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1.
A diagnostic leaching showed that partial oxidation of the sulphide minerals in a gold ore was beneficial for thiosulphate leaching of gold. A pre-treatment process with oxidative ammoniacal solution enhanced the thiosulphate leaching of the sulphide ore, while the thiosulphate consumption was substantially reduced. The sulphide minerals partially decomposed in the pre-treatment process, exposing gold to the leach solution. Oxygen input by air bubbling and a longer contact time enhanced the oxidative ammonia pre-treatment process and hence accelerated subsequent thiosulphate leaching of the sulphide ore. Gold extraction in 0.8 M ammonia and 0.1 M thiosulphate solution after 24 h increased from 69% without pre-treatment to 81%, 84%, 90% and 94% respectively after 1, 3, 7 and 22 h pre-treatment. The consumption of sodium thiosulphate was 2.37 kg/t after 24 h leaching without pre-treatment, but was negligible after over 1 h oxidative ammonia pre-treatment. A counter-current leaching process was conducted in the leaching of the sulphide ore. The fresh leachant still gave higher leaching rates in contact with the pre-leached ore, while the pre-used leachant had significantly lower leaching kinetics and overall gold extraction in contact with the fresh ore. This 2-step counter-current leaching process proved that the leachant, other than the passivation, was the determinant factor causing the gold leaching rates to decrease after a certain time of leaching. The findings enable the thiosulphate leaching of high sulphide containing gold ores to be more efficient at lower thiosulphate consumption following the oxidative ammoniacal pre-treatment.  相似文献   

2.
张永奎  宋航 《矿物岩石》2003,23(4):80-84
四川某金矿是一种难浸金矿，因为矿石中的金被包裹于含铁硫化矿物中，而且含有机炭质物。细菌Hst能有效氧化金矿中的硫化矿物以提高金的浸出率。如果细菌氧化矿石中铁的浸出率大于90％，金几乎完全解离，金的氰化浸出率大于90％。研究表明，该金矿的难浸特性是因为金包裹于含铁硫化矿物中，有机炭质物和粘土矿物对金浸出影响甚微。  相似文献   

3.
The ironstone succession at El Gedida-Ghorabi-Naser area of El Bahariya depression is subdivided into lagoonal manganiferous mud and fossiliferous ironstone consisting mainly of hematite and goethite-hydrogoethite. The application of the ASD field spectroradiometer measurements (spectral range) in the ASTER data led to the interpretation of the presence of ferruginous units as quartzitic sandstone, gluconitic sandy clay, and pink marly limestone. The existing iron ore minerals in the iron ore localities were also classified into high Mn hematite, low Mn hematite, goethite, hydrogoethite as well as low- and high-grade Hematite and Barite. Quartz, feldspars, rutile, and clay minerals (e.g., kaolinite and illite) are mainly associated with the iron ore. Accessory minerals of manganese, e.g., psilomelane and pyrolusite, were also present. The Barite mineral is recorded as a common mineral association with the iron ore deposits at El Gedida and Ghorabi localities. The stratigraphical units investigated in the study area include the oldest gravely clayey sandstones of the Bahariya Formation overlain by the fossiliferous and oolitic limestones of the El-Hamra, Qazzun, and Naqb Formations. Quartztic sandstones and clayey sandstones of the Radwan Formation and youngest Quaternary sediments of sandy-clayey materials were often found as intermittent cover and overburden in unconformity surfaces over the iron ore bands.  相似文献   

4.
Gold nuggets (centimetre scale) have formed in a supergene alteration zone on hydrothermal gold deposits, and occur intergrown with quartz and iron oxyhydroxide pseudomorphs after sulphide minerals, and along fractures in quartz and host rocks. The supergene alteration was driven by groundwater-driven water-rock interaction near to a regional unconformity beneath fluvial sediments, and involved clay alteration and oxidation that extended up to 50 m below the unconformity. Oxidation of pyrite and arsenopyrite produced temporary thiosulphate ligands that mobilised microparticulate gold encapsulated in the sulphide minerals. The nuggets have some crystalline form, and internally they consist of anhedral grains, elongated gold plates, and intimate intergrowths of gold and iron oxyhydroxide. Nugget surfaces have further micron scale overgrowths of microparticulate gold, gold plates, and gold crystals. Nuggets were eroded and recycled into nearby proximal Miocene quartz pebble conglomerates, where they concentrated in placers near the basal unconformity. Later recycling transferred gold into Pleistocene fluvial channels. Gold dissolution and redeposition as plates and crystals occurred on the exterior surfaces of placer gold particles, with little change in mass. All groundwater maintained high pH throughout the geological history because there was sufficient calcite in the basement rocks to neutralise any acid generated by pyrite oxidation. Hence, gold mobility in sediments was driven by thiosulphate complexes as for the in situ nuggets, albeit with lower dissolved sulphur concentrations. Despite aridification of the climate in the late Cenozoic, with resulting localised high dissolved chloride concentrations, chloride complexation did not contribute to gold mobility.  相似文献   

5.
蔡淑霞  张云 《地质与资源》1992,1(4):235-242
本文介绍了堆浸提金原理和在实验室进行金矿石堆浸可行性研究的方法.以我国辽宁猫岭金矿、四川茶铺子金矿和福建紫金山金矿为研究对象,研究了矿石粒度、氰化钠溶液浓度、浸出时间等因素对金浸出率的影响,从而确定堆浸提金最佳工艺条件.通过对上述三类矿石性质及堆浸性能的比较,认为矿石的物质组成和金的嵌布特性对金的浸出率影响较大.  相似文献   

6.
马俊  赵占清 《吉林地质》1999,18(2):46-49
本文从赤卫沟金矿的矿石性质、矿石加工、池浸方法、金银回收方面,介绍了贫硫化物、金颗粒细微、有一定氧化程度的金矿池浸生产实践。从而推荐一种简便、回收率高、投资少、见效快的提工方法－池浸,以便促进矿业开发工作更快发展。  相似文献   

7.
The Hadamengou gold deposit is located in western part of the northern margin of the North China craton. It is a hydrothermal deposit related to alkaline magmatism. Dissolution of Au, Fe from pyrite and iron oxide （including magnetite and hematite） individual minerals in the three main types of ore shows： in iron oxides （magnetite and hematite）, Au and Fe were dissolved simultaneously and their solubilities are positively correlated, which means Au is mainly chemical-bonded （lattice gold） and/or colloidal-adsorbed in iron oxides; while in pyrite, on the contrary, Au dissolution obviously lags behind Fe and the solubility of Au shows negative relationship with that of Fe, which indicates Au is mainly hosted as grains of elemental gold （or native gold） within pyrite. Previous studies revealed that the Hadamengou gold deposit is characterized by intensive K-feldspathization and holds high content of iron oxides occasionally replaced by sulfides, which was caused by oxidizing K-enriched alkaline fluids under a stretching geodynamic setting. These geological features, together with the high Au-content in iron oxides, comparable with that of the Olympic Dam deposit in South Australia, suggest that this deposit is the first example of iron oxide-type gold deposits in China.  相似文献   

8.
国内外铁矿石价格对标基准多采用离岸价或到岸价,而非盈亏平衡运营成本,难以揭示我国铁矿石所面对的真实市场承压价格。为了厘清国际一线生产商的铁矿石盈亏平衡运营成本价格,本文对世界上最重要的条带状铁建造（BIF）矿产地——西澳哈默斯利盆地高品位赤铁矿矿床的矿化特征及代表性铁矿石产品展开系统研究,同时引入巴西铁四角地区的铁英岩型赤铁矿矿石作为对照,分析全球典型高品位赤铁矿矿石经济指标。结合前人研究成果,将西澳哈默斯利盆地与BIF相关的高品位赤铁矿的富集矿化类型划分为假象赤铁矿-针铁矿、微板状赤铁矿与河道沉积型赤铁矿,巴西铁四角主要为铁英岩型赤铁矿。上述各矿化类型对应的铁矿石产品的铁元素含量均高于56%;在杂质元素含量上,假象赤铁矿-针铁矿的磷含量高,微板状赤铁矿的磷、硫含量较高,河道沉积型赤铁矿的磷、硫含量较低,铁英岩型赤铁矿含锰。经定量估算,西澳力拓、必和必拓、FMG和巴西淡水河谷的铁矿石盈亏平衡运营成本价格分别为34.66、36.76、47.35、38.07美元/干吨,可为中国海外权益铁矿项目开发提供运营成本的参考。  相似文献   

9.
The effect of carbon or graphite coating on the adsorption of gold cyanide on pyrite was investigated with pure pyrite and a pyrite concentrate. In the carbon or graphite-contaminated pyrite systems carbon and graphite not only acted as gold sorbents, but also enhanced gold adsorption on pyrite. The carbon coating enhanced gold adsorption on pyrite to a larger extent, in comparison with the graphite coating. The carbon or graphite coating on pyrite reduced the negativity of the pyrite surfaces, and hence improved the physical adsorption of gold cyanide on pyrite. In addition, the highly conductive coating of carbon or graphite on pyrite could enhance electron transfer in the electrochemical reactions occurring in the chemical adsorption of gold and gold reduction on pyrite. The preg-robbing by pyrite or the graphite-coated pyrite was reduced and further eliminated at higher cyanide concentrations. However, gold adsorption on the carbon-coated pyrite could not be prevented even at higher cyanide concentrations due to gold adsorption on the carbon coating. In comparison with pure pyrite, the pyrite concentrate had a higher capacity adsorbing gold, due to the presence of carbonaceous matter in the pyrite concentrate. Fine grinding intensified the smearing of carbon or graphite on the mineral particles, resulting in a larger extent of enhancement in the preg-robbing of the concentrate by the carbon or graphite coating.A diagnostic elution of the preg-robbing pyrite samples indicated that the reduction of gold at the pyrite surfaces was the dominant mechanism for gold adsorption on pyrite, followed by physical and chemical adsorption. Surface topological studies by SEM/EDX showed that gold adsorbed at defect sites on pyrite surfaces. For the pyrite with a 5% carbon coating, gold was observed to adsorb not only at the defect sites, but also at the smooth surfaces with carbon present. For the pyrite with a 5% graphite coating, carbon was also found at the pyrite surfaces, but gold was only detected at the defect sites. XPS studies revealed that part of the gold physically and chemically adsorbed on pyrite or pyrite coated with carbon or graphite. Some gold cyanide was reduced at the pyrite surfaces, with the sulphide ions of pyrite being oxidised to elemental sulphur.  相似文献   

10.
The effect of carbon or graphite coating on the adsorption of gold cyanide on pyrite was investigated with pure pyrite and a pyrite concentrate. In the carbon or graphite contaminated pyrite systems carbon and graphite not only acted as gold sorbents, but also enhanced gold adsorption on pyrite. The carbon coating enhanced gold adsorption on pyrite to a larger extent, in comparison with the graphite coating. The carbon or graphite coating on pyrite reduced the negativity of the pyrite surfaces, and hence improved the physical adsorption of gold cyanide on pyrite. In addition, the highly conductive coating of carbon or graphite on pyrite could enhance electron transfer in the electrochemical reactions occurring in the chemical adsorption of gold and gold reduction on pyrite. The preg-robbing by pyrite or the graphite-coated pyrite was reduced and further eliminated at higher cyanide concentrations. However, gold adsorption on the carbon-coated pyrite could not be prevented even at higher cyanide concentrations due to gold adsorption on the carbon coating. In comparison with pure pyrite, the pyrite concentrate had a higher capacity adsorbing gold, due to the presence of carbonaceous matter in the pyrite concentrate. Fine grinding intensified the smearing of carbon or graphite on the mineral particles, resulting in a larger extent of enhancement in the preg-robbing of the concentrate by the carbon or graphite coating.A diagnostic elution of the preg-robbing pyrite samples indicated that the reduction of gold at the pyrite surfaces was the dominant mechanism for gold adsorption on pyrite, followed by physical and chemical adsorption. Surface topological studies by SEM/EDX showed that gold adsorbed at defect sites on pyrite surfaces. For the pyrite with a 5% carbon coating, gold was observed to adsorb not only at the defect sites, but also at the smooth surfaces with carbon present. For the pyrite with a 5% graphite coating, carbon was also found at the pyrite surfaces, but gold was only detected at the defect sites. XPS studies revealed that part of the gold physically and chemically adsorbed on pyrite or pyrite coated with carbon or graphite. Some gold cyanide was reduced at the pyrite surfaces, with the sulphide ions of pyrite being oxidised to elemental sulphur.  相似文献   

11.
The BIF-hosted iron ore system represents the world's largest and highest grade iron ore districts and deposits. BIF, the precursor to low- and high-grade BIF hosted iron ore, consists of Archean and Paleoproterozoic Algoma-type BIF (e.g., Serra Norte iron ore district in the Carajás Mineral Province), Proterozoic Lake Superior-type BIF (e.g., deposits in the Hamersley Province and craton), and Neoproterozoic Rapitan-type BIF (e.g., the Urucum iron ore district).The BIF-hosted iron ore system is structurally controlled, mostly via km-scale normal and strike-slips fault systems, which allow large volumes of ascending and descending hydrothermal fluids to circulate during Archean or Proterozoic deformation or early extensional events. Structures are also (passively) accessed via downward flowing supergene fluids during Cenozoic times.At the depositional site the transformation of BIF to low- and high-grade iron ore is controlled by: (1) structural permeability, (2) hypogene alteration caused by ascending deep fluids (largely magmatic or basinal brines), and descending ancient meteoric water, and (3) supergene enrichment via weathering processes. Hematite- and magnetite-based iron ores include a combination of microplaty hematite–martite, microplaty hematite with little or no goethite, martite–goethite, granoblastic hematite, specular hematite and magnetite, magnetite–martite, magnetite-specular hematite and magnetite–amphibole, respectively. Goethite ores with variable amounts of hematite and magnetite are mainly encountered in the weathering zone.In most large deposits, three major hypogene and one supergene ore stages are observed: (1) silica leaching and formation of magnetite and locally carbonate, (2) oxidation of magnetite to hematite (martitisation), further dissolution of quartz and formation of carbonate, (3) further martitisation, replacement of Fe silicates by hematite, new microplaty hematite and specular hematite formation and dissolution of carbonates, and (4) replacement of magnetite and any remaining carbonate by goethite and magnetite and formation of fibrous quartz and clay minerals.Hypogene alteration of BIF and surrounding country rocks is characterised by: (1) changes in the oxide mineralogy and textures, (2) development of distinct vertical and lateral distal, intermediate and proximal alteration zones defined by distinct oxide–silicate–carbonate assemblages, and (3) mass negative reactions such as de-silicification and de-carbonatisation, which significantly increase the porosity of high-grade iron ore, or lead to volume reduction by textural collapse or layer-compaction. Supergene alteration, up to depths of 200 m, is characterised by leaching of hypogene silica and carbonates, and dissolution precipitation of the iron oxyhydroxides.Carbonates in ore stages 2 and 3 are sourced from external fluids with respect to BIF. In the case of basin-related deposits, carbon is interpreted to be derived from deposits underlying carbonate sequences, whereas in the case of greenstone belt deposits carbonate is interpreted to be of magmatic origin. There is only limited mass balance analyses conducted, but those provide evidence for variable mobilization of Fe and depletion of SiO2. In the high-grade ore zone a volume reduction of up to 25% is observed.Mass balance calculations for proximal alteration zones in mafic wall rocks relative to least altered examples at Beebyn display enrichment in LOI, F, MgO, Ni, Fe2O3total, C, Zn, Cr and P2O5 and depletions of CaO, S, K2O, Rb, Ba, Sr and Na2O. The Y/Ho and Sm/Yb ratios of mineralised BIF at Windarling and Koolyanobbing reflect distinct carbonate generations derived from substantial fluid–rock reactions between hydrothermal fluids and igneous country rocks, and a chemical carbonate-inheritance preserved in supergene goethite.Hypogene and supergene fluids are paramount for the formation of high-grade BIF-hosted iron ore because of the enormous amount of: (1) warm (100–200 °C) silica-undersaturated alkaline fluids necessary to dissolve quartz in BIF, (2) oxidized fluids that cause the oxidation of magnetite to hematite, (3) weakly acid (with moderate CO2 content) to alkaline fluids that are necessary to form widespread metasomatic carbonate, (4) carbonate-undersaturated fluids that dissolve the diagenetic and metasomatic carbonates, and (5) oxidized fluids to form hematite species in the hypogene- and supergene-enriched zone and hydroxides in the supergene zone.Four discrete end-member models for Archean and Proterozoic hypogene and supergene-only BIF hosted iron ore are proposed: (1) granite–greenstone belt hosted, strike-slip fault zone controlled Carajás-type model, sourced by early magmatic (± metamorphic) fluids and ancient “warm” meteoric water; (2) sedimentary basin, normal fault zone controlled Hamersley-type model, sourced by early basinal (± evaporitic) brines and ancient “warm” meteoric water. A variation of the latter is the metamorphosed basin model, where BIF (ore) is significantly metamorphosed and deformed during distinct orogenic events (e.g., deposits in the Quadrilátero Ferrífero and Simandou Range). It is during the orogenic event that the upgrade of BIF to medium- and high-grade hypogene iron took place; (3) sedimentary basin hosted, early graben structure controlled Urucum-type model, where glaciomarine BIF and subsequent diagenesis to very low-grade metamorphism is responsible for variable gangue leaching and hematite mineralisation. All of these hypogene iron ore models do not preclude a stage of supergene modification, including iron hydroxide mineralisation, phosphorous, and additional gangue leaching during substantial weathering in ancient or Recent times; and (4) supergene enriched BIF Capanema-type model, which comprises goethitic iron ore deposits with no evidence for deep hypogene roots. A variation of this model is ancient supergene iron ores of the Sishen-type, where blocks of BIF slumped into underlying karstic carbonate units and subsequently experienced Fe upgrade during deep lateritic weathering.  相似文献   

12.
The intensification of the thiosulphate leaching of silver from a silver-bearing complex sulphide concentrate (Casapalca deposit) using mechanochemical alkaline leaching as the pretreatment step was investigated. The leaching of “as-received” concentrate with the thiosulphate solution afforded only 6% recovery of Ag into leach. The mechanochemical pretreatment resulted 85% amorphization of tetrahedrite as a silver-bearing mineral in the concentrate as well as an increase in specific surface area from the original value of 0.26 m2 g−1 to a maximum value of 15.7 m2 g−1. The pretreatment was performed in a stirred ball mill using variable milling times and sample weights. The physico-chemical changes in the concentrate as a consequence of mechanochemical pretreatment had a pronounced influence on the subsequent silver extraction. The optimum results from mechanochemical pretreatment and subsequent leaching of the concentrate with ammonium thiosulphate were achieved by using a milling time of 60 min and a weight of sample of 60 g. In this case, 99% recovery of Ag was achieved after only 3 min of leaching.  相似文献   

13.
An oxide gold ore was subjected to chloride/hypochlorite leaching at room temperature. The effects of three factors, including Ca(OCl)2 vs. NaOCl, OCl− concentration, and HCl concentration on gold leaching performance were investigated. Due to formation of CaOCl+ complex in solution and hence less reactivity, calcium hypochlorite produces a sluggish gold leaching kinetics, taking twice the time (46 h) to achieve maximum gold recovery of 58% compared to sodium hypochlorite. 10 g/L of total initial hypochlorite species in solution produces reasonable gold recoveries. The amount of added HCl and hence the initial pH was found to have a major effect on gold leaching kinetics and maximum gold recovery. A high level of 9 g/L of added HCl causes HClO to be very reactive, producing very fast kinetics, reaching 67% gold extraction in 4 h. It also causes a faster consumption of hypochlorous acid, through catalytic decomposition (by NiO and CuO) and disproportionation. Hypochlorous acid reactions with sulfide and ferrous content of ore proceed very slowly in the pH range of 4–11. Gold–chloro complexes are strongly adsorbed on quartz component of ore. To minimize this undesirable adsorption of gold–chloro species, the aging time must be limited to a few hours only.  相似文献   

14.
The Blue Dot gold deposit, located in the Archean Amalia greenstone belt of South Africa, is hosted in an oxide (± carbonate) facies banded iron formation (BIF). It consists of three stratabound orebodies; Goudplaats, Abelskop, and Bothmasrust. The orebodies are flanked by quartz‐chlorite‐ferroan dolomite‐albite schist in the hanging wall and mafic (volcanic) schists in the footwall. Alteration minerals associated with the main hydrothermal stage in the BIF are dominated by quartz, ankerite‐dolomite series, siderite, chlorite, muscovite, sericite, hematite, pyrite, and minor amounts of chalcopyrite and arsenopyrite. This study investigates the characteristics of gold mineralization in the Amalia BIF based on ore textures, mineral‐chemical data and sulfur isotope analysis. Gold mineralization of the Blue Dot deposit is associated with quartz‐carbonate veins that crosscut the BIF layering. In contrast to previous works, petrographic evidence suggests that the gold mineralization is not solely attributed to replacement reactions between ore fluid and the magnetite or hematite in the host BIF because coarse hydrothermal pyrite grains do not show mutual replacement textures of the oxide minerals. Rather, the parallel‐bedded and generally chert‐hosted pyrites are in sharp contact with re‐crystallized euhedral to subhedral magnetite ± hematite grains, and the nature of their coexistence suggests that pyrite (and gold) precipitation was contemporaneous with magnetite–hematite re‐crystallization. The Fe/(Fe+Mg) ratio of the dolomite–ankerite series and chlorite decreased from veins through mineralized BIF and non‐mineralized BIF, in contrast to most Archean BIF‐hosted gold deposits. This is interpreted to be due to the effect of a high sulfur activity and increase in fO2 in a H2S‐dominant fluid during progressive fluid‐rock interaction. High sulfur activity of the hydrothermal fluid fixed pyrite in the BIF by consuming Fe2+ released into the chert layers and leaving the co‐precipitating carbonates and chlorites with less available ferrous iron content. Alternatively, the occurrence of hematite in the alteration assemblage of the host BIF caused a structural limitation in the assignment of Fe3+ in chlorite which favored the incorporation of magnesium (rather than ferric iron) in chlorite under increasing fO2 conditions, and is consistent with deposits hosted in hematite‐bearing rocks. The combined effects of reduction in sulfur contents due to sulfide precipitation and increasing fO2 during progressive fluid‐rock interactions are likely to be the principal factors to have caused gold deposition. Arsenopyrite–pyrite geothermometry indicated a temperature range of 300–350°C for the associated gold mineralization. The estimated δ34SΣS (= +1.8 to +2.5‰) and low base metal contents of the sulfide ore mineralogy are consistent with sulfides that have been sourced from magma or derived by the dissolution of magmatic sulfides from volcanic rocks during fluid migration.  相似文献   

15.
YML铁矿区位于几内亚福雷卡里亚省,富铁矿以条带状赤铁矿和铁角砾岩矿为主。矿区内共发育7条矿体,条带状赤铁矿体6条,铁角砾岩矿体1条。条带状赤铁矿体赋存部位多为向形地段,次级紧密褶皱发育,沿走向和倾向有逐渐变薄和尖灭的趋势;铁角砾岩矿体覆盖于地表,以风化壳的形式出现。矿床类型属复合类型,即海底热液喷气沉积叠加后期构造变质型+风化淋滤型。该区具备铁矿形成和保存的地质条件,且已发现具一定储量、品位较高的条带状赤铁矿和大面积的铁角砾岩分布区,区内铁矿找矿远景较好。  相似文献   

16.
Heavy metal contents have been investigated in sediment and water samples from gold and platinum mining areas of South Africa. Waste waters from Witwatersrand and Orange Free State gold mines exhibit characteristically low pH-values due to the formation of sulphuric acid by oxidation of sulphide ore minerals. Acid leaching of iron, manganese, nickel, cobalt, copper and zinc effects a 1,000–10,000-fold increase of metal concentrations as compared to the respective values in unpolluted river water. Lack of carbonate buffering prevents rapid immobilization and may lead to widespread distribution of toxic metals in the aquatic systems. These findings illustrate that modern ore refining techniques have little effect on the water quality as long as unchecked hydrometallurgical processes take place outside the production plant.  相似文献   

17.
我国原矿、精矿消费量和尾矿产出量巨大,这些矿产品中有毒有害污染物的溶解释放(称为"溶出")已经成为一个普遍存在的环境问题。本文阐述了目前国内外矿产品污染物溶出的研究现状,总结了研究矿产品中污染物溶出最常用的四种模拟试验方法(湿度室试验、淋滤柱试验、静态浸泡试验、萃取试验)的应用进展。湿度室试验可模拟自然风化过程,确定污染物溶出速率和产物;淋滤柱试验可模拟降水和喷淋过程,提供污染物吸附和解吸附动力学依据;静态浸泡试验可模拟被水浸泡过程,探明溶出规律和产物;萃取试验可对污染物进行形态分析,评估介质中污染物的流动性、稳定性等。污染物溶出的各种影响因素由强到弱依次是pH值、淋溶浸泡时间、温度、固液比、矿石粒径,多数情况下pH值越大、浸泡时间越长、温度越高、固液比越小、粒径越小越有利于污染物的溶出。溶出是一个长期和具有潜伏性的过程,其内部发生一系列物理化学反应,显示出与扩散效应不同的规律。目前这方面的研究对象还主要集中于废弃的尾矿,对经运输、堆放并在人类生活区使用的原矿、精矿产品的污染物溶出有待进一步研究,需要对其溶出污染进行预测和评估,采取有效措施控制和治理矿产品的污染。  相似文献   

18.
The atomic and electronic structure of mineral surfaces affects many environmentally important processes such as adsorption phenomena. They are however rarely considered relevant to dissimilatory bacterial reduction of iron and manganese minerals. In this regard, surface area and thermodynamics are more commonly considered. Here we take a first step towards understanding the nature of the influence of mineral surface structure upon the rate of electron transfer from Shewanella oneidensis strain MR-1 outer membrane proteins to the mineral surface and the subsequent effect upon cell “activity.” Cell accumulation has been used as a proxy for cell activity at three iron oxide single crystal faces; hematite (001), magnetite (111) and magnetite (100). Clear differences in cell accumulation at, and release from the surfaces are observed, with significantly more cells accumulating at hematite (001) compared to either magnetite face whilst relatively more cells are released into the overlying aqueous phase from the two magnetite faces than hematite. Modeling of the electron transfer process to the different mineral surfaces from a decaheme (protoporphyrin rings containing a central hexacoordinate iron atom), outer membrane-bound cytochrome of S. oneidensis has been accomplished by employing both Marcus and ab initio density functional theories. The resultant model of electron transfer to the three oxide faces predicts that over the entire range of expected electron transfer distances the highest electron transfer rates occur at the hematite (001) surface, mirroring the observed cell accumulation data. Electron transfer rates to either of the two magnetite surfaces are slower, with magnetite (111) slower than hematite (001) by approximately two orders of magnitude. A lack of knowledge regarding the structural details of the heme-mineral interface, especially in regards to atomic distances and relative orientations of hemes and surface iron atoms and the conformation of the protein envelope, precludes a more thorough analysis. However, the results of the modeling concur with the empirical observation that mineral surface structure has a clear influence on mineral surface-associated cell activity. Thus surface structure effects must be accounted for in future studies of cell-mineral interactions.  相似文献   

19.
哈达门沟金矿床产于华北克拉通北缘西段，形成于伸展构造背景中，成矿流体富钾高碱且氧化性强，矿石建造中铁氧化物含量高，并且可见铁氧化物被硫化物交代的现象。文章拟揭示金在铁氧化物中的含量和赋存状态，并探讨金矿床成因。对哈达门沟金矿3种类型矿石中的黄铁矿、铁氧化物(磁铁矿和赤铁矿)单矿物进行金、铁浸取实验，结果表明：铁氧化物含金较高；黄铁矿中的金和铁的浸出曲线不同步，金浸出率与铁浸出率呈负相关，表明黄铁矿中的金主要以颗粒金形式存在；铁氧化物中金、铁同步浸出，浸出率为正相关，表明铁氧化物中的金主要以品格金和(或)胶体吸附金形式存在。哈达门沟金矿床的上述特征均表明其具铁氧化物型金矿床的特点。  相似文献   

20.
Iron and aluminium oxides are available in many climatic regions and play a vital role in many environmental processes, including the interactions of microorganisms in contaminated soils and groundwater with their ambient environment. Indigenous microorganisms in contaminated environments often have the ability to degrade or transform those contaminants, a concept that supports an in situ remediation approach and uses natural microbial populations in order to bio-remediate polluted sites. These metal oxides have a relatively high pH-dependent surface charge, which makes them good candidates for studying mineral–bacterial adhesion. Given the importance of understanding the reactions that occur at metal oxide and bacterial cell interfaces and to investigate this phenomenon further under well-characterized conditions, some of the most common iron and aluminium oxides; hematite, goethite and aluminium hydroxide, were synthesized and characterized and a coating method was developed to coat polystyrene well-plates as a surface exposable to bacterial adhesion with these minerals (non-treated polystyrene-12 well-plates which are used for cell cultures). The coating process was designed in a way that resembles naturally coated surfaces in aquifers. Hematite, Fe2O3, was synthesized from acidic FeCl3 solution, while goethite, FeOOH, and aluminium hydroxide, Al(OH)3, were prepared from an alkaline solution of Fe(NO3)3 and Al(NO3)3. They were further characterized using X-ray diffraction (XRD), Fourier transform infrared (FTIR), potentiometric titration and contact angle measurements. Characterization results show that the pure phases of hematite, goethite and aluminium hydroxides are formed with a point of zero charge (PZC) of 7.5, 8.5 and 8.9, respectively. The coating process was based on the direct deposition of mineral particles from an aqueous suspension by evaporation. Then, altered polystyrene surface properties were analyzed using X-ray photoelectron spectroscopy (XPS), attenuated total reflection-Fourier transform infrared (ATR-IR), water drop contact angle measurements and vertical scanning interferometry (VSI). The surface analysis tests prove that the coated polystyrene surface has physicochemical properties that are similar to the reference synthetic hematite, goethite and aluminium hydroxide minerals. These prepared and well-characterized mineral well-plates are similar to naturally occurring surfaces in aquifers and enable us to study the different steps of bacterial adhesion and biofilm formation on these metal oxides under laboratory-controlled conditions.  相似文献   

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