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By Varuzan Kevorkijan

A new method for faster production of functionally graded metal-ceramic laminates is based on reactive pressureless counterflow infiltration/penetration of a ceramic substrate with two different metallic infiltrants. The porous or dense ceramic preform is pressurelessly infiltrated or penetrated from one side by the first metallic infiltrant to the desired cross section of the preform, producing the top layer made up of the solidified infiltrant and the underlayer consisting of reactive infiltrated preform. The partly infiltrated preform is then completely infiltrated starting from the other side by the second metallic infiltrant, in this way fabricating the internal layer, consisting of the ceramic preform infiltrated with the second infiltrant and the bottom layer formed by the solidified second infiltrant. Systems already investigated include carbide, nitride and boride ceramic performs infiltrated with aluminum and magnesium alloys.

Jan 1, 2003

By Varuzan Kevorkijan

A new method for faster production of functionally graded metal-ceramic laminates is based on reactive pressureless counterflow infiltration/penetration of a ceramic substrate with two different metallic infiltrants. The porous or dense ceramic preform is pressurelessly infiltrated or penetrated from one side by the first metallic infiltrant to the desired cross section of the preform, producing the top layer made up of the solidified infiltrant and the underlayer consisting of reactive infiltrated preform. The partly infiltrated perform is then completely infiltrated starting from the other side by the second metallic infiltrant, in this way fabricating the internal layer, consisting of the ceramic perform infiltrated with the second infiltrant and the bottom layer formed by the solidified second infiltrant. Systems already investigated include carbide, nitride and boride ceramic performs infiltrated with aluminum and magnesium alloys.

Jan 1, 2003

By Timothy W. Ellis

"This paper presents the basic theory of operation, physical chemistry and phase equilibria which allow the development of liquid-liquid extraction circuits based on metallic solvents. The incorporation of reduction and reduction/diffusion processes into the process scheme is discussed and a detailed description of several liquid-liquid extraction schemes are developed. A synopsis of experimental results obtained using this method to separate rare earth and other metal based materials will be given.IntroductionConcerns over the effects of waste materials in the environment has been one of the significant social hallmarks of the late 20th century. Essentially every industrialized country has had to incorporate the cost of waste material into the equation of production. Legislative initiatives have led to the passing of very tough laws, by historical standards, which govern the environmental impact of materials processing.Liquid-Liquid extraction is a very common unit operation normally using aqueous and/or organic based solvents. Early work at the Ames Laboratory focused on the use of this technique for the reprocessing of spent fuel from liquid metal breeder reactors by the use of metallic solvents. Recently, we have revisited this area as a means to recycle/reprocess several emerging rare earth based materials, although this method has a much wider range of application. The reinvestigation of this technology is particularly timely as hydrometallurgical based processes are coming under increasing scrutiny in the U.S.A. by the Environmental Protection Agency (EPA). Although technology currently exists to remove contaminants from aqueous based waste streams, often the application of such methods is expensive. With proper design and judicious selection of reagents liquid metal extraction can achieve a high recovery along with a benign waste stream.This process has several possible advantages over other technologies. First is the elimination of aqueous solvents. Therefore, problems associated with disposal or reprocessing of the aqueous carrier are eliminated. Second, with proper system design, very high separation coefficients can be obtained thus limiting the number of stages required. Third, metals are extracted from metals with a metallic product, thereby eliminating the need to re-reduce metal for oxides or other compounds which are the common output for aqueous based extraction procedures."

Jan 1, 1996

By Jiangtao Li, Zhongwei Zhao, Xingyu Chen, Xuheng Liu

In order to produce good quality ammonium paratungstate, Sn needs be removed efficiently from the tungstate processing solution. The nascent hydrous ferric oxide has excellent adsorption ability and is often used as an adsorbent to remove metal ions from aqueous solution. In this paper, nascent hydrous ferric oxide is used to remove Sn from tungstate solution. Through experimental, the effects of pH value, reagent amount of adsorbent, reaction temperature and reaction time on the Sn removal are investigated. The study shows that 98% of Sn can be removed effectively from sodium tungstate solution and only 2% of W is lost during process under the conditions of pH 9~12, reagent amount of Fe addition 40 times Sn amount, reaction time 30min and room temperature. As the Fe addition reaches 90 times of Sn concentration in the ammonium tungstate solution, 99% of Sn is removed and APT with zero level purity national standard is obtained.

Jan 1, 2014

By Jiang Diao, Yong Qiao, Xuan Liu, Tao Zhang, Bing Xie

Adding CaO into the vanadium extraction converter is an effective way to decrease the dephosphorization burden in subsequent steelmaking process. The crystallisation process of spinel is one of the most decisive factors in the subsequent extraction. The theoretical calculation results show that the temperature of the peak total crystallization rate will decrease 5K with basicity increasing 0.1. The relation between cooling conditions and grain size of spinels is also discussed. It is found that low cooling rate and high basicity benefit spinel crystal growth. And the non-isothermal crystallization kinetics results indicated that the restriction factors of spinel growth is that solid crystals accept new components from liquid-solid interfacial. While the sample was cooled down to 1250 (1523K) at cooling rate of 5K/min, the crystal growth is consistent with Ostwald coarsening grew up law, and controlled by diffusion of particle.

Jan 1, 2016

By Jian Li, Guo Chen, Bingguo Liu, Hongying Xia, Jinhui Peng, Libo Zhang

"Decomposition of ammonium tetramolybdate to prepare Mo03 using silicon carbide crucible in microwave fields was investigated. The results were analyzed Using TG-DTG and X-ray diffraction. Meanwhile, the effects of heating rat, material thickness, socking time, socking temperature on the structure of preparing Mo03 were studied. TG-DTG curves show that the decomposition process of ammonium tetramolybdate is only one stage, in the temperature range 300-350°C, whose begin to decompose when temperature increases beyond 300°C. The molybdenum trioxide was prepared by thermal decomposition. The quality ofMo03 was not affected under the heating rat is 12°C/min. It was beneficial for decomposition ratio with the lower material thickness, longer soaking time, and higher soaking temperature. XRD curves showed that it is viable method for preparation of Mo03 by decomposition from ammonium tetramolybdate in microwave fields.IntroductionMolybdenum is widely used in national defense, aviation, industrial and agricultural production as rare refractory metal. Molybdenum trioxide is vital raw materials for the process of preparation of molybdenum. The traditional production technology of molybdenum oxide is that ammonium tetramolybdate is calcined in rotary kiln or 4-tube furnace [J,2J. But the longer production time, the higher production cost, the lower furnace thermal efficiency, and bigger the energy consumption, especially the powder is easy to leak, the working environment is poor by using rotary kiln [ 3 l _ The particle of molybdenum oxide is non-uniform by using 4-tube furnace because of the uneven temperature of every tube and the poor exhaust of boat bottom [4l _ However microwave heating is quick and uniformity, it is a meaningful research that the microwave is used in the process of calcining ammonium tetramolybdate."

Jan 1, 2013

By Shengqin Zhang, Yousef Mohassab, Feng Chen, Hong Yong Sohn, Mohamed Elzohiery, Amr Abdelghany

The kinetics of hematite concentrate reduction by mixtures of hydrogen and CO of various compositions has been investigated as part of the development of a flash ironmaking process at the University of Utah. This process produces iron directly from iron oxides concentrates by the gas-solid flash reaction based on the partial oxidation of natural gas, resulting in a significant reduction in energy consumption and greenhouse gas emission. The reduction kinetics of hematite concentrate of an average particle size 21.3 μm by the above mentioned gases in the temperature range 1423 to 1623 K (1150 to 1350 ºC) was investigated. Hematite concentrate particles can be reduced to > 90% by any of these reductants in several seconds of residence time typically available in a flash reactor. The activation energy ranged from 214 kJ/mol for hydrogen to 231 kJ/mol for CO.

Jan 1, 2016

By Antti Roine

Sulfidic zinc concentrates are usually roasted in a fluidized bed furnace into sulfur-free oxide form. Metallic zinc is produced from this oxidic calcine using hydrometallurgical leaching, solution purification and electrowinning stages. The roasting step is necessary because zinc oxides are easier to dissolve using traditional leaching methods than zinc sulfides. The Kokkola Zinc smelter uses various types of zinc concentrates and secondary materials as feed mixture. This makes it difficult to find optimum process parameters for the roaster when the composition and particle size distribution of the feed mixture varies even on a daily basis. Certain conditions may even cause difficult accretion problems or increase the amount of calcine in the process off-gas line excessively. A thermochemical heat and material balance model was developed for process advisor, in order to estimate the effects of different process parameters (temperature, process air coefficient, concentrate feed, oxygen enrichment, water feed, etc.) on the heat balance, roasting temperature and calcine composition. This model was constructed using the heat balance module of HSC Chemistry 4.0 software. The prevailing chemical compounds in the concentrate and calcine were verified using mineralogical analyses and equilibrium calculations. The roasting process seems to operate near chemical equilibrium conditions, if the behavior of the main components is considered. This paper describes briefly the basic principles of the calculation model and outlines the results with several diagrams and discussion. The calculated results were in reasonable agreement with the recent process air oxygen enrichment and water feed test campaigns carried out at Kokkola in 1999.

Jan 1, 2000

By Robert G. Telewiak

During the past few years, the international nickel industry has taken some important steps to respond to conditions of global production overcapacity, relatively flat demand and low prices. These include the implementation of major cost reduction programs by most producers, closure of some high cost operations and the establishment of the Nickel Development Institute. Consumption in the western world increased by about 7 per cent in 1987 compared to 1986, supplies were less than demand, inventories were low, and late in the year prices increased dramatically. By year-end 1987, most producers were operating at, or close to, their effective capacities. Nickel demand is expected to increase to the year 2000 at an annual rate of about 1.7 per cent, led by increasing usage in the stainless steel sector. If this rate of growth is realized, then there will be need for the effective capacity of the nickel industry to be increased. Producers in Canada have put considerable effort in the past few years into reducing costs - with impressive results. Mining costs, in particular, have been reduced dramatically. While production is still less than the peak years of the yearly 1970's, it has increased substantially from levels of the early 1980's. Over the next few years, production is expected to increase slowly. A key determinant of the level of production in the 1990's could be the effect that regulations on sulphur dioxide emissions have on limiting production.

Jan 1, 1988

By Guo Xueyi

The morphological characteristics of the nickel particles electrodeposited from chloride dominant aqueous solution was investigated. The effects of the electrolyte constituents, the parameters for the electro-deposition on the morphology of the nickel particles were addressed. It is evidenced that not only the particle size but also the morphology of the deposited nickel particles strongly depend on the electrolyte constituents and technical operation conditions. The electro-crystallization mechanism of the metallic nickel particles deposited at high current density was elucidated. The ultra-fine nickel particles with flake, nodular or dendrite shape may be produced by controlling the duration for electro-deposition.

Jan 1, 2003

By Kazuki Morita

A new route to produce solar grade silicon (SOG-Si 6N) from metallurgical grade (MG-Si 98%) has been developed in Japan, which may satisfy the increasing demand for solar cells in the near future. Since some elements such as P and B have very large segregation coefficients, solidification refining is not effective for their removal and costly processes, such as electron beam vacuum melting and oxidation plasma refining, are required. According to our previous results which showed the effectiveness of leaching procedure with Ca addition for Fe and Ti removal, possibility of P and B removal by acid leaching was focused expecting that their affinities for Ca in molten silicon might be considerable. Hence, the effects of Ca addition on the thennodynamic properties of P and B in molten silicon alloys have been investigated for overall control and optimization of the SOG-Si production process in the present study. The interaction parameters between Ca and P, and Ca and B were determined by chemical equilibration techniques at 1723 K. Although the interaction parameter between Ca and B was slightly negative, that between Ca and P showed a large negative value. Also, the results for the leaching test with various amount of Ca addition revealed that the removal fractions of both elements, especially P, drastically increased with increase in the Ca content, which showed very good agreement with the prediction from the interaction parameters derived in the present work. The present results suggest that the preliminary leaching procedure can reduce the processing time and energy for SOG-Si refining. Keywords: Silicon, Solar Cell, Refining, Acid Leaching, Thennodynamics. Interaction, Phosphorus, Boron, Calcium

Jan 1, 2003

By Pesic. Batric

A novel chitosan-pyridoxal-epichlorohydrin was synthesized and evaluated in our laboratories. The evaluation was achieved by performing kinetic and equilibrium studies of copper sorption. The parameters examined were pH, temperature, concentration of copper, particle size and selectivity of copper sorption against iron, zinc, cadmium and cobalt. It was found that pH was the most important parameter, and sorption of copper increased with pH increase in the range pH 2.5-6.0. The low activation energy of the sorption reaction, 1 1.13 kJ/mole (2.66 Kcal/mole), showed that temperature was not an important parameter. The synthesized chitosan was selective against iron, zinc, cadmium and cobalt. The selectivity with respect to last three metals was achieved by the kinetic difference of sorption, as sorption of copper was much faster than for other metals. Iron (Fe2+) does not adsorb on chitosan. The mechanism governing the sorption of copper is intraparticle diffusion. This finding was supported by the dependance of copper sorption on the square root of time, the low activation energy, and the fit of experimental data in the diffusion through the product layer equation.

Jan 1, 1994

By Lichao Ding, Jingbiao Fan, Yunnen Chen

"With the development of industrial production, more and more wastewater containing high concentration ammonia nitrogen was discharge into the environmemt, which caused serious harm to the environmemt. Treating the wastewater has great significance to protect water resources. Using air-stripping combined with oxidation to uptake high concentration of ammonia nitrogen wastewater. The influence of operating parameters was investigated. Experimental results revealed that pH of solution, aeration time and aeration strength showed heavy influence on ammonia nitrogen removal. Air-stripping combined with oxidation can be considered as an alternative approach for the removal of high concentration of ammonia nitrogen from practical metallurgical wastewater. When pH was 11, aeration time 20 min, aeration strength 1040 Lh-1, and oxidation with 10 % NaClO solution 10 min, the initial ammonia nitrogen 2130 mgr1 could reduce to 12 mgr1. Other items could also be removed to meet the ""Integrated wastewater discharge standard (GB8978-88)"".1. IntroductionThe rapid development of human activities has caused a worldwide increase of nitrogen in rivers, lakes and coastal waters. It leads to considerable eutrophication and an increase in the frequency of toxic algae blooms [1,2]. The concentrations of nitrogen in the water of China are pervading high [3]. The discharge of wastewater containing high concentration of ammonia nitrogen is one of the most important factors. Great efforts have been devoted to the removal of ammonia nitrogen from wastewater. Traditional methods include biological denitrication [ 4 ], chemical precipitation with magnesium ammonium phosphate [5], electrochemical conversion [6], air-stripping [7] and so on. Biological denitrication is the most common process in the treatment of ammonia nitrogen wastewater. But the process is only suitable for the removal of relatively low ammonia concentration due to the requirement of appropriate C/N ratio [8]. Chemical precipitation needs additional reagents, which may introduce new pollutants to water body. Electrochemical method often uses expensive metal or metal oxide as electrodes, and also consumes large quantity of energy [6].Although air-stripping makes use of stripping tower and consumes energy, it is very suitable for the removal of relatively high ammonia concentration. Different air-stripping conditions would appear different removal efficiency. And only air-stripping the effluent can not be attained the ""Integrated wastewater discharge standard (GB8978-88)"". In this study, we use air-stripping and oxidation to removal high concentration of ammonia nitrogen from simulated and real ammonia nitrogen wastewater."

Jan 1, 2011

By E. T. de Groot, D. L. Verhelst

With the successful start-up of Cominco's new KIVCET smelter, the final key component is now in place for Trail Operations to operate efficiently as a modern integrated zinc-lead facility. Unique metallurgical, operational, planning and management issues apply to this operation. Along with presenting the current flowsheet for Trail Operations, this paper discusses issues such as the impact of recycles, operational re-stabilization following significant process changes, plant operation with just-in-time inventories, real-time process optimization, and management philosophy.

Jan 1, 2000

By S. Gopalan, J. D. Milshtein, S. N. Basu

Production of syngas is proposed utilizing the W/W03 redox system and employing a solarpowered two-step thermochemical cycle. Three chemical reactions occur in two chambers. Assisted by a solar concentrator, a high temperature reaction reduces W03 powder to metallic tungsten in both chambers. Subsequently, the temperature in one of the chambers is lowered and H2(g) is produced via re-oxidation of the tungsten powder using steam. The temperature in the other chamber is simultaneously lowered to an intermediate temperature and CO(g) is produced via oxidation of the tungsten powder using C02(g)· The gas streams coming out of the two chambers result in the syngas production. A complete thermodynamic analysis of the system is described. The W/W03 redox cycle offers greater gravimetric fuel productivity compared to previously proposed systems, and the entire cycle can be operated below 1273K.

Jan 1, 2013

By Keith M. Axler

This report addresses issues specific to the generation of hydrogen fluoride via reaction of calcium fluoride with sulfuric acid. This process has been established on a commercial scale and is under consideration for treatment of calcium fluoride residues from uranium processing. Magnesium fluoride slags are also available as a product of uranium processing. The technique of using sulfuric acid for the production of hydrogen fluoride from magnesium fluoride is also under consideration as a residue processing scheme. In the current study, thermodynamic modeling was used to investigate these chemical processing systems. The results presented herein reveal information relevant to the selection of processing temperatures and conditions. Details include predicted effects in system composition based on operating temperatures for both the calcium fluoride and the magnesium fluoride systems.

Jan 1, 1996

By Dietmar Eifler, Marcus Klein, Hendrik Kramer

Conventional methods to characterize the fatigue behavior of metallic materials are very time and cost consuming. That is why the new short-time procedure PHYBALCHT was developed at the Institute of Materials Science and Engineering at the University of Kaiserslautern. This innovative method requires only a planar material surface to perform cyclic force-controlled hardness indentation tests. To characterize the cyclic elastic-plastic behavior of the test material the change of the force-indentation-depth-hysteresis is plotted versus the number of indentation cycles. In accordance to the plastic strain amplitude the indentation-depth width of the hysteresis loop is measured at half minimum force and is called plastic indentation-depth amplitude. Its change as a function of the number of cycles of indentation can be described by power-laws. One of these power-laws contains the hardening-exponentCHT eII, which correlates very well with the amount of cyclic hardening in conventional constant amplitude fatigue tests. To identify heat-treatment-parameters and SAE 52100 TRIP-alloys with high hardening rates as well as their damage tolerance the PHYBALCHT- and PHYBALLIT-method were used. One modified SAE 52100 TRIP-alloy was investigated in detail. The fatigue behavior and the cyclic hardening of the selected SAE 52100 TRIP-alloy was investigated and compared with conventional SAE 52100. Conventional stress-controlled fatigue tests were performed on a servo-hydraulic test system with a frequency of 5 Hz and a load ratio of R = -1. Different rates of cyclic hardening were identified. The size of the nonmetallic inclusions leading to crack initiation and the number of cycles to failure were used to evaluate differences in the damage tolerance capability.

Jan 1, 2015

Mineralogical and metallurgical scoping testwork were carried out to investigate the production of separate, marketable gold and platinum concentrates. The study utilized a flotation concentrate assaying approximately 5 wt% gold and 5 grams per tonne platinum. The gold-platinum mineralization was recovered from a placer deposit. Optical microscopy and scanning electron microscopy with energy dispersive x-ray analysis identified gold as zoned Au- Ag and Au-Ag-Cu alloys. Platinum primarily occurred as weakly zoned, variably magnetic Pt- Pd-Fe alloys. A combination of gravity and magnetic separations resulted in a gold concentrate grading 86.9 wt% Au (and 9.lwt% Ag) and a separate platinum concentrate grading 400 g/t Pt with recoveries of 94.5% and 96.7%, respectively. Magnetohydrostatic separation (MHS) using the Magstream 200 Separator indicated promising results.

Jan 1, 1994

By Alessandro Blasi, Massimo Morgana, Corradino Sposato, Pietro Garzone, Giuseppe Devincenzis

A comparison among (2-ethylhexyl)-mono (2-ethylhexyl) ester Phosphonic acid (P507), Secondary-octyl phenoxy acetic acid (CA-12) and Bis(2,4,4-trimethylpentyl) phosphinic acid (Cyanex272), in heavy rare earths separation via hydrometallurgical processes has been investigated. The separation coefficients, , were obtained and the extraction selectivity has been evaluated using a mixture of heavy rare earths from Samarium to Ytterbium. The experimental results indicated that P507 and Cyanex 272 display a greater affinity for heavier rare earths while CA12 proved to be more effective for the lighter rare earth metals.

Jan 1, 2014

By I. H. Gundiler

Sandia National Laboratories (SNL) is tasked to support The Department of Energy in the dismantlement and disposal of SNL designed weapon components. These components are sealed in a potting compound, and contain heavy metals, explosive, radioactive, and toxic materials. SNL developed a process to identify and remove the hazardous sub-components utilizing real-time radiography and abrasive water-jet cutting. The components were then crushed, granulated, screened, and separated into an aluminum and a precious-and-base-metals fraction using air-tables. Plastics were further cleaned for disposal as non-hazardous waste. New Mexico Bureau of Mines & Mineral Resources assisted SNL in investigation of size- reduction and separation technologies.

Jan 1, 1995