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By Guo Xueyi

The nonferrous metal industry is facing the resource depletion, energy crisis and environmental deterioration. The resource recycling is a correct way to promote the nonferrous metal industry development towards sustainable. To realize the resource recycling, the technical support is most important. In this paper, the techniques barrier for nonferrous metal resource recycling are summarized, the fundamental on resource recycling of nonferrous metals are proposed.

Jan 1, 2006

By J. C. Agarwal

Rare earth metal alloys are becoming increasingly important, particularly those of neodymium, because of their magnetic properties. This paper will present a generalized approach to the production economics of the metallic rare earth alloys. With appropriate regard for the chemistry of different rare earths and the large impact of economies of scale, it is possible to make fairly accurate estimates of the production costs of other rare earth alloys as well.

Jan 1, 1989

By Takashi Nakamura, Kenji Oosumi, Kazuhisa Fujisawa, Takayuki Kogishi

"Recycling of used aluminum beverage cans(UBCs) is one of the important issues for aluminum manufacturer presently. The direct re-melting of UBCs shows two problems. One is a reduction in molten aluminum recovery and the other is a contamination of other metals such as Ti and Fe from paints. Both problems are caused by paints coated on the surfaces of aluminum cans. Removal technique of the paints, therefore, has been required. Although roasting and shot blast techniques have been developed, both were not successful in removing the paints effectively. A swell-peeling method has been applied to remove them using a methylene chloride solution with acids and it works very well. Small laboratory scale tests have been carried out to develop the commercial process and clarify the mechanism of the swell-peeling method in the present study.When the surface area of UBC is more than 10 cm2, peeling time is independent of the surface area, about 60 seconds, because swelling phenomenon is controlled by the penetration of the liquid through the fine pits on the surface of the paint. This is good for a commercial process. Peeling takes place when the swelling force generated by methylene chloride exceeds the adhesion force between the film and the surface of aluminum, that is weakened by the coexisting acid, especially halogenated acetic acid."

Jan 1, 2000

By T. V. Jayaraman, D. Das, B. Mallesham, A. R. James

The PNN-PZT xPb(Ni0.3Nb0.67)03-(1-x)Pb(Zr0.31 Ti0 69)03 (0.2=x=0.6) based relaxor-ferroelectric material was synthesized by colurnbite precursor (NiNb206) method via conventional solid state reaction. Homogeneous mixture of required oxides and precursor was calcined at 850°C for 4 hrs to obtain phase pure perovskite. Pellets of PNN-PZT ceramics were sintered at 1100oC for 4 hrs. Phase pure perovskite structure was confirmed by the X-ray diffraction analysis. From the X-ray diffraction analysis it is also confirmed that there is a structural transformation from the rhombohedral to tetragonal with increase in PZT content and existence of morphotrophic phase boundary (MPB) at x = 0.5 composition. The morphology and microstructure of the sintered pellets were observed using the scanning electron microscope. P-E loop measurement shows the high remnant polarization (19.12 µC/cm2) and low coercive field (6.89 kV/cm) at MPB compared to all other compositions. The electromechanical planar coupling coefficient (kp) was measured through the resonance and anti-resonance method using the LCR meter. The piezoelectric strain coefficient (d33) measured directly using the d33-meter. At x = 0.5 composition the highest value of d33 = 398 pC/N is obtained.

Jan 1, 2012

By Jakub Kaczorowski

In the production of Mn-alloys, the Boudouard reaction significantly influences the mass and energy balance. The endothermic nature of this reaction requires more energy for the process, while the direct consumption of carbon is reflected in the greater demand for carbonaceous raw materials. Therefore, it is desirable to eliminate or suppress the reaction. The kinetics of the Boudouard reaction are a function of many factors, of which coke properties and the conditions around the particles (i.e. temperature, gas composition) seem to be the most important. In the present study properties of selected single source and commercial metallurgical cokes are compared with reactivity results. The single source cokes represent a single coal that has been carbonized in a laboratory scale furnace. The commercial cokes are products of carbonization of coal blends under industrial conditions. The coke properties include proximate, ultimate and ash analysis. Also, coke petrography with carbon forms is included. The reactivity tests were performed on different particle sizes at various temperatures, gas compositions and gas flow rates. The experimental parameters were chosen to simulate the conditions in an industrial furnace. The results show that highly graphitized structure of cokes, minimal surface area and a low concentration of ash retard the reactivity. Of the other factors, the temperature and the gas composition have the greatest impact on the reactivity.

Jan 1, 2006

By Richard Krentz

Two separate on-line analyzers are operated at the Corefco metals refinery. The first application is an on-line refractometer which measures the ammonium sulphate concentration in the primary feed slurry tank. The second application is a multi-stream X-Ray fluorescence analyzer which measures the metals and sulphur concentrations in eight key refinery streams. Specific applications of the on-line analyzers with advanced control systems for improved process control will be discussed.

Jan 1, 2003

By Tugba Basargan Çagatay Morall, Gülhayat Nasun-Saygili

"The aim of this study is to prepare the apatitic material using colemanite mineral (2CaO.3B2O3.5H2O) which was obtained from Eastern Anatolia, Turkey. For this purpose, colemanite mineral was reacted with different phosphate sources, namely, dipotassiumhydrogen phosphate, ammoniumhydrogen phosphate and ortophosphoric acid at various temperatures and time periods. Experiments were run in batch system. The apatitic material was prepared by a wet method and followed by heat treatment at various temperatures. Structure of the samples was analyzed by XRD, FTIR, XRF and SEM. The particle size analysis was also made for the result product. The experiments showed that reaction temperature, contact time and heating temperature are important parameters to transform the colemanite into apatitic structure. Reaction of colemanite with dipotassiumhydrogen phosphate and ammoniumhydrogen phosphate results in amorphous, non-stoichiometric hydroxyapatite type structure, while acid based phosphate source gives brushite and monetite type product before and after heat treatment, respectively.IntroductionBoron which has properties intermediate between metals and non-metals is a member of semiconductor group of elements. Its atom is very small and has three valence electrons. Boron exists in Earth's crust (from 5 mg/kg in basalts to 100 mg/kg in shale) and in the oceans (4.5 mg/l) [1]. Turkey has 60% of world's boron reserves which is mostly in the form of colemanite (2Ca0.3B203.5H20). Colemanite is the most important calcium containing commercial borate mineral with 5 mol of crystal water [2].Calcium phosphate cements are very useful for bone repair applications because of its chemical structure. They are injectable, easy to shape and can be maintained locally. Because of those reasons calcium phosphate cements are very effective to fill bone defects with an irregular shape [3]. Hydroxyapatite (Ca10(PO)6(OHh) is the major component of the bone (70 wt%). However, hydroxyapatite stoichiometry, composition and crystallinity differ in human skeleton system [4, 5].The main objective of the present work was to study the transformation of colemanite to apatitic material using different phosphate solutions at several time spans and temperatures. The experiments were run in a batch system, change in pH and also weight loss were measured after the experiments. Several analysis methods were used to investigate the chemical and structural changes."

Jan 1, 2012

By Cheng Gong-jin, Chu Man-sheng, Liu Zheng-gen, Zhang Yong, Liu Jian-xing, Xue Xiang-xin

"High chromium vanadium-titanium magnetite is one kind of Fe-V-Ti-Cr composite ore resources, which owes high utilization value. Owing to lacking systematic study on the sintering of this ore home and abroad, effects of carbon addition and basicity on sintering process and sinter metallurgical properties, such as sinter yield, vertical sintering speed, tumbler strength, sinter machine utilization coefficient, and low temperature reduction degradation were investigated systematically under laboratory conditions in the paper. The results shows that, when high chromium vanadium-titanium magnetite proportion is kept unchanged as 13% in sintering feeds, sintering process index and metallurgical properties are the optimum under carbon addition 5.0% and basicity 2.70, which meets the requirements of blast furnace burdens. This research provides technical parameters for practical sintering production of high chromium vanadium-titanium magnetite.IntroductionHigh chromium vanadium-titanium magnetite (hereinafter abbreviated as hi§h-Cr V-Ti magnetite), in which Fe is closely symbiotic with Ti and isomorphous with V and Cr1'- l, is one kind of typical vanadium-titanium magnetite resources with high comprehensive utilization value but the difficulties are extremely high due to complex chemical composition and mineral structure. At present, the feasible and mainstream utilization process of high-Cr V-Ti magnetite should be the route of agglomeration-blast furnace smelting. Thus, sintering production is the foundation for high-Cr V-Ti magnetite utilization. However, till now there are few research documentations on high-Cr V-Ti magnetite sintering home and abroad. Under the above background, this study focused on detailed researches of high-Cr V-Ti magnetite sintering. Sintering process uses the powders or fine iron ores to produce artificial rich ore with good metallurgical properties 4l Solid fuel provides 90% heat requirement during sintering15J. The appropriate amount of fuel and flux should be added during sintering in order to provide necessary heat and maintain the desired basicity16l. That is to say, carbon addition and basicity are two key factors affecting metallurgical properties of sintering products17J. Therefore, the effects of carbon addition and basicity on sintering process and metallurgical properties, including sinter yield, vertical sintering speed, tumbler strength, sinter machine utilization coefficient, and low temperature reduction degradation, are systemically investigated under laboratory conditions in the study, on purpose to achieve the optimization of sintering process for high-Cr V-Ti magnetite."

Jan 1, 2013

By T. J. A. Smith

This paper provides an overview of some of the key issues in design of smelter gas handling systems, with particular reference to sulphide smelting plants. In both primary smelting and converting. gas handling and treatment systems often represent the major capital cost component. There is also ample evidence that poor system design can be a major cause of smelter down time, lost production and unforeseen high maintenance costs. The paper discusses these issues and offers guidance for improved design.

Jan 1, 1992

By Edouard Asselin, Guikuan Yue

"In the present study, electrochemical measurements, especially cathodic potentiodynamic polarization (CPC) and cyclic potentiodynamic polarization (CPP), have been employed to study the kinetics of ferric reduction on chalcopyrite in aqueous Fe( II )-Fe(III)-H2S04 solution at 25°C and 70 °C. Results from the calculation ofspeciation in the above solution reveal that, at both 25 °C and 70 °C, the real Fe3+/Fe2+ ratio is much lower than the nominal ratio, which leads to smaller values for the reversible potential of the ferric/ferrous couple based on the Nemst equation. Exchange current densities of the ferric/ferrous couple were obtained by extrapolating the cathodic linear Tafel line to the reversible potential and are on the order of 10-7·10-6 A/cm2 at 25°C and 10·6-10-5 A/cm2 at 70 °C, respectively. The transfer coefficients were about 0.35-0.38 at 25°C and 0.35-0.45 at 70 °C. Polarization plots of CPC and CPP under different nominal Fe3+/Fe2+ ratios are in good agreement at 25 ·c and at 70 °C. Based on the obtained exchange current densities, the rate constant k, was calculated and is on the order of 10-1 cm/s at 25 °C and 10 1 cm/s at 70 °C.IntroductionChalcopyrite is the most abundant copper mineral in nature, accounting for about 70% of copper reserves in the world [I]. In recent years, the metallurgical industry has been searching for a hydrometallurgical process as an alternative to pyrometallurgical treatment due to high emissions of S02 and capital costs associated with smelting. Activity in this area has increased recently due to some inherent advantages associated with hydrometallurgical processing, such as the possibility of treating low-grade ores (increasingly more abundant in the case of copper) and easier control of waste, with the attendant benefits to the environment [I]. Chalcopyrite is highly refractory under most hydrometallurgical conditions, owing to the formation of an anodic passivation layer on the chalcopyrite surface which renders the process kinetics very slow. Most of the currently proposed processes are based on sulfuric acid with ferric ions and/or dissolved oxygen as oxidants. Sulfuric acid is preferred over all other leaching reagents in terms of cost, environmental friendliness, and ease of its regeneration during electro-winning. Some of these processes have been piloted in attempts to implement these technologies on an industrial scale,"

Jan 1, 2012

By A. C. Cascalheira, L. M. Abrantes, M. Savic

This paper reports our results on the application of a novel process for the spontaneous and sustained reduction and recovery of elemental silver and gold on an electroactive polymer surface. This work incorporates the metal recovery from photographic films (silver) and goldsmith residues (gold), by direct contact of metal containing solutions with polymer. The performance on such process of electrochemically and chemically prepared polyaniline (P ANI) is evaluated. SEM coupled with EDX and XRD analyses confirmed the presence of metallic silver and gold deposited onto polymeric material.

Jan 1, 2000

By J. F. Elliott

The thermodynamic behavior of sulfur and oxygen in copper matte has been measured by equilibration of the melt 00 a gas consisting of CO, SO2 and Ar. The oxygen potential ranges from 10-9 to 10-7 and that for sulfur from 10-4 to 10-2 atm. The work is a continuation of the earlier study by Luraschi and Elliott in our laboratory. A model has been developed that permits extra-polation of the results to ascertain compositions of the matte that are saturated with various oxides of iron.

Jan 1, 1983

By Leah Penner, Thomas J. Ruth, Paul Schaffer, François Benard, Edouard Asselin, Stefan K. Zeisler, Thomas J. Morley

"This paper details the electrodeposition of metallic molybdenum from an aqueous, acetateelectrolyte containing molybdate ions. The deposition is carried out in a highly concentrated (up to I 0 M) acetate bath in the presence of a very low concentration of bone glue (60 µg/L). The molybdenum metal deposits are up to 20 µm thick and adherent. The deposits were characterized by XRD and XPS analysis. The deposition process is very inefficient, as up to 99% of the current is used to generate hydrogen during electrolysis. The effect of acetate concentration, pH, additives and current on the deposition efficiency and physical properties of the molybdenum deposit were investigated and optimized to obtain smooth, adherent coatings.IntroductionMolybdenum has increased thermal and wear resistance properties that are often utilized in material coatings [I]. These coatings are most often manufactured by sintering, pressing or spraying molybdenum powder at elevated temperatures, as a substitute method for standard metallurgical practices, such as electroplating [2, 3]. The lack of reports describing molybdenum deposition is most likely due to the highly oxophilic nature of molybdenum and the stability of its oxides, especially in water. Previous attempts to electrochemically reduce molybdenum from molybdate (Mool·) ions to molybdenum metal have reported the production of either a poorly adherent mixed oxide [4-6], or a thin(< 0.1 µm) metallic film [7-9]. Thick metallic molybdenum is capable of being co-deposited with one of the iron-group metals (Ni [10], Co [11] and Fe [12]) to produce an alloy [13, 14]. These alloys, however, may not be suitable for applications requiring pure molybdenum as they usually contain less than 50% molybdenum (often less than 30%)."

Jan 1, 2012

By A. I. Okunev

The investigation results are submitted on separation into layers in the systems Cu (Ni) - Fe - Ca - 0 - S - (Si), as well as on physico-chemical properties of oxide - ferrite, oxide-sulfide melts (density, surface tention, viscosity, electric conductivity), on kinetics and oxidation macromechanism of iron and sulfur in the oxide-silicate, oxide-ferrite and oxide-sulfide melts, kinetics of reduction of oxide-silicate and oxide-ferrite systems. Conditions are discussed for copper, nickel and zinc recovery from oxide-silicate and oxide-ferrite slag in liquid and solid states. Some promising technique is the technique of future, as is considered.

Jan 1, 1988

A rotating-discelectrode system was used to evaluate the electrochemical behaviour of Eu(III) during its reduction in NaCl solutions. The solution pH and NaCl concentration have a great effect on the reduction kinetics. The thermodynamic modelling study also revealed that Eu(III) exists in various forms in NaCl solutions. At a low concentration of NaCl, the predominant species is the free Eu3+. Other Eu-chloro complexes become more predominant when the NaCl concentration increases.

Jan 1, 1992

By C. Hecker, J. A. Garcia

To determine the kinetic reaction mechanism, electrochemical experimental techniques of stationary polarization, linear voltammetry and faradaic impedance were used. Gold electrodeposition experiments were realized using an electrolysis cell, provided· by a rotary disk of vitreous carbon and or' platinum counter electrode of platinum mesh and reference electrode. Using an automatic measurement system voltarnmograrns and Nyquist faradaic impedance spectra were obtained. In this paper, responses for different cases were analyzed through faradaic impedance criteria, considering several kinds of diagrams obtained. The importance diffusion influence of aurocyanide ions and adsorption as controlling steps previous charge transfer was verified. A model of proposed mechanism is discussed.

Jan 1, 1997

By James P. Bennen

Limited efforts have been made to recycle/reuse-spent refractory materials in the steel and aluminum industries of North America. The driving force is usually part of a larger waste reduction program. -Economic or legislative forces have not been a driving force for spent refractory recycling/reuse. Past and current spent refractory recycling / reuse practices will be reviewed, with emphasis on specific programs at steel and aluminum companies. Program goals and progress of the joint Office of Industrial Technologies-DOE/Steel Manufacturers Association program directed at spent refractory reuse with electric arc furnace steel producers will also be discussed.

Jan 1, 2000

By Khoo Khyou Pin, Yoshiyuki Funaki, Hirotsugu Takeuchi, Ryoichi Urao, Naotatsu Asahi

"Steel is used to be ion carburized with mixing gas of methane and hydrogen. In carburizing, carbon in the methane decomposes and deposits on the steel by plasma, so methane gas flow may influence on ion carburizing of the steel. An apparatus in which works can transfer preheating, ion-carburizing and diffusion treating zones continuously was made for effective carburizing of steel. The gases were flown into above three zones with three different gas inlets. The hardness and microstructure of the works were investigated after ion carburizing and quenching. The steel is carburized deeper near the carburizing gas flow nozzle of the inlet than far from the nozzle. Hard surface layer fom1ed by quenching of ion-carburized steel.IntroductionGas carburizing is used for a surface hardening treatment which decreases fatigue and wear of the industrial parts used in automobile, machines etc. Ion and vacuum carburizing have been developed recently and applied to some industrial parts of restrictive purposes. The ion carburizing treatment which uses hollow cathode discharge (HCD ion-carburizing) is superior in energy saving, resource saving, environmental cleanness to the other carburizing treatment. Specially, carburizing energy can be saved in HCD ion-carburizing, because highly heated zone can be restricted in the range between work and subsidiary cathode where hollow cathode discharge arises, and the work is carburized in shorter tin1e in HCD ion carburizing method than other carburizing methods. Three treatments of preheating, carburizing methods and carbon potential controlling by hollow cathode discharge tried to be carried out in one continuous transferring series to carburize works more effectively, so the HCD ion-carburizing apparatus with continuous transferring system was made and gears of works were HCD ion-carburized in continuous transferring. The works were rotated themselves to get homogeneous carburizing by continuous transferring in glow of hollow cathode discharge."

Jan 1, 2000

By P. J. Harrington

The recovery and recycling of low concentration metal and other ions has traditionally been carried out using adsorption or ion exchange processes which, however, become uneconomical at higher concentrations, such as those that occur with many intermediate or waste streams where recycling is now being required. This paper describes the development of a process based on non-dispersive solvent extraction for the recovery of chromium (VI) from electroplating rinse water. During the chromium plating of steel, the concentration of chromium (VI) in the rinse bath rises to concentrations in the order of 100 mg/L when it becomes unusable and is then disposed of. The aim of this work was to investigate processes for recovery and recycling of the chromium in the rinse bath. The recovered chromium is required to be concentrated and purified before reuse. Tertiary amines have been shown capable of concentrating and purifying the chromium (VI) in solution. However, solvent extraction processes that have been applied to the recovery and reuse of metals from waste streams have had only limited success in the past, primarily because of the relatively high solvent losses when existing contacting equipment is used on low feed concentrations. Attempts to eliminate losses by immobilizing these complexing agents on substrates have not been successful. In order to control the losses and maintain specificity, a hollow fibre-contained liquid membrane has recently been trailed in a pilot plant to recover chromium from chromium plating waste streams. Details of the trial and modeling of the results are presented, and show that the level of losses is significantly reduced. However, issues relating to fouling still need to be addressed. This type of equipment has many applications in the recovery and recycling of a range of materials in the manufacturing processes.

Jan 1, 2003

By P. R. Seidl, R. C. C. Ribeiro, J. C. G. Correia

"More than 95% of asphalt pavement materials consist of aggregates. The highway and construction industries consume a huge amount of aggregates annually causing considerable energy and environmental losses. The aggregates are usually produced from neighborhood aggregate quarries or form natural aggregate sources. The use of marble and granite wastes from quarries as aggregates might help meet the increasing demands and slow down any detrimental effects on the environment. Chemical and physical results showed that the use of marble and granite wastes from quarries in the asphalt production is quite fusible. Consequently, granite sawmills would perform a clean technology. This technology would also have an economical impact by not spending on basalt extraction.IntroductionThe granite fines generated from sawmills of ornamental rocks comes as a great problem and it lacks undeletable solutions. This problem involves the preservation of the environmental and constitutes one of the subjects more critical the point of view of social beneficiation of the population. The Cachoeiro de Itapemirim County, Espírito Santo State, Brazil is an example, of this problem. In this area, the granite and marble fines generation is around 15.000 ton/year.The problems generated by these residues affect with more emphasis the animals, such as the cattle, which inhaled the water content fines of granite and this residue accumulate in their lungs. Other great problem observed is the sanded of the river and the reduction of aquatic life.This problem is beginning to be set out due to performance of Center of Mineral Technology (CETEM), and of several other organisms of Rio de Janeiro State, aiding the sawmills owner’s. This help consists of teaching the best procedure of discard the residues and studies for its use, for instance the production of mortars, tiles, bricks and road pavements [1]."

Jan 1, 2008