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By Jun Li

Rate processes of silver cyanidation were studied with the objective of understanding the reaction mechanism. The research was divided into three sections: anodic dissolution of silver in cyanide solutions, cathodic reduction of oxygen on silver surfaces and the direct leaching of silver in oxygenated cyanide solutions. The charge transfer steps plus the diffusion of reactants from bulk solutions to the silver surface were identified as rate-limiting and the rates of both anodic and cathodic reactions can be calculated using the Butler-Volmer equation and Fick's first law. Based on mixed potential theory and the results of electrochemical studies, a comparison of the rate obtained from direct leaching with that predicted from the calculation is made. Calculated results agree well with the experimental data.

Jan 1, 1992

By Peijia Lin

Wheat straw was chemically modified by alkaline treatment followed by succinylation and sodium carbonate treatment for the use of cadmium and nickel adsorbent. The adsorption efficiency was calculated in different conditions. The experimental parameters were solution pH, adsorbent dosage, contact time and initial metal concentrations. The biosorbent was analysed by FTIR (Fourier- Transform Infrared Spectroscopy) to investigate the changes of surface functional group. The maximum adsorption percentages of cadmium (>99%) and nickel (>98%) were achieved using 5 g/L adsorbent with 50 mg/L initial metal concentrations. The adsorption kinetic study showed that the reaction was pseudo-second order kinetics and the adsorption isotherm was well fit by the Langmuir adsorption model. The dynamic column study indicates that modified adsorbent has a better adsorption capacity towards cadmium than nickel.

By M. Kobayashi, Y. Nishisu

"Fine multicomponent particles of yttrium and europium were synthesized through the precipitation from homogeneous solution, and the various characteristics related with the fluorescence were investigated. The morphology and the fluorescent characteristics of the synthesized particles were affected by ionic species in the stock solution. In the presence of sulfate ion, some parts of the precipitated particles were aggregated, and _the fluorescent characteristics were not good. On the other hand, in the presence of chloride ion or nitrate ion, the particles precipitated were almost monodispersed, and, the intensity of the fluorescent emission were strong after calcination. Further, these particles were also very attractive as the red phosphor in the mercury-free fluorescent systems.Introduction Eu doped Y oxide particles have been widely investigated for the application to the fluorescent lamps and displays: Recently, the fluorescent lamps are pointed as harmful electric equipments because of using mercury for excitation. Therefore, the use of the mercury in the fluorescent- system will be limited or prohibited worldwide in near future. Then, the development of the mercury-free fluorescent lamp is strongly required without delay. Inert gas such as neon and/or xenon seem to be applicable as new excitation element that replaces the mercury. However, in case xenon the excitation wavelength,' 146 and 172nm, is different from that of the mercury, 254nm, and then, the commercial phosphors which are used in the present fluorescent lamp system are not available. Therefore, the invention of the novel phosphors is essential for the development of the mercury-free fluorescent lamp. Further, the controls of the size and shape of the particles precipitated are also important, because the homogeneity of the size and the shape is very important for the fabrication of the layer of the phosphor particles. That is to say, the development of the phosphor particles with controlled components, size and shape is essential. The precise control of size and shape improves the packing density, and so, the screen performance of the lamp [1]. In addition, these phosphor particles should be also useful for the application of the flat-plane displays, for example, PDP, etc. [2,3]. In the present work, first, the particles including yttrium and europium for the precursor for red phosphor were prepared through precipitation from homogeneous solution. This process was precisely controlled for the control of the components, size and shape of the particles precipitated. Next, the particles precipitated were calcined, and then, their fluorescent properties were characterized. As a result, some of them showed the possibly available characteristics as the red phosphor for mercury-free fluorescent lamp system. These experimental results are presented in this paper."

Jan 1, 2000

By Pertti Koukkari, Nagendra Tripathi, Karri Penttilä, Justin Salminen

A computational fluid dynamic model for a novel flash ironmaking process based on the direct gaseous reduction of iron oxide concentrates is presented. The model solves the threedimensional governing equations including both gas-phase and gas-solid reaction kinetics. The turbulence-chemistry interaction in the gas-phase is modeled by the eddy dissipation concept incorporating chemical kinetics. The particle cloud model is used to track the particle phase in a Lagrangian framework. A nucleation and growth kinetics rate expression is adopted to calculate the reduction rate of magnetite concentrate particles. Benchmark experiments reported in the literature for a nonreacting swirling gas jet and a nonpremixed hydrogen jet flame were simulated for validation. The model predictions showed good agreement with measurements in terms of gas velocity, gas temperature and species concentrations. The relevance of the computational model for the analysis of a bench reactor operation and the design of an industrialpilot plant is discussed.

Jan 1, 2014

By Chang Wei, Zhigan Deng, Yizhao WANG, Cunxiong Li, Gang Fan, Xingbin Li

During the process of hematite precipitation, the transformation of Na jarosite convert into hematite has been studied in a batch reactor at different temperatures, ranging from 170°C to 200°C with 3h of the retention time in the presence of 30g/L Fe ( ) and 4g/L Na+. The composition of precipitation was seriously depended on the temperature, at 170°C hematite and sodium jarosite are the reaction products of iron precipitate, with an increasing in reaction temperature the sodium, sulfur content in precipitated decreased and sulfur mainly exist in forms of SO4 2-, and when temperature over 200°C hematite was the only phase in product. An increasing temperature was not only beneficial to iron precipitation, also conducive to jarosite conversion to form high quality hematite precipitate.

Jan 1, 2016

By William Gregg

Recent environmental and workplace safety legislation has Imposed more stringent limits on the amount and type of particulate emitted Into the air. In the past, the mass of particles contained In a volume of air was the governing criteria. Now the size and precise chemical nature of the particulate must be known and controlled In addition to it's ?mass. Processors of metallic materials have to implement stricter control practices and more efficient control equipment to meet the new regulations. Pulse-Jet dust collector systems are being used to control particulate emissions from various process gas streams. Pulse-jets :are also being used for maintaining a healthy environment In the workplace. this paper will discuss the impact of these regulations, the control techniques used to comply with such regulations, and the equipment needed for compliance.

Jan 1, 1992

By Toshihide Takenaka, Takashi Matsui, Nao Murakami, Masahiro Kawakami

"Electrowinning of Ti have been investigated in a LiF-NaF-KF melt including K2TiF6 at 773-923K by applying electrochemical oxidation ofH2 gas as an anodic reaction. The cathodic behavior of titanium and the anodic behavior of H2 gas were studied by voltammetry in detail to clarify the electrolytic condition for the process. The electrowinning of Ti was carried out by potentiostatic _electrolysis. Steady electrolysis was achieved under the suitable electrolytic condition without breaking out the anode effect. Titanium metal was electrodeposited on a Ti cathode though the deposits were usually powdery. It is concluded that this process is potential if the morphology of the deposit can be improved.IntroductionTitanium has such good properties as high specific strength and high corrosion resistance. However, the availability of Ti has been limited because the price of Ti is much higher than those of other common metals, such as Fe and Al. The production process of Ti ingot from its ore is rather intricate so that the production cost is high. If the simpler process is developed, the production cost should be retrenched. Titanium metal is usually produced by the Kroll process, which consists of the electrowinning of Mg metal in molten salt and the chemical reduction of TiCl.i by Mg metal. The Kroll process is very elabrate, but not simple. Because the chemical reduction ofTiCl4 by Mg metal is highly exothermic, a considerable amount of energy is wasted.Titanium metal can be electrowon in molten salt bath in principle. A simpler and more effective process than the Kroll process may be realized by the direct electrowinning so that the electrowinning of Ti metal has been studied widely[ 1]. Some researchs progressed to a pilot plant stages [2], but the electrowinning of Ti has not been industrialized yet."

Jan 1, 2000

By Junji Shibata

Extraction behavior of Ti(IV) and other metal ions, such as Fe(III), Fe(II), Cu(II), Zn(I1) and Co(I1) from acidic solutions like sulphuric acid and hydrochloric acid was studied in order to recover titanium from the waste solution in Ti02 production. Extractant used was tri-alkyl phosphine oxide whose trade name was Cyanex 923. Then, a study was made of the idea of simulating a countercurrent multistage extraction system, using the results of batch extraction. The simulation was camed out on extraction and saipping behavior for a Ti(1V)-H$O,-Cyanex 923 system. From the simulation result., the optimum operating condition of the system was considered.

Jan 1, 1994

By Satoshi Yamashita, Noboru Masuko

"Newly prepared bipolar membrane is promising to become a key material of an electrolyser for a production process of strong reducing solvent. This research is basic research for using bipolar membranes as electrolysers of reducing agents, Cr(II), TI(III) and V (II) on the laboratory scale. In this report, a bipolar membrane was tried with an electrolyser, reducing chromic chloride to chromous chloride. An analysis of mass balance demonstrates advantages of it over the former electrolyser equipped with an anion and/or. cation exchange membrane. The effects of current density and concentration of Cr(lll) on the reduction rate of Cr(II) and the current efficiency were examined No deterioration of the bipolar membrane resulted from the electrolytic reduction of Cr(III). IntroductionRecently, bipolar membrane that was the development subject for a long time in the industry of ion exchange membranes has met the stage of the practical application at last [l]. The expectation of the application to the hydrometallurgy field increases. We took up the manufacturing of the strong reducibility solvent as part of the application of bipolar membrane to hydrometallurgy technology. This laboratory has much experience in the electrolytic reduction of Cr (II) aqueous .solution such as chromous sulfateusing bipolar membrane were compared in theory to chromous chloride aqueous solution manufacturing of the strong reducibility solvent. The advantage of applying bipolar membrane by substituting ion exchange membrane is described, and the experimental result is reported."

Jan 1, 2000

Many studies have been conducted over the past 3 decades on the leaching of gold in solutions containing thiosulfate, ammonia and copper. However, most of these studies have been carried out using ore samples, with very few fundamental studies of this system being attempted. The majority of the published studies have failed to acknowledge the undesirable side reaction between copper(H) and thiosulfate, let alone account for its effect. The fact that the solution chemistry is constantly changing makes it very difficult to perform a fundamental study of gold leaching. With the advent of the rotating electrochemical quartz crystal microbalance (REQCM), such fundamental studies are possible as this instrument measures mass in real time. This has allowed leach kinetics to be measured in a matter of minutes and hence at essentially constant solution conditions; The present paper highlights that a sufficient concentration of copper(II) and ammonia are required in order to achieve appreciable gold leach rates. However, the use of air (oxygen) to maintain the copper(Il) concentration catalyses the undesirable copper(II) reaction with thiosulfate. The presence of ammonium ions is shown to have an effect on this undesirable reaction as well as on the gold leaching ?reaction. Preliminary electrochemical studies into .gold electrowinning using the REQCM show that gold(I) thiosulfate cannot be readily reduced to metallic gold in the potential region at which cementation usually occurs. However, it is well known that gold cementation onto copper occurs rapidly. The current study addresses this discrepancy by studying the effect that copper and silver have on the reduction of gold thiosulfate. It has been found that the presence of both silver and copper enhance gold deposition, particularly at low over potentials. While this is beneficial in cementation, the presence of copper and silver in solution has been found to cause passivation of the cathode surface during electrowinning at 'higher overpotentials.

Jan 1, 1998

By H. Masuda

The lijima Zinc Refinery started operation in 1972, and has today an annual capacity of 200, 000+-Zn. The hematite process was employed for the first time and the ideal of waste-free refinery has been pursued for 30 years. In recent years, however, only half of the hematite produced would be sold to the cement industry and hence a reduction of arsenic level has been necessary in order to sell the entire amount produced, The arsenic cementation process with zinc powder, developed through a long time laboratory research was found among some options as the best for the hematite process. The construction work started in 2000 and the facility was put into operation in 200 I. As a result in the same year all hematite were sold to the cement industry. The outline of this project, present operations and technical issue are reported in this paper.

Jan 1, 2003

By A. De, J. S. Zuback, T. Mukherjee, T. DebRoy

For successful commercial applications of additive manufacturing, metallic parts need to be defect free, structurally sound and reliable. However, additively manufactured metallic parts are susceptible to distortion, lack of fusion defects and compositional changes. Methods to measure susceptibilities of various alloys to these defects are needed but not currently available. Here we show that the necessary theories can be developed based on a well-tested numerical heat transfer and fluid flow model and decades of research in the field of welding. The proposed theories are validated with experimental results reported in the literature.

Jan 1, 2016

By Ligang Zhang, Wen Chen, Xinghua Liu, Jialin Li, Xiaoyin Liu, Zhenhong Liao

A research-scale fluidization and magnetization roasting device was developed to evaluate a processing option that might offset the complexity and high cost of the conventional magnetization roasting process on siderite. In this study, the operating parameters of the fluidization and magnetization roasting device for siderite were evaluated through cold-flow tests and magnetization roasting tests. The reaction mechanism functions of the fluidized roasting process are revealed with kinetic studies.

Jan 1, 2015

By Ana P. Paiva, Marc F. Comella, Sandra S. Reis, Joao N. Reis, M. Soledade Santos

"In this work, the influence of the malonamide structure, acidity of the aqueous phase and diluent on the equilibrium interfacial tension (IT) of N,N'-dimethyl-N,N'-diphenylmalonamide (DMDPHMA) and N,N'-dimethyl-N,N'-dicyclohexylmalonamide (DMDCHMA) in 1,2- dichloroethane (1,2-DCE), and DMDCHMA in toluene, with aqueous HCl, were investigated. IT isotherms were determined using the Du N ouy ring method. Densities of the organic phases were determined, and used to screen solute-diluent interactions. Formation of third phases was never observed; furthermore, ITs increase with the phase separation period, constant values being obtained for separation periods larger than 1000 seconds. Each malonamide interfacial efficiency at the oil/water interface is interpreted in terms of malonamide basicity, diluent polarity and malonamide - hydrochloric acid- diluent interfacial interactions.IntroductionFor several years now, N,N'-tetrasubstituted malonamide derivatives have been extensively investigated as liquid-liquid extraction agents since they were first proposed as the organic components of the DIAMEX process, with the aim of advantageously replacing tributylphosphate in PUREX [1]. Therefore, a significant part of research studies with malonamides appearing in the literature deal with the extraction of major and minor actinides in real or simulated spent nuclear fuels in nitric acid solutions [2]. Under typical experimental process conditions, the tendency shown by some N,N'-tetrasubstituted malonamide derivatives to aggregate in the organic phase, leading in a few cases to the formation of undesirable third phases, has been remarked and consequently thoroughly investigated [3, 4]. The increasing use of chloride streams as hydrometallurgical aqueous feeds is becoming a reality, and this fact is obviously deeply founded on an extensive research carried out to recover value-adding metals from these media. Following this trend, a number of N,N'-tetrasubstituted malonamides have already been screened for the recovery of iron(III) [5, 6] and platinum-group metals [7] from hydrochloric acid solutions. The results obtained are quite promising either in terms of total metal ion recoveries or selectivity patterns achieved. The formation of a third phase when iron(III) was extracted by the tested N,N'-tetrasubstituted malonamide derivatives has never been observed under the adopted experimental conditions, and the extraction data collected would need to be reinterpreted accordingly if any aggregation phenomena involving the considered extraction systems were to take place."

Jan 1, 2011

By Michael G. King

The primary non-ferrous metals industry is the principal supplier of the minor metals selenium, tellurium and bismuth. It is also a major supplier of antimony. These minor elements are recovered from by-products of base metals production. To ensure that these elements remain available, the cost of production must be compatible with four other factors - method of production, available supply, technological niches, and product stewardship. This paper first describes the relationship between the copper industry and the production of tellurium and selenium. The more complex relationship between the lead industry and bismuth production is then discussed, followed by comments on antimony availability. Product stewardship programs are essential to the growth or certain specialized markets for these metals. Smelters and refineries of non- ferrous metals will play a major role in the recycling of scraps and wastes from these markets. Examples on how such materials can be recycled are given in the paper.

Jan 1, 1995

By L. E. Murr

Preliminary studies of bacterial attachment to MoSp (molybdenite) have indicated a low correlation between dislocation density in the (0001) basal plane and the density of attached microbes. In the present investigation, poly- crystalline thin sections of CuFeSp (chalcopyrite) have been ion-etched or carefully comminuted to electron transparency and observed in the transmission electron microscope. The thinned test sections were then immersed in a culture solution in which bacterial attachment occurred. The attached bacteria were biologically stained in a uranyl acetate solution and the entire thin CuFeSp sections or tiny particles containing thin, electron transparent edges with bacteria attached were observed in the transmission electron microscope, allowing the coincidence of bacteria and their density to be directly observed in relation to lattice dislocations and crystallographic orientations of the exposed surfaces. This technique has the advantage of exposing crystallographic orientations where dislocation lines intersect the free mineral surface, and the emergence sites of dislocations could in principle be directly investigated as a possible preferential attachment site for bacteria. Bacteria morphologies were also extensively observed in the scanning electron microscope. The implications of the results are that although a strong correlation between dislocation density and distribution and bacterial attachment, density, and distribution has not been established, systematic multiplication of dislocation densities in crystalline mineral particles to be leached could enhance leaching rates by increasing the reaction rates as well as the density of attached bacteria at crystalline, metal-rich phases. Techniques for dislocation production in mineral and ore bodies and the particular implications in chalcopyrite leaching are discussed in relation to in-situ leaching where comminution is attained by explosives and the generation of strong shock waves in an ore body. The present study demonstrates the use of microanalytical and microscopic techniques in the investigation of fundamental microstructural phenomena in hydrometallurgical processes.

Jan 1, 1976

By A. Warczok

The oxidation and smelting of chalcopyrite, bomite, chalcozine and pyrite has been studied under simulated flash smelting conditions. The results of copper sulphide oxidation show that under constant oxidation conditions, the degree of oxidation drops sharply when the particle size is increased above a given range. This critical size range varies typically between 200 and 500 pm depending on the oxygen content in the gas phase. For bomite, chalcopyrite and pyrite, the critical size range increases with increasing iron content in the mineral and with increasing oxygen content in the gas phase. The extreme case is observed for pyrite in pure oxygen, where there is no effect of the particle size on the degree of oxidization. Microscopical observations of the oxidized products show the influence of different factors on the mechanism of oxidation and fragmentation of the sulphide particles. Based on microscopical analysis and phase identification of the oxidized products, a model has been proposed for the oxidation and smelting of copper sulphide particles in suspended state. The mathematical model describing the sulphide particle oxidation is supported by the obtained results. Using this model, it is possible to describe the role of particular factors in the sulphide minerals oxidation.

Jan 1, 1992

By E. Ilgar

"Deposition studies were conducted in acid copper electrolyte to determine the influence of chloride ions on cathode morphology. A statistically designed screening test was carried out in the absence and presence of 20 ppm CI- using a three factor, two level factorial design, in an electrolyte containing 36 gl'! Cu2+ and 150 gl-! H2S04, The independent variables evaluated were agitation; current density and temperature and their influence on surface roughness was determined. The copper deposited at current densities where activation was the primary control mechanism appeared similar in morphology whether stirring was used or not. The addition of 20 ppm CI- to the electrolyte gave rougher deposits under the same conditions. In the mixed control regions, considerably rougher, dendritic deposits were obtained when CI- was present. Agitation was effective in reducing the copper surface roughness both in the apparent activation and mixed control regions in the presence ofCI-. The results of this study showed that 20 ppm Cl- polarized the copper deposition at low overpotentials but caused depolarization at higher overpotentials.IntroductionChloride ion is inherently present in copper electrolyte, either as an additive or from other sources such as make up water. The behavior of the chloride ion is well documented in electrorefining operations, but its role in copper winning is less obvious. However in both cases there is evidence that cathode growth and solution chemistry are strongly influenced by its presence. The mechanism and electrochemical action of the Cl"" have been shown to be very complex, therefore a better understanding of its influence on electrocrystallization is essential for improved cathode deposit growth control. It was proposed that Cl"" polarizes the copper deposition reaction at low concentrations due to CuCI formation but depolarization occurs at higher concentrations due to the formation of a soluble CuCI2"" complex [1,2]. Franklin [3] reviewed the mechanism of additives in the electrodeposition process and proposed that the Cl"" complexed with copper, adsorbed on the cathode as an induced anion leading to an increase in the reduction rate. At cathodic overpotentials less than 100 mY, lppm NaCl had a polarizing effect, i.e. an increase in impedance of the charge transfer step. At higher Cl"" concentrations up to 100 ppm, depolarization occurred as evidenced by a decrease in impedance, which was attributed to soluble cuprous complexes [4]."

Jan 1, 1997

By Hiroaki Nakano, Kenji Hara, Shunsuke Kawano, Takeshi Ohgai, Michiaki Ikeda, Hisaaki Fukushima, Shinji Yamashita, Tetsuya Akiyama, Hisayuki Kaku

"Ni-Fe alloys have an inverse magnetostrictive effect (Villari effect) in which its permeability varies according to the ·applied strain. This alloy film has a potential for application as force sensors such as torque sensors, tension sensors and so on. Electrodeposition is promising as a technique for preparing Ni-Fe alloy film because of its convenience and economy. In this paper, the effects of electrolysis conditions on the magnetic properties of electrodeposited Ni-Fe alloy films were investigated. Hysteresis loops of Ni-Fe alloy films on copper substrates from sulfate bath were measured by a vibrating sample magnetometer (VSM). The films of low coercivity, which were preferred when used as a force sensor were obtained by introducing certain additives to the sulfate type bath.INTRODUCTIONNi-Fe alloys show an inverse magnetostrictive effect (Villari effect) that their permeability varies depending on the applied strain. The films of this alloy have a potential for application as force sensors such as torque sensors, tension sensors and so on. The authors et al. tried to prepare Ni-Fe alloy films using the sputtering technique, and produced a prototype of Ni-Fe alloy torque sensor [I]. The sensitivity was higher in the torque sensor thus produced than the strain gauge type one, and this torque sensor enables non-contacted detection. It showed excellent durability and reliability. However, the formation of Ni-Fe alloys by sputtering requires higher costs and brought an another problem that the shape of the substrate on which the film was formed was considerably limited. This causes a hindrance to the wide-range application of the force sensors. Electrodeposition is promising as the technique for preparing Ni-Fe alloy films because of its convenience and economy. In this paper, the effects of the conditions of electrodeposition on the magnetic properties of Ni-Fe alloy films were studied."

Jan 1, 2000

By Seshadri Seetharuman

The present paper summarises a series of measurements of the interaction parameter of oxygen in liquid copper with respect to a third element, e(M)o, where M is Mn, Zn, As, Se or Te which are common impurities in the liquid metal. The technique employed was the solid electrolyte galvanic cell method. The cell used may be represented as Pt, W or cermet / Cu-O-M // ZrO2 - CaO // AO, A /PT where AO/A represents a suitable oxide/metal reference. The measurements indicate that Mn and Zn interact very strongly with oxygen in liquid copper while, in the case of arsenic the interaction parameter is nearly zero. The behaviour of the elements Se and Te is unique with respect to oxygen interactions in copper bath. At oxygen levels, xo= 10-4 ? 10-5, the apparent interaction parameters are negative, comparable to that for sulphur. On the other hand, at lower oxygen levels, the results indicate that the interaction parameter values are positive. The results are discussed in the light of some of the theoretical models for solute interactions in liquid metals.

Jan 1, 1993