reported in the literature at ambient temperature and pressure have features near 855 and 660 cm{sup −1}. However, peaks can shift depending on temperature and pressure, so measurements at Iapetus-like conditions are necessary for more positive feature identifications. As a first investigation, we measured muscovite at 125 K in a vacuum and found that this spectrum does match the emissivity feature near 855 cm{sup −1} and the location of the doublet. Further measurements are needed to robustly identify a specific silicate, which would provide clues regarding the origin and implications of the dark material.

  16. Light-cured Tricalcium Silicate Toxicity to the Dental Pulp. (United States)

    Jeanneau, Charlotte; Laurent, Patrick; Rombouts, Charlotte; Giraud, Thomas; About, Imad


    Numerous studies reported dentin bridge formation after pulp capping with tricalcium silicates. By contrast, pulp capping with resins leads to pulp toxicity and inflammation. Hybrid materials made up of tricalcium silicates and resins have also been developed to be used in direct pulp capping. This work was designed to study the consequences of adding resins to tricalcium silicates by investigating TheraCal (BISCO, Lançon De Provence, France) and Biodentine (Septodont, Saint Maur des Fosses, France) interactions with the dental pulp. Media conditioned with the biomaterials were used to analyze pulp fibroblast proliferation using the MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) test and proinflammatory cytokine interleukin 8 (IL-8) secretion using the enzyme-linked immunosorbent assay. The effects of conditioned media on dentin sialoprotein (DSP) and nestin expression by dental pulp stem cells (DPSCs) were investigated by immunofluorescence. The materials' interactions with the vital pulp were investigated using the entire tooth culture model. TheraCal-conditioned media significantly decreased pulp fibroblast proliferation, whereas no effect was observed with Biodentine. When DPSCs were cultured with Biodentine-conditioned media, immunofluorescence showed an increased expression of DSP and nestin. This expression was lower with TheraCal, which significantly induced proinflammatory IL-8 release both in cultured fibroblasts and entire tooth cultures. This IL-8 secretion increase was not observed with Biodentine. Entire tooth culture histology showed a higher mineralization with Biodentine, whereas significant tissue disorganization was observed with TheraCal. Within the limits of these preclinical results, resin-containing TheraCal cannot be recommended for direct pulp capping. Copyright © 2017 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  17. Low- 18O silicic magmas: why are they so rare? (United States)

    Balsley, Steven D.; Gregory, Robert T.


    Low- 18O silicic magmas are reported from only a small number of localities (e.g., Yellowstone and Iceland), yet petrologic evidence points to upper crustal assimilation coupled with fractional crystallization (AFC) during magma genesis for nearly all silicic magmas. The rarity of low- 18O magmas in intracontinental caldera settings is remarkable given the evidence of intense low- 18O meteoric hydrothermal alteration in the subvolcanic remnants of larger caldera systems. In the Platoro caldera complex, regional ignimbrites (150-1000 km 3) have plagioclase δ 18O values of 6.8±0.1‰, whereas the Middle Tuff, a small-volume (est. 50-100 km 3) post-caldera collapse pyroclastic sequence, has plagioclase δ 18O values between 5.5 and 6.8‰. On average, the plagioclase phenocrysts from the Middle Tuff are depleted by only 0.3‰ relative to those in the regional tuffs. At Yellowstone, small-volume post-caldera collapse intracaldera rhyolites are up to 5.5‰ depleted relative to the regional ignimbrites. Two important differences between the Middle Tuff and the Yellowstone low- 18O rhyolites elucidate the problem. Middle Tuff magmas reached water saturation and erupted explosively, whereas most of the low- 18O Yellowstone rhyolites erupted effusively as domes or flows, and are nearly devoid of hydrous phenocrysts. Comparing the two eruptive types indicates that assimilation of low- 18O material, combined with fractional crystallization, drives silicic melts to water oversaturation. Water saturated magmas either erupt explosively or quench as subsurface porphyries before the magmatic 18O can be dramatically lowered. Partial melting of low- 18O subvolcanic rocks by near-anhydrous magmas at Yellowstone produced small-volume, low- 18O magmas directly, thereby circumventing the water saturation barrier encountered through normal AFC processes.

  18. Low-(18)O Silicic Magmas: Why Are They So Rare?

    Energy Technology Data Exchange (ETDEWEB)

    Balsley, S.D.; Gregory, R.T.


    LOW-180 silicic magmas are reported from only a small number of localities (e.g., Yellowstone and Iceland), yet petrologic evidence points to upper crustal assimilation coupled with fractional crystallization (AFC) during magma genesis for nearly all silicic magmas. The rarity of 10W-l `O magmas in intracontinental caldera settings is remarkable given the evidence of intense 10W-l*O meteoric hydrothermal alteration in the subvolcanic remnants of larger caldera systems. In the Platoro caldera complex, regional ignimbrites (150-1000 km3) have plagioclase 6180 values of 6.8 + 0.1%., whereas the Middle Tuff, a small-volume (est. 50-100 km3) post-caldera collapse pyroclastic sequence, has plagioclase 8]80 values between 5.5 and 6.8%o. On average, the plagioclase phenocrysts from the Middle Tuff are depleted by only 0.3%0 relative to those in the regional tuffs. At Yellowstone, small-volume post-caldera collapse intracaldera rhyolites are up to 5.5%o depleted relative to the regional ignimbrites. Two important differences between the Middle Tuff and the Yellowstone 10W-180 rhyolites elucidate the problem. Middle Tuff magmas reached water saturation and erupted explosively, whereas most of the 10W-l 80 Yellowstone rhyolites erupted effusively as domes or flows, and are nearly devoid of hydrous phenocrysts. Comparing the two eruptive types indicates that assimilation of 10W-180 material, combined with fractional crystallization, drives silicic melts to water oversaturation. Water saturated magmas either erupt explosively or quench as subsurface porphyrins bejiire the magmatic 180 can be dramatically lowered. Partial melting of low- 180 subvolcanic rocks by near-anhydrous magmas at Yellowstone produced small- volume, 10W-180 magmas directly, thereby circumventing the water saturation barrier encountered through normal AFC processes.

  19. Synthesis of magnesium silicate from wheat husk ash: Effects of parameters on structural and surface properties


    Pinar Terzioglu; Sevil Yucel


    In the present study, magnesium silicate was produced by using wheat husk ash. Wheat husk was burned at 600 °C to obtain an amorphous ash structure, and the ash was processed with sodium hydroxide solution with heat to extract silica. Sodium silicate solution and magnesium salts were used to synthesize magnesium silicate. The present study investigates effects of the feeding rate on magnesium silicate production (0.6 mL/min, 35 mL/min, 70 mL/min), the type of magnesium salt (MgSO4 • 7H2O or M...

  20. Studies on Thermal Degradation Behavior of Siliceous Agriculture Waste (Rice Husk, Wheat Husk and Bagasse)

    National Research Council Canada - National Science Library

    Syed H. Javed; Umair Aslam; Mohsin Kazmi; Masooma Rustam; Sheema Riaz; Zahid Munir


    Various siliceous agriculture waste (SAW) such as rice husk, wheat husk and bagasse have been investigated to study their thermal degradation behavior using Thermogravimetric Analyzer (TGA) technique...

  1. High-temperature silicate volcanism on Jupiter's moon Io (United States)

    McEwen, A.S.; Keszthelyi, L.; Spencer, J.R.; Schubert, G.; Matson, D.L.; Lopes-Gautier, R.; Klaasen, K.P.; Johnson, T.V.; Head, J.W.; Geissler, P.; Fagents, S.; Davies, A.G.; Carr, M.H.; Breneman, H.H.; Belton, M.J.S.


    Infrared wavelength observations of Io by the Galileo spacecraft show that at last 12 different vents are erupting lavas that are probably hotter than the highest temperature basaltic eruptions on Earth today. In at least one case, the eruption near Pillan Patea, two independent instruments on Galileo show that the lava temperature must have exceeded 1700 kelvin and may have reached 2000 kelvin. The most likely explanation is that these lavas are ultramafic (magnesium-rich) silicates, and this idea is supported by the tentative identification of magnesium-rich orthopyroxene in lava flows associated with thse high-temperature hot spots.

  2. Alkali-metal silicate binders and methods of manufacture (United States)

    Schutt, J. B. (Inventor)


    A paint binder is described which uses a potassium or sodium silicate dispersion having a silicon dioxide to alkali-metal oxide mol ratio of from 4.8:1 to 6.0:1. The binder exhibits stability during both manufacture and storage. The process of making the binder is predictable and repeatable and the binder may be made with inexpensive components. The high mol ratio is achieved with the inclusion of a silicon dioxide hydrogel. The binder, which also employs a silicone, is in the final form of a hydrogel sol.

  3. Calcium silicate hydrates: Solid and liquid phase composition


    Lothenbach Barbara; Nonat André


    © 2015 Elsevier Ltd. This paper presents a review on the relationship between the composition the structure and the solution in which calcium silicate hydrate (C S H) is equilibrated. The silica chain length in C S H increases with the silicon concentration and the calcium content in the interlayer space with the calcium concentrations. Sodium and potassium are taken up in the interlayer space preferentially at low calcium concentrations and thus by low Ca/Si C S H. Aluminium uptake in C S H ...

  4. Space Weathering of Silicate Asteroids: An Observational Investigation (United States)

    MacLennan, Eric M.; Emery, Joshua; Lindsay, Sean S.


    Solar wind exposure and micrometeoroid bombardment are known to cause mineralogical changes in the upper few microns of silicate grains (by forming amorphous “composition” rims with embedded nano-phase Fe0). These processes, jointly called space weathering (SW), affect the light-scattering properties and subsequently the geometric albedo and spectral parameters (spectral slope and band depth). Earth’s Moon exhibits the well known “lunar-style” of SW: albedo decrease, spectral slope increase, and absorption band suppression. However, space mission images of (243) Ida and (433) Eros suggest that different SW “styles” exist among the silicate-bearing (olivine and pyroxene) S-complex asteroids, which exhibit diagnostic absorption features near 1 & 2 μm. While Eros generally shows only albedo differences between younger and older locations, Ida’s surface only shows changes in spectral slope and band depth. It is not clear if these SW styles are unique to Ida and Eros or if they can be observed throughout the entire asteroid population.We hypothesize that the SW styles seen on Eros and Ida also exist on other asteroid surfaces. Additionally, we hypothesize that increased solar wind exposure, smaller regolith particles, higher olivine abundance, and older asteroid surfaces will increase the observed degree of SW. Our dataset includes publicly available Visible (0.4-0.8 μm) and Near Infrared (~0.7-2.5 μm) reflectance spectra of silicate-bearing asteroids (those with 1 & 2 μm bands) from the PDS and the SMASS, S3OS2 and MIT-UH-IRTF spectral surveys. We have also conducted a spectral survey with the IRTF/SpeX targeting 52 silicate asteroids for which we have constraints for regolith grain sizes from interpretation of thermal-IR data. The relevant band parameters to SW and to interpreting mineralogical properties are calculated using the band analysis code, SARA. Geometric albedos are calculated using thermal-IR data from WISE/NEOWISE. Using these derived

  5. Infrared spectroscopy and hydrogen isotope geochemistry of hydrous silicate glasses

    Energy Technology Data Exchange (ETDEWEB)

    Epstein, S.; Stolper, E.


    The focus of this project is the combined appication of infrared spectroscopy and stable isotope geochemistry to the study of hydrogen-bearing species dissolved in silicate melts and glasses. We are conducting laboratory experiments aimed at determining the fractionation of D and H between melt species (OH and H{sub 2}O) and hydrous vapor and the diffusivities of these species in glasses and melts. Knowledge of these parameters is critical to understanding the behavior of hydrogen isotopes during igneous processes and hydrothermal processes. These results also could be valuable in application of glass technology to development of nuclear waste disposal strategies.

  6. Tin in silicate glasses: structure, thermodynamics and kinetics

    Energy Technology Data Exchange (ETDEWEB)

    Jung, Verena; Ksenofontov, Vadim [Johannes Gutenberg-Universitaet Mainz, Institut fuer Anorganische Chemie und Analytische Chemie (Germany); Aigner, Maria-Louisa; Pfeiffer, Thomas; Sprenger, Dirk [Schott AG Mainz (Germany); Felser, Claudia, E-mail: [Johannes Gutenberg-Universitaet Mainz, Institut fuer Anorganische Chemie und Analytische Chemie (Germany)


    In this work Moessbauer spectroscopy is used to investigate the oxidation states and structures of tin in silicate glasses. Thermal treatment of the glasses in atmospheres with varying oxygen partial pressure leads to the simultaneous appearance of reduction and diffusion. Experiments with varying treatment time give the opportunity to study diffusion and reduction processes in detail. Comparison of the hyperfine parameters of reference materials with measured parameter provides information about the local surroundings of the tin atoms. An octahedral surrounding for Sn{sup 4+} is presumed, while Sn{sup 2+} and three oxygen atoms form a tetrahedral coordination.

  7. Infrared Spectroscopy and Stable Isotope Geochemistry of Hydrous Silicate Glasses

    Energy Technology Data Exchange (ETDEWEB)

    Stolper, Edward


    The focus of this DOE-funded project has been the study of volatile components in magmas and the atmosphere. Over the twenty-one year period of this project, we have used experimental petrology and stable isotope geochemistry to study the behavior and properties of volatile components dissolved in silicate minerals and melts and glasses. More recently, we have also studied the concentration and isotopic composition of CO2 in the atmosphere, especially in relation to air quality issues in the Los Angeles basin.

  8. Calorimetric signature of structural heterogeneity in a ternary silicate glass

    DEFF Research Database (Denmark)

    Zhang, Yanfei; Yang, G.; Yue, Yuanzheng


    We investigate the structural heterogeneity in a silicate glass by hyperquenching–annealing–calorimetry approach. The results show a striking phenomenon: two separated sub-Tg relaxation peaks appear on the calorimetric curve of the hyperquenched CaO–MgO–SiO2 glass, implying the existence of two...... distinct structural domains of higher and lower potential energies, respectively. The higher energy domains in nanoscale are so unstable that they become ordered during hyperquenching. This is verified by the high-resolution transmission electron microscopy image exhibiting nanoordered domains in the glass...

  9. Competitive Adsorption of Arsenite and Silicic Acid on Goethite


    Luxton, Todd Peter


    The adsorption behavior of silicic acid and arsenite alone and competitively on goethite over a broad pH range (3-11) at environmentally relevant concentrations was investigated utilizing pH adsorption data and zeta potential measurements. Both addition scenarios (Si before As(III) and As(III) before Si) were examined. The results of the adsorption experiments and zeta potential measurements were then used to model the single ion and competitive ion adsorption on goethite with the CD-MUSIC ...

  10. The Asama igneous complex, central Japan: An ultramafic-mafic layered intrusion in the Mikabu greenstone belt, Sambagawa metamorphic terrain (United States)

    Agata, T.


    The Asama igneous complex comprises layered mafic and ultramafic plutonic rocks exposed over about 500×6000 m in the Mikabu greenstone belt, Sambagawa metamorphic terrain of Mie Prefecture; its margins terminate by faults, and there is no trace of chilled rocks. The exposed layered sequence is about 460 m thick, and includes dunite, plagioclase wehrlite, olivine gabbro and two-pyroxene gabbro. The crystallization sequence of essential cumulus minerals is olivine, followed by plagioclase and clinopyroxene together, and finally the appearance of orthopyroxene. Olivine systematically varies in composition from Fo 89 to Fo 78 with stratigraphic height in the lower to middle portion of the layered sequence. The composition of clinopyroxene changes from Ca 49Mg 46Fe 5 to Ca 40Mg 47Fe 13 upward in the layered sequence; cumulus orthopyroxene, which occurs at the top of the exposed layered sequence, has a composition of Ca 2Mg 74Fe 24. Cumulus chromite occurs as disseminated grains in peridotitic rocks, and tends to increase its {Fe3+}/{(Cr+Al+Fe 3+) } ratio with stratigraphic height. The most aluminous chromite [ {Cr}/{(Cr+Al)} = 0.48 ] occurs in dunite that crystallized shortly before plagioclase began to separate as an essential phase. The {Cr}/{(Cr+Al)} ratio of the most aluminous chromite, coupled with the crystallization order of essential minerals, suggests that the Asama parental magma was moderately enriched in plagioclase and clinopyroxene components in the normative mineral diagram plagioclase-clinopyroxene-orthopyroxene. It was similar to a Hawaiian tholeiite and different from the Bushveld and Great "Dyke" parental magmas that were more enriched in orthopyroxene component; it also differed from mid-oceanic ridge basalts that are more depleted in the orthopyroxene component. The Asama clinopyroxene and chromite show characteristically high TiO 2 contents and are also similar to those in Hawaiian tholeiites. The Asama igneous complex probably resulted from the

  11. Volatile contents of mafic-to-intermediate magmas at San Cristóbal volcano in Nicaragua (United States)

    Robidoux, P.; Aiuppa, A.; Rotolo, S. G.; Rizzo, A. L.; Hauri, E. H.; Frezzotti, M. L.


    San Cristóbal volcano in northwest Nicaragua is one of the most active basaltic-andesitic stratovolcanoes of the Central American Volcanic Arc (CAVA). Here we provide novel constraints on the volcano's magmatic plumbing system, by presenting the first direct measurements of major volatile contents in mafic-to-intermediate glass inclusions from Holocene and historic-present volcanic activity. Olivine-hosted (forsterite [Fo] parental melts at 1889 μg/g, which is consistent with the less-CO2-degassed melt inclusions (MI) (> 1500 μg/g) found in Nicaragua at Cerro Negro, Nejapa, and Granada. Models of H2O and CO2 solubilities constrain the degassing pathway of magmas up to 425 MPa ( 16 km depth), which includes a deep CO2 degassing step (only partially preserved in the MI record), followed by coupled degassing of H2O and S plus crystal fractionation at magma volatile saturation pressures from ∼ 195 to < 10 MPa. The variation in volatile contents from San Cristóbal MI is interpreted to reflect (1) Holocene eruptive cycles characterized by the rapid emplacement of basaltic magma batches, saturated in volatiles, at depths of 3.8-7.4 km, and (2) the ascent of more-differentiated and cogenetic volatile-poor basaltic andesites during historic-present eruptions, having longer residence times in the shallowest (< 3.4 km) and hence coolest regions of the magmatic plumbing system. We also report the first measurements of the compositions of noble-gas isotopes (He, Ne, and Ar) in fluid inclusions in olivine and pyroxene crystals. While the measured 40Ar/36Ar ratios (300-304) and 4He/20Ne ratios (9-373) indicate some degree of air contamination, the 3He/4He ratios (7.01-7.20 Ra) support a common mantle source for Holocene basalts and historic-present basaltic andesites. The magmatic source is interpreted as generated by a primitive MORB-like mantle, that is influenced to variable extents by distinct slab fluid components for basalts (Ba/La 76 and U/Th 0.8) and basaltic

  12. Reconstruction of P-T-t metamorphic conditions from symplectites: insights from Pouso Alegre mafic rocks (Brasília Belt, Brazil) (United States)

    Tedeschi, Mahyra; Lanari, Pierre; Rubatto, Daniela; Hermann, Jörg; Pedrosa-Soares, Antônio Carlos; Dussin, Ivo; Aurélio Pinheiro, Marco; Bouvier, Anne-Sophie; Baumgartner, Lukas


    Reconstructing the metamorphic history of polycyclic tectono-metamorphic mafic rocks that preserve potential relicts of high-pressure metamorphism is challenging because such rocks are commonly retrogressed and rare in supercrustal sequences. However, pressure-temperature-time (P-T-t) information is required to obtain the paleo-geothermal gradients and thus to define those units as markers for suture zones. The mafic rocks from Pouso Alegre in the Meridional Brasília Orogen (SW-Brazil) outcrop as rare lenses within Sil-Grt gneisses, Amp-Grt orthogneisses and Bt granites. They are heavily weathered. They have previously been defined as "retro-eclogites", based on the characteristic symplectite texture and some mineralogical observations. They have been intepreted to mark the suture zone between the Paranapanema and São Francisco cratons, although no quantitative estimates of the pressure is available to support this conclusion. In this study we investigated in detail these samples to refine their P-T-t history. As commonly observed in retrogressed eclogites, the studied mafic rock shows symplectite and corona textures overprinting the former paragenesis of Garnet (Grt) - Clinopyroxene (Cpx) 1 - Amphibole (Amp) 1 - Rutile (Rt). Phase equilibrium modelling shows that this assemblage is stable at 690°C and 13.5 kbar, in line with Zr-in-rutile thermometry (720 ±30° C). Local compositions of the symplectite domains were used to retrieve the jadeite content of Cpx1. This low-Jd cpx is in line with the predictions of the model and confirms a maximum pressure of 14 kbar. The symplectite formed from the reaction Cpx1+Qz+H2O→Cpx2+Amp+Pl+Qz taking place at conditions of 600-750°C and <7 kbar. Zircon and monazite U-Th-Pb geochronology was performed for the mafic and surrounding rocks. Zircon core dates from the mafic rock spread along concordia from ca. 1.7 to 1.0 Ga with a cluster at 1520±17 Ma, which is interpreted as the protolith crystallization age. Zircon rim

  13. NMR study of hydrated calcium silicates; Etude par RMN de la structure des silicates de calcium hydrates

    Energy Technology Data Exchange (ETDEWEB)

    Klur, I


    Radioactive wastes storage methods are developed by the CEA. As cements are important materials as well for hours living radioisotopes than for years living radioisotopes, a better knowledge of this material will allow to anticipate its behaviour and to obtain safer storage methods. The structure of calcium silicates (C-S-H) (main constituent of cements) have then been determined in this thesis by nuclear magnetic resonance. This method has allow to explain in structural terms, the different calcium rates that can be measured in the C-S-H too. (O.M.) 101 refs.

  14. Enhanced bioactivity of glass ionomer cement by incorporating calcium silicates. (United States)

    Chen, Song; Cai, Yixiao; Engqvist, Håkan; Xia, Wei


    Glass ionomer cements (GIC) are known as a non-bioactive dental cement. During setting the GIC have an acidic pH, driven by the acrylic acid component. It is a challenge to make GIC alkaline without disturbing its mechanical properties. One strategy was to add slowly reacting systems with an alkaline pH. The aim of the present study is to investigate the possibility of forming a bioactive dental material based on the combination of glass ionomer cement and calcium silicates. Two types of GIC were used as control. Wollastonite (CS also denoted β-CaSiO3) or Mineral Trioxide Aggregate (MTA) was incorporated into the 2 types of GIC. The material formulations' setting time, compressive strength, pH and bioactivity were compared between modified GIC and GIC control. Apatite crystals were found on the surfaces of the modified cements but not on the control GIC. The compressive strength of the cement remained with the addition of 20% calcium silicate or 20% MTA after one day immersion. In addition, the compressive strength of GIC modified with 20% MTA had been increased during the 14 d immersion (p < 0 .05).

  15. Anionic silicate organic frameworks constructed from hexacoordinate silicon centres (United States)

    Roeser, Jérôme; Prill, Dragica; Bojdys, Michael J.; Fayon, Pierre; Trewin, Abbie; Fitch, Andrew N.; Schmidt, Martin U.; Thomas, Arne


    Crystalline frameworks composed of hexacoordinate silicon species have thus far only been observed in a few high pressure silicate phases. By implementing reversible Si-O chemistry for the crystallization of covalent organic frameworks, we demonstrate the simple one-pot synthesis of silicate organic frameworks based on octahedral dianionic SiO6 building units. Clear evidence of the hexacoordinate environment around the silicon atoms is given by 29Si nuclear magnetic resonance analysis. Characterization by high-resolution powder X-ray diffraction, density functional theory calculation and analysis of the pair-distribution function showed that those anionic frameworks—M2[Si(C16H10O4)1.5], where M = Li, Na, K and C16H10O4 is 9,10-dimethylanthracene-2,3,6,7-tetraolate—crystallize as two-dimensional hexagonal layers stabilized in a fully eclipsed stacking arrangement with pronounced disorder in the stacking direction. Permanent microporosity with high surface area (up to 1,276 m2 g-1) was evidenced by gas-sorption measurements. The negatively charged backbone balanced with extra-framework cations and the permanent microporosity are characteristics that are shared with zeolites.

  16. Enhanced bioactivity of glass ionomer cement by incorporating calcium silicates (United States)

    Chen, Song; Cai, Yixiao; Engqvist, Håkan; Xia, Wei


    Abstract Glass ionomer cements (GIC) are known as a non-bioactive dental cement. During setting the GIC have an acidic pH, driven by the acrylic acid component. It is a challenge to make GIC alkaline without disturbing its mechanical properties. One strategy was to add slowly reacting systems with an alkaline pH. The aim of the present study is to investigate the possibility of forming a bioactive dental material based on the combination of glass ionomer cement and calcium silicates. Two types of GIC were used as control. Wollastonite (CS also denoted β-CaSiO3) or Mineral Trioxide Aggregate (MTA) was incorporated into the 2 types of GIC. The material formulations’ setting time, compressive strength, pH and bioactivity were compared between modified GIC and GIC control. Apatite crystals were found on the surfaces of the modified cements but not on the control GIC. The compressive strength of the cement remained with the addition of 20% calcium silicate or 20% MTA after one day immersion. In addition, the compressive strength of GIC modified with 20% MTA had been increased during the 14 d immersion (p < 0 .05). PMID:26787304

  17. Novel understanding of calcium silicate hydrate from dilute hydration

    KAUST Repository

    Zhang, Lina


    The perspective of calcium silicate hydrate (C-S-H) is still confronting various debates due to its intrinsic complicated structure and properties after decades of studies. In this study, hydration at dilute suspension of w/s equaling to 10 was conducted for tricalcium silicate (C3S) to interpret long-term hydration process and investigate the formation, structure and properties of C-S-H. Based on results from XRD, IR, SEM, NMR and so forth, loose and dense clusters of C-S-H with analogous C/S ratio were obtained along with the corresponding chemical formulae proposed as Ca5Si4O13∙6.2H2O. Crystalline structure inside C-S-H was observed by TEM, which was allocated at the foil-like proportion as well as the edge of wrinkles of the product. The long-term hydration process of C3S in dilute suspension could be sketchily described as migration of calcium hydroxide and in-situ growth of C-S-H with equilibrium silicon in aqueous solution relatively constant and calcium varied.

  18. Anionic silicate organic frameworks constructed from hexacoordinate silicon centres. (United States)

    Roeser, Jérôme; Prill, Dragica; Bojdys, Michael J; Fayon, Pierre; Trewin, Abbie; Fitch, Andrew N; Schmidt, Martin U; Thomas, Arne


    Crystalline frameworks composed of hexacoordinate silicon species have thus far only been observed in a few high pressure silicate phases. By implementing reversible Si-O chemistry for the crystallization of covalent organic frameworks, we demonstrate the simple one-pot synthesis of silicate organic frameworks based on octahedral dianionic SiO6 building units. Clear evidence of the hexacoordinate environment around the silicon atoms is given by (29)Si nuclear magnetic resonance analysis. Characterization by high-resolution powder X-ray diffraction, density functional theory calculation and analysis of the pair-distribution function showed that those anionic frameworks-M2[Si(C16H10O4)1.5], where M = Li, Na, K and C16H10O4 is 9,10-dimethylanthracene-2,3,6,7-tetraolate-crystallize as two-dimensional hexagonal layers stabilized in a fully eclipsed stacking arrangement with pronounced disorder in the stacking direction. Permanent microporosity with high surface area (up to 1,276 m(2) g(-1)) was evidenced by gas-sorption measurements. The negatively charged backbone balanced with extra-framework cations and the permanent microporosity are characteristics that are shared with zeolites.

  19. The structure of alkali silicate gel by total scattering methods

    KAUST Repository

    Benmore, C.J.


    The structure of the alkali silicate gel (ASR) collected from the galleries of Furnas Dam in Brazil was determined by a pair distribution function (PDF) analysis of high energy X-ray diffraction data. Since this method is relatively new to concrete structure analysis a detailed introduction on the PDF method is given for glassy SiO2. The bulk amorphous structure of the dam material is confirmed as no Bragg peaks are observed in the scattered intensity. The real space results show that the local structure of the amorphous material is similar to kanemite (KHSi2O5:3H2O) however the long range layer structure of the crystal is broken up in the amorphous state, so that ordering only persists of the length scale of a few polyhedra. The silicate layer structure is a much more disordered than predicted by molecular dynamics models. The X-ray results are consistent with the molecular dynamics model of Kirkpatrick et al. (2005) [1] which predicts that most of the water resides in pores within the amorphous network rather than in layers. The total scattering data provide a rigorous basis against which other models may also be tested. © 2010.

  20. Evidence of yttrium silicate inclusions in YSZ-porcelain veneers. (United States)

    Stoner, Brian R; Griggs, Jason A; Neidigh, John; Piascik, Jeffrey R


    This report introduces the discovery of crystalline defects that can form in the porcelain veneering layer when in contact with yttria-stabilized zirconia (YSZ). The focus was on dental prostheses and understanding the defects that form in the YSZ/porcelain system; however the data reported herein may have broader implications toward the use and stability of YSZ-based ceramics in general. Specimens were cut from fully sintered YSZ plates and veneering porcelain was applied (veneer. Local EDAX (SEM) was performed in the regions of visible inclusions and showed significant increases in yttrium concentration. TEM specimens also showed apparent inclusions in the porcelain and selected area electron diffraction was performed on these regions and found the inclusions to be crystalline and identified as either yttrium-silicate (Y2 SiO5 ) or yttrium-disilicate (Y2 Si2 O7 ). Micro-CT data showed that yttrium-silicate precipitates were distributed throughout the thickness of the porcelain veneer. Future studies are needed to determine whether many of the premature failures associated with this materials system may be the result of crystalline flaws that form as a result of high temperature yttrium diffusion near the surfaces of YSZ. © 2013 Wiley Periodicals, Inc.

  1. In vitro bioactivity of a tricalcium silicate cement

    Energy Technology Data Exchange (ETDEWEB)

    Morejon-Alonso, L.; Bareiro, O.; Santos, L.A. dos, E-mail: loreley.morejon@ufrgs.b [Universidade Federal do Rio Grande do Sul (UFRG), Porto Alegre, RS (Brazil). Escola de Engenharia. Dep. de Materiais; Carrodeguas R, Garcia [Consejo Superior de Investigaciones Cientificas (CSIC), Madrid (Spain). Inst. de Ceramica y Vidrio. Dept. de Ceramica


    Tricalcium silicate is the major constituent of Portland cement and the responsible for their mechanical strength at early stages. In order to be used as and additive of conventional calcium phosphate cement (CPC), in vitro bioactivity of a calcium silicate cement (CSC) after soaking in simulated body fluid (SBF) for 14 days was study. The cement was obtained by mixing Ca{sub 3}SiO{sub 5}, obtained by sol-gel process, and a Na{sub 2}HPO{sub 4} solution. The morphological and structural changes of the material before and after soaking were analyzed by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results showed the formation of a layer of a Hydroxyapatite (HA) onto the CSC cement after soaking for 1h in SBF that became denser with the increase of soaking time. The study suggests that Ca{sub 3}SiO{sub 5} would be an effective additive to improve the bioactivity and long term strength of conventional CPC. (author)

  2. Petrogenesis of the ∼500 Ma Fushui mafic intrusion and Early Paleozoic tectonic evolution of the Northern Qinling Belt, Central China (United States)

    Shi, Yu; Pei, Xiaoli; Castillo, Paterno R.; Liu, Xijun; Ding, Haihong; Guo, Zhichao


    The Fushui mafic intrusion in the Qinling orogenic belt (QOB) is composed of meta-gabbro, meta-gabbro-diorite, diorite, and syenite. Most of these rocks are metamorphosed under the upper greenschist facies to lower amphibolite facies metamorphism. Zircon separates from eight samples have LA-ICP-MS U-Pb ages of 497-501 Ma which are taken to be the emplacement age of magmas that formed the Fushui intrusion. Most of the zircon grains exhibit negative εHf values, correspond to TDM2 model ages of late Paleoproterozoic-early Mesoproterozoic or Neoproterozoic and suggest that the mafic rocks were most probably derived from mafic melts produced by partial melting of a previously metasomatized lithospheric mantle. The intrusion is not extensively contaminated by crustal materials and most chemical compositions of rocks are not modified during the greenschist to amphibolite-facies metamorhism. Rocks from the intrusion have primitive mantle-normalized trace element patterns with significant enrichment in light-REE and large ion lithophile elements (LILE) and depletion in high field-strength elements (HFSE). On the basis of the trace element contents, the Fushui intrusion was derived from parental magmas generated by <10% partial melting of both phlogopite-lherzolite and garnet-lherzolite mantle sources. These sources are best interpreted to be in a subduction-related arc environment and have been modified by fluids released from a subducting slab. The formation of the Fushui intrusion was related to the subduction of the Paleotethyan Shangdan oceanic lithosphere at ∼500 Ma.

  3. Interaction of dispersed polyvynil acetate with silicate in finishing materials

    Directory of Open Access Journals (Sweden)

    Runova, R. F.


    Full Text Available This article focuses on the processes of interaction between calcium silicate hydrates and dispersed polyvinyl acetate in tight films with the aim of developing compounds meant for restoration and finishing works. The basis of this development relies on the concept concerning the determining role of the crystal-chemical factor of the silicate phase in the formation of organic-mineral compounds of increased durability. The characteristics of dispersed calcium silicate hydrates are portrayed. The preparation conditions, accounting for the synthesis of the product of submicrocrystalline structure, conforming with the stoichiometry CaO∙SiO2 =0.8-2.0 have been determined. The interaction has been studied for compounds achieved by mixing ingredients in a rapid whirling mixer, and subjected to hardening at T=20+2 T. With the aid of XRD, DTA and Infra-Red Spectrometry methods the formation process of the sophisticated polymer silicate phase in the material was observed for a period of 90 days. The properties of the film were investigated and its high resistance against the influence of external factors was established. On this basis a conclusion concerning the quite high effectiveness of substituting portland cement with dispersed calcium silicate hydrate in polymer cement compounds has been made. White colour and other various special properties determine the suitability for repair and finishing works on facades of buildings.

    Este artículo está orientado a estudiar los procesos de interacción entre los silicatos cálcicos hidratados y el acetato de polivinilo disperso en capas impermeables, con el objeto de desarrollar compuestos destinados para la restauración. El fundamento de estos estudios es determinar el papel que los factores cristaloquímicos de las fases silicato tienen en la formación de compuestos órganominerales de elevada durabilidad. Se han descrito las características de los silicatos cálcicos hidratados

  4. 1.99 Ga mafic dykes of the Lewisian Gneiss Complex of Scotland: An upper age limit for the Palaeoproterozoic Loch Maree Group (United States)

    Baker, Thomas; Prave, Tony; Spencer, Christopher


    Mafic dyke swarms are often used as geochronological markers, as they are widespread and emplaced over short timespans. The ca. 2.4 Ga Scourie dyke swarm is one such example that has played a key role in understanding the complex tectonic and metamorphic history of the Lewisian Gneiss Complex of Scotland (LGC), part of the North Atlantic Craton (NAC). The LGC consists of Archean and Palaeoproterozoic terranes that experienced polyphase deformation prior to their assembly at ca. 1.8 Ga. Zircons separated from a doleritic dyke from the Gairloch terrane have yielded a concordant U-Th-Pb age (1,989 +4.3 / -0.99 Ma) using the ID-TIMS method. The doleritic dyke is emplaced in Lewisian gneiss that experienced both granulite and amphibolite-facies metamorphism. Partial recrystallisation and amphibolitisation of the dyke demonstrate that it pre-dates the most recent (Laxfordian) amphibolite-facies metamorphic event. The age obtained from the dyke overlaps the U-Pb age of a previously dated olivine gabbro dyke from the Assynt terrane (1,992 Ma). These combined ages provide strong corroborating evidence for a ca. 2.0 Ga mafic dyke swarm event, distinct from the older ca. 2.4 Ga Scourie dyke event known from elsewhere in the LGC. The existence of a ca. 2.0 Ga mafic dyke swarm provides an upper age limit for the Loch Maree Group (LMG), a Palaeoproterozoic succession of metasediment and metavolcanic rocks that overlie the LGC and which are not cross-cut by the Scourie dykes. This study proposes that a period of crustal extension took place in the region at ca. 2.0 Ga. Later, subduction may have resulted in the accretion of the LMG and the adjacent Ard Gneiss, which has previously been regarded as a magmatic arc. The ca. 1.9 Ga age of the earliest stage of the Laxfordian metamorphic event, which affected the LMG, could therefore mark the onset of collision. This sequence of events can be correlated with other coeval areas of the NAC, including the Nagssugtoqidian mobile belt of

  5. Timing, mantle source and origin of mafic dykes within the gravity anomaly belt of the Taihang-Da Hinggan gravity lineament, central North China Craton (United States)

    Liu, Shen; Feng, Caixia; Feng, Guangying; Xu, Mengjing; Coulson, Ian M.; Guo, Xiaolei; Guo, Zhuang; Peng, Hao; Feng, Qiang


    Six mafic dyke swarms crop out in Hebei Province within the Taihang-Da Hinggan gravity lineament magmatic belt, China, and were sampled. Here, we present new zircon laser ablation-inductively coupled plasma-mass spectrometry U-Pb age, whole rock geochemical, and Sr-Nd-Pb-Hf isotopic data for the six areas where these mafic dykes occur. The mafic (dolerite) dykes formed between 131.6 ± 1.6 and 121.6 ± 1.1 Ma, and are enriched in the light rare earth elements (LREE), some of the large ion lithophile elements (LILE; e.g., Rb, Ba, and Sr) and Pb, and are depleted in Th, U, Nb and Ta; some samples are also depleted in Eu. The dykes have high initial 87Sr/86Sr ratios (0.7055-0.7057), negative εNd (t) values (-12.5 to -11.9), relatively constant Pb isotopic ratios ((206Pb/204Pb)i = 16.45-16.51, (207Pb/204Pb)i = 15.44-15.51, (208Pb/204Pb)i = 36.49-36.53), negative εHf (t) values (-18.2 to -15.1), and old Nd (TNdDM2; 2.17-2.47 Ga) and Hf (THfDM2; 2.28-2.33 Ga) model ages. These geochronological, geochemical, and isotopic data indicate that the dykes were derived from magmas generated by low to moderate degree partial melting (1.0%-10%) of an EM1-like garnet lherzolite mantle source; these magmas fractionated olivine, clinopyroxene, and hornblende prior to emplacement, and assimilated minimal amounts of crustal material. Several possible models have previously been proposed to explain the origin of Mesozoic magmatism in this region. However, here we propose a foundering model for these studied mafic dykes, involving the foundering of eclogite from thickened lower crust due to the collision between the Siberian Craton and the North China Craon.

  6. Geochemistry and geochronology of the mafic dikes in the Taipusi area, northern margin of North China Craton: Implications for Silurian tectonic evolution of the Central Asian Orogen (United States)

    Wu, Jing-Hua; Li, Huan; Xi, Xiao-Shuang; Kong, Hua; Wu, Qian-Hong; Peng, Neng-Li; Wu, Xi-Ming; Cao, Jing-Ya; Gabo-Ratio, Jillian Aira S.


    The Taipusi area in the Bainaimiao Arc Belt is located in the northern margin of the North China Craton, at the southern margin of the middle Central Asian Orogenic Belt. It is characterized by large exposures of mafic dikes. In this contribution, we present first-hand whole-rock major and trace elements, zircon U-Pb geochronology and in situ trace element geochemistry data for these mafic rocks, which reveal their petrogenesis and tectonic evolution. These mafic dikes display varied compositions of SiO2 (49.42-54.29%), TiO2 (0.63-1.08%), Al2O3 (13.94-17.60%), MgO (4.66-10.51%), Fe2O3 (1.59-3.07%), FeO (4.60-6.90%), CaO (4.57-8.91%), Na2O (1.61-4.26%), K2O (0.92-2.54%) and P2O5 (0.11-0.29%). They are mainly of high-K calc-alkaline series with indistinct Eu anomalies, enriched in large ion lithophile elements (e.g., Rb, Ba, K and Sr) but depleted in high field strength elements (e.g., Nb, P and Ti). These suggest that the crystallizing magma was derived from enriched mantle altered by metasomatic fluids in a subduction setting with imprints of active continental margin features. The high concentrations of Hf, U, Th, Pb and Y, pronounced positive Ce but slightly negative Eu anomalies in zircons indicating that the magma underwent a fractional crystallization and crustal contamination process, with medium to high fO2. Zircon LA-ICP-MS U-Pb dating yielded concordant ages of 437-442 Ma for these mafic dikes, which is consistent with the early Paleozoic volcanic arc magmatic activity in the Bainaimiao area. Hence, we conclude that the Bainaimiao Arc Belt is a continental arc formed by the southward subduction of the Paleo-Asian ocean during early Paleozoic.

  7. P-T evolution of the Precambrian mafic rocks hosting the Varena iron ore deposit in SE Lithuania (United States)

    Šiliauskas, Laurynas; Skridlaitė, Gražina; Prusinskiene, Sabina


    The Precambrian Varena iron ore deposit in the western East European Craton, near the Latvian-East Lithuanian and Middle Lithuanian domain boundary, is buried beneath 210-500 m thick sediments. It consists of variable metasomatic rocks, mostly Mg-Fe skarns, associated with dolomitic marbles, magnetite and other ores. Metasomatites are hosted by metamorphosed igneous (mostly mafic) and sedimentary rocks and crosscut by later granites and diabase dikes. Three samples of altered mafic rocks (D8-3, D8-4 and D8-6) were chosen for PT estimations. D8-3 sample (582.5 m) is a coarse-grained metagabbro near a metasomatic K-Mg hastingsite rock. It consists of diopsidic pyroxene, edenitic and actinolitic hornblende, plagioclase (An22-15) and scapolite with minor titanite, chlorite, apatite and talc. Diopside compositions range from iron richer (Mg# 0.64, jadeite component of 0.027) to magnesium richer (Mg# 0.89, jadeite less than 0.01). Amphiboles vary from primary Mg-hastingsitic (AlVI 0.38 apfu, Mg# 0.70) to secondary edenitic (AlVI 0.25, Mg# 0.72) hornblende. Plagioclase is slightly zoned, cores more calcium-rich (An22-20) than rims (An18-15). Sample D8-4 (588 m) has similar mineral and chemical compositions, but is somewhat more altered than the D8-3 sample. Plagioclase in diopside is more anorthitic (An32-30), while matrix plagioclase is more albitic (An27-20). Sample D8-6 (710 m) is composed of diopside, plagioclase, scapolite, Mg-hornblende and actinolite. Diopside has Mg# of 0.77-0.84 and jadeite component of 0.01-0.02. Amphibole compositions range from Mg-hornblende (Mg# 0.64-0.7, Al VI 0.2-0.17 apfu) to actinolite (Mg# 0.76-0.83, Al VI 0.12-0.10 apfu). Plagioclases are An18 in cores and An10 at rims. Diopsides with the lowest Mg# and highest jadeite components, together with plagioclase cores were used for PT calculations by the winTWQ software (Berman, 1991). Temperatures of 530° C and 550° C and pressures of 6.3 and 6.1 kbar were estimated for the D8-3 and D8

  8. Influence of silicate on the transport of bacteria in quartz sand and iron mineral-coated sand. (United States)

    Dong, Zhe; Yang, Haiyan; Wu, Dan; Ni, Jinren; Kim, Hyunjung; Tong, Meiping


    The influence of silicate on the transport and deposition of bacteria (Escherichia coli) in packed porous media were examined at a constant 20 mM ionic strength with different silicate concentrations (from 0 to 1 mM) at pH 7. Transport experiments were performed in two types of representative porous media, both bare quartz sand and iron mineral-coated quartz sand. In bare quartz sand, the breakthrough plateaus in the presence of silicate in suspensions were lower and the corresponding retained profiles were higher than those without silicate ions, indicating that the presence of silicate in suspensions decreased cell transport in bare quartz sand. Moreover, the decrease of bacteria transport in quartz sand induced by silicate was more pronounced with increasing silicate concentrations from 0 to 1 mM. However, when EPS was removed from cell surfaces, the presence of silicate in cell suspensions (with different concentrations) did not affect the transport behavior of bacteria in quartz sand. The interaction of silicate with EPS on cell surfaces negatively decreased the zeta potentials of bacteria, resulting in the decreased cell transport in bare quartz sand when silicate was copresent in bacteria suspensions. In contrast, the presence of silicate in suspensions increased cell transport in iron mineral-coated sand. Silicate ions competed with bacteria for the adsorption sites on mineral-coated sand, contributing to the increased cell transport in mineral-coated sand with silicate present in cell suspensions. Copyright © 2014 Elsevier B.V. All rights reserved.

  9. A study of redox kinetic in silicate melt; Etude cinetique des reactions d'oxydoreduction dans les silicates

    Energy Technology Data Exchange (ETDEWEB)

    Magnien, V


    The aim of this thesis is to understand better iron redox reactions and mechanisms in silicate glasses and melts. Particular interest has been paid to the influence of temperature and chemical composition. For this purpose, the influence of alkali element content, iron content and network formers on the kinetics of redox reactions has been determined through XANES and Raman spectroscopy experiments performed either near the glass transition or above the liquidus temperature. As a complement, electrical conductivity and RBS spectroscopy experiments have been made to characterize the diffusivity of the species that transport electrical charges and the reaction morphology, respectively. Temperature and composition variations can induce changes in the dominating redox mechanism. At a given temperature, the parameters that exert the strongest influence on redox mechanisms are the presence or lack of divalent cations and the existing decoupling between the mobility of network former and modifier elements. Near Tg, the diffusion of divalent cations, when present in the melt, controls the kinetics of iron redox reactions along with a flux of electron holes. Composition, through the degree of polymerization and the silicate network structure, influences the kinetics and the nature of the involved cations, but not the mechanisms of the reaction. Without alkaline earth elements, the kinetics of redox reactions are controlled by the diffusion of oxygen species. With increasing temperatures, the diffusivities of all ionic species tend to become similar. The decoupling between ionic fluxes then is reduced so that several mechanisms become kinetically equivalent and can thus coexist. (author)

  10. Steam based conversion coating on AA6060 alloy: Effect of sodium silicate chemistry and corrosion performance

    DEFF Research Database (Denmark)

    Din, Rameez Ud; Bordo, Kirill; Tabrizian, Naja


    Surface treatment of aluminium alloy AA6060 using an industrially applicable pilot steam jet system with and without silicate chemistry has been investigated. Treatment using steam alone and steam with silicate, resulted in an oxide layer formation with thickness ∼425 nm and ∼160 nm, respectively...

  11. Sodium Silicate Behavior in Porous Media Applied for In-Depth Profile Modifications

    Directory of Open Access Journals (Sweden)

    Hossein A. Akhlaghi Amiri


    Full Text Available This paper addresses alkaline sodium silicate (Na-silicate behavior in porous media. One of the advantages of the Na-silicate system is its water-like injectivity during the placement stage. Mixing Na-silicate with saline water results in metal silicate precipitation as well as immediate gelation. This work demonstrated that low salinity water (LSW, sea water diluted 25 times could be used as a pre-flush in flooding operations. A water override phenomenon was observed during gel formation which is caused by gravity segregation. Dynamic adsorption tests in the sand-packed tubes showed inconsiderable adsorbed silicon density (about 8.5 × 10−10 kg/cm3 for a solution with 33 mg/L silicon content, which is less than the estimated mono-layer adsorption density of 1.4 × 10−8 kg/cm3. Na-silicate enhanced water sweep efficiency after application in a dual-permeability sand-pack system, without leak off into the oil-bearing low permeability (LP zone. Field-scale numerical sensitivity studies in a layered reservoir demonstrated that higher permeability and viscosity contrasts and lower vertical/horizontal permeability ratio result in lower Na-silicate leakoff into the matrix. The length of the mixing zone between reservoir water and the injected Na-silicate solution, which is formed by low salinity pre-flush, acts as a buffer zone.

  12. Crystal Structure and Chemical Composition of a Presolar Silicate from the Queen Elizabeth Range 99177 Meteorite (United States)

    Nguyen, A. N.; Keller, L. P.; Rahman, Z.; Messenger, S.


    Mineral characterization of presolar silicate grains, the most abundant stardust phase, has provided valuable information about the formation conditions in circumstellar environments and in super-nova (SN) outflows. Spectroscopic observations of dust around evolved stars suggest a majority of amor-phous, Mg-rich olivine grains, but crystalline silicates, most of which are pyroxene, have also been observed [1]. The chemical compositions of hundreds of presolar silicates have been determined by Auger spectroscopy and reveal high Fe contents and nonstoichiometric compositions intermediate to olivine and pyroxene [2-6]. The unexpectedly high Fe contents can partly be attributed to secondary alteration on the meteorite parent bodies, as some grains have Fe isotopic anomalies from their parent stellar source [7]. Only about 35 presolar silicates have been studied for their mineral structures and chemical compositions by transmission electron microscopy (TEM). These grains display a wide range of compositions and structures, including crystalline forsterite, crystalline pyroxene, nanocrystalline grains, and a majority of amorphous nonstoichiometric grains. Most of these grains were identified in the primitive Acfer 094 meteorite. Presolar silicates from this meteorite show a wide range of Fe-contents, suggestive of secondary processing on the meteorite parent body. The CR chondrite QUE 99177 has not suffered as much alteration [8] and displays the highest presolar silicate abundance to date among carbonaceous chondrites [3, 6]. However, no mineralogical studies of presolar silicates from this meteorite have been performed. Here we examine the mineralogy of a presolar silicate from QUE 99177.

  13. Facile synthesis of magnetic hierarchical copper silicate hollow nanotubes for efficient adsorption and removal of hemoglobin. (United States)

    Zhang, Min; Wang, Baoyu; Zhang, Yanwei; Li, Weizhen; Gan, Wenjun; Xu, Jingli


    This study reports the fabrication of magnetic copper silicate hierarchical hollow nanotubes, which are featured by a tailored complex wall structure and high surface area. Moreover, they exhibit excellent performance as an easily recycled adsorbent for protein separation. Particularly, this strategy can be extended as a general method to prepare other magnetic metal silicate hollow nanotubes.

  14. FT-IR and 29 Si-NMR for evaluating aluminium silicate precursors for geopolymers

    NARCIS (Netherlands)

    Valcke, S.L.A.; Pipilikaki, P.; Fischer, H.R.; Verkuijlen, M.H.W.; Eck, E.R.H.


    Geopolymers are systems of inorganic binders that can be used for sustainable, cementless concrete and are formed by alkali activation of an aluminium–silicate precursor (often secondary resources like fly ash or slag). The type of aluminium– silicate precursor and its potential variations within

  15. New estimates of silicate weathering rates and their uncertainties in global rivers (United States)

    Moon, Seulgi; Chamberlain, C. P.; Hilley, G. E.


    This study estimated the catchment- and global-scale weathering rates of silicate rocks from global rivers using global compilation datasets from the GEMS/Water and HYBAM. These datasets include both time-series of chemical concentrations of major elements and synchronous discharge. Using these datasets, we first examined the sources of uncertainties in catchment and global silicate weathering rates. Then, we proposed future sampling strategies and geochemical analyses to estimate accurate silicate weathering rates in global rivers and to reduce uncertainties in their estimates. For catchment silicate weathering rates, we considered uncertainties due to sampling frequency and variability in river discharge, concentration, and attribution of weathering to different chemical sources. Our results showed that uncertainties in catchment-scale silicate weathering rates were due mostly to the variations in discharge and cation fractions from silicate substrates. To calculate unbiased silicate weathering rates accounting for the variations from discharge and concentrations, we suggest that at least 10 and preferably ∼40 temporal chemical data points with synchronous discharge from each river are necessary. For the global silicate weathering rate, we examined uncertainties from infrequent sampling within an individual river, the extrapolation from limited rivers to a global flux, and the inverse model selections for source differentiation. For this weathering rate, we found that the main uncertainty came from the extrapolation to the global flux and the model configurations of source differentiation methods. This suggests that to reduce the uncertainties in the global silicate weathering rates, coverage of synchronous datasets of river chemistry and discharge to rivers from tectonically active regions and volcanic provinces must be extended, and catchment-specific silicate end-members for those rivers must be characterized. With current available synchronous datasets, we

  16. Isotope and trace element studies of the Xingdi II mafic-ultramafic complex in the northern rim of the Tarim Craton: Evidence for emplacement in a Neoproterozoic subduction zone (United States)

    Chen, Hongjin; Chen, Yanjing; Ripley, Edward M.; Li, Chusi; Deng, Xiaohua; Yue, Suwei; Zheng, Zhen; Fu, Bin


    The Xingdi II mafic-ultramafic complex is located in the northern rim of the Tarim Craton, Northern Xinjiang, NW China. This complex is mainly composed of gabbro, gabbronorite, websterite and lherzolite, plus minor granodiorites and granites. The geodynamic setting of this complex and other Neoproterozoic mafic-ultramafic complexes in the region is debated, with opinions varying from mantle plume to a continental arc. A new zircon U-Pb age from this study reveals > 7-myr difference for two gabbroic intrusive phases in the Xingdi II mafic-ultramafic complex and up to a 21-myr difference between this complex and the nearby mafic-ultramafic complexes that occur crystals from the Xingdi II mafic-ultramafic complex are between - 2.8 and - 7.0. The trace element and isotope data together indicate that this complex formed from multiple pulses of contaminated subduction-related basaltic magma that were emplaced separately with a time gap of at least 7 myr. The results from this study support the viewpoint that in the Neoproterozoic the northern rim of the Tarim Craton was an active continental margin that belongs to the Circum-Rodinia Subduction System.

  17. Influence of iron on crystallization behavior and thermal stability of the insulating materials - porous calcium silicates

    DEFF Research Database (Denmark)

    Haastrup, Sonja; Yu, Donghong; Yue, Yuanzheng


    The properties of porous calcium silicate for high temperature insulation are strongly influenced by impurities. In this work we determine the influence of Fe3+ on the crystallization behavior and thermal stability of hydrothermally derived calcium silicate. We synthesize porous calcium silicate...... by XRD analysis. The thermal stability and compressive strength of the calcium silicates are seriously influenced by the changes of their crystal structure. Linear shrinkage of the reference sample is 1.3% at 1050°C, whereas the sample with Fe/Si =1.0% does by 30.4%. In conclusion, the presence of Fe3......+ modifies the crystal structure of porous calcium silicates, leading to a significant shrinkage in these materials....

  18. Bioactivity studies of calcium magnesium silicate prepared from eggshell waste by sol–gel combustion synthesis

    Directory of Open Access Journals (Sweden)

    Rajan Choudhary


    Full Text Available The present study focused on the synthesis of calcium magnesium silicate (akermanite, Ca2MgSi2O7 using eggshell biowaste (as calcium source, magnesium nitrate and tetraethyl orthosilicate (TEOS as starting materials. Sol–gel combustion method was adopted to obtain calcium magnesium silicate. Citric acid was used as a fuel (reducing agent and nitrate ions present in the metal nitrates acts as an oxidizing agent during combustion process. The characterization of synthesized calcium magnesium silicate was carried out by powder X-ray diffraction (XRD, Fourier transform infrared (FTIR and scanning electron microscopy (SEM techniques. Calcium magnesium silicate crystallite size was observed in nano regime which can effectively mimic natural bone apatite composition. In-vitro bioactivity was investigated by immersing calcium magnesium silicate pellet in simulated body fluid (SBF for three weeks. Results show effective deposition of crystallized hydroxyapatite (HAP layer on its surface and predicting its possibilities for applications in hard tissue regeneration.

  19. Pilot study on binding of bovine salivary proteins to grit silicates and plant phytoliths. (United States)

    Mau, Marcus; M Kaiser, Thomas; Südekum, Karl-Heinz


    Mostly fed with grass in fresh or conserved form, cattle and other livestock have to cope with silicate defence bodies from plants (phytoliths) and environmental silicates (grit), which abrade tooth enamel and could additionally interact with various salivary proteins. To detect potential candidates for silicate-binding proteins, bovine whole saliva was incubated with grass-derived phytoliths and silicates. Interactions of salivary proteins with pulverized bovine dental enamel and dentine were additionally analysed. After intense washing, the powder fractions were loaded onto 1D-polyacrylamide gels, most prominent adhesive protein bands were cut out and proteins were identified by mass spectrometry within three independent replicates. All materials were mainly bound by bovine odorant-binding protein, bovine salivary protein 30×10(3) and carbonic anhydrase VI. The phytolith/silicate fraction showed additional stronger interaction with haemoglobin β and lactoperoxidase. Conceivably, the binding of these proteins to the surfaces may contribute to biological processes occurring on them.

  20. Apatite: a new redox proxy for silicic magmas? (United States)

    Miles, Andrew; Graham, Colin; Hawkesworth, Chris; Gillespie, Martin; Bromiley, Geoff; Hinton, Richard


    The oxidation states of magmas provide valuable information about the release and speciation of volatile elements during volcanic eruptions, metallogenesis, source rock compositions, open system magmatic processes, tectonic settings and potentially titanium (Ti) activity in chemical systems used for Ti-dependent geothermometers and geobarometers. In this presentation we explore the use of Mn in apatite as an oxybarometer in intermediate and silicic igneous rocks. Increased Mn concentrations in apatite in granitic rocks from the zoned Criffell granitic pluton (southern Scotland) correlate with decreasing Fe2O3 (Fe3+) and Mn in the whole-rock and likely reflect increased Mn2+/Mn3+and greater compatibility of Mn2+ relative to Mn3+ in apatite under reduced conditions. Fe3+/Fe2+ ratios in biotites have previously been used to calculate oxygen fugacities (fO2) in the outer zone granodiorites and inner zone granites where redox conditions have been shown to change from close to the magnetite-hematite buffer to close to the nickel-nickel oxide buffer respectively[1]. This trend is apparent in apatite Mn concentrations from a range of intermediate to silicic volcanic rocks that exhibit varying redox states and are shown to vary linearly and negatively with log fO2, such that logfO2=-0.0022(±0.0003)Mn(ppm)-9.75(±0.46) Variations in the Mn concentration of apatites appear to be largely independent of differences in the Mn concentration of the melt. Apatite Mn concentrations may therefore provide an independent oxybarometer that is amenable to experimental calibration, with major relevance to studies on detrital mineral suites, particularly those containing a record of early Earth redox conditions, and on the climatic impact of historic volcanic eruptions[2]. [1] Stephens, W. E., Whitley, J. E., Thirlwall, M. F. and Halliday, A. N. (1985) The Criffell zoned pluton: correlated behaviour of rare earth element abundances with isotopic systems. Contributions to Mineralogy and

  1. Role of organically modified layered silicate both as an active interfacial modifier and nanofiller for immiscible polymer blends.

    CSIR Research Space (South Africa)

    Ray, SS


    Full Text Available ) revealed efficient mixing of the polymers in the presence of organically modified layered silicate. X-ray diffraction (XRD) patterns and transmission electron microscopic (TEM) observations showed that silicate layers were either intercalated or exfoliated...

  2. Effects of Silicate, Phosphate, and Calcium on the Stability of Aldopentoses (United States)

    Nitta, Sakiko; Furukawa, Yoshihiro; Kakegawa, Takeshi


    Ribose is an important constituent of RNA: ribose connects RNA bases and forms a strand of sugar phosphates. Accumulation of ribose on prebiotic Earth was difficult because of its low stability. Improvement in the yield of ribose by the introduction of borate or silicate in a formose-like reaction has been proposed. The effects of borates have been further analyzed and confirmed in subsequent studies. Nonetheless, the effects of silicates and phosphates remain unclear. In the present study, we incubated aldopentoses in a highly alkaline aqueous solution at a moderate temperature to determine the effects of silicate or phosphate on the degradation rates of ribose and its isomeric aldopentoses. The formation of a complex of silicate (or phosphate) with ribose was also analyzed in experiments with 29Si and 31P nuclear magnetic resonance (NMR). We found that silicate or phosphate complexes of ribose were not detectable under our experimental conditions. The stability of ribose and lyxose improved after addition of 40-fold molar excess (relative to a pentose) of sodium silicate or sodium phosphate to the alkaline solution. The stability was not improved further when an 80-fold molar excess of sodium silicate or sodium phosphate was added. Calcium was removed from these solutions by precipitation of calcium salts. The drop in Ca2+ concentration might have improved the stability of ribose and lyxose, which are susceptible to aldol addition. The improvement of ribose stability by the removal of Ca2+ and by addition of silicate or phosphate was far smaller than the improvement by borate. Furthermore, all aldopentoses showed similar stability in silicate- and phosphate-containing solutions. These results clearly show that selective stabilization of ribose by borate cannot be replaced by the effects of silicate or phosphate; this finding points to the importance of borate in prebiotic RNA formation.

  3. Measurement of the efficacy of calcium silicate for the protection and repair of dental enamel. (United States)

    Parker, Alexander S; Patel, Anisha N; Al Botros, Rehab; Snowden, Michael E; McKelvey, Kim; Unwin, Patrick R; Ashcroft, Alexander T; Carvell, Mel; Joiner, Andrew; Peruffo, Massimo


    To investigate the formation of hydroxyapatite (HAP) from calcium silicate and the deposition of calcium silicate onto sound and acid eroded enamel surfaces in order to investigate its repair and protective properties. Calcium silicate was mixed with phosphate buffer for seven days and the resulting solids analysed for crystalline phases by Raman spectroscopy. Deposition studies were conducted on bovine enamel surfaces. Acid etched regions were produced on the enamel surfaces using scanning electrochemical cell microscopy (SECCM) with acid filled pipettes and varying contact times. Following treatment with calcium silicate, the deposition was visualised with FE-SEM and etch pit volumes were measured by AFM. A second set of bovine enamel specimens were pre-treated with calcium silicate and fluoride, before acid exposure with the SECCM. The volumes of the resultant acid etched pits were measured using AFM and the intrinsic rate constant for calcium loss was calculated. Raman spectroscopy confirmed that HAP was formed from calcium silicate. Deposition studies demonstrated greater delivery of calcium silicate to acid eroded than sound enamel and that the volume of acid etched enamel pits was significantly reduced following one treatment (penamel was 0.092 ± 0.008 cm/s. This was significantly reduced, 0.056 ± 0.005 cm/s, for the calcium silicate treatments (penamel surfaces. Calcium silicate can provide significant protection of sound enamel from acid challenges. Calcium silicate is a material that has potential for a new approach to the repair of demineralised enamel and the protection of enamel from acid attacks, leading to significant dental hard tissue benefits. © 2014 Elsevier Ltd. All rights reserved.

  4. Ferroan Dolomitization by Seawater Interaction with Mafic Igneous Dikes and Carbonate Host Rock at the Latemar Platform, Dolomites, Italy: Numerical Modeling of Spatial, Temporal, and Temperature Data

    Directory of Open Access Journals (Sweden)

    K. Blomme


    Full Text Available Numerous publications address the petrogenesis of the partially dolomitized Latemar carbonate platform, Italy. A common factor is interpretation of geochemical data in terms of heating via regional igneous activity that provided kinetically favorable conditions for replacement dolomitization. New field, petrographic, XRD, and geochemical data demonstrate a spatial, temporal, and geochemical link between replacement dolomite and local mafic igneous dikes that pervasively intrude the platform. Dikes are dominated by strongly altered plagioclase and clinopyroxene. Significantly, where ferroan dolomite is present, it borders dikes. We hypothesize that seawater interacted with mafic minerals, causing Fe enrichment in the fluid that subsequently participated in dolomitization. This hypothesis was tested numerically through thermodynamic (MELTS, Arxim-GEM and reactive flow (Arxim-LMA simulations. Results confirm that seawater becomes Fe-enriched during interaction with clinopyroxene (diopside-hedenbergite and plagioclase (anorthite-albite-orthoclase solid solutions. Reaction of modified seawater with limestone causes ferroan and nonferroan replacement dolomitization. Dolomite quantities are strongly influenced by temperature. At 40 to 80°C, ferroan dolomite proportions decrease with increasing temperature, indicating that Latemar dolomitization likely occurred at lower temperatures. This relationship between igneous dikes and dolomitization may have general significance due to the widespread association of carbonates with rifting-related igneous environments.

  5. Exploring Cumulates in Small, Shallow Parts of a Large Mafic Magma System to Provide Baseline Models for Crystallization in Larger Intrusions (United States)

    Srogi, L.; Willis, K. V.; Lutz, T. M.; Plank, T. A.; Pollock, M.; Connolly, B.; Wood, A. M.


    Small, shallow portions of large magmatic systems cool more rapidly and potentially have less subsolidus overprinting than large mafic intrusions, but it is unclear whether they are small-scale analogs for the same crystallization processes. The Morgantown-Jacksonwald magmatic system (MJS), western Newark Basin, Pennsylvania, is part of the 201-Ma Central Atlantic Magmatic Province (CAMP) formed during Pangean rifting. The MJS consists of several interconnected intrusions exposed in cross-section from the Jacksonwald basalt at the paleosurface to 6 km depth (variably LREE-enriched rims; some negative Eu anomalies. REE patterns calculated for liquids in equilibrium with opx using published Kd values are roughly parallel to but significantly higher than REE in host chill margin diabase. CSDs of opx and matrix plagioclase from several samples within 10m of the basal contact will be used to evaluate models of crystal growth vs. mechanical sorting. Modes and mineral compositions are not consistent with MELTS fractionation models: opx crystallizes in place of pigeonite; pyroxenes are zoned in Ca not Fe-Mg; late-crystallizing quartz and K-feldspar are lacking. These features suggest crystallization buffered by earlier phases in the crystal mush with some melt migration, similar to processes that produce more extreme layering in large mafic intrusions.

  6. Low to Extremely Low Water Abundances Measured in Nominally Anhydrous Minerals in Mafic to Granitic Apollo Rock Clasts (United States)

    Simon, J. I.; Christoffersen, R.; Wang, J.; Alexander, C. M. O'D.; Mills, R. D.; Hauri, E. H.


    Lunar sample-based volatile studies have focused on assessing the inventory and distribution of water in the Moon. Some have focused on the relatively young mare basalts and pyroclastic glasses, which result from partial melting of the relatively young lunar mantle. Less certain is the water inventory for the oldest materials available, which have the greater potential to record the earliest history of volatiles in the Moon (and thus provide evidence for the "wet" vs. "dry" accretion hypotheses of the Earth-Moon system. Studies of volatiles in ancient lunar rocks have largely focused on apatite. One recent FTIR (Fourier Transform Infrared Radiometer) study of plagioclase reported a relatively "wet" (approximately 320 parts per million) magma for primordial ferroan anorthosites (FANs). Another, a NanoSIMS study of alkali feldspar, reported a "wet" (approximately 1 weight percentage) felsic magma, but due to the differentiation processes required for silicic magmatism in the lunar crust, predicted an essentially "dry" (less than 100 parts per million) bulk Moon. Thus, despite evidence that appears to complicate the early "dry" Moon paradigm, there is no apparent unanimity among the measurements, even those on apatite. This disparity is clearly seen by the order of magnitude different water estimates for lunar "alkali-rich suite rocks" (Fig. 1). Some of the apparent differences may be explained by recent improvements in the apatite-based water estimates that better account for relative compatibilities of OH-, Cl, and F. In the present work, we seek to expand our understanding of the volatile abundances in early formed lunar magmas, their source reservoirs, and to address the potential role that felsic magmas play on the lunar hydrogen budget over time by employing NanoSIMS analysis of nominally anhydrous minerals.

  7. An AMS study of magma transport and emplacement mechanisms in mafic dykes from the Etendeka Province, Namibia (United States)

    Wiegand, Miriam; Trumbull, Robert B.; Kontny, Agnes; Greiling, Reinhard O.


    The Henties Bay Outjo dyke swarm (HOD) in NW Namibia is part of the early Cretaceous Paraná-Etendeka Large Igneous Province. The dykes are dominantly doleritic, compositionally equivalent to the erupted lava series and thus the HOD provides a look at the feeder systems of a flood basalt province. The subvertical dykes mostly strike NE-SW and minor NW-SE, parallel or perpendicular to the Damara Belt in which they intruded. We present a magnetic fabric study using the anisotropies of low-field magnetic susceptibility (AMS) and of anhysteretic remanent magnetization (AARM) with the aim to derive magma flow directions and better constrain emplacement mechanisms within the dyke swarm. Magnetic susceptibility and its anisotropy in the dykes is mainly controlled by distribution anisotropy of titanomagnetite that mimics the flow-oriented silicate fabric. The anisotropy is low in most samples, supporting a magmatic origin. In 66 of 110 investigated samples the AMS fabric is ;normal;, with the κmax axis (inferred flow orientation) within the dyke plane. Most samples yielded vertical to subvertical flow orientations regardless of location near or distant from the former rifted margin. The ;anomalous; magnetic fabrics, where κmax is inclined to the dyke plane, are attributed to two mechanisms. One is the single-domain effect of titanomagnetite, which was found by unequal orientations of AMS and AARM fabrics. The other case anomalous fabric is rotation of the AMS axes by shear within the magma, producing symmetric imbrication of AMS fabric on opposite dyke walls; or more commonly, asymmetric magnetic fabrics, which we relate to tectonic shear at the dyke walls during emplacement. Field support for syn-emplacement shear is given by dyke segmentation geometries including locally curved segment tips, en-echelon arrangements and left/right-stepping displacements. Regionally, syn-emplacement shear is consistent with the observed reactivation during Gondwana breakup of

  8. Soil microbial response to waste potassium silicate drilling fluid. (United States)

    Yao, Linjun; Naeth, M Anne; Jobson, Allen


    Potassium silicate drilling fluids (PSDF) are a waste product of the oil and gas industry with potential for use in land reclamation. Few studies have examined the influence of PSDF on abundance and composition of soil bacteria and fungi. Soils from three representative locations for PSDF application in Alberta, Canada, with clay loam, loam and sand textures were studied with applications of unused, used once and used twice PSDF. For all three soils, applying ≥40 m3/ha of used PSDF significantly affected the existing soil microbial flora. No microbiota was detected in unused PSDF without soil. Adding used PSDF to soil significantly increased total fungal and aerobic bacterial colony forming units in dilution plate counts, and anaerobic denitrifying bacteria numbers in serial growth experiments. Used PSDF altered bacterial and fungal colony forming unit ratios of all three soils. Copyright © 2015. Published by Elsevier B.V.

  9. Laboratory Evidence for Microbially Mediated Silicate Mineral Dissolution in Nature

    Energy Technology Data Exchange (ETDEWEB)

    Ullman, W. J.; Kirchman, D. L.; Welch, S. A.; Vandevivere, P.


    Bacteria may potentially enhance or inhibit silicate mineral dissolution in nature by a variety of mechanisms. In the laboratory, some microbial metabolites enhanced dissolution rates by a factor of ten above the expected proton-promoted rate by an additional ligand-promoted mechanism focused principally at Al sites at the mineral surface. In investigations with bacteria, it was found that organic acids are produced in organic-rich/nutrient-poor cultures, resulting in increased mineral dissolution rates compared to abiotic controls. Alginate and poly-aspartate inhibited dissolution rates either by a reduction in surface reactivity or reactive surface area (or both). Bacteria may also influence dissolution rates by creating and maintaining microenvironments where metabolite concentrations are higher than in the bulk solution.

  10. About Fundamental Problems of Hydrosphere and Silicate Karst

    Directory of Open Access Journals (Sweden)

    A. Ya. Gayev


    Full Text Available Rationale of hydrosphere model with two regions of supply and discharge reveals regularities of ground water formation reflecting the special features of system water – rock – gas – living material and character of interaction of hydrosphere with the other spheres of the Earth. It is necessary to concentrate the development of endogenous hy-drogeology fundamentals with the study of silicate karst on investigation of “white and black smokers”, the structure and isotope composition of water in different phase condi-tions, and on modeling of situation in hydrometagenese zone. It will support the development of geotechnology and providing the humanity with mineral and energetic resources in future.

  11. Is plant ecology more siliceous than we realise? (United States)

    Cooke, Julia; Leishman, Michelle R


    Although silicon occurs in all plants, it is an element that is largely overlooked by many plant ecologists and most plant-related research on silicon comes from agronomy, archaeology, palaeontology and biogeochemistry. Plant silicon has many functions, acting biochemically as silicic acid and physically as amorphous silica. It contributes to cell and plant strength and enables plants to respond adaptively to environmental stresses. Consequently, plant silicon can increase plant fitness in many fundamental aspects of ecology, including plant-herbivore interactions, light interception, pathogen resistance and alleviation of abiotic stresses. Here, we provide an ecological perspective to research outcomes from diverse disciplines, showing that silicon is an important element in plant ecology that is worthy of greater attention. Copyright © 2010 Elsevier Ltd. All rights reserved.

  12. Intergranular area microalloyed aluminium-silicate ceramics fractal analysis

    Directory of Open Access Journals (Sweden)

    Purenović J.


    Full Text Available Porous aluminium-silicate ceramics, modified by alloying with magnesium and microalloying with alluminium belongs to a group of advanced multifunctional ceramics materials. This multiphase solid-solid system has predominantly amorphous microstructure and micro morphology. Intergranular and interphase areas are very complex, because they represent areas, where numbered processes and interactions take place, making new boundaries and regions with fractal nature. Fractal analysis of intergranular microstructure has included determination of ceramic grain fractal dimension by using Richardson method. Considering the fractal nature of intergranular contacts, it is possible to establish correlation between material electrical properties and fractal analysis, as a tool for future correlation with microstructure characterization. [Projekat Ministarstva nauke Republike Srbije, br. ON 172057 i br. III 45012

  13. Stylolites, porosity, depositional texture, and silicates in chalk facies sediments

    DEFF Research Database (Denmark)

    Fabricius, Ida Lykke; Borre, Mai K.


    Comparison of chalk on the Ontong Java Plateau and chalk in the Central North Sea indicates that, whereas pressure dissolution is controlled by effective burial stress, pore-filling cementation is controlled by temperature. Effective burial stress is caused by the weight of all overlying water...... and sediments as counteracted by the pressure in the pore fluid, so the regional overpressure in the Central North Sea is one reason why the two localities have different relationships between temperature and effective burial stress. In the chalk of the Ontong Java Plateau the onset of calcite-silicate pressure...... equilibrated to quartz before the onset of pressure dissolution and thus, in this case, dissolution and precipitation of calcite have no lag. This temperature versus effective burial stress induced difference in diagenetic history is of particular relevance when exploring for hydrocarbons in normally pressured...

  14. Tribological properties of silicate materials on nano and microscale

    Energy Technology Data Exchange (ETDEWEB)

    Tordjeman, Ph., E-mail: [Universite de Toulouse-CNRS, Institut de Mecanique des Fluides de Toulouse UMR 5502, Allee Camille Soula, F-31400 Toulouse (France); Morel, N. [Laboratoire IES, Groupe Micro et RheoAcoustique, UMR CNRS 5214, Universite Montpellier 2, CC 082, Pl. E. Bataillon, 34095 Montpellier Cedex 05 (France); Ramonda, M. [Laboratoire de Microscopie a Champ Proche, LMCP, Universite Montpellier 2, CC 082, Pl. E. Bataillon, 34095 Montpellier Cedex 05 (France)


    We studied the friction properties of four model silicate materials at the nanoscale and microscale. From nanotribology, we characterized the tribological properties at single asperity contact scale and from microtribology, we characterized the tribological properties at multi asperity contact scale. First, for each material we measured chemical composition by XPS, Young's modulus by acoustical microscopy and roughness {sigma} by atomic force microscopy (AFM). Second, we measured the nanofriction coefficients with an AFM and the microfriction coefficients with a ball probe tribometer, for three hardnesses of the ball probe. We identified one friction mechanism at the nanoscale (sliding friction) and two friction mechanisms at the microscale (sliding friction and yielding friction). Comparison of the nano and microfriction coefficients at the same sliding friction regime shown, that the tribological properties of these materials didn't depend on roughness.

  15. High-dose dosimetry using natural silicate minerals

    Energy Technology Data Exchange (ETDEWEB)

    Carmo, Lucas S. do; Mendes, Leticia, E-mail: [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Watanabe, Shigueo; Rao, Gundu; Lucas, Natasha; Sato, Karina, E-mail: [Universidade de Sao Paulo (USP), Sao Paulo, SP (Brazil). Instituto de Fisica. Departamento de Fisica Nuclear; Barbosa, Renata F., E-mail: [Universidade Federal de Sao Paulo (UNIFESP), Santos, SP (Brazil). Departamento de Ciencias do Mar


    In the present study, certain natural silicate minerals such as aquamarine (AB), morganite (PB), goshenite (WB), white jadeite (JW), green jadeite (JG), pink tourmaline (PT) and two varieties of jadeite-like quartz, denoted here by JQ1 and JQ2, were investigated using the thermoluminescence technique to evaluate their potential for use as very-high- and high-dose dosimeters. These minerals respond to high doses of γ-rays of up to 1000 kGy and often to very high doses of up to 3000 kGy. The TL response of these minerals may be considered to be satisfactory for applications in high-dose dosimetry. Investigations of electron paramagnetic resonance and optically stimulated luminescence dosimetry are in progress. (author)

  16. Luminescent solar concentrators using uranyl-doped silicate glasses (United States)

    Folcher, G.; Keller, N.; Paris, J.


    The effect of the uranium concentration on the performance of uranyl-doped glass used in solar concentrators was examined experimentally. Na-Ca silicate glass and UO3 additive were prepared at 1250 C, cooled to 600 C, annealed at 700 C, and cooled to ambient for the tests. Light absorption was proportional to uranium content up to a 2 percent concentration. A doped-glass test cell filled with a fluoresceine solution and irradiated at 337 nm and 420 nm with laser light was monitored to measure the luminescent lifetimes of the uranyl ions. A 380 microsec half-lifetime was determined, along with a quantum yield that varied from 0.5 at 1 percent uranyl concentration to 0.3 at a 5 percent concentration. The quantum efficiencies could be attained with 1 cm thick glass with existing manufacturing technologies, and thinner glass with further developments.

  17. Trace element partitioning between plagioclase and silicate melt: The importance of temperature and plagioclase composition, with implications for terrestrial and lunar magmatism (United States)

    Sun, Chenguang; Graff, Michelle; Liang, Yan


    Trace element partition coefficients between anorthitic plagioclase and basaltic melts (D) have been determined experimentally at 0.6 GPa and 1350-1400 °C in a lunar high-Ti picritic glass and a mid-ocean ridge basalt (MORB). Plagioclases with 98 mol% and 86 mol% anorthite were produced in the lunar picritic melt and MORB melt, respectively. Based on the new experimental partitioning data and those selected from the literature, we developed parameterized lattice strain models for the partitioning of monovalent (Na, K, Li), divalent (Ca, Mg, Ba, Sr, Ra) and trivalent (REE and Y) cations between plagioclase and silicate melt. Through the new models we showed that the partitioning of these trace elements in plagioclase depends on temperature, pressure, and the abundances of Ca and Na in plagioclase. Particularly, Na content in plagioclase primarily controls divalent element partitioning, while temperature and Ca content in plagioclase are the dominant factors for REE partitioning in plagioclase. From these models, we also derived a new expression for DRa/DBa that can be used for Ra-Th dating on volcanic plagioclase phenocrysts, and a new model for plagioclase-melt noble gas partitioning. Applications of these partitioning models to fractional crystallization of MORB and lunar magma ocean (LMO) indicate that (1) the competing effect of temperature and plagioclase composition leads to small variations of plagioclase-melt DREE during MORB differentiation, but (2) the temperature effect is especially significant and can vary anorthite-melt DREE by over one order of magnitude during LMO solidification. Temperature and plagioclase composition have to be considered when modeling the chemical differentiation of mafic to felsic magmas involving plagioclase.

  18. Variation of olivine composition in the volcanic rocks in the Songliao basin, NE China: lithosphere control on the origin of the K-rich intraplate mafic lavas (United States)

    Zhang, L.-Y.; Prelević, D.; Li, N.; Mertz-Kraus, R.; Buhre, S.


    Lithospheric thickness and the heterogeneity of the mantle lithosphere are two major parameters that play a role in determining the final composition of the mafic melts and their minerals. The Songliao basin in northeast China represents an ideal natural laboratory to study the effect of these two parameters on early Pliocene to Holocene K-rich mafic lavas (K2O > 4 wt.%; K2O/Na2O > 1). A series of Cenozoic volcanic edifices (Erkeshan, Wudalianchi, Keluo and Xiaogulihe) are tentatively divided into three groups (Group 1 - thin, Group 2 - middle, and Group 3 - thick) according to the lithosphere thickness. They are located in the northern region of the Songliao basin extending in a near north-south direction along a broad zone where the lithosphere thickness increases gradually. We present a detailed petrographical and geochemical study on olivine macrocrysts in combination with new geochemical data on their host lavas, including major and trace element abundances as well as Sr, Nd, and Pb isotopic signatures. Our ultimate aim is to quantitatively and qualitatively determine the role of lithospheric mantle thickness (named as ;lid effect;) and composition in the variation of mafic lavas and olivine composition. When corrected to Mg# = 0.72, a number of major elements in the lavas correlate with increasing lithospheric thickness (L): Si72 and Al72 decrease, whereas Mg72, Fe72, Ti72 and P72 increase. Sm/Yb ratios in the lavas increase, implying that lithospheric thickness exerts an important control. Group 3 mafic lavas are ultrapotassic (showing lamproite affinity) with K2O/Na2O > 4: their La/Sm and Pb isotope ratios deviate from the above correlations, indicating that the lavas from the thickest part of the basin exhibit the highest extent of metasomatic enrichment of the mantle source. Several parameters (e.g. [Ni], Ni/Mg, Ni/(Mg/Fe), Mn/Fe and Ca/Fe) in melt-related olivine from Group 1 and Group 2 lavas are controlled by variable lithosphere thickness. Olivine

  19. A-thermal elastic behavior of silicate glasses (United States)

    Rabia, Mohammed Kamel; Degioanni, Simon; Martinet, Christine; Le Brusq, Jacques; Champagnon, Bernard; Vouagner, Dominique


    Depending on the composition of silicate glasses, their elastic moduli can increase or decrease as function of the temperature. Studying the Brillouin frequency shift of these glasses versus temperature allows the a-thermal composition corresponding to an intermediate glass to be determined. In an intermediate glass, the elastic moduli are independent of the temperature over a large temperature range. For sodium alumino-silicate glasses, the a-thermal composition is close to the albite glass (NaAlSi3O8). The structural origin of this property is studied by in situ high temperature Raman scattering. The structure of the intermediate albite glass and of silica are compared at different temperatures between room temperature and 600 °C. When the temperature increases, it is shown that the high frequency shift of the main band at 440 cm-1 in silica is a consequence of the cristobalite-like alpha-beta transformation of 6-membered rings. This effect is stronger in silica than bond elongation (anharmonic effects). As a consequence, the elastic moduli of silica increase as the temperature increases. In the albite glass, the substitution of 25% of Si4+ ions by Al3+ and Na+ ions decreases the proportion of SiO2 6-membered rings responsible for the silica anomaly. The effects of the silica anomaly balance the anharmonicity in albite glass and give rise to an intermediate a-thermal glass. Different networks, formers or modifiers, can be added to produce different a-thermal glasses with useful mechanical or chemical properties.

  20. Evaluation of apatite silicates as solid oxide fuel cell electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Marrero-Lopez, D. [Dpto. de Fisica Aplicada I, Laboratorio de Materiales y Superficies (Unidad Asociada al C.S.I.C.), Universidad de Malaga, 29071 Malaga (Spain); Dpto. de Quimica Inorganica, Universidad de La Laguna, 38200 La Laguna, Tenerife (Spain); Martin-Sedeno, M.C.; Aranda, M.A.G. [Dpto. de Quimica Inorganica, Universidad Malaga, 29071 Malaga (Spain); Pena-Martinez, J. [Dpto. de Quimica Inorganica, Universidad de La Laguna, 38200 La Laguna, Tenerife (Spain); Instituto de Energias Renovables, Parque Tecnologico, Universidad de Castilla La Mancha, 02006 Albacete (Spain); Ruiz-Morales, J.C.; Nunez, P. [Dpto. de Quimica Inorganica, Universidad de La Laguna, 38200 La Laguna, Tenerife (Spain); Ramos-Barrado, J.R. [Dpto. de Fisica Aplicada I, Laboratorio de Materiales y Superficies (Unidad Asociada al C.S.I.C.), Universidad de Malaga, 29071 Malaga (Spain)


    Apatite-type silicates have been considered as promising electrolytes for Solid Oxide Fuel Cells (SOFC); however studies on the potential use of these materials in SOFC devices have received relatively little attention. The lanthanum silicate with composition La{sub 10}Si{sub 5.5}Al{sub 0.5}O{sub 26.75} has been evaluated as electrolyte with the electrode materials commonly used in SOFC, i.e. manganite, ferrite and cobaltite as cathode materials and NiO-CGO composite, chromium-manganite and Sr{sub 2}MgMoO{sub 6} as anode materials. Chemical compatibility, area-specific resistance and fuel cell studies have been performed. X-ray powder diffraction (XRPD) analysis did not reveal any trace of reaction products between the apatite electrolyte and most of the aforementioned electrode materials. However, the area-specific polarisation resistance (ASR) of these electrodes in contact with apatite electrolyte increased significantly with the sintering temperature, indicating reactivity at the electrolyte/electrode interface. On the other hand, the ASR values are significantly improved using a ceria buffer layer between the electrolyte and electrode materials to prevent reactivity. Maximum power densities of 195 and 65 mWcm{sup -2} were obtained at 850 and 700 C, respectively in H{sub 2} fuel, using an 1 mm-thick electrolyte, a NiO-Ce{sub 0.8}Gd{sub 0.2}O{sub 1.9} composite as anode and La{sub 0.6}Sr{sub 0.4}Co{sub 0.8}Fe{sub 0.2}O{sub 3-{delta}} as cathode materials. This fuel cell was tested for 100 h in 5%H{sub 2}-Ar atmosphere showing stable performance. (author)

  1. Low Velocity Sphere Impact of a Soda Lime Silicate Glass

    Energy Technology Data Exchange (ETDEWEB)

    Wereszczak, Andrew A [ORNL; Fox, Ethan E [ORNL; Morrissey, Timothy G [ORNL; Vuono, Daniel J [ORNL


    This report summarizes TARDEC-sponsored work at Oak Ridge National Laboratory (ORNL) during the FY11 involving low velocity (< 30 m/s or < 65 mph) ball impact testing of Starphire soda lime silicate glass. The intent was to better understand low velocity impact response in the Starphire for sphere densities that bracketed that of rock. Five sphere materials were used: borosilicate glass, soda-lime silicate glass, steel, silicon nitride, and alumina. A gas gun was fabricated to produce controlled velocity delivery of the spheres against Starphire tile targets. Minimum impact velocities to initiate fracture in the Starphire were measured and interpreted in context to the kinetic energy of impact and the elastic property mismatch between the any of the five sphere-Starphire-target combinations. The primary observations from this low velocity (< 30 m/s or < 65 mph) testing were: (1) Frictional effects contribute to fracture initiation. (2) Spheres with a lower elastic modulus require less force to initiate fracture in the Starphire than spheres with a higher elastic modulus. (3) Contact-induced fracture did not initiate in the Starphire SLS for impact kinetic energies < 150 mJ. Fracture sometimes initiated or kinetic energies between {approx} 150-1100 mJ; however, it tended to occur when lower elastic modulus spheres were impacting it. Contact-induced fracture would always occur for impact energies > 1100 mJ. (4) The force necessary to initiate contact-induced fracture is higher under dynamic or impact conditions than it is under quasi-static indentation conditions. (5) Among the five used sphere materials, silicon nitride was the closest match to 'rock' in terms of both density and (probably) elastic modulus.

  2. In vitro cytotoxicity of calcium silicate-containing endodontic sealers. (United States)

    Zhou, Hui-min; Du, Tian-feng; Shen, Ya; Wang, Zhe-jun; Zheng, Yu-feng; Haapasalo, Markus


    The cytotoxicity of 2 novel calcium silicate-containing endodontic sealers to human gingival fibroblasts was studied. EndoSequence BC (Brasseler, Savannah, GA), MTA Fillapex (Angelus Indústria de Produtos Odontológicos S/A, Londrina, PR, Brazil) and a control sealer (AH Plus; Dentsply DeTrey GmbH, Konstanz, Germany) were evaluated. Human gingival fibroblasts were incubated for 3 days both with the extracts from fresh and set materials in culture medium and cultured on the surface of the set materials in Dulbecco-modified Eagle medium. Fibroblasts cultured in Dulbecco-modified Eagle medium were used as a control group. Cytotoxicity was evaluated by flow cytometry, and the adhesion of the fibroblasts to the surface of the set materials was assessed using scanning electron microscopy. The data of cell cytotoxicity were analyzed statistically using a 1-way analysis of variance test at a significance level of P extracts from BC Sealer showed higher viabilities at all extract concentrations than cells incubated with extracts from freshly mixed AH Plus and fresh and set MTA Fillapex, esspecially for the high extract concentrations (1:2 and 1:8 dilutions). Extracts from set MTA Fillapex of 2 weeks and older were more cytotoxic than extracts from freshly mixed and 1-week-old cement. With extract concentrations of 1:32 and lower, MTA Fillapex was no longer cytotoxic. After setting, AH Plus was no longer cytotoxic, and the fibroblast cells grew on set AH Plus equally as well as on BC Sealer. BC Sealer and MTA Fillapex, the 2 calcium silicate-containing endodontic sealers, exhibited different cytotoxicity to human gingival fibroblasts. Copyright © 2015 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  3. Modified tricalcium silicate cement formulations with added zirconium oxide. (United States)

    Li, Xin; Yoshihara, Kumiko; De Munck, Jan; Cokic, Stevan; Pongprueksa, Pong; Putzeys, Eveline; Pedano, Mariano; Chen, Zhi; Van Landuyt, Kirsten; Van Meerbeek, Bart


    This study aims to investigate the effect of modifying tricalcium silicate (TCS) cements on three key properties by adding ZrO 2 . TCS powders were prepared by adding ZrO 2 at six different concentrations. The powders were mixed with 1 M CaCl 2 solution at a 3:1 weight ratio. Biodentine (contains 5 wt.% ZrO 2 ) served as control. To evaluate the potential effect on mechanical properties, the mini-fracture toughness (mini-FT) was measured. Regarding bioactivity, Ca release was assessed using ICP-AES. The component distribution within the cement matrix was evaluated by Feg-SEM/EPMA. Cytotoxicity was assessed using an XTT assay. Adding ZrO 2 to TCS did not alter the mini-FT (p = 0.52), which remained in range of that of Biodentine (p = 0.31). Ca release from TSC cements was slightly lower than that from Biodentine at 1 day (p > 0.05). After 1 week, Ca release from TCS 30 and TCS 50 increased to a level that was significantly higher than that from Biodentine (p  0.05). EPMA revealed a more even distribution of ZrO 2 within the TCS cements. Particles with an un-reacted core were surrounded by a hydration zone. The 24-, 48-, and 72-h extracts of TCS 50 were the least cytotoxic. ZrO 2 can be added to TCS without affecting the mini-FT; Ca release was reduced initially, to reach a prolonged release thereafter; adding ZrO 2 made TCS cements more biocompatible. TCS 50 is a promising cement formulation to serve as a biocompatible hydraulic calcium silicate cement.

  4. A carbonate-silicate aqueous geochemical cycle model for Mars (United States)

    Schaefer, M. W.; Leidecker, H.


    A model for the carbonate-silicate geochemical cycle of an early, wet Mars is under development. The results of this study will be used to constrain models of the geochemical history of Mars and the likely mineralogy of its present surface. Although Mars today is a cold, dry planet, it may once have been much warmer and wetter. Values of total outgassed CO2 from several to about 10 bars are consistent with present knowledge (Pollack et al. 1987), and this amount of CO2 implies an amount of water outgassed at least equal to an equivalent depth of 500-1000 meters (Carr 1986). Pollack et al. (1987), in addition, estimate that a thick CO2 atmosphere may have existed for an extended period of time, perhaps as long as a billion years. The greenhouse effect of such an atmosphere would permit the presence of liquid water on the surface, most likely in the form of a shallow sea in the lowest regions of the planet, such as the northern plains (Schaefer 1990). The treatment of geochemical cycles as complex kinetic chemical reactions has been undertaken for terrestrial systems in recent years with much success (Lasaga 1980, 1981; Berner et al. 1983; Lasaga et al. 1985). Although the Martian system is vastly less well understood, and hence less well-constrained, it is also a much simpler system, due to the lack of biogenic reactions that make the terrestrial system so complex. It should be possible, therefore, to use the same techniques to model the Martian system as have been used for terrestrial systems, and to produce useful results. A diagram of the carbonate-silicate cycle for Mars (simplified from the terrestrial system) is given.

  5. Fluorine in silicate glasses: A multinuclear nuclear magnetic resonance study

    Energy Technology Data Exchange (ETDEWEB)

    Schaller, T.; Dingwell, D.B.; Keppler, H.; Merwin, L.; Sebald, A. (Univ. Bayreuth (West Germany)); Knoeller, W. (Bruker Analytische Messtechnik, Rheinstetten (West Germany))


    Anhydrous nepheline, jadeite, and albite glasses doped with F as well as hydrous F-containing haplogranitic glasses were investigated using {sup 19}F combined rotation and multiple-pulse spectroscopy; {sup 19}F {yields} {sup 29}Si cross-polarization/magic angle spinning (MAS); and high-power {sup 19}F decoupled {sup 29}Si, {sup 23}Na, and {sup 27}Al MAS nuclear magnetic resonance methods. Fluorine preferentially coordinates with Al to form octahedral AlF{sub 6}{sup 3{minus}} complexes in all glasses studied. In addition, F anions bridging two Al cations, units containing octahedral Al coordinated by both O and F, or tetrahedral Al-F complexes might be present. The presence of Si-F bonds cannot be entirely ruled out but appears unlikely on the basis of the {sup 19}F {yields} {sup 29}Si CP/MAS spectra. There is no evidence for any significant coordination of F with alkalis in the glasses studied. Over the range of F contents studied (up to 5 wt.%), there seems to be hardly any dependence of F speciation on the concentration of F in the samples. The spectroscopic results explain the decrease of the viscosity of silicate melts with increasing F content by removal of Al from bridging AlO{sub 4}-units due to complexing with F, which causes depolymerization of the melt. The same mechanism can account for the shift of the eutectic point in the haplogranite system to more feldspar-rich compositions with increasing F content, and for the peraluminous composition of most F-rich granites. Liquid immiscibility in F-rich granitic melts might be caused by formation of (Na,K){sub 3}AlF{sub 6} units in the melt with little or no interaction with the silicate component. The presence of F in granitic melts might increase the solubility of high field strength cations by making nonbridging O atoms available which form complexes with these cations.

  6. Relationships between CO2, thermodynamic limits on silicate weathering, and the strength of the silicate weathering feedback (United States)

    Winnick, Matthew J.; Maher, Kate


    Recent studies have suggested that thermodynamic limitations on chemical weathering rates exert a first-order control on riverine solute fluxes and by extension, global chemical weathering rates. As such, these limitations may play a prominent role in the regulation of carbon dioxide levels (pCO2) over geologic timescales by constraining the maximum global weathering flux. In this study, we develop a theoretical scaling relationship between equilibrium solute concentrations and pCO2 based on equilibrium constants and reaction stoichiometry relating primary mineral dissolution and secondary mineral precipitation. We test this theoretical scaling relationship against reactive transport simulations of chemical weathering profiles under open- and closed-system conditions, representing partially and fully water-saturated regolith, respectively. Under open-system conditions, equilibrium bicarbonate concentrations vary as a power-law function of pCO2 (y = kxn) where n is dependent on reaction stoichiometry and k is dependent on both reaction stoichiometry and the equilibrium constant. Under closed-system conditions, bicarbonate concentrations vary linearly with pCO2 at low values and approach open-system scaling at high pCO2. To describe the potential role of thermodynamic limitations in the global silicate weathering feedback, we develop a new mathematical framework to assess weathering feedback strength in terms of both (1) steady-state atmospheric pCO2 concentrations, and (2) susceptibility to secular changes in degassing rates and transient carbon cycle perturbations, which we term 1st and 2nd order feedback strength, respectively. Finally, we discuss the implications of these results for the effects of vascular land plant evolution on feedback strength, the potential role of vegetation in controlling modern solute fluxes, and the application of these frameworks to a more complete functional description of the silicate weathering feedback. Most notably, the dependence

  7. A design of spectrophotometric microfluidic chip sensor for analyzing silicate in seawater (United States)

    Cao, X.; Zhang, S. W.; Chu, D. Z.; Wu, N.; Ma, H. K.; Liu, Y.


    High quality and continuous in situ silicate data are required to investigate the mechanism of the biogeochemical cycles and the formation of red tide. There is an urgently growing need for autonomous in situ silicate instruments that perform determination on various platforms. However, due to the high reagents and power consumption, as well as high system complexity leading to low reliability and robustness, the performance of the commercially available silicate sensors is not satisfactory. With these problems, here we present a new generation of microfluidic continuous flow analysis silicate sensor with sufficient analytical performance and robustness, for in situ determination of soluble silicate in seawater. The reaction mechanism of this sensor is based on the reaction of silicate with ammonium molybdate to form a yellow silicomolybdate complex and further reduction to silicomoIybdenum blue by ascorbic acid. The minimum limit of detection was 45.1 nmol L-1, and the linear determination range of the sensor is 0-400 μmol L-1. The recovery rate of the actual water is between 98.1%-104.0%, and the analyzing cycle of the sensor is about 5 minutes. This sensor has the advantages of high accuracy, high integration, low water consumption, and strong anti-interference ability. It has been successfully applied to measuring the silicate in seawater in Jiaozhou Bay.

  8. Petrophysical Analysis of Siliceous-Ooze Sediments, More Basin, Norwegian Sea

    DEFF Research Database (Denmark)

    Awedalkarim, Ahmed; Sørensen, Morten Kanne; Fabricius, Ida Lykke


    Pelagic siliceous-ooze sediments occur above the hydrocarbon reservoir of the Ormen Lange gas field in More Basin, Norwegian Sea. A possible hydrocarbon prospect of siliceous ooze was proposed, but siliceous ooze is significantly different in texture from most commonly known reservoir rocks. Logg....... Amplitude-versus-offset analysis indicated that an oil-saturated sandstone layer can be distinguished from water-saturated siliceous ooze.......Pelagic siliceous-ooze sediments occur above the hydrocarbon reservoir of the Ormen Lange gas field in More Basin, Norwegian Sea. A possible hydrocarbon prospect of siliceous ooze was proposed, but siliceous ooze is significantly different in texture from most commonly known reservoir rocks...... was calculated from the gamma-ray log and empirical grain-density data were calibrated with X-ray diffraction analysis data. The grain-density log was used with the calculated true porosity log and the brine density of 1.025 g/cm(3) to convert the bulk-density log from conventional limestone and water scaling...

  9. Evaluation of the effect of sodium silicate addition to mine backfill, Gelfill − Part 1

    Directory of Open Access Journals (Sweden)

    M. Kermani


    Full Text Available In this paper, the mechanical properties of sodium silicate-fortified backfill, called Gelfill, were investigated by conducting a series of laboratory experiments. Two configurations were tested, i.e. Gelfill and cemented hydraulic fill (CHF. The Gelfill has an alkali activator such as sodium silicate in its materials in addition to primary materials of mine backfill which are tailings, water and binders. Large numbers of samples of Gelfill and CHF with various mixture designs were cast and cured for over 28 d. The mechanical properties of samples were investigated using uniaxial compression test, and the results were compared with those of reference samples made without sodium silicate. The test results indicated that the addition of an appropriate amount of an alkali activator such as sodium silicate can enhance the mechanical (uniaxial compressive strength and physical (water retention properties of backfill. The microstructure analysis conducted by mercury intrusion porosimetry (MIP revealed that the addition of sodium silicate can modify the pore size distribution and total porosity of Gelfill, which can contribute to the better mechanical properties of Gelfill. It was also shown that the time and rate of drainage in the Gelfill specimens are less than those in CHF specimens made without sodium silicate. Finally, the study showed that the addition of sodium silicate can reduce the required setting time of mine backfill, which can contribute to increase mine production in accordance with the mine safety.

  10. Bilateral urinary calculi after treatment with a silicate-containing milk thickener. (United States)

    Ulinski, Tim; Sabot, Jean-François; Bourlon, Isabelle; Cochat, Pierre


    Nephrocalcinosis and/or urinary calculi are rare in infants. Furosemide treatment during the neonatal period, vitamin D intoxication, hereditary diseases such as hyperoxaluria or distal tubular acidosis are among the most common aetiologies. We report the case of a 6-month-old boy with an extra-hepatic biliary duct atresia treated by the Kasai procedure and a gastro-oesophageal reflux treated with a silicate containing milk thickener (Gelopectose, 5.5% colloidal silicate) since the neonatal period. He did not present any other endogenous risk factor for urinary stone formation (normal urinary calcium/creatinine ratio; normal urinary magnesium excretion). The nephrolithiasis was discovered as the boy presented painful episodes of macroscopic haematuria. Ultrasound examination revealed bilateral nephrocalcinosis and multiple bilateral calculi without infection or urinary obstruction. Infrared spectroscopy revealed silicate as the major component suggesting silicate absorption to be responsible for the described symptoms. After replacement of the silicate-containing agent by a silicate-free milk thickener, the lesions were completely reversible as confirmed by repeated renal ultrasound examinations over a 2-month period. Silicate-containing milk thickeners can be responsible for urinary calculi and/or nephrocalcinosis.

  11. Petrological and geochemical constraints on the origin of mafic dykes intruding the composite Kaçkar Pluton from the eastern Blacksea magmatic arc, NE Turkey (United States)

    Aydin, Faruk; Oguz, Simge; Baser, Rasim; Uysal, Ibrahim; Sen, Cüneyt; Karsli, Orhan; Kandemir, Raif


    Geological, petrographical and geochemical data of mafic dykes intruding the composite Kaçkar Pluton from the eastern Blacksea magmatic arc (EBMA), NE Turkey, provide new insights into the nature of the metasomatizing agents in subcontinental lithospheric mantle beneath the region during the late Mesozoic-early Tertiary. Mafic dykes from the Çaykara and Hayrat (Trabzon), and also Ikizdere (Rize) areas from the northern margin of the EBMA consist of basalts, dolerites, lamprophyres (basic member) and lesser basaltic andesites and trachyandesites (evolved member). All dykes have no deformation and metamorphism. The outcrops of these dykes vary, with thickness from 0.2 to 10 m. and visible length from 3 to 20 m. In general, the mafic dykes dip steeply and cut directly across the Kaçkar Pluton, and show NW- and NE-trending, roughly parallel to the orientations of the EBMA main faults. Most of the dyke samples display subaphyric to porphyritic texture with phenocrysts of plagioclase (up to 10%), clinopyroxene (5-20%), amphibole (5-15%), and some contain variable amount of biotite (5-20%), lesser quartz (1-2%), and minor euhedral zircon, apatite and Fe-Ti oxides. The basic members of the mafic dykes have SiO2 of 44.1-51.9%, MgO of 4.5-12.1%, and TiO2 >mostly 0.8% (up to 2.3%) with K2O+Na2O of 1.3-6.6% with mostly subalkaline character. They are relatively high in mg-number (0.45-0.73) and transition metals (V=171-376 ppm, Co=22-45 ppm, Ni=3-148 ppm, and Sc=21-49 ppm). The evolved members of the dykes exhibit relatively higher SiO2 (57.1-60.2%) and K2O+Na2O (5.6-9.0%), and lower MgO (2.2-5.9%) and TiO2 (0.5-0.8%) contents than those from the basic dykes. Also, these samples have slightly low mg-number (0.41-0.65) and transition metals (V=99-172 ppm, Co=9-22 ppm, Ni=1-43 ppm, and Sc=9-20 ppm). In the Harker diagrams, all samples of the mafic dykes form a continuous array, and exhibit similar geochemical characteristics. In general, SiO2 inversely correlates with MgO, Fe

  12. Preparation and Characterization of Lithium Zirconium Silicate for CO2 Capture

    Directory of Open Access Journals (Sweden)

    T.S. Bhosale


    Full Text Available The samples of lithium zirconium silicate were prepared by precipitation, template and sol-gel meth-ods. The samples were prepared with several mol ratios of Li:Zr:Si. The preparation of lithium zirco-nium silicate samples by precipitation method were carried out by using the lithium nitrate, zirconyl nitrate, zirconium(IV oxypropoxide and tetramethylorthosilicate (TEOS as precursors. The samples of lithium zirconium silicate were prepared by using cetyltrimethyl-ammonium bromide (C-TAB and tetramethyl ammonium hydroxide (TMAOH by template method. The samples of lithium zirconium silicate were characterized by XRD, TEM, SEM, 29Si-MAS NMR and FTIR. The surface area, alkalinity / acidity of the samples of lithium zirconium silicate were measured. The TGA analysis of lithium zirco-nium silicate samples was done. The CO2 captured by the samples of lithium zirconium silicate was es-timated. The captured CO2 by the samples of lithium zirconium silicate was found to be in the range 3.3 to 8.6 wt%. © 2014 BCREC UNDIP. All rights reservedReceived: 27th March 2014; Revised: 31st July 2014; Accepted: 2nd August 2014How to Cite: Bhosale, T.S. , Gaikwad, A.G. (2014. Preparation and Characterization of Lithium Zirconium Silicate for CO2 Capture. Bulletin of Chemical Reaction Engineering & Catalysis, 9(3: 249-262. (doi:10.9767/bcrec.9.3.6646.249-262Permalink/DOI:

  13. Sulfur Saturation Limits in Silicate Melts and their Implications for Core Formation Scenarios for Terrestrial Planets (United States)

    Holzheid, Astrid; Grove, Timothy L.


    This study explores the controls of temperature, pressure, and silicate melt composition on S solubility in silicate liquids. The solubility of S in FeO-containing silicate melts in equilibrium with metal sulfide increases significantly with increasing temperature but decreases with increasing pressure. The silicate melt structure also exercises a control on S solubility. Increasing the degree of polymerization of the silicate melt structure lowers the S solubility in the silicate liquid. The new set of experimental data is used to expand the model of Mavrogenes and O'Neill(1999) for S solubility in silicate liquids by incorporating the influence of the silicate melt structure. The expected S solubility in the ascending magma is calculated using the expanded model. Because the negative pressure dependence of S solubility is more influential than the positive temperature dependence, decompression and adiabatic ascent of a formerly S-saturated silicate magma will lead to S undersaturation. A primitive magma that is S-saturated in its source region will, therefore, become S-undersaturated as it ascends to shallower depth. In order to precipitate magmatic sulfides, the magma must first cool and undergo fractional crystallization to reach S saturation. The S content in a metallic liquid that is in equilibrium with a magma ocean that contains approx. 200 ppm S (i.e., Earth's bulk mantle S content) ranges from 5.5 to 12 wt% S. This range of S values encompasses the amount of S (9 to 12 wt%) that would be present in the outer core if S is the light element. Thus, the Earth's proto-mantle could be in equilibrium (in terms of the preserved S abundance) with a core-forming metallic phase.

  14. A model of sulphur solubility for hydrous mafic melts: application to the determination of magmatic fluid compositions of Italian volcanoes

    Directory of Open Access Journals (Sweden)

    M. Pichavant


    Full Text Available We present an empirical model of sulphur solubility that allows us to calculate f S2 if P, T, fO2 and the melt composition, including H2O and S, are known. The model is calibrated against three main experimental data bases consisting in both dry and hydrous silicate melts. Its prime goal is to calculate the f S2 of hydrous basalts that currently lack experimental constraints of their sulphur solubility behaviour. Application of the model to Stromboli, Vesuvius, Vulcano and Etna eruptive products shows that the primitive magmas found at these volcanoes record f S2 in the range 0.1-1 bar. In contrast, at all volcanoes the magmatic evolution is marked by dramatic variations in f S2 that spreads over up to 9 orders of magnitude. The f S2 can either increase during differentiation or decrease during decompression to shallow reservoirs, and seems to be related to closed versus open conduit conditions, respectively. The calculated f S2 shows that the Italian magmas are undersaturated in a FeS melt, except during closed conduit conditions, in which case differentiation may eventually reach conditions of sulphide melt saturation. The knowledge of f S2, fO2 and fH2O allows us to calculate the fluid phase composition coexisting with magmas at depth in the C-O-H-S system. Calculated fluids show a wide range in composition, with CO2 mole fractions of up to 0.97. Except at shallow levels, the fluid phase is generally dominated by CO2 and H2O species, the mole fractions of SO2 and H2S rarely exceeding 0.05 each. The comparison between calculated fluid compositions and volcanic gases shows that such an approach should provide constraints on both the depth and mode of degassing, as well as on the amount of free fluid in magma reservoirs. Under the assumption of a single step separation of the gas phase in a closed-system condition, the application to Stromboli and Etna suggests that the main reservoirs feeding the eruptions and persistent

  15. Pockels effect of silicate glass-ceramics: Observation of optical modulation in Mach-Zehnder system. (United States)

    Yamaoka, Kazuki; Takahashi, Yoshihiro; Yamazaki, Yoshiki; Terakado, Nobuaki; Miyazaki, Takamichi; Fujiwara, Takumi


    Silicate glass has been used for long time because of its advantages from material's viewpoint. In this paper, we report the observation of Pockels effect by Mach-Zehnder interferometer in polycrystalline ceramics made from a ternary silicate glass via crystallization due to heat-treatment, i.e., glass-ceramics. Since the silicate system is employed as the precursor, merits of glass material are fully utilized to fabricate the optical device component, in addition to that of functional crystalline material, leading us to provide an electro-optic device, which is introducible into glass-fiber network.


    Directory of Open Access Journals (Sweden)

    V. U. Matsapulin


    Full Text Available The article analyzes the resource base, reserves and the use of siliceous rocks, their economic feasibility of the use for production of building materials of new generation with low-energy and other costs. Presented are the results of laboratory research and testing technology of production of insulating foam from a composition based on an aqueous solution of sodium silicate obtained from the local siliceous rocks (diatomite and the liquid alkali component - soapstock, hardener from ferrochrome slag and waste carbonate rock able to harden at a low temperature processing ( 100-110 ° C.

  17. Production of reactive oxygen species from abraded silicates. Implications for the reactivity of the Martian soil

    DEFF Research Database (Denmark)

    Bak, Ebbe Norskov; Zafirov, Kaloyan; Merrison, Jonathan P.


    to oxidants in the form of hydrogen peroxide (H2O2) and hydroxyl radicals (⋅OH). We found that silicate samples abraded in simulated Martian atmospheres gave rise to a significant production of H2O2 and ⋅OH upon contact with water. Our experiments demonstrated that abraded silicates could lead to a production...... of H2O2 facilitated by atmospheric O2 and inhibited by carbon dioxide. Furthermore, during simulated saltation the silicate particles became triboelectrically charged and at pressures similar to the Martian surface pressure we observed glow discharges. Electrical discharges can cause dissociation of CO...

  18. Carbonate formation in non-aqueous environments by solid-gas carbonation of silicates (United States)

    Day, S. J.; Thompson, S. P.; Evans, A.; Parker, J. E.


    We have produced synthetic analogues of cosmic silicates using the Sol Gel method, producing amorphous silicates of composition Mg(x)Ca(1-x)SiO3. Using synchrotron X-ray powder diffraction on Beamline I11 at the Diamond Light Source, together with a newly-commissioned gas cell, real-time powder diffraction scans have been taken of a range of silicates exposed to CO2 under non-ambient conditions. The SXPD is complemented by other techniques including Raman and Infrared Spectroscopy and SEM imaging.

  19. The distribution of chromium among orthopyroxene, spinel and silicate liquid at atmospheric pressure (United States)

    Barnes, S. J.


    The Cr distributions for a synthetic silicate melt equilibrated with bronzitic orthopyroxene and chromite spinel between 1334 and 1151 C over a range of oxygen fugacities between the nickel-nickel oxide and iron-wuestite buffers are studied. The occurrence, chemical composition, and structure of the orthopyroxene-silicate melt and the spinel-silicate melt are described. It is observed that the Cr content between bronzite and the melt increases with falling temperature along a given oxygen buffer and decreases with falling oxygen fugacity at a given temperature; however, the Cr content of the melt in equilibrium with spinel decreases with falling temperature and increases with lower oxygen fugacity.

  20. Integrated elemental and Sr-Nd-Pb-Hf isotopic studies of Mesozoic mafic dykes from the eastern North China Craton: implications for the dramatic transformation of lithospheric mantle (United States)

    Liu, Shen; Feng, Caixia; Santosh, M.; Feng, Guangying; Coulson, Ian M.; Xu, Mengjing; Guo, Zhuang; Guo, Xiaolei; Peng, Hao; Feng, Qiang


    Evolution of the lithospheric mantle beneath the North China Craton (NCC) from its Precambrian cratonic architecture until Paleozoic, and the transformation to an oceanic realm during Mesozoic, with implications on the destruction of cratonic root have attracted global attention. Here we present geochemical and isotopic data on a suite of newly identified Mesozoic mafic dyke swarms from the Longwangmiao, Weijiazhuang, Mengjiazhuang, Jiayou, Huangmi, and Xiahonghe areas (Qianhuai Block) along the eastern NCC with an attempt to gain further insights on the lithospheric evolution of the region. The Longwangmiao dykes are alkaline with LILE (Ba and K)- and LREE-enrichment ((La/Yb) N > 4.3) and EM1-like Sr-Nd-Pb-Hf isotopic signature ((87Sr/86Sr) i > 0.706; ε Nd (t) 16.6, (207Pb/204Pb) i > 15.4, (208Pb/204Pb) i > 36.8, ε Hf (t) 3.7), and display similar EM1-like isotopic features ((87Sr/86Sr) i > 0.706; ε Nd (t) 16.7, (207Pb/204Pb) i > 15.4, (208Pb/204Pb) i > 36.9, ε Hf (t) 2.4) and EM1-like isotopic features((87Sr/86Sr) i > 0.706; ε Nd (t) 16.7, (207Pb/204Pb) i > 15.4, (208Pb/204Pb) i > 36.9, ε Hf (t) 3.7) and EM1-like Sr-Nd-Pb-Hf isotopic features ((87Sr/86Sr) i > 0.706; ε Nd(t) 16.7, (207Pb/204Pb) i > 15.4, (208Pb/204Pb) i > 36.9, ε Hf (t) 9.3) and EM1-like isotopic composition ((87Sr/86Sr) i > 0.705; ε Nd (t) 16.9, (207Pb/204Pb) i > 15.5, (208Pb/204Pb) i > 36.9, ε Hf (t) Hf isotopic signature ((87Sr/86Sr) i > 0.705; ε Nd (t) 16.9, (207Pb/204Pb) i > 15.5, (208Pb/204Pb) i > 36.9, ε Hf (t) < -8.6). Our data from the various mafic dyke suites suggest that the magmas were derived from EM1-like lithospheric mantle, corresponding to lithospheric mantle modified by the previously foundered lower crust beneath the eastern NCC. Our results suggest contrasting lithospheric evolution from Triassic (212 Ma) to Cretaceous (123 Ma) beneath the NCC. These mafic dykes mark an important phase of lithospheric thinning in the eastern North China Craton.

  1. Metal - Silicate Separation in a Deformation Regime: Implications for Early Differentiation Processes (United States)

    Rushmer, T.; Jones, J. H.; Gaetani, G.; Zanda, B.


    The segregation of metallic cores from silicate mantles is one of the earliest, and most important, differentiation process involved in the evolution of the Earth and other terrestrial planetary bodies. The physical segregation of Fe-rich metal from silicate imparted a strong geochemical signature on early silicate mantles due to the preferential incorporation of siderophile elements into the core. Reconciling our estimates of primary bulk silicate mantle with candidate planetary bulk compositions requires an understanding of the geochemical consequences of the different regimes in which core forming material may have been mobile. This includes not only the possible differentiation processes that occurred in the terrestrial planets, but also understanding the differentiation processes in the meteorite parent bodies. Although a magma ocean model is possible for efficient core formation, some scenarios call for segregation of the core from solid silicate and the geochemical consequences can be significantly different. Experimental studies are one way in which insight can be gained into the possible geochemical signatures of metal-silicate segregation. Deformation experiments in addition provide a dynamic component, which allows liquid metal to segregate from solid silicate. Starting materials are cored from a slab of the Kernouve fall which is composed of olivine, pyroxene, plagioclase, chromite and chlorapatite; Fe-Ni metal and sulfide form 20-25% of the sample. Experimental conditions are 1.0-1.4 GPa confining pressure with strain rates of 10-4/s to 10-6/s. Temperatures ranging from 900° C to 1050° C produce variable amounts of silicate melt and different mechanisms of metal segregation are observed. In experiments which are below the silicate solidus, mobility of FeS is extensive and deformation textures are cataclastic. Geochemical analyses shows that migration of Fe-S-Ni-O metal through fractures and along grain boundaries produces extensive modification to

  2. Lifetime Predictions of a Titanium Silicate Glass with Machined Flaws (United States)

    Tucker, Dennis S.; Nettles, Alan T.; Cagle, Holly


    A dynamic fatigue study was performed on a Titanium Silicate glass to assess its susceptibility to delayed failure and to compare the results with those of a previous study. Fracture mechanics techniques were used to analyze the results for the purpose of making lifetime predictions. The material strength and lifetime was seen to increase due to the removal of residual stress through grinding and polishing. Influence on time-to-failure is addressed for the case with and without residual stress present. Titanium silicate glass otherwise known as ultra-low expansion (ULE)* glass is a candidate for use in applications requiring low thermal expansion characteristics such as telescope mirrors. The Hubble Space Telescope s primary mirror was manufactured from ULE glass. ULE contains 7.5% titanium dioxide which in combination with silica results in a homogenous glass with a linear expansion coefficient near zero. delayed failure . This previous study was based on a 230/270 grit surface. The grinding and polishing process reduces the surface flaw size and subsurface damage, and relieves residual stress by removing the material with successively smaller grinding media. This results in an increase in strength of the optic during the grinding and polishing sequence. Thus, a second study was undertaken using samples with a surface finish typically achieved for mirror elements, to observe the effects of surface finishing on the time-to-failure predictions. An allowable stress can be calculated for this material based upon modulus of rupture data; however, this does not take into account the problem of delayed failure, most likely due to stress corrosion, which can significantly shorten lifetime. Fortunately, a theory based on fracture mechanics has been developed enabling lifetime predictions to be made for brittle materials susceptible to delayed failure. Knowledge of the factors governing the rate of subcritical flaw growth in a given environment enables the development of

  3. Crystallisation mechanism of a multicomponent lithium alumino-silicate glass

    Energy Technology Data Exchange (ETDEWEB)

    Wurth, R. [Otto-Schott-Institut, Jena University, Fraunhoferstr. 6, 07743 Jena (Germany); Pascual, M.J., E-mail: [Instituto de Ceramica y Vidrio, CSIC, Kelsen 5, 28049 Madrid (Spain); Mather, G.C.; Pablos-Martin, A.; Munoz, F.; Duran, A. [Instituto de Ceramica y Vidrio, CSIC, Kelsen 5, 28049 Madrid (Spain); Cuello, G.J. [Institut Laue-Langevin, Boite Postale 156, 38042 Grenoble Cedex 9 (France); Ruessel, C. [Otto-Schott-Institut, Jena University, Fraunhoferstr. 6, 07743 Jena (Germany)


    A base glass of composition 3.5 Li{sub 2}O Bullet-Operator 0.15 Na{sub 2}O Bullet-Operator 0.2 K{sub 2}O Bullet-Operator 1.15 MgO Bullet-Operator 0.8 BaO Bullet-Operator 1.5 ZnO Bullet-Operator 20 Al{sub 2}O{sub 3} Bullet-Operator 67.2 SiO{sub 2} Bullet-Operator 2.6 TiO{sub 2} Bullet-Operator 1.7 ZrO{sub 2} Bullet-Operator 1.2 As{sub 2}O{sub 3} (in wt.%), melted and provided by SCHOTT AG (Mainz), was used to study the crystallisation mechanism of lithium alumino-silicate glass employing X-ray diffraction combined with neutron diffraction and non-isothermal differential scanning calorimetry (DSC). A high-quartz solid solution of LiAlSi{sub 2}O{sub 6} with nanoscaled crystals forms at 750 Degree-Sign C. Quantitative Rietveld refinement of samples annealed at 750 Degree-Sign C for 8 h determined a crystallised fraction of around 59 wt.%. The room temperature crystallised phase adopts an ordered, {beta}-eucryptite-like structure (2 Multiplication-Sign 2 Multiplication-Sign 2 cell) with Li ordered in the structural channels. The Avrami parameter (n {approx} 4), calculated from DSC data using different theoretical approaches, indicates that bulk crystallisation occurs and that the number of nuclei increases during annealing. The activation energy of the crystallisation is 531 {+-} 20 kJ mol{sup -1}. - Highlights: Black-Right-Pointing-Pointer Nanoscaled high-quartz crystals from a multicomponent lithium alumino-silicate glass. Black-Right-Pointing-Pointer Combined X-ray and neutron diffraction structural refinement. Black-Right-Pointing-Pointer {beta}-Eucryptite-like structure (2 Multiplication-Sign 2 Multiplication-Sign 2 cell) with Li ordered in the structural channels. Black-Right-Pointing-Pointer 3-Dimensional bulk crystallisation mechanism with an increasing number of nuclei. Black-Right-Pointing-Pointer Usage and validation of an alternative approach to calculate the Avrami parameter.

  4. Triggers on sulfide saturation in Fe-Ti oxide-bearing, mafic-ultramafic layered intrusions in the Tarim large igneous province, NW China (United States)

    Cao, Jun; Wang, Christina Yan; Xu, Yi-Gang; Xing, Chang-Ming; Ren, Ming-Hao


    Three Fe-Ti oxide-bearing layered intrusions (Mazaertag, Wajilitag, and Piqiang) in the Tarim large igneous province (NW China) have been investigated for understanding the relationship of sulfide saturation, Platinum-group element (PGE) enrichment, and Fe-Ti oxide accumulation in layered intrusions. These mafic-ultramafic layered intrusions have low PGE concentrations (rocks are mainly attributed to PGE-depleted, parental magma that was produced by low degrees of partial melting of the mantle. The least contaminated rocks of the Mazaertag and Wajilitag intrusions have slightly enriched Os isotopic compositions with γOs(t = 280 Ma) values ranging from +13 to +23, indicating that the primitive magma may have been generated from a convecting mantle, without appreciable input of lithospheric mantle. The Mazaertag and Wajilitag intrusions have near-chondritic γOs(t) values (+13 to +60) against restricted ɛ Nd(t) values (-0.4 to +2.8), indicating insignificant crustal contamination. Rocks of the Piqiang intrusion have relatively low ɛ Nd(t) values of -3.1 to +1.0, consistent with ˜15 to 25 % assimilation of the upper crust. The rocks of the Mazaertag and Wajilitag intrusions have positive correlation of PGE and S, pointing to the control of PGE by sulfide. Poor correlation of PGE and S for the Piqiang intrusion is attributed to the involvement of multiple sulfide-stage liquids with different PGE compositions or sulfide-oxide reequilibration on cooling. These three layered intrusions have little potential of reef-type PGE mineralization. Four criteria are summarized in this study to help discriminate between PGE-mineralized and PGE-unmineralized mafic-ultramafic intrusions.

  5. Microstructure engineering of Portland cement pastes and mortars through addition of ultrafine layer silicates

    DEFF Research Database (Denmark)

    Lindgreen, Holger; Geiker, Mette; Krøyer, Hanne


    Pozzolanic submicron-sized silica fume and the non-pozzolanic micron- and nano-sized layer silicates (clay minerals) kaolinite, smectite and palygorskite have been used as additives in Portland cement pastes and mortars. These layer silicates have different particle shape (needles and plates...... is that the cement paste structure and porosity can be engineered by addition of selected layer silicates having specific particle shapes and surface properties (e.g., charge and specific surface area). This seems to be due to the growth of calcium-silicate hydrates (C-S-H) on the clay particle surfaces......), surface charge, and size (micron and nano). The structure of the resulting cement pastes and mortars has been investigated by atomic force microscopy (AFM), helium porosimetry, nitrogen adsorption (specific surface area and porosity), low-temperature calorimetry (LTC) and thermal analysis. The main result...

  6. Some observations on use of siliceous mineral waters in reduction of corrosion in RCC structures

    Digital Repository Service at National Institute of Oceanography (India)

    Venugopal, C.

    The corrosion-resisting characteristics of reinforcement in cement blended with siliceous mineral wastes viz. gold tailing and flyash have been evaluated by using an accelerated corrosion technique. The additions of these mineral admixtures...

  7. Geotechnical properties of two siliceous cores from the central Indian Ocean

    Digital Repository Service at National Institute of Oceanography (India)

    Khadge, N.H.

    Physical properties of the siliceous sediments from the Central Indian Basin are measured on two short cores. The properties such as water content, Atterberg limits, porosity specific gravity, wet density show the medium to high plastic sediment...

  8. Black silicate paints: Formulation and performance data on OSO-H (United States)

    Schutt, J. B.; Shai, C. M.


    Formulations and general procedures are given for making and applying space environmentally, as well as atmospherically stable black silicate paints. Compositions are given which meet spacecraft self-contamination requirements, have excellent heat resistance, and are strongly semiconductive.

  9. Polymer Derived Rare Earth Silicate Nanocomposite Protective Coatings for Nuclear Thermal Propulsion Systems Project (United States)

    National Aeronautics and Space Administration — The objective of this Phase I SBIR program is to develop polymer derived rare earth silicate nanocomposite environmental barrier coatings (EBC) for providing...

  10. Carbonation of metal silicates for long-term CO.sub.2 sequestration

    Energy Technology Data Exchange (ETDEWEB)

    Blencoe, James G.; Palmer, Donald A.; Anovitz, Lawrence M.; Beard, James S.


    In a preferred embodiment, the invention relates to a process of sequestering carbon dioxide. The process comprises the steps of: (a) reacting a metal silicate with a caustic alkali-metal hydroxide to produce a hydroxide of the metal formerly contained in the silicate; (b) reacting carbon dioxide with at least one of a caustic alkali-metal hydroxide and an alkali-metal silicate to produce at least one of an alkali-metal carbonate and an alkali-metal bicarbonate; and (c) reacting the metal hydroxide product of step (a) with at least one of the alkali-metal carbonate and the alkali-metal bicarbonate produced in step (b) to produce a carbonate of the metal formerly contained in the metal silicate of step (a).

  11. Polymer Derived Yttrium Silicate Ablative TPS Materials for Next-Generation Exploration Missions Project (United States)

    National Aeronautics and Space Administration — Through the proposed NASA SBIR program, NanoSonic will optimize its HybridSil® derived yttrium silicates to serve as next-generation reinforcement for carbon...


    National Research Council Canada - National Science Library

    V. U. Matsapulin; A. B. Toturbiev; V. I. Toturbiev; B. D. Toturbieva; V. I. Cherkashin


    The article analyzes the resource base, reserves and the use of siliceous rocks, their economic feasibility of the use for production of building materials of new generation with low-energy and other costs...

  13. Polymer Derived Rare Earth Silicate Nanocomposite Protective Coatings for Nuclear Thermal Propulsion Systems Project (United States)

    National Aeronautics and Space Administration — Leveraging a rapidly evolving state-of-the-art technical base empowered by Phase I NASA SBIR funding, NanoSonic's polymer derived rare earth silicate EBCs will...


    Directory of Open Access Journals (Sweden)



    Full Text Available Presented study of coal fluidized-bed ash solidification was accompanied with specific studies of alumino-silicates residues in ashes. The specific technology of fluid coal burning and its relatively low temperature combustion combines coal burning and decomposition of calcium carbonate added to the fluid layer in the main endeavor to capture all sulfur oxides. The burning temperature seems be decisive to the behavior of clayed residues and calcium carbonate decomposition in connection for the future solidification of fluidized bed ash. The calcareous substances in combination with alumino-silicate residues form solid bodies where silicates play decisive role of long-term stability and insolubility of obtained solids. The position of aluminum ions in clayed residues of burned coal were studied by MAS-NMR with attention on aluminum ion coordination to oxygen and formation of roentgen amorphous phase of poly-condensed calcium alumina-silicate.

  15. Effects of soil drenching of water-soluble potassium silicate on ...

    African Journals Online (AJOL)

    Effects of soil drenching of water-soluble potassium silicate on commercial avocado ( Persea americana Mill.) orchard trees infected with Phytophthora cinnamomi Rands on root density, canopy health, induction and concentration of phenolic com.

  16. Sulfide minerals as new Sm-Nd geochronometers for ore genesis dating of mafic-ultramafic layered intrusions (United States)

    Serov, Pavel; Ekimova, Nadezhda; Bayanova, Tamara


    neutron activation analysis (INAA) and ion probe. As shown, the level of REE in the sulfide phase determined by the ion probe is quite similar to that obtained by INAA. Although the concentrations of REE in the enstatite and the Fe, Si, Cr-rich inclusions are comparable to those in sulfide, estimates based on mass balance calculations show that the silicate inclusions would not noticeably contribute to the REE budget in sulfides (Kong et. al., 2000). These studies were supported by the RFBR 13-05-00493, OFI-M 13-05-12055, State Earth Division Program #4 and IGCP-599.

  17. [Colonization of silicate bacterium strain NBT in wheat roots]. (United States)

    Sheng, Xiafang


    The strain NBT of silicate bacterium was labelled with streptomycin, and a stable streptomycin resistance strain NBT was obtained. Its colonization dynamics and affecting factors in wheat rhizosphere were studied in agar plates and greenhouse pots were studied by counting the method with selective medium. The results of pot culture experiment showed that strain NBT could successfully colonize in the rhizosphere of wheat. In pot cultures of sterile soil, the highest colonization level (3.4 x 10(7) cfu.g-1 root soil) was reached on 9th day after seeds sown; at 54th day, the population of strain NBT tended to stable, and decreased to 1.4 x 10(4) cfu.g-1 root soil. In pot cultures of unsterile soil, the highest colonization level (3.8 x 10(7) cfu.g-1 root soil) was reached at 9th day, and the population of strain NBT tended to a stationary state at 60th day, with the numbers being 1.4 x 10(4) cfu.g-1 root soil. Some biological and abiotic factors could greatly influence the colonization of the beneficial microorganism.

  18. Optical analysis of samarium doped sodium bismuth silicate glass. (United States)

    Thomas, V; Sofin, R G S; Allen, M; Thomas, H; Biju, P R; Jose, G; Unnikrishnan, N V


    Samarium doped sodium bismuth silicate glass was synthesized using the melt quenching method. Detailed optical spectroscopic studies of the glassy material were carried out in the UV-Vis-NIR spectral range. Using the optical absorption spectra Judd-Ofelt (JO) parameters are derived. The calculated values of the JO parameters are utilized in evaluating the various radiative parameters such as electric dipole line strengths (Sed), radiative transition probabilities (Arad), radiative lifetimes (τrad), fluorescence branching ratios (β) and the integrated absorption cross- sections (σa) for stimulated emission from various excited states of Sm3+‡ ion. The principal fluorescence transitions are identified by recording the fluorescence spectrum. Our analysis revealed that the novel glassy system has the optimum values for the key parameters viz. spectroscopic quality factor, optical gain, stimulated emission cross section and quantum efficiency, which are required for a high performance optical amplifier. Calculated chromaticity co-ordinates (0.61, 0.38) also confirm its application potential in display devices. Copyright © 2016 Elsevier B.V. All rights reserved.

  19. A New Biphasic Dicalcium Silicate Bone Cement Implant

    Directory of Open Access Journals (Sweden)

    Fausto Zuleta


    Full Text Available This study aimed to investigate the processing parameters and biocompatibility of a novel biphasic dicalcium silicate (C2S cement. Biphasic α´L + β-C2Sss was synthesized by solid-state processing, and was used as a raw material to prepare the cement. In vitro bioactivity and biocompatibility studies were assessed by soaking the cement samples in simulated body fluid (SBF and human adipose stem cell cultures. Two critical-sized defects of 6 mm Ø were created in 15 NZ tibias. A porous cement made of the high temperature forms of C2S, with a low phosphorous substitution level, was produced. An apatite-like layer covered the cement’s surface after soaking in SBF. The cell attachment test showed that α´L + β-C2Sss supported cells sticking and spreading after 24 h of culture. The cement paste (55.86 ± 0.23 obtained higher bone-to-implant contact (BIC percentage values (better quality, closer contact in the histomorphometric analysis, and defect closure was significant compared to the control group (plastic. The residual material volume of the porous cement was 35.42 ± 2.08% of the initial value. The highest BIC and bone formation percentages were obtained on day 60. These results suggest that the cement paste is advantageous for initial bone regeneration.

  20. Mesoporous Calcium Silicate Nanoparticles with Drug Delivery and Odontogenesis Properties. (United States)

    Huang, Ching-Yuang; Huang, Tsui-Hsien; Kao, Chia-Tze; Wu, Yuan-Haw; Chen, Wan-Chen; Shie, Ming-You


    Calcium silicate (CS) -based materials play an important role in the development of endodontic materials that induce bone/cementum tissue regeneration and inhibit bacterial viability. The aim of this study was to prepare novel mesoporous CS (MesoCS) nanoparticles that have osteogenic, drug delivery, and antibacterial characteristics for endodontic materials and also have an excellent ability to develop apatite mineralization. The MesoCS nanoparticles were prepared using sol-gel methods. In addition, the mesoporous structure, specific surface area, pore volume, and morphology of the MesoCS nanoparticles were analyzed. The apatite mineralization ability, in vitro odontogenic differentiation, drug delivery, and antibacterial properties of the MesoCS nanoparticles were further investigated. The results indicate that the 200-nm-sized MesoCS nanoparticles synthesized using a facile template method exhibited a high specific surface area and pore volume with internal mesopores (average pore size = 3.05 nm). Furthermore, the MesoCS nanoparticles can be used as drug carriers to maintain sustained release of gentamicin and fibroblast growth factor-2 (FGF-2). The MesoCS-loaded FGF-2 might stimulate more odontogenic-related protein than CS because of the FGF-2 release. Based on this work, it can be inferred that MesoCS nanoparticles are potentially useful endodontic materials for biocompatible and osteogenic dental pulp tissue regenerative materials. Copyright © 2016 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  1. A New Biphasic Dicalcium Silicate Bone Cement Implant (United States)

    Murciano, Angel; Maté-Sánchez de Val, José E.


    This study aimed to investigate the processing parameters and biocompatibility of a novel biphasic dicalcium silicate (C2S) cement. Biphasic α´L + β-C2Sss was synthesized by solid-state processing, and was used as a raw material to prepare the cement. In vitro bioactivity and biocompatibility studies were assessed by soaking the cement samples in simulated body fluid (SBF) and human adipose stem cell cultures. Two critical-sized defects of 6 mm Ø were created in 15 NZ tibias. A porous cement made of the high temperature forms of C2S, with a low phosphorous substitution level, was produced. An apatite-like layer covered the cement’s surface after soaking in SBF. The cell attachment test showed that α´L + β-C2Sss supported cells sticking and spreading after 24 h of culture. The cement paste (55.86 ± 0.23) obtained higher bone-to-implant contact (BIC) percentage values (better quality, closer contact) in the histomorphometric analysis, and defect closure was significant compared to the control group (plastic). The residual material volume of the porous cement was 35.42 ± 2.08% of the initial value. The highest BIC and bone formation percentages were obtained on day 60. These results suggest that the cement paste is advantageous for initial bone regeneration. PMID:28773119

  2. Quaternary ammonium borohydride adsorption in mesoporous silicate MCM-48

    Energy Technology Data Exchange (ETDEWEB)

    Wolverton, Michael J [Los Alamos National Laboratory; Daemen, Luke L [Los Alamos National Laboratory; Hartl, Monika A [Los Alamos National Laboratory


    Inorganic borohydrides have a high gravimetric hydrogen density but release H2 only under energetically unfavorable conditions. Surface chemistry may help in lowering thermodynamic barriers, but inclusion of inorganic borohydrides in porous silica materials has proved hitherto difficult or impossible. We show that borohydrides with a large organic cation are readily adsorbed inside mesoporous silicates, particularly after surface treatment. Thermal analysis reveals that the decomposition thermodynamics of tetraalkylammonium borohydrides are substantially affected by inclusion in MCM-48. Inelastic neutron scattering (INS) data show that the compounds adsorb on the silica surface. Evidence of pore loading is supplemented by DSC/TGA, XRD, FTIR, and BET isotherm measurements. Mass spectrometry shows significant hydrogen release at lower temperature from adsorbed borohydrides in comparison with the bulk borohydrides. INS data measured for partially decomposed samples indicates that the decomposition of the cation and anion is likely simultaneous. Additionally, these data confirm the formation of Si-H bonds on the silica surface upon decomposition of adsorbed tetramethylammonium borohydride.

  3. Intraplate mantle oxidation by volatile-rich silicic magmas

    Energy Technology Data Exchange (ETDEWEB)

    Martin, Audrey M.; Médard, Etienne; Righter, Kevin; Lanzirotti, Antonio


    The upper subcontinental lithospheric mantle below the French Massif Central is more oxidized than the average continental lithosphere, although the origin of this anomaly remains unknown. Using iron oxidation analysis in clinopyroxene, oxybarometry, and melt inclusions in mantle xenoliths, we show that widespread infiltration of volatile (HCSO)-rich silicic melts played a major role in this oxidation. We propose the first comprehensive model of magmatism and mantle oxidation at an intraplate setting. Two oxidizing events occurred: (1) a 365–286 Ma old magmatic episode that produced alkaline vaugnerites, potassic lamprophyres, and K-rich calc-alkaline granitoids, related to the N–S Rhenohercynian subduction, and (2) < 30 Ma old magmatism related to W–E extension, producing carbonatites and hydrous potassic trachytes. These melts were capable of locally increasing the subcontinental lithospheric mantle fO2 to FMQ + 2.4. Both events originate from the melting of a metasomatized lithosphere containing carbonate + phlogopite ± amphibole. The persistence of this volatile-rich lithospheric source implies the potential for new episodes of volatile-rich magmatism. Similarities with worldwide magmatism also show that the importance of volatiles and the oxidation of the mantle in intraplate regions is underestimated.

  4. Nanoporous Calcium Silicate and PLGA Biocomposite for Bone Repair

    Directory of Open Access Journals (Sweden)

    Jiacan Su


    Full Text Available Nanoporous calcium silicate (n-CS with high surface area was synthesized using the mixed surfactants of EO20PO70EO20 (polyethylene oxide20(polypropylene oxide70(polyethylene oxide20, P123 and hexadecyltrimethyl ammonium bromide (CTAB as templates, and its composite with poly(lactic acid-co-glycolic acid (PLGA were fabricated. The results showed that the n-CS/PLGA composite (n-CPC with 20 wt% n-CS could induce a dense and continuous layer of apatite on its surface after soaking in simulated body fluid (SBF for 1 week, suggesting the excellent in vitro bioactivity. The n-CPC could promote cell attachment on its surfaces. In addition, the proliferation ratio of MG63 cells on n-CPC was significantly higher than PLGA; the results demonstrated that n-CPC had excellent cytocompatibility. We prepared n-CPC scaffolds that contained open and interconnected macropores ranging in size from 200 to 500 μm. The n-CPC scaffolds were implanted in femur bone defect of rabbits, and the in vivo biocompatibility and osteogenicity of the scaffolds were investigated. The results indicated that n-CPC scaffolds exhibited good biocompatibility, degradability, and osteogenesis in vivo. Collectively, these results suggested that the incorporation of n-CS in PLGA produced biocomposites with improved bioactivity and biocompatibility.

  5. Calcium silicate hydrates: Solid and liquid phase composition

    Energy Technology Data Exchange (ETDEWEB)

    Lothenbach, Barbara, E-mail: [Laboratory Concrete & Construction Chemistry, Empa (Switzerland); Nonat, André [ICB, UMR CNRS 6303 CNRS-Université de Bourgogne, Faculté des Sciences et Techniques, BP47870, 21078 Dijon Cedex (France)


    This paper presents a review on the relationship between the composition, the structure and the solution in which calcium silicate hydrate (C–S–H) is equilibrated. The silica chain length in C–S–H increases with the silicon concentration and the calcium content in the interlayer space with the calcium concentrations. Sodium and potassium are taken up in the interlayer space, preferentially at low calcium concentrations and thus by low Ca/Si C–S–H. Aluminium uptake in C–S–H increases strongly at higher aluminium concentrations in the solution. At low Ca/Si, aluminium substitutes silica in the bridging position, at Ca/Si > 1 aluminium is bound in TAH. Recently developed thermodynamic models are closely related to the structure of C–S–H and tobermorite, and able to model not only the solubility and the chemical composition of the C–S–H, but also to predict the mean silica chain length and the uptake of aluminium.

  6. Mechanical behavior of a composite interface: Calcium-silicate-hydrates

    Energy Technology Data Exchange (ETDEWEB)

    Palkovic, Steven D.; Moeini, Sina; Büyüköztürk, Oral, E-mail: [Department of Civil and Environmental Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States); Yip, Sidney [Department of Nuclear Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States)


    The generalized stacking fault (GSF) is a conceptual procedure historically used to assess shear behavior of defect-free crystalline structures through molecular dynamics or density functional theory simulations. We apply the GSF technique to the spatially and chemically complex quasi-layered structure of calcium-silicate-hydrates (C-S-H), the fundamental nanoscale binder within cementitious materials. A failure plane is enforced to calculate the shear traction-displacement response along a composite interface containing highly confined water molecules, hydroxyl groups, and calcium ions. GSF simulations are compared with affine (homogeneous) shear simulations, which allow strain to localize naturally in response to the local atomic environment. Comparison of strength and deformation behavior for the two loading methods shows the composite interface controls bulk shear deformation. Both models indicate the maximum shear strength of C-S-H exhibits a normal-stress dependency typical of cohesive-frictional materials. These findings suggest the applicability of GSF techniques to inhomogeneous structures and bonding environments, including other layered systems such as biological materials containing organic and inorganic interfaces.

  7. Efficacy of dispersion of magnesium silicate (talc in papermaking

    Directory of Open Access Journals (Sweden)

    Vipul Singh Chauhan


    Full Text Available The understanding of the dispersion chemistry of papermaking grade fillers is as important as their effect on paper. Magnesium silicate (talc is one of the major fillers used for papermaking. It is hydrophobic and chemically inert. The dispersion chemistry of talc of different particle sizes was studied with wetting agent (non-ionic triblock copolymer and anionic dispersant (sodium salt of polyacrylic acid. Both wetting agent and dispersant were added in talc slurry separately and in combination. The dispersion behavior was studied through measuring the Brookfield viscosity. The wetted and dispersed talc was also added to paper to understand its effect on papermaking process and paper properties. Wetting and dispersion changed the colloidal charge chemistry of talc making it more anionic which reduced the talc retention in paper. Lowering the particle size of talc significantly improved the light scattering coefficient (LSC of paper and decreased its retention. Controlling colloidal charge of papermaking suspension with cationic polyacrylamide polymer helped in protecting the retention of talc without affecting the LSC of both filler and paper.

  8. Silicate grout curtains behaviour for the protection of coastal aquifers

    Energy Technology Data Exchange (ETDEWEB)

    Elektorowicz, M.; Chifrina, R.; Hesnawi, R. [Concordia Univ., Montreal, Quebec (Canada)


    Tests were performed to evaluate the behaviour of silicate grout with different reagents (ethylacetate - formamide SA and calcium chloride SC) in pure silica sand and natural soils from coastal areas containing organic matter, clayey soil and silica sand. The grouted specimens were tested with simulated fresh and salt water. The setting process during chemical grouting in the soil and sand was studied. The grouting of soil and sand with SA caused a transfer to the environment of some compounds: sodium formate, sodium acetate, ammonia and part of the initial ethylacetate and formamide. This process had a tendency to decrease for approximately 4 months. The stability of specimens was low. The grouting of soil and sand with SC caused no significant contamination of the environment. The increase of pH of environmental water was even less than with SA grouting. Also, the stability of specimens is higher in comparison with SA grouting. Salt water protected the specimens grouted with SA and SC from destruction and prevented contamination.

  9. Understanding controlled drug release from mesoporous silicates: theory and experiment. (United States)

    Ukmar, T; Maver, U; Planinšek, O; Kaučič, V; Gaberšček, M; Godec, A


    Based on the results of carefully designed experiments upgraded with appropriate theoretical modeling, we present clear evidence that the release curves from mesoporous materials are significantly affected by drug-matrix interactions. In experimental curves, these interactions are manifested as a non-convergence at long times and an inverse dependence of release kinetics on pore size. Neither of these phenomena is expected in non-interacting systems. Although both phenomena have, rather sporadically, been observed in previous research, they have not been explained in terms of a general and consistent theoretical model. The concept is demonstrated on a model drug indomethacin embedded into SBA-15 and MCM-41 porous silicates. The experimental release curves agree exceptionally well with theoretical predictions in the case of significant drug-wall attractions. The latter are described using a 2D Fokker-Planck equation. One could say that the interactions affect the relative cross-section of pores where the local flux has a non-vanishing axial component and in turn control the effective transfer of drug into bulk solution. Finally, we identify the critical parameters determining the pore size dependence of release kinetics and construct a dynamic phase diagram of the various resulting transport regimes. Copyright © 2011 Elsevier B.V. All rights reserved.

  10. Distribution of rubidium between sodic sanidine and natural silicic liquid (United States)

    Noble, D.C.; Hedge, C.E.


    Phenocrysts of sodic sanidine from twelve upper Cenozoic units of silicic ash-flow tuff and lava from the Western United States contain from 0.25 to 0.45 the Rb present in the associated groundmass materials. The ratios of potassium to rubidium in the sanidines are, on the average, about four times greater than those of the groundmass. Separation of phenocrystic sanidine from salic melts provides an efficient method for raising the Rb content and lowering the K/Rb ratio of the melts, although the amount of differentiation probably is limited by continuous reequilibration of the alkalis between crystal and liquid phases through ion exchange. Syenites of cumulate origin will have appreciably lower Rb contents and higher K/Rb ratios than the melts from which they precipitated. Available data on the distribution of Rb between synthetic biotite and K-sanidine demonstrate that the separation of biotite probably will not deplete salic melts in Rb relative to K. ?? 1970 Springer-Verlag.

  11. Pt, Au, Pd and Ru Partitioning Between Mineral and Silicate Melts: The Role of Metal Nanonuggets (United States)

    Malavergne, V.; Charon, E.; Jones, J.; Agranier, A.; Campbell, A.


    The partition coefficients of Pt and other Pt Group Elements (PGE) between metal and silicate D(sub Metal-Silicate) and also between silicate minerals and silicate melts D(sub Metal-Silicate) are among the most challenging coefficients to obtain precisely. The PGE are highly siderophile elements (HSE) with D(sub Metal-Silicate) >10(exp 3) due to the fact that their concentrations in silicates are very low (ppb to ppt range). Therefore, the analytical difficulty is increased by the possible presence of HSE-rich-nuggets in reduced silicate melts during experiments). These tiny HSE nuggets complicate the interpretation of measured HSE concentrations. If the HSE micro-nuggets are just sample artifacts, then their contributions should be removed before calculations of the final concentration. On the other hand, if they are produced during the quench, then they should be included in the analysis. We still don't understand the mechanism of nugget formation well. Are they formed during the quench by precipitation from precursor species dissolved homogeneously in the melts, or are they precipitated in situ at high temperature due to oversaturation? As these elements are important tracers of early planetary processes such as core formation, it is important to take up this analytical and experimental challenge. In the case of the Earth for example, chondritic relative abundances of the HSE in some mantle xenoliths have led to the concept of the "late veneer" as a source of volatiles (such as water) and siderophiles in the silicate Earth. Silicate crystal/liquid fractionation is responsible for most, if not all, the HSE variation in the martian meteorite suites (SNC) and Pt is the element least affected by these fractionations. Therefore, in terms of reconstructing mantle HSE abundances for Mars, Pt becomes a very important player. In the present study, we have performed high temperature experiments under various redox conditions in order to determine the abundances of Pt, Au

  12. Metal-silicate partitioning experiments in the diamond anvil cell: A comment on potential analytical errors (United States)

    Wade, Jon; Wood, Bernard J.


    We have performed simulations of the electron microbeam analysis of metal-silicate partitioning experiments in which a small (˜50 μm) ball of metal is embedded in a silicate matrix. This geometry approximates that found in many high pressure diamond-cell experiments aimed at determining the partition coefficients (Di) of elements between metal and silicate. The simulations involved using the (publicly available) Monte Carlo simulation package PENEPMA which is based on the general-purpose electron-photon transport code PENELOPE. The code allows complex geometrical structures to be defined by quadric surfaces, which enclose homogeneous materials specified by the user. The package simulates both electron and photon transport, keeps track of the X-ray production mechanism and includes the continuum contribution. Our principal results came from simulating the effects of secondary fluorescence on the apparent metal-silicate partition coefficient of Ni for the case of an Ni-rich metal (26.8% Ni, 73.2% Fe) embedded in a silicate matrix. If, as is frequently the case, analysis of the silicate is performed 5-10 μm from the silicate-metal interface then secondary fluorescence of Ni in the metal will increase the apparent NiO concentration in the silicate by ˜1000 ppm. In the case considered, this is 25% of the Ni content of the silicate and the fluorescence effect decreases the apparent DNi from 110 to 84. For this type of experiment, therefore, the fluorescence effect reduces the apparent partition coefficient. We performed similar simulations of the analysis of the centre of a 10 μm diameter metal ball embedded in the silicate matrix to determine apparent Si and O concentrations in the metal. In this case, because the electrons do not penetrate so far into the metal, the fluorescence effect is very small and can be neglected. Finally, we show that focused ion beam (FIB) sections, while providing the potential physically to separate metal from silicate present

  13. Emission and extinction of ground and vapor-condensed silicates from 4 to 14 microns and the 10 micron silicate feature (United States)

    Stephens, J. R.; Rusell, R. W.


    Emission and absorption spectra from 4 to 14 microns of ground and laser-vaporized olivine and enstatite silicates are compared with the 10-micron emission feature of the Orion Trapezium. The agreement in band center and shape between the amorphous laser-vaporized olivine sample and the Trapezium feature suggests that amorphous silicate grains of approximately olivine composition may be a major constituent of interstellar dust. Differences between the emission and absorption spectral profiles (absorption plus scattering) show characteristics that could be used as a sensitive probe of the morphology of interstellar grain systems when high signal-to-noise ratio (30-100) observational spectra become available.

  14. Experimental calibration of a new oxybarometer for silicic magmas based on vanadium partitioning between magnetite and silicate melt (United States)

    Arató, Róbert; Audétat, Andreas


    Partition coefficients of vanadium between magnetite and rhyolitic silicate melt, DVmgt/melt, were experimentally determined as a function of oxygen fugacity (0.7-4.0 log units above the fayalite-magnetite-quartz buffer), temperature (800-1000 °C), melt alumina saturation index (ASI = 0.74-1.14), magnetite composition (0.2-14 wt% TiO2) and pressure (1-5 kbar; at H2O saturation). Experiments were performed by equilibrating small (≤20 μm), V-free magnetite grains in V-doped silicate melts (∼100 ppm V) and then analyzing both phases by LA-ICP-MS. Attainment of equilibrium was demonstrated by several reversal experiments. The results suggest that DVmgt/melt depends strongly on fO2, increasing by 1.5-1.7 log units from the MnO-Mn3O4 buffer to the Ni-NiO buffer, and to lesser (but still considerable) extents on melt alumina saturation index (ASI; increasing by 0.3-0.7 log units over 0.4 ASI units) and temperature (increasing by 0.3-0.7 log units over a 200 °C interval at a fixed fO2 buffer). Magnetite composition and melt water content seem to have negligible effects. The data were fitted by the following linear regression equation: in which temperature is given in K, ASI refers to molar Al2O3/(CaO + Na2O + K2O) and ΔFMQ refers to the deviation of fO2 (in log units) from the fayalite-magnetite-quartz buffer. This equation reproduces all of our data within 0.3 log units, and 89% of them within 0.15 log units. The main advantages of this new oxybarometer over classical magnetite-ilmenite oxybarometry are (1) that it can be applied to rocks that do not contain ilmenite, and (2) that it is easier to apply to slowly-cooled rocks such as granites.

  15. Adsorption of Free Fatty Acid from Crude Palm Oil on Magnesium Silicate Derived from Rice Husk

    Directory of Open Access Journals (Sweden)

    Pornsawan Assawasaengrat


    Full Text Available Magnesium silicate with various silica and magnesium oxide ratios (SiO2/MgO ratios was used as the adsorbent for a study of adsorption of free fatty acid (FFA in crude palm oil (CPO. Magnesium silicate was prepared from magnesium nitrate or magnesium sulfate solution precipitated with a solution of sodium silicate derived from rice husk. SiO2/MgO ratios of the magnesium silicate synthesized from magnesium nitrate and magnesium sulfate were 3.93, 3.75, 2.74, 2.40, 1.99 and 3.96, 3.61, 3.51, 2.91, 2.69, respectively. FFA adsorption on the magnesium silicate was carried out by adding 1 gram of the adsorbent to 50 grams of CPO and shaking for 1 hour at 50oC. It was found that SiO2/MgO ratio of 1.99 had the highest adsorption capacities of 185 mg of FFA per gram of adsorbent. In addition, increasing of SiO2/MgO ratios of magnesium silicate was found to reduce the adsorption capacities due to decreasing of FFA chemisorption. The effect of dosage amount to equilibrium adsorption capacities were carried out by adding different amount of magnesium silicate (SiO2/MgO ratio of 1.99 to 50 grams of CPO. The result showed that efficiency decreased when dosage increased. The Fruendlich and Langmuir isotherm were applied to describe this absorption system. The values of maximum sorption capacity (Q0 and Langmuir's sorption affinity (b in the Langmuir equation obtained by linear-regression were minus values which were physically meanigless. Thus, FFA adsorption on magnesium silicate was both physisorption and chemisorption and well represented by the Fruenlich isotherm.

  16. Synthesis and optical features of an europium organic-inorganic silicate hybrid

    Energy Technology Data Exchange (ETDEWEB)

    Franville, A.C.; Zambon, D.; Mahiou, R.; Chou, S.; Cousseins, J.C. [Universite Blaise Pascal, Aubiere (France). Lab. des Materiaux Inorganiques; Troin, Y. [Laboratoire de Chimie des Heterocycles et des Glucides, EA 987, Universite Blaise-Pascal and ENSCCF, F-63177 Aubiere Cedex (France)


    A europium organic-inorganic silicate hybrid was synthesized by grafting a coordinative group (dipicolinic acid) to a silicate network precursor (3-aminopropyltriethoxysilane) via a covalent bonding. Sol-gel process and complexation were performed using different experimental conditions. The hybrid materials, in particular the Eu{sup 3+} coordination mode, were characterized by infrared and luminescence spectroscopies. Morphology of the materials and TG analysis showed that grafted silica enhanced thermal and mechanical resistances of the organic part. (orig.) 7 refs.

  17. Assessment of Fe(III) and Eu(III) complexation by silicate in aqueous solutions (United States)

    Patten, James T.; Byrne, Robert H.


    Prior investigations of Eu3+ complexation by silicate have led to predictions that rare earth silicate complexes (REESiO(OH)32+) are the dominant species of REEs in deep waters of the Atlantic and Pacific Oceans. The proposed importance of REE-silicate complexes has been used as a foundation to explain oceanic REE profiles. In the present work, we examine the significance of rare earth element complexation by silicate ions. As one fundamental means of assessing prior depictions of REE-silicate formation constant behavior, our work examines the comparative stability constant behavior of Eu(III) and Fe(III). Plots of Eu(III) complexation constants against Fe(III) formation constants, in conjunction with experimental determinations of FeSiO(OH)32+ formation constants, indicate that previously published EuSiO(OH)32+ formation constants are substantially overestimated. Assessment of prior EuSiO(OH)32+ formation constant determinations reveals that results obtained in the presence and absence of silicic acid polymerization are inconsistent. Much larger EuSiO(OH)32+ formation constants are obtained in the presence of polymeric silica. Reanalysis of complexation results obtained under conditions of minimal silicate polymerization leads to a EuSiO(OH)32+ formation constant that is smaller than previously published estimates by as much as a factor of ∼25. The dramatically reduced magnitude of Siβ1(Eu) relative to previously published results indicates that the role of silicate complexation in oceanic REE cycling is much less significant than previously proposed. The spectrophotometric investigations of FeSiO(OH)32+ formation in the present study yield the first characterization of FeSiO(OH)32+ formation constant behavior as a function of ionic strength:

  18. (Isotope tracer studies of diffusion in silicates and of geological transport processes using actinide elements)

    Energy Technology Data Exchange (ETDEWEB)

    Wasserburg, G.J.


    This report consists of sections entitled resonance ionization mass spectrometry of Os, Mg self-diffusion in spinel and silicate melts, neotectonics: U-Th ages of solitary corals from the California coast, uranium-series evidence on diagenesis and hydrology of carbonates of Barbados, diffusion of H{sub 2}O molecules in silicate glasses, and development of an extremely high abundance sensitivity mass spectrometer.


    Energy Technology Data Exchange (ETDEWEB)

    Suh, Kyung-Won, E-mail: [Department of Astronomy and Space Science, Chungbuk National University, Cheongju-City, 28644 (Korea, Republic of)


    IRAS 09425-6040 (I09425) is a silicate carbon star with conspicuous crystalline silicate and water-ice features and emission excesses in the far-infrared and millimeter (mm) wavelength ranges. To understand properties of the dust envelope of I09425, we propose a physical model based on the observations and known properties of asymptotic giant branch stars and dust. We perform radiative transfer model calculations using multiple dust shells and disks with various dust species. We compare the model results with the observed spectral energy distribution (SED) acquired with different telescopes. We find that the physical model for I09425 using multiple shells of carbon and silicate dust and multiple disks of amorphous and crystalline silicates reproduces the observed SED fairly well. This object looks to have detached cold O-rich (silicate and water-ice) dust shells, which could be remnants of the recent chemical transition from O to C and an inner C-rich dust shell. A long-lived thin disk of very large silicate grains can reproduce the emission excess in the mm wavelength band and a recently formed thick disk of crystalline silicates can reproduce the prominent emission features in the spectral range 8–45 μm. The highly crystallized silicates could be recently formed by high temperature annealing due to the last O-rich superwind just before the chemical transition of the central star. I09425 could be a rare object that has the remnants of past O-rich stellar winds in the outer shells as well as in the circumbinary disks.

  20. Fungicides and silicate clay on the control of antracnosis in yellow passionfruit


    Medeiros, André Martins; Autônomo; Peruch, Luiz Augusto Martins; Estação Experimental de Urussanga


    The anthracnose, caused by Glomerella cingulata (anamorf Colletotrichum gloeosporioides), is the most important fungal disease for aerial parts of yellow passionfruit. However, few studies about anthracnose control in field conditions have been published. The objective of this research was to evaluate silicate clay and fungicides for anthracnose control. Treatments evaluated were: tebuconazole (20g i.a./100L), copper oxychloride (180g i.a./100L), silicate clay (15g /L) and control (untreated ...

  1. Molecular Dynamics Modeling of Hydrated Calcium-Silicate-Hydrate (CSH) Cement Molecular Structure (United States)


    paste consisting of starting configuration of dry cement powder and water mixture by itself is a complex, multi-scale material system. Though...high pressure molecular structural behavior of the hydrated CSH. Portland cement in the powder form consists of four different major constituents...Tricalcium silicate (C3S), Di-Calcium silicate (C2S), Tri-Calcium aluminate (C3A), and Tetra calcium aluminoferrite (C4AF) [1]. Different mixture

  2. AC electrical breakdown phenomena of epoxy/layered silicate nanocomposite in needle-plate electrodes. (United States)

    Park, Jae-Jun; Lee, Jae-Young


    Epoxy/layered silicate nanocomposite for the insulation of heavy electric equipments were prepared by dispersing 1 wt% of a layered silicate into an epoxy matrix with a homogenizing mixer and then AC electrical treeing and breakdown tests were carried out. Wide-angle X-ray diffraction (WAXD) analysis and transmission electron microscopy (TEM) observation showed that nano-sized monolayers were exfoliated from a multilayered silicate in the epoxy matrix. When the nano-sized silicate layers were incorporated into the epoxy matrix, the breakdown rate in needle-plate electrode geometry was 10.6 times lowered than that of the neat epoxy resin under the applied electrical field of 520.9 kV/mm at 30 degrees C, and electrical tree propagated with much more branches in the epoxy/layered silicate nanocomposite. These results showed that well-dispersed nano-sized silicate layers retarded the electrical tree growth rate. The effects of applied voltage and ambient temperature on the tree initiation, growth, and breakdown rate were also studied, and it was found that the breakdown rate was largely increased, as the applied voltage and ambient temperature increased.

  3. Silicate Earth’s missing niobium may have been sequestered into asteroidal cores (United States)

    Münker, Carsten; Fonseca, Raúl O. C.; Schulz, Toni


    Geochemical models describing the behaviour of niobium during Earth’s growth rely on the general paradigm that niobium was delivered by Earth’s asteroidal building blocks at chondritic abundances. This paradigm is based on the observation that niobium is traditionally regarded as a refractory and strongly lithophile element, and thus stored in the silicate portions of Earth and differentiated asteroids. However, Earth’s silicate mantle is instead selectively depleted in niobium, in marked contrast to the silicate mantles of many asteroids and smaller planets that apparently lack any significant depletion in niobium. Here we present results of high-precision measurements for niobium and other lithophile elements in representative meteorites from various small differentiated asteroids. Our data, along with the results of low-pressure experiments, show that in more reduced asteroids--such as Earth’s first building blocks--niobium is moderately chalcophile and more so than its geochemical twin tantalum by an order of magnitude. Accordingly, niobium can be sequestered into the cores of more reduced asteroids during differentiation via the segregation of sulfide melts in a carbon-saturated environment. We suggest that the niobium deficit in Earth’s silicate mantle may be explained by the Earth’s silicate mantle preferentially accreting the silicate portions of reduced asteroidal building blocks.

  4. The Preparation of Flaky Layered Carbon by Using Layered Silicate Template

    Energy Technology Data Exchange (ETDEWEB)

    Kwon, Oh Yun [Yosu National University, Yeosu (Korea, Republic of); Park, Kyeong Won [Gyeongsang National University, Jinju (Korea, Republic of)


    Porous layered carbons with well-developed flake structure were successfully prepared by using layered silicate template. The gallery of layered silicate is composed of two-dimensional spaces with nano scale, which can have a role as nano reactor for chemicals introduced into the gallery. It confirmed that PFO, in this nano reactor, could be transformed easily to layered carbon or graphite structure by the heat treatment, allowing layered carbon-layered silicate nanocomposite (LC-LSN) piled carbon film or graphite sheet in layers of layered silicate. The removal of template from LC-LSN resulted in separated and well-developed flaky layered carbon or graphite with large surface area of 160-240 m{sup 2}/g, which was quite different from carbon black and activated carbon. In recent years, the preparation and application of nanostructure carbon materials such as carbon nanotube and nanoporous carbon has attracted increasing interests. We now report on the preparation of flaky layered carbon by using layered silicates as template. These layered carbons should be applicable potentially in technical field such as the electronics, catalytic and hydrogen-storage system. Layered silicates have exchangeable cations such as Na{sup +}, K{sup +}, Ca{sup 2+} and Mg{sup 2+} in the interlayer space.

  5. Trends in the adsorption and reactivity of hydrogen on magnesium silicate nanoclusters. (United States)

    Oueslati, Ichraf; Kerkeni, Boutheïna; Bromley, Stefan T


    We study nanoclusters of Mg-rich olivine and pyroxene (having (MgO)6(SiO2)3 and (MgO)4(SiO2)4 compositions) with respect to their reactivity towards hydrogen atoms, using density functional calculations. Ultrasmall silicate particles are fundamental intermediates in cosmic dust grain formation and processing, and are thought to make up a significant mass fraction of the grain population. Due to their nanoscale dimensions and high surface area to bulk ratios, they are likely to also have a disproportionately large influence on surface chemistry in the interstellar medium. This work investigates the potential role of silicate nanoclusters in vital interstellar hydrogen-based chemistry by studying atomic H adsorption and H2 formation. Our extensive set of calculations confirm the generality of a Brønsted-Evans-Polanyi (BEP) relation between the H2 reaction barrier and the 2Hchem binding energy, suggesting it to be independent of silicate dust grain shape, size, crystallinity and composition. Our results also suggest that amorphous/porous grains with forsteritic composition would tend to dissociate H2, but relatively Mg-poor silicate grains (e.g. enstatite composition) and/or more crystalline/compact silicate grains would tend to catalyse H2 formation. The high structural thermostability of silicate nanoclusters with respect to the heat released during exothermic H2 formation reactions is also verified.

  6. [Effects of silicate on the community structure of phytoplankton in enclosures]. (United States)

    Sun, Ling; Jin, Xiang-can; Yang, Wei; Xu, Min; Zhong, Yuan; Zhu, Lin; Zhuang, Yuan-yi


    Controlling the concentrations of silicate, enclosure experiments were conducted in Xinkai Lake to investigate the influence of Si concentration on the growth and succession of phytoplankton communities in a eutrophic freshwater. The results show that with the addition of silicate, the biomass of diatoms increased and the ratio of diatom species to the total significantly increased from 10.2% to 22.1% . While the species percent of Cyanobacteria and Chlorophyta decreased to 61.5%, as compared with 76.8% in control. Several diatom species, such as Synedra ulna, Nitzschia denticula, Nitzschia acicularis, Gomphonema constrictum var. capitata, Gomphonema olivaceum, which were not found in control, were observed in the silicate-enriched treatments. The Shannon indices of 2.17 +/- 0.40 and 2.12 +/- 0.21 were obtained from the medium-Si (atomic ratio N:Si:P = 16:8:1) and high-Si ( N:Si:P = 16:16:1) treatments, which were higher than that of the control enclosure (1.89 +/- 0.55, without silicate addition). At the late phase of the experiments, algal blooms mainly composed of Microcystis aeruginosa appeared in control but not in the silicate-enriched enclosures. The enrichment of silicate can promote the growth of diatoms and the other algal species and change the dominance of few Cyanobacteria and Chlorophyte species. Therefore, it can elevate the algal biodiversity of an aquatic ecosystem and weaken the cyanobacterial blooms to a certain degree.

  7. SON68 glass dissolution driven by magnesium silicate precipitation (United States)

    Fleury, Benjamin; Godon, Nicole; Ayral, André; Gin, Stéphane


    Experimental results are reported on the effect of magnesium silicate precipitation on the mechanisms and rate of borosilicate glass dissolution. Leaching experiments with SON68 glass, a borosilicate containing no Mg, were carried out in initially deionized water at 50 °C with a glass-surface-area-to-solution-volume ratio of 20,000 m-1. After 29 days of alteration the experimental conditions were modified by the addition of Mg to trigger the precipitation of Mg-silicate. Additional experiments were conducted to investigate the importance of other parameters such as pH or dissolved silica on the mechanisms of precipitation of Mg-silicates and their consequences on the glass dissolution rate. Mg-silicates precipitate immediately after Mg is added. The amount of altered glass increases with the quantity of added Mg, and is smaller when silicon is added in solution. A time lag is observed between the addition of magnesium and the resumption of glass alteration because silicon is first provided by partial dissolution of the previously formed alteration gel. It is shown that nucleation does not limit Mg-silicate precipitation. A pH above 8 is necessary for the phase to precipitate under the investigated experimental conditions. On the other hand the glass alteration kinetics limits the precipitation if the magnesium is supplied in solution at a non-limiting rate. The concentration of i in solution was analyzed as well as that of boron. The quantity of i released from the glass is estimated with the assumption that i and B are released congruently at the glass dissolution front. The remained quantity of the element i is then supposed to be in the gel or in the secondary phase. In this paper, we do not make a difference between gel and hydrated glass using the same word 'gel' whereas Gin et al. [40] makes this difference. Recent papers [40,41] discussed about different key issues related to the passivation properties of the alteration layer including the hydrated glass

  8. Water-bearing, high-pressure Ca-silicates (United States)

    Németh, Péter; Leinenweber, Kurt; Ohfuji, Hiroaki; Groy, Thomas; Domanik, Kenneth J.; Kovács, István J.; Kovács, Judit S.; Buseck, Peter R.


    Water-bearing minerals provide fundamental knowledge regarding the water budget of the mantle and are geophysically significant through their influence on the rheological and seismic properties of Earth's interior. Here we investigate the CaO-SiO2-H2O system at 17 GPa and 1773 K, corresponding to mantle transition-zone condition, report new high-pressure (HP) water-bearing Ca-silicates and reveal the structural complexity of these phases. We document the HP polymorph of hartrurite (Ca3SiO5), post-hartrurite, which is tetragonal with space group P4/ncc, a = 6.820 (5), c = 10.243 (8) Å, V = 476.4 (8) Å3, and Z = 4, and is isostructural with Sr3SiO5. Post-hartrurite occurs in hydrous and anhydrous forms and coexists with larnite (Ca2SiO4), which we find also has a hydrous counterpart. Si is 4-coordinated in both post-hartrurite and larnite. In their hydrous forms, H substitutes for Si (4H for each Si; hydrogrossular substitution). Fourier transform infrared (FTIR) spectroscopy shows broad hydroxyl absorption bands at ∼3550 cm-1 and at 3500-3550 cm-1 for hydrous post-hartrurite and hydrous larnite, respectively. Hydrous post-hartrurite has a defect composition of Ca2.663Si0.826O5H1.370 (5.84 weight % H2O) according to electron-probe microanalysis (EPMA), and the Si deficiency relative to Ca is also observed in the single-crystal data. Hydrous larnite has average composition of Ca1.924Si0.851O4H0.748 (4.06 weight % H2O) according to EPMA, and it is in agreement with the Si occupancy obtained using X-ray data collected on a single crystal. Superlattice reflections occur in electron-diffraction patterns of the hydrous larnite and could indicate crystallographic ordering of the hydroxyl groups and their associated cation defects. Although textural and EPMA-based compositional evidence suggests that hydrous perovskite may occur in high-Ca-containing (or low silica-activity) systems, the FTIR measurement does not show a well-defined hydroxyl absorption band for this

  9. Combined effect of carbonate and biotite dissolution in landslides biases silicate weathering proxies (United States)

    Emberson, R.; Galy, A.; Hovius, N.


    Long-term estimates of the dissolution of silicate rock are generally derived from a range of isotopic proxies, such as the radiogenic strontium isotope ratio (87Sr/86Sr), which are preserved in sediment archives. For these systems to fairly represent silicate weathering, the changes in isotopic ratios in terrestrial surface waters should correspond to changes in the overall silicate dissolution. This assumes that the silicate mineral phases that act as sources of a given isotope dissolve at a rate that is proportional to the overall silicate weathering. Bedrock landsliding exhumes large quantities of fresh rock for weathering in transient storage, and rapid weathering in these deposits is controlled primarily by dissolution of the most reactive phases. In this study, we test the hypothesis that preferential weathering of these labile minerals can decouple the dissolution of strontium sources from the actual silicate weathering rates in the rapidly eroding Western Southern Alps (WSA) of New Zealand. We find that rapid dissolution of relatively radiogenic calcite and biotite in landslides leads to high local fluxes in strontium with isotopic ratios that offer no clear discrimination between sources. These higher fluxes of radiogenic strontium are in contrast to silicate weathering rates in landslides that are not systematically elevated. On a mountain belt scale, radiogenic strontium fluxes are not coupled to volumes of recent landslides in large (>100 km2) catchments, but silicate weathering fluxes are. Such decoupling is likely due first to the broad variability in the strontium content of carbonate minerals, and second to the combination of radiogenic strontium released from both biotite and carbonate in recent landslides. This study supports previous work suggesting the limited utility of strontium isotopes as a system to study silicate weathering in the WSA. Crucially however, in settings where bedrock landsliding is a dominant erosive process there is

  10. Sodium silicate solutions from dissolution of glasswastes. Statistical analysis

    Directory of Open Access Journals (Sweden)

    Torres-Carrasco, M.


    Full Text Available It has studied the solubility process of four different waste glasses (with different particle sizes, 125 µm in alkaline solutions (NaOH and NaOH/Na₂CO₃ and water as a reference and under different conditions of solubility (at room temperature, at 80°C and a mechano-chemical process. Have established the optimal conditions of solubility and generation of sodium silicates solutions, and these were: the smaller particle size (Se ha estudiado el proceso de solubilidad de cuatro diferentes residuos vítreos (con distintas granulometrías, 125 µm en disoluciones alcalinas de NaOH y NaOH/Na₂CO₃ y agua como medio de referencia y bajo distintas condiciones de solubilidad (a temperatura ambiente, a 80°C y con un proceso mecano-químico. Se han establecido las condiciones óptimas de solubilidad y generación de disoluciones de silicato sódico, y estas son: menor tamaño de partícula del residuo vítreo (inferior a 45 µm, con la disolución de NaOH/Na₂CO₃ y tratamiento térmico a 80°C durante 6 horas de agitación. El análisis estadístico realizado a los resultados obtenidos da importancia a las variables estudiadas y a las interacciones de las mismas. A través de ²⁹Si RMN MAS se ha confirmado la formación, tras los procesos de disolución, de un silicato monomérico, apto para su utilización como activador en la preparación de cementos y hormigones alcalinos.

  11. Fluorinated silicate glass for conventional and holographic optical elements (United States)

    Glebov, Leonid


    This presentation is a survey of results of a long-term research at the laboratory of photoinduced processes at CREOL/UCF. A highly homogeneous and transparent sodium-zinc-aluminum-silicate glass doped with fluorine and bromine was developed. Glass is transparent from 220 to 2700 nm. It is a crown-type optical glass having refractive index at 587.5 nm nd=1.4959 and Abbe number νd=59.2. This glass shows low dependence of refractive index on temperature dn/dtGlass can withstand multi-kilowatt laser beams. Nonlinear refractive index is the same as for fused silica. Laser damage threshold for 8 ns is about 40 /cm2. This glass becomes a photosensitive one by doping with silver and cerium. It demonstrates refractive index decrement after exposure to UV radiation followed by thermal development and therefore is used for phase volume hologram recording. Spatial modulation of refractive index resulted from precipitation of nano-crystalline phase of sodium fluoride. The main mechanism of refractive index decrement is a photoelastic effect resulted from strong tensions generated in both crystalline and vitreous phases because of difference in their coefficients of thermal expansion. Volume Bragg gratings recorded in this glass, show extremely narrow spectral and angular selectivity and have low losses combined with high tolerance to laser radiation. These gratings possess a unique ability to produce laser beam transformations directly in angular space. This feature paves a way to creation of high power lasers with stable narrow emission spectra and diffraction limited divergence.

  12. On the origin of silicate-bearing diamondites (United States)

    Dobosi, Gabor; Kurat, Gero


    Garnets and clinopyroxenes, intergrown with diamonds in 37 diamondites (“bort”, “polycrystalline diamond aggregates”, “polycrystalline diamond”, “framesite”), presumably from southern Africa, were analyzed for trace element contents by LA-ICP-MS. The intimate diamond-silicate intergrowths suggest that both precipitated from the same fluids during the same crystallization events. In this study we distinguish 5 chemical garnet groups: “peridotitic” (P), intermediate (I) and 3 “eclogitic” groups (E1, E2 and E3). Chondrite-normalized trace element patterns for the garnet groups roughly correlate with major element abundances. Most of P garnets show complex, mildly sinusoidal REEN patterns with relatively flat HREEN-MREEN, a small hump at Sm-Nd and depleted LREEN, and have relatively high contents of Nb, Ta, U, and Th. The REEN abundance patterns of E garnets differ by showing a continuous increase from LREE to HREE and depletion in LREE and highly incompatible elements relative to the P garnets. Of all garnet groups, E3 garnets are the poorest in highly incompatible trace elements and in Mg. Model equilibrium fluids for P garnets suggest crystallization from magnesian carbonate-bearing fluids/melts, which were very rich in incompatible trace elements — similar to kimberlites. Hypothetical equilibrium melts for E1 and E2 garnets are also magnesian and poorer in LREE and highly incompatible elements relative to typical kimberlitic or carbonatitic melts. Fluids that crystallized the P and most of the E garnets have similar mg numbers indicating a peridotitic source for both. The differences in Cr and highly incompatible element contents can be the result of differences in fluid formation and/or evolution rather than different source rock. The positive correlation of Cr2O3 and mg with the abundances of highly incompatible elements in garnets indicate fluid-rock fractionation processes rather than igneous fractional crystallization processes being

  13. Modeling Silicate Weathering for Elevated CO2 and Temperature (United States)

    Bolton, E. W.


    A reactive transport model (RTM) is used to assess CO2 drawdown by silicate weathering over a wide range of temperature, pCO2, and infiltration rates for basalts and granites. Although RTM's have been used extensively to model weathering of basalts and granites for present-day conditions, we extend such modeling to higher CO2 that could have existed during the Archean and Proterozoic. We also consider a wide range of surface temperatures and infiltration rates. We consider several model basalt and granite compositions. We normally impose CO2 in equilibrium with the various atmospheric ranges modeled and CO2 is delivered to the weathering zone by aqueous transport. We also consider models with fixed CO2 (aq) throughout the weathering zone as could occur in soils with partial water saturation or with plant respiration, which can strongly influence pH and mineral dissolution rates. For the modeling, we use Kinflow: a model developed at Yale that includes mineral dissolution and precipitation under kinetic control, aqueous speciation, surface erosion, dynamic porosity, permeability, and mineral surface areas via sub-grid-scale grain models, and exchange of volatiles at the surface. Most of the modeling is done in 1D, but some comparisons to 2D domains with heterogeneous permeability are made. We find that when CO2 is fixed only at the surface, the pH tends toward higher values for basalts than granites, in large part due to the presence of more divalent than monovalent cations in the primary minerals, tending to decrease rates of mineral dissolution. Weathering rates increase (as expected) with increasing CO2 and temperature. This modeling is done with the support of the Virtual Planetary Laboratory.

  14. Removal of lead from cathode ray tube funnel glass by generating the sodium silicate. (United States)

    Hu, Biao; Zhao, Shuangshuang; Zhang, Shuhao


    In the disposal of electronic waste, cathode ray tube (CRT) funnel glass is an environmental problem of old television sets. Removal of the lead from CRT funnel glass can prevent its release into the environment and allow its reuse. In this research, we reference the dry progress productive technology of sodium silicate, the waste CRT glass was dealt with sodium silicate frit melted and sodium silicate frit dissolved. Adding a certain amount of Na ₂CO₃to the waste CRT glass bases on the material composition and content of it, then the specific modulus of sodium silicate frit is obtained by melting progress. The silicon, potassium and sodium compounds of the sodium silicate frit are dissolved under the conditions of high temperature and pressure by using water as solvent, which shows the tendency that different temperature, pressure, liquid-solid ratio and dissolving time have effect on the result of dissolving. At 175°C(0.75MPa), liquid-solid ratio is 1.5:1, the dissolving time is 1h, the dissolution rate of sodium silicate frit is 44.725%. By using sodium sulfide to separate hydrolysis solution and to collect lead compounds in the solution, the recovery rate of lead in dissolving reached 100% and we can get clean sodium silicate and high purity of lead compounds. The method presented in this research can recycle not only the lead but also the sodium, potassium and other inorganic minerals in CRT glass and can obtain the comprehensive utilization of leaded glass.

  15. Polymer/Silicate Nanocomposites Used to Manufacture Gas Storage Tanks With Reduced Permeability (United States)

    Campbell, Sandi G.; Johnston, Chris


    Over the past decade, there has been considerable research in the area of polymer-layered silicate nanocomposites. This research has shown that the dispersion of small amounts of an organically modified layered silicate improves the polymer strength, modulus, thermal stability, and barrier properties. There have been several reports on the dispersion of layered silicates in an epoxy matrix. Potential enhancements to the barrier properties of epoxy/silicate nanocomposites make this material attractive for low permeability tankage. Polymer matrix composites (PMCs) have several advantages for cryogenic storage tanks. They are lightweight, strong, and stiff; therefore, a smaller fraction of a vehicle's potential payload capacity is used for propellant storage. Unfortunately, the resins typically used to make PMC tanks have higher gas permeability than metals. This can lead to hydrogen loss through the body of the tank instead of just at welds and fittings. One approach to eliminate this problem is to build composite tanks with thin metal liners. However, although these tanks provide good permeability performance, they suffer from a substantial mismatch in the coefficient of thermal expansion, which can lead to failure of the bond between the liner and the body of the tank. Both problems could be addressed with polymersilicate nanocomposites, which exhibit reduced hydrogen permeability, making them potential candidates for linerless PMC tanks. Through collaboration with Northrop Grumman and Michigan State University, nanocomposite test tanks were manufactured for the NASA Glenn Research Center, and the helium permeability was measured. An organically modified silicate was prepared at Michigan State University and dispersed in an epoxy matrix (EPON 826/JeffamineD230). The epoxy/silicate nanocomposites contained either 0 or 5 wt% of the organically modified silicate. The tanks were made by filament winding carbon fibers with the nanocomposite resin. Helium permeability

  16. Experimental Investigation of Irradiation-driven Hydrogen Isotope Fractionation in Analogs of Protoplanetary Hydrous Silicate Dust (United States)

    Roskosz, Mathieu; Laurent, Boris; Leroux, Hugues; Remusat, Laurent


    The origin of hydrogen in chondritic components is poorly understood. Their isotopic composition is heavier than the solar nebula gas. In addition, in most meteorites, hydrous silicates are found to be lighter than the coexisting organic matter. Ionizing irradiation recently emerged as an efficient hydrogen fractionating process in organics, but its effect on H-bearing silicates remains essentially unknown. We report the evolution of the D/H of hydrous silicates experimentally irradiated by electrons. Thin films of amorphous silica, amorphous “serpentine,” and pellets of crystalline muscovite were irradiated at 4 and 30 keV. For all samples, irradiation leads to a large hydrogen loss correlated with a moderate deuterium enrichment of the solid residue. The entire data set can be described by a Rayleigh distillation. The calculated fractionation factor is consistent with a kinetically controlled fractionation during the loss of hydrogen. Furthermore, for a given ionizing condition, the deuteration of the silicate residues is much lower than the deuteration measured on irradiated organic macromolecules. These results provide firm evidence of the limitations of ionizing irradiation as a driving mechanism for D-enrichment of silicate materials. The isotopic composition of the silicate dust cannot rise from a protosolar to a chondritic signature during solar irradiations. More importantly, these results imply that irradiation of the disk naturally induces a strong decoupling of the isotopic signatures of coexisting organics and silicates. This decoupling is consistent with the systematic difference observed between the heavy organic matter and the lighter water typically associated with minerals in the matrix of most carbonaceous chondrites.

  17. Physical processes affecting availability of dissolved silicate for diatom production in the Arabian Sea (United States)

    Young, David K.; Kindle, John C.


    A passive tracer to represent dissolved silicate concentrations, with biologically realistic uptake kinetics, is successfully incorporated into a three-dimensional, eddy-resolving, ocean circulation model of the Indian Ocean. Hypotheses are tested to evaluate physical processes which potentially affect the availability of silicate for diatom production in the Arabian Sea. An alternative mechanism is offered to the idea that open ocean upwelling is primarily responsible for the high, vertical nutrient flux and consequent large-scale phytoplankton bloom in the northwestern Arabian Sea during the southwest monsoon. Model results show that dissolved silicate in surface waters available for uptake by diatoms is primarily influenced by the intensity of nearshore upwelling from southwest monsoonal wind forcing and by the offshore advective transport of surface waters. The upwelling, which in the model occurs within 200±50 km of the coast, appears to be a result of a combination of coastal upwelling, Ekman pumping, and divergence of the coastal flow as it turns offshore. Localized intensifications of silicate concentrations appear to be hydrodynamically driven and geographically correlated to coastal topographic features. The absence of diatoms in sediments of the eastern Arabian Basin is consistent with modeled distributional patterns of dissolved silicate resulting from limited westward advection of upwelled coastal waters from the western continental margin of India and rapid uptake of available silicate by diatoms. Concentrations of modeled silicate become sufficiently low to become unavailable for diatom production in the eastern Arabian Sea, a region between 61°E and 70°E at 8°N on the south, with the east and west boundaries converging on the north at ˜67°E, 20°N.

  18. Experimental calibration of a new oxybarometer for silicic magmas based on the partitioning of vanadium between magnetite and silicate melt (United States)

    Arató, Róbert; Audétat, Andreas


    Oxygen fugacity is an important parameter in magmatic systems that affects the stability of mineral phases and fluid species. However, there is no well-established method to reconstruct the oxygen fugacity of slowly cooled magmas such as granite, for example, because existing oxybarometers (e.g., magnetite-ilmenite method) are susceptible to re-equilibration processes during slow cooling and thus lead to erroneous results when applied for granitic rocks. In this study, we aim at developing an oxybarometer that is based on the partitioning of vanadium (a redox-sensitive element) between magnetite inclusions and silicate melt inclusions preserved in quartz phenocrysts, where they were protected from subsolidus alteration and can be measured as entities by LA-ICP-MS. In the first - experimental - part of this study we investigated the effects of temperature (800-950 ° C), pressure (1-2 kbar), oxygen fugacity (from ΔFMQ+0.7 to ΔFMQ+4.0), magnetite composition, and melt composition on the partition coefficient of vanadium between magnetite and melt (DVmgt-melt). The experiments were carried out in cold-seal pressure vessels and the starting material was a mixture of V-doped haplogranite glasses or natural obsidian powder with variable aluminum saturation index (ASI), and synthetic, V-free magnetite of 10-20 μm grain size. The vanadium partition coefficient was found to depend strongly on oxygen fugacity, and to lesser (but still considerable) degrees on melt composition and temperature. A more than 1.5 log unit decrease in DVmgt-melt values with increasing oxygen fugacity can be explained by a change of the dominant valence state of V in the silicate melt. For a given oxygen fugacity buffer DVmgt-melt decreases with increasing temperature, but this reflects mostly the change in absolute fO2 values while the net temperature effect is in fact positive. DVmgt-melt depends significantly on melt composition, resulting in higher D-values with increasing aluminum

  19. Multiple magmatism in an evolving suprasubduction zone mantle wedge: The case of the composite mafic-ultramafic complex of Gaositai, North China Craton (United States)

    Yang, Fan; Santosh, M.; Tsunogae, T.; Tang, Li; Teng, Xueming


    The suprasubduction zone mantle wedge of active convergent margins is impregnated by melts and fluids leading to the formation of a variety of magmatic and metasomatic rock suites. Here we investigate a composite mafic-ultramafic intrusion at Gaositai, in the northern margin of the North China Craton (NCC). The hornblende gabbro-serpentinite-dunite-pyroxenite-gabbro-diorite suite surrounded by hornblendites of this complex has long been considered to represent an ;Alaskan-type; zoned pluton. We present petrologic, mineral chemical, geochemical and zircon U-Pb and Lu-Hf data from the various rock types from Gaositai including hornblende gabbro, serpentinite, dunite, pyroxenite, diorite and the basement hornblendite which reveal the case of multiple melt generation and melt-peridotite interaction. Our new mineral chemical data from the mafic-ultramafic suite exclude an ;Alaskan-type; affinity, and the bulk geochemical features are consistent with subduction-related magmatism with enrichment of LILE (K, Rb, and Ba) and LREE (La and Ce), and depletion of HFSE (Nb, Ta, Zr, and Hf) and HREE. Zircon U-Pb geochronology reveals that the hornblendites surrounding the Gaositai complex are nearly 2 billion years older than the intrusive complex and yield early Paleoproterozoic emplacement ages (2433-2460 Ma), followed by late Paleoproterozoic metamorphism (1897 Ma). The serpentinites trace the history of a long-lived and replenished ancient sub-continental lithospheric mantle with the oldest zircon population dated as 2479 Ma and 1896 Ma, closely corresponding with the ages obtained from the basement rock, followed by Neoproterozoic and Phanerozoic zircon growth. The oldest member in the Gaositai composite intrusion is the dunite that yields emplacement age of 755 Ma, followed by pyroxenite formed through the interaction of slab melt and wedge mantle peridotite at 401 Ma. All the rock suites also carry multiple population of younger zircons ranging in age from Paleozoic to

  20. Geochemical (LA-ICP-MS) investigations of baddeleyite from the Palaeoproterozoic mafic and Palaeozoic alkaline intrusions in the Arctic part of the Baltic shield (United States)

    Drogobuzhskaya, Svetlana; Bayanova, Tamara; Novikov, Andrey


    Baddeleyite is a zirconium dioxide mineral, which is very important, but less common as zircon. While the zircon microelementary composition study is widely applicable, the baddeleyite geochemical features are poorly known. The first data on REE concentrations and distribution in baddeleyite were published in the past century. Baddeleyite is used as a geochronometer for dating mafic and alkaline rocks. It may be noted that the data on its geochemical composition are quite contradictory with a strongly varying Ce anomaly value and absent Eu anomaly in some samples. The new data on the elementary composition of baddeleyite (REE, Hf, U, Th, Y, and Ti) from the Monchegorsk pluton mafic rocks (2.5 Ga) and Kovdor and Vuoriyarvi deposits (380 Ma) was obtained. The sample morphology was studied using an electronic spectroscopy method (Hitachi S-430), and the position of local analysis on baddeleyite crystals was chosen based on analyzed optic images of minerals. The content of REE and other elements was measured using LA-ICP-MS technique on quadrupole mass-spectrometer ELAN 9000 DRC-e (Perkin Elmer) with laser evaporator UP-266 MACRO (New Wave Research) with a wave length of 266 nm for sampling. The laser ablation was made in argon atmosphere in a 35 and 70 μm diameter spot or when scanning to a line with a pulse repetition rate of 10 Hz and pulse energy of 14-15 J/cm2. The device was calibrated using the NIST SRM 612 standard with a REE, U, and Th concentration of about 40 ppm. The baddeleyite from reference rocks of mafic intrusions are characterized by medium concentrations of Hf (0.69-1.9 %), Th (7.6-21.1), REE (50.3-162), U (164-357), Y (5.0-149) ppm for the sample M-2 from Monchegorsk. Another rocks of alkaline intrusions are depleted in Th (0.25-5.9), REE (9.2-103), U (1.8-48.1), Y(2.9-65.9) ppm and Hf (0.20-1.9%) for the sample Bd-400 from Vuoriyarvi and Hf (0.18-1.3 %), Th (0.4-5.2), REE (2.1-17.7), U (4.2-32.6), Y(2.2-68.4) ppm for the samples Bd-300 and Bd-300

  1. Dating sub-20 micron zircons in granulite-facies mafic dikes from SW Montana: a new approach using automated mineralogy and SIMS U-Pb geochronology (United States)

    Ault, A. K.; Mahan, K. H.; Flowers, R. M.; Chamberlain, K.; Appleby, S. K.; Schmitt, A. K.


    Geochronological data is fundamental to all tectonic studies, but a major limitation for many lithologies is a paucity of sizeable zircons suitable for conventional U-Pb techniques. In particular, mafic dike swarms provide important time markers for tectonometamorphic activity in Precambrian terranes, but commonly yield little or no zircon or baddeleyite sufficient for TIMS or standard ion-probe analysis of crystal separates. We apply a new approach involving in-situ automated mineralogy and high spatial resolution Secondary Ion Mass Spectrometry (SIMS) geochronology to a mafic dike swarm exposed in the Northern Madison Range of SW Montana. The dikes cross-cut early fabrics but are also variably deformed and metamorphosed to P-T conditions as high as 1.2 GPa and 850 C. The swarm emplacement age is inferred to be ca. 2.1 Ga based on similarities to dated dikes in the adjacent Tobacco Root Mountains. Resolving the timing of dike emplacement and high-grade metamorphism in the study area is important for understanding the extent of post-Archean modification to the northwest margin of the Wyoming craton. Identification and textural characterization of zircons were facilitated by in-situ automated mineralogical analysis, in contrast to a standard elemental X-ray mapping approach. Our technique uses an SEM-based platform coupling calibrated BSE data with X-ray data collected by multiple energy dispersive spectrometers to rapidly identify target accessory phases at high spatial resolution. Whole thin section search maps were generated in ~30 minutes at 4 µm pixel resolution. Our dike thin sections commonly contained >300 zircons in a variety of textural settings, with 80% having a short dimension dated in-situ by adjusting the field aperture of the CAMECA ims1270 to preferentially collect secondary ions emitted from within the inner few microns of the ~15 µm diameter analysis pit. This allows us to analyze zircon grains with a minimum dimension as small as 8 μm at

  2. Magma storage conditions and differentiation of the mafic Lower Pollara volcanics, Salina Island, Aeolian Islands, Italy: implications for the formation conditions of shoshonites and potassic rocks (United States)

    Beermann, Oliver; Holtz, François; Duesterhoeft, Erik


    Crystallization experiments of basaltic andesite mafic endmember from the 24 ka Lower Pollara eruption (Salina, Aeolian Islands, Italy) were investigated at 200 MPa, 950-1100 °C, in the H2O activity ( aH2O) range 0.3 to 1, and at two ranges of oxygen fugacity ( fO2) between FMQ to FMQ+1 and FMQ+2 to FMQ+3.3 (log bars, FMQ is fayalite-magnetite-quartz). Comparison of the produced phase assemblages and phase compositions with the natural sample reveals that the storage conditions were 1050 °C, 2.8 wt% H2O in the melt ( aH2O 0.5), and relatively oxidizing ( FMQ+2.5). The composition of plagioclase in the groundmass indicates a period of cooling to ≤950 °C. The overall differentiation trends of the Salina volcanics can be explained by fractional crystallization close to H2O saturated conditions ( 5 wt% H2O in the melt at 200 MPa) and most likely by accumulation of plagioclase, i.e., in basaltic andesites, and by various degree of mixing-mingling between the corresponding differentiates. The slightly elevated K2O contents of the most mafic basaltic andesites that can be found in the lowermost unit of the Lower Pollara pyroclastics reveal earlier processes of moderately hydrous fractional crystallization at higher temperature (> 1050 °C). Fractional crystallization with decreasing influence of H2O causes a moderate decrease of MgO and a significant increase of K2O relative to SiO2 in the residual liquids. It is exemplarily shown that the crystallization of SiO2-rich phases at high temperature and low aH2O of only moderately K2O-rich calc-alkaline basalts can produce shoshonitic and high potassic rocks similar to those of Stromboli and Volcano. This suggests that the observed transition from calc-alkaline to shoshonitic and high potassic volcanism at the Aeolian Arc over time can be initiated by a general increase of magmatic temperatures and a decrease of aH2O in response to the extensional tectonics and related increase of heat flow and declining influence of slab

  3. Asbestos and silicate pollution: Public health. July 1976-March 1989 (Citations from Pollution Abstracts). Report for July 1976-March 1989

    Energy Technology Data Exchange (ETDEWEB)


    This bibliography contains citations concerning the occurence and effects of asbestos and silicate pollution as a public health risk. This bibliography covers research on the epidemiological and medical studies involving exposure to asbestos and silicates, ingestion of asbestos, and methods to measure asbestos and silicate pollution. Topics include cancer risks, asbestos in drinking water, hazards of silica dust inahalation, and hazard management and abatement. Asbestos and silicate pollution in the workplace, and asbestos removal technology are found in separate published bibliographies. (Contains 104 citations fully indexed and including a title list.)

  4. The utilization of waste by-products for removing silicate from mineral processing wastewater via chemical precipitation. (United States)

    Kang, Jianhua; Sun, Wei; Hu, Yuehua; Gao, Zhiyong; Liu, Runqing; Zhang, Qingpeng; Liu, Hang; Meng, Xiangsong


    This study investigates an environmentally friendly technology that utilizes waste by-products (waste acid and waste alkali liquids) to treat mineral processing wastewater. Chemical precipitation is used to remove silicate from scheelite (CaWO4) cleaning flotation wastewater and the waste by-products are used as a substitute for calcium chloride (CaCl2). A series of laboratory experiments is conducted to explain the removal of silicate and the characterization and formation mechanism of calcium silicate. The results show that silicate removal reaches 90% when the Ca:Si molar ratio exceeds 1.0. The X-ray diffraction (XRD) results confirm the characterization and formation of calcium silicate. The pH is the key factor for silicate removal, and the formation of polysilicic acid with a reduction of pH can effectively improve the silicate removal and reduce the usage of calcium. The economic analysis shows that the treatment costs with waste acid (0.63 $/m(3)) and waste alkali (1.54 $/m(3)) are lower than that of calcium chloride (2.38 $/m(3)). The efficient removal of silicate is confirmed by industrial testing at a plant. The results show that silicate removal reaches 85% in the recycled water from tailings dam. Copyright © 2017 Elsevier Ltd. All rights reserved.

  5. The microstructure and surface morphology of radiopaque tricalcium silicate cement exposed to different curing conditions. (United States)

    Formosa, L M; Mallia, B; Bull, T; Camilleri, J


    Tricalcium silicate is the major constituent phase in mineral trioxide aggregate (MTA). It is thus postulated that pure tricalcium silicate can replace the Portland cement component of MTA. The aim of this research was to evaluate the microstructure and surface characteristics of radiopaque tricalcium silicate cement exposed to different curing conditions namely at 100% humidity or immersed in either water or a simulated body fluid at 37°C. The materials under study included tricalcium silicate and Portland cements with and without the addition of bismuth oxide radiopacifier. Material characterization was performed on hydrated cements using a combination of scanning electron microscopy (SEM) with X-ray energy dispersive (EDX) analyses and X-ray diffraction (XRD) analyses. Surface morphology was further investigated using optical profilometry. Testing was performed on cements cured at 100% humidity or immersed in either water or Hank's balanced salt solution (HBSS) for 1 and 28 days at 37°C. In addition leachate analysis was performed by X-ray fluorescence of the storage solution. The pH of the storage solution was assessed. All the cements produced calcium silicate hydrate and calcium hydroxide on hydration. Tricalcium silicate showed a higher reaction rate than Portland cement and addition of bismuth oxide seemed to also increase the rate of reaction with more calcium silicate hydrate and calcium hydroxide being produced as demonstrated by SEM and XRD analysis and also by surface deposits viewed by the optical profilometer. Cement immersion in HBSS resulted in the deposition of calcium phosphate during the early stages following immersion and extensive calcification after 28 days. The pH of all storage solutions was alkaline. The immersion in distilled water resulted in a higher pH of the solution than when the cements were immersed in HBSS. Leachate analysis demonstrated high calcium levels in all cements tested with higher levels in tricalcium silicate and

  6. Electrical conduction and glass relaxation in alkali- silicate glasses (United States)

    Angel, Paul William

    Electrical response measurements from 1 Hz to 1 MHz between 50o and 540oC were made on potassium, sodium and lithium-silicate glasses with low alkali oxide contents. Conductivity and electrical relaxation responses for both annealed and air quenched glasses of the same composition were compared. Quenching was found to lower the dc conductivity, σdc, and activation energy as well as increase the pre-exponential term when compared to the corresponding annealed glass of the same composition. All of the glasses exhibited Arrhenius behavior in the log σdc against 1/T plots. A sharp decrease in σdc was observed for glasses containing alkali concentrations of 7 mol% or less. The σdc activation energy exhibited similar behavior when plotted as a function of alkali composition and was explained in terms of a mixture of the weak and strong electrolyte models. The depression angle for fits to the complex impedance data were also measured as a function of thermal history, alkali concentration and alkali species. These results were interpreted in terms of changes in the distribution of relaxation times. Annealed samples from a single melt of a 10 mol% K2O-90SiO2 glass were reheated to temperatures ranging from 450o to 800oC, held isothermally for 20 min, and then quenched in either air or silicon oil. The complex impedance of both an annealed and the quenched samples were then measured as a function of temperature from 120o to 250oC. The σdc was found to be remain unaffected by heat treatments below 450oC, to increase rapidly over an approximate 200oC range of temperatures that was dependent on cooling rate and to be constant for heat treatments above this range. This behavior is interpreted in terms of the mean structural relaxation time as a function of temperature and cooling rate near the glass transition temperature and glass transformation ranges. A more detailed definition for the transition and transformation temperatures and ranges was also provided.

  7. Spin transition in Fe3+ in Mg-silicate perovskite (United States)

    Catalli, K.; Shim, S.; Prakapenka, V. B.; Zhao, J.; Sturhahn, W.; Liu, H.


    In recent years, spin transitions have been reported in both perovskite (Pv) (Badro et al., 2004) and magnesiowüstite (Mw) (Lin et al., 2005). Although no density change has been detected in ferrous iron bearing Pv (Lundin et al., 2008), large changes in density have been found to occur with the spin transition in Mw (Fei et al., 2007). This difference has been attributed to the diverse coordination and oxidation states of Fe in Pv and has made analysis of previous experimental data difficult. We have measured synchrotron Mössbauer spectroscopy (SMS) and X-ray diffraction (XRD) on Mg-silicate Pv with all Fe in Fe3+ (0.9MgSiO3- 0.1Fe2O3) up to 136 GPa in the laser heated diamond anvil cell with an argon pressure medium. Our SMS shows that Fe3+ enters both the dodecahedral and octahedral sites at the entire pressure range we studied (47-136 GPa). We found that both high and low spin Fe3+ exist in the octahedral site between 47 and 63 GPa and then all Fe3+ in the octahedral site becomes low spin at higher pressures, while Fe3+ in the dodecahedral site remains high spin to 136 GPa. Pressure-volume data, measured up to 106 GPa using the gold pressure scale (Tsuchiya, 2003), shows that the spin transition does not effect density but does result in a 10% increase in the bulk modulus near 60 GPa. Below 60 GPa, ferric Pv is 9% more compressible than ferrous Pv, but above 60 GPa, ferric Pv is 17% less compressible than ferrous perovskite. This change in compressibility is likely due to a change in compression mechanism: at low pressure compression is accomplished by a combination of the gradual spin collapse and lattice compression. However, after the spin transition is complete, only lattice compression is at work at higher pressures. If the lower mantle has as much Fe3+ as suggested by McCammon et al. (1997) and Frost et al. (2004), this may result in a global discontinuity at the mid-mantle. If not, local enrichment of Fe3+ can result in a discontinuity, which can be

  8. Rocas Verdes Ophiolite Complexes in the Southernmost Andes: Remnants of the Mafic Igneous Floor of a Back-arc Basin that Rifted the South American Continental Crust in the Late Jurrassic and Early Cretaceous (United States)

    Stern, C. R.


    The Rocas Verdes are an en echelon group of late Jurassic and early Cretaceous igneous complexes in the southernmost Andes. They consist of mafic pillow lavas, dikes and gabbros interpreted as the upper portions of ophiolite complexes formed along mid-ocean-ridge-type spreading centers. When secondary metamorphic affects are accounted for, the geochemistry of mafic Rocas Verdes rocks are similar to ocean-ridge basalts (MORB). The spreading centers that generated the Rocas Verdes rifted the southwestern margin of the Gondwana continental crust, during the start of break-up in the southern Atlantic, to form the igneous floor of a back-arc basin behind a contemporaneous convergent plate boundary magmatic arc. Late Jurassic and early Cretaceous sediments from both the magmatic arc on the southwest and the continental platform on the northeast of the basin were deposited in the Rocas Verdes basin, and these sediments are interbedded with mafic pillow lavas along the margins of the Rocas Verdes mafic complexes. Also, mafic dikes and gabbros intrude older pre-Andean and Andean lithologies along both flanks of the Rocas Verdes, and leucocratic country rocks are engulfed in the Rocas Verdes mafic complexes. These relations indicate that the Rocas Verdes complexes formed in place and are autochthonous, having been uplifted but not obducted, which may explain the lack of exposure of the deeper ultramafic units. Zircon U/Pb ages of 150+/-1 Ma for the Larsen Harbour Formation, a southern extension of the Rocas Verdes belt on South Georgia Island, and 138+/-2 Ma for the Sarmiento complex, the northernmost in the Rocas Verdes belt, indicate that this basin may have formed by "unzipping" from the south to the north, with the southern portion beginning to form earlier and developing more extensively than the northern portion of the basin. Paleomagnetic data suggest that the Rocas Verdes basin developed in conjunction with the displacement of the Antarctic Peninsula and opening of

  9. Through The Looking Glass: New Laboratory Spectra Of Glassy Silicates For The Comparison To Astrophysical Environments (United States)

    Speck, Angela; Whittington, A.; Hofmeister, A.


    Many astrophysical environments exhibit a spectral feature at around 10 microns, which has long been attributed to amorphous silicates, but whose precise nature remains a mystery. Furthermore, the astronomically observed feature varies from location to location, and even within a given object both spatially and temporally. There have been many laboratory studies of potential cosmic dust analogs attempting to determine the exact nature of this dust, but most of those studies have failed to produce laboratory spectra that precisely match the observed astronomical spectra. We present new high-resolution spectra of a selection of silicate glasses whose compositions cover those expected to form in cosmic environments. These include synthetic endmember glasses of major mineral groups such as melilites (akermanite, gehlenite), pyroxenes (enstatite), olivines (forsterite) and silica; glasses produced by remelting natural mineral samples that contain iron and other elements; and a synthetic "cosmic” silicate glass with solar relative abundances of Mg, Si, Ca, Na and Al. Across the compositional range of 12 samples the 10 micron feature changes in peak position by more than a micron, as well as in shape. We discuss the effects of both compositional and structural factors on spectral features in these glassy silicates and we compare our new laboratory glass spectra with synthetic amorphous silicate spectra currently used in most models of dusty astrophysical environments. The synthetic spectra do not match either peak position or shape of any of our glass samples.

  10. Heavily Tm3+-Doped Silicate Fiber for High-Gain Fiber Amplifiers

    Directory of Open Access Journals (Sweden)

    Yin-Wen Lee


    Full Text Available We report on investigation the potential of a 7 wt% (8.35 × 1020 Tm3+/cm3 doped silicate fibers for high-gain fiber amplifiers. Such a high ion concentration significantly reduces the required fiber length of high-power 2 μm fiber laser systems and allows the high-repetition rate operation in 2 μm mode-locked fiber lasers. To evaluate the feasibility of extracting high gain-per-unit-length from this gain medium, we measure several key material properties of the silicate fiber, including the absorption/emission cross-sections, upper-state lifetime, fiber background loss, and photodarkening resistance. We show through numerical simulations that a signal gain-per-unit-length of 3.78 dB/cm at 1950 nm can be achieved in a watt-level core-pumped Tm3+-doped silicate fiber amplifier. In addition, an 18-dB 2013-nm amplifier is demonstrated in a 50-cm 7 wt% Tm3+-doped double-clad silicate fiber. Finally, we experimentally confirm that the reported silicate host exhibits no observable photodarkening.

  11. Partitioning of siderophile elements between metallic liquids and silicate liquids under high-pressure and temperature (United States)

    Nakatsuka, A.; Urakawa, S.


    High-pressure metal-silicate element partitioning studies have shown the possibility that the mantle abundance of siderophile elements is consistent with core-mantle equilibration at high pressures and high temperatures. Equilibrium conditions are, however, still under debates partly due to the uncertainty of partition coefficients, which vary not only with pressure, temperature and oxygen fugacity but also with composition. We have carried out partitioning experiments of siderophile elements between liquid metal and ultramafic silicate liquid at high pressure to evaluate the effects of composition on the partition coefficients. Partitioning experiments were conducted by KAWAI-type high pressure apparatus. We used natural peridotite and Fe alloy as starting materials and they were contained in graphite capsule. The quenched samples were examined by electron microprobe. Quenched textures indicate that metallic melts coexisted with silicate melts during experiment. The metallic melt contained 7-9 wt% of C. Oxygen fugacity varied from IW-3 to IW-1 in associated with the composition of the starting material. At the reduced condition, silicate melt was enriched in SiO2 compared to peridotite because of the oxidation of Si in metallic melts. When oxygen fugacity is close to IW buffur, silicate melt was enriched in FeO due to the oxidation of metallic Fe and it had high NBO/T = 3.5-4. The partition coefficients D for Co, Ni and Fe were dependent on oxygen fugacity as well as the chemical compositions.

  12. Evaluation of the mechanical properties of acetic-cure silicone with the addition of magnesium silicate

    Directory of Open Access Journals (Sweden)

    Ronald Vargas Orellana


    Full Text Available Current study evaluates the mechanical properties (tensile and tear strength of an acetic-cure silicone with the addition of 10 or 20% vol. magnesium silicate. Magnesium silicate was added to the silicone at concentrations of 10 (MS-10 and 20% (MS-20 volume, followed by the analysis of tensile strength, maximal elongation during tensile and tear strength. Results were compared to control group of silicone without additives (CG. Mean rates were determined and compared by analysis of variance and Tukey’s test (p < 0.05. Control group had the greatest elongation when subjected to tensile strength (650%, whereas the MS-10 group statistically showed a better tensile strength (8.8 MPa when compared to CG (7.5 MPa and MS-20 (7.5 MPa groups. Both magnesium silicate groups exhibited statistically similar tear strength, whereas MS-20 group demonstrated statistically greater tear strength. The addition of 10% magnesium silicate increased tensile strength, but tear strength and elongation were similar to control. The addition of 20% magnesium silicate did not affect tensile but increased tear strength.

  13. Trace fossils of Ordovician radiolarian chert and siliceous mudstone in Newfoundland, Canada (United States)

    Kakuwa, Yoshitaka


    Ordovician radiolarian chert and siliceous mudstone in Newfoundland are examined to elucidate the development of trace fossils in and on the Early Paleozoic ocean bottom. Chert sedimentation in the Shoal Arm Formation (SAF) is limited to a short interval, but its sedimentation rate is high with few siliciclastic materials. Trace fossils are common in chert in the SAF, but their development is interrupted by frequent anoxic events. The trace fossils are larger than trace fossils in the contemporary chert of other areas. In contrast, trace fossils in the Strong Island Chert (SIC) are moderately-sized to small, with a few sandstone beds interbedded with chert. Those characteristics reflect differences in the sedimentary environments. Rocks of the SIC were deposited in a basinal part of a back-arc basin; whereas, those in the SAF were deposited on a small isolated basin. Red chert or siliceous rocks that underlie grey cherts and siliceous rocks of the SIC and the SAF bear small and simple trace fossils. This is a common feature of ;oceanic red rocks.; Radiolarian chert and siliceous rocks in Newfoundland also showed that trace fossils are widespread by the Middle Ordovician in the deep-sea environment. The Great Ordovician Biodiversification Event is confirmed in the radiolarian siliceous rocks there.

  14. Antimicrobial activities and cellular responses to natural silicate clays and derivatives modified by cationic alkylamine salts. (United States)

    Hsu, Shan-Hui; Tseng, Hsiang-Jung; Hung, Huey-Shan; Wang, Ming-Chien; Hung, Chiung-Hui; Li, Pei-Ru; Lin, Jiang-Jen


    Nanometer-scale silicate platelet (NSP) materials were previously developed by increasing the interlayer space and exfoliation of layered silicate clays such as montmorillonite and synthetic fluorinated mica by the process of polyamine exfoliation. In this study, the antibacterial activity and cytotoxicity of these nanometer-scale silicate clays were evaluated. The derivatives of NSP (NSP-S) which were modified by C18-fatty amine salts via ionic exchange association exhibited the highest antibacterial activity in the aqueous state among all clays. The high antibacterial activity, however, was accompanied by elevated cytotoxicity. The variations of cell surface markers (CD29 and CD44) and type I collagen expression of fibroblasts treated with the clays were measured to clarify the mechanism of the silicate-induced cytotoxicity. The signal transduction pathway involved the downregulation of extracellular-signal-regulated kinase (ERK), which appeared to participate in silicate-induced cytotoxicity. This study helped to understand the antibacterial potential of NSP and the interaction of natural and modified clays with cellular activities.

  15. Investigation of the physical properties of tricalcium silicate cement-based root-end filling materials. (United States)

    Grech, L; Mallia, B; Camilleri, J


    Tricalcium silicate-based cements have been displayed as suitable root-end filling materials. The physical properties of prototype radiopacified tricalcium silicate cement, Bioaggregate and Biodentine were investigated. Intermediate restorative material was used as a control. The physical properties of a prototype zirconium oxide replaced tricalcium silicate cement and two proprietary cements composed of tricalcium silicate namely Bioaggregate and Biodentine were investigated. Intermediate restorative material (IRM) was used as a control. Radiopacity assessment was undertaken and expressed in thickness of aluminum. In addition the anti-washout resistance was investigated using a novel basket-drop method and the fluid uptake, sorption and solubility were investigated using a gravimetric method. The setting time was assessed using an indentation technique and compressive strength and micro-hardness of the test materials were investigated. All the testing was performed with the test materials immersed in Hank's balanced salt solution. All the materials tested had a radiopacity value higher than 3mm thickness of aluminum. IRM exhibited the highest radiopacity. Biodentine demonstrated a high washout, low fluid uptake and sorption values, low setting time and superior mechanical properties. The fluid uptake and setting time was the highest for Bioaggregate. The addition of admixtures to tricalcium silicate-based cements affects the physical properties of the materials. Copyright © 2012 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  16. Nano porous alkaline earth metal silicates as free fatty acid adsorbents from Crude Palm Oil (CPO) (United States)

    Masmur, Indra; Sembiring, Seri Bima; Bangun, Nimpan; Kaban, Jamaran; Putri, Nabila Karina


    Free fatty acids(FFA) from Crude Palm Oil (CPO) have been adsorbed by alkaline earth metal silicate (M-silicate : M = Mg, Ca, Sr and Ba) adsorbents in ethanol using batch method. The adsorbents were prepared from the chloride salts of alkaline metals and Na2SiO3. The resulting white solid of the alkaline earth metal silicates were then heated at 800°C for 3 hours to enlarge their porosities. All adsorbents were characterized by SEM-EDX, XRD and BET. The EDX spectrum of SEM-EDX showed the appearance of all elements in the adsorbents, and the XRD spectrum of all adsorbents showed that they have crystobalite structure. The porosity of the adsorbents calculated by BET method showed that the porosities of the adsorbents range from 2.0884 - 2.0969 nm. All the adsorbents were used to adsorb the FFA from CPO containing 4.79%, 7.3%, 10.37% and 13.34% of FFA. The ratio of adsorbent to CPO to be used in adsorption of FFA from CPO were made 1:1, 1:2 and 1:3, with adsorption time of 1 hour. We found that the maximum adsorption of FFA from CPO was given by Ca-Silicate adsorbent which was between 69.86 - 94.78%, while the lowest adsorption was shown by Mg-silicate adsorbent which was 49.32 -74.53%.

  17. Dielectric Property of Silicate-Doped CaBi4Ti4O15 Thin Films (United States)

    Ogawa, Shota; Kondoh, Yohta; Kimura, Junichi; Funakubo, Hiroshi; Uchida, Hiroshi


    Thin films of silicate-doped CaBi4Ti4O15 were fabricated to enhance the insulating property of one-axis-oriented CaBi4Ti4O15 films under an applied electric field. The crystalline phase of CaBi4Ti4O15, a type of bismuth layer-structured dielectric (BLSD) compound, was successfully grown on (100)LaNiO3/(111)Pt/TiO2/(100)Si with the preferential orientation of the (001) plane by the addition of bismuth silicate with a nominal composition of Bi12SiO20 up to 1.00%. The crystallographic orientation of the (001)BLSD plane normal to the substrate surface was degraded by excessive bismuth silicate addition above 1.50%. The breakdown electric field was increased by bismuth silicate addition up to 2.00% without the degraded relative dielectric permittivity (ɛr) of approximately 230. The bismuth silicate could precipitate between the grain boundaries in the CaBi4Ti4O15 films without an interface reaction or a solid solution that enhances the insulating behavior of the BLSD films.

  18. Tectonic insights of the southwest Amazon Craton from geophysical, geochemical and mineralogical data of Figueira Branca mafic-ultramafic suite, Brazil (United States)

    Louro, Vinicius H. A.; Cawood, Peter A.; Mantovani, Marta S. M.; Ribeiro, Vanessa B.


    The Figueira Branca Suite is a layered mafic-ultramafic complex in the Jauru Terrane, southwest Amazon Craton. New lithological, geochemical, gamma-ray and potential field data, integrated with geological, isotope and paleomagnetic data are used to characterize this pulse of Mesoproterozoic extension-related magmatism. The Figueira Branca Suite formed through juvenile magma emplacement into the crust at 1425 Ma, coeval with the later stages of the Santa Helena Orogen. Gabbros and peridotite-gabbros display increasing enrichment of LREE, interpreted as evidence of progressive fractionation of the magma. Magnetic and gamma-ray data delimit the extent of magmatism within the suite to four bodies to the north of Indiavaí city. Modelling gravity and magnetic field data indicate that the anomalous sources are close to the surface or outcropping. These intrusions trend northwest over 8 km, with significant remanent magnetization that is consistent with published direction obtained through paleomagnetic data. The emplacement, mineralogy and geochemical signature point towards a back-arc extension tectonic framework in the later stages of the Santa Helena Orogen.

  19. A Low Viscosity Lunar Magma Ocean Forms a Stratified Anorthitic Flotation Crust With Mafic Poor and Rich Units: Lunar Magma Ocean Viscosity

    Energy Technology Data Exchange (ETDEWEB)

    Dygert, Nick [Department of Geological Sciences, Jackson School of Geosciences, University of Texas at Austin, Austin TX USA; Planetary Geosciences Institute, Department of Earth and Planetary Sciences, University of Tennessee, Knoxville, Knoxville TN USA; Lin, Jung-Fu [Department of Geological Sciences, Jackson School of Geosciences, University of Texas at Austin, Austin TX USA; Marshall, Edward W. [Department of Geological Sciences, Jackson School of Geosciences, University of Texas at Austin, Austin TX USA; Kono, Yoshio [HPCAT, Geophysical Laboratory, Carnegie Institution of Washington, Argonne IL USA; Gardner, James E. [Department of Geological Sciences, Jackson School of Geosciences, University of Texas at Austin, Austin TX USA


    Much of the lunar crust is monomineralic, comprising >98% plagioclase. The prevailing model argues the crust accumulated as plagioclase floated to the surface of a solidifying lunar magma ocean (LMO). Whether >98% pure anorthosites can form in a flotation scenario is debated. An important determinant of the efficiency of plagioclase fractionation is the viscosity of the LMO liquid, which was unconstrained. Here we present results from new experiments conducted on a late LMO-relevant ferrobasaltic melt. The liquid has an exceptionally low viscosity of 0.22 $+0.11\\atop{-0.19}$to 1.45 $+0.46\\atop{-0.82}$ Pa s at experimental conditions (1,300–1,600°C; 0.1–4.4 GPa) and can be modeled by an Arrhenius relation. Extrapolating to LMO-relevant temperatures, our analysis suggests a low viscosity LMO would form a stratified flotation crust, with the oldest units containing a mafic component and with very pure younger units. Old, impure crust may have been buried by lower crustal diapirs of pure anorthosite in a serial magmatism scenario.

  20. New constraints on the geochronology and Sm-Nd isotopic characteristics of Bas-Drâa mafic dykes, Anti-Atlas of Morocco (United States)

    El Bahat, Abdelhakim; Ikenne, Moha; Cousens, Brian; Söderlund, Ulf; Ernst, Richard; Klausen, Martin B.; Youbi, Nasrrddine


    The Precambrian inliers of the Anti-Atlas belt across the southern part of Morocco contain numerous mafic dyke and sill swarms, which are thought to represent the erosional remnants of Proterozoic Large Igneous Provinces (LIPs). As part of an extended research campaign to date and characterize these LIPs, two amphiboles from one dyke within the Bas-Drâa inlier (western Anti-Atlas) yielded consistent 40Ar-39Ar ages of 611 Ma ± 1.3; i.e., evidence of magmatic activity during the Ediacaran (635-542 Ma). Furthermore, Nd isotope ratios and model ages identifies four groups of dykes within the Bas-Drâa inlier, all of which were derived from a previously enriched mantle reservoir with very low 143Nd/144Nd ratios (0.51065-0.51170) and corresponding εNd(t) values (-16.44 to -2.45). Such low Nd-ratios arguably reflect either a contribution of crustal components, such as the Paleoproterozoïc schisto-granitic basement, or metasomatic modification of the sub-continental lithospheric mantle.

  1. Dyke-sill relationships in Karoo dolerites as indicators of propagation and emplacement processes of mafic magmas in the shallow crust (United States)

    Coetzee, A.; Kisters, A. F. M.


    This paper describes the spatial and temporal relationships between Karoo-age (ca. 180 Ma) dolerite dykes and a regional-scale saucer-sill complex from the Secunda (coal mine) Complex in the northeastern parts of the Karoo Basin of South Africa. Unlike parallel dyke swarms of regional extensional settings, mafic dykes commonly show curved geometries and highly variable orientations, short strike extents and complex cross-cutting and intersecting relationships. Importantly, the dyke networks originate from the upper contacts of the first-order dolerite sill-saucer structure and are not the feeders of the saucer complex. Cross-cutting relationships indicate the largely contemporaneous formation of dykes and the inner sill and inclined sheets of the underlying saucer. Systematic dykes form a distinct boxwork-type pattern of two high-angle, interconnected dyke sets. The formation and orientation of this dyke set is interpreted to be related to the stretching of roof strata above elongated magma lobes that facilitated the propagation of the inner sill, similar to the ;cracked lid; model described for large saucer complexes in Antarctica. Dyke patterns generally reflect the saucer emplacement process and the associated deformation of wall rocks rather than far-field regional stresses.

  2. Production of biodiesel and lactic acid from rapeseed oil using sodium silicate as catalyst. (United States)

    Long, Yun-Duo; Guo, Feng; Fang, Zhen; Tian, Xiao-Fei; Jiang, Li-Qun; Zhang, Fan


    Biodiesel and lactic acid from rapeseed oil was produced using sodium silicate as catalyst. The transesterification in the presence of the catalyst proceeded with a maximum yield of 99.6% under optimized conditions [3% (w/w) sodium silicate, methanol/oil molar ratio 9/1, reaction time 60 min, reaction temperature 60°C, and stirring rate 250 rpm]. After six consecutive transesterification reactions, the catalyst was collected and used for catalysis of the conversion of glycerol to lactic acid. A maximum yield of 80.5% was achieved when the reaction was carried out at a temperature of 300°C for 90 min. Thus, sodium silicate is an effective catalyst for transesterification and lactic acid production from the biodiesel by-product, glycerol. Copyright © 2011 Elsevier Ltd. All rights reserved.

  3. Eu-, Tb-, and Dy-Doped Oxyfluoride Silicate Glasses for LED Applications

    DEFF Research Database (Denmark)

    Zhu, C.F.; Wang, J.; Zhang, M.M.


    Luminescence glass is a potential candidate for the light-emitting diodes (LEDs) applications. Here, we study the structural and optical properties of the Eu-, Tb-, and Dy-doped oxyfluoride silicate glasses for LEDs by means of X-ray diffraction, photoluminescence spectra, Commission Internationale...... de L’Eclairage (CIE) chromaticity coordinates, and correlated color temperatures (CCTs). The results show that the white light emission can be achieved in Eu/Tb/Dy codoped oxyfluoride silicate glasses under excitation by near-ultraviolet light due to the simultaneous generation of blue, green, yellow......, and red-light wavelengths from Tb, Dy, and Eu ions. The optical performances can be tuned by varying the glass composition and excitation wavelength. Furthermore, we observed a remarkable emission spectral change for the Tb3+ single-doped oxyfluoride silicate glasses. The 5D3 emission of Tb3+ can...

  4. Development of Biomedical Polymer-Silicate Nanocomposites: A Materials Science Perspective (United States)

    Wu, Chia-Jung; Gaharwar, Akhilesh K.; Schexnailder, Patrick J.; Schmidt, Gudrun


    Biomedical polymer-silicate nanocomposites have potential to become critically important to the development of biomedical applications, ranging from diagnostic and therapeutic devices, tissue regeneration and drug delivery matrixes to various bio-technologies that are inspired by biology but have only indirect biomedical relation. The fundamental understanding of polymer-nanoparticle interactions is absolutely necessary to control structure-property relationships of materials that need to work within the chemical, physical and biological constraints required by an application. This review summarizes the most recent published strategies to design and develop polymer-silicate nanocomposites (including clay based silicate nanoparticles and bioactive glass nanoparticles) for a variety of biomedical applications. Emerging trends in bio-technological and biomedical nanocomposites are highlighted and potential new fields of applications are examined.

  5. Electrophoretic deposition of magnesium silicates on titanium implants: Ion migration and silicide interfaces

    Energy Technology Data Exchange (ETDEWEB)

    Afshar-Mohajer, M. [Center for Advanced Manufacturing and Material Processing, Department of Mechanical Engineering, Faculty of Engineering, University of Malaya, Kuala Lumpur 50603 (Malaysia); Yaghoubi, A., E-mail: [Center for High Impact Research, University of Malaya, Kuala Lumpur 50603 (Malaysia); Ramesh, S., E-mail: [Center for Advanced Manufacturing and Material Processing, Department of Mechanical Engineering, Faculty of Engineering, University of Malaya, Kuala Lumpur 50603 (Malaysia); Bushroa, A.R.; Chin, K.M.C.; Tin, C.C. [Center for Advanced Manufacturing and Material Processing, Department of Mechanical Engineering, Faculty of Engineering, University of Malaya, Kuala Lumpur 50603 (Malaysia); Chiu, W.S. [Low Dimensional Materials Research Center, Department of Physics, University of Malaya, Kuala Lumpur 50603 (Malaysia)


    Magnesium silicates (Mg{sub x}SiO{sub y}) and in particular forsterite (Mg{sub 2}SiO{sub 4}) owing to their low thermal expansion mismatch with metals are promising materials for bioactive coating of implants. Here, we report the electrophoretic deposition (EPD) of forsterite onto titanium substrates using different precursors. Unlike bulk samples which achieve full stoichiometry only beyond 1400 °C, non-stoichiometric magnesium silicate rapidly decomposes into magnesium oxide nanowires during sintering. Elemental mapping and X-ray diffraction suggest that oxygen diffusion followed by ion exchange near the substrate leads to formation of an interfacial Ti{sub 5}Si{sub 3} layer. Pre-annealed forsterite powder on the other hand shows a comparatively lower diffusion rate. Overall, magnesium silicate coatings do not exhibit thermally induced microcracks upon sintering as opposed to calcium phosphate bioceramics which are currently in use.

  6. Determine the compressive strength of calcium silicate bricks by combined nondestructive method. (United States)

    Brozovsky, Jiri


    The paper deals with the application of combined nondestructive method for assessment of compressive strength of calcium silicate bricks. In this case, it is a combination of the rebound hammer method and ultrasonic pulse method. Calibration relationships for determining compressive strength of calcium silicate bricks obtained from nondestructive parameter testing for the combined method as well as for the L-type Schmidt rebound hammer and ultrasonic pulse method are quoted here. Calibration relationships are known for their close correlation and are applicable in practice. The highest correlation between parameters from nondestructive measurement and predicted compressive strength is obtained using the SonReb combined nondestructive method. Combined nondestructive SonReb method was proved applicable for determination of compressive strength of calcium silicate bricks at checking tests in a production plant and for evaluation of bricks built in existing masonry structures.

  7. Investigation of the hydration and bioactivity of radiopacified tricalcium silicate cement, Biodentine and MTA Angelus. (United States)

    Camilleri, Josette; Sorrentino, François; Damidot, Denis


    Novel root-end filling materials are composed of tricalcium silicate (TCS) and radiopacifier as opposed to the traditional mineral trioxide aggregate (MTA) which is made up of clinker derived from Portland cement and bismuth oxide. The aim of this research was to characterize and investigate the hydration of a tricalcium silicate-based proprietary brand cement (Biodentine™) and a laboratory manufactured cement made with a mixture of tricalcium silicate and zirconium oxide (TCS-20-Z) and compare their properties to MTA Angelus™. The materials investigated included a cement containing 80% of TCS and 20% zirconium oxide (TCS-20-Z), Biodentine™ and MTA Angelus™. The specific surface area and the particle size distribution of the un-hydrated cements and zirconium oxide were investigated using a gas adsorption method and scanning electron microscopy. Un-hydrated cements and set materials were tested for mineralogy and microstructure, assessment of bioactivity and hydration. Scanning electron microscopy, X-ray energy dispersive analysis, X-ray fluorescence spectroscopy, X-ray diffraction, Rietveld refined X-ray diffraction and calorimetry were employed. The radiopacity of the materials was investigated using ISO 6876 methods. The un-hydrated cements were composed of tricalcium silicate and a radiopacifier phase; zirconium oxide for both Biodentine™ and TCS-20-Z whereas bismuth oxide for MTA Angelus™. In addition Biodentine™ contained calcium carbonate particles and MTA Angelus™ exhibited the presence of dicalcium silicate, tricalcium aluminate, calcium, aluminum and silicon oxides. TCS and MTA Angelus™ exhibited similar specific surface area while Biodentine™ had a greater specific surface area. The cements hydrated and produced some hydrates located either as reaction rim around the tricalcium silicate grain or in between the grains at the expense of volume containing the water initially present in the mixture. The rate of reaction of tricalcium

  8. Metal-Silicate Partitioning of Tungsten from 10 to 50 GPa (United States)

    Shofner, G. A.; Campbell, A. J.; Danielson, L.; Rahman, Z.; Righter, K.


    Geochemical models of core formation are commonly based on core and mantle abundances of siderophile elements that partitioned between silicate and metal in a magma ocean in the early Earth. Tungsten is a moderately siderophile element that may provide constraints on the pressure, temperature, composition, and oxygen fugacity conditions, and on the timing of core formation in the Earth. Previous experimental studies suggest that pressure exerts little to no influence over W metal-silicate partitioning up to 24 GPa, and indicate that the stronger influences are temperature, composition, and oxygen fugacity. However, core formation models based in part on W, predict metal-silicate equilibration pressures outside the available experimental pressure range, requiring extrapolation of parameterized models. Therefore, higher pressure experimental data on W were needed to constrain this important parameter.

  9. The opportunity of silicate product manufacturing with simultaneous pig iron reduction from slag technogenic formations (United States)

    Sheshukov, O. Yu.; Lobanov, D. A.; Mikheenkov, M. A.; Nekrasov, I. V.; Egiazaryan, D. K.


    There are two main kinds of slag in modern steelmaking industry: the electric arc furnace slag (EAF slag) and ladle furnace slag (LF slag). The all known slag processing schemes provide the iron-containing component reduction while silicate component stays unprocessed. On the contrary, the silicate processing schemes doesn't provide the utilization of the iron-containing component. The present-day situation doesn't solve the problem of total slag utilization. The aim of this work is to investigate the opportunity of silicate product obtaining with simultaneous pig iron reduction from EAF and LF slags. The tests are conducted by the method of simplex-lattice design. The test samples are heated and melted under reductive conditions, slowly cooled and then analyzed by XRD methods. The experiment results prove the opportunity: the Portland clinker and pig iron can be simultaneously produced on the basis of these slags with a limestone addition.

  10. Low availability of aluminum in formulations for parenteral nutrition containing silicate. (United States)

    Bohrer, Denise; Bortoluzzi, Fabiana; do Nascimento, Paulo Cícero; de Carvalho, Leandro Machado; de Oliveira, Sandra Ribeiro


    Silicate (Si) and aluminum (Al) may be concomitant impurities in solutions for parenteral nutrition (PN). Silicate can bind to Al to form stable hydroxyaluminosilicates (HAS), thus reducing Al availability. This possibility is investigated by heating solutions containing constituents of PN in glass containers to promote the release of Si and Al. The total amount of Si and Al in solution is measured by atomic absorption spectrometry, and the Al not bound to Si is evaluated by reaction with morin. When the Si:Al molar ratio is >5, no free Al is found in solution. For ratios 5, there is a "residual" fraction of free Al in amino acid formulations. The concomitant presence of Al and Si in solutions for PN reduces the amount of Al available attributable to the formation of HAS. In amino acid formulations this effect may be slightly reduced given the affinity of certain amino acids for Al. Therefore, amino acids may behave in the same fashion as silicate.

  11. Development of Biomedical Polymer-Silicate Nanocomposites: A Materials Science Perspective

    Directory of Open Access Journals (Sweden)

    Chia-Jung Wu


    Full Text Available Biomedical polymer-silicate nanocomposites have potential to become critically important to the development of biomedical applications, ranging from diagnostic and therapeutic devices, tissue regeneration and drug delivery matrixes to various bio-technologies that are inspired by biology but have only indirect biomedical relation. The fundamental understanding of polymer-nanoparticle interactions is absolutely necessary to control structure-property relationships of materials that need to work within the chemical, physical and biological constraints required by an application. This review summarizes the most recent published strategies to design and develop polymer-silicate nanocomposites (including clay based silicate nanoparticles and bioactive glass nanoparticles for a variety of biomedical applications. Emerging trends in bio-technological and biomedical nanocomposites are highlighted and potential new fields of applications are examined.

  12. Li+ alumino-silicate ion source development for the Neutralized Drift Compression Experiment (NDCX)

    Energy Technology Data Exchange (ETDEWEB)

    Roy, Prabir K.; Greenway, Wayne G.; Kwan, Joe W.; Seidl, Peter A.; Waldron, William L.; Wu, James K.


    We report results on lithium alumino-silicate ion source development in preparation for warmdense-matter heating experiments on the new Neutralized Drift Compression Experiment (NDCXII). The practical limit to the current density for a lithium alumino-silicate source is determined by the maximum operating temperature that the ion source can withstand before running into problems of heat transfer, melting of the alumino-silicate material, and emission lifetime. Using small prototype emitters, at a temperature of ~;;1275 oC, a space-charge-limited Li+ beam current density of J ~;;1 mA/cm2 was obtained. The lifetime of the ion source was ~;;50 hours while pulsing at a rate of 0.033 Hz with a pulse duration of 5-6 mu s.

  13. Synergistic effect of silicate clay and phosphazene-oxyalkyleneamines on thermal stability of cured epoxies. (United States)

    Chen, Yu-Min; Liao, Yi-Lin; Lin, Jiang-Jen


    Amine substitution of hexachlorocyclophosphazene (HCP) with poly(oxypropylene)diamines (POP) afforded HCP-POP adducts which were subsequently intercalated into a layered silicate clay. The relative thermal stabilities of the epoxies cured with the phosphazene-amines and the intercalated clays were studied. The organoclays, with the confined HCP-POP from 400 and 2000 g/mol M(w) amines, are nongelled products when using 1/6 M ratio of HCP/POP starting materials in tetrahydrofuran solvent. The intercalation of HCP-POP polyamine salts into sodium montmorillonite afforded the HCP-POP-embedded organoclays with an expanded interlayer silicate spacing (2.4-5.1 nm) from the original 1.2 nm spacing (X-ray diffraction). The effect of silicate clays was evaluated by blending the HCP-POP/clay hybrids into a two-component epoxy system (diglycidyl ether of 4,4'-isopropylidenediphenol (BPA) and a diamine) and fully cured to form solid materials. The distribution of the exfoliated silicate platelets in the matrix was analyzed by transmission electronic microscopy (TEM). Thermal gravimetric analysis (TGA) indicated an enhanced thermal stability for the HCP/clay epoxy nanocomposites, with a delayed weight-loss pattern (temperature of weight loss at 10% (T(10 wt.%)) from 360 to 385 degrees C and temperature of weight loss at 85% (T(85 wt.%)) from 598 to 696 degrees C), compared to the pristine epoxies. By comparing these epoxies with different amounts of phosphazene and/or silicates, the TGA revealed a synergistic effect for the presence of both phosphorous and silicate components. Furthermore, the epoxies had improved physical properties such as hardness (from 3H to 5H) and surface adhesion (observed by scanning electron microscope (SEM) on fracture surface). 2009. Published by Elsevier Inc. All rights reserved.

  14. Through The Looking Glass: The Causes Of Variations In "Amorphous” Silicate Spectral Features. (United States)

    Speck, Angela; Hofmeister, A. M.; Whittington, A. G.


    Silicate dust plays an essential role in many astrophysical environments. The "amorphous” silicate spectral features have been observed in our solar system, young stellar objects, star formation regions, novae, and the diffuse and dense interstellar medium as well as in extragalactic environments such as quasars and AGN. This dust contributes to the physical processes inherent in star formation processes, as well as to several aspects of interstellar processes such as gas heating and the formation of molecules. The discovery of this almost ubiquitous 10um silicate feature, led to many laboratory studies of potential cosmic dust analogs attempting to determine the exact nature of this dust. However, these various lab studies have produced inconsistent and often conflicting results. Studies of ostensibly the same material produce different spectra, which can be attributed to small differences in samples and techniques, but which leave astronomers at a loss as to interpretation of astrophysical data. We survey the compositional and structural factors that affect spectral features in "amorphous” silicates, illustrated with examples of new high-resolution spectra and previously published spectra of amorphous silicates nominally corresponding in composition to the mineral end-members forsterite (Mg2SiO4), enstatite (MgSiO3) and gehlenite (Ca2Al2SiO7). These examples highlight the sensitivity of such characteristics as peak shape, peak position, and the ratio of the 10µm and 18µm features, to subtle compositional / structural variations. By careful laboratory study, we can harness these effects on the spectral features of amorphous silicates to understand dust composition more precisely and provide a rich source of information on dust formation and processing.

  15. Silicates Eroded under Simulated Martian Conditions Effectively Kill Bacteria-A Challenge for Life on Mars. (United States)

    Bak, Ebbe N; Larsen, Michael G; Moeller, Ralf; Nissen, Silas B; Jensen, Lasse R; Nørnberg, Per; Jensen, Svend J K; Finster, Kai


    The habitability of Mars is determined by the physical and chemical environment. The effect of low water availability, temperature, low atmospheric pressure and strong UV radiation has been extensively studied in relation to the survival of microorganisms. In addition to these stress factors, it was recently found that silicates exposed to simulated saltation in a Mars-like atmosphere can lead to a production of reactive oxygen species. Here, we have investigated the stress effect induced by quartz and basalt abraded in Mars-like atmospheres by examining the survivability of the three microbial model organisms Pseudomonas putida, Bacillus subtilis, and Deinococcus radiodurans upon exposure to the abraded silicates. We found that abraded basalt that had not been in contact with oxygen after abrasion killed more than 99% of the vegetative cells while endospores were largely unaffected. Exposure of the basalt samples to oxygen after abrasion led to a significant reduction in the stress effect. Abraded quartz was generally less toxic than abraded basalt. We suggest that the stress effect of abraded silicates may be caused by a production of reactive oxygen species and enhanced by transition metal ions in the basalt leading to hydroxyl radicals through Fenton-like reactions. The low survivability of the usually highly resistant D. radiodurans indicates that the effect of abraded silicates, as is ubiquitous on the Martian surface, would limit the habitability of Mars as well as the risk of forward contamination. Furthermore, the reactivity of abraded silicates could have implications for future manned missions, although the lower effect of abraded silicates exposed to oxygen suggests that the effects would be reduced in human habitats.

  16. Silicates Eroded under Simulated Martian Conditions Effectively Kill Bacteria—A Challenge for Life on Mars (United States)

    Bak, Ebbe N.; Larsen, Michael G.; Moeller, Ralf; Nissen, Silas B.; Jensen, Lasse R.; Nørnberg, Per; Jensen, Svend J. K.; Finster, Kai


    The habitability of Mars is determined by the physical and chemical environment. The effect of low water availability, temperature, low atmospheric pressure and strong UV radiation has been extensively studied in relation to the survival of microorganisms. In addition to these stress factors, it was recently found that silicates exposed to simulated saltation in a Mars-like atmosphere can lead to a production of reactive oxygen species. Here, we have investigated the stress effect induced by quartz and basalt abraded in Mars-like atmospheres by examining the survivability of the three microbial model organisms Pseudomonas putida, Bacillus subtilis, and Deinococcus radiodurans upon exposure to the abraded silicates. We found that abraded basalt that had not been in contact with oxygen after abrasion killed more than 99% of the vegetative cells while endospores were largely unaffected. Exposure of the basalt samples to oxygen after abrasion led to a significant reduction in the stress effect. Abraded quartz was generally less toxic than abraded basalt. We suggest that the stress effect of abraded silicates may be caused by a production of reactive oxygen species and enhanced by transition metal ions in the basalt leading to hydroxyl radicals through Fenton-like reactions. The low survivability of the usually highly resistant D. radiodurans indicates that the effect of abraded silicates, as is ubiquitous on the Martian surface, would limit the habitability of Mars as well as the risk of forward contamination. Furthermore, the reactivity of abraded silicates could have implications for future manned missions, although the lower effect of abraded silicates exposed to oxygen suggests that the effects would be reduced in human habitats. PMID:28955310

  17. Hydration characteristics of calcium silicate cements with alternative radiopacifiers used as root-end filling materials. (United States)

    Camilleri, Josette


    Mineral trioxide aggregate (MTA) is composed of calcium silicate cement and bismuth oxide added for radiopacity. The bismuth oxide in MTA has been reported to have a deleterious effect on the physical and chemical properties of the hydrated material. This study aimed to investigate the hydration mechanism of calcium silicate cement loaded with different radiopacifiers for use as a root-end filling material. Calcium silicate cement loaded with barium sulfate, gold, or silver/tin alloy was hydrated, and paste microstructure was assessed after 30 days. In addition, atomic ratio plots of Al/Ca versus Si/Ca and S/Ca and Al/Ca were drawn, and X-ray energy dispersive analysis of the hydration products was performed to assess for inclusion of heavy metals. The leachate produced from the cements after storage of the cements in water for 28 days and the leaching of the radiopacifiers in an alkaline solution was assessed by using inductively coupled plasma. The hydrated calcium silicate cement was composed of calcium silicate hydrate, calcium hydroxide, ettringite, and monosulfate. Unhydrated cement particles were few. No heavy metals were detected in the calcium silicate hydrate except for the bismuth in MTA. Calcium was leached out early in large quantities that reduced with time. The barium and bismuth were leached in increasing amounts. Copper was the most soluble in alkaline solution followed by bismuth and barium in smaller amounts. The bismuth oxide can be replaced by other radiopacifiers that do not affect the hydration mechanism of the resultant material. Copyright (c) 2010 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  18. Effect of phase composition of calcium silicate phosphate component on properties of brushite based composite cements

    Energy Technology Data Exchange (ETDEWEB)

    Sopcak, T., E-mail: [Institute of Materials Research of SAS, Watsonova 47, 04001 Kosice (Slovakia); Medvecky, L.; Giretova, M.; Stulajterova, R.; Durisin, J. [Institute of Materials Research of SAS, Watsonova 47, 04001 Kosice (Slovakia); Girman, V. [Institute of Physics, Faculty of Science, P. J. Šafárik University, Park Angelinum 9, 04001 Kosice (Slovakia); Faberova, M. [Institute of Materials Research of SAS, Watsonova 47, 04001 Kosice (Slovakia)


    The composite cement mixtures were prepared by mixing brushite (B) with, the amorphous hydrated calcium silicate phosphate (CSPH) or annealed calcium silicate phosphate (CSP composed of Si-saturated hydroxyapatite, wollastonite and silica) phases and water as liquid component. The contents of the silicate-phosphate phase in composites were 10.30 and 50 wt%. The significant effect of both the Ca/P ratio and different solubility of calcium silicate phosphate component in starting cement systems on setting time and phase composition of the final composite cements was demonstrated. The compressive strength of the set cements increased with the filler addition and the highest value (~ 48 MPa) exhibited the 50CSP/B cement composite. The final setting times of the composite cements decreased with the CSPH addition from about 25 to 17 min in 50CSHP/B and setting time of CSP/B composites was around 30 min. The higher content of silica in cements caused the precipitation of fine hydroxyapatite particles in the form of nanoneedles or thin plates perpendicularly oriented to sample surface. The analysis of in vitro cement cytotoxicity demonstrated the strong reduction in cytotoxicity of 10CSPH/B composite with time of cultivation (a low cytotoxicity after 9 days of culture) contrary to cements with higher calcium silicate-phosphate content. These results were attributed to the different surface topography of composite substrates and possible stimulation of cell proliferation by the slow continuously release of ions from 10CSPH/B cement. - Highlights: • Ca/P ratio and solubility of calcium silicate-phosphate components affect the self-setting properties of cements. • Strong relationship between the composite in vitro cytotoxicity and surface microtopography was demonstrated. • Plate-like morphology of coarser particles allowed cells to better adhere and proliferate as compared with nanoneedles.

  19. Preparation and properties of isotropic Nd-Fe-B bonded magnets with sodium silicate binder

    Energy Technology Data Exchange (ETDEWEB)

    Liu, W.Q.; Hu, R.J.; Yue, M., E-mail:; Yin, Y.X.; Zhang, D.T.


    Graphical abstract: To improve the working temperature of bonded Nd-Fe-B magnets, the heat-resistant binder, sodium silicate, was used to prepare new type bonded Nd-Fe-B magnets. The three-dimensional Si-O-Si structure formed in the curing process has excellent strength; it can ensure that the bonded magnets have a certain shape and usable magnetic properties when working at 200 °C. - Highlights: • Sodium silicate enables bonded Nd-Fe-B magnets to be used for higher operation temperatures. • The sodium silicate bonded magnets exhibit usable maximum energy product of 4.057 MGOe at 200 °C. • The compressive strength of sodium silicate bonded magnets is twice bigger than that of epoxy resin bonded magnets. - Abstract: In present study, sodium silicate, a kind of heat-resistant binder, was used to prepare bonded Nd-Fe-B magnets with improved thermal stability and mechanical strength. Effect of curing temperature and curing time of the new binder to the magnetic properties, microstructure, and mechanical strength of the magnets was systematically investigated. Fracture surface morphology observation show that sodium silicate in bonded magnets could completely be cured at 175 °C for 40 min, and the magnets prepared under this condition exhibit optimal properties. They exhibit usable magnetic properties of B{sub r} of 4.66 kGs, H{sub cj} of 4.84 kOe, and (BH){sub max} of 4.06 MGOe at 200 °C. Moreover, the magnets possess high compressive strength of 63 MPa.

  20. The inhibitory effects of potassium chloride versus potassium silicate application on (137)Cs uptake by rice. (United States)

    Fujimura, Shigeto; Yoshioka, Kunio; Ota, Takeshi; Ishikawa, Tetsuya; Sato, Makoto; Satou, Mutsuto


    After the accident at the Fukushima Dai-ichi Nuclear Power Plant owned by the Tokyo Electric Power Company on 11 March 2011, potassium fertilizer was applied to agricultural fields in the southern Tohoku and northern Kanto regions of Japan to reduce the uptake of radiocesium by crops. In this study, we examined the effects of two types of potassium fertilizers, potassium chloride (a readily available potassium fertilizer) and potassium silicate (a slow-release potassium fertilizer), as well as a split application of potassium, on the accumulation of (137)Cs by rice plants in two pot experiments. The (137)Cs concentrations in the brown rice and in the above-ground plants were significantly lower after potassium chloride application than after potassium silicate application. The potassium ion (K(+)) concentrations in soil solutions sampled 9 and 21 d after transplanting were significantly higher for the potassium chloride application than for the potassium silicate application. The K(+) concentrations in soil solutions observed in the application of potassium silicate were similar to those in the treatment when no potassium was applied. This finding indicates that the application of potassium silicate did not sufficiently increase the available K(+) for rice plants in the soil, which led to a greater uptake of (137)Cs after the potassium silicate application than after the application of potassium chloride. The (137)Cs concentration in brown rice was higher in the split application of potassium fertilizer with the second application at the full heading stage than that without split application and the split application with the second application before heading. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Silicates Eroded under Simulated Martian Conditions Effectively Kill Bacteria—A Challenge for Life on Mars

    Directory of Open Access Journals (Sweden)

    Ebbe N. Bak


    Full Text Available The habitability of Mars is determined by the physical and chemical environment. The effect of low water availability, temperature, low atmospheric pressure and strong UV radiation has been extensively studied in relation to the survival of microorganisms. In addition to these stress factors, it was recently found that silicates exposed to simulated saltation in a Mars-like atmosphere can lead to a production of reactive oxygen species. Here, we have investigated the stress effect induced by quartz and basalt abraded in Mars-like atmospheres by examining the survivability of the three microbial model organisms Pseudomonas putida, Bacillus subtilis, and Deinococcus radiodurans upon exposure to the abraded silicates. We found that abraded basalt that had not been in contact with oxygen after abrasion killed more than 99% of the vegetative cells while endospores were largely unaffected. Exposure of the basalt samples to oxygen after abrasion led to a significant reduction in the stress effect. Abraded quartz was generally less toxic than abraded basalt. We suggest that the stress effect of abraded silicates may be caused by a production of reactive oxygen species and enhanced by transition metal ions in the basalt leading to hydroxyl radicals through Fenton-like reactions. The low survivability of the usually highly resistant D. radiodurans indicates that the effect of abraded silicates, as is ubiquitous on the Martian surface, would limit the habitability of Mars as well as the risk of forward contamination. Furthermore, the reactivity of abraded silicates could have implications for future manned missions, although the lower effect of abraded silicates exposed to oxygen suggests that the effects would be reduced in human habitats.

  2. Silicate fertilization of tropical soils: silicon availability and recovery index of sugarcane

    Directory of Open Access Journals (Sweden)

    Mônica Sartori de Camargo


    Full Text Available Sugarcane is considered a Si-accumulating plant, but in Brazil, where several soil types are used for cultivation, there is little information about silicon (Si fertilization. The objectives of this study were to evaluate the silicon availability, uptake and recovery index of Si from the applied silicate on tropical soils with and without silicate fertilization, in three crops. The experiments in pots (100 L were performed with specific Si rates (0, 185, 370 and 555 kg ha-1 Si, three soils (Quartzipsamment-Q, 6 % clay; Rhodic Hapludox-RH, 22 % clay; and Rhodic Acrudox-RA, 68 % clay, with four replications. The silicon source was Ca-Mg silicate. The same Ca and Mg quantities were applied to all pots, with lime and/or MgCl2, when necessary. Sugarcane was harvested in the plant cane and first- and second-ratoon crops. The silicon rates increased soil Si availability and Si uptake by sugarcane and had a strong residual effect. The contents of soluble Si were reduced by harvesting and increased with silicate application in the following decreasing order: Q>RH>RA. The silicate rates promoted an increase in soluble Si-acetic acid at harvest for all crops and in all soils, except RA. The amounts of Si-CaCl2 were not influenced by silicate in the ratoon crops. The plant Si uptake increased according to the Si rates and was highest in RA at all harvests. The recovery index of applied Si (RI of sugarcane increased over time, and was highest in RA.

  3. Corrosion of low Si-alloyed steels in aqueous solution at 90 deg. C. Inhibitive action of silicates; Corrosion d'aciers faiblement allies au silicium en solution aqueuse a 90 deg. C. Action inhibitrice des silicates

    Energy Technology Data Exchange (ETDEWEB)

    Giordana, S


    Low-Si alloyed steels, with Si content ranging from 0.25 to 3.2 wt%, as potential candidate materials for high-level nuclear waste disposal containers, have been studied four the point of view of their corrosion behaviour at 90 deg C in an aqueous solution simulating groundwater (0.1 M NaCl borate-buffered solution with a pH of 8.5) both in reducing and in aerated conditions. The influence of silicate addition to the solution is examined so as to represent the silicon of groundwater, coming from the clay dissolution. When no silicate was added to the solution, silicon as an alloying element was proved to degrade in the first moments the steel ability to passivate. For longer immersion times, protective effects developed most efficiently on the steel containing 3.2 wt% silicon both in reducing an in aerating conditions, Infrared spectroscopy, EDSX, XRD and Raman microprobe were applied to characterise the oxide layer composition, which was found to be a mixture of magnetite and maghemite. In the presence of silicate in the solution, clay-like iron silicates appeared in the corrosion layer. Electrochemical tests results show that adding silicate into solution resulted in increasing the steel ability to passivate. In the short term, the inhibiting effect of silicate was confirmed by mass loss tests, but the tendency was inverse in the long term. Silicate iron layers were eventually less protective than the magnetite layers formed in the absence of silicate. (author)

  4. Influence of Chemical Conditions on the Nanoporous Structure of Silicate Aerogels

    Directory of Open Access Journals (Sweden)

    Katalin Sinkó


    Full Text Available Silica or various silicate aerogels can be characterized by highly porous, open cell, low density structures. The synthesis parameters influence the three-dimensional porous structures by modifying the kinetics and mechanism of hydrolysis and condensation processes. Numerous investigations have shown that the structure of porous materials can be tailored by variations in synthesis conditions (e.g., the type of precursors, catalyst, and surfactants; the ratio of water/precursor; the concentrations; the medium pH; and the solvent. The objectives of this review are to summarize and elucidate the effects of chemical conditions on the nanoporous structure of sol-gel derived silicate aerogels.

  5. Inorganic polymer cement from Fe-Silicate glasses: Varying the activating solution to glass ratio


    Machiels, Lieven; Arnout, Lukas; Jones , Peter Tom; Blanpain, Bart; Pontikes, Yiannis


    Large volumes of Fe-silicate glasses - slags - are produced as residues of metal production and waste treatment processes. It would be interesting if these materials could become an alternative group of precursors for the synthesis of inorganic polymer (IP) cements. This paper investigates the polymerisation of Fe-silicate glasses of composition (in wt%) SiO2: 40; FeO: 30; CaO: 15; Al2O3: 8 and an activating solution of composition (in wt%) Na2O: 15; SiO2: 13; H2O: 72. The mass ratio of the a...

  6. The LithicUB project: A virtual lithotheque of siliceous rocks at the University of Barcelona

    Directory of Open Access Journals (Sweden)

    Marta Sánchez


    Full Text Available The LithicUB project began in 2009 with two main objectives. The first objective was to make available to the scientific community the description and classification of a set of siliceous rocks that had been recovered from different surveys. The second to make public the lithotheque as a useful tool for archaeological research, related to the procurement and management of lithic raw materials in Prehistory. Thanks to several research projects that have been carried out, the number of samples is steadily increasing and diversifying, including siliceous rocks collected in Spain, Portugal, France, Jordan and Israel.

  7. Nicotine-magnesium aluminum silicate microparticle surface modified with chitosan for mucosal delivery

    DEFF Research Database (Denmark)

    Kanjanakawinkul, Watchara; Rades, Thomas; Puttipipatkhachorn, Satit


    Magnesium aluminum silicate (MAS), a negatively charged clay, and nicotine (NCT), a basic drug, can interact electrostatically to form microparticles. Chitosan (CS) was used for the surface modification of the microparticles, and a lyophilization method was used to preserve the original particle...... an irregular shape and that their NCT content increased with increasing NCT ratios in the microparticle preparation solution. High molecular weight CS (800 kDa) adsorbed to the microparticle surface and induced a positive surface charge. CS molecules intercalated into the MAS silicate layers and decreased...

  8. Heavily Tm3+-Doped Silicate Fiber for High-Gain Fiber Amplifiers


    Yin-Wen Lee; Han-Wei Chien; Che-Hung Cho; Ju-Zhe Chen; Juin-Shin Chang; Shibin Jiang


    We report on investigation the potential of a 7 wt% (8.35 × 1020 Tm3+/cm3) doped silicate fibers for high-gain fiber amplifiers. Such a high ion concentration significantly reduces the required fiber length of high-power 2 μm fiber laser systems and allows the high-repetition rate operation in 2 μm mode-locked fiber lasers. To evaluate the feasibility of extracting high gain-per-unit-length from this gain medium, we measure several key material properties of the silicate fiber, including the ...

  9. Universality of the high-temperature viscosity limit of silicate liquids

    DEFF Research Database (Denmark)

    Zheng, Qiuju; Mauro, John C.; Ellison, Adam J.


    We investigate the high-temperature limit of liquid viscosity by analyzing measured viscosity curves for 946 silicate liquids and 31 other liquids including metallic, molecular, and ionic systems. Our results show no systematic dependence of the high-temperature viscosity limit on chemical...... composition for the studied liquids. Based on theMauro-Yue-Ellison-Gupta-Allan (MYEGA) model of liquid viscosity, the high-temperature viscosity limit of silicate liquids is 10−2.93 Pa·s. Having established this value, there are only two independent parameters governing the viscosity-temperature relation...

  10. Three-dimensional culture of dental pulp stem cells in direct contact to tricalcium silicate cements. (United States)

    Widbiller, M; Lindner, S R; Buchalla, W; Eidt, A; Hiller, K-A; Schmalz, G; Galler, K M


    Calcium silicate cements are biocompatible dental materials applicable in contact with vital tissue. The novel tricalcium silicate cement Biodentine™ offers properties superior to commonly used mineral trioxide aggregate (MTA). Objective of this study was to evaluate its cytocompatibility and ability to induce differentiation and mineralization in three-dimensional cultures of dental pulp stem cells after direct contact with the material. Test materials included a new tricalcium silicate (Biodentine™, Septodont, Saint-Maur-des-Fossés, France), MTA (ProRoot® MTA, DENSPLY Tulsa Dental Specialities, Johnson City, TN, USA), glass ionomer (Ketac™ Molar Aplicap™, 3M ESPE, Seefeld, Germany), human dentin disks and polystyrene. Magnetic activated cell sorting for to the surface antigen STRO-1 was performed to gain a fraction enriched with mesenchymal stem cells. Samples were allowed to set and dental pulp stem cells in collagen carriers were placed on top. Scanning electron microscopy of tricalcium silicate cement surfaces with and without cells was conducted. Cell viability was measured for 14 days by MTT assay. Alkaline phosphatase activity was evaluated (days 3, 7, and 14) and expression of mineralization-associated genes (COL1A1, ALP, DSPP, and RUNX2) was quantified by real-time quantitative PCR. Nonparametric statistical analysis for cell viability and alkaline phosphatase data was performed to compare different materials as well as time points (Mann-Whitney U test, α = 0.05). Cell viability was highest on tricalcium silicate cement, followed by MTA. Viability on glass ionomer cement and dentin disks was significantly lower. Alkaline phosphatase activity was lower in cells on new tricalcium silicate cement compared to MTA, whereas expression patterns of marker genes were alike. Increased cell viability and similar levels of mineralization-associated gene expression in three-dimensional cell cultures on the novel tricalcium silicate cement and mineral

  11. Mechanical Properties and Durability of Advanced Environmental Barrier Coatings in Calcium-Magnesium-Alumino-Silicate Environments (United States)

    Miladinovich, Daniel S.; Zhu, Dongming


    Environmental barrier coatings are being developed and tested for use with SiC/SiC ceramic matrix composite (CMC) gas turbine engine components. Several oxide and silicate based compositons are being studied for use as top-coat and intermediate layers in a three or more layer environmental barrier coating system. Specifically, the room temperature Vickers-indentation-fracture-toughness testing and high-temperature stability reaction studies with Calcium Magnesium Alumino-Silicate (CMAS or "sand") are being conducted using advanced testing techniques such as high pressure burner rig tests as well as high heat flux laser tests.

  12. Sol-Gel Synthesis, X-Ray Diffraction Studies, and Electric Conductivity of Sodium Europium Silicate

    Directory of Open Access Journals (Sweden)

    Ekaterina V. Borisova


    Full Text Available Sodium europium silicate, NaEu9(SiO46O2, with apatite structure has been obtained and studied using X-ray diffraction and SEM. It has been shown that sodium sublimation does not take place upon synthesis by the sol-gel method. Rietveld refinement has revealed that sodium atoms are ordered and occupy the 4f position. O(4 atoms not related to silicate ions are placed at the centers of Eu(2 triangles. DC and AC electric conductivity and activation energy have been determined for the compound studied.

  13. Rice field test applied by the granular fertilizer made of silicate and oyster sell powder


    森本, 正則; 守本, 信一; 宮本, 信彦; 立木, 陽子; 大黒, 撤平; 樋口, 喜三; 駒井, 功一郎


    [Synopsis] The granular fertilizer made of silicate and oyster sell powder was evaluated the efficacy by application for rice production in the paddy field experiment. The fertilizer was formulated oyster sell powder and silicate using granulator during spray a lignin solution as binder to ingredient powder. Finally, the granular fertilizer contents 1~2% water, 40% CaO, 3% SiO_2 and the particle size is 1~2 mm. The experimental setting was along with conventional rice production in Nara Pref....

  14. A back-arc setting for mafic rocks of the Honeysuckle Beds, southeastern N.S.W.: the use of trace and rare earth element abundances determined by INAA

    Energy Technology Data Exchange (ETDEWEB)

    Dadd, K.A. [University of Technology, Sydney, NSW (Australia)


    Major, trace and rare earth elements abundance in mafic rocks of the Honeysuckle Beds was determined by x-ray fluorescence and neutron activation analysis . A comparison with typical mid-ocean ridge basalt compositions reveals an enrichment in light rare earths elements (Ba, Rb, and Th) and depletion in Nb, Ta and Ti, consistent with modifications of the source by subduction-related fluids. 9 refs., 6 figs.

  15. Low-temperature fabrication of macroporous scaffolds through foaming and hydration of tricalcium silicate paste and their bioactivity

    NARCIS (Netherlands)

    Huan, Z.; Chang, J.; Zhou, J.


    A low-temperature fabrication method for highly porous bioactive scaffolds was developed. The two-step method involved the foaming of tricalcium silicate cement paste and hydration to form calcium silicate hydrate and calcium hydroxide. Scaffolds with a combination of interconnected macro- and

  16. Tracing metal–silicate segregation and late veneer in the Earth and the ureilite parent body with palladium stable isotopes

    DEFF Research Database (Denmark)

    Creech, J. B.; Moynier, F.; Bizzarro, Martin


    Stable isotope studies of highly siderophile elements (HSE) have the potential to yield valuable insights into a range of geological processes. In particular, the strong partitioning of these elements into metal over silicates may lead to stable isotope fractionation during metal–silicate segrega...... with a late-veneer of chondritic material after core formation....

  17. Pre-hydrolysed ethyl silicate as an alternative precursor for SiO{sub 2}-coated carbon nanofibers

    Energy Technology Data Exchange (ETDEWEB)

    Barrena, M.I., E-mail: [Departamento de Ciencia de los Materiales e Ingenieria Metalurgica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Av. Complutense s/n, 28040 Madrid (Spain); Gomez de Salazar, J.M.; Soria, A.; Matesanz, L. [Departamento de Ciencia de los Materiales e Ingenieria Metalurgica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Av. Complutense s/n, 28040 Madrid (Spain)


    This work reported basically aims at understanding the extent of SiO{sub 2}-coated carbon nanofibers using two different sol-gel precursors for the silicate glass. The silicate precursors employed were tetraethoxysilane (TEOS) and pre-hydrolysed ethyl silicate. The first route consisted in an acid hydrolysis and polycondensation of the TEOS and the second one in a polycondensation of the pre-hydrolysed ethyl silicate. The techniques of Fourier Infra Red spectroscopy, thermogravimetric analysis, scanning electron microscopy and X-ray diffraction were used to characterize the materials obtained. Both kinds of SiO{sub 2} precursor can coat the CNF effectively. However, the use of pre-hydrolysed ethyl silicate (faster gelation times and higher surface areas) can be considered a low-cost and facile alternative with respect to the use of TEOS, to obtain industrially silica-coated carbon nanofibers.

  18. Effects of polymer intercalation in calcium silicate hydrates on drug loading capacities and drug release kinetics: an X-ray absorption near edge structure study

    National Research Council Canada - National Science Library

    Guo, Xiaoxuan; Zhu, Ying-Jie; Hu, Yongfeng; Wu, Jin; Yiu, Yun-Mui; Sham, Tsun-Kong


    Different calcium silicate hydrate (CSH)/polymer composites are synthesized by using a controlled precipitation reaction between calcium salt and silicate salt, followed by the addition of various polymer solutions at room temperature...

  19. Impact on the deep biosphere of CO2 geological sequestration in (ultra)mafic rocks and retroactive consequences on its fate (United States)

    Ménez, Bénédicte; Gérard, Emmanuelle; Rommevaux-Jestin, Céline; Dupraz, Sébastien; Guyot, François; Arnar Alfreősson, Helgi; Reynir Gíslason, Sigurőur; Sigurőardóttir, Hólmfríiur


    Due to their reactivity and high potential of carbonation, mafic and ultramafic rocks constitute targets of great interest to safely and permanently sequestrate anthropogenic CO2 and thus, limit the potential major environmental consequences of its increasing atmospheric level. In addition, subsurface (ultra)mafic environments are recognized to harbor diverse and active microbial populations that may be stimulated or decimated following CO2 injection (± impurities) and subsequent acidification. However, the nature and amplitude of the involved biogeochemical pathways are still unknown. To avoid unforeseen consequences at all time scales (e.g. reservoir souring and clogging, bioproduction of H2S and CH4), the impact of CO2 injection on deep biota with unknown ecology, and their retroactive effects on the capacity and long-term stability of CO2 storage sites, have to be determined. We present here combined field and experimental investigations focused on the Icelandic pilot site, implemented in the Hengill area (SW Iceland) at the Hellisheidi geothermal power plant (thanks to the CarbFix program, a consortium between the University of Iceland, Reykjavik Energy, the French CNRS of Toulouse and Columbia University in N.Y., U.S.A. and to the companion French ANR-CO2FIX project). This field scale injection of CO2 charged water is here designed to study the feasibility of storing permanently CO2 in basaltic rocks and to optimize industrial methods. Prior to the injection, the microbiological initial state was characterized through regular sampling at various seasons (i.e., October '08, July '09, February '10). DNA was extracted and amplified from the deep and shallow observatory wells, after filtration of 20 to 30 liters of groundwater collected in the depth interval 400-980 m using a specifically developed sampling protocol aiming at reducing contamination risks. An inventory of living indigenous bacteria and archaea was then done using molecular methods based on the

  20. Mafic microgranular enclaves (MMEs) in amphibole-bearing granites of the Bintang batholith, Main Range granite province: Evidence for a meta-igneous basement in Western Peninsular Malaysia (United States)

    Quek, Long Xiang; Ghani, Azman A.; Chung, Sun-Lin; Li, Shan; Lai, Yu-Ming; Saidin, Mokhtar; Amir Hassan, Meor H.; Muhammad Ali, Muhammad Afiq; Badruldin, Muhammad Hafifi; Abu Bakar, Ahmad Farid


    Mafic microgranular enclaves (MMEs) with varying sizes are a common occurrence in porphyritic amphibole-bearing granite of the Bintang batholith, which is part of the Main Range granite province. The MMEs of the amphibole-bearing granite are significant as they are related to the I-type granitoids within the Main Range granite province. Petrographic observations indicate the MMEs are mantled with coarse mafic crystals on the rim and contain similar minerals to the host (biotite + plagioclase + K-feldspar + pyroxene + amphibole), but in different proportions. Geochemical analyses indicate the MMEs are shoshonitic with mg# comparable to the granite host. Substantial similarities exist between the MMEs and granite with regards to the normalized rare earth element patterns and trace elements variation diagrams. The MMEs and granite are not completely coeval as the MME zircon U-Pb age (224.3 ± 1.2 Ma) is slightly older than its granite host zircon U-Pb age (216.2 ± 1.0 Ma). The age difference is also observed from the unusual 500 m-long Tiak MME and another amphibole-bearing granite sample from the south of the pluton, which yield 221.8 ± 1.1 Ma and 217.4 ± 1.0 Ma respectively. The oldest inherited zircons found in the MME and granite are 2.0 Ga and 1.3 Ga respectively, while the oldest xenocrystic zircons found in the MME and granite are 2.5 Ga and 1.5 Ga respectively. Identical negative εHf(t) values from zircon U-Pb and Lu-Hf analysis for a MME-granite pair indicates the rocks were generated from a similar, ancient source in the basement. Combining the results, we suggest that incongruent melting of an ancient protolith played an important part in the evolution of the MMEs and granite and the MMEs characteristics are best explained as restite. The zircon Hf model age (two-stage) and the I-type peritectic and restitic mineral assemblages in the MMEs further describe the protolith as Early Proterozoic-Late Archean (≈2.5 Ga) meta-igneous rock. This shows the

  1. High-K andesite petrogenesis and crustal evolution: Evidence from mafic and ultramafic xenoliths, Egmont Volcano (Mt. Taranaki) and comparisons with Ruapehu Volcano, North Island, New Zealand (United States)

    Price, Richard C.; Smith, Ian E. M.; Stewart, Robert B.; Gamble, John A.; Gruender, Kerstin; Maas, Roland


    This study uses the geochemistry and petrology of xenoliths to constrain the evolutionary pathways of host magmas at two adjacent andesitic volcanoes in New Zealand's North Island. Egmont (Mt. Taranaki) is located on the west coast of the North Island and Ruapehu lies 140 km to the east at the southern end of the Taupo Volcanic Zone, the principal locus of subduction-related magmatism in New Zealand. Xenoliths are common in the eruptives of both volcanoes but the xenoliths suites are petrographically and geochemically different. Ruapehu xenoliths are predominantly pyroxene-plagioclase granulites derived from Mesozoic meta-greywacke basement and the underlying oceanic crust. The xenolith population of Egmont Volcano is more complex. It includes sedimentary, metamorphic and plutonic rocks from the underlying basement but is dominated by coarse grained, mafic and ultramafic igneous rocks. Gabbroic xenoliths (Group 1) are composed of plagioclase, clinopyroxene and amphibole whereas ultramafic xenoliths are dominated by amphibole (Group 2) or pyroxene (Group 3) or, in very rare cases, olivine (Group 4). In Group 1 xenoliths plagioclase and clinopyroxene and in some cases amphibole show cumulate textures. Amphibole also occurs as intercumulate poikilitic crystals or as blebs or laminae replacing pyroxene. Some Group 2 xenoliths have cumulate textures but near monomineralic amphibole xenoliths are coarse grained with bladed or comb textures. Pyroxene in Group 3 xenoliths has a polygonal granoblastic texture that is commonly overprinted by veining and amphibole replacement. Group 1 and most Group 2 xenoliths have major, trace element and Sr, Nd and Pb isotope compositions indicating affinity with the host volcanic rocks. Geochemical variation can be modelled by assimilation fractional crystallisation (AFC) and fractional crystallisation (FC) of basaltic parents assuming an assimilant with the composition of average crystalline basement and Group 1 xenoliths have

  2. Reactive transport modeling of ferroan dolomitization by seawater interaction with mafic igneous dikes and carbonate host rock at the Latemar platform, Italy (United States)

    Blomme, Katreine; Fowler, Sarah Jane; Bachaud, Pierre


    The Middle Triassic Latemar carbonate platform, northern Italy, has featured prominently in the longstanding debate regarding dolomite petrogenesis [1-4]. Recent studies agree that ferroan and non-ferroan dolomite replaced calcite in limestone during reactive fluid flow at kinetically favorable conditions for the replacement reaction. However, the origin of the dolomitizing fluid is unclear. Seawater may have been an important component, but its Fe concentrations are insufficient to account for ferroan dolomite. New field, petrographic, XRD, and geochemical data document a spatial, temporal, and geochemical link between ferroan replacement dolomite and altered mafic igneous dikes that densely intrude the platform. A critical observation is that ferroan dolomite abundances increase towards the dikes. We hypothesize that seawater interacted with mafic minerals in the dikes, leading to Fe enrichment in the fluid that subsequently participated in dolomitization. This requires that dolomite formation was preceded by dike alteration reactions that liberated Fe and did not consume Mg. Another requirement is that ferroan and non-ferroan dolomite (instead of other Fe- and Mg-bearing minerals) formed during fluid circulation within limestone host rock. We present reactive transport numerical simulations (Coores-Arxim, [5]) that predict equilibrium mineral assemblages and the evolution of fluid dolomitizing potential from dike crystallization, through dike alteration by seawater, to replacement dolomitization in carbonate host rock. The simulations are constrained by observations. A major advantage of the simulations is that stable mineral assemblages are identified based on a forward modeling approach. In addition, the dominant igneous minerals (plagioclase, clinopyroxene olivine and their alteration products) are solid solutions. Most reactive transport simulations of carbonate petrogenesis do not share these benefits (e.g. [6]). Predicted alteration mineral assemblages are

  3. A general route to hollow mesoporous rare-earth silicate nanospheres as a catalyst support. (United States)

    Jin, Renxi; Yang, Yang; Zou, Yongcun; Liu, Xianchun; Xing, Yan


    Hollow mesoporous structures have recently aroused intense research interest owing to their unique structural features. Herein, an effective and precisely controlled synthesis of hollow rare-earth silicate spheres with mesoporous shells is reported for the first time, produced by a simple hydrothermal method, using silica spheres as the silica precursors. The as-prepared hollow rare-earth silicate spheres have large specific surface area, high pore volume, and controllable structure parameters. The results demonstrate that the selection of the chelating reagent plays critical roles in forming the hollow mesoporous structures. In addition, a simple and low-energy-consuming approach to synthesize highly stable and dispersive gold nanoparticle-yttrium silicate (AuNPs/YSiO) hollow nanocomposites has also been developed. The reduction of 4-nitrophenol with AuNPs/YSiO hollow nanocomposites as the catalyst has clearly demonstrated that the hollow rare-earth silicate spheres are good carriers for Au nanoparticles. This strategy can be extended as a general approach to prepare multifunctional yolk-shell structures with diverse compositions and morphologies simply by replacing silica spheres with silica-coated nanocomposites. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. Solid-phase extraction of plant thionins employing aluminum silicate based extraction columns. (United States)

    Hussain, Shah; Güzel, Yüksel; Pezzei, Cornelia; Rainer, Matthias; Huck, Christian W; Bonn, Günther K


    Thionins belong to a family of cysteine-rich, low-molecular-weight (∼5 KDa) biologically active proteins in the plant kingdom. They display a broad cellular toxicity against a wide range of organisms and eukaryotic cell lines. Thionins protect plants against different pathogens, including bacteria and fungi. A highly selective solid-phase extraction method for plant thionins is reported deploying aluminum silicate (3:2 mullite) powder as a sorbent in extraction columns. Mullite was shown to considerably improve selectivity compared to a previously described zirconium silicate embedded poly(styrene-co-divinylbenzene) monolithic polymer. Due to the presence of aluminum(III), mullite offers electrostatic interactions for the selective isolation of cysteine-rich proteins. In comparison to zirconium(IV) silicate, aluminum(III) silicate showed reduced interactions towards proteins which resulted into superior washings of unspecific compounds while still retaining cysteine-rich thionins. In the presented study, European mistletoe, wheat and barley samples were subjected to solid-phase extraction analysis for isolation of viscotoxins, purothionins and hordothionins, respectively. Matrix-assisted laser desorption/ionization time of flight mass spectroscopy was used for determining the selectivity of the sorbent toward thionins. The selectively retained thionins were quantified by colorimetric detection using the bicinchoninic acid assay. For peptide mass-fingerprint analysis tryptic digests of eluates were examined. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Multiple ways of producing intermediate and silicic rocks within Thingmúli and other Icelandic volcanoes

    DEFF Research Database (Denmark)

    Charreteur, Gilles; Tegner, Christian; Haase, Karsten


    Major and trace element compositions of rocks and coexisting phenocrysts of the ThingmA(0)li volcano suggest a revision of the existing models for the formation of intermediate and silicic melts in Iceland. The new data define two compositional tholeiitic trends with a significant gap between them...

  6. Investigation on the effects of combining lime and sodium silicate for ...

    African Journals Online (AJOL)

    Expansive clay is unsuitable subgrade material covering about 40% of the area of Ethiopia. Engineering properties of such problematic soils can be improved by chemical stabilization. This study investigated the effects of combining slightly alkaline liquid sodium silicate with hydrated lime for stabilization of expansive clay.

  7. Analysis of the color alteration and radiopacity promoted by bismuth oxide in calcium silicate cement. (United States)

    Marciano, Marina Angélica; Estrela, Carlos; Mondelli, Rafael Francisco Lia; Ordinola-Zapata, Ronald; Duarte, Marco Antonio Hungaro


    The aim of the study was to determine if the increase in radiopacity provided by bismuth oxide is related to the color alteration of calcium silicate-based cement. Calcium silicate cement (CSC) was mixed with 0%, 15%, 20%, 30% and 50% of bismuth oxide (BO), determined by weight. Mineral trioxide aggregate (MTA) was the control group. The radiopacity test was performed according to ISO 6876/2001. The color was evaluated using the CIE system. The assessments were performed after 24 hours, 7 and 30 days of setting time, using a spectrophotometer to obtain the ΔE, Δa, Δb and ΔL values. The statistical analyses were performed using the Kruskal-Wallis/Dunn and ANOVA/Tukey tests (pbismuth oxide was added showed radiopacity corresponding to the ISO recommendations (>3 mm equivalent of Al). The MTA group was statistically similar to the CSC/30% BO group (p>0.05). In regard to color, the increase of bismuth oxide resulted in a decrease in the ΔE value of the calcium silicate cement. The CSC group presented statistically higher ΔE values than the CSC/50% BO group (pbismuth oxide has no relation to the color alteration of calcium silicate-based cements.

  8. Powder synthesis, processing and characterization of lanthanum silicates for SOFC application

    Energy Technology Data Exchange (ETDEWEB)

    Jothinathan, E.; Vanmeensel, K. [Department of Metallurgy and Materials Engineering, Kasteelpark Arenberg 44, B-3001 Heverlee, Leuven (Belgium); Vleugels, J., E-mail: jozef.vleugels@mtm.kuleuven.b [Department of Metallurgy and Materials Engineering, Kasteelpark Arenberg 44, B-3001 Heverlee, Leuven (Belgium); Van der Biest, O. [Department of Metallurgy and Materials Engineering, Kasteelpark Arenberg 44, B-3001 Heverlee, Leuven (Belgium)


    Recent studies have shown that rare earth silicates exhibit higher oxygen conductivity at lower temperatures (500-800 {sup o}C) compared to traditional yttria-stabilized cubic zirconia. Among the rare earth silicates, doped lanthanum silicates are known to exhibit higher ionic conductivity. The difficulty in sinterability of these powders combined with the fact that the electrolyte material should be sintered onto a porous anode material in a single sintering step to produce SOFC half cells requires very fine starting powders with high sinterability at lower temperatures (1000-1200 {sup o}C). In this paper, we report on the synthesis of lanthanum silicates doped with aluminium or iron using the sol-gel process. Using this fairly simple and quick process, nanometer sized powders with an average grain size below 100 nm have been synthesised, while the intrinsic nanostructure could be maintained in the fully densified electrolyte material after pulsed electric current sintering (PECS) at 1100-1200 {sup o}C.

  9. Anthropogenic Origin of Siliceous Scoria Droplets from Pleistocene and Holocene Archeaological Sites in Northern Syria

    DEFF Research Database (Denmark)

    Thy, Peter; Willcox, George; Barfod, Gry


    to archaeological sites. We therefore conclude that melting of building earth in ancient settlements can occur during !res reaching modest temperatures. There is no evidence to suggest that siliceous scoria droplets result from very high temperature melting of soil and are the result of a cosmic event....

  10. Influence of silicate on enrichment of highly productive microalgae from a mixed culture

    NARCIS (Netherlands)

    Mooij, P.R.; De Jongh, L.D.; Van Loosdrecht, M.C.M.; Kleerebezem, R.


    Microalgae have the potential to supply a biobased society with essential feedstocks like sugar and lipids. Besides being productive, strains used for this purpose should grow fast, be resistant to predators, and have good harvestability properties. Diatoms, a class of siliceous algae, have these

  11. Effect of soaking of seeds in potassium silicate and uniconazole on ...

    African Journals Online (AJOL)



    Jul 13, 2011 ... uniconazole on seed germination and seedling growth of two tomato cultivars. Tomato ( ... containing either 50 or 100 mg L-1 potassium silicate or uniconazole and were placed in an environment controlled chamber (25°C, .... determined with a leaf area meter (LI-3100 area meter, LI-COR. Inc., Lincoln ...

  12. Core Formation on Asteroid 4 Vesta: Iron Rain in a Silicate Magma Ocean (United States)

    Kiefer, Walter S.; Mittlefehldt, David W.


    Geochemical observations of the eucrite and diogenite meteorites, together with observations made by NASA's Dawn spacecraft, suggest that Vesta resembles H chondrites in bulk chemical composition, possibly with about 25% of a CM-chondrite like composition added in. For this model, the core is 15% by mass (or 8 volume %) of the asteroid. The abundances of moderately siderophile elements (Ni, Co, Mo, W, and P) in eucrites require that essentially all of the metallic phase in Vesta segregated to form a core prior to eucrite solidification. Melting in the Fe-Ni-S system begins at a cotectic temperature of 940 deg. C. Only about 40% of the total metal phase, or 3-4 volume % of Vesta, melts prior to the onset of silicate melting. Liquid iron in solid silicate initially forms isolated pockets of melt; connected melt channels, which are necessary if the metal is to segregate from the silicate, are only possible when the metal phase exceeds about 5 volume %. Thus, metal segregation to form a core does not occur prior to the onset of silicate melting.

  13. Synthesis of a novel polyester building block from pentoses by tin-containing silicates

    DEFF Research Database (Denmark)

    Elliot, Samuel Gilbert; Andersen, Christian; Tolborg, Søren


    We report here the direct formation of the new chemical product, trans-2,5-dihydroxy-3-pentenoic acid methyl ester, from pentoses using tin-containing silicates as catalysts. The product is formed under alkali-free conditions in methanol at temperatures in the range 140–180 °C. The highest yields...

  14. The effect of inversion of matrix and inclusions composition in liquation phospho-silicate glasses. (United States)

    Sitarz, M


    Silico-phosphate glasses of XCaPO(4)-SiO(2) and XCaPO(4)-AlPO(4)-SiO(2) (X=Na(+) and/or K(+)) system have been the subject of the presented investigations. Glasses belonging to those systems are characterized by a liquation phenomenon-spherical amorphous inclusions dispersed in an amorphous matrix. Thorough EDX investigations have shown that introduction of aluminum ions into the structure of phospho-silicate glasses results in inversion of matrix and inclusions composition, when XCaPO(4) exceeds 25-35% mol. Such a substantial influence of aluminum ions on phospho-silicate glasses texture as well as matrix and inclusions composition (inversion) must be a result of structural changes. (27)Al MAS NMR research stated that aluminum ions in structures of XCaPO(4)-AlPO(4)-SiO(2) phospho-silicate glasses always acts as a glass-forming ion-i.e. aluminum always occupies fourfold coordinated sites. (23)Na and (31)P MAS NMR research has shown that the inversion of matrix and inclusions composition, brought about by introduction of aluminum ions into the structure of phospho-silicate glasses, is an outcome of a change in phosphorous and alkaline ions coordination. Copyright © 2010 Elsevier B.V. All rights reserved.


    National Research Council Canada - National Science Library

    Svecova, Blanka


    Ion implantation of Au+ with energy of 1.7 MeV and a fluence of 1 x 1016 along with post-implantation annealing were used to synthesize metal nanoparticles in various types of silicate glasses...

  16. Core–shell Au/Ag nanoparticles embedded in silicate sol–gel ...

    Indian Academy of Sciences (India)


    physical rigidity, biodegradation, electrochemical, photochemical, thermal stabilities and optical trans- parency. 14–17 .... charge transfer resistance (Rct) for GC/MTMOS modified electrode due to the silicate matrix film on .... ficient of n = 0⋅99 at a signal to noise ratio of 3. The detection limit was experimentally estimated as.

  17. Characterization of chitosan-magnesium aluminum silicate nanocomposite films for buccal delivery of nicotine

    DEFF Research Database (Denmark)

    Pongjanyakul, Thaned; Khunawattanakul, Wanwisa; Strachan, Clare J


    The objective of this study was to prepare and characterize chitosan-magnesium aluminum silicate (CS-MAS) nanocomposite films as a buccal delivery system for nicotine (NCT). The effects of the CS-MAS ratio on the physicochemical properties, release and permeation, as well as on the mucoadhesive...

  18. Lysozyme-magnesium aluminum silicate microparticles: Molecular interaction, bioactivity and release studies

    DEFF Research Database (Denmark)

    Kanjanakawinkul, Watchara; Medlicott, Natalie J.; Rades, Thomas


    The objectives of this study were to investigate the adsorption behavior of lysozyme (LSZ) onto magnesium aluminum silicate (MAS) at various pHs and to characterize the LSZ–MAS microparticles obtained from the molecular interaction between LSZ and MAS. The results showed that LSZ could be bound...

  19. Effect of magnesium aluminum silicate glass on the thermal shock resistance of BN matrix composite ceramics

    NARCIS (Netherlands)

    Cai, Delong; Jia, Dechang; Yang, Zhihua; Zhu, Qishuai; Ocelik, Vaclav; Vainchtein, Ilia D.; De Hosson, Jeff Th M.; Zhou, Yu

    The effects of magnesium aluminum silicate (MAS) glass on the thermal shock resistance and the oxidation behavior of h-BN matrix composites were systematically investigated at temperature differences from 600 degrees C up to 1400 degrees C. The retained strength rate of the composites rose with the

  20. Distribution of nickel between copper-nickel and alumina saturated iron silicate slags

    Energy Technology Data Exchange (ETDEWEB)

    Reddy, R.G.; Acholonu, C.C.


    The solubility of nickel in slag is determined in this article by equilibrating copper-nickel alloys with alumina-saturated iron silicate slags in an alumina crucible at 1573 K. The results showed that nickel dissolves in slag both as nickel oxide and as nickel metal. The presence of alumina is shown to increase the solubility of nickel in slags.

  1. Water transport in the nano-pore of the calcium silicate phase: reactivity, structure and dynamics. (United States)

    Hou, Dongshuai; Li, Zongjin; Zhao, Tiejun; Zhang, Peng


    Reactive force field molecular dynamics was utilized to simulate the reactivity, structure and dynamics of water molecules confined in calcium-silicate-hydrate (C-S-H) nano-pores of 4.5 nm width. Due to the highly reactive C-S-H surface, hydrolytic reactions occur in the solid-liquid interfacial zone, and partially surface adsorbed water molecules transforming into the Si-OH and Ca-OH groups are strongly embedded in the C-S-H structure. Due to the electronic charge difference, the silicate and calcium hydroxyl groups have binomial distributions of the dipolar moment and water orientation. While Ca-OH contributes to the Ow-downward orientation, the ONB atoms in the silicate chains prefer to accept H-bonds from the surface water molecules. Furthermore, the defective silicate chains and solvated Caw atoms near the surface contribute to the glassy nature of the surface water molecules, with large packing density, pronounced orientation preference, and distorted organization. The stable H-bonds connected with the Ca-OH and Si-OH groups also restrict the mobility of the surface water molecules. The significant reduction of the diffusion coefficient matches well with the experimental results obtained by NMR, QENS and PCFR techniques. Upon increasing the distance from the channel, the structural and dynamic behavior of the water molecules varies and gradually translates into bulk water properties at distances of 10-15 Å from the liquid-solid interface.

  2. In Situ Soft X-ray Spectromicroscopy of Early Tricalcium Silicate Hydration (United States)

    Bae, Sungchul; Kanematsu, Manabu; Hernández-Cruz, Daniel; Moon, Juhyuk; Kilcoyne, David; Monteiro, Paulo J. M.


    The understanding and control of early hydration of tricalcium silicate (C3S) is of great importance to cement science and concrete technology. However, traditional characterization methods are incapable of providing morphological and spectroscopic information about in situ hydration at the nanoscale. Using soft X-ray spectromicroscopy, we report the changes in morphology and molecular structure of C3S at an early stage of hydration. In situ C3S hydration in a wet cell, beginning with induction (~1 h) and acceleration (~4 h) periods of up to ~8 h, was studied and compared with ex situ measurements in the deceleration period after 15 h of curing. Analysis of the near-edge X-ray absorption fine structure showed that the Ca binding energy and energy splitting of C3S changed rapidly in the early age of hydration and exhibited values similar to calcium silicate hydrate (C–S–H). The formation of C–S–H nanoseeds in the C3S solution and the development of a fibrillar C–S–H morphology on the C3S surface were visualized. Following this, silicate polymerization accompanied by C–S–H precipitation produced chemical shifts in the peaks of the main Si K edge and in multiple scattering. However, the silicate polymerization process did not significantly affect the Ca binding energy of C–S–H. PMID:28774096

  3. 40 CFR 721.9514 - Ethyl silicate, reaction products with modified alkoxysilane salt (generic). (United States)


    .... (1) The chemical substance identified generically as Ethyl silicate, reaction products with modified... modified alkoxysilane salt (generic). 721.9514 Section 721.9514 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES...

  4. 78 FR 14540 - Cyromazine, Silica Silicates (Silica Dioxide and Silica Gel), Glufosinate Ammonium, Dioctyl... (United States)


    ... herbicide that acts by inhibiting glutamine synthetase, which leads to poisoning in plants via the...). Silica silicates, silicon dioxide and silica gel, are insecticides and acaracides used in controlling insects at indoor and outdoor sites including a variety of crops. Silicon dioxide is diatomaceous earth, a...

  5. Porosity distribution in root canals filled with gutta percha and calcium silicate cement

    NARCIS (Netherlands)

    Moinzadeh, A.T.; Zerbst, W.; Boutsioukis, C.; Shemesh, H.; Zaslansky, P.


    Objective Gutta percha is commonly used in conjunction with a sealer to produce a fluid-tight seal within the root canal fillings. One of the most commonly used filling methods is lateral compaction of gutta percha coupled with a sealer such as calcium silicate cement. However, this technique may

  6. In Situ Soft X-ray Spectromicroscopy of Early Tricalcium Silicate Hydration

    Directory of Open Access Journals (Sweden)

    Sungchul Bae


    Full Text Available The understanding and control of early hydration of tricalcium silicate (C3S is of great importance to cement science and concrete technology. However, traditional characterization methods are incapable of providing morphological and spectroscopic information about in situ hydration at the nanoscale. Using soft X-ray spectromicroscopy, we report the changes in morphology and molecular structure of C3S at an early stage of hydration. In situ C3S hydration in a wet cell, beginning with induction (~1 h and acceleration (~4 h periods of up to ~8 h, was studied and compared with ex situ measurements in the deceleration period after 15 h of curing. Analysis of the near-edge X-ray absorption fine structure showed that the Ca binding energy and energy splitting of C3S changed rapidly in the early age of hydration and exhibited values similar to calcium silicate hydrate (C–S–H. The formation of C–S–H nanoseeds in the C3S solution and the development of a fibrillar C–S–H morphology on the C3S surface were visualized. Following this, silicate polymerization accompanied by C–S–H precipitation produced chemical shifts in the peaks of the main Si K edge and in multiple scattering. However, the silicate polymerization process did not significantly affect the Ca binding energy of C–S–H.

  7. Attributes of the soil fertilized with sewage sludge and calcium and magnesium silicate

    Directory of Open Access Journals (Sweden)

    Geraldo R. Zuba Junio


    Full Text Available ABSTRACTThis study aimed to evaluate the chemical attributes of an Inceptisol cultivated with castor bean (Ricinus communis L., variety ‘BRS Energia’, fertilized with sewage sludge compost and calcium (Ca and magnesium (Mg silicate. The experiment was conducted at the ICA/UFMG, in a randomized block design, using a 2 x 4 factorial scheme with three replicates, and the treatments consisted of two doses of Ca-Mg silicate (0 and 1 t ha-1 and four doses of sewage sludge compost (0, 23.81, 47.62 and 71.43 t ha-1, on dry basis. Soil organic matter (OM, pH, sum of bases (SB, effective cation exchange capacity (CEC(t, total cation exchange capacity (CEC(T, base saturation (V% and potential acidity (H + Al were evaluated. There were no significant interactions between doses of sewage sludge compost and doses of Ca-Mg silicate on soil attributes, and no effect of silicate fertilization on these attributes. However, fertilization with sewage sludge compost promoted reduction in pH and increase in H + Al, OM and CEC. The dose of 71.43 t ha-1 of sewage sludge compost promoted the best soil chemical conditions.

  8. Productivity and nutritive value of bluestem grass fertilized with calcium and magnesium silicate

    Directory of Open Access Journals (Sweden)

    Cinthya Souza Santana


    Full Text Available This study evaluated the effect of application of calcium and magnesium silicate on the productivity, chemical composition and in situ ruminal degradation of bluestem grass (Andropogon gayanus Kunth, cv. Baeti; Embrapa 23 during the rainy and dry seasons. The design consisted of completely randomized blocks in a 6x2 factorial scheme (six silicate doses and two cutting seasons, arranged in plots subdivided over time. The plots were the calcium and magnesium silicate doses (0, 200, 400, 600, 800 and 1,000 kg/ha and the subplots were the two cutting seasons (rainy and dry period, with five repetitions (blocks. The calcium and magnesium silicate doses exerted no significant effect on green or dry matter production, chemical forage composition or degradability parameters. On the other hand, there was an effect of cutting period on forage production and chemical composition. The highest production of green and dry matter was observed during the rainy period, while acid detergent fiber content was higher during the dry season. The treatments did not exert any significant effect on the parameters of degradability that would alter the nutritive value of bluestem grass.

  9. Core-shell Au/Ag nanoparticles embedded in silicate sol-gel ...

    Indian Academy of Sciences (India)

    The electrocatalytic activity of core-shell Au100-Ag ( = 15, 27, 46, and 60) bimetallic nanoparticles embedded in methyl functionalized silicate MTMOS network towards the reduction of hydrogen peroxide was investigated by using cyclic voltammetry and chronoamperometric techniques. Core-shell Au/Ag bimetallic ...

  10. Composition dependence of luminescence of Eu and Eu/Tb doped silicate glasses for LED applications

    DEFF Research Database (Denmark)

    Zhu, C.F.; Chaussedent, S.; Liu, S.


    The Eu and Eu/Tb doped silicate glasses are good candidates for light emitting diode (LED) applications. But the optical performance of these glasses is sensitive to variations in chemical composition. In this paper we report our recent findings about the effect of addition of minor components su...... curves....

  11. Electronic structure of iron in magnesium silicate glasses at high pressure (United States)

    Gu, Chen; Catalli, Krystle; Grocholski, Brent; Gao, Lili; Alp, Ercan; Chow, Paul; Xiao, Yuming; Cynn, Hyunchae; Evans, William J.; Shim, Sang-Heon


    A recent study attributed the source of an iron partitioning change between silicate melt and minerals at deep mantle conditions to a high-spin to low-spin change in iron, which was found in a Fe-diluted Mg-silicate glass at a similar pressure. We conducted X-ray emission spectroscopy and nuclear forward scattering on iron-rich Mg-silicate glasses at high pressure and 300 K in the diamond-anvil cell: Al-free glass up to 135 GPa and Al-bearing glass up to 93 GPa. In both glasses, the spin moment decreases gradually from 1 bar and does not reach a complete low-spin state even at the peak pressures of this study. The gradual change may be due to the existence of diverse coordination environments for iron in the glasses and continuous structural adjustment of the disordered system with pressure. If the result can be extrapolated to iron in mantle melts, the small, gradual changes in the spin state of iron may not be the dominant factor explaining the reported sudden change in the partitioning behavior of iron between silicate melt and minerals at lower-mantle pressures.

  12. Electrophoretic deposition of calcium silicate-reduced graphene oxide composites on titanium substrate

    DEFF Research Database (Denmark)

    Mehrali, Mehdi; Akhiani, Amir Reza; Talebian, Sepehr


    silicate-reduced graphene oxide (CS-rGO) composites were synthesized, using an in situ hydrothermal method. CS nanowires were uniformly decorated on the rGO, with an appropriate interfacial bonding. The CS-rGO composites behaved like hybrid composites when deposited on a titanium substrate by cathodic...

  13. Preparation and in vivo evaluation of a silicate-based composite bone cement. (United States)

    Ma, Bing; Huan, Zhiguang; Xu, Chen; Ma, Nan; Zhu, Haibo; Zhong, Jipin; Chang, Jiang


    Silicate-based cements have been developed as a class of bioactive and biodegradable bone cements owing to their good in vitro bioactivity and ability to dissolve in a simulated body fluid. Until recently, however, the in vivo evidence of their ability to support bone regeneration is still scarce. In the present study, a pilot in vivo evaluation of a silicate-based composite bone cement (CSC) was carried out in a rabbit femur defect model. The cement was composed of tricalcium silicate, 45S5 bioglass and calcium sulfate, and the self-setting properties of the material were established. The in vivo bone integration and biodegradability of CSC were investigated and compared with those of bioactive glass particulates, and a calcium phosphate cement. The results showed that CSC underwent a relatively slower in vivo degradation as compared with bioactive glass and calcium phosphate cement. Histological observation demonstrated that bone contact area at the interface between the surrounding bone and CSC gradually increased with time proceeding. CSC kept its structural integrity during implantation in vivo because of its acceptable mechanical strength. These results provide evidence of effectiveness in vivo and suggest potential clinical applications of the silicate-based composite bone cements.

  14. Detection of solar wind-produced water in irradiated rims on silicate minerals. (United States)

    Bradley, John P; Ishii, Hope A; Gillis-Davis, Jeffrey J; Ciston, James; Nielsen, Michael H; Bechtel, Hans A; Martin, Michael C


    The solar wind (SW), composed of predominantly ∼1-keV H(+) ions, produces amorphous rims up to ∼150 nm thick on the surfaces of minerals exposed in space. Silicates with amorphous rims are observed on interplanetary dust particles and on lunar and asteroid soil regolith grains. Implanted H(+) may react with oxygen in the minerals to form trace amounts of hydroxyl (-OH) and/or water (H2O). Previous studies have detected hydroxyl in lunar soils, but its chemical state, physical location in the soils, and source(s) are debated. If -OH or H2O is generated in rims on silicate grains, there are important implications for the origins of water in the solar system and other astrophysical environments. By exploiting the high spatial resolution of transmission electron microscopy and valence electron energy-loss spectroscopy, we detect water sealed in vesicles within amorphous rims produced by SW irradiation of silicate mineral grains on the exterior surfaces of interplanetary dust particles. Our findings establish that water is a byproduct of SW space weathering. We conclude, on the basis of the pervasiveness of the SW and silicate materials, that the production of radiolytic SW water on airless bodies is a ubiquitous process throughout the solar system.

  15. Formation and Detection of Clay Network Structure in Poly(propylene) /Layered Silicate Nanocomposites

    NARCIS (Netherlands)

    Abranyi, Agnes; Szazdi, Laszlo; Pukanszky Jr., Bela; Vancso, Gyula J.; Pukanszky, B.; Pukanszky, Bela


    The study of the structure and the rheological properties of poly(propylene) (PP)/montmorillonite (MMT)/maleinated PP (MAPP) composites strongly suggests that a silicate network may form under certain conditions. Network formation could not be proven unambiguously with the usual techniques, i.e.,

  16. Energetics of silicate melts from thermal diffusion studies. Annual progress report

    Energy Technology Data Exchange (ETDEWEB)

    Walker, D.


    Efforts are reported in the following areas: laboratory equipment (multianvils for high P/T work, pressure media, SERC/DL sychrotron), liquid-state thermal diffusion (silicate liquids, O isotopic fractionation, volatiles, tektites, polymetallic sulfide liquids, carbonate liquids, aqueous sulfate solutions), and liquid-state isothermal diffusion (self-diffusion, basalt-rhyolite interdiffusion, selective contamination, chemical diffusion).

  17. Flow perfusion culture of human mesenchymal stem cells on silicate-substituted tricalcium phosphate scaffolds

    DEFF Research Database (Denmark)

    Jensen, Lea Bjerre; Bünger, Cody; Kassem, Moustapha


    Autologous bone grafts are currently the gold standard for treatment of large bone defects, but their availability is limited due to donor site morbidity. Different substitutes have been suggested to replace these grafts, and this study presents a bone tissue engineered alternative using silicate...

  18. Effect of ethyl silicate on salt crystallization resistance of Maastricht limestone

    NARCIS (Netherlands)

    Lubelli, B.A.; Hees, R.P.J.; Nijland, T.G.; Bolhuis, J.


    consolidant treatments aim to re-establish the cohesion in declayed materials showing decqay patterns as sanding or powdering. Ethyl silicate (TEOS) is the most used type of consolidant for inorganic porous materials in the last 30 years. This product which works through precipitation of silica gel

  19. Determination of Thermal Conductivity of Silicate Matrix for Applications in Effective Media Theory (United States)

    Fiala, Lukáš; Jerman, Miloš; Reiterman, Pavel; Černý, Robert


    Silicate materials have an irreplaceable role in the construction industry. They are mainly represented by cement-based- or lime-based materials, such as concrete, cement mortar, or lime plaster, and consist of three phases: the solid matrix and air and water present in the pores. Therefore, their effective thermal conductivity depends on thermal conductivities of the involved phases. Due to the time-consuming experimental determination of the effective thermal conductivity, its calculation by means of homogenization techniques presents a reasonable alternative. In the homogenization theory, both volumetric content and particular property of each phase need to be identified. For porous materials the most problematic part is to accurately identify thermal conductivity of the solid matrix. Due to the complex composition of silicate materials, the thermal conductivity of the matrix can be determined only approximately, based on the knowledge of thermal conductivities of its major compounds. In this paper, the thermal conductivity of silicate matrix is determined using the measurement of a sufficiently large set of experimental data. Cement pastes with different open porosities are prepared, dried, and their effective thermal conductivity is determined using a transient heat-pulse method. The thermal conductivity of the matrix is calculated by means of extrapolation of the effective thermal conductivity versus porosity functions to zero porosity. Its practical applicability is demonstrated by calculating the effective thermal conductivity of a three-phase silicate material and comparing it with experimental data.

  20. Composite nanoparticles: A new way to siliceous materials and a model of biosilica synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Annenkov, Vadim V., E-mail: [Limnological Institute, Siberian Branch of the Russian Academy of Sciences, Irkutsk 664033 (Russian Federation); Pal' shin, Viktor A.; Verkhozina, Olga N. [Limnological Institute, Siberian Branch of the Russian Academy of Sciences, Irkutsk 664033 (Russian Federation); Larina, Lyudmila I. [A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk 664033 (Russian Federation); Danilovtseva, Elena N. [Limnological Institute, Siberian Branch of the Russian Academy of Sciences, Irkutsk 664033 (Russian Federation)


    A new polyampholyte based on poly (acrylic acid) which bears pendant polyamine oligomeric chains (average number of the nitrogen atoms is 11.2) is obtained. This polymer is a model of silaffins – proteins playing important role in formation of siliceous structures in diatom algae and sponges. The polymer catalyses condensation of silicic acid. The obtained solutions contain oligosilicates coordinated with the polymer chains. The action of 50,000 g gravity on this solution results in concentrating-induced condensation of the pre-condensed siliceous oligomers. The obtained solid silica contains 4% admixture of the organic polymer which is close to the silica from diatom frustules. These results confirm the hypothesis about formation of biosilica under the action of desiccation agent, e.g. aquaporins. The formation of solid substances during centrifugation of solutions containing soluble oligomers is a new promising approach to inorganic and composite materials which allows to work in aqueous medium and to reuse the organic polymer. - Highlights: • A polyampholyte with pendant polyamine chains is obtained. • The polymer catalyses condensation of silicic acid giving stable solutions. • Gravity-induced (50,000 g) formation of solid silica was observed in these solutions. • The obtained silica is close to biosilica from diatom frustules. • A new approach to inorganic and composite materials is proposed.