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1.
The effects of oxidation potential (Eh) and zinc sulphate on the separation of chalcopyrite from pyrite were investigated at pH 9.0. The flotation recovery of these minerals is Eh dependent with maximum separation obtained at 275 mV SHE. Zinc sulphate addition improved this mineral separation at an Eh value of 275 mV by selectively depressing pyrite flotation. A different result was obtained at lower Eh values where zinc sulphate addition improved chalcopyrite flotation but had no or little effect on pyrite flotation. These opposite effects of zinc sulphate on mineral flotation were reconciled by examining the surface species of these minerals. The selective depression of pyrite flotation by zinc sulphate was also confirmed in the flotation of two copper ores.  相似文献   

2.
This paper discusses the selective depression of pyrite from chalcopyrite and arsenopyrite by biomodulation using Acidithiobacillus ferrooxidans under natural conditions of pH. The effect of bacteria–mineral interaction on the surface charge of mineral and bacterial cell was studied by microelectrophoresis. Adhesion experiments were conducted to establish the relationship between cell adhesion to specific minerals and the electrokinetic behaviour of the minerals subsequent to interaction with cells. Effect of bacterial interaction on the xanthate-induced flotation of all the minerals was assessed. Adhesion of A. ferrooxidans on pyrite was rapid and tenacious and subsequent to interaction with cells, pyrite remained hydrophilic even in presence of xanthate collector. The collector, on the other hand, was able to render good flotability to chalcopyrite even after interaction with bacterial cells. Copper activated arsenopyrite was able to retain its hydrophobicity in presence of cells due to poor attachment kinetics of cells to the mineral surface. Thus, by suitably conditioning with the cells and collector, it was possible to effectively depress pyrite from chalcopyrite and arsenopyrite.  相似文献   

3.
The flotation of chalcopyrite and sphalerite from copper and copper-zinc ores has been achieved without using thiol-type collectors. Typically, a sulfide ore sample is first treated with sodium sulfide either during grinding or during the preflotation conditioning period, and then the chalcopyrite is floated with frother alone. With a copper-zinc ore, sphalerite is subsequently floated from the chalcopyrite tailings by activating it with copper sulphate. Results of the collectorless flotation tests are comparable to those obtained by using thiol collectors. The mechanisms of selective collectorless flotation are discussed on the basis of differences in the solubilities of sulfide minerals.  相似文献   

4.
The rate of decomposition of potassium ethyl monothiocarbonate has been determined at pH values between 5 and 10, and its molar absorptivity at 221 nm determined to be 1.24 · 104mol/cm.A novel apparatus for use in the study of reactions between sulphide minerals, oxygen and thiol reagents has been developed, and applied to the reactions of potassium ethyl xanthate with galena and pyrite. It has been shown that both minerals react with ethyl xanthate in the presence of oxygen or oxidation products to form soluble as well as adsorbed xanthate derivatives. The soluble derivative has been identified to be ethyl monothiocarbonate. The adsorbed xanthate at a galena surface, unlike that at a pyrite surface, is gradually converted to a soluble monothiocarbonate under the action of dissolved oxygen. The effect of variables such as pH, the initial xanthate and oxygen concentrations, and the initial state of oxidation of the mineral on the formation of monothiocarbonate has been studied. It is tentatively proposed that an intermediate adsorbed mixed xanthate-hydroxide species is involved in the formation of monothiocarbonate at both galena and pyrite surfaces.The significance of the formation of monothiocarbonate to flotation practice is discussed briefly. The formation of monothiocarbonate represents a wastage of reagent, and could lead to a decrease in flotability of xanthated galena with time of exposure to aerated solutions.  相似文献   

5.
近年来,在相山铀矿田的西部牛头山地区深部发现了铅锌矿化体,其成因机制不明.为探讨牛头山铅锌矿化体物质来源,开展了硫化物原位硫同位素分析研究.根据硫化物矿物之间的充填和包裹关系判断,铅锌矿化体金属硫化物形成的先后顺序是:黄铁矿形成最早,方铅矿和闪锌矿次之,细脉状黄铜矿形成最晚.利用LA-MC-ICP-MS技术对矿化体中几种金属硫化物分别进行了系统的原位硫同位素分析.结果显示:黄铁矿、闪锌矿、方铅矿、细脉状黄铜矿的δ34S值介于-4.8‰~+5.4‰之间,各硫化物矿物之间硫同位素未达到完全平衡分馏,利用黄铁矿δ34S值得到的矿化流体δ34SΣS值(总硫同位素组成)近似为+3.7‰,与共生矿物对(闪锌矿-方铅矿)图解法得到的闪锌矿和方铅矿沉淀时矿化流体的δ34SΣS值(+3.2‰)相近,表明形成牛头山铅锌矿化体的矿化流体δ34SΣS值大约为+3.7‰,为岩浆硫.结合前人的岩浆岩年龄数据,我们判断该铅锌矿化体金属硫化物的硫可能主要来自次火山岩相花岗斑岩岩浆热液.同一薄片中闪锌矿δ34S值高于共生的方铅矿,表明两者硫同位素基本平衡,利用共生矿物对(闪锌矿-方铅矿)硫同位素温度计计算得出平衡温度为197~476℃,与前人通过脉石矿物流体包裹体得到的铅锌矿化流体温度基本一致.相山火山盆地与相邻的北武夷黄岗山、梨子坑等产铅锌矿的火山盆地具有相似的成矿条件及成矿物质来源,使相山火山盆地具有良好的铅锌多金属找矿前景.   相似文献   

6.
The suitability of a new reagent, Kr6D, as a depressant for galena and sphalerite in a differential sulphide flotation stage has been tested. Small-scale laboratory flotation tests on pure sulphide minerals indicated that the reagent is capable of depressing both galena and sphalerite when used in small doses. At higher concentrations, chalcopyrite is also depressed. Single-stage batch-scale flotation tests have been carried out on bulk sulphide concentrates containing the three sulphide minerals. Kr6D has been compared with starch as a depressant both in the presence and in the absence of sulphur dioxide. In each case the new modifier has been shown to be more effective. When using sodium dichromate as a differential depressant in similar tests, it has been shown that the quantity necessary to achieve selectivity between chalcopyrite and galena may be considerably reduced if small quantities of Kr6D are added.  相似文献   

7.
Minerals from deposits Chelopech, Elshitsa, Radka and Krasen have been studied and their gold contents determined by neutron-activation. In all deposits sulphide and sulphosalt minerals show a well-expressed ability to concentrate gold, although their role in individual deposits is not equal. The highest concentration of gold is in bornite, tennantite, enargite and the early generations of pyrite, chalcopyrite, galena and sphalerite. The low content of gold in the late generations of pyrite, chalcopyrite, galena and sphalerite is due to the process of recrystallization and redeposition. The data obtained show that gold has been extracted entirely from the solutions of the early quartz-pyrite stage mineralizations while during the later quartz-sulphosalt-sulphide and quartz-carbonite-sulphate stages it was only re-deposited and concentrated.  相似文献   

8.
通过对山东省平度市大庄子金矿区黄铁矿、方铅矿三个蚀变阶段特征研究,发现金矿化主要发生在第二阶段,强烈的石英-黄铁矿-碳酸盐化与金矿化的关系最为密切。金多数以包体的形式赋存于黄铁矿等金属硫化物中,并且在黄铁矿、方铅矿、闪锌矿等矿物共同产出时更有利于金的富集。研究认为石英和黄铁矿组合以及黄铁矿、黄铜矿、方铅矿、闪锌矿的组合可作为金的富集指示性矿物组合,伴生矿物之中方铅矿含金性最好。方铅矿、黄铜矿、闪锌矿和磁黄铁矿呈细脉状、网脉状、斑杂状产于含金石英脉和团块状黄铁矿的裂隙中,研究发现细脉状较团块状黄铁矿含金性要好。  相似文献   

9.
Calcite is generally associated with apatite minerals in phosphate deposits. To explore the possibility of separating these minerals by a soap flotation technique, their electrokinetic properties and flotation behaviour were studied in the presence of sodium oleate.Microelectrophoresis data indicate oleate adsorption on these minerals, and from Hallimond-tube flotation tests it has been noted that in a controlled pH environment and for a certain sodium oleate concentration range, separation of these minerals is possible.The study of apatite/calcite-sodium metasilicate-sodium oleate systems indicates the preferential adsorption of silicate at the calcite surface. This suggests the potential use of sodium metasilicate as the modifying agent for the separation of apatite from calcite by depressing calcite when using sodium oleate as collector.  相似文献   

10.
The Pojeonri Cu quartz veins occur in the north-western portion of the Hwanggangri Metallogenic Province and consist of two parallel massive quartz veins that fill fractures oriented NW and NE along fault zones in Paleozoic metasedimentary and sedimentary rocks of the Ogcheon and Taebaeg belts. Based on the mineralogy and paragenesis of the veins, only one mineralization episode has been recognized. The ore minerals are mainly chalcopyrite, pyrrhotite, and pyrite with minor arsenopyrite, sphalerite, galena and oxides of those base metal minerals.  相似文献   

11.
云南官房铜矿床矿石矿物特征及银的赋存状态   总被引:1,自引:0,他引:1  
通过显微镜鉴定、电子探针(EPMA)及扫描电镜能谱分析(SEM/EDS)等方法,首次对官房铜矿的矿物组合和银的赋存状态进行了研究。初步查明,矿石矿物为中-低温热液成因,并受火山机构及断裂构造的控制;银矿物主要为碲银矿和辉银矿。矿石中银与铜呈明显正相关关系,而方铅矿中不含银。银主要以类质同象的形式赋存于含铜矿物或黄铁矿中;银的独立矿物含量低,且多呈包裹体的形式存在于黄铜矿、斑铜矿及黄铁矿中,或以微细粒状赋存于矿物颗粒间和斑铜矿的表面。  相似文献   

12.
The Okinawa Trough is characterized by enrichment of Ag in hydrothermal precipitates; however, the distribution of this enrichment remains poorly constrained. This study presents the results of a field-emission scanning electron microscopy and electron-microprobe analysis based mineralogical and geochemical investigation of the spatial distribution of Ag within Ag-rich sulfide samples from the Okinawa Trough. The tetrahedrite, covellite, and galena in these samples contain high concentrations of Ag(average values of 1.60, 0.78, and 0.23 wt%, respectively) and also various Ag sulfosalts. Examination of the Ag budget of these samples indicates that most of the Ag is hosted by tetrahedrite followed by galena. The Ag within tetrahedrite is incorporated by substitution into the Cu site, whereas galena becomes Ag-enriched by the coupled incorporation of monovalent Ag, Tl, and Cu, and trivalent Sb and Bi into Pb lattice sites. Tetrahedrite and galena containing higher concentrations of Sb favor increased Ag substitution. Four sets of Ag host minerals are identified with distinct ore formation temperatures. Tetrahedrite and galena concentrate the majority of Ag at medium temperatures(150–300°C). Other Ag host minerals concentrate only minor or trace amounts of Ag, including massive sphalerite, chalcopyrite, and pyrite at high temperatures(300°C), colloform pyrite and sphalerite at low temperatures(150°C), and Ag-sulfosalts at even lower temperatures(100°C).  相似文献   

13.
The Ohori deposit, one of the base metal deposits in the Green-Tuff region, NE Japan, is composed of two types of mineralization; a skarn-type (Kaninomata orebody) made by the replacement of the Miocene calcareous layer, and a vein-type (Nakanomata orebody). While the ore mineral assemblage of the deposit (chalcopyrite, pyrite, sphalerite and galena) has been known for being rather simple, some Pb-Bi-S minerals have been discovered for the first time in the present study. The minerals mainly occur in the chalcopyrite-rich ores of both orebodies. They essentially belong to the Pb-Bi-S system and contain Cu and Ag in minor amounts, which correspond to the lillianite–gustavite solid solution series (phases Z and X), cosalite, neyite, felbertalite, krupkaite and Bi-bearing galena. The chalcopyrite-rich (Bi-bearing) ores from both orebodies are richer in chalcopyrite, pyrite and chlorite, and have higher homogenization temperatures (>300°C) of fluid inclusions, and higher FeS contents in sphalerite compared to the Bi-free ores. In the Green-Tuff region, Bi-minerals have been reported from many base metal deposits. Most of these Bi-bearing ore deposits are referred to as xenothermal-type deposits, and are characterized by the following common features; composite mineralization of high- and low-temperatures in the shallower environments, and close relationships with the Tertiary granitic rocks. The whole mineralization at the Ohori deposit also has a similar xenothermal character because of the coexistence of high-temperature chalcopyrite-rich ores with Pb-Bi-S minerals, which were formed by the influence of the Tertiary granitic rocks at a shallow depth.  相似文献   

14.
周丽  李和平  徐丽萍 《矿物岩石》2006,26(1):110-115
金属硫化物矿物之间的原电池反应对于酸性矿山排水的形成、硫化物矿床的次生富集作用、地球电化学勘探以及湿法冶金过程等都有很重要的影响。通过改变溶液中氧化剂组分F e3 的浓度、pH值、溶液的流动状况以及溶液的盐度(如N a2SO4的浓度),采用精密的电流计和电位计,对作为阳极的黄铁矿与作为阴极的方铅矿所形成的原电池反应的电流密度和整个原电池的混合电位进行研究,结果表明:溶液中[F e3 ],pH值以及溶液的流动状况对黄铁矿和方铅矿之间原电池反应的影响很大,而溶液的盐度对反应的影响不是很显著。实验还发现,当黄铁矿电极表面存在微小裂纹时,其电极电位可降低至同条件下方铅矿的电极电位以下。这一实验结果在混合电位理论和Bu tler-V o lm er方程中得到了理论上的解释。  相似文献   

15.
A system is presented in which an atmosphere containing less than 10?6 mole fraction oxygen and water containing less than 5 ppb oxygen can be maintained. Flotation of chalcocite, chalcopyrite, galena, pyrite and sphalerite in this system reveals that these minerals are naturally floatable under these conditions.  相似文献   

16.
The flotation of < 10, 10–20, and 20–40 μm galena fractions was studied. For uncleaned galena a given collector coverage produced better floatability with increasing grain size. Nitrogen had a detrimental effect only for the < 10 μm fraction, producing at a given collector coverage a recovery smaller than that obtained with air.Galena cleaned with 400 g/l ammonium acetate had very poor floatability, although xanthate abstraction was fairly high; this confirms that strong xanthate adsorption is necessary for flotation. Formation of monothiocarbonate was small in all cases, which points to a very minor influence, if any, of this compound in the flotation process.In blank flotation tests, or for very low residual xanthate concentrations, a peak at 208 nm and a shoulder at 255 nm were observed. The former was assigned to the uncomplexed Pb2+ ion, and the latter was tentatively attributed to the PbOH+ ion.Lead in solution results from dissolution of the oxidation products of galena, as galena itself has an exceedingly low solubility. The curve for total lead in solution vs. initial xanthate concentration, had a minimum for an initial xanthate concentration of 10?5M, the further increase in dissolved lead is attributed to formation of complexes such as PbX+ (X = xanthate). Dissolved lead concentrations were nearly as high for cleaned as for uncleaned galena, which indicates a high oxidation rate of the mineral.  相似文献   

17.
34S/32S ratios have been measured in a suite of samples from the stratabound, volcanogenic massive sulphide deposit at Woodlawn, N.S.W. 34S values for the sulphides vary as follows: in the ore horizon, pyrite +6.7 to +9.2%. (mean +8.1‰), sphalerite +5.2 to +8.6‰. (mean +6.9‰), chalcopyrite +6.4 to +7.0‰ (mean +6.7‰) and galena +2.8 to +5.5‰ (mean +4.4‰); in the vein mineralization, the host volcanics—pyrite +8.7 to +11.4%. (mean +9.8‰), sphalerite +7.8 to + 10.3‰ (mean +9.2‰), chalcopyrite; +8.8 to +10.1‰ (mean +9.2‰) and galena +6.9 to +7.2‰ (mean +7.1‰). Barite from the upper ore horizon levels has an isotopic composition of +30.0‰, consistent with its having originated from Silurian ocean sulphate. The general order of 34S enrichment in the sulphides is pyrite > chalcopyrite sphalerite > galena. Isotopic fractionations in the systems galena/sphalerite/pyrite and chalcopyrite/pyrite indicate an equilibration temperature of 275–300°C. This temperature is considered to represent that of sulphide deposition.  相似文献   

18.
Mineral assemblages, chemical compositions of ore minerals, wall rock alteration and fluid inclusions of the Gatsuurt gold deposit in the North Khentei gold belt of Mongolia were investigated to characterize the gold mineralization, and to clarify the genetic processes of the ore minerals. The gold mineralization of the deposit occurs in separate Central and Main zones, and is characterized by three ore types: (i) low‐grade disseminated and stockwork ores; (ii) moderate‐grade quartz vein ores; and (iii) high‐grade silicified ores, with average Au contents of approximately 1, 3 and 5 g t?1 Au, respectively. The Au‐rich quartz vein and silicified ore mineralization is surrounded by, or is included within, the disseminated and stockwork Au‐mineralization region. The main ore minerals are pyrite (pyrite‐I and pyrite‐II) and arsenopyrite (arsenopyrite‐I and arsenopyrite‐II). Moderate amounts of galena, tetrahedrite‐tennantite, sphalerite and chalcopyrite, and minor jamesonite, bournonite, boulangerite, geocronite, scheelite, geerite, native gold and zircon are associated. Abundances and grain sizes of the ore minerals are variable in ores with different host rocks. Small grains of native gold occur as fillings or at grain boundaries of pyrite, arsenopyrite, sphalerite, galena and tetrahedrite in the disseminated and stockwork ores and silicified ores, whereas visible native gold of variable size occurs in the quartz vein ores. The ore mineralization is associated with sericitic and siliceous alteration. The disseminated and stockwork mineralization is composed of four distinct stages characterized by crystallization of (i) pyrite‐I + arsenopyrite‐I, (ii) pyrite‐II + arsenopyrite‐II, (iii) galena + tetrahedrite + sphalerite + chalcopyrite + jamesonite + bournonite + scheelite, and iv) boulangerite + native gold, respectively. In the quartz vein ores, four crystallization stages are also recognized: (i) pyrite‐I, (ii) pyrite‐II + arsenopyrite + galena + Ag‐rich tetrahedrite‐tennantite + sphalerite + chalcopyrite + bournonite, (iii) geocronite + geerite + native gold, and (iv) native gold. Two mineralization stages in the silicified ores are characterized by (i) pyrite + arsenopyrite + tetrahedrite + chalcopyrite, and (ii) galena + sphalerite + native gold. Quartz in the disseminated and stockwork ores of the Main zone contains CO2‐rich, halite‐bearing aqueous fluid inclusions with homogenization temperatures ranging from 194 to 327°C, whereas quartz in the disseminated and stockwork ores of the Central zone contains CO2‐rich and aqueous fluid inclusions with homogenization temperatures ranging from 254 to 355°C. The textures of the ores, the mineral assemblages present, the mineralization sequences and the fluid inclusion data are consistent with orogenic classification for the Gatsuurt deposit.  相似文献   

19.
对云南、海南、江西、湖北、河南、新疆、浙江、山东、辽宁等27个省185个典型金矿床的自然重砂矿物进行统计分析,发现自然重砂矿物对金矿具有良好的响应,自然金、黄铁矿、方铅矿、黄铜矿、白铅矿、辰砂等对寻找金矿具有指示意义。不同成因类型的金矿床反映出的自然重砂矿物组合不同,斑岩型金矿床的标型指示矿物组合为自然金+黄铁矿+方铅矿+重晶石+闪锌矿+白铅矿+金红石,卡林型—类卡林型金矿床的标型指示矿物组合为自然金+黄铁矿+方铅矿+辉锑矿+毒砂+雄(雌)黄,而造山型+矽卡岩型+热液型+构造蚀变岩型金矿床的标型指示矿物组合为自然金+黄铁矿+方铅矿+辰砂。不同区域的金矿床反映出的自然重砂矿物组合也各有差异,闪锌矿为南方各省金矿床的特征矿物,辰砂和白钨矿为北方地区金矿床的特征矿物,重晶石和白铅矿为西部地区金矿的特征矿物。综合研究认为,自然重砂具有直接找矿和指导找矿的作用,按照特定成因类型和区域金矿床所建立的自然重砂矿物组合对建立矿床找矿模型具有重要的意义。  相似文献   

20.
通过野外及镜下研究,初步查明丁家林,太阳坪金矿区所含金矿物为自然,金金矿及含银自然金。丁家林金矿区包裹体金为主,太阳坪金矿区则以裂隙金为主。粒数及面积统计显示两矿区均以中、细粒金为主。载体矿物主要为黄铁矿,次为石英,偶见方铅矿,黄铜矿及闪锌矿。金的矿化与富集以富含黄铁矿,贫其他多金属硫化物为特征。矿石中常见明金为粗粒金,巨粒金及块状金。  相似文献   

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