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1.
The leaching behaviour of fly ash from a Co smelter situated in the Zambian Copperbelt was studied as a function of pH (5–12) using the pH-static leaching test (CEN/TS 14997). Various experimental time intervals (48 h and 168 h) were evaluated. The leaching results were combined with the ORCHESTRA modelling framework and a detailed mineralogical investigation was performed on the original FA and leached solid residues. The largest amounts of Co, Cu, Pb and Zn were leached at pH 5, generally with the lowest concentrations between pH 9 and 11 and slightly increased concentrations at pH 12. For most elements, the released concentrations were very similar after 48 h and 168 h, indicating near-equilibrium conditions in the system. Calcite, clinopyroxenes, quartz and amorphous phases predominated in the fly ash. Various metallic sulfides, alloys and the presence of Cu, Co and Zn in silicates and glass were detected using SEM/EDS and/or TEM/EDS. The leaching of metals was mainly attributed to the dissolution of metallic particles. Partial dissolution of silicate and glass fractions was assumed to significantly influence the release of Ca, Mg, Fe, K, Al and Si as well as Cu, Co and Zn. The formation of illite was suggested by the ORCHESTRA modelling to be one of the main solubility-controlling phases for major elements, whereas Co and Zn were controlled by CoO and zincite, respectively. Sorption of metals on hydrous ferric oxides was assumed to be an important attenuation mechanism, especially for the release of Pb and Cu. However, there is a high risk of Co, Cu, Pb and Zn mobility in the acidic soils around the smelter facility. Therefore, potential local options for “stabilisation” of the fly ash were evaluated on the basis of the modelling results using the PHREEQC code.  相似文献   

2.
Remediation of 56 ML of acidic, contaminant-laden Baal Gammon mine pit water was undertaken using in situ hydrotalcite formation. The pit water composition was modified via the addition of MgCl2·6H2O to form a 2.5:1 M2+:M3+ metal ion ratio followed by the addition of NaOH to increase the pH 10 to induce spontaneous hydrotalcite precipitation. As a result of the in situ hydrotalcite precipitation a broad spectrum of elements of environmental concern including Al, Cd, Co, Cr, Cu, Fe, In, Mn, Mo, Ni, V and Zn were removed from solution. Significantly, an ore grade hydrotalcite precipitate containing Cu (8.0 ± 1.0%) and Zn (3.9 ± 0.5%) was produced directly from the mine pit water column allowing for potential recovery of valuable metals to offset remediation costs. The final water quality produced after in situ remediation was of a simple Na–Cl–SO4 type.  相似文献   

3.
《Applied Geochemistry》2007,22(4):760-777
Ochreous precipitate and water samples were collected from the surroundings of seven closed sulphide mines in Finland. In the Hammaslahti Zn–Cu–Au mine, Otravaara pyrite mine and Paroistenjärvi Cu–W–As mine, the collection was repeated in different seasons to study mineralogical and geochemical variations of precipitates. The sampling was done in 1999–2002 from the ditches and drainage ponds of the tailings and waste rock piles that are susceptible to seasonal changes. Mineralogy of the precipitates was evaluated by X-ray diffraction (XRD) and infrared spectroscopy (IR), and precipitate geochemistry was examined by selective extractions. Schwertmannite (Fe8O8(OH)6SO4) was the most typical Fe hydroxide mineral found. Goethite was almost as common as schwertmannite, was often poorly ordered, and contained up to 10 wt.% of SO4. Goethite and schwertmannite were commonly found as mixtures, and they occurred in similar pH and SO4 concentrations. Ferrihydrite (nominally Fe5HO8 · 4H2O) was typically found in areas not influenced by acid mine drainage, and also in acid mine waters with high organic matter or As content. Jarosite (KFe3(SO4)2(OH)6) was found only in one site. In addition, some gypsum (CaSO4 · 2H2O) and aluminous sulphate precipitates (presumably basaluminite, Al4(SO4)(OH)10 · 5H2O) were identified. Selective extractions showed that acid extracts Fetot/Stot-ratios of schwertmannite and goethite samples were similar, but the ratio of oxalate-extractable to total Fe, Feox/Fetot, of goethite samples were lower than those of the schwertmannite samples. Only Al, Si and As were bound to precipitates in substantial amounts, up to several wt.%. In schwertmannites and goethites, Al, Cu, Co, Mn and Zn were mostly structural, substituting for Fe in an Fe oxyhydroxide structure or bound to surface adsorption sites in pores limited by diffusion. In ferrihydrites, heavy metals were also partly bound in adsorbed form dissolving in acid ammonium acetate. Ferrihydrites and goethites were more enriched in Co, Mn and Zn than schwertmannites, but schwertmannites and ferrihydrites were more enriched in As than goethites. Mineralogical and geochemical evidence showed that in the spring, after the snowmelt, the acid mine drainage precipitates were predominantly schwertmannite, and were partly transformed during warm summer months to goethite. The phase transformation of precipitates was followed by a decrease in pH values and increase in SO4 concentrations of waters. Adsorbed As retarded the phase transformation.  相似文献   

4.
The Loulo–Gounkoto complex in the Kédougou–Kéniéba Inlier hosts three multi-million ounce orogenic gold deposits, situated along the Senegal–Mali Shear Zone. This west Malian gold belt represents the largest West African orogenic gold district outside Ghana. The Gounkoto deposit is hosted to the south of the Gara and Yalea gold mines in the Kofi Series metasedimentary rocks. The ore body is structurally controlled and is characterised by sodic and phyllic alteration, As- and Fe-rich ore assemblages, with abundant magnetite, and overall enrichment in Fe–As–Cu–Au–Ag–W–Ni–Co–REE + minor Te–Pb–Se–Cd. Fluid inclusion analysis indicates that the deposit formed at P–T conditions of approximately 1.4 kbar and 340 °C and that two end member fluids were involved in mineralisation: (1) a moderate temperature (315–340 °C), low salinity (< 10 wt.% NaCl equiv.), low density (≤ 1 g·cm− 3), H2O–CO2–NaCl–H2S ± N2–CH4 fluid; (2) a high temperature (up to 445 °C), hypersaline (~ 40 wt.% NaCl equiv.), high density (~ 1.3 g·cm− 3), H2O–CO2–NaCl ± FeCl2 fluid. Partial mixing of these fluids within the Jog Zone at Gounkoto enhanced phase separation in the aqueo-carbonic fluid and acted as a precipitation mechanism for Au. These findings demonstrate the widespread, if heterogeneously distributed, nature of fluid mixing as an ore forming process in the Loulo–Gounkoto complex, operating over at least a 30 km strike length of the shear zone. Stable isotope analyses of ore components at Gounkoto indicate a dominant metamorphic source for H2O, H2S and CO2, and by extension Au. It thus can be reasoned that both the aqueo-carbonic and the hypersaline fluid at Gounkoto are of metamorphic origin and that the high levels of salinity in the brine are likely derived from evaporite dissolution.  相似文献   

5.
《Applied Geochemistry》2006,21(11):1969-1985
Gossan Creek, a headwater stream in the SE Upsalquitch River watershed in New Brunswick, Canada, contains elevated concentrations of total Hg (HgT up to 60 μg/L). Aqueous geochemical investigations of the shallow groundwater at the headwaters of the creek confirm that the source of Hg is a contaminated groundwater plume (neutral pH with Hg and Cl concentrations up to 150 μg/L and 20 mg/L, respectively), originating from the Murray Brook mine tailings, that discharges at the headwaters of the creek. The discharge area of the contaminant plume was partially delineated based on elevated pH and Cl concentrations in the groundwater. The local groundwater outside of the plume contains much lower concentrations of Hg and Cl (<0.1 μg/L and 3.8 mg/L, respectively) and displays the chemical characteristics of an acid-sulfate weathering system, with low pH (4.1–5.5) and elevated concentrations of Cu, Zn, Pb and SO4 (up to 5400 μg Cu/L, 8700 μg Zn/L, 70 μg Pb/L and 330 mg SO4/L), derived from oxidation of sulfide minerals in the Murray Brook volcanogenic massive sulfide deposit and surrounding bedrock. The HgT mass loads measured at various hydrologic control points along the stream system indicate that 95–99% of the dissolved HgT is attenuated in the first 3–4 km from the source. Analyses of creek bed sediments for Au, Ag, Cu, Zn, Pb and Hg indicate that these metals have partitioned strongly to the sediments. Mineralogical investigations of the contaminated sediments using analytical scanning electron microscopy (SEM), transmission electron microscopy (TEM) and scanning transmission electron microscopy (STEM), reveal discrete particles (<1–2 μm) of metacinnabar (HgS), mixed Au–Ag–Hg amalgam, Cu sulfide and Ag sulfide.  相似文献   

6.
《Applied Geochemistry》2006,21(7):1216-1225
The aim of the study was to determine whether the application of bulk industrial chemicals (potassium permanganate and water-soluble phosphate fertilizer) to partly oxidized, polyminerallic mine wastes can inhibit sulfide oxidation, and metal and metalloid mobility. The acid producing waste rocks were metal (Pb, Zn, Cu) and metalloid (As, Sb) rich and consisted of major quartz, dickite, illite, and sulfide minerals (e.g., galena, chalcopyrite, tetrahedrite, sphalerite, pyrite, arsenopyrite), as well as minor to trace amounts of pre- and post-mining oxidation products (e.g., hydrated Fe, Cu, Pb, and alkali mineral salts). SEM-EDS observations of treated waste material showed that metal, metal–alkali, and alkali phosphate coatings developed on all sulfides. The abundance of phosphate phases was dependant on the fertilizer type and the availability of metal and alkali cations in solution. In turn, the release of cations was dependent on the amount of sulfide oxidation induced by KMnO4 during the experiment and the dissolution of soluble sulfates. Mn, Ca, Fe, and Pb phosphates remained stable during H2O2 leaching, preventing acid generation and metal release. In contrast, the lack of complete phosphate coating on arsenopyrite allowed oxidation and leaching of As to proceed. The mobilized As did not form phosphate phases and consequently, As displayed the greatest release from the coated waste. Thus, the application of KMnO4 and the water-soluble phosphate fertilizer Trifos (Ca(H2PO4)2) to partly oxidized, polyminerallic mine wastes suppresses sulfide oxidation and is most effective in inhibiting Cu, Pb, and Zn (Sb) release. However, the technique appears ineffective in suppressing oxidation of arsenopyrite and preventing As leaching.  相似文献   

7.
Chalcopyrite, CuFeS2, is an important source of copper and is recovered from ore by the flotation process. Chalcopyrite is commonly associated with other metal sulfides, e.g. bornite, Cu5FeS4. In this study the effect of bornite on the oxidation and leaching of chalcopyrite has been investigated by probing the surface evolution of pure chalcopyrite, bornite, and heterogeneous samples containing both chalcopyrite and bornite using Synchrotron X-ray Photoelectron Spectroscopy (SXPS). Samples were freshly fractured in a N2 atmosphere and the resulting surfaces were oxidised in pH 9 KOH for 30 min or leached in pH 1 HCl for 2 h before being transferred into vacuum without leaving the N2 atmosphere. Analysis of the chalcopyrite region of each sample indicates that exposure to pH 9 for 30 min when bornite is present results in a decreased concentration of hydrophobic polysulfide species (from 43% to 36% of the total S 2p spectrum). In addition to this decrease in hydrophobic species, there is an increase in the amount of hydrophilic sulfate on the surface, from trace amounts to 3%. For those samples leached at pH 1 there was a small decrease in the amount of polysulfide species (43% to 39%), but also a slight increase in disulfide species (16% to 19%) indicating an alteration to the oxidation process at low pH in the presence of bornite.  相似文献   

8.
As, Cd, Cr, Cu, U, and Zn in Aqaba and Eshidiya phosphogypsum showed relative uniformity in particle size presented by coarse (>0.212 mm); medium (0.212–0.053 mm); and fine (<0.053 mm) in the stacks by age of deposition. Jordan phosphogypsum contains low concentrations of As, Cd, Cr, Cu, U, and Zn compared to those reported worldwide. The bioavailability and mobility of trace metals were estimated using aqua regia leaching experiments. Leaching results have shown that around 3% of the As, 1% of the Cd, 5% of the Cr, 9% of the Cu, 4% of the U, and 3% of the Zn are transferred to the surrounding aquatic environment and/or soils. Mobility of trace metals in phosphogypsum was classified into three degrees: elements with high mobility were Cu and U; those with moderate mobility were As and Zn; and those with low mobility were Cd and Cr. It can be concluded that As, Cd, Cr, Cu, U, and Zn were not only uniformly distributed in the stack, but they are not leached from the phosphogypsum stacks in any significant amount, and then they are not easily transferred to the surrounding aquatic environment and/or soils.  相似文献   

9.
The Linghou deposit, located near Hangzhou City of Zhejiang Province, eastern China, is a medium-sized polymetallic sulfide deposit associated with granitic intrusion. This deposit is structurally and lithologically controlled and commonly characterized by ore veins or irregular ore lenses. In this deposit, two mineralization events were identified, of which the former produced the Cu–Au–Ag orebodies, while the latter formed Pb–Zn–Cu orebodies. Silicification and calc-silicate (skarn type), phyllic, and carbonate alternation are four principal types of hydrothermal alteration. The early Cu–Au–Ag and late Pb–Zn–Cu mineralizations are characterized by quartz ± sericite + pyrite + chalcopyrite + bornite ± Au–Ag minerals ± magnetite ± molybdenite and calcite + dolomite + sphalerite + pyrite + chalcopyrite + galena, respectively. Calcite clusters and calcite ± quartz vein are formed during the late hydrothermal stage.The NaCl–H2O–CO2 system fluid, coexisting with NaCl–H2O system fluid and showing the similar homogenization temperatures (385 °C and 356 °C, respectively) and different salinities (16.89–21.68 wt.% NaCl eqv. and 7.70–15.53 wt.% NaCl eqv.), suggests that fluid immiscibility occurred during the Cu–Au–Ag mineralization stage and might have given rise to the ore-metal precipitation. The ore-forming fluid of the Pb–Zn–Cu mineralization mainly belongs to the NaCl–H2O–CO2 system of high temperature (~ 401 °C) and mid-high salinity (10.79 wt.% NaCl eqv.).Fluids trapped in the quartz-chalcopyrite vein, Cu–Au–Ag ores, Pb–Zn–Cu ores and calcite clusters yielded δ18OH2O and δD values varying from 5.54‰ to 13.11‰ and from − 71.8‰ to − 105.1‰, respectively, indicating that magmatic fluids may have played an important role in two mineralization events. The δ13CPDB values of the calcite change from − 2.78‰ to − 4.63‰, indicating that the CO32 − or CO2 in the ore-forming fluid of the Pb–Zn–Cu mineralization was mainly sourced from the magmatic system, although dissolution of minor marine carbonate may have also occurred during the ore-forming processes. The sulfide minerals have homogeneous lead isotopic compositions with 206Pb/204Pb ranging from 17.958 to 18.587, 207Pb/204Pb ranging from 15.549 to 15.701, and 208Pb/204Pb ranging from 37.976 to 39.052, indicating that metallic elements of the Linghou deposit came from a mixed source involving mantle and crustal components.Based on geological evidence, fluid inclusions, and H–O–C–S–Pb isotopic data, the Linghou polymetallic deposit is interpreted as a high-temperature, skarn-carbonate replacement type. Two types of mineralization are both related to the magmatic–hydrothermal system, with the Cu–Au–Ag mineralization having a close relationship with granodiorite.  相似文献   

10.
This paper contributes to the understanding of the genesis of epigenetic, hypogene BIF-hosted iron deposits situated in the eastern part of Ukrainian Shield. It presents new data from the Krivoy Rog iron mining district (Skelevatske–Magnetitove deposit, Frunze underground mine and Balka Severnaya Krasnaya outcrop) and focuses on the investigation of ore genesis through application of fluid inclusion petrography, microthermometry, Raman spectroscopy and baro-acoustic decrepitation of fluid inclusions. The study investigates inclusions preserved in quartz and magnetite associated with the low-grade iron ores (31–37% Fe) and iron-rich quartzites (38–45% Fe) of the Saksaganskaya Suite, as well as magnetite from the locally named high-grade iron ores (52–56% Fe). These high-grade ores resulted from alteration of iron quartzites in the Saksaganskiy thrust footwall (Saksaganskiy tectonic block) and were a precursor to supergene martite, high-grade ores (60–70% Fe). Based on the new data two stages of iron ore formation (metamorphic and metasomatic) are proposed.The metamorphic stage, resulting in formation of quartz veins within the low-grade iron ore and iron-rich quartzites, involved fluids of four different compositions: CO2-rich, H2O, H2O–CO2(± N2–CH4)–NaCl(± NaHCO3) and H2O–CO2(± N2–CH4)–NaCl. The salinities of these fluids were relatively low (up to 7 mass% NaCl equiv.) as these fluids were derived from dehydration and decarbonation of the BIF rocks, however the origin of the nahcolite (NaHCO3) remains unresolved. The minimum P–T conditions for the formation of these veins, inferred from microthermometry are Tmin = 219–246 °C and Pmin = 130–158 MPa. The baro-acoustic decrepitation analyses of magnetite bands indicated that the low-grade iron ore from the Skelevatske–Magnetitove deposit was metamorphosed at T = ~ 530 °C.The metasomatic stage post-dated and partially overlapped the metamorphic stage and led to the upgrade of iron quartzites to the high-grade iron ores. The genesis of these ores, which are located in the Saksaganskiy tectonic block (Saksaganskiy ore field), and the factors controlling iron ore-forming processes are highly controversial. According to the study of quartz-hosted fluid inclusions from the thrust zone the metasomatic stage involved at least three different episodes of the fluid flow, simultaneous with thrusting and deformation. During the 1st episode three types of fluids were introduced: CO2–CH4–N2(± C), CO2(± N2–CH4) and low salinity H2O–N2–CH4–NaCl (6.38–7.1 mass% NaCl equiv.). The 2nd episode included expulsion of the aqueous fluids H2O–N2–CH4–NaCl(± CO2, ± C) of moderate salinities (15.22–16.76 mass% NaCl equiv.), whereas the 3rd event involved high salinity fluids H2O–NaCl(± C) (20–35 mass% NaCl equiv.). The fluids most probably interacted with country rocks (e.g. schists) supplying them with CH4 and N2. The high salinity fluids were most likely either magmatic–hydrothermal fluids derived from the Saksaganskiy igneous body or heated basinal brines, and they may have caused pervasive leaching of Fe from metavolcanic and/or the BIF rocks. The baro-acoustic decrepitation analyses of magnetite comprising the high-grade iron ore showed formation T = ~ 430–500 °C. The fluid inclusion data suggest that the upgrade to high-grade Fe ores might be a result of the Krivoy Rog BIF alteration by multiple flows of structurally controlled, metamorphic and magmatic–hydrothermal fluids or heated basinal brines.  相似文献   

11.
Huogeqi is a shear zone-hosted epigenetic deposit within the greenschist-amphibolite facies of the Mesoproterozoic Langshan Group in the Langshan district on the northern margin of the North China Craton (NCC). Copper mineralization in the Huogeqi deposit was formed in two stages: a main-stage controlled by the shear zone and characterized by brittle-ductile ore-forming structures and a lower greenschist facies mineral assemblage, and a late stage characterized by open space-filling textures and low-temperature minerals. Based on microthermometric and Raman microprobe analysis, the main-stage Cu-bearing fluid was mesothermal, low-salinity and H2O–CH4-dominant, and was generated by an interaction between a deep-crustal metamorphic fluid and graphite-bearing host rocks. This interaction resulted in a more CH4-rich fluid, which was more amenable to be immiscible. We showed that immiscibility of the H2O–CH4 fluid occurred due to temperature decrease, prior to the main-stage Cu mineralization; Cu was finally precipitated from the resultant H2O-rich aqueous fluid. Main-stage Cu mineralization temperature was obtained using various methods: 310–370 °C by intersection of isochors of coexistent CH4 and aqueous inclusions; 364 ± 41 °C on average by pressure correction of the homogenization temperatures of aqueous inclusions; and 362 ± 26 °C using the chlorite geothermometer. Pressure during Cu-deposition fluctuated between lithostatic and hydrostatic at depths of ca. 10–12 km, but it seemingly had no effect on the mineralization process. The late-stage Cu-bearing fluid was a low temperature, low salinity, H2O of meteoric origin.  相似文献   

12.
The interaction of groundwater with cement in a geological disposal facility (GDF) for intermediate level radioactive waste will produce a high pH leachate plume. Such a plume may alter the physical and chemical properties of the GDF host rock. However, the geochemical and mineralogical processes which may occur in such systems over timescales relevant for geological disposal remain unclear. This study has extended the timescale for laboratory experiments and shown that, after 15 years two distinct phases of reaction may occur during alteration of a dolomite-rich rock at high pH. In these experiments the dissolution of primary silicate minerals and the formation of secondary calcium silicate hydrate (C–S–H) phases containing varying amounts of aluminium and potassium (C–(A)–(K)–S–H) during the early stages of reaction (up to 15 months) have been superseded as the systems have evolved. After 15 years significant dedolomitisation (MgCa(CO3)2 + 2OH− → Mg(OH)2 + CaCO3 + CO32−(aq)) has led to the formation of magnesium silicates, such as saponite and talc, containing variable amounts of aluminium and potassium (Mg–(Al)–(K)–silicates), and calcite at the expense of the early-formed C–(A)–(K)–S–H phases. This occured in high pH solutions representative of two different periods of cement leachate evolution with little difference in the alteration processes in either a KOH and NaOH or a Ca(OH)2 dominated solution but a greater extent of alteration in the higher pH KOH/NaOH leachate. The high pH alteration of the rock over 15 years also increased the rock’s sorption capacity for U(VI). The results of this study provide a detailed insight into the longer term reactions occurring during the interaction of cement leachate and dolomite-rich rock in the geosphere. These processes have the potential to impact on radionuclide transport from a geodisposal facility and are therefore important in underpinning any safety case for geological disposal.  相似文献   

13.
《Chemical Geology》2006,225(3-4):256-265
SeO42− ions can substitute for sulphate in the gypsum structure. In this work crystals of different Ca(SO4,SeO4)·2H2O solid solutions were precipitated by mixing a CaCl2 solution with solutions containing different ratios of Na2SO4 and Na2SeO4. The compositions of the precipitates were analysed by EDS and the cell parameters were determined by X-ray powder diffraction. Moreover, a comparative study on dehydration behaviour of selenate rich and sulfate rich Ca(SO4,SeO4)·2H2O solid solutions was carried out by thermogravimetry.The experimental results show that the Ca(SO4,SeO4)·2H2O solid solution presents a symmetric miscibility gap for compositions ranging from XCaSO4·2H2O = 0.23 to XCaSO4·2H2O = 0.77. By considering a regular solution model a Guggenheim parameter a0 = 2.238 was calculated. The solid phase activity coefficients obtained with this parameter were used to calculate a Lippmann diagram for the system Ca(SO4,SeO4)·2H2O–H2O.  相似文献   

14.
《Applied Geochemistry》2005,20(10):1941-1964
The pH, alkalinity, and acidity of mine drainage and associated waters can be misinterpreted because of the chemical instability of samples and possible misunderstandings of standard analytical method results. Synthetic and field samples of mine drainage having various initial pH values and concentrations of dissolved metals and alkalinity were titrated by several methods, and the results were compared to alkalinity and acidity calculated based on dissolved solutes. The pH, alkalinity, and acidity were compared between fresh, unoxidized and aged, oxidized samples.Data for Pennsylvania coal mine drainage indicates that the pH of fresh samples was predominantly acidic (pH 2.5–4) or near neutral (pH 6–7); ≈ 25% of the samples had pH values between 5 and 6. Following oxidation, no samples had pH values between 5 and 6.The Standard Method Alkalinity titration is constrained to yield values >0. Most calculated and measured alkalinities for samples with positive alkalinities were in close agreement. However, for low-pH samples, the calculated alkalinity can be negative due to negative contributions by dissolved metals that may oxidize and hydrolyze.The Standard Method hot peroxide treatment titration for acidity determination (Hot Acidity) accurately indicates the potential for pH to decrease to acidic values after complete degassing of CO2 and oxidation of Fe and Mn, and it indicates either the excess alkalinity or that required for neutralization of the sample. The Hot Acidity directly measures net acidity (= −net alkalinity). Samples that had near-neutral pH after oxidation had negative Hot Acidity; samples that had pH < 6.3 after oxidation had positive Hot Acidity. Samples with similar pH values before oxidation had dissimilar Hot Acidities due to variations in their alkalinities and dissolved Fe, Mn, and Al concentrations. Hot Acidity was approximately equal to net acidity calculated based on initial pH and dissolved concentrations of Fe, Mn, and Al minus the initial alkalinity. Acidity calculated from the pH and dissolved metals concentrations, assuming equivalents of 2 per mole of Fe and Mn and 3 per mole of Al, was equivalent to that calculated based on complete aqueous speciation of FeII/FeIII. Despite changes in the pH, alkalinity, and metals concentrations, the Hot Acidities were comparable for fresh and most aged samples.A meaningful “net” acidity can be determined from a measured Hot Acidity or by calculation from the pH, alkalinity, and dissolved metals concentrations. The use of net alkalinity = (Alkalinitymeasured − Hot Aciditymeasured) to design mine drainage treatment can lead to systems with insufficient Alkalinity to neutralize metal and H+ acidity and is not recommended. The use of net alkalinity = −Hot Acidity titration is recommended for the planning of mine drainage treatment. The use of net alkalinity = (Alkalinitymeasured − Aciditycalculated) is recommended with some cautions.  相似文献   

15.
Several occurrences of gold-bearing quartz veins are situated along the east–northeast-trending Barramiya–Um Salatit ophiolitic belt in the central Eastern Desert of Egypt. In the Barramiya mine, gold mineralization within carbonaceous, listvenized serpentinite and adjacent to post-tectonic granite stocks points toward a significant role of listvenitization in the ore genesis. The mineralization is related to quartz and quartz–carbonate lodes in silicified/carbonatized wallrocks. Ore minerals, disseminated in the quartz veins and adjacent wallrocks are mainly arsenopyrite, pyrite and trace amounts of chalcopyrite, sphalerite, tetrahedrite, pyrrhotite, galena, gersdorffite and gold. Partial to complete replacement of arsenopyrite by pyrite and/or marcasite is common. Other secondary phases include covellite and goethite. Native gold and gold–silver alloy occur as tiny grains along micro-fractures in the quartz veins. However, the bulk mineralization can be attributed to auriferous arsenopyrite and arsenic-bearing pyrite (with hundreds of ppms of refractory Au), as evident by electron microprobe and LA-ICP-MS analyses.The mineralized quartz veins are characterized by abundant carbonic (CO2 ± CH4 ± H2O) and aqueous-carbonic (H2O–NaCl–CO2 ± CH4) inclusions along intragranular trails, whereas aqueous inclusions (H2O–NaCl ± CO2) are common in secondary sites. Based on the fluid inclusions data combined with thermometry of the auriferous arsenopyrite, the pressure–temperature conditions of the Barramiya gold mineralization range from 1.3 to 2.4 kbar at 325–370 °C, consistent with mesothermal conditions. Based on the measured δ34S values of pyrite and arsenopyrite intimately associated with gold, the calculated δ34SΣs values suggest that circulating magmatic, dilute aqueous-carbonic fluids leached gold and isotopically light sulfur from the ophiolitic sequence. As the ore fluids infiltrated into the sheared listvenite rocks, a sharp decrease in the fluid fO2 via interaction with the carbonaceous wallrocks triggered gold deposition in structurally favorable sites.  相似文献   

16.
Significant amounts of sulfuric acid (H2SO4) rich saline water can be produced by the oxidation of sulfide minerals contained in inland acid sulfate soils (IASS). In the absence of carbonate minerals, the dissolution of phyllosilicate minerals is one of very few processes that can provide long-term acid neutralisation. It is therefore important to understand the acid dissolution behavior of naturally occurring clay minerals from IASS under saline–acidic solutions. The objective of this study was to investigate the dissolution of a natural clay-rich sample under saline–acidic conditions (pH 1–4; ionic strengths = 0.01 and 0.25 M; 25 °C) and over a range of temperatures (25–45 °C; pH 1 and pH 4). The clay-rich sample referred to as Bottle Bend clay (BB clay) used was from an IASS (Bottle Bend lagoon) in south-western New South Wales (Australia) and contained smectite (40%), illite (27%), kaolinite (26%) and quartz (6%). Acid dissolution of the BB clay was initially rapid, as indicated by the fast release of cations (Si, Al, K, Fe, Mg). Relatively higher Al (pH 4) and K (pH 2–4) release was obtained from BB clay dissolution in higher ionic strength solutions compared to the lower ionic strength solutions. The steady state dissolution rate (as determined from Si, Al and Fe release rates; RSi, RAl, RFe) increased with decreasing solution pH and increasing temperature. For example, the highest log RSi value was obtained at pH 1 and 45 °C (−9.07 mol g−1 s−1), while the lowest log RSi value was obtained at pH 4 and 25 °C (−11.20 mol g−1 s−1). A comparison of these results with pure mineral dissolution rates from the literature suggests that the BB clay dissolved at a much faster rate compared to the pure mineral samples. Apparent activation energies calculated for the clay sample varied over the range 76.6 kJ mol−1 (pH 1) to 37.7 kJ mol−1 (pH 4) which compare very well with the activation energy values for acidic dissolution of monomineralic samples e.g. montmorillonite from previous studies. The acid neutralisation capacity (ANC) of the clay sample was calculated from the release of all structural cations except Si (i.e. Al, Fe, K, Mg). According to these calculations an ANC of 1.11 kg H2SO4/tonne clay/day was provided by clay dissolution at pH 1 (I = 0.25 M, 25 °C) compared to an ANC of 0.21 kg H2SO4/tonne clay/day at pH 4 (I = 0.25 M, 25 °C). The highest ANC of 6.91 kg H2SO4/tonne clay/day was provided by clay dissolution at pH 1 and at 45 °C (I = 0.25 M), which is more than three times higher than the ANC provided under the similar solution conditions at 25 °C. In wetlands with little solid phase buffering available apart from clay minerals, it is imperative to consider the potential ANC provided by the dissolution of abundantly occurring phyllosilicate minerals in devising rehabilitation schemes.  相似文献   

17.
The components and concentrations of metals in street dust are indictors of environmental pollution. To explore the pollution levels of Cd, Cr, Cu, Mn, Ni and Pb in street dust and their spatial distribution characteristics, 220 dust samples were collected in a grid pattern from urban street surfaces in Beijing. Multivariate statistics and spatial analyses were adopted to investigate the associations between metals and to identify their pollution patterns. In comparison with the soil background values, elevated metal concentrations were found, except those for Mn and Ni. The results of the geo-accumulation index (Igeo) and the potential ecological risk index (Eri) of the metals revealed the following orders: Cd > Cu > Cr > Pb > Ni > Mn and Cd > Cu > Pb > Cr > Ni. Levels of Igeo ranging from 0 to 5 were found and about 80% of the samples were below the moderately polluted level. The Eri values of single elements were within the low ecological risk level in most sampling sites. Most of the metals in the street dust of Beijing were statistically significantly correlated. It is hard to clearly identify the sources of each metal in the street dust since local environments are very complex. Cadmium, Cu, Cr, Mn and Pb showed medium spatial autocorrelations within the sampling region. Similar spatial distribution patterns were observed for Cu, Cr and Pb, and these metals had relatively high spatial variabilities and were enriched in the center of the city with several peaks scattered in the suburbs. Metal pollution anomalies were identified by using cluster and outlier analyses. Locations identified as clusters with high values indicated non-point source pollution, while locations identified as outliers with high values indicated point source pollution. Traffic, construction, and other human activities influenced these high values. In addition, the locations identified as outliers with low values in urban areas might benefit from less transportation and better management.  相似文献   

18.
The hydrolyzed titania residue with mainly precipitated hydrated TiO2 is prepared from mechanically activated Panzhihua ilmenite leached by hydrochloric acid. We use H2O2 as a coordination agent to leach Ti from the hydrolyzed titania residue. The effects of H2O2 to-hydrolyzed titania residue mass ratio, leaching pH value, leaching temperature, leaching time, and H2O2 concentration on leaching of hydrolyzed titania residue by H2O2 are investigated. The recovery of Ti is above 98% under the optimal conditions. XRD shows that the peroxo-titania powder prepared by boiling the aqueous titanium peroxide solution is crystalline anatase phase. A well-crystallized anatase TiO2 and rutile TiO2 can be obtained through calcining at the temperature of 800 and 1000 °C, respectively. EDS shows that the impurities including silicon are enriched in the leaching slag. Little Si is detected as the only impurity in the synthetic TiO2 due to the weak alkaline condition of leaching.  相似文献   

19.
The Luojiahe Cu deposit in the Zhongtiaoshan region is located in the southern margin of the North China Craton. The orebodies are hosted in the mafic volcanic-sedimentary sequences of the metamorphosed (greenschist-facies) Neoarchean Songjiashan Group. The Luojiahe Cu mineralization can be divided into the primary volcanogenic massive sulfide (VMS) mineralization stage (Stage I, banded or stockwork ores) and the subsequent metamorphic remobilization stage (Stage II, coarse-vein ores).Three types of quartz selected for fluid inclusion (FI) studies were collected from the Stage I banded (Q1) and stockwork (Q2) ores and Stage II coarse-vein (Q3) ores. Four types of FIs were identified: (1) liquid-rich FIs (L-type), (2) pure vapor and vapor-rich FIs (V-type), (3) daughter mineral-bearing FIs (S-type), and (4) CH4-H2O FIs (C-type). Systematical microthermometric and H-O isotopic studies show that the Stage I ore-forming fluids consist predominantly of high salinity evolved seawater (125–220 °C; 23.9–27.9 wt.% NaCl equiv.) and some magmatic-hydrothermal fluids (249–339 °C; 34.5–42.2 wt.% NaCl equiv.). The two fluid end-members are represented by the L-type FIs in Q1 and the S- and V-type FIs in Q2. The temperature- and salinity variation trends of the L-type FIs in Q1 indicate a mixing process between the hot evolved seawater and cold seawater at Stage I. Furthermore, the V- and S-type FI coexistence in Q2 and their microthermometric data suggest that fluid unmixing has occurred in original magmatic fluids at Stage I. In contrast, the Stage II ore-forming fluids consist of CH4-rich metamorphic fluids (192–350 °C; 10.6–43.2 wt.% NaCl equiv.). Carbon isotopic analysis of the Stage II calcite (− 4.58 to − 10.83‰) and graphite (− 32.01 to − 39.16‰) in the ore-hosting chlorite schist indicates that the metamorphic ore-forming fluids had exchanged carbon isotope with graphite. The generation of CH4 may have resulted from the interaction between H2O (released by metamorphic devolatilization) and graphite. The continuous consumption of H2O in the hydrothermal fluid system may have increased the fluid salinity and triggered fluid unmixing in the CH4-NaCl-H2O system. In addition, the VMS metallogenic environment is generally favorable for microbial communities. It is considered that the graphite at Luojiahe may have been derived from sedimentary organic matter formed in seafloor hydrothermal vent systems, as also supported by carbon isotopic data.We propose that at Stage I, the main mineralization may have been resulted from 1) fluid mixing of hot evolved seawater and cold seawater in the near-surface environment; and 2) fluid unmixing caused by the percolation of magmatic fluids into syn-volcanic faults, forming the stockwork ores. At Stage II, the interaction between H2O and graphite may have resulted in the reduction of ore-forming fluids and Cu precipitation, and fluid unmixing in the CH4-NaCl-H2O system may have further promoted the Cu mineralization.  相似文献   

20.
《Applied Geochemistry》2006,21(9):1593-1612
Sediments, mosses and algae, collected from lake catchments of the Larsemann Hills, East Antarctica, were analysed to establish baseline levels of trace metals (Ag, As, Cd, Co, Cr, Cu, Ni, Sb, Pb, Se, V and Zn), and to quantify the extent of trace metal pollution in the area. Both impacted and non-impacted sites were included in the study. Four different leaching solutions (1 M MgCl2, 1 M CH3COONH4, 1 M NH4NO3, and 0.3 N HCl) were tested on the fine fraction (<63 μm) of the sediments to extract the mobile fraction of trace metals derived from human impact and from weathering of basement lithologies. Results of these tests indicate that dilute HCl partly dissolves primary minerals present in the sediment, thus leading to an overestimate of the mobile trace metal fraction. Concentrations of trace metals released using the other 3 procedures indicate negligible levels of anthropogenic contribution to the trace metal budget. Data derived from this study and a thorough characterisation of the site allowed the authors to define natural baseline levels of trace metals in sediments, mosses and algae, and their spatial variability across the area. The results show that, with a few notable exceptions, human activities at the research stations have contributed negligible levels (lower than natural variability) of trace metals to the Larsemann Hills ecosystem. This study further demonstrates that anthropogenic sources of trace metals can be correctly identified and quantified only if natural baselines, their variability, and processes controlling the mobility of trace metals in the ecosystem, have been fully characterised.  相似文献   

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