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By Y. Y. Li, Q. Chen, Y. X. Cai, Q. Zhang, S. Mao

"Due to the influence of combustion conditions, the fly ash produced by some power plants has the problem of high-carbon content. The unburned carbon in fly ash can be removed by flotation, and the decarbon tailings should reach the national standard level I fly ash. The fineness of the requirement is one of the important indicators and is also an important factor affecting the tail ash activity. In this paper,adopting two methods investigate the effect of particle size on the flotation index: one is direct flotation of fly ash, and the other way is wet grinding + flotation of fly ash, comparing the two methods and selecting the appropriate process,which provides a way for the effective utilization of fly ash. INTRODUCTION Fly ash is a solid waste discharged from coal-fired power plants. The annual amount of emissions of fly ash are very large in China. The amount of fly ash were discharged from coal-fired power plants are increasing gradually, and the amount of fly ash stored has exceeded 2.5 billion tons, but the comprehensive utilization of fly ash is not high, which brings about a huge environmental problems( Lu et al.,2011). Carbon is a harmful component of fly ash in cement and concrete application (Zhang et al.,2008). Fly ash decarburization is an essential link to improve the utilization efficiency of fly ash and the reduce pollution ( Yang et al.,2012). Carbon is selected from fly ash to make full use of fly ash resources and improve utilization of fly ash (Li et al.,2008). In this paper, the flotation decarburization of high-carbon fly ash is studied, through comparing the grinding and not-grinding processes, optimizing the separation process of fly ash, which provides a way for the effective utilization of fly ash."

Jan 1, 2018

By F. K. Ikumapayi

An approach to environmental sustainability and improved process economy, in sulphide minerals production is recycling of process water in flotation of complex sulphide ores, although the chemistry of process water may be a critical issue to flotation efficiency. The influence of major components of calcium and sulphate ions in process water on xanthate collector adsorption and flotation response using pure chalcopyrite, galena and sphalerite minerals were investigated by Hallimond flotation, zeta-potential measurement, FTIR and XPS spectroscopy studies, while bench scale flotation tests were also carried out using complex sulphide ores. The impact of the species in flotation was comprehended using deionised water, tap water, process water and simulated water containing equivalent amount of calcium and sulphate species in process water. Hallimond flotation results showed a decrease of chalcopyrite and galena recovery in process water and also in the presence of calcium and sulphate ions in both deionised and process waters, whereas sphalerite does not respond to flotation. The adsorption of calcium and metal ions but not sulphate ions on the minerals is evidenced by zeta-potential data. FTIR and XPS studies revealed the presence of surface oxidized sulfoxy species and surface calcium carbonates on chalcopyrite in the presence of process water and water containing calcium ions, surface oxidized sulfoxy and carbonate species on galena in the presence of deionised water, process water and water containing calcium and sulphate ions, all at flotation pH 10.5, and these surface species influenced xanthate adsorption. The presence of surface oxidized sulfoxy and carbonate species at the sphalerite flotation pH 11.5 were seen in the presence of deionised water, process water and water containing calcium and sulphate ions, but the surface species does not influence xanthate adsorption. Bench scale flotation using two different complex sulphide ores showed that chalcopyrite, galena and sphalerite recoveries are better in process water than tap water. The studies showed that the process water can be recycled in flotation with no detrimental effect on grade and recovery of sulphide minerals. Keywords: sulphide minerals, flotation, zeta-potential, FTIR, XPS

Sep 1, 2012

By S. Patra, R. Venugopal

"The quality of pellets produced is affected by quality anssastd quantity of green pellets, amount of addition of binders, type of binders added, amount of moisture added along with the other variables like rotation, inclination and fineness of feed. The green pellet quality depends upon chemistry, mineralogy and granulometry of fines used for pellet making, the feed size, its moisture content and porosity. During firing of green pellets ingredients present within reacts to form different phases and microstructure. So in turn physical and metallurgical properties of pellets are influenced by amount and type of binder and flux addition, induration time and temperature. During iron making process, the metallurgical properties of fired pellets are decided by the type and amount of these phases and their chemistry. Green pelletizing and induration studies have been already carried out with hematite ore fines. Indian iron ores of high alumina content showing different pelletizing characters, these studies can’t be directly interpreted. The main objective of proposed research work is to understand the green pelletizing process and determine the water bentonite interaction at different levels. Detailed investigation on swelling behavior of bentonite and microstructure of the green pellets of iron ore fines from SAIL captive iron ore fines from the Barsua in the state of Odisha. To convert these ore fines into pellets, the key raw material, additives and process variables that influence the pellet quality needs to be identified.INTRODUCTION Pelletization is the unit operation of agglomerating iron bearing fines (generally below 150µ with 65-80% passing 40µ) by tumbling in horizontal rotating drums or inclined discs, (Sivrikaya and Arol, 2013; Bhuiyan et al., 2011; Forsmo et al., 2006; Sastry et al., 2003) and the pellets are approximately spherical lumps formed by this process in presence of water and binder, on subsequent induration at 1300°c (Sivrikaya and Arol, 2014; Sivrikaya and Arol, 2013; Sivrikaya and Arol, 2012; Sivrikaya and Arol, 2010; Sastry et al., 2003; Kawatra and Ripke, 2003; Iveson, 2001a; Iveson, 2001b)."

Jan 1, 2018

In this study, selective flocculating of diaspore using anion macromolecular reagent as flocculant was tested to separate diaspore from alum-silicate minerals. Firstly, the effect of pH on settling behavior of diaspore and kaolinite dispersions has been investigated. The results show that the maximum settling speed of diaspore and kaolinite appeared re-spectively at pH7 and pH3.33 which is close to the point of zero charge (PZC) of diaspore (6.8) and kaolinite(3.5). This result is in well agreement with the double electric layer theory. Secondly, the settling behavior of diaspore and kaolinite particles in different anion flocculant solution have been researched. The results indicate that flocculant solution concentration significantly affect the selectivity and the flocculating performance of anion molecular. In high concentration solution, both diaspore and kaolinite have faster settling rate compared to blank solution. How-ever, in low concentration solution, the anion macromolecular can enhance the settling rate of diaspore remarkably but has no apparent effect on the settling rate of kaolinite. This result suggests that the tested anion flocculant is a promising reagent for de-silica of diasporic bauxite. Lastly, FTIR method was employed to probe the adsorption mechanism of flocculant on diaspore and kaolinite. The results reveal that there are anion flocculant characteristic bands on the spectra of diaspore but no obvious characteristic bands of flocculant on the FTIR spectrum of kaolinite. This result is in good correspondence with settling test.

Jan 1, 2014

By Y. S. Li

The life cycle assessment method is applied to investigate the environmental impacts of cop-per-slag and copper-ore concentration process. Some environmental load data of copper production are obtained. The result indicates that damage level of human health, ecosystem quality and re-sources respectively is 0.174, 0.0203, 0.246 in the copper-slag concentration and 0.112, 0.0136, 0.299 in the copper-ore concentration. Environmental impact of copper-slag production (0.44) is more than that of copper-ore production (0.42), but can meet the environmental protect demand. With domestic copper concentrate supply gap enlarging, recovering copper from slag will lead to a significant improving of resource utilization and development of circulation economics.

Jan 1, 2014

By D. Tang

The froth zone in a flotation cell is recognised as a region which contributes to the overall flotation performance. Froth recovery is a measure of the efficiency with which the froth phase delivers particles arriving at the pulp-froth interface to the concentrate. Poor froth recovery in scavenger stages is generally attributed to poor froth stability. The key indicators of froth performance: froth recovery, entrainment and water recovery were measured in an OK3 pilot cell installed at a zinc concentrator in Australia and supplied with scavenger feed. Cell hydrodynamic and pulp chemical conditions during the operation of the cell were also measured as well as bubble growth across the froth phase. The objective of the work was to assess the impact of a number of commercial frothers on the froth performance in the OK3 cell and assess the suitability of using bubble growth as an indicator of froth stability.

Jan 1, 2014

By M. Mirnezami

Pentlandite samples were obtained as Ni concentrate from three Canadian plants and one specimen sample from Ward?s Scientific Establishment. The samples were upgraded using gravity and magnetic separation techniques. Nickel concentration was determined by atomic absorption spectroscopy. Microprobe analysis identified a range in Co and Cu lattice substitutions. All samples exhibited similar zeta potential-pH trend with isoelectric points from 2 to 3, and similar responses to copper activation and addition of xanthate. The similar trends indicate that the variations in lattice substitution identified have no significant effect on electrokinetic properties; that is, samples from any source likely yield results that can be generalized.

Sep 1, 2012

By R. S. C. Smart

Surface chemical factors, including the balance of hydrophobic (e.g. collectors) and hydrophilic (e.g. oxidation products, precipitates) species, are major control determinants in flotation rates of specific minerals and therefore grade and recovery. There are a number of challenges involved with the surface analysis of different mineral phases from process streams in a flotation facility. The first is to collect samples that are representative of the process and retain their surface chemistry prior to introduction into the instrument. The second challenge in studying the surface chemistry of specific minerals is to find reliable methods of mineral phase recognition. In surface analysis of mineral particles, confident mineral selection can be difficult with many multi-metal minerals and with precipitated, adsorbed, reacted and contaminant species in the outermost molecular layers. The third challenge is to provide a statistical surface analysis of multiple grains of the same mineral. Methods to achieve these aims are described. Principal component analysis (PCA) of ToF-SIMS data provides improvement in phase recognition, particle selection and associated variations in surface species. Specific examples from both lab and plant operations, demonstrate that this technique can be utilized to differentiate surface chemical factors promoting (hydrophobic species) or inhibiting (hydrophilic species) flotation. A study of copper ion transfer (inadvertent activation) from chalcopyrite to pyrite and sphalerite clearly identified a statistical difference in copper intensities between the sphalerite and pyrite phases corresponding to their flotation response. The PCA analysis applied to concentrate and tails samples collected from the Inco Matte Concentrator demonstrated extensive CuOH and NiOH transfer between chalcocite and heazlewoodite minerals. The statistical analysis has been able to identify mechanisms controlling recovery and selectivity. High intensity conditioning (HIC) tests in which sphalerite was separated from a complex sulfide ore gave a 5% increase in the overall Zn recovery. The PCA/ToF-SIMS statistical analysis revealed the discriminating depressant action of adherent aluminosilicate (gangue) fine particles and adsorbed ions on the surface of sphalerite grains. HIC conditioning resulted in the removal of these gangue fines improving surface collector attachment efficiency.

Jan 1, 2014

By W. Y. Gao

Diaojuntai Concentrator adopts a process of low intensity and high intensity magnetic separation and anionic reverse flotation, with all the concentrate from magnetic separation being treated by re-verse flotation to obtain a qualified final concentrate. The high reagent cost and energy consumption of the reverse flotation have led to a high concentrate cost. The test research on reducing the feed to the reverse flotation was therefore carried out. Based on the study of the properties of the ore sample, the concentrate of low intensity magnetic separation was screened at 0.076 mm and the undersize fraction was concentrated by concentrator with gravity and magnetic field. The results show that a qualified concentrate can be obtained at various rising current rate, pulsating current and power-on style, with the operation rate over 85%. The extraction of some part of qualified concentrate from the concentrate of low intensity magnetic separation by magnetic separation can reduce the feed to the reverse flotation by about 35% so as to reduce the production cost of concentrate.

Jan 1, 2014

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

By V. Sheikhzadeh, M. Saghaeian, R. Hejazi, A. Abazarpoor

"The morphology of pellet feed is known to influence several properties of iron ore pellets, including drop number, compression strength and reduction properties. The effect of grinding method on the particle size, specific surface area and particle shape of an iron ore concentrate has been studied. Grinding methods considered were ball mill and high pressure grinding rolls (HPGR). 5 different samples (Blaine= 1800, 1900, 2000, 2100 and 2200 cm2g-1) were used to compare the size, shape and specific surface of particles for each grinding methods. Particle size was meticulously examined by sieve analysis, laser sizing and image analysis. In samples ground by ball mill, it has been observed that the fraction of particles <10µm increases from 39% to 46% as the Blaine number increases from 1800 to 2200 cm2g-1. For HPGR samples, corresponding figures are 41% and 49% respectively. It is evident that for samples ground by HPGR, the fraction of fine particles is higher than that of those ground in the ball mill. To measure the specific surface area of particles, Blaine and BET were used. A higher real surface area was observed from HPGR treatment in comparison to ball mill grinding, provided by a higher porosity, cracks, roughness and new surfaces. Shape factor of particles was determined using three descriptors: circularity, roughness, and aspect ratio. It was also observed that particles produced by HPGR were more elongated, less circular, and rougher than those processed by the ball mill. 1. INTRODUCTION Particle size and shape are important parameters that can significantly affect mineral processing plants and pelletizing plant performances (Brozek and Surowiak, 2007). It has also been proposed that green pellet quality is directly related to the amount of fine particles in a pelletizing plant (Dwarapudi et al., 2008; Umadevi et al., 2008; Gul et al, 2014; Van der Meer, 2015). Particle size distribution and specific surface area (SSA) are also key factors that can control the quality of green and fired pellets. Processing circuits generally reduce the fines fraction to lower than the required specific surface area (SSA). It is therefore necessary to regrind concentrates to produce suitable pellet feed for further treatment in the balling and firing steps [1, 2]. Two main methods are used for re-grinding of concentrate; high pressure grinding rolls (HPGR) and ball mill. Given the different forces used to reduce size in these methods, it is expected the shape of particles will be different (Pourghahramani and Forssberg, 2005)."

Jan 1, 2018

By Ritva Tuunila, Antti Häkkinen

"Wet stirred milling is one of the most effective grinding methods in producing very fine powders in large scale production, but it is a very energy-intensive process, especially when pigments or even nanosize particles are produced. Therefore, optimization of the process parameters is important. The specific energy consumption is a function of stress energy, which describes the effect of tip speed and media characteristics on grinding, and is related to the number of stress events during milling. In effective grinding, a large number of stress events are necessary. The stirrer configuration influences the number of stress events and their intensity, because the motion of the media and the suspension are caused by a rotating stirrer. The effect of three different stirrer types: a pin, disc and blade stirrer, on the grinding rate, i.e. product fineness and specific energy were investigated in this study with a batch laboratory stirred mill with two tip speeds. The material used in the experiments was calcium carbonate. The results obtained with the smaller tip speed showed approximately similar grinding rates and energy consumption for all stirrer types. When looking in closer detail, the blade stirrer seemed to give the finest product with all grinding times compared to the pin and disc stirrers, which both produced almost the same product fineness with the same grinding times. The specific energy consumption was the smallest with the disc stirrer, but not very big differences were obtained. With a higher tip speed, greater differences occurred both in grinding rates and specific energy consumption. The blade stirrer was the most effective in grinding, and the pin stirrer the next. The net energy consumption for the blade and pin stirrers was almost the same, but it was slightly higher for the disc stirrer."

Jan 1, 2014

By S. M. Bradshaw, R. Smith, J. H. van Vreden, C. A. Snyders

"The re-treatment of gold tailing heaps has shown to be a potentially significant revenue stream for both large and small scale gold companies. Limited access to capital and lack of skilled labour remain restrictive especially when dealing with a refractory ore and/or where limited amount of material are available. Alternative techniques such as low temperature pre-leaching options to unlock value are therefore in demand. Several low temperature pre-leaching experiments in acidic and alkaline solutions, followed by cyanidation were performed which ultimately led to the further investigation of a caustic pre-leaching step. It was found that the Au recovery from a refractory ore tailings heap could be significantly improved from ˜ 15 to 20% to greater than 60% with a simple atmospheric NaOH pre-leaching step. It was further considered, that since the NaOH pre-leach liberate the Au associated with refractory sulphide minerals, the overall process may benefit by the inclusion of a froth flotation step to separate refractory sulphides from the free milling ore. Froth flotation on weathered tailing heaps are, however, known to be difficult, ultimately resulting in poor recoveries. A process flow sheet, incorporating a caustic pre-leaching step and a process which includes flotation and caustic pre-leaching of the concentrate, are technically evaluated and ultimately compared to simple cyanide re-processing. INTRODUCTION South Africa consists of a large number of gold tailings dumps. Janse van Rensburg (2016) estimated that there was about 517 dumps in the Gauteng area, covering approximately 320 000 ha of surface area. Recovering value from the dumps has received a great deal of interest but can be problematic due to the dumps often being refractory, preg-robbing and weathered. High recovery of valuable metals (Au and Ag) are possible (Fleming and Brown, 2010) but would most likely require pressure oxidation and subsequent neutralisation which can be very capital intensive demanding a high skill set to operate and maintain. In addition, these flowsheets target high processing tonnages due to the economy of scales at the lower grade feed materials, further increasing the capital requirement."

Jan 1, 2018

By L. Ya Agapova

Emissions from pyrometallurgical processing of copper concentrates are usually subjected to wet scrubbing. The washing sulphuric acid so produced contains up to 0.2 g/L of rhenium, which is recovered by solvent extraction in the form of crude ammonia permeate (NH4ReO4). The mother liquor, obtained from the sulfuric acid wash, contains up to 35 g/L of rhenium and significant amounts of impurities. Crude rhenium salt is commonly processed by double recrystallization to produce marketable salt. A ton of high grade NH4ReO4 can be produced using 3.0-3.5 m3 of mother liquor. We propose an efficient technology of mother liquor pre-treatment aimed at removal of water-soluble organics with subsequent electrodialysis. Electrodialysis of mother liquor in a multichamber electrodialyzer resulted in the production of pure rhenium acid, from which a marketable NH4ReO4 is precipitated using ammonia solution. Multiple steps of recycling consisting of dissolution of NH4ReO4 salt, rhenium acid production from NH4ReO4 salt by electrodialysis and precipitation of NH4ReO4 from rhenium acid made it possible to upgrade the purity of obtained rhenium compounds by 1-2 orders of magnitude. A rhenium metal powder of 99.997% purity was produced by high-temperature reduction of high-purity NH4ReO4 with gaseous hydrogen. Rhenium metal powder of high purity can be produced from sulfate solutions of NH4ReO4 by non-platinum anode-based membrane electrolysis processes also. Keywords: rhenium, mother liquors, membranes, electrodialysis, rhenium acid, ammonia perrhenate, reduction, powder, electrolysis

Sep 1, 2012

By A. V. Bogdanovich

In diamond ores processing, final waste tailings size, rejected to dump, is one of the most important parameters. On one side, it is necessary to minimize losses of diamonds, whose size exceeds 1 mm, on the other side ? to provide for the plant high throughput and sufficiently low capital and energy costs, which is in greater part connected with disintegration process. Extensive laboratory, pilot-scale and commercial-scale dressability studies of different types of diamond ores have been performed at JSC ?Mekhanobr Engineering? in recent years. With that, special consideration was given to determination of the required ores? disintegration size that would provide for a high recovery of diamonds. In diamond ores processing, in order to exclude breaking of large diamonds, stage disintegration is used with regrinding of light fractions and heavy fraction X-ray fluorescent separation tailings. On account of rather weak bonds of diamonds with enclosing minerals, in crushing and grinding of diamond ores, selective disintegration takes place, with aggregates? breakup along plane surfaces of least bonding, which facilitates liberation of diamonds and their transition to free state. Heavy components losses with different sizes of final dump tailings were studied in processing of large samples. It was established, that in order to almost completely exclude losses of heavy components over 1 mm size, light fractions had to be ground to 2.5-3 mm size, while X-ray fluorescent separation heavy tailings of -15+3 mm size do not contain diamonds larger 1 mm in aggregates, and their regrinding does not increase total recovery of diamonds. On the basis of the conducted studies, relationships regarding heavy components and diamonds losses with respect to diamond ores final disintegration size were obtained, providing for more rational organization of the ores disintegration and processing flow sheet. Keywords: diamond, waste tailings size, disintegration process, recovery of diamonds

Sep 1, 2012

By S. Jagdish

India ranks fourth in the world of iron ore production and exported 55% of the total iron ore production of 180.9 million tons in 2006-07. As per United Nations Framework Classification (UNFC), the total iron ore reserves in India is 25249 mt. This consists of about 14630 mt of Hematite ore and 10619 mt of Magnetite ore. While the deposits of magnetite iron ore are limited to the states of Karnataka, Andhra Pradesh and Tamil Nadu, hematite ore is available in abundance in Jharkhand, Orissa, Chhattisgarh, Karnataka and Goa. National Steel Policy, declared by government of India in 2005 envisages 110 million tons of steel production by 2020. This is likely to be revised upwards. Massive exploration work in iron ore is needed to convert the available resources of iron ore into reserve category. Steel Authority of India Limited (SAIL) produced more than 24.5 million tons of iron ore during 2006-07 and plans to produce 42.0 million tons per year by the year 2010-11 to meet the requirement for a hot metal production of 26.2 million tons. While processing iron ore, the challenge faced would be the reduction of the gangue materials ? alumina and silica. It is proposed to bring down alumina and silica in the iron ore to less than 2% each from the current level of 2.5%~3.5% each. Appropriate beneficiation schemes are being developed depending upon the mineralogical characteristics of iron ores at different mines in the country. The state-of-art beneficiation technologies like Hydro-cyclone, jigging, magnetic separation etc. will be incorporated. SAIL?s corporate plan envisages blast furnace burden of 15% iron ore lumps, 15% pellets and 70% sinter by 2010. This strategy opens up the opportunity of utilization of micro fines generated in the mining and beneficiation processes for pellet making. This also directs towards all together new technological approach to the beneficiation process. SAIL is planning to set-up three pelletisation plants of 2~3 mtpa capacity. Environmental issues like reduction in slime loss and utilization of dumped low-grade iron ore are very important. R&D Centre for Iron and Steel, SAIL has carried out extensive laboratory investigations in the above area. This will help in reducing the loss of valuable iron through slimes and also increase the iron ore resource base. Laboratory investigations indicate that low grade dumped ore fines with Fe: 55.5% can be upgraded to a product with Fe: 66.2% with about 48% recovery.

Jan 1, 2014

By T. Wajima

"A novel carbonaceous immobilizing agent for heavy metal contaminated soil was prepared from rice straw using sulfur immersion and pyrolysis, and the lead immobilization in artificial contaminated soils using sulfur-impregnated carbonaceous material was estimated. The rice straws were cut to 1 cm pieces, and then immersed in 0.1 - 1 M K2S solution for 0 - 24 h to prepare sulfur-immersed materials. The immersed-materials were heated at 400 oC for 1 h in nitrogen gas to produce the sulfur-impregnated carbonaceous material by pyrolysis. The abilities of the product to immobilize lead from aqueous solution were examined to obtain the product with high lead immobilization ability. With increasing K2S concentration, the immobilization ability of the product for lead gradually increases and then above 0.5 M K2S those are almost constant, while 15 min is sufficient for the immersed time to obtain the product with high lead immobilization ability. The product prepared from material immersed in more than 0.5 M K2S solution for less than 15 min has a maximum immobilization ability for lead ion. The lead immobilization using the sulfur-impregnated product is sustainable due to the formation of leadhillite [Pb4SO4(CO3)2(OH)2] and anglesite [PbSO4]. The product can immobilize lead ion in various artificial lead contaminated soils. By mixing artificial lead contaminated soil with the sulfur-impregnated product, the eluted solution became neutral, and the eluted concentrations of lead ion dropped below the Japanese elution standard for soil.INTRODUCTION Soil contamination with heavy metals is a worldwide problem. Accumulation of heavy metals in soils affect soil ecology, agricultural productivity, quality of agricultural products, water resources, and serious health problems for human and animal (Raicevic, et al., 2005). In the United States, for example, approximately 63 % of the sites on the National Priority List (NPL) for the treatment of contaminated soils are contaminated by metals, and lead is the most common metal, found at 15 % of the sites. In Japan, according to a report by the Ministry of Environment, 43 % of the contaminated sites that exceed the environmental quality standards are contaminated by lead compounds. Soil contamination by lead compounds is also prevalent in other developed and developing countries where lead compounds are used extensively in industrial activities without careful contamination management. Lead is a ubiquitous heavy metal pollutant in soils due to their use widely. The primary sources of Pb contamination include industrial activities such as mining, smelting of metals, and the use of Pb-containing products such as paints, lead-acid batteries, bullets, gasoline and pesticides (Cao, et al., 2009). It can damage human nervous (especially children) and reproductive systems (ATSDR, 2007). The high concentration of Pb in the soil poses risks to human and animal health by the leaching of metals from the soil into water and the consumption of edible plants growth in the contaminated soil. Therefore, proper remediation is necessary to reduce metal availability in soil for protecting human health."

Jan 1, 2018

By C. Hazotte, M. -O. Simonnot, V. Houzelot, B. Laubie, M. Guilpain, B. Jally

"More than 400 plants in the world are able to accumulate nickel (Ni) in their aerial parts at concentrations higher than 10 g per kg of dry biomass. Then, Ni can be recovered from the biomass of these hyperaccumulator plants. Agromining is a chain consisting in growing such plants and producing metal. It has been developed thanks to the combined know-how of agronomy and hydrometallurgy. Hydrometallurgical processes have been designed; two different pathways were developed: i) acid leaching of ashes after biomass combustion and ii) direct Ni water extraction after biomass grinding. Experiments with 2 species of Ni hyperaccumulators (A. murale from the Balkans and R. bengalensis from Malaysia) have shown that the first process is very robust and transposable. For the second one, the way Ni is stored in the plant has a strong influence on extraction. A. murale transformation was explored in more details from the lab scale to the pilot scale. Results proved that Ni is totally transferred into the aqueous phase after 2 hours at 90 °C. A life cycle assessment has clearly shown the environmental interest of this approach (especially by detoxifying agricultural soils). INTRODUCTION Agromining is an emerging phytotechnology aiming at recovering metals thanks to hyperaccumulating plants (van der Ent et al., 2018). These plants are able to accumulate very high concentrations of metal in their aerial parts. For example, for nickel, the hyperaccumulation threshold is 0.1%, i.e. 10 grams of metal per kilogram of dry biomass. There are some advantages to use this technology instead of conventional mining techniques: •,Treating unconventional metal resources: they can be (i) natural soils with low concentrations but also low fertility because of the metal presence (like serpentine soils for Ni) (Bani et al., 2015), (ii) mine tailings or (iii) industrial wastes (like surface treatment sludge) after soil construction (Rue, 2017);"

Jan 1, 2018

"A sulfide ore containing 2.19 g/t Au and 13.13 g/t Ag was studied for the deportment and extractive metallurgy of pay metals. The ore is composed mainly of non-sulfide minerals with approximately 10% pyrite and minor amounts of marcasite, chalcopyrite, galena, sphalerite, and arsenopyrite. The deportment study using a comprehensive approach showed that gold and silver minerals in the ore are mainly native gold (Au), electrum (Ag, Au), petzite (Ag3AuTe2), hessite (Ag2Te) and volynskite (AgBiTe2) with minor amounts of acanthite (Ag2S) and argyrodite (Ag8GeS6). At current grinding fineness (P70@150µm), the majority of liberated native gold and electrum particles are larger than 20µm with 85% >40µm, some of them are even larger than 150µm, indicating that extended leach time may be required to dissolve these coarse gold grains to completion and gravity concentration needs to be considered. Petzite is relatively fine with all liberated particles being less than 80µm in size. Gold distribution and leach testwork results showed that liberated gold accounts for 50% of the head assay, exposed gold associated with sulfide and non-sulfide minerals accounts for 30% and 11% of the head assay, respectively. Gold locked in sulfide and non-sulfide accounts for 4.8% and 4.1%, respectively. Thus, it is recommended that cyanide leaching be considered for extracting gold in this ore. This paper presents the detailed results of the gold and silver deportment study and extractive metallurgy testwork, and discusses the impact on process selection and flowsheet development.INTRODUCTION Gold and silver have been found in various geological environments and ore types. In terms of the gold deportment and extractability, gold ores can be classified into two categories and 12 types. Their extractive metallurgy is largely driven by mineralogical factors such as particle size, association with other minerals, coatings and rimmings, presence of cyanicides, oxygen consumers and preg-robbers, presence of refractory gold minerals and locking of submicroscopic gold in sulfide and sulfarsenide mineral structures (Zhou et al., 2004; Marsden & House, 2006; Zhou, 2013a, 2013b). Compared to gold, silver mineralogy is more complex and metal extraction is more challenging due to its presence in over 200 Ag-bearing minerals (a silver-rich ore body would typically contain 5 to 10 different silver minerals) (Gasparrini, 1984), presence of refractory silver minerals (such as pyrargyrite, prustite and stephanite) and submicroscopic silver in sulphide minerals (such as galena and copper minerals) (Chryssoulis et al., 1985; Di Prisco et al., 2002). The presence of these issues often causes problems in Ag-bearing ore processing. Therefore, knowing the deportment of gold and silver in the ores and metallurgical products is important for flowsheet development and process optimization."

Jan 1, 2018

By B. Y. Tuo

This article presents results of studies performed to determine the feasibility of using low-grade limonite ores from Yunnan deposit. Laboratory tests and commercial trials have shown that the magnetic separation can be performed with a high high-grade concentrates. The quality of the preparation concentration meets the requirements for blast-furnace smelting. The results as a whole demonstrate the feasibility of utilizing bank limonite ore. Yunnan limonite?s magnetic separation, roasting magnetic separation and flotation experimental study shows that grade of the ore grade can been from 32.91% heighten to 58.64%, a recovery of iron is 90.87%, productive rate is 51% through orthogonal test optimization; roasting magnetic separation can obtain that the grade of iron preparation concentrate is 61.16%, recovery is 67.39%, productive rate is 36%. As far as economy and enviormental protection is concerned, strong mag-netic suggested a more appropriate process. Keywords: Limonite; Roast; Magnetic separation

Jan 1, 2014