Search Documents

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'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 Satian Niltawach

Iron sulphate jarosite through which iron in zinc sulphide concentrate feed is removed from the production circuit of conventional roast-leach-electrowin process, is chemically unstable and environmentally hazardous even if it is mixed with lime. If zinc silicate ore is used at similar chemical conditions in place of calcine in the jarosite precipitation, the resultant silico-jarosite residue having been mixed with lime is chemically stable and environmentally friendly. The recovery of zinc from silicate ore is also higher than that from calcine.

Jan 1, 1994

By T. T. Chen

The manganese oxide scales, consisting mainly of MnO2, characteristically occur in banded colloform structures which adhere to porous layers of PbSO4 and PbO2 that oxidized from the rolled Pb-0.7% Ag anodes. Hydrous Mn oxides, Mn3O4 and amorphous Mn oxides are believed to be also present. Tiny particles of gypsum, PbSO4, SrSO4 and AgCl are entrapped in the colloform masses. The gypsum originated from the Zn electrolyte; strontium carbonate was added to the ZnSO4 solution to control Pb, and silver originated from the anodes. Some of the colloform bands contain minor amounts of Pb, implying a limited degree of dissolution of the Pb during electrolysis. Other colloform bands incorporate trace amounts of Zn. Colloform structures permeated with silica gel are presumably caused by the high silica content of the electrolyte.

Jan 1, 2009

By Song Ning

The main mineral constituents of phase-transformed chalcopyrite are CuS and FeS2. CuS is more soluble than FeS2 in an acidic CuCl2 solution with presence of excessive NaCl, so that FeS2 could be removed as solid residue from a leached solution. The experimental results showed that the efficiency of the copper leaching is heavily determined by the following two factors: a) The degree of the chalcopyrite phase transformation to CuS and FeS2 b)The concentration of Cl during the leaching, specifically whether there is enough excessive Cl existed. I t was found that when the Cl in the solution is not excessive, the slowest step of the leaching is the dissolution of Cu2Cl2.

Jan 1, 2006

By Ho Jung Heo

The proper control of slag composition is a dominant factor affecting yield of iron as well as dephosphorization efficiency in an electric arc furnace (EAF) operation. Moreover, thermophysical properties of slags such as viscosity are strongly affected by the changes in slag composition. Slag foaming, which is also a function of viscosity, is directly connected with the yield of iron and thus optimum slag chemistry are highly required in view of thermodynamics and physical properties. Therefore, we analyzed the slag composition in commercial melt shop (70 ton EAF) with the aim of higher yield of iron as well as higher dephosphorization during EAF process.

By Dilek Kirgöz, Onuralp Yücel, Murat Alkan

"In this study, Mo containing Fe-based alloys, such as Fe-Ni-Cr-Mo, were synthesized using a mixture of Fe203-NiO-Cr203-Mo03 powders reducing with Al powders by metallothermic process which is a high energy efficient, fast and low-cost production technique for synthesis of cast alloys and advanced ceramics. Detailed thermochemical studies were simulated by using FactSage 6.2 Thermochemical software in order to calculate adiabatic temperature of the reactions and effects of initial molar composition on the final products. In the metallothermic processes, effects of stoichiometric Al addition and addition of the oxide powders (Alz03, Si02, CaO, MgO) on the metal recovery and compositions of final alloys were carried out. Final products were characterized by using chemical analysis (AAS), XRD, XRF and SEM/EDS techniques.IntroductionSelf Propagating High Temperature Synthesis (SHS) has significant advantages compared to the high technology furnace applications, such as very short processing time, simple operation, low energy requirement and low cost [l, 2]. In a SHS process, the ignition starts the combustion and propagates throughout the reactant mixture yielding the desired product. However, the disadvantages of the process such as inhomogeneous or unreacted products due to undesirable reaction rates needs to be overcome by changing some parameters such as ignition temperature, particle size, additive, atmosphere etc. [3, 4]. This work aims to establish a scientific and engineering background in the production of some cast Fe based alloys (Fe-Ni-Cr-Mo) which are used as surface coatings, wear-corrosion-oxidation resistive applications via SHS (Self Propagating High Temperature Synthesis) metallurgy which is attractive process technique regarding fast and low-cost production ability of cast alloys."

Jan 1, 2013

By Abhishek Asthana

The incineration of Municipal Solid Wastes (MSW) is an attractive process for reducing the volume of the wastes and recovering their energetic value, which, however, requires to be strictly controlled in order to limit its impact on the environment. In this context, we have undertaken the mathematical modeling of the different sections of a typical incineration plant. The combustion of the waste bed, usually carried out on a moving grate, is at the core of the process. This paper presents the 2-dimensional, steady-state model that we have developed for simulating the MSW combustion. The model describes gas flow through the porous waste particle bed, the gas-solid reactions, conductive and radiative heat transfers, drying of the feed, its pyrolysis and the emission of volatile species, combustion of the pyrolysis gases, the formation of char and its gasification by water vapor and carbon dioxide, and the consequent reduction of the bed volume. Pyrolysis kinetics distinguish between cellulosic and non-cellulosic materials and are experimentally derived from our laboratory measurements. The calculated results give a deep insight into the various involved phenomena, an example being the complete consumption of oxygen in a large zone of the bed and the related appearance of a char gasification zone. The influence of various operating parameters, like the temperature and flow rate of primary air, is presented and explained. Finally, the effect of stirring the waste bed on the moving grate is also analyzed.

Jan 1, 2006

By Vince Newberry

Alcan Rolled Products at Oswego, New York, commissioned Recycle II during May of 1995. Recycle II is an advanced technology UBC recycling facility designed to meet the most stringent environmental standards enforced to date in the United States, particularly with respect to NO, and particulate emissions. This paper addresses the exacting requirements and strategies of Alcan's Recycle II project andThorpe Technologies' design considerations and solutions for the supply of environmentally favorable melting furnace and delacquering systems. The furnaces are equipped with low NOx regenerative burners and furnace pressure and hearth gas flow controls designed specifically for processing the hearth gases through baghouses. The delacquering system is a new generation Apros concurrent flow unit designed for low NOx emissions.

Jan 1, 1995

By J. P. R. deVilliers

A procedure is described whereby gold-containing calcined concentrates and leach residues from refractory gold ores are smelted with carbon to form a small amount of metal. The gold is liberated upon smelting, and is collected in the molten metallic phase, which is easily separable from the slag. The metallic phase consists of approximately 1 to 15 per cent (by mass) of the material after smelting, and the gold content is generally upgraded by a factor of greater than 6 compared with that of the original roasted material. Recoveries better than 95% have routinely been achieved. The quenched metal contains predominant Fe-Ni alloy, as well as minor Fe sulphides and Cu-Fe sulphides. Trace amounts of Fe-Ni arsenide and Au-Cu alloy are also present. The gold content of the metallic phase can be increased further by oxidation of the hot metal in the presence of silica or slag. This will reduce the amount of metal, and will concentrate the gold in a smaller volume. The metallic phase can then be treated hydrometallurgically to recover the nickel and the gold.

Jan 1, 1989

By John Jiang, Yeonuk Choi, Olivia Wang, Gus Van Weert

"As part of a general review of processing double refractory ores through Barrick Gold's autoclaves/CIL facility at Goldstrike, Nevada, blanking the gold cyanide adsorbing native carbon in the ore with hard (m.p. >55°C) paraffin wax was proposed. To avoid interference from other ore constituents in the exploratory testwork, commercial activated carbon was substituted for native carbon in the ore to establish the best conditions for de-activation of carbon with molten wax.IntroductionDouble refractory gold ores present two barriers to gold extraction. The first is generally a physical barrier: the gold is encapsulated or dispersed in a matrix which is impervious to the gold lixiviant. In most cases, including the Goldstrike deposit, this involves a pyrite or arsenopyrite matrix, although minor gold may also be dispersed in competent silica (quartz) or iron oxides. Gold can be rendered accessible by oxidative destruction of such sulphide matrices. At Goldstrike this is practised by roasting and autoclave oxidation (POX). It is the latter route to which this paper refers.The second barrier refers more correctly to gold recovery. Gold may be extracted from the autoclave oxidized solids with cyanide, forming a gold cyanide complex. One characteristic of this complex is that it adsorbs on graphitic surfaces. This behaviour is used advantageously on a large scale by gold millers, who use man made activated carbon particles to remove the gold from solution during leaching: the Carbon-In-Leach, or CIL process. The gold bearing carbon particles are larger than the ore solids and can be separately recovered by screening. Goldstrike uses the CIL technology to recover gold after autoclave oxidation."

Jan 1, 2012

By František Molnar, Zsolt Szentirmai, Juraj Schmiedl, Felix Sekula

"Hydrometallurgical nickel production in Sered Nickel Plant (Slovakia) that treated roasted Albanian ore left behind a considerable amount of the solid leaching residue. About 6 million tons of this fine-powder residue containing approximately 52 wt.% of iron in the form of oxides is to the present day stored in a stockpile. However, its iron content makes it a potentially interesting secondary raw material for iron production. This secondary raw material is not, unfortunately, suitable for direct treatment in iron and steelmaking processes.This paper presents results of the laboratory tests of pyrometallurgical method of processing of the leaching residue by its roasting and subsequent refining melting. The objective of the selective reducing agglomeration roasting was to reduce iron oxides and to simultaneously avoid reduction of chromium oxides and silica. Refining melting is carried out in an inert atmosphere. The products of melting are technically pure iron and slag.IntroductionThe leaching residue stockpiled on waste dump near already non-existing Nickel Plant Sered, Slovakia, is considered to be one of the most important environmental burdens in this country. The 40-years of an on-going effort focused on finding the methods for extracting metals and thus remove the waste dump have not been successful [1,4,5,6]. From the literature survey it is evident that past investigations have been following three main routes:1.Removal of chromium by mineral processing methods prior to its metallurgical treatment to achieve final chromium concentrations below 0.3 wt.%.2.Pelletization of solid leaching residue and its subsequent reduction in blast furnace and steelmaking plant and simultaneous removal of chromium.3.Pelletization of solid leaching residue followed by metallurgical processing of preliminary reduced semi-product in electric arc furnace (EAF) accompanied by partial reduction of chromium."

Jan 1, 2008

By Kee Jeung Lee

In this study the characteristic factors and formation mechanisms for the hydrothermal preparation of a -quartz crystal powders were investigated to find the optimum synthetic conditions. The degree of Q -quartz crystal face development depended on the relative growth rate of a particular form that varies considerably with the degree of supersaturation, the reaction temperature, the concentration of mineralizers, and the presence of seed crystals in the feedstock. Alkali hydroxides and alkali halides were found to be effective in the reactions as mineralizers, which added in order to increase the solubility of the feedstock. The fine Q -quartz crystal powders were obtained in the temperature range of 250-450% and pressure range of 100-300atm. As the concentration of mineralizers increased, the particle size of crystalline powders became smaller at lower reaction temperatures. The fractional size distribution of synthetic crystal powders was depended on the hydrothermal conditions. As the reaction time and the amount of seed crystals increased, the width of particle size distribution became narrower. The weight mean particle size was in the range of 1 to 10m. The characterization of the products were carried out using XRD. SEM. PSA, FT-IR, Raman spectrometer.

Jan 1, 1997

By Muhlis Nezihi Saridede, Burak Birol

"Plastic wastes become a huge problem day after day due to the growth of plastic industry. Hence, plastic wastes are used as a raw material for other industries to eliminate this problem. Polyethylene Terephthalate (PET), which is a commonly used for plastic bottles, may be used as a reductant for iron production because of its C and H content. In this study, composite pellets containing iron ore concentrate, flux and reductant were prepared. Crystallized PET bottles and coke were used as reductant after ground. The prepared pellets were reduced at 1400°C for 30 min. and iron nuggets were produced successfully. Usage of waste PET purely as reductant in composite pellets gives a higher metallization degree and proper carbon content than coke or PET and coke mixture.IntroductionPlastics can be seen everywhere, especially at packaging industry in our common life. The increase of plastic usage ends up with an important problem, the increase of plastic wastes. Many studies have been carried out about usage of plastics as reductant in blast furnace such as Ogaki et al.[1], Heo and Baek [2], Saridede [3], Minoru et al.[4], etc. Besides, Kato et al. [5], Nomura and Kato [ 6] and Rongfang et al. [7] have pointed out the use of plastics in coke ovens regarding to its calorific content. In EAF steelmaking, a mixture of coal/coke and plastics can be used as an energy resource instead of only coal or coke. [8] Also, the usage of PET and PC in self-reducing composite pellets increased the reduction rate. [12]PET (Polyethylene terephthalate ), which is commonly used for soft drink plastic bottles, is an important municipal waste due to its C and H content. Its molecular formula is (C10H8O 4)n. Demir and Dincer showed that PET can be crystallized at 250°C to have the ability to be ground to a size of -100 µm. [11]"

Jan 1, 2011

By Florian Kongoli

While calcium ferrite slags have been successfully used in continuous copper converting for the last 30 years, ferrous calcium silicate slag was proposed about 8 years ago as an additional alternative for copper smelting. Although both slags are normal extensions of each other their phase relations have not been completely clarified. In this paper the liquidus relations of both slags have been quantified at various areas that cover both of them. The existing experimental data have been first reviewed and discussed in relation to the solidification procedure. An original physical model is then used to predict various diagrams of the liquidus surface of both slags. It is shown that the ternary liquidus diagrams normally used for FeOx-SiO2-CaO system are not suitable for industrial slags. The new model diagrams of Fe/CaO versus SiO2 and Fe/SiO2 versus CaO as well as Fe/CaO versus Temperature and Fe/SiO2 versus temperature are proven to be much more convenient for ferrite and ferrous calcium silicate slags. Based on these diagrams the effect of SiO2 and CaO on the melting temperature is quantified. The effect of Cu2O is also quantified through the model. Some Fe/CaO versus Cu2O and Fe/SiO2versus CaO at various copper contents are predicted and the results show good agreement with the experimental data. It is also shown that in the presence of liquid copper, Cu2O is dissolved in the slag depending on the oxidation degree of the system and might lower the liquidus temperature. Some discussions are also presented taking into account plant observations and important conclusions are drawn for copper smelting and converting

Jan 1, 2006

By Florian Kongoli

While calcium ferrite slags have been successfully used in continuous copper converting for the last 30 years, ferrous calcium silicate slag was proposed about 8 years ago as an additional alternative for copper smelting. Although both slags are normal extensions of each other their phase relations have not been completely clarified. In this paper the liquidus relations of both slags have been quantified at various areas that cover both of them. The existing experimental data have been first reviewed and discussed in relation to the solidification procedure. An original physical model is then used to predict various diagrams of the liquidus surface of both slags. It is shown that the ternary liquidus diagrams normally used for FeOx-SiO2-CaO system are not suitable for industrial slags. The new model diagrams of Fe/CaO versus SiO2 and Fe/SiO2 versus CaO as well as Fe/CaO versus Temperature and Fe/SiO2 versus temperature are proven to be much more convenient for ferrite and ferrous calcium silicate slags. Based on these diagrams the effect of SiO2 and CaO on the melting temperature is quantified. The effect of Cu2O is also quantified through the model. Some Fe/CaO versus Cu2O and Fe/SiO2 versus CaO at various copper contents are predicted and the results show good agreement with the experimental data. It is also shown that in the presence of liquid copper, Cu2O is dissolved in the slag depending on the oxidation degree of the system and might lower the liquidus temperature. Some discussions are also presented taking into account plant observations and important conclusions are drawn for copper smelting and converting

Jan 1, 2006

By Florian Kongoli

While calcium ferrite slags have been successfully used in continuous copper converting for the last 30 years, ferrous calcium silicate slag was proposed about 8 years ago as an additional alternative for copper smelting. Although both slags are normal extensions of each other their phase relations have not been completely clarified. In this paper the liquidus relations of both slags have been quantified at various areas that cover both of them. The existing experimental data have been first reviewed and discussed in relation to the solidification procedure. An original physical model is then used to predict various diagrams of the liquidus surface of both slags. It is shown that the ternary liquidus diagrams normally used for FeOx-SiO2-CaO system are not suitable for industrial slags. The new model diagrams of Fe/CaO versus SiO2 and Fe/SiO2 versus CaO as well as Fe/CaO versus Temperature and Fe/SiO2 versus temperature are proven to be much more convenient for ferrite and ferrous calcium silicate slags. Based on these diagrams the effect of SiO2 and CaO on the melting temperature is quantified. The effect of Cu2O is also quantified through the model. Some Fe/CaO versus Cu2O and Fe/SiO2versus CaO at various copper contents are predicted and the results show good agreement with the experimental data. It is also shown that in the presence of liquid copper, Cu2O is dissolved in the slag depending on the oxidation degree of the system and might lower the liquidus temperature. Some discussions are also presented taking into account plant observations and important conclusions are drawn for copper smelting and converting

Jan 1, 2006

By J. N. Hryn

This paper describes some of the work done in Phase 1 of a multi-year, five-phase program aimed at demonstrating the economic feasibility of producing commercial-scale quantities of commodity materials derived from salt cake residue-oxide. The amount of salt cake generated annually in the U. S. is estimated to be 510,000 tons, including 340,000 tons of residue-oxide. Used beverage can (UBC) processing accounts for the majority of residue-oxiae that could be made available for further processing into commercial products. To characterize the composition of residue-oxide. eight residue-oxide samples from various secondary processors were obtained and analyzed. Surprisingly, the composition of residue-oxide was found to be independent of source or alloy family being processed, with? the exception of slightly elevated silicon levels in 3XXand UBC residue-oxide samples. Major phases detected in the residue- oxide were? alumina, spinel, and aluminum hydroxides. Preliminary economic analyses indicated that the refractory market appears to be the best choice for high value-added products produced from residue-oxide with minimum processing. Bench-scale tests indicated that low silicon containing residue-oxide is ready to enter this market, but the elevated silicon content of UBC and 3XX residue-oxide preclude this possibility. A separation technology should 'be developed to remove silicon-containing . species from the alumina and spinel values Present in residue-oxide. This technology would then allow UBC and 3XX residue-oxides to be converted to significantly higher value-added products.

Jan 1, 1995

By A. Siegmund, R. D. Prengaman

Lead anodes used in zinc electrowinning generally contain 0.5 - 1.0 % silver to reduce the rate of corrosion over the service life. For good quality zinc, the cathodes must contain less than 10 ppm lead. In order to reduce the lead contamination of the cathode, the lead anode must become coated with a protective layer of Pb02/Mn02. The formation of this layer may take as long as 30 - 60 days, during which time zinc production is substantially reduced and the cathodes are contaminated with lead. To improve the mechanical properties of Pb-Ag-anodes alloying elements such as calcium, strontium, barium and others are added. The production of cast lead-silver or lead-silver-calcium anodes often results in the formation of numerous holes, voids or laps in the anode surface that can initiate localized internal corrosion. Based on the experience as the major supplier of rolled anodes for copper electrowinning, RSR Technologies has developed an improved anode for zinc electrowinning. The anode consists of a rolled Pb- Ag-Ca-alloy with a controlled surface grain structure. It forms an adherent protective oxide coating within 2 - 3 days when placed in an electrowinning cell. The preferred calcium and silver contents of the alloy are 0.03 - 0.08 % and 0.3 - 0.4%, respectively. Rolling sheets significantly reduces the presence of internal porosity or laps. The lack of defects results in long anode life. The rolling also produces a uniform grain structure to which the corrosion product readily adheres, thus significantly reducing the conditioning period.

Jan 1, 2000

By Kouichi Nakano

Austenitic stainless steel, which includes nickel for stabilizing austenitic structure, is used for various purposes, for example, for structural material, corrosion-resistant material, biomaterial etc. Nickel is set as one of the rare metals and economizing on nickel as the natural resources is required. On the other hand, nickel is one of the metals that cause metallic allergy frequently. Therefore, high nitrogen stainless steel, where nitrogen stabilizes austenitic structure instead of nickel, has been developed in Japan and some of the foreign countries for the above reason. When high nitrogen stainless steel is fused and bonded, dissolved nitrogen is released to the atmospheric area, and some of the material properties will change. In this study, we bonded high nitrogen stainless steel by stud welding process, which is able to bond at short time, and we evaluate joint performance. We have got some interesting results from the other tests and examinations.

Jan 1, 2016

By Batric Pesic

A hydrometallurgical process for recovery of Zn and Mn from Bunker Hill Water Treatment Plant sludge was developed. The process is unique because it treats an unusual combination of metals, Zn and Mn. Another non-standard feature of the process is that leaching takes place with ~S04 in the presence of a reductant (SO2). Zn and Mn are recovered simultaneously by electrowinning, Zn on a cathode and Mn on an anode, as MnO2 The major purpose of the process is to detoxify the sludge by removing toxic heavy metals. The recovered metal values could be marketed to offset the overall costs of water and sludge processing. This work is presented in two separate parts, 1. Leaching and Solution Purification, and II. Electrowinning. This paper covers only the first part of the hydrometallurgical process: Leaching and Solution Purification. Initially, the paper briefly discusses the history of the pollution problem at the Bunker Hill Superfund Site, the origin of heavy metals in the mine waters, and the development and use of the water treatment plant. The leaching of sludge was examined as a function of the following parameters: constant vs. initial pH, initial vs. delayed addition of SO2, temperature, and pulp density. It was found that leaching with H2SO4 at pH 2.0 for 15 minutes (at 60°C), followed by S02 addition for another 15 minutes, could completely dissolve Zn and Mn. Solution purifIcation was done in three stages. In the first stage iron was removed by adjustment of pH (to pH 5.0) and oxidation offerrous to ferric iron (with H2O2). In the second stage, Cu and Cd were removed by Zn dust cementation. Finally, Co and Ni were precipitated with the organic reagents 1-2 nitroso-naphthol and nitroso, respectively. Electrowinning of Zn and Mn is discussed separately in Part II of this paper.

Jan 1, 1996