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By M. Kosugi, M. Kawata, J. V. Satur, K. Mitsuhashi, R. Kawarabuki, W. Kracht, Y. Ebisu

Copper concentration is becoming more difficult because remaining copper ores are more complex and of finer copper mineral grain size, making copper minerals harder to float because of the fine particle size required to liberate the valuable species. The purpose of this work was to study the flotation behavior of fine copper sulfide ores at different conditions of agitation and aeration. The experimental campaign was carried out in a laboratory Denvertype flotation cell of 1 L volume modified to be operated with forced air that allows decoupling air flow rate and agitation speed. Four ore samples from Chile were used, all of them containing copper sulfides such as chalcopyrite, bornite, chalcocite, and tennantite, but with varying grain sizes and compositions. Preliminary flotation tests for establishing the flotation conditions of grinding size and collector dosage were conducted before the kinetic flotation tests that were carried out at different agitation speeds varying from 900 to 1300 rpm for gas flow rate ranging from 1.6 to 7.2 L/min. The flotation products were analyzed by ICP-MS and MLA (Mineral Liberation Analyzer). The results showed that high agitation speeds with corresponding air flow rates resulted in better recovery than moderate agitation speed and air flow rate, and an excess in gas flow rate resulted in bad performances. The flotation rates of the fine copper minerals were improved despite the different improvement rates among the fine size fractions. The impact of these operational variables, however, was different when comparing the results for the four ore samples. While it was found that the order of floatability in the four samples was the same, that is, chalcocite > tennantite > bornite > chalcopyrite, the kinetic constants of the copper minerals in the samples were different, indicating that mineral composition in the sample affects the flotation kinetics.

Jan 1, 2018

By A. Bastrzyk

Text The mining and refining of minerals generates large amounts of solid waste. The waste from cleaning operations constitutes up to 90% of the total production. Although some of them can be used in mining, civil enegineering, construction, agriculture, most of them must be disposed in dumps and slurry ponds, causing major economic and enviromental problems (Alonso, 2002; Alon-so, 1999). The refuse from minerals cleaning may have considerable valuable particles content, which can be used in industry. Thus, the recovery of these particles from minerals waste by using a cleaning method effective at fine particle size, may overcome these consequences. Surfactants are used in numerous applications including emulsification and solid surface modification. In the oil agglomeration of minerals, the ionic surfactants (both anionic and cationic) are used for the hydrophobization of mineral surface and the oil-water emulsion preparation. When the cationic surfactant is injected into the oil-water mixture, surfactant molecules adsorb at the oil-water interface, changing droplets? properties. The addition of anionic surfactant to the mineral suspension was found to modify the solid-liquid interface. In this paper, the condition and mechanism of selective separation of magnesite from quartz are presented. A satisfactory was achieved with the amount of anionic collector (sodium oleate) equal to 15.2 mg/gsolid and with the amount of cationic collector 27.9 mg/gsolid for cetyltrimethylammonium bromide (CTAB) and 16.9 mg/gsolid for dodecyloammonium hydrochloride (DDAHCl) at pH 8. At these conditions, the amount of agglomerated carbonates was about 12% for CTAB and 5% for DDAHCl.

Jan 1, 2014

By E. V. Manlapig

"Some researchers postulate that the floatability of a particle in the streams of an industrial flotation circuit is a function of only its size and liberation properties. They do not discount the importance of reagent or surface contamination on particle floatability but assume that the reagent coverage or surface contamination of the particle surfaces is essentially uniform for particles of similar size and mineralogical properties when subjected to a particular chemical regime.In this paper, samples collected from laboratory batch flotation tests performed on different streams of Cominco Teck’s Red Dog lead cleaning circuit have been characterised with respect to their size, mineral association and mineral surface exposure. An analysis of this data set indicates that the flotation rate of a particle in an industrial flotation environment is a strong function of its size and also of the mineral composition of its surface (Figure 1). It is a function not only of the proportion of the most floatable mineral on its surface but of the floatability of the other minerals on its surface as well.Nodal analysis is a technique developed by the authors that can be used to determine if the ore floatability of a particle class is changing within an industrial flotation circuit. This technique is used within the paper to show that the floatability of all the different types of particle classes studied within the Red Dog circuit did not change significantly during the lead cleaning stage. However, it was also concluded that particles with the same size and mineral composition did not all float with the same rate in the individual streams of the flotation circuit, but with a distribution of rates. It is suspected that the particles within a size mineralogical class in this study have varying degrees of surface oxidation and that this results in varying particle flotation rates. Thus basing particle floatability on size and mineralogical effects, alone, in a flotation model is not always valid."

Jan 1, 2003

By D. P. Hatfield, G. de Jager

"Recent developments in image analysis techniques and the power of computer hardware have spurred international interest in the potential uses of image analysis techniques in a range of industrial applications. One of these applications is the control of the complex flotation process. Despite years of work, the flotation process is still poorly understood. Current attempts to control flotation cells focus on consistently duplicating the control achieved by human operators.In human control of flotation two of the dominant visual cues are the froth flow speed and the froth stability. These two factors can be measured and inferred respectively from image analysis of video of the froth surface. Two important hydrodynamic variables for control of the flotation process are the air addition rate and the level of the froth pulp interface.The current work focuses on the relationship between froth flow speed and the rate of recovery of concentrate from a flotation cell. Results are presented that show a strong relationship between flow speed and concentrate yield. These results include tests where the conditions in the cell were not changed, as well as tests involving changes to the cell level and air addition rate. Preliminary results are presented which show a correlation between froth stability and froth percent solids.Future developments of the system will include comprehensive froth texture typing, colour space and stability analyses."

Jan 1, 2003

By S. M. Bradshaw, C. Dorfling, F. Ngandu

"Selenium removal and platinum group metal (PGM) recovery from copper sulfate leach solutions form an integral part of platinum producers’ base metal refinery operations. Recent studies found that substantially higher PGM recoveries can be achieved if excess thiourea instead of sulfurous acid is used as precipitation reagent; however, the impact of the proposed process on downstream processes was unknown. The objective of the current study was therefore to investigate the effects that excess thiourea and residual selenium present in the rich copper sulfate electrolyte have on copper electrowinning. This was achieved by performing cyclic voltammetry tests using a platinum rotating disk as working electrode, a graphite auxiliary electrode and a saturated calomel reference electrode. A synthetic copper sulfate electrolyte containing 0.01 M Cu2+, 1 M H2SO4 and varying amounts of selenium (20 – 150 mg/L) and thiourea (10 mg/L and 100 – 300 % excess) was used. The results obtained have shown that both thiourea and selenium interact with the cupric ion cathodic reduction reaction. Thiourea polarized the working electrode and lowered the efficiency of the cupric reduction reaction. Tests on the solutions with high selenium concentration showed simultaneous reduction of copper and selenium, which led to copper selenide formation. Nodule formation on the deposit surface also became significant at higher selenium concentrations. Based on these results, it was concluded that precipitation of PGMs from the copper sulfate solution with excess thiourea is not feasible due to the detrimental effect on downstream electrowinning operations.INTRODUCTION During the high pressure oxidative leaching stage in a typical base metal refinery (BMR) circuit, selenium, tellurium and some platinum group metals (PGMs) are dissolved along with the desired copper ions. The impurities (selenium and tellurium) may pass to the copper electrowinning circuit where it can result in the formation of nodular copper electrodeposits or reduced current efficiency. The presence of PGMs in solution, on the other hand, increases the precious metal inventory and potential losses of the operation. Currently, sulfurous acid is widely used for selenium and tellurium precipitation from copper sulfate leach solutions. Sulfurous acid is capable of reducing cupric ions to cuprous ions; the generated cuprous ions then react with Se4+ and Se6+ to precipitate selenium as a copper selenide (Bello, Dorfling, 2014). Recent studies have, however, proposed the use of excess thiourea as a precipitating agent for the removal of selenium and tellurium; it has the advantage of improved PGM recovery in the Se/Te precipitation step (Lottering, Eksteen et al., 2012; Mulwanda, Dorfling, 2015)."

Jan 1, 2018

By F. Bello, R. Yanez, M. Pinto, T. Errazuriz

"Throughout its operation, Minera Esperanza (ME) will deposit one of the largest tonnages rates of high density tailings in the world with a solids concentration of close to 67% by weight. The tailings presently being deposited have a solids concentration of approximately 62% - 64%, and so cannot be used to directly characterize the flow and deposition characteristics of the higher concentration tailings. To increase the knowledge of the behaviour of their tailings, ME, with the support of Golder Associates, developed a large scale tailings deposition test with a capacity of 30,000 tonnes per day (1,200 m3/h). The test was carried out by depositing tailings into two large cells or paddocks in five stages. Multiple spigots were used to allow different flows to be deposited. At each stage, topographical surveys of the natural terrain and the geometry of the deposited tailings, as well as continuous flow measurement and periodical rheological characterization of the discharged tailings were conducted to create a data set against which beach slope models could be calibrated and then used to predict performance of the higher concentration tailings under different deposition scenarios. This study adopted the beach slope prediction model proposed by A.L. Li (Li, 2011). The model was successfully adjusted to the observations made during this large scale field test by applying the values measured in-situ. This paper presents the application of the model, the results obtained, the findings, and the analysis of possible future scenarios. The model was applied, using the discharge flow rate, the geometrical characteristics of the discharge area, and the rheology with its variation along the beach to estimate the development of the beach formation and the steady state of the beach slopes. Through the use of dimensionless variables, the model was applied to higher solids concentration scenarios, obtaining results that would allow beach slope estimation at different deposition stages in multiple scenarios of varying parameters such as flow, rheology and geometry of discharge area."

Jan 1, 2014

By Vladimir E. Vigdergauz

"Bubble-mineral complexes could be formatted by an attaching of hydrophobic particles to the surface of air bubbles or by an evolution of bubbles from solution onto hydrophobic surfaces. Measurements of contact angles, detachment forces (DF), induction times (IT), evolution pressures (EP) and flotation recoveries (FR) for the studying of minerals wettability at various pH and electrochemical potentials were used. An analysis of the obtained IT results show that a process of bubble attachment to a mineral surface is a rather slow one and it will scarcely be enough for bubble-mineral complex formation under the conditions of real flotation.The ranges of adhesion potentials obtained by DF measurements, Figure 1, correlate with the data of floatability-potential for pyrite. The ranges of adhesion potentials obtained by DF measurements for galena (-1 ÷0.2V) and chalcocite (-0.5÷1.2V) correlate with the potential ranges of floatability for galena (<0.2V) and chalcocite (>-0.4V). An increase of the DF and the cathodic limit of the adhesion potential with increasing length of the hydrocarbon chain were observed. EP-pH curves for sulfides are a mirror-like to the DF-pH curves, Figure 2. Structure of solid-liquid and liquid-gas borders has a determinative importance for formation of bubble-mineral complexes and subsequently flotation results. Under vacuum on the mineral surface there are produced micro bubbles and preferably they will be appeared on the hydrophobic sites. Water structure breaks near a hydrophobic surface facilitate water mass destruction and formation of gaseous phase embryos under decompression in the impeller zone. It simultaneously reduces a probability of produced micro bubbles dissolution as a result of pressure increasing owing to constant fluctuation of liquid densities into impeller zone. Comparison of Taggart’s evaluation of the suction behind blades of the impeller of an agitation-froth machine and ABEP data on galena, Figure, shows that gas evolution will be observed in the range of 1300-2700 revolutions of impeller per minute for hydrophobic and hydrophilic surfaces successively."

Jan 1, 2003

By Glasswell K. Nkonde, Fredrick Chileshe, Steven Simukanga

Improving food security by increasing crop output is a primary objective for most countries in the sub- Saharan region. Most soils in the region are deficient in phosphorus an important nutrient after nitrogen in plant growth. Phosphates are therefore used together with nitrogen and potassium based fertilizers in improving crop production. Zambia like many other countries in the sub-Saharan region imports phosphate fertilizers for use by its farmers. However, indigenous phosphate deposits of igneous origin exist in Zambia of which the main ones are Chilembwe in Petauke district, Mumbwa sugarloaf in Mumbwa district, and Nkombwa Hill in Isoka district. If commercially exploited, these deposits could become a ready source of inexpensive phosphate for the local farming communities in the country. Previous research has shown that partially acidulated phosphate rock (PAPR) produced using Chilembwe phosphate rock is just as agronomically effective as the imported superphosphate fertilizers on food crops in most of the Zambian soils. PAPR is produced by reacting finely ground phosphate rock with only a fraction (usually 50%) of the stoichiometric quantity of the sulphuric acid required to fully convert the apatite in the rock to monocalcium phosphate thus making the process cheaper in terms of acid consumption than the poduction of single superphosphate where the apatite in the rock has to be fully converted to monocalcium phophate. The factors that affect the percentage of available P2O5 in the PAPR produced include particle size of phosphate rock, degree of acidulation, concentration of acid, process temperature profile, residence time and drying temperature. These factors were studied in a 25kg/hr PAPR pilot-plant in the School of Mines at the University of Zambia using Chilembwe phosphate rock. The PAPR pilot-plant consisted of a rotary drum granulator as the main reactor, a rotary drum dryer and a triple deck vibrating screen. Ground phosphate rock was reacted with sulphuric acid and water in the granulator to form a granular product which entered the drier. The dry product was screened into three size fractions. The 1 – 4 mm size fraction was the final product whilst the –1mm size fraction was recycled. The +4mm size fraction was sent to a crusher while the crushed PAPR was sent back to the screens.

Jan 1, 2003

By A. Collings, A. Farmer

Power ultrasound may be used in the processing of mineral suspensions to clean the particle surfaces of oxidation products and fine coatings, mainly through the large, but very localised forces, produced by cavitation. This effect may be utilised in lowering the level of iron contamination in silica sand used for glass making, in improving the sharpness of electrostatic separation of heavy mineral concentrates, in shortening the time of leaching of minerals and in improving the selectivity and recovery of flotation processes. Parameters affecting the efficiency of these processes, such as input power and levels of reagent addition, are discussed. In particular, we present data showing the relationship between power input and the particle size of surface coatings removed, which can be explained by the Derjaguin approximation for the energy of interaction between a sphere and a flat surface. Pilot scale studies, using commercially available components, are currently being used to assess process viability and will be compared with laboratory scale results.

Jan 1, 2003

By M. A. Hampton

The surface oxidation of sulfide minerals in aqueous solutions is an important sub-process in sulfide flotation and hydrometallurgy, but a full understanding of the oxidation process and products is still lacking. Many oxidation pathways and products involving elemental sulfur, metal polysulfide, metal-deficient sulfide and sulfate have been proposed, confirmed and argued. In this paper we provide further insight into the surface electrochemical behaviour of galena in aqueous solutions. For this research we have developed a novel experimental system, that combines chronoamperometry and AC-mode AFM surface imaging, which allows for in-situ, synchronized electrochemical control and examination of oxidative surface morphology. At pH4, the morphology of elemental sulfur (detected by ex-situ Cryo-XPS) formed on the oxidizing galena surface depends on the electrochemical potential pathway. In multi-step chronoamperometry (i.e. four potential steps from 0 mV to + 350 mV) the sulfur forms as nanoscopic domains, whereas in single-step chronoamperometry (i.e. one potential step from 0 mV to + 350 mV) sulfur forms as a heterogeneous layer. In each case the oxidation is controlled so that the number of electrons (coulombs) passed per unit area is the same, therefore the amount of sulfur produced is also the same. The differences in morphology with electrochemical potential pathway are explained using a nucleation and growth model. The formation of sulfur on the surface increased both advancing and receding contact angle of galena, but the morphological changes induced by different electrochemical potential pathways did not significantly alter the hydrophobicity of the surface. Keywords: galena, lead sulfide, oxidation, Atomic Force Microscopy, electrochemistry, collectorless flotation, hydrophobic

Sep 1, 2012

By David Newton, Christian O’Keefe, Robert Maron, Jerin Russell, Paul Rothman, Dylan Cirulis

"The presence of unwanted coarse material in flotation feed streams negatively impacts both recovery and throughput of concentrator plants. The detection of this coarse material is a long-standing problem in mineral processing that has been poorly addressed by existing instrumentation systems. This problem has been overcome by the development of two new systems that detect in real-time the presence of coarse material in the overflow stream of individual hydrocyclones. They both use sensors mounted to the overflow pipe of the hydrocyclone and provide a robust and maintenance-free system measurement that enables corrective actions through operator intervention or automatic control strategies. One system is non-invasive and detects very coarse material 6mm or greater in size. The other system uses a wetted sensor and detects coarse material down to a lower size limit of approximately 100 um. Both systems have been commercially deployed. The systems will be described in detail. Validation data and typical plant data will be shown"

Jan 1, 2014

By A. Boulton

Low molecular weight synthetic polymers substituted with hydroxyl, carboxyl or sulfonate functional groups were used to improve the flotation separation of zinc or copper sulfide minerals from iron sulfide gangue minerals in three massive sulfide ores of different mineral composition. These polymers produced significant improvements in zinc or copper grades as a result of a selective depression of iron sulfide minerals. These results are significant considering the differences in ore type, proportion and type of iron sulfide minerals present, and grinding medium used in this study.

Jan 1, 2003

By James A. Finch, Xiangzhou Ding, Yue Hua Tan

"The Jameson Cell is one of the choices of flotation machine in coal, base metal processing and other specialist applications. This paper determines the effect on vacuum pressure and bubble size of two design variables, orifice size and downcomer length, and the operating variable air-to-water (AWR) ratio. The main findings are: orifice size and downcomer length impact the vacuum but have limited effect on bubble size; AWR < 1 favours high vacuum, conditions are identified where vacuum is maintained at AWR > 1, and water flowrate has slightly greater impact on bubble size than air flowrate.INTRODUCTIONFroth flotation, the most common technique for mineral separation, has been in use for over a century. The process takes advantage of the difference in wettability of mineral surfaces to achieve the separation of valuable minerals from non-valuable minerals, or gangue. Numerous flotation machines have been invented and patented over the years. The Jameson Cell, invented by Professor Graeme Jameson in the late 1980s, is one successful example. First trialed at Mount Isa Mines (Queensland, Australia), Jameson Cells have been installed at operations around the world for the recovery of fine coal (Mohanty and Honakeri, 1999; Cowburn et al., 2006; Hacifazlioglu and Toroglu, 2007; Uçurum 2009), minerals of copper (Farr 1992; Atkinson et al., 1993; Harbort et al., 1997), lead/zinc (Rohner, 1993; Munro, 2003) and gold (Bennett et al., 2012; Lauder et al., 2003), and in water treatment (Yan and Jameson, 2004), solvent extraction de-oiling (Miller and Readett, 1992; Miller et al., 1997; Harbort et al., 2003; Young et al., 2006), oil sands processing (Neiman et al., 2012), and various food industries (Brenneman, 2014). One of the largest units is the 650 cm diameter separation tank with 24 downcomers installed in an Anglo American operation (Osborne and Euston, 2015). Scale up is relatively straightforward: to increase capacity the number of downcomers is increased with corresponding increase in size of separation tank.The Jameson Cell comprises two main parts: a vertical tube (downcomer) which provides self-aspiration and intense bubble-particles contact, and a (separation) tank where particle-bubble aggregates disengage from the pulp. The intense bubble/slurry mixing in the downcomer with air holdups reaching 60% (Marchese et al., 1992) accelerates particle collection enabling the greatly reduced cell volume compared with mechanical flotation cells and columns. The disengagement of the particle-loaded bubbles from the slurry in the separation tank is usually aided by addition of washwater."

Jan 1, 2018

By C. H. Veloso

"Starch is the most widely used depressant in the reverse cationic flotation of iron ores. There is however, an indication from recent studies, that other polysaccharides may successfully replace them. When starches are used in the flotation of iron ores in the presence of quartz as gangue mineral, their strong adsorption on the surface of iron oxides can be explained by the molecular conformation between the available sites on the mineral surface and two hydroxyls of starches. However, when the gangue minerals are iron-bearing silicates, the strong interaction with starch can occur on these minerals since they have the same surface behaviour as iron oxide. In this work bench scale tests were conducted in order to generate scientific knowledge about other alternatives depressants for the flotation of iron ores. A magnetic pre-concentrate from a skarn iron ore processing plant was used as feed material for flotation tests. The reverse flotation approach was used to upgrade the iron content by removing complex ironbearing silicates. The depressants used in this study were: corn starch, dextrin, carboxymethyl cellulose (CMC) and humic acid. The tests were performed under different pH conditions in order to try to relate the efficiency of depression to the pH used during flotation. The results show the important role of pH as each depressant reached its best performance at different pH values. At alkaline pH the corn starch showed best depression performance while the humic acid is more efficient at pH close to neutrality.INTRODUCTIONIron corresponds to approximately 6% of earth’s crust composition (McDonough and Sun, 1995). It is the most used metal in our lives, some of its properties as resistance and facility to be shaped makes is replacement very difficult. The primary sources of iron on our planet are minerals. The iron-bearing minerals most commonly found in nature and economically exploited are magnetite [Fe3O4], hematite [Fe2O3], goethite [FeO(OH)] and siderite [FeCO3] (L O Filippov et al., 2014). These minerals are commonly associated with other minerals (most of the time not economically exploited) forming the so-called iron ore. Iron ore is the source of primary iron for the world’s iron and steel industries."

Jan 1, 2018

By Hideki Yamamoto, Norihiro Murayama, Junji Shibata

"Hydrothermal syntheses of zeolite from coal fly ash were carried out by using various alkali sources. NaOH, Na2CO3, KOH, K2CO3 and their mixture were applied for an alkali source of zeolite synthesis. The various physical properties of the reaction product, such as the kind of zeolite crystal, cation exchange property, surface texture and so on, was investigated through the zeolitization reaction from fly ash. The mechanism of zeolitization reaction was considered from these results.Zeolite P(NaP), hydroxysodalite(HS) and chabazite(K-CHA) are synthesized as zeolite species, when fly ash hydrothermally reacts in various alkali solutions at 393K. The crystal structure of the products obtained in NaOH solutions for 3h changes from NaP to HS with increasing NaOH concentration. K-CHA formation in KOH solutions needs 10h of reaction time, which is longer than that of NaP or HS.Dissolution, condensation and crystallization steps exist in the zeolitization reaction from fly ash, and the particle surface of products remarkably changes in each step. The fly ash is spherical particles and the surface is smooth(Fig.1(a)). The dissolution of fly ash occurs in the heating process until 393K, and the particle surface changes like unevenness(Fig.1(b)). In case of NaP, the condensation of aluminosilicate ions takes place at 373-393K, and the amorphous aluminosilicate is deposit on the unreacted fly ash(Fig.1(c)). The crystallization of NaP already begins to occur at 393K and the surface is covered with fine zeolite crystals for 24h(Fig.1(d))."

Jan 1, 2003

By Gurubasayya Swamy

This paper presents the performance study of sag mill in the processing of gold ore. Deterioting ore grade and high demand of metals has tremendously influenced the SAG mills. Today?s high capacity Semi-autogenous grinding (SAG) mills expand vast amounts of energy and in doing so consume tons of shell liners and steel balls, while processing ore. Semi-autogenous (SAG) mill performance is influenced by ball charge, feed properties, shell, grate, and pulp lifter design. In the performance study of SAG mill, based on the results obtained it can be observed that SAG mill performed better at feed size +4 inch and grinding media consumption 0.90kg/mt. In the present study the effect of crusher bypass on SAG mill performance, an immediate drop of throughput ranging from 10-20tph is observed. Keywords: sag mill, pulp lifters, grinding media, energy, consumption, throughput

Sep 1, 2012

By S. V. Petrov

Oxidised ores possess a significant share among raw materials which are treated by traditional plant technology. As usual, the chemical composition of these ores is rather simple. They can be treated by standard cyanidation. In this case, the resulting wastes have an alkaline reaction. Their toxicity (in case of ROM ores treatment) is mainly due to the presence cyanides and thicyanades. The tails are dexotified before disposal. However, chemical reagents used cannot provide a complete removal of toxic matters. In this case, this disposal poses a real problem because these tails contain a significant amount of CN and SCN and their behavior during a long disposal should be studied. A sample with a simple composition taken from cyanidation tails was studied. The sample presents itself the quartz low-grade sulfide gold-bearing ore. Sulfide sulfur content is 0.15 per cent,and heavy metals content is 0.023 per cent. Method of testing is described further. The samples were tested under moderate and subarctic climates based on the difference in temperature, moisture and the degree of oxygen saturation of air. The pH of water extract, which was prepared using distilled water, was also determined besides measuring the concentration of cyanides and thiocyanates. This demonstrates the stability of sulfide-bearing minerals in the disposed tails. The tests time was 820 days. It was found that the alkalinity of the samples tends to lower under oxygen-containing conditions in proportion to temperature increasing. Under conditions without oxygen, the pH lowering is minimal. Mineralogical and chemical properties of the ore material give positive alkaline balance during testing. The solid sample contains enough alkaline agents to compensate dangerous to the environment reactions of sulfides oxidation.pH value maintaining under alkaline conditions witnesses to the possibility of a safe disposal of this tails type. The largest amount of cyanide is removed under acid-containing conditions at positive temperatures. The higher the temperature is, the more intensive destruction is. At the moment, of finishing the tests at 20ºC temperature, the residual concentration of CN- was 0.06-0.10 mg/L, at 4ºC, the residual concentration of CN- was 0.2-0.3 mg/L and at -18ºC was 0.4-0.6 mg/L. Under conditions with the lack of oxygen, cyanides can be removed within the first 200 days. Then, this process fully stops. A stabilized cyanides concentration is 3.0-4.0 mg/L. The presence of sulfides increases the content of cyanides at the initial stage of testing. Then, the concentration of SCN at the temperatures above 0ºC decreases rapidly under oxygen-containing conditions. At the rise of temperature, a narrowing of peak at the curve and an increase of the destruction process are observed. At the end of testing, the concentration of thiocyanates in the moisture of wastes was 0.2-0.3 mg/L at the temperature of 20ºC and 0.5-0.6 mg/L at the temperature of 4ºC, respectively. The concentration of thiocyanates contained in a frozen sample and media which have the lack of oxygen stabilizes at a certain level owing to sulfides and does not practically change further. It was found that detoxification of oxidized cyanidation tailings with a simple composition which were disposed as filtration cakes can be possible. In this case, the concentration of cyanide in the moisture of disposed wastes can have a close value or equal to actual concentration during cyanidation. In order to meet the requirements of high ecological safety standards and successful detoxification process of toxic compounds in the tails under the action of natural factors, the conditions of air aeration with oxygen for the whole volume of tails are required. Keywords: cyanides, thiocyanates, storage, detoxification, flotation cakes

Sep 1, 2012

Opportunities to monitor and control primary grinding mill performance are strongly sought after in the mineral processing industry. Currently, limited on-line information about mill charge motion and content is available to mill operations for control purposes, leading to periods of lower throughput, instability, variable product size and accelerated mill liner and lifter wear. In response to this need, CSIRO has developed an on-line surface vibration monitor for primary grinding mills which produces data that has been shown to provide new information about the mill charge in terms of toe and shoulder position, as well as potentially key features such as the overall charge level, the distribution between rock and balls in the mill, and the impact of the charge on the mill liners and lifters. This paper outlines the key features of the on-line monitor system, particularly those relating to data transmission, data analysis, and the design of the monitor and its independent power supply. It describes the coupling of single vibration sensor data from the CSIRO on-line monitor to the actual operating conditions of a SAG mill and how the vibration response and hence mill operating conditions vary as a function of time, including during mill equipment failures such as a broken discharge grate. Opportunities for improved mill control based on the data from the on-line monitor are also discussed, as well as the implications in terms of mill processing and maintenance performance. Recently a CSIRO monitor was also installed on a ROM ball mill and analysis of the vibration sensor data from this installation is currently underway. Preliminary findings from this installation will be presented along with comparisons of generic information, such as toe position (measurement precision and operation variability) and vibration signal (intensity, sensitivity and operation variability), between this type of primary grinding mill and AG/SAG mills.

Sep 1, 2012

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 Achilles Dutra, Everton Santos, José Oliveira

The beneficiation of phosphate ores by froth flotation is the most efficient process used to separate apatite from gangue minerals like calcite, dolomite and quartz. However, the similarity of surface properties between apatite and calcite generally lead to non-selective adsorption of reagents, rendering the selective separation of these minerals a worldwide problem. The phosphate deposit of Itataia, State of Ceará, Brazil, studied in the present work, presents a complex mineralogical composition having uranium associated with the apatite mineral. The main gangue minerals are calcite and quartz. The bulk flotation of apatite and calcite with anionic collectors in an alkaline medium followed by the selective flotation of calcite at pH 5.5 using phosphoric acid as well as citric acid as depressant have been suggested for this ore. This paper presents the results of contact angle measurements obtained using jojoba oil, a natural reagent composed mainly of gadoleic acid (C20:1) and long-chain fatty alcohols (eicosenol and docosenol), as an alternative collector for the selective separation of apatite and calcite minerals. The hydrophobicity studies were carried out using a computer controlled contact angle goniometer. Additionally, the collector adsorption was evaluated via electrophoretic mobility and FTIR measurements. The results indicated that a high selectivity can be obtained by using jojoba oil as collector in a slightly acid pH range, without the use of depressant. The best results were achieved with a jojoba oil concentration of 200 mg.L-1 at pH 6.5, where the apatite was fully hydrophilic and calcite showed a high hydrophobicity (? > 60 º).

Jan 1, 2014