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By W. G. Wu

More and more researches and applications of organic chelating agents as depressors or activators are carried out in the course of research and application of modern flotation. The paper puts forward the necessary condition of organic chelating agents as depressors or activators by analyzing the chelating chemical performance of organic chelating agents with metal ions and the stability of chelates formed by them; at the same time, puts forward four sufficient conditions of organic chelating agents as depressors or activators according to different hydrophilic capability of the chelates and different performance of depression and activation of organic chelating agents for minerals. Namely, the ?1+1/4? necessary and sufficient conditions of organic chelating agents as depressors or activators are put forward.

Jan 1, 2014

By M. Blagojev, R. Tomanec

"Studies reported in this paper used polymetallic Pb-Zn-Sb-As-(Ag, Au) ore from Dražnja, Kosovo. The ore is comparatively rich in Zn (6.56%) and Pb (2.87%), but with high rates of Sb and As. Conventional lead and zinc concentration by flotation produced galena and sphalerite rich concentrate with high recovery, but with excessive As and Sb. After chemical analyses, which could not detect the reason for the excessive elements, ore minerals were identified under the ore microscope, their texture characterized, and degree of liberation of useful minerals was assessed. Microscopy of the mineral concentrates revealed complex intergrowths of galena and marmatite minerals mostly with sulphosalt minerals (boulangerite, jamesonite and bournonite) and also with arsenopyrite mainly responsible for the unsatisfactory quality of the concentrate. These complex sulphosalts, among other things have similar behaviour during the flotation concentration, and in spite of their interlocking with galena, therefore inadequate liberation, sulphosalts remain in the lead concentrate. Microscopic analyses indicated that a better galena concentration product is possible with a higher rate of mineral liberation, and then by selective floc flotation of some sulphosalt minerals. Purpose of this work was to show that only chemical analysis is not sufficient, according to that we solved the problem by precise mineral identification and time consuming mineral liberation measurements. INTRODUCTION The polymetallic Pb-Zn-Sb-As-(Ag, Au) ore body of Dražnja, Kosovo, fairly rich in Zn (6.56%) and Pb (2.87%) was repeatedly explored and once even worked. Mineralization at Draznja was primarily represented by sphalerite, galenite and marcasite/pirite. Some sections comprise massive sulphides, and others are lower grade zones of semi-massive sphalerite/galena or marcasite/pyrite dominant sulphides. The ore body II was formed in the southern gallery in the structure Çukë – Lajthishtë (with content of 3.16% Pb and 7.31% Zn). Pb-Zn ore with increased content of As, Sb sulphosalts is not rare phenomenon in the world. While previously treated as unprofitable, economical uninteresting ore, today with development processing and new reagents (organic, ecologic), are the topic of scientific papers. The examination of Pb-Zn ore with high content of sulphosalts we find in deposits as: The hydrothermal vein deposit of Harja in the Baia Mare area, contain a wide variety of sulphosalts [Cook, N. & Damian, G., 1997]; also the deposits Fankou Mine in Guangdong Province and the Dachang Mine in Guangxi Province, where the flotation concentration of galena and jamesonite takes place [Runqing Liu et al. 2015], [Zhang Ting, Qin Wen-Qing, 2015];. On a samples from Tibet in China flotation separation test of galena and jamesonite was conducted [Sun Wei, Han Haisheng, Tao Hongbiao, Liu Runqing, 2015]. According to history of investigation, the mineralized area of Dražnja has a long history of exploration and possible exploitation activities [Slowey, Galen, 2009]. Recent workings were carried out in three stages through the 20th century."

Jan 1, 2018

By E. Guerrini, M. Maccagni, J. Nielsen

"Lead is the most important material able to meet the current demand for energy storage. The lead acid battery is reliable, efficient and inexpensive. Continuous developments in battery construction are providing improvements in all aspects of the batteries’ performance. The lead acid battery is both the main lead product and the main raw material for lead production. More than half of the lead produced is from secondary smelters where batteries are the most important feed material. The environmental pressure on lead production has been increasing for many years, and continues to become stronger and stronger. The lead production processes and technologies themselves will require updating to meet the new regulations. Although they are very strict now, they will become even more so and current technologies may not be sufficient. Because recyclability is a strong point for the lead acid battery, the secondary smelters need to reduce the environmental impact as much as possible. In recent years, the secondary smelters underwent impressive changes in this direction, but some more improvements are possible. Electrochemistry can offer a step change improvement in making secondary lead production more environmentally friendly. Engitec has developed an electrochemical process base on a very high current density (high productivity) cell using an inexpensive electrolyte and at a relatively low cost. In this paper, the latest update on the technology is provided. INTRODUCTION The lead acid battery is considered the “walking dead” by some new technologies trying to replace it. It has played and will continue to play a very important role in our lives because it is inexpensive, fully recyclable and the existing lead and the mine reserves guaranty enough material for the extended future. According to the life cycle, the lead acid battery is the cheapest and the most effective system to store energy. Lead is practically a close loop where lead battery production consumes more than 80 % of the produced lead but contemporarily it is the most important raw material for the production of metallic lead. In fact, nowadays, the secondary production has overcome primary production and this trend is expected to continue. Primary lead is the make-up material for the existing battery production and the source of lead for the construction of the new ones."

Jan 1, 2018

By Xu Wang, Bang Chen, Xiujian Luo, Wei Tang, Xiao’ou Xia, Fangming Liu

"The inertia cone crusher has lots of advantages, such as big crushing ratio, fine particle size, material layer crushing, good passing tramp iron performance and stable technical index, realized open crushing circuit and simplified crushing flowsheet. The crusher was input to China’s Beijing General Research Institute of Mining and Metallurgy (BGRIMM) from Russia’s Mekhanobr-Tekhnika Research & Engineering Corporation at the beginning of the 1990s. This paper introduces that after years of absorption and innovation how Chinese researchers optimized and creatively designed about transmission mechanism, bracing structure, kinetic parameters, lubrication system, dust sealing system, damping system and hydraulic control system etc on the basis of keeping its advanced theory and unique structure, therefore the crusher’s stability was raised and the usage cost was reduced greatly. Accordingly the inertia cone crusher in China has been widely used in many fields, such as mineral resources and the recycling of metallurgical slag. The achievement in cooperation was fully affirmed by governments of Russia and China, and cooperation of science and technology in the mining and metallurgy industry between Russia and China is promoted greatly. INTRODUCTION From the early 1950s, the former Mekhanobr Institite(now Mechanobr-Tekhnika Research & Engineering Corporation) devoted itself to the research of inertial cone crusher and put it into industrial application in the late 1980s. Inertial cone crusher is like a maverick flower in the field of crusher. With its excellent performance and excellent application effect, it shocks the world and is destined to shine with a bright future. In the early 1990s, the chief leaders of the Beijing General Research Institute of Mining and Metallurgy (BGRIMM), Academician Sun Chuan-yao and Professor Zheng Baochen, captured the extraordinary performance and strong vitality of inertial cone crusher with keen eyes. So the two big institutes started the cooperation to introduce inertial cone crusher to China. Since then, Inertia cone crusher has been able to flourish in China and have achieved impressive results with two institutes’ continuous effort."

Jan 1, 2018

By A. E. Sobolev

The kinetics of hydrochemical oxidation of antimonite in solutions of nitric acid was studied using the rotating disk method and the factor experiment design. The dependences of the antimonite?s oxidation rate on concentration of nitric acid solutions, temperature, disk rotation frequency, and duration of interaction were determined. The adequate kinetic models allowing calculating the specific oxidation rate at any combination of the values of the influencing factors were obtained. The oxidation process is found to proceed in a mixed mode, close to chemically controlled. Gradually, as the sediments of elemental sulphur and Sb2O5 accumulate on the disk surface, the process becomes controlled by internal diffusion. The observed high (more than second) order of the oxidation rate with respect to the concentration of nitric acid was explained by the autocatalytic action of the acid reduction products. The apparent activation energy depends on the stage of interaction. At the initial stage (in a mixed mode of the process proceeding), it depends on nitric acid concentration and varies from 31.5 kJ?mol?1 (in 2 M HNO3) to 36.1 kJ?mol?1 (in 10 M HNO3). This trend indicates the weakening of diffusion limitations with a nitric acid concentration increase. When the process is controlled by internal diffusion, the apparent activation energy was found to be 14.5 kJ?mol?1. The obtained kinetic characteristics enlarge the database on hydrochemical oxidation kinetics of sulphides and can be used for the elaboration of the recommendations for the effective comprehensive exploitation of antimony-bearing ores and concentrates.

Jan 1, 2014

By Pengbo Chu, James Finch

Bubbles around 1 mm diameter provide the high interfacial area for capture and transport of hydrophobic particles in flotation. The formation of such fine bubbles is commonly achieved by addition of frothers that appear to simultaneously retard coalescence and promote break-up. High inorganic salt content in process water can substitute for frother. In this work we focus on the action of salt (sodium chloride) on formation of bubbles by break-up. An experimental setup that isolates break-up from coalescence was employed. A pocket of air is exposed to controlled mechanical turbulence to produce single bubbles by the induced deformation of the air and the events imaged. The presence of salt is shown to produce smaller bubbles than in water alone. Comparison with a similar study on frothers is made. The argument is advanced that the presence of frother and salt creates surface tension gradients at the air/water interface which add to the mechanical energy of the deformation and break-up process.

Jan 1, 2014

By A. K. Mukherjee

In this apparatus closed sized particles are placed in a container and then fluidized by passing water through the load of particles. Water flow is adjusted to deposit particles in one or more layers depending on the specific gravity of each of the particles, after which the deposited particles are separated in portions of different specific gravity. The obtained portions represent different ore content of the closed sized fraction. The process is repeated for all other size fractions to generate washability curve of the feed. Three different types of iron ores and one coal sample are tested in this equipment. The theoretical yield-grade curve generated for iron ore feed is unique in absence of any such practice for ore minerals. Similar curve is generated for coal and it is compared with washability curve, an existing practice followed worldwide. This comparison validates the performance of the process and the equipment.

Sep 1, 2012

By P. Zarate, M. Peart, T. Bhambhani, D. R. Nagaraj

More than 50% of all the molybdenum produced in the world is a by-product of copper production. A bulk Cu-Mo concentrate is first produced, which is subsequently separated into Cu and Mo concentrates. The Cu-Mo separation circuits rely on the use of inorganic Cu sulfide depressants such as NaSH, Na2S, and Nokes, which are hazardous, and sometimes require very large dosages for effective depression. Synthetic polymeric depressants are safer and more efficient, and are now being used on the plant-scale. Data presented in this paper demonstrates that these polymeric depressants can replace 50-90% of all the NaSH in Cu-Mo separation at a fraction of the NaSH dosage. In this paper we provide an overview of the mechanistic and practical aspects of the Cu-Mo separation with inorganic depressants and polymeric depressants. Important practical aspects include depression dynamics (related to conditioning time and rate of depression), optimum pH for effective separation, the role of pH modifiers such as lime and NaOH, and the effect of flotation gas on the efficacy of the separation. Using nitrogen as flotation gas, the NaSH consumption can be reduced by up to 95% by using a small amount of polymeric depressant. The experiments with conditioning time demonstrate that there is a significant rate component to the depression mechanism with NaSH, which is absent for the polymeric depressant system. This has important implications in the effective use and application of the depressant. It is also demonstrated that the pH modifier type (NaOH or Ca(OH)2) has no significant effect on separation efficiency and Mo recovery (i.e. Ca2+ ions do not depress MoS2 in the Cu-Mo separation).

Jan 1, 2014

By N. Tsoni

The separation and recovery of fine and ultra-fine particles during the processing of mineral commodities by conventional separation methods is difficult and inefficient. This is due to the problems posed by the very small size of the mineral particles. The fine and ultra-fine mineral particles are either generated during size reduction processes or are necessitated by liberation size. This problem is expected to deteriorate, as deposits of even lower grade are processed. The inefficiency of the conventional separation methods with regards to the processing of very fine particles leads to the loss of considerable quantities of mineral commodities to the tailings. Novel methods and techniques as well combinations of known methods have been tested over the years. Among them, selective aggregation, along or in combination with flotation, has been given much attention. This study deals with the application of hydrophobic agglomeration as a separation method for very fine particles. The selected mineral system is magnesite/quartz, due to its sensitivity to physi-cochemical separation methods. The aim was the selective agglomeration of magnesite using sodium oleate. Tests on single minerals revealed that separation seems feasible and efficient. The parameters examined were: pH, quantity of sodium oleate, conditioning time, and, finally, settling time. Tests carried out on artificial mixtures of the two minerals, under various proportions, confirmed the results obtained from single mineral tests but they were slightly inferior. Finally, hydrophobic ag-glomeration tests were carried out on single and artificial mixtures of minerals using sodium oleate and petroleum as reagents. The results show that the addition of petroleum improves the results. In conclusion, hydrophobic agglomeration can be applied successfully even for fine particles of difficult-to-be-separated systems such as magnesite and quartz.

Jan 1, 2014

By J. A. Venter

Mineralogical studies indicate the Pt-Pd-Bi-Te class to react poorly on the flotation stimuli and indications are that these minerals are slow floaters. However, recent studies performed on a number of minerals from this class indicated strong interactions with potassium ethyl xanthate resulting in the formation of dixanthogen (only one of several xanthate species). The poor flotation response is not a result of poor interaction of xanthate with the surface. It is proposed that the oxidation products of sulfides in the process water interact with the PGM surface. To test this, the effect of thiosulfate (an important oxidation product of sulfides) was investigated by employing electrochemical measurements and FTIR spectroscopy. The electrochemical investigations indicate no strong effect of thiosulfate on the interaction of xanthate with the minerals surface as well as the reduction of oxygenthiosulfate is likely not responsible for the poor flotation response of these minerals in industrial plants.

Jan 1, 2014

By Jerzy A. Mielczarski

The separation of albites from quartz by flotation applying the conventional HF-methods is no longer acceptable from an environmental and health point of view. Therefore, the search for a new reagent scheme without using HF depressor for separation of albite from quartz is under consideration. The flotation behaviour of ore mineral components depends on the produced hydrophobic or hydrophilic surface coverage (chemical functionalization). Currently we have excellent possibility of monitoring surface composition and structure at molecular and atomic levels at surfaces of natural minerals contacted with aqueous solutions of collectors, activators, depressants which is vitally important for the understanding of the surface chemistry that govern selective and efficient flotation. Detailed surface characterization of minerals before and after their exposition to different solution conditions was performed by the most modern spectroscopic techniques such as developed by us the infrared external reflection technique combined with spectral simulation and X-ray photoelectron spectroscopy (XPS). It is possible to monitor surface reactions which facilitate the separation process and those which bring disadvantage to selective flotation. At first we found that a small amount of ?mineral impurity? presented in natural ore could play important role in selective hydrophobization process. It was found that the pH of solution (parameter possible to control) and natural mineral impurities present in mineral samples (parameter related to ore origin) play a very important role in the separation process. Another important parameter is interaction between minerals, quartz and albite, present in aqueous solution. The limitation of flotation separation resulting from chemistry will be discussed. Moreover, the most promising scheme for separation of albites from quartz will be examined.

Jan 1, 2014

By W. H. Cheung

Nickel and cobalt production relies heavily on the processing of nickel laterite ores; these ores contain the majority of known Ni and Co reserves, 80% and 90% ~ 95%, respectively. The Caron process is used to extract Ni and Co metals from low-grade nickel laterite ores (1% Ni and 0.1% Co). It involves selective reduction of NiO and CoO minerals followed by ammoniacal leaching. Despite low metal recoveries, this process continues to be technically and economically reliable and thus commercially important globally. However, keeping the Caron process cost-effective has been a challenge for industries because of increasing economic and environmental pressures. Although studies of the Caron process have been extensive, significant improvements in recoveries of industrial processes have not been forthcoming. Reported industrial metal recovery from high iron content ore is only 80% ~ 85% for Ni and only 40% ~ 45% for Co; recovery is even lower for ores rich in magnesium. The real difficulty here is that there is no complete understanding of and control over the complex series of reactions in the ore and in the leaching solution during processing. Achieving effective metal recoveries from the Caron will require control of the mineral transformations, which affect the activation of minerals by reduction. In this study, the effect of over-reduction was investigated, which superseded the effect of activation by lowering the activity of the minerals and thus metal dissolution. Reduction was carried out in a batch reduction apparatus with 1:1 and 1:2.5 CO/CO2 gas mixtures from temperatures of 500 ~ 700°C and residence times up to 60 minutes. The pre-reduced ores were leached using a standard ammoniacal leaching test. Thermodynamic analysis and possible effects of stable phase field on leaching was examined. The results suggest that control of over reduction effects are directly related to the mineral transformation and reduction conditions.

Jan 1, 2014

By I. A. S. Brum

Brazil has large reserves of coal (7 billion tons) located predominantly in the south of the country. Despite the relative ease of exploitation, these resources have been underestimated as a source of energy. Currently the country's strategic planning aims to minimize the gap between coal and resources traditionally used in the Brazilian energy matrix. In this scenario, the processing of Brazilian coal in columns flotation appears as a promising alternative, having been successful in mineral systems containing fine particles. This paper aims to study the overall process of column flotation for a specific Brazilian coal. The material used in this study consists of fine coal that is usually discarded as waste and deposited in the tailings dams. The objective is to recover carbonaceous matter and reduce the ash and contaminants grade. The variables analyzed were the influence of size particle, solids concentration in the pulp, the concentration of surfactants and frothers to be used. The first results showed that it is possible, from a feed with around 65% of ashes, to obtain products with approximately 35% ashes with mass recoveries about 40%. Concentrations of frother (pine oil) ranged from 50 g/t to 300 g/t and the collector (diesel oil) of 50 g/t to 200 g/t. Keywords: column flotation, coal, tailings, negative bias

Sep 1, 2012

With significant increase in steel output in the world the price of iron ores has been soaring recently. Especially, there is a strong demand for iron ores in China, leading to more attentions paid to developing low grade iron ores. In this paper mineralogy of nm-of-mine hematite ore was deter-mined, and coal-based direct reduction-magnetic concentration was successfully developed to beneficiate low grade hematite ore. Mineralogy analysis indicates that this hematite ore is a super fine refractory ore, with the main valuable mineral hematite being closely associated with quartz and distributing uniformly and mostly occurring within the size of 3~5J.lITI,leading to being difficult to beneficiate due to super fine hematite and only grading 28.83% Fetotal. This hematite ore failed to be effectively upgraded by traditional processes in trial tests, such as reverse flotation, gravity concentration, and magnetic separation, or the integration of the above processes. In contrast with adoption of the coal-based direct reduction-magnetic separation process, concentrate was produced with high iron grade and metallization degree in the present work, which provides a theoretical basis for utilization of low grade iron ores. By optimization of direct reduction conditions, such as reduction temperatures, duration and mass ratio of reductant coal to iron ore, the reduced ore with 93.72% metallization degree was prepared, and then three-stage grinding-magnetic separation of the reduced ore were conducted, the final concentrate was manufactured, assaying 69.54% Fetotal and 98.01 % metallization degree, and with low content of impurities. This iron concentrate with high metallization degree produced by this process is a superior burden for converter instead of blast furnace. This process is enviromnent friendly by directly making iron using coal and iron ores instead of coke, resulting in less emissions and low production cost.

Jan 1, 2014

By Klaus M. Hahn, Hermann Wotruba, Bernd G. Friedrich

"Due to an increasing demand for nickel and cobalt and the depletion of nickel sulphide deposits worldwide, the production of ferronickel from lateritic nickel ores becomes more significant. About 60 percent of nickel reserves are present in laterite deposits. Common production methods like acid leaching or smelting operations implicate high material and energy consumption. Physical processing methods are also not efficient, because of the fine microstructural intergrowth of the minerals carrying valuable elements such as nickel and cobalt. Due to the high energy consumption of metallurgical treatment of lateritic nickel ore (nickel grade: 0.8 - 3.0%, Co: 0.05 - 0.15%), the separation of waste material (about 75 - 85%) before the metallurgical treatment is desirable. Therefore, an alternative process has been developed, combining a pyro-metallurgical pre-treatment with selected mechanical processing methods. The developed process consisted of a selective pre-reduction and non-selective segregation of the contained metal phases in the first stage. By this, the properties of the metal carrying minerals were changed and could become subject to concentration by means of fine beneficiation processes afterwards. The parameters of the pre-reduction and segregation were varied and the pre-treated samples were examined concerning their efficiency of metalization grade and metal grain size. This paper describes the investigation of pre-treatment methods of a lateritic nickel ore. The pre-treatment and possible subsequent separation methods were examined with regard to the recovery of the valuable elements. Metalization grade was around 80% for both Ni and Co with metal phase grain sizes below 20 µm. Scanning electron microscopy revealed distribution of new metal phases not only on the reducing agent, but also on the “slag” material.INTRODUCTION Nickel laterites are characterized as strongly weathered regoliths with several zones containing reserves of nickel (Ni) and cobalt (Co). These laterites are formed on serpentinites and ultramafic rocks under climatic and/or tectonic conditions that have changed over time (Butt & Cluzel, 2013). The formation of Ni laterites is influenced by numerous geological and environmental factors. In general, there are three ore types named according to the dominant Ni hosting minerals: oxides, hydrous magnesia (Mg) silicates and clay silicates (Butt & Cluzel, 2013). The most Ni laterite deposits contain two of these ore types, usually an oxide zone and an either clay or Mg silicate zone. Distribution of these principal deposit types, their average Ni-bearing phases and mean Ni grade are shown in Table 1. A schematic profile of the different deposits based on the development on serpentized ultramafic rocks is given in Figure 1 (Butt & Cluzel, 2013)."

Jan 1, 2018

By W. S. Eu

Thermal treatment of mineral ores can initiate thermal phase transformations which can affect either their activation or deactivation, subsequently influencing their ability to dissolve in a leaching reagent. The formation of rutile and hematite from ilmenite minerals, for example, has been suggested to occur through a series of reduction and segregation reactions. This process has been used in beneficiating low-grade weathered ilmenite ores to higher grade rutile. Despite decades of re-search, the mechanism of this process is not well understood, because dissolved intermediates are poorly crystalline and are difficult to quantify, with the exception of the final rutile products. Previous studies have shown that disrupted intermediate phases, by thermal treatment, are most susceptible to reagent attack and can often demonstrate ?activation? effects. In this study, synchrotron based X-ray diffraction method was used to investigate in-situ and in real-time the transformation of ilmenite minerals to rutile and hematite during calcination. The rate of formation and disappearance of specific Bragg peaks during the reaction and thermal decomposition of the mineral were used to derive an understanding of the solid-state reactions. The effects of the mineral transformation were validated by laboratory based batch calcination and leaching in sulphuric acid. The results suggest that transformation of major mineral phases occurs within of specific window of operation and thermal treatment appears to influence the extent of activation and leachability of ilmenite minerals.

Jan 1, 2014

By O. L. Kachor, A. V. Bogdanov

"In 2015 in the frames of federal special-purpose program «National system of chemical and biosafety of Russian Federation (2009-2014)» Federal State Budget Educational Institution of Higher Education ""Irkutsk National Research Technical University” (further–INRTU) performed works aimed at disposal of accumulated arsenical residues at industrial site of the former Angarsk arsenical plant (AAP) processing arsenious ores from Svirsk town in Irkutsk region. The plant in 1934-1949 produced arsenic trioxide for the defence industry. Prior to starting the works on disposal of industrial pollution focus the total amount of cinders stored on 13 ha of industrial site of AAP was 156 900 tons with 1% average arsenic content. Close to the cinders there were also remains of industrial buildings and process equipment in the amount of 6 600 m3 that contained 150 tons of arsenic. Additional source of pollution at the industrial site of AAP is contaminated soil amounted to 48 000 tons. Proven reserves of gold and silver in the cinders were 6.1 and 47 g/t respectively. In 2015 the source of arsenious pollution was detoxificated according to mineral matrix technology and stored in a special landfill with separate stocking of gold-containing cinder and other arsenious residues. This technology of waste disposal specifies extraction of valuable metals from cinder in future. The similar case is with Vershino-Darasunsky settlement in Trans-Baikal Territory where the abandoned industrial site of the former arsenic plant is located in the central part of the settlement. The concentration of arsenic and valuable components can be compared to the concentration at AAP. Since 2016 the demand for removal of such industrial pollution sources is legislated due to amendments in Federal Law No. 7-FZ on environmental protection. It results in a real possibility to remove such dangerous industrial residues deposits as the one located in Vershino-Darasunsky settlement. INTRODUCTION In the frames of federal special-purpose program «National system of chemical and biosafety of Russian Federation (2009-2014)» as well as the Irkutsk region program “Environment protection in Irkutsk region"" for 2006-2015, INRTU performed the works aiming at disposal of accumulated environmental deprivation–arsenical residues from the former Angarsk arsenic plant (further - AAP) (Figure 1) on processing of arsenopyrite ores of Svirsk town in Irkutsk regionThe plant produced arsenic trioxidein 1934-1949."

Jan 1, 2018

By Agnieszka Surowiak, Tomasz Niedoba

The paper presents a way of determining relations between ash content in coal, particle size and particle density by means of regression, multidimensional Morgenstern distribution functions and kernel approximation. The three-dimensional random vector (D, ?, ?), where D is a random variable describing particle size, ? - random variable describing particle density and ? - random variable describing ash content, where function ?=?(d, ?) is obtained by means of regressive function. The multidimensional Morgenstern distribution functions and kernel estimators with the use of Gauss function were applied to approximate the functions f(d, ?, ?) and f1(d, ?). This approach is a new way of multidimensional description of grained materials such as coal and it also allows to evaluate material features more properly than the classical statistical approach. The results were verified statistically.

Jan 1, 2014

By Yimin Zhu

This paper introduces the sixteen mappings and rules of mineral flotation and the subgroup, period etc in periodic table of chemical element to provide mineral flotation workers to refer in theory and practice research. the nine mappings and rules of mineral flotation and the subgroup, period are Saline minerals including the first main groups and collectors of aliphatic acid and aliphatic amines, Minerals including the second main group elements and collector of aliphatic acid, Hydrated ion of the second main group elements and quartz flotation, The floatability of oxidized minerals including the four main group elements, Organic acid including the fifth main group elements and wolframe, tin flotation collectors, The floatability of sulfide minerals including the fifth main group elements, Inorganic compounds including the seventh main group elements and mineral flotation regulator, Oxidized minerals including the forth Subgroup elements and organic flotation agents with phosphorus and arsenic, Oxidized minerals including the fifth subgroup elements and organic floating agents including the fifth main group elements, Minerals including the first subgroup elements and CN-, Sulfide minerals including the second subgroup elements and CN-, The effect of the highest N-valency inorganic acids or salts including p area elements of the third period in mineral flotation, Oxidized minerals including transition elements of the forth period and 3# flocculating agent, The floatability of minerals including elements of the sixth period, Element area of generating compositions and the collecting theory of mineral flotation and so and. Keywords: mineral flotation, periodic table of chemical element, subgroup, period, regulator, coordination chemistry

Sep 1, 2012

By R. X. Li

The overall flow-sheet of producing chromium (III) sulfate is described in this paper. The suitable conditions of each process such as sintering, leaching, aluminum removal, reduction, and de-composition conditions were experimentally studied. The results show it is reasonable to produce chromium (III) sulfate with the flow-sheet pointed out in this research work. The final product is Cr2(SO4)3 solution contained 150~250g/L Cr.

Jan 1, 2014