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By P. Klut, D. Groult, R. Marechalle, B. T. H. Bonnema

In the past 5 years, Compagnie Europeenne de Dezingage (CED) has developed a successful dezincing process and the St. Saulve pilot plant has evolved into a commercially successful production plant. Currently the plant meets all the required standards for scrap and zinc quality, output capacity, availability, and meets the prescribed environmental emissions standards. The initial process problems relating to zinc recovery, uncontrollable explosions and sodium hydroxide aerosol emissions have all been solved. Presntly, the yearly production of dezinced scrap is around 50.000 tonnes/year; this capacity is enough to supply the local market. This capacity can be increased easily to 65.000 tonnes/year or more. The market for dezinced material is growing due to the increased consumption of galvanized material on one hand and on the other hand the higher demand for high quality scrap. The proven technology of CED is currently patented worldwide, but CED is inviting licensees to implement the dezincing technology in other parts of the world.

Jan 1, 2000

By Jyri Talja, Shaolong Chen, Hannu Mansikkaviita

"Drying (water removal) prior to smelting is always economically feasible. Unnecessary heating of vapour can thus be eliminated resulting in savings of5-15 MUSD every year.Thermodynamically removal of one ton of water out of copper concentrate at 100 °C (with 10 % moisture) requires approximately 3150 MJ/tH2o, consisting of heating of the water (377 MJ), heating of the concentrate (509 MJ) and water evaporation (2260 MJ). This is quite independent of the selected drying technology. In reality some more heat is needed as higher temperature is practiced to enhance the drying performance and to reduce the equipment size.Major nominator in drying energy efficiency is amount of gases, which depends greatly on the drying technology. Dryers based on direct heating with fossil fuels have high gas flow rates, and thus they require additional energy of about 1400-1600 MJ/tH2o, compared to indirect modemsteam drying at 250-400 MJ/tH2o.Significant benefits in energy consumption (900-1300 MJ/tH2o) with additional potential for a bonus profit of 2-4 MUSD/y year, together with full elimination of some 40 000 tpy CO2 per mid-size dryer is available by selecting sustainable, energy efficient steam drying.IntroductionRemoval of water from the concentrate is very energy intensive thus having a significant environmental impact. However, drying prior to smelting is always economically feasible and very often viable also from the perspective of process operations. This environmental impact of drying can, however, be decreased or even fully eliminated with proper selection of the drying technology.Energy incorporated in drying consists always of a number of phases like liquid (water), solids (concentrate) and gases (water vapour, purging I dilution air, combustion gases). Each phase is heated to a specific temperature during the drying process.Heating of water, heating of the concentrate and water evaporation consumes more or less the same amount of energy despite of the drying technology (3150 MJ per ton of water). In conventional drying this amount of energy is achieved by combustion of fossil fuels wirg subsequent CO2 emission. Alternatively, chemical energy derived from sulphide smelting can be utilized in a form of steam thus generating zero emission ofCO2, in modem steam drying."

Jan 1, 2012

By Marisa Di Sabatino, Michael Phan Knudson, Mari Juel, Eivind Øvrelid

"A p-type Czochralski silicon ingot doped with boron was characterized for resistivity, minority carrier lifetime, interstitial oxygen, and metallic impurities. Analyses show a peak in resistivity and a dip in lifetime both occur 5 cm from the top of the ingot crown. This peak in resistivity deviates from the expected trend based on Scheil's equation for boron distribution. High concentration of interstitial oxygen in this area suggests that other oxygen-related defects, such as thermal donors and precipitates, may also be present here, and the observed peak in resistivity and dip in lifetime could be attributed to such defects. The low lifetime of 15-30 µs at minority carrier density of 7.5 x 1014 cm-3 is likely due to copper contamination.IntroductionSolar energy resources vastly exceed all other alternative energy resources, ensuring that solar power must play a crucial role in the evolving energy market. The economic viability of solar power in competition with other energy resources depends upon finding efficient, cost-effective, reliable, and controlled methods for solar cell production. In this regard, minimizing waste (such as material with unsuitable electrical properties that hinder solar cell performance) is a vital component of making solar cell manufacturing cost-effective. Impurities affect electrical properties of solar cell silicon in different ways (i.e. [1, 2, 3, 4, 5, 6]). In this work we focus on the role of oxygen and metallic impurities. Understanding oxygen impurities in silicon is critical to solar cell development because oxygen has been attributed with influencing critical electrical properties including resistivity and minority carrier lifetime and thereby potentially hindering solar cell performance or rendering material unsuitable for solar cells.[1, 2] Furthermore, oxygen is a common impurity in the standard type of solar cell silicon, Czochralski (CZ) silicon, due to diffusion of oxygen from the silica crucible into the melt during crystallization. [7] This study investigates the effects oxygen impurities have on the electrical properties of p-type CZ silicon."

Jan 1, 2013

By B. L. Chulu

In the carbothermic reduction of lead sulfate to produce lead, the inclusion of soda ash (Na,CO,) in the charge provides for the control of sulfur dioxide in the effluent gas. An important mechanism in the process appears to be the carbothermic reduction of the sodium carbonate whereby sodium gas and carbon monoxide are produced. These intermediates then participate in the reduction of the lead sulfate to produce lead metal and stable sulfur species in the molten slag phase. In addition, there is some evidence that the presence of lead metal in the charge may also serve to increase the lead recovery in the process. These aspects were investigated by conducting laboratory-scale smelting tests with small charges (;3g), at 1173°K(9000C). Recovery did not exceed 74w% and the role of incipient lead metal in the charge could not be clearly assessed.

Jan 1, 1993

By Yang Guangqing, Shao Jiugang, Zhang Jianliang, Wan Dan, Fu Yuandi, Guo Hongwei

"Resource of metallurgical coke is becoming scarce, and although coke can be partially replaced by pulverized coal injection, there are many restrictions for further increase in coal ratio. Mixed charge of ore and lump coal from top to replace more coke was studied in this paper. Softening-melting property of the burden was affected by charge of lump coal. Softening-melting properties of mixed charge of ore and coke, mixed charge of ore and lump coal were tested respectively. Results show: the property of the burden mixed with coke is superior to the burden mixed with lump coal; lump coal would not deteriorate softening-melting property of the burden and some of them can even improve softening-melting property of the burden. Top charge of lump coal would not deteriorate softening-melting process, and this should be a new way to increase coal consumption to decrease coke rate.IntroductionThe blast furnace is still the predominant process for the reduction of iron ore and will probably remain so for the next decades. Metallurgical coke is becoming scarce and expensive, so the cost of hot metal can be decreased by reducing the consumption of metallurgical coke[l]. Coke can be partially replaced by pulverized coal injection, currently the highest rate of pulverized coal reached 266kg/tHM, most of blast furnace PCR is about 150kg/tHM, and it is very difficult to further increase of PCR. Nut coke is charged into blast furnace mixed with iron ore, not only for improving utilization of metallurgical coke, but also for lowering the coke rate. Presently the majority of blast furnaces in the world use nut coke although its amount is very different: from 10-20 to 70--100 kg/tHM and more[2-4].The effect ofnut coke in blast furnace is extensively researched, and the main conclusions recommend: to improve gas permeability of cohesive layer in blast furnace, to promote reduction of iron burden, protect metallurgical coke from the solution in the shaft due to higher reactivity of nut coke. There is no special requirement for the strength of nut coke[5-8]. Nut coke is also used for sintering fuel, which may lead to the shortage of the nut coke charging into blast furnace. So lump coal mixed with iron ore is considered to be charged into the blast furnace, not only to reduce the cost of grinding coal, but also to increase the use amount of coal."

Jan 1, 2013

By Jian-hua Ren, Guang-liang Wu

A lot of dust is produced in iron and steel enterprises, giving rise to serious environment pollution, with which all countries are trying to find methods to deal. The influence of relevant technological factors on dephosphorization was investigated in laboratory, and the effect laws of that were analyzed. The results demonstrate that, in the given conditions of the best slag-metal proportion for hot metal dephosphorization is 1:10, and the optimum temperature is 1350 , The phosphorus distribution ratio of dephosphorization agent containing converter dust of 30% has the maximal value, with dephosphorization rate reaching 85%. Under the optimal conditions, premelting dephosphorization agent can significantly improve the ability of dephosphorization, dephosphorization efficiency increasing to 92%. Therefore, the dust can substitute the oxidant and fixative of dephosphorization agent, be used in hot metal dephosphorization, to enhance the efficiency of utilization.

Jan 1, 2016

By Hiroyuki Matsuura, Fumitaka Tsukihashi

"Emission of CO2 gas from steelmaking industry covers more than 12 % of total CO2 emission in Japan. Though many efforts have been made to curtail energy consumption and high energy efficiency of Japanese steel production process has been achieved so far, further reduction of CO2 emission is strongly requested to develop sustainable steel production process and produce “green material”. Recently, authors have proposed the innovative hydrogen production process, in which water vapor is reacted with discharged steelmaking slag to produce hydrogen gas. This reaction can be achieved without any external energy source and operated by huge thermal energy associated with steelmaking slag and FeO or unrecovered Fe droplets that are relatively rich in the slag. In this paper, thermodynamic calculation results with various initial conditions in terms of hydrogen productivity were presented. Laboratory-scale experiments were also conducted to clarify the validity of thermodynamic calculation and the reaction rate in realistic conditions.IntroductionIronmaking and steelmaking process from iron ore through blast furnace and BOF is an essential steel production route for Japanese steel industries to supply high quality steel products in large quantity to society stably. Blast furnace – BOF process requires huge amount of fossil fuels such as mainly coal, resulting the emission of considerable amount of CO2 gas. Since the emission of CO2 gas from steel industries, about 147 Mt (FY2011), accounts for approximately 12 % of domestic CO2 gas emission in Japan (FY2011),[1] it is an urgent issue for steel industries to develop environmental-friendly ironmaking and steelmaking process and reduce CO2 emission. Various kinds of gases and by-products generated from ironmaking and steelmaking processes have been recycled as much as possible at present. Enormous thermal energy is also generated from processes and released to surrounding atmosphere as various forms such as sensible heats of gases, molten steels or by-products, and as heat losses. However, these energies are not utilized before final dissipation to atmosphere. Although various technologies to utilize thermal energy from ironmaking and steelmaking processes have been attempted to develop, practical application of these technologies has not been achieved because the thermal energy is not always useful as an energy source. In steelmaking process by BOF, fluxing agent such as CaO is added during reefing and thus about 100 kg/t-steel of steelmaking slag are generated. Since the steelmaking slag is discharged at temperature range between 1873 and 1923 K after discharge of refined molten steel, it also has large thermal energy. Amount of generated BOF slag is 11.0 Mt/y (FY2012) in Japan.[2] Assuming the amount of steelmaking slag is 10 Mt/y and its average heat capacity from room temperature to 1923 K is 1 kJ/kg·K,[3] unutilized heat is estimated to be 16 PJ/y, which is equal to annual energy consumption of 420 thousand families in Japan.[4]"

Jan 1, 2014

By Orlando C. Rojas

The Potrerillos Smelter commissioned a new El Teniente converter in 1985. As a result of the use of this technology, the Peirce-Smith converters have been processing only high grade matte or white metal. These operational changes resulted in damages to the converter shells, excessive splashing and cold dope generation and very short refractory campaigns. The paper shows the modifications to the tuyere angle, mouth design changes and new techniques for mouth cleaning and gas handling. Operational results up to 1991 are also shown.

Jan 1, 1993

By Mariana Barcelos, Frederico Muylaert Margem, Giulio Rodrigues Altoé, Pedro Amoy Netto, André Gomes, Sergio Neves Monteiro

Environmentally correct composites, made from natural fibers, are among the most investigated and applied today. In this paper, we investigate the mechanical behavior of polyester matrix composites reinforced with continuous fique fibers, through bending tensile tests. Specimens containing 0, 10, 20 and 30% in volume of fique fiber were aligned along the entire length of a mold to create plates of these composites, those plates were cut following the ASTM standard to obtained bending tests specimens. The test was conducted in a Instron Machine and the fractured specimens were analyzed by SEM, the results showed the increase in the materials tensile properties with the increase of fiber amount.

Jan 1, 2015

By Marcio Toshio Tanaka, Marcelo Breda Mourao, Cyro Takano, Cesar Yuji Narita

"The concerns in questions related to the environmental impact in the steelmaking industries caused mainly on the gas emissions such as the dioxide carbon are due to its raw material such as the coal, a fossil and non renewable resource. The purpose of this paper is to replace from 10% to 50% of the coal used in cokemaking by mixing it with a renewable source (wood charcoal). The powder (- 325 mesh) from both raw materials (coal and wood charcoal) were mixed in order to obtain a briquette that was then heat treated at 1100°C to obtain the biocoke. Results of usual analysis (coke reactivity index, coke strength after reaction and cold crushing strength test) were employed to compare to regular coke briquettes. It was found that biocoke with different amounts of wood charcoal present features enabling it to be used in some ore reductionprocesses.1. IntroductionThe iron and steelmaking industry is a heavy emitter of carbon dioxide; according to the World Steel Association, 6.5% of global emissions of this greenhouse gas is due to the production of ferrous materials [ 1]. This is due to the fact that the fuel and reductant employed in the blast furnace is metallurgical coke, obtained from fossil coal. There are some projects aiming to reduce or even eliminate the emission of fossil GHG in the iron and steelmaking process [2]. Most of them propose the capture and storage of the gas (CCS) [3], a technology not yet proven. Other studies point out that the coke consumption in the blast furnace could be reduced by using high reactivity coke; this could lead to lower temperatures in the thermal reserve zone of the blast furnace and consequently less fuel rate in the furnace.The use of biomass in the iron ore reduction process is known as an environmentally accepted solution, as biomass does not release already fossilized carbon."

Jan 1, 2013

By J. Pérez

A lead smelter slag with high copper, lead, arsenic and silver contents was treated at laboratory scale for arsenic removal. The slag was first leached at atmospberic pressure with sulfuric acid and oxygen. According to arsenic contents leaching of most of the arsenic was achieved in either one or two stages, producing a lead-silver rich residue and a solution high in copper and arsenic concentrations. Alternative routes were considered to treat the resulting solution. Firstly, solvent extraction of arsenic with a mixture of TBP and 2-etbyl-bexanol was tested and extractions of over 95 percent of arsenic were achieved. Secondly, a copper arsenate precipitation treatment was done to eliminate arsenic and copper from solution.

Jan 1, 1996

By J. S. Kirkaldy

A theoretical procedure is demonstrated for calculating two-dimensional binary cellular single-valued interfaces and extended to triple-valued (remelt) shapes. The numerical calculations for the single-valued local equilibrium problem which yield unique shapes as functions of the supersaturation parameter a and the partition coefficient k are reviewed. The cell amplitude L and wavelength A scale identically as the inverse velocity to the 112 power and the aspect ratio r is a constant equal to 312, independently of a and k for a < 0.5.. For 0.5 < a < m, L, A and r decrease asymptotically to zero indicating the finite amplitude nature of the instability at a = 1 and the existence of sub-marginal states which converge to a flat interface at a- m (Glv- m). Scaling comparisons between equilibrium single-valued and triple-valued and deep-rooted non- equilibrium cells are made.

Jan 1, 1992

By C. M. Wai

"Metal species in solid and liquid materials can be extracted by supercritical carbon dioxide containing a suitable ligand. This in situ che1ation-supercritical fluid extraction technique offers several advantages over conventional solvent extraction including minimization of organic liquid waste generation and exposure of personnel to organic vapors. One unique feature of this technique is that metal species can be removed from solid materials directly using supercritical carbon dioxide as a solvent. Several ligand systems including dithiocarbamates, B-diketones, organophosphorus reagents, and macrocyclic compounds have been tested for metal extraction in supercritical carbon dioxide. This novel extraction technique may have important applications for metal recovery and mineral processing.IntroductionSupercritical fluid extraction (SFE) offers several advantages over conventional solvent extraction including the minimization of organic liquid waste generation and exposure of personnel to organic vapors.[1] The high diffusivity, low viscosity, and T-P dependence of solvent strength are some attractive properties which make supercritical fluids excellent candidates for extraction and recovery of organic compounds from solid materials [2] Carbon dioxide is a gas of choice for SFE because of its moderate critical constants (Tc = 31 °·C and Pc = 73 atm), inertness, and availability in purified form. After extraction, the fluid phase is depressurized to separate organic solutes from CO2 gas and the gas can be recycled for repeated use. The SFE technology has been applied to industrial scale operations such as the preparation of decaffeinated coffee and hop extracts."

Jan 1, 1996

By Samantha Moodley, Rauf Hurman Eric, Cevat Kucukkaragoz, Aditya Kale

"Two titania slags, rutile and synthetic rutile were chlorinated with petroleum coke and CO in a small bubbling fluidized bed reactor. The study aims to identify differences in chlorination mechanism, compare conversion rates, blowover and the chlorination of impurities for the various titania feedstocks at different temperatures.Chlorination rates were highest at 1000ºC; rutile chlorination significantly increases as temperature increases from 800ºC to 1000ºC. At 1000ºC, synthetic rutile had the highest chlorination conversion rate; this was followed by Slag B which in turn was more reactive than Slag A and rutile. The mechanism for slag, synthetic rutile (SR) and rutile chlorination differs. Synthetic rutile feed is porous, providing a larger surface area for the chlorination reaction, hence the highest conversion rates was attained. Titania slag becomes porous with the initial chlorination of FeO and MnO whilst rutile remains solid. As the porosity of slag particles increases so does its tendency to be elutriated. Ti2O3 is oxidized within the early stages of chlorination during the chlorination of FeO and MnO. Ti2O3 not oxidized is then rapidly chlorinated.IntroductionTitanium dioxide (TiO2) is the most common compound of titanium, about 95 - 98% of extracted titanium minerals is processed into TiO2 white pigment [1]. Two processing routes exist for the production of TiO2 pigments, i.e., sulphate and chloride based processes. In the chloride process, titania feedstock is fed to a fluidized bed reactor together with reductant and chlorine gas. A temperature of 1000 - 1300ºC is maintained in the reaction zone and apart from silica, zirconia, uranium and thorium, virtually all the metal oxides in the feed are converted to their respective chlorides [2]. Chlorine is recovered and recycled back to the reactor."

Jan 1, 2012

By John E. Litz

The Denver Process is a chemical/metallurgical process for treating radioactive or mixed wastes by extraction and concentration of the radioactive and/or hazardous component(s). The process was developed at bench scale, evaluated at pilot scale, and will be implemented at full scale to remediate a low-level radioactive sludge. Six unit operations comprise the process: feed handling, leaching, solvent extraction, electrodeposition, precipitation, and tailing preparation. Unit operation design may be modified to tailor the process for varying feed stock composition. Radioactive or mixed waste is reacted with aggressive reagents in an aqueous phase, solubilizing targeted components. These components are then selectively extracted and concentrated in subsequent steps. Waste solids and solution exit the process as non-hazardous non¬radioactive waste. Dehydration of aqueous waste by submerged combustion eliminates aqueous discharge.

Jan 1, 1994

By A. V. Tarasov

The proposed process is based on creating a controlled frothed layer of molten slag, in which fine particles of carbonaceous reductant and raw material to be processed are mixed with emulsified iron. Frothing of the slag layer without external blowing occurs as a result of intensive evolution of gaseous reduction products. The froth reaction process is maintained due to the heat of an electric arc in the slag layer. When the metal bath is heated by the arc to 1400- 1 500°C, the low temperature of the slag surface of about 1200-1 300°C is maintained due to low thermal conductivity of slag froth preventing heat loss. In order to maintain the required slag froth level and control the process temperature, air tuyeres are installed above the slag bath; blowing air serves also for oxidation of zinc in fumes and for its transportation. High adsorption and thermal insulating properties of slag froth ensure virtually complete elimination of dust and mist entrainment along with low heat losses. The main macrokinetic regularities of the carbon thermal reduction of zinc-containing slag melts have been studied under frothing conditions. The mechanism of formation of gas-slag emulsion has been identified under the conditions of reaction [C]+[O]=CO occurring locally at the slag-metal interface. It has been demonstrated that under the froth reduction conditions the zinc removal rate from the melt increases on the average by 3 to 5 times. Based on the physical and chemical data obtained, basic principles of the dezincing technology have been developed for different intermediate oxide iron-containing products produced in the process of ferrous and non-ferrous metals production.

Jan 1, 2002

By Rubén J. Sánchez Rodriguez, Carlos M. Fontes Vieira, Carlos E. Gomes Ribeiro

Ornamental compound stone are produced by industry for decades, however, few published studies describe these materials. Brazil has many deposits of stone wastes and a big potential to produce these materials. This work aims to evaluate the chemical resistance of ornamental compound stones produced with marble waste and unsaturated polyester. An adaptation of Annex H of ABNT NBR 13818:97 standard, with reagents commonly used in household products, was used. The results were compared with those obtained for natural stone used in composite production.

Jan 1, 2015

By David Dreisinger

The cyanidation of copper containing gold ores results in the co-dissolution of copper along with gold. Copper dissolution results in elevated cyanide consumption that may make the treatment of the gold ore uneconomic. Copper-cyanide species in gold mill effluents may increase the environmental toxicity of the gold mill solutions. The objective of this study was to examine the use of solvent extraction to recover the copper cyanide species from gold mill effluents. Solvent extraction with Cognis (formerly Henkel) reagents LIX 79 and LIX 7950 was studied. Excellent extraction of copper and cyanide was achieved using pH control in extraction. Copper and cyanide may be stripped from the reagents using basic eluants. Various routes for copper and cyanide recovery from the strip solution were studied. Excellent results were obtained using electrowinning in both divided (Nation membrane) and undivided cells. Cyanide recovery was obtained by AVR treatment of a bleed stream from electrowinning. Full results of solvent extraction, copper and cyanide recovery are reported.

Jan 1, 1998

By Yuzhe Zhang, Xiaodi Huang, Xinli Wang, Bowen Li, Matthew Andriese, Jiann-Yang Hwang, Zhiwei Peng, Likun Li

With the development of the world, the waste tires have been a serious environmental problem. There are about 2 billion waste tires produced all over the world every year and about 500 million waste tires are produced in the United States. Most of the waste tires are land filled, which waste a lot of space. It takes hundreds of years to resolve the macromolecules of waste tire into the standard which does not pollute the environment. Microwave irradiation is a thermal processing way for waste tires decomposition. In this study, the relative dielectric loss factor of the tire at various temperatures was determined to understand the behavior of tires under microwave heating.

Jan 1, 2016

By H. Itou, J. M. Toguri, T. Takasu

"Marangoni convection has a large effect on materials processing since it remarkably enhances heat and mass transport near a free interface. To have a better understanding of the behavior of Marangoni convection in molten salts, observation and calculation of the thermal convection in a column held between a pair of Pt disks (2mm in diameter) fixed to hot thermocouples, were carried out.Calculated flow patterns and absolute values of fluid velocity agreed well with the observed results. When the temperatures of both disks were set equal and the height of liquid column was 2.4mm, four vortexes were generated on the longitudinal plane with a typical velocity of 15mm/s . From the calculated isothermal lines, the behavior of the enhanced heat transport was obvious; fluid heated at the disks was conveyed to the free surface and the cooled fluid at the surface was conveyed to the inner region. Increase in the height of column and/or increase in the absolute value of applied temperature difference lead to increase in fluid velocity lineally in this calculation range.IntroductionIn the processing of many materials, fluid flow of melts has a large effect on refining capabilities and on the characteristics of the produced material. Marangoni convection is generated when a spatial gradient of interfacial tension exists on the free interface due to differences in temperature and/or concentration. This promotes heat and mass transfer locally near the interface.For example, Marangoni convection which are created following the dissolution of interfacially active materials, increases the local corrosion rate of refractories (1-3). In absorption and discharge of oxygen and/or nitrogen in a molten metal, the effective reaction rate of the gas components through the gas-liquid interface increases (4-7). Also in crystal growth, the distribution of defects and impurities in the crystal is affected and this can alter its quality (8-11 ). The temperature distribution is also affected and can greatly change the productivity. For these reasons, the effectiveness of Marangoni convection in refining should be quantitatively clarified and its control should be better understood."

Jan 1, 1997