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By Ralph P. Hackl

Bacterial leaching of the Doe Run Company?s cobalt/nickel-containing copper concentrate at low pH (pH 1.0-1.2) and high redox potential (>750 mV vs. SHE) enabled the cobalt and nickel to be preferentially dissolved over copper and iron due to the rapid passivation of the chalcopyrite component. Selective leaching of the cobalt and nickel was achieved with a mesophilic culture comprised mainly of Leptospirillum-like bacteria and Acidithiobacillus thiooxidans. This finding led to the conception of a novel hydrometallurgical process for passivating chalcopyrite and recovering the cobalt and nickel. The bacterial leaching process was tested extensively at the bench and pilot plant scales during 1997-1998. A pilot plant containing four leaching stages processed 30-40 kg/day of chalcopyrite concentrate continuously for 87 days. The cobalt extraction ranged from 75% to 86% during 6- and 8-day retention times respectively, whereas the copper extraction was limited to about 9%

Jan 1, 2003

By Sunil Jayasekera

This paper describes the results of a study carried out to examine the feasibility of electrolytic recovery of silver from cyanide leach liquor generated from a Western Australian silver mine tailings using a novel high mass transfer electrowinning cell. The proposed circuit involves heap leaching and electrowinning in a closed loop. The filter-press-like closed electrode arrangement of the cell allowed much improved mass transfer of metal ions to the cathode surface, making direct electrowinning of metals from dilute solutions feasible. The tests were conducted both in the laboratory and at large scale using a prototype with ~1.0 m2 cathode area. The results showed that the recovery of silver from as low as 250 mg L-1tenor was feasible. The silver deposit produced with the prototype cell was non-adherent and powdery and could be readily removed from the closed cell. A system was developed so that silver powder was discharged continuously during the run.

Jan 1, 2003

By Samson Adeosun, Sanmbo Balogun, David Esezobor

"Iron and steel making processes give rise to large amounts of usable and unusable materials, the latter generally being termed wastes. It is sometimes difficult to distinguish between re-usable by-products and wastes which cannot be sold or land-filled. Much depends on circumstances such as the local market for the material. This can itself vary from time to time with by-products which cannot be used or sold becoming wastes and vice versa. This paper defines the concept of “waste-free technology”, discusses its development in the steel industry and highlights the benefits of the technology to the manufacturing sector and the environment. The paper also articulates how the “waste-free” technology could be applied in the proposed Ajaokuta integrated steel plant in Nigeria.IntroductionIn the past, nature was considered an inexhaustible store. Its resources were consequently exploited and waste products therefrom were discarded. Today, attitudes have not changed appreciably even as raw materials cost rise by the year to pose a series of socio-economic problems, which, among others, may include the rational and optimum utilization of resources, environmental protection and reduction of waste formation. Consequently, industrialists now face unexpected regulatory pressure in areas of pollution prevention, waste minimization and hazardous waste disposal.Iron and steel making processes give rise to significant amounts of usable and un-usable materials, the latter generally being termed waste. It is sometimes difficult to distinguish between re-usable by-products and wastes which cannot be sold or land-filled. Much depends on circumstances such as the local market for the material. This can itself vary from time to time with by-products which cannot be used or sold becoming wastes and vice versa. In this paper, the term waste refers to those materials that are either irrationally utilized or, land-filled and part of the byproducts that are not utilized. It includes that part of used materials which is not incorporated into the products manufactured during a process stage and which in contrast to reuseable materials, is considered not suitable for any further use, owing to technical or economic factors. In general, these materials are inorganic and parts of them are either utilized or passed to the other processes; the other part should be disposed of using well-established waste disposal practices to avoid any environmental threat.Thus, creative methods must be developed to modify the manufacturing processes to reduce emissions and process wastes by fully utilizing all resources. One method of eliminating the negative effect of waste formation is the use of purification and cleaning structures (pollution control system, PCS). These are, however, quite expensive."

Jan 1, 2008

By Rod Samuels, Rupert Allen, Thomas Harper

"Viceroy Resource Corporation of Vancouver, B.C., has recently developed and brought into production the Brewery Creek Mine, an open-pit heap leach gold mine, located 55km east of Dawson City in Yukon, Canada. Mineable reserves are 15.2 million tonnes of ore grading 1.45 grams/tonne, containing 22 tonnes (707,315 oz) of gold. Ore processing employs the heap leach technology using run-of-mine ore. Highlights of 1996 activity included construction of a 158,000 m2 of leach pad, placing 1.9 million tonnes of ore at a grade of 1. 46 gpt to the leach pad, construction and successful commissioning of the ADR plant, and pouring of the first gold bar on November 15th.Permitting of this mine has drawn significant attention because of the innovated heap leach technology; although this technology has been proven in other jurisdictions, it has not been used at such extreme northern sites where winter temperatures routinely reach -45°C for extended periods.ABSTRACT ONLY"

Jan 1, 1997

By S. H. Castro

The El Teniente molybdenite plant (Chile), with a nominal capacity of 3,200 tpd of bulk Cu-Mo concentrate, produced approximately 3,385 metric tonnes of Mo during 1998 by using the phosphate Nokes process (LR-744 reagent). This is the only Chilean moly plant which traditionally has depressed copper and iron sulfides with LR 744 reagent, which is a hydrolysis product of P2S5 and NaOH. El Teniente's ore Mo grade is 0.02%Mo and is concentrated to 0.45%-0.50% Mo in bulk Cu-Mo flotation. Subsequently, molybdenite is floated by selective flotation to depress Cu and Fe sulfides, such as chalcopyrite, bornite, digenite and pyrite, to produce typically a 49%-50%Mo molybdenite concentrate. An optimisation program during the last two years was undertaken to improve molybdenite recoveries. Current molybdenite plant technology at El Teniente and use of phosphate Nokes in the process process is reported. Use of phosphate Nokes reagent has increased average Mo recovery from 70.5% in 1977 to a mean 74.7% for the first 4 months of 1999. The global Mo recovery, including bulk flotation, incresed from 42.3% in 1997 to 46.8% in 1998, with a projection of 55.5% for 1999. Mo production per year has increased from 3,181 tons in 1997 to 3,385 tons in 1998 and a projected 4,000 tons for 1999.

Jan 1, 1999

By K. E. Gonsalves, G. M. Chow

"Nanostructured powders (particle diameter of 1 - 100 nm) have uses in electronic, magnetic, structural, thermal applications as well as advanced processing of materials. Among many methods of making nanostructured powders, chemical routes offer many attractive features such as feasibility of cost-effective bulk quantity production, design of chemistry at the molecular scale, and chemical homogeneity of the powders. In this talk, two systems of chemically synthesized nanocomposite powders are presented, namely, granular magnetic materials of Fe-Cu and Co-Cu, and thermal-structural materials of AIN-BN. Synthesis and processing, characterization and properties of these materials are discussed.IntroductionNanostructured powders (particle diameter of 1 - 100 nm) are attractive materials because of many useful properties (e.g. catalytic, optical, magnetic etc.) and processing advantages (e.g. lower sintering temperature) [1]. There are many methods of making nanostructured powders, for example, physical and chemical vapor deposition, mechanical attrition, and solution chemistry [1, 2]. A common method of making composite powders involves the grinding, mixing and blending of constituents powders, but it has the limitation of inhomogeneous mixing. Chemical routes have many useful features. Using solution chemistry, precursors can be molecularly tailored and homogeneously mixed at the molecular level. The chemical approach may result in better properties of the final product. Compared to vapor-phase fabrication techniques, chemical routes are more cost-effective in producing large quantity of material. In addition, control of particle size, size distribution and stabilization of the nanoscale particles against agglomeration can be more effectively manipulated via solution chemistry.In this paper, we present an overview of some of our work in nanocomposite powders prepared by solution chemistry. Metallic systems of FeCu and Co-Cu, and ceramic system of AIN-BN are discussed. The powders were characterized using x-ray diffraction (XRD) , scanning electron microscopy (SEM), conventional and high resolution transmission electron microscopy (TEM, HRTEM), vibrating sample magnetometry (VSM), inductively coupled plasmaatomic emission spectroscopy (ICP-AES)."

Jan 1, 1994

By Norihisa Iida, Yutaka Koshiba, Tsutoipu Masui

"Mitsubishi Materials has many years of experience in the production of oxygen free copper (OFC) and its alloys with a fully continuous-casting process. Four grades of OFC, commercial, electronic, superconductor, and ASTM class I are available according to user needs such as stabilizer for superconductivity, magnetron, and ultra-vacuum systems. Along with Cu-Ag and CuSn, we offer OFC based copper alloys such ·as Cu-Cr-Zr, Cu-Fe-P, Cu-Ni-Si and others, that are suitable for lead frame and connectors. Within the maximum sizes of 260mm X 1050mm for cakes and 385mm diameter for billets, we are very flexible and can adjust the ingot size to customer’s requirements. Other products that we can supply are semi-finished products such as hot rolled sheet, ·forged blank, extruded rod and finished products like mold for continuous casting of steel, ring mold for non-ferrous casting and backing plate for sputtering target.IntroductionMitsubishi Materials Corporation developed mass produced high quality oxygen free copper and. high copper alloy ingots in the 1960's. We produce 60,000 - 70,000 tons annually giving us 22 - 23% share of the world's market.Our oxygen free copper and. copper alloys are produced with a fully continuous casting process using only high-grade copper cathodes from our Naoshima and Onahama refineries. The raw material is melted and cast in' a carefully controlled atmosphere resulting in a product with low impurities and excellent properties.Using a controlled atmosphere it is possible to produce high quality copper alloys including active elements like chromium (Cr), zirconium (Zr), titanium (Ti), and magnesium (Mg) which are difficult to produce using standard batch casting methods.Using our own cakes and ·billets we produce and supply worldwide wrought materials like molds for ferrous and non-femous casting. These products receive special patented thermo-mechanical· treatments resulting in high strength and excellent conductivity with low cost."

Jan 1, 2000

By Junji Shibata

The waste acid mixture whose main component is phosphoric acid, is discharged from the etching process in the liquid crystal production industry. In order to separate impurity acids from the phosphoric acid, trioctyl phosphate (TOP) is used as an extractant. TOP can extract acetic and nitric acids selectivity. The extraction and stripping operations are carried out for the acid mixture by beaker-scale experiments and countercurrent multistage operations with mixer-settler equipment. TOP selectively extracts the acetic and nitric acids in the acid mixture. From the results of the McCabe-Thiele analysis obtained by beaker-scale tests, the extraction for acetic and nitric acids are approximately 100%, respectively, by 6-stage extraction with a phase ratio (A/O) of 0.4. On the other hand, almost all of acetic and nitric acids are stripped with water from the organic phase by 4-stage stripping with a phase ratio (A/O) of 1.0. About 95% of acetic and 98% of nitric acids can be removed from the acid mixture without extracting phosphoric acid in case of the mixer-settler equipment operation. There are several steps such as slicing, lapping, chemical etching and mechanical polishing in the silicon wafer production process. The chemical etching step is necessary to remove any damaged layer caused in the slicing and lapping steps. The typical etching liquor is the acid mixture comprising nitric acid, acetic acid and hydrofluoric acid. The waste acid is treated by a neutralization method with a high alkali cost and balky solid residue. A solvent extraction method is applicable to separate and recover each acid. Acetic acid is first separated from the waste liquor using 2-ethlyhexyl alcohols as an extractant. Then, nitric acid is recovered using TBP (Tri-butyl phosphate). Finally hydrofluoric acid is separated with TBP solvent extraction. The expected recovered acids in this process are 2mol/L acetic acid, 6mol/L nitric acid and 6mol/L hydrofluoric acid. The yields of this process are almost 100% for acetic acid and nitric acid. On the other hand, it is important to recover and reuse the metal values contained in various industrial wastes from a viewpoint of environmental preservation. Most industrial products are made through processes to separate impurities in raw materials, solid and liquid wastes being necessarily discharged as industrial wastes. Chemical methods such as solvent extraction, ion exchange and membrane separation, and physical methods such as heavy media separation, magnetic separation and electrostatic separation are considered as the methods for separation and recovery of the metal values from the wastes. Some examples of the application of solvent extraction to the treatment of wastes such as Ni-Co alloy scrap, Sm-Co alloy scrap, fly ash and flue dust, and liquid wastes such as plating solution, the rinse solution, etching solution and pickling solution are introduced.

Jan 1, 2003

By E. Yegan Erdem, Fiona M. Doyle, Alyssa A. Maich

"There is an expanding interest in synthesizing high quality magnetic nanoparticles, most notably for biomedical applications. Different processing routes have been reported for the synthesis of magnetite and maghemite. However, some ambiguity remains on their precise chemistry, intermediates, and final products, due to the structural similarity of maghemite and magnetite, and the relative ease of redox transitions during synthesis. Here we present the results of TEM, x-ray and electron diffraction, and SQUID studies aimed at characterizing the products from two different reaction systems, thereby clarifying the reaction chemistry. The first system hydrolyzed aqueous FeCh and FeCb chlorides with ammonia in a micro fluidic reactor at ambient temperature; although the reaction product displayed a uniform distribution, it included non-magnetic goethite and lepidocrocite. If the aqueous solutions contained dissolved oxygen, there appeared to be extensive oxidation of Fe(II). The second system thermally decomposed iron (III) acetylacetonate in ether. In prior studies, oleylamine has been reported to serve as both a reducing agent and capping ligand to control particle characteristics; however, our studies revealed little reduction, with maghemite dominating the reaction products.IntroductionMagnetite and maghemite nanoparticles are co=only used in ferrofluids, in medical applications, and in drug delivery. Superparamagnetic properties, along with low cytotoxicity, colloid stability and bioactive molecule conjugation capability, make these nanomagnets ideal for both in-vitro and in-vivo biomedical applications [1]. One of the major constraints on widespread adoption of nanoparticles for these applications is the amount needed. Typical batch synthesis methods produce polydispersed nanoparticles, which require further size selection procedures to isolate the mono disperse nanoparticle population needed for many applications. In order to maximize the yield of usable particles from a synthesis operation, the reaction conditions must be closely controlled. This requires full knowledge of how the reaction conditions control the various aspects of nanoparticle growth. Many methods have been used to synthesize iron oxides, including sonochemical reactions, mechanochemical synthesis, hydrolysis and thermal decomposition. This work examines the latter two methods, focusing on oxidation and reduction of iron."

Jan 1, 2012

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 J. Sjöblom

New copper and nickel processes, flash converting and DON, direct high-grade nickel matte smelting, have been developed in order to replace the conventional and not so environmentally friendly PS-converting process. With a laboratory scale laminar-flow furnace the combustion reactions of sulfidic feed particles can be investigated under simulated flash smelting conditions. In the present study, finely ground and screened feed fractions of a copper matte and a nickel matte were flash oxidized in a laminar-flow furnace. The experiments were carried out using 20, 21 vol% and 75 vol% O2 in nitrogen, at temperatures 1100 and 1300 °C and reaction zone length of 7.5-16 cm. The samples were quenched in a water film after a specified reaction time. The matte particle reactions were stopped after short residence time intervals in order to obtain a better understanding of the reaction mechanisms. Chemical analysis was used to determine oxidation degree, and optical and scanning electron microscope combined with energy dispersive analysis was used for characterization of the reacted particles. On the basis of the experimental results the reactivity of the mattes is discussed and possible reaction and dust formation mechanisms are considered.

Jan 1, 1999

By T. Ranki-Kilpinen

In the flash smelting technique, developed by Outokumpu Oyj, off-gases with dust load are directed into the heat recovery boiler (HRB). As the temperature decreases, metallic sulphates become thermodynamically stable. Sulphation of oxidic particles initiates. The release of heat causes an increase in particle temperatures, and soft sulphated particles can stick to the heat transfer surfaces. Dust accretion may form and cause operational problems. The objectives of the project are to study sulphation reaction mechanisms and kinetics of flue- dust particles under HRB conditions, and get more information for the flue-dust treatment possibilities. The sulphation behaviour of synthetic Cu2O particles (37-53 pm) was studied using a fluid-bed reactor of laboratory scale. The experimental parameters in the latest campaign were oxygen and sulphur dioxide contents of 2.5-10 vol-% 02 and 40-60 vol-% SO2 respectively and temperatures of 600-660°C. Samples were examined microscopically (SEM+EDS) and chemical analysis were conducted. The sulphation rate was found to have a maximum at the certain temperature, which was dependent on the gas SO2 content. Regardless of the level of SO2, a rise in oxygen content promoted sulphate formation.

Jan 1, 2002

By Shilai Yuan, Huimin Lu, Zhijiang Gao, Panpan Wang

"Solvent refining of silicon through using Si-Al melts is a valid method to remove the impurities from metallurgical grade silicon (MG-Si) melt. The thermodynamic behavior of impurities Fe, Al, Ca, Ti, Cu, C, B and P in MG-Si during the solidification of MG-Si was studied based on the available thermodynamic parameters and experimental data. The morphology of inclusions was investigated by Scanning Electron Microscope (SEM). The chemical composition of inclusions in MG-Si and Al-Si melt was analyzed by EPMA. It is found that the amount of white inclusion reduces and most impurities are solved into the Al-Si melts. After solidification of Si–Al alloy using induction heating and acid leaching, impurities can be effectively removed. The solidification of silicon from the Si–Al melt is found to be more effective for purification than general silicon solidification.IntroductionPhotovoltaic energy is one of promising energy resources in a sustainable society because of its inexhaustibility and cleanliness. Although the production and installation of solar cells have increased significantly during the last decade, the cost of solar cell installation is still high. Multicrystalline silicon has now become the main material in the photovoltaic market because of its low production cost and because of the relative high conversion efficiency of solar cells made from this material, which has been studied for a long time [1-3].Electronic grade (EG) silicon (99.9999999% Si) is commonly used as the raw material to produce SOG-Si (99.9999% Si). Silicon produced from the chemical routes restricts the development of solar cells due to environment threaten, high energy consumption and low productivity. Purification of metallurgical grade silicon (MG-Si) is a low cost, environment friendly method. Although several metallurgical processes such as directional solidification, vacuum refining and electron beam melting [4], have been developed, the cost reduction and refining efficiencies for manufacturing silicon is still have to be further optimized.In the purification process, it is difficult to remove boron and phosphorus by the conventional metal refining method. The refining efficiency depends on the segregation behavior of different elements in solid silicon and the liquid phase. The segregation ratios of all investigated impurities were found to be much smaller than the segregation coefficients between solid and liquid Al-Si melts [5]. For instance, the segregation coefficient of B in Si is 0.8 at the silicon melting point (1687K), whereas it is around 0.2 when silicon is solidified from Si-Al melt at 1273K. For phosphorus the segregation coefficient is 0.06 when silicon is solidified from Si-Al melt at 973K°C, which is much less than 0.35 for recrystallization from liquid silicon. Since the segregation coefficient of boron in silicon is 0.8, it cannot be removed by directional solidification."

Jan 1, 2014

By V. A. Bryukvin

A characteristic feature of the macrokinetics of the interaction process is the presence of two specifically defined areas of oxidation which had a linear time dependence. The effect of variables, such as residual sulphur content of the melt, temperature and the oxidation potential of the gas phase, on the macrokinetics of oxidation are investigated. Phase composition and structure of products of solidification of partially oxidised melts and thermodynamic properties pentaining to Cu-S-O melts are used to analyze the macrokinetic behaviour and mechanisms of the interaction. The process of interaction of sulfide copper melts with oxygen may be considered as a disproportional absorption process and its mechanism is based on localized interaction on the surface and inside the melt volume. Superficial processes include also the process of primary chemisorption of oxygen by melts at place of metal-metal donor bonds proceeding with formation of oxysulfide liquid solutions and volumetric decomposition of the latter accompanied by evolution of sulfur dioxide and metallization of sulfide melts. It is the degree of dynamic balance of such interaction processes that determines specific individual features of the macro-kinetics and mechanism of oxidation of sulfide copper solutions with oxygen in the gas phase.

Jan 1, 2006

By K. O. Fagerlund

Theoretically and experimentally determined copper matte settling rate in iron silicate slag has been discussed. Separation and settling rate measurements of sand, homogenised slag and 25%Cu concentrate, 63%Cu industrial, and 71%Cu synthetic copper mattes were carried out by mixing crushed slag and matte samples with silica sand in an alumina crucible and melting at 1300-1350°C. Two different types of slag compositions were employed, with Fe/SiO2-ratio 1.4 and 1.7. The separation rate was followed by taking samples from the .melt. As expected, the settling rate of copper matte in fayalite slag depended on the slag composition, where the increasing silica decreased the matte settling rate. Microanalysis of solidified slags showed that the rate of separation of low grade matte was low compared with high grade matte and the presence of a very small size fraction of matte droplets in slag remained unsettled in stagnant fluid. The production of sulfur dioxide gas inside the molten bath was found to be possible up to a certain iron sulfide content in the matte. Also, copper matte settling rates in industrial furnaces have been discussed.

Jan 1, 1999

By Deepu Philip, Pratik Agarwal, Ajay Kumar Shukla, Ishani Shukla, G Rajesh

Steel plants generally employ static BOF end point control models to arrive at a given temperature and chemistry at the end of blow. These end point models have now been supplemented with chaos control models to steer the blowing process in the right direction while the blow is in progress. Merely arriving at the correct end point temperature is however not adequate because in the subsequent stages as well the temperature variations can be large and unpredictable. The present paper deals with an integrated model to take into account the effect of all parameters affecting temperature and composition from tapping to the start of casting to minimize the use of LF or aluminum heating, and also minimize grade mixing. The application of lean operations strategy is explained in which the previous “Push System’ is changed to a “Pull System”, minimizing the use of ladle furnace or aluminum heating during steelmaking.

Jan 1, 2014

Most of the world's zinc metal is produced via the roast- leach-electrowinning (RLE) process. The process is well established, but most of the sulphur in the sphalerite concentrates reports in the acid, which has to be stored and/or sold. There are significant incentives to develop a simpler process with much reduced acid generation. Ferric ion is a well known oxidant for most sulphides, in particular sphalerite, and it converts the sulphide to elemental sulphur. Based on stoichiometry, however, the amount of ferric ion needed to achieve acceptable zinc extractions is prohibitive for downstream zinc recovery from the leach solutions. The process suggested here makes use of less-than-stoichiometric ferric sulphate additions because the ferric ion is regenerated by sparging SO2/O2 mixtures. This regeneration can be effected in-situ in the leach vessel or outside the leach vessel. An example of the application of this new process is presented for a Canadian sphalerite concentrate assaying 60% Zn. The effects of temperature, ferric concentration and ferric ion regeneration are presented. Options to recover zinc from the leach solution are also briefly discussed.

Jan 1, 2000

By Yong Hack Lee

Nonferrous smelting processes have been through a rapid transformation since the beginning of 1980. The copper smelting technology has changed from the conventional Blast Furnace process to the Flash Smelting and MIB process. In the field of lead smelting, the technology has changed from the Blast Furnace Smelting to the Direct Smelting such as QSL and KIVCET. In 1992, Onsan Refinery successfully commissioned Direct Smelting QSL technology for lead. The QSL could produce more than 160,000 ton per year of lead bullion from lead concentrate and various residues. Moreover, since the year 2000, the TSL (Top Submerged Lance) Technology utilizing the same Direct Smelting process has been successfully commissioned to treat lead concentrate as well as lead sulfate residue produced from a hydrometallurgical zinc plant. This paper presents and compares the energy flows of lead smelting processes such as a conventional process and the Direct Smelting Processes plotted on the Pb-O-S phase diagram. The oxygen potential diagram suggests how to control the oxygen potential in the furnace. Also, it describes the recent operational experience in the TSL plant of Onsan Refinery with necessary mass balance of key elements.

Jan 1, 2003

By K. Abe

Onahama Smelter has two green-charge reverberatory furnaces and the annual smelting capacity is 600 thousand tons copper concentrate. In addition to the concentrate, various kind of industrial wastes has been processed and utilized. First, the brick waste from converter is ground and used as raw material of castable for repairing the copper melt launders. Second, the slag containing calcium-sulfide from other foundry is fed to the reverberatory furnaces. Calcium sulfide is oxidized to CaO. The melting rate of concentrate is accelenlled and the slag loss is decreased. Third, the tip tire made of waste car tire is charged into the reverberatory furnaces as fuel. The steam of waste heat boiler for turbine generators has been increased so as to decrease the electricity cost. Fourth, the sulfur accretion from other chemical plant is blended into the copper concentrate and the sulfur is recovered as the gypsum for sale. Fifth, the processed waste oil has been utilized in the copper concentrate dryer by which the smelting capacity was increased effectively. Consequently, Onahama smelter contributes to the society by processing the wastes to the harmless slag and utilizing them as fuel through the copper smelting.

Jan 1, 1996

By Joel F. Flurnerfelt

Molten Al and Al alloys containing si, Mn, Ti, and y have been lanced with nitrogen-bearing gases. These lancing experiments provided the means for observing what phases form during exposure to nitrogen-bearing gases for finite periods of time, <2 minutes, at high temperatures, >1290oC. The experiments were conducted in sn induction heated drop tube furnace apparatus. The overall premise of these experiments was to select those Al alloys and gas compositions that show promise of forming secondary dispersoid phases, particularly AIN, in the Al matrix. The alloys selected will be atomized using gas atomization reaction synthesis (GARS) using the most favorable conditions. In this case, the chosen Al alloy will be atomized with a nitrogen-bearing gas, such that the Al and gaseous nitrogen species react to form a dispersoid phase within each powder particle. The powder particles that result from this "aggressive" GARS-process would be essentially Al metal-matrix composites within a uniform distribution of dispersoids. To date, only high-purity Al has been atomized using a mild GARS reaction. This work is funded by the Materials Science Division of DOE-BES under contract number W-7405-Eng-82.

Jan 1, 1996