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By David G. Hulbert, Daniël J. Oosthuizen, Bernard Muller, Daniël de V. van der Spuy

"OVERVIEWExpert Online is a software system that aims to mimic an informed expert on a minerals processing plant. The primary objective of Expert Online is to provide operators with effective training and on-the-job assistance. Training will mostly be done off-line (e.g. using simulators of the plant), while on-the-job assistance will help the operator during normal operation to run the plant in an effective manner. Although Expert Online focuses on the operator, it is expected to also be of value to other plant personnel, including supervisors and plant managers.Expert Online will make use of novel artificial intelligence technology (developed by MINTEK) known as the Interpreting Expert System (IES). Previously the IES was only able to explain the actions taken by the controller. Expert Online will extend this functionality to also take the process dynamics into account.Expert Online is being developed by a South African consortium comprising MINTEK (focusing on the research and development of the system as a whole), Lonmin (globally one of the biggest platinum producers, with plants suitable to test Expert Online on) and the University of Natal (academic partner, providing consultation and focusing on complex process modelling). The initial application of Expert Online will be on milling- and flotation plants.This paper discusses the structural design of Expert Online for implementation on the latest version of MINTEK’s open control platform, PlantStar, as well as several advances and additions since the previous implementations of the Interpreting Expert System."

Jan 1, 2003

By N. ??dyanik, Z. Kugukaldinova, O. Mishurina, Y. Glazkova, E. Mullina

"This paper describes the process flow of a selective processing method for acidic mine waters formed in the copper sulfide industry and characterized by a high content of copper, iron, and manganese ions. The proposed method comprises a series of sequential processes: the 1st stage is the recovery of Cu2+ ions by precipitation, the 2nd stage is the recovery of Fe2+ and Fe3+ ions as a dispersed phase by acid-base precipitation, followed by recovery in the 3rd stage of Mn2+ ions by converting Mn2+ with an oxidizing agent into insoluble forms of manganese and subsequent recovery of the dispersed phase by electroflotation. The developed method was tested on the acidic tailing storage facility (TSF) water of a mining project in the Urals region. The practical results of the implementation of the developed method have shown that its implementation will allow to recover copper, iron, and manganese in the form of salable products with a simultaneous decrease in their concentrations in adjacent water bodies down to the applicable MPCs. The process is a simple one, does not require any sophisticated expensive equipment and can be implemented either as a standalone solution or as part of existing treatment facilities. INTRODUCTION As a result of unsustainable utilization of natural resources in Russia, only a small fraction is processed into commodity products, while the rest is systematically dumped as emissions, effluents, and other wastes, polluting the environment. By amount of waste and concentration of valuable components, those wastes can be classified as aqueous technogenic resources [1, 2]. Therefore, the development of processing methods for this mineral resource category is an urgent and priority task that will significantly improve the industry’s profitability and the environmental conditions in the respective regions. MATERIALS AND METHODS Following research methods were mainly applied in this study: lab-scale and pilot-scale tests in a diaphragmless two-chamber electric flotation cell; for solutions and recoverable process products — chemical analysis using photometric determination techniques for metal cations and atomic adsorption determination techniques for the processing products. The phase composition of the precipitates formed in the process was investigated by X-ray phase analysis in the general-purpose diffractometer with a copper anode DRON-1."

Jan 1, 2018

By M. Z. He

Attractive particle interactions which underpin the sliming of gangue mineral particles onto valuable mineral phases are encountered in a number of flotation circuits. Sliming leads to poor flotation recovery of the valuable minerals and high recovery of the gangue particles in the concentrate. To mitigate sliming, low molecular weight poly-electrolytes are commonly used as dispersants during pulp conditioning prior to flotation separation of the valuable and gangue mineral phases. In the present work, the sliming mechanism of sericite onto chalcocite and the influence of interfacial chemistry and two anionic copolymer dispersants (carboxylate substituted polyacrylamide, polymer Cyquest 3223 and sulfonate substituted polymaleic acid, polymer P80) on the sliming interactions were probed in the pH range 5~9. It was shown that the sliming occurred under solution conditions where both chalcocite and sericite particles were negatively charged, as evidenced by their apparent particle zeta potentials. The suspension pH had a profound effect on sliming process as the extent was markedly greater at lower than higher pH. The sliming was found to be due to the chalcocite dissolution, Cu (I) release and oxidation to Cu (II), followed by hydrolysis and specific adsorption, leading to sericite particle surface charge reversal and the formation of electropositive sites on chalcocite surface in the pH range 5~9. Addition of polymer Cyquest 3223 or P80 not only increased the magnitude of zeta potentials of both sericite and chalcocite particles but also reduced the formation of Cu (II) ions and complexes, which mitigated the sliming behaviour. The adsorption of polymer Cyquest 3223 or P80 at 3 g polymer / kg solid or more had a significant impact on the zeta potentials of both sericite and chalcocite particles. Sericite-chalcocite particulate adsorption studies showed that sliming was completely suppressed via an electro-steric repulsion mechanism resulting from anionic polymeric dispersant adsorption at dosages > 3 g polymer / kg solid.

Jan 1, 2014

By P. S. Dash

With implementation of stringent environmental regulations, ultra clean coal technology development programs have gained significant importance worldwide. As far as Indian scenario is concerned, most of the coals present in India are of drift origin and low grade, containing high mineral matter varying from 15% to greater than 50%. The inorganic or ash constituents of Indian coals are finely disseminated through the organic or carbonaceous constituents so, that commonly used physical beneficiation techniques are of only limited value in affecting separation. Chemical processes involve addition of chemicals, which react with the mineral matter and allow its easy removal. The present study envisages the effect of aqueous alkali leaching followed by acid washing on the removal of mineral matter from two different captive coals of Tata Steel at elevated temperature and pressure. The experiments are conducted at desired conditions using a bench scale pressure reactor set up having proper data acquisition and control system. The research study revealed, that it is possible to reduce the ash content up to 70% by this method. The alkali content of the product clean coal does not increase whereas the silica and alumina content reduces by nearly 58% and 62% respectively. Significant reduction in the phosphorus content is observed after the acid treatment. The crucible swelling number of the feed coal improves after the treatment. The mechanism of demineralisation was evaluated by analyzing the coal samples before and after the alkali and acid treatment using scanning electron microscope (SEM). Because of the acidic nature of the silicates and aluminates, they dissolve into the NaOH solution and form sodalite. Sodalite is partially soluble in the alkali solution. The hydrates formed during alkali treatment are partially removed due to acid wash. This study in overall provides an insight into possible alternative methods of beneficiation for removal of ash from high ash Indian coals.

Sep 1, 2012

By J. Lindström, J. Hamuyuni, M. Lundström, J. Aromaa

"The rising demand for metals today, coupled with the scarcity of primary sources for raw materials threatens both technological advancements and industrial manufacturing. In order to meet the demand, metals and other resources trapped in waste streams, have to be harnessed. This philosophy supports circular economy, where metals and other resources are kept in a closed loop. The pickling acid recovery system of most stainless steel production is one such example where the dissolved metals such as iron, nickel and chromium are currently not completely recovered due to the limitations of the current technologies. The aim of this study was to assess the available metals recovery methods from extremely concentrated acids. The main aim is to simultaneously recover metals and keep sulphuric acid reusable in acid circulation process. From the available literature, the most promising methods were chosen for laboratory experiments. Based on experimental work, the results and observations of electrodeposition, solvent extraction, and freeze crystallization are provided. KEYWORDS Pickling acid, metal recovery, solvent extraction, cathodic polarization, Freeze crystallization. INTRODUCTION Pickling in stainless steel production is an essential surface treatment process (Regel-Rosocka, M. (2010); Agrawal and Sahu, 2009). It is applied for removing surface films such as oxides and chromium-depleted layers to improve the corrosion resistance and surface finish of steel (Regel-Rosocka, 2010). Whilst the process greatly improves the surface finish of the stainless steel, it generates large amount of used acid, containing dissolved metals including chromium, iron, and nickel (Agrawal and Sahu, 2009). Recovery of acid is common practice for most steel producing industries (Nyman and Koivunen, 1986). In this work, acid regeneration process is investigated so as to simultaneously reusing sulfuric acid and recovering the dissolved metals. Recovery of valuable metals even in very small amounts would also bring additional revenue to the steel production industry. At a time when metal production has also been challenged by lack of natural resources for raw materials, secondary sources for metals such as the acid pickling process therefore, have greater potential as supplements. From earlier studies, electrodeposition (Giovanardi and Orlando, 2011; Kuznetsov et al., 200; Rögener et al., 2012; Surviliene et al., 2006), solvent extraction (Alguacil and López 1996; Haghshenas et al., 2009; Kesieme et al., 2013) and freeze crystallization (Beyer et al.,2003; Hasan et al.,2017; Van der Ham et al., 1999) are some of the most established potential methods. Earlier studies have also shown that simultaneous recovery of acid and metals would require combination of different methods. This is primarily due to the nature of very stable metal containing complex compounds formed during pickling. These complexes must be broken down to free the metals for further recovery processes."

Jan 1, 2018

By S. F. Kaplan, A. S. Dolotov, V. N. Kovalev

"At this point in time, autoclave recovery (POX) followed by sorption cyanidation (CIL) is one of the most promising technologies for the efficient processing of refractory and double refractory gold-bearing sulphide rock. This hydrometallurgical technology requires the use of a large amount of water (up to 5 tons per ton of used concentrate), resulting in highly saline water with high pH (pH 9-11), high content of cyanides (up to 300 mg/l), arsenic compounds, antimony and a number of heavy metals. In order to determine the possibility of using recycling industrial water in POX-CIL technology, several batches of experiments were conducted (using the double refractory flotation concentrate of the Mayskoye deposit). Urban water with a chloride ion content of 10 mg/l was used during the reference POX-CIL experiment as the liquid phase of the ??? feed pulp. At that, gold extraction rate amounted to 89.4 %. A full cycle of POX(200 ºC)-CIL was carried out during the first part of the experiments; at that, fresh concentrate of the untreated recycling water with cyanide ion content of 95.4 mg/l, left after the completion of the previous CIL cycle, was used for repulping. It has been established that direct use of untreated recycling industrial water is impossible due to a sharp decline in gold extraction (preg-robbing) down to 79.5%. The presence of chloride ions, cyanide ions and other ligands in the liquid phase provides effective complexion formation for the recovery gold; complex gold compounds are quickly and firmly sorbed by the natural carbonaceous substances of the concentrate at the stage of autoclave recovery; they are virtually not cyanized onwards, and gold is carried over to the tailings. During the the second batch of experiments, recycling industrial water with cyanide and chloride ions' concentration of 500 mg/l each was subjected to the reverse osmosis desalination (up to 6 times in a successive order). After each desalting cycle, such water was used as the liquid phase of the feed pulp in POX-CIL. 6 cycles of RO desalination enabled the extraction of 86.1% Au (which is close to reference recovery). During the third batch of experiments, recycling industrial water was diluted with distilled water (2, 4, 16, 32, 64 times); after each dilution cycle, this water was used as the liquid phase of the POX-CIL feed pulp. Gold extraction after 64-fold dilution amounted to 82.6%. The results of the conducted researches show that the use of untreated recycling industrial water in POX-CIL hydrometallurgical technology is absolutely impossible due to a sharp decline in gold extraction. Even the 64-fold dilution with pure water is inefficient both from the perspective of gold extraction and of rational use of water. Reverse osmosis desalination solves the problem of water treatment except for the removal of cyanide ion, which requires separate reagent treatment of water."

Jan 1, 2018

By S. N. Titkov

Flotation of halite?new, recently begun to be developed method of processing water-soluble minerals. In the paper the results of studies of the new directions of the application of halite flotation are represented. Studies on the flotation separation of halite and sylvite in the salt solutions of different composition, showed the possibility of the halite flotation realization not only in the carnallite brine (content of salts: MgCl2 25.5% ~ 26.0 %, chlorides of potassium and sodium 5.5% ~ 6.0%), but in the sylvinite brine, which contains 10.5% ~ 10.8% KCl and 20.5% ~ 21% NaCl. On the basis obtained results are carried out experiences on the halite flotation from samples of the converted products of sylvinite ores by flotation method and by the method of the electrostatic separation. It is shown that in all cases it is possible to accomplish effective and selective recovery of halite. The halite recovery into the foam product of flotation makes 80% ~ 90% with an increase in the content of KCl in the cell product of flotation in comparison with a composition of flotation feed: - from the product after the electrostatic separation of ore ? from 76% KCl to 95% ~ 97% KCl; - from the small fraction of ore (- 0.25 + 0 mm) ? from 30% KCl to 60% ~ 64% KCl; - from middlings (intermediate products) of sylvite flotation from 16% ~ 31% KCl to 45% ~ 80% KCl. An increase in the molecular weight of alkylmorpholines increases the selectivity of the flotation separation of halite and sylvite. Halite recovery from small size fraction of ore or/and middling of sylvite flotation with the sub-sequent joint filtration halite product and tails of sylvite flotation allows to reduce considerably expenses for manufacture potash chloride from Pilot-industrial tests for the first time confirmed the possibility of the effective halite flotation in the saturated solutions of chlorides of potassium and sodium (sylvinite brine).

Jan 1, 2014

By Elena L. Chanturiya, Vladimir A. Bocharov, Roman A. Amosov

"In many volcanogenic base metal deposits of Russia the gold is closely associated with copper sulphides and pyrite. The recovery of gold associated with pyrite is especially difficult problem.Investigations of gold chemical state and mineral forms in copper-zinc sulphide ores of Gay and Barsuchiy Log deposits in the Urals have been made using EPMA, optic image-analysis, XRA, SEM, thermo-electrical force measurements and selective gold leaching experiments.Two gold varieties are determined: 1) free native gold particles (from 5 µm up to 0,25-1,0 mm), which can be liberated after grinding of ore up to 0,074 µm and named “free gold”; 2)”invisible” gold, including finely disseminated native gold and chemically bound gold. The second variety can’t be disclosed during grinding. Free gold can be recovered by gravitation and flotation while the processing behaviour of “invisible” gold is determined by properties of gold-bearing sulphides: pyrite and chalcopyrite. According to results of diagnostic leaching experiments in ores of deposits mentioned above the part by weight of free gold reaches 70%, the part by weight of the ”invisible” gold is up to 20%. About 10% of gold is enclosed in quartz and acid-soluble minerals.Theoretically (taking into account gold distribution data) it’s may anticipate gold recovery by gravitation up to 60%. However after grinding up to 50-60% of class –0,074 mm only about 40% of gold passes into oversize product including 30% of free gold and 8% of ”invisible” one. It can be recovered by gravitation. Remaining free gold and ”invisible” gold can be extracted by flotation – 25% in total. Inevitable gold losses in tailings may reach 8-10%."

Jan 1, 2003

By Mohammad Kor, David Beattie, Agnieszka Mierczynksa-Vasilev

The selectivity of polymer adsorption in mixed mineral systems is the basis for polymer depression of gangue minerals in flotation. Effective polymer depressants not only reduce gangue mineral recovery, they also have minimal effect on the recovery of the value phase, presumably through targeted adsorption on the gangue phase, and minimal uptake on the value phase. Traditionally, polymer depressant design has been guided by single mineral phase adsorption tests, with affinity and maximum adsorbed amount determined for gangue and value phases separately. However, there is a need to determine the actual extent of adsorption on the gangue phase while in the presence of the value phase. In this work, we report on the development of in situ atomic force microscopy (AFM) imaging for determination of polymer depressant coverage and morphology on mixed mineral surfaces. Our group has previously used AFM imaging on single minerals to connect adsorbed layer characteristics with bubble-particle attachment and flotation outcomes. Two sample types were used to test the methodology: (i) a mixture of two crushed/ground minerals encased in resin; and (ii) a composite mineral sample containing macroscopic regions of three different mineral phases. The samples have been used to probe the selective uptake of two modified dextrin polymers (octenyl succinate anhydride dextrin). AFM images acquired in situ (while all surfaces are immersed in the same polymer solution) of each mineral phase have revealed the natural selectivity of the polymer for the mineral surfaces. In all cases, the polymers adsorb on the all mineral surfaces present, but to a varying extent.

Jan 1, 2014

By Rebecca Hope, Derick Moolman, Frikkie Malan

"Despite the lip service that has been paid to pro-active plant maintenance processes over recent years, a significant portion of maintenance in industry is still reactive. The business driving force to prevent expensive production opportunity costs arising from “break-down maintenance” is obvious. Various benefits can be derived from successfully deploying remote equipment diagnosis technology and associated business processes.From an end-client’s viewpoint these include the ability to predict and take actions to prevent equipment breakdowns, increasing the lifetime of equipment by responding to appropriate operating instructions and therefore improving the return on capital expenditure. Better planning and scheduling of maintenance priorities and resources with performance measures like an Equipment Health Index are also possible. The knowledge that a qualified supplier engineer is constantly in touch with the operating conditions of their equipment, albeit remotely, is more than a comfort, and can be translated into quantifiable cost savings and improved supplier service levels.This paper analyses the reasons for the inadequate level of pro-active plant maintenance practice in industry today, and presents a number of important criteria in selecting appropriate solutions to this problem. A case study of a specific real-time, remote equipment management application is presented."

Jan 1, 2003

By Peng Qian, Xiao Li, Guoyan Fu, Peiwei Han, Yongliang Wang, Shufeng Ye

"Arsenic removal from high arsenic gold concentrate is conducive to increase the mineral value and realize the mineral comprehensive utilization. This study investigated the alkaline pressure oxidation leaching (APOL) of an arsenical gold concentrate in lower temperature to separate the arsenic into filtrate. The effects of temperature, NaOH concentration, solid-liquid ratio, reaction pressure and stirring speed on the leaching efficiency were investigated, and the characteristics of the gold concentrate and leaching residues were evaluated using XRD and SEM analysis methods. The obtained results showed that by using lower temperature (<60?) it is possible to avoid the production of elemental sulfur during the leaching process, which is benefit for the oxidation of arsenopyrite; When the reaction was carried out under appropriate conditions, more than 98% of the arsenic will be extracted into the filtrate as the form of arsenate or thioarsenate. INTRODUCTION In recent years, there has been considerable interest in the recovery of gold from refractory arsenical gold ore. The arsenic in this kind of ore usually exists as the form of arsenopyrite, and the gold surrounded by arsenopyrite exists as the form of fine particles, which will give many difficulties to metallurgical work. When the content of arsenic in the gold ore is more than 0.5%, it will seriously penalize the smelting efficiency (Ruiz et al., 2014). So pretreatment of the refractory gold ore is necessary to obtain the largest economic value and environmental benefits (Balaz et al., 2000). The oxidation pretreatment processes mainly include roasting oxidation, pressure oxidation, chemical treatment and biological treatment (Ann et al., 1992; Kou and Chen, 2012; Tongamp et al., 2010; Fernandez et al., 1995; Lin and Zheng, 1996). Among them, the roasting oxidation and pressure oxidation are the more ordinary processes in industry. The roasting oxidation process is the mature and adaptable technology, but the production of waste gas containing sulfur and arsenic will pollute the environment. The pressure oxidation method possesses certain metallurgical and environmental advantages, and can efficiently decompose the mineral. According to the different solution media, the pretreatment can be divided into alkaline and acidic pressure leaching pretreatments (Papangelakis and Demopoulos, 1990; Hiskey and Sanchez, 1995). The acidic pressure oxidation method has been used in most smelting plants for high arsenic gold ore pretreatment, while the alkaline pressure oxidation is still not widely applied. Compared with the acidic pressure oxidation, the alkaline pressure oxidation can be realized under lower temperatures."

Jan 1, 2018

By Tim Suljada, Mary Stewart, Jim G. Petrie, Damien Giurco

"The minerals industry is being challenged to reduce the amount of virgin ore that is mined, and to replace this material through the recycling of used commodity items and scrap, or by the reprocessing of waste materials. It is argued here that the existing technology base of minerals processing and refining offers real potential for handling these secondary resources. The challenge is to develop tools by which the most preferable recycling routes (both economically and environmentally) can be identified from a list of feasible alternatives, taking into account any operational constraints of these technologies.This paper describes an heuristic approach to developing the family of all technically feasible flowsheets to address this challenge, from which a preferred option may be selected according to a set of decision criteria (economic and environmental). Our approach uses conventional flowsheeting techniques of selecting flow variables and splitter functions, supported by design performance information for each unit operation. This set of design decision variables is augmented by knowledge of the suitability of a particular waste or scrap stream for a given unit operation within a flowsheet. We achieve this by comparing the composition of the scrap stream with the range of mineral streams for which the unit operation was designed initially. This is inspired by the “overlap” approach proposed by Legarth, where an “overlap” of 1 would suggest that there is high degree of compatibility between a given secondary resource stream and a primary mineral stream as inputs to a specific technology. The “overlap” concept has been extended to include information about the physical characteristics of secondary resource streams, as well as information relating to synergistic / antagonistic influences of minor elements present in the waste stream. A flowsheet which delivers a product of acceptable quality from a given secondary resource material is built up from a progression of unit technologies. The exercise is repeated to generate the family of all feasible flowsheets from combinations of acceptable unit technologies."

Jan 1, 2003

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 V. A. Ivanova, T. N. Perunkova, N. O. Dorozhanova, G. V. Mitrofanova

"Oxyethylated compounds are used as reagents-regulators in the flotation of non-sulfide ores, in particular, apatite-containing ores. Thus, the necessary degree of selectivity in the flotation separation of two calcium-containing minerals of apatite and calcite is achieved only by using, in addition to a collector, regulators-reagents from the nonylphenol ethoxylates class. In order to establish the most optimal structures, this paper presents a comparative assessment of the physical-chemical and flotation properties of several classes of oxyethylated compounds - alkylphenol ethoxylates, aliphatic alcohol ethoxylates and oxyethylated carboxylic acid. The authors have studied their dispergating ability with respect to the air phase and calcium soaps of the carboxylic collector. Dependences of foaming properties of regulators on the degree of oxyethylation have been determined. Adsorption isotherms of sodium oleate on apatite and calcite in the presence of regulators have been obtained. It has been shown that the presence of oxyethylated compounds in the solution reduces the amount of the adsorbed fatty acid collector. The influence of the considered classes of regulators on apatite flotation has been studied. The interrelation of flotation properties of oxyethylated compounds and their molecular structure has been established.INTRODUCTION Flotation plays a leading role in complex apatite-containing ores processing. However, two calcium-containing minerals - apatite and calcite, which compose apatite-carbonate ores, are characterized by close flotation properties. Selective separation of these minerals is a difficult task, the solution of which is impossible without using reagents-regulators. One of the ways to ensure the selectivity of the flotation separation of calcium-containing minerals is the use of reagents-depressants such as sodium silicate, starch, cellulose derivatives, and others (Liu et al., 2016; Rao et al., 1989). Another method is the application of nonionic reagent regulators (Filippov et al., 2016; Filippova et al., 2014; Ignatkina, 2017), which contribute to the adsorption of the ion collector (Filippov and Filipova, 2006 Rao and Forssberg, 1997) and stability of formed froth (Sis and Chander, 2003)."

Jan 1, 2018

By Chris A. Fleming

"The ability to recover cyanide from gold plant tailings has been known almost as long as the cyanidation process has been practiced, but there has been little incentive to process tailings in this way in the past. With the development of technologies that make it possible to recover and recycle free or complexed cyanide directly from gold plant slurry tailings, which indicates, on paper at least, significant cost savings compared to cyanide destruction, coupled with the introduction of legislation to seriously limit the discharge of cyanide to the environment in most gold-producing regions of the world, many companies are evaluating the cyanide-recovery alternative.There is arguably an even more compelling reason for mining companies to consider cyanide recycling. With the growing storm of negative public opinion that the use of cyanide in the mining industry is attracting - following several highly publicized spills over the last couple of years - the time has come for the gold industry to demonstrate environmental diligence and stewardship in the use of this commodity that is so vital for their industry. There is no doubt that the widespread implementation of cyanide recycling will reduce the impact of the cyanidation process on the environment, both by reducing the risk of spills (with less cyanide being transported from manufacturing plants to gold mines), and by reducing the loading of toxic and nontoxic metals and ions in the tailings.This paper briefly discusses the pros and cons of the different processes that are available for the treatment of gold plant tailings to regenerate and recovery cyanide for recycling, and presents a techno-economic argument for the incorporation of this technology into many gold plant flowsheets today."

Jan 1, 2003

By J. H. Zhang

An atomic force microscope has been used to measure the forces acting between two silica and two rutile surfaces in the presence and absence of cationic surfactants, CnTACl (n = 12~18). The forces measured in the absence of surfactant can be fitted to the DLVO theory. At short separations, however, the silica surfaces exhibited repulsive hydration forces, while the rutile surfaces did not. On the other hand, the forces measured in the presence of the cationic surfactants show long-range attractions that are larger than the van der Waals forces. The long range attractions are the strongest at of the point of charge neutralization (p.c.n.), which decreases with increasing surfactant chain length. The possible origin of the long-range attraction has been tested in view of the charged-patch model of Miklavic et al. (1994). However, the sizes of the patches back-calculated from the model were much larger than those the patches (or hemi-micelles) determined experimentally and reported in the literature. It is, therefore, suggested that the long-range attractions observed in the present work are due to the structural response of the water molecules in the vicinity of hydrophobic surfaces.

Jan 1, 2014

By G. Y. Liu

The structure-activity relationships for four thionocarbamate collectors are discussed in this pa-per. These collector classes are alkyl alkyl thionocarbamates, allyl alkyl thionocarbamates, acyl al-kyl thionocarbamates and alkoxylcarbonyl alkyl thionocarbamates. The main emphasis will be to highlight the differences between collectors and their affinities for copper and iron sulfide minerals on the basis of data on electronic-structure properties obtained by vacuum and solution density functional calculations, flotation experiments and analysis measurements. The mechanism of interaction of these collectors with sulfide minerals is also discussed with perturbation theory. The theoretical study results indicate that acyl alkyl thionocarbamates and alkoxylcarbonyl alkyl thionocarbamates have best performance in these agents as flotation collectors with improved collecting power for copper sulfide minerals and excellent selectivity against iron sulfide minerals, which are consistent with the experimental data reported in the literature.

Jan 1, 2014

By L. J. Li, Q. Zhang, Z. H. Liu, Q. L. Chen

Phosphogypsum (PG) is an industrial waste from the production of phosphate fertilizer. The utilization of PG is restricted by its containing impurities, and the pretreatment is crucial to eliminating these impurities. The purpose of the research is to recycle pretreatment PG as raw material for preparation of a-calcium sulfate hemihydrate (a-HH) by salt solution method. The effect of pretreatment technologies of lime neutralization and washing on dehydration rate, phase composition and morphology evolution of a-HH were investigated by crystal water content analysis, XRD and SEM. Furthermore, the change of pH in the reaction process was also discussed in detail. The results show that the dehydration rate of conversion PG to a-HH increases and the corresponding induction period, crystal growth period and total time decrease with an increase in CaO dosage from 0.2% to 0.6%. In the presence of 0.4% CaO or 0.6% CaO, the a-HH presents a long hexagon-prism-shaped crystal with a purity of 94%, and the end face of a-HH presents polyhedron. The system pH sharply decreases with the reaction time under different CaO dosage, and the pH variation from the initial alkalinity to acidity. The main reason is that as the co-crystallized phosphorus dissolved and released HPO42-, and with the pH decreasing to 4-5, HPO42- transformed into H2PO4-. The dehydration rate of washing PG is lower than that of original PG. Compared with the original PG, a-HH with the larger width and smaller aspect ratio can be achieved from the pretreatment PG subjected to lime neutralization and washing, meanwhile the crystal surface is more smooth.

Jan 1, 2018

By V. A. Masloboev, A. V. Svetlov, D. V. Makarov

"The methods of heap leaching are considered to be the most promising for the low-grade copper-nickel raw materials. The article presents intensification capabilities of the process. Objects of research: the low-grade copper-nickel ores of Moncheplutone deposits (Moroshkovoye Lake, Nyud Terrasa, Nittis-Kumuzh’ya-Travyanaya (NKT), as well as the copper-nickel ore dressing tailings of the “Kola MMC” JSC. The following directions for the intensification of the low-grade copper-nickel raw materials heap leaching have been considered: preliminary electric pulse destruction (EPD) of ore; ore crushing and further sulfuric acid agglomeration. The impact of sulfuric acid concentration (1-3%) on the extraction of non-ferrous metals kinetics from the copper-nickel ore dressing tailings under various conditions of the percolation leaching has been studied. INTRODUCTION The low-grade grade sulfide ores at the abandoned and producing deposits, overburden rocks, mill tailings and non-ferrous slag are thought to be one of the large-scale sources for non-ferrous metals, on the one hand. On the other hand, they are known to be the subjects of emergency environmental danger. For this reason, the use of mine dumps and tailings, as well as the remained ores left in the ground as raw products, and at the same time decreasing the load on environment, are considered to be the pressing ecological and economic issue (Chanturia et al., 2012). Methods of heap hydrometallurgical and bacterial leaching are sure to be potentially productive for processing such low-grade and technogenic raw materials (Petersen, 2016). The early studies of hydrometallurgical method possibility to process copper-nickel ores of the Murmansk region deposits were launched in the seventies of the previous century (Golovko et al., 1978). For referencing purposes, the main types of impregnated ores from the deposits Zhdanovskoye, Kaula, Sopchinsky Plast and Lovnoozerskoye were selected. The metal content varied, as %: 0.46-1.49 of nickel, 0.01-0.62 of copper. In the first experiments, the solution containing 150g/l of H2SO4 and 135g/l of NaCl, was used in the capacity of leaching reagent. The possibility of underground metals leaching from the ores of the Lovnoozerskoye deposit was justified due to the performed laboratory and further large-sized tests."

Jan 1, 2018

By Lev Malytin, Alexander Dyachenko, Roman Kraydenko

"A new method of processing beryllium raw materials based on interaction of beryllium mineral with ammonium fluoride was developed. Possibility of extracting ammonium tetrafluoroberyllate from bertrandite and phenakite minerals is proved. The developed technology allows replacing the outdated sulfate technology developed by Materion Corporation. INTRODUCTION Beryllium is a strategic metal, which is produced only in three countries: the USA, China and Kazakhstan. The world production of beryllium amounts to only 300 tons per year. More than 75% of the world beryllium production is manufactured from oxide beryllium ores in the USA by Materion Corporation. In Russia there is a large-scale beryllium ore deposit «Ermakovskoye» containig over 1 million ton of ore. Concentration of beryllium in ore amounts to 1,2%. Since the mineral base of ore is calcium fluoride, the sulfate technology of Materion Corporation cannot be used. After alloying and sulphuric acid leaching the fluorine-ion found in fluorite and beryllium together evolve into the aqueous phase. At the stage of Be(OH) precipitation fluoride-ion prevents complete isolation of beryllium into the phase of hydroxide, which increases the loss of beryllium. A new ammonium-fluoride method for processing high-fluoride beryllium ores has been developed at Tomsk Polytechnic University. The ammonium-fluoride method involves fusion of ammonium fluoride (NH4HF2) with a beryllium concentrate. The concentrate containing 10% of beryllium oxide and 25% of calcium fluoride is produced by flotation from the ore of Ermakovskoe deposit. The main component of the ore concentrate is fluorite CaF2, which does not react with NH4HF2. Beryllium in this concentrate is represented by two minerals: phenakite Be2(SiO4)2 and bertrandite Be4[Si2O7](OH)2. Ammonium fluoride, unlike sulfuric acid, does not react with calcium fluoride and is not consumed for decomposing the mineral base of the concentrate. Ammonium fluoride is an accessible and environmentally safe reagent, worth up to $ 1,200 per ton. The total amount of ammonium fluoride is recycled and is used for decomposing a new batch of beryllium concentrate."

Jan 1, 2018