Search Documents

By Tarek M. Abd El Hamid, Suzane Ali

"Treatment of industrial waste materials is created serious problem in Egypt. Aluminium sludge is generated as a by-product from aluminium household industry which contains significantly high alumina content exceeding 90%. This by-product randomly disposed and creates serious environment problems to locate community. To develop the treatment process of this material, the recovery of high purity alumina and identify the potential application is being the primary objective, This paper represents the recovery process of alumina process waste sludge High purity alumina material <99.8% aluminium oxide with originate particle size 0.125-0.420mm and apparent density 0.39g/cm3 was obtained with a specific surface area 139m2/g. Alumina produced was modified by cerium oxide doped alumina. The catalytic activity and selectivity was investigated in conversion of iso-propanol via dehydrogenation reaction yielding only acetone indicating an excellent selectivity the dehydrogenation. The presence of 10% CeO2 increase in the catalytic activity of 82% for the originated alumina. Introduction Approximately 20 thousand tons of aluminium waste produced in Egypt in 2006 with increasing amounts expected in succeeding years. A part of this waste contains organics impurities which coexisted with aluminium waste as a result of manufacture final aluminium products, waste usually content <1 to 2 wt% of organic carbon. It's generally admitted that the organic species are present in the form of lubricant oils used in rolling and pressing equipments for aluminium sheet. Both industry and government face possible high-cost disposal problems that more magnified by large volume of waste produced. The alumina recovery leachable study conduct in this paper had the following objectives: 1- Develop a process that can provide an environmentally acceptable residue and also recover the available alumina. 2- Evaluate the alumina produced in terms of grade and catalytic application."

Jan 1, 2008

By Isabel Lázaro

A detailed study has been undertaken into the electrochemistry of the leaching of chalcopyrite in acidic solutions containing ferric ions. Mixed potential measurements have shown that the maximum potential achievable on a chalcopyrite disk in a ferric sulfate medium lies within the so-called passive or prewave region in the anodic behavior of chalcopyrite. The very low current densities due to the anodic oxidation of chalcopyrite at potentials in the region of the mixed potential has made studies of the initial stages of dissolution difficult. However a careful rotating ring-disk electrode (RRDE) study has enabled data to be obtained for the stoichiometry of the initial dissolution reaction to be obtained. Thus, in addition to the detection of soluble iron and copper as products in this potential region, a soluble sulfur species has also been detected. A comparison of the experimental with the expected collection efficiencies of the products on the ring has revealed that this soluble sulfur species is likely to be thiosulfate. The characteristic transient anodic behaviour of chalcopyrite in this potential region has been interpreted in terms of a rate limiting solid-state diffusion process. Thus, extrapolated rates based on reported measured solid-state diffusion coefficients for the mineral at elevated temperatures have been shown to be consistent with the potentiostatic current-time transients. Furthermore, comparative studies of the anodic characteristics of the copper sulfide minerals covellite and bornite has confirmed their greater reactivity in this potential region. The results of this investigation have been combined with a parallel study of the non-oxidative behaviour of chalcopyrite in order to derive a model for the dissolution process which is consistent with other published studies of the electrochemistry and dissolution of the mineral.

Jan 1, 2003

By J. M. Tourre

1995 have seen a continuation of a positive trend in the Rare Earth industry The availability of a greater diversity of Raw Material has brought additional flexibility to the Producers permitting better economics China remains the major raw material source; Chinese concentrate producers have increased capacity in 1995 (Baotou, Sichuan, etc) China&apos;s role in the Rare Earth industry will continue to evolve; the acquisition of a majority equity position by San Huan/CNNC will have a significant impact on both the Rare Earth and Magnet markets Chinese producers are increasing the quality of their products and realize their true values Chinese market, itself, is also changing as the internal needs for separated rare earth&apos;s grow Already already producer of Lamps, Loudspeakers, Magnets, and TV tubes, China is in an unique position where the potential of its internal market might be more promising than the prospects outside China 1995 has also seen the application market become more diverse and complex. There are new applications growing at a very strong pace (such as battery alloy), applications that are now penetrating their target markets with significantly increased growth rates (such as bonded NdFeB), and some applications that became more complex requiring much more sophisticated products (such as catalysis). Rare Earth producers have to spend significant ressources in order to monitor the market trends in order to predict the demand and then adjust their raw material mix. Even though there is a greater diversity of raw material available, there is still some Rare Earth elements that are in excess, while other are just in balance. As a consequence rare earth producers invest heavily in R&D in order to develop new applications for these excess elements.

Jan 1, 1997

By G. G. Krishna Murthy

Several experiments were conducted to determine the rates of heat transfer coefficients of CaO-SiO2-A1203-FeO slags at temperatures in the range 1623-1823 K The experimental technique involved measuring heating rates of a solid specimen, sub¬merged in slag phase, using a temperature probe made of Pt\ 10%Rh-Pt. Effect of %FeO (3-10%), %FeS (0.1-0.68%), %P205 (0.2-3.0%), %MgO(5-6%), and %MnO (0.96-3.84%) present in the slag on overall heat transfer coefficient, U, of slags was investigated. Simple first order heat balance equation in combination with experimental plots rising temperature of solid specimen versus time were employed to determine the values of U. The values of U determined in the present investigation were present in the range of 70-260 cal/Ks.m2. The value of U increased with increasing the slag temperature. The values of U were not effected by increased amounts of sulfur in the slag phase. The increased concentrations of MgO, FeO, MnO, and P205 in the slag phase decreased the values of U. On the other hand, the increased amounts of Fe2O3 in the slag phase increased the value of U. Comparison of the results, obtained using the slag bath stirred by argon injection, with those determined without any stirring indicated that both radiative and conductive heat transfer mechanisms are important even at high temperatures.

Jan 1, 1993

By Ricardo Badilla-Ohlbaum

Copper has been used by man for a very long time and unlike certain other metals, it is an essential element for life. Its toxicity arises both from a deficit and excess copper exposure/intake. The focus of the current discussions in countries of the European Union (EU) and in some USA States, is based on the concerns, independent of the scientific facts and the economic status of these claims, of the negative influence of copper and other metals on health and the environment. These discussions have influenced the new regulations of copper in drinking water, and the approach to regulate the appropriate levels of copper in surface water, soils and sediments. To illustrate the challenges ahead for copper, the evidence by which the current US Environmental Protection Agency (USEPA), the World Health Organization (WHO) and EU recommendation and regulations regarding copper in drinking water have been derived is presented and discussed. The gaps between the demands for new standards of health and the environment and the practical scientific tools to achieve these goals are presented, and the need to develop new regulating paradigms is also illustrated. The introduction of methodologies for the regulation of essential elements and acute inorganic substances in drinking water is discussed, as well as the status of the present approach contained in the International Program of Chemical Safety Environmental Health Criteria, (EHC) N° 170. The impact of the possible restrictions on the use of copper in the EU because of health and environmental concerns in terms of the world market for copper is discussed.

Jan 1, 1999

By A. K. Riihimäki

The description deals with duplex stainless cast steels and austenitic high molybdenum steels used in pumps for severe condition service. The main modem nitrogen alloyed duplex cast steels are presented in the ASTM standard A-890. Two grades of high molybdenum austenitic stainless steels there are presented in ASTM A-744 (-96) standard i.e. CN-3MN and CK-3MCuN. The latest and most corrosion- resistant stainless steel grade is AVESTA 654 SMO?. Avesta Sheffield the trademark owner has granted Ahlstrom Pumps license to produce the material. This new stainless steel as pump material for severe service has improved properties in the hydrometallurgy and electrorefining processes of metal and especially in the copper industry compared to duplex stainless steels. The paper deals briefly with the foundry process to manufacture high alloy stainless steel pump castings. The AOD-method (AOD= Argon Oxygen Decarburization) is an important prerequisite for the melting of low carbon, high chromium and molybdenum alloyed nitrogen steels. The properties of these steels are included. The main topic is the corrosion resistance of the above-mentioned pump materials in severe service. Results of short-time erosion and corrosion tests are discussed and compared with the results of plant tests. Practical results of pump materials performance in severe service for the copper industry are given. The new high alloyed cast stainless steel (main elements; Cr-24%, Ni-22%, Mo-7,3% and N-0,5%) has shown improved corrosion and erosion properties as process pump material in several severe service applications e.g. in the metal industry.

Jan 1, 1999

Testing is in progress to address compatibility issues with regard to long term storage of plutonium in contact with two different intermetallic systems. The two intermetallic systems are: 1. dental amalgam, i.e., mercury plus silver alloy powder, and 2. liquid gallium alloy plus copper powder. Both of these are plasto-metallic materials that undergo a solidification reaction at room temperature. Each system is allowed to react in contact with both high-purity alpha plutonium and a delta stabilized plutonium alloy at varying temperatures in an argon atmosphere. Wetting characteristics and possible interaction will be studied metallographically in the post-mortem condition. Complete results including metallographic examinations will be presented.

Jan 1, 1995

By Kimura. E.

Continuous estimation of phosphorus content of molten copper is required to produce phosphorus deoxidized copper in a continuous casting operation. The phosphorus content of molten copper was related to its electric resistivity, which was measured by the four-probed technique with a specially-shaped cell. In a laboratory scale, the linear relationship between the above factors was confirmed in the temperature range of 1083OC through 1200°C. The phosphorus concentration range measured was from 40 to 500 ppm. The phosphorus content was monitored successfully by measuring the electric resistivity of the molten copper in the distributor of a continuous caster in an industrial scale.

Jan 1, 1992

By K. Hussin

Perlis is one of the major producers of ?Batu Reput? in Malaysia and majority of the deposits contain of high-purity calcium and magnesium carbonate. The composition of Batu Reput is similar with the ordinary dolomite. Currently, the ?Batu Reput? is used as filler in the road construction, however with this new invention, it can be value added and maximized its application in the daily life, for example as construction materials, decorative products, souvenir and etc. This paper presents the fabrication of Artificial Marble from ?Batu Reput? and in this case, it was used as filler in the matrix of epoxy which is acted as a binder.

Jan 1, 2006

By M. H. Ghandehari

Sintered (Pr,Sm)Co5 displays a multi-phase microstructure in which closely related intermetallic compounds are formed during the process of fabricating useful magnets from over-stoichiornetric compositions. These compounds have much lower magnetic crystalline anisotropies compared to those of SmCo5 and PrCo5. Despite a careful control of the microstructure in producing "single phase" PrCo5 base magnets, sufficient concentrations of the lower anisotropy phases are formed which act as nucleation centers for domain reversal, resulting in a drop in coercivity. This article describes the use of sintering additives, primarily oxides, to prevent the formation of the magnetically soft phases in the final microstructure.

Jan 1, 1989

By R. Boom, Y. V. Meteleva-Fischer, B. Kraaijveld, H. Kuntzel

"Segregation of impurities during refining of metallurgical grade silicon (MG-Si) is an option to produce solar grade silicon (SG-Si). Directional solidification is a last step in production of SG-Si effective for removal of metallic impurities. The possibility is investigated to use metallic impurities originally present in MG-Si for removing boron and phosphorus. MG-Si has been treated using two methods: 1) alloying with calcium and 2) refining with Na2O-CaO-SiO2 slag, both by controlled cooling. The microstructure of silicon and the impurities distribution have been studied before and after the treatments. Using EPMA phosphorus and boron have been detected in 1-2 wt% concentration range in several intermetallic compounds in grain boundaries after both treatments. This observation points to a different possible mechanism of silicon refining from boron and phosphorus. Controlled cooling improves migration of phosphorus and boron to the silicide phases in grain boundaries, which can be removed by acid leaching treatment.2. IntroductionStandards for silicon solar cells and growing demand on “green” energy require economical and efficient route to the production of solar grade silicon. Refining of cheap metallurgical grade silicon is one of the promising options, where application of existing metallurgical approaches can result in cost-efficient production on industrial scale. Focus in refining is on impurities, which are most difficult to remove: B, P, Al, Ti, due to their large segregation coefficient in silicon and low vapour pressure [1]. Moreover, more environmentally friendly technology in comparison to the traditional Siemens process [2] will be in accordance with societal needs. Based on properties of common impurities in metallurgical grade silicon, alloying refining and slag refining are suggested as competitive techniques having potential effect on removal of impurities harmful for conversion of solar energy [3, 4]. Alloying with Ca followed by acid leaching was found to be effective for removal of Fe and Ti from silicon [5] and to enhance also removal of boron [6] and phosphorus [7, 8]. In the work of Inoue et al. [8] drastically increasing removal of phosphorus from silicon has been observed with an increase of Ca content and a thermodynamics-based explanation was provided. Since phosphorus has been found to condense in the secondary precipitate mainly composed of CaSi2, it can be removed together with iron and titanium by consecutive acid leaching treatment. Slag refining is one of the metallurgical methods proposed to be effective for refining of metallurgical grade silicon from boron [9, 10]. Slags with additions of the following oxides to silica have shown positive effect on removal of boron: CaO [11-13], Na2O [11,14]. Mechanism of slag refining from boron is based on oxidation of boron followed by its incorporation in the slag network [9,11]; the same mechanism is suggested for refining from phosphorus taking into account that oxides of boron and phosphorus are known as network-formers [15]."

Jan 1, 2012

By R. T. Seaman

Pressure oxidative treatment of whole ores and/or mineral concentrates is used to leach or liberate metals of value for downstream recovery. Silver, when present, is often lost in processing, precipitating as a cyanide-insoluble jarosite in the residue. Depending on pressure oxidation conditions, the degree of silver loss to jarosite can vary dramatically. Batch bench-scale testwork is often performed to define that loss, and then assess the implications in continuous operations. This paper focusses specifically on the impact of CESL pressure oxidation conditions on silver recovery, and discusses limitations of batch bench-scale testing as well as means of overcoming these limitations to better predict silver recovery in the scale up from bench-scale to continuous operations. Since silver is only partially soluble in both sulphate and chloride media, it will gradually leach and deport to a jarosite as oxidation progresses. When a silver-insoluble anion, for example iodide, is dosed prior to oxidation, there is a marked improvement in silver recovery from batchgenerated residue; however, that benefit is not consistently seen in continuous operations. The difference has been attributed to the dynamic solution conditions in the batch test, specifically the first few moments of oxidation. Using these principles, a predictive correlation has been established between initial leach concentrations of iron and acid and ultimate silver recovery with iodide addition.

By Andy Judge

"In traditional Permanent Magnet Machines, such as electric motors and generators, power is transmitted by magnetic flux passing through an air gap, which has a very low magnetic permeability, limiting performance. However, reducing the air gap through traditional means carries risks in manufacturing, with tight tolerances and associated costs, and reliability, with thermal and dynamic effects requiring adequate clearance. Using a magnetically permeable, high thermal conductivity material has the potential to improve magnetic performance, while at the same time offering performance advantages in heat transfer.Ferrofluids can be used to improve permeability in the rotor I stator gap. However, there are several tradeoffs in this approach. Fluid immersion comes with an increase in fluid friction loss compared to the windage losses of a traditional system. Isolating the rotating components from the ferrofluid can offset this effect. Also, while the magnetic effect can be positive for gap permeability, leakage flux can increase, and saturation can limit gains. These effects must be taken into account for a system optimized for ferrofluid immersion.IntroductionPermanent Magnet Machines (PMM's) convert electrical energy to mechanical energy in motor applications, or, for generator applications, convert mechanical energy to electrical energy through means of passing alternately polarized magnets past electrical coils. Looking at a simplified version of a PMM, where Rx is magnetic reluctance and <l>x is magnetic flux, we have the circuit shown in Figure 1."

Jan 1, 2013

By Shi Guan-Yong, Niu Li-Ping, Dou Zhi-He

"In the preset work, the viscosity model (named modified KTH model) proposed by Sichen Du and S. Seetharaman et al and extended by Shu Qi-feng was applied to the ESR slag systems. A correlation to predict the viscosities of CaF 2-(CaO)-Al203 slags using interaction coefficients of different cations in the presence of oz-and viscosity interaction coefficients between oz-and F in the presence of different cations has been developed. The interaction coefficient between oz- and F- in the presence of Al3+ was determined from the experimental data as shown in known literatures. The good agreement between the calculated viscosities and the experimental data in the CaF2-(CaO)-Al203 systems has indicated that this approach can be successfully employed to predict the viscosities of ESR slags.IntroductionReliable viscosities data of high-temperature slag melts are important for the modeling and design of high temperature metallurgical processes. Although a number of experimental measurements have been carried out, the available viscosities data is still scarce compared to the needs of today's technology, especially in the case of complex melts. In process simulations, the needs of viscosity descriptions for complex systems which could enable the extrapolation of the data as functions of temperature and composition is strongly felt today."

Jan 1, 2013

By K. S. Barros, D. C. R. Espinosa, J. A. S. Tenório

Over the past several decades, electrodialysis membranes have been employed for the removal of metals from galvanizing industry effluents. However, for its technical viability, it is useful to know some properties of the system to avoid, for example, precipitation of inorganic salts, destruction of the membrane and an increase in the energy consumption. The scope of the present study is to use chronopotentiometry to determine limiting current densities, transition times and resistances of the cationic membrane HDX 100 using a synthesized solution of the galvanizing industry effluent prepared with copper sulfate and sulfuric acid in different concentrations: 0.1, 0.5 and 1.0 g/L of Cu +2. The current-voltage and chronopotentiometric curves obtained have clearly defined regions and it was verified that the Cu+2 concentration causes a significant increase in the limiting current densities and in transition times. However, a high decrease in resistance occurred because at the highest concentrations, it is more difficult to reach the zero concentration value at the membrane surface. Besides, the pH increase causes a significant decrease in the limiting current density and in the transport number, but a slight increase in the resistance due to the presence of hydrogen. The results obtained confirm that the chronopotentiometry method is a valuable tool to determine membrane properties.

Mar 1, 2017

By James M. Lockwood

"Eureka Technology has developed and patented a technology for the recycling of EAFD. Through this process all constituents of the material become salable commodities or are returned to the steel making process. In transforming the EAFD ""waste"" stream into a ""process"" stream the Steelmaker eliminates potential liabilities and the uncertain future of current processes while further reinforcing its role as a recycler. This is a cost-effective and energy efficient technology that combines hydrometallurgic and electrolytic processes resulting in the recovery of salable metals. For instance, unlike pyrometallurgic processes, zinc is recovered in metallic form and no elements are volatilized. This on-site operation also eliminates expensive transportation costs. In summary this technology reduces the cost of dealing with EAFD by recycling material currently being landfilled.IntroductionWorld crude steel production reached a new record level in 2007 - 1.34 billion tons of which 31% was produced by EAF steel makers [1]. This resulted in the generation of over 6 million tons of EAFD. This steel byproduct contains significant amounts of lead, cadmium and other hazardous metals. In the United States the Environmental Protection Agency (EPA) has designated EAFD a hazardous waste (EPA waste code K061). With over 50% of steel production in the US coming from EAF steel making this byproduct represents the single largest source of solid hazardous waste generated."

Jan 1, 2008

By J. G. Reid

Nickel is second only to aluminium, of all non-ferrous metals, in energy required to convert the ore to metal. Nickel Laterite ores, which constitute the feed source for approximately 40% of world nickel production, are at a particular disadvantage because of the absence of sulphur, as an energy source, in the ore and because lateritic ores general 1 y are not amenable to beneficiation. The dramatic escalation of oil prices which commenced in 1973 and continued for a decade meant that Nickel Laterite refineries using oil as a primary energy source were placed at a distinct disadvantage relative to refineries utilizing nickel sulphide concentrate feeds. By the late 1970&apos;s the continuing large difference in oil and coal prices caused Greenvale to consider converting certain high oil consuming areas of the refinery to coal. These investigations confirmed that the areas of ore drying and power generation, which together consumed 50% of total Plant oil requirements, could be economically converted from oil to coal firing. Construction of the coal conversion facilities commenced in October 1980 and the first ore drying air heater came on line in August 1981. Construction was completed with the commissioning of the coal fired boiler in June 1982. This paper outlines the additions required to receive and utilize coal in ore drying and power generation and how the changeover was completed with minimal process disruption.

Jan 1, 1988

By I. A. Ibrahim

Ilmenite, in its natural form, is an inactive mineral from which the selective removal of iron is rather difficult. The reactivity of ilmenite. so that it can be leached with dilute hydrochloric acid, can be enhanced by chemical reduction in solution using a suitable metal as a reducing agent. The present paper aims at the evaluation of an Egyptian ilmenite ore for the production of synthetic rutile by direct leaching with hydrochloric acid in presence of iron powder. In this process, the titanium and iron contents are dissolved; meanwhile, the dissolved titanium is hydrolyzed and re-precipitated leaving mainly iron in solution. Leaching conditions were optimized to obtain less iron in the final solid product. Addition of sufficient amount of iron powder during leaching reduces the dissolved Fe3+ to Fe2+ and reduces the dissolved Ti4+ to Ti3+. The creation of Ti3+ in solution is assumed to have a role in dissolving the ferric iron and hence increasing the reactivity of the ilmenite ore. Synthetic rutile of about 90% TiO2 and 0.77% Fe2O3 was obtained from ore with a grain size 100% passing 200 mesh and a 5-hour leach time with 20% HCl at boiling temperature (110°C) and 0.11 g iron powder / g ore.

Jan 1, 2003

By J. Ipinza

The slime formation with several metallic impurities from acidic electrolytes of copper has been studied. On fresh Pb-Ca-Sn anode surface firstly the formation of PbSO4 takes place, then, it is transformed in the conducting PbO2, which covers the anode surface. It has been experimentally established the formation of a manganese dioxide double layer at the anode; this double layer was always composed of a thick external layer of non-adhering and easily removable scales, and of a thin internal layer, which adheres relatively well to the surface of the electrode. It was found that manganese dioxides present in the slime were of different nature: a non-adhering layer produced by electrolysis (-MnO2) on the PbO2 surface and a pure chemical precipitation in the solution (-MnO2). When iron is present in the electrolyte on this last layer of manganese, lead sulfate was found. In the case of arsenic and antimony in the electrolyte the slime generated was found to be lead sulfate and amorphous compounds of those ions. The lower slime generation in Chilean EW plants could be due to the lower contents of iron and manganese in the electrolytes. It was found that this slime formation rate not only is due to the electrolyte composition but also to the poor control of operational parameters at EW plants.

Jan 1, 2003

By Guozhu Ye

Hydrometallurgical zinc recovery from EAF dust has several advantages compared to pyrometallurgical alternatives in terms of low temperature operation, lower energy consumption and higher flexibility. Many hydrometallurgical processes have been suggested and tested over the years without success. The main reasons are: -Low leaching yield of zinc due to the fact that a high fraction of ZnO in the EAF dust exists in the zinc ferrite structure which makes selective leaching of ZnO not possible -Many of the proposals could not handle the halide in the EAF dust To eliminate these two disadvantages, two zinc ferrite elimination concepts have been tested and developed in the REZIN project of the EU 5th Framework Programme. The two concepts for zinc ferrite elimination could be shortly described by the following chemical reactions: A. ZnOFe2O3 + 2CaO = Ca2Fe2O5 + ZnOfree B. ZnOFe2O3 + C = Femet + CO/CO2 + ZnOfree These two concepts were investigated in details in combination with a subsequent leaching step using the novel EZINC process for recovery of zinc from EAF dust. Leaching of pretreated samples has shown great increases of a zinc recovery yield. A zinc recovery of over 90 % could be reached, as compared to about 50 % for no-pretreated samples. This paper will describe the two concepts in details.

Jan 1, 2006