Interphase migration and enrichment of lead and zinc during copper slag depletion

An interphase migration and enrichment model of lead and zinc during molten copper slag depletion was established.The occurrence of various components in copper slag was predicted using sulfur-oxygen potential calculations and confirmed through high-temperature experiments.The recovery rate of copper can reach 90.13%under the optimal conditions of 1200°C,an iron to silicon mass ratio of 1.0,3 wt.%ferrous sulfide,and a duration of 45 min.Lead(54.07 wt.%)and zinc(17.42 wt.%)are found in the flue dust as lead sulfate,lead sulfide,and zinc oxide,while copper matte contains lead(14.44 wt.%)and zinc sulfide(1.29 wt.%).The remaining lead and zinc are encapsulated as oxides within the fayalite phase.

Analysis of Oxygen Consumption in Lead and Zinc Metallurgy

This article analyzes the role of oxygen in lead zinc metallurgy,including shortening the metallurgical process,promoting energy conservation and environmental protection,improving metallurgical strength,enhancing raw material adaptability,and enhancing comprehensive recovery efficiency.This article introduces different lead zinc metallurgical processes and their oxygen consumption characteristics,including oxygen enriched side blowing lead smelting,oxygen bottom blowing lead smelting,oxygen enriched top blowing lead smelting,flash smelting lead,oxygen pressure leaching zinc smelting,and atmospheric pressure oxygen leaching zinc smelting.It is pointed out that oxygen enhanced metallurgy is the direction for the transformation and upgrading of lead zinc metallurgy.

Estimation of lead and zinc emissions from mineral exploitation based on characteristics of lead/zinc deposits in China

Nonferrous mining activities are some of the largest sources of heavy metals emissions into the environment and China is one of the largest producers and consumers of lead and zinc in the world.The cumulative productions and emissions of lead and zinc from mining-related activities in China were estimated.Up to 2007,the cumulative productions of lead and zinc in China were estimated to be about 6.69 and 12.59 Mt,respectively;and about 1.62 Mt lead and 3.32 Mt zinc emitted into the ambient environment during the mining,processing and smelting activities,representing 24.39% and 26.36% cumulative production,respectively.Among these three types of mining-related activities,mineral processing contributes the most to the total emission of 50.67% lead and 45.51% zinc.

Selective recovery of lead from zinc oxide dust with alkaline Na_2EDTA solution

The selective recovery of lead from the zinc oxide dust using an alkaline Na2EDTA solution was investigated. The effects of temperature, leaching time, Na2EDTA concentration and initial NaOH concentration on the leaching rates of lead and zinc were studied. The following optimized leaching conditions were obtained： liquid-to-solid ratio 5：1 mL/g, stirring speed 650 r/min, Na2EDTA concentration 0.12 mol/L, initial NaOH concentration 0.5 mol/L, leaching temperature 70 ℃, leaching time 120 min. Under the optimized conditions, the average leaching rates of lead, zinc, fluoride and chloride are 89.92%, 0.94%, 62.84% and 90.02%, respectively. The filtrate was used to electrowin lead powders. The average current efficiency of electrowinning is about 93% and lead content is higher than 98% under the conditions of temperature of 60 ℃, current density of 200 A/m2, H3PO4 concentration of 1.5 g/L, and lead ion concentration of above 5 g/L. The consumption of Na2EDTA and the direct current are about respectively 0.218 kg and 0.958 kW·h for per kilogram of lead powder.

Occurrence of lead and silver minerals and their interaction with xanthate in slurry of zinc electrolysis anode slime

The background pulp potential of zinc anode slime,and its influence on the occurrence of lead,silver and xanthate,were investigated with thermodynamic method.The thermodynamic conclusion and XRD analysis pointed out that in zinc anode slime,the thermodynamically stable compound of xanthate is dixanthogen,anglesite is the only mineral of lead,and kerargyrite is one of silver minerals occurring.Microflotation tests on single minerals of anglesite and kerargyrite in sulfuric acid solution by amyl dixanthogen indicated that dixanthogen has a much stronger collecting ability to kerargyrite than to anglesite.Molecular dynamic simulation indicated that amyl dixanthogen can only be adsorbed on the surface of kerargyrite in the presence of SO42-.The FTIR tests also verified the selective adsorption of amyl dixanthogen on the surface of kerargyrite in the presence of SO42-.

Effects of field application of phosphate fertilizers on the availability and uptake of lead, zinc and cadmium by cabbage (Brassica chinensis L.) in a mining tailing contaminated soil

A field trial was conducted to evaluate the reduction of bioavailability of heavy metals including lead (Pb), zinc (Zn) and cadmium (Cd) in a soil contaminated by mining tailings in Shaoxing, Zhejiang, China. Three commercial phosphate (P) fertilizers including phosphate rock (PR), calcium magnesium phosphate (CMP), and single superphosphate (SSP) were applied to the plot at three P application rates, 50, 300, and 500 g/m2 with 9 treatments and control (CK). Plants, water soluble and exchangeable (WE) extra...

Effects of Cadmium, Lead, and Zinc on Size of MicrobialBiomass in Red Soil

A laboratory incubation experiment was conducted to study the influence of cadmium (Cd), lead (Pb)and zinc (Zn) on the size of the microbial biomass in red soil. All the three metals were applied, separately,at five different levels that were: Cd at 5, 15, 30, 60 and 100 μg g-1; Pb at 100, 200, 300, 450 and 600 μg g-1 and Zn at 50, 100, 150, 200 and 250 μg g-1 soil. In comparison to uncontaminated soil, the microbial biomass carbon and biomass nitrogen decreased sharply in soils contaminated with Cd, Ph and Zn. A more considerable increase in the microbial biomass C: N ratio was observed in the metal contaminated soils than the non-treated control. Among the tested metals, Cd displayed the greatest biocidal effect followed by Zn and Pb, showing their relative toxicity in the order of Cd > Zn > Pb.

Sulfidation roasting of lead and zinc carbonate with sulphur by temperature gradient method

In order to enhance the lead and zinc recovery from the refractory Pb-Zn oxide ore, a new technology was developed based on sulfidation roasting with sulphur by temperature gradient method. The solid-liquid reaction system was established and the sulfidation thermodynamics of lead and zinc carbonate was calculated with the software HSC 5.0. The effects of roasting temperature,molar ratio of sulphur to lead and zinc carbonate and reaction time in the first step roasting, and holding temperature and time in the second roasting on the sulfidation extent were studied at a laboratory-scale. The experimental results show that the sulfidation extents of lead and zinc are 96.50% and 97.29% under the optimal conditions, respectively, and the artificial galena, sphalerite and wurtzite were formed. By the novel sulfidizing process, it is expected that the sulphides can be recovered by conventional flotation technology.

Sulphidization flotation for recovery of lead and zinc from oxide-sulfide ores

A new flowsheet was developed to recover the valuable minerals from oxide or oxide-sulfide ores of lead and zinc. The flowsheet consisted of flotation of sulfide minerals, desliming and sulphidization-flotation of oxide minerals. The corresponding reagent system and techniques to the flowsheet were investigated. Batch and continuous tests show that the dosage of sodium sulfide, temperature, and collector type are main affecting factors on the recovery of smithsonite and cerussite. For the flotation of cerussite, there is an appropriate dosage of sodium sulfide at which the recovery reaches its maximum value. The required sodium sulfide for smithsonite flotation is higher than that for cerussite and the recovery of smithsonite flotation increases with the dosage of sodium sulfide at low level and becomes insensitive at high dosage. The appropriate temperature for smithsonite and cerussite flotation is found to be 2540℃. Amines are found to be the effective collectors for the flotation of smithsonite after sulphidization. Investigation also shows that desliming prior to sulphidization-flotation is essential to the effective recovery of smithsonite and cerussite, and the desliming process of two-stage hydrocyclon is well feasible and effective for the treatment of lead-zinc oxide ores. A further treatment on the cerussite flotation concentrate by shaking table is proposed to obtain higher lead grade.

Leaching of lead from zinc leach residue in acidic calcium chloride aqueous solution

A process with potentially reduced environmental impacts and occupational hazards of lead-bearing zinc plant residue was studied to achieve a higher recovery of lead via a cost-effective and environmentally friendly process. This paper describes an optimization study on the leaching of lead from zinc leach residue using acidic calcium chloride aqueous solution. Six main process conditions, i.e., the solution pH value, stirring rate, concentration of CaC12 aqueous solution, liquid-to-solid （L/S） ratio, leaching temperature, and leaching time, were inves- tigated. The microstructure and components of the residue and tailing were characterized using scanning electron microscopy （SEM） and X-ray diffraction （XRD）. On the basis of experimental results, the optimum reaction conditions were determined to be a solution pH value of 1, a stirring rate of 500 r·min-1, a CaC12 aqueous solution concentration of 400 g·L-1, a liquid-to-solid mass ratio of 7：1, a leaching tempera- ture of 80℃, and a leaching time of 45 min. The leaching rate of lead under these conditions reached 93.79%, with an iron dissolution rate of 19.28%. Silica did not take part in the chemical reaction during the leaching process and was accumulated in the residue.

An experimental study on metal precipitation driven by fluid mixing: implications for genesis of carbonate-hosted lead–zinc ore deposits

A type of carbonate-hosted lead–zinc(Pb–Zn)ore deposits, known as Mississippi Valley Type(MVT)deposits, constitutes an important category of lead–zinc ore deposits. Previous studies proposed a fluid-mixing model to account for metal precipitation mechanism of the MVT ore deposits, in which fluids with metal-chloride complexes happen to mix with fluids with reduced sulfur, producing metal sulfide deposition. In this hypothesis, however, the detailed chemical kinetic process of mixing reactions, and especially the controlling factors on the metal precipitation are not yet clearly stated. In this paper, a series of mixing experiments under ambient temperature and pressure conditions were conducted to simulate the fluid mixing process, by titrating the metal-chloride solutions, doping withor without dolomite, and using NaHS solution. Experimental results, combined with the thermodynamic calculations, suggest that H_2S, rather than HS^-or S^(2-),dominated the reactions of Pb and/or Zn precipitation during the fluid mixing process, in which metal precipitation was influenced by the stability of metal complexes and the pH. Given the constant concentrations of metal and total S in fluids, the pH was a primary factor controlling the Pb and/or Zn metal precipitation. This is because neutralizing or neutralized processes for the ore-forming fluids can cause instabilities of Pb and/or Zn chloride complexes and re-distribution of sulfur species, and thus can facilitate the hydrolysis of Pb and Zn ions and precipitation of sulfides. Therefore, a weakly acidic to neutral fluid environment is most favorable for the precipitation of Pb and Zn sulfides associated with the carbonate-hosted Pb–Zn deposits.

Effect of Lead-Zinc Interaction on Size of Microbial Biomass in Red Soil

A laboratory incubation experiment was conducted to evaluate the effects of lead and zinc applied alone or in various combinations on the size of microbial biomass in a red soil. Treatments included the application of lead at six different levels i.e., 0 (background), 100, 200, 300, 450 and 600 μg g -1 soil along with each of the four levels of zinc (0, 50, 150 or 250 μg g -1 soil). Application of lead or zinc alone to soil significantly ( P <0.001) affected the soil microbial biomass. The microbial biomass carbon (C mic ), biomass nitrogen (N mic ) and biomass phosphorus (P mic ) decreased sharply in soils contaminated with lead or zinc. Combined application of lead and zinc resulted in a greater biocidal effect on soil microbial biomass, which was significantly higher ( P <0.001) than that when either lead or zinc was applied alone. Consistent increase in the biomass C:N and decline in the biomass C:P ratios were also observed with the increased metal (Pb and Zn) toxicity in the soil.

Investigation on the deactivation cause of lead-zinc double oxide for the synthesis of diphenyl carbonate by transesterification

The deactivation cause of lead-zinc double oxide for synthesis of diphenyl carbonate （DPC） by transesterification of dimethyl carbonate （DMC） with phenol has been investigated. X-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS）, infrared spectroscopy （IR）, thermogravimetry analysis （TG）, atomic absorption spectroscopy and elementary analysis are employed for the catalyst characterization. The results show that, the formation of Pb4O（OC6H5）6 through the reaction of phenol and lead species in the catalyst leads to the crystal phase change of active component and serious leaching of lead, which is the cause of the catalyst deactivation. In addition, the composition of the leached lead is ascertained to be a mixture of Pb4O（OC6H5）6 and PbO with the weight percentage of 62.7% and 37.3%, respectively.

Study on the response of wheat to lead, cadmium and zinc

The effect of lead, cadmium and zinc on the transcriptions and structures of 5 DNA fragments was studied by RNA slot blot hybridization and the analysis of restriction fragment length polymorphism (RFLP). The seeds of three wheat strains (Yunmai29, 1257, 5118) which had grown in contaminated area, Huize Lead Zinc Mine, Yunnan Province of China and in uncontaminated area were taken as the experimental materials. No obvious change of DNA structure was detected, but there were many differences in the DNA transcription levels. These results implied that lead, cadmium and zinc might inhibit DNA transcription and had much more effect on gene expression than structure in wheat, which might acclimate to metal pollution after having grown in pollution area for a long time and the interference of these metal ions in gene expression might be one of main mechanisms of metal toxicity and plant adaptation. The results also showed the microevolution of wheat in the lead zinc mine.

Isotopic Compositions of Sulfur in the Jinshachang Lead–Zinc Deposit, Yunnan, China, and its Implication on the Formation of Sulfur-Bearing Minerals

The Jinshachang lead-zinc deposit is mainly hosted in the Upper Neoproterozoic carbonate rocks of the Dengying Group and located in the Sichuan-Yunnan-Guizhou （SYG） Pb-Zn-Ag multi- metal mineralization area in China. Sulfides minerals including sphalerite, galena and pyrite postdate or coprecipitate with gangue mainly consisting of fluorite, quartz, and barite, making this deposit distinct from most lead-zinc deposits in the SYG. This deposit is controlled by tectonic structures, and most mineralization is located along or near faults zones. Emeishan basalts near the ore district might have contributed to the formation of orebodies. The j34S values of sphalerite, galena, pyrite and barite were estimated to be 3.6‰-13.4‰, 3.7‰-9.0‰, -6.4‰ to 29.2‰ and 32.1‰34.7‰, respectively. In view of the similar δ34S values of barite and sulfates being from the Cambrian strata, the sulfur of barite was likely derived from the Cambrian strata. The homogenization temperatures （T ≈ 134--383℃） of fluid inclusions were not suitable for reducing bacteria, therefore, the bacterial sulfate reduction could not have been an efficient path to generate reduced sulfur in this district. Although thermochemical sulfate reduction process had contributed to the production of reduced sulfur, it was not the main mechanism. Considering other aspects, it can be suggested that sulfur of sulfides should have been derived from magmatic activities. The δ34S values of sphalerite were found to be higher than those of coexisting galena. The equilibrium temperatures calculated by using the sulfur isotopic composition of mineral pairs matched well with the homogenization temperature of fluid inclusions, suggesting that the sulfur isotopic composition in ore-forming fluids had reached a partial equilibrium.

Recovery of zinc and lead from Yahyali non-sulphide flotation tailing by sequential acidic and sodium hydroxide leaching in the presence of potassium sodium tartrate

The recovery of zinc and lead from Yahyali non-sulphide flotation tailing using sulfuric acid followed by sodium hydroxide leaching in the presence of potassium sodium tartrate was experimentally investigated.In the acidic leaching stage,the effects of pH,solid-to-liquid ratio and temperature on the dissolution of zinc from the tailing were explored.82.3%Zn dissolution was achieved at a pH of 2,a temperature of 40°C,a solid-to-liquid ratio of 20%and a leaching time of 2 h,whereas the iron and lead dissolutions were determined to be less than 0.5%.The sulfuric acid consumption was found to be 110.6 kg/t(dry tailing).The leaching temperature had no beneficial effect on the dissolution of zinc from the tailing.The acidic leach solution was subjected to an electrowinning test.The cathode product consisted of 99.8%Zn and 0.15%Fe.In the alkaline leaching stage,the Pb dissolution increased slightly in the presence of potassium sodium tartrate.More than 60%of Pb was taken into the leach solution when the leaching temperature increased from 40 to 80°C.The final leach residue was analyzed by XRD and XRF.The XRD results indicated that the major peaks originated from the goethite and quartz while minor peaks stem from smithsonite and cerussite.The XRF analysis demonstrated that the residue contained 70.3%iron oxide.Based on the sequential leaching experiments,the zinc and lead were excellently depleted from the flotation tailing,leaving a considerable amount of iron in the final residue.

Alkaline leaching of metal melting industry wastes and separation of zinc and lead in the leach solution

In this work, a thorough examinations on the extractability of zinc and lead present in the steelmaking dusts using alkaline leaching process and the effectiveness of the zinc and lead separation in the resultant leaching solutions using sulfide precipitation method were made. It was found that only about 53% of zinc and over 70% of the lead could be leached out of the dusts, while the other 47% of zinc and 30% of lead were left in the leaching residues. The zinc and lead in the resultant leaching solution can be effectively and selectively separated. When the weight ratio of sodium sulfide (M.W. = 222-240) to Pb was kept at 1.8, the lead in the solution could be precipitated out quantitatively while all the zinc was remained in the solution. The zinc left in the solution can be further recovered by the addition of extra sodium sulfide with a weight ratio of sodium sulfide to the zinc over 2.6. The resultant filtrate can be recycled to the leaching of dust in the next leaching process.

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%.

The mechanisms of paragenesis and separation of silver, lead and zinc in hydrothermal solutions

On the basis of an experimental study and thermodynamic calculation, the mechanisms of paragenesis and separation of silver, lead and zinc in the hydrothermal system have been studied. At acidic to nearly neutral pH, their chloride complexes are stable, and among them the chloride complexes of zinc are most stable. And the sulfide complexes are the dominant species at nearly neutral to alkaline pH, while the sulfide complexes of silver are most stable. With decreasing temperature, , f-{O-2} and increasing pH, the solubilities of silver, lead and zinc will decrease, leading to their deposition and separation. For sulfide complexes, the concentrations of reduced sulfur and pH are two important factors affecting their stabilities. Complexes of different forms and stabilities respond to the variation of conditions to different extents, which gave rise to the paragenesis and separation of silver, lead and zinc in the whole ore-forming process of dissolution, transport and deposition.