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1.
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2.
Transient growth of an isolated bubble in muddy, fine-grained sediments   总被引：2，自引：0，他引：2  
Methane bubbles in fine-grained sediments have been shown to grow initially by elastic expansion and fracture. A previous growth model assumed quasi-steady state diffusion in which the methane porewater concentration quickly adjusted to changes in bubble geometry [Gardiner B. S, Boudreau B. P and Johnson B. D. (2003a) Growth of disk-shaped bubbles in sediments. Geochim. Cosmochim. Acta, 67 (8), 1485-1494]. Here, we present a finite-element model that solves the transient form of the reaction-diffusion equation, and the coupled linear elastic fracture mechanics (LEFM). In so doing we also employ a new theory for the post-fracture bubble sizes, based upon the full principles of LEFM.Our findings indicate that the quasi-steady state assumption is flawed due to violation of conservation of mass during fracture events. When the new model is applied to sediment conditions found at Cape Lookout Bight, NC, USA, it is found that bubbles grow somewhat faster than previously thought. A reference bubble of 0.5 cm3 will form in about 6 days, 2.5 days quicker than the old model predicted. Moreover, typical bubbles of 0.04 cm3 for this site can grow in as little as a day and a half. We examined the sensitively of the finite-element model to the various parameters in order to gain an understanding of how bubbles may behave under different sediment conditions. The influence of tides on bubble growth, through the process of rectified diffusion, was also examined and it was found that this had little influence upon growth.  相似文献   

3.
爆炸式喷发过程中,火山碎屑物气孔记录了挥发分出溶、膨胀和合并等信息,其大小、形态、数量密度、空间分布等局域特征是推断火山喷发动力条件的重要参考。文章基于天池火山三期喷发(50 000年前大喷发的黄色浮岩、千年大喷发的灰白色浮岩和1668年八卦庙期喷发的黑色浮岩)野外地质工作,以非线性火山喷发动力学为指导,开展了火山通道内气泡生长的流体动力学研究,揭示出岩浆流体黏性力和界面张力的共同作用对于岩浆减压和气泡生长过程的约束。在浮岩气孔结构的定量化分析基础上,进一步研究了天池火山三期喷发的浮岩气孔参数,通过气泡生长流体动力学方程得到了千年大喷发灰白色浮岩毛细管数Ca值为253, 明显高于50 000年前大喷发黄色浮岩(Ca值为94)和八卦庙期喷发黑色浮岩(Ca值为111),表明了千年大喷发曾发生过明显的成分变化,推测可能与幔源基性岩浆注入有关;而50 000年前大喷发黄色浮岩气孔不规则形态参数(1-Ω)值为0.098,大于后两期喷发(分别为0.052和0.064),可能意味着天池火山系统动力学平衡的弛豫周期变小或浮岩气泡生长受动力学、流变学改造过程减弱,这可为进一步研究天池火山活动规律提供参考。三期浮岩毛细管数Ca量级为102,气孔不规则形态参数(1-Ω)量级为10-1,从动力学上首次证实了天池火山属于普林尼型或超普林尼型喷发。  相似文献   

4.
Conventional and non-conventional flotation for mineral processing and for water (and wastewaters) treatment and reuse (or recycling) is rapidly broadening their applications in the mining field. Conventional flotation assisted with microbubbles (30–100 μm) finds application in the recovery of fine mineral particles (< 13 μm) and flotation with these fine bubbles is being used as a solid/liquid separation to remove pollutants. The injection of small bubbles to conventional coarse bubbles flotation cells usually leads to general improvements of the separation parameters, especially for the ultrafines (< 5 μm) ore particles. Results obtained are believed to occur by enhancing the capture of particles by bubbles, one of the main drawbacks in fine ore flotation. It is believed that by decreasing the bubble size distribution (through the injection of small bubbles), increases the bubble surface flux and the fines capture. DAF or dissolved air flotation with microbubbles, treating water, wastewater and domestic sewage is known for a number of years and is now gradually entering in the mining environmental area. This technology offers, in most cases, advantages over settling, filtration, precipitation, or adsorption onto natural and synthetic adsorbents. The targets are the removal of oils (emulsified or not), ions (heavy metals and anions) and the reuse or recirculation of the process waters. Advantages include better treated water quality, rapid start up, high rate operation, and a thicker sludge. New applications are found in the mining vehicles washing water treatment and reuse, AMD (acid mining drainage) neutralization and high rate solids/water separation by flotation with microbubbles. This work reviews some recent applications of the use of microbubbles to assist the recovery of very small mineral particles and for the removal of pollutants from mining wastewaters. Emphasis is given to the design features of innovative devices showing the potential of conventional and unconventional DAF flotation.  相似文献   

5.
Bubble growth experiments were performed in a piston-cylinder by hydrating albite melt with ∼11 wt.% H2O at 550 MPa followed by rapid decompression at 1 MPa s−1 to pressures of 450 or 400 MPa. At these conditions the melt was supersaturated with ∼0.5 or ∼1.5 wt.% H2O, respectively, which caused rapid exsolution and bubble growth. Results at 1200 °C demonstrate that portions of the initial cumulative bubble-area distributions may be characterized by a power law with an exponent near 1, but they rapidly evolve to exponential distributions and approach a unimodal distribution after 32 h of growth. This evolution occurs by the growth of larger bubbles at the expense of smaller ones. The growth rate of the average bubble radius in these experiments is described by a power law whose exponent is 0.35, close to the theoretical exponent of 1/3 for phase growth in which coalescence is dominated by Ostwald ripening of the bubbles. Over the range of pressures and water contents investigated at 1200 °C, the bubble-size distributions and growth rate are not significantly affected by changes in the amount of exsolved water or by splitting the decompression path into two steps. Similar decompression experiments at 800 °C are dominated by smaller bubbles than in the 1200 °C experiments and also demonstrate exponential cumulative size distributions, but consistently contain a small fraction of larger bubbles. The growth rate of these bubble radii cannot be fit with a power law, but a logarithmic dependence of the bubble radii on time is possible, suggesting a difference in the growth mechanisms at low and high temperatures. This difference is attributed to the orders of magnitude changes in melt viscosity and water diffusion in the melt as the temperature varies from 800 to 1200 °C. At 1200 °C the transport properties of albite melt resemble those of natural basaltic melts whereas at 800 °C the properties are similar to those of andesitic to dacitic melts. The decompression rate used in this study exceeds natural rates by one to two orders of magnitude. Thus, these results indicate that natural mafic-to-intermediate magmas supersaturated with only a small excess of water should easily nucleate bubbles during ascent and that bubble growth in mafic magmas will proceed much more rapidly than in andesitic to dacitic magmas. Intermediate composition magmas also may be capable of forming bimodal bubble-size distributions even in the case when only one nucleation event occurred. The rapid evolution of the bubble-size distribution from a power law to an exponential may be useful in constraining the time duration between bubble nucleation and the quenching of natural samples.  相似文献   

6.
Transport of trace metals by natural organic matter (NOM) is potentially an important vector for trace metal incorporation in secondary cave precipitates [speleothems], yet little is known about the size distribution, speciation and metal binding properties of NOM in cave dripwaters. A hyperalkaline cave environment (ca. pH 11) was selected to provide information on colloid-metal interactions in cave waters, and to address the lack of high-pH data in natural systems in general. Colloidal (1 nm-1 μm) NOM in hyperalkaline cave dripwater from Poole’s Cavern, UK, was characterised by flow field-flow fractionation (FlFFF) coupled to UV and fluorescence detectors and transmission electron microscopy (TEM) coupled to X-ray energy-dispersive spectroscopy (X-EDS); trace-metal lability was examined by diffusive gradients in thin films (DGT). Colloidal aggregates and small particulates (>1 μm) imaged by TEM were morphologically heterogeneous with qualitative elemental compositions (X-EDS spectra; n = 41) consistent with NOM aggregates containing aluminosilicates, and iron and titanium oxides. Globular organic colloids, with diameters between ca. 1 and 10 nm were the most numerous colloidal class and exhibited high UV-absorbance (254 nm) and fluorescence intensity (320:400 nm excitation: emission) in optical regions characteristic of humic-like compounds. Metal binding with humic substances was modelled using the WHAM 6.1 (model VI) and visual MINTEQ 3.0 (NICA-Donnan) speciation codes. At pH 11, both models predicted dominant humic binding of Cu (ca. 100%) and minimal binding of Ni and Co (ca. <1-7%). A DGT depletion experiment (7 days duration) with the hyperalkaline dripwater showed that the available proportion of each metal was much lower than its total concentration. Metal availability for DGT in the initial stages (24 h) was consistent with weaker binding of alkaline earth metals by humic substances (Ba > Sr > V > Cu > Ni > Co), compared to the transition metals. Integrated over the entire experiment, the DGT-available proportion of transition metals (Ni > Cu & V >> Co) differed greatly from the expected hierarchy from WHAM and MINTEQ, indicating unusually strong complexation of Co. Total metal concentrations of Cu, Ni, and Co in raw and filtered PE1 dripwater samples (n = 53) were well correlated (Cu vs. Ni, R2 = 0.8; Cu vs. Co, R2 = 0.5) and were strongly reduced (> ca. 50%) by filtration at ca. 100 and 1 nm, indicating a common colloidal association. Our results demonstrate that soil-derived colloids reach speleothems, despite transport through a karst zone with potential for adsorption, and that NOM is a dominant complexant of trace metals in high pH speleothem-forming groundwaters.  相似文献   

7.
Bubble-induced porewater mixing: A 3-D model for deep porewater irrigation   总被引：1，自引：0，他引：1  
Porewater data from vent sites of the northeastern shelf off Sakhalin Island, Sea of Okhotsk, exhibit bottom-water concentrations down to a sediment depth of up to 300 cm. Below this depth, solute concentrations rapidly change due to methanogenesis and anaerobic methane oxidation (AMO). The profile shapes suggest an irrigation-like process that mixes on a meter scale. At these sites active gas emanation into the overlying water column and near-surface gas hydrates are commonly observed. We propose that methane gas bubbles rise through the soft surface sediments and cause mixing of the porewater.Mathematically, the bubble-induced irrigation can be described by eddy diffusion enhancing the diffusive transport of solutes by several orders of magnitude. A 3-D numerical transport-reaction model was developed to investigate the parameters defining the mixing process, such as bubble rise velocity, tube size, tube distribution in the sediment, and ebullition frequency.Model consistency with the field data requires eddy diffusivities ?1 × 105 cm2/a, tube densities of >4 tubes/m2 (equivalent to a tube spacing of <40 cm), active gas seepage for more than a few weeks or months, and moderate to low diagenetic reaction rates of solutes. The corresponding methane gas fluxes that are predicted from the results of the model realizations range from 1 × 103-5 × 105 L/(m2 a). Due to bubble mixing, solute fluxes in these sediments are increased by a factor of 3 and the maximum AMO rate by a factor of 7.  相似文献   

8.
The comparative behaviour of Ni, Cu and Zn in the system “mine tailings–ground water–plants” has been investigated at the Ni–Cu mine site operated by INCO Ltd. Thompson Operations, Thompson, Manitoba. Oxidation of sulphide minerals causes the release of metals from exposed tailings containing Ni ∼2000 ppm, Cu ∼150 ppm and Zn ∼100 ppm to the ground water, which contains 350 mg/L Ni, 0.007 mg/L Cu, and 1.6 mg/L Zn. The metal concentration in the ground water is affected by the relative proportions of sulfide minerals, the rate of oxidation of sulphide minerals (Ni-bearing pyrrhotite > sphalerite > chalcopyrite), and the affinity of the metals for secondary Fe-phases (Ni > Zn > Cu).  相似文献   

9.
Bubble size distributions and flotation rates were determined as a function of air flow rate and frother concentration using a specially designed batch flotation cell. This cell permitted the unambiguous determination of the flotation rate from the slurry to the froth.Flotation rate constants were determined for different size classes of silica and galena. The flotation rate constants increased to a maximum and then decreased as air flow rate was increased. This maximum was predicted by a model which considered the effect of bubble size on both the total bubble surface area and the bubble-particle collision efficiency. This work shows that collision efficiency effects, shown to exist in single-bubble/single-particle systems, are also present in flotation systems where many bubbles and particles interact.A second model for hindered flotation is proposed which assumes that the particle-capturing bubble surface differs from the particle-retaining surface. This model predicts a sharp transition from hindered to free flotation. Experimental results are presented which agree well with those derived from the model.  相似文献   

10.
Studies have shown that using organic coated bubbles (“oily” bubbles) could increase bitumen recovery rate in flotation. One way to coat bubbles is that used in the air-assisted solvent extraction process where solvent foam is formed and injected through a capillary to release solvent coated bubbles in a controlled manner into the aqueous system. To investigate adapting this approach, the foaming properties of some organics (Hexane, Heptane, Hexadecane, Petroleum Ether, Toluene, Benzene and Kerosene and their binary mixtures) of potential interest in oily bubble bitumen flotation were investigated. Silicone oil was found to be a good foaming agent in some cases. Bubble stability and film thickness experiments were carried out to help select candidate organics. Surface tension and dynamic viscosity measurements were conducted to examine the mechanism of foaming. Attachment studies showed that droplets of the selected organics readily attached to a bitumen surface compared to air bubbles. From a combination of criteria, 25:75 Hexadecane/Heptane appears to be a promising candidate.  相似文献   

11.
Little is known about the presence, distribution and size of bubbles in rhyolitic magmas prior to eruption. Using X-ray tomography to study pumice from early-erupted Bishop rhyolite, we discovered a large vesicle with abundant magnetite crystals attached to its walls. Attachment of magnetite crystals to bubble walls under pre-eruptive conditions can explain the cluster of magnetite crystals as a result of bubbles rising and collecting magnetite crystals. Alternatively, bubbles may have nucleated on magnetite crystals and then coalesced to form one large bubble with multiple magnetite crystals attached to it. We argue that the clusters of magnetite crystals could not have formed during or after eruptive decompression, and conclude that this vesicle corresponds to a bubble present prior to eruptive decompression. The inferred presence of pre-eruptive bubbles in the Bishop magma confirms the interpretation that the magma was volatile-saturated prior to eruption. The pre-eruptive size of this bubble is estimated based on three independent approaches: (1) the current size of the vesicle, (2) the total cross-sectional area of the magnetite crystals, and (3) the bubble size required for the aggregate to be neutrally buoyant. These approaches suggest a pre-eruptive bubble 300–850 μm in diameter, with a preferred value of 600–750 μm. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

12.
Gold species spontaneously deposited on pyrite and chalcopyrite, pyrrhotite, galena, sphalerite from HAuCl4 solutions at room temperature, as well as the state of the reacted mineral surfaces have been characterized using synchrotron radiation X-ray photoelectron spectroscopy (SR-XPS), scanning tunneling microscopy and tunneling spectroscopy (STM/STS). The deposition of silver from 10−4 M AgNO3 has been examined for comparison. Gold precipitates as metallic nanoparticles (NPs) from about 3 nm to 30 nm in diameter, which tends to aggregate forming larger particles, especially on pyrite. The Au 4f binding energies increase up to 1 eV with decreasing size of individual Au0 NPs, probably due to the temporal charging in the final state. Concurrently, a positive correlation between the tunneling current and the particle size was found in STS. Both these size effects were observed for unusually large, up to 20 nm Au particles. In contrast, silver deposited on the minerals as nanoparticles of semiconducting sulfide showed no shifts of photoelectron lines and different tunneling spectra.The quantity of gold deposited on pyrite and other minerals increased with time; it was lower for fracture surfaces and it grew if minerals were moderately pre-oxidized, while the preliminary leaching in Fe(III)-bearing media inhibited the following Au deposition. After the contact of polished minerals with 10−4 M solution (pH 1.5) for 10 min, the gold uptake changed in the order CuFeS2 > ZnS > PbS > FeAsS > FeS2 > Fe7S8. It was noticed that the open circuit (mixed) potentials of the minerals varied in approximately the same order, excepting chalcopyrite. We concluded that the potentials of minerals were largely determined by Fe(II)/Fe(III) couple, whereas the reduction of gold complexes had a minor effect. As a result, the deposition of gold, although it proceeded via the electrochemical mechanism, increased with decreasing potential. This suggests, in particular, that the accumulation of “invisible” gold in arsenian pyrites and arsenopyrite under hydrothermal conditions may be explained by the low electrochemical potentials but not structural relationships between As and Au in solids.  相似文献   

13.
Due to the widespread contamination of groundwater resources with arsenic (As), controls on As mobility have to be identified. In this study we focused on the distribution of As in the dissolved, colloidal and particulate size fraction of experimental solutions rich in ferric iron, dissolved organic matter (DOM) and As(V). Size fractions between <5 kDa and >0.2 μm were separated by filtration and their elemental composition was analyzed. A steady-state particle size distribution with stable element concentration in the different size classes was attained within 24 h. The presence of DOM partly inhibited the formation of large Fe-(oxy)hydroxide aggregates, thus stabilized Fe in complexed and colloidal form, when initially adjusted molar Fe/C ratios in solution were <0.1. Dissolved As concentrations and the quantity of As bound to colloids (<0.2 μm) increased in the presence of DOM as well. At intermediate Fe/C ratios of 0.02-0.1, a strong correlation between As and Fe concentration occurred in all size fractions (R2 = 0.989). At Fe/C ratios <0.02, As was mainly present in the dissolved size fraction. These observations indicate that As mobility increased in the presence of DOM due to (I) competition between As and organic molecules for sorption sites on Fe particles; and (II) due to a higher amount of As bound to more abundant Fe colloids or complexes <0.2 μm in size. The amount of As contained in the colloidal size fractions also depended strongly on the initial size of the humic substance, which was larger for purified humic acids than for natural river or soil porewater samples. Arsenic in the particle size fraction >0.2 μm additionally decreased in the order of pH 4 ? 6 > 8. The presence of DOM likely increases the mobility of As in iron rich waters undergoing oxidation, a finding that has to be considered in the investigation of organic-rich terrestrial and aquatic environments.  相似文献   

14.
It has been proposed that Archean tonalitic-trondhjemitic-granodioritic magmas (TTGs) formed by melting of mafic crust at high pressures. The residual mineralogy of the TTGs (either (garnet)-amphibolite or rutile-bearing eclogite) is believed to control the trace element budget of TTGs. In particular, ratios of high-field-strength elements (HFSE) can help to discriminate between the different residual lithologies. In order to place constraints on the source mineralogy of TTGs, we performed high-precision HFSE measurements by isotope dilution (Nb, Ta, Zr, Hf) together with Lu-Hf and Sm-Nd measurements on representative, ca. 3.85-2.8 Ga TTGs and related rock types from southern West Greenland, W-India and from the Superior Province. These measurements are complemented by major and trace element data for the TTGs. Texturally homogeneous early Archean (3.85-3.60 Ga old) and Mesoarchean (ca. 3.1-2.8 Ga old) TTGs have both low Ni (<11 ppm) and Cr contents (<20 ppm), indicating that there was little or no interaction with mantle peridotite during ascent. Ratios of Nb/Ta in juvenile Eoarchean TTGs range from ca. 7 to ca. 24, and in juvenile Mesoarchean TTGs from ca. 14 to ca. 27. Even higher Nb/Ta (14-42) were obtained for migmatitic TTGs and intra-crustal differentiates, most likely mirroring further fractionation of Nb from Ta as a consequence of partial melting, fluid infiltration and migmatisation. In the juvenile TTGs, positive correlations between Nb/Ta and Gd/Yb, La/Yb, Sr/Y, Zr/Sm and Zr/Nb are observed. These compositional arrays are best explained by melting of typical Isua tholeiites in both, the rutile-bearing eclogite stability field (>15 kbar, high Nb/Ta) and the garnet-amphibolite stability field (10-15 kbar, low Nb/Ta). With respect to the low end of Nb/Ta found for TTGs, there is currently some uncertainty between the available experimental datasets for amphibole. Independent of these uncertainties, the TTG compositions found here still require the presence of both endmember residues. A successful geological model for the TTGs therefore has to account for the co-occurrence of both low- and high-Nb/Ta TTGs within the same geologic terrane. An additional feature observed in the Eoarchean samples from Greenland is a systematic co-variation between Nb/Ta and initial εHf(t), which is best explained by a model where TTG-melting occured at progressively increasing pressures in a pile of tectonically thickened mafic crust. The elevated Nb/Ta in migmatitic TTGs and intra-crustal differentiates can shed further light on the role of intra-crustal differentiation processes in the global Nb/Ta cycle. Lower crustal melting processes at granulite facies conditions may generate high-Nb/Ta domains in the middle crust, whereas mid-crustal melting at amphibolite facies conditions may account for the low Nb/Ta generally observed in upper crustal rocks.  相似文献   

15.
The effect of three most important reagents for coal flotation namely sodium meta silicate, collector (kerosene) and frother (MIBC) was studied using 23 full factorial design. The regression models were developed using factorial experiment data to quantify the effect of sodium meta silicate, collector and frother and to predict grade and recovery of combustible material for different reagent conditions. The addition of sodium meta silicate increased the recovery without affecting the grade significantly. The MIBC addition reduce the surface tension at the liquid–vapor interface, which results in the production of finer bubble size distribution and thus improves flotation rates and recovery values. However, a finer bubble size distribution also increases water recovery, which results in a greater recovery of entrainable ash bearing particles and thus degradation of the product grade. The interaction between OH group of MIBC and hydrated mineral matter improves flotability of high ash coal particles and degrades the product grade further. The negative effect of kerosene and MIBC interaction on both grade and recovery could be due to the recovery of high ash coal particles in preference to low ash coal particles. The highest possible grade of product is 94.19% combustibles with 25.33% recovery. A product with 91.11% combustibles grade at 95.58% recovery was obtained at 0.1 g/kg sodium silicate, 0.4 g/kg collector and 0.075 g/kg frother from the coal fines tested.  相似文献   

16.
Smelting slags associated with base-metal vein deposits of the Sierra Almagrera area (SE Spain) show high concentrations of Ag (<5–180 ppm), As (12–750 ppm), Cu (45–183 ppm), Fe (3.2–29.8%), Pb (511–2150 ppm), Sb (22–620 ppm) and Zn (639–8600 ppm). The slags are mainly composed of quartz, fayalite, barite, melilite, celsian, pyrrhotite, magnetite, galena and Zn–Pb–Fe alloys. No glassy phases were detected. The following weathering-related secondary phases were found: jarosite–natrojarosite, cotunnite, cerussite, goethite, ferrihydrite, chalcanthite, copiapite, goslarite, halotrichite and szomolnokite. The weathering of slag dumps near the Mediterranean shoreline has contaminated the soils and groundwater, which has caused concentrations in groundwater to increase to 0.64 mg/L Cu, 40 mg/L Fe, 0.6 mg/L Mn, 7.6 mg/L Zn, 5.1 mg/L Pb and 19 μg/L As. The results of laboratory leach tests showed major solubilization of Al (0.89–12.6 mg/L), Cu (>2.0 mg/L), Fe (0.22–9.8 mg/L), Mn (0.85–40.2 mg/L), Ni (0.092–2.7 mg/L), Pb (>2.0 mg/L) and Zn (>2.5 mg/L), and mobilization of Ag (0.2–31 μg/L), As (5.2–31 μg/L), Cd (1.3–36.8 μg/L) and Hg (0.2–7 μg/L). The leachates were modeled using the numerical code PHREEQC. The results suggested the dissolution of fayalite, ferrihydrite, jarosite, pyrrhotite, goethite, anglesite, goslarite, chalcanthite and cotunnite. The presence of secondary phases in the slag dumps and contaminated soils may indicate the mobilization of metals and metalloids, and help to explain the sources of groundwater contamination.  相似文献   

17.
Despite its potential economic and environmental importance, the study of trace metals in supergene (secondary) Cu-sulfides has been seriously overlooked in the past decades. In this study, the concentration and mineralogical form of “invisible” precious metals (Ag, Au) and metalloids (As, Sb, Se, Te) in supergene digenite (Cu1.8S) from various Cu deposits in the Atacama Desert of northern Chile, the world’s premier Cu province, were determined in detail using a combination of microanalytical techniques. Secondary ion mass spectrometry (SIMS) and electron microprobe analyzer (EMPA) measurements reveal that, apart from hosting up to ∼11,000 ppm Ag, supergene digenite can incorporate up to part-per-million contents of Au (∼6 ppm) and associated metalloids such as As (∼300 ppm), Sb (∼60 ppm), Se (∼96 ppm) and Te (∼18 ppm). SIMS analyses of trace metals show that Ag and Au concentrations strongly correlate with As in supergene digenite, defining wedge-shaped zones in Ag-As and Au-As log-log spaces. SIMS depth profiling and high-resolution transmission electron microscopy (HRTEM) observations reveal that samples with anomalously high Ag/As (>∼30) and Au/As (>∼0.03) ratios plot above the wedge zones and contain nanoparticles of metallic Ag and Au, while samples with lower ratios contain Ag and Au that is structurally bound to the Cu-sulfide matrix. The Ag-Au-As relations reported in this study strongly suggest that the incorporation of precious metals in Cu-sulfides formed under supergene, low-temperature conditions respond to the incorporation of a minor component, in this case As. Therefore, As might play a significant role by increasing the solubility of Ag and Au in supergene digenite and controlling the formation and occurrence of Ag and Au nanoparticles. Considering the fact that processes of supergene enrichment in Cu deposits can be active from tens of millions of years (e.g. Atacama Desert), we conclude that supergene digenite may play a previously unforeseen role in scavenging precious metals from undersaturated (or locally slightly supersaturated) solutions in near-surface environments.  相似文献   

18.
Orogenic gold-bearing quartz veins in the middle Tertiary Bullendale Fault Zone, New Zealand were mined historically for coarse gold in a narrow zone (ca. 5 m thick). However, recent drilling has revealed a broad hydrothermal alteration zone extending into the host schist, in which disseminated sulphide and gold mineralisation has occurred. The evidence of alteration is first seen over 150 m across strike from the fault zone, and the best-developed alteration halo is about 50 m wide. The extent and intensity of alteration is strongly controlled by local structures that developed during regional Tertiary kink folding of the pervasively foliated and fissile metasedimentary schist host. The earliest structures are foliation-parallel microshears (micron to millimeter scale) formed during flexural-slip folding. Later, but related, structures are predominantly normal faults and associated shear zones that have formed extensional sites during the regional folding event. All these structures facilitated hydrothermal fluid penetration and rock alteration, with localised vein formation and brecciation. Where fluid has followed structures, metamorphic chlorite, phengite, and titanite have been altered to hydrothermal ankerite, rutile, and muscovite or kaolinite. Ankerite with Fe/(Fe + Mg) < 0.4 formed in host rocks with Fe/(Fe + Mg) of 0.6, and iron released by ankerite alteration possibly formed pyrite and arsenopyrite that host disseminated gold. Fault zones were extensively silicified and veined with quartz, albite, sulphides, and gold. Host rocks have wide compositional variations because of centimeter-scale metamorphic segregation. However, the alteration halo is characterised by elevated CO2 and S, as measured by loss-on-ignition (doubled to ca. 6 wt.%), elevated As (100–10,000 ppm), and weakly elevated Sb (up to 14 ppm). Strontium is elevated and Ba depleted in many altered rocks, so Sr/Ba ratio increases from < 1 (host rocks) to > 3 in the most altered and silicified rocks. Many altered and mineralised rocks have low Sr/Ba (< 0.5) as well. The subtle geochemical signature is not useful as a vector to ore because of the strong microstructural control on alteration. Likewise, there is no evidence for spatial mineralogical zonation across the alteration halo, although the most intense alteration is centred on the main fault zone, and intensity of alteration is controlled by microstructures at all scales. As documented in previous studies, hydrothermal alteration haloes enlarge the exploration target for some orogenic gold deposits, and may include disseminated gold, as in this Bullendale example.  相似文献   

19.
The present study illustrates the interest of using the elastic recoil detection analysis (ERDA) method to characterize any geological sample matrix with respect to hydrogen. ERDA is combined with Rutherford back scattering (RBS) and particle induced X-ray emission (PIXE), allowing the simultaneous characterization of the matrix with respect to major and trace elements (Z > 15). Analyses are performed by mapping of a 4 × 16 μm2 incident beam of 4He+ on large areas (50 × 200 μm2). The method is almost not destructive and requires no calibration with respect to well known hydrous samples. Hydrous and nominally anhydrous phases in contact with each other in the same sample may both be characterized. The depth of the analyses is limited to several μm beneath the surface, allowing tiny samples to be investigated, provided their sizes are larger than the incident beam. Our setup has been improved in order to allow H determination on a micrometric scale with a 5-15% relative uncertainty and a detection limit of 94 wt ppm H2O. We present multi-elemental mappings on a large panel of samples: (1) natural and analogue synthetic glasses from Stromboli volcano (0.44-4.59 wt% H2O), natural rhyolitic glasses (1466-1616 wt ppm H2O); (2) magmatic rhyolitic melt inclusions from Guadeloupe Island (4.37-5.47 wt% H2O) and their quartz host crystal (2020 ± 230 wt ppm H2O); (3) nominally anhydrous natural (82-260 wt ppm H2O) and experimentally hydrated (240-790 wt ppm H2O) olivines; natural clinopyroxenes (159-716 wt ppm H2O); natural orthopyroxenes (201-452 wt ppm H2O); a natural garnet (90 wt ppm H2O). Results show that ERDA is a strong and accurate reference method that can be used to characterize geological sample from various matrix compositions from high to low water contents. It can be used to calibrate other methods of microanalysis such as Fourier Transform Infrared Spectroscopy (FTIR) or secondary ion mass spectrometry (SIMS).  相似文献   

20.
At 1,175°C-1 bar, muscovite in natural granite powders is completely transformed after 5 min. Due to the overlapping of several processes such as dehydroxylation, mineralogical transformations, collapse and sintering of transformed lamellae, a few parts per thousand of H2O vapor are trapped, generating bubbles in muscovite pseudomorphs. For short durations (5–40 min), the crystallographic properties of the precursor muscovite control the geometry of the bubbles that may be compared to thick disks with a rounded shape in basal sections and an elongated shape in lateral section, parallel to the former cleavage planes of muscovite. With longer durations the bubbles change from thick disks to spheres, which can be explained by the release of constraints perpendicular to basal planes upon growth of the high temperature Si–Al oxides. With time, the number of bubbles decreases while the bubble size and the porosity of the pseudomorphs increase. Bubble behavior was analyzed in terms of ripening, shape transformations and coalescence.  相似文献   

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