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By John Nell, Paul den Hoed

Carbochlorination tests were conducted with matched particle-size fractions of rutile, ilmenite and high-titania slag in a small bubbling fluidized-bed reactor. The effects of temperature, the type and proportion of solid reductant in the charge, and the fraction of Cl2 in the fluidizing gas were investigated. Tests confirm the need for solid carbon in the bed if chlorination is to run at high rates. With solid carbon in the bed, CO supplied with the fluidizing gas does not increase significantly the degree of chlorination after 75 minutes. Ilmenite is chlorinated more quickly than titania slag, which in turn is chlorinated more quickly than rutile. Rates of chlorination at 1100°C and 1000°C are much the same and significantly higher than at 900°C. Chlorination is associated with significant increases in particle porosity (even for rutile), which is brought about by the rapid initial chlorination of FeO and MnO (in ilmenite and slag) and (it is argued) by the chlorination of Ti2O3 which forms at high-energy surface sites. A reaction mechanism is presented; where possible, its validity is demonstrated by the support of empirical observations.

Jan 1, 2003

By Jia Ma, Lu-De Qiang, Zhi-Chao Liu, Chun-Feng Li, Guang Li, Bao-Bin Tang

"At present, research on the surface chemical properties of uranium minerals is very scanty, which restricts the research progress of uranium ore flotation process research. The research aimed at exploring the surface characteristics of two common uranium minerals and providing basis for flotation process to enrich uranium minerals in ore. This paper selected pitchblende and uraninite as the object of study, which are widely distributed in uranium deposits. We chose out the pure minerals of pitchblende and uraninite from different ores collected from different uranium deposits. By means of Zeta potential test and X-ray photoelectron spectroscopy (XPS) test, a preliminary study on surface characteristics of the pure minerals of pitchblende and uraninite was conducted. And the significance of the change of Zeta potential, the elements composition and valence state on the minerals surface for flotation was discussed. The research shows that, the Zeta potentials of pitchblende and uraninite in pure water are negative mainly when the pH value varies from 2 to 11, which maybe a result of the difference of ionization capacity between two kinds of oxy-compounds on the surface of minerals. On the surface of pitchblende and uraninite, the metal elements are mainly U, Th and Pb. U is mainly in the form of UO2, Th is mainly in the form of ThO2, and Pb is mainly in the form of Pb and PbO. Based on the surface characteristics of pitchblende and uraninite, we can select process and reagents appropriately in uranium ore flotation.INTRODUCTION Globally, the major challenges associated with exploitation of low grade ores are about finding economically feasible processes for reducing the mass of gangue minerals (Filippov et al., 2012). Among the beneficiation technologies of low grade uranium ores with complex minerals assemblage, flotation is the common process which is used to reduce production cost and eliminate the acid-consuming minerals (Li et al., 2016; Liu et al., 2015)."

Jan 1, 2018

By J. D. Miller

The more efficient production and use of mineral resources is a major objective of our sustainability efforts. Resource characterization is a critical component for optimization of the mine-to-mill process, including innovative processing for sustainable growth. Such characterization is now referred to as geometallurgy, with advanced instrumentation including, for example, particle size analysis, XRF, XRD, NIR, automated SEM/EDAX analysis (QEMSCAN, MLA), and high resolution X-ray micro tomography. Geometallurgical information is important for exploration, deposit evaluation; mine planning, design and analysis of separation processes, etc. Characterization of mineral processing particles in 3D is now possible using high resolution X-ray micro tomography (HRXMT), and such HRXMT systems have been installed at several laboratories around the world. After review of principles, the features of such HRXMT analyses are presented including size/shape, damage state, mineral phase identification, and evaluation/isolation of trace mineral particles. With new algorithms for image analysis, quantitative data treatment is possible for construction of liberation-limited grade/recovery curves, for the determination of specific crack surface area, and for complex texture analysis including grain exposure. Finally, new tomographic characterization possibilities are discussed to provide the foundation for the development of advanced, innovative processing strategies for sustainable growth. Keywords: X-ray tomography, resource characterization, HRXMT, particle size analysis XXVI INTERNATIONAL

Sep 1, 2012

By V. E. Vigdergauz

Possibilities of the analysis of potential energy of bubble-particle interaction on the basis of extended DLVO theory are discussed. Interaction energies of mineral silica, coal and pyrite particles with contact angles from 20 to 100 degrees and air bubbles in neutral and alkaline solutions are analyzed. It is shown that for hydrophilic silica, the formation of particle-bubble complexes (either in the area of primary or secondary potential minima) is impossible due to the high potential barriers (from 6000 to 140000 kT)and low values of the attraction force. There is shown that for coal and pyrite particles the energy of interaction vs. particle-bubble distance strongly depends on pH value. Improvement of floatability of minerals by the hydrophobization of their surface by collectors leads to the eliminating of potential barriers and the formation of the stable complexes of minerals and air bubbles in the area of primary potential minimum. In addition, due to hydrophobization of coal and pyrite changing pH has practically no influence on the energy of interaction. There are discussed results of the numerical calculations of normalized interaction forces in particle-bubble systems on the nanometer distances for pyrite, sphalerite, and chalcopyrite at contact angles up to 85° in comparison with the experimental data. The values of adhesion force for hydrophobized particles of coal and pyrite to air bubbles are about 10-5 N, that indicates stability of the formed flotation complexes. Examples of using the long-range and high-energy effect of hydrophobic interactions for improving minerals floatability are discussed. There are illustrated minerals wettability changes induced by the adsorption of thiol collector and hydrophobic polymer. Possibilities of flocculation and flotation of mineral slimes due the polymer-collector hydrophobic interactions are shown. Keywords: bubble-particle interaction, contact angle, extended DLVO theory, floatability

Sep 1, 2012

By Carlos Pereira, Fábio de São José, Francielle Nogueira

Votorantim Metals Corporation is one of the leader companies in the extraction of zinc in Brazil. One of its mines, located in the city of Vazante - MG, was composed by zinc silicate ores, but recent studies have indicated a change in mineralization type with arise of zinc sulphide’s ore bodies with disseminations of galena (PbS) and silver. The liberation size between sphalerite and galena in this ore occurs in very fine granulometry (approximately 18µm), fact that has negatively influenced into the flotation process. Aiming to reduce this problem, studies about the use of dispersing in the flotation process have started. Thus, this study investigated the action of different reagents dispersing on the stability of the suspensions. The tests were carried out with samples of mineral galena and sphalerite using four types of dispersing within two different dosages and two pH. The reagents tested were sodium hexametaphosphate, sodium silicate, carboxymethiylcellulose, and sodium polyacrylate. The results of the dispersion tests were analysed in relation to dispersion index. The tests with hexametaphosphate showed high dispersion for both galena and sphalerite. The sodium polyacrylate and arboxymethiylcellulose showed a high dispersion index for galena and a low index for sphalerite implying that reagent can be used in the concentration process of galena.

Jan 1, 2014

By P. Condori

In spite of the importance of the slurry transport and discharge in autogenous and semiautogen-ous (AG/SAG) mills, it is evident that a more comprehensive and useful model is still required. Semi-empirical models used up to now have many limitations and cannot be used beyond the ranges in which they were developed. The breakage of particles as they are transported along a mill com-plicates the experimental analysis and the modelling of the transport process within the mill. The interaction of the grate discharge and the pulp lifters, with the added issue of backflow from the pulp chamber into the mill, makes the discharge modelling process difficult. In order to overcome these difficulties, a mechanistic approach has been applied. The general transport and discharge model was subdivided into four independent models: Flow through the charge, flow through the grate, flow in the pulp lifter, and flow-back. This paper gives an overall description of the modelling approach and discusses in particular the modelling of transport of fluids through the charge. In order to evaluate and calibrate the model, experimental work was carried out. To evaluate the gradient pressure under different conditions of charge packing and flow rate, a specialised experimental rig with a highly sensitive pressure gauge was used. Preliminary results identify the differences of the charge and grate on the restriction of flow. The existence of a dynamic voidage in our particular system was more evident and as a result, a semi-empirical correlation for the voidage was developed. In general, results show that the me-chanistic model derived from Ergun?s equation for flow through a packed bed can be satisfactorily adapted.

Jan 1, 2014

By Svetlana Krashenina, Nebojsa Petrovic, Oscar Lopez

"As easily mined gold deposits are becoming increasingly rare, gold producers are turning to the processing of ores with polymetallic and copper mineralization. These base metals can create metallurgical and waste handling/disposal challenges, which can render the project uneconomic. Base metals such as copper compete for the cyanide reagent used to extract gold, necessitating the need to increase cyanide volumes and consequently, cyanide consumption costs. Copper will also stabilize in tailings water as weak acid dissociable cyanide, a form that is both difficult and costly to destruct. SART (sulphidization-acidification-recycling-thickening) process technology can be applied to remove base metal interferences in gold projects. SART breaks the copper-cyanide complex and precipitates the copper as a saleable copper sulphide concentrate. With the copper removed, the cyanide can be regenerated as free cyanide for recycle to the gold recovery process. This improves cyanide utilization efficiency and mitigates copper presence in tailings. Additionally, copper recovery generates an incremental revenue source to further improve project economics. Engineering Dobersek GmbH together with BioteQ developed a SART and AVR testing program to recover cyanide and maximize operational efficiencies at a gold processing plant in Kazakhstan with high cyanide consumption in the leach circuit. Results from on-site testing demonstrated that up to 99.98% of copper can be removed and precipitated as copper sulphide and 60-90% of cyanide can be recovered from the AVR and recycled for leaching, reducing total overall cyanide use. This paper provides an overview of the testing methodology and results together with a discussion on the potential of SART to improve gold production operations to deliver both environmental and economic benefits."

Jan 1, 2014

By B. McFadzean, J. Taguta

The enthalpy of immersion is the heat change arising from the replacement of the solid-gas interface with the solid-liquid interface when a solid surface is immersed in a liquid. Although immersion calorimetry has been established as a valuable and reliable means of determining solid surface properties such as wettability, it has seldom been applied in mineral processing research. In this study, precision solution calorimetry was employed to measure the enthalpies of immersion of different minerals in water. The enthalpies of immersion were then related to the first-order flotation rate constant as determined by the microflotation technique. The same measurements were also made on sulphide minerals whose surfaces were modified to different degrees of hydrophobicity using different percentage coverages of amyl xanthate collector. The enthalpy of immersion technique was capable of distinguishing and ranking minerals according to their wettability. All mineral types and collector-treated minerals conformed to the same relationship that was found between the enthalpy of immersion and the flotation rate constant. This conformed, empirically, to a power law equation. As the enthalpy of immersion decreased, there were large increases in flotation response for very small changes in hydrophobicity. In addition, a critical enthalpy of immersion (CEI) was found, above which no flotation could occur. The scatter in the data points could be corrected for by adjusting the rate constant using the density of the minerals to produce a robust relationship between the rate constant and enthalpy of immersion. These results have shown that the enthalpy of immersion is able to indicate both the natural mineral hydrophobicity and the extent to which collectors can render a mineral hydrophobic. This technique has considerable potential to be used as a sensitive and accurate measure of mineral surface wettability in order to predict flotation performance.

Jan 1, 2018

By N. D. Dementieva

Based on lab and pilot-plant tests to recover gold, silver and lead of a Russian deposit, a collective and flotation concentration flow sheet with lead and sulfide concentrates was proposed. The type of the deposit is gold-sulfide-quartz-bearing. The recovery of gold, silver, and lead to a lead concentrate was 47.4%, 68.1% and 70.7%, respectively. The grade of gold and silver grade was 170 g/t and 372 g/t, respectively. The mass percent of lead, zinc and arsenic mass percent was 41.7%, 0.34% and 0.63%, respectively. The recovery of gold and silver recovery to a sulfide concentrate was 50.1% and 28.8% at the grade of gold 20.5 g/t and silver 66.2 g/t. Sulfide concentrate with arsenic mass percent ~3% was biooxidised followed by CIL and obtaining metal at the site as well as zinc concentrate from bioleaching solutions with zinc mass percent 45% at its 64% recovery. The total gold and silver recovery using a developed technology with the account of their treatment at a polymetallic plant was 92.2% and 93.7%, respectively.

Sep 1, 2012

By T. Wajima

We tried to convert paper sludge ash (PSA) into zeolitic product with high cation exchange capacity (CEC) through acid leaching. Typically, PSA from incineration of paper sludge contains a high percentage of calcium in the form of anorthite (CaAl2Si2O8) and gehlenite (Ca2Al2SiO7). It is difficult to convert the ash with a high Ca content into zeolites, or at least into more desirable zeolite phases. Acid leaching with HCl was applied to reduce the Ca content to synthesize zeolitic product with high CEC. The raw ash was treated with 1 M, 3 M, and 5 M HCl solution for 0.5~24 hours (the ratio of the ash to volume of HCl solution was 1/4), and then zeolitic product was synthesized from leached ash through the reaction with 2.5 M NaOH solution at 80 oC for 24 hours. During acid leaching, gehlenite is readily dissolved in a lower HCl concentration solution than anorthite. With increasing HCl concentration, the amounts of Ca, Mg, Si, Al, Fe and Ti extracted from the ash increased. Ca and Mg contents were easily extracted from ash than other elements. The contents of Ca and Mg extracted rapidly at initial stage, and then levelled off. The saturation times of Mg and Ca are almost 0.5 h using all concentrations of HCl solutions. After the synthesis from leached ashes, zeolite-A and -P were synthesized from ash leached in 1 M HCl solution, and 3 M and 5 M HCl solutions, respectively, regardless of leaching time. With in-creasing HCl concentration, the Ca content eluted from the product decreased, due to the removal of Ca via acid leaching before the synthesis, while the Na content eluted from the product increased to 3 M HCl and then decreased, which was almost similar to the CEC of the product, due to the ion exchange of Na-type zeolitic phase in the product. The change of zeolite phases in the product and the CEC of the product depend on the concentrations of Si and Al in the solution during the synthesis. The highest CEC of the product is about 220 cmol/ kg, which was synthesized from the ash leached in 3 M HCl solution.

Jan 1, 2014

By Gabriela Pino, Maurício Torem, Diego Veneu

Because of its simplicity, economy and biocompatibility, research regarding the use of microorganism for decontaminating heavy metals produced by many industries is an area of growing interest. Also, there is a stringent need for the control of toxic metals produced during various production processes and released into the aqueous environment in order to avoid damage relevant to soil or groundwater contamination. Among the available treatment technologies, sorptive flotation has been considered as a promising alternative for the wastewater treatment. In the present study Streptomyces lunalinharesii strain was applied as bioreagent for the removal of copper, cadmium and zinc. The removal of those metal ions depends mainly on the respective pH value, influencing the aquatic speciation during the process, as well as the zeta potential of the system and biomass concentration. Langmuir and Freundlich isotherms have been depicted. Dispersed air flotation was applied as the subsequent separation method for harvesting the suspended metal laden microorganisms, following the biosorption of copper, zinc and cadmium. The investigated parameters (in batch mode, laboratory scale) were in this case the saturator pressure, the coagulant concentration and the recycled flow. Applying the optimum defined conditions, over 60% removal of metal ions have been achieved in one stage and simultaneously, quantitative separation of the used (metal-loaded) biomass has been obtained.

Jan 1, 2014

By Alejandro Rubio-Lopetegui, Gonzalo Montes-Atenas

The occurrence of Enargite (Cu3AsS4) in hydrometallurgical plants bears a number of challenges. One question lies on how Copper and Arsenic can be selectively extracted from the solid surface structure when immersed in aqueous solution. The leaching of Enargite in ambient conditions has been extensively studied; nevertheless, challenges regarding the process kinetics and surface structures enabling the extraction process remain ill-understood. Prior knowledge indicates that different conditions of pH, Eh, temperature, speciation of the aqueous phase or variations of these parameters defines the overall rate at which metals and other elements will be transferred to the solution. One aspect that the research studies have seldom addressed involves studying the main features of the surface structures formed during the leaching process at the outmost surface atomic layer. Such structures will mediate between the solid bulk and the solution to undertake subsequent stages of leaching process. The aim of this research work is to critically analyze the state of the art of Enargite electrochemistry from the mediator formation-dissolution mechanisms standpoint occurring at the mineral-solution interface. The most probable mediator species reported in the literature were found to be: Arsenolite and Sulfur (acidic media), Covellite (acidic and alkaline media) and Tenorite (alkaline media). As a result of this analysis, it was observed that the surface speciation was not in full agreement with the previous knowledge suggested to explain Enargite leaching reactions and, therefore, modified Eh-pH diagrams are presented. The acquired insights on the surface structures rising from the Enargite-aqueous solution interactions is further revised to provide new experimental protocols towards selectively separating Copper and Arsenic through hydrometallurgical paths.

Jan 1, 2014

By S. Groudev

Acid drainage waters generated in the uranium deposit Curilo, Bulgaria, were treated by means of a pilot-scale passive system consisting of a permeable reactive multibarrier and a constructed wetland connected in a series. The multibarrier had a total volume of 23 m3 and consisted of an alkalizing limestone drain and an anoxic section for microbial dissimilatory sulphate reduction, bio-sorption and additional chemical neutralization. The waters had a pH in the range of about 2.5 ~ 4.0 and contained radionuclides (uranium, radium), heavy metals (copper, zinc, cadmium, lead, nickel, cobalt, iron, manganese), arsenic and sulphates in concentrations usually much higher than the relevant permissible levels for waters intended for use in agriculture and/or industry. The water flow rate through the multibarrier varied in the range of about 1 ~ 17 m3/24 h, reflecting water residence times of about 300 ~ 18 hours. An efficient removal of pollutants was achieved by the multibarrier during different climatic seasons, even during cold winter days at external air and water temperatures close to 0oC. The multibarrier effluents were enriched in dissolved organic compounds and in some cases still contained manganese and iron in concentrations higher than the relevant permissible levels. These pollutants were removed in the constructed wetland as a result of the activity of different heterotrophic microorganisms, including some bacteria able to oxidize the bivalent manganese and iron ions to Mn4+ and Fe3+, respectively.

Jan 1, 2014

By John Ralston

"Interfacial chemistry plays a pivotal role in bubble-particle capture, for it controls whether or not attachment occurs. Surface heterogeneity, degree of surface hydrophobicity, bubble nucleation and related phenomena influence the stability of the aqueous wetting film between a particle and an approaching bubble. The latter must be unstable if capture is to occur. Various techniques that may be used to quantify this interfacial, chemistry-dominated behaviour, are described.The efficient capture of specific particles by rising bubbles and the delicate control of interfacial chemistry that leads to selective capture are central issues in froth flotation. For efficient capture to occur between a particle and a bubble, they must undergo a close encounter, a collision process dominated by hydrodynamics. Should this encounter bring the particle and bubble within the range of attractive forces, the intervening liquid film between the bubble and the particle will drain, leading to a critical thickness at which rupture occurs. The liquid-vapour interface then retreats over the solid particle surface until a stable wetting perimeter is established. The particle and bubble are then joined after this attachment process. The particle may only be dislodged from this state if it is supplied with sufficient kinetic energy to exceed the detachment energy in this detachment process. These various events are now well documented and may be followed using high-speed videomicroscopy (Schulze, 1984; Nguyen et al., 2001).The process of collision can now be described quantitatively for single bubbles colliding with bubbles under various flow regimes (Dai et al., 1998) and appropriate scale up is possible for multiple bubble particle collisions occurring under turbulent conditions (Pyke et al., 2002). In this paper we will be concerned with the role of interfacial chemistry and how this influences the attachment process."

Jan 1, 2003

By N. R. Mandre

In the present work an attempt has been made to study beneficiation of low-grade iron ore associated with manganese clay by selective flocculation. The representative samples obtained for this purpose were initially subjected to chemical and mineralogical studies. The chemical analyses indicated 42.56 % Fe, 6.25% Mn, 8.72 % SiO2 and 13.60 % Al2O3 in the representative sample. The mineralogical analyses carried out under optical microscope showed that the ore mineral predominantly comprised of iron oxides and hydroxides along with manganese and silicate as gangue minerals. Prior to the beneficiation studies, the samples were subjected to settling tests. These tests were carried out by using poly acrylic acid (paa), poly acryl amide (pam) and guar gum (gg) as the flocculants. From these studies it was observed that settling rate of particles increases with increase in pH and a maximum settling rate of 0.23 cm/secwas obtained at pH 9 in presence of poly acryl amide. Further, the samples were subjected to selective flocculation studies using above-mentioned reagents. From these studies better results were obtained in the experiments carried out with poly acryl amide as the flocculant. Thus, it was possible to upgrade the iron content from 42.5 to 53%, with a recovery of 92%. However, 51% Fe with recovery of 87% and 50% Fe with recovery of 94 % was obtained using poly acrylic acid and guar gum respectively.

Sep 1, 2012

By T. Ueda, T. Oki, S. Koyanaka

"Accurate assessment of the liberation state of crushed ore particles is important for efficient mineral processing. In general, the liberation state is assessed by two-dimensional (2D) measurement of polished ore sample sections. However, this 2D measurement inevitably suffers from overestimation of the degree of liberation, known as stereological bias. This arises from the fact that biphase particle sections of which only one phase happens to have been cut are indistinguishable from liberated particles. To date, several stereological correction methods have been proposed, but their applicability for various types of particles has not yet been sufficiently examined, and this tends to undermine their practicality. We have addressed this problem using a numerical-analytical approach in which various types of biphase particles are modeled, and the 2D sectional information is compared with actual three-dimensional (3D) information. Through simulations, we revealed a general relationship between the internal mineral structure of particles and the stereological bias. Finally, we have developed a unique stereological correction method in which the texture (a 2D pattern characteristic) of particle sections is used to estimate the internal structure of particles, and thereby the stereological bias. KEYWORDS Mineral liberation, stereological bias, texture analysis INTRODUCTION Mineral liberation assessment of 2D particle sections inevitably suffers from stereological bias; that is, overestimation of the degree of liberation. Stereological bias is caused by the fact that a composite particle can be misidentified as a liberated particle when only one phase happens to have been cut in sectional measurement. Stereological bias has attracted attention since Gaudin pointed out its importance in 1939 (Gaudin, 1939). Several attempts have been made to measure the 3D liberation state directly, avoiding the bias, using X-ray computed tomography (Gay and Morrison, 2006; Lin and Miller, 1996; Miller et al., 2003; Miller et al., 2009; Reyes et al., 2017; Videla et al., 2007). These have provided useful information through laboratory testing, but further technical refinement is necessary for practical usage, to overcome the technique’s limitations in terms of resolution, assessment of minerals of similar density, and speed. Therefore, for practical purposes, detailed information regarding mineral phase geometry is obtained by sectional analysis, using automated scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDX)-based analysis (e.g., with a mineral liberation analyzer (MLA) (Fandrich et al., 2007; Sandmann, 2015)); and the development of an effective method of stereological correction, which predicts the relevant bias and transforms the measurable 2D degree of liberation into its 3D counterpart, is an important research aim."

Jan 1, 2018

By Di Liu, Yongjun Peng

"It was identified that clay minerals adversely affect fine coal flotation through slime coatings. In the study, it was interesting to find that an anionic polymer dispersant, lignosulfonate, successfully mitigated the negative effect of clay minerals in coal flotation using fresh water, but in saline water, it exacerbated coal flotation.In order to understand the mechanisms underpinning the different behaviour of lignosulfonate in coal flotation using fresh and saline water, the adsorption isotherm, and dynamic light scattering (DLS) measurements were conducted in this study. While DLS monitored the molecular conformation change (swelling or shrinking) of the polymer in fresh and saline water, adsorption isotherms enabled polymer adsorbed amount on clay and coal mineral surfaces to be determined. It was found that lignosulfonate adsorbed on the coal and clay mineral surfaces providing effective electrostatic repulsions and resulting in a mitigation of clay minerals from coal surfaces in deionised water. In the presence of saline water, however, polymer molecular conformation changed. Polymer molecules were compressed and adsorbed in form of aggregates. The adsorption amount of lignosulfonate on clay minerals increased in saline water. A low dosage of lignosulfonate could not provide sufficient electrosteric repulsion to disperse clay minerals. Moreover, the high adsorption amount of the polymer on coal and clay surfaces led to a more hydrophilic coal surface, and coal flotation was therefore depressed in saline water. This study provides a new insight into understanding the role of anionic polymeric dispersants in mineral flotation using different quality water."

Jan 1, 2014

By G. Weingrill, H. Flachberger, J. Neubacher

The so called Bublon®-process is an innovative process for the controlled expansion of volcanic glasses such as Perlite and for thermal treatment of other minerals. In this manner, functional light fillers with astonishingly altered physical properties can be manufactured. In contrast to conventional Perlite expanding processes no fossil fuels are burned in order to achieve the expansion. Instead, the feed material is heated electrically mainly by radiation based on heat transfer from heating elements. The main advantage is the better controllability of the production process. Therefore, the heating elements are segmented along the flow of the particles, hence in direction of the ongoing expansion. Overheating of the particles, which ultimately leads to the destruction of the particle surfaces and consequently decreasing the quality of the expansion product, can be reduced significantly. Due to flow characteristics and settling behaviors of fines the lower particle size limit of the feed in this process is restricted to not less than 100 µm. Otherwise process instabilities are to be expected. Manufacturing industry demands light and fine hollow microspheres. Therefore, a proven cooperation between Montanuniversität Leoben and Bublon GmbH was formed to develop a new process called ‘Bublite’. This issue was addressed by changing the conveying principle into a pneumatically conveying system transporting particles from the bottom to the top of the kiln by the means of a drag flow. This approach makes it possible to handle the difficult flow patterns in the kiln and to control the retention time of the particles in the heat transfer zone. As a result, it is now possible to expand very fine Perlite particles into a high quality functional lightweight filler with a glazed-closed surface. The dependence of the polymer industry on importing this kind of fillers from overseas can be reduced by producing it close to sites of demand. Also the Perlite mining and processing companies benefit from this technology because the mine lifespan and the output of the processing plant can be increased.

Jan 1, 2018

By Rogerio C. Guimarães, Antonio E. C. Peres

The production of phosphate concentrates (phosphate rock) from slimes represents a challenge to the phosphate industry worldwide. In Brazil, this challenge is particularly relevant due to the consistently low P2O5 grades and the igneous origin. The first industrial experiences of producing phosphate rock from slimes (-44µm or -325#) fraction started at Arafertil, currently Bunge Fertilizantes SA, in Araxá, in the 1980.s. This production corresponds, nowadays, to 35% of the total production of concentrates in the company (830,000t/year) in a circuit consisting of desliming in 40mm microcyclones and concentration in flotation columns, corn starch and fatty acids being utilised as reagents. The performance of slimes flotation and the process control, at Bunge´s concentrator, were improved after the introduction of column flotation technology, in the first half of the nineties. The column flotation technology for slimes recovery was expanded to other Brazilian concentrators still in the nineties: Ultrafértil (Catalão - GO), Bunge (Cajati - SP), Fosfértil (Tapira - MG) and Copebrás (Catalão - GO). At present the Brazilian production of phosphate rock is approximately 4.5Mt/year, with a strong trend for a market increase. Genuinely Brazilian technology is utilised for the processing of slimes, the concentrates representing 11 to 13% of the overall production. The production of apatite concentrates from slimes was relevant to increase phosphate recovery and reduce costs, contributing to the growth of the fertilisers industry.

Jan 1, 2003

By Olli Haavisto, Heikki Häkkänen, Tommi Kauppinen, Navid Khajehzadeh

Raman analysis is a well-established method for finding the abundant minerals in an ore sample. In this study, Raman spectroscopy is tested as a method for rapid and contactless on-line mineral analysis. Rapidness might enable on-site analysis of rock drillcore, which in turn would lead to more cost-efficient solutions in mineral exploration. This paper discusses the use of Raman analysis to identify minerals and to measure their concentration. The sample set under study consists of rock drillcore collected from Agnico-Eagle Kittilä Mine, Finland. Selected parts of the sample set are measured by Raman spectroscopy and the minerals are identified using reference spectra from a public source. Moreover, the direct measurement of concentration of different minerals with the help of Non-negative least squares (NNLS) optimisation algorithm is considered. The optimisation algorithm was constructed to form a linear combination of reference spectra which best represent the measured spectrum, or an average of measured spectra, from an ore sample. The results show that NNLS can identify abundant minerals in a given sample. Also through this method of analysis the results of a traditional point-count method can be expanded: It was observed that, due to grain size, multiple minerals consistently appear in the spectra measured over an area, which means that point-count method is not a proper way to interpret the spectra. This can be seen as a new result, as formerly the discussion has attended to other methods.

Jan 1, 2014