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By Hector M. Lizama

A new technology, known as the HydroZinc? process, is described for the recovery of zinc from sulphide ores that includes heap leaching, neutralization, solvent extraction and electrowinning. Unit operations were scaled up from bench-scale to a 1-t/d zinc cathode demonstration plant. Bench-scale studies defined the process chemistry and a process flowsheet. Column tests were used to design full-scale heaps for zinc bioleaching, and mini-pilot equipment was used to design a solvent extraction circuit. The characteristics of the process required development of a bleed circuit for water and impurities. The complete integrated process was tested on a demonstration plant scale for two years, with about 10 000 t of zinc sulphide ore being bioleached in two 6-m-tall test heaps. In addition to 1 t/d of zinc cathode, iron hydroxide and gypsum residues were produced. The process also generated a small effluent bleed. Over the course of the two-year demonstration test, a number of technical hurdles were overcome and several improvements were made. Some of the more significant ones are presented along with process descriptions and experimental and demonstration plant data. Some engineering aspects and economic evaluations of the new process are also discussed.

Jan 1, 2003

By J. E. Dutrizac

The behaviour of the lanthanide elements during the precipitation of sodium and potassium jarosites at 98oC from sulphate media was systematically investigated. The lower atomic weight lanthanide elements (La to Gd) are characterized by the limited solubility of their alkali-lanthanide sulphates, such as NaNd(SO4)2?H2O, which commonly contaminate the jarosite precipitates. Hence, single phase jarosite-type compounds were precipitated only from solutions containing <0.4 g/L of the La to Sm lanthanides. The sulphates of the heavier atomic weight lanthanide elements (Tb to Lu) have significantly higher solubilities such that solutions containing up to 10 g/L of the individual lanthanides could be investigated without the precipitation of alkali-lanthanide sulphate species. Even at the highest lanthanide concentrations, however, none of the jarosite precipitates incorporated more than 0.3 wt% of any of the lanthanide elements. Comparable levels of lanthanide incorporation were noted in both Na-jarosite and K-jarosite. Although the mass of the jarosite precipitate increased with increasing ferric sulphate concentration or with increasing pH, the extent of lanthanide incorporation was not significantly affected. Clearly, the trivalent lanthanide elements do not substitute extensively for trivalent iron in the jarosite structure. This behaviour likely reflects the significantly lower hydrolyzability and larger size of the trivalent lanthanide ions relative to ferric ions.

Jan 1, 2003

By A. P. Paiva

Studies focused on the recovery of precious metals by solvent extraction have recently increased. either to devise suitable solvents or to clarify the involved extraction mechanisms and kinetics. In this work, a comparison of the performance exhibited by triphenylphosphine (TPP), bis-(penty1thio)-ethane (BPTE) and triisobutylphosphine sulfide CI"I&apos;BPS) in the extraction of silver from acidic chloride media is carried out. Extraction and stripping isotherms involving the three extractants are presented together with the results obtained on the selectivity of silver extraction against high contents of iron, copper and lead. Attempts to clarify the mechanism of silver extraction by TIBPS were performed by studying the distribution coefficient dependence on ligand and chloride concentrations. The effect of temperature on extraction and stripping is also considered. The interfacial tension for the system, measured with different concentrations of extractant in the organic phase, is analysed.

Jan 1, 1994

By H. L. Ludtke

Microlaminate composites were fabricated by electron-beam physical vapor deposition. The microlaminates consisted of five layers, each 2 to 4 pm thick, and were composed of either pure metal layers (Cu-Ag), or alternated between metal and intermetallic layers (Nb(Al)- Nb3Al). The microlaminates were heat treated in an Ar atmosphere for 2 to 12 hours, at temperatures of 600°C for the Cu-Ag and 1000°C to 1200°C for the Nb(Al)-NbsAl. Microlaminates were examined after deposition and after heat treatment by scanning electron microscopy and energy dispersive x-ray spectrometry. The effects of heat treatment on the morphological stability of these composites will be described.

Jan 1, 1999

By Spencer Peng, Larry Wasik, Akram Alfantazi, Michael Mahon

A dynamic simulation of a zinc tankhouse is a potential tool to improve tankhouse production and cost efficiencies. A fully dynamic simulation has potential uses in the design of new tankhouses as well as in the optimization of existing facilities. Equations from previously validated models of a single cell have been adapted to the industrial dynamic process simulation software, CADSTM Plus. Based on the inlet concentration, current density, and electrode setup, the simulation can predict many parameters, including outlet concentrations, flow rates, current efficiency and energy consumption. Multiple cells have been simulated simultaneously, allowing for an entire hypothetical tankhouse to be modeled. The simulation can be used to dynamically predict the conditions in a zinc tankhouse throughout an operation time scale. Further applications of this model include, tracking impurity buildup, modeling of recycle streams and the development of new flow regimes within the tankhouse.

Jan 1, 2012

By Mariana H. Staia

Thermodynamic calculations based on the free energy minimization method were performed for the system Ti-Fe-Mn-0-C1-C in order to evaluate the chemistry associated with the chlorination of an ilmenitic concentrate using CCl4. In the calculations various weight ratios of FeTi03/ CC14, a , were considered, which varied between 0.32 to 0.98 at temperatures ranging from 673 K to 1273 K , at atmospheric pressure. The results obtained indicated that the operating conditions for a process in a packed bed reactor, which implies the chlorination of both Fe and Ti, are 0.39 < a < .49 at T 1173 K.

Jan 1, 1993

By Kazuhiro Asai

Nippon Mining and Metals Company has an annual indium production capacity of 30 tons at its Saganoseki smelter and refinery. Lately, indium content in the. zinc smelting dust, one of the main sources, has been on the decrease while the amount of impurity in it on the increase. The present process at Saganoseki does not permit efficient elimination of a large. amount of impurity. Therefore, studies were conducted to improve its recovery process. As a result, a new indium recovery process consisting of leaching, solvent extraction and electrowinning has been developed. The new process was tested at a pilot plant and satisfactory results were obtained. This new process is discussed in this paper.

Jan 1, 1995

By Hiroshi Ono

"By newly developed ICP method, trace amounts of As(III), As(V) .,Sb(III) and Sb(V) were precisely determined within accuracy of sub ng/ml. As(III) and Sb(III) were separated from As(V) and Sb(V) by extracting into ·xylene as diethyldithiocarbamate complexes using diethylammonium diethyldithiocarbamate (DDDC), and then back-extracted into nitric acid for a quantitative determiruition by ICP-AES equipped with hydridegeneration system The recoveries of As(III) and Sb(III) were satisfactory throughout the extraction with 0.04mol/l DDDC in xylene from lmol/l hydrochloric acid solution and the back-extraction with 7 mol/l nitric acid. As(V) and Sb(V) were reduced to As(III) and Sb(III) by ascorbic acid and potassium iodide, and their quantities were determined as mentioned above. The detection limits were found to be 0.58ng/ml for As(III), 0.63ng/ml for Sb(III) using 50ml of a sample. The proposed method was applied to analysis of the real sample.Introduction In drain, arsenic(AS) concentration is prescribed below 0.lmg/l, so As must be removed. As is existed at .the form of As(III) or As(V) in solution. For t1Jeir difference of chemic;µ property, it is not easy to remove As in solution. So it is an urgent necessity to develop for determining concentration of As(III) and As(V). Antimony( Sb) has resemblance .chemical property to As. So Sb was experimented the same as As.The separation and determination of As(III) and As(V) have been carried out using several methods, such as ICP after copreclpitating separation, HPLC, direct hydride generation atomic absorption. However these methods have some problems. One of main problems is that HPLC and direct hydride generation atomic absorption methods are influenced by coexisting elements."

Jan 1, 2000

By Jinxing Ji

The thiosulfate lixiviant system for leaching of gold has been under extensive investigation for nearly two decades and consists of ammonium thiosulfate, copper and ammonia. There are several challenges with this system. The occurrence of ammonia must be taken into account from a health and hygiene aspect in the workplace, and also from an environmental perspective with significant levels of ammonia and copper in the tailings. Copper accelerates the leaching rate but causes excessive thiosulfate degradation. A new lixiviant system that has been investigated consists only of sodium thiosulfate without copper and ammonia. Gold leaching is carried out in an enclosed reactor with slightly elevated oxygen overpressure and temperature. Extensive leaching experiments were carried out to minimize thiosulfate degradation and polythionate formation while maximizing the gold extraction. For the preg-robbing carbonaceous ore sample tested, gold leaching was essentially complete within six hours and the thiosulfate consumption was lower than in the typical ammoniacal thiosulfate system. The gold thiosulfate complex in the pregnant leach solution was found to be quite stable under ambient conditions. This new leaching system has the advantages of being more environmentally friendly, has a shorter residence time, lower thiosulfate consumption, lower oxygen consumption, and is easier to control.

Jan 1, 2003

By Matthew D. Andriese, Jiann-Yang Hwang, Zhiwei Peng

"It has been demonstrated that metallic-bearing minerals are physically liberated from host rock when exposed to microwave (MW) energy. The metallic minerals are iron sulfides and spinel oxide minerals contained in peridotite rock. Experimental evidence has shown ore particles readily couple with MW energy at 2.45 GHz, 1000 W resulting in rapid heating. Thermal stresses are generated by highly absorbing metallic-bearing minerals resulting in cracking and embrittlement of ore particles that assists in crushing and grinding processes. The liberated metallic-bearing minerals are shown to report to coarser size fractions as a result of MW exposure.IntroductionComminution of ore material during beneficiation is a large energy expenditure for the mineral processing industry. Crushing and grinding operations alone consume 50-70% amount of energy used in mineral processing [1]. Size reduction becomes increasingly difficult with decreasing particle size making grinding the most energy-intensive step of comminution. The aim of comminution is to maximize liberation of economically valuable minerals from the host rock [2]. Overall, the less material that needs to be handled, then grinded, to create a useful product for hydro/pyro metallurgical processes will achieve the greatest reduction of energy.Much of the scientific interest for use of microwave (MW) energy in mineral processing has been for improved hydro/pyro metallurgical techniques [3-6]. Early authors have employed MW energy for improved grinding of ore particles but most conclude the energy savings do not justify the energy input [7-9]. The effectiveness of MW assisted grinding is dependent on the ore mineralogy and the absorptive properties of minerals contained within it. Ore containing magnetic minerals should prove successful with MW assisted breakage from highly absorptive properties."

Jan 1, 2012

By T. Langthaler, H. W. Engl, H. Holl, K. L. Schwaha

"The trend towards near net shape casting requires the development of more complex design and control algorithms for continuous casting ""machines in particular with respect to the solidification process.Compared to conventional continuous casting the reduction in casting thickness allows to influence more directly the solidification rate by control variables like surface cooling and/or casting speed.In order to enable the determination of these control variables for a given solidification profile, an algorithm (inverse solidification analysis) has been developed based on nonlinear constrained optimization. The application of the model is illustrated by practical examples ranging from conventional continuous casting to advanced thin slab casting.IntroductionProcess development in the Iron and Steel Industry is directed towards the realization of continuous process sequences. Since the direct linkage of processes imposes some restrictions onto the individual process steps, more complex algorithms are needed for design of equipment and control of operation. In particular the recent trend to reduce casting thickness, i.e. to cast thin slabs, has made the direct coupling of continuous casting and rolling absolutely necessary. The prospective development in strip production is schematically shown in fig. 1."

Jan 1, 1988

By Chang Wei, Zhigan Deng, Yizhao WANG, Cunxiong Li, Gang Fan, Xingbin Li

During the process of hematite precipitation, the transformation of Na jarosite convert into hematite has been studied in a batch reactor at different temperatures, ranging from 170°C to 200°C with 3h of the retention time in the presence of 30g/L Fe ( ) and 4g/L Na+. The composition of precipitation was seriously depended on the temperature, at 170°C hematite and sodium jarosite are the reaction products of iron precipitate, with an increasing in reaction temperature the sodium, sulfur content in precipitated decreased and sulfur mainly exist in forms of SO4 2-, and when temperature over 200°C hematite was the only phase in product. An increasing temperature was not only beneficial to iron precipitation, also conducive to jarosite conversion to form high quality hematite precipitate.

Jan 1, 2016

By F. Kongoli

A computerized thermophysicochemical database is being developed for various processes involved in nickel smelting and converting. This database includes optimized models for slag, matte, liquid and solid alloys in the multicomponent system(s) as applied to batch and continuous nickel smelting and converting processes. This database can be used to quantify the multicomponent and multiphase slag/matte/alloy/gas equilibria, liquidus and solidus surface, tie-lines, solubility and/or losses of nickel and other components in the slag, distribution coefficients, components activities, heat and mass balance, etc. The database also includes optimized models for the viscosity of the slags associated with any of the above processes. Both databases are coupled and this constitutes a very effective method to quantify the effect of each component on several parameters of the smelting and converting processes and to diffuse the confusion that exists in the literature. Several application examples have been given to demonstrate the usefulness of this database for quantitative prediction of the thermophysicochemical properties of the phases involved in actual or developing processes, even in the areas where experiments are difficult or impossible. The considerable cost reduction that results ftom the use of this database as compared to other methods in the improvement of existing technologies or in the development of new ones is discussed along with continuing new developments of this database.

Jan 1, 2002

By Amy Nelson

In the electrolytic production of zinc, cobalt is removed from the zinc electrolyte by cementation with zinc dust prior to electrowinning. Although the thermodynamics for this reaction are favourable, kinetic barriers to cobalt reduction render the method almost useless in practice unless activators such as copper and antimony or arsenic are added. There is a large body of work studying the effect of these additives, yet the mechanism by which they act is still poorly understood. Even when the target conditions are met, zinc dust consumption is excessively high: satisfactory operation requires up to 300 times the stoichiometric amount of zinc dust. The objective of this work is three-fold: (1) to examine the effects of activators and elucidate the characteristics that make a good activator; (2) to identify new additives that could lead to a more efficient purification process; and (3) to test the new additives with synthetic and real electrolyte solutions. The present paper gives a status report on this project.

Jan 1, 1998

By Kazusuke Sato, Takahiro Uno, Koji Hoshino

"A novel Ni coating technique of Ni(OH)2 powders was developed to improve the positive-electrode performance· of the Ni-MH batteries. It was found out that Ni(OH)2 powder was reduced by N2H4 without any catalysts in an alkaline - solution at high temperatures. In result of observation of pH and potential changes in the solution during the reaction, it was found that the reduced species was HNio2- ion dissociated from Ni(OH)2 in the alkaline solution. The molar fraction of reduced Ni of the Ni(OH)2 was increased in proportion to the amount of added N2H4. At the small Ni fraction, a porous Ni layer was formed on the surface of Ni(OH)2 powder. Open cell tests were carried out with the paste type electrodes made of either the Ni coated Ni(OH)2 powder or non-coat powder, and cell performances were compared. In result, it was found that the Ni coating technique is effective on improvement in the utilization of Ni(OH); as a positive-electrode active material under high current densities.IntroductionNi-MH rechargeable battery is generally used for the power source of portable machines and electric vehicles because of its good performance at high energy density and. long term cyclical life as well as cleanness and good safety. Cell component materials have been improved respectively, and as concerns ·the positive-electrode reducing 'the internal resistance is a principal problem to improve the discharging performance at higher current densities.In recent years, improved Ni(OH)2 powders coated with conductive materials as NI. or CoOOH have been developed for the· positive-electrode active materials in order to· reduce the internal resistance of the electrode1)· 2) The Ni coated Ni(OH)2, however, is costly because it is fabricated by .the -non-electrode plate technique which needs a expensive precious ·metal catalyst as PdC12We found that Ni(OH)2 powder was reduced by N2H4 without any cryatalysts in an alkaline solution at high temperatures. After the treatment, Ni(OH)2 powder become gray color like Ni powder from light-green color; and. turned into a magnetic. In this study, the mechanism of the -reducing reaction was investigated to apply the reactions .to a novel Ni coating technique of Ni(OH)2 powders, · and the performance of the Ni coated Ni(OH)2 powder obtained by the reducing process was evaluated as an -positive-electrode active material of Ni-MH batteries."

Jan 1, 2000

By Y. Maeda

Non-ferrous smelting furnaces generally install a gas cooling system for treatment of waste gas containing SO2,. From the point of view of corrosion resistance and recovery of waste heat, the high pressure boiler system is the best way to cool gas, however this system requires high initial investment and relatively higher operating costs. Because the feasibility of this boiler system greatly depends on the smelting process and scale, other lower temperature systems, e.g. water-cooled jacket system, are more suitable if the smelting process does not produce enough steam nor generate enough electricity to compensate operating cost. In additton, the water-cooled jacket system is simple in structure and easy to operate. For those reasons, it is applied widely. A new smelting furnace was planned in our factory and it was necessary to install waste gas cooling equipment. In our case, a water-cooled jacket system was more feasible because of the low gas volume and high dust content. It was also expected to operate without maintenance for ten years. On the other hand, some leakage problems with the water-cooled jacket had been experienced in the past. That is because SO2 In the waste gas changed into sulfuric acid which corroded the jacket material. As the first step, several data from actual&apos; usage were reviewed to throw light on the corrosion process, and an appropriate procedure to determine the operating temperature of cooling water was obtained. For the basis of this study, a water-cooled jacket system was newly designed and tested for three months in a pilot plant. After this system&apos;s performance was confirmed, it was installed in a new furnace as a commercial plant. After one year of operation, the initial thickness of carbon steel jacket remains almost the same.

Jan 1, 1992

By Eiichi Kuzuno, Atsushi Shibayama, Toyohisa Fujita, Kazuo Koike, Toshio Miyazaki, Hitoshi Masuda

"A solid sulfur is more useful to recover and store than a sulfuric acid as a by-product in the zinc hydrometallurgy. In this experiment a zin concentrate (sphalerite) was leached with ferric sulfate at about 373 K for 3 to 6 hours. Zinc was leached more than 95%. After a solid-liquid separation, the leached residue contained solid sulfur was obtained. The particles in the residue were dispersed by lignin and the solid sulfur of approximately 85% was recovered as float product by a flotation with frother in the pH 4. The dried float product was heated at 413K for 2 hours. The pure solid sulfur was recovered. On the other hand in the leached liquid a zinc oxide was ·added and ferrous .iron was oxidized to ferric iron by blowing oxygen. This ferric iron was returned to the zinc leached process after solid-liquid separation.IntroductionZinc concentrate is usually roasted as pretreatment in zinc hydrometallurgy and the produced S02 is changed to sulfuric acid. However, recently in Japan the utilization of sulfuric acid has been limited and it is more costly to store. Instead of producing sulfutic acid the solid sulfur recovery has been examined by direct leaching of zinc_ concentrate in this experiment.In the direct leaching, several kinds of effects have been studied for leaching of sphalerite in ferric sulfate solution. The addition of lignine siilfonate1 • 2) and fine· grinding3) increases the · speed arid leaching fraction of sphalerite. The leaching ratio depends on impurities in sphalerite ores4 • 5). Here, the zinc concentrate is leached ferric sulfate solution under atmospheric pressure at 373K. The solid sulfur in leached residue is separated as float products from other solids by sink-float separation and flotation. The sulfur in float products is purified by evaporation at 413K and recovered."

Jan 1, 2000

By Kim Fagerlund

A novel apparatus for studying refractory infiltration and dissolution/degradation under a temperature gradient was developed. To supersede conventional isothermal refractory testing, a new temperature gradient technique, based on a crucible equipped with a cooling element, has been developed to provide practical information on the penetration and dissolution of refractory materials under cooled conditions. This technique was adopted and applied to several refractory-slag systems. Commercially available magnesia chrome refractory bricks against a copper-containing calcium ferrite type of slag were tested and compared using both a conventional crucible test and the new temperature gradient method. The experiments were conducted at 1300-1420°C under a controlled atmosphere of nitrogen or air. It was noticed that the type of porosity has a significant effect on infiltration of magnesia chrome refractories. Furthemore, the copper-containing calcium ferrite slag caused a severe slag attack and refractory failure in some cases, due to its fluidity and corrosive nature.

Jan 1, 2002

By Georgeta Rata, Cornelia Petroman, Ioan Petroman

"Proper training and education in the field of recycling and waste treatment are inconceivable without the proper teaching of the terminology specific to both recycling (aerospace products recycling, automotive recycling, general recycling, recycling behaviour, recycling schemes, recycling systems, and waste recycling) and waste (characterization of waste, electronic waste, heavy-metal containing waste, monitoring of waste, radioactive waste, solid waste, waste collection, waste conversion, waste recycling, waste reutilization, waste stabilization, waste storage, and waste treatment) in both the students’ mother tongue and in English for Special Purposes (ESP) as a second language (with focus on the structuring of the specific terminology). Including linguistic approaches among the possible approaches of environmental protection and material sustainability means including linguistics among the various disciplines addressing energy supply, cement and building materials, metallurgy, chemistry, glassware, pulp and paper industry, machinery, automobile and electronic industries, collection, and sorting, further treatment and final disposal of post-consumer material.IntroductionCultural and technical changes have produced more novel artefacts than novel activities or novel properties, generating new vocabulary needs that are readily answered by new words (nouns).The purpose of this research is to show that ‘waste words’ – phrasal words (items that have the internal structure of phrases but function syntactically as words, e.g., cattle waste) and particularly compound nouns (words formed by combining roots, that tend to have a meaning that is more or less idiosyncratic or unpredictable, e.g., wastepaper ‘discarded paper’) – used in the study of the English of recycling, waste treatment, and clean technologies can be misleading for both native and non-native students and/or users of English because their structure alone does not allow instant, proper understanding of their meaning.Our hypothesis is that this inconvenient can be overcome by getting to reach the proper meaning of these new words. Or, arriving at the precise meanings of the ‘waste words’ depends on our knowledge of the world (for example, wastepaper indicates that some used paper is discarded and not wasted) rather than on purely linguistic knowledge."

Jan 1, 2008

By Alan J. Hurd

"New insights into the development of microstructure in sol-gel films have recently been revealed by several diagnostic techniques, including imaging ellipsometry, ""chemical imaging"" by fluorescent tracers, light scattering from capillary waves, and finite-element modeling. The evolution of porosity during the continuous transition from dilute sol to porous solid in restricted geometries such as films and fibers is becoming clearer through fundamental understanding of evaporation dynamics and capillarity.IntroductionWith sol-gel processing, the full flexibility of solution chemistry can be exploited to make ceramic films and fibers with well controlled compositional characteristics. No less important is the ability to tune porosity and connectivity for specific applications such as optical and electrical coatings and membranes. Since the chemical and physical factors that determine the microstructure are not entirely understood, new diagnostics applied to sol-gel processing are welcome.Sol-gel films and fibers are distinguished by processing that takes a sol through continuous stages of increasing concentration and connectivity of a solid precursor. The liquid carrier is usually volatile or, at least, volatilizable through heat treatment. During deposition through states of increasing solids concentration, this sol might gel, as in bulk sol-gel processing, however, the gel state may be a fleeting transient that quickly empties of liquid. Nevertheless, the structures formed in solution during this stage influence the structure of the final solid. In particular, porosity is likely to be a remnant of networks formed in the sol-to-gel transition. Here we report on experiments whose goal is to discover the factors involved with porosity development."

Jan 1, 1994