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By Kazutoshi Haga, Batnasan Altansukh, Shirchinnamjil Nyamdelger, Atsushi Shibayama, Narankhuu Ariunbolor, Gunchin Burmaa

In this study, the authors investigated the capability of an acidic thiourea solution and silicon-organic polymers (PSTM-3c, PSTM-3T) as ion-exchange resins to recover of gold from gold-bearing ore concentrates. Firstly, elemental gold present in flotation concentrates was dissolved by leaching with a solution of nitric acid and thiourea under the optimized conditions. The best result on gold thiourea leaching was obtained under a nitric acid concentration of 2 N, thiourea concentration of 2 %, and oxidant (Fe2(SO4)3) concentration of 3 %, solid:liquid ratio (S:L) of 1:20, leaching time of 6 hours at 20 °C with a gold recovery of 93.7 % for a gold flotation (unroasted) concentrate. For the roasted gold concentrate, the dissolution of gold was 94.8% under the optimized leaching condition as nitric acid concentration of 0.5 N, thiourea concentration of 2 %, and the oxidant concentration of 1 %, S:L ratio of 1:10, leaching time of 4 hours at 50 °C. Secondly, a series of sorption tests was carried out on a pregnant leach solution containing gold complex Au[S=C(NH2)2]2+ using silicon-organic polymers (PSTM-3c and PSTM-3T), respectively. The effects of solution pH, adsorption time and temperature in the sorption process are also studied. As the results, the PSTM-3c and PSTM-3T polymers were adsorbed about 94.4 % and 95.1 % gold from the pregnant leach solutions under the optimum sorption conditions, respectively. It was found that the both PSTM-3c and PSTM-3T polymers were effective for the recovery of gold from the pregnant leach solution of thiourea. Adsorption activity of the PSTM-3c and PSTM-3T polymers was confirmed by new peaks near 1700 cm-1 in the FT-IR spectrum of the gold-adsorbed polymers, respectively.

Jan 1, 2014

By Glaser. C., J. Balz, F. Logsch, R. Heiduschke, M. Leiker, P. Ay

The treatment of iron-hydroxide-containing water from ground water and surface water is achieved by a combination of the process steps of flocculation and subsequent mechanical dewatering. The aim is to create solid pellet structures by extending the structure forming flocculation process with a build-up pelletizing process which can be transferred directly into a drying unit. A Taylor-Couette-reactor (diameter of the inner cylinder – 40 mm, gap width – 5 mm) was used for these experimental studies. To produce the necessary flow profile the inner cylinder was rotated at a speed of 230 rpm. The iron hydroxide-containing suspension (dry matter content: 2 mass %) was added simultaneously with the addition of a cationic high-molecular flocculant in various flocculant dosages and residence times of 5 to 15 min. The pellets were examined for parameters such as geometric dimensions, dry substance content and dewatering behaviour. As the results show, there is a direct relationship between the residence time and the geometric dimensions of the pellets. After a residence time of 5 min, round pellets with an average diameter of 6 mm were formed. With an increase in the residence time up to 15 min, a compaction of the pellets could be observed, which resulted in an increase in the dry substance content of 8.0 to 11.2 mass % on average. After completion of the pelletizing process, the pellets were mechanically dewatered by filtration. By applying this innovative wet pelletizing of iron-hydroxide containing suspensions in a Taylor-Couette-reactor, it is possible to carry out the process of flocculation combined with the pellet formation with simultaneous pellet compaction in a single process step. The resulting pellet structures are distinguished from conventional floc structures by an improved water discharge capacity. After classification the pellets can be marked directly as easy-to-handle bulk material, suitable as feedstock in percolation columns for the purification of contaminated fluid streams

Jan 1, 2018

By A. V. Kozub, D. O. Sharkovsky, R. I. Ismagilov

"Due to complex mineral composition and fine ingrained nature concentration of iron ores deposited in Mikhailovskoye mine field requires application of wet magnetic separation to produce 65–66% Fetotal and 8.2–8.6 %SiO2, concentrate with 90–94% of material being –0.044micron grain size. Higher specific consumption of ROM, increase of production costs with concurrent reduction of output - those are inevitable side effects of desired concentrate grade improvement. Large-scale complex analysis and surveys have been carried out aimed at concentrate grade improvement with concurrent output increase. Classification of feed in hydraulic cyclones (hereinafter referred to as hydrocyclones) has been the bottleneck for improvement of processing throughput and concentrate output. Hydrocyclone classification efficiency is 50-60% and further improvement is practically impossible. Actual circulating load may achieve as much as 500-600% while the optimal rate is 200-250%. Application of wet fine screening has been considered to improve iron ore concentrate grade. Objective of this work is to design processing flow diagram for unoxidized ferruginous quartzites with implementation of wet fine screening. Large-scale tests have been run in Crushing and Concentrating Plant with application of wet fine screening stage. These tests included application of wet fine screening in 2 and 3 stages of classification to separate desired grain sized material; replacement of hydrocyclone classification with fine screening; application of fine screening as additional stages to concentration process and screening of final concentrate. Testing Methods. EXPERIMENTS AS WELL AS THEORETICAL RESEARCH HAVE BEEN APPLIED FOR THE PURPOSES OF THIS WORK; INCLUDING MAGNETIC, GRAIN-SIZE AND CHEMICAL ANALYSIS OF CONCENTRATION PRODUCTS. MODERN ANALYTICAL DATABASE HAS BEEN APPLIED TO STUDY WET FINE SCREENING FEATURES, MINERAL AND PHYSICAL COMPOSITION OF CONCENTRATION PRODUCTS. Work Results: - analysis of wet fine screening application for iron ore concentration. - technological solutions enabling to improve slurry classification of fine ingrained low magnetic iron ore have been developed. - effective process flow diagram including fine screening has been designed based on the feasible and reasonable arrangement solutions."

Jan 1, 2018

By I. H. Mukhametshin, E. N. Baranova, I. B. Fadina, E. A. Ashirbaeva

The purpose of the research is the development of a complex of solutions for the maximum extraction of non-ferrous and precious metals from persistent mineral raw materials by heap bioleaching from spent heap leaching (HL) stacks. Methodical recommendations for assessing the suitability of primary and technogenic refractory mineral raw materials for heap bioleaching are developed. Active associations of microorganisms have been created for the conversion from various types of ores to the solution of S, Fe, As, Sb, Cu, Zn, Mn, Ni, Mg, P and other elements, as well as methodologies for their storage, immobilization and preparation of bioreagents in industrial conditions. On a pilot scale, tests were carried out on samples weighing 15-17 thousand tons of refractory gold-sulphide ores (more than 50% of gold is associated with sphalerite), gold-quartz ores with colloidal gold (74% associated with quartz and pyrite) and gold-silver ores with elevated copper and zinc content (1.5 and 3,5%, respectively), as well as man-caused material lying for 4-5 years of spent quarry material of oxidized gold-silver ores. In the pilot-industrial tests of heap bioleaching of gold-sulfide ores, gold recovery of 84-85% and silver was achieved to 89-90%, the possibility of obtaining high-yield solutions of copper and zinc, suitable for hydrometallurgical processing, from gold-silver ores, and the possibility of obtaining waste with a dump content of valuable components, suitable for deep disposal in the construction industry. When comparing two technologies for processing refractory ores after biooxidation under HL conditions, when 1000 tons of ore processed by the bioreagent were re-milled from a size of 40 mm to 0.1 mm and cyanated under the conditions of the factory process, the same results were obtained for gold recovery (85%) and silver (90%), as with the heap version. The copyrights of the development are protected by a patent.

Jan 1, 2018

By J. Yvon, Inna V. Filippova

"The aim of this work is to seek the inhibitors of the meteoric and bacterial dissolution of sulphides and gangue minerals to stop the undesirable chemical reactions during conservation of the flotation wastes. The approach of passivation of surfaces by chemical treatment of the solid phase is applied for this objective.The samples taken from different depths of an old French waste dump revealed the capacity of the flotation tailings to produce acid waters (pH 1.8-2.4) and to release heavy metals. Mineralogical studies show not only the product of sulphide oxidation, i.e. sulphates, but also the complex transformations of aluminosilicates in acidic liquid phase. The detection by XRD of aluminium hydroxides (gibbsite, boehmite) allows supposing the recrystallisation phenomena during tailings conservation.Comparative tests of the passivation of the surface of sulphide minerals and waste of flotation with using of conventional reagents (CaO, NaOH, phosphates) and original reagents for this purpose (alkyl dithiocarbamates) allow to identify the optimal treatment conditions and the efficient chemicals.Leach tests were carried out in percolation columns during 68 weeks. The normalised leaching tests according to French legislation were run to confirm the selected treatment conditions. The results obtained show that a single treatment with carbamate inhibits the oxidation of the pyrite and the other sulphides, and totally prevents the formation of acid waters (the stabilised pH was 5.3-5.8). Treatment of in situ drainage water allows to obtaining a total precipitation of heavy metals: the residual concentrations of Fe, Cu and Zn are lower than 0,1 mg/l.The passivation of sulphides is the result of the formation with carbamate (studied by IR spectroscopy and XPS) of organometallic compounds, which are stable in acid medium. The presence of thiuramdisulphide (product of alkylcarbamate oxidation) at the mineral surface stabilises the mixed adsorption layer and leads to a considerable reduction in the hydratation rate of surface by avoiding the corrosion of the pyrite. No aluminium was detected in leach solution with this treatment."

Jan 1, 2003

By M. Özer, G. Önal, F. Arslan

"The use of ultrasonic in industrial processes has increased during the last few years. Ultrasonic vibrations are used in sieving, grinding, ore washing, cleaning, and flotation in mineral industry. There are also some attempts for the utilization of ultrasonic treatment in separation and removal of fine particles from gases and liquids. In Kalemaden A.S. (Turkey) four different types of clay mixtures (1. A mixture of clays from Balikesir-Düvertepe and Istanbul-Sile, 2. A mixture of clays from Ukrania and Balikesir-Düvertepe, 3. Sögüt-Kadikelimesi, 4. A mixture of clays from Sögüt and Istanbul-Sile) and kaolin from Balikesir-Düvertepe (Turkey) are concentrated before their use in ceramic production. Dewatering is the important step in those types of concentration plants. Sedimentation of concentrated clay has always been difficult and taken long times due to their nature and having small particle sizes. Flocculants can be used to enhance the sedimentation, but they are not preferred by the ceramic industry since they affect the quality of ceramic products. For this purpose, ultrasonic treatment is used in the sedimentation of clays mentioned above for solving the problems encountered related to the ceramic industry and promising results were obtained.Kaolin sample, subjected to this experimental study, from Balikesir-Düvertepe region of Turkey was brought from the plant as a pulp in containers and throughly mixed with a stirrer before sedimentation experiments. A two liter graduated cylinder and an ultrasonic bath (with 25 kHz frequency and 0.5 KW power) were utilized in the tests. Superfloc A-120 (1% concentration) was used as a flocculant. The settling distance was reported against the settling time during the experiments. Initial and final pulp densities were also determined. The effects of several parameters such as pulp density, flocculant addition, and ultrasonic treatment on the sedimentation of kaolin were investigated and the results are represented in terms of settling distance versus settling time."

Jan 1, 2003

By Gülay Bulut, Mustafa Özer, Yunus Emre Benkli, Olgaç Kangal, Istanbul Technical University, Mustafa Tarkan

"Zeolites are naturally occurring as hydrated aluminosilicate minerals. They belong to the class of minerals known as “tectosilicates” and are related to the common minerals feldspar and quartz. Seven natural zeolites that occur in large, commercially exploitable deposits, are: clinoptilolite, chabazite, mordenite, phillipsite, erionite, analcite, and ferrierite. Among them, clinoptilolite is the most abundant one and is not the best known, but is one of the more useful natural zeolite. Clinoptilolite [(Na3K3) (Al6Si30O72) 24 H2O] is very closely related to heulandite and is currently being considered for disuse it self as it may just be a variety of heulandite. It differs from heulandite significantly only in its enrichment in potassium and slightly more silica and it is argued that a separate mineral is not needed.There are large zeolite deposits in western part of Turkey. The sample used in this study was taken from the Gördes region of these deposits. Screen, chemical, XRD and mineralogical analyses were used to determine properties of the natural zeolite sample used in this work.According to the size distribution of the sample, it is found that the zeolite sample used in this study is below 1 mm in size and almost 80% of it is below 0.5 mm. X-Ray Diffraction (XRD) and mineralogical analyses show that the natural zeolite is found to be in the forms of clinoptilolite and heulandite. Clinoptilolite forms as a devitrification product of volcanic glass in tuffs. Quartz, clay minerals, orthoclase, plagioclase, biotite, seruzite-muskovite and epidote were observed as impurities. XRD analysis also shows that the sample contains approximately 58-60% clinoptilolite, 5% quartz, 5% feldspar, 10% smectite, 5- 10% illite and mica and remaining volcanic tuffs. Several types of mineral processing methods were performed in order to remove impurities from the natural zeolite sample to produce high purity zeolite. Gravity separation methods such as shaking table and superpanner were carried out for separating heavy minerals, while high intensity dry magnetic separation was used for discarding magnetic minerals."

Jan 1, 2003

By Stephen Simukanga, Jewette Masinja

"Mining has been going on commercially in Zambia for over 100 years. The backbone of the mining industry has been copper production and its by-products of cobalt and gold. Over these years, the mining industry ownership structure has swung from private ownership to state ownership in 1972, and back to private ownership in 1995. Environmental management was first introduced into the body of Zambian legislation in 1991 through the promulgation of the Environmental Protection and Pollution Control Act (EPPCA). The Act’s main functions included the protection of the environment and control of pollution, and in particular to provide for the health and welfare of the people, animals, plants and the environment in general. This Act, was replaced in 2011 by the Environmental Management Act (EMA). The new Act has a number of new elements including: mainstreaming environment in national planning, it provides for the domestication of multilateral environmental agreements, enhances public participation issue, creates a central environmental information depositary, elaborates access to information principles, establishes an environment fund, creates enforcement orders, provides for both Zambia Environmental Management Authority and members of the public to sue for damages following environmental pollution, and provides for the appointment of honorary Inspectors. In addition to this, the Mines and Minerals Act of 1995 provided, for the first time, a section on environmental management in the mining sector. This section also created the Environmental Protection Fund (for mining), and made it obligatory to undertake environmental impact assessment before mining permits could be issued. The Environmental Protection Fund has now been established, as provided for by the law, and currently has more than USD9.0 million in the account. Secondly, environmental auditing is now being carried out annually on mines around the country, the effect of this has been a significant improvement in the environmental management of mining in Zambia. This paper looks at the response of the Zambian mining sector to these pieces of environmental management legislation, and the direction that the mining sector is expected to take on environmental management going forward."

Jan 1, 2014

By A. D. Shuloyakov, G. A. Finkelstein, V. I. Kurets, A. K. Vedin

"In disintegrating solid ores with mineral values disseminated in them, one of the principal tasks is to selectively separate valuable mineral particles from the matrix in which they reside, striving at the same time to keep their natural shape and size as intact as possible.The conventional mechanical disintegration methods do not meet this most important requirement in full. The other major objective here is to reduce electric power consumption during the fragmentation stage, since up to 65 per cent of the total power consumption at concentrators processing ores of non-ferrous, ferrous, rare, and precious metals is spent on disintegration steps.Numerous experiments conducted on dozens of ore types (tin, tungsten, and many others, as well as on rock containing diamonds, rubies, emeralds, etc.) have invariably demonstrated by far superior integrity of mineral values as compared with that obtained by mechanical as well as other types of disintegration.However, the process remains as power-intensive as ever which is due to the imperfect nature of the electro-technical devices that convert the network electric current into high-voltage electric impulses responsible for the disintegration process.The maximum capacity attained in disintegrating the hardest materials from 40 mm to 2 mm size in a single operating chamber with four high-voltage electrodes does not exceed 1.0-1.5 t/h. Attempts at increasing the number of electrodes and the capacity of the operating chamber have failed so far because of high overall dimensions and mass of the electrical part of the installation supplying the chamber with pulsating current, as well as of the commutation requirements. At the same time, a number of overseas operations have reported a significant breakthrough in their attempts to reduce dozens of times the overall dimensions and mass of the discharge impulse generating installation (EIS), which enables us to contemplate to increase the capacity of the EIS at least ten times in the nearest future. Yet, even with the currently achieved capacity of the EIS, these installations have found wide use in geological surveying, precious and semi-precious stones production, in grinding super hard materials, etc., since they provide spectacular selectivity of disintegration and thus the integrity of valuable mineral crystals."

Jan 1, 2003

By R. Weyhe, B. Friedrich, H. Heegn

"Nickel-metal hydride batteries (Ni-MH) are storers of electrochemical energy, which have a higher specific storage capacity than lead or nickel-cadmium batteries. The demand for Nickel-metal hydride batteries is increasing rapidly since their market launch in the early 1990's. In 1999 the output of cells exceeded 80,000 tons per year (1 billion cells per year). Today there is no suitable and sustainable recycling process to recover nickel, cobalt and rare-earth metals. The discarded batteries are used in the steel industry as alloy material because they contain nickel. Cobalt and rare-earth metals are lost; they are non-recycleable.In a German governmental funded research project, IME Aachen, ACCUREC Mühlheim and UVR-FIA Freiberg are cooperating in processing as well as in creating a feasibility study. The target of this project is the development of a new recycling process for metal recovery from Ni-MH-batteries. The proposed process consists of a combination of mechanical, pyrometallurgical and hydrometallurgical processing steps.After shredding the steel shell, the various fractions of battery materials are carefully separated by mechanical processing. A hammer mill with one rotor with a perforated discharge grid of 20 mm opening, was found to be suitable for crushing the batteries to release the active mass of electrodes for metallurgical processing. The ground material is wet screened at a mesh size of 0.5 mm; thus a fine fraction is obtained with valuable components such as Ni, Co, and RE and an oversized fraction consisting of a mix of iron chips, electrodes grids, plastic chips, paper, and flocculent material of separators. The organic components are avoidable when there is a thermal step at the beginning of processing batteries.The separated fine fraction is smelted in an electric arc furnace. Any pyrometallurgical process relies on a suitable slag system. In this specific case, the process has to allow separation of nickel and cobalt as metal from the rare-earths almost quantitatively, collecting the rare-earths as well as impurities e.g. as oxides. The products are a nickel-cobalt alloy and a slag phase enriched with rare-earth oxides for further treatment to ‘mischmetal’."

Jan 1, 2003

By Bertil I. Pålsson, Sture V. Persson, Kent T. Tano

"Autogenous (AG) and semi-autogenous (SAG) mills often operate in an unstable state because of the difficulty to balance the rate of replenishment of large ore particles from the feed with the consumption in the charge. This has led to an increased interest in obtaining an accurate and direct measurement of mill load and the behaviour of the mill charge. A problem in attempting to measure those parameters is getting a sensor that is both robust and sensitive enough for continuous on-line measurement.Techniques that measure the force acting on the lifter when it hits the charge inside the mill have got an increased interest recently because of the ability to combine it with DEM modeling. This paper presents a method for the measurement of the apparent filling level in a pilot ball mill equipped with the Metso Continuous Charge Measurement system (CCM). In this technique a strain gauge sensor is mounted on a flat steel spring which is fitted into a recess underneath a lifter bar. In addition, a conductivity probe, the Boliden Grinding Measurement System (GMS), is mounted in another lifter bar with the purpose of comparing the two measurements. To visualise the behaviour of the charge a 2D DEM modelling technique is used with Metso HFS software.The pilot mill is a grate-discharge mill, equipped with 12 rubber lifters of square size 0.1 m, face angle 45 degrees. Steel balls in the size range 10-30 mm and density 8000 kg/m3, are used in the experiments. Test material is a hematite pellet feed, d50 around 45um, chosen to get stable grinding conditions with respect to feed size variations.The experiment is meant as a first test of the equipment’s performance, and to study how the sensors respond to changes in some operating variables. To get an understanding of, and distinguish between correlation and causality, experiments are performed according to a full factorial design with two levels, and in addition two replicates of the experiments at a center-point in the charge level setting."

Jan 1, 2003

By Andrew T. McBride, Malcolm S. Powell, Indresan Govender

"Current empirical Semi Autogneous Grinding (SAG) mill models contain assumptions concerning the amount of energy available for particle breakage, how this energy is distributed in the mill media and the rate at which the energy is transferred. Despite these assumptions the JK SAG model is highly functional with a proven track record. DEM provides a numerical framework to greatly improve on these assumptions that were necessary due to a lack of available input data.This paper identifies key outputs of the Discrete Element Method (DEM), such as energy spectra and impact probability distribution. It describes how they can be incorporated into current mill models utilising practical rock breakage data. The rate at which energy is transferred is shown to be dependent on particle position and mill rotational speed and not once per cycle as previously assumed. Based upon this an improved energy transfer methodology is presented. The fundamental outputs of the DEM are validated against experimental three-dimensional particle tracking data, so as to establish whether the DEM produces correct energy transfer predictions on the inter-particle level, which is crucial to this work. • Effective Experimental ValidationAn automated 3D tracking technique is employed to study the motion of plastic particles deep within the charge of a 142mm diameter experimental mill. A Biplanar Angioscope is used to film the mill with X-rays in two planes simultaneously at 50 frames/s, with a shutter speed of 1/3000s. A marked ball within the charge is tracked for over 2 minutes and the resulting digital images processed by a fully automated imaging technique, which locates the 3D coordinates of the particles to within 0.2mm. With over 250 circulations, this provides statistically rigorous and accurate data for verification in the numerical modelling of mills.A series of validation techniques have been developed to compare the experimental trajectory data with the outputs of both 2D and 3D DEM simulations. The techniques describe the shape of the charge and the particle motion within mill, allowing objective comparisons to be made of key features of the charge, such as the equilibrium surface and the centre-of-circulation."

Jan 1, 2003

By I. Blayda

The purpose of this work is to study and make comparative analysis of germanium extraction and related valuable components of the sublimates from the burning of domestic power coals (product 1) and germanium sulfide materials, which are a waste of lead-zinc production (product 2), by traditional chemical methods (distillation of germanium in the form of tetrachloride from raw and preliminary burning source) and by microbial bioleaching of sulfur-oxidizing bacteria. The dependence of the germanium extraction by chemical methods from phase composition of the initial raw materials was installed. The germanium tetrachloride extraction from products 1 and 2 were 78.50 and 19.52%, respectively. Such difference in indexes on extraction, is caused by germanium confinement as concomitant trace component to the basic phases to carriers. The share of acid-non-soluble compounds (tetragonal modification GeO2 and silikogermanaties) in the product 1 account for 21.5 % of germanium. Ratio between acid-soluble and acid-not -soluble germanium forms are 19.52 and 80.48 %, respectively, in the product 2. Our experiments have shown, that implementation of restorative firing (with addition of 30-40 % carbon at 1150 0?) of sulfide product 2 considerably impacted on the extraction of germanium tetrachloride (91.76 %) in comparison with its low enough extraction at straight distillation of hydrochloric acid (19.52 %). The results are confirmed by a set of physical methods. The results of processing the same so-called hard phase?s material (product 2) with the help of microorganisms are presented. It Has been established, that selected strains of bacteria are capable of extracting from initial raw materials not only macro components (iron, zinc, lead, manganese, aluminum, nickel), but also micro impurity of rare metals (gallium, germanium, zirconium). It is important that these metals were not extracted by traditional chemical methods (with application of aggressive conditions and heats) independently of the phase composition of the source. Almost complete extractions of germanium in solution using sulfur-oxidizing bacteria take place in the first day of the process independently of the phase composition of the source and the type strain. The results have practical significance and can be the basis for developing a unified biotechnological method of technogenic waste processing with a purpose of their sterilization and detoxification with simultaneous obtaining concentrates of valuable metals. Keywords: germanium, extraction, sublimates, bioleaching, sulfur-oxidizing bacteria.

Sep 1, 2012

By Buks Kruger

"After the milling and flotation of the platinum bearing ore, the flotation concentrate is electrically smelted in 6-in-line electric arc furnaces and the resulting furnace matte treated in Peirce Smith converters to remove the iron sulphide. The iron free (less than 1% Fe) converter matte is then granulated and sent to the Base Metals- and Precious Metals Refineries for further processing.During the smelting and converting processes two distinct gas streams are produced.The Peirce Smith converter off gas contains 4% - 9% SO2 which is treated in a conventional Sulphuric Acid Plant to produce sulphuric acid (H2SO4).The electric furnace off gas contains 0.9% SO2 and was (until September 2002) vented through a 91 meter high stack to atmosphere.Off gasses which contain less than 3% SO2 is difficult to handle and quite a few processes had been developed over the years to cope with this gas. A broad spectrum of process suppliers and technology approaches is available and the different technologies can be divided into a few main approaches i.e.Scrubbing of the off gas with an alkaline solution to produce an environmentally friendly and stable waste product which can be discharged onto a tailings dam or permanent landfill site.Physical absorption of the SO2 into a chemical solution to produce high quality chemically pure process chemicals.Catalytic reaction of SO2 with O2 to produce SO3 which is absorbed in water to produce sulphuric acid of less than 90% strength.In October 2002 Impala Platinum commissioned a Sulfacid Plant at its Smelter in Rustenburg which recovers the SO2 from the electric furnace off gasses into a weak sulphuric acid solution.The Sulfacid Plant technology is widely used in the paint pigment industry. This is, however, the first application of the technology on electric furnace off gas.The furnace off gasses contains flue dust which is removed in electrostatic precipitators. The gas exiting the precipitators normally still contains between 40 mg/Nm3 and 60 mg/Nm3 dust and passes through a quench-scrubber before entering the reactors. The quench-scrubber cools the electric furnace offgas down from ± 200 °C to 60 °C and act as a final dust removal stage."

Jan 1, 2003

By Raquel Franco de Souza Lima, Isao Matsuoka

"Microflotation studies and abstraction experiments were conducted with synthetic oxide spinels relating to chromite (MgCr2O4, FeCr2O4, FeFe2O4 and FeAl2O4), using sodium oleate as collector. An attempt was done to correlate this data with the speciation of oleate in the bulk solution and at the interface solid-water, to explain the floatability curves. The microflotation tests were conducted using a microflotation cell. The abstraction of sodium oleate was measured at 25°C, with one gram of synthetic spinel and the abstraction time was 30 minutes. After centrifuging, the residual oleate concentration in the supernatant was measured by using the spectrophotometric method described by Mizuniwa et al. (1977), that covers the range from 1.5 to 9 ppm. To cover the range from 0.2 to 1.5 ppm, the residual oleate concentration was measured using the spectrophotometric method described by Gregory (1966). The amount of oleate abstracted was calculated from the difference between initial and residual (equilibrium) concentrations.Figure 1 shows the floatability of FeCr2O4, FeAl2O4, FeFe2O4, MgCr2O4 as a function of pH and sodium oleate concentration of 1 x 10-5 M. The IEP of each sample is indicated in the figure by a vertical line in the horizontal axis. The chromium-bearing spinels FeCr2O4 and MgCr2O4 show the lowest isoelectric points (IEP), around pH 6, while in the case of FeFe2O4 and FeAl2O4, the isoelectric points lie at pH 6.5 and 7.3, respectively. It is seen that the flotation-pH curve for FeFe2O4 has a peak at the pH of the IEP, while flotation peak for FeCr2O4 appears at pH below the IEP and that of MgCr2O4 does at pH above the PZC. On the other hand, FeAl2O4 is floated at pH range between about 4 and 7,3 (IEP). This suggests that the pH value at which the maximum flotation occurs is dependent on the sort of spinel to be floated, though it appears in the vicinity of the respective IEP."

Jan 1, 2003

By Haghi. Hamed, Javad Vazifeh Mehrabani, Mehdi Sedigh

In this investigation, the possibility of physical separation methods such as attrition scrubbing, hydro-cycloning and also reverse flotation were investigated for silica and calcite removal from relatively low grade kaolin. The head sample was provided by the Iran China Clay Company and the major oxides contained in the head sample were Al2O3, SiO2, CaO and Fe2O3 with grades of 15.07%, 71.05%, 4.35% and 0.52% respectively. The liberation degree of calcite and iron impurities from kaolin particles were over 80% for particles finer than 210µm and 53µm respectively. Attrition scrubbing tests were carried out with scrubber cell of the conventional Denver flotation cell model D-12. Laboratory scale hydro cyclone was applied for the beneficiation of kaolin. Attrition scrubbing tests with control screen of 106µm did not achieve the desirable yield for purification of this kaolin sample, but hydro cyclone experiments resulted in better results. Hydro cyclone with 2.54 cm diameter used and the only variable was the cyclone inlet pressure ranging from 68.65kPa to 98.07kPa. The best inlet pressure was found to be 68.65kPa. Based on the optimized condition, Al2O3 and CaO amount in the hydro-cyclone overflow was 23% and 1.47% respectively. However weight recovery of the overflow in each cyclone experiment was less than 30% and multi stages of hydro-cyclones would have to be applied for higher weight recovery and better yield. All of the flotation tests were carried out in the conventional Denver flotation cell model D-12. Reverse floatation tests for calcite removal were carried out under alkali pH based on full factorial design of variables in 2 levels including one center point. The three parameters tested were collector dosage (gr/ton), pH and depressant dosage (gr/ton). The collected data from flotation tests were analyzed and optimized collector and depressant dosage were 1000 gr/ton and optimized pH was 8.5. Under the above mentioned conditions, calcite removal was about 75% and CaO content in the final product was reduced from 4.35% to 1.33%. However calcite removal will increase to more than 83% if the feed particle size in flotation tests is reduced from 210µm to finer than 53µm. Finally after optimization, the best working condition and possible flow sheet were developed.

Jan 1, 2014

By R. ?. Sherembayeva, ?. ?. ?uktybayeva, ?. B. Rakhimbekova, N. ?. ?m?rova

"Studying the interaction of the phosphorus-containing flotation reagent with the components of the flotation system ""liquid-gas-solid"" during flotation of non-ferrous metal ores allows regulating the enrichment process. The phosphorus-containing reagent-collector anabasinium-O,O-dimethyl-thiophosphate has beensynthesized under laboratory conditions and the concentrated aqueous solution of anabasin hydrochloride and the 40% solution of sodium hydroxide have been used as the raw material. The phosphorus-containing reagent has been obtained by interaction of the anabasine base, sulfur and dimethyl phosphite, due to sulfur and nitrogen atoms it can form complex compounds with heavy metal ions.Studying flotation of copper-sulfide ore of the Sayak field with the use of the phosphorus-containing reagent-collector anabasinium has been performed in the open and closed cycles. The degree of ore grinding was 60- 62% of the class -0.074 mm. There has been established the dependence of the ore flotation parameters on: a) pH of the pulp; b) the consumption of the reagent-collector anabasinium.The effect of the pulp pH on the technological parameters of copper ore flotation has been carried out with a reagent regulator that increases the difference in the surface properties of the minerals to be separated.There has been used lime as the regulator of the medium, the consumption of which varied from 750 to 1500 g/t; the consumption of the reagent-collector anabasinium was 10, 15, 20 and 25 g/t.It has been found that when flotation of copper ore without the use of lime at pH equal to 7.8 and at the reagent consumption, g/t: anabasinium - 25, T-92 - 55, copper recovery in the concentrate is 92.72%, the quality of concentrate is 7, 1%.In flotation according to the factory mode (the consumption of xanthate is 44 g/t, T-92 is 55 g/t, pH = 7.8 (without lime)) of copper ore, copper recovery in the concentrate is 87.38%, the concentrate quality is 7, 97%, with reducing the xanthate consumption to 25 g/t copper recovery is reduced to 83.39%, the quality of the concentrate is up to 6.69%.In the experiments using the factory reagent mode in the closed cycle, with the xanthate mass consumption of 44 g/t, T-92 blowing agent of 55 g/t, the third recleaning concentrate contained 19.13% copper with recovery of 86.89%.Using a phosphorus-containing reagent instead of xanthate with the same flow rate, the third recleaning concentrate with the mass fraction of copper of 19.82% has beenobtained with recovery of 87.77%."

Jan 1, 2018

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 Hiroshi Sasaki, Herman D. Mendoza

"The surface-chemical property of nickel slag fiber was modified in aqueous media in order to act as an active and efficient collector of colloidal amorphous silica from geothermal effluent. Colloidal amorphous silica (0.05 µm) from geothermal wastewater causes operational and ecological problems. It clogs geothermal pipes and waterways, and when disposed to the environment poses hazardous effects on both the flora and fauna ecology. Because colloidal amorphous silica is extremely fine and remains in suspension in aqueous media, conventional solid/liquid processes to remove colloidal silica from its bulk liquid are rendered ineffective.A rapid separation technique is then developed to remove effectively amorphous colloidal silica from its bulk liquid by attaching the extremely fine particles of silica onto a nickel slag fiber coated with magnesium hydroxide, Mg(OH)2. The nickel slag fiber has the following characteristics: a high surface area and predominantly possesses negative charge in aqueous media with an iso-electric point at pH ~2.5. When soaked and saturated with Mg(OH)2 solution, the surface of the nickel slag fiber becomes coated with fine and compacted Mg(OH)2 precipitates. This modifies the surface- chemical property of nickel slag fiber transforming the negatively charged surface into a positively charged surface in aqueous media with an iso-electric point of around pH 11.8, which corresponds to the iso-electric point of Mg(OH)2. When geothermal effluent containing negatively charged colloidal amorphous silica particles (i.e.p. of silica is pH 2) is passed through a column-bed packed with surface-chemically modified nickel slag fibers under natural pH conditions, the colloidal amorphous silica particles are recovered by attachment onto the surface of the surface- modified nickel slag fiber. The recovery of colloidal amorphous silica by attachment is 97-99%, resulting in the production of a relatively clean and silica free output. Aluminum hydroxide, Al(OH)3, was also used to modify the surface –chemical property of the nickel slag fiber. In the same way, it also exhibited a positive response with the collection of colloidal amorphous silica from its bulk liquid, but yielding a lower recovery of 90%. This may be attributed to the lower surface potential and iso-electric point of pH 9.3 for Al(OH)3. The separation process was evaluated and analysed using existing potential energy theories. Figure 1 shows a micrograph of the surface of an unmodified and the Al(OH)3 –modified surface of nickel slag fiber."

Jan 1, 2003

By M. L. Torem, R. H. Rojas, A. G. Merma

"Fine particle recovery by conventional flotation processes is very low mainly due to the low probability of bubble/particle collision and adhesion. In order to solve the problem of low particle recovery, several flotation technologies have been developed to increase bubble/particle collision efficiency. Among these technologies, the electroflotation process stands out. This process has advantages in the generation of microbubbles (<100 µm) and in the production of different amounts of hydrogen and oxygen microbubbles. These advantages favorably influence the fine particle floatability, due to the greater probability of particle/bubble collision and adhesion. The electroflotation tests were conducted for a hematite/sodium oleate system in a Partridge-Smith modified electroflotation binary cell of 0.38 L usable volume. The sodium oleate concentration, particle size, pH and current density were evaluated. Satisfactory results in the recovery of hematite were found at pH values of 7, reaching hematite floatability of 99% and 90% with hydrogen and oxygen bubbles, respectively.INTRODUCTIONThe flotation recovery of fine and ultrafine particles is normally very low and is caused by several factors, among them, the low probability of collision and adhesion bubble-particle, the difficulty to overcome the energy barrier (entrainment and entrapment), low selectivity, surface oxidation and mineralogical changes (Schulze et al., 1989; Waters et al., 2008; Shahbazi et al., 2010). This problem can be overcome by decreasing the bubble size or by increasing the apparent particle size. However, it is worth noting that the use of small bubbles or micro bubbles also involves some disadvantages such as their low momentum resulting in a slower process comparing with conventional flotation. Electroflotation is an attractive alternative for treating fine particles with small bubbles less than 100 µm, generated by the electrolysis of water. Electroflotation is one of the variants of the flotation process, where the gaseous phase is produced by electrolysis of an aqueous solution, generating oxygen and hydrogen bubbles (Sarkar, 2010; Gupta and Ali, 2012). These smaller size bubbles allow the recovery of fine particles by increasing the collision efficiency. This process is versatile and competitive in relation to other techniques such as dissolved air flotation and dispersed air flotation because the electroflotation units are smaller, more compact and require less maintenance and less operating cost than other flotation units (Zouboulis and Matis, 1995,). In addition, the electroflotation process is a clean technique and provides results in a short time, requiring only the investment in the electroflotation cell construction stage and the choice of the electrodes (Ketkar et al., 1991; Sarkar et al., 2010; Sun et al., 2011). In this sense, this study assesses the effect of pH, particle size and sodium oleate concentration on electroflotation of hematite fines."

Jan 1, 2018