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By Chunlin Chen

Published data on thermodynamics of a number of minor elements (As, Sb, Bi, Pb, Zn, Se, Te, Cr, Sn) in liquid copper, matte and slag have been reviewed, assessed and used in development of thermodynamic solution models of melts. The behavior of antimony in alloys, mattes and slags is used as an example to illustrate the approach taken in assessment of published data and validation of the developed models with respect to the activity of Sb in condensed phases as well as the effects of matte grade, slag chemistry, temperature etc on the equilibrium distribution of Sb between melts and the gas phase. Results obtained from a comparison of different smelting processes with the modeled multi-phase equilibrium are presented and discussed. The predicted effects of slag chemistry and matte grade on the deportment of other minor elements during smelting of copper mattes will be presented and discussed.

Jan 1, 2006

By S. S. Chabot, S. E. James

A recent survey of major steel companies worldwide revealed the importance of recycling zinc units from electric arc furnace (EAF) dust, mill scale, blast furnace dust and other zinc containing streams within the steel industry. Many processes have been developed and installed in response to this challenge. The most successful approach involves the production of a crude zinc oxide and its sale to primary zinc producers to recover the metal values. The problem with this process is the high concentration of halides in the crude oxide. This type of material cannot be processed directly in an electrolytic zinc plant because of the corrosion problems it will cause in electrolysis. In 1999, Big River Zinc installed a zinc oxide receiving and washing plant to minimize the impact of halides in its electrolysis circuit. A description of the washing plant and the initial operating results are presented in this paper.

Jan 1, 2000

By D. N. Wilson

The potential risks of working with lead have been recognised for centuries, but it is only with the development of sensitive measuring techniques in relatively recent years that it has been possible to establish effective approaches for the monitoring and control of lead exposure. This paper examines the principal control measures employed today - lead in air and lead in blood - and reviews the evolution of numerical standards, with particular reference to the latest understanding of health effects. In addition to lead, a large number of other metals are commonly encountered when producing lead and zinc - both primary and secondary - and the health effects of many of these are discussed. Modern hygiene practices and technologies, which have proved successful in reducing worker exposures, are reviewed. The paper concludes with a look at how exposure standards are likely to change in the near to medium future

Jan 1, 2000

By Yoshisada Michiura, Junko Umeda, Katsuyoshi Kondoh

Rice husks or straws, one of the main agricultural wastes in South-east Asia, have a large possibility to be employed as usefully renewable resources to produce energy and high-purity silica (SiO2), because they consist of about 70% organics such as cellulose or hemi-cellulose, and 20% amorphous SiO2. The former is utilized as bio-mass energy; for example, thermal or electric energy, and bio-mass ethanol. High-purity silica can be used as raw materials in the industrial uses. It would be possible to extract silica elements from rice husks and straws by burning them in air because their main contents are organics. In the previous studies, a strong acid leaching treatment on rice husks before burning was carried out by using H2SO4, HCl and HNO3 to prepare high-purity silica materials. This was available to accelerate the hydrolysis of celluloses and hemicelluloses contained in rice husks, and remove the above metallic impurities. A strong acid leaching treatment, however, is significantly hazardous to environment and human life, and causes an increase of the process cost. In this study, the environmentally benign, harmless to human and economically effective process to produce high-purity amorphous SiO2 materials from rice husks has been established without using strong acids. From a viewpoint of the harmless influence on human body, the carboxylic acids were used in the leaching treatment on rice husks. TG-DTA measurement and GCMS analysis indicated that the leaching was effective for the hydrolysis of celluloses and hemicelluloses contained in rice husks at 473K~873K, which produced the same results in using the conventional sulfuric acid. The metallic impurities could be also removed from the husks via a chelate reaction between carboxyl groups (-COOH) and the metal elements. In particular, it was clarified that cadmium (Cd) were completely removed from rice straws by this reaction. Concerning the burning conditions of rice husks after the acid leaching, it was necessary to supply a suitable amount of air to completely combust organics; for example it required air supplement of 50 ml/min. or more. The burning temperature should be less than 1273K to obtain amorphous structured silica. High-purity amorphous silica materials with 99% or more were prepared from rich husks by applying the citric acid leaching treatment and burning process at 1073K in air.

Jan 1, 2008

By Ryosuke Matsuoka

Keywords: Tantalum capacitor, Scrap, Recovery, Titanium, Chlorination A recycling process for tantalum from capacitor scraps using an oxidation process followed by mechanical separation and chemical treatment was investigated. This study demonstrates that sintered tantalum electrodes inside the capacitor scraps can be mechanically collected after the oxidation of the scraps in air, and high-purity tantalum oxide powder (Ta2O5) was efficiently recovered after chemical treatment. By reducing the Ta2O5 obtained through magnesiothermic reduction, tantalum powder with 99 mass-% purity was obtained. Using the chlorination for tantalum recovery was also investigated, and the tantalum or tantalum compounds were reacted with chloride wastes such as FeClx. It was found that tantalum was effectively separated and purified when tantalum powder is reacted with FeClx at 1100 K under an argon atmosphere. This recycling process utilizing chloride scrap has now been extended to other reactive metals such as titanium.

Jan 1, 2004

By I. U. Onyenanu, C. E. Ilochonwu, E. I. Nwonye, C. O. Nwajagu

This work shows how pure silica was derived directly from rice husks ash (RHA) in different temperatures for reduction to Silicon (Si). The processes to form Si materials are usually complex, costly and energy-intensive. The silica in the ash undergoes structural transformations depending on the conditions of combustion. A high purity silica was produced at 650oC after burning the rice husk (RH) for up to 7 hours. The purity of the silica was determined by dissolving the RHA with alkali solution to form sodium silicate solution of pH 11.0. This was added to hydrochloric acid of pH 1.5 which lowered the pH of the solution to 4.0 to form silica gels. The silica gels produced were washed and dried to powder and then characterized using XRD and EDX techniques. This study was done to reduce energy waste and environmental pollution in Nigeria as silica is used to develop many materials.

Jan 1, 2015

By Aliye Arabaci

In the present investigation, an attempt has been made to study the reduction behavior of composite pellets consisting two different types of iron oxide fines (high and low grade) and coke or lignite fines as reducing agents. The reduction experiments were carried out under isothermal conditions and constant flow of nitrogen gas in the temperature range of 900 ? 1100 oC. The variables investigated are the reduction temperature, Cfix/Fe3O4 ratio, reduction time and reductant type. In the experiments carried out with Sivas Divrigi A head magnetite ores (high grade) at a temperature of 1100 oC, for 40 minutes and on the condition that Cfix/Fe3O4 ratio is 0.2, in which lignite and coke fines were used as reductant, degree of reduction was obtained as 91 % and 86 %, respectively. Whereas, in the experiments realized with Malatya-Hekimhan-Hasançelebi magnetite ores (low grade) on the same conditions by using lignite as the reductant, around 60 % degree of reduction was found.

Jan 1, 2008

By Peter Willbrandt

Norddeutsche Affinerie's routes date back to the 18th century. NA was established in 1866 as a joint stock corporation. NA's core business covers the production of copper cathodes from primary and secondary raw materials and the processing of them into wire rod and shapes. Part of the shapes are processed into pre-rolled strip and shaped wires within the Group. With some 3,200 well qualified and highly motivated employees, the NA Group produces some 560,000 tonnes of copper cathodes, 370,000 tonnes of wire rod, 230,000 tonnes of shapes, 130,000 tonnes of pre-rolled strip as well as 70,00 tonnes of strips and shaped wires annually. NA's product range is complemented primarily by precious metals, selenium, sulphuric acid, lead and nickel sulphate. The paper will give an insight into the performance of NA and its business units with regard to production, environmental and health protection and occupational safety.

Jan 1, 2006

By Bahram Rezai

Fine particles float poorly and less-selectively under normal flotation conditions. One of the promising methods for fine minerals is the utilization of the principle of Flocculation. Hydrophobic flocculation flotation (or floc flotation) was tested on a magnetite concentrate that was finely ground to be micron particles, for producing a concentrate with sulphur grade less than 0.1%. After that, slurry dispersing with water glass as dispersant, pyrite fines were subjected to hydrophobic flocculation induced by xanthate and a small amount of kerosene then the slurry was transferred to a flotation cell for recovering the hydrophobic flocs. The experiments carried out indicated that through one-step rougher and two-step cleaner flotation, sulphur grade was reduced from 1% to 0.1%. It has been found that the separation efficiency of the floc flotation process closely correlates with the main parameters of hydrophobic flocculation such as xanthate addition, conditioning time and kerosene addition.

Jan 1, 2006

By K. Eto, H. Akiyama, T. Iwamoto

The Hikoshima smelter carried out an expansion project in 1997 and increased its production from 59,200 t/y to 71,000 t/y. The leaching process and the casting process had production capacities of 84,000 t/y, but because of the electric power situation in Japan, the production capacity in the electrolysis process was limited to 59,200 t/y to justify the production cost. Electrolysis was the bottle neck of the plant. In order to eliminate a part of this bottle neck, and considering the electric power situation in Japan, a way to increase the production during the time when the electric power rate is low was sought. In practice, we increased the number of cells by 36, and further improved the operation procedures in the cellhouse. For example, we improved the working efficiency of the cells, improved the productivity during the night time, decreased the unit power consumption and improved labor productivity. Accordingly, this paper describes the recent operations at the Hikoshima plant.

Jan 1, 2000

By R. W. Lee

The first prototype plant using the Imperial Smelting Process commenced operation in 1950. It is timely therefore to review the developments that have occurred with the process over the past half-century. A major advantage claimed initially for the process was its ability simultaneously to recover zinc and lead from bulk concentrates. This has remained a fundamental advantage, but it has been extended by the increasing treatment of secondary materials containing zinc and lead. This has been facilitated by the development of hot briquetting and tuyere injection. These techniques and their impact on the technology of the operation will be described. The other major advantage claimed for the process was its potential to achieve new levels of productivity in the pyrometallurgical smelting of zinc. This has been realised with operating furnaces producing up to 400 t/d of zinc. The technical developments that have enabled this scale of operation will be reviewed.

Jan 1, 2000

By Chang-hong Peng

Solubility phase equilibrium in the ternary system of Me2+-NH4+-SO42--H2O (Me2+ represented Mn2+, Zn2+ and Fe2+) was studied by the isothermal method at 298K and physicochemical properties of the saturated solution such as density, refractive index and pH were also investigated. The experimental results show that the solubility isothermal phase diagrams of these systems consist of three invariant branches, two invariant points and three crystallization fields. Corresponding to the three crystallization fields, there have three phases of solid, that is MeSO4?nH2O, (NH4)2SO4 and (NH4)2Me(SO4)2?6H2O, respectively. At the eutectic point, the concentration and the refractive indexes of the saturated solution change evidently. Otherwise, the pH value change slowly in all the systems. The calculated results of the density and refractive index agree with the experimental results.

Jan 1, 2006

By Hirokazu Narita

The extractability for Pd(II) using MOTDA and DHS and their durability against a mixed solution of HNO3 and HCl was investigated by solvent extraction and FT-IR measurements. Both MOTDA and DHS selectively extracted Pd(II) over Pt(IV) from 0.75 M HNO32.25 M HCl solutions. The extraction rate of Pd(II) with MOTDA was much greater than that with DHS. In the durability test, the extraction percentage of Pd(II) and the FT-IR spectra were measured using MOTDA and DHS after stirring with 0.75 M HNO32.25 M HCl solutions. The extraction percentage of Pd(II) with MOTDA hardly changed during the two-month stirring; however, that with DHS decreased with an increase in the stirring time. The FT-IR spectra showed the sulfoxide formation by the oxidation of the sulfide in DHS, but not in MOTDA. Consequently, it was found that MOTDA is more durable than DHS.

Jan 1, 2006

By John M. Rapkoch

In the continuing search for copper matte converting methods, commercially available and feasible choices remain Peirce-Smith Converters, Hoboken Converters, Mitsubishi Converting, Ausmelt converting, and Outokumpu/Kennecott Solid Matte Oxygen Converting (?Flash Converting?). While each alternative improves on Peirce-Smith Converters? limited fugitive gas capturing capability, the Peirce-Smith Converter is relatively easy and economic to operate and has an unmatched ability to accept valuable but difficult-to-handle material such as scrap anodes and purchased scrap copper. Recent experience with designing, building, and starting up an ISASMELT facility, applied in primary smelting of copper concentrates, has led the authors to speculate on how suitable the ISASMELT process would be for copper converting, given its low fugitive gas release and its ability to accept a variety of feed types. This paper reviews the potential metallurgical challenges posed by converting copper matte in an ISASMELT vessel and considers possible engineering and design challenges posed by the inclusion of this technology into a new or refurbished copper smelter.

Jan 1, 2006

By Jeffrey Shepherd, Scott R. Smith, Eduard Guerra

"Electrochemical and spectroscopic evidence for the dissolution of a Au electrode by meso-2,3- dimercaptosuccinic acid (DMSA) from an acidic LiCl04 electrolyte is presented. Near the potential of zero charge, DMSA was determined to form a stable layer on the metal surface but at more anodic polarizations, DMSA was displaced from the metal through an oxidative process. The anodic displacement of the layer from the electrode resulted in a small amount of Au that was detected in the electrolyte using atomic absorption analysis. The extent of Au dissolution, was monitored while holding the potential of the electrode for 24 hours at the thermodynamic Eo/H,O in LiCl04 electrolytes containing 10 mM DMSA. This routine resulted in detectable quantities of a soluble Au-DMSA complex in the electrolyte and the greatest leaching was observed at a pH = 2.0. At room temperature, the leaching rate was stable at 10.9 µg cm·2 hr·' however, upon increasing the temperature to 50.0°C, the rate of Au dissolution increased yielding an average rate of extraction of 40.1 µg cm·2 hr- 1. Interestingly, after the first 12 hours of leaching at 50.0°C, the leaching current decreased dramatically suggesting surface passivation which prevented further Au extraction. The implications of this process in the industrial leaching of Au will be discussed.IntroductionThe use of cyanide in the industrial process of leaching Au from ores has raised concerns regarding both operational safety and environmental issues surrounding the disposal of spent leaching eftluents in tailings ponds. Depending on the chemical nature of the processed ore, the spent solutions that are released into the tailings ponds can contain toxic cyanide, either dissolved or complexed with different metals and may pose serious risk to wildlife as well as freshwater contamination to nearby water systems. Because of these issues, some recent studies have focused on the exploration of more environmentally-friendly molecules to selectively leach Au with appropriate kinetics. However, to effectively leach Au into an aqueous solution, a suitable ligand that reacts to form a stable chemical bond with Au is needed to form soluble Au complexes that can be later recovered [I]. Recently several sulfur bearing alternatives have been shown to leach significant quantities of Au in aqueous solutions. These include thiourea [2], thiocyanate [3], and thiosulphate [4]. However, alkylthiols are also known to quickly form a stable covalent Au-S bond [5], but have been relatively understudied in term of their ability to leach Au in solution, even though some short chain thiols are water soluble and relatively nontoxic."

Jan 1, 2012

By Kai Tang, Casper van der Eijk

Natural gas has been used as reductant in the production of iron for several decades. Recently, the use of natural gas as reductant for other metals has been drawing attention because of the low price of natural gas, as well as the reduction of CO2 emissions compared to the use of coke and coal. In this work, the reduction of a mixture of Ti- and Ni-oxides by natural gas has been studied. Within the Ni-Ti system, the intermetallic compound Ni3Ti is thermodynamically the most stable one. Therefore, powders of Ni-oxide and Ti-oxides were mixed in an atomic ratio of three to one and subsequently pelletized. Reduction was performed in a TGA furnace at constant temperature with varying reducing gas atmospheres. In a natural gas containing atmosphere, the Ni-oxide was easily reduced to metallic nickel while the Ti was reduced to Ti-oxycarbides or Ti-oxynitride when nitrogen was present. Depending on the process parameters, several percent of Ti was dissolved in the nickel-based solid phase.

Jan 1, 2014

By Th. Probst, M. Reuter, H. Orbon, U. Boin, J. Vonken, P. Vonk

Although secondary aluminum industry is well established in the world, the recycling process still requires further development to adequately control the process for a higher aluminum yield and a better product quality. In the present paper, recyclabilities of different aluminum scraps have been experimentally studied. Four types of commercial scraps were characterized and melted at 800 - 900 °C to recover 'aluminum metal with the protection salt flux of NaCl-KCl-Na3AlF6 under nitrogen atmosphere. According to the results, the difficulty of recycling aluminum scrap depends on the cleanness and the ratio of surface area to body volume. More non-metallic contaminates and higher ratio of surface area to body volume usually led to a lower metal yield. Usually cast ingots gave better results than rolling mill cuttings under similar conditions. Bottle caps can be recycled more easily than the margarine foil. The effect of temperature was not as significant as the composition of salt flux. The addition of cryolite was essential for a better metal recovery, especially for the scraps with higher surface area. Recycling

Jan 1, 2000

By James D. Navratil

The mineral magnetite, or synthetically prepared iron ferrite (FeO?Fe2O3), has been used to separate a wide variety of substances, such as dissolved metal species and particulate matter, from wastewater. In the absence of an external magnetic field, activated magnetite readily adsorbs numerous metal species including actinide elements. In the presence of the external magnetic field, enhanced capacity was observed in using supported magnetite for removal of actinides and heavy metals from wastewater. The enhanced capacity is primarily due to magnetic filtration of colloidal and submicron particles along with some complex and ion exchange sorption mechanisms. The removal of the magnetic field and use of a regenerating solution can easily regenerate the loaded magnetite. The process has recently been tested for the removal of other metal ions including cobalt and iron. This paper will review previous work on the use of iron oxides for wastewater treatment and discuss the development and potential of the magnetic filtration/sorption process for wastewater treatment applications in hydrometallurgy.

Jan 1, 2003

By Joachim Lemke

The stainless steel sheets of permanent cathodes at Norddeutsche Affinerie (NA) were damaged by corrosion after nearly 11 years in operation. The necessary raising of the strength for stripping the copper had increased the deformation of the stainless steel blades. Current efficiency declined. After investigating the possibilities, like buying new cathodes or treating the steel surface, i.e. by sliding, a repair process was developed whereby the stainless steel sheet was exchanged. Special laser technology for cutting used blades und welding new stainless steel sheets underneath the used hanger bar was applied because the energy input into steel is the lowest of all welding methods. The new stainless steel sheet was welded with the rolling line in a horizontal direction. The achieved flatness of the repaired cathode blades amounted to less than 4mm per meter. During 11 months NA repaired nearly 36,000 permanent cathodes and put them back into operation. Repair costs were much lower than the costs of buying new ones and current efficiency increased again to more than 96% with a current density of 340 A/m².

Jan 1, 2006

By Brady Butler

Many high capacity metal hydrides exhibit a high degree of stability in the hydrogenated state. This stability leads to a number of significant design problems with regard to the low temperature kinetics and thermodynamics of dehydrogenation. Nanometric metal hydride materials provide a promising route for increasing the reaction kinetics while altering the thermodynamic stability of the material. The use of nanometric metal hydride materials for hydrogen storage has largely been absent because of the difficulties associated with the synthesis of these materials. In this paper, research results on the synthesis of lithium based metal hydrides by vapor phase reactions are presented. The lithium based compounds that have been made in our lab include nanosized powders of metallic Li, Li₃N, LiNH₂ and LiH. The vapor phase process has also been used to custom engineer Li-based materials with other alloying elements or doping elements. The dependence of the characteristics of these materials on synthesis process parameters is studied. The effects of nanoscaled particle sizes on the kinetics of dehydrogenation and hydrogenation reactions are also explored.

Jan 1, 2006