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By Heng Yi

The salt lake brines that lithium is extracted from have high chloride levels making the brine very corrosive to stainless steel extraction column internals. This is a significant problem in column scale-up to industrial production. Two types of corrosion-resistant ceramic internals, the hybrid ceramic internal and ceramic plate, were designed and tested under pilot conditions for future industrial application in this field. The hydrodynamic results (Yi et al. Ind Eng Chem Res 56 (4):999–1007 (2016), [1]) show that holdup of hybrid ceramic internal is higher than that of ceramic plate by around 50%, while Sauter mean diameter when using the hybrid ceramic internal is smaller than when using the ceramic plate by around 30%. This results in a larger mass transfer area, hence better mass transfer efficiency for the hybrid ceramic internal. Axial dispersion and mass transfer parameters are also examined (Yi et al. Ind Eng Chem Res 56(11):2049–3058 (2017), [2]). The results show that the column with hybrid ceramic internals has 50% lower axial dispersion coefficient and 50% higher mass transfer coefficient, leading to higher mass transfer efficiency. The transfer unit height of the column using hybrid ceramic internals can be as low as 0.2 m, showing very good efficiency. This is promising for near-future applications. Two-phase computational fluid dynamics (CFD) models have been developed for the two columns with ANSYS FLUENT commercial software. CFD successfully predicts the higher holdup and lower axial dispersion coefficients for the hybrid sieve plate pulsed column as measured in the experiments, and the cause for the difference in performance has been explained with information from CFD.

By Min Zhu, Yu Ji, An-chao Ren

"After being welded in the weld plant, the 100-meter heavy rails with the specification of 60kg/m are found broken during the straightening process in four planes. Failure analysis is made using the optical microscope and SEM with the result showing that the broken rail contains the imperfection of protrusion which exists at the edge of rail foot, about 1 00mm away from the rail end. When the protrusion is peeled off by deseamer from rail surface, cold scratch is generated which causes the rail to be broken during the subsequent straightening process. By adjusting the roll diameter differences between top and bottom roll of universal finishing mill and the height of pass line, it is possible to maintain the rails flat when leaving the mill. This prevents the upsweep and downsweep phenomena and, thus, the imperfection of protrusion can be eliminated. IntroductionThe development of rail transit worldwide has entered into a new era since the 1960s. The hi-tech rail transit system has gradually gained recognition over the world. In particular, the emergence of new-type passenger trains represented by TGV of France, ICE of Germany and Shinkansen of Japan and heavy haul trains as well, has revealed the charming way and more prosperous future of the modern and hi-tech rail transit system to the people all over the world. It should be pointed out that rail transit system is still the most effective solution to traffic jams among urban cities and in the central cities during the 21 '1 century, especially high-speed railway and subway which take overwhelming advantages over air transport, marine transport and road transport in terms of high speed, high efficiency, safety, comfort, environment protection and high flow. With the trend of increasing speed and heavier load of trains, higher product quality of rails is demanded. The rails for passenger dedicated lines require high cleanness, high accuracy in size, high flatness, high surface quality and large size (100-meter fixed length). The rail quality has direct influence on the operating performance of rail and railway traffic safety. The 100-meter heavy rails with the specification of 60kg/m are broken subject to the straightening process in four planes after being welded in the weld plant. This paper analyzes the reason for rails being broken and provides the theoretical proof for determining the rolling process."

Jan 1, 2013

By De-qing Geng, Guang-liang Wu

The waste slag generated by the LF refining process of Q345B low alloy hot-rolled steel, still has some refining capabilities. If recycled, it can reduce environmental pollution, and save the economic costs. A research on melting Characteristics of Q345B steel LF refining waste slag was investigated by using orthogonal experimental method, and the effect laws of composition on that were analyzed. Through variance analysis and significance criterion, it is concluded that the optimum ingredient of the regenerated LF refining slag is 25%A12O3, 12%CaF2, 7%MgO and R= (CaO)/ (SiO2) =2.5. And the regression analysis is carried out by using SPSS software, to get the mathematical relationship between ingredient with high reliability and melting temperature of refining slag T=1451.3-6.25CaF2+2.36 R.

Jan 1, 2016

By David G. Dixon

From its first implementation for the recovery of gold from low-grade ores by cyanidation in the early 1970s, heap leaching has developed into a key hydrometallurgical technology, in conjunction with solvent extraction and electrowinning, for the recovery of base metals, including most notably copper from both oxides and secondary sulphides, and more recently, nickel and zinc. And, given recent advances in bioleaching with thermophilic microbes, the successful application of heap leaching technology to low-grade primary copper ores seems only a matter of time. However, with each new development, it becomes increasingly apparent that the successful application of heap leaching technology will ultimately depend on our having an ever more complete understanding of the fundamental processes underlying it. Much work has been done toward the development of this understanding, on many different fronts. In this paper, a critical overview of heap leach modeling work to date is presented in terms of the most important phenomena which occur during heap leaching, and potential directions for future work are discussed.

Jan 1, 2003

By Afrodite Ntziouni, Vassilia Kasselouri – Rigopoulou, Athanasia Kyritsi, Konstantinos N. Pistiolas, Stamatia Gavela, Konstantinos Kordatos, Lazaros Iliadis

"The present study deals with the production and characterization of rice husk ash (RHA) and its use in the synthesis of zeolite of type ZSM-5. Rice husk was combusted in various temperatures with aim to find the suitable conditions for the production of amorphous silica. The resulted amorphous silica ash was then utilized as a starting material for the synthesis of ZSM-5 zeolite using the low temperature and atmospheric pressure process. The method led successfully to the synthesis of highly siliceous zeolite of type ZSM-5. The produced material was characterized using x-ray diffraction (XRD) and scanning electron microscopy (SEM).IntroductionRice husk is a major by-product of the rice-milling industries and it is usually used as a fuel for steam generation due to its high calorific power. During its combustion, rice husk ash (RHA) is produced. Knowing that the annual rice world production is over 615 million tons (2005), thus resulting in a potential production of more than 22 million tons of RHA [1], it can be understood that the RHA disposal is a crucial issue towards the environmental protection. However, due to the high silica content, RHA can be used as an alternative cheap source of silica for many uses, including as filler in polymers [2], concrete [3] and synthesis of zeolites [4-7].The burning of rice husk in air results in the formation of RHA with content in SiO2 that varies from 87 to 97% depending on the burning conditions, the rice variety, the climate and the geographic area [8]. Some small amounts of inorganic impurities are always present in the ash along with unburned carbon. The unburned carbon can be removed from the ash by further heating treatments in high temperatures, but this usually leads to the crystallization of the amorphous silica to cristobalite and/or tridymite [9]. The crystallization of the contained silica of the ash is also occurred when the burning conditions of husk are uncontrolled [10]. This crystallization is a disadvantage towards the preparation of silicon based materials, because the silica ash is rendered inactive in its crystalline form [11]."

Jan 1, 2008

By J. M. Tourre

Recently, interest in rare earth based oxide powders for electronic applications has risen dramatically. Considerable research has been devoted to the chemical synthesis of these compounds to improve the control of physical and chemical characteristics of the powder. In most cases, a high degree of homogeneity, purity and reproducibility is necessary in order to obtain good application properties. The synthesis parameters can control particle size, surface area, and morphology as well as the degree of homogeneity and application properties. Rhone-Poulenc, a world leader in the production of separated Rare Earth chemicals has developed a flexible process to produce a wide variety of compounds. The different processes for the synthesis of YBa 2Cu 3 O 7 will be discussed and compared to the RP process in term of product quality, cost and flexibility.

Jan 1, 1992

By I. U. Onyenanu, C. E. Ilochonwu, E. I. Nwonye, C. O. Nwajagu

This work shows how pure silica was derived directly from rice husks ash (RHA) in different temperatures for reduction to Silicon (Si). The processes to form Si materials are usually complex, costly and energy-intensive. The silica in the ash undergoes structural transformations depending on the conditions of combustion. A high purity silica was produced at 650oC after burning the rice husk (RH) for up to 7 hours. The purity of the silica was determined by dissolving the RHA with alkali solution to form sodium silicate solution of pH 11.0. This was added to hydrochloric acid of pH 1.5 which lowered the pH of the solution to 4.0 to form silica gels. The silica gels produced were washed and dried to powder and then characterized using XRD and EDX techniques. This study was done to reduce energy waste and environmental pollution in Nigeria as silica is used to develop many materials.

Jan 1, 2015

By Laurentiu Nastac

"This paper describes the development and validation of a comprehensive multiscale modeling approach capable of predicting at the mesoscopic scale level the ingot solidification structure and solidification-related defects commonly occurring during the vacuum arc remelting (VAR) process. The approach consists of a coupling between a fully transient macroscopic code and a mesoscopic solidification structure code. The predictions from the multiscale model, including grain morphology and size, primary and secondary dendrite arm spacings, Laves and NbC phases, tendency for freckling and columnar-to-equiaxed transition, were validated against experimental measurements for a 20-inch diameter VAR alloy 718 ingots. The validated model was then used to investigate the effects of melting rate and ingot diameter on the solidification structure of VAR processed 718 ingots.IntroductionThe objective of this work was to develop a fully transient multiscale modeling approach to get an insight into the effect of processing parameters on the cast micro- and macro-structure during VAR processing. The developed model assists in achieving better control of the ingot solidification structure and to determine trends in the macrosegregation in these ingots. Another objective of this work was to analyze the transient effects of production rate and ingot size on the resultant ingot microstructures. This objective was met by first understanding the effects of the full range of processing parameters typically used in the VAR process. Processing parameters such as power input and heat extraction rate significantly influence the ingot liquid pool size and shape as well as the ingot structure, which in turn will greatly impacts the final ingot quality."

Jan 1, 2012

Copper and gangue mineralogy constitute the most critical parameters for the hydrometallurgical processing and cost-efficient extraction of copper. Minor changes in copper-, rock-, or alteration mineralogy can severely impact the comminution efficiency, curing, agglomeration, acid consumption, copper extraction and PLS impurity loading. Further, copper leach operations, particularly in the southwestern United States, are increasingly challenged by a combination of low grades and semi-refractory copper. This paper discusses the metallurgical and economical benefits of continuous mineralogical analyses in order to establish and operate a mineralogical data base in copper leach operations. Troubleshooting for copper extraction, integration of process mineralogy into production forecasting, and process optimization will be illustrated with operational experiences from Chile and the United States.

Jan 1, 1999

By Boris Arlyuk

The system of short term forecast of metal prices at LME is based on correlation between prices within the quarter forward and at the first place by economic parameters at the West, determining the consumption of metals. Such economic parameters are presented by data of indexes of Western World industrial production (WW IP), official data of IP and Dow Jones indexes at USA. For price forecast within the quarter forward (one day ahead, 3 day -65 days MA forward prices) are significant the changes of actual prices (official and close) at the past and the parameters of daily trade at LME at the past (futures turnover, open interest, LME stocks). It is developed subsystem of price forecast within the quarter forward based on analytical approach determining the relations between the participants of the market. It gives the opportunity to reduce the number of empirical coefficients at the model and receive good accuracy of forecast the MA prices and its direction at the future. Very important part of short term forecast is subsystem determining analytically the probability that the price forecasted for the next trading day will be the maximum or minimum daily price within the quarter forward. The thresholds probabilities are defined by identification the model at the past by maximal commercial efficiency. Such system was tested at the past at period since 2000 till 2005 and gives very high commercial results at operations on 1M forwards and hedging the sales of nonferrous metals traded at LME (primary aluminium, light alloys, nickel, copper, zinc, lead and tin).

Jan 1, 2006

By J. P. Ibáñez

The uptake of copper from extremely dilute aqueous solutions by alginate in the form of protonated dry alginate beads was investigated. Barium was used to cross link the alginate forming the beads. The effect of various experimental parameters such as pH and metal ions concentration on the uptake of copper were studied. The uptake was strongly dependent on the Cu-bearing solution pH up to a value of 4.5. A removal of 100% o was achieved when the initial concentration of copper was as low as 8.0 mg/L. The maximum uptake, i, e., the loading capacity, was found to be 167 mg of copper per g of beads. The mechanism governing the removal of copper was found to be ion exchange between protons of the alginate beads and cupric ions of the solution. For this ion exchange process a molar ratio, d[H+]/d[Cu2+], of 2.0 was determined. EPMA-EDX analysis of the Cu-loaded beads showed a uniform distribution of the ions throughout the structure of the alginate, regardless the solution pH. This may suggest that this sorbent material is a porous ion exchanger having high permeability and capacity. The uptake of copper and of the heavy metals cadmium and zinc by this sorbent is compared.

Jan 1, 1999

By Kazusuke Sato, Takahiro Uno, Koji Hoshino

"A novel Ni coating technique of Ni(OH)2 powders was developed to improve the positive-electrode performance· of the Ni-MH batteries. It was found out that Ni(OH)2 powder was reduced by N2H4 without any catalysts in an alkaline - solution at high temperatures. In result of observation of pH and potential changes in the solution during the reaction, it was found that the reduced species was HNio2- ion dissociated from Ni(OH)2 in the alkaline solution. The molar fraction of reduced Ni of the Ni(OH)2 was increased in proportion to the amount of added N2H4. At the small Ni fraction, a porous Ni layer was formed on the surface of Ni(OH)2 powder. Open cell tests were carried out with the paste type electrodes made of either the Ni coated Ni(OH)2 powder or non-coat powder, and cell performances were compared. In result, it was found that the Ni coating technique is effective on improvement in the utilization of Ni(OH); as a positive-electrode active material under high current densities.IntroductionNi-MH rechargeable battery is generally used for the power source of portable machines and electric vehicles because of its good performance at high energy density and. long term cyclical life as well as cleanness and good safety. Cell component materials have been improved respectively, and as concerns ·the positive-electrode reducing 'the internal resistance is a principal problem to improve the discharging performance at higher current densities.In recent years, improved Ni(OH)2 powders coated with conductive materials as NI. or CoOOH have been developed for the· positive-electrode active materials in order to· reduce the internal resistance of the electrode1)· 2) The Ni coated Ni(OH)2, however, is costly because it is fabricated by .the -non-electrode plate technique which needs a expensive precious ·metal catalyst as PdC12We found that Ni(OH)2 powder was reduced by N2H4 without any cryatalysts in an alkaline solution at high temperatures. After the treatment, Ni(OH)2 powder become gray color like Ni powder from light-green color; and. turned into a magnetic. In this study, the mechanism of the -reducing reaction was investigated to apply the reactions .to a novel Ni coating technique of Ni(OH)2 powders, · and the performance of the Ni coated Ni(OH)2 powder obtained by the reducing process was evaluated as an -positive-electrode active material of Ni-MH batteries."

Jan 1, 2000

By Alessandra Bonoli, Garfìm Marianna

"Construction and demolition waste (CDW) is no dangerous material resulting from construction, and demolition of houses, large building structures, roads, bridges, piers, and dams. It is possible to recycle these materials, to reduce environmental impacts, and to reuse them in construction sector. To evaluate in a correct way the possibility to reuse this material it is important to lead laboratory tests to assess the proprieties and quality characteristics. European, Italian and British ad hoc Committees had elaborated specific Standards, to evaluate Geometrical, Physical, and Chemical requirements of recycled materials. A research was carried on to define the guidelines for laboratory tests, their suggested values and quality standards. The Construction and Demolition Waste Construction and demolition waste (CDW) is no dangerous, uncontaminated material resulting from construction, renovation, repair, and demolition of houses, large building structures, roads, bridges, piers, and dams. CDW waste is made up of wood, steel, concrete, gypsum, masonry, railway ties, roofing materials, carpeting, insulation, plaster, metal, and asphalt, and all waste included in CER Code 17. In particular Demolition wastes are defined as materials resulting from the demolition, instead Construction wastes are defined as waste materials resulting during construction process or in pre-manufacturing construction industry. Environmental problems In a lot of cases Construction and Demolition Waste materials were discharged in landfills, these are filling up with CDW and others, and some of them will close in the near future. In addition, illegal dumping of CDW debris can result in future health risks, decreased property values, cleanup costs and enviromental problems. The typical environmental impacts generated by CDW dumps are: 1- Dust problem, which causes air pollution, as will as forming dirty areas. 2- Uncontrolled locations, that will encourage the disposal of other waste types with the usual construction wastes leading to an environmental disaster. 3- The degradation and deterioration of the coastal lands and the natural protectorates. 4- The loss of aesthetic features. 5- Occupation of large areas, causing extra hauling costs. Therefore, it is wise to find other alternatives, like reuse or recycling, other than landfilling CDW debris or illegal dumps, because a proper management and the reduction of CDW amount can save money, conserve resources, and preserve the environment."

Jan 1, 2008

By M. Kane, O&apos

Operators and designers require a comprehensive model to predict performance of heap leach piles and provide input of reliable and defensible data for economic modelling. A conceptual, theoretical, or numerical predictive model addressing the required metallurgical, geological, biological, and operational considerations should be developed within the framework of the hydraulic performance of the heap leach pile. It is generally agreed that segregation, compaction, and consolidation are physical aspects which significantly affect recovery and in general hydraulic performance. Hydraulic performance of heap leach piles can be described through the application of unsaturated zone hydrology. Unsaturated zone hydrology describes the flow and storage of moisture and oxygen in a porous medium under conditions where the pore water pressure is less than atmospheric. The porous material is "unsaturated" if an air phase, in addition to the water phase and solid material phase, is present. These conditions describe the operation of a copper heap leach pile. This paper will focus on developing an understanding of hydraulic performance in segregated heap leach material and demonstrating that unsaturated zone hydrology can be used as the framework to improve understanding and prediction of heap leach performance.

Jan 1, 1999

By Joo Hyun Park, Kyu Yeol Ko

The viscosity of the CaO-SiO2-xMnO-yCaF2 slags (C/S=1.0; x=10, 40%; y=0 to 15%) was measured to clarify the effect of CaF2 on the viscous flow of molten slags at high temperatures. Furthermore, the Raman spectra of the quenched glass samples were quantitatively analyzed to investigate the structural role of CaF2 in a depolymerization of silicate networks. The critical temperature of the slags abruptly increased at 15%CaF2, which was confirmed to originate from a crystallization of cuspidine using XRD analysis. The viscosity of the slags continuously decreased by CaF2 addition in the 10%MnO system, whereas the viscosity of the 40%MnO system was not significantly affected by CaF2 addition. The effect of CaF2 on the viscosity of the slags was quantitatively analyzed using micro-Raman spectra of quenched glass samples accompanying with a concept of silicate polymerization index, Q3/Q2 ratio. A polymerization index continuously decreased with increasing content of CaF2 in the 10%MnO system, whereas it was not affected by CaF2 in the 40%MnO system. Consequently, the bulk thermophysical property of the CaO-SiO2-MnO-CaF2 slags was quantitatively correlated to the structural information.

Jan 1, 2014

By S. Pirzada, P. R. Taylor

A reactor was designed and constructed to perform experiments on the generation of value added products using a plasma heat source. The engineering drawings were developed to include multiple sample ports for temperature and velocity measurements and view ports were designed to allow the Physics group to make optical measurements. Two methods for feeding solids into the system were developed and installed. Preliminary experiments were performed to characterize the system at various flow rates and power settings. Experiments were performed using zinc metal and oxygen to form zinc oxide. The particles that were generated were characterized chemically using atomic absorption and x-ray diffraction; and physically using scanning electron microscopy. The particles appear to be of value added size; but there is a tendency for the fine particles to adhere to one another forming agglomerates. Additional experimental work will continue the evaluation of the major parameters.

Jan 1, 1988

By Gerardo R. Alvear

The ability to efficiently remove impurities contained in concentrates is a key point to consider when selecting copper smelting technology for new plants or modernisation projects. Volatilisation of impurities such As and Sb should occur as early as possible in the process, and preferably in the smelting furnace, so that they do not impact on downstream unit operations. The ISASMELTTM process has been demonstrated to remove impurities efficiently, through high levels of volatilisation. This behaviour is promoted by attributes of the process such as the strong bath agitation, and the flexible nature of the process design, allowing the operator to choose the optimal matte grade for impurity partitioning, and the positive effect of the moisture content in the feed. This paper presents the distribution of minor elements in the copper ISASMELTTM furnace. Distribution impurities of As, Sb, Pb, Zn and Co observed in the ISASMELTTM furnace at Mount Isa Smelter are reported. Then, based on plant results and thermodynamic considerations, the potential application of ISASMELTTM technology for processing complex concentrates is discussed.

Jan 1, 2006

By Yasuhiro Konishi, Kazunari Mizoe

"This paper describes a new processing of ultrafine, magnetic ferrites from sulfuric acid pickling solution in steel industry. In the ferrite processing, the iron (II) in the pickling solution was first oxidized to iron (III) by using the acidophilic thennophile Acidianus brierleyi. The bio-oxidized pickling solution was treated with solvent extraction to separate the iron (III) into the organic solution of tertiary aliphatic monocarboxylic acid. After that, the carboxylate solutions of iron (III) and other metal (cobalt) were hydrolyzed and precipitated ultrafine particles of crystalline ferrites at l90°C and l. 3 MPa for 20 min.IntroductionHot-rolled steel sheet has always a layer of oxides on its surface. The oxide layer arises as scale in hot rolling processes in steel industry, and the scale consists of the three iron oxides such as hematite Fez03, magnetite Fep4, and wustite FeO. Pickling removes chemically the scale layer that adheres to the steel surface. For normal steels, pickling is carried out in 15-20% hydrochloric acid at 60-70°C or in 20-25% sulfuric acid at 95-100°C. When steel is pickled with sulfuric acid, the scale oxides dissolve to give iron (II) sulfate.Spent pickling solutions are hazardous wastes containing a large amount of dissolved iron (II) and sulfuric acid, e.g., about 40 kg/m3 of dissolved iron (II) at pH 0. In typical commercial processes, spent pickling solution is usually cooled evaporatively to 5°C, and then to 0°C to crystallize iron (II) sulfate as its heptahydrate. After the crystallization operation, the sulfuric acid can be reused in the pickling operation.In this paper we describes a new processing of ultrafine, magnetic ferrite from sulfuric acid pickling solution, in order to recover dissolved iron (II) in the form of a valuable product. In the ferrite processing, the iron (III) was first supplied by the microbial oxidation of iron (II) in the pickling solution, and then the biooxidized pickling solution was treated with solvent extraction to separate the iron (III) into the organic carboxylate solution. After that, the carboxylate solutions of iron (III) and other metal (cobalt) were precipitated crystalline ferrites under hydrothermal conditions."

Jan 1, 2000

By Thomas K. Chow

For the well-being of all living creatures and in response to green-environment policy from governments around the global, it is essential to reduce SO2 emissions from mining / smelters as well as other industrial facilities around the globe. However, often times, these SO2 containing flue gases and smelter flash gases also include oxygen and SO3, which complicate the SO2 removal process and technology. There are many novel technologies recently developed for removing SO2 from such gases. Most of these, however, have not yet commercially demonstrated that they are technically viable and economically feasible. Many of these novel processes also generate undesired byproducts, which themselves then need to be disposed of in a safe and cost effective manner. Fluor has developed the Fluor SOx Cleanup Process with a wide variety of process configurations to customize removal of the undesired flue gas constituents in a cost-effective manner. The process removes practically all SO2 in the form of salable elemental sulfur and also reduces CO emissions. Successful operation of major components of the Fluor SOx removal technologies has been demonstrated in many commercially operating units. Besides their technical viability and economic feasibility, Fluor SOx removal technologies do not generate any undesired byproducts or encounter SO2 associated corrosion issues. Moreover, these technologies produce high-purity, saleable elemental sulfur. This paper discusses the merits of the Fluor SOx removal technologies, their technical and cost advantages, their simplicity in design and operation, and their readiness for implementation.

Jan 1, 2006

By P. G. West-Sells

Recovery of gold from thiosulfate leachates can be accomplished by adsorption of the gold thiosulfate complex by a strong base resin. Two of the most significant impurities that can decrease this gold adsorption are tetrathionate and trithionate, which are produced as oxidation products of thiosulfate during gold leaching. This paper investigates gold adsorption on a strong base resin (Purolite A500C) as a function of the concentration of these impurities. It is shown that concentrations of tetrathionate and trithionate as low as 150 mg/L can decrease gold loading by an order of magnitude, and that of the two ions, tetrathionate has a stronger detrimental effect. The resin and solution gold concentration profiles were successfully fit using a Freundlich isotherm, which further shows the strong effect of tetrathionate. To counteract the decrease in gold adsorption by tetrathionate, a novel process was proposed. Sulfite was added to the solution to oxidize tetrathionate to trithionate, and a nitrogen blanket was added to ensure that no further oxidation of thiosulfate could take place. It is shown that by incorporating this process, gold adsorption was doubled from both synthetic and real gold thiosulfate leachates.

Jan 1, 2003