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By Shadia J. Ikhmayies

"Nanocrystalline CdS thin films were prepared by vacuum evaporation on glass substrates at ambient temperature. The films were characterized by recording and analyzing their transmittance, X-ray diffraction (XRD) patterns, scanning electron microscope (SEM) images and Energy dispersive X-ray (EDAX) spectra. X-ray diffractograms revealed that the material is nanocrystalline with predominant cubic crystal structure and preferential orientation along (1 1 1) plane. SEM micrographs confirmed the nanostructure of the material and showed uniform and well covered surfaces. EDAX reports revealed that the films are cadmium rich and contain oxygen. The first derivative of the absorbance was used to estimate the effective bandgap energies of the nanocrystallites and the hyperbolic band model was used to estimate their radii. The results were compared with those obtained by XRD and SEM measurements.IntroductionCdS thin films are of considerable interest as they can be used in fabrication of solar cells and other opto-electronic devices. In particular, heterojunction solar cells with a narrow band gap base and wide band gap window have been investigated in an attempt to develop efficient, stable and low-cost solar cells [1]. The CdS quantum dot embedded in a glass matrix is one of the well-known quantum dot systems and its electronic and luminescent properties have been studied extensively [2].Three-dimensional confinement of carriers within the quantum dots leads to the blue shift of the optical band-gap and to modification of many properties of semiconductor material [3]. It has been argued that in these semiconductor nanoparticles the hyperbolic band model gives a better fit to the observed quantum size effect as compared to the effective mass approximation [4]."

Jan 1, 2012

By Ditze A., C. Scharf

Magnesium type 1 - scrap can be remelted without flux in the presence of different sulfur containing protective gases. Beside the draw back in the use of these gases, that either are contributing to the global warming potential (SF6) or are poisonous (S02), residues like dross and crucible sludge are produced. Dross and sludge now a days must be utilized. Partly these byproducts can be used in the aluminum industry and partly for desulphurisation of hot metal and steel. Another possibility is melting of dross and sludge with flux for the production of a secondary magnesium alloy. Then again residues are generated that must be processed. Therefore, the whole material cycle has to be considered to decide which kind of utilization practice is optimum. Based on experiments this question is discussed and the material balances for fluxfree melting, melting with flux and fluxfree melting plus other utilization of the residues are presented.

Jan 1, 2000

By C. A. Nogueira, F. Pedrosa, F. Margarido, R. N. G. Guerra

"A hydrometallurgical process for recycling spent Zn-MnO2 batteries was developed, involving leaching with sulfuric acid, purification by precipitation and metals separation for further recovery. Leaching of zinc oxide was easily attained while for manganese oxide was rather difficult depending on temperature and acid concentration. At 90°C and with the liquid/solid ratio of 20 L/kg, more than 95% of zinc is recovered in 30 minutes with 0.5M H2SO4. To attain similar recovery for manganese, higher levels of acid concentration and time are needed (e.g 0.7 M and 2 hours). After leaching a purification step is necessary to remove iron co-dissolved through Fe(III) precipitation. Separation of zinc from manganese by solvent extraction with 1M DEHPA follows in the process route. The countercurrent multistage separation diagram developed allows the production of a zinc electrolyte with 120 g/L Zn and 0.005 g/L Mn, and a raffinate with 16 g/L Mn and 0.013 g/L Zn.IntroductionThe recycling of spent Zn-MnO2 batteries is carried out by dedicated recyclers using several process alternatives [1]. Most of the running processes use pyrometallurgical technologies [2] based on zinc distillation. Alternative treatments by hydrometallurgy have been reported [3-5] but its application is scarce.In order to contribute to the development of alternative solutions, a process for recycling batteries based on Zn-MnO2 systems has been studied. The process is based on the hydrometallurgical treatment of spent batteries in sulfuric acid media (Figure 1). The process starts with the physical processing by shredding using cutting grinders, where the batteries are opened and size reduced, allowing the liberation of the interior electrode particles or pastes. The fines can be then separated and the coarse material containing the steel scrap can be treated to remove the remaining aggregate electrode. The final scrap also contains some plastics and other non-metal materials and can be further valorized."

Jan 1, 2008

By V. G. Papangelakis

The implementation of a flow-through yttria-stabilized zirconia (YSZ) sensor for pH measurements in high temperature and concentrated electrolyte systems relevant to hydrometallurgical processing of nickeliferous laterites is discussed. Instrumentation involved the use of a custom made flow-through titanium electrochemical cell. Accuracy and validity of the pH measurements at temperatures up to 250C were assessed using concentrated sulphate process solutions ranging from synthetic binary sulphuric acid ? water solutions to progressively multicomponent metal ? sulphate solutions simulating laterite Pressure Acid Leach conditions. The measurements were also compared with theoretical models using recently obtained thermodynamic data. A difference of ±0.25 pH units was observed between measured and calculated pH values at temperatures. This is an acceptable difference given that these are the first direct high temperature pH measurements ever on the concentrated acidic sulphate solutions. This result is encouraging more research for the development of industrial electrochemical systems for direct pH measurements in autoclaves.

Jan 1, 2003

By Yong Zhao, Yan-hui Sun

Behaviors and evolutions of MgO·Al2O3 in non-oriented silicon steel during calcium treatment were investigated by thermodynamic calculations and high-temperature experiments. MgO·Al2O3 inclusions were the main type of inclusions before calcium treatment, which is also confirmed by the stability diagram of MgO/MgO·Al2O3/Al2O3 from thermodynamic calculations. After calcium treatment, the majority of original MgO·Al2O3 inclusions were mainly modified to CaO-MgO-Al2O3 system inclusions, this would be beneficial to improve castability and product quality of silicon steel. But there was no modification happening to some MgO·Al2O3 spinels which were directly surrounded by CaS inclusions. The content of Al2O3 occasionally existed a sudden increase besides a common decrease in the product layer of CaO·MgO·Al2O3. Then the evolution mechanisms of MgO·Al2O3 inclusions were proposed in present work. Thus, Al/Mg atom ratio had a significant influence on the modification of MgO·Al2O3 spinel.

Jan 1, 2016

By G. G. Barbante

Copper anode slimes are a valuable source of the precious metals, and selenium and tellurium. They are mineralogically complex and this has led to a great variety of process flowsheets for treating them. The traditional pyrometallurgical method utilises oxidation in a reverberatory furnace, but has numerous shortcomings. Recently deep-bath intensive smelting methods have been developed for use in the larger refineries. Despite these process advances, the thermodynamics of the reactions involved remains poorly understood. An initial description of the thermodynamics of slimes smelting is presented, but is severely limited by a lack of basic data. It is shown that slimes smelting is superficially similar to copper converting, but has many unique features. More basic thermodynamic data on selenium-based systems are needed before the process model presented can be further refined, and work in this direction has already commenced.

Jan 1, 1994

By J. N. Hryn, E. J. Daniels, M. Askew, Kirchner. G.

This presentation addresses the changing regulatory climate towards aluminum dross and salt cake in Europe and in the United States. Although sporadic, the trend in the U.S. continues to be away from command-and-control regulation of these materials. This trend began in the early 1980s when the Environmental Protection Agency was successfully sued in court and prevented from classifying dross as a hazardous material. The situation in Europe is different. Because of Council Directive 96/61/EC from the European Commission, European Union member countries have all passed legislation that will essentially cause all salt cake and drosses to be reprocessed. The implementation date of the legislation varies from country to country: from 2001 in the United Kingdom to 2007 in Germany, France, Austria, Italy, and Spain. The European aluminum industry is urging the EC to use the approach adopted by the U.S. EPA, which declassifies the majority of aluminum drosses and salt cakes.

Jan 1, 2000

By P. T. Velu

Light weight aluminum alloys are the major construction materials for a number of structures in automobile and aerospace industries. Higher cost of production is the key impediment which restricts the usage of these alloys. A new electrochemical process route for the low cost production of aluminum alloys is being investigated, in which alloying elements are obtained from the dissolved compound. In the present investigation, solubility of lithium compound has been determined by measuring the EMF, when it is dissolved in the electrolyte. The solubility of Li2CO3 increased with temperature from 2.95 wt pct at 1063 K to 7.57 wt pct at 1093 K. Activities of the compound in the electrolyte were deduced using Temkin's ideal solution approach.

Jan 1, 1995

By Vinay Kumar, Jae-Chun Lee, Abhishek Kumar, Manis Kumar Jha

However, India is rich in ores and mineral, but E-waste recycling is necessary due to the report of national and international studies, which cautioned on the generation, treatment and accumulation of e-waste in India. Current data indicate that the total domestic e-waste generation including imports is around 382979 MT, however waste available for recycling and actually recycled are 144143 MT and 19000 MT, respectively. In which recycling by non-formal and formal sector are 95% and 5%, respectively. On the other hand, India has developed expertise in handling verities of metallic wastes in an organized and safe manner. The development of individual process or combined processes for handling the e-waste is underway. Eco- friendly and energy-saving processes are necessary to comply with stringent environmental regulations. The paper includes the recent trend of e-waste generation, recycling process and its future prospects particularly in India.

Jan 1, 2011

By Z. S. Wronski

In rapidly solidified Fe-Nd-B permanent magnet alloys, the content and distribution of Nd-rich intermetallic and Fe-phases determine coercivity Hc and remanence Br. Consequently, microstructure plays a crucial role in deter- mining the (BH) max-product of permanent magnets fabricated from these alloys. A study has been initiated to investigate changes in microstructure and the effects on magnetic properties as the material is processed from arc-melted ingot to melt-spun flakes and finally to a product consolidated by hot-forming. Anisotropic magnetization behaviour has been observed in rapidly solidified flakes after low-temperature annealing.

Jan 1, 1989

By C. A. Morais

The present work describes the development of an efficient and relatively simple process to obtain high grade CeO2 from a mixed rare earth chloride solution. The process involves cerium oxidation and precipitation by addition of a KMnO4-NaCO3 solution. The experiments were carried out at room temperature (25 1° C). The results indicated that the major parameters affecting cerium recovery are the molar ratio of KMnO4/Ce, the initial acidity of the chloride feed solution and final pH of Ce(OH)4 precipitation. In strong acid solutions (pH < 1), the oxidation of Cl to Clo took place in addition to the oxidation of Ce(III) to Ce(IV), so increasing the permanganate consumption. Conversely, low acidity (pH >3) led to coprecipitation of the other rare earth elements. Under the selected conditions, cerium was selectively precipitated as ceric hydroxide, together with some manganese dioxide. Further purification was carried out by the dissolution of Ce(OH)4 in HCl, followed by precipitation as cerium carbonate. The filtrate was neutralised with a Na2CO3 solution in order to recover the associated rare earth elements for further separation. The final product, assaying 99.7 % CeO2, was obtained with a recovery of nearly 100%.

Jan 1, 2003

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 F. J. Tavera

A study on the electro kinetics of lead carbonate, silica, and alumina, in aqueous media was carried out at different pH values. The behavior of potential was determined for these species in the pH range between 3 and 12. Homocoagulation of lead carbonate in aqueous media is analyzed at its isoelectrical point. Lead carbonate heterocoagulation is analyzed with silica, alumina, and silica ? alumina mixtures at low pH values. The experimental results are considered for their possible application to treat residual water polluted with lead.

Jan 1, 2006

By Daniel Helm

The first industrial application of direct solvent extraction of nickel from hypersaline sulfate feed solutions has highlighted the need to investigate the influence of chloride on the extraction behaviour nickel in the presence of calcium using Versatic 10 and the solubility characteristics of gypsum. Temperature-solubility curves for gypsum in various aqueous electrolytes were prepared. The solubility of gypsum is increased significantly by the presence of sulfate ions, while chloride ions decrease it for a given temperature. The anion effects of chloride and sulfate on the extraction of calcium and nickel by Versatic 10 corresponded well with the complexing ability of the anions. It was shown that the presence of chloride shifts the extraction isotherms for both metals significantly to the left, while decreasing the selectivity of Versatic 10 for nickel over calcium. The loading of nickel onto Versatic 10 in this system was shown to be at a maximum within 3 seconds, while calcium extraction took between 4 ? 5 seconds to load to a maximum. Chloride ions had no influence on loading kinetics of nickel, but depressed the rate of calcium loading. It was shown that in the presence of an excess of nickel, calcium loading is effectively eliminated, and that calcium is scrubbed from Versatic 10 within 2.5 seconds of contact with nickel electrolyte.

Jan 1, 2003

By Robert Kozicki, Eric Graham, George Wrightson

"IntroductionThe manufacture of Ferro Chromium involves the smelting of various ores and fluxes to produce the metallic product.Slag is inherent in the process. It has a much lower density than the metallic FeCr. Some chrome may be trapped in the slag as either FeCr or Cr203.Previous methods to estimate the slag in the FeCr have revolved around separating the slag and metallic portions by exploiting the differences in density. The downside with that procedure is that material will often contain pieces that are adhered FeCr and slag. The Metallic FeCr may also be completely encapsulated in the slag.An alternative and more precise method involves calculating the slag content based on chemical analysis of Mg and Al. The Mg and Al will be at relatively low levels (less than 0.1 % ) in the Metallic FeCr pieces and considerably higher in the slag (3% or greater). The overall sample will have a proportional amount and is calculated using simultaneous equations with the assumption there is only one kind of slag and one kind ofFeCr present. ""Pure"" slag and ""pure"" FeCr are needed in order to determine the Mg and Al in each. The detemlination of the Mg and Al in the overall sample would then be used to calculate the amount of slag.When the particle size is small, it is difficult to sample and get ""pure"" pieces of the slag and FeCr of sufficient quantity to perform a proper analysis. Often, historic data is used but that is dependent on the source of the FeCr and the materials used in its production. Mg and Al levels in slag can vary between 3% and 20% in different FeCr slags depending on their origin."

Jan 1, 2013

By I. D. Reznik

On blowing nickel matte in a converter without quartz, first the oxidation of metallic iron and a part of FeS occurs without evolving sulfur dioxide, the formed FeO dissolves in a sulphide smelt and form a homogeneous oxysulphide smelt. On further increasing the FeO content, the oxysulphide separates into 2 layers. Based on the laboratory investigation of FeO-(FeS+Fe°) - (Ni3S2+Ni°) ternary phase diagram we have identified the separation region at 1250°C. The boundaries of the separation region have the form of an arc and the composition of the separated oxysulphide layers is defined by the canodes. In the nickel or copper-nickel matte - silicacalcium oxide slag system at 1250°C three layers, namely sulphide, oxysulphide, and slag may be formed. A high slag basicity due to the presence of CaO can serve to enhance the activity of FeO; a low nickel content in the matte corresponds to a high concentration of FeS therein; FeO from slag and FeS from the matte form a homogeneous FeO-FeS solution, i.e. an oxysulphide layer. The investigation on the "Camebaks" apparatus and by the nuclear gamma-ray resonance spectroscopy method of the phase composition in a slowly cooled oxysulphide layer has shown the presence of four phases: wustite, troilite, ferronickel grains, and calcium oxide-silica inclusions. Knowledge of regularities in the oxysulphides formation makes it possible to use them in pyrometallurgy of nickel and cobalt or preventing their formation.

Jan 1, 1997

By A. F. Sidorov

A method of improving mineral recoveries from ores by modifying the physical and chemical properties of minerals using radioisotope radiation was tested. It was observed that irradiation modifies mineral cell sizes, changes the crystal structure of some minerals, reduces the sulfur content 1 to 1.5 % in sulfides, changes the zeta potential, alters the surface properties of mineral grains I and produces other changes. Preliminary tests indicate that accelerated electron treatment of ores in connection with mineral processing has a potential for improving mineral recoveries by flotation and by magnetic separations.

Jan 1, 1989

By M. Olper

Today, copper production from direct leaching of oxidized copper ores followed by solvent extraction-electrowinning (SX-EW) accounts for about 15% of the total primary world output. SX-EW is a well-accepted process with an operating cost in the range 16-20 cents/lb. copper for small and medium size plants, depending on the plant size and local conditions. However, this technology presents some drawbacks that affect the operating cost and cause environmental concerns. ENGITEC and Paques Bio Systems have developed a new process that avoids the solvent extraction step and operates the copper electrowinning step at a lower cell voltage because of the depassivation of the anodic reaction. The consequence of this new concept is that the direct operating cost is in the range 10-12 cents/lb. copper. This new process is composed of the following steps: ? Selective precipitation of copper from leach solutions by biogenic H2S, yielding CuS and regenerating acid ? Leaching of the CuS with a ferric fluoborate solution to dissolve copper and produce elemental sulphur that is recycled back to the H2S biogeneration step ? Electrowinning of copper fluoborate solution in a diaphragm cell with the ECUPREX® Process, producing copper cathodes and regenerating the ferric fluoborate solution to be recycled back to the leaching step ? Biogeneration of H2S from the elemental: sulphur generated during the leaching step, with the nutrient source for the anaerobic bacteria selected form a wide range of organic substances and/or some industrial by-products containing carbon and hydrogen This paper describes all process steps with particular reference to the biological H2S generation technology. Also discussed&apos; is the capability of the ECUPREX® Process to treat copper sulphide concentrates and copper matte.

Jan 1, 1999

By E. J. Peuraniemi

Recently commissioned Kennecott-Outokumpu flash converting was developed to replace the approved but environmentally outdated Peirce-Smith -converting to satisfy the globally tightening emission regulations. In the present study, dust formation and reaction mechanisms of two copper mattes with different experimental parameters were studied in lean suspension conditions. Both mattes had very high copper content of approximately 75 wt% and low iron content of 4.5 wt% and 1.2 wt% Fe. A laboratory scale, vertical laminar-flow furnace with a low feeding rate was used to simulate the phenomena taking place in the reaction shaft of a flash converter. Experimental conditions included temperature of 1300 °C with reaction gas oxygen contents of 20 vol%, 50 vol%, and 75 vol%. In the experiments, sieved particle fractions were fed to the furnace and sampled after short reaction time intervals by quenching them into a water film. Collected particles were analysed chemically for their main elements to define their removal rates. Also, optical and scanning electron microscopy with EDS-analyser were applied to determine phenomena occurring during reactions. Kinetics of oxidation as well as ignition of particles are discussed. Changes in particle morphology, size, and composition are reviewed to describe dust formation and reaction mechanisms.

Jan 1, 1999

By David Hughes

The paper covers the utilization of on-line analysis in process control of solvent extraction in nickel leach solvent extraction processes in Finland and Australia and in copper heap-leach and solvent extraction in Chile. The goals of and requirements for controlling the solvent extraction stages of the processes are reviewed. The applications at three plants are compared. The development of the technology used is reviewed and design considerations are discussed. Requirements for on-line control and analyzer performance are compared. A new generation of analyzers and its effect on the set-up process of a project is introduced.

Jan 1, 2003