Search Documents

By Gjergj Dodbiba, Toyohisa Fujita, Takahiro Kikuchi, I-Chen Wu

"In order to separate molybdenum (Mo) from the high-level radioactive liquid waste (HLLW), Pb-Fe based adsorbents were synthesized. The adsorbents were precipitated by adding sodium hydroxide in mixture of 1 mol/L lead nitrate and 1 mol/L ferric nitrate aqueous solutions. Each precipitate was then filtered, dried and ground to obtain a fine powder, which has been used as an adsorbent. Two main parameters were considered when synthesizing the adsorbents, i.e. the pH value at precipitation of adsorbent precursor and the calcination temperature of Pb-Fe based adsorbent. Moreover, the structures of the synthesized adsorbents were investigated by means of an X-ray diffractometer.The experimental results indicated that the calcination temperature of the Pb-Fe based adsorbent has a great influence on adsorption capacity of the adsorbent for Mo. It was found that when the Pb-Fe based adsorbent was calcinated at 500 oC, the sorbed concentration of Mo was the highest.1. IntroductionThe high-level radioactive liquid waste (HLLW), arising from the reprocessing of nuclear fuel are generally immobilized in an alkali borosilicate glass matrix. Broadly speaking, alkali borosilicate glasses are the matrix of choice for the immobilization of the HLLW, since they permit vitrification of waste stream of variable composition, [1]. Within this frame, the incorporation of molybdenum (Mo) is of particular interest in the vitrification of HLLW. Molybdenum is know to have a low solubility in borosilicate glass compositions and its presence in excess results in the phase separation of a complex yellow molten salt during vitrification, [1]. The formation of so-called “yellow phase” material during the vitrification process is undesirable since it leads to the accelerated corrosion of the inconel crucible liners. Furthermore, the “yellow phase”, which is reported to contain also other fission products, is soluble in aqueous solution providing a potential route for the leaching of radionuclides from the vitrified waste, should it come into contact with water, [1]."

Jan 1, 2008

By Todd S. Fayram

The Gordonsville Operation of Pasminco US Inc. along with the Center for Advanced Mineral and Metallurgical Processing (CAMP) at Montana Tech studied, developed and implemented a pilot scale hydrometallurgical facility for the industrial recovery of germanium and gallium. This paper describes the joint testing and engineering program that culminated in this successful process.

Jan 1, 2003

By Patrick R. Atkins

Energy issues will have increasing impacts on decision making in all facets of society over the next few decades. Industrial users of energy and producers of products that affect energy use must be fully aware of the implications of their processes and products on the energy situation. This paper describes a model that has been developed for the aluminum industry that allows scenarios to be evaluated to gain improved understanding of possible implications for our businesses. A brief overview of the model is provided.

Jan 1, 2006

By V. A. Bryukvin

A hydroelectrochemical technology has been proposed and experimentally proven for processing metallic gold- and silver-containing concentrates on the basis of copper and copper alloys obtained as a result of preliminary physico-mechanical upgrading of electronic scrap. The proposed technology is based on hydroelectrochemical leaching of scrap using reversible electric current and diluted nitric acid solutions, containing complexing agents, permitting complete separation of gold from the nonferrous matrix without involving gold in the process, and dissolving copper, zinc, lead and tin virtually without any emission of nitrose gases.

Jan 1, 2006

By V. T. Taniguchi

A process for large scale chromatographic separations using a continuous chromatography technique is described. The process combines the advantages of large scale batch fixed column displacement chromatography with conventional analytical or elution continuous annular chromatography (CAC) to enable large scale displacement chromatography to be performed on a continuous basis (CDC). Such large scale, continuous displacement chromatography separations have not been reported in the literature. The process is demonstrated with the ion exchange separation of a binary lanthanide (Nd/Pr) mixture. The process is, however, applicable to any displacement chromatography separation that can be performed using conventional batch, fixed column chromatography.

Jan 1, 1989

By J. G. Peacey, P. Hancock, R. -Q. Li

A pyrometallurgical process for the direct recovery of zinc from zinc concentrates and zinc/iron residues has been proposed and tested extensively by Noranda. The process consists of smelting bone-dry zinc containing materials (sulfide concentrates and secondary zinc/iron materials) in a molten iron oxysulfide bath to volatilize metallic zinc into a SC^-free offgas. Sulfur contained in the feed materials is fixed as an iron oxysulfide matte for disposal. Thus, this process not only is capable of treating zinc sulfide concentrates and secondary zinc materials simultaneously, but also eliminates the need of sulfuric acid production. Detailed thermodynamic analysis and experimental test work are described in this paper.

Jan 1, 2000

By K. Watling

Vibrational spectra of surface and solution compounds formed during cyclic voltammetry of a gold electrode in a deoxygenated 0.01 mol dm-3 NaCN solution have been examined using surface-enhanced Raman scattering (SERS) spectroscopy. The presence of cyanide at the electrode surface was indicated by Raman bands characteristic of the carbon-nitrogen stretch, CN.. Chemisorption of cyanide on the gold surface was evidenced by the presence of vibrational modes due to gold-carbon stretching, AuC, and gold-carbon-nitrogen bending, AuCN. Prior to the disappearance of the surface cyanide stretch band, a limiting value of the CN was obtained, the same as the value reported for adsorbed cyanide. Effects upon the voltammetry and vibrational modes of surface species due to additions of silver and lead to the gold-cyanide system have been observed.

Jan 1, 2003

By Javier Antoñanzas, Juan Carlos Múgica, Lourdes Yurramendi

The gasification of wastes containing an organic fraction is usually performed at low-medium temperature using different kind of catalysts. The off gas obtained is a mixture of carbon oxides, mainly carbon monoxide, and hydrogen and can be used for different energetic applications. The main problem is the production of tars in the off gas that has to be separated from the valuable gas flow and, finally, treated separately. An interesting alternative is the partial or total treatment of organics at high temperature. In this case, the off gas contains a higher content of hydrogen and elemental carbon as particulate matter. The energetic source to obtain a temperature in the range of 1,000 - 1,200 ºC is obtained by a plasma torch. In order to make de process attractive, an important issue to be considered is to commercialize the carbon obtained for different industrial applications.

Jan 1, 2008

By M. Sadayappan

The grain refinement characteristics of four low-lead and lead-free copper base alloys for plumbing applications were investigated. These are leaded yellow brass (C85800). SeBiLOY III (C89550), silicon brasses (C87500 & C87800) and silicon bronzes (C87600 & C87610); Boron and zirconium were found to be the most effective .grain refiners for copper .alloys produced using the permanent mold cast processes. The study indicates that the type of grain refiner to be used is dependent on the alloy type, alloying constituents and their content. After grain refinement, hot tearing resistance of the alloys was improved but mechanical properties remained unaffected. Alloys refined with boron are prone to the formation of hard spots, which will have adverse effect on the surface quality of the castings during polishing and buffing.

Jan 1, 1999

By Ahmet Geveci

[Generally accepted formula related to sulfur slag-metal distribution ratio is given by the following equation: [ ] According to the above equation it can be deduced that sulfur distribution between slag and metal is governed mainly by metal composition (?s term), slag composition (slag basicity and in turn sulfide capacity), oxygen potential of the system (ao¬¬ term) and temperature(related to equilibrium constant, K). In this study, the results of ladle furnace operations conducted in Erdemir-Iron and Steel Works Co. (Turkey) in relation to sulfur removal, have been given. Typical ladle furnace slag analyses of 4937K quality steel have been presented. Activity coefficient of FetO,?FetO, have been calculated with the relation obtained fromthe literature. Activity calculations have been performed with the program written in Mathcad. The changes in activity of aFetO in the slag phase,, have also been studied in relation to the sulfur removal: The relation between % Decrease aFetO and %DeS (measured)have been investigated for 4937K runs and someother types of steel produced in the Erdemir Plant. Related to ladle operations %desulfurization defined as [(%Sinitial-%Sfinal)/S%initial]*100 values have been presented for different steel qualities.]

Jan 1, 2006

By G. S. Nus

Technology for treating man-made metal-containing raw materials in DC electric furnaces with polarization of the bottom phase (PDF furnaces) has been developed and proven on a semi-commercial scale. PDF furnaces permit processing of man-made raw materials, i.e. current and accumulated intermediate products with rather high contents of valuable metals (i.e. slags, sludge, residues, Waelz slag, etc.), as well as secondary raw materials and virtually any type of waste using an environmentally safe technique based on sublimation of volatile metals and transfer of non-volatile metals and sulfur into the bottom phase in the furnace. Processes developed on the basis of the use of PDF furnaces make it possible to take advantage on a full commercial scale of electrolysis of molten materials, including electrochemical reduction of metals, intensification of their settling into the bottom phase and sublimation of volatile components, as well as to significantly improve recoveries of nonferrous metals, resolve the problem of excessive accretion formation in slagging processes and substantially improve the environmental situation. The low-grade discard slag obtained can be utilized in the construction industry; in particular, slag can be added to the limestone feed for cement manufacture.

Jan 1, 2006

By Sylvie C. Bouffard

The need for a better understanding of the heap biooxidation pretreatment of pyritic refractory gold ores has prompted us to develop a rigorous mathematical model of the process. The hydrological structure of the model takes the form of lateral stagnant pores in contact with a uniformly distributed gas stream and connected to vertical plug flow channels, as suggested by the results of an independent study of column hydrology. A model of pyrite oxidation kinetics was derived based on electrochemical leaching theory and the results of potentiostatic stirred tank and column tests. The growth rates of attached and planktonic iron- and sulfur-oxidizing cells are modeled with separate Monod expressions over three separate temperature ranges corresponding to mesophiles, moderate thermophiles, and extreme thermophiles. Isothermal column tests validate the model simulations. Excellent fits of several leaching indicators (potential, extent of sulfide oxidation, iron concentration, cell numbers) reveal the rate-limiting step to shift from particle kinetics to oxygen gas/liquid mass transfer with increasing temperatures and pyrite head grades. Competition for oxygen between sulfur- and iron-oxidizing microorganisms lowers potentials and slows down pyrite oxidation. This modeling tool may assist engineers in the design and operation of heaps to give more complete gold liberation in a shorter time.

Jan 1, 2003

By M. I. Zinigrad

A model of an ideal associated solution is presented. This model takes into account the existence of complexes of various compositions, sizes and geometries and allows calculating thermodynamic properties and phase diagrams of binary alloys. The model has been used formerly to calculate thermodynamic parameters and the position of the liquidus line for binary eutectic systems and also those having a stable compound in the solid phase. In all the cases the model parameters were not adjusted rather estimated from melting temperatures of the components. The recent studies dealt with the influence of arbitrary-stoichiometry associates on the equilibrium thermodynamic properties of liquid alloys. The application of the model to eutectic systems and systems having an unlimited solubility in solid and liquid states close to liquidus has been considered. It was shown that if the difference in melting temperatures of the components was small, different types of fusibility diagrams were possible: eutectic diagrams, cigar-shaped diagrams or diagrams with upper or lower azeotropic points. Peritectic transformations could take place when the difference in melting temperatures of the components was large. The present work is devoted to calculation of phase diagrams and thermodynamic properties of binary systems on the basis of chrome.

Jan 1, 2006

By Torben L. Edens

Norddeutsche Affinerie is the largest copper producer in Europe. Two sites are in operation for the production of refined copper: primary copper production is located in Hamburg and secondary copper production in Lünen. A total of just under 560,000 tonnes of copper cathodes is produced annually at the two sites. Primary copper production using the flash smelter furnace has been in operation in Hamburg since 1972. Over the years, the capacity of the flash smelter has been increased in three expansion projects from 120,000 t to almost 500,000 t of anode copper p.a. The anode sector consisting of two anode furnaces and a 24 mould casting wheel still features just about the same equipment as in 1972. The paper describes the most important steps taken to optimise operation which have put NA in a position to cast meanwhile more than 500,000 t of anode copper annually with the two anode furnaces and 24 mould anode casting wheel.

Jan 1, 2006

By Yong Hack Lee

Electric Arc Furnace (EAF) dust is generated when scraps are treated in the electric arc furnace and usually classified as hazardous industrial waste in most countries. EAF dust usually contains 15 to 25% of zinc and 3% of lead. It is usually treated in rotary kiln (Waelz process) or landfilled after a solidification and stabilization treatment. Numerous methods have been proposed as the EAF dust treatment technology, but few of them are in operation as a commercial scale except the Waelz process. Korea Zinc performed a plant test in which 600 tons of EAF dust was treated using TSL (Top Submerged Lance) technology. The TSL technology is a low cost, proven technology for processing zinc-bearing residues. The EAF dust was first de-chlorinated and fed to the TSL furnace. Finally, clean slag satisfying toxicity criteria was generated and valuable metals such as zinc and lead were recovered as fume oxide. The fume oxide was de-halogenated by sodium carbonate and sent to zinc refinery to recover zinc and lead. The recovery of zinc and lead was 90% and 93%, respectively. Most of the dioxin in the EAF dust was discomposed so dioxin less than the Korean regulation limit was detected in the offgas, which proves that the TSL technology is the best solution to treat EAF dust.

Jan 1, 2006

By Chu Yong Cheng

Synergists can be used in solvent extraction to improve the selectivity of extractants for metals. Research work carried out by the SX group at the AJ Parker Cooperative Research Centre for Hydrometallurgy / CSIRO Minerals has shown that the pH isotherm of nickel with Versatic 10 was significantly lowered by the addition of the synergist Acorga CLX50. The paper discusses how this synergistic shift can be used to alleviate a gypsum formation problem at Bulong nickel laterite operation in Western Australia. Metal pH isotherms were obtained with Versatic 10 and synergist CLX50 using synthetic leach solutions. In terms of pH50, the extraction order of the metals with 0.5 M Versatic 10 alone was Cu > Zn > Ni > Co > Mn > Ca > Mg, whilst the extraction order with Versatic 10 and 20% by volume CLX50 was Cu > Ni Zn > Co > Mn > Ca > Mg with the pH50 (Mn-Co) significantlyincreased. This is significant because the isotherms of valuable metals Ni, Cu, Co and Zn shift more towards low pH than those of the waste metals Mn, Mg and Ca, resulting in a possible good separation of Ni, Cu, Co and Zn from Mn, Mg and Ca. The use of intermediate precipitation, solids/liquid separation and re-leach in the three Western Australian nickel plants make these processes complicated and costly in capital and operation. The research work carried by the SX groupat the AJ Parker Centre has led to the development of direct SX (DSX) processes to recover nickel and cobalt from leach solutions using synergistic organic systems. Semi-continuous tests with a BHP Billiton pilot plant leach solution showed that Ni and Co together with Zn and Cu were separated from the major impurities, Mn, Mg, Ca, and Cl, in the first SX circuit. The co-extracted impurities were easily scrubbed. After stripping, Ni and Co together with Zn and Cu were concentrated, resulting in a much smaller second SX circuit in the down stream processes.

Jan 1, 2003

By Yang Tian-zu

Sodium pyroantimonate which is widely used as the clarifier in the glass industry and as the synergist in anti-flaming industry respectively has a production history of about 30 years in China. At present there is the production capacity of about 20,000 tons per year in China and China is chief producer of sodium pyroantimonate. In this work the production processes adopted by the producers of China, the operation conditions and the product qualities of sodium pyroantimonate prepared by different preparation methods have been summarized, and on the basis of comparing the advantages and disadvantages for each process the most advanced method - the air-oxidation method was introduced in detail. The production processes of sodium pyroantimonate mainly include the method of oxidation by sodium nitrate, the oxidation method of hydrogen peroxide, the potash salt method, the chlorination method and the air-oxidation method etc. The method of oxidation by sodium nitrate in which the crude antimony oxide, sodium carbonate and sodium nitrate are separately used as the raw material, the flux agent and the oxidant, has the advantage of short and simple technological process, but low grade quality of sodium pyroantimonate and bringing about serious environmental pollution are the disadvantages and this method has been substituted by other methods. Sodium pyroantimonate can be directly prepared by the hydrogen peroxide oxidation method with the advantages of simple technological process, high grade quality of the product and little environmental pollution. High grade quality of sodium pyroantimonate can be also synthesized by the potash salt method, in which industrial antimony white, the hydrogen peroxide, potassium hydroxide and sodium hydroxide are applied as the starting material. The disadvantages of these two preparation methods are high production cost and high requirements on the raw materials. The chlorination method with the crude antimony oxide, hydrochloric acid and chlorine as the raw material has the advantages of low production cost and high grade quality of the product. However complex process, high requirement of anti-corrosion for the equipments and producing plenty of waste water limit its application. The air-oxidation method with stibnite/jamesonite concentrate, sodium sulfide, and sodium hydroxide as the raw material and atmosphere as the oxidant is a newly developed method and its advantages are low production cost and the complex raw material can be treated by this method and its disadvantage is that the quality of sodium pyroantimonate is lower than that prepared by the oxidation method of hydrogen peroxide and the potash salt method.

Jan 1, 2006

By Sundarrajm Suresh, Hrushikesh G. Pimpalgaonkar, Thiyagarajan Paramadayalan

In this paper, a model of a fuel cell system has been proposed to account for the membrane physics at the micro level which is coupled with the macroscopic flow and mass transport phenomena occurring in a single channel of a Polymer Electrode Membrane Fuel Cell (PEMFC) system. We have developed a novel approach to model the catalyst layer electrochemical processes in a Membrane Electrode Assembly (MEA) and coupled it with mass transport and fluid flow calculations at the channel level using STAR-CD commercial software. The predicted values of the cell voltage from this micro-macro model are validated with experimental data available in the literature. A sensitivity analysis has been carried out to study the effect of the design and operating parameters such as catalyst loading and initial temperature on the overall performance of the PEMFC. The results indicate that the cell voltage increases at higher platinum catalyst loading and is also independent of the choice of initial cell temperature.

Jan 1, 2012

By Corale L. Brierley

Bioheap leaching, commercially applied for secondary copper ores and agglomerates, is rapidly gaining popularity. Bioleaching of chalcopyrite concentrates is imminent. Copper bioheap leaching encompasses the bioleaching of acidified and agglomerated coarse, secondary copper ore, stacked on permanent or on/off pads. The stacked ore is irrigated with raffinate containing bacteria. LME-grade cathode copper is produced by SX/EW. Low capital and operating costs, rapid start-up, environmental benefits, operational simplicity and a good performance record make bioheap leaching an attractive technology. This paper looks at the state-of-the-art of copper bioheap leaching and chalcopyrite concentrate leaching, the risks, the benefits, costs, bioheap performance and the future prospects of copper bioleaching.

Jan 1, 1999

By Sun-Hee Cheong

This study sought to produce L(+)-calcium lactate using precipitated calcium carbonate as a starter culture composite of lactic acid bacteria in lactic acid fermentation. Specifically, precipitated calcium carbonate was synthesized by reacting calcium hydroxide with sodium carbonate in the previous study by the authors. Synthetic precipitated calcium carbonate was then used as the calcium source of lactic acid bacteria during the fermentation process. In general, precipitated calcium carbonate has low absorption rate in the human body. On the other hand, calcium lactate has high absorption rate; it is commonly used in food and drug industries as calcium additives in various foods such as cookies, beverages, bread, sauces, powdered milk, and fruit juice. Calcium lactate has two racemates, e.g., L(+)-lactate and D(-)-lactate. In particular, L(+)-lactate is known to be more soluble than D(-)-lactate and generally produced from lactose by homo-fermentative lactic acid bacteria such as Lactococcus spp., Lactobacillus plantarum, Lactobacillus casei, Lactobacillus curvatus, and Pediococcus spp. Thus, the characteristics of the pertinent lactic acid bacteria and optimal condition such as temperature, pH, precipitated calcium carbonate addition rate, and content of fermentation for increasing formation yield and purity were investigated. The findings suggested the possibility of manufacturing L(+)-calcium lactate using precipitated calcium carbonate as a calcium source with high value-added instead of commercial calcium lactate.

Jan 1, 2006