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By David Deglon, Martin Harris, Mehdi Safari

This paper investigates the effect of energy input on the flotation of galena in a novel oscillating grid flotation cell (OGC). Oscillating grids generate near ideal hydrodynamic environments, characterised by turbulence which is relatively homogeneous and isotropic. Previous work was limited to quartz (-100 µm). Galena (-150 µm) was floated in the OGC at power intensities from 0.5 to 3 W/kg using 0.13, 0.58 and 0.82 mm mean bubble sizes (d10) and at three collector dosages. Results show that the effect of power intensity on flotation kinetics is strongly dependent on both particle and bubble size. For fine particles (-19 µm), increasing energy input increases the flotation rate at a low collector dosage but leads to an optimum at both the moderate and high collector dosages. For intermediate particles (+19-38 µm), increasing energy input has no effect on the flotation rate at the low collector dosage but leads to an optimum at both moderate and high collector dosages. For coarse particles (+38-150 µm), increasing energy input has no effect on the flotation rate at the low collector dosage and leads to a general decrease at both moderate and high collector dosages. Optimum conditions for fine particles are using small bubbles at a moderate collector dosage and an energy input of around 2 W/kg. Optimum conditions for moderate particles are using small bubbles at a high collector dosage and energy inputs of around 1.0 W/kg. Coarse particles do not benefit from agitation.

Jan 1, 2014

By G. S. Hansford, G. E. Searby

The rate of bioleaching of pyrite at 70ºC by a thermophilic archaeal culture was measured as a function of the solution redox potential by the staged addition of pyrite to a batch system. The results were compared to the rate of ferrous iron oxidation over the same potential range to determine the applicability of the multi-sub-process leaching mechanism developed for mesophilic bioleach systems.

Jan 1, 2003

By Markus A. Reuter, Albert Scholte, Ewoud V. Verhoef, Gerard P. J. Dijkema

"A dynamic, interactive map has been developed of the life cycle of a number of metals, from mining through to minerals processing, metal production, product manufacturing, recovery and waste management. Whilst the existing metal process network and waste management infrastructure provide substantial scope for (product) design, these also limit change because of the strong path dependency of industry and infrastructure development. The metal production network is complex, as it consists of an interconnected and integrated system that incorporates multiple production routes for a spectrum of metals. More often than not, the production or recovery of a single metal is related to or dependent on the generation or recovery of another. The effects of these other metals is of great importance. In order to realize the potential economic importance of impurities, research and development have integrated the processes of copper production with those of lead and zinc, and connected the processes to those of among others silver, bismuth, tin and platinum group metals (PGMs), for example. The recovery of these elements from the interconnected circuits is extremely complex, as most of the elements must be circulated between two or more circuits before they are concentrated enough to make their extraction possible, and their recovery as a compound profitable.From such a system’s perspective, it can easily be seen that a complication for solid waste management has arisen through the development of products (consumer goods) that bring together metals that are not linked in natural resources. As a consequence, many of these materials are not compatible with any process in the metals production network that was developed for the processing of primary, natural resources, optimized for the processing not only of the primary metal but also for all mineralogically associated minor valuable and harmful elements. The formation of large or complex residue streams or undesired harmful emissions then inhibits processing and recovery of said products at their end-of-life. Another complication is that any change to the system (in metal production, SWM or product design) affects the system configuration. Due to the changing demands for metals as a result from the changing products made from the metals for example, the relationships between the processes in the interconnected metal production systems change. This affects both the demand for old scrap (required amount and grade) from waste management, and the environmental profile of the metals. Preferably, therefore, product designers, waste processors and metal producers must cooperate to realize optimal metal recovery in processing discarded consumer products."

Jan 1, 2003

By A. Gueciouer, A. Akkouche, K. Chalah, A. Benmounah

"Drilling solid waste is a typical industrial solid waste, and it is a major pollutant source to ecological environment. Generally, waste management dewatering systems separate solids and fine particles from the liquid phase of drilling fluid, thereby leaving a clarified aqueous solution and allow the cleaning of waste fluids. Typically, dewatering waste management systems clean drilling fluid through coagulation, flocculation and/or mechanical separation. Chemicals used in dewatering are based on the coagulation-flocculation process, which it facilitate the removal of suspended solids and colloidal particles. The factors which can promote the coagulation-flocculation are velocity gradient, contact time, and PH. The objective of this work is to optimize a formulation adequate for dewatering based on the coagulation-flocculation process used coagulant (Aluminum sulphate), anionic flocculants (Partially Hydrolyzed Polyacrylamide) and anionic polyelectrolytes (in solid form with linear chain with very high molecular weight). The results obtained show the good efficiency of the coagulant and flocculants. INTRODUCTION Rig site dewatering of drilling fluids with recycling of processed water can help an operator to comply with environmental rules by reducing volumes of waste and reducing long term liabilities. It can also reduce disposal costs and provide a cleaner drill site overall. Most of the environmental concerns during the 1980s involved hazardous materials and toxic wastes. Drilling fluids, many of which are chemically benign, have escaped many of the difficult-to-comply-with rules and regulations. During the 1990s, however, operators may be required to submit a written plan for liquid waste reduction for even nonhazardous materials. Many states and local agencies may institute total bans on oil field wastes. Drilling rigs typically produce about 1 bbl of liquid waste for every 1 ft of hole drilled. Thus, a typical drilling operation can produce a large quantity of waste [1]. To improve the dewaterability of sludge, different pretreatment processes have been widely studied and developed including thermal, chemical, magnetic, mechanical, acoustic, electric, electro-acoustic and their hybrid treatment processes [2]. Rig site dewatering (figure 1) is the process of injecting coagulants or flocculating chemicals into the mud entering a large clarifying centrifuge. Coagulation occurs when the solid and allowing it to be attracted to other solids by van der waals forces. Flocculation is the binding of individual solid particles into aggregates of multiple particles. It is physical, rather than electrical, and occurs when one segment of a flocculating polymer chain absorbs simultaneously onto more than one particle [3]."

Jan 1, 2018

By Sonia Helle, Ursula E. D. Kelm

"From a metallurgical point of view, acid leaching of oxide zone copper ore is considered in the first place in terms of ore grade, whole rock mineralogy, rock granulometry, crushed aggregate size distribution, porosity, permeability and corresponding fluid flow characteristics. Despite exhaustive physicochemical and general mineralogical characterization, drops in copper recovery occur and are often attributed to and “unquantified mineralogical misbehaviour” of the gangue phases. This study establishes an experimental link to monitor and quantify the chemical interaction of chrysocolla, malachite and atacamite with reactive gangue phases.Laboratory-scale sulphuric acid (15%) leaching in small columns is carried out using a synthetic rock composed of 57% quartz, 1% ore phase, and 42% reactive gangue. Gangue phases were selected to represent mineralogy found in argillic, advanced argillic, and propylitic alteration zones. Exotic copper ores of Codelco Norte (in particular Mina Sur) served as model for the modal distribution of mineral phases. Natural reactive gangue phases (<200 Tyler mesh) were chosen as pure as possible: Saz-1 and Swy-1 montmorillonites, KGa-1B and KGa-2 kaolinites (all Clay Mineral Society, USA, Source Clays) Nau-2 nontronite, Imt-1 illite (both Clay Mineral Society Special Clays) and Chilean mordenite, laumontite and bentonite. Ore phases are: mineraloid chrysocolla from Radomiro Tomic (Codelco Norte), reagent grade malachite and a purpose synthesized atacamite-paratacamite mixture. Complete chemical, physicochemical and mineralogical characterizations were carried out for ore and gangue phases.The following observations hold for samples with and without mineralization: Smectite-rich gangue increased up to 75% in volume. Once wet, air-filled vesicles formed due to the rapid sealing effect of overlying smectite in the column. No volume change occurred for illite, mordenite and kaolinite gangues. For kaolinite mixtures acid puddles formed on top of the column during initial leaching due to the delamination and barrier formation of this phyllosilicate. Fluid recovery was <60% for expandable phases and reached up to 80% for non-expandable mixtures. These observations confirm the very low extractions obtained in ore with a combined smectite – kaolinite gangue for Mina Sur. The most important mineralogical changes observed in the solid residues are: reduction of basal smectite phase reflections (XRD), and slight loss of illite intensities. This is also reflected in the major element composition of the residues, which demonstrate a loss of Mg, Mn, Ca, Na, K followed by Fe, Al and Si; with their proportions depending on the starting materials. Furthermore, alunogen and meta-alunogen formed, with related phases coquimbite (illite) and godichite (nontronite) also depending on gangue mineral chemistry. For laumontite samples, meta-alunogen and alunogen precipitated from the leachate."

Jan 1, 2003

By V. Avzian Belozersky reg 453524, Vasily V. Lodeischikov, Adolf F. Panchenko, Til E. Vidusov, Olga D. Khmelnitskaya, Vladimir E. Dementyev

"Presently, there is a number of gold deposits which cannot be developed using the conventional technologies with acceptable economic indices due to low gold content, high depth of ore occurence and other conditions. For such ores, an innovation technology of underground gold leaching in the place of their occurrence is of special interest. The technology excludes ore mining and hoisting to the surface. This enables the production cost of 1 g of gold to be considerably reduced in comparison with conventional methods of gold recovery.The Maminskoye deposit oxidized ores were chosen as the subject of underground leaching because they are ideally suited for this purpose due to their composition and hydrological parameters. The ore reserves within the underground leaching block are 90, 000 t with 0.7 g/t average gold grade.An experimental system for underground leaching with a throughput of 15 cubic m solutions per hour was developed. A combined filtration-and-infiltration system of the ore massif development by holedrillingwhere pregnant solutions are air-lifted was worked out.The underground leaching flowsheet includes Au dissolution by chlorine-containing solutions, Au adsorption from solution onto active carbon, carbon concentrate ashing and calcine melting to produce Dore metal."

Jan 1, 2003

By Rodolfo Silva, Antonio Peres, Afonso Martins, Gilberto Ramalho, Mario Cabello

The consumption of aggregates in civil construction has increased considerably in Brazil for the last years. The extraction of sand and gravel generates significant environmental impacts. As the quarries and sand deposits are getting exhausted near the big cities, the price of aggregates is increasing. Meanwhile, the extraction of quartzite (dimensional stone) in the state of Minas Gerais has been done mostly in small quarries, with very low recovery, generating approximately six million tons of wastes a year, which causes pollution, increases final prices of products, decreases the life time of quarries and ends up in the closure of enterprises. The government agencies and the quarries’ owners understand that only by finding applications to wastes there will be development to the sector. The aim of this investigation was to study the application to the quartzite wastes as aggregate in the civil construction. Samples of quartzite wastes collected in a quarry were characterized by petrographic analyses. Laboratory tests of crushing and grinding were done to analyze the viability of reducing the size of coarse material to a finer one to be used as raw material in industrialized mortars and concrete pre-molded components.

Jan 1, 2014

By Stefan Mutz, Thomas Pretz, Jörg Julius, Frank Hilbk-Kortenbruck, Aachen, Hartmut Harbeck

"The annual global production of primary aluminium was about 22 million tons in the year 2000. This represents the second largest production rate in the world market after steel. Experts are predicting that the global demand for aluminium will rise in the near future.In contrast to other metals such as copper, the recycling of aluminium is considered relatively difficult. There are two main alloying groups, namely cast and wrought. In the case of aluminium it is important that the constituents within the scrap aluminium to be smelted are clearly identified. Within the secondary remelting process alloying does take place, but a removal of unwanted metal constituents is problematic. Therefore mixed aluminium scrap (not genuine in-house collected material) can only be used to produce cast aluminium. Thus, in other words a down-cycling of wrought (extrusions and rolled) products occurs. However, in spite of these difficulties there is an increasing trend to produce aluminium from secondary scrap (approx. 35% in Germany). Similar trends have been identified in the USA and other industrialised countries. This development is mainly caused by the high energy consumption for the production of aluminium from bauxite. Producing aluminium from scrap is saving about 95 % of the energy in comparison to the processing of primary raw materials.An improvement in sorting technology is necessary to separate wrought and cast alloys of aluminium as the absolute amount of recovery from old scrap is higher than the demand for cast.This contribution presents some alternative methods, utilizing automatic picking technologies, which will be used to separate secondary aluminium in the future. During the recent years, some major progresses have been made in automatic picking technologies for different applications in the processing of primary and secondary materials.For the sorting of aluminium scrap a special additional sensor will be necessary. The best detection will ultimately be based on online elemental analysis of single particles. First investigations in the field of laser based systems for these applications have already been performed several years ago. One of the laser based techniques is the laserinduced breakdown spectrometry (LIBS)."

Jan 1, 2003

By Vincent C. Smith, Agit Singh, Daniel de V. van der Spuy, Bernard Muller

"Process control in the minerals industry is made difficult by factors such as the multivariable nature of the processes, noise, many disturbances, the changing nature of the processes, nonlinearities, process constraints, slow responses and large deadtimes. A good example of such a process is a milling circuit, where all these problems are experienced. Since model predictive control (MPC) effectively handles most of these difficulties, Mintek decided to develop, customise and test an MPC controller for milling control.Conventional MPC uses a dynamic model of the plant to calculate the future (predicted) plant outputs based on the movements of the manipulated variables in the past. The future moves of the manipulated variables can then be calculated using an optimisation algorithm that will minimise the difference between the setpoints and the predicted outputs. The least squares optimisation method is the quickest, but it does not cater for process constraints. Constraints can, however, be handled explicitly by using a quadratic programming optimisation method. This method ensures that the variables stay within the constraints at all times, but the calculation procedure is much more computationally intensive.• modifying MPC for the Minerals Processing IndustryIt was found that in order to obtain good, robust control using MPC in the minerals processing industry, the conventional MPC algorithm had to be adapted. The MPC controller was first tested on an extensive milling simulator, which was specifically developed for that purpose. Problem areas were identified and the MPC controller was specially adapted to accommodate for these difficulties. Some of the adaptations to the conventional MPC algorithm and special features added were as follows:Since milling plants contain many integrating processes (e.g. sumps), and integrating errors can cause offsets and poor control, it was essential that integrators be handled explicitly. This problem was solved by adapting the algorithm and also using an integrating error portion to compensate for integrating errors.Constraints on the inputs and outputs adversely affected the control. The controller using simple least squares optimisation was tuned with the constraints in place, while the maximum expected setpoint changes were made. This ensured that the process would be able to handle most setpoint changes up to these expected values without violating the constraints. A later improvement on this method was the incorporation of a quadratic programming algorithm to perform the optimisation. This method handles limits explicitly and was shown to perform better than the least squares methods (at the expense of a much higher computational cost)"

Jan 1, 2003

By P. M. Solozhenkin

"Galvanochemical process (GChP)) cleaning of sewages is realized in the field of shortcirquited galvanic elements from the mixture current the materials place in purification’s solution and form multitude galvanopairs without external electric field in presence oxygen of the air. The galvanochemical process is electrochemical process utilizing galvanic pairs: coke - iron, iron - copper and others and process does not require chemical reagents.The effect of basic parameters of the cleaning effectiveness have been studied depending on oxidizing of galvanopairs. Adjusting nature, type of galvanic pairs and forming three component system possible to enlarge emf circuits to 2.378 V.The role of ?2, as basic agent, for generation of hydrogen peroxide and hydroxyl ions.It was stated, that removing of metal ions from solutions occur mainly on account of sorption and hydrolytic sedimentation of iron oxihydrates.Determined separate stages of the process: coagulation, sorptions of admixtures on freshly formed ferric oxides and oxidizing destruction of organic components of effluents in presence of ?2 ? ?2?2. Shown efficiency of the method for removing of Cu, Cr, Ni, Zn, As ions, as well as fluoride, phosphate and cyanide anions and oil products, surface-active and flotation reagents. Cleaned water can be recycled for some processes non-critical toward residual concentration of admixtures, as total salt contents is lowered on 60-75 % and reaching limits of concentration for toxic components.The concept of high power unit creation was developed, and galvanochemical pulsator is presented. The pulsator is not expensive, and exploitation expences are low, as well as servise is simple with high effectiveness, and capacity. The galvanoflotation process is developing, combining galvanochemistry and flotation of hydrofobic admixtures (oil, surface-active agents).The galvanochemical flotators are presented."

Jan 1, 2003

By Stephen J. Harker, John Knights, Randolph A. Pax, Glen A. Stewart

"Mineral samples were obtained from different stages of a mineral processing circuit used to extract the copper and gold rich mineralogical phases. The aim of this work is to characterise the quality of the samples at different stages of processing. The samples were taken of the head grade, tailings, cyclone overflow and the final concentrate.Characterisation of the samples was determined using Cu-Ka X-ray powder diffraction and Fe57 Mossbauer spectroscopy. These measurements will be presented and discussed in terms of the enrichment of the ore, showing the removal of magnetite and quartz through the processing, the final concentrate being rich in chalcopyrite and pyrite. This data also shows the utility of Mossbauer spectroscopy to provide mineralogical phase information directly.Mossbauer spectroscopy is a tool to determine the material phases of a sample. It is a nuclear based technique which measures the amount of attenuation of a narrow Doppler shifted source energy as it passes through a sample. The attenuation depends on the amount of resonantly absorbing material in the nuclear radiation path from the source to the detector. Synchronous detection of the doppler shifting velocity and the nuclear radiation count gives a Mossbauer spectrum. By convention, the energy axis of the Mossbauer spectrum is displayed in units of velocity.Figure 1 shows Mossbauer spectra obtained for a sequence of samples throughout a processing plant. These spectra show the removal of magnetite and the concentration of chalcopyrite and pyrite. Optical microscopy results indicated a significant component of bornite not witnessed with Mossbauer spectroscopy. Closer examination showed that optical microscopy assays over estimate the bornite component."

Jan 1, 2003

By Naoki Hiroyoshi, Hajime Miki, Tsuyoshi Hirajima, Masami Tsunekawa

"Acidic solutions for chalcopyrite leaching contain cupric, ferrous and ferric ions, and the oxidizing power of the solutions is indicated by a redox potential, determined by the concentration ratio of ferric to ferrous ions. This paper reviews our previous studies on the redox potential dependence of chalcopyrite leaching in sulfuric acid solutions. Leaching experiments indicated that copper extraction rate was accelerated by cupric and ferrous ions , and was higher at potentials below a critical value (critical potential) in the presence of these ions. This was in good agreement with the results of electrochemical measurements, i.e. in the anodic polarization curves for a chalcopyrite electrode, active-passive behavior was observed when cupric and ferrous ions co-exist, but the activation at low potential did not occur without these ions (Figure 1). The analysis of the AC impedance spectra for chalcopyrite electrode indicated that a high-resistance passive layer grows on the chalcopyrite surface without cupric and/or ferrous ions, and that coexistence of these ions causes a formation of another product layer and inhibits the passive layer growth at low potentials.These results are explained by a reaction model assuming the formation of intermediate Cu2S due to chalcopyrite reduction and the subsequent oxidation of the Cu2S. The critical potential corresponds to the redox potential of the Cu2S formation and the predicted values matched with the experimental results. Catalytic effect of silver ions on chalcopyrite leaching was also discussed based on experimental results and the above model."

Jan 1, 2003

By Vladimir Grujic, Milorad Grujic, Ivan Djurkovic, William Riggs

"In this paper, we have studied efficiency of different chemical structures of frothers on copper ore Majdanpek. The goal was to find out the best suitable chemical structure, which allows good bubble formation, size and interaction, forces on mineral surface. The particle size distribution was between 10 and 100 µm. Our research was oriented on three groups of frothers: alcohols, poly glycol ethers and poly glycols.We also used different collectors based on similar or less similar alcohol group in chemical structure as in frothers, expecting higher stability of air bubble in contact with copper minerals. Minimal potential energy was determinate in the hydrodynamic conditions for different particle sizes. It was founded that it is proportional to air bubble volume on 0.88° and contra proportional to the kinematics viscosity of pulp.Analyzing the results, we find out that poly glycols decreased surface tension the most. Also, it increased amount of coarser particles to the top of pulp. This group is less sensitive to pH value compared to the others too.From the class of frothers with higher efficiency in flotation process, we pointed OrePrep X-75 and X-133 as frothers with expressive frothing characteristic in the alkaline and low alkaline circuits. Special suitability of those frothers for floating copper minerals makes their hetero polar molecules with more than one hydrocarbon radicals connected to one polar group. However, those froters have no nether high or low solubility and are non-ionization. Those froters indicate some small collecting characteristics too. In dispersion systems, those two frothers make two types of bubbles: smaller di < 1.2 mm; V = 0.0008 cm3 and middle di < 16 mm; V = 2.2 cm3 (di – Bubble diameter, V – Bubble volume). Transportation speed of air bubbles it is possible to calculate based on equation: ?s = 27.5 * di 1.4 cm/s. Distribution of free surfaces for chalcopyrite is average 80% in the class –74µm +10µm and 20% in the class -10µm. If we get all class sizes, we find that recovery (R) depends from the time by equation:"

Jan 1, 2003

By Cheng Gan, Gui Xiahui, Li Shulei, Cao Yijun, Liu Jiongtian, Wu Lun

Flotation rate constant is an essential parameter in the flotation process. The fine coal sample utilized in this investigation is anthracite from the Shenhuo mine in eastern China. Fine coal flotation rate tests were conducted to compare the flotation rate constant at constant power input with that at gradually increasing power input. Results indicate that the flotation rate constant decreases with the flotation process and increases as the flotation energy is increased. In addition, the flotation rate constant is close to the maximum value. The increasing trend of the flotation rate constant gradually slows down as the flotation energy input increases.

Jan 1, 2014

By R. Imhof, S. E. Sánchez-Pino, H. Sprenger, S. A. Sánchez-Baquedano

"In 1992, Ingeniería de Minerales started with the introduction of pneumatic flotation technology in Chile and South America. This technology consists of vertical cells and gyratory cells, used mainly under actual operational conditions, with pilot units directly installed in the concentrator circuits of the industrial process. Successful industrial applications have been observed at Los Pelambres, in the molybdenum plant; at Codelco Andina in the molybdenum plant as pre-rougher to produce directly a final concentrate; in the copper circuit at Las Luces as pre-rougher producing final concentrate using sea water; at Minera Valle Aconcagua where a full automatic plant produces pre-concentrate from fresh tailings as feed; at the silica and silicate reverse flotation circuit of Compañía Minera del Pacífico; in cleaning the final concentrate of Zn by reverse flotation removing ultrafine carbonate; and in a plant that reprocesses fresh tailings from a copper slag flotation process. Positive operational changes in the design of the flotation circuit have been seen in plants using G-cells and V-cells, improving the performance of flotation circuits and the quality of final products. The high concentration of bubbles and micro turbulence produced by the pneumatic aeration units provide a high probability of collision and attachment, reducing dramatically the residence time. Though it is a pneumatic flotation, no compressed air is needed, and the equipment is characterized by low maintenance costs, full automation, savings in investment and energy."

Jan 1, 2014

By Braulio Fernández, Gonzalo Montes-Atenas

The mechanisms taking place during the leaching of chalcopyrite when it is in contact with other sulphide minerals, particularly pyrite, is still a matter not fully solved. The GalvanoxTM process has been suggested as a technical solution to extract copper from chalcopyrite at commercial level inhibiting passivation phenomena widely reported in the field of hydrometallurgy. Although there are some rules of thumb to implement the process in fully flooded stirred conditions such as the optimum pyrite/chalcopyrite mass ratio should range between 2 and 4, among others; not many research studies have been focused on studying the effect of the surface contact area between chalcopyrite and pyrite to reach best copper extraction conditions. The aim of this research work is to determine the effect of the mass and surface area ratio between the minerals and the surface area of each of the mineral species effectively exposed to the leaching solution. Different particle size distributions of pure pyrite and chalcopyrite were contacted in a small column and subjected to leach tests using sulphuric acid in concentrations close those used in industrial leaching processes. The mass and surface area ratios which optimize the extraction of copper were obtained. It was found the best leaching conditions were attained when reducing the particle size distribution of pyrite regardless the particle size distribution of chalcopyrite. Further analysis concerning the impact of this conclusions on large scale operations is presented and discussed.

Jan 1, 2014

By F. Molhem, S. Banisi, H. R. Montazari, E. Arghavani, Gh. R. Biniyaz, Gh. A. Parsapour

"Water plays a key role in mineral processing plants and to process one ton of ore 2.5 ton water is needed. Thickeners are commonly used for dewatering and recovering water in most processing plants. The underflow pulp density is increased by sedimentation of particles and clear water is recovered from the overflow. One of the issues related with using the process water is the presence of suspended fine particles in the clear overflow water which can create blockage in transfer pipes. The froth formed on top of thickeners is the main cause of this problem. In this study, a method to decrease the froth formed on the Sarcheshmeh Cu-Mo thickener surface was introduced and implemented. At the first stage, the old punched plate feedwell was removed and it was replaced by a vane type feedwell. A spray water ring using fish-tail type nozzles was then installed to break froth layers by water. These modifications led to 63% relative reduction in the water turbidity, 11% relative increase in the underflow solids concentration, 20% relative reduction in torque, 19% relative reduction in its standard deviation and an increase of 6% in water recovery.INTRODUCTION The Sarcheshmeh copper complex, the largest copper producer in Iran, located in southern Iran. In the processing plants of this complex, over 250,000 m3 of water is consumed daily. Because of a lack of water in this area and very low yearly rain fall (150 mm), water plays a vital role in the complex. As a result, it is then aimed at maximum water recovery by taking all necessary measures. The recycled water in order to be used should not contain any suspended solids indicated by low turbidity."

Jan 1, 2018

By Willis Forsling, Prabhakar Swarna, Hanumantha Rao Kota

"The solubility of wollastonite and its Hallimond flotation behavior as a function of dodecylamine concentration and pH are examined. The flotation response is characterized by adsorption and surface energy in the presence of amine. The methods of UV-Visible and FT-IR spectroscopy for adsorption and sessile-drop contact angle for surface energy estimation are employed.The results of wollastonite dissolution clearly showed its non uniform dissolution. The surfaces are depleted with calcium ions and became rich in silicon within 10 min of flotation time. Maximum flotation of wollastonite corresponds to a half monolayer coverage of amine, which is substantiated by the surface energy parameters as shown in figure 1."

Jan 1, 2003

By Sashnee Raja, Mehdi Nemati, Ashley Sissing, Susan T. L. Harrison

"Extreme thermophiles, operating at 65 - 90°C, are finding increasing application in biohydrometallurgy. These micro-organisms have the advantage of exhibiting better oxidation kinetics in terms of reaction rate and extent of mineral solubilisation (Duarte et al., 1993; Norris and Barr, 1988; Konishi et al., 1995). These extreme thermophilic Archae, characterised by a different cell envelope structure (König and Stetter 1986, König 1988, Michel et al. 1980) perceived to provide reduced structural strength in comparison to bacterial envelopes, and customised metabolic pathwaysThe active tank bioleaching process, used for high rate leaching, is conducted in a slurry bioreactor. Here sufficient energy dissipation is required to ensure suspension of the mineral phase as well as to sustain high rates of gas liquid mass transfer. It is well known that subjection to hydrodynamic stress of sufficient magnitude may alter the physiological state of a range of micro-organisms through changed viability (ability of the microbes to grow), metabolic activity and integrity. While limited study on the influence of the solids phase on thermophilic leaching performance is reported, initial reports suggest that the thermophiles used for bio-oxidation appear to be sensitive to hydrodynamic conditions (Jordan et al 1993, Clark and Norris, 1996) and the presence of solids (Norris and Bar 1988, Le Roux and Wakerley, 1988, Escobar et al. 1993, Torres et al. 1995, Nemati and Harrison, 2000)."

Jan 1, 2003

By Derek Caizergues, Hurman Eric

The principle of carbothermic reduction has been around for many years. In principle it is a simple process, yet with a multitude of problems. The temperature required to affect reduction is in the region of 2200ºC and results in aluminium oxy-carbide formation rather than metallic aluminium. From a thermodynamic point of view, reducing the temperatures of reaction which would suppress oxy-carbide formation would only be possible by lowering the total pressure of the system. A decrease in thermodynamic activity of product aluminium by dissolving it in another phase would also help preventing the formation of oxy-carbides and would also increase the yield of the reduction reaction. Thus experiments have been conducted at around 1700ºC to determine the possibility of carbothermic reduction of alumina under the presence of a metallic solvent. Total pressure of the system was reduced to around 30kPa and metallic nickel, iron, copper and tin were selected as the solvent. The highest recovery of aluminium was achieved with the nickel solvent followed by iron, copper and tin. This ranking for the first three was also in accord with the extent of negative deviation form ideality in the respective binary solutions of these solvents with aluminium. The tin-aluminium system displays positive deviation form ideality. The rate and extent of reduction was found to be highly dependent on temperature and pressure. The pseudo first order reaction rate was found to be applicable to the process in all the solvents used. Rate constants were calculated and it is also suggested that the reduction was controlled primarily by the chemical reaction rate.

Jan 1, 2003