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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 Victor Bredykhin

The report is devoted to the investigation and improvement of processes taking place at contact of large quantities of water insoluble liquid and particles of solid phase in a pulp. Theoretical analysis and simulation of acting conditions have allowed to determine that after attaching of oleophilic particles on the «water-reagent» separation surface the break of a formed complex is taking place according to the reagent volume and for oleophobic minerals along the «solid-reagent» separation surface. As a result particles are selectively treated if the magnitude of the reagent adhesion to the surface of solid phase in water is great. The results of dispersion are influenced significantly by availability of sharp edges on the surface of real particles. They keep tree phase perimeter of moistening. It is possible to fix reagent in the form of lens whose contact angle is significantly smaller in comparison to the thermodynamic angle. In adhesion dispersion the reduction of reagent volume, covering the equal area of particles surface is possible when the reagent is in a pulp in the form of thin films on the «water-gas» separation border. The process is tested in laboratory conditions as well as at pilot concentrating mills in flotation of sulfide ores, non-ferrous metals (copper-molybdenum ore), native sulfur and coal.

Jan 1, 2006

Iron(II), sulphur dioxide and sugars such as lactose are potential reducing agents for manganese dioxide to produce manganese(II) for subsequent hydrometallurgical treatment. The leaching of limonitic laterite and manganiferrous ores with sulphur dioxide produces iron(II) which in turn can catalyse the leaching of manganese dioxide in acid media. This paper presents a critical analysis of the kinetics of reductive dissolution of synthetic manganese dioxide and manganese ore to compare and contrast the effect of sulphur dioxide and iron(II) in acid media containing sulphate or perchlorate anions. Both one-electron and two-electron mechanisms are considered in the case of sulphur dioxide. The current knowledge on chemical speciation is used to construct an Eh-pH diagram to show the effect of complexation of Mn(II), Fe(II) and Fe(III) with sulphate. Heterogeneous and electrochemical reaction kinetic models are combined to propose reaction mechanisms which rationalize the dissolution kinetics.

Jan 1, 2003

By Naoki Hiroyoshi

It is generally accepted that ferric ions are effective for leaching chalcopyrite as an oxidant and ferrous ions contribute to the leaching only as a source of the oxidant ferric ions. However, this paper shows that ferrous ions are more useful for leaching chalcopyrite than oxidant ferric ions in sulfuric acid solutions in air at ambient temperatures. Leaching experiments and dissolved oxygen consumption measurements were carried out with a very pure chalcopyrite and 0.001 - 1 mol dm-3 sulfuric acid solutions containing 0 - 0.1 mol dm-3 ferric or ferrous ions at 303 K. Chalcopyrite oxidation with dissolved oxygen was promoted by ferrous ions but suppressed by ferric ions. As a result, the amount of extracted copper was larger with ferrous ions than with ferric ions. Effects of Thiobacillus ferrooxidans on the ferrous promoted chalcopyrite leaching were also investigated and discussed based on the experimental data.

Jan 1, 1999

By Jason Graetz

Aluminum hydride is a covalent, binary hydride that has been known for more than 60 years and is an attractive medium for on-board automotive hydrogen storage, since it contains 10.1 % by wt. hydrogen with a density of 1.48 g/ml. There are at least 7 non-solvated AlH3 phases, namely a, a', a, ?, d, e and ?. The properties of a-AlH3, obtained from the Dow Chemical Co. in 1980, have been previously reported. Here we present a description of the thermodynamic and kinetic properties of freshly prepared a, 0 and y phases of AlH3. In all cases the decomposition kinetics are appreciable below 100" C and all will meet the DOE 2010 gravimetric and volumetric vehicular system targets (6 wt% H2 and 0.045 kg/L). However, further research will be required to develop an efficient and economical process to regenerate AlH3 from the spent A1 powder.

Jan 1, 2006

By P. Stantke

In recent years the CollaMat process has been used successfully worldwide in a number of copper electrorefining tankhouses as an instrument for measuring the glue concentration and optimizing cathode quality. Owing to its measuring principles the CollaMat can be used not just for measuring the concentration of active glue but also the activity of other substances, which have an impact similar to glue on the copper deposition. In SX-EW plants guar is frequently used instead of glue as a levelling additive. In our laboratory the effect (activity) and the decomposition rate of guar in copper electrolyte was examined. As expected, the results show that guar has an effect similar to glue on the copper deposition. However, at the same temperature, a greater quantity of guar is required to achieve the same results. As with glue, the decomposition rate (due to hydrolysis) of guar is strongly dependent on the temperature. Therefore, in practice, its on-line monitoring is necessary to guarantee the same guar activity at any time.

Jan 1, 1999

By Ronald J. Roman

The shrinking core model for coarse particle leaching has been generally accepted as describing the leaching of a copper oxide or sulfide ore. However, when a mixed oxide/sulfide ore-is leached this model can not be used in its simple form because at least two and possibly three separate leaching processes are occurring simultaneously (dissolution of oxide copper minerals, secondary copper minerals and primarily copper minerals). It has been impossible to isolate their individual leaching curves from the recovery/time curve generated by the column leach test. This paper describes a tests program carried out at the Groupo Mexico, Mexicana de Cobre's La Caridad operation in which the individual recovery/time curves for the leaching of copper oxide mineral, secondary copper mineral and primary copper minerals were developed from standard column leach tests. Once the individual recovery/time curves were developed scale-up of the column leach test results to the commercial heap leaching operation is possible by using the shrinking core model.

Jan 1, 1999

By L. B. Tsymbulov

At present data on thermodynamic properties of metallic melts, containing copper and ?iron family? metals, is rather limited. Determination of the activity of metallic melts components under high temperature by experimental methods requires high level of labour inputs. With this it is not always possible to obtain the results with high level of accuracy. Due to that in a number of cases it is more appropriate to apply different methods of analysis, with the help of which there can be calculated thermodynamic properties of ternary and even more complicated systems, prominent thermodynamic properties of binary systems being used as a basis for these calculations. This work presents the results of calculations of different components activity and activity ratio in such ternary system melts as Ni-Cu-Fe, Ni-Cu-Co, Fe-Cu-Co and Fe-Co-Ni. Good compliance of calculations results with those obtained in the course of reliable experimental investigations fulfilment is demonstrated. There are presented the results of activity and activity ration analysis for some compositions of Cu-Ni-Co-Fe system.

Jan 1, 2006

By Kimio Itagaki

As a fundamental study for smelting the copper matte with high contents of arsenic and antimony in a strongly reducing condition, phase relations between the liquid matte and copper-rich alloy phases in the Cu-Fe-S-As or -Sb quaternary system and between the liquid matte and iron-rich alloy phases in the Cu-Fe-S-As or -Sb system saturated with carbon were determined at 1473 K by a quenching method. Activities of arsenic and antimony in these systems were also measured at 1473K by Knudsen cell-mass spectrometry. Furthermore, distribution ratios of silver, gold and platinum between the liquid matte and copper-rich or iron-rich alloy phases were determined in relation to the arsenic or antimony content in the systems. On the basis of these data, the elimination of arsenic and antimony from the matte to the iron-rich alloy (speiss) and the recovery of precious metals in reduction smelting of the copper matte were evaluated. It was suggested that the addition of pig iron to make a strongly reducing condition and form the iron-rich alloy, which is fluid at smelting temperatures, will be useful for fixing arsenic in the speiss.

Jan 1, 2006

By Maria de Campos

The pre-reduction behaviour of chromite particles in methane-argon and methane-hydrogen gas mixtures was investigated between 1050°C and 1250°C. Loose bed of chromite particles were reacted in a vertical tube furnace under a pre-set gas mixture predetermined time intervals. Metallization results were obtained for the Cr and Fe components by chemically analyzing the reaction products. SEM-EDAX techniques and X-ray diffraction were employed to elucidate the reduction mechanism. It was found that higher reduction kinetics and higher Cr:Fe ratios in the metal phase would be achieved when hydrocarbon gas was used in comparison to classical carbothermic reduction at a given temperature. The reduction rate was generally bulk gas mass transfer controlled to the reaction site for initial stages which then was followed by ionic diffusion rate control. It is proposed that methane did not partake directly in the reduction but cracked, presenting the reaction site with hydrogen gas and atomic carbon, which was able to immediately react at the immediate area of reduction regeneration CO and H2 and thus maintaining a low partial pressure of oxygen at the reaction site.

Jan 1, 2006

By S. F. Cheng

Among the many extraordinary features of the rare earths are their magnetic and magnetoelastic properties. The rare earths, e.g. Tb, Dy, Nd, Sm, are known worldwide for their large magnetocrystalline anisotropy and magnetization, which has led to the importance of magnetic rare earths as vital ingredients of modem permanent magnets. In this paper, we focus on the strain dependence of these giant effects which gives rise to huge magnetostrictions, magnetomechanical couplings, and ?E effects. Magnetostrictions greater than 10-3 have been measured at temperatures as high as 500 K. At low temperatures magnetostrictions reaches -1%. ?E effects - 10. No other solid state material has matched these values. A proper balance of magnetic anisotropy and magnetostriction, plus a proper choice of crystal axes lead to alloys which can switch large quantities of energy between the internal (magnetic) and external (mechanical) states with the application of small triggering magnetic fields. In addition to the traditional use of these materials in transduction, they are particularly valuable for smart systems where reliability and robustness are needed such as active structure stiffening and active vibration control.

Jan 1, 1997

By Jeffrey F. Adams

Gypsum fouling is a common problem in the hydrometallurgical industry. It is a particular problem in free sulphuric acid neutralization, or iron removal operations where sulphates are removed from aqueous solutions by the addition of calcium-containing bases. Previous work revealed a strong correlation between the degree of gypsum supersaturation in the reactor and the rate of scale growth indicating that scale formation and growth are primarily controlled by chemical phenomena. However, the chemical behaviour of gypsum is variable and unpredictable with solution chemistry and temperature. Many of the "rules of thumb" that are used to predict its behaviour (and avoid fouling) are in fact based on gypsum solubility in water, rather than on real mixed metal sulphate systems. However, despite this unconventional solubility behaviour, we have been able to accurately model it in Ni, Mg, and Zn containing solutions over a wide range of temperature (25°C-90°C) and solution concentration (0-6 m) using the OLI simulation software. Furthermore, by studying fouling rates in a simulated continuous neutralization reactor, the relationship between process conditions and fouling rates were explained for the first time. This has led to an understanding of how techniques for minimizing gypsum fouling work.

Jan 1, 2003

By Helena Byrdziak

KGHM Polska Miedz S.A. is a significant European copper producer with production of 447,000 mtpy, operating three underground mines and three smelters. The company has been involved for years in environmental activity, which was stimulated not only by the company itself, but by the development of environmental regulations as well. The first set of regulations, concerning water protection, was' established in Poland' in 1974, while a comprehensive environmental law was passed in 1980. This law in general requires industry to submit all data of environmental significance to the local authorities. Based on this data, they establish limits concerning emissions into the air, water and ground, the amount of wastes produced and the means of their disposal. A company has to pay fees for each tonne of emitted substances and stored wastes. When the emission of a substance exceeds the limit, the company has to pay a penalty which is about ten times higher than the fees. This approach in general is effective because it forces companies toward: reduction of their emissions. The problem is that the law is constantly subject to change and is becoming not only more restrictive but is involving more and more bureaucracy.

Jan 1, 1999

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 Mingzhou Li, Lin Wu, Changren Tong, Fengli Yang, Shaohua Yang

"According to characteristics of Tm, Yb and Lu enriched oxides composition and problems in its traditional extraction separation process, the computer simulation of a optimized fuzzy extraction separation process, in which three products with high purity(>99.99%) could be obtained at same time, was carried out. Distributing Curves of every element in both organic and aqueous phases were worked out. Distribution rules of rare earth elements in every stage of the optimized extraction process were studied. The computation results of economical and technical index showed the consumption of the acid and base chemical reagents in the optimized process would be saved more than 30%.IntroductionFor the solvent extraction separation process of rare earths, countercurrent extraction process was widespread in the industrial practice. Normally, rare earth ions were extracted by the saponificated extractant and transferred into the organic phase, where the acidic extractant was saponificated by the base firstly. Then, the loaded rare earth ions were stripped from the organic phase into the aqueous phase by the acid. Therefore, the acid and the base were the main consumptions in the process, and the equilibrium acid of the stripped rare earth solution was one of the main pollution resources. Meanwhile, for the heavy rare earths, such as Tm, Yb and Lu, stripping was more difficult, and the equilibrium acidity of the stripped rare earth solution was higher, so the acid consumption increased greatly."

Jan 1, 2012

By J. M. Casas

This work presents the development of an ionic equilibrium model and its use to simulate the distribution and concentration of chemical species (speciation) in sulfuric acid - cupric sulfate solutions in the 0-2 pH range, 0.1-10 gpl copper concentration range and 15-45°C temperature range. The model consists of a set of equations which represent the equilibrium relationships for the ionic reactions and the mass balances for the components present in the system. The effect of ionic strength was taken into account by correcting the equilibrium constant in concentrated solutions. Several species can be formed at different pH and temperature values, the principal being: HSO-4, SO42-, CuSO4(aq), Cu2+, and H+ in order of increasing solution acidity. Simulations show that concentrations are highly dependent on pH. The sulfuric acid speciates mainly as bisulfate ion (HS0-4) and hydrogen ion (H+) at pH values lower than 1. The model presented in this work can be applied to predict and analyze the solution composition in electrolytic copper processes such as electrowinning, electrorefining and electrodialysis, as well as the purification of various industrial solutions.

Jan 1, 1999

By Neil E. Izatt, Ronald L. Bruening, Steven R. Izatt

"IBC has developed environmentally friendly Molecular Recognition Technology (MRT) processes to selectively extract, recover, and purify a wide range of metals from a variety of process streams. The incorporation of MRT into process flow sheets can improve the economics of the processes. MRT separations are effective even at low (mg/L to \i%JV) metal levels. MRT processes are sustainable, being economically viable, energy efficient, and environmentally friendly as well as having a low carbon footprint. Examples of MRT processes will be presented and discussed involving platinum group metals, gold, rhenium, and other metals of interest to the mining community.IntroductionA significant portion of the earth's precious metal resources has been moved during the past century from underground to above ground [1]. This movement has important economic, health, environmental, ecological, and sustainability implications for the earth and its population. There is concern that recycling of certain precious and specialty metals from end-of-life (EOL) electronic wastes (e-wastes), catalyst wastes, mining waste streams, and other waste products such as rechargeable batteries is not adequate to maintain supplies of these metals sufficient for future needs [2-4]. Improved metal recycling rates and more efficient metal recovery from the enumerated wastes would significantly reduce the amount of virgin metals that must be mined to support our lifestyle [5]. More efficient separation procedures in ore processing flow sheets and more effective recovery of metals from low-grade waste streams would reduce metal loss in the mining industry."

Jan 1, 2012

"Silver is traditionally recovered in base metal smelters (lead and copper), or as a by-product of other precious metals (gold and/or PGM's). This paper presents the results of non-conventional techniques to recover silver from complex materials. The PLATSOL® process has been developed to recover, in one step and without the use of cyanide, base metals (copper, cobalt, nickel) and precious metals (gold, PGM's) from sulphide concentrates too low in grade to enter the mainstream extraction processes. Silver is only partially recovered in solution with gold and the PGM's during the PLATSOL® process. However, the silver minerals are transformed into silver chloride, which can then be recovered from the PLATSOL® residue using conventional techniques. Some South American silver concentrates contain levels of impurity (mostly arsenic) so elevated that the penalties incurred significantly affect the process economics. The present results have shown that a low temperature calcination process transforms the concentrate into a product well suited for traditional recovery treatments. Metallurgical details will be provided, as well as the results of mineralogical studies that helped clarify the process mechanisms.IntroductionSilver occurrences in nature are very diversified, and, therefore, primary silver is produced as a by-product of many base metal and precious metal operations [1], as well as a co-product of most gold ores. However, difficulties can arise when high temperature processes are used for refractory gold ores or copper concentrates, or when the silver concentrate contains impurity elements such as arsenic that trigger high penalties."

Jan 1, 2012

By Jeong-Hwan Kim

The liquid-liquid reactive process (solution process) is often adopted as a synthetic method for precipitated calcium carbonate (PCC) in laboratory studies for its simplicity in operation or ease in controlling process variables. Still, PCC are produced commercially by passing carbon dioxide through a milk of lime, i.e., by a gas-liquid reacting method (carbonation process). Few studies on the carbonation process have been conducted, since the process variables are interrelated and difficult to control compared to the solution process. In this study, both carbonation and solution processes were employed to study the polymorphs of calcium carbonate and growth rate of PCC crystals. The effects of the characteristics of limestone ores as a raw material in the synthetic system of PCC on the synthetic characteristics of PCC were also investigated. To control the nucleation rate in the synthetic systems, the shape factor was considered most important. Single-phase aragonite PCC could be synthesized under a variety of controlled experimental conditions such as ionic strength, solution composition, concentrations of additive ions, and temperature.

Jan 1, 2006

By Yves Fautrelle, Kader Zaidat, Hervé Combeau, Miha Zaloznik, Mohammed M'Hamdi, Bachir Saadi, Xiaodong Wang, Knut Omdal Tveito

"Numerical simulations of macrosegregation formation during horizontal solidification of a hypoeutectic Sn-Pb alloy in a rectangular cavity is presented and compared to experimental results. The experiment involves a melting phase, a holding stage at constant temperature with/without application of electromagnetic stirring, and finally solidification. We simulate all stages of the experiment and study the segregation of Pb throughout the experiment. A twophase volume averaged model is used for the numerical simulations, accounting for thermosolutal convection and assuming perfect microscopic mixing (lever rule). The influence of the melting phase and the electromagnetic stirring is studied with different cases to illustrate the consequences on the flow pattern and Pb segregation. The numerical simulations are compared to the experimental data and the impact of chemical inhomogeneities prior to solidification on macrosegregation formation is discussed.IntroductionMany extensive investigations have been performed so far on the solidification of metallic alloys. However, the melting process of metallic alloy has not attracted attention in a same manner. Nevertheless, melting of alloy may put forth peculiar effects as described in the present paper. It has been observed from a benchmark experiment [1, 2] that significant stratification might arise during the melting process of Sn-Pb alloy. That effect was put forth thanks to the analysis of the experimental temperature distribution which indicated that the convective fluid flow was almost zero. The effect was enhanced when the lead composition was higher (above 6wt.%). The present paper is aimed at confirming that the melting of an alloy containing a heavier solute may be accompanied with a stratification of the solute which exerts a stabilizing effect on the convective fluid flow. Results obtained from numerical modeling are compared with experimental data obtained from the benchmark facility."

Jan 1, 2012