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By H. Y. Sohn

The purpose of this article is to analyze critically and quantitatively the effect of chemical equilibrium on the overall rates of fluid-solid reactions. It is shown through a mathematical analysis that a reaction with a small equilibrium constant (a positive standard free energy of reaction) is more likely to be rate-controlled by pore diffusion or mass transfer than a reaction with a large equilibrium constant. The overall reaction rate of the former also tends to be slow. Furthermore, the apparent activation energy of such a reaction approaches the standard enthalpy of reaction (Mf'), rather than the true activation energy of the chemical reaction. The Law of Additive Reaction Times developed by the author is shown to apply to equilibrium-limited fluid-solid reactions and to be useful in quantitatively analyzing the behavior of such reactions.

Jan 1, 2003

By Reinhold G. Schulze

Thiourea is being applied as an industrial leaching agent for gold and silver only in a few cases. A GIP technique was developed which eliminates most of the obstacles against its use. Omission of an acid treatment and mild conditions for precious metals stripping from the loaded carbon simplifies process conditions in comparison to cyanide CIP technique. Examples are given.

Jan 1, 1989

By A. R. Udupa

The reduction roasting behavior of chalcopyrite has been investigated using various combinations of a desulfurizing agent, i.e., CaO or Na2CO3, and a reductant, i.e., CO, H2 or C. Using these, combinations the sulfur is removed from the mineral as CaS or Na2S rather than SO2 as is the case with conventional copper smelting and converting. The laboratory reduction ex¬periments were conducted using thermogravimetric analysis (TGA) and boat tests of mixed combinations of fine particulate reactants subjected to a continuous gas stream. The degrees of metallization were determined by both weight loss and chemical analysis methods and the products examined using optical and scanning electron microscopy and electron probe microanalysis. The percent reduction after one hour at 900°C ranged from 60% to 94%. From these data It was possible to provide postulations as to the controlling reduction mechanisms.

Jan 1, 1983

By Chang Wei, Zhigan Deng, Jiqiang Liao, Minting Li, Hongsheng Xu, Yan Song, Cunxiong Li, Xingbin Li

"Abstract: Direct ?otation of oxidized zinc-lead ore is characterized by recovery of zinc and lead only around 55% and 50%, respectively. Mineralogical analysis shows that the sample used in the present study is a carbonate hosted zinc-lead ore, with a zinc and lead carbonate content that accounts for 80.14% and 75.63% of the total minerals, respectively. The carbonate hosted zinc-lead ore was hydrothermally sulfidized with elemental sufur and the experimental data indicated that under the conditions employed up to 75% zinc and 82% lead sulfidation extent were achieved. As a result of pre-sulfidation followed by flotation, the recoveries of zinc and lead into flotation concentrate were over 90%. A flotation concentrate was obtained with 52% Zn and 37% Pb from the materials which was treated by sulfidation.IntroductionSulfide ores are the primary source of zinc and lead, and they are becoming depleted; thus, metallurgical investigators are interested in using abundant oxidized zinc-lead ore reserves. The high-grade zinc-lead oxidized ore, which normally has a zinc content higher than 15%, can be disposed of by acid leaching and electrolysis. However, the low-grade ore, which has a zinc content lower than 10%, is difficult to smelt with pyrometallurgy and hydrometallurgy, and the processes are very complicated and expensive in terms of production flow and energy consumption. Therefore, making the low-grade oxidized zinc-lead ore more beneficial has become more important in recent years. Flotation is the most common process, and the primary method of recovering zinc and lead from sulfide or oxide minerals. It is well known that there is a difference between sulfurized and oxidized minerals regarding their separation by flotation. Flotation of zinc and lead oxidized minerals is extremely complex because of the similarities in the physicochemical and surface chemistry of the constituent minerals. There are no known direct-acting collectors capable of producing single metal concentrates [1-3]."

Jan 1, 2012

By Yanjie Liang

Elemental sulfur and volatilization kiln slag(VKS)containing heavy-metal produced by smelter factories were used to produce sulfured building material. The effects of heating mode, material proportion (MSulfur:MVKS), size of waste particles and ratio of aggregate to filler(A/F) on the mechanical properties and leaching toxicities of solidified stuff were investigated. The optimal conditions for the solidification are stepped heating mode, 3:7 ratio of MSulfur to MVKS, particle size less than 150µm and 3/17 ratio of A/F. Under the above optimal conditions, the compressive strength of solidified stuff rises to 35 MPa, and water absorption is down to 4%-6%.Furthermore, when NaOH is applied as an additive in the process of solidification, the 2+concentrations of most heavy metals except Pb have reached the national leaching toxicity standard. The results of X-ray diffraction reveal that sulfured solidification is caused by the physical encapsulation rather than chemical transformation.

Jan 1, 2010

By Benjamin P. Hay

Complexation of a metal ion to a ligand often results in structural changes that introduce steric strain within the ligand. A design criterior:1 for ligands that will complex metal ions more strongly is to choose Iigar:1d architecture, that minimizes this strain. This paper describes how molecular mechanics models can be used to define the degree of ligand binding site organization in terms of' ,strain energies associated with conformational reorganization and distortion of the binding conformer. This approach yields a method to predict how modifications to ligand structure will affect metal binding affinity.

Jan 1, 1999

By Alan P. Prosser

The heap leaching of gold ores by cyanide solution was simulated by computer program. The program uses only basic m1neralogical and chemical data; no process testwork data, such as column leach results, are required. The simulation can be used to forecast the consequences of various changes before and during the testwork, design and operation stages of a particular ore-process system. Also, data about the state of different parts of the heap at various times help create an understanding of what is happening. The effects of mineralogical and process variables on the overall performance of the ?heap leaching process are illustrated. Comparisons are made to column leach tests and production data. The potential of the simulation strategy is discussed for making better use of operating experience and for suggesting specific research objectives. It has become clear that more attention should be paid to other metals that dissolve in the solution.

Jan 1, 1989

By F. Michael Hosking

Modeling of a furnace brazing process is described. The computational tools predict the thermal response of loaded hardware in a hydrogen brazing furnace to programmed furnace profiles. Experiments were conducted to validate the model and resolve computational uncertainties. The results from selected furnace simulations and measured thermal events were compared. Critical boundary conditions that affect materials and processing response to the furnace environment were determined. "Global" and local issues (i.e., at the furnace/hardware and joint levels, respectively) are discussed. The ability to accurately simulate and control furnace conditions is examined.

Jan 1, 1998

The generation of acid mine water is? due to the oxidation and weathering of sulfide bearing tailings and overburdens. Ferrite precipitation prooess has been applied to treat acid mine water. The conventional ferrite preC1pitatlon requires air oxidation at high temperature, or long aging time or addition of magnetite powder ,as promoter. In this investigation, a modified ferrite, precipitation process is developed by which magnetic ferrite can be produced at an ambient temperature. Acid mine waters from Berkeley Pit (Montana, U. S. A.) and from Noranda Tailings (Quebec, Canada) were used. The co precipitation of heavy metals from these two acid mine waters is studied as a function of FeIM molar ratio, oxidation time and settling rate under applied magnetic field. The investigation indicates that the modified ferrite co precipitation can remove substantially all of the, dissolved metal ions from acid mine water. The ferrite product obtained after precipitation' is characterized by XRD, SEM, BET and saturation magnetization. The results show that spinel ferrite, precipitation can be achieved at room temperature and the saturation magnetization of ferrite product from,acid mine water is comparable to that of pure ferrites.

Jan 1, 1995

By Liping Li

A comprehensive three-dimensional two-phase mathematical model was developed to represent a channel type reactor with intense bottom gas agitation. Tracer dispersion and particle tracing methods were used to conduct the analysis based on the solution of the Navier-Stokes equations. Different operational parameters, such is gas volume flow rate. bubbler separation aspect ratios and liquid Input flow rates, were investigated for the purpose of reactor optimization. The numerical calculations were compared with experimental results obtained at the University of Missouri and a good general agreement was observed. Relatively low longitudinal mixing was observed characterizing the system as a "plug-flow" type reactor, in contrast to the intense vertical mixing, under the conditions investigated. Some general mixing characteristics are also discussed In connection to the behavior of other metallurgical reactors.

Jan 1, 1996

By T. J. A. Smith

This paper provides an overview of some of the key issues in design of smelter gas handling systems, with particular reference to sulphide smelting plants. In both primary smelting and converting. gas handling and treatment systems often represent the major capital cost component. There is also ample evidence that poor system design can be a major cause of smelter down time, lost production and unforeseen high maintenance costs. The paper discusses these issues and offers guidance for improved design.

Jan 1, 1992

By G. P. Swayn

Recycling of dusts produced in a flash furnace by direct injection provides the opportunity to reduce recycle loads to the reaction shaft, lower fuel requirements and possibly increase metal recovery to products. Ausmelt has provided an Ausmelt lance system for injecting dusts collected from the waste heat boiler and electrostatic precipitator units, directly into the slag melt. This has been installed and operated in the Kalgoorlie Nickel Smelter with systems for feeding dust, for firing with oil and air, and for raising and lowering the lance. Modelling and testwork development of dust injection, results of commercial trials and design considerations for further opportunities of the Ausmelt lance system, are discussed.

Jan 1, 1994

By H. Forrest

Lead smelting at Cookson Industrial Materials was formerly carried out using a combination of Blast and Reverberatory Furnaces. In the late 70' s these furnaces were replaced by two 20 tonne capacity Rotary Furnaces. This furnace type has proved to be more flexible in the range of feedstock that can be processed, including lead drosses, battery plate and even whole batteries. High rates of production have been achieved whilst attaining a good level of environmental control. The majority of the sulphur in the feedstock can be fixed by use of appropriate fluxes.

Jan 1, 1990

By Christina V. White

An experimental study was undertaken to investigate the feasibility of utilizing vapor transport for the treatment of heavy metal contaminated smelter soils. The focus of this project was to develop process chemistries that would make incineration a viable process for the treatment these soils. The experimentation concentrated on the elimination of arsenic, cadmium, and lead, and was performed in a laboramry scale rotary kiln setup. Three soil samples from non¬ferrous smelter sites, which contained various concentrations of contaminants, were utilized in the experimentation. Three chemistries were investigated for the volatilization of the heavy metals: Chloridizing volatilization, ferric chloride vapor complex formation, and the use of oxygen potential control. The samples were analyzed for residual heavy metals so that the extractions could be determined. However, the ultimate test was the leachability of the residual arsenic, cadmium, and lead, as determined by the TCLP test. The results firmly establish that incineration is a feasible process for the treatment of metal contaminated soils. It was found that no one process chemistry is suitable for all different soil samples. A two-step process consisting of a reducing step followed by a hydro-chlorination step was required to make Soil Sample-B pass the TCLP tests for all three heavy metals. Soil Sample-A passed the TCLP tests for arsenic, cadmium, and lead using a hydro-chlorination process at a minimum temperature of 700°C. In addition to passing the TCLP mm for Soil Sample-A and Soil Sample-B, 70 to 80 percent removal of the impurities was accomplished. This demonstrates that the leachability of the impurities was decreased primarily due to the removal of a large fraction of the contaminants, Soil Sample-C possessed very high levels of cadmium and lead and only moderate extractions of the impurities were generated from this soil. The arsenic TCLP test was passed at 500'C using a process gas containing ferric chloride and at temperatures of 700°C and above using chlorination of hydro-chlorination.

Jan 1, 1996

By Michael L. Free

Bacterial oxidation of an arsenopyritic gold-ore .concentrate was carried out with continuous-flow .operation in 14-liter, mechanically agitated reactors. Samples from the slurry reactors were separated into solid and liquid fractions and analyzed separately to determine the electrochemical rates of sulfide conversion by the bacteria and the rates of direct bacterial oxidation of sulfide. The rates of the individual mechanisms are compared to the overall rates of biooxidation in the continuous-flow slurry reactors. The results show that the commonly hypothesize4 direct and indirect mechanisms of biooxidation both play a significant role in the bacterial oxidation of sulfide ores.

Jan 1, 1991

Thermodynamics and kinetics? of the removal of Va elements (As,Sb,Bi) from copper were investigated 1n the fire relining by alkaline carbonate fluxes such as Li 2co3 , Na 2CO3 and K2CO3. The distribution coefficients of As, Sb and Bl between alkaline carbonate fluxes and mo) ten copper were ?obtained at 1200°C under the different oxygen potentials. As and Sb were easily removed from copper to fluxes as pentavalent oxide form. On the other hand, Bi was hardly removed except by a Ll2CO3 flux. The removal rates of Va elements from copper were also measured In the temperature range of 1150°C.- 1250°C. The removal rates of As and Sb were much higher than that of Bi. The removal rates of Va elements showed the same order of the distribution coefficients. The removal rate could be expressed by following equation. (1).

Jan 1, 1987

By J. M. Rapkoch

In late October 1996, an acid plant at a major U.S. copper smelter was faced with unexpected and rapidly increasing pressure drop across the gas cooling tower in the acid plant, indicating a build-up on the packing. This threatened to halt operations if not resolved. Earlier that month, a smaller vessel in the acid plant was found to be completely plugged with lead sulfate. It was feared that a similar fate awaited the gas cooling tower unless the scale build-up was stopped. Although lead sulfate is present in most copper smelter acid plants, this accumulation was unusually severe. An investigation was launched to find the source of the lead, determine how lead is transported to the gas cooling tower, recommend operating practices to prevent such severe scaling, and seek ways to recycle the lead value in the scale covered polypropylene packing. Late in the investigation it was learned that the lead originated from an improperly executed recycling program.

Jan 1, 2000

By Kenneth L. Driggs

The Environmental Protection Agency's Clean Air Act of .1970 provided the driving force for the current Magma Smelter configuration. The historical and technical perspectives of those process developments are reviewed. Innovations in procedures and equipment have allowed compliance with the requirements of the regulating authorities. The wet scrubbing of converter gasses and the monitoring of converter operations by a controlling foreman are two of the major contributors to these successes. The Clean Air Act Amendments of 1990 have posed many new concerns for all U.S. industry, including the few (seven) primary copper smelters remaining. Future concerns include tightening the sulfur dioxide ambient standard from the current three-hour averaging period to one hour"

Jan 1, 1992

By Edilson Marques Magalhães, Danielly Da Silva Quaresma, José Antônio da Silva Souza, João Nazareno Nonato Quaresma, Emanuel Negrão Macêdo

"The production of alumina from bauxite using the Bayer process generates the residue known by red mud. This material can be used as a source for concentration and recovery of valuable metals such as titanium. The greatest difficulty of concentrating titanium compounds is the large amount of iron oxide present in red mud > 30% by weight. This paper shows the extraction of the iron oxide, increasing the concentration of the titanium compounds. The red mud is leached with H2SO4 at 30% concentration and temperature range of 60°C, 80°C and 90°C. Analysis of the leached and concentrated was made to verify the effectiveness of the iron oxide extracting process and the titanium compounds concentration viability.2- IntroductionIn the state of Para is located the Industrial Unit Alumina of North of the Brazil S/A (Alunorte), created to produce and commercialize alumina, aluminum oxide, Al2O3. The ALUNORTE with Aluminum Brasileiro S/A (Albras) and Mining Rio do Norte S/A (MRN) complete the production cycle of aluminum in the state. Although the production of alumina has a importance great for the socio-economic status, as in any area other, generates a amount large of waste, thus causing environmental impacts. Pará State has produced 25 million tons of bauxite (Pinto, 2010), of which 60% were transformed into alumina plant in Pará and Maranhão by ALUNORTE by ALCOA, generating approximately 9,000,000 tons of waste known as Red Mud (RM). Due to the high reactivity this material is considered dangerous, and currently there is no operating process capable of reuse all the material produced at any refinery. The search for industrial processes in order to reuse these wastes can contribute to reducing the overall impact of the production process of alumina. In this context, this paper estudied, within the research line of Solid Waste valorization the mining industry and metallurgy, a process that makes possible the red mud as a source of raw material, in other words, seeks to maximize the use of red mud as raw material for concentration and or recovery of titanium compounds in both the crystalline form of anatase, rutile and ilmenite, avoiding the predatory extraction of natural resources of these materials. Applying definitely the concept of self-sustainability of the mining industry and metallurgy."

Jan 1, 2012

By Tabbetha A. Dobbins

We report studies concerning the time frame for catalytic reactions between NaAlH4 (sodium alanate) and TiCl3 during high energy milling. Spectral features in x-ray absorption spectra were analyzed for samples milled for various times (0 minutes, 1 minute, 5 minutes, 25 minutes, and 125 minutes). A structural transition from Ti3+ to Ti0 is observed within the first 5 minutes of milling. The Ti0 structure persists for samples milled for times longer than 5 minutes?even after those samples underwent a subsequent single hydrogen desorption/absorption cycle. Samples milled for less than 5 minutes retain Ti3+. For samples milled for 1 minute, the Ti-K edge position shifts from Ti3+ to Ti0 after a single desorption/absorption cycle. However, the first coordination sphere around the Ti0 absorber occurs at longer distances for 1 minute milled sample. These results hint at the formation of Ti0 pure metallic clusters upon desorption/adsorption cycling of 1 minute milled sample. Previously reported x-ray absorption spectroscopy studies have demonstrated the structural transition from Ti3+ (in TiCl3) to Ti0(determined to be TiAl3 found at the surface of the alanate powder). Aluminum deficiency on the NaAlH4 lattice is responsible for controlling hydrogen absorption capacity. These time-resolved spectroscopy studies suggest the possibility for controlling aluminum deficiency, while still maintaining titanium activation of the alanate powder, by manipulating the coordination environment of the titanium dopant during the first five minutes of high energy milling. Specifically, a possible approach to mitigating aluminum deficiency during doping would be to introduce an alternative species to which the to Ti3+ catalyst would form a metallic bond after the TiCl3 has attached at the surface of the sodium alanate powder and before the Ti3+ forms the TiAl3 intermetallic species.

Jan 1, 2006