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1.
Solubility of Anhydrite, CaSO4, in NaCl-H2O Solutions at High Pressures and Temperatures: Applications to Fluid-Rock Interaction 总被引：1，自引：0，他引：1
Anhydrite solubility in H2O–NaCl solutions was measuredat 6–14 kbar, 600–800°C and NaCl mole fractions(XNaCl) of 0–0·3 in piston–cylinder apparatus.Solubilities were determined by weight changes of natural anhydritein perforated Pt envelopes confined with fluid in larger Ptcapsules. In initially pure H2O at 10 kbar and 800°C, CaSO4concentration is low (0·03 molal), though much largerthan at the same temperature and 1 kbar. Hematite-buffered experimentsshowed slightly lower solubilities than unbuffered runs. CaSO4solubility increases enormously with NaCl activity: at 800°Cand 10 kbar and XNaCl of 0·3, CaSO4 molality is 200 timeshigher than with pure H2O. Whereas CaSO4 solubility in pureH2O decreases with rising T at low T and P, the high-P resultsshow that anhydrite solubility increases with T at constantP at all XNaCl investigated. The effects of salinity and temperatureare so great at 10 kbar that critical mixing between sulfate-richhydrosaline melts and aqueous salt solutions is probable at900°C at XNaCl 0·3. Recent experimental evidencethat volatile-laden magmas crystallizing in the deep crust mayevolve concentrated salt solutions could, in light of the presentwork, have important implications regarding such diverse processesas Mount Pinatubo-type S-rich volcanism, high-f O2 regionalmetamorphism, and emplacement of porphyry Cu–Mo ore bodies,where anhydrite–hematite alteration and fluid inclusionsreveal the action of very oxidized saline solutions rich insulfur. KEY WORDS: anhydrite; sulfur; solubility; metamorphic brines; granulites 相似文献
2.
Properly designed precast concrete cladding could potentially provide lateral stiffness, ductility, and energy dissipation for an overall building structure, especially during earthquakes. This paper describes a set of advanced connections that take advantage of the interaction between facade panels and structure (mainly due to horizontal interstorey drift) to dissipate energy, thereby reducing the response of the main structure. The results of an experimental program to characterize the hysteretic behaviour of advanced connections are presented. Design equations for the advanced connections are then calibrated against the test results, and the corresponding design charts are presented. It is anticipated that this research will lead to innovative ways of viewing the entire cladding system of a building. 相似文献
3.
Late Cretaceous epicontinental phosphorites, porcelanites/cherts, dark-coloured shales, glauconitic sandstones and bioclastic and fine-grained carbonate rocks in Egypt are examined in terms of their overall depositional and diagenetic framework and stable isotopic and organic geochemical characteristics. Two main depositional realms are interpreted and correlated through sequence stratigraphic analysis: (1) a shallow hemipelagic environment accompanying initial stages of marine transgression and conducive to the formation of organic carbon-rich shales, biosiliceous sediments and thick phosphorites, and (2) a relatively high energy depositional regime accompanying sea-level fall during which deltas advanced, glauconites were reworked seaward and prograding oyster banks became periodically exposed to episodes of fresh water diagenesis, thereby promoting solution-collapse phenomena in associated cherts. Lenticular to massive phosphorites are viewed as the result of current winnowing and concentration of authigenic grains initially precipitated in associated reducing shales and biosiliceous sediments. In eastern Egypt the phosphorites form winnowed lag layers, some of which may have been redeposited down slope in structural lows. In the west, these sands were concentrated into giant phosphorite sand waves built by reworking of penecontemporaneously deposited phosphatic muds during marine transgression. Carbon isotopic results substantiate interpretations from modern deposits for limitation of phosphate mineral precipitation with depth in sediments as a result of lattice poisoning. However, direct desorption of phosphorus to pore waters from detrital iron-oxyhydroxide phases also may have been important in the Cretaceous setting, the iron reduced in this process being available for incorporation in glauconites. The main locus for authigenic glauconite precipitation appears to be where iron fluxes from regions of lateritic weathering were highest and near the boundary between oxygenated and reduced waters. This study suggests a model for the common coexistence of glauconites and phosphorites in the geological record. Although upwelling is often advocated as the origin of nearly all giant phosphorite deposits, we suggest that some of these may have been strongly influenced by fluvially derived phosphorus borne on particulates and desorbed from these compounds upon flocculation and/or reduction in bottom waters or pore waters. 相似文献
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BRIAR CRAIG 《Geographical review》2013,103(2):210-218
5.
Abstract— To investigate the nature, origin, and history of the fine‐grained matrix in Semarkona and develop techniques suitable for small samples, we have measured the induced thermoluminescence properties of six matrix samples 10 μm to 400 μm in size. The samples had TL sensitivities comparable with 4 mg of bulk samples of type 3.2–3.4 ordinary chondrites, which is very high relative to bulk Semarkona. The other induced TL properties of these samples, TL peak temperatures, and TL peak widths distinguish them from other ordinary chondrite samples where the TL is caused by feldspar. Cathodoluminescence images and other data suggest that the cause of the luminescence in the Semarkona fine‐grained matrix is forsterite. In some respects the matrix TL data resemble that of Semarkona chondrules, in which the phosphor is forsterite and terrestrial forsterites from a variety of igneous and metamorphic environments. However, differences in the TL peak temperature versus TL peak width relationship between the matrix samples and the other forsterites suggest a fundamentally different formation mechanism. We also note that forsterite appears to be a major component in many primitive materials, such as nebulae, cometary dust, and Stardust particles. 相似文献
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Evolving factor analysis is used to estimate the concentration profiles and spectra of Bi~(3 )and the bismuthchloride complexes BiCl~(2 )through BiCl_6~(3-)formed by injection of bismuth percblorate into a flowingstream of 1.0 mol l~(-1) HCl.The estimated spectra compare favorably with previously published spectraof the complexes. 相似文献
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The South Auckland Volcanic Field is a Pleistocene (1·59–0·51Ma) basaltic intraplate, monogenetic field situated south ofAuckland City, North Island, New Zealand. Two groups of basaltsare distinguished based on mineralogy and geochemical compositions,but no temporal or spatial patterns exist in the distributionof various lava types forming each group within the field: GroupA basalts are silica-undersaturated transitional to quartz-tholeiiticbasalts with relatively low total alkalis (3·0–4·6wt %), Nb (7–29 ppm), and (La/Yb)N (3·4–7·6);Group B basalts are strongly silica-undersaturated basanitesto nepheline-hawaiites with high total alkalis (3·3–7·9wt %), Nb (32–102 ppm), and (La/Yb)N (12–47). GroupA has slightly higher 87Sr/86Sr, similar Nd, and lower 206Pb/204Pbvalues compared with Group B. Contrasting geochemical trendsand incompatible element ratios (e.g. K/Nb, Zr/Nb, Ce/Pb) areconsistent with separate evolution of Groups A and B from dissimilarparental magmas derived from distinct sub-continental lithosphericmantle sources. Differentiation within each group was controlledby olivine and clinopyroxene fractionation. Group B magmas weregenerated by <8% melting of an ocean island basalt (OIB)-likegarnet peridotite source with high 238U/204Pb mantle (HIMU)and enriched mantle (EMII) characteristics possibly inheritedfrom recycled oceanic crust. Group A magmas were generated by<12% melting of a spinel peridotite source also with HIMUand EMII signatures. This source type may have resulted fromsubduction-related metasomatism of the sub-continental lithospheremodified by a HIMU plume. These events were associated withMesozoic or earlier subduction- and plume-related magmatismwhen New Zealand was at the eastern margin of the Gondwana supercontinent. KEY WORDS: continental intraplate basalts; geochemistry; HIMU, EMII; Sr, Nd, and Pb isotopes; South Auckland; sub-continental lithospheric sources 相似文献
8.
J.CRAIG HAMILTON Shared Research Resource Laboratories School of Medicine East Carolina University Greenville NC U.S.A.PAUL J.GEMPERLINE Department of Chemistry East Carolina University Greenville NC U.S.A. 《地理学报(英文版)》1990,(1)
One of the major applications of factor analysis in the chemical literature,self-modeling curve resolution(SMCR),is covered in this review,including a historical account of the inethods derived from Lawtonand Sylvestre's original method.Papers treating the theory or applications of SMCR are included.Qualitative and quantitative applications are described where appropriate. 相似文献
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Abstract Standard petrographic, microthermometric and Raman spectroscopic analyses of fluid inclusions from the metamorphosed massive sulphide deposits at Ducktown, Tennessee, indicate that fluids with a wide range of compositions in the C–O–H–N–S–salt system were involved in the syn- to post-metamorphic history of these deposits. Primary fluid inclusions from peak metamorphic clinopyroxene contain low-salinity, H2O–CH4 fluids and calcite, quartz and pyrrhotite daughter crystals. Many of these inclusions exhibit morphologies resembling those produced in laboratory experiments in which confining pressures significantly exceed the internal pressures of the inclusions. Secondary inclusions in metamorphic quartz from veins, pods, and host matrix record a complex uplift history involving a variety of fluids in the C–O–H–N–salt system. Early fluids were generated by local devolatilization reactions while later fluids were derived externally. Isochores calculated for secondary inclusions in addition to the chronology of trapping and morphological features of primary and secondary fluid inclusions suggest an uplift path which was concave toward the temperature axis over the P–T range 6–3 kbar and 550–225° C. Immiscible H2O–CH4–N2–NaCl fluids were trapped under lithostatic to hydrostatic pressure conditions at 3–0.5 kbar and 215 ± 20° C. Entrapment occurred during Alleghanian thrusting, and the fluids may have been derived by tectonically driven expulsion of pore fluids and thermal maturation of organic material in lower-plate sedimentary rocks which are thought to underlie the deposits. Episodic fracturing and concomitant pressure decreases in upper-plate rocks, which host the ore bodies, would have allowed these fluids to move upward and become immiscible. Post-Alleghanian uplift appears to have been temperature-convex. Uplift rates of 0.10–0.05 mm year?1 from middle Ordovician to middle Silurian – late Devonian, and 0.07–0.12 mm year?1 from middle Silurian – late Devonian to late Permian are suggested by our uplift path and available geochronological data. 相似文献
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