硫化矿物的浮选电化学与浮选行为

研究黄铜矿、黄铁矿、方铅矿等矿物在有/无捕收剂两种情况下的浮选行为,考察浮选与矿浆电位的关系。结果表明:当pH值分别小于4.0时,黄铜矿无捕收剂浮选的电位区间为0~0.9 V;当pH值为4.0或11.0时,矿浆电位大于0.85 V以后,黄铁矿的浮选回收率低于20%;当pH值为11.0时,黄铜矿无捕收剂浮选的矿浆电位区间为0.35~0.85 V。当pH值为10.0、丁黄药浓度为5×10-5 mol/L时,方铅矿浮选的矿浆电位为0.45~0.55 V,而黄铜矿在0.45~0.80 V的电位区间具有良好的浮选性能;对闪锌矿而言,当pH值为9.0时,矿浆电位在-0.40~0.80 V区间都不具有良好的可浮性。在浮选体系中,黄铜矿表面氧化会产生元素S0,当矿浆电位从-0.2V增大至0.6 V,黄铜矿表面氧化产生的元素S的数量逐渐增大,黄铜矿的无捕收剂浮选性能越来越好。从南京和青海2个铅锌矿山的应用情况来看,采用电位调控浮选技术可以大幅度缩短铅矿石的浮选时间,减少浮选机数量。例如在南京某铅锌矿,由于采用电位调控浮选技术,原来2个系列每天处理900 t矿石,现在采用一个系列即可处理。     

Electrochemical flotation of ethyl xanthate-pyrrhotite system

1　INTRODUCTIONPyrrhotite(Fe1-xS ,0 相似文献   

Flotation separation of marmatite from pyrrhotite using DMPS as depressant

1 Introduction Pyrrhotite and marmatite are found in most sulfide ore bodies together. Their separation becomes an important issue. In the flotation of complex sulfide ores, high pH value is generally used to separate valuable sulfide minerals from pyrrh…     

使用抑制剂甘油基黄原酸钠浮选分离铁闪锌矿与黄铁矿(英文)

研究抑制剂甘油基黄原酸钠(SGX)在铁闪锌矿与黄铁矿浮选分离过程中的作用机理。通过浮选实验考察该抑制剂对硫化矿物的浮选抑制行为。结果表明,用丁黄药作捕收剂,在SGX存在下铁闪锌矿能被Cu2+活化从而具有良好的可浮性,而黄铁矿不能被Cu2+活化;在pH为4-11的范围,SGX的用量小于50mg/L时,可以实现两种矿物的选择性分离。动电位分析表明,SGX在Cu2+存在的条件下不能阻止丁黄药的阴离子在铁闪锌矿表面的吸附,但能阻止丁黄药的阴离子在黄铁矿表面的吸附。吸附等温测试结果表明,SGX在黄铁矿表面的吸附量远比在铁闪锌表面量大。     

Electrochemical oxidation of pyrrhotute in aqueous solution

The anodic surface oxidation of natural pyrrhotite in 0.3 mol/L KCI and HCI solution （pH 4.0） and 0.1 mol/L Na2B4O7 solution （pH 9.18） respectively was investigated by using cyclic voltammetry, Tafel plot, and chronoamperometry. In 0.3 mol/L KCl and HCl solution （pH 4.0）, at potential less than 0.5 V（vs SHE）, the production of anodic oxidation on pyrrhotite surface can not maintain a stable phase to form a passive film. In 0.1 mol/L Na2B4O7 solution （pH 9.18）, when the electrode potential increases to more than 0.5 V （vs SHE）, part of S is oxidized to sulfate, making the passive film somewhat porous, but elemental S and metal oxidates Fe（OH）3 still remain on the electrode surface, and the passive film can not be broken down totally. According to PARCalc Tafel analysis, the corresponding corrosion current density （J0） is 5.34 μA/cm^2 , which is also the exchange current density of the oxidation reaction on pyrrhotite electrode surface in 0. 1 mol/L Na2B4O7 solution （pH 9. 18）. The electrochemical dynamics equation of the oxidation was determined.     

Improvement of flotation behavior of Mengzi lead-silver-zinc ore by pulp potential control flotation

The electrochemical behavior of Mengzi lead-silver-zinc ore flotation system was studied. Based on the electrochemical characteristics of sulfide mineral flotation system, a stage potential control flotation was developed with the main parameters of pulp potential（φp）, pH value and collector dosage. Using N,N＇ diphenylamino-dithiolphosphoric acid（NNDDC） as a collector, which has good selectivity for galena flotation at pH 8.8 and pulp potential 330 mV, DDTC is used as secondary collector to improve both the grade and recovery of Pb and Ag. The pulp potential values significantly influence the floatability of practical minerals and single minerals when using NNDDC as the collector. The flotation recovery of galena reaches 85% at about 0.3 V and pH8.8. With the usage of pulp potential control during grinding and flotation, the new pulp electrochemical technology for Mengzi lead-silver-zinc ore flotation was developed. The results show that the grades of Pb and Ag of galena concentrate are 55% and 1 800 g/t, respectively, while the recoveries of Pb and Ag are 86.5% and 65%, respectively, the grade of Zn of marmatite concentrate is 42.5%, and the recovery of Zn is 91.25%.     

铁闪锌矿的浮选行为及其表面吸附机理

通过浮选实验和红外光谱测定, 考查了铁闪锌矿在无捕收剂或以乙黄药为捕收剂时的浮选行为.结果表明: 铁闪锌矿在酸性条件下, 可实现无捕收剂浮选, 硫酸铜的活化效果不明显; 在乙黄药体系下, 铁闪锌矿只能在酸性条件下可浮, 表面生成产物主要为乙黄原酸锌; 但有硫酸铜存在时, 铁闪锌矿可浮性得到大大改善, 当硫酸铜用量达到一定程度, 在整个pH值范围内铁闪锌矿均有较好的可浮性, 铁闪锌矿表面生成物为CuEX.     

铁闪锌矿的腐蚀电化学研究

采用Tafel曲线、交流阻抗法，研究了铁闪锌矿与浮选药剂相互作用的界面电化学行为．结果表明：pH对铁闪锌矿的腐蚀电位几乎无影响，但随着pH增大，腐蚀电流增大，矿物表面的疏水性元素S^0急剧减少，羟基化作用变大；二乙基二硫代氨基甲酸钠是铁闪锌矿的腐蚀剂和浮选抑制剂，Ca(OH)2在成本和性能上，都是碱性浮选介质中最佳的pH调整剂．     

Marmatite bioleaching with moderately thermoacidophilic bacterial strain and mineral analyses of solid residues

The bioleaching of a marmatite flotation concentrate with a moderately thermoacidophilic iron-oxidizing bacterial strain （MLY） is influenced significantly by temperature, pH, particle size, pulp density of ores and bacterial strains. Under such leaching conditions as the initial pH value of 1.5, temperature of 50℃, pulp density of 5%, particle size less than 35.5μm （over 90%） and inoculating the adapted strains of MLY, the leached Zn is over 95% after 10 d of bioleaching. SEM observations show the cell attachment and the surface features of solid residues under different leaching conditions. XRD and EDX analyses show that a mass of elemental sulfur form during the bioleaching process. The technological feasibility of a microbiological process using MLY for extracting zinc from the marmatite concentrate is demonstrated.     

Bio-oxidation of arsenopyrite

Oxidation of arsenopyrite with Acidithiobacillus ferrooxidans was studied. The electrochemical results show that arsenopyrite is firstly oxidized to As2S2 at the potential of 0.2-0.3 V （vs SHE） and As2S2 covers the electrode and retards the process continuously. While at higher potential over 0.3 V （vs SHE）, AszS2 is oxidized to H3AsO3, and H3AsO3 is then oxidized to H3AsO4 at 0.8 V （vs SHE）. The leaching results show that the addition of FeS2 can promote the oxidation of As^3＋ to As^5＋ and increase the activity of the bacteria. The best bio-oxidation technical parameters are the initial pH of 1.8-2.0, particle sizes less than 0.074 mm, temperature in the range of 25-30℃ and rotating speed of the orbital incubator of 100-160 r/min. The results provide theoretical and technological supports of bio-oxidation arsenopyrite for pretreating refractory arsenic gold ores.     

Effect of Cu~(2+)ions on bioleaching of marmatite

The effect of Cu~(2+)ions on bioleaching of marmatite was investigated through shake leaching experiments.The bacteria inoculated are a mixed culture ofAcidithiobacillus ferrooxidans,Acidithiobacillus thiooxidans and Lepthospirillum ferrooxidans.The results show that zinc is selectively leached,and the addition of appropriate content of Cu~(2+)ions has positive effect on the bioleaching of marmatite.SEM and EDX analyses of the leaching residue reveal that a product layer composed of iron sulfide, element...     

FTIR spectroscopic study of electrochemical flotation of jamesonite-diethyldithiocarbamate system

1 Introduction Flotation electrochemistry and modern surface analytical techniques have enhanced our understanding of reagent-mineral interaction mechanism. Great progress has been made by applying various electrochemical techniques to investigate the int…     

Floc flotation of marmatite fines in aqueous suspensions induced by butyl xanthate and ammonium dibutyl dithiophosphate

The hydrophobic flocculation of marmatite fines in aqueous suspensions induced by butyl xanthate (KBX) and ammonium dibutyl dithiophosphate (ADD) was investigated using laser particle size analysis, microscopy analysis, electrophoretic light scattering, contact angle measurement and infrared spectroscopy. The studies were performed on single minerals with size ≤20 µm by varying several parameters, including pH, collector concentration and kerosene addition. The results show that the floc flotation closely correlated with the size of flocs and the particle hydrophobicity, but was not lowered with increasing the particle surface charges due to collector adsorption. Under good operating conditions, the floc flotation of marmatite fines as a function of KBX and ADD can all reach floatability over 90%, in comparison with conventional flotation obtaining floatability of about 60%. It also has been found that a small addition of kerosene greatly improved the floc flotation because of the formation of oil films on marmatite particles. The results of FTIR spectra indicate that adsorption of the two collectors onto marmatite were chemical adsorption.     

钛渣中钙钛矿的浮选分离及其机理

研究了捕收剂油酸、羟肟酸、十二烷胺双甲基膦酸 ,抑制剂氟硅酸钠、水玻璃对改性渣中钙钛矿浮选的影响。通过浮选溶液化学计算、矿物动电电位、红外光谱等研究 ,探讨了羟肟酸在钙钛矿表面的作用和水玻璃抑制钛辉石的作用机理。结果表明 :以羟肟酸为捕收剂 ,水玻璃为抑制剂可实现钙钛矿与钛辉石等的浮选分离。钙钛矿和钛辉石晶体表面的Ca,Ti质点密度不同 ,所处的位置及活性不同 ,造成二者浮游性有一定的差异 ;钙钛矿在整个研究范围内 ζ电位始终为负值 ,但在阴离子捕收剂C5-9羟肟酸中可浮性良好 ,表明C5-9羟肟酸在钙钛矿表面发生了化学吸附。红外光谱研究证实 ,C5-9羟肟酸的CN ,N—O官能团与钙钛矿表面的钛质点发生了化学键合。     

金属阳离子在锂辉石浮选中的活化行为及作用机理

在油酸浮选锂辉石体系中分别加入Ca^2+、Al^3+、Fe^3+离子,通过单矿物浮选试验、金属离子吸附量检测、金属离子水解组份浓度计算、矿物表面动电位测试、红外光谱检测以及量子化学模拟计算研究Ca^2+、Al^3+、Fe^3+离子对锂辉石浮选的活化行为和作用机理。结果表明:Ca^2+离子的最佳活化区间为pH大于12的强碱性条件,Al^3+离子的最佳活化pH为6.47,而Fe^3+离子的最佳活化pH为7.25;在这些pH区间内,锂辉石浮选回收率和金属离子吸附量均达到最大值。在锂辉石浮选过程中起活化作用的有效组份为它们分别对应的氢氧化物沉淀。Ca^2+、Al^3+、Fe^3+离子可使锂辉石表面动电位向正值方向显著偏移;Ca^2+离子在锂辉石表面双电层的外层发生静电吸附,Al^3+和Fe^3+离子在锂辉石表面双电层的内层发生特性吸附。钙原子与锂辉石矿物表面吸附后形成的Ca—O键的键强较小,以离子键为主;铁原子与矿物表面形成Fe—O化学键的键强较大,含有一定的共价键组份;而铝原子与矿物表面吸附后形成的Al—O键的键长、键强等参数介于钙、铁的参数之间。油酸在Ca^2+活化后的锂辉石表面发生了化学吸附和少量的物理吸附,而在Al^3+、Fe^3+活化后的锂辉石表面发生了较为强烈的化学吸附。     

Collectorless flotation of marmatite with pine oil

The interaction between pine oil and marmatite without collectors and activators was investigated by flotation,scanning electron microscope and energy-dispersive spectrometer(SEM-EDS),infrared(IR) spectroscopy,Zeta potential,and first-principle theory calculations.The flotation results show that marmatite exhibits considerable floatability with the addition of pine oil.SEM-EDS results show that carbon atomic ratios on the surface are significantly high,which suggests that the flotation of marmatite is caused by the adsorption of pine oil.Further evidence of the adsorption mechanism was given by IR,and Zeta potential examining pine oil depends on the physical adsorption on the surface independently.The first-principle theory calculations indicate that pine oil molecule adsorbs on Zn and Fe atom surfaces by ionic bond and covalent bond of adsorption energies of-1.23and-1.51 eV,respectively.P orbital of O atom,s orbital of Zn atom,and d orbital of Fe are the major participants.     

Flotation Behavior and Mechanism of Anglesite with Salicyl Hydroxamic Acid as Collector

The flotation behavior of anglesite at different pulp pH levels was studied, with salicyl hydroxamic acid (SHA) acting as collector. The results demonstrated the effectiveness of SHA over a wide pH range. Zeta potential, adsorption, and x-ray photoelectron spectroscopy measurements were carried out to explore the interactions between SHA and anglesite. The results showed that the adsorption of SHA on the surface of anglesite was both chemical and physical. Furthermore, experiments with a bench-scale closed-flotation circuit proved that the collector can effectively recover anglesite from zinc-leaching residues (ZLRs). This work sheds new light on flotation of anglesite, providing a significant contribution to understanding of anglesite flotation and its application for disposal of ZLRs.     

金属离子强化铁闪锌矿浮选精矿的生物浸出

考察了金属离子Cu2 、Fe3 和Fe2 等对铁闪锌矿浮选精矿生物浸出的影响,并与无菌条件下对铁闪锌矿浸出的影响进行比较.结果表明:Cu2 、Fe3 和Fe2 等金属离子在一定浓度范围内都可以促进铁闪锌矿的生物浸出;在无菌条件下,除Fe2 外,Cu2 和Fe3 离子仍对铁闪锌矿溶解有一定的促进作用.电化学测试和X射线衍射分析表明:添加Cu2 和Fe3 等离子将影响铁闪锌矿电极发生的电化学反应和浸渣组成;添加Cu2 离子可取代矿物基质晶格中的Zn而生成CuS沉淀,并与锌矿产生原电池效应而促进浸出过程;Fe3 和Fe2 两种离子强化铁闪锌矿生物浸出的机理本质上一致,均可以提高浸出液中氧化剂浓度和促进细菌生长与生物活性.     

Flotation of indium-beard marmatite from multi-metallic ore

Flotation of indium-beard marmatite from Dulong multi-metallic ore in Yunnan Province of China was studied to improve the grades and recoveries of zinc and indium of the zinc concentrate in Dulong concentration plant.The experimental results indicated that copper sulfate mixed with a chemical reagent X-1 as the activator in the marmatite flotation produced a much better beneficiation than copper sulfate alone,increasing the zinc and indium recoveries of 10% and 6%,respectively,while the concentrate grades remained unchanged.Also,the new activator acted well around pH 10,allowing large savings on lime consumption in the rnarmatite flotation.In addition,it has been found that a sufficient activated lime of activator with ore slurry in the flotation is needed to achieve good beneficiation of the marmatite ore.     

Selective depression of copper-activated sphalerite by polyaspartic acid during chalcopyrite flotation

Environmentally friendly flotation reagent, polyaspartic acid (PAPA), was tested as a potential selective depressant in the flotation separation of chalcopyrite and Cu-activated sphalerite. The depression mechanism of PAPA was revealed by contact angle measurements, Zeta potential measurements, Fourier transform infrared spectroscopy (FT-IR) analysis and inductively coupled plasma (ICP) measurement. The micro-flotation tests with single minerals showed that PAPA selectively depressed Cu-activated sphalerite, while chalcopyrite remained floatable. Moreover, a concentrate containing 31.40% Cu with a recovery of 92.43% was obtained in flotation tests of artificially mixed minerals. Results of contact angle measurements, Zeta potential measurements and FT-IR spectrum revealed that PAPA exerted a much stronger adsorption on Cu-activated sphalerite surface than on chalcopyrite surface, preventing the further adsorption of sodium diethyl dithiocarbamate (DDTC) on its surface. ICP measurements indicated that PAPA had an excellent complexing ability with Cu²⁺ in flotation pulp, weakening the activation of Cu species on sphalerite surface and producing selective depression.