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1.
The orogenic gold deposits in Southeast Guizhou are an important component of the Xuefeng polymetallic ore belt and have significant exploration potential, but geochronology research on these gold deposits is scarce. Therefore, the ore genetic models are poorly constrained and remain unclear. In the present study, two important deposits(Pingqiu and Jinjing) are investigated, including combined Re-Os dating and the He-Ar isotope study of auriferous arsenopyrites. It is found that the arsenopyrites from the Pingqiu gold deposit yielded an isochron age of 400 ± 24 Ma,with an initial ~(187)Os/~(188)Os ratio of 1.24 ± 0.57(MSWD = 0.96). An identical isochron age of 400 ± 11 Ma with an initial ~(187)Os/~(188)Os ratio of 1.55 ± 0.14(MSWD = 0.34) was obtained from the Jinjing deposit. These ages correspond to the regional Caledonian orogeny and are interpreted to represent the age of the main stage ore. Both initial ~(187)Os ratios suggest that the Os was derived from crustal rocks. Combined with previous rare earth element(REE), trace elements, Nd-Sr-S-Pb isotope studies on scheelite, inclusion fluids with other residues of gangue quartz, and sulfides from other gold deposits in the region, it is suggested that the ore metals from Pingqiu and Jinjing were sourced from the Xiajiang Group. The He and Ar isotopes of arsenopyrites are characterized by ~3 He/~4 He ratios ranging from 5.3 × 10~(-4) Ra to 2.5 × 10~(-2) Ra(Ra = 1.4 × 10~(-6), the ~3 He/~4 He ratio of air), 40 Ar=/~4 He ratios from 0.64 × 10~(-2) to 15.39×10~(-2), and ~(40)Ar/~(36)Ar ratios from 633.2 to 6582.0. Those noble gas isotopic compositions of fluid inclusions also support a crustal source origin,evidenced by the Os isotope. Meanwhile, recent noble gas studies suggest that the amount of in situ radiogenic ~4 He generated should not be ignored, even when Th and U are present at levels of only a few ppm in host minerals. 相似文献
2.
甘肃阳山金矿床含砷黄铁矿及毒砂的XPS研究 总被引：9，自引：4，他引：5
阳山金矿是西秦岭地区新发现的超大型金矿.载金矿物中元素的赋存状态是认识成矿机理、评价矿床采选冶过程对环境影响的重要依据.作者运用XPS技术测定了载金矿物含砷黄铁矿和毒砂新鲜断裂面的As3d、Fe2p及S2p的存在形式和相对原子百分含量.结果表明,在含砷黄铁矿表面,超过50%的As以As~(-1)形式存在,约18%～20%的As以As~(3+)形式存在,约30%的As以As~(5+)形式存在.在毒砂表面,超过60%的As以As~(1-)形式存在,约30%的As~(3+)形式存在,其余10%的As主要以As~(3+)形式存在.分析证明As、Fe、S等元素在含砷黄铁矿和毒砂中主要以As`(1-)、Fe~(2+)、S~(1-)形式存在外,As元素可能还以As~(3+)形式存在于含砷黄铁矿及毒砂结构中. 相似文献
3.
Fe L-, S L-, and O K-edge X-ray absorption spectra of natural monoclinic and hexagonal pyrrhotites, Fe1-xS, and arsenopyrite, FeAsS, have been measured and compared with the spectra of minerals oxidized in air and treated in aqueous acidic solutions, as well as with the previous XPS studies. The Fe L-edge X-ray absorption near-edge structure (XANES) of vacuum-cleaved pyrrhotites showed the presence of, aside from high-spin Fe2+, small quantity of Fe3+, which was higher for a monoclinic mineral. The spectra of the essentially metal-depleted surfaces produced by the non-oxidative and oxidative acidic leaching of pyrrhotites exhibit substantially enhanced contributions of Fe3+ and a form of high-spin Fe2+ with the energy of the 3d orbitals increased by 0.3–0.8 eV; low-spin Fe2+ was not confidently distinguished, owing probably to its rapid oxidation. The changes in the S L-edge spectra reflect the emergence of Fe3+ and reduced density of S s–Fe 4s antibonding states. The Fe L-edge XANES of arsenopyrite shows almost unsplit eg band of singlet Fe2+ along with minor contributions attributable to high-spin Fe2+ and Fe3+. Iron retains the low-spin state in the sulphur-excessive layer formed by the oxidative leaching in 0.4 M ferric chloride and ferric sulphate acidic solutions. The S L-edge XANES of arsenopyrite leached in the ferric chloride, but not ferric sulphate, solution has considerably decreased pre-edge maxima, indicating the lesser admixture of S s states to Fe 3d orbitals in the reacted surface layer. The ferric nitrate treatment produces Fe3+ species and sulphur in oxidation state between +2 and +4. 相似文献
4.
Soil, mine tailing, and waste dump profiles above three mesothermal gold deposits in the Bohemian Massif with different anthropogenic histories have been studied. Their mineralogical, major element, and arsenic (As) contents and the contents of secondary arsenic minerals were analyzed. The As-bearing minerals were concentrated and determined using X-ray diffraction (XRD) analysis, the Debye-Scherrer powder method, scanning electron microscopy (SEM), and energy-dispersive microanalysis (EDAX). The amorphous hydrous ferric oxides (HFO), As-bearing goethite, K-Ba- or Ca-Fe- and Fe- arsenates pharmacosiderite, arseniosiderite, and scorodite, and sulfate-arsenate pitticite were determined as products of arsenopyrite or arsenian pyrite oxidation. The As behaviour in the profiles studied differs in dependence on the surface morphology, chemical and mineralogical composition of the soil, mine wastes or tailings, oxidation conditions, pH, presence of (or distance from) primary As mineralization in the bedrock, and duration of the weathering effect. Although the primary As mineralization and the bedrock chemical composition are roughly similar, there are distinct differences in the As behaviour amongst the Mokrsko, Roudný and Kaperské Hory deposits. 相似文献
5.
A. López Valdivieso A.A. Sánchez López C. Ojeda Escamilla M.C. Fuerstenau 《International Journal of Mineral Processing》2006
The role of pH and pulp redox potential (EH) to control the flotation and depression of arsenopyrite has been investigated through studies on microflotation of arsenopyrite crystals and batch flotation of an arsenopyritic ore using isopropyl xanthate as collector. The transition between flotation and depression of arsenopyrite is established by the reversible potential of the xanthate/dixanthogen couple. Adsorption of arsenate ions on ferric hydroxide has been studied through electrokinetics to delineate mechanisms involved in the depression of arsenopyrite using oxidants. Chemical binding between arsenate species and ferric hydroxide sites on arsenopyrite is suggested as the mechanism responsible for depression of arsenopyrite. EH conditions are given for the flotation and depression of arsenopyite at various pH values for the arsenopyritic ore. 相似文献
6.
大平山铜矿床位于南京市江宁区横溪镇西侧,矿石中有用组分除铜以外,还伴生有As、Zn、Ag、Au、Co和Ni等元素,其中As元素质量分数较高,局部达0.2%～0.9%。通过显微观察和扫描电镜能谱分析,发现大平山铜矿矿石中As元素主要以硫化物形式,呈毒砂独立矿物以自形—半自形粒状、他形粒状赋存于矿石中。赋存方式主要为：以独立矿物呈稀疏浸染状分布于矿石中,局部呈条带状和中等稠密浸染状分布于矿石中;以交代方式与黄铁矿和黄铜矿共生于矿石中,但毒砂形成晚于黄铁矿和黄铜矿。 相似文献
7.
The gold–tourmaline quartz–vein deposit of Passagem de Mariana, in the southeastern part of the Quadrilátero Ferrífero, produced more than 60 tonne of gold, from the end of the 17th Century until 1954. The mine has not operated since 1985. Orebodies are veins composed of white quartz (> 60 vol.%), carbonate (ankerite), tourmaline, sericite and sulfides. Tourmaline (dravite), up to 10 vol.% of the vein, occurs as subhedral, coarse, commonly zoned crystals, and is concentrated along vein boundaries and on the edges of host rock inclusions in the veins. Tourmaline is present in all rock types in the mine, but the chemical composition of the host rocks determinates the intensity of tourmalinization, with the alteration being greater in sericitic phyllites, graphite–sericite phyllites, and calcareous rocks. The most abundant sulfide is arsenopyrite, which is normally associated with pyrite and pyrrhotite. Minor amounts of chalcopyrite, galena, löllingite, berthierite, and maldonite are present throughout the deposit. Sulfides are concentrated at veins boundary or are dispersed in the veins. Arsenopyrite is associated, most commonly, with calcareous rocks, and graphite–sericite phyllite. Pyrrhotite is usually found at the base of itabirites. Gold abundance is directly proportional to sulfide concentration. Hydrothermal alteration associated with the veins includes silicification, tourmalinization, and sulfidation. The mineralized zone is a shear zone associated with a bedding-parallel thrust fault that juxtaposes the itabirite (Lower Proterozoic Minas Supergroup) over other units. This shear zone/thrust fault extends for tens of km beyond the Passagem mine and hosts numerous gold deposits. The richest orebodies are along the itabirite footwall contact and within the graphite–sericite phyllite (Main orebody). Although many lithologic units were mineralized the graphite–sericite phyllite appears to have been most favorable for gold deposition.The area underwent three phases of deformation, D1, D2 and D3. Mineral assemblages indicate upper-greenschist to lower-amphibolite conditions of regional metamorphism. Retrograde metamorphism, characterized by chloritization of biotite and chloritization and biotitization of garnet, developed locally. The gold-bearing veins crosscut the main foliation and lithologic contacts at low angle and occur within, or are in contact with, all lithotypes. Field and laboratory data indicate that gold mineralization at Passagem de Mariana is epigenetic. Gold deposition occurred after the peak of metamorphism, within the late- to post-D2 period of deformation, which is correlated with second set of structures of Trasamazonian age of Alkmim and Marshak [Alkmim, F.F., Marshak, S., 1998. Transamazonian Orogeny in the Southern São Francisco Craton Region, Minas Gerais, Brazil: evidence for Paleoproterozoic collision and collapse in the Quadrilátero Ferrífero. Precambrian Research 90, 29-58.], indicating that the gold mineralization occurred between 2.124 and 2.04 Ga. We choose to regard Passagem de Marina as an orogenic gold deposit as defined by Groves et al. [Groves, D. I., Goldfarb, R.J., Gebre-Mariam, M., Hagemann, S.G., Robert, F., 1998. Orogenic gold deposits: A proposed classification in the context of their crustal distribution and relationship to other gold deposit types. Ore Geology Reviews 13, 7-27.], i.e., an epigenetic, structurally-hosted lode–gold vein system in a deformed metamorphic terrane. 相似文献
8.
A minesoil has developed over 5 years oxidative exposure on sulphide concentrate tailings (ca. 1 wt.% As) at the Macraes mesothermal gold mine, New Zealand. The minesoil has a dry crust which has formed due to evaporative drying. This dry crust is enriched in arsenic (ca. 5 wt.% As) as scorodite (FeAsO4·2H2O) because of upward mobility of dissolved arsenic during drying. Similar enrichment of arsenic has occurred along the walls of desiccation cracks which extend over 1 m into the minesoil. Capping of the tailings and minesoil with wet tailings (pH=8) results in dissolution of scorodite and remobilization of arsenic on the millimetre scale. Experimental capping of the minesoil with wet calcium carbonate remobilized some arsenic from scorodite on the centimetre scale, but much original arsenic enrichment was preserved after 400 days. A layer of gypsum (CaSO4·2H2O) and iron oxyhydroxide cementation developed at the interface between the minesoil and the experimental calcium carbonate cap, restricting water flow. This layer was ca. 1 mm thick after 400 days. Theoretical comparison between advection and diffusion in the minesoil suggests that diffusion is an important mechanism for chemical mobility on the 1–50-year time scale. However, advection can be important in secondary porosity of the dry crust of the minesoil and water penetrates this zone at a rate of 1.5 mm/day. 相似文献
9.
哈图金矿蚀变岩型矿体特征及金赋存状态研究 总被引：1，自引：0，他引：1
哈图金矿由石英脉型和蚀变岩型矿体组成,蚀变岩型矿体遭受了强烈黄铁矿化、毒砂化、碳酸盐化、硅化和绢云母化蚀变.成矿作用划分5个阶段:钠长石-石英阶段(I)、黄铁矿-碳酸盐-石英阶段(II)、黝铜矿-黄铜矿-自然金阶段(III)、毒砂-碳酸盐-绢云母阶段(IV)和方解石-石英阶段(V).其中,II—IV阶段是主要金成矿阶段.哈图金矿含金矿物主要为自然金,平均成色912.自然金呈裂隙金、包裹金、粒间金形式嵌布在黄铁矿和毒砂中.当载金矿物为黄铁矿时,自然金与黝铜矿-黄铜矿-闪锌矿关系密切;当载金矿物为毒砂时,自然金与黄铁矿-黄铜矿关系密切. 相似文献
10.
金及多金属矿化破碎蚀变带与逆断层关系密切,柱状、针状白色毒砂及细微粒黄铁矿是金的重要标志性矿物,成矿带具有良好的成矿地球化学背景和成矿地质条件,良好的控矿、容矿构造条件。 相似文献