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By H. R. Manouchehri

Large variations in flotation characteristics of minerals have been observed in winter and summer in plant practices as a result of changes in pulp temperature. Variations in temperature may affect the quality for pulp and related process water through changes in dissociation of different chemical species within the pulp, as well as changing in gas and metal hydroxide solubility, reagent adsorption and its stability on mineral surfaces, water/pulp viscosity, etc. All of these affect the flotation characteristics of specific mineral to some degree or another. It has been observed in Cu-Pb-Zn and/or Pb-Zn sulfides flotation that sphalerite (ZnS) flotation is strongly affected by changes in pulp temperature. Plant practices have shown that at the both low, e.g., T <10-12°C, and high, e.g., T > 60°C, the recovery for copper activated sphalerite is dramatically dropped. Within this paper the effect of pulp temperature on flotation characteristics of sphalerite is brought into considerations and laboratory flotation tests were conducted in conjunction with surface and solution chemistry analysis to understand the effect of temperature on sphalerite recovery. The effect of temperature seems to be complex since the temperature affects both the physical (hydrodynamics) and chemical phenomena in the flotation cell. In fact all sub-processes in flotation, i.e., collision, attachment and detachment, are affected by changing in temperature. Experimental results indicating that at alkaline pH values, e.g., 8.5 to 10.5, the recovery for copper-activated sphalerite is dramatically reduced when temperature is below 10-12°C, which is in agreement with plant practice at Boliden?s Garpenberg plant in Sweden. However, results from other studies indicated that the zinc recovery is also considerably decreased at high pulp temperatures, i.e., 62°C and above.

Sep 1, 2012

By David Dreisinger

"The leaching of base and precious metal ores and concentrates continues to progress in both laboratory study and industrial application. These developments are being driven by the need to respond to difficult ores and concentrates that are not amenable to conventional treatment. In many cases alternatives are being developed to conventional treatment (e.g. Pyrometallurgy) for technical and economic reasons.In this paper, a brief general review of some new developments in leaching will be followed by a more detailed explanation of three process developments that have either been industrially applied or are expected to be applied in a short time frame. The three processes to be reviewed in detail are the Mt. Gordon Copper Process, the Anglo American Corporation/University of British Columbia Copper Process and the PLATSOL Process. These leaching processes operate at low (90°C), medium (150°C) and high (220°C) temperature and are successful in quickly and completely extracting metal values from ores and concentrates.INTRODUCTIONThe process of leaching is widely used in hydrometallurgy to selectively recover a metal of interest from an ore or a concentrate. Leaching and by extension hydrometallurgy is well established in the recovery of copper (copper heap leach ? SX-EW), nickel (Moa Bay and Caron process), zinc (roast ? leach ? electrowin and zinc pressure leach), gold (cyanidation) and uranium (acid sulfate leach). Of course this success extends to many of the metals found in nature. Recently, the importance of hydrometallurgy appears to be increasing with hydrometallurgy viewed as an attractive alternative to both traditional mineral processing and conventional smelting/converting/refining. This increasing interest has led to intensive study and increasing application. Selected developments include:Copper ? the Mt. Gordon process and new concentrate processes such as INTEC, Activox, CESL, Dynatec, Total Pressure Oxidation, MIM Albion, BioCop, and the AAC/UBC Process.Nickel ? Voisey Bay process for hydrometallurgical treatment of Voisey Bay concentrate, HPAL processing of laterites at Murrin Murrin, Bulong and Cawse, atmospheric leaching of laterites, heap bioleaching of nickel sulfides by Titan Resources (Australia).Zinc ? establishment of zinc leach, solvent extraction and electrowinning technology for treatment of the Skorpion deposit in Namibia, new developments in atmospheric and pressure leaching, the Hydrozinc process.Gold ? development of a number of thiosulfate leaching processes for recovery of gold from refractory carbonaceous ores or concentrates."

Jan 1, 2003

By M. M. Bugarin, P. J. van Staden, V. T. Conic, S. S. Dragulovic, R. M. Kovacevic, D. B. Milanovic

"The mineralogical and physico-chemical characteristics of a polymetallic sample from a mine of West Serbia suggest that it can be classified as a SEDEX type of ore. Those ores contain multiple value components, being inter-dispersed as fine grained aggregates. This prevents concentration by gravity or flotation concentration processes. Mineralogically, the valuable metals (Cu;Zn;Pb;Au and Ag) occur as pyrite, sphalerite, galena, tetrahedrite, chalcopyrite, covellite, arsenopyrite, and non-metallic minerals (barite, and waste minerals). Novel technologies are under development within this project for the recovery of all valuable metals from this very complex material. The work comprises the further treatment of solid residue obtained after Cu and Zn extraction by bioleaching, for the subsequent recovery of Pb and the precious metals Ag and Au. The residue is first treated with a saturated sodium chloride solution, whereupon a chloride solution of lead (NaPbCl3) is obtained. From the chloride solution, lead was deposited in the form of lead carbonate, followed by reductive melting, whereupon lead anode was obtained. Electrolytic refining of the lead anode, using a solution of PbCO3 in methane sulphonic acid (MSA-Methanesulfonic acid, min 99.5% CH4O3S, density 1.48 kg/dm3, Manufacturer: Carl Roth) as an electrolyte, yielded refined lead cathode. It should be noted that, after precipitation and separation of lead carbonate, the sodium chloride solution is restored to its original composition by the addition of make-up reagents and returned for another lead-sulfate leaching cycle. The solid residue obtained after leaching lead-sulphate, is leached in thiosulphate solution, with the addition of an activator, a catalyst and lixiviant for gold, to yield a thiosulphate solution of gold and silver. Since the content of gold and silver in solution is low (below 1 mg/dm3), they are first electrolytically concentrated on steel cathode and then refined to pure metals using well-known chemical methods. Note that, after the electrolytic separation of gold and silver, thiosulphate solution is recycled to the leaching step."

Jan 1, 2018

By H. Sarvamangala

Selective separation of alumina, silica, calcite and apatite from hematite was achieved through microbiologically induced flotation and flocculation in presence of bacteria (B.subtilis) and that of hematite from apatite after interaction with yeast (Saccharomyces cerevisiae). Bacterial and yeast metabolites containing extracellular proteins were characterized from mineral-grown cell free extract. Bacteria and yeast can adhere to mineral surfaces and influence subsequent separation of the minerals. Bacteria functioned as a stronger depressant for hematite, while yeast cells depressed apatite at neutral pH. Selective affinity of the bacterial and yeast cells towards the mineral surface was observed through adsorption studies. Extracellular proteins (EP) were isolated from B.subtilis and yeast. The protein profile of the EP of bacterial and yeast cells grown in presence and absence of minerals was studied. This study has demonstrated the utility and amenability of microbially-induced mineral beneficiation of iron ores through bacterial and yeast cells and their metabolic by products.

Sep 1, 2012

By Walter W. Focke, Zola Kwela, Willem van der Merwe, Arao Manhique

"The advantages of the de Wet zirconium process for the manufacture of AZST from zircon sand include: Fewer processing steps; removal of radioactivity by leaching rather than by precipitation; alkali reagent recovery in the form of a sodium silicate solution that is essentially free of radioactivity; fewer waste streams and less waste to discard.Here we report on our efforts at maximizing the alkali recovery in the sodium silicate product stream: Milled zircon, d50 ˜ 9 µm, was fused with caustic soda pearls in open reaction vessels at temperatures between 650°C and 850°C. Fusion times of 1, 2, 4, 24 and 336 hours (with intermittent milling) were investigated.For prolonged fusion times the fusion products approached equilibrium compositions. However, the phases Na2ZrSiO5 and Na4Zr2Si3O12 observed at 850°C did not form at 650°C. Since they do not hydrolyse in water they limit the recovery of alkali. For 2-hour fusions a broad spectrum of non-equilibrium reaction-products, that are rich in sodium silicates, is formed. Optimum process conditions, with respect to NaOH recovery, correspond to a 2:1 stoichiometry and fusing for 2-hour at 850°C. At these conditions the alkali recovery is ca. 78% and the zirconia yield is ca. 57%."

Jan 1, 2003

By Ali Dehghani Ahmadabadi

Gravity separation technique is widely used in mineral beneficiation practices for its low cost, ease of operation, and eco-friendly nature. The most commonly used gravity methods for beneficiation of iron ores are shaking table, jig and spiral methods which aren&apos;t very effective for iron mineral fines. Multi-Gravity Separator (MGS) is suitable for the treatment of fines with a maximum particle size of approximately 500 µm. This study was performed on a low-grade haematite iron ore from Chadormalutailing dams. Detailed mineralogical, physical and chemical characteristics of a goethiticlateritic iron ore showed that the sample contained porous and friable oxides and hydroxides of iron. The ore sample had a feed grade of 35% Fe, 1.1% FeO, 15.5% SiO2 and 8.5% Al2O3. Haematite and goethite are the main iron-bearing minerals while quartzite and kaolinite are the major gangue mineral constituents. In this paper, the statistical evaluation and optimization of grade and recovery using a factorial design of experiment (DOE) method has been carried out for Chadormalulow grade ultra-fine haematite tailings with MGS. The input process parameters considered are drum speed, tilt angle, wash water flow rate and pulp density. The results show considerable improvements in both the quality characteristics such as grade and recovery with statistical evaluation and optimization, compared to the initial value of grade and recovery. Keywords: multi-gravity separator, mgs, statistical evaluation, optimization, haematite

Sep 1, 2012

By Ricardo Montero

At this time, over 300 tons of Au are used in electronic equipment each year with other precious and strategic metals such as Ag, Pt, Pd, Cu, Nb, Ta, etc. After the use-phase, the electronic devices become electronic waste (e-waste); consequently it is important to consider e-waste as a secondary supply for recovery of these metals. One of the most important components is the printed circuit boards (PCBs) because the amount of their precious metals is ten times higher than rich precious metals bearing ore. This paper presents the recovery of Au, Ag, Cu and Nb from PCBs of discarded computers using leaching column technique. The amount of these metals in used PCBs was: 613 g/ton of Au, 1515 g/ton of Ag, 36 g/ton of Nb and 23.4 % of Cu. The PCBs were crushed with a hammer mill until reaching a particle size between 3.33 mm to 0.43 mm. Then, it was leached with sodium cyanide solution in a glass column using the following conditions: sodium cyanide concentration 4 g/L, flux 20 L/kg PCBs day, pH between 10.5 to 11 and leaching time 15 days. Every day, after leaching, the pregnant solutions passed through a column with activated carbon to complete the closed loop system. The following recoveries were obtained: 46.6% of Au, 51.3% of Ag, 47.2% of Nb and 62.3 % of Cu. The products obtained are: a) loaded carbon that contains the desired metals and b) processed PCBs with precious metal contents. A preliminary technical-economic study shows the feasibility to create a small-scale PCBs recycling plant. The initial investment is on the order of US$ 155 639, considering the recovered metals from loaded carbon. The internal rate of return for 10 years period (IRR) and net present value (NPV) estimated are 27% and US$ 105 926 respectively. Keywords: printed circuit boards, recovery, precious metals, niobium, leaching column

Sep 1, 2012

By Jan Svoboda, Toyohisa Fujita

"The current status and history of innovation in magnetic methods of material treatment are reviewed. The milestones and key drivers of innovation are identified, advantages of magnetic separation in comparison to other physical methods of material manipulation are discussed and reasons for failure to live up to its potential and expectations are identified. The future focus in such diverse areas as mineral processing, waste treatment, recycling and biosciences is discussed and the research and development needs are outlined.Our walk through the innovation landscape in magnetic separation illustrates the enormous effort that has been expended over the years to convert a wealth of novel idea into workable techniques. Remarkable progress has been achieved and numerous successful innovations have been introduced into material treatment operations. On the other hand these techniques have experienced their fair share of failures. The reasons for these cover a wide spectrum of risks that accompany any effort to implement new technology."

Jan 1, 2003

By Kunihiko Yamaguchi, Gjergj Dodbiba, Toyohisa Fujita

Usually magnetic separation is performed to separate ferromagnetic, paramagnetic and diamagnetic particles by controlling magnetic field strength. In this research the wet high gradient magnetic separation at various kinds of magnetization of medium has been investigated to separate different kinds of magnetization of paramagnetic mineral particles from each other. Most of week paramagnetic particles are captured at high magnetic field using superconducting magnet. If the magnetization of fluid is larger than that of paramagnetic particle, the paramagnetic particle cannot be captured in the direction of magnetic field. The paramagnetic particles of different magnetization such as hematite, chromium oxide, perovskite and rutile are separated in different magnetization of fluids. These particles are present in the incinerated bottom ash. The separation is useful to recover titanium oxide from bottom ash and the removal of chromium of bottom ash is important to reuse the bottom ash as cement. The used fluids are paramagnetic liquids dissolving paramagnetic salts and the water based magnetic fluid dispersing the stable ultrafine magnetite. The dispersion condition of particles related to zeta-potential of the suspension feed is also important to separate effectively by controlling pH

Jan 1, 2014

By S. J. Liu

The conventional collector for bauxite mineral is oleic acid, which is highly insoluble and must be used in high dosage in bauxite flotation operations, that is the great drawback of oleic acid in use. A series of hydroxamic acid were synthesized, and their collecting ability to certain minerals in bauxite: diaspore, kaolinite were studied. The collecting power of various reagents to diaspore in an incremental sequence were shown as follows: benzyl hydroxamic acid<amylic hydroxamic ac-id<heptylic hydroxamic acid<oleic acid<octylic hydroxamic acid; while the incremental sequence of the collecting power to kaolinite was like this: benzyl hydroxamic acid<amylic hydroxamic ac-id<heptylic hydroxamic acid<octylic hydroxamic acid<oleic acid. It could be seen that octylic hydroxamic acid had the capability of high collectivity and good selectivity, and octylic hydroxamic acid was chosen to use in the following experiments. Reduced zeta potential showed the adsorption of the anionic collector on the mineral. By the adsorptive capability and IR tests, the adsorption of octylic hydroxamic acid on diaspore was determined to be chemical absorption, which was greater than that of oleic acid, as it was physical absorption. Results of floatation experiments on manually mixed minerals indicated that the collectivity and selectivity of octylic hydroxamic acid were better than oleic acid.

Jan 1, 2014

By W. Z. Yin

It is investigated systemically in this paper that the granularity of the precursor, ZnC2O4?2H2O, is influenced by synthetic conditions. Instantaneously adding of precipitation agent is able to control the mean size of precursor ZnC2O4?2H2O under 300nm, which has great function to obtain well-dispersed ZnO nanoparticles in the next step, pyrolysis. The pyrolysis kinetics model of ZnC2O4?2H2O powder is obtained. Two steps take place during the pyrolysis. The first is dehydration, which the pyrolysis kinetic model is 2(1-a)2/3(chemical reaction), A=8.3×108s-1, E=(75.82±3.00) KJ/mol. The second is formation of ZnO, which the pyrolysis kinetic model is (1-a) (random nucleation and latter growth), A=8.45×1028s-1, E=(360.54±12.00)KJ/mol. ZnO nanoparticles obtained by pyrolysis take on self-growth behavior. It is resulted that for precursor ZnC2O4?2H2O pyrolysis time takes obvious influence on the partilces size under 420?, 500? and 600?. Finally, a new flow sheet for synthesis of ZnO nanoparticles is investigated, in which blendes is used as raw material and hydrometallurgy is introduced into it. The whole flow sheet has no industrial wastes, that is all byproducts can be used in the flow sheet recycled, resulted in the de-crease of productive cost and industrial wastes.

Jan 1, 2014

By Sanjay Agarwal

Polymetallic sea nodule is a good source of manganese having 22.3% Mn, 5.4% Fe, 6.14% Si, 1.1% Cu, 1.15% Ni, 0.076% Co & others. These nodules are available in plenty on the sea beds, generated over thousands of years. Nodules mainly consist of manganese dioxide and iron oxide phases and other metals are entrapped in the complex cage of these Mn-Fe oxides phases.World-wide research is going on sea nodules as an alternative future source of many metals, which has led to intensified efforts to develop practical and economical processes for recovery of these metals. Very little attempt has been made world over on manganese extraction from sea nodules. We at CSIR-NML, India have developed a direct reduction smelting process of nodules to recover manganese as Fe-Si-Mn alloy. This alloy is extensively used in the steel industry as deoxidizer and as an alloying element to make different grades of steel. Lab scale experiments were conducted to study the manganese distribution between Fe-Si-Mn alloy and FeO-SiO2-MnO-CaO-Al2O3-MgO slag at different temperatures by varying the basicity of the slag. The direct reduction smelting of nodules is carried out on 1 kg scale in 50 kVA electric arc furnaces to have Cu, Ni and Co alloy and Mn rich slag. This manganese rich slag is further treated in 50 kVA arc furnace to produce Fe-Si-Mn alloy. The composition of Fe-Si-Mn alloy obtained is in the range of Mn: 60-65%, Si: 14-17%, C: 1- 2%, S: 0.03% and the balance iron which is acceptable grade for industrial use. The equilibrium amount of MnO in the final slag is controlled by the temperature of the final melt and the silica, lime, alumina content of the final slag. Increasing the basicity of the slag plays a major role in minimizing the loss of MnO to slag, increasing the amount of SiO2 of the slag, increases the manganese loss in the slag. Increasing the CaO/ Al2O3 ratio of the slag decreases the manganese loss in the slag. Increasing the MgO/CaO ratio of the slag increases the manganese loss in the slag. Thus by adjusting

Sep 1, 2012

By Silvia Serranti, Giuseppe Bonifazi, Roberta Palmieri

The possibility to develop an efficient recovery and reuse of concrete materials from Demolition Waste (DW) represents one of the main targets applied to end-of-life constructions dismantling/recycling. The need to recycle end-of life concrete materials is strongly increasing in these last years for several reasons: i) the decrease of steady supplies of good quality natural aggregates, ii) the need to secure ample supplies of concrete aggregates to the construction industry and, finally, iii) the environmental constraints limiting the DW wastes disposal. The fulfilment of these goals produces several benefits, that is: i) a reduction of new resources consumption, ii) a strong reduction of the costs linked to transport and energy production, iii) the possibility to utilize materials, otherwise lost (e.g. land filled), iv) land preservation and, finally, v) the reduction of the environmental impact of new exploitation activities. A lot of efforts have been addressed to develop, set-up and apply innovative technologies to maximize DW conversion into useful secondary raw materials. The possibility to utilize efficient, reliable and low cost analytical tools to perform detection/control actions: i) to assess concrete characteristics, before demolition, and ii) to detect the presence of contaminants in coarse aggregates (e.g. bricks, gypsum, steel, glass, plastics, wood, etc.) represent the key issues to fulfil in order to develop innovative process/control actions/procedures inside the DW sector. In this paper a new technology, based on HyperSpectral Imaging (HSI) sensors is investigated to develop suitable and low cost strategies finalised to define and implement innovative smart detection engines for sorting and/or DW flow stream quality control, addressed to perform recovered materials and/or products certification. The proposed sensing architecture is fast, accurate, affordable and it can strongly contribute to bring down the economic threshold above which recycling is cost efficient.

Jan 1, 2014

By Bertil I. Pålsson

The most common REE containing mineral that is worked today is bastnäsite. It means that mineral processes are adapted to it and that the metallurgical separation techniques for winning of individual REE are adapted to bastnäsite concentrates. For all other deposit types, suitable mineral processing methods and separation technologies need to be adapted and/or developed. Preliminary mineralogical analyses indicate that slightly less than half of the REE in the tailings dumps at LKAB/Kiruna are associated to apatite. The rest is in the minerals monazite (maybe associated to apatite) and allanite. At least allanite is probably not floatable with reagents commonly used for apatite. Mass and element distributions for the tailings sand reveal that very little apatite is present above 300 µm, and that approx. 30 % is below 20 µm. REE does not follow P2O5 completely and are also present in coarser fractions. Flotation results show that the best condition for both apatite and REE winning is pH 9, high collector addition and low dosage of water glass. Under these conditions, the lab-scale flotation gives an apatite concentrate with at least 30 % P2O5 at 70 % recovery. REE follows apatite in the cleaner steps but only partly. Its recovery is approx. half compared with apatite. The reason for the low REE recovery is likely to be that REE to a large extent is trapped in non-winnable minerals, especially allanite. The REE grades in the concentrate are expected to be in the range 3000 ? 4500 g/ton. Keywords: flotation, REE, apatite, monazite, allanite

Sep 1, 2012

By Hideki Yamamoto, Norihiro Murayama, Junji Shibata

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

Jan 1, 2003

By K. Price, G. Wang, L. R. Moore, Y. R. Xiong, J. Gu

"Sand is a naturally occurring granular material that is a result of the physical or chemical breakdown of rocks. Raw/natural sand contains various minerals, and it is this combination of minerals that brings the value to the construction aggregate industry. However, it is the quartz component of sand that is valued in its application as industrial silica in glass, high purity quartz, foundry sand, and oil and gas fracturing. Depending on the industry, the grade requirements can be the concentration of SiO2, particle size or shape, as well as contaminants such as the heavy refractory minerals, clays, fines, and alkali metals. With the ever declining mineral feed grade, processors continue to face challenges making the industry specific concentrate grade. As such, it becomes more important to tailor make the processing reagents to fit the mineral, processing conditions, and desired quality specification. This paper focuses on the application of novel collectors towards the beneficiation of sand for each of the major industrial silica applications. INTRODUCTIONQuartz is a mineral composed of a framework of silicon and oxygen atoms. It is the second most abundant mineral in the Earth’s continental crust. There are many species of quartz, which are defined by the particle size, shape, and color. Silica sand is one of those species, which is the byproduct of the physical or chemical breakdown of quartz containing rocks or crystals. Geologist define silica sand as a silica mineral with a particle size between 0.05 and 2 mm in diameter (Zdunczyk, 2001). Silica sand has significant value to society in recreation (beach sand and toy boxes), construction aggregate (concretes and asphalt), industry (iron & steel casting, fracturing proppants, and glass), as well as specialty products such as semiconductors or silicon wafers used in electronics.The aggregate business is the dominant consumer of silica sand products. Conversely, glass making, foundries (casting material), abrasives, and fracturing proppants are the dominant applications for industrial silica sand. Not much beneficiation is required for sand products going into the construction industry, other than sizing and scrubbing to remove clay. However, the industrial silica sand applications are dependent on particle size, shape, and degree of contaminants, which sets the market value (table 1). Therefore, as the more specialty products are produced, more sophisticated techniques and chemistry need to be applied to ensure the appropriate quality is met."

Jan 1, 2018

By S. M. Javad Koleini

Processing of phosphate ore sample was investigated for increasing phosphate content and reduction of its gangue minerals such as carbonates and silicates. Experimental designs were per-formed using Taguchi method. Different flotation methods were investigated for Moundon phosphate ore sample and three methods were used as follow: direct cellophane flotation, reverse calcite flotation and reverse quartz flotation. Because of the sensitivity of cellophane flotation to slime content, prior desliming was carried out before the experiments. Direct flotation experiments carried out and a concentrate contained 23.80% P2O5, 6.88% SiO2 and 72.33% recovery were produced. The achieved P2O5 content in the produced concentrate from reverse flotation of calcite was 26.44% and the recovery was 82.56%. The concentrate products obtained at optimum conditions by direct flotation of phosphate and indirect flotation of calcite were subjected to indirect flotation of calcite and direct flotation of appetite and final concentrates with P2O5 grade of the order of 24.19% and 26.96% were obtained, respectively. It was concluded that one stage direct flotation is unavoidable to achieve a product with low SiO2 content.

Jan 1, 2014

By Josefin Lannefors, Anders Klingberg, Natalija Gorochovceva

"Development of new anionic collectors becomes more and more important. This can be explained, on the one hand, by the fact that over the years phosphate ores have become more fine grained and complex (example weathered). On the other hand, a development with a focus on sustainability (sustainable development) of new anionic surfactants is required by authorities and society. Within the sustainable development several characteristics of a collector have to be taken into an account: efficiency, selectivity, froth characteristics, environmental profile, raw materials used for the synthesis, manufacturing complexity, stability upon storage, etc.Several anionic surfactants based on ester and amide chemistry were synthesized, characterized and used as flotation agents for calcium phosphate containing ore. The surfactants were used in a formulation together with other anionics, since in a pure form, during the flotation, they did not provide right froth characteristics.A new anionic collector/formulation was developed, that fulfills all above listed requirements."

Jan 1, 2014

By Andrzej Luszczkiewicz, Alicja Bakalarz

The application of new collectors is considered to improve the beneficiation of Polish sedimentary complex copper ores from the Legnica-Glogow Copper Basin (SW Poland), the upgradeability of which becomes more difficult because of ores grade declining. One group of potential collectors is represented by nonpolar reagents. According to the available literature data, only selected sulfides float in the presence of the nonpolar liquids. The paper presents laboratory scale flotation results for the main sulfide minerals occurring in the Polish copper ores applying either thiol (potassium ethyl xanthate) or nonpolar (aqueous emulsion of n-dodecane) collectors. The investigated feed contained 1.91 % Cu in the form of sulfide minerals such as bornite, chalcopyrite, chalcocite and covellite. Other sulfide minerals including galena, pyrite and sphalerite were also present in the samples. Several flotation tests with various doses of each collector were conducted. Mineralogical analyses of flotation products were carried out and the results compared. A comparison of the results indicated that all sulfide minerals floated well with high recoveries ranging from 91 % to 99 % in the presence of the thiol collector. The use of the nonpolar collector provided results in flotation of sulfide minerals with different terminal recoveries from 61 % for chalcopyrite to 100 % for sphalerite. The most significant differences in flotation in the presence of both types of collector under various conditions of upgrading were observed for chalcocite, chalcopyrite and covellite. Similar flotation results were observed for sphalerite and galena for both collectors. The studies confirmed selective flotation of sulfides from the copper sulfide ores of the Legnica-Glogow Copper Basin in the presence of nonpolar collectors.

Jan 1, 2014

By Carlos de F. Gontijo

The flotation of quartz particles was studied over the particle size range from 0.5 µm to 1000 µm and for advancing water contact angles between 0º and 83º. Flotation was performed in a column and in a Rushton turbine cell. Particle contact angle threshold values, below which the particles could not be floated, were identified for the particle size range 0.5~1000 µm, under different hydrodynamic conditions. The flotation response of the particles, either in a column or in a mechanically agitated cell with a similar bubble size, was comparable. Turbulence plays a role, as does bubble-particle aggregate velocity and bubble size. The stability of the bubble-particle aggregate controls the maximum floatable particle size of coarse particles. For fine particles, the flotation limit is dictated by the energy required to rupture the intervening liquid film between the particle and bubble. Flotation of very fine and large particles is facilitated with small bubbles and high contact angles. These results greatly extend our earlier observations and theoretical predictions.

Jan 1, 2014