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Sample records for alkali feldspar plagioclase

  1. Anisotropy of magnetic susceptibility in alkali feldspar and plagioclase

    NASA Astrophysics Data System (ADS)

    Biedermann, Andrea R.; Pettke, Thomas; Angel, Ross J.; Hirt, Ann M.

    2016-04-01

    Feldspars are the most abundant rock-forming minerals in the Earth's crust, but their magnetic properties have not been rigorously studied. This work focuses on the intrinsic magnetic anisotropy of 31 feldspar samples with various chemical compositions. Because feldspar is often twinned or shows exsolution textures, measurements were performed on twinned and exsolved samples as well as single crystals. The anisotropy is controlled by the diamagnetic susceptibility and displays a consistent orientation of principal susceptibility axes; the most negative or minimum susceptibility is parallel to [010], and the maximum (least negative) is close to the crystallographic [001] axis. However, the magnetic anisotropy is weak when compared to other rock-forming minerals, 1.53 × 10-9 m3 kg-1 at maximum. Therefore, lower abundance minerals, such as augite, hornblende or biotite, often dominate the bulk paramagnetic anisotropy of a rock. Ferromagnetic anisotropy is not significant in most samples. In the few samples that do show ferromagnetic anisotropy, the principal susceptibility directions of the ferromagnetic subfabric do not display a systematic orientation with respect to the feldspar lattice. These results suggest that palaeointensity estimates of the geomagnetic field made on single crystals of feldspar will not be affected by a systematic orientation of the ferromagnetic inclusions within the feldspar lattice.

  2. Elasticity of plagioclase feldspars

    NASA Astrophysics Data System (ADS)

    Brown, J. Michael; Angel, Ross J.; Ross, Nancy L.

    2016-02-01

    Elastic properties are reported for eight plagioclase feldspars that span compositions from albite (NaSi3AlO8) to anorthite (CaSi2Al2O8). Surface acoustic wave velocities measured using Impulsive Stimulated Light Scattering and compliance sums from high-pressure X-ray compression studies accurately determine all 21 components of the elasticity tensor for these triclinic minerals. The overall pattern of elasticity and the changes in individual elastic components with composition can be rationalized on the basis of the evolution of crystal structures and chemistry across this solid-solution join. All plagioclase feldspars have high elastic anisotropy; a* (the direction perpendicular to the b and c axes) is the softest direction by a factor of 3 in albite. From albite to anorthite the stiffness of this direction undergoes the greatest change, increasing twofold. Small discontinuities in the elastic components, inferred to occur between the three plagioclase phases with distinct symmetry (C1>¯, I1>¯, and P1>¯), appear consistent with the nature of the underlying conformation of the framework-linked tetrahedra and the associated structural changes. Measured body wave velocities of plagioclase-rich rocks, reported over the last five decades, are consistent with calculated Hill-averaged velocities using the current moduli. This confirms long-standing speculation that previously reported elastic moduli for plagioclase feldspars are systematically in error. The current results provide greater assurance that the seismic structure of the middle and lower crusts can be accurately estimated on the basis of specified mineral modes, chemistry, and fabric.

  3. Europium anomaly in plagioclase feldspar: experimental results and semiquantitative model.

    PubMed

    Weill, D F; Drake, M J

    1973-06-01

    The partition of europium between plagioclase feldspar and magmatic liquid is considered in terms of the distribution coefficients for divalent and trivalent europium. A model equation is derived giving the europium anomaly in plagioclase as a function of temperature and oxygen fugacity. The model explains europium anomalies in plagioclase synthesized under controlled laboratory conditions as well as the variations of the anomaly observed in natural terrestrial and extraterrestrial igneous rocks.

  4. Europium anomaly in plagioclase feldspar - Experimental results and semiquantitative model.

    NASA Technical Reports Server (NTRS)

    Weill, D. F.; Drake, M. J.

    1973-01-01

    The partition of europium between plagioclase feldspar and magmatic liquid is considered in terms of the distribution coefficients for divalent and trivalent europium. A model equation is derived giving the europium anomaly in plagioclase as a function of temperature and oxygen fugacity. The model explains europium anomalies in plagioclase synthesized under controlled laboratory conditions as well as the variations of the anomaly observed in natural terrestrial and extraterrestrial igneous rocks.

  5. Europium anomaly in plagioclase feldspar: experimental results and semiquantitative model.

    PubMed

    Weill, D F; Drake, M J

    1973-06-01

    The partition of europium between plagioclase feldspar and magmatic liquid is considered in terms of the distribution coefficients for divalent and trivalent europium. A model equation is derived giving the europium anomaly in plagioclase as a function of temperature and oxygen fugacity. The model explains europium anomalies in plagioclase synthesized under controlled laboratory conditions as well as the variations of the anomaly observed in natural terrestrial and extraterrestrial igneous rocks. PMID:17806582

  6. Cathodoluminescence Characterization of Maskelynite and Alkali Feldspar in Shergottite (Dhofar 019)

    SciTech Connect

    Kayama, M.; Nakazato, T.; Nishido, H.; Ninagawa, K.; Gucsik, A.

    2009-08-17

    Dhofar 019 is classified as an olivine-bearing basaltic shergottite and consists of subhedral grains of pyroxene, olivine, feldspar mostly converted to maskelynite and minor alkali feldspar. The CL spectrum of its maskelynite exhibits an emission band at around 380 nm. Similar UV-blue emission has been observed in the plagioclase experimentally shocked at 30 and 40 GPa, but not in terrestrial plagioclase. This UV-blue emission is a notable characteristic of maskelynite. CL spectrum of alkali feldspar in Dhofar 019 has an emission bands at around 420 nm with no red emission. Terrestrial alkali feldspar actually consists of blue and red emission at 420 and 710 nm assigned to Al-O{sup -}-Al and Fe{sup 3+} centers, respectively. Maskelynite shows weak and broad Raman spectral peaks at around 500 and 580 cm{sup -1}. The Raman spectrum of alkali feldspar has a weak peak at 520 cm{sup -1}, whereas terrestrial counterpart shows the emission bands at 280, 400, 470, 520 and 1120 cm{sup -1}. Shock pressure on this meteorite transformed plagioclase and alkali feldspar into maskelynite and almost glass phase, respectively. It eliminates their luminescence centers, responsible for disappearance of yellow and/or red emission in CL of maskelynite and alkali feldspar. The absence of the red emission band in alkali feldspar can also be due to the lack of Fe{sup 3+} in the feldspar as it was reported for some lunar feldspars.

  7. Modeling H, Na, and K diffusion in plagioclase feldspar by relating point defect parameters to bulk properties

    NASA Astrophysics Data System (ADS)

    Zhang, Baohua; Shan, Shuangming; Wu, Xiaoping

    2016-02-01

    Hydrogen and alkali ion diffusion in plagioclase feldspars is important to study the evolution of the crust and the kinetics of exsolution and ion-exchange reactions in feldspars. Using the available PVT equation of state of feldspars, we show that the diffusivities of H and alkali in plagioclase feldspars as a function of temperature can be successfully reproduced in terms of the bulk elastic and expansivity data through a thermodynamic model that interconnects point defect parameters with bulk properties. Our calculated diffusion coefficients of H, Na, and K well agree with experimental ones when uncertainties are considered. Additional point defect parameters such as activation enthalpy, activation entropy, and activation volume are also predicted. Furthermore, the electrical conductivity of feldspars inferred from our predicted diffusivities of H, Na, and K through the Nernst-Einstein equation is compared with previous experimental data.

  8. Thermal infrared spectroscopy and modeling of experimentally shocked plagioclase feldspars

    USGS Publications Warehouse

    Johnson, J. R.; Horz, F.; Staid, M.I.

    2003-01-01

    Thermal infrared emission and reflectance spectra (250-1400 cm-1; ???7???40 ??m) of experimentally shocked albite- and anorthite-rich rocks (17-56 GPa) demonstrate that plagioclase feldspars exhibit characteristic degradations in spectral features with increasing pressure. New measurements of albite (Ab98) presented here display major spectral absorptions between 1000-1250 cm-1 (8-10 ??m) (due to Si-O antisymmetric stretch motions of the silica tetrahedra) and weaker absorptions between 350-700 cm-1 (14-29 ??m) (due to Si-O-Si octahedral bending vibrations). Many of these features persist to higher pressures compared to similar features in measurements of shocked anorthite, consistent with previous thermal infrared absorption studies of shocked feldspars. A transparency feature at 855 cm-1 (11.7 ??m) observed in powdered albite spectra also degrades with increasing pressure, similar to the 830 cm-1 (12.0 ??m) transparency feature in spectra of powders of shocked anorthite. Linear deconvolution models demonstrate that combinations of common mineral and glass spectra can replicate the spectra of shocked anorthite relatively well until shock pressures of 20-25 GPa, above which model errors increase substantially, coincident with the onset of diaplectic glass formation. Albite deconvolutions exhibit higher errors overall but do not change significantly with pressure, likely because certain clay minerals selected by the model exhibit absorption features similar to those in highly shocked albite. The implication for deconvolution of thermal infrared spectra of planetary surfaces (or laboratory spectra of samples) is that the use of highly shocked anorthite spectra in end-member libraries could be helpful in identifying highly shocked calcic plagioclase feldspars.

  9. Visible/near-infrared spectra of experimentally shocked plagioclase feldspars

    USGS Publications Warehouse

    Johnson, J. R.; Horz, F.

    2003-01-01

    High shock pressures cause structural changes in plagioclase feldspars such as mechanical fracturing and disaggregation of the crystal lattice at submicron scales, the formation of diaplectic glass (maskelynite), and genuine melting. Past studies of visible/ near-infrared spectra of shocked feldspars demonstrated few spectral variations with pressure except for a decrease in the depth of the absorption feature near 1250-1300 nm and an overall decrease in reflectance. New visible/near-infrared spectra (400-2500 nm) of experimentally shocked (17-56 GPa) albite- and anorthite-rich rock powders demonstrate similar trends, including the loss of minor hydrated mineral bands near 1410, 1930, 2250, and 2350 nm. However, the most interesting new observations are increases in reflectance at intermediate pressures, followed by subsequent decreases in reflectance at higher pressures. The amount of internal scattering and overall sample reflectance is controlled by the relative proportions of micro-fractures, submicron grains, diaplectic glass, and melts formed during shock metamorphism. We interpret the observed reflectance increases at intermediate pressures to result from progressively larger proportions of submicron feldspar grains and diaplectic glass. The ensuing decreases in reflectance occur after diaplectic glass formation is complete and the proportion of genuine melt inclusions increases. The pressure regimes over which these reflectance variations occur differ between albite and anorthite, consistent with thermal infrared spectra of these samples and previous studies of shocked feldspars. These types of spectral variations associated with different peak shock pressures should be considered during interpretation and modeling of visible/near-infrared remotely sensed spectra of planetary and asteroidal surfaces.

  10. Raman Study of Shock Effects in Plagioclase Feldspar from the Mistastin Lake Impact Structure, Canada

    NASA Astrophysics Data System (ADS)

    Xie, T. X.; Shieh, S. R. S.; Osinski, G. R. O.

    2016-08-01

    This study mainly uses Raman spectroscopy with a 514 nm laser to study anorthosite from Mistastin Lake Impact Crater, Canada, which mainly contains plagioclase with composition of An 28–55, to better understand shock processes in plagioclase feldspar.

  11. Raman Study of Shock Effects in Plagioclase Feldspar from the Mistastin Lake Impact Structure, Canada

    NASA Astrophysics Data System (ADS)

    Xie, T. X.; Shieh, S. R. S.; Osinski, G. R. O.

    2016-08-01

    This study mainly uses Raman spectroscopy with a 514 nm laser to study anorthosite from Mistastin Lake Impact Crater, Canada, which mainly contains plagioclase with composition of An 28-55, to better understand shock processes in plagioclase feldspar.

  12. Electron microprobe study of lunar and planetary zoned plagioclase feldspars: An analytical and experimental study of zoning in plagioclase

    NASA Technical Reports Server (NTRS)

    Smith, R. K.; Lofgren, G. E.

    1982-01-01

    Natural and experimentally grown zoned plagioclase feldspars were examined by electron microprobe. The analyses revealed discontinuous, sector, and oscillary chemical zoning superimposed on continuous normal or reverse zoning trends. Postulated mechanisms for the origin of zoning are based on either physical changes external to the magma (P, T, H2O saturation) or kinetic changes internal to the magma (diffusion, supersaturation, growth rate). Comparison of microprobe data on natural zoned plagioclase with zoned plagioclase grown in controlled experiments show that it may be possible to distinguish zonal development resulting from physio-chemical changes to the bulk magma from local kinetic control on the growth of individual crystals.

  13. Elastic properties of alkali-feldspars

    NASA Astrophysics Data System (ADS)

    Waeselmann, N.; Brown, J.; Angel, R. J.; Ross, N.; Kaminsky, W.

    2013-12-01

    New measurements of single crystal elastic moduli for a suite of the alkali feldspars are reported. In order to interpret Earth's seismic structure, knowledge of the elastic properties of constituent minerals is essential. The elasticity of feldspar minerals, despite being the most abundant phase in Earth's crust (estimated to be more than 60%), were previously poorly characterized. All prior seismic and petrologic studies have utilized 50-year-old results, of questionable quality, based on 1-bar measurements on pseudo-single crystals. Alkali-feldspars present a large experimental challenge associated with their structural complexity. In the K-end member (KAlSi3O8) the symmetry is governed by Al/Si ordering, in the Na-end member (NaAlSi3O8) the symmetry is governed by whether or not there is a displacive collapse of the framework independent of the Al/Si ordering. K-feldspars exhibit monoclinic (C2/m) symmetry (necessitating determination of 13 elastic moduli) if disordered and triclinic (C-1) symmetry (21 elastic moduli) if ordered. Exsolution of Na-rich and K-rich phases is ubiquitous in natural samples, making it difficult to find suitable single phase and untwinned samples for study. The small single domain samples selected for this study were previously characterized by x-ray diffraction and microprobe analysis to ensure adequate sample quality. Surface wave velocities were measured on oriented surfaces of natural and synthetic single crystals using impulsively stimulated light scattering. A surface corrugation with a spacing of about 2 microns was impulsively created by the overlap of 100 ps infrared light pulses. The time evolution of the stimulated standing elastic waves was detected by measuring the intensity of diffraction from the surface corrugation of a variably delayed probe pulse. This method allows accurate (better than 0.2%) determination of velocities on samples smaller than 100 microns. The combination of measured surface wave velocities and

  14. Shock effects in plagioclase feldspar from the Mistastin Lake impact structure, Canada

    NASA Astrophysics Data System (ADS)

    Pickersgill, Annemarie E.; Osinski, Gordon R.; Flemming, Roberta L.

    2015-09-01

    Shock metamorphism, caused by hypervelocity impact, is a poorly understood process in feldspar due to the complexity of the crystal structure, the relative ease of weathering, and chemical variations, making optical studies of shocked feldspars challenging. Understanding shock metamorphism in feldspars, and plagioclase in particular, is vital for understanding the history of Earth's moon, Mars, and many other planetary bodies. We present here a comprehensive study of shock effects in andesine and labradorite from the Mistastin Lake impact structure, Labrador, Canada. Samples from a range of different settings were studied, from in situ central uplift materials to clasts from various breccias and impact melt rocks. Evidence of shock metamorphism includes undulose extinction, offset twins, kinked twins, alternate twin deformation, and partial to complete transformation to diaplectic plagioclase glass. In some cases, isotropization of alternating twin lamellae was observed. Planar deformation features (PDFs) are notably absent in the plagioclase, even when present in neighboring quartz grains. It is notable that various microlites, twin planes, and compositionally different lamellae could easily be mistaken for PDFs and so care must be taken. A pseudomorphous zeolite phase (levyne-Ca) was identified as a replacement mineral of diaplectic feldspar glass in some samples, which could, in some instances, also be potentially mistaken for PDFs. We suggest that the lack of PDFs in plagioclase could be due to a combination of structural controls relating to the crystal structure of different feldspars and/or the presence of existing planes of weakness in the form of twin and cleavage planes.

  15. Infrared reflectance spectra (2. 2-15. mu. m) of plagioclase feldspars

    SciTech Connect

    Nash, D.B. ); Salisbury, J.W. )

    1991-06-01

    Laboratory results show that (1) the Christiansen frequency (CF) feature in mid-infrared reflectance spectra of powders can be used to accurately distinguish plagioclase composition, and (2) the wavelength position of the CF is not affected by vitrification of the plagioclase. Although the CF position does not distinguish glass from crystalline forms of plagioclase, other features (combination-tone, overtone, restrahlen bands) in the mid-IR spectra of plagioclase can be used for that purpose. These results have important implications for application of thermal emission spectroscopy to mapping the surface composition of regolith-covered planetary bodies like the Moon, Mars, and asteroids.

  16. Partitioning of Eu and Sr between coexisting plagioclase and K-feldspar.

    NASA Technical Reports Server (NTRS)

    Nagasawa, H.

    1971-01-01

    Minerals were separated by an EM approach and with the aid of liquids of great density. An analysis of K, Rb, Ca, Sr, Ha, and rare earth elements was conducted by means of a mass spectrometer isotope dilution technique. The behavior of the divalent europium ions during the partition process was found to be very similar to that of divalent strontium ions, taking into consideration data of the partition coefficients between coexisting feldspars in acidic rocks.

  17. Cryptic microtextures and geological histories of K-rich alkali feldspars revealed by charge contrast imaging

    NASA Astrophysics Data System (ADS)

    Flude, Stephanie; Lee, Martin R.; Sherlock, Sarah C.; Kelley, Simon P.

    2012-06-01

    Charge contrast imaging in the scanning electron microscope can provide new insights into the scale and composition of alkali feldspar microtextures, and such information helps considerably with the interpretation of their geological histories and results of argon isotope thermochronological analyses. The effectiveness of this technique has been illustrated using potassium-rich alkali feldspars from the Dartmoor granite (UK). These feldspars contain strain-controlled lamellar crypto- and microperthites that are cross-cut by strain-free deuteric microperthites. The constituent albite- and orthoclase-rich phases of both microperthite generations can be readily distinguished by atomic number contrast imaging. The charge contrast results additionally show that sub-micrometre-sized albite `platelets' are commonplace between coarser exsolution lamellae and occur together to make cryptoperthites. Furthermore, charge contrast imaging reveals that the orthoclase-rich feldspar is an intergrowth of two phases, one that is featureless with uniform contrast and another that occurs as cross-cutting veins and grains with the {110} adularia habit. Transmission electron microscopy shows that the featureless feldspar is tweed orthoclase, whereas the veins and euhedral grains are composed of irregular microcline that has formed from orthoclase by `unzipping' during deuteric or hydrothermal alteration. The charge contrast imaging results are especially important in demonstrating that deuteric perthites are far more abundant in alkali feldspars than would be concluded from investigations using conventional microscopy techniques. The unexpected presence of such a high volume of replacement products has significant implications for understanding the origins and geological histories of crustal rocks and the use of alkali feldspars in geo- and thermochronology. Whilst the precise properties of feldspars that generate contrast remain unclear, the similarity between charge contrast images

  18. Thermodynamic assessment of hydrothermal alkali feldspar-mica-aluminosilicate equilibria

    USGS Publications Warehouse

    Sverjensky, D.A.; Hemley, J.J.; d'Angelo, W. M.

    1991-01-01

    The thermodynamic properties of minerals retrieved from consideration of solid-solid and dehydration equilibria with calorimetric reference values, and those of aqueous species derived from studies of electrolytes, are not consistent with experimentally measured high-temperature solubilities in the systems K2O- and Na2O-Al2O3-SiO2-H2O-HCl (e.g., K-fs - Ms - Qtz - K+ - H+). This introduces major inaccuracies into the computation of ionic activity ratios and the acidities of diagenetic, metamorphic, and magmatic hydrothermal fluids buffered by alkali silicate-bearing assemblages. We report a thermodynamic analysis of revised solubility equilibria in these systems that integrates the thermodynamic properties of minerals obtained from phase equilibria studies (Berman, 1988) with the properties of aqueous species calculated from a calibrated equation of state (Shock and Helgeson, 1988). This was achieved in two separate steps. First, new values of the free energies and enthalpies of formation at 25??C and 1 bar for the alkali silicates muscovite and albite were retrieved from the experimental solubility equilibria at 300??C and Psat. Because the latter have stoichiometric reaction coefficients different from those for solid-solid and dehydration equilibria, our procedure preserves exactly the relative thermodynamic properties of the alkali-bearing silicates (Berman, 1988). Only simple arithmetic adjustments of -1,600 and -1,626 (??500) cal/mol to all the K- and Na-bearing silicates, respectively, in Berman (1988) are required. In all cases, the revised values are within ??0.2% of calorimetric values. Similar adjustments were derived for the properties of minerals from Helgeson et al. (1978). Second, new values of the dissociation constant of HCl were retrieved from the solubility equilibria at temperatures and pressures from 300-600??C and 0.5-2.0 kbars using a simple model for aqueous speciation. The results agree well with the conductance-derived dissociation

  19. Shock melting of K-feldspar and interlacing with cataclastically deformed plagioclase in granitic rocks at Toqqusap Nunaa, southern West Greenland: Implications for the genesis of the Maniitsoq structure

    NASA Astrophysics Data System (ADS)

    Keulen, Nynke; Garde, Adam A.; Jørgart, Tommy

    2015-11-01

    Folded sheets of Mesoarchaean, leucocratic plagioclase-K-feldspar-mesoperthite-bearing granitic rocks in the Toqqusap Nunaa area of the Maniitsoq structure, West Greenland, are characterised by their very fine grain sizes and microstructures without normal igneous or planar/linear tectonic fabrics. Quartz forms equidimensional and branching, ductilely deformed aggregates and bifurcating panels with protrusions, constrictions and chains of ball-shaped grains with healed, radiating intergranular fractures. Plagioclase (An10-20) was cataclastically deformed and comminuted, whereas K-feldspar and mesoperthite are devoid of cataclastic microstructures. K-feldspar forms dispersed, highly irregular grains with numerous cusps and saddles, indicating almost ubiquitous direct (shock) melting of this mineral. It is commonly located along former fractures in plagioclase, resulting in an 'interlaced' feldspar microstructure with contact shapes indicating subsequent melting of plagioclase directly adjacent to K-feldspar. Mesoperthite forms separate, rounded, and irregular grains with protrusions and cusped margins indicating crystallisation from melts. Some mesoperthite grains are texturally and compositionally heterogeneous and contain internal lenses of K-feldspar and/or plagioclase. Other mesoperthite grains comprise coarsened, 'unzipped' areas, presumably due to localised, fluid-controlled dissolution-reprecipitation processes. The ternary feldspar precursor of the mesoperthite is interpreted as having crystallised from variably effectively mixed K-feldspar shock melts and plagioclase contact melts. Direct melting of K-feldspar, but no whole-rock melting, requires shock metamorphism with a short-lived temperature excursion to above the melting temperature of K-feldspar (~ 1300 °C). The presence of three different feldspar species and absence of chemical zonation, magmatic mantling, or metamorphic coronas furthermore hinders interpretations solely by means of endogenic

  20. Ultraviolet-blue ionic luminescence of alkali feldspars from bulk and interfaces

    NASA Astrophysics Data System (ADS)

    Garcia-Guinea, J.; Townsend, P. D.; Sanchez-Muñoz, L.; Rojo, J. M.

    Laboratory driven ionic thermal exchange of alkali feldspars from K to Na produces samples which are strongly luminescent in the ultraviolet region near 320nm. The sites providing this luminescence are suggested as being correlated with the motion of Na atoms along interface-interphases of the material (i.e. with Na-O bond fracture). The thermoluminescence peaks show multi-order kinetics. Thermal preheatings of low albite sensitize the feldspar lattice with respect to thermoluminescence generated by exposure to UV irradiation and heating produces a strong blue luminescence spread over the range 350nm to 500nm band in feldspars. The upper temperature for thermoluminescence in feldspars is 300°C, which is also the point where ionic conductivity of albite (010) begins, but the 300°C region is also the starting point of a large second glow peak in adularia. Whilst it seems appropriate to link the Na motion to the 350-500nm emission, it is unclear whether these changes are the result of the large anisotropic thermal vibration of Na atoms or the massive Na jumps that occur when the lattice reaches 300°C. A speculative model is considered in which the UV TL emissions of natural minerals are linked to different interface-interphases (grain boundaries, exsolution limits, twinning planes, antiphase domains). Increased interface coherency energies are related to the kinetic order and the spectral position of luminescence emission peaks.

  1. Crystallization kinetics of alkali feldspars in cooling and decompression-induced crystallization experiments in trachytic melt

    NASA Astrophysics Data System (ADS)

    Arzilli, Fabio; Carroll, Michael R.

    2013-10-01

    Cooling and decompression experiments have been carried out on trachytic melts in order to investigate crystallization kinetics of alkali feldspar, the effect of the degree of undercooling ( ΔT = T liquidus - T experimental) and time on nucleation and crystal growth process. This experimental work gives us new data about crystallization kinetics of trachytic melts, and it that will be useful to better understand the natural system of Campi Flegrei volcanoes. Experiments have been conducted using cold seal pressure vessel apparatus, at pressure between 30 and 200 MPa, temperature between 750 and 855 °C, time between 7,200 and 57,600 s and redox condition close to the NNO +0.8 buffer. These conditions are ideal to reproducing pre- and syn-eruptive conditions of the Campi Flegrei volcanoes, where the "conditions" pertain to the complete range of pressures, temperatures and time at which the experiments were performed. Alkali feldspar is the main phase present in this trachyte, and its abundance can strongly vary with small changes in pressure, temperature and water content in the melt, implying appreciable variations in the textures and in the crystallization kinetics. The obtained results show that crystallization kinetics are strictly related to ΔT, time, final pressure, superheating (- ΔT) and water content in the melt. ΔT is the driving force of the crystallization, and it has a strong influence on nucleation and growth processes. In fact, the growth process dominates crystallization at small ΔT, whereas the nucleation dominates crystallization at large ΔT. Time also is an important variable during crystallization process, because long experiment durations involve more nucleation events of alkali feldspar than short experiment durations. This is an important aspect to understand magma evolution in the magma chamber and in the conduit, which in turn has strong effects on magma rheology.

  2. Towards a more practical two-feldspar geothermometer

    NASA Astrophysics Data System (ADS)

    Brown, William L.; Parsons, Ian

    1981-07-01

    The thermodynamic basis of several recent attempts to formulate a simple two-feldspar geothermometer is discussed, together with a review of earlier empirical geothermometers and ones based on experimental studies in the ternary feldspar system. It is shown that double-binary thermometers which involve the combination of regular solution mixing models for the binary alkali feldspar system with ideal mixing in plagioclases do not give a satisfactory representation of two-feldspar relations, especially for albite-rich compositions where a critical point exists. Thermometers based on mixing parameters for ordered alkali feldspar frameworks are even more unjustified both because low-plagioclases are certainly non-ideal, and because of uncertainty in knowing the degree of Al-Si order in the alkali feldspar when exchange equilibrium was achieved. A ‘thermodynamic’ thermometer requires knowledge of ternary activities which are at present unknown. Experimental determinations of relationships in the ternary feldspar system are reviewed and the correct general form of the thermometer constructed using mainly the experimental data of Seck (1971a) and Smith and Parsons (1974). Chemographic tests for equilibrium between feldspar pairs are suggested and petrographie features discussed. In an appendix new values are given of Margules parameters calculated for binary disordered alkali feldspars from recent solvus data up to 15 kbars, and their physico-chemical basis examined. We suggest that accurate representations of the mixing properties of disordered alkali feldspars using Margules parameters are at present premature.

  3. 3D distribution and evolution of porosity during albitization and patch perthitization of alkali feldspars

    NASA Astrophysics Data System (ADS)

    Norberg, N.; Neusser, G.; Wirth, R.; Harlov, D. E.

    2010-12-01

    Fluid-mediated replacement of minerals and rocks often results in the formation of an extensive porosity. This reaction-induced porosity is generally assumed to be pervasive enabling the constant progress of the alteration process and fluid infiltration of initially impermeable rocks (e.g. Putnis, 2009 Rev Min Geochem, 70, 87). This hypothesis was tested utilizing state-of-the-art micro- to nano-analytical techniques including FIB in combination with SEM and TEM. For this study two different alkali feldspar replacement reactions common in natural rocks were reproduced experimentally; (i) albitization of K-rich alkali-feldspar (Or85-95) and (ii) patch perthitization of intermediate (exsolved) alkali feldspars (Ab60Or40). 3D analysis of the pore distribution was done by a combination of alternate removal of 100 nm slices using FIB followed by SE imaging of the dissected surface. Series of 100-200 SE images were obtained from 20 × 8 × 20 µm3 sample blocks and translated into a 3-dimensional model using Fiji software package (resolution ~0.03 × 0.03 × 0.1 µm3). Analyses of the experimentally albitized and patch-perthitized alkali feldspar demonstrate that in both cases single-crystalline starting materials are replaced by highly porous, polycrystalline replacement products. In the case of albitization the replacement rim consists of two generations of polycrystalline intergrowths of slightly tilted albite sub-grains visible in TEM. These are a fine-grained, highly porous and a coarse-grained, almost non-porous albite that seems to progressively replace the former. The total reaction-induced porosity clearly exceeds the difference in the molar volume of the reaction of ~ -7.5%. Pores are mostly elongated forming several micron long channels. However, despite the abundance of porosity within the albitized areas, neither 3D analysis nor TEM could detect any significant interconnection between these channels. The same holds true in the case of patch perthitization

  4. Na/K-interdiffusion in alkali feldspar: new data on diffusion anisotropy and composition dependence

    NASA Astrophysics Data System (ADS)

    Schaeffer, Anne-Kathrin; Petrishcheva, Elena; Habler, Gerlinde; Abart, Rainer; Rhede, Dieter

    2013-04-01

    Exchange experiments between gem-quality alkali feldspar with an initial XOr of 0.85 or 0.72 and Na/K-salt melts have been conducted at temperatures between 800° and 1000° C. The crystals were prepared as crystallographically oriented plates, the polished surfaces corresponding to the (010) or (001) plane of the feldspar. The composition of the melts was varied systematically to induce a controlled shift of the feldspar towards more Na-rich or K-rich compositions (XOr 0.5 to 1). A molar excess of cations by a factor of 40 in the melt ensured constant concentration boundary conditions for cation exchange. Different geometries of diffusion profiles can be observed depending on the direction of the composition shift. For a shift towards more K-rich compositions the diffusion profile exhibits two plateaus corresponding to an exchanged rim in equilibrium with the melt and a completely unexchanged core, respectively. Between these plateaus an exchange front develops with an inflection point that progresses into the crystal with t1-2. The width of this diffusion front varies greatly with the extent of chemical shift and crystallographic direction. The narrowest profiles are always found in the direction normal to (010), i.e. b, marking the slowest direction of interdiffusion. A shift towards more Na-rich composition leads to the development of a crack system due to the composition strain associated with the substitution of the larger K+ion with the smaller Na+ion. The exchange front developing in this case lacks the inflection point observed for shifts towards more K-rich compositions. The observed geometry of the diffusion fronts can be explained by a composition dependence of the interdiffusion coefficient. We used the Boltzmann transformation to calculate the interdiffusion coefficient in dependence of composition from our data in a range between XOr 0.5 and 1 for profiles normal to both (010) and (001) and for different temperatures. As indicated by the different

  5. Pristine moon rocks - An alkali anorthosite with coarse augite exsolution from plagioclase, a magnesian harzburgite, and other oddities

    NASA Technical Reports Server (NTRS)

    Warren, P. H.; Jerde, E. A.; Kallemeyn, G. W.

    1990-01-01

    Results are presented on the analyses of 18 samples of pristine rocks obtained from the primarily mare Apollo 12 site and from the primarily highland Apollo 14 site, as well as samples from the nonmare Apollo 15 site. It was found that, while two of anorthosites from Apollo 12 were similar in composition to most other anorthosites from the west-central near region, the texture of an alkali anorthosite featured a long and narrow crystal of augite surrounded by a single crystal of plagioclase, clearly suggesting that the augite formed by exsolution out of the plagioclase. Another Apollo 12 rocklet was an unusual magnesian harzburite, with subequal amounts of enstatite and olivine, traces of Cr-Fe spinel, and FeNi metal, but no plagioclase; the bulk composition was found to be remarkably Ir-rich (53 percent) for a pristine rock, and the texture was also unusual. Apollo 14 samples included several uncommonly Al-rich and REE-poor impact melt breccias.

  6. Ionic conductivity in gem-quality single-crystal alkali feldspar from the Eifel: temperature, orientation and composition dependence

    NASA Astrophysics Data System (ADS)

    El Maanaoui, Hamid; Wilangowski, Fabian; Maheshwari, Aditya; Wiemhöfer, Hans-Dieter; Abart, Rainer; Stolwijk, Nicolaas A.

    2016-05-01

    We measured the ion conductivity of single-crystal alkali feldspar originating from two different locations in the Eifel/Germany, named Volkesfeld and Rockeskyller sanidine and having potassium site fractions C_K of 0.83 and 0.71, respectively. The dc conductivities resulting from electrochemical impedance spectroscopy over the temperature range of 300-900°C show a weak composition dependence but pronounced differences between the b-direction [perp (010)] and c^{*}-direction [perp (001)] of the monoclinic feldspar structure. Conductivity activation energies obtained from the observed linear Arrhenius plots are close to 1.2 eV in all cases, which is closely similar to the activation energies of the ^{22}Na tracer diffusivity in the same crystals. Taking into account literature data on K tracer diffusion and diffusion correlation effects, the present results point to a predominance of the interstitialcy mechanism over the vacancy mechanism in mass and charge transport on the alkali sublattice in potassium-rich alkali feldspar.

  7. Time-temperature evolution of microtextures and contained fluids in a plutonic alkali feldspar during heating

    NASA Astrophysics Data System (ADS)

    Parsons, Ian; Fitz Gerald, John D.; Lee, James K. W.; Ivanic, Tim; Golla-Schindler, Ute

    2010-08-01

    Microtextural changes brought about by heating alkali feldspar crystals from the Shap granite, northern England, at atmospheric pressure, have been studied using transmission and scanning electron microscopy. A typical unheated phenocryst from Shap is composed of about 70 vol% of tweed orthoclase with strain-controlled coherent or semicoherent micro- and crypto-perthitic albite lamellae, with maximum lamellar thicknesses <1 μm. Semicoherent lamellae are encircled by nanotunnel loops in two orientations and cut by pull-apart cracks. The average bulk composition of this microtexture is Ab27.6Or71.8An0.6. The remaining 30 vol% is deuterically coarsened, microporous patch and vein perthite composed of incoherent subgrains of oligoclase, albite and irregular microcline. The largest subgrains are ~3 μm in diameter. Heating times in the laboratory were 12 to 6,792 h and T from 300°C into the melting interval at 1,100°C. Most samples were annealed at constant T but two were heated to simulate an 40Ar/39Ar step-heating schedule. Homogenisation of strain-controlled lamellae by Na↔K inter-diffusion was rapid, so that in all run products at >700°C, and after >48 h at 700°C, all such regions were essentially compositionally homogeneous, as indicated by X-ray analyses at fine scale in the transmission electron microscope. Changes in lamellar thickness with time at different T point to an activation energy of ~350 kJmol-1. A lamella which homogenised after 6,800 h at 600°C, therefore, would have required only 0.6 s to do so in the melting interval at 1,100°C. Subgrains in patch perthite homogenised more slowly than coherent lamellae and chemical gradients in patches persisted for >5,000 h at 700°C. Homogenisation T is in agreement with experimentally determined solvi for coherent ordered intergrowths, when a 50-100°C increase in T for An1 is applied. Homogenisation of lamellae appears to proceed in an unexpected manner: two smooth interfaces, microstructurally sharp

  8. Experimental Na/K exchange between alkali feldspar and an NaCl-KCl salt melt: chemically induced fracturing and element partitioning

    NASA Astrophysics Data System (ADS)

    Neusser, G.; Abart, R.; Fischer, F. D.; Harlov, D.; Norberg, N.

    2012-08-01

    The exchange of Na+ and K+ between alkali feldspar and a NaCl-KCl salt melt has been investigated experimentally. Run conditions were at ambient pressure and 850 °C as well as 1,000 °C. Cation exchange occurred by interdiffusion of Na+ and K+ on the feldspar sub-lattice, while the Si-Al framework remained unaffected. Due to the compositional dependence of the lattice parameters compositional heterogeneities resulting from Na+/K+ interdiffusion induced coherency stress and associated fracturing. Depending on the sense of chemical shift, different crack patterns developed. For the geometrically most regular case that developed when potassic alkali feldspar was shifted toward more sodium-rich compositions, a prominent set of cracks corresponding to tension cracks opened perpendicular to the direction of maximum tensile stress and did not follow any of the feldspar cleavage planes. The critical stress needed to initiate fracturing in a general direction of the feldspar lattice was estimated at ≤0.35 GPa. Fracturing provided fast pathways for penetration of salt melt or vapor into grain interiors enhancing overall cation exchange. The Na/K partitioning between feldspar and the salt melt attained equilibrium values in the exchanged portions of the grains allowing for extraction of the alkali feldspar mixing properties.

  9. Can cathodoluminescence of feldspar be used as provenance indicator?

    NASA Astrophysics Data System (ADS)

    Scholonek, Christiane; Augustsson, Carita

    2016-05-01

    We have studied feldspar from crystalline rocks for its textural and spectral cathodoluminescence (CL) characteristics with the aim to reveal their provenance potential. We analyzed ca. 60 rock samples of plutonic, volcanic, metamorphic, and pegmatitic origin from different continents and of 16 Ma to 2 Ga age for their feldspar CL textures and ca. 1200 feldspar crystals from these rocks for their CL color spectra. Among the analyzed rocks, igneous feldspar is most commonly zoned, whereby oscillatory zoning can be confirmed to be typical for volcanic plagioclase. The volcanic plagioclase also less commonly contains twin lamellae that are visible in CL light than crystals from other rock types. Alkali feldspar, particularly from igneous and pegmatitic rocks, was noted to be most affected by alteration features, visible as dark spots, lines and irregular areas. The size of all textural features of up to ca. 150 μm, in combination with possible alteration in both the source area and the sedimentary system, makes the CL textures of feldspar possible to use for qualitative provenance research only. We observed alkali feldspar mostly to luminesce in a bluish color and sometimes in red, and plagioclase in green to yellow. The corresponding CL spectra are dominated by three apparent intensity peaks at 440-520 nm (mainly blue), 540-620 nm (mainly green) and 680-740 nm (red to infrared). A dominance of the peak in the green wavelength interval over the blue one for plagioclase makes CL particularly useful for the differentiation of plagioclase from alkali feldspar. An apparent peak position in red to infrared at < 710 nm for plagioclase mainly is present in mafic rocks. Present-day coastal sand from Peru containing feldspar with the red to infrared peak position mainly exceeding 725 nm for northern Peruvian sand and a larger variety for sand from southern Peru illustrates a discriminative effect of different source areas. We conclude that the provenance application

  10. Not all feldspars are equal: a survey of ice nucleating properties across the feldspar group of minerals

    NASA Astrophysics Data System (ADS)

    Harrison, Alexander D.; Whale, Thomas F.; Carpenter, Michael A.; Holden, Mark A.; Neve, Lesley; O'Sullivan, Daniel; Vergara Temprado, Jesus; Murray, Benjamin J.

    2016-09-01

    Mineral dust particles from wind-blown soils are known to act as effective ice nucleating particles in the atmosphere and are thought to play an important role in the glaciation of mixed phase clouds. Recent work suggests that feldspars are the most efficient nucleators of the minerals commonly present in atmospheric mineral dust. However, the feldspar group of minerals is complex, encompassing a range of chemical compositions and crystal structures. To further investigate the ice-nucleating properties of the feldspar group we measured the ice nucleation activities of 15 characterized feldspar samples. We show that alkali feldspars, in particular the potassium feldspars, generally nucleate ice more efficiently than feldspars in the plagioclase series which contain significant amounts of calcium. We also find that there is variability in ice nucleating ability within these groups. While five out of six potassium-rich feldspars have a similar ice nucleating ability, one potassium rich feldspar sample and one sodium-rich feldspar sample were significantly more active. The hyper-active Na-feldspar was found to lose activity with time suspended in water with a decrease in mean freezing temperature of about 16 °C over 16 months; the mean freezing temperature of the hyper-active K-feldspar decreased by 2 °C over 16 months, whereas the "standard" K-feldspar did not change activity within the uncertainty of the experiment. These results, in combination with a review of the available literature data, are consistent with the previous findings that potassium feldspars are important components of arid or fertile soil dusts for ice nucleation. However, we also show that there is the possibility that some alkali feldspars may have enhanced ice nucleating abilities, which could have implications for prediction of ice nucleating particle concentrations in the atmosphere.

  11. Cathodoluminescence of quartz and feldspar in provenance research

    NASA Astrophysics Data System (ADS)

    Augustsson, Carita; Reker, Annalena; Scholonek, Christiane

    2013-04-01

    Quartz often dominates in siliciclastic sandstone and feldspar mostly is present. Despite this, the use of quartz and feldspar in provenance research is limited. Feldspar is less stable than both quartz and many other minerals that are used to trace sources rocks, such as zircon and rutile. Nevertheless, particularly quartz and zircon may survive many sedimentary recycling phases. Therefore they do not necessarily give information about first-cycle sources. Hence, the wide occurrence of feldspar and quartz in sedimentary rocks is an excellent condition to trace both first-cycle and multi-cycle sediment sources. The cathodoluminescence (CL) technique enables the consideration of both minerals. We analysed ca. 1000 quartz crystals and ca. 1200 feldspar crystals in ca. 60 samples each for their CL colour spectra to investigate their provenance potential. They originate from different plutonic, volcanic, metamorphic, and pegmatitic rocks. The CL colours of quartz vary from red over violet to different shades of blue and brown. They are due to lattice defects and trace element contents that are caused by different crystallisation conditions and later lattice reorganisation. The corresponding CL spectra are dominated by two apparent intensity peaks at 470-490 nm (blue) and at 600-640 nm (red). Distinctive relative intensity differences in these two peaks occur for (1) quartz of volcanic origin, (2) felsic plutonic and high-temperature metamorphic quartz, and (3) low-temperature metamorphic quartz. Feldspar often luminesces in different shades of blue, green, yellow, and red due to substitution elements. Alkali feldspar usually has a bright blue colour and plagioclase often is green. The corresponding CL spectra are dominated by three apparent intensity peaks at 420-500 nm (blue), 540-570 nm (green) and 690-760 nm (red to infrared). The CL is particularly useful for the distinction of plagioclase from alkali feldspar. Here, a dominance of the peak in green over the peak

  12. Coupled alkali feldspar dissolution and secondary mineral precipitation in batch systems: 4. Numerical modeling of kinetic reaction paths

    NASA Astrophysics Data System (ADS)

    Zhu, Chen; Lu, Peng; Zheng, Zuoping; Ganor, Jiwchar

    2010-07-01

    This paper explores how dissolution and precipitation reactions are coupled in batch reactor experimental systems at elevated temperatures. This is the fourth paper in our series of "Coupled Alkali Feldspar Dissolution and Secondary Mineral Precipitation in Batch Systems". In our third paper, we demonstrated via speciation-solubility modeling that partial equilibrium between secondary minerals and aqueous solutions was not attained in feldspar hydrolysis batch reactors at 90-300 °C and that a strong coupling between dissolution and precipitation reactions follows as a consequence of the slower precipitation of secondary minerals ( Zhu and Lu, 2009). Here, we develop this concept further by using numerical reaction path models to elucidate how the dissolution and precipitation reactions are coupled. Modeling results show that a quasi-steady state was reached. At the quasi-steady state, dissolution reactions proceeded at rates that are orders of magnitude slower than the rates measured at far from equilibrium. The quasi-steady state is determined by the relative rate constants, and strongly influenced by the function of Gibbs free energy of reaction ( ΔG) in the rate laws. To explore the potential effects of fluid flow rates on the coupling of reactions, we extrapolate a batch system ( Ganor et al., 2007) to open systems and simulated one-dimensional reactive mass transport for oligoclase dissolution and kaolinite precipitation in homogeneous porous media. Different steady states were achieved at different locations along the one-dimensional domain. The time-space distribution and saturation indices (SI) at the steady states were a function of flow rates for a given kinetic model. Regardless of the differences in SI, the ratio between oligoclase dissolution rates and kaolinite precipitation rates remained 1.626, as in the batch system case ( Ganor et al., 2007). Therefore, our simulation results demonstrated coupling among dissolution, precipitation, and flow rates

  13. Principles of Thermal Expansion in Feldspars

    NASA Astrophysics Data System (ADS)

    Hovis, Guy; Medford, Aaron; Conlon, Maricate; Tether, Allison; Romanoski, Anthony

    2010-05-01

    Following the recent thermal expansion work of Hovis et al. (1) on AlSi3 feldspars, we have investigated the thermal expansion of plagioclase, Ba-K, and Ca-K feldspar crystalline solutions. X-ray powder diffraction data were collected between room temperature and 925 °C on six natural plagioclase specimens ranging in composition from anorthite to oligoclase, the K-exchanged equivalents of these plagioclase specimens, and five synthetic Ba-K feldspars with compositions ranging from 25 to 99 mol % BaAl2Si2O8. The resulting thermal expansion coefficients (α) for volume have been combined with earlier results for end-member Na- and K-feldspars (2,3). Unlike AlSi3 feldspars, Al2Si2 feldspars, including anorthite and celsian from the present study plus Sr- and Pb-feldspar from other workers (4,5), show essentially constant and very limited thermal expansion, regardless of divalent cation size. In the context of structures where the Lowenstein rule (6) requires Al and Si to alternate among tetrahedra, the proximity of bridging Al-O-Si oxygen ions to divalent neighbors (ranging from 0 to 2) produces short Ca-O (or Ba-O) bonds (7,8) that apparently are the result of local charge-balance requirements (9). Gibbs et al. (10) suggest that short bonds such as these have a partially covalent character. This in turn stiffens the structure. Thus, for feldspar series with coupled substitution the change away from a purely divalent M-site occupant gives the substituting (less strongly bonded) monovalent cations increasingly greater influence on thermal expansion. Overall, then, thermal expansion in the feldspar system is well represented on a plot of α against room-temperature volume, where one sees a quadrilateral bounded by data for (A) AlSi3 feldspars whose expansion behavior is controlled largely by the size of the monovalent alkali-site occupant, (B) Al2Si2 feldspars whose expansion is uniformly limited by partially-covalent bonds between divalent M-site occupants and

  14. A detailed study of ice nucleation by feldspar minerals

    NASA Astrophysics Data System (ADS)

    Whale, T. F.; Murray, B. J.; Wilson, T. W.; Carpenter, M. A.; Harrison, A.; Holden, M. A.; Vergara Temprado, J.; Morris, J.; O'Sullivan, D.

    2015-12-01

    Immersion mode heterogeneous ice nucleation plays a crucial role in controlling the composition of mixed phase clouds, which contain both supercooled liquid water and ice particles. The amount of ice in mixed phase clouds can affect cloud particle size, lifetime and extent and so affects radiative properties and precipitation. Feldspar minerals are probably the most important minerals for ice nucleation in mixed phase clouds because they nucleate ice more efficiently than other components of atmospheric mineral dust (Atkinson et al. 2013). The feldspar class of minerals is complex, containing numerous chemical compositions, several crystal polymorphs and wide variations in microscopic structure. Here we present the results of a study into ice nucleation by a wide range of different feldspars. We found that, in general, alkali feldspars nucleate ice more efficiently than plagioclase feldspars. However, we also found that particular alkali feldspars nucleate ice relatively inefficiently, suggesting that chemical composition is not the only important factor that dictates the ice nucleation efficiency of feldspar minerals. Ice nucleation by feldspar is described well by the singular model and is probably site specific in nature. The alkali feldspars that do not nucleate ice efficiently possess relatively homogenous structure on the micrometre scale suggesting that the important sites for nucleation are related to surface topography. Ice nucleation active site densities for the majority of tested alkali feldspars are similar to those found by Atkinson et al (2013), meaning that the validity of global aerosol modelling conducted in that study is not affected. Additionally, we have found that ice nucleation by feldspars is strongly influenced, both positively and negatively, by the solute content of droplets. Most other nucleants we have tested are unaffected by solutes. This provides insight into the mechanism of ice nucleation by feldspars and could be of importance

  15. Trace-element partitioning at conditions far from equilibrium: Ba and Cs distributions between alkali feldspar and undercooled hydrous granitic liquid at 200 MPa

    NASA Astrophysics Data System (ADS)

    Morgan, George; London, David

    2002-12-01

    This study examines the effects of increasing supersaturation, attained by single-step liquidus undercooling (ΔT), on the partitioning of barium and cesium between potassic alkali feldspar (Afs) and hydrous granitic liquid at 200 MPa. The investigation is motivated by trace-element distribution patterns in granitic pegmatites which cannot be simulated by fractionation models using "equilibrium" partition coefficients, and thus its purpose is to assess if, how, and why partition coefficients for compatible and incompatible trace elements may vary when crystal growth commences far from the crystal-melt equilibrium boundary. Barium expands the liquidus stability field of potassic feldspar to higher temperatures, such that liquidi for the Ba-rich ( 0.5 wt% BaO) compositions used are 100 °C higher than for Ba-absent analogues. At low degrees of undercooling (ΔT 50 °C), values of DBaAfs/m. ( 10-20) fall within the range of previous investigations, as do values of DCsAfs/m. (<=0.10) from experiments at all temperatures. Progressively greater undercooling is manifested in the run products by increasingly skeletal to cuneiform crystal morphologies, increased compositional zonation of Afs, and the development of compositional boundary layers in glass. Whereas the partitioning behavior of Cs (incompatible) is not measurably affected, strong undercooling apparently causes the partitioning of Ba (highly compatible) to deviate from equilibrium behavior. Feldspars produced by strong undercooling (ΔT>=100 °C) are heterogeneous, such that DBaAfs/m. versus K/K+Na varies linearly between the average value at 850 °C and the equilibrium value appropriate to the temperature of growth. Hence, high supersaturation accompanying undercooling produces feldspar compositions by isothermal growth which record a vestige of the liquid line of descent (i.e., an ontogeny within zoned crystals which approximately tracks the feldspar liquidus from high temperature to the final low temperature

  16. Observation of micron to centimetre scale argon in alkali feldspars: implications for 40Ar/39Ar thermochronology

    NASA Astrophysics Data System (ADS)

    Kelley, S. P.; Flude, S.

    2012-04-01

    New data from gem quality K-feldspar from Itrongay, Madagascar indicates that such crystals behave as a single diffusion domain for Ar diffusion. A study of such a grain allows us to measure natural Ar diffusion from micron to centimetre scales in gem quality feldspars. UV-laserprobe 40Ar/39Ar ages from single gem quality grains indicate that the natural crystal surface acted as the main diffusion domain boundary. UV-Laser ablation 40Ar/39Ar dating of 1 cm whole crystal of gem quality K-feldspar was undertaken at a range of length scales. Micron scale UV laser depth profiling was used to determine Ar diffusion adjacent to the natural crystal surface (presumed to have formed as the pegmatite crystalised). UV laser spot dating was used to measure the age variations on a length scales of 10s of microns to mm and even cm. The high potassium content and age of the Itrongay sample make it possible to measure natural argon diffusion at high precision and high spatial resolution, to address some of the issues surrounding Ar diffusion, at a scale that can be imaged in the laboratory. The analysis reveals the presence of age gradients in the Itrongay feldspar spanning more than 50Ma - between 420 and 470 Ma. As previous work on Itrongay feldspar has tended to be carried out on mm-sized fragments without knowledge of the original crystal boundaries, the variation in radiometric ages in the published literature is likely due to these internal age variations. These gradients are interpreted as diffusion profiles caused by the diffusion loss of 40Ar from the crystal and we have modeled the likely differences between slow cooling/storage at elevated temperature, episodic loss, or different diffusion mechanisms. The age gradients appear to be in agreement with previous thermochronology in the area.

  17. Alkali feldspar dissolution and secondary mineral precipitation in batch systems: 3. Saturation states of product minerals and reaction paths

    NASA Astrophysics Data System (ADS)

    Zhu, Chen; Lu, Peng

    2009-06-01

    In order to evaluate the complex interplay between dissolution and precipitation reaction kinetics, we examined the hypothesis of partial equilibria between secondary mineral products and aqueous solutions in feldspar-water systems. Speciation and solubility geochemical modeling was used to compute the saturation indices (SI) for product minerals in batch feldspar dissolution experiments at elevated temperatures and pressures and to trace the reaction paths on activity-activity diagrams. The modeling results demonstrated: (1) the experimental aqueous solutions were supersaturated with respect to product minerals for almost the entire duration of the experiments; (2) the aqueous solution chemistry did not evolve along the phase boundaries but crossed the phase boundaries at oblique angles; and (3) the earlier precipitated product minerals did not dissolve but continued to precipitate even after the solution chemistry had evolved into the stability fields of minerals lower in the paragenesis sequence. These three lines of evidence signify that product mineral precipitation is a slow kinetic process and partial equilibria between aqueous solution and product minerals were not held. In contrast, the experimental evidences are consistent with the hypothesis of strong coupling of mineral dissolution/precipitation kinetics [e.g., Zhu C., Blum A. E. and Veblen D. R. (2004a) Feldspar dissolution rates and clay precipitation in the Navajo aquifer at Black Mesa, Arizona, USA. In Water-Rock Interaction (eds. R. B. Wanty and R. R. I. Seal). A.A. Balkema, Saratoga Springs, New York. pp. 895-899]. In all batch experiments examined, the time of congruent feldspar dissolution was short and supersaturation with respect to the product minerals was reached within a short period of time. The experimental system progressed from a dissolution driven regime to a precipitation limited regime in a short order. The results of this study suggest a complex feedback between dissolution and

  18. Origin of hydrous alkali feldspar-silica intergrowth in spherulites from intra-plate A2-type rhyolites at the Jabal Shama, Saudi Arabia

    NASA Astrophysics Data System (ADS)

    Surour, Adel A.; El-Nisr, Said A.; Bakhsh, Rami A.

    2016-03-01

    Miocene rhyolites (19.2 ± 0.9 Ma) at the Jabal Shama in western Saudi Arabia represent an example of rift-related silicic volcanism that took place during the formation of the Red Sea. They mostly consist of tuffaceous varieties with distinct flow banding, and pea-sized spherulites, obsidian and perlitized rhyolite tuffs. Although they have the geochemical signature of A2-type rhyolites, these silicic rocks are not typically alkaline but alkali-calcic to calc-alkaline. They developed in a within-plate regime and possibly derived from a recycled mafic subducted slab in depleted sub-continental mantle beneath the western Arabian plate. The Jabal Shama rhyolites are younger in age than their Miocene counterparts in Yemen and Ethiopia. The Jabal Shama spherulites consist of hydrous alkali feldspar-silica radial intergrowths with an occasional brown glass nucleus. Carbonate- and glass-free spherulites give up to 4.45 wt% L.O.I. The hydrous nature of these silicates and the absence of magnetite in the spherulites is a strong indication of oxidizing conditions. The spherulites contain hydrous feldspars with up to ∼6 wt% H2O, and they develop by diffusion and devitrification of glass in the rhyolite tuff at ∼800 °C. Owing to higher undercooling due to supersaturation, the radial hydrous phases within spherulites might grow faster and led to coagulation. The polygonal contacts between spherulites and the ∼120° dihedral angle suggest solid-state modification and recrystallization as the process of devitrification proceeds as low as ∼300 °C. The sum of FeO + MgO is positively correlated with total alkalies along with magnetite oxidation in the matrix to Fe-oxyhydroxides, and to the incorporation of OH- into silicates within the spehrulites themselves. Structural H2O in glass of the Jabal Shama perlite (obsidian) is considerable (∼9-12 wt%) with 3.72-5.6 wt% L.O.I. of the whole-rock. The presence of deleterious silica impurities would lower the ore grade due to

  19. The Thermal Expansion Of Feldspars

    NASA Astrophysics Data System (ADS)

    Hovis, G. L.; Medford, A.; Conlon, M.

    2009-12-01

    Hovis and others (1) investigated the thermal expansion of natural and synthetic AlSi3 feldspars and demonstrated that the coefficient of thermal expansion (α) decreases significantly, and linearly, with increasing room-temperature volume (VRT). In all such feldspars, therefore, chemical expansion limits thermal expansion. The scope of this work now has been broadened to include plagioclase and Ba-K feldspar crystalline solutions. X-ray powder diffraction data have been collected between room temperature and 925 °C on six plagioclase specimens ranging in composition from anorthite to oligoclase. When combined with thermal expansion data for albite (2,3,4) a steep linear trend of α as a function of VRT emerges, reflecting how small changes in composition dramatically affect expansion behavior. The thermal expansion data for five synthetic Ba-K feldspars ranging in composition from 20 to 100 mole percent celsian, combined with data for pure K-feldspar (3,4), show α-VRT relationships similar in nature to the plagioclase series, but with a slope and intercept different from the latter. Taken as a group all Al2Si2 feldspars, including anorthite and celsian from the present study along with Sr- (5) and Pb-feldspar (6) from other workers, show very limited thermal expansion that, unlike AlSi3 feldspars, has little dependence on the divalent-ion (or M-) site occupant. This apparently is due to the necessitated alternation of Al and Si in the tetrahedral sites of these minerals (7), which in turn locks the tetrahedral framework and makes the M-site occupant nearly irrelevant to expansion behavior. Indeed, in feldspar series with coupled chemical substitution it is the change away from a 1:1 Al:Si ratio that gives feldspars greater freedom to expand. Overall, the relationships among α, chemical composition, and room-temperature volume provide useful predictive tools for estimating feldspar thermal expansion and give insight into the controls of expansion behavior in

  20. Calorimetric investigation of the excess entropy of mixing in analbite-sanidine solid solutions: lack of evidence for Na,K short- range order and implications for two-feldspar thermometry.

    USGS Publications Warehouse

    Haselton, H.T.; Hovis, G.L.; Hemingway, B.S.; Robie, R.A.

    1983-01-01

    Heat capacities (5-380 K) have been measured by adiabatic calorimetry for five highly disordered alkali feldspars (Ab99Or1, Ab85Or15, Ab55Or45, Ab25Or75 and Ab1Or99). The thermodynamic and mineralogical implications of the results are discussed. The new data are also combined with recent data for plagioclases in order to derive a revised expression for the two-feldspar thermometer. T calculated from the revised expression tend to be higher than previous calculations.-J.A.Z.

  1. Systematic variations of argon diffusion in feldspars and implications for thermochronometry

    SciTech Connect

    Cassata, William S.; Renne, Paul R.

    2013-03-07

    Coupled information about the time-dependent production and temperature-dependent diffusion of radiogenic argon in feldspars can be used to constrain the thermal evolution attending a host of Earth and planetary processes. To better assess the accuracy of thermal models, an understanding of the mechanisms and pathways by which argon diffuses in feldspars is desirable. Here we present step-heating Ar diffusion experiments conducted on feldspars with diverse compositions, structural states, and microstructural characteristics. The experiments reveal systematic variations in diffusive behavior that appear closely related to these variables, with apparent closure temperatures for 0.1–1 mm grains of ~200–400 °C (assuming a 10 °C/Ma cooling rate). Given such variability, there is no broadly applicable set of diffusion parameters that can be utilized in feldspar thermal modeling; sample-specific data are required. Diffusion experiments conducted on oriented cleavage flakes do not reveal directionally-dependent diffusive anisotropy to within the resolution limits of our approach (approximately a factor of 2). Additional experiments aimed at constraining the physical significance of the diffusion domain are presented and indicate that unaltered feldspar crystals with or without coherent exsolution lamellae diffuse at the grain-scale, whereas feldspars containing hydrothermal alteration and/or incoherent sub-grain intergrowths do not. Arrhenius plots for argon diffusion in plagioclase and alkali feldspars appear to reflect a confluence of intrinsic diffusion kinetics and structural transitions that occur during incremental heating experiments. These structural transitions, along with sub-grain domain size variations, cause deviations from linearity (i.e., upward and downward curvature) on Arrhenius plots. An atomistic model for Arrhenius behavior is proposed that incorporates the variable lattice deformations of different feldspars in response to heating and

  2. Systematic variations of argon diffusion in feldspars and implications for thermochronometry

    DOE PAGES

    Cassata, William S.; Renne, Paul R.

    2013-03-07

    Coupled information about the time-dependent production and temperature-dependent diffusion of radiogenic argon in feldspars can be used to constrain the thermal evolution attending a host of Earth and planetary processes. To better assess the accuracy of thermal models, an understanding of the mechanisms and pathways by which argon diffuses in feldspars is desirable. Here we present step-heating Ar diffusion experiments conducted on feldspars with diverse compositions, structural states, and microstructural characteristics. The experiments reveal systematic variations in diffusive behavior that appear closely related to these variables, with apparent closure temperatures for 0.1–1 mm grains of ~200–400 °C (assuming a 10more » °C/Ma cooling rate). Given such variability, there is no broadly applicable set of diffusion parameters that can be utilized in feldspar thermal modeling; sample-specific data are required. Diffusion experiments conducted on oriented cleavage flakes do not reveal directionally-dependent diffusive anisotropy to within the resolution limits of our approach (approximately a factor of 2). Additional experiments aimed at constraining the physical significance of the diffusion domain are presented and indicate that unaltered feldspar crystals with or without coherent exsolution lamellae diffuse at the grain-scale, whereas feldspars containing hydrothermal alteration and/or incoherent sub-grain intergrowths do not. Arrhenius plots for argon diffusion in plagioclase and alkali feldspars appear to reflect a confluence of intrinsic diffusion kinetics and structural transitions that occur during incremental heating experiments. These structural transitions, along with sub-grain domain size variations, cause deviations from linearity (i.e., upward and downward curvature) on Arrhenius plots. An atomistic model for Arrhenius behavior is proposed that incorporates the variable lattice deformations of different feldspars in response to heating and

  3. Using Neutron Diffraction to Determine the Low-Temperature Behavior of Pb2+ in Lead Feldspar

    NASA Astrophysics Data System (ADS)

    Kolbus, L. M.; Anovitz, L. M.; Chakoumackos, B. C.; Wesolowski, D. J.

    2014-12-01

    Feldspar minerals comprise 60% of the Earth's crust, so it imperative that the properties of feldspar be well understood for seismic modeling. The structure of feldspar consists of a three-dimensional framework of strongly-bonded TO4 tetrahedra formed by the sharing of oxygen atoms between tetrahedra. The main solid solution series found in natural feldspars are alkali NaAlSi3O8 -KAlSi3O8 and plagioclase CaAl2Si2O8-NaAlSi3O8. Recently, efforts have been made to systematically quantify feldspars structural change at non-ambient temperatures by considering only the relative tilts of the tetrahedral framework [1]. This serves as a tool to predict various behaviors of the structure such as the relative anisotropy of unit cell parameters and volume evolution with composition and temperature. Monoclinic feldspars are well predicted by the model [1], but discrepancies still remain between the model predictions and real structures with respect to absolute values of the unit cell parameters. To improve the existing model, a modification must be made to account for the M-cation interaction with its surrounding oxygen atoms. We have, therefore, chosen to study the structure of Pb-feldspar (PbAl2Si2O8), which provides the opportunity to characterize a monoclinic Al2Si2 feldspar containing a large M-site divalent cation using neutron diffraction. Neutron diffraction allows for the characterization of the M-site cation interaction between the oxygen atoms in the polyhedral cage by providing information to accurately determine the atomic displacement parameters.. Lead feldspar was synthesized for this study using the method described in [2], and confirmed to have a monoclinic C2/m space group. In this talk we will present structural determinations and atomic displacement parameters of Pb-feldspar from 10 - 300K generated from Neutron diffraction at the POWGEN beamline at the Spallation Neutron Source at Oak Ridge National lab, and compare our results to those predicted by the

  4. Differential rates of feldspar weathering in granitic regoliths

    USGS Publications Warehouse

    White, A.F.; Bullen, T.D.; Schulz, M.S.; Blum, A.E.; Huntington, T.G.; Peters, N.E.

    2001-01-01

    Differential rates of plagioclase and K-feldspar weathering commonly observed in bedrock and soil environments are examined in terms of chemical kinetic and solubility controls and hydrologic permeability. For the Panola regolith, in the Georgia Piedmont Province of southeastern United States, petrographic observations, coupled with elemental balances and 87Sr/86Sr ratios, indicate that plagioclase is being converted to kaolinite at depths > 6 m in the granitic bedrock. K-feldspar remains pristine in the bedrock but subsequently weathers to kaolinite at the overlying saprolite. In contrast, both plagioclase and K-feldspar remain stable in granitic bedrocks elsewhere in Piedmont Province, such as Davis Run, Virginia, where feldspars weather concurrently in an overlying thick saprolite sequence. Kinetic rate constants, mineral surface areas, and secondary hydraulic conductivities are fitted to feldspar losses with depth in the Panola and Davis Run regoliths using a time-depth computer spreadsheet model. The primary hydraulic conductivities, describing the rates of meteoric water penetration into the pristine granites, are assumed to be equal to the propagation rates of weathering fronts, which, based on cosmogenic isotope dating, are 7 m/106 yr for the Panola regolith and 4 m/106 yr for the Davis Run regolith. Best fits in the calculations indicate that the kinetic rate constants for plagioclase in both regoliths are factors of two to three times faster than K-feldspar, which is in agreement with experimental findings. However, the range for plagioclase and K-feldspar rates (kr = 1.5 x 10-17 to 2.8 x 10-16 mol m-2 s-1) is three to four orders of magnitude lower than for that for experimental feldspar dissolution rates and are among the slowest yet recorded for natural feldspar weathering. Such slow rates are attributed to the relatively old geomorphic ages of the Panola and Davis Run regoliths, implying that mineral surface reactivity decreases significantly with

  5. Partition coefficients for calcic plagioclase - Implications for Archean anorthosites

    NASA Technical Reports Server (NTRS)

    Phinney, W. C.; Morrison, D. A.

    1990-01-01

    In most Archean cratons, cumulates of equant plagioclase megacrysts form anorthositic complexes, including those at Bad Vermilion Lake (Ontario). In this paper, partition coefficients (Ds) of REEs between natural high-Ca plagioclase megacrysts and their basaltic matrices were determined, using a multiple aliquot techique, and megacrystic plagioclases occurring in anorthosites were analyzed for the same components which, in conjunction with their Ds, were applied to calculations of melts in equilibrium with anorthosites. The REE's Ds were found to agree well with experimentally determined values and to predict equilibrium melts for Archean anorthosites that agree well with coeval basaltic flows and dikes. The Ds also appear to be valid for both the tholeiitic and alkali basalts over a wide range of mg numbers and REE concentrations. It is suggested that the moderately Fe-rich tholeiites that are hosts to plagioclase megacrysts in greenstone belts form the parental melts for megacrysts which make up the Bad Vermilion Lake Archean anorthositic complex.

  6. Residence times of alkali feldspar phenocrysts from magma feeding the Agnano-Monte Spina Eruption (4.7 ka), Campi Flegrei caldera (Napoli, southern Italy) based on Ba-zonation modelling

    NASA Astrophysics Data System (ADS)

    Iovine, Raffaella Silvia; Wörner, Gerhard; Carmine Mazzeo, Fabio; Arienzo, Ilenia; Fedele, Lorenzo; Civetta, Lucia; D'Antonio, Massimo; Orsi, Giovanni

    2016-04-01

    Timescales governing the development of crustal magma reservoirs are a key for understanding magmatic processes such as ascent, storage and mixing event. An estimate of these timescales can provide important constraints for volcanic hazard assessment of active volcanoes. We studied the Agnano-Monte Spina eruption (A-MS; 4.7 ka; VEI = 4; 0.85 km3 D.R.E. of magma erupted) of the Campi Flegrei caldera, one of the most dangerous volcanic areas on Earth. The A-MS eruption has been fed by magmas varying from more to less evolved trachyte whose variable 87Sr/86Sr and trace elements features suggest magma mixing between two end-members. Ba zonation profiles of alkali feldspar phenocrysts have been determined through combined energy-dispersive and wavelength-dispersive electron microprobe analyses (EDS-WDS-EMPA). We focused on distinct compositional breaks near the rim of the crystals that likely represent the last mixing event prior to eruption. We always chose the steepest gradients close to the crystal rims, taking into account that any effects related to cutting angles or crystal orientation should give longer apparent diffusion times. Two different approaches were undertaken: (1) a quantitative Ba compositional profiles were measured by point analyses along a short transect crossing growth discontinuities and (2) grey-scale profiles were taken parallel to the acquired point profiles. Assuming that Ba dominates the backscattered electron intensities in sanidines, greyscale gradients can be used as a diffusive tracer. BSE images were processed using the ImageJ® software, in order to extract a numerical greyscale profile. In both cases, each profile was interpolated through a non-linear Boltzmann fit curve with the Mathematica® software. A few traverses done at angles smaller than 90° to the compositional boundary interface were corrected by multiplying the distance values by the sinus of the traverse angle relative to the vertical on the interface. Our preliminary

  7. Plagioclase-Hosted Magnetite Inclusions From the Bushveld Complex

    NASA Astrophysics Data System (ADS)

    Feinberg, J. M.; Scott, G. R.; Renne, P. R.; Wenk, H.

    2004-12-01

    Gabbros from the Main Zone of the 2.064 Ga Bushveld Complex have long been known to possess unusually stable magnetizations due to the presence of high coercivity, exsolved magnetite inclusions in plagioclase and clinopyroxene. The paleomagnetic pole for these rocks has been used to anchor apparent polar wander paths for the Kaapval craton during the Early-Mid Proterozoic. To better understand the rock magnetic properties of silicate-hosted magnetite inclusions, oriented paleomagnetic samples of gabbro were collected from quarries near Belfast and Rustenberg, South Africa, sampling the eastern and western limbs of the Complex, respectively. Plagioclase composition at both sites ranges from An55 (rims) to An65 (cores) based on optical and electron microprobe data. Four kinds of inclusions are present within the plagioclase: elongate magnetite needles, nanometer-scale magnetite particles (responsible for the "cloudy" appearance of some crystals), translucent brown hematite/ilmenite platelets, and colorless euhedral inclusions of pyroxene and/or feldspar. Magnetite inclusions are most abundant at the cores of the plagioclase crystals. Orientations of the needles and the platelets are crystallographically controlled by the silicate host. Although the elongation direction of the magnetite inclusions can occur in any of five possible orientations, only two or three of these directions dominates each plagioclase crystal. Alternating field demagnetization of bulk samples (NRM = 1.5 x 101 A m-1) shows univectorial remanence with average median destructive fields (MDF) of 115 mT (Belfast) and 90 mT (Rustenberg). AF demagnetization of single plagioclase crystals (NRM = 100 A m-1) also shows single component remanence with average MDFs >150 mT. The NRM coercivity spectra of single plagioclase crystals are indistinguishable from that of the bulk samples. When normalized to their abundance in bulk samples the magnetite-bearing plagioclase fully accounts for the NRM of Bushveld

  8. Alkali basalts and enclosed ultramafic xenoliths near Ushuaia, Tierra Del Fuego, Argentina.

    PubMed

    Acevedo, Rogelio Daniel

    2016-01-01

    At the southernmost part of Tierra del Fuego a few outcrops and erratic boulders of alkali basaltic rocks with ultramafic enclaves have been studied. Alkali basalt plugs or pipes hitherto identified are scarce, and host rocks are constituted by slates that belong to Mesozoic deposition. The petrography, texture and composition of the basalt and xenoliths were investigated by petrographic microscope and electron microprobe analysis. Xenocrysts of amphibole and alkali feldspar, phenocrysts of nepheline, olivine, spinel, phlogopite and Fe-Ti minerals (10 %) and a diversity of xenoliths, mainly lherzolitic, pyroxenite and wehrlitic nodules (15 %), but also from metamorphic rocks provenance, are contained in the basalt groundmass (75 %). This finer-grained material is made up of laths or needles of plagioclase, pyroxene, opaque minerals, apatite and glass, with intersertal, hyalopilitic and pilotaxitic. Locally, rock has an even granoblastic texture. Former amygdules are filled by analcite, zeolites, sodalite and calcite. The normative classification, based on nepheline content, conclude that this rock is an alkali basalt. The chemical classification, considering immobile elements as Zr/TiO2 versus Nb/Y indicate an alkali basalt too and plots over the TAS diagram fall in the foidite (Na-rich or nephelinite) and basanite fields. The REE patterns are fractionated (La/Yb primitive mantle normalized is approximately 30). The K-Ar isotopic technique on individual macrocrysts gave ages of 146 ± 5 Ma (amphibole) and 127 ± 4 Ma (alkali feldspar); and K-Ar whole rock datum reported 8.3 ± 0.3 Ma. Nevertheless, fertile samples show geochemical features typical of deep derived material thus, based on the position in the actual tectonic setting, indicate that the basalt is older than its isotopic age. PMID:27610313

  9. Alkali basalts and enclosed ultramafic xenoliths near Ushuaia, Tierra Del Fuego, Argentina.

    PubMed

    Acevedo, Rogelio Daniel

    2016-01-01

    At the southernmost part of Tierra del Fuego a few outcrops and erratic boulders of alkali basaltic rocks with ultramafic enclaves have been studied. Alkali basalt plugs or pipes hitherto identified are scarce, and host rocks are constituted by slates that belong to Mesozoic deposition. The petrography, texture and composition of the basalt and xenoliths were investigated by petrographic microscope and electron microprobe analysis. Xenocrysts of amphibole and alkali feldspar, phenocrysts of nepheline, olivine, spinel, phlogopite and Fe-Ti minerals (10 %) and a diversity of xenoliths, mainly lherzolitic, pyroxenite and wehrlitic nodules (15 %), but also from metamorphic rocks provenance, are contained in the basalt groundmass (75 %). This finer-grained material is made up of laths or needles of plagioclase, pyroxene, opaque minerals, apatite and glass, with intersertal, hyalopilitic and pilotaxitic. Locally, rock has an even granoblastic texture. Former amygdules are filled by analcite, zeolites, sodalite and calcite. The normative classification, based on nepheline content, conclude that this rock is an alkali basalt. The chemical classification, considering immobile elements as Zr/TiO2 versus Nb/Y indicate an alkali basalt too and plots over the TAS diagram fall in the foidite (Na-rich or nephelinite) and basanite fields. The REE patterns are fractionated (La/Yb primitive mantle normalized is approximately 30). The K-Ar isotopic technique on individual macrocrysts gave ages of 146 ± 5 Ma (amphibole) and 127 ± 4 Ma (alkali feldspar); and K-Ar whole rock datum reported 8.3 ± 0.3 Ma. Nevertheless, fertile samples show geochemical features typical of deep derived material thus, based on the position in the actual tectonic setting, indicate that the basalt is older than its isotopic age.

  10. Identification of ice nucleation active sites on feldspar dust particles.

    PubMed

    Zolles, Tobias; Burkart, Julia; Häusler, Thomas; Pummer, Bernhard; Hitzenberger, Regina; Grothe, Hinrich

    2015-03-19

    Mineral dusts originating from Earth's crust are known to be important atmospheric ice nuclei. In agreement with earlier studies, feldspar was found as the most active of the tested natural mineral dusts. Here we investigated in closer detail the reasons for its activity and the difference in the activity of the different feldspars. Conclusions are drawn from scanning electron microscopy, X-ray powder diffraction, infrared spectroscopy, and oil-immersion freezing experiments. K-feldspar showed by far the highest ice nucleation activity. Finally, we give a potential explanation of this effect, finding alkali-metal ions having different hydration shells and thus an influence on the ice nucleation activity of feldspar surfaces. PMID:25584435

  11. Identification of Ice Nucleation Active Sites on Feldspar Dust Particles

    PubMed Central

    2015-01-01

    Mineral dusts originating from Earth’s crust are known to be important atmospheric ice nuclei. In agreement with earlier studies, feldspar was found as the most active of the tested natural mineral dusts. Here we investigated in closer detail the reasons for its activity and the difference in the activity of the different feldspars. Conclusions are drawn from scanning electron microscopy, X-ray powder diffraction, infrared spectroscopy, and oil-immersion freezing experiments. K-feldspar showed by far the highest ice nucleation activity. Finally, we give a potential explanation of this effect, finding alkali-metal ions having different hydration shells and thus an influence on the ice nucleation activity of feldspar surfaces. PMID:25584435

  12. Plagioclase sub-species in Chinese loess deposits: Implications for dust source migration and past climate change

    NASA Astrophysics Data System (ADS)

    He, Tong; Liu, Lianwen; Chen, Yang; Sheng, Xuefen; Ji, Junfeng

    2016-01-01

    Plagioclase mineral sub-species in the Lingtai Section in central Chinese Loess Plateau are examined using Mineral Liberation Analyzer techniques, showing that loess and paleosol samples exhibit similar patterns in terms of plagioclase feldspar sub-species content. This suggests that both loess and paleosol units have preserved their primary Ca-bearing plagioclase compositions of loess source regions. Weighted average CaO (%) in Ca-bearing plagioclase lies within a narrow range and is equivalent to the average plagioclase composition for upper continental crust. This fact supports the hypothesis that Chinese loess deposits are the result of a thorough mixing of dust sources. The sum of Ca-bearing plagioclase content exhibits a general increasing trend superimposed by glacial-interglacial oscillations. In combination with observed plagioclase data in the deserts, the variations of Ca-bearing plagioclase minerals might be used as a proxy for dust source migration and climate changes in the loess source regions. Furthermore, linear relationship between lithogenic magnetic susceptibility (MS) component input and contents of Ca-bearing plagioclase in loess units revises a MS proxy for reconstructing paleo-monsoon precipitation history. The revised MS and plagioclase sub-species records help in understanding the mechanism of glaciation across northern Tibetan Plateau.

  13. Plagioclase flotation and lunar crust formation

    NASA Technical Reports Server (NTRS)

    Walker, D.; Hays, J. F.

    1977-01-01

    Anorthitic plagioclase floats in liquids parental to the lunar highlands crust. The plagioclase enrichment that is characteristic of lunar highlands rocks can be the result of plagioclase flotation. Such rocks would form a gravitationally stable upper crust on their parental magma.

  14. The origin of felsic microgranitoid enclaves: Insights from plagioclase crystal size distributions and thermodynamic models

    NASA Astrophysics Data System (ADS)

    Alves, Adriana; Pereira, Giovanna de Souza; Janasi, Valdecir de Assis; Higgins, Michael; Polo, Liza Angelica; Juriaans, Orlando Stanley; Ribeiro, Bruno Vieira

    2015-12-01

    Magma mixing is widely recognized in contemporary petrology as one of the primary igneous processes. Microgranitoid enclaves (MEs) are considered to be remnants of such mixing processes, and the term has a well-established genetic implication. However, microgranitoid enclaves span a wide range of compositions, and felsic varieties are also frequently reported. Nd-Sr isotope and textural data from felsic microgranitoid enclaves (FMEs), mafic microgranitoid enclaves (MMEs) and host granites from the Salto pluton, Itu Granitic Province, show that the cm-sized MMEs are dioritic, have medium-grained igneous textures and xenocrysts of alkali feldspar and quartz. The FMEs are cm- to meter-sized, have spheric shapes, show corrugated contacts with the host granites, and have resorbed feldspars and deformed quartz crystals interpreted as xenocrysts set in a fine-grained groundmass. Compared to the host granites, both MME and FME samples have increased FeO, MgO, TiO2, P2O5 and Zr contents, but their Sr and Nd isotope signatures are identical: FME 87Sr/86Sri = 0.7088-0.7063, εNdi = - 10.0 to - 10.2; MME 87Sr/86Sri = 0.7070, εNdi = - 10.5; host granite 87Sr/86Sri 0.7056-0.7060, εNdi = - 10.2 to - 10.3. These indicate that the enclaves derive from a similar source, although the melts from which they formed were probably hotter and chemically more primitive than their host granites. Crystal size distributions (CSDs) of plagioclase in samples drilled from rinds and cores of three FMEs show that the rind samples are systematically finer-grained than the samples from the cores, which indicates that the FMEs cooled inwards and contradict interpretations that the FMEs are autoliths. Thermal modeling suggests that a slightly more primitive, hotter magma would be thermally equilibrated with an evolved resident melt within weeks after mixing/mingling. Upon thermal equilibrium, the FMEs would have an increased crystal cargo, and the resulting touching framework would impart a solid

  15. Formation of halloysite from feldspar: Low temperature, artificial weathering versus natural weathering

    USGS Publications Warehouse

    Parham, W.E.

    1969-01-01

    Weathering products formed on surfaces of both potassium and plagioclase feldspar (An70), which were continuously leached in a Soxhlet extraction apparatus for 140 days with 7.21 of distilled water per day at a temperature of approximately 78 ??C, are morphologically identical to natural products developed on potassium feldspars weathered under conditions of good drainage in the humid tropics. The new products, which first appear as tiny bumps on the feldspar surface, start to develop mainly at exposed edges but also at apparently random sites on flat cleavage surfaces. As weathering continues, the bumps grow outward from the feldspar surface to form tapered projections, which then develop into wide-based thin films or sheets. The thin sheets of many projections merge laterally to form one continuous flame-shaped sheet. The sheets formed on potassium feldspars may then roll to form tubes that are inclined at a high angle to the feldspar surface. Etch pits of triangular outline on the artificially weathered potassium feldspars serve as sites for development of continuous, non-rolled, hollow tubes. It is inferred from its morphology that this weathering product is halloysite or its primitive form. The product of naturally weathered potassium feldspars is halloysite . 4H2O. The flame-shaped films or sheets formed on artificially weathered plagioclase feldspar do not develop into hollow tubes, but instead give rise to a platy mineral that is most probably boehmite. These plates form within the flame-shaped films, and with continued weathering are released as the film deteriorates. There is no indication from this experiment that platy pseudohexagonal kaolinite forms from any of these minerals under the initial stage of weathering. ?? 1969.

  16. Crystallography of some lunar plagioclases

    USGS Publications Warehouse

    Stewart, D.B.; Appleman, D.E.; Huebner, J.S.; Clark, J.R.

    1970-01-01

    Crystals of calcic bytownite from type B rocks have space group U with c ??? 14 angstroms. Bytownite crystals from type A rocks are more sodic and have space group C1, c ??? 7 angstroms. Cell parameters of eight bulk feldspar separates from crystalline rocks indicate that the range of angle gamma is about 23 times the standard error of measurement, and its value might be useful for estimation of composition. Cell parameters of seven ilmenites are close to those of pure FeTiO3.

  17. Laser Raman Spectroscopic Characterization of Shocked Plagioclase from the Lonar Impact Crater, India.

    NASA Astrophysics Data System (ADS)

    Chakrabarti, R.; Basu, A. R.; Peterson, J.; Misra, S.

    2004-12-01

    We report Raman spectra of shocked plagioclase grains from the Lonar impact Crater of India. The Lonar Crater, located in the Buldana district of Maharashtra, India (19° 58'N, 76° 31'E), is an almost circular depression in the 65Ma old basalt flows of the Deccan Traps. Age estimates of this impact crater range from 10-50ka. Tektite and basalt samples were collected for this study from the rim of the crater, which is raised about 20 meters above the surrounding plains. For comparison, a Manicouagan maskelynite and an unaltered mid-oceanic ridge basalt with plagioclase laths were also analyzed. Polished thin sections of all these samples were first petrographically studied. The MORB plagioglase as well as the plagioclase from Lonar host-basalts show first order interference colors and distinct multiple lamellar twinning. The Manicouagan maskelynite is isotropic under crossed-polars. The Lonar tektite samples characteristically demonstrate spherules which are identified by their perfectly circular cross-section and isotropic nature. The spherules also contain fragments of the host basalt with plagioclase laths showing lamellar twinning. The groundmass within the spherules shows lath shaped plagioclase grains, most of which show varying degrees of isotropism due to maskelynitization. Raman scattering measurements were performed using the 514.5 nm line of an argon ion laser at an intensity of 40 kW/cm2. An inverted microscope (Nikon TE3000) with 50x objective (NA 0.55) was used for confocal imaging. A holographic notch filter removed residual laser scatter and the Raman scattering was detected by a silicon CCD at -90° C (Princeton Instruments Spec10-400R). Raman spectra were collected from ~250 cm-1 through 2000 cm-1. Raman spectra of crystalline unshocked plagioclase feldspars from the MORB and the Lonar host basalt show strongest peaks at 265 cm-1, 410 cm-1, 510 cm-1 and 1110 cm-1. The results remain the same for different points in a single grain but vary slightly

  18. Feldspars Detected by ChemCam in Gale Crater with Implications for Future Martian Exploration

    NASA Astrophysics Data System (ADS)

    Gasda, P. J.; Carlson, E.; Wiens, R. C.; Bridges, J.; Sautter, V.; Cousin, A.; Maurice, S.; Gasnault, O.; Clegg, S. M.

    2015-12-01

    Feldspar is a common igneous mineral that can shed light on parent magma temperatures, pressures, and compositions. During the first 801 sols of the NASA Mars Science Laboratory mission, we have detected 125 possible feldspar grains using the ChemCam LIBS instrument. We analyzed spectra from successive laser shots at the same location and approximate whole rock compositions for each target. Feldspar-containing targets range from tephrite-basanite to trachyandesite. The most common feldspar type is andesine; no targets are >An60. Over 30% are anorthoclase, and ~10% have potassium contents up to Or60. Individual shot measurements in a single spot suggest some feldspars are zoned. Most of these rocks are either float or incorporated into conglomerates, and thus we do not know their provenance. Many of the samples may originate from the Gale crater walls, indicative of Southern Highland ancient crust. Some may also be flung from further away (e.g., emplaced by impact processes). Hence, these rocks may give us a general clue to the variety of evolved igneous materials on Mars. The ubiquity of feldspars at Gale suggests that they have been significantly underestimated for the Southern Highlands, if not for the whole of Mars. For example, significant abundance of andesitic feldspars in both the southern highland and northern lowlands of Mars would imply that Martian volcanism has produced a greater extent of evolved igneous materials to a greater degree than previously thought. Remote sensing instruments are insensitive to plagioclase due to dust cover, lack of exposures, or low feldspar FeO content. However, the Mars 2020 rover will be equipped with 3 new instruments, the arm-mounted SHERLOC Raman, PIXL μXRF, and the mast-mounted SuperCam combined Raman-LIBS instruments, which should help characterize Martian feldspars. Additionally, the SuperCam instrument plans to include three feldspars in its suite of 20+ onboard standards to improve feldspar chemical analysis.

  19. Origin of strongly reversed rims on plagioclase in cumulates

    NASA Astrophysics Data System (ADS)

    Morse, S. A.; Nolan, Kathleen M.

    1984-06-01

    Narrow reversed rims on plagioclase are ubiquitous in troctolites and olivine gabbros of the Kiglapait intrusion and may be a common feature of all such cumulates. The rims occur at plag/plag, plag/ol, and less strongly at plag/aug grain boundaries. They are optically obvious at ΔAn < 10 mol.% and can reach ΔAn = 32 mol.% or more. In parallel, K/Na drops sharply. Although ubiquitous from sample to sample, the reversed rims are only locally present at grain boundaries even for the same pair of crystals in contact; they are prominent in linear networks suggesting the last trace of intercumulus liquid. A subsolidus origin is ruled out by the absence of reactants at plag/plag and plag/ol boundaries and by the local rather than pervasive development of rims. The rims are required to grow from intercumulus liquid, in which the partition of An component between crystals and liquid increases with the trapped augite component of the liquid. Calculations from published experimental data show that ΔAn > 30 can easily be achieved by such a process. It is also probable that the trapped liquid is part of an An-rich boundary layer generated by solute rejection during adcumulus growth. The ability of the rims to sustain steep K/Na gradients despite a long subsolidus cooling history proves that the K sbnd Na exchange rate is vanishingly small over a geologic time scale in An-rich feldspar, suggesting that at low K content the potassium is site-bound to the tetrahedral Al/Si distribution. Reversed rims therefore provide important information on diffusion limits as well as on the late-stage solidification history of plagioclase-rich cumulates. Moreover, they demonstrate that plagioclase geothermometry cannot be divorced from effects of liquid composition and structure as monitored, for example, by augite content.

  20. Chemical Zoning of Feldspars in Lunar Granitoids: Implications for the Origins of Lunar Silicic Magmas

    NASA Technical Reports Server (NTRS)

    Mills, R. D; Simon, J. I.; Alexander, C.M. O'D.; Wang, J.; Christoffersen, R.; Rahman, Z..

    2014-01-01

    Fine-scale chemical and textural measurements of alkali and plagioclase feldspars in the Apollo granitoids (ex. Fig. 1) can be used to address their petrologic origin(s). Recent findings suggest that these granitoids may hold clues of global importance, rather than of only local significance for small-scale fractionation. Observations of morphological features that resemble silicic domes on the unsampled portion of the Moon suggest that local, sizable net-works of high-silica melt (>65 wt % SiO2) were present during crust-formation. Remote sensing data from these regions suggest high concentrations of Si and heat-producing elements (K, U, and Th). To help under-stand the role of high-silica melts in the chemical differentiation of the Moon, three questions must be answered: (1) when were these magmas generated?, (2) what was the source material?, and (3) were these magmas produced from internal differentiation. or impact melting and crystallization? Here we focus on #3. It is difficult to produce high-silica melts solely by fractional crystallization. Partial melting of preexisting crust may therefore also have been important and pos-sibly the primary mechanism that produced the silicic magmas on the Moon. Experimental studies demonstrate that partial melting of gabbroic rock under mildly hydrated conditions can produce high-silica compositions and it has been suggested by that partial melting by basaltic underplating is the mechanism by which high-silica melts were produced on the Moon. TEM and SIMS analyses, coordinated with isotopic dating and tracer studies, can help test whether the minerals in the Apollo granitoids formed in a plutonic setting or were the result of impact-induced partial melting. We analyzed granitoid clasts from 3 Apollo samples: polymict breccia 12013,141, crystalline-matrix breccia 14303,353, and breccia 15405,78

  1. Investigation of Plagioclase Reactivity in Wet Supercritical CO2 by In Situ Infrared Spectroscopy

    NASA Astrophysics Data System (ADS)

    Thompson, C.; Gauglitz, K.; Loring, J.; Schaef, T.; Miller, Q.; Johnson, K. T.; Wang, Z.; Rosso, K. M.; McGrail, P.

    2013-12-01

    Increasingly, CO2 capture and subsequent storage in deep geologic reservoirs is being implemented as a viable approach for reducing anthropogenic emissions of CO2 into the atmosphere. Several mechanisms may act to secure the injected CO2, including hydrodynamic confinement, dissolution into reservoir fluids, retention of CO2 as a separate phase in pore spaces, and carbonation of reservoir minerals. This latter mechanism is the most permanent, but it requires the presence of reactive minerals and potentially significant amounts of time for the reactions to proceed. Plagioclase feldspars are highly abundant in the earth's crust and are present in the caprocks and storage formations of many target reservoirs. Although the dissolution kinetics and carbonation reactions of feldspars have been well studied in the aqueous phase, comparatively little work has focused on plagioclase reactivity in the CO2-rich fluid at conditions relevant to geologic carbon sequestration. In this study, we used in situ infrared spectroscopy to investigate the carbonation potential of a powdered plagioclase sample similar to labradorite [(Ca,Na)(Al,Si)4O8] that had been isolated from a Hawaiian basalt. Experiments were carried out at 50 °C and 91 bar by circulating a stream of dry or wet supercritical CO2 (scCO2) past a sample overlayer deposited on the window of a high-pressure infrared flow cell. Water concentrations ranged from 0% to 125% relative to saturation, and transmission-mode absorbance spectra were recorded as a function of time for 24 hours. In experiments with excess water, a controlled temperature gradient was used to intentionally condense a film of liquid water on the overlayers' surfaces. No discernible reaction was detected when the samples were exposed to anhydrous scCO2. When water was added, a thin film of liquid-like water was observed on the samples' surfaces, and up to 0.3% of the plagioclase was converted to a carbonate phase. Calcite is the most likely reaction

  2. Water Content of Lunar Alkali Fedlspar

    NASA Technical Reports Server (NTRS)

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

    2016-01-01

    Detection of indigenous hydrogen in a diversity of lunar materials, including volcanic glass, melt inclusions, apatite, and plagioclase suggests water may have played a role in the chemical differentiation of the Moon. Spectroscopic data from the Moon indicate a positive correlation between water and Th. Modeling of lunar magma ocean crystallization predicts a similar chemical differentiation with the highest levels of water in the K- and Th-rich melt residuum of the magma ocean (i.e. urKREEP). Until now, the only sample-based estimates of water content of KREEP-rich magmas come from measurements of OH, F, and Cl in lunar apatites, which suggest a water concentration of < 1 ppm in urKREEP. Using these data, predict that the bulk water content of the magma ocean would have <10 ppm. In contrast, estimate water contents of 320 ppm for the bulk Moon and 1.4 wt % for urKREEP from plagioclase in ferroan anorthosites. Results and interpretation: NanoSIMS data from granitic clasts from Apollo sample 15405,78 show that alkali feldspar, a common mineral in K-enriched rocks, can have approx. 20 ppm of water, which implies magmatic water contents of approx. 1 wt % in the high-silica magmas. This estimate is 2 to 3 orders of magnitude higher than that estimated from apatite in similar rocks. However, the Cl and F contents of apatite in chemically similar rocks suggest that these melts also had high Cl/F ratios, which leads to spuriously low water estimates from the apatite. We can only estimate the minimum water content of urKREEP (+ bulk Moon) from our alkali feldspar data because of the unknown amount of degassing that led to the formation of the granites. Assuming a reasonable 10 to 100 times enrichment of water from urKREEP into the granites produces an estimate of 100-1000 ppm of water for the urKREEP reservoir. Using the modeling of and the 100-1000 ppm of water in urKREEP suggests a minimum bulk silicate Moon water content between 2 and 20 ppm. However, hydrogen loss was

  3. Mineral resource of the month: feldspar

    USGS Publications Warehouse

    Potter, Michael J.

    2004-01-01

    The United States is the third leading producer of feldspar worldwide, after Italy and Turkey, according to data published by the U.S. Geological Survey. Foreign analysts indicate that China is also a leading feldspar producer, but official production data are not available. Feldspars are aluminum silicate minerals that contain varying proportions of calcium, potassium and sodium. Usually occurring in igneous rocks, feldspars are estimated to constitute 60 percent of Earth’s crust.

  4. Microbial extracellular polysaccharides and plagioclase dissolution

    NASA Astrophysics Data System (ADS)

    Welch, S. A.; Barker, W. W.; Banfield, J. F.

    1999-05-01

    Bytownite feldspar was dissolved in batch reactors in solutions of starch (glucose polymer), gum xanthan (glucose, mannose, glucuronic acid), pectin (poly-galacturonic acid), and four alginates (mannuronic and guluronic acid) with a range of molecular weights (low, medium, high and uncharacterized) to evaluate the effect of extracellular microbial polymers on mineral dissolution rates. Solutions were analyzed for dissolved Si and Al as an indicator of feldspar dissolution. At neutral pH, feldspar dissolution was inhibited by five of the acid polysaccharides, gum xanthan, pectin, alginate low, alginate medium, alginate high, compared to an organic-free control. An uncharacterized alginate substantially enhanced both Si and Al release from the feldspar. Starch, a neutral polysaccharide, had no apparent effect. Under mildly acidic conditions, initial pH ≈ 4, all of the polymers enhanced feldspar dissolution compared to the inorganic controls. Si release from feldspar in starch solution exceeded the control by a factor of three. Pectin and gum xanthan increased feldspar dissolution by a factor of 10, and the alginates enhanced feldspar dissolution by a factor of 50 to 100. Si and Al concentrations increased with time, even though solutions were supersaturated with respect to several possible secondary phases. Under acidic conditions, initial pH ≈ 3, below the pK a of the carboxylic acid groups, dissolution rates increased, but the relative increase due to the polysaccharides is lower, approximately a factor of two to ten. Microbial extracellular polymers play a complex role in mineral weathering. Polymers appear to inhibit dissolution under some conditions, possibly by irreversibly binding to the mineral surfaces. The extracellular polysaccharides can also enhance dissolution by providing protons and complexing with ions in solution.

  5. Reflectance properties of spinel-plagioclase mixtures

    NASA Astrophysics Data System (ADS)

    Cheek, L.; Jackson, C.; Dhingra, D.; Pieters, C. M.; Prissel, T. C.; Williams, K. B.

    2012-12-01

    Near-infrared spectra displaying the diagnostic properties of Mg-spinel have recently been reported in several lunar craters based on Moon Mineralogy Mapper (M3) data [1-5]. These spectra lack evidence for olivine or pyroxene, suggesting that they represent a spinel-plagioclase lithology [1]. Current hypotheses [6, 7] suggest that this lithology formed by interactions of a mafic or ultramafic liquid with an anorthositic country rock, but the proportions of spinel and plagioclase are unknown. The aim of this work is to constrain the modal abundances of spinel and plagioclase in the observed lithology using laboratory reflectance spectroscopy of particulate mixtures. Reflectance spectra of Mg-spinel display a strong absorption at ~2000 nm due to Fe2+ in a tetrahedral site [e.g., 8]. At higher FeO contents, > ~5 wt%, an octahedral absorption near 1000 nm is also apparent [9]. Plagioclase often displays a broad absorption centered near 1250 nm due to trace amounts (0.1 wt%) of Fe2+ in the Ca2+ site. Previous studies have noted that plagioclase must be present in extremely high abundances (~85 vol%) in order for the 1250 nm absorption to be apparent in mixtures with olivine and pyroxene [10, 11]. Recent nonlinear modeling has suggested that at least 50% plagioclase is necessary for the 1250 nm absorption to be apparent in a calculated mixture with spinel [12]. Our approach involves making mineral mixtures of spinel and plagioclase particulate samples and measuring near-infrared spectra of the bulk material. For the plagioclase endmember, we use terrestrial gem quality labradorite with ~0.3 wt% FeO. The spinel endmember was produced experimentally at Brown University (1500 C; fO2~ IW; sintered 72 hrs), and contains 5 wt% FeO. Preliminary results show that spectra of a 90% plagioclase - 10% spinel mixture only display the spectral properties of the spinel component; the 1250 nm absorption is not apparent. Importantly, the addition of 90% plagioclase does not significantly

  6. Energy related studies utilizing K-feldspar thermochronology

    SciTech Connect

    Not Available

    1993-01-01

    Two distinct sources of information are available from a [sup 40]Ar/[sup 39]Ar step-heating experiment: the age spectrum and Arrhenius plot. Model ages are calculated from the flux of radiogenic argon ([sup 40]Ar*) (assuming trapped argon of atmospheric composition) relative to the reactor produced [sup 39]Ar evolved during discrete laboratory heating steps. With the additional assumption that the [sup 39]Ar is uniformly distributed within the sample, we can infer the spatial distribution of the daughter product. ne associated Arrhenius plot, derived by plotting the diffusion coefficient (obtained from the inversion of the 39[sup Ar] release function assuming a single domain) against the inverse temperature of laboratory heating, are a convolution of the parameters which characterize the individual diffusion domains (whether these be dictated by varying length scale, energetics, etc.). However, many and perhaps Most [sup 40]Ar/[sup 39]Ar age spectra for slowly cooled alkali feldspars are significantly different from model age spectra calculated assuming a single diffusion-domain size. In addition, Arrhenius plots calculated from the measured loss of [sup 39]Ar during the step heating experiment show departures from linearity that are inconsistent with diffusion from domains of equal size. By extending the single diffusion-domain closure model (Dodsontype) to apply to minerals with a discrete distribution of domain sizes, we obtained an internally consistent explanation for the commonly observed features of alkali feldspar age spectra and their associated Arrhenius plots.

  7. Plagioclase mineralogy of olivine alkaline basalt

    NASA Technical Reports Server (NTRS)

    Hoffer, J. M.

    1973-01-01

    A geological and mineralogical study of the Potrillo volcanics is reported. The investigation consisted first of field mapping to establish and identify the different rock types and volcanic features in order to determine the geological history. Next, samples were collected and analyzed petrographically to determine suitable rocks from the various stratigraphic units for study of plagioclase. Samples selected for further study were crushed and the plagioclase extracted for the determination of composition and structural state. These results were then related to the petrology and crystallization of the basalt.

  8. Rock-Forming feldspars of the Khibiny alkaline pluton, Kola Peninsula, Russia

    NASA Astrophysics Data System (ADS)

    Ivanyuk, G. Yu.; Pakhomovsky, Ya. A.; Konopleva, N. G.; Kalashnikov, A. O.; Korchak, Yu. A.; Selivanova, E. A.; Yakovenchuk, V. N.

    2010-12-01

    This paper describes the structural-compositional zoning of the well-known Khibiny pluton in regard to rock-forming feldspars. The content of K-Na-feldspars increases inward and outward from the Main foidolite ring. The degree of coorientation of tabular K-Na-feldspar crystals sharply increases in the Main ring zone, and microcline-dominant foyaite turns into orthoclase-dominant foyaite. The composition of K-Na-feldspars in the center of the pluton and the Main ring zone is characterized by an enrichment in Al. This shift is compensated by a substitution of some K and Na with Ba (the Main ring zone) or by an addition of K and Na cations to the initially cation-deficient microcline (the central part of the pluton). Feldspars of volcanosedimentary rocks occurring as xenoliths in foyaite primarily corresponded to plagioclase An15-40, but high-temperature fenitization and formation of hornfels in the Main ring zone gave rise to the crystallization of anorthoclase subsequently transformed into orthoclase and albite due to cooling and further fenitization. Such a zoning is the result of filling the Main ring fault zone within the homogeneous foyaite pluton with a foidolite melt, which provided the heating and potassium metasomatism of foyaite and xenoliths of volcanosedimentary rocks therein. The process eventually led to the transformation of foyaite into rischorrite-lyavochorrite, while xenoliths were transformed into aluminum hornfels with anorthoclase, annite, andalusite, topaz, and sekaninaite.

  9. Exchange of Na+ and K+ between water vapor and feldspar phases at high temperature and low vapor pressure

    USGS Publications Warehouse

    Fournier, R.O.

    1976-01-01

    In order to determine whether gas (steam) containing a small amount of dissolved alkali chloride is effective in promoting base exchange of Na+ and K+ among alkali feldspars and coexisting brine or brine plus solid salt, experiments were carried out at 400-700??C and steam densities ranging down to less than 0.05. For bulk compositions rich in potassium, the low pressure results are close to previous high-pressure results in composition of the fluid and coexisting solid phase. However, when the bulk composition is more sodic, alkali feldspars are relatively richer in potassium at low pressure than at high pressure. This behaviour corresponds to enrichment of potassium in the gas phase relative to coexisting brine and precipitation of solid NaCl when the brine plus gas composition becomes moderately sodic. The gas phase is very effective in promoting base exchange between coexisting alkali feldspars at high temperature and low water pressure. This suggests that those igneous rocks which contain coexisting alkali feldspars out of chemical equilibrium either remained very dry during the high-temperature part of their cooling history or that the pore fluid was a gas containing very little potassium relative to sodium. ?? 1976.

  10. Mineral resource of the month: feldspar

    USGS Publications Warehouse

    ,

    2011-01-01

    The article focuses on feldspar, a mineral that composes of potassium, sodium, or a fusion of the two, and its various applications. According to estimates by scientists, the mineral is present at 60 percent of the crust of Earth, wherein it is commonly used for making glass and ceramics. Global mining of feldspar was about 20 million metric tons in 2010, wherein Italy, Turkey, and China mine 55 percent of the feldspar worldwide.

  11. Effects of shock pressures on calcic plagioclase

    NASA Technical Reports Server (NTRS)

    Gibbons, R. V.; Ahrens, T. J.

    1977-01-01

    Calcic plagioclase single crystals were subjected to shock loading up to a pressure of 496 kbar; optical and electron microscope studies were conducted to investigate the shock-induced effects on the mineral, which is found in terrestrial and lunar rocks and in meteorites. It was observed that up to 287 kbar pressure, the recovered samples are essentially crystalline, while samples subjected to pressures between 300 and 400 kbar are almost 100% diaplectic glasses, suggesting shock transformation in the solid state. Samples shock-loaded to pressures greater than 400 kbar yielded glasses with refractive indices similar to those of thermally fused glass. It is concluded that planar features, absent in all the specimens, may not be definitive shock indicators, but may be linked to local heterogeneous dynamic stresses experienced by plagioclase grains within shocked rocks.

  12. Feldspar dissolution rates in the Topopah Spring Tuff, Yucca Mountain, Nevada

    USGS Publications Warehouse

    Bryan, C.R.; Helean, K.B.; Marshall, B.D.; Brady, P.V.

    2009-01-01

    Two different field-based methods are used here to calculate feldspar dissolution rates in the Topopah Spring Tuff, the host rock for the proposed nuclear waste repository at Yucca Mountain, Nevada. The center of the tuff is a high silica rhyolite, consisting largely of alkali feldspar (???60 wt%) and quartz polymorphs (???35 wt%) that formed by devitrification of rhyolitic glass as the tuff cooled. First, the abundance of secondary aluminosilicates is used to estimate the cumulative amount of feldspar dissolution over the history of the tuff, and an ambient dissolution rate is calculated by using the estimated thermal history. Second, the feldspar dissolution rate is calculated by using measured Sr isotope compositions for the pore water and rock. Pore waters display systematic changes in Sr isotopic composition with depth that are caused by feldspar dissolution. The range in dissolution rates determined from secondary mineral abundances varies from 10-16 to 10-17 mol s-1 kg tuff-1 with the largest uncertainty being the effect of the early thermal history of the tuff. Dissolution rates based on pore water Sr isotopic data were calculated by treating percolation flux parametrically, and vary from 10-15 to 10-16 mol s-1 kg tuff-1 for percolation fluxes of 15 mm a-1 and 1 mm a-1, respectively. Reconciling the rates from the two methods requires that percolation fluxes at the sampled locations be a few mm a-1 or less. The calculated feldspar dissolution rates are low relative to other measured field-based feldspar dissolution rates, possibly due to the age (12.8 Ma) of the unsaturated system at Yucca Mountain; because oxidizing and organic-poor conditions limit biological activity; and/or because elevated silica concentrations in the pore waters (???50 mg L-1) may inhibit feldspar dissolution. ?? 2009 Elsevier Ltd. All rights reserved.

  13. Anorthosites and anorthosites: Contrasting plagioclase-rich rocks in the Archaean and Proterozoic

    SciTech Connect

    Owens, B.E. . Dept. of Earth Planetary Sciences)

    1993-03-01

    Anorthosites -- rocks consisting predominantly of plagioclase feldspar -- have figured prominently in at least two distinct intervals of Earth history: the late-Archaean and mid-Proterozoic. Archaean anorthosites (AA) are a key component of high-grade gneiss terranes, where they typically form laterally extensive deformed sheets or sills up to a km thick. In contrast, Proterozoic anorthosites (PA) form plutons or plutonic complexes, and are most abundant in a quasi-continuous belt across NE N. America. In addition to these temporal and structural contrasts, AA and PA display markedly different mineralogical and geochemical properties, including, respectively: (1) equant plagioclase megacrysts vs. tabular megacrysts; (2) highly calcic compositions vs. intermediate to alkalic compositions; (3) amphibole vs. olivine or orthopyroxene as the dominant mafic mineral; (4) the presence of chromite, locally in ore-grade layers vs. massive, cross-cutting Fe-Ti oxide ores; (5) low levels of Sr and Ba vs. high to extreme levels; (6) high levels of ferromagnesian trace elements vs. low levels; (7) Ga/Al values typical of basaltic plagioclase vs. much lower values; and (8) moderately vs. extremely fractionated REE patterns. Given these contrasts, it appears that the only property AA and PA share is their plag-rich nature, suggesting that there must be more than one process (and probably multiple processes) capable of producing anorthosite.

  14. Atmospheric weathering and silica-coated feldspar: analogy with zeolite molecular sieves, granite weathering, soil formation, ornamental slabs, and ceramics.

    PubMed

    Smith, J V

    1998-03-31

    Feldspar surfaces respond to chemical, biological, and mechanical weathering. The simplest termination is hydroxyl (OH), which interacts with any adsorption layer. Acid leaching of alkalis and aluminum generated a silica-rich, nanometers-thick skin on certain feldspars. Natural K, Na-feldspars develop fragile surfaces as etch pits expand into micrometer honeycombs, possibly colonized by lichens. Most crystals have various irregular coats. Based on surface-catalytic processes in molecular sieve zeolites, I proposed that some natural feldspars lose weakly bonded Al-OH (aluminol) to yield surfaces terminated by strongly bonded Si-OH (silanol). This might explain why some old feldspar-bearing rocks weather slower than predicted from brief laboratory dissolution. Lack of an Al-OH infrared frequency from a feldspar surface is consistent with such a silanol-dominated surface. Raman spectra of altered patches on acid-leached albite correspond with amorphous silica rather than hydroxylated silica-feldspar, but natural feldspar may respond differently. The crystal structure of H-exchanged feldspar provides atomic positions for computer modeling of complex ideas for silica-terminated feldspar surfaces. Natural weathering also depends on swings of temperature and hydration, plus transport of particles, molecules, and ionic complexes by rain and wind. Soil formation might be enhanced by crushing granitic outcrops to generate new Al-rich surfaces favorable for chemical and biological weathering. Ornamental slabs used by architects and monumental masons might last longer by minimizing mechanical abrasion during sawing and polishing and by silicifying the surface. Silica-terminated feldspar might be a promising ceramic surface.

  15. Toward quantification of strain-related mosaicity in shocked lunar and terrestrial plagioclase by in situ micro-X-ray diffraction

    NASA Astrophysics Data System (ADS)

    Pickersgill, Annemarie E.; Flemming, Roberta L.; Osinski, Gordon R.

    2015-11-01

    Studies of shock metamorphism of feldspar typically rely on qualitative petrographic observations, which, while providing invaluable information, can be difficult to interpret. Shocked feldspars, therefore, are now being studied in greater detail by various groups using a variety of modern techniques. We apply in situ micro-X-ray diffraction (μXRD) to shocked lunar and terrestrial plagioclase feldspar to contribute to the development of a quantitative scale of shock deformation for the feldspar group. Andesine and labradorite from the Mistastin Lake impact structure, Labrador, Canada, and anorthite from Earth's Moon, returned during the Apollo program, were examined using optical petrography and assigned to subgroups of the optical shock level classification system of Stöffler (1971). Two-dimensional μXRD patterns from the same samples revealed increased peak broadening in the chi dimension (χ), due to strain-related mosaicity, with increased optical signs of deformation. Measurement of the full width at half maximum along χ (FWHMχ) of these peaks provides a quantitative way to measure strain-related mosaicity in plagioclase feldspar as a proxy for shock level.

  16. Evidence for the compaction of feldspar-rich cumulates in the Pleasant Bay layered intrusion, coastal Maine

    SciTech Connect

    Horrigan, E.K. )

    1993-03-01

    The Pleasant Bay intrusion is roughly 12 km by 20 km. It consists of prominent rhythmic layers, up to 100 m thick, that grade from chilled gabbro on the base, to coarse-grained gabbroic, dioritic, or granitic rocks on the top. These layers were formed by multiple injections of basalt into a large chamber of silicic magma. The focus of this study is on one layer that is about 100 m thick, and is overlain by another basally chilled gabbroic layer at least 50 m thick. Silicic pipes and veins extend upward into the overlying gabbroic chill. The lower part of the layer has dominant calcic plagioclase, An60, augite, and olivine, with subordinate hornblende and biotite. The uppermost part has dominant sodic plagioclase, An20, and two pyroxenes with subordinate quartz, K-feldspar and hornblende. SiO[sub 2] and MgO vary from 49% and 5% at the base to 58% and 1% at the top, respectively. The top 7 m of this layer are characterized by variably deformed minerals. The deformation grades from bent biotite and plagioclase near the bottom to sutured plagioclase at the top. Pockets of undeformed quartz and K-feldspar in the uppermost rocks demonstrate that interstitial liquid was present during a after compaction. The pipes and veins probably represent trapped liquid and some crystals that were expelled into the overlying gabbroic chill.

  17. Regional and local correlations of feldspar geochemistry of the Peach Spring Tuff, Alvord Mountain, California

    USGS Publications Warehouse

    Buesch, David C.

    2016-01-01

    The chemical composition of feldspar grains in an ignimbrite from the Spanish Canyon Formation in the Alvord Mountain area, California, have been used to confirm similarities in three measured sections locally, and they are similar to exposures of the Peach Spring Tuff (PST) regionally. Feldspar grains were identified on the basis of texture (zoning, as mantled feldspars, or in crystal clusters), whether the grains were attached to glass or were in pumice clasts, or were simply crystal fragments with no textural context. Chemistry was determined by electron microprobe analysis, and each analysis is calculated in terms of the percent endmember and plotted on orthoclase (Or) versus anorthite (An) plots. In general, the PST has sanidine and plagioclase compositions that are consistent with having formed in high-silica rhyolite and trachyte within a zoned magma chamber. Feldspars from the PST in Spanish Canyon area cluster along the rhyolitic trend with no grains along the trachytic trend. Similar clustering of feldspars along the rhyolitic trend with no grains along the trachytic trend also occur in the PST from Granite Spring and Providence Mountains to the east of the Alvord Mountain area, and the ranges in compositions are also similar in these locations. In contrast, the PST in the Kane Wash area of the Newberry Mountains has feldspars only from the rhyolitic trend in the basal deposits, but some grains from the trachytic trend are in the upper part of the deposit, and the range in compositions are greater than in the Spanish Canyon area. The variations in vertical compositional zoning and compositional range in these different deposits suggests there were probably different flow paths (or timing of the delivery) during the eruption and runout of the pyroclastic flow(s) generated from the climactic eruption of the PST magma chamber.

  18. Degassing driving crystallization of plagioclase phenocrysts in lava tube stalactites on Mount Etna (Sicily, Italy)

    NASA Astrophysics Data System (ADS)

    Lanzafame, Gabriele; Ferlito, Carmelo

    2014-10-01

    Basaltic lava flows can form tubes in response to the cooling of the outer surface. We collected lava stalactites (frozen lava tears) and sampled lava from the ceilings of three lava tubes on Mount Etna. Comparison of the petrographic characters between ceiling lavas and relative stalactites reveals surprising differences in the groundmass textures and crystal compositions. Major and trace element contents in stalactites show only a slight increase in alkali and SiO2 compared to ceiling lava, whereas significant differences exist in composition and textures between plagioclases within the ceiling lava and those within the stalactites, being in the last case definitively more An-rich. We advance the hypothesis that the high temperature reached in the cave caused the exsolution of the volatiles still trapped in the dripping melt. The volatiles, mainly H2O, formed bubbles and escaped from the melt; such a water-loss might have promoted the silicate polymerization in the stalactites resulting in the growth of An-rich plagioclase phenocrysts. Our results have important implications: in fact plagioclase phenocrysts are usually associated with intratelluric growth and are often considered as the main petrologic evidence for the existence of a magma chamber. The textural and chemical features of plagioclases in stalactites prove that phenocryst growth in syn to post-eruptive conditions is plausible and clearly explains the relatively low viscosity of many phenocryst-rich lava flows on Mount Etna, as well as on many other volcanoes around the world. Therefore, we can conclude that plagioclase phenocrysts cannot exclusively be considered as having originated within a magma chamber.

  19. Dissolution of K-feldspar at CO2-saturated conditions

    NASA Astrophysics Data System (ADS)

    Rosenqvist, Jörgen; Kilpatrick, Andrew D.; Yardley, Bruce W. D.; Rochelle, Christopher A.

    2014-05-01

    Underground storage of carbon dioxide on a very large scale is widely considered to be an essential part of any strategy to reduce greenhouse gas emissions to the atmosphere. Aquifers in deep sedimentary basins have been identified as suitable targets for geological carbon dioxide storage, especially aquifers located in sandstone host rock. This has led to renewed interest in studying the interaction between sandstone minerals and aqueous fluids, as there is a paucity of data for CO2-containing systems at relevant conditions. In an attempt to improve data coverage for important silicate minerals, we have measured the dissolution kinetics of K-feldspar in CO2-saturated fluids over a range of temperatures. K-feldspar fragments were hand-picked from a larger sample, crushed to a narrow size range and cleaned. The grains were reacted with water in batch-type reactors at temperatures from 20°C to 200°C and pressures up to 200 bar, and the dissolution was followed by periodic withdrawal of aliquots of solution. The mineral grains were allowed to react with pure water for a number of weeks before injection of CO2 into the system. Excess CO2 was provided to ensure CO2 saturation in the experimental systems. While the reaction time before injection was not long enough to attain complete equilibrium, it did considerably lower the degree of undersaturation with respect to K-feldspar and helped highlight the effect of CO2 injection into a rock-equilibrated aqueous fluid. At all temperatures studied, injection of CO2 resulted in a rapid increase in the soluble concentrations of K and Si (and also Na from a plagioclase component). The dissolution then reached apparent steady state conditions after a few days, with observed dissolution rates in the range of 1E-9 to 1E-12 mol/m2/s over the temperature range studied. The CO2-saturated solutions maintained mildly acidic conditions throughout the experiments and the observed rates therefore fall roughly between rates measured in

  20. Biochemical evolution II: origin of life in tubular microstructures on weathered feldspar surfaces.

    PubMed

    Parsons, I; Lee, M R; Smith, J V

    1998-12-22

    Mineral surfaces were important during the emergence of life on Earth because the assembly of the necessary complex biomolecules by random collisions in dilute aqueous solutions is implausible. Most silicate mineral surfaces are hydrophilic and organophobic and unsuitable for catalytic reactions, but some silica-rich surfaces of partly dealuminated feldspars and zeolites are organophilic and potentially catalytic. Weathered alkali feldspar crystals from granitic rocks at Shap, north west England, contain abundant tubular etch pits, typically 0.4-0.6 microm wide, forming an orthogonal honeycomb network in a surface zone 50 microm thick, with 2-3 x 10(6) intersections per mm2 of crystal surface. Surviving metamorphic rocks demonstrate that granites and acidic surface water were present on the Earth's surface by approximately 3.8 Ga. By analogy with Shap granite, honeycombed feldspar has considerable potential as a natural catalytic surface for the start of biochemical evolution. Biomolecules should have become available by catalysis of amino acids, etc. The honeycomb would have provided access to various mineral inclusions in the feldspar, particularly apatite and oxides, which contain phosphorus and transition metals necessary for energetic life. The organized environment would have protected complex molecules from dispersion into dilute solutions, from hydrolysis, and from UV radiation. Sub-micrometer tubes in the honeycomb might have acted as rudimentary cell walls for proto-organisms, which ultimately evolved a lipid lid giving further shelter from the hostile outside environment. A lid would finally have become a complete cell wall permitting detachment and flotation in primordial "soup." Etch features on weathered alkali feldspar from Shap match the shape of overlying soil bacteria.

  1. Biochemical evolution II: Origin of life in tubular microstructures on weathered feldspar surfaces

    PubMed Central

    Parsons, Ian; Lee, Martin R.; Smith, Joseph V.

    1998-01-01

    Mineral surfaces were important during the emergence of life on Earth because the assembly of the necessary complex biomolecules by random collisions in dilute aqueous solutions is implausible. Most silicate mineral surfaces are hydrophilic and organophobic and unsuitable for catalytic reactions, but some silica-rich surfaces of partly dealuminated feldspars and zeolites are organophilic and potentially catalytic. Weathered alkali feldspar crystals from granitic rocks at Shap, north west England, contain abundant tubular etch pits, typically 0.4–0.6 μm wide, forming an orthogonal honeycomb network in a surface zone 50 μm thick, with 2–3 × 106 intersections per mm2 of crystal surface. Surviving metamorphic rocks demonstrate that granites and acidic surface water were present on the Earth’s surface by ∼3.8 Ga. By analogy with Shap granite, honeycombed feldspar has considerable potential as a natural catalytic surface for the start of biochemical evolution. Biomolecules should have become available by catalysis of amino acids, etc. The honeycomb would have provided access to various mineral inclusions in the feldspar, particularly apatite and oxides, which contain phosphorus and transition metals necessary for energetic life. The organized environment would have protected complex molecules from dispersion into dilute solutions, from hydrolysis, and from UV radiation. Sub-micrometer tubes in the honeycomb might have acted as rudimentary cell walls for proto-organisms, which ultimately evolved a lipid lid giving further shelter from the hostile outside environment. A lid would finally have become a complete cell wall permitting detachment and flotation in primordial “soup.” Etch features on weathered alkali feldspar from Shap match the shape of overlying soil bacteria. PMID:9860941

  2. Uncommon behavior of plagioclase and the ancient lunar crust

    NASA Astrophysics Data System (ADS)

    Nekvasil, Hanna; Lindsley, Donald H.; DiFrancesco, Nicholas; Catalano, Tristan; Coraor, Aron E.; Charlier, Bernard

    2015-12-01

    Calcic plagioclase, the dominant mineral of the anorthositic lunar crust, fails to show the Na enrichment during cooling that is typical of magmatic plagioclase. We show that this enigmatic behavior may arise during fractionation of highly calcic plagioclase at depths greater than ~70 km in the lunar magma ocean because of the development of a negative azeotropic configuration at high anorthite contents that impedes and may even reverse the standard plagioclase albite enrichment with dropping temperature. This result supports a high-pressure origin of this plagioclase consistent with the lunar magma ocean model. It also provides a new mechanism for forming lunar lithologies with sodic plagioclase from a highly Na-depleted Moon through gravitational settling of spinel and refines the compositional characteristics of the late stage residual liquids of the lunar magma ocean.

  3. Natural radioactivity and rare earth elements in feldspar samples, Central Eastern desert, Egypt.

    PubMed

    Walley El-Dine, Nadia; El-Shershaby, Amal; Afifi, Sofia; Sroor, Amany; Samir, Eman

    2011-05-01

    The pegmatite bodies of the Eastern Desert of Egypt are widely distributed especially along the Marsa-Alam-Idfu road. The Abu Dob area covers about 150km(2) of the Arabian Nubian shield at the central part of the Eastern Desert of Egypt. Most of the pegmatite is zoned; the zonation starts with milky quartz at the core followed by alkali feldspar at the margins. The feldspars vary in color from rose to milky and in composition from K-feldspar to Na-feldspar, sometimes interactions of both types are encountered. Thirteen feldspar samples were collected from different locations in the Abu Dob area for measuring the natural radioactivity of (238)U, (232)Th and (40)K using an HPGe detector. The variation in concentration of radionuclides for the area under investigation can be classified into regions of high, medium and low natural radioactivity. The average concentration in BqKg(-1) has been observed to be from 9.5 to 183675.7BqKg(-1) for (238)U, between 6.1 and 94,314.2BqKg(-1) for (232)Th and from 0 to 7894.6BqKg(-1) for (40)K. Radium equivalent activities (Ra(eq)), dose rate (D(R)) and external hazard (H(ex)) have also been determined. In the present work, the concentration of rare earth elements are measured for two feldspar samples using two techniques, Environmental Scanning Electron microscope XIL 30 ESEM, Philips, and Inductively Coupled Plasma Mass Spectroscopy (ICP-MS). The existence of rare earth elements in this area are very high and can be used in different important industries.

  4. Natural radioactivity and rare earth elements in feldspar samples, Central Eastern desert, Egypt.

    PubMed

    Walley El-Dine, Nadia; El-Shershaby, Amal; Afifi, Sofia; Sroor, Amany; Samir, Eman

    2011-05-01

    The pegmatite bodies of the Eastern Desert of Egypt are widely distributed especially along the Marsa-Alam-Idfu road. The Abu Dob area covers about 150km(2) of the Arabian Nubian shield at the central part of the Eastern Desert of Egypt. Most of the pegmatite is zoned; the zonation starts with milky quartz at the core followed by alkali feldspar at the margins. The feldspars vary in color from rose to milky and in composition from K-feldspar to Na-feldspar, sometimes interactions of both types are encountered. Thirteen feldspar samples were collected from different locations in the Abu Dob area for measuring the natural radioactivity of (238)U, (232)Th and (40)K using an HPGe detector. The variation in concentration of radionuclides for the area under investigation can be classified into regions of high, medium and low natural radioactivity. The average concentration in BqKg(-1) has been observed to be from 9.5 to 183675.7BqKg(-1) for (238)U, between 6.1 and 94,314.2BqKg(-1) for (232)Th and from 0 to 7894.6BqKg(-1) for (40)K. Radium equivalent activities (Ra(eq)), dose rate (D(R)) and external hazard (H(ex)) have also been determined. In the present work, the concentration of rare earth elements are measured for two feldspar samples using two techniques, Environmental Scanning Electron microscope XIL 30 ESEM, Philips, and Inductively Coupled Plasma Mass Spectroscopy (ICP-MS). The existence of rare earth elements in this area are very high and can be used in different important industries. PMID:21324705

  5. Giant Plagioclase "Mosaicrysts" and Other Textures in the Steens Basalt, Columbia River Flood Basalt Province

    NASA Astrophysics Data System (ADS)

    Grunder, A.; Moore, N. E.; Bohrson, W. A.

    2015-12-01

    The Steens Basalts (~16.7 Ma), the oldest and most mafic stage of Columbia River flood basalt volcanism, are known for lavas with conspicuous giant plagioclase laths (2 - 5 cm in diameter). Such flows are intercalated with ones that are nearly aphyric or that bear plagioclase (plag) phenocrysts of 0.5-2 cm. Addition textures are distinctive radial, snowflake plag clusters and sandwich glomerocrysts of plag, with olivine trapped between laths. These clusters and glomerocrysts are typically 1, but as large as 3 cm in diameter. Plag composition of all textural types is limited (An76-60). Plag dominates the phenocryst mode; rare flows, mainly low in the section, have olivine > plag and phenocrystic clinopyroxene occurs rarely, and mainly high in the section. Unlike the flows, dikes have few phenocrysts; giant laths are rare and the snowflake texture has not been observed. Giant plag laths are euhedral and make up a few percent to more than 50% of the rock. Many plag megacrysts are made of several plag crystals that form a mosaic, where the constituent crystals are crystallographically distinct and are overgrown with feldspar to make the crystal euhedral. We describe these composite megacrysts as "mosaicrysts". We are exploring magmatic conditions that would trigger oversaturation to spawn rapid growth yielding clusters and overgrowths that form mosaicrysts. Giant plagioclase basalts (so-called GPB) are also described for the Deccan and Emeishan flood basalt provinces attesting to similar magmatic processes. Plag laths typically define strong flow foliation at the flow base, have a swirled distribution in the flow core, and are sparse in the top. Some particularly crystal-rich flows (or sills) have an abrupt transition to a crystal-poor upper few decimeters of the several-m- thick flow. We interpret the crystal-poor top to be the expelled melt from crystal accumulation in the flow, which locally reinjects and is entrained in lower crystal mush.

  6. Petrogenesis of calcic plagioclase megacrysts in Archean rocks

    NASA Technical Reports Server (NTRS)

    Phinney, W. C.; Morrison, D. A.

    1986-01-01

    Anorthositic complexes with large equidimensional plagioclase grains of highly calcic composition occur in nearly all Archean cratons. Similar plagioclase occur as megacrysts in many Archean sills, dikes, and volcanic flows. In the Canadian Shield these units occur throughout the Archean portions of the entire shield and are particularly common as dikes over an area of a few 100,000 sq km in Ontario and Manitoba during a period of at least 100 m.y. in many different rock types and metamorphic grades. The plagioclase generally occurs in three modes: as inclusions in mafic intrusions at various stages of fractionation, as crystal segregations in anorthosite complexes, or as megacrysts in fractionated sills, dikes, and flows. Most occurrences suggest that the plagioclase was formed elsewhere before being transported to its present location. The evidence seems to be quite clear that occurrences of these types of calcic plagioclase require: (1) ponding of a relatively undifferentiated Archean tholeiitic melt at some depth; (2) isothermal crystallization of large, equidimensional homogeneous plagioclase crystals; (3) separation of the plagioclase crystals from any other crystalline phases; (4) further fractionation of melt; (5)transport of various combinations of individual plagioclase crystals and clusters of crystals by variously fractionated melts; and (6) emplacement as various types of igneous intrusions or flows.

  7. An example of trondhjemite genesis by means of alkali metasomatism: Rockford Granite, Alabama Appalachians

    NASA Astrophysics Data System (ADS)

    Drummond, Mark S.; Ragland, Paul C.; Wesolowski, David

    1986-03-01

    A model for trondhjemite genesis is proposed where granite is transformed to trondhjemite via infiltration by a Na-rich metamorphic fluid. The Rockford Granite of the Northern Alabama Piedmont serves as the case example for this process and is characterized as a synmetamorphic, peraluminous trondhjemite-granite suite. The major process operative in the conversion of granite to trondhjemite involves cation exchange of Na for K in the feldspar and mica phases through a volatile fluid medium. Whole-rock δ 18O values for the trondhjemites are negatively correlated with atomic proportion K/Na ratio indicating a partial reequilibration of the altered granitoids with a Na- and18O-rich metamorphically derived fluid. Biotite decomposition to an Al-epidote-paragonitic muscovite-secondary quartz assemblage is also associated with the sodium metasomatism, as are apatite replacement by Al-epidote and secondary zircon crystallization. Rare albitization of primary magmatic plagioclase and discontinuous grossularite reaction rim growth on magmatic garnet are present in the trondhjemites indicating the mobility of Ca during alkali metasomatism. The replacement of magmatic phases by me tasomatic phases exemplifies the chemical changes produced during infiltration metasomatism where the trondhjemites are depleted in P2O5, Th, Rb, U, K2O, V, Sn, F, MgO, Pb, TiO2, FeO* and Li and enriched in CaO, Na2O, Zr and Sr relative to the granites. Other elements, such as Cr, MnO, Cu, Zn, Co, Ba, SiO2, Ni, Al2O3, are shown to be relatively immobile during the metasomatism. The infiltration metasomatism probably occurred during prograde regional metamorphism, when a discrete fluid phase was produced in the surrounding amphibolite-grade metasediments. Foliation planes in the granite apparently served as conduits for fluid flow with reaction-enhanced permeability accompanying the 8% molar volume reduction during Na-for-K exchange in the feldspars. A source for the Na and Sr in the metamorphic fluid

  8. Multiple Feldspar replacement in Hercynian granites of the Montseny-Guilleries Massif (Catalan Coastal Ranges, NE Spain)

    NASA Astrophysics Data System (ADS)

    Fàbrega, Carles; Parcerisa, David; Gómez-Gras, David

    2013-04-01

    The core of the Montseny-Guilleries Massif (Catalan Coastal Ranges) is mainly composed by late-Hercynian granitoids (leucogranites and granodiorites) intruded within Cambrian to Carnoniferous metasediments. The granites are unconformably covered by Triassic (Buntsandstein) and Paleocene red beds at the western boundary, preserving a continuous outcrop of the Permo-Triassic unconformity for about 20 km. In the southwestern Montseny-Guilleries Massif the granites are covered by the Buntsandstein red sandstones that overlain a peneplain paleorelief called the Permo-Triassic palaeosurface. Beneath the palaeosurface the granite displays a characteristic pink colouration. This pink alteration is characterized by precipitation of minute heamatite crystals and albitization of pristine plagioclases (mostly labradorite). The secondary albite is pseudomorphic (mono- or polycrystalline), optically continuous, non-luminiscent, contains widespread microporosity and displays compositions about Ab98. These features are typical of low temperature replacive feldspars (Kastner and Siever, 1979). Albitization of plagioclases is almost total close to the Permo-Triassic palaeosurface and progressively decreases towards depth, displaying a 150-200 m thick alteration profile. The formation of this profile was controlled by fluid circulation along macro- and microfractures and crystal boundaries. Inside the plagioclase crystals fluid pathways were microfractures, twinning and cleavage planes and crystalline defects. The secondary albite holds widespread unconnected micron-size porosity often filled by Fe-oxides. The reaction front is sharp and displays an abrupt composicional change (Ab65 to Ab98) at micron scale. Porosity only appears to be connected at this reaction front surface. The geometrical arrangement of this alterations suggest that albitization was a shallow process related with Na-rich descending fluids linked to the Permo-Triassic palaeosurface, in a similar way to

  9. Element Transport in Granulite-Facies Fluids: a TEM Study in Exsolved Ternary Feldspar From Charnockites of Lofoten, Norway

    NASA Astrophysics Data System (ADS)

    Hartmann, K. T.; Wirth, R.; Markl, G.

    2006-12-01

    TEM was used to study exsolution features in feldspars indicative of high-p-T fluid transport during granulite facies metamorphism in charnockites from the Lofoten Islands in Northern Norway. The protoliths formed about 1750 Ma ago, at about ~800 to 900°C and 4 kbar. During a crustal thickening event, they reached high-pressure granulite-facies conditions of about 8-11 kbar at ~700°C (1). During this event, tiny magmatic pyroxenes enclosed in alkali feldspar reacted with a fluid to Cl-rich amphiboles and biotite. These have always a direct connection to elongated albite exsolutions which seem to surround amphiboles and biotite arranged in a linear fashion. This is evidence of extensive element transport (Fe, H, Cl) through the feldspar. The primary pyroxenes show no spatial relation to the lamellae and are evenly distributed in the feldspars. We tried to unravel the details of the transport and transformation mechanisms recorded by these textures using EMPA and TEM. Focused Ion Beam (FIB) prepared TEM-foils (2) revealed that pyroxenes, when spatially connected to albite exsolutions, show dissolution features. Additionally, amorphous Fe- and Cl-bearing material was found in albite lamellae even when not connected to a pyroxene. Based on composition, nanostructures and the known p-T-history, we propose the following succession of events. Feldspar containing small magmatic pyroxenes began to exsolve between about 800 and 650°C. The exsolution lamellae changed from coherent to incoherent and a fluid infiltrated the feldspar along nanotunnels (see also 3) at the margins of the exsolution lamellae. When the fluid had access to pyroxene, reaction took place and either amphibole or biotite formed. This study shows that fluid migration at elevated p and T is strongly dependent on the mineralogy of the percolated rocks. Exsolving alkali feldspars may offer fluid pathways not yet considered in studies on metamorphic fluid flow which is typically believed to happen along

  10. The Nature of Feldspar Clouding and Its Paleomagnetic Significance With Reference To The 2.45 Ga Matachewan Dyke Swarm, Canada

    NASA Astrophysics Data System (ADS)

    Halls, Henry C.; Zhang, Baoxing; Garland, Mary

    Clouding in calcic plagioclase is a common occurrence in Precambrian diabase dyke swarms worldwide, particularly those of Paleoproterozoic age. The occurrence of this clouding in 2.45 Ga Matachewan dykes within uplifted blocks of the Kapuskasing Zone (KZ) in Canada, and not in dykes of the same swarm at shallower crustal levels in surrounding terranes, suggests that the clouding is produced as a re- equilibration of the felspar in response to declining temperatures but in the presence of pressures appropriate to mid - to lower- crustal levels. We have made the following observations on feldspar separates extracted from the dykes: (1) Curie Balance, and low temperature SIRM acquisition studies show Curie temperarures of 580° C and a Verwey transition at 110-120K appropriate for Ti-poor magnetite; (2) Saturation magnetization is proportional to clouding intensity as determined from image analysis techniques; (3) Hysteresis and SEM studies indicate that the particles are small, typically about 1 micron (PSD) in size; (4) A baked contact test on cloudy feldspar dykes within the KZ is negative, but positive for dykes outside the KZ; (5) Magnetite in cloudy feldspars carries a high coercivity N component of magnetization which increases with clouding intensity, whereas dykes outside the KZ mostly carry an older R remanence; (6) Since sets of R dykes become N along strike on entering the KZ, the magnetization carried by cloudy feldspars is secondary; (7) The presence of R host rocks adjacent to an N cloudy dyke and the occasional survival of lower Hc and lower Tub R components in N cloudy dykes within the KZ suggests that the N magnetization of the feldspar magnetite is a CRM; (8) SEM shows that feldspars of different clouding intensity (from image analysis) have a near constant atomic percentage of Fe, so that the degree of clouding is determined in part by the concentration of magnetite rather than by total Fe and indicates that from 30-90% of the total Fe is used in

  11. Characterization and Thermodynamics Studies of Feldspar and Feldspathoid Minerals

    NASA Astrophysics Data System (ADS)

    Rudow, M.; Lilova, K.

    2015-12-01

    The application of thermal analysis and calorimetry for the studies of minerals has a history as long as the existence of the thermal methods themselves. New advanced calorimetric techniques have been developed for more accurate characterization of both bulk and nano materials thus impacting their design, processing, and applications. TG-DTA and TG-DSC are used to characterize the composition of complex minerals (e.g. [KxNa1-x(AlSi3)O8]) based on the weight changes and phase transformations observed with temperature increase. Additionally, those techniques allow to determine the quantity of the different types of water contained in natural feldspars and feldspathoids (absorbed, interlayer, structural). The results for several clays will be discussed. The geochemical properties and thermal stability of another class of minerals - aluminosilicate frameworks (alkali sodalities, natrolites, etc.) as related to high-level nuclear waste treatment facilities, radioactive waste storage and management were studied. The natural sodalite Na8[Al6Si6O24]Cl2 and similar frameworks with different anions are part of sodium-aluminosilicate (NAS) low activity radioactive waste produced during steam reforming process treatment. The enthalpies and entropies of formation and the hydration enthalpies of the above-mentioned feltspathoids are obtained and the effect of the different cations and anions on the thermodynamic stability was studied. The results will allow to predict the long term behavior of the compounds in the environment under different conditions.

  12. The surface chemistry of dissolving labradorite feldspar

    NASA Astrophysics Data System (ADS)

    Casey, William H.; Westrich, Henry R.; Arnold, George W.; banfield, Jillian F.

    1989-04-01

    Elastic recoil detection (ERD) analysis was used in conjunction with Rutherford backscattering (RBS) analysis to determine depth profiles of hydrogen, silicon, aluminum and calcium in labradorite crystals reacted under various pH conditions. The inventory of hydrogen in the mineral is strongly affected by solution pH. Hydrogen extensively infiltrates the mineral during reaction for 264 hours with solutions in the pH range 1-3. Infiltration is accompanied by extensive removal of sodium, calcium and aluminum from the mineral. This incongruent reaction proceeds to several hundreds of angstroms of depth and produces a silicon-rich surface which is amorphous to electron diffraction. The amount of hydrogen in the reacted layer is much less than is predicted from knowledge of the quantity of cations leached from the feldspar. These low inventories of hydrogen suggest that hydrogen-bearing groups in the reacted layer repolymermize subsequent to ion exchange and depolymerization reactions. This repolymerization eliminates hydrogen from the layer. At higher pH conditions (pH > 5), hydrogen inventories in the crystals decrease with time relative to an unreacted reference crystal. Hydrogen does not infiltrate beyond the first few unit cells of feldspar. Thus, dissolution in slightly acid, near-neutral, and basic solutions proceeds at the immediate surface of the feldspar. Within the limit of the RBS technique, there is no evidence for incongruent dissolution at these conditions.

  13. Plagioclase-rich inclusions in carbonaceous chondrite meteorites - Liquid condensates?

    NASA Technical Reports Server (NTRS)

    Wark, D. A.

    1987-01-01

    The characteristics and formation of coarse-grained, plagioclase-rich inclusions are investigated. The textures, mineralogical compositions, and initial Al-26/Al-27 ratios for the plagioclase-rich inclusions are described. It is observed that plagioclase-rich inclusions in carbonaceous chondrites are either Ca-Al-rich inclusions (CAIs) composed of 30-60 vol pct anorthite, and less than 35 vol pct Ti-Al-pyroxene and melilite, or CA chondrites composed of plagioclase, pyroxene, olivine, spinel, and melilite. It is observed that CA chondrules are chemically and mineralogically the most similar components shared by carbonaceous and ordinary chondrites. The textural changes observed in the inclusions are examined. The data reveal that the CAIs have three textural groups: coarse anorthite laths, equigranular anorthite and Ti-Al-pyroxene, and lacy Ti-Al-pyroxene and fine-grained anorthite.

  14. Sintering behaviour of feldspar and influence of electric charge effects

    NASA Astrophysics Data System (ADS)

    Gallala, W.; Gaied, M. E.

    2011-04-01

    The characterization of feldspar for electric porcelain and the behaviour of these materials after heating at 1230°C were studied. X-ray diffraction (XRD) and scanning electronic microscopy (SEM) were used to identify the present phases and the densification level. Feldspar sand was treated by flotation. The floated feldspar is constituted by microcline, quartz, and minor amounts of albite. The microstructure of sintered feldspar at 1230°C is essentially vitreous with open microporosities. The dielectrical properties of composites were characterized by using the induced courant method (ICM), which indicates that the charge trapping capacity depends on the mineralogical and chemical composition of feldspar.

  15. Deformation behaviour of feldspar in greenschist facies granitoide shear zones from the Austroalpine basement to the south of the western Tauern window, Eastern Alps

    NASA Astrophysics Data System (ADS)

    Hentschel, Felix; Trepmann, Claudia

    2015-04-01

    Objective of this study is to elucidate the feldspar deformation behaviour at greenschist facies conditions relevant for the long-term rheological properties of continental crust. Uncertainties in models for the rheological properties are partly due to a poor knowledge of the deformation mechanisms taking place in granitoid rocks at inaccessible depth. The deformation behaviour of feldspar, the most abundant mineral in the continental crust, is characterized by an interaction of brittle, dissolution-precipitation and crystal-plastic processes, which is difficult to evaluate in experiments given the problematic extrapolation of experimental conditions to reasonable natural conditions. However, microfabrics of metamorphic granitoid rocks record the grain-scale deformation mechanisms and involved chemical reactions proceeding during their geological history. This usually includes deformation and modification through several stages in space (depth, i.e., P, T conditions) and/or time. For deciphering the rock's record this implies both, challenge and chance to resolve these different stages. Here, we use the deformation record of mylonitic pegmatites from the Austroalpine basement south to the western Tauern window. The structural, crystallographic and chemical characteristics of the feldspar microfabrics are determined via micro-analytical techniques (polarized light microscopy, scanning electron microscopy, SEM, electron back scatter diffraction, EBSD) to identify the relevant deformation mechanisms and deformation conditions. The pegmatites represent a relatively simple Ca-poor granitoid system, mineralogically dominated by albite-rich plagioclase, K-feldspar and quartz. The matrix of the mylonitic pegmatites is composed of alternating monomineralic albite and quartz ribbons defining the foliation. Fragmented tourmaline and K-feldspar porphyroclasts occur isolated within the matrix. At sites of dilation along the stretching lineation K-feldspar porphyroclasts show

  16. Linking Deformation and Diffusion to Develop a Strain Speedometer in Plagioclase

    NASA Astrophysics Data System (ADS)

    Barshi, N.; Rowe, C. D.; van Hinsberg, V.

    2015-12-01

    Microscopic mobility of atoms in minerals controls macroscopic metamorphic and tectonic processes in Earth's crust. Deformation and diffusion, each an expression of this mobility, are both processes of breaking and reforming bonds and take energy to proceed. Deformation can facilitate diffusion by supplying strain energy that facilitates breaking bonds and enhance diffusion rates by mobilizing dislocations, which localize atomic migration. Deformation-enhanced diffusion may therefore lower closure temperatures for geochronometers and thermobarometers. If the effect of deformation on diffusion is measurable, we must reevaluate these tools for deformed rocks. We explore this effect and its potential as the basis for estimating duration and rate of strain in the rock record. We focus on feldspar, a rheologically and modally dominant mineral in Earth's crust for which deformation and diffusion parameters are well known. Different elements have different diffusion rates within each mineral, which are differentially accelerated by a deformation-induced reduction of their activation energies for diffusion. We present the first comprehensive study of strain enhancement of diffusion in plagioclase, a combination of km-scale, thin-section-scale, and grain-scale strain and chemical measurements for major and trace elements in naturally deformed plagioclase phenocrysts from the San José Pluton, Peninsular Ranges Batholith, México. Our samples had low initial compositional contrasts and experienced low strain. Under these conditions, the effect of strain-enhanced element mobility, as predicted from our model, is below analytical detection limits. For these rocks, a static diffusion model is sufficient, and thermobarometers and geochronometers can still be applied to yield accurate results.

  17. Energy related studies utilizing K-feldspar thermochronology. Progress performance report, 1990--1993

    SciTech Connect

    Not Available

    1993-05-01

    Two distinct sources of information are available from a {sup 40}Ar/{sup 39}Ar step-heating experiment: the age spectrum and Arrhenius plot. Model ages are calculated from the flux of radiogenic argon ({sup 40}Ar*) (assuming trapped argon of atmospheric composition) relative to the reactor produced {sup 39}Ar evolved during discrete laboratory heating steps. With the additional assumption that the {sup 39}Ar is uniformly distributed within the sample, we can infer the spatial distribution of the daughter product. ne associated Arrhenius plot, derived by plotting the diffusion coefficient (obtained from the inversion of the 39{sup Ar} release function assuming a single domain) against the inverse temperature of laboratory heating, are a convolution of the parameters which characterize the individual diffusion domains (whether these be dictated by varying length scale, energetics, etc.). However, many and perhaps Most {sup 40}Ar/{sup 39}Ar age spectra for slowly cooled alkali feldspars are significantly different from model age spectra calculated assuming a single diffusion-domain size. In addition, Arrhenius plots calculated from the measured loss of {sup 39}Ar during the step heating experiment show departures from linearity that are inconsistent with diffusion from domains of equal size. By extending the single diffusion-domain closure model (Dodsontype) to apply to minerals with a discrete distribution of domain sizes, we obtained an internally consistent explanation for the commonly observed features of alkali feldspar age spectra and their associated Arrhenius plots.

  18. Distribution and textures of K-feldspar grains in the George Ashley Block layered-aplite pegmatite intrusive

    NASA Astrophysics Data System (ADS)

    Kleck, W. D.

    2013-12-01

    Both Johns & Tuttle (1963) and London (2008) note that the distribution of potassium is neither uniform nor symmetrical in some pegmatite bodies. A detailed chemical and mineral analysis of the George Ashley Block (Kleck & Foord 1999) shows that the distribution of K-feldspar over the entire body is generally uniform, but not symmetrical. The amounts of quartz, plagioclase, muscovite, and garnet are neither uniform nor symmetrical. It is noted that layered-aplite, pegmatite intrusives (terminology of Jahns & Tuttle 1963) are intruded horizontally, and it is suggested that these are the pegmatite bodies which have this non-uniform distribution of minerals. These types of pegmatite bodies are distinctly different from other pegmatite bodies in several ways. The core zone in these bodies is not centrally located and typically divides these bodies into a pegmatitic top and an aplitic bottom; the top and bottom appear to be contemporaneous. The features and content of the border- and core-zones are not included in this discussion. The texture of the K-feldspar in the top of these bodies is generally pegmatitic; some of the K-feldspar grains may exist as ultra-large grains which have a teardrop shape or minor-crystal surfaces. In the bottom of these bodies, the K-feldspar is commonly rounded grains approximately 1 mm in diameter; rarely, some K-feldspar grains here are centimeter-grained with crystal surfaces indicating growth. In the George Ashley Block, the concentration and distribution of K-feldspar is inversely symmetrical in the top vs. bottom. In the top it increases toward the core zone; K-feldspar--20 increasing to 60 vol% (all values one significant figure) and K2O--3 increasing to 8 wt%. In the bottom it decreases toward the core zone; K-feldspar--40 decreasing to 0 vol% and K2O--4 decreasing to 0 wt%. The two trends are approximately parallel and the total amounts are approximately constant. The suggested conditions and mechanisms (with the added condition of

  19. Igneous phenocrystic origin of K-feldspar megacrysts in granitic rocks from the Sierra Nevada batholith

    USGS Publications Warehouse

    Moore, J.G.; Sisson, T.W.

    2008-01-01

    Study of four K-feldspar megacrystic granitic plutons and related dikes in the Sierra Nevada composite batholith indicates that the megacrysts are phenocrysts that grew in contact with granitic melt. Growth to megacrystic sizes was due to repeated replenishment of the magma bodies by fresh granitic melt that maintained temperatures above the solidus for extended time periods and that provided components necessary for K-feldspar growth. These intrusions cooled 89-83 Ma, are the youngest in the range, and represent the culminating magmatic phase of the Sierra Nevada batholith. They are the granodiorite of Topaz Lake, the Cathedral Peak Granodiorite, the Mono Creek Granite, the Whitney Granodiorite, the Johnson Granite Porphyry, and the Golden Bear Dike. Megacrysts in these igneous bodies attain 4-10 cm in length. All have sawtooth oscillatory zoning marked by varying concentration of BaO ranging generally from 3.5 to 0.5 wt%. Some of the more pronounced zones begin with resorption and channeling of the underlying zone. Layers of mineral inclusions, principally plagioclase, but also biotite, quartz, hornblende, titanite, and accessory minerals, are parallel to the BaO-delineated zones, are sorted by size along the boundaries, and have their long axes preferentially aligned parallel to the boundaries. These features indicate that the K-feldspar megacrysts grew while surrounded by melt, allowing the inclusion minerals to periodically attach themselves to the faces of the growing crystals. The temperature of growth of titanite included within the K-feldspar megacrysts is estimated by use of a Zr-in-titanite geothermometer. Megacryst-hosted titanite grains all yield temperatures typical of felsic magmas, mainly 735-760 ??C. Titanite grains in the granodiorite hosts marginal to the megacrysts range to lower growth temperatures, in some instances into the subsolidus. The limited range and igneous values of growth temperatures for megacryst-hosted titanite grains support the

  20. Plagioclase deformation in upper-greenschist facies meta-pegmatite mylonites from the Austroalpine Matsch Unit (Eastern Alps, Italy)

    NASA Astrophysics Data System (ADS)

    Eberlei, Tobias; Habler, Gerlinde; Abart, Rainer; Grasemann, Bernhard

    2014-05-01

    Feldspars are common rock forming minerals as they are stable over a wide range of bulk rock compositions and metamorphic conditions within the Earth's crust. The deformation mechanisms of feldspar play an important role in rheological models for the crust and therefore have received considerable attention in studies on natural rocks and in experimental studies. The interaction of frictional and viscous deformation mechanisms and the onset of crystal plastic deformation in feldspars occur over a broad range of pressures and temperatures. In this work, we present new microstructural, textural and mineral chemical data of plagioclase from Permian metapegmatites within the Austroalpine Matsch Unit in Southern Tyrol (Italy). These crystalline basement rocks were deformed and metamorphosed at conditions close to the greenschist/amphibolites facies transition at 480±26°C during the Cretaceous (Habler et al., 2009). The investigated samples have been collected from meter-scale shear zones which typically occur at boundaries of lithological subunits. The southern tectonic boundary of this unit is commonly referred to as the "Vinschgau Shear Zone" (Schmid & Haas, 1989). We applied the Electron Backscatter Diffraction method to investigate the grain- and subgrain-boundaries and the nature of effective deformation mechanisms in plagioclase. Large albite porphyroclasts in the mylonitic Permian metapegmatites show grain internal traces of dissolution surfaces and the formation of new, strain-free grains with straight grain boundary segments and partly 120° grain boundary triple junctions in dilatant sites. The aggregates of new grains neither have a lattice preferred orientation nor a crystallographic orientation relation with the adjacent clast, and are characterized by the lack of grain internal deformation, suggesting that these are new precipitates rather than clast-fragments or recrystallized subgrains. Furthermore, the porphyroclasts show cracks and kinks, associated

  1. Linking Plagioclase Zoning Patterns to Active Magma Processes

    NASA Astrophysics Data System (ADS)

    Izbekov, P. E.; Nicolaysen, K. P.; Neill, O. K.; Shcherbakov, V.; Plechov, P.; Eichelberger, J. C.

    2015-12-01

    Plagioclase, one of the most common and abundant mineral phases in volcanic products, will vary in composition in response to changes in temperature, pressure, composition of the ambient silicate melt, and melt H2O concentration. Changes in these parameters may cause dissolution or growth of plagioclase crystals, forming characteristic textural and compositional variations (zoning patterns), the complete core-to-rim sequence of which describes events experienced by an individual crystal from its nucleation to the last moments of its growth. Plagioclase crystals in a typical volcanic rock may look drastically dissimilar despite their spatial proximity and the fact that they have erupted together. Although they shared last moments of their growth during magma ascent and eruption, their prior experiences could be very different, as plagioclase crystals often come from different domains of the same magma system. Distinguishing similar zoning patterns, correlating them across the entire population of plagioclase crystals, and linking these patterns to specific perturbations in the magmatic system may provide additional perspective on the variety, extent, and timing of magma processes at active volcanic systems. Examples of magma processes, which may be distinguished based on plagioclase zoning patterns, include (1) cooling due to heat loss, (2) heating and/or pressure build up due to an input of new magmatic material, (3) pressure drop in response to magma system depressurization, and (4) crystal transfer between different magma domains/bodies. This review will include contrasting examples of zoning patters from recent eruptions of Karymsky, Bezymianny, and Tolbachik Volcanoes in Kamchatka, Augustine and Cleveland Volcanoes in Alaska, as well as from the drilling into an active magma body at Krafla, Iceland.

  2. The origin of olivine-rich troctolites/plagioclase-dunites

    NASA Astrophysics Data System (ADS)

    Garapic, G.; Faul, U.; Kruckenberg, S. C.; Wiejaczka, J.; Newton, J. C.

    2015-12-01

    Olivine-rich troctolites or plagioclase dunites are a type of rock commonly found in oceanic crust and peridotite massifs that does not fit into a IUGS classification. Part of the reason is that their origin is poorly constrained, in particular whether these rocks are cumulates or residual mantle rocks. To avoid implications for origin or process Blackman et al. 2006 defined as olivine-rich troctolites rocks that contain > 70% olivine,with plagioclase, cpx and spinel. We examined this type of rock in Krivaja peridotite massif in Bosnia-Herzegovina where it occurs as massive outcrops with an area of several tens of square kilometres. The plagioclase dunites are underlain by peridotites that contain plagioclase patches indicative of melt migration. These peridotites are progressively depleted of pyroxene and cross-cut by gabbro veins. The plagioclase dunites have Mg# predominantly from 89 - 90 and Ni contents from 2500 - 3500 ppm, similar to the peridotites. EBSD mapping of whole thin sections shows orientation distribution functions (odf) that are unlike any of the fabric types observed in naturally or experimentally deformed rocks with a strong maximum in (001) near the foliation plane (although this plane is poorly defined) and weak girdles of the other two axes perpendicular to it. For comparison, we also mapped known cumulates from the Rum and Stillwater layered intrusions with somewhat lower Mg# of 84 - 86. The odf of these samples show a strong maximum of (010) perpendicular to the foliation plane and weak girdles of the other two axes in the plane. This fabric type has been explained by crystal settling and compaction in a magma chamber. Together these observations show that the plagioclase dunites from Krivaja, as well as rocks with similar characteristics e.g. from the Mid-Atlantic Ridge (Drouin et al. 2010) and Italy (Renna and Tribuzio, 2011) are not cumulates but are of mantle origin. An important characteristic of the plagioclase dunites is that the

  3. Shocked plagioclase signatures in Thermal Emission Spectrometer data of Mars

    USGS Publications Warehouse

    Johnson, J. R.; Staid, M.I.; Titus, T.N.; Becker, K.

    2006-01-01

    The extensive impact cratering record on Mars combined with evidence from SNC meteorites suggests that a significant fraction of the surface is composed of materials subjected to variable shock pressures. Pressure-induced structural changes in minerals during high-pressure shock events alter their thermal infrared spectral emission features, particularly for feldspars, in a predictable fashion. To understand the degree to which the distribution and magnitude of shock effects influence martian surface mineralogy, we used standard spectral mineral libraries supplemented by laboratory spectra of experimentally shocked bytownite feldspar [Johnson, J.R., Ho??rz, F., Christensen, P., Lucey, P.G., 2002b. J. Geophys. Res. 107 (E10), doi:10.1029/2001JE001517] to deconvolve Thermal Emission Spectrometer (TES) data from six relatively large (>50 km) impact craters on Mars. We used both TES orbital data and TES mosaics (emission phase function sequences) to study local and regional areas near the craters, and compared the differences between models using single TES detector data and 3 ?? 2 detector-averaged data. Inclusion of shocked feldspar spectra in the deconvolution models consistently improved the rms errors compared to models in which the spectra were not used, and resulted in modeled shocked feldspar abundances of >15% in some regions. However, the magnitudes of model rms error improvements were within the noise equivalent rms errors for the TES instrument [Hamilton V., personal communication]. This suggests that while shocked feldspars may be a component of the regions studied, their presence cannot be conclusively demonstrated in the TES data analyzed here. If the distributions of shocked feldspars suggested by the models are real, the lack of spatial correlation to crater materials may reflect extensive aeolian mixing of martian regolith materials composed of variably shocked impact ejecta from both local and distant sources. ?? 2005 Elsevier Inc. All rights

  4. Synthesis for Lunar Simulants: Glass, Agglutinate, Plagioclase, Breccia

    NASA Technical Reports Server (NTRS)

    Weinstein, Michael; Wilson, Stephen A.; Rickman, Douglas L.; Stoeser, Douglas

    2012-01-01

    The video describes a process for making glass for lunar regolith simulants that was developed from a patented glass-producing technology. Glass composition can be matched to simulant design and specification. Production of glass, pseudo agglutinates, plagioclase, and breccias is demonstrated. The system is capable of producing hundreds of kilograms of high quality glass and simulants per day.

  5. Contrasting Sr isotope ratios in plagioclase from different formations of the mid-Miocene Columbia River Basalt Group

    NASA Astrophysics Data System (ADS)

    Starkel, W. A.; Wolff, J.; Eckberg, A.; Ramos, F.

    2008-12-01

    Many early Columbia River Basalt flows of the Steens and Imnaha Formations are characterized by abundant, texturally complex, coarse plagioclase phenocrysts. In Imnaha lavas, the feldspars typically have more radiogenic 87Sr/86Sr than whole rock and matrix, and may exhibit complex isotopic zoning that is not correlated with An content. Imnaha plagioclase grains are interpreted as variably-contaminated crystals produced when high-crystallinity mid-crustal basaltic intrusions exchanged interstitial melt with adjacent partly-melted crustal rock; this isotopically variable debris was then remobilized by subsequent intrusion of mantle-derived basalt and brought to the surface as an isotopically heterogeneous mixture. In contrast, plagioclase grains in the texturally very similar Steens lavas are isotopically near-homogeneous and 87Sr/86Sr is not significantly displaced from that of the bulk rock. This is consistent with magma- crust interaction at low degrees of crustal melting during the early stages of the Columbia River flood basalt episode, where Steens and Imnaha lavas were erupted from distinct magma systems hosted by different types of crust that exerted different degrees of isotopic leverage on the mantle-derived magmas [1]. Thermal input to the Steens system declined at the same time as the Imnaha magmatic flux increased to ultimately produce the huge outpouring of Grande Ronde lavas, which are mixtures of mantle- and crust-derived liquids, the latter produced during high degrees of crustal melting during the time of peak magmatic flux. [1] Wolff et al. (2008) Nature Geoscience 1, 177-180.

  6. Alkali metal nitrate purification

    DOEpatents

    Fiorucci, Louis C.; Morgan, Michael J.

    1986-02-04

    A process is disclosed for removing contaminants from impure alkali metal nitrates containing them. The process comprises heating the impure alkali metal nitrates in solution form or molten form at a temperature and for a time sufficient to effect precipitation of solid impurities and separating the solid impurities from the resulting purified alkali metal nitrates. The resulting purified alkali metal nitrates in solution form may be heated to evaporate water therefrom to produce purified molten alkali metal nitrates suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of purified alkali metal nitrates.

  7. A Record of Magmatic Water Content Preserved in Hydroxyl Concentrations of Plagioclase Phenocrysts From the 1980-1981 Eruption Sequence of Mount St. Helens

    NASA Astrophysics Data System (ADS)

    Johnson, E. A.

    2004-12-01

    Volatiles, and particularly water, influence many of the properties of volcanic systems including melt viscosity and crystallinity, and the explosive or effusive nature of an eruption. Magmatic water content could potentially be determined by measurement of OH concentrations in phenocrysts, assuming an equilibrium partitioning of water between the phenocrysts and melt. The concentration of OH in volcanic feldspars may also reflect many factors other than magmatic water content, including melt composition, oxygen fugacity, and thermal history. In this study, the OH concentrations of plagioclase phenocryts from four eruptions of Mount St. Helens between May 18, 1980 and April 1981 were measured using infrared spectroscopy in order to evaluate this method of determining magmatic water content. The eruption temperature, oxygen fugacity, and bulk chemical composition were all fairly constant through the eruption sequence from 1980-1981 at Mount St. Helens. The water content of melts from successive eruptions decreased from 4.6 wt% H2O for the Plinian eruption on May 18, 1980 (Rutherford et al. 1985, JGR 90, 2929-2947), to less than 1 wt% H2O for the latest dome-forming dacites. Plagioclase from the pumice erupted during the May 18, 1980 event contains 200 ppm H2O by weight as structural hydroxyl groups, whereas feldspars from subsequent explosive eruptions with melt water concentrations about half that of the May 18 eruption (Melson 1983, Science 221, 1387-1391) contain about half the structural OH content (about 110 ppm for the October 16, 1980 and August 7, 1980 eruptions). The effusive dome-building eruption of April 1981 contains plagioclase with very low (about 20 ppm) water content, implying possible diffusive loss of hydrogen during the prolonged period of eruption. Homogeneous distribution of OH in feldspar grains > 100 micrometers is observed even for those grains with pronounced major element zoning. These data show that, in the absence of changes in oxygen

  8. Lunar granites with unique ternary feldspars

    NASA Technical Reports Server (NTRS)

    Ryder, G.; Stoeser, D. B.; Marvin, U. B.; Bower, J. F.

    1975-01-01

    An unusually high concentration of granitic fragments, with textures ranging from holocrystalline to glassy, occurs throughout Boulder 1, a complex breccia of highland rocks from Apollo 17, Station 2. Among the minerals included in the granites are enigmatic K-Ca-rich feldspars that fall in the forbidden region of the ternary diagram. The great variability in chemistry and texture is probably the result of impact degradation and melting of a granitic source-rock. Studies of the breccia matrix suggest that this original granitic source-rock may have contained more pyroxenes and phosphates than most of the present clasts contain. Petrographic observations on Apollo 15 KREEP basalts indicate that granitic liquids may be produced by differentiation without immiscibility, and the association of the granites with KREEP-rich fragments in the boulder suggests that the granites represent a residual liquid from the plutonic fractional crystallization of a KREEP-rich magma. Boulder 1 is unique among Apollo 17 samples in its silica-KREEP-rich composition. We conclude that the boulder represents a source-rock unlike the bedrock of South Massif.

  9. Plagioclase-melt equilibria. [crystallization from magmatic liquid

    NASA Technical Reports Server (NTRS)

    Drake, M. J.

    1976-01-01

    Results of experiments investigating the crystallization of plagioclase from natural and synthetic melts are presented and are analyzed in terms of empirical and semiquantitative mixing models for the melt. Elemental partition constants were determined from the results and from other published data. Activities of the melt components were modeled by assuming that the melt consists of two independent quasi-lattices of network-forming and network-modifying components, each of which is an ideal solution of its respective component. The semiquantitative analysis supports the suggestion that Na(+) is strongly associated with tetrahedrally-coordinated Al in the melt. It is shown that it is possible to predict the composition of plagioclase crystallizing under equilibrium conditions from a dry melt of known composition and known temperature at low total pressure.

  10. Skaergaard Liquidus Temperatures and the Frailty of Plagioclase Thermometry

    NASA Astrophysics Data System (ADS)

    Morse, S. A.

    2010-12-01

    Because of its refractory nature and low diffusivity, plagioclase is the only mineral likely to record liquidus temperatures of mafic magmas. As such, it has become a talisman of such thermometry, but with limited success. Precise thermal information can perhaps best be obtained experimentally by finding the unique cotectic assemblage of all relevant mineral compositions with melt at relevant pressure. By repeating such experiments at more evolved compositions a relevant plagioclase thermometric history should be obtained. This principle of cotectic calibration was that used as a starting point by Morse (2008). By contrast, unfiltered literature results of experimental plagioclase - liquid determinations were used by Thy et al. (2009), with a T-X regression through all the data including evolved compositions, to describe the Skaergaard liquidus. Implicit in this exercise was the hypothesis that all the data represented stable equilibria and that low-melting components at static melting behaved the same as if in fractional crystallization. Tests for stable equilibrium in such a database [including that of Putirka (2005) and many others as e.g. in LEPR (lepr.ofm-research.org)] can usefully start with an examination of plagioclase loop width versus temperature or plagioclase composition. The loop width of a binary solution against either T or X is described by a slightly skewed parabola anchored at zero at both ends and rising to a broad maximum near An60 in the case of plagioclase. The peak width in XAn (Sol - Liq) has a value of 0.32 at 1 atm in Di-An-Ab and 0.24 at An-57 in a MORB fractional crystallization exercise. Values falling outside this range downward are likely to reflect metastable compositions. All of the 54 data points in one source used by Thy et al. (2009) fall below this range and are scattered to as low as 0.04. Such a shotgun scatter defines metastability and the loss of calibration. Moderate scatter at much higher values of loop width in the LEPR

  11. Ice crystals growing on K-feldspar (microcline) have preferential orientation dictated by feldspar lattice structure

    NASA Astrophysics Data System (ADS)

    Kiselev, A. A.; Bachmann, F.; Pedevilla, P.; Cox, S.; Michaelides, A.

    2014-12-01

    Recently, we have conducted experiments on deposition nucleation and growth of ice on freshly cleaved natural K-feldspar (microcline) crystals exposed to water vapor in the Environmental Scanning Electron Microscope (ESEM, FEI Quanta 650 FEG). Independently adjusting the partial water vapor pressure in the sample chamber and the temperature of the substrate mounted on top of the double-stage Peltier element, deposition ice nucleation, growth, and sublimation can be studied within the temperature range from -5°C to -60°C. By using small crystal size and tilted geometry we have been able to record the video sequences of ice nucleation taking place on both 001 and 010 crystallographic planes simultaneously. Here, we report the following general features of ice nucleation and growth observed in these experiments: Nucleation of ice always starts before the water saturation is reached. Ice was preferentially nucleating on surface defects (steps, cracks, and pits) or on the debris particles scattered over the surface of feldspar crystal. Ice crystals grown via deposition at temperatures above -30°C on any of the feldspar crystal faces have shown the same directional and rotational orientation, with c-axis of ice aligned with the c-axis of microcline unit cell. Below -35°C no preferential orientation has been observed whatsoever. The majority of observed ice crystals exhibit the evaporation groove at the waist of hexagonal prism, indicting the presence of lattice dislocations in the crystal nucleation plane. We discuss a possible mechanism of crystal lattice alignment by considering layer of ordered water on the surface of feldspar crystal forming prior to ice nucleation. Using density functional theory we show how the mineral surface interacts with water, particularly addressing the interaction of surface cations and hydroxyl groups with a water overlayer. We argue that the misalignment of the 001 lattice planes for microcline and ice (inherently following from the

  12. Shocked Feldspar in L Chondrites: Deformation, Transformation and Local Melting

    NASA Astrophysics Data System (ADS)

    Fudge, C.; Sharp, T. G.

    2016-08-01

    We present textures and compositional profiles of partially to completely transformed plagioclase to maskelynite. Evidence for transformation mechanisms, including solid state transformation and crystallization from melt will be discussed.

  13. Grain-Recycling Zoning of Plagioclase and Metamorphic Fractionation

    NASA Astrophysics Data System (ADS)

    Pearce, M. A.; Wheeler, J.

    2008-12-01

    Quartzo-feldspathic gneisses make up much of the continental crust often having enjoyed a complex thermal history. Determining peak metamorphic conditions using conventional equilibrium thermodynamics is difficult because there are too many degrees of freedom. Zoned minerals are problematic, because of uncertainties in the exact equilibrium assemblage at any particular time, but provide a time-dependent measure of changes in equilibrium conditions. Zoning can arise due to diffusion of atoms into a homogeneous lattice from grain boundarys or through mineral growth under changing pressure, temperature or bulk rock composition. Conventional growth zoning considers a porphyroblast (commonly garnet) growing in an effectively homogeneous matrix with the growth rate controlled by reactions that produce new porphyroblast material. However, simulations of zoning developed by grain growth in a monophase domains of more complex rocks show boundary migration rates control the zoning geometry as shrinking grains are cannibalised by growing grains. This new grain-recycling zoning develops because chemical reactions change the composition of the material that is swept by the grain boundary without changing the mineral. A model of this process has been created using the Gibbs free energy minimisation software Theriak-Domino controlled by our custom written Matlab control program. This program assumes an initially homogeneous composition of equigranular plagioclase then uses the experimentally determined normal growth law for plagioclase to calculate the grain-size increase for a given time-step thus giving the amount of material swept. Assuming this is all available for reaction at the same time, the rest of the plagioclase is removed from the bulk composition, the equilibrium plagioclase composition calculated, and added to the growing grain. This fractionation alters the range of plagioclase compositions available over a given temperature range, changing PT estimates obtained

  14. APPLICATIONS OF CATHODOLUMINESCENCE OF QUARTZ AND FELDSPAR TO SEDIMENTARY PETROLOGY.

    USGS Publications Warehouse

    Ruppert, Leslie F.

    1987-01-01

    Cathodoluminescence (CL), the emission of visible light during electron bombardment, was first used in sandstone petrology in the mid-1960's. CL techniques are especially useful for determining the origin and source of quartz and feldspar, two of the most common constituents in clastic rocks. CL properties of both minerals are dependent on their temperature of crystallization, duration of cooling, and/or history of deformation. Detrital quartz and feldspar are typically derived from igneous and metamorphic sources and luminesce in the visible range whereas authigenic quartz and feldspar form at low temperatures and do not luminesce. Quantification of luminescent and non-luminescent quartz and feldspar with the scanning electron microscope, electron microprobe, or a commercial CL device can allow for the determination of origin, diagenesis, and source of clastic rocks when used in conjunction with field and other petrographic analyses.

  15. Investigation of Potassium Feldspar Reactivity in Wet Supercritical CO2 by In Situ Infrared Spectroscopy

    NASA Astrophysics Data System (ADS)

    Thompson, C.; Widener, C.; Schaef, T.; Loring, J.; McGrail, B. P.

    2014-12-01

    Capture and subsequent storage of CO2 in deep geologic reservoirs is progressively being considered as a viable approach to reduce anthropogenic greenhouse gas emissions. In the long term, injected CO2 may become permanently entrapped as silicate minerals react with CO2 enriched fluids to form stable carbonate minerals. Potassium feldspars are highly abundant in the earth's crust and are present in the caprocks and storage formations of many target reservoirs. While the dissolution kinetics and carbonation reactions of feldspars have been well studied in the aqueous phase, comparatively little work has focused on K-feldspar reactivity in the CO2-rich fluid. In this study, we used in situ infrared spectroscopy to investigate the carbonation reactions of natural microcline samples. Experiments were carried out at 50 °C and 91 bar by circulating dry or wet supercritical CO2 (scCO2) past a thin film of powdered sample. Water concentrations ranged from 0% to 125% relative to saturation, and transmission-mode absorbance spectra were recorded as a function of time for 48 hours. No discernible reaction was detected when the samples were exposed to anhydrous scCO2. However, in fully water-saturated scCO2, a thin film of liquid-like water was observed on the samples' surfaces, and up to 0.6% of the microcline was converted to a carbonate phase. Potassium carbonate is the most likely reaction product, but minor amounts of sodium carbonate and siderite may also have formed from minor sample impurities. The extent of reaction appears to be related to the thickness of the water film and is likely a consequence of the film's ability to solvate and transport ions in the vicinity of the mineral surface. Other features observed in the spectra correspond to microcline dissolution and precipitation of amorphous silica. Implications about the role of water in these reactions and the relative effectiveness of alkali feldspars for mineral trapping of CO2 will be discussed.

  16. In situ 40K-40Ca ‘double-plus’ SIMS dating resolves Klokken feldspar 40K-40Ar paradox

    NASA Astrophysics Data System (ADS)

    Harrison, T. Mark; Heizler, Matthew T.; McKeegan, Kevin D.; Schmitt, Axel K.

    2010-11-01

    The 40K- 40Ca decay system has not been widely utilized as a geochronometer because quantification of radiogenic daughter is difficult except in old, extremely high K/Ca domains. Even these environments have not heretofore been exploited by ion microprobe analysis due to the very high mass resolving power (MRP) of 25,000 required to separate 40K + from 40Ca +. We introduce a method that utilizes doubly-charged K and Ca species which permits isotopic measurements to be made at relatively low MRP (~ 5000). We used this K-Ca 'double-plus' approach to address an enduring controversy in 40Ar/ 39Ar thermochronology revolving around exsolved alkali feldspars from the 1166 Ma Klokken syenite (southern Greenland). Ion microprobe 40K- 40Ca analysis of Klokken samples reveal both isochron and pseudoisochron behaviors that reflect episodic isotopic and chemical exchange of coarsely exsolved perthites and a near end-member K-feldspar until ≤ 719 Ma, and perhaps as late at ~ 400 Ma. Feldspar microtextures in the Klokken syenite evolved over a protracted interval by non-thermal processes (fluid-assisted recrystallization) and thus this sample makes a poor model from which to address the general validity of 40Ar/ 39Ar thermochronological methodologies.

  17. Shishaldin volcano: Aleutian high-alumina basalts and the question of plagioclase accumulation

    SciTech Connect

    Fournelle, J.; Marsh, B.D. )

    1991-03-01

    High-alumina basalts (HABs) from volcanic arcs commonly contain 30%-50% (modal) plagioclase. It has been suggested that they reflect plagioclase addition and are not primary compositions. In rocks from the Aleutian volcano Shishaldin, the authors search for evidence of plagioclase accumulation: Al{sub 2}O{sub 3}, CaO, and Na{sub 2}O vs. modal plagioclase; europium anomalies in HABs; plagioclase-liquid equilibrium; and the HAB groundmass. The HABs do not appear to be results of plagioclase addition to liquids of dacitic, Fe-Ti enriched, or high-Mg basaltic compositions. Plagioclase loss from HABs does appear to yield the Fe-Ti-enriched basalts. Shishaldin HABs may reflect near-primary compositions, and HAB phase equilibria may thus be useful in evaluating the origin of such arc basalts.

  18. Brittle grain-size reduction of feldspar, phase mixing and strain localization in granitoids at mid-crustal conditions (Pernambuco shear zone, NE Brazil)

    NASA Astrophysics Data System (ADS)

    Viegas, Gustavo; Menegon, Luca; Archanjo, Carlos

    2016-03-01

    The Pernambuco shear zone (northeastern Brazil) is a large-scale strike-slip fault that, in its eastern segment, deforms granitoids at mid-crustal conditions. Initially coarse-grained (> 50 µm) feldspar porphyroclasts are intensively fractured and reduced to an ultrafine-grained mixture consisting of plagioclase and K-feldspar grains (< 15 µm) localized in C' shear bands. Detailed microstructural observations and electron backscatter diffraction (EBSD) analysis do not show evidence of intracrystalline plasticity in feldspar porphyroclasts and/or fluid-assisted replacement reactions. Quartz occurs either as thick (˜ 1-2 mm) monomineralic veins transposed along the shear zone foliation or as thin ribbons ( ≤ 25 µm width) dispersed in the feldspathic mixture. The microstructure and c axis crystallographic-preferred orientation are similar in the thick monomineralic veins and in the thin ribbons, and they suggest dominant subgrain rotation recrystallization and activity of prism < a > and rhomb < a > slip systems. However, the grain size in monophase recrystallized domains decreases when moving from the quartz monomineralic veins to the thin ribbons embedded in the feldspathic C' bands (14 µm vs. 5 µm respectively). The fine-grained feldspar mixture has a weak crystallographic-preferred orientation interpreted as the result of shear zone parallel-oriented growth during diffusion creep, as well as the same composition as the fractured porphyroclasts, suggesting that it generated by mechanical fragmentation of rigid porphyroclasts with a negligible role of chemical disequilibrium. Once C' shear bands were generated and underwent viscous deformation at constant stress conditions, the polyphase feldspathic aggregate would have deformed at a strain rate 1 order of magnitude faster than the monophase quartz monomineralic veins, as evidenced by applying experimentally and theoretically calibrated flow laws for dislocation creep in quartz and diffusion creep in

  19. Melting of metasomatized subcontinental mantle: New experiments and a new predictive models for plagioclase, spinel and garnet lherzolite melting

    NASA Astrophysics Data System (ADS)

    Grove, T. L.; Till, C. B.; Barr, J. A.; Krawczynski, M. J.

    2010-12-01

    Data from new experiments where liquid is in equilibrium with olivine + orthopyroxene + high-Ca clinopyroxene + Al-phase (plagioclase, spinel or garnet) have allowed us to recalibrate and update the melting model of Kinzler and Grove (K&G, JGR 97: 6885-6926, 1992) for melting under nominally anhydrous conditions over a larger range of pressure. We use existing literature data along with new experiments on melting of a high K2O primitive high alumina olivine tholeiite (HAOT) from the Oregon High Lava Plains, a high-K olivine leucitite from the Tibetan Plateau and low alkali, high FeO + MgO lunar ultramafic glasses. The new spinel lherzolite model is constrained by 114 experimental data that span a temperature range of 1200 to 1580 oC, a pressure range of 1 to 2.7 GPa and liquid alkali contents of up to 4.5 wt. % K2O and 5 wt. % Na2O. The garnet-lherzolite melting model uses 26 experimental constraints with new experiments containing up to 3.4 wt. % K2O. We use the following dependent variables to represent the melt composition in terms of oxygen-based mineral components: Olivine - Clinopyroxene - Plagioclase - Quartz and temperature. The independent variables are: pressure (P), molar Mg/(Mg+Fe) (Mg#), wt. % (K2O + Na2O)/(Na2O + K2O + CaO) (1-Ca#), wt.% Al2O3/(Al2O3+SiO2) (Al#), wt% K2O and wt. % TiO2. These variables describe the departure of melting behavior from the simplified lherzolite analog in CMAS (CaO-MgO-Al2O3-SiO2) in which melting behavior in univariant. This revised model facilitates a prediction of the liquid composition and temperature of multiple saturation with a mantle mineral assemblage for a given pressure. The new model allows compositional dependent calibration of the spinel to garnet lherzolite transition in sub-continental mantle environments. For example, beneath the Tibetan Plateau melting occurs near this transition and primitive high-K lavas show evidence of derivation from spinel- and garnet-bearing lherzolite. In addition, the HAOT lavas

  20. Origin of minor and trace element compositional diversity in anorthitic feldspar phenocrysts and melt inclusions from the Juan de Fuca Ridge

    USGS Publications Warehouse

    Adams, David T.; Nielsen, Roger L.; Kent, Adam J.R.; Tepley, Frank J.

    2011-01-01

    Melt inclusions trapped in phenocryst phases are important primarily due to their potential of preserving a significant proportion of the diversity of magma composition prior to modification of the parent magma array during transport through the crust. The goal of this investigation was to evaluate the impact of formational and post-entrapment processes on the composition of melt inclusions hosted in high anorthite plagioclase in MORB. Our observations from three plagioclase ultra-phyric lavas from the Endeavor Segment of the Juan de Fuca Ridge document a narrow range of major elements and a dramatically greater range of minor and trace elements within most host plagioclase crystals. Observed host/inclusion partition coefficients for Ti are consistent with experimental determinations. In addition, observed values of DTi are independent of inclusion size and inclusion TiO2 content of the melt inclusion. These observations preclude significant effects from the re-homogenization process, entrapment of incompatible element boundary layers or dissolution/precipitation. The observed wide range of TiO2 contents in the host feldspar, and between bands of melt inclusions within individual crystals rule out modification of TiO contents by diffusion, either pre-eruption or due to re-homogenization. However, we do observe comparatively small ranges for values of K2O and Sr compared to P2O5 and TiO2 in both inclusions and crystals that can be attributed to diffusive processes that occurred prior to eruption.

  1. Origin of plagioclase-olivine inclusions in carbonaceous chondrites

    NASA Astrophysics Data System (ADS)

    Sheng, Y. J.; Hutcheon, I. D.; Wasserburg, G. J.

    1991-02-01

    The origin of plagioclase-olivine inclusions (POIs) from three CV chondrites and one ungrouped chondrite was investigated by examining the chemical, mineralogical, and isotopic characteristics of a group of POIs from these chondrites. Results of these analyses demonstrate that the mixing and the partial melting processes in these inclusions were superimposed on more ancient isotopically heterogeneous material. A comparison of the essential characteristics of POIs and CAIs suggests that the major processes leading to the formation of POIs (such as condensation, dust/gas fractionation, aggregation of chemically and isotopically disparate materials, and partial melting) are common to most CAIs and chondrules. A scenario for the origin of POIs is proposed, showing that the homogeneity of the final assemblage (whether a POI, a CAI, or a chondrite) is primarily a reflection of the thermal history rather than the nature of precursor materials.

  2. Immersion Freezing of Potassium-feldspar and related Natural Samples

    NASA Astrophysics Data System (ADS)

    Zolles, Tobias; Burkart, Julia; Grothe, Hinrich

    2014-05-01

    Ice nucleation activities of mineral dust particles were investigated. The experiments were carried out using cryo-microscopy which is an oil-emulsion based method. The immersion freezing mode was addressed with this experimental setup. The studied samples were common inorganic atmospheric aerosols. Single minerals and natural samples were tested [1]. Mineral dust particles are active ice nuclei in the immersion freezing mode up to 256 K. Only recently potassium-feldspar has been identified as the by far most active ice nucleus followed by other silicates [2, 3]. Natural samples which contain more than 5% K-feldspar are also active. The activity of K-feldspar can be attributed to its surface structure and the presence of potassium ions in the surface. Ice nucleation on mineral dust particles takes place at certain nucleation sites. These sites are domains of molecular sites where water is stabilized in an ice-like structure. To form a good ice nucleation site, the site density of molecular sites needs to be high. More molecular sites are able to form larger domains on the surface, leading to better nucleation sites. This suggests further that the nucleation temperature of mineral dust particles scales with the surface area. The exact configuration of a molecular site is material specific and influenced by the local chemistry and structure of the dust particle surface. A favourable arrangement of the functional groups like surface hydroxyl and oxygen is proposed for the K-feldspar. Potassium ions seem to have a positive or neutral effect on the ice nucleation property of a silicate surface while cations with a higher charge density like calcium and sodium have a negative influence. K-feldspar is abundant in the environment and actually is the most important dust ice nucleus in the atmosphere. The nucleation temperatures of the K-feldspar particles are sufficient to enable further meteorological glaciation processes in high altitude clouds. References [1] Zolles, T

  3. Brittle grain size reduction of feldspar, phase mixing and strain localization in granitoids at mid-crustal conditions (Pernambuco shear zone, NE Brazil)

    NASA Astrophysics Data System (ADS)

    Viegas, Gustavo; Menegon, Luca; Archanjo, Carlos

    2016-04-01

    The Pernambuco shear zone (northeastern Brazil) is a large-scale strike-slip fault that, in its eastern segment, deforms granitoids at mid-crustal conditions. Initially coarse (> 50 μm) grained feldspar porphyroclasts are intensively fractured and reduced to an ultrafine-grained mixture consisting of plagioclase and K-feldspar grains (< 15 μm in size) localized in C' shear bands. Detailed microstructural observations and EBSD analysis do not show evidence of intracrystalline plasticity in feldspar porphyroclasts and/or fluid-assisted replacement reactions. Quartz occurs either as thick (˜ 1-2 mm) monomineralic bands or as thin ribbons dispersed in the feldspathic mixture. The microstructure and c-axis crystallographic preferred orientation are similar in the thick monomineralic band and in the thin ribbons, and suggest dominant subgrain rotation recrystallization and activity of prism and rhomb slip systems. However, the grain size in monophase recrystallized domains decreases when moving from the monomineralic veins to the thin ribbons embedded in the feldspathic C' bands (14 μm vs 5 μm, respectively).The fine-grained feldspar mixture has a weak crystallographic preferred orientation interpreted as the result of oriented growth during diffusion creep, as well as the same composition as the fractured porphyroclasts, suggesting that it generated by mechanical fragmentation of rigid porphyroclasts with a negligible role of chemical disequilibrium. Assuming that the C' shear bands deformed under constant stress conditions, the polyphase feldspathic aggregate would have deformed at a strain rate one order of magnitude faster than the monophase quartz ribbons. Overall, our dataset indicates that feldspar underwent a brittle-viscous transition while quartz was deforming via crystalline plasticity. The resulting rock microstructure consists of a two-phase rheological mixture (fine-grained feldspars and recrystallized quartz) in which the feldspathic material

  4. Diversity in the Visible-NIR Absorption Band Characteristics of Lunar and Asteroidal Plagioclase

    NASA Technical Reports Server (NTRS)

    Hiroi, T.; Kaiden, H.; Misawa, K.; Kojima, H.; Uemoto, K.; Ohtake, M.; Arai, T.; Sasaki, S.; Takeda, H.; Nyquist, L. E.; Shih, C.-Y.

    2012-01-01

    Studying the visible and near-infrared (VNIR) spectral properties of plagioclase has been challenging because of the difficulty in obtaining good plagioclase separates from pristine planetary materials such as meteorites and returned lunar samples. After an early study indicated that the 1.25 m band position of plagioclase spectrum might be correlated with the molar percentage of anorthite (An#) [1], there have been few studies which dealt with the band center behavior. In this study, the VNIR absorption band parameters of plagioclase samples have been derived using the modified Gaussian model (MGM) [2] following a pioneering study by [3].

  5. Thermoluminescence signal in K-feldspar grains: Revisited.

    PubMed

    Gong, Gelian; Sun, Weidong; Xu, Hongyun

    2015-11-01

    Recent work has shown that infrared stimulated luminescence (IRSL) signals in sedimentary coarse-grain K-feldspars are derived mainly from high temperature thermoluminescence (TL) peaks around 400°C, and the fading components of the IRSL signal can be preferentially removed by prior IR stimulation at relatively low temperature. Considering the complexity of TL signal for very old samples, we may choose non-fading components from K-feldspar TL signals using the combination of optical and thermal activation methods. This paper examines a protocol of post-IR isothermal TL (i.e. pIRITL) signal for sedimentary coarse-grain K-feldspars, which results from isothermal TL measurements following elevated temperature IR bleaching. We show that a sum of two exponential decay functions can fit well to the pIRITL decay curves, and both the holding temperature for isothermal TL measurements and the prior elevated temperature IR bleaching can affect greatly the fast components of pIRITL signal. The dose response ranges of pIRITL signal are wider than those of post-IR IRSL signals, but the relative high residual pIRITL signal means that it is not appropriate for dating young samples. It is expected that one isothermal TL signal for K-feldspar measured at ~400°C following IR bleaching at 290°C (i.e. pIRITL400) is useful for dating very old samples. PMID:26257084

  6. Thermoluminescence signal in K-feldspar grains: Revisited.

    PubMed

    Gong, Gelian; Sun, Weidong; Xu, Hongyun

    2015-11-01

    Recent work has shown that infrared stimulated luminescence (IRSL) signals in sedimentary coarse-grain K-feldspars are derived mainly from high temperature thermoluminescence (TL) peaks around 400°C, and the fading components of the IRSL signal can be preferentially removed by prior IR stimulation at relatively low temperature. Considering the complexity of TL signal for very old samples, we may choose non-fading components from K-feldspar TL signals using the combination of optical and thermal activation methods. This paper examines a protocol of post-IR isothermal TL (i.e. pIRITL) signal for sedimentary coarse-grain K-feldspars, which results from isothermal TL measurements following elevated temperature IR bleaching. We show that a sum of two exponential decay functions can fit well to the pIRITL decay curves, and both the holding temperature for isothermal TL measurements and the prior elevated temperature IR bleaching can affect greatly the fast components of pIRITL signal. The dose response ranges of pIRITL signal are wider than those of post-IR IRSL signals, but the relative high residual pIRITL signal means that it is not appropriate for dating young samples. It is expected that one isothermal TL signal for K-feldspar measured at ~400°C following IR bleaching at 290°C (i.e. pIRITL400) is useful for dating very old samples.

  7. (Energy related studies utilizing K-feldspar thermochronology)

    SciTech Connect

    Not Available

    1992-01-01

    In our second year of current funding cycle, we have investigated the Ar diffusion properties and microstructures of K-feldspars and the application of domain theory to natural K-feldspars. We completed a combined TEM and argon diffusion study of the effect of laboratory heat treatment on the microstructure and kinetic properties of K-feldspar. We conclude in companion papers that, with one minor exception, no observable change in the diffusion behavior occurs during laboratory extraction procedures until significant fusion occurs at about 1100{degrees}C. The effect that is observed involves a correlation between the homogenization of cryptoperthite lamelle and the apparent increase in retentivity of about 5% of the argon in the K-feldspar under study. We can explain this effect of both as an artifact of the experiment or the loss of a diffusion boundary. Experiments are being considered to resolve this question. Refinements have been made to our experimental protocol that appears that greatly enhance the retrieval of multi-activation energies from K-feldspars. We have applied the multi-domain model to a variety of natural environments (Valles Caldera, Red River fault, Appalachian basin) with some surprising results. Detailed {sup 40}Ar/{sup 39} Ar coverage of the Red River shear zone, thought to be responsible for the accommodation of a significant fraction of the Indo-Asian convergence, strongly suggests that our technique can precisely date both the termination of ductile strike-slip motion and the initiation of normal faulting. Work has continued on improving our numerical codes for calculating thermal histories and the development of computer based graphing tools has significantly increased our productivity.

  8. Alkali metal ionization detector

    DOEpatents

    Bauerle, James E.; Reed, William H.; Berkey, Edgar

    1978-01-01

    Variations in the conventional filament and collector electrodes of an alkali metal ionization detector, including the substitution of helical electrode configurations for either the conventional wire filament or flat plate collector; or, the substitution of a plurality of discrete filament electrodes providing an in situ capability for transferring from an operationally defective filament electrode to a previously unused filament electrode without removing the alkali metal ionization detector from the monitored environment. In particular, the helical collector arrangement which is coaxially disposed about the filament electrode, i.e. the thermal ionizer, provides an improved collection of positive ions developed by the filament electrode. The helical filament design, on the other hand, provides the advantage of an increased surface area for ionization of alkali metal-bearing species in a monitored gas environment as well as providing a relatively strong electric field for collecting the ions at the collector electrode about which the helical filament electrode is coaxially positioned. Alternatively, both the filament and collector electrodes can be helical. Furthermore, the operation of the conventional alkali metal ionization detector as a leak detector can be simplified as to cost and complexity, by operating the detector at a reduced collector potential while maintaining the sensitivity of the alkali metal ionization detector adequate for the relatively low concentration of alkali vapor and aerosol typically encountered in leak detection applications.

  9. Cordierite formation during the experimental reaction of plagioclase with Mg-rich aqueous solutions

    NASA Astrophysics Data System (ADS)

    Hövelmann, J.; Austrheim, H.; Putnis, A.

    2014-09-01

    The reaction between plagioclase (labradorite and oligoclase) and Mg-rich aqueous solutions was studied experimentally at hydrothermal conditions (600-700 °C, 2 kbar). During the experiments, plagioclase grains were readily converted to cordierite and quartz within 4 days. The cordierite crystals had well-developed polyhedral shapes, but showed skeletal internal morphologies suggesting that the initial growth occurred fast under high-driving-force conditions. In pure MgCl2 solutions (0.5-5 M), plagioclase dissolution and cordierite precipitation were spatially uncoupled indicating that Al was to some extent mobile in the fluid. Cordierite crystals formed at 700 °C showed orthorhombic symmetry, whereas those formed at 600 °C dominantly persisted in the metastable hexagonal form suggesting a strong increase in Al, Si ordering speed between 600 and 700 °C. The thermodynamic evolution of the fluid-solid system ultimately resulted in stabilization of Ca-rich plagioclase as demonstrated by partial anorthitization of unreacted plagioclase grains. Cordierite was also observed to form when Mg was added to a potentially albitizing Na-silicate-bearing solution. In that case, cordierite precipitation appeared to be more closely coupled to plagioclase dissolution, and secondary alteration of remnant plagioclase grains did not occur most likely due to armoring of the plagioclase by the cordierite overgrowth. The fast reaction rates observed in our experimental study have potential implications for Mg-metasomatism as a rock-forming process.

  10. Ion microprobe mass analysis of plagioclase from 'non-mare' lunar samples

    NASA Technical Reports Server (NTRS)

    Meyer, C., Jr.; Anderson, D. H.; Bradley, J. G.

    1974-01-01

    The ion microprobe was used to measure the composition and distribution of trace elements in lunar plagioclase, and these analyses are used as criteria in determining the possible origins of some nonmare lunar samples. The Apollo 16 samples with metaclastic texture and high-bulk trace-element contents contain plagioclase clasts with extremely low trace-element contents. These plagioclase inclusions represent unequilibrated relicts of anorthositic, noritic, or troctolitic rocks that have been intermixed as a rock flour into the KREEP-rich matrix of these samples. All of the plagioclase-rich inclusions which were analyzed in the KREEP-rich Apollo 14 breccias were found to be rich in trace elements. This does not seem to be consistent with the interpretation that the Apollo 14 samples represent a pre-Imbrium regolith, because such an ancient regolith should have contained many plagioclase clasts with low trace-element contents more typical of plagioclase from the pre-Imbrium crust. Ion-microprobe analyses for Ba and Sr in large plagioclase phenocrysts in 14310 and 68415 are consistent with the bulk compositions of these rocks and with the known distribution coefficients for these elements. The distribution coefficient for Li (basaltic liquid/plagioclase) was measured to be about 2.

  11. The origin of amorphous rims on lunar plagioclase grains: Solar wind damage or vapor condensates

    NASA Technical Reports Server (NTRS)

    Keller, Lindsay P.; Mckay, David S.

    1991-01-01

    A distinctive feature of micron sized plagioclase grains from mature lunar soils is a thin (20 to 100 nm) amorphous rim surrounding the grains. These rims were originally described from high voltage electron microscope observations of lunar plagioclase grains by Dran et al., who observed rims up to 100 nm thick on plagioclase grains from Apollo 11 and 12 soils. These rims are believed to be the product of solar wind damage. The amorphous rims were studied on micron sized plagioclase grains from a mature Apollo 16 soil using a JEOL 200FX transmission electron microscope equipped with an energy dispersive x ray spectrometer. It was found that the amorphous rims are compositionally distinct from the interior plagioclase and it is proposed that a major component of vapor condensates is present in the rims.

  12. Magmatic interactions as recorded in plagioclase phenocrysts of Chaos Crags, Lassen Volcanic Center, California

    USGS Publications Warehouse

    Tepley, F. J.; Davidson, J.P.; Clynne, M.A.

    1999-01-01

    The silicic lava domes of Chaos Crags in Lassen Volcanic National Park contain a suite of variably quenched, hybrid basaltic andesite magmatic inclusions. The inclusions represent thorough mixing between rhyodacite and basalt recharge liquids accompanied by some mechanical disaggregation of the inclusions resulting in crystals mixing into the rhyodacite host preserved by quenching on dome emplacement. 87Sr/86Sr ratios (~0.7037-0.7038) of the inclusions are distinctly lower than those of the host rhyodacite (~0.704-0.7041), which are used to fingerprint the origin of mineral components and to monitor the mixing and mingling process. Chemical, isotopic, and textural characteristics indicate that the inclusions are hybrid magmas formed from the mixing and undercooling of recharge basaltic magma with rhyodacitic magma. All the host magma phenocrysts (biotite, plagioclase, hornblende and quartz crystals) also occur in the inclusions, where they are rimmed by reaction products. Compositional and strontium isotopic data from cores of unresorbed plagioclase crystals in the host rhyodacite, partially resorbed plagioclase crystals enclosed within basaltic andesite inclusions, and partially resorbed plagioclase crystals in the rhyodacitic host are all similar. Rim 87Sr/86Sr ratios of the partially resorbed plagioclase crystals in both inclusions and host are lower and close to those of the whole-rock hybrid basaltic andesite values. This observation indicates that some crystals originally crystallized in the silicic host, were partially resorbed and subsequently overgrown in the hybrid basaltic andesite magma, and then some of these partially resorbed plagioclase crystals were recycled back into the host rhyodacite. Textural evidence, in the form of sieve zones and major dissolution boundaries of the resorbed plagioclase crystals, indicates immersion of crystals into a hotter, more calcic magma. The occurrence of partially resorbed plagioclase together with plagioclase

  13. Thermally-controlled luminescence signals from bedrock K-feldspars

    NASA Astrophysics Data System (ADS)

    Brown, N.; Rhodes, E. J.; Harrison, M.

    2015-12-01

    The proportion of electron-trapping sites within the crystal lattice of K-feldspar which are naturally filled by ionizing radiation is strongly dependent on temperature. Given that optically or thermally stimulated luminescence derives from these trapped electrons, luminescence signals from bedrock K-feldspar can be measured to determine whether a sample is in thermal steady state or disequilibrium. We therefore examine the natural degree of saturation for samples taken from: a) drill cores in regions which have been thermally static for most of the Cenozoic Era; b) a transect across a glacial valley which was excavated during the Last Glacial Maximum; and c) a rapidly-uplifting tectonic block along the San Andreas Fault. Finally, the utility of these signals for the purpose of low-temperature thermochronology is considered in terms of closure dynamics.

  14. Sr and Pb isotopic geochemistry of feldspars and implications for the growth of megacrysts in plutonic settings.

    NASA Astrophysics Data System (ADS)

    Munnikhuis, J.; Glazner, A. F.; Coleman, D. S.; Mills, R. D.

    2015-12-01

    Why megacrystic textures develop in silicic igneous rocks is still unknown. One hypothesis is that these crystals nucleate early in a magma chamber with a high liquid content. A supportive observation of this hypothesis is areas in plutons with high concentrations of megacrysts suggesting flow sorting. Another group of hypotheses suggest megacrystic textures form during protracted late-stage coarsening in a low-melt, interlocked matrix due to either thermal oscillations from incremental pluton emplacement, or Ostwald ripening. Isotopic analyses of large, euhedral K-feldspar megacrysts from the Cretaceous intrusive suites of the Sierra Nevada batholith (SNB) provide new insight into their origin. Megacrysts from the SNB reach the decimeter scale, are Or rich (85-90%), are perthitic, and host mineral inclusions of nearly all phases in the host rock. In-situ micro-drilling of transects, from core to rim, of the alkali feldspars provides material for Sr and Pb isotopic analyses by thermal ionization mass spectrometry (TIMS). Preliminary 87Sr/86Sr(i) isotopic data from samples from the Cathedral Peak Granodiorite, of the Tuolumne Intrusive Suite range from 0.706337 to 0.706452 (~1.6ɛSr) near the cores, whereas a sawtooth pattern with larger variability, 0.706179 to 0.706533 (~5ɛSr), occurs nears the rims. We interpret these preliminary data to indicate that the late portion of growth (i.e. crystal rim) was dominated by either cannibalism of small K-feldspar crystals with isotopic variability, or by addition of isotopically diverse late components to the magma. By comparing the Sr and Pb isotopic stratigraphy of megacrysts from a variety of rock matrices and different granitoids in the SNB isotopic trends can be evaluated to determine if crystals sizes are dependent on disequilibrium processes or grow at a steady state.

  15. OSL-thermochronometry of feldspar from the KTB borehole, Germany

    NASA Astrophysics Data System (ADS)

    Guralnik, Benny; Jain, Mayank; Herman, Frédéric; Ankjærgaard, Christina; Murray, Andrew S.; Valla, Pierre G.; Preusser, Frank; King, Georgina E.; Chen, Reuven; Lowick, Sally E.; Kook, Myungho; Rhodes, Edward J.

    2015-08-01

    The reconstruction of thermal histories of rocks (thermochronometry) is a fundamental tool both in Earth science and in geological exploration. However, few methods are currently capable of resolving the low-temperature thermal evolution of the upper ∼2 km of the Earth's crust. Here we introduce a new thermochronometer based on the infrared stimulated luminescence (IRSL) from feldspar, and validate the extrapolation of its response to artificial radiation and heat in the laboratory to natural environmental conditions. Specifically, we present a new detailed Na-feldspar IRSL thermochronology from a well-documented thermally-stable crustal environment at the German Continental Deep Drilling Program (KTB). There, the natural luminescence of Na-feldspar extracted from twelve borehole samples (0.1-2.3 km depth, corresponding to 10-70 °C) can be either (i) predicted within uncertainties from the current geothermal gradient, or (ii) inverted into a geothermal palaeogradient of 29 ± 2 °C km-1, integrating natural thermal conditions over the last ∼65 ka. The demonstrated ability to invert a depth-luminescence dataset into a meaningful geothermal palaeogradient opens new venues for reconstructing recent ambient temperatures of the shallow crust (<0.3 Ma, 40-70 °C range), or for studying equally recent and rapid transient cooling in active orogens (<0.3 Ma, >200 °C Ma-1 range). Although Na-feldspar IRSL is prone to field saturation in colder or slower environments, the method's primary relevance appears to be for borehole and tunnel studies, where it may offer remarkably recent (<0.3 Ma) information on the thermal structure and history of hydrothermal fields, nuclear waste repositories and hydrocarbon reservoirs.

  16. Investigating the origin of anorthitic plagioclase through a combination of experiments and natural observations

    NASA Astrophysics Data System (ADS)

    Lundstrom, Craig C.; Tepley, Frank J.

    2006-09-01

    The origin of anorthitic plagioclase in volcanic rocks worldwide remains an enigma. Arenal volcano, Costa Rica, provides a good example of the problem: up to An 96 plagioclase are found within moderately evolved basaltic andesites. We follow up a recent suggestion [Lundstrom, C.C., Boudreau, A., Pertermann, M., 2005. Diffusion-reaction in a thermal gradient: Implications for the genesis of anorthitic plagioclase, high alumina basalt and igneous mineral layering. Earth Planet. Sci. Lett. 237, 829-854] that diffusion-reaction processes occurring between ascending magmas and gabbroic wall rocks might provide a means of producing anorthitic plagioclase without requiring exotic, ultra-calcic melt compositions by integrating observations from three analytical methods: (1) laboratory diffusion-reaction experiments in the diopside-albite-anorthite (DAA) system; (2) transmission electron microscopy (TEM) of plagioclase grains from both a diffusion-reaction experiment and an Arenal lava; and (3) Sr isotope microstratigraphy of phenocrysts and megacrysts from natural lavas from the current eruption at Arenal. Two plagioclase saturated DAA melts, juxtaposed in experiments at either 1 bar pressure (anhydrous) or at 0.5 GPa pressure (hydrous) for 3-5 days at 1244 or 1125 °C, illustrate the dramatic effect of H 2O on facilitating plagioclase reaction. In the presence of wet melt, enrichment in anorthitic plagioclase occurs at the material interface while in the presence of the dry 1 bar melt, plagioclase shows no reaction. TEM analyses of a homogeneous anorthitic plagioclase from a diffusion-reaction experiment indicates heterogeneous columns of more anorthite-rich plagioclase at the < 100 nm scale while a homogeneous anorthitic plagioclase phenocryst from a 1968 lava from Arenal found much of the crystal to be composed of 20-50 μm diameter subgrains, having ˜ 1 μm diameter tubes filled with Fe, K, Si-rich glass. Large core-rim variations in 87Sr/ 86Sr occur within three

  17. Crystallization of An-rich plagioclase in 'dacitic' melt at Arenal volcano: Natural occurrence and experiments

    NASA Astrophysics Data System (ADS)

    Parat, F.; Streck, M.; Holtz, F.; Almeev, R.

    2006-12-01

    High-An plagioclase (An85-94) is ubiquitous in crystal-rich basaltic andesitic lavas of the current eruption and of the entire eruptive history of Arenal volcano, Costa Rica. An85-91 plagioclase was found to host glassy melt inclusions of dacitic composition suggesting that high An plagioclase may also crystallize in melts as silicic as ~63 wt.% SiO2 (Streck &Wacaster, 2006). Such dacitic melt inclusion compositions resemble dacite tephra units that erupted a few times in Arenal's history. We investigated one pumice clast from the dacitic ET2 tephra (e.g. Borgia et al., 1988) to shed light on the possibility to crystallize high An plagioclase from dacitic melt. The natural ET2 pumice sample is phenocryst poor (~7 wt.%) with a fine-grained, vesicular, and mostly crystalline matrix. Phenocrysts are dominated by plagioclase with subordinate amphibole, pyroxenes and oxides. Apatite occurs as accessory phase. Plagioclase cores indeed display high An between An94 to An85. On the other hand, rim compositions tend to be significantly less anorthitic (~An75 to 65). A natural glass made from a split of the natural ET2 pumice clast was utilized as starting material for an experimental investigation into phase equilibria of this dacite magma. The first experiments were carried out at high pressure (4 kbar), high temperature (900-950°C) and water-rich conditions (4-9 wt.% H2O in melt) in an internally heated pressure vessel (ΔlogfO2~NNO+3). Plagioclase with up to 83 mole % anorthite crystallizes at 900°C and for H2Omelt=9 wt.% (water-saturated). An-rich plagioclase coexists with amphibole (Mg#~70) and magnetite (Xulvo=10) in 60 wt.% SiO2 melt. As expected, An content increases with increasing temperature and water content in the melt. At 950°C, current experiments found plagioclase (An75) to be stable with H2Omelt<6.4 wt.% (no plagioclase at water-saturated conditions, only magnetite crystallizes). We infer that plagioclase begins crystallizing at H2Omelt = 8 wt.% and is

  18. Particle size and X-ray analysis of Feldspar, Calvert, Ball, and Jordan soils

    NASA Technical Reports Server (NTRS)

    Chapman, R. S.

    1977-01-01

    Pipette analysis and X-ray diffraction techniques were employed to characterize the particle size distribution and clay mineral content of the feldspar, calvert, ball, and jordan soils. In general, the ball, calvert, and jordan soils were primarily clay size particles composed of kaolinite and illite whereas the feldspar soil was primarily silt-size particles composed of quartz and feldspar minerals.

  19. Effects of changing H2O concentrations and viscosities on plagioclase crystallization in a rhyolite obsidian: experiments and plagioclase speedometry (Invited)

    NASA Astrophysics Data System (ADS)

    Waters, L.; Andrews, B. J.; Lange, R. A.

    2013-12-01

    H2O-saturated phase equilibrium and decompression experiments on a rhyolite obsidian (73 wt% SiO2) from Medicine Lake Volcano, CA demonstrate the effect of changing melt H2O concentrations and melt viscosity on plagioclase crystallization. The natural sample is saturated in plagioclase + orthopyroxene + ilmenite + magnetite + apatite + zircon, despite low phenocryst abundances (<2.3%) and no microlite crystallization. Eruptive temperature and oxygen fugacity (×1σ), on the basis of Fe-Ti oxide thermometry, are 852 × 12°C and ΔNNO +0.3 × 0.1. Plagioclase compositions range from 33-53 mol% An. Given the low crystallinity and absence of significant cooling, the progressive loss of dissolved melt H2O during ascent best explains the broad range in phenocryst composition and the low crystallinity. Phase equilibrium experiments were conducted at temperatures and pressures ranging from 750-950°C and 50-300 MPa, respectively. Experiments were conducted in a Ni-rich pressure vessel (Waspaloy) with Ni filler rod, which produces an intrinsic fO2 of ΔNNO +1 × 0.5 (Geshwind & Rutherford, 1992) and pressurized with H2O (where Ptotal= PH2O). The results of the phase equilibrium experiments show that the most anorthitic plagioclase crystallized at ~3.95 wt% H2O and the most albitic at ~3.49 wt% H2O. Plagioclase crystallization in the natural sample ceased at relatively high melt H2O content (3.49 wt%), which corresponds to a viscosity of 4.85 log10 Pa s (Hui & Zhang, 2007). To evaluate the effect of decompression rate on plagioclase crystallization, experiments were conducted on the rhyolite at two different continuous decompression rates, 3.0 MPa/hr and 0.8 MPa/hr. Two decompression experiments were conducted for each rate over two pressure interals:150 to 89 MPa and from 150 to 58 MPa. The results from our study are combined with the results of single- and multi-step decompression experiments on rhyolites/rhyodacites from Geshwind & Rutherford (1995), Couch et al., (2003

  20. Apparatus enables accurate determination of alkali oxides in alkali metals

    NASA Technical Reports Server (NTRS)

    Dupraw, W. A.; Gahn, R. F.; Graab, J. W.; Maple, W. E.; Rosenblum, L.

    1966-01-01

    Evacuated apparatus determines the alkali oxide content of an alkali metal by separating the metal from the oxide by amalgamation with mercury. The apparatus prevents oxygen and moisture from inadvertently entering the system during the sampling and analytical procedure.

  1. Naturally weathered feldspar surfaces in the Navajo Sandstone aquifer, Black Mesa, Arizona: Electron microscopic characterization

    USGS Publications Warehouse

    Zhu, Chen; Veblen, D.R.; Blum, A.E.; Chipera, S.J.

    2006-01-01

    Naturally weathered feldspar surfaces in the Jurassic Navajo Sandstone at Black Mesa, Arizona, was characterized with high-resolution transmission and analytical electron microscope (HRTEM-AEM) and field emission gun scanning electron microscope (FEG-SEM). Here, we report the first HRTEM observation of a 10-nm thick amorphous layer on naturally weathered K-feldspar in currently slightly alkaline groundwater. The amorphous layer is probably deficient in K and enriched in Si. In addition to the amorphous layer, the feldspar surfaces are also partially coated with tightly adhered kaolin platelets. Outside of the kaolin coatings, feldspar grains are covered with a continuous 3-5 ??m thick layer of authigenic smectite, which also coats quartz and other sediment grains. Authigenic K-feldspar overgrowth and etch pits were also found on feldspar grains. These characteristics of the aged feldspar surfaces accentuate the differences in reactivity between the freshly ground feldspar powders used in laboratory experiments and feldspar grains in natural systems, and may partially contribute to the commonly observed apparent laboratory-field dissolution rate discrepancy. At Black Mesa, feldspars in the Navajo Sandstone are dissolving at ???105 times slower than laboratory rate at comparable temperature and pH under far from equilibrium condition. The tightly adhered kaolin platelets reduce the feldspar reactive surface area, and the authigenic K-feldspar overgrowth reduces the feldspar reactivity. However, the continuous smectite coating layer does not appear to constitute a diffusion barrier. The exact role of the amorphous layer on feldspar dissolution kinetics depends on the origin of the layer (leached layer versus re-precipitated silica), which is uncertain at present. However, the nanometer thin layer can be detected only with HRTEM, and thus our study raises the possibility of its wide occurrence in geological systems. Rate laws and proposed mechanisms should consider the

  2. Magma mixing, recharge and eruption histories recorded in plagioclase phenocrysts from El Chichon Volcano, Mexico

    USGS Publications Warehouse

    Tepley, F. J.; Davidson, J.P.; Tilling, R.I.; Arth, Joseph G.

    2000-01-01

    Consistent core-to-rim decreases of 87Sr/86Sr ratios and coincident increases in Sr concentrations in plagioclase phenocrysts of varying size (~ 1 cm to 2 mm) are reported from samples of the 1982 and pre-1982 (~ 200 ka) eruptions of El Chichon Volcano. Maximum 87Sr/86Sr ratios of ~ 0.7054, significantly higher than the whole-rock isotopic ratios (~ 0.7040-0.7045), are found in the cores of plagioclase phenocrysts, and minimum 87Sr/86Sr ratios of ~ 0.7039 are found near some of the rims. Plagioclase phenocrysts commonly display abrupt fluctuations in An content (up to 25 mol %) that correspond to well-developed dissolution surfaces The isotopic, textural and compositional characteristics suggest that these plagioclase phenocrysts grew in a system that was periodically recharged by higher-temperature magma with a lower 87Sr/86Sr ratio and a higher Sr concentration. Rim 87Sr/86Sr ratios in plagioclase phenocrysts of rocks from the 200 ka eruption indicate that, at that time, the magma had already attained the lowest recorded 87Sr/86Sr value of the system (~ 0.7039). In contrast, cores from plagioclase phenocrysts of the 1982 eruption, inferred to have grown in the past few thousand years, have the highest recorded 87Sr/86Sr ratios of the system. Collectively, the Sr isotopic data (for plagioclase and whole rock), disequilibrium textural features of the phenocrysts, known eruption frequencies, and inferred crystal-residence times of the plagioclases are best interpreted in terms of an intermittent magma chamber model. Similar processes, including crustal contamination, magma mixing, periodic recharge by addition of more mafic magma to induce plagioclase disequilibrium (possibly triggering eruption) and subsequent re-equilibration, apparently were operative throughout the 200 ky history of the El Chichon magma system.

  3. Aureoles of Pb(II)-enriched feldspar around monazite in paragneiss and anatectic pods of the Napier Complex, Enderby Land, East Antarctica: the roles of dissolution-reprecipitation and diffusion

    NASA Astrophysics Data System (ADS)

    Grew, Edward S.; Yates, Martin G.; Wilson, Christopher J. L.

    2008-03-01

    Extraordinarily high Pb content in K-feldspar and plagioclase has been found contiguous to monazite in two occurrences in the ultrahigh-temperature Napier Complex of Antarctica. Monazite shows a variety of textures and compositions. In a garnet-sillimanite-orthopyroxene paragneiss at Mount Pardoe (Amundsen Bay), grains range 80 150 μm across and are anhedral; two grains are Th- and Si-dominant. In pods that crystallized from anatectic melts at 2500 Ma at Zircon Point, Casey Bay, monazite grains range 0.05 mm 1 cm in length and are highly variable in texture. The coarsest grains (>0.7 cm) are skeletal and euhedral, whereas the smallest grains are anhedral and associated with fine- to medium-grained quartz, K-feldspar, plagioclase, garnet, sillimanite and rutile in aggregates that form interstitial veinlets interpreted to be a second generation of anatexis during an event at 1100 Ma. The huttonite component (ThSiO4) reaches 30 mole% in the cores of the coarsest skeletal grains, whereas other grains, particularly smaller ones, show complex and irregular zoning in Th and U. The latter zoning is attributed to dissolution-reprecipitation, which also resulted in complete Pb loss during the 1100 Ma event. In the paragneiss at Mount Pardoe, K-feldspar and myrmekitic plagioclase (An16) are found in a 70 80 μm band between monazite and orthopyroxene and contain up to 12.7 wt.% and 2.7 wt.% PbO, respectively, corresponding to 18.5% and 3.4% PbAl2Si2O8 component, respectively. Cathodoluminescence of both feldspars increases with distance from a nearby monazite grain and is not correlated with Pb content. Incorporation of Pb in K-feldspar and plagioclase could be a result of diffusion, even though the monazite adjacent to feldspar apparently lost little Pb, i.e., Pb could have been transported by fluid from the Th-rich grains, which did lose Pb. In contrast to the paragneiss, cathodoluminescence correlates with Pb content of K-feldspar in aureoles surrounding skeletal monazite

  4. Alkali metal ion battery with bimetallic electrode

    SciTech Connect

    Boysen, Dane A; Bradwell, David J; Jiang, Kai; Kim, Hojong; Ortiz, Luis A; Sadoway, Donald R; Tomaszowska, Alina A; Wei, Weifeng; Wang, Kangli

    2015-04-07

    Electrochemical cells having molten electrodes having an alkali metal provide receipt and delivery of power by transporting atoms of the alkali metal between electrode environments of disparate chemical potentials through an electrochemical pathway comprising a salt of the alkali metal. The chemical potential of the alkali metal is decreased when combined with one or more non-alkali metals, thus producing a voltage between an electrode comprising the molten the alkali metal and the electrode comprising the combined alkali/non-alkali metals.

  5. Methods of recovering alkali metals

    DOEpatents

    Krumhansl, James L; Rigali, Mark J

    2014-03-04

    Approaches for alkali metal extraction, sequestration and recovery are described. For example, a method of recovering alkali metals includes providing a CST or CST-like (e.g., small pore zeolite) material. The alkali metal species is scavenged from the liquid mixture by the CST or CST-like material. The alkali metal species is extracted from the CST or CST-like material.

  6. Chlor-Alkali Technology.

    ERIC Educational Resources Information Center

    Venkatesh, S.; Tilak, B. V.

    1983-01-01

    Chlor-alkali technology is one of the largest electrochemical industries in the world, the main products being chlorine and caustic soda (sodium hydroxide) generated simultaneously by the electrolysis of sodium chloride. This technology is reviewed in terms of electrochemical principles and manufacturing processes involved. (Author/JN)

  7. The Petrographic Distinction between Basalt and Andesite Based upon the Arrested Fractionation of Plagioclase Phenocrysts.

    ERIC Educational Resources Information Center

    Garlick, G. Donald; Garlick, Benjamin J.

    1987-01-01

    Discusses the need to take into account the effects of arrested fractional crystallization in the petrographic classification of volcanic rocks containing plagioclase phenocrysts. Describes the development and use of a computer program to accomplish this task graphically. (TW)

  8. Selective Dissolution of Plagioclase in Semarkona: Low-Temperature Fluid-Solid Interactions

    NASA Astrophysics Data System (ADS)

    Dobrica, E.; Brearley, A. J.

    2016-08-01

    We are focusing on evidence of aqueous alteration at the boundary between matrix lumps and chondrule phenocrysts. This study shows that dissolution of plagioclase can take place at the lower metamorphic temperatures experienced by Semarkona.

  9. Mg in plagioclase: Experimental calibration of a new geothermometer and diffusion coefficients

    NASA Astrophysics Data System (ADS)

    Faak, Kathrin; Chakraborty, Sumit; Coogan, Laurence A.

    2013-12-01

    The temperature-sensitive exchange of Mg between plagioclase (Pl) and clinopyroxene (Cpx) has been studied experimentally, accounting for different anorthite-contents in plagioclase (XAn) and various silica activities (aSiO2) in the system. The partitioning of Mg between plagioclase and clinopyroxene was determined over a temperature range of 1100-1200 °C, using plagioclase single crystals of different compositions (XAn = 0.5-0.8), surrounded by different clinopyroxene-bearing matrix powders to account for different silica activities from 0.55 to 1.0. The experimental design also allows the diffusivity (DMgPl) of Mg in plagioclase under these conditions to be determined. Both KMgPl/Cpx (defined as KMgPl/Cpx=CMgPl/CMgCpx) and DMgPl decrease with temperature and increase with aSiO2. Isothermal data for different XAn in plagioclase show a linear increase of ln KMgPl/Cpx with increasing XAn, but DMgPl appears to be insensitive to XAn. The partitioning data allow a new geothermometer to be calibrated, which may be widely applicable to terrestrial and extraterrestrial rocks where plagioclase and clinopyroxene coexist: T[K]=(-9219+2034XAn)/(ln KMgPl/Cpx-1.6-ln aSiO2). Application of this geothermometer to experimental data from this study reproduces the experimental temperatures within ±20 °C. Diffusion of Mg in plagioclase is described by DMgPl[m s]=1.25×10-4[ms]·exp(-320,924[J mol]/(RT))·(.

  10. Oxygen isotopic determinations of sequentially erupted plagioclases in the 1974 magma of Fuego Volcano, Guatemala

    USGS Publications Warehouse

    Rose, W.I.; Friedman, I.; Woodruff, L.G.

    1980-01-01

    Plagioclases in the 1974 high-Al basalt from Fuego Volcano have ??O18 values of +6.0 to +8.5 per mil. Meteoric water cannot have played a significant role in Fuego's magma. Large, weakly zone clear phenocrysts had ??O18 values in the accepted mantle range, while patchyzoned and oscillatory-zoned plagioclases inferred to have formed later and shallower levels have slightly heavier oxygen isotopic ratios. ?? 1980 Intern. Association of Volcanology and Chemistry of the Earth's Interior.

  11. Deconvolution of mixtures with high plagioclase content for the remote interpretation of lunar plagioclase-rich regions

    NASA Astrophysics Data System (ADS)

    Serventi, Giovanna; Carli, Cristian; Sgavetti, Maria

    2016-07-01

    Anorthositic rocks are widespread on the lunar surface and have probably been formed by flotation of PL over a magma ocean. A large portion of pristine rocks are characterized by a low Mg/(Mg+Fe) ratio, and have been classified as ferroan anorthosite, and recently, after observation from SELENE Spectral Profiler,pure anorthosites regions with more than 98% PL have been recognized. In this paper, we analyze a set of mixtures with PL content similar to the ferroan anorthosites and to the pure anorthosite regions, using the Origin Software and the Modified Gaussian Model. We consider three plagioclases with varying FeOwt% contents (PL1, PL2 and PL3)andthree mafic end-members (1) 100% orthopyroxene, (2) 56% orthopyroxene and 44% clinopyroxene, and (3) 100% olivine (OL). The spectral parameters considered here are: band depth, band center, band width, c0 (the continuum intercept) and c1 (the continuum offset). Here we have shown that in pyroxene (PX)-bearing mixtures, the PX is distinguishable even in mixtures with only 1% PX and that PX band at ca. 900 nm is always deeper than PL1 band while PL2 and PL3 are deeperthan OPX 900 nm band from 95, 96% PL. In OL-bearing mixtures, OL detection limit is 2% when mixed with PL1, and 3% and 4% if mixed with PL2 and PL3. We also demonstrated how spectral parameters vary with PL%, and, generally, increasing the PL content: (1) 1250 nm band depth decreases when mixed with OL, while it deepens in mixtures with PX; (2) 1250 nm band centers generally move towards longer wavelength for PL1-bearing mixtures, while do not show significant variations considering PL2/PL3-mixtures; (3) 1250 nm band width of PL1 in E1 and E5-mixtures substantially widens while in other mixtures it only slightly varies. Here we also proposed an application to a real case, from Proclus crater, revealing how studying terrestrial analogues is fundamental to infer hypothesis on the mineralogical composition of a planetary surface, but also how the spectral

  12. Early differentiation of the moon - Evidence from trace elements in plagioclase

    SciTech Connect

    Palme, H.; Spettel, B.

    1984-11-15

    Bulk samples and plagioclase mineral grains from lunar cataclastic ferroan anorthosites were analyzed for trace elements by instrumental neutron activation analysis. Some pure plagioclase crystals have lower concentrations of Cr, Co, Sc, and heavy REEs than previous analyses indicated. Concentrations of Sr, Eu, Na, Ga, and the REEs in plagioclases from different anorthosites vary in a systematic way, and the trace element patterns of plagioclases from pristine norites and troctolites are very different from the plagioclase pattern of anorthosites. The following model is suggested to account for these observations: (1) melting of a large fraction of the moon, formation of a magma ocean, precipitation of olivine and later pyroxene, followed by flotation of cumulus plagioclase; (2) mixing of KREEP with a mafic component enriched in Mg, Cr, and Co; (3) precipitation of noritic and troctolitic cumulates and metallic iron from this magma; and (4) eruption of these KREEP and Mg-rich lavas and/or distribution of these materials over the front-side of the moon by basin-forming impacts 3.9-4.0 b.y. ago.

  13. Microstructural investigation of the interaction and interdependence of cataclastic and plastic mechanisms in Feldspar crystals deformed in the semi-brittle field

    NASA Astrophysics Data System (ADS)

    McLaren, A. C.; Pryer, L. L.

    2001-06-01

    Plagioclase feldspar (An 50) single crystals from the Hogarth Range, NSW, Australia, have been deformed in the brittle-to-semi-brittle regime at 500-800 °C, 90-300 MPa effective pressure, and strain rate between 10 -5 and 10 -6. This gem quality feldspar is both macroscopically and microscopically devoid of any microstructure other than very rare growth twins, so all microstructures produced by experimental deformation can be easily identified. The specimens were deformed to failure, which occurred at strains of <4%, and exhibit microstructures of interacting albite twins and microcracks. The shear stress at the tip of a propagating shear fracture is relieved through the production of mechanical twins. Similarly, the elastic strain in a twin is replaced by a microcrack. In addition to the very important role of relieving stress at the tips of shear fractures, groups of twins also accommodate lattice misorientations of several degrees, typical of those seen in subgrains that have been produced by dislocation climb. These observations suggest that the deformation progressed by an alternation of twinning and microfracturing, each process initiating the other in turn. Tangled and isolated dislocations were also observed in and near partially healed cracks. Since, in other materials, dislocation tangles have been observed to nucleate cracks, our observations suggest that in general, deformation to higher strains in the semi-brittle regime is probably controlled, not by the simple superposition of brittle and plastic processes operating independently, but by their interaction and interdependence.

  14. Hydrothermal alkali metal recovery process

    DOEpatents

    Wolfs, Denise Y.; Clavenna, Le Roy R.; Eakman, James M.; Kalina, Theodore

    1980-01-01

    In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles by treating them with a calcium or magnesium-containing compound in the presence of water at a temperature between about 250.degree. F. and about 700.degree. F. and in the presence of an added base to establish a pH during the treatment step that is higher than would otherwise be possible without the addition of the base. During the treating process the relatively high pH facilitates the conversion of water-insoluble alkali metal compounds in the alkali metal residues into water-soluble alkali metal constituents. The resultant aqueous solution containing water-soluble alkali metal constituents is then separated from the residue solids, which consist of the treated particles and any insoluble materials formed during the treatment step, and recycled to the gasification process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. Preferably, the base that is added during the treatment step is an alkali metal hydroxide obtained by water washing the residue solids produced during the treatment step.

  15. Low-temperature multi-OSL-thermochronometry of feldspar

    NASA Astrophysics Data System (ADS)

    King, Georgina; Herman, Frederic; Lambert, Renske; Valla, Pierre; Guralnik, Benny

    2016-04-01

    Constraining exhumation rates and landscape histories over Quaternary timescales represents a major challenge for understanding the interaction between changing climate and erosion processes. Facilitated by closure temperatures of as low as ~30 C, OSL-thermochronometry is able to constrain cooling rates from the top few km of the earth's crust, and offers the potential for recent changes in erosion to be determined. Based on the well-established Quaternary dating technique of optically stimulated luminescence dating, OSL-thermochronometry benefits from a strong methodological and theoretical foundation. A further advantage of OSL-thermochronometry is that it is possible to measure multiple luminescence signals from a single mineral, such as feldspar. Therefore OSL-thermochronometry can be used as a multi-thermochronometer whereby different signals from the same mineral have closure temperatures in the range of 30-70 C, enabling the derivation of very precise cooling histories. However, in contrast to other low-temperature methods, OSL-thermochronometry is limited by signal saturation, restricting its application to either elevated temperature settings (e.g. bore holes, tunnels) or rapidly exhuming terranes. Here we outline the principles of multi-OSL-thermochronometry of feldspar and its potential as a low-temperature thermochronometry system.

  16. Alkali-vapor lasers

    NASA Astrophysics Data System (ADS)

    Zweiback, J.; Komashko, A.; Krupke, W. F.

    2010-02-01

    We report on the results from several of our alkali laser systems. We show highly efficient performance from an alexandrite-pumped rubidium laser. Using a laser diode stack as a pump source, we demonstrate up to 145 W of average power from a CW system. We present a design for a transversely pumped demonstration system that will show all of the required laser physics for a high power system.

  17. Ultramafic inclusions and host alkali olivine basalts of the southern coastal plain of the Red Sea, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Ghent, Edward D.; Coleman, Robert Griffin; Hadley, Donald G.

    1979-01-01

    A variety of mafic and ultramafic inclusions occur within the pyroclastic components of the Al Birk basalt, erupted on the southern Red Sea coastal plain of Saudi Arabia from Pleistocene time to the present. Depleted harzburgites are the only inclusions contained within the basalts that were erupted through Miocene oceanic crust (15 km thick) in the vicinity of Jizan, whereas to the north in the vicinity of Al Birk, alkali basalts that were erupted through a thicker Precambrian crust (48 km thick) contain mixtures of harzburgites, cumulate gabbro, and websterite inclusions accompanied by large (> 2 cm) megacrysts of glassy alumina-rich clinopyroxene, plagioclase, and spinel. Microprobe analyses of individual minerals from the harzburgites, websterites, and cumulate gabbros reveal variations in composition that can be related to a complex mantle history during the evolution of the alkali basalts. Clinopyroxene and plagioclase megacrysts may represent early phases that crystallized from the alkali olivine basalt magma at depths less than 35 km. Layered websterites and gabbros with cumulate plagioclase and clinopyroxene may represent continuing crystallization of the alkali olivine basalt magma in the lower crust when basaltic magma was not rapidly ascending. It is significant that the megacrysts and cumulate inclusions apparently form only where the magmas have traversed the Precambrian crust, whereas the harzburgite-bearing basalts that penetrated a much thinner Miocene oceanic crust reveal no evidence of mantle fractionation. These alkali olivine basalts and their contained inclusions are related in time to present-day rifting in the Red Sea axial trough. The onshore, deep-seated, undersaturated magmas are separated from the shallow Red Sea rift subalkaline basalts by only 170 km. The contemporaneity of alkaline olivine and subalkaline basalts requires that they must relate directly to the separation of the Arabian plate from the African plate.

  18. Controls on polyacrylamide adsorption to quartz, kaolinite, and feldspar

    SciTech Connect

    Graveling, G.J.; Ragnarsdottir, K.V.; Allen, G.C.

    1997-09-01

    Potentiometric titrations of quartz, kaolinite, feldspar, and partially hydrolysed polyacrylamide (HPAM), and sorption measurements of HPAM on the minerals, allows identification of the general mechanisms of polyacrylamide adsorption to aluminosilicates and quartz. Adsorption was monitored at the mineral solution interface by way of X-ray photoelectron spectroscopy (XPS). XPS spectra of the unreacted minerals show bands in the Ols, Si2p, Al2p, and Cls regions. Additional peaks are observed in the Cls and N1s regions after treatment with polyacrylamide and the latter is used in this study to monitor corresponding to surface site saturation. At a fixed polymer concentration, adsorption varies with pH-dependent surface charge. The adsorption mechanism changes with pH, reflecting variation in the pH-dependent concentrations of ionizable groups on polyacrylamide and at aluminosilicate surfaces, and the extent of hydrogen-bonding between uncharged mineral surface sites and polymer amide groups. 42 refs., 10 figs., 2 tabs.

  19. Is plagioclase removal responsible for the negative Eu anomaly in the source regions of mare basalts

    SciTech Connect

    Shearer, C.K.; Papike, J.J. )

    1989-12-01

    The nearly ubiquitous presence of a negative Eu anomaly in the mare basalts has been suggested to indicate prior separation and flotation of plagioclase from the basalt source region during its crystallization from a lunar magma ocean (LMO). Are there any mare basalts derived from a mantle source which did not experience prior plagioclase separation Crystal chemical rationale for REE substitution in pyroxene suggests that the combination of REE size and charge, M2 site characteristics of pyroxene, fO{sub 2}, magma chemistry, and temperature may account for the negative Eu anomaly in the source region of some types of primitive, low TiO{sub 2} mare basalts. This origin for the negative Eu anomaly does not preclude the possibility of the LMO as many mare basalts still require prior plagioclase crystallization and separation and/or hybridization involving a KREEP component.

  20. Is plagioclase removal responsible for the negative Eu anomaly in the source regions of mare basalts?

    NASA Technical Reports Server (NTRS)

    Shearer, C. K.; Papike, J. J.

    1989-01-01

    The nearly ubiquitous presence of a negative Eu anomaly in the mare basalts has been suggested to indicate prior separation and flotation of plagioclase from the basalt source region during its crystallization from a lunar magma ocean (LMO). Are there any mare basalts derived from a mantle source which did not experience prior plagioclase separation? Crystal chemical rationale for REE substitution in pyroxene suggests that the combination of REE size and charge, M2 site characteristics of pyroxene, fO2, magma chemistry, and temperature may account for the negative Eu anomaly in the source region of some types of primitive, low TiO2 mare basalts. This origin for the negative Eu anomaly does not preclude the possibility of the LMO as many mare basalts still require prior plagioclase crystallization and separation and/or hybridization involving a KREEP component.

  1. SCR and GCR exposure ages of plagioclase grains from lunar soil

    NASA Technical Reports Server (NTRS)

    Etique, P.; Baur, H.; Signer, P.; Wieler, R.

    1986-01-01

    The concentrations of solar wind implanted Ar-36 in mineral grains extracted from lunar soils show that they were exposed to the solar wind on the lunar surface for an integrated time of 10E4 to 10E5 years. From the bulk soil 61501 plagioclase separates of 8 grain size ranges was prepared. The depletion of the implanted gases was achieved by etching aliquot samples of 4 grain sizes to various degrees. The experimental results pertinent to the present discussion are: The spallogenic Ne is, as in most plagioclases from lunar soils, affected by diffusive losses and of no use. The Ar-36 of solar wind origin amounts to (2030 + or - 100) x 10E-8 ccSTP/g in the 150 to 200 mm size fraction and shows that these grains were exposed to the solar wind for at least 10,000 years. The Ne-21/Ne-22 ratio of the spallogenic Ne is 0.75 + or - 0.01 and in very good agreement with the value of this ratio in a plagioclase separate from rock 76535. This rock has had a simple exposure history and its plagioclases have a chemical composition quite similar to those studied. In addition to the noble gases, the heavy particle tracks in an aliquot of the 150 to 200 mm plagioclase separate were investigated and found 92% of the grains to contain more than 10E8 tracks/sq cm. This corresponds to a mean track density of (5 + or - 1) x 10E8 tracks/sq cm. The exploration of the exposure history of the plagioclase separates from the soil 61501 do not contradict the model for the regolith dynamics but also fail to prove it.

  2. Uptaking of plagioclase xenocryst into H2O-rich rear-arc basaltic magma

    NASA Astrophysics Data System (ADS)

    Hamada, M.

    2015-12-01

    Kuritani et al. (2013, Mineral. Petrol.) and Kuritani et al. (2014, Contrib. Mineral. Petrol.) estimated genetic conditions of primary arc magmas beneath the Iwate volcano (a frontal arc volcano in the northeast Japan arc) and the Sannome-gata volcano (a rear-arc volcano in the northeast Japan arc) based on analyses of volcanic rocks and numerical simulation. They estimated that H2O concentrations of primary melts are 4-5 wt.% beneath the Iwate volcano and 6-7 wt.% beneath the Sannnome-gata volcano, respectively. Their arguments mean that primary melts beneath frontal-arc volcanoes and rear-arc volcanoes are both H2O-rich, yet there has been no direct evidence to support their arguments at the Sannnome-gata volcano because volcanic rocks are either almost aphyric and/or almost no melt inclusions were found. Hydrogen concentration in nominally anhydrous minerals serves as a hygrometer of arc basaltic melts (e.g., Hamada et al. 2013, Earth Planet. Sci. Lett.). In this study, hydrogen concentration of plagioclase as a crustal xenocryst was analyzed to estimate H2O concentration of basaltic melt coexisted with plagioclase before the eruption. Plagioclase xenocrists were separated from crushed scoria which erupted from the Sannome-gata volcano 20,000-24,000 years ago. Composition of the plagioclase core is homogeneous and ranges from An30 through An35. The rim is 150 to 200-μm-thick dusty zone whose composition is around An60, suggesting that the rim crystallized rapidly from degassed basaltic melt. The profiles of infrared absorption area per unit thickness across the plagioclase core were obtained using Fourier Transform InfraRed spectrometer (FTIR). The inner core contains hydrogen of about 60 wt. ppm H2O, and hydrogen concentration elevates at outer core. Hydrogen concentration at the outermost core of plagioclase is >200 wt. ppm H2O, suggesting that plagioclase xenocrists were taken by hydrous melt (H2O>5 wt.%; Hamada et al. 2014, Earth Planet. Sci. Lett.) and

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

    USGS Publications Warehouse

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

    1980-01-01

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

  4. Feldspar basalts in lunar soil and the nature of the lunar continents

    NASA Technical Reports Server (NTRS)

    Reid, A. M.; Ridley, W. I.; Harmon, R. S.; Warner, J.; Brett, R.; Jakes, P.; Brown, R. W.

    1974-01-01

    It is found that 25% on the Apollo-14 glasses have the same composition as the glasses in two samples taken from the Luna-16 column. The compositions are equivalent to feldspar basalt and anorthosite gabbro, and are similar to the feldspar basalts identified from Surveyor-7 analysis for lunar continents.

  5. Boron-bearing potassium feldspar of authigenic origin in closed-basin deposits

    USGS Publications Warehouse

    Sheppard, Richard A.; Gude, Arthur J.

    1973-01-01

    Silicic vitric tuffs in saline, alkaline lacustrine deposits are commonly altered to a variety of zeolites and potassium feldspar. The tuffs generally show a lateral gradation, in a basinward direction, of fresh glass to zeolites and then to potassium feldspar. Zeolites were formed early in diagenesis by reaction of the glass with the interstitial water. The feldspar, however, was formed later by reaction of the zeolites with interstitial water, and its formation can be correlated with water of relatively high salinity and alkalinity. Semiquantitative spectrographic analyses for boron in the zeolites and potassium feldspar show that most of the boron resides in the relatively late feldspar. The boron content of the zeolites is commonly less than 100 ppm, whereas the boron content of the potassium feldspar is commonly greater than 1,000 ppm. Boron apparently substitutes for aluminum in the feldspar structure and causes distortion of the monoclinic unit cell such that the b and c dimensions are shortened. These boron-bearing potassium feldspars having anomalous cell parameters seem unique to saline,alkaline lacustrine deposits and could serve as a prospecting aid for locating buried saline minerals.

  6. Evaluation of laboratory test method for determining the potential alkali contribution from aggregate and the ASR safety of the Three-Gorges dam concrete

    SciTech Connect

    Lu Duyou . E-mail: duyoulu@njut.edu.cn; Zhou, Xiaoling; Xu Zhongzi; Lan Xianghui; Tang Mingshu; Fournier, Benoit

    2006-06-15

    The releasable alkali from granite, which was used in the Three-Gorges concrete dam project in China, and from gneiss and feldspar was estimated by extraction in distilled water and super-saturated Ca(OH){sub 2} solution. Results show that: i) the finer the particles and the higher the temperature, the greater and faster the release of alkali; ii) compared with extraction by distilled water, super-saturated Ca(OH){sub 2} solution had a stronger activation on feldspar than on granite and gneiss; iii) for the three rocks tested, thermal activation had the largest effect on gneiss and a lower and similar effect on granite and feldspar. For very fine particles, temperature had a similar effect on the release of alkali by all three rocks. Because the aggregate used in the Three-Gorges dam concrete is non-reactive and a low calcium fly ash was used in the concrete, ASR would not be an issue for the dam, despite the release of alkali from the aggregate into the concrete.

  7. PROCESS OF RECOVERING ALKALI METALS

    DOEpatents

    Wolkoff, J.

    1961-08-15

    A process is described of recovering alkali metal vapor by sorption on activated alumina, activated carbon, dehydrated zeolite, activated magnesia, or Fuller's earth preheated above the vaporization temperature of the alkali metal and subsequent desorption by heating the solvent under vacuum. (AEC)

  8. [Study on crystal chemistry and spectra of feldspar from Zhoukoudian granodiorite].

    PubMed

    Zhang, Yong-wang; Zeng, Jian-hui; Liu, Yan; Guo, Jian-yu

    2009-09-01

    The chemical composition and spectra characteristic of feldspar from Zhoukoudian granodiorite were systematically analyzed. Based on the field work, some feldspar samples were selected for crystal chemistry and structure analysis through EMPA, IR, LRM and XRD. The compositions of the feldspar range between Ab (85.21) Or (0.18) An (9.11) and Ab (90.06) Or (3.00) An (13.27) by electronic microscope probe analysis. According to the XRD peak and its diffraction intensity, the mineral species was found the unit cell parameters were calculated. The absorption bands and peaks of infrared and Raman spectra were also assigned and the results show that the characteristics of its infrared and Raman spectra are in accordance with the ideal atlas of albite. The infrared spectra show that all the analyzed feldspar grains contain structural hydrogen, which occur as OH-. On the basis of the above analyses, the crystal chemistry and structure characteristics of feldspar were summarized.

  9. Purification of alkali metal nitrates

    DOEpatents

    Fiorucci, Louis C.; Gregory, Kevin M.

    1985-05-14

    A process is disclosed for removing heavy metal contaminants from impure alkali metal nitrates containing them. The process comprises mixing the impure nitrates with sufficient water to form a concentrated aqueous solution of the impure nitrates, adjusting the pH of the resulting solution to within the range of between about 2 and about 7, adding sufficient reducing agent to react with heavy metal contaminants within said solution, adjusting the pH of the solution containing reducing agent to effect precipitation of heavy metal impurities and separating the solid impurities from the resulting purified aqueous solution of alkali metal nitrates. The resulting purified solution of alkali metal nitrates may be heated to evaporate water therefrom to produce purified molten alkali metal nitrate suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of alkali metal nitrates.

  10. TEM observation of bacteria-induced plagioclase dissolution and secondary mineral formation

    NASA Astrophysics Data System (ADS)

    Tamura, T.; Kyono, A.; Nishimiya, Y.

    2015-12-01

    Silicate minerals are the most common minerals in the earth's crust. Bacteria are also distributed throughout the earth's surface environment. The silicate minerals are known to be dissolved by organic acids and polysaccharides known as bacteria metabolites. The metabolic activity of bacteria therefore plays an important role in the interaction between dissolution of the silicate minerals and formation of secondary minerals. However, little is known about the secondary mineral formation process associated with the bacterial metabolism. To clarify the bacterial effect on the mineral dissolution and the secondary mineral formation, we closely investigated the effect of bacterial activity on surface texture modification and chemical composition changes of plagioclase which is the most abundant silicate mineral in the earth's crust. The bacteria were isolated from soil and then added in a suitable medium with several plagioclase fragments (Ab100% and An100%). It was incubated for 10 days. Al and Si concentrations in the medium were measured by ICP-AES to monitor the dissolution of the plagioclase. Secondary mineral formation during the incubation was observed by TEM, EDS and SAED methods. The authors will give the experiment results and discuss the effect of bacterial activity on the plagioclase dissolution and the secondary mineral formation in detail.

  11. High-temperature hydrothermal alteration of tje Boehls Butte anorthosite: Origin of a bimodal plagioclase assemblage

    SciTech Connect

    Mora, Claudia I; Riciputi, Lee R; Cole, David; Walker, Karen

    2008-01-01

    The Boehls Butte anorthosite consists predominantly of an unusual bimodal assemblage of andesine and bytownite anorthite. Oxygen isotope compositions of the anorthosite were profoundly altered by high temperature, retrograde interaction with meteorichydrothermal fluids that varied in composition from isotopically evolved to nearly pristine meteoric water. Oxygen isotope ratios of bulk plagioclase separates are in the range ?7.0 to -6.2% V-SMOW, however, secondary ion mass spectrometry indicates spot-sized isotope values as low as -16%. Typical inter- and intra-plagioclase grain variability is 3 6%, and extreme heterogeneity of up to 20%is noted in a few samples. High-temperature hydrothermal alteration of intermediate plagioclase is proposed to explain the origin of bytownite anorthite in the anorthosite and creation of its unusual bimodal plagioclase assemblage. The anorthite-forming reaction created retrograde reaction-enhanced permeability which, together with rapid decompression, extension, and unroofing of the anorthosite complex, helped to accommodated influx of significant volumes of meteoric-hydrothermal fluids into the anorthosite.

  12. FeO and MgO in plagioclase of lunar anorthosites: Igneous or metamorphic?

    NASA Technical Reports Server (NTRS)

    Phinney, W. C.

    1994-01-01

    The combined evidence from terrestrial anorthosites and experimental laboratory studies strongly implies that lunar anorthosites have been subjected to high-grade metamorphic events that have erased the igneous signatures of FeO and MgO in their plagioclases. Arguments to the contrary have, to this point, been more hopeful than rigorous.

  13. Anomalous Plagioclase Compositions from Apollo 16 Impact Melts: Modification of Impact Melts on the Lunar Surface

    NASA Astrophysics Data System (ADS)

    Fagan, A.; Neal, C. R.

    2011-12-01

    A study of Apollo 16 impact melts has been initiated as part of the NASA Lunar Science Institute's Center for Lunar Science and Exploration. The investigation uses a novel approach to investigate the crystallization conditions for the igneous textured samples returned by Apollo 16. This approach uses a combination of crystal size distributions and mineral chemistry to develop a crystal stratigraphy approach to examine crystallization conditions. The Apollo 16 impact melts are enriched in Al2O3 (~25-28%) and are highly feldspathic with only minor amounts of pyroxene, olivine, and opaque minerals. Initial studies focused on sample 60635 where previous whole rock analyses show that, surprisingly this sample possesses a small negative Eu anomaly [1,2]. This is intriguing given the feldspathic nature of the sample (~70% modal plagioclase), which should impart a strong positive Eu anomaly on the whole rock signature. The major element compositions of the plagioclases are relatively homogeneous with a range of An94-98 and an average of An97.2. Plagioclase trace element compositions exhibit a much wider compositional range with some crystals having the predicted positive Eu anomaly but other showing an unexpected negative Eu anomaly. There are about the same number of crystals with a negative Eu anomaly as there are with a positive anomaly and both are equally distributed through the thin section (60635,2). Intriguingly, 5 plagioclase crystals from this sample contain both positive and negative Eu anomalies in different sections of the crystals. Subsequent analyses of other impact melt samples show that a further 4 samples from the LM/Station 10 site also contain plagioclase with both positive and negative Eu anomalies (60235,5; 60335,13; 60615,8; 60618,3 and ,4), along with one sample from Station 4 (64817,3). The hypothesis we are considering is that the impact melt(s) represented by these anomalous samples were generated by impact into typical lunar highlands materials

  14. Alkali metal and alkali earth metal gadolinium halide scintillators

    DOEpatents

    Bourret-Courchesne, Edith; Derenzo, Stephen E.; Parms, Shameka; Porter-Chapman, Yetta D.; Wiggins, Latoria K.

    2016-08-02

    The present invention provides for a composition comprising an inorganic scintillator comprising a gadolinium halide, optionally cerium-doped, having the formula A.sub.nGdX.sub.m:Ce; wherein A is nothing, an alkali metal, such as Li or Na, or an alkali earth metal, such as Ba; X is F, Br, Cl, or I; n is an integer from 1 to 2; m is an integer from 4 to 7; and the molar percent of cerium is 0% to 100%. The gadolinium halides or alkali earth metal gadolinium halides are scintillators and produce a bright luminescence upon irradiation by a suitable radiation.

  15. Alkali hydrolysis of trinitrotoluene.

    PubMed

    Karasch, Christian; Popovic, Milan; Qasim, Mohamed; Bajpai, Rakesh K

    2002-01-01

    Data for alkali hydrolysis of 2,4,6-trinitrotoluene (TNT) in aqueous solution at pH 12.0 under static (pH-controlled) as well as dynamic (pH-uncontrolled) conditions are reported. The experiments were conducted at two different molar ratios of TNT to hydroxyl ions at room temperature. The TNT disappeared rapidly from the solution as a first-order reaction. The complete disappearance of aromatic structure from the aqueous solution within 24 h was confirmed by the ultraviolet-visible (UV-VIS) spectra of the samples. Cuvet experiments in a UV-VIS spectrophotometer demonstrated the formation of Meisenheimer complex, which slowly disappeared via formation of aromatic compounds with fewer nitro groups. The known metabolites of TNT were found to accumulate only in very small quantities in the liquid phase.

  16. Giant plagioclase growth during storage of basaltic magma in Emeishan Large Igneous Province, SW China

    NASA Astrophysics Data System (ADS)

    Cheng, Li-Lu; Yang, Zong-Feng; Zeng, Ling; Wang, Yu; Luo, Zhao-Hua

    2014-02-01

    Giant plagioclase basalts (GPBs) reflect the storage of flood basalt magma in subvolcanic magma chambers at crustal depths. In this study of the Late Permian Emeishan large igneous province in southwest China, we focus on understanding the plumbing system and ascent of large-volume basaltic magma. We report a quantitative textural analysis and bulk-rock geochemical composition of clustered touching crystals (CT-type) and single isolated crystal (SI-type) GPB samples from 5- to 240-m-thick flows in the Daqiao section. Both types of GPBs are evolved (<6 MgO wt%), but have high Ti/Y ratios (>500) and high total FeO content (11.5-15.2 wt%). The mineral chemistry of the two types of plagioclase displays a small range of anorthite content (<5 mol%), which is consistent with their unzoned characteristics. The two types of GPBs have S-type crystal size distributions but have quite different slopes, intercepts, and characteristic lengths. The characteristic lengths of the five flows are 1.54, 2.99, 1.70, 3.22, and 1.86 mm, respectively. For plagioclase growth rates of 10-11 to 10-10 mm/s, steady-state magma chamber models with simple continuous crystal growth suggest that CT-type plagioclase megacrysts have the residence time of about 500-6,000 years, whereas the residence time for SI-type plagioclase is significantly longer, about 1,000-10,000 years. By combining field geology, quantitative textural data with geochemistry, we suggest that CT- and SI-type crystals grew and were coarsened in the outer part and inner part of a magma chamber, respectively. Magma evolution during storage is controlled by crystallization, crystal growth, and magma mixing, and pulsating eruptions occur in response to the continuous supply of hot magma.

  17. Dissolution rates and surface chemistry of feldspar glass and crystal. Final technical report, June 15, 1995 - August 14, 2001

    SciTech Connect

    Brantley, S.; Pantano, C.

    2002-06-11

    Final report summarizing the completed work of the project entitled 'Dissolution of Feldspar in the Field and Laboratory.' One of the highly debated questions today in low-temperature geochemical kinetics centers upon the rate and mechanism of dissolution of feldspar, the most common mineral in the crust. In this project, the mechanisms of feldspar dissolution were investigated by emphasizing experiments with feldspar glass and crystal while comparing surface and solution chemistry. Specifically, laboratory work focused on the structure of altered surface layers on feldspars, the rate of dissolution of feldspar crystal and glass, and the presence of porosity and surface coatings on feldspars. In a complementary field project, the use of Sr concentrations and isotopic ratios were used to calculate feldspar dissolution rates.

  18. Mixed alkali effect in nonconventional alkali gallotitanate glasses

    SciTech Connect

    Miyaji, Fumiaki; Hasegawa, Shinya; Yoko, Toshinobu; Sakka, Sumio . Inst. for Chemical Research)

    1993-02-01

    The mixed alkali effect on electrical conductivity, that is, the reduction of conductivity due to alkali mixing, was observed in Na[sub 2]O-K[sub 2]O-Ga[sub 2]O[sub 3]-TiO[sub 2] glasses, which are nonconventional in the sense that glass-forming oxides defined by Zachariasen are not involved. The magnitude of the reduction in conductivity of the present glasses due to alkali mixing was similar to that of corresponding mixed alkali silicate and phosphate glasses. The activation energy for electrical conduction showed a maximum around the composition Na/(Na + K) = 0.5, where the conductivity was at a minimum.

  19. Feldspar diagenesis in the Frio Formation, Brazoria County, Texas Gulf Coast

    SciTech Connect

    Land, L.S.; Milliken, K.L.

    1981-07-01

    Tremendous quantities of detrital feldspar have been dissolved or albitized below about 14000 ft (4267 m) in the Frio Formation (Oligocene), Chocolate Bayou Field, Brazoria County, Texas. Some sandstones no longer contain any unmodified detrital feldspar grains. Material transfer involved in these reactions is immense, affecting at least 15% of the rock volume. Thus, albitization has important implications for several other diagenetic processes that involve feldspars or their components. These processes include formation of secondary porosity, precipitation of quartz and carbonate cements, and the evolution of Na-Ca-Cl formation water.

  20. Upgrading platform using alkali metals

    SciTech Connect

    Gordon, John Howard

    2014-09-09

    A process for removing sulfur, nitrogen or metals from an oil feedstock (such as heavy oil, bitumen, shale oil, etc.) The method involves reacting the oil feedstock with an alkali metal and a radical capping substance. The alkali metal reacts with the metal, sulfur or nitrogen content to form one or more inorganic products and the radical capping substance reacts with the carbon and hydrogen content to form a hydrocarbon phase. The inorganic products may then be separated out from the hydrocarbon phase.

  1. Feldspar-Bearing Igneous Rocks at Gale: A ChemCam Campaign

    NASA Astrophysics Data System (ADS)

    Sautter, V.; Fabre, C.; Toplis, M.; Wiens, R. C.; Gasnault, O.; Forni, O.; Mangold, N.

    2014-09-01

    We present the first in situ evidences of feldspar-rich rocks ranging from granodioritic and alkalin effusive rocks (trachy basalts and syenitic liquids). Implication for primitive noachain crust will be discussed.

  2. Authigenic potassium feldspar in Cambrian carbonates: Evidence of Alleghanian brine migration

    USGS Publications Warehouse

    Hearn, P.P.; Sutter, J.F.

    1985-01-01

    The shallow-water limestones and dolostones of the Conococheague Limestone (Upper Cambrian) of western Maryland contain large amounts of authigenic potassium feldspar. The presence of halite daughter crystals in breached fluid inclusions, low whole-rock ratios of chlorine to bromine, and thermochemical data suggest that the potassium feldspar formed at low temperature by the reaction of connate brines with intercalated siliciclastic debris. Analyses of argon age spectra indicate that the authigenic feldspar probably formed during Late Pennsylvanian to Early Permian time. These results may indicate mobilization and migration of connate brines brought about by Alleghanian folding. The widespread occurrence of authigenic potassium feldspar in Cambrian and Ordovician carbonate rocks throughout the Appalachians suggests that this may have occurred throughout the entire basin.

  3. Clouding of pyroxene and plagioclase in eucrites - Implications for post-crystallization processing

    NASA Technical Reports Server (NTRS)

    Harlow, G. E.; Klimentidis, R.

    1980-01-01

    The clouding of pyroxene and plagioclase in the basaltic eucrites ALHA 77302, Juvinas, Pasamonte, and Stannern, is caused by finely disseminated inclusions. This clouding is interpreted to be the result of exsolution of minor components which became incompatible and crystallized on microfractures and other nucleation sites during postbrecciation metamorphism. The phases found in clouding require reduction of silicate FeO to metallic Fe in both pyroxene and plagioclase and possible redox of Cr(2+) to Cr(3+) in pyroxene. The assemblage of coexisting phases that make up clouding record conditions of T approximately equal to 900 C and f(O2) of 10 to the -16th to 10 to the -18th during slow cooling. Thus, clouding can be a useful indicator of postcrystallization conditions.

  4. Orthopyroxene-plagioclase fragments in the lunar soil from apollo 12.

    PubMed

    Fuchs, L H

    1970-08-28

    Rock fragments consisting of orthopyroxene-calcic plagioclase assemblages appear to be more common in Apollo 12 soil samples than in the breccias or soil from Apollo 11 and are mineralogically and chemically different from any of the crystalline rocks returned by either Apollo 11 or Apollo 12. Compositionally, these fragments are orthopyroxenites and feldspathic orthopyroxenites. They are probably not fragments of meteorites; other considerations point to a near-surface lunar origin.

  5. Plagioclase nucleation and growth kinetics in a hydrous basaltic melt by decompression experiments

    NASA Astrophysics Data System (ADS)

    Arzilli, Fabio; Agostini, C.; Landi, P.; Fortunati, A.; Mancini, L.; Carroll, M. R.

    2015-12-01

    Isothermal single-step decompression experiments (at temperature of 1075 °C and pressure between 5 and 50 MPa) were used to study the crystallization kinetics of plagioclase in hydrous high-K basaltic melts as a function of pressure, effective undercooling (Δ T eff) and time. Single-step decompression causes water exsolution and a consequent increase in the plagioclase liquidus, thus imposing an effective undercooling (∆ T eff), accompanied by increased melt viscosity. Here, we show that the decompression process acts directly on viscosity and thermodynamic energy barriers (such as interfacial-free energy), controlling the nucleation process and favoring the formation of homogeneous nuclei also at high pressure (low effective undercoolings). In fact, this study shows that similar crystal number densities ( N a) can be obtained both at low and high pressure (between 5 and 50 MPa), whereas crystal growth processes are favored at low pressures (5-10 MPa). The main evidence of this study is that the crystallization of plagioclase in decompressed high-K basalts is more rapid than that in rhyolitic melts on similar timescales. The onset of the crystallization process during experiments was characterized by an initial nucleation event within the first hour of the experiment, which produced the largest amount of plagioclase. This nucleation event, at short experimental duration, can produce a dramatic change in crystal number density ( N a) and crystal fraction ( ϕ), triggering a significant textural evolution in only 1 h. In natural systems, this may affect the magma rheology and eruptive dynamics on very short time scales.

  6. [Study on the fine structure of K-feldspar of Qichun granite].

    PubMed

    Du, Deng-Wen; Hong, Han-Lie; Fan, Kan; Wang, Chao-Wen; Yin, Ke

    2013-03-01

    Fine structure of K-feldspar from the Qichun granite was investigated using X-ray diffraction (XRD), Fourier infrared absorption spectroscopy (FTIR), and inductively coupled plasma mass spectrometry methods to understand the evolution of the granitic magmatism and its correlation to molybdenite mineralization. The XRD results showed that K-feldspar of the potassic alteration veins has higher ordering index and triclinicity and is namely microcline with triclinic symmetry. K-feldspar of the early cretaceous granite has relatively lower ordering index and has widening [131] peak and is locally triclinic ordering. K-feldspar of the late cretaceous granite has lowest ordering index and sharp [131] peak and is honiogeneously monoclinic. The FTIR results showed that the IR spectra of the Qichun K-feldspar are similar to that of orthoclase reported by Farmer (1974). The 640 cm-1 absorption band increases while the 540 cm-' absorption band decreases with increase in K-feldspar ordering index, also, the 1,010 cm-1 absorption band separates into 1,010 and 1,046 cm-1 absorption bands, with a change in the band shape from widening to sharp outline. The ICP-MS results suggested that K-feldspar of the early cretaceous granite has relatively higher metal elements and rare earth elements, and the granite exhibits better mineralization background, K-feldspar of the potassic alteration veins has markedly lower Sr and Ba, indicating that the alteration fluid originated from the granitic magmatism, and hence, potassic alteration is a good indicator for molybdenite exploration. PMID:23705418

  7. [Study on the fine structure of K-feldspar of Qichun granite].

    PubMed

    Du, Deng-Wen; Hong, Han-Lie; Fan, Kan; Wang, Chao-Wen; Yin, Ke

    2013-03-01

    Fine structure of K-feldspar from the Qichun granite was investigated using X-ray diffraction (XRD), Fourier infrared absorption spectroscopy (FTIR), and inductively coupled plasma mass spectrometry methods to understand the evolution of the granitic magmatism and its correlation to molybdenite mineralization. The XRD results showed that K-feldspar of the potassic alteration veins has higher ordering index and triclinicity and is namely microcline with triclinic symmetry. K-feldspar of the early cretaceous granite has relatively lower ordering index and has widening [131] peak and is locally triclinic ordering. K-feldspar of the late cretaceous granite has lowest ordering index and sharp [131] peak and is honiogeneously monoclinic. The FTIR results showed that the IR spectra of the Qichun K-feldspar are similar to that of orthoclase reported by Farmer (1974). The 640 cm-1 absorption band increases while the 540 cm-' absorption band decreases with increase in K-feldspar ordering index, also, the 1,010 cm-1 absorption band separates into 1,010 and 1,046 cm-1 absorption bands, with a change in the band shape from widening to sharp outline. The ICP-MS results suggested that K-feldspar of the early cretaceous granite has relatively higher metal elements and rare earth elements, and the granite exhibits better mineralization background, K-feldspar of the potassic alteration veins has markedly lower Sr and Ba, indicating that the alteration fluid originated from the granitic magmatism, and hence, potassic alteration is a good indicator for molybdenite exploration.

  8. Evidence for Coordination and Redox Changes of Iron in Shocked Feldspar from Synchrotron MicroXANES

    NASA Technical Reports Server (NTRS)

    Delaney, J. S.; Dyar, M. D.; Hoerz, F.; Johnson, J. R.

    2003-01-01

    Shock modification of feldspar has been documented and experimentally reproduced in many studies since the recognition of maskelynite in Shergotty. Experimentally shocked feldspar samples have been well studied using chemical and crystallographic techniques. The crystallographic, site-specific characterization of major and minor elements is less well documented. We present early x-ray absorption (XAS) spectral data for a suite of albitite samples that were experimentally shocked at pressures between 17 and 50 Gpa.

  9. Recycled oceanic crust observed in 'ghost plagioclase' within the source of Mauna Loa lavas

    PubMed

    Sobolev; Hofmann; Nikogosian

    2000-04-27

    The hypothesis that mantle plumes contain recycled oceanic crust is now widely accepted. Some specific source components of the Hawaiian plume have been inferred to represent recycled oceanic basalts, pelagic sediments or oceanic gabbros. Bulk lava compositions, however, retain the specific trace-element fingerprint of the original crustal component in only a highly attenuated form. Here we report the discovery of exotic, strontium-enriched melt inclusions in Mauna Loa olivines. Their complete trace-element patterns strongly resemble those of layered gabbros found in ophiolites, which are characterized by cumulus plagioclase with very high strontium abundances. The major-element compositions of these melts indicate that their composition cannot be the result of the assimilation of present-day oceanic crust through which the melts have travelled. Instead, the gabbro has been transformed into a (high-pressure) eclogite by subduction and recycling, and this eclogite has then been incorporated into the Hawaiian mantle plume. The trace-element signature of the original plagioclase is present only as a 'ghost' signature, which permits specific identification of the recycled rock type. The 'ghost plagioclase' trace-element signature demonstrates that the former gabbro can retain much of its original chemical identity through the convective cycle without completely mixing with other portions of the former oceanic crust.

  10. Recycled oceanic crust observed in 'ghost plagioclase' within the source of Mauna Loa lavas

    PubMed

    Sobolev; Hofmann; Nikogosian

    2000-04-27

    The hypothesis that mantle plumes contain recycled oceanic crust is now widely accepted. Some specific source components of the Hawaiian plume have been inferred to represent recycled oceanic basalts, pelagic sediments or oceanic gabbros. Bulk lava compositions, however, retain the specific trace-element fingerprint of the original crustal component in only a highly attenuated form. Here we report the discovery of exotic, strontium-enriched melt inclusions in Mauna Loa olivines. Their complete trace-element patterns strongly resemble those of layered gabbros found in ophiolites, which are characterized by cumulus plagioclase with very high strontium abundances. The major-element compositions of these melts indicate that their composition cannot be the result of the assimilation of present-day oceanic crust through which the melts have travelled. Instead, the gabbro has been transformed into a (high-pressure) eclogite by subduction and recycling, and this eclogite has then been incorporated into the Hawaiian mantle plume. The trace-element signature of the original plagioclase is present only as a 'ghost' signature, which permits specific identification of the recycled rock type. The 'ghost plagioclase' trace-element signature demonstrates that the former gabbro can retain much of its original chemical identity through the convective cycle without completely mixing with other portions of the former oceanic crust. PMID:10801125

  11. A Plagioclase-Olivine-Spinel-Magnetite Inclusion from Maralinga (CK): A Record of Sequential Condensation

    NASA Astrophysics Data System (ADS)

    Zinner, E.; Brandstatter, F.; Kurat, G.

    1995-09-01

    An unusual inclusion of triangular cross section (5 mm x 2.5 mm in size) from the Maralinga CK chondrite has a zonal structure, consisting of core, mantle, and crust. The core (2.5 x 1 mm) consists mainly of plagioclase-olivine intergrowth (troctolite) with ophitic texture, but also contains minor clinopyroxene and Cl-apatite, as well as some calcite, which partially fills pore space. The mantle varies in thickness (0.1-1.5 mm) and consists of a dense intergrowth of green spinel and plagioclase with abundant dispersed magnetite grains of widely varying sizes (1-100 micrometer) and shapes. The spinel-plagioclase intergrowth has, in places, symplectitic texture and variable plag/sp ratios and grain-sizes. The mantle is frequently cut by plagioclase-rich veins connecting the core with the crust. Minor phases in the mantle are ilmenite (exsolution lamellae in magnetite) and calcite (in rare pore space). The thin (^about10 micrometer) discontinuous crust consists mainly of plagioclase with some olivine and magnetite and is commonly intimately intergrown with the chondrite matrix. An indentation contains an olivine-plagioclase intergrowth with subophitic texture in places. A super-crust of calcite almost continuously covers the inclusion. Phase compositions, as determined by EMP, are: Olivine - Fa = 33.1, NiO = 0.62 wt%, plagioclase - An 55-74 with high-An compositions in the mantle, clinopyroxene - Fs 10, Wo 46.7, spinel - Fe/Fe+Mg = 0.55, NiO = 1.53 wt%, and magnetite - TiO2 = 0.50 wt%, NiO = 0.57 wt%. Abundances of up to 37 trace elements were determined by secondary ion mass spectrometry[1]. Most phases are rich in trace elements and have group II REE patterns[2] with depletions of the refractory HREEs, a strong positive Tm anomaly and, commonly, a negative Eu anomaly. The exceptions are olivine, which has LREE depletions relative to the HREEs, and calcite, which does not show any significant REE fractionation at the 1xCI abundance level. Thus, trace element

  12. The dissolution of naturally weathered feldspar and quartz

    NASA Astrophysics Data System (ADS)

    Anbeek, Chris; Van Breemen, Nico; Meijer, Edward L.; Van Der Plas, Leendert

    1994-11-01

    Surface area measurements and dissolution experiments were performed on subsamples from a naturally weathered mineral assemblage (100-1000 μm) consisting of feldspar and quartz. The subsamples were obtained by splitting the assemblage into four different ranges of grain density, each of which was sieved to three different size fractions. BET-krypton and geometric surface areas, combined with mineralogical data and average grain diameters, showed that (1) surface roughness factors of the subsamples are generally much higher than those of freshly created surfaces by grinding and (2) for individual density ranges (i.e., at constant mineralogical composition), the surface roughness factor decreases linearly with decreasing grain diameter. Scanning electron microscopy and X-Ray diffraction showed that contributions to the surface roughness factors from secondary mineral coatings, macropores (diameters >50 nm) and etch pits are insignificant. In contrast, krypton adsorption data indicated that by far most surface roughness is due to the presence of micropores and mesopores (diameters <50 nm). These findings strongly suggest that, during natural weathering, micropores/mesopores develop at sites whose density (cm -2 of geometric surface area) is approximately proportional to grain diameter. Multivariate linear regression showed that, at similar grain diameters, the micropore/mesopore density increases in the order: quartz < microcline < albite < oligoclase/andesine. This sequence is similar to the well-known sequence of relative weatherability of these minerals, suggesting a relationship between weatherability and micropore/mesopore density. At pH 3 HCl and ambient temperature, dissolution rates of Na, K, Ca, Al and Si from the subsamples normalized to the BET-krypton surface area, were essentially independent of the grain diameter. Due to effects from surface roughness, dissolution rates normalized to the geometric surface area were essentially proportional to grain

  13. Alkalis in Coal and Coal Cleaning Products / Alkalia W Węglu I Productach Jego Wzbogacania

    NASA Astrophysics Data System (ADS)

    Bytnar, Krzysztof; Burmistrz, Piotr

    2013-09-01

    In the coking process, the prevailing part of the alkalis contained in the coal charge goes to coke. The content of alkalis in coal (and also in coke) is determined mainly by the content of two elements: sodium and potasium. The presence of these elements in coal is connected with their occurrence in the mineral matter and moisture of coal. In the mineral matter and moisture of the coals used for the coke production determinable the content of sodium is 26.6 up to 62. per cent, whereas that of potassium is 37.1 up to 73.4 per cent of the total content of alkalis. Major carriers of alkalis are clay minerals. Occasionally alkalis are found in micas and feldspars. The fraction of alkalis contained in the moisture of the coal used for the production of coke in the total amount of alkalis contained there is 17.8 up to 62.0 per cent. The presence of sodium and potassium in the coal moisture is strictly connected with the presence of the chloride ions. The analysis of the water drained during process of the water-extracting from the flotoconcentrate showed that the Na to K mass ratio in the coal moisture is 20:1. Increased amount of the alkalis in the coal blends results in increased content of the alkalis in coke. This leads to the increase of the reactivity (CRI index), and to the decrease of strength (CSR index) determined with the Nippon Steel Co. method. W procesie koksowania przeważająca część zawartych we wsadzie węglowym alkaliów przechodzi do koksu. Zawartość alkaliów w węglu, a co za tym idzie i w koksie determinowana jest głównie zawartością dwóch pierwiastków: sodu i potasu. Obecność tych pierwiastków w węglu wiąże się z występowaniem ich w substancji mineralnej i wilgoci węgla. W substancji mineralnej oraz wilgoci węgli stosowanych do produkcji koksu, oznaczona zawartość sodu wynosi od 26.6 do 62.9%, a zawartość potasu od 37.1 do 73.4% alkaliów ogółem. Głównymi nośnikami alkaliów w substancji mineralnej są minera

  14. Experimental studies of alunite: II. Rates of alunite-water alkali and isotope exchange

    USGS Publications Warehouse

    Stoffregen, R.E.; Rye, R.O.; Wasserman, M.D.

    1994-01-01

    Rates of alkali exchange between alunite and water have been measured in hydrothermal experiments of 1 hour to 259 days duration at 150 to 400??C. Examination of run products by scanning electron microscope indicates that the reaction takes place by dissolution-reprecipitation. This exchange is modeled with an empirical rate equation which assumes a linear decrease in mineral surface area with percent exchange (f) and a linear dependence of the rate on the square root of the affinity for the alkali exchange reaction. This equation provides a good fit of the experimental data for f = 17% to 90% and yields log rate constants which range from -6.25 moles alkali m-2s-1 at 400??C to - 11.7 moles alkali m-2s-1 at 200??C. The variation in these rates with temperature is given by the equation log k* = -8.17(1000/T(K)) + 5.54 (r2 = 0.987) which yields an activation energy of 37.4 ?? 1.5 kcal/mol. For comparison, data from O'Neil and Taylor (1967) and Merigoux (1968) modeled with a pseudo-second-order rate expression give an activation energy of 36.1 ?? 2.9 kcal/mol for alkali-feldspar water Na-K exchange. In the absence of coupled alkali exchange, oxygen isotope exchange between alunite and water also occurs by dissolution-reprecipitation but rates are one to three orders of magnitude lower than those for alkali exchange. In fine-grained alunites, significant D-H exchange occurs by hydrogen diffusion at temperatures as low as 100??C. Computed hydrogen diffusion coefficients range from -15.7 to -17.3 cm2s-1 and suggest that the activation energy for hydrogen diffusion may be as low as 6 kcal/mol. These experiments indicate that rates of alkali exchange in the relatively coarse-grained alunites typical of hydrothermal ore deposits are insignificant, and support the reliability of K-Ar age data from such samples. However, the fine-grained alunites typical of low temperature settings may be susceptible to limited alkali exchange at surficial conditions which could cause

  15. Monoclinic and Tetragonal Plagioclase (An54) in Shock Veins from the Central Uplift of the Manicouagan Impact Structure

    NASA Astrophysics Data System (ADS)

    Spray, J. G.; Boonsue, S.

    2016-08-01

    This work documents the discovery of monoclinic- and tetragonal-structured plagioclase. Critically, the high-pressure polymorphs possess the same composition as the non-shocked triclinic phase (An54).

  16. Water in Olivine, Clinopyroxenen and Plagioclase of Lunar Meteorites of the NWA 773 Clan by IR Micro-Spectrosocpy

    NASA Astrophysics Data System (ADS)

    Kayama, M.; Nakashima, S.; Tomioka, N.; Ohtani, E.; Seto, Y.; Nagaoka, H.; Ozawa, S.; Sekine, T.; Miyahara, M.; Miyake, A.; Götze, J.; Tomeoka, K.

    2016-08-01

    Water in olivine, clinopyroxene and plagioclase of gabbroic lunar meteorites of Northwest Africa 2977 and 6950 and gabbroic/basaltic brecciated lunar meteorite of NWA 2727 were characterized by in-situ Fourier-transform infrared micro-spectroscopy.

  17. Hydrothermal alkali metal catalyst recovery process

    DOEpatents

    Eakman, James M.; Clavenna, LeRoy R.

    1979-01-01

    In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles primarily in the form of water soluble alkali metal formates by treating the particles with a calcium or magnesium-containing compound in the presence of water at a temperature between about 250.degree. F. and about 700.degree. F. and in the presence of added carbon monoxide. During the treating process the water insoluble alkali metal compounds comprising the insoluble alkali metal residues are converted into water soluble alkali metal formates. The resultant aqueous solution containing water soluble alkali metal formates is then separated from the treated particles and any insoluble materials formed during the treatment process, and recycled to the gasification process where the alkali metal formates serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. This process permits increased recovery of alkali metal constituents, thereby decreasing the overall cost of the gasification process by reducing the amount of makeup alkali metal compounds necessary.

  18. Nature and origin of authigenic K-feldspar in Precambrian basement rocks of the North American midcontinent

    SciTech Connect

    Duffin, M.E. )

    1989-08-01

    Authigenic K-feldspar occurs in alteration profiles in uppermost Precambrian igneous and metamorphic basement rocks of the midcontinent. The K-feldspar is widespread and has been identified in six states. The profiles occur directly below the Cambrian-Precambrian unconformity and range from about <1 to 8 m in thickness. Authigenic K-feldspar occurs throughout the profile. The K-feldspar is monoclinic or triclinic by X-ray diffraction, of end-member composition, and may compose 63% of rock volume. Much of the K-feldspar formed by replacement of primary feldspar. A sample of wholly authigenic K-feldspar from altered basement in southern Illinois gives a K/Ar data of 549 {plus minus} 18 Ma (Early Cambrian). This data is in agreement with Early Cambrian Rb/Sr dates for potassic alteration of uppermost Precambrian basement in Ohio. Dated authigenic K-feldspars from both Ohio and Illinois give identical {delta}{sup 18}O values of 17.5, suggesting formation from a very similar fluid. Concordancy of both dates and {delta}{sup 18}O values suggests that the K-feldspar formed during an episode of potassic alteration during Early Cambrian time that affected much of midcontinent North America. The dates and {delta}{sup 18}O values for K-feldspar, when considered together, do not fit any of the hypotheses presented here.

  19. Massive Red-Staining and Albitization of Feldspars in Paleozoic Basement Rocks of Western Europe and Their Association with the Triassic Palaeogeography

    NASA Astrophysics Data System (ADS)

    Fabrega, C.; Parcerisa, D.; Franke, C.; Thiry, M.; Yao, K.; Gómez-Gras, D.

    2013-12-01

    Albitization of feldspars is a widespread mineral replacement process of the upper crust. An ubiquitous and pervasive red-staining albitization of feldspars has been observed in the feldspathic rocks of the Variscan basement in the Sudetes, Armorican, Morvan, Roc de Frausa and Montseny-Guilleries Massifs (Western Europe). These crystalline massifs were strongly eroded during Permian and Triassic times and suffered a long-lasting exposition in the Permian-Triassic palaeosurface. The albitized rocks contain minute Fe-oxides hoisted within the microporosity of the secondary albite. The intimate textural relationship between the Fe-oxides and the albite strongly suggest that they are coetaneous with albitization. The microscope, cathodoluminescence, SEM and EMPA analyses reveal that almost all plagioclases and some K-feldspars are albitized in those areas close to the Permian-Triassic palaeosurface. Moving downwards the palaeosurface the albitization of Variscan rocks progressively disappears. Field mapping of the albitized areas points to estimated thickness about 100-200m. In the uppermost parts of the profile almost all plagioclases are totally albitized and the rock shows a strong and pervasive reddening, whereas in the lowermost parts the mineral replacement is restricted to fractures and neighbouring walls and the rock in tinted with a soft pink colour. These observations suggest that albitization is linked to that palaeosurface and constitutes a paleoalteration profile beneath the Permian-Triassic palaeosurface. All these observations suggest that the mineral replacement could have been driven by descending Na+ rich brines related with or coming from the Permian-Triassic palaeosurface. Ricodel et al. (2007) determined a Triassic age for the paleomagnetic signature of the Fe-oxides hoisted within the microporosity of albite in the Morvan Massif. The narrow textural relationship between the Fe-oxides and the albite support the idea that this is the age of

  20. Three Magmatic Components in the 1973 Eruption of Eldfell Volcano, Iceland: Evidence From Plagioclase Crystal Size Distribution (CSD) and Geochemistry

    NASA Astrophysics Data System (ADS)

    Higgins, M. D.; Roberge, J.

    2006-12-01

    The 1973 eruption of Eldfell volcano, Iceland, appears to have been a short, simple event, but textural and geochemical evidence suggest that it may have had three different magmatic components. The first-erupted fissure magmas were chemically evolved, rich in plagioclase (~18%) and had shallow, straight crystal size distribution (CSD) curves. The early lavas were less evolved chemically, had lower plagioclase contents (~13%) and steeper, slightly concave up CSDs. The late lavas were chemically similar to the early lavas, but even richer in plagioclase than the initial magmas (~24%) and had the steepest CSDs. There is no chemical evidence for plagioclase fractionation, but compositional diversity could be produced by clinopyroxene fractionation which must have occurred at depth. We propose that the eruption started with old, coarsened (Ostwald ripened) magma left over from a previous eruption, possibly that which produced Surtsey Island ten years earlier. The early flows are mixtures of small amounts of this old magma with a new, low crystallinity, uncoarsened magma. The late flows are yet another new magma from depth, chemically similar to the early flows, but which has grown plagioclase under increasing saturation (undercooling) perhaps during ascent to a higher level staging chamber. All three magmatic components may have originated from the same parent, but had varying degrees of clinopyroxene fractionation, plagioclase nucleation and growth, and coarsening. Eichelberger et al. (2006) have suggested that compositional diversity in arc volcanoes reflects mixing of independently evolved magma batches. Perhaps the same also occurs in other settings.

  1. Three magmatic components in the 1973 eruption of Eldfell volcano, Iceland: Evidence from plagioclase crystal size distribution (CSD) and geochemistry

    NASA Astrophysics Data System (ADS)

    Higgins, Michael D.; Roberge, Julie

    2007-03-01

    The 1973 eruption of Eldfell volcano, Iceland, appears to have been a short, simple event, but textural and geochemical evidence suggest that it may have had three different magmatic components. The first-erupted fissure magmas were chemically evolved, rich in plagioclase (˜ 18%) and had shallow, straight crystal size distribution (CSD) curves. The early lavas were less evolved chemically, had lower plagioclase contents (˜ 13%) and steeper, slightly concave up CSDs. The late lavas were chemically similar to the early lavas, but even richer in plagioclase than the initial magmas (˜ 24%) and had the steepest CSDs. There was no chemical evidence for plagioclase fractionation, but compositional diversity could be produced by clinopyroxene fractionation which must have occurred at depth. We propose that the eruption started with old, coarsened (Ostwald ripened) magma left over from a previous eruption, possibly that which produced Surtsey Island ten years earlier. The early flows may be mixtures of small amounts of this old magma with a new, low crystallinity, uncoarsened magma or a completely new magma. The late flows are another new magma from depth, chemically similar to the early flows, but which has grown plagioclase under increasing saturation (undercooling) perhaps during its ascent. All three magmatic components may have originated from the same parent, but had varying degrees of clinopyroxene fractionation, plagioclase nucleation and growth, and coarsening.

  2. Origin of biotite-hornblende-garnet coronas between oxides and plagioclase in olivine metagabbros, Adirondack region, New York

    USGS Publications Warehouse

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

    1982-01-01

    Complex multivariant reactions involving Fe-Ti oxide minerals, plagioclase and olivine have produced coronas of biotite, hornblende and garnet between ilmenite and plagioclase in Adirondack olivine metagabbros. Both the biotite (6-10% TiO2) and the hornblende (3-6% TiO2) are exceptionally Titanium-rich. The garnet is nearly identical in composition to the garnet in coronas around olivine in the same rocks. The coronas form in two stages: (a) Plagioclase+Fe-Ti Oxides+Olivine+water =Hornblende+Spinel+Orthopyroxene??Biotite +more-sodic Plagioclase (b) Hornblende+Orthopyroxene??Spinel+Plagioclase =Garnet+Clinopyroxene+more-sodic Plagioclase The Orthopyroxene and part of the clinopyroxene form adjacent to olivine. Both reactions are linked by exchange of Mg2+ and Fe2+ with the reactions forming pyroxene and garnet coronas around olivine in the same rocks. The reactions occur under granulite fades metamorphic conditions, either during isobaric cooling or with increasing pressure at high temperature. ?? 1983 Springer-Verlag.

  3. A shock-metamorphic model for silicate darkening and compositionally variable plagioclase in CK and ordinary chondrites

    SciTech Connect

    Rubin, A.E. )

    1992-04-01

    Silicate darkening in ordinary chondrites (OC) is caused by tiny grains of metallic Fe-Ni and troilite occurring mainly within curvilinear trails that traverse silicate interiors and decorate or, in some cases, cut across silicate grain boundaries. Highly shocked OC tend to have greater degrees of silicate darkening than lightly shocked OC; this indicates that silicate darkening is probably a result of shock metamorphism. The low Fe-FeS eutectic temperature (988C) renders metal and troilite susceptible to melting and mobilization during shock heating. Unshocked OC tend to have plagioclase with uniform compositions; shocked OC tend to have plagioclase with more variable (albeit still stoichiometric) compositions. The low impedance of plagioclase to shock compression makes it particularly susceptible to melting and mobilization; this is consistent with the molten appearance of plagioclase in highly shocked OC (e.g., Rose City and Paragould). CK chondrites also have compositionally variable plagioclase. The common association of silicate darkening with compositionally variable plagioclase is consistent with the hypothesis that both are products of shock metamorphism. Some CK and OC chondrites exhibit light shock effects in olivine that are consistent with equilibrium peak shock pressures that are too low to account for the silicate darkening or opaque shock veins in these meteorites. Therefore, the olivine in these chondrites may have been annealed after intense shock produced these effects. A few CK chondrites that contain olivine with undulose or mosaic extinction (e.g., LEW87009 and EET83311) may have been shocked again, after annealing.

  4. Laser Ablation Analyses of Pb Isotopes in Ancient Feldspars: Application to a Polymetamorphic Terrane, West Greenland

    NASA Astrophysics Data System (ADS)

    Krogstad, E. J.; Baker, J. A.; Waight, T. E.

    2001-12-01

    Laser ablation was used to sample the Pb isotopic compositions of various feldspars, as well as isotopic standards. The ablated material was analyzed by MC-ICP-MS. The resulting accuracy and external precision are comparable to conventional (i.e., not double or triple-spiked) feldspar Pb isotope analyses done by TIMS. However, the data can be acquired with no chemical separation and require only a few minutes per sample. A pilot study was made of the feldspars from a polymetamorphic terrane in West Greenland, in which Late Archean gneisses were deformed and metamorphosed during the Early Proterozoic. In this terrane, isotopic contrasts have long been sought to delineate any suture between discrete Archean continental blocks that might mark the site of ocean closure. Previous whole rock Nd and Pb isotopic studies had yielded equivocal results on the presence of such an isotopic discontinuity. The laser ablation feldspar data presented here, combined with existing whole rock Pb data, point to real differences in the sources of gneisses from various parts of the orogen. This indicates that the laser ablation method of sampling feldspar Pb holds real potential for future reconnaissance studies of old continental crust in a manner similar to that of zircon U-Pb geochronology studies.

  5. Progressive deformation of feldspar recording low-barometry impact processes, Tenoumer impact structure, Mauritania

    NASA Astrophysics Data System (ADS)

    Jaret, Steven J.; Kah, Linda C.; Harris, R. Scott

    2014-06-01

    The Tenoumer impact structure is a small, well-preserved crater within Archean to Paleoproterozoic amphibolite, gneiss, and granite of the Reguibat Shield, north-central Mauritania. The structure is surrounded by a thin ejecta blanket of crystalline blocks (granitic gneiss, granite, and amphibolite) and impact-melt rocks. Evidence of shock metamorphism of quartz, most notably planar deformation features (PDFs), occurs exclusively in granitic clasts entrained within small bodies of polymict, glass-rich breccia. Impact-related deformation features in oligoclase and microcline grains, on the other hand, occur both within clasts in melt-breccia deposits, where they co-occur with quartz PDFs, and also within melt-free crystalline ejecta, in the absence of co-occurring quartz PDFs. Feldspar deformation features include multiple orientations of PDFs, enhanced optical relief of grain components, selective disordering of alternate twins, inclined lamellae within alternate twins, and combinations of these individual textures. The distribution of shock features in quartz and feldspar suggests that deformation textures within feldspar can record a wide range of average pressures, starting below that required for shock deformation of quartz. We suggest that experimental analysis of feldspar behavior, combined with detailed mapping of shock metamorphism of feldspar in natural systems, may provide critical data to constrain energy dissipation within impact regimes that experienced low average shock pressures.

  6. Asbestos contamination in feldspar extraction sites: a failure of prevention? Commentary.

    PubMed

    Cavariani, Fulvio

    2016-01-01

    Fibrous tremolite is a mineral species belonging to the amphibole group. It is present almost everywhere in the world as a natural contaminant of other minerals, like talc and vermiculite. It can be also found as a natural contaminant of the chrysotile form of asbestos. Tremolite asbestos exposures result in respiratory health consequences similar to the other forms of asbestos exposure, including lung cancer and mesothelioma. Although abundantly distributed on the earth's surface, tremolite is only rarely present in significant deposits and it has had little commercial use. Significant presence of amphibole asbestos fibers, characterized as tremolite, was identified in mineral powders coming from the milling of feldspar rocks extracted from a Sardinian mining site (Italy). This evidence raises several problems, in particular the prevention of carcinogenic risks for the workers. Feldspar is widespread all over the world and every year it is produced in large quantities and it is used for several productive processes in many manufacturing industries (over 21 million tons of feldspar mined and marketed every year). Until now the presence of tremolite asbestos in feldspar has not been described, nor has the possibility of such a health hazard for workers involved in mining, milling and handling of rocks from feldspar ores been appreciated. Therefore the need for a wider dissemination of knowledge of these problems among professionals, in particular mineralogists and industrial hygienists, must be emphasized. In fact both disciplines are necessary to plan appropriate environmental controls and adequate protections in order to achieve safe working conditions. PMID:27033611

  7. Evolution of the lunar crust: SIMS study of plagioclase from ferroan anorthosites

    SciTech Connect

    Papike, J.J.; Fowler, G.W.; Shearer, C.K.

    1997-06-01

    The lunar crust, down to a depth of {approximately}65 km, is composed of older (>4.5 Ga) ferroan anorthosites and younger (4.43-4.17 Ga) Mg-suite lithologies which include dunites, troctolites, and norites. The anorthosites are generally inferred to represent floating cumulates in a lunar magma ocean (possible depth 800 km, moon`s radius {approximately}1,738 km). The cumulates that are inferred to be located near the base of the magma ocean are dominantly olivine and pyroxene. The last dregs of the magma ocean are enriched in incompatible elements and have been named KREEP (K, rare earth elements, P). KREEP, formed in this manner, is probably concentrated near the crust/mantle boundary at {approximately}70 km depth. We are attempting to characterize melts parental to ferroan anorthosites and Mg-suite norites by analyzing REEs (La, Ce, Nd, Sm, Eu, Dy, Er, Yb) and Ba, Sr, and Y in their cumulus plagioclase. If the cumulus grains have not been compromised by postcrystallization effects and if we know the relevant mineral/melt partition coefficients (Ds) we can invert the trace element data for plagioclase to parental melt compositions. Melts parental to ferroan anorthosites are estimated to contain REE at concentrations ten to fifty times chondrites. Melts parental to the earlier crystallizing anorthosites (lower REE) have virtually no Eu anomaly, while melts parental to later crystallizing anorthosites (higher REE) have small negative Eu anomalies. This is qualitatively consistent with the fractionation of Eu relative to other REE by crystallization of plagioclase with large positive Eu anomalies. Melts parental to the Mg-suite have much higher total REE and very large negative Eu anomalies. 42 refs., 5 figs., 4 tabs.

  8. Ion microprobe magnesium isotope analysis of plagioclase and hibonite from ordinary chondrites

    NASA Technical Reports Server (NTRS)

    Hinton, R. W.; Bischoff, A.

    1984-01-01

    Ion and electron microprobes were used to examine Mg-26 excesses from Al-26 decay in four Al-rich objects from the type 3 ordinary hibonite clast in the Dhajala chondrite. The initial Al-26/Al-27 ratio was actually significantly lower than Al-rich inclusions in carbonaceous chondrites. Also, no Mg-26 excesses were found in three plagioclase-bearing chondrules that were also examined. The Mg-26 excesses in the hibonite chondrites indicated a common origin for chondrites with the excesses. The implied Al-26 content in a proposed parent body could not, however, be confirmed as a widespread heat source in the early solar system.

  9. Change in Magma Dynamics at Okataina Rhyolite Caldera revealed by Plagioclase Textures and Geochemistry

    NASA Astrophysics Data System (ADS)

    Shane, P. A. R.

    2015-12-01

    A fundamental reorganization of magma dynamics at Okataina volcano, New Zealand, occurred at 26 ka involving a change from smaller volume, high-temperature rhyodacite magmas to a lower eruptive tempo of larger volume, low-temperature, rhyolite magmas. Zircon studies demonstrate the presence of a periodically active, long-lived (100,000 yr) magmatic reservoir. However, there is little correlation between periods of zircon crystallization and eruption events. In contrast, the changing magmatic dynamics is revealed in plagioclase growth histories. Crystals from the ~0.7 ka Kaharoa eruption are characterized by resorbed cores displaying a cellular-texture of high-An (>40) zones partially replaced by low-An (<30) zones, surrounded by a resorption surface and a prominent normal-zoned rim (An50-20). Elevated An, Fe, Mg, Sr and Ti follow the resorption surface and display rimward depletion trends, accompanied by Ba and REE enrichment. The zonation is consistent with fractional crystallization and cooling. The cores display wide trace element diversity, pointing to crystallization in a variety of melts, before transport and mixing into a common magma where the rims grew. Plagioclase from the ~36 ka Hauparu eruption display several regrowth zones separated by resorption surfaces, which surround small resorbed cores with a spongy cellular texture of variable An content (An 40-50). The crystals display step-wise re-growth of successively higher An, Fe, Mg and Ti content, consistent with progressive mafic recharge. Two crystal groups are distinguished by trace element chemistry indicating growth in separate melts and co-occurrence via magma-mingling. The contrasting zoning patterns in plagioclase correspond to the evolutionary history of magmatism at Okataina. Emptying of the magma reservoir following caldera eruption at 46 ka reduced barriers to mafic magma ascent. This is recorded by the frequent resorption and recharge episodes in Hauparu crystals. Subsequent re

  10. Diffuse reflectance spectra of orthopyroxene, olivine, and plagioclase as a function of composition and structure

    NASA Technical Reports Server (NTRS)

    Zolensky, M. E.; Le, L.; Galindo, C.; Morris, R.; Lauer, V.; Vilas, F.

    1993-01-01

    Although many similarities exist between meteorite spectra and 'primitive' asteroids, there are unexplained discrepancies. These discrepancies do not appear to arise from grain size effects. Assuming that primitive meteorites did in fact originate from the 'primitive' asteroids, we believe that there are two testable explanations for the observed spectral discrepancies: compositional or structural differences. We have begun to synthesize and collect reflectance and Mossbauer spectra of pertinent materials, beginning with olivine, pyroxene, and plagioclase (all found in primitive meteorites), and to assess the possible effects composition may have on spectral features. Our study focuses on the combination of composition and structural effects.

  11. Electrolytic method to make alkali alcoholates using ion conducting alkali electrolyte/separator

    SciTech Connect

    Joshi, Ashok V.; Balagopal, Shekar; Pendelton, Justin

    2011-12-13

    Alkali alcoholates, also called alkali alkoxides, are produced from alkali metal salt solutions and alcohol using a three-compartment electrolytic cell. The electrolytic cell includes an anolyte compartment configured with an anode, a buffer compartment, and a catholyte compartment configured with a cathode. An alkali ion conducting solid electrolyte configured to selectively transport alkali ions is positioned between the anolyte compartment and the buffer compartment. An alkali ion permeable separator is positioned between the buffer compartment and the catholyte compartment. The catholyte solution may include an alkali alcoholate and alcohol. The anolyte solution may include at least one alkali salt. The buffer compartment solution may include a soluble alkali salt and an alkali alcoholate in alcohol.

  12. Process for recovering alkali metals and sulfur from alkali metal sulfides and polysulfides

    DOEpatents

    Gordon, John Howard; Alvare, Javier

    2016-10-25

    Alkali metals and sulfur may be recovered from alkali monosulfide and polysulfides in an electrolytic process that utilizes an electrolytic cell having an alkali ion conductive membrane. An anolyte solution includes an alkali monosulfide, an alkali polysulfide, or a mixture thereof and a solvent that dissolves elemental sulfur. A catholyte includes molten alkali metal. Applying an electric current oxidizes sulfide and polysulfide in the anolyte compartment, causes alkali metal ions to pass through the alkali ion conductive membrane to the catholyte compartment, and reduces the alkali metal ions in the catholyte compartment. Liquid sulfur separates from the anolyte solution and may be recovered. The electrolytic cell is operated at a temperature where the formed alkali metal and sulfur are molten.

  13. Alkali and transition metal phospholides

    NASA Astrophysics Data System (ADS)

    Bezkishko, I. A.; Zagidullin, A. A.; Milyukov, V. A.; Sinyashin, O. G.

    2014-06-01

    Major tendencies in modern chemistry of alkali and transition metal phospholides (phosphacyclopentadienides) are systematized, analyzed and generalized. Basic methods of synthesis of these compounds are presented. Their chemical properties are considered with a special focus on their complexing ability. Potential applications of phospholides and their derivatives are discussed. The bibliography includes 184 references.

  14. Raman Spectroscopic Characterization of the Feldspars: Implications for Surface Mineral Characterization in Planetary Exploration

    NASA Technical Reports Server (NTRS)

    Freeman, J. J.; Wang, Alian; Kuebler, K. E.; Haskin, L. A.

    2003-01-01

    The availability in the last decade of improved Raman instrumentation using small, stable, intense lasers, sensitive CCD array detectors, and advanced fast grating systems enabled us to develop the Mars Microbeam Raman Spectrometer (MMRS), a field-portable Raman spectrometer with precision and accuracy capable of identifying minerals and their different compositions. For example, we can determine Mg cation ratios in pyroxenes and olivines to +/-0.1 on the basis of Raman peak positions. Feldspar is another major mineral formed in igneous systems whose characterization is important for determining rock petrogenesis and alteration. From their Raman spectral pattern, feldspars can be readily distinguished from ortho- and chain-silicates and from other tecto-silicates such as quartz and zeolites. We show here how well Raman spectral analysis can distinguish among members within the feldspar group.

  15. A Clinopyroxene-Plagioclase Geobarometer for A-type Silicic Volcanic Rocks

    NASA Astrophysics Data System (ADS)

    Wolff, J.; Iveson, A. A.; Davis, K.; Johnson, T. A.; Gahagan, S.; Ellis, B. S.

    2015-12-01

    Constraining the crustal storage depths of magmas is important in understanding volcanism. The reaction: anorthite (pl) = Ca-Tschermak's (cpx) + silica (Q or liq) has a large volume change and hence offers potential as a geobarometer, but has not been extensively exploited as such. One of the chief barriers to its wide application is consistent estimation of melt silica activity for assemblages that lack quartz. We have skirted this problem by confining attention to metaluminous silicic compositions (SiO2 > 60% by weight), for which silica activity during crystallization is presumed to be close to 1, and calibrated the barometer for the range 0 - 2 GPa using the LEPR database and additional experiments from the literature. Additional improvement is obtained by excluding hydrous phase-bearing assemblages. Despite the analytical uncertainties present in older experimental investigations, with knowledge of temperature, and clinopyroxene, plagioclase and host melt compositions, pressures for amphibole- and biotite-free dacites and rhyolites can be estimated to ±0.17 GPa (1 sigma). The limitations of the barometer render it most applicable to intraplate, A-type rhyolites. Application to one such system, the Snake River Plain rhyolites, indicate that both melt-hosted phenocrysts and clinopyroxene-plagioclase aggregate grains found in these rhyolites formed at low pressures, <0.5 GPa. This is consistent with isotopic evidence for a shallow crustal origin for Snake River Plain rhyolites.

  16. Trace element partitioning between high-An plagioclase and basaltic to basaltic andesite melt at 1 atmosphere pressure

    NASA Astrophysics Data System (ADS)

    Tepley, Frank J., III; Lundstrom, Craig C.; McDonough, William F.; Thompson, Amy

    2010-07-01

    We determined plagioclase-melt partition coefficients for 18 elements by performing controlled cooling rate, 1-atmosphere experiments using both natural and synthetic basaltic (51 wt.% SiO 2) and basaltic andesite (56 wt.% SiO 2) powders in a vertical quench furnace. The experiments produced An 69 to An 87 composition plagioclase. Three starting powders were Gorda Ridge basalt, synthetic diopside (40%)-albite (28%)-anorthite (32%) mixture, and Arenal volcano (Costa Rica) basaltic andesite. The Gorda and synthetic powders were doped at both low concentrations (20-200 ppm) and high concentration (200-5000 ppm), whereas the Arenal powder was doped only at high concentrations resulting in two doped Gorda powders (low: NP, and high: SDP), two doped diopside/albite/anorthite powders (low: DAD, high: SDD) and one doped Arenal powder (high: AR99-2). Trace elements concentrations in both glass and plagioclase were measured by secondary ion mass spectrometry (SIMS) and/or by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). Results for the partitioning of trace elements between plagioclase and melt at different doping levels demonstrate both adherence to Henry's Law and good agreement between the different analytical techniques. In general, plagioclase-melt partition coefficients determined in the An 69-73 range are similar to other published values, however, some of those occurring for plagioclase compositions > An 75 are distinctly lower than those predicted by current regression formulations. We applied a two-lattice melt model to these data to account for differences in melt composition and temperature and found that there were no aberrations associated with partition coefficients. A new set of regression formulations is determined involving the newly determined dataset for plagioclase with An contents between 75 and 87.

  17. 40Ar/39Ar dating of Quaternary feldspar: examples from the Taupo Volcanic Zone, New Zealand

    USGS Publications Warehouse

    Pringle, M.S.; McWilliams, M.; Houghton, B.F.; Lanphere, M.A.; Wilson, C.J.N.

    1992-01-01

    Using a continuous laser and resistance furnace, we have measured ages on Quaternary plagioclase with an absolute precision of about ??30 ka and on Quaternary sanidine with a relative precision of better than 1%. Such precision was achieved by using low-temperature heating steps to remove much of the nonradiogenic argon contamination. Plagioclase is one of the most common mineral phases in volcanic rocks; thus, these procedures will be widely applicable to many problems for which precise radiometric age control has not been available. We studied plagioclase and plagioclase-sanidine concentrates from the oldest and the three largest silicic ash-flow deposits of the Taupo Volcanic Zone, New Zealand, one of the world's largest and most active volcanic systems. The results are in close agreement with new magnetostratigraphic data, suggesting that existing fission-track age determinations significantly underestimate the age of older units, and shift the inception of Taupo Vaolcanic Zone volcanism back to at least 1600 ka. -from Authors

  18. Chromite-plagioclase assemblages as a new shock indicator; implications for the shock and thermal histories of ordinary chondrites

    NASA Astrophysics Data System (ADS)

    Rubin, Alan E.

    2003-07-01

    Chromite in ordinary chondrites (OC) can be used as a shock indicator. A survey of 76 equilibrated H, L and LL chondrites shows that unshocked chromite grains occur in equant, subhedral and rounded morphologies surrounded by silicate or intergrown with metallic Fe-Ni and/or troilite. Some unmelted chromite grains are fractured or crushed during whole-rock brecciation. Others are transected by opaque veins; the veins form when impacts cause localized heating of metal-troilite intergrowths above the Fe-FeS eutectic (988°C), mobilization of metal-troilite melts, and penetration of the melt into fractures in chromite grains. Chromite-plagioclase assemblages occur in nearly every shock-stage S3-S6 OC; the assemblages range in size from 20-300 μm and consist of 0.2-20-μm-size euhedral, subhedral, anhedral and rounded chromite grains surrounded by plagioclase or glass of plagioclase composition. Plagioclase has a low impedance to shock compression. Heat from shock-melted plagioclase caused adjacent chromite grains to melt; chromite grains crystallized from this melt. Those chromite grains in the assemblages that are completely surrounded by plagioclase are generally richer in Al 2O 3 than unmelted, matrix chromite grains in the same meteorite. Chromite veinlets (typically 0.5-2 μm thick and 10-300 μm long) occur typically in the vicinity of chromite-plagioclase assemblages. The veinlets formed from chromite-plagioclase melts that were injected into fractures in neighboring silicate grains; chromite crystallized in the fractures and the residual plagioclase-rich melt continued to flow, eventually pooling to form plagioclase-rich melt pockets. Chromite-rich "chondrules" (consisting mainly of olivine, plagioclase-normative mesostasis, and 5-15 vol.% chromite) occur in many shocked OC and OC regolith breccias but they are absent from primitive type-3 OC. They may have formed by impact melting chromite, plagioclase and adjacent mafic silicates during higher-energy shock

  19. Chromite-Plagioclase Assemblages as a New Shock Indicator; Implications for the Shock and Thermal Histories of Ordinary Chondrites

    NASA Technical Reports Server (NTRS)

    Rubin, Alan E.

    2006-01-01

    Chromite in ordinary chondrites (OC) can be used as a shock indicator. A survey of 76 equilibrated H, L and LL chondrites shows that unshocked chromite grains occur in equant, subhedral and rounded morphologies surrounded by silicate or intergrown with metallic Fe-Ni and/or troilite. Some unmelted chromite grains are fractured or crushed during whole-rock brecciation. Others are transected by opaque veins; the veins form when impacts cause localized heating of metal-troilite intergrowths above the Fe-FeS eutectic (988 C), mobilization of metal-troilite melts, and penetration of the melt into fractures in chromite grains. Chromite-plagioclase assemblages occur in nearly every shock-stage S3-S6 OC; the assemblages range in size from 20-300 microns and consist of 0.2-20-micron-size euhedral, subhedral, anhedral and rounded chromite grains surrounded by plagioclase or glass of plagioclase composition. Plagioclase has a low impedance to shock compression. Heat from shock-melted plagioclase caused adjacent chromite grains to melt; chromite grains crystallized from this melt. Those chromite grains in the assemblages that are completely surrounded by plagioclase are generally richer in Al2O3, than unmelted, matrix chromite grains in the same meteorite. Chromite veinlets (typically 0.5-2 microns thick and 10-300 microns long) occur typically in the vicinity of chromite-plagioclase assemblages. The veinlets formed from chromite-plagioclase melts that were injected into fractures in neighboring silicate grains; chromite crystallized in the fractures and the residual plagioclase-rich melt continued to flow, eventually pooling to form plagioclase-rich melt pockets. Chromite-rich chondrules (consisting mainly of olivine, plagioclase-normative mesostasis, and 5-15 vol.% chromite) occur in many shocked OC and OC regolith breccias but they are absent from primitive type-3 OC. They may have formed by impact melting chromite, plagioclase and adjacent mafic silicates during higher

  20. The importance of feldspar for ice nucleation by mineral dust in mixed-phase clouds.

    PubMed

    Atkinson, James D; Murray, Benjamin J; Woodhouse, Matthew T; Whale, Thomas F; Baustian, Kelly J; Carslaw, Kenneth S; Dobbie, Steven; O'Sullivan, Daniel; Malkin, Tamsin L

    2013-06-20

    The amount of ice present in mixed-phase clouds, which contain both supercooled liquid water droplets and ice particles, affects cloud extent, lifetime, particle size and radiative properties. The freezing of cloud droplets can be catalysed by the presence of aerosol particles known as ice nuclei. One of the most important ice nuclei is thought to be mineral dust aerosol from arid regions. It is generally assumed that clay minerals, which contribute approximately two-thirds of the dust mass, dominate ice nucleation by mineral dust, and many experimental studies have therefore focused on these materials. Here we use an established droplet-freezing technique to show that feldspar minerals dominate ice nucleation by mineral dusts under mixed-phase cloud conditions, despite feldspar being a minor component of dust emitted from arid regions. We also find that clay minerals are relatively unimportant ice nuclei. Our results from a global aerosol model study suggest that feldspar ice nuclei are globally distributed and that feldspar particles may account for a large proportion of the ice nuclei in Earth's atmosphere that contribute to freezing at temperatures below about -15 °C.

  1. I-Xe Record of Cooling in K-Feldspar Inclusion from the Colomera (IIE) Iron

    NASA Technical Reports Server (NTRS)

    Pravdivtseva, Olga; Meshik, Alex; Hohenberg, Charles M.; Wasserburg, Gerald J.

    2000-01-01

    Individual mineral grains from a silicate inclusion of the Colomera IIE iron meteorite were studied by laser extraction to find suitable host phases for I-Xe dating. K-feldspar separate yields an I-Xe age of 4.552 Ga and a cooling rate of 4-16 C/Ma.

  2. Preferential cataclastic grain size reduction of feldspar in deformation bands in poorly consolidated arkosic sands

    PubMed Central

    Exner, Ulrike; Tschegg, Cornelius

    2012-01-01

    This study presents microstructural as well as bulk and mineral chemical investigations of deformation bands in uncemented, friable arkosic sands of Miocene age (Vienna Basin, Austria). Our microstructural study indicates grain size reduction by grain flaking in deformation bands with small offsets (0.5–8 cm), and dominant intragranular fracturing and cataclasis of altered feldspar grains at larger displacements (up to 60 cm). Relative to quartz, the sericitized feldspar grains are preferably fractured and abraded, which additionally leads to an enrichment of mainly phyllosilicates by mechanical expulsion from feldspar. Both cataclasis of quartz and feldspar grains and enrichment of phyllosilicates result in grain size reduction within the deformation bands. The measured reduction in porosity of up to 20% is in some cases associated with a permeability reduction, reflected in the retention of iron-oxide rich fluids along deformation bands. These deformation bands formed at very shallow burial depths in unconsolidated sediments indicate that fault sealing may occur in the absence of chemical alteration of the deformation bands and lead to a compartmentalization of a groundwater or hydrocarbon reservoir. PMID:26523078

  3. Preferential cataclastic grain size reduction of feldspar in deformation bands in poorly consolidated arkosic sands

    NASA Astrophysics Data System (ADS)

    Exner, Ulrike; Tschegg, Cornelius

    2012-10-01

    This study presents microstructural as well as bulk and mineral chemical investigations of deformation bands in uncemented, friable arkosic sands of Miocene age (Vienna Basin, Austria). Our microstructural study indicates grain size reduction by grain flaking in deformation bands with small offsets (0.5-8 cm), and dominant intragranular fracturing and cataclasis of altered feldspar grains at larger displacements (up to 60 cm). Relative to quartz, the sericitized feldspar grains are preferably fractured and abraded, which additionally leads to an enrichment of mainly phyllosilicates by mechanical expulsion from feldspar. Both cataclasis of quartz and feldspar grains and enrichment of phyllosilicates result in grain size reduction within the deformation bands. The measured reduction in porosity of up to 20% is in some cases associated with a permeability reduction, reflected in the retention of iron-oxide rich fluids along deformation bands. These deformation bands formed at very shallow burial depths in unconsolidated sediments indicate that fault sealing may occur in the absence of chemical alteration of the deformation bands and lead to a compartmentalization of a groundwater or hydrocarbon reservoir.

  4. Re-Examination of Anomalous I-Xe Ages: Orgueil and Murchison Magnetites and Allegan Feldspar

    NASA Technical Reports Server (NTRS)

    Hohenberg, Charles M.; Pravdivtseva, Olga V.; Meshik, Alex P.

    2000-01-01

    Old I-Xe age for Orgueil (and Murchison) magnetite is not confirmed. New results show closure 2.8 Ma after Shallowater/Bjurbole standard, 10.3 Ma later than previously reported. The anomalously old I-Xe age of Allegan feldspar is attributed to shock.

  5. SCR neon and argon in Kapoeta feldspar: Evidence for an active ancient Sun

    NASA Technical Reports Server (NTRS)

    Rao, M. N.; Garrison, D. H.; Bogard, D. D.

    1993-01-01

    From etched feldspar size-fractions of Kapoeta, we determine a significant excess of cosmogenic Ne-21 and Ar-38 over that produced by galactic cosmic rays. This excess component is attributed to early production by energetic solar protons and suggest that the energetic proton flux from the ancient Sun was several hundred times more intense than that of the contemporary Sun.

  6. Alkali metal/sulfur battery

    DOEpatents

    Anand, Joginder N.

    1978-01-01

    Alkali metal/sulfur batteries in which the electrolyte-separator is a relatively fragile membrane are improved by providing means for separating the molten sulfur/sulfide catholyte from contact with the membrane prior to cooling the cell to temperatures at which the catholyte will solidify. If the catholyte is permitted to solidify while in contact with the membrane, the latter may be damaged. The improvement permits such batteries to be prefilled with catholyte and shipped, at ordinary temperatures.

  7. Cryptic young zircon and young plagioclase in the Kaharoa Rhyolite, Tarawera, New Zealand: Implications for crystal recycling in magmatic systems

    NASA Astrophysics Data System (ADS)

    Klemetti, E. W.; Cooper, K. M.

    2007-12-01

    We measured in-situ 238U-230Th zircon and bulk plagioclase 238U-230Th-226Ra disequilibria in rhyolite lava and tephra from the ~1315 AD Kaharoa eruption of Tarawera Volcano, New Zealand in order to constrain its history of chemical evolution. These data suggest that zircon records a protracted history (10s of kyr) whereas plagioclase is dominantly young (few kyr), but both phases crystallize up to the eruption. The Kaharoa eruptive period at Tarawera consists of ~2.5 km3 of crystal-rich rhyolite (74-75 wt% silica) lava and ~5 km3 of coeval tephra deposits, making it the largest silicic eruption in New Zealand in the last 1,000 years. 238U-230Th disequilibria measurements of zircon determined via SHRIMP-RG analyses produce an array of ages, with three main populations: (1) within error of eruption age; (2) 15-80 k.y.; (3) 100-175 k.y. Very few analyzed zircon fall within error of eruption age and little difference is seen in the age distribution of zircon between the lava and tephra. In contrast, 238U-230Th and 230Th-226Ra plagioclase ages appear to be within error of eruption age however this age is complicated zircon inclusions in the plagioclase. This contamination by zircon is seen in the 238U-230Th disequilibria and trace element data, where the addition of zircon pushes the bulk plagioclase separate towards more U-enriched values and high Zr values. However, the (230Th)/(232Th) ratios for the separates are the same as the whole rock values, indicating that any zircon in the bulk separate must be young (eruption age). This finding is also borne out in 230Th-226Ra disequilibria, where zero-age zircon contamination is reflected in increased (230Th)/[Ba] with no change in (226Ra)/[Ba]. In both cases, as little as 1 ppm of zero-age zircon contamination is needed to create these patterns. This signal of young plagioclase and zircon growth is in contrast to the protracted history seen in the SHRIMP-RG zircon data. This suggests that young zircon growth in the Kaharoa

  8. High geomagnetic intensity during the mid-Cretaceous from Thellier analyses of single plagioclase crystals.

    PubMed

    Tarduno, J A; Cottrell, R D; Smirnov, A V

    2001-03-01

    Recent numerical simulations have yielded the most efficient geodynamo, having the largest dipole intensity when reversal frequency is low. Reliable paleointensity data are limited but heretofore have suggested that reversal frequency and paleointensity are decoupled. We report data from 56 Thellier-Thellier experiments on plagioclase crystals separated from basalts of the Rajmahal Traps (113 to 116 million years old) of India that formed during the Cretaceous Normal Polarity Superchron. These data suggest a time-averaged paleomagnetic dipole moment of 12.5 +/- 1.4 x 10(22) amperes per square meter, three times greater than mean Cenozoic and Early Cretaceous-Late Jurassic dipole moments when geomagnetic reversals were frequent. This result supports a correlation between intervals of low reversal frequency and high geomagnetic field strength. PMID:11230692

  9. [Energy related studies utilizing K-feldspar thermochronology]. Progress report, 1991--1992

    SciTech Connect

    Not Available

    1992-03-01

    In our second year of current funding cycle, we have investigated the Ar diffusion properties and microstructures of K-feldspars and the application of domain theory to natural K-feldspars. We completed a combined TEM and argon diffusion study of the effect of laboratory heat treatment on the microstructure and kinetic properties of K-feldspar. We conclude in companion papers that, with one minor exception, no observable change in the diffusion behavior occurs during laboratory extraction procedures until significant fusion occurs at about 1100{degrees}C. The effect that is observed involves a correlation between the homogenization of cryptoperthite lamelle and the apparent increase in retentivity of about 5% of the argon in the K-feldspar under study. We can explain this effect of both as an artifact of the experiment or the loss of a diffusion boundary. Experiments are being considered to resolve this question. Refinements have been made to our experimental protocol that appears that greatly enhance the retrieval of multi-activation energies from K-feldspars. We have applied the multi-domain model to a variety of natural environments (Valles Caldera, Red River fault, Appalachian basin) with some surprising results. Detailed {sup 40}Ar/{sup 39} Ar coverage of the Red River shear zone, thought to be responsible for the accommodation of a significant fraction of the Indo-Asian convergence, strongly suggests that our technique can precisely date both the termination of ductile strike-slip motion and the initiation of normal faulting. Work has continued on improving our numerical codes for calculating thermal histories and the development of computer based graphing tools has significantly increased our productivity.

  10. Strong climate and tectonic control on plagioclase weathering in granitic terrain

    USGS Publications Warehouse

    Rasmussen, C.; Brantley, S.; Richter, D.D.B.; Blum, A.; Dixon, J.; White, A.F.

    2011-01-01

    Investigations to understand linkages among climate, erosion and weathering are central to quantifying landscape evolution. We approach these linkages through synthesis of regolith data for granitic terrain compiled with respect to climate, geochemistry, and denudation rates for low sloping upland profiles. Focusing on Na as a proxy for plagioclase weathering, we quantified regolith Na depletion, Na mass loss, and the relative partitioning of denudation to physical and chemical contributions. The depth and magnitude of regolith Na depletion increased continuously with increasing water availability, except for locations with mean annual temperature <5??C that exhibited little Na depletion, and locations with physical erosion rates <20gm-2yr-1 that exhibited deep and complete regolith Na depletion. Surface Na depletion also tended to decrease with increasing physical erosion. Depth-integrated Na mass loss and regolith depth were both three orders of magnitude greater in the fully depleted, low erosion rate sites relative to other locations. These locations exhibited strong erosion-limitation of Na chemical weathering rates based on correlation of Na chemical weathering rate to total Na denudation. Sodium weathering rates in cool locations with positive annual water balance were strongly correlated to total Na denudation and precipitation, and exhibited an average apparent activation energy (Ea) of 69kJmol-1 Na. The remaining water-limited locations exhibited kinetic limitation of Na weathering rates with an Ea of 136kJmol-1 Na, roughly equivalent to the sum of laboratory measures of Ea and dissolution reaction enthalpy for albite. Water availability is suggested as the dominant factor limiting rate kinetics in the water-limited systems. Together, these data demonstrate marked transitions and nonlinearity in how climate and tectonics correlate to plagioclase chemical weathering and Na mass loss. ?? 2010 Elsevier B.V.

  11. Sims Analysis of Water Abundance and Hydrogen Isotope in Lunar Highland Plagioclase

    NASA Technical Reports Server (NTRS)

    Hui, Hejiu; Guan, Yunbin; Chen, Yang; Peslier, Anne H.; Zhang, Youxue; Liu, Yang; Rossman, George R.; Eiler, John M.; Neal, Clive R.

    2015-01-01

    The detection of indigenous water in mare basaltic glass beads has challenged the view established since the Apollo era of a "dry" Moon. Since this discovery, measurements of water in lunar apatite, olivine-hosted melt inclusions, agglutinates, and nominally anhydrous minerals have confirmed that lunar igneous materials contain water, implying that some parts of lunar mantle may have as much water as Earth's upper mantle. The interpretation of hydrogen (H) isotopes in lunar samples, however, is controversial. The large variation of H isotope ratios in lunar apatite (delta Deuterium = -202 to +1010 per mille) has been taken as evidence that water in the lunar interior comes from the lunar mantle, solar wind protons, and/or comets. The very low deuterium/H ratios in lunar agglutinates indicate that solar wind protons have contributed to their hydrogen content. Conversely, H isotopes in lunar volcanic glass beads and olivine-hosted melt inclusions being similar to those of common terrestrial igneous rocks, suggest a common origin for water in both Earth and Moon. Lunar water could be inherited from carbonaceous chondrites, consistent with the model of late accretion of chondrite-type materials to the Moon as proposed by. One complication about the sources of lunar water, is that geologic processes (e.g., late accretion and magmatic degassing) may have modified the H isotope signatures of lunar materials. Recent FTIR analyses have shown that plagioclases in lunar ferroan anorthosite contain approximately 6 ppm H2O. So far, ferroan anorthosite is the only available lithology that is believed to be a primary product of the lunar magma ocean (LMO). A possible consequence is that the LMO could have contained up to approximately 320 ppm H2O. Here we examine the possible sources of water in the LMO through measurements of water abundances and H isotopes in plagioclase of two ferroan anorthosites and one troctolite from lunar highlands.

  12. Dislocation generation, slip systems, and dynamic recrystallization in experimentally deformed plagioclase single crystals

    NASA Astrophysics Data System (ADS)

    Stünitz, H.; Fitz Gerald, J. D.; Tullis, J.

    2003-09-01

    Three samples of gem quality plagioclase crystals of An60 were experimentally deformed at 900 °C, 1 GPa confining pressure and strain rates of 7.5-8.7×10 -7 s -1. The starting material is effectively dislocation-free so that all observed defects were introduced during the experiments. Two samples were shortened normal to one of the principal slip planes (010), corresponding to a "hard" orientation, and one sample was deformed with a Schmid factor of 0.45 for the principal slip system [001](010), corresponding to a "soft" orientation. Several slip systems were activated in the "soft" sample: dislocations of the [001](010) and <110>(001) system are about equally abundant, whereas <110>{111} and [101] in (1¯31) to (2¯42) are less common. In the "soft" sample plastic deformation is pervasive and deformation bands are abundant. In the "hard" samples the plastic deformation is concentrated in rims along the sample boundaries. Deformation bands and shear fractures are common. Twinning occurs in close association with fracturing, and the processes are clearly interrelated. Glissile dislocations of all observed slip systems are associated with fractures and deformation bands indicating that deformation bands and fractures are important sites of dislocation generation. Grain boundaries of tiny, defect-free grains in healed fracture zones have migrated subsequent to fracturing. These grains represent former fragments of the fracture process and may act as nuclei for new grains during dynamic recrystallization. Nucleation via small fragments can explain a non-host-controlled orientation of recrystallized grains in plagioclase and possibly in other silicate materials which have been plastically deformed near the semi-brittle to plastic transition.

  13. Oxalate adsorption at a plagioclase (An47) surface and models for ligand-promoted dissolution

    USGS Publications Warehouse

    Stillings, L.L.; Drever, J.I.; Poulson, S.R.

    1998-01-01

    Previous work on adsorption of oxalate at aluminosilicate surfaces suggests that maximum adsorption occurs through a bidentate attachment of the organic ligand, at near-neutral pH. Rates of ligand-promoted dissolution are expected to be greatest at this pH as well. We tested this model by measuring oxalate adsorption on the surface of andesine (An47), in solutions of pH 3- 5 and total oxalate concentrations of 0-8 mM. Contrary to expectation, the greatest adsorption density of 24 ??mol m-2 total oxalate was observed at pH 3 and 8 mM total oxalate. Adsorption is dependent upon the activities of both oxalate (C2O42-) and bioxalate (HC2O4-) in solution and can be modeled with either a two-term Langmuir or a two-term Freundlich isotherm. A Freundlich adsorption model provided the best fit to rate data because it was not constrained to a finite number of adsorption sites, as was the Langmuir model. The two-term ligand adsorption model was incorporated into a rate model: R(tot) = k(H-)[H(ads)/+](L) + k(HOx-)[HOx(ads)/-] + k(Ox2- )[Ox2(ads)/-] where R(tot) is the net dissolution rate of the feldspar, [i(ads)] is the concentration of species i adsorbed to the surface, and k(i) is the rate constant for release of the surface complex. The model was fit to data for oxalate-promoted dissolution of andesine, resulting in estimates for the rate constants of k(HOx-) = 1.16 x 10-12, k(Ox2-) = 1.05 x 10-12, and k(H-) = 9.61 x 10-13 mol of feldspar (??mol of i) (??mol of i)-1 s-1.Previous work on adsorption of oxalate at aluminosilicate surfaces suggests that maximum adsorption occurs through a bidentate attachment of the organic ligand, at near-neutral pH. Rates of ligand-promoted dissolution are expected to be greatest at this pH as well. We tested this model by measuring oxalate adsorption on the surface of andesine (An47), in solutions of pH 3-5 and total oxalate concentrations of 0-8 mM. Contrary to expectation, the greatest adsorption density of 24 ??mol m-2 total oxalate was

  14. Chemiluminescence from excited c 2- -alkali cation complexes formed in alkali atom-halocarbon flames

    NASA Astrophysics Data System (ADS)

    Lin, K. K.; Balling, L. C.; Wright, J. J.

    1987-01-01

    Vapor phase reactions between alkali atoms and several halocarbon molecules containing C-C bonds have been observed to produce chemiluminescence which appears to originate from C 2-- (alkali) + complexes.

  15. Authigenic K-feldspar in salt rock (Haselgebirge Formation, Eastern Alps)

    NASA Astrophysics Data System (ADS)

    Leitner, Christoph

    2015-04-01

    The crystallisation of authigenic quartz under low temperature, saline conditions is well known (Grimm, 1962). Also the growth of low temperature authigenic feldspar in sediments is a long known phenomenon (Kastner & Siever, 1979; Sandler et al., 2004). In this study we intend to show that halite (NaCl) is a major catalyser for authigenic mineral growth. During late Permian (c. 255-250 Ma), when the later Eastern Alps were located around north of the equator, the evaporites of the Haselgebirge Formation were deposited (Piller et al., 2004). The Haselgebirge Fm. consists in salt mines of a two-component tectonite of c. 50 % halite and 50 % sedimentary clastic and other evaporite rocks (Spötl 1998). Most of the clastic rocks are mud- to siltstones ("mudrock"). During this study, we investigated rare sandstones embedded in salt rock form four Alpine salt mines. Around 40 polished thin sections were prepared by dry grinding for thin section analysis and scanning electron microscopy. The sandstones consist mainly of quartz, K-feldspar, rock fragments, micas, accessory minerals and halite in the pore space. They are fine grained and well sorted. Mudrock clasts in sandstone were observed locally, and also coal was observed repeatedly. Asymmetric ripples were found only in the dimension of millimeters to centimeters. Euhedral halite crystals in pores indicate an early presence of halite. During early diagenesis, authigenic minerals crystallized in the following chronological order. (1) Where carbonate (mainly magnesite) occurred, it first filled the pore space. Plant remains were impregnated with carbonate. (2) Halite precipitated between the detritic sandstone grains. Carbonate grains can be completely embedded in halite. (3) K-feldspar and quartz grains usually expose a detritic core and a later grown euhedral inclusion free rim. Euhedral rims of K-feldspar often also enclose a halite core. K-feldspar replaced the pre-existing halite along former grain boundaries of

  16. Regenerable activated bauxite adsorbent alkali monitor probe

    DOEpatents

    Lee, Sheldon H. D.

    1992-01-01

    A regenerable activated bauxite adsorber alkali monitor probe for field applications to provide reliable measurement of alkali-vapor concentration in combustion gas with special emphasis on pressurized fluidized-bed combustion (PFBC) off-gas. More particularly, the invention relates to the development of a easily regenerable bauxite adsorbent for use in a method to accurately determine the alkali-vapor content of PFBC exhaust gases.

  17. Regenerable activated bauxite adsorbent alkali monitor probe

    DOEpatents

    Lee, S.H.D.

    1992-12-22

    A regenerable activated bauxite adsorber alkali monitor probe for field applications to provide reliable measurement of alkali-vapor concentration in combustion gas with special emphasis on pressurized fluidized-bed combustion (PFBC) off-gas. More particularly, the invention relates to the development of a easily regenerable bauxite adsorbent for use in a method to accurately determine the alkali-vapor content of PFBC exhaust gases. 6 figs.

  18. Alkali-Metal Spin Maser.

    PubMed

    Chalupczak, W; Josephs-Franks, P

    2015-07-17

    Quantum measurement is a combination of a read-out and a perturbation of the quantum system. We explore the nonlinear spin dynamics generated by a linearly polarized probe beam in a continuous measurement of the collective spin state in a thermal alkali-metal atomic sample. We demonstrate that the probe-beam-driven perturbation leads, in the presence of indirect pumping, to complete polarization of the sample and macroscopic coherent spin oscillations. As a consequence of the former we report observation of spectral profiles free from collisional broadening. Nonlinear dynamics is studied through exploring its effect on radio frequency as well as spin noise spectra. PMID:26230788

  19. Alkali-Metal Spin Maser

    NASA Astrophysics Data System (ADS)

    Chalupczak, W.; Josephs-Franks, P.

    2015-07-01

    Quantum measurement is a combination of a read-out and a perturbation of the quantum system. We explore the nonlinear spin dynamics generated by a linearly polarized probe beam in a continuous measurement of the collective spin state in a thermal alkali-metal atomic sample. We demonstrate that the probe-beam-driven perturbation leads, in the presence of indirect pumping, to complete polarization of the sample and macroscopic coherent spin oscillations. As a consequence of the former we report observation of spectral profiles free from collisional broadening. Nonlinear dynamics is studied through exploring its effect on radio frequency as well as spin noise spectra.

  20. Partition coefficients for iron between plagioclase and basalt as a function of oxygen fugacity - Implications for Archean and lunar anorthosites

    NASA Technical Reports Server (NTRS)

    Phinney, W. C.

    1992-01-01

    As a prelude to determinations of the content of total iron as FeO(T) in melts in equilibrium with calcic anorthosites, the partition coefficients (Ds) for FeO(T) between calcic plagioclase and basaltic melt were determined, as a function of oxygen fugacity (f(O2)), for a basaltic composition that occurs as matrices for plagioclase megacrysts. Results showed that, at the liquidus conditions, the value of D for FeO(T) between calcic plagioclase and tholeiitic basalt changed little (from 0.030 to 0.044) between the very low f(O2) of the iron-wustite buffer and that of the quartz-fayalite-magnetite (QFM) buffer. At fugacities above QFM, the value for D increased rapidly to 0.14 at the magnetite-hematite buffer and to 0.33 in air. The increase in D results from the fact that, at f(O2) below QFM, nearly all of the Fe is in the Fe(2+) state; above QFM, the Fe(3+)/Fe(2+) ratio in the melt increases rapidly, causing more Fe to enter the plagioclase which accepts Fe(3+) more readily than Fe(2+).

  1. Valid garnet biotite (GB) geothermometry and garnet aluminum silicate plagioclase quartz (GASP) geobarometry in metapelitic rocks

    NASA Astrophysics Data System (ADS)

    Wu, Chun-Ming; Cheng, Ben-He

    2006-06-01

    At present there are many calibrations of both the garnet-biotite (GB) thermometer and the garnet-aluminum silicate-plagioclase-quartz (GASP) barometer that may confuse geologists in choosing a reliable thermometer and/or barometer. To test the accuracy of the GB thermometers we have applied the various GB thermometers to reproduce the experimental data and data from natural metapelitic rocks of various prograde sequences, inverted metamorphic zones and thermal contact aureoles. We have concluded that the four GB thermometers (Perchuk, L.L., Lavrent'eva, I.V., 1983. Experimental investigation of exchange equilibria in the system cordierite-garnet-biotite. In: Saxena, S.K. (ed.) Kinetics and equilibrium in mineral reactions. Springer-Verlag New York, Berlin, Heidelberg. pp. 199-239.; Kleemann, U., Reinhardt, J., 1994. Garnet-biotite thermometry revised: the effect of Al VI and Ti in biotite. European Journal of Mineralogy 6, 925-941.; Holdaway, M.J., 2000. Application of new experimental and garnet Margules data to the garnet-biotite geothermometer. American Mineralogist 85, 881-892., Model 6AV; Kaneko, Y., Miyano, T., 2004. Recalibration of mutually consistent garnet-biotite and garnet-cordierite geothermometers. Lithos 73, 255-269. Model B) are the most valid and reliable of this kind of thermometer. More specifically, we prefer the Holdaway (Holdaway, M.J., 2000. Application of new experimental and garnet Margules data to the garnet-biotite geothermometer. American Mineralogist 85, 881-892.) and the Kleemann and Reinhardt (Kleemann, U., Reinhardt, J., 1994. Garnet-biotite thermometry revised: the effect of Al VI and Ti in biotite. European Journal of Mineralogy 6, 925-941.) calibrations due to their small errors in reproducing the experimental temperatures and good accuracy in successfully discerning the systematic temperature changes of the different sequences. In addition, after applying the GASP barometer to 335 natural metapelitic samples containing one kind

  2. Multiphase inclusions in plagioclase from anorthosites in the Stillwater Complex, Montana: implications for the origin of the anorthosites

    USGS Publications Warehouse

    Loferski, P.J.; Arculus, R.J.

    1993-01-01

    Multiphase inclusions, consisting of clinopyroxene+ilmenite+apatite, occur within cumulus plagioclase grains from anorthosites in the Stillwater Complex, Montana, and in other rocks from the Middle Banded series of the intrusion. The textures and constant modal mineralogy of the inclusions indicate that they were incorporated in the plagioclase as liquid droplets that later crystallized rather than as solid aggregates. Their unusual assemblage, including a distinctive manganiferous ilmenite and the presence of baddeleyite (ZrO2), indicates formation from an unusual liquid. A process involving silicater liquid immiscibility is proposed, whereby small globules of a liquid enriched in Mg, Fe, Ca, Ti, P, REE, Zr and Mn exsolved from the main liquid that gave rise to the anorthosites, became trapped in the plagioclase, and later crystallized to form the inclusions. The immiscibility could have occurred locally within compositional boundaries around crystallizing plagioclase grains or it could have occurred pervasively throughout the liquid. It is proposed that the two immiscible liquids were analogous, n terms of their melt structures, to immiscible liquid pairs reported in the literature both in experiments and in natural basalts. For the previously reported pairs, immiscibility is between a highly polymerized liquid, typically granitic in composition, and a depolymerized liquid, typically ferrobasaltic in composition. In the case of the anorthosites, the depolymerized liquid is represented by the inclusions, and the other liquid was a highly polymerized aluminosilicate melt with a high normative plagioclase content from which the bulk of the anorthosites crystallized. Crystallization of the anorthosites from this highly polymerized liquid accounts for various distinctive textural and chemical features of the anorthosites compared to other rocks in the Stillwater Complex. A lack of correlation between P contents and chondrite-normalized rare earth element (REE) ratios

  3. Application of the Plagioclase-Liquid Hygrometer to the Bishop Tuff: Consistency with Melt Inclusion H2O Contents

    NASA Astrophysics Data System (ADS)

    Jolles, J.; Lange, R. A.

    2015-12-01

    High-silica (74-77 wt% SiO2) rhyolites are the most evolved magmas on Earth and constitute some of the largest eruptions (1000s of km3). Of these, one classic example is the Bishop Tuff, a 760 ka eruption of >670 km3 of high-silica rhyolite erupted from Long Valley caldera, CA. Documenting dissolved H2O contents is crucial for understanding its origin and evolution. Analyses of water contents measured in quartz-hosted melt inclusions from the Bishop Tuff (Wallace et al. 1999; Anderson et al. 2000) show that the Early and Middle Bishop Tuff (Ig1Eb, Ig2Ea) have higher water contents (≤ 6.3 wt% H2O) than the Late Bishop Tuff (Ig2NWa; ≤ 5.2 wt%). Our work utilizes the revised plagioclase-liquid hygrometer (Waters & Lange, 2015), which is applicable to rhyolite, to evaluate internal consistency between Fe-Ti oxide temperatures, the plagioclase hygrometer, and melt inclusion H2O analyses. Two-oxide thermometry (Ghiorso & Evans, 2008), using all possible Fe-Ti oxide pairs (between 56 and 1500 pairs for individual samples), was carried out on 2-3 pumice clasts for each sampled eruptive unit. Resulting temperatures (°C ± 1σ) for individual clasts are: 705 ± 12, 728 ± 10 for unit Ig1Eb; 710 ± 12, 728 ± 11 for unit Ig2Ea; 752 ±10, 776 ± 8, 778 ± 7 for unit Ig2NWa; 791 ± 7, 795 ± 8 for unit Ig2Nb. The compositions of the most calcic plagioclase phenocrysts in the Early and Middle units are An17-19, whereas in the Late units they are An29-30. When the Fe-Ti oxide temperatures, whole rock analyses, and plagioclase compositions are incorporated into the plagioclase hygrometer, they give water contents at the onset of plagioclase crystallization of 6.6-6.9 wt% for the Early and Middle units and 4.8-4.9 wt % for the Late units. These results show internal consistency between melt inclusion analyses of water, Fe-Ti oxide thermometry, and the plagioclase-liquid hygrometer; they further support a temperature gradient across the Early, Middle, and Late Bishop Tuff units.

  4. Diffusion-Reaction Between Basaltic Andesite and Gabbro at 0.5 GPa: an Explanation for Anorthitic Plagioclase?

    NASA Astrophysics Data System (ADS)

    Lundstrom, C. C.; Boudreau, A. E.; Pertermann, M.

    2004-12-01

    Despite the remarkably smooth variation in bulk composition of erupted lavas at Arenal volcano (1968-2003), mineral compositions vary widely. Plagioclase ranges from An52 to An95 while Cr2O3 in CPX varies from 0.7 to 0.05 wt % (Streck et al., 2003). To address the question "how do bulk compositions remain near-steady-state while crystal compositions vary widely," we have performed 2 diffusion-reaction experiments in the piston cylinder at 0.5 GPa. These juxtaposed Arenal basaltic andesite AR-8 at 1200° C with a Stillwater Complex gabbro, lying in a thermal gradient toward the piston. In one experiment, we synthesized a glass-plagioclase (An67-75) aggregate of AR-8 in a graphite-Pt-Ti capsule at P-T, polished one end, dried tracer solutions of 45Ca, 6Li, 84Sr and 136Ba on its surface, and juxtaposed it with gabbro for 13 days. Profiles of bulk composition as a function of distance from the interface show that AR-8 gains Al2O3, MgO and CaO from the gabbro and loses Na2O, K2O, SiO2 and FeO to it. Notably, a plagioclase rich (65%) layer develops at the interface between the two materials as CPX disappears. This layer and the compositional profiles are reproduced by diffusion-reaction models using IRIDIUM (Boudreau, 2003). Plagioclase at the interface develops a texture of homogeneous anorthitic cores (An90) that abruptly shift to 10μ m rims having compositions (An67) in Na-Ca exchange equilibrium with the co-existing melt. A beta track map shows that 45Ca is incorporated into the plagioclase cores while SIMS analyses indicate isotopic equilibration between core and melt. Thus, these anorthitic plagioclase result from diffusion-reaction with efficient chemical communication between the melt and the plagioclase core. Microchannels cutting through the rim, rather than solid-state diffusion, appear to control re-equilibration. Other observations from the experiment parallel Arenal lavas: Mg# variation in OPX is small in both experiments and lavas while profiles of Cr

  5. Microfluidic Leaching of Soil Minerals: Release of K+ from K Feldspar.

    PubMed

    Ciceri, Davide; Allanore, Antoine

    2015-01-01

    The rate of K+ leaching from soil minerals such as K-feldspar is believed to be too slow to provide agronomic benefit. Currently, theories and methods available to interpret kinetics of mineral processes in soil fail to consider its microfluidic nature. In this study, we measure the leaching rate of K+ ions from a K-feldspar-bearing rock (syenite) in a microfluidic environment, and demonstrate that at the spatial and temporal scales experienced by crop roots, K+ is available at a faster rate than that measured with conventional apparatuses. We present a device to investigate kinetics of mineral leaching at an unprecedented simultaneous resolution of space (~101-102 μm), time (~101-102 min) and fluid volume (~100-101 mL). Results obtained from such a device challenge the notion that silicate minerals cannot be used as alternative fertilizers for tropical soils. PMID:26485160

  6. Quantitative analysis of time-resolved infrared stimulated luminescence in feldspars

    NASA Astrophysics Data System (ADS)

    Pagonis, Vasilis; Ankjærgaard, Christina; Jain, Mayank; Chithambo, Makaiko L.

    2016-09-01

    Time-resolved infrared-stimulated luminescence (TR-IRSL) from feldspar samples is of importance in the field of luminescence dating, since it provides information on the luminescence mechanism in these materials. In this paper we present new analytical equations which can be used to analyze TR-IRSL signals, both during and after short infrared stimulation pulses. The equations are developed using a recently proposed kinetic model, which describes localized electronic recombination via tunneling between trapped electrons and recombination centers in luminescent materials. Recombination is assumed to take place from the excited state of the trapped electron to the nearest-neighbor center within a random distribution of luminescence recombination centers. Different possibilities are examined within the model, depending on the relative importance of electron de-excitation and recombination. The equations are applied to experimental TR-IRSL data of natural feldspars, and good agreement is found between experimental and modeling results.

  7. Microfluidic Leaching of Soil Minerals: Release of K+ from K Feldspar.

    PubMed

    Ciceri, Davide; Allanore, Antoine

    2015-01-01

    The rate of K+ leaching from soil minerals such as K-feldspar is believed to be too slow to provide agronomic benefit. Currently, theories and methods available to interpret kinetics of mineral processes in soil fail to consider its microfluidic nature. In this study, we measure the leaching rate of K+ ions from a K-feldspar-bearing rock (syenite) in a microfluidic environment, and demonstrate that at the spatial and temporal scales experienced by crop roots, K+ is available at a faster rate than that measured with conventional apparatuses. We present a device to investigate kinetics of mineral leaching at an unprecedented simultaneous resolution of space (~101-102 μm), time (~101-102 min) and fluid volume (~100-101 mL). Results obtained from such a device challenge the notion that silicate minerals cannot be used as alternative fertilizers for tropical soils.

  8. Microfluidic Leaching of Soil Minerals: Release of K+ from K Feldspar

    PubMed Central

    Ciceri, Davide; Allanore, Antoine

    2015-01-01

    The rate of K+ leaching from soil minerals such as K-feldspar is believed to be too slow to provide agronomic benefit. Currently, theories and methods available to interpret kinetics of mineral processes in soil fail to consider its microfluidic nature. In this study, we measure the leaching rate of K+ ions from a K-feldspar-bearing rock (syenite) in a microfluidic environment, and demonstrate that at the spatial and temporal scales experienced by crop roots, K+ is available at a faster rate than that measured with conventional apparatuses. We present a device to investigate kinetics of mineral leaching at an unprecedented simultaneous resolution of space (~101-102 μm), time (~101-102 min) and fluid volume (~100-101 mL). Results obtained from such a device challenge the notion that silicate minerals cannot be used as alternative fertilizers for tropical soils. PMID:26485160

  9. Age of K-feldspar authigenesis in Lower Paleozoic and uppermost Precambrian rocks of the Mississippi Valley area

    SciTech Connect

    Hay, R.L.; Liu, J. . Dept. of Geology); Deino, A. . Geochronology Center); Kyser, T.K. . Dept. of Geology)

    1992-01-01

    Published K-Ar dates (n = 12) of authigenic K-feldspar in Cambrian and Ordovician rocks of the Mississippi Valley area range from 448 to 375 Ma (Late Ordovician to Middle Devonian), suggesting a lengthy episode of K-feldspar authigenesis. Here the authors report an age span of 465--400 Ma (Middle Ordovician to Early Devonian) for authigenic K-feldspar of two samples from the alteration profile widely developed over Precambrian rocks at the unconformity with Cambrian deposits. This dating was done on 42 to 48 mesh grains of K-feldspar by the laser incremental-heating Ar-40/Ar-39 method. One sample, from west-central Wisconsin, is from a vein formed along a fracture in kaolinitic altered granite. Three grains nearest the fracture yielded plateau ages with a range of 9 Ma and an average of 430 Ma. Three grains distant from the fracture yielded a similar range of 10 Ma but with an average age of 397 Ma. Thus the grains grew over an extended period from at least 430 to 400 Ma. The other sample, from the St. Francois Mts. of Missouri, is of diabase replaced by K-feldspar. Three grains yielded plateau ages ranging over 20 Ma and apparently recording an extended history of K-feldspar growth. The average age of these grains is 454 Ma, compared to a K-Ar date of 444 [+-] 9 Ma obtained from a split of the same sample. The period(s) of K-feldspar authigenesis does not support its linkage with orogenic activity. Oxygen-isotope values of authigenic K-feldspar from lower Paleozoic and uppermost Precambrian rocks range from +19.8 to +23.0 [per thousand] and average 21.4 [per thousand] (N = 11). These values are compatible with formation of the K-feldspar from similar fluids and comparable temperatures.

  10. Crystal origins and magmatic system beneath Ngauruhoe volcano (New Zealand) revealed by plagioclase textures and compositions

    NASA Astrophysics Data System (ADS)

    Coote, Alisha C.; Shane, Phil

    2016-09-01

    The textural variation and compositional zoning of plagioclase in pre-historic and historic basaltic andesite lava flows from Ngauruhoe volcano reveals extensive crystal recycling from a multi-level magma system. Most phenocrysts have a calcic (~ An80-90) resorbed core with diffuse or no zonation that is depleted in Fe and Mg. Some cores display patchy zonation from replacement by high An crystallization prior to resorption. The cores are mantled by oscillatory-zoned rims of lower An content (< An60), and are enriched in Fe and Mg. Rim zones vary in relative thickness and textural complexity, and include sieve-textured bands, and/or cyclic calcic growth following dissolution events. A subordinate crystal population display similar features, but lack a resorbed core. These latter crystals display overall rimward enrichment in An, Fe and Mg. The resorbed cores crystallized from magmas more mafic than those erupted at Ngauruhoe, and slow cooling and prolonged storage resulted in loss of An zoning patterns and depletion of Fe and Mg by diffusion. These crystals are likely to have originated from deep cumulates or intrusions, and were subsequently entrained in ascending magmas. Patchy-textured cores were produced during decompression in a water under-saturated magma and staged ascent. The diversity in crystal cores reflect different conduits and ascent histories. The crystal rims grew in a more differentiated magma reservoir, and are in equilibrium with the erupted melt. Most of the zoning patterns in the rim zone require water pressure and/or temperature changes. These changes could have been caused by convective self-mixing in a closed system and/or the intrusion of hydrous melts of similar bulk composition. Other crystals display rimward elemental enrichments consistent with mafic recharge. Previously reported rimward enrichment in 87Sr-86Sr compositions can be explained by the re-cycled origin of the crystal cores and progressive crustal assimilation at shallower

  11. The effect of dynamic recrystallization and LPO formation on deformation mechanisms in experimentally deformed plagioclase aggregates

    NASA Astrophysics Data System (ADS)

    Meyers, C. D.; Hirth, G.; Cross, A. J.; Prior, D. J.

    2013-12-01

    We performed a series of deformation experiments on intermediate plagioclase aggregates (An60) that explored the role of dynamic recrystallization and LPO formation on the deformation mechanisms active and their effect on the mechanical strength of the aggregates. Our experiments were executed using a molten salt cell in a Tullis-modified Griggs Rig at 1 GPa, temperatures between 950-1100 C. These experiments were run in both axial compression and general shear geometries at both constant strain rates and with strain rate steps. The imposed strain rates ranged from 10^-4 to 5*10^-7 s^-1. The sample aggregates were prepared by sintering powders ranging from 20-45 micron at experimental P-T conditions prepared from pulverized single crystals of labradorite. We observed a strong dependence of strength on the strain-rate history of the experiment. Initially the samples weaken dramatically as the grain-size is reduced in the sample aggregate. During strain-rate stepping experiments, used to calculate the stress exponent, we observe variation in the strain-rate dependence of the strength related to whether there is an increasing or decreasing strain rate. Increasing the strain-rate tends to show stress exponent close to n=3, consistent with deformation by dislocation creep. Decreasing the strain-rate tends to decrease the stress exponent towards n=1, consistent with deformation by diffusion creep. Further, analysis using electron backscatter diffraction (EBSD) revealed distinctive LPOs that were different between larger relict porphryclast grains (>20 micron) and smaller recrystallized grains (1-4 micron). Larger relict grains have an LPO with {001} poles perpendicular to the shear plane, while smaller recrystallized grains have an LPO with {010} poles perpendicular to the shear plane. This is evidence that the processes that facilitate deformation are different between the relict and recrystallized grains. We also observe grain scale shear bands oriented roughly 30

  12. Diverse, Alkali-Rich Igneous and Volcaniclastic Rocks Reflect a Metasomatised Mantle Beneath Gale Crater

    NASA Astrophysics Data System (ADS)

    Schmidt, M. E.; Baker, M. B.; Berger, J. A.; Fisk, M. R.; Gellert, R.; McLennan, S. M.; Newcombe, M. E.; Stolper, E. M.; Thompson, L. M.

    2014-12-01

    Although Curiosity landed in a sedimentary setting, geochemical compositions determined by Alpha Particle X-ray Spectrometer (APXS) and ChemCam suggest that major element concentrations of some rocks were little modified by chemical weathering, and in these cases, the bulk (>70%) of the crystalline components determined by ChemMin are igneous. Gale rocks can therefore largely preserve the composition of their igneous protoliths and provide insight into the crystalline basement exposed in the north crater rim. Four end-member compositions are recognized on the basis of APXS analyses. (1) The diverse, evolved Jake M class (n=12) of inferred igneous origin includes float blocks and cobbles. Jake M rocks are phonotephritic/mugearitic to trachyandesitic and characterized by low MgO contents (3.0-5.7 wt%) and high Al and alkalis, particularly Na2O (up to 7.35 wt%). (2) The Bathurst class of siltstones to coarse sandstones (n=13) occurs as dark-toned float and bedded outcrop and is basaltic to trachybasaltic, ranging to high K2O (up to 3.8 wt%). Alteration of the protolith(s) or during diagenesis may have affected this class. (3) The Darwin class of conglomerates to coarse sandstones (n=10) has high Na and Al, likely reflecting a sodic plagioclase-rich mineralogy, but with higher Fe than Jake M class (13.0-17.1 vs. 6.0-12.5 wt%). (4) The low alkali "normal" Mars basaltic composition is typified by the Portage soils (n=6) and the John Klein class (n=13; includes the Sheepbed mudstone). Some degree of mixing and/or contamination with this low alkali basaltic compositon has affected all APXS analyses. Overall, Gale rocks are strongly enriched in total alkalis (at the same MgO) relative to basaltic shergottites and many have higher K2O than igneous rocks analyzed by Spirit and Opportunity, suggesting that the mantle beneath Gale is alkali-rich (likely as a result of a metasomatic event) and that alkalis are heterogeneously distributed in the planet's interior.

  13. Biochemical evolution. I. Polymerization on internal, organophilic silica surfaces of dealuminated zeolites and feldspars

    PubMed Central

    Smith, Joseph V.

    1998-01-01

    Catalysis at mineral surfaces might generate replicating biopolymers from simple chemicals supplied by meteorites, volcanic gases, and photochemical gas reactions. Many ideas are implausible in detail because the proposed mineral surfaces strongly prefer water and other ionic species to organic ones. The molecular sieve silicalite (Union Carbide; = Al-free Mobil ZSM-5 zeolite) has a three-dimensional, 10-ring channel system whose electrically neutral Si-O surface strongly adsorbs organic species over water. Three -O-Si tetrahedral bonds lie in the surface, and the fourth Si-O points inwards. In contrast, the outward Si-OH of simple quartz and feldspar crystals generates their ionic organophobicity. The ZSM-5-type zeolite mutinaite occurs in Antarctica with boggsite and tschernichite (Al-analog of Mobil Beta). Archean mutinaite might have become de-aluminated toward silicalite during hot/cold/wet/dry cycles. Catalytic activity of silicalite increases linearly with Al-OH substitution for Si, and Al atoms tend to avoid each other. Adjacent organophilic and catalytic Al-OH regions in nanometer channels might have scavenged organic species for catalytic assembly into specific polymers protected from prompt photochemical destruction. Polymer migration along weathered silicic surfaces of micrometer-wide channels of feldspars might have led to assembly of replicating catalytic biomolecules and perhaps primitive cellular organisms. Silica-rich volcanic glasses should have been abundant on the early Earth, ready for crystallization into zeolites and feldspars, as in present continental basins. Abundant chert from weakly metamorphosed Archaean rocks might retain microscopic clues to the proposed mineral adsorbent/catalysts. Other framework silicas are possible, including ones with laevo/dextro one-dimensional channels. Organic molecules, transition-metal ions, and P occur inside modern feldspars. PMID:9520372

  14. 40Ar/39Ar ages in deformed potassium feldspar: evidence of microstructural control on Ar isotope systematics

    NASA Astrophysics Data System (ADS)

    Reddy, Steven M.; Potts, Graham J.; Kelley, Simon P.

    2001-05-01

    Detailed field and microstructural studies have been combined with high spatial resolution ultraviolet laser 40Ar/39Ar dating of naturally deformed K-feldspar to investigate the direct relationship between deformation-related microstructure and Ar isotope systematics. The sample studied is a ~1,000 Ma Torridonian arkose from Skye, Scotland, that contains detrital feldspars previously metamorphosed at amphibolite-facies conditions ~1,700 Ma. The sample was subsequently deformed ~430 Ma ago during Caledonian orogenesis. The form and distribution of deformation-induced microstructures within three different feldspar clasts has been mapped using atomic number contrast and orientation contrast imaging, at a range of scales, to identify intragrain variations in composition and lattice orientation. These variations have been related to thin section and regional structural data to provide a well-constrained deformation history for the feldspar clasts. One hundred and forty-three in-situ 40Ar/39Ar analyses measured using ultraviolet laser ablation record a range of apparent ages (317-1030 Ma). The K-feldspar showing the least strain records the greatest range of apparent ages from 420-1,030 Ma, with the oldest apparent ages being found close to the centre of the feldspar away from fractures and the detrital grain boundary. The most deformed K-feldspar yields the youngest apparent ages (317-453 Ma) but there is no spatial relationship between apparent age and the detrital grain boundary. Within this feldspar, the oldest apparent ages are recorded from orientation domain boundaries and fracture surfaces where an excess or trapped 40Ar component resides. Orientation contrast images at a similar scale to the Ar analyses illustrate a significant deformation-related microstructural difference between the feldspars and we conclude that deformation plays a significant role in controlling Ar systematics of feldspars at both the inter- and intragrain scales even at relatively low

  15. Preparation of ultrafine silica from potash feldspar using sodium carbonate roasting technology

    NASA Astrophysics Data System (ADS)

    Liu, Jia-nan; Shen, Xiao-yi; Wu, Yan; Zhang, Jun; Zhai, Yu-chun

    2016-08-01

    A novel process was developed for the preparation of ultrafine silica from potash feldspar. In the first step, potash feldspar was roasted with Na2CO3 and was followed by leaching using NaOH solution to increase the levels of potassium, sodium, and aluminum in the solid residue. The leaching solution was then carbonated to yield ultrafine silica. The optimized reaction conditions in the roasting process were as follows: an Na2CO3-to-potash feldspar molar ratio of 1.1, a reaction temperature of 875°C, and a reaction time of 1.5 h. Under these conditions, the extraction rate of SiO2 was 98.13%. The optimized carbonation conditions included a final solution pH value of 9.0, a temperature of 40°C, a CO2 flow rate of 6 mL/min, a stirring intensity of 600 r/min, and an ethanol-to-water volume ratio of 1:9. The precipitation rate and granularity of the SiO2 particles were 99.63% and 200 nm, respectively. We confirmed the quality of the obtained ultrafine silica by comparing the recorded indexes with those specified in Chinese National Standard GB 25576―2010.

  16. Gamma activity of stream sediment feldspars as ceramic raw materials and their environmental impact.

    PubMed

    Aboelkhair, Hatem; Ibrahim, Tarek; Saad, Ahmed

    2012-08-01

    In situ gamma spectrometric measurements have been performed to characterise the natural radiation that emitted from the stream sediment feldspars in Wadi El Missikat and Wadi Homret El Gergab, Eastern Desert, Egypt. The measurements of potassium (K, %), equivalent uranium (eU, ppm) and equivalent thorium (eTh, ppm) were converted into specific activities and equivalent dose rate. The average specific activities were 1402 Bq kg(-1) for K, 113 Bq kg(-1) for eU and 108 Bq kg(-1) for eTh in Wadi El Missikat, while they were 1240, 104 and 185 Bq kg(-1) in Wadi Homret El Gergab. The calculated outdoor average effective dose rates was 1.1 mSv y(-1) in wadi El Missikat and 1.3 mSv y(-1) in Wadi Homret El Gergab. The terrestrial-specific activities and effective dose rate levels of the natural radioactivity in the two areas lie within the international recommended limits for occupational feldspar quarry workers. On the other hand, these results indicated that irradiation is higher than the allowable level for members of the public. Therefore, quarrying the feldspar sediments from these locations as ceramic raw materials may yield an undesired impact on the environment, especially through the indoor applications. PMID:22171098

  17. Sorption Mechanisms of Antibiotic Cephapirin onto Quartz and Feldspar by Raman Spectroscopy

    SciTech Connect

    Peterson, Jonathan; Wang, Wei; Gu, Baohua

    2009-01-01

    Raman spectroscopy was used to investigate the sorption mechanisms of cephapirin (CHP), a veterinary antibiotic, onto quartz (SiO2) and feldspar (KAlSi3O8) at different pH values. Depending on the charge and surface properties of the mineral, different reaction mechanisms including electrostatic attraction, monodentate and bidentate complexation were found to be responsible for CHP sorption. The zwitterion (CHPo) adsorbs to a quartz(+) surface by electrostatic attraction of the carboxylate anion group ( COO-) at a low pH, but adsorbs to a quartz(-) surface through electrostatic attraction of the pyridinium cation and possibly COO- bridge complexes at relatively higher pH conditions. CHP- bonds to a quartz(-) surface by bidentate complexation between one oxygen of COO- and oxygen from the carbonyl (C=O) of the acetoxymethyl group. On a feldspar surface of mixed charge, CHPo forms monodentate complexes between C=O as well as COO- bridging complexes or electrostatically attached to localized edge (hydr)oxy-Al surfaces. CHP- adsorbs to feldspar(-) through monodentate C=O complexation, and similar mechanisms may operate for the sorption of other cephalosporins. This research demonstrates, for the first time, that Raman spectroscopic techniques can be effective for evaluating the sorption processes and mechanisms of cephalosporin antibiotics even at relatively low sorbed concentrations (97-120 μmol/kg).

  18. Gamma activity of stream sediment feldspars as ceramic raw materials and their environmental impact.

    PubMed

    Aboelkhair, Hatem; Ibrahim, Tarek; Saad, Ahmed

    2012-08-01

    In situ gamma spectrometric measurements have been performed to characterise the natural radiation that emitted from the stream sediment feldspars in Wadi El Missikat and Wadi Homret El Gergab, Eastern Desert, Egypt. The measurements of potassium (K, %), equivalent uranium (eU, ppm) and equivalent thorium (eTh, ppm) were converted into specific activities and equivalent dose rate. The average specific activities were 1402 Bq kg(-1) for K, 113 Bq kg(-1) for eU and 108 Bq kg(-1) for eTh in Wadi El Missikat, while they were 1240, 104 and 185 Bq kg(-1) in Wadi Homret El Gergab. The calculated outdoor average effective dose rates was 1.1 mSv y(-1) in wadi El Missikat and 1.3 mSv y(-1) in Wadi Homret El Gergab. The terrestrial-specific activities and effective dose rate levels of the natural radioactivity in the two areas lie within the international recommended limits for occupational feldspar quarry workers. On the other hand, these results indicated that irradiation is higher than the allowable level for members of the public. Therefore, quarrying the feldspar sediments from these locations as ceramic raw materials may yield an undesired impact on the environment, especially through the indoor applications.

  19. Alkali-Metasomatism and Phyllonite Development Along a Major Alpine Shear Zone: the East Tenda Shear Zone (alpine Corsica, France)

    NASA Astrophysics Data System (ADS)

    Maggi, Matteo; Rossetti, Federico; Theye, Thomas

    2010-05-01

    Here we present results of an integrated study which combines structural geology, petrology and geochemistry addressed to assess modes and regimes of fluid-rock interaction during shear fabric development along the East Tenda Shear Zone (ETSZ), Haute Corse, France. This shear zone marks the overthrusting of the oceanic-derived Schistes Lustrés nappe onto the Hercynian granitic basement of the western Corsica. The granitic protolith (Casta Granodiorite) consists of K-feldspar, plagioclase, quartz and minor hornblende, and accessory apatite and zircon. A progressive, ductile-to-brittle top-to-the-W/SW shearing affects the Casta granodiorite, evolving from blueschist-facies (S-L tectonites) to upper crustal (brittle thrust faults) conditions. Apart the variably retrogressed mafic blueschist boudins, within the ETSZ two main rock types were recognised: weakly-foliated gneisses (hereafter referred as massive bodies) and phengite-dominated mylonites (hereafter referred as phyllonites). Both rock types consist of a high-variance mineral assemblage made up of feldspar (albite and K-feldspar) + quartz + phengite. Accessory minerals include relict zircons, and syn-kinematic andradite, epidote, monazite, leucoxene and titanite. At a regional scale, phyllonites envelop the massive bodies that, commonly, form sigma-shaped shear lenses wrapped within the mylonitic foliation. Phyllonites consist of alternating, micro-crystalline quartz-feldspar-phengite-bearing layers and by different generation of variably deformed quartz and composite quartz-feldspar (albite and microcline) vein segregations (up to 30 cm in thickness). Late-stage, laminated sub-horizontal quartz-feldspar vein arrays also occur, suggesting their origin as thrust-related shear veins. Microtextures are indicative of pseudomorphic growth of phengite after relict igneous K-feldspar. Nevertheless, new growth of microcline is ubiquitous along the rims of porphyroclastic K-feldspar grains. EMPA of phengite

  20. The alkali metals: 200 years of surprises.

    PubMed

    Dye, James L

    2015-03-13

    Alkali metal compounds have been known since antiquity. In 1807, Sir Humphry Davy surprised everyone by electrolytically preparing (and naming) potassium and sodium metals. In 1808, he noted their interaction with ammonia, which, 100 years later, was attributed to solvated electrons. After 1960, pulse radiolysis of nearly any solvent produced solvated electrons, which became one of the most studied species in chemistry. In 1968, alkali metal solutions in amines and ethers were shown to contain alkali metal anions in addition to solvated electrons. The advent of crown ethers and cryptands as complexants for alkali cations greatly enhanced alkali metal solubilities. This permitted us to prepare a crystalline salt of Na(-) in 1974, followed by 30 other alkalides with Na(-), K(-), Rb(-) and Cs(-) anions. This firmly established the -1 oxidation state of alkali metals. The synthesis of alkalides led to the crystallization of electrides, with trapped electrons as the anions. Electrides have a variety of electronic and magnetic properties, depending on the geometries and connectivities of the trapping sites. In 2009, the final surprise was the experimental demonstration that alkali metals under high pressure lose their metallic character as the electrons are localized in voids between the alkali cations to become high-pressure electrides!

  1. The alkali metals: 200 years of surprises.

    PubMed

    Dye, James L

    2015-03-13

    Alkali metal compounds have been known since antiquity. In 1807, Sir Humphry Davy surprised everyone by electrolytically preparing (and naming) potassium and sodium metals. In 1808, he noted their interaction with ammonia, which, 100 years later, was attributed to solvated electrons. After 1960, pulse radiolysis of nearly any solvent produced solvated electrons, which became one of the most studied species in chemistry. In 1968, alkali metal solutions in amines and ethers were shown to contain alkali metal anions in addition to solvated electrons. The advent of crown ethers and cryptands as complexants for alkali cations greatly enhanced alkali metal solubilities. This permitted us to prepare a crystalline salt of Na(-) in 1974, followed by 30 other alkalides with Na(-), K(-), Rb(-) and Cs(-) anions. This firmly established the -1 oxidation state of alkali metals. The synthesis of alkalides led to the crystallization of electrides, with trapped electrons as the anions. Electrides have a variety of electronic and magnetic properties, depending on the geometries and connectivities of the trapping sites. In 2009, the final surprise was the experimental demonstration that alkali metals under high pressure lose their metallic character as the electrons are localized in voids between the alkali cations to become high-pressure electrides! PMID:25666067

  2. Process for the disposal of alkali metals

    DOEpatents

    Lewis, Leroy C.

    1977-01-01

    Large quantities of alkali metals may be safely reacted for ultimate disposal by contact with a hot concentrated caustic solution. The alkali metals react with water in the caustic solution in a controlled reaction while steam dilutes the hydrogen formed by the reaction to a safe level.

  3. Method of handling radioactive alkali metal waste

    DOEpatents

    Wolson, R.D.; McPheeters, C.C.

    Radioactive alkali metal is mixed with particulate silica in a rotary drum reactor in which the alkali metal is converted to the monoxide during rotation of the reactor to produce particulate silica coated with the alkali metal monoxide suitable as a feed material to make a glass for storing radioactive material. Silica particles, the majority of which pass through a 95 mesh screen or preferably through a 200 mesh screen, are employed in this process, and the preferred weight ratio of silica to alkali metal is 7 to 1 in order to produce a feed material for the final glass product having a silica to alkali metal monoxide ratio of about 5 to 1.

  4. Method of handling radioactive alkali metal waste

    DOEpatents

    Wolson, Raymond D.; McPheeters, Charles C.

    1980-01-01

    Radioactive alkali metal is mixed with particulate silica in a rotary drum reactor in which the alkali metal is converted to the monoxide during rotation of the reactor to produce particulate silica coated with the alkali metal monoxide suitable as a feed material to make a glass for storing radioactive material. Silica particles, the majority of which pass through a 95 mesh screen or preferably through a 200 mesh screen, are employed in this process, and the preferred weight ratio of silica to alkali metal is 7 to 1 in order to produce a feed material for the final glass product having a silica to alkali metal monoxide ratio of about 5 to 1.

  5. Crystallization temperature determination of Itokawa particles by plagioclase thermometry with X-ray diffraction data obtained by a high-resolution synchrotron Gandolfi camera

    NASA Astrophysics Data System (ADS)

    Tanaka, Masahiko; Nakamura, Tomoki; Noguchi, Takaaki; Nakato, Aiko; Ishida, Hatsumi; Yada, Toru; Shirai, Kei; Fujimura, Akio; Ishibashi, Yukihiro; Abe, Masanao; Okada, Tatsuaki; Ueno, Munetaka; Mukai, Toshifumi

    2014-02-01

    The crystallization temperatures of Itokawa surface particles recovered by the space probe Hayabusa were estimated by a plagioclase geothermometer using sodic plagioclase triclinicity. The Δ131-index required for the thermometer, which is the difference in X-ray diffraction peak positions between the 131 and 13¯1 reflections of plagioclase, was obtained by a high-resolution synchrotron Gandolfi camera developed for the third generation synchrotron radiation beamline, BL15XU at SPring-8. Crystallization temperatures were successfully determined from the Δ131-indices for four particles. The observed plagioclase crystallization temperatures were in a range from 655 to 660 °C. The temperatures indicate crystallization temperatures of plagioclases in the process of prograde metamorphism before the peak metamorphic stage.

  6. Age and thermochronology of K-feldspars from the Manson Impact Structure

    NASA Technical Reports Server (NTRS)

    Zeitler, P. K.; Kunk, M. J.

    1993-01-01

    As a contribution to the effort to obtain a precise age for the Manson Impact Structure, we are approaching the problem from a thermo chronological perspective, with the goal of extracting an age from Ar-40/Ar-39 age-spectrum analysis of partially overprinted K-feldspars taken from granitoid clasts. We find that shocked feldspars from Manson generally show a strong overprint in their age spectra, with more than 50 percent of each spectrum being reset. The reset portions of the age spectra correspond to gas lost from very small diffusion domains, and a characteristic of the Manson samples is the very large range in apparent diffusion dimensions that they display, with the smallest domains being some 400 times smaller than the largest domains. It is also noteworthy that the small domains comprise a substantial portion of the volume of the feldspars (50 percent or more). These observations are consistent with the extreme shock experienced by these samples. In detail, the spectra we have measured to date are saddle-shaped and show minimum ages of between 67 and 72 Ma, which we interpret to be maximum estimates for the age of the impact. In the case of one sample (M1-678.3; K-feldspar from a large syenite block located well below the apparent melt-matrix breccia in the M1 borehole), isotope correlation analysis suggests the presence of a non-atmospheric trapped Ar component (Ar-40/Ar-36 of 660 plus or minus 40), and an age of about 65.3 plus or minus 0.5 Ma (2 sigma). Our interpretation of our results is that the shock of impact greatly reduced the diffusion-domain sizes of our samples, making them susceptible to significant Ar loss during heating associated with impact. It appears that while our feldspars were partially open to Ar loss, they equilibrated with a non-atmospheric Ar component, probably related to impact-related degassing of old basement around the impact site.

  7. Microtextural Study of Feldspar in Petrologic Type 3 LL Ordinary Chondrites: A Record of Parent Body Metasomatism

    NASA Astrophysics Data System (ADS)

    Lewis, J. A.; Jones, R. H.

    2014-09-01

    We have carried out a detailed study of LL3 ordinary chondrites, focusing on the chemical and microtextural development of feldspar, to help understand the low-temperature evolution of the LL parent body(ies).

  8. Oxygen isotope heterogeneity of arc magma recorded in plagioclase from the 2010 Merapi eruption (Central Java, Indonesia)

    NASA Astrophysics Data System (ADS)

    Borisova, Anastassia Y.; Gurenko, Andrey A.; Martel, Caroline; Kouzmanov, Kalin; Cathala, Annick; Bohrson, Wendy A.; Pratomo, Indyo; Sumarti, Sri

    2016-10-01

    Chemical and isotopic compositions of magmatic crystals provide important information to distinguish between deep juvenile and crustal contributions. In this work, high-resolution multicollector secondary ion mass spectrometry data reveal strong variations of δ18O values in three plagioclase crystals (800-1700 μm) from two representative basaltic andesite samples of the 2010 Merapi eruption (Central Java, Indonesia). The δ18O values (from 4.6‰ to 7.9‰) are interpreted to reflect oxygen isotope heterogeneity in the melt composition during plagioclase growth. The lowest δ18O values (4.6-6.6‰) are found in anorthite-rich cores (An82-97), whereas higher δ18O values (5.7-7.9‰) are found in anorthite-poorer zones (An33-86), typically in crystal rims. Combining these new plagioclase δ18O data with δ18O of calc-silicate crustal xenoliths erupted between 1994 and 1998, the composition of glass inclusions hosted by the anorthite-rich plagioclase (An82-92), available experimental data, and the results of thermodynamic modeling using the Magma Chamber Simulator code, we conclude that the abundant anorthite-rich cores crystallized from a mantle-derived hydrous basaltic to basaltic trachyandesite melt that recharged a deeper (200-600 MPa) magma storage zone, whereas lower anorthite zones crystallized at shallower levels (100-200 MPa). The oxygen isotope variations in the plagioclase are explained by a two-stage model of interaction of the hydrous, mafic mantle-derived magma (1) with old crustal rocks depleted in 18O due to high temperature alteration that yielded the low δ18O values in the anorthite-rich cores at deep levels (13-20 km), and later (2) with 18O-enriched carbonate material that yielded the high δ18O values in anorthite-poorer zones at shallow levels (∼4.5-9 km). Thermodynamic modeling is consistent with ∼18 wt.% assimilation of crustal calc-silicate material at 925-950 °C and 100-200 MPa by the 2010 Merapi basaltic andesite magma prior to

  9. Comment on “Systematic variations of argon diffusion in feldspars and implications for thermochronometry” by Cassata and Renne

    NASA Astrophysics Data System (ADS)

    Lovera, Oscar M.; Harrison, T. Mark; Boehnke, Patrick

    2015-02-01

    Cassata and Renne (2013) is a data-rich paper potentially providing opportunities to systematically test long-standing models of argon diffusion behavior in feldspars and we congratulate them on a heroic achievement. That said, several of their interpretations are highly problematic due to misconceptions of both the nature of their sample and diffusion modeling. Evidence of grain-scale diffusion in an exsolved feldspar

  10. AUthigenic feldspar as an indicator of paleo-rock/water interactions in Permian carbonates of the Northern Calcareous Alps, Austria

    USGS Publications Warehouse

    Spotl, C.; Kralik, M.; Kunk, M.J.

    1996-01-01

    Dolostones interbedded with Upper Permian evaporites at the base of the Northern Calcareous Alps contain abundant authigenic K-feldspar. Two petrographically, structurally, and isotopically distinct generations of K-feldspar can be distinguished: crystals composed of an inclusion-rich core and a clear rim, and optically unzoned, transparent crystals. Both feldspar types have essentially identical K-feldspar end-member compositions with ??? 99.5 mole % Or component. Low oxygen isotope ratios (+16.1??? to +18.1??? SMOW) suggest precipitation from 18O-enriched, saline fluids at temperatures in excess of ??? 140??C. 40Ar/39Ar plateau-age spectra of five samples range from 145 ?? 1 to 144 ?? 1 Ma (Early Berriasian) and suggest that both types of feldspar were formed within an interval that did not exceed ??? 2 m.y. Rb/Sr model ages range from 152 to 140 Ma, assuming that the burial diagenetic regime was buffered with respect to strontium by the associated marine Permian evaporites. Authigenic K-feldspar records two distinct events of hot brine flow, most likely triggered by tectonic movements (detachment) and by an increase in the subsurface temperature in response to thrust loading.

  11. Authigenic feldspar as an indicator of paleo-rock/water interactions in Permian carbonates of the Northern Calcareous Alps, Austria

    SciTech Connect

    Spoetl, C.; Kralik, M.; Kunk, M.J.

    1996-01-01

    Dolostones interbedded with Upper Permian evaporites at the base of the Northern Calcareous alps contain abundant authigenic K-feldspar. Two petrographically, structurally, and isotopically distinct generations of K-feldspar can be distinguished: crystals composed of an inclusion-rich core and a clear rim, and optically unzoned, transparent crystals. Both feldspar types have essentially identical K-feldspar end-member compositions with {ge} 99.5 mole % Or component. Low oxygen isotope ratios (+16.1{per_thousand} to + 18.1{per_thousand} SMOW) suggest precipitation from {sup 18}O-enriched, saline fluids at temperatures in excess of {approximately} 140 C. {sup 40}Ar/{sup 39}Ar plateau-age spectra of five samples range from 145 {+-} 1 to 144 {+-} 1 Ma (Early Berriasian) and suggest that both types of feldspar were formed within an interval that did not exceed {approximately} 2 m.y. Rb/Sr model ages range from 152 to 140 Ma, assuming that the burial diagenetic regime was buffered with respect to strontium by the associated marine Permian evaporites. Authigenic K-feldspar records two distinct events of hot brine flow, most likely triggered by tectonic movements (detachment) and by an increase in the subsurface temperature in response to thrust loading.

  12. Surface chemistry of labradorite feldspar reacted with aqueous solutions at pH = 2, 3, and 12

    NASA Astrophysics Data System (ADS)

    Casey, William H.; Westrich, Henry R.; Arnold, George W.

    1988-12-01

    The reaction of feldspar with an aqueous solution is examined by complementing dissolution rate measurements with analysis of mineral surface chemistry. Rates of feldspar dissolution were measured in H 2O - HCl and D 2O - DCl solutions. These measurements were combined with elastic recoil detection (ERD) analysis of hydrogen isotope concentration, and Rutherford backscattering analysis (RBS) of silicon, aluminum and calcium concentrations near the surface of the mineral. Dissolution rates of labradorite feldspar in H 2O - HCl solutions ( pH = 1.7) are 33% more rapid than in D 2O - DCl mixtures ( pD = 1.7). The depth of penetration and inventory of hydrogen in the feldspar is a strong function of solution pH, temperature, and reaction time. Hydrogen infiltrates the feldspar more extensively from an acidic solution than from a basic solution, and complete isotopic exchange between the hydration layer and water proceeds in time on the order of hours. The hydrolysis of bridging Si - O - Al bonds by reaction with a strongly acidic solution for several hundreds of hours progresses to depths of several hundreds of Angstroms into the mineral. Calcium is also removed from the mineral to this depth during reaction with an acidic solution. The composition of the reacted surface, however, cannot be explained solely on the basis of ion exchange or depolymerization reactions. The data suggest that the silicon-rich surface of feldspar continually repolymerizes during reaction, and that this repolymerization eliminates hydrogen from the hydration layer.

  13. Measurement of alkali in PFBC exhaust

    SciTech Connect

    Lee, S.H.D.; Swift, W.M.

    1992-11-01

    This project supports the DOE/METC Fossil Energy Program for the development of PFBC technology. Based on the analytical activated-bauxite sorber-bed technique, we are developing the RABSAM as an altemative to the on-line alkali analyzer for field application. As shown in Fig. 1, the RABSAM is a sampling probe containing a regenerable activated-bauxite adsorbent (RABA). It can be inserted directly into the PFBC exhaust duct and requires no HTHP sampling line. Alkali vapors are captured by the adsorbent purely through physical adsorption. The adsorbent is regenerated by a simple water-leaching process, which also recovers the adsorbed alkalis. The alkali analysis of the leachate by atomic absorption (AA) provides a basis for calculating the time-averaged alkali-vapor concentration in the PFBC exhaust. If the RABA is to use commercial grade activated bauxite, the clay impurities in activated bauxite can react with alkali vapors and, therefore, need to be either removed or deactivated. In earlier work, a 6M-LiCl-solution impregnation technique was shown to deactivate these impurities in fresh activated bauxite [8]. During this year, RABA prepared by this technique was tested in a pressurized alkali-vapor sorption test unit to determine its NaCl-vapor capture efficiency and the regenerability of the sorbent by water extraction. Results of this study are presented and discussed.

  14. Measurement of alkali in PFBC exhaust

    SciTech Connect

    Lee, S.H.D.; Swift, W.M.

    1992-01-01

    This project supports the DOE/METC Fossil Energy Program for the development of PFBC technology. Based on the analytical activated-bauxite sorber-bed technique, we are developing the RABSAM as an altemative to the on-line alkali analyzer for field application. As shown in Fig. 1, the RABSAM is a sampling probe containing a regenerable activated-bauxite adsorbent (RABA). It can be inserted directly into the PFBC exhaust duct and requires no HTHP sampling line. Alkali vapors are captured by the adsorbent purely through physical adsorption. The adsorbent is regenerated by a simple water-leaching process, which also recovers the adsorbed alkalis. The alkali analysis of the leachate by atomic absorption (AA) provides a basis for calculating the time-averaged alkali-vapor concentration in the PFBC exhaust. If the RABA is to use commercial grade activated bauxite, the clay impurities in activated bauxite can react with alkali vapors and, therefore, need to be either removed or deactivated. In earlier work, a 6M-LiCl-solution impregnation technique was shown to deactivate these impurities in fresh activated bauxite [8]. During this year, RABA prepared by this technique was tested in a pressurized alkali-vapor sorption test unit to determine its NaCl-vapor capture efficiency and the regenerability of the sorbent by water extraction. Results of this study are presented and discussed.

  15. Alkali metasomatism in the major gneiss, northwest Adirondacks, New York: open system or closed?

    NASA Astrophysics Data System (ADS)

    Carl, James D.

    1981-09-01

    The thickest clastic unit in the northwest Adirondacks. New York, undergoes gradual transition from amphibolite to granulite facies over a distance of 55 km from Emeryville to Colton. This Precambrian quartz-biotite-oligoclase-K-feldspar gneiss with migmatite characteristics has long been cited as having undergone progressive loss of K, Si, Fe2+, Ba and H2O toward Colton and granulite facies conditions (ENGEL and ENGEL, 1958, 1960a. b). Chemical data obtained from new samples, however, cast doubt upon the interpretation of open system alkali metasomatism. Outcrop to outcrop chemical variation is shown to be of similar magnitude to the chemical variation recorded across the entire gneiss belt. Chemical differences between Emeryville and Colton are not those expected from progressive degranitization by loss of alkali-bearing fluid. Ratios of {K}/{Rb} and Ca-Na K suggest that metamorphism was isochemical on the scale of outcrop. These new data were obtained from mixtures of leucosome and fine-grained paragneiss at each of 7 outcrops. The sampling technique contrasts with that of A.E.J. and C. Engel who analyzed leucosome separately from fine grained (‘least altered’) gneiss.

  16. Preferred lattice orientations of plagioclase from amphibolite and greenschist facies rocks near the Insubric Line (Western Alps)

    NASA Astrophysics Data System (ADS)

    Kruhl, Jörn H.

    1987-04-01

    Preferred lattice orientations of plagioclase, measured by the universal stage, from deformed amphibolite and greenschist facies rocks near the Insubric Line (Western Alps), reflect the type and orientation of the strain system: either (001) or (010) are oriented parallel or subparallel to the schistosity and form more or less complete girdles around the stretching direction. By the preferred orientation patterns dominant (010) [001] slip is indicated and, additionally, slip on (001) parallel to the a direction, possibly at somewhat higher temperatures and/or at a higher An content of the plagioclase. It is suggested that obliquities of the symmetry-planes of the orientation patterns against the principle axes of strain are related to the sense of shearing.

  17. Diode pumped alkali vapor fiber laser

    DOEpatents

    Payne, Stephen A.; Beach, Raymond J.; Dawson, Jay W.; Krupke, William F.

    2007-10-23

    A method and apparatus is provided for producing near-diffraction-limited laser light, or amplifying near-diffraction-limited light, in diode pumped alkali vapor photonic-band-gap fiber lasers or amplifiers. Laser light is both substantially generated and propagated in an alkali gas instead of a solid, allowing the nonlinear and damage limitations of conventional solid core fibers to be circumvented. Alkali vapor is introduced into the center hole of a photonic-band-gap fiber, which can then be pumped with light from a pump laser and operated as an oscillator with a seed beam, or can be configured as an amplifier.

  18. Diode pumped alkali vapor fiber laser

    DOEpatents

    Payne, Stephen A.; Beach, Raymond J.; Dawson, Jay W.; Krupke, William F.

    2006-07-26

    A method and apparatus is provided for producing near-diffraction-limited laser light, or amplifying near-diffraction-limited light, in diode pumped alkali vapor photonic-band-gap fiber lasers or amplifiers. Laser light is both substantially generated and propagated in an alkali gas instead of a solid, allowing the nonlinear and damage limitations of conventional solid core fibers to be circumvented. Alkali vapor is introduced into the center hole of a photonic-band-gap fiber, which can then be pumped with light from a pump laser and operated as an oscillator with a seed beam, or can be configured as an amplifier.

  19. Alkali Silicate Vehicle Forms Durable, Fireproof Paint

    NASA Technical Reports Server (NTRS)

    Schutt, John B.; Seindenberg, Benjamin

    1964-01-01

    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.

  20. Advancements in flowing diode pumped alkali lasers

    NASA Astrophysics Data System (ADS)

    Pitz, Greg A.; Stalnaker, Donald M.; Guild, Eric M.; Oliker, Benjamin Q.; Moran, Paul J.; Townsend, Steven W.; Hostutler, David A.

    2016-03-01

    Multiple variants of the Diode Pumped Alkali Laser (DPAL) have recently been demonstrated at the Air Force Research Laboratory (AFRL). Highlights of this ongoing research effort include: a) a 571W rubidium (Rb) based Master Oscillator Power Amplifier (MOPA) with a gain (2α) of 0.48 cm-1, b) a rubidium-cesium (Cs) Multi-Alkali Multi-Line (MAML) laser that simultaneously lases at both 795 nm and 895 nm, and c) a 1.5 kW resonantly pumped potassium (K) DPAL with a slope efficiency of 50%. The common factor among these experiments is the use of a flowing alkali test bed.

  1. Investigating K-feldspar Luminescence Thermochronometry for Application in the Mont Blanc Massif

    NASA Astrophysics Data System (ADS)

    Lambert, R.; King, G. E.; Herman, F.; Valla, P.

    2015-12-01

    Luminescence dating has the potential to quantify the recent exhumation history of mountain ranges as a low-temperature thermochronometer. During rock exhumation, electrons get trapped through exposure to ionizing radiation whilst elevated temperatures cause thermally stimulated detrapping. The resulting luminescence signals measured in the laboratory can be used to constrain rock thermal histories through modelling of the kinetic parameters of electron trapping and detrapping. Here, we investigate and model laboratory kinetic processes of the luminescence of K-feldspar and assess their extrapolation over geological timescales. Samples were taken from the actively eroding Mont Blanc massif in the European Alps, along a 12 km long tunnel with ambient temperatures of 10-35 °C. In this setting rapid exhumation rates have been found during the last 2 million years (up to ~2 km/Myr), however, we intend to increase the temporal resolution to sub-Quaternary timescales using luminescence thermochronometry. Infra-red stimulated luminescence signals at 50 °C (IR50) and at 225 °C (post-IR IRSL225) of K-feldspar extracted from Mont Blanc tunnel samples were measured and our first results reveal a thermal signature from which rock cooling rates can be derived. Isothermal decay experiments show non-exponential decay, but interestingly, experiments with a range of regenerative doses reveal first-order kinetics. The observed thermal decay pattern is well-described by a model based on a physically plausible distribution of the density of states. Ultimately, we intend to use the IR50 and post-IR IRSL225 signals of K-feldspar as dual thermochronometers to determine the late-Quaternary cooling history of the Mont Blanc massif. Moreover, the luminescence signals may give insights into local thermal field evolution, before the influence of postglacial hydrothermal flow.

  2. Spectral variability of plagioclase-mafic mixtures (1): Effects of chemistry and modal abundance in reflectance spectra of rocks and mineral mixtures

    NASA Astrophysics Data System (ADS)

    Serventi, Giovanna; Carli, Cristian; Sgavetti, Maria; Ciarniello, Mauro; Capaccioni, Fabrizio; Pedrazzi, Giuseppe

    2013-09-01

    Remote sensing from lunar highland and from Hermean surface showed reflectance spectra with no detectable absorption bands in the visible and near infrared, and recently M3 data from the lunar surface (e.g., Orientale Basin) have shown spectra with a weak absorption band centered at 1250 nm. Those terrains were generally interpreted as plagioclase rich regions. Plagioclase, however, has often been considered a spectrally transparent and almost featureless mineral. So it is difficult to recognize its presence and to quantify the abundance of this mineral even if it is one of the most important mineralogical component of the planetary surfaces. In this work we investigate the influence of plagioclase absorption band on the absorption of Fe, Mg minerals. We consider three plagioclases with different FeO wt.% contents which have been mixed with three mafic end-members (1) pyroxene-bearing and olivine-free, (2) olivine-poor and (3) olivine-rich, at two different grain size. Plagioclase’s influence has been expressed considering variation of different spectral parameters: band position, band intensity and band width. We show that plagioclase has spectroscopically different behavior when mixed with olivine-bearing or olivine-free end-members, but, in general, adding modal abundance of plagioclase produces higher albedo and reduced spectral contrast. Increasing FeO content in plagioclase and coarsening the grain size have similar effects on the mixture spectra. We also observed the spectral convergence of mixtures with different composition and grain size. With these results, we point out the importance of considering the plagioclase absorption on mixture’s mineralogical composition, when spectra from different terrain are considered. Moreover, accurate evaluation of the abundance of plagioclase in those mixture should be discussed in subsequent works.

  3. Alkali metal for ultraviolet band-pass filter

    NASA Technical Reports Server (NTRS)

    Mardesich, Nick (Inventor); Fraschetti, George A. (Inventor); Mccann, Timothy A. (Inventor); Mayall, Sherwood D. (Inventor); Dunn, Donald E. (Inventor); Trauger, John T. (Inventor)

    1993-01-01

    An alkali metal filter having a layer of metallic bismuth deposited onto the alkali metal is provided. The metallic bismuth acts to stabilize the surface of the alkali metal to prevent substantial surface migration from occurring on the alkali metal, which may degrade optical characteristics of the filter. To this end, a layer of metallic bismuth is deposited by vapor deposition over the alkali metal to a depth of approximately 5 to 10 A. A complete alkali metal filter is described along with a method for fabricating the alkali metal filter.

  4. Effect of ageing of K-feldspar on its ice nucleating efficiency in immersion, deposition and contact freezing modes

    NASA Astrophysics Data System (ADS)

    Peckhaus, Andreas; Bachmann, Felix; Hoffmann, Nadine; Koch, Michael; Kiselev, Alexei; Leisner, Thomas

    2015-04-01

    Recently K-feldspar was identified as one of the most active atmospheric ice nucleating particles (INP) of mineral origin [1]. Seeking the explanation to this phenomena we have conducted extensive experimental investigation of the ice nucleating efficiency of K-feldspar in three heterogeneous freezing modes. The immersion freezing of K-feldspar was investigated with the cold stage using arrays of nanoliter-size droplets containing aqueous suspension of polydisperse feldspar particles. For contact freezing, the charged droplets of supercooled water were suspended in the laminar flow of the DMA-selected feldspar-containing particles, allowing for determination of freezing probability on a single particle-droplet contact [2]. The nucleation and growth of ice via vapor deposition on the crystalline surfaces of macroscopic feldspar particles have been investigated in the Environmental Scanning Electron Microscope (ESEM) under humidified nitrogen atmosphere. The ice nucleation experiments were supplemented with measurements of effective surface area of feldspar particles and ion chromatography (IC) analysis of the leached framework cations (K+, Na+, Ca2+, Mg2+). In this contribution we focus on the role of surface chemistry influencing the IN efficiency of K-feldspar, in particular the connection between the degree of surface hydroxylation and its ability to induce local structural ordering in the interfacial layer in water molecules (as suggested by recent modeling efforts). We mimic the natural process of feldspar ageing by suspending it in water or weak aqueous solution of carbonic acid for different time periods, from minutes to months, and present its freezing efficiency as a function of time. Our immersion freezing experiments show that ageing have a nonlinear effect on the freezing behavior of feldspar within the investigated temperature range (-40°C to -10°C). On the other hand, deposition nucleation of ice observed in the ESEM reveals clear different pattern

  5. Alkali Metal Salts with Designable Aryltrifluoroborate Anions.

    PubMed

    Iwasaki, Kazuki; Yoshii, Kazuki; Tsuzuki, Seiji; Matsumoto, Hajime; Tsuda, Tetsuya; Kuwabata, Susumu

    2016-09-01

    Aryltrifluoroborate ([ArBF3](-)) has a designable basic anion structure. Various [ArBF3](-)-based anions were synthesized to create novel alkali metal salts using a simple and safe process. Nearly 40 novel alkali metal salts were successfully obtained, and their physicochemical characteristics, particularly their thermal properties, were elucidated. These salts have lower melting points than those of simple inorganic alkali halide salts, such as KCl and LiCl, because of the weaker interactions between the alkali metal cations and the [ArBF3](-) anions and the anions' larger entropy. Moreover, interestingly, potassium cations were electrochemically reduced in the potassium (meta-ethoxyphenyl)trifluoroborate (K[m-OEtC6H4BF3]) molten salt at 433 K. These findings contribute substantially to furthering molten salt chemistry, ionic liquid chemistry, and electrochemistry. PMID:27510799

  6. Alkali Metal Handling Practices at NASA MSFC

    NASA Technical Reports Server (NTRS)

    Salvail, Patrick G.; Carter, Robert R.

    2002-01-01

    NASA Marshall Space Flight Center (MSFC) is NASA s principle propulsion development center. Research and development is coordinated and carried out on not only the existing transportation systems, but also those that may be flown in the near future. Heat pipe cooled fast fission cores are among several concepts being considered for the Nuclear Systems Initiative. Marshall Space Flight Center has developed a capability to handle high-purity alkali metals for use in heat pipes or liquid metal heat transfer loops. This capability is a low budget prototype of an alkali metal handling system that would allow the production of flight qualified heat pipe modules or alkali metal loops. The processing approach used to introduce pure alkali metal into heat pipe modules and other test articles are described in this paper.

  7. Plagioclase and pyroxene hosted melt inclusions in basaltic andesites of the current eruption of Arenal volcano, Costa Rica

    NASA Astrophysics Data System (ADS)

    Streck, Martin J.; Wacaster, Sue

    2006-09-01

    In this study, we investigated melt inclusions hosted in pyroxene and plagioclase to find direct evidence for the composition of melt components in the pre-eruptive magmas of the current eruption of Arenal volcano and to further shed light on the petrogenetic history of remarkably uniform basaltic andesitic bulk compositions. Composition of melt inclusions ranges widely regardless of whether an inclusion is hosted by plagioclase or by pyroxene and whether crystals with inclusions came from tephra samples or from slower emplaced lava flows. However, inclusions from each type of host mineral have distinct evolutionary trends most consistent with being mainly introduced by post-emplacement crystallization of the enclosing host, which is also supported by the composition of groundmass glasses. At the least-modified compositions, plagioclase and pyroxene inclusion trends overlap allowing for identification of melt compositions entrapped by both phases and, thus, strongly suggesting that these melt compositions existed in the reservoir prior to entrapment. Most of these are "dacitic" (61 to 64 wt.% SiO 2) and strongly match phenocryst-poor dacitic magmas of earlier eruptive phases of Arenal [Borgia, A., Poore, C., Carr, M.J., Melson, W.G., Alvarado, G.E., 1988. Structural, stratigraphic, and petrologic aspects of the Arenal-Chato volcanic system, Costa Rica: evolution of a young stratovolcanic complex. Bull Volcanol, 50, 86-105], suggesting earlier dacitic magmas may have been generated by melt-extraction processes. Correction for host crystallization of some inclusions also suggests that melt components as mafic as ˜ 53 wt.% may have been entrapped. All melt components inferred to have existed in the magmatic reservoirs prior to entrapment have low Mg# (38-45) yielding evidence for liquid compositions required for crystallizing the bulk of observed pyroxene and likely also olivine. Water rich (> 5 wt.%, by difference) and probably undegassed (S = 400-1600 ppm, Cl =

  8. Desulfurizing Coal With an Alkali Treatment

    NASA Technical Reports Server (NTRS)

    Ravindram, M.; Kalvinskas, J. J.

    1987-01-01

    Experimental coal-desulfurization process uses alkalies and steam in fluidized-bed reactor. With highly volatile, high-sulfur bituminous coal, process removed 98 percent of pyritic sulfur and 47 percent of organic sulfur. Used in coal liquefaction and in production of clean solid fuels and synthetic liquid fuels. Nitrogen or steam flows through bed of coal in reactor. Alkalies react with sulfur, removing it from coal. Nitrogen flow fluidizes bed while heating or cooling; steam is fluidizing medium during reaction.

  9. Age of authigenic K-feldspar in Lower Paleozoic and uppermost Precambrian rocks of the Mississippi Valley area

    SciTech Connect

    Hay, R.L.; Liu, J. . Dept. of Geology); Deino, A. . Geochronology Center); Kyser, T.K. . Dept. of Geology)

    1993-03-01

    Published K-Ar dates of authigenic K-feldspar in Cambrian and Ordovician rocks of the Mississippi Valley area range from 448 to 375 Ma (Late Ordovician to Middle Devonian), suggesting a lengthy episode of K-feldspar authigenesis. Here the authors report an age span of [approximately]464--400 Ma (Middle Ordovician to Early Devonian) for authigenic K-feldspar of two samples from the alteration profile widely developed over Precambrian rocks at the unconformity with Cambrian deposits. This dating was done on 42 to 48 mesh grains of K-feldspar by the laser incremental-heating [sup 40]Ar/[sup 39]Ar method. One sample, from west-central Wisconsin, is from an 8-mm-thick vein formed along a fracture in kaolinitic altered granite. Three grains nearest the fracture yielded plateau ages with a range of [approximately]9 Ma and an average of 430 Ma. Three grains distant from the fracture yielded a similar range of 10 Ma but with an average age of 397 Ma. Thus the grains grew over an extended period from at least [approximately]430 to 400 Ma. A K-Ar date of 411 Ma was obtained from a sample representing the entire thickness of the vein. The other sample, from the St. Francois Mts. of Missouri, is of diabase replaced by K-feldspar. Three grains yielded plateau ages ranging from [approximately]444 to 464 Ma. Oxygen-isotope values of authigenic K-feldspar from lower Paleozoic and uppermost Precambrian rocks range from +19.8 to +22.2[per thousand] and average 21.4[per thousand] (n = 11). These values are compatible with formation of the K-feldspar from similar fluids and comparable temperatures.

  10. Authigenic potassium feldspar: a tracer for the timing of palaeofluid flow in carbonate rocks, Northern Calcareous Alps, Austria

    USGS Publications Warehouse

    Spotl, C.; Kunk, M.J.; Ramseyer, K.; Longstaffe, F.J.

    1998-01-01

    This paper is included in the Special Publication entitled 'Dating and duration of fluid flow and fluid-rock interaction', edited by J. Parnell. Feldspar is a common authigenic constituent in Permian carbonate rocks which occur as tectonically isolated blocks within the evaporitic Haselgebirge melange in the Northern Calcareous Alps (NCA). Coexisting with pyrite, anhydrite, (saddle) dolomite, magnesite, fluorite and calcite, K-feldspar and minor albite record an event of regionally extensive interaction of hot brines with carbonate rocks. Detailed petrographic, crystallographic and geochemical studies reveal a variability in crystal size and shape, Al-Si ordering, elemental and stable isotopic compositions of the K-feldspar, which is only partially consistent with the traditional view of authigenic feldspar as a well-ordered, compositionally pure mineral. 40Ar-39Ar step- heating measurements of authigenic potassium feldspar from several localities yield two age populations, an older one of 145-154 Ma, and a younger one of c.90-97 Ma. Most age spectra reflect cooling through the argon retention temperature interval, which was rapid in some localities (as indicated by plateau ages) and slower in others. Rb-Sr isotope data are more difficult to interpret, because in many K-feldspar samples they are controlled largely by Sr-bearing inclusions. The Jurassic 40Ar-39Ar dates are interpreted as minimum ages of feldspar growth and hence imply that fluid-rock interaction is likely to be simultaneous with or to slightly predate melange formation. Deformation associated with the closure and subduction of the Meliata-Hallstatt ocean south of the NCA during the Upper Jurassic is regarded as the principal geodynamic driving force for both enhanced fluid circulation and melange formation. Some localities were reheated beyond the argon retention temperature for microcline during mid-Cretaceous nappe stacking of the NCA, thus obliterating the older signal.

  11. FTIR Analysis of Water in Pyroxene and Plagioclase in ALH 84001 and Nakhlites

    NASA Technical Reports Server (NTRS)

    Peslier, A. H.; Cintala, M. J.; Montes, R.; Cardenas, F.

    2016-01-01

    with crustal reservoirs or hydrothermal fluids. Here, nominally anhydrous minerals (pyroxene, olivine, plagioclase, or maskelynite) in orthopyroxenite ALH 84001 and selected nakhlites are analyzed for water and major elements, in order to determine 1) whether they contain any water; 2) if they do, what controls its distribution (crystallization, degassing, hydrothermal or impact processes); and 3) if any of these measurements can be used to infer the water contents of the parent magma and their mantle sources. A shock-reverberation experiment was also performed on terrestrial orthopyroxenes (opx) to simulate the heavily shocked conditions of ALH 84001 (> 31 GPa [17]).

  12. Wishstone to Watchtower: Alteration of Plagioclase-rich Rocks in Gusev Crater, Mars

    NASA Astrophysics Data System (ADS)

    Ruff, S. W.; Hamilton, V. E.

    2014-12-01

    The Mars Exploration Rover Spirit encountered a remarkable diversity of rocks during its traverse of the Columbia Hills in Gusev crater, manifested both as variations in primary mineralogy and in secondary alteration. The Wishstone and Watchtower Classes represent examples where the less altered (Wishstone) and more altered versions (Watchtower) were recognized as members of an alteration series identified by variations in geochemistry and Fe-bearing mineral phases [1-3]. Work by [1] demonstrated a geochemical relationship consistent with two-component mixing between a high Al2O3, TiO2, CaO, Na2O, P2O5 end-member and a second end-member enriched in MgO, Zn, S, Br, and Cl. The first end-member probably is Wishstone Class, with Watchtower Class intermediate between it and an unrecognized second end-member lithology [1]. New results using mirror-dust corrected spectra from Spirit's Miniature Thermal Emission Spectrometer [4] affirm the dominant plagioclase component in Wishstone and an amorphous component resembling basaltic glass in Watchtower identified previously [5]. But now we recognize a suite of rocks spanning the full range of alteration, including one dubbed Bruce that appears to be an alteration spectral end-member [4]. The spectra of some rocks with an intermediate level of alteration are well modeled as a simple two-component mixture of Wishstone and Bruce spectra. This is consistent with a style of alteration that progressively obscures spectral contributions of the host rock minerals and is inconsistent with a surface coating. The Bruce spectrum is poorly modeled by primary and secondary phases including phyllosilicates and amorphous silicates. This suggests a style of alteration not recognized in terrestrial settings. Based on the similarity of the Bruce spectrum to TES type 2, this style of alteration may be more widespread on Mars. The conditions that produced this alteration are poorly constrained, hence the relationship to habitability is unknown at

  13. [Influence of surface roughness on degree of polarization of biotite plagioclase gneiss varying with viewing angle].

    PubMed

    Xiang, Yun; Yan, Lei; Zhao, Yun-sheng; Gou, Zhi-yang; Chen, Wei

    2011-12-01

    Polarized reflectance is influenced by such factors as its physical and chemical properties, the viewing geometry composed of light incident zenith, viewing zenith and viewing azimuth relative to light incidence, surface roughness and texture, surface density, detection wavelengths, polarization phase angle and so on. In the present paper, the influence of surface roughness on the degree of polarization (DOP) of biotite plagioclase gneiss varying with viewing angle was inquired and analyzed quantitatively. The polarized spectra were measured by ASD FS3 spectrometer on the goniometer located in Northeast Normal University. When the incident zenith angle was fixed at 50 degrees, it was showed that on the rock surfaces with different roughness, in the specular reflection direction, the DOP spectrum within 350-2500 nm increased to the highest value first, and then began to decline varying with viewing zenith angle from 0 degree to 80 degrees. The characterized band (520 +/- 10) nm was picked out for further analysis. The correlation analysis between the peak DOP value of zenith and surface roughness showed that they are in a power function relationship, with the regression equation: y = 0.604x(-0.297), R2 = 0.985 4. The correlation model of the angle where the peak is in and the surface roughness is y = 3.4194x + 51.584, y < 90 degrees , R2 = 0.8177. With the detecting azimuth farther away from 180 degrees azimuth where the maximum DOP exists, the DOP lowers gradually and tends to 0. In the detection azimuth 180 dgrees , the correlation analysis between the peak values of DOP on the (520 =/- 10) nm band for five rocks and their surface roughness indicates a power function, with the regression equation being y = 0.5822x(-0.333), R2 = 0.9843. F tests of the above regression models indicate that the peak value and its corresponding viewing angle correlate much with surface roughness. The study provides a theoretical base for polarization remote sensing, and impels the

  14. Anomalous isotopes and trace element zoning in plagioclase peridotite xenoliths of Oahu (Hawaii): implications for the Hawaiian plume

    NASA Astrophysics Data System (ADS)

    Sen, Gautam; Yang, Huai-Jen; Ducea, Mihai

    2003-02-01

    Survival of plagioclase in the residual melting column during melting can have a significant impact on the melting process beneath a mid-oceanic ridge [Asimow et al., Phil. Trans. R. Soc. London Ser. A 355 (1997) 255-281]. Here we investigate the origin of plagioclase that occurs in some rare mantle xenoliths from Oahu, Hawaii. The xenoliths are harzburgitic with less than 2 modal% clinopyroxene and are characterized by strong foliation and porphyroclastic texture. Olivine and orthopyroxene are common porphyroclasts; and only one xenolith (77PAII-9) contains a single large clinopyroxene porphyroclast with thick exsolved orthopyroxene lamellae. The strongly foliated groundmass shows well-developed triple-point junctions and is dominantly composed of olivine (ol 85-90 opx 7-14 cpx <1-2 plag 3-5 spinel trace). Spinel grains are small and dispersed through the groundmass and show extreme variation in Cr/Al ratio within individual thin sections, indicating that they are out of equilibrium with the other phases in these xenoliths. A highly anorthitic plagioclase (An 92-96) occurs only in the groundmass and its modal abundance (˜3-5%) is too high relative to the abundance of clinopyroxene (commonly <1%) for it to be a residual phase, implying that plagioclase may have an exotic origin. The porphyroclasts show strong compositional zoning near the rims and appear to be relict phases (as are all the spinel grains) that had once equilibrated with melts within the stability field of spinel peridotite (pressure ˜1-3 GPa). Clinopyroxene neoblasts and the single porphyroclast in PAII-9 are all characterized by lithosphere-like strongly depleted light rare earth element (chondrite-normalized) patterns. The clinopyroxene porphyroclast in PAII-9 is zoned in Al, Eu, Cr, and Na. The porphyroclastic ortho- and clinopyroxenes give a homogenized (host+exsolution) temperature of 1300°C, which is inferred to be the temperature at which the porphyroclast cores equilibrated with a MORB

  15. CO2 sequestration in feldspar-rich sandstone: Coupled evolution of fluid chemistry, mineral reaction rates, and hydrogeochemical properties

    NASA Astrophysics Data System (ADS)

    Tutolo, Benjamin M.; Luhmann, Andrew J.; Kong, Xiang-Zhao; Saar, Martin O.; Seyfried, William E.

    2015-07-01

    To investigate CO2 Capture, Utilization, and Storage (CCUS) in sandstones, we performed three 150 °C flow-through experiments on K-feldspar-rich cores from the Eau Claire formation. By characterizing fluid and solid samples from these experiments using a suite of analytical techniques, we explored the coupled evolution of fluid chemistry, mineral reaction rates, and hydrogeochemical properties during CO2 sequestration in feldspar-rich sandstone. Overall, our results confirm predictions that the heightened acidity resulting from supercritical CO2 injection into feldspar-rich sandstone will dissolve primary feldspars and precipitate secondary aluminum minerals. A core through which CO2-rich deionized water was recycled for 52 days decreased in bulk permeability, exhibited generally low porosity associated with high surface area in post-experiment core sub-samples, and produced an Al hydroxide secondary mineral, such as boehmite. However, two samples subjected to ∼3 day single-pass experiments run with CO2-rich, 0.94 mol/kg NaCl brines decreased in bulk permeability, showed generally elevated porosity associated with elevated surface area in post-experiment core sub-samples, and produced a phase with kaolinite-like stoichiometry. CO2-induced metal mobilization during the experiments was relatively minor and likely related to Ca mineral dissolution. Based on the relatively rapid approach to equilibrium, the relatively slow near-equilibrium reaction rates, and the minor magnitudes of permeability changes in these experiments, we conclude that CCUS systems with projected lifetimes of several decades are geochemically feasible in the feldspar-rich sandstone end-member examined here. Additionally, the observation that K-feldspar dissolution rates calculated from our whole-rock experiments are in good agreement with literature parameterizations suggests that the latter can be utilized to model CCUS in K-feldspar-rich sandstone. Finally, by performing a number of reactive

  16. Authigenic K-NH{sub 4}-feldspar in sandstones: A fingerprint of the diagenesis of organic matter

    SciTech Connect

    Ramseyer, K.; Diamond, L.W.; Boles, J.R.

    1993-11-01

    In arkosic sandstones of the San Joaquin and Los Angeles Basins presently at temperatures between 35 C and 174 C, trace amounts of authigenic K-NH{sub 4}-feldspar are present as microfracture fillings and overgrowths on detrital K-feldspar. Microchemical analyses of this authigenic phase reveal up to 80 mole % buddingtonite. The largest ammonium concentrations are observed in a sandy interval of the Antelope shale (80 mole %) and in the Stevens Sands ({approx} 50 mole %) of the San Joaquin Basin. This latter unit was deposited as a turbidite in the organic-rich Fruitvale Shale, an equivalent of the Antelope Shale. The lowest ammonium contents (0-16 mole %) are present in the shallow-marine Vedder Sands and the marginal marine San Joaquin Formation in the same basin. Petrographic, {delta}{sup 18}O, {delta}{sup 13}C, and {sup 87}Sr/{sup 86}Sr analyses of a dolomite cement that postdates authigenic K-NH{sub 4}-feldspar indicate that the feldspar precipitated below 28 C in the zone of methanogenesis, from pore waters with the same Sr signature as sea water at the time of sedimentation. Authigenic K-NH{sub 4}-feldspar is thus an early-diagenetic phase that crystallized prior to oil migration, under anoxic conditions when organic matter releases ammonium. The source of ammonium is bacterial decay of organic matter in the sandstones themselves and/or in contemporaneous shales.

  17. Ion microprobe investigation of plagioclase and orthopyroxene from lunar Mg-suite norites: Implications for calculating parental melt REE concentrations and for assessing postcrystallization REE redistribution

    SciTech Connect

    Papike, J.J.; Fowler, G.W.; Shearer, C.K.; Layne, G.D.

    1996-10-01

    The lunar Mg-suite, which includes dunites, troctolites, and norites, makes up to 20-30% of the Moon`s crust down to a depth of {approximately}60 km. The remainder is largely anorthosite. This report focuses on norites (which consist mostly of orthopyroxene and plagioclase) because we have found that both phases are effective recorders of their parental melt compositions. In an earlier report, we analyzed orthopyroxene from twelve samples (three from Apollo 14, two from A-15, and seven from A-17) by orthopyroxene from twelve samples (three from Apollo 14, two from A-15, and seven from A-17) by SIMS for eight REE (La, Ce, Nd, Sm, Eu, Dy, Er, Yb). Inversion of these data to estimated melt compositions yielded extremely high REE concentrations similar to KREEP. In this study, we report SIMS REE data for plagioclase from these same twelve samples. The major objective of this study is to estimate parental REE concentrations from both orthopyroxene and plagioclase data to see if both data inversions produce concordant from both orthopyroxene and plagioclase data to see if both data inversions produce concordant melt compositions and thus better constrain the composition of melts parental to Mg-suite norites. The estimated REE concentrations from both phases show some evidence of slight postcrystallization REE redistribution. Comparison of the observed ratio of REE for pyroxene/plagioclase to the ratio of the Ds for pyroxene/plagioclase is consistent with REE redistribution which involves LREE diffusing from pyroxene into plagioclase and HREE diffusing from plagioclase into pyroxene. However, apparently these postcrystallization exchanges have not seriously affected our ability to estimate melt REE concentrations. 34 refs., 7 figs., 5 tabs.

  18. Water content in arc basaltic magma in the Northeast Japan and Izu arcs: an estimate from Ca/Na partitioning between plagioclase and melt

    NASA Astrophysics Data System (ADS)

    Ushioda, Masashi; Takahashi, Eiichi; Hamada, Morihisa; Suzuki, Toshihiro

    2014-12-01

    The variation in water content of arc basaltic magmas in the Northeast Japan arc and the Izu arc was estimated using a simple plagioclase phenocryst hygrometer. In order to construct a plagioclase phenocryst hygrometer optimized for arc basalt magmas, we have conducted high-pressure melting experiments of relatively primitive basalt from the Miyakejima volcano, a frontal-arc volcano in the Izu arc. As a result of the experiments, we found that the Ca/Na partition coefficient between plagioclase and hydrous basaltic melt increases linearly with an increase in H2O content in the melts. We then selected from literature geochemical data sets of relatively primitive basaltic rocks with no evidence of magma mixing and the most frequent Ca-rich plagioclase phenocrysts from 15 basaltic arc volcanoes including both frontal-arc and rear-arc volcanoes. In the 15 volcanoes studied, plagioclase phenocrysts of high anorthite content (An > 90) were commonly observed, whereas plagioclase phenocrysts in rear arc volcanoes usually had a lower anorthite content (90 > An > 80). In all volcanoes studied, the estimated H2O content of basaltic magma was at least 3 wt.% H2O or higher. The magmas of volcanoes located on the volcanic front have about 5 wt.% H2O in magma whereas those from the rear-arc side are slightly lower in H2O content.

  19. Water content in arc basaltic magma in the Northeast Japan and Izu arcs: an estimate from Ca/Na partitioning between plagioclase and melt

    NASA Astrophysics Data System (ADS)

    Ushioda, M.; Takahashi, E.; Hamada, M.; Suzuki, T.

    2015-12-01

    The variation in water content of arc basaltic magmas in the Northeast Japan arc and the Izu arc was estimatedusing a simple plagioclase phenocryst hygrometer. In order to construct a plagioclase phenocryst hygrometeroptimized for arc basalt magmas, we have conducted hydrous melting experiments of relatively primitive basaltfrom the Miyakejima volcano, a frontal-arc volcano in the Izu arc. As a result of the experiments, we found that theCa/Na partition coefficient between plagioclase and hydrous basaltic melt increases linearly with an increase in H2Ocontent in the melts. We then compiled published geochemical data sets of relatively primitive basaltic rocks with no evidence of magma mixing and the most frequent Ca-rich plagioclase phenocrysts from 15 basaltic arc volcanoesincluding both frontal-arc and rear-arc volcanoes. In the 15 volcanoes studied, plagioclase phenocrysts of high anorthitecontent (An > 90) were commonly observed, whereas plagioclase phenocrysts in rear arc volcanoes usually had a loweranorthite content (90 > An > 80). In all volcanoes studied, the estimated H2O content of basaltic magma was at least3 wt.% H2O or higher. The magmas of volcanoes located on the volcanic front have about 5 wt.% H2O in magmawhereas those from the rear-arc side are slightly lower in H2O content.

  20. The importance of plagioclase in the reflectance spectra of Fe, Mg mixtures: a better understanding of spectra from Lunar and Hermean terrains.

    NASA Astrophysics Data System (ADS)

    Serventi, G.; Sgavetti, M.; Carli, C.; Pompilio, L.

    2012-04-01

    Spectra obtained on Lunar highland and on Mercury show low contrast features. We suggest the interference of adjacent absorptions bands due to different minerals as a possible cause of low contrast spectra. While the combined effects of Fe2+ absorptions in various clinopyroxene, orthopyroxene and olivine mixtures have been widely studied, the spectroscopic effects of plagioclase have been considered only for <0,26 wt% FeO-bearing compositions, even if plagioclase is considered an important constituent of Lunar and Hermean terrains. Here we consider mixtures composed by various abundances of multimineral grains and plagioclase, separated from cumulate rocks of a layered intrusion belonging to the anorthosite kindred. Three different Fe, Mg multimineral compositions have been considered. The first is olivine-free and consists of clinopyroxene En45-Wo46 (43.9%) and orthopyroxene En77 (56.1%). The second one is olivine-poor and includes orthopyroxene En86 (70%) and olivine Fo87 (30%). The third one, olivine-rich, is composed by orthopyroxene En82 (28.2%), clinopyroxene En45-Wo46 (3.4%), olivine Fo84 (68.4%). Two distinct plagioclase compositions, having FeO wt.% concentration of 0.36 (medium-iron), and 0.5 (rich-iron) were systematically mixed to each starting assemblage. The amount of plagioclase in the mixtures ranges between 30% and 90%. Mixtures with grain sizes of 63-125 μm and 125-250 μm were prepared. Bidirectional reflectance spectra (i=30°, e=0° angle phase) on these mixtures were acquired at the SLAB (Spectroscopy Laboratory, Iasf-INAF, Roma) in the VIS-NIR range (0.3-2.5 µm). Preliminary results show that increasing plagioclase content produces higher albedo and lower spectral contrast. In olivine-free mixtures, plagioclase produces a flattening in the 1.2 µm region at about 70% of medium-iron plagioclase and 50% of iron-rich plagioclase; for higher content of plagioclase a clear absorption band appears. In olivine-poor mixtures, the presence of

  1. Characterization of Quartz and Feldspar Deformation in the Mid-crust: Insights from the Cordillera Blanca Shear Zone, Peru

    NASA Astrophysics Data System (ADS)

    Hughes, C. A.; Jessup, M. J.; Shaw, C. A.

    2014-12-01

    Deformation mechanisms within shear zones from various crustal levels must be characterized to develop accurate models of lithospheric rheology. The Cordillera Blanca Shear Zone (CBSZ) in the central Peruvian Andes records changes in temperature, microstructures, and deformation mechanisms that occurred during exhumation through the brittle-ductile-transition during normal-sense slip over the last ~5 m.y. The 100-500-m-thick mylonitic shear zone occupies the footwall of a 200-km-long normal detachment fault, marking the western boundary of the 8 Ma, leucogranodiorite Cordillera Blanca Batholith. Though local variations do occur, including recrystallized quartz veins and local, decimeter- to meter- scale shear zones, the CBSZ follows a general trend of increasing strain towards the detachment. Structurally lowest positions are weakly deformed and transition to protomylonite, mylonite, and ultramylonite at higher positions, truncating at a cataclasite nearest the detachment. We characterize strain using EBSD analyses of quartz lattice preferred orientations and deformation temperatures using quartz and feldspar textures and two-feldspar thermometry of asymmetric strain-induced myrmekite. At the deepest structural positions, feldspar grains record a complex history characterized by bulging recrystallization, myrmekite formation, and brittle fracture, while quartz exhibits dominant grain-boundary migration recrystallization (T> 500 °C) and prism slip. Intermediate samples exhibit more prevalent strain-induced myrmekite, brittle fracture in feldspar, and reaction-associated recrystallization of K-feldspar to mica; quartz records mainly subgrain-rotation recrystallization (400-500 °C) and dominant prism slip with a rhomb component. Shallower positions preserve fewer, smaller, and more rounded feldspar porphyroclasts with no myrmekite, and dominant bulging recrystallization (280-400 °C) in quartz that records prism , rhomb , and some basal slip.

  2. DIET of alkali atoms from mineral surfaces

    NASA Astrophysics Data System (ADS)

    Yakshinskiy, B. V.; Madey, T. E.

    2003-03-01

    To investigate mechanisms for the origin of alkalis in the atmosphere of the Moon, we are studying the electron- and photon-stimulated desorption (ESD and PSD) of K atoms from model mineral surfaces (SiO 2 films), and ESD and PSD of Na atoms from a lunar basalt sample. X-ray photoelectron spectroscopy demonstrates the existence of traces of Na in the lunar sample. To obtain an increased signal for detailed measurements of desorption parameters (appearance thresholds, yields), a fractional monolayer of Na is deposited onto the lunar sample surface. An alkali atom detector based on surface ionization and a time-of-flight technique are used for DIET measurements, together with a pulsed electron gun, and a mechanically chopped and filtered mercury arc light source. We find that bombardment of the alkali covered surfaces by UV photons or by electrons with energies E>4 eV causes desorption of "hot" alkali atoms. The results are consistent with the model based on charge transfer from the substrate to adsorbate which was developed to explain our previous measurements of sodium desorption from a silica surface and desorption of K atoms from water ice. The data support the suggestion that PSD by UV solar photons is a dominant source process for alkalis in the tenuous lunar atmosphere.

  3. Constraints on the accretion of the gabbroic lower oceanic crust from plagioclase lattice preferred orientation in the Samail ophiolite

    NASA Astrophysics Data System (ADS)

    VanTongeren, J. A.; Hirth, G.; Kelemen, P. B.

    2015-12-01

    The debate over the processes of igneous accretion of gabbroic lower crust at submarine spreading centers is centered on two end-member hypotheses: Gabbro Glaciers and Sheeted Sills. In order to determine which of these two hypotheses is most applicable to a well-studied lower crustal section, we present newly published data (VanTongeren et al., 2015 EPSL v. 427, p. 249-261) on plagioclase lattice preferred orientations (LPO) in the Wadi Khafifah section of the Samail ophiolite, Oman. Based on our results we provide five critical observations that any model for the accretion of the lower oceanic crust must satisfy: (1) There is a distinctive change in the orientation of the outcrop-scale layering from near-vertical to sub-horizontal that is also reflected in the plagioclase fabrics in the uppermost ~1000-1500 m of the gabbroic crust; (2) The distinction between the upper gabbros and lower gabbros is not a geochemical boundary. Rather, the change in outcrop-scale orientation from near-vertical to sub-horizontal occurs stratigraphically lower in the crust than a change in whole-rock geochemistry; (3) There is no systematic difference in plagioclase fabric strength in any crystallographic axis between the upper gabbros and the lower gabbros; (4) Beneath the abrupt transition from sub-vertical to sub-horizontal fabric, there is no systematic change in the geographic orientation of the plagioclase fabric, or in the development of a dominant lineation direction within the upper gabbros or the lower gabbros; (5) In the lower gabbros, the obliquity between the (010) and the modal layering remains approximately constant and indicates a consistent top to the right sense of shear throughout the stratigraphy. Our observations are most consistent with the Sheeted Sills hypothesis, in which the majority of lower crustal gabbros are crystallized in situ and fabrics are dominated by compaction and localized extension rather than by systematically increasing shear strain with

  4. Effect of Plagioclase Crystallization on Liquid and Magma Viscosity in the An-Di-Fo-Q System

    NASA Astrophysics Data System (ADS)

    Getson, J. M.; Whittington, A.

    2006-05-01

    In this study we compare the chemical effect of changing composition on residual liquid viscosity and the physical effect of entrained crystals on magma viscosity during plagioclase crystallization. Seventeen CMAS glasses based on dacitic and basaltic bulk compositions were synthesized. Eight are contained in the An-Di- Fo system lying approximately on the An-Di90Fo10 pseudobinary and running through the 1 atm eutectic; nine form two separate series in the An-Fo-Q system. The first lies on the An-En binary between An and the An-En cotectic; the second joins anorthite and the An-En-Q eutectic. Liquid viscosities were measured in the range from 101 to 104 and 108 to 1012 Pa.s using concentric cylinder and parallel plate viscometry. Liquidus viscosities were interpolated using TVF equations fitted to both low and high temperature datasets. Viscosity varies smoothly with liquid composition. Within the anorthite field of the An-En binary, a starting liquid of molar composition An50Fo25Q25 has a viscosity of 101.5 Pa.s at the liquidus temperature of 1400°C. Progressive crystallization generates liquid of An34Fo33Q33 on the An-En cotectic, with a viscosity of 101.4 Pa.s at its liquidus temperature of 1300°C. Therefore, plagioclase fractionation can lead to constant or decreasing liquid viscosities even during cooling due to changing liquid composition. Magma viscosity depends on both the liquid viscosity and the physical effect of crystals. For the same example, assuming the 37% volume fraction of plagioclase crystals are fully retained, the calculated magma viscosity would be 102.45 Pa.s. These results confirm that magma viscosities increase with crystallization, but demonstrate that residual liquid composition must be accounted for. Tracking viscosity during progressive cooling and plagioclase crystallization suggests that magma viscosity will initially decrease, as changing liquid composition outweighs decreasing temperature and increasing crystal content. At higher

  5. Subsurface damage induced in dental resurfacing of a feldspar porcelain with coarse diamond burs.

    PubMed

    Song, Xiao-Fei; Yin, Ling

    2009-02-01

    The primary cause for early failure of ceramic restorations is surface and subsurface damage induced in adjustment and resurfacing using dental handpieces/burs. This paper reports finite element analysis (FEA) modelling of dental resurfacing to predict the degrees of subsurface damage, in combination with experimental measurement using scanning electron microscopy (SEM). The FEA predictions of subsurface damage induced in a feldspar porcelain with coarse diamond burs were in agreement with the SEM experimental measurement. These findings provide dental clinicians a quantitative description of the response of dental resurfacing-induced subsurface damage. The implication of the results for non-destructive evaluation of subsurface damage by FEA modelling will be practically meaningful to clinical dental restorations for high-quality ceramic restorations. PMID:19144338

  6. Laboratory measurements of upwelled radiance and reflectance spectra of Calvert, Ball, Jordan, and Feldspar soil sediments

    NASA Technical Reports Server (NTRS)

    Whitlock, C. H.; Usry, J. W.; Witte, W. G.; Gurganus, E. A.

    1977-01-01

    An effort to investigate the potential of remote sensing for monitoring nonpoint source pollution was conducted. Spectral reflectance characteristics for four types of soil sediments were measured for mixture concentrations between 4 and 173 ppm. For measurements at a spectral resolution of 32 mm, the spectral reflectances of Calvert, Ball, Jordan, and Feldspar soil sediments were distinctly different over the wavelength range from 400 to 980 nm at each concentration tested. At high concentrations, spectral differences between the various sediments could be detected by measurements with a spectral resolution of 160 nm. At a low concentration, only small differences were observed between the various sediments when measurements were made with 160 nm spectral resolution. Radiance levels generally varied in a nonlinear manner with sediment concentration; linearity occurred in special cases, depending on sediment type, concentration range, and wavelength.

  7. Refractories for high-alkali environments

    SciTech Connect

    Rau, A.W.; Cloer, F.

    1996-01-01

    There are two reliable and cost-effective tests for evaluating refractory materials. They are used to determine which refractory products allow greater variance in fuel type with respect to alkali environment for coal-fired applications. Preselection of a particular refractory is important because of down-time cost for premature failure. One test is a variation of the standard alkali cup test. The second involves reacting test specimens with the contaminant, followed by physical properties testing to determine degree of degradation and properties affected. The alkali cup test rates products using a relative numerical scale based upon visual appearance. This test indicates the presence and relative degree of chemical attack to the refractory. The physical properties test determines the specific properties affected by the given contaminant.

  8. Alkali metal vapors - Laser spectroscopy and applications

    NASA Technical Reports Server (NTRS)

    Stwalley, W. C.; Koch, M. E.

    1980-01-01

    The paper examines the rapidly expanding use of lasers for spectroscopic studies of alkali metal vapors. Since the alkali metals (lithium, sodium, potassium, rubidium and cesium) are theoretically simple ('visible hydrogen'), readily ionized, and strongly interacting with laser light, they represent ideal systems for quantitative understanding of microscopic interconversion mechanisms between photon (e.g., solar or laser), chemical, electrical and thermal energy. The possible implications of such understanding for a wide variety of practical applications (sodium lamps, thermionic converters, magnetohydrodynamic devices, new lasers, 'lithium waterfall' inertial confinement fusion reactors, etc.) are also discussed.

  9. An exsolution silica-pump model for the origin of myrmekite

    USGS Publications Warehouse

    Castle, R.O.; Lindsley, D.H.

    1993-01-01

    Myrmekite, as defined here, is the microscopic intergrowth between vermicular quartz and modestly anorthitic plagioclase (calcic albite-oligoclase), intimately associated with potassium feldspar in plutonic rocks of granitic composition. Hypotheses previously invoked in explanation of myrmekite include: (1) direct crystallization; (2) replacement; (3) exsolution. The occurrence of myrmekite in paragneisses and its absence in rocks devold of discrete grains of potassium feldspar challenge those hypotheses based on direct crystallization or replacement. However, several lines of evidence indicate that myrmekite may in fact originate in response to kinetic effects associated with the exsolution of calcic alkali feldspar into discrete potassium feldspar and plagioclase phases. Exsolution of potassium feldspar system projected from [AlSi2O8] involves the exchange CaAlK-1Si-1, in which the AlSi-1 tetrahedral couple is resistant to intracrystalline diffusion. By contrast, diffusion of octahedral K proceeds relatively easily where it remains uncoupled to the tetrahedral exchange. We suggest here that where the ternary feldspar system is open to excess silica, the exchange reaction that produces potassium feldspar in the ternary plane is aided by the net-transfer reaction K+Si=Orthoclase, leaving behind indigenous Si that reports as modal quartz in the evolving plagioclase as the CaAl component is concomitantly incorporated in this same phase. Thus silica is "pumped" into the reaction volume from a "silica reservoir", a process that enhances redistribution of both Si and Al through the exsolving ternary feldspar. ?? 1993 Springer-Verlag.

  10. An exsolution silica-pump model for the origin of myrmekite

    NASA Astrophysics Data System (ADS)

    Castle, Robert O.; Lindsley, Donald H.

    1993-03-01

    Myrmekite, as defined here, is the microscopic intergrowth between vermicular quartz and modestly anorthitic plagioclase (calcic albite-oligoclase), intimately associated with potassium feldspar in plutonic rocks of granitic composition. Hypotheses previously invoked in explanation of myrmekite include: (1) direct crystallization; (2) replacement; (3) exsolution. The occurrence of myrmekite in paragneisses and its absence in rocks devold of discrete grains of potassium feldspar challenge those hypotheses based on direct crystallization or replacement. However, several lines of evidence indicate that myrmekite may in fact originate in response to kinetic effects associated with the exsolution of calcic alkali feldspar into discrete potassium feldspar and plagioclase phases. Exsolution of potassium feldspar system projected from [AlSi2O8] involves the exchange CaAlK-1Si-1, in which the AlSi-1 tetrahedral couple is resistant to intracrystalline diffusion. By contrast, diffusion of octahedral K proceeds relatively easily where it remains uncoupled to the tetrahedral exchange. We suggest here that where the ternary feldspar system is open to excess silica, the exchange reaction that produces potassium feldspar in the ternary plane is aided by the net-transfer reaction K+Si=Orthoclase, leaving behind indigenous Si that reports as modal quartz in the evolving plagioclase as the CaAl component is concomitantly incorporated in this same phase. Thus silica is “pumped” into the reaction volume from a “silica reservoir”, a process that enhances redistribution of both Si and Al through the exsolving ternary feldspar.

  11. Experimental determination of plagioclase dissolution rates as a function of its composition and pH at 22 °C

    NASA Astrophysics Data System (ADS)

    Gudbrandsson, Snorri; Wolff-Boenisch, Domenik; Gislason, Sigurdur R.; Oelkers, Eric H.

    2014-08-01

    The steady-state, far-from-equilibrium dissolution rates of nine distinct plagioclases ranging in composition from An2 to An89 were measured in mixed flow reactors at 22 ± 2 °C and pH from 2 to 11. The dissolution rates of all plagioclases based on silica release show a common U-shaped behaviour as a function of pH, where rates decrease with increasing pH at acid condition but rise with increasing pH at alkaline conditions. Consistent with literature findings, constant pH plagioclase dissolution rates increase with increasing anorthite content at acidic conditions; measured anorthite dissolution rates are ∼2.5 orders of magnitude faster than those of albite at pH ∼2. Perhaps more significantly, rates are independent of plagioclase composition at alkaline conditions. Interpretation and data fitting suggests that plagioclase dissolution rates are consistent with their control by the detachment of Si-rich activated complexes formed by the removal of Al from the mineral framework. Taking account of this mechanism and transition state theory yields equations describing plagioclase dissolution rates (r+) as a function of both the mineral and aqueous fluid compositions found in natural Earth surface systems. For pH ⩾ 6 rates are consistent with Log(r+/(mol/cm/s))=0.35Log(aH3/aAl)-11.53 and for pH < 6 rates are consistent with Log(r+/(mol/cm/s))=nacidLog(aH3/aAl)+0.033An%-14.77 where An% represents the percent anorthite in the plagioclase solid solution, ai corresponds to the activity of the ith aqueous species, and nacid is given by nacid=0.004An%+0.05 .

  12. Recovery of alkali metal constituents from catalytic coal conversion residues

    DOEpatents

    Soung, W.Y.

    In a coal gasification operation (32) or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles by contacting them with water or an aqueous solution to remove water-soluble alkali metal constituents and produce an aqueous solution enriched in said constituents. The aqueous solution thus produced is then contacted with carbon dioxide to precipitate silicon constituents, the pH of the resultant solution is increased, preferably to a value in the range between about 12.5 and about 15.0, and the solution of increased pH is evaporated to increase the alkali metal concentration. The concentrated aqueous solution is then recycled to the conversion process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst.

  13. Salts of alkali metal anions and process of preparing same

    DOEpatents

    Dye, James L.; Ceraso, Joseph M.; Tehan, Frederick J.; Lok, Mei Tak

    1978-01-01

    Compounds of alkali metal anion salts of alkali metal cations in bicyclic polyoxadiamines are disclosed. The salts are prepared by contacting an excess of alkali metal with an alkali metal dissolving solution consisting of a bicyclic polyoxadiamine in a suitable solvent, and recovered by precipitation. The salts have a gold-color crystalline appearance and are stable in a vacuum at -10.degree. C. and below.

  14. 40 CFR 721.1878 - Alkali metal alkyl borohydride (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Alkali metal alkyl borohydride... Specific Chemical Substances § 721.1878 Alkali metal alkyl borohydride (generic). (a) Chemical substance... alkali metal alkyl borohydride (PMN P-00-1089) is subject to reporting under this section for...

  15. 40 CFR 721.1878 - Alkali metal alkyl borohydride (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alkali metal alkyl borohydride... Specific Chemical Substances § 721.1878 Alkali metal alkyl borohydride (generic). (a) Chemical substance... alkali metal alkyl borohydride (PMN P-00-1089) is subject to reporting under this section for...

  16. 40 CFR 721.1878 - Alkali metal alkyl borohydride (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkali metal alkyl borohydride... Specific Chemical Substances § 721.1878 Alkali metal alkyl borohydride (generic). (a) Chemical substance... alkali metal alkyl borohydride (PMN P-00-1089) is subject to reporting under this section for...

  17. 40 CFR 721.1878 - Alkali metal alkyl borohydride (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alkali metal alkyl borohydride... Specific Chemical Substances § 721.1878 Alkali metal alkyl borohydride (generic). (a) Chemical substance... alkali metal alkyl borohydride (PMN P-00-1089) is subject to reporting under this section for...

  18. 40 CFR 721.1878 - Alkali metal alkyl borohydride (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Alkali metal alkyl borohydride... Specific Chemical Substances § 721.1878 Alkali metal alkyl borohydride (generic). (a) Chemical substance... alkali metal alkyl borohydride (PMN P-00-1089) is subject to reporting under this section for...

  19. 40 CFR 721.4660 - Alcohol, alkali metal salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alcohol, alkali metal salt. 721.4660... Substances § 721.4660 Alcohol, alkali metal salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance generically identified as alcohol, alkali metal salt (PMN P-91-151)...

  20. 40 CFR 721.4660 - Alcohol, alkali metal salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alcohol, alkali metal salt. 721.4660... Substances § 721.4660 Alcohol, alkali metal salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance generically identified as alcohol, alkali metal salt (PMN P-91-151)...

  1. 40 CFR 721.4660 - Alcohol, alkali metal salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alcohol, alkali metal salt. 721.4660... Substances § 721.4660 Alcohol, alkali metal salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance generically identified as alcohol, alkali metal salt (PMN P-91-151)...

  2. 40 CFR 721.4660 - Alcohol, alkali metal salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Alcohol, alkali metal salt. 721.4660... Substances § 721.4660 Alcohol, alkali metal salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance generically identified as alcohol, alkali metal salt (PMN P-91-151)...

  3. 40 CFR 721.4660 - Alcohol, alkali metal salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Alcohol, alkali metal salt. 721.4660... Substances § 721.4660 Alcohol, alkali metal salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance generically identified as alcohol, alkali metal salt (PMN P-91-151)...

  4. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  5. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  6. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  7. 40 CFR 721.8900 - Substituted halogenated pyridinol, alkali salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., alkali salt. 721.8900 Section 721.8900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.8900 Substituted halogenated pyridinol, alkali salt. (a) Chemical... as substituted halogenated pyridinols, alkali salts (PMNs P-88-1271 and P-88-1272) are subject...

  8. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  9. 40 CFR 721.5278 - Substituted naphthalenesulfonic acid, alkali salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., alkali salt. 721.5278 Section 721.5278 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.5278 Substituted naphthalenesulfonic acid, alkali salt. (a) Chemical... as a substituted naphthalenesulfonic acid, alkali salt (PMN P-95-85) is subject to reporting...

  10. 40 CFR 721.8900 - Substituted halogenated pyridinol, alkali salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., alkali salt. 721.8900 Section 721.8900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.8900 Substituted halogenated pyridinol, alkali salt. (a) Chemical... as substituted halogenated pyridinols, alkali salts (PMNs P-88-1271 and P-88-1272) are subject...

  11. 40 CFR 721.8900 - Substituted halogenated pyridinol, alkali salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., alkali salt. 721.8900 Section 721.8900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.8900 Substituted halogenated pyridinol, alkali salt. (a) Chemical... as substituted halogenated pyridinols, alkali salts (PMNs P-88-1271 and P-88-1272) are subject...

  12. 40 CFR 721.8900 - Substituted halogenated pyridinol, alkali salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., alkali salt. 721.8900 Section 721.8900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.8900 Substituted halogenated pyridinol, alkali salt. (a) Chemical... as substituted halogenated pyridinols, alkali salts (PMNs P-88-1271 and P-88-1272) are subject...

  13. Alkali resistant optical coatings for alkali lasers and methods of production thereof

    SciTech Connect

    Soules, Thomas F; Beach, Raymond J; Mitchell, Scott C

    2014-11-18

    In one embodiment, a multilayer dielectric coating for use in an alkali laser includes two or more alternating layers of high and low refractive index materials, wherein an innermost layer includes a thicker, >500 nm, and dense, >97% of theoretical, layer of at least one of: alumina, zirconia, and hafnia for protecting subsequent layers of the two or more alternating layers of high and low index dielectric materials from alkali attack. In another embodiment, a method for forming an alkali resistant coating includes forming a first oxide material above a substrate and forming a second oxide material above the first oxide material to form a multilayer dielectric coating, wherein the second oxide material is on a side of the multilayer dielectric coating for contacting an alkali.

  14. Computational studies of solid-state alkali conduction in rechargeable alkali-ion batteries

    DOE PAGES

    Deng, Zhi; Mo, Yifei; Ong, Shyue Ping

    2016-03-25

    The facile conduction of alkali ions in a crystal host is of crucial importance in rechargeable alkali-ion batteries, the dominant form of energy storage today. In this review, we provide a comprehensive survey of computational approaches to study solid-state alkali diffusion. We demonstrate how these methods have provided useful insights into the design of materials that form the main components of a rechargeable alkali-ion battery, namely the electrodes, superionic conductor solid electrolytes and interfaces. We will also provide a perspective on future challenges and directions. Here, the scope of this review includes the monovalent lithium- and sodium-ion chemistries that aremore » currently of the most commercial interest.« less

  15. Ingestion of caustic alkali farm products.

    PubMed

    Neidich, G

    1993-01-01

    Since the Poison Prevention Packaging Act took effect, the number of ingestions of caustic alkali from household products has been significantly reduced. Commercial caustic alkalis used on farms, however, were not included in this legislation. Fourteen children over a 5 year period were seen after ingestion of commercial caustic alkalis used on farms. Seven of the children had ingested liquid pipeline cleaners and seven had ingested solid agents used for a variety of reasons. Six of seven children ingesting liquid agents did so from nonoriginal containers into which the caustic had been transferred for convenience. All seven children ingesting solid agents did so from the original container. Eight of the 14 children were found to have second-degree or worse esophageal involvement. Both solid and liquid caustic agents used commercially on farms can cause significant morbidity. Development of a child-resistant container for daily transfer of liquid pipeline agents could be helpful in preventing injuries from liquid pipeline cleaners. Pediatric gastroenterologists as well as primary care physicians in rural areas should be familiar with this type of injury and should take an active role in instructing parents of children living on farms to prevent such injuries. Extension of the Poison Prevention Packaging Act to caustic alkalis used on farms needs to be considered. PMID:8433244

  16. Terahertz radiation in alkali vapor plasmas

    SciTech Connect

    Sun, Xuan; Zhang, X.-C.

    2014-05-12

    By taking advantage of low ionization potentials of alkali atoms, we demonstrate terahertz wave generation from cesium and rubidium vapor plasmas with an amplitude nearly one order of magnitude larger than that from nitrogen gas at low pressure (0.02–0.5 Torr). The observed phenomena are explained by the numerical modeling based upon electron tunneling ionization.

  17. Ingestion of caustic alkali farm products.

    PubMed

    Neidich, G

    1993-01-01

    Since the Poison Prevention Packaging Act took effect, the number of ingestions of caustic alkali from household products has been significantly reduced. Commercial caustic alkalis used on farms, however, were not included in this legislation. Fourteen children over a 5 year period were seen after ingestion of commercial caustic alkalis used on farms. Seven of the children had ingested liquid pipeline cleaners and seven had ingested solid agents used for a variety of reasons. Six of seven children ingesting liquid agents did so from nonoriginal containers into which the caustic had been transferred for convenience. All seven children ingesting solid agents did so from the original container. Eight of the 14 children were found to have second-degree or worse esophageal involvement. Both solid and liquid caustic agents used commercially on farms can cause significant morbidity. Development of a child-resistant container for daily transfer of liquid pipeline agents could be helpful in preventing injuries from liquid pipeline cleaners. Pediatric gastroenterologists as well as primary care physicians in rural areas should be familiar with this type of injury and should take an active role in instructing parents of children living on farms to prevent such injuries. Extension of the Poison Prevention Packaging Act to caustic alkalis used on farms needs to be considered.

  18. The Additive Coloration of Alkali Halides

    ERIC Educational Resources Information Center

    Jirgal, G. H.; and others

    1969-01-01

    Describes the construction and use of an inexpensive, vacuum furnace designed to produce F-centers in alkali halide crystals by additive coloration. The method described avoids corrosion or contamination during the coloration process. Examination of the resultant crystals is discussed and several experiments using additively colored crystals are…

  19. Cohesive Energy of the Alkali Metals.

    ERIC Educational Resources Information Center

    Poole, R. T.

    1980-01-01

    Describes a method, considered appropriate for presentation to undergraduate students in materials science and related courses, for the calculation of cohesive energies of the alkali metals. Uses a description based on the free electron model and gives results to within 0.1 eV of the experimental values. (Author/GS)

  20. Contact freezing induced by biological (Snomax) and mineral dust (K-feldspar) particles

    NASA Astrophysics Data System (ADS)

    Hoffmann, N.; Schäfer, M.; Duft, D.; Kiselev, A. A.; Leisner, T.

    2013-12-01

    The contact freezing of supercooled cloud droplets is one of the potentially important and the least investigated heterogeneous mechanism of ice formation in tropospheric clouds [1]. On the time scales of cloud lifetime the freezing of supercooled water droplets via contact mechanism may occur at higher temperature compared to the same IN immersed in the droplet. In our experiment we study single water droplets freely levitated in an Electrodynamic Balance [2]. We have shown previously that the rate of freezing at given temperature is governed only by the rate of droplet -particle collision and by the properties of the contact ice nuclei [2, 3]. Recently, we have extended our experiments to feldspar, being the most abundant component of the atmospheric mineral dust particles, and Snomax, as a proxy for atmospheric biological Ice Nuclei (IN). In this contribution we show that both IN exhibits the same temperature, size and material dependency observed previously in immersion mode [4, 5]. Based on these results, we limit the number of mechanisms that could be responsible for the enhancement of contact nucleation of ice in supercooled water. [1] - Ladino, L. A., Stetzer, O., and Lohmann, U.: Contact freezing: a review, Atmos. Chem. Phys. Discuss., 13, 7811-7869, doi:10.5194/acpd-13-7811-2013, 2013. [2] - Hoffmann, N., Kiselev, A., Rzesanke, D., Duft, D., and Leisner, T.: Experimental quantification of contact freezing in an electrodynamic balance, Atmos. Meas. Tech. Discuss., 6, 3407-3437, doi:10.5194/amtd-6-3407-2013, 2013. [3] - Hoffmann, N., Duft, D., Kiselev, A., and Leisner, T.: Contact freezing efficiency of mineral dust aerosols studied in an electrodynamic balance: quantitative size and temperature dependence for illite particles, Faraday Discuss., doi: 10.1039/C3FD00033H, 2013. [4] - Atkinson, James D., Murray, Benjamin J., Woodhouse, Matthew T., Whale, Thomas F., Baustian, Kelly J., Carslaw, Kenneth S., Dobbie, Steven, O'Sullivan, Daniel, and Malkin, Tamsin

  1. Experimental quantification of P-T conditions of mantle refertilisation at shallow depth under spreading ridges and formation of plagioclase + spinel lherzolite

    NASA Astrophysics Data System (ADS)

    Chalot-Prat, Françoise; Falloon, Trevor J.; Green, David H.

    2014-05-01

    We studied the first-order melting process of differentiation in the Earth, and the major process of rejuvenation of the upper mantle after melting related to plate spreading (Chalot-Prat et al, 2010; 2013). We conducted experiments at High Pressure (0.75 and 0.5 GPa) and High Temperature (1260-1100°C) to obtain magma compositions in equilibrium with the mineral assemblages of a plagioclase + spinel lherzolite. These PT conditions prevail at 17-30km below axial oceanic spreading ridges. We used a "trial and error" approach in a system involving nine elements (Cr-Na-Fe-Ca-Mg-Al-Si-Ti-Ni). This approaches as closely as possible a natural mantle composition, Cr being a key element in the system. Our objectives were : • to determine experimentally the compositions of melts in equilibrium with plagioclase + spinel lherzolite, with emphasis on the role of plagioclase composition in controlling melt compositions; • to test the hypothesis that MORB are produced at shallow depth (17-30kms) • to quantify liquid- and mantle residue compositional paths at decreasing T and low P to understand magma differentiation by "percolation-reaction" at shallow depth in the mantle; • to compare experimental mantle mineral compositions to those of re-fertilised oceanic mantle lithosphere outcropping at the axis of oceanic spreading ridges, enabling quantification of the pressure (i.e. depth) and temperature of the re-fertilisation process that leads to formation of plagioclase and indicates the minimum thickness of the lithosphere at ridge axes. In the normative basalt tetrahedron, liquids plot on two parallel cotectic lines from silica-oversaturated (basaltic andesite at 0.75 GPa or andesite at 0.5 GPa) at the calcic end to silica-undersaturated compositions (trachyte) at the sodic end. The lower the pressure, the greater the silica oversaturation. Besides the plagioclase solid solution has a dominant role in determining the solidus temperature of plagioclase + spinel lherzolites

  2. Calcic amphibole thermobarometry in metamorphic and igneous rocks: New calibrations based on plagioclase/amphibole Al-Si partitioning and amphibole/liquid Mg partitioning

    NASA Astrophysics Data System (ADS)

    Molina, J. F.; Moreno, J. A.; Castro, A.; Rodríguez, C.; Fershtater, G. B.

    2015-09-01

    Dependencies of plagioclase/amphibole Al-Si partitioning, DAl/Siplg/amp, and amphibole/liquid Mg partitioning, DMgamp/liq, on temperature, pressure and phase compositions are investigated employing robust regression methods based on MM-estimators. A database with 92 amphibole-plagioclase pairs - temperature range: 650-1050 °C; amphibole compositional limits: > 0.02 apfu (23O) Ti and > 0.05 apfu Al - and 148 amphibole-glass pairs - temperature range: 800-1100 °C; amphibole compositional limit: CaM4/(CaM4 + NaM4) > 0.75 - compiled from experiments in the literature was used for the calculations (amphibole normalization scheme: 13-CNK method). Statistical analysis reveals a significant dependence of DAl/Siplg/amp on pressure, temperature, Al fraction in amphibole T1-site, XAlT1, and albite fraction in plagioclase, XAb, leading to the barometric expression:

  3. Cathodoluminescence microscopy and petrographic image analysis of aggregates in concrete pavements affected by alkali-silica reaction

    SciTech Connect

    Stastna, A.; Sachlova, S.; Pertold, Z.; Prikryl, R.; Leichmann, J.

    2012-03-15

    Various microscopic techniques (cathodoluminescence, polarizing and electron microscopy) were combined with image analysis with the aim to determine a) the modal composition and degradation features within concrete, and b) the petrographic characteristics and the geological types (rocks, and their provenance) of the aggregates. Concrete samples were taken from five different portions of Highway Nos. D1, D11, and D5 (the Czech Republic). Coarse and fine aggregates were found to be primarily composed of volcanic, plutonic, metamorphic and sedimentary rocks, as well as of quartz and feldspar aggregates of variable origins. The alkali-silica reaction was observed to be the main degradation mechanism, based upon the presence of microcracks and alkali-silica gels in the concrete. Use of cathodoluminescence enabled the identification of the source materials of the quartz aggregates, based upon their CL characteristics (i.e., color, intensity, microfractures, deformation, and zoning), which is difficult to distinguish only employing polarizing and electron microscopy. - Highlights: Black-Right-Pointing-Pointer ASR in concrete pavements on the Highways Nos. D1, D5 and D11 (Czech Republic). Black-Right-Pointing-Pointer Cathodoluminescence was combined with various microscopic techniques and image analysis. Black-Right-Pointing-Pointer ASR was attributed to aggregates. Black-Right-Pointing-Pointer Source materials of aggregates were identified based on cathodoluminescence characteristics. Black-Right-Pointing-Pointer Quartz comes from different volcanic, plutonic and metamorphic parent rocks.

  4. Evidence for an approximately 4.5 aeon age of plagioclase clasts in a lunar highland breccia

    NASA Technical Reports Server (NTRS)

    Jessberger, E. K.; Huneke, J. C.; Wasserburg, G. J.

    1974-01-01

    Argon from neutron-irradiated mineral separates and whole rock samples of a metamorphosed breccia (65015) from Apollo 16 has been analyzed with a large number of gas extraction steps in order to obtain a high resolution in the apparent ages and to identify the gas released from different sources. The results on plagioclase show a Ar-40/Ar-39 plateau age of 3.98 b.y. which is attributed to the time of metamorphism, and an age of about 4.5 b.y. in the high-temperature fraction. Correlation of the release pattern with Ar-37 instead of Ar-39 permits the association of the approximate 4.5 b.y. age with relict plagioclasts which were demonstrated in previous petrographic and Rb-Sr studies as being unequilibrated. This result suggests that it is possible to identify lithic components which represent the early lunar crust.

  5. Lingunite-a high-pressure plagioclase polymorph at mineral interfaces in doleritic rock of the Lockne impact structure (Sweden)

    NASA Astrophysics Data System (ADS)

    Agarwal, Amar; Reznik, Boris; Kontny, Agnes; Heissler, Stefan; Schilling, Frank

    2016-05-01

    Lingunite nanocrystals and amorphous plagioclase (maskelynite) are identified at the contacts between augite and labradorite wedge-shaped interfaces in the doleritic rocks of the Lockne impact structure in Sweden. The occurrence of lingunite suggests that the local pressure was above 19 GPa and the local temperature overwhelmed 1000 °C. These values are up to 10 times higher than previous values estimated numerically for bulk pressure and temperature. High shock-induced temperatures are manifested by maskelynite injections into microfractures in augite located next to the wedges. We discuss a possible model of shock heterogeneity at mineral interfaces, which may lead to longer duration of the same shock pressure and a concentration of high temperature thus triggering the kinetics of labradorite transformation into lingunite and maskelynite.

  6. Lingunite-a high-pressure plagioclase polymorph at mineral interfaces in doleritic rock of the Lockne impact structure (Sweden)

    PubMed Central

    Agarwal, Amar; Reznik, Boris; Kontny, Agnes; Heissler, Stefan; Schilling, Frank

    2016-01-01

    Lingunite nanocrystals and amorphous plagioclase (maskelynite) are identified at the contacts between augite and labradorite wedge-shaped interfaces in the doleritic rocks of the Lockne impact structure in Sweden. The occurrence of lingunite suggests that the local pressure was above 19 GPa and the local temperature overwhelmed 1000 °C. These values are up to 10 times higher than previous values estimated numerically for bulk pressure and temperature. High shock-induced temperatures are manifested by maskelynite injections into microfractures in augite located next to the wedges. We discuss a possible model of shock heterogeneity at mineral interfaces, which may lead to longer duration of the same shock pressure and a concentration of high temperature thus triggering the kinetics of labradorite transformation into lingunite and maskelynite. PMID:27188436

  7. A Plagioclase Ultraphyric Basalt group in the Neogene flood basalt piles of eastern Iceland: Volcanic architecture and mode of emplacement

    NASA Astrophysics Data System (ADS)

    Oskarsson, B. V.; Riishuus, M. S.

    2013-12-01

    3D photogrammetry in conjunction with ground mapping was applied in order to assess the architecture of a Plagioclase Ultraphyric Basalt (PUB) group in eastern Iceland, namely the Grænavatn group. The ~10 Myr old group is exposed in steep glacially carved fjords and can be traced over 60 km along strike. Two feeder dikes have been found and show that the group erupted along the trend of the dike swarm associated with the Breiddalur central volcano. The group has 9--14 flows where thickest, and thins to about 3--4 flows up-dip to the east within the distance of 15-20 km from the source. We have estimated the volume of the group to exceed 40 km3. The flows have mixed architecture of simple and compound morphology. The flow lobes have thicknesses from 1--24 m and many reach lengths over 1000 m. The surface morphology varies from rubbly to scoriaceous, but is dominantly of pahoehoe style. The internal structure of the lava flows is well preserved and the flows display abundant vesicle cylinders. The modal percentage of An-rich plagioclase macrocrysts varies from 25--50 % and they are in the range of 5--30 mm. The aspect ratio of the group and the nature of the flows indicate fissure-fed eruptions. A thick flow found at the base of the group in various locations seems to record the largest eruption episode in the formation of the group. This phase is also the most abundant in macrocryst. An asymmetric buildup is seen in one location and may have characterized the general buildup of the group. The general morphology of the lava flows suggests low viscous behavior, at odds with the high crystal content. Petrographic observations and mineral chemistry shows that the plagioclase macrocrysts are very calcic (An80-85) and in disequilibrium with the groundmass and plagioclases therein (An50-70). Thus the apparent lava rheology and emplacement of the PUBs was likely achieved due to fast ascent of the magma through the crust and transfer of heat from the primitive macrocrysts

  8. Alkali metal recovery from carbonaceous material conversion process

    DOEpatents

    Sharp, David W.; Clavenna, LeRoy R.; Gorbaty, Martin L.; Tsou, Joe M.

    1980-01-01

    In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced in the gasifier or similar reaction zone, alkali metal constitutents are recovered from the particles by withdrawing and passing the particles from the reaction zone to an alkali metal recovery zone in the substantial absence of molecular oxygen and treating the particles in the recovery zone with water or an aqueous solution in the substantial absence of molecular oxygen. The solution formed by treating the particles in the recovery zone will contain water-soluble alkali metal constituents and is recycled to the conversion process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. Preventing contact of the particles with oxygen as they are withdrawn from the reaction zone and during treatment in the recovery zone avoids the formation of undesirable alkali metal constituents in the aqueous solution produced in the recovery zone and insures maximum recovery of water-soluble alkali metal constituents from the alkali metal residues.

  9. 40Ar/39Ar and cosmic ray exposure ages of plagioclase-rich lithic fragments from Apollo 17 regolith, 78461

    NASA Astrophysics Data System (ADS)

    Das, J. P.; Baldwin, S. L.; Delano, J. W.

    2016-01-01

    Argon isotopic data is used to assess the potential of low-mass samples collected by sample return missions on planetary objects (e.g., Moon, Mars, asteroids), to reveal planetary surface processes. We report the first 40Ar/39Ar ages and 38Ar cosmic ray exposure (CRE) ages, determined for eleven submillimeter-sized (ranging from 0.06 to 1.2 mg) plagioclase-rich lithic fragments from Apollo 17 regolith sample 78461 collected at the base of the Sculptured Hills. Total fusion analysis was used to outgas argon from the lithic fragments. Three different approaches were used to determine 40Ar/39Ar ages and illustrate the sensitivity of age determination to the choice of trapped (40Ar/36Ar)t. 40Ar/39Ar ages range from ~4.0 to 4.4 Ga with one exception (Plag#10). Surface CRE ages, based on 38Ar, range from ~1 to 24 Ma. The relatively young CRE ages suggest recent re-working of the upper few centimeters of the regolith. The CRE ages may result from the effect of downslope movement of materials to the base of the Sculptured Hills from higher elevations. The apparent 40Ar/39Ar age for Plag#10 is >5 Ga and yielded the oldest CRE age (i.e., ~24 Ma). We interpret this data to indicate the presence of parentless 40Ar in Plag#10, originating in the lunar atmosphere and implanted in lunar regolith by solar wind. Based on a chemical mixing model, plagioclase compositions, and 40Ar/39Ar ages, we conclude that lithic fragments originated from Mg-suite of highland rocks, and none were derived from the mare region.

  10. Plagioclase and epidote buffering of cation ratios in mid-ocean ridge hydrothermal fluids: Experimental results in and near the supercritical region

    SciTech Connect

    Berndt, M.E.; Seyfried, W.E. Jr. ); Janecky, D.R. )

    1989-09-01

    Experiments have been performed with Na-Ca-K-Cl fluids of seawater chlorinity and diabase, basalt, and plagioclase bearing mineral mixtures at 350-425{degree}C and 250-400 bars to help constrain hydrothermal alteration processes at mid-ocean ridges. Dissolved Ca, Na, and pH for all experiments responded systematically to differences in dissolved SiO{sub 2} concentrations and the compositions of plagioclase reactants. Diabase alteration at low fluid/rock mass ratios (0.5 to 1) produces fluids undersaturated with respect to quartz during hydration of primary olivine and orthopyroxene, whereas basalt alteration under similar conditions yields fluids slightly supersaturated with respect to quartz during breakdown of glass to smectite and amphibole. Fluid chemistry in all experiments appears to approach a partial equilibrium state with the albite and anorthite components in plagioclase and approaches a pH consistent with plagioclase alteration to epidote. Trace element data from vent fluids, specifically B and Sr, together with major element chemistry, provides evidence that the reaction zone for black-smoker fluids at mid-ocean ridges is composed of only slightly altered diabase and is characterized by small amounts of epidote, nearly fresh plagioclase and clinopyroxene, and partially to completely hydrated olivine and orthopyroxene. Using equilibrium between plagioclase, the dominant reactant, and epidote, the dominant reaction product in experiments, the authors estimate that temperatures in reaction zones are in excess of 375{degree}C for most vent systems. These temperatures are higher than measured vent temperatures, suggesting that hot spring fluids commonly loose heat during ascent to the sea floor.

  11. Adsorption mechanism of mixed cationic/anionic collectors in feldspar-quartz flotation system.

    PubMed

    Vidyadhar, A; Hanumantha Rao, K

    2007-02-15

    The adsorption mechanism of mixed cationic alkyl diamine and anionic sulfonate/oleate collectors at acidic pH values was investigated on microcline and quartz minerals through Hallimond flotation, electrokinetic and diffuse reflectance FTIR studies. In the presence of anionic collectors, neither of the minerals responded to flotation but the diamine flotation of the minerals was observed to be pH and concentration dependent. The presence of sulfonate enhanced the diamine flotation of the minerals by its co-adsorption. The difference in surface charge between the minerals at pH 2 was found to be the basis for preferential feldspar flotation from quartz in mixed diamine/sulfonate collectors. The infrared spectra revealed no adsorption of sulfonate collector when used alone but displayed its co-adsorption as diamine-sulfonate complex when used with diamine. The presence of sulfonate increased the diamine adsorption due to a decrease in the electrostatic head-head repulsion between the adjacent surface ammonium ions and thereby increasing the lateral tail-tail hydrophobic bonds. The mole ratio of diamine/sulfonate was found to be an important factor in the orientation of alkyl chains and thus the flotation response of minerals. The increase in sulfonate concentration beyond diamine concentration leads to the formation of soluble 1:2 diamine-sulfonate complex or precipitate and the adsorption of these species decreased the flotation since the alkyl chains are in chaotical orientation with a conceivable number of head groups directing towards the solution phase.

  12. Accretion and canal impacts in a rapidly subsiding wetland II: Feldspar marker horizon technique

    USGS Publications Warehouse

    Cahoon, D.R.; Turner, R.E.

    1989-01-01

    Recent (6-12 months) marsh sediment accretion and accumulation rates were measured with feldspar marker horizons in the vicinity of natural waterways and man-made canals with spoil banks in the rapidly subsiding environment of coastal Louisiana. Annual accretion rates in a Spartina alterniflora salt marsh in the Mississippi deltaic plain averaged 6 mm in marsh adjacent to canals compared to 10 mm in marsh adjacent to natural waterways. The rates, however, were not statistically significantly different. The average rate of sediment accretion in the same salt marsh region for a transect perpendicular to a canal (13 mm yr-1) was significantly greater than the rate measured for a transect perpendicular to a natural waterway (7 mm yr-1). Measurements of soil bulk density and organic matter content from the two transects were also different. This spatial variability in accretion rates is probably related to (1) spoil bank influences on local hydrology; and (2) a locally high rate of sediment input from lateral erosion associated with pond enlargement. In a brackish Spatina patens marsh on Louisiana's chenier plain, vertical accretion rates were the same along natural and canal waterways (3-4 mm yr-1) in a hydrologically restricted marsh region. However, the accretion rates for both waterways were significantly lower than the rates along a nonhydrologically restricted natural waterway nearby (11 mm yr-1). The vertical accretion of matter displayed semi-annual differences in the brackish marsh environment.

  13. Volcanic rocks of the McDermitt Caldera, Nevada-Oregon

    USGS Publications Warehouse

    Greene, Robert C.

    1976-01-01

    The McDermitt caldera, a major Miocene eruptive center is locatedin the northernmost Great Basin directly west of McDermitt, Nev. The alkali rhyolite of Jordan Meadow was erupted from the caldera and covered an area of about 60,000 sq km; the volume of rhyolite is about 960 cubic km. Paleozoic and Mesozoic sedimentary rocks and Mesozoic granodiorite form the pre-Tertiary Basement in this area.. Overlying these is a series of volcanic rocks, probably all of Miocene age. The lowest is a dacite welded tuff, a reddish-brown rock featuring abundant phenocrysts of plagioclase, hornblende, and biotite; next is a heterogeneous unit consisting of mocks ranging from basalt to dacite. Overlying these is the basalt and andesite of Orevada View, over 700 m thick and consisting of a basal unit of cinder agglutinate overlain by basalt and andesite, much of which contains conspicuous large plagioclase phenocrysts. Near Disaster Peak and Orevada View, the basalt and andesite are overlain by additional units of silicic volcanic rocks. The lower alkali rhyolite welded tuff contains abundant phenocrysts of alkali feldspar and has a vitric phase with obvious pumice and shard texture. The rhyolite of Little Peak consists of a wide variety of banded flows or welded ruffs and breccias, mostly containing abundant alkali feldspar phenocrysts. It extends south from Disaster Peak and apparently underlies the alkali rhyolite of Jordan Meadow. The quartz latite of Sage Creek lies north of Disaster Peak and consists mostly of finely mottled quartz latite with sparse minute plagioclase phenocrysts. Volcanic rock units in the east part of the area near the Cordero mine include trachyandesite, quartz labile of McConnell Canyon, and rhyolite of McCormick Ranch. The trachyandesite is dark gray and contains less than 1 percent microphenocrysts plagioclase. It is the lowest unit exposed and may correlate with part of the basalt and andesite of Orevada View. The quartz latite of McConnell Canyon is

  14. Infrared and Raman spectroscopic studies on alkali borate glasses: evidence of mixed alkali effect.

    PubMed

    Padmaja, G; Kistaiah, P

    2009-03-19

    A lithium-potassium-borate glass system containing manganese and iron cations has been thoroughly investigated in order to obtain information about the mixed alkali effect and the structural role of both the manganese and iron in such glass hosts. Mixed alkali borate glasses of the (30 - x)Li(2)O - xK(2)O - 10CdO/ZnO - 59B(2)O(3) (x = 0, 10, 15, 20, and 30) doped with 1MnO(2)/1Fe(2)O(3) system were prepared by a melt quench technique. The amorphous phase of the prepared glass samples was confirmed from their X-ray diffraction. The spectroscopic properties of glass samples were studied using infrared (IR) and Raman spectroscopic techniques. The density of all the prepared glasses was measured using Archimedes principle. Molar volumes were estimated from the density data. IR spectra of these glasses revealed a dramatic variation of three- and four-coordinated boron structures as a function of mixed alkali concentration. The vibrations due to Li-O, K-O, and MnO(4)/FeO(4) arrangements are consistent in all the compositions and show a nonlinear variation in the intensity with alkali content. Raman spectra of different alkali combinations with CdO and ZnO present drastic changes in the intensity of various Raman bands. The observation of disappearance and reappearance of IR and Raman bands as a function of various alkali concentrations is an important result pertaining to the mixed alkali effect in borate glasses. Acting as complementary spectroscopic techniques, both types of measurements, IR and Raman, revealed that the network structure of the studied glasses is mainly based on BO(3) and BO(4) units placed in different structural groups, the BO(3) units being dominant. The measured IR and Raman spectra of different glasses are used to clarify the optical properties of the present glasses correlating them with their structure and composition. PMID:19235995

  15. Trace element and Pb isotope composition of plagioclase from dome samples from the 2004-2005 eruption of Mount St. Helens, Washington: Chapter 35 in A volcano rekindled: the renewed eruption of Mount St. Helens, 2004-2006

    USGS Publications Warehouse

    Kent, Adam J.R.; Rowe, Michael C.; Thornber, Carl R.; Pallister, John S.; Sherrod, David R.; Scott, William E.; Stauffer, Peter H.

    2008-01-01

    Plagioclase crystals from gabbronorite inclusions in three dacite samples have markedly different trace-element and Pbisotope compositions from those of plagioclase phenocrysts, despite having a similar range of anorthite contents. Inclusions show some systematic differences from each other but typically have higher Ti, Ba, LREE, and Pb and lower Sr and have lower 208Pb/206Pb and 207Pb/206Pb ratios than coexisting plagioclase phenocrysts. The compositions of plagioclase from inclusions cannot be related to phenocryst compositions by any reasonable petrologic model. From this we suggest that they are unlikely to represent magmatic cumulates or restite inclusions but instead are samples of mafic Tertiary basement from beneath the volcano.

  16. Infrared spectra of FHF - in alkali halides

    NASA Astrophysics Data System (ADS)

    Chunnilall, C. J.; Sherman, W. F.

    1982-03-01

    The bifluoride ion, FHF -, has been substitutionally isolated within single crystal samples of several different alkali halides. Infrared spectra of these crystals have been studied for sample temperatures down to 8K when half-bandwidths of less than 1 cm -1 have been observed. (Note that at room temperature ν 3 is observed to have a half-bandwidth of about 40 cm -1). The frequency shifts and half-bandwidth changes caused by cooling are considered together with the frequency shifts caused by pressures up to 10 k bar. The low temperature spectra clearly indicate that FHF - is a linear symmetrical ion when substitutionally isolated within alkali halides of either the NaCl or CsCl structure.

  17. Geopolymers and Related Alkali-Activated Materials

    NASA Astrophysics Data System (ADS)

    Provis, John L.; Bernal, Susan A.

    2014-07-01

    The development of new, sustainable, low-CO2 construction materials is essential if the global construction industry is to reduce the environmental footprint of its activities, which is incurred particularly through the production of Portland cement. One type of non-Portland cement that is attracting particular attention is based on alkali-aluminosilicate chemistry, including the class of binders that have become known as geopolymers. These materials offer technical properties comparable to those of Portland cement, but with a much lower CO2 footprint and with the potential for performance advantages over traditional cements in certain niche applications. This review discusses the synthesis of alkali-activated binders from blast furnace slag, calcined clay (metakaolin), and fly ash, including analysis of the chemical reaction mechanisms and binder phase assemblages that control the early-age and hardened properties of these materials, in particular initial setting and long-term durability. Perspectives for future research developments are also explored.

  18. Removal of Retired Alkali Metal Test Systems

    SciTech Connect

    Brehm, W. F.; Church, W. R.; Biglin, J. W.

    2003-02-26

    This paper describes the successful effort to remove alkali metals, alkali metal residues, and piping and structures from retired non-radioactive test systems on the Hanford Site. These test systems were used between 1965 and 1982 to support the Fast Flux Test Facility and the Liquid Metal Fast Breeder Reactor Program. A considerable volume of sodium and sodium-potassium alloy (NaK) was successfully recycled to the commercial sector; structural material and electrical material such as wiring was also recycled. Innovative techniques were used to safely remove NaK and its residues from a test system that could not be gravity-drained. The work was done safely, with no environmental issues or significant schedule delays.

  19. Alkali Metal Heat Pipe Life Issues

    NASA Technical Reports Server (NTRS)

    Reid, Robert S.

    2004-01-01

    One approach to space fission power system design is predicated on the use of alkali metal heat pipes, either as radiator elements, thermal management components, or as part of the core primary heat-transfer system. This synopsis characterizes long-life core heat pipes. References are included where more detailed information can be found. Specifics shown here are for demonstrational purposes and do not necessarily reflect current Project Prometheus point designs.

  20. Alkali Metal Heat Pipe Life Issues

    SciTech Connect

    Reid, Robert S.

    2004-07-01

    One approach to fission power system design uses alkali metal heat pipes for the core primary heat-transfer system. Heat pipes may also be used as radiator elements or auxiliary thermal control elements. This synopsis characterizes long-life core heat pipes. References are included where information that is more detailed can be found. Specifics shown here are for demonstration purposes and do not necessarily reflect current Nasa Project Prometheus point designs. (author)

  1. Ion Pairing in Alkali Nitrate Electrolyte Solutions.

    PubMed

    Xie, Wen Jun; Zhang, Zhen; Gao, Yi Qin

    2016-03-10

    In this study, we investigate the thermodynamics of alkali nitrate salt solutions, especially the formation of contact ion pairs between alkali cation and nitrate anion. The ion-pairing propensity shows an order of LiNO3 < NaNO3 < KNO3. Such results explain the salt activity coefficients and suggest that the empirical "law of matching water affinity" is followed by these alkali nitrate salt solutions. The spatial patterns of contact ion pairs are different in the three salt solutions studied here: Li(+) forms the contact ion pair with only one oxygen of the nitrate while Na(+) and K(+) can also be shared by two oxygens of the nitrate. In reproducing the salt activity coefficient using Kirkwood-Buff theory, we find that it is essential to include electronic polarization for Li(+) which has a high charge density. The electronic continuum correction for nonpolarizable force field significantly improves the agreement between the calculated activity coefficients and their experimental values. This approach also improves the performance of the force field on salt solubility. From these two aspects, this study suggests that electronic continuum correction can be a promising approach to force-field development for ions with high charge densities. PMID:26901167

  2. Ion Pairing in Alkali Nitrate Electrolyte Solutions.

    PubMed

    Xie, Wen Jun; Zhang, Zhen; Gao, Yi Qin

    2016-03-10

    In this study, we investigate the thermodynamics of alkali nitrate salt solutions, especially the formation of contact ion pairs between alkali cation and nitrate anion. The ion-pairing propensity shows an order of LiNO3 < NaNO3 < KNO3. Such results explain the salt activity coefficients and suggest that the empirical "law of matching water affinity" is followed by these alkali nitrate salt solutions. The spatial patterns of contact ion pairs are different in the three salt solutions studied here: Li(+) forms the contact ion pair with only one oxygen of the nitrate while Na(+) and K(+) can also be shared by two oxygens of the nitrate. In reproducing the salt activity coefficient using Kirkwood-Buff theory, we find that it is essential to include electronic polarization for Li(+) which has a high charge density. The electronic continuum correction for nonpolarizable force field significantly improves the agreement between the calculated activity coefficients and their experimental values. This approach also improves the performance of the force field on salt solubility. From these two aspects, this study suggests that electronic continuum correction can be a promising approach to force-field development for ions with high charge densities.

  3. Transport properties of alkali metal doped fullerides

    SciTech Connect

    Yadav, Daluram Yadav, Nishchhal

    2015-07-31

    We have studied the intercage interactions between the adjacent C{sub 60} cages and expansion of lattice due to the intercalation of alkali atoms based on the spring model to estimate phonon frequencies from the dynamical matrix for the intermolecular alkali-C{sub 60} phonons. We considered a two-peak model for the phonon density of states to investigate the nature of electron pairing mechanism for superconducting state in fullerides. Coulomb repulsive parameter and the electron phonon coupling strength are obtained within the random phase approximation. Transition temperature, T{sub c}, is obtained in a situation when the free electrons in lowest molecular orbital are coupled with alkali-C{sub 60} phonons as 5 K, which is much lower as compared to reported T{sub c} (20 K). The superconducting pairing is mainly driven by the high frequency intramolecular phonons and their effects enhance it to 22 K. The importance of the present study, the pressure effect and normal state transport properties are calculated within the same model leading superconductivity.

  4. Climate dependence of feldspar weathering in shale soils along a latitudinal gradient

    NASA Astrophysics Data System (ADS)

    Dere, Ashlee L.; White, Timothy S.; April, Richard H.; Reynolds, Brian; Miller, Thomas E.; Knapp, Elizabeth P.; McKay, Larry D.; Brantley, Susan L.

    2013-12-01

    Although regolith, the mantle of physically, chemically, and biologically altered material overlying bedrock, covers much of Earth’s continents, the rates and mechanisms of regolith formation are not well quantified. Without this knowledge, predictions of the availability of soil to sustain Earth’s growing population are problematic. To quantify the influence of climate on regolith formation, a transect of study sites has been established on the same lithology - Silurian shale - along a climatic gradient in the northern hemisphere as part of the Susquehanna Shale Hills Critical Zone Observatory, Pennsylvania, USA. The climate gradient is bounded by a cold/wet end member in Wales and a warm/wet end member in Puerto Rico; in between, mean annual temperature (MAT) and mean annual precipitation (MAP) increase to the south through New York, Pennsylvania, Virginia, Tennessee and Alabama. The site in Puerto Rico does not lie on the same shale formation as the Appalachian sites but is similar in composition. Soils and rocks were sampled at geomorphologically similar ridgetop sites to compare and model shale weathering along the transect. Focusing on the low-concentration, non-nutrient element Na, we observe that the extent and depth of Na depletion is greater where mean annual temperature (MAT) and precipitation (MAP) are higher. Na depletion, a proxy for feldspar weathering, is the deepest reaction documented in the augerable soil profiles. This may therefore be the reaction that initiates the transformation of high bulk-density bedrock to regolith of low bulk density. Based on the shale chemistry along the transect, the time-integrated Na release rate (QNa) increases exponentially as a function of MAT and linearly with MAP. NY, the only site with shale-till parent material, is characterized by a QNa that is 18 times faster than PA, an observation which is attributed to the increased surface area of minerals due to grinding of the glacier and kinetically limited

  5. The effect of microbial glucose metabolism on bytownite feldspar dissolution rates between 5 and 35 C

    SciTech Connect

    Welch, S.A.; Ullman, W.J.

    1999-10-01

    The rate of Si release from dissolving bytownite feldspar in abiotic batch reactors increased as temperatures increased from 5 to 35 C. Metabolically inert subsurface bacteria (bacteria in solution with no organic substrate) had no apparent effect on dissolution rates over this temperature range. When glucose was added to the microbial cultures, the bacteria responded by producing gluconic acid, which catalyzed the dissolution reaction by both proton- and ligand-promoted mechanisms. The metabolic production, excretion, and consumption of gluconic acid in the course of glucose oxidation, and therefore, the degree of microbial enhancement of mineral dissolution, depend on temperature. There was little accumulation of gluconic acid and therefore, no significant enhancement of mineral dissolution rates at 35 C compared to the abiotic controls. At 20 C, gluconate accumulated in the experimental solutions only at the beginning of the experiment and led to a twofold increase in dissolved Si release compared to the controls, primarily by the ligand-promoted dissolution mechanism. There was significant accumulation of gluconic acid in the 5 C experiment, which is reflected in a significant reduction in pH, leading to 20-fold increase in Si release, primarily attributable to the proton-promoted dissolution mechanism. These results indicate that bacteria and microbial metabolism can affect mineral dissolution rates in organic-rich, nutrient-poor environments; the impact of microbial metabolism on aluminum silicate dissolution rates may be greater at lower rather than at higher temperatures due to the metabolic accumulation of dissolution-enhancing protons and ligands in solution.

  6. Highly retentive core domains in K-feldspar preserve argon ages from high temperature stages of granite exhumation

    NASA Astrophysics Data System (ADS)

    Forster, Marnie; Lister, Gordon

    2016-04-01

    Retentive core domains are characterized by diffusion parameters that imply K-feldspar should be able to retain argon even at temperatures near or above the granite solidus. In this case it should be possible to date granite emplacement using argon geochronology, and the same answer should be obtained as by using other methods. We present one case study where this is the case, from the elevated Capoas granite stock on Palawan, in the Philippines, and another where it is not, from the South Cyclades Shear Zone, on Ios, Greece. We attempt to determine the factors such as the role of fluid ingress in triggering the in situ recrystallization that can eliminate and/or modify the core domains, leading to relatively youthful ages. Thermochronology is still possible, because less retentive diffusion domains exist, but different methods need to be applied to interpret the data. The work also demonstrates that K-feldspar can be sufficiently retentive as to allow direct dating of processes that reduce the dimensions of diffusion domains, e.g., cataclased and/or recrystallized K-feldspar in fault rock and/or mylonite. These are important developments in the methodology of 40Ar/39Ar geochronology, but to further advance we need to clarify the nature of these highly retentive core domains. In particular, we need better understand how they are modified by microstructural processes during deformation and metamorphism. We need also to assess the role of any crystal structural changes during step-heating in vacuo.

  7. Effect of electrolyte on surface free energy components of feldspar minerals using thin-layer wicking method.

    PubMed

    Karagüzel, C; Can, M F; Sönmez, E; Celik, M S

    2005-05-01

    Application of the thin-layer wicking (TLW) technique on powdered minerals is useful for characterizing their surfaces. Albite (Na-feldspar) and orthoclase (K-feldspar) are feldspar minerals which are frequently found in the same matrix. Despite similarities in their physicochemical properties, separation of these minerals from each other by flotation is generally possible in the presence of monovalent salts such as NaCl. Both albite and orthoclase exhibit the same microflotation properties and rather close electrokinetic profiles in the absence of salt. In this study, contact angles of albite and orthoclase determined by the TLW technique yielded close values in the absence and presence of amine collector. While the calculated surface energies and their components determined using contact angle data reveal that the energy terms remain farther apart in the absence of the collector, the differences narrow down at collector concentrations where full flotation recoveries are obtained. However, the effect of addition of NaCl on contact angles and surface free energy components at constant amine concentration indicates that albite is significantly affected by salt addition, whereas orthoclase remains marginally affected. This interesting finding is explained on the basis of ion-exchange properties, the stability of the interface, flotation data, and zeta potential data in the presence of NaCl.

  8. Alteration of alkali reactive aggregates autoclaved in different alkali solutions and application to alkali-aggregate reaction in concrete (II) expansion and microstructure of concrete microbar

    SciTech Connect

    Lu Duyou . E-mail: duyoulu@njut.edu.cn; Mei Laibao; Xu Zhongzi; Tang Mingshu; Mo Xiangyin; Fournier, Benoit

    2006-06-15

    The effect of the type of alkalis on the expansion behavior of concrete microbars containing typical aggregate with alkali-silica reactivity and alkali-carbonate reactivity was studied. The results verified that: (1) at the same molar concentration, sodium has the strongest contribution to expansion due to both ASR and ACR, followed by potassium and lithium; (2) sufficient LiOH can completely suppress expansion due to ASR whereas it can induce expansion due to ACR. It is possible to use the duplex effect of LiOH on ASR and ACR to clarify the ACR contribution when ASR and ACR may coexist. It has been shown that a small amount of dolomite in the fine-grained siliceous Spratt limestone, which has always been used as a reference aggregate for high alkali-silica reactivity, might dedolomitize in alkaline environment and contribute to the expansion. That is to say, Spratt limestone may exhibit both alkali-silica and alkali-carbonate reactivity, although alkali-silica reactivity is predominant. Microstructural study suggested that the mechanism in which lithium controls ASR expansion is mainly due to the favorable formation of lithium-containing less-expansive product around aggregate particles and the protection of the reactive aggregate from further attack by alkalis by the lithium-containing product layer.

  9. Dynamics of magma supply at Mt. Etna volcano (Southern Italy) as revealed by textural and compositional features of plagioclase phenocrysts

    NASA Astrophysics Data System (ADS)

    Viccaro, Marco; Giacomoni, Pier Paolo; Ferlito, Carmelo; Cristofolini, Renato

    2010-04-01

    A systematic study of textural and compositional zoning (An% and FeO variation) in plagioclase phenocrysts of historic (pre-1971) and recent (post-1971) lavas at Mount Etna was made through back-scattered electron (BSE) images and electron microprobe analyses (EMP). The textures considered include oscillatory zoning and several types of dissolution, resorption and growth textures at the phenocryst cores and/or rims. Two patterns of oscillation were recognized from the combined An-FeO variation: 1) Low Amplitude-High Frequency (LAHF) and 2) High Amplitude-Low Frequency (HALF). The first pattern is interpreted here as due to kinetic effects at the plagioclase/melt interface which developed during crystallization in closed reservoirs. The second, which sometimes involves thin dissolution surfaces marked by irregular edges, angular unconformities and complex dissolution-regrowth patterns, might imply crystallization in a more dynamic regime, probably driven by chemical and physical gradients of the system (e.g., convection in a steadily degassing open-conduit). Dissolution and resorption textures at the core vary from patchy (exclusive to plagioclases within pre-1971 lavas) to strongly sieved, and can be related to increasing rates of decompression under H 2O-undersaturated conditions. Thick sieve-textured envelopes at the phenocryst rims, generally coupled with marked An-FeO increase, result from mixing with more primitive and volatile-rich magmas. In the same crystals from recent activity, An and, to a lesser extent, FeO increase, consistent with the mixing of H 2O-rich magmas similar in their mafic character to the resident magma (cryptic mixing). Two types of growth textures were also recognized at the crystal rims: 1) stripes of regularly-shaped melt inclusions and 2) swallow-tailed, skeletal crystals. In the first instance, the concordant An-FeO decrease suggests crystallization caused by fast ascent-related decompression accompanied by volatile loss. In the

  10. Plagioclase zonation styles in hornblende gabbro inclusions from Little Glass Mountain, Medicine Lake volcano, California: Implications for fractionation mechanisms and the formation of composition gaps

    USGS Publications Warehouse

    Brophy, J.G.; Dorais, M.J.; Donnelly-Nolan, J.; Singer, B.S.

    1997-01-01

    The rhyolite of Little Glass Mountain (73-74% SiO2) is a single eruptive unit that contains inclusions of quenched andesite liquid (54-61% SiO2) and partially crystalline cumulate hornblende gabbro (53-55% SiO2). Based on previous studies, the quenched andesite inclusions and host rhyolite lava are related to one another through fractional crystallization and represent an example of a fractionation-generated composition gap. The hornblende gabbros represent the cumulate residue associated with the rhyolite-producing and composition gap-forming fractionation event. This study combines textural (Nomarski Differential Interference Contrast, NDIC, imaging), major element (An content) and trace element (Mg, Fe, Sr, K, Ti, Ba) data on the style of zonation of plagioclase crystals from representative andesite and gabbro inclusions, to assess the physical environment in which the fractionation event and composition gap formation took place. The andesite inclusions (54-61% SiO2) are sparsely phyric with phenocrysts of plagioclase, augite and Fe-oxide??olivine, +/-orthopyroxene, +/-hornblende set within a glassy to crystalline matrix. The gabbro cumulates (53-55% SiO2) consist of an interconnected framework of plagioclase, augite, olivine, orthopyroxene, hornblende and Fe-oxide along with highly vesicular interstitial glass (70-74% SiO2). The gabbros record a two-stage crystallization history of plagioclase + olivine + augite (Stage I) followed by plagioclase+orthopyroxene + hornblende + Fe-oxide (Stage II). Texturally, the plagioclase crystals in the andesite inclusions are characterized by complex, fine-scale oscillatory zonation and abundant dissolution surfaces. Compositionally (An content) the crystals are essentially unzoned from core-to-rim. These features indicate growth within a dynamic (convecting?), reservoir of andesite magma. In contrast, the plagioclase crystals in the gabbros are texturally smooth and featureless with strong normal zonation from An74 at the

  11. Dry and Wet Friction of Plagioclase: Pure Cataclastic Flow(CF) vs. CF with Concurrent Pressure Solution

    NASA Astrophysics Data System (ADS)

    He, C.; Tan, W.

    2015-12-01

    To distinguish different deformation mechanisms at hydrothermal conditions, friction experiments of plagioclase under nominally dry conditions were compared with that at hydrothermal conditions documented in a previous study[He et al.,2013]. Preliminary result[Tan and He, 2008] shows that the rate dependence of plagioclase under confining pressure of 150MPa and nominally dry conditions is velocity strengthening at temperatures of 50-600oC, in contrast to the full velocity weakening at hydrothermal conditions. Here a) we conducted data fitting to the rate and state friction law to compare with the hydrothermal case; b) microstructural comparison was performed to understand the difference between the dry and wet conditions in the operative deformation mechanisms. The evolution effect (b value) under dry conditions exhibits much smaller values than that at wet conditions, and in contrast to the increasing trend at wet conditions, b values under dry conditions have a decreasing trend as temperature increases, from ~0.007 at 300oC down to 0 at 600oC. The direct effect (a value) at dry conditions has a peak of ~0.01 at 300oC and decreases to a level of 0.007-0.008 at higher temperatures, in contrast to the increasing trend seen at hydrothermal conditions. In the dry case, microstructure at temperatures of 300-600oC transitions gradually from a fabric characterized by localized Riedel shear zones to pervasive shear deformation, with the grain size reduced to a level of 1-3 micron in a submicron matrix in the latter case, corresponding to a lower porosity. The close association between porosity evolution and that of state variable revealed in previous studies[Morrow and Byerlee, 1989; Marone et al.,1990] suggests that the porosity change contributes largely to the evolution effect in addition to plasticity at intergranular contacts, probably due to gradual switching between different densities of packing. Our dry experiments indicate a cataclastic flow where the evolution

  12. Method for the safe disposal of alkali metal

    DOEpatents

    Johnson, Terry R.

    1977-01-01

    Alkali metals such as those employed in liquid metal coolant systems can be safely reacted to form hydroxides by first dissolving the alkali metal in relatively inert metals such as lead or bismuth. The alloy thus formed is contacted with a molten salt including the alkali metal hydroxide and possibly the alkali metal carbonate in the presence of oxygen. This oxidizes the alkali metal to an oxide which is soluble within the molten salt. The salt is separated and contacted with steam or steam-CO.sub.2 mixture to convert the alkali metal oxide to the hydroxide. These reactions can be conducted with minimal hydrogen evolution and with the heat of reaction distributed between the several reaction steps.

  13. Increased mantle heat flow with on-going rifting of the West Antarctic rift system inferred from characterisation of plagioclase peridotite in the shallow Antarctic mantle

    NASA Astrophysics Data System (ADS)

    Martin, A. P.; Cooper, A. F.; Price, R. C.

    2014-03-01

    The lithospheric, and shallow asthenospheric, mantle in Southern Victoria Land are known to record anomalously high heat flow but the cause remains imperfectly understood. To address this issue plagioclase peridotite xenoliths have been collected from Cenozoic alkalic igneous rocks at three localities along a 150 km transect across the western shoulder of the West Antarctic rift system in Southern Victoria Land, Antarctica. There is a geochemical, thermal and chronological progression across this section of the rift shoulder from relatively hot, young and thick lithosphere in the west to cooler, older and thinner lithosphere in the east. Overprinting this progression are relatively more recent mantle refertilising events. Melt depletion and refertilisation was relatively limited in the lithospheric mantle to the west but has been more extensive in the east. Thermometry obtained from orthopyroxene in these plagioclase peridotites indicates that those samples most recently affected by refertilising melts have attained the highest temperatures, above those predicted from idealised dynamic rift or Northern Victoria Land geotherms and higher than those prevailing in the equivalent East Antarctic mantle. Anomalously high heat flow can thus be attributed to entrapment of syn-rift melts in the lithosphere, probably since regional magmatism commenced at least 24 Myr ago. The chemistry and mineralogy of shallow plagioclase peridotite mantle can be explained by up to 8% melt extraction and a series of refertilisation events. These include: (a) up to 8% refertilisation by a N-MORB melt; (b) metasomatism involving up to 1% addition of a subduction-related component; and (c) addition of ~ 1.5% average calcio-carbonatite. A high MgO group of clinopyroxenes can be modelled by the addition of up to 1% alkalic melt. Melt extraction and refertilisation mainly occurred in the spinel stability field prior to decompression and uplift. In this region mantle plagioclase originates by a

  14. Crystal residence times from trace element zoning in plagioclase reveal changes in magma transfer dynamics at Mt. Etna during the last 400 years

    NASA Astrophysics Data System (ADS)

    Viccaro, Marco; Barca, Donatella; Bohrson, Wendy A.; D'Oriano, Claudia; Giuffrida, Marisa; Nicotra, Eugenio; Pitcher, Bradley W.

    2016-04-01

    Trace element zoning in plagioclase of selected alkaline lavas from the historic (1607-1892 AD) and recent (1983-2013 AD) activity of Mt. Etna volcano has been used to explore the possible role that volcano-tectonics exert on magma transfer dynamics. The observed textural characteristics of crystals include near-equilibrium textures (i.e., oscillatory zoning) and textures with variable extent of disequilibrium (patchy zoning, coarse sieve textures and dissolved cores). Historic crystals exhibit lower K concentrations at lower anorthite contents, a feature in agreement with the general more potassic character of the recent lavas if compared to the historic products. Historic plagioclases have statistically higher Ba and lower Sr concentrations than the recent crystals, which result in different Sr/Ba ratios for the two suites of plagioclase. Variations in the anorthite content along core-to-rim profiles obtained on crystals with different types of textures for both the historic and recent eruptive periods were evaluated particularly versus Sr/Ba. At comparable average An contents, crystals characterized by oscillatory zoning, which are representative of near-equilibrium crystallization from the magma, display distinct Sr/Ba ratios. We suggest that these features are primarily related to recharge of a new, geochemically-distinct magma into the storage and transport system of the volcano. In addition to distinct trace element and textural characteristics of plagioclase, Sr diffusion modeling for plagioclase suggests that residence times are generally shorter for crystals found in recently erupted lavas (25-77 years, average 43 years) compared to those of the historic products (43-163 years, average 99 years). Shorter residences times correlate with gradual increases in eruption volume and eruption frequency rates through time. We attribute these features to an increasing influence, since the 17th century, of extensional tectonic structures within the upper 10 km of

  15. Determination of the common and rare alkalies in mineral analysis

    USGS Publications Warehouse

    Wells, R.C.; Stevens, R.E.

    1934-01-01

    Methods are described which afford a determination of each member of the alkali group and are successful in dealing with the quantities of the rare alkalies found in rocks and minerals. The procedures are relatively rapid and based chiefly on the use of chloroplatinic acid, absolute alcohol and ether, and ammonium sulfate. The percentages of all the alkalies found in a number of minerals are given.

  16. Environmental mercury contamination around a chlor-alkali plant

    SciTech Connect

    Lodenius, M.; Tulisalo, E.

    1984-04-01

    The chlor-alkali industry is one of the most important emitters of mercury. This metal is effectively spread from chlor-alkali plants into the atmosphere and it has been reported that only a few percent of the mercury emissions are deposited locally the major part spreading over very large areas. The purpose of this investigation was to study the spreading of mercury up to 100 km from a chlor-alkali plant using three different biological indicators.

  17. Solvation at nanoscale: Alkali-halides in water clusters

    SciTech Connect

    Partanen, Leena; Mikkelae, Mikko-Heikki; Huttula, Marko; Tchaplyguine, Maxim; Zhang Chaofan; Andersson, Tomas; Bjoerneholm, Olle

    2013-01-28

    The solvation of alkali-halides in water clusters at nanoscale is studied by photoelectron spectroscopy using synchrotron radiation. The Na 2p, K 3p, Cl 2p, Br 3d, and I 4d core level binding energies have been measured for salt-containing water clusters. The results have been compared to those of alkali halide clusters and the dilute aqueous salt solutions. It is found that the alkali halides dissolve in small water clusters as ions.

  18. Alkali cation specific adsorption onto fcc(111) transition metal electrodes.

    PubMed

    Mills, J N; McCrum, I T; Janik, M J

    2014-07-21

    The presence of alkali cations in electrolyte solutions is known to impact the rate of electrocatalytic reactions, though the mechanism of such impact is not conclusively determined. We use density functional theory (DFT) to examine the specific adsorption of alkali cations to fcc(111) electrode surfaces, as specific adsorption may block catalyst sites or otherwise impact surface catalytic chemistry. Solvation of the cation-metal surface structure was investigated using explicit water models. Computed equilibrium potentials for alkali cation adsorption suggest that alkali and alkaline earth cations will specifically adsorb onto Pt(111) and Pd(111) surfaces in the potential range of hydrogen oxidation and hydrogen evolution catalysis in alkaline solutions.

  19. High temperature alkali corrosion of ceramics in coal gas

    SciTech Connect

    Pickrell, G.R.; Sun, T.; Brown, J.J.

    1992-05-27

    High temperature alkali corrosion has been known to cause premature failure of ceramic components used in advanced high temperature coal combustion systems such as coal gasification and clean-up, coal fired gas turbines, and high efficiency heat engines. The objective of this research is to systematically evaluate the alkali corrosion resistance of the most commonly used structural ceramics including silicon carbide, silicon nitride, cordierite, mullite, alumina, aluminum titanate, zirconia, and fireclay glass. The study consists of identification of the alkali reaction products (phase equilibria) and the kinetics of the alkali reactions as a function of temperature and time.

  20. High temperature alkali corrosion of ceramics in coal gas

    SciTech Connect

    Pickrell, G.R.; Sun, T.; Brown, J.J.

    1991-11-30

    High temperature alkali corrosion has been known to cause premature failure of ceramic components used in advanced high temperature coal combustion systems such as coal gasification and clean-up, coal fired gas turbines, and high efficiency heat engines. The objective of this program is to systematically evaluate the alkali corrosion resistance of the most commonly used structural ceramics including silicon carbide, silicon nitride, cordierite, mullite, alumina, aluminum titanate, zirconia, and fireclay glass. The study consists of identification of the alkali reaction products (phase equilibria) and the kinetics of the alkali reactions as a function of temperature and time.

  1. High temperature alkali corrosion of ceramics in coal gas

    SciTech Connect

    Pickrell, G.R.; Sun, T.; Brown, J.J.

    1992-08-29

    High temperature alkali corrosion has been known to cause premature failure of ceramic components used in advanced high temperature coal combustion systems such as coal gasification and clean-up, coal fired gas turbines, and high efficiency heat engines. The objective of this research is to systematically evaluate the alkali corrosion resistance of the most commonly used structural ceramics including silicon carbide, silicon nitride, cordierite, mullite, alumina, aluminum titanate, zirconia, and fireclay glass. The study consists of identification of the alkali reaction products (phase equilibria) and the kinetics of the alkali reactions as a function of temperature and time.

  2. Electrochemical devices utilizing molten alkali metal electrode-reactant

    DOEpatents

    Hitchcock, D.C.; Mailhe, C.C.; De Jonghe, L.C.

    1985-07-10

    Electrochemical cells are provided with a reactive metal to reduce the oxide of the alkali metal electrode-reactant. Cells employing a molten alkali metal electrode, e.g., sodium, in contact with a ceramic electrolyte, which is a conductor of the ions of the alkali metal forming the electrode, exhibit a lower resistance when a reactive metal, e.g., vanadium, is allowed to react with and reduce the alkali metal oxide. Such cells exhibit less degradation of the electrolyte and of the glass seals often used to joining the electrolyte to the other components of the cell under cycling conditions.

  3. Electrochemical devices utilizing molten alkali metal electrode-reactant

    DOEpatents

    Hitchcock, David C.; Mailhe, Catherine C.; De Jonghe, Lutgard C.

    1986-01-01

    Electrochemical cells are provided with a reactive metal to reduce the oxide of the alkali metal electrode-reactant. Cells employing a molten alkali metal electrode, e.g., sodium, in contact with a ceramic electrolyte, which is a conductor of the ions of the alkali metal forming the electrode, exhibit a lower resistance when a reactive metal, e.g., vanadium, is allowed to react with and reduce the alkali metal oxide. Such cells exhibit less degradation of the electrolyte and of the glass seals often used to joining the electrolyte to the other components of the cell under cycling conditions.

  4. Microstructural evidence for the transition from dislocation creep to dislocation-accommodated grain boundary sliding in naturally deformed plagioclase

    NASA Astrophysics Data System (ADS)

    Miranda, Elena A.; Hirth, Greg; John, Barbara E.

    2016-11-01

    We use quantitative microstructural analysis including misorientation analysis based on electron backscatter diffraction (EBSD) data to investigate deformation mechanisms of naturally deformed plagioclase in an amphibolite gabbro mylonite. The sample is from lower oceanic crust exposed near the Southwest Indian Ridge, and it has a high ratio of recrystallized matrix grains to porphyroclasts. Microstructures preserved in porphyroclasts suggest that early deformation was achieved principally by dislocation creep with subgrain rotation recrystallization; recrystallized grain (average diameter ∼8 μm) microstructures indicate that subsequent grain boundary sliding (GBS) was active in the continued deformation of the recrystallized matrix. The recrystallized matrix shows four-grain junctions, randomized misorientation axes, and a shift towards higher angles for neighbor-pair misorientations, all indicative of GBS. The matrix grains also exhibit a shape preferred orientation, a weak lattice preferred orientation consistent with slip on multiple slip systems, and intragrain microstructures indicative of dislocation movement. The combination of these microstructures suggest deformation by dislocation-accommodated GBS (DisGBS). Strain localization within the recrystallized matrix was promoted by a transition from grain size insensitive dislocation creep to grain size sensitive GBS, and sustained by the maintenance of a small grain size during superplasticity.

  5. Formation of andesite melts and Ca-rich plagioclase in the submarine Monowai volcanic system, Kermadec arc

    NASA Astrophysics Data System (ADS)

    Kemner, Fabian; Haase, Karsten M.; Beier, Christoph; Krumm, Stefan; Brandl, Philipp A.

    2015-12-01

    Andesites are typical rocks of island arcs and may either form by fractional crystallization processes or by mixing between a mafic and a felsic magma. Here we present new petrographic and geochemical data from lavas of the submarine Monowai volcanic system in the northern Kermadec island arc that display a continuous range in composition from basalt to andesite. Using petrology, major, trace, and volatile element data, we show that basaltic magmas mostly evolve to andesitic magmas by fractional crystallization. Our thermobarometric calculations indicate that the formation of the large caldera is related to eruption of basaltic-andesitic to andesitic magmas from a magma reservoir in the deeper crust. Small variations in trace element ratios between the caldera and the large active cone imply a homogeneous mantle source. Contrastingly, resurgent dome melts of the caldera stagnated at shallower depths are more depleted and show a stronger subduction input than the other edifices. The Monowai basaltic glasses contain less than 1 wt % H2O and follow typical tholeiitic fractionation trends. High-An plagioclase crystals observed in the Monowai lavas likely reflect mixing of H2O-saturated melt batches with hot and dry tholeiitic, decompression melt batches. The result is a relatively H2O-poor mafic magma at Monowai implying that partial melting of the mantle wedge is only partly due to the volatile flux and that adiabatic melting may play a significant role in the formation of the parental melts of the Monowai volcanic system and possibly other arc volcanoes.

  6. Thermobarometry for spinel lherzolite xenoliths in alkali basalts

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

    Application of geothermobarometers to peridotite xenoliths has been providing very useful information on thermal and chemical structure of lithospheric or asthenospheric mantle at the time of almost instantaneous sampling by the host magmas, based on which various thermal (e.g., McKenzie et al., 2005), chemical (e.g., Griffin et al., 2003), and rheological (e.g., Ave Lallemant et al., 1980) models of lithosphere have been constructed. Geothermobarometry for garnet or plagioclase-bearing lithologies provide accurate pressure estimation, but this is not the case for the spinel peridotites, which are frequently sampled from Phanerozoic provinces in various tectonic environments (Nixon and Davies, 1987). There are several geobarometers proposed for spinel lherzolite, such as single pyroxene geothermobarometer (Mercier, 1980) and geothermobarometer based on Ca exchange between olivine and clinopyroxene (Köhler and Brey, 1990), but they have essential problems and it is usually believed that appropriated barometers do not exist for spinel lherzolites (O'Reilly et al., 1997; Medaris et al., 1999). It is thus imperative to develop reliable barometry for spinel peridotite xenoliths. We have developed barometry for spinel peridotite xenoliths by exploiting small differences in pressure dependence in relevant reactions, whose calibration was made through careful evaluation of volume changes of the reactions. This is augmented with higher levels of care in application of barometer by choosing mineral domains and their chemical components that are in equilibrium as close as possible. This is necessary because such barometry is very sensitive to changes in chemical composition induced by transient state of the system possibly owing to pressure and temperature changes as well as chemical modification, forming chemical heterogeneity or zoning frequently reported from various mantle xenoliths (Smith, 1999). Thus very carful treatment of heterogeneity, which might be trivial for

  7. Correlation of the Na/K ratio in geothermal well waters with the thermodynamic properties of low albite and potash feldspar

    SciTech Connect

    Apps, J.A.; Chang, G.M.

    1992-03-01

    The Na/K ratio in geothermal well waters provides a better estimate of the relative stability of low albite and potash feldspar than do predictions from calorimetry and high temperature phase equilibria. The calculated saturation indices from field data for low albite, potash feldspar suggest that [Delta]G[sub f,298][sup o] for the latter should be revised to [minus]3748.6[plus minus]3.7 kJ.mol[sup [minus]1].

  8. Correlation of the Na/K ratio in geothermal well waters with the thermodynamic properties of low albite and potash feldspar

    SciTech Connect

    Apps, J.A.; Chang, G.M.

    1992-03-01

    The Na/K ratio in geothermal well waters provides a better estimate of the relative stability of low albite and potash feldspar than do predictions from calorimetry and high temperature phase equilibria. The calculated saturation indices from field data for low albite, potash feldspar suggest that {Delta}G{sub f,298}{sup o} for the latter should be revised to {minus}3748.6{plus_minus}3.7 kJ.mol{sup {minus}1}.

  9. Thermal diffusivity of pyroxene, feldspar, and silica melts, glasses, and single-crystals at high temperature

    NASA Astrophysics Data System (ADS)

    Pertermann, M.; Branlund, J.; Whittington, A.; Hofmeister, A.

    2007-12-01

    Thermal diffusivity (D) due to phonon transport (the lattice component) was measured using laser-flash analysis from oriented single-crystals and of glasses above the glass transition, which proxy as melts. Compositions include SiO2, CaMgSi2O6, LiAlSi2O6, NaAlSi3O8, and CaAl2Si2O8. KAlSi3O8 was studied previously. Viscosity measurements of the supercooled liquids, in the range 106.8 to 1012.3 Pas, confirm near-Arrhenian behavior. For all compositions and for crystal and glass, D decreases with T, approaching a constant generally near 1000 K: Dsat, which is larger in the crystal than in the glass. A rapid decrease in D as T is increased further (ca 1400 K for orthoclase) is consistent with crossing the glass transition, verified from our viscosity data on these systems. The amount of the decrease depends on the chemical composition and similar to the relative decrease observed in heat capacity. Orthoclase values for Dsat are 0.65± 0.3 mm2/s for bulk crystal and 0.53+/-0.03 mm2/s for the glass. Constant D = 0.475+/-.01 mm2/s represents melt. Thermal conductivity (klat) of orthoclase glass, calculated using previous results for heat capacity (CP) and our density data, increases with T due to CP strongly increasing with T, reaching a plateau near 1.45 W/m-K for melt, but is always below klat of the crystal. Similar results were obtained from the other systems studied. Melting of silica, pyroxene, and feldspars impedes heat transport, providing positive thermal feedback that may promote further melting in the continental crust. The consistency of the behavior for these different compositions and structures suggests that our results are universal, holding for oceanic lithosphere as well. Melts, due to being disordered, are poor transporters of heat via vibrations. However, d(ln klat)/dP depends inversely on bulk modulus, suggesting that at some high pressure, the thermal conductivity of the melt and corresponding crystal become equal so that retention of heat by melts

  10. Frictional Properties of Feldspar and Quartz at the Temperatures of Seismogenic Zone

    NASA Astrophysics Data System (ADS)

    Arai, T.; Masuda, K.; Takahashi, M.; Fujimoto, K.; Shigematsu, N.; Sumii, T.; Okuyama, Y.

    2003-12-01

    Most of earthquakes in the crust occurred at the depth of 5 to 20km, and temperatures of 100 to 350° C. The physical properties of rocks at around these temperatures were determined by many frictional experiments. These results indicated the velocity dependence of steady state friction (a-b) was switched from velocity weakening ( seismic slip ) to velocity strengthening ( aseismic slip ) at around 350° C in the wet condition. In these experimental studies, granites were generally used. On the other hand, it is important to evaluate and to compare the physical properties of each mineral which composed of crustal rocks, for example feldspar and quartz, in order to understand the source processes of earthquakes in detail. In this study, we conducted frictional experiments by using albite, anorthite, and quartz gouges ( about 3μ m diameter ) under high pressure and high temperature in a triaxial apparatus, and compared frictional behaviors of three minerals with elevated temperature under the wet and dry conditions. These experiments were conducted by the velocity-stepping test. Temperature varied from room temperature to 600° C. In the dry conditions, experiments were conducted under the confining pressure of 150MPa. In the wet conditions, pore water pressure was applied up to 50MPa under the confining pressure of 200MPa. Sample was put between upper and lower sawcut alumina cylinders ( 20mm diameter x 40mm long ). The sawcut was oriented at 30° to the loading axis. These were jacketed with thin sleeves of annealed Cu. The values for a-b of quartz and albite were positive under the dry condition from room temperature to 600° C. On the other hand, those values of albite and quartz were negative at the temperature of 200° C and 300° C under the wet condition respectively. Those values of quartz decreased as the temperature increased from 100° C to 300° C and increased as the temperature increased from 300° C to 600° C. Those values of albite were switched

  11. Cathode architectures for alkali metal / oxygen batteries

    SciTech Connect

    Visco, Steven J; Nimon, Vitaliy; De Jonghe, Lutgard C; Volfkovich, Yury; Bograchev, Daniil

    2015-01-13

    Electrochemical energy storage devices, such as alkali metal-oxygen battery cells (e.g., non-aqueous lithium-air cells), have a cathode architecture with a porous structure and pore composition that is tailored to improve cell performance, especially as it pertains to one or more of the discharge/charge rate, cycle life, and delivered ampere-hour capacity. A porous cathode architecture having a pore volume that is derived from pores of varying radii wherein the pore size distribution is tailored as a function of the architecture thickness is one way to achieve one or more of the aforementioned cell performance improvements.

  12. Electrodes For Alkali-Metal Thermoelectric Converters

    NASA Technical Reports Server (NTRS)

    Williams, Roger M.; Wheeler, Bob L.; Jeffries-Nakamura, Barbara; Lamb, James L.; Bankston, C. Perry; Cole, Terry

    1989-01-01

    Combination of thin, porous electrode and overlying collector grid reduces internal resistance of alkali-metal thermoelectric converter cell. Low resistance of new electrode and grid boosts power density nearly to 1 W/cm2 of electrode area at typical operating temperatures of 1,000 to 1,300 K. Conductive grid encircles electrode film on alumina tube. Bus wire runs along tube to collect electrical current from grid. Such converters used to transform solar, nuclear, and waste heat into electric power.

  13. High power diode pumped alkali vapor lasers

    NASA Astrophysics Data System (ADS)

    Zweiback, J.; Krupke, B.

    2008-05-01

    Diode pumped alkali lasers have developed rapidly since their first demonstration. These lasers offer a path to convert highly efficient, but relatively low brightness, laser diodes into a single high power, high brightness beam. General Atomics has been engaged in the development of DPALs with scalable architectures. We have examined different species and pump characteristics. We show that high absorption can be achieved even when the pump source bandwidth is several times the absorption bandwidth. In addition, we present experimental results for both potassium and rubidium systems pumped with a 0.2 nm bandwidth alexandrite laser. These data show slope efficiencies of 67% and 72% respectively.

  14. (abstract) Fundamental Mechanisms of Electrode Kinetics and Alkali Metal Atom Transport at the Alkali Beta'-Alumina/Porous Electrode/Alkali Metal Vapor Three Phase Boundary

    NASA Technical Reports Server (NTRS)

    Williams, R. M.; Jeffries-Nakamura, B.; Ryan, M. A.; Underwood, M. L.; O'Connor, D.; Kisor, A.; Kikkert, S. K.

    1993-01-01

    The mechanisms of electrode kinetics and mass transport of alkali metal oxidation and alkali metal cation reduction at the solid electrolyte/porous electrode boundary as well as alkali metal transport through porous metal electrodes has important applications in optimizing device performance in alkali metal thermal to electric converter (AMTEC) cells which are high temperature, high current density electrochemical cells. Basic studies of these processes also affords the opportunity to investigate a very basic electrochemical reaction over a wide range of conditions; and a variety of mass transport modes at high temperatures via electrochemical techniques. The temperature range of these investigations covers 700K to 1240K; the alkali metal vapor pressures range from about 10(sup -2) to 10(sup 2) Pa; and electrodes studied have included Mo, W, Mo/Na(sub 2)MoO(sub 4), W/Na(sub 2)WO(sub 4), WPt(sub x), and WRh(sub x) (1.0 < x < 6.0 ) with Na at Na-beta'-alumina, and Mo with K at K-beta'-alumina. Both liquid metal/solid electrolyte/alkali metal vapor and alkali metal vapor/solid electrolyte/vapor cells have been used to characterize the reaction and transport processes. We have previously reported evidence of ionic, free molecular flow, and surface transport of sodium in several types of AMTEC electrodes.

  15. Elucidation of transport mechanism and enhanced alkali ion transference numbers in mixed alkali metal-organic ionic molten salts.

    PubMed

    Chen, Fangfang; Forsyth, Maria

    2016-07-28

    Mixed salts of Ionic Liquids (ILs) and alkali metal salts, developed as electrolytes for lithium and sodium batteries, have shown a remarkable ability to facilitate high rate capability for lithium and sodium electrochemical cycling. It has been suggested that this may be due to a high alkali metal ion transference number at concentrations approaching 50 mol% Li(+) or Na(+), relative to lower concentrations. Computational investigations for two IL systems illustrate the formation of extended alkali-anion aggregates as the alkali metal ion concentration increases. This tends to favor the diffusion of alkali metal ions compared with other ionic species in electrolyte solutions; behavior that has recently been reported for Li(+) in a phosphonium ionic liquid, thus an increasing alkali transference number. The mechanism of alkali metal ion diffusion via this extended coordination environment present at high concentrations is explained and compared to the dynamics at lower concentrations. Heterogeneous alkali metal ion dynamics are also evident and, somewhat counter-intuitively, it appears that the faster ions are those that are generally found clustered with the anions. Furthermore these fast alkali metal ions appear to correlate with fastest ionic liquid solvent ions. PMID:27375042

  16. Superconductivity in alkali metal intercalated iron selenides.

    PubMed

    Krzton-Maziopa, A; Svitlyk, V; Pomjakushina, E; Puzniak, R; Conder, K

    2016-07-27

    Alkali metal intercalated iron selenide superconductors A x Fe2-y Se2 (where A  =  K, Rb, Cs, Tl/K, and Tl/Rb) are characterized by several unique properties, which were not revealed in other superconducting materials. The compounds crystallize in overall simple layered structure with FeSe layers intercalated with alkali metal. The structure turned out to be pretty complex as the existing Fe-vacancies order below ~550 K, which further leads to an antiferromagnetic ordering with Néel temperature fairly above room temperature. At even lower temperatures a phase separation is observed. While one of these phases stays magnetic down to the lowest temperatures the second is becoming superconducting below ~30 K. All these effects give rise to complex relationships between the structure, magnetism and superconductivity. In particular the iron vacancy ordering, linked with a long-range magnetic order and a mesoscopic phase separation, is assumed to be an intrinsic property of the system. Since the discovery of superconductivity in those compounds in 2010 they were investigated very extensively. Results of the studies conducted using a variety of experimental techniques and performed during the last five years were published in hundreds of reports. The present paper reviews scientific work concerning methods of synthesis and crystal growth, structural and superconducting properties as well as pressure investigations. PMID:27248118

  17. Durability of Alkali Activated Blast Furnace Slag

    NASA Astrophysics Data System (ADS)

    Ellis, K.; Alharbi, N.; Matheu, P. S.; Varela, B.; Hailstone, R.

    2015-11-01

    The alkali activation of blast furnace slag has the potential to reduce the environmental impact of cementitious materials and to be applied in geographic zones where weather is a factor that negatively affects performance of materials based on Ordinary Portland Cement. The scientific literature provides many examples of alkali activated slag with high compressive strengths; however research into the durability and resistance to aggressive environments is still necessary for applications in harsh weather conditions. In this study two design mixes of blast furnace slag with mine tailings were activated with a potassium based solution. The design mixes were characterized by scanning electron microscopy, BET analysis and compressive strength testing. Freeze-thaw testing up to 100 freeze-thaw cycles was performed in 10% road salt solution. Our findings included compressive strength of up to 100 MPa after 28 days of curing and 120 MPa after freeze-thaw testing. The relationship between pore size, compressive strength, and compressive strength after freeze-thaw was explored.

  18. Superconductivity in alkali metal intercalated iron selenides.

    PubMed

    Krzton-Maziopa, A; Svitlyk, V; Pomjakushina, E; Puzniak, R; Conder, K

    2016-07-27

    Alkali metal intercalated iron selenide superconductors A x Fe2-y Se2 (where A  =  K, Rb, Cs, Tl/K, and Tl/Rb) are characterized by several unique properties, which were not revealed in other superconducting materials. The compounds crystallize in overall simple layered structure with FeSe layers intercalated with alkali metal. The structure turned out to be pretty complex as the existing Fe-vacancies order below ~550 K, which further leads to an antiferromagnetic ordering with Néel temperature fairly above room temperature. At even lower temperatures a phase separation is observed. While one of these phases stays magnetic down to the lowest temperatures the second is becoming superconducting below ~30 K. All these effects give rise to complex relationships between the structure, magnetism and superconductivity. In particular the iron vacancy ordering, linked with a long-range magnetic order and a mesoscopic phase separation, is assumed to be an intrinsic property of the system. Since the discovery of superconductivity in those compounds in 2010 they were investigated very extensively. Results of the studies conducted using a variety of experimental techniques and performed during the last five years were published in hundreds of reports. The present paper reviews scientific work concerning methods of synthesis and crystal growth, structural and superconducting properties as well as pressure investigations.

  19. Superconductivity in alkali metal intercalated iron selenides

    NASA Astrophysics Data System (ADS)

    Krzton-Maziopa, A.; Svitlyk, V.; Pomjakushina, E.; Puzniak, R.; Conder, K.

    2016-07-01

    Alkali metal intercalated iron selenide superconductors A x Fe2-y Se2 (where A  =  K, Rb, Cs, Tl/K, and Tl/Rb) are characterized by several unique properties, which were not revealed in other superconducting materials. The compounds crystallize in overall simple layered structure with FeSe layers intercalated with alkali metal. The structure turned out to be pretty complex as the existing Fe-vacancies order below ~550 K, which further leads to an antiferromagnetic ordering with Néel temperature fairly above room temperature. At even lower temperatures a phase separation is observed. While one of these phases stays magnetic down to the lowest temperatures the second is becoming superconducting below ~30 K. All these effects give rise to complex relationships between the structure, magnetism and superconductivity. In particular the iron vacancy ordering, linked with a long-range magnetic order and a mesoscopic phase separation, is assumed to be an intrinsic property of the system. Since the discovery of superconductivity in those compounds in 2010 they were investigated very extensively. Results of the studies conducted using a variety of experimental techniques and performed during the last five years were published in hundreds of reports. The present paper reviews scientific work concerning methods of synthesis and crystal growth, structural and superconducting properties as well as pressure investigations.

  20. Packing transition in alkali metallic clusters

    NASA Astrophysics Data System (ADS)

    Kawai, R.; Sung, Ming Wen; Weare, John H.

    1996-03-01

    Small metallic clusters form a local geometric configuration quite different from the bulk crystals. As the cluster size increases, several transitions in the local coordination take place before the bulk structure appears. These transitions involve change in the nature of chemical bonds. We have systematically investigated the structural transition of various alkali metal clusters including binary compounds using an ab initio molecular dynamics simulation. Among them, Li clusters exhibit unusual transition in their packing pattern. Small lithium clusters (N <= 21) form open structures based on a ``solvation shell''.(M. Sung, R. Kawai, and J. Weare, Phys. Rev. Lett. 73) (1994) 3552., which is quite different from other alkali metal clusters. The bonding of these small clusters is partially ionic. Above N=25, a close-packed structure is established. However, the local configuration still differ from that of the bulk crystal. As the size further increases, the ionic nature decreases and the system reaches another close-packed structure based on the Mackay icosahedron, which is similar to the bulk crystal structure.

  1. Decalcification resistance of alkali-activated slag.

    PubMed

    Komljenović, Miroslav M; Baščarević, Zvezdana; Marjanović, Nataša; Nikolić, Violeta

    2012-09-30

    This paper analyses the effects of decalcification in concentrated 6M NH(4)NO(3) solution on mechanical and microstructural properties of alkali-activated slag (AAS). Portland-slag cement (CEM II/A-S 42.5 N) was used as a benchmark material. Decalcification process led to a decrease in strength, both in AAS and in CEM II, and this effect was more pronounced in CEM II. The decrease in strength was explicitly related to the decrease in Ca/Si atomic ratio of C-S-H gel. A very low ratio of Ca/Si ~0.3 in AAS was the consequence of coexistence of C-S-H(I) gel and silica gel. During decalcification of AAS almost complete leaching of sodium and tetrahedral aluminum from C-S-H(I) gel also took place. AAS showed significantly higher resistance to decalcification in relation to the benchmark CEM II due to the absence of portlandite, high level of polymerization of silicate chains, low level of aluminum for silicon substitution in the structure of C-S-H(I), and the formation of protective layer of polymerized silica gel during decalcification process. In stabilization/solidification processes alkali-activated slag represents a more promising solution than Portland-slag cement due to significantly higher resistance to decalcification. PMID:22818592

  2. Superconductivity in alkali metal intercalated iron selenides

    NASA Astrophysics Data System (ADS)

    Krzton-Maziopa, A.; Svitlyk, V.; Pomjakushina, E.; Puzniak, R.; Conder, K.

    2016-07-01

    Alkali metal intercalated iron selenide superconductors A x Fe2‑y Se2 (where A  =  K, Rb, Cs, Tl/K, and Tl/Rb) are characterized by several unique properties, which were not revealed in other superconducting materials. The compounds crystallize in overall simple layered structure with FeSe layers intercalated with alkali metal. The structure turned out to be pretty complex as the existing Fe-vacancies order below ~550 K, which further leads to an antiferromagnetic ordering with Néel temperature fairly above room temperature. At even lower temperatures a phase separation is observed. While one of these phases stays magnetic down to the lowest temperatures the second is becoming superconducting below ~30 K. All these effects give rise to complex relationships between the structure, magnetism and superconductivity. In particular the iron vacancy ordering, linked with a long-range magnetic order and a mesoscopic phase separation, is assumed to be an intrinsic property of the system. Since the discovery of superconductivity in those compounds in 2010 they were investigated very extensively. Results of the studies conducted using a variety of experimental techniques and performed during the last five years were published in hundreds of reports. The present paper reviews scientific work concerning methods of synthesis and crystal growth, structural and superconducting properties as well as pressure investigations.

  3. Calcic myrmekite in anorthositic and gabbroic rocks

    SciTech Connect

    Schiffries, C.M.; Dymek, R.F.

    1985-01-01

    Myrmekite is a common feature of granitic plutonic rocks and quartzo-feldspathic gneisses, but it is rarely reported in anorthositic and gabbroic rocks. The authors have identified myrmekitic intergrowths of quartz and calcic plagioclase in a variety of plagioclase-rich cumulate rocks, including samples from a number of massif anorthosites and layered igneous intrusions. It appears that calcic myrmekite has been frequently overlooked, and is a common accessory feature in these rock types. Chemical and textural characteristics of myrmekite in the St-Urbain massif anorthosite (Quebec) and the Bushveld Igneous Complex (South Africa) have several features in common, but this myrmekite appears to be fundamentally different from that described by most previous investigators. Whereas myrmekite typically consists of a vermicular intergrowth of sodic plagioclase and quartz that occurs adjacent to alkali feldspar, the intergrowths in these rocks contain highly calcic plagioclase and lack the intervening alkali feldspar. In addition, the plagioclase in the myrmekite is more calcic than that in the surrounding rock. The boundary between the myrmekite and the host material is generally extremely sharp, although reverse zoning of host plagioclase may obscure the contact in some cases. The textural and chemical evidence is consistent with a replacement origin for these intergrowths; the proportion of quartz in the myrmekite is in close agreement with the predicted amount of silica that is generated by the theoretical replacement reaction. It appears that water played a key role in the replacement process.

  4. Metamorphism of San Antonio Terrane metapelites, San Gabriel Mountains, California

    SciTech Connect

    Archuleta, L.; Ishimatsu, J.; Schneiderman, J.S. . Geology Dept.)

    1993-04-01

    Pelitic schists and gneisses from the San Antonio terrane in the eastern San Gabriel Mountains consist of garnet, biotite, plagioclase, quartz, sillimanite, cordierite, hercynite [+-] alkali feldspar. Large garnet porphyroblasts contain quartz, plagioclase and sillimanite inclusions. Cordierite occurs as haloes around garnet porphyroblasts and as small subgrains always associated with hercynite and together replacing sillimanite blades. Hercynite additionally appears to have nucleated on the edges of sillimanite blades. Contrary to previous investigations, hercynite appears to be a late mineral phase. Reaction textures described above have been used to calculate a set of net-transfer reactions that can be used (1) to characterize all possible exchanges of matter between minerals in the system and (2) to construct a reaction space for the system. Fourteen thin sections with large garnet porphyroblasts and abundant biotite were used for microprobe analysis. Detailed probe analyses show well-developed zoning in the plagioclase and alkali feldspar whose character varies depending on location in the thin section relative to neighboring minerals. Generally, large plagioclase porphyroblasts display normal zoning and are not as calcium-rich as plagioclase inclusions in the garnet. Garnet porphyroblasts have flat zoning profiles due to high temperatures of metamorphism. Pressures and temperatures of metamorphism have been calculated from these assemblages using garnet-biotite geothermometry and quartz-garnet-aluminosilicate-plagioclase geobarometry.

  5. Formation of lysinoalanine in egg white under alkali treatment.

    PubMed

    Zhao, Yan; Luo, Xuying; Li, Jianke; Xu, Mingsheng; Tu, Yonggang

    2016-03-01

    To investigate the formation mechanism of lysinoalanine (LAL) in eggs during the alkali treatment process, NaOH was used for the direct alkali treatment of egg white, ovalbumin, and amino acids; in addition, the amount of LAL formed during the alkali treatment process was measured. The results showed that the alkali treatment resulted in the formation of LAL in the egg white. The LAL content increased with increasing pH and temperature, with the LAL content first increasing and then leveling off with increasing time. The amount of LAL formed in the ovalbumin under the alkali treatment condition accounted for approximately 50.51% to 58.68% of the amount of LAL formed in the egg white. Thus, the LAL formed in the ovalbumin was the main source for the LAL in the egg white during the alkali treatment process. Under the alkali treatment condition, free L-serine, L-cysteine, and L-cystine reacted with L-lysine to form LAL; therefore, they are the precursor amino acids of LAL formed in eggs during the alkali treatment process. PMID:26772660

  6. 40 CFR 721.4740 - Alkali metal nitrites.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... defined in 40 CFR 721.3) containing amines. (b) ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Alkali metal nitrites. 721.4740... Substances § 721.4740 Alkali metal nitrites. (a) Chemical substances and significant new use subject...

  7. 40 CFR 721.4740 - Alkali metal nitrites.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... defined in 40 CFR 721.3) containing amines. (b) ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Alkali metal nitrites. 721.4740... Substances § 721.4740 Alkali metal nitrites. (a) Chemical substances and significant new use subject...

  8. 40 CFR 721.4740 - Alkali metal nitrites.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... defined in 40 CFR 721.3) containing amines. (b) ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkali metal nitrites. 721.4740... Substances § 721.4740 Alkali metal nitrites. (a) Chemical substances and significant new use subject...

  9. 40 CFR 721.4740 - Alkali metal nitrites.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... defined in 40 CFR 721.3) containing amines. (b) ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alkali metal nitrites. 721.4740... Substances § 721.4740 Alkali metal nitrites. (a) Chemical substances and significant new use subject...

  10. Self-discharge in bimetallic cells containing alkali metal

    NASA Technical Reports Server (NTRS)

    Foster, M. S.; Hesson, J. C.; Shimotake, H.

    1969-01-01

    Theoretical analysis of thermally regenerative bimetallic cells with alkali metal anodes shows a relation between the current drawn and the rate of discharge under open-circuit conditions. The self-discharge rate of the cell is due to the dissolution and ionization of alkali metal atoms in the fused-salt electrolyte

  11. COMPLEX FLUORIDES OF PLUTONIUM AND AN ALKALI METAL

    DOEpatents

    Seaborg, G.T.

    1960-08-01

    A method is given for precipitating alkali metal plutonium fluorides. such as KPuF/sub 5/, KPu/sub 2/F/sub 9/, NaPuF/sub 5/, and RbPuF/sub 5/, from an aqueous plutonium(IV) solution by adding hydrogen fluoride and alkali-metal- fluoride.

  12. Recovery of alkali metal constituents from catalytic coal conversion residues

    DOEpatents

    Soung, Wen Y.

    1984-01-01

    In a coal gasification operation (32) or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles by contacting them (46, 53, 61, 69) with water or an aqueous solution to remove water-soluble alkali metal constituents and produce an aqueous solution enriched in said constituents. The aqueous solution thus produced is then contacted with carbon dioxide (63) to precipitate silicon constituents, the pH of the resultant solution is increased (81), preferably to a value in the range between about 12.5 and about 15.0, and the solution of increased pH is evaporated (84) to increase the alkali metal concentration. The concentrated aqueous solution is then recycled to the conversion process (86, 18, 17) where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst.

  13. A model that helps explain Sr-isotope disequilibrium between feldspar phenocrysts and melt in large-volume silicic magma systems

    USGS Publications Warehouse

    Duffield, W.A.; Ruiz, J.

    1998-01-01

    Feldspar phenocrysts of silicic volcanic rocks are commonly in Sr-isotopic disequilibrium with groundmass. In some cases the feldspar is more radiogenic, and in others it is less radiogenic. Several explanations have been published previously, but none of these is able to accommodate both senses of disequilibrium. We present a model by which either more- or less-radiogenic feldspar (or even both within a single eruptive unit) can originate. The model requires a magma body open to interaction with biotite- and feldspar-bearing wall rock. Magma is incrementally contaminated as wall rock melts incongruently. Biotite preferentially melts first, followed by feldspar. Such melting behavior, which is supported by both field and experimental studies, first contaminates magma with a relatively radiogenic addition, followed by a less-radiogenic addition. Feldspar phenocrysts lag behind melt (groundmass of volcanic rock) in incorporating the influx of contaminant, thus resulting in Sr-isotopic disequilibrium between the crystals and melt. The sense of disequilibrium recorded in a volcanic rock depends on when eruption quenches the contamination process. This model is testable by isotopic fingerprinting of individual feldspar crystals. For a given set of geologic boundary conditions, specific core-to-rim Sr-isotopic profiles are expectable. Moreover, phenocrysts that nucleate at different times during the contamination process should record different and predictable parts of the history. Initial results of Sr-isotopic fingerprinting of sanidine phenocrysts from the Taylor Creek Rhyolite are consistent with the model. More tests of the model are desirable.Feldspar phenocrysts of silicic volcanic rocks are commonly in Sr-isotopic disequilibrium with groundmass. In some cases the feldspar is more radiogenic, and in others it is less radiogenic. Several explanations have been published previously, but none of these is able to accommodate both senses of disequilibrium. We present a

  14. Performance of Straight Steel Fibres Reinforced Alkali Activated Concrete

    NASA Astrophysics Data System (ADS)

    Faris, Meor Ahmad; Bakri Abdullah, Mohd Mustafa Al; Nizar Ismail, Khairul; Muniandy, Ratnasamy; Putra Jaya, Ramadhansyah

    2016-06-01

    This paper focus on the performance of alkali activated concrete produced by using fly ash activated by sodium silicate and sodium hydroxide solutions. These alkali activated concrete were reinforced with straight steel fibres with different weight percentage starting from 0 % up to 5 %. Chemical composition of raw material in the production alkali activated concrete which is fly ash was first identified by using X-ray fluorescence. Results reveal there have an effect of straight steel fibres inclusion to the alkali activated concrete. Highest compressive strength of alkali activated concrete which is 67.72 MPa was obtained when 3 % of straight fibres were added. As well as flexural strength, highest flexural strength which is 6.78 MPa was obtained at 3 % of straight steel fibres inclusions.

  15. Effects of alkali treatments on Ag nanowire transparent conductive films

    NASA Astrophysics Data System (ADS)

    Kim, Sunho; Kang, Jun-gu; Eom, Tae-yil; Moon, Bongjin; Lee, Hoo-Jeong

    2016-06-01

    In this study, we employ various alkali materials (alkali metals with different base strengths, and ammonia gas and solution) to improve the conductivity of silver nanowire (Ag NW)-networked films. The alkali treatment appears to remove the surface oxide and improve the conductivity. When applied with TiO2 nanoparticles, the treatment appears more effective as the alkalis gather around wire junctions and help them weld to each other via heat emitted from the reduction reaction. The ammonia solution treatment is found to be quick and aggressive, damaging the wires severely in the case of excessive treatment. On the other hand, the ammonia gas treatment seems much less aggressive and does not damage the wires even after a long exposure. The results of this study highlight the effectiveness of the alkali treatment in improving of the conductivity of Ag NW-networked transparent conductive films.

  16. Albitization of plagioclase crystals in the Stevens sandstone (Miocene), San Joaquin Basin, California, and the Frio Formation (Oligocene), Gulf Coast, Texas. A TEM/AEM study

    SciTech Connect

    Hirt, W.G. ); Wenk, H.R. ); Boles, J.R. )

    1993-06-01

    Conventional Transmission Electron Microscopy (CTEM) and Analytical Electron Microscopy (AEM) studies of partially albitized plagioclase crystals taken from drill cores from the Stevens sandstone (Miocene), San Joaquin, California, and the Frio Formation (Oligocene), Gulf Coast, Texas, reveal that replacement of Ca-rich plagioclase cores by nearly pure albite (Ab[sub 96]-Ab[sub 100]) occurs along submicroscopic ([minus]15 nm wide) en echelon (001) and (110) cleavages. The cleavages are the result of changes in the localized stress regime created by dissolution of adjacent phases. Photomicrographs show albite-lined brittle cleavage crosscutting albitized semibrittle fractures. Such crosscutting relationships can be explained by a reduction in effective stress associated with the albitization process. On a macroscopic scale, this reduction in effective stress implies that the transition from hydrostatic to lithostatic pressure is discontinuous. 30 refs., 7 figs.

  17. Alkali oxide-tantalum oxide and alkali oxide-niobium oxide ionic conductors

    NASA Technical Reports Server (NTRS)

    Roth, R. S.; Parker, H. S.; Brower, W. S.; Minor, D.

    1974-01-01

    A search was made for new cationic conducting phases in alkali-tantalate and niobate systems. The phase equilibrium diagrams were constructed for the six binary systems Nb2O5-LiNbO3, Nb2O5-NaNbO3, Nb2O5-KNbO3, Ta2O5-NaTaO3, Ta2O5-LiTaO3, and Ta2O5-KTaO3. Various other binary and ternary systems were also examined. Pellets of nineteen phases were evaluated (by the sponsoring agency) by dielectric loss measurements. Attempts were made to grow large crystals of eight different phases. The system Ta2O5-KTaO3 contains at least three phases which showed peaks in dielectric loss vs. temperature. All three contain structures related to the tungsten bronzes with alkali ions in non-stoichiometric crystallographic positions.

  18. Towards better Greenland source attribution for IRD via Pb in feldspar and Ar-Ar in amphibole

    NASA Astrophysics Data System (ADS)

    Storey, C.; White, L.; Foster, G. L.; Bailey, I.; Allen, G. R.

    2012-12-01

    The provenance of Ice rafted debris, IRD, deposited in marine sediments has great potential to fingerprint regions of present and past iceberg calving in the coastal zones of continental margins. In particular, the growth of the Greenland Ice Sheet during the Pliocene intensification of northern hemisphere glaciation (and perhaps earlier) could be tracked by studying IRD in well-dated deep sea drill cores. However, the IRD record is only as strong as the onshore land-based record of potential sources. Two minerals common within IRD that have been used previously and that show great promise in this regard are feldspar and amphibole. Pb isotopes in feldspar record a diagnostic signature of the continental crust within distinct geologic terranes. In particular, Greenland is composed of a number of distinct terranes with proven distinct Pb isotope signatures. Ar-Ar dating of amphiboles records the thermal history of a terrane when it was metamorphosed above or cooled below c.550oC. Due to distinctive metamorphic histories within different terranes this signature is also potentially diagnostic of a particular source area. The two minerals together could be particularly powerful but only if the potential areas of calving are well-characterised. Here we present data form fluvio-glacial sediments from sites around the margins of Greenland and discuss their diagnostic characteristics. We also apply the principle to some circum-Greenland core top IRD samples and Mid Pliocene IRD from ODP Site 907.

  19. Heat pipes containing alkali metal working fluid

    NASA Technical Reports Server (NTRS)

    Morris, J. F. (Inventor)

    1981-01-01

    A technique for improving high temperature evaporation-condensation heat-transfer devices which have important and unique advantage in terrestrial and space energy processing is described. The device is in the form of a heat pipe comprising a sealed container or envelope which contains a capillary wick. The temperature of one end of the heat pipe is raised by the input of heat from an external heat source which is extremely hot and corrosive. A working fluid of a corrosive alkali metal, such as lithium, sodium, or potassium transfers this heat to a heat receiver remote from the heat source. The container and wick are fabricated from a superalloy containing a small percentage of a corrosion inhibiting or gettering element. Lanthanum, scandium, yttrium, thorium, and hafnium are utilized as the alloying metal.

  20. Volcanic Origin of Alkali Halides on Io

    NASA Technical Reports Server (NTRS)

    Schaefer, L.; Fegley, B., Jr.

    2003-01-01

    The recent observation of NaCl (gas) on Io confirms our earlier prediction that NaCl is produced volcanically. Here we extend our calculations by modeling thermochemical equilibrium of O, S, Li, Na, K, Rb, Cs, F, Cl, Br, and I as a function of temperature and pressure in a Pele-like volcanic gas with O/S/Na/Cl/K = 1.518/1/0.05/0.04/0.005 and CI chondritic ratios of the other (as yet unobserved) alkalis and halogens. For reference, the nominal temperature and pressure for Pele is 1760 plus or minus 210 K and 0.01 bars based on Galileo data and modeling.

  1. Ionic alkali halide XUV laser feasibility study

    SciTech Connect

    Yang, T.T.; Gylys, V.T.; Bower, R.D.; Harris, D.G.; Blauer, J.A.; Turner, C.E.; Hindy, R.N.

    1989-11-10

    The objective of this work is to assess the feasibility of a select set of ionic alkali halide XUV laser concepts by obtaining the relevant kinetic and spectroscopic parameters required for a proof-of-principle and conceptual design. The proposed lasers operate in the 80--200 nm spectral region and do not require input from outside radiation sources for their operation. Frequency up-conversion and frequency mixing techniques and therefore not considered in the work to be described. An experimental and theoretical study of a new type of laser operating in the extreme ultraviolet wavelength region has been conducted. The lasing species are singly ionized alkali halide molecules such as Rb{sup 2+}F{sub {minus}}, Rb{sup 2+}Br{sup {minus}} and Cs{sup 2+}F{sup {minus}}. These species are similar in electronic structure to the rare gas halide excimers, such as XeF and Krf, except that the ionic molecules emit at wavelengths of 80--200 nm, much shorter than the conventional rare-gas halide excimer laser. The radiative lifetime of these molecules are typically near 1 ns, which is about an order of magnitude shorter than that for rare-gas halide systems. The values of the cross section for stimulated emission are on the order of 1 {times} 10{sup {minus}16}cm{sup 2}. Because of the fundamental similarity to existing UV lasers, these systems show promise as a high power, efficient XUV lasers. 55 refs., 50 figs., 5 tabs.

  2. Evaluation of the Variation in Cooling Rate with Depth in the Lower Oceanic Crust at Fast-Spreading Ridges Using a Newly Developed Mg in Plagioclase Geospeedometer

    NASA Astrophysics Data System (ADS)

    Faak, K.; Chakraborty, S.; Coogan, L. A.

    2011-12-01

    The crystallization and cooling of new oceanic crust is regenerating two thirds of the Earth's surface continuously but the processes that occur during the cooling and crystallization of the magma are still poorly understood. Two end-member models have been proposed for lower crustal accretion at intermediate- to fast-spreading ridges (the "gabbro glacier" and "sheeted sill" models). These require different depth distributions of hydrothermal circulation and are likely to result in different variations of cooling rates with depth. Mapping cooling rates of samples of the lower oceanic crust as a function of depth can, therefore, allow us to distinguish between the models and constrain the thermal evolution during the generation of oceanic crust. We have developed a new geospeedometer, based on the exchange of Mg between plagioclase and clinopyroxene, to address this problem. New experiments demonstrate that the partitioning of Mg between clinopyroxene and plagioclase is strongly temperature dependent, changing by a factor of 4 between 1200°C and 900°C, such that during cooling Mg diffuses out of plagioclase into adjacent clinopyroxene grains. A finite difference diffusion model of Mg redistribution during cooling is applied to natural samples from the north wall of the Hess Deep Rift at the East Pacific Rise. 90 concentration profiles (rim - rim) from 45 crystals in 14 samples (from a depth range 0-520m below the sheeted dikes) were measured using an electron microprobe. For obtaining reliable cooling rates, Mg concentration profiles were measured along two crystallographic directions in a grain, and profiles from several crystals in one thin section are modeled. Cooling rate determinations are considered reliable only when results from all of these calculations are consistent. Fresh plagioclase crystals in coarse grained gabbros (mean grain size ~ 1mm) were chosen for the measurement of Mg contents. The shapes of these measured concentration profiles are very

  3. Complex subvolcanic magma plumbing system of an alkali basaltic maar-diatreme volcano (Elie Ness, Fife, Scotland)

    NASA Astrophysics Data System (ADS)

    Gernon, T. M.; Upton, B. G. J.; Ugra, R.; Yücel, C.; Taylor, R. N.; Elliott, H.

    2016-11-01

    Alkali basaltic diatremes such as Elie Ness (Fife, Scotland) expose a range of volcanic lithofacies that points to a complex, multi-stage emplacement history. Here, basanites contain phenocrysts including pyrope garnet and sub-calcic augites from depths of ~ 60 km. Volcanic rocks from all units, pyroclastic and hypabyssal, are characterised by rare earth element (REE) patterns that show continuous enrichment from heavy REE (HREE) to light REE (LREE), and high Zr/Y that are consistent with retention of garnet in the mantle source during melting of peridotite in a garnet lherzolite facies. Erupted garnets are euhedral and unresorbed, signifying rapid ascent through the lithosphere. The magmas also transported abundant pyroxenitic clasts, cognate with the basanite host, from shallower depths (~ 35-40 km). These clasts exhibit wide variation in texture, mode and mineralogy, consistent with growth from a range of compositionally diverse melts. Further, clinopyroxene phenocrysts from both the hypabyssal and pyroclastic units exhibit a very wide compositional range, indicative of polybaric fractionation and magma mixing. This is attributed to stalling of earlier magmas in the lower crust - principally from ~ 22 to 28 km - as indicated by pyroxene thermobarometry. Many clinopyroxenes display chemical zoning profiles, occasionally with mantles and rims of higher magnesium number (Mg#) suggesting the magmas were mobilised by juvenile basanite magma. The tuffs also contain alkali feldspar megacrysts together with Fe-clinopyroxene, zircon and related salic xenoliths, of the 'anorthoclasite suite' - inferred to have crystallised at upper mantle to lower crustal depths from salic magma in advance of the mafic host magmas. Despite evidence for entrainment of heterogeneous crystal mushes, the rapidly ascending melts experienced negligible crustal contamination. The complex association of phenocrysts, megacrysts and autoliths at Elie Ness indicates thorough mixing in a dynamic

  4. Ultrasonic coal washing to leach alkali elements from coals.

    PubMed

    Balakrishnan, S; Reddy, V Midhun; Nagarajan, R

    2015-11-01

    Deposition of fly ash particles onto heat-transfer surfaces is often one of the reasons for unscheduled shut-downs of coal-fired boilers. Fouling deposits encountered in convective sections of a boiler are characterized by arrival of ash particles in solidified (solid) state. Fouling is most frequently caused by condensation and chemical reaction of alkali vapors with the deposited ash particles creating a wet surface conducive to collect impacting ash particles. Hence, the amount of alkali elements present in coals, which, in turn, is available in the flue gas as condensable vapors, determines the formation and growth of fouling deposits. In this context, removal of alkali elements becomes vital when inferior coals having high-ash content are utilized for power generation. With the concept of reducing alkali elements present in a coal entering the combustor, whereby the fouling deposits can either be minimized or be weakened due to absence of alkali gluing effect, the ultrasonic leaching of alkali elements from coals is investigated in this study. Ultrasonic water-washing and chemical-washing, in comparison with agitation, are studied in order to estimate the intensification of the alkali removal process by sonication. PMID:26186840

  5. Alkali-activated cementitious materials: Mechanisms, microstructure and properties

    NASA Astrophysics Data System (ADS)

    Jiang, Weimin

    The goal of this study was to examine the activation reaction, microstructure, properties, identify the mechanisms of activation, and achieve an enhanced understanding of activation processes occurring during the synthesis of alkali activated cementitious materials (AAC). The discussions classify the following categories. (1) alkali activated slag cement; (2) alkali activated portland-slag cement; (3) alkali activated fly ash-slag cement; (4) alkali activated pozzolana-lime cement; (5) alkali activated pozzolana cement. The activators involved are NaOH, KOH; Nasb2SOsb4;\\ Nasb2COsb3;\\ CaSOsb4, and soluble silicate of sodium and potassium. The effect of alkali activation on the microstructure of these materials were analyzed at the micro-nanometer scale by SEM, EDS, ESEM, and TEM. Also sp{29}Si and sp{27}Al MAS-NMR, IR, Raman, TGA, and DTA were performed to characterize the phase in these systems. Slag, fly ash, silica fume, as well as blended cements containing mixtures of these and other components were characterized. A set of ordinary portland cement paste samples served as a control. This study confirmed that AAC materials have great potential because they could generate very early high strength, greater durability and high performance. Among the benefits to be derived from this research is a better understanding of the factors that control concrete properties when using AAC materials, and by controlling the chemistry and processing to produce desired microstructures and properties, as well as their durability.

  6. Controlled in-situ dissolution of an alkali metal

    DOEpatents

    Jones, Jeffrey Donald; Dooley, Kirk John; Tolman, David Donald

    2012-09-11

    A method for the controllable dissolution of one or more alkali metals from a vessel containing a one or more alkali metals and/or one or more partially passivated alkali metals. The vessel preferably comprising a sodium, NaK or other alkali metal-cooled nuclear reactor that has been used. The alkali metal, preferably sodium, potassium or a combination thereof, in the vessel is exposed to a treatment liquid, preferably an acidic liquid, more preferably citric acid. Preferably, the treatment liquid is maintained in continuous motion relative to any surface of unreacted alkali metal with which the treatment liquid is in contact. The treatment liquid is preferably pumped into the vessel containing the one or more alkali metals and the resulting fluid is extracted and optionally further processed. Preferably, the resulting off-gases are processed by an off-gas treatment system and the resulting liquids are processed by a liquid disposal system. In one preferred embodiment, an inert gas is pumped into the vessel along with the treatment liquid.

  7. Alkali elemental and potassium isotopic compositions of Semarkona chondrules

    USGS Publications Warehouse

    Alexander, C.M. O'D.; Grossman, J.N.

    2005-01-01

    We report measurements of K isotope ratios in 28 Semarkona chondrules with a wide range of petrologic types and bulk compositions as well as the compositions of CPX-mesostasis pairs in 17 type I Semarkona chondrules, including two chondrules with radial alkali zonation and 19 type II chondrules. Despite the wide range in K/Al ratios, no systematic variations in K isotopic compositions were found. Semarkona chondrules do not record a simple history of Rayleigh-type loss of K. Experimentally determined evaporation rates suggest that considerable alkali evaporation would have occurred during chondrule formation. Nevertheless, based on Na CPX-mesostasis distribution coefficients, the alkali contents of the cores of most chondrules in Semarkona were probably established at the time of final crystallization. However, Na CPX-mesostasis distribution coefficients also show that alkali zonation in type I Semarkona chondrules was produced by entry of alkalis after solidification, probably during parent body alteration. This alkali metasomatism may have gone to completion in some chondrules. Our preferred explanation for the lack of systematic isotopic enrichments, even in alkali depleted type I chondrule cores, is that they exchanged with the ambient gas as they cooled. ?? The Meteoritical Society, 2005.

  8. Crustal Assimilation and Magma Recharge in the Recent Mt. Etna Magma Plumbing System: Evidence from In Situ Plagioclase Textural and Compositional Data

    NASA Astrophysics Data System (ADS)

    Pitcher, B. W.; Bohrson, W. A.; Viccaro, M.

    2011-12-01

    Mt. Etna is Europe's largest and most active volcano, and as a result of its proximity to populated areas, understanding the structure of its magma plumbing system and the nature of its magmatic processes is essential for better predicting eruptive hazards. The aim of this study is to document core to rim textural, chemical, and isotopic variations in plagioclase, in order to investigate the physical characteristics of the subvolcanic magma system and processes by which magmas evolve. Nomarski Differential Interference Contrast (NDIC) imaging was used to characterize the complex textures of plagioclase crystals in six trachybasaltic samples from eruption years 1974, 1981, 2001, and 2004. Approximately 30 NDIC images per sample revealed 6 textural categories defined by combinations of monotonous, oscillatory, sieve, and patchy zoning. Core to rim electron microprobe analyses carried out at distinct textural boundaries revealed variable anorthite (An) (mol %) values ranging from 92 to 44. In most phenocrysts, An decreases non-monotonically from core to rim, and simple correlations among An, FeO (wt. %), textural type, and eruption year are lacking, indicating intricate crystallization histories that likely reflect changing magma chamber conditions. Laser Ablation Inductively Coupled Plasma Mass Spectrometer (LA-ICPMS) 87Sr/86Sr analyses were performed on cores and rims of selected crystals from each textural type within each sample. Phenocryst 87Sr/86Sr values ranged from ~0.70300 to 0.70370 (±.00002), and were significantly lower than preliminary groundmass 87Sr/86Sr values, which ranged from ~0.70466 to 0.70498. Whole-rock 87Sr/86Sr values are between groundmass and crystal values. The Δ87Sr/86Sr within each crystal, defined as rim minus core, varied from -0.00030 to +0.00011; while most crystals exhibit a core to rim increase, some showed a decrease and some had constant 87Sr/86Sr. The prevalence of core to rim increases, combined with whole rock and preliminary

  9. Electrochemical cell utilizing molten alkali metal electrode-reactant

    DOEpatents

    Virkar, Anil V.; Miller, Gerald R.

    1983-11-04

    An improved electrochemical cell comprising an additive-modified molten alkali metal electrode-reactant and/or electrolyte is disclosed. Various electrochemical cells employing a molten alkali metal, e.g., sodium, electrode in contact with a cationically conductive ceramic membrane experience a lower resistance and a lower temperature coefficient of resistance whenever small amounts of selenium are present at the interface of the electrolyte and the molten alkali metal. Further, cells having small amounts of selenium present at the electrolyte-molten metal interface exhibit less degradation of the electrolyte under long term cycling conditions.

  10. Bilayer resist system utilizing alkali-developable organosilicon positive photoresist

    NASA Astrophysics Data System (ADS)

    Nate, Kazuo; Mizushima, Akiko; Sugiyama, Hisashi

    1991-06-01

    A bi-layer resist system utilizing an alkali-developable organosilicon positive photoresist (OSPR) has been developed. The composite prepared from an alkali-soluble organosilicon polymer, poly(p- hydroxybenzylsilsesquioxane) and naphthoquinone diazide becomes a alkali-developable positive photoresist which is sensitive to UV (i line - g line) region, and exhibited high oxygen reactive ion etching (O2 RIE) resistance. The sensitivity and the resolution of OSPR are almost the same as those of conventional novolac-based positive photoresists. The bi-layer resist system utilizing OSPR as the top imaging layer gave fine patterns of underlayers with high aspect ratio easily.

  11. High temperature alkali corrosion of ceramics in coal gas

    SciTech Connect

    Pickrell, G.R.; Sun, T.; Brown, J.J.

    1992-02-24

    The high temperature alkali corrosion kinetics of SiC have been systematically investigated from 950 to 1100[degrees]C at 0.63 vol % alkali vapor concentration. The corrosion rate in the presence of alkaliis approximately 10[sup 4] to 10[sup 5] times faster than the oxidation rate of SiC in air. The activation energy associated with the alkali corrosion is 406 kJ/mol, indicating a highly temperature-dependent reaction rate. The rate-controlling step of the overall reaction is likely to be the dissolution of silica in the sodium silicate liquid, based on the oxygen diffusivity data.

  12. Increasing Class C fly ash reduces alkali silica reactivity

    SciTech Connect

    Hicks, J.K.

    2007-07-01

    Contrary to earlier studies, it has been found that incremental additions of Class C fly ash do reduce alkali silica reactivity (ASR), in highly reactive, high alkali concrete mixes. AST can be further reduced by substituting 5% metakaolin or silica fume for the aggregate in concrete mixes with high (more than 30%) Class C fly ash substitution. The paper reports results of studies using Class C fly ash from the Labadie Station plant in Missouri which typically has between 1.3 and 1.45% available alkalis by ASTM C311. 7 figs.

  13. Hydrothermal alteration and mass exchange in the hornblende latite porphyry, Rico, Colorado

    NASA Astrophysics Data System (ADS)

    Larson, Peter B.; Cunningham, Charles G.; Naeser, Charles W.

    1994-03-01

    The Rico paleothermal anomaly, southwestern Colorado, records the effects of a large hydrothermal system that was active at 4 Ma. This hydrothermal system produced the deep Silver Creek stockwork Mo deposit, which formed above the anomaly's heat source, and shallower base and precious-metal vein and replacement deposits. A 65 Ma hornblende latite porphyry is present as widespread sills throughout the area and provided a homogenous material that recorded the effects of the hydrothermal system up to 8 km from the center. Hydrothermal alteration in the latite can be divided into a proximal facies which consists of two assemblages, quartz-illite-calcite and chlorite-epidote, and a distal facies which consists of a distinct propylitic assemblage. Temperatures were gradational vertically and laterally in the anomaly, and decreased away from the centra heat source. A convective hydrothermal plume, 3 km wide and at least 2 km high, was present above the stock-work molybdenum deposit and consisted of upwelling, high-temperature fluids that produced the proximal alteration facies. Distal facies alteration was produced by shallower cooler fluids. The most important shallow base and precious-metal vein deposits in the Rico district are at or close to the boundary of the thermal plume. Latite within the plume had a large loss of Na2O, large addition of CaO, and variable SiO2 exchante. Distal propylitized latite samples lost small amounts of Na2O and CaO and exchanged minor variable amounts of SiO2. The edge of the plume is marked by steep Na2O exchange gradients. Na2O exchange throughout the paleothermal anomaly was controlled by the reaction of the albite components in primary plagioclase and alkali feldspars. Initial feldspar alteration in the distal facies was dominated by reaction of the plagioclase, and the initial molar ratio of reactants (alkali feldspar albite component to plagioclase albite component) was 0.35. This ratio of the moles of plagioclase to alkali feldspar

  14. Electric field-induced softening of alkali silicate glasses

    SciTech Connect

    McLaren, C.; Heffner, W.; Jain, H.; Tessarollo, R.; Raj, R.

    2015-11-02

    Motivated by the advantages of two-electrode flash sintering over normal sintering, we have investigated the effect of an external electric field on the viscosity of glass. The results show remarkable electric field-induced softening (EFIS), as application of DC field significantly lowers the softening temperature of glass. To establish the origin of EFIS, the effect is compared for single vs. mixed-alkali silicate glasses with fixed mole percentage of the alkali ions such that the mobility of alkali ions is greatly reduced while the basic network structure does not change much. The sodium silicate and lithium-sodium mixed alkali silicate glasses were tested mechanically in situ under compression in external electric field ranging from 0 to 250 V/cm in specially designed equipment. A comparison of data for different compositions indicates a complex mechanical response, which is observed as field-induced viscous flow due to a combination of Joule heating, electrolysis and dielectric breakdown.

  15. Method for intercalating alkali metal ions into carbon electrodes

    DOEpatents

    Doeff, M.M.; Ma, Y.; Visco, S.J.; DeJonghe, L.

    1995-08-22

    A low cost, relatively flexible, carbon electrode for use in a secondary battery is described. A method is provided for producing same, including intercalating alkali metal salts such as sodium and lithium into carbon.

  16. Alkali activation of halloysite for adsorption and release of ofloxacin

    NASA Astrophysics Data System (ADS)

    Wang, Qin; Zhang, Junping; Wang, Aiqin

    2013-12-01

    Halloysite nanotubes are promising vehicles for the controlled release of drug molecules. Here, we systematically investigated the effects of alkali activation on the physicochemical properties, structure and morphology of halloysite nanotubes by XRD, FTIR, SEM and TEM, etc. Afterwards, the adsorption and in vitro release properties of halloysite for cationic ofloxacin (OFL) were evaluated. The results indicate that alkali activation dissolves amorphous aluminosilicate, free silica and alumina, which results in the increase in pore volume and pore size. OFL is adsorbed onto halloysite via electrostatic interaction and complexation. Alkali activation could increase the adsorption capacity of halloysite for OFL and prolong release of the adsorbed OFL compared with the natural halloysite. Thus, alkali activation of halloysite is an effective protocol to improve the adsorption and prolong release for cationic drug molecules.

  17. Hall Determination of Atomic Radii of Alkali Metals

    ERIC Educational Resources Information Center

    Houari, Ahmed

    2008-01-01

    I will propose here an alternative method for determining atomic radii of alkali metals based on the Hall measurements of their free electron densities and the knowledge of their crystal structure. (Contains 2 figures.)

  18. Effect of cavitation on removal of alkali elements from coal

    NASA Astrophysics Data System (ADS)

    Srivalli, H.; Nirmal, L.; Nagarajan, R.

    2015-12-01

    The main impurities in coal are sulphur, ash and alkali. On combustion, the volatile forms of these impurities are either condensed on the boilers, or emitted in the form of potentially hazardous gases. The alkali elements present in coal help the fly ash particles adhere to boiler surfaces by providing a wet surface on which collection of these particles can take place. Use of ultrasonic techniques in cleaning of coal has stirred interest among researchers in recent times. Extraction of alkali elements by cavitation effect using low-frequency ultrasound, in the presence of reagents (HNO3 and H2O2) is reported in this paper. Powdered coal was dissolved with the reagent and exposed to ultrasonic fields of various frequencies at different time intervals. The treated solution is filtered and tested for alkali levels.

  19. The 4843 Alkali Metal Storage Facility Closure Plan

    SciTech Connect

    Not Available

    1991-06-01

    The 4843 AMSF has been used primarily to provide a centralized building to receive and store dangerous and mixed alkali metal waste, including sodium and lithium, which has been generated at the Fast Flux Test Facility and at various other Hanford Site operations that used alkali metals. Most of the dangerous and mixed alkali metal waste received consists of retired equipment from liquid sodium processes. The unit continues to store material. In general, only solid alkali metal waste that is water reactive is stored at the 4843 AMSF. The 4843 AMSF will be closed in a manner consistent with Ecology guidelines and regulations (WAC 173-303-610). The general closure procedure is detailed as follows.

  20. Method for intercalating alkali metal ions into carbon electrodes

    DOEpatents

    Doeff, Marca M.; Ma, Yanping; Visco, Steven J.; DeJonghe, Lutgard

    1995-01-01

    A low cost, relatively flexible, carbon electrode for use in a secondary battery is described. A method is provided for producing same, including intercalating alkali metal salts such as sodium and lithium into carbon.

  1. Alkali absorption and citrate excretion in calcium nephrolithiasis

    NASA Technical Reports Server (NTRS)

    Sakhaee, K.; Williams, R. H.; Oh, M. S.; Padalino, P.; Adams-Huet, B.; Whitson, P.; Pak, C. Y.

    1993-01-01

    The role of net gastrointestinal (GI) alkali absorption in the development of hypocitraturia was investigated. The net GI absorption of alkali was estimated from the difference between simple urinary cations (Ca, Mg, Na, and K) and anions (Cl and P). In 131 normal subjects, the 24 h urinary citrate was positively correlated with the net GI absorption of alkali (r = 0.49, p < 0.001). In 11 patients with distal renal tubular acidosis (RTA), urinary citrate excretion was subnormal relative to net GI alkali absorption, with data from most patients residing outside the 95% confidence ellipse described for normal subjects. However, the normal relationship between urinary citrate and net absorbed alkali was maintained in 11 patients with chronic diarrheal syndrome (CDS) and in 124 stone-forming patients devoid of RTA or CDS, half of whom had "idiopathic" hypocitraturia. The 18 stone-forming patients without RTA or CDS received potassium citrate (30-60 mEq/day). Both urinary citrate and net GI alkali absorption increased, yielding a significantly positive correlation (r = 0.62, p < 0.0001), with the slope indistinguishable from that of normal subjects. Thus, urinary citrate was normally dependent on the net GI absorption of alkali. This dependence was less marked in RTA, confirming the renal origin of hypocitraturia. However, the normal dependence was maintained in CDS and in idiopathic hypocitraturia, suggesting that reduced citrate excretion was largely dietary in origin as a result of low net alkali absorption (from a probable relative deficiency of vegetables and fruits or a relative excess of animal proteins).

  2. Electrochemical cell having an alkali-metal-nitrate electrode

    DOEpatents

    Roche, M.F.; Preto, S.K.

    1982-06-04

    A power-producing secondary electrochemical cell includes a molten alkali metal as the negative-electrode material and a molten-nitrate salt as the positive-electrode material. The molten material in the respective electrodes are separated by a solid barrier of alkali-metal-ion conducting material. A typical cell includes active materials of molten sodium separated from molten sodium nitrate and other nitrates in mixture by a layer of sodium ..beta..'' alumina.

  3. Alkali metal yttrium neo-pentoxide double alkoxide precursors to alkali metal yttrium oxide nanomaterials

    DOE PAGES

    Boyle, Timothy J.; Neville, Michael L.; Sears, Jeremiah Matthew; Cramer, Roger

    2016-03-15

    In this study, a series of alkali metal yttrium neo-pentoxide ([AY(ONep)4]) compounds were developed as precursors to alkali yttrium oxide (AYO2) nanomaterials. The reaction of yttrium amide ([Y(NR2)3] where R=Si(CH3)3) with four equivalents of H-ONep followed by addition of [A(NR2)] (A=Li, Na, K) or Ao (Ao=Rb, Cs) led to the formation of a complex series of AnY(ONep)3+n species, crystallographically identified as [Y2Li3(μ3-ONep)(μ3-HONep)(μ-ONep)5(ONep)3(HONep)2] (1), [YNa2(μ3-ONep)4(ONep)]2 (2), {[Y2K3(μ3-ONep)3(μ-ONep)4(ONep)2(ηξ-tol)2][Y4K2(μ4-O)(μ3-ONep)8(ONep)4]•ηx-tol]} (3), [Y4K2(μ4-O)(μ3-ONep)8(ONep)4] (3a), [Y2Rb3(μ4-ONep)3(μ-ONep)6] (4), and [Y2Cs4(μ6-O)(μ3-ONep)6(μ3-HONep)2(ONep)2(ηx-tol)4]•tol (5). Compounds 1–5 were investigated as single source precursors to AYOx nanomaterials following solvothermal routes (pyridine, 185 °C for 24h). The final products after thermal processing weremore » found by powder X-ray diffraction experiments to be Y2O3 with variable sized particles based on transmission electron diffraction. Energy dispersive X-ray spectroscopy studies indicated that the heavier alkali metal species were present in the isolated nanomaterials.« less

  4. Analysis of Silicate Melt Inclusions in Plagioclase Phenocrysts in Prehistoric Tephra ˜1400 Years B.P. From Augustine Volcano, Alaska.

    NASA Astrophysics Data System (ADS)

    Tappen, C. M.; Webster, J. D.; Mandeville, C. W.

    2003-12-01

    Augustine volcano, located in southern Cook Inlet, Alaska, has been historically active, erupting 6 times in the last 200 years. Eruptions first began prior to 40,000 years B.P. (Begét and Kienle, 1992). There are a minimum of 6 prehistoric tephra layers, G (oldest), I, H, C, M and B (youngest), present on Augustine Island (Waitt et al, 1996). In this study, we analyzed glassy silicate melt inclusions in plagioclase phenocrysts from tephra layer H ( ˜1400 years B.P.) for major and minor and some trace elements (Cl, F, S, Ba, and Sr) by electron microprobe. We use the data to determine the chemical variation of melt inclusions in specific locations within zoned plagioclase phenocrysts. Plagioclase phenocrysts (0.5 to 4 mm long) exhibit unzoned, oscillatory or patchy zoned regions. Unzoned phenocryst cores lack melt inclusions. Patchy zonation occurs in cores and is sometimes found in intermediate zones between the core and rim. Planar oscillatory zones are distinguished in BSE images by light (An56-90) and dark (An46-55) bands. In some phenocrysts light and dark layers differ only by 1% An. Most phenocrysts show 2-3 repeated oscillating pairs of light and dark plagioclase compositional layers. Normal and reverse zoning are apparent in phenocrysts. Rims tend to be more calcic than the cores, varying from 1-5% An. Large melt inclusions (60 to 70 μ m long) are located in patchy zoned cores. Small melt inclusions (2 to 10 μ m long) are located at the contact of high calcic and low calcic oscillatory layers. All melt inclusions are trapped along compositional boundaries and occur in the more calcic plagioclase. Petrography suggests that melt inclusions may have been formed by partial dissolution of a less calcic plagioclase layer. The composition of the melt inclusions are rhyolitic (71 to 75% SiO2). The chlorine concentrations range from 3020 to 6100 ppm with the more chlorine enriched concentrations occurring in the outer rims of the phenocryst. Sr and Ba vary from

  5. Compositional Characteristics of Plagioclase Crystal Size Distributions (CSDs) from the 2000 B.P. Eruption of El Misti Volcano, Southern Peru

    NASA Astrophysics Data System (ADS)

    Marshall, L. X.; Tepley, F. J.; de Silva, S. L.

    2011-12-01

    The most recent significant explosive eruption of El Misti in southern Peru occurred 2000 yr B.P., producing considerable pyroclastic deposits and extensive lahars. Juvenile blocks from the 2000 B.P. eruption reveal the mixing of two magmas: a plagioclase rhyolite and amphibole-plagioclase andesite (Tepley et al., 2011). Plagioclase phenocrysts, microphenocrysts and microlites in both magmas have a wide compositional range, but can be organized based on composition: a Low-An group (An60-35) that grew from the rhyolitic magma and a High-An group (An88-65) that grew from the andesitic magma. To better understand the evolution of these magmas and the exchange of material during mixing, crystal size distributions (CSDs) of plagioclase were determined on five samples across the compositional spectrum to assess and quantify both the mixing relationship and cooling history of each magma. For all samples, CSDs were determined via high-resolution Al Kα x-ray maps, and were collected on a large (35 mm x 20 mm) and small scale (3 mm x 3 mm) to allow for measurement of a large range of crystal sizes. Individual crystals were outlined and processed through ImageJ, and crystal distributions were determined through CSDCorrections (v. 1.39; Higgins, 2000). Crystal aspect ratios of plagioclase were determined through CSDSlice5 (Morgan and Jerram, 2006), a method of inverting 2D data (short axis/long axis) into 3D volumetric data. CSDs for each sample are defined by two distinct slopes (shallow and steep) with a pronounced change in slope at ~0.3 mm crystal length. CSD slopes for phenocrysts (crystals >0.3 mm) are shallow with low intercepts, reflecting low nucleation rates and low degrees of undercooling. In comparison, CSD slopes for microphenocrysts and microlites (<0.3 mm) are steep with high intercepts, and these patterns may reflect both higher nucleation rates and cooling rates than for the phenocrysts. Kinked CSDs are commonly associated with magma mixing, based on the

  6. Reduction of phosphorus and alkali levels in coking coals

    SciTech Connect

    Hoare, I.C.; Waugh, A.B.

    1995-12-31

    A number of coals, though exhibiting desirable coking properties, can have undesirable levels of alkalis and phosphorus. All the phosphorus in the coal will report to the coke, eventually to the iron and thence to the steel, with adverse effects on its metallurgical properties. Alkalis have damaging effects on the blast furnace operation and can be responsible for loss of heat, loss of production, efficiency loss and reduced furnace life. Buyers of coking coal commonly specify such parameters as phosphorus in coal and alkalis in ash, with penalties and rejection over certain limits. With the introduction of new direct reduction technologies such as COREX and HISMELT, and others such as PCI, it is anticipated that coal producers will have even tighter phosphorus and alkali specifications imposed on their products. Phosphorus is predominantly inorganic in origin occurring in a wide variety of minerals in coal, but its main source is apatite. It can be found mainly in the lower density fractions of the coal and intimately bound, so that conventional physical beneficiation techniques are relatively ineffective. CSIRO has developed a cost effective, selective chemical demineralization treatment, which can be applied to the problem of high alkali, high phosphorus coals. This particular technique makes use of unrefined organic acid, which also has the advantage of being low in cost and environmentally benign. In this paper, the effectiveness of acid demineralization of a number of coals is discussed, within the context of their phosphorus and alkali distributions throughout various size/density fractions.

  7. Two-phase alkali-metal experiments in reduced gravity

    SciTech Connect

    Antoniak, Z.I.

    1986-06-01

    Future space missions envision the use of large nuclear reactors utilizing either a single or a two-phase alkali-metal working fluid. The design and analysis of such reactors require state-of-the-art computer codes that can properly treat alkali-metal flow and heat transfer in a reduced-gravity environment. A literature search of relevant experiments in reduced gravity is reported on here, and reveals a paucity of data for such correlations. The few ongoing experiments in reduced gravity are noted. General plans are put forth for the reduced-gravity experiments which will have to be performed, at NASA facilities, with benign fluids. A similar situation exists regarding two-phase alkali-metal flow and heat transfer, even in normal gravity. Existing data are conflicting and indequate for the task of modeling a space reactor using a two-phase alkali-metal coolant. The major features of past experiments are described here. Data from the reduced-gravity experiments with innocuous fluids are to be combined with normal gravity data from the two-phase alkali-metal experiments. Analyses undertaken here give every expectation that the correlations developed from this data base will provide a valid representation of alkali-metal heat transfer and pressure drop in reduced gravity.

  8. Bioinorganic Chemistry of the Alkali Metal Ions.

    PubMed

    Kim, Youngsam; Nguyen, Thuy-Tien T; Churchill, David G

    2016-01-01

    The common Group 1 alkali metals are indeed ubiquitous on earth, in the oceans and in biological systems. In this introductory chapter, concepts involving aqueous chemistry and aspects of general coordination chemistry and oxygen atom donor chemistry are introduced. Also, there are nuclear isotopes of importance. A general discussion of Group 1 begins from the prevalence of the ions, and from a comparison of their ionic radii and ionization energies. While oxygen and water molecule binding have the most relevance to biology and in forming a detailed understanding between the elements, there is a wide range of basic chemistry that is potentially important, especially with respect to biological chelation and synthetic multi-dentate ligand design. The elements are widely distributed in life forms, in the terrestrial environment and in the oceans. The details about the workings in animal, as well as plant life are presented in this volume. Important biometallic aspects of human health and medicine are introduced as well. Seeing as the elements are widely present in biology, various particular endogenous molecules and enzymatic systems can be studied. Sodium and potassium are by far the most important and central elements for consideration. Aspects of lithium, rubidium, cesium and francium chemistry are also included; they help in making important comparisons related to the coordination chemistry of Na(+) and K(+). Physical methods are also introduced. PMID:26860297

  9. Superconductivity in alkali-doped fullerene nanowhiskers.

    PubMed

    Takeya, Hiroyuki; Konno, Toshio; Hirata, Chika; Wakahara, Takatsugu; Miyazawa, Kun'ichi; Yamaguchi, Takahide; Tanaka, Masashi; Takano, Yoshihiko

    2016-09-01

    Superconductivity in alkali metal-doped fullerene nanowhiskers (C60NWs) was observed in K3.3C60NWs, Rb3.0C60NWs and Cs2.0Rb1.0C60NWs with transition temperatures at 17, 25 and 26 K, respectively. Almost full shielding volume fraction (~80%) was observed in K3.3C60NWs when subjected to thermal treatment at 200 °C for a duration of 24 h. In contrast, the shielding fraction of Rb3.0C60NWs and Cs2.0Rb1.0C60NWs were calculated to be 8% and 6%, respectively. Here we report on an extensive investigation of the superconducting properties of these AC60NWs (A  =  K3.3, Rb3.0 and Cs2.0Rb1.0). These properties are compared to the ones reported on the corresponding conventional (single-crystal or powder) K-doped fullerene. We also evaluated the critical current densities of these C60NWs using the Bean model under an applied magnetic field up to 50 kOe. PMID:27385220

  10. Superconductivity in alkali-doped fullerene nanowhiskers.

    PubMed

    Takeya, Hiroyuki; Konno, Toshio; Hirata, Chika; Wakahara, Takatsugu; Miyazawa, Kun'ichi; Yamaguchi, Takahide; Tanaka, Masashi; Takano, Yoshihiko

    2016-09-01

    Superconductivity in alkali metal-doped fullerene nanowhiskers (C60NWs) was observed in K3.3C60NWs, Rb3.0C60NWs and Cs2.0Rb1.0C60NWs with transition temperatures at 17, 25 and 26 K, respectively. Almost full shielding volume fraction (~80%) was observed in K3.3C60NWs when subjected to thermal treatment at 200 °C for a duration of 24 h. In contrast, the shielding fraction of Rb3.0C60NWs and Cs2.0Rb1.0C60NWs were calculated to be 8% and 6%, respectively. Here we report on an extensive investigation of the superconducting properties of these AC60NWs (A  =  K3.3, Rb3.0 and Cs2.0Rb1.0). These properties are compared to the ones reported on the corresponding conventional (single-crystal or powder) K-doped fullerene. We also evaluated the critical current densities of these C60NWs using the Bean model under an applied magnetic field up to 50 kOe.

  11. Bioinorganic Chemistry of the Alkali Metal Ions.

    PubMed

    Kim, Youngsam; Nguyen, Thuy-Tien T; Churchill, David G

    2016-01-01

    The common Group 1 alkali metals are indeed ubiquitous on earth, in the oceans and in biological systems. In this introductory chapter, concepts involving aqueous chemistry and aspects of general coordination chemistry and oxygen atom donor chemistry are introduced. Also, there are nuclear isotopes of importance. A general discussion of Group 1 begins from the prevalence of the ions, and from a comparison of their ionic radii and ionization energies. While oxygen and water molecule binding have the most relevance to biology and in forming a detailed understanding between the elements, there is a wide range of basic chemistry that is potentially important, especially with respect to biological chelation and synthetic multi-dentate ligand design. The elements are widely distributed in life forms, in the terrestrial environment and in the oceans. The details about the workings in animal, as well as plant life are presented in this volume. Important biometallic aspects of human health and medicine are introduced as well. Seeing as the elements are widely present in biology, various particular endogenous molecules and enzymatic systems can be studied. Sodium and potassium are by far the most important and central elements for consideration. Aspects of lithium, rubidium, cesium and francium chemistry are also included; they help in making important comparisons related to the coordination chemistry of Na(+) and K(+). Physical methods are also introduced.

  12. Superconductivity in alkali-doped fullerene nanowhiskers

    NASA Astrophysics Data System (ADS)

    Takeya, Hiroyuki; Konno, Toshio; Hirata, Chika; Wakahara, Takatsugu; Miyazawa, Kun'ichi; Yamaguchi, Takahide; Tanaka, Masashi; Takano, Yoshihiko

    2016-09-01

    Superconductivity in alkali metal-doped fullerene nanowhiskers (C60NWs) was observed in K3.3C60NWs, Rb3.0C60NWs and Cs2.0Rb1.0C60NWs with transition temperatures at 17, 25 and 26 K, respectively. Almost full shielding volume fraction (~80%) was observed in K3.3C60NWs when subjected to thermal treatment at 200 °C for a duration of 24 h. In contrast, the shielding fraction of Rb3.0C60NWs and Cs2.0Rb1.0C60NWs were calculated to be 8% and 6%, respectively. Here we report on an extensive investigation of the superconducting properties of these AC60NWs (A  =  K3.3, Rb3.0 and Cs2.0Rb1.0). These properties are compared to the ones reported on the corresponding conventional (single-crystal or powder) K-doped fullerene. We also evaluated the critical current densities of these C60NWs using the Bean model under an applied magnetic field up to 50 kOe.

  13. Non-Newtonian behavior of plagioclase-bearing basaltic magma: Subliquidus viscosity measurement of the 1707 basalt of Fuji volcano, Japan

    NASA Astrophysics Data System (ADS)

    Ishibashi, Hidemi

    2009-03-01

    Laboratory measurements of viscosity were done for basalt erupted in 1707 AD from Fuji volcano, Japan, using a concentric cylinder rotational viscometer at temperatures of 1297-1157 °C, 1 atm pressure, and fO 2 near the Ni-NiO buffer. On cooling, elongated plagioclase crystals with a mean length/width ratio of ca. 8.5 appeared at 1237 °C, followed by olivine at 1157 °C. At progressively lower temperatures, the total crystal volume fraction increased monotonously to ca. 0.25; viscosity increased from 38.9 to 765 Pa s at a shear strain rate of 1 s - 1 . This basalt magma behaves as a Newtonian fluid at temperatures greater than 1217 °C, but shear-thinning behavior occurs at temperatures less than 1197 °C because of the suspended plagioclase crystals. This behavior is well approximated as a power law fluid. At the onset of shear thinning, the crystal volume fraction was between 0.06 and 0.13, which is attributed to the pronounced lath-shape of plagioclase crystals. The relative viscosity increases monotonously with increase of crystal volume fraction at a constant shear strain rate, and with decrease of shear strain rate at a constant crystal volume fraction. A modified form of the Krieger-Dougherty equation is introduced herein. It enables us to describe the dependencies of relative viscosity on both the crystal volume fraction and shear strain rate, and consequently the onset of shear-thinning behavior.

  14. A mechanistic understanding of plagioclase dissolution based on Al occupancy and T-O bond length: from geologic carbon sequestration to ambient conditions.

    PubMed

    Yang, Yi; Min, Yujia; Jun, Young-Shin

    2013-11-14

    A quantitative description of how the bulk properties of aluminosilicates affect their dissolution kinetics is important in helping people understand the regulation of atmospheric CO2 concentration by silicate weathering and predict the fate and transport of geologically sequestered CO2 through brine-rock interactions. In this study, we employed a structure model based on the C1 space group to illustrate how differences in crystallographic properties of aluminosilicates, such as T-O (Tetrahedral site-Oxygen) bond length and Al/Si ordering, can result in quantifiable variations in mineral dissolution rates. The dissolution rates of plagioclases were measured under representative geologic carbon sequestration (GCS) conditions (90 °C, 100 atm of CO2, 1.0 M NaCl, and pH ∼ 3.1), and used to validate the model. We found that the logarithm of the characteristic time of the breakdown of Al-O-Si linkages in plagioclases follows a good linear relation with the mineral's aluminum content (nAl). The Si release rates of plagioclases can be calculated based on an assumption of dissolution congruency or on the regularity of Al/Si distribution in the constituent tetrahedra of the mineral. We further extended the application of our approach to scenarios where dissolution incongruency arises because of different linkage reactivities in the solid matrix, and compared the model predictions with published data. The application of our results enables a significant reduction of experimental work for determining the dissolution rates of structurally related aluminosilicates, given a reaction environment.

  15. Relation between the electroforming voltage in alkali halide-polymer diodes and the bandgap of the alkali halide

    SciTech Connect

    Bory, Benjamin F.; Wang, Jingxin; Janssen, René A. J.; Meskers, Stefan C. J.; Gomes, Henrique L.; De Leeuw, Dago M.

    2014-12-08

    Electroforming of indium-tin-oxide/alkali halide/poly(spirofluorene)/Ba/Al diodes has been investigated by bias dependent reflectivity measurements. The threshold voltages for electrocoloration and electroforming are independent of layer thickness and correlate with the bandgap of the alkali halide. We argue that the origin is voltage induced defect formation. Frenkel defect pairs are formed by electron–hole recombination in the alkali halide. This self-accelerating process mitigates injection barriers. The dynamic junction formation is compared to that of a light emitting electrochemical cell. A critical defect density for electroforming is 10{sup 25}/m{sup 3}. The electroformed alkali halide layer can be considered as a highly doped semiconductor with metallic transport characteristics.

  16. Efficient destruction of CF4 through in situ generation of alkali metals from heated alkali halide reducing mixtures.

    PubMed

    Lee, Myung Churl; Choi, Wonyong

    2002-03-15

    Perfluorocarbons (PFCs) are the most potent green house gases that are very recalcitrant at destruction. An effective way of converting PFCs using hot solid reagents into safe products has been recently introduced. By investigating the thermal reductive destruction of tetrafluoromethane (CF4) we provided new insight and more physicochemical consideration on this novel process. The complete destruction of CF4was successfully achieved by flowing the gas through a heated reagent bed (400-950 degrees C) that contained powder mixtures of alkali halides, CaO, and Si. The silicon acted as a reducing agent of alkali halides for the in-situ production of alkali metals, and the calcium oxide played the role of a halide ion acceptor. The absence of any single component in this ternary mixture drastically reduced the destruction efficiency of CF4. The CF4 destruction efficiencies with the solid reagent containing the alkali halide, MX, increased in the order of Li approximately Na < K < Cs for alkali cations and I < Br < Cl < F for halide anions. This trend agreed with the endothermicity of the alkali metal generation reaction: the higher the endothermicity, the lower the destruction efficiency. Alkali metal generation was indirectly detected by monitoring H2 production from its reaction with water. The production of alkali metals increased with NaF, KF, and CsF in this order. The CsF/CaO/Si system exhibited the complete destruction of CF4 at as low as 600 degrees C. The solid product analysis by X-ray diffraction (XRD) showed the formation of CaF2 and the depletion of Si with black carbon particles formed in the solid reagent residue. No CO/CO2 and toxic HF and SiF4 formation were detected in the exhaust gas.

  17. Alkali-aggregate reactivity of typical siliceious glass and carbonate rocks in alkali-activated fly ash based geopolymers

    NASA Astrophysics Data System (ADS)

    Lu, Duyou; Liu, Yongdao; Zheng, Yanzeng; Xu, Zhongzi; Shen, Xiaodong

    2013-08-01

    For exploring the behaviour of alkali-aggregate reactivity (AAR) in alkali-activated geopolymeric materials and assessing the procedures for testing AAR in geopolymers, the expansion behaviour of fly ash based geopolymer mortars with pure silica glass and typical carbonate rocks were studied respectively by curing at various conditions, i.e. 23°C and 38°C with relative humidity over 95%, immersed in 1M NaOH solution at 80°C. Results show that, at various curing conditions, neither harmful ASR nor harmful ACR was observed in geopolymers with the criteria specified for OPC system. However, with the change of curing conditions, the geopolymer binder and reactive aggregates may experience different reaction processes leading to quite different dimensional changes, especially with additional alkalis and elevated temperatures. It suggests that high temperature with additional alkali for accelerating AAR in traditional OPC system may not appropriate for assessing the alkali-aggregate reactivity behaviour in geopolymers designed for normal conditions. On the other hand, it is hopeful to control the dimensional change of geopolymer mortar or concrete by selecting the type of aggregates and the appropriate curing conditions, thus changing the harmful AAR in OPC into beneficial AAR in geopolymers and other alkali-activated cementitious systems.

  18. Mixed alkali effect on the spectroscopic properties of alkali-alkaline earth oxide borate glasses

    NASA Astrophysics Data System (ADS)

    Srinivas, G.; Ramesh, B.; Shareefuddin, Md.; Chary, M. N.; Sayanna, R.

    2016-05-01

    The mixed alkali and alkaline earth oxide borate glass with the composition xK2O - (25-x) Li2O-12.5BaO-12.5MgO-50B2O3 (x = 0, 5, 10, 15, 20 and 25mol %) and doped with 1mol% CuO were prepared by the melt quenching technique. From the optical absorption spectra the optical band gap, electronic polarizability(α02-), interaction parameter (A), theoretical and experimental optical basicity (Λ) values were evaluated. From the Electron Paramagnetic Resonance (EPR) spectral data the number of spins (N) and susceptibility (χ) were evaluated. The values of (α02-), and (Λ) increases with increasing of K2O content and electronic polarizability and interaction parameter show opposite behaviuor which may be due to the creation of non-bridging oxygens and expansion of borate network. The reciprocal of susceptibility (1/χ) and spin concentration (N) as a function of K2O content, varied nonlinearly which may be due to creation of non-bridging oxygens in the present glass system. This may be attributed to mixed alkali effect (MAE).

  19. Microstructural records of multiple retrograde local H2O supplement in the pelitic gneiss, Lützow-Holm Complex at Akarui Point, East Antarctica

    NASA Astrophysics Data System (ADS)

    Nakamura, Aya; Kitamura, Masao; Kawakami, Tetsuo

    2014-04-01

    The alkali-feldspar and biotite in the sillimanite-biotite-garnet gneiss from East Antarctica preserves characteristic microstructural evidence of multi-stage H2O supplement during the retrograde metamorphism. The first microstructural evidence is the "zoned feldspar," in which the mesoperthitic zone, the anti-perthitic zone, and lamella-free plagioclase zone coexist within a single crystal. They are occasionally found next to biotite, and are always depleted in orthoclase (Or) component toward the biotite. The formation process of this microstructure could be explained by the diffusion that oversteps the solvus. The second microstructural evidence is the serrate boundary between alkali-feldspar and biotite. The projections of biotite are selectively developed next to Or lamellae of alkali-feldspar every 3-5 μm. These two microstructures would have formed as the biotite grew by consuming potash in alkali-feldspar when H2O-bearing fluid locally passed through the grain boundaries. The former microstructure was formed at 825-900 °C before lamella formation, and the latter microstructure was formed after the lamella formation. These microstructures are the indicators of fluid pathways formed under two different temperature conditions. The common coexistence of these microstructures implies that the fluid used similar pathways during the retrograde metamorphism.

  20. Alkali content of alpine ultramafic rocks

    USGS Publications Warehouse

    Hamilton, W.; Mountjoy, W.

    1965-01-01

    The lower limit of abundance of sodium and potassium in ultramafic rocks is less than the threshold amount detectable by conventional analytical methods. By a dilutionaddition modification of the flame-spectrophotometric method, sodium and potassium have been determined in 40 specimens of alpine ultramafic rocks. Samples represent six regions in the United States and one in Australia, and include dunite, peridotite, pyroxenite, and their variably serpentinized and metamorphosed derivatives. The median value found for Na2O is 0.004 per cent, and the range of Na2O is 0.001-0.19. The median value for K2O is 0.0034 per cent and the range is 0.001-0.031 per cent. Alkali concentrations are below 0.01 per cent Na2O in 28 samples and below 0.01 per cent K2O in 35. Derivation of basalt magma from upper-mantle material similar to such ultramafic rocks, as has been postulated, is precluded by the relative amounts of sodium and potassium, which are from 200 to 600 times more abundant in basalt than in the ultramafic rocks. Similar factors apply to a number of other elements. No reasonable process could produce such concentrations in, for example, tens of thousands of cubic miles of uniform tholeiitic basalt. The ultramafic rocks might have originated either as magmatic crystal precipitates or as mantle residues left after fusion and removal of basaltic magma. Injection of ultramafic rocks to exposed positions is tectonic rather than magmatic. ?? 1965.

  1. An Infrared Stimulated Luminescence (IRSL) Procedure for Estimating the Transport Rate of Potassium-Feldspar Grains in a Fluvial Setting

    NASA Astrophysics Data System (ADS)

    McGuire, C. P.; Rhodes, E. J.

    2013-12-01

    The Mojave River and Santa Clara River of Southern California were chosen as field sites to assess the feasibility of implementing infrared stimulated luminescence (IRSL) techniques to determine sediment transport rate. Feldspar sand grains in the active channel of these rivers are expected to be incompletely (partially) bleached by sunlight exposure during transport, causing the grains to have inherited charge at the time of deposition. A modification of the Post-IR IRSL procedure developed by Buylaert et al. (2009) was used for K-Feldspar grains (175-200 μm) at temperature increments of 50, 95, 140, 185, 230 °C over multiple bleach and artificial dose cycles, providing 5 signals of different sensitivity to light exposure. The measurements show an exponential decrease in equivalent dose (De) with distance down the Mojave River, with relatively less bleaching downriver for higher temperature measurements. The equivalent dose for samples at 50 °C is roughly constant along the river, at a low value of approximately 0.7 Grays. The results for higher temperature measurements suggest cyclical bleaching and burial as grains are transported downriver and higher energy (deeper) traps are gradually vacated. However, this interpretation cannot be applied to the Santa Clara River, as no simple relationship exists between the location of samples and their equivalent dose. Possible explanations for this observation include significant sediment flux from catchments with different mineralogy and recent geologic history. For the Mojave River, the relationship between De and distance downriver can be used to constrain transport rate. A bleaching experiment was designed for the Mojave River samples to assess the rate of signal loss as a function of daylight exposure time for each of the different IRSL signal components. The results for each exposure time were fit to the general order kinetics equation, a function used to fit IRSL read-out, using a non-linear regression (Levenberg

  2. Infrared Laser-Induced Breakdown Spectroscopy of Alkali Metal Halides

    NASA Astrophysics Data System (ADS)

    Brown, Ei; Hommerich, Uwe; Yang, Clayton; Trivedi, Sudhir; Samuels, Alan; Snyder, Peter

    2008-10-01

    Laser-induced breakdown spectroscopy (LIBS) is a powerful diagnostic tool for detection of trace elements by monitoring the atomic and ionic emission from laser-induced plasmas. LIBS is a relatively simple technique and has been successfully employed in applications such as environmental monitoring, materials analysis, medical diagnostics, industrial process control, and homeland security. Most LIBS applications are limited to emission features in the ultraviolet-visible-near infrared (UV-VIS-NIR) region arising from atoms and simple molecular fragments. In the present work, we report on the observation of mid- infrared emission lines from alkali metal halides due to laser-induced breakdown processes. The studied alkali metal halides included LiCl, NaCl, NaBr, KCl, KBr, KF, RbCl, and RbBr. The laser-induced plasma was produced by focusing a 16 mJ pulsed Nd:YAG laser (1064 nm) on the target. The LIBS infrared emission from alkali halides showed intense and narrow bands located in the region from 2-8 μm. The observed emission features were assigned to atomic transitions between higher-lying Rydberg states of neutral alkali atoms. More detailed results of the performed IR LIBS studies on alkali metal halides will be discussed at the conference.

  3. Multi-photon processes in alkali metal vapors

    NASA Astrophysics Data System (ADS)

    Gai, Baodong; Hu, Shu; Li, Hui; Shi, Zhe; Cai, Xianglong; Guo, Jingwei; Tan, Yannan; Liu, Wanfa; Jin, Yuqi; Sang, Fengting

    2015-02-01

    Achieving population inversion through multi-photon cascade pumping is almost always difficult, and most laser medium work under 1-photon excitation mechanism. But for alkali atoms such as cesium, relatively large absorption cross sections of several low, cascading energy levels enable them properties such as up conversion. Here we carried out research on two-photon excitation alkali fluorescence. Two photons of near infrared region are used to excite alkali atoms to n 2 D5/2, n 2 D3/2 or higher energy levels, then the blue fluorescence of (n+1) 2 P3/2,(n+1) 2 P1/2-->n 2 S1/2 are observed. Different pumping paths are tried and by the recorded spectra, transition routes of cesium are deducted and concluded. Finally the possibility of two-photon style DPALs (diode pumped alkali laser) are discussed, such alkali lasers can give output wavelengths in the shorter end of visual spectroscopy (400-460 nm) and are expected to get application in underwater communication and material laser processing.

  4. Alkali metal and rare earth element evolution of rock-forming minerals from the Gatumba area pegmatites (Rwanda): Quantitative assessment of crystal-melt fractionation in the regional zonation of pegmatite groups

    NASA Astrophysics Data System (ADS)

    Hulsbosch, Niels; Hertogen, Jan; Dewaele, Stijn; André, Luc; Muchez, Philippe

    2014-05-01

    This study presents a general model for the evaluation of Rayleigh fractional crystallisation as the principal differentiation mechanism in the formation of regionally zoned common and rare-element pegmatites. The magmatic evolution of these systems from a granitic source is reconstructed by means of alkali element and rare earth element (REE) analyses of rock-forming minerals (feldspars, micas and tourmaline), which represent a whole sequence of regional pegmatite zonation. The Gatumba pegmatite field (Rwanda, Central Africa) is chosen as case study area because of its well-developed regional zonation sequence. The pegmatites are spatially and temporally related to peraluminous G4-granites (986 ± 10 Ma). The regional zonation is developed around a G4-granite and the proximal pegmatites grade outwardly into biotite, two-mica and muscovite pegmatites. Rare-element (Nb-Ta-Sn) pegmatites occur most distal from the granite.

  5. Maternal exposure to alkali, alkali earth, transition and other metals: Concentrations and predictors of exposure.

    PubMed

    Hinwood, A L; Stasinska, A; Callan, A C; Heyworth, J; Ramalingam, M; Boyce, M; McCafferty, P; Odland, J Ø

    2015-09-01

    Most studies of metals exposure focus on the heavy metals. There are many other metals (the transition, alkali and alkaline earth metals in particular) in common use in electronics, defense industries, emitted via combustion and which are naturally present in the environment, that have received limited attention in terms of human exposure. We analysed samples of whole blood (172), urine (173) and drinking water (172) for antimony, beryllium, bismuth, cesium, gallium, rubidium, silver, strontium, thallium, thorium and vanadium using ICPMS. In general most metals concentrations were low and below the analytical limit of detection with some high concentrations observed. Few factors examined in regression models were shown to influence biological metals concentrations and explained little of the variation. Further study is required to establish the source of metals exposures at the high end of the ranges of concentrations measured and the potential for any adverse health impacts in children. PMID:25984984

  6. Maternal exposure to alkali, alkali earth, transition and other metals: Concentrations and predictors of exposure.

    PubMed

    Hinwood, A L; Stasinska, A; Callan, A C; Heyworth, J; Ramalingam, M; Boyce, M; McCafferty, P; Odland, J Ø

    2015-09-01

    Most studies of metals exposure focus on the heavy metals. There are many other metals (the transition, alkali and alkaline earth metals in particular) in common use in electronics, defense industries, emitted via combustion and which are naturally present in the environment, that have received limited attention in terms of human exposure. We analysed samples of whole blood (172), urine (173) and drinking water (172) for antimony, beryllium, bismuth, cesium, gallium, rubidium, silver, strontium, thallium, thorium and vanadium using ICPMS. In general most metals concentrations were low and below the analytical limit of detection with some high concentrations observed. Few factors examined in regression models were shown to influence biological metals concentrations and explained little of the variation. Further study is required to establish the source of metals exposures at the high end of the ranges of concentrations measured and the potential for any adverse health impacts in children.

  7. Neuropsychiatric manifestations of alkali metal deficiency and excess.

    PubMed

    Yung, C Y

    1984-01-01

    The alkali metals from the Group IA of the periodic table (lithium, sodium, potassium, rubidium, cesium and francium) are reviewed. The neuropsychiatric aspects of alkali metal deficiencies and excesses (intoxications) are described. Emphasis was placed on lithium due to its clinical uses. The signs and symptoms of these conditions are characterized by features of an organic brain syndrome with delirium and encephalopathy prevailing. There are no clinically distinctive features that could be reliably used for diagnoses. Sodium and potassium are two essential alkali metals in man. Lithium is used as therapeutic agent in bipolar affective disorders. Rubidium has been investigated for its antidepressant effect in a group of psychiatric disorders. Cesium is under laboratory investigation for its role in carcinogenesis and in depressive illness. Very little is known of francium due to its great instability for experimental study. PMID:6395136

  8. C-CAMP, A closed cycle alkali metal power system

    SciTech Connect

    Wichner, R.P.; Hoffman, H.W.

    1988-01-01

    A concept is presented for a Closed-Cycle Alkali Metal (C-CAMP) power systems which utilizes the heat of reaction of an alkali metal and halogen compound to vaporize an alkali metal turbine fluid for a Rankine cycle. Unique features of the concept are (1) direct contact (heat exchange) between the reaction products and turbine fluid, and (2) a flow-through chemical reactor/boiler. The principal feasibility issues of the concept relate to the degree of cross-mixing of product and turbine fluid streams within the reactor-boiler. If proven feasible, the concept may be adapted to a range of fuel and turbine fluids and ultimately lead to thermal efficiencies in excess of 35%.

  9. Alkali-induced enhancement of surface electronic polarizibility.

    PubMed

    Stolbov, Sergey; Rahman, Talat S

    2006-05-12

    From results of ab initio electronic structure calculations based on density functional theory for a set of prototype systems, we find alkali adsorbates to cause a dramatic enhancement of the electronic polarizability of the metal surface extending it several angstroms into the vacuum. This phenomenon is traceable to an unusual feature induced in the surface potential on alkali adsorption. The effect appears to be general, as we find it to be present on metals as varied as Pd and Cu, and helps explain the observed substantial decrease in the vibrational frequency of molecules when coadsorbed with alkalis on metal surfaces. Specifically, for two dissimilar molecules CO and O(2), we trace the softening of the frequencies of their stretching mode when coadsorbed with K on Pd(111) to the enhanced electronic polarizability.

  10. Neuropsychiatric manifestations of alkali metal deficiency and excess

    SciTech Connect

    Yung, C.Y.

    1984-01-01

    The alkali metals from the Group IA of the periodic table (lithium, sodium, potassium, rubidium, cesium and francium) are reviewed. The neuropsychiatric aspects of alkali metal deficiencies and excesses (intoxications) are described. Emphasis was placed on lithium due to its clinical uses. The signs and symptoms of these conditions are characterized by features of an organic brain syndrome with delirium and encephalopathy prevailing. There are no clinically distinctive features that could be reliably used for diagnoses. Sodium and potassium are two essential alkali metals in man. Lithium is used as therapeutic agent in bipolar affective disorders. Rubidium has been investigated for its antidepressant effect in a group of psychiatric disorders. Cesium is under laboratory investigation for its role in carcinogenesis and in depressive illness. Very little is known of francium due to its great instability for experimental study.

  11. Theoretical study of the alkali and alkaline-earth monosulfides

    NASA Technical Reports Server (NTRS)

    Partridge, Harry; Langhoff, Stephen R.; Bauschlicher, Charles W., Jr.

    1988-01-01

    Ab initio calculations have been used to obtain accurate spectroscopic constants for the X2Pi and A2Sigma(+) states of the alkali sulfides and the X1Sigma(+), a3Pi, and A1Pi states of the alkaline-earth sulfides. In contrast to the alkali oxides, the alkali sulfides are found to have X2Pi ground states, due to the larger electrostatic interaction. Dissociation energies of 3.27 eV for BeS, 2.32 eV for MgS, 3.29 eV for CaS, and 3.41 eV for SrS have been obtained for the X1Sigma(+) states of the alkaline-earth sulfides, in good agreement with experimental results. Core correlation is shown to increase the Te values for the a3Pi and A1Pi states of MgS, CaS, and SrS.

  12. 40Ar/39Ar dating of microgram feldspar grains from the paired feldspathic achondrites GRA 06128 and 06129

    NASA Astrophysics Data System (ADS)

    Lindsay, Fara N.; Herzog, Gregory F.; Park, Jisun; Delaney, Jeremy S.; Turrin, Brent D.; Swisher, Carl C.

    2014-03-01

    40Ar/39Ar ages of single feldspar grains from the paired meteorites Graves Nunatak 06128 (GRA8; 8 grains) and 06129 (GRA9; 26 grains) are presented. Plateau ages (⩾70% of the 39Ar released) ranged from 4000 to 4600 Ma with an average 1-σ uncertainty of ±90 Ma. The most precise ages obtained were 4267 ± 17 Ma for a grain from GRA8 and 4437 ± 19 Ma and 4321 ± 18 Ma for two grains from GRA9. Isotope correlation diagrams yield less precise ages ranging from 3800 to 5200 Ma with an average 1-σ uncertainty of 250 Ma; they indicate a negligible trapped component. Plateau ages, integrated total fusion ages, and isochron ages are internally concordant at the 95% confidence level. The distribution of the plateau ages for GRA9 is bimodal with peaks at 4400 and 4300 Ma. In contrast, the plateau age distribution for GRA8 peaks at about 4260 Ma with broad wings extending toward younger and older ages. To explain the distributions of grain ages we prefer a scenario that includes a major post-formation event about 4400 Ma ago and a later melt intrusion event that heated GRA8 more than some parts of GRA9.

  13. Hydrothermal chemistry, structures, and luminescence studies of alkali hafnium fluorides.

    PubMed

    Underwood, Christopher C; McMillen, Colin D; Chen, Hongyu; Anker, Jeffery N; Kolis, Joseph W

    2013-01-01

    This paper describes the hydrothermal chemistry of alkali hafnium fluorides, including the synthesis and structural characterization of five new alkali hafnium fluorides. Two ternary alkali hafnium fluorides are described: Li(2)HfF(6) in space group P31m with a = 4.9748(7) Å and c = 4.6449(9) Å and Na(5)Hf(2)F(13) in space group C2/m with a = 11.627(2) Å, b = 5.5159(11) Å, and c = 8.4317(17) Å. Three new alkali hafnium oxyfluorides are also described: two fluoroelpasolites, K(3)HfOF(5) and (NH(4))(3)HfOF(5), in space group Fm3m with a = 8.9766(10) and 9.4144(11) Å, respectively, and K(2)Hf(3)OF(12) in space group R3m with a = 7.6486(11) Å and c = 28.802(6) Å. Infrared (IR) spectra were obtained for the title solids to confirm the structure solutions. Comparison of these materials was made based on their structures and synthesis conditions. The formation of these species in hydrothermal fluids appears to be dependent upon both the concentration of the alkali fluoride mineralizer solution and the reaction temperature. Both X-ray and visible fluorescence studies were conducted on compounds synthesized in this study and showed that fluorescence was affected by a variety of factors, such as alkali metal size, the presence/absence of oxygen in the compound, and the coordination environment of Hf(4+).

  14. Spill-Resistant Alkali-Metal-Vapor Dispenser

    NASA Technical Reports Server (NTRS)

    Klipstein, William

    2005-01-01

    A spill-resistant vessel has been developed for dispensing an alkali-metal vapor. Vapors of alkali metals (most commonly, cesium or rubidium, both of which melt at temperatures slightly above room temperature) are needed for atomic frequency standards, experiments in spectroscopy, and experiments in laser cooling. Although the present spill-resistant alkali-metal dispenser was originally intended for use in the low-gravity environment of outer space, it can also be used in normal Earth gravitation: indeed, its utility as a vapor source was confirmed by use of cesium in a ground apparatus. The vessel is made of copper. It consists of an assembly of cylinders and flanges, shown in the figure. The uppermost cylinder is a fill tube. Initially, the vessel is evacuated, the alkali metal charge is distilled into the bottom of the vessel, and then the fill tube is pinched closed to form a vacuum seal. The innermost cylinder serves as the outlet for the vapor, yet prevents spilling by protruding above the surface of the alkali metal, no matter which way or how far the vessel is tilted. In the event (unlikely in normal Earth gravitation) that any drops of molten alkali metal have been shaken loose by vibration and are floating freely, a mesh cap on top of the inner cylinder prevents the drops from drifting out with the vapor. Liquid containment of the equivalent of 1.2 grams of cesium was confirmed for all orientations with rubbing alcohol in one of the prototypes later used with cesium.

  15. A comparative study of K-rich and Na/Ca-rich feldspar ice-nucleating particles in a nanoliter droplet freezing assay

    NASA Astrophysics Data System (ADS)

    Peckhaus, Andreas; Kiselev, Alexei; Hiron, Thibault; Ebert, Martin; Leisner, Thomas

    2016-09-01

    A recently designed droplet freezing assay was used to study the freezing of up to 1500 identical 0.2 nL water droplets containing suspensions of one Na/Ca-rich feldspar and three K-rich and one Na/Ca-rich feldspar particles. Three types of experiments have been conducted: cooling ramp, isothermal freezing at a constant temperature, and freeze-thaw cycles. The observed freezing behavior has been interpreted with the help of a model based on the classical nucleation theory (soccer ball model (SBM); Niedermeier et al., 2015). By applying the model to the different freezing experiments conducted with the same ice-nucleating material, the unique sets of model parameters for specific feldspar suspensions could be derived. The SBM was shown to adequately describe the observed cooling rate dependence, the ice-nucleating active sites (INAS) surface density ns(T) in a wide temperature range, and the shift of the freezing curves towards lower temperature with dilution. Moreover, the SBM was capable of reproducing the variation of INAS surface density ns(T) with concentration of ice-nucleating particles in the suspension droplets and correctly predicting the leveling-off of ns(T) at low temperature. The freeze-thaw experiments have clearly shown that the heterogeneous freezing induced even by very active ice-nucleating species still possesses a stochastic nature, with the degree of randomness increasing towards homogeneous nucleation. A population of the high-temperature INAS has been identified in one of the K-rich feldspar samples. The freezing of 0.8 wt % suspension droplets of this particular feldspar was observed already at -5 °C. These high-temperature active sites could be deactivated by treating the sample with hydrogen peroxide but survived heating up to 90 °C. Given a high mass concentration of these high-temperature active sites (2.9 × 108 g-1) and a very low value of contact angle (0.56 rad) the possibility of biological contamination of the sample was

  16. Upgrading of petroleum oil feedstocks using alkali metals and hydrocarbons

    DOEpatents

    Gordon, John Howard

    2014-09-09

    A method of upgrading an oil feedstock by removing heteroatoms and/or one or more heavy metals from the oil feedstock composition. This method reacts the oil feedstock with an alkali metal and an upgradant hydrocarbon. The alkali metal reacts with a portion of the heteroatoms and/or one or more heavy metals to form an inorganic phase separable from the organic oil feedstock material. The upgradant hydrocarbon bonds to the oil feedstock material and increases the number of carbon atoms in the product. This increase in the number of carbon atoms of the product increases the energy value of the resulting oil feedstock.

  17. Alkali Metal/Salt Thermal-Energy-Storage Systems

    NASA Technical Reports Server (NTRS)

    Phillips, Wayne W.; Stearns, John W.

    1987-01-01

    Proposed thermal-energy-storage system based on mixture of alkali metal and one of its halide salts; metal and salt form slurry of two immiscible melts. Use of slurry expected to prevent incrustations of solidified salts on heat-transfer surfaces that occur where salts alone used. Since incrustations impede heat transfer, system performance improved. In system, charging heat-exchanger surface immersed in lower liquid, rich in halide-salt, phase-charge material. Discharging heat exchanger surface immersed in upper liquid, rich in alkali metal.

  18. Metal induced gap states at alkali halide/metal interface

    NASA Astrophysics Data System (ADS)

    Kiguchi, Manabu; Yoshikawa, Genki; Ikeda, Susumu; Saiki, Koichiro

    2004-10-01

    The electronic state of a KCl/Cu(0 0 1) interface was investigated using the Cl K-edge near-edge X-ray absorption fine structure (NEXAFS). A pre-peak observed on the bulk edge onset of thin KCl films has a similar feature to the peak at a LiCl/Cu(0 0 1) interface, which originates from the metal induced gap state (MIGS). The present result indicates that the MIGS is formed universally at alkali halide/metal interfaces. The decay length of MIGS to an insulator differs from each other, mainly due to the difference in the band gap energy of alkali halide.

  19. Feasibility of supersonic diode pumped alkali lasers: Model calculations

    SciTech Connect

    Barmashenko, B. D.; Rosenwaks, S.

    2013-04-08

    The feasibility of supersonic operation of diode pumped alkali lasers (DPALs) is studied for Cs and K atoms applying model calculations, based on a semi-analytical model previously used for studying static and subsonic flow DPALs. The operation of supersonic lasers is compared with that measured and modeled in subsonic lasers. The maximum power of supersonic Cs and K lasers is found to be higher than that of subsonic lasers with the same resonator and alkali density at the laser inlet by 25% and 70%, respectively. These results indicate that for scaling-up the power of DPALs, supersonic expansion should be considered.

  20. Interfacial tension in immiscible mixtures of alkali halides.

    PubMed

    Lockett, Vera; Rukavishnikova, Irina V; Stepanov, Victor P; Tkachev, Nikolai K

    2010-02-01

    The interfacial tension of the liquid-phase interface in seven immiscible reciprocal ternary mixtures of lithium fluoride with the following alkali halides: CsCl, KBr, RbBr, CsBr, KI, RbI, and CsI was measured using the cylinder weighing method over a wide temperature range. It was shown that for all mixtures the interfacial tension gradually decreases with growing temperature. The interfacial tension of the reciprocal ternary mixtures at a given temperature increases both with the alkali cation radius (K(+) < Rb(+) < Cs(+)) and with the radius of the halogen anion (Cl(-) < Br(-) < I(-)). PMID:20094678

  1. Ternary alkali-metal and transition metal or metalloid acetylides as alkali-metal intercalation electrodes for batteries

    SciTech Connect

    Nemeth, Karoly; Srajer, George; Harkay, Katherine C; Terdik, Joseph Z

    2015-02-10

    Novel intercalation electrode materials including ternary acetylides of chemical formula: A.sub.nMC.sub.2 where A is alkali or alkaline-earth element; M is transition metal or metalloid element; C.sub.2 is reference to the acetylide ion; n is an integer that is 0, 1, 2, 3 or 4 when A is alkali element and 0, 1, or 2 when A is alkaline-earth element. The alkali elements are Lithium (Li), Sodium (Na), Potassium (K), Rubidium (Rb), Cesium (Cs) and Francium (Fr). The alkaline-earth elements are Berilium (Be), Magnesium (Mg), Calcium (Ca), Strontium (Sr), Barium (Ba), and Radium (Ra). M is a transition metal that is any element in groups 3 through 12 inclusive on the Periodic Table of Elements (elements 21 (Sc) to element 30 (Zn)). In another exemplary embodiment, M is a metalloid element.

  2. 238U-230Th-226Ra disequilibria in dacite and plagioclase from the 2004-2005 eruption of Mount St. Helens: Chapter 36 in A volcano rekindled: the renewed eruption of Mount St. Helens, 2004-2006

    USGS Publications Warehouse

    Cooper, Kari M.; Donnelly, Carrie T.; Sherrod, David R.; Scott, William E.; Stauffer, Peter H.

    2008-01-01

    230Th)/(232Th) measured for the 1980s reference suite. However, (230Th)/(232Th) for plagioclase separates for dome samples erupted during October and November 2004 are significantly different from corresponding whole-rock values, which suggests that a large fraction (>30 percent) of crystals in each sample are foreign to the host liquid. Furthermore, plagioclase in the two 2004 samples have U-series characteristics distinct from each other and from plagioclase in dacite erupted in 1982, indicating that (1) the current eruption must include a component of crystals (and potentially associated magma) that were not sampled by the 1980-86 eruption, and (2) dacite magmas erupted only a month apart in 2004 contain different populations of crystals, indicating that this foreign component is highly heterogeneous within the 2004-5 magma reservoir.

  3. K-feldspar-muscovite-andalusite-quartz-brine phase equilibria: An experimental study at 25 to 60 MPa and 400 to 550 C

    SciTech Connect

    Frank, M.R.; Candela, P.A.; Piccoli, P.M.

    1998-12-01

    Felsic magmas may evolve one or more water or chlorine-rich fluid phases which can transport heat and solutes into associated hydrothermal systems and can contribute to alteration and ore deposition. To understand the role of a high-salinity aqueous phase in the magmatic hydrothermal environment, the composition of a subcritical, vapor-undersaturated high-salinity liquid phase (brine) in equilibrium with K-feldspar-muscovite-quartz and muscovite-andalusite-quartz was determined for pressures and temperatures ranging from 25 MPa and 400 C to 60 MPa and 550 C, with total Cl (NaCl + KCl + HCl) concentrations ranging from 3.42 to 8.56 (moles of solute/kg solution). Comparison of results with previous studies conducted at higher pressures and lower-salinity aqueous phases show that the mineral stability fields in the K-feldspar-muscovite-andalusite-quartz system shift to lower KCl/KCl values with increasing salinity and decreasing pressure.

  4. 40 CFR 721.5985 - Fatty alkyl phosphate, alkali metal salt (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Fatty alkyl phosphate, alkali metal... Specific Chemical Substances § 721.5985 Fatty alkyl phosphate, alkali metal salt (generic). (a) Chemical... as a fatty alkyl phosphate, alkali metal salt (PMN P-99-0385) is subject to reporting under...

  5. 40 CFR 721.5985 - Fatty alkyl phosphate, alkali metal salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Fatty alkyl phosphate, alkali metal... Specific Chemical Substances § 721.5985 Fatty alkyl phosphate, alkali metal salt (generic). (a) Chemical... as a fatty alkyl phosphate, alkali metal salt (PMN P-99-0385) is subject to reporting under...

  6. 40 CFR 721.5985 - Fatty alkyl phosphate, alkali metal salt (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Fatty alkyl phosphate, alkali metal... Specific Chemical Substances § 721.5985 Fatty alkyl phosphate, alkali metal salt (generic). (a) Chemical... as a fatty alkyl phosphate, alkali metal salt (PMN P-99-0385) is subject to reporting under...

  7. 40 CFR 721.5985 - Fatty alkyl phosphate, alkali metal salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Fatty alkyl phosphate, alkali metal... Specific Chemical Substances § 721.5985 Fatty alkyl phosphate, alkali metal salt (generic). (a) Chemical... as a fatty alkyl phosphate, alkali metal salt (PMN P-99-0385) is subject to reporting under...

  8. 40 CFR 721.5985 - Fatty alkyl phosphate, alkali metal salt (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Fatty alkyl phosphate, alkali metal... Specific Chemical Substances § 721.5985 Fatty alkyl phosphate, alkali metal salt (generic). (a) Chemical... as a fatty alkyl phosphate, alkali metal salt (PMN P-99-0385) is subject to reporting under...

  9. 40 CFR 721.5452 - Alkali metal salt of halogenated organoborate (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Alkali metal salt of halogenated... Specific Chemical Substances § 721.5452 Alkali metal salt of halogenated organoborate (generic). (a... generically as alkali metal salt of halogenated organoborate (PMN P-00-0638) is subject to reporting...

  10. 40 CFR 721.5452 - Alkali metal salt of halogenated organoborate (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkali metal salt of halogenated... Specific Chemical Substances § 721.5452 Alkali metal salt of halogenated organoborate (generic). (a... generically as alkali metal salt of halogenated organoborate (PMN P-00-0638) is subject to reporting...

  11. 40 CFR 721.5452 - Alkali metal salt of halogenated organoborate (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alkali metal salt of halogenated... Specific Chemical Substances § 721.5452 Alkali metal salt of halogenated organoborate (generic). (a... generically as alkali metal salt of halogenated organoborate (PMN P-00-0638) is subject to reporting...

  12. 40 CFR 721.5452 - Alkali metal salt of halogenated organoborate (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Alkali metal salt of halogenated... Specific Chemical Substances § 721.5452 Alkali metal salt of halogenated organoborate (generic). (a... generically as alkali metal salt of halogenated organoborate (PMN P-00-0638) is subject to reporting...

  13. 40 CFR 721.5452 - Alkali metal salt of halogenated organoborate (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alkali metal salt of halogenated... Specific Chemical Substances § 721.5452 Alkali metal salt of halogenated organoborate (generic). (a... generically as alkali metal salt of halogenated organoborate (PMN P-00-0638) is subject to reporting...

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

    NASA Technical Reports Server (NTRS)

    Santosh, M.; Drury, S. A.; Iyer, S. S.

    1988-01-01

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

  15. Assesment of Alkali Resistance of Basalt Used as Concrete Aggregates

    NASA Astrophysics Data System (ADS)

    al-Swaidani, Aref M.; Baddoura, Mohammad K.; Aliyan, Samira D.; Choeb, Walid

    2015-11-01

    The objective of this paper is to report a part of an ongoing research on the influence of using crushed basalt as aggregates on one of durability-related properties of concrete (i.e. alkali-silica reaction which is the most common form of Alkali-Aggregate Reaction). Alkali resistance has been assessed through several methods specified in the American Standards. Results of petrographic examination, chemical test (ASTM C289) and accelerated mortar bar test (ASTM C1260) have particularly been reported. In addition, the weight change and compressive strength of 28 days cured concrete containing basaltic aggregates were also reported after 90 days of exposure to 10% NaOH solution. Dolomite aggregate were used in the latter test for comparison. The experimental results revealed that basaltic rocks quarried from As-Swaida'a region were suitable for production of aggregates for concrete. According to the test results, the studied basalt aggregates can be classified as innocuous with regard to alkali-silica reaction. Further, the 10% sodium hydroxide attack did not affect the compressive strength of concrete.

  16. Chlor-Alkali Industry: A Laboratory Scale Approach

    ERIC Educational Resources Information Center

    Sanchez-Sanchez, C. M.; Exposito, E.; Frias-Ferrer, A.; Gonzalez-Garaia, J.; Monthiel, V.; Aldaz, A.

    2004-01-01

    A laboratory experiment for students in the last year of degree program in chemical engineering, chemistry, or industrial chemistry is presented. It models the chlor-alkali process, one of the most important industrial applications of electrochemical technology and the second largest industrial consumer of electricity after aluminium industry.

  17. Influence of temperature on alkali stress adaptation in Listeria monocytogenes

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Listeria monocytogenes cells may induce alkali stress adaptation when exposed to sublethal concentrations of alkaline cleaners and sanitizers that may be frequently used in the food processing environment. In the present study, the effect of temperature on the induction and the stability of such alk...

  18. 40 CFR 721.8900 - Substituted halogenated pyridinol, alkali salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.8900 Substituted halogenated pyridinol, alkali salt. (a) Chemical substances and significant new uses subject to reporting. (1) The chemical substances identified...

  19. Stabilized Alkali-Metal Ultraviolet-Band-Pass Filters

    NASA Technical Reports Server (NTRS)

    Mardesich, Nick; Fraschetti, George A.; Mccann, Timothy; Mayall, Sherwood D.; Dunn, Donald E.; Trauger, John T.

    1995-01-01

    Layers of bismuth 5 to 10 angstrom thick incorporated into alkali-metal ultraviolet-band-pass optical filters by use of advanced fabrication techniques. In new filters layer of bismuth helps to reduce surface migration of sodium. Sodium layer made more stable and decreased tendency to form pinholes by migration.

  20. Factors associated with alkali production from arginine in dental biofilms.

    PubMed

    Huang, X; Exterkate, R A M; ten Cate, J M

    2012-12-01

    Alkali production by oral bacteria in the oral cavity has been linked to protection against dental caries. The current study assessed various parameters associated with ammonium produced during arginine catabolism in dental biofilms. Polymicrobial biofilms were formed with saliva as the inoculum. The NH(3) level and the pH of the spent medium were used to monitor and quantitate the bacterial reactions. The presence of sucrose, a low buffer capacity, and a low pH (≤ pH 4.5) were found to hamper alkali production from arginine. The rate of alkali production exhibited an optimum around pH 5.5. Biofilms were found to produce NH(3) also from polypeptides and proteins in the medium. The biofilm age affected these processes. The experimental model proved valuable for the assessment of the collective bacterial reactions determining the overall pH outcome. This experimental approach could bridge the gap in our knowledge between pH-rise phenomena and caries susceptibility from clinical observations and studies performed on alkali-producing bacteria in well- controlled, though simplified, in vitro models. Analysis of our data supports the hypothesis that the initiation and progression of dental caries may be influenced by the relative rates of acid and base formation, which critically depend on the aforementioned parameters. PMID:23010718