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By John O. Marsden

The past fifteen years have seen a number of important developments in copper hydrometallurgy, including the commercial application of biological heap leaching of secondary (chalcocite-dominant) copper ores, the commercial demonstration of chalcopyrite concentrate leaching technology using pressure leaching and biological processes, and the application of novel configurations of solution extraction circuits. Significant emphasis is now being placed on the development of effective stockpile leaching practices for primary ores (chalcopyrite and bornite-dominant mineralization). Some of these developments have been highly successful, and will pave the way for further development and commercialization. Others have been less successful. These developments are reviewed in the context of the metal price cycle and trends for the future are identified.

Jan 1, 2006

By John O. Marsden

The past fifteen years have seen a number of important developments in copper hydrometallurgy, including the commercial application of biological heap leaching of secondary (chalcocite-dominant) copper ores, the commercial demonstration of chalcopyrite concentrate leaching technology using pressure leaching and biological processes, and the application of novel configurations of solution extraction circuits. Significant emphasis is now being placed on the development of effective stockpile leaching practices for primary ores (chalcopyrite and bornite-dominant mineralization). Some of these developments have been highly successful, and will pave the way for further development and commercialization. Others have been less successful. These developments are reviewed in the context of the metal price cycle and trends for the future are identified.

Jan 1, 2006

By Funsho K. Ojebuoboh

With several "green" applications in the horizon, bismuth has become an even more important minor metal in the smelting and refining of lead. Smelters with a complex sulfide feed invariably deal with bismuth. Its behavior during the smelting of lead in conventional sinter - blast furnace operation is discussed. Because it readily deports to the lead phase during the refining of lead, its separation from refined lead remained unsatisfactory in early lead production. When commercial requirements of bismuth in lead became more stringent early this century, the procedure whereby calcium and magnesium is used to debismuthise lead was developed. The present conduct of this 1936 process, the Kroll Betterton process, is discussed with emphasis on operational improvements.

Jan 1, 1995

By Keith Axler

The high reactivity of plutonium metal presents safety concerns related to material containment during fire scenarios. Plutonium metal is liquid at temperatures achieved under selected fire scenarios. The appearance of liquid plutonium challenges the corrosion resistance of the containment materials. However, by the in situ formation of intermetallic compounds, the plutonium metal can be stabilized as solid and the integrity of the containment vessels preserved. Studies have been conducted to demonstrate candidate materials, including lead, which can be introduced to the liquid-plutonium system and bind the corrosive liquid metal through the formation of intermetallic phases. The results of these investigations will be presented along with a discussion of the experimentally determined phase behavior for the plutonium-lead system.

Jan 1, 1995

By Bernard Bonnetot

The potentialities of hydrogen storage using borohydrides are presented and discussed especially in regard to the recoverable hydrogen amount and to the recovery conditions. A rapid analysis of storage possibilities is proposed taking in account the two main ways for hydrogen evolution: the dehydrogenation obtained using thermal decomposition of borohydrides or the hydrolysis of solid or dissolved borohydrides. The recoverable hydrogen is related to the dehydrogenation conditions and the real hydrogen useful percentage is determined for each case of use. The high temperatures required for dehydrogenation, even using catalyzed borohydrides, lead to poor outlooks for this storage technique. The hydrolysis conditions fix the yield of the recovered hydrogen and rule the storage capacity of the dissolved borohydride, the "fuel".

Jan 1, 2006

By Christian Ludwig, Virginie Silberstein, Rizlan Bernier-Latmani, Simona Regenspurg

"Residues from waste incineration (bottom ashes) form large amounts of heavy metal-rich waste. Theoretically, heating and the addition of chloride to the ashes could remove these metals by formation of volatile metal chlorides. The remaining heavy metal-poor ashes could be used, for example, as cement additives. In the proposed process of our study we used bypass dust from the cement industry as chloride additives to the bottom ashes. We aim to determine experimentally the optimal conditions to remove heavy metals from ashes and to simulate this process by thermo- chemical modeling. In our experiment we investigate heavy metal flows by heating of differently composed mixtures of bottoms ash and bypass dust in dependence of different furnace temperatures (500-1200 °C). Furthermore, we investigate the reactivity (leaching characteristic) of the resulting product in order to predict if secondary residues can be landfilled in agreement to Swiss regulations for inert materials.IntroductionThe incineration of garbage is generally considered as the most environmentally friendly method for the reduction of municipal solid waste. This is because, compared to traditional storage of waste on landfills, incineration produces less greenhouse gases and destroys toxic organic compounds. The released exothermic energy can be recuperated and the residues from the combustion chamber (bottom ash) are strongly reduced in volume. However, they still form about 600 kt of waste per year in Switzerland, which needs to be landfilled. However, these residues could be potentially used as construction materials after mechanically recovering ferrous and non-ferrous metals. However, the resulting ashes (discharged dry or wet) still contain increased amount of heavy metals (exceeding state regulation) requiring them to be finally deposed on a hazardous waste site. A thermal treatment of these ashes could enable both, to separate and recuperate the remaining heavy metals and an inorganic heavy-metal poor material. The evaporation of metals depends on temperature and can be lowered by addition of chlorides, which would lower the boiling point of most metals by formation of metal chlorides (table 1). 745"

Jan 1, 2008

By Akram Alfantzai, Farzad Mohammadi, Maysam Mohammadi

"Degradation of lead anodes has always been a major concern among the electrowinning industries. In this study, the effect of agitation of the zinc electrowinning solution on the integrity of lead anodes was investigated. Galvanostatic experiments were performed at 37±0.5°C using 0,600 and l000rpm magnetic stirring rates for 24 hours. The Pb02 layer formed on the anode surface was reduced to PbS04 (discharged). The discharge information was used to calculate the amount of Pb02 present on the surface. Weight loss measurements along with the discharge calculations revealed that the degradation rate of the lead anode increased as the solution was stirred more vigorously. Furthermore, the amount of remaining Pb02 on the surfaces was decreased as a function of solution velocity. Therefore, it may be concluded that, degradation rate oflead anodes is controlled by detachment of the corrosion products from the surface rather than by electrochemical reactions. IntroductionElectrowinning is one of the extraction stages of zinc, in which pure zinc is deposited from acidic solution after froth flotation, roasting and leaching processes. The anode electrode materials play important roles in the electrowinning process. Their electrocatalytical capacities determine the oxygen evolution overpotential, and consequently the cell potential and energy efficiency of the zinc electrodeposition [l]. Purity of the zinc deposited on the cathode is affected by the solubility and corrosion resistance of the anode materials. Using insoluble materials as anode in the electrowinning leads to the higher purity of the deposited metal on the cathode[2]. Lead (Pb) and its alloys have been used as the anode in the zinc electrowinning because of its special properties such as relatively low cost, low melting point, insolubility in solutions containing sulphuric acid and high conductivity in both states of metallic and oxidized [3, 4]. In zinc electrowinnig, zinc reduction occurs on the cathode (reaction 1) and the oxygen evolution reaction (OER) (reaction 2) is the main anodic reaction [5, 6]."

Jan 1, 2013

By Christian Ludwig, Virginie Silberstein, Rizlan Bernier-Latmani, Simona Regenspurg

"Residues from waste incineration (bottom ashes) form large amounts of heavy metal-rich waste. Theoretically, heating and the addition of chloride to the ashes could remove these metals by formation of volatile metal chlorides. The remaining heavy metal-poor ashes could be used, for example, as cement additives. In the proposed process of our study we used bypass dust from the cement industry as chloride additives to the bottom ashes. We aim to determine experimentally the optimal conditions to remove heavy metals from ashes and to simulate this process by thermo- chemical modeling. In our experiment we investigate heavy metal flows by heating of differently composed mixtures of bottoms ash and bypass dust in dependence of different furnace temperatures (500-1200 °C). Furthermore, we investigate the reactivity (leaching characteristic) of the resulting product in order to predict if secondary residues can be landfilled in agreement to Swiss regulations for inert materials.IntroductionThe incineration of garbage is generally considered as the most environmentally friendly method for the reduction of municipal solid waste. This is because, compared to traditional storage of waste on landfills, incineration produces less greenhouse gases and destroys toxic organic compounds. The released exothermic energy can be recuperated and the residues from the combustion chamber (bottom ash) are strongly reduced in volume. However, they still form about 600 kt of waste per year in Switzerland, which needs to be landfilled. However, these residues could be potentially used as construction materials after mechanically recovering ferrous and non-ferrous metals. However, the resulting ashes (discharged dry or wet) still contain increased amount of heavy metals (exceeding state regulation) requiring them to be finally deposed on a hazardous waste site. A thermal treatment of these ashes could enable both, to separate and recuperate the remaining heavy metals and an inorganic heavy-metal poor material. The evaporation of metals depends on temperature and can be lowered by addition of chlorides, which would lower the boiling point of most metals by formation of metal chlorides (table 1)."

Jan 1, 2008

By Zenjiro Asaki

The copper concentrate particles dissolve quickly into the molten matte in the smelting furnace of Mitsubishi Process, which indicates that the sulfide smelting is essentially a gas/liquid reaction. In this paper, theoretical calculation has been made on the rate of oxidation of FeS component in the matte to form FeO by rising gas bubbles using the penetration theory. The results showed that all the oxygen in the bubble of 1.2 cm in diameter, which is the maximum stable diameter, is consumed in 3 ms. This time required is sufficiently short, and it results in the actual operation of smelting furnace of 1100% oxygen-efficiency. These calculations indicate that most smelting reactions are completed just under the lance, except slag formation.

Jan 1, 2002

By J. W. Perez

In the treatment of process effluents containing metal ions, it is sometimes desired to remove all of the heave metal ions while at other time it is, desired to remove one heavy metal ion from another, selectively. Ion and precipitate flotation processes were evaluated to perform these functions using the copper-iron aqueous system as a model. Because preliminary foam fractionation experiments proved to be relatively inefficient, most of this work has focused on precipitate flotation using both hydroxide and sulfide precipitation. Test results indicate that by proper control of reagents and operating conditions, it is possible to substantially reduce the froth volume over that achieved with foam fractionation and to separate copper from iron selectively. Mechanisms for collector attachment to precipitates were studied.

Jan 1, 1992

By P. G. Schirk, D. J. Roth

ALTEK has developed a processing system that can receive large pieces of dross & bath, of various metal contents, and reduce and separate these highly metallic concentrates into oxides and non-metallics. This system achieves these results without grinding the metallics into fines. Its unique feature results in the preservation of metallic unit in its largest possible size, which allows for maximum .metal recoveries. The Tumbler, an ALTEK-Didion International joint development, and the ALTEK High Velocity Impacting System (HVIS) are the key elements to this process. This paper will explore the advantage of this cold cleaning system over the direct melting of the raw dross in the reduction of landfill waste. The system also works well for removal of the aluminum from bath from primary smelters.

Jan 1, 2000

By M. Dattilo

Research has been conducted over the past three years using the composite anodes versus the lead alloy anodes. The Merrlin composite anodes have shown the improved performance in copper electrowinning versus the lead-calcium-tin anodes. Using the composite anodes a 100-150 mV reduction in anode overpotential has been observed versus the lead alloy anodes in sulfuric acid electrolyte. The composite coating has excellent corrosion inhibiting properties, and reduces or eliminates the formation of manganese oxide scale. Laboratory evidences indicate that, the use of these composite anodes enhances the process of electrowinning by improving the lead alloy corrosion resistance, lowers the electrode potential, reduces the need for cobalt addition, eliminates the anode cleaning, and reduces the generation of acid mist. Field tests are underway.

Jan 1, 1999

By Takahiko Okura

Sulphur, with its multiple oxidation states, play critical roles in many processes, ranging from regulating enzymes in plants, to acidifying aquatic systems, and to affecting the global climate. Most of non-ferrous smelters have been contributing to reduce atmospheric emissions of sulfur dioxide to acceptable levels, converting it to sulphuric acid and/or gypsum. However, some amount of SO2 gas is still emitted from isolated smelters. Furthermore, sulphuric acid is competing with involuntary elemental sulphur in the market. This situation puts the non-ferrous metallurgical industries to develop a new sulphur fixation process. This paper briefly describes the new technologies for fixation, followed by the novel proposal to convert SO2 gas to elemental sulphur using organic materials. Finally, the feasibility will be presented technologically and economically.

Jan 1, 2006

By Tang Chaobo

Employing manganese carbonate ore and zinc oxide dust as material, Mn-Zn compound oxide powder for soft magnetic ferrite was prepared by a serial methods, as follows: leaching by using sulfuric acid, removing aluminium and silicon by neutralization and flocculation method, using ammonium bicarbonate to co-precipitating Mn and Zn, calcinations and washing to removing impurity content. The optimal technical condition was obtained by experiments. The difficulty of removing impurity such as Si, Al, Ca, Mg, from leaching solution was solved. The impurity content in the production meets with the preparation standard of high quality soft magnetic ferrite. The compound oxide powder obtained in the experiment was made into lower power loss magnetic ferrite, the quality of magnetic ferrite meet the standard of PC40 which was established by TDK corporation.

Jan 1, 2006

By W. F. Drinkard

Many in the environmental movement have focused on this element. But, nothing they or anyone does will change the amount of arsenic in the world. This report is on actual commercial plants that we developed and operated to recover or stabilize arsenic values from metallurgical dusts from gold and copper pyro operations and arsenical gold bearing ores. When they were available gold and copper values were recovered. Our experience in arsenic extends over thirty years. My first corporation, Mineral Research & Development Corporation was the first in North America to manufacture the then new CCA (copper-chrome-arsenic) wood preservatives. This class of wood preservatives proved to be so effective that it made wood into an entirely new material of construction. It is not uncommon for wood properly treated with arsenical CCA preservatives to last for thirty; forty, and sixty years. Over a hundred years have been projected in some field tests. Hundreds of thousands of trees have been saved. Millions more trees would have been saved had environmentalists not decided that their arsenic phobia was more important than trees. There are several variations of CCA. The most popular is CCA-C. Its formula is: CrO3 . . . . . . . . . . . . . . . . . . . 47.5% CuO . . . . . . . . . . . . . . . . . . . 18.5% As2O5 . . . . . . . . . . . . . . . . . 34.0% Until recent restrictions were placed on the consumption of arsenical wood preservatives, annual consumption in North America was about 150,000,000 lbs./yr. About 64,500,000 of arsenic as the pentoxide was safely consumed this way. World CCA consumption has been about double the above figures or 300,000,000 lbs. as 100% CCA and 129,000,000 lbs/yr as As2O5. Close to 100% of all the arsenic used in wood preservatives is derived from gold or copper processing. The valence of arsenic required for CCA wood preservatives and many other markets is the same valence that is required for stabilization. The economic challenge is how to get there. We have built and operated eleven plants to oxidize arsenic trioxide to its pentavalent form. Most of these have been classic in that they used a common oxidants such as hydrogen peroxide or nitric acid to achieve this.

Jan 1, 2005

By Yong Hwan, Wang Jian-Jun, Cai Jiu-Ju, Chen Chun-Xia

"The quantity of residual-heat and its recovery in some Chinese sinter plants are investigated. The main factors affecting energy consumption are analyzed using exergy analysis combining energy level analysis. It is indicated that the “gradation recovery and cascade utilize” of discharged gas and sinter residual heat in different temperature is the direction and the available approach to reduce energy consumption of the sinter process. Taking an iron& steel enterprise as an example, the three-ranked scheme of residual-heat recovery is put forward: ?Part of the sinter gas is used for warm-up and dryness; ?The high-temperature part of the cooler and exhaust-heat boiler are actualized as a closed-circuit, which can produce high-quality steam to generate electricity. ?The waste air in low-temperature part is introduced to sintering machine to support combustion. According to the CDQ which can recover the coal heat, the assumption of pot-recovery is put forward to replace the belt cooler. The two equipments of residual-heat recovery are analyzed in the aspect of energy consumption and CO2 reduction.1. IntroductionEnergy consumption in sintering is only inferior to iron-making in iron& steel enterprises, accounting for 10%~20% of the total energy consumption. A lot of residual heat is produced during sintering, and mostly from the sinter ore and waste gas. Sensible heat of hot sinter ore and discharged gas have accounted for 60%[1] (equals to 40 kgce/t-ore), which are the key point of sintering waste heat recovery. Discharge gas of sintering is mostly composed of flue gas deriving from sinter bed’s combustion, and the content distribution of H2O and O2 and the temperature of the gas along the length of belt-type sintering are shown in Figure1[2,3]. Currently, the sensible heat of hot sinter ore is mainly recovered by circular cooler and cooled by blasting air: the temperature of cooled discharge gas brings down from 350? to about 100? along with the decrease of sinter ore temperature. It is significant to recovery and reuse the waste heat as 4000~6000m3 discharge gas per ton of ore can be produced"

Jan 1, 2008

By Shuo Wang, Yu Wang, Bing Xie, Rui Tang, Hong-Yi Li, Kun Wen

"During present converter vanadium extraction process, phosphorus could not be removed from hot metal due to absence of CaO in slag though it is an efficient way for vanadium extraction. In order to improve the phosphorus remove and produce CaO-containing vanadium slag, which could be directly used in subsequent roasting process, during the converter vanadium extraction process, lime dissolution in FeOx-Si02-V203-Ti02 slag was investigated by using a rotating cylinder technique and the slag-lime interface was characterized by SEM/EDS. Results showed that changes in the slag chemistry and phase compositions during the lime dissolution process were similar to that in CaO-Si02-FeOx based slag during the BOF process. The V and Ti in the slag were expected to diffuse into the lattice of2CaO·Si02 solid solution, which formed a rather thinner layer in thickness at the slag-lime interface than that in BOF process, leading to improvement of lime dissolution in the slag.IntroductionVanadium is important material that widely applied in industries. The traditional technique to extract vanadium was to leach vanadium after sodium salt roasting. However, the sodium salt roasting process has several problems including lower yielding rate[!] and environmental pollution[2]. Therefore, the more environment-friendly technique of calcium roasting[3-4] was proposed. In order to increase roasting efficiency of vanadium slag, it is essential to study the dissolution/reaction mechanism between lime and vanadium slag. Many investigations about the dissolution reaction of lime in molten slag have been carried out from the standpoints of rapid slagging to De-Pin steelmaking process[5-6]. However, their studies were focused on BOF slag and the reaction mechanism between solid lime and slag containing vanadium has not been reported yet. In present work, the dissolution process was studied with rotating cylinder technique and the reaction interfaces were observed and analyzed by SEM/EDS to elucidate the dissolution mechanism of lime in vanadium slag. This work was supported by National Natural Science Foundation of China No. 51090382."

Jan 1, 2013

By Mingming Zhang

"Three samples received from the EAF shop have been characterized by chemical, X-ray diffraction (XRD), optical microscopy (OM) and scanning electron microscopy (SEM) methods. The objective of this characterization work is to investigate the occurrence of nickel, copper, zinc, sulfur and phosphorus in these samples and identity their origin and associations with iron minerals in the concentrate samples that are from mines.The samples were identified as Mineral, Pellet, and HRD. The latter is the DR! product. All three samples were received as fine powders. The results indicate that, in the mineral sample, magnetite is the major iron oxide mineral with hematite as a second phase based on the OM and XRD studies. Pyrite [FeS2], chalcopyrite [CuFeS2] and bravoite [(Fe,Ni)S2] are major sulfide minerals. Trace amounts of apatite [Ca5(P04)3(F,Cl,OH)], wardite [Na4CaA112(P04)8(OH)8 6H20], giniite [Fe5(P04)4(OH)3 2H20] and vivianite [Fe3(p04)2 8H20] were identified by SEM and XRD. Microscopic studies also indicated that most of the sulfide grains in the mineral sample are present either as liberated fine particles (about 10 microns) or as inclusions within the magnetite and hematite grains. XRD studies revealed magnetite as the major mineral with subordinate amounts of hematite and pyrite confirming the microscopic findings. Copper, nickel, and zinc are mainly present as chalcopyrite, bravoite, and franklinite [(Zn,Mn,Fe)(Fe,Mn)204] in trace amount in the mineral samples, respectively. Impurities carry over to the Pellet and HRD samples.Chemical analyses of the three iron-bearing samples indicate that sulfur and phosphorus in the Pellet sample exceeded the specification. Since liberated pyrite and chalcopyrite particles were observed both in mineral and pellet samples, magnetic and flotation processing routes for this ore should be effective for sulfide removal but at the cost of iron losses. The high phosphorus content of all three samples indicates that there are phosphates which are difficult to remove by the current concentrating process (magnetic separation and flotation)"

Jan 1, 2012

By M. Fafard, R. Ahmed, O. Dion-Martin

"The optimization of aluminum sheet and tube forming needs the use of large strain finite elements software. The precision of the predicted results from those simulations depends mainly on the quality of constitutive law of the material used. In order to improve quality of these simulations, Barlat has suggested a new yield function named YLD2000-2d. This criterion describes the anisotropic behavior of the rolled aluminum plates. This work consists of characterizing the AA5754 alloy and estimating the material parameters needed for the YLD2000-2d criterion in LS-DYNA. In order to get these parameters, various mechanical testing were performed such as bulge and tensile tests. Moreover, the bulge test was also used to obtain an estimation of work hardening curve in large strain condition, up to 50%. The objective of this paper is to share the experimental results of the characterization of AA5754 aluminum alloy.IntroductionResearchers from National Research Council Canada's Aluminium Technology Center (NRCATC) and Aluminium Research Centre - REGAL, are working on aluminium tube hydroforming processes of AA-5754-0 alloy, used in automotive industries. Hydroforming process presents several difficulties such as wall thinning and section changes. In order to control them, some parameters can be set during the process like pressure rate and end feed level [1]. Given the complexity of the parts and the variability of the control parameters, the use of finite element method (FEA), like LS-DYNA, based on large strain theory is thus necessary. The accuracy of predicted results depends mainly on the quality of the constitutive law used to model the behavior of material. FEA results seem to be valid with the von Mises yield criterion used in some cases. But, given the anisotropic properties of the AA-5754 alloy, a more appropriate criterion could be used. The *MAT_ BARLAT YLD2000 shell material criterion, developed by Barlat [2], who's taking into account the anisotropic behaviour, was chosen due to its large flexibility and its good adaptation to particular elastoplastic behavior of aluminum. However, the use of this criterion needs to determine some material parameters by experimental way."

Jan 1, 2013

By Grant Wallace, Rod James, Larry Twidwell, Ed Rosenberg, Courtney Young, Sean Dudley, Hsing-Hsin Huang, William Gleason, Jerome Downey

The use of applied chemistry in the production and optimization of leach solutions from Rare Earth Element (REE) ores and concentrates is being investigated. Ore and concentrate samples were characterized using scanning electron microscopy/mineral liberation analysis (SEM/MLA), X-ray diffraction (XRD), and Atomic emission inductively-coupled plasma spectroscopy (ICPAES). Multiple leach tests were performed to analyze the effects of temperature, residence time, and reagent concentration on the leaching of REEs. Analysis of leach solutions was carried out using ICP-AES. Modeling and statistical analysis of extraction behavior was carried out using DesignExpert 9. Modeling data for cerium extraction indicates that extraction is greatly influenced by temperature and reagent concentration, while leaching time plays a much less important role. Experimental design techniques are being utilized to optimize REE recovery. Results, conclusions, and directions for future studies will also be discussed.

Jan 1, 2015