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By Guangliang Wu, Dong-chang Huang, Xin-bin Liu

High temperature mechanical properties of 50Cr5MoV roll steel was investigated by Gleeble 1500 thermal simulator testing machine The morphology, composition and microstructure of fracture surface were observed and analyzed by OM, SEM and EDS The results are indicative of that, there are two brittle temperature zones of 50Cr5MoV roll steel at the temperature of 600°C~950°C and 1300°C~1450°C, respectively. The section shrinkage rate is less than 60% The fracture mode changes from mixed ones dominated by intergranular to toughness transgranular one with the increase of temperature at the range of 650°C~1300°C. The fracture is along the solid--liquid phase at the range of 1300°C~ melting point It is crucial to formulate the 50Cr5MoV casting technology, to prevent the cracks and improve the quality of 50Cr5MoV roll steel.

Jan 1, 2016

By T. T. Chen

Canadian Electrolytic Zinc has developed the "cement-stabilization of jarosite residue" Garofix) process to stabilize zinc plant jarosite residues for disposal. The cement-jarosite mixtures cure quickly, have good mechanical strength and low hydraulic permeability; they possess good neutralizing capability and chemical stability. In the jarofix process, Portland cement partly decomposes jarosite to form (SO4MOH)12.nH2O, ferric hydroxide and an alkali sulphate. Approximately 40% of the jarosite reacts in mixtures containing 30% cement. The jarofix product also contains various Ca-Al-Fesilicate-sulphate-hydrate phases and gypsum, which bond the individual particles together imparting mechanical strength and reducing the permeability. Most of the reactions take place in the first few hours of curing. Ammonium jarosite is slightly more reactive than sodium jarosite but releases NH3 gas; water-soluble Zn in the jarosite residue is stabilized in the cement reaction products.

Jan 1, 1996

By A. Kontopoulos

Refractory sulfide gold ores or concentrates require an oxidation pretreatment step to yield the contained gold amenable to the subsequent leaching step. The process options for oxidation pretreatment can be broadly classified as follows: roasting, high or low pressure oxidation bacterial oxidation, chemical oxidation, each with a number of alternative suboptions. Roasting and high pressure oxidation are being applied on an industrial scale; the stage of development of the other options range from preliminary laboratory to advanced pilot plant- In this paper, the major technical, environmental and economic aspects of the above processes are being discussed. Future industrial trends will also be considered. Particular emphasis will be placed on the treatment of arsenical ores and concentrates, where safe plant operation as well as, handling and disposal of the arsenic containing products and/or effluents 'and residues is of paramount importance.

Jan 1, 1990

By Eoghan T. M Doyle

Oxide mixtures of nickel (NiO), cobalt (COO) and chromium (Cr203) were prepared with graphite in stoichiometric amounts and the powder mixtures were compacted to produce cylindrical pellets. The composition of chromium oxide in these mixtures were varied. Pressed pellets were reduced in a flowing stream of argon-4% hydrogen gas (500 ml/min). Both slow and rapid heating methods were adopted to raise the temperature of a pellet during reduction of oxides to form superalloy powder. The reduction temperature was varied between. 1523 and 1623K. The effect of heating rate and niobium oxide addition on the microstructure of the superalloy produced was studied by using ordinary light and scanning electron microscopes. New phases formed as a result of reduction were identified by X-ray powder diffraction technique. The mechanism of reduction of oxides together with the microstructure of NiCrCo alloy are discussed. The thermodynamics of formation of ternary alloy phase is elucidated on the basis of binary phase equilibria and Gibbs free energy of mixing data for the constituent alloy compositions.

Jan 1, 1992

By Lucas L. da Costa, Sergio N. Monteiro, Romulo L. Loiola, Tammy G. Rodrigues Portela

"The fibers extracted from the petiole of the buriti palm tree are relatively strong as compared to other lignocelluloses fibers, with a potential for composite reinforcement. In this work, polyester matrix composites incorporated with these fibers were investigated for their flexural behavior. Specimens with up to 40% in volume of continuous and aligned buriti petiole fibers were bendtested until rupture. The results showed an increase in both the composite mechanical strength and the stiffness with incorporation of these fibers. A fractograph analysis by SEM disclosed a moderate adhesion mechanism between the buriti petiole fiber and the polyester matrix. This mechanism is apparently responsible for the improved performance of the composites.IntroductionIn recent years, the substitution of energy-intensive synthetic materials for natural ones is being considered in many industrial sectors including automobile, packing and textile [1]. A typical case is that of natural fibers, mainly those obtained from cellulose-based plants also known as lignocelluloses fibers. They have being investigated in the past two decades, aiming to replace synthetic fibers, particularly the glass fiber, commonly used as polymer composite reinforcement [2-8]. From the engineering point of view, lignocellulosic fibers present today important environmental, economical, societal and technological advantages already discussed [7-8]. Moreover, several lignocellulosic fibers are known since the beginning of our civilization and still cultivated or naturally extracted all over temperate and tropical regions of the world. According to Kalia et al [1 ], these fibers can be classified by their origin, as shown in Table 1."

Jan 1, 2011

By Niko Hellstén

To capture efficiently the valuable trace metals from nickel slag using electric furnace, it is important to study their distributions between the slag and metallic phases in the furnace. It is impossible to calculate accurately these distributions without experimental measurements. Therefore, in this work, selected trace metal distributions and phase equilibria between K2O containing iron-silicate slags and a metallic Ni-Fe-Cu alloy in nickel slag cleaning furnace conditions were studied. The experimental method developed and applied during the work, involved a modified quenching technique that included equilibration of the samples in semi-sealed quartz ampoules in an inert atmosphere and metallic Fe saturation. The use of the semi-sealed quartz ampoule prevents the escape of volatile elements from the sample during equilibration. Chemical compositions of the phases and the trace elements were analysed by EPMA. From the measured compositions, the trace metal distribution coefficients between the molten Ni-Fe-Cu alloy and slag were calculated.

By Zhou Shu-cai

"A method has been proposed for the pre-treatment of high phosphorus iron ore by carbothermic reduction assisted with microwave irradiation and magnetic separation on a laboratory scale. Chemical analysis of the reduced ore sample, the metal sample and the slag sample were conducted. Based on the above research, the influences of carbon addition, microwave power and microwave irradiation time on the recovery of Fe and dephosphorization were discussed. It indicated that the increase of microwave irradiation time and power had substantial effect on the recovery of Fe while the influence of carbon addition was not obvious and the highest iron recovery ratio reaches some 95.5% when the dephosphorization ratio was 37.68%. A high iron recovery ratio and a reasonable dephosphorization rate were incompatible under the conditions investigated in this study due to the reduced iron and because unreduced P-contained gangues were not efficiently separated. This method may provide a reference for the future utilisation of high-phosphorus iron ore.IntroductionWith the rapid growth of crude steel production in China, the source of iron ore tends to become increasingly strained and is facing the risks of raw material shortage for the iron and steel industry. In order to decrease the production cost, China has to focus on the utilization of its domestic low grade iron ores for the iron and steel plants [1-2]. China has a large deposit of high phosphorous iron ore with a reserve of 7.45 billion tons which is unused in any large scale [3]. Therefore, the development of a successful and economically viable technology for high phosphorus iron ore is of profound importance. To remove phosphorus from the high phosphorus iron ore, several mineral and metallurgical processes have been proposed, such as bio-leaching [4], roasting reduction plus melting separation [5], pre-reduction and screening methods combined with mechanical crushing or air jet milling[6] selective agglomeration plus reverse flotation [7]. However these processes are not cost effective or are time consuming. The traditional pyrometallurgical process( BF+ BOF) refuse this kind of ore mainly because that molten iron is saturated with carbon or high carbon content and thus all phosphor us in the burden goes to the molten iron[8]. Therefore, it is important to exploit the cheap and abundant high phosphorus iron ore as a resource in ironmaking. In recent years, the microwave was widely introduced as a heat resource for extractive metallurgy of iron ore or other minerals. For example, microwave assisted ore milling, microwave assisted carbothermic reduction of metal oxides and microwave assisted mineral leaching issues[9-10]"

Jan 1, 2014

By John G. Reid

When the paper "Operations at the Greenvale Nickel Project Mine and Refinery" was delivered at the 1st International Laterite Symposium in February 1979, the Yabulu Caron plant had been operating for four years and production had just stabilized. The design had been based closely on the Caron plant at Nicaro, Cuba, built in 1944, also by Freeport. Yabulu had 10 Herreshoff ore roasters and production in 1978 was 18,682 tonne nickel as impure oxide sinter and 763 tonne cobalt in a mixed sulphide with a cobalt to nickel ratio of 1 :2.5. In the 25 years since the 1st Symposium, two more roasters have been added, but dry ore processing rate has remained relatively unchanged at 2.4M Uyr to allow a lower feed rate per roaster with associated higher recovery. The ore source has changed from the domestic Greenvale mine to imports from New Caledonia, Indonesia and the Philippines. Nickel production between 1978 and 2003 has risen by 67%, cobalt has risen by 146% and the products have changed to high purity nickel compacts and "ChemGrade" cobalt salt. The plant changes that have contributed to the increased recovery, production and product value are discussed. Keywords: Caron, Yabulu, nickel, cobalt, ammonia

Jan 1, 2004

By James R. Craig

The General Image Processing System (GIPSY) is being employed for the quantitative textural analysis of complex sulfide ores from the Southern and Central Appalachians and for the determination of liberation characteristics of the mineral constituents during grinding. Optical images from a microscope-mounted TV camera or from 35mm film are converted into digital images which are subsequently analyzed by GIPSY, a transportable image processing software package. Properties measured by GIPSY include spatial distribution of mineral constituents, grain sizes, grain shapes, grain orientation and mineral co-occurrences.

Jan 1, 1982

By Guiming Yang, Xiaoxian Huang, Zhiyun Ji, Min Gan, Lishun Yuan, Xiaohui Fan, Zhiyuan Yu

"The roasting characteristics of hematite pellets containing MgO were studied where magnesia powder, serpentine and magnesite were used as magnesium-additives respectively. The mechanical strength of both preheated and roasted pellets decreased when MgO content increased, which implied the addition of MgO had an adverse effect on pellet consolidation. By adding flux containing CaO, the mechanical strength of both preheated and roasted pellets were improved. The addition of calcium flux facilitated the formation of calcium ferrite and provided a certain amount of liquid phase, resulting in faster diffusion ofMg2+ and Fe3+. The result showed that diffusing speed of Mg2+ was enhanced by 1.48 times, and rate constant of Fe203 crystalline growth was enhanced by 62% when basicity was around 0.4. Improvement of mineralization degree and recrystallization of Fe203 assisted in consolidation of hematite pellets containing MgO.IntroductionOxidized pellets are ideal iron-bearing burdens in blast furnace. At present, magnetite is the main raw material for oxidized pellet production in China. However, as the rapid development of iron and steel industry, resources of magnetite have been depleted and cannot satisfy the requirement of pellet production. Using hematite concentrates to produce oxidized pellets has become a trend [1, 2]. Many pellet enterprises abroad nowadays have adopted high proportions of hematite concentrates when producing oxidized pellets, e.g. the percentage is 100% in a lot of Brazilian factories [3, 4]. But high proportion of hematite concentrates will lead to low mechanical strength and high reduction swelling index of pellets. Some studies show that Mg-bearing pellets have excellent metallurgical properties, and the reduction swelling phenomenon can be solved by adding fluxes containing MgO [5, 7]. However, there are problems such as low pellet strength and bad roasting characteristics for MgO-bearing pellets, which remains an obstacle in pellet industry. Hence, it's vital to undertake the study on strengthening measures for indurations of Mg-bearing hematite pellets."

Jan 1, 2013

By Joseph Bloch

The hydriding of bulk metals and alloys is a gas-solid reaction in which a hydride product layer is initially nucleated adjacent to the gas-solid interface and continues to grow until a complete transformation of the parent (a) phase into the hydride phase. The combination of measurements of the overall hydriding kinetics of samples having defined shapes and dimensions, together with examinations of partially hydrided samples, enables the presentation of the reaction rate in terms of an appropriate reaction model. A common and important type of topochemical development of the hydride in bulk metals and alloys involves a hydride layer formed on the metallic surface. The continuity of the layer can affect the reaction rate. The rate of hydrogen absorption in a sample, in the presence of a hydride layer, is usually analyzed using a model combining several sequential steps in which the hydrogen is transferred from the gas phase into the reaction site. Coupling the flux equations across the layer under proper steady state conditions, results in a complex rate equation in which the steady state rate of hydrogen absorption (proportional to the hydride layer velocity) is expressed in terms of the pressure, temperature, the rate constants of the sequential steps and the critical concentrations of hydrogen in the hydride. Generally, the rate constants of the individual microscopic processes are comparable in magnitude, so that the overall rate is not controlled by any of the specific sequential steps. However, there are two limit cases related to the first stage, the adsorption, for which the general rate equation is much simpler, namely, the fast and the slow adsorption approximations. Using this limit cases, equations are derived for the steady state hydriding rate of a given system. These equations provide means to anticipate the pressure dependence of the steady state absorption rate under low pressures, close to Peq and under very high pressures. At the low pressure regime both the fast and slow absorption cases yield linear pressure dependence. For the very high pressure range, it is found that the rate become independent of the applied pressure. The rate is given then by a combination of the individual rate constants of the system and the critical hydrogen concentrations. The model is shown to apply in several real cases, such as ZrCo, LaNi5 and titanium.

Jan 1, 2002

By Kimio Itagaki

The distribution behaviours of the VA elements between the gas, slag and matte phases in copper smelting were evaluated on the basis of the thermodynamic data, most of which were determined by the authors. The distribution is basically dependent on the process factors such as temperature, the content of the element in charge, the amount of the waste gas and degree of vapour saturation with the elements. The thermodynamic quantities such as the activity coefficients of the VA elements in matte, the activities of iron and copper, SO2 or 02 potential and the distribution ratio of the elements between the slag and matte phases seriously affect the distribution, and the behaviours in various smelters could be explained systematically and reasonably by considering the changes in these quantities, In oxidation smelting at PSO2= 0.1 to 1 atm, the proportion of arsenic and bismuth in gas is predomi22t for the arsenic and bismuth distributions in both smelting and converting stages. The degree of vapour saturation has serious effect on the distribution, and sufficient contact between gas and matte phases is desirable for transferring arsenic and bismuth into gas phase.The elimination of antimony by means of vaporization is not significant. In reduction smelting at po2 = 10-11 atm, the proportions of arsenic and antimony in the gas phase are quite small, but the proportion of bismuth does not change significantly.

Jan 1, 1983

By Ailton S. Ferreira, Rubén J. Sanchez Rodriguez, Sergio N. Monteiro, Felipe Perissé D. Lopes, Teresa E. Castillo

"Polyester composites reinforced with natural lignocellulosic fibers have, in recent times, been gaining attention in engineering areas as lighter and cheaper alternatives for traditional composites such as the ""fiberglass"". One of the strongest, the curaua fiber, is today being considered as reinforcement of composites for automobile interior parts. In fact, several research works are currently being dedicated to curaua fiber composites since physical and mechanical properties are required for practical uses. In this work, the thermal behavior of polyester composites reinforced with up to 30 % in volume of curaua fibers was investigated by differential scanning calorimetry, DSC. The results showed endothermic and exothermic events associated with water release and possible molecular chain amorphous transformation. Comparison with similar composites permitted to propose mechanism that explains this DSC thermal behavior.IntroductionThe modem composite materials, especially those reinforced with synthetic fibers such as glass and carbon, have been used since last century to attend the demands required by most technological fields, from home appliances to aerospace [1]. In fact, fiber composites offer significant advantages over monolitic materials, such as common metallic alloys, plastic and ceramics. One of the most important is the ratio between the ultimate stress and the density, known as the specific strength. For example, in common glass fiber polymer composites, the so called ""fiberglass'', the specific strength of around 400 MPa.cm3/g is higher than any conventional monolitic material. However, drawbacks exist. The energy required to fabricate ""fiberglass"" generates large emissions of C02, which are responsible for global warming. Moreover, ""fiberglass"" is not recyclable and cannot be incinerated [2]. As a result, most synthetic fiber composites end up in landfills or contribute to rivers and oceans pollution."

Jan 1, 2011

By Li Ma, Shaoguo Chen, Gele Qing, Qihang Liu, Keng Wu

Olivine contains higher MgO element, which can be added into blast furnace burden to improve slag stability and fluidity. Effect of calcined olivine and untreated olivine on low silicon pellet production process and quality was studied in this paper. The results shows, calcined olivine has no effect on bursting temperature of green pellet, however the bursting temperature of green pellet will decrease with increase of untreated olivine ratio. Untreated olivine has slight effect on green pellet strength than calcined olivine while the ratio is higher than 2%. The compressive strength of low silicon pellet will increase first and decrease afterwards with increases of calcined olivine ratio under firing temperature of 1250°C, whereas, the changing sequence is reverse fired under 1280°C. The result of untreated olivine pellet compressive strength is same as calcined olivine pellet. However, the compressive strength and metallurgical property of calcined olivine pellet is slightly higher than that of untreated olivine pellet under same condition.

Jan 1, 2015

By Jayagopal Ucbil, M. Krishna, V. T. Vijayalakshmi

"The pitting susceptibility of aluminium metal matrix composites reinforced with garnet particles has been examined using static weight loss method by exposing the metal matrix composites (MMC) specimens to the action of IN HCI acid at laboratory temperature for different time intervals. It was found that the corrosion rate decreased with increase in weight percentage of reinforcement while the corrosion rate was a function of the matrix alloy but not of the reinforcement material. Further, it was found that the rate of corrosion was dependent on the interface region formed between the reinforcement and the matrix. A comparison of the base matrix with the corresponding composite when subjected to heat treatment for varying periods of 4, 8, and 12 hours respectively was made. The comparison revealed that corrosion resistance of the composite increased with the duration of heat treatment and this has established a considerable improvement in corrosion resistance of the composite when compared with the base matrix.IntroductionMetal matrix composites (MMCs) offer designers many added benefits, as they are particularly suited for applications requiring good strength at high temperature, good structural rigidity, dimensional stability, and light weight [1-5]. The trend is towards safe usage of the MMC parts in the automobile engine, which work particularly at high temperature and pressure environments [6-7]. Particles reinforced MMCs have been most popular over the last two decades. Among the MMCs, the most popular families are represented by aluminium reinforced with ceramic particles. Although the incorporation of the second phase into a matrix material can enhance the physical and mechanical properties of the base metal, it could also significantly change the corrosion behavior."

Jan 1, 2000

By Atinuke Oladoye, David Esezobor

"Particulate Copper Silicon carbide (Cu-SiCp) composites find application as wear and heat resistant materials in electrical sliding contacts such as in homopolar machines, railway overhead current collector systems where high electrical/thermal conductivity combined with good wear properties is required. However, challenges occur during machining due to the presence of hard reinforcement in the matrix. This may lead to high turnover of tool wear and poor surface finish. The adoption of near-net shape technology to produce such hard-to-machine metal matrix composites and subsequent finish machining with its attendant cost has reported limited success. This paper critically appraises the challenges and opportunities in the improvement of tribological characteristics of particulate Cu-SiC composites and identifies low cost reinforcement material that could be used to improve its tribological characteristics.IntroductionTribology consideration is increasingly becoming a decisive factor in the design and selection of materials for applications involving interacting surfaces in relative motion. The consideration is mainly on the combined effects of friction and lubrication on material's wear integrity and performance amongst other. Annual losses due to tribology in the US industries are estimated at between 1-2% of the Gross National Income [1], in Russia it is about 1-4% of the GDP [2]. Thus, the attributes of tribology has become imperative in modem machinery especially those applications involving sliding and rolling surfaces, and electrical contacts [3- 8].These are readily found in homopolar machines, internal combustion engines, aircraft engines, gears, cams, seals and railway overhead current collector systems [9-12]. In these systems, the dissipation of frictional heat arising from the interacting surfaces as quickly as possible imposes constraints on the choice of materials for such application to prevent softening, plastic and shear flow and the transfer of metal as wear debris onto the interacting surfaces. If these possibilities occur, system performance is compromised and premature failure may result. Materials for these systems are expected to possess high electrical and thermal conductivities, low coefficient of thermal expansion, good corrosion resistance and high melting point [3-8, 13]."

Jan 1, 2011

By Jenq-Gong Duh, Jyh-Wei Lee

"Hard chromizing process is a method for developing a surface modified coating providing wear, corrosion resistance and high temperature surface protection. Two carbon steels with 0.45 wt% and 0.95 wt% carbon contents, respectively, were chromized with pack cementation process at 950'C for 4 and 9 hours, respectively. The phase transformation and microstructure phenomena of chromized coating layer and matrix of two steels were studied with X-ray diffractometer and electron probe microanalyzer. (Cr,Fe)23C6 and (Cr,Fe)7C3 carbides and (Cr,Fe)2N1-x nitride phases were observed on the chromized surfaces. The thickness of chromized layers obeyed the parabolic rate law. The mechanism and diffusional kinetics of the chromizing process were proposed. The diffusivity of chromium in the (Cr,Fe)7C3 carbide phase was calculated using the moving boundary method.IntroductionChromizing process is one of the surface treatment technologies that can produce a chromium contained surface layer with sufficient corrosion and wear resistance on the steel matrix [1-7]. The relatively low cost and no ""line-of-sight"" restrictions are main advantages of chromizing. Adequate bonding strength of these coatings to the substrate was reported [7]. Chromizing process can be classified into soft chromizing and hard chromizing [2]. Soft chromizing is applied to steels containing less than 0.1wt% carbon through which chromium will be diffused. High temperature oxidation resistance improvement is the main purpose of soft chromizing process. On the contrary, the hard chromizing can be applied to steel containing more than 0.3wt% carbon, and very hard chromium nitride and carbide layers will be formed on the surface, which are very resistant to wear, corrosion and temperature [5-7]. In the previous studies on the Fe-Mn-Al-Cr alloy [5,7] and carbon steels [6], the thickness (X) of chromizing layers was analyzed and found the parabolic rate Jaw prevailed:"

Jan 1, 2004

By Kenshi Kawabata, Mitsuji Ueda, Junko Umeda, Katsuyoshi Kondoh, Kantarou Kaneko

Solid-state recycling process of in-house scraps of machined magnesium (Mg) alloy wastes has been established to directly produce wrought materials via the repetitively plastic deformation by Roll-compaction (RCP) and the conventional hot extrusion. The coarse chips, wasted in machining AMX602 (Mg-6Al-0.2Mn-2Ca) cast billets used for the gate bar used in Electronic Toll Collection (ETC) of the high-way system, were employed as the input materials in this study. RCP process enabled to serve coarse Mg alloy powder consisting of refined grains and intermetallics with no re-melting. They were easily consolidated by hot extrusion, and their wrought alloys showed both homogeneously refined grains less than 1~2 µm by dynamic recrystallization and randomized texture by repetitive plastic deformation on the input wastes. These materials revealed extremely advanced mechanical properties of high tensile strength of 356MPa and high ductility of 14.8%, compared to the originally virgin materials with 270MPa TS and 5% elongation. When applying the same Mg alloy wastes via RCP process to the mass production in the company, the large-scale extruded materials also indicated the superior tensile properties. It means that this direct solid-state process is held as “Up-grade recycle of metal wastes”.

Jan 1, 2008

By Gustavo Díaz, Miguel A. García, Carlos Frías

"Under the auspices of the Commission of the European Union, a consortium composed of six European organi~ations has conducted a project to scale up the PLACID electrowinning cell to industrial size within the Placid process development. This paper is concerning the results and achievement of the industrial cell prototype after more than 1,000 hours operating time and about 10,000 Kg electrolytic lead production. In general, results have been very satisfactory, demonstrating the ability ofthe PLACID electrowinning cell to produce top quality electrolytic lead (> 99.99 %) with high current efficiency and low energy consumption.IntroductionThis paper is concerning the development of an industrial size PLACID electrowinning cell within the PLACID process development. This project began on January 1993 and was finished on April 1996.Lead metal production and manufacturing industries produce large amounts of dusts and also lead bearing slags. Spent lead-acid battery recycling also produces lead oxides from the battery pastes rather similar to those mentioned above. Those lead secondary materials are hazardous and difficult to handle by usual procedures.Existing processes to treat-lead oxides may inflict considerable damage on the environment, incur high operating costs and have limitations to produce top quality lead.The main aim of this project has been to develop a novel hydrometallurgical process able to deal with different lead bearing materials, mainly lead oxide secondaries: lead-acid battery pastes, lead fumes, furnace slags, oxide residues, etc., producing ""four nines"" pure lead in an efficient manner with a benign influence on the environment; it is called the PLACID process."

Jan 1, 1997

By R. Harris

Blister copper melts of 800 g to 1000 g containing less than 1 wt % S and up to 3 wt % Ni were desulfurized at 1523 K in air or by a pure oxygen jet blown at 75,500 and 1000 cm3/min, from 1 cm above the melt. Rates of desulfurization and oxygen pickup were measured and visible surface phenomena were photographed and videotaped. It was observed that SO2 was evolved from Cu-S melts in a manner reminiscent of the effervescence seen in carbonated drinks. The effervescence lasted up to 20 minutes and resulted in the ejection of material up to a height 50 cm above the melt surface. Sporadic discharge of large bubbles was also observed in a Ni containing melt top-blown with oxygen at 1000 cm3/min. The Cu-S melts top-blown with oxygen experienced faster sulfur elimination as compared to stagnant melts exposed to air and experienced only a single period of turbulent SO2 evolution, which occurred almost immediately after oxygen injection commenced. The Cu-S melts exposed to air experienced multiple episodes of effervescence. The stagnant blister copper melt containing nickel did not exhibit effervescent behaviour and experienced a lower rate of sulfur elimination compared to Cu-S melts tested under similar conditions. The present article examines the role of surface phenomena in determining the observed behaviour.

Jan 1, 1999