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By P. Saha, D. M. Chakrabarti, National Metallurgical Laboratory, P. Bhattacharyya, B. R. Sarkhel

The estimated reserve of the phosphatic soils at the Sukulu hills region of Uganda upto a depth of 60 meters is of the order of 200 million tonnes and analyses 10-12% P2O5. A 5-tonne sample of the phosphatic soil was received at the National Metallurgical Laboratory (NML), India for beneficiation studies. The ore occurred as a naturally degraded soil deposit and the slime contained earthy lateritic minerals which made it extremely sticky. Microscopic examination revealed the presence of limonite, magnetite (martitised), hematite and goethite as major minerals along with apatite and quartz. Presence of clay was indicated by earthy smell on moistening the sample. It was observed that getting rid of the slime was as important for adequate beneficiation of the ore, as it was difficult. Earlier studies on samples of the same ore at the NML and abroad established that it was necessary to pass the ore through a series of three stages of desliming, each consisting of a step of rigorous attrition scrubbing followed by hydrocycloning, for effective elimination of the sticky slimy coating which stubbornly adhered to mineral grains. Studies were carried out at the NML in two phases to develop a flowsheet for beneficiation of the phosphatic soil. In the first phase, reproducibility of the results obtained by employing a flowsheet developed abroad was confirmed along with suggesting some modifications of the flowsheet. Then 200 kg. of concentrate was produced following the recommended flowsheet for evaluation of its suitability for production of fertilisers. To remove the limonitic slimy coating, which stubbornly adheres to the other mineral grains, it was necessary to subject the ROM ore, after screening out the +840 micron size fraction which contained only 1.75% P2O5 , to three stages of hydrocycloning each preceded by attrition scrubbing. Then only conventional beneficiation techniques could be effectively employed to upgrade the ore.

Jan 1, 2003

By M. Ghiani, R. Peretti, S. di Giovanni, G. Zonnedda, A. Serci

"An interesting occurrence of gold bearing ores of economic interest has recently been discovered in the Serrenti- Furtei district, central-southern Sardinia (Italy). The upper part of the orebodies are leaner and fairly porous, and are undergoing intense oxidation processes. In the lower parts sulphide ores predominate, chiefly enargite-luzonite and pyrite and these have a more compact structure. The passage from the oxidized to the sulphide zones, is rather irregular and difficult to delineate. The gold, generally occurring in its native form, is found in small grains. Mineral reserves in the area concerned were originally estimated to total 2.77 Mt: 0.63 Mt of oxide minerals with average gold content of 2.75 g/t and 2.14 Mt of sulphide ores with average gold grade of 3.18 g/t.Recovery of the valuable metals is a complex problem.The effectiveness of a variety of gold extraction techniques has been evaluated conducting tests on batches of ore representative of the different orebody depths obtained from core samples.The techniques investigated were: heap and vat leaching; flotation and flotation followed by leaching of the flotation tailings. The findings indicate that:• the gold contained in the ores in the upper oxidized zones of the deposit can be efficiently recovered by direct cyanidation via heap or vat leaching;• the sulphide ores in the deeper portions, that are not amenable to direct cyanidation but contain enargite concentrations of potential economic interest can be processed by means of flotation to produce a gold/copper bulk concentrate;• beneficiation of the difficult-to-treat minerals contained in the transition zone requires some knowledge of their intrinsic properties. A distinction should be made between the ores containing minor amounts of enargite which appear to be amenable to vat leaching and those with relatively higher enargite content which are processed using bulk flotation of the gold and copper minerals followed by vat leaching of the resultant tailings."

Jan 1, 2003

By Olgac Kangal, Ali Guney, Gulay Bulut, Guven Onal, Ayhan A. Sirkeci

"This paper presents the results of pilot scale column flotation applications in the two different copper concentrators in Turkey. The Kure Copper Plant is located in the Black Sea Region of Turkey. There are four types of copper ore formations in the Küre region. The so called disseminated ore contains 60-70% siliceous minerals of which Cu content is around 0.5%. The remaining three ore types in the region are generally named “massive ores”. The massive ores may assay up to 15% Cu and the major gangue mineral is pyrite associated with relatively little amount of silica. The main copper mineral in all formations is chalcopyrite that is generally finely disseminated in pyrite therefore satisfactory liberation requires ultrafine grinding especially in the case of the massive ores.A blend of these ores, containing 1.7% Cu on average, is fed to the Küre Copper Concentrator whose capacity is 1.2 million tons of ore annually. Unfortunately, today the plant operates below its designed capacity treating around 550,000 tons of ore per year. The design of Küre Copper Plant was undertaken by the Outokumpu Company of Finland. The operation of the plant is almost automatically controlled and the feed, the concentrate and the tailings are assayed for copper by on-line XRF analysers. The particle size analysers are also connected to the grinding circuit. The feed material is ground almost below 50 µm and the flotation is conducted around pH 11.2 using Hostaflot X-231 (a trade mark of Hoechst) as the collector. Apart from the rougher cells, there are four cleaning stages after which the final concentrate is produced. A very fine grinding requirement for an adequate level of liberation makes successful flotation difficult and consequently the final concentrate can hardly assay above 16% Cu leading to copper losses around 20% in the tailings that contains 0.3% copper."

Jan 1, 2003

By O. N. Mohanty, S. Mohan Rao, N. D. Rao, T. Mukherjee, P. V. T. Rao

"Chromite ore is an indispensable raw material in the manufacture of ferro-chrome and charge-chrome, which are used for the production of stainless and other alloy steels. The demand for chromite ore is ever increasing because of increasing consumption of these steels. Keeping this in view, Tata Steel is keen to recover values from fines and wastes, and also to produce value added products from their captive chromite mines and its processing plants.Tata Steel has its captive chromite resources at Sukinda, Orissa. They contain two ore types, i.e. (i) Ferruginous and (ii) Siliceous. The generation of off-grade ores is an increasing trend and simultaneously customer quality requirements are becoming ever more stringent. The ferruginous type ore also contains a considerable quantity of in-situ fines (~20% particles below 0.5 mm) that compound the beneficiation problem.In many places, in India and abroad, mined non-marketable off-grade and low grade chromite ores are upgraded by using either simple classification techniques like screw classification, hydrosizing, hydrocycloning or conventional gravity concentration processes such as Heavy media separation, Jigging, Spiraling, Tabling etc.At Tata Steel, the ferruginous type ores are treated in Chrome Ore Beneficiation (COB) Plant that comprises: a crushing and grinding circuit; a classification circuit using hydrocyclones; and a beneficiation circuit using 4 stage spirals in the coarse circuit (-0.5+0.1 mm) and 3 stage spirals & tables in the fine circuit (-0.1+0.038 mm). In this process, 3 types of tailings are being generated and together analyses about 17 % Cr2O3, which is high. From the present operation the chromite recovery is around 70% and could not produce coarse concentrates (+0.5 mm size). Whereas the siliceous type ore is treated in the Lumpy Ore Processing (LOP) plant, consisting of crushing-washing & classification-hand sorting operations, to produce marketable grade lumpy ore and –10 mm de-slimed fines. These fines are intermittently treated in the COB plant. The higher silica content (greater than 1%) and low Cr/Fe ratio (less than 2.8) are the problems with these concentrates."

Jan 1, 2003

By Xin Tan, Changgen Li

"The floatabiliby of chelate CF-collector for zinc and lead oxide minerals was described. It found that CF-collector possesses a strong collection power for zinc and lead oxide minerals as well as excellent selectivity for the gangue minerals. A new technology of zinc and lead oxide flotation with CF reagent as a collector, lead nitrite as a activator and water glass as modifier was presented. The mechanism of interaction between reagents and minerals was discussed by means of adsorption, zeta potential, nephelometric titration, XPS and infrared spectra was investigated.CF-collector, newly developed by Beijing General Research Institute of Mining and Metallurgy (BGRIMM), is a kind of chelate collector for the flotation of oxide minerals. CF-collector mainly consists of N-nitroso-N-phenylhydroxylamine ammonium salt. The CF-collector was used for the selective flotation of scheelite in the Chinese plants.In this paper, the effects of the dosages of activator Pb(NO3)2 and depressants (sodium hexametaphosphate, polyphosphate, water glass and salified water glass) on the floatabilities of several minerals (cerussite, smithsonite, calcite, dolomite, limonite and quartz) as well as their mixtures were investigated in the presence of the CF-collector. The results show that the CF-collector is the excellent collector for selective flotation of cerussite and smithsonite. Pb(NO3)2 can selectively activate the oxides of lead and zinc resulting in a decrease of the CF-collector dosage. The sodium hexametaphosphate plus the salified water glass are the effective depressants for gangue minerals. Based on the above facts, the “CF process”, namely, used CF reagent as a collector, Pb (NO3) 2 as a activator, and sodium hexametaphosphate plus salified water glass as depressant, has been used for the flotation separation of the lead oxide mixtures or zinc oxide mixtures without disliking and heating. For the feed lead assaying 19.07%, the lead concentrate assaying 49.81% Pb at the recovery 80.69% was obtained after one step flotation. For the feed zinc assaying 12.85%, a zinc concentrate of assaying 29.56% Zn at recovery 83.87% was obtained."

Jan 1, 2003

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 Jean-Paul Franzidis, Robert G. Coleman, Emmy V. Manlapig

"The Floatability Characterisation Test Rig (FCTR) is a self-contained, highly instrumented mobile pilot flotation plant developed by the Julius Kruttschnitt Mineral Research Centre, the Mineral Processing Research Unit of the University of Cape Town and EIMCO, as part of the Australian Minerals Industries Research Association (AMIRA) P9 Project. Apart from being a fully operational pilot plant, the FCTR was designed to determine flotation model parameters and to develop and validate flotation plant modelling, scale-up and simulation methodologies.The FCTR was installed at WMC’s Kambalda Nickel Operation where circuit modelling, simulation and scale-up test work was performed using the AMIRA P9 flotation model as the basis of the analysis. The model parameters were obtained through metallurgical sampling, batch flotation tests and gas dispersion characterisation around the FCTR. Model parameters were determined for four FCTR circuits, each of increasing complexity. The circuits ranged from a simple rougher-cleaner configuration with no recycle streams, to a more complex rougher-cleaner-recleaner configuration with two recycle streams.Using the P9 modelling methodology, the system was analysed using four mineral species: nickel sulphide, iron sulphide, copper sulphide and non-sulphide gangue. The floatability of each mineral was analysed as two floating species (fast and slow) and a non-floating species. Mass balanced data from all four FCTR circuits were regressed simultaneously together with data from 47 batch flotation tests. Nonlinear regression was used to determine the solution. The model fit was found to be accurate with most data points predicted within experimental standard deviations. A Monte Carlo sensitivity analysis was also performed to establish the stability of the regressed parameters.Using the P9 simulation methodology, simulations of five FCTR circuits (different from the previous four) were performed. The FCTR was also operated in these five circuit configurations to obtain experimental data to validate the simulated predictions. The simulations were found to predict the recovery and grade of nickel sulphide and copper sulphide within experimental standard deviations. The prediction of recovery and grade of iron sulphide and non-sulphide gangue was less accurate. Overall the FCTR simulations predicted the changes in circuit configuration well."

Jan 1, 2003

By Sanggono Adisasmito

"The quality of the higher education in Indonesia is being improved by implementing a program financed by the World Bank under a project named QUE (Quality for Undergraduate Education). The investments are provided to selected study programs through a competitive selection process. The grant finances staff development, the purchase of equipments, textbooks, consumables, technical assistance, and incentives for outstanding faculties such as teaching grants, project grants, lecture note awards, and educational policy studies. These additional investments are provided to produce chemical engineering graduates that will compete beyond the national market.Chemical Engineering Department of Institut Teknologi Bandung in Indonesia has been selected to receive the QUE grant beginning the year 2000 and ending the year 2004. The department is actively involved in the mineral processing issues, particularly in the aspects of energy supply and the environmental protection. The activities are distributed in different laboratories and areas of expertise, such as: thermodynamics and utility systems, process equipment, chemical reaction and catalysis, microbiology and bioprocess engineering, process control, ceramics, as well as polymer and membrane technology. The main objectives of the QUE project are to improve the undergraduate program in the following aspects: Relevance, Academic atmosphere, Institutional management and commitment, Sustainability, as well as Efficiency and productivity, or abbreviated as RAISE. At the end of every fiscal year, the progress of the program is evaluated to measure the effectiveness of the project.The achievement of the QUE project objectives were assessed using performance indicators developed during the program design. There are six indicators to measure the performance of the individual program of study, such as: (1) Admission Test score, (2) average students' Grade Point Average (GPA), (3) average graduates' length of study, (4) graduates' waiting time before getting first job, (5) Test of English as Foreign Language (TOEFL) score, (6) Graduate Record Examination (GRE) score. Essentially, the RAISE evaluation criteria will be used to perform three main functions, such as (1) to measure the achievement through the six quantitative performance indicators, (2) to support the progress of evaluation and reporting throughout the implementation of the program, (3) to provide a universal framework for qualitative evaluation."

Jan 1, 2003

By Markus A. Reuter, Jacques J. Eksteen

"The modelling of bath type furnaces tends to be either fundamental in nature or total empirical ""black box models"". While models of the first kind are robust, they tend to lack accuracy, in cases where they are to be used for process control, and may take an overly long in development time. On the other hand, black box models tend to lack robustness of prediction for all circumstances and tend to be limited to interpolate based on historical data. While this may very often provide short-term accuracy, the models may have problems with stability in the long term. Moreover, the model structure may not reflect any of the fundamental properties of the system and remains opaque to fundamental analysis. The aim of the model development is in obtaining a model that have robustness, high accuracy, a short development time and which is adaptive to a changing environment. The models are specifically developed for on-line decision support or control of furnaces. The modelling approach is evaluated for a chromite bath smelting furnace. The role of systems analysis, mass balance smoothing, thermodynamic analysis are integrated into one generic algorithm for bath type furnaces. Not only are fundamental process relationships such the mass and energy balances satisfied through a scientific method of data reconciliation; the proposed modelling approach allows adaptive prediction, the first step towards predictive control or metallurgical decision support.It is shown that neither an ARMAX model only, nor a purely equilibrium model only, could predict the dynamics of the process very well. However, a combination of the two approaches more than doubled the accuracy as measured by the R2. It was noted for carbon dissolved in the alloy, that the improvement in R2 in using a hybrid modelling approach was more than the sum of the R2 of the individual traditional approaches. Similar improvements in modelling performance were noted for all other species.It shows further that process dynamics may totally overshadow the effect of thermochemical equilibrium (even when the thermochemical equilibrium prediction includes the recycled alloy and slag heels as additional feeds). The exclusion of process dynamics therefore leads to erroneous results."

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 A. N. Zagorodnyaya, T. N. Bukurov, Z. S. Abisheva, A. S. Sharipova

"This work presents the results of the development of a flowchart for the processing of copper production dusts resulting in the production of of lead sulphate, tribasic lead sulfate (TBLS), ammonium perrhenate, zinc, copper-cadmium cake.Dust having the following composition (wt. %): Pb 39.3, Zn 6.5, Cu 5.5, Stotal 10.8, As 1.05, SiO2 0.6, Cd 0.8, Bi 0.04, Ag 0.02, Re 0.03 was used in the work. Chemical and X-ray analyses indicated that lead, zinc and copper are generally present in dusts in the form of sulfates, various amounts of oxides, sulfides, silicates; sulfur (according to chemical analysis data) is present in the form of sulfates (~ 90%) and in the form of sulfides (~ 10%).Studies have been made on two-stage stripping of copper production dusts containing lead, zinc, copper, cadmium, rhenium in the form of various compounds, at first with soda solution, then with nitric acid solution. It has been indicated that the combination of the operations allows the recovery of 98% rhenium, 82% lead, 92% copper, and 96% zinc and cadmium each in the solution. Furthermore, at the stage of dust leaching with soda, 80% of rhenium and 0.01% of nonferrous metals each are recovered in the solution. Remaining quantities of all metals are recovered in nitric acid solution up to maximum values. Such behaviour of metals is caused by metal phase content in dusts and properties being formed during leaching of compounds. At the stage of dust leaching with soda solutions, carbonates with various compositions are formed due to the exchange reaction between nonferrous metal sulfates and sodium carbonate. The conversion of PbSO4 into PbCO3 is apparently occurs in the solid phase and the conversion of readily watersoluble zinc, copper, and cadmium sulfates into that of carbonate salts occurs in the liquid phase. Rhenium passes into solution due to the presence of rhenium greater quantity in dust in the form of readily soluble perrhenate. Some portion of the perrhenate is, probable, blocked by lead sulfate and liberated in the conversion of PbSO4 into PbCO3."

Jan 1, 2003

By S. K. Kawatra, T. C. Eisele

"Coal-fired electrical power generation plants produce 56% of all the electricity in the U. S., burning approximately 860 million tons of coal annually. This results in production of 58 million tons of fly ash; 19 million tons of bottom ash and boiler slag, and 23 million tons of desulfurization sludges. These are a considerable disposal problem, and it would therefore be very valuable to be able to sell these residues and byproducts as useful materials, rather than paying to dispose of them in landfills. However, utilization rates are currently very low, below 32% even for the most thoroughly commercialized combustion byproduct (fly-ash). This poor utilization rate is a result of the high impurity content of combustion byproducts, which make them unsuitable for existing markets. The experiments described in this paper were therefore carried out to study the application of mineral processing techniques to upgrading combustion byproducts.Experiments were conducted to upgrade and purify low-grade combustion products to produce highgrade, readily saleable materials. A process was developed for removing unburned carbon from coal fly-ash by froth flotation, using reagents originally developed for flotation of oxidized coals. This technique could reduce the carbon content of fly-ashes containing up to 11.1% carbon to less than 2%. The froth product was sufficiently carbon-rich that the recovered carbon has value as fuel, or as low-grade activated charcoal.Fly ash was also examined as a binder for producing iron ore pellets, primarily as a substitute for bentonite. It was found that Class F fly ash in combination with an activator (calcium hydroxide) was an effective pellet binder at dosages comparable to the currently-used dosages of bentonite clay. While the flyash worked very well alone, tests in combination with bentonite showed that fly-ash/bentonite mixtures had significantly worse binding performance than either pure bentonite or pure fly-ash-based binder. This was determined to be due to the fact that bentonite and fly ash have profoundly different binding mechanisms, with fly-ash undergoing a pozzolanic chemical reaction while bentonite binds through a physical attachment process."

Jan 1, 2003

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 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 Arkady Senchenko, Sergey Rybkin, Svetlana Lagutina, Alexander Aksenov

"The application of autoclave leaching technology for sulfide concentrates containing base and precious metals is spreading nowadays. In the process of concentrate leaching silver accumulates in the forms of jarosite compounds, transforms into passive chemical state and is mostly found in solid phase. Effective technology development for silver recovery from solid phase of concentrate autoclave leaching raises the necessity for comprehensive research of silver forms of occurrence and their properties in this product. The possible form of silver presence in solid phase of concentrate from autoclave leaching is argentojarosite. This article is about the study of physical and chemical properties and structure of synthetic argentojarosite - AgFe3(SO4)2(OH)6. A method of argentojarosite synthesis has been developed under conditions simulating the process of autoclave leaching of sulfide concentrate, and includes silver dissolution in the form of Ag2SO4, Fe3+ sulfate hydrolysis, AgFe3(SO4)2(OH)6 build-up. X-ray data of synthesized argentojarosite completely correspond to those of natural mineral. The structural formula of this complex compound has been studied and confirmed. The chemical properties of synthetic argentojarosite, its solubility in acids and alkalis have been investigated. Phase changes when heating argentojarosite with the build-up of iron oxide and silver sulfate stop at the temperature equal to 650 ºC. Based on the results received the technological solutions for solid phase of autoclave leaching of concentrate have been developed with silver recovery of 95-98%."

Jan 1, 2014

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 John Starkey

"The development of the SAG Power Index (SPI) Test in Canada has created a new and accurate way to measure ore hardness in a SAG environment. Coupled with the standard Bond Ball Mill Work Index Test it is now possible to determine from these two relatively inexpensive laboratory tests, the amount of energy required to grind an ore from the primary crushed size to the desired liberation size. By testing multiple samples to discover where the hard and soft ore zones are located, the representative hardness distribution for the ore body can be determined and grinding equipment selected that is capable to meet production targets for all mining areas of the deposit.Previously, it was deemed prudent to select up to 50 t samples of ore for Semi Autogenous Grinding (SAG) pilot plant tests and a second 5 t sample for metallurgical pilot plant work. The methods outlined in this paper show how the 50 t sample is no longer required for SAG design because it is better to measure the representative hardness distribution of the ore body than the hardness of a “chosen” representative sample. This is demonstrated to be true by the fact that the lower horizons of an ore zone cannot initially be accessed to recover 150mm pieces, and the bulk samples taken, rarely represent the desired design hardness of the ore. Median hardness will not yield a good result in most cases and a clear understanding of the location and extent of the hardest zones is imperative to achieve a truly successful grinding circuit design.This paper discusses two plants (Kubaka and Agnico Eagle) that have been designed using SPI and Bond with no pilot plant test backup. Both have been very successful in that they can grind design tonnage on the hardest ores in the mine. This guarantees that the mine’s profitability is protected in any mining sequence. It also allows the extra power to be converted to higher throughput on softer ores if additional cash flow is needed. The advantages from the owner’s point of view are dramatic. This procedure will be attractive as well when considering the costs for test work, and the samples for testing. Existing diamond drill core is normally used and this allows the inclusion of data from the deepest regions of the mine. In addition, it is also clear that the decision to use a crusher can now be made at the design stage of a project based on measured parameters and the estimated capital costs of alternative designs."

Jan 1, 2003

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 Zoran M. Stevic, Mirjana M. Rajcic-Vujasinovic, Zvonimir D. Stankovic

"Covellite is one of the most important copper sulfide minerals. Its behavior during the anodic polarization, as well as its rest potential in various solutions are of importance for flotation processes and also define the mechanism of electrochemical extraction of copper from sulfide minerals.Measurements of the rest potential have been performed in water solutions in presence of different cations and anions. The existence of the Nernst type dependence of the rest potential on the activity of some of the investigated ions was established. The biggest influence on the rest potential of covellite exhibits the change of activities of the ions forming the crystal lattice of investigated mineral, i.e. Cu(II) and S(II). The dependence of the rest potential of covellite on logarithm of Cu(II) activity has a shape of a strait line with a positive slope of 60 mV, while when concentration of S(II) anions increases ten times, the rest potential of covellite decreases about 120 mV. The first dependence was established in acid medium, while the second was registered in alkali one.Different electrochemical techniques have been used for the investigation of the behavior of covellite during anodic polarization. In the basis of all these measurements is a three electrode system consisted of: 1) working electrode made of the sample of natural covellite from the Bor mine (Eastern Serbia, Yugoslavia); 2) reference electrode (saturated calomel electrode) and 3) counter electrode (flat platinum). Electrolyte solutions used in these investigations are of the same kind as those used in the rest potential measurements. Sulfate and chloride solutions, as well as the mixed sulfate/chloride solutions, are the most perspective from the application point of view.Cyclic voltammetry has been the first used method that confirmed the formation of passive layer on the electrode surface during anodic polarization. Elementary data about the reaction mechanism have been obtained too. More detailed data needed for more precise conclusions about the mechanism and rate of the anodic process on covellite have been obtained by galvanostatic method. It was established that the essential difference exists between the reaction mechanism in sulfate and chloride solutions. Also, the difference is exhibited in the nature of reaction product directly connected with the passivation of the electrode surface. Chronopotentiometric investigations have been performed in sulfate, nitrate, chloride perchlorate and mixed sulfate/chloride solutions applying different current densities. The shape of obtained curves indicate if there was a surface passivation and how intensive it was."

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