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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 J. N. Hryn, E. J. Daniels, M. Askew, Kirchner. G.

This presentation addresses the changing regulatory climate towards aluminum dross and salt cake in Europe and in the United States. Although sporadic, the trend in the U.S. continues to be away from command-and-control regulation of these materials. This trend began in the early 1980s when the Environmental Protection Agency was successfully sued in court and prevented from classifying dross as a hazardous material. The situation in Europe is different. Because of Council Directive 96/61/EC from the European Commission, European Union member countries have all passed legislation that will essentially cause all salt cake and drosses to be reprocessed. The implementation date of the legislation varies from country to country: from 2001 in the United Kingdom to 2007 in Germany, France, Austria, Italy, and Spain. The European aluminum industry is urging the EC to use the approach adopted by the U.S. EPA, which declassifies the majority of aluminum drosses and salt cakes.

Jan 1, 2000

By Igor Zh. Bunim, Valentine A. Chanturiya, Alexey T. Kovalev, Irina A. Khabarova, Elizaveta V. Koporulina

This paper presents new theoretical and experimental data on possible mechanisms for the formation of micro- and nanophases on the surface of sulfide minerals un der the effect of high-power nanosecond electromagnetic pulses (HPEMP). The gas outflow from nanosecond breakdown channels of sulfide minerals under the effect of HPEMP is considered, with allowance for the condensation of iron vapors. The condensation of matter in an outflowing jet is shown to be an effective mechanism for structureal and chemical transformations of sulfide surfaces. It is established that electrode potential of pyrrhotite is moved together in the negative party owing to formation of iron oxides (hydroxides) and iron sulfates by HPEMP, that provides decrease of xanthate sorption and reduction flotation extraction of this sulfide, whereas electrode potential of pentlandite gets more positive values at the expense of additional formation of element sulfur, that causes increase of xanthate sorption and, as a consequence, increase of nickel sulfide extraction.

Jan 1, 2012

By Qin Li

An highly active absorbent with oxidization based on fly ash, lime and additives was prepared. Experiments of simultaneous desulphurization and denitrification were carried out using fixture bed and duct injection. The influential factors for the absorptive capacity of the absorbent were studied. The absorptive capacities of 120.7mg for SO2 and 43.7 mg for NOx were achieved at a Ca/(S + N) molar ratio 1.2, respectively, corresponding removal efficiencies of 87% and 76%, while spent absorbent appeared in the form of dry powder. The optimal temperature and humidity of flue gas treated with this process were shown to be approximately 50\\176 and 5% respectively. The mechanism of removal for SO2 and NOx was investigated. In comparison with traditional dry FGD, this process appears to have lower cost, less complicated configuration and simpler disposal of used absorbent. The valuable references can be provided for industrial application by this process. The foreground of application will be vast in China and in the world.

Jan 1, 2006

By G. Roy Chaudhury

Adsorption techniques are comparatively low cost and effective for treatment of arsenic contaminated drinking water. Various adsorbents such as alumina, ferrihydrite and manganese ores have been used, but there has been little investigation of modifying the structure of ferrihydrite to improve its adsorptive efficiency of As(III) and As(V). In the present study the incorporation of manganese oxide into the ferrihydrite structure was carried out and the prepared materials used in arsenic adsorption experiments. The compounds were X-ray amorphous, but TGA/DTA and FTIR analysis showed some structural characteristics. Sorption studies reported in this paper indicate the excellent arsenic removal properties of the manganese/iron compounds with a loading capacity of 0.3 mmol/g. Adsorption follows first order kinetics and the results fitted to adsorption and mass transfer models. Arsenic levels in water containing 1 mg/L As(V) were reduced by 50% in 20 minutes and 90% in 60 minutes using 1 g/L manganic ferric oxyhydroxide.

Jan 1, 2003

By James Wang

In July 2003, The Office of Hydrogen, Fuel Cells and Infrastructure Technologies of the Department of Energy (DOE) Office of Energy Efficiency and Renewable Energy solicited Grand Challenge Proposals to establish three Centers of Excellence in hydrogen storage developments for reversible metal hydrides, non-reversible chemical hydrides and carbon storage materials, respectively. The program mission is to research and develop cost-effective, on-board hydrogen storage systems that enable a minimum range of 300 miles within the weight and volume constraints of the vehicle. Currently, no hydrogen storage technology available can meet the DOE cost and performance targets. In April 2004, Sandia National Laboratories was selected by DOE to lead the Metal Hydride Center of Excellence with partners from 5 other national laboratories. We will present the organization and recent accomplishments of the Metal Hydride Center which is confident to accomplish DOE/FreedomCAR and Fuels Partnership objectives for 2010 in hydrogen storage for vehicular transportation applications.

Jan 1, 2006

By Jinqian Zhao, Jiarong Li, Shizhong Liu

"Creep cavitation of in single crystal (SX) superalloy was investigated. The constant load creep tests, in single crystal superalloys DD6, were conducted at the conditions of 800°C/700MPa, 850°C/550MPa and 900°C/450MPa, respectively. It was found that there were square facets on the stress fracture surface, and microscopic cavities in the ruptured specimens in the vicinity of the fracture surface. Both the square facets on the fracture surface and microscopic cavities in the section of the ruptured specimens show the morphology of the same thing at the different views, namely creep cavities, which are take the form of flatten cuboid. In fact, creep cavities are the longitudinally tensiled creep cracks slowly growing during the stress tensiling. The factors of creep cracks nucleation and growth conditions include: (a) enough high temperature to activate diffusion (b) casting pores as nucleation origination (c) high strains and strain rates. Eventually, the instantaneous fracture mechanism of creep specimen is cleavage fracture.IntroductionFor the materials used in elevated temperature service, creep behavior has to be accounted for. It is well recognized that creep rupture in polycrystalline materials at high temperature occurs principally by the nucleation and growth of microscopic cavities at grain boundaries, followed by microscopic cavities linkage to form micro- and eventually macro-intergranular cracks[l,2]. Without the usual grain boundaries, SX superalloys have superior capabilities at high temperatures to polycrystalline superalloys, and have become an established feature of gas turbine technology where they are commonly employed in the manufacture of high performance blades[3]. A considerable amount of work has been done over the past tens of years, and many models for nucleation and growth of creep cavities have been proposed, however, those are mainly for polycrystalline materials.In order to improve creep resistance that single crystal superalloys, in which grain boundaries are removed, have been developed. Because there don't exist grain boundaries in SX superalloy, the mechanism of nucleation and growth of creep cavities must be different from that in polycrystalline materials.Understanding the formation and characteristics of creep cavitation is crucial to model the lives of single crystal superalloys.M. Marchionni and L.G. Zhao et al. found that there were square facets on the stress fracture surface [4,5]. Roger C. Reed pointed out creep cavities lie in the necked region[6]. In this paper, the effects on the formation of creep cavities are discussed, as well as the morphology of creep cavities and fracture mechanism of SX superalloys."

Jan 1, 2013

By Jie Li, Liangxing Jiang, Yexiang Liu, Junfeng Gui, Bo Hong, Xiaocong Zhong, Yanqing Lai, Xiaoying Yu

"Pb-based alloys with Pr and Ag were prepared in vacuum electromagnetic induction furnace. The tensile strength, corrosion rate and anodic potential in sulfate solution were measured, and the experimental data were analyzed according to the metallographic phases of alloys, the micromorphology and composition of their oxide films. The results show that, with the addition of Pr, the ultimate tensile strength and corrosion rate of pure lead were increased, and the anodic potential decreased. The extra addition of Ag can improve the properties of alloy further. Comparing with Pb-Ag0.8 alloy which is widely used in zinc electrowinning industry, the ultimate tensile strength of Pb-Ag0.6-Pr2.0 alloy was increased by 31.75%, the anodic potential under 50mA/cm2 was decreased by 30m V.IntroductionIn zinc electrowinning industry, the Pb-Ag (0.5-1.0 wt.%, 0.8wt.% normally) anode is widely used as an insoluble anode['l. It can meet the basic requirements, but still has several problems such as high oxygen evolution over-potential (about 860mV), unsatisfactory corrosion resistance, lead contamination of the cathode product and high consumption of Ag etc.In order to reduce the energy consumption, enhance the corrosion resistance, improve the product quality and reduce the consumption of Ag (or even dispense with it), much research has been done, mainly focusing on Pb-based alloy anodes and Ti-based coated anodes. Detailed investigations have already been carried out on binary alloys (Pb-Ca and Pb-Co), ternary alloys (Pb-Ag-Ca, Pb-Ag-Ti, Pb-Ag-Sn, Pb-Sr-Sn, and Pb-Ca-Sn) and quaternary alloys (Pb-Ca-Sr-Ag, Pb-Ca-Ce-Ag, and Pb-Ag-Sn-Co)[Z-4l, Although these anodes can effectively reduce the consumption of Ag, only the Pb-Co and Pb-Ag-Sn-Co anodes perform well with regard to reducing the anodic potential. However, their complicated manufacturing conditions restrict further commercial use.Besides its application in nonferrous metal electro-winning industry, Pb-based alloy is also used as grid alloy for lead-acid battery, serving as active materials supporter and current collector. In order to enhance the corrosion resistance and deep-cycling performance, reduce the impedance of the corrosion film, the addition of appropriate rare earth elements into anodic grid alloys has become a research focus. Studies proved that RE can enhance the mechanical strength of grids, inhibit the formation of anodic Pb(II) film on the surface of grids and then reduce the impedance of the film[ 10-12l."

Jan 1, 2013

By Xuewei Lv, Maojun Zhou, Xiaobo Huang, Rende Zhang

"The characterization of the surface roughness of the mineral particles is of vital importance for the studies of the mineral processing. In this study, an evaluation of the roughness of the iron ore particles, with the measurements of size distribution and the measurements of specific surface area with the liquid nitrogen absorption, was developed. The main theory of this method is the fact that the roughness of the particle influences the specific surface area apparently. The specific surface area of the particles can be measured with the laser diffraction method and the liquid nitrogen absorption method. The influence of the surface roughness of the particle can be measured with the nitrogen absorption and cannot be measured with the laser diffraction. Therefore, the roughness can be got by comparing the specific surface area with two measurement methods.IntroductionThe characterization of the surface roughness of the mineral particles is of vital importance for the studies of the mineral processing. There are three main methods for measuring the size distribution of mineral particles: sieving, laser diffraction, and sedimentationl). Many techniques involve sedimentation such as the Horiba2, 3) and the Cyclo-sizer1). In the mineral industry, size distribution is usually determined by sieving because it can be carried out accurately for all particle sizes larger than 45 . The preferred method to obtain the size distribution of finer particles is laser diffractometry. The technique has several advantages: it produces measurements in a few minutes with considerably less labor compared with the cyclo-sizer and for a range of sizes considerably wider in comparison with the sedigraph4). The equivalent-sphere size distribution reported by laser diffractometry is valid for metallurgical calculations and can be routinely used in mineral processing plants. The surface area of the particles can be measured by the BET method of nitrogen adsorption, or it can be calculated from the size distribution. However, the latter calculation requires the size distribution to be accurately known across the whole size range, and assumptions have to be made about the shapes and surface roughness of the particles and presence or absence of pores (see below). The BET method is based on the physical adsorption of gas over the whole exposed surface area and measures the surface area stemming from the roughness and open pores on the surface of the particle5). The calculation of the surface area from the size distribution is usually based on the assumption that all the particles are smooth spheres, without considering the shape and/or roughness of the particles. Determining the surface roughness of the particle with these methods, is the objective of this study."

Jan 1, 2012

By R. D. Osmanson

A series of batch roasting tests was performed on minus 1/2 inch gold bearing refractory samples from the Gold Acres deposit, and 67 select particles were polished and the sulfide alterations were examined microscopically. The suite of specimens represents two hour batch roast treatments at 600°C, 700°C, 725°C, 750°c, 800°C, and 900°C. Auriferous pyrites were found to alter sequencially to pyrrhotite, magnetite and finally to hematite. It was found that the decrease in cyanidation extraction with high temperature roasting is likely due to the increas ing stability of magnetite and more crystalline hematite, and the decrease in porosity with these phases which occlude the gold. Gold has been noted to occur very early in the mineralizing sequence, with gold being found in quartz and in clay/carbonate rock matrix. No gold was found in the two pyrite phases, but numerous gold grains were found in pyrrhotite after pyrite and in subsequent iron oxides. Gold mineralization had apparently ended by the time base metals were introduced into the deposit.

Jan 1, 1987

By Ali Akbar Mottahedi

It is known for a long time that the reaction of oxygen with carbon, silicon, iron and many other elements is exothermic. The heat of released from these kind of reactions can decrease the time of fusion of iron and steel for metallurgical purposes in the electrical arc furnaces. By decreasing the time of fusion, we increase the rate of process and the amount of production. So, by blowing oxygen in to the furnace, we can reduce the consumption of electricity and save cost. There are many problems in the procedure of the oxygen blowing. In this project, the theoretical aspect of the oxygen blowing and its side effects into the arc electric furnaces are investigated. An oxygen blowing system into the arc electrical furnace of metallurgy department of Machine Sazi factory was also set up. This process reduced the consumption of electricity up to 22% and increases the rate of production, by reducing tap ? to ? tap time up to 15%. In this project; all oxygen blowing systems and its control were set up.

Jan 1, 2006

By G. Riverin, C. Simard, W. D. Stevens

"An on-line technique to measure the efficiency of decoating I delacquering processes is being developed by Alcan' s Arvida R & D Centre. Decoating processes are used to remove moisture and coatings from shredded coated material such as Used Beverage Containers (UBC) before melting. Complete removal has been demonstrated to maximize metal recovery. Quantifying the weight of carbon and organic residue adhering to the shred surfaces is very difficult to measure directly, as the material can be highly folded. The technique developed indirectly measures the residue remaining by analysing the concentration of CO evolved in the decoater end zone exhaust gas.A commercial CEMS (Continuous Emission Monitoring System) incorporating an infrared type CO gas analyser was modified for on-line process exhaust gas analysis. Both pilot and plant trials had demonstrated that the CO concentration measured was inversely proportional to the efficiency of the organic removal achieved. As the quality of coated purchased scrap can be highly variable in moisture and organic content, continuous measurement should permit adjusting the feed rate and other decoater process parameters to the quality of decoating required."

Jan 1, 2000

By Yu. A. Grinin, Yu. A. Sannikov, M. A. Lyamina, V. A. Shumskij, L. V. Slobodkin, N. N. Ushakov

This manuscript describes the Kivcet treatment of lead-bearing materials having high contents of copper and zinc. The tests were carried out on bulk concentrates from the Zyrianovsk Mining and Concentrating complex, "Kazzinc" JSC (Kazakhstan) with the following composition: Pb 37.6%, Cu 10.4% and Zn 6.8%. Two properties of the concentrate were under investigation: their calorific value and their desulphurization rate. By adding flux, the charge properties were brought close to the properties of high-grade lead sulphide concentrate. The charge was melted with high productivity. To ensure high copper recovery, Waelz residue was added to the charge. The residue contained more than 20% carbon and about 30% iron metal. The residue was partially replaced by coke that facilitates high copper recovery into the matte. The smelting achieved a production rate of 20 t/h with one burner. Lead recovery into the lead bullion was 88.8%; copper recovery into matte was 92.3%; zinc recovery into slag was 75.5%; and zinc recovery into the fume was 5.1%.

Jan 1, 2000

By Thomas Frost

In this time of market globalization, many industrial companies are including detailed arbitration clauses in their international contracts, in order to avoid the potential costs, delays, and uncertainties of litigation in foreign courts. Arbitration is less expensive and more flexible, procedurally, than court proceedings, and arbitral awards enjoy much greater international recognition than judgments of national courts. More than 134 countries have signed the 1958 United Nations Convention on the Recognition and Enforcement of Foreign Arbitral Awards, known as the "New York Convention", which facilitates the enforcement of arbitral awards internationally. There are several other similar arbitration conventions that provide for the enforcement of cross-border arbitral awards. Additionally, arbitral awards are not subject to appeal, whereas judgments of national courts are routinely subjected to a lengthy appeals process, and there are very few viable bases to challenge arbitral awards. This discussion will review key considerations in drafting arbitration clauses, including choice of law and choice of forum considerations; issues surrounding the selection of arbitrators; the discovery process; presentation of evidence; and enforcement of arbitral awards.

Jan 1, 2006

By Alex Mezei

Experimental rheology data are needed to produce design criteria for mass and energy transfer processes. Large throughput plants operate under continuous flow mode. The capital cost is determined by the accuracy of the rheology data used for design. The operating cost is dictated by the energy required to sustain the flowing conditions of various process slurries. Typically, rheology investigations are carried out during the final stages of metallurgical testwork, which is too late to set the design criteria for the pilot plant. This leads to increased testwork cost, and sometimes lowers confidence in the quality of the data produced. In addition, the engineering and feasibility studies are often delayed because of the lack of pertinent rheology data. One of the objectives of this paper is to emphasize the importance of timely planning and execution of the rheology study, which is shown to be a critical component of the overall testwork program. Various applications are discussed, including elaboration of process and equipment design criteria. In this paper, the emphasis is placed on gold and nickel laterite hydrometallurgy applications.

Jan 1, 2003

By Yotamu Stephen Rainford Hara

"The study focuses on the reduction mechanisms of copper, cobalt and iron during carbothermic reduction of copper-cobalt mineral sulphide concentrates in the presence of lime, in the temperature range of 1073K and 1273K. We have used three types of mineral concentrates which were derived from froth flotation from the Copperbelt region in Zambia. The reduction mechanisms were studied using thermogravimetric analysis in which selected reactions were stopped at different times for characterising the reaction mechanism using optical microscopy, XRD and SEM-EDX analyses. Using SEM-EDX analysis, we have analysed in details the stages of metallic phase formation during reduction process. Metallic cobalt and iron were embedded into copper, thereby permitting magnetic separation of the reduced metals even though copper is diamagnetic. Methods of preferential reduction of metal values were investigated by analysing the metallic phase formation.IntroductionIn conventional smelting or converting of copper sulphide minerals, metallic copper forms by giving off S02 gas on. Although in terms of overall energy balance the selective oxidation for metal production has major advantages, the process suffers from drawbacks in smelting complex concentrates containing copper, cobalt and iron sulphides minerals and these are: (i) cobalt and iron are oxidised, and consequently cobalt is lost into the slag phase. (ii) The volume of S02 gas produced is in low concentrations, which is insufficient for extracting sulphur or manufacturing sulphuric acid. The release of dilute S02 causes serious environmental pollution. The major cause for the loss of cobalt and iron into the slag, is due to that fact that the oxides of these metals are more stable than their sulphides. Since cobalt and copper are more valuable than iron, reducing conditions are required in a separate slag treatment reactor using electric arc melting for recovering the lost metal oxides from slag. This energy-intensive step makes metal making expensive.During chemical beneficiation of mineral sulphides (Cu2S, CoS, FeS) in the presence oflime (CaO), two types of equilibrium conditions may be set up either by forming CaS under reducing conditions, or by stabilizing CaS04 under oxidising conditions [l]. By comparison in the presence of carbon, CaS and metallic phases form, enabling the recovery of metals from sulphide minerals, which have been investigated by a number of authors [2-9]. During reduction of metal sulphide in the presence of lime and with carbon, it has been proven that the overall reaction le proceeds via two main steps: [5, 8, 9] (i) the anion exchange reaction between metal sulphides (MS) and CaO as shown in equation la, followed by (ii) the reduction of metal oxide (MO) via reaction lb."

Jan 1, 2013

By Elizabeth M. Ho

Oxidants are added in uranium leaching in acid media to convert iron(II) in solution to iron(III). Iron(III) has an important role in the leaching of uranium by acting as an electron transfer agent for the oxidation of uranium(IV) to uranium(VI). The oxidation of iron(II) to iron(III) in sulfate solutions using sulfur dioxide/oxygen (SO2/O2) was carried out under typical uranium leaching conditions (pH 1-2, 20-50°C) to confirm literature trends and this work was then extended to the use of SO2/O2 in the leaching of uranium ore. The oxidation rate was found to be dependent on the initial SO2/O2 volumetric ratio and the oxygen mass transfer rate, but was independent of the initial iron(III) concentration above about 200 ppm at pH 2. The presence of 55 ppm organic extractant (Alamine 336) decreased the reaction rate. The oxygen mass transfer coefficient (kLa) for the mixing tank system was measured and was found to decrease with increasing solids density in a 1 g L-1 MgSO4.7H2O solution.

Jan 1, 2003

By Admire Chaendera

A gas jet was blown through submerged nozzles to stir the bath in the presence and absence of slag. Mixing and mass transfer rates were then studied. Water and kerosene (10% by volume) were used to simulate the metal and slag phases respectively in the cold model. The mixing time (Tmix), defined at 99.66% bath homogeneity level, increased with bath height and decreased with an increase in the gas injection rate. Its value in the model vessel was related to gas flow rate (Q), bath weight (W), and bath height (H) by, Tmix = 4.39Q-0.73W0.24H1.12. Inclusion of the slag phase increased Tmix by about 16% and the mass transfer parameter, [(Reloc,r)0.25(Ret)0.32], values by about 32%. Mass transfer rates were higher near the bath surface and in the gas-liquid plume region. They increased with gas flow rate but decreased with an increase in bath height. The relationship, K Q0.08, showing derived mass transfer coefficient (K) dependence on the gas injection rate (Q) was established. The proportionality constant in the equation varied with gas flow rate and sample location.

Jan 1, 2006

By P. Hanniala, J. Sulanto

"The requirement for the reduction of sulphur dioxide emissions from copper smelters is becoming more and more important. Therefore, the most important question in smelting technology will be how to produce even, high strength SO2 gas in smelter and how to combine smelting and converting. The best sorution in certain cases is to eliminate converters totally.Outokumpu is already responding to this challenge. As a result of extensive research work, Outokumpu Oy has developed the Flash Smelting Process for direct smelting of blister copper from concentrates in one step.The newest process development is the Kennecott-Outokumpu Flash Converting process, where solidified copper matte is converted into blister copper. The production of low volume high SO2 content gases, separation of smelting and converting operations to allow increased on-line availability, and simplified process control are the major benefits of the process which translates to reduced smelter capital and operating costs.Also, it has been studied the use of the same Outokumpu furnace for smelting and converting alternately when the production capacity is low.In this paper, the developments and improvements of the Outokumpu Process are described from the operation and investment cost standpoints"

Jan 1, 1988

By K. Koike, N. Masuko, Y. Takasaki

At the Zinc & Lead'95 symposium, one of the authors presented several modifications of Pb-Ag-Ca alloy anodes for the zinc electrowinning process, and also, the behavior of some organic additives in the electrolyte. In this study, the mechanical properties of the electrode materials composed by Pb-0.5 wt% Ag-(0~0.8) wt% Ca were studied by the tensile and Vickers hardness methods. Furthermore, experimental research on the influence of rolling and annealing treatments on the electrolytic behavior and mechanical properties of these alloys was carried out. The tensile strengths of the annealed Pb-0.5 wt% Ag-(0.1-0.8) wt% Ca alloys were the same or higher than those of the as-cast Pb-0.9 wt% Ag alloy. The anode potential using the as-cast Pb-0.5 wt% Ag-0.6 wt% Ca alloy decreased compared to the as-cast Pb-0.9 wt% Ag alloy. Moreover, the annealed Pb-0.5 wt% Ag - 0.6 wt% Ca anode after rolling showed a lower anode potential than the as-cast Pb-0.5 wt% Ag - 0.6 wt% Ca anode.

Jan 1, 2000