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By Alan DonaldsoN

Plasma Quench production of titanium is the thermal dissociation of titanium tetrachloride into gaseous titanium and chlorine followed by rapid quenching to prevent back reactions. Titanium tetrachloride dissociates into titanium and chlorine atoms at 5000 K. Expansion through a Delaval nozzle accelerates the gas to supersonic speed cooling it very rapidly. Cooling rates are as high as 7exp 1 0 Kelvins per second. Injected hydrogen reacts with condensed titanium particles to form titanium hydride and with the chlorine to form hydrogen chloride. We have produced titanium powder at 20 kglh in a continuous reactor. Costs are projected to be lower than the Kroll Process at large enough scale. Most of the cost reduction would result from elimination of magnesium as a reducing agent and much lower capital costs.

Jan 1, 2001

By Wenxian Zhu, Patrick R. Taylor

"The small dimensions of nano-sized materials leads to novel and enhanced mechanical and physical properties. A thermal plasma reactor has been developed to study the formation of nanometer sized metal powders. A supersonic nozzle and a powder filter were designed and built. By vaporizing coarse metal powders in the plasma flame, and quenching the metal vapors through the nozzle at the rate of 107 K/sec, nanometric sized powders have been produced. The powders were collected in an airtight secondary quench-filter system. The particle size of the product power is 5 -20 nanometers, obtained through TEM analysis. The XRD analysis showed that the powder did not oxidize after the filter was handled in an inert atmosphere glove box.IntroductionNanostructured materials have been shown to exhibit improved physical and mechanical properties compared to conventional materials with larger grain sizes (1,2). There have been several methods proposed for preparing nanometer size materials. Thermally induced vapor-phase reactions have been used to produce a variety of powders. A common feature of these processes is the rapid production and cooling of condensable reaction intermediates and products, by gas-phase reactions, leading to the formation of a large number of very small particles. Thermal plasma synthesis of ultra-fine size particles has been attracting increasing interest (3,4,9-11), because it offers many advantages, especially in refractory materials processing, compared to conventional processes: (a) thermal plasma temperatures are very high(> 5000 K); (b) the rates of chemical reaction are much faster than those encountered in conventional processes; (c) high-purity materials may be obtained using fewer processing steps by collecting the product at temperatures where the by-products are in the vapor phase; ( d) the mean particle diameter can be controlled; (e) unifom sized particles may be produced with clean surfaces (these particles are particularly suitable for pressureless sintering); and, (f) high throughput per reactor volume can be achieved. In addition, the process used for generating particles determines the degree of sintering ability of the powders, since the process dictates the morphologies, the purity and its size distribution. In the future, thermal plasma synthesis nanometer size particles may play an important role in vapor phase reaction techniques and might be expected to be one of the first full scale commercial installations in the future."

Jan 1, 1998

By Jerome Feinman, Sven O. Santen

"The principles involved in the generation and application of plasma energy are reviewed briefly and the major developments in commercial and semi-commercial primary metal and alloy production are described and discussed in broad outline, with emphasis on present performance and future potential. New concepts in the application of plasma energy in primary operations are described with emphasis on the expected advantages over conventional technology and the problems that have to be solved to enable effective implementation.IntroductionThe use of plasma energy in industrial processes is generally considered to have started in 1905 with the operation of the Birkeland process for nitrogen fixation for fertilizer production. Although it seems logical to apply plasma energy to metallurgical processes, which also usually require considerable energy at high temperature levels, serious development work along these lines did not begin until the early 1970's. The reasons for this hiatus are associated in part with recognized difficulties in applying plasma energy in processes involving tonnage quantities of solids in severe industrial environments and the delicate nature of the earlier plasma generators. Another, and perhaps overriding factor, is the fairly steady improvement in efficiency and economy of most primary metal producing processes by conventional developments and modifications through the 1950's and 60's. Examples of these evolutionary changes include burden preparation and fuel injection in blast furnace applications and prereduction treatments in ferroalloy operations. By the end of the 1970's most primary metal producing processes had been optimized close to the limit, at least in terms of those operations that were able and willing to implement the developed improvements. In this context, plasma energy offered the possibility to achieve further significant improvements in primary operations where conventional means were exhausted."

Jan 1, 1988

By Kouji Mimura, Manabu Kishida, Minoru Isshiki

"Purification of metallurgical grade silicon (MG-Si) by the plasma-arc zone melting method (PZM) has been examined. The process consisted in the horizontal displacement of a molten zone heated by Ar- and 10%H2+Ar- plasma-arc under atmospheric pressure. This technique, especially using hydrogen plasma-arc, promoted the segregation of impurities from the head to the tail of the bar and the vaporization of impurities of higher vapor pressures. Metallic impurities such as Fe, Ti, Cr, Mn,. Cu, Al and Ca were reduced to less than 1 mass ppm at the head side of the Si bar. Non-metallic impurities such as boron, phosphorous, carbon and oxygen were also reduced by the zoning effect and, furthermore, by activated hydrogen atoms dissociated in the high temperature plasma-arc according to the following reaction: Q (in liq.Si) + 2H = H20. Plasma-arc zone melting with hydrogen plasma has been recognized to become an effective purification technique of MG-Si for the production of a low cost solar grade Si (SOG-Si).IntroductionDemand of high-purity Si for solar grade silicon (SOG-Si) is supposed to be further growing in the near future. The purity of SOG-Si required for the photovoltaic cell is more than six nines. An expensive semiconductor grade silicon (SEG-Si) with the purity of around eleven nines has been used to satisfy the demand. Development of techniques and processes for the production of a low cost SOG-Si is therefore necessary [l]. Although many purification techniques, such as directional solidification, plasmaarc melting and electron beam melting [1-6], and processes, such as carbothermic reduction of high purity silica [7], have been examined and proposed for this purpose, a more efficient and practical purification technique is still required.In the present work, the purification of MG-Si has been investigated using a plasma-arc zone melting (PZM) technique developed by the authors. Plasma-arc melting, which is well· known as a useful melting method for various metals and alloys, has been recognized to be efficient for refining and degassing several metals if hydrogen is added to the plasma generating gas, resulting in the so-called hydrogen plasma-arc. For example, deoxidation of Fe, Co and Ta [8,9], decarburization of Fe [9] and removal of metallic impurities from Zr, Ta and Fe [10-12] have been reported. This excellent refining effect is considered to be caused by dissociated and activated hydrogen atoms formed in the high temperature plasma-arc."

Jan 1, 2000

By Taegong Ryu

A thermal plasma process was used to synthesize nanosized tungsten carbide -cobalt composite powder, in which ammonium paratungstate and cobalt oxide were reacted with a gas mixture containing CH4, H2 and Ar. The reduction and carburization of vaporized precursors produced nanosized tungsten carbide (WC1-x) - cobalt composite powder, which sometimes contained small amounts of W2C and/or W phase. The effects of gas composition, plasma torch power, and the flow rate of plasma gas on the product composition and grain size were investigated. The grain size of synthesized tungsten carbide powder was less than 20 nm. The synthesized composite powders were also subjected to a hydrogen heat treatment to fully carburize WC1-x, W2C, and W phases to the WC phase as well as to remove excess carbon in the product. Finally nanosized WC-Co composite powder of grain size less than 50 nm was obtained.

Jan 1, 2009

By G. Scavino

A 0.5 wt.% C, 22 wt.% Mn austenitic steel, recently proposed for fabricating automotive body structures by cold sheet forming, due to favorable overall strength and ductility, exhibits plastic localizations during uniaxial tensile tests, whereas no localization happens during biaxial Erichsen cupping tests. Full-thickness tensile and Erichsen specimens, cut from as-produced sheets, were polished and tested at different strain rates. During the tensile tests, the plastic localization phenomena consist first of macroscopic deformation bands traveling along the tensile axis, and then of series of stationary deformation bands, each adjacent to the preceding ones; both types of bands involve the full specimen width and yield macroscopically observable surface relief. No comparable surface relief was observed during the standard Erichsen tests. The stress state being known to influence plastic localization phenomena, reduced-width Erichsen tests were performed with 10 to 30 mm width polished specimens, in order to explore the transition from biaxial to uniaxial loading.

Jan 1, 2009

By R. B. Nourse

The depressed market for Ferrochrome worldwide has forced most producers in this industry to scale down production. Inevitably, many furnaces have been mothballed for prolonged periods, awaiting an upturn in the Ferrochrome market. In contrast, the Platinum industry is experiencing relative stability combined with good prices and they have been looking for cash cows to take advantage of these market conditions. It is, therefore, rather convenient that Platinum and Ferrochrome producers are virtually neighbours in the Bushveld complex of South Afiica, since there is an abundance of spare furnace capacity around (albeit for Ferrochrome). Against this backdrop, Pyromet Technologies (Pty) Ltd, who are currently designing a slag cleaning furnace for Anglo Platinum, was requested to perform pilot scale testwork on a 200kW furnace, in order to establish the suitability to process platinum concentrate and converter slag in a furnace designed for Ferrochrome. This paper provides an overview of the configuration, test conditions, operation and results achieved during the testwork. It also discusses the critical issues, such as refractory consumption, copper cooling and electrical parameters that need to be addressed when converting a Ferrochrome Smelter into a Sulphide Smelter.

Jan 1, 2002

By J. Y. Foley

Platinum-group elements (PGE) are preferentially associated with chromian spinels, including high-iron chromite, magnesian-chromian hercynite, and chromian magnetite in clinopyroxene-rich upper stratigraphic portions of the Tonsina ultramafic complex in southern Alaska. Ratios of Pt:Pt+Pd are proportional to chromium content in the associated chromian spinels. The maximum PGE content of geochemical rock samples from Dust Mountain is greater than 20.000 ppb (>0.6 oz/ton) with minor gold values. The maximum PGE content of tabled chromite concentrates is 3.430 ppb (0.1 oz/ton) at Dust Mountain. 1.029 ppb (0.03 oz/ton) at Sheep Hill, and 1,749 ppb (0.051 oz/ton) at Bernard Mountain. High-iron chromite at Dust Mountain yields tabled chromite concentrates with Cr:Fe ratios between 0.5 and 1.2. Lower PGE contents are found in more chromium-rich chromitites from Sheep Hill and Bernard Mountain that yield concentrates with Cr:Fe ratios between 1.0 and 2.8. Platinum-group minerals include amalgams. arsenides. PGE alloys, and sulfides. These minerals are between 3 and 40 microns in size and are concentrated along grain boundaries and fractures of metasomatically and hydrothermally altered chromian spinel grains.

Jan 1, 1987

By R. W. Bartlett

A two step process for treating platinum group metal flotation concentrates Is described while experimental results. The process was designed to be simple and Inexpensive While yielding a high recovery and fast turnaround. Ii consists of electric furnace smelting of concentrate to remove gangue and produce a homogeneous sulfide matte containing all of the base metals and platinum group metals. Sulfide oxidation Is minimized during smelting to avoid Installing an acid plant In the second step, matte Is pressure-leached with oxygen In an acid sulfate system to dissolve Iron, nickel, ?and copper while leaving a residue highly concentrated In precious metals, and typically about 1% of the flotation concentrate mass, A batch process with oxygen titration against the base metal composition of the feed Is used to control the end point of the leach. Sulfides must be eliminated while minimizing the precipitation of hydrolysis products. The leach residue can be smelled to bullion to facilitate sampling accuracy.

Jan 1, 1989

By Christophe Thiébaut

Keywords: Pyrochemistry, Salts Treatment, Distillation The pyrochemical purification of metal generates spent salts. When this metal is an actinide such as plutonium, the slags cannot be discarded and are thus disposed in nuclear facility. In order to handle with these slags, the decision has been taken to reduce stored quantities. The development of a pyrochemical treatment is in progress in the CEA Valduc centre. The feed salt, typically composed of various Pu and Am species contained into monovalent or divalent chloride matrix, is first oxidized to convert the actinides into oxides. Then the chlorides are separated from the actinide oxides by vacuum distillation. Temperatures higher than 750°C for monochloride salts mixture NaCl/KCl and higher than 1100°C for divalent CaCl2 base salts, are required to produce an industrial flow of vaporization. Inactive qualification of the process for NaCl/KCl base salt has been carried out with lanthanide surrogates. Then, a pilot equipment, called distillator has been designed and built for production-scale distillation of NaCl/KCl and CaCl2 oxidized plutonium salts. Industrial flows of vaporization have been obtained with this pilot equipment : about 4 g/cm²/h for NaCl/KCl at 800?900°C and 1 Pa, and more than 1,5 g/cm²/h for CaCl2 base salts between 1000?1200°C at 0.1 Pa. The last step, now in progress, is the integration of the distillator into a glove box.

Jan 1, 2005

By Norberto Benitez, Christian Ludwig, Simona Regenspurg, Fabian Mendez

"Navarro is the main garbage dump in the city of Cali (Colombia). Operated since the late 1960s it collects about 1.600 tons of waste daily. The environment surrounding Navarro is highly contaminated and the pollutants released by the dump threaten human health in the adjoining neighborhoods. The goal of our project is to identify major pollutants released from the dump and their distribution in the surrounding ecosystem. In a first phase of the sampling and analysis program landfill leachate was collected and screened for heavy metals and for the most common persistent organic pollutants. This allowed us to identify the most relevant compounds on which we focused in a more detailed second phase investigation. These compounds were quantified in the vicinity of the landfill (groundwater, surface water, drinking water and soil) to get information on their mobility and possible pathways into the human body.IntroductionThe usual technique of waste disposal in most developing countries is by landfilling on not -, or not well controlled sites, where people live close by or even on the waste itself. A typical example for this practice is Navarro, the main garbage dump in the city of Cali (Colombia). Operated since the late 1960s it now consists of about 23 million tons of household and industrial waste. The dump is located on a wetland in the riverbed of the Cauca River, the main drinking water source for Cali. Two ponds of unknown permeability located next to the landfill collect a fraction of the waste leachate. During the rainy season, the ponds frequently overflow and drain into the soil (alluvial, loamy sediments) of surrounding sugar cane fields. The environment of Navarro is assumed to be highly polluted and there is evidence that it affects the health of nearby inhabitants. Specifically, the incidence of respiratory diseases was higher among vulnerable individuals (<3 and >50 years old) living in a <3 km perimeter of Navarro as compared with a control group (Solano et al., 2006). Further, a clustering of extremely rare congenital malformations (sirenomelias and cyclops) was observed in a small area during a short time period (<6 months) (Filigrana et al., 2008)."

Jan 1, 2008

By Steven M. Puricelli

Sulfuric acid plants associated with smelters, have historically been an overworked and often neglected pollution control device. They could do little more than manage the wide fluctuations in gas flow and SO2 strength from the smelter. With the introduction of flash smelting, the picture began to change, but the fluctuating batch converters continued to dictate acid plant design. More recently, the commercial use of continuous converting processes utilizing high levels of oxygen enrichment has dramatically upgraded the SO2 strength and stabilized the gas flow to the acid plant. The SO2 gas now issues continuously and at concentrations that allow for compact and, cost effective acid plants. Relieved of the burden of excessive dilution air, the heats of reaction can also be recovered as medium pressure steam and used to drive a generator, making the acid plant a net producer of power and a valuable asset to balance sheets. This concept was put into practice at the Kennecott Utah Copper Corporation smelter modernization project, located in Salt Lake City, Utah. The new acid plant, which was commissioned in June of 1995, is a sophisticated, low environmental impact, energy producing plant, worthy of review. This paper examines the key features of this acid plant, such as controlling its tail gas, by catalysis alone, to an environmentally friendly, 100 ppm of SO2, while feeding the acid plant converter with an efficient 14% SO2. The acid plant is also a prudent steward of energy resources, recovering 220,000 lb/hr of 140 psig steam from process heat which is used to generate a substantial 20 MW of gross power. Also discussed will be some of the ongoing issues, such as handling of selenium and fluorine in the gas cleaning sections, as well as a review of some. of the problems that were identified and resolved. Today&apos;s modem acid plants, by necessity, are becoming a producer of quality, valuable products, making the acid plant an asset and not a liability. Plants like Kennecott are already gaining wider acceptance and are expected to be the vision of the future.

Jan 1, 1998

By Ravinder N. Reddy

Electrochemical capacitors are charge storage devices. They bridge the gap between dielectric capacitors and batteries in terms of energy and power density. Electrochemical capacitors are classified into two types, electrochemical double layer capacitors (EDLCs) and capacitors based on pseudocapacitance. In EDLC, charge is stored at the interface between electrode and electrolyte. Carbon is considered to be prime electrode material for EDLCs due to its many favorable characteristics. In this study carbon materials are derived from thermal decomposition of catechol- formaldehyde polymers and are studied as electrode material for electrochemical double layer capacitors. Carbon electrode surface is characterized using NOVA 1200 gas sorption analyzer. It is also characterized using XRD and SEM. Carbon electrodewaselectrochemically characterized using cyclic voltammetry (CV). A highest capacitance of 110 F/g was observed in 30 wt% H2SO4.

Jan 1, 2006

By Yuchun Wang

In principle, supported liquid membranes could be an exceedingly elegant separation process. However they tend to fail by displacement and emulsification of the organic solution in the pores, which allows mixing of the feed and strip solutions. We have stabilized supported liquid membranes comprising moctylamine in nylon and PVDF supports by covering the pores with semi-permeable polyamide films, using an in-situ polymerization technique. Scanning electron microscopy demonstrates that the polyamide films are sensitive to production conditions and the nature of the support. The transport properties of stabilized supported liquid membranes for Cr(VI) are compared with those of unstabilized membranes.

Jan 1, 1998

By Michael A. Markowitz, Alok Singh

"Molecular self-assembly of phospholipids and other amphipathic molecules offers a versatile approach to form self-organized microstructures in various morphologies. Stabilization of microstructures in specific morphologies by polymerization renders them useful for practical applications in areas ranging from controlled release technology to template mediated synthesis of metals. Our efforts are focussed on the development of polymerizable biomembranes derived from phospholipids, their properties and utility e.g., as stable templates for studying chemistry at the lipid interface. Polymerized vesicles formed from mixtures of 1,2-bis(tricosa-1 O,12-diynoyl)-sn-glycero-3-phosphocholine, 1, with corresponding lipids having phosphohydroxyethanol,2, or -hydroxypropanol,3, headgroups have been used in electroless metal plating of vesicle surface with gold utilizing selective binding of Pd(NH3)4 2 + to 2 or 3. The surface bound palladium ion served as catalyst for metalization. Metalization of polymerized vesicles constructed from charge neutral diacetylenic phosphocholine,1, did not occur using this process. The headgroup structure of the negatively charged phospholipids and the degree of vesicle polymerization had an effect on the stability of the vesicles after metalization. Vesicles formed from a mixture of 1 with polymerizable diacetylenic phosphatidic acid, nonpolymerizable 1,2- dipalmitoyl phosphohydroxyethanol or 1,2-diacyl phosphohydroxyethanol (from soy lecithin) were not stable to metalization process. The metal coating of the vesicles was examined by electron diffraction and revealed that the gold metal on vesicles was polycrystalline and face centered cubic. The results demonstrate the utility of polymerized synthetic membranes as template for easy and efficient synthesis of nanoparticles. IntroductionPhospholipids, synthetic or natural, provide a simple and straight forward route to construct membranes in a variety of morphologies due to their inherent property of selforganization in the presence of water[1]. Vesicles are closed spherical structures comprised of concentric walls made from lipid bilayers. Vesicles are morphologically simple structures with enormous technological potential. Polymerizable phospholipids prepared by incorporating a polymerizable group in the molecules demonstrate physical properties comparable to their non-polymerizable counterparts and have the added virtue of providing enhanced physical and chemical stability to the membranes[2,3]. The size, shape and properties of the organized assemblies are dependent on the lipid structure and the nature of the aqueous environment[4,5]. The headgroup geometry, surface charge density, and spatial arrangement of the phospholipids are known to affect the surface behavior of the lipid membranes, which is evident through their interaction with other molecular (hormones, antigens, antibodies etc) or lomc species. Since phospholipid headgroup structure and charge can be modified either synthetically or by chemical perturbation of the aqueous medium (e.g., pH or ionic strength), phospholipid membrane surfaces offer a potential for developing novel strategies in those areas which involve the use of molecular reactive sites. One such strategy which could be envisioned explores the use of molecularly engineered phospholipid assemblies to design and prepare template structures to regulate formation of ordered materials [6]."

Jan 1, 1994

By Ashish D. Patel, Ramesh S. Minisandram

"Vacuum Arc Remelting (VAR) is the final and, hence, critical melting step for the production of a sound, segregation-free ingot for the manufacture of alloys used in rotating components in aircraft engines. A mathematical model for this process has been developed by the Specialty Metal Processing Consortium (SMPC). The model predicts temperature distribution in the solidifying ingot, flow in the molten metal pool, and the electromagnetic field in the ingot. These predictions may be used to estimate the effect of melting parameters on the pool profile in the ingot. In this paper, typical pool shapes and flow fields during VAR of Alloy 718 and Ti-6Al-4V are presented. The differences in the pool profile are primarily due to vastly different melting conditions. The model predictions are compared to the observed pool shapes from industrial-size VAR ingots.1. IntroductionVacuum Arc Remelting (VAR) is a process in which an electrode is melted in vacuum by the heat from a DC electric arc. Metal droplets from the electrode fall into the molten metal pool, which solidifies in a water-cooled copper crucible to form the ingot, as shown in Figure I. The ingot obtained from VAR is sound, and has superior cleanliness and chemical homogeneity. Hence, the process is the final melting process for most nickel-base superalloys and titanium alloys used in the manufacture of critical rotating components (discs & blades) of aircraft engines. Modeling of this process provides an insight into the effect of melting parameters on the molten metal pool in the solidifying ingot, which is a key first step in process optimization and defect prevention. In this paper, typical pool shapes, both measured and predicted, for VAR of Alloy 718 and Ti-6Al-4Vare presented. Alloy 718 is the most common VAR-processed nickel-base superalloy; whereas Ti-6Al-4V is the ''workhorse"" alloy for titanium-based alloys."

Jan 1, 2004

By A. J. Rigby

Current practices employing porous plugs to inject nitrogen into molten copper during primary smelting are described. Nitrogen stirring increases heat transfer to the bath, eliminates temperature stratifications, and improves efficiency during the steps of desulfurization and deoxidation. The opportunity to use porous plugs as the means to introduce reducing gases to deoxidize copper is also discussed. Previously reported laboratory results using porous plugs, which point to very high utilization efficiencies of hydrogen when used as the reducing gas, are again reviewed. Advances in the design of the porous plug, and the introduction of a system enabling external replacement of plugs is also discussed.

Jan 1, 1999

By Rejane Tubino Geyer

The volume of electric arc furnace (EAF) plus oxygen (BOF) slag produced yearly in the world is about 84 million ton. Because of this, the study of recycling processes as a way to solve the storage problem of these slags rise in importance. There are, however, some inconvenients on using this byproduct: lime, which takes part of the process of steel production, remains as a non-reactive raw product in the slag. Since lime reacts in presence of humidity, forming expansive compounds, slag use is strongly limited. There are some utilizations for the electric arc furnace and oxygen slag in the Civil Construction Industry, mainly as base, subbase and asphalt covering in highways. However, independently of the type of recycling, a period of "cure" of about six months is necessary. Because of this slow cure process this byproduct may turn non-competitive in some regions if compared, for example, with the natural aggregate. The objective of this work is to present the flowsheet of the slags production as a residue both at the electric and oxygen steel plants and, through a bibliographic review, to analize the possibilities and limiting factors for the use of steelmaking slags in the Civil Construction Industry.

Jan 1, 1996

By Stefan Mutz

In Germany the automobile recycling is regulated by law. Current legislation requires that by the year 2015, eighty five w.-t. % of the components from used cars ill be materially recycled. Whilst for 10 w.-t. % of the materials a thermal utilization is certified, there are still some concrete questions that remain unanswered regarding the usability of single fractions. The recent innovative approaches to the concepts of used cars dismantling do not alter the fact that the majority of the materials of used cars still have to pass over the shredder and the connected processing aggregates. The status of the so called SLF (Shredder light fraction) which is about 25 w.-t. % w.-t. in used cars, has not been satisfactorily clarified. Furthermore questions still remain regarding the separation of the NMSF (nonmagnetic metal shredder fraction) which has to be separated in the single metallic fractions like stainless tell, copper, brass, zinc, etc. Attempts of optimization can be found. This paper analyses some of the difficulties being encountered by the automobile recycling industry in Germany, before reviewing some of the innovative approaches that the industry has introduced. Finally the paper goes on to describe the potential of automatic picking. Examples of a series of tests, utilizing this technology, in which a variety of products from a range of shredders were isolated are described in detail. This new technology provides a range of applications to the automobile recycling industry.

Jan 1, 2002

By Ilie Butnariu

Steel manufacture in VOD procedure needs a very attentive correlation and pursuit of the technological stages ,on the background of keeping the influence factors within best performances zones. For a better co-ordination of the main stages specific to this process ,this work presents a detailed study of the optimization possibilities for each stages ,beginning with the furnace charging ,going on with the pre-aftinage and aftinage stages in the electrical furnace and then with the refinement stages in the VOD installation. One has intended the effective emphasis of the main influence factors with global implications on the process and especially on the purity and quality of the stainless steel ,Among the main novelties proposed by this work , we can emphasize the following: - a computer assisted charging method ,with the possibility of using a large scale of wastage, also respecting the density proportions of the components of the charges; - the advanced recuperation of the elements of the charge by reducing the combustion of the valuable elements ; - the optimization of the oxygen blast conditions and of the aftinage stage ,by establishing some calculations concerning critical carbon content , that requires the oxidation to be continued very carefully; - the simulation of the thermic and chemical parameters by modeling the alloying process of the stainless steel in the case of some large amounts of additions.

Jan 1, 1994